活性炭纤维对水中微囊藻毒素的吸附性能

利用活性炭纤维对水中微囊藻毒素MC—LR的吸附,研究了吸附过程的热力学与动力学特性。结果表明,活性炭纤维对MC—LR的平衡吸附量在相同温度下随MC-LR初始浓度的增加而显著增大,并随着温度升高而增加,最大吸附量达246μg／g。不同温度条件下,活性炭纤维对MC-LR的吸附均较好地符合Langmuir等温吸附模型。通过热力学分析发现,△H=15．7kJ／mol、△G〈0、△S〉0,表明该吸附是自发的、吸热的过程,温度升高有利于吸附反应。动力学研究表明,该过程符合一级动力学方程。吸附反应速率受颗粒内扩散和液膜扩散共同影响。活性炭纤维经再生后,平衡吸附量变化较小,具有良好的重复使用性能。     

Cyanide Removal by Chinese Vegetation. Quantification of the Michaelis-Menten Kinetics (6 pp)

Background Little is known about metabolism rates of environmental chemicals by vegetation. A good model compound to study the variation of rates among plant species is cyanide. Vascular plants possess an enzyme system that detoxifies cyanide by converting it to the amino acid asparagine. Knowledge of the kinetic parameters, the half-saturation constant (Km) and the maximum metabolic capacity (vmax), is very useful for enzyme characterization and biochemical purposes. The goal of this study is to find the enzyme kinetics (KM and vmax) during cyanide metabolism in the presence of Chinese vegetation, to provide quantitative data for engineered phytoremediation, and to investigate the variation of metabolic rates of plants. Methods Detached leaves (1.0 g fresh weight) from 12 species out of 9 families were kept in glass vessels with 100 mL of aqueous solution spiked with potassium cyanide at 23°C for 28 h. Four different treatment concentrations of cyanide were used, ranging from 0.44 to 7.69 mg CN/L. The disappearance of cyanide from the aqueous solution was analyzed spectrophotometrically. Realistic values of the half-saturation constant (KM) and the maximum metabolic capacity (vmax) were estimated by a computer program using non-linear regression treatments. As a comparison, Lineweaver-Burk plots were also used to estimate the kinetic parameters. Results and Discussion The values obtained for KM and vmax varied with plant species. Using non-linear regression treatments, values of vmax and KM were found in a range between 6.68 and 21.91 mg CN/kg/h and 0.90 to 3.15 mg CN/L, respectively. The highest vmax was by Chinese elder (Sambucus chinensis), followed by upright hedge-parsley (Torilis japonica). The lowest vmax was demonstrated by the hybrid willow (Salix matssudana x alba). However, the highest KM was found in the water lily (Nymphea teragona), followed by the poplar (Populus deltoides Marsh). The lowest KM was demonstrated by corn (Zea mays L.). The values of vmax were normally distributed with a mean of 13 mg CN/kg/h. Conclusions Significant removal of cyanide from aqueous solution was observed in the presence of plant materials without phytotoxicity, even at high doses of cyanide. This gives rise to the conclusion that the Chinese plant species used in this study are all able to efficiently metabolize cyanide, although with different maximum metabolic capacities. A second conclusion is that the variation of metabolism rates between species is small. All these plants had a similar KM, indicating the same enzyme is active in all plants. Recommendations and Outlook Detoxification of cyanide with trees seems to be a feasible option for cleaning soils and water contaminated with cyanide. For phytoremediation projects, screening appropriate plant species adapted to local conditions should be seriously considered. More chemicals should be investigated to find common principles of the metabolism of environmental chemicals by plants.     

