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  • Articles: DFG German National Licenses  (10)
  • Chemistry  (10)
  • 1
    Electronic Resource
    Electronic Resource
    Mechanism of sulphur transport through preformed oxide scales (1980)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 31 (1980), S. 682-688 
    Details
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Mechanismus des Transports von Schwefel durch vorher entstandene OxidzunderschichtenDie Möglichkeiten für den Transport von Schwefel durch vorher entstandene Oxidzunderschichten werden thermodynamisch untersucht, wobei die Grenzbedingungen ermittelt werden, unter denen die verschiedenen Mechanismen - Auflösung und Diffusion, Moleküldiffusion und Gasdiffusion - auftreten können. Die Ergebnisse werden für Nickel und Kobalt überprüft; daraus ergibt sich der Schluß, daß zwar grundsätzlich beide Mechanismen parallel vorliegen können, daß jedoch die Permeation von Gasmolekülen gefährlicher ist, da sie in einem breiteren Bereich von Gaszusammensetzungen wirksam werden kann. Außerdem wird deutlich gezeigt, daß durch die auf Kobalt aufwachsenden Oxidzunderschichten Schwefeldioxidmoleküle diffundieren können.
    Notes: The possibilities for transport of sulfur through preformed oxide scales by both solution-diffusion and molecular gas (24) permeation mechanisms are examined thermodynamically to establish the limiting conditions under which each is viable.The results are tested, using nickel and cobalt specimens, and it is concluded that, although both mechanisms may operate in parallel, the permeation of gas molecules is the more dangerous since it can operate over wider ranges of gas atmosphere composition. The permeation of SO2 molecules throu through oxide scales growing on cobalt is clearly demonstrated.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19800310903
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  • 2
    Electronic Resource
    Electronic Resource
    Studies on thermal stability of modified polycarboxylate cements (1995)
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 224 (1995), S. 109-114 
    Details
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Poly(acrylsäre-co-acrylamid) wurde mit Zinkoxid und Kryolith (Na3AlF6) in unterschiedlichen Verhältnissen gemischt und bei Raumtemperatur zu Zahnzementen ausgehärtet. IPDT, Temperaturen bei maximaler Abbaugeschwindigkeit, Aktivierungsenergien und Frequenzfaktoren des thermischen Abbaus der Proben wurden aus thermogravimetrischen Messungen ermittelt. Die Probe mit 20 Gew.-% Kryolith in der Füllstoffmischung ist thermisch sehr stabil.
    Notes: Dental cement compositions made by mixing poly(acrylic acid-co-acrylamide) and mixtures of zinc oxide and cryolite (Na3AIF6) in various proportions of 10-50 wt.-% (w/w) were cured at room temperature. From thermogravimetric analyses of the samples, the integral procedural decomposition temperatures (IPDT), maximum decomposition temperatures, activation energies and frequency factors were evaluated. The cured cement sample containing 20 wt.-% cryolite in the filler mixture is thermally very stable.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/apmc.1995.052240111
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  • 3
    Electronic Resource
    Electronic Resource
    The effect of processing variables on microstructure of injection molded short fiber reinforced polypropylene composites (1989)
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 10 (1989), S. 344-351 
    Details
    ISSN: 0272-8397
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Injection molded composites of polypropylene reinforced with short glass fibers were obtained under a variety of injection molding conditions. The microstructure of the moldings was determined using a variety of experimental techniques, including optical and scanning electron microscopy, differential scanning calorimetry, Fourier transform infra-red spectroscopy, and thermogravimetry. Thus, it was possible to obtain a detailed characterization of the crystallinity, morphology, and orientation distribution in the matrix, in addition to the distribution of fibers and their orientation of the fibers in the composite. The influence of molding conditions on the above microstructural characteristics is summarized in an effort to explain the experimental observations.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pc.750100511
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  • 4
    Electronic Resource
    Electronic Resource
    Microstructure and mechanical behavior of reinforced reaction injection molded (RRIM) polyurethane (1987)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 1258-1264 
    Details
