010医用制氧粉氧的生物效应及其对重要脏器毒性的观察

010医用制氧粉(以下简称制氧粉)是一种投入水中能立即产生氧气的化学性产氧粉剂。国外于1982年有研制报告及商品,国内于1985年首先由华中理工大学化学系王海龙、钱晓良合成。本实验观察制氧粉氧急性吸入后的生物效应及对心血管、呼吸道、肝、肾等重要脏器的影响。 一、方法与结果 制氧粉产氧的方法:将该粉的两种成份按一定比例(产氧底物:催化剂=100:1,系重量比)投入水中(加水量则按产氧底物20份加水1份),所产氧气用纯氮混合成一定比例后供动物实验用。对照组用医用钢瓶氧(简称医用氧)。

Process control technology of low NO_x sintering based on coke pretreatment

Process control is an effective approach to reduce the NOx emission from sintering flue gas.The effects of different materials adhered on coke breeze on NOx emission characteristics and sintering performance were studied.Results showed that the coke breeze adhered with the mixture of CaO and Fe2O3 or calcium ferrite significantly lowers the NOx emission concentration and conversion ratio of fuel-N to NOx.Pretreating the coke with the mixture of lime slurry and iron ore fines helped to improve the granulation effect,and optimize the carbon distribution in granules.When the mass ratio of coke breeze,quick lime,water and iron ore fines was 2:1:1:1,the average NOx emission concentration was decreased from 220 mg/m3 to 166 mg/m3,and the conversion ratio of fuel-N was reduced from 54.2%to 40.9%.

Preparation of AgSnO_2 composite powders by hydrothermal process

Silver-tin oxide powders were synthesized by the hydrothermal method with Ag(NH_3)_2^+ solution and Na_2SnO_3 solution as raw materials and Na_2SO_3 as reductant. The precipitation conditions of Na2SnO3 solution and the reduction conditions of Ag(NH_3)_2^+ were also investigated. The powders prepared were characterized by differential thermal analysis (DTA), X-ray diffraction analysis (XRD), scanning electron microscope (SEM) and energy spectrum analysis. The results show that pH value of the solution is a key parameter in the formation of Sn(OH)_4 precipitate and the reduction reaction of Ag(NH_3)_2^+ can release H+ ions, which results in synchronous precipitation of Sn(OH)_6~2- as Sn(OH)_4. The reduction of Ag(NH_3)_2^+ and precipitation of Na_2SnO_3 occur simultaneously and the coprecipitation of silver and tin oxide is reached by the hydrothermal method. The silver-tin oxide composite powders have mainly flake shape of about 0.3 μm in thickness and there exists homogeneous distribution of tin oxide and silver in the powder synthesized.

Preparation of titanium powders by calciothermic reduction of titanium dioxide

To develop an effective process for titanium powders production, a calciothermic reduction process of pigment titanium dioxide （w（TiO2）〉98%）, based on the preform reduction process （PRP）, was investigated by means of XRD, SEM and EDS. In this process, the mixture of TiO2 powder and CaC12 was pressed into pieces as feed preform and was reduced by calcium vapor. Titanium powders was recovered after leaching from the reduced preform with hydrochloric acid and deionized water. The results indicate when the mass ratio of CaC12 to TiO2 is about 1：4 and at a constant temperature of 1 273 K for 6 h in vacuum furnace, titanium powders with 99.55% purity by EDS analysis and irregular shape （8-15 μm in particle size） are obtained.

Agglomeration Control of Ultrafine Y_2O_3-ZrO_2 and (MgO, Y_2O_3)-ZrO_2 Powders Synthesized by Coprecipitation Process

Chemical coprecipitation was used to produce ultrafine and easily sinterable Y2O3-stabilized and （Y2O3,MgO）-stabilized ZrO2 powders. Six precipitation processes for preparation of ZrO2-based ultrafine powders were designed separately, meanwhile different techniques used to control the agglomeration formation were proposed. By means of TEM, SEM, Raman spectroscopy and IR spectroscopy, the mechanisms of agglomeration control in the precipitation processes and post-precipitation and drying process were investigated. The experimental results show that adding appropriate anion surface active agents （such as PAA1460） or polymer （PEG1540 matching with PEG200） in aqueous solution systems during precipitation processes could reinforce charge effect and location effect for gel particles interface. Adding wetting agents to wet gels washing with distilled water during drying process could change interface structure of gel particles and decrease surface tension between gel particles. The agglomeration control in the precipitation, post-precipitation and drying processes had remarkable influence on the characteristics of powders. By adding various macromolecules in the processes, the agglomeration state could be controlled efficiently, and the characteristics of powders were improved.

Preparation and sintering properties of zirconia-mullite-corundum composites using fly ash and zircon

Zirconia-mullite-corundum composites were successfully prepared from fly ash,zircon and alumina powder by a reaction sintering process.The phase and microstructure evolutions of the composite synthesized at desired temperatures of 1 400,1 500 and 1 600°C for 4 h were characterized by X-ray diffractometry and scanning electronic microscopy,respectively.The influences of sintering temperature on shrinkage ratio,apparent porosity and bulk density of the synthesized composite were investigated.The formation process of the composites was discussed in detail.The results show that the zirconia-mullite-corundum composites with good sintering properties can be prepared at 1 600°C for 4 h.Zirconia particles can be homogeneously distributed in mullite matrix,and the zirconia particles are around 5μm.The formation process of zirconia-mullite-corundum composites consists of decomposition of zircon and mullitization process.

