ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 261-270 
    ISSN: 0887-624X
    Keywords: chemically modified polymers ; addition reactions ; carboxybetaines ; reaction mechanisms and kinetics ; pyridines ; imidazoles ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed study of the synthesis of betaine products that result from addition reactions of poly (4-vinylpyridine) and poly (N-vinylimidazole) as well as of their model compounds, with α,β-unsaturated monocarboxylic acids is presented. A reaction mechanism based on experimental observations and proved by kinetic analysis is proposed. It consists of two reactions: the addition, which involves two molecules of acid and leads to X+B--like structures, where the cation X+ results from the addition of the amino nitrogen to the double bond of acid and B- is the carboxyl anion, and an equilibrium reaction between X+B- and the betaine structure X±. The latter occurs only in protic solvents and is coupled with the addition reaction. The process was especially investigated in methanol, because this solvent allows determination of the kinetic parameters. Some values of the addition rate constants are given. The study is based on 1H-NMR measurements and observations. © 1996 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1615-1623 
    ISSN: 0887-624X
    Keywords: chemically modified polymers ; addition reactions ; unsaturated betaines ; reaction kinetics ; pyridine ; imidazole ; photocrosslinking polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Unsaturated macromolecular carboxybetaines were obtained by reaction of poly(4-vinylpyridine) and poly(N-vinylimidazole) with propiolic acid. A kinetic model was presented for 4-methylpyridine. It consists of three coupled reactions: neutralization, addition which involves two molecules of acid and leads to a cation-anion pair structure, where the cation results from the addition of the amine nitrogen to the triple bond of acid, and an equilibrium reaction between the ion-pair structure and the betaine structure. The addition rate was found to be higher for poly(4-vinylpyridine) than for poly(N-vinylimidazole); it was also higher in water than in a water-methanol mixture. The reaction with acetylenedicarboxylic acid was carried out on poly(N-vinylimidazole), but the transformed units showed the structure that results from propiolic acid. The betaine products from 4-methylpyridine did not polymerize by radical initiation. The polymeric products show characteristics of photocrosslinking polymers. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1615-1623, 1998
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 389-398 
    ISSN: 0887-624X
    Keywords: chemically modified polymers ; addition reactions ; carboxybetaines ; proton magnetic resonance ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of vinylpyridine polymers with α,β-unsaturated carboxylic acids such as acrylic, methacrylic, crotonic, itaconic, cinnamic, fumaric, and maleic acids were studied. It was found that, when reacted with acrylic, itaconic and fumaric acids. poly(4-vinylpyridine) gave macromolecular betaine products while with maleic acid, betaine as well as the corresponding salt was obtained. Poly(2-vinylpyridine) reacted with the same acids as poly(4-vinylpyridine) gave only the salts. No significant changes were observed with the two polymers when reacted with methacrylic, crotonic, and cinnamic acids. To attempt to rationalize these observations with the two macromolecular tertiary amines, the reactions of 4-methyl and 2-methylpyridines with the same carboxylic acids were investigated. The 1H-NMR methodology was generally applied to elucidate the chemical structure obtained. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 3485-3494 
    ISSN: 0887-624X
    Keywords: polyanion-polycation complexes ; conductivity ; specific viscosity ; endpoint ; Ponceau 4R ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of some water-insoluble synthetic polyelectrolyte complexes formed between a weak polyanion and a strong polycation was followed. Sodium salts of poly(acrylic acid) and of some copolymers of acrylic acid with itaconic acid or maleic acid were used as anionic polymers. Cationic polyelectrolytes with quaternary ammonium salt groups in the main chain were used as strong polycations. The cationic polymers were different as concerns both the content of quaternary nitrogen atoms and the degree of branching. The complex formation was followed by the variation of the conductivity and of the specific viscosity of the reaction medium as well as by the turbidimetric titration versus the unit molar ratio polyanion/polycation. The deviation of the endpoint from stoichiometry was influenced mainly by the structure of the complementary polymers and by their molecular weights. The greater the structural differences, the higher the endpoint deviation from stoichiometry. Only insoluble polyelectrolyte complexes (PEC) were obtained in all the polyanion/polycation systems taken into account. The PECs were separated and characterized by elemental and spectral analyses as compared with the complementary polymers. © 1996 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The sorption of phenol, p-toluenesulfonic acid (p-TSA), Na-p-toluenesulfonate (Na-p-TS), 1,2-dihydroxy-3,5-benzene disulfonic acid disodium salt (Tiron), and 3-hydroxy-4(sulfonaphthyazo)-5,7-naphthalenedisulfonic acid trisodium salt (Poceau 4R) on the macroporus anion exchangers with acrylamide structural units (weak and strong basic anion exchangers) and on the ion