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  • Wiley-Blackwell  (21,397)
  • 1995-1999  (21,397)
  • 1999  (1,566)
  • 1998  (7,078)
  • 1996  (12,753)
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  • 1995-1999  (21,397)
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  • 1999  (1,566)
  • 1998  (7,078)
  • 1996  (12,753)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2147-2156 
    ISSN: 1434-1948
    Keywords: Tetrapodal pentadentate ligand ; Ligand periphery ; Polydentate amine complex ; Nickel ; Podand ; Schiff base ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The tetrapodal pentaamine ligand 2,6-bis(1′,3′-diamino-2′-methylprop-2′-yl)pyridine (1), which contains four equivalent primary amino groups, can be derivatised partly or completely by Schiff base condensation with suitable carbonyl compounds. The new ligands thus obtained are mononucleating, as shown by the X-ray crystal structures of their respective nickel(II) complexes. Reaction of 1 with 1 equiv. of salicylaldehyde and subsequent reduction allows the selective modification of one of the four sidearms. The resulting ligand 2 is hexadentate and uninegative in its nickel(II) complex {[(2)Ni]PF6} (3) with both the secondary amine and the phenoxide functionalities coordinated to the metal centre. The unreduced Schiff base form of the ligand, 4, does not form a complex with nickel(II) as readily, and only a small quantity of the mixed salt {[(4)Ni][(1)Ni(H2O)](Br)2(PF6)} (5)has been obtained. While the overall coordination of 4 resembles that of 2, there is considerably more strain in the appended chelate ring, due to the presence of the C=N double bond. Modification of one arm in 1 can also be achieved by condensation with 1 equiv. of acetylacetone, to give the new ligand 6 which, likewise, is hexadentate in its NiII complex {[(6)Ni](PF6)2} (7). In this case, however, the N/O-functional sidearm is not deprotonated. Rather, it is coordinated as the keto-imine tautomer, making 7 a rare example of a metal complex containing this structural fragment. Two-fold functionalisation of 1 is observed upon reaction with acetone, regardless of whether the ketone is present in stoichiometric amounts or in excess, to give the pentadentate ligand 8with two diagonally juxtaposed isopropylidene-imine units. The complex isolated with this ligand {[(8)Ni](PF6)2} (9) contains pentacoordinate NiII, the sixth coordination site being blocked by the rigidly positioned isopropylidene groups. When reacted with 4 equiv. of trans-cinnamaldehyde, all the primary amino groups in 1 condense to give the four-fold Schiff base 10, which acts as a pentadentate podand towards nickel(II). In this complex, {[(10)Ni(OH2)]Br2} (11), an aqua ligand completes the coordination octahedron. All ligands are stable towards hydrolysis when coordinated to the metal, despite the presence of alkyl-imine groups in some cases.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2157-2166 
    ISSN: 1434-1948
    Keywords: Septadentate N5S2-ligand ; Dinuclear complexes ; Nickel ; Reactivity ; Redox chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The coordination chemistry of a series of dinickel complexes of the new septadentate amine-thiolate ligand N,N′-bis[2-thio-3-aminomethyl-5-tert-butylbenzyl]diethylenetriamine, H29, has been investigated in the context of ligand binding and oxidation state changes. The complexes [Ni2(9)(L)][ClO4]2 (10), [Ni2(9)(Cl)][Cl] (11), [Ni2(9)(L)][BPh4]2 (12), and [Ni2(9)(NCS)][OH·OH2] (13) have central N2Ni(μ-SR)2NiN′3L cores [L = labile solvent molecule (10, 12), Cl- (11), and NCS- (13)] composed of dithiolate bridged planar NiN2S2 and six-coordinate NiN′3S2L units. This is demonstrated for 11 and 13 by crystal structure determinations and for 10 and 12 by UV/Vis spectroscopy and room temperature magnetic susceptibility measurements. Complexes 10, 11, or 12 readily add other co-ligands at the NiN′3S2L fragment by substitution of the solvent molecule L (10, 12) or the chloride substituent (11). The overall structure of the parent complexes is not affected by the substitution reactions. An electrochemical study has shown that complex 10 undergoes two successive one-electron oxidations at +0.88 and +0.41 V vs SCE. The oxidized species are not thermally stable, but electronic absorption spectra and EPR spectra are indicative of the presence of NiIII species.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2167-2172 
    ISSN: 1434-1948
    Keywords: Macrocyclic compounds ; Amine-Thiolate Donors ; Polynuclear Complexes ; Nickel ; Condensation reactions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel route to macrocyclic amine-thiophenolate ligands is described. The new, air-stable thiophenolate precursor 1,2-bis(4-tert-butyl-2,6-diformyl-phenylsulfanyl)ethane (4) is readily condensed with two equivalents of 1,2-ethanediamine or 1,3-propanediamine under medium to high dilution conditions to give 2 × 4 condensation products. The smaller 1 × 2 macrocyclic compounds are not produced under these conditions. Subsequent reduction with NaBH4 (reduction of imine groups) and Na/NH3 (reductive cleavage of aryl-alkylsulfides) provides the 36- and 40-membered amine-thiophenolate ligands H46a and H46b. The macrocyclic compounds are versatile ligands for the preparation of polynuclear transition metal complexes. With divalent nickel H46a forms the di- and tetranuclear complexes [Ni2(6a)] (7) and [Ni4(6a)][ClO4]4 (8). Reaction of 8 with four equivalents of NH4SCN yields the novel isothiocyanate complex [Ni4II(6a)(NCS)4]·10MeCN (9). The structure consists of well-separated molecules of the tetranuclear complex [NiII4(6a)(NCS)4] (Ci symmetry). Two symmetry-related binuclear [N2Ni(μ2-SR)2NiN4] fragments composed of thiolate-bridged distorted planar {N2S2Ni}- and distorted cis-octahedral {(SCN)2N2S2Ni} units reside within the cavity of the macrocycle. The intramolecular distance between the two binuclear units is 6.144(1) Å.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2173-2185 
    ISSN: 1434-1948
    Keywords: EPR spectroscopy ; Metallocenylboranes ; Organovanadium radicals ; Redox chemistry (CV) ; X-ray diffraction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The paramagnetic complexes di(mesityl)([5]trovacenyl)borane (5·), (mesityl)di([5]trovacenyl)borane (6··), and tri([5]trovacenyl)borane (7···) were prepared from [5]trovacenyllithium, (η5-C7H7)V(η5-C5H4Li), and (Mes)2BF, (Mes)BF2, and BF3, respectively. The propeller-shaped species 5·, 6··, and 7··· were subjected to X-ray diffraction with the aim of possibly correlating the twist angles with intramolecular intermetallic communication. Cyclic voltammetry points to successive vanadium-centered oxidation processes and boron-centered reduction, a small redox splitting δE1/2[(2+/+), (+/0)] being observed for 6··. According to EPR spectroscopy, performed in fluid solution, the exchange interaction J in the diradical 6·· approaches the fast-exchange region and is attenuated significantly by quaternization at boron in [6··-nBu]-. Although EPR spectroscopy of the triradical 7··· also indicates an extensive exchange interaction, the exchange parameters, derived from spectral simulation, follow the gradation J(7···) ≈ 1/3 J(6··). The magnetic susceptibility of 6·· and 7··· follows the same trend. As expected, compound 7··· exhibits spin frustration because it contains three antiferromagnetically coupled S = 1/2 systems that are arranged in an equilateral triangle.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2187-2199 
    ISSN: 1434-1948
    Keywords: Ansa compounds ; Cp-derived chelate ligands ; Neopentane chemistry ; Spiro compounds ; Tripodal ligands ; Cyclopentadienyl compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The neopentane-derived functionalized oxetane O(CH2)2C(CH3)(CH2OMs), 1, reacts with indenyllithium (LiInd) or fluorenyllithium (LiFlu) to produce the derivatives O(CH2)2C(CH3)(CH2R) (R = indenyl, fluorenyl), 2. The oxetane ring of 2 undergoes nucleophilic ring-opening by reaction with LiPR′2 to give the chiral chelate ligands (HOCH2)(CH3)C(CH2R)(CH2PR′2) (R = indenyl, fluorenyl), 5. Nucleophilic ring-opening by LiInd or LiFlu is possible too, resulting in the functionalized ansa-Cp ligands (HOCH2)(CH3)C(CH2R)(CH2R′) (R, R′ = indenyl, fluorenyl), 12. Electrophilic ring-opening of 2 with HBr to give (HOCH2)(CH3)C(CH2R)(CH2Br) (R = indenyl, fluorenyl), 3, is also possible. The alcohol function of 3 may be activated directly, whereas activation of this group in 5 is only possible after BH3 protection of the phosphane function. The mesylates (MsOCH2)(CH3)C(CH2R)(CH2Br) (R = indenyl, fluorenyl), 4, undergo, under basic conditions, spiro cyclization to produce spirocyclobutane derivatives 9 with the α-carbons of the five-membered cycles acting as the spiro centres. Substitution of the mesylate group of 4 by PR2 nucleophiles is therefore not possible. Ansa-Cp derivative (MsOCH2)(CH3)C(CH2Ind)(CH2Flu), 12c also reacts with LiPPh2 with spiro cyclization to produce 9d, instead of giving the substitution product. Tripodal ligands (CH3)C(CH2R)(CHPPh2)2 (R = indenyl, fluorenyl), 11, are accessible by the reaction of (MsOCH2)(CH3)C(CH2PPh2)2 with LiInd or LiFlu. All compounds are fully characterized by the usual spectroscopic and analytical techniques including single-crystal X-ray analyses in several cases.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2201-2207 
    ISSN: 1434-1948
    Keywords: Carboxylate syn-anti ; N-centered tripodal ligand ; Manganese ; Imidazole ; Helicoïdal inorganic chiral chain ; Magnetism ; π-π interaction ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of an infinite inorganic chain consisting of MnII and an N-centered tripodal ligand N,N-(2-pyridylmethyl)[(1-methylimidazol-2-yl)-methyl]glycinate is presented. It exhibits a chiral helical structure with a pitch of two monomeric units (each monomeric unit containing one Mn atom). Each manganese is connected to its neighbor through a carboxylate bridge in a syn-anti geometry. Around each manganese center, two carboxylates bind in a cis geometry. This peculiar bridging geometry (syn-anticis) provides a broken-line chain, running in a zig-zag manner along the b axis of the P21 space group. The magnetic properties have been investigated. They show a pseudo-2D magnetic structure, with one major pathway along the chain and an inter-chain minor one. The intrachain coupling is a weak antiferromagnetic interaction (J/k = -0.25). This low value is entirely consistent with the geometry of the bridge. The interchain coupling is a weaker antiferromagnetic coupling (J′/k = -0.11) and could be mediated through π-π interactions between pyridine and imidazole from two adjacent helixes.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2221-2231 
    ISSN: 1434-1948
    Keywords: Calixarenes ; Inclusion compounds ; Imido Complexes ; Molybdenum ; Tungsten ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses, spectroscopic properties, molecular structures, and bonding of novel calix[4]arene imido compounds are described. Treatment of M(NtBu)2(NHtBu)2Ia (M = Mo), Ib (M = W) or M(NMes)2Cl2(dme) IIa (M = Mo), IIb (M = W) (Mes = 2,4,6-Me3-C6H2) with p-tBu-calix[4]arene LH4 affords calix[4]arene metal complexes LM(NR) 1a, b (M = Mo, W; R = tBu) and 2a, b (M = Mo, W; R = Mes). Analytical and spectroscopic data are consistent with monomeric structures for 1 and 2, retaining a local C4v symmetry for the calix[4]arene metal fragment. These complexes are well-suited to bind small molecules like acetonitrile, tBu-isonitrile, or water within their macrocyclic pockets. The spectroscopic data of some inclusion compounds and the crystal structures of LMo(NtBu)(NCMe) 1a(NCMe), LW(NtBu)(OH2) 1b(OH2), LW(NtBu)(CNtBu) 1b(CNt Bu), LMo(NMes)(NCMe) 2a(NCMe), and LW(NMes)(NCMe) 2b(NCMe) are reported. All complexes contain a group VI metal imido [M=NR] moiety mounted on the phenoxide rim of the calix[4]arene ligand as well as an incorporated guest molecule within the cavity. Some insights into the structures of complexes of the type L′W(NR′) (L′ = p-H-calix[4]arene; R′ = H, Me) and into bonding in these compounds are provided by density functional theory, applying the B-P86 density functional and an all SVP basis set within the RI-J-DFT approximation. At least one π bond is of importance for calix[4]arene-metal bonding in these compounds. The metal-imido bond can be described as a triple bond. A geometrically optimized minimum structure of L′W(NMe) 4 shows a calix[4]arene ligand only slightly distorted from a local C4v symmetry and an almost linear tungsten-imido moiety.
