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  • Chemistry  (14)
  • 1995-1999  (7)
  • 1960-1964  (4)
  • 1925-1929  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Potential of adhesives for the future (1962)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. 198-203 
    Details
    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: Rapid technological advancements have contributed to the increasing application of adhesives. Because of these accomplishments, because of continuing materials research and process development activities, and because of their inherent advantages, adhesives have a great potential for the future. Requirements for the future impose a severe challenge on developmental capabilities. More severe structural requirements and environmental conditions may be expected. Because of increasing complexity and costs, there are requirements for significantly higher orders of reliability and lower fabrication costs. Improvements in bonding processes and development of comparatively new techniques are desirable. Test methods require further development and standardization - especially nondestructive methods. Continuing work in collecting and reporting pertinent information, especially on properties and design parameters for adhesive bonding is helping to advance the utilization of adhesives. Current trends indicate that adhesives are progressing from the realm of “art” to science, a factor which should substantially aid in advancing the future potential for adhesives.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1962.070062013
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  • 2
    Electronic Resource
    Electronic Resource
    The Importance of Magnetic Coupling Through Atoms with Large Spin Densities - Structure and Magnetic Properties of meso-Tetrakis-(4′-tert-Butylphenyl)Porphinatomanganese(III) Hexacyanobutadienide, [MnIIITtBuPP]+[C4(CN)6].- (1997)
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 138-142 
    Details
    ISSN: 0947-6539
    Keywords: electron transfer ; magnetic properties ; metalloporphryins ; polymers ; spin density ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [MnIIITtBuPP]+[C4(CN)6].- · 5PhMe [MnIIITtBuPP = meso-tetrakis-(4′-tert-butylphenyl)porphinatomanganese(III)] has been prepared and structurally and magnetically characterized. The uniform, linear-chain (1-D) coordination polymer comprises alternating cations and anions. The bond lengths in planar ion [C4(CN)6].-]'- are 1.377(10) (CC-CC), 1.418(7) (C-CCC), 1.414 (C-CN), 1.457 (C-CNMn), 1.150 (C≡N), and 1.134 Å (C = NMn). The Mn-N-C angle is 172.3(4)°, and the intrachain Mn  -  Mn separation is 10.685 Å. Each [C4(CN)6].-]' unit is bonded to two MnIII atoms through the interior nitrogen atoms in a trans-μ2-N-σ manner with N-Mn bond lengths of 2.353 Å. The ṽCN absorptions are at 2217 (w, br) and 2190 (m) cm-1. Above 50 K the magnetic susceptibility of [MnIIITtBuPP]+[C4(CN)6].- can be fitted to the Curie-Weiss expression, χ∝1(T - θ), with an effective θ of -13 K. This is consistent with weak antiferromagnetic coupling, which is in contrast to the effective θ of +67 K for the uniform chain [MnIIIOEP]+[C4(CN)6].- [OEP = octaethylporphinato]. Here, the [C4(CN)6].-'- units are bonded to the MnIII centers through endo CN nitrogen atoms in a similar trans-μ2 manner. Density functional theory MO calculations reveal that the spin density of the CN nitrogen atom bound to [MnIIITtBuPP]+ (0.019 μBÅ-3) is significantly lower than that of the N atom bound to [MnIIIOEP]+ (0.102 μBÅ-3). This is consistent with the reduced spin coupling observed for [MnIIITtBuPP]+[C4(CN)6].-with respect to [MnIIITtBuPP]+[C4(CN)6].-, as evidenced by the lower θ value. The different orientations of the [C4(CN)6].- units - almost perpendicular (84.72°) for [MnIIITtBuPP]+[C4(CN)6].- and substantially tilted (32.1°) for [MnIIIOEP]+ [C4(CN)6].- may also contribute to the poorer overlap and weaker spin coupling. Hence, binding between sites with large spin densities is needed to stabilize strong ferromagnetic coupling.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/chem.19970030121
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  • 3
    Electronic Resource
    Electronic Resource
    Kinetics of the oxidation of cotton with hypochlorite in the pH range 5-10 (1962)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 58 (1962), S. 991-1008 
    Details
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The rate of consumption of oxygen by cotton and cottom cellulose from solutions of hypochlorite in the pH range 5-10 has been studied. Kinetic plots were obtained either by periodically titrating aliquots or by automatically recording the amount of alkali required to keep the pH constant. In the case of pure cotton cellulose the plots are linear, whereas in the case of cotton the plots consist of two parts, an initial, rapid oxidation of the impurities followed by a slower, linear oxidation of the cellulose. The dependence of the rate of oxidation on the pH may be expressed by: \documentclass{article}\pagestyle{empty}\begin{document}$$ {{ - dC} \mathord{\left/ {\vphantom {{ - dC} {dt}}} \right. \kern-\nulldelimiterspace} {dt}} = kC^2 _{{\rm HOCl}} C^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} _{{\rm ClO - }}$$\end{document} which also accounts for the dependence of the rate on the initial concentration of oxidant. A mechanism is suggested in terms of the free-radical OH and Cl2OOH.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1962.1205816661
