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  • 1
    ISSN: 1436-3771
    Keywords: Key words Composite resins ; Polymerization ; Marginal adaptation ; Light intensity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The aim of this study was to evaluate the effect of a rapid photopolymerization method on the marginal integrity of composite fillings. Ninety two-surface cavities were prepared in extracted human molars using the SonicSys preparation system. All cavities were bonded with one bonding agent (Syntac) and filled with a microfilled composite (Herculite XRV), a heavy filled composite (Z100 MP), and an Ormocer (Definite) in two increments. Each increment had a thickness of approximately 1.5 mm and was polymerized using either halogen light or the plasma light of Apollo 95 E. In this process, six trial groups each containing 15 fillings were created. After replicas were made, the test teeth were subjected to a thermocycling process of 2000 temperature cycles (5°C/55°C) followed by a wear simulation of 50,000 stress cycles each with 50 N. This was followed by the creation of a second set of replicas, quantitative margin analysis, and dye penetration. A significant (P〈0.05) influence of the thermomechanical stress and a significant (P〈0.05) influence of the factor ”material” were shown for the margin criterion ”continuous margin” using MANOVA. The factor ”light source” produced no significant influence (P=0.57) on the amount of continuous margin. During the dye penetration, no significant differences between the polymerization methods could be established with the materials Herculite XRV and Z100 MP (H-test according to Kruskall and Wallis). Only with the material Definite was a significantly higher dye penetration observed at the occlusal measuring point in the plasma light group. A rapid polymerization with high light intensity had no adverse effects on the margin quality within the limitations of this in vitro study. However the marginal integrity might have been influenced by the chosen adhesive system/composite resin combination, which does not represent the respective product line. Additionally, further studies ought to show which exposure time is necessary for a sufficient degree of conversion.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-8935
    Keywords: Functional monomers ; Polymerization ; Copolymerization ; Kinetic studies ; Reactivity ratios
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract 1-Cyanoethanoyl-4-acryloylthiosemicarbazide (CEATS) was synthesized for the first time as a new chelating monomer. Its structure was confirmed by both elemental and spectral analyses. Radical polymerization and copolymerization of CEATS was been carried out in dimethylformamide (DMF) in the presence of azobisisobutyronitrile (AIBN) as an initiator. Kinetic studies for the polymerization behavior of CEATS were performed. The complex formation of the CEATS monomer and polymer (PCEATS) with Cu II cation was investigated and its stability constant determined. The rate of copolymerization of CEATS with some conventional monomers, namely vinyl acetate, methyl methacrylate and acrylonitrile, was measured as a function of the mole fraction of the monomers. The reactivity ratios (r1, r2) for the various copolymer systems investigated together with the Q and e values of the CEATS monomer were determined. Moreover, the thermal gravimetric analysis of the prepared polymers and their copolymers with acrylonitrile were also studied.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of wood science 46 (2000), S. 143-148 
    ISSN: 1611-4663
    Keywords: α-Pinene ; Phenol ; Formaldehyde ; Polymerization ; Condensation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Synthesis conditions of terpene-phenol-aldehyde resin with a high softening point were studied based on the reactions amongα-pinene, phenol, and formaldehyde. A suitable catalyst system and the best processing conditions were obtained by laboratory experiments. The influence of the raw materials ratios, reaction temperature, reaction time, and catalyst dose on the softening point, yield, and color of the synthesized resin was examined. The physical and chemical characteristics of the resin were determined: softening point ≥140°C (ball and ring method); color value ≤7 (Gardner); acid value (KOH mg/g) 〈1; bromine value (Br2 mg/100g) 〈64; saponification value (KOH mg/g) 〈1; average molecular weight ∼830. The yield of resin was more than 85% (based on the total raw material).
