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  • Chemical Engineering  (77)
  • Aerodynamics
  • Fluid Mechanics and Thermodynamics
  • GENERAL
  • Inorganic Chemistry
  • 1990-1994  (112)
  • 1955-1959
  • 1991  (112)
Collection
Publisher
Years
  • 1990-1994  (112)
  • 1955-1959
Year
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 1895-1899 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 37 (1991), S. 1900-1903 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 592-595 
    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: Reinforced plastics based on poly(cyclohexanedimethylene terephthalate) (PCT) are excellent for electrical and electronic applications, particularly in the manufacture of electrical connectors. PCT offers a high heat deflection temperature, low cost, and relative ease of processing. For the injection molding process, stability of the melt is an important consideration, especially for materials with high melting points such as PCT. The combination of the polyester resin with flame retardant additives, processing aids, and thermal stabilizers results in a number of competing reactions which can change the molecular weight and molecular-weight distribution (MWD) of the base polymer in the composite. Typical analytical techniques such as melt or dilute solution viscosity do not give adequate means of monitoring these changes so as to allow the polymer chemist to determine the effects of various additives on MWD. Size-exclusion chromatography (SEC), by virtue of providing information on the entire MWD, was found suitable to study molecular-weight changes in the melt due to both branching and chain cleavage, even when both phenomena occur simultaneously. Changes in the MWD over time at processing temperatures can be used to determine kinetic parameters and have been used to optimize PCT additive formulations for best processability and mechanical property retention.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 1665-1669 
    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: The Differential Scanning Calorimetry (DSC) trace for a commercial phenolic resole resin shows two distinct peaks. Assuming that these represent two independent cure reactions results in a kinetic model of the form: \documentclass{article}\pagestyle{empty}\begin{document}$$ \frac{{dx}}{{dt}} = p\kappa _1 \left({1 - x_1} \right)^{n_1} + \left({1 - p} \right)\kappa _2 \left({1 - x_2} \right)^{n_2} $$\end{document} with κi = κio exp(-Bi/T).The Arrhenius parameters were estimated from a plot of ln(β/Tp2) versus 1/Tp. The parameters, p, n1, and n2 were obtained by writing the DSC response predicted by the equation above in terms of a function which contains temperature as the only variable. \documentclass{article}\pagestyle{empty}\begin{document}$$ \dot q = q_{tot} \left[{p\kappa _1 \left({1 - \theta _1 /r_1} \right)^{r_1 - 1} + \left({1 - p} \right)\kappa _2 \left({1 - \theta _2 /2} \right)^{r_2 - 1}} \right] $$\end{document} with \documentclass{article}\pagestyle{empty}\begin{document}$ \theta _i = \left({1/\beta} \right)\int_{T_0}^T {\kappa _i dT \le r_i} $\end{document} dT ≤ ri and ri = 1/(1-ni).Fitting this equation to the DSC response measured at a scan rate of 4°C/min obtains p ≈ 0.66; n1 ≈ 0.55; n2 ≈ 2.2; B1 ≈ 8285; B2 ≈ 7480; κ1 ≈ 1. 12 × 108 s-1; κ2 ≈ 0.99 × 106 S-1.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 12 (1991), S. 333-337 
    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: The effect of water absorption on the stress transferability across E-glass fiber/nylon 6 interface has been studied using the embedded single fiber composite technique. The behavior of silane coated fiber and untreated fiber composites after periods of water immersion were compared. The silane coating provided both higher interfacial shear stress transferability and protection from permanent water damage in the interphase region. It was found that water absorption in the nylon matrix reduced the shear stress transferability through plasticization of the matrix, weakening of the interface, and the development of tensile swelling stresses at the phase boundaries. In untreated materials the shear stress transferability was limited by decoupling of the matrix from the broken fiber ends by either interface slippage or local plane strain fracture in the interphase region near the fiber end. In the silane treated materials the shear stress transferability was limited by constrained yielding of the polysiloxane/nylon interphase at the fiber end, thus indicating plasticization of the matrix was the primary factor. After 20 days of water immersion, there was permanent deterioration of stress transferability in the untreated samples, but very little permanent damage in the treated samples.
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Brookfield, Conn. : Wiley-Blackwell
    Polymer Composites 12 (1991), S. 391-403 
    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: The primary goal of this study was to develop 2-D and 3-D computer simulation schemes for the mold filling processes of structural reaction injection molding (SRIM) and resin transfer molding (RTM) under isothermal conditions. The developed computer code was able to simulate the mold filling in molds with complicated geometry, Experiments were also carried out based on flow vitalizations. Experimental results were compared with the numerical simulations.
