Modelling and analysis of abrasive water jet cut surface topography

In this paper, a new approach proposed for modelling the three-dimensional (3D) topography produced on abrasive water jet (AWJ) cut surface is presented. It makes use of the trajectory of jet, predicted from the theory of ballistics and Bitter’s theory of erosion for material removal, for numerically simulating the cutting front. The 2D topography at different depths of the cut surface is generated by considering the trajectories on the cutting front and the abrasive particles impacting the walls of cut surface randomly. For realistic generation of topography on cut surfaces, several instantaneous profiles generated in each region of cut are superimposed to obtain an effective profile. The nature of effective profiles thus predicted is analyzed and validated using power spectral density analysis. The effective profiles predicted at different depths are in turn used to generate the 3D topography of AWJ cut surface. Results obtained with the proposed model are validated with the experimental results.     

The Effect of a Sustained High-Fat Diet on the Metabolism of White and Brown Adipose Tissue and Its Impact on Insulin Resistance: A Selected Time Point Cross-Sectional Study

(1) Background: studies on the long-term dynamic changes in fat depot metabolism in response to a high-fat diet (HFD) on hepatic lipid deposition and insulin resistance are sparse. This study investigated the dynamic changes produced by HFD and the production of dysfunctional fat depots on insulin resistance and liver lipid metabolism. (2) Methods: mice fed a chow or HFD (45% kcal fat) diet had three fat depots, liver, and blood collected at 6, 10, 20, and 30 weeks. Anthropometric changes and gene markers for adipogenesis, thermogenesis, ECM remodeling, inflammation, and tissue insulin resistance were measured. (3) Results: early responses to the HFD were increased body weight, minor deposition of lipid in liver, increased adipocyte size, and adipogenesis. Later changes were dysfunctional adipose depots, increased liver fat, insulin resistance (shown by changes in ITT) accompanied by increased inflammatory markers, increased fibrosis (fibrosis > 2-fold, p < 0.05 from week 6), and the presence of crown cells in white fat depots. Later, changes did not increase thermogenic markers in response to the increased calories and decreased UCP1 and PRDM16 proteins in WAT. (4) Conclusions: HFD feeding initially increased adipocyte diameter and number, but later changes caused adipose depots to become dysfunctional, restricting adipose tissue expansion, changing the brown/beige ratios in adipose depots, and causing ectopic lipid deposition and insulin resistance.     

Influence of Pd Precursor and Method of Preparation on Hydrodechlorination Activity of Alumina Supported Palladium Catalysts

A series of alumina supported Pd catalysts were prepared by the novel deposition-precipitation method adopting the chloride precursor (DP-Cl) of Pd and varying the metal content from 0.25 to 1.0 wt%. The catalytic properties of prepared catalysts were studied by various characterization techniques such as N₂ adsorption, CO chemisorption, TPR, XRD, XPS, and TEM techniques. The activity and stability of the catalysts were evaluated for the gas phase hydrodechlorination (HDC) of chlorobenzene operating at atmospheric pressure. At 1 wt% of Pd the catalyst showed higher chlorobenzene conversion with good stability when tested for a period of 25 h, whereas the other catalysts exhibited a loss in activity with time. In order to elucidate the exceptional activity and stability of this catalyst, a few more catalysts with 1 wt% Pd were prepared by impregnation technique and also using a non-chloride precursor, palladium nitrate. The 1 wt% DP-Cl catalyst again was found to be the best among the others. The activity and stability of the DP-Cl catalyst was also found to be superior to two low-dispersed catalysts, each with 10 wt% Pd, prepared by conventional impregnation method using the chloride and nitrate as the precursors. The characterization results reveal that the high activity and stability of the DP-Cl catalyst is related to the formation of electron deficient Pd species and its stabilization in the octahedral vacancies of alumina.     

