Morphological,mechanical, and rheological studies of PVC/ABS blends in the presence of maleic anhydride

A novel method of enhancing compatibility in PVC/ABS blends is the use of ABS‐grafted‐(maleic anhydride) (ABS‐g‐MAH) as a compatibilizer. In this study, maleic anhydride was grafted onto ABS (initiated by peroxide) in an internal mixer. Grafting degree was determined by a back‐titration method, and certain amounts of the resultant ABS‐g‐MAH were added to PVC/ABS blends during their melt blending in the mixer. The weight ratio of PVC to ABS was kept at 70:30. Evaluation of compatibilization was accomplished via tensile and notched Izod impact tests, scanning electron microscopy (SEM), and rheological studies. According to the SEM micrographs, better dispersion of the rubber phase and its finer size in properly compatibilized blends were indications of better compatibility. Besides, in the presence of a proper amount [5 parts per hundred parts of PVC (php)] of ABS‐g‐MAH, PVC/ABS blends showed significantly higher impact strengths than uncompatibilized blends. This result, in turn, would be an indication of better compatibility. In the presence of 5 php of compatibilizer, the higher complex viscosity and storage modulus, as well as a lower loss modulus and loss factor in the range of frequency studied, indicated stronger interfacial adhesion as a result of interaction between maleic anhydride and the PVC‐SAN matrix. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers     

Unique structure of fibrous ZSM-5 catalyst expedited prolonged hydrogen atom restoration for selective production of propylene from methanol

A unique mesostructured fibrous silica@ZSM-5 (HSi@ZSM-5) catalyst was synthesized via microemulsion ZSM-5 zeolite seed assisted synthesis method and successfully applied in enhanced propylene formation in methanol to olefin (MTO) process. Characterization of the catalysts were carried out by FESEM, TEM, XRD, TGA, N₂ adsorption-desorption, NH₃ and KBr probed FTIR. Catalytic performance of as-synthesized catalyst was examined using a micro-pulse reactor and compared with the commercial HZSM-5. The reaction mechanism was elucidated by in-situ methanol FTIR spectroscopy. It was found that HSi@ZSM-5 produced higher propylene selectivity (56%) and was stable for long time on stream (80 h), nearly three-fold higher than that of commercial HZSM-5. In addition, HSi@ZSM-5 displayed higher rate of methanol dehydration, surface methoxy species generation and olefin methylation, indicating that alkene catalytic cycle is the dominant reaction mechanism. The higher selectivity towards propylene was correlated to the existence of moderate acidity which impeded the formation of paraffins and polymethylbenzene intermediates. These observations are further supported by KBr probed FTIR findings which revealed negligible paraffinic carbon species on HSi@ZSM-5. Thus, the unique fibrous silica@ZSM-5 retarded coke deposition due to suppression of undesired side reactions thereby signifying intensified propylene formation, which is highly desirable in commercial MTO processes.     

Enhanced hydrogen-assisted cracking of 1,3,5-triisopropylbenzene over fibrous silica ZSM-5: Influence of co-surfactant during synthesis

In this study, unique fibrous silica ZSM-5 was successfully synthesized by using three type of alcohol possessing different alkyl-chain length as the co-surfactant. The effect of diverse co-surfactant was observed in the changes of physical properties, such as crystallinity, inter-dendrimer distances and pore properties. According to the IR and temperature programmed desorption of ammonia (NH₃-TPD) analyses, all catalysts exhibited different acid strengths which could be triggered by the different amount of additional silica species. All catalysts exhibited high catalytic performance in the hydrocracking of 1,3,5-triisopropylbenzene due to the absence of diffusion limitation. However, FZSM5C3 exhibited the highest catalytic activity which corresponded to its high number of Brønsted acid sites. It was observed that different length of co-surfactant alkyl-chain has resulted in different degree of oil penetration into the microemulsion system which subsequently triggered in various inter-dendrimer distances and amount of incorporated silica species. Hence, the altered physicochemical properties led to the difference in catalytic performance due to the presence of different number of Brønsted acid sites.     

Supplementing with L-Tryptophan Increases Medium Protein and Alters Expression of Genes and Proteins Involved in Milk Protein Synthesis and Energy Metabolism in Bovine Mammary Cells

The objective of this study was to investigate the effects of supplementing with L-tryptophan (L-Trp) on milk protein synthesis using an immortalized bovine mammary epithelial (MAC-T) cell line. Cells were treated with 0, 0.3, 0.6, 0.9, 1.2, and 1.5 mM of supplemental L-Trp, and the most efficient time for protein synthesis was determined by measuring cell, medium, and total protein at 0, 24, 48, 72, and 96 h. Time and dose tests showed that the 48 h incubation time and a 0.9 mM dose of L-Trp were the optimal values. The mechanism of milk protein synthesis was elucidated through proteomic analysis to identify the metabolic pathway involved. When L-Trp was supplemented, extracellular protein (medium protein) reached its peak at 48 h, whereas intracellular cell protein reached its peak at 96 h with all L-Trp doses. β-casein mRNA gene expression and genes related to milk protein synthesis, such as mammalian target of rapamycin (mTOR) and ribosomal protein 6 (RPS6) genes, were also stimulated (p < 0.05). Overall, there were 51 upregulated and 59 downregulated proteins, many of which are involved in protein synthesis. The results of protein pathway analysis showed that L-Trp stimulated glycolysis, the pentose phosphate pathway, and ATP synthesis, which are pathways involved in energy metabolism. Together, these results demonstrate that L-Trp supplementation, particularly at 0.9 mM, is an effective stimulus in β-casein synthesis by stimulating genes, proteins, and pathways related to protein and energy metabolism.     

