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891.
Po Neng Chiang Ming Kuang Wang Pan Ming Huang Jeng Jong Wang 《Journal of environmental radioactivity》2010,101(6):472-481
The dynamics of Cs and Sr sorption by soils, especially in the subtropics and tropics, as influenced by soil components are not fully understood. The rates and capacities of Cs and Sr sorption by selected subtropical and tropical soils in Taiwan were investigated to facilitate our understanding of the transformation and dynamics of Cs and Sr in soils developed under highly weathering intensity. The Langmuir isotherms and kinetic rates of Cs and Sr sorption on the Ap1 and Bt1 horizons of the Long-Tan (Lt) and the A and Bt1 horizons of the Kuan-Shan (Kt), Mao-Lin (Tml) and Chi-Lo (Cl) soils were selected for this study. Air-dried soil (<2 mm) samples were reacted with of 7.5 × 10−5 to 1.88 × 10−3 M of CsCl (pH 4.0) or 1.14 × 10−4 to 2.85 × 10−3 M of SrCl2 (pH 4.0) solutions at 25 °C. The sorption maximum capacity (qm) of Cs by the Ap1 and Bt1 horizons of the Lt soil (62.24 and 70.70 mmol Cs kg−1 soil) were significantly (p < 0.05) higher than those by the A and Bt1 horizons of the Kt and Cl soils (26.46 and 27.49 mmol Cs kg−1 soil in Kt soil and 34.83 and 29.96 mmol Cs kg−1 soil in Cl soil, respectively), however, the sorption maximum capacity values of the Lt and Tml soils did not show significant differences. The amounts of pyrophosphate extractable Fe (Fep) were correlated significantly with the Cs and Sr sorption capacities (for Cs sorption, r2 = 0.97, p < 1.0 × 10−4; for Sr sorption, r2 = 0.82, p < 2.0 × 10−3). The partition coefficient of radiocesium sorbed on soil showed the following order: Cl soil ? Kt soil > Tml soil > Lt soil. It was due to clay minerals. The second-order kinetic model was applied to the Cs and Sr sorption data. The rate constant of Cs or Sr sorption on the four soils was substantiality increased with increasing temperature. This is attributable to the availability of more energy for bond breaking and bond formation brought about by the higher temperatures. The rate constant of Cs sorption at 308 K was 1.39-2.09 times higher than that at 278 K in the four soils. The activation energy of Cs and Sr sorbed by the four soils ranged from 7.2 to 16.7 kJ mol−1 and from 15.2 to 22.4 kJ mol−1, respectively. Therefore, the limiting step of the Cs+ or Sr2+ sorption on the soils was diffusion-controlled processes. The reactive components, which are significantly correlated with the Langmuir sorption maxima of Cs and Sr by these soils, substantially influenced their kinetic rates of Cs and Sr sorption. The data indicate that among components of the subtropical and tropical soils studied, short-range ordered sesquioxides especially Al- and Fe-oxides complexed with organics play important roles in influencing their capacity and dynamics of Cs and Sr sorption. 相似文献
892.
Bioremediation of strontium (Sr) contaminated aquifer quartz sand based on carbonate precipitation induced by Sr resistant Halomonas sp 总被引:3,自引:0,他引:3
Contamination of aquifers or sediments by radioactive strontium (90Sr) is a significant environmental problem. In the present study, microbially induced calcite precipitation (MICP) was evaluated for its potential to remediate strontium from aquifer quartz sand. A Sr resistant urease producing Halomonas sp. was characterized for its potential role in bioremediation. The bacterial strain removed 80% of Sr from soluble-exchangeable fraction of aquifer quartz sand. X-ray diffraction detected calcite, vaterite and aragonite along with calcite-strontianite (SrCO3) solid solution in bioremediated sample with indications that Sr was incorporated into the calcite. Scanning electron micrography coupled with energy-dispersive X-ray further confirmed MICP process in remediation. The study showed that MICP sequesters soluble strontium as biominerals and could play an important role in strontium bioremediation from both ecological and greener point of view. 相似文献
893.
