pH值及助剂对氢化态Mg-Mn复合物水反应性能的影响

为了提高氢化态Mg-Mn复合物的水反应性能,采用改变反应水溶液pH值和在水溶液中加入不同助剂的方法,通过测量反应过程中不同时刻产生的氢气量对助剂在水反应中的作用进行表征,利用SEM和XRD等测试手段对反应产物进行表征和测试,对反应机理进行分析。结果表明:改变反应溶液的pH值对反应程度及放氢速率的影响不大,且pH值越大,越不利于反应的进行;在溶液中添加助剂焦磷酸钾、六偏磷酸钠、羟基乙叉二膦酸(HEDP)对提高氢化态Mg-Mn复合物的放氢速率有显著促进作用;相比之下,应采用添加磷酸盐助剂的方法来改善氢化态Mg-Mn复合物水反应性能。

不同种类离子对Al-Mg-Li-Zr合金粉末水反应性能的影响

使用高压反应釜对Al-Mg-Li-Zr合金粉末的水反应性能进行了研究,通过对反应体系的温度–时间(T-t)曲线进行分析,提取出了反应启动温度、反应时间、放热温升与平均升温速率四个特征参数,重点研究了不同种类离子对Al-Mg-Li-Zr合金粉末水反应性能的影响。结果表明,相较于蒸馏水,大部分盐溶液均使得Al-Mg-Li-Zr合金粉末的水反应启动温度降低。硝酸根、硫酸根、氯离子、钾离子与钠离子均对Al-Mg-Li-Zr合金粉末的水反应起到促进作用,其中,KNO3的促进效果最好,而氟化盐则明显抑制了Al-Mg-Li-Zr合金粉末的水反应。

Supercritical-hydrothermal accelerated solid state reaction route for synthesis of LiMn_2O_4 cathode material for high-power Li-ion batteries

Synthesis of the spinel structure lithium manganese oxide （LiMn2O4） by supercritical hydrothermal （SH） accelerated solid state reaction （SSR） route was studied. The impacts of the reaction pressure, reaction temperature and reaction time of SH route, and the calcination temperature of SSR route on the purity, particle morphology and electrochemical properties of the prepared LiMn2O4 materials were studied. The experimental results show that after 15 min reaction in SH route at 400 ℃ and 30 MPa, the reaction time of SSR could be significantly decreased, e.g. down to 3 h with the formation temperature of 800 ℃, compared with the conventional solid state reaction method. The prepared LiMn2O4 material exhibits good crystallinity, uniform size distribution and good electrochemical performance, and has an initial specific capacity of 120 mA.h/g at a rate of 0.1C （1C=148 mA/g） and a good rate capability at high rates, even up to 50C.

Design of best performing hexagonal shaped Ag@CoS/rGO nanocomposite electrode material for electrochemical supercapacitor application

The mixed metal/metal sulphide(Ag@CoS)with reduced graphene oxide(rGO)nanocomposite(Ag@CoS/rGO)was synthesized for the possible electrode in supercapacitors.Ag@CoS was successfully deposited on the rGO nanosheets by hydrothermal method,implying the growth of 2D Ag and CoS-based hexagonal-like structure on the rGO framework.The synthesized nanocomposite was subjected to structural,morphological and electrochemical studies.The XRD results show that the prepared nanocomposite material exhibits a combination of hexagonal and cubic phase due to the presence of CoS and Ag phases together.The band appearing at nearly 470.33 cm^−1 in FTIR spectra can be ascribed to the absorption of S—S bond in the Ag@CoS/rGO nanocomposite.The clear hexagonal structure was analysed by SEM and TEM with the grain sizes ranging from nanometer to micrometer.The electrode material exhibits excellent cyclic stability with a specific capacitance of 1580 F/g at a current density of 0.5 A/g without any loss of capacitive retention even after 1000 cycles.Based on the electrochemical performance,it can be inferred that the prepared novel nanocomposite material is very suitable for using as an electrode for electrochemical supercapacitor applications.