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  • 4
    Electronic Resource
    Electronic Resource
    Functional groups and degradation of cotton oxidized by hypochlorite (1962)
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 58 (1962), S. 1023-1037 
    Details
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Functional groups and degradation of cotton oxidized by hypochlorite at several pH values in the range 5-10 were studied. The carboxyl group content of the oxidized cottons increases, while the aldehyde and ketone group contents decrease with increase in pH. Approximately 40% of the oxidant consumed is accounted for by the functional groups at all pH values. The ratio of carboxyl, aldehyde, and ketone groups formed per scission is 1-1.5:3:3.5 at the acidic pH range and 5:0.8:0.0 at pH 10. Oxygen consumption per scission is 26 atoms, out of which 10.4 atoms are accounted for by the functional groups. The rest of the oxygen is explained by oxidation of the soluble products of the short chain material in the fiber phase and by the functional groups of the short chains with D.P. up to 37. The degradation was found to be random at the whole pH range studied, as proved by the ratio of the number-average and weight-average molecular weights and by the linearity of the plot of log [η] vs. log (Oc + Oc0) where Oc is the oxygen consumed and Oco a constant. It is suggested that the degradation and oxidation reactions occur simultaneously and, at a given pH, with similar rates, so that all carbon atoms of an anhydroglucose unit in all chains of the amorphous phase will have a similar probability of being attacked.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1962.1205816663
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  • 5
    Electronic Resource
    Electronic Resource
    Studies on the chemical syntheses and on the characteristics of polyaniline derivatives (1995)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1227-1234 
    Details
    ISSN: 0887-624X
    Keywords: polyanilines ; derivatives ; chemical synthesis ; oxidation state ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses of parent polyaniline and methyl, methoxy, and ethoxy ortho-substituted polyanilines were performed using the conventional chemical methodology and monitored using the new open-circuit-potential (Voc) profile technique. The intermediate pernigraniline oxidation state was identified and isolated at the Voc maximum (A) during the conventional chemical synthesis of poly(o-methoxyaniline) in the emeraldine oxidation state. The introduction of the substituent on the aniline ring leads to longer polymerization times and lower Voc values. Syntheses in the presence of two different monomers in solution were also investigated and showed preferential polymerization of the monomer with the lowest Voc potential. All polymers produced were characterized by elemental analysis, gel permeation chromatography, UV-VIS spectroscopy, and cyclic voltammetry. The influence of the substituent on the Voc profile and on the polymer characteristics are rationalized in terms of steric and electronic effects. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1995.080330805
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  • 6
    Electronic Resource
    Electronic Resource
    Magnetic field induced reversed (Negative) magnetization for electrochemically deposited Tc = 260 K Oxidized Films of Chromium Cyanide MagnetsWe gratefully acknowledge support from the US National Science Foundation, Grant no. CHE-9320478, Department of Energy, Division of Materials Science, Grant no. DE-FG02-86ER45271.A000, Department of Energy, Division of Advanced Energy Projects, Grant no. DE-FG02-96ER12198, and the Office of Naval Research. (1997)
    Weinheim : Wiley-Blackwell
    Advanced Materials 9 (1997), S. 645-647 
    Details
    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
    URL: http://dx.doi.org/10.1002/adma.19970090812
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  • 7
    Electronic Resource
    Electronic Resource
    Studies of the effect of fiber surface and matrix rheological properties on nonwoven reinforced elastomer composites (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 751-765 
    Details