Zhang H Mu W Hou Z Wu X Zhao W Zhang X Pan H Zhang S 《Journal of environmental science and health. Part. B》2012,47(3):153-160
By enrichment culturing of the sludge collected from the industrial wastewater treatment pond, we isolated a highly efficient nicosulfuron degrading bacterium Serratia marcescens N80. In liquid medium, Serratia marcescens N80 grows using nicosulfuron as the sole nitrogen source, and the optimal temperature, pH values, and inoculation for degradation are 30-35°C, 6.0-7.0, and 3.0% (v/v), respectively. With the initial concentration of 10 mg L?1, the degradation rate is 93.6% in 96 hours; as the initial concentrations are higher than 10 mg L?1, the biodegradation rates decrease as the nicosulfuron concentrations increase; when the concentration is 400 mg L?1, the degradation rate is only 53.1%. Degradation follows the pesticide degradation kinetic equation at concentrations between 5 mg L?1 and 50 mg L?1. Identification of the metabolites by the liquid chromatography/mass spectrometry (LC/MS) indicates that the degradation of nicosulfuron is achieved by breaking the sulfonylurea bridge. The strain N80 also degraded some other sulfonylurea herbicides, including ethametsulfuron, tribenuron-methyl, metsulfuron-methyl, chlorimuron-ethyl,and rimsulfuron. 相似文献
894.
Mercury emission and plant uptake of trace elements during early stage of soil amendment using flue gas desulfurization materials 总被引:2,自引:0,他引:2
Cheng CM Chang YN Sistani KR Wang YW Lu WC Lin CW Dong JH Hu CC Pan WP 《Journal of the Air & Waste Management Association (1995)》2012,62(2):139-150
A pilot-scale field study was carried out to investigate the distribution of Hg and other selected elements (i.e., As, B, and Se), i.e., emission to ambient air, uptake by surface vegetation, and/or rainfall infiltration, after flue gas desulfurization (FGD) material is applied to soil. Three FGD materials collected from two power plants were used. Our results show Hg released into the air and uptake in grass from all FGD material-treated soils were all higher (P < 0.1) than the amounts observed from untreated soil. Hg in the soil amended with the FGD material collected from a natural oxidation wet scrubber (i.e., SNO) was more readily released to air compared to the other two FGD materials collected from the synthetic gypsum dewatering vacuum belt (i.e., AFO-gypsum) and the waste water treatment plant (i.e., AFO-CPS) of a forced oxidation FGD system. No Hg was detected in the leachates collected during the only 3-hour, 1-inch rainfall event that occurred throughout the 4-week testing period. For every kilogram of FGD material applied to soil, AFO-CPS released the highest amount of Hg, B, and Se, followed by SNO, and AFO gypsum. Based on the same energy production rate, the land application of SNO FGD material from Plant S released higher amounts of Hg and B into ambient air and/or grass than the amounts released when AFO-gypsum from Plant A was used. Using FGD material with lower concentration levels of Hg and other elements of concern does not necessary post a lower environmental risk. In addition, this study demonstrates that considering only the amounts of trace elements uptake in surface vegetation may under estimate the overall release of the trace elements from FGD material-amended soils. It also shows, under the same soil amendment conditions, the mobility of trace elements varies when FGD materials produced from different processes are used. 相似文献
895.
896.
基于催化剂在线增活工艺,以火电厂运行条件下的典型钒钛类失活催化剂为原料,采用单因素变量法展开了钒基活化液各成分对失活催化剂增活效果的研究,对活化液增活后的催化剂进行活性评价及SEM、BET、FT-IR和XRD等分析,考察增活前后NO转换率、催化剂表面形貌及结构的变化情况。研究结果表明,在实验条件下,随着4种活性成分含量的增加,催化剂增活后NO转换率均呈现先升高后降低的规律,NO转换率最高达99%,且增活后催化剂表面活性成分增加,Brnsted酸性位增多,比表面积增加,对烟气具有较强适应力。 相似文献
897.
