固相萃取和高效液相色谱联用测定污水中的五氯苯酚

采用固相萃取和高效液相色谱相结合的方法对污水中五氯苯酚的含量进行定量检测。结果表明,污水的pH值为4,流速控制在4mL/L以内,C18固相萃取柱对五氯苯酚有良好的吸附保留性能,以2mL的甲醇洗脱,洗脱效率在85%~95%之间。与传统的液液萃取相比,固相萃取的优势在于操作时间缩短、有机溶剂的使用量减少。     

烟道气生物脱硫厌氧段影响因素的研究

采用UASB对烟道气生物脱硫厌氧段中的主要影响因素如水力停留时间、进水浓度和温度进行实验研究。分别从亚硫酸根去除效果和硫化物生成情况两方面考查对反应器运行效果的影响。结果表明,水力停留时间为36h时,SRB对SO32-的还原效果良好;进水SO32-浓度范围在500～800mg/L时,SO32-还原率在88%左右;在实验考察的温度范围内,反应温度为33℃时SO32-还原速率和硫化物产生量最大。     

固相萃取-UPLC-MS/MS法测定环境水体中多种抗生素

采用固相萃取-超高效液相色谱串联质谱法测定环境水样中25种磺胺类和喹诺酮类抗生素,通过优化试验条件,使方法在2.00μg/L～200μg/L范围内线性良好,方法检出限为1.01ng/L～2.85ng/L,7次测定结果的RSD为2.3%～8.0%。将该方法用于自来水和地表水测定,结果均为未检出,高、低质量浓度水平的加标回收率为61.2%～102%。     

HPLC-三重四级杆质谱法测定医疗废水中抗生素残留

采用固相萃取/高效液相色谱-三重四级杆质谱法同时测定医疗废水中的20种超痕量抗生素残留,通过优化试验条件,使方法在100μg/L～100μg/L范围内线性良好,方法检出限为024ng/L～122ng/L。空白水样和实际水样3个质量浓度水平的加标回收率分别为80.2%～108%和75.8%～114%,6次测定结果的RSD分别为2.4%～8.4%和1.7%～8.1%。将该方法用于测定重庆市2家三甲医院医疗废水中的超痕量抗生素残留,结果有11种抗生素检出,其余均为未检出。     

聚氨酯泡沫材料阴燃发展过程的特性分析

分析对比了相同加热条件下的聚氨酯泡沫材料在有氧和无氧气氛下的升温过程,并对不同加热条件下的聚氨酯泡沫材料的阴燃传播速度进行研究.结果表明:沿着反应进行的方向,分离点的温度越来越低,不同热流条件下的温度分离曲线斜率在实验稳定发展段的变化规律表现得很相似,并在分离点出现后,有氧气氛中的该位置温度在短时间内急剧上升;在阴燃不稳定传播阶段时,热解前锋的速度小于氧化前锋的速度,在稳定传播阶段时,热解前锋速度与氧化前锋速度近乎相等.     

页岩气开发对生态环境影响评价模型

针对页岩气特殊的开发方式及环评难度比常规气大的特点,运用"压力-状态-响应"框架模型,建立了页岩气开发对生态环境影响的评价指标体系。引入曲线投影的方式,并将投影寻踪方法和动态聚类方法相结合,提出了曲线投影寻踪动态聚类的定量评价方法;基于样本各指标的曲线投影和动态聚类方法寻找最佳投影方向,并建立相应的生态环境影响评价优化模型。结合全局最优经验指导和信息素交流,采用改进的蚁群算法对优化模型进行求解。该算法维持蚁群的多样性,且收敛性较好,同时也避免出现局部最优。对四川省威远页岩气区块进行了实例分析,结果表明:2010年、2011年和2014年的环评属于差类(4级),2012年和2013年的环评属于中类(3级),其中植被覆盖率、空气质量优良率、地表水质达标率、废水排放量、公众对环境的满意度、二氧化硫排放量和废水排放量达标率等指标对生态环境评价的影响较大。在页岩气开发初期,由于开发技术落后,再加上环保投资不高,环保意识不强,造成生态环境问题较为严重。随着学习借鉴美国的经验,及页岩气的开发技术进一步提高,加上国家对生态环境保护的重视,威远页岩气区块生态环境恶化得到有效的遏制。但开发时间越长,开采难度越大,将会产生更多更大的生态环境问题。分析结果与威远页岩气开发区域的实际情况相符,为页岩气气田生态环境影响评价奠定了科学基础。投影寻踪动态聚类方法具有无需设定参数、操作简单、客观等优点,是页岩气开发对生态环境影响评价的一种新方法。     

