转炉渣诱导磷酸钙结晶法去除和回收废水中磷的研究

以转炉渣为晶种材料,利用批次结晶沉淀实验,研究不同的反应条件对诱导磷酸钙结晶法去除和回收废水中磷的影响。结果表明,最优反应条件为:pH=9.5,Ca/P摩尔比2∶1,转炉渣用量1.7 g/L,反应时间3 h,在此条件下,碳酸根对反应的影响甚小,对养猪场废水和污泥浓缩池上清液的处理,最高去除率分别达到95.36%和96.54%;转炉渣循环利用10次,回收磷的效果仍然很好。运用扫描电子显微镜(SEM)、X射线能谱仪(EDS)和X射线衍射仪(XRD)等测试手段对在最优工艺条件下重复使用10次的转炉渣进行了表征,证明回收的磷主要以羟基磷灰石(HAP)形态存在。     

立式磨和袋式除尘器在矿渣粉磨系统中的应用

阐述了矿渣微粉的应用、粉磨工艺和设备现状,并对立式磨生产工艺、立式磨结构和工作原理、袋式除尘器结构和工作原理等进行了重点介绍,分析了工程应用实例,认为国产立式磨和袋式除尘器可为矿渣粉磨的节能减排提供可靠的技术和设备保障。     

面向矿山废弃地复垦的炉渣污泥人工土壤的理化特性

通过添加不同比例的燃煤电厂粉煤灰和炉渣对城市污泥进行钝化,配制成不同灰渣比例的人工土壤,对人工土壤的pH、电导率、养分含量、重金属含量以及持水、渗水性能进行了研究。结果表明,污泥人工土壤pH介于7.5～8.0之间,属于弱碱性土壤;电导率变化范围为2.93～3.71 mS/cm,表明盐分含量较高。污泥人工土壤中有效态养分含量随炉渣比例提高而增加,所有配比人工土壤有机质和有效磷、速效钾的含量达到高肥力水平。人工土壤中Cd、Ni、Pb、Cu、Zn含量均明显低于国家农用标准(GB 4284-84、GB 8173-87)。粉煤灰渣对污泥中有效态Cd、Ni、Pb和Cu有钝化作用,使其向无效态转化,对Zn则有活化作用。炉渣对Cd、Ni的钝化作用要优于粉煤灰,而粉煤灰对Pb、Cu的钝化作用要优于炉渣。添加炉渣提高了污泥人工土壤水分的蒸发量,减弱了人工土壤的持水能力,但加入炉渣使人工土壤的渗透系数显著增加,提高了其渗水性能。     

Preparation of glass-ceramics from molten steel slag using liquid-liquid mixing method

A novel approach to prepare glass-ceramics from molten steel slag (MSS) was proposed. In laboratory, the water-quenched steel slag was melted at 1350 °C to simulate the MSS. A mixture of additive powders in wt.% (55 quartz powder, 5 Na₂O, 16 emery powder, 15 CaO, 8 MgO, 1 TiO₂) were melted into liquid at 1350 °C separately. Then the MSS and the molten additives were mixed homogeneously in order to obtain parent glass melt. The proportion of MSS in the melt was 50 wt.%. The melt was subsequently cast, annealed, heat-treated and transformed into glass-ceramics. Their microstructure and crystallization behavior were analyzed. The samples exhibited excellent properties and displayed bulk crystallization. The major crystallized phase was diopside ((Fe_0.35Al_0.20Mg_0.44)Ca_0.96(Fe_0.08Si_0.70Al_0.20)₂O_6.12), which was uniformly distributed in the microstructure. The novel approach may help iron and steel industry achieve zero disposal of steel slag with utilization of the heat energy of the MSS.     

Changes in mineralogical and leaching properties of converter steel slag resulting from accelerated carbonation at low CO2 pressure

