In situ chemical oxidation of aniline by persulfate with iron(Ⅱ) activation at ambient temperature

The kinetics of aniline degradation by persulfate processes with iron（Ⅱ） activation at ambient temperature was investigated in this study.With iron（Ⅱ） as initiator,the oxidation reactions were found to follow a biphasic rate phenomenon：a rapid transformation followed by a slow but sustained oxidation process.In the first 30 s,the reaction mainly relies on the persulfate-Fe^（2＋） reaction in which aniline is oxidized rapidly.After 30 s,the aniline was still oxidized but the rate of reaction tended to be slower and the rates were clearly linear-proportional.After the initial fast oxidation,the reactions appeared to follow a pseudo-first-order model.

Preparation of Anode Material for Lithium Ion Battery by Chemical Oxidation

Anode material for lithium ion battery is prepared by chemical oxidation of natural graphite. After oxidation, the properties of natural graphite are modified, such as surface structure, the content of graphite phases, the number of micropores and its stability. thus the modified natural graphite can be used as anode material for commercial lithium ion battery. The reversible capacity is increased from 100 mAh/g to above 300 mAh/g, and its cycling properly is also satisfactory.

Study on treatment of acidic black 10B dye wastewater by chemical oxidation and adsorption of activated carbon fixed bed

Acidic black 10B dye wastewater was treated by chemical oxidation and adsorption of activated carbon fixed bed and all kinds of influential factors of removal CODcr were discussed. When the initial concentration of the dye was 150 mg/L, CODer was 432 mg/L and chrome was 2800 times, the appropriate conditions determined by the experiment were as follows： r（NaC10）--4.84 g/L, 25 min, pH=6, height of activated carbon fixed bed was 10 cm. Under these conditions, the decolorizing rate can come up to about 100% and total removed rate of CODer reached at 89.6%. Comparison of UV-Vis adsorption spectrums before and after treatment showed that decomposition effects of chemical oxidation and adsorption of activated carbon fixed bed on acidic black 10B dye wastewater were satisfactory.

The performance and mechanism of iron-mediated chemical oxidation:Advances in hydrogen peroxide,persulfate and percarbonate oxidation

Many studies have successfully built iron-mediatedmaterials to activate or catalyze Fentonlike reactions,with applications in water and wastewater treatment being investigated.However,the developed materials are rarely compared with each other regarding their performance of organic contaminant removal.In this review,the recent advances of Fentonlike processes in homogeneous and heterogeneous ways are summarized,especially the performance and mechanism of activators including ferrous iron,zero valent iron,iron oxides,iron-loaded carbon,zeolite,and metal organic framework materials.Also,this work mainly compares three O-O bond containing oxidants including hydrogen dioxide,persulfate,and percarbonate,which are environmental-friendly oxidants and feasible for in-situ chemical oxidation.The influence of reaction conditions,catalyst properties and benefits are analyzed and compared.In addition,the challenges and strategies of these oxidants in applications and the major mechanisms of the oxidation process have been discussed.This work can help understand the mechanistic insights of variable Fenton-like reactions,the role of emerging iron-based materials,and provide guidance for choosing appropriate technologies when facing real-world water and wastewater applications.

Ethane Chemical Looping Oxidative Dehydrogenation to Ethylene over Co_(2)O_(3)(Fe_(2)O_(3),NiO)/LaCoO_(3) Oxygen Carriers

Ethane chemical looping oxidative dehydrogenation(CL-ODH)to ethylene is a new technology for converting ethane to ethylene.In the current study MeO/LaCoO_(3)(MeO=Fe_(2)O_(3),NiO or Co_(2)O_(3))composite metal oxides were prepared via citrate gel and impregnation methods,and used as oxygen carriers for CL-ODH.X-ray diffraction results indicated that all oxygen carriers had a perovskite structure even after eight redox cycles.Under a reaction temperature of 650°C,a reaction pressure of 0.1 MPa,and a weight hourly space velocity(WHSV)of 7500 mL/(g·h),ethane conversion over Co_(2)O_(3)/LaCoO_(3) reached 100%and ethylene selectivity reached 60%,both of which were better than corresponding values attained over Fe_(2)O_(3)/LaCoO_(3) and NiO/LaCoO_(3).Ethylene selectivity remained stable for 80 cycles over Co_(2)O_(3)/LaCoO_(3),then decreased gradually after 80 cycles.X-ray photoelectron spectroscopy results and evaluation results indicated that lattice oxygen and O_(2)2-had a direct relationship with ethane conversion and ethylene selectivity.Co_(2)O_(3)/LaCoO_(3) exhibited a strong capacity to release and absorb oxygen,mainly due to interaction between Co_(2)O_(3) and LaCoO_(3).

