城市老工业区土壤重金属污染状况与健康风险评价

本文对西部某老工业区土壤中As、Pb、Cr、Cd、Hg、Zn的含量、空间分布状况展开了研究,并依据《污染场地风险评估技术导则》对该老工业区的健康风险进行了评价。研究结果表明,该老工业区土壤重金属污染严重,6种元素与陕西土壤背景值相比超标100%,表明其不适宜作为居住用地开发。健康风险评价结果显示,As、Pb、Cr、Cd元素的非致癌风险值分别为3.83、1.7、1.94、1.09,均超过非致癌风险可接受值1,表明该老工业区对人们存在非致癌健康风险;对于致癌风险,As、Cr、Cd元素的致癌风险值远大于致癌风险边界值,分别超过致癌风险值的2个数量级(2.64×10-4)、4个数量级(1.94×10-2)、1个数量级(6.12×10-5),表示As和Cr已经达到了显著致癌风险的水平。     

河南省武陟县大田土壤重金属形态分布及潜在生态风险评价

为了解河南省武陟县大田土壤重金属Cr、Cd、Pb、As、Cu、Se、Ni和Co的形态分布和生态风险情况,在该区域采集了12个表层土壤(0～20cm)样品,采用修正的BCR连续提取法进行形态分析,探讨其生物有效性,并采用Hakanson指数法评价了重金属的潜在生态风险.结果表明,土壤中不同重金属的形态分布差异很大,其中,Cr、As、Ni和Co均主要以残渣态存在,分别占其总量的66.6％、61.4％、50.7％和41.8％;Cu和Se主要以可氧化态存在,分别占其总量的43.8％和67.8％;Pb主要以可还原态存在,占总量的61.1％;Cd主要以酸提取态存在,占总量的53.3％.生物有效性分析表明,Cd的可利用态K1为0.933,生物有效性是最大的,对土壤生态系统的潜在危害性较大,其次是Pb和Co;Cu和Se在土壤环境发生变化时,很容易再次释放到外界环境中;Cr、As和Ni不易被外界生物利用.潜在生态风险评价结果显示,以国家土壤环境质量标准二级标准为参比值时,Cr、Cd、Pb、As、Cu和Ni的单项潜在生态风险程度均为轻微,综合潜在生态风险处于轻微等级.     

烧结砖中重金属释放特性研究

通过向黏土中添加重金属试剂,模拟煅烧试验制作烧结砖.采用酸消解试验研究烧结砖中重金属的总量,采用欧盟NEN7371方法测试烧结砖中重金属的有效释放量,采用NEN7375方法进行块状烧结砖浸出试验,研究烧结砖样品中Cr、Ni、As、Cd和Pb的释放特性.结果表明:烧结砖中重金属的有效释放量低于总量,释放率从大到小为Cd、As、Pb、Ni、Cr;在块状浸出过程中,Cr、Ni、As累积释放量达到平衡的时间为16 d,Pb为4d,而Cd的累积释放量一直有上升的趋势;Cr、Ni、As的释放机理主要为扩散控制,Cd为溶解作用,Pb为表面冲刷作用;5种重金属释放速率从大到小为Ni、Cr、Pb、As、Cd.     

L型钢管混凝土芯柱耐火极限研究

火灾高温对结构安全有显著影响,为研究等肢L形钢管混凝土芯柱的耐火极限及其影响因素,利用ABAQUS软件建立合理的高温反应分析模型,在验证模型可靠性基础上,分析了荷载比、截面边长、长细比、荷载偏心率、含钢率等对L形钢管混凝土芯柱耐火极限的影响。研究结果表明:在一定参数范围内,荷载比和截面边长是构件耐火极限的主要影响参数,荷载比越小,截面边长越大,构件的耐火极限越高;长细比和荷载偏心率对其影响较大,长细比和荷载偏心率越小,构件的耐火极限越高;含钢率对其影响不显著。结果可为异形钢管混凝土芯柱的抗火安全设计提供参考。     

综放工作面沿空留巷支护阻力研究

为了计算综放工作面沿空留巷支护阻力,以结构力学理论为基础,分析综放工作面沿空留巷支护阻力计算模型,建立沿空留巷围岩和支护体的结构力学模型,应用超静定结构和静定结构分析支护体与沿空留巷围岩相互作用机制,推导出巷旁支护阻力的计算公式.结果表明,进行沿空留巷支护阻力力学分析时,要考虑顶板极限断裂前和断裂后两种状态下的受力情况,支护阻力与岩层厚度、容重、煤体极限平衡区宽度、跨距、支护体宽度和巷道宽度等因素密切相关.工业性试验表明,该技术的应用是成功而有效的.因此,综放巷内沿空留巷围岩结构力学模型和支护阻力计算公式是合理的,可在类似条件的综放工作面中应用.     

