机动车三元催化剂结构性能的研究

当前治理汽车尾气污染的最好方法是采用含有贵金属的三元催化剂同时对NOx、HC、CO进行处理。催化转化器的结构性能直接影响催化效率的高低,准确测定及鉴定催化剂中主要部件的结构性能指标就具有重要意义。该文利用X-射线衍射光谱仪(XRD)、扫描电子显微镜能谱分析技术(SEM-EDS)以及等温液氮吸附-脱附技术对6种使用过的和未使用过的机动车尾气三元催化剂的结构性能进行分析研究。结果表明:可以通过X-射线衍射光谱仪区分各催化剂载体的材质,文中样品经鉴定都为堇青石陶瓷蜂窝载体,不同催化剂的比表面积和孔容存在差异;通过扫描电子显微镜可以观察到催化剂载体表面涂层的微观结构,及一些催化剂载体表面涂层出现的裂纹;通过能谱分析各载体主要元素的大致含量。

Extraction of nickel from molybdenum leaching residue of metalliferous black shale by segregation roasting and acid leaching

The recovery of nickel from molybdenum leach residue by the process of segregation roasting-sulfuric acid leaching-solvent extraction was investigated. The residue was characterized by microscopic investigations, using X-ray fluorescence spectrometry （XRF） and X-ray diffractometry （XRD） techniques and the residue after segregation roasting was characterized by chemical phase analysis method. A series of experiments were conducted to examine the mass ratio of activated carbon （AC） to the residue, segregation roasting time and temperature, sulfuric acid concentration, liquid-to-solid ratio, leaching time, leaching temperature, addition amount of 30% H2O2, stirring speed （a constant） on the leaching efficiency of nickel. A maximum nickel leaching efficiency of 90.5% is achieved with the mass ratio of AC to the residue of 1：2.5, segregation roasting time of 2 h, segregation roasting temperature of 850 ℃, sulfuric acid concentration of 4.5 mol/L, liquid-to-solid ratio of 6：1, leaching time of 5 h, leaching temperature of 80 ℃, addition of 30% H202 of 0.6 mL for 1 g dry residue. Under these optimized conditions, the average leaching efficiency of nickel is 89.3%. The nickel extraction efficiency in the examined conditions is about 99.6%, and the nickel stripping efficiency in the examined conditions is about 99.2%.

Study on Structure and Crystallinity of A New Biodegradable Aliphatic-Aromatic Copolyester

A series of biodegradable aliphatic-aromatic copolyesters, poly(butylene terephthalate-co-butylene adipate-co- ethylene terephthalate-co-ethylene adipate) (PBATE), were synthesized from terephthalic acid (PTA), adipic acid (AA), 1,4-butanediol (BG) and ethylene glycol (EG) through direct esterification and polycondensation. The sequence structure and crystallinity of the copolyester were investigated by 1H NMR spectroscopy and the wide-angle X-ray diffractometry (WAXD). The analytical results showed that the PBATE copolyester was a random copolymer and the composition of PBATE copolyester was almost consistent with the feed molar ratios. The crystal structure of PBATE copolyester belonged to the triclinic crystalline system; The variation in melting point of the synthesized PBATE copolyester agreed well with the estimation obtained by the Flory equation and was applicable to the random copolymer.

Towards full repair of defects in reduced graphene oxide films by two-step graphitization

The complete restoration of a perfect carbon lattice has been a central issue in the research on graphene derived from graphite oxide since this preparation route was first proposed several years ago, but such a goal has so far remained elusive. Here, we demonstrate that the highly defective structure of reduced graphene oxide sheets assembled into free-standing, paper-like films can be fully repaired by means of high temperature annealing （graphitization）. Characterization of the films by X-ray photoelectron and Raman spectroscopy, X-ray diffraction and scanning tunneling microscopy indicated that the main stages in the transformation of the films were （i） complete removal of oxygen functional groups and generation of atomic vacancies （up to 1,500 ~C）, and （ii） vacancy annihilation and coalescence of adjacent overlapping sheets to yield continuous polycrystalline layers （1,800-2,700 ~C） similar to those of highly oriented graphites. The prevailing type of defect in the polycrystalline layers were the grain boundaries separating neighboring domains, which were typically a few hundred nanometers in lateral size, exhibited long-range graphitic order and were virtually free of even atomic-sized defects. The electrical conductivity of the annealed films was as high as 577,000 S-m-1, which is by far the largest value reported to date for any material derived from graphene oxide, and strategies for further improvement without the need to resort to higher annealing temperatures are suggested. Overall, this work opens the prospect of truly achieving a complete restoration of the carbon lattice in graphene oxide materials.

Synthesis and properties of copolymers based on 5,6-dinitrobenzothiadiazole with low band gap and broad absorption spectra

One polythiophene derivative PT3T and two low band gap copolymers,PBTT-T3T and PBTT,with different ratios of 5,6-dini-trobenzothiadiazole as the acceptor unit in the polymer backbone have been synthesized by Pd-catalyzed Stille-coupling polymerizations.Thermal stability,X-ray diffraction analyses,UV-vis absorption spectra,photoluminescence spectra and electrochemical properties of the copolymers were investigated.The band gap estimated from UV-vis-NIR spectra of the copolymers films varied from 1.39 to 1.94 eV.Among these copolymers,the films of PBTT-T3T and PBTT,which contain the 5,6-dinitrobenzothiadiazole unit,cover a broad wavelength range in the visible and near-infrared region from 400 to 1000 nm with the maximal peak absorption around 700 nm,which is exactly matched with the maximum in the photon flux of the sun.

Fabrication of single-crystalline ZnSe multipod-based structures

ZnSe multipod-based structures,including tetrapod-like microrods,long microwires,and short nanorods,are selectively prepared by atmospheric pressure thermal evaporation of ZnSe nanoparticles without using any catalyst.The morphologies could be well controlled by simply adjusting the deposition position.The phase structures,morphologies,and optical properties of the products are investigated by X-ray diffraction(XRD),scanning electron microscopy(SEM),high-resolution transmission electron microscopy(TEM),and photoluminescence(PL) spectroscopy.A vapor-liquid mechanism is proposed for the formation of ZnSe multipod-based structures.The presented route is expected to be applied to the synthesis of other Ⅱ-Ⅵ groups or other group's semiconductor materials with controllable morphologies.