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  • 1
    ISSN: 0006-3592
    Keywords: catalase ; photografting ; photosynthesized ; enzymatic membranes ; tangential flow ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Catalase has been immobilized within sandwich membranes prepared by the photoinduced grafting of an epoxy-diacrylate prepolymer onto commercial asymmetric cellulose membranes. The enzymatic activity of the membrane composite of hydrogen peroxide decomposition has been studied in a recirculation apparatus under tangential flow conditions without ultrafiltration. The enzymatic membranes were exposed to very low mechanical stresses and showed a very good catalytic performance and durability. Initial reaction rates, measured at 25°C as a function of both substrate concentration and enzyme amount immobilized per unit membrane surface, indicate that the mechanism of action of catalase is not altered after immobilization, although substrate diffusion through the original thin layer of membranes may become rate controlling. © 1993 John Wiley & Sons, Inc.
    Additional Material: 3 Ill.
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  • 2
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 196 (1992), S. 169-177 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Katalase wurde durch photoinduzeirte Propfpolymerisation auf mikroporöse polymere Trägermembranen immobilisiert. Die katalytische Aktivität für Zersetzung von Wasserstoffperoxid unter Ultrafitrationsbedingungen wurde mittels eines Rezirkulationsapparates untersucht. Die Membranen zeigten ein sehr gutes katalytisches Verhalten; die Enzymreaktion fand ausschließlich in der Membranstruktur statt. Anfangsreaktionsgeschwindigkeiten, gemessen in einem Temperaturbereich von 5-35°C als Funkation der Substratkonzentration und der Menge des immobilisierten Enzyms pro Einheit Membranoberfäche zeigten, daß sich der Reaktionsmechanismus der Katalase durch die Immobilisierung nicht verädert.
    Notes: Catalase has been immobilized in membranes prepared by photoinduced grafting onto microporous polymeric supports and its catalytic activity on hydrogen peroxide decomposition has been studied under ultrafiltration conditions by means of a recirculation apparatus. The membranes showed a very good catalytic performance and the enzyme reaction took place exclusively within the membrane structure. Initial reaction rates measured in the temperature range 5 - 35°C as a function of both substrate concentration and enzyme amount immobilized per unit membrane surface indicate that the mechanism of action of catalase is not altered after immobilization.
    Additional Material: 2 Ill.
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  • 4
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die photochemisch induzierte Pfropfcopolymerisation von 4-(N-Ethyl-N-2-acryloxiethyl)amino-4′-nitro-azobenzol I auf Cellulose wurde nach Eindampfen der Monomerlösungen in fester Phase bei 30°C untersucht. Aus dem zeitlichen Verlauf der Pfropfreaktion lassen sich zwei Geschwindigkeitskonstanten erkennen. Ein kinetisches Schema wird vorgeschlagen: im Frühstadium wird die adsorbierte Schicht von I unter photoinitiierter H-Abspaltung aus der Celluloseoberfläche nach einem selbstsensibilisierten Reaktionsmechanismus gepfropft; im zweiten Stadium werden die angrenzenden festen Schichten des Farbmonomeren I nach einem photochemisch induzierten Polymerisationsmechanismus aufgepfropft. Der gleichzeitig auftretende partielle Photoabbau des Farbstoffes wird anhand der ihm zugrunde liegenden Mechanismen diskutiert.
    Notes: Photochemically induced grafting and graft-polymerization of 4-(N-ethyl-N-2-acryloxyethyl)amino-4′-nitro-azobenzene I, brought into contact in the solid state with cellulose by evaporation of solvent from monomer solutions, has been investigated kinetically at 30°C. Two constant rate periods were observed. The first one was interpreted on the basis of a self-sensitized grafting mechanism of monomeric or oligomeric species of I, photochemically initiated by hydrogen abstraction from the cellulose surface. The second one was explained as a self-sensitized photochemically induced graft-polymerization of I on the first grafted layer. Some particular features, such as concurrent photodegradation of the first grafted layer at low surface coverage, are discussed in the light of the proposed mechanism.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 32 (1986), S. 4323-4331 
    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: Photoinitiated grafting and graft polymerization of liquid mixtures, adsorbed onto polypropylene, polycaprolactam, and poly(ethylene terephthalate) films, containing one of four acryloxy-substituted aromatic diazenes and one of four diacrylate comonomers, in the presence of 1,2-diphenyl-2,2-dimethoxyethanone as photoinitiator, were investigated kinetically at 30 ± 2°C. Irradiation was carried out polychromatically, with impinging photoenergy from 2.1 × 10-8 to 20.5 × 10-8 einstein s-1 cm-2; in some of the runs the ultraviolet radiation was filtered. The ratio R between the molar concentration of photoinitiator and the sum of concentrations of dye and diacrylate varied between 0.005 and 0.095; the ratio M between the molar concentration of dye and diacrylate varied between 0.005 and 0.046. The moles of dye and diacrylate n initially deposited per unit apparent polymeric surface S varied between 2 and 74 μmol cm-2.No selective effect was shown by the presence of dyes in the comonomer mixture. The surface density of grafted molecules at the end of the grafting process was not affected by the photoinitiator concentration (for 0.030 〈 R 〈 0.095), by diacrylate or dye concentrations, or by the kind of polymer substrate. This parameter, on the contrary, clearly depended on n/S, and linearly up to n/S ≅ 30 μmol cm-2. Quantum efficiencies for the two consecutive kinetic processes of grafting and graft polymerization (Φ1 and Φ2, respectively) were evaluated. The dependency of Φ1 on R, as well as of Φ2 on n/S, are critically discussed on the basis of the proposed mechanism involving grafting of an oligomeric chain (Φ1 values up to the order of 102) followed by a step-by-step graft polymerization (Φ2 limiting values of the order of unity). The sensitizing effect of acryloxy-substituted aromatic diazenes on both Φ1 and Φ2 is evidenced.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 3185-3195 
