Comparative study of the release kinetics of osmotically active solutes from hydrophobic elastomeric matrices combined with the characterization of the depleted matrices

The release process of three osmotically active solutes with various solubilities in water (NaCl, CsNO₃, and CsCl) from silicone rubber matrices is presented. The kinetics of release for different initial loads of the salts were supplemented by measurements of the kinetics of concurrent water uptake. To gain insight on the relevant non‐Fickian transport mechanisms, the morphology, the diffusion and sorption properties and the physicochemical state of water in the salt‐depleted matrices were studied. In addition, both salt‐loaded and salt‐depleted matrices were characterized with respect to their mechanical properties. The combined information, derived from these techniques, supported the operation of a release mechanism carried out through the formation of microscopic cracks, interconnecting the permanently formed cavities inside the matrices. The results indicate that these microscopic cracks may have healed upon drying. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Preparation and investigation of ethylene–vinyl acetate copolymer/silicone rubber/clay nanocomposites

In this article, the combination of silicone rubber (SR) elastomer with synthetic iron montmorillonite (Fe‐MMT) to form a kind of new flame‐retardant system based on an ethylene–vinyl acetate (EVA) copolymer is first reported. Also, the flame retardancy of the EVA/SR/Fe‐MMT hybrid are compared with that of EVA/SR/natural sodium montmorillonite. The structures of the nanocomposites were characterized with X‐ray diffraction and transmission electron microscopy. Cone calorimeter tests and thermogravimetric analysis were used to evaluate the flame‐retardant properties and thermal stability of the composites, respectively. In addition, tensile tests were carried out with a universal testing machine, and the morphology of the fracture surface was observed with environmental scanning electron microscopy. We found that SR/organophilic montmorillonite (Fe‐OMT) was more effective in reducing the primary peak heat release rate of the nanocomposite, and the EVA/SR/Fe‐OMT hybrid had a higher thermal stability in the deacetylated polymer than EVA/SR/sodium organophilic montmorillonite. Moreover, the exfoliated EVA/SR/Fe‐OMT nanocomposite displayed excellent mechanical properties because of a better dispersion of Fe‐OMT in the polymer matrix, and a possible mechanism is discussed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Polysiloxane‐lignin composites

A series of composites based on polydimethylsiloxane‐α,ω‐diol (PDMS) as polymeric matrix, silica aerogel as reinforcing filler, and the lignin powder—a biomass derivative, as bulking filler, have been prepared. Different weight ratios between components were used. The composites were investigated by scanning electron microscopy, dynamic mechanical analysis, tensile strength tests, X‐ray diffraction analysis, thermogravimetric analysis, and differential scanning calorimetry. The results were compared with those obtained on a reference sample prepared by using a classical material—diatomite and a pure crosslinked PDMS. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Melt spinning and metal chloride vapor curing process on polymethylsilsesquioxane as Si?O?C fiber precursor

Melt spinning process of polymethylsilsesquioxane (PMSQ) at 403–453 K was investigated as a Si? O? C fiber precursor in terms of averages and distributions of spun fiber diameters. Because of fusible character of PMSQ at low temperature, the spun fibers were exposed to vapors of various metal chlorides (SiCl₄, Si(CH₃)Cl₃, TiCl₄, and BCl₃) to promote the fiber curing. Cured fibers were investigated by FTIR and TG analyses. In a case of the fiber synthesized with SiCl₄ curing, tensile tests on the pyrolyzed fibers were performed. Exposure of the synthesized fiber at high temperature with a flame of an oxygen‐gas burner was examined. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Remarkable Efficiency Improvement in the Preparation of Insoluble Polymer‐Bound (IPB) Enantioselective Catalytic Systems by the Use of Silicone Chemistry

The use of platinum‐catalyzed hydrosilylation chemistry of silicones greatly simplifies the preparation of bis‐oxazoline (box) ligands covalently bound to an insoluble polymeric support. The use of such immobilized chiral ligands in different copper‐catalyzed asymmetric transformations (carbonyl‐ene, Mukaiyama aldol and olefin cyclopropanation reactions) allows the attainment of high levels of enantioselectivity (91–99 % ee).     

