利福平废水的絮凝和生化处理研究

种福平生产的废水ＣＯＤ高达６万,用ＰＦＳ、Ｃ－ＰＡＭ脱稳,密集网捕式絮凝处理后,ＣＯＤ去除率达２７％,ＢＯＤ５／ＣＯＤｃｒ从０．１９上升到０．３２,絮凝前后水质和色谱分析表明,絮凝后５种有机物去除效率均在２２％以上,使生化处理成为可能,进生化池废水经稀释后,用活性污泥法处理９天后,ＣＯＤ从１．５万降至ＣＯＤ〈３００ｍｇ／Ｌ,达到治理要求。     

絮凝—酸化法预处理腈纶纺丝生产废水的实验研究

研究采用絮凝－酸化法对腈纶纺丝废水进行预处理,考察了絮凝剂的选用及多种絮凝实验条件对实验结果的影响。结果表明,以ＰＦＳ作絮凝剂,絮凝ｐＨ６．０,ＰＦＳ 投加量为０．３ｍｌ,ＰＡＭ投加量为０．４ｍｌ时的ＣＯＤ,ＢＯＤ５和ＮＨ３－Ｎ及ＣＮ＾－去除率分别为３０％,３１％,８％及３２％。     

Fe^2＋—H2O2氧化法处理氨基J酸工业废水的研究

用Ｆｅ＾２＋－Ｈ２Ｏ２氧化法处理氨基Ｊ酸工业废水。结果表明,当溶液ｐＨ＝１－３,Ｈ２Ｏ２和Ｆｅ＾２＋用量分别为Ｈ２Ｏ２：Ｆｅ＾２＋１０：１,Ｈ２Ｏ２：ＣＯＤＣｒ＝２ｇ：ｇ时,Ｊ酸废水的ＣＯＤＣｒ去除率达６６．７％,氨基去除率达６８．４％。处理后的废水ＢＯＤ５／ＣＯＤＣｒ＝０．５,已达到生化处理的要求。该法可作为氨基Ｊ酸废水的预处理方法。     

载银TiO2半导体催化剂对印染废水的光降解研究

以新型载银ＴｉＯ２为催化剂，采用高压汞灯为光源对实际印染废水进行了光催化降解的研究。研究结果表明，用新型载银催化剂（简称ＴＳＡ）对印染废水和精炼废水进行深度处理的效果比用ＴｉＯ２为好。在光照１２０分钟条件下，用ＴＳＡ催化剂对印染和精炼废水生化处理出水进行光催化降解，废水的ＣＯＤｃｒ去除率分别达到７５．３％和８３．４％，比同样光降解条件下用单一ＴｉＯ２催化剂时废水的ＣＯＤｃｒ去除率提高２２．９％和２     

活性硅酸混凝剂PFASSC处理造纸废水

利用硅酸钠、硫酸铝、三氯化铁和硫酸为主要原料制备了复合型活性硅酸混凝剂ＰＦＡＳＳＣ并对造纸废水进行了处理，得到活性硅酸混凝剂ＰＦＡＳＳＣ最佳配方为：ＰＨ＝２．０（Ｆｅ＾３＋＋Ａｌ＾２）／ＳｉＯ２（摩尔比）＝１．５，Ｆｅ＾３＋／Ａｌ＾３＋（摩尔比）＝１．０，与常用混凝剂相比，ＰＦＡＳＳＣ混凝剂处理造纸废水对除浊、脱色和去除ＣＤＤＣｒ有更加优良的性能。     

新型无机高分子絮凝剂在制革废水处理中的应用研究

介绍了一种新型无机高分子絮凝剂－硅钙复合型聚合氯化铝铁（ＳＣＰＡＦＣ）在制革废水处理中的应用。结果表明，该产品对废水的浊度去除率为９９％，ＳＳ去除率为９５％，ＣＯＤ去除率为９０％，Ｃｒ＾３＋的去除率为８５％左右。最佳使用ｐＨ值为６．０￣９．０，最佳投药量为０．３５￣０．４０ｇ／Ｌ，最佳混凝时间为１５￣２０ｍｉｎ，在同样条件下各项性能均优于ＰＡＣ２倍以上。同时该絮凝剂还可用于生活饮水、生产用水及其他     

