锆(Ⅳ)负载交联壳聚糖吸附硫酸根的性能

以甲醛、苯甲醛为交联剂,制备交联壳聚糖树脂,再与锆(Ⅳ)离子反应制备锆负载交联壳聚糖吸附剂。采用静态吸附法考察了该吸附剂对水中硫酸根离子(SO24-)的吸附性能。实验发现,吸附时间2 h,SO24-溶液初始浓度500 mg/L,pH值3.0,溶液温度35℃为较优的吸附条件;吸附过程符合Langmuir等温吸附模型,属于优惠吸附型,吸附容量可达78.65 mg/g;吸附过程较好地符合拟二级动力学模型;锆负载前后交联壳聚糖对硫酸根的吸附量提高了约4.5倍;该吸附剂具有良好的耐酸性和再生性能。     

丝胶蛋白的固定化及其对Cd~(2+)的吸附效果研究

通过固定化载体和制备方法的选择,以对Cd~(2+)的吸附量为考察指标,得到了固定化丝胶蛋白的最佳制备条件。结果表明,以壳聚糖为载体,采用包埋—交联法,在壳聚糖质量浓度为20g/L、煮茧废水与壳聚糖溶液体积比为1∶1、戊二醛体积分数为2%的条件下,制备的壳聚糖固定化丝胶蛋白成球效果好、易操作、机械强度适中,对Cd~(2+)的吸附量最大达到102.72mg/g。     

交联壳聚糖对重金属离子的吸附性能研究

以海蟹壳为原料制备的壳聚糖在碱性条件下,经环氧氯丙烷交联制得水不溶性的交联壳聚糖,采用静态法研究交联壳聚糖对Ｃｕ＾２＋,Ｃｒ＾３＋,Ｎｉ＾２＋,Ｐｂ＾２＋,Ｚｎ＾２＋,Ｈｇ＾２＋等几种重金属离子的吸附性能及ｐＨ值对吸附性能的影响,探讨了它们的作用机理。     

质子化改性交联壳聚糖的制备及其吸附硫酸根离子的性能

以壳聚糖为原料,甲醛为氨基保护剂,戊二醛为交联剂,采用反相悬浮交联法制备交联壳聚糖,再对其进行质子化改性得到质子化改性交联壳聚糖吸附剂。通过正交实验对该吸附剂的制备条件进行优化,并对其吸附水中硫酸根（SO₄^2-）的吸附等温特性和动力学进行研究,最后对制备和吸附过程进行能谱分析（EDS）并对吸附剂进行了再生实验。实验结果表明,交联反应的优化条件为：反应温度50℃、反应时间6 h、甲醛：戊二醛：壳聚糖为4.5：0.5：3（质量比）;该吸附过程符合Langmuir吸附等温模型,在25℃（298 K）下,吸附容量最大可达133.87 mg/g;吸附过程较好地符合拟二级动力学模型;EDS分析表明了交联反应、质子化改性和吸附反应均已发生;该吸附剂的再生性能良好,可以重复使用。     

交联壳聚糖珠吸附活性染料的动力学研究

利用交联剂环氧氯丙烷(ECH)对壳聚糖进行改性,制备了交联壳聚糖珠,对活性染料(活性艳蓝ST-RV)的脱色性能进行了研究。分别从起始染料浓度(100～200 g/cm3)、温度(30～50℃)以及pH(7～9)考察了对染料吸附的动力学影响。当起始染料浓度为200 g/cm3,温度30℃,pH=7时,交联壳聚糖珠对ST-RV的吸附量达到77.49 mg/g。用准一级和二级动力学模型描述了动力学数据并确定了速率常数,最后进行了交联壳聚糖珠的再生实验。结果表明,吸附数据符合二级动力学模型;当pH=10时,交联壳聚糖珠可少量解吸。     

交联菌丝体吸附剂的制备及其对Cr^3＋的吸附特性

深入研究了交联菌丝体吸附剂的制备工艺及其对Cr^3＋的吸附特性。交联菌丝体吸附剂制备工艺简单，但在制备过程中，活化剂NaOH和交联剂的用量对吸附特性影响较大。与纯菌丝体吸附剂相比，交联菌丝体吸附剂表观吸附容量提高48％，达到49．83mg／g（pH=2．53，水溶液中的Cr^3＋浓度为600mg／L），同时其机械强度明显增强。交联菌丝体吸附剂对Cr^3＋的吸附特点是将沉淀法与吸附法相结合，将沉淀与吸附两过程合二为一，从而简化了处理工艺，降低了处理成本。     