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  • 8
    ISSN: 1434-1948
    Keywords: Arsonium salts ; Superacidic systems ; Structure elicidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of trimethylarsane in the superacidic systems hydrogen/fluoride antimony pentafluoride and hydrogen fluoride/arsenic pentafluoride leads to trimethylarsonium fluorometallates. These salts are stable up to 60 °C and 5 °C, respectively. Structures were successfully elucidated in the cases of trimethylarsonium undecafluorodiarsenate and trimethylarsonium hexafluoroantimonate. (CH3)3AsH+As2F11- crystallizes in the monoclinic space group P21/n with four formula units per unit cell with the dimensions a = 7.362(1), b = 12.589(1), c = 13.598(1) Å and β = 95.37(1)°. (CH3)3AsH+SbF6- crystallizes in the monoclinic space group P21/m with four formula units per unit cell with the dimensions a = 8.313(1), b = 8.855(1), c = 13.285(1) Å and β = 94.358(1)°.
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  • 9
    ISSN: 1434-1948
    Keywords: Molybdenum ; μ-Oxo ; Conformational equilibrium ; X-ray diffraction ; NMR spectroscopy ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new thiocyanatomolybdenum(VI) dioxo-μ-oxo complex dimer bearing a 4,4′-di-tert-butyl-2,2′-bipyridine ligand (2) is shown to exist in the crystal cell unit as a meso (Mo-O-Mo angle of 180°) and d,l, pair (Mo-O-Mo angle of 155.7°). These conformers are in equilibrium in solution and have been observed clearly by 1H NMR spectroscopy.
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  • 10
    ISSN: 1434-1948
    Keywords: Macrocycles ; Lithium ; Fluorescence ; Cryptands ; Coordination ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three aza-cages with the anthracene-containing photoactive groups L1, L2, and L3 have been synthesized. All compounds are able to selectively encapsulate a lithium ion and solid complexes have been isolated. The formation equilibria have been investigated by UV/Vis and 1H, 13C and 7Li NMR spectroscopic techniques. The fluorescence emission of both free ligands and lithium complexes have been investigated. Results indicate that the CHEF (chelation enhancement of the fluorescence) effect obtained by lithium coordination exits although lower than that occurring upon full protonation.
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  • 11
    ISSN: 1434-1948
    Keywords: Copper ; Trinuclear complexes ; Formamidines ; Magnetism ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Three new copper(II) linear trinuclear compounds are reported, all of which were synthesized in-situ, with the general formula [Cu3(L)4](CF3SO3)2(Y)x, where L is the dehydronated ligand: N,N′-bis(pyridine-2-yl)formamidine (abbreviated as Hpdf), N,N′-bis(pyrimidine-2-yl)formamidine (abbreviated as Hpmf) and N,N′-bis(5-methylpyridine-2-yl)formamidine (abbreviated as Hmpdf), Y = EtOH or H2O and x = 0.5-1.5. The compounds were characterized by X-ray diffraction, IR, LF, and EPR spectroscopy and by magnetic susceptibility down to 4 K. The structure of the compound [Cu3(pmf)4](CF3SO3)2(H2O)1/2 was determined by X-ray crystallography; it was found to crystallise in the triclinic space group P-1 with a = 8.529(5), b = 15.760(5), c = 19.639(5) Å, α = 101.793(5), β = 101.263(5), γ = 102.389(5)°, Z = 2. The structure [Cu-Cu-Cu angle 174.96(11)°] consists of four nearly flat molecules of the ligand, which contribute to the propeller-type structure around the Cu-Cu-Cu axis. A strong antiferromagnetic interaction between the CuII ions is observed with calculated J values, based on the Hamiltonian H = -2J(S1·S2 + S2·S3) - 2J′·S1·S3, of -174(1) cm-1, -120(1) cm-1, and -167(1) cm-1 for the compounds studied with L = pdf, pmf, and mpdf, respectively. These values are in agreement with an S = 1/2 ground state below temperatures of 120-160 K.
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2277-2281 
    ISSN: 1434-1948
    Keywords: Boron ; Iron ; Nickel ; Carbyne complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The μ3-boryloxycarbyne complexes [{Fe(CO)3}3{μ3-COBCl{NtBu(SiMe3)}}2] (1) and [{(η5-C5H5)Ni}3{μ3-COBX(NR2)}μ3-CO] (2a: NR2 = NtBu(SiMe3), × = Cl; 2b: NR2 = N(SiMe3)2, × = Cl; 2c: NR2 = NMe2, × = BNMe2Cl) were obtained by reaction of the anionic complexes K2[{Fe(CO)3}3{μ3-CO}2] and K[{(η5-C5H5)Ni(CO)] with the corresponding chloroboranes Cl2BNR2 {NR2 = NtBu(SiMe3), N(SiMe3)2}, or 1,2-dichlorodiboranes(4) B2(NMe2)2Cl2, respectively. The products are formed by a nucleophilic attack of the CO oxygen atom at the boron centres with subsequent salt elimination. All compounds were characterized by IR and multinuclear NMR spectroscopy, and the structures of 1 and 2c in the solid state were determined by single-crystal X-ray diffraction studies.
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1271-1279 
    ISSN: 1434-1948
    Keywords: Chirality ; Dinuclear complexes ; Rhodium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dinuclear and polynuclear metal complexes with octahedral centers coordinated to di- or polydentate ligands are often obtained as complicated mixtures of various stereoisomers. Stereospecific synthesis of such species is therefore of high current interest. Chiral derivatives of pyridine can be used for this purpose. Dinuclear μ-chloro-bridged RhIII complexes with two didentate, cyclometalated thienylpyridine-type ligands at each metal center are formed stereoselectively when pinene groups are fused to the pyridine rings. The two octahedral RhIII centers have homochiral configurations, ΔΔ and ΛΛ. The heterochiral diastereomer ΔΛ is not observed. With (8R,10R)-2-(2′-thienyl)-4,5-pinenopyridine [Hth4,5-(R,R)ppy] the ΔΔ to ΛΛ ratio is 9:1 when the separation eluent contains NaCl. Modeling the ΛΛ and the ΔΛ isomers of the dinuclear species shows crowding of the pinene groups in both cases; however, the strain can be released by relatively small distortions only in the case of the ΛΛ isomer. NO3- cleaves the dichloro bridge, yielding the mononuclear species Δ[Rh(L2)2(NO3)] (2) in a completely stereoselective manner when NaCl is replaced by KNO3 in the eluent mixture. The molecular structure has been determined by X-ray structure analysis for both the ΔΔ and the mononuclear complex Δ[Rh(L2)2(NO3)] (2) in order to confirm the configuration at the metal center. 1H-NMR, 13C-NMR and CD spectra were measured and the latter shows that the CD activity is solely due to the chirality at the metal center.
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1281-1289 
    ISSN: 1434-1948
    Keywords: Phosphaalkynes ; Dimerization mechanism ; Diphosphacyclobutenes ; Density functional theory ; Ab initio calculations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dimerization of phosphaalkynes (R-C≡P, R = H, Me, tBu) without and with the presence of transition metal fragments, including CpCo (Cp = cyclopentadienyl) and COT-Ti (COT = cyclooctatetraene), has been probed using density functional theory calculations (B3LYP with different basis sets). MP2 and CCSD(T) calculations were also performed for the [H2C2P2] systems. In an attempt to address the exciting controversy and uncertainty about phosphaalkyne dimerization, a number of dimer formation mechanisms proposed in the literature have been examined. Some new and plausible intermediates have also been identified.
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  • 15
    Electronic Resource
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1315-1324 
    ISSN: 1434-1948
    Keywords: Ab initio calculations ; EHMO ; Vinylidene complexes ; Cobalt ; Rhodium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The transformation of acetylene into vinylidene, as promoted by the metal fragment [(pp3)Co]+ [pp3 = P(CH2CH2PPh2)3], is unimolecular and features the hydride-acetylide species as an intermediate. The paper describes a detailed ab initio study of the reaction, in particular with regard to the step involving 1,3-H shift. The best computational results are obtained by mimicking the pp3 ligand with actual ethylenic chains rather than with single PH3 molecules. The keypoints along the two-step reaction path (π-acetylene, hydride-acetylide, and vinylidene complexes, as well as intermediate transition states) have been optimized for CoI and RhI derivatives at the MP2 level. For the fragment [(pp3)Co]+, the barrier associated with transformation of the hydride-acetylide intermediate to vinylidene (20.6 kcal/mol) is easier to surmount compared to that for reversion to the reactants (28.6 kcal/mol). The situation is reversed for the analogous RhI system, with the initial π-acetylene adduct being slightly more stable. Although higher in energy, the hydride-acetylide species is the experimentally detected product of the reaction of acetylene with the fragment [(pp3)Rh]+. The salient chemical aspects of the 1,3-H shift are discussed in terms of perturbation theory arguments. Parallel EHMO calculations, which have provided a relatively good consistency with the ab initio results, allow the proposal of an orbital rationale for the mode of migration of the hydride ligand along the substantially linear Co-Cα-Cβ grouping.
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  • 16
    Electronic Resource
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1335-1342 
    ISSN: 1434-1948
    Keywords: Photolysis ; Alkynes ; Matrix isolation ; DFT ; Oxygenations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photolytically-induced reactions of chromyl chloride with acetylene and but-2-yne (dimethylacetylene) in low-temperature argon matrices yield end-on ketene and dimethylketene complexes of O=CrCl2, respectively. The product formation probably results from an electrophilic attack of a Cr=O linkage on the C≡C triple bonds, leading to radical-like transition states or intermediates, which subsequently rearrange through 1,2-H or 1,2-methyl shifts. Consequently, allene is attacked at its central carbon and the allyl radical thus generated undergoes subsequent ring-closure to give a cyclopropanone complex of O=CrCl2.
