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.     

Recovery of Phosphoric Acid from Spent Petrochemical Catalysts

Petrochemical catalysts are widely used in the industry. For the production of cumene, zeolite-based catalysts containing phosphoric acid are applied. Over the time, coking deactivates the surface, and the catalyst has to be exchanged and disposed of. Different process approaches for recycling the phosphoric acid-containing catalysts were investigated. Related preliminary investigations have shown that calcination of the used catalyst is necessary prior to reprocessing. By digesting the catalyst with hydrofluoric acid, ∼96 % phosphate was recovered. However, this process is very costly in terms of process technology. More promising is digestion by basic or acidic routes. Several options are possible here, and digestion with H₃PO₄ proved to be particularly suitable. Here, phosphate yields reached up to 98.8 %, with a positive balance of economic efficiency at the same time. The catalyst can be produced and recycled in the same plant with the same reagents, what constitutes a major breakthrough towards sustainability in industrial catalysis.     

单─银精矿提取银的技术

某单─银矿经浮选所得精矿（％）：Ａｇｌ～２，Ｃｕ≈１，Ｐｂ４～７，ＣａＯ＋ＭｇＯ３０～３５，Ｓ４～７，Ｃ８～９。研究了氰化、硫脲、氨浸等方案对该精矿浸出效果，并从浸出指标等因素进行比较，认为焙烧─预浸─氨浸方案较好，银浸出率＞９７％，铜浸出率９５％。     

Copper hydrometallurgy-current status,preliminary economics,future direction and positioning versus smelting

The heap leaching of oxide copper ores with copper cathode recovery by solvent extraction and electrowinning is now well established as a low-cost method of copper recovery. This technology has recently been applied successfully to mixed oxide and chalcocite ores, notably in Chile at Cerro Colorado, Quebrada Blanca and Zaldivar.Currently, there are significant development efforts underway to try to extend heap leaching to chalcopyrite ores.The success of heap leaching/SX/EW has also led to a revival in the development of hydrometallurgical processes to recover copper from chalcopyrite and other copper concentrates. The current status of copper hydrometallurgy is reviewed and the most commercially attractive potential applications are explored. The advantages and disadvantages of the hydrometallurgical treatment of chalcopyrite concentrates and its preliminary economics are compared with those for the current best practices in copper smelting and refining.     

REACTIONS OF PYRITE IN CATALYTICAL OXIDATION ACID LEACHING SYSTEM

ＲＥＡＣＴＩＯＮＳＯＦＰＹＲＩＴＥＩＮＣＡＴＡＬＹＴＩＣＡＬＯＸＩＤＡＴＩＯＮＡＣＩＤＬＥＡＣＨＩＮＧＳＹＳＴＥＭ￥Ｘｉａ，Ｇｕａｎｇｘｉａｎｇ；Ｔｕ，Ｔａｏｚｈｉ；Ｙａｎｇ，Ｈａｎｌｉｎ；Ｓｈｉ，Ｗｅｉ（ＩｎｓｔｉｔｕｔｅｏｆＣｈｅｍｉｃａｌＭｅｔ...     

微波作用下铝酸钙炉渣非等温浸出动力学

研究了微波作用下铝酸钙炉渣非等温浸出动力学，考察了不同微波辐射功率对炉渣中氧化铝浸出率的影响以及相应微波功率下反应体系温度随时间的变化规律。结果表明：该浸出动力学过程的控制步骤为界面化学反应控制，表观反应活化能为40kJ／mol左右；微波作用可改变反应的频率因子，对反应活化能影响不明显；随着微波辐射功率的增大，频率因子增加，宏观表现出微波功率的增加对反应有促进作用。     

电场作用对提高微生物浸矿性能的影响

在排土场微生物强化浸出过程中,结合电场生物工程技术,以氧化亚铁硫杆菌为研究对象,提出利用电场作用提高微生物浸矿性能的方法,探讨电场作用对微生物生长代谢以及渗流特性的影响。结果表明：电场作用对氧化亚铁硫杆菌生长代谢的影响非常明显,适当的电场可有效强化其生长代谢能力,过高的电流会抑制氧化亚铁硫杆菌生长;电场作用下,排土场孔隙中微生物的渗流能力明显增强,微生物电动渗流效应在渗透率高排土场中尤为明显。     

FeCl3浸取含Au复杂硫化矿的动力学研究

研究了FeCl_3溶液浸取复杂含金硫化精矿中有价金属Cu,Ag,Pb和Zh的过程,考察了主要过程参量对浸取速率的影响.实验数据用非线性回归方法处理,给出动力学模型,说明精矿中Cu的溶解过程由表面化学反应控制,其速率是Fe~(3+)的0.5级和Cl~(-)的零级反应.实验条件下Cu,Ag,Ph和Zn的最终浸取率分别达到96,95,90和91%,超过90%的Fe进入浸取液,总硫的70%以上转化为元素硫,而Au的浸取率则小于3%表明FeCl_3溶液浸取是含Au复杂硫化精矿预处理并回收有价金属的有潜力的方法     

电场作用下浸堆中氧气气体的渗流性质

针对电场作用对堆浸过程中氧气气体在浸堆中传输的影响，在实验室采用三轴渗流实验装置和电场实施装置，研究外加电场作用下浸堆中氧气气体的渗流性质。结果表明：电场作用对浸堆中氧气渗流性质的影响非常明显；电场作用下，氧气气体渗流速度比无电场时要大，并且渗流速度随氧气气体压力梯度增大成线性增加；加电场后，浸堆中氧气气体渗流量随电压（电场强度）升高成线性增大；渗透率越好的浸堆，氧气气体在浸堆中的电动效应越明显。     

地浸工艺与传统采矿法的联合应用

阐述了地下采矿的溶浸工艺 (简称地浸工艺 )与传统工艺在国外的联合应用状况。指出该联合工艺对降低采矿损失贫化的必要性和改进的具体途径。分析研究了开采复杂矿体的新工艺 ,并取得了在矿井条件下直接获取成品的具体经验。这些均为我国采矿工艺的更新和发展提供了依据。