各类有机物的氧化反应

本文简要叙述了有机反应中常见的氧化剂、氧化剂溶液的配制以及各类有机物氧化反应的情况.

污水处理厂除臭装置设计实例

本文介绍城市污水处理厂致臭气体的化学吸收装置设计实例。采用硫酸溶液和碱性氧化剂溶液作吸收介质,恶 臭气体氨气、硫化氢、甲硫醇通过三级吸收塔被吸收,气体达标后排放。

澳瑞凯乳胶基质生产线在准能公司炸药厂的应用

介绍了乳胶基质生产线在神华准能公司炸药厂的应用,乳胶基质制备设备的使用情况及特点,创造的经济效益和一些建议。

Co-intensification of cyanide leaching gold by mercury ions and oxidant

The effects of mercury ions on gold cyanidation were studied. The results show that under low cyanide concentration, gold cyanide process is controlled by CN- transfer, while at higher cyanide concentration, there forms passivation on gold surface. Therefore, chemical oxidation of gold in cyanide solution of higher concentration is controlled by surface reaction. Small quantity of additions of mercury ions bring about great increases in anodic gold dissolution rate, decreases the passivation and reduces the equilibrium activated energy. In addition, they also markedly change the effect pattern of cyanide concentration. Mercury ions show positive effects on cathodic reduction of oxygen and raise the rate of electrochemical step of the cathodic reduction of oxygen. Addition of a certain amount of hydrogen peroxide is confirmed to be an effective way for intensification of cathodic process on gold electrode. Active potential range and current peak on anodic dissolution are enlarged when being co-intensified with Hg^2＋ and hydrogen peroxide. Co-intensifying effect may be obtained and gold from gold concentrates. gold leaching rate is considerably increased on cyanide leaching of

Wettability and surfactivity of sodium phosphate surfactants in strong alkali solutions

The wettability,surfactivity and the correlation between wettability and surfactivity of sodium diethylhexylphosphate,sodium diethylhexyl polyoxyethylene phosphate and their complex in NaOH solutions were studied.A complex alkali resistant phosphate surfactant with good permeability was prepared.The wettability of surfactants was investigated by measuring the immersion time,sinking time and capillary effects of nature cotton grey fabric in NaOH solutions.The surfactivity of the surfactants was characterized by measuring the surface tension.The effect of the complex on the surface appearance of cotton grey fabric was also investigated with a scanning electron microscope(SEM) .The results show that all the surfactants exhibit good wettability for cotton grey fabric in 0.5-5.0 mol/L of NaOH solutions,the complex system exhibits better wettability in 5.0-7.0 mol/L of NaOH solutions,in comparison with either corresponding single surfactant component employed,and wettability is well correlative with the surfactivities of the surfactant.SEM images indicate that the cotton grey fabric is well wetted by the alkaline surfactant solution and the quality of fabric is improved.

Study of the Liquid Phase Volume Expansion for CO_2/Organic Solvent Systems

The supercritical antisolvent （SAS） process has been developed in recent years for the tormation of nanoand micro-particles. It is necessary to study the liquid phase volume expansion （LPVE） and find the relationships between the operating conditions and the LPVE in order to develop a practical method for determining the operation conditions and selecting an organic solvent for SAS process. The PR equation of state with vdW-1 mixing rule is used to calculate the LPVE for CO2/toluene, CO2/acetone and CO2/ethyl acetate systems, and the results show that the LPVE for each CO2/organic solvent system decreases as the temperature increases. The relationship between the LPVE and the solubility of CO2 in the liquid phase for CO2/organic solvent systems is investigated, and the results show that the LPVE is determined directly by the solubility of CO2 in the liquid phase, xCO2, and can be related to xCO2 independently. No matter what system of CO2/organic solvent is and how different the temperature is, the LPVEs have little difference as long as the solubility of CO2 in the liquid phase, xCO2, keeps constant. The lower temperature is always favorable to the SAS process. The higher the solubility of CO2 in an organic solvent under certain operation condition, the more suitable it is to the SAS process.

Precipitation of antimony from the solution of sodium thioantimonite by air oxidation in the presence of catalytic agents

The behavior of antimony oxidation in the solution of sodium thioantimonite was studied in the presence of catalytic agents. The catalytic effects of the respective addition of cupric sulfate, sodium tartrate, potassium permanganate, phenol, 1,2 dihydroxybenzene and their combination on the oxidation of sodium thioantimonite were investigated. A pilot test was carried out. The results show that the respective use of sodium tartrate, cupric sulfate, potassium permanganate, phenol and 1,2 dihydroxybenzene have little catalytic effect on the oxidation of sodium thioantimonite. However there exists obvious catalytic oxidation by the combination of 0.25 g/L 1,2 dihydroxybenzene, 0.5 g/L potassium permanganate and 1.0 g/L phenol. Moreover, high blast intensity, the increase of temperature and NaOH concentration favor the oxidation of antimony. The oxidation process of antimony has such advantages as quick reaction and low operation costs. The results of the pilot test are consistent with those of laboratory experiments.

