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261.
Xian-De Xie Xiao-Bo Min Li-Yuan Chai Chong-Jian Tang Yan-Jie Liang Mi Li Yong Ke Jie Chen Yan Wang 《Environmental science and pollution research international》2013,20(9):6050-6058
Floatation tailings (FT) are the main by-products of the hydrothermal sulfidation–flotation process. FT (FT1 and FT2) were obtained by treating two different neutralization sludges (NS) (NS1 and NS2). This paper quantitatively evaluated the environmental risks of heavy metals (Zn, Cd, Cu, Pb, and As) in FT versus NS. The total concentration and leaching rates (R 2) of heavy metals in FT were much lower than those in NS, demonstrating that the hydrothermal sulfidation–flotation process was able to effectively suppress the mobility and leachability of heavy metals. The BCR-three sequence leaching procedure of FT confirmed that all metals were transformed into more stable forms (residue and oxidizable forms) than were found that in NS. The potential ecological risk index indicated that the overall risks caused by heavy metals decreased significantly from 6627.59 and 7229.67 (very serious risk) in NS1 and NS2, respectively, to 80.26 and 76.27 (low risk) in FT1 and FT2, respectively. According to the risk assessment code, none of the heavy metals in FT posed significant risk to the natural environment except Zn (with low risk). In general, the risk of heavy metals in FT had been well controlled. 相似文献
262.
X. Q. Liang Z. Y. Nie M. M. He R. Guo C. Y. Zhu Y. X. Chen Küppers Stephan 《Environmental science and pollution research international》2013,20(10):6972-6979
One strategy to combat nitrate (NO3-N) contamination in rivers is to understand its sources. NO3-N sources in the East Tiaoxi River of the Yangtze Delta Region were investigated by applying a 15N–18O dual isotope approach. Water samples were collected from the main channel and from the tributaries. Results show that high total N and NO3-N are present in both the main channel and the major tributaries, and NO3-N was one of the most important N forms in water. Analysis of isotopic compositions (δ 18O, δD) of water suggests that the river water mainly originated from three tributaries during the sampling period. There was a wide range of δ 15N-NO3 (?1.4 to 12.4 ‰) and a narrow range of δ 18O-NO3 (3.7 to 9.0 ‰) in the main channel waters. The δ 15N and δ 18O-NO3 values in the upper, middle, and lower channels along the river were shifted as 8.2, 3.5, and 9.5 ‰, and 9.0, 4.2, and 6.0 ‰, respectively. In the tributary South Tiao, the δ 15N and δ 18O-NO3 values were as high as 9.5 and 7.0 ‰, while in the tributaries Mid Tiao and North Tiao, NO3-N in most of the samples had relatively low δ 15N and δ 18O-NO3 values from 2.3 to 7.5 ‰ and 4.7 to 7.0 ‰, separately. Our results also suggest that the dual isotope approach can help us develop the best management practice for relieving NO3-N pollution in the rivers at the tributary scale. 相似文献
263.
H(+)/phenanthrene symporter and aquaglyceroporin are implicated in phenanthrene uptake by wheat (Triticum aestivum L.) roots 总被引:1,自引:0,他引:1
Zhan X Zhang X Yin X Ma H Liang J Zhou L Jiang T Xu G 《Journal of environmental quality》2012,41(1):188-196
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants that are toxic to human and nonhuman organisms. Dietary intake of PAHs is a dominant route of exposure for the general population because food crops are a major source of dietary PAHs. The mechanism for crop root uptake of PAHs remains unclear. Here we reveal that wheat root uptake of PAHs involves active and passive processes. The passive uptake is mercury and glycerol dependent. Mercury and glycerol inhibit uptake, indicating that aquaglyceroporins sensitive to mercury contribute to passive uptake. Active uptake is mediated by a phenanthrene/H symporter. The electrical response of wheat roots triggered by phenanthrene consists of two sequential phases: depolarization followed by repolarization. The depolarization is phenanthrene concentration dependent, with saturation kinetics that have an apparent of K(m) 10.8 μmol L(-1). As uptake proceeds, external solution pH increase is noticed. Lower pH favors the uptake. Vanadate and 2,4-dinitrophenol suppress the electrical response to phenanthrene and phenanthrene uptake, suggesting that plasma membrane H(+)-ATPase is involved in the establishment of an electrochemical proton gradient acting as a driving force for active uptake. Therefore, it is suggested that aquaglyceroporin and phenanthrene/H symporter are implicated in phenanthrene uptake. Our results provide insight into PAH uptake mechanism in wheat roots that is relevant to strategies for reducing PAH accumulation in wheat for food safety, improving phytoremediation of PAH-contaminated soils or water by agronomic practices and genetic modification to target remedial plants for higher PAH uptake capacity. 相似文献
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265.
