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  • 1
    Electronic Resource
    Electronic Resource
    Mechanism of accelerated photofading of thioether anthraquinone dyes in styrene butadiene resinsPresented, in part, at the IUPAC Photochemistry Symposium at Interlaken, Switzerland, July 1984. (1988)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 36 (1988), S. 1205-1219 
    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: Many anthraquinone dyes fade in visible light up to 100 times faster in styrene butadiene copolymers than in polyester resins or polystyrene. A mechanistic investigation of the photofading of 1,5-dihydroxy-2,6-diisobutyl-4-thiophenylanthraquinone has established that the dye sensitizes formation of singlet oxygen, a very reactive species, which attacks the double bonds in the styrene butadiene, resulting in extensive chain cleavage and peroxide formation. The major process is the oxidation of the polymer, and the dye fading is a minor process whereby the dye is apparently attacked by polymeric peroxides. The mechanism appears to be general for anthraquinone dyes, especially those with thioether, amino, hydroxy, or double-bond functionality. Unfortunately the fading is unaffected by most anticxidant stabilizers: the best result achieved was a doubling of half-life with 1 wt% Spinuvex A-36. This is still insufficient to give colored styrene butadiene copolymer resins the intrinsic dye stability available in other polymers, rendering styrene butadiene unsuitable for applications requiring high photostability of anthraquinone dyes.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1988.070360520
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  • 2
    Electronic Resource
    Electronic Resource
    The controlled flocculation of submicron emulsion particles. I. A three-step synthetic route to supermicron polymer particles (1996)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 3061-3069 
    Details
    ISSN: 0887-624X
    Keywords: aggregation ; emulusion polymerization ; flocculation ; latex ; particles ; polymer ; size distribution ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The basic features of a three-step experimental process to produce supermicron polymer particles are described. First, a submicron emulsifier-free latex is prepared by a well-known technique. Second, the latex is aggregated by destabilizing with cetyl pyridinium chloride under constant stirring conditions, to yield roughly spherical clusters of 6-12 μ diameter. Third, the aggregates are stabilized with poly(vinyl alcohol) and internally coalesced by heating at or above the glass transition temperature. The final product particles have relatively smooth surfaces. Results are qualitatively interpreted in terms of a dynamic equilibrium where the aggregate size is determined by a balance between attractive interparticle potentials and stirring shear forces. Bimodal aggregate size distributions suggest the aggregate break-up mechanism may involve the erosion of individual latex particles and small fragments from the surface of aggregates. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1996.866
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  • 3
    Electronic Resource
    Electronic Resource
    Dispersion polymerization of styrene in polar solvents. IV. Solvency control of particle size from hydroxypropyl cellulose stabilized polymerizationsPresented in part at the Canadian High Polymer Forum, Ottawa, August, 1987, and the NATO ASI on Polymer Colloids, Strasbourg, July, 1988; for Paper I of this series, see Ref. 1 (1990)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2485-2500 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Changing solvent has a dramatic effect on the outcome of HPC stabilized dispersion polymerization of styrene in polar solvents. In methoxyethanol/ethanol mixtures, particle size varies from essentially infinity for unstabilized reactions (below 30% ethanol) to about 3 microns in ethanol. In a series of n-alcohols, there was a maximum in particle size at intermediate chain length: particle size increased from 2 microns in methanol to 8.3 microns in pentanol, then decreased again to 1 micron in octadecanol. These results were rationalized in terms of the three-component Hansen solubility parameters. The largest particles were obtained in solvents with Hanson polarity and hydrogen bonding terms closest to HPC. The generality of the three-component solubility parameter approach was examined by reactions performed in eight mixed solvents with the same values of all three Hansen terms. Seven of the eight solvents gave particles of similar size and molecular weight. The two critical effects of solvent on both particle size and molecular weight appear to be: (a) the solubility properties of the grafted HPC-PS formed, and (b) the partitioning of monomer and initiator between solution and particle phases subsequent to nucleation.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1990.080280921
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  • 4
    Electronic Resource
    Electronic Resource
    Control of surfactant level in starve-fed emulsion polymerization. I. Sulfate-containing oligomers: Preparation and application as surfactant in emulsion polymerization (1995)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 1597-1606 
    Details
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; surfactants ; oligomers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is well known that the amount of surfactant must be carefully controlled during starve-fed emulsion polymerization processes. Too little surfactant leads to emulsion instability and coagulation, while too much surfactant leads to secondary particle formation. Although these relationships are qualitatively understood in the art, there is little quantitative basis to guide the synthetic chemist, especially in multistep starve-fed emulsion polymerization processes to make larger supermicron particles. We have developed a method, which will be described in a companion article, to control the surfactant level by monitoring the surface tension during polymerization. In order to quantitatively predict how much surfactant to add at any given time, one needs to know in advance the adsorption characteristics of the soap. Further complicating the matter is the formation of “in situ” or oligomeric surfactant during polymerization with aqueous initiators such as ammonium persulfate.This work demonstrates how to prepare surface-active oligomers and how to make latex particles using them as surfactant. First, we established the mass balance for the initiator-derived sulfate groups in seed latexes by conductometric, potentiometric, and iodometric titrations. Based on the characterization of seed latexes, a method for determining the effective sulfate concentration has been developed. When surface-active oligomers were used as the only surfactant, we obtained a series of monodisperse, supermicron copolymer latex particles with diameters up to 3.22 μm. This is a similar result to that obtained with a commercially made anionic surfactant. © 1995 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1995.080331006
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  • 5
    Electronic Resource
    Electronic Resource
    An application of arene-iron chemistry in the synthesis of a novel liquid crystalline polymer (1997)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 447-453 
