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  • 1
    ISSN: 1573-9171
    Keywords: catalytic systems ; cyclotrimerization ; isocyanates ; hydrogen bonds ; molecular complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The rate of cyclotrimerization of phenyl isocyanate in chlorobenzene at 120 °C in the presence of the tertiary amine-α-oxide-proton donor (PD) ternary catalytic system has been studied using a dual calorimeter and a series of phenols with various acidities as the PD. In the presence of weakly acidic phenols, complexes of quaternary ammonium type bases are formed in the ternary catalytic systems. Acidic phenols afford salt complexes with the transfer or a proton from phenol to the tertiary amine in a quantitative yield, while the α-oxide present remains unaffected. The structures of the complexes were studied by IR and by IR and1H NMR spectroscopy.
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  • 2
    ISSN: 1573-9171
    Keywords: isocyanate polycyclotrimerization catalysts ; X-ray analysis ; molecular complexes ; strong H-bonds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A 1∶1-complex of trinitrophenol with benzyldimethylamine (1) and a 1∶1∶1-complex, the product of the interaction of benzyldimethylamine, glycidyl phenyl ether, and phenol (2), have been synthesized and characterized by means of X-ray analysis. Complex1 is a precursor for the catalysts of selective isocyanate cyclotrimerization, while complex2 is one of those catalysts. In the crystal structure complex1 forms H-bonded cationic-anionic aggregates with proton transfer from phenol to the N-atom of the tertiary amine. Complex2 crystallizes as a monohydrate (2a) with a strong H-bond between the quaternary ammonium and phenolic components, and exists in crystals in the form of globular H-bonded dimeric hydrates. Possible pathways of dissociation of complex2a are discussed. The data obtained may be used as a basis for further interpretation of the regularities of cyclotrimerization of isocyanates catalyzed by complexes of this type.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 18 (1992), S. 487-490 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The surface and mechanical properties of thin Cr films play an essential role in microphotolithographic processes in which an inorganic photoresist based on vacuum-evaporated As2S3 is used as a light-sensitive system. The present paper reports some XPS data about thin chromium layers obtained by thermal evaporation, high-frequency sputtering, electron beam evaporation and de magnetron sputtering. A correlation is found between the surface elemental composition of the metal coating and the metal coating and the possibilities of obtaining good adhesion between the Cr and As2S3 used as the inorganic photoresist. It is shown that the presence of pure Cr on the surface of the samples is a defining condition for photolithography in the submicron region.
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 22 (1994), S. 202-205 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: This paper reports some XPS data on unexposed and exposed thin films of As2S3 deposited onto chromium-coated glass substrates. We show the chemical changes on the surface and interface of As2S3 and chromium layers. The chromium layers are obtained by thermal evaporation, high-frequency sputtering and electron beam evaporation. Chemical changes of the sample surface after laser irradiation are investigated. Exposure of As2S3 films results in photo-induced oxidation of arsenic on the surface and formation of As2O3. It is established that the O 1s peak area on exposed samples decreases compared to the O 1s peak area on unexposed ones. This is related to desorption of As2O3 from the surface of exposed As2S3 layers. Another proof of desorption of As2O3 is the decrease of the As 3d/S 2p normalized peak area ratio on exposed As2S3 layers. The sulphur content on the surface remains unchanged after exposure of the samples, but its chemical surroundings change. An alteration of the chemical environment of As and Cr is observed at the As2S3/Cr interface, due to diffusion of chromium atoms through the interface into the As2S3 layer. This results in formation of an AsxCrySz compound at the As2S3/Cr interface, which dissolves with a lower rate. This hinders further etching of the metal coating during the photolithographic process employing Cr plates with inorganic photoresist based on vacuum deposited As2S3.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 39 (1988), S. 555-558 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die Möglichkeiten zur Herstellung von Acryllatices durch Emulsionscopolymerisation von Ethylacrylat, Methylmethacrylat und Methacrylsäure wurden untersucht. Es wurde festgestellt, daß die Dosiergeschwindigkeit des Monomer-gemisches die Eigenschaften des Latex beeinflußt. Die optimale Dosiergeschwindigkeit, bei der die Latices und die daraus gewonnenen Filme die besten Eigenschaften aufweisen, wurde ermittelt.
    Notes: The possibility to obtain acrylic latices by emulsion copolymerization of ethyl acrylate, methyl methacrylate and methacrylic acid has been studied. It has been found that the rate of dosing of the monomer composition affects the qualities of the latex. The optimal rate of dosing at which the latices and films thereof possess the best characteristics has been determined.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 41 (1990), S. 338-341 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die rheologischen Eigenschaften von durch Emulsionspolymerisation von Ethylacrylat, Methylmethacrylat und Acrylsäure erhaltenen Acrylat-Dispersionen wurden untersucht. Diese wäßrigen Dispersionen sind Nicht-Newtonsche pseudoplastische Flüssigkeiten, deren scheinbare Viskosität bei konstanter Schergeschwindigkeit sowohl vom pH-Wert des Mediums als auch von der Emulgatormenge und von der Menge des eingesetzten carboxylierten Agens abhängt. Die Anwendbarkeit der de-Broyn-Gleichung wurde geprüft, und die Quellungskoeffizienten wurden bestimmt.
