THE SYNTHESIS OF MODIFIED DIPHENYL OXIDE RESIN

Modified diphenyl oxide resin was synthesized by co-polymerization of unsaturated acid and diphenyl oxide derivants. And then modified bismaleimide resin and expoxide linear phenolic resin were added into modified diphenyl oxide resin to co-polymerize and modify once more. The system was applied in composites. Their properties were investigated and found that they met the requirements as a heat-resisting adhesive.

Ionic liquids-SBA-15 hybrid catalysts for highly efficient and solvent-free synthesis of diphenyl carbonate

Diphenyl carbonate(DPC)is one of the versatile carbonates,and is often used for the production of polycarbonates.In recent years,the catalytic synthesis of DPC has become an important topic but the development of a highly active metal-free catalyst is a great challenge.Herein,a series of ionic liquids-SBA-15 hybrid catalysts with different functional groups have been developed for the synthesis of DPC under solventfree condition,which are effective and clean instead of the metal-containing catalysts.It is found that in the presence of[SBA-15-IL-OH]Br catalyst,methyl phenyl carbonate(MPC)conversion of 80.5%along with 99.6%DPC selectivity is achieved,the TOF value is thrice higher than the best value reported by using transition metal-based catalysts.Moreover,the catalyst displays remarkable stability and recyclability.This work provides a new idea to design and prepare eco-friendly catalysts in a broad range of applications for the green synthesis of carbonates.

Molybdenum tailored Co^(0)/Co^(2+)active pairs on a perovskite-type oxide for direct ethanol synthesis from syngas

Selective synthesis of ethanol from syngas under the Co-based catalysts is still challenging due to the hard of regulating the active site Co^(0) and Co^(2+)ratio.In this work,a series of CaTi_(0.9-x)Co_(x)Mo_(0.1)O_(3)(x=0,0.1-0.4)and CaTi_(0.7)Co_(0.3)O_(3) catalysts were prepared by using citric acid complexation method to promote the synthesis of ethanol.It was found that Mo species in the perovskite lattice can regulate the Co^(0) and Co^(2+)ratio through the domain-limiting effect of perovskite and the degree of Co reduction could be adjusted by changing the Co/Mo molar ratio.Among these investigated catalysts,the total selectivity of alcohols over the catalyst with the optimal Co/Mo ratio CaTi_(0.6)Co_(0.3)Mo_(0.1)O_(3) reached 39.1%,with ethanol accounting for 74.7%,which was ascribed to the moderate and tightly bound ratio of dissociative to non-dissociative adsorption sites on the surface and the balance of CH_(x)-CH_(y) coupling and C^(O) insertion.

Microwave-assisted Synthesis of Al_(4)SiC_(4) and Its Effect on Properties of MgO-C Refractories

Al_(4)SiC_(4) was synthesized from Al powder, silicon carbide, and graphite by microwave sintering, and characterized by XRD and SEM. Then the synthesized material was added to the magnesia carbon refractory brick to study its effect on the oxidation resistance, apparent porosity, bulk density, elastic modulus, and modulus of rupture. It is found that Al_(4)SiC_(4) can be synthesized by microwave sintering at 1 300 ℃ and the addition of Al_(4)SiC_(4)-containing material as an antioxidant can enhance the oxidation resistance of the magnesia carbon refractory brick.

Investigation on the deactivation cause of lead-zinc double oxide for the synthesis of diphenyl carbonate by transesterification

The deactivation cause of lead-zinc double oxide for synthesis of diphenyl carbonate （DPC） by transesterification of dimethyl carbonate （DMC） with phenol has been investigated. X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS）, infrared spectroscopy （IR）, thermogravimetry analysis （TG）, atomic absorption spectroscopy and elementary analysis are employed for the catalyst characterization. The results show that, the formation of Pb4O（OC6H5）6 through the reaction of phenol and lead species in the catalyst leads to the crystal phase change of active component and serious leaching of lead, which is the cause of the catalyst deactivation. In addition, the composition of the leached lead is ascertained to be a mixture of Pb4O（OC6H5）6 and PbO with the weight percentage of 62.7% and 37.3%, respectively.

