In-situ electrochemical measurements of total concentration and speciation of heavy metals in acid mine drainage (AMD): assessment of the use of anodic stripping voltammetry

We assessed the use of anodic stripping voltammetry (ASV) for in-situ determinations of both total concentration and speciation of dissolved heavy metals (Cd, Cu, Pb and Zn) in acid mine drainage (AMD). In the Kwangyang Au–Ag mine area of South Korea, different sites with varying water chemistry within an AMD were studied with a field portable anodic stripping voltammeter. Anodic stripping voltammetry after wet oxidation (acidification) was very sensitive enough to determine total concentration of dissolved Cd because Cd was dominantly present as ‘labile’ species, whilst the technique was not so effective for determining total Cu especially in the downstream sites from the retention pond, due to its complexation with organic matter. For dissolved Pb, the concentrations determined by ASV after wet oxidation generally agreed with those by ICP-AES. In the downstream samples (pH>5), however, ASV data after wet oxidation were lower than ICP-AES data because a significant fraction of dissolved Pb was present in those samples as ‘inert’ species associated with colloidal iron oxide particles. The determination of total dissolved Zn by ASV after wet oxidation appeared to be unsatisfactory for the samples with high Cu content, possibly due to the interference by the formation of Zn–Cu intermetallic compounds on the mercury coated electrode. In AMD samples with high dissolved iron, use of ultraviolet irradiation was not effective for determining total concentrations because humate destruction by UV irradiation possibly resulted in the removal of a part of dissolved heavy metals from waters through the precipitation of iron hydroxides.     

Effect of natural organic matter on arsenic release from soils and sediments into groundwater

Arsenic (As) contamination in groundwater has received significant attention recently. Natural and anthropogenic sources contribute to the worldwide occurrence of As contamination. As speciation is an important factor related to its toxic and mobile behavior. The release of As from soils and sediments into groundwater is governed by several geophysicochemical processes, of which, As sorption behavior is of principle significance. This review paper summarizes existing information regarding the effects of natural organic matter (NOM) on the fate and mobility of As species in the environment. NOM may enhance the release of As from soils and sediments into the soil solution, thereby facilitating As leaching into the groundwater. The main influencing mechanisms include competition for available adsorption sites, formation of aqueous complexes, and/or changes in the redox potential of site surfaces and As redox speciation. NOM may also serve as binding agents, thereby reducing As mobility. However, comparably little research has been performed on this aspect. Since most investigations have been done on purified minerals under laboratory conditions, further research involving various geological materials under natural environmental conditions is required. Development of proper geochemical conceptual models may provide means of predicting the role of NOM in arsenic leaching and/or immobilization.     

Copper complexation by tannic acid in aqueous solution

The speciation of titrated copper in a dissolved tannic acid (TA) solution with an initial concentration of 4 mmol organic carbon (OC)/l was investigated in a nine-step titration experiment (Cu/OC molar ratio = 0.0030–0.0567). We differentiated between soluble and insoluble Cu species by 0.45 μm filtration. Measurements with a copper ion selective electrode (ISE) and diffusive gradients in thin films (DGT) were conducted to quantify unbound Cu(II) cations (‘free’ Cu) and labile soluble Cu complexes. For the DGT measurements, we used an APA hydrogel and a Chelex 100 chelating resin (Na form). Insoluble organic Cu complexes (>0.45 μm) was the dominant Cu species for Cu/OC = 0.0030–0.0567 with a maximum fraction of 0.96 of total Cu. At Cu/OC > 0.0100, Cu-catalysed degradation of aggregate structures resulted in a strong increase of free Cu and (labile) soluble Cu complexes with a maximum fraction of 0.28 and 0.32 of total Cu, respectively. Labile (i.e. DGT-detectable) soluble Cu complexes had a relatively high averaged diffusion coefficient (D) in the APA hydrogel (3.50 × 10⁻⁶– 5.58 × 10⁻⁶ cm² s⁻¹).     

