Preparation and characterization of rubber‐toughened poly(trimethylene terephthalate)/organoclay nanocomposite

Rubber‐toughened poly(trimethylene terephthalate) (PTT)–organoclay nanocomposite (RTPTTCN) was prepared by a melt mixing technique. The rubber‐toughened PTT (RTPTT) was made by blending it with ethylene propylene diene terpolymer (EPDM) and with a small amount of maleated EPDM as a compatibilizer. XRD and TEM analysis indicated that the RTPTTCN forms a partially exfoliated nanocomposite. It was observed from SEM analysis that the clay nanoparticles induced a reduction of rubber particle size in the PTT matrix. Tensile and dynamic mechanical analysis indicated that the clay nanoparticles enhance the stiffness of the RTPTT without adversely affecting its toughness. Melt rheological studies revealed that the nanocomposites exhibited strong shear thinning behavior, and a percolated network of the clay particles was formed. It was also observed from DSC that the clay nanoparticles caused an increase in the nonisothermal crystallization temperature of the PTT. POLYM. ENG. SCI., 47:863–870, 2007. © 2007 Society of Plastics Engineers     

Thermal degradation of cellulose and its phosphorylated products in air and nitrogen

The thermal degradation of cellulose and its phosphorylated products (phosphates, diethylphosphate, and diphenylphosphate) were studied in air and nitrogen by differential thermal analysis and dynamic thermogravimetry from ambient temperature to 750°C. From the resulting data various thermodynamic parameters were obtained following the methods of Broido and Freeman and Carroll. The values of E_a for decomposition for phosphorylated cellulose were found to be in the range 55–138 kJ mol^?1 in air and 85–152 kJ mol^?1 in nitrogen and depended upon the percent of phosphorus contents in the samples. The mass spectrum of cellobiose phosphate indicated the absence of the molecular ion, indicating that the compound was thermally unstable. The IR spectra of the pyrolysis residues of cellulose phosphate gave indication of formation of a compound having C?O and P?O groups. A fire retardancy mechanism for the thermal degradation of cellulose phosphate has been proposed.     

Structure and dynamics of a pentablock copolymer of polystyrene-polybutadiene in a butadiene-selective solvent

We have examined solutions of a polystyrene-polybutadiene pentablock copolymer in n-heptane, a strongly selective solvent for polybutadiene. Small angle neutron scattering from 7 to 15% samples reveals domains about 10 nm in radius formed by the association of 200 polystyrene blocks. Dynamic light scattering measurements on 8 and 9% samples showed three modes: a fast diffusive mode related to the collective diffusion in semidilute solutions/gels; a relaxational mode related to the local dynamics of polystyrene domains trapped in the gel formed by bridging the domains with the polybutadiene chains; and a very slow diffusive mode. The relaxational dynamics persisted over the entire temperature range, becoming faster with increasing temperature, indicating a decreased microviscosity at higher temperatures. The slow dynamics seems to be connected with heterogeneities in the physical gel due to microsyneresis and almost disappeared above 50 °C. Macroscopic phase separation into two liquid phases was observed in a dilute solution of the un-associated copolymer, and into a liquid and gel phase at higher concentrations. The absence of flower-like micelles in dilute solutions and the macroscopic phase seperation suggest that the gels in the pentablock are formed by random association of multiplet domains and not by bridging of micellar domains.     

Grafting poly(t‐butyl acrylate) to poly(allylamine) by inverse microemulsion radical polymerization: From comb‐polymer to amphiphilic shell crosslinked polymer nanocapsule

An interfacial grafting radical polymerization method for amphiphilic comb copolymer and shell crosslinked polymer nanocapsules was reported. Macropolyradicals on a water soluble long chain polyamine were generated with hydrogen peroxide in the water phase and subsequent grafting radical polymerization of a vinylic monomer at the water/oil interface proceeded at 65°C. In the presence of a crosslinker, the resulting graft copolymer formed a defined core‐shell structure with hydrophilic aqueous core functionalized by the polyamine and a hydrophobic crosslinked polymer shell. The structure of the core‐shell material was characterized by NMR, FTIR, DSC, TGA, SEM, TEM, and the mechanism of the graft polymerization is proposed. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1905–1911, 2007     