光催化氧化-混凝工艺处理化工废水

探索了光催化氧化－混凝工艺处理废水的工艺条件,最佳光催化氧化处理条件为ＰＨ＝３,催化剂为铁盐,氧化剂Ｈ２Ｏ２,低压汞灯,光照时间１．５ｈ,废水温度４５℃,温凝剂选用ＰＡＣ和ＰＡＭ（混凝剂的投加量为原水ＣＯＤｃｒ：ＰＡＣ：ＰＡＭ＝７：１．５：０．０１）,混凝ＰＨ６,沉降时间０．５ｈ,在该工艺条件对ＣＯＤｃｒ为１７３－７０１４４ｍｇ／Ｌ的十二烷基苯磺酸钠废水、苯酐废水、富马酸废水、邻苯二甲酸二辛酯废水     

生化法处理煤气废水

采用Ａ／Ｏ工艺处理煤气废水的研究结果表明,该工艺能同时去除煤气废水中的有机物和氨氮,在试验确定的条件下,该工艺对煤气废水中的ＣＯＤｃｒ去除率达９１．０％,ＢＯＤ５去除率达９９．１％,ＮＨ３－Ｎ去除率达９９．２％,ＴＮ去除率达９４．７％。     

SBR法处理化学药物制剂废水

采用 ＳＨＲ法处理化学药物制剂废水． 调节 ｐＨ至７．５,进水 ＣＯＤｃｒ ２２４～１５３０ ｍｍ／Ｌ,曝气１０ ｈ, ＣＯＤｃｒ容积负荷达２．５８ｋｇ／ｍ~３·ｄ,ＣＯＤｃｒ的去除率高达９４．２％,处理后出水ＣＯＤｃｒ＜１００ｍｇ／Ｌ,达到综合排放标准（ＧＢ８９７－９６）一级标准。ＣＯＤｃｒ容积负荷至３．８４ ｋｇ／ｍ~３·ｄ, ＣＯＤｃｒ去除率仍＞８５．９％。     

含氟废水的混凝沉淀处理

研究了ＦｅＣｌ３,Ａｌ２（ＳＯ４）３,ＰＦＣＳ和ＡＰＡＭ对含氟废水的混凝沉淀处理。结果表明：石灰乳,ＰＦＣＳ和ＡＰＡＭ对废水中的氟及ＣＯＤ具有较好的处理效果,处理后水质达到国家二级排放标准。     

Color and COD removal from wastewater containing Reactive Black 5 using Fenton's oxidation process

In this study, Reactive Black 5 (RB5) was removed from synthetic wastewater using Fenton's oxidation (FO) process. Experiments were conducted on the samples containing 100 and 200 mg l(-1) of RB5 to remove the dye toxicity. Seventy-five milligram per litre of RB5 caused 25% toxicity on 24-h born daphnids whereas 100 mg l(-1) of RB5 displayed 100% toxicity on Daphnia magna. The study was performed in a systematic approach searching optimum values of FeSO(4) and H(2)O(2) concentrations, pH and temperature. Optimum pH and temperature for 100 mg l(-1) of RB5 were observed as 3.0 and 40 degrees C, respectively, using 100 mg l(-1) of FeSO(4) and 400 mg l(-1) of H(2)O(2) resulted in 71% chemical oxygen demand (COD) and 99% color removal. For 200 mg l(-1) of RB5, 84% COD removal was obtained using 225 mg l(-1) of FeSO(4) and 1000 mg l(-1) of H(2)O(2) yielding 0.05 molar ratio at pH 3.0 and 40 degrees C. Color removal was also more than 99%. The optimum conditions determined in accordance with the literature data. The H(2)O(2) requirement seems to be related to initial COD of the sample. FeSO(4)/H(2)O(2) ratios found were not changed for both concentrations. The temperature affected the COD removal significantly at high degrees. Toxicity was completely removed for each concentration of RB5 at optimum removal conditions.     