CH_4/N_2/O_2预混气激波火焰结构数值预测

研究激波着火现象，推导激波加热点燃可燃气控制方程组。针对甲烷预混气激波火焰结构进行数值模拟，计算了激波燃烧时的压力、温度、及不同组分随时间的变化历程。其中甲烷燃烧采用美国BERKELEY大学GRI-MECH机理，该反应机理包含177个基元反应，涉及32种组分。程序采用美国SANDIA国家实验室发展的大型化学反应动力学软件包CHEMKIN III中相关的模型、子程序和热力学数据库。计算结果表明激波火焰有其自身的结构特征。     

膜吸收器吸收CO2的影响因素研究

采用聚丙烯中空纤维膜吸收器,用水、NaOH和K2CO3 水溶液作为吸收剂进行高浓度CO2 吸收试验,考察了气体流率、吸收剂流率、质量分数以及流动方式对吸收率、传质系数和传质速率的影响.结果表明,随着气体流率增大,CO2的吸收率递减,总传质系数和总传质速率增加.在一定的气体流率下,吸收液流率增大,CO2的吸收率、总传质系数和总传质速率增大;吸收液浓度提高,吸收率增大,总传质系数和总传质速率提高.在气体流率较低时,质量分数为5%和8%的NaOH水溶液为吸收剂时的吸收率、总传质系数和总传质速率比较接近.随着气体流率增大,NaOH质量分数为8%时的吸收率、总传质系数和总传质速率增加的值大大超过NaOH质量分数为5%时增加的值.以水为吸收剂时,气体与吸收剂的流动方式为逆流时的吸收率、总传质系数和总传质速率高于并流时的值.     

化工园区外围控制距离的确定及环境影响减缓措施

指出制定化工园区周边控制距离过程中需要考虑的重要因素,确定了化工园区外围控制距离中的严禁建设区域和缓冲区域的范围,为城市规划中化工园区外围地域的合理规划提出了依据。同时提出减缓化工园区对园区外影响的措施。     

化工园区定量风险评价中危险源初选方法的研究

在进行化工园区定量风险评价中,危险源的梳理和筛选是首要步骤。分析了欧盟ARAMIS方法、荷兰PURPLE BOOK方法和新西兰的HFSP方法在危险源初选中的适用性,指出对于区域危险源初选用HFSP方法可以全面考虑区域中的各类危险源,快速准确地对危险源进行排序,并提出了HFSP方法用于区域危险源初选的调整方法,给出了危险设施单元的定义和进行QRA的选择判据。     

危险化学品生产企业危险源辨识方法研究

随着经济社会的发展和化工行业投资规模快速增长,社会对危化品的关注日益增长,这就加大了企业安全生产压力。危化品生产企业往往存在着诸多危险源,其中化学性危害因素是在危险源辨识过程中需考虑的重点要素。为了正确辨识危险化学品企业的危险源,保障安全运营,本文梳理了危险源的几种分类,包括物理性危害因素、化学性危害因素、生物性危害因素、心理生理性危害因素、行为性危害因素等,并在此基础上重点研究了工作危害分析、安全检查表、危险与可操作性分析等危险源辨识方法。最后以两个危化公司为样本,介绍了危险源辨识方法的具体内容和操作流程,为企业选用正确方法,科学辨识危险源,顺利排查隐患提供依据。     

一种化学物质的热危险性研究

以某一化学物质(ANPyO)为例,探讨了化学物质热危险性分析方法和步骤:建议首先从化学结构上对物质进行初步分析,然后根据化学结构进行理论计算预测,最后在前面研究的基础上,选择和确定采用合适的,比如:DSC/TG、ARC等小药量实验方法,研究化学物质的热危险性.对于ANPyO,通过分子结构可知其为多硝基多氨基芳烃,是具有潜在的燃烧、爆炸危险的活性化学物质.理论计算预测其属于高危险性物质.对其进行DSC/TG、ARC实验,得到绝热分解反应的热力学和动力学参数,自加速分解温度( TSADT)为199℃,热分解开始温度为310.0℃,最大反应速度出现在系统温度771.5℃时,自热分解开始到最大反应速度的时间为23.5min.文中研究可为该化学物质生产、使用和储运安全提供参考.     

化工园区安全规划方法与应用研究

如何进行科学合理的园区安全规划,整体上提高化工园区的安全水平,是当前化工园区发展过程中的一个关键问题。中国安全生产科学研究院研发的化工园区定量风险评价(QRA)技术及其软件通过化工园区各类事故后果计算、事故概率分析获得园区个人风险、社会风险和安全容量等园区整体性风险评价结果,可用于园区选址规划、园区布局规划、园区企业准入规划和园区安全生产一体化规划等,为化工园区土地使用安全规划提供了实用技术方法,在国内几十个化工园区推广应用,取得了良好实际应用效果。