长江口滨岸潮滩无齿相手蟹体内重金属元素的时空分布及其在环境监测中的指示作用

对长江口滨岸带无齿相手蟹体内的重金属元素分析表明:无齿相手蟹体内的Zn、Cr、Ni三种元素季节分布的总体趋势是夏季>春季>秋季。无齿相手蟹对重金属元素的累积也存在着地点间的差异。青龙港、浒浦两地的无齿相手蟹对Cu、Pb、Cr、Ni的累积量都很高,东海农场和崇明东滩的无齿相手蟹对Zn的累积量较高。对无齿相手蟹、沉积物、悬浮颗粒物中的重金属含量分析表明,无齿相手蟹对重金属Cu有一定的富集能力,适于做长江口滨岸带Cu的指示生物。     

贝类帕金虫间接酶联免疫吸附测定法的建立

采用液体巯基醋酸盐培养基(FTM)培养贝类帕金虫,以其制备抗帕金虫的免疫血清,建立一种快速检测贝类帕金虫的间接酶联免疫吸附测定法(iELISA)。方法中理想的包被抗原数量为104/mL;帕金虫抗血清最佳工作浓度1:10 000;酶标二抗工作浓度为1:1 000;进行血清敏感性测定,其最低检出限为102/mL;阻断试验中的阻断率达86.77%;板内和板间变异系数分别为2.9%和3.21%。将该方法标准化后,对30份菲律宾蛤仔体内帕金虫进行检测,所得结果与用FTM方法得到的结果进行比较,后者灵敏度要高于前者,但是在检测时间上,前者在24 h内能够完成,而后者需要7 d。     

Removal of heavy metals from a contaminated soil using tartaric acid

This study reports the feasibility of remediation of a heavy metal （HM） contaminated soil using tartaric acid, an environmentally-friendly extractant. Batch experiments were performed to test the factors influencing remediation of the HM contaminated soil. An empirical model was employed to describe the kinetics of riM dissolution/desorption and to predict equilibrium concentrations of HMs in soil leachate. The changes of HMs in different fractions before and after tartaric acid treatment were also investigated. Tartaric acid solution containing HMs was regenerated by chestnut shells. Results show that utilization of tartaric acid was effective for removal of riMs from the contaminated soil, attaining 50%-60% of Cd, 40%-50% of Pb, 40%-50% of Cu and 20%-30% of Zn in the pH range of 3.5-4.0 within 24 h. Mass transfer coefficients for cadmium （Cd） and lead （Pb） were much higher than those for copper （Cu） and zinc （Zn）. Sequential fractionations of treated and untreated soil samples showed that tartaric acid was effective in removing the exchangeable, carbonate fractions of Cd, Zn and Cu from the contaminated soil. The contents of Pb and Cu in Fe-Mn oxide fraciton were also significantly decreased by tartaric acid treatment. One hundred milliliters of tartaric acid solution containing HMs could be regenerated by 10 g chestnut shells in a batch reactor. Such a remediation procedure indicated that tartaric acid is a promising agent for remediation of HM contaminated soils. However, further research is needed before the method can be practically used for in situ remediation of contaminated sites.     

Selection of appropriate organic additives for enhancing Zn and Cd phytoextraction by hyperaccumulators

Chelant-enhanced phytoextraction is one of the most promising technologies to remove heavy metals from soil. The key of the technology is to choose suitable additives in combination with a suitable plant. In the present study, laboratory batch experiment of metal solubilization, cress seeds germination were undertaken to investigate the metal-mobilizing capability and the phytotoxicity of organic additives, including ethylene diamine triacetic acid （EDTA）, citric acid, acetic acid, oxalic acid, glutamine and monosodium glutamate waste liquid （MGWL） from food industry. Experiments in pots were carried out to study the effects of the additives on Zn and Cd phytoextraction. Furthermore, a leaching experiment with lysimeter was performed to evaluate the environmental risks of additive-induced leaching to underground water. The results showed that EDTA had a strong mobilizing ability for Zn and Cd, followed by mixed reagent （MR） and MGWL. MGWL and acetic acid at 5 mmol equivalent per liter resulted in seed germination index less than 2%. Experiments in pots verified the phytotoxicity of acetic acid and MGWL. Addition of the mixed reagent at 6--10 mmol/kg significantly increased Zn phytoextraction by Thlaspi caerulescens. The same for EDTA and the mixed reagent at 10 mmol/kg by Sedum dfredii. But only mixed reagents could significantly increase Cd phytoextraction by the studied hyperaccumulators. This suggested that the strong chelant was not always the good agent to enhance phytoextraction. S. alfredii combined with 2--10 mmol/kg soil MR was preferred for phytoremediation of Cd/Zn contaminated soils in southern China, this could result in high phytoextraction of Cd/Zn and reduce the leaching risk to underground water than EDTA assisted phytoextration.     