以硅胶为基质的交联壳聚糖对Ni2+的吸附研究

以硅胶为基质的交联壳聚糖作为重金属Ni^2 的吸附剂，对影响该吸附Ni^2 的因素及吸附剂的再生和其吸附能力的变化，吸附机理等进行了研究。结果显示，吸附剂在一定的实验条件下对Ni^2 的最高吸附量按每克壳聚糖计可达650mg/g，且吸附平衡时间短。在柱法实验中其吸附率在99．9％以上。     

交联菌丝体吸附剂的制备及其对Cr3+的吸附特性

深入研究了交联菌丝体吸附剂的制备工艺及其对Cr3+的吸附特性.交联菌丝体吸附剂制备工艺简单,但在制备过程中,活化剂NaOH和交联剂的用量对吸附特性影响较大.与纯菌丝体吸附剂相比,交联菌丝体吸附剂表观吸附容量提高48%,达到49.83 mg/g(pH=2.53,水溶液中的Cr3+浓度为600mg/L),同时其机械强度明显增强.交联菌丝体吸附剂对Cr3+的吸附特点是将沉淀法与吸附法相结合,将沉淀与吸附两过程合二为一,从而简化了处理工艺,降低了处理成本.     

MnO_2/Al_2O_3吸附草甘膦及微波紫外耦合降解再生工艺

以掺混煅烧法制备Mn O2/Al2O3,并对草甘膦进行吸附,将吸附态草甘膦置于微波紫外耦合系统中进行降解和再生。研究并给出了Mn O2/Al2O3的最佳制备条件、最佳吸附条件和微波紫外耦合降解再生的最佳工艺参数。Mn O2/Al2O3最佳制备条件为Mn O2质量分数15%,煅烧温度500℃,煅烧时间2 h。在常温下,Mn O2/Al2O3对草甘膦的最大吸附量为75 mg/g。微波紫外耦合系统最佳工艺参数为功率500 W,时间25 min,空气量0.06 m3/h。在此操作条件下,Mn O2/Al2O3的再生率达到85%,并且可以多次再生利用,草甘膦最终降解产物为二氧化碳、氮氧化物、磷酸和水,矿化率为65%。     

空心壳聚糖微球对二甲酚橙的吸附性能研究

以生物可降解的壳聚糖为原料,采用反相悬浮交联法制备了具有空壳结构的壳聚糖微球,通过控制反应条件得到单分散性的微米级微球.通过分光光度法探讨了溶液初始pH、吸附时间、二甲酚橙初始浓度、壳聚糖微球用量及其直径对壳聚糖微球吸附二甲酚橙的影响.结果表明,常温下壳聚糖微球对二甲酚橙的最佳吸附条件为:溶液初始pH为5,吸附时间为2.0 h,二甲酚橙初始质量浓度为32 mg/L,壳聚糖微球用量为0.3 g/L(以每升二甲酚橙溶液计),壳聚糖微球直径为74 靘;在此最佳吸附条件下,采用分光光度法对二甲酚橙模拟废水进行测定,相应的回收率误差均在-1%～1%.     

壳聚糖联合碱改性粉煤灰对重金属离子的吸附特性

采用浸渍法将壳聚糖负载在经NaOH改性的粉煤灰上,制备了联合改性的粉煤灰。随粉煤灰上壳聚糖负载量的增加,粉煤灰对Pb²⁺和Cd²⁺的吸附率均提高。当负载壳聚糖的质量分数为8%,吸附温度为30℃,吸附时间为120 min时,粉煤灰对Pb²⁺的吸附率最高（为98.9%）,对Cd²⁺的吸附率也最高（为91.5%）。其吸附行为符合Freundlich等温吸附模型,但表现为2个线性区。粉煤灰负载壳聚糖的改性机理是粉煤灰与带正电荷的壳聚糖的化学键合作用。     

Adsorption behavior of reactive dye in aqueous solution on chemical cross-linked chitosan beads