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  • 17
    ISSN: 1434-1948
    Keywords: Copper chelates ; EPR spectroscopy ; Electronic structure ; Schiff base ligands ; Structure elucidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of tetrahedrally distorted copper(II) complexes with thiolate and imine coordination were synthesized. Schiff bases derived from 4-benzoyl-3-methyl-1-phenyl-2-pyrazoline-5-thione and various diamines were used as tetradentate ligands to obtain tetrahedrally distorted metal chelates with [CuN2S2] complex units. Crystal structures of the complexes 1, 2, 5 and 6 and of ligand H25 have been determined by means of single-crystal X-ray structure analysis. The structure data show a strong influence of the diamine building blocks on the tetrahedral distortion of the copper(II) complexes. Results of Extended Hückel LCAO calculations correlate strongly with structural, electrochemical, UV/Vis- and EPR-spectroscopic features obtained experimentally. The calculations confirm for the whole complex series a strong delocalization of the frontier orbitals. The highest fully occupied molecular orbital shows a weak contribution, resulting from thiolate donor atoms, whereas the antibonding singly occupied molecular orbitals (SOMOs) are distributed between the copper(II) centre (ca. 35-40%) and the N2S2 donor set. The SOMO energy significantly lowers with increasing tetrahedral distortion of the coordination sphere. The influence of the tetrahedral distortion of copper(II) complexes on redox potentials, UV/Vis and EPR spectra is discussed.
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  • 18
    ISSN: 1434-1948
    Keywords: Half-sandwich complexes ; Molybdenum ; Optically active complexes ; Rhenium ; Tungsten ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of (η5-PinCp*)Re(CO)3 [PinCp* = tetramethyl(pinanyl)cyclopentadienyl] is described. Successive substitution of two CO ligands by NO+ and PPh3 generates a 1:1 diastereomeric mixture of chiral-at-metal [(SRe)/(RRe)-(PinCp*)Re(CO)(NO)(PPh3)]BF4. The diastereomers are converted with sodium methoxide into the derivative “esters” (SRe)/(RRe)-(PinCp*)Re(COOCH3)(NO)(PPh3), and then with (+)-(R)-(1-naphthylethyl)amine to the “amides” (SRe)/(RRe)-(PinCp*)Re(NO)(PPh3)[CONHCH(CH3)C10H7] [(SRe)/(RRe) = 1:1]. Fractional crystallisation separates the (SRe) isomer with an optical purity of 〉 98%. The latter compound has been characterized by X-ray structure analysis. By treating the (SRe)-amide with CF3CO2H and NaBF4, (SRe)-(PinCp*)Re(CH3)(NO)(PPh3) can be generated. Protolysis of this compound with HBF4/Et2O in CD2Cl2 at -78 °C leads to the solvent-stabilized complex (SRe)-[(PinCp*)Re(NO)(PPh3)(ClCD2Cl)]+BF4-. The thermal and configurational stability of this chiral Lewis acid is investigated at various temperatures. The syntheses of [PinCp*RhCl2]2, PinCp*TiCl3 and PinCp*M(CO)2(NO) (M = Mo, W) are also described. Starting with PinCp*M(CO)2(NO), the relatively stable 16-VE complexes PinCp*MCl2(NO) and PinCp*W(CH2SiMe3)2(NO) are synthesized.
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  • 19
    ISSN: 1434-1948
    Keywords: 2,2′-Bipyridines ; Chelate complexes ; Hydrogen bonding ; π-π stacking ; Crystal structure ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new synthetic route for the synthesis of 5,5′-diamino-2,2-bipyridine (5) based on the coupling of 2-chloro-5-aminopyridine in the presence of NiCl2 × 6 H2O/PPh3/Zn in dimethylformamide is described. The reactions of the potentially ambidentate ligand 5 with salts of the transition metals Mn, Fe, Ni, Cu, Zn, Ag, and Cd gave a variety of 13 metal-ligand complexes depending on the anion, the crystallization conditions and the metal-to-ligand ratio. The complexes obtained were characterized by thermal analyses, NMR including 113Cd-NMR, IR, and for the iron complex 57Fe-Mößbauer spectroscopy. The structure of eight of the compounds was elucidated by X-ray crystallography. All of these metal complexes show a bipyridine-metal coordination. The amino functionality was never involved in metal coordination. The intermolecular arrangement is dictated by hydrogen bonding from the amino functionality and by π-π stacking of the bipyridine rings.Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2005/1999/99078_s.pdf or from the author.
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  • 20
    ISSN: 1434-1948
    Keywords: Iron(III) ; Peroxo Complexes ; Kinetics ; Hydrogen Peroxide ; Catalase ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new diiron complex [Fe2(tbpo){O2As(CH3)2}(CH3O)(CH3OH)](ClO4)3 · 5 CH3OH · 2 H2O (1) containing a (μ-alkoxo)(μ-dimethylarsinato)diiron(III) core was synthesized using the heptadentate ligand N,N,N′,N′-Tetrakis(2-benzimidazolylmethyl)-1,3-diamino-2-propanol (Htbpo). The complex was characterized structurally by X-ray crystallography. 1reproduces the coordination mode and the stoichiometry of the proposed purple acid phosphatase-arsenate inhibitor complex. More importantly, 1 is a good functional model for the activation of small molecules, since the solvent molecule in the coordination sphere of each iron ion can be substituted very easily by a small substrate molecule. This is confirmed by the comparatively high pH-dependent catalase-like activity of 1. In order to study the influence of the cacodylate bridge on the formation of the metastable adduct with hydrogen peroxide, the analogous hydroxo-bridged complex [Fe2(tbpo)(OH)(NO3)2](NO3)2 · CH3OH · 2 H2O (2) was employed. The reactions of 1and 2 with H2O2 were studied as a function of [H2O2], pH, temperature, and pressure, and the kinetic results including the activation parameters are reported. In the case of compound 2 the reaction proceeds in one step, and the observed first order rate constant, kobs, shows a linear dependence on the hydrogen peroxide concentration with a zero intercept. For complex 1 the kinetic traces could be fitted to two exponential functions. One of the observed pseudo-first-order rate constants, kobs1, exhibits a linear dependence on the hydrogen peroxide concentration with a zero intercept, whereas the other rate constant, kobs2, was independent of the hydrogen peroxide concentration. A mechanistic interpretation is presented.Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2005/1999/99068_s.pdf or from the author.
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  • 21
    ISSN: 1434-1948
    Keywords: Ruthenium ; Coordination chemistry ; Paramagnetic complexes ; Magnetic properties ; Ion exchange ; Antitumor agents ; Colon tumors ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indazolium trans-tetrachlorobis(indazole)ruthenate(III) exhibits excellent results against different tumor models in vitro and in vivo. To improve the water solubility necessary for the introduction of this tumor-inhibiting compound into clinical trials, we synthesized the corresponding sodium salt in a two-step ion exchange via the tetramethylammonium salt. The sodium salt shows a 35-fold higher solubility in water relative to the indazolium salt. We also synthesized the n-butylammonium, n-octylammonium, and tetraphenylphosphonium salts, all of which showed improved solubility in organic solvents. The X-ray crystal structure of the latter could be solved, proving the trans configuration of the complex anion. In spite of the paramagnetic RuIII center an assignement of the coordinated indazole protons could be made with the help of a COSY experiment.
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  • 22
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2355-2368 
    ISSN: 1434-1948
    Keywords: Phosphane complexes ; Lithium ; Aminophosphanes ; Hydrazides ; (N-lithioamino)diorganophosphanes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Butyllithium (nBuLi) deprotonates Ph2P-NHtBu in ether to give (Ph2P-NLitBu)2·OEt2. There is no Li···P interaction in this molecule. Three compounds of the type R′P(NLiR)2 have been obtained by lithiation of R′P(NHR)2, isolated as [BuP(NLitBu)2·OEt2]2, [PhP(NLiPh)2·OEt2]2 and [PhP(NLiPh)2]2. Reaction of nBuLi with MeP(NHiPr)2 in hexane/THF leads to [MeP{N(Li)iPr]2·THF}4 with an asymmetric cluster structure comprising one LiP3, three LiPN2, three LiP2N and one LiN3 cluster units. The molecular structures of these compounds as determined by X-ray structure analysis show that they are best depicted as N-lithioaminophosphanes and not as the isomeric P-lithioiminophosphoranes.
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  • 23
    ISSN: 1434-1948
    Keywords: Alkylation ; Carbonyl complexes ; Lewis acids ; Phosphaalkenes ; Protonation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of the carbonyl-functionalized phosphaalkenes RC(O)P=C(NMe2)2 [R = tBu (2a), Ph (2b)] with protic acids and alkylating reagents occurred at the two-coordinate phosphorus atom to give the phosphanyl-substituted carbocations 3a,b and 4a,b. In contrast, treatment with Me3SiOSO2CF3 resulted in attack at the oxygen atom by the silyl group, and the formation of [RC(OSiMe3)=PC(NMe2)2]SO3CF3 (5a,b). Similarly, the Lewis acids B(C6F5)3, Al(tBu)2Cl and AlMe3 were ligated to the oxygen atom of the carbonyl group. Two equivalents of GaMe3 were added to the oxygen and phosphorus atom of the phosphaalkene to yield the thermolabile complexes [RC(OGaMe3)=P(GaMe3)C(NMe2)2] (10a,b). In contrast, one molecule of InMe3 was bound to the phosphorus center of the phosphorus compound. Reaction of the phosphaalkenes with [Ni(CO)4], [Fe2(CO)9] or [{(Z)-cyclooctene}Cr(CO)5] also took place at the pnictogen atom, resulting in complexes of the type [RC(O)P{M(CO)n}C(NMe2)2] (R = tBu, Ph; M = Ni, n = 3; Fe, n = 4; Cr, n = 5). The chemical transformations reported here underline the versatile chemistry of phosphaalkenes and emphasize a relationship between carbonyl-functionalized phosphaalkenes and the well-investigated class of phosphorus ylides. X-ray structures of compounds 6b, 7b*, 10a, 11a and 12a are reported.
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  • 24
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    AIChE Journal 42 (1996), S. 10-22 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Formation of asphalt aggregates and their deposition on the pore surfaces of a porous medium, which alter the structure of the medium and its effective properties, is a critical problem to catalytic and oil recovery and refinery processes. Extensive new experimental data for the amount of precipitated asphalt formed with crude oil and various solvents are presented. Results indicate that, contrary to the previous assumptions, asphalt formation is at best partially reversible. A thermodynamic model based on the Flory-Huggins theory of polymer solutions is used, together with the Soave equation of state, to predict the data. Critical evaluation of the model shows that its predictions do not agree well with our data. As an alternative, we propose a new model that employs a scaling equation, somewhat similar to those encountered in aggregation and gelation phenomena. The scaling function takes on a very simple form, and its predictions are in very good agreement with the data. It also predicts that the onset of precipitation may obey a simple universal equation.
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    AIChE Journal 42 (1996), S. 55-67 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The competition between drying and reactions in a liquid coating containing precursors to a random network polymer can give rise to a variety of drying phenomena. Solidification, or gelation, of the polymer may occur before, after, or during the removal of solvents from the coating. Rates of drying and reaction are probed by solving the equations of mass transfer by diffusion along with chemical reaction in one dimension. Solutions to this system of equations are obtained by Galerkin's method with finite-element basis functions and entail large-scale computation. Skinning, or solidification at the surface of the coating while the bulk is still liquid, occurs in thick coatings when the diffusional resistance to drying is significant, that is, at high mass-transfer coefficients. Homogeneous solidification occurs in thin coatings at low mass-transfer coefficients. Drying regime maps represent these solidification phenomena as regions in parameter space.