Enhancement in Physical Properties of Silver-Doped Fe–Ni Invar Nano-alloy Using Chemical Reduction Method

Journal of Superconductivity and Novel Magnetism - Silver-substituted Fe–Ni nano invar alloy is a new and innovative field of research due to their interesting invar, magnetic and electrical...     

A Study of the Effect of Aluminium on the Mechanochemical Reduction of Hematite by Graphite

The effect of addition of small amounts of aluminium on mechano‐chemical reduction of hematite by graphite was studied. Various amounts of aluminium (0 to 10%) were added to a hematite‐graphite mixture, in which C/O ratio was 1:1. The hematite‐graphite‐aluminium mixtures were then subjected to ball milling followed by heating up reduction. The heating up reduction was carried out in Ar atmosphere, using TG‐DTA device. In TG‐DTA experiments, samples were heated by a constant heating rate of 10 °C/min from room temperature up to 1100 °C and maintained for 30 minutes at this temperature. To clarify the reactions which took place during milling and heating up reduction, the samples were subjected to XRD examinations. It was found that the heat generated during exothermic reaction of aluminothermic reduction of hematite promoted the endothermic reaction of carbothermic reduction. In the course of heating up reduction, the carbothermic reaction occurred just after aluminothermic reaction. Increasing of aluminum content from 0 to 10% in 2 hours ball milled samples decreased the temperature of carbothermic reaction from 1020 °C to about 860 °C. The further ball milling of the samples up to 5 and 10 hours, for the samples containing 10 and 5% aluminium respectively, caused the decrease of the temperature of aluminothermic and carbothermic reactions to around the melting point of aluminium.     

The effect of initiator‐to‐monomer ratio on the properties of the polybutadiene‐ol synthesized by free radical solution polymerization of 1,3‐butadiene

Polybutadiene‐ol was synthesized by solution radical polymerization of 1,3‐butadiene in the presence of hydrogen peroxide as initiator and 2‐propanol as solvent. The ratio of initiator to monomer molar concentration, [I₀]/[M₀], was varied while temperature, reaction time and the type and amount of solvent were kept constant. The effects on the M_n; M_w; M_v; PDI, OH‐number and functionality of the synthesized polyols were studied. By taking several samples during a polymerization batch and analyzing them, the time of reaction was chosen as 100 min, after which the PDI changed dramatically. M_n decreased exponentially with increasing [I₀]/[M₀] according to the relationship M_n = 565.55 ([I₀]/[M₀])^?0.7553. The decrease observed in M_w gradually levelled off with increasing [I₀]/[M₀] and molecular weight distribution broadened at larger values of [I₀]/[M₀]. The OH‐number increases with [I₀]/[M₀]. In addition to the number‐average molecular weight, functionality is dependent on the number of hydroxyl‐terminated chain radicals in the reaction medium. Copyright © 2003 Society of Chemical Industry     

Synthesis and Antifungal Activity of Some Organotin(IV) Carboxylates

Six diorganotin(IV) carboxylates prepared by reacting diorganotin(IV) dichlorides with the respective silver carboxylate have been tested for antifungal activity against Aspergillus. niger, Aspergilluus flavus and Pencillium. citrinum in Sabourand dextrose broth. The compounds generally exhibit greater fungitoxicity than the diorganotin(IV) dichlorides and the carboxylic acids from which they were synthesized. In keeping with the generally accepted notion that the organotin moiety plays an important role in deciding the antifungal activity of an organotin compound, the diphenyltin(IV) compounds were more active than their di-n-butyltin(IV) analogues. However, the order of increasing fungitoxicity of the compounds parallels that of the uncomplexed carboxylic acids. The implications of the results are discussed.     

Competency‐based IT personnel selection using a hybrid SWARA and ARAS‐G methodology

In the knowledge economy, human capital is a key factor in any organization to achieve a sustainable competitive advantage. Thus, selection of competent personnel is the most important function of human resource managers. However, because of a wide range of criteria and organizational factors that affect the process, personnel selection is often regarded as a complex problem that can be answered through multicriteria decision‐making (MCDM) procedures. Despite the great importance of determining a comprehensive set of criteria, it has not gained enough attention in the literature. This study presents a competency framework with five criteria for choosing the best information technology (IT) expert from five alternatives. The stepwise weight assessment ratio analysis (SWARA) and grey additive ratio assessment (ARAS‐G) methods are also used to derive the criteria weights and provide the final alternative, respectively. The results reveal that subject competency is the major criteria in IT personnel selection.