Fibrillation tendency of cellulosic fibers,part 6: Effects of treatments with additive polymers

The influences of the treatments with various polymers on fibrillation and abrasion resistances of lyocell materials were investigated with respect to the type of polymer, the polymer concentration, and the drying temperature. Fibril number, generated with agitation using ball‐bearings (FN_ball), was decreased with increasing the concentration of aminofunctional polysiloxane because of reduction in water retention capacity (WRV) in fibers. The never‐dried lyocell fiber showed smaller decrease in FN_ball because of its higher WRV when compared to dried fibers. The treatment with aminofunctional polysiloxane enhanced not only the fibrillation resistance but also abrasion resistance, which was indicated as rotation number of abrasive bar in the abrasion test (RN_abr). No fibrillation was obtained in the fiber treated with 10 g/L aminofunctional polysiloxane at 120°C for 20 min, while the fibers treated at 60 and 170°C for 15 min were fibrillated in the agitation and abrasion tests. The addition of secondary polyethylene derivative also reduced the fibrillation tendency of lyocell; however, the extent of the reduction was lesser when compared with aminofunctional polysiloxane. The treatments with polyacrylate, polyurethane, and polyisocyanate derivatives improved the fibrillation resistance in lyocell fabrics, while fiber abrasion resistance was not significantly improved by the treatment with those additives, except in polyisocyanate. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 4140–4147, 2006     

Redox initiation system of ceric salt and α,ω‐dihydroxy poly(dimethylsiloxane)s for vinyl polymerization

The redox system of ceric salt and α,ω‐dihydroxy poly(dimethylsiloxane) is used to polymerize vinyl monomers such as acrylonitrile and styrene to produce block copolymers. The concentration and type of α,ω‐dihydroxy poly(dimethylsiloxane) affects the yield and the molecular weight of the copolymers. The copolymers have about 20°C lower glass‐transition temperatures and much higher contact angle values than of the corresponding homopolymer of vinyl monomers, although the weight percent of α,ω‐dihydroxy poly(dimethylsiloxane) of the copolymers is in the range of 1–2%. © 2006 Wiley Periodicals Inc. J Appl Polym Sci 102: 2112–2116, 2006     

Water‐repellent finishing of cotton fabrics by ultraviolet curing

Cotton fabrics were water‐repellent‐finished by radical ultraviolet curing of silicone and urethane acrylates with different formulations. The fabrics were impregnated with undiluted resins and with toluene solutions or water emulsions. Moreover, cationic ultraviolet‐curable systems were also investigated, such as an epoxy‐functional polysiloxane and mixtures of an epoxy resin with hydroxyl‐containing silicone additives. The gel content and polymerization yield were considered for the ultraviolet‐curing process evaluation. Water‐resistance properties were determined in terms of the contact angle, wettability, moisture adsorption, and water vapor permeability measurements, whereas the morphology and surface composition of treated fabrics were examined with scanning electron microscopy and energy‐dispersive X‐ray analysis. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

A two‐step method for the synthesis of a hydrophilic PDMS interpenetrating polymer network

A hydrophilic PDMS (polydimethylsiloxane) surface was formed by the synthesis of an interpenetrating polymer network (IPN) in a two‐step process. In the first step, PDMS was loaded with crosslinker and initiator using a solvent that swells the PDMS. In the second step, the PDMS sample was submerged into a solution containing the hydrophilic monomer followed by a UV‐polymerization step. The choice of solvent in the second step is critical to obtain a hydrophilic surface. It can be concluded that the solubility parameter of the solvent should be above a threshold value. Hence, in the second step only sufficiently polar solvents will result in hydrophilic PDMS‐IPNs. These principles are illustrated by using N‐vinyl‐2‐pyrrolidone as the hydrophilic monomer forming PVP/PDMS‐IPNs. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008.     

改性有机硅柔软剂的合成

综述了各种改性有机硅柔软剂在纺织品整理方面的应用，介绍了它们的合成方法归纳了常用改性有机硅柔软剂的合成机理，指出了各种复配的重要作用．