Decomposition of 1,2‐dichloroethane in an RF plasma environment

A radio frequency (RF) plasma system has been used to decompose 1,2‐dichloroethane (DCE). Final products were identified by a Fourier transform infrared (FTIR) spectrometer. The main products of DCE decomposition in O₂/Ar plasma were CO₂, CO, and HCl. Other minor chlorinated products were CCl₄, C₂HCl₃, C₂H₃Cl, C₂Cl₄, CHCl₃, C₂HCl₅, and COCl₂. Nonchlorinated products were C₂H₂, C₂H₄, C₂H₆, and HCOOH. The plasma reactor with a brass electrode had a higher decomposition fraction of DCE [η, (C_in ? C_out)/C_in × 100%] than that obtained with other materials (Au, Ni, and Cr). Different electrode configurations (inner and outer) were also evaluated for the decomposition of DCE. Argon plus oxygen was found to be the most suitable carrier/auxiliary gas for DCE decomposition. In addition, operational parameters for DCE decomposition in RF plasma including concentration, operational pressure, and total gas flow rate were evaluated. Copyright © 2003 Society of Chemical Industry     

Oligomeric Composition of Polyols From Fatty Acid Methyl Ester: The Effect of Ring‐Opening Reactants of Epoxide Groups

Commercial availability of fatty acid methyl ester (FAME) from palm oil targeted for biodiesel offers a good feedstock for the production of structurally well‐defined polyols for polyurethane applications. The effect of molecular weight (MW), odd and even carbon numbers, and the linear and branched structure reactants used in the ring‐opening reaction of epoxidized fatty acid methyl ester (E‐FAME) on the properties of polyols was investigated. Conversions of E‐FAME to PolyFAME polyols were confirmed by Fourier transform infrared analysis, oxirane oxygen content, and hydroxyl number. Gel permeation chromatography (GPC) calibrated against polyether polyols as a standard and vapor pressure osmometry were used for MW determination. GPC chromatograms of PolyFAME polyols clearly demonstrated the formation of oligomers during ring‐opening reactions. MW, and odd and even carbon numbers in a structure of linear diols and branched diol used in the syntheses of PolyFAME polyols did not have an effect on crystallinity, glass transition, or melt temperatures measured using Differential scanning calorimetry (DSC). PolyFAME polyols ring‐opened with water, methanol, and 1,2‐propanediol contained secondary hydroxyl groups, whereas PolyFAME polyols ring‐opened with linear diols contained a mixture of primary and secondary hydroxyl groups. It was found that the concentration of primary hydroxyl groups increased significantly by increasing the number of carbons from C2 to C3 in the linear diols. The viscosity of PolyFAME polyols also increased with the MW of linear diols used in the E‐FAME ring‐opening reaction. These findings would be beneficial for formulators in choosing the most cost effective polyols for polyurethane formulations.     

Physicochemical stability of calcium alginate beads immobilizing TiO2 nanoparticles for removal of cationic dye under UV irradiation

Recently, there have been considerable interests to immobilize photocatalyst in alginate beads for removing pollutants from water sources. However, the feasibility of using alginate beads in industry largely depends on its long‐term stability during operation. This study investigated the physicochemical stability of alginate/titanium dioxide beads (Alg/TiO₂) when exposed to UV irradiation in aqueous environment. The degradation of Alg/TiO₂ beads was evident because the diameter and mass of the beads was reduced by 12% and 40%, respectively, after 120 h of irradiation. A substantial amount of TiO₂ was leached into the external medium. Consequently, the removal efficiency of model cationic dye was found to reduce after every process cycle. Morphological analysis showed the formation of cavities on the surface of the Alg/TiO₂ beads. Interestingly, the blank alginate beads degraded more rapidly than the Alg/TiO₂ beads, confirming the UV‐shielding effect of TiO₂. Nevertheless, this study reveals the need to improve the UV stability of alginate‐based beads before they can be considered for practical application. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45002.     

Robust Red Organic Nanoparticles for In Vivo Fluorescence Imaging of Cancer Cell Progression in Xenografted Zebrafish

Bright and red‐emissive organic nanoparticles (NPs) are demonstrated as promising for in vivo fluorescence imaging. However, most red organic dyes show greatly weakened or quenched emission in the aggregated state. In this work, a robust red fluorophore (t‐BPITBT‐TPE) with strong aggregate‐state photoluminescence and good biocompatibility is presented. The NPs comprised of t‐BPITBT‐TPE aggregates encapsulated within 1,2‐distearoyl‐sn‐glycero‐3‐phosphoethanolamine‐N‐[methoxy(polyethylene glycol) (DSPE‐mPEG) micelles exhibit a photoluminescence peak at 660 nm with a high fluorescence quantum yield of 32% in aqueous media. The NPs can be facilely charged by using the same polymeric matrix with different terminal groups, e.g., methoxy (DSPE‐mPEG), amine (DSPE‐PEG‐NH₂), or carboxymethyl (DSPE‐PEG‐COOH) groups. The biocompatibility, toxicity, circulation, and biodistribution of the NPs are assessed using the zebrafish model through whole embryo soaking and intravenous delivery. Furthermore, HeLa and MCF‐7 cells tagged with t‐BPITBT‐TPE in DSPE‐PEG‐NH₂‐TAT polymer NPs are xenografted into zebrafish larvae to successfully track the cancer cell proliferation and metastasis, demonstrating that these new NPs are efficient cancer cell trackers. In addition, the NPs also show good in vivo imaging ability toward 4T1 tumors in xenografted BALB/c mice.     

