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1. |
Versuche zur pfropfung von polystyrol auf rußoberflächen |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 1-41
Dietrich Braun,
Axel Kamprath,
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摘要:
AbstractSchlagfeste Polystyrole auf der Basis von Polybutadienkautschuk als Elastomerkomponente besitzen im Vergleich zu Standard‐Polystyrolen eine deutlich reduzierte Witterungsbeständigkeit. Einer wirkungsvollen Stabilisierung dieser Werkstoffe mit feinverteiltem Ruß steht die Tatsache entgegen, daß infolge einer mangelnden Ruß‐Polymer‐Verträglichkeit das Pigment eine Kerbwirkung zeigt, die den Hauptvorteil des schlagfesten Polystyrols — seine hervorragende Zähigkeit — deutlich vermindert. In dieser Arbeit wird über Versuche berichtet, durch Aufpfropfen von Polystyrolketten auf die Rußoberflache eine Verbesserung der Ruß‐Polymer‐Verträglichkeit und damit der technologischen Eig
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200101
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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2. |
Incidence of heterogeneity due to polymer incompatibility on the reaction between telechelic prepolymers and on the mechanical properties of the multiblock copolymers formed |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 43-59
Philippe Chaumont,
Gérard Beinert,
Christian Prud'Homme,
Jean Herz,
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摘要:
AbstractThe polycondensation reaction between telechelic poly(dimethylsiloxanes) and α,ω‐difunctional polystyrenes (or substituted polystyrenes) in toluene solution is very fast, in spite of the heterogeneous nature of the reaction medium. In the first part of the article is reported a qualitative approach of the condensation reaction in relation to the microscopic structure of the reaction medium. The second part is devoted to an investigation of the mechanical and thermomechanical behaviour of the multiblock copolymers which results from intramolecular phase separat
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200102
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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3. |
Dielectric behaviour of styrene‐methyl methacrylate copolymer foams at microwave frequencies |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 61-72
Pranab C. Bandyopadhyay,
Ajit K. Banthia,
Tapan K. Chaki,
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摘要:
AbstractAmbient dielectric effects were studied by the short‐circuited waveguide method at 9.375 GHz microwave frequency in foams from copolymers of styrene and methyl methacrylate of varying compositions, generated under identical conditions of solvent‐nonsolvent ratio, impregnation time and steaming period. The results were correlated with foam‐density, porosity and composition and were interpreted in terms of dipole‐dipole interactions and the applicability of Wiener's inequalities, logarithmic law of Lichtenecker and Rother with an empirical factor of 0.64 in the index based on the additive law of mixtures and the Böttcher‐Bruggeman's relation. Scanning electron micrography on copper‐coated fractured surfaces of the samples was done in order to examine the degree of foamability, cell‐size distribution and the mechanism of failure. Microhardness, compressive and flexural strength were also measured. Loss characteristics were similarly ascribed to copolymer foamability and dipoleorientability. A prudent choice in the monomer reactivity ratio might therefore yield an optimum reinforcement and a proper dielectric requirement suitable for electronic and radar device
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200103
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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4. |
High yield catalysts in olefin polymerization. General outlook on theoretical aspects and industrial uses |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 73-90
Paolo Galli,
Pier Camillo Barbè,
Luciano Noristi,
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摘要:
AbstractThe new third generation Ziegler‐Natta catalysts give extremely high yield and produce highly stereoregular polypropylene of controlled morphology and size. The role of Lewis bases and MgCl2is underlined and their mechanisms of action is discussed in the light of the most significant experimental data. Furthermore, technological and economical advantages are emphasize
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200104
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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5. |
