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1.
聚乙烯醇包埋龟裂链霉菌对水中Pb~(2 )吸附性能的研究   总被引:4,自引:0,他引:4  
本文研究了聚乙烯醇包埋龟裂链霉菌菌丝体的包埋条件及包埋后对水中Pb2 的吸附作用。结果表明,包埋比例为3/1(W/W),聚乙烯醇浓度为10%,海藻酸钠浓度0.2%,在含2?Cl2饱和硼酸溶液中固化24h是包埋反应的最佳条件。包埋后的饱和吸附量可达73.0mg/g,比未包埋龟裂链霉菌下降 47.1% 。pH值对吸附量的影响较包埋前下降。升高温度有利于吸附。  相似文献   

2.
本研究以菹草为原料,采用化学共沉淀方法制备Fe3 O4/菹草磁性纳米材料并应用于刚果红染料的吸附实验中.探究了pH、吸附时间、吸附剂用量、温度四个因素对吸附效果的影响.研究结果表明:该材料吸附刚果红的最佳条件为初始浓度为20 mg·L-1时,pH值为5,吸附剂投加量0.2 g,吸附时间4 h及温度为30℃;在最佳吸附条...  相似文献   

3.
考察了NKA-9、S-8、XDA-1、AB-8、HPD-100、HPD-600 6种大孔吸附树脂对宁夏枸杞总黄酮的吸附和解吸性能,筛选出XDA-1树脂的效果最佳;考察了pH值、样液浓度、流速等对XDA-1树脂静态吸附效果的影响;并进行了动态吸附试验,确定出XDA-1树脂动态吸附枸杞总黄酮的最佳条件:样品液浓度为0.25mg/mL,控制流速为0.5mL/min,样品液pH 5;最佳洗脱条件:洗脱液为80%的乙醇水溶液,用量为35mL (5倍柱床体积).在此条件下,枸杞总黄酮含量从27.2%提高到79.8%,回收率为87.4%,表明XDA-1树脂可用于宁夏枸杞总黄酮的分离纯化.  相似文献   

4.
研究了 pH对初加工甲壳素(A)和商品甲壳素(B)吸附性能的影响,通过加入电解质NaCl和表面活性剂十二烷基硫酸钠(SDS)探究了 pH影响甲壳素吸附性能的原因,并对吸附机理做了初步探讨.结果表明:甲壳素A和甲壳素B在pH 4.0时对碱性橙Ⅱ吸附效果最佳;加入0.1 mol/L NaCl后,在低pH条件下会对甲壳素与碱...  相似文献   

5.
明胶包埋黑根霉菌丝体对水中Pb^2+吸附性能的研究   总被引:12,自引:0,他引:12  
本文研究了明胶包埋黑根霉菌丝体的包埋条件及包埋后对水中Pb~(2+)的吸附作用。结果表明,包埋比例为6/1(W/W),交联剂甲醛用量为25%,凝胶化温度为40℃,PH=10.0为包埋反应的最佳条件。包埋后的饱和吸附量可达121.2mg/g,比未包埋黑根霉下降10.8%。吸附平衡时间延长至800分钟。pH值对吸附量有较大影响,PH=4.0时,吸附最佳。升高温度有利于吸附。流速对动态吸附有很大影响。HNO3和NaOH可以对吸附剂进行解吸与再生,解吸率在94%以上。明胶包埋后黑根霉具有较好的物理性能,断裂压缩强度为128.1N/cm2。  相似文献   

6.
壳聚糖经双氧水降解得到低分子量壳聚糖,用水杨醛对低分子量壳聚糖进行化学改性得到其相应的衍生物.分别研究了壳聚糖和水杨醛改性的低分子量壳聚糖对锆(Ⅳ)离子的吸附,考察了锆(Ⅳ)离子起始浓度、溶液pH值、吸附时间以及温度对这两种吸附剂吸附锆(Ⅳ)离子性能的影响,得出了最佳吸附条件.用红外对最佳条件下的吸附产物进行了表征.结果表明,壳聚糖吸附锆离子的最佳条件为:锆(Ⅳ)离子的起始浓度为6.5×10-4g/mL,振摇时间为6.5h,pH值为5~6;水杨醛改性的低分子量壳聚糖吸附锆离子的最佳条件为:锆离子的起始浓度为4.7×10-4g/mL,振摇时间为5h,pH值为5~6.这两种吸附剂对锆(Ⅳ)离子的吸附受温度影响均不大,吸附行为均满足Langmuir等温式.红外光谱分析表明,锆(Ⅳ)离子与这两种吸附剂均发生了配位作用.  相似文献   