A batch system was applied to study the adsorption of reactive dye (reactive red 189) from aqueous solutions by cross-linked chitosan beads. The ionic cross-linking reagent sodium tripolyphosphate was used to obtain more rigid chitosan beads. To stabilize chitosan in acid solutions, chemical cross-linking reagent epichlorohydrin (ECH), glutaraldehyde and ethylene glycol diglycidyl ether was used and ECH shows a higher adsorption capacity. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms at different particle sizes and isotherm constants were determined. The Langmuir model agrees very well with experimental data and its calculated maximum monolayer adsorption capacity has very large value of 1802-1840 (g/kg) at pH 3.0, 30 degrees C. The kinetics of the adsorption with respect to the initial dye concentration, temperature, pH, ionic strength, and wet/dry beads were investigated. The pseudo-first-order, second-order kinetic models and intraparticle diffusion model were used to describe the kinetic data and the rate constants were evaluated. The dynamical data fit well with the second-order kinetic model, except for the dry beads fitting better with the first-order model. The adsorption capacity increases largely with decreasing solution pH or with increasing initial dye concentration. Thermodynamic parameters such as change in free energy (deltaG(0)), enthalpy (deltaH(0)), entropy (deltaS(0)) and activation energy were also determined. The adsorption mechanism is shown to be the electrostatic interactions between the dye and chitosan beads. The desorption data shows that the removal percent of dye RR 189 from the cross-linked chitosan beads is 63% in NaOH solutions at pH 10.0, 30 degrees C. The desorbed chitosan beads can be reused to adsorb the dye and to reach the same capacity as that before desorption.     

锰矿尾渣改性壳聚糖对Pb^2＋的吸附

将工业废弃物锰矿尾渣与壳聚糖混合制得一种高效吸附斛，并应用扫描电镜、X射线衍射对其结构进行了表征。采用正交表设计试验，分别考察了pH值、吸附时间、温度、复合吸附剂的投加量等4个影响因素对Pb^2＋吸附的影响，最佳吸附条件为：pH值为7，吸附时问为40mjn，温度为20℃，复合吸附剂的投加量为0．10g。处理后的水符合国家污水综合排放标准（GB8978．1996）中的一级标准。复合吸附剂对Pb^2＋的吸附符合Langmuir和Freundlich吸附等温方程。     

Preparation of alginate-chitosan hybrid gel beads and adsorption of divalent metal ions

Naturally occurring polysaccharides such as alginic acid and chitosan have been recognized as one of the most effective adsorbents to eliminating low levels of heavy metal ions from waste water stream. The present study intended to use alginic acid and chitosan simultaneously, which are expected to form a rigid matrix structure of beads due to electrostatic interaction between carboxyl groups on alginic acid and amino groups on chitosan, and to prepare alginate-chitosan hybrid gel beads. This could be achieved for the first time by using water-soluble chitosan, which was obtained by deacetylating chitin to 36-39% degree. The water-soluble chitosan dissolved in water could remain in solution in the presence of sodium alginate, and the homogeneous solution of chitosan and alginate was dispensed into a CuCl2 solution to give gel bead particles. The resultant beads were then reinforced by a cross-linking reaction of aldehyde groups on glutaraldehyde with amine groups on the chitosan. The cross-linking reaction made the beads durable under acidic conditions. The adsorption of Cu(II), Co(II), and Cd(II) on the beads was significantly rapid and reached at equilibrium within 10 min at 25 degrees C. Adsorption isotherms of the metal ions on the beads exhibited Freundlich and/or Langmuir behavior, contrary to gel beads either of alginate or chitosan showing a step-wise shape of adsorption isotherm.     

壳聚糖-沸石杂化膜的制备及其对甲基橙的吸附

采用物理共混法制备了壳聚糖-沸石杂化膜,用扫描电镜(SEM)和热重分析仪(TGA)对其进行表征,并系统地研究了壳聚糖-沸石杂化膜对甲基橙的吸附行为。结果表明,最佳质量配比为(沸石/壳聚糖)为1∶20;pH值对吸附的影响最为关键,在实验浓度的范围内对甲基橙溶液最大吸附量为974.05 mg/g。杂化膜对甲基橙的等温吸附行为符合Lang-muir模型,吸附动力学模式符合准二级动力学方程,考虑以化学吸附行为为主。杂化膜有良好的再生能力。     

