活性炭吸附-微波诱导氧化处理有机废水

研究了化工废水中有机污染物在颗粒活性炭(GAC)上的吸附行为,以及用微波辐照再生活性炭使污染物被诱导氧化的过程.结果表明,污染物在GAC上的吸附动力学为一级过程,修正后的Freundlich吸附等温线模型能更好地定量描述其吸附过程.再生后活性炭的碘值可以达到900mg·g-1左右,且能耗相对较低.     

电子束辐照下饱和活性炭的再生技术

采用电子束辐照技术,对吸附炸药废水的饱和活性炭进行再生处理.研究结果表明,湿润状态下活性炭辐照再生后的吸附性能明显好于干燥状态.饱和活性炭保持湿润状态,同样剂量下氮气氛辐照比空气氛和真空下辐照再生后碘吸附值和比表面积较大.辐照200 kGy后活性炭的碘吸附值和比表面积分别为未用的新鲜活性炭的97.9%和99.0%,吸附性能在辐照再生后损失较小.     

微波诱导改性活性炭催化处理低浓度抗生素废水

通过采用负载FeSO4活性炭、CuSO4活性炭和一般活性炭作为微波催化剂处理抗生素废水的对比实验,研究不同负载方法对抗生素制药废水COD去除的差别,结果表明,负载FeSO4的活性炭作为催化剂的微波处理系统对COD的去除率最高.以微波诱导负载FeSO4的活性炭为催化剂对抗生素制药废水进行处理,结果表明,增大负载FeSO4活性炭质量,微波辐射时间和微波功率,均有利于抗生素废水中COD的去除,但各影响因素的取值并不是越大越好.对微波诱导负载FeSO4活性炭催化工艺处理抗生素废水进行反应动力学分析,结果显示,过程近似一级反应,其动力学方程为:lnC0/C=0.1413t+5.4121,r=0.9876.反应动力学常数为0.1413 min－1.     

活性炭辅助微波热解污泥反应条件的试验研究

针对微波不能直接实现原污水污泥高温热解的问题,采用活性炭作为微波能吸收物质辅助污泥热解。对影响污泥热解效能的3个主要因素：污泥样品量、活性炭掺杂量和微波辐射功率,各做了3个水平的考察,得到了试验条件下的最优方案：污泥样品量30g、活性炭掺杂量6g、微波辐射功率1200W。结果表明：在最优试验方案下,污泥能在7min内升至920℃的高温,实现污泥快速、高效热解。通过分析3个因素对污泥热解效能的影响,进一步对最优试验方案下的固体产物吸收微波的性能及用其作为掺杂物辅助微波热解污水污泥的可行性进行了研究,结果表明：固体残渣吸收微波性能良好,可以代替活性炭作为更经济、高效的污泥微波热解辅助材料。     

活性炭的光催化再生机理

通过研究催化剂的改性、再生温度、外加氧化剂对活性炭光催化再生反应速度的影响,结合光催化与活性炭的吸附理论,分析了活性炭的光催化再生机理.研究表明,活性炭的光催化再生由三个准一级反应组成.再生初期,再生反应速度由TiO2光催化降解吸附质的速率决定;反应的第二个阶段由光催化反应速度和吸附质的解吸速度共同决定;再生后期,再生反应速度由吸附质在活性炭上的解吸速率所决定.活性炭表面及其大孔内负载的TiO2是使苯酚降解转化分解为无机物的降解中心.正是由于降解中心的存在及其表面苯酚浓度趋于零的状态,使得已吸附于活性炭孔内的苯酚不断向这个中心扩散,形成活性炭孔内苯酚的浓度差.在浓度差的作用下,扩散作用持续进行,导致活性炭内吸附位的逐步空出,从而实现活性炭的光催化再生.     

微波诱导活性炭氧化降解阳离子红GTL废水的特性

采用微波诱导氧化工艺技术,以活性炭为催化剂,对阳离子红GTL染料废水进行氧化处理,考察了活性炭用量、微波功率、反应时间及染料初始质量浓度对阳离子红GTL去除率的影响,利用SEM/EDS、BET表征了反应前后活性炭的结构及组分变化.结果表明:微波和活性炭具有协同效应;在pH=7.0,活性炭用量4 g,阳离子红质量浓度为50 mg·L-1,微波功率300 W,反应时间4 min的条件下,阳离子红GTL去除率达到99.4%;活性炭的结构与组分影响阳离子红GTL的微波处理效果.     

