Decomplexation of Cu-1-hydroxyethylidene-1,1-diphosphonic acid by a three-dimensional electrolysis system with activated biochar as particle electrodes

The feasibility of decomplexation removal of typical contaminants in electroplating wastewater, complexed Cu(II) with 1-hydroxyethylidene-1,1-diphosphonic acid (Cu-HEDP), was first performed by a three-dimensional electric reactor with activated biochar as particle electrodes. For the case of 50 mg/L Cu-HEDP, Cu(II) removal (90.7%) and PO initial pH 7, acid-treated almond shell biochar (AASB) addition 20 g/L, and reaction time 180 min, with second-order rate constants of 1.10 × 10⁻³ and 1.94 × 10⁻⁵ min⁻¹respectively. The growing chelating effect between Cu(II) and HEDP and the comprehensive actions of adsorptive accumulation, direct and indirect oxidation given by particle electrodes accounted for the enhanced removal of Cu-HEDP, even though the mineralization of HEDP was mainly dependent on anode oxidation. The performance attenuation of AASB particle electrodes was ascribed to the excessive consumption of oxygen-containing functionalities during the reaction, especially acidic carboxylic groups and quinones on particle electrodes, which decreased from 446.74 to 291.48 µmol/g, and 377.55 to 247.71 µmol/g, respectively. Based on the determination of adsorption behavior and indirect electrochemical oxidation mediated by in situ electrogenerated H₂O₂ and reactive oxygen species (e.g., •OH), a possible removal mechanism of Cu-HEDP by three-dimensional electrolysis was further proposed.     

生物氧化塔的应用

介绍了生物氧化培处理含油污水的装置运行情况．大量数据说明该塔具有操作弹性大，适用范围广，能耗低，脱除率高，不外排过剩的活性污泥等特点，具有广阔的推广应用前景。     

Mn-Cu-O负载型催化剂上CO氧化性能的研究

研究了ＺｒＯ２或Ａｌ２Ｏ３负载Ｍｎ－Ｃｕ－Ｏ体系催化剂ＣＯ催化氧化活性，以及物相结构，表面氧性能与活性的关系。结果表明，锆基催化剂的氧化活性明显优于铝基催化剂，起燃温度Ｔ５０低达５０℃，ＺｒＯ２载 利于活性组份形成高活性物相，并促进表面吸附氧的脱附，表现出催化剂表面吸附氧的脱附温度高低次序与其氧化活性有一致的对应关系。     

混凝沉淀-水解酸化-生物吸附-UBF-接触氧化一氧化沟-吸附工艺处理聚醚多元醇废水

对聚醚多元醇废水采用混凝沉淀-水解酸化-生物吸附-UBF-接触氧化一氧化沟-吸附等进行连续处理。结果表明，该处理工艺具有废水处理效果好、出水水质稳定（出水水质达GB8978—1996中的一级标准）、操作管理方便等优点，是处理该类化工废水的有效方法之一。     

Fe3+催化氧化S(Ⅳ)反应机理初探

通过分析酸性条件下(pH为1～3),Fe3 催化氧化S(Ⅳ)过程中溶液吸光度变化的趋势,对Fe3 催化氧化S(Ⅳ)的反应机理进行了初步推导.实验证明,液相中该反应机理主要是催化氧化与自由基反应相结合,O2的存在对于反应有重要作用,O-2的生成是S(Ⅳ)被氧化的关键;当水中溶解氧接近耗尽时,反应进程发生改变.当Fe3 、S(Ⅳ)浓度增加,自由基生成量增加时,有利于反应进行;作为反应产物,Fe2 、S(Ⅵ)浓度增加,反应推动力减小,反应速率降低;同时Fe2 、SO24-可以与溶液中的其它物质形成配合物,影响了Fe3 -S(Ⅳ)配合物的生成与分解,不利于S(Ⅵ)的氧化.     

胰岛素废水处理工程设计

针对某医药公司在制取胰岛素过程中产生的高浓度废水，采用预处理（酒精回收-盐水投配-除油）-倒A2O-接触氧化-化学除磷组合工艺进行调试，其处理效果明显，出水各项指标均能达标，同时对工艺中存在的缺陷进行了分析。     

Fenton试剂处理青霉素废水实验研究

以青霉素废水为研究对象 ,初步探讨了 Fenton试剂处理有毒有机废水时各影响因素的作用机制 ,通过实验确定了 Fenton试剂氧化降解青霉素废水的适宜操作条件为 :CODCr为 30 0 0 mg/L左右的青霉素废水 ,p H为 6.0、H2 O2 (30 % )投加量为 0 .6% (体积分数 )、Fe SO4 · 7H2 O投加量为 0 .2 % (质量分数 )、反应时间为 lh,此条件下废水 CODcr的去除率可达 70 % ,而且该方法设备简单 ,易于下一步实现工业放大 ,是一种有较好开发前景的处理青霉素废水工艺。     

制革废水的治理

介绍了采用调节—混凝沉淀—生物接触氧化工艺处理制革生产废水工程的设计调试运行结果。从运行效果看该工程因地制宜，投资省，运行费用低，处理效果好，出水可达到排放标准。     

活性炭吸附-光催化氧化深度净水工艺实验研究

以光催化氧化作为活性炭吸附工艺出水通常存在的亚硝酸盐、余氯与细菌总数超标等问题,并能去除铁穿透炭层的极性短链有机污染物,使出水达到《饮用净水水质标准》（CJ94－1999）。与目前常用的活性炭－反渗透组合工艺相比,该工艺具有可保留水中有益的矿物成分的特点,具有良好的应用前景。     

Preparation of PFS coagulant by sectionalized reactor

The oxidation rate of ferrous sulfate is investigated for the preparation of polyferric sulfate(PFS)coagulant.In is proved that this reaction is zero order with respect to Fe^2 ,first order with respect to NO2(g),and first order with respect to the interface area between gas phase and liquid phase.According to this mechanism,sectionalized reactor(SR) is used in place of traditional reactor(TR),and the liquid of reaction mixture is recycled by pump.As a result,not only the flow path of reaction liquid is prolonged,but also gas-liquid contact area enlarged,and the reaction distinctly accelerated,compared with traditional reactor.The effects of parameters including temperature,acidity and others on the reaction rate are also discussed.