exchangers with amidoxime groups were studied. The maximum specific sorption of p-TSA was almost identical with the total exchange capacity for both the weak and strong basic anion exchangers. The sorption of Na-p-TS is strongly related to the functional group structure of the anion exchangers, being significant on the strong basic anion excahngers. The maximum specific sorption of Tiron was higher tan the total exchange capacity of the strong basic anion exchangers because it is mainly dependent on the ionic exchange properties. The morphological characteristics influenced only the establishement rate of the sorption equilibrium. The sorption of Ponceau 4R, which has the highest molecular weight, is important on the strong basic anion exchangers with high permanent porosity. The sorption of the organic anions is also dependent on the number of the sulfonic groups. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Copolymers of 4-vinylpyridine : divinylbenzene with various degrees of crosslinking have been obtained as precursors for ionic polymers. To this end, addition reactions of the 4-vinylpyridine : 8% divinylbenzene copolymer to electrophylic ethylenic compounds, such as acrylamide, acrylonitrile, and methyl vinyl ketone in the presence of HCl have been performed; the resulting ionic polymers contain, besides ammonium quaternary groups, other functional groups such as amide, nitrile, and ketone. The quantitative iron retention from aqueous Fe2(SO4)3 solutions was determined photocolorimetrically for both 4-vinylpyridine : divinylbenzene copolymers and the synthesized ionic polymers. IR and Mössbauer spectroscopy were used to determine the state of the Fe(III) ions in the tridimensional networks. As expected, in 4-vinylpyridine : divinylbenzene copolymers, Fe(III) ions are retained by nitrogen atoms-Fe(III) complexes. The electronic state of metal ions hardly depends on the crosslinking degree. In the ionic polymers, the Fe(III) ions are retained through ionic exchange as the R4N+[Fe3(SO4)2(OH)6]- complex anion. The functional amide, nitrile, and ketone groups, although containing atoms able to form donor-acceptor bonds, do not take part in the complexation. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 2417-2427 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The behavior of various strong basic type II macroporous anion exchangers against the sorption of some organic acid alkaline salts as follows: natrium benzoate, natrium benzenesulfonate, potassium α-naphthylacetate, natrium β-naphthalenesulfonate, and natrium anthraquinone-2-sulfonate was established. The values of the sorption capacities depend on the morphology of anion exchanger network, the type and the size of organic anion, as well as the type of anion exchanger.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Several macroporous styrene-divinylbenzene copolymers were prepared using different diluents. The copolymers were chloromethylated with monochlor methyl ether and aminated with N,N-dimethyl-2-hydroxyethylamine in order to perform strongly basic anion exchanger, type II. It was established that the network morphology of anion exchanger determines its ion-exchange rate. It was, also established, by means of transmission electron microscopy, that chloromethylation reaction led to the morphological changes in the macromolecular network of the copolymers.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 222 (1994), S. 1-11 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Verschiedene Poly(vinyltoluol-co-divinylbenzol)-Netzwerke (VT-DVB), Vorstufen für ionische Polymere, wurden hergestellt und charakterisiert. Der Einfluß der Art des Verdünners und des Gehaltes an Divinylbenzol (DVB) auf die Copolymereigenschaften wird diskutiert. Sowohl expandierte als auch poröse Strukturen lassen sich leicht herstellen. Expandierte Strukturen bilden sich bei Verwendung guter oder schlechter Verdünner und geringen DVB-Konzentrationen, d.h. weniger als 20 Gew.-%, bezogen auf Vinyltoluol. Höhere DVB-Anteile ergeben makroporöse Strukturen. Auch die Möglichkeit der Herstellung stark basischer Anionenaustauscher aus den VT-DVB-Netzwerken wurden untersucht. Dazu wurden diese mit NaOCl/Phasentransferkatalysator chloriert und anschließend mit Trimethylamin oder N,N-dimethyl-2-hydroxyethylamin umgesetzt.
    Notes: Different poly(vinyltoluene-co-divinylbenzene) networks, precursors for ionic polymers, were synthesized and characterized. The influence of diluent nature and divinylbenzene (DVB) content on copolymer properties is discussed. Both expanded and porous structures can be easily prepared. Expanded structures are formed when good or poor diluents are used for low DVB content, i. e. less than 20 wt.-% with respect to vinyltoluene. Higher DVB content yields macroporous structures. Also, the possibility of obtaining strong base anion exchangers from poly(vinyltoluene-co-divinylbenzene) networks as precursors was investigated. Therefore, the above-mentioned networks were transformed by the chlorination reaction with NaOCI/phase transfer catalyst system, followed by the amination reaction with trimethylamine or N,N-dimethyl-2-hydroxyethylamine.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 269-275 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chlorometylation of linear and crosslinked polystyrene with 1,4-bis(chloromethoxy) butane was studied, and the behavior of 1,4-bis(chloromethoxy)butane in the presence of chloromethylation catalysts was also established by 1H-NMR spectroscopy.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...