铬渣秸秆共热解产物铬稳定性研究

生物质铬渣共热解工艺是新型的铬渣处理工艺,该工艺能有效地将铬渣中的Cr(Ⅵ)还原为Cr(Ⅲ).而由于共热解产物总铬含量较高,因此考察了铬渣与秸秆共热解过程中铬稳定性.通过考察共热解产物成分及形态分析、pH影响实验、淋洗实验及长期稳定性实验,对共热解铬渣的铬环境安全性进行评估.结果表明:(1)共热解温度对铬渣形态有较大影响,可交换态及碳酸盐结合态铬含量随共热解温度升高而逐渐降低,800℃时候可交换态铬降至＜0.1％(质量分数,下同),碳酸盐结合态铬为1.2％;共热解后最稳定的残渣态铬含量随共热解温度升高而逐渐升高.(2)当pH＞7时,两种共热解产物总铬溶出量极低,基本都小于6mg/kg;当pH≤7时,总铬的溶出量显著增加,最高超过500 mg/kg.但由于解毒铬渣的酸中和能力极强,因此铬释放风险较低.(3)共热解产物的总铬累积溶出量极低,根据拟合结果计算出其100年填埋时间的总铬溶出量不超过1.3 mg/kg.长期稳定性实验表明,自然堆置过程中共热解产物的Cr(Ⅵ)含量逐渐降低.     

CS/PEG/PFT膜制备及对含铜废水的处理

实验将溶胶凝胶法和高分子辅助倒相法结合,制备出一种新型的壳聚糖/聚乙二醇/亚铁氰化钾钛(CS/PEG/PFT)复合膜,通过FT-IR和SEM对膜进行表征后,将其用于模拟铜废水的吸附和脱附实验,并探究出膜吸附的最佳工艺条件为:p H 5.50、实验温度55℃、实验时间2 h,该条件下,膜对铜离子最大吸附量为9.85 mg/g,去除率达到95%以上。CS/PEG/PFT膜的除铜过程符合Langmuir等温吸附方程(y=0.0597x+0.0168),线性相关度达到0.9917。     

Sorption of radiolabelled glyphosate on biochar aged in contrasting soils

Glyphosate mobility from terrestrial to aquatic environments has raised concerns about it. Utilizing soil’s inherent properties along with sorption properties of aged biochar, we hypothesized that selective application of biochar would be more effective in economic terms for glyphosate sorption on contrasting soils. To test this hypothesis, batch experiments and liquid scintillation counting for ¹⁴ Okada, E.; Costa, J. L.; Bedmar, F. Adsorption and mobility of glyphosate in different soils under no-till and conventional tillage. Geoderma 2016, 263, 78–85.[Crossref], [Web of Science ®] , [Google Scholar]C labeled glyphosate were used. The sorption behavior of glyphosate was examined in four contrasting Australian soil types (Oxisol, Vertisol, Entisol, and Inceptisol) amended with aged biochar to determine glyphosate concentrations by measuring ¹⁴ Okada, E.; Costa, J. L.; Bedmar, F. Adsorption and mobility of glyphosate in different soils under no-till and conventional tillage. Geoderma 2016, 263, 78–85.[Crossref], [Web of Science ®] , [Google Scholar]C activity using liquid scintillation counting. Freundlich parameters were calculated for soil-soil/biochar combinations. The pattern of glyphosate sorption was Oxisol?>?Vertisol?>?Entisol?>?Inceptisol. Oxisol adsorbed approximately five times more glyphosate compared with Inceptisol. Oxisol soil system adsorbed maximum amount of glyphosate principally due to the presence of iron-aluminum oxides exhibiting variable charges which got increased due to the presence of aged biochar. Considering all the soil/soil-biochar systems, Inceptisol soil system showed the least adsorption of glyphosate. A significant contribution of char was observed only in the Entisol soil system and the finding is valuable as char can be applied in Entisol soil systems to control glyphosate mobility.     

粉末活性炭对三烯丙基异氰脲酸酯的吸附性能简

用静态吸附法考察粉末活性炭对水中三烯丙基异氰脲酸酯（CAIC）的吸附行为,采用单因素分析法对活性炭吸附化工废水中TAIC的工艺条件进行研究。实验结果表明,在TAIC模拟废水中,其TAIC初始浓度为800 mg/L,pH为7,在温度为298 K、转速为150 r/min的条件下,当活性炭的投加量达到4.4 g/L,吸附反应时间为50 min时,TAIC的去除效率最高为96.17%;对于实际废水,其TAIC初始浓度为1 500 mg/L,溶液pH为3,在温度为298 K、转速为150 r/min的条件下,当活性炭投加量达到10 g/L,吸附反应时间为2 h时,TAIC的去除效率最高为46.8%。这也是由于实际废水组分复杂,其他有机物存在一定的吸附竞争机制。     

