青岛酸雨天气边界层气象特征

青岛地区酸雨成因研究表明,青岛市近代工业发展排放大量致酸物质、海洋上天然排放的二甲基硫是重要的原因;青岛地区边界层风场和温度场的特殊规律是形成酸雨的另一个重要原因;江淮气旋和黄淮气旋大型天气形势起了辅助作用。本文着重分析研究了1993年7月23日一次典型酸雨的实际例子,证明了上述论点。     

胡敏酸在土壤中的迁移

研究了不同条件下胡敏酸在土壤中的迁移过程.结果表明,其迁移过程表现出较大的差异,在溶液pH值、胡敏酸浓度和溶液流速均较高时,胡敏酸迁移的阻滞因子和在土壤中的吸附系数均较低,有利于胡敏酸在土壤中的迁移;在溶液pH值、胡敏酸浓度和溶液流速均较低时,土壤对胡敏酸迁移的阻滞作用较大.胡敏酸的迁移还与土壤性质有关,土壤黏粒含量和阳离子交换量越高,胡敏酸在土壤中吸附的越多,越不利于迁移.在土壤中的吸附是胡敏酸迁移的主要控制因素,在预测胡敏酸在水土环境中迁移时,应该充分考虑不同条件下胡敏酸在不同性质土壤中的吸附.     

沈阳市降雪中PFOS和PFOA污染现状调查

通过调查降雪中PFOS和PFOA的浓度,阐明了沈阳市大气中PFOS和PFOA的污染状况和污染规律.2006-02-06采集沈阳市区和郊区共计36个采样点的降雪样品,2006-02-25在其中5个采样点再次采集降雪样品.固相萃取融雪水中的PFOS和PFOA,利用LC-MS-SIM法测定样品中PFOS和PFOA浓度.全部样品中均检出PFOS和PFOA.2006-02-06降雪中PFOS和PFOA的浓度几何平均值分别为2.0 ng·L^-1（范围：0.4～46.2 ng·L^-1）和3.6 ng·L^-1（范围：1.6～22.4 ng·L^-1）,95%置信区间分别为1.5～2.8 ng·L^-1和3.1～4.2 ng·L^-1.PFOS和PFOA的最高浓度同时出现在郊区采样点朱尔屯,市中心区2种物质的浓度呈显著正相关.2006-02-25的5个采样点降雪中PFOS和PFOA的浓度几何平均值均为2.2 ng·L^-1.2次降雪中PFOS浓度差异不显著,2006-02-25降雪中PFOA浓度高于2006-02-06.结果表明,沈阳市区和郊区降雪中广泛存在PFOS和PFOA污染,局部区域可能存在共同的PFOS和PFOA污染来源;沈阳地区有较稳定的PFOS来源持续向大气中输送该类物质;PFOS和PFOA的环境行为可能不同.     

Co-transport of dissolved organic matter and heavy metals in soils induced by excessive phosphorus applications

To evaluate the e ects of long-term applications of phosphorus fertilizers on mobility of dissolved organic matter (DOM) and heavy metals in agricultural soils, a sandy soil and a loamy soil were spiked with ammonium phosphate at application rates of 0, 25, 50, 100, 250, and 500 mg P per kilogram of soil. A series of 15-cm long soil columns were constructed by packing incubated soils of varying concentrations of P. The soil columns were consecutively leached by simulated rainfalls for six cycles. The contents of water extractable organic carbon in both sandy and loamy soils increased significantly with increasing rates of P applications. Relatively high rates of P applications could induce a marked increase in DOM concentrations in the leachates, the e ects were larger with the sandy soil rather than with the loamy soil. Applications of P changed the partitioning of trace metals in the soil solids and the soil solutions. The increased P application rates also seemed to elevate the leaching of Cu, Cd, and Zn from soils. The concentrations of Cu, Cd, and Zn in the leachates were positively correlated with DOM, probably due to the formation of metal-DOM complexes. In contrast, Pb concentrations in the leachates were negatively correlated with DOM, and decreased with increasing rates of P applications. The boosted leaching of DOM induced by high rates of P applications was probably due to the added phosphate ions competing for adsorption sites in the soil solids with the indigenous DOM.     

覆膜与降雨类型对土壤水分及NO3--N淋失的影响

在丹江口库区青塘河五龙池小流域,以黄棕壤横垄种植玉米为例,设置覆膜与无覆膜两种处理,采用田间小区实验研究覆膜与降雨类型对0~30 cm土壤水分和NO-3-N淋失的影响.结果表明:两处理土壤含水量均随土层加深而增加,与无覆膜相比覆膜可降低0~10、10~20、20~30cm土层中的含水量.不同降雨类型对覆膜土壤含水量的影响有区别,小雨时3层土壤间差异显著,含水量随土层加深急剧增加;中雨时10~20cm比0~10 cm、20~30 cm比10~20 cm分别高50.80%、6.62%,0~10 cm土壤含水量显著低于10~20 cm和20~30 cm;暴雨时含水量随土层加深增幅变小;覆膜土壤土层越深土壤含水量受降雨的影响越小.覆膜可降低0~10、10~20 cm土层中的NO-3-N淋失量,分别降低40.74%、24.48%,但会增加20~30 cm的淋失;两处理土壤NO-3-N淋失量均随土层加深而增加.不同降雨类型对覆膜土壤NO-3-N淋失的影响也有区别,小雨时随土壤深度的增加淋失量增多;中雨时,0~10、20~30 cm NO-3-N淋失量分别为10~20 cm的1.75、8.41倍;暴雨时,0~10、20~30 cm分别比10~20 cm低18.97%和60.69%.土壤中NO-3-N淋失受土壤含水量的影响,且随土层加深含水量对NO-3-N淋失的影响减弱.     

