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  • 1
    ISSN: 1520-5827
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1536
    Keywords: Key words Alkyl maleates ammonium derivatives ; surfactants ; 1H NMR ; CMC ; emulsion polymerization
    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  The synthesis of several ammonium derivatives of maleic acid diesters are reported. The starting material is the hemiester of maleic acid, easily obtained from ring opening of the maleic anhydride. The hemiester is submitted to functionalization with an aminated compound, followed by quaternari-zation with the convenient alkylation reagent. Products crystallize easily and yields are generally high. They have been fully characterized by 1H and 13C NMR and the CMC have been measured. Some of them have been engaged in emulsion polymerization with styrene or methyl methacrylate. Maleates functionalized with quaternary ammonium salts yield polystyrene particle sizes around 30 nm with a narrow size distribution without adding any additional emulsifier.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1435-1536
    Keywords: Key words Characterization ; particle size distribution ; multi-sized ; latex ; centrifuge ; quasielastic light scattering
    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  A method for characterizing the particle size and size distribution of multi-sized polymer lattices was developed by combining quasielastic light scattering (QELS) with a centrifuge. Lattices were first fractionated by centrifugation and the different populations of particles were separated in successive steps. The size of these particles was measured by QELS, and the mass fraction of the particles was determined gravimetrically. The particle size and size distribution of several blends of monodisperse lattices and two industrial multi-sized lattices have been measured by this method. The results show that the particle sizes obtained using this method are in good agreement with the expected particle diameters, and that the relative amounts of the different groups of particles in the blends can be accurately determined. The efficiency of centrifuge-QELS was also confirmed by comparison with other techniques such as transmission electron microscopy (TEM), QELS, field-flow fractionation (FFF) and capillary hydrodynamic fractionation (CHDF). However, this method is not suited for the analysis of continuous, broad distributions or mixtures with a high number of different populations. It is better suited for distributions with a small number of families of particles, and then can be used for preparative propose on a laboratory scale.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1436-2449
    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: Summary Free radical homo- and copolymerisations of vinyl acetate and butyl acrylate were carried out in solution. Initial differences in data from homopolymerisation experiments lead us to investigate the influence of an eventual oxygen inhibition on the observed rate of polymerisation. A kinetic study at 70 °C was carried out both with and without a nitrogen purge. A decrease in the rate of polymerisation in the second instance was attributed to the presence of dissolved oxygen in the solution. Estimates of the apparent inhibition constant from different experiments are used to model both homopolymerisation and copolymerisation with vinyl acetate. The importance of taking this phenomenon into account during kinetic studies is demonstrated.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 255 (1977), S. 713-714 
    ISSN: 1435-1536
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1435-1536
    Keywords: Emulsionpolymerization ; emulsifier-freeconditions ; cationicinitiator ; poly-vinylbenzylchloride ; poly-vinylbenzyltrimethylammoniumchloride
    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 Polycationic polymers have been obtained through a two-step procedure. First, poly-vinylbenzylchloride [P(VBC)] latexes were prepared under emulsifier-free conditions using a cationic initiator: 2,2′-azobis(2-amidinopropane) hydrochloride; then the resulting latexes were reacted with trimethylamine. Particular attention was paid to side reactions occurring during the hydrolysis of the chloromethyl groups and the crosslinking reaction due to a transfer reaction onto polymer. The influence of various parameters on the particle size and structure of latexes as well as secondary reactions were investigated through a careful characterization.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 273 (1995), S. 984-993 
    ISSN: 1435-1536
    Keywords: Polymer adsorption ; flocculation ; bridging ; zeta potential ; colloidal particles
