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  • Polymer and Materials Science  (22)
  • NMR relaxation studies  (2)
  • Sulfate reducers  (2)
  • 1
    ISSN: 1432-072X
    Keywords: Archaea ; Methanogens ; Sulfate reducers ; Tetrahydromethanopterin ; Methanofuran ; Coenzyme F420 ; C1-Enzymes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The sulfate-reducing Archaeoglobus fulgidus contains a number of enzymes previously thought to be unique for methanogenic Archaea. The purification and properties of two of these enzymes, of formylmethanofuran: tetrahydromethanopterin formyltransferase and of N 5,N 10-methylenetetrahydromethanopterin dehydrogenase (coenzyme F420 dependent) are described here. A comparison of the N-terminal amino acid sequences and of other molecular properties with those of the respective enzymes from three methanogenic Archaea revealed a high degree of similarity.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-072X
    Keywords: Archaea ; Methanogenic bacteria ; Hyperthermophiles ; Sulfate reducers ; Methanobacterium thermoautotrophicum ; Methanosarcina barkeri ; Tetrahydromethanopterin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Archaeoglobus fulgidus and Methanopyrus kandleri are both extremely thermophilic Archaea with a growth temperature optimum at 83°C and 98°C, respectively. Both Archaea contain an active N 5,N 10-methenyltetrahydromethanopterin cyclohydrolase. The enzyme from M. kandleri has recently been characterized. We describe here the purification and properties of the enzyme from A. fulgidus. The cyclohydrolase from A. fulgidus was purified 180-fold to apparent homogeneity and its properties were compared with those recently published for the cyclohydrolase from M. kandleri. The two cytoplasmic enzymes were found to have very similar molecular and catalytic properties. They differed, however, significantly with respect of the effect of K2HPO4 and of other salts on the activity and the stability. The cyclohydrolase from A. fulgidus required relatively high concentrations of K2HPO4 (1 M) for optimal thermostability at 90°C but did not require salts for activity. Vice versa, the enzyme from M. kandleri was dependent on high K2HPO4 concentrations (1.5 M) for optimal activity but not for thermostability. Thus the activity and structural stability of the two thermophilic enzymes depend in a completely different way on the concentration of inorganic salts. The molecular basis for these differences are discussed.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 10 (1985), S. 391-402 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The azeotropic 80:20 styrene-acrylonitrile mixture was polymerized in 190nm- and 300nm-diameter monodisperse polystyrene seed latexes by batch, batch-with-equilibrium-swelling, and semi-continuous polymerization. Polystyrene seed latexes were used to determine the degree of grafting of the substrate as well as the styrene-acrylonitrile copolymer. The Arrhenius plot of log (polymerization rate) of the seeded batch copolymerizations with reciprocal temperature comprised two linear regions with a sharp inflection point at 65°C. Specific volume measurements showed that the Tg of the monomer-swollen styrene-acrylonitrile copolymer was also 65°C. The final latex comprised the original seed particles grown to a larger size and, in some cases, a new crop of particles formed during the polymerization. The critical factor determining the formation of new particles was the surface area of the seed latex: at or above 226 m2/dl, new particles were not formed; at or below 179 m2/dl, a new crop of particles was nucleated, the number increasing with decreasing surface area. The degree of grafting of the polystyrene seed substrate was greater for the smaller particle size seed latex, and increased exponentially with increasing seed surface area. The amount of grafted styrene-acrylonitrile copolymer determined the stability of the grafted particles in acetone, a good solvent for the copolymer. Dynamic mechanical spectroscopy showed that the continuous phase was either the polystyrene substrate (Tg 104°C) or the styrene-acrylonitrile copolymer phase (Tg 120°C) except where the degree of grafting was high, in which case, the Tg was intermediate between the two values. Electron microscopy of thin film sections stained with ruthenium tetroxide confirmed which phase was continuous and showed interpenetrating networks for those systems of intermediate Tg.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 2117-2131 
    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: Sulfonated polystyrene latex particles were used as acid catalysts in the continuous inversion of sucrose at 50-70°C. The particles (surface charge 168 μeq/g) were confined in a stirred reactor with a semipermeable membrane; sucrose solution was pumped in, and product solution was pumped out. The catalytic activity of the particles was unchanged after 20 days continuous use. Variation of particle size (0.13 and 0.42 μm) and stirring rate showed that internal and external mass transfer was not a controlling factor. The kinetics were pseudo-first-order; the rate constant at 70°C was 2.30/N min as compared with 0.07/N min for macroporous sulfonated ion-exchange resin; the apparent activation energy was 111 kJ/mol as compared with 121 kJ/mol for the homogeneous acid-catalyzed reaction. The faster rate was attributed to the very great surface area, high charge density, and lack of internal diffusional resistance of the latex particles. The proposed mechanism comprised adsorption of sucrose on the particle surface, followed by inversion and desorption of product.
