Novel Short-chain Crosslinked Cationomeric Polyurethanes

Summary Novel PUs containing pyridinium moieties were synthesized by chain extending isocyanate endcapped prepolymers with N, N’-bis (2-hydroxyethyl) isonicotinamide. The pyridinium moieties in the PUs were chemically crosslinked using short-chain divalent quaternising agents. The polyurethane cationomers were characterized by spectral, thermal and mechanical analysis. Spectral results confirmed the quaternisation of tertiary nitrogen leading to crosslinking. Compared to conventional PUs, the crosslinked PU networks exhibited improved thermal stability. The damping value (i.e.) tan δ for cationomers were improved over a broad temperature range when compared to conventional PU.     

Thermal degradation of poly(dimethylsilylene) and poly(tetramethyldisilylene‐co‐styrene)

Thermal degradation of poly(dimethylsilylene) homopolymer (PDMS) and poly(tetramethyldisilylene‐co‐styrene) copolymer (PTMDSS) was investigated by pyrolysis‐gas chromatography and thermogravimetry (TG). PDMS decomposes by depolymerization, producing linear and cyclic oligomeric products, whereas PTMDSS decomposes by random degradation along the chain resulting in each monomeric product and various other combination products. The homopolymer was found to be much less stable than the copolymer. The decomposition mechanisms leading to the formation of various products are shown. The kinetic parameters of thermal degradation were evaluated by different integral methods using TG data. The activation energies of decomposition (E) for the homopolymer and the copolymer are found to be 122 and 181 kJ/mol, respectively, and the corresponding values of order of reaction are 1 and 1.5. The observed difference in the thermal stability and the values of the kinetic parameters for decomposition of these polymers are explained in relation with the mechanism of decomposition. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006     

Creep deformation of induction pressure welded 2·25Cr-1Mo steel

In this paper, experimental results involving the effect of stress and temperature on creep behaviour of induction pressure welded (IPW) 2·25Cr-1Mo steel are presented. Creep rupture tests were conducted at 550–700°C in steps of 50°C over a stress range of 112·5–180 MPa. Above 650°C failure of the specimen was enhanced due to the microstructural instability. Failure in the specimens occurred invariably in the heat affected zones (HAZ), and the fracture surfaces indicated ductile failure.     

Role of heat transfer and thermal conductivity in the crystallization behavior of polypropylene‐containing additives: A phenomenological model

The thermal conductivity of a filler and the thermal conductivity of a composite made from that filler influence the heat‐transfer process during melt processing. The heat‐transfer process from the melt to the mold wall becomes an important factor in developing the skin–core morphology. These aspects were examined in this study. The thermal conductivity of polypropylene–filler composites was estimated with a standard model for various fillers such as calcium carbonate, talc, silica, wollastonite, mica, and carbon fibers. The rate of cooling under given conditions, including the melting temperature, mold wall temperature, mass of the composite, and filler content, was estimated with standard heat‐transfer equations. The time to attain the crystallization temperature for polypropylene was evaluated with a regression method with differential temperature steps. The crystallization curves were experimentally determined for the different fillers, and from them, the induction period for the onset of crystallization was estimated. These observations were correlated with the expected trends from the aforementioned formalism. The excellent fit of the curves showed that in all these cases, the thermal conductivity of the filler and composite played a dominant role in controlling the onset of the crystallization process. However, the nucleation effects became important in the later stages after the crystallization temperature was attained. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2994–2999, 2003     

Saponification kinetic study of mica-acrylonitrile graft copolymers

Kinetics of alkaline hydrolysis of mica-acrylonitrile graft copolymers was studied. The dependence of alkali concentration and the time of hydrolysis on the degree of saponification was determined. Chemical and spectroscopical techniques were used to determine the mechanism of hydrolysis.     

Modeling and Simulation of Heat Transfer in Loaded Continuous Heat Treatment Furnace

HEAT UP processing is the basic step for the workloadin heat treatment for further processing.It is also anenergy-intensive process.Thus,correct prediction ofthe temperature variation and distribution in theworkload is of significance to ensure the final qualityof the parts and to reduce energy consumption and timeas well.There are some studies about the optimizationof heat treating process in continuous furnace.FurnXpert'11is developed to optimize furnace designand operation for many types…     

Propagation of correlations in local random quantum circuits

We derive a dynamical bound on the propagation of correlations in local random quantum circuits—lattice spin systems where piecewise quantum operations—in space and time—occur with classical probabilities. Correlations are quantified by the Frobenius norm of the commutator of two positive operators acting on disjoint regions of a one-dimensional circular chain of length L. For a time \(t=O(L)\), correlations spread ballistically to spatial distances \(\mathcal {D}=t\), growing at best, diffusively with time for any distance within that radius with extensively suppressed distance- dependent corrections. For \(t=\varOmega (L^2)\), all parts of the system get almost equally correlated with exponentially suppressed distance- dependent corrections and approach the maximum amount of correlations that may be established asymptotically.     

Mesoporous titanium dioxide nanocatalyst: a recyclable approach for one‐pot synthesis of 5‐hydroxymethylfurfural

The present study deals with the production of 5‐hydroxymethyl furfural (HMF) from fructose by chemo‐conversion method using chemical catalyst, conventionally achieved by microwave‐assisted dehydration process. Five different chemical catalysts, namely oxalic acid, phosphotungstic acid and mesoporous titanium dioxide nanoparticles (TNPs) were compared at constant conditions of which TNPs yielded a maxima of 33.95%. The optimum temperature and catalyst loading were found to be 200°C and 20%, respectively, at a 5% optimum substrate concentration during 15 min optimum reaction time to yield 61.53% HMF. The efficiency of synthesised TNPs was investigated further through reusability studies. TNPs were properly recycled and the catalytic activity recovery was good even after a 14 batch reactions. The specific surface area of the TNP obtained is about 105.46 m² /g and its pore‐volume is about 0.42 cm³ /g according to single point adsorption. A large accessible surface area combined with a minimal pore size (15.92 nm) obtained with mesoporous TNPs is desirable for better catalyst loading, high‐yield HMF, retention and reduced diffusion constraints.Inspec keywords: mesoporous materials, recycling, production management, dissociation, nanoparticles, nanotechnologyOther keywords: mesoporous titanium dioxide nanocatalyst, recyclable approach, one‐pot synthesis, 5‐hydroxymethyl furfural production, HMF, chemo‐conversion method, chemical catalyst, microwave‐assisted dehydration process, oxalic acid, phosphotungstic acid, mesoporous titanium dioxide nanoparticles, TNP