Biodegradation Kinetics and Mechanism of a Typical Coal Gasification Pollutant: Quinoline

A strain Pseudomonas sp.PP1 was isolated from activated sludge and characterized by morphological observation,biochemical and physiological identification as well as 16 S rRNA gene sequence analysis.It was a gram-negative,non-motile,rod-shaped with colonies which were white,opaque,small and wrinkled on solid quinoline-MSM.The strain was negative for catalase,gelatin liquefaction,M.R and V.P tests and was unable to reduce / restore nitrate.The 1406 bp 16 S rRNA gene fragment of PP1 was more than 99% identical to the Pseudomonas sp.Biodegradation of quinoline as single substrate was conducted in batch experiments at different temperatures（ 15- 40 ℃） and p H values（ 5- 10）.The results indicate that the optimum conditions for the degradation of quinoline by PP1 were 30 ℃ and p H 7.Pseudomonas sp.PP1 was able to degrade 97.1%,95.4%,94.8%,63.6% and 40.4% quinoline when initial concentrations of quinoline were 50,100,200,300,and 400 mg / L,respectively,and lag phases were prolonged from 2 h to 10 h.The maximum degradation rate（ q） was obtained at an initial quinoline concentration（ S0） of about 100 mg/L with q of 0.082.The experimentally obtained q values at various initial S0 were fitted by Haldane model,Yano model,Aiba model,Edward model and Webb model,and the results demonstrated that Haldane model gives the best fit for strain PP1 with coefficient of determination,R^2= 0.9124 and SDavg= 0.0113208.Five metabolic intermediates were identified by high performance liquid chromatograph（ HPLC） and GC / MS.Finally,a possible pathway containing 5,6-dihydroxy-2-oxo-1,2-dihydroquinoline as an intermediate was proposed for the first time.     

Modified-starch consolidation of alumina ceramics

The alumina ceramics with the homogeneous microstructure and the higher density were fabricated via the modified-starch consolidation process by 1.0 wt% of a modified starch as a consolidator/ binder. The swelling behavior of the modified oxidized tapioca starch was analyzed by optical microscope, and two other corn starches （common corn starch and high amylose corn starch） were also analyzed for comparison. The modified starch used as a binder for the consolidation swelled at about 55 ℃, began to gelatinize at 65 ℃ and then was completely gelatinized at 75 ℃. But the corn starches could not be completely gelatinized even at 80 ℃ for 1 h. The high-strength green bodies （10.6 MPa） with the complex shapes were produced. The green bodies were sintered without any binder burnout procedure at 1 700 ℃ and a relative density of 95.3% was obtained for the sintered bodies, which is similar to that of the sintered sample formed by conventional slip casting. In addition, the effect of temperature on the apparent viscosity of the starch/alumina slurry in the process was investigated, and the corresponding mechanism for the starch consolidation was discussed.     

Synthesis and coloring properties of Cd（S1-xSex） pigments by precipitate-hydrothermal method

Cd（S1-xSex） pigments （red to yellow） were synthesized by precipitate-hydrothermal method. The structure, morphology and hue of the powder were characterized by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, energy dispersive X-ray spectroscopy （EDAX） and CIE chromaticity. The optimum synthesis conditions were obtained and reaction mechanism was further analyzed as well. The results show that molar ratio of S to Se, pH value and hydrothermal reaction conditions have great effects on the hues of the pigments. Pigments with vivid hues are obtained under the conditions that pH value is about 13.0, hydrothermal reaction condition is at 140 ℃ for 4 h or at 160 ℃ for 6 h. The reaction mechanism is that Se^2- of Cd（S1-xSex） substitutes S^2- of CdS and then forms a continuous solid solution.     

Properties study and phylogenetic analysis of a bacterial strain with high de-emulsification efficiency

For further practical application,the phylogenetic analysis and de-emulsification properties study of strain XH1 with high de-emulsification efficiency isolated from crude oil contaminated soil in Daqing oil field were conducted with a surfactant-stabilized water-kerosene model emulsion. The factors influencing the de-emulsification efficiency and the generation site of de-emulsification active component of the strain were also investigated. The similarity of 16SrDNA sequences between strain XH1 and Bacillus mojavensis(DQ993678)was 99%. According to the physiological biochemical test,strain XH1 was preliminarily identified as Bacillus mojavensis. The logarithmic growth,stable phase and decline phase of strain XH1 were determined as 14,18 and 28 h,respectively. The best de-emulsification activity emerged after cultivating for 18h,and the complete de-emulsification was achieved at 24 h. The most favorable incubation conditions for de-emulsification occurred with pH of 6.0 at 30 ℃. The de-emulsification capability of strain XH1 was mainly resulted from extracellular metabolites. The above results indicate that strain XH1 has high de-emulsification efficiency and is potential as a commercial de-emulsifier.     

