化工生化尾水中溶解性有机污染物的富集分离

采用液液萃取法和树脂吸附法对化工园区的生化尾水中溶解性有机污染物进行富集、分离,通过气相色谱-质谱分析表明化工生化尾水中普遍含有四氯乙烯、苯类和烷烃类有机毒物,而不同来源的化工生化尾水中疏水性、亲水性和中性有机质的含量相差较大,分子量分布也不相同,液相色谱-质谱分析表明树脂富集分离后,氨基酸、邻苯二甲酸酯和糖类物质成为尾水中主要有机物。     

浅议攀钢翻渣场污染物无害化治理措施

针对攀钢在钢铁生产过程中产生的大量冶炼废弃物,主要是固、液、粉尘三类污染物,分别采用挡渣坝、挡水坝和喷洒降尘进行了处理,从而降低了污染物的扩散,实现了无害化的治理。     

氧化剂对土壤中石油污染物去除率的影响

以FeSO_4-柠檬酸为催化剂,探讨了不同氧化剂的类型、浓度、与催化剂的比例等因素对土壤中石油污染物去除率的影响。实验结果表明:各氧化剂体系的石油去除率大小顺序为KMnO_4CaO_2≥H_2O_2K_2S_2O_8;随着反应时间的延长,各体系的石油去除率均呈现出先快速增涨、再缓慢增加后略有降低的趋势;在氧化剂浓度相同条件下,H_2O_2体系和Na_2S_2O_8体系的石油去除率分别比对照增加了145.5%~238.7%和112.6%~167.5%;在催化剂用量相同条件下,H_2O_2体系和Na_2S_2O_8体系达到最高石油去除率时的n(氧化剂)∶n(催化剂)分别为50∶1和100∶1;H_2O_2体系对残油族组分的去除率大小顺序为非烃芳烃饱和烃沥青质。     

Stomatal uptake of O3 in aspen and aspen-birch forests under free-air CO2 and O3 enrichment

Rising atmospheric carbon dioxide (CO₂) may alleviate the toxicological impacts of concurrently rising tropospheric ozone (O₃) during the present century if higher CO₂ is accompanied by lower stomatal conductance (g_s), as assumed by many models. We investigated how elevated concentrations of CO₂ and O₃, alone and in combination, affected the accumulated stomatal flux of O₃ (AFst) by canopies and sun leaves in closed aspen and aspen-birch forests in the free-air CO₂-O₃ enrichment experiment near Rhinelander, Wisconsin. Stomatal conductance for O₃ was derived from sap flux data and AFst was estimated either neglecting or accounting for the potential influence of non-stomatal leaf surface O₃ deposition. Leaf-level AFst (AFst_l) was not reduced by elevated CO₂. Instead, there was a significant CO₂ × O₃ interaction on AFst_l, as a consequence of lower values of g_s in control plots and the combination treatment than in the two single-gas treatments. In addition, aspen leaves had higher AFst_l than birch leaves, and estimates of AFst_l were not very sensitive to non-stomatal leaf surface O₃ deposition. Our results suggest that model projections of large CO₂-induced reductions in g_s alleviating the adverse effect of rising tropospheric O₃ may not be reasonable for northern hardwood forests.     

致癌和非致癌环境健康风险的预期寿命损失评价法

预期寿命损失法（loss of life expectancy,LLE）可以对致癌和非致癌物质的环境健康风险进行评价和比较,是一种污染物环境健康风险评价的新方法.应用该方法对中国目前危害较大的6种典型致癌和非致癌污染物砷、DDTs、苯并芘、铅、汞、镉造成的人体的预期寿命损失进行了分析,并比较了6种污染物的环境健康风险大小.结果表明,预期寿命损失法可以作为污染物健康风险评价的一种方法,致癌物质砷、DDTs、苯并芘分别导致一个健康个体寿命损失3.6 d、2.2 d和12.1 d,非致癌物质铅、汞、镉分别导致一个健康个体寿命损失1.1 d、1.7 d和5.8 d;用预期寿命损失方法可以对致癌、非致癌风险在同一尺度上进行比较,在目标污染物现有相关研究基础上,6种污染物的健康风险大小顺序为苯并芘＞镉＞砷＞DDTs＞汞＞铅.     

