中小型制革企业综合废水处理工程的设计与应用

采用载体固体床为主要处理单元，辅以高效混凝剂处理中小型制革综合废水，工程运行表明：在进水CODcr,SS,S^2-，总铬的平均浓度在762mg/L,732mg/L,31mg/L,15mg/L的条件下，排水中的CODcr,SS,S^2-，总铬平均浓度为129mg/L,95mg/L,0.47mg/L,0.8mg/L。处理后的水质达到了GB8978-1996《污水综合排放标准》中的Ⅱ级标准。     

模糊综合评价法在水质变化和水体管理中的应用

应用模糊数学中的模糊综合评价法，对徐州市的地面水体的水质变化趋势进行了探讨，结果表明模糊综合评价法能及时发现水质恶化现象，对水体的管理具有指导作用．     

危险化学品活性反应危害及混配危险的规则研究（XIII）

非金属氢化物具有EHn活性基刚，大多数挥发性氢化物的最低爆炸氰浓度几乎是零。因此，在处理非金属氢化物时，全部除掉空气或氧气对安全操作是重要的。在氢化混合物中有杂质时会更进一步增加着火的危险。值得强调的是：硫化氢不仅与空气混合能形成爆炸性混合物，而遇明火、高热且能引起燃烧或爆炸。     

多元素分析器分析砷遇到的问题与方法改进

依据新银盐分光光度法的基本原理,使用多元素分析器准确测定水体中砷的含量会遇到一些问题,如砷标准使用液浓度,吸收液配制,U型管DMF混合液加入量,脱脂棉装入U型管松紧程度,反应水样酸度,反应/吸收装置的致密性和一致性以及使用玻璃器皿的洗涤等,如果这些操作步骤不当都会给测定结果带来一定的误差,为了尽量减少这些误差,分析者对该项目测定方法作了一些探讨和改进,收到了良好的成效.     

木屑和花生壳吸附去除水溶液中Cr3+的试验研究

以废弃物木屑和花生壳作为吸附剂,进行了吸附去除水中Cr3 的试验.研究了溶液pH值、初始Cr3 浓度以及温度等因素对这2种吸附剂去除Cr3 作用的影响,对吸附曲线作了线性拟合,确定了相应的平衡吸附率,在Cr3 初始浓度为1、5、10和20 mg/L时,木屑对Cr3 的平衡吸附率为81%、68%、56%和40%,花生壳依次为77%、63%、53%和42%,并探讨了这2种吸附剂对溶液中Cr3 的吸附机理.     

基于SWAT模型的泗河流域除草剂迁移模拟

泗河流域农药污染对南四湖湖泊乃至南水北调工程具有重要的影响,为了解流域农药迁移过程并对其采取治理措施,本研究在泗河流域通过实地采样与调查、室内实验分析、数据统计等手段,借助SWAT模型对流域除草剂阿特拉津及其代谢产物进行迁移模拟.结果表明,除草剂输出与流域径流量有很高的相关性,输出时间以7~8月份为主,输出量占全年的69%以上.且受河道长度、耕地分布等因素的影响,阿特拉津的输出量以东部上游地区和中部地区为主,流域出水口处的阿特拉津输出量居中等水平;阿特拉津代谢产物DEA和DIA的输出量的空间分布相似,以下游流域出口处和中部地区为主.本研究可为流域除草剂迁移治理提供理论支持.     

不同类型清水剂处理油田含聚污水的效果对比

考察了阳离子型CWC-14、非离子型NQS-01和阴离子型AQS-08 3类清水剂对油田含聚污水的处理效果,对比了它们的作用特点和絮体性能。实验结果表明:在清水剂加入量350 mg/L、处理温度65℃、搅拌转速300 r/min、搅拌时间5 min的条件下,CWC-14、NQS-01和AQS-08对含聚污水的除油率分别为98.8%、98.0%和99.4%;NQS-01受处理温度、搅拌条件影响较大;CWC-14受污水中聚合物质量浓度影响最大。清水剂的絮体特点与其作用机理有关,CWC-14的絮凝速率最快,起效时间最短,絮体呈黏性大块状;NQS-01的絮凝速率最慢,起效时间最长,絮体呈浮油状;AQS-08的絮凝速率和起效时间适中,絮体呈松散状、流动性好。对比结果表明,非阳离子型清水剂可有效避免油田含聚污水处理过程中的黏性油泥问题。     

