Recent advances in poly

Recent Advances in Poly(meth)acrylate Based Blends and Composites... 

Recent advances in poly (urethane) reinforced reaction injection molded (RRIM) parts has led to use in components such as fenders for small trucks, low-density interior door panels, and higher heat-resistant body panels. Rear fenders on the Chevrolet Silverado and the GMC Sierra trucks (Fig. 2), made of RRIM polyurea, are the first application of a RRIM polymer designed to withstand electrocoat, primer, and topcoat paint line process temperatures. 

The study of acid-base interaction is an important branch of interfacial science. These interactions are widely exploited in several practical applications such as adhesion and adsorption processes. Most of the current studies in this area are based on calorimetric studies or wetting measurements or peel test measurements. While these studies have been instrumental in the understanding of these interfacial interactions, to a certain extent the interpretation of the results of these studies has been largely empirical. The recent advances in the theory and experiments of contact mechanics could be potentially employed to better understand and measure the molecular level acid-base interactions. One of the following two experimental procedures could be utilized (1) Polymers with different levels of acidic and basic chemical constitution can be coated on to elastomeric caps, as described in Section 4.2.1, and the adhesion between these layers can be measured using the JKR technique and Eqs. 11 or 30 as appropriate. For example, poly(p-amino styrene) and poly(p-hydroxy carbonyl styrene) can be coated on to PDMS-ox, and be used as acidic and basic surfaces, respectively, to study the acid-base interactions. (2) Another approach is to graft acidic or basic macromers onto a weakly crosslinked polyisoprene or polybutadiene elastomeric networks, and use these elastomeric networks in the JKR studies as described in Section 4.2.1. 

Recent advances in complexes of group VIB metals (Mo, W) with poly-(pyrazolyl)borate ligands 98MI2. 

Abstract Many similarities between the chemistry of carbon and phosphorus in low coordination numbers (i.e.,CN=l or 2) have been established. In particular, the parallel between the molecular chemistry of the P=C bond in phosphaalkenes and the C=C bond in olefins has attracted considerable attention. An emerging area in this field involves expanding the analogy between P=C and C=C bonds to polymer science. This review provides a background to this new area by describing the relevant synthetic methods for P=C bond formation and known phosphorus-carbon analogies in molecular chemistry. Recent advances in the addition polymerization of phosphaalkenes and the synthesis and properties of Tx-con-jugated poly(p-phenylenephosphaalkene)s will be described. 

Cornblath DR, Hoke A (2006) Recent advances in HIV neuropathy. Curr Opin Neurol 19(5) 446-450 Cornblath DR, McArthur JC (1988) Predominantly sensory neuropathy in patients with AIDS and AIDS-related complex. Neurology 38(5) 794-796 Cornblath DR, McArthur JC et al (1987) Inflammatory demyeUnating peripheral neuropathies associated with human T-cell lymphotropic virus type III infection. Ann Neurol 21(l) 32-40 Corral I, Quereda C et al (1997) Acute poly radiculopathies in HIV-infected patients. J Neurol 244(8) 499-504... 

Peruzzini, M. Poli, R. Recent Advances in Hydride Chemistry 2001, Elsevier Science Amsterdam. 

Recent advances in the development of well-defined homogeneous metallocene-type catalysts have facilitated mechanistic studies of the processes involved in initiation, propagation, and chain transfer reactions occurring in olefins coordi-native polyaddition. As a result, end-functional polyolefin chains have been made available [103].For instance, Waymouth et al.have reported about the formation of hydroxy-terminated poly(methylene-l,3-cyclopentane) (PMCP-OH) via selective chain transfer to the aluminum atoms of methylaluminoxane (MAO) in the cyclopolymerization of 1,5-hexadiene catalyzed by di(pentameth-ylcyclopentadienyl) zirconium dichloride (Scheme 37). Subsequent equimolar reaction of the hydroxyl extremity with AlEt3 afforded an aluminum alkoxide macroinitiator for the coordinative ROP of sCL and consecutively a novel po-ly(MCP-b-CL) block copolymer [104]. The diblock structure of the copolymer... 

Interpolymer complexation between water-soluble polymers by hydrogen bonding was a frontier subject in the 1970s. Polyfcarboxylic acids), mainly po-lyfacryhc acid) (PAA) and poly( methacryflc acid) (PMAA), served as the most common proton-donating components. As for the proton-accepting polymers, poly(ethylene oxide ) (PEO or PEG) and poly(M-vinyl-2-pyrrolidone) (PVPo) were often used. The important results on the formation of complex aggregates and its dependence on the structur prameters have been reviewed [2,3,8]. In this section we select a few representative topics to look at recent advances in interpolymer complexes in aqueous media, with the emphasis on fluorescence probe studies. 

Several of the originally planned chapters, on comparison of silicon compounds with their higher group 14 congeners, interplay between theory and experiment in organisilicon chemistry, silyl radicals, recent advances in the chemistry of silicon-phosphorous,-arsenic,-antimony and -bismuth compounds, and the chemistry of poly silanes, regrettably did not materialize. We hope to include these important chapters in a future complementary volume. The current pace of research in silicon chemistry will certainly soon require the publication of an additional updated volume. 

M. Peruzzini and R. Poli (eds.), Recent Advances in Hydride Chemistry, Elsevier, Amsterdam, 2001. 

In this section, we discuss a recent advance in the cell model of poly electrolytes. In the cell model, a cylindrically shaped polyion with all its counterions reside in a cell. The cell is assumed to be cylindrical. The total charge in each cell is zero. Within the framework of cell model, thermodynamic quantities including counterion and co-ion distributions have been studied and compared with the counterion condensation model [45, 46]. 

In this review dealing with recent advances in membrane science, the term membrane" will be used to indicate any medium which acts as a barrier to transport into or out of a region, provides selective transfer of one species over another or regelates the transport of a material to its environment at a controlled rate. In addition to the common usage of the word membrane" to indicate a dense polymer film, the above definition includes a variety of interesting cases such as highly porous ultrafiltration membranes and hydrophobic liquid membranes with selectivity properties which can be tailored by incorporation of materials which selectively complex with one of the species to be processed. The important topics of controlled release of chemicals from polymeric devices and removal of volatile monomers from addition polymers such as poly (vinyl chloride and poly (acrylonitrile are also treated here. 

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