混凝-Fenton氧化-Fe0还原预处理高浓度硝基苯生产废水

采用混凝-Fenton氧化-Fe0还原工艺预处理高浓度硝基苯废水,考察各反应阶段硝基苯去除效果及影响因素。研究表明,聚铁混凝性能优于聚铝;初始COD为17 350 mg/L、硝基苯浓度为10 050 mg/L的废水,在pH=4,聚铁投加浓度3 300 mg/L时,COD和硝基苯去除率分别为63%和62%;混凝沉降后的上清液用Fenton试剂氧化,可在较宽pH(3～6)范围内降解硝基苯,当H2O2(30%)浓度为6 000 mg/L,Fe2+浓度为168 mg/L时,氧化效率最高;聚铁混凝-Fenton氧化后的出水用Fe0还原,最佳还原条件为:pH=3,Fe0浓度1 500 mg/L。原水经聚铁混凝-Fenton氧化-Fe0还原后,COD和硝基苯总去除率分别达90%和98%,总药剂成本约12.4元/t。处理后废水硝基苯浓度为168 mg/L,适宜进行后续的厌氧-好氧生物处理。     

强化UV/Fenton法降解水中苯酚的研究

研究了UV/Fenton法处理含苯酚废水时H2 O2 和FeSO4 加入量及苯酚初始浓度对酚去除效果的影响及C2 O2 -4 对UV/Fenton法的增强效果。 [H2 O2 ]=2 0mmol/L ,[FeSO4 ]=5mmol/L ,反应 2 0min ,苯酚初始浓度为 5 0mg/L时 ,酚去除率达 99%。UV/Fenton体系中引入C2 O2 -4 后可有效提高对紫外和可见光的利用率 ,进而提高了对高浓度苯酚废水去除效果     

光催化氧化深度处理电镀有机废水的工程化实验

采用光催化氧化联用技术对电镀有机废水进行深度处理工程化实验。探讨了uV、uV＋H2O3、uV＋H2O2＋TiO2、uV＋H2O2＋FeSO4、uV＋H2O2＋FeSO4＋TiO2、uV＋O3＋TiO2和uV＋03＋TiO2＋H2O2等体系对废水有机污染物去除率的影响。结果表明,相较于其他反应体系,uV＋O3＋TiO2＋H2O2体系具有更好的氧化效果,经碳滤处理后去除率达到90％以上,最终出水水质满足GB18918-20O2-级标准（A标准）的要求。实际运行项目偿还期5．33年,NPV〉0,内部收益率大于基准值10％。研究表明,uV＋O3＋TiO2＋H2O,体系能降低加药量,工作量及运行成本。可为电镀企业实际废水处理提供现实依据,为优化电镀废水的处理工艺提供参考。     

混凝法处理含铜电镀废水的实验研究

以FeSO₄、PAC作为絮凝剂去除低浓度电镀废水中的Cu^{2+,考察了絮凝剂投加量、溶液pH值、搅拌速度和时间等影响因素,结果表明,在各自最佳条件下,PAC和FeSO₄对Cu2+的去除可达到99.37%和99.20％,达到《污水综合排放标准》(GB 8978-1996)中一级排放标准。最后通过对FeSO₄、PAC和NaOH 3种药剂的综合分析和比较,发现FeSO₄絮凝处理低浓度电镀废水中的铜比PAC絮凝、NaOH沉淀法操作简单,污泥产生量少、工业应用性强而且去除率高。}     

Fenton/絮凝工艺深度处理制浆造纸废水的工程应用分析

以某制浆造纸厂生化出水Fenton/絮凝深度处理工艺长期运行数据为依据,系统分析了H2O2、废酸液（FeSO4含量约8%）、硫酸铝、PAM及氧化钙等处理药剂用量与水量、进水负荷和COD去除量之间的关系。结果表明,H2O2、废酸液、硫酸铝、PAM及氧化钙的单位水量平均投加量分别为0.05、2.18、0.07、0.0075和0.27 kg/m3,而去除单位COD的药剂平均消耗量分别为0.20、8.48、0.27、0.029和1.06 kg/（kg COD）;H2O2、废酸液、硫酸铝和氧化钙的用量随进水负荷的增大而增加,而PAM随进水负荷的变化较小。H2O2和FeSO4的投加摩尔比（MH2O2/Fe2＋）主要集中在1.0-2.0之间,其中在1.0-1.6之间的累积频率达到93%。该工艺的出水COD和SS分别为65-100 mg/L和20-30 mg/L,达到《制浆造纸工业水污染物排放标准》（GB 3544-2008）排放要求。废水深度处理成本约为1.01元/m3,其中药剂费用约0.58元/m3,占56.98%。     