    Notes: The rheological properties of acrylic latices obtained by emulsion polymerization of ethyl acrylate, methyl methacrylate, and methacrylic acid have been studied. These water dispersions are non-Newtonian pseudoplastic liquids, whose apparent viscosity at constant shear rate depends on the pH of the medium as well as on the amounts of the emulgator and carboxylated agent used. The applicability of the de-Broyn equation has been examined and the coefficient of swelling has been determined.
    Additional Material: 7 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 53 (1994), S. 729-733 
    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: Acrylonitrile copolymer membranes were subjected to partial hydrolysis in order to improve their dialysis characteristics. The partial hydrolysis time and temperature, as well as the concentration of the hydrolyzing agent, were the variable parameters. The changes in the chemical and physical characteristics of the membrane were proved by infrared spectroscopy, elemental analysis, differential scanning calorimetry, and Mercury intrusion porometry. After each degree of modification, the permeability of the membrane with respect to a solution of vitamin B12 was determined under static conditions and at temperature of 298 K. The improvement in the permeability at a definite degree of hydrolysis is explained by the conversion of nitrile groups to amide and carboxyl groups, as well as increase of the volume of the pores with average radius. The efficiency of the modified PAN membranes for concentration of biological liquids (diluted serum) was studied. © 1994 John Wiley & Sons, Inc.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 777-784 
    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: Phosphorus-, zinc-, and chlorine-containing oligomer was used as a comonomer including ionic bonds in its molecules in the synthesis of poly(ethylene terephthalate). Phosphorus-, zinc-, and chlorine-containing poly(ethylene terephthalate) including ionic bonds in its main polymer chain was synthesized. With a content of 0.6% P and 1.25% Zn and 0.1% Cl, the resin has the following characteristics: ηrel = 1.407; COOH 39.90 mg equiv KOH/g 10-6; and mp 255.8°C. The modifier acts as a thermostabilizer. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1665-1676 
    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 possibility of reinforcing polyethylene (PE) by blending it with a liquid crystalline polymer (LCP) rests on the successful improvement of phase compatibility and interfacial adhesion of these two structurally unlike polymers. The approach that is being considered in our laboratories consists of the synthesis of PE-LCP block or graft copolymers and of their use as compatibilizing agents for PE/LCP blends. In this work, the melt polycon-densation of sebacic acid (S), 4,4′-dihydroxybiphenyl (B), and 4-hydroxybenzoic acid (H) has been carried out at temperatures up to 280°C in the presence of an oxidized low molar mass PE sample containing free carboxylic groups (PEox), with the main scope of demonstrating that a PE-g-LCP copolymer may be synthesized by this route. The polycon-densation product has been fractionated by successive extractions with boiling toluene and xylene. The soluble fractions and the residues have been characterized by IR and NMR spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TG, DTG), and scanning electron microscopy (SEM). The extractions and the analyses have been repeated on a PEox/LCP blend prepared by melt mixing PEox and preformed LCP (SBH 112, by Eniricerche). The results show that, whereas for the blend a fairly clean separation of PEox and SBH can be obtained by solvent extraction, this is not so for the polycondensation product. All analytical procedures concordantly show that a PEox-g-SBH copolymer has, in fact, been obtained. In effect, both PEox and SBH chain segments are present, with different relative ratios, in all fractions of the polycondensate. Moreover, a fairly quantitative esterification of the PEox carboxyl groups has been shown by IR analysis to take place in the adopted conditions. Preliminary morphological investigations carried out by SEM have shown that the addition of the synthesized graft copolymer into HDPE/SBH blends leads to an improvement of the interfacial adhesion. © 1996 John Wiley & Sons, Inc.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1613-1625 
    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: Reactive blends (50/50 w/w)of a low molar mass polyethylene containing free carboxylic groups (PEox) and a semiflexible liquid crystalline polyester (SBH 1:1:2, by Eniricerche) have been prepared at 240°C in a Brabender mixer, in the presence of Ti(OBu)4 catalyst, for different mixing times (15,60, and 120 min). In order to prove the formation of a PE-g-SBH copolymer, the blends have been fractionated by successive extractions with boiling toluene and xylene. The soluble fractions and the residues have been analyzed by Fourier transform infrared (FTIR) spectroscopy, thermogravimetry (TG and DTG), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). All analytical procedures concordantly show that PE-g-SBH copolymers with different compositions, arising from differences of either the number of PEox carboxylic groups entering the transesterification or the length of grafted SBH branches, are formed as a result of blending. Depending on the relative content of PE and SBH segments, the copolymers dissolve in the solvents, together with any unrreacted PEox, or remain in the residues, together with neat SBH. Qualitative IR analyses and quantitative TG measurements have shown that the amount of copolymers increases strongly with the mixing time. Preliminary SEM observations indicate that the unfractionated products of the reactive blending carried out with long (120 min) mixing times lead to improved interfacial adhesion and phase dispersion when added to PE/SBH blends. © 1996 John Wiley & Sons, Inc.
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