7.
竹炭对砷(Ⅲ)离子的吸附行为研究   总被引:1,自引:0,他引:1  
研究了溶液的pH值与初始质量浓度、竹炭用量、吸附时间以及温度等因素对As(Ⅲ)离子吸附效果的影响。研究结果表明,在pH为3.00和12.50的情况下,竹炭对As(Ⅲ)离子有较好的吸附效果;同时吸附率随初始质量浓度的增加而降低,吸附能在180min内达到吸附平衡;等温吸附服从Freundlieh吸附等温方程式,酸性条件和碱性条件的最佳吸附温度分别为30℃和40℃。认为竹炭可作为理想的除砷吸附材料。  相似文献   

8.
腐植酸对砷的吸附作用研究   总被引:4,自引:0,他引:4  
腐植酸中含有大量的极性基团,对金属离子有较强的吸附性能。运用氢化物-原子荧光光谱法,以泥炭腐植酸为原料,研究了腐植酸对砷(V)离子的吸附作用和腐植酸吸附剂中砷的回收,并得出了最佳的吸附和脱附条件。实验考察了酸度、时间分别对吸附和脱附的影响。结果表明,泥炭腐植酸对砷吸附的最佳模型为Freundlich吸附方程,当溶液成中性时腐植酸对砷的吸附量较大且趋于平稳。砷的浓度为1μg/mL,溶液的pH值为7,吸附时间控制在55min时,吸附效果最佳,最大吸附率为85.49%。脱附的最佳条件为:pH值14,脱附时间20min。  相似文献   

9.
聚乙烯醇包埋龟裂链霉菌对水中Pb^2+吸附性能的研究   总被引:4,自引:0,他引:4  
本文研究了聚乙烯醇包埋龟链霉菌菌丝体的包埋条件及包埋后对水中Pb^2+的吸附作用。结果表明,包埋比例为3/1(W/W),聚乙烯醇浓度为10%,少藻酸钠浓度0.2%,在含2%CaCl2饱和硼酸溶液中固化24h是包埋反应的最佳条件,包埋后的饱和吸附量可达73.0mg/g,比未包埋龟裂链霉菌下降47.1%,PH值对吸附量的影响较包埋前下降。升高温度有利于吸附。  相似文献   

10.
魏燕芳 《广州化学》2010,35(4):29-34
用壳聚糖包埋磁流体,用戊二醛交联制成磁性壳聚糖微球,并用红外光谱表征其结构。用制备的磁性壳聚糖微球吸附Cr(Ⅵ)离子,考察了其对Cr(Ⅵ)离子的吸附性能;探讨了吸附时间、溶液pH值、吸附剂用量、温度、Cr(Ⅵ)起始浓度以及其他离子存在对Cr(Ⅵ)离子去除率的影响。实验结果表明,磁性壳聚糖微球吸附Cr(Ⅵ)离子的最佳条件为:吸附平衡时间40 min,最佳吸附pH值6左右,磁性壳聚糖微球用量10 mg,温度升高有利于提高磁性壳聚糖微球的吸附效率,Cr(Ⅵ)离子起始质量浓度为12μg/mL,无机盐的存在引起磁性壳聚糖微球的吸附性能降低。并且考察了吸附剂的再生性能,实验结果表明磁性壳聚糖微球具有良好的重复使用性。  相似文献   

11.
The adsorptive removal of lead (II) from aqueous medium was carried out by chemically modified silica monolith particles. Porous silica monolith particles were prepared by the sol-gel method and their surface modification was carried out using trimethoxy silyl propyl urea (TSPU) to prepare inorganic–organic hybrid adsorbent. The resultant adsorbent was evaluated for the removal of lead (Pb) from aqueous medium. The effect of pH, adsorbent dose, metal ion concentration and adsorption time was determined. It was found that the optimum conditions for adsorption of lead (Pb) were pH 5, adsorbent dose of 0.4 g/L, Pb(II) ions concentration of 500 mg/L and adsorption time of 1 h. The adsorbent chemically modified SM was characterized by scanning electron microscopy (SEM), BET/BJH and thermo gravimetric analysis (TGA). The percent adsorption of Pb(II) onto chemically modified silica monolith particles was 98%. An isotherm study showed that the adsorption data of Pb(II) onto chemically modified SM was fully fitted with the Freundlich and Langmuir isotherm models. It was found from kinetic study that the adsorption of Pb(II) followed a pseudo second-order model. Moreover, thermodynamic study suggests that the adsorption of Pb(II) is spontaneous and exothermic. The adsorption capacity of chemically modified SM for Pb(II) ions was 792 mg/g which is quite high as compared to the traditional adsorbents. The adsorbent chemically modified SM was regenerated, used again three times for the adsorption of Pb(II) ions and it was found that the adsorption capacity of the regenerated adsorbent was only dropped by 7%. Due to high adsorption capacity chemically modified silica monolith particles could be used as an effective adsorbent for the removal of heavy metals from wastewater.  相似文献   

