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981.
西安市大气中多环芳烃的季节变化及健康风险评价 总被引:1,自引:0,他引:1
对西安市2009年6月-2010年5月空气中的总悬浮颗粒(TSP)和气态样品进行了连续采样,利用GC—MS对16种PAHs进行分析。∑PAHs浓度(气相+颗粒相)范围为39.93~1032.46ng/m^3,平均值为197.34ng/m^3;其中,冬季大气中∑PAHs浓度最大,相对浓度的范围为31.21%~72.98%,而夏季的浓度最小;检测出16种2~6环的PAHs,其中以3—4环为主。利用特征分子比值法和因子分析进行源解析,发现研究区PAHs的主要来源为燃煤和机动车尾气排放。通过苯并(a)芘(BaP)等效毒性(BEQ)和苯并(a)芘等效致癌浓度(BaPE)进行健康风险评价,结果显示,西安大气中PAHs的毒性具有明显的季节差异,特别是秋季和冬季大气中PAHs对人类的健康存在较大的潜在威胁。 相似文献
982.
以γ-Al2O3为载体,以MnxCe1-xO2为催化活性组分,采用浸渍法制备了一系列负载型MnxCe1-xO2/γ-Al2O3催化剂(x=0、0.2、0.4、0.6、0.8、0.9、1),在固定床反应器中评价了催化剂对甲苯的催化燃烧性能。结果表明,MnxCe1-xO2/γ-Al2O3催化剂的催化活性与催化剂的焙烧温度、活性组分MnxCe1-xO2的负载量以及Mn、Ce摩尔比有显著关系,其中焙烧温度550℃、负载量为20%、Mn、Ce摩尔比为4:1时,即MnxCe1-xO2/γ-Al2O3催化剂对甲苯的催化性能最佳,反应温度为180℃时,甲苯的转化率达到95%。并在连续100h的稳定性操作后,催化剂的活性基本无变化。采用XRD、BET以及SEM等分析测试手段对催化剂的结构以及表面进行了表征。 相似文献
983.
Li Lu 《Environmental pollution (Barking, Essex : 1987)》2009,157(6):1794-1799
Reducing the transfer of contaminants from soils to plants is a promising approach to produce safe agricultural products grown on contaminated soils. In this study, 0-400 mg/kg cetyltrimethylammonium bromide (CTMAB) and dodecylpyridinium bromide (DDPB) were separately utilized to enhance the sorption of PAHs onto soils, thereby reducing the transfer of PAHs from soil to soil solution and subsequently to plants. Concentrations of phenanthrene and pyrene in vegetables grown in contaminated soils treated with the cationic surfactants were lower than those grown in the surfactant-free control. The maximum reductions of phenanthrene and pyrene were 66% and 51% for chrysanthemum (Chrysanthemum coronarium L.), 62% and 71% for cabbage (Brassica campestris L.), and 34% and 53% for lettuce (Lactuca sativa L.), respectively. Considering the impacts of cationic surfactants on plant growth and soil microbial activity, CTMAB was more appropriate to employ, and the most effective dose was 100-200 mg/kg. 相似文献
984.
985.
Tao Zhang Qiucheng Li Lili Ding Hongqiang Ren Ke Xu Yonggang Wu Dong Sheng 《环境科学学报(英文版)》2011,23(6):881-890
Chemical precipitation to form magnesium ammonium phosphate (MAP) is an effective technology for recovering ammonium
nitrogen (NH4
+-N). In the present research, we investigated the thermodynamic modeling of the PHREEQC program for NH4
+-N
recovery to evaluate the effect of reaction factors on MAP precipitation. The case study of NH4
+-N recovery from coking wastewater
was conducted to provide a comparison. Response surface methodology (RSM) was applied to assist in understanding the relative
significance of reaction factors and the interactive effects of solution conditions. Thermodynamic modeling indicated that the saturation
index (SI) of MAP followed a polynomial function of pH. The SI of MAP increased logarithmically with the Mg2+/NH4
+ molar ratio
(Mg/N) and the initial NH4
+-N concentration (CN), respectively, while it decreased with an increase in Ca2+/NH4
+ and CO3
2??/NH4
+
molar ratios (Ca/N and CO3
2??/N), respectively. The trends for NH4
+-N removal at different pH and Mg/N levels were similar to the
thermodynamic modeling predictions. The RSM analysis indicated that the factors including pH, Mg/N, CN, Ca/N, (Mg/N) (CO3
2??/N),
(pH)2, (Mg/N)2, and (CN)2 were significant. Response surface plots were useful for understanding the interaction effects on NH4
+-N
recovery. 相似文献
986.