Preparation of p-menthane hydroperoxide from p-menthane in presence of metalloporphyrins

The aerobic oxidation of p-menthane to p-menthane hydroperoxide (PMHP) in the presence of metalloporphyrins was investigated in an intermittent mode under an atmospheric pressure of air. Several important reaction parameters, such as the structure of metalloporphyrin, the air flow rate, and the temperature, were studied. The preliminary mechanism of the aerobic oxidation of p-menthane catalyzed by metalloporphyrins was also discussed. The results show that the reaction is greatly accelerated by the addition of metalloporphyrins at very low concentration, in terms of both the yield and formation rate of PMHP, and the high selectivity of PMHP is maintained during the reaction. Temperature of 120 ℃ and reaction time of around 5 h are the optimal conditions for the best result in the presence of 0.06 mmol/L monomanganeseporphyrins ((p-Cl)TPPMnCl). Furthermore, the yield of PMHP is increased remarkably when the reaction is carried out under programmed temperature compared with the constant temperature. When the reaction is catalyzed by 0.06 mmol/L((p-Cl)TPPMnCl) at the air flow rate of 600 mL/min and 120 ℃ for 4 h, and then the temperature is reduced to 110 ℃, for another 4 h, the yield of PMHP reaches 24.3%, which is higher than that of the reaction at a constant temperature of 120 ℃ or 110 ℃ for 8 h.     

A series of aminoamides used for flotation of kaolinite

N-(2-aminoethyl)-dodecanamide, N-(3-dimethylaminopropyl)-dodecanamide, and N-(3-diethylaminoproyl)-dodecanamide used as collectors were studied for the flotation of kaolinite in the absence of additives at different pulp pHs as well as different collector contents. The effectiveness of the long chain aminoamides on pure kaolinite was demonstrated in laboratory scale flotation tests. The adsorption mechanism of the aminoamides onto kaolinite was investigated through zeta potential determinations and infrared spectrometry. The -98 μm size fractions of kaolinite, taken from Jiaxian Henan of China, were used in flotation. The hydrophilic group size of the aminoamides has a relatively less influence upon the floatability of pure kaolinite. The results suggest either the static-electric force or the coordinating bond adsorption mechanism of the aminoamides onto kaolinite depends on pulp pH.     

Study on the method of recovering and separating indium from residue containing indium

A method of recovering indium from complex smelting residue containing indium was investigated. Indium was extracted by technique of low acid leaching and solvent extraction. The conditions of separating iron and indium were studied and the optimal conditions were determined. When the residue is twoclass-countercurrent leached with 2 mol/L H2SO4 and 30-40 g/L NaC1 at 100 ℃, the leaching rate of indium is 80%. The extraction rate of indium is over 98% and that of iron is less than 5% after it is third-class-countercurrent extracted by P204, and when sulfonated kerosene is used as solvent, acidity in aqueous phase remains the same as that of leaching liquid, and phase is for 1 : 3. Using 2 mol/L HC1 as back-extraction agent, with phase ratio being 5 : 1, by third-class-countercurrent back-extraction, the back-extraction rate of indium is over 99%, but that of iron is very low, which can meet the need of separating indium and iron.     

Effect of one-step aging on microstructure and properties of a novel Al-Zn-Mg-Cu-Zr alloy

The effect of one-step aging temper on the mechanical properties, electrical conductivity and the microstructure of a novel Al-7.5Zn-1.6Mg-1.4Cu-0.12Zr alloy has been investigated. The results indicated that with elevating the aging temperature from 100℃ to 160℃, the aging response rate was greatly accelerated, and the UTS at peak aging condition decreased, while the corresponding TYS increased. However, the electrical conductivity of the alloy became higher. After aging for 24 h at 120℃, the peak UTS and TYS values were achieved as 591 MPa and 541 MPa, respectively; but the alloy achieved a lower conductivity, 20.4 MS/m. When T6 temper was performed at 140℃ for 14 h, the UTS decreased only by 1% of the former, whereas the TYS and the electrical conductivity increased obviously, which were up to 559 MPa and 22.6 MS/m, respectively. The major strengthening precipitates of the peak-aged alloy were GP zones and η′ phase. The precipitates in both the matrix and the grain boundary became coarser with rising aging temperature. There were obvious PFZs along the grain boundary both in T6 conditions aged at 140℃ and 160℃.     