12.
In this work, we report the first application of ion‐imprinted technology via precipitation polymerization for simple and practical determination of rubidium ions. The rubidium‐ion‐imprinted polymer nanoparticles were prepared using dibenzo‐21‐crown‐7 as a selective ligand, methacrylic acid as functional monomer, ethylene glycol dimethacrylate as cross linker, and 2,2′‐azobisisobutyronitrile as radical initiator. The resulting powder material was characterized using scanning electron microscopy, which showed colloidal nanoparticles of 100–200 nm in diameter and slightly irregular in shape. The maximum adsorption capacity of the ion imprinted particles was 63.36 μmol/g. The experimental conditions such as nature and concentration of eluent, pH, adsorption and desorption times, weight of the polymer material, aqueous phase and desorption agent volumes were also studied. Finally, selectivity of the prepared IIP particles toward rubidium ion was investigated in the presence of some foreign metal ions.  相似文献   

13.
纳米钛酸钙粉体的制备及其对水中铅和镉的吸附行为   总被引:2,自引:0,他引:2  
张东  侯平 《化学学报》2009,67(12):1336-1342
采用柠檬酸络合溶胶-凝胶法制备了纳米钛酸钙粉体. 以X射线衍射(XRD)、透射电子显微镜(TEM)和傅立叶变换红外光谱(FTIR)对其进行了表征. 考察了该纳米粉体对水中重金属铅和镉的吸附性能, 并以镉离子为例, 系统地研究了吸附热力学和动力学. 结果表明, 该法合成的钛酸钙为钙钛矿结构的纳米粉体, 粒径大小受灼烧温度的影响, 灼烧温度越高, 粉体平均粒径越大, 600 ℃灼烧2 h条件下, 粉体的平均粒径最小, 约为20 nm. 当介质的pH值为4~8时, 钛酸钙对水中的铅和镉具有很强的吸附能力. 其对镉离子的吸附行为符合Langmuir 吸附等温模型和HO准二级动力学方程式, 吸附过程焓变(ΔH)为39.312 kJ•mol-1, 各温度下的自由能变(ΔG)均小于零, 熵变(ΔS)均为正值, 吸附过程的活化能(Ea)为20.359 kJ•mol-1. 该吸附过程是自发的吸热物理过程. 被吸附的铅和镉均可用1 mol•L-1的硝酸完全洗脱回收. 对铅和镉的富集因子均超过200. 将其应用于水中痕量铅和镉的吸附富集和测定, 回收率分别为96.3%~107.2%和93.5%~104.0%, 与石墨炉原子吸收光谱法测定结果一致.  相似文献   

14.
离子交换树脂吸附镉的动力学研究   总被引:27,自引:3,他引:27  
实验采用离子交换法吸附氯盐体系中的镉,用动态法对2017型强碱性阴离子交换树脂的工作条件进行了优化,在最佳反应体系下,用批式离子交换法研究了温度、溶液浓度和树脂粒径对交换过程的影响,并用动边界模型描述交换过程的动力学,确定了离子交换行为的速度控制步骤为颗粒扩散,并推算出了交换过程的表观活化能、反应级数、速率常数和动力学总方程式。  相似文献   

15.
嗜铅菌对水中重金属Pb~(2+)的吸附研究   总被引:3,自引:0,他引:3  
研究了实验室提供的嗜铅菌对水中铅离子吸附的条件和机理.讨论了吸附时间、pH、铅离子的质量浓度和菌的质量浓度对吸附的影响.结果表明,在pH=7.0、铅离子初始质量浓度为25mg/L、离心湿菌的质量浓度为1.06g/L、吸附时间为60min时,铅离子的吸附率达96.88%;实验条件下超标25倍的含Pb~(2+)废水,可迭排放标准;Pb~(2+)的最大吸附量为150mg/g.数学模型Langmuir和Freundlich方程均能很好地描述嗜铅菌对Pb~(2+)的吸附过程.对Pb~(2+)吸附前后的红外光谱表征表明,嗜铅菌表面多糖、蛋白质的羟基峰和羰基峰均有不同程度的紫移,羟基峰、糖苷峰等峰宽略增,说明菌体吸附,主要是表面基团的作用所致.用原子力显微镜对吸附前后的嗜铅菌检测可见,吸附后菌体的弹性变小、粘性变大、部分茵体有一定的收缩,说明以表面吸附为主的吸附过程,对菌细胞的聚合度有影响,菌体内部对铅也有一定的生物积累.  相似文献   