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: A study was carried out to characterize the microstructure and distribution of some mechanical properties in reinforced reaction injection molding panels (RRIM). The panels were prepared under a variety of processing conditions. Scanning electron microscopy, differential scanning calorimetry, and Fourier transform infrared analysis were employed for microstructure characterization. The following mechanical tests were carried out: dynamic mechanical, tensile, and impact. The results indicate significant relationships between processing conditions, microstructure, and mechanical properties. In particular, the skin/core structure of the panels and the size distribution of bubbles in the matrix have an important effect on the impact properties. Furthermore, the balance between the distributions of cure and crystallinity, which is difficult to define clearly, plays an important role in determining panel behavior.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760271609
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  • 5
    Electronic Resource
    Electronic Resource
    Structural Studies on Indium and Tin Thiobenzoates (1996)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1093-1098 
    Details
    ISSN: 0009-2940
    Keywords: Indium tris(thiobenzoate) ; Triethylammonium tetrakis(thiobenzoato)indate ; Tin, butyl-, tris(thiobenzoate) ; Tin, dichloro-, bis(thiobenzoate) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indium(III) and tin(IV) thiocarboxylates were prepared and characterized on the basis of their IR, 13C- and 19Sn-NMR data. Indium tris(thiobenzoate) (1) decomposes into a sulfido complex In (S)[S(O)CPh] (2a). The corresponding tris(thioacetate) In[S(O)CMe]3 is thermally too unstable to be isolated. The anionic tetrakis complex [Et3NH]{In[S(O)CPh]4} (3) was characterized by X-ray crystallography which revealed a distorted tetrahedral coordination at the In atom. X-ray diffraction analysis of the complexes BuSn[S(O)CPh]3 (4) and Cl2Sn[S(O)CPh]2 (7) showed distorted tetrahedral and cis-octahedral structures, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19961290918
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  • 6
    Electronic Resource
    Electronic Resource
    Molecular addition compounds of tin(iv) chloride. I. Preparation and infrared spectra of the complexes of stannic chloride with certain amides (1964)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 332 (1964), S. 103-112 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Darstellung und Eigenschaften von Additionsverbindungen des SnCl4 mit N, N-Dimethylformamid, Acetamid, Acetanilid und Benzamid werden mitgeteilt. Neben der Analyse zeigen auch Donator-Acceptor-Titrationen in Dichloräthan die allgemeine Formel SnCl4 · 2 Amid. Leitfähigkeitsmessungen in Nitromethan und Molekulargewichtsbestimmungen lassen auf das Vorliegen von monomeren Additionsverbindungen schließen. Aus den IR-Spektren geht an Hand einer Erniedrigung der (C—O)- und einer Erhöhung der (C—N)-Valenzschwingung eine Bindung der organischen Liganden an das Zinn über Sauerstoff hervor. Die relativen Basenstärken nehmen in der Reihe Dimethylformamid, Benzamid, Acetanilid, Acetamid ab.
    Notes: The molecular addition compounds of tin (iv) chloride with N, N-dimethyl formamide, acetamide, acetanilide, and benzamide have been prepared. They are of the type SnCl4 · 2 amide. This composition type has been confirmed by indicator titrations of stannic chloride against amides in dichloroethane. Conductivity measurements in nitromethane and molecular weight determinations show that they are true molecular addition compounds being monomeric.The infrared spectra of the adducts show that there are metal-to-oxygen bonds in all these compounds as is evidenced by a negative shift of the carbonyl stretching frequency and a positive shift of the C—N stretching frequency. The relative donor ability of the amides towards stannic chloride has been found to be: dimethyl formamide 〉 benzamide 〉 acetanilide 〉 acetamide.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19643320112
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  • 7
    Electronic Resource
    Electronic Resource
    Studies on MM″(NCS)4 [M=Ni(II), Fe(II), Zn(II), and M″=Hg(II) Zn(II)] complexes (1976)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 423 (1976), S. 173-179 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Untersuchungen an MM″ (NCS)4-Komplexen (M = NiII, FeII, ZnII; M″ = HgII, ZnII)Komplexe des Typs MM′(NCS)4 · xL M = NiII, FeII, ZnII; M″ = HgII, ZnII; x = 2, 4, 6; L = Nicotinamid (nia), Isonicotinsaiurehydroxid (inh) 2-Aminopyrimidin (2apm)] wurden dargestellt und charakterisiert durch Elementaranalyse, molare Leitfähigkeit, magnetisches Moment, IR- und Elektronenspektren.