Leaching kinetics of molybdenum from Ni-Mo ore in sulfuric acid solution with sodium peroxodisulfate as oxidant

The leaching kinetics of molybdenum from Ni-Mo ore in sulfuric acid solution with sodium peroxodisulfate was studied.The effects including leaching temperature, reaction time, particle size, stirring speed, and concentrations of sulfuric acid and sodium peroxodisulfate were investigated. The leaching process of molybdenum from Ni-Mo ore is controlled by the chemical reaction through the solid layer across the unreacted shrinking core. The apparent activation energy of the leaching of molybdenum is calculated to be 41.0 k J/mol and the leaching kinetics equation of molybdenum from Ni-Mo ore is expressed as1-(1-a)1/3=3405.7exp[-41030.0/(RT)]t.

Selection of Chelated Fe(Ⅲ)/Fe(Ⅱ) Catalytic Oxidation Agents for Desulfurization Based on Iron Complexation Method

Optimization of factors influencing the experiments on reactions involving 8 different chelating agents and soluble Fe(III)/Fe(II) salts was carried out to yield chelated iron complexes. A combination of optimized influencing factors has resulted in a Fe chelating capacity of the iron-based desulfurization solution to be equal to 6.83—13.56 g/L at a redox potential of 0.185—0.3. The desulfurization performance of Fe(III)/Fe(II) chelating agents was investigated on a simulated sulfur-containing industrial gas composed of H2 S and N2 in a cross-flow rotating packed bed. Test results have revealed that the proposed iron-based desulfurization solution showed a sulfur removal efficiency of over 99% along with a Fe chelating capacity exceeding 1.35 g/L. This desulfurization technology which has practical application prospect is currently in the phase of commercial scale-up study.

Heterogeneous Advanced Photo-Fenton Oxidation of Phenolic Aqueous Solutions over Iron-Containing SBA-15 Catalyst

Iron-containing SBA-15 catalysts have been prepared following different synthesis routes, direct synthesis by adjusting pH at 3 and 6 and with post synthesis procedure. Activity and stability of these materials were assessed on the photo-Fenton degradation of phenolic aqueous solutions by H2O2 using near ultraviolet irradiation （254 nm） at room temperature and initial neutral pH. Their catalytic performance was mentioned in terms of phenol and TOC （total organic carbon） conversions. Several complementary techniques, including X-ray, nitrogen sorption isotherms, UV （Ultraviolet） visible, were used to evaluate the final structural and textural properties of calcined Fe-SBA 15 materials. These materials show a high activity and stability of iron species.

Photocatalytic activity of CuO towards HER in catalyst from oxalic acid solution under simulated sunlight irradiation

CuO was synthesized by thermal decomposition of Cu(NO3)2·3H2O at various temperatures and characterized by powder X-ray diffractometry(XRD) as well as scanning electron microscopy(SEM).The effects of calcination temperature,category of sacrificial reagent,initial sacrificial reagent concentration,and Ag loading content on the photocatalytic activity of the as-obtained CuO sample were investigated.The results show that the as-obtained CuO exhibits high activity for photocatalysis of H2 evolution reaction(HER) in oxalic acid solution under simulated sunlight irradiation.The highest photocatalytic activity of the as-obtained CuO was achieved at the calcination temperature of 1000℃,and oxalic acid was used as the sacrificial reagent with the concentration 0.05 mol/L.H2 evolution rate is as high as 2.98 mmol/(h·g) with 2%(mass fraction) loaded Ag.The possible photocatalytic reaction mechanism on the CuO photocatalyst for HER in oxalic acid solution was also discussed.

Removal of mercaptans from light oils using ionic liquid–NaOH aqueous solution as extractants

The application of ionic liquids as alternatives to conventional organic solvents in the extraction process has been investigated. In the present study, fourteen species of imidazolium-based ionic liquids were added into the NaOH （aq） to remove the mercaptans. The influences of anion species and cation alkyl chain length of the imidazolium-based ionic liquids on the performance of mercaptan removal from light oils have been discussed. The efficiency of extraction for mercaptans exhibited the order of [Ac]- 〉 [OH]- [Br]- 〉 [BF4]-. The longer alkyl chain imidazolium-based ionic liquids contributed to enhance desulfurization rate of l-butyl mercaptan. 100% desulfurization rate of l-butyl mercaptan was achieved by the anion of Ac- ionic liquids and NaOH （aq） at a volume ratio of 40：1 （V（oil]：Vfionic liouid）） and a short eouilibrium time within 10 min.