实验主张将餐厨固体垃圾和餐厨废水分开处理,并研究微生物燃料电池(MFC)作为餐厨废水和堆肥渗滤液处理工艺的可行性,通过调节不同的有机负荷,分析其生物产电的潜力和处理效率。对于餐厨废水而言,3 000 mg/L是较为理想的处理浓度,输出电压最高,始终维持在0.5 V以上;高于此浓度时电压输出特性与底物浓度呈现反相关,输出电压略低于0.5 V。极化曲线,电化学阻抗分析等也都表明3 000 mg/L是较为理想的处理浓度。而且在各种浓度下经MFC处理后的餐厨废水去除率均在90%左右,出水COD均低于400 mg/L。至于堆肥渗滤液,虽然在产电性能、去除效果上较餐厨废水稍差一些,但整体上与餐厨废水呈现出相似的规律。以上结果表明,餐厨垃圾中的废水可以通过MFC有效的去除和实现能量的回收。 相似文献
898.
Xiao-Song He Bei-Dou Xi Xiang Li Hong-Wei Pan Da An Shuo-Guo Bai Dan Li Dong-Yu Cui 《Chemosphere》2013
The present several humification indexes cannot provide the whole fluorescence information on organic matter composition and the evaluation results from them are inconsistent sometimes. In this study, fluorescence excitation–emission matrix spectra coupled with parallel factor analysis and fluorescence regional integration analysis were utilized to investigate organic matter humification, and the projection pursuit cluster (PPC) model was applied to form a suitable index for overcoming the difficulties in multi-index evaluation. The result showed that the ratio between the volume of humic- and fulvic-like fluorescence region and the volume of protein-like fluorescence region not only revealed the heterogeneity of organic matter, but also provided more accurate information on organic matter humification. In addition, the results showed that the PPC model could be used to characterize integrally the humification, and the projected characteristic value calculated from the PPC model could be used as the integrated humification evaluation index. 相似文献
899.
焦化项目大气污染特征及环境影响评价 总被引:2,自引:0,他引:2
以甘肃省酒泉市阿克塞哈萨克族自治县某焦化项目为案例,在分析其工艺流程和排污环节的基础上,利用AERMOD模型定量预测评价该焦化项目对区域大气环境质量的影响程度。预测结果表明:SO2,NO2,NH3,H2S的区域最大地面小时质量浓度占标率分别为15.8%,29.6%,16.8%,24.8%;SO2、NO2、苯并[a]芘、固体悬浮物(TSP)的区域最大日均质量浓度占标率分别为7.5%,11.4%,7.2%,95.8%;TSP最大日均质量浓度坐标点为(500,0),位于厂界内部,高浓度是由焦化厂低矮面源造成的,且浓度随距离消减得较快。 相似文献
900.
Zhiqiang Zhang Pan Wang Jiao Zhang Siqing Xia 《Environmental science and pollution research international》2014,21(18):10823-10829
The removal and mechanism of Cu2+ and Cd2+ from aqueous single-metal solutions were investigated by using a novel biosorbent from waste-activated sludge. A series of adsorption experiments was designed to disclose the effects of the key factors on the adsorption capacity of the biosorbent for the metal ions. The mass ratio of the biosorbent to metal ion was optimized as 2 to balance the adsorption capacity and the removal efficiency. A right shaking speed (150 r/min) not only ensured enough contact frequency between the sorbent and the adsorbate but also reduced the mass transfer resistance. The natural pH value (about 5.5) of the metal solutions benefited a high adsorption capacity of the biosorbent and avoided the consumption of acid or base for pH adjustment. The adsorption reactions belonged to the endothermic process between 15 and 45 °C. As the scanning electron microscopy (SEM) images showed, the meshy structure with long chains and many branches was ideal for the biosorbent to quickly capture the metal ions. The energy-dispersive X-ray (EDX) spectra confirmed that the adsorbed metal ions lay in the precipitates of the adsorption reactions. According to the FTIR analyses, the functional groups responsible for Cu2+ adsorption majorly consisted of O–H, N–H, COOH, CONH2, and the groups containing sulfur and phosphorus, while those for Cd2+ adsorption contained O–H, N–H, COOH, and CONH2. The differences in the responsible functional groups explained the phenomenon that the adsorption capacity of the biosorbent for Cu2+ was higher than that for Cd2+. 相似文献