    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 Studies of the adsorption of high molecular weight polymers on colloidal latex and silica particles and their subsequent flocculation were carried out. Neutral polyethylene oxide samples with both a narrow and a broad molecular weight distribution were used together with low charged cationic copolymers. The influence of the particle concentration and polymer dose on the flocculation were systematically investigated under quiescent conditions. Equilibrium bridging only occurred with polyelectrolyte, even in very dilute suspensions, at high particle coverage. In contrast to this, non-equilibrium bridging occurred with both neutral polymer and polyelectrolytes but only for more concentrated suspensions and small amounts of adsorbed polymer. Polymer adsorption in dilute suspensions, which did not show particle aggregation was measured an electrophoretic technique. In more concentrated suspensions, where flocculation takes place, we found that aggregation prevents further polymer adsorption and induces both an excluded volume and a surface effect. The consequences on the shape of the isotherms differ according to the aggregation mechanism. A significant decrease of the amount, Γ, of adsorbed polymer is observed with non-equilibrium bridging. When both mechanisms simultaneously contribute to the aggregation, the value of Γ depends on their relative importance. In the intermediate range of copolymer dose their respective contributions are critically sensitive to the details of the mixing step and stirring, leading to non reproducible experimental results.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 270 (1992), S. 806-821 
    ISSN: 1435-1536
    Keywords: Latexparticles ; latexfilms ; coalescence ; smallangleneutronscattering
    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 The coalescence of latex particles is investigated through small-angle neutron scattering and electron microscopy. The particles are made of a soft polymeric core protected by a hydrophilic membrane, and they are dispersed in water. This dispersion is spread on a substrate, and water is removed to form a dry film. As the membranes of neighboring particles come into contact, they may break up to allow fusion of the particle cores. This is found to occur when the membranes are made of short-chain surfactant molecules; then all hydrophilic material is expelled to the film surface or to large isolated lumps. Alternatively, the membranes may remain until the film is completely dry; this is found to occur when they are made of hydrophilic polymers which are grafted onto the core. Hence, the fusion of particles is controlled by the connectivity of membranes.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 10 (1985), S. 199-214 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Inverse emulsion copolymerization studies of acrylamide (Am) with methacrylic acid (MAA) are reported. Aqueous monomer emulsions in toluene were prepared with a blend of two surfactants (sorbitan sesquioleate - Cl8 - terminated acrylamide oligomers). Polymerization kinetics in presence of an oil soluble initiator (AIBN) were determined at 40°C as function of MAA content and aqueous phase pH : monomer reactivity ratios have been derived as rAm = 0.58 ± 0.02, rMAA = 4.40 ± 0.10 at pH 4 and rAm = 0.56 ± 0.005, rMAA = 0.15 ± 0.03 at pH 10. Particle size and stability of inverse monomer emulsions and final latexes were found to depend upon the aqueous phase pH, as well as the intrinsic viscosities of the copolymers; this suggests differences in polymerization mechanism versus the pH.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 1127-1161 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Inverse emulsion copolymerization studies of acrylamide (Am) with methacrylic acid (MAA) are reported. Aqueous monomer solutions were emulsified in toluene with a blend of two surfactants (sorbitan sesquioleate and C18-terminated acrylamide oligomers). Polymerization kinetics in presence of an oil-soluble initiator (AIBN) were determined at 40°C as a function of methacrylic acid content and aqueous-phase pH. Polymerization rates were found to be faster at basic pH than at acidic pH, which appeared to be related to the actual concentration of methacrylic acid in the aqueous phase. Monomer reactivity ratios have been derived as rA-M = 0.58 ± 0.02 and rM-A = 4.0 ± 0.10 at pH 4, rA-M = 0.56 ± 0.005 and rM-A = 0.15 ± 0.03 at pH 10. These differences were found to have an effect on the molecular characteristics of the copolymers. Initial emulsions and final inverse latexes displayed the same broad size distribution; under basic pH the particle size is relatively insensitive to the ionic comonomer concentration. Poor latex stability is characteristic of copolymer latexes prepared under acidic conditions. Based on these experimental results, some aspects of the polymerization mechanism are discussed.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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