Solvent free oxidation of alcohols catalyzed by KMnO4 adsorbed on Kieselguhr

Efficient and selective oxidation of primary and secondary alcohols to the corresponding aldehydes and ketones catalyzed by potassium permanganate supported on Kieselguhr reagent under solvent free conditions are reported.     

Immobilizing chromium in stainless steel slags with MnO addition

This work investigates the stabilizing impact of MnO on the leaching behavior of hazardous Cr-containing CaO-SiO₂-Al₂O₃-Cr₂O₃-MnO stainless steel slags after equilibrating at various elevated temperatures and evaluates the potential immobilization of Cr into a MnCr₂O₄ spinel phase from the existing Cr₂O₃ phase. The MnCr₂O₄ spinel phase was found to be an excellent Cr-stabilizer in stainless steel slags, where the leaching tendency of potentially hazardous Cr-related ions decreased with higher MnO content and lower equilibration temperatures within the range of 0 to 15 mass pct. and 1500 to 1300°C, respectively. Thermodynamic calculations by conducting the phase stability diagram also showed that the MnCr₂O₄ spinel phase was relatively stable and the Ca₃Si₂O₇ (Ca_3-xMn_xSi₂O₇) phase was relatively unstable compared with other crystal phases in acid extractant with pH value of 3.2. Combined with the scanning electron microscopy and X-ray powder diffraction results along with the thermodynamic calculations, the leached Cr-related ions was predominantly originating from the unstable amorphous glass phase.     

High temperature corrosion mechanisms and effect of alloying elements for materials used in waste incineration environment

Corrosion products on two typical materials, SA213-T12 steel and alloy 625 exposed to the actual combustion gas, were analyzed in addition to laboratory tests for penetration of corrosive matter. It has been clarified that corrosion products of oxides containing a little chlorides and sulphides show lamellar structures and that at the alloy-scale interface, chlorination, sulphidation, and oxidation occur under a low P_O2-high P_Cl2 condition. The formation of scale structures and the effect of corrosion-resistant alloying elements can be explained according to the stability tendencies of metals, chlorides, and oxides in the M-Cl-O equilibrium diagrams. The severity of corrosion environments at the interface is influenced by the penetration extent of corrosive matters through deposits and scales, and the protective effects of oxide films derived from alloying elements play an important role in preventing the corrosion. On the other hand, it has been shown that thermal fluctuation characterized in this kind of environment makes the lamellar scale structures and sometimes breaks and peels off the scale, and thus accelerates the corrosion. On the basis of the above mentioned knowledge, a new corrosion model is presented.     

城市居民污水处理自动控制系统

针对以三沟式氧化沟为核心的污水处理工艺的特点,采用由工控机(IPC)与可编程控制器(PLC)组成的自动控制系统,实现了对污水处理全过程的自动控制。本文首先讨论了文章中所采用的进化工艺,接着就自动控制系统的控制系统和软件设计进行了探讨。     

Sol–gel alumina environmental barrier coatings for SiC grit

SiO₂ surface film is insufficient to protect SiC from the oxidation at widely varying partial pressures of oxygen, in particular in the presence of water vapor (e.g. in gas turbines) and also in other environments, e.g. during brazing for hard “tipping” of turbine blades. This work demonstrates that sol–gel alumina, coated on 0.5 mm coarse SiC grit, may form an acceptable, up to 10 μm thick “environmental barrier coating” EBC for some of these applications. The sol–gel has advantages over other methods (such as CVD) is the simplicity and low cost. We have used NH₄OH pre-treatment to hydroxylate surface of SiC prior to applying alumina coating. Such modified SiC/SiO₂ surface helped to deposit the positively charged alumina sol, and thus allowed to build thick coatings on the SiC grit. There is some indication that these coatings partially convert to mullite through reaction at the interface with the native silica on SiC. Oxidation resistance tests at 1200 °C were performed to show effectiveness of such coated SiC grit.     

放射性铌铁精矿中铀钍脱除及分离

通过对国内某企业进口放射性铌铁精矿进行工艺矿物学分析,确定该精矿的主要矿相为烧绿石,同时伴生钛铁矿和白云母,矿石中放射性元素U和Th的含量分别为0.27%和1.03%。针对该铌铁精矿,探索H2SO4-Fe(Ⅲ)、H2SO4-HF-H2O2、H2SO4-HF、H2SO4-HF-H2O2-(NH4)2CO3体系中U和Th的浸出及分离效果,最终确定H2SO4-HF-H2O2-(NH4)2CO3多段浸出工艺能有效实现U和Th的脱除与分离。U、Th的脱除率分别为100%和80%。基于研究提出了铌铁精矿U、Th脱除及分离工艺流程。     

基于流固耦合作用的砂岩地浸采铀效果数值模拟分析

为探究低渗砂岩铀矿在不同因素下的产量变化情况,根据储层有效应力与渗流特性的关系,建立有效应力-渗流数值模型。通过日产水量分析流固耦合作用下储层的产量变化规律,并结合变异系数法分析注入压力、初始渗透率和井间距对产量的影响。研究表明：考虑流固耦合作用下的储层产量会更快进入稳定状态,产量更高;应力敏感性系数越大,有效应力减小对地层渗透率影响越明显。注入压力越大,地层有效应力减小区域下降幅度增大,使地层渗透率增大区域升高幅度增大,导致产量逐渐增多;流固耦合作用下产量随着初始渗透率增大而增多且增长速度较快;流固耦合作用下,随着井间距的增大,注采井间有效应力减小的影响减弱,注采井间渗透率增大趋势也在下降,导致产量逐渐降低。结合各因素变异系数变化可得,注入压力对产量效果影响更明显。本研究有助于建立完整的砂岩铀矿地浸采铀生产方案。     

贫液除杂与污水零排放的试验研究

根据仓上金矿生产实际情况,探讨了贫液除杂质的途径及除杂后对浸出效果的影响,为仓上金矿实现氰化污水零排放提供了基础资料。     

锌精矿常压浸出与加压浸出工艺比较

比较了常压浸出与加压浸出两种工艺的机理、流程、技术经济指标、投资以及存在的问题。试验和生产数据表明,加压浸出在技术上和工艺上都更具有吸引力。     

低品位氧化锌粉矿制粒及碱性浸出

小于2 mm的氧化锌矿(含锌5.17%)与5%的水泥混合,制粒并固化,所得颗粒直径5~8 mm。固化3天、10天、45天的颗粒用碱性溶液浸出,最大浸出率分别为92.2%、87.3%、72.9%。减少固化时间能够缩短反应时间、增加颗粒中锌的溶解以及减少浸出剂中初始锌浓度的影响。实验表明颗粒最少需固化3天。动力学研究表明浸出过程受浸出剂通过脉石层的扩散控制,表观速率常数分别为3.51×10-2d-1、8.09×10-3d-1和4.74×10-3d-1。