表面活性剂对土壤粘粒絮凝-分散的影响

以浙江红壤为例,研究了两种阴离子表面活性剂和一种非离子表面活性剂对土壤粘粒悬浮液稳定性的影响.结果表明,表面活性剂对土壤粘粒的分散作用影响较大,且非离子表面活性剂的影响大于阴离子表面活性剂的影响.表面活性剂对土壤粘粒的分散作用主要是土壤颗粒对表面活性剂的电性吸附和配位吸附所致.表面活性剂进入土壤环境,会导致土壤粒子的分散,流动性增加;其结果是:一方面加重水土流失,另一方面使水环境污染程度加深.      

改性土壤对模拟含油废水中油的吸附

研究季铵盐阳离子表面活性剂四甲基铵离子 ( TMA)和十六烷基三甲基铵离子 ( HDTMA)改性的土壤 (黑土、黄棕壤、红壤 )对水中油的吸附作用 .结果表明 :改性土壤和未改性土壤均可吸附水中的油 ,但改性土壤对水中油的吸附能力明显高于未改性土壤 .改性土壤吸附油能力的顺序依次为 :1 CEC- HDTMA黑土 >1 CEC-HDTMA黄棕壤 >1 CEC- HDTMA红壤 >1 CEC-TMA黑土 >1 CEC-TMA黄棕壤 >1 CEC- TMA红壤 .未改性土壤和 HDTMA改性土壤对油的吸附通过分配来进行 ,吸附等温线可由 Henry方程表示 ,得出 logK_SOM为 2.69,logK_HDTMA为 3.35;TMA改性土壤对油的吸附符合 Langmuir方程 ,其对油的饱和吸附量分别为 1150 mg/kg( TMA黑土 ) ,751 mg/kg( TMA黄棕壤 ) ,172 mg/kg( TMA红壤 )     

电催化氧化法处理阴离子表面活性剂废水

采用自制电化学反应器对阴离了表面活性剂废水的电催化氧化处理进行了研究,考察了阳极材料、电解电压、电解时间、电极间距离、废水pH、废水电导率等对阴离子表面活性剂电解去除效果的影响,确定了最佳的处理条件。在电解电压为8V、电解时间为30～40min、电极间距离为2cm、废水pH为8～10、废水电导率为0．620ms／cm的条件下,阴离子表面活性剂的电解处理去除率可达96％以上。     

TMA改性粘土矿物对模拟地下水中苯系物的吸附

用短链季铵盐阳离子表面活性剂四甲基铵离子（ＴＭＡ）改性膨润土和凹凸棒土,研究它们对模拟地下水中苯系物的吸附作用。二种ＴＭＡ改性粘土矿物均可以有效地吸附模拟地下水中的苯系物,吸附机理较复杂,主要以表面吸附为主。     

UV/H2O2光催化氧化法处理表面活性剂废水

采用UV/H2O2光催化氧化法处理含表面活性剂废水,考察了反应时间、体系pH值、表面活性剂初始浓度、H2O2投加量、表面活性剂的种类等因素对处理效果的影响,并初步探讨了表面活性剂降解的反应动力学.结果表明,当初始pH值为4、H2O2投加量为1mL/L,反应时间为20min时,表面活性剂DBS的去除率为96%,AOS的去除率为93%,且UV/H2O2体系中,表面活性剂DBS和AOS的降解反应均符合表观拟一级反应动力学特征.     

腐殖酸钠和表面活性剂对黄土中石油污染物解吸增溶作用

选用十二烷基苯磺酸钠(LAS)、十二烷基硫酸钠(SDS)和十二烷基磺酸钠(SAS)对污染的土壤进行解吸实验,研究了这3种阴离子表面活性剂和腐殖酸钠对黄土中柴油类污染物的协同增溶作用.结果表明,腐殖酸钠和3种阴离子表面活性剂对黄土中柴油的解吸均有显著增溶作用,使柴油的解吸量明显增加,柴油的去除率最高可达63%.SDS对柴油的解吸量随腐殖酸钠浓度增大呈线性增加关系;但腐殖酸钠浓度增加对 LAS和SAS的解吸曲线有突越点,超过此浓度后反而会抑制解吸作用.     