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 278 (2000), S. 150-154 
    ISSN: 1435-1536
    Keywords: Key words Hydrolysis kinetics ; Polymerization ; Microemulsions ; Aspirin ; Styrene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Two kinds of chemical reactions were studied in two different microemulsion systems: cetyltrimethylammonium bromide/1-butanol/10 and 25% n-octane/water and sodium dodecyl sulfonate/1-butanol/20% styrene/water. One reaction is a hydrolysis reaction, in which aspirin and 2,4-dinitrochlorobenzene were used as the hydrolysis substrates. The second reaction is the polymerization of styrene, which was initiated by using two initiators, water-soluble K2S2O8 and oil-soluble 2,2′-azobis(isobutyronitrile), and, at the same time, the polymerization of acrylamide, which was initiated by NaHSO3, was also studied. All the hydrolysis reaction experimental results show that the hydrolysis is greatly affected by the structures and the structural transitions of microemulsions. The hydrolysis rates are higher in water-in-oil (W/O) microemulsion media and decrease with the addition of water. The rates increase in bicontinuous (BC) microemulsions and decrease in oil-in-water (O/W) microemulsions. The transition points of the hydrolysis rates occurred at the two microemulsion structural transition points from W/O to BC and from BC to O/W. The polymerization relationships between the conversions of styrene, the molecular weights of polystyrene and the water contents of the microemulsion system were obtained. The effects of microemulsion structures on the sizes of the polystyrene particles and on the molecular weights of the polymers are discussed. Polystyrene particles with diameters of 10–60 nm were observed by microscopy. Our experimental polymerization results show that microemulsions are suitable as media for the production of polymers, the molecular weights and the particle sizes of which can be controlled and predicted by variations in microemulsion structures.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1434-1948
    Keywords: Aluminum ; Alkoxides ; Lactone ; Ring-opening ; Polymerization ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of trialkylaluminum Al2R6 (R = Me, Et) with 2,2′-methylenebis(6-tert-butyl-4-methylphenol) (mbmpH2) gives the dimeric mono(alkyl) complex [Al(mbmp)R]2 with bridging oxygen atoms. Reaction of [Al(mbmp)R]2 with one equiv. of 2-propanol results in the formation of the dimeric isopropoxide [Al(mbmp)(μ-OiPr)]2. Single-crystal X-ray analysis shows a C2h-symmetric structure with a planar Al2O2 core. Monomeric methylbis(2,6-di-tert-butyl-4-methylphenolato)aluminum, AlMe(OC6H2-2,6-tBu2-4-Me)2 (MAD), was found to react with one equiv. of 2-propanol to give a dimeric isopropoxide [AlMe(OC6H2-2,6-tBu2-4-Me)(μ-OiPr)]2 in which the bulky phenolate, instead of the methyl group, has been displaced. According to the single-crystal X-ray structure analysis, the molecule contains a similar Al2O2 core, but the two 2,6-di-tert-butyl-4-methylphenolato ligands are cis- and orthogonally arranged to each other. ε-Caprolactone is polymerized at 50 °C in toluene in a controlled manner by [Al(mbmp)(μ-OiPr)]2, to give poly(ε-caprolactone) with high molecular weights and narrow molecular weight distributions (Mw/Mn 〈 1.50). The low efficiency values (number of polymer chains initiated per aluminum atom) imply that [Al(mbmp)(μ-OiPr)]2 exists in a monomer-dimer equilibrium. The polymerization of ε-caprolactone by [AlMe(OC6H2-2,6-tBu2-4-Me)(μ-OiPr)]2 is faster, but somewhat less controlled.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 38 (1994), S. 433-437 
    ISSN: 1432-1432
    Keywords: Aziridine ; Polymerization ; Template polymerization ; Oligonucleotide initiators ; Electrophoretic analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We have prepared a [32P]-labeled oligonucleotide probe carrying a free primary amine at its 3′terminus. This probe is used to initiate polymerization of aziridine (ethyleneimine) in aqueous solution. The nature of the oligomeric products and the kinetics of their formation are then monitored by gel electrophoresis. Our results are generally consistent with those obtained using conventional techniques. We have also investigated the effect of polyanionic templates on the rate of oligomerization of aziridine. We find that water-soluble polyanions generally accelerate the polymerization. The sodium salt of polymethacrylic acid is the most effective of the templates that we studied. The methods introduced in this paper should be applicable to a variety of polymerization reactions in aqueous solution. They should greatly simplify the screening of potentially prebiotic polymerization reactions.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 49 (1993), S. 110-117 
    ISSN: 1420-9071