Higher alcohol synthesis over Cu-Fe composite oxides with high selectivity to C_(2+)OH

Cu-Fe composite oxides were prepared by co-precipitation method and tested for higher alcohol synthesis from syngas. The selectivity to C2＋OH and C6＋OH in alcohol distribution was very high while the methane product fraction in hydrocarbon distribution was rather low, demonstrating a promising potential in higher alcohols synthesis from syngas. The distribution of alcohols and hydrocarbons approximately obeyed Anderson-Schulz-Flory distribution with similar chain growth probability, indicating alcohols and hydrocarbons derived from the same intermediates. The effects of Cu/Fe molar ratio, reaction temperature and gas hourly space velocity （GHSV） on catalytic performance were studied in detail. The sample with a Cu/Fe molar ratio of 10/1 exhibited the best catalytic performance. Higher reaction temperature accelerated water-gas-shift reaction and led to lower total alcohols selectivity. GHSV showed great effect on catalytic performance and higher GHSV increased the total alcohol selectivity, indicating there existed visible dehydration reaction of alcohol into hydrocarbon.

Electrocatalytic Synthesis of Propylene Carbonate from CO_2 and Propylene Oxide

The electrocatalytic synthesis of propylene carbonate（PC） from CO2 and propylene oxide（PO） was studied under mild conditions（PCO2=1.01×105 Pa, t=25 ℃）. Influences of solvents, supporting electrolytes, the passed charge, the nature of electrodes and the current density（j） on the yield of PC were investigated to optimize the electrolytic conditions, with the maximal yield to be 46.2%, the selectivity of propylene carbonate is 100%. The reduction of propylene oxide in the absence and presence of CO2 was examined by cyclic voltammetry. The mechanism of the reaction initiated by the synergistic effect of halides ions of supporting electrolytes with nucleophilicity and the metal ions from scarification anode with Lewis acid acidity was proposed on the basis of our results.

Hydrothermal Synthesis and Structure of [CH3NH3]2[(VⅣO)2(VⅤO4)2]:A New Layered Mixed-valence Vanadium Oxide Incorporated with Organic Cations

A new layered mixed valence vanadium oxide, [CH 3NH 3] 2[(V ⅣO) 2(V ⅤO 4) 2], which contains interlamellar organic cations was prepared under hydrothermal conditions and its single crystal structure was determined. It crystallizes in a triclinic system with space group P 1, a =0 625 59(8) nm, b =0 639 84(9) nm, c =0 747 19(10) nm, α =78 718(2)°, β =80 099(2)°, γ =77 100(2). The compound contains mixed valence V 4+ /V 5+ vanadium oxide layers constructed from VO 4 tetrahedra, pairs of edge sharing VO 5 square pyramid and methylamine with protonated organic amines occupying the interlayer space.

Hydrothermal synthesis of vanadium oxide nanotubes by a facile route

Vanadium oxide nanotubes were synthesized by hydrothermal treatment from V2O5·nH2O sols as precursor and dodecylamine as structure-directing template. The morphology and structure of the nanotubes were characterized by SEM, TEM, XRD, TG-DTA and FTIR. The experimental results reveal that the duration of the hydrothermal treatment is of importance for obtaining VOx-NTs which have a layered structure. TG-DTA study indicates that V5+ cations in nanotubes are partially reduced to V4+ cations. The results from FTIR spectra indicate the difference in V-O vibrations between before and after hydrothermal treatment. From the results, it suggests that during hydrothermal treatment, the rearrangement of the vanadium oxide structure leads to the formation of VOx nanotubes from lamellar structure because of the presence of V4+ species.

A circular microreaction method to the safe and efficient synthesis of 3-methylpyridine-N-oxide

3-Methylpyridine-N-oxide is an essential intermediate in the preparation of 2-chloro-5-methylpyridine,which can be used to synthesize nicotine insecticides such as imidacloprid and acetamiprid.The traditional method of production of 3-methylpyridine-N-oxide is catalytic oxidation of 3-methylpyridine in semi-batch reactors.Due to strong exothermic reaction and explosive property of 3-methylpyridine,the reaction efficiency and safety is low using batch technology.Therefore,the development of a safer and efficient 3-methylpyridine-N-oxide production process is very necessary in industrial production.In this paper,microreaction systems were introduced into the preparation of 3-methylpyridine-N-oxide.The comparison of three different methods(traditional semibatch method,co-current microreaction method,and circular microreaction method)showed that the circular microreaction method was the most applicable,with relative higher product yield(~90%),less side reaction and better reaction control.