Optimisation of Bio-polyol Production from Cassava Residue Using Ethylene Glycol as the Liquefaction Reagent

Cassava residue was liquefied by using ethylene glycol(EG), ethylene carbonate, propylene carbonate and polyethylene glycol(molecular weight: 400 g/mol) as the liquefaction reagent respectively at the temperature of 130-170 ℃ with sulfuric acid as the catalyst. The influences of liquefaction parameters, such as the type of liquefaction reagents, mass ratio of EG/cassava residue, liquefaction temperature and time on the properties of the products were discussed. The optimum liquefaction conditions were obtained when the mass ratio of EG/cassava residue was 6:1(w/w), the liquefaction temperature was 150 ℃, the liquefaction time was3 h and the mass fraction of concentrated sulfuric acid/EG was 2.5 wt%. The hydroxyl numbers and residue content of the liquefied products at optimal conditions were 1 137 mgKOH/g and 0.43%, respectively. FT-IR spectrum showed that the liquefaction product of cassava residue was polyether polyol and could be used to prepare polyurethane material or alkyd resins.     

Preparation and visible-light photocatalytic property of nanostructu- red Fe-doped TiO2 from titanium containing electric furnace molten slag

Nanostructured Fe-doped titanium dioxide was synthesized from titanium containing electric furnace molten slag （TCEFMS） by using an alkali fusion, followed by a hydrolyzation-acidolysis-cMcination route. The effects of Mkali/slag mass ratio, calcinating temperature, calcinating time, and water/slag mass ratio on the extraction efficiency and purity of products were systematically studied in this paper. It is indicated that the best extraction efficiency of nanostructured Fe- doped titanium dioxide is 99.35%, when the molten slag is calcinated at 700℃ for 1 h with the mass ratio of alkali/molten slag of 1.5：1. The influence of alkali/slag mass ratio on the photocatalytic activity of final products was evaluated by the photodegradation of methyl blue under visible light irradiation. A maximum photodegradation efficiency of 88.12% over 30 min was achieved under the optimum conditions.     

Antibiotic properties of Al2O3 doping silver

The preparation technique and properties of Ag-type inorganic antibiotic material carried by Al₂O₃ were studied. The results show that the material has good antibiotic and safety properties, the acute toxicity taken by stomata is LD ₅₀>8 000 mg/kg (little and big white rats), and the normal quantity in subacute toxicity test is 80 mg/(kg · d). The better mass fraction of doping Ag₂O in antibiotic material carried by Al₂O₃ is 4%–8%, and the optimal sintering temperature is from 1 000 °C to 1 100 °C. Foundation item: Project (2002AA327090) supported by National High Technology Research and Development Program of China     

Sintering and Electronic Conducting Properties of Lao.7Ca0.3CrO3 Perovskite Synthesized by a Glycine-nitrate Process

La0.7 Ca0.3 CrO3 powder consisting of superfine and uniform particles （ 100-200 nm ） were synthesized using a glycine-nitrate process （ GNP ）. The sintering and electronic conducting properties of La0.7 Ca0.3 CrO3 were invetigated in the sintering temperature range of 1 200-1 450 ℃. The desired morphology of the powder significantly improved its sinterability. La0.7 Ca0.3 CrO3 ceramics sintered at 1 250-1 450 ℃ show high relative densities above 95 % . The ceramics sintered at 1 250-1 400 ℃ have very similar electronic conduct- ing properties, providing electronic conductivities around 55 Ω^-1 cm^-1 at a measuring temperature of 800 ℃ . Further increasing the sintering temperature to 1450 ℃ led to an apparent degradation of electronic conducting properties. This research demonstrates the advantage of the GNP in producing La0.7 Ca0.3 CrO3 with respect to the enhanced sintering properties and superior electronic conducting properties.     