Viskosimetrische bestimmung des polymerisationsgrades von oxycellulose mit hilfe der EWNN‐methode |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 91-104
Jan Blaha,
Pavel Černý,
Karel Jahn,
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摘要:
AbstractFür die Bestimmung der Grenzviskositatszahl [η] von nitroso‐oxydierter Cellulose in verdünnter Losung wurde die EWNN Methode (alkalische Lösung eines Eisen‐Weinsäure‐Natrium‐Komplexes) angewandt. Die bisher bekannten Berechnungsmethoden von [η]mit Hilfe der Polynome für verschiedene Arten von Polymeren, verschiedene Lösungsmittel und Meßsysteme sowie auch für reine Cellulose erwiesen sich als unbrauchbar. Es wurde eine empirische Berechnungsformel in expliziter Form\documentclass{article}\pagestyle{empty}\begin{document}$$[\eta ] = \frac{{\eta _{{\rm sp}} }}{{\rm c}} + {\rm c}^2 + {\rm A}_1 \eta _{{\rm sp}} {\rm c} - \eta _{{\rm sp}}^2 {\rm c} + {\rm A}_2 \eta _{{\rm sp}}^3 {\rm c} + {\rm A}_3$$\end{document}mit A1= −2,348, A2= 3,584 und A3= 0,006 (ηsp: spezifische Viskosität, c: Konzentration g/100 ml) vorgeschlagen, die die Berechnung von [η] bei Oxycellulose aus einer bei einer einzigen Konzentration der Probe durchgeführten Messung ermöglicht. Für die Berechnung eines Mittelwertes für den Polymerisationsgrad nach der Staudinger‐Mark‐Houwink‐Gleichung war es möglich, die für nichtoxydierte Cellulo
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200105
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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6. |
Anwendung einer Näherungsmethode zur Verarbeitung der Zeit‐Umsatz‐Kurven |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 105-117
Alois Matějíček,
Josef Seidl,
Emil Krejcar,
Josef Matyáš,
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摘要:
AbstractIn einer vorausgegangenen Arbeit wurden Verfahren vorgeschlagen, die die Zeit‐Umsatz‐Kurven der chemischen Reaktion zwischen dem flüssigen Reaktanten und dem vernetzten makromolekularen Stoff auszuwerten ermöglichen. In dieser Arbeit werden die angeführten Verfahren an einem Beispiel der alkalischen Hydrolyse des Perlcopolymeren aus Acrylsäureethylester, Acrylnitril und Divinylbenzol beschrieben, weiterentwickelt und untereinander ver
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200106
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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7. |
Mechanisms of degradation of cotton and effects of mercerization‐stretching upon the course of these mechanisms, part VII. Characterization of microstructural differences between scoured cotton and slack mercerized‐stretched cottons |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 119-148
A. Hebeish,
A. Waly,
N. Y. Abou‐Zeid,
N. A. Ibrahim,
M. H. El‐Rafie,
A. T. El‐Aref,
A. Bayazeed,
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摘要:
AbstractConditions were established to introduce almost equal and reproduciple amounts of diethylaminoethyl (DEAE) substituents into the molecular structure of scoured cotton (substrate I), slack mercerized cotton (substrate II), slack mercerized‐stretched (94%, substrate III), and slack mercerized‐stretched (103%, substrate IV) cotton. Similarities between the original structures of these substrates before and after the chemical modification were assessed by X‐ray analysis. Comparison between the DEAE cottons and the corresponding unmodified cottons upon acid hydrolysis with respect to moisture regain, loss in weight and degree of polymerization was also made. Chemical analysis was used to study the compositions and structures of the hydrolyzates (i.e., hydrocelluloses and solublized fractions) resulting from hydrolysis of the modified cottons with 2.5 N HCl under reflux for different lengths of time. Studies of rates of hydrolysis of the cellulose, rates of removal of substituted glucoses and rates of removal of individual types of substituted glucose units were considered as means to provide information regarding: (a) distribution of DEAE substitutents throughout the structure of cellulose, (b) nature of accessible regions where the DEAE substituents are developed, and (c) selective availability of the hydroxyl groups at C‐2, C‐3 and C‐6 of the D‐glucopyranosyl units in the cellulose elem
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200107
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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8. |
