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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 45 (2000), S. 259-265 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: SUMMARY The polymer-metal ion interactions were studied by cyclic voltammetry. These were carried out with poly(acrylic acid)-Cu(II) and poly(vinylsulfonic acid)-Cu(II) systems at different pH. At low pH, the polymer was adsorbed on the electrode surface increasing the irreversibility of the Cu2+/Cu(s) redox system. At pH 2.7, it was possible to demonstrate that the interaction between Cu(II) and poly(vinylsulfonic acid) is basically electrostatic and with poly(acrylic acid) a complex formation also exists.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 39 (1997), S. 653-660 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract. The mathematical description of the retention profiles of metal ions by water-soluble polymers using the Liquid-Phase Polymer Based Retention (LPR) technique is discussed for the system poly(acrylic acid)-Ni(II), and poly(acrylic acid)-Co(II). Two experiences have been done under constant and variable conditions. The dissociation constants are calculated from the theoretical expressions of the experimental retention profiles.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: SUMMARY The synthesis of two copolymers of poly[acrylamide-co-(N-(hydroxymethyl)acrylamide)] is described. Polymer analogous reactions have been used as well as direct radical polymerization. The two copolymers have been fractionated and ultrafiltered in the presence of Cu2+, Cd2+, Co2+, Ni2+, Pb2+, Zn2+, and an excess of Na+. It has been found that Na+ ions do not interact with the copolymers. The effect of the different composition of the copolymers is noted in the study of Cu2+ and Pb2+, but there is no difference in the retention profiles obtained for the rest of the metal ions.
    Type of Medium: Electronic Resource
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  • 4
    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 metal-complexing properties of five different polyaziridines - poly[1-(2-aminoethyl)aziridine], poly(1-acetylaziridine), poly[1-(2-hydroxyethyl)aziridine], poly[1-(2-hydroxyethyl)aziridine-co-1-acetylaziridine], and poly[1-(2-aminoethyl)aziridine] oxine - were investigated in an aqueous solution with regard to the side-chain effects using membrane filtration. The results are discussed and compared with the stability constants of metalcomplexation of the corresponding functional moieties. Poly[1-(2-aminoethyl)aziridine], a poly(aziridine) with neutral nitrogen donors in the side chains, showed similar complexing properties to those of ammonia. The only exceptions are Fe(III) and Cr(III), which cannot form complexes with ammonia but can be retained in the membrane filtration process due to the formation of Fe(III)-colloidal species and hydroxides. The complexing properties of polyaziridines containing hydroxyl groups in the side chains (i.e., poly[1-(2-hydroxyethyl)aziridine] and poly[1-(2-hydroxyethyl) aziridine-co-1-acetylaziridine] can be explained and described by the formation constants with the corresponding hydroxides. The introduction of a carbonyl moiety in the polyaziridine side chain, e.g., polyacetylaziridine, reduces the complexing ability for metal ions because the carbonyl group cannot form complexes with the metal ions investigated. Poly[1-(2-aminoethyl)aziridine]oxine showed the strongest complexing ability in the series of metal ions due to the strong complexing ligand 8-hydroxy quinoline attached to the polymer backbone. © 1996 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1436-2449
    Keywords: Keywords: Nucleophilic and electrophilic monomers; spontaneous copolymerization; non-alternating copolymers.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The copolymerization of p-chlorophenylmaleimide (1) as electrophilic monomer with 2-methyl-2-oxazoline (2) as nucleophilic monomer without initiator in solution under different experimental conditions was investigated. Copolymers were characterized by FT-IR and 1H-NMR spectroscopy. The copolymer composition was determined from 1H-NMR spectra. Molecular weights ranged between 1700 and 5400 g/mol by vapor pressure osmometry.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: SUMMARY The crosslinked poly([2-(methacryloyloxy)ethyl]trimethyl ammonium chloride-co-acrylic acid) was tested as adsorbent for Cd(II), Hg(II), Zn(II), Pb(II), Cr(III), and U(VI) by batch equilibrium procedure. At pH 5.0 the adsorbent retained 74% (1.865 meq/g) of U(VI) with a maximum capacity of load of 2.7 meq/g (108 mg/g). The resin-U(VI) equilibrium was achieved around of 1 h which is considered adequate for a heterogeneous reaction. It showed a high selectivity for U(VI) respect to all the other metal ions both from competitive and non-competitive conditions. The recovery of the resin was over 65% by H2SO4 and Na2CO3.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 36 (1996), S. 157-164 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary The cationic polymerization of 2-methylaziridine using boron trifluoride etherate as initiator at different monomer/initiator ratios, temperatures, solvents, and times of polymerization was carried out. The effect of these variables on the polymerization yield and viscosity of the polymers was studied. All the polymers were characterized by elemental analysis, FT-IR, 1H-NMR, 13C-NMR spectroscopy, thermogravimetric analyses and differential scanning calorimetry.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 2665-2672 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization of 1-(2-hydroxyethyl)aziridine (1) as nucleophilic monomer with β-butyrolactone (2) as electrophilic monomer without initiator in solution at 45°C was investigated. Copolymers were characterized by IR and 1H NMR spectroscopy. By elemental analyses it could be shown that their compositions depend on the monomer ratio in the feed. From the copolymer composition and 1H NMR spectra it was possible to suggest four probable copolymer structures.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 149-154 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 2-Ethyl-2-oxazoline (ETOX) as nucleophilic monomer and β-butyrolactone (BUL) as electrophilic monomer were copolymerized in bulk in the absence of initiator at 45°C. Copolymers were characterized by elemental analysis, IR, 1H NMR, and 13C NMR spectroscopy. The copolymer composition was determined by elemental analysis and by 1H NMR spectroscopy. All copolymers contain a BUL:ETOX mole ratio greater than one.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 187 (1986), S. 71-79 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The zwitterionic copolymerization of 2-methyl-2-oxazoline (MOX) as nucleophilic monomer with β-butyrolactone (BUL) as electrophilic monomer was investigated in bulk and in solution (CH3CN) at 45°C. The copolymer composition was around 1,5/1,0 (BUL/MOX) as was established by 1H NMR. 1H and 13C NMR spectroscopy were used to identify the copolymers. The IR spectroscopy supported the NMR results. On the other hand, the copolymers behave as polyelectrolytes, according to viscosity determinations. A copolymerization mechanism through a zwitterion species is suggested.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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