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  • 1
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 7-13 
    ISSN: 0887-624X
    Schlagwort(e): radical terpolymerization ; charge transfer complexes ; phenanthrene ; maleic anhydride ; trans-stilbene ; thermal stability ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The radical terpolymerization of the donor-acceptor-donor monomer system, phenanthrene (P) - maleic anhydride (M) - trans-stilbene (S), was studied. These monomers are known to be nonhomopolymerizable. The terpolymerization was carried out in p-dioxane and/or toluene at 70°C in the presence of benzoyl peroxide used as the initiator. P and S were found to form charge transfer complexes (CTC) with M in p-dioxane at 35°C. The results obtained are discussed in terms of the free monomer and complex propagation models. It is shown that terpolymerization is carried out at a stage close to binary copolymerization of two complexomers. The reactivity ratio of P … M and S … M complexes was estimated by the Kelen-Tüdös method. Absorbance ratios at 1770 cm-1 (vC=0 of anhydride group), 764 cm-1 (δCH in monosubstituted benzene of S), and 820 cm-1 (δCH in disubstituted benzene of P) as a function of terpolymer composition were established. P - M - S terpolymers are shown to have high thermal stabilities. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1447-1454 
    ISSN: 0887-624X
    Schlagwort(e): terpolymerization ; charge transfer complex ; allylglycidyl ether ; maleic anhydride ; methyl methacrylate ; thermo-crosslinking ; photo-crosslinking ; thermal degradation ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Radical copolymerization of donor-acceptor monomers, i.e., allylglycidyl ether (AGE), maleic anhydride (MA) and methyl methacrylate (MMA) are studied, where binary copolymerization of AGE...MA complex with MMA is obtained. Constants of charge transfer complex formation (Kc) and copolymerization (r1 and r2) are determined by 1H-NMR and Kelen-Tüdöş methods, respectively. It is found that synthesized film-forming terpolymers with free epoxy and anhydride groups on side chain of macro-molecules are being crosslinked easily under the effect of temperature and/or UV-ir-radiation. Observed crosslinking effect is proved by the DTA, TGA, and IR spectroscopic analyses. It is shown that complex-radical terpolymerization is very convenient method for the designing of reactive functional macromolecules of linear structure with self-crosslinking properties which can serve as a basis for the use in photolithographic applications. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1501-1508 
    ISSN: 0887-624X
    Schlagwort(e): copolymerization ; charge transfer complex ; cyclization ; allyl acrylate ; allyl methacrylate ; maleic anhydride ; chain growth reactions ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Radical copolymerization of allyl acrylate (AA) and allyl methacrylate (AMA) as bifunctional monomers of donor (allyl)-acceptor (acryl) type with maleic anhydride (MA) as an acceptor monomer were carried out in metrhyl ethyl ketone (MEK) at 50-70°C in the presence of 2,2′-azoisobutyronitrile (AIBN) as initiator. Constants of complex formation (Kc), cyclization (kcl), and copolymerization (r1, r2, r1c, r1c1, and r1c2) as well as energies of activation for cyclization (Eac) and copolymerization reactions (Ea), and orders for the monomer (m) and initiator (n) concentrations were determined. The following values were found, for AA and AMA, respectively: Kc = 0.038 and 0.11 L/mol in deutered acetone at 35 ± 0.1°C, kcl = 6.45 and 6.53, r1 = 0.083 ± 0.005 and 0.028 ± 0.002, r2 = 0.027 ± 0.002 and 0.063 ± 0.003 (by the Kelen-Tüdös method), r1c = 0.04 and 0.025, r1c1 = 0.128 and 0.176, r1c2 = 0.127 and 0.177 (by the Seiner-Litt equation), Eac = 28.9 and 28.7 kJ/mol, Ea = 67.0 and 87.9 kJ/mol, m = 1.53 and 1.45, and n = 0.50 and 0.52. The presence of cyclic, unsaturated, and anhydride fragments in the macromolecules was confirmed with FTIR data and chemical (iodometrical and potentiometric titrations) analysis. It was established that complex formation in the monomer systems studied is the main factor for alternating cyclocopolymerization leading to formation of copolymers containing lactone and linear-unsaturated fragments in the macromolecular chain. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1501-1508, 1998
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 849-857 
    ISSN: 0887-624X
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Mechanisms of radical copolymerization of di-n-butylstannyl dimethacrylate with maleic anhydride in the presence of 2,2-asobisisobutyronitrile are discussed. Complexing (Keq) and copolymerization (r1 and r2) constants have been determined. Quantitative contributions of cyclization and complexing to reactivity ratios of the monomers under study and to propagation reactions have been estimated. The copolymerization has been found to proceed predominantly at the complex radical cyclocopolymerization step, leading to cyclized and linear unsaturated units in the macromolecule chain.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2339-2345 
