提升五号桩油田二氧化碳吞吐效果的有效措施研究

采用循环注CO2吞吐方法直接处理低产油井,要比用注水井对采油井的间接处理还要经济得多,而且驱油效率也较高。只要措施得当、注采制度合理,具有投资少、偿还快的特点,其风险远比其他强化采油法要小得多。有必要总结近年来已实施的二氧化碳吞吐的效果及其影响因素,在此基础上开展二氧化碳吞吐技术政策研究,形成图版,指导下步CO2吞吐井的筛选与优化设计,提升五号桩油田二氧化碳吞吐效果。

推荐一种新硝化剂五氧化二氮及其工业化的生产方法

硝化是化学工业广泛应用的反应，但常规硝化剂是由浓硝酸和浓硫酸混成的，它是一种非常落后且危险性很大的硝化剂。五氧化二氮（N_2O_5）硝化剂比常规混合酸硝化剂有五大优点，因为它可用半渗透膜电解池法制造，所以今天五氧化二氮商品可以由工业化装置生产。建议国内各浓硝酸生产厂结合各自工艺特长创造性发展新硝化剂生产。

油菜花粉诱导合成多孔中空催化剂Nb_2O_5/TiO_2及其在醇氧化反应中的应用

采用油菜花粉为模板制备了一种具有多孔中空结构的催化剂——五氧化二铌/二氧化钛(Nb2O5/Ti O2),它在光照下的醇氧化反应中表现出良好的活性。反应可以在无溶剂下进行,以O2作为氧化剂,2,2,6,6-四甲基哌啶-N-氧自由基(TEMPO)作为助催化剂,反应过程绿色环保,对环境友好。该体系下,10 m L苯甲醇可以得到31mmol苯甲醛,收率为33%,选择性达98%。与单纯用Ti O2作催化剂相比,该文所制催化剂具有多孔结构及Nb2O5,反应的选择性提高。

Reduction and deposition of arsenic in copper electrolyte

The influences of temperature, H2SO4 concentration, CuSO4 concentration, reaction time and SO2 flow rate on the reduction of arsenic（V） with SO2 were studied and the deposition behavior of arsenic （III） under the effect of concentration and co-crystallization was investigated in copper electrolyte. The results indicate that reduction rate of arsenic （V） decreases with increasing temperature and H2SO4 concentration, but increases with increasing SO2 flow rate and reaction time, and it can reach 92% under appropriate conditions that reaction temperature is 65 °C, H2SO4 concentration is 203 g/L, CuSO4 concentration is 80 g/L, reaction time is 2 h and SO2 gas flow rate is 200 mL/min. To remove arsenic in the copper electrolyte, arsenic （V） is reduced to trivalence under the appropriate conditions, the copper electrolyte is concentrated till H2SO4 concentration reaches 645 g/L, and then the removal rates of As, Cu, Sb and Bi reach 83.9%, 87.1%, 21.0% and 84.7%. The XRD analysis shows that crystallized product obtained contains As2O3 and CuSO4·5H2O.

Characterization of V_2O_5/MoO_3 composite photocatalysts prepared via electrospinning and their photodegradation activity for dimethyl phthalate

Vanadium pentoxide（V2O5）/molybdenum trioxide（MoO 3） composites with different molar ratios of vanadium（V） to molybdenum（Mo） were synthesized via a simple electrospinning technique. The photocatalytic activity of the composites were evaluated by their ability to photodegrade methylene blue and dimethyl phthalate（DMP） under visible-light irradiation. Compared with pure V2O5 and MoO 3,the V2O5/MoO 3 composites showed enhanced visible-light photocatalytic activity because of a V 3d impurity energy level and the formation of heterostructures at the interface between V2O5 and MoO 3. The optimal molar ratio of V to Mo in the V2O5/MoO 3 composites was found to be around 1/2. Furthermore,high-performance liquid chromatographic monitoring revealed that phthalic acid was the main intermediate in the photocatalytic degradation process of DMP.

Elimination of 1,2-dichloroethane over(Ce,Cr)_x O_2/Nb_2O_5 catalysts: synergistic performance between oxidizing ability and acidity

A series of(Ce,Cr)xO2/Nb2O5 catalysts with different(Ce,Cr)xO2 to Nb2O5 mass ratios were synthesized by the deposition-precipitation method for use in deep catalytic oxidation of 1,2-dichloroethane(DCE), which is one of the typical chlorinated volatile organic compound pollutants. The textural properties were characterized by X-ray diffraction, N2 adsorption/desorption isotherms, UV-Raman spectroscopy, and scanning electron microscopy. The surface acidity and the redox properties were characterized by ammonia temperature-programmed desorption and H2 temperature-programmed reduction, respectively. The results show that the addition of a proper amount of(Ce,Cr)xO2 over Nb2O5 significantly improves the intrinsic catalytic activity towards the deep oxidation of DCE, and only a very small amount of C2H3Cl is detected as the byproduct of the oxidation process. Further study reveals the existence of an obvious synergistic effect between Nb2O5, with abundant strong acid sites, and(Ce,Cr)xO2, with strong oxidation sites, as the strong acid sites of Nb2O5 promote the adsorption and dehydrochlorination of DCE, while the strong oxidation sites of(Ce,Cr)xO2 contribute to the deep oxidation of the reactant, intermediates, and byproducts.

