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在实验室条件下(27±2℃,REH65±3%),受0.15μg/l和0.50μg/lS-O_2作用的蚜虫死亡率在32小时内与对照组无差异。用0.15,0.50μg/lSO_2薰7天后的莴苣苗饲喂,在为期15天的实验中,0.50μg/1组产仔总数(88.5±5.562)大于对照组(73.3±6.019)和0.15μg/l组(71.5±6.650)。内禀增长率率(?)m0.50>(?)m0.15>(?)m对照。体长在各浓度间无明显差异。实验表明:SO_2对蚜虫种群变动的影响主要是通过寄主植株的生理变化而生产的。 相似文献
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大气中挥发性卤代烃类(VHH)的浓度与工业或商业活动的规模以及人口密度有关。在意大利杜林市测定了VHH_s,算出了一年内它的室内室外含量比和测定了一年中血液内VHH的浓度。结果显示出主要污染物趋势:在冬季为18.1μg/m~3,而夏季为12.02μg/m~3。冬季VHH室内室外含量比显示室内较高(P=0.0006)且VHH在血液中的浓度较高(0.71±0.22μg/L)。在冬季,室内外大气中VHH浓度高是人体摄入VHH的主要来源。 相似文献
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《中国环保产业》2021,(10)
采用安大略法(OHM法)和Method 29法(M29法)测试武汉市4家企业燃煤工业锅炉烟气重金属排放浓度,分析烟气中汞(Hg)、镉(Cd)、铬(Cr)、铅(Pb)、砷(As)的排放特征以及整个过程中重金属的物质流向。结果表明:烟气中重金属Hg、Cd、Pb、As主要以气态形式存在,平均浓度分别为0.35μg/m~3、0.15μg/m~3、3.89μg/m~3和6.07μg/m~3,气态占比分别为100%、96.4%、66.2%和75.7%;烟气中Cr主要以颗粒态形式存在,平均浓度为30.05μg/m~3,颗粒态Cr平均占比为97.2%。飞灰富集Hg、Cr、Pb、As的能力大于炉渣。不同重金属在燃烧过程中的流向存在差异,Hg主要流向飞灰和脱硫副产物,Cr、Pb、As主要流向飞灰和炉渣。 相似文献
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厌氧氨氧化反应器的启动及运行 总被引:11,自引:0,他引:11
采用污泥混合接种的方法 ,成功地启动了实验室规模的厌氧氨氧化反应器 ,启动后含氨模拟废水运行的进水氨浓度和进水亚硝基氮浓度均为 2 0mmol/L ,氨氮、亚硝基氮和总氮的容积负荷率为 10 6 9mmol/L .d、12 2 6mmol/L .d和 394 5 5mg/L .d ,氨氮、亚硝基氮和总氮的去除率保持在 90 %、99%和 95 %以上。对运行条件研究表明 ,厌氧氨氧化反应的最适pH为 7~ 7 5 ,最适温度约在30± 1℃。厌氧氨氧化随亚硝酸盐浓度的升高而下降 ,氨的厌氧转化随COD浓度的增加也呈抑制型曲线 ,当COD浓度为 80 0±5 0mg/L时 ,厌氧氨氧化速率达到最大。 相似文献
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《四川环境》2018,(6)
在川南地区的宜宾市开展了大气细颗粒物(PM_(2.5))浓度及组分的季节观测分析,结果表明,采样点的PM_(2.5)年均浓度(51. 7μg/m~3)超过二级浓度限值47. 71%,同时全年有20. 94%的天数PM_(2.5)日均浓度超过二级浓度限值;冬季浓度最高、达81. 1μg/m~3,明显高于其他季节,夏季浓度最低。PM_(2.5)中水溶性无机离子浓度总和冬(42. 42μg/m~3)秋(32. 73μg/m~3)春(24. 57μg/m~3)夏(17. 0μg/m~3),但占PM_(2.5)浓度的百分比的季节规律则刚好与之相反,为夏(54. 19%)春(48. 1%)秋(46. 91%)冬(45. 45%);其中,SO_4~(2-)、NO_3~-和NH_4~+是PM_(2.5)中最主要的3种二次无机离子组分,三者浓度之和占PM_(2.5)的37. 47%。PM_(2.5)中SO_4~(2-)、NO_3~-和NH_4~+的浓度均为冬季高于其他季节,但NO_3~-/PM_(2.5)冬(12. 22%)秋(11. 53%)春(8. 14%)夏(5. 43%)、NH_4~+/PM_(2.5)秋(9. 85%)夏(9. 15%)春(8. 52%)冬(7. 61%)、SO_4~(2-)/PM_(2.5)夏(26. 3%)春(20. 75%)秋(15. 82%)冬(14. 61%)。四个季节SOR值均大于NOR值,SOR值季节变化差异不大,但NOR值冬季明显高于其他季节。PM_(2.5)中的SO_4~(2-)、NO_3~-和NH_4~+冬季以(NH_4)_2SO_4、NH_4NO_3的形式共存于气溶胶体系中,而夏季则主要以(NH_4)_2SO_4和NH_4HSO_4存在。 相似文献
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《资源开发与市场》2019,(4)
建立超高效液相色谱法(UPLC),测定桦褐孔菌中三种主要化合物原儿茶醛、丁香酸和(E)-4-(3,4-二羟基苯基)丁-3-烯-2-酮含量。采用UPLC法,色谱柱为CORTECS UPLC T3(2. 1mm×100mm,1. 6μm),流动相为乙腈—水(含0. 1%甲酸),柱温为40℃,流速为0. 4mL/min,进样量为1μL,检测波长为280nm。结果表明:原儿茶醛、丁香酸和(E)-4-(3,4-二羟基苯基)丁-3-烯-2-酮分别在0. 1953125—6. 25μg/m L(R2=1. 0000)、0. 1953125—6. 25μg/m L (R2=0.9998)、0. 1953125—6. 25μg/m L(R2=1. 0000)范围内线性关系良好,平均回收率(n=9)分别为98. 150%(RSD=1. 924%)、95. 787%(RSD=2. 487%)、100. 324%(RSD=1. 541%)。不同产地间的桦褐孔菌含量测定结果表明,三种化合物含量的差异较大,吉林长白山最高,俄罗斯西伯利亚次之,黑龙江大兴安岭最低。该方法操作简便、结果准确可靠、重现性好,可为桦褐孔菌的定量分析和质量评价提供科学的依据。 相似文献