Process simulation and analysis of carbon capture with an aqueous mixture of ionic liquid and monoethanolamine solvent

This study investigated the prospect of using aqueous mixture of 1-butylpyridinium tetrafluoroborate （[Bpy][BF4]） ionic liquid （IL） and monoethanolamine （MEA） as solvent in post-combustion CO2 capture （PCC） process. This is done by analysis of the process through modelling and simulation. In literature, reported PCC models with a mixture of IL and MEA solvent were developed using equilibrium-based mass transfer approach. In contrast, the model in this study is developed using rate-based mass transfer approach in Aspen Plus. From the results, the mixed aqueous solvent with 5-30 wt% IL and 30 wt% MEA showed 7%-9% and 12%-27% less specific regeneration energy and solvent circulation rate respectively compared to commonly used 30 wt% MEA solvent. It is concluded that the ｜L concentration （wt%） in the solvent blend have significant impact on specific regeneration energy and solvent circulation rate. This study is a starting point for further research on technical and economic analysis of PCC process with aqueous blend of IL and MEA as solvent.

Active catalysts based on cobalt oxide@cobalt/N-C nanocomposites for oxygen reduction reaction in alkaline solutions

Over the past few years, electrocatalysis for the oxygen reduction reaction in alkaline solutions has undergone tremendous advances, and non-precious metal catalysts are of prime interest. In this study, we present a highly promising CoO@Co/N-C （where N-C represents a N-doped carbon material） catalyst, achieving an onset potential of 0.99 V （versus the reversible hydrogen electrode （RHE）） and a limiting current density of 7.07 mA-cm-2 （at 0.3 V versus RHE） at a rotation rate of 2,500 rpm in an O2-saturated 0.1 M KOH solution, comparable to a commercial Pt/C catalyst. The H2--O2 alkaline fuel cell test of CoO@Co/N-C as the cathode reveals a maximum power density of 237 mW.cm 2. Detailed investigation clarifies that a synergistic effect, induced by C-N, Co-N-C, and CoO/Co moieties, is responsible for the bulk of the gain in catalytic activity.

Adsorption of As(Ⅲ)from aqueous solution based on porous magnetic/chitosan/ferric hydroxide microspheres prepared via electrospraying

Porous chitosan（CS）/magnetic（Fe304）/ferric hydroxide（Fe（OH）3） microsphere as novel and low-cost adsorbents for the removal of As（Ill） have been synthesized via the electrospraying technology by a simple process of two steps. Characterization of the obtained adsorbents was studied by transmission electron microscopy （TEM）, scanning electron microscopy （SEM）, X-ray photoelectron spectroscopy （XPS）, and X-ray diffraction （XRD）. The adsorption kinetics and equilibrium isotherms were in- vestigated in batch experiments. The Langmuir, Freundlich isotherm and pseudo-second order kinetic models agree well with the experimental data. The adsorption of As（III） onto CS/Fe3OdFe（OH）3 microspheres occurred rapidly and reached adsorption equilibrium after about 45 min. The maximum adsorption capacity of CS/Fe3OJFe（OH）3 microspheres, calculated by the Langmuir isotherm model, was 8.47 mg g 1, which is higher than that of CS/Fe304/Fe（OH）3 prepared by the conventional method （4.72 mg g-l）. The results showed that the microspheres had a high adsorption capacity for As（III） and a high separation efficiency due to their microporous structure and superparamagnetic characteristics. Present research may eventually lead to a simple and low cost method for fabricating microporous materials and application for removal of arsenic from aqueous solution.

Pyridine-modulated Ni/Co bimetallic metal-organic framework nanoplates for electrocatalytic oxygen evolution

Two-dimensional(2D)metal-organic frameworks(MOFs)are promising for electrocatalysis with high performance,as they possess large surface areas and high densities of exposed active sites.It attracts tremendous attention to obtain 2D nanostructures via simple preparation methods.Herein,a facile pyridine-modulated solvothermal synthesis of Ni/Co bimetallic MOF nanoplates(NixCoy-bpy(PyM))is reported with well-defined 2D morphology with a thickness as thin as 20 nm and an aspect ratio larger than 50.These nanoplates possess oxygen evolution reaction activity as electrocatalysts in alkaline conditions.Specifically,Ni0.5Co1.5-bpy(PyM)exhibits excellent OER electrocatalytic activity with a low overpotential of 256 mV at 10 m A cm-2 and a small Tafel slope of 81.8 mV dec-1 in 1.0 mol L-1 KOH with long-term electrochemical stability for 3000 cyclic voltammetry cycles.The high catalytic activity of Ni0.5Co1.5-bpy(PyM)can be attributed to the in situ formed active hydroxide and oxyhydroxide species within the inherited 2D morphology and the optimized bimetallic ratio.

Ozonated graphene oxides as high efficient sorbents for Sr(Ⅱ) and U(Ⅵ) removal from aqueous solutions

Ozone was used to oxidize graphene oxides （GO） to generate ozonated graphene oxides （OGO） with higher oxygen-containing functional groups. The as-prepared OGO was characterized by Fourier transformed infrared spectroscopy （FTIR）, scanning electron microscopy （SEM） and X-ray photoelectron spectroscopy （XPS）. Based on the results of potentiometric acid-base ti- trations, the total carboxylic acid concentration on OGO surface was calculated to be 3.92 retool/g, which was much higher than that on GO surface. The results of adsorption experiments indicated that the adsorption capacities of OGO for Sr（II） and U（VI） removal were improved significantly after ozonization.