    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: A model has been applied to release of plasticizers from polymer films through vapor phase, for which the overall rate of release may be generally determined by evaporation of the plasticizer from the surface of the film, and/or by migration to the surface at below saturation in the polymer. The experimental system employed made use of n-butyl formate, diethyl-phthalate, di-n-butylphthalate, and N,n-butylbenzenesulfonamide as model molecules in polycaprolactam films, both with the aims of studying undesirable loss of plasticizers, and of simulating a model able to envisage releasing, at a constant rate, of any desired additive, with relatively high solubility and vapor pressure, to the content of packaging films. Experimental measurements were made (at 298-333 K) by investigating in a suitable cell the permeation of plasticizers both at concentrations below and above the saturation limit. Rate of evaporation of plasticizers from the membrane surface above the saturation limit, measured in this cell, were found to coincide satisfactorily with those calculated by application of the mass transfer theory to evaporation from a stationary liquid into a stirred gas, at a known velocity of gas flowing past the surface. From these latter rates and solubilities, the mass transfer coefficients H for evaporation could be obtained, as well as from experimental time lags the diffusivities Dp through the polymer membrane. In the light of the theoretical model a correlation was found between activation energies of H and evaporation enthalpies of the model molecules.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 5 (1992), S. 55-61 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Long-lived trapped radicals produced during the photopolymerization of butane-1, 4-diol diacrylate (BDDA) were studied by EPR and ENDOR spectroscopy and their thermal decay was followed by EPR measurements at different temperatures (40-120 °C) for kinetic study. The EPR signal showed the superimposition of two different patterns, a three-line and a single-line spectrum. Both EPR patterns decayed following first-order kinetics in the investigated temperature range. Activation parameters of the decay were obtained. The EPR patterns were attributed to the same radical species situated in fluid and in cross-linked regions of the photopolymerized BDDA. Radicals of the latter kind undergo electron spin exchange strong enough to wash out the hyperfine splitting. The single-line width is mainly determined by electron spin dipole-dipole interactions. The ENDOR response is only of the matrix kind, typical of radicals in a solid phase. The present model was also compared with recent literature reports.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 197 (1996), S. 497-507 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The EPR spectra of radicals produced during the photoinduced polymerization and cross-linking of multifunctional acrylic and methacrylic monomers are sensitive to the mobility of the polymeric surroundings. An analysis of the rate of decay of radicals trapped in different environments is reported, with the aim of finding a correlation between the evolution of the EPR spectral shape and the characteristics of the polymeric structure. A dispersive kinetic model was found to be suitable for the interpretation of radical decay results, in terms of a rate parameter (B) and a dispersion parameter (α) which takes into account the disorder of the system. These parameters depend on radical decay temperature and reflect the properties and the mobility of the photopolymerized networks, in relation to the monomer structure and to photopolymerization conditions, such as irradiation time and photoinitiator content.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 195 (1994), S. 661-669 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal polymerization and cross-linking of 1,4-butanediol diacrylate taking place after irradiation was followed kinetically in the temperature range from 60 to 140°C. Low conversions were reached by polychromatic pre-irradiation in the absence of any photoinitiating species. The disappearance of double bonds follows first-order kinetics, up to degree of conversion 0,4 〈 x 〈 0,5, and then proceeds up to high x values, according to a multiple relaxation phenomenon, characterized by the same mean relaxation lifetime as first-order kinetics. Activation parameters also were calculated. The present results on the decay of double bonds are discussed in the framework of the classical polymerization mechanism and in connection with previous kinetical data on the decay of radicals trapped in the same pre-irradiated monomer, obtained by electron paramagnetic resonance (EPR) measurements. Propagation and termination processes depend in the same way on the mobility of the vitrified polymerized network, both being diffusion-controlled.
    Additional Material: 2 Ill.
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  • 10
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The electron paramagnetic resonance (EPR) spectra obtained from radicals produced during the photopolymerization of multifunctional acrylic and methacrylic monomers have been interpreted by taking into account the EPR line-broadening due to dynamic exchange between two conformations of the β-methylene groups and a spin-spin dipolar interaction between radicals trapped in rigid regions of the polymer. From 1H matrix electron and nuclear double resonance (ENDOR) spectra the distance between the radical center and the surrounding shells of protons can be estimated.
    Additional Material: 6 Ill.
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