    Additional Material: 11 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 603 (1991), S. 69-76 
    ISSN: 0044-2313
    Keywords: Dicesium mercury(II) palladium(II) hexachloride ; preparation ; crystal structure ; group-subgroup relation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Crystal Structure of Cs2HgPdCl6, a Distorted Variant of ChloroperovskitsCs2HgPdCl6 single crystals show tetragonal symmetry with the space group I 4/m m m (No. 139) with 2 formular units per unit cell. The lattice parameters are a = 7.432(4) Å, c = 10.874(7) Å. The atomic arrangement of Cs2HgPdCl6 is explored by X-ray crystal structure analysis. The important polyhedrons are square-planar PdCl4 groups and HgCl2 dumbbells. The PdCl4 group is completed by two further chlorine atoms to a elongated octahedron and four further chlorine atoms form with the HgCl2 dumbbell a compressed octahedron. The crystal structure of Cs2HgPdCl6 is compared with the arrangement in halogenoperovskits and in Rb2PdCl4 [3].
    Notes: Die Verbindung Cs2HgIIPdIICl6 läßt sich durch Festkörperreaktion phasenrein darstellen. Sie kristallisiert in der Raumgruppe I 4/m m m (No. 139) mit a = 7,432(4) Å, c = 10,874(7) Å, Z = 2. Die Kristallstruktur wurde mit röntgenographischen Methoden an Einkristallen ermittelt. Pd2+ ist quadratisch-planar und Hg2+ hantelförmig von Cl-umgeben. In zweiter Nachbarschaft ergänzen weitere Cl- zu gestreckten bzw. gestauchten Oktaedern. Dieses Bauprinzip entspricht dem Aufbau von Cs2AuIAuIIICl6 [1, 2]. Es besteht direkte kristallchemische Beziehung zur Kristallstruktur der Halogenoperowskite bzw. des K2PdCl4-Typs.
    Additional Material: 4 Ill.
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  • 8
    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: This work presents the characterization of fibrous reinforcement mats in resin injection molding. The fiber mat characterization involved determining the mat permeability and compressibility. Mold filling experiments were conducted using two or more different fiber types in the mat stack, which created transverse porosity, permeability, and compressibility variations. The effect of these variations was studied by taking flow pressure measurements and observing the progress of the flow front of a non-reactive fluid filling a clear acrylic mold that contained the reinforcement mat stack.
    Additional Material: 12 Ill.
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  • 9
    Publication Date: 2018-06-05
    Description: A study of instabilities in incompressible boundary-layer flow on a flat plate is conducted by spatial direct numerical simulation (DNS) of the Navier-Stokes equations. Here, the DNS results are used to critically evaluate the results obtained using parabolized stability equations (PSE) theory and to study mechanisms associated with breakdown from laminar to turbulent flow. Three test cases are considered: two-dimensional Tollmien-Schlichting wave propagation, subharmonic instability breakdown, and oblique-wave break-down. The instability modes predicted by PSE theory are in good quantitative agreement with the DNS results, except a small discrepancy is evident in the mean-flow distortion component of the 2-D test problem. This discrepancy is attributed to far-field boundary- condition differences. Both DNS and PSE theory results show several modal discrepancies when compared with the experiments of subharmonic breakdown. Computations that allow for a small adverse pressure gradient in the basic flow and a variation of the disturbance frequency result in better agreement with the experiments.
    Keywords: Fluid Mechanics and Thermodynamics
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  • 10
    ISSN: 0009-2940
    Keywords: Manganates, carbonyl, trinuclear ; Indium-manganese clusters ; Spiro cluster ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Trinuclear Carbonylmanganates and Their Reaction Products with InCl3; X-ray Structure Determinations of K3[Mn3(μ-CO)2(CO)10], [(C6H5)4As]2[(μ-H)Mn3(μ-CO)10], [{(C6H5)3P}2N]2[μ-H)Mn3(CO)12], [(C6H5)4As]2[{μ-H)Mn3(CO)12}2(μ4-In)] und [(C6H5)4As]2[{(μ-H)Mn3(CO)12}(μ3-In){Mn(CO)5}Cl]Mn2(CO)10 reacts with KOH in aqueous solution to give the potassium carbonylmanganate K3[Mn3(μ-CO)2(CO)10] (1). The trianion 1 is isoelectronic with Fe3(CO)12 and is protonated with methanol to form the μ-hydrido cluster [(μ-H)Mn3;-(CO)12]3⊖, which is precipitated with [{(C6H5)3P}2N]Cl as [{(C6H5)3P}2N]2[(μ-H)Mn3(CO)12] (2), whereas the carbonyl-bridged μ-hydrido species [(μ-H)Mn3(μ-CO)2(CO)10]2⊖ seems to be trapped as the [(C6H5)4As]⊕ salt 3. The reaction of 3 with InCl3 yields the Mn-In clusters [(C6H5)4As]2[{(μ-H)Mn3(CO)12}2;-(μ4-In) (4) and [(C6H5)4As]2[{(μ-H)Mn3(CO)12}(μ3-In){Mn(CO)5}Cl] (5). X-ray structure analyses have been carried out for the compounds 1 - 5.
    Additional Material: 7 Ill.
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