Adsorption of mixed cationic-nonionic surfactant and its effect on bentonite structure

The adsorption of cationic-nonionic mixed surfactant onto bentonite and its effect on bentonite structure were investigated. The objective was to improve the understanding of surfactant behavior on clay mineral for its possible use in remediation technologies of soil and groundwater contaminated by toxic organic compounds. The cationic surfactant used was hexadecylpyridinium bromide (HDPB), and the nonionic surfactant was Triton X-100 (TX100). Adsorption of TX100 was enhanced significantly by the addition of HDPB, but this enhancement decreased with an increase in the fraction of the cationic surfactant. Part of HDPB was replaced by TX100 which decreased the adsorption of HDPB. However, the total adsorbed amount of the mixed surfactant was still increased substantially, indicating the synergistic effect between the cationic and nonionic surfactants. The surfactant-modified bentonite was characterized by Brunauer-Emmett-Teller specific surface area measurement, Fourier transform infrared spectroscopy, and thermogravimetric-derivative thermogravimetric/differential thermal analyses. Surfactant intercalation was found to decrease the bentonite specific surface area, pore volume, and surface roughness and irregularities, as calculated by nitrogen adsorption-desorption isotherms. The co-adsorption of the cationic and nonionic surfactants increased the ordering conformation of the adsorbed surfactants on bentonite, but decreased the thermal stability of the organobentonite system.     

不同表面活性剂改性有机膨润土的稳定性研究

文章利用CTMAB、DTMAB、CPB、DPB四种表面活性剂对膨润土进行了有机改性,并研究了改性后各有机膨润土在不同条件下的稳定性。实验结果表明,在同一影响因素下,CTMAB、CPB长碳链表面活性剂改性后的有机膨润土的稳定性较好,而DTMAB、DPB短碳链表面活性剂改性后的有机膨润土的稳定性较差。振荡时间、振荡强度,温度对有机膨润土的稳定性基本没有影响。超声波和pH处理可使有机膨润土的稳定性有所降低。随着处理溶液中NaCl、CaCl2浓度的提高,表面活性剂的烷基链含12个碳原子的改性有机膨润土的稳定性呈现先下降后逐渐上升的趋势。溶液中NaCl和CaCl2的浓度对烷基链含16个碳原子的表面活性剂改性的有机土的稳定性影响不大。     

Electrochemical study of sulfide solution in the presence of surfactants

Voltammetric curve studies on aqueous Na2S solution in the presence of three types of surfactants are presented. Presence of anodic surfactant (HTAB) in creases anode current density and makes the corresponding anode peak potential shift to more negative. Potentials of the reduction of elemental sulfur to intermediates Sx2-shift to more negative with the increasing of HTAB concentrations. In the presence of HTAB, the anode current density at 77oC increases more than at 34oC. The electrolysis indicates that anodic product sulfur loosely adhered to the graphite electrode surface when HTAB is added to the anolyte. The total efficiency of producing sulfur is high after several times of cycle electrolysis.The results show that anode passivation is minimized in the presence of HTAB. The depassivation effect of HTAB is discussed.     

表面活性剂溶液中多氯联苯溶解的特性

对表面活性剂溶液中多氯联苯的溶解特性进行了研究.发现非离子型表面活性剂对多氯联苯增溶效果优于阴离子型表面活性剂;在浓度大于临界胶束浓度(CMC)范畴,不但表面活性剂的增溶效果远较其浓度低于CMC时为佳,而且表面活性剂浓度与多氯联苯的溶解度成正比地线性相关,此结果说明,表面活性剂主要通过形成胶束来增加多氯联苯的溶解度.多氯联苯在非离子型表面活性剂胶束溶液中与在正己烷中的紫外-可见光谱相似,进一步说明胶束内的多氯联苯分子主要分布于类似正己烷的疏水胶核区域.在十二烷基醇聚氧乙烯(10)醚溶液中,所试多氯联苯的辛醇-水分配系数(K_ow)与其胶束-水分配系数(K_m)存在很好的线性相关关系.