盐酸和硝酸介质中己二胺接枝壳聚糖微球吸附Hg(Ⅱ)的行为

制备并表征了氯化和氨化壳聚糖微球,考察了己二胺接枝壳聚糖微球(HDA-CS)在盐酸和硝酸介质中吸附Hg(Ⅱ)的行为及影响因素。结果表明,盐酸介质中,pH 3.0时,HDA-CS对Hg(Ⅱ)有较高的初始吸附速率,最大吸附容量为128.6 mg/g;硝酸介质中,pH 3.5时,它对Hg(Ⅱ)的最大吸附容量为37.7 mg/g。前者是后者的3.4倍。以1.0 mol/L的H2SO4为解吸剂,HDA-CS复用3次无溶解和流失现象。HDA-CS对Hg(Ⅱ)的吸附主要是质子化氨基与汞配阴离子以静电引力实现的。     

Competitive adsorption of dye metanil yellow and RB15 in acid solutions on chemically cross-linked chitosan beads

One kind of adsorbent with a high adsorption capacity for anionic dyes was prepared using ionically and chemically cross-linked chitosan beads. A batch system was applied to study the adsorption behavior of one acid dye (MY, metanil yellow) and one reactive dye (RB15, reactive blue 15) in aqueous solutions by the cross-linked chitosan beads. The adsorption capacities was 3.56 mmol g(-1) (1334 mg g(-1)) for dye MY and 0.56 mmol g(-1) (722 mg g(-1)) for dye RB15 at pH4, 30 degrees C. The Langmuir model agreed very well with the experimental data (R(2)>0.996). The kinetics of adsorption for a single dye and the kinetics of removal of ADMI color value in mixture solutions at different initial dye concentrations were evaluated by the nonlinear first-order and second-order models. The first-order kinetic model fits well with the dynamical adsorption behavior of a single dye for lower initial dye concentrations, while the second-order kinetic model fits well for higher initial dye concentrations. The competitive adsorption favored the dye RB15 in the mixture solution (initial conc. (mM): MY=1.34; RB15=1.36); while it favored the dye MY in the mixture solution (initial conc. (mM): MY=3.00; RB15=1.34) and the adsorption kinetics for dye RB15 has the tendency to shift to a slower first order model.     

丙烯酸改性壳聚糖磁性颗粒处理模拟废水中氨氮

以去除水产养殖废水中的氨氮,寻找安全快速高效的吸附剂为目的。以壳聚糖为原料制备丙烯酸改性壳聚糖磁性颗粒,采用单因素及正交实验方法优化制备条件,研究振荡吸附条件对吸附量的影响,进行吸附等温模型和吸附动力学研究。结果表明,最佳制备条件,丙烯酸4 mL、磁流体0.75 g、过硫酸铵1 g、戊二醛1.5 mL;最佳吸附条件,废水pH值5~9、吸附剂浓度3 g/L、吸附时间10 min;吸附过程符合二级动力学模型,以化学吸附为主;液膜扩散为限速步骤;氨氮最大吸附量为77.16 mg/g,远高于其他传统吸附剂。研究表明,丙烯酸改性壳聚糖磁性颗粒对模拟水产养殖废水的氨氮去除效果显著,具有很好的应用前景。     

二氧化钛/碳纳米管/壳聚糖薄膜的制备及对苯的降解性能

研究了光催化降解挥发性有机化合物过程中催化剂二氧化钛/碳纳米管/壳聚糖薄膜的制备以及该催化剂对苯的光催化性能。首先采用溶胶-凝胶法制备纳米复合材料二氧化钛/碳纳米管,然后利用壳聚糖作为交联剂,制得二氧化钛/碳纳米管/壳聚糖复合材料催化薄膜。通过傅立叶红外光谱(FT-IR)、X射线衍射(XRD)透射电镜扫描(TEM)和紫外-可见光漫反射(UV-Vis)等技术分析了复合材料薄膜的组成、结构、形貌和对光的吸收性能,然后使用该催化剂对室内常见的污染物苯进行降解,并在同样的实验条件下,使用催化剂二氧化钛(P25)/壳聚糖对苯进行降解,对两者催化性能进行对比,结果表明,二氧化钛/碳纳米管/壳聚糖对苯有更强的吸附能力和更高的催化活性。