    Keywords: Polymerization ; sickle hemoglobin ; sickle cell disease ; kinetics ; thermodynamics ; polymer domains ; nucleation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The polymerization of sickle hemoglobin occurs by the same mechanisms in solutions and in cells, and involves the formation of 14 stranded fibers from hemoglobin molecules which have assumed a deoxy quaternary structure. The fibers form via two types of highly concentration-dependent nucleation processes: homogeneous nucleation in solutions with hemoglobin activity above a critical activity, and heterogeneous nucleation in similarly supersaturated solutions which also contain hemoglobin polymers. The latter pathway is dominant, and creates polymer arrays called domains. The individual polymers bend, but also cross-link, and the resulting mass behaves as a solid. The concentration of polymerized hemoglobin increases exponentially unless clamped by rate limiting effects such as oxygen delivery.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1435-1536
    Keywords: Polymerization ; oligomerization ; norbornene ; PdCl2 catalysis in water ; emulsions ; latex ; 13C NMR ; tacticity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Polymerization of norbornene using PdCl2 as catalyst is generally carried out at high temperatures in the absence of solvent. Low yields of polymer with relatively undefined molecular weights are obtained under these conditions. We describe the first example of polymerization of norbornene in water dispersion or aqueous emulsions catalyzed by PdCl2. Good yields of polymers and oligomers were obtained. Furthermore, in aqueous emulsions, novel microlatex which cannot be obtained by radical or ionic routes were synthesized, with particles sizes (≈10 nm.) generally only observed in microemulsion polymerizations. The stereochemistry of the polymers of low molecular weight was partially elucidated by13C NMR.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-5133
    Keywords: Acidification ; Al-chemistry ; Speciation ; Polymerization ; Al-toxicity ; Freshwater fish
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Synopsis The present study focuses on the effect of temperature on Al-chemistry and the subsequent toxicity to smoltifying Atlantic salmon, Salmo salar. Fish were exposed to acidic Al-rich water at different temperatures, and mortality, ventilation frequency and various blood parameters were measured. The relationship between temperature and Al-toxicity was documented as mortality increased systematically with increasing temperature. Physiological disturbances at the gills reflected the temperature dependent Al-toxicity. The temperature dependent toxicity observed is probably due to the degree of ongoing Al-polymerization.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 4 (1993), S. 435-438 
    ISSN: 1042-7147
    Keywords: Ziegler-Natta ; Catalyst ; Polymerization ; Ethylene ; Styrene ; Copolymers ; 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
    Notes: The magnesium chloride supported Ziegler-Natta catalysts are able to copolymerize ethylene and styrene in conditions of high activity. Different parameters, including catalyst type, monomer ratio, temperature and Lewis bases, allow variation of the activity and reactivity ratio. The incorporation of styrene in the copolymer remains always rather limited in moles. The products obtained contain less than 20% styrene in weight, and seem very similar in structure to linear low-density polyethylenes (LLDPE) obtained with the same catalyst: the melting temperature is only about 5°C lower than that of pure polyethylene. The polymer can be fractionated by solvents in a similar manner to LLDPE, and contains a styrene-enriched fraction, but homopolystyrene production has never been observed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 11
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 4 (1993), S. 415-422 
    ISSN: 1042-7147
    Keywords: Polymerization ; Metallocenes ; Aluminoxane ; Metal-filled polymers ; 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
    Notes: Homogeneous catalysts based on metallocenes/methylaluminoxane are totally absorbed on surfaces of different metals. Because the methylaluminoxane is relatively stable against small molecules such as water covering metal surfaces, the aluminoxane can be fixed on powders without losing its activity. After treatment with the metallocene, active sites are only formed on the surface of the fillers. Upon injection of the olefins they are polymerized in the presence of the metals. Olefins such as ethene and propene, and cycloolefins or dienes, are used.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 4 (1993), S. 406-414 
    ISSN: 1042-7147
    Keywords: Polyolefin ; Polypropylene ; Polyethylene ; Catalyst ; Polymerization ; Process ; Elastomer ; 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