Toluene degradation by a water/silicone oil mixture for the design of two phase partitioning bioreactors

Toluene degradation performances were studied in a 10 L Two-Phase Partitioning Bioreactor(TPPB).The liquid phase consisted of a mixture of water and PDMS 50(Poly Di Methyl Siloxane,i.e.silicone oil,viscosity of 46 m Pa·s) in the volume ratio of 75%/25%.Two series of experiments were carried out:in the first,the reactor was sequentially supplied with toluene whereas in the second,toluene was continuously supplied.Activated sludge from the wastewater treatment plant of Beaurade(Rennes,France) was used at an initial concentration of 0.5 dry mass g·(mixture L)^(-1).The elimination capacity(EC) was investigated as well as the change in biomass concentration over time.Toluene biodegradation was very ef ficient(removal ef ficiency,RE=100%) for toluene flows ranging from 0.2 to 1.2 ml·h^(-1),corresponding to elimination capacities of up to 104 g·m^(-3)·h^(-1).For a toluene flow of 1.2 ml·h^(-1),the biomass concentration measured at the end of the experiment was 4.7 dry mass g·(mixture L)^(-1).The oxygen concentration in the liquid phase was clearly not a limiting factor in these operating conditions.Based on these results,an extrapolation leading to the design of a large-scale pilot TPPB can now be considered to study toluene degradation performances in industrial conditions.

The Effect of Non-acidified Wastewater on Expanded Granular Sludge Bed （EGSB） Reactors Performance

The textile processing plants utilize a wide variety of dyes and other chemicals such as acids, bases, salts, detergents, sizes, oxidants, mercerizing and finishing chemicals. Many of these are not retained in the final product and are discharged in the effluent. Therefore, the objective of this study was to assess the performance of EGSB （Expanded Granular Sludge Bed） reactor to treat non-acidifie wastewater. Several experiments using starch and volatile fatty acids as model substrates were conducted. The problems of piston formation were evaluated at a variety of relevant operational conditions, such as substrate concentration, organic and hydraulic loading rates. The results showed that newly grown acidogenic biomass diluted original methanogenic biomass and the granular sludge in the EGSB reactor deteriorated. The piston formation in the EGSB reactor that was fed with non-acidified wastewater occurred due to high growth of acidogenic biomass and high upflow velocity applied in the system.

Molecular-Based Simulation of Feedstock Properties for Complex Reaction System

The kinetics of complex reaction systems were studied on molecular level with the combined method of Monte Carlo simulation and Structural Oriented Lumping by focusing on deep catalytic cracking （DCC） process, the model parameters were optimized by means of routine analytic data of a DCC unit. A model was established to transform the feedstock of the complex reaction systems such as DCC to 1000-10000 pseudo-molecules with the Monte Carlo simulation and every molecule was expressed by 19 attributes. The results of model simulation showed that these pseudo-molecules reflected the characteristics of feedstock very well and their average properties gave a good agreement with the plant data.

Revisiting Stainless Steel as PWR Fuel Rod Cladding after Fukushima Daiichi Accident

In the past, stainless steel was utilized as cladding in many PWRs （pressurized water reactors）, and its performance under irradiation was excellent. However, stainless steel was replaced by zirconium-based alloy as cladding material mainly due to its lower neutron absorption cross section. Now, stainless steel cladding appears as a possible solution for safety problems related to hydrogen production and explosion as occurred in Fukushima Daiichi accident. The aim of this paper is to discuss the steady-state irradiation performance using stainless steel as cladding. The results show that stainless steel rods display higher fuel temperatures and wider pellet-cladding gaps than Zircaloy rods and no gap closure. The thermal performance of the two rods is very similar and the neutron absorption penalty due to stainless steel use could be compensating by combining small increase in U-235 enrichment and pitch size changes.

LOFT L9-3 Experiment Simulation Using the SPACE Code

The KHNP （Korea Hydro ＆ Nuclear Power Co.） has developed a multipurpose nuclear safety analysis code called SPACE （the safety and performance analysis code） for nuclear power plants. SPACE code is a best-estimated two-phase three-field thermal-hydraulic analysis code used to analyze the safety and performance of pressurized water reactors. In this paper, LOFT （loss of fluid test） L9-3 experiment using the SPACE code was selected to confirm the capability of SPACE code and the results calculated by the SPACE code are compared with those measured through the experiment. The results were compared with the experimental data and those of the other code simulations. Throughout the simulation result, it was concluded that the SPACE code can effectively simulate LOFT L9-3 experiment.