湿式氧化再生饱和片状活性炭及机理研究

采用湿式氧化装置再生吸附间甲酚饱和片状活性炭,采用标准再吸附实验法测定饱和活性炭的再生效率,确定湿式氧化再生的最佳反应时间和温度.通过总有机碳测定仪和高效液相色谱测得再生过程中总有机碳和间甲酚浓度变化,其中间甲酚浓度由脱附过程和降解过程综合影响.通过高效液相色谱和气相色谱-质谱联用确定活性炭再生过程产物包括：间甲酚降解产物乙酸、丙烯酸以及部分稳定的大分子物质,其中乙酸浓度变化是导致总有机碳变化的主要因素.通过氮气吸附脱附测试可知,再生过程中活性炭表面有部分塌陷.通过程序升温脱附-质谱联用技术得出经过再生处理的活性炭表面氧化官能团的数量有显著增加,其中以羧酸酐类和内酯的增加最为显著,表明再生过程中活性炭表面部分被氧化.通过溶液分析以及表征结果,推测再生过程的反应机理.     

活性炭及不同土壤吸附-超临界CO2再生四氯乙烯的特性

为解决干洗店等清洗行业排放的含四氯乙烯(PCE)三废的环境污染问题,开发一种使用经济、适用、有效且无污染的处理技术,需要收集相关的基础参数.文章研究了活性炭及兰州市三种不同的土壤对水中PCE吸附特性及超临界CO2再生活性炭及土壤萃取回收PCE的特性,结果表明,活性炭与土壤吸附水中PCE达到平衡的时间均为7 d,吸附等温线均可用Freundlich等温式拟合,且有较好的相关性;活性炭与不同土壤对PCE吸附能力差异较大,吸附能力由大到小为活性炭>林土>灌淤土>黄绵土,且土壤的吸附能力与土壤有机质、含水率及pH值关系密切;超临界CO2再生活性炭与土壤回收PCE,分别在35 ℃、20 MPa和60 ℃、20 MPa这样不太苛刻的条件下通过调整S/F值可获得较高的回收率,为PCE的污染治理技术提供理论依据.     

生物可降解络合剂[S,S]-乙二胺二琥珀酸改性蛭石和活性炭及其对Fe（Ⅱ）的吸附性能

提出将Fe（Ⅱ）离子吸附络合稳定于活性炭、蛭石表面,再与H2O2组成新的非均相Fenton反应体系,通过加热、煮沸、干燥等简单的物理方法成功地将螯合剂EDDS（[S,S]-乙二胺二琥珀酸）修饰到蛭石和活性炭表面,对蛭石和活性炭进行改性.主要研究了包括pH、温度、初始浓度、反应时间对材料吸附性能的影响.研究表明,在相同条件下EDDS改性可以提高活性炭和蛭石对Fe（Ⅱ）离子的吸附容量,溶液pH、温度、初始浓度对吸附有较大影响.吸附等温线的拟合结果表明,Fe（Ⅱ）离子在 EDDS 修饰的活性炭和蛭石上吸附行为符合 Langmuir 吸附,其饱和吸附量都有所提高,且具有较大的吸附系数,这是由于修饰在活性炭和蛭石表面的 EDDS 和金属离子形成强烈的络合作用所致.     

活性炭吸附对印染废水生化出水中不同种类有机物的去除效果

染料废水是含有一定量有毒物质的有机废水,具有高COD和高色度.传统的生化方法能够去除纺织印染废水中的大部分有机物,然而出水仍有相当大的色度,因此后续处理是必要的.活性炭是使用最广泛和最有效的吸附剂,能很好地去除色度.本文以印染废水生化出水中的溶解性有机物为研究对象,通过树脂分离技术将印染废水生化出水中的有机物分为4类,采用超滤法测定水样的分子量分布,研究了活性炭吸附对印染废水生化出水中4类有机物的去除效果及水样中不同分子量大小有机物的去除特性.     

Removal of heavy metals from aqueous solutions using activated carbon prepared from Cicer arietinum

Removal of Cu²⁺, Cd²⁺, Pb²⁺, and Zn²⁺ from aqueous solutions by activated carbon prepared from stems and seed hulls of Cicer arietinum, an agricultural solid waste, has been studied. The influence of various parameters, such as pH, contact time, adsorbent dose, and initial concentration of metal ions on removal was evaluated. The activated carbon was characterized by FT-IR spectroscopy, X-ray diffraction, and elemental analysis. Sorption isotherms were studied using Langmuir and Freundlich isotherm models. All experimental sorption data were fitted to the sorption models using nonlinear least-squares regression. The maximum adsorption capacity values for activated carbon prepared from Cicer arietinum waste for metal ions were 18 mg g^?1 (Cu²⁺), 18 mg g^?1 (Cd²⁺), 20 mg g^?1 (Pb²⁺), and 20 mg g^?1 (Zn²⁺), respectively. The Freundlich isotherm model fit was best, followed by the pseudo-second-order kinetic model. Desorption studies were carried out with dilute hydrochloric acid for quantitative recovery of the metal ions and for regeneration of the adsorbent.     

