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  • Industrial Chemistry and Chemical Engineering  (20)
  • Wiley-Blackwell  (20)
  • American Institute of Physics
  • International Union of Crystallography (IUCr)
  • 1995-1999  (20)
  • 1975-1979
Collection
Publisher
  • Wiley-Blackwell  (20)
  • American Institute of Physics
  • International Union of Crystallography (IUCr)
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemical Engineering & Technology - CET 18 (1995), S. 440-444 
    ISSN: 0930-7516
    Keywords: Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Acidic zeolite LZ-M-8 was used to catalyse the hydrolysis reaction of inulin into fructose. Fructose contents of 96% and 75% were obtained when commercial inulin and Jerusalem artichoke extract were used respectively as substrates. Zeolite LZ-M-8 was found to be extremely selective towards inulin hydrolysis as compared to fructose decomposition. Formation of hydroxymethyl furfural (HmF) was not detected and it was confirmed that zeolite LZ-M-8 does not adsorb HMF. The catalytic activity of the zeolite remained intact upon repeated use of the catalyst. The superiority of the zeolite over other catalysts used in inulin hydrolysis was demonstrated experimentally.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Particle and Particle Systems Characterization 12 (1995), S. 188-193 
    ISSN: 0934-0866
    Keywords: Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The paper reports on the particle. sampling efficiency of the inlet system for the Aerodynamic Particle Sizer (TSI, Inc., St. Paul MN). Large particles are depleted from the sampled aerosol by two mechanisms: super-isokinetic sampling at the entrance of the inlet, and inertial impaction on the inner nozzle. A fluorometric technique was used to separately characterize these mechanisms. Numerical studies were also performed. The experimental results show that the inlet's overall efficiency drops from around 90% for 3 μm particles to less than 45% for particles larger than 10 gm. Several high efficiency inlets were developed and tested. These inlets provide higher sampling efficiencies, but reduce the instrument's sizing resolution. Measurements of 7.3 μm oleic acid particles with a high efficiency inlet showed a 5% spread in measured diameter at 50% count, while less than a 1076 spread was observed using the standard inlet. It was also found that the super-isokinetic condition reduces particle losses on the inner nozzle. The standard inlet is recommended for verifying test aerosol monodispersity. An alternative to the standard inlet is suggested for measurement of size distributions.
    Additional Material: 8 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Particle and Particle Systems Characterization 13 (1996), S. 234-237 
    ISSN: 0934-0866
    Keywords: Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Process Engineering, Biotechnology, Nutrition Technology
    Notes: This paper describes a study to determine the most appropriate particle size parameter for polydisperse powders dispersed as aerosol and detected by light scattering. It is relevant to many areas of engineering research. By means of calculations of the intensity of light scattered from particles of different sizes, it has been shown that the surface median aerodynamic diameter (SMAD) is an appropriate measure for polydisperse aerosolised powders. The microscope-based procedure for obtaining the SMAD is described, as well as its implementation for narrowly-graded polydisperse powders of fused alumina of type which have been widely used in studies of particle transport in wind tunnels. It was shown that for the fused alumina powders examined, SMAD = 1.25 x (PASMAD), where PASMAD is the projected area surface median aerodynamic diameter.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 643-650 
    ISSN: 0268-2605
    Keywords: tributyltin ; sediment ; degradation ; coastal British Columbia ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Butyltin concentrations in the sediments of two coastal areas of British Columbia, Canada, are reported. Two recent box cores from the deepest basin in the Strait of Georgia were sectioned and analyzed by GC-atomic emission spectrometry. No butyltin compounds were detected above 0.5 μgSn kg-1 (dry weight) in either core. These results are compared to those for a previous (1991) core from the same area. In that study, tributyltin (TBT) concentrations were in the range 1-2 μgSn kg-1 down the core and were higher than those of either of the degradation products, dibutyltin (DBT) and monobutyltin (MBT). Radioisotope dating (210Po-210Pb counting methods) was used to establish the rates of sedimentation of 0.25 and 2.6 cm y-1 at the two sites. Data suggest that a combination of rapid deposition of new, less-contaminated material and degradation of previously deposited butyltin compounds has resulted in the observed absence. Thirty-three surface sediments from the northern BC coastal harbor at Prince Rupert, collected in 1995, were analyzed for butyltin residues by GC-FPD. Concentrations of TBT, DBT and MBT were in the ranges from below the appropriate limit of detection (LOD) to 1262, to 109 and to 37 μgSn kg-1, respectively. TBT/DBT ratios ranged from 0.2 to 62 with most above unity, indicating that there is continuing fresh input of TBT. The sources are almost exclusively large ocean-going vessels that use the harbor for long-term anchorage. These findings are discussed with reference to the global TBT status. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 577-584 
    ISSN: 0268-2605
    Keywords: organotin ; extraction ; analysis ; GC-FPD ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of: (1) the modifier type (methanol and formic, acetic and propionic acids), (2) complexing agents (diethylammonium diethyldithiocarbamate, ammonium pyrrolidinedithiocarbamate) either with or without acidic modifiers, (3) the extraction temperature (50-80 °C) and pressure (30-50 MPa), (4) the extraction procedure (static-dynamic or dynamic), and (5) the volume of static modifier, on the extraction efficiency of native butyl- and phenyl-tin compounds from sediment, were evaluated comprehensively. The highest extraction efficiency for butyl- and phenyl-tin compounds was obtained at 30 MPa and 50 °C by using CO2 modified with acetic acid (200 μl in the cell). Supercritical fluid extraction (SFE) extracts were hexylated and determined by GC-FPD using a 610 nm bandpass filter without any clean-up step. In summary, the developed analytical procedure is robust (no restrictor clogging; free from FPD interferences), it is low-cost (no complexing agents needed), it has a high sample throughput (〈3 h), it is independent of the matrix for the determination of butyltin compounds in sediment, and it provides the highest precision among the SFE procedures reported for organotin determination. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 6 Ill.
