流动注射-火焰原子吸收法快速测定水样化学需氧量

采用流动注射-火焰原子吸收法(FI-FAAS)测定水样化学需氧量.以KMnO4作氧化剂、葡萄糖作基准物质,在95 ℃反应,生成的Mn(Ⅱ)在线分离吸附于阳离子交换树脂微型柱上,用3 mol/L HCl洗脱后,送至火焰原子吸收检测器检测.在反应盘管长500 cm、反应时间30 s的条件下,测定化学需氧量的线性范围为8.00～200.00 mg/L,检出限为2.30 mg/L;采样频率为24次/h,Cl-质量浓度至100 mg/L无干扰,Mg2 质量浓度至1 000 mg/L无干扰;对50.00 mg/L的化学需氧量标样重复测定7次,相对标准偏差为3.37%.用该法测定河水、池塘水和轻度污染工业废水的化学需氧量,获得了与重铬酸盐法(标准方法)基本一致的测定结果.     

高氯废水中的化学需氧量测定方法探讨

针对高氯废水化学需氧量的测定方法以及原理作了阐述，最终确定一种最直接、简便、准确的硫酸汞倍数添加法测定CODcr.     

固相萃取与气相色谱-质谱联用测定水中痕量多环芳烃

采用固相萃取与气相色谱-质谱联用测定水中痕量多环芳烃(PAHs)。通过正交试验,得到最佳固相萃取条件为:上样流速为5mL/min、采用二氯甲烷洗脱、洗脱剂用量为3mL、洗脱流速为2mL/min。测定结果显示,固相萃取与气相色谱—质谱联用技术对萘、菲、荧蒽3种PAHs的检出限为0.03～0.07μg/L,加标回收率为70%～100%,相对标准偏差为3.90%～9.58%。该方法精密度高、准确度好,能满足实际水样中痕量PAHs的测定要求。     

Leaching toxicity of the unfired bricks made by dyestuff-making wastewater coagulation aludge

染料废水混凝污泥处理处置及资源化利用对环境保护和染料生产企业的可持续发展有重要意义.依据《固体废物浸出毒性浸出方法水平振荡法》(HJ 557-2009)和《固体废物浸出毒性浸出方法硫酸硝酸法》(HJ/T 299-2007)对污泥和污泥免烧砖制备浸出液,用分光光度法和化学滴定法测定了浸出液中主要有机污染物(对硝基苯胺、苯胺、间苯二胺和丙烯腈)的含量.结果表明:(1)硅酸盐水泥(样品标记为42.5R、水泥1、水泥2)和铝酸盐水泥(样品标记为CA)对苯胺和间苯二胺的固化效果差别不大；水泥2对对硝基苯胺的固化效果最好:42.5R对丙烯腈的固化效果不如其他3种水泥.(2)对硝基苯胺、苯胺、间苯二胺、丙烯腈经水泥固化后,其浸出毒性均降低.     

药物合成废水处理工程

针对氯唑沙宗、枸橼酸莫沙必利化学原料药合成过程中产生的有机废水浓度高、成分复杂及处理难度大等特点(COD高达80000mg/L左右),采用催化氧化-生物化学方法,试验研究了药物合成废水处理。试验结果表明,该技术对合成废水的COD去除率可达98%,SS去除率可达96%,色度降到50倍左右,其去除率约为98%。该系统运行费用为0.4~0·5元/m3废水。经过3个月的工程运行,表明催化氧化-生物化学处理药物合成废水系统是一种高效率、低能耗、运行管理方便、经济可行的处理方法。处理类似制药废水这样的高浓度有机废液,上述废水处理工艺具有广阔的应用前景。     

自配消解液分光光度法测定污水中的COD

以自配消解液代替ThermoFisher公司AQ4001COD测定系统的专用消解液，比较了自配消解液分光光度法与国家标准重铬酸钾法(GB 11914-1989)测定化学需氧量(COD)的差异。对比试验表明，自配消解液分光光度法测定COD的结果精确度和准确度高，与国家标准方法无显著性差异。自配消解液分光光度法测定水样COD值的相对标准偏差;低量程(30～150 mg/L)为1.38%～2.53%，中量程(0～1 500 mg/L)为0.47%～3.63%，高量程（2 000～15 000 mg/L）为0.17%～3.53%，在国家标准方法测试水样COD值的允许误差范围内。除制革废水外，自配消解液可以代替AQ4001COD测定系统的专用消解液，适用不同量程范围内污水COD的测定。自配消解液分光光度法具有试剂使用量少、速度快、经济、二次污染小等优点，值得在环境科学领域及废水水质监测中推广应用。     