    ISSN: 0887-624X
    Schlagwort(e): copolymerization ; photocross-linking reaction ; photosensitivity ; quantum efficiency ; organotin copolymer ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Radical-initiated copolymerization of tri-n-butylstannyl methacrylate (TBSM) with allyl chloroacetate (ACA) was carried out in the presence of benzoyl peroxide as initiator in benzene at 70°C in nitrogen atmosphere. Monomer reactivity ratios of the TBSM (M1)-ACA (M2) monomer pair were determined by the Kelen-Tüdöş method: r1 = 1.25 ± 0.02 and r2 = 0.13 ± 0.005. From copolymerization kinetic data the values of effective energy of activation (Ea) and orders with respect to initiator (n) and to monomers (m), Ea = 79.0 kJ/mol, n = 0.51, and m = 1.2, were determined. Photochemical reactions of the copolymer were studied by using monochromatic UV-irradiation at 405 nm and FTIR spectroscopy. For the copolymer synthesized the quantum efficiency (φcrl = 0.62 mol/Einstein) and photosensitivity S = 25.5 cm2/J (in the presence of 1,9-dibromoanthracene as a sensitizer) were found. It was shown that the effects observed of the tin atom and Cl substituent via pentacoordinated complex ( - R3Sn…O=C - ) and σ(Cl - CH2)-π(C=O)-π(allyl) conjugation, respectively, are the main factors for reducing degradative chain transfer and for increasing the tendency of monomers to alternate as well as for the photocrosslinking of copolymer macromolecules. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2339-2345, 1998
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 21 (1990), S. 459-463 
    ISSN: 0933-5137
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Maschinenbau
    Beschreibung / Inhaltsverzeichnis: Structure and Properties of a High Strength Spray-Deposited Aluminum Alloy A 7XXX series high strength aluminium alloy was produced by spray-deposition via the Osprey process. This alloy, designated A1Zn11MgCu, exhibits an excellent combination of fracture toughness and strength in both the peak-aged T6 temper and the overaged T7 temper. The yield strength and fracture toughness at room temperature are in the T6 temper 700 MPa and about 40 MPa√m, and in the T7 temper 500 MPa and 75 MPa√m, respectively.The exceptional high fracture toughness is attributed to the absence of coarse constituents and oxides. The microstructure is homogeneous, free of segregation and has a fine grain size. The hardening precipitates in the T6 temper are mainly η′, and the T7 temper they are η (MgZn2), resulting in a different fracture behavior: in the T6 temper the fracture mode is micro-shearing and in the T7 temper fracture mode is ductile failure.
    Notizen: Die hochfeste sprühkompaktierte Osprey-Aluminiumlegierung vom Typ AlZn11MgCu weist sowohl im maximal ausgehärteten als auch im überalterten Zustand die beste Kombination aus Festigkeit und Bruchzähigkeit aller heute bekannten hochfesten Aluminiumlegierungen auf. Im Zustand T6 erzielt man bei Raumtemperatur Streckgrenzenwerte von über 700 MPa bei einer Bruchzähigkeit von knapp 40 MPa√m, im Zustand T7 liegen die Werte bei 500 Mpa bzw. 75 MPa√m.Entscheidend für die hohen Bruchzähigkeitswerte ist, daß im Gefüge keine groben bruchauslösenden Phasen und Oxide vorliegen. Die struktur ist homogen, seigerungsfrei und feinkörnig. Die festigkeitssteigernden Aushärtungsphasen sind im Zustand T6 überwiegend teilkohärente η′-Teilchen und im überalterten Zustand T7 inkohärente η-Teilchen (MgZn2). Demzufolge ist das Bruchverhalten unterschiedlich. Im Zustand T6 tritt Mikro-Scherbruch auf, im Zustand T7 duktiler Grübchenbruch.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 21 (1990), S. 221-229 
    ISSN: 0933-5137
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Maschinenbau
    Beschreibung / Inhaltsverzeichnis: Verschleißminderung im mit Kohleslurry betriebenen Großdieselmotor dank werkstofftechnischer ModellierungBei Großdieselmotoren mit Kohleslurry als Brennstoff fällt bei der Verbrennung relativ viel abrasive Asche (Eisenoxide, Quarz) an. Ziel dieser Arbeit war, die Laufflächen von solchen Motoren - insbesondere die Kolbenringe und den Zylindereinsatz - so weit verschleißbeständig zu machen, daß ähnliche Lebensdauern wie bei der Verwendung von aschefreien Brennstoffen resultieren.Aufgrund von Betriebsversuchen konnte die Verschleißbeanspruchung als vorwiegend abrasiv eruiert werden. Dazu wurde als neuartige werkstofftechnische Lösung ein Zermalmen der Ascheteilchen beim Eintritt in den Schmierspalt auf eine unterkritische Größe gefunden. Dazu müssen alle betroffenen Laufflächen mit der gleichen hochabrasionsbeständigen Randschicht versehen werden: Harte, zähe Matrix und etwa 30-70° Hartphasenanteil mit Korngrößen von 30-200 m̈m und minimaler Härte von etwa 2000 HV.Die über Pulver aufgebaute und metallurgisch gebundene Schicht besteht aus einer chrom- und molybdänhaltigen Matrix mit austenitisch-martensitischer Gefügeausbildung, in die Titan-, Vanadin- und/oder Wolfram-Grobkarbide eingebettet sind.Erste Abrasionstests bestätigen die Richtigkeit unserer Verschleißhypothese und unseres Werkstoffmodells.
