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  • 1
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 81 (1998), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A homogeneous and stable amorphous-type cordierite (2MgO2Al2O35SiO2) powder was prepared by a solution-polymerization route employing a Pechini resin or a poly(vinyl alcohol) (PVA) solution as the polymeric carrier. After calcination at 800°C for 1 h under atmospheric conditions, the bulky precursor changed into a very soft and porous powder. A 30 nm size, amorphous-type cordierite powder was prepared by attrition milling the calcined powder, which was made using a PVA precursor solution. The nano-size powder, which had a high specific surface area of 181 m2/g, was obtained after milling for 〈1 h. The sintered cordierite grains did not show the presence of any amorphous SiO2 phase and had a dense microstructure with a relative density of 99% and a thermal expansion coefficient of 2.1 10-6/°C.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 55 (1990), S. 4544-4549 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 80 (1997), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Alumina–glass composites that contain oxidized aluminum were investigated to make shrinkage-free, all-ceramic dental porcelain. This was achieved by control of the volume expansion and shrinkage that occur during the aluminum oxidation and densification processes. The dimensional change and strength of the alumina-glass composites were dependent on the aluminum content and particle size. A shrinkage-free sample with a strength of 330 MPa and transmittance of 1.21 was fabricated by using 4-5 vol% of aluminum powder with an average particle size of 6 μ m in the alumina-glass composite made by the In-Ceram method.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    Journal of the American Ceramic Society 88 (2005), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: An interesting concept for achieving graceful failure in oxide composites is discussed. It is based on crack deflection in a weak interphase between a matrix and reinforcement (e.g. fiber), around a fibrous core in a fibrous monolith, or in an interphase in a laminated composite. The interphase can be phase transformation weakened by a crystallographic unit cell, volume contraction, and/or shape change. Mullite/cordierite laminates with a β→α-cristobalite, transformation-weakened interphase were investigated for interphase debonding behavior. The laminates were fabricated by stacking alternate, tape-cast, green sheets of chemically doped β-cristobalite, which was synthesized by an organic steric entrapment method, and a mullite/cordierite matrix mixture. The laminate showed fracture behavior depending on a critical particle size effect. The grain size of polycrystalline β-cristobalite was controlled by annealing time at 1300°C. A hot-pressed laminated composite, annealed for 10 h at 1300°C, had an average grain size of ∼4 μm and a 3-point flexure strength of 131 MPa. Its work of fracture was 2.4 kJ/m2 but non-catastrophic fracture behavior was demonstrated. The indentation response indicated crack deflection along the cristobalite debonding interphase. With increasing annealing time, the strength decreased due to the formation of internal macrocracks in the cristobalite layer, which occurred spontaneously during thermally induced transformation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 84 (2001), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A novel mechanism for debonding at a weak interphase in an all-oxide composite is introduced. This methodology involves the use of alumina platelets that have a diameter of 10–15 or 5–10 μm and a thickness of 1 μm. The platelets induce constrained sintering of the ceramic powder, which results in permanent porosity. For room-temperature properties, only minor additions (0–3 vol%) of matrix powder yield sufficiently weak debonding interphases. The platelets lie in random, three-dimensional orientations and provide a debonding mechanism that is independent of temperature, in chemically compatible matrixes. Laminated composites with two types of matrixes—mullite and alumina—have been fabricated with modified fibrous monoliths of alumina in a triple-layer “core/interphase/matrix” arrangement. In the laminated systems, the intimate mixing of strong versus tough microstructures has been tailored by alternating various matrix:interphase thickness ratios. Preliminary load–displacement curves clearly demonstrate characteristics of “graceful failure” and notable improvements in the work of fracture. Scanning electron microscopic observation of the crack paths confirms the viability of platelets for producing permanently porous, debondable interphases at elevated temperatures in air.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Westerville, Ohio : American Ceramics Society
    Journal of the American Ceramic Society 82 (1999), S. 0 
    ISSN: 1551-2916
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The four components portland cement-dicalcium silicate, C2S (Ca2SiO4); tricalcium silicate, C3S (Ca3SiO5); tricalcium aluminate, C3A (Ca3Al2O6); and tetracalcium aluminate iron oxide, C4AF (Ca4Al2Fe3O10)-were formed using a solution-polymerization route based on poly(vinyl alcohol) (PVA) as the polymer carrier. The powders were characterized using X-ray diffraction techniques, BET specific surface area measurements, and scanning electron microscopy. This method produced relatively pure, synthetic cement components of submicrometer or nanometer crystallite dimensions, high specific surface areas, as well as extremely high reactivity at relatively low calcining temperatures. The PVA content and its degree of polymerization had a significant influence on the homogeneity of the final powders. Two types of degree of polymerization (DP) PVA were used. Lower crystallization temperatures and smaller particle size powders were obtained from the low-DP-type PVA at optimum content.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Solid state phenomena Vol. 119 (Jan. 2007), p. 43-46 
