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  • 1
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Analytica Chimica Acta 281 (1993), S. 111-118 
    ISSN: 0003-2670
    Schlagwort(e): Amines ; Chemiluminescence ; Fish ; Flow injection ; Foods ; Histamine
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Analytica Chimica Acta 287 (1994), S. 83-88 
    ISSN: 0003-2670
    Schlagwort(e): Chemiluminescence ; Liquid chromatography ; Plants ; Polyamines ; Tomatoes
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 58 (1995), S. 2451-2458 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: 2-Dibutylamino-1,3,5-triazine-4,6-dithiol (DB) and a mixture of DB and triallylisocyanurate (TAIC) were used as a lubricant during steel wire drawing due to a dry process. DB gave a polymer film with 180 nm in thickness to wire surfaces during the wire drawing. The polymer film had a disulfide structure on the backbone and contained a small amount of DB monomer and olygomer. Molecular weight and polymer weight increased with the drawing rate. The mixture of DB and TAIC gave mainly a three-dimensional polymer film with 225 nm in thickness to wire surfaces during drawing. The polymer film insoluble in THF had mono and disulfide structures and contained a small amount of linear polymer, DB, and TAIC. Such tribological polymerizations are estimated as follows: DB produces dithiyl radicals on a nascent surface formed during drawing and in the presence of oxygen and heat. The dithiyl radicals were polymerized by coupling with each other to give disulfide bonds or added to allyl groups in TAIC to give monosulfide bonds. It is concluded that this technique should be possible to use for unifying metal processing and surface treatment. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 1077-1091 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The changes in temperature and crystallinity of polymer during nonisothermal crystallization were theoretically analyzed assuming a cooling condition under which heat transfer occurs at a rate proportional to the difference in temperature between polymer and the environment. When a plateau appears in the temperature change during crystallization, crystallization temperature can be predicted by a simple method. This method gives nearly the same value as that obtained by successive calculations of temperature and crystallinity throughout the whole process. In addition, a graphic method is presented to predict crystallization temperature. By using the plateau temperature observed in melt-spinning experiments, the crystallization rate under molecular orientation is evaluated. Furthermore, a method applicable to estimating the ultimate crystallinity is proposed. A rough estimation of the increase in the rate of crystallization under molecular orientation was carried out for very high-speed spinning of poly(ethylene terephthalate).
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 2465-2470 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The absorption isotherms of methanesulfonic acid, ethanedisulfonic acid, and R-acid on nylon fiber were determined in water and ethylene glycol at 80°C. The saturation values of the sulfonic acids on the nylon fiber were determined by extrapolation of a reciprocal plot of the absorption isotherms. In water, the saturation values of the three acids were near the amino group content of the fiber. In ethylene glycol, the saturation values of the dibasic acids, ethanedisulfonic acid and R-acid, were much larger than the stoichiometric quantity corresponding to the amino group content of the nylon fiber, approximately twice, though the saturation value of the monobasic acid, methanesulfonic acid, was near the amino group content. A dyeing model of nylon with polybasic dyes was proposed, in order to explain how a polybasic dye can physically saturate fixed sites.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Alternating polyamide esters of structures A and B were obtained by melt polymerization of dimethyl adipate and terephthalate or by solution polymerization of adipoyl and terephthaloyl chlorides, with N,N′-di(6-hydroxycaproyl)diamines and an N-6-hydroxycaproyl aminoalcohol: \documentclass{article}\pagestyle{empty}\begin{document}$ \begin{array}{*{20}c} {\rlap{--} [{\rm O(CH}_2 )_5 {\rm CONHR}_{\rm 1} {\rm NHCO(CH}_{\rm 2} {\rm )}_{\rm 5} {\rm OCOR}_{\rm 2} {\rm CO}\rlap{--} ]_n } \\ {\mathop {{\rm \rlap{--} [O(CH}_{\rm 2} {\rm )}_{\rm 5} {\rm CONHR}_{\rm 1} {\rm OCOR}_{\rm 2} {\rm CO\rlap{--} ]}_{\rm 2} }\limits_{\rm B}^{\rm A} } \\ \end{array} $\end{document} where R1 is selected from dimethylene, hexamethylene, and p-phenylene radicals, and R2 is selected from tetramethylene or p-phenyl radical. Polyamide esters of structure A′ were also prepared: Average values of melting points of the resulting polyamide esters were dependent on the starting diacid derivatives, amide diols, and methods of polymerizations as follows: \documentclass{article}\pagestyle{empty}\begin{document}$ \begin{array}{l} {\rm CPZ 〈 ECA 〈 CHD 〈 CED 〈 CPPD} \\ {\rm DMA 〈 ADC 〈 DMT 〈 TPC} \\ {\rm melt polymerization 〈 solution polymerization} \\ \end{array} $\end{document} where CPZ, CHD, CED, and CPPD are N,N′-di(6-hydroxycaproy1)-, each in this order: piperazine, hexamethylenediamine, ethylenediamine, and p-phenylenediamine. ECA is N-(2-hydroxyethyl)6-hydroxycaproamide. For a given polyamide ester obtained from the same starting materials and by the same method of polymerization, the melting points increased with inherent viscosities. Polyamide esters of high molecular weight were obtained from CHD with both adipic and terepbthalic derivatives both by melt and solution polymerizations. Polymerizations of the other amide diols gave lower molecular weights. Solution polymerization gave colorless or light-colored polymers, while melt polymerization gave deeper-colored polymers.