NiO-Doped Fe_(2)O_(3)/MgO Properties for the Chemical Looping Oxidative Dehydrogenation of Ethane

Ethane chemical looping oxidative dehydrogenation(CL-ODH)to ethylene is a new technology for ethylene preparation.Fe_(2)O_(3)/MgO oxygen carrier was prepared using the co-precipitation method.The influence of added NiO and its different loadings on Fe_(2)O_(3)/MgO were investigated.Then,a series of oxygen carriers were applied in the CL-ODH of the ethane cycle system.Brunauer-Emmett-Teller(BET),X-ray diffractometry(XRD),X-ray photoelection spectroscopy(XPS),and H2-temperature programmed reduction(TPR)were used to characterize the physicochemical properties of these oxygen carriers.It was confirmed that an interaction between NiO and Fe_(2)O_(3) occurred based on the XPS and H2-TPR results.Based on the CL-ODH activity performance tests conducted in a fixed-bed reactor,it was revealed that ethylene selectivity was significantly improved after NiO addition.Fe_(2)O_(3)-10%NiO/MgO showed the best activity performance with 93%ethane conversion and 50%ethylene selectivity at a reaction temperature of 650℃,atmospheric pressure,and space velocity of 7500 mL/(g·h).

Impact of Fenton and ozone on oxidation of wastewater containing nitroaromatic compounds

Fenton and ozone treatment was investigated at laboratory scale for the degradation of aqueous solutions of nitrobenzene （NB）. Effects of reactants concentration （O3, H2O2, and Fe（Ⅱ））, temperature, and pH on NB degradation were monitored. Reaction kinetic of these processes was also assessed. A rapid reaction took place for Fenton process at higher initial concentration of H2O2, higher temperatures, and more acidic conditions （pH 3）. Similarly, ozonation reaction exhibited rapid rates for higher ozone dose, higher temperatures, and more basic conditions （pH 11）. Complete NB degradation in 65 min was achieved using Fenton process. The conditions of complete elimination of 100 mg/L of initial NB concentration, were 250 mg/L of H202 concentration, pH 3, and 10 mg/L of Fe（Ⅱ） concentration. Under these conditions, 55% organic carbon elimination was achieved. Total organic carbon mineralization was attained in 240 rain reaction time by Fenton process with 900 mg/L of H202 concentration, and 30 mg/L of Fe（Ⅱ） concentration. Fenton reaction showed a pseudo-first order kinetic; the reaction rate constant was ranged from 0.0226 to 0.0658 min^-1. Complete NB degradation was also achieved for an ozone dose of the order of 2.5 g/L. The ozonation was studied at different ozone doses, different initial pH （7-11） and at different temperatures （15-35℃）. NB ozonation kinetic was represented by a bi-molecular kinetic model which was reduced to pseudo-first order kinetic. The pseudo-first order reaction rate constant was determined to increase at 20℃ from 0.004 to 0.020 min^-1 as the used ozone increased from 0.4 to 1.9 g/L.

Study on Decoloration of Acidic Scarlet GR by Pyrolusite Oxidation under an Acid Condition

Decoloration of acidic scarlet GR by pyrolusite is studied in this paper. The effects of pH in solution, dosage and granularity of pyrolusite, reaction temperature, and vibration speed on decoloration efficiency are discussed. According to experiment results, the decoloration efficiency may exceed 95% for 40 mg/L GR solution by pyrolusite, pH is most important among all factors which impact the decoloration of acidic scarlet GR. Dosage and granularity of pyrolusite, reaction temperature, and vibration speed have a little benitfit on decoloration. The high decoloration efficiency and low removal efficiency of COD as well as FT-IR spectra of products between pyrolusite and acidic scarlet GR indicate that acidic scarlet GR undergoes the redox reaction on the interface of mineral and its chromophore is oxidated and decolored, but it is not removed thoroughly by oxidation.