    Additional Material: 12 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 3173-3181 
    ISSN: 0887-624X
    Keywords: macromonomer ; core/shell latexes ; interphase ; compatibilizing agent ; NMR relaxation studies ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this work poly(methyl methacrylate) (PMMA) macromonomer is used as a compatibilizing agent in a poly(butyl acrylate) (PBA)/PMMA core/shell latex system. The incorporation of the PMMA macromonomer was achieved by copolymerizing it with BA monomer using miniemulsion polymerization. PBA seed latex was also synthesized without the macromonomer present to compare the compatibilizing effects with the PMMA macromonomer. The second stage methyl methacrylate monomer was added semi-continuously to the PBA seed latexes under monomer-starved conditions. Solid-state 13C-NMR [H]T1ρ relaxation studies were used to determine the effect of PMMA compatibilizer on these PBA/PMMA core/shell latex interphase regions. The thickness of the interphase of the core/shell particles prepared with and without the PMMA macromonomer compatibilizing agent are calculated to be in the range of 15-16 nm and 10-12 nm, respectively. Electron microscopy revealed that the seed latex prepared with the PMMA macromonomer achieved a more uniform coverage with the second stage PMMA polymer as compared to the latex synthesized without the compatibilizing agent present. It is concluded that the PMMA macromonomer is effective in increasing the thickness of the interphase region and also the amount of interfacial PMMA. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 3183-3190 
    ISSN: 0887-624X
    Keywords: macromonomer ; core/shell latexes ; interphase ; compatibilizing agent ; NMR relaxation studies ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this work poly(methyl methacrylate) (PMMA) macromonomer is used as a compatibilizing agent in a poly(butyl acrylate) (PBA)/PMMA core/shell latex system. The incorporation of the PMMA macromonomer was achieved by copolymerizing it with BA monomer using miniemulsion polymerization. PBA seed latex was also synthesized without the macromonomer present to compare the compatibilizing effects with the PMMA macromonomer. The second stage methyl methacrylate monomer was added semi-continuously to the PBA seed latexes under monomer-starved conditions. Solid-state 13C-NMR [H]T1ρ relaxation studies were used to determine the effect of PMMA compatibilizer on these PBA/PMMA core/shell latex interphase regions. The thickness of the interphase of the core/shell particles prepared with and without the PMMA macromonomer compatibilizing agent are calculated to be in the range of 15-16 nm and 10-12 nm, respectively. Electron microscopy revealed that the seed latex prepared with the PMMA macromonomer achieved a more uniform coverage with the second stage PMMA polymer as compared to the latex synthesized without the compatibilizing agent present. It is concluded that the PMMA macromonomer is effective in increasing the thickness of the interphase region and also the amount of interfacial PMMA. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 461-473 
    ISSN: 0887-624X
    Keywords: calorimetry ; styrene ; kinetics ; emulsion polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An automated reaction calorimeter was used to directly monitor the rate of emulsion polymerization of styrene using different emulsifier (sodium lauryl sulfate) and initiator (potassium persulfate) concentrations. By using this technique in conjunction with off-line measurements of the evolution of the particle size distributions, important details of the process were observed. The classical constant rate period (Interval II) often reported for the batch emulsion polymerization of styrene was not seen in this work. Instead, the experimental results suggest that the end of nucleation and the disappearance of monomer droplets take place at approximately the same conversion (36-40%). From the polymerization rate data, important parameters such as the monomer concentration in the polymer particles and the average number of radicals per particle were calculated. © 1996 John Wiley & Sons, Inc.
