酸改性对褐煤半焦脱除烟气中元素态汞性能的影响

为减少燃煤烟气中零价汞的排放,利用HCl和HNO3溶液对褐煤半焦改性研制了一种高效、低成本的吸附剂.运用酸碱滴定、Boehm滴定、BET、SEM和FTIR等技术对半焦吸附剂的表面特性进行表征与分析,利用固定床吸附实验装置及烟气测汞仪在线考察了半焦吸附剂对气态Hg0的吸附特性.结果表明,酸改性使半焦灰分含量降低,增加了半焦比表面积和羧基、酚羟基等官能团含量.酸改性处理可提高半焦对元素态单质汞的脱除效率,特别是盐酸溶液改性褐煤半焦可使吸附温度为140℃时的脱汞效率显著提高,这与改性半焦表面羧基、酚羟基和C-Cl官能团的含量及性质有关,半焦表面这些官能团能为Hg0的化学吸附提供活性位.     

臭氧氧化法应用于燃煤烟气同时脱硫脱硝脱汞的实验研究

在固定床反应器上,以模拟烟气为对象研究了O3对NO和Hg0的去除作用。结果表明:温度低于150℃时O3对NO氧化效率几乎不随温度变化,高于150℃时由于O3分解导致NO氧化效率随温度升高而降低;O3对NO氧化效率随n(O3)/n(NO)增大而升高,当n(O3)/n(NO)超过1.0时增加放缓。O3对Hg0氧化效率随温度升高先增后降,在150℃时效率最高,可达近90%;随n(O3)/n(Hg0)增大而升高,当n(O3)/n(Hg0)超过30000后氧化效率几乎不再增加。当三种污染物同时存在时,O3对Hg0的氧化作用受到一定程度的抑制,但对NO氧化效率与单独被O3氧化时无明显差异。     

基于氮掺杂碳量子点的制备及其对Hg2+的响应

以乙二胺和抗坏血酸为原料,通过一步水热法制备了水溶性的氮掺杂碳量子点(N-CQDs).研究了N-CQDs的形貌特征、光学性能和应用分析.表征结果说明,N-CQDs形态为均匀分散的球形,有明显的晶格条纹,抗光漂白性能良好,表面富有含氧官能团,具有良好的水溶性.此外发现N-CQDs还具有优良的荧光性能和荧光稳定性,量子产率可以高达12.29%.分析得出,Hg²⁺对N-CQDs在1.0—120μmol·L^-1范围内有一定的猝灭效应,可作为Hg²⁺的荧光探针,检出限达230 nmol·L^-1.     

万山汞矿区土壤重金属污染特征及来源解析

以万山汞矿区土壤为研究对象,采用电感耦合等离子体质谱仪和原子荧光光谱仪测定土壤中的重金属含量,分别运用内梅罗综合污染指数（NPI）法和潜在生态风险指数（RI）法评价土壤重金属污染和潜在生态风险,并应用相关性分析、主成分分析和聚类分析对土壤重金属来源进行分析。结果表明：土壤Hg、Cd、As、Pb、Cu、Ni和Zn出现不同程度累积,分别达贵州省背景值的263.61、2.31、1.28、2.11、1.70、1.01和3.52倍;土壤重金属平均NPI为188.00,属于严重污染水平,Hg是主要污染因子;土壤重金属平均RI为10 655.70,属于极强潜在生态风险水平,Hg是主要潜在生态风险因子;土壤中Cu、Ni、Cr主要源于自然活动,As、Pb、Zn主要源于燃煤和交通运输污染,Cd主要源于农业污染,Hg主要源于汞冶炼污染。     

CdSe量子点的合成及其在重金属离子检测中的应用

以3-巯基丙酸（3-MPA）为修饰剂合成了水溶性CdSe量子点,优化了合成条件,并以其为荧光探针建立了水样中Pb²⁺和Hg²⁺的检测方法。实验结果表明：在n（Se）∶n（Cd²⁺）为1∶6、n（Se）∶n（NaBH₄）为1∶3、n（Cd²⁺）∶n（3-MPA）为1∶6、反应pH为11、回流温度为100 ℃、回流时间为60 min的优化条件下合成的量子点荧光性能较优;量子点的荧光猝灭强度与Pb²⁺或Hg²⁺的质量浓度呈良好的线性关系,线性范围分别为0.005~10 mg/L和0.001~1 mg/L,检出限分别为0.003 mg/L和0.001 mg/L,相对标准偏差分别为1.23%和1.29%,可应用于实际水样中Pb²⁺和Hg²⁺的检测。     