Synthesis of Nicotinic Acid by Potassium Dichromate Oxidation

Nicotinic acid was synthesized from 3 methylpyridine with potassium dichromate as the oxidant. The reaction conditions, the product separation and analysis were studied. The results indicate that under the certain reaction conditions, the yield of nicotinic acid can reach 67.4%, the conversion can reach 99.7% and the selectivity can be as high as 99.8%. The final product has a high purity.

In situ characterization of natural pyrite bioleaching using electrochemical noise technique

An in situ characterization technique called electrochemical noise（ECN） was used to investigate the bioleaching of natural pyrite.ECN experiments were conducted in four active systems（sulfuric acid,ferric-ion,9k culture medium,and bioleaching solutions）.The ECN data were analyzed in both the time and frequency domains.Spectral noise impedance spectra obtained from power spectral density（PSD）plots for different systems were compared.A reaction mechanism was also proposed on the basis of the experimental data analysis.The bioleaching system exhibits the lowest noise resistance of 0.101 MΩ The bioleaching of natural pyrite is considered to be a bio-battery reaction,which distinguishes it from chemical oxidation reactions in ferric-ion and culture-medium（9k） solutions.The corrosion of pyrite becomes more severe over time after the long-term testing of bioleaching.

Iron in Water: Study of Iron Removal Kinetics in Chemically Reconstituted Waters: Application to Groundwater of South Pout (PS2 Site)

The goal of this topic is a synthesis of the main characteristics of iron in groundwater and the oxidation process used to remove it. Indeed, the kinetics of chemical oxidation of iron (II) was examined with reconstituted water (distilled water + iron sulphate) and proceeded to the application in the groundwater samples taken from South Pout (Senegal) precisely in the drilling PS2. The sources of iron are natural or anthropogenic. In Senegalese waters, its content is variable and sometimes exceeds the standards of potability. Despite the diversification of iron removal process, chemical oxidation is the most used solution in drinking water treatment plants in Senegalese rural areas. Applied oxidation processes such as aeration and chlorination, however, are insufficient to produce drinking water with an iron concentration in accordance with standards of potability.

Exogenous Nitric Oxide Involved in Subcellular Distribution and Chemical Forms of Cu^(2+) Under Copper Stress in Tomato Seedlings

Nitric oxide（NO）,a bioactive signaling molecule,serves as an antioxidant and anti-stress agent under abiotic stress.A hydroponics experiment was conducted to investigate the effects of sodium nitroprusside（SNP）,a NO donor,on tomato seedlings exposed to 50 μmol L-1CuCl 2.The results show that copper is primarily stored in the soluble cell sap fraction in the roots,especially after treatment with Cu＋SNP treatment,which accounted for 66.2% of the total copper content.The copper concentration gradually decreased from the roots to the leaves.In the leaves,exogenous NO induces the storage of excess copper in the cell walls.Copper stress decreases the proportion of copper integrated with pectates and proteins,but exogenous NO remarkably reverses this trend.The alleviating effect of NO is blocked by hemoglobin.Thus,exogenous NO is likely involved in the regulation of the subcellular copper concentrations and its chemical forms under copper stress.Although exogenous NO inhibited the absorption and transport of excess copper to some extent,the copper accumulation in tomato seedlings significantly increased under copper stress.The use of exogenous NO to enhance copper tolerance in some plants is a promising method for copper remediation.

Hydrophobic Ti_xO_y-C_mH_n Nanoparticle Film Prepared by Plasma Enhanced Chemical Vapor Deposition