Advanced sludge reduction and phosphorous removal process

An advanced sludge reduction process, i.e. sludge reduction and phosphorous removal process, was developed. The results show that excellent sludge reduction and biological phosphorous removal can be achieved perfectly in this system. When chemical oxygen demand ρ（COD） is 332 - 420 mg/L, concentration of ammonia p（NH3-N） is 30 - 40 mg/L and concentration of total phosphorous p（TP） is 6.0 -9.0 mg/L in influent, the system still ensures ρ（COD）〈23 mg/L, ρ（NH3-N）〈3.2 mg/L and ρ（TP）〈0. 72 mg/L in effluent. Besides, when the concentration of dissolved oxygen ρ（DO） is around 1.0 mg/L, sludge production is less than 0. 140 g with the consumption of 1 g COD, and the phosphorous removal exceeds 91 %. Also, 48.4% of total nitrogen is removed by simultaneous nitrification and denitrification.     

Preparation and characterization of Bi4Ti3O12 platelets by a novel low-temperature molten salt system

Bismuth titanate (Bi₄Ti₃O₁₂) platelets were prepared by molten salt method in a new salt system of CaC_l2-NaCl at 650–750 °C, using bismuth nitrate pentahydrate (Bi(NO₃)₃―H₂O) and titanium butoxide (Ti (OC₄H₉)₄) as raw materials. The synthesis temperature of Bi₄Ti₃O₁₂ platelets was decreased to 650 °C from 900–1100 °C. The phase compositions and crystalline morphology of Bi₄Ti₃O₁₂ platelets were investigated by XRD and SEM. The experimental results indicate that Bi₄Ti₃O₁₂ platelets containing tetragonal and orthorhombic phase with the size of 1–3 μm can be synthesized at 650 °C for 2 h, and the orthorhombic phase becomes the dominant phase at 750 °C for 5 h. The size and proportion of Bi₄Ti₃O₁₂ platelets increase with the increment of the calcining temperature and holding time. The proportion of platelets increases to about ninety percent, and the platelets grow up to about 3–10 μm at 750 °C for 5 h from 1–2 μm at 650 °C for 2 h. This technical route provides a new low-temperature molten salt system for preparing platelets by molten salt methods.     

The Properties of YSZ Electrolyte Sintering at 1300 ℃

The properties of yttria stabilized zirconia（YSZ） related to the sintering process were discussed.YSZ nano-powders about 40-100 nm as raw material,the sub-micrometer grain sizes such as 0.4-3 μm in YSZ were gotten by sintering process at 1300 ℃,which was performed at 1000 ℃ for 2 h,then raised the temperature at the rate of 50 ℃ / h to 1400 ℃,then decreased directly to 1300 ℃ in 30 minutes,finally at 1300 ℃ for 5-20 hours.The ratio of bigger grain size becomes larger as the holding time increasing at 1300 ℃.The grains less than 1 μm are about 50%,eg,43.2%,52.2% and 51.1% related to 1300 ℃ holding 5 hours,8 hours and 10 hours,respectively.As YSZ grain size became small,the electrical conductivities did not decrease,even increased,about 0.20 s/cm at 1000 ℃.The reduced sintering temperature and time were benefited to co-fire with the electrodes in electrode-supported SOFCs.     

Technology of black coloring for stainless steel by electrochemical method

The technology of black coloring for stainless steel by electrochemical method was studied. The optimum bath compositions and operating conditions were obtained as follows. 40 - 50 g/L K2Cr2O7, 15 - 20 g/L MnSO4, 15 -20 g/L （NH4）2SO4, 20 -40 g/L H3BO3, 20 -30 g/L additive A, 2 g/L （NH4）6Mo7O24 ; time 9 -20 min; temperature 15 - 30 ℃ ; potential 3 V and current density 1 - 2 mA/cm^2. The effects of the compositions of the bath on the quality of black colored film were discussed. The influences of passivation process on the black coloring velocity and performances of black colored film layer were investigated. The results show that the passivation process can improve the corrosion resistance and the stability to bear color-change; （NH4）2 SO4 can control the black coloring velocity and prolong black coloring bath life remarkably; and additive A can improve the evenness and compactness of black colored film layer. The results of scanning electron microscopy and energy dispersive spectra show that the microstructure is of cylindrical lump, the filling process can decrease the crackles, and the main elements of black colored film are Fe, Cr, Mn and Ni.     