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Lead levels in different environmental media (soil, grass leaves, water, ceramics, pencil, paint, crayons and cosmetics) were determined to assess the major sources of lead exposure in Thohoyandou, South Africa. Soil and plant leaves were used as indicators of Pb pollution from vehicle exhaust emissions. After digestion with concentrated acids (HNO3, HCl and HClO4) Pb concentrations were determined in triplicate using a flame atomic absorption spectrometer. The mean Pb concentrations at the kerb of selected busy roads were 205.5 ± 90, 273.0 ± 90 and 312.8 ± 81 μg g−1 and 154.7 ± 67, 182.9 ± 76 and 240.6 ± 66 μg g−1 for soil and plant leaves (dry weight) respectively. These concentrations were substantially higher than the values found on soils 50 m away from the roads (97.4 ± 11 μg g−1). Pb concentrations in plants collected further away from the road (50 m) were substantially lower (71.8 ± 9.0 μg g−1). The observed levels on soil are lower than the UK critical value of 500 μg g−1 for gardens and allotments; and 2000 μg g−1 for parks and open space as well as the Canadian values for agricultural (375 μg g−1), residential (500 μg g−1 and industrial (1000 μg g−1). From these data it was clear that Pb concentrations in soil samples were substantially higher than the levels obtained for plant leaves. The Pb levels in green crayons, blue crayons, pencils (from China & Germany), were 10650 ± 75.2, 8200 ± 52.4, 1160 ± 50.2, 79 ± 10.1 μg g−1 for the inner contents; and 4870 ± 58.1, 5650 ± 55.5, 1950 ± 46.6, 60 ± 12.9 μg g−1 for the outer surface paint respectively. The ceramics showed Pb levels of 630 ± 50.3 μg g−1 (saucer) and 560 ± 32.2 μg g−1 (cup), while the inner contents and outer surface paint showed 480 ± 32.4 and 318 ± 21.2 μg g−1 of Pb respectively. Early morning tap water flush gave a Pb level of 20.6 ± 5.6 μg Pb l−1. This value is higher than the WHO and FDA maximum permissible concentrations of 10 μg l−1 and 15 μg l−1 respectively. 相似文献
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实验研究了NaCl改性沸石去除水中铅的效果,比较了沸石改性前后对铅的静态平衡吸附量变化,着重考察了吸附时间、pH值、竞争离子以及有机物对去除铅效果的影响。结果表明:NaCl改性沸石吸附铅速度快,对铅有很好的去除效果,平衡吸附量由改性前的28.57mg/g提高到了32.26mg/g。pH值对NaCl改性沸石去除水中铅的效果有较大影响,在pH=6~7时,去除效果最佳。水中竞争阳离子和有机物的存在,在一定程度上会降低铅的去除效果;随干扰物质浓度的升高,NaCl改性沸石对铅去除率出现了明显的下降,但当干扰物质和水样中铅浓度相当时,NaCl改性沸石可对铅保持很高的去除率。 相似文献
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Lead removal from contaminated water using mineral adsorbents 总被引:3,自引:0,他引:3
M. N. Rashed 《The Environmentalist》2001,21(3):187-195