Multi-objective optimization of industrial styrene reactor: Adiabatic and pseudo-isothermal operation

Multi-objective differential evolution (MODE) is used to optimize an industrial styrene reactor considering productivity, selectivity and yield as the main objectives. Two reactor configurations (single bed adiabatic operation and steam injected pseudo-isothermal operation) and four combinations of objectives consisting of 5 and 7 variables respectively are considered. Pareto optimal solutions are obtained for all combinations of objective functions for both the configurations. The results are compared with those reported in the literature and an industrial operating point. For all the cases considered, MODE is able to give a Pareto front better (in terms of wider range and a better spread) than that obtained using NSGA for both the configurations. Steam injected reactor configuration is better than the adiabatic reactor configuration in terms of performance. The Pareto optimal solutions obtained from such studies provide a wide range of optimal operating conditions from which an appropriate operating point can be selected based on the requirements of the decision maker.     

Effect of modified layered silicates on the confined crystalline morphology and thermomechanical properties of poly(ethylene oxide) nanocomposites

In this work, poly(ethylene oxide) (PEO)/organoclay nanocomposites with three different types of nanoclays (Cloisite 30B, Somasif JAD400, and Somasif JAD230) were prepared by melt mixing with a laboratory kneader followed by compression molding. The nanocomposites were characterized by atomic force microscopy and scanning electron microscopy. Their crystallization behavior on a hot stage was investigated with polarized optical microscopy. The size and regularity of the spherulites of the PEO matrix were altered significantly by the incorporation of Cloisite 30B, but there was not as much variation with the other two clays. The dynamic viscoelastic behavior of the PEO/organoclay nanocomposites was assessed with a strain‐controlled parallel‐plate rheometer. The effects of clay modification on the thermomechanical and rheological properties were addressed. The reinforcing effect of the organoclay was determined with dynamic mechanical analysis and tensile testing. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Novel thermo‐responsive semi‐interpenetrating network microspheres of gellan gum‐poly(N‐isopropylacrylamide) for controlled release of atenolol

Thermoresponsive microspheres of gellan gum‐poly(N‐isopropylacrylamide), i.e., GG‐P(NIPAAm) semi‐interpenetrating polymer networks (semi‐IPNs) have been prepared by ionic crosslinking and used to study the controlled release (CR) of atenolol (ATL), an antihypertensive drug. Interaction of the drug with polymers was studied by Fourier transform infrared (FTIR) spectroscopy. Differential scanning calorimetry (DSC) was used to confirm the polymorphism and molecular level dispersion of ATL. Scanning electron microscopy (SEM) indicated spherical nature and smooth surfaces of the microspheres with some debris attached on their surfaces. Mean particle size measured by laser light diffraction ranged between 34 and 76 μm. Equilibrium swelling performed at 25°C and 37°C in pH 7.4 phosphate buffer exhibited thermoresponsive nature of the polymers. In vitro drug release performed at 25°C and 37°C indicated temperature‐dependency of ATL release, which was extended up to 12 h. In vitro release profiles at both the temperatures confirmed thermoresponsive nature of the polymers giving pulsatile trends. The % cumulative release data have been fitted to an empirical equation to estimate transport parameters and to understand the nature of drug release. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Carbon-based TiO2-x heterostructure nanocomposites for enhanced photocatalytic degradation of dye molecules

Application of brown titanium dioxide (TiO_2-x) and its modified composite forms in the photocatalytic decomposition of organic pollutants in the environment is a promising way to provide solutions for environmental redemption. Herein, we report the synthesis of effective and stable TiO_2-x nanoparticles with g-C₃N₄, RGO, and multiwalled carbon nanotubes (CNTs) using a simple hydrothermal method. Among all the as-synthesized samples, excellent photocatalytic degradation activity was observed for RGO-TiO_2-x nanocomposite with high rate constants of 0.075 min^?1_, 0.083 min^?1 and 0.093 min^?1 for methylene blue, rhodamine-B, and rosebengal dyes under UV–Visible light irradiation, respectively. The altered bandgap (1.8 eV) and the large surface area of RGO-TiO_2-x nanocomposite impacts on both absorption of visible light and efficiency of photogenerated charge electron (e^?)/hole (h⁺) pair separation. This resulted in enhanced photocatalytic property of carbon-based TiO_2-x nanocomposites. A systematic study on the influence of different carbon nanostructures on the photocatalytic activity of brown TiO_2-x is carried out.     

