氨基酸在固／水界面的吸附作用

本文研究了活性炭、硅胶和氧化铝自水中吸附酪氨酸和苯丙氨酸。所得的结构表明,（1）在活性炭/水界面上两种氨基酸的吸附等温线均为Langmuir型。极限吸附量nm^S、吸附常数b与介质pH值关系曲线大约在氨基酸等电点处有最大值,这可用介质pH对氨基酸溶解度的影响解释。在活性炭表面,氨基酸主要以两性离子躺方式吸附。（2）在硅胶（氧化铝）/水界面上的吸附等温线为S型,吸附量仅为在活性炭/水界面上的1‰,在硅胶表面苯丙氨酸主要以电性作用吸附;在氧化铝表面酪氨酸以两性离子与表面形成氨键吸附。     

粉煤灰合成Na-X沸石去除废水中镍离子的研究

粉煤灰通过碱熔融 水热法合成了Na-X型沸石,研究了Na-X型沸石的用量、吸附时间、溶液pH值、初始镍离子浓度和温度对废水中镍离子去除效果的影响。结果表明,Na-X型粉煤灰沸石对镍离子的去除性能与化学原料合成的13X相当,明显优于粉煤灰。在20℃,pH值为6,沸石用量10g/L,吸附15min时,对初始浓度为20mg/L~150mg/L的镍离子去除率均可达90%以上。镍离子的吸附过程符合Langmiur吸附等温方程式,其单层吸附量为11.2×10^-3。粉煤灰沸石重复使用5次,对废水中镍离子的去除率仍高达95%,再生性能良好。     

黑膜厚度与膜表面张力关系的研究

用微干涉测量技术直接测定楔压等温线,研究了电解质浓度对阳离子表面活性剂TTAB在浓度大于cmc时形成黑膜厚度的影响及膜表面张力与溶液表面张力之间的差别.结果显示,黑膜厚度取决于楔压和电解质浓度,随着楔压的增加,液膜厚度减少至一定程度后几乎保持不变,表明黑膜类型的转化是阶跃式的,而电解质屏蔽了液膜两个表面电荷层间的排斥作用,故电解质浓度增加,液膜厚度变小.由楔压等温线得出的膜表面张力的结果说明一般黑膜的表面张力与溶液的表面张力并无明显差别.     

ZnO/C纳米球的亚甲基蓝单吸附特性:平衡、动力学及机理

采用电弧放电法制备了ZnO/C纳米球,利用FESEM、XRD和N₂吸附/脱附测试进行了表征。在避光条件下研究了复合材料对亚甲基蓝的吸附性能。研究结果表明,随着亚甲基蓝的浓度及接触时间的增长吸附量明显上升,在吸附时间为150 min时达到吸附平衡。采用Langmuir、Freundlich及Temkin等温吸附模式对吸附平衡进行了研究。结果表明,吸附等温线符合Langmuir等温吸附模式,单层吸附饱和容量可达188.68 mg·g^-1。利用动力学模型、内扩散模型和外扩散速率控制模型拟合实验数据,拟合数据表明其动力学符合伪二级动力学模型;内扩散机理不是吸附速率的唯一限制机理,亚甲基蓝的总吸附速率受膜扩散控制。     

A new fast swelling poly[DAPB-co-DMAAm-co-AASS] superabsorbent hydrogel for removal of anionic dyes from water

The objective of this research is to utilize a new poly[N,N-diallyl pyrrolidinium bromide-co-N,Ndimethyl acrylamide-co-acrylic acid sodium salt]superabsorbent hydrogel（SAH）for the removal of two anionic dyes,e.g.,Reactive Red 5B（RR5B）and Reactive Orange M2R（ROM2R）,from water.The SAH was characterized by swelling in water,FTIR,TGA and SEM.The SAH DDA6showed good swelling property and thermal stability.We have also investigated the parameters affecting dye adsorption such as pH,adsorbent dose,adsorption rate and initial dye concentration.The experimental data were also analyzed by applying the well known Langmuir and Freundlich isotherm models.     