    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 fiber type and fiber-surface properties on matrix flow behavior was investigated using structural reaction injection-molding (SRIM). The influence of fiber type, fiber-surface properties, and matrix type on strength properties in elastomeric composites reinforced with nonwoven fibrous structures was investigated using tensile tests on elastomer composite samples from SRIM and latex coagulation (LC) fabrication methods and the microbond strength method on individual fibers. The fibers used were PET, LLDPE, and p-aramid. Fibers were treated with epoxy, styrene, and isocyanate derivatives, which make the surface chemically reactive. Treatments were also made with NaOH and a copolymer of polyester and polyol ether, causing a change in the fiber surface energy. The matrix types were polyurethane elastomer and natural rubber. The results show that the surface treatments which produced a change in the surface energy influenced the flow rate of the matrix polymer during the composite fabrication process. The treatments resulted in chemically reactive fiber surfaces which improved the fiber-matrix bond strength without affecting the Young's modulus of the composite material. Good correlation was found between bond strength and surface energy including the dispersive component of surface energy in the case of polyurethane elastomer and surface-modified PET fibers. The age of the polyurethane matrix has a marked influence on the bond strength. The fiber volume fraction in composites has a strong influence on the Young's modulus of the elastomer composite. © 1995 John Wiley & Sons, Inc.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1995.070570610
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  • 8
    Electronic Resource
    Electronic Resource
    Copolymers in dilute solution. I. Preliminary results for styrene-methyl methacrylateWork supported in part by Office of Ordnance Research. (1996)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1005-1018 
    Details
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dilute solution properties of copolymers are briefly discussed in relation to those of the parent homopolymers. It is shown that copolymer molecules are usually more expanded in solution than would be expected from the averaged behavior of the pure polymers, because of repulsive interactions between the unlike monomer units. A thermodynamic parameter χAB characterizing these interactions can be derived from measurements of the dilute solution properties of copolymers. In favorable cases this parameter can be independently evaluated from studies of ternary systems composed of the two parent homopolymers and a solvent, thus allowing prediction of the behavior of the copolymer. Light scattering and viscosity measurements on fractions of approximately equimolal copolymers of styrene and methyl methacrylate are presented and analyzed. The values of χAB deduced from the results in two solvents agree satisfactorily with each other, but are somewhat larger than those earlier obtained from measurements on ternary systems.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/polb.1996.905
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  • 9
    Electronic Resource
    Electronic Resource
    Immobilized pH gradient two-dimensional gel electrophoresis and mass spectrometric identification of cytokine-regulated proteins in ME-180 cervical carcinoma cells (1997)
    Weinheim : Wiley-Blackwell
    Electrophoresis 18 (1997), S. 409-417 
    Details
    ISSN: 0173-0835
    Keywords: Cervical carcinoma ; Two-dimensional polyacrylamide gel electrophoresis ; Mass spectrometry ; Immobilized pH gradient ; Cytokine ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Two-dimensional (2-D) polyacrylamide gel electrophoresis combined with mass spectrometry is a powerful combination of technologies that allows high resolution separation of proteins and their rapid identification. Immobilized pH gradient (IPG) first-dimensional gels have several advantages over carrier ampholyte isoelectric focusing, including a high degree of reproducibility, good protein spot resolution, and a selection of pH range. Here we demonstrate the utility and efficacy of combining IPG 2-D gel electrophoresis with mass spectrometry to identify interferon-γ- (IFN) and tumor necrosis factor (TNF)-regulated proteins in ME-180 cervical carcinoma cells. Three cytokine-regulated proteins have been identified, using imidazole-zinc-stained preparative IPG 2-D gels and in-gel tryptic digestion followed by matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry for determination of peptide masses and sequences: (1) triosephosphate isomerase, a glycolytic pathway enzyme, (2) proteasome subunit C3, which is important in protein degradation, and (3) Ran, a GTP-binding protein important in cell cycle regulation, protein import into the nucleus, and RNA export from the nucleus.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/elps.1150180315
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  • 10
    Electronic Resource
    Electronic Resource
    Identification of cytokine-regulated proteins in normal and malignant cells by the combination of two-dimensional polyacrylamide gel electrophoresis, mass spectrometry, Edman degradation and immunoblotting and approaches to the analysis of their functional roles (1996)
    Weinheim : Wiley-Blackwell
    Electrophoresis 17 (1996), S. 1655-1670 
    Details
    ISSN: 0173-0835
    Keywords: Protein identification ; Cytokine-regulated proteins ; Mass spectrometry ; Interferon -γ ; Tumor necrosis factor ; Malignancy ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/elps.1150171103
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