Morphological exploration of chemical vapor–deposited P-doped ZnO nanorods for efficient photoelectrochemical water splitting

Photoelectrochemical (PEC) water splitting is beneficial and has received attractive attention due to a greater potential to generate hydrogen and oxygen from water by using plentiful solar light to solve the problem of energy crisis. Various active semiconductor materials are used in PEC water splitting applications. Nevertheless, in past decades, most of the researchers suggested that titanium oxide (TiO₂) is the best photoanode for this type of applications. Now, Zinc oxide (ZnO) is considered a perfect substitution to TiO₂ due to its comparable energy band structure and superior photogenerated electron transfer rate. In this study, bare and phosphorous-doped ZnO nanorods were successfully developed on fluorine-doped tin oxide-coated glass (FTO) substrate by chemical vapor deposition. X-ray diffraction (XRD) pattern authenticated hexagonal structure formation with strong diffraction peak of (101), which showed that ZnO nanorods were perfectly developed along c axis. The optical and morphological properties were analyzed by UV–Vis and scanning electron microscopy images. The energy-dispersive X-ray spectra demonstrated that doping agent phosphorous was present in ZnO nanorods. The PEC properties of the developed ZnO nanorods were further investigated and obtained results suggested that a small amount of phosphorous-doped ZnO nanorods enhances their PEC performance.     

Artificial Intelligence System Approach for Optimization of Drilling Parameters of Glass-Carbon Fiber/Polymer Composites

Silicon - In recent times, the study on machining characteristics of combined (hybrid) fiber polymer composites has drawn a remarkable research attention because of its emerging industrial...     

Up-cycling of PET (polyethylene terephthalate) to the biodegradable plastic PHA (polyhydroxyalkanoate)

The conversion of the petrochemical polymer polyethylene terephthalate (PET) to a biodegradable plastic polyhydroxyal-kanoate (PHA) is described here. PET was pyrolised at 450 degrees C resulting in the production of a solid, liquid, and gaseous fraction. The liquid and gaseous fractions were burnt for energy recovery, whereas the solid fraction terephthalic acid (TA) was used as the feedstock for bacterial production of PHA. Strains previously reported to grow on TA were unable to accumulate PHA. We therefore isolated bacteria from soil exposed to PET granules at a PET bottle processing plant From the 32 strains isolated, three strains capable of accumulation of medium chain length PHA (mclPHA) from TA as a sole source of carbon and energy were selected for further study. These isolates were identified using 16S rDNA techniques as P. putida (GO16), P. putida (GO19), and P. frederiksbergensis (GO23). P. putida GO16 and GO19 accumulate PHA composed predominantly of a 3-hydroxydecanoic acid monomer while P. frederiksbergensis GO23 accumulates 3-hydroxydecanoic acid as the predominant monomer with increased amounts of 3-hydroxydodecanoic acid and 3-hydroxydodecenoic acid compared to the other two strains. PHA was detected in all three strains when nitrogen depleted below detectable levels in the growth medium. Strains GO16 and GO19 accumulate PHA at a maximal rate of approximately 8.4 mg PHA/l/h for 12 h before the rate of PHA accumulation decreased dramatically. Strain GO23 accumulates PHA at a lower maximal rate of 4.4 mg PHA/l/h but there was no slow down in the rate of PHA accumulation over time. Each of the PHA polymers is a thermoplastic with the onset of thermal degradation occurring around 308 degrees C with the complete degradation occurring by 370 degrees C. The molecular weight ranged from 74 to 123 kDa. X-ray diffraction indicated crystallinity of the order of 18-31%. Thermal analysis shows a low glass transition (-53 degrees C) with a broad melting endotherm between 0 and 45 degrees C.