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  • 6
    ISSN: 0268-2605
    Keywords: carbohydrate-modified phenylsiloxane ; surfactants ; wetting behaviour ; superspreading ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dynamic wetting behaviour on a perfluorinated, low-energy solid has been investigated for a carbohydrate-modified phenylsiloxane surfactant. The surfactant concentration, the rate of interface generation and the [solid/liquid interface area] : [liquid/vapour interface area] ratio were varied systematically. Dynamic data for the liquid/vapour (γlv) and solid/liquid (γsl) interfacial tension as well as their Lifshitz-van der Waals and donor-acceptor contributions were determined under strictly controlled conditions. Since γsl reacts sensitively to variations of the surfactant concentration and the rate of interface generation, the covering of the liquid/non-polar solid interface is assumed to be a spreading limiting factor. The corresponding γlv values remain constant and close to those obtained under equilibrium conditions. Copyright © 1998 John Wiley & Sons, Ltd.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 153-161 
    ISSN: 0268-2605
    Keywords: polyimides ; solution polycondensation ; seven-membered cyclic polyimide intermediate ; polyimide-silica gel hybrids ; sol-gel reaction ; pyrolysis ; pore size ; surface area ; adsorption-desorption isotherms ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A facile preparation of polyimide-silica gel hybrids by the simultaneous in-situ formation of polyimides during the hydrolysis-condensation of tetramethoxysilane (TMOS) is reported here. The hydrolysis and condensation of TMOS was carried out in a solution of DMAc containing 5% LiCl, CaCl2 or ZnCl2 and the seven-membered cyclic polyimide intermediate. The seven-membered cyclic intermediates, precursors of polyimides, were derived from the low-temperature polycondensation of dianhydrides [benzophenonetetracarboxylic dianhydride (BTDA), pyromellitic dianhydride (PMDA), and 4,4-bis(hexafluoroisopropylidene)phthalic dianhydride (6FDA)] and di-isocyanates [isophorone di-isocyanate (IPDI), toluene di-isocyanate (TDI), hexamethylene di-isocyanate (HDI) and 4,4′-diphenylmethane di-isocyanate (MDI)]. These intermediates could readily be converted to the corresponding polyimides. Films were cast from the resulting mixtures and the solvent was gradually evaporated at 130 °C to result in the formation of clear, transparent, pale yellow or amber-colored hybrid films in which the salts were dispersed at the molecular level. Pyrolysis of polyimide-silica gel hybrids at 600 °C gave mesoporous silica. Silica gel obtained from hybrids HPI-8 (containing no salt) and HPI-11 (containing ZnCl2) had a pore radius (BJH method) of 2.9 nm, while that from hybrid HPI-9 (containing LiCl) had a pore radius of 11.4 nm. The surface areas (BET method) obtained were 203 m2 g-1, 19 m2 g-1 and 285 m2 g-1, while the pore volumes were 0.373 cm3 g-1, 0.158 cm3 g-1 and 0.387 cm3 g-1, respectively, for samples obtained from hybrids HPI-8, HPI-9 and HPI-11. © 1997 by John Wiley & Sons, Ltd.
    Additional Material: 2 Ill.
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  • 8
    ISSN: 0268-2605
    Keywords: radiolabeling ; trimethylamine-carboxyborane ; trimethylamine-carboxymethoxyborane ; leukemic cell uptake ; binding to nucleic acids and protein ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The anti-neoplastic agents trimethylamine-carboxyborane and its corresponding methyl ester have successfully been radiolabeled with carbon-14 in the carboxyl group. Using the radiolabeled agents we have shown that their L1210 leukemia cell uptake appeared to be by a passive process and binding of the agents to DNA, RNA and protein over 24 h was minimal.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 577-581 
    ISSN: 0268-2605
    Keywords: dioxastannolanes ; antitumour ; human cell lines ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Six dibutyl-1,3,2-dioxastannolanes, including two enantiomeric pairs, exhibited greater in vitro antitumour activity towards a variety of human tumour cell lines than cisplatin but with little discrimination, suggesting hydrolysis to a common cytotoxic intermediate. A cell line hypersensitive to mitochondrial inhibitors (CI80-13S) was not sensitive to any of the test compounds, suggesting that cell mechanisms other than, or in addition to, mitochondrial function are targeted by tin antitumour agents. A pigmented melanoma cell line (MM418c5) was resistant to the test compounds, which were found to be sequestered by melanin. This resistance was not observed with triphenyltin hydroxide. © 1997 John Wiley & Sons, Ltd.
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  • 10
    ISSN: 0268-2605
    Keywords: siloxane ; surface tension ; control angle ; interfacial tension ; wetting tension ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The surface tensions, wetting tensions, contact angles and solid/liquid interfacial tensions of defined siloxanes as well as those of analogous carbosilanes, polysilanes and neopentyl substituted silanes were determined. The wetting experiments were carried out on a glass plate coated with perfluoroalkyl methacrylate (FC 722®). The siloxanes possess the lowest surface tensions. Due to the presence of oxygen atoms in the siloxane backbone, a donor-acceptor portion (γ+/-lv) of the surface tension of about 1-2 mN/m was determined. The solid/liquid interfacial tension also contains a donor-acceptor portion (γ+/-sl). Its value is almost identical to that of γ+/-lv. The γ+/-sl differences between individual molecules of the same surface tension are responsible for contact angle differences of up to 4°. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 6 Ill.
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