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 369-377 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Cooligomers and ABA-type block copolymers composed of a hydrophilic monomer, 2-hydroxyethyl methacrylate (HEMA), and a hydrophobic monomer, styrene, were synthesized to study the relation between their microstructure and hydrophilic and hydrophobic functions. Films of cooligomers and ABA-type block copolymers were cast from DMF solutions at 40°C. The wettability, which was determined from the contact angle with water, increased considerably when HEMA mole fraction reached around 0.8 in the cooligomer system and around 0.9 in the ABA-type block copolymer system. The microstructures of the copolymer films were observed by electron microscopy using the osmium tetroxide fixation technique. The morphologic change in the domain structure was observed at an HEMA mole fraction of about 0.8 in the cooligomer system and about 0.9 in the ABA-type block copolymer system. It is suggested that hydrophilic and hydrophobic functions are largely influenced by the state of aggregation of each segment, that is, the size and geometry of the hydrophilic and hydrophobic domains.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Polyamideurethans of structures I and II were prepared by reacting N,N′-di-(6-hydroxycaproyl)alkylenediamines and N-hydroxyalkyl-6-hydroxycaproamide with hexa-methylene diisocyanate and 4,4′-diphenylmethane diisocyanate: where R1 is either a dimethylene or hexamethylene radical, and R2 is a hexamethylene or 4,4′-diphenylmethane radical. Polymers I and II were of a high degree of polymerization and crystallinity, had high enough melting points for practical use, and gave colorless tough films both by dry and melt castings. The polymers from hexamethylene diisocyanate were much more crystalline and thermally more stable above the melting points than those from 4,4′-diphenylmethane diisocyanate. Polymerization conditions and characteristic properties of the resulting polymers were studied.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 1031-1041 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: In the previous paper a practical method has been applied for an analysis of non-isothermal crystallization in terms of data of isothermal crystallization. The fundamental equation was written on the assumption of the isokinetic conditions in the following form: \documentclass{article}\pagestyle{empty}\begin{document}$ X\left( {\rm t} \right) = 1 - \exp \left[ { - \left( {\int_0^t {K\left( T \right)d\tau } } \right)^n } \right] $\end{document} where X(t) is the degree of phase transformation at time t, and n is the Avrami index determined in the isothermal experiments; K(T) is connected with the crystallization rate constant of the isothermal crystallization, k(T), through the relation K(T) = k(T)1/n. The equation is derived on the basis of the well-known theory of phase transformation. Experiments of nonisothermal crystallization of high-density polyethylene were carried out under various cooling conditions. The change in crystallinity during the process was followed by using the above equation in the course of the primary crystallization. A procedure of the analysis of the whole, including both the primary and secondary processes, is suggested as an eminently practical one on a more general assumption.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 615-623 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Crystallization during melt spinning is studied as an example of the nonisothermal crystallization of polymers. The following equation is derived, taking the temperature distribution within a filament into consideration: \documentclass{article}\pagestyle{empty}\begin{document}$$ \kappa \nabla ^2 T = {\rm V} \cdot {\rm grad } \ T - \frac{{\Delta H}}{{C_p }}{\rm V} \cdot {\rm grad } \ X $$\end{document} where T = temperature, X = crystallinity, κ = thermal diffusivity, V = velocity, ΔH = heat of crystallization, and Cp = specific heat at constant pressure. The assumptions and the procedure for a numerical calculation of crystallinity and temperature within a running filament are described, and some results of calculation are illustrated. The results are compared with those obtained by a simpler calculation in which the radial temperature distribution is neglected. The simpler method proved useful in connection with x-ray measurements.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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