IR studies on preoxidized PAN fibres

IR absorption spectra of preoxidized PAN fibres have been studied in the spectral region 2–15 μ. Observed frequencies have been assigned to the different modes of vibration. The neighbouring frequencies appearing in the stretching mode region of the nitrile group has been interpreted in terms of Fermi-resonance and a basis for the correlation between their intensity ratio and the degree of oxidation has also been discussed.     

Retardation effect of superplasticizer on different cement fractions

Cement hydration is a complex chemical process strongly influenced by the proportions of the various minerals present in the cement, admixtures, and the size of the cement particles. In this note, it is shows that naphthalene based superplasticizer, used at high dosage, does not affect the total heat of hydration but retards the hydration process of portland cement. This retardation, however, is most effective on the medium size fraction of the cement (4 – 30 μm in our case). The superplasticizer does not affect the hydration of the fine fraction (< 4 μm) to that extent due to its richer concentration of SO₃ and alkalies. The coarse fraction of the cement (30 – 72 μm) does not participate (with or without superplasticizer) in the heat evolution process.     

Hydration/dehydration characteristics of struvite and dittmarite pertaining to magnesium ammonium phosphate cement systems

Struvite, an important reaction product in magnesium ammonium phosphate cement systems, was synthesized in the laboratory. The elevated-temperature dehydration and then roomtemperature hydration characteristics of the dehydrated products were studied by thermogravimetric analyses and X-ray diffraction techniques. From isothermal experiments, struvite is found to be thermally unstable in air at temperatures above 50 C. Struvite can lose part or all of its ammonia and water molecules depending on the time and temperature of heat treatment, ultimately forming magnesium hydrogen phosphate. This decomposed product is X-ray amorphous and upon room-temperature rehydration can form struvite, unknown hydrates or newberyite, alone or in combination with each other, depending on the amount of ammonia left in the structure. However, when struvite is heated in excess water, it only loses its water of crystallization to form the monohydrate, dittmarite. Dittmarite is thermally more stable than struvite and like struvite also forms magnesium hydrogen phosphate on decomposition. At room temperature and in the presence of excess water, dittmarite can slowly transform to the hexahydrate, struvite. The consequence of structural similarities between struvite and dittmarite and conditions under which they may be present in cured cements are described.     

IndoorSense: context based indoor pollutant prediction using SARIMAX model

Multimedia Tools and Applications - Indoor air pollutants e.g., Carbon dioxide (CO2), Particulate Matter(PM)2.5, PM10, Total Volatile Organic Compounds (TVOC), etc. have a serious impact on human...     

Lab-scale feasibility study on new elastomer comprising chloroprene and acrylonitrile for oil and gas applications

The limited options of suitable elastomers with adequate cost-performance balance drive the necessity to introduce new materials in the oil & gas (O&G) application space. The relevance of a recently developed copolymer of chloroprene and acrylonitrile (referred to as acrylonitrile–chloroprene rubber or NCR) to O&G applications is described in this technical contribution. The new elastomer demonstrates adequate physical properties and reasonably good high and low-temperature capabilities. It offers good resistance to several aqueous and non-aqueous fluids with low volume swelling and retains its physical properties to reasonable extents while exposed to hot test oils. Acrylonitrile–chloroprene rubber has been found to sustain “sour gas” exposure. Good abrasion resistance, high tear strength, and remarkably high flex-fatigue resistance coupled with low heat build-up reflect its durability under dynamic conditions. In addition, acrylonitrile–chloroprene rubber can very well withstand the rapid gas decompression test at 25°C. This unique combination of attributes may allow acrylonitrile–chloroprene rubber to be considered as a candidate material for high-performance O&G applications.