Microwave synthesis of La_(1-x)Sr_xCo_(1-y)Fe_yO_3 cathode materials for solid oxide fuel cells

La1-xSrxCo1-yFeyO3 cathode materials for solid oxide fuel cells were prepared by the microwave synthesis method.The reaction mechanism was studied using a thermal analysis method.The influences of microwave synthesis conditions were examined and the characteristics of the samples were determined by X-ray diffraction and scanning electron microscopy.It was found that the optimum conditions were the microwave power of 800 W and the reaction time of 40 min.Samples with perosvkite-type crystal structure were obtained.The samples consist of uniformly distributed internal particles and the particle size is less than 1 μm.

Self-assembling Synthesis of Vanadium Oxide Nanotubes and Simple Determination of the Content of V(IV)

High-yielding low-cost vanadium oxide nanotubes were prepared by the hydrothermal self-assembling process from vanadium pentoxide and organic molecules as structure-directing templates.Moreover,a new method was discovered for determining the content of V (IV) in vanadium oxide nanotubes by thermogravimetric analysis (TGA).This method is simple,precise and feasible and can be extended to determine the content of low oxidation state in the other transition metal oxide nanomaterials.

Nanodispersed Oxides-Plasma-Chemical Synthesis and Properties

We discuss the plasma-chemical synthesis and the properties of transition metals oxides, Al2O3, SiO2, rare-earth oxides, oxides for ceramics and metal-ceramics, and oxides used as catalysts. Bearing in mind the indisputable advantages of using plasma-chemically synthesized nanodispersed oxides for the needs of various industrial fields, we set out to review the articles published in the past few years devoted to the problems of plasma-chemical synthesis and characterization of nanodispersed oxides.

Hydrothermal Synthesis, Crystal Structure and Fluorescent Property of a Cd(Ⅱ) Complex Based on Biimidazole and Isonicotinate-N-oxide

A new complex [Cd（H2biim）2（H2O）2]·（ino）2·4H2O （H2biim = 2,2＇-biimidazole, ino = isonicotinate-N-oxide） has been prepared and characterized by single-crystal X-ray diffraction analysis, IR and fluorescence spectra analysis. The crystal is of triclinic system, space group P1 with a = 7.5380（6）, b = 8.0402（7）, c = 13.5094（11） , α = 104.269（1）, β = 93.604（1）, γ = 98.349（1）°, V = 780.93（11） 3, Mr = 765.00, Dc = 1.627 g/cm3, F（000） = 390, μ = 0.776 mm-1 and Z = 1. The final R = 0.0322 and wR = 0.0825 for 7038 observed reflections with I 2σ（I） and R = 0.0341 and wR = 0.0832 for all data. The title complex exhibits an infinite chain-like structure through bridging isonicotinate-N-oxide. Strong interchain hydrogen bonds between isonicotinate-N-oxide and H2biim result in the robust 3-D supramolecular architecture. Moreover, the complex shows strong photoluminescence with emission maximum at λ = 401 nm upon λex = 330 nm.

Chemical synthesis of zinc oxide nanorods for enhanced hydrogen gas sensing

Zinc oxide （ZnO） nanorods are prepared using equimolar solution of zinc nitrate （（Zn（NO3）2） and hexamethylenete- tramine （C6HleN4） by the hydrothermal technique at 80 ~C for 12 h. Epitaxial growth is explored by X-ray diffraction （XRD） patterns, revealing that the ZnO nanorods have a hexagonal （wurtzite） structure. Absorption spectra of ZnO are measured by UV-visible spectrometer. The surface morphology is investigated by field emission scanning electron mi- croscopy （FESEM）. The synthesized ZnO nanorods are used for detecting the 150 ~C hydrogen gas with a concentration over 1000 ppm. The obtained results show a reversible response. The influence of operating temperature on hydrogen gas detecting characteristic of ZnO nanorods is also investigated.