二级SBR系统处理染料废水长期运行的稳定性

考察了处理染料废水的二级SBR系统在连续运行120个周期过程中的稳定性.系统的运行先后经历了低染料浓度和高染料浓度2种情况.试验发现在长期运行过程中,二级SBR系统对进水水质及操作条件具有良好的适应性;能够有效去除废水中的污染物,对染料的平均去除率为81%～92.5%,对COD的平均去除率为89.4%～93.1%;出水水质比较稳定.在二级SBR系统中,厌氧污泥活性高,降解污染物能力强;好氧活性污泥形成团簇状结构,有利于稳定出水水质.     

土壤风化速率的实验测定

利用模拟淋溶实验测定了中国几种土壤（砖红壤，赤红壤，红壤，黄棕壤和紫色土）的风化速率，并研究了土壤pH值和降水量对土壤风化速度的影响，结果表明，土壤的风化速度在pH≥4时随pH值的下降而显著增加，但是当pH值低于4时，风化速率却急剧下降，造成这种现象的原因可能是在低pH值时盐基阳离子和铝离子大量溶出，过高的产物浓度限制了风化反应的进行。土壤的风化速度与淋溶速率之间近似成线性关系。用淋溶液pH值和淋溶液量两个因素对实验结果进行了校正。     

滇池流域土壤活性腐殖质及其主要组分的紫外-可见与三维荧光光学特性

利用紫外-可见光谱和三维荧光光谱技术,结合土壤腐殖质及腐殖质组分(胡敏酸、富里酸)中的有机碳含量,研究了滇池流域土壤活性腐殖质及其组分胡敏酸和富里酸的光谱特征.结果表明,滇池流域土壤活性腐殖质中富里酸含量高于胡敏酸,流域范围内土壤活性腐殖质及其组分含量分布不均匀,活性腐殖质、胡敏酸和富里酸含量的变异系数分别达37.7%、36.4%、40.9%.土壤活性腐殖质及其组分胡敏酸和富里酸的碳含量均表现为菜地荒地草地湿地.光谱特征结果表明,滇池流域土壤活性腐殖质主要由自生源物质和经一定程度降解后的外源物质共同组成.此外,自生源性与光化学及生物活性具有正相关关系.因此,具有弱自生源性的滇池流域土壤活性腐殖质所具有的光化学和生物活性较弱.     

华南地区高山酸沉降化学研究

1987—1989年春季,在华南地区衡山、狮子山、苗儿山和白云山观测到华南高山降水酸化,各测点降水pH<5.6的频率大于68％,平均pH值在3.56—4.85之间,分析了高山降水的化学特征,及其与高山的地理环境等因素的关系.结果表明,高山雨水与高空云水有相似性,狮子山和白云山的云雾水主要属地形云,受局地源的影响更为严重,化学性质更接近于地面雨水.     

Efficient adsorption of Mn(Ⅱ) by layered double hydroxides intercalated with diethylenetriaminepentaacetic acid and the mechanistic study

In this study, greatly enhanced Mn(II) adsorption was achieved by as-synthesized diethylenetriaminepentaacetate acid intercalated Mg/Al layered double hydroxides(LDHsDTPA). The adsorption capacity of LDHs-DTPA was 83.5 mg/g, which is much higher than that of LDHs-EDTA(44.4 mg/g), LDHs-Oxalate(21.6 mg/g) and LDHs(28.8 mg/g). The adsorption data of aqueous Mn(II) using LDHs-DTPA could be well described by the pseudosecond order kinetics and Langmuir isotherm model. Thermodynamics study results also showed that the adsorption process of Mn(II) by LDHs-DTPA was exothermic as indicated by the negative ΔH value. Furthermore, based on the structural, morphological and thermostable features, as well as FT-IR and XPS characterizations of LDHs-DTPA and the pristine LDHs, the adsorption mechanism of Mn(II) was proposed. The carboxyl groups of DTPA were proposed to be the main binding sites for Mn(II), and the hydroxyl groups of LDHs also played a minor role in the adsorption process. Among the three common regeneration reagents, 0.1 mol/L Na_2CO_3 was the best for reusing LDHs-DTPA in Mn(II)adsorption. Besides, the Mn(II) adsorption performance could be hindered in the presence of typical inorganic ions, especially cations. Further specific modifications of LDHs-DTPA are suggested to get more selective adsorption of Mn(II) in practical applications.