Preparation of MgCr<Subscript>2</Subscript>O<Subscript>4</Subscript> from waste tannery solution and effect of sulfate,chloride, and calcium on leachability of chromium

This paper presents a study regarding the preparation of MgCr₂O₄ from waste tannery solution, and chromium leaching behavior is also investigated with varying amounts of sulfate, chloride and calcium. The phase transformation, crystallinity index and crystallite diameter were characterized using XRD, FT-IR and thermal analysis. A well-crystallized MgCr₂O₄ was successfully prepared at 1400 °C. The sintering temperature had a major impact on the formation of MgCr₂O₄ compared with sintering time. The MgCr₂O₄ phase was observed initially at 400 °C and its crystallite diameter increased with increasing temperature. The concentration of total chromium leached and Cr(VI) decreased gradually with increasing temperature. The considerable amount of Cr(VI) was found in the leachate at 300–500 °C caused by Cr(VI) intermediary products. Sulfate and chlorine could impact the transformation efficiency of chromium adversely, and chlorine has a more significant effect than sulfate. The presence of calcium disturbed the formation of MgCr₂O₄ and new chromium species (CaCrO₄) appeared, which resulted in a sharp increase in the concentration of leached Cr(VI). Incorporating Cr(III) into the MgCr₂O₄ spinel for reusable products reduced its mobility significantly. This was demonstrated to be a promising strategy for the disposal of chromium containing waste resource.     

Synthesis of novel CeO2-BiVO4/FAC composites with enhanced visible-light photocatalytic properties

To utilize visible light more effectively in photocatalytic reactions, a fly ash cenosphere （FAC）-supported CeO2-BiV04 （CeO2-BiVO4/FAC） composite photocatalyst was prepared by modified metalorganic decomposition and impregnation methods. The physical and photophysical properties of the composite have been characterized by X-ray diffraction （XRD）, scanning electron microscope （SEM） and energy dispersive X-ray spectroscopy （EDX）, X-ray photoelectron spectroscopy （XPS）, and UV-Visible diffuse reflectance spectra. The XRD patterns exhibited characteristic diffraction peaks of both BiVO4 and Ce02 crystalline phases. The XPS results showed that Ce was present as both Ce4＋ and Ce3＋ oxidation states in Ce02 and dispersed on the surface of BiV04 to constitute a p-n heterojunction composite. The absorption threshold of the CeO2-BiVO4/FAC composite shifted to a longer wavelength in the UV-Vis absorption spectrum compared to the pure Ce02 and pure BiV04. The composites exhibited enhanced photocatalytic activity for Methylene Blue （MB） degradation under visible light irradiation. It was found that the 7.5 wt.% CeO2-BiVO4/FAC composite showed the highest photocatalytic activity for MB dye wastewater treatment.     

Cosolvent-enhanced chemical oxidation of perchloroethylene by potassium permanganate

A laboratory study was conducted to examine cosolvent-enhanced in-situ chemical oxidation (ISCO) of perchloroethylene (PCE) using potassium permanganate (KMnO4). The conceptual basis for this new technique is to enhance permanganate oxidation of dense non-aqueous phase liquids (DNAPLs) with the addition of a cosolvent, thereby increasing DNAPL solubility while avoiding mobilization. Among 17 cosolvent candidates screened, tertiary butyl alcohol (TBA) and acetone were the most stable in the presence of KMnO4, both of which increased PCE aqueous solubility significantly, and therefore are suitable to be used as cosolvent in this study. Batch experiments indicated that the second-order rate constant for PCE oxidation by potassium permanganate was 0.043+/-0.002 M(-1) s(-1) in the purely aqueous (no cosolvent) solution. In the presence of 20% cosolvent (volume fraction=fc=0.2), the rate constant decreased to 0.036+/-0.003 M(-1) s(-1) with TBA and to 0.031+/-0.002 M(-1) s(-1) with acetone. However, in the presence of free-phase PCE, chloride ion concentration from PCE oxidation in acetone/water solutions (fc=0.2) was about twice that in aqueous solutions, indicating that the increase in PCE solubility more than compensated for the decrease in reaction rate constant, such that the oxidation efficiency of PCE was increased with cosolvent. A complete chlorine mass balance was observed in the aqueous system, whereas approximately 70% was obtained in TBA/water or acetone/water (fc=0.2). In soil columns containing residual DNAPL and subjected to isocratic flushing with step-wise increases in f(c) cosolvent, TBA at fc=0.2 resulted in PCE mobilization, whereas acetone at fc相似文献