Phytogenic Synthesis of Metal/Metal Oxide Nanoparticles for Degradation of Dyes

Now-a-days nanotechnology is one of the booming fields for the researchers.With the increase in industrialization mainly textile,paper,medicine,plastic industry,there is an increase in concentration of organic dyes as pollutant.Release of harmful dyes in water bodies has become a serious issue,as most of the dyes are carcinogenic and mutagenic in nature and causes various diseases.Therefore,there is a requirement to find out new approaches for efficient treatment of effluent containing dyes.Nanoparticles are one of the potential solutions to this problem.They can be synthesized from different methods,however synthesis of nanoparticles from different plant parts(leaf,root or stem extract)is economical as well as ecofriendly.Phytogenic nanoparticles have various environmental applications and one of them is remediation of dyes.The aim of this review is to provide an overview of last five years studies about catalytic and photocatalytic degradation of various harmful dyes by plant synthesized nanoparticles,mechanism of degradation and advantages and disadvantages of phytogenic synthesis.

CATALYTIC SYNTHESIS OF α-CYANO-α,β-UNSATURATED SULPHONES IN THE PRESENCE OF ORGANOTELLURIUM OXIDE

Using bis(p-methoxyphenyl)telluroxide(BMPTO)as the catalyst, phenylsulphonyl acetonitrile condensed easily with aromatic aldehydes at room temperature to give -cyano- ,β-unsaturated sulphones in high yields.

THE SELECTIVE OXIDATION OF ALCOHOLS-STUDIES ON THE SYNTHESIS AND PROPERTIES OF HEXAHYDROPYRIDINE CHROMIUM TRIOXIDE HYDROCHLORIDE

A new Cr(Vl)complex,hexahydropyridine chromium trioxide hydrochloride is developed.Its behavior and seiectivity on alcohols are investugated

Selective synthesis of nitrate from air using a plasma-driven gas-liquid relay reaction system

The direct oxidation of nitrogen is a potential pathway to achieving the zero-carbon-emission synthesis of nitric acid or nitrate, because it does not involve ammonia synthesis and additional ammonia oxidation processes. However, the slow kinetics of nitrogen oxidation and the difficult selective control of oxidation products hinder the development of this process. In this study, a plasma-driven gas-liquid relay reaction system was developed to overcome these limitations. A typical feature of this reaction system is that it can efficiently generate NO_x under plasma exposure;moreover, the specific anions in the absorption solution can be oxidized to strong oxidants capable of relay oxidation of low-valence nitrogen oxides. This feature allows for the deep oxidation of nitrogen, thus enabling the oxidation products of nitrogen to exist in high-valence states in the absorption solution. For experimental verification, we achieved the 100% selective synthesis of nitrate under plasma exposure, with air as the supply gas and a sodium sulfate solution as the absorption solution.

Water-based synthesis of nanoscale hierarchical metal-organic frameworks:Boosting adsorption and catalytic performance

The combination of nano sizes,large pore sizes and green synthesis is recognized as one of the most crucial and challenging problems in constructing metal-organic frameworks(MOFs).Herein,a water-based strategy is proposed for the synthesis of nanoscale hierarchical MOFs(NH-MOFs)with high crystallinity and excellent stability.This approach allows the morphology and porosity of MOFs to be fine tuned,thereby enabling the nanoscale crystal generation and a well-defined hierarchical system.The aqueous solution facilitates rapid nucleation kinetics,and the introduced modulator acts as a deprotonation agent to accelerate the deprotonation of the organic ligand as well as a structure-directing agent(SDA)to guide the formation of hierarchical networks.The assynthesized NH-MOFs(NH-ZIF-67)were assessed as efficient adsorbents and heterogeneous catalysts to facilitate the diffusion of guest molecules,outperforming the parent microZIF-67.This study focuses on understanding the NH-MOF growth rules,which could allow tailor-designing NH-MOFs for various functions.