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  • 1
    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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  • 2
    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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  • 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 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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  • 4
    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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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1153-1160 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The metal-complexing properties of intermolecular complexes of poly(acrylic acid) with poly(acrylamide), and poly(acrylic acid) with poly(N,N-dimethylacrylamide) were studied by means of the liquid-phase polymer based retention (LPR) technique. The metal ion retention ability at pH 5 for 400 μg of Cu(II), Cd(II), Co(II), Cr(III), Hg(II), Ni(II), Pb(II), and Zn(II) was investigated due to their environmental and analytical interest in the presence of 1.1 M of carboxylic acid units and variable amounts of amide groups. The retention profiles of the intermolecular complexes were compared with those of the correspondent homopolymers and copolymers. The retention capacity of poly(acrylic acid) is 100% for all metal ions except for Co(II), Ni(II), and Zn(II) whose values were about 90%, while poly(acrylamide) does not retain any of the metal ion studied. The presence of poly(acrylamide) decreases the retention capacity down to 60% for Co(II) and Ni(II) and to 70% for Zn(II). The decrease on the retention values is dependent on the polymer ratio. A smaller effect is observed by the addition of poly(N,N-dimethylacrylamide) which also decreases the retention capacity down to 80% for Co(II) and Ni(II) for a ratio poly(acrylic acid)/poly(N,N-dimethylacrylamide) = 1/2. The metal ion binding behavior of the interpolymer complexes is very close to that of the copolymers.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 503-508 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel method for the preparation of water-soluble polypyrrole graft copolymers with polyamines or polyimines is described. The polyreaction is performed in acidic solution by using chemical oxidants, e.g. iron(III) chloride or ammonium peroxodisulfate. The graft copolymers showed electrical semiconductivity in the undoped state which can be placed between the high conductivity of polypyrrole and the nonconductivity of the polyimine. Their thermal stability at 250°C is improved compared to polypyrrole. The novel graft copolymers are soluble in water over a wide pH range and have a good processability.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 2293-2299 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization of 1,2,3,6-tetrahydrophthalic anhydride (THPhA) as electrophilic monomer and N-(2-hydroxyethyl)ethyleneimineSystematic name: N-(2-hydroxyethyl)aziridine. as nucleophilic monomer in acetonitrile without initiator was investigated. The copolymers show low incorporation of THPhA in the main chain and preferential incorporation in the side chain by esterification reaction of the hydroxymethyl group. On the basis of the spectroscopic data a copolymer structure is proposed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 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: 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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