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    AIChE Journal 42 (1996), S. 96-130 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Recent and ongoing research in the distillation of nonideal mixtures is reviewed focusing on advances in the methodologies for the synthesis, design, analysis and control of separation sequences involving homogeneous and heterogeneous azeotropic towers. Maps of residue curves and distillation lines are examined, as well as geometric methods for the synthesis and design of separation sequences, trends in the steady-state and dynamic analysis of homogeneous and heterogeneous towers, the nonlinear behavior of these towers, and strategies for their control.Emphasis is placed on the methods of computing all of the azeotropes associated with a multicomponent mixture, on the features that distinguish azeotropic distillations from their zeotropic counterparts, on the potential for steady-state multiplicity, and on the existence of maximum and minimum reflux bounds. Important considerations in the selection of entrainers are examined. For the synthesis of separation trains, when determining the feasible product compositions, the graphical methods are clarified, especially the conditions under which distillation boundaries can be crossed and bounding strategies under finite reflux. The application of geometric theory to locate the fixed points, at minimum reflux, is reviewed in connection with homotopy-continuation algorithms for this purpose. The use of homotopy-continuation algorithms, especially for the steady-state simulation of heterogeneous azeotropic distillations, is justified. Methods for phase stability analysis are reviewed in connection with the location of real bifurcation points at phase transitions, an important feature of algorithms for the dynamic simulation of heterogeneous azeotropic distillations.
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    AIChE Journal 42 (1996), S. 187-203 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Discrete-time nonlinear feedback control laws are derived for multivariable nonlinear processes, whose “delay-free” parts are minimum phase. These include mixed error-and state-feedback, error-feedback, and mixed error- and output-feedback laws, which can induce linear input-output closed-loop response. This study is carried out within the framework of the discrete-time globally linearizing control. The broader class of nonlinear processes, in which controlled outputs as well as some other process variables are measured, are also considered. A mixed error- and output-feedback control law is derived for this class of processes. The conditions under which the mixed error- and output-feedback can be applied to a process operating at or around an open-loop unstable equilibrium point are determined. The application and performance of the derived control laws are illustrated by the numerical simulation of a chemical reactor.
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    AIChE Journal 42 (1996), S. 214-231 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The long-time behavior of a reaction mixture containing infinitely many species in isothermal continuous stirred tank reactors (CSTRs) is analyzed and contrasted with that in a plug-flow reactor (PFR). The reaction kinetics considered are irreversible first-order, irreversible coupled pseudo first-order, and reversible first-order. Asymptotic lumped kinetics for the mixture as a whole are developed as a function of feed properties and reactor type. Such lumped kinetics in many cases are of the power law form, with the exponent for a CSTR being lower than that for a PFR. Conditions under which non-power-law kinetics arise are given. Due to the wide spread of reactor residence times, the mixture in CSTRs admits a much richer variety of asymptotic possibilities than in the PFR. The results uncover some behavioral differences and relationships between CSTRs and a PFR for converting complex mixtures such as petroleum distillates or coal liquids.
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    AIChE Journal 42 (1996), S. 258-258 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996) 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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    AIChE Journal 42 (1996), S. 319-331 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A unified network model is formulated for predicting effective Fickian diffusivities of condensable vapors in porous media where capillary condensation and adsorption-desorption hysteresis occur. The model unifies the equilibrium theory based on the poreblocking interpretation of hysteresis in the interconnected network of pores and the percolation model of mass transport in the network with randomly interspersed regions for capillary condensation and surface flow. The Bethe network is used to represent the porous medium, and the effective medium theory is employed to obtain the effective diffusivity. Using the information on the connectivity and the positions of the closure points of the hysteresis loop enclosed by the equilibrium primary adsorption and primary desorption isotherms, the concentration dependence of the effective diffusivity is predicted. The model is applied to the systems water vapor-silica gel, water vapor-activated alumina, and literature data. It successfully predicts the concentration dependence of the effective diffusivity in the whole range of relative pressures for systems both with and without a peak in the diffusivity.
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    AIChE Journal 42 (1996), S. 359-368 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A model of simultaneous heat and mass transfer presented describes drying with internal heat generation. Since a liquid expulsion phase is observed, a numerical procedure was developed to account for saturated and unsaturated zones and to model the liquid expulsion. The model was validated by a drainage experiment. An experimental rig was built to conduct microwave drying experiments in well-controlled conditions using capillary porous body (light concrete) as test material. Two types of drying (high and low power) were distinguished, depending on whether or not boiling occurred in the sample. The heat source term in the medium was determined from the experimental results. The numerical results agree with the experimental observations in terms of drying kinetics and transfer mechanisms. This allows a very accurate description of the transport phenomena and the liquid expulsion phase associated with high-power drying.
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    AIChE Journal 42 (1996), S. 277-284 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 259-268 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A simple model was developed to describe the absorption of SO2 in a circulating dry scrubbing (CDS) process, which is a semidry, lime-based, flue-gas desulfurization (FGD) process that utilizes a circulating fluidized bed arrangement for contacting a sorbent with SO2-laden flue gas under “coolside” conditions. The reaction chemistry is thought to be similar to that of spray-drying absorption. The liquid-phase mass-transfer coefficient was successfully modeled as a function of the sorbent particle spacing on the wetted surfaces. Gas-phase mass-transfer resistances were assumed to be insignificant. Due to the high surface area available in a CDS reactor, the evaporation rate of water from the slurry was modeled as “constant-rate” drying according to classic spray-dryer theory. However, the “falling-rate” and “diffusion” evaporation stages were negligible in CDS since sorbent particle bunching at the surface of the slurry is nonexistent.
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    AIChE Journal 42 (1996), S. 271-276 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 298-300 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 332-346 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The flows generated in vessels stirred by two Rushton impellers were investigated in two vessels of diameter (T) 100 and 294 mm with impellers of diameter D = T/3 using flow visualization, power consumption, mixing time, and 360° ensemble-averaged and 1° angle-resolved LDA measurement techniques. The flows depended strongly on the clearance of the lower impeller above the base of the vessel (C1), the separation between the impellers (C2), and the submergence (C3) of the upper impeller below the top of the liquid column height (H). When these distances were varied, three stable and four unstable flow patterns were observed. Comparisons between the two LDA techniques showed that while the 360° ensemble-averaged measurements are useful for characterizing the overall flow structure and turbulence levels in the vessel, care must be exercised when interpreting such data, since in the impeller region they include periodic variations in the mean velocity in addition to the turbulent fluctuations. The trailing vortex structure and flow periodicity produced by the Rushton impellers is shown to decay significantly within a cylindrical region of height 1.2D and radius 1.0D centered around the middle of the vessel, when C1 = C2 = T/3. The turbulence structure within this region is anisotropic, while outside this region it might be considered mostly isotropic. The main flow features scaled well between the vessels.
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    AIChE Journal 42 (1996), S. 369-382 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A computer-aided simulator of steady-state two-phase flow in consolidated porous media is developed. The porous medium is modeled as a 3-D pore network of suitably shaped and randomly sized unit cells of the constricted-tube type. The problem of two-phase flow is solved using the network approach. The wetting phase saturation, the viscosity ratio, the capillary number, and the probability of coalescence between two colliding ganglia are changed systematically, whereas the geometrical and topological characteristics of the porous medium and wettability (dynamic contact angles) are kept constant. In the range of the parameter values investigated, the flow behavior observed is ganglion population dynamics (intrinsically unsteady, but giving a time-averaged steady state). The mean ganglion size and fraction of the nonwetting phase in the form of stranded ganglia are studied as functions of the main dimensionless parameters. Fractional flows and relative permeabilities are determined and correlated with flow phenomena at pore level. Effects of the wetting phase saturation, the viscosity ratio, the capillary number, and the coalescence factor on relative permeabilities are examined.
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    AIChE Journal 42 (1996), S. 431-439 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The crystallization of phenanthrene from toluene with carbon dioxide as the antisolvent gas is described. In the GAS process, a pressurized gas is dissolved into a liquid solvent, where it causes a volumetric expansion and lowers the solubility of the solute. Theoretical models are presented for the liquid-phase expansion and the solubility as a function of pressure and temperature. The Nývlt theory for batch crystallization is adapted to predict the pressure profile in the crystallizer needed to maintain a constant supersaturation and growth rate. Generation of seeds is accomplished via a pressure pulse at the saturation pressure. The average particle size of the phenanthrene could be varied from 160 to 540 μm. Creation of seeds doubles the particle size and reduces the coefficient of variation significantly. The residual amount of toluene in the crystals without treatment is approximately 70 ppm. The particles are agglomerates of phenanthrene crystals.
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    AIChE Journal 42 (1996), S. 440-454 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The high throughput and operating cost of the reactor provide the economic incentive in considering the on-line optimization of the LDPE tubular reactor. For an on-line optimization procedure it is crucial to develop a flexible and adaptive on-line parameter estimator, which based on the appropriate measurements from the reactor will adjust certain key model parameters so that the model can capture the actual reactor operation and reliably be used for the real-time optimization of the reactor performance. Various issues involved in developing the on-line estimator for such applications as the mathematical modeling of the reactor, the selection of the adjustable model parameters and reactor measurements, the decomposition of the problem according to the characteristic time constants of various disturbances, and the efficient and robust solution of the mathematical problem are discussed. The tools developed were successfully used on an EXXON high-pressure LDPE tubular reactor. Results from the numerical experiments that are compared with scaled data from a real reactor show that the estimated temperature profiles agree remarkably with those observed at various phases of the reactor operation.
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    AIChE Journal 42 (1996), S. 595-598 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 601-612 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A previously developed mathematical wetting model is generalized and applied to the following two closely related situations: the spreading of a liquid over a prewet solid surface and the receding contact-line motion with a microscopic residual film, remaining behind the contact line. An analytical expression for the velocity dependence of the dynamic contact angle is derived. Macroscopic characteristics (the dynamic contact angle and drag force) and the flow field corresponding to the spreading of a liquid over a wet solid surface differ considerably from those calculated for a dry surface. Under certain conditions the flow in the reference frame fixed with respect to the contact line has a region with closed streamlines. The region appears due to the flow-induced Marangoni effect, the reverse influence of the surface tension gradient along the liquid-solid interface caused by the flow on the flow, which gives rise to the gradient. The results are compared qualitatively with experimental data.
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    AIChE Journal 42 (1996), S. 683-690 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Simulated countercurrent chromatography is a continuous flow method for separation of binary mixtures or for separation of multicomponent mixtures into two fractions. Countercurrent flow is simulated by moving the feed point past several fixed adsorbent beds at a rate between the single column breakthrough time of each component. The number of columns and the location of the inlet and outlet port were varied to investigate product purity and productivity. Concentration profiles of the effluent product streams were measured. The maximum product concentration exceeds the feed concentration during part of the feed-switching cycle and drops to zero during part of the cycle. Three configurations were tested with the total number of columns varying between three and eight. For the test separation chosen, gaseous propylene and dimethyl ether on Chromosorb 101, high purity (〉 99%) product streams were obtained with an optimal four-column configuration using three desorbent streams.
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    AIChE Journal 42 (1996), S. 700-712 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The frequency response method measuring the temperature and pressure of an adsorbent sample determines the mass- and heat-transfer kinetics in adsorbents, especially in zeolites. The temperature of the sample (large crystals or monolayers of pellets) is measured by infrared detection. The main aspects of the in-phase and out-of-phase functions as given by an analytical bidispersed model are described. They depend on characteristic times related to kinetic paprameters. Experimental results on adsorption of water on NaX zeolite (crystals or pellets) show that this method allows heat transfer to be very clearly delineated from mass-transfer modes and the separation of different mass-transfer modes. For a bidispersed sample, macro- and microporous mass-transfer parameters may be obtained with the same sample. Results on a contaminated 5A zeolite-propane system show the presence of mass-transfer resistance at the pellet surface. The infrared temperature measurement associated with the frequency response appears to be powerful in determining kinetic adsorption, and gives more information than the pressure measurement.