Removal of heavy metals from anaerobically digested sewage sludge by isolated indigenous iron-oxidizing bacteria

The removal of heavy metals (Cr, Cu, Zn, Ni and Pb) from anaerobically digested sludge from the Yuen Long wastewater treatment plant, Hong Kong, has been studied in a batch system using isolated indigenous iron-oxidizing bacteria. The inoculation of indigenous iron-oxidizing bacteria and the addition of FeSO4 accelerated the solubilization of Cr, Cu, Zn, Ni and Pb from the sludge. pH of the sludge decreased with an increase in Fe2+ concentrations and reached a low pH of 2-2.5 for treatments receiving both bacterial inoculation and FeSO4. After 16 days of bioleaching, the following heavy metal removal efficiencies were obtained: Cr 55.3%, Cu 91.5%, Zn 83.3%, Ni 54.4%, and Pb 16.2%. In contrast, only 2.6% of Cr, 42.9% of Cu, 72.1% of Zn, 22.8% of Ni and 0.56% of Pb were extracted from the control without the bacterial inoculation and addition of FeSO4. The residual heavy metal content in the leached sludge was acceptable for unrestricted use for agriculture. The experimental results confirmed the effectiveness of using the isolated iron-oxidizing bacteria for the removal of heavy metals from sewage sludge.     

水处理中含铁废料综合利用的研究进展

回顾了２０余年来我国在水处理中综合利用含铁废料的研究进展，分别评述了副产品硫酸亚铁制备絮凝剂ＰＦＳ的各种方法，废铁屑运用于内电解法水处理和其他含铁泥渣，废酸在水处理中的研究和应用现状，指出含铁废料综合利用中有待于进一步研究的若干问题。     

Bacterial leaching of heavy metals from sewage sludge-bioreactors comparison

More than 50% of municipal sewage sludges cannot be used on agricultural land because of their heavy metals content. Therefore, microbial leaching of heavy metal from municipal sludge was studied in a continuously stirred tank reactor without recycling (CSTR) or with sludge recycling (CSTRWR) at residence times of 1, 2, 3 and 4 days. The reactor CSTRWR is supposed to be more efficient for bacterial process due to the recycling of active bacteria from the settling tank to the reactor. The CSTRWR and the CSTR with 1 g litre(-1) FeSO(4).7H(2)O addition were equally efficient because of copper reprecipitation or recomplexation in the settling tank of the CSTRWR. In the CSTR, about 62% of copper and about 77% of zinc were dissolved in 3 days residence time compared to 50% of copper and 64% of zinc in the CSTRWR, if 3 g litre(-1) FeSO(4).7H(2)O was added. Thus with larger amount of substrate, the CSTR was more efficient than the CSTRWR. Residence time and pH were the main factors for zinc solubilization while for copper, the redox potential was also a major factor. The effect of FeSO(4).7H(2)O concentration on bacterial activity to solubilize heavy metals was also studied, increased concentration of FeSO(4).7H(2)O yielded better copper solubilization while it had no effect or a negative effect on zinc. This supports the hypothesis of a direct mechanism for zinc solubilization and of an indirect mechanism for copper solubilization.     

Comparison of various advanced oxidation processes and chemical treatment methods for COD and color removal from a polyester and acetate fiber dyeing effluent

In this paper, a comparison of various advanced oxidation processes (O3, O3/UV, H2O2/UV, O3/H2O2/UV, Fe2+/H2O2) and chemical treatment methods using Al2(SO4)3.18H2O, FeCl3 and FeSO4 for the chemical oxygen demand (COD) and color removal from a polyester and acetate fiber dyeing effluent is undertaken. Advanced oxidation processes (AOPs) showed a superior performance compared to conventional chemical treatment, which maximum achievable color and COD removal for the textile effluent used in this study was 50% and 60%, respectively. Although O3/H2O2/UV combination among other AOPs methods studied in this paper was found to give the best result (99% removal for COD and 96% removal for color), use of Fe2+/H2O2 seems to show a satisfactory COD and color removal performance and to be economically more viable choice for the acetate and polyester fiber dyeing effluent on the basis of 90% removal.