Steel slag can be applied as substitute for natural aggregates in construction applications. The material imposes a high pH (typically 12.5) and low redox potential (Eh), which may lead to environmental problems in specific application scenarios. The aim of this study is to investigate the potential of accelerated steel slag carbonation, at relatively low pCO₂ pressure (0.2 bar), to improve the environmental pH and the leaching properties of steel slag, with specific focus on the leaching of vanadium. Carbonation experiments are performed in laboratory columns with steel slag under water-saturated and -unsaturated conditions and temperatures between 5 and 90 °C. Two types of steel slag are tested; free lime containing (K3) slag and K1 slag with a very low free lime content. The fresh and carbonated slag samples are investigated using a combination of leaching experiments, geochemical modelling of leaching mechanisms and microscopic/mineralogical analysis, in order to identify the major processes that control the slag pH and resulting V leaching. The major changes in the amount of sequestered CO₂ and the resulting pH reduction occurred within 24 h, the free lime containing slag (K3-slag) being more prone to carbonation than the slag with lower free lime content (K1-slag). While carbonation at these conditions was found to occur predominantly at the surface of the slag grains, the formation of cracks was observed in carbonated K3 slag, suggesting that free lime in the interior of slag grains had also reacted. The pH of the K3 slag (originally pH ± 12.5) was reduced by about 1.5 units, while the K1 slag showed a smaller decrease in pH from about 11.7 to 11.1. However, the pH reduction after carbonation of the K3 slag was observed to lead to an increased V-leaching. Vanadium leaching from the K1 slag resulted in levels above the limit values of the Dutch Soil Quality Decree, for both the untreated and carbonated slag. V-leaching from the carbonated K3 slag remained below these limit values at the relatively high pH that remained after carbonation. The V-bearing di-Ca silicate (C2S) phase has been identified as the major source of the V-leaching. It is shown that the dissolution of this mineral is limited in fresh steel slag, but strongly enhanced by carbonation, which causes the observed enhanced release of V from the K3 slag. The obtained insights in the mineral transformation reactions and their effect on pH and V-leaching provide guidance for further improvement of an accelerated carbonation technology.     

铬渣无害化处理技术研究进展

综述了铬渣无害化处理技术的研究进展,分析了各种技术在实际应用过程中的效果,指出各种处理技术的优缺点,详细介绍了固化法中水泥固化和药剂稳定化两种处理技术,提出开发重金属螯合剂是今后铬渣稳定化处理的研究方向.     

含砷冶炼废渣高温烧结过程砷的迁移特性

研究了烧结温度和烧结时间对含砷冶炼废渣烧结过程中砷的迁移特性的影响。烧结条件为在10 MPa下加压成型,进空气流量为2 000 mL/min,烧结温度1 000～1 350℃,烧结时间5～120 min。结果表明,烧结过程中存在砷的挥发,但烧结前后砷的总量变化不大,砷的固化率均保持在90%以上。毒性浸出实验表明,不同的烧结条件对烧结体中砷的毒性浸出有重要的影响,从烧结体的环境安全性考虑,最佳的烧结温度和时间分别为1 200℃和45 min。     

高炉渣制备聚硅酸硫酸铝铁混凝剂

以高炉渣为原料,分别采用酸浸及碱浸-酸化工艺得到铁、铝离子及聚硅酸,再将铁、铝离子引入聚硅酸制得聚硅酸硫酸铝铁(PSAFS)混凝剂。考察了PSAFS的聚合条件对焦化废水混凝效果的影响,并与市售混凝剂进行了对比。实验结果表明:PSAFS的最佳制备条件为n(Al+Fe)∶n(Si)=0.53,混凝剂p H=1,熟化时间0.5 h,熟化温度60℃;PSAFS加入量为4 m L/L时,混凝效果最好,对焦化废水的浊度和COD的去除率分别达到98.9%和74.5%;PSAFS的性能优于市售的3种混凝剂。     

Remediation of Cr(VI) from chromium slag by biocementation

Here we demonstrate a calcifying ureolytic bacterium Bacillus sp. CS8 for the bioremediation of chromate (Cr(VI)) from chromium slag based on microbially induced calcite precipitation (MICP). A consolidated structure like bricks was prepared from chromium slags using bacterial cells, and five stage Cr(VI) sequential extraction was carried out to know their distribution pattern. Cr(VI) mobility was found to significantly be decreased in the exchangeable fraction of Cr slag and subsequently, the Cr(VI) concentration was markedly increased in carbonated fraction after bioremediation. It was found that such Cr slag bricks developed high compressive strength with low permeability. Further, leaching behavior of Cr(VI) in the Cr slag was studied by column tests and remarkable decrease in Cr(VI) concentration was noticed after bioremediation. Cr slags from columns were characterized by SEM–EDS confirming MICP process in bioremediation. The incorporation of Cr(VI) into the calcite surface forms a strong complex that leads to obstruction in Cr(VI) release into the environment. As China is facing chromium slag accidents at the regular time intervals, the technology discussed in the present study promises to provide effective and economical treatment of such sites across the country, however, it can be used globally.