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  • 45
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    AIChE Journal 42 (1996), S. 742-752 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: With the growing environmental concern, it is necessary to improve process simulation and develop design tools to account for environmental factors in the synthesis of large-scale chemical processes. A major obstacle in tackling this problem is uncertainties in some of the technical and economic parameters, which lead to uncertainties in design, plant performance, and cost estimates. Further, a conceptual process design involves the identification of an optimal flowsheet structure from many alternatives stituting the “superstructure.” Synthesis and optimization of large-scale processes involving uncertainties often require considerable computational effort. A novel algorithm presented here is based on simulated annealing for the process synthesis of large-scale flowsheets having several configurations and considers uncertainties in the process design systematically. This new “stochastic annealing algorithm,” provides an efficient approach to stochastic synthesis problems by incorporating a penalty term in the objective function and balances the trade-off between accuracy and efficiency based on the annealing temperature. It has been used to study a benchmark synthesis problem in the HDA process. Savings of up to 80% in CPU time has been achieved without significant loss of solution precision with stochastic annealing, compared to simulated annealing with a fixed sample size. It can be applied to analyze efficiently any complex process flowsheet and provide valuable insights into process feasibility based on optimal design, plant performance, and uncertainty issues.
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  • 46
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    AIChE Journal 42 (1996), S. 777-790 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Most advanced control applications rely on good dynamic process models. The performance of the control system depends on the accuracy of the model used. Typically, such models are developed by conducting off-line identification experiments on the process. These identification experiments often result in input-output data with small output signal-to-noise ratio, and using these data results in inaccurate model parameter estimates. Prefilters are used to separate useful information from the noise in the input-output data and to improve parameter estimates. A systematic design procedure for selecting a prefilter using discrete wavelet transforms is presented. The design procedure provides explicit information on the compromises in prefilter design, interpreted in terms of parameter variance and bias. The prefilter design procedure is then applied to identify a second-order output error model.
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  • 47
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    AIChE Journal 42 (1996), S. 820-828 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The new application of nuclear magnetic resonance imaging (MRI) techniques for characterizing fractures and flow in fractured media is investigated. Specifically, a relaxation-weighted imaging technique is used for selectively highlighting either fracture or porous matrix regions. Many advantages over conventional spin-density MRI techniques for characterizing fractured media are demonstrated. Its use to speed image acquisition is also demonstrated. In addition, a multislice profile imaging technique is used to investigate imbibition and drainage displacement experiments in fractured porous media. These images demonstrate that the fractures can have profound effects on the fluid distributions in multiphase flow.
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  • 48
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    AIChE Journal 42 (1996), S. 861-875 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A primary constituent in high-temperature (120-140°C) milk fouling residues is calcium phosphate in the form of calcium phosphate dihydrate (brushite, CaHPO4 · 2H2O) and hydroxyapatite [Ca5(PO4)3OH]. The removal of these mineral-rich deposits from stainless steel occurs by dissolution and mechanical cleaning. This research uses a novel solid scintillation technique to noninvasively and continuously investigate the removal of P32-labeled mixtures of calcium phosphate from inner surface of stainless steel tubes. The proposed mass-transfer model suggests that the film is initialy removed by dissolution, when compared to the experimental results. An alternative first-order model presented includes the effects of the solvent flow rate and solvent pH on decontamination rates. This model agrees with the experimental cleaning data over the range of pH and flow rates studied.
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    AIChE Journal 42 (1996), S. 884-888 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 896-900 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996) 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
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    AIChE Journal 42 (1996), S. 927-931 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The sedimentation velocity of multiparticle suspensions was investigated experimentally for cases where the column wall is likely to have a nonnegligible effect. The experiments demonstrate that the container wall diameter influeces the falling velocity only for dilute systems, which is in contrast with a widely used, established empirical relationship.
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    AIChE Journal 42 (1996), S. 953-959 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The formation of a filter cake during mechanical dewatering (filtration and expression) of sludge is studied using one-dimensional nuclear magnetic resonance (NMR) imaging of porosity profiles. The experiments clearly showed the formation of a porosity gradient during filtration and the disappearing of this gradient during expression, forming a cake with a uniform porosity. This technique makes it possible to investigate the material behavior of the porous medium, which is needed before any model calculations can be performed. The results indicate that NMR imaging is useful in nondestructive monitoring of the filtration and expression process of sludge.
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    AIChE Journal 42 (1996), S. 973-982 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A model that makes it possible to evaluate the secondary nucleation rate in a pilot-scale industrial crystallizer is presented. It relates the secondary nucleation rate directly to the volume rate of attrition of large parent crystals. Two other terms are included in the equality, one that expresses the distribution formed by the attrition fragments, and the other that expresses a survival efficiency accounting for the percentage of attrition fragments that grow out after the attrition step. The model is further tested on a 970-L draft-tube-baffled evaporative crystallizer with ammonium sulfate as the model material used for crystallization and having an on-line crystal size-distribution measuring device.
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    AIChE Journal 42 (1996), S. 1010-1032 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A generalized modeling framework for process synthesis alternatives is proposed, based on fundamental mass/heat-transfer principles. A multipurpose mass/heat-transfer module is introduced as the building block of the framework, whereas basic block-superstructure rules (such as splitting, mixing, and bypassing) are used to develop a systematic representation of process units and process structures, conventional or not. Process synthesis procedures are explored within this modeling framework, where synthesis alternatives are not postulated as process unit networks, but explored simultaneously without predefining synthesis schemes, as combinations of mass/heat-exchange stream matches. The representation potential of this framework is illustrated with examples from unit operations, whereas synthesis example problems are presented to show the broad range of process alternatives that can be modeled, identified, and optimized.
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    AIChE Journal 42 (1996), S. 1041-1068 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The study of spatial structures in heterogeneous reactors is a challenging academic topic, revealing patterns that differ from those known to exist in reaction-diffusion systems exposed to uniform conditions, as well as a practical problem that should affect design and operation procedures of commercial reactors like the catalytic convertor. Experimental observations and mathematical models of spatiotemporal patterns in high-pressure catalytic reactors are reviewed. Patterns in high-pressure reactors, in which thermal effects provide the positive feedback, as well as the long-range communication, usually emerge due to global interaction. Patterns are classified comprehensively by considering reactors of increasing degree of complexity: a wire or ribbon exposed to uniform conditions, a globally coupled catalyst in a mixed reactor or in a control loop, and a fixed bed in which interaction by convection occurs only in one direction. Catalytic wires are not expected to exhibit sustained patterns in the absence of global interaction. Global interactions by external control or gas-phase coupling are shown experimentally and analytically to induce a rich plethora of patterns. Complex motions were simulated to occur due to the interaction of convection, conduction and reaction in a fixed-bed; only a few of these patterns were experimentally observed. Directions for future research are suggested.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2127-2134 
    ISSN: 1434-1948
    Keywords: Gallium ; Azides ; Chemical vapour deposition ; Gallium nitride ; Single source precursors ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis, properties and X-ray single crystal structure analysis of the intramolecularly adduct-stabilised organogallium bisazide (N3)2Ga[(CH2)3NMe2] (1), the mono azide (N3)Ga[(CH2)3NMe2]2 (2) and the trialkylamine adducts of triazidogallium of the type (N3)3Ga(NR3) (3a-d; R = alkyl) are reported. An unusual isomer 1b of compound 1 is described, which was obtained by slow cooling of the analytically pure neat liquid compound 1 to 0 °C. The new and unusual structure 1b can be regarded as a weak associate of dimers linked together by head-to-tail azide bridges. In contrast, compounds 2 and 3a-b (R = CH3, C2H5) are monomeric in the solid state. The suitability of the volatile compounds 1 and 2 as single source precursors to grow GaN thin films by chemical vapour deposition is compared, showing that preferentially oriented crystalline films can be obtained from compound 2 on sapphire substrates at 600-700 °C in vacuo (0.1 Pa). However the films have a grey rather than a transparent appearance, which is presumably due to N-deficiency owing to the lower N-content of the single molecule precursor 2 relative to 1.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2135-2145 
    ISSN: 1434-1948
    Keywords: Density functional calculations ; Epoxidation ; Peroxo complexes ; Titanium ; Transition states ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Epoxidation of olefins by TiIV peroxo and hydroperoxo (alkylperoxo) complexes was investigated using a hybrid DFT method (B3LYP). Reaction energies and activation barriers for direct oxygen transfer to ethylene as a model olefin were computed for various model complexes to compare the epoxidation activity of Ti(η2-O2) and TiOOR (R = H, CH3) moieties. The activity of complexes with a Ti(O2) peroxo group is shown to be essentially quenched when the coordination sphere of the complex is saturated by strongly basic (σ-donor) ligands. In contrast, the activity of a TiOOH functional group depends only weakly on the saturation of the coordination sphere of the Ti center. Substitution of methyl for hydrogen in a TiOOH group is found to slightly increase the activation barrier of epoxidation. The computational results give preference to reaction paths that involve TiOOR species. The factors governing the activity of Ti(O2) and TiOOR groups, in particular the effects of donor ligands, are discussed on the basis of a molecular orbital analysis.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2289-2294 
    ISSN: 1434-1948
    Keywords: Intercalations ; Vanadyl phosphate ; Ethanol ; Hydration ; Kinetics ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The course of the replacement of ethanol by water molecules in the VOPO4·2C2H5OH intercalate, and of water by ethanol in VOPO4·2H2O has been studied by X-ray diffraction and infrared and Raman spectroscopy. Formation of mixed phase VOPO4·C2H5OH·H2O was not observed. The shape of the kinetics curves indicates a transition of at least one reaction zone through the crystal. A delay in formation of the product in comparison with the decrease in the amount of starting material can be explained by the existence of non-diffracting advancing phase boundary. In a VOPO4/ethanol/water system, VOPO4·2C2H5OH is formed as the only product when the system contained more than 96 vol% of ethanol, whereas in the system with less than 94 vol% of ethanol only VOPO4·2H2O is present.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 2295-2299 
    ISSN: 1434-1948
    Keywords: Lewis acids ; Bismuth ; Aluminum ; Phosphorus ; Tin ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dilithium salts of N-methyl-N′,N′′-bis(diisopropyl)- and -(trimethylsilyl)-diethylenetriamine 1a,b react with SnCl2 affording the corresponding stannylenes 2a,b in 60 and 80% yield, respectively. Compound 1b also reacts with BiCl3 to give the bismuth chloride 5 (90% yield). Derivatives 2b and 5 have a symmetrical bicyclic structure and are monomeric both in solution and in the solid state. When 2b is treated with BiCl3 or PCl3, an oxidation reaction leads to the hypercoordinated tin(IV) dichloride 3 (58% yield), or a transmetallation gives rise to the oniophosphane 4 (95% yield), respectively. Transmetalation reactions also occurred when 5 was treated with AlCl3, GaCl3 or SnCl2 affording the corresponding aluminum chloride 6 (81% yield), gallium chloride 7 (38% yield) or tin dichloride 3 (38% yield). The observed reactivity for 2 and 5 is compared to that reported for Veith's stannylene or bismuth chloride.