模拟车用工况下5kW燃料电池尾气净化系统

模拟了车用工况下燃料电池发动机脉冲式排氢的特点,设计开发了一套质子交换膜燃料电池的尾气净化系统,并以5 kW燃料电池的尾气排放为例,研究其净化效果。研究了电池阳极排放氢气缓冲前后尾气中氢气浓度的变化,以及不同空速条件下氢气的去除效果。结果表明：电堆阳极排放氢气经过缓冲处理后,尾气中氢气浓度趋于平稳,大部分工况下处在2%以下,达到了安全处理的要求;尾气中氢气的去除效果与空速密切相关。对自制的整体式催化剂而言,当空速低于20000 h^-1时,氢气的去除率能达到约95%,而当空速达到39270 h^-1时,氢气的去除率仅为10.9%。鉴于这一问题,提出通过采用尾排空气的分流手段调整催化燃烧反应器对空速的要求,以提高尾气中氢气的去除率。     

降低FCC再生烟气NOx排放助剂的实验室评价

通过采用ACE装置与烟气NOx分析仪器联用的实验室评价方法,可在更接近实际催化裂化反应-再生过程的条件下,评价助剂对再生烟气中NOx的催化转化性能,同时还可考察助剂的加入对催化裂化产品分布的影响。采用该方法对几种降NOx助剂的性能进行了评价,结果表明,在催化剂体系中含有Pt基CO助燃剂的情况下,加入4％的RDNO;助剂后,烟气NOx降低幅度约30％～40％,且催化裂化产品分布基本不受影响。     

Influence of temporally variable groundwater flow conditions on point measurements and contaminant mass flux estimations

Monitoring of contaminant concentrations, e.g., for the estimation of mass discharge or contaminant degradation rates, often is based on point measurements at observation wells. In addition to the problem, that point measurements may not be spatially representative, a further complication may arise due to the temporal dynamics of groundwater flow, which may cause a concentration measurement to be not temporally representative. This paper presents results from a numerical modeling study focusing on temporal variations of the groundwater flow direction. “Measurements” are obtained from point information representing observation wells installed along control planes using different well frequencies and configurations. Results of the scenario simulations show that temporally variable flow conditions can lead to significant temporal fluctuations of the concentration and thus are a substantial source of uncertainty for point measurements. Temporal variation of point concentration measurements may be as high as the average concentration determined, especially near the plume fringe, even when assuming a homogeneous distribution of the hydraulic conductivity. If a heterogeneous hydraulic conductivity field is present, the concentration variability due to a fluctuating groundwater flow direction varies significantly within the control plane and between the different realizations. Determination of contaminant mass fluxes is also influenced by the temporal variability of the concentration measurement, especially for large spacings of the observation wells. Passive dosimeter sampling is found to be appropriate for evaluating the stationarity of contaminant plumes as well as for estimating average concentrations over time when the plume has fully developed. Representative sampling has to be performed over several periods of groundwater flow fluctuation. For the determination of mass fluxes at heterogeneous sites, however, local fluxes, which may vary considerably along a control plane, have to be accounted for. Here, dosimeter sampling in combination with time integrated local water flux measurements can improve mass flux estimates under dynamic flow conditions.     

Screening analysis of volatile organic contaminants in commercial inorganic coagulants used for drinking water treatment

A method for quality screening is suggested to detect volatile impurities in inorganic coagulants that are used for drinking water treatment. Static headspace gas chromatography with mass spectrometry detection (HS–GCMS) is sensitive and selective to detect volatiles in low concentrations. This study has discovered that volatile organic impurities are detectable in ferric and aluminium-based coagulants which are used for drinking water treatment. For ferric chloride, 2-propanol was detected at a level of 17–24 μg ml⁻¹, acetone at 0.7–1.7 μg ml⁻¹, 1,1,1-trichloroacetone at 0.02–0.04 μg ml⁻¹, trichloromethane at 0.01–0.02 μg ml⁻¹ and toluene at 0.01–0.12 μg ml⁻¹. For ferric chloride sulfate, acetone was detected at a level of 0.12 μg ml⁻¹, 1,1,1-trichloroacetone at 0.06–0.08 μg ml⁻¹, trichloromethane at 0.13–0.23 μg ml⁻¹, bromodichloromethane at 0.04–0.06 μg ml⁻¹ and dibromochloromethane at 0.04–0.05 μg ml⁻¹. For aluminium hydroxide chloride, only trichloromethane was detectable, but below the method detection limits (MDL). Although the concentrations of these impurities in commercial coagulants are low, this observation is important and should have impact on water industries for them to pay attention to the chemicals they are using for drinking water production.