    Notizen: In the combustion of coal slurry as fuel in large-bore diesel engines, a relatively large amount of abrasive ash occurs (iron oxides and quartz). The object of this work was to make the running surfaces of such engines - especially the piston rings and cylinder liner - so resistant to wear that service life similar to that using ash-free fuels is obtained.Based on result of operational wear stressing tests wear damage was identified as mainly abrasive. A novel materials solutions is to crush the ash particles to a subcritical size when they enter the lubrication gap. For this, all running surfaces involved must be provided with the same surface: a hard, tough matrix and about 30-70% hard phase with grain sizes of 30-200 m̈m and minimum hardness around 2000 HV highly resistant to abrasion.The layer built up with powder and bonded metallurgically consists of a matrix containing chromium and molybdenum, with austenitic/martensitic structure formation, in which titanium, vanadium and/or tungsten coarse carbides are embedded. Initial abrasion tests carried out on selected samples confirm the validity of our wear hypothesis and our material model.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 37 (1995), S. 119-128 
    ISSN: 0959-8103
    Schlagwort(e): plasma polymerization ; organosilicon monomers ; organotin monomers ; plasma kinetic parameters ; deposition rate ; structure ; thermostability ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Plasma polymerization of several selected saturated and unsaturated silicon- and tin-containing monomers, such as vinyltriethoxysilane (VTES), 3-aminopropyltriethoxysilane (APTS), hexamethyldisiloxane (HMDS), hexabutyldistannoxane (HBDS) and tetraethylstannane (TES), were examined in terms of the following selected plasma operational parameters: discharge time (t), flow rate of monomer (F) and power input (W). For the initial deposition rates (DR), the following empirical equation was proposed: DR = k ta Fb Wc, from which the experimental values of the kinetic power factors (a,b,c and k) were calculated. The value of k calculated for VTES was the highest, indicating the high activity of the monomer in plasma in contrast to HBDS, which was about two orders of magnitude smaller. A modified Arrehnius equation was employed in the form of yield of deposition (DR/F) versus the specific energy (W/F), which showed that silicon-containing monomers are more active than their organotin analogues in the chosen plasma conditions. Plasma polymers of HMDS, TES and HBDS prepared at low conversions were highly crosslinked and their structures were similar to those of crosslinked poly(dialkylsiloxane) or poly(organostannoxane) while those of VTES and APTS were primarily linear.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 259-265 
    ISSN: 0959-8103
    Schlagwort(e): copolymerization ; charge-transfer complex ; trans-stilbene ; N-maleimide ; N-ethylmaleimide ; N-phenylmaleimide ; structure ; thermal degradation ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Radical copolymerization of donor-acceptor monomers, i.e. trans-stilbene (Stb) with N-maleimide (MI), N-ethylmaleimide (EtMI) and N-phenylmaleimide (PhMI), are studied. Constants of charge-transfer complex formation (Kc) and copolymerization (r1 and r2) are determined by Hanna-Ashbaugh (1H nuclear magnetic resonance) and Kelen-Tüdöş methods, respectively. The results obtained were analysed by use of the complex copolymerization model of Seiner-Litt. It is found that the tendency for complex formation and the tendency for alternation of monomers depend on the nature of the N-substituent in the maleimide molecule. Kc is found to increase in the order EtMI 〈 MI 〈 PhMI, and the tendency for alternation (r1 · r2) decreases in the order MI 〉 EtMI 〉 PhMI. It is shown by thermogravimetric analysis, differential thermal analysis and differential scanning calorimetry that the alternating copolymers synthesized have high thermostabilities. The copolymers synthesized show increased thermal stabilities, as well as glass transition temperatures, with the change of imide N-substituent. Stb-MI, Stb-EtMI and Stb-PhMI copolymers decompose through a one-step reaction at 456, 460 and 468°C, respectively.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 59 (1996), S. 235-241 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Polystyrenes with different molecular weights were chemically modified with maleic anhydride by use of certain cationic catalysts of Lewis acid type (BF3·OEt2, AICI3, TiCL4, ZnCl2, FeCl3, and SnCl4) in chloroform. The effects of molecular weight of polystyrene, as well as type of Lewis acid used, on properties and structure of products were investigated. The interrelation between the molecular weight of polystyrene and content of carboxyl groups in the products was made. A direct relationship between the activity of catalyst used and the number of carboxyl groups was found. For characterization of side-chain functionalized polystyrene, fractional precipitation was applied which yielded carboxyl groups in all fractions. The carboxyl group concentrations were found to be the highest in the case of BF3·OEt2. Modified polystyrene samples containing —CO—CH=CH—COOH fragments in side chains are easily crosslinked at 140-150°C and by UV irradiation as proved by IR, DTA, and TGA analyses. Functionalized polymers obtained are characterized by their high thermostability, adhesion, and photosensitivity. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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