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  • 61
    ISSN: 1434-1948
    Keywords: Ruthenium ; Triazole ; Titanium ; Electron Transfer ; Sensitizers ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexes [Ru(dcb)2(L)] {L = 3-(2-hydroxyphenyl)-5-(pyridin-2-yl)-1,2,4-triazole (2-ppt), 3-(4-hydroxyphenyl)-5-(pyridin-2-yl)-1,2,4-triazole (4-ppt), 3,5-bis(pyrazin-2-yl)-1,2,4-triazole (bpzt), 3-(2-hydroxyphenyl)-5-(pyrazin-2-yl)-1,2,4-triazole (2-ppzt) and dcb = 4,4′-(CO2H)2-2,2′-bipyridine} have been synthesized, spectroscopically characterized and anchored to nanocrystalline TiO2 electrodes for the conversion of light into electricity in regenerative solar cells. The different efficiencies observed have been rationalized on the basis of an analytical expression relating the incident photon-to-current conversion efficiency (IPCE) to the kinetic parameters of the relevant electron transfer processes involved in the solar cell.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1295-1299 
    ISSN: 1434-1948
    Keywords: Solid-state chemistry ; Structure elucidation ; Reactive flux syntheses ; Oxysulfides ; Niobium chalcogenides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new compounds K4Nb2S10O and Rb4Nb2S10O have been synthesized by the reaction of potassium or rubidium alkaline polychalcogenides with NbO2, Nb2O5, or mixtures of Nb and NbO. Their structures consist of discrete [Nb2Q11]4- anions (Q = O, S) built up of two face-sharing pentagonal bipyramids, which are connected via the alkali metal cations.
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    ISSN: 1434-1948
    Keywords: Pyrazolato ligands ; Rhenium ; Group-11 metals ; Heterometallic complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By treating [(CO)3Re(Hpz)2(pz)] (Hpz = pyrazole) with [Cu(CH3CN)4]BF4, AgNO3, or [Au(tht)Cl] (tht = tetrahydrothiophene) in acetonitrile in the presence of Et3N, the corresponding trinuclear complexes {(CO)3Re(pz)3[M(CH3CN)]2} (1a-c) have been obtained. Treatment of complexes 1a-c with cyclohexyl isocyanide (c-C6H11NC) afforded the derivatives {(CO)3Re(pz)3[M(c-C6H11NC)]2} (2a-c). Complexes 2a-c have been characterized in solution by 1H-NMR spectroscopy and in the solid state by single-crystal X-ray diffraction analysis.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1309-1313 
    ISSN: 1434-1948
    Keywords: Phthalocyanines ; Rhenium ; Nitrido(octa-n-alkylphthalocyaninato)rhenium compounds ; Nucleophilic additions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of nitrido(tetra-tert-butylphthalocyaninato)rhenium (1) with boron tribromide leading to (tBu4Pc)ReNBBr3 (4) and with acetone to give the imido complex (tBu4Pc)Re[NC(CH3)2CH2C(O)CH3]OH (2b) and its μ-oxo dimer 3 are reported. Starting from the corresponding 4,5-di-n-alkylphthalonitriles and ammonium perrhenate four soluble nitrido(octa-n-alkylphthalocyaninato)rhenium complexes 5-8 were synthesized. Nitrido(octa-n-pentylphthalocyaninato)rhenium (6) was treated with boron tribromide to afford [(C5H11)8Pc]ReNBBr3 (9).
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1325-1333 
    ISSN: 1434-1948
    Keywords: Platinum ; Palladium ; Platinum blues ; Naphthyridine complexes ; Trinuclear complexes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: All three dinuclear complexes [Pd2(donp)2(bpy)2] (1) (H2donp = 1,8-naphthyridin-2,7-dione), [Pd2(H2nonp)2(bpy)2](ClO4)2 (2), and [Pt2(H2nonp)2(bpy)2](PF6)2 (3) (H3nonp = 7-amino-1,8-naphthyridin-2-one) exhibit the μ-1ĸN1:2ĸN8 bridging mode for their head/tail orientated naphthyridine ligands. Whereas 1 and 3 may be prepared by direct reaction of the dinucleating ligand with [MCl2(bpy)], formation of competing tripalladium(II) complexes must be avoided for 2 by employment of the precursor H2acnonp (7-acetamido-1,8-naphthyridin-2-one), which affords [H2nonp]- on cleavage of its original acetyl group. A mixture of the head/tail (4a) and head/head (4b) isomers of [Pd3(Hnonp)2(bpy)3](ClO4)2 is obtained when H3nonp is treated with [PdCl2(bpy)] and LiOH at room temperature for 2 d, followed by precipitation with LiClO4. Contrastingly exclusive formation of 4a is observed upon refluxing this reaction mixture for 3 d in aqueous solution. The [Hnonp]2- ligands exhibit a μ3-1ĸN1:2ĸN8:3ĸN7 bridging mode that leads to short Pd···Pd interactions of 2.781(2) and 2.775(2) Å. Similar metal-metal distances of 2.771(3) and 2.816(3) Å are observed in head/head-[Pt3(acnonp)(Hnonp)(bpy)3]Cl2 (5). An in situ 2e--oxidation (Ag+/Ag) of the [Pt3]6+ core in triplatinum(II) species such as 5 formed by the reaction of [PtCl2(bpy)] with H2acnonp allows the isolation of diamagnetic dark-brown head/head-[Pt3(Hnonp)2(NO3)(bpy)3](ClO4)2(NO3) (6) with an average oxidation state of Pt (2.67+). The Pt-Pt distances of 2.723(2) and 2.670(2) Å are markedly shorter than in 5.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1343-1350 
    ISSN: 1434-1948
    Keywords: Indium ; O ligands ; N ligands ; C ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New heteroleptic indium compounds have been synthesized starting from indium(III) halides and hexamethyldisilazyllithium to form MeXInN(SiMe3)2 [X = Cl (1), Br (2)], and then subsequent alcoholysis to afford the molecules [ClMeIn(OtBu)]2 (3), [BrMeIn(OtBu)]2 (4), {ClMeIn[O(C6H4)OMe]}2 (5), {[(SiMe3)2N]MeIn(OtBu)}2 (6) and [MeIn(OtBu)2]2 (7). The molecular structures of molecules 3-7 have been obtained by single crystal X-ray diffraction studies. The structures of the compounds 3-7 are almost identical: 3-5 crystallize in the monoclinic crystal system with two dimeric molecules per unit cell in the space group P21/c, 6 crystallizes in the monoclinic space group C2/c with four molecules per unit cell, and compound 7 crystallizes in the triclinic crystal system with one dimeric molecule per unit cell in the space group P-1. The central centrosymmetric In2O2 ring, common to all the compounds, is achieved by two bridging oxygen atoms. Due to the additional coordination by an oxygen atom of the methoxy group, the coordination number of the metal center rises from 4 to “4+1” if the OtBu ligand (compounds 3, 4, 6, and 7) is exchanged for a methoxyphenol ligand (compound 5). In addition to the In2O2 ring the compound 5 possesses two annealed five-membered InO2C2 rings. The common indium methyl group of all compounds, which is transfered by an original route from the silicon to the indium atom, is used to compare structural and spectroscopic properties of the molecules, as there is a correlation between the In-C bond length and the chemical shift of the methyl group which depends on the ligand system used.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1359-1366 
    ISSN: 1434-1948
    Keywords: Selenium ; Fluorine ; Multinuclear NMR ; Raman spectroscopy ; X-ray crystallography ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of perfluoroaryllithium RC6F4Li, where R = F or 4-CF3C6F4O, respectively, with selenium gives the known diselanes (RC6F4Se)2 (1a, 1b). Redox reactions of 1 with hydrogen peroxide result in the formation of the seleninic acids RC6F4SeOOH which crystallize as hydrates (2a, 2b); with mercury give the bis(arylseleno)mercuries (RC6F4Se)2Hg (3a, 3b); with sulfuryl chloride or bromine give the selenenyl chlorides (4a, 4b) or selenenyl bromides (5a, 5b). Selenenyl chlorides (4a, 4b) react with a variety of trimethylsilyl reagents Me3SiX (X = Br, CN, NMe2, NEt2) to form 5a, 5b; selenocyanates RC6F4SeCN (6a, 6b); selenenyl amides RC6F4SeNMe2 (7a, 7b) and RC6F4SeNEt2 (8a, 8b). A new synthetic route to diorgano selanes is developed by reaction of 4a, 4b with perfluoroaryllithium to give the symmetric (RC6F4)2Se (9a, 9b). All derivatives are thoroughly characterized and in addition the molecular structures of 2a, 6a, and 9a are established by X-ray crystallography.
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  • 68
    ISSN: 1434-1948
    Keywords: Metallomesogens ; Nickel ; Salicylidenediamines ; Azo compounds ; (E)/(Z) photoisomerization ; Isomerizations ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bis[4-(n-CmH2m+1O)-5-(p-C14H29C6H4N=N)]-substituted N,N′-salicylidenediamines H2[LN(m,14)] (N = 1: 1,2-diaminoethane; N = 2: 1,3-diaminopropane; N = 3: 1,3-diamino-2,2-dimethylpropane; m = 6 or 18) have been synthesized. Both the N = 2 and 3 series of compounds display a smectic C (SmC) mesophase, with clearing points well below 100 °C. By treating the H2[LN(m,14)] ligands with an NiII salt, liquid crystalline mononuclear complexes with “unconventional” (lateral-tailed) molecular shape form. These Ni[LN(m,14)] complexes, showing nematic and smectic disordered phases, are stable over a quite large temperature range and have been characterized by different spectroscopic techniques. The newly synthesized mesogens exhibit lower transition temperatures and higher thermal stability than homologous complexes Ni[LN(14)] with a “conventional” rod-like molecular geometry.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1467-1477 
    ISSN: 1434-1948
    Keywords: Oxidations ; Tertiary alcohol ; Porphyrins ; Neophyl rearrangement ; Cleavage reactions ; β-Scission ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation of 4-(1-hydroxy-1-phenylethyl)benzoic acid HPEBA with a water-soluble metalloporphyrin as catalyst and KHSO5 as oxygen atom donor gives the major products, acetophenone AC and acetylbenzoic acid ABA, by a Caliph-CAr bond cleavage, but a minor product, benzoyloxybenzoic acid BOBA, requires the insertion of an oxygen atom to form the ester. This compound becomes the main oxidation product on increasing the amount of acetonitrile in the reaction medium, and its formation is oxygen-dependent. The conversion is drastically lowered by using D2O instead of H2O, suggesting that an alkoxyl radical is formed in the rate-determining step. Labeling experiments using 18O2 or H218O under different reaction conditions show that the carbonyl oxygen atoms of AC and ABA originate either from substrate, water or dioxygen. However, the carbonyl oxygen atom in the ester group of BOBA originates from dioxygen while the other oxygen atom of the ester remains unlabeled. These results can be explained by an O-neophyl rearrangement of the initial alkoxyl radical to afford a carbon-based radical which then reacts with dioxygen or MnIV-OH/water. In a competitive reaction pathway, direct β-scission of the alkoxyl radical leads to unlabeled products. The oxidation of other tertiary diaryl alcohols is also discussed.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1489-1495 
    ISSN: 1434-1948
    Keywords: Peroxo complexes ; Vanadium ; Mass spectrometry ; 51V-NMR spectroscopy ; Vanadium dependent bromoperoxidases ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ESI mass spectrometry and 51V-NMR spectroscopy have been used to study the reactions occurring between bisperoxo vanadates and a number of histidine and histidine-like ligands, in aqueous alcoholic solutions. Coordination of one and two molecules of ligand is observed with all the compounds investigated affording [VO5L]- and [VO52L]-, respectively. Characterization of these species has been achieved by MSn experiments, which have allowed specific fragmentations of the peroxidic moiety to be distinguished. In particular, with [VO52L]-, two distinct modes of decomposition were observed, depending on the presence in the ligand of a free carboxylic function. - Possible biochemical implications related to vanadium haloperoxidase enzymes are discussed.