16.
以Pb2+为模板,壳聚糖为单体,硅胶为载体,γ-(2,3环氧丙氧)丙基三甲氧基硅烷(KH-560)为偶联剂,利用表面分子印迹技术和溶胶-凝胶法制备了Pb2+ 印迹聚合物.采用傅立叶变换红外光谱法(FT-IR)、紫外光谱法、扫描电镜对Pb2+ 印迹和非印迹聚合物的表面形貌和结构进行表征;并用电感耦合等离子体原子发射光谱法考察了吸附酸度、吸附剂用量、静置时间等对聚合物吸附性能的影响;研究了印迹聚合物在混合溶液中对Pb2+ 的选择性,比较了印迹和非印迹聚合物的吸附容量;并提出了印迹聚合物的印迹吸附机理.在最佳吸附酸度pH=4.5时,0.3 g 吸附剂吸附5 h达到平衡,Pb2+印迹聚合物对模板离子具有较高的选择性,其饱和吸附容量是非印迹聚合物的2倍.  相似文献   

17.
Summary Metal ions are adsorbed in the interlayer space and on the edges of clay minerals, leading to the uniform distribution of metal ions on atomic scale. However, additional processes can be resulted in the formation of nano and micro particles in the interlayer space as well as on the outer surfaces. The formation of nano and micro particles on clay minerals under environmental conditions are discussed here in metal ions (manganese, lead, zinc, and silver ions)/bentonite systems. Two-dimensional nano layer is formed in the interlayer space by the oxidation of manganese ions under atmospheric conditions. Three-dimensional particles are formed on the surfaces initiating by the metal ion adsorption on the deprotonated edge sites. The formation of micro particles on the surface can also be followed by the redox reaction of metal ions.  相似文献   

18.
A study was conducted concerning the preparation and application of a novel synthetic oxide adsorbent of MgO-SiO2 type. The material was prepared via a sol–gel route, utilizing magnesium ethoxide and tetraethoxysilane as precursors of magnesium oxide and silica respectively, and ammonia as a catalyst. The powder was comprehensively analyzed with regard to chemical composition (EDS method), crystalline structure, morphology, characteristic functional groups, electrokinetic stability and porous structure parameters (BET and BJH models). The synthesized oxide adsorbent is amorphous, with irregularly shaped particles, a relatively large surface area of 612 m2/g, and negative surface charge over almost the whole pH range. Comprehensive adsorption studies were performed to investigate the adsorption of Cd(II) and Pb(II) ions on the MgO–SiO2 oxide adsorbent, including evaluation of adsorption kinetics and isotherms, the effect of pH, contact time and mass of adsorbent. It was shown that irrespective of the conditions of the adsorption process, the synthesized MgO–SiO2 adsorbent exhibits slightly better affinity to lead(II) than to cadmium(II) ions (sorption capacity of 102.02 mg(Pb2+)/g and 94.05 mg(Cd2+)/g). The optimal time for removal of the analyzed metal ions was 60 min, although adsorption reached equilibrium within 10 min for Pb(II) and within 15 min for Cd(II) ions, which was found to fit well with a type 1 pseudo-second-order kinetic model. Additionally, adsorption efficiency was affected by the pH of the reaction system—better results were obtained for pH ≥7 irrespective of the type of metal ion.  相似文献   

19.
板栗内皮对水溶液中镉离子和铅离子的吸附   总被引:1,自引:0,他引:1  
研究了板栗内皮对水溶液中金属离子(Cd2+,Pb2+)的吸附过程,以及吸附过程中不同条件对其吸附能力的影响.通过对反应时间、温度、pH、初始金属离子浓度等因素的控制,设计不同单一变量确定在不同条件下的吸附能力,利用红外光谱确定板栗内皮上参与反应的主要基团.结果表明,板栗内皮吸附Cd2+,Pb2+理论最佳吸附条件分别为p...  相似文献   

20.
A novel copper-based MOFs adsorbent(Cu-BTC-Th) was prepared using an one-step method by introducing a new organic ligand of 4-thioureidobenzoicacid(Th) with active groups for selectively adsorbing Pb(Ⅱ) from aqueous solutions. The chemical composition and structure of the prepared MOFs materials were characterized by scanning electron microscope(SEM), X-ray diffraction(XRD), fourier transform infrared spectroscopy(FTIR), X-ray photoelectron spectroscopy(XPS), Brunner-Emmet-Teller(BET) analysis, ...  相似文献   

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