    ISSN: 1662-9779
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Physics
    Notes: Nano scaled mullite (3Al2O3·2SiO2) powders had been fabricated by anorganic-inorganic solution technique using a polyvinyl alcohol (PVA) as an organic carrier.PVA polymer contributed to a soft and porous powder microstructure, and ball milling with theporous powder was effective in making nano-sized mullite powders. In addition, the degree ofpolymerization of PVA affected the crystallization behavior. The fully crystallized and ball-milledmullite powders had an average particle size of 120 nm with a specific surface area of 67.0m2/g. In this paper, the simple solution technique and milling process for the fabrication of nanoscaled mullite powders are introduced. And the effects of PVA on the crystallization behavior andpowder specific surface area are also studied. The characteristics of the synthesized powders areexamined by using XRD, TEM, particle size analyzer and nitrogen gas adsorption
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Solid state phenomena Vol. 124-126 (June 2007), p. 807-810 
    ISSN: 1662-9779
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Physics
    Notes: Highly sinterable lithium titanate (Li2TiO3) powder was fabricated by an organic-inorganicsolution route. Liquid-type ethylene glycol (EG) was used as an organic carrier for the metal cations.Titanium isopropoxide and lithium nitrate were dissolved in the liquid-type ethylene glycol withoutany precipitation. The dried precursor gel showed crystalline form at 300 °C and carbon-free Li2TiO3was observed above 400 °C. The primary particle size of the carbon-free Li2TiO3 was about 100 nm,and the structure of the crystallized powder was porous and agglomerated. The porous powder wasball-milled and easily ground to fine particles. The powder compact was densified to 93% theoreticaldensity (TD) at relatively low sintering temperature of 1100 °C for 2 h. The densifed Li2TiO3 showeda small grain size of 1.2 μm. As well, the grain size was notably increased at 1200 °C and above. Afterthe over grain growth, further densification was no more observed
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-2013
    Keywords: Redox ; NADH ; Reduced glutathione ; 5,5′-Dithio-bis(2-nitrobenzoic acid) ; Ca-activated K channel ; Pulmonary arterial smooth muscle cell ; Hypoxic pulmonary vasoconstriction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Astract We investigated the electrical responses of Ca-activated K (KCa) currents induced by hypoxia and reduction or oxidation of the channel protein in pulmonary (PASMC) and ear (EASMC) arterial smooth muscle cells using the patch-clamp technique. In cell-attached patches, in the presence of a high K solution (containing 0.316 (μM Ca2+), the activity of KCa channels from PASMC was decreased (by 49±7% compared to control, pipette potential = −70 mV) by changing to a hypoxic solution (1 mM Na2S2O4, aeration with 100% N2 gas). EASMC channels did not respond to hypoxia. In order to investigate the possible mechanisms involved, using inside-out patches bathed symmetrically in 150 mM KCl, we applied redox couples to the intracellular side. Reducing agents, such as dithiothreitol (DDT, 5 mM), reduced glutathione, (GSH, 5 mM), and nicotinamide adenine dinucleotide reduced (NADH, 2 mM) decreased PASMC, but not EASMC, KCa channel activity. However, oxidizing agents such as 5,5′-dithio-bis(2-nitrobenzoic acid) (DTNB, 1 mM), oxidized glutathione (GSSG, 5 mM) and NAD (2 mM) increased KCa channel activity in both PASMC and EASMC. The increased activity due to oxidizing agents was restored by applying reducing agents. From these results, we could suggest that the basal redox state of the EASMC KCa channel is more reduced than that of the PASMC channel, since the response of KCa channels of the EASMC to intracellular reducing agents differs from that of the PASMC. This difference may be related to the different responses of PASMC and EASMC KCa channels to hypoxia.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 62 (1996), S. 1011-1021 
    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: UV-curable polyurethane acrylates for poly(vinyl chloride) (PVC) floor coating were prepared using nonyellowing polyisocyanates. The effects of the chemical structure of the polyisocyanates and hydroxyacrylates, and the compositions of the prepolymer/diluent on the properties of the UV-curable polyurethane acrylates were investigated. Several different urethane acrylate prepolymers from four different polyisocyanates, isophorone diisocyanate (IPDI) adduct, hexamethylene diisocyanate (HDI) adduct, HDI biuret, and HDI isocyanurate, and two different hydroxyacrylates, hydroxyapropyl acrylate (HPA), polycaprolactone modified hydroxyethylhexylacrylate (PCMHEA). UV-curable coating materials were formulated from the prepolymers and 1-hydroxycyclohexylphenyl ketone as a photoinitiator with polyethylene glycol diacrylate (PEGDA) as a diluent. The polyurethane acrylates prepared with HDI isocyanurate and the equimolar mixture of HPA and PCMHEA showed balanced coating properties such as tensile properties, hardness, weatherability, and good adhesion. The dynamic mechanical studies showed the properties of those polyurethane acrylates were well correlated with their glass transition temperature behaviors. It was also found that the adhesion was best as a PVC floor coating with the appropriate viscosity (below 150 P at 25°C) when 35% PEGDA as a diluent was used. © 1996 John Wiley & Sons, Inc.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
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