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    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1479-1488 
    ISSN: 1434-1948
    Keywords: Phosphorus heterocycles ; Cations ; Tungsten complexes ; Coordination modes ; Phosphaalkenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1,1,3-tris(diisopropylamino)diphosphirenium salt 1 reacts with lithium aluminium hydride leading to the P-hydrogeno-C-phosphinophosphaalkenes 2, which on treatment with a catalytic amount of BF3·OEt2 afford the 1,3-bis(diisopropylamino)-1H-diphosphirene 3. The corresponding η1-coordinated 1H-diphosphirene 6 can be prepared by treatment of 2 or 3 with one equivalent of [W(CO)5(thf)]. Alternatively, the diphosphirenium salt 1 reacts with an excess of [W(CO)5(thf)], affording the corresponding η1-coordinated diphosphirenium salt complex 4, which is converted into the P-hydrogenophosphaalkene complex 5 with lithium aluminium hydride. The dinuclear tungsten complexes 7 and 8 are obtained by treatment of the free 1H-diphosphirene 3 with two equivalents of [W(CO)5(thf)] or one equivalent of [W(CO)4(thf)2], respectively. Compound 6 reacts with two equivalents of hydrogen chloride, giving the 1-chloro-3-diisopropylamino-1H-diphosphirene 9, which can be subsequently converted into the 1-diisopropylamino-, 1-azido, or 1-phenyl-3-diisopropylamino-1H-diphosphirenes 6, 10 and 11 by nucleophilic substitution with diisopropylamine, azidotrimethylsilane or sodium tetraphenylborate, respectively. The [η2-(3-diisopropylaminodiphosphirenylium salt)·W(CO)5] complexes 12a-c can be prepared by reaction of 9 with silver trifluoromethanesulfonate, aluminium or gallium trichloride or, alternatively, by treatment of 6 with two equivalents of trifluoromethanesulfonic acid. Reaction of 12a with diisopropylamine, water, bis(triphenylphosphoranylidene)ammonium chloride or tetrabutylammonium fluoride gives the corresponding 1H-diphosphirene complexes 6, 13, 9, or 14, respectively. Compound 12a also reacts with one or two equivalents of [W(CO)5(thf)], leading to the di- and tri-nuclear complexes 15and 16, respectively.
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    AIChE Journal 42 (1996) 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 2-9 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Diffusion of carbon dioxide through silicone-polycarbonate membranes containing oriented mica flakes is proportional to the square of the volume fraction of the flakes, to the square of the aspect ratio, and to the square of the cosine of the angle at which the flakes are oriented. These experiments are consistent with Monte Carlo simulations. The simulations allow investigation of more complex geometries, including other flake orientations and polydisperse flake sizes.
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    AIChE Journal 42 (1996), S. 42-54 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A laser-Doppler velocimetry (LDV) apparatus and a computational fluid dynamic (CFD) software package (FLUENT) were used to experimentally determine and numerically predict the velocities in a baffled vessel agitated by one or two 45° pitched-blade turbines. The flow characteristics in the impeller regions were measured by LDV and used as boundary conditions in the numerical computations. Turbulence effects were simulated using either the k-ε model or algebraic stress model (ASM). The CFD predictions were compared to the LDV measurements in terms of average velocities in all three directions as well as turbulent kinetic energies. Predictions based on ASM were typically in closer agreement with the experimental data than those based on the k-ε model. Flow patterns in both configurations were dominated by the axial and tangential components. The presence of the upper impeller altered the flow considerably, producing a strong vertical recirculation pattern between the impellers and significantly reducing the circulation flow below the lower impeller.
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    AIChE Journal 42 (1996), S. 87-95 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Liquid-solid fluidization characteristics of irregularly shaped Biobone particles were studied in a fluidized bioreactor column 2.35 m high and 0.1 m dia. The wet biobone particles had a density of 1,890 kg/m3. Two size ranges were studied: 1.70-2.36 mm and 1.25-2.36 mm. The Biobone is a natural cheap material composed of collagen, which is a strong protein structure, embedded with microcrystals of hydroxyapatite and calcium phosphate, and it is an excellent matrix of commercial importance used for the immobilization of enzymes, whole cells and other biocatalysts. Fluidization characteristics of Biobone particles, which include measurements of pressure drops, holdups, minimum fluidization velocities, particle entrainment, and residence time distributions at different water superficial velocities, are reported. Because of the highly irregular shape of Biobone particles, new fluidization behavior was observed, which was much different from the fluidization behavior of spherical particles reported in the literature. A new channeling index, Ic, is proposed to quantify the channeling characteristics of fluidized Biobone particles, and a new parameter, α, was developed to distinguish the transition between fixed and fluidized states of the Biobone particles.
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    AIChE Journal 42 (1996), S. 147-153 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: L-Isoleucine and the isomorphic amino acids L-leucine and L-valine serve as a model system in the examination of the effects of impurities on the purity and morphology of crystals recovered from batch crystallizations. Factors are determined that influence crystal purity and, concomitantly, crystal size and shape. Characteristics of the L-isoleucine crystal are determined by X-ray analysis and compare favorably with the literature. These and literature characteristics of L-leucine and L-valine are used in simulations to evaluate possible mechanisms by which lattice substitutions with impurities lead to size and morphological changes.
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    AIChE Journal 42 (1996), S. 154-160 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This article is intended as a complement to a recent article in this journal, “Comparative Study of Flow Schemes for a Simulated Countercurrent Adsorption Separation Process” by Ching et al. (1992). These authors carried out experiments on continuous separation of three carbohydrate mixtures with both the usual four-section scheme and a three-section scheme: fructose dextran (MW ≌ 9,400), raffinose dextran (MW = 6,000), and fructose-raffinose. These two schemes were modeled as equivalent true countercurrent systems. From the experiments and model results they conclude that the equivalent true countercurrent model is fully adapted to represent the four-section scheme, but a major discrepancy arises with the three-section scheme: the raffinate concentration is not correctly predicted.From these results it may be concluded that when a physically meaningful modeling of the equivalent true countercurrent is realized, the apparent discrepancy disappears. From another standpoint, such a mismatch between the experiments and model predictions would not have been observed with a model that considers the periodic port motion. Such a model foresees a cyclic steady state where extract and raffinate compositions vary throughout the period T; they can be considered as constant only when averaged over the period. It is worth comparing the results of these two models, especially when the equivalent countercurrent representation is not very close to the physical phenomenon it should represent.We agree with their major finding that a three-zone scheme represents necessarily a higher desorbent demand than a four-zone scheme.
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    AIChE Journal 42 (1996), S. 176-186 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A stable adaptive control strategy is suggested for a class of continuous-flow bioreactor processes described by Monod kinetics with two unknown parameters, one of which appears nonlinearly. Similarly, as in the case of the previously reported adaptive controllers, the parametrization of the process model, in conjuction with the adaptive exponential feeding strategy and corresponding adaptive algorithms, results in a stable system in which the convergence of the output errors to zero is guaranteed. In the former, however, two major problems are encountered: (1) both output errors were used to adjust the controller parameters, which may yield unacceptable performance of the resulting adaptive system; (2) conditions under which the process output can assume only positive values are difficult to derive. Hence, a design of a stable adaptive controller is suggested, whose parameters are adjusted using only one of the output errors and that yields acceptable performance of the control system. With this method, conditions under which the process outputs can assume only positive values can be readily derived. These conditions in turn guarantee that the control input saturation at value zero cannot occur. In this context, two adaptive controllers are suggested, such that the resulting adaptive systems are stable and the control objective is met. The adaptive controller design relies on a convenient coordinate transformation, while the proof of stability is based on suitably chosen Lyapunov functions. The performance of the adaptive system is evaluated through computer simulations.
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    AIChE Journal 42 (1996), S. 204-213 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Simultaneous effects of physisorption, diffusion, and reaction were characterized by dynamic experiments for propene metathesis over rhenium oxide/γ-alumina catalyst in a Berty reactor. Single-component sorption isotherms from steady-state experiments for ethene, propene, and 2-butene were used to predict multicomponent physisorption by the ideal adsorbed solution theory. Effective diffusivities were determined from molecular, Knudsen, and surface-diffusion coefficients, including bimodal pore-size effect and tortuosity factors. Transient sorption diffusion experiments were conducted with inactivated catalysts. The reaction rate expression, derived from elementary steps of carbene mechanism, was identified by solving the inverse problem with step test data. The direct problem was solved by orthogonal collocation within the method of lines. Model predictions agreed with responses from dynamic experiments carried out under conditions different from those used for estimating model parameters.
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    AIChE Journal 42 (1996), S. 239-248 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A thermodynamic framework is developed for calculating wax precipitation in petroleum mixtures over a wide temperature range. The framework uses the experimentally supported assumption that precipitated wax consists of several solid phases; each solid phase is described as a pure component or pseudocomponent that does not mix with other solid phases. Liquid-phase properties are obtained from an equation of state. Calculated wax-precipitation data are in excellent agreement with experimental results for binary and multicomponent hydrocarbon mixtures, including petroleum.
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    AIChE Journal 42 (1996), S. 269-270 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 290-295 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 285-289 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
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    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 296-297 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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    AIChE Journal 42 (1996), S. 301-318 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Experiments conducted quantify the macroscopic hydrodynamic characteristics of various scale 2-D bubble columns, which include dispersed and coalesced bubble regimes characterized by two flow conditions (4- and 3-region flow) with coherent flow structures. Hydrodynamic behavior is analyzed based on flow visualization and a particle image velocimetry (PIV) system. Columns operated in the 4-region flow condition comprise descending, vortical, fast bubble and central plume regions. The fast bubble flow region moves in a wavelike manner, and thus the flow in the vicinity of this region is characterized macroscopically in terms of wave properties. In columns greater than 20 cm in width, the transition from the dispersed bubble flow regime to the 4- and then to 3-region flow in the coalesced bubble regime occurs progressively with gas velocities at 1 and 3 cm/s, respectively. The demarcation of flow regimes is directly related to measurable coherent flow structures. The instantaneous and time-averaged liquid velocity and holdup profiles provided by the PIV system are presented in light of the macroscopic flow structure in various 2-D bubble columns. Numerical simulations demonstrate that the volume of fluid method can provide the time-dependent behavior of dispersed bubbling flows and account for the coupling effects of pressure field and the liquid velocity on the bubble motion. Comparison of computational results with PIV results for two different bubble injector arrangements is satisfactory.
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    AIChE Journal 42 (1996), S. 347-358 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The velocity and pressure fields and the effect of wall flux on these fields in a spiral channel are presented. As fluid flows inward through a spiral channel with constant gap and permeable walls, the streamwise flux decreases while the curvature increases. Thus, by balancing the stabilizing effect of wall suction with the destabilizing effect of increasing curvature, established vortices can be maintained along the spiral channel. This approach is used to prescribe spiral geometries with different wall fluxes. Using a weakly nonlinear stability analysis, the influence of wall flux on the characteristics of Dean vortices is obtained. The critical Dean number is reduced when suction is through the inner wall only, is slightly reduced when suction is equal through both walls, and is increased when suction is through the outer wall only. The magnitude of change is proportional to a ratio of small numbers that measures the importance of the effect of curvature. In membrane filtration applications the wall flux is typically 2 to 5 orders of magnitude less than the streamwise flow. If the radius of curvature of the channel is of the order of 100 times the channel gap, the effect on the critical Dean number is within 2% of the no-wall flux case. If the radius of curvature is sufficiently large, however, it is possible to observe effects on the critical Dean number that approach O(1) in magnitude for certain parameter ranges.