    Notes: Coordination complexes of the type MM″(NCS)4 · xL M = Ni(II), Fe(II), Zn(II), M″ = Hg(II), Zn(II), x = 2, 4, 6 and L = nicotinamide (nia), 3-cyanopyridine (3-cpy), 4-cyanopyridine (4cpy), 4-aminopyridine (4apy), isonicotinic acid hydrazide (inh), 2-aminopyrimidine (2apm)l have been prepared and characterized by elemental analysis, molar conductance, magnetic moment, infrared and electronic spectral studies. Molar conductance data of NiZn(NCS), complexes are equivalent to 1:1 electrolyte. The infrared spectral studies indicate that only bridged thiocyanate groups are present in the complexes of the type NiHg(SCN)4 · 4L [L=3 and 4cpy, inh] and FeHg(SCN)4 · 2L [L = nia, 2apm], whereas both bridged and terminal thiocyanates are present in the complexes of the type NiHg(SCN)4 · 4L [L = nia, 3apy and ZnHg(SCN)4 · 2(inh). BOHR magneton values and electronic spectral data indicate an octahedral environment around nickel and iron in their complexes. Symmetry and group theory have also been used to establish the structure of the complexes.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19764230211
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  • 8
    Electronic Resource
    Electronic Resource
    Studies on the Hydrazine Complexes of Some Bivalent Metal Ions in aqueous solution (1967)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 349 (1967), S. 213-219 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Für die Hydrazin-Komplexe von Mn(II), Co(II), Ni(II), Cu(II) und Zn(II) werden Zusammensetzung und Bildungskonstanten nach der Methode von Rossotti und Rossotti ermittelt, wobei experimentell pH-Titrationen in Lösungen durchgeführt wurden, die Metall-perchlorat, Hydrazin-diperchlorat und Natriumperchlorat (Ionenstärke μ = 1, t = 30°C) enthalten. In entsprechender Weise wurden die Bildungskonstanten für die Protonisierung von Hydrazin bestimmt. Selbst bei den höchsten Verhältnissen: Gesamt-Hydrazin/Gesamt-Metall (etwa 60) haben die höchsten Komplexe nur bei Co(II) und Zn(II) das Verhältnis:Metall/Hydrazin = 1 : 2, während in allen anderen Fällen in Lösung nur 1 : 1-Komplexe zu existieren scheinen.Die Werte der Bildungskonstanten (30°C, μ = 1) siehe „Summary“.Die nach Bjerrum berechneten β1-Werte sind mit den gefundenen in recht guter Übereinstimmung mit Ausnahme für Co(II). Die Grenzen für die Bjerrum-Methode werden diskutiert.
    Notes: The compositions and formation-constants of the complexes formed by Mn(II), Co(II), Ni(II), Cu(II) and Zn(II) with hydrazine have been evaluated graphically following the method of Rossotti and Rossotti using the necessary data from the results of pH titration of solutions containing the metal perchlorate, hydrazinium diperchlorate and sodium perchlorate at an ionic strength of unity at 30°C. The values of the successive equilibrium constants for the protonation of hydrazine, which were also needed, have been evaluated separately by similar procedure. Even at the rather high ratio of ca. 60 of (total hydrazine)/(total metal) the highest complexes which appear to be formed in the systems investigated have the ratio of metal:hydrazine of 1:2 for Co(II) and Zn(II), while in all the other cases only 1: 1 complexes appear to exist in solution.The values of the formation-constants (at 30°C; μ = 1) obtained are: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \log \beta _1 :{\rm Mn(II), 4}{\rm .76; Co(II), 1}{\rm .78; Ni(II),3}{\rm .18; Cu(II),6}{\rm .67;Zn(II), 3,69}{\rm.} \\ \log \beta _2 :{\rm Co(II), 3}{\rm .34; Zn(II), 6}{\rm .69}. \\ \end{array} $$\end{document}β1 values obtained from the Bjerrum relation are in fairly good agreement with those given above except for Co(II). The limitations of Bjerrum's method are discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19673490314
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  • 9
    Electronic Resource
    Electronic Resource
    Quantitative softness parameters and their application in elucidation of Structure of Bimetallic Tetrathiocyanate Complexes (1980)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 461 (1980), S. 222-230 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Quantitative „Softness“ Parameter und ihre Anwendung in der Strukturaufklärung von Bimetalltetracyanat-Komplexen〉2M(NCS)2M′(SCN)2〈 und [Ml6][M′(SCN)4], (M = COII und NiII; M′ = ZnII, CdII und HgII, L = Anilin, p-Toluidin, Pyridin, Nicotinamid, 2,2′-Bipyridin und 4-Aminopyridin) wurden dargestellt und charackterisiert. Die Strukturen werden auf Grund von Leitfähigkeits-, magnetischen und spektroskopischen (IR und VIS) Messungen, sowie durch gruppentheoretische Berechnungen und Ligandenfeldparametern vorgeschlagen. Diese Strukturvorschläge werden gestützt durch quantitative „Softness“ - Werte „\documentclass{article}\pagestyle{empty}\begin{document}$ {\rm E}_{\rm n}^{_ + ^ +},{\rm E}_{\rm m}^{_{\rm +}^{\rm +}} $\end{document}“. Die totale „Softness“ von M und M′ und ihre Differenz \documentclass{article}\pagestyle{empty}\begin{document}$ \Delta {\rm TE}_{\rm n}^{_ + ^ +} \left({{\rm M} - {\rm M}'} \right) $\end{document} wurden abgeleitet (Gleichungen siehe Abstract) und mit der Struktur der Komplexe in Verbindung gebracht.