Effect of dietary methylmercury and seleno-methionine on Sacramento splittail larvae

The effects of methylmercury (MeHg) and selenium (Se) contamination on food webs in the San Francisco Estuary have received considerable attention during the past decade. However, knowledge of their effects on native fishes of California is lacking. This study investigated the interactive effects of dietary MeHg and seleno-methionine (SeMet) on Sacramento splittail (Pogonichthys macrolepidotus) larvae. Twelve diets containing increasing levels of SeMet (0.64, 8.2 and 35.0 microg Se g(-1) diet) and MeHg (0.01, 0.13, 4.7 and 11.7 microg Hg g(-1) diet) were fed to 21-day post-hatch larvae for 4 weeks in 2-L beakers at 25 degrees C. Fish were fed twice a day at a feeding rate of 40, 30, 25 and 20% of body weight during the 1st, 2nd, 3rd and 4th week, respectively. At the end of week 4, no significant difference (P>0.05) was observed among treatments for mortality, body length or weight, and condition factor. Bioaccumulation of Hg and Se responded positively and significantly (P<0.05) to their dietary concentrations. The molar ratio of Se/Hg in diets was linearly correlated to the ratio of Se/Hg in fish. Dietary Se inhibited Hg accumulation, which was negatively correlated to the dietary Se/Hg ratio. Histopathological examination revealed severe gill anomaly and liver glycogen depletion in fish fed the 11.7 microg Hg g(-1) diet. Liver glycogen depletion and kidney tubular dilation were found in larvae fed the 11.7 microg Hg and 11.7 microg Hg+35 microg Se g(-1) diets. In conclusion, dietary Hg enhanced Se accumulation but dietary Se inhibited Hg accumulation in splittail. Dietary Se showed a protective effect in fish fed the high MeHg diet. This protection was related to the dietary Se/Hg ratio, which is a more reliable criterion for evaluating the interactive effect between Se and Hg in splittail.     

A bipolar output voltage pulse transformer boost converter with charge pump assisted shunt regulator for thermoelectric energy harvesting

This system presents an energy harvesting system that generates bipolar output voltage (±1 V) based on a miniature 1:1 turn-ratio pulse transformer boost converter using sub-threshold level input voltage source. A shunt regulator is designed using six-transistor Schmitt-Trigger core to limit the boost converter output voltage. Another power stage, i.e. a fully integrated on-chip single-stage cross-coupled charge pump, then generates 3 V output from the unused extra output power of boost converter, which is shunted otherwise. The increased voltage headroom generated is instrumental for sensor, analog and RF circuits. Charge pump clock frequency is designed to adaptively tracking the input voltage, which is sensed using power-saving time-domain digital technique. Based on a standard CMOS 0.13-µm technology, chip measurement verified the operations of the boost converter, shunt regulator and bipolar charge pump prototypes, respectively. Simulations confirmed the full system operations. During start-up, the system only requires minimum start-up input voltage of 36 mV at input power of 5.8 µW.     

Performance analysis of an FFH/BFSK product-combining receiverunder multitone jamming

The performance of a fast frequency-hopped binary frequency-shift keying (FFH/BFSK) spread-spectrum (SS) communication system is studied in this paper. The FFH system employs a product-combining receiver against the worst case multitone jamming (MTJ) and additive white Gaussian noise (AWGN). The compact characteristic functions of the natural logarithm of the product-combiner outputs are obtained based on the Taylor series expansion. The characteristic functions are then used to derive the bit error rate (BER) expressions that are applicable to higher diversity levels. Our analysis, validated by the simulation results, shows that the band MTJ is generally more harmful than the corresponding independent MTJ. The BER performance of the product-combining receiver is shown to possess good MTJ rejection capability compared to that of the soft-decision linear-combining receiver, especially under both moderate and strong MTJ power conditions     

Studies on miscibility of uncompatibilized nylon 66–santoprene blends

This article investigates the miscibility of nylon 66 and santoprene blends. The nylon 66–santoprene was blended to give the following compositions: 100/0, 90/10, 75/25, 50/50, 25/75, and 0/100. No compatibilizer was used during blending of the two components. Thermal properties and morphology of the blends were checked by using differential scanning calorimetry and scanning electron microscopy (SEM). The effect of blend composition on the mechanical properties was checked through tensile and izod impact tests. Both components were immiscible, as confirmed by double melting temperature, corresponding to that of polypropylene component in santoprene and nylon 66. Also, the melting temperature of nylon was not significantly affected by blending it with santoprene. However, the crystallization temperature of nylon increased after blending. This was attributted to the ethylene–propylene–diene monomer content in santoprene, which acts as a nucleating agent. The effect of blend composition on mechanical properties occurred at the 50/50 composition and above. Evidence of immiscibility of both components was also confirmed by the presence of a two-phase structure, as revealed by SEM. © 1998 John Wiley & Sons, Inc. J Appl Polm Sci 68: 1285–1295, 1998     

ELTD1 Activation Induces an Endothelial-EMT Transition to a Myofibroblast Phenotype

ELTD1 is expressed in endothelial and vascular smooth muscle cells and has a role in angiogenesis. It has been classified as an adhesion GPCR, but as yet, no ligand has been identified and its function remains unknown. To establish its role, ELTD1 was overexpressed in endothelial cells. Expression and consequently ligand independent activation of ELTD1 results in endothelial-mesenchymal transistion (EndMT) with a loss of cell-cell contact, formation of stress fibres and mature focal adhesions and an increased expression of smooth muscle actin. The effect was pro-angiogenic, increasing Matrigel network formation and endothelial sprouting. RNA-Seq analysis after the cells had undergone EndMT revealed large increases in chemokines and cytokines involved in regulating immune response. Gene set enrichment analysis of the data identified a number of pathways involved in myofibroblast biology suggesting that the endothelial cells had undergone a type II EMT. This type of EMT is involved in wound repair and is closely associated with inflammation implicating ELTD1 in these processes.