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    AIChE Journal 42 (1996), S. 383-390 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Multiple diffusion reactions are frequently encountered in the modeling of heterogeneous catalytic reactors. Obtaining an accurate estimate of the yield and selectivity in such reactions is crucial for an optimal design of reactors. Due to the inadequacy of analytical techniques in handling nonuniform catalyst shapes and mixed boundary conditions, numerical techniques are often employed to compute these design parameters. Among other numerical techniques, the boundary element method (BEM) is a superior method to solve linear diffusion reaction problems. The integral nature of the BEM formulation allows for boundary-only discretization of the particle, thus reducing the computer execution time and the data preparation effort. A boundary element algorithm is developed to solve a network of linear diffusion reactions in porous catalyst particles in two dimensions. For this purpose, a matrix of fundamental solutions is defined and derived. The developed algorithm is applied to complex reaction networks to obtain the yield of intermediates for nonregular catalyst shapes and nonuniform boundary conditions. The method can be used as a design tool to study particle scale modeling in detail and can be incorporated into an overall reactor model.
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    AIChE Journal 42 (1996), S. 409-421 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A novel gas purification technique called rapid pressure swing absorption (RAPSAB) was developed by integrating the best features of membrane contacting, gas-liquid absorption, and pressure swing adsorption (PSA). In this cyclic separation process, a well-packed microporous hydrophobic hollow-fiber module was used to achieve nondispersive gas absorption from a high-pressure feed gas into a stationary absorbent liquid on the module shell side during a certain part of the cycle followed by desorption of absorbed gases from the liquid in the rest of the cycle. The total cycle time varies between 20 s and upwards. Separation of mixtures of N2 and CO2 (around 10%) where CO2 is the impurity to be removed was studied using absorbent liquids such as pure water and a 19.5% aqueous solution of diethanolamine (DEA). Three RAPSAB cycles studied differ in the absorption part. Virtually pure N2 streams were obtained with DEA as absorbent demonstrating the capability of bulk separation to very high levels of purification. Numerical models developed predict the extent of purification for pure water and the DEA solution for one of the simpler cycles. Model simulations describe the observed behavior well.
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    AIChE Journal 42 (1996), S. 493-502 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Neural-network-based control schemes are generally designed by replacing standard elements of the classic control schemes by feedforward neural networks. The introduction of discrete time recurrent networks, which are inherently dynamic systems, into those schemes can simplify the design of neural controllers. The concept of applying recurrent networks in indirect adaptive control schemes is described. A combined network cluster consisting of the control network and the model network is constructed to allow the use of the real-time recurrent learning algorithm. To demonstrate the feasibility of the method two simulation examples are presented.
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    AIChE Journal 42 (1996), S. 516-523 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The one-sided single-pellet dynamic technique introduced in this article is shown to be a very effective and simple method for the analysis of adsorption and diffusion in porous solids. Moment expressions are presented for reversible and irreversible adsorption processes. Since the adsorption equilibrium constant is the only unknown parameter in the first moment expression, this parameter can be evaluated from a single set of pulse-response experiments. This technique to evaluate the adsorption equilibrium constant is illustrated using ethylbromide as tracer. It is also shown that for a very strongly adsorbing tracer, such as 1,2-dichloroethane in soil, modified moment expressions derived with a semiinfinite boundary condition are necessary unless a criterion developed in this work is satisfied.
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  • 91
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    AIChE Journal 42 (1996), S. 538-546 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Nuclear magnetic resonance (NMR) spin-lattice relaxation measurements are used to investigate pore structures and fluid phase distributions in porous media. A new method for estimating relaxation time distribution functions from measured relaxation data is presented using a B-spline basis to represent the distribution function and Tikhonov regularization to stabilize the estimation problem. Surface relaxivity, which is required to convert relaxation time distributions to pore-size distributions of fluid phase distributions at partial saturations, is determined using pore volume-to-surface-area ratios estimated by NMR diffusion measurements. This approach was validated by analyzing certain model porous media with known pore volume-to-surface-area ratios. The method is demonstrated by determining pore-size and fluid phase distributions of sandstone and carbonate samples, as well as by comparing the pore-size distributions of chalk samples obtained by this methodology with those estimated by mercury porosimetry.
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  • 92
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    AIChE Journal 42 (1996), S. 571-584 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The recently developed formalism for describing the solute-induced effect in dilute near-critical mixtures is extended to fluids composed of anisotropic molecules through the statistical mechanical interpretation of the derivative (∂P/∂x2)T,p∞ whose critical value is the Krichevskii parameter.Rigorous expressions for Henry's constant and the solute distribution factor along the orthobaric curve are derived in terms of the volumetric and entropic solute-induced local effects, and the quasi-linear behavior of their orthobaric density dependence away from the solvent's critical point is rationalized.The formalism is illustrated with integral equation calculations of the orthobaric density dependence of several solvation thermodynamic quantities for an infinitely dilute volatile solute in near-critical solutions of hard-sphere Yukawa fluids.
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  • 93
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    AIChE Journal 42 (1996), S. 649-659 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Drop breakup mechanisms inside a cavity flow are presented for two immiscible fluids. Due to the nonuniform flow condition of the cavity, the breakup mechanism varied along the streamlines. The streamlines were characterized by stream zones A and B, where zone A possessed a methodical transient breakup governed by Tomotika's breakup via capillary instabilities, and the breakup mechanism of stream zone B consisted of tip streaming breakup, an inefficient breakup mechanism. The flow behavior near flight region had a significant role in the drop breakup mechanisms. The study of the evolution of drop dispersion showed that the matrix viscosity is critical in controlling the transient breakup process and that the shear rate increase had little or no effect on the drop breakup.
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  • 94
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    AIChE Journal 42 (1996), S. 671-682 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The absorption of Cl2 into aqueous bicarbonate and aqueous hydroxide solutions was studied both experimentally and theoretically. The rate coefficient of the reaction between Cl2 and OH- was estimated over the temperature range of 293-312 K and fitted by the Arrhenius equation: \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{24} = 3.56*10^{11} \exp \left({\frac{{ - 1,617}}{T}} \right) $$\end{document}.If Cl2 were assumed to react only with water and OH- in an aqueous bicarbonate solution, the predicted absorption rate would be much lower than that experimentally measured. This suggests that Cl2 reacts with HCO3- in an aqueous bicarbonate solution. The rate coefficient of the reaction between Cl2 and HCO3- was estimated over the temperature range of 293-313 K and fitted by the Arrhenius equation: \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{21} = 5.63*10^{10} \exp \left({\frac{{ - 4,925}}{T}} \right) $$\end{document}.More importantly, under absorption conditions, the amount of hydroxide consumed for absorbing a specific amount of Cl2 into an aqueous hydroxide solution is almost twice the amount of bicarbonate consumed for absorbing the same amount of Cl2 into an aqueous bicarbonate solution.
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  • 95
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    AIChE Journal 42 (1996), S. 727-741 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A new discretization procedure for the agglomeration equation is presented. The intrinsic problems caused by discretization of the particle-size distribution are mitigated by using proper probability functions. Thus, the new discretized equation predicts the same total number of particles as its continuous counterpart and guarantees conservation of mass. This general method can correctly predict any two properties simultaneously and is not limited to number and mass. Simulation results with various agglomeration kernels show that the new method provides significant improvements over the conventional discretization method. Furthermore, the new method allows the user to choose equal-size intervals or geometric-size intervals with any geometric ratio to cover the particle-size range. In addition to flexibility, the latter feature leads to better accuracy in particle-size distribution predictions.
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  • 96
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    AIChE Journal 42 (1996), S. 753-766 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A new methodology for gage control of sheet and film processes is presented. A linear process model is developed that is capable of describing many of the interesting features of the process, including a noisy and moving gage sensor, significant process noise, strong coupling between the gage in different lanes, constraints on the actuators, and significant time delay between the actuators and the sensor. An automatic control of this process given this model form is designed. Novel features of the controller are that it can contend with information from a moving sensor and handle hard constraints on the actuators. Control performance and robustness to noise are demonstrated favorably via simulations.
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  • 97
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    AIChE Journal 42 (1996), S. 809-819 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A general theory for the adsorption of self-associating molecules in microporous structures is developed. The approach is similar to the “chemical” interpretation of nonideality of vapor and liquid phases. The theory displays Type 5 isotherm behavior and can explain Types 1 and 5 transition. Isothermal data are represented by only three parameters: Henry's law constant, saturation capacity, and reaction constant for “cluster” formation in the micropores. When isotherms at different temperatures are available, the theory can be used with five temperature-independent parameters to describe the entire phase behavior including the heat of adsorption. Water adsorption on activated carbon, the most common display of Type 5 behavior, is used to test the theory. Analysis of several data sets indicates that the theory can closely correlate data, provide physically meaningful parameter values in line with carbon properties, and it is highly effective in correlating temperature variation. The reaction enthalpy for water dimerization in the carbon micropores is lower than that in vapor phase. This preliminary conclusion with the theory needs to be supported with more accurate data when available.
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  • 98
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    AIChE Journal 42 (1996), S. 829-836 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Many living organisms store iron in solid form, Fe(III), as a crystal in the inner cavity of the ferritin molecule. When iron is needed for biosynthesis, a reducing agent reduces Fe(III) into the soluble form Fe2+ released by ferritin. Crystallization and release processes are reversible, and their rates evolve in an identical way as a function of the number n of iron atoms in the molecule. The rate increases with n, showing a maximum value when n is approximately 1,300, and then stabilizes for the highest values of n, which can reach 4,500. On the other hand, plotting the amount of released iron as a function of time gives curves with a sigmoid shape. The proposed model was based on the theoretical description of different steps involved in crystal growth inside the protein shell: several independent crystals grow freely at the inner protein wall, and then a distribution function takes into account possible overlapping of different crystallite clusters, whose further growth is limited by diminution of the available space inside the cavity. The kinetics derived was then used to calculate the release curve as a function of time. Solving the system of differential mass-balance equations was simplified by describing the ferritin population as a large discrete distribution of species. The model fully fitted and explained the variation in the crystallization rate with n, and the sigmoid shape of the release curve as a function of time obtained experimentally in a thin-layer electrochemical cell.
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  • 99
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    AIChE Journal 42 (1996), S. 850-860 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Cartilage constructs were grown using isolated chondrocytes and biodegradable polymer scaffolds made of fibrous polyglycolic acid in the form of 1-cm-dia × 5-mm-thick discs. The scaffolds were seeded in a mixed cell suspension and cultured for up to 8 weeks under static or mixed tissue culture conditions in petri dishes and spinner flasks. Turbulent mixing significantly improved the biochemical compositions and altered morphologies of the cartilage constructs, which were the thickest ones cultured to date in vitro. Constructs from mixed cultures were more regular in shape and contained up to 70% more cells, 60% more sulfated glycosaminoglycan, and 125% more total collagen when compared to constructs from static cultures. Mixing also induced the formation of an outer capsule with multiple layers of elongated cells and collagen fibrils around the inner tissue phase, while statically grown constructs consisted of round cells embedded in cartilaginous matrix. Mixing during cell seeding and tissue culture is thus an important parameter for the cultivation of tissue-engineered cartilage in a range of sizes, shapes and compositions for a variety of clinical applications (e.g., fibrous cartilage for reconstructive surgery or articular cartilage for joint resurfacing).
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    AIChE Journal 42 (1996), S. 889-891 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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