Library

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
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 3080-3087 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 6332-6340 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 26 (1993), S. 60-64 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 5993-5999 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 187 (1986), S. 899-911 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Carbon-13 NMR was used to investigate the structure of a cellulose derivative, ethyl-O-(hydroxyethyl)cellulose (EHEC). Analysis of high molecular weight samples in solution showed that the line widths of the main chain carbon resonances are very sensitive to the concentration of the solution. Above a certain concentration, excessive broadening occurs due to gel formation, which makes a quantitative evaluation of the degree of substitution difficult. If the concentration is decreased below the critical value for gel formation, the use of NMR parameters suitable for quantitative measurements (no NOE and long pulse intervals) leads to excessively long accumulation times. Spectra of solid samples obtained by cross-polarization magic angle spinning (CP-MAS) NMR exhibit better defined resonances of the main-chain carbons than do the spectra of solutions with concentrations above the critical value for gel formation. Variable contact time experiments with a specific sample indicated that a suitable contact time should be 400 μs. The quantitative evaluation of the total degree of substitution by CP-MAS NMR yielded values in agreement with those obtained by GC-analysis.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 188 (1987), S. 513-525 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The substitution pattern of ethyl O-hydroxyethyl cellulose (EHEC) was studied using 13C NMR spectroscopy on the hydrolysates. The hydrolysates of hydroxyethyl cellulose (HEC) and ethyl cellulose (EC) were investigated as well. The high mobility in the hydrolysates gives a much better resolution than that of the corresponding polymer solutions. Beside the determination of the total degree of substitution, the specific substitution at O2 and O3 can be determined. In highly substituted samples it is also possible to directly determine the fraction of unsubstituted O6-positions. However, the latter can be obtained for all samples by combining the NMR results of O2 and O3 substitution with the HPLC analysis of unsubstituted glucose, units. The effect of the substitution pattern on the resistance against enzymatic degradation was also investigated. The reducing-end residues formed by enzymatic attack on EHEC are shown to be unsubstituted at O2. A qualitative comparison between the number of degradable positions according to earlier published results on HEC and changes in molecular weight shows a good correlation.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 191 (1990), S. 2663-2673 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ziegler-Natta catalysts supported on MgCl2 have been studied by CP-MAS (cross-polarization, magic-angle spinning) 13C NMR spectroscopy. The support was activated mechanically and chemically, and then treated with a monoester (ethyl benzoate) or a diester (diisobutyl phthalate). Catalytic species were obtained by a treatment with TiCl4. Complexation and crystal disordering phenomena are clearly observed as changes in the chemical shifts and line broadenings. Line splittings were observed, especially for the diester due to nonequivalent crystal coordination sites. The diester shows a different behaviour compared to the monoester thus reflecting its better ability as a stereoselectivity-controlling agent. The titanation led to the formation of a new, estercontaining and ordered complex on the surface of the carrier. The mobility of the surface complexes is restricted, crystalline complexes being more constrained.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 129-140 
    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 effect of diffusion control on the polymerization of vinyl chloride has been studied by observing the rate as well as the molecular weight and the thermal stability of the polymer formed. The polymerizations were performed at 97% of saturation pressure in a water-suspended system at 55°C, using emulsion PVC latex as seed and a water-soluble initiator. The monomer was charged as vapor from a storage vessel kept at a lower temperature. Characterization included determination of molecular weight distribution by GPC and viscometry, and thermal dehydrochlorination. The gas-liquid contact was varied by changing the speed of agitation and the design of the stirrer. With a propeller the polymerization rate increased with the agitation up to ca. 1000 rpm, where after it became almost constant. Simultaneously, the molecular weight and the thermal stability increased. This indicates diffusion control, and thus decreased monomer concentration, at low agitation speeds, while the polymerization becomes reaction controlled at higher speeds. By a comparison with earlier data, obtained at different pressures and under reaction control, the actual monomer concentration could be calculated, which allowed an evaluation of the mass transfer constant. The possibilities to encounter problems with diffusion control in commercial polymerization of vinyl chloride is discussed. It is demonstrated that diffusion control is utilized in continuous polymerization of vinyl chloride, which explains the lower thermal stability of such materials.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 24 (1986), S. 1313-1335 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl chloride was polymerized at 53-97% of the saturation pressure in a water-suspended system at 55°C with an emulsion PVC latex as seed. A water-soluble initiator was used in various concentrations. The monomer was continuously charged as vapor from a storage vessel kept at lower temperature. Characterization included determination of molecular weight distribution and degree of long-chain branching by gel chromatography and viscometry and by thermal dehydrochlorination. To avoid diffusion control intense agitation was necessary. At a certain conversion, aggregation of primary particles resulted in restricted polymerization rate. Before aggregation, formation of new particles did not occur as the number of particles was high enough to ensure capture of all oligoradicals. The kinetic equation accepted for ordinary emulsion polymerization of vinyl chloride was qualitatively found to be valid after the pressure drop as well. Decreased termination rate may result in increased polymerization rate at reduced monomer concentration, i.e., a gel effect, especially at low particle numbers and high polymer contents. The molecular weight decreased with decreasing monomer concentration. This is in accordance with the new mechanism suggested for chain transfer to monomer starting with occasional head-to-head additions.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    ISSN: 0935-9648
    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
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...