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  • Articles  (36)
  • Chemistry  (36)
  • 2015-2019  (1)
  • 1985-1989  (25)
  • 1970-1974  (7)
  • 1945-1949  (3)
  • Physics  (36)
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  • Articles  (36)
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  • 1
    Electronic Resource
    Electronic Resource
    A semi-empirical algorithm for flow balancing in multi-cavity transfer molding (1989)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 749-761 
    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: Multi-cavity transfer molding is an important process step in several electronic and photonic technologies. In some applications, uniform filling of the cavities of the mold, or mold balancing, is required. A semi-empirical flow model to predict mold filling patterns was developed. The algorithm is a one-dimensional network flow simulation that uses experimental pressure drop data to determine the volumetric flow rate through the gates and runners. A comprehensive experimental program was undertaken to determine these hydraulic resistances for different flow rates and mold geometries. A theoretical treatment is also described to compute hydraulic resistance from gate geometry. Uniform gate resistances provide unbalanced filling and higher velocities in the cavities. Balanced filling can significantly reduce the molding compound velocity and the flow induced stresses, but imperfect balancing compromises the benefits. Experimental filling patterns were obtained for two sets of gates. The agreement between the model and the experiments was satisfactory, and the discrepancies were attributed to correctable phenomena.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760291108
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  • 2
    Electronic Resource
    Electronic Resource
    “A semi-empirical algorithm for flow balancing in multi-cavity transfer molding” (1989)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 29 (1989), S. 1796-1796 
    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
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760292409
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  • 3
    Electronic Resource
    Electronic Resource
    A new approach to capillary viscometry of thermoset transfer molding compounds (1986)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 26 (1986), S. 1399-1404 
    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 new capillary rheometer incorporated in an instrumented transfer molding press has been developed. This rheometer is effective for determining the viscosity characteristics of thermoset molding compounds under both isothermal and typical molding conditions. In examples of the rheometer's utility, the power law indices of two commercial epoxy molding compounds have been determined to be approximately 0.7. Additionally it has been shown that preconditioning typical epoxy compounds at 47 percent relative humidity causes a viscosity decrease of about 40 percent owing to plasticization of the epoxy resin.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760262008
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  • 4
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    Dissociation of antitumor potency from anthracycline cardiotoxicity in a doxorubicin analog (1985)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1985-06-28
    Description: The search for new congeners of the leading anticancer drug doxorubicin has led to an analog that is approximately 1000 times more potent, noncardiotoxic at therapeutic dose levels, and non-cross-resistant with doxorubicin. The new anthracycline, 3'-deamino-3'-(3-cyano-4-morpholinyl)doxorubicin (MRA-CN), is produced by incorporation of the 3' amino group of doxorubicin in a new cyanomorpholinyl ring. The marked increase in potency was observed against human ovarian and breast carcinomas in vitro; it was not accompanied by an increase in cardiotoxicity in fetal mouse heart cultures. Doxorubicin and MRA-CN both produced typical cardiac ultrastructural and biochemical changes, but at equimolar concentrations. In addition, MRA-CN was not cross-resistant with doxorubicin in a variant of the human sarcoma cell line MES-SA selected for resistance to doxorubicin. Thus antitumor efficacy was dissociated from both cardiotoxicity and cross-resistance by this modification of anthracycline structure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sikic, B I -- Ehsan, M N -- Harker, W G -- Friend, N F -- Brown, B W -- Newman, R A -- Hacker, M P -- Acton, E M -- CA 24543/CA/NCI NIH HHS/ -- CA 32250/CA/NCI NIH HHS/ -- CA 33303/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1985 Jun 28;228(4707):1544-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/4012308" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Antineoplastic Agents ; Breast Neoplasms/drug therapy ; Cell Line ; Chemical Phenomena ; Chemistry ; Dose-Response Relationship, Drug ; Doxorubicin/adverse effects/*analogs & derivatives/therapeutic use ; Female ; Heart/drug effects ; Humans ; Isoenzymes ; L-Lactate Dehydrogenase/analysis ; Mice ; Myocardium/enzymology ; Ovarian Neoplasms/drug therapy ; Pregnancy
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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    PAPER CURRENT
  • 5
    Electronic Resource
    Electronic Resource
    Isolation and properties of fluorescent components associated with calcified tissue collagen (1971)
    Springer
    Calcified tissue international 8 (1971), S. 197-210 
    Details
    ISSN: 1432-0827
    Keywords: Fluorescence ; Calcium ; Collagen ; Chemistry ; Bone ; Dentine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé Des composants fluorescents de l'os et la dentine sont séparés des hydrolysats alcalins de leur marice sur des colonnes Sephadex C25 CM d'échange cationique. Les concentrations en fluorescence et le spectre d'excitation (λ max 330 nm) et d'émission (λ max 395 nm) sont les mêmes que ceux observés au niveau des matrices intactes et gélatinisées. Les paramètres de fluorescence ne sont pas altérés par hydrolyse. La filtration sur gel à l'aide de colonnes Sephadex G 10 perment de différencier le matériel isolé en deux composants, ayant la même fluorescence et la même absorption UV. La fluorescence est indépendante de pH de 3.5–9.5. Des études de dialyse et de filtration sur gel de matrices gélatinisées indiquent une association étroite du matériel fluorescent avec les chaines polypeptidiques de collagène.
