Ethanol steam reforming over Ni/ZSM-5 nanosheet for hydrogen production

Compared to reforming reactions using hydrocarbons,ethanol steam reforming(ESR)is a sustainable alternative for hydrogen(H_(2))production since ethanol can be produced sustainably using biomass.This work explores the catalyst design strategies for preparing the Ni supported on ZSM-5 zeolite catalysts to promote ESR.Specifically,two-dimensional ZSM-5 nanosheet and conventional ZSM-5 crystal were used as the catalyst carriers and two synthesis strategies,i.e.,in situ encapsulation and wet impregnation method,were employed to prepare the catalysts.Based on the comparative characterization of the catalysts and comparative catalytic assessments,it was found that the combination of the in situ encapsulation synthesis and the ZSM-5 nanosheet carrier was the effective strategy to develop catalysts for promoting H_(2) production via ESR due to the improved mass transfer(through the 2-D structure of ZSM-5 nanosheet)and formation of confined small Ni nanoparticles(resulted via the in situ encapsulation synthesis).In addition,the resulting ZSM-5 nanosheet supported Ni catalyst also showed high Ni dispersion and high accessibility to Ni sites by the reactants,being able to improve the activity and stability of catalysts and suppress metal sintering and coking during ESR at high reaction temperatures.Thus,the Ni supported on ZSM-5 nanosheet catalyst prepared by encapsulation showed the stable performance with~88% ethanol conversion and~65% H_(2) yield achieved during a 48-h longevity test at 550-C.

SYNTHESIS OF STYRENIC TONER PARTICLES BY SPG EMULSIFICATION TECHNIQUE

This research studied the initiator efficiency for producing polymeric particles of poly(styrene-co-methyl methacrylate)copolymers by a Shirasu porous glass membrane(SPG)emulsification technique followed by suspension copolymerization.BPO,ADVN,and AIBN were used as initiators and we found that BPO is the most suitable initiator.Copolymers for various feed ratios of styrene/methyl methacrylate were thus synthesized by benzoyl peroxide,and their copolymer particle size,molecular weight distribution and pat-ride size distribution were characterized.Then n-BMA or 2-EHMA was added as the third monomer to decrease the terpolymer glass transition temperature.This article describes the preparation technique,recipes and polymerization conditions for producing both copolymer and terpolymer particles,particle size changes,the corresponding particle morphologies and glass transition temperatures.

Extraction of Palladium from Acidic Chloride Media into Emulsion Liquid Membranes using LIX 984N-C^®

The extraction of palladium from hydrochloric acid solutions into emulsion liquid membranes (ELMs) using LIX 984N-C as the extractant was investigated. The influential factors and the total capacities of palladium extraction were determined by a batch method. The behavior of palladium extraction by ELMs under the operational conditions-pH of the external feed phase, surfactant and extractant concentration, internal stripping phase concentration, treat ratio and agitation speed were reported. Using LIX 984N-C, palladium was effectively extracted from the external acidic chloride feed phase into the internal receiving phase of W/O emulsions. More than 92% of palladium could be extracted at a feed pH of 2 with 3% Span 80, 9% LIX 984N-C and 7M HCl at a stirring speed of 300 rpm.

Mixed metal oxide catalysts for the selective oxidation of ethylbenzene to acetophenone

MgAl and MgMAl oxides（M = Co,Ni and Cu） with a Mg：M：Al molar ratio = 4：1：1 were synthesized from the calcination of their corresponding layered double hydroxide（LDHs） precursors.Their catalytic activities were examined for the oxidation of ethylbenzene using tert-butylhydroperoxide（TBHP） as an oxidant.The oxidized product was mainly acetophenone.The catalytic activities were in the order of MgCuAlMgNiAl～NiAl～MgCoAl～CoAlCuAlMgAl oxides.Reusability studies show that the catalysts are stable under the reaction conditions.

Flame-Retarding Epoxy Resin Films by Curing with Organophosphorus Containing Diamine

An organophosphorus-based diamine has been synthesized and used as a curing and flame retarding bifunctional agent for epoxy resins.This phosphorodiamidate functions not only as a crosslinking materials in the Epon 828 epoxy resin curing process but also as a fire retarding compound to produce thin films or composites upon curing.This phosphorus-containing reactive amine was synthesized via condensation of phenyphosphonic dichloride with ethylenediamine in the presence of sodium methoxide.The product was then purified and later characterized by NMR and FTIR spectroscopy as well as MALDI-TOF mass spectrometry.Kinetics studies of the curing reaction of the phosphorodiamidate were carried out in comparison with the non-phosphorus containing ethylenediamine reference crosslinking agent.Thermal stability of the cured epoxy ware investigated by thermogravimetric analysis(TGA)and differential scanning calorimetry(DSC).Moreover,flame retardant properties of the obtained materials was investigated by limiting oxygen index(LOI)measurements as well as the UL-40 method.The obtained results show that epoxy resin cured with phosphorodiamidate possesses higher thermostability compared to the epoxy cured with the regular ethylenediamine counterpart.This is evident by higher amount of char formed upon burning.More importantly,the LOI value of 27 was observed in the phosphorodiamidate-cured epoxy resin compared with LOI of 20 of the epoxy resin cured with ethylenediamine where no phosphorus was present.The UL-94 highest rating of V-0 materials was obtained with only about 2-3 wt%of the phosphorus element.The chemistry,curing kinetics,and thermal properties of these new epoxy formulations are discussed.

Conductive Poly(3-methylthiophene) Thin Films

The work described herein represents an efficient method in the deposition of poly(3-methylthiophene),P3MeTh,thin films utilizing a microwave plasma system in combination with a simultaneous doping with iodine.It was envisaged that,an alternative poly(3-methylthiophene),P(3MeTh),with an electron donating methyl substituent,would reduce the degree of ring opening which reportedly occur to a certain extent during the plasma polymerization process of its parent compound polythiophene.An alkyl substituent would also increase the solubility of the materials.P(3MeTh)thin film deposition has been performed utilizing microwave-induced plasma polymerization in order to directly grow films on glass substrates.Moreover,simultaneous doping of the so-formed polymer with iodine has been carried out as opposed to the post-synthesis doping method.This is aimed to prolong electrical conducting lifetime of the materials.The synthesized films were characterized by attenuated total reflection fourier transform infrared(ATR FT-IR)spectroscopy and energy dispersive X-ray spectroscopy(EDS)to confirm the incorporation of iodine dopant into the films.Scanning electron microscopy showed uniformly deposited films.It has been observed that the electrical conductivity of the doped film is 2 orders of magnitude higher than the undoped counterpart.The doped fabricated films exhibited UV-vis spectra indicative of increased π-conjugation(536 nm).Furthermore,electrical conductivity of the in situ doped P(3MeTh)is more highly sustained over a longer period of time.