持续性降水气象条件下土壤/大气间汞通量特征

为研究自然条件下地表大气间汞交换通量特征及其影响因素,2012年4月22~25日在位于松花江上游的夹皮沟金矿,使用动态通量箱法(dynamic flux chamber, DFC)与汞分析仪(LUMEX Zeeman RA915+)联用技术测定了在持续性降雨气象条件控制下矿区土壤大气间汞交换通量,同步测定了近地面垂向0~150cm范围内大气汞浓度以及太阳辐射强度和大气温湿度,并分析了汞交换通量与降水条件下气象因子间相关关系.结果表明:在持续性降雨条件控制下,地表大气间的汞交换通量表现为沉降与释放过程连续交替出现特征,这与晴朗天气条件下日型汞通量单峰结构明显不同.降水间歇期土壤大气间汞交换通量在坡耕农田采样点依次为(-2.08±6.11)、(-6.16±33.57)、(-3.20±8.64)和(5.06±18.80)ng/(m2·h);在谷底漫滩采样点依次为(-5.21±6.42)、(3.87±28.12)、(-11.87±14.10)和(-9.44±12.23)ng/(m2·h).在局地范围内,地形条件差异影响不同地表和近地面大气系统能量收支,并使近地面大气汞浓度和气象因子发生变化,进而影响地表大气间汞交换通量过程和水平.持续性降水条件下,地表和大气间汞交换通量与太阳辐射强度和大气湿度间具有较为明显的正线性相关关系,与大气汞浓度和大气温度间无明显线性相关关系.     

β-FeOOH/蜂窝陶瓷催化臭氧化高效去除饮用水中有机污染物

市售蜂窝陶瓷经过氧化铝涂层后,进一步负载β-FeOOH活性组分,制得改性蜂窝陶瓷催化剂(β-FeOOH/Ce-ramic honeycomb,β-FeOOH/CH)。与单独臭氧氧化相比,基于该催化剂的固定床反应装置体现出更好的臭氧化活性,反应20 min后,水中的2,4-二氯苯氧乙酸(2,4-D)就可以完全去除,其矿化效率也可以达到80%以上。进一步考察了进水流速、有机物浓度等因素对多相催化臭氧化效率的影响,结果表明:β-FeOOH/CH可以显著提高臭氧的利用效率,能够有效去除水中包括2,4-D在内的多种有机污染物,而且催化剂可以重复使用,在长期的运行实验中其催化性能没有明显下降,该反应装置在饮用水深度处理领域具有很好的应用潜力。     

海南昌江石碌钴铜矿尾矿库重金属污染环境现状调查

为了解海南省昌江县石碌镇钴铜矿尾矿库环境特点,分别采集了矿砂、背景土壤、废水、纳污水体和植物进行分析。结果表明,钴铜矿尾矿库的土壤受As和Cu污染严重,周边土壤受到不同程度的重金属污染;废水经过尾矿库沉淀处理后,SS、As、Cu、Co、Fe等监测指标均有所降低,尾矿库起到沉淀吸附处理作用;纳污河流石碌河水质良好;尾矿库内自然生长的菖蒲和水竹均受到重金属不同程度污染,尾矿库内的甘蔗中Cr、Pb含量均超过食品中污染物限量标准,表明尾矿库内不宜种植可食用作物。     

我国轻型汽车污染物排放因子的测试研究

采用底盘测功机按ＥＣＥ－１５规程测试了我国１３辆（１２种）正在使用的轻型汽车的ＣＯ、ＨＣ和ＮＯｘ的排放量分别为８７．２５±５６．３１、１１．３６±５．１３和８．２０±６．６８ｇ／ｔｅｓｔ;在相同测试条件下,测试了其中１１种轻型车在不同车速匀速行驶时的ＣＯ、ＨＣ和ＮＯｘ排放因子．测试结果表明、轻型汽车污染物排放因子随车速的变化有良好的规律性．用统计方法拟合了轻型汽车污染物排放因子的车速变化系数的计算公式。当车速＜９０ｋｍ／ｈ时,轻型车ＣＯ、ＨＣ排放因子随车速的增加而减小,当车速＞９０ｋｍ／ｈ时,又略有增加,而ＮＯｘ排放因子随车速的增加而增大。     

Effect of organic matter and pH on mercury release from soils

An investigation was conducted on the effect of organic matter(OM)and pH on mercury(Hg)release from soils.Hg release flux was measured using the dynamic flux chamber(DFC)combined with the Lumex multifunctional mercury analyzer in both laboratory experiment and field monitoring.The results showed that Hg emission from the OM-added soils was apparently low because of the high affinity of OM to Hg,resulting in the reverse order as the amount of OM addition.Meanwhile,Hg release flux from different pH value soils exhibited the same trend for both Hg~(2 )and Hg_2~(2 )treatment,increasing the Hg flux with pH value of soils increasing.The trend of Hg release in the pH dependence experiment has been well in agreement with that from the field test.In addition,Hg release seemed to be related to its species in the soil,the flux from Hg~(2 )-added soil was obviously higher than that of Hg_2~(2 )-added soil by the laboratory experiment.