磷酸铵镁沉淀法脱除生活污水中氮磷的研究

针对低有机物高氨氮浓度的生活污水,经UASB处理后的厌氧废水,氮含量较高,磷基本未除去,处理出水效果欠佳的情况,提出磷酸铵铗沉淀法脱除生活污水中的磷以及部分氨氮。初步确定了影响磷酸铵镁沉淀反应因素为pH值,Mg^2＋：PO4^3-：NH4^＋,反应时间t。最优反应条件为：pH=8．5,Mg^2＋：PO4^3-：NH4^＋=1．2：1：1,反应时间t=1min。磷的去除率可高达94．0％,氨氮的去除率达71．5％,为低浓度的生活污水的后续生物处理创造了良好的条件。     

桑沟湾养殖水域表层沉积物对磷酸盐的吸附特征

在室内模拟扰动条件下,研究了桑沟湾养殖水域表层沉积物对磷酸盐的吸附动力学及其吸附等温线,探讨了磷酸盐的吸附-解吸平衡质量浓度以及沉积物的源汇角色.结果表明,沉积物对磷酸盐的吸附主要发生在0～0.5 h,吸附平衡时间约为6 h,吸附动力学方程符合修正的Elovich模型,回归方程为： Q =85.536+35.512 ln t （r²=0.960 2）;低浓度条件下沉积物对磷酸盐的吸附等温线呈线性,线性方程为： Q =265.04 c _e-7.46（ Ｒ ²=0.965）,高浓度条件下沉积物对磷酸盐的吸附等温线符合Langmuir模型（ Ｒ ²=0.989）;沉积物中本底吸附态磷为7.46 μg/g,对磷的最大吸附量 Ｑ _max为769.23 μg/g;沉积物对磷酸盐的吸附-解吸平衡质量浓度EPC₀为0.028 mg/L,结合该区域水体磷酸盐含量情况,初步推断该区域的沉积物大多数时间充当的是磷源的角色.     

互花米草对持续淹水胁迫的生理响应

对互花米草进行了40cm水深的持续淹水胁迫,研究了其生理指标的响应.结果显示,淹水胁迫下,互花米草叶片中可溶性糖含量和叶绿索含量在初期均显著低于对照,随后逐渐积累并高于对照.丙二醛含量在初期显著高于对照,随后与对照组的差异逐渐减小,至生长季末与对照水平相当.过氧化物酶活性在淹水后63d内均高于对照,至生长季末则低于对照,而超氧化物歧化酶活性则始终高于对照.至生长季末,持续淹水胁迫条件下的互花米草生物量低于对照,其形态学上表现为植株矮小、根系变短、节长变短、地下部分所占生物量比重降低.研究结果表明,持续淹水胁迫对互花米草的生理指标产生影响,但互花米草可以通过生理和形态学的响应来适应这种胁迫,因此,必须进一步结合其它物理控制措施进行综合治理.     

不同物质对亚硝酸盐积累的影响

亚硝化-厌氧氨氧化脱氮工艺的关键是实现亚硝酸盐的累积.实验采用SBR反应器,在实现亚硝酸盐稳定积累的基础上.考察了不同的碳源种类及离子对亚硝酸盐积累的影响.结果表明,当进水COD不高于200mg·L-1(0磷酸盐>氯离子>C/N.     

应用物种敏感性分布评估DDT和林丹对淡水生物的生态风险

介绍了利用物种敏感性分布（SSD）进行生态风险评价的原理与步骤,构建了淡水生物对DDT和林丹的物种敏感性分布.在此基础上,计算了DDT和林丹对不同类别生物的HC5(Hazardous Concentration for 5% the species)阈值,预测了不同浓度DDT和林丹对生物可能造成的危害,并比较了不同类别生物对DDT和林丹的敏感性,以及DDT和林丹对淡水生物的生态风险.结果表明,DDT和林丹对淡水生物的HC5值分别为1.70μg·L-1和5.96μg·L-1 ,DDT对生态系统的危害大于林丹.当DDT或林丹的浓度为5μg·L-1时,对生态系统仅有轻微影响,而当DDT或林丹的浓度为500μg·L-1时,将有81.5%的物种受到DDT的危害,或有68.1%的物种受到林丹的危害.不同类别生物对DDT的敏感性从甲壳类、昆虫和蜘蛛类到鱼类依次降低,对林丹的敏感性大小依次为昆虫和蜘蛛类、甲壳类、鱼类.与林丹相比,DDT对淡水脊椎动物与无脊椎动物以及甲壳类和鱼类的生态风险较大,而对昆虫和蜘蛛类,林丹与DDT的生态风险差别不大.     

Preparation of high concentration polyaluminum chloride with high content of Alb or Alc

A novel membrane distillation concentration method was used to prepare high concentration polyaluminum chloride (PACl) with high content of Al_b or Al_c. 2.52 mol/L PACl₁ with 88% Al_b and 2.38 mol/L PACl₂ with 61% Al_c were successfully prepared. Three coagulants, AlCl₃, PACl₁ and PACl₂ were investigated on their hydrolysis behavior and speciation under different conditions. The effects of pH and dilution ratio on Al species distribution were investigated by ferron assay. Experimental result showed that pH had a significant effect on Al species distribution for the three coagulants. Dilution ratio had little effects on Al_b and Al_c distribution in whole dilution process except the beginning for PACl₁ and PACl₂. The results indicated that transformation of Al depends largely on their original composition. AlCl₃ was the most unstable coagulant among these three coagulants during hydrolysis process. PACl₁ and PACl₂ with significant amounts of highly charged and stable polynuclear aluminum hydrolysis products were less affected by the hydrolysis conditions and could maintain high speciation stability under various conditions.     

