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131.
以农作物秸秆为酶水解原料 ,用纤维素酶进行酶水解 ,水解液用于培养磷细菌肥生产菌 ,再用粉碎至一定粒度的作物秸秆对培养菌液进行吸附。实验结果表明 ,经酶解得到的水解液在添加一定的辅料后 ,可以作为培养磷细菌的料液。适宜条件下 ,菌量可达 5 1× 1 0 8/ml。 相似文献
132.
改性花生壳对苯酚的吸附 总被引:3,自引:0,他引:3
以花生壳为原料,使用环氧氯丙烷、二甲胺及吡啶,以N,N-二甲基甲酰胺为反应介质改性花生壳。结果表明:改性花生壳对苯酚的去除效果优于未改性花生壳。在实验条件下,吸附剂的吸附量在溶液pH为9,吸附时间为120 min时达到最大;溶液离子强度对吸附的影响较大。分析了该反应体系的动力学和热力学参数,改性花生壳吸附苯酚过程拟用准二级动力学模型处理,计算得出平衡吸附量与实验值相符。改性花生壳对苯酚的吸附符合Langmuir和Freundlich等温模式,R2均大于0.98,Qmax在84.49~108.76 mg/g之间,Freundlich模式的吸附强度n值在1.211~1.262之间,热力学参数△G、△H、△S表明改性花生壳对苯酚的吸附过程是自发、吸热过程。 相似文献
133.
Elisabetta Loffredo Marco Parlavecchia Giuseppe Perri Roberto Gattullo 《Journal of environmental science and health. Part. B》2013,48(8):728-735
AbstractIn this study, we used two biochars (BC) produced from grapevine pruning residues (BCgv) and red spruce wood (BCrs), two hydrochars (HC) from urban pruning residues (HCup) and the organic fraction of municipal solid wastes (HCuw), and two vermicomposts (VC) obtained vermicomposting digestates from buffalo manure (VCbm) and mixed feedstock (VCmf). Adsorption kinetics and isotherms of metribuzin onto these materials were performed. Sorption kinetics followed preferentially a pseudo-second-order model, thus indicating the occurrence of chemical interactions between the sorbate and the adsorbents. Adsorption constants were calculated using the Freundlich and Langmuir models. Metribuzin sorption data on BCgv and both HC fitted preferentially the Freundlich equation, whereas on the other materials data fitted both isotherms well (r?>?0.95). Metribuzin sorption capacity of the materials followed the trend BC?>?HC?>?VC. Sorption constants of metribuzin normalised per organic carbon content (KOC) on BCgv, BCrs, HCup, HCuw, VCbm and VCmf were 561, 383, 251, 214, 102 and 84?L kg?1, respectively. A significant positive correlation (P?=?0.016) was calculated between distribution coefficients (Kd) of all materials and the corresponding organic carbon contents, thus indicating a prominent role of the organic fraction of these materials in the adsorption of metribuzin. 相似文献
134.
以玉米淀粉为载体,采用液相还原法制备纳米零价铁/玉米淀粉,并用于溶液中Pb2+的去除。采用SEM技术对吸附材料进行了表征。考察了溶液pH、纳米零价铁/玉米淀粉加入量、初始Pb2+质量浓度、反应时间等因素对Pb2+吸附效果的影响。表征结果显示,纳米零价铁/玉米淀粉球体间主要呈链状连接,不仅保持了纳米零价铁的特性,且颗粒的团聚现象明显减少。实验结果表明,在溶液pH 7.0、纳米零价铁/玉米淀粉加入量0.8 g/L、初始Pb2+质量浓度50 mg/L、反应时间60 min的条件下,纳米零价铁/玉米淀粉对Pb2+具有较好的吸附效果,Pb2+去除率为93.17%、吸附量为47.27 mg/g。 相似文献
135.
136.