    Additional Material: 15 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3813-3825 
    ISSN: 0887-624X
    Keywords: reaction calorimetry ; emulsion polymerization ; kinetics ; styrene ; nonionic surfactant ; Triton X-405 ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The emulsion polymerization of styrene was studied using the nonionic surfactant Triton X-405 (octylphenoxy polyethoxy ethanol). Two separate nucleation periods were noted in these polymerizations resulting in bimodal final latex particle size distributions. The partitioning of the surfactant between the phases was found to play the major role in determining the nucleation mechanism(s) in these polymerizations. Although the total concentration of the emulsifier was always added at a level above its critical micelle concentration (CMC) based on the water phase in the recipe, it was found that the portion of the surfactant initially present in the aqueous phase was below its CMC due to the partitioning. This CMC was also found to increase with increasing total surfactant because the distribution of the surfactant (varying ethylene oxide chain length) depended on the partitioning between the phases. Under these conditions, the first of the two nucleation periods was attributed to homogeneous nucleation, while the second was attributed to micellar nucleation. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3813-3825, 1997
    Additional Material: 15 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3827-3835 
    ISSN: 0887-624X
    Keywords: reaction calorimetry ; emulsion polymerization ; n-butyl acrylate ; nonionic surfactant ; Triton X-405 ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In the emulsion polymerization of n-butyl acrylate, the nonionic surfactant Triton X-405 (octylphenoxy polyethoxy ethanol) partitions primarily into the aqueous phase leading to nucleation in the presence of micelles and unimodal final latex particle size distributions. Nucleation is accompanied by limited aggregation in the early stages of the reactions with particles being formed in some cases past 50% conversion depending on the experimental conditions. High values of the average number of radicals per particle (n̄ 〉 10) are observed during these reactions which explains a secondary increase in the heat of reaction. This increase was not observed when the initiator (K2S2O8) concentration was reduced from 6.4 to 0.6 mM or the temperature was decreased from 70°C to 60°C; contrary to what was expected, an inverse relationship was observed between the rate of polymerization and the final number of particles for these experiments. This was attributed to more extensive limited aggregation at the higher temperature and initiator concentration. Limited aggregation is thus shown to be an important mechanism in these polymerizations. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3827-3835, 1997
    Additional Material: 11 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 3837-3846 
    ISSN: 0887-624X
    Keywords: reaction calorimetry ; emulsion copolymerization ; styrene ; n-butyl acrylate ; nonionic surfactant ; Triton X-405 ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Emulsion copolymerizations of styrene and n-butyl acrylate were conducted at 70°C using varying amounts of Triton X-405 (octyl phenoxy polyethoxyethanol) as emulsifier. The kinetic behavior was found to vary widely depending on the emulsifier concentration. Unimodal particle size distributions were produced at the lowest (4.2 mM) and the highest levels (12.5 mM, 16.2 mM) of emulsifier while at intermediate levels (6.3 mM and 8.4 mM) bimodal distributions were produced; these were reflected in the reaction kinetics. These results were attributed to the surfactant partitioning behavior in the system which led to homogeneous/coagulative nucleation at the lowest level to homogeneous/coagulative nucleation followed by micellar nucleation at the intermediate levels to micellar nucleation at the highest levels. Although the added surfactant levels were all well above that required to exceed its CMC in the aqueous phase, the substantial partitioning into the oil phase lead to conditions well below the CMC of the portion of the surfactant present in the aqueous phase for the lowest and the intermediate levels of the Triton X-405. Consequences of this partitioning were seen in a semibatch reaction where all the surfactant was initially present in the aqueous phase; in this case, too many particle were nucleated leading to massive coagulation due to insufficient surfactant being available to stabilize the particles. © John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3837-3846, 1997
    Additional Material: 10 Ill.
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