The hydrophobic films of TixOy-CmHn. deposited from mixture gases of titanium isopropoxide （TTIP） and oxygen by plasma enhanced chemical vapor deposition （PECVD） were investigated. The films were investigated by scanning electron microscope （ SEM ）, transmission electron microscope （ TEM ）, Fourier transform infrared spectrometer （ FTIR）, X-Ray diffraction （ XRD ）, element analysis （ EA ）, ultraviolet visible spectrometer （ UV-Vis）, and water contact angle （WCA）. The results reveal that the surface of the films is formed by mierosized papillaes aggregated by inorganic and organic phases of complex nanoparticles with size from 50 nm to 200 nm when the discharge power is increased from 40 W to 150 W. All fdms demonstrate the strong broad of Ti-O-Ti stretching vibration at 400 -800cm-1, -CH bending vibration at 1 388 cm -1, and broadening -OH stretching vibration at 3 000-3500 cm-1 With the increase of the discharge power, the asdeposited film changes from amorphous to crystallization. The WCA of the film can be as high as 160°, indicating the hydrophobicity. The films show a similar ultraviolet absorption property as the bulk TiO2 film. The composition of the composition of film deposited at 150 W can be formulated as Tio.302-C1.5H3. Therefore, the composition formula of this hydrophobic film could be expressed as TiO2-C5H10O4.7. It is believed that the complex micro/nano structures of TiO2 and C5H10O4.7 residues are responsible for the observed hydrophobicity and the ultraviolet absorption property of the film.

Preparation and photocatalytic activity of PANI/TiO_2 composite film

A PANI/TiO2 composite film deposited on the glass surface was successfully prepared using sol-gel dip-coating technique and chemical oxidation method. The film was characterized using XRD, AFM, and UV. The result showed that the TiO2 film consists of both cuboid-shaped and anatase-phased TiO2 nanoparticles. The average grain size of TiO2 in the film was approximately 20 nm. After coating with PANI, the particle was changed into irregular spherical-shaped and the size was increased up to approximately 35 nm in diameter. UV-Vis spectroscopy analysis indicated that the coating of TiO2 with PANI would result in an enhancement of photocatalytic efficiency and an extension of the photoresponse of TiO2. The band gap of the PANI/TiO2 film was 3.18 eV. The photocatalytic property of the film was evaluated by the degradation of rhodamine-B. It was found that 67.1% and 83.2% of rhodamine-B could be degraded under sunlight and UV irradiation within 120 min using the PANI/TiO2 composite t-tim as photocatalyst.

Controlled high-density interface engineering of Fe_(3)O_(4)-FeS nanoarray for efficient hydrogen evolution

The rational design of double active sites system is vital for constructing high-efficiency iron sulfides electrocatalysts towards hydrogen evolution reaction(HER) in alkaline media. However, it remains a challenge to controllably create the high-density interface of double sites for optimal synergistic effect.Herein, we reported a simple chemical oxidation-induced surface reconfiguration strategy to obtain the interface-rich Fe_(3)O_(4)-FeS nanoarray supported on iron foam(Fe_(3)O_(4)-FeS/IF) using FeS nanosheets as precursors. The abundant Fe_(3)O_(4)-FeS interfaces could improve the dispersion of active sites and facilitate the electron transfer, leading to enhanced hydrogen evolution efficiency. And meanwhile, by altering the oxidation temperature, the content of S and O could be effectively controlled, further achieving the ratio optimization of Fe_(3)O_(4)to FeS. Synchrotron-based X-ray absorption near-edge structure, X-ray photoelectron spectroscopy and ultraviolet photoemission spectroscopy consistently confirm the changes of electronic structure and d-band center of Fe_(3)O_(4)-FeS after chemical oxidation. Consequently, Fe_(3)O_(4)-FeS/IF exhibits excellent alkaline HER activity with a low overpotential of 120.8 mV to reach 20 mA cm^(-2),and remains stable ranging from 10, 20 to 50 mA cm^(-2) for each 20 h, respectively. Therefore, the facile and controllable chemical oxidation may be an effective strategy for designing high-density interfaces of transition metal-based sulfides towards alkaline HER.

In-situ remediation of deep petroleum-contaminated soil injection

A computational fluid dynamics(CFD)numerical simulation and field experiment were used to investigate optimal operating parameters of high-pressure jet grouting equipment and clarify the boundary law of the injection area in the remediation process.The response surface optimization design results show that the optimal injection pressure is 30 MPa,rotation speed is 23 r/min,commission speed is 30 cm/min,and the optimal injection diameter is 147.3 cm.Based on the CFD numerical simulation,the ratio of the injection core,turbulent zone,and seepage zone is approximately 1∶4∶2.The distribution law of jet core,turbulence zone and seepage zone at different cross-sections under 30 MPa operating conditions is as follows:The jet core radius is approximately 100 mm,the turbulence zone is mainly distributed at 100 to 500 mm,the seepage zone is mainly distributed at 500 to 700 mm,the seepage zone could be completed within 2 h,and the proportion of the three boundary zones in the injection zone is similar to that of the numerical simulation.This study provides theoretical parameters and practical reference for the remediation of deep pollution via in-situ chemical oxidation in the Loess Plateau soil environment.