Preparation and Characterization of Sodium Sulfate/Silica Composite as a Shape-stabilized Phase Change Material by Sol-gel Method

A sodium sulfate （NaeSO4）/silica （SiO2） composite was prepared as a shape-stabilized solid-liquid phase change material by a sol-gel procedure using Na2SiO3 as the silica source. Na2SO4 in the composite acts as a latent heat storage substance for solid-liquid phase change, while SiO2 acts as a support material to provide structural strength and prevent leakage of melted NazSO4. The microstructure and composition of the prepared composite were characterized by the N2 adsorption, transmission electron microscope （TEM）, scanning electron microscope （SEM）, Fourier transform infrared spectroscopy （FTIR） and X-ray diffraction. The results show that the prepared Na2SOJSiO2 composite is a nanostructured hybrid of NazSO4 and SiO2 without new substances produced during the phase change. The macroscopic shape of the NazSO4/SiO2 composite after the melting and freezing cycles does not change and there is no leakage of Na2SO4. Determined by differential scanning calorimeter （DSC） analysis, the values of phase change latent heat of melting and freezing of the prepared NazSO4/SiO2 （50%, by mass） composite are 82.3 kJ.kg i and 83.7 kJ.kg-1, and temperatures of melting and freezing are 886.0 ℃ and 880.6 ℃, respectively. Furthermore, the Na2SOJSiO2 composite maintains good thermal energy storage and release ability even after 100 cycles of melting and freezing. The satisfactory thermal storage performance renders this composite a versatile tool for high-temperature thermal energy storage.

Zinc leaching from electric arc furnace dust in alkaline medium

Physical and chemical properties of electric arc furnace （EAF） dust from Tianjin seamless Pipe Company were measured and analyzed. The zinc leaching tests in alkaline medium were carried out under variation of leaching agent concentration, leaching temperature, leaching cumulative time and solid-to-liquid ratio. The thermodynamics and kinetics of the zinc leaching process were also analyzed. The results show that the EAF dust contains 10% （mass fraction） zinc and the median particle size is 0.69 μm. The zinc recovery of 73.4% is obtained tinder the condition of 90 ℃, 6 mol/L NaOH, and 60 min leaching time. With the increase of concentration of NaOH and the cumulative time, zinc leaching will be significantly increased. The kinetics study demonstrates that the leaching reaction is chemically controlled and the reaction activation energy is 15.73 kJ/mol.

Fabrication and Characterization of Alumina/CNTs Nanocomposite Powders, by CCVD Method and Investigation of the Parameter Involved

Ceramics in general and particularly alumina （Al2O3） are important materials in various industries, but the main problem with these materials is related to some of their mechanical properties including low resistance against mechanical shock （hardness-toughness）, which makes them to be so brittle, and possession of high degree of porosity which reduces their strength and gives them fragile characteristics. Researchers report indicates that the presence of the second phase with suitable properties can improve some of the mechanical properties of these materials and optimize their characteristic. Carbon nanotubes with unique physical characteristics such as large aspect ratio, high strength and Young＇s modulus and improved thermal properties could be suitable candidates for this purpose. In this study, the growth of multi wall carbon nanotubes （MWCNTs） on the alumina support as the matrix of the composite has been carried out, using catalytic chemical vapor deposition （CCVD） method in which the iron nanoparticles has been selected as catalyst materials. Ethylene gas is used as feed materials for carbon source and argon as the carrier gas. In order to achieve a more comprehensive results, we have investigated the effects of some fabricating parameters like catalyst particle size, its weight percentage related to support material, alumina and to the some synthesizing temperature gases flow rate. Fabricated ceramics composites samples structures were analyzed using SEM images as well as Raman scattering spectra and X-ray diffraction pattern.

Preparation of nano-TiO_2 photocatalysts and their decomposition activity in phenol-contaminated water

ZiO2 was prepared by the hydrolyzation method in （NH4）2SO4-modified TiCl4 solution, and TiO2 photocatalysts were obtained by accelerating the precipitation of TiO2 powder in a high-temperature water bath. The photocatalysts were characterized by Brunauer-Emmett-Teller （BET）, X-ray diffraction （XRD）, Raman spectrum and UV-Vis （Ultraviolet-Visible） spectrometry techniques, and the photocatalytic activity in phenol-contaminated water was investigated. The results showed that photocatalysts calcined at 400 ℃ had a specific surface area of 138.2 m^2/g and an average particle size of 9 nm, and a significant increase in thermal stability of anatase phase. At the calcination temperature of 700 ~C, the crystal form of TiO2 started to change into rutile （anatase： 97%, rutile： 3%）. The activity of TiO2 photocatalysts prepared with （NH4）2SO4-modified TIC14 solution was markedly stronger than that without （NH4）2SOg-modified TIC14 solution. Maximal photocatalytic activity was observed at the mole ratio of Ti：（NH4）2SO4= 1：2, the water-bath temperature of 90℃ and the calcination temperature of 700 ℃.