兼氧混合菌对亚甲基蓝废水生物降解实验研究

采用厦门某生物科技有限公司提供的兼氧混合菌为研究对象,利用相关设备进行中试实验,验证了该项技术的可行性。同时探究了重金属对该混合菌种生物降解能力的影响,通过中试实验研究后发现5mg/L的重铬酸钾和硫酸铜均对该混合菌种的生物降解能力有一定的影响,并且硫酸铜的影响大于重铬酸钾。此外该技术对甲基橙、刚果红废水也有一定的生物降解能力,这为兼氧混合菌用于印染废水处理提供了实验依据。     

Cu(II), Fe(III) and Mn(II) combinations as environmental stress factors have distinguishing effects on Enterococcus hirae

Pollution by various heavy metals as environmental stress factors might affect bacteria. It was established that iron (Fe(III)), manganese (Mn(II)) and copper (Cu(II)) ion combinations caused effects on Enterococcus hirae that differed from the sum of the effects when the metals were added separately. It was shown that the Cu^2 +–Fe^3 + combination decreased the growth and ATPase activity of membrane vesicles of wild-type E. hirae ATCC9790 and atpD mutant (with defective F_oF₁-ATPase) MS116. Addition of Mn^2 +–Fe^3 + combinations within the same concentration range had no effects on growth compared to control (without heavy metals). ATPase activity was increased in the presence of Mn^2 +–Fe^3 +, while together with 0.2 mmol/L N,N′-dicyclohexylcarbodiimide (DCCD), ATPase activity was decreased compared to control (when only 0.2 mmol/L DCCD was present). These results indicate that heavy metals ion combinations probably affect the F_OF₁-ATPase, leading to conformational changes. Moreover the action may be direct or be mediated by environment redox potential. The effects observed when Fe^3 + was added separately disappeared in both cases, which might be a result of competing processes between Fe^3 + and other heavy metals. These findings are novel and improve the understanding of heavy metals ions effects on bacteria, and could be applied for regulation of stress response patterns in the environment.     

Enhanced catalytic complete oxidation of 1,2-dichloroethane over mesoporous transition metal-doped γ-Al2O3

High-surface-area mesoprous powders of γ-Al₂O₃ doped with Cu^2 +, Cr^3 +, and V^3 + ions were prepared via a modified sol–gel method and were investigated as catalysts for the oxidation of chlorinated organic compounds. The composites retained high surface areas and pore volumes comparable with those of undoped γ-Al₂O₃ and the presence of the transition metal ions enhanced their surface acidic properties. The catalytic activity of the prepared catalysts in the oxidation of 1,2-dichloroethane (DCE) was studied in the temperature range of 250–400°C. The catalytic activity and product selectivity were strongly dependent on the presence and the type of dopant ion. While Cu^2 +- and Cr^3 +-containing catalysts showed 100% conversion at 300°C and 350°C, V^3 +-containing catalyst showed considerably lower conversion. Furthermore, while the major products of the reactions over γ-alumina were vinyl chloride (C₂H₃Cl) and hydrogen chloride (HCl) at all temperatures, Cu- and Cr-doped catalysts showed significantly stronger capability for deep oxidation to CO₂.     

Piriformospora indica confers cadmium tolerance in Nicotiana tabacum

Piriformospora indica, a root-colonizing endophytic fungus of Sebacinales, promotes plant growth and confers resistance against biotic and abiotic stresses. In order to confirm the influence of P. indica on growth, proline, malondialdehyde (MDA), chlorophyll, and cadmium (Cd) amounts in Nicotiana tabacum under Cd stress, hydroponics, pot and field trials were conducted. The results showed that P. indica can store Cd in plant roots and reduce leaf Cd content, reduce the concentration of MDA, and increase the proline and chlorophyll content and the activities of catalase, peroxidase, and superoxide dismutase under hydroponic Cd stress. RT-PCR analysis showed that the relative expression level of genes Gsh2, TaPCS1, oas1, GPX, and Hsp70 in colonized plants was 4.3, 1.4, 2.9, 1.7, and 6.9 fold higher than in un-colonized plants respectively. Cd exposure significantly reduced un-colonized plants'' agronomic traits compared to P. indica-colonized ones. Our results suggested that P. indica can sequester Cd in roots, so that much less cadmium was transported to leaves, and the increased concentrations of antioxidant enzymes, pigments and proline contents, as well as the higher expression of stress-related phytochelatin biosynthesis genes in P. indica-inoculated plants, may also serve to protect N. tabacum plants against oxidative damage, enhancing Cd tolerance.     

Promoting effect of vanadium on catalytic activity of Pt/Ce–Zr–O diesel oxidation catalysts

A series of Pt–V/Ce–Zr–O diesel oxidation catalysts was prepared using the impregnation method. The catalytic activity and sulfur resistance of Pt–V/Ce–Zr–O were investigated in the presence of simulated diesel exhaust. The effect of vanadium on the structure and redox properties of the catalysts was also investigated using the Brunauer–Emmett–Teller method,X-ray diffraction, H2temperature-programmed reduction, CO temperature-programmed desorption, X-ray photoelectron spectroscopy, and Energy Dispersive Spectroscopy. Results showed that the Pt particles were well dispersed on the Ce–Zr–O carrier through the vanadium isolation effect, which significantly improved the oxidation activity toward CO and hydrocarbons. An electron-withdrawing phenomenon occurred from V to Pt, resulting in an increase in the metallic nature of platinum, which was beneficial to hydrocarbon molecular activation.