阳离子絮凝剂P(AM-DAC)的合成、表征及应用

以丙烯酰胺(AM)和丙烯酰氧乙基三甲基氯化铵(DAC)为单体,过硫酸钾(KPS)为引发剂,通过水溶液聚合的方法合成了阳离子絮凝剂P(AM-DAC)。探讨了单体配比、单体浓度、引发剂用量、反应时间、反应温度等因素对阳离子聚丙烯酰胺(CPAM)主要性能的影响。实验得出了较佳的反应条件:聚合温度为70℃,引发剂用量为0.16%,单体配比m(AM):m(DAC)=1:8,总单体浓度为20%,反应时间3 h。在上述条件下,所得阳离子聚丙烯酰胺絮凝剂的特性黏数为18.692 4 dL/g,在其加入量为0.003%的条件下处理巡司河污水,上层清液透光率达90.7%,污泥脱水率达89.2%。并对该聚合物絮凝剂的结构和热行为进行了表征。     

污染河口区沉积物-水界面营养盐交换通量的实验研究

采集青岛市李村河口下游沉积物柱状样品,通过实验室培养实验,研究了溶解氧、温度、盐度、生物扰动等环境因素对沉积物-水界面营养盐交换通量的影响。结果表明,NO3-N、NH4-N、PO4-P在贫氧环境下的交换通量要高于富氧条件下,NO2-N受溶解氧含量的影响较小;随着温度的升高,NO3-N、NH4-N、PO4-P的交换通量增大,而NO2-N的交换通量减小;NO2-N和NH4-N的交换通量随盐度增大而增大,NO3-N减小,而PO4-P受盐度的影响较小;生物扰动对营养盐在沉积物-水界面的交换通量的影响显著。     

Production and contribution of hydroxyl radicals between the DSA anode and water interface

Hydroxyl radicals play the key role during electrochemical oxidation and photoelectrochemical oxidation. The production and e ect of hydroxyl radicals on the interface between DSA anode and water was investigated by examining the quenching e ect of iso-propanol on Orange II decolorization. We observed that with an increase in electrode potential from 4 to 12 V across electrodes at pH 7.0, the contribution percentage of hydroxyl radicals increased dramatically. More OH radicals were produced in acidic and alkaline conditions than at neutral conditions. At electrode potential of 4 V, the contribution percentage of hydroxyl radicals was obviously higher at near neutral pH conditions, while removal e ciency of Orange II achieved was the lowest concurrently. Finally, for photocatalytic oxidation, electrochemical oxidation, and photoelectrochemical oxidation using the same DSA electrode, the e ect of hydroxyl radicals proved to be dominant in photocatalytic oxidation but the contribution of hydroxyl radicals was not dominant in electrochemical oxidation, which implies the necessity of UV irradiation for electrochemical oxidation during water treatment.     

Effects of overlying water aeration on phosphorus fractions and alkaline phosphatase activity in surface sediment

Microbial activity may influence phosphorus (P) deposit and release at the water sediment interface. The properties of DO (dissolved oxygen), pH, P fractions (TP, Ca-P, Fe-P, OP, IP), and APA (alkaline phosphatase activity) at the water sediment interface were measured to investigate microbial activity variations in surface sediment under conditions of two-month intermittent aeration in overlying water. Results showed that DO and TP of overlying water increased rapidly in the first week and then decreased gradually after 15 day of intermittent aeration. Microorganism metabolism in surface sediment increased pH and decreased DO and TP in the overlying water. After two-month intermittent aeration, APA and OP from surface sediment (0–2 cm) were both significantly higher than those from bottom sediment (6–8 cm) (p < 0.05), and surface sediment Fe-P was transferred to OP during the course of microorganism reproduction on the surface sediment. These results suggest that microbial activity and microorganism biomass from the surface sediment were higher than those from bottom sediment after two-month intermittent aeration in the overlying water.     

霍甫水丝蚓对太湖梅梁湾沉积物影响——水界面无机氮、磷交换

根据太湖梅梁湾大型底柄动物的自然分布特征,运用沉积物-水微宇宙的实验方法评估了霍甫水丝蚓(Limnodrilus hoffmeristeri)对太湖沉积物无机氮和磷释放的影响,通过对比分析沉积物和上覆水无机氮浓度、沉积物和上覆水之间无机氮的循环规律及沉积物中无机氮的剖面特征在有/无水蚯蚓活动背景下的差异,探讨了寡毛类底...     