随着世界经济一体化的发展和全球环境保护浪潮的兴起,贸易与环境问题日益得到世界各国政府的关注。文章阐述了环境问题与贸易的关系,并讨论了环境问题对我国对外贸易产生的各种影响。 相似文献
987.
三江源区位于青藏高原腹地,是我国长江、黄河、澜沧江三大河流的发源地.为了准确估算该地区草地生态系统的净生态系统生产力,收集整理了2001—2010年青藏高原10个通量观测站点的观测数据,构建了三江源区草地生态系统NEP(net ecosystem production,净生态系统生产力)估算模型,并在站点尺度进行了模型参数化和精度验证;结合区域尺度气象和遥感数据,估算了三江源区草地生态系统NEP.结果表明:① 2001—2010年三江源区草地生态系统多年平均NEP空间分布具有明显的空间异质性,大部分地区表现为碳汇,NEP(以C计)平均值为41.8 g/(m2·a).② 三江源区草地生态系统NEP呈波动增加趋势,从2001年的20.0 g/(m2·a)增至2010年的82.5 g/(m2·a);除2002年表现为弱碳源外,其余年份均表现为碳汇,并以2010年碳汇能力为最强.③ 2001—2010年三江源区草地生态系统NEP平均年增长率为5.4 g/m2;NEP年际变化率空间分布显示,大部分地区NEP呈增加趋势,仅有东南部和中部部分区域NEP呈下降趋势.研究显示,2001—2010年三江源区草地生态系统表现为碳汇,并且由于气候的暖湿化趋势,碳汇强度总体表现为增强. 相似文献
988.
Removal of phosphate by Fe-coordinated amino-functionalized 3D mesoporous
silicates hybrid materials
Phosphate removal from aqueous waste streams is an important approach to control the eutrophication downstream bodies of water.
A Fe(III) coordinated amino-functionalized silicate adsorbent for phosphate adsorption was synthesized by a post-grafting and metal
cation incorporation process. The surface structure of the adsorbent was characterized by X-ray di raction, N2 adsoropion/desoprotion
technique, and Fourier transform infrared spectroscopy. The experimental results showed that the adsorption equilibrium data were well
fitted to the Langmuir equation. The maximum adsorption capacity of the modified silicate material was 51.8 mg/g. The kinetic data
from the adsorption of phosphate were fitted to pseudo second-order model. The phosphate adsorption was highly pH dependent and
the relatively high removal of phosphate fell within the pH range 3.0–6.0. The coexistence of other anions in solutions has an adverse
e ect on phosphate adsorption; a decrease in adsorption capacity followed the order of exogenous anions: F?? > SO2?? 4 > NO??3 > Cl??. In
addition, the adsorbed phosphate could be desorbed by NaOH solutions. This silicate adsorbent with a large adsorption capacity and
relatively high selectivity could be utilized for the removal of phosphate from aqueous waste streams or in aquatic environment. 相似文献
989.
Chih Ming M Ya Wen Lee Gui Bing Hong Te Li Su Je Lueng Shie Chang Tang Chang 《环境科学学报(英文版)》2011,23(4):687-692
TiO2 nanoparticles, doped with di erent Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO2,
H2PtCl6 6H2O and methanol as the solvents. The physicochemical properties of Pt/TiO2 were investigated by the nitrogen adsorption
and desorption isotherm measurement technique, X-ray di raction analysis and photoluminescence spectra, respectively. Reaction rates
from photocatalytic removal of dichloromethane over Degussa P-25 TiO2 and Pt/TiO2 were evaluated. The average diameter and BET
surface area of the TiO2 catalyst particles were 300 nm and 50 m2/g, respectively. The degradation e ciency was 99.0%, 82.7%, 55.2%,
and 57.9% with TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation e ciency was 99.3%,
79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we
found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that
the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO2 process was capable of
e ciently decomposing gaseous DCM in air. 相似文献
990.