Steam activation,characterisation and adsorption studies of activated carbon from maize tassels

In this paper, steam-produced activated carbon (STAC) from maize tassel (MT) was evaluated for its ability to remove basic dye (methylene blue MB) from aqueous solution in a batch adsorption process. The equilibrium experiments were conducted in the range of 50–300 mg/L initial MB concentrations at 30°C, for effect of pH, adsorbent dosage and contact time. The experimental data were analysed by Langmuir, Freundlich and Temkin isotherm models of adsorption. Freundlich adsorption isotherm was found to have highest value of R²(R²=0.97) compared to other models of Langmuir and Temkin having (0.96 and 0.95 respectively). STAC has a high adsorptive capacity for MB dye (200 mg/g) and also showed favourable adsorption for the dye with the separation factor (R_L<1) for the dye-activated carbon system. The kinetic data obtained were analysed using pseudo first-order kinetic equation and pseudo second-order kinetic equation. The experimental data fitted well into pseudo second-order kinetic equation, as demonstrated by the high value of R².     

Adsorption of benzene and toluene from waste gas using activated carbon activated by ZnCl2

A series of activated carbons with high surface area were prepared from walnut shell using chemical activation with ZnCl2. In this research the carbonization stage was carried out at 500℃. The performance of the synthesized carbons evaluated in adsorption of benzene and toluene from waste gas. The influence of impregnation ratio on the characteristics of synthesized activated carbons as well as their adsorption capacity was investigated. The ratio of activation agent to walnut shell was selected in the range of 0.5-2.0 wt/wt. The synthesized activated carbons were characterized using XRD, SEM, BET and FTIR techniques. The highest activated carbon production yield was obtained at impregnation ratio of 1.5 wt/wt. The XRD analysis illustrated that peaks intensity decreased with increasing impregnation ratio showing that amorphous property of samples was increased. The SEM analysis revealed successful pore development in synthesized activated carbons obtained at high impregnation ratios. The surface area of the activated carbons increased with increasing impregnation ratio and its maximum value reached 2643 m2.g 1 at impregnation ratio of 2/1. FTIR analysis indicated that the relative amount of different acidic surface groups on synthesized carbons was a function of impregnation ratio. Experimental results for benzene and toluene adsorption showed a high potential of employing synthesized impregnated activated carbon for treatment of waste gas. Generally, the amount of VOC adsorbed on the surface was affected by physicochemical properties of synthesized activated carbons.     

Treatment of methylene blue-containing wastewater using microorganisms supported on granular activated carbon under packed column operation

We studied the feasibility of using biological granular activated carbon-packed column in treating methylene blue-containing wastewater. The granular activated carbon with immobilized microbes was packed into a column and fed with 3 liter methylene blue-containing wastewater daily. With initial 1350 mg/l of methylene blue and 1550 mg/l of chemical oxygen demand, it was observed that the colour and chemical oxygen demand removal efficiencies were 99 and 78%, respectively. The high treatment performance of the system could be due to the simultaneous adsorption and biodegradation processes and advantages of immobilized microbes compare to suspended cell system.     

不同林分土壤有机碳密度研究

在全球气候变化背景下,森林土壤有机碳作为土壤碳库的重要组成部分,已成为森林生态系统碳循环研究的重点之一;而森林土壤有机碳在剖面上具有明显的垂直分布差异,根据土壤发生层次特点,分别研究各层土壤有机碳含量分布规律,对于准确确定森林土壤碳储量具有重要意义。2008年7月在北京西山妙峰山林区侧柏（Platycladus orientalis）林、刺槐（Robinia pseudoacacia）林、栓皮栎（Quercus variabilis）林和侧柏、油松（Pinus tabulaeformis）混交林内,分别随机选取3个位置挖土壤剖面,然后根据土壤发生层次性特点,把各剖面划分为四个土层（0～10 cm,10～20 cm,20～40 cm和40～60 cm）,每层用环刀取样测定土壤容重,用土壤袋采集1 000 g的土壤样品,经除杂、风干、过筛等程序后,对土样的有机碳含量和碳密度进行了测定和初步研究。结果表明：4种林分下土壤有机碳平均含量和土壤有机碳密度不同,不同林分土壤0～10 cm有机碳含量和碳密度最高,并且均随土壤深度增加呈降低的趋势;其土壤有机碳密度的大小顺序为：栓皮栎林〉侧柏、油松林〉侧柏林〉刺槐林。4种林分类型0～20 cm土层单位面积有机碳储量占总有机碳储量分别为：栓皮栎林51.1%,刺槐林44.2%,侧柏林43.0%,侧柏、油松混交林37.7%,平均为44.0%。     

