柱后衍生离子色谱法测定土壤和沉积物中的六价铬

采用加热回流提取、柱后衍生离子色谱法分离土壤和沉积物中的六价铬,使用紫外可见检测器进行测定。选用7种土壤和沉积物的实际样品,依次讨论了氢氧化钠-碳酸钠溶液、碳酸氢钠溶液、氢氧化钠-氯化钾溶液、离子色谱碱性淋洗液4种不同提取剂对六价铬的提取效率,以及超声提取、水浴振荡提取和恒温磁力搅拌冷凝回流3种提取方式的提取效果;研究了10～60 min、25～190℃条件下的最佳提取时间和加热温度;分析了不同提取剂体积和称样量比值条件下六价铬标土的测定量,并探究了提取液的保存条件。优化后的前处理条件：称取2.5 g筛分后的土壤或沉积物样品,加入25 mL NaOH/Na₂CO₃提取剂,在恒温磁力搅拌冷凝回流装置上于120℃加热回流60 min,离心后用0.22μm滤膜过滤,用柱后衍生离子色谱紫外检测装置进行测定。相比目前常用的分光光度法、原子吸收法等测定土壤中六价铬方法,柱后衍生离子色谱法特异性强,降低了差减法或其他前处理技术测定六价铬时所引入的误差,且不受提取液色度、浊度等影响。方法检出限可达0.002 mg/kg,灵敏度高,操作简便,抗干扰能力强,对于...     

接触氧化法深度去除二级出水中氨氮的研究

采用生物接触氧化法对生活污水处理厂出水进行深度处理,探讨了水力停留时间、温度及pH值等因素对氨氮去除效果的影响。结果表明：水力停留时间1．5h时,污水厂出水经过处理后氨氮的浓度小于5mg／L,去除率达到82％以上,出水符合国家生活杂用水水质标准(CJ25,1-89)。     

新型絮凝剂用于草浆造纸废水处理研究

用一种先经改性后的高分子化合物合成一种新型的絮凝剂WD 1型。应用这种絮凝剂分别处理用稻草和麦杆制浆的造纸废水。废水经一次絮凝,COD可由大于2000mg/L,除至300mg/L以下,取得满意的结果。研究了絮凝剂的用量、温度、废水的pH、陈放时间等对去除废水中COD的影响。     

纳滤膜处理炼油厂循环冷却水排水

采用高效混凝沉降—超滤工艺对循环冷却水排水进行预处理后,考察了NF-A、NF-B和NF-C型纳滤膜的运行情况和处理效果.实验结果表明:NF-A膜对COD、Ca2+和Mg2+的去除率均较低,对Clˉ没有去除效果;NF-C膜对COD、Ca2+、Mg2+和SO42-的去除率均较高,对Clˉ去除率为83.1％,但运行压力较高;NF-B膜运行压力居中,对COD去除率为95.9％,对Ca2+去除率为98.3％,对Mg2+去除率为93.4％,对SO42-去除率为98.2％,对Clˉ去除率为67.4％,处理后出水达到循环回用的要求.     

Advanced oxidation treatment of pulp mill effluent for TOC and toxicity removals

Pulp mill effluent was treated by different advanced oxidation processes (AOPs) consisting of UV, UV/H2O2, TiO2-assisted photo-catalysis (UV/TiO2) and UV/H2O2/TiO2 in lab-scale reactors for total organic carbon (TOC) and toxicity removals. Effects of some operating parameters such as the initial pH, oxidant and catalyst concentrations on TOC and toxicity removals were investigated. Almost every method resulted in some degree of TOC and toxicity removal from the pulp mill effluent. However, the TiO2-assisted photo-catalysis (UV/TiO2) resulted in the highest TOC and toxicity removals under alkaline conditions when compared with the other AOPs tested. Approximately, 79.6% TOC and 94% toxicity removals were obtained by the TiO2-assisted photo-catalysis (UV/TiO2) with a titanium dioxide concentration of 0.75gl(-1) at pH 11 within 60min.     