Behavior and control of chlorine in dyestuff residue incineration

Dyestuffresidue, a type of hazardous waste, is incinerated in the tubular furnace, and thermodynamic equilibrium model is used to calculate and analyze the chlorine behavior. The HCI emission and its effects on the behaviors of heavy metals are studied. Meanwhile, the effects of three dechlorine reagents are predicted at a high temperature. Results show that HCI emission is dependent on incineration temperature. The HCl evaporated mainly derives from the organic chlorine. Under the working condition of 500-- 900℃, the main products of rig, Pb, Cu, Ni, Zn, and Mn in reaction with HCl are HgCl2 （g）, PbCl4（g）, PbCI2 （g）, （CuCl）3 （g）, NiCl2 （s）, NiCl2 （g）, ZnCl2 （s）, ZnCl2 （g）, Zn （g）, MnCl2 （s）, and MnCl2 （g）, respectively. Among the three dechlorine reagents, CaCO3 is optimal to remove chlorine at high temperature, little of HCl is released below 800℃, whereas Fe3O4 is unstable at high temperature.     

隧道与横通道交叉角对火灾烟气蔓延影响机制研究

为探索隧道与横通道交叉角对火灾烟气蔓延的影响机制,采用FDS数值模拟,研究横通道与隧道不同交叉角情况下火灾烟气温度、浓度、烟气层高度等的变化规律,建立开启火源下风向横通道时隧道内烟气最高温度修正公式,提出烟气纵向蔓延恢复长度的概念,并探讨其影响规律。 结果表明:隧道和横通道交叉角越小,隧道内同一位置烟气层高度越高,当交叉角由90°降低到30°时,烟气层高度最大增加32%;烟气纵向蔓延恢复长度与交叉角及通风速率呈正相关,而与火源功率几乎无关。研究结果对隧道通风排烟系统设计及相关标准的制定具有参考意义。     

汽车道路试验安全管理体系建设研究

为了保障汽车道路试验安全、提高安全管理水平,设计提出汽车道路试验安全管理体系(SMS)总方案。根据OHSAS 18001和安全标准化规范的特点分析,论证了融合两种体系建立道路试验SMS的适用性。并从政策与目标、风险管理、安全保证和安全促进四个模块阐述了该体系的搭建思路、框架内容和搭建步骤。最后,以某自主品牌车企研发中心道路试验的应用情况为例进行效果评估,结果表明:汽车道路试验SMS能有效防控风险、提升试验安全管理水平。     

Investigating the quantitative and qualitative status of effluent in the wastewater treatment plant in Iran Central Iron Ore

The aim of present study was to investigate the quality of the produced effluent from different units of the Iran Central Iron Ore in Bafq city and comparison of effluent with the standards. This study presents the physicochemical and biological parameters data of effluent of three Sequencing batch reactors (SBR) with a capacity of 160 m³?d^?1. Most common parameters include pH, total suspended solids (TSS), total nitrogen (TN), total phosphorus (TP), biochemical oxygen demand (BOD₅), chemical oxygen demand (COD), heavy metals, and total coliforms and fecal coliforms as biological indicators. Then, for each SBR system, the average of each parameter was determined, and results were compared with the standard recommended by the Iranian Environmental Protection Agency. Based on the results, some of the parameters, including BOD₅, COD, and TSS in the wastewater treatment plant (WWTP) effluent, are higher than the permitted amount for discharge to the surface water. Considering the BOD₅, COD, and TSS concentration in WWTPs, the treated wastewater is only suitable for agricultural and irrigation use. Therefore, wastewater produced by Iran Central Iron Ore Co. will need additional treatment to achieve standard quality of water before discharge in surface water and adsorbent well.     

不同类型活性炭处理废水中重金属离子的研究进展

重金属对人体的显著毒性和难降解的特性,使重金属水体污染成为全球性关注的环境问题。本文综述了重金属废水的危害、来源及常用处理方法,比较了不同类型活性炭处理废水中重金属离子的差异,阐述了不同类型活性炭处理技术的优势和特点,并对今后的重金属废水处理技术研究方向进行了展望。     

Catalytic oxidation of CO over Pt/Fe3O4 catalysts: Tuning O2 activation and CO adsorption

• Strong metal-support interaction exists on Pt/Fe₃O₄ catalysts. • Pt metal particles facilitate the formation of oxygen vacancies on Fe₃O₄. • Fe₃O₄ supports enhance the strength of CO adsorption on Pt metal particles. The self-inhibition behavior due to CO poisoning on Pt metal particles strongly impairs the performance of CO oxidation. It is an effective method to use reducible metal oxides for supporting Pt metal particles to avoid self-inhibition and to improve catalytic performance. In this work, we used in situ reductions of chloroplatinic acid on commercial Fe₃O₄ powder to prepare heterogeneous-structured Pt/Fe₃O₄ catalysts in the solution of ethylene glycol. The heterogeneous Pt/Fe₃O₄ catalysts achieved a better catalytic performance of CO oxidation compared with the Fe₃O₄ powder. The temperatures of 50% and 90% CO conversion were achieved above 260°C and 290°C at Pt/Fe₃O₄, respectively. However, they are accomplished on Fe₃O₄ at temperatures higher than 310°C. XRD, XPS, and H₂-TPR results confirmed that the metallic Pt atoms have a strong synergistic interaction with the Fe₃O₄ supports. TGA results and transient DRIFTS results proved that the Pt metal particles facilitate the release of lattice oxygen and the formation of oxygen vacancies on Fe₃O₄. The combined results of O₂-TPD and DRIFTS indicated that the activation step of oxygen molecules at surface oxygen vacancies could potentially be the rate-determining step of the catalytic CO oxidation at Pt/Fe₃O₄ catalysts. The reaction pathway involves a Pt-assisted Mars-van Krevelen (MvK) mechanism.