溶解性有机碳对微库仑法测定水中可吸附有机卤素的影响

微库仑法测水样中可吸附有机卤素(AOX)受多种因素影响,其中溶解性有机碳(DOC)的影响非常显著。DOC对微库仑法2种前处理方法(双柱法和振荡法)的影响差异很大。双柱法受DOC影响较小,当DOC浓度小于1 000 mg/L时,AOX加标回收率范围为94.0%~104%。振荡法受DOC影响较明显,随着DOC浓度的升高,AOX回收率持续下降,当DOC浓度达到1 000 mg/L时,AOX加标回收率下降至72.1%,但DOC浓度小于100 mg/L时,AOX加标回收满足方法要求。进一步研究发现,DOC对振荡法的影响主要由于竞争吸附降低了活性炭对AOX的吸附容量,而非吸附速率,虽然增大活性炭用量可在一定程度上减小DOC对AOX测定的影响,但对样品进行稀释是减少DOC影响的最简单高效的办法。同时,DOC对不同类型的有机卤代物影响不同,有机溴受DOC影响程度小于有机氯。     

可溶性有机质对芘在泥炭和高岭土上吸附和解吸的影响

为掌握可溶性有机质(DOM)对憎水性有机污染物吸附和解吸行为的影响,本研究选取四环多环芳烃——芘作为目标污染物,通过批平衡实验研究了不同分子量组分DOM对芘在泥炭和高岭土上吸附和解吸的影响.结果表明,吸附和解吸数据均可以用Freundlich模型很好地拟合(R2＞0.93).DOM的添加抑制了泥炭对芘的吸附,并且分子量...     

无定型纳米TiO2吸附去除饮用水中的低浓度As(Ⅲ)

研究了纳米无定型TiO2颗粒对饮用水中低浓度的三价砷As(Ⅲ)吸附行为。纳米TiO2颗粒吸附剂的BET表面积为205 m2/g,计算的BJH吸附平均孔径为4.02 nm(4 V/A)。对起始As(Ⅲ)浓度为150μg/L的模拟含砷水,经过5h的吸附处理后残余浓度不足4μg/L,As(Ⅲ)去除率达到97%。反应起始阶段吸附速率较快,84%的As(Ⅲ)能够在20min内去除。As(Ⅲ)吸附动力学较好地符合拟二级动力学模式。最佳As(Ⅲ)吸附pH为9.3,低于此值,随酸性增加吸附速率有所降低;而高于此值的强碱性pH对吸附有强烈抑制作用。在平衡浓度较低的情形下(10～220μg/L),Lang-muir,Freundlich和Dubinin-Radushkevich(D-R)吸附等温式均可较好拟合吸附行为,但中性和弱碱性条件下更符合Fre-undlich吸附等温式;平衡浓度大于220μg/L,吸附容量随平衡浓度增加而迅速增加,最大吸附容量在低浓度下达到4.79 mg/g。     

新疆某石化企业污水库周边土壤对钴的吸附行为研究

采用静态吸附法研究了新疆菜石化企业污水库周边土壤对重金属钴的吸附特征,考察了溶液pH值、钴离子平衡质量浓度、背景电解质浓度、吸附时间和环境温度等因素对钴吸附量的影响,并对吸附机理进行了初步探讨.结果表明:溶液pH值为1～4时,改变pH值对土壤吸附钴的影响显著;吸附时间在3h左右时钴吸附量趋于稳定;随溶液背景电解质浓度增大,土壤对钴的吸附量呈现先急剧后缓慢的下降趋势;土壤对钴的吸附量随温度升高而增加.拟合结果表明,Langmuir和Freundlich模型能较好地描述土壤对钴吸附的热力学过程;在3h内,土壤对钴吸附的动力学过程可以用一级反应动力学方程表示.方差分析结果表明,对土壤吸附钴量有显著性影响的因素有溶液pH值、钴离子平衡浓度、吸附时间和温度等.