Investigation of surface-modified anhydrous borax utilisation in raw glazes

This study aims to determine the feasibility of preparing ceramic glaze using a surface-modified borate, which contributes boron to the composition without the need of a fritting process. In this context, surface modification of anhydrous borax powders (ABP) with magnesium stearate (MgSt) via dry powder coating is investigated. The surface modification of ABP with MgSt is optimised by employing modifier dosage of 0.5, 1, and 2?wt% and coating periods of 30, 60, and 120?min. The resulting powders are comparatively characterised via wettability, solubility, and dispersibility tests. The structural changes in surface-treated ABP are investigated using X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FT-IR) analyses. The results indicate that ABP surface could be switched from hydrophilic (17°) to hydrophobic (115°), its water solubility decreased from 40% to 10%, and a coating yield of approximately 74% was achieved with MgSt dosage of 1?wt% at a processing period of 2?h. Furthermore, FT-IR and XPS results indicated that MgSt is mainly coated over the surface of ABP via physical adsorption rather than chemical bonding. The glaze containing surface-treated ABP that was fired at 1050?°C, demonstrated complete melting and surface coverage without defects. Thus, effective dry coating as a single-step approach could be applied to obtain surface-modified ABP, which offers controlled solubility in glaze suspensions with improved dispersibility and excellent glaze coverage of the surfaces.     

Effects of flow induced orientation of ferromagnetic particles on relative magnetic permeability of injection molded composites

Composite samples consisting of ferromagnetic asymmetric particles incorporated into a polyolefin binder were injection molded using custom designed molds which produced preferential fiber orientations. The relative magnetic permeability values of the composites were measured as a function of the filler volume fraction, injection rate, gate diameter, temperature, aspect ratio of the fibers, and fiber orientation. Fiber orientation was affected by the molding conditions and controlled the relative magnetic permeability of the composites. The degree of fiber orientation was significantly affected by the size of the opening (gate) to the mold, or by the mold geometry going from an edge-gated cylindrical to a center-gated disk cavity. Relative permeability values of the composites were observed to increase when the fiber orientation and the applied field were parallel to one another. For instance, highly aligned composite samples exhibited up to 30% greater relative permeability values compared to those samples which exhibit fiber orientation distributions approaching a random distribution. To our knowledge this is the first study that provides data linking the fiber orientation distribution functions of ferromagnetic asymmetric particles to the relative magnetic permeability values of injection molded composites.     

Synthesis and polymerizations of novel bisphosphonate‐containing methacrylates derived from alkyl α‐hydroxymethacrylates

The synthesis and polymerizations of four novel bisphosphonate‐containing monomers are reported. The monomers were synthesized from reaction of ethyl and tert‐butyl α‐bromomethacrylates with 3,3‐bis(diethoxyphosphoryl)propanoic acid or with tetraethyl 4‐hydroxybutane‐1,1‐diyldiphosphonate. Their thermal bulk polymerizations, photopolymerizations and copolymerizations with poly(ethylene glycol) methyl ether methacrylate were investigated. The homopolymerizations resulted in polymers with values of 25 000–83 000 g mol^?1; the copolymerizations yielded soluble polymers with 22–34% incorporation of the new monomers; the photopolymerizations gave some structure–reactivity correlation; and one of the homopolymers, upon hydrolysis of its bisphosphonate groups, could interact with hydroxyapatite. © 2013 Society of Chemical Industry     

Dissolution study of BAMO/AMMO thermoplastic elastomer for the recycling and recovery of energetic materials

Abstract

This study involves the characterization and dissolution of a thermoplastic elastomer copolymer used as binder in the new generation of energetic materials. The thermoplastic binder is an oxetane based elastomer manufactured by Thiokol Corporation. Since the binder encapsulates other components in an energetic material formulation, its controlled dissolution is crucial to the recovery and recycle of all the energetic material ingredients. The polymeric binder was found to be highly soluble in ethyl acetate and THF. The dissolution rate data obtained under well defined flow dynamics was satisfactorily correlated with the film model. External mass transfer resistance was found to be generally important but became negligible for Reynolds numbers above 6.0×10⁴. The mass transfer coefficients calculated on the basis of the film model were found to be an Arrhenius function of temperature. The activation energy for the dissolution rates was estimated to be 4.8 kcal/mol.     

Effect of free water removal from early-age hydrated cement pastes on thermal analysis

In order to follow the progress of cement hydration by analytical techniques, the ongoing hydration reactions must be stopped by complete removal of free water. A comparison between solvent exchange, oven drying and vacuum drying, using thermal analysis, is presented for early-age hydrated cement pastes. Results show that oven drying at 105 °C accelerates hydration, causes dehydration of some hydrated cement phases and favours carbonation. Solvent exchange with ethanol, ether and methanol results in a strong absorption and an incomplete removal of solvents. FT-IR and XRD gave evidence of the formation of carbonate-like phases due to an interaction upon heating, i.e. during thermal analysis, between the strongly absorbed solvents and the cement compounds or hydrates. Vacuum drying reveals reliable results as no interaction products can be formed and the Ca(OH)₂ content, determined by thermal analysis, gives a good approximation of the real amount of Ca(OH)₂.     