Adsorption enhancement of laterally interacting phenol/aniline mixtures onto nonpolar adsorbents 总被引:1,自引:0,他引:1
Adsorption equilibria of phenol and aniline onto nonpolar macroreticular adsorbents were investigated in single and binary-solute aqueous systems at 293 K and 313 K. All adsorption isotherms can be well represented by the Langmuir equation. Larger uptake of aniline than phenol onto all the adsorbents probably results from the higher hydrophobicity of the former compound as well as the greater electronic density of the aromatic ring of aniline. It is interestingly observed that at a relatively high loading, the total uptake of phenol and aniline in a binary system is remarkably higher than those in a single system. Such uptake difference was elucidated by the cooperative effect arising from the lateral acid–base interaction between the loaded phenol and aniline molecules. Moreover, larger average pore size of the adsorbent is found to result in a greater cooperative coefficient, as observed from the equimolar phenol/aniline adsorption system. 相似文献
137.
138.
A new approach to vapor phase elemental mercury capture has been explored; this approach exploits an ionic liquid coating
layer to oxidize elemental mercury for subsequent immobilization by chelating ligands. The room temperature ionic liquid 1-butyl-1-methyl
pyrrolidinium bis(trifluoromethane sulfonyl)imide (P14) was selected for study based on its oxidation potential window, thermal stability, and low vapor pressure. Tests were also
completed in which KMnO4 was added to P14 to form a new ionic liquid, P14–KMnO4, with a higher oxidation potential. In room-temperature bulk liquid phase capture experiments, 59% of the elemental mercury
in the inlet gas was captured using P14 alone; mercury capture using P14–KMnO4 was quantitative. P14 and P14–KMnO4 coatings were successfully applied to mesoporous silica substrates and to silica substrates functionalized with mercury chelating
ligands. The coating layers were found to be thermally stable up to 300°C. Fixed-bed tests of nonfunctionalized silica coated
with P14 showed an elemental mercury uptake of 2.7 mg/g adsorbent at 160°C; at the same temperature, functionalized silica coated
with P14–KMnO4 showed an elemental mercury capacity of at least 7.2 mg/g adsorbent, several times higher than that of activated carbon.
The empty bed gas residence time in these tests was 0.04 s. A chelating adsorbent incorporating P14 in the coating layer, may be capable of simultaneous removal of elemental and oxidized mercury from coal combustion flue
gases. 相似文献
139.
以2,6-二氨基吡啶为原料,合成了功能单体2-丙烯酰-6-氨基吡啶,并将其与乙二醇二甲基丙烯酸酯共聚合成了聚合物吸附剂聚丙烯酰-6-氨基吡啶。考察了聚合物吸附剂对重金属离子的吸附分离性能。实验结果表明:在混合液中Cu2+,Zn2+,Cd2+,Ni2+的初始质量浓度均为10 mg/L、聚合物吸附剂加入量为5 g/L、溶液pH=7、吸附时间为10 min的条件下,聚合物吸附剂对各离子的吸附率均大于90%;采用浓度为0.5 mol/L的HCl溶液对吸附后的聚合物吸附剂进行洗脱,4种重金属离子的洗脱率均可达97%以上;该吸附剂具有很好的稳定性,重复使用11次后其对4种重金属离子的饱和吸附量均未有明显的下降。 相似文献
140.
利用新型稀土铈铁复合吸附剂去除水体腐殖质的研究 总被引:4,自引:0,他引:4
研究了稀土铈铁复合材料(CFA)对水体中黄腐酸(FA)的去除效能和作用机制.结果表明:CFA在平衡pH3.0~6.5的范围内对FA的去除效果较好,吸附速度快,120min即达到平衡.水体中FA与砷酸根在CFA上有很强的竞争作用,当FA加入量为5mg/L~10mg/L时,砷的饱和吸附量Qo即丧失40%~50%,表明两者作用于材料相同的活性位点.吸附前后的红外谱图(FTIR)揭示了CFA表面羟基在FA去除中起着重要作用.通过Zeta电位的测定得出材料的等电点为5.6,因而pH偏酸性的条件有利于FA的去除. 相似文献