    Details
    ISSN: 0887-624X
    Keywords: polyether ; polyester ; aryl ether ; nucleophilic substitution ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arene-iron chemistry was applied in the synthesis of a novel liquid crystalline polymer. The chemistry, which is based on iron cyclopentadienyl (FeCp) arene complexes, allows sequential nucleophilic substitution of the chlorides from 1,3-dichlorobenzene-FeCp complex and photolytic decomplexation of the products to afford asymmetrical aryl ethers. This methodology provides easy access to novel polyether-esters, and is potentially useful in the synthesis of various functional polyarylates. © 1997 John Wiley & Sons, Inc.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    A comment on the paper “uniform polymer particles by dispersion polymerization in alcohol,” by C. M. Tseng, Y. Y. Lu, M. S. El-Aasser, and J. W. Vanderhoff [J. polym. sci. polym. chem. Ed. 24, 2995 (1986)]Presented, in part, at the NATO ASI on Polymer Colloids (Strasbourg, July 1988). This is Paper 5 in a series including Refs. 5-8 (1990)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2569-2574 
    Details
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1990.080280928
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  • 7
    Electronic Resource
    Electronic Resource
    Use of 13C tags with specifically 15N-labeled DNA and RNA (1998)
    New York : Wiley-Blackwell
    Biopolymers 48 (1998), S. 57-63 
    Details
    ISSN: 0006-3525
    Keywords: 15N-nmr ; 13C-nmr ; specific labeling ; 13C tags ; nucleoside synthesis ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We describe methods to introduce 13C specifically to the C2 or C8 positions of 15N-multilabeled purines, thereby permitting “13C tagging” of all base nitrogens except the amino group of adenosine. These procedures permit the incorporation of two or more 15N-multilabeled monomers into a given DNA or RNA fragment, with and without appropriate 13C tags. This approach increases the number of 15N-nmr resonances that can be unambiguously distinguished and thus the amount of information from a single synthesis and a single nmr experiment. © 1998 John Wiley & Sons, Inc. Biopoly 48: 57-63, 1998
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Configuration biased Monte Carlo and Brownian dynamics simulations of semiflexible polymers in extensional flows (1998)
    Weinheim : Wiley-Blackwell
    Macromolecular Theory and Simulations 7 (1998), S. 19-26 
    Details
    ISSN: 1022-1344
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Configuration Biased Monte Carlo (CBMC) and Non-Equilibrium Brownian Dynamics (NEBD) simulations are used to understand the dynamics of semi-flexible macromolecules undergoing extensional flow. The mathematical model utilizes a discretized version of the Kratky-Porod wormlike (or persistent) chain as the building block, and using kinetic theory, generalized to include flow. In steady, potential flows, the solution of the Fokker-Planck equation exists and is used in the generation of trial and acceptance moves in the CBMC scheme. For the NEBD, the Fokker-Planck equation is converted to a Stochastic Differential Equation (SDE) from which the simulation algorithm is obtained. Various conformational quantities are monitored, under both steady-state and transient conditions, with the primary independent variable being the flexibility parameter β, the bending constant of the chain. It is found that the model is able to describe qualitatively many of the experimentally observed effects in such systems. In particular, we find that there is a direct link between the molecular flexibility and its birefringence response in an elongational flow field. We are able to draw conclusions by considering the behavior of molecular-conformational quantities such as the radius of gyration and the moment of inertia.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Reactive diluents and properties of ultraviolet-cured polycarbonate urethane acrylates (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 57 (1995), S. 1627-1636 
    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: Polymer films obtained from photocurable formulations were investigated by tensile methods and dynamic mechanical analysis. The polymer formulations contained photoinitiator, urethane diacrylate oligomer, and acrylic reactive diluent. It was found that diluent concentration may strongly affect the glass transition temperature and elastic modulus of the cured coating. When the diluent homopolymer glass transition temperature is larger than that of oligomer homopolymer, the glass transition temperature and elastic modulus of the coating film increase with the increase of the diluent concentration. When the diluent homopolymer has lower glass transition temperature than the homopolymer of the oligomer, the increase in diluent concentration leads to a decrease in glass transition temperature and elastic modulus of the UV-cured coating film. The effect of the testing temperature on tensile storage modulus of the films containing different concentrations of reactive diluents was studied as well. The data indicated that a variety of coatings with wide ranging but predictable properties can be formulated from previously examined starting materials but used at different concentrations. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1995.070571309
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  • 10
    Electronic Resource
    Electronic Resource
    Urea hard segment morphology in flexible polyurethane foam (1998)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 573-581 
    Details
    ISSN: 0887-6266
    Keywords: polyether polyol ; polyurethane foam ; block-segmented copolymers ; microphase separation ; optical microscopy ; transmission electron microscopy ; small-angle X-ray scattering ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of flexible polyurethane slabstock foam samples were prepared with varying water content and studied using transmission electron microscopy (TEM), video-enhanced optical microscopy (VEM), and small-angle X-ray scattering (SAXS). A new TEM sample preparation technique was developed in which the foam is impregnated with water, frozen, and microtomed, and the polyether soft segment is selectively degraded in the electron beam. Structures of two size scales were detected. A texture with grains (“urea aggregates”) 50-200 nm in size was imaged using both VEM and low-magnification TEM for foams with formulations containing more than 2 pphp water. For the first time, images of urea hard segment microdomains in polyurethane foam (approximately 5 nm in size) were obtained using high-magnification TEM. A microdomain spacing of approximately 6-8 nm was estimated from the SAXS scattering profiles. Glycerol was added to one of the formulations in order to modify the urea microphase separation and to give insight into morphology development in molded polyurethane foam systems. No structure was observed in low-magnification TEM images of the glycerol-modified foam, although smaller structures (hard segments) were detected at high magnification and by SAXS. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 573-581, 1998
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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