    Abstract: Zusammenfassung Fluorescierende Bestandteile aus Knochen und Dentin wurden in Sephadex C25 CM Kationen-Austauschersäulen von alkalischen Hydrolysaten ihrer Matrices getrennt. Die Fluorescenzintensitäten sowie die Erregungs- (λ max 330 nm) und Emissions- (λ max 395 nm) Spektren waren dieselben wie bei intakten und gelatinisierten Matrices. Die Fluorescenzparameter wurden durch die Hydrolyse nicht verändert. Eine Gelfiltration über Sephadex-G10-Säulen trennte das isolierte Material in 2 Komponenten auf, welche gleiche Fluorescenz- und UV-Absorptionseigenschaften zeigten. Im pH-Bereich zwischen 3,5 und 9,5 war die Fluorescenz unabhängig vom pH. Dialysierversuche sowie Gelfiltrationsexperimente mitden gelatinisierten Matrices zeigten eine starkgefügte Bindung des fluorescierenden Materials mit den Polypeptidketten des Kollagens.
    Notes: Abstract Fluorescent components in bone and dentine were separated from alkaline hydrolysates of their matrices on Sephadex C25 CM cationic exchange columns. The fluorescence levels, and the excitation (λ max 330 nm) and emission (λ max 395 nm) spectra, were the same as those observed in the intact and gelatinised matrices. The fluorescence parameters were unaltered by the hydrolysis procedure. Gel filtration on Sephadex G. 10 columns further resolved the isolated material into two components with the same fluorescence and UV absorption properties. The fluorescence was independent of pH over the range 3.5–9.5. Dialysis and gel filtration studies on the gelatinised matrices indicated a firmly-bonded association of the fluorescent material with the collagen polypeptide chains.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02010138
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  • 6
    Electronic Resource
    Electronic Resource
    Studies in the properties of nylon 6-glass fiber composites (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 165-175 
    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: Caprolactam has been anionically polymerized within the planar-random continuous glass mat reinforcement using a technique similar to reaction injection molding and up to 55% (w/w) [i.e., 33% (v/v)] glass fiber loading was achieved. The fiber volume fraction distribution across the diameter of the composite was observed to be reasonably uniform. The tensile stress-strain properties were determined. Composite modulus and strength appeared to be linearly dependent on the fiber volume fraction and increase with fiber volume content. The type of composite material studied has been used for compression molding of articles. Therefore, some tensile data were redetermined after compression molding and possible changes in degree of crystallinity resulting from the change in the thermal history monitored by differential scanning calorimetry. A 50% drop in the percent degree of crystallinity (monoclinic modification) of the as-polymerized composite and a deterioration in the tensile properties of the composite were observed after compression molding. On compression molding the mold surface needs to be completely covered with the composite sheet material; otherwise, matrix polymer flows out of the composite, and areas deficient in reinforcement result.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070360113
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  • 7
    Electronic Resource
    Electronic Resource
    Impact fracture behavior of continuous glass fiber-reinforced nylon 6 (1989)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 37 (1989), S. 77-89 
    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 impact fracture toughness of nylon 6/continuous glass fiber composites at four levels of fiber content has been studied. The composites were produced by anionically polymerizing caprolactam within a glass mat using a vacuum injection technique. Application of linear elastic fracture mechanics to characterize the impact fracture toughness of the composites, using an energy approach (GIC), has been found to be applicable provided that a correction is made for the size of the damage zone. The concept of Jc, fracture energy per unit ligament area, has also been applied to the composites and agreement between GIC and Jc has been found to be reasonably satisfactory. The ratio of crack propagation energy to the total energy absorbed (ductility index) has also been calculated. The ductility index was found to be close to one for the composites, indicating that additional energy is involved in propagating the fracturing cracks probably due to fiber debonding and/or crack blunting and fiber pullout. Fractographic examination of the impact fracture surface confirmed the presence of these features.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1989.070370107
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  • 8
    Electronic Resource
    Electronic Resource
    Volume change and the nonlinearly thermo-viscoelastic constitution of polymers (1987)
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 27 (1987), S. 86-100 