药物合成废水处理工程

针对氯唑沙宗、枸橼酸莫沙必利化学原料药合成过程中产生的有机废水浓度高、成分复杂及处理难度大等特点（COD高达80 000 mg/L左右）,采用催化氧化-生物化学方法,试验研究了药物合成废水处理.试验结果表明,该技术对合成废水的COD去除率可达98%,SS去除率可达96%,色度降到50倍左右,其去除率约为98%.该系统运行费用为0.4～0.5元/m^3废水.经过3个月的工程运行,表明催化氧化-生物化学处理药物合成废水系统是一种高效率、低能耗、运行管理方便、经济可行的处理方法.处理类似制药废水这样的高浓度有机废液,上述废水处理工艺具有广阔的应用前景.     

化学需氧量(COD)测定法存在问题探讨

根据《水利废水标准检验法》一书的定义,化学需氧量(COD)是指“测定样品中易受强化学氧化剂氧化的有机物在氧化时所需的氧当量”,普遍使用重铬酸钾为氧化剂。尽管该法使用时间已近百年,且其内容不断得到完善,但至今仍存在许多不尽人意之处。下面仪就共存在的主要问题作一简单讨论。 一、无机还原物的干扰 根据上述定义,化学需氧量是表示废水中有机物含量的。由于废水中有机组分复杂,种类繁多,很难一一定性和定量测定,因此,以化学需氧量作为废水有机污染的综合指标是很有实际意义的。但是,废水中的某些无机还原性物质如亚铁盐、硫化物、亚硝酸盐、亚硫酸盐、硫代硫酸盐、氯离子等均能被重铬酸钾氧     

黄磷诱发的臭氧与紫外光联合处理有机废水研究

主要通过对制药废水、毛纺厂废水和模拟邻氯苯酚废水进行POZONE和POZONE／UV法处理的研究，详细地考察了POZONE与POZONE／UV法处理废水的效果，特别是废水生化需氧量／化学需氧量(B／C)的变化。结果表明，POZONE法能在10min内将制药废水的CODCr去除35.6％，POZONE／UV法可以提高邻氯苯酚废水的B／C近3倍，POZONE／UV法处理毛纺废水的效果要优于POZONE法。     

基于响应面分析法的水质中邻苯二甲酸酯检测方法优化

建立了水质中邻苯二甲酸二甲酯(DMP)、邻苯二甲酸二丁酯(DBP)、邻苯二甲酸二辛酯(DOP)的前处理及反相超高效液相色谱检测方法，通过单因素试验考察了色谱柱类型、流动相类型、流动相体积分数、流速及柱温对主峰信噪比的影响，并采用响应面分析法进行了方案优化。结果表明：氰基色谱柱优于C₁₈色谱柱；在最优色谱条件(流动相乙腈水溶液(体积分数64%)、流速0.22 mL/min、柱温28℃)下，DMP、DBP、DOP的主峰信噪比平均值分别为8 890、6 637、2 991,对应的检出限分别为0.05、0.03、0.08μg/L,均低于《水质邻苯二甲酸二甲(二丁、二辛)酯的测定液相色谱法》(HJ/T 72—2001)规定的检出限，加标回收率分别为98.4%、99.8%和98.0%,相对标准偏差为0.98%、0.52%和0.83%,具有良好的灵敏度、回收率和重复性，能更好满足地下水等水体的痕量检测要求。     

染料废水混凝污泥免烧砖浸出毒性的研究

染料废水混凝污泥处理处置及资源化利用对环境保护和染料生产企业的可持续发展有重要意义。依据《固体废物浸出毒性浸出方法水平振荡法》(HJ 557—2009)和《固体废物浸出毒性浸出方法硫酸硝酸法》(HJ/T 299—2007)对污泥和污泥免烧砖制备浸出液,用分光光度法和化学滴定法测定了浸出液中主要有机污染物(对硝基苯胺、苯胺、间苯二胺和丙烯腈)的含量。结果表明:(1)硅酸盐水泥(样品标记为42.5R、水泥1、水泥2)和铝酸盐水泥(样品标记为CA)对苯胺和间苯二胺的固化效果差别不大;水泥2对对硝基苯胺的固化效果最好;42.5R对丙烯腈的固化效果不如其他3种水泥。(2)对硝基苯胺、苯胺、间苯二胺、丙烯腈经水泥固化后,其浸出毒性均降低。     

