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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 533-549 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Experimental studies on the solid-state polymerization (SSP) of polyethylene terephthalate (PET) for the particle sizes of 14-16 mesh at 170-200°C and for the particle sizes of 14-18 mesh at 210-240°C are carried out under a vacuum of about 60 mtorr. Analysis of the data of the concentrations of hydroxyl and carboxyl groups and the number average molecular weight during the SSP allows determinations of the rates of esterification and ester interchange separately. It is found that at the temperature 170-200°C and the particle size 80-100 mesh the SSP is end-group diffusion limiting, and that at the temperature 210-240°C and the particle size 14-16 mesh the ester interchange is ethylene glycol diffusion limiting and the esterification is predominantely end-group diffusion limiting due to higher diffusion rate of water. These phenomena are explored by an assistance of the proposed rate expressions for the end-group diffusion limited reactions and diffusion models for the by-products, water, and ethylene glycol.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of poly(N-methyl-L-alanine) and poly (N-methyl-DL-alanine) are described. The polymers were examined by 220 MHz high-resolution nuclear magnetic resonance (nmr) and circular dichroism (CD). The results demonstrate that poly(N-methyl-L-alanine) exists as an ordered helical structure with all the amide bonds in the trans configuration in appropriate solvents. As trifluoroacetic acid (TFA) is added to the solutions of the polymer in helix-supporting solvents, resonances corresponding to both trans and cis amide conformations of N-methyl, C-methyl, and α-CH are observed. The presence of both the trans and the cis peptide bonds in a polymer chain disrupts the ordered structures. Our conclusions from CD data are in agreement with the nmr results. Ultracentrifugation shows that degradation of the polymer chain does not occur during the TFA treatment.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1213-1223 
    ISSN: 0887-6266
    Keywords: viscoelastic properties ; dynamic light scattering ; dilute nematic solutions ; cyclic liquid crystal polymer ; hyperbranched liquid crystal polymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The twist and bend viscosities of dilute solutions of cyclic and hyperbranched liquid crystal polymers (LCP) dissolved in low molar mass nematic solvents were determined via dynamic light scattering analysis. These results were compared to those of linear chains with similar chemical repeat structures. The nematic solvent used was 4′-pentyloxy-4-cyanobiphenyl (50CB). The cyclic LCP oligomers, Cy TPB10, have a mesogenic group, 1-(4-hydroxy-4′-biphenyl)-2-(4-hydroxyphenyl) butane, separated by flexible decamethylene spacers. The twist viscosity of the cyclic Cy-TPB10 oligomers increases with molecular weight more strongly than the linear, TPB-10, suggesting that the hydrodynamic behavior of Cy-TPB10 is closer to that of a rigid rod than TPB10. Surprisingly, the intrinsic bend viscosity [ηbend] of Cy-TPB10 decreases with molecular weight, in contrast to the positive dependence for linear TPB10. This may reflect the higher strain energy in the smaller ring sizes. The hyperbranched LCP, TPD-b-8, is also based on the mesogen 10-bromo-1-(4-hydroxy-4′-biphenyl)-2(4-hydroxyphenyl) decane but with octyl groups at the chain ends. We compare the viscoelastic behavior of dilute nematic solutions of TPD-b-8 in 50CB against that of a linear main-chain LCP, TPB7, with the same mesogenic group but with heptamethylene spacers. The viscometric properties of TPD-b-8/50CB and TPB7/50CB are quite different. The results suggest that each chain is prolate (i. e., R∥ 〉 R⊥) but that TPD-b-8 has a smaller chain anisotropy than that of TPB7. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 19 (1998), S. 2639-2644 
    ISSN: 0173-0835
    Keywords: Erythropoietin ; Fetuin ; Kallikrein ; Ribonuclease B ; 8-Amino-1,3,6-trisulfonic acid ; Sialidase ; Capillary electrophoresis ; Laser-induced fluoresence detection ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A method for analysis of N-linked oligosaccharides derived from glycoproteins including sialic acid-containing species is presented. It is based on the combination of specific chemical and enzymatic conversions coupled with capillary electrophoretic (CE) separation and laser-induced fluorescence (LIF) detection. Glycoproteins were heat-denatured in the presence of a reducing agent and the N-linked oligosaccharides were released by peptide N-glycosidase (PNGase F; EC3.5.1.52)-catalyzed hydrolysis. The released N-linked oligosaccharides were derivatized with 8-aminopyrene-1,3,6-trisulfonate (APTS) under mild reductive amination conditions in which desialylation and loss of fucose residues are minimized. A model N-linked oligosaccharide, desialylated, galactosylated biantennary, core-substituted with fucose (A2F) was tested for APTS-based derivatization chemistry with excellent recovery of the adduct without losing fucose and neuraminic acid residues. The profiles of heavily sialylated N-linked oligosaccharides derived from fetuin, recombinant human erythropoietin and kallikrein are reported and the data show that the present method produces a high resoluton of the N-linked oligosaccharide profile for fingerprinting glycans derived from glycoproteins.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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