几种不同更新的森林群落碳储量结构特征分析

森林更新是维持和扩大森林资源的主要途径,也是森林结构调整、森林可持续经营和构建多功能高效的森林生态系统的过程。在安徽南部的岭南林场,选择了马尾松（Pinus massoniana Lamb）人工林（MP）、杉木（Cunninghamia lanceolata）人工林（CF）、阔叶混交天然次生林（MB）和针阔混交人工次生林（MN）等4种具有典型代表性的森林群落类型,研究了不同更新方式形成的森林群落的碳储量结构特征。结果表明：（1）针阔混交次生林树干生物量密度最大,为（67.32±56.57）mg.hm-2,杉木人工林生物量密度最小,为（43.79±9.13）mg.hm-2,而马尾松树干生物量所占比例最大,为（64.04±1.49）%。阔叶混交次生林碳储量最高,为（126.47±90.75）mg.hm-2;（2）4种群落类型中,阔叶混交林与马尾松群落碳密度最大,分别为95.67和98.21mg.hm-2,杉木群落碳密度最小,为55.41 mg.hm-2。阔叶混交林中的灌木层生物量碳密度最大,为（17.438±24.627）mg hm-2,马尾松林的草本层和枯落层生物量碳密度最高,分别为（1.326±0.431）、（5.517±2.846）mg.hm-2;（3）阔叶混交林群落的地下碳储量最高,为（10.5±9.8）mg.hm-2,群落地下碳储量从大到小的顺序是阔叶混交林〉针阔混交林〉杉木林〉马尾松林。相应的群落地上碳储量从大到小的顺序是阔叶混交林〉针阔混交林〉马尾松林〉杉木林。杉木林根茎比（R/S）最大,为0.21±0.01,杉木林群落中的灌木层根茎比（R/S）最大,为1.61±0.11;（4）在阔叶混交林中,株数密度与乔木层、草本层的碳比例正相关。在杉木林群落中,平均胸径、株数密度与乔木层碳所占比例成负相关。除杉木林群落外,灌木层碳含量之比与胸径及密度等调查因子都呈负相关。     

Removal of Cu（ll） ions from aqueous solution by activated carbon impregnated with humic acid

Humic acid （HA） was impregnated onto powdered activated carbon to improve its Cu（II） adsorption capability. The optimum pH value for Cu（II） removal was 6. The maximum adsorption capacity of HAimpregnated activated carbon was up to 5.98mg.g-1, which is five times the capacity of virgin activated carbon. The adsorption processes were rapid and accompanied by changes in pH. In using a linear method, it was determined that the equilibrium experimental data were better represented by the Langmuir isotherm than by the Freundlich isotherm. Surface charges and surface functional groups were studied through zeta potential and FTIR measurements to explain the mechanism behind the humicacid modification that enhanced the Cu（II） adsorption capacity of activated carbon.     

秸秆不同还田方式对土壤中溶解性有机碳的影响

土壤溶解性有机质及其可利用性与土壤质量密切相关。通过研究秸秆不同还田方式(粉碎还田、覆盖还田、高茬还田)对农田土壤溶解性有机碳的影响,探讨了土壤溶解性有机碳对土壤质量的贡献。水溶性有机碳(WSOC)和热水溶性有机碳(HWSOC)通过冷水和热水提取获得。结果表明:秸秆还田能够增加土壤有机质的含量,影响土壤中水溶性有机碳和热水溶性有机碳的含量。在粉碎还田、覆盖还田、高茬还田处理中,粉碎还田的农田土壤中WSOC和HWSOC的含量比覆盖还田、高茬还田的高,粉碎还田的农田土壤中的WSOC和HWSOC占土壤有机碳的百分比也最高。另外,WSOC和HWSOC与土壤呼吸有很好的相关性(相关系数分别为0.75,0.85)。