    Notes: 〉2M(NCS)2M′(SCN)2〈 and [ML6][M′(SCN)4], (M = Co(II) and Ni(II), M′ = Zn(II), Cd(II) and Hg(II) and L = aniline(ani), p-toluidine(tol), pyridine(py), nicotinamide(nia), 2,2′-bipyridine(bipy) and 4-aminopyridine (apy)) have been prepared and characterized. Their structure have been proposed on the basis of molar conductance, magnetic moment, group theoretical calculations, ligand field parameters, infrared and electronic spectral studies. The proposed structures have also been supported by quantitative values of softness „\documentclass{article}\pagestyle{empty}\begin{document}$ {\rm E}_{\rm n}^{_ + ^ +},{\rm E}_{\rm m}^{_{\rm +}^{\rm +}} $\end{document}“,. Total softness of M and M′ and their difference \documentclass{article}\pagestyle{empty}\begin{document}$ \Delta {\rm TE}_{\rm n}^{_ + ^ +} \left({{\rm M} - {\rm M}'} \right) $\end{document} have also been derived by the following equations and related to the structure of the complexes. \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm TE}_{\rm n}^{_ + ^ +} \left({\rm M} \right) = {\rm E}_{\rm n}^{_ + ^ +} \left({\rm M} \right) + \sum {\rm E}_{\rm m}^{_ + ^ +} \left({\rm L} \right) + \sum {\rm E}_{\rm m}^{_ + ^ +} \left({{\rm NCS}} \right) $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm TE}_{\rm n}^{_ + ^ +} \left({{\rm M}}^\prime \right) = {\rm E}_{\rm n}^{_ + ^ +} \left({{\rm M}}^\prime \right) + \sum {\rm E}_{\rm m}^{_ + ^ +} \left({\rm L} \right) + \sum {\rm E}_{\rm m}^{_ + ^ +} \left({{\rm SCN}} \right) $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta {\rm TE}_{\rm n}^{_ + ^ +} \left({{\rm M} - {\rm M}^\prime} \right) = \,|\,{\rm TE}_{\rm n}^{_ + ^ +} \left({\rm M} \right) - {\rm TE}_{\rm n}^{_ + ^ +} \left({{\rm M}}^\prime \right)$$\end{document}.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19804610134
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  • 10
    Electronic Resource
    Electronic Resource
    TSDC studies on thermoelectrets of CR-39(DOP) (1990)
    Weinheim : Wiley-Blackwell
    Acta Polymerica 41 (1990), S. 48-51 
    Details
    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: Aus dem Polymer CR-39(DOP) wurden Thermoelektrete formiert, und die thermisch stimulierten Entladungsströme wurden gemessen. Die Einflüsse unterschiedlicher Formierungstemperaturen, unterschiedlicher Feldstärken und der Lagerzeit wurden untersucht, um das Elektretverhalten dieses Materials zu beschreiben. Die Polarisation ist dipolaren Ursprungs. Die Aktivierungsenergic und die Relaxationszeit wurden berechnet.
    Notes: Thermoelectrets of CR-39(DOP) were formed and their thermally stimulated discharge current studied. In the present work, effects of different forming temperatures, polarizing fields and storage times have been studies with a view to understand the electret behaviour of this material. The polarization seems to have a dipolar origin. The activation energy and relaxation times have also been calculated.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/actp.1990.010410112
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