Ti/BDD/PbO2复合电极在化学需氧量测定中的应用

以钛基掺硼金刚石为基体,采用电沉积的方法制备了Ti/BDD/PbO2复合电极,并将其用于化学需氧量(COD)的测定。采用扫描电子显微镜(SEM)和X射线衍射谱图(XRD)表征了电极的微观形貌及结构,采用电化学工作站考察了电极对有机物响应特性。实验结果表明,在1.45 V的低电位条件下,线性范围为0.5～175 mg/L,检测限为0.3 mg/L(S/N=3)。采用Ti/BDD/PbO2复合电极测定法和重铬酸钾标准方法对市政污水、食品废水及印染废水的对比结果表明,2种方法的相对误差小于10%,具有良好的一致性。     

Ti/BDD/PbO_2复合电极在化学需氧量测定中的应用

以钛基掺硼金刚石为基体,采用电沉积的方法制备了Ti/BDD/PbO2复合电极,并将其用于化学需氧量（COD）的测定。采用扫描电子显微镜（SEM）和X射线衍射谱图（XRD）表征了电极的微观形貌及结构,采用电化学工作站考察了电极对有机物响应特性。实验结果表明,在1.45 V的低电位条件下,线性范围为0.5～175 mg/L,检测限为0.3 mg/L（S/N=3）。采用Ti/BDD/PbO2复合电极测定法和重铬酸钾标准方法对市政污水、食品废水及印染废水的对比结果表明,2种方法的相对误差小于10%,具有良好的一致性。     

Analysis of volatile and semivolatile organic compounds in municipal wastewater using headspace solid-phase microextraction and gas chromatography.

The aim of this work was to develop a simple and fast analytical method for the determination of a wide range of organic compounds (volatile and semivolatile compounds) in municipal wastewater. The headspace-solid-phase microextraction (HS-SPME) and gas chromatography (with mass spectroscopy) was used for determination of the organic compounds. In this study, 39 organic compounds were determined, including 3 sulfur compounds, 28 substituted benzenes, and 8 substituted phenols. The extraction parameters, such as types of SPME fiber, extraction temperature, extraction time, desorption time, salt effect, and magnetic stirring, were investigated. The method had very good repeatability, because the relative standard deviations ranged from 0.5 to 12%. The detection limit of each compound was at or below the microgram-per-liter level. This method was applied for determination of the organic compounds in raw wastewater, primary effluent, secondary effluent, and chlorinated secondary effluent samples from the Chania Municipal Wastewater Treatment Plant (Crete, Greece).     

A new reliable method for dimethyl sulfoxide analysis in wastewater: dimethyl sulfoxide in Philadelphia's three water pollution control plants.

A simple but reliable procedure was developed to analyze dimethyl sulfoxide (DMSO) in wastewater. The isotope DMSO_d6 was used as the internal standard to ensure accuracy. The DMSO was reduced with stannous chloride and measured as dimethyl sulfide (DMS) with purge-and-trap gas chromatography/mass spectrometry. The method detection limit was at the sub-microgram-per-milliliter level; precision, as measured by standard deviation, was better than +/- 0.5%; and the recoveries were between 95 and 105% at the level of 2 microg/mL. The procedure could use standard analytical instrumentation used for volatile organic compound analysis. A field study was conducted to validate the method and quantify DMSO concentration range in the three water pollution control plants (WPCPs) in the city of Philadelphia, Pennsylvania. Results showed that, when a local chemical facility discharged, DMSO concentration could be as high as 12 mg/L in the influent to a WPCP. This would lead to the formation of a toxic "canned corn" DMS odor during the treatment processes.     