能源是现代社会发展的重要基础,其在社会经济发展中占有不可替代的地位。以四川省统计年鉴及相关数据资料为基础,参考美国能流图绘制了四川省2010年的能流图,并对四川省2005~2010年间的能源输入、输出、消耗,以及相应的污染物排放进行了分析,分析发现:近年来能源消费总量增长迅速,年均增长率达10.8%,能源对外依存度较高,尤其是石油。能源消耗结构有待进一步优化,传统化石能源所占比重偏高,2010年达77.18%。同时构建了能源-社会经济-环境复合系统能流分析指标,分析了2005~2010年四川省能源、经济、环境两两子系统及三者系统之间的协调度,结果显示:四川省能源-经济-环境系统协调度不断上升,2010年三者综合协调度0.97238。最后根据能流分析、污染物排放水平、协调度分析等结果,提出了四川省能源发展战略、能流的优化管理、节能减排等对策建议。 相似文献
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268.
A rapid spectrophotometric determination of persulfate anion in ISCO 总被引:10,自引:0,他引:10
Due to a gradual increase in the use of persulfate as an in situ chemical oxidation (ISCO) oxidant, a simple measurement of persulfate concentration is desirable to analyze persulfate distribution at designated time intervals on/off a site. Such a distribution helps evaluate efficacy of ISCO treatment at a site. This work proposes a spectrophotometric determination of persulfate based on modification of the iodometric titration method. The analysis of absorption spectra of a yellow color solution resulting from the reaction of persulfate and iodide in the presence of sodium bicarbonate reveals an absorbance at 352 nm, without significant interferences from the reagent matrix. The calibration graph was linear in the range of persulfate solution concentration of 0-70 mM at 352 nm. The proposed method is validated by the iodometric titration method. The solution pH was at near neutral and the presence of iron activator does not interfere with the absorption measurement. Also, analysis of persulfate in a groundwater sample using the proposed method indicates a good agreement with measurements by the titration method. This proposed spectrophotometric quantification of persulfate provides a simple and rapid method for evaluation of ISCO effectiveness at a remediation site. 相似文献
269.
In situ iron activated persulfate oxidative fluid sparging treatment of TCE contamination--a proof of concept study 总被引:1,自引:0,他引:1
In situ chemical oxidation (ISCO) is considered a reliable technology to treat groundwater contaminated with high concentrations of organic contaminants. An ISCO oxidant, persulfate anion (S(2)O(8)(2-)) can be activated by ferrous ion (Fe(2+)) to generate sulfate radicals (E(o)=2.6 V), which are capable of destroying trichloroethylene (TCE). The property of polarity inhibits S(2)O(8)(2-) or sulfate radical (SO(4)(-)) from effectively oxidizing separate phase TCE, a dense non-aqueous phase liquid (DNAPL). Thus the oxidation primarily takes place in the aqueous phase where TCE is dissolved. A bench column study was conducted to demonstrate a conceptual remediation method by flushing either S(2)O(8)(2-) or Fe(2+) through a soil column, where the TCE DNAPL was present, and passing the dissolved mixture through either a Fe(2+) or S(2)O(8)(2-) fluid sparging curtain. Also, the effect of a solubility enhancing chemical, hydroxypropyl-beta-cyclodextrin (HPCD), was tested to evaluate its ability to increase the aqueous TCE concentration. Both flushing arrangements may result in similar TCE degradation efficiencies of 35% to 42% estimated by the ratio of TCE degraded/(TCE degraded+TCE remained in effluent) and degradation byproduct chloride generation rates of 4.9 to 7.6 mg Cl(-) per soil column pore volume. The addition of HPCD did greatly increase the aqueous TCE concentration. However, the TCE degradation efficiency decreased because the TCE degradation was a lower percentage of the relatively greater amount of dissolved TCE by HPCD. This conceptual treatment may serve as a reference for potential on-site application. 相似文献
270.
针对地下储库受限空间的特点和油气爆炸抑制的需要.在前期所完成的系统油气爆炸试验和理论研究的基础上,采用超细冷气溶胶抑爆新技术,建立地下受限空间油气爆炸及其抑爆模拟试验系统,研制出新型超细冷气溶胶粉体抑爆剂,并对其进行可行性与有效性研究.对地下受限空间油气爆炸抑制的影响因素进行研究,分析了抑爆剂作用机理.结果表明:超细冷气溶胶是一种高效的抑制地下储库油气爆炸的抑爆剂;在相同试验条件下,迎着火焰传播方向喷射抑爆剂的抑爆效果优于垂直火焰传播方向喷射抑爆剂;喷射压力存在临界值,较小较大都不利于油气爆炸抑制,在本文试验条件下.最佳抑爆效果的喷射压力临界值约为0.8 Mpa;抑爆剂用量不能低于临界抑爆浓度,实验得到的抑爆刑临界浓度为0.232 ks/m3;布置方式对抑爆效果具有明显的影响.分散布置比集中布置具有更好的抑爆效果.本文的研究对后续抑爆装置的研制提供了重要的理论参考和关键设计参数. 相似文献