纳米TiO-2对模型病毒-f2噬菌体的吸附特性

为了提高饮用水处理系统对病毒的去除效果,本研究采用静态实验,研究纳米TiO2对模型病毒—f2噬菌体的吸附去除特性,系统考察TiO2投加浓度、病毒浓度、温度及pH值等因素对吸附效果的影响.实验结果表明：f2噬菌体在纳米TiO2表面的吸附符合准二级吸附动力学模型,遵循化学吸附机理,颗粒内扩散为该吸附过程中的速率控制步骤,但不是唯一控制步骤;纳米TiO2对f2噬菌体的吸附符合Freundlich等温吸附模型（qe=27.4Ce1.24）,属于多层吸附类型;在20~40℃范围内,温度对纳米TiO2的吸附性能影响不大,而酸性条件下更有利于纳米TiO2对f2噬菌体的吸附.     

核桃壳对废水中Zn~(2+)的吸附研究

采用核桃壳吸附模拟废水中Zn2+,实验结果表明,25℃时,采用粒径为2.5~3.0mm的吸附剂0.6g,pH值为6.0,处理50mL浓度为5mg/L的含Zn2+模拟废水,吸附时间120min,Zn2+的去除率达62%。核桃壳对Zn2+的吸附行为符合拟二级动力学方程和Freundlich等温吸附方程,Zn2+浓度分别为2mg/L、5mg/L、10mg/L时,吸附速率分别为0.0624g/mg·min、0.0060g/mg·min、0.0055g/mg·min,最大吸附量为0.465mg/g。吸附剂再生使用5次后去除率下降,吸附剂内部孔隙率下降。     

Synthesis of new superabsorbent poly(NIPAAm/AA/N-allylisatin)nanohydrogel for effective removal of As(Ⅴ) and Cd(Ⅱ) toxic metal ions

The present studies highlight the effective removal of As（V） and Cd（II） from aqueous solutions by superabsorbent poly （NIPAAm/AA/N-allylisatin） nanohydrogel. Batch removal studies were performed as a function of treatment time, initial metal ion concentration, pH, and adsorbent dose. TEM micrographs confirm the particle size distribution in the range between 5 nm and 10 rim. The simple and metal ions adsorbed nanohydrogels were characterized by FF-IR, TGA, and EDX analysis. Finally, the equilibrium removal efficiency of the nanohydrogel was analyzed according to the Langmuir and Freundlich adsorption isotherm models which showed the removal of As（V） and Cd（II） metal ions fitted to Freundlich and Langmuir isotherms, respectively. Removal efficiency order of the metal ions is As（V） 〉 Cd（II）.     

Preparation of a novel chelating resin for the removal of Ni2+ from water

A new chelating resin DVB-MA-HDA modified with hydroxamic acid groups was prepared for the fast removal of Ni2＋ from water. SEM, BET, elemental analysis, FT-IR spectroscopy and XPS were used to characterize this new adsorbent. Batch adsorption experiment indicated that the equilibrium adsorption capacity of DVB-MA-HD for Ni2＋ was more than 130mg/g, and the adsorption isotherm can be well fitted by the Langmuir model. The adsorption kinetic curve indicates that more than 60% of the adsorption amount of Ni2＋ at equilibrium occurred within the initial 20 rain. 0.1 mol/L EDTA solution could desorb Ni2＋ from DVB-MA-HDA effectively.     

限域于SBA-15孔道内的活性相聚集形态

针对Pd/SBA-15和MoO3/SBA-15两类催化剂样品,使用N2物理吸附手段对比研究了限域于介孔SBA-15分子筛孔道内活性相Pd与MoO3的聚集形态.结果表明,金属Pd以颗粒状形态分布在SBA-15分子筛孔道内,氧化物MoO3则以层状形态存在.并用高分辨透射电镜验证了此分析结果.