The application of electrochemical technology to the remediation of oily wastewater

The successful application of electrochemical technology, employing a dimensionally stable anode (DSA((R))), for the remediation of wastewater from the oil extraction industry has been demonstrated. Samples from the oil-water separation box of an effluent treatment plant were submitted to voltammetry, chronoamperometry and electrolysis studies using a DSA anode of nominal composition Ti/Ru(0.34)Ti(0.66)O(2). Electrolysis of the oily wastewater lead to a time-dependent reduction in chemical oxygen demand (COD) in the sample that could be attributed to: (i) the direct oxidation of oil components at the electrode, by the metal oxide itself or by OH() radicals available at the electrode surface, (ii) the indirect oxidation of oil components by intermediate oxidising agents formed in parallel reactions (ex. ClO(-)), and (iii) the aggregation of suspended oil droplets by electroflotation. The largest reduction (57%) in COD was obtained following electrolysis of an oily sample for 70 h at 50 degrees C with a current density of 100 mA cm(-2). The stability of DSA electrodes for use in oily wastewater remediation has been assessed.     

微生物膜法快速测定水中的BOD

利用微生物膜法快速测定水中的BOD,用质控样和标液进行方法准确度和精密度的考察,标准偏差在0.9%～5.2%之间,相对误差≤4.0%,加标回收率为95.5%～103%.与接种稀释法进行对比实验,相对误差在1.5%～10.3%范围内,两种方法测定结果基本一致.     

Multivariate optimization of solid-phase extraction applied to iron determination in finished waters

In this work, Amberlite XAD-4 resin functionalized with salicylic acid was synthetized, characterized and applied as a new packing material for an on-line system to iron determination in aqueous samples. The detection method is based on the sorption of Fe(III) ions in a minicolumn containing the synthesized resin, followed by a desorption step using an acid solution and measurement of iron by vis-spectrophotometry (CAS method). The optimization of the solid-phase extraction system was performed using factorial design and Doehlert matrix considering six variables: sample percolation rate (0.5-9 ml min(-1)), sample metal concentration (20-200 microg l(-1)), flow-through sample volume (0-5 ml) (all three directly linked to the extraction step), elution flow-rate (0.5-9 ml min(-1)), concentration and volume of eluent (HCl 0.1-0.5M) (all three directly linked to the elution step). The aim of this study was to obtain a set of operating ranges for the six variables tested in order to obtain--by means of a mathematical function allowing maximisation of each response (desirability function)--at least 90% of iron recovery rates. Using the experimental conditions defined in the optimization, the method allowed iron determination with achieved detection limit of 2.3 microgl(-1) and precision (assessed as the relative standard deviation) of 9.3-2.8% for iron solutions of 10.0-150 microgl(-1). Real samples (coming from a water treatment unit) were used successfully when evaluating potentialities of the developed SPE procedure coupled to a spectrophotometric determination.     

Production of electricity from proteins using a microbial fuel cell.

Electricity generation was examined from proteins and a protein-rich wastewater using a single chamber microbial fuel cell (MFC). The maximum power densities achieved were 354 +/- 10 mW/m2 using bovine serum albumin (BSA) and 269 +/- 14 mW/m2 using peptone (1100 mg/L BSA and 300 mg/L peptone). The recovery of organic matter as electricity, defined as the Coulombic efficiency (CE), was comparable to that obtained with other substrates with CE = 20.6% for BSA and CE = 6.0% for peptone. A meat packing wastewater (MPW), diluted to 1420 mg/L chemical oxygen demand, produced 80 +/- 1 mW/m2, and power was increased by 33% by adding salt (300 mg/L sodium chloride) to increase solution conductivity. A wastewater inoculum generated 33% less power than the MPW inoculum. The MFC was an effective method of wastewater treatment, demonstrated by >86% of biochemical oxygen demand and total organic carbon removal from wastewater.     

A potential new commercial method for processing leather to reduce environmental impact

INTRODUCTION: Current leather processing method involves dehairing and fibre opening employing lime and sulphide, which results in higher negative impact on the environment due to its uncleanness. This method of dehairing and fibre-opening process accounts for nearly 70-80% biochemical oxygen demand and chemical oxygen demand (COD) in tannery wastewater and also the generation of H(2)S gas. MATERIALS AND METHODS: Hence, an attempt has been made to reduce the environmental impact of the leather processing through a biochemical approach, employing proteolytic enzyme and sodium metasilicate for performing the above process more cleanly. RESULTS AND DISCUSSION: The developed process exhibits significant reduction in environmental parametres such as COD and total solid loads by 55% and 25%, respectively. This method completely avoids the formation of lime sludge. CONCLUSION: The functional properties of the leathers are also on par with conventionally processed leathers. Further, the process seems to be commercially viable.