Performance Comparison of Two Newly Developed Bimetallic(X-Mo/Al2O3, X=Fe or Co) Catalysts for Reverse Water Gas Shift Reaction

The performance of the two newly developed bimetallic catalysts based on the precursor, Mo/Al_2O_3, was compared for reverse water gas shift(RWGS) reaction. The structures of the precursor and the catalysts were studied using X-ray diffraction(XRD), Brunauer–Emmett–Teller(BET) analysis, inductively coupled plasma-atomic emission spectrometry(ICP-AES), CO chemisorption, temperature programmed reduction of hydrogen(H_2-TPR) and scanning electron microscopy(SEM) techniques. The activity of Fe-Mo and Co-Mo catalysts was compared in a fixed bed reactor at different temperatures. It is shown that the Co-Mo catalyst has higher CO_2 conversion at all temperature level. The time-on-stream(TOS) analysis of the activity of catalysts for the RWGS reaction was carried out over a continuous period of 60h for both catalysts. The Fe-Mo/Al_2O_3 catalyst exhibits good stability within a period of 60h, however, the Co-Mo/Al_2O_3 is gradually deactivated after 50h of reaction time. Existence of(Fe_2(MoO4_))_3 phase in Fe-Mo/Al_2O_3 catalyst makes this catalyst more stable for RWGS reaction.

Performance of simultaneous desulfurization and denitration in liquid phase with new-style complex absorbent

Performance of simultaneous desulfurization and denitration using the solution of NaClO2 and NaClO as new-style complex absorbent was investigated experimentally in self-designed bench scale bubbling reactor. The effects of main parameters, such as the concentrations of NaClO2 and of NaClO, solution pH and reaction temperature and so on, on removal efficiencies of SO2 and NOx, were examined, then the optimal conditions were established, in which the molar ratio of NaClO to NaClO2 was 1：1, the reaction temperature was 50℃ and the solution pH was 5.5. The removal efficiencies of SO2 and NO under the optimal conditions were 100% and 89.2%, respectively. The mechanism of simultaneous removal based on complex absorbent was proposed by analyzing the removal products and the electrode potentials of related species, namely SO2 and NO are oxi- dized by chlorite anion, hypochlorite, chlorine dioxide and chlorine contained in complex absorbent. In thermodynamic aspect, simultaneous desulfurization and denitration reactions in liquid phase can happen spontaneously and completely, and are all exothermic reactions. It was confirmed by kinetics that for simultaneous desulfurization and denitration, the reaction order and average activation energy of SO2 were 1 and 21.6 kJ·mol^-1, respectively, and those of NO were 1 and 8.2 kJ·mol^-1, respectively.

Application of nanoindentation to investigate chemomechanical properties change of cement paste in the carbonation reaction

Nanoindentation technique was adopted to investigate the chemomechanical properties change of hardened cement paste before and after carbonation.It was found that the mean elastic modulus and mean hardness obviously increase after the carbonation reaction.Specifically,the probability of the elastic modulus showed a sharp reduction for the elastic modulus at the range of 7-34 and 83-160 GPa,in comparison of a large increase for the elastic modulus between 34-83 GPa.For the same reason,the probability of the hardness showed a large decrease when the hardness fell within 0.15-1.75 and 4.15-8.20 GPa and a dramatic increase for the hardness at the range of 1.75-4.15 GPa.In addition,low density C-S-H was affected by the carbonation degradation more seriously than high density C-S-H.The carbonation reaction led to distinct decrease of the number and size of unhydrated cement paste particles.

S, N co-doped carbon nanotube-encapsulated core-shelled CoS2@Co nanoparticles： efficient and stable bifunctional catalysts for overall water splitting

Hydrogen, serving as a clean, sustainable energy source, may be mainly produced from electrolysis water. Herein, we report cobalt disulphide encapsulated in self-catalyzed carbon nanotubes （S, N-CNTs/ CoS2@Co） serving as a bifunctional catalyst, which exhibits excellent hydrogen evolution reaction perfor-mance （10.0 mAcm^-2 at 0.112 V, and low Tafel slope for 104.9 mV dec^-1 ） and oxygen evolution reaction performance （10.0 mAcm^-2 at 1.57 V, and low Tafel slope for 76.1 mV dec^-1）, meanwbile with a strong stability at various current densities. In-depth study reveals that the excellent catalytic properties can be mainly attributed to the increased catalytic sites induced by S, N co-doping, the improved electronic con-ductivity derived from the carbon nanotubes, and Mott-Schottky effect between the metal cobalt and semiconductive cobalt disulfide. Notably, when the bifunctional catalysts are applied to overall water splitting, a low potential of 1.633 V at the current density of 10.0 mAcm^-2 is achieved, which can com-pete with the precious metal catalyst benchmarks in alkaline media, demonstrating its promising prac-ticability in the realistic water splitting application. This work elucidates a practicable way to the design of transition metal and nano-carbon composite catalysts for a broad application in the fields of energy chemistry.