Solvothermal Synthesis of V_2O_3 Catalysts for Oxidative Desulfurization of Dibenzothiophene

V2O3 nanoparticles with high surface area have been successfully prepared by a new solvothermal method without using any surfactant and template. The size of V2O3 nanoparticles is mostly equal to 10 nm-30 nm. The highest surface area of obtained V2O3 nanoparticles reaches 49 m2/g. Several kinds of V2O3 catalysts were prepared by different methods. All these V2O3 catalysts obtained thereby showed high catalytic activity for oxidative desulfurization(ODS) reaction by using tert-butyl hydroperoxide as the oxidant. The V2O3 catalyst with a highest ODS activity was obtained under the following conditions: The catalyst was prepared upon using V2O5 as the vanadium source, methanol as the solvent, and oxalic acid as the complexing reagent at a V2O5/oxalic acid molar ratio of 1:2. The process for ODS of dibenzothiophene was carried out under mild conditions(under atmospheric pressure and at a relatively low temperature). The highest ODS activity of the obtained V2O3 nanoparticles can be attributed to their highest surface area.

Hydrothermal Synthesis and Crystal Structure of [H_4As_8V_(14)O_(42)(H_2O)]·6H_2O

The title compound [H4As8V14O42(H2O)]6H2O 1 has been synthesized and characterized by elemental analysis, IR, and single-crystal X-ray diffraction analysis. It crystallizes in trigonal, space group R3c with a = b = 36.447(6), c = 21.485(5) ? V = 24717(8) 3, Z = 18, Mr = 2114.66, Dc = 2.557g/cm3, F(000) = 17928, m = 7.149 mm-1, R = 0.0792 and wR = 0.1265. The [H4As8V14O42- (H2O)] cluster consists of fourteen VO5 square pyramids linked by four As2O5 handle-like units.

Preparation of TiO_2 photocatalyst loaded with V_2O_5 for O_2 evolution

TiO2 photocatalysts loaded with V2O5 were prepared via a modified hydrolysis process,and characterized by X-ray diffraction,transmission electron microscopy,Raman spectra and diffuse reflectance UV-Vis spectra measurements. The photocatalytic activity of V2O5/TiO2 was investigated by employing splitting of water for O2 evolution. The results indicate that V2O5 loading can pronouncedly improve the photocatalytic activity of TiO2 with Fe3+ as an electron acceptor under UV or visible light irradiation. The optimum mass fraction of the loaded V2O5 is 8%,and the largest speed of O2 evolution for 8%V2O5 (mass fraction) loaded TiO2 catalyst is 118.2 μmol/(L.h) under UV irradiation,and 83.7 μmol/(L.h) under visible light irradiation.

“Water in salt/ionic liquid”electrolyte for 2.8 V aqueous lithium-ion capacitor

Development of high-voltage electrolytes with non-flammability is significantly important for future energy storage devices.Aqueous electrolytes are inherently non-flammable,easy to handle,and their electrochemical stability windows(ESWs)can be considerably expanded by increasing electrolyte concentrations.However,further breakthroughs of their ESWs encounter bottlenecks because of the limited salt solubility,leading to that most of the high-energy anode materials can hardly function reversibly in aqueous electrolytes.Here,by introducing a non-flammable ionic liquid as co-solvent in a lithium salt/water system,we develop a"water in salt/ionic liquid"(WiSIL)electrolyte with extremely low water content.In such WiSIL electrolyte,commercial niobium pentoxide(Nb2O5)material can operate at a low potential(-1.6 V versus Ag/AgCl)and contribute its full capacity.Consequently,the resultant Nb2O5-based aqueous lithium-ion capacitor is able to operate at a high voltage of 2.8 V along with long cycling stability over 3000 cycles,and displays comparable energy and power performance(51.9 Wh kg^-1 at 0.37 kW kg^-1 and 16.4 Wh kg^-1 at 4.9 kW kg^-1)to those using non-aqueous electrolytes but with improved safety performance and manufacturing efficiency.