催化臭氧氧化对生化尾水中典型有机物的去除特性

系统深入地分析了Fe-Ce/AC催化臭氧氧化对化工园区污水厂生化尾水中典型有机物的去除特性。与单独臭氧氧化相比,催化臭氧氧化可将TOC去除率从7.89%大幅提升至17.54%。120 min时UV_(254)和特征紫外吸光度(SUVA)的去除率分别高达66.80%和59.73%,证明了催化臭氧氧化可有效去除含共轭结构或芳环结构的不饱和有机物。催化臭氧氧化对生化尾水中腐殖酸类(HA)、溶解性微生物产物类(SMP)和疏水性腐殖酸类(HOA)3种荧光组分的去除过程均符合一级动力学模型,且由一级动力学速率常数可知,与生化尾水色度直接相关的HA和HOA被优先去除。40 min时HA、SMP和HOA的去除率即高达95.24%、93.21%和92.96%。     

印染废水生化出水中各类有机物在Fenton 氧化过程中的去除效果

考察了Fenton氧化法处理印染废水生化出水时,不同因素对色度去除效果的影响。在最佳处理条件下,即[H2O2]∶[Fe2＋]为6∶1,反应初始pH为4.0,H2O2和FeSO4的投加量分别为3.6 mmol/L和0.6 mmol/L,反应时间为30min,UV254、DOC和COD的去除率分别达到了84%、52%和84%,ADMI7.6和稀释倍数表征的色度去除率分别达到了94%和96%。通过XAD-8/XAD-4吸附树脂联用技术将印染废水生化出水中溶解性有机物分为疏水酸、非酸疏水物质、弱疏水物质及亲水物质4类有机物。实验结果表明,对于该印染废水的生化出水,疏水性物质是引起色度的主要物质,所占比例以ADMI7.6表征时为92%,其中以非酸疏水物质的贡献最大,达到53%。Fenton试剂氧化处理对此水样中的非酸疏水物质和疏水酸均有较好的去除效果,对弱疏水性有机物和亲水性有机物去除率较低。     

造纸白泥和粉煤灰的添加对污泥消化液中氮磷回收的影响

污泥厌氧消化液中含有丰富的氮磷,若直接排放到环境中,将会对附近水体造成严重污染。由于消化液中Mg^2＋和Ca^2＋的含量很低,严重影响了氮磷的回收效果。把造纸白泥和粉煤灰引入到污泥厌氧消化液氮磷的回收当中,可以明显地提升消化液pH和提高PO4^3-P和NH3-N回收率。实验结果表明：当造纸白泥添加量为4g／（L·h）时,曝气12h后,pH可达10．19,此时PO4^3-P和NH3-N回收率分别达到64％和45％;而当粉煤灰添加量为4g／（L·h）时,曝气12h后,pH达到9．63,PO4^3-P和NH3-N回收率分别为46％和41％。但仅用曝气方式处理,12h后,pH值仅为8．52,PO4^3-P和NH3-N回收率分别只有20％和18％。实验结果还表明,水力停留时间（HRT）越大,pH上升速度越快,幅度越大,氮磷的回收效果就越好。     

活性污泥超声波预处理的降解特性与减量研究

采用超声波处理序批式间歇反应器(SBR)中的活性污泥,通过改变活性污泥的超声波处理比例,分析SBR系统的污泥降解特性和减量效率。研究结果表明,超声波处理能有效促进系统污泥减量和污泥稳定,30%的处理比例使污泥表观产率和挥发性悬浮固体/悬浮固体(VSS/SS)较对照处理分别减少28%和5.1%,但处理系统出水水质轻微下降,30%和40%的处理比例使系统出水COD去除率较对照处理分别下降了9.5%和12.3%,出水浊度也出现了轻微增加,而污泥的沉降性能并没有产生明显影响。     

Monitoring of natural and synthetic hormones in a polluted river

Natural (estradiol, estrone, testosterone, estriol) and synthetic hormones (ethinylestradiol) are constantly excreted into the environment from human and animal sources but little is known of their transport. The purpose of this study was to determine how far along a 100 km river course that hormones could be detected after contamination with sewage effluent or fishpond effluent. Fourteen sites in the Lower Jordan River drainage were sampled (two sites above the sewage effluent contamination, eight sites below the contamination and four tributaries) before and after the dry season of 2002 (Spring and Fall). Samples were tested for testosterone, estrogen (estrone and estradiol combined), estriol, ethinylestradiol, ammonia and fecal coli. It was found that the fecal coli count dropped exponentially (from 250,000 to 60/100 ml3) and the ammonia dropped from 15 to less than 1mg/l over the initial 25 km stretch. Over the same stretch, the hormone values declined by half from their maximum values for testosterone (3.3 ng/l), estriol (8.8 ng/l), ethinylestradiol (6.1 ng/l), and estrogen (4.9 ng/l). From 67 to 100 km mark, testosterone (4.8 ng/l) and estrogen (2.4 ng/l) were still elevated while ethinylestradiol and estriol were >or=1.5 ng/l. The high level of testosterone and estrogen between 67 and 100 km marks was probably due to major discharge from fishponds between 23 and 27 km marks. Levels of ethinylestradiol above 1 ng/l, a level which can affect fish, was seen in 70% (12/16) of the samples tested. The data suggest that hormones in readily measured quantities can be transported considerable distances from the source of pollution.