Simultaneous oxidation of NO, SO2 and Hg0 from flue gas by pulsed corona discharge

A process capable of oxidizing NO, SO2 and Hg0 was proposed simultaneously, which utilized a high-voltage and short-duration positive pulsed corona discharge. By focusing on NO, SO2, and Hg0 oxidation efficiencies, the influences of pulse peak voltage, pulse frequency, initial concentration, electrode number, residence time and water vapor addition were investigated. The results indicate that NO, SO2 and Hg0 oxidation efficiencies depend primarily on the radicals (OH, HO2, O) and the active species (O3, H2O2), etc. produced by the pulsed corona discharge. The NO, SO2 and Hg0 oxidation efficiencies improved as increasing pulse peak voltage, pulse frequency, electrode number and residence time, while they are reduced with an increasing initial concentration. By adding water vapor, SO2 oxidation efficiency is improved remarkably, while NO oxidation efficiency is decreased slightly. In our experiments, the simultaneous NO, SO2, and Hg0 oxidation efficiencies reached to 40%, 98% and 55% with the initial concentrations 479 mg/m3, 1040 mg/m3, and 15.0 ug/m3, respectively.     

酚类污染物解离态与非解离态光解特性及其速率常数的预测

以氙灯为光源模拟太阳光,通过研究不同pH条件下3种酚类污染物直接光解的过程,探讨了酚类污染物的解离对其光解规律的影响,并建立了解离态与非解离态酚类污染物光解速率常数的计算方法及预测模式.结果表明,随着pH从4.0增加到9.0,五氯酚的光解速率常数随之从25.30×10-4min-1增加到82.90×10-4min-1,而对硝基酚的光解速率常数相应从11.90×10-4min-1降低到了3.18×10-4min-1.苯酚的光解趋势与对硝基酚相似,当pH从4.0增加到11.0时,其光解速率常数依次从32.50×10-4min-1降低至13.40×10-4min-1.3种酚类化合物的光解总速率常数与解离度之间均满足幂函数变化规律.任意解离度条件下的解离态和非解离态光解速率常数,可根据幂函数的切线方程来确定.解离对酚类物质降解规律的影响主要是通过氧负离子的形成,改变苯环以及其他取代基团的活性而造成的.该研究结果为进一步了解天然水环境中酚类污染物的环境行为提供了理论参考.     

Temporal variability of iron concentrations and fractions in wetland waters in Sanjiang Plain, Northeast China

Chemical forms, reactivities and transformation of iron fractions in marshy waters were investigated with cross-flow filtration technique to study the iron environmental behavior. Iron fractions were divided into four parts: acid-labile iron (pre-acidification of unfiltered marshy water samples, 0.7 μm), high-molecular-weight iron (0.7-0.05 μm), medium-molecular-weight iron (0.05-0.01 μm), and low-molecular-weight iron ( 0.01 μm). The cross-flow filtration suggested that iron primarily exist in both the 0.7 μm and 0.01 μm size fractions in marshy waters. Rainfall is the key for rain-fed wetland to determine fate of iron by changing the aquatic biochemical conditions. By monitoring the variation of iron concentrations and fractions over three years, it was found that dissolved iron and acid-labile iron concentrations exhibit a large variation extent under different annual rainfalls from 2006 to 2008. The seasonal variation for iron species proved that the surface temperature could control some conversion reactions of iron in marshy waters. Low- molecular-weight iron would convert to acid-labile iron gradually with temperature decreasing. The photochemical reactions of iron fractions, especially low-molecular-weight iron had occurred under solar irradiation. The relative proportion of low-molecular-weight in total dissolved iron ranging from 28.3% to 43.2% were found during the day time, which proved that the observed decreasing concentration of acid lability iron was caused by its degradation to low molecular weight iron.     

不同养分对磷酸盐固定的污染土壤中铜锌生物有效性的影响

采用盆栽试验,在磷酸盐固定铜、锌单一及复合的三级污染(Cu 200 mg·kg^-1、Zn 400 mg·kg^-1)红壤和水稻土中,种植黑麦草40　d,测定不加养分、加入KCl和NH₄Cl、K₂SO₄和(NH₄)₂SO₄后土壤中有效态铜锌含量、黑麦草生物量及其铜锌吸收量,以讨论养分对污染土壤中磷酸盐固定态铜锌的活化作用.结果表明,磷酸盐固定的铜单一、锌单一和铜锌复合污染红壤中,增加养分,有效态铜锌的含量都较未加入养分的增高,并且养分KCl和NH₄Cl的增高幅度大于K₂SO₄和(NH₄)₂SO₄,其中在磷酸盐固定的锌单一污染红壤中,有效态锌含量较未加入养分时增幅高达133.4%.虽然加入K₂SO₄和(NH₄)₂SO₄,促进了红壤中黑麦草植株的生长,最大增幅达22.2%,但同时也增加了植株21.5%～112.6%的铜锌吸收量.调节养分对水稻土中铜锌的生物有效性没有显著影响.施入氮钾等养分能够改变磷酸盐固定的污染红壤中铜锌的生物有效性,对固定的铜锌都有活化作用.因此,在重金属污染土壤的修复中要充分考虑施肥等养分条件对固定钝化的重金属活性的影响.