Effect of copolymers modifying PVC on its physical and mechanical properties and its UV‐radiation resistance. III. Changes in thermal stability of PVC films modified by MMA/MA, VC/VAC, MBS or ABS induced by UV‐irradiation |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 149-154
A. Kamińska,
H. Kaczmarek,
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摘要:
AbstractThe influence of UV‐radiation on thermal stability of PVC films, depending on the type and quantity of modifying copolymers, was studied. It was found that UV radiation can induce various changes in thermal stability of PVC decreasing its dehydrochlorination temperature T01while increasing temperature of decomposition T02.Particularly distinct changes in sampels containing VC/VAC indicate that even 1% of this copolymer accelerates the photodehydrochlorination and the processes which decrease the temperature of decomposition of PVC.Smaller changes than in pure PVC in thermal parameters in samples containing ABS after irradiation show that this copolymer increases the PVC resistance to UV radiation.Films containing MBS, ABS, MMA/MA reveal the largest changes in T01after irradiation in the case of a content of 1% of these copolymers in the samples. In the case of bigger quantity (3 to 10%) the changes are smaller and may even diversify their direction. These copolymers, contrary to VC/VAC, make PVC films a little turbid indicating the limited compatibility of both components. Hence, the conclution is that the structure of a film, depending on compatibility of components and changing with their differing concentration, has decisive influence on the thermal and photochemical processe
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200108
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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9. |
Einfluß der adsorption von 3‐N‐alkylaminopropan‐1‐olen auf das zetapotential von polymeroberflächen |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 155-162
H. Kaden,
J. Beger,
R. Jacobi,
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摘要:
AbstractEs wird das Prinzip einer Meßanordnung zur Bestimmung von Zetapotentialen an plattenförmigen Polymeren vorgestellt. An Platten aus Polytetrafluorethen und Homopolystyrol wurden charakteristische Unterschiede des Zetapotentials nach der Adsorption von 3‐N‐Alkylaminopropan‐1‐olen und Dodecylpropylamin aus wäßriger Lösung nachgewiesen. Der Einfluß von pH‐Wert, Konzentration und C‐Kettenlänge der Tensid
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200109
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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10. |
Pyrolysis field desorption mass spectrometry of polymers. III. Aliphatic polyamides |
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Die Angewandte Makromolekulare Chemie,
Volume 120,
Issue 1,
1984,
Page 163-175
U. Bahr,
I. Lüderwald,
R. Müller,
H.‐R. Schulten,
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摘要:
AbstractPyrolysis field desorption mass spectrometry has been performed from various polyamides such as nylon 6, 8, 12, and nylon 66. The pyrolytic behaviour of these compounds depends strongly on the solvent and the temperature program employed. Using formic acid as solvent strong thermal fragmentation is observed, while with 1,1,1,3,3,3‐hexafluoro‐2‐propanol almost exclusively molecular ions or cationized molecules of the monomer building block M are produced. With increasing temperature larger clusters of polymeric subunits (Mn+ Na)+are generated, but thermal fragmentation on the emitter surface also increases. The cationized molecules dominate all spectra. They are found from M3to M5or M15depending on the chain length of the polymer subunit. With increasing temperature, the base peak of the spectrum is shifted to the higher mass end and small signals up to m/z 2000 and above are recorded. Thermal products are mainly formed by water elimination (−18 mu), loss of the acid amide group (−44 mu) after rearrangement and from longer polyamides by loss of the methylene groups (− 42 or 56 mu) by cis‐elimination.These thermal fragmentations of the polymeric substances on the emitter surface can be controlled by appropriate emitter heating and correlate directly with the common chemical knowledge of these materials in the liquid or solid phase. Together with the options of integrating recording, high mass resolution and direct isotope determination, the combination of pyrolysis and field desorption mass spectrometry offers a unique tool for characterization of building blocks and high mass sequences in synth
ISSN:0003-3146
DOI:10.1002/apmc.1984.051200110
出版商:Hüthig&Wepf Verlag
年代:1984
数据来源: WILEY
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