A complementary study on novel PdAuCo catalysts: Synthesis,characterization, direct formic acid fuel cell application,and exergy analysis

At present, Pd containing (10–40 wt%) multiwall carbon nanotube (MWCNT) supported Pd monometallic, Pd:Au bimetallic, and PdAuCo trimetallic catalysts are prepared via NaBH₄ reduction method to examine their formic acid electrooxidation activities and direct formic acid fuel cell performances (DFAFCs) when used as anode catalysts. These catalysts are characterized by advanced analytical techniques as N₂ adsorption and desorption, XRD, SAXS, SEM-EDX, and TEM. Electronic state of Pd changes by the addition of Au and Co. Moreover, formic acid electrooxidation activities of these catalysts measured by CV indicates that particle size changes in wide range play a major role in the formic acid electrochemical oxidation activity, ascribed the strong structure sensitivity of formic acid electrooxidation reaction. PdAuCo (80:10:10)/MWCNT catalyst displays the most significant current density increase. On the other hand, lower CO stripping peak potential obtained for PdAuCo (80:10:10)/MWCNT catalyst, attributed to the awakening of the Pd-adsorbate bond strength down to its optimum value, which favors higher electrochemical activity. DFAFCs performance tests and exergy analysis reveal that fuel cell performances increase with the addition of Au and Co which can be attributed to synergetic effect. Furthermore, temperature strongly influences the performance of formic acid fuel cell.     

Electrosynthesis of hierarchical Cu2O–Cu(OH)2 nanodendrites supported on carbon nanofibers/poly(para-phenylenediamine) nanocomposite as high-efficiency catalysts for methanol electrooxidation

The development of highly efficient catalysts using inexpensive and earth-abundant metals is a crucial factor in a large-scale commercialization of direct methanol fuel cells (DMFCs). In this study, we explored a new catalyst based on copper nanodendrites (CuNDs) supported on carbon nanofibers/poly (para-phenylenediamine) (CNF/PpPD) nanocomposite for methanol oxidation reaction (MOR). The catalyst support was prepared on a carbon paste electrode by electropolymerization of para-phenylenediamine monomer on a drop-cast carbon nanofibers network. Afterwards, CuNDs were electrodeposited on the nanocomposite through a potentiostatic method. The morphology and the structure of the prepared nanomaterials were characterized by transmission electron microscope, scanning electron microscope, energy dispersive X-ray, X-ray diffraction, and X-ray photoelectron spectroscope. The results suggested that a three-dimensional nanodendritic structure consisting of Cu₂O and Cu(OH)₂ formed on the hybrid CNF/PpPD nanocomposite. The catalytic performance of CuNDs supported on CNF, PpPD and CNF/PpPD was evaluated for MOR under alkaline conditions. The CNF/PpPD/CuNDs exhibits a highest activity (50 mA cm^?2) and stability toward MOR over 6 h, with respect to CNF/CuNDs (40 mA cm^?2) and PpPD/CuNDs (36 mA cm^?2). This inexpensive catalyst with high catalytic activity and stability is a promising anode catalyst for alkaline DMFC applications.     

Computational analysis of fouling by low energy surfaces

Fouling is a cost increasing problem for a variety of industries including aerospace, chemical, petroleum, and food. There have been studies on mitigation of fouling some of which recommend use of lower surface free energy materials, manufactured by different techniques, as an alternative to conventional materials. Although modeling of fouling for a given surface has been an area of interest; there is a lack in the models about correlating the surface free energy with deposit amount computationally. In this study, computational model, including the effect of surface energy and operational parameters, was proposed and validated to estimate amount of foulants deposits and rate of deposition. Towards this purpose, four coated surfaces (Microlube/PTFE, TM117P, AMC148, and CNT) were compared with stainless steel (SS316 as control) for flow rates of 3 and 10 g/s and inlet milk temperatures of 40 and 60 °C. The percent error for the decrease in outlet milk temperatures between the experimental data and computed results was between 2% and 18% except for CNT (29.2%). The calculations of deposit amount for each test case and the surfaces tested were in good agreement with the experiments, i.e., average percent difference values between measured and calculated values were from 11.1% to 38.1% (except CNT) with overall average of 21.5%.     

The effects of modified atmosphere gas composition on microbiological criteria, color and oxidation values of minced beef meat

This paper reports the effects of modified atmosphere gas compositions with different concentrations of CO(2)/O(2)/N(2) on color properties (L*, a* and b* values), oxidation stability (TBARS value) and microbiological properties of minced beef meat stored at +4 °C. Sampling was carried out on the 1st, 3rd, 5th, 7th, 9th, 11th and 14th day of storage. The gas mixtures used were as follows: (i) %30O(2) + %70CO(2) (MAP1), (ii) %50O(2) + %50CO(2) (MAP2), (iii) %70O(2) + %30CO(2) (MAP3), (iv) %50O(2) + %30CO(2) + %20N(2) (MAP4), and (v) %30O(2) + %30CO(2) + %40N(2) (MAP5). Control samples (AP) were packaged under atmospheric air. Pseudomonas, lactic acid bacteria, Brochothrix thermosphacta, and Enterobacteriaceae members were monitored. Among these five modified atmosphere gas compositions, the best preservation for minced beef meat was in MAP4 gas combination maintaining acceptable color together with oxidation stability and acceptable microbial loads until the end of storage period of fourteen days.