Hg(Ⅱ)和Pb(Ⅱ)对海洋单细胞藻的急性毒性效应

近年来,海洋重金属污染日益严重,为考察重金属对海洋藻类的生物毒性效应,进而评估其对海洋生态环境的影响,本研究采用一次性培养的实验方法,测定了2种重金属Hg(Ⅱ)和Pb(Ⅱ)对8种海洋单细胞藻的急性毒性效应,包括赤潮异弯藻(Heterosigma akashiwo Hada)、旋链角毛藻(Chaetoceros curv...     

汞矿区大气汞的流通量与汞干湿沉降研究

应用ＦｌｕｘＣｈａｍｂｅｒ技术评价汞矿,矿渣及附近土壤表面汞的流通量,表明,土壤表面汞的流通量平均为１７３．５ｎｇ．ｈ＾－１．ｍ＾－２,矿均为２３６．６ｎｇ．ｈ＾－１．ｍ＾－２,原矿平均为７０ｎｇ．ｈ＾－１．ｍ＾－２。     

Effect of oxidation treatment on the adsorption and the stability of mercury on activated carbon

Oxidation treatment on the adsorption and the stability of Hg on activated carbon （AC） was inrestigated. Both MnO2-AC and FeCl3-AC were produced during oxidation treatment. The measurement of modified AC＇s mercury adsorption capacity was conducted in a simulated coal-fired flue gas by adsorbing test apparatus. TCLP and column leaching methods were used to test the stability of mercury adsorbed on ACs. The results indicate that the oxidation treatment changed the pore structure of the AC and modified the carbon surface by creating chemical components such as MnO4^-, Mn^4＋, O, NO^3-, Fe^3＋, Cl^-, etc. The Hg sorption capacity on MnO2-AC or FeCl3-AC was about three times higher than that of untreated carbon. In addition, the mercury control cost of each of the formers was about the half cost of the untreated carbon. The stability of Hg absorption was studied, it found that mercury adsorbed on the oxidation treated AC was not better than that of untreated carbon. It could concluded that the insoluble form of Hg is very important to the stability of mercury adsorbed on AC. This study suggests that the FeCl3-AC is the best absorbent for Hg with high adsorption capacity, better Hg adsorption stability in leaching environment, and lower cost among the three ACs tested.     

氢化物原子荧光法同时测定海洋沉积物中的痕量 As和Hg

尝试一次消解海洋沉积物样品,用氢化物原子荧光法同时测定As和Hg。试验了KBH4的浓度、共存离子的影响,优化了仪器条件。方法回收率分别为:As为91.9%~105%、Hg为93.0%~109%,As、Hg的线性范围、检出限分别为0~8μg.L-1和0~800 ng.L-1、0.06μg.L-1和2.65 ng.L-1、RSD为4.7%和5.8%。方法具有操作简单、快速、灵敏度高等优点。     

One century sedimentary records of polycyclic aromatic hydrocarbons, mercury and trace elements in the Qinghai Lake, Tibetan Plateau

Sediments from a remote lake of northeastern Tibetan Plateau were analyzed for polycyclic aromatic hydrocarbons (PAHs) and trace metals. USEPA priority PAHs, ranged from 11 in 1860 to 279 ng g⁻¹ in 2002, while, the deposition fluxes were in the range of 0.2-11.4 ng cm⁻² yr⁻¹. Similarly, from 1860 to 2002, an increased trend of Hg flux was observed (0.5-3.2 ng cm⁻² yr⁻¹). Remarkable increase of PAHs and Hg concentration began from 1970, nearly the same period of the “Reform and Open” Policy had been embarked (1978) in China. Good correlations were found between concentrations of Pb, Zn, Cd, As, Hg, and PAHs, which suggested the sources of these chemicals in the sediment is analogous, likely from anthroprogenic sources. Based on isomer ratios, PAHs in core were dominantly from the incomplete combustion of coal. Owing to the proximity to dust source area (Qaidam Basin) and the close association between PAHs, Hg, Pb, and particle matters, atmospheric dust-transport and deposition might be the main pathways that pollutants enter into Qinghai Lake.