    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: The time-dependent behavior of linearly viscoelastic materials is known to be very sensitive to changes in temperature and in solvent (water) concentration. Following an investigation by the authors of this sensitivity in terms of the associated small volume changes, a nonlinearly viscoelastic model of constitutive behavior was formulated earlier in terms of the free volume concept and evaluated in terms of experiments on poly(vinyl acetate). Following a brief presentation of the earlier results these concepts are expanded and refined in the present paper to deal with transient deformation histories under pressure. In this connection, model computations explore the effect of simultaneous pressurization and straining. In addition the effect of “ageing” the polymer under pressures of various magnitudes and for different lengths of time are investigated. It becomes clear that the yield phenomenon depends sensitively on pressure and on the ageing time. In addition, the volume change under transient thermal histories in the glass transition range is explored, largely in terms of Kovacs' experimental data and attendant computations. These considerations are presented from a unified point of view of nonlinear thermoviscoelastic constitutive behavior, principally with phenomenological material description in mind. These computations provide guidance to the design of experiments for the proper determination of the relevant material functions and seem to indicate a need for the reevaluation of certain experimental procedures in the time histories of thermal material characterization.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pen.760270113
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  • 9
    Electronic Resource
    Electronic Resource
    Chemical reactions and temperature-dependent interface formation of Ti/InP (110)Paper presented at the Quantitative Surface Analysis (QSA-5) Conference, London, 15-18 November 1988. (1989)
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 14 (1989), S. 315-324 
    Details
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The reaction of a clean InP(110) surface with thin layers of titanium, deposited at room temperature and 140 K, was studied by core- and valence-level photoemission. We were able to identify reacted interface species by means of curve-resolving of high-resolution core-level spectra. It was found that titanium reacts strongly with InP(110), leading to a reacted layer of ∼9-12 Å thickness, which consists of a TiP compound. In this process, indium is liberated from the substrate and forms metallic islands in the surface region. Further deposition leads to the formation of a metallic Ti film, into which the indium is alloyed. On the basis of annealing experiments, we were able to identify the reacted zone as a diffusion barrier for further interface reaction. The reacted zone was found to broaden at elevated temperature. Our data are discussed with respect to studies of other transition metals with InP(110) and III-V semiconductor surfaces.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/sia.740140608
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  • 10
    Electronic Resource
    Electronic Resource
    The radical initiation of vinyl polymerization by α.α.α′.α′-Tetrasubstituted dibenzyls (1972)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 157 (1972), S. 279-298 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Im Temperaturbereich von 60 bis 100°C wird die radikalische Polymerisation von Styrol, Methylmethacrylat und Acrylnitril von α.α′-Dicyanodibenzylen ausgelöst, die in α-und α′-Stellung mit Ester-, Nitril-, Amid- oder Phenylgruppen disubstituiert sind. Bei 100 bis 110°C ist auch das α.α.α′.α′-Tetracarboxymethyldibenzyl aktiv. Vinylacetat und Vinylchlorid werden durch diese Initiatoren kaum polymerisiert.Fur die Polymerisation des Styrols wurden die Bruttogeschwindigkeitskonstanten Kp, für viele Dibenzyle und fur Peroxide vergleichbarer Aktivitat dilatornetrisch bestirnrnt. Norrnalerweise sind die Zeit-Urnsatz-Kurven rnit den Dibenzylen und den Peroxiden vergleichbar; das Tetracyanodibenzyl allerdings bewirkt nur eine unvollstandige Polymerisation.Der große Einfiuß von Substituenten in α-Stellung oder in den Phenylringen der Dibenzyle auf die Polymerisation des Styrols wird diskutiert. Dabei ist auch die Stereochernie wichtig. Die meso-Form des Dinitrildiesters ergibt eine 2.5- bis 3.5 ma1 schnellere Polyrnerisation als das dl-Isornere.Die Dissoziationsgeschwindigkeitskonstanten kd der Initiatoren wurden NMR-spektroskopisch aus der Linienbreite bestirnmt. Die Dinitrildiester sind gute Initiatoren, wahrend die α.α′-Dicyanodibenzyle rnit weiteren Nitril- oder Phenylgruppen in α- und α′-Stellung wenig geeignet sind. SchlieBlich wurde die 1.2-Addition einiger der Dibenzyle an Styrol im Ternperaturbereich von 120 bis 150°C rnit der Methode der chernisch induzierten KernPolarisation (CIDNP) untersucht.
    Notes: The radical polymerization of styrene, methyl methacrylate and acrylonitrile is initiated by α.α′-dicyanodibenzyls α.α′-disubstituted with ester, nitrile, amide or phenyl groups in the temperature range 60 to 100°C and by α.α.α′.α′-tetracarboxymethyldibenzyl at 100 to 110°C. Vinylacetate and vinylchloride show a low reactivity.The overall polymerization rate constants Kp have been determined dilatometrically for styrene initiated by a large number of dibenzyls and comparable peroxides. The styrene polymerization curves are generally comparable with those of peroxides. A notable exception is tetracyanodibenzyl.The strong influence of α- and ring-substituents in the dibenzyls on the styrene polymerization rate is discussed. The stereochemistry is also important : the meso α.α′-dicyanodibenzyls α.α′-disubstituted with ester groups give a 2.5 to 3.5 fold faster polymerization than their dl isomers.The initiator efficiency is related to the kd values, determined from NMR line width measurements. The α.α′- dicyanodibenzyls α.α′-disubstituted with ester groups are good initiators, while those with phenyl groups and nitrile groups are inefficient.Relevant to initiation and termination, the 1.2-addition of some of the dimers to styrene at 120 to 150°C has been studied with chemically induced dynamic nuclear polarization (CIDNP).
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1972.021570128
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