Oxidative Treatment of Some Reactive Dyes by Fenton Reagent

Nine kinds of reactive dye solutions: Reactive K -2RL, H-E2R, X-6B1Y, HE-4G, X-3B, K-2R, H - E7B, X -4RN and S - F3B were treated by using Fenton reagent. While the concentration of dye is 400 mg/L, the FeSO4 dosage 100 -180 mg/L, H2O2 240 -540 mg/L, that is the stoichiometric numbers of Fe2+ and H2O2 are between 1: 9 - 1:12, pH = 3, reaction tune In, temperature 25℃, the colority removal efficiency reach more than 95%, the COD removal efficiency 65% -85%, and the TOC removal efficiency 70.2%. By comparing UV-VIS absorption spectrum before and after treatment, it further shows that decomposition effect of Fenton reagent on these nine kinds of reactive dyes is satisfactory.

Study of lithium/polypyrrole secondary batteries with Lithium as cathode and polypyrrole anode

Lithium/polypyrrole （Li/PPy） batteries were fabricated using lithium sheet as cathode, PPy as anode, microporous membrane polypropylene/polyethylene/polypropylene （PP/PE/PP） composite as separator and LiPF6/ethylene carbonate-dimethyl carbonate-methyl ethyl carbonate （EC-DMC-EMC） as electrolyte. Polypyrrole was prepared by chemical polymerization. Certain fundamental electrochemical performances were investigated. Properties of the batteries were characterized and tested by SEM, galvanostatic charge/discharge tests, cyclic voltammetry （CV）, and a.c. impedance spectroscopy. The influences of separator, morphology, and conductivity of PPy anode, cold-molded pressure, and electric current on the performances of the batteries were studied. Using PP/PE/PP membranes as separator, the battery showed good storage stability and cycling property. The conductivity of materials rather than morphology affected the behavior of the battery. The higher the conductivity, the better performances the cells had. Proper cold-molded pressure 20 MPa of the anode pellet would make the properties of the cells good and the fitted charge/discharge current was 0.1 mA. The cells showed excellent performance with 97%-100% coulombic efficiency. The highest discharge capacity of 95.2 mAh/g was obtained.

Surface magnetization of siderite mineral

Surface self-magnetization of siderite is achieved by generating ferromagnetic substance on the surface of siderite by adjusting slurry temperature,pH value,stirring rate and reaction time.No addition of any iron-containing reagent is required.The temperature of 60 ℃,NaOH concentration of 0.10 mol/L;stirring rate of 900 r/min and the reaction time of 10 min are the optimal conditions.The results show that the siderite recovery in magnetic separation increased from 26.9% to 88.8% after surface magnetization.Magnetization kinetic equation is expressed as 1 [1(e0.269)]1/3 = Kt.Activation energy for the magnetization reaction is 4.30 kJ/mol.VSM,SEM and XPS were used to characterize the siderite,and results show that the saturated magnetization(rs) of siderite increased from 0.652 to 2.569Am2 /kg,the magnetic hysteresis was detected with a coercive force of 0.976 A/m after magnetization;Fe2P3/2 electron binding energy changed which reflects the valence alteration in iron on the surface and the formation of ferromagnetic Fe3O4.

Temperature effect on the kinetics of persulfate oxidation of p-chloroaniline

The kinetics of heat-facilitated persulfate oxidation of p-chloroaniline（PCA） in aqueous solutions was measured at five different temperature conditions and at four different oxidant concentrations.The PCA degradation was found to follow a pseudo-first-order decay model when the persulfate was excessive.The pseudo-first-order rate constants of PCA degradation by persulfate（50 mmol/ L） at pH 7.0 are 0.12×10^-4,0.28×10^-4,0.43×10^-4,0.83×10^-4,1.32×10^-4 s^-1 at 10,20,30,40 and 50℃,respectively. Under the above reaction conditions,the reaction has activation energy of 49.97 kJ/mol.The observed rate was found to be function of temperature and oxidant concentration.Raising temperature and increasing persulfate concentration can significantly accelerate the PCA degradation.