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  • 11
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 32 (1976), S. 1900-1903 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 43 (1987), S. 912-914 
    ISSN: 1420-9071
    Keywords: Br-MRBC ; monoclonal antibodies ; autoimmunity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Autoantibodies reacting with bromelain-treated autologous mouse red blood cells (Br-MRBC) are spontaneously produced by normal mice. In order to understand the biological significance of these autoantibodies, anti-Br-MRBC monoclonal autoantibodies have been prepared and studied for reactivity with a panel of frozen tissue sections from organs of normal mice by direct immunofluorescence. It has been found that the anti-Br-MRBC monoclonal autoantibodies are polyspecific, since they react with cells in multiple organs.
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  • 13
    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 Fast atom bombardment mass spectrometry (FAB-MS) has been used to identify oligomers with different end groups obtained by the carbonate interchange reaction of bisphenol-A with dimethyl carbonate and the partial methanolysis of poly(bisphenol-A carbonate)s. Based on the FAB-MS data, a reaction pathway for the formation of compounds in the synthesized oligomers is proposed.
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  • 14
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1653-1662 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: MS and GPC analyses are used to identify the cyclic oligomers formed in the polycondensation reactions of aromatic dithiols and dibromoalkanes leading to aromatic-aliphatic polysulfides. A correlation exists between the two sets of data obtained by these techniques. Mass spectra of the cyclic oligomers formed in the polymerization reactions are reported.
    Additional Material: 7 Ill.
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  • 15
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 1873-1884 
    ISSN: 0887-624X
    Keywords: polycarbonate ; poly(methyl methacrylate) ; blends ; exchange reactions ; mass spectrometry ; thermal degradation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical reactions occurring in the thermal treatment of bisphenol-A polycarbonate (PC) and poly(methyl methacrylate) (PMMA) blends have been investigated by nuclear magnetic resonance (NMR), mass spectrometry (MS), size exclusion chromatography (SEC), and thermogravimetry (TG). Our results suggest that in the melt-mixing of PC/PMMA blends, at 230°C, no exchange reactions occur and that only the depolymerization reaction of PMMA has been observed. In the presence of an ester-exchange catalyst (SnOBu2), an exchange reaction was found to occur at 230°C, but no trace of PC/PMMA graft copolymer has been observed. Instead, an exchange reaction between the monomer methyl methacrylate (MMA), generated in the unzipping of PMMA chains, and the carbonate groups of PC has been suggested. This is due to the diffusion of MMA at the interface or even into the PC domains, where it can react with PC producing low molar mass PC oligomers bearing methacrylate and methyl carbonate chain ends and leaving the undecomposed PMMA chains unaffected. The TG curves of PC/PMMA blends prepared by mechanical mixing and by casting from THF show two separated degradation steps corresponding to that of homopolymers. This behavior is different from that of a transparent film of PC/PMMA blend, obtained by solvent casting from DCB/CHCl3, which shows a single degradation step indicating that the degradation rate of PC is increased by the presence of PMMA in the blend. The thermal degradation products obtained by DPMS of this blend consist of methyl methacrylate (MMA), cyclic carbonates arising from the degradation of PMMA and PC, respectively, and a series of open chain bisphenol-A carbonate oligomers with methacrylate and methyl carbonate terminal groups. The presence of the latter compounds suggests a thermally activated exchange reaction occurring above 300°C between MMA and PC. The presence of bisphenol-A carbonate oligomers bearing methyl ether end groups, generated by a thermally activated decarboxylation of the methyl carbonate end groups of PC, has also been observed among the pyrolysis products. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1873-1884, 1998
    Additional Material: 8 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 475-487 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal degradation of four aliphatic polysulfides (polythiomethylene, polythiotrimethylene, polythioethylene, and polythiohexamethylene) was investigated by direct pyrolysis in the ion soruce of a mass spectrometer (DPMS) operating both in electron impact (E.I.) and chemical ionization (C. I.) modes. Flash-pyrolysis GCMS was also used in the case of polythiomethylene(polysulfide I) to confirm the DPMS results. The overall evidence indicates that the primary thermal decomposition of these polymers yields cyclic sulfides by an intramolecular exchange process. A β-CH hydrogen transfer reaction, occurring in parallel with the former process, produces primary pyrolysis compounds with SH end-groups.
    Additional Material: 6 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 31 (1986), S. 1269-1274 
    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: Thermal stability and flammability properties of six structurally related vinyl and vinylidene polymers fail to show correlation. Instead, it is found that the combustion of these polymers is dominated by their char-forming ability. A remarkable intumescent effect is observed in PVC2, PVF2, and PVC which accounts for the high flame extinguence of these polymers.
    Additional Material: 3 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Numerical Linear Algebra with Applications 3 (1996), S. 275-300 
    ISSN: 1070-5325
    Keywords: sparse QR factorization ; multifrontal method ; parallelism ; Engineering ; Engineering General
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mathematics
    Notes: We describe the design and implementation of a parallel QR decomposition algorithm for a large sparse matrix A. The algorithm is based on the multifrontal approach and makes use of Householder transformations. The tasks are distributed among processors according to an assembly tree which is built from the symbolic factorization of the matrix ATA.We first address uniprocessor issues and then discuss the multiprocessor implementation of the method. We consider the parallelization of both the factorization phase and the solve phase. We use relaxation of the sparsity structure of both the original matrix and the frontal matrices to improve the performance. We show that, in this case, the use of Level 3 BLAS can lead to very significant gains in performance. We use the eight processor Alliant˜FX/80 at CERFACS to illustrate our discussion.
    Additional Material: 12 Ill.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 1743-1750 
    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 influence of ammonium polyphosphate (APP) and hexabromocyclododecane (HBCD) as flame retardant (FR) on poly(acrylonitrile) (PAN) has been examined. The APP-HBCD system behaves as an intumescent flame retardant (IFR) formulation, APP being the char-forming agent and HBCD the blowing agent. A negligible gas-phase mode of action was ascertained for HBCD with this substrate. A synergism between the two FR agents was observed, corresponding to about 50% increased efficacy with respect to the separate effects of the two components. Thermogravimetry (TG), oxygen index (OI), nitrous oxide index (NOI) experiments and phosphorous residue measurements were performed to substantiate the conclusion that a conclusion that a condensed phase mechanism of action accounts for all the facts observed.
    Additional Material: 5 Ill.
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 1449-1460 
    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 action of some mixtures of ammonium polyphosphate (APP) and polyurethanes (PUr) as flame retardant (FR) agents for polypropylene (PP) was examined. The APP-PUr systems behave as intumescent flame retardant (IFR) formulations. The IFR action of these systems is described by the comparison of the oxygen index (OI) values measured on molded pellets and on molded rods, by measurements of the polymer temperature just below the burning surface and by visual observations. A strong synergism between APP and some polyurethanes, having piperazine units in the polymer chain, was ascertained with a maximum 3:1 ratio. Our results also indicate that only polyurethanes with specific structure, in combination with APP, are active as IFR agents on PP combustion.
    Additional Material: 6 Ill.
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