    Notes: The polyolefins, especially polypropylene and polyethylene, industry of today is very different from that of 10 years ago. The development of highly active and stereospecific catalysts, represented by Ti/Mg supported catalysts, have made the gas-phase polymerization process practical.The trend in catalyst development is shifting from an emphasis on improving the stereospecificity and activity toward improving the polymer physical properties, processability and morphology.Many hybrid thermoplastic olefins, such as high-impact copolymers, propylene-ethylene-butene terpolymers, and very low density polyethylene, have already been developed by utilizing the features of the gas-phase polymerization process.These hybrid thermoplastic olefins cover a very broad range of products. They cannot be clearly identified as polyethylenes, polypropylenes or elastomers.Incidentally, metallocene catalysts for polyolefins have been under development for the past 15 years, and are now in the early stage of commercialization. These catalysts differ significantly from the conventional heterogeneous catalysts.They can polymerize not only ethylene, propylene and other linear α-olefins, but also styrene, cycloolefins and functional monomers In addition, they can control the microstructure of polymer molecules by varying the transition metals and the cyclopentadienyl ligands.Because of these features, we have to be confident that the development of metallocene catalysts, or more widely homogeneous catalysts, may be a dominant force throughout the 1990s in the polyolefin industries.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    The astronomy and astrophysics review 3 (1991), S. 1-46 
    ISSN: 1432-0754
    Keywords: Nucleosynthesis ; Nuclear reactions ; Stars: abundances ; Interstellar Medium: abundances ; Cosmology ; Galaxies: evolution of
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Summary The basic scheme of nucleosynthesis (building of heavy elements from light ones) has held up very well since it was first proposed more than 30 years ago by E.M. Burbidge, G.R. Burbidge, A.G.W. Cameron, W.A. Fowler, and F. Hoyle. Significant advances in the intervening years include (a) observations of elemental and a few isotopic ratios in many more extrasolar-system sites, including metal-poor dwarf irregular galaxies, where very little has happened, and supernovae and their remnants, where a great deal has happened, (b) recognition of the early universe as good for making all the elements up to helium, (c) resolution of heavy element burning in stars into separate carbon, neon, oxygen, and silicon burning, with fine tuning of the resulting abundances by explosive nucleosynthesis in outgoing supernova shock waves, (d) clarification of the role of Type I supernovae, (e) concordance between elements produced in short-lived and long-lived stars with those that increased quickly and slowly over the history of the galaxy, and (f) calibration of calculations of the evolution and explosion of massive stars against the detailed observations of SN 1987A. The discussion presupposes a reader (a) with some prior knowledge of astronomy at the level of recognizing what is meant by an A star and an AGB star and (b) with at least a mild interest in how we got to where we currently are.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 2691-2695 
    ISSN: 0009-2940
    Keywords: fac-[Ru(O2CCH3)2(PPh3)3] · 2 CH3CO2H ; Tris(triphenylphosphane)ruthenium(II) ; Polymerization ; Bicyclo[2.2.1]hept-2-ene ; Ruthenium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [Ru2(μ-O2CCH3)4(O2CCH3)] reacts with excess triphenylphosphane in acetic acid to give fac-[Ru(O2CCH3)2(PPh3)3] · 2CH3CO2H (1), which crystallizes in the triclinic space group P 1- with Z=2. The three phosphane ligands are in the sterically congested facial configuration, and the distorted octahedral geometry around the metal is completed by a unidentate and chelating acetate. A variable temperature 31P{1H}-NMR study of the complex in CH2Cl2 showed the three phosphanes to be inequivalent at low temperature. On raising the temperature two separate coalescence processes are observed, ultimately making all of the phosphanes equivalent at room temperature. Complex 1 shows slight catalytic activity for the ring-opening polymerization of bicyclo[2.2.1]hept-2-ene (norbornene).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 2 (1991), S. 21-24 
    ISSN: 1042-7147
    Keywords: Polymerization ; Curing ; Laser ; Acrylic Monomer ; Ultraviolet Curing ; 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
    Notes: Photopolymerization of multifunctional acrylic monomers using excimer and Nd: YAG lasers operated at five different UV wavelengths is reported. The effects of different wavelengths on the surface and bulk cure both in air and under argon are investigated and discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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