Thermo-analytical study on stainless steelmaking dust

1　INTRODUCTIONStainlesssteelmakingdustisaby productwastegeneratedfromsteelmakingindustry .Itcontainssig nificantamountsofiron ,lead ,nickel,chromium ,etc .Heavymetalmaybeleachedintotheenviron mentbyrainorundergroundwater ,soitisclassifiedashazardouswastesandbannedbeingdisposedinreg ularlandfill[1] .Thevaluablemetalsinthedustcanberecoveredinthewayofdirectrecycling[2 6 ] andtheworthlessdustshouldbetreatedinthewayofvitrifi cation[7] .But,itisnecessarytocommandthether malbehaviorofthedustbe…     

Electroless copper plating process of N, N, N′, N′-tetrakis (2-hydroxypropyl) ethylenediamine system with high plating rate

Electroless copper plating process of N, N, N′, N′-tetrakis (2-hydroxypropyl) ethylenediamine (THPED) chelating agent was researched comprehensively. The results indicate that plating rate decreases with the increase of concentration for THPED, CuSO₄ · 5H₂O and HCHO, pH value and bath temperature. The additive of K₄[Fe(CN)₆] · 3H₂O, 2, 2′-dipyridyl and polyethylene glycol(PEG) decrease plating rate and K₄[Fe(CN)₆] · 3H₂O has a bad effect on deposits quality, but 2, 2′-dipyridyl and PEG make deposits quality improve greatly. Low concentration of 2-mercaptobenzothiozole (2-MBT) increases plating rate and improves deposits quality, but decreases plating rate and worsens deposits quality when 2-MBT reaches 5 mg/L. The optimal conditions of this electroless copper plating process are that the concentration of THPED, HCHO, CuSO₄ · 5H₂O, PEG, 2, 2′-dipyridyl and 2-MBT are 16.8 g/L, 16.0 mL/L, 13.3 g/L, 0.5 g/L, 5.0 mg/L and 2.0 mg/L, respectively, pH value is 12.75, bath temperature is 30 °C. Plating rate reaches 9.54 μm/h plating for 30 min in the bath. The SEM images demonstrate that the surface of copper film is smooth and the crystal is fine. Foundation item: Project supported by Hubei Daye Nonferrous Metal Corporation of China     

Structure and mechanical properties of ZrO2-mullite nano-ceramics in SiO2-Al2O3-ZrO2 system

ZrO2-mullite nano-ceramics were fabricated by in-situ controlled crystallizing from SiO2-Al2O3-ZrO2 amorphous bulk. The thermal transformation sequences of the SiO2-Al2O3-ZrO2 amorphous bulk were investigated by X-ray diffraction, infrared spectrum, scanning electron microscope and differential scanning calorimetric. And the mechanical properties of the nano-ceramics were studied. The results show that the bulks are still in amorphous state at 900 ℃ and the t-ZrO2 forms at about 950 ℃ with a faint spinel-like phase which changes into mullite on further heating. ZrO2 and mullite become major phases at 1 100 ℃ and an amount of m-ZrO2 occur at the same time. The sample heated at 950 ℃ for 2 h and then at 1 100 ℃ for 1 h shows very dense and homogenous microstructure with ball-like grains in size of 20-50 nm. With the increase of crystallization temperature up to 1 350 ℃, the grains grow quickly and some grow into lath-shaped grains with major diameter of 5 μm. After two-step treatment the highest micro-hardness, flexural strength and fracture toughness of the samples are 13.72 GPa, 520 MPa and 5.13 MPa·m1/2, respectively.     

Preparation, Characterization and Visible Light Photocatalytic Activity of Nitrogen-doped TiO2

The N-doped TiO2 polycrystalline powder was synthesized through calcining the hydrolysis prodact of tetra-butyl titanate with ammonia. The photocatalytic activity of N-doped TiO2 powder with anatase phone calcined at 400℃ was 2.7 times higher than that of Degussa P25 for phenol decomposition under visible light. All samples had mesoporoas structures. X- ray photoelectron spectroscopy confirmed that a trace amount of N atoms remained in the anatase polycrystaUine TiO2 powder when calcined at 400 ℃ as substitutional atoms at the oxygen sites. UV-Vis and EPR analyses indicated that oxygen vacancy states were created during the course of N-doped TiO2 powder formation. It is considered that substitutional N atoms, oxygen vacancy, states, large BET surface areas and mesoporoas structure are important facwrs for the N-doped photocatalyst to present a high vis-activity.