改性凹凸棒土及粉末活性炭助凝聚硅硫酸铝消除微污染水中有机氯

以硅酸钠和硫酸铝为原料制备了聚硅硫酸铝絮凝剂(PASS),采用强化混凝的处理方法,对微污染水中有机氯(OCPs)的消除进行了研究.同时,考察了混凝剂投加量、pH值、原水浊度、粉末活性炭和改性凹凸棒土助凝剂等因素对OCPs消除效果的影响.结果表明:PASS投加量为5 mg·L-1时,OCPs的去除率可以达到57%~87%,浊度去除率可以达到99.1%,其效果好于聚合氯化铝(PAC);PASS混凝处理OCPs的最佳pH值范围是6~7;OCPs的去除与浊度的去除具有显著相关性,原水浊度的大小会影响OCPs的去除,低浊条件下OCPs和浊度的去除率明显低于中浊和高浊条件;粉末活性炭和改性凹凸棒土作为助凝剂与PASS复配均可显著提高OCPs的去除率,分别达到78%~100%和72%~95%.相较而言,凹凸棒土储量丰富,廉价易得,因此,以改性凹凸棒土替代粉末活性炭更有优势.     

聚铁和氯化钙联用在污泥脱水中的实验研究

城市生活污水处理所产生的污泥含水率高,污泥脱水对处置场地、处理成本等方面有着重要影响,本文考察了不同药剂的污泥脱水效果。确定了聚合三氯化铁和氯化钙联用为最佳处理方法,不仅药剂投加量较小,且能有效去除污泥气味。最佳投加量为聚合三氯化铁:40.3kg/t,氯化钙:28kg/t,处理后污泥含水率为43.3%,实际污泥减量达到50%。     

氮在富营养化湖泊沉积物-水界面的释放

湖泊沉积物-水界面中的氮在特定条件下通过形态变化、界面特性和释放等途径影响湖泊水体质量。文章阐述了氮在湖泊沉积物-水界面的释放特征,并对影响氮在沉积物-水界面释放的因素进行了简要概述,并提出了几点控制水体释氮的建议。     

聚合氯化铁-腐殖酸(PFC-HA)冷冻干燥絮体的表面微观形貌及其孔表面分形特征

采用低温急速冷冻-真空干燥技术制备了不同pH(9.0、7.0、5.0)原水在45.89mg·L-1(以Fe3 计,原水pH=9.0)或28.41mg·L-1(以Fe3 计,原水pH=7.0、5.0)投药量下混凝后形成的PFC-HA絮体的粉末样品,研究了它们的表面微观形貌和孔表面分形特征.SEM图像表明,PFC-HA絮体具有不规则的块、片状形貌,而且在原水pH=9.0或pH=7.0时形成絮体也存在簇状结构.3种样品对N2的吸附-脱附等温线上均存在滞后圈,但样品3的形状不同.它们的吸附量、BJH累积吸附孔体积与脱附平均孔径的大小顺序均为:样品3＞样品2＞样品1,即随原水pH的降低而升高,而且孔尺度分布曲线显示样品3的表面存在大孔.BET比表面积的变化趋势与它们不一致,且样品2的比样品3稍大,样品1的最小.基于分形FHH方程,采用吸附等温线和脱附等温线数据计算出样品1和样品2的孔表面分形维Ds数均在2.94左右,而样品3的均小于2.38.这些Ds值似乎不能完全表示出因孔表面粗糙性而导致的空间填充能力的大小,主要表达了3种样品的中孔甚至大孔的尺度分布引起的不规则性.本试验中采用热力学模型计算出的3个样品Ds值大都超过3,它们已经失去了维数的实际意义;但样品3因其吸附-脱附等温线上的滞后圈接近圆桶式的A类,如果缩小分形标度区间,可以得到与分形FHH方程计算出的Ds接近的值.     

采用双氰胺甲醛缩聚物混凝去除水中酸性红B染料的研究

以双氰胺和甲醛为原料制备了聚合双氰胺甲醛,并对其进行红外光谱表征。采用聚合双氰胺甲醛与硫代硫酸钠共同作用对酸性红B染料溶液进行混凝脱色实验。对比了单独使用聚合双氰胺甲醛,以及聚合双氰胺甲醛与硫代硫酸钠共同作用的脱色效果。探讨了硫代硫酸钠和聚合双氰胺甲醛的用量以及pH值对脱色率的影响。结果表明,投加硫代硫酸钠可以明显地提高聚合双氰胺甲醛的脱色率,增大絮凝范围,使絮凝剂对pH值的变化有很强的适应性,pH值为7～12的范围内,脱色率均能维持在96％以上。此外,还对混凝脱色的机理进行了研究。