This study records experiments undertaken to determine the suitable conditions for the use of naturally occurring minerals (talc, chalcopyrite and barite) as an adsorbent for the removal of lead ions from liquid wastes. The adsorption of lead ions from solutions containing different initial lead concentrations (50, 100, 200, 400, 600, 800 and 1000 mg l–1 Pb as lead nitrate) using different size fractions (<63 m, 63–150 m) of talc, chalcopyrite and barite at different pH (3, 5, 7 and 9) and different adsorption times (24, 48, 72 and 96 hr) was examined. The results revealed that of the studied minerals, the chalcopyrite fraction at 63–150 m showed the highest adsorption capacity. The adsorption data of Pb ions was also analyzed with the help of the Langmuir and Freundlich models to evaluate the mechanistic parameters associated with the adsorption process. The adsorption isotherms obtained from the Langmuir and Freundlich equations were generally linear and the adsorption of Pb by the studied minerals was correlated with the adsorption maximum and binding energy constant of the Langmuir equation and equilibrium partition constant and binding partition coefficient of the Freundlich equation. It was concluded that the equilibrium time of adsorption was 72 hr at an optimum pH from 7 to 9. This technique might be successfully used for the removal of lead ions from liquid industrial wastes and wastewater. 相似文献
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目前测定铅的分析方法主要有分光光度法、阳极溶出伏安法、示波极谱法、原子吸收法等。针对比色法灵敏度低,试剂不稳定;电化学法干扰严重;而原子吸收法,线性范围窄,样品用量大等问题,江苏油田采用氢化物发生原子荧光法测定钻井废水中的铅。样品经HNO3-HClO4消解,3%~4%KBH4还原,以0.8%~1.5%的HCl为介质,加入10%K3Fe(CN)6和2%H2C2O4基体改进剂,用原子荧光法连续测定钻井废水中的铅。铅的检测限为0.61ng/mL,回收率为87.4%~146%,变异系数<4.2%。该方法操作简单,灵敏度高。 相似文献
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Lead concentrations were determined for particulates which were deposited during one year on the leaves of roadside plants in Karachi. The particulates were collected from the leaves at a height of one metre. The lead accumulated by the leaves of different species was also measured. A statistically significant correlation was found between the number of passing petrol driven vehicles and the lead concentration in the deposits at different designated sites. However, no significant correlation was found between the concentration in the deposits and the lead accumulated by the leaves. A lead concentration of 30.00±6.6 ppm was recorded as the highest concentration in the particulate deposits, while maximum lead accumulated by the leaves was noted as 3.12±1.09 ppm. 相似文献
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用萃取火焰AAS法测定汽车道旁树叶中的铅含量 总被引:4,自引:0,他引:4
主要介绍了用碘化钾-甲基异丁基甲酮(KI-MIBK)萃取汽车道旁植物叶片中的微量铅,然后用原子吸收分光光度法(AAS)测定,该方法的精密度和准确度均有较满意的结果 相似文献
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近年来,铅蓄电池行业铅污染事故频发,对环境和人体健康造成了严重危害。各级政府高度重视,环境保护部于2011年初开展铅蓄电池行业环保专项检查工作。本文从铅蓄电池行业的生产全过程出发,从产业结构、技术装备、末端治理、环境管理等方面提出铅蓄电池行业铅污染防治措施,为铅蓄电池行业重金属污染防治工作提供了参考依据。 相似文献