鄱阳湖滨岸土壤磷素吸附特征研究

分层采集鄱阳湖近水滨岸土壤进行磷的吸附动力学及等温吸附试验,探讨不同位置滨岸土壤的总磷(TP)含量及其对磷吸附解吸特性的差异。结果表明:不同滨岸带土壤TP差异极显著(F=7. 103,p 0. 01),赣江入湖口滨岸土壤总磷含量显著高于其他滨岸土壤,且0～20 cm土层TP含量(635 mg·kg~(-1))20～40 cm土层(393 mg·kg~(-1))。各滨岸土壤的磷素动力学过程相似:即分为"快速吸附(0～2 h)"、"缓慢吸附(2～24 h)"与"吸附平台( 24 h)"3个阶段,平衡吸附量(Q_e)最大值为216. 0 mg·kg~(-1); Langmuir模型对磷的等温吸附拟合度为0. 951～0. 995,表层土壤最大吸附量(Q_(max))高于下层土壤,饶河(629. 12 mg·kg~(-1))吸附量最大,康山大堤(340. 72 mg·kg~(-1))最小。滨岸表层土壤吸附解吸平衡浓度(EPC0)小于0. 1 mg·L~(-1),磷流失风险较小,东部滨岸土壤对外源磷的缓冲能力优于西南滨岸土壤,最大吸附量与TP呈现极显著正相关。     

巢湖陆向湖滨带常见野生植物对磷缓冲能力的影响

湖泊陆向湖滨带缓冲磷扩散的机制尚未得到充分地研究。系统分析了2011年4~7月巢湖陆向湖滨带5种野生植物的生长状况与根际土不同形态磷的含量和吸附行为。结果表明土壤磷的吸附行为可用Langmuir方程加以描述。与对照相比,艾草和小飞蓬根际土总磷含量明显较低,磷的最大吸附量（Qmax）明显较高,而小蓟和狗尾巴草根际土速效磷含量明显较高,Qmax与磷吸附强度明显较低。植物根与茎长均随季节增加,相应的土壤磷饱和度下降。因此,植物吸收与土壤吸附是陆向湖滨带缓冲磷扩散的重要机制。有机质可通过增加速效磷含量和Qmax值调节土壤磷平衡浓度（EPC0）。小飞蓬和艾草根际土的EPC0值明显较低,磷吸附能力较强。而小蓟和早熟禾根际土的EPC0值明显较高,故易成为向湖泊扩散的磷源     

三峡库区悬移质泥沙对磷污染物的吸附解吸特性

就三峡库区悬移质泥沙对磷污染物的吸附解吸特性从野外同步监测和室内试验研究两个方面展开研究。选取长江干流、嘉陵江和乌江共7个监测断面于2002年和2003进行野外同步监测,测试结果表明：水中的悬移质泥沙对水中各种覆存形态的磷污染物浓度具有显著影响,单位重量泥沙对磷的吸附量与水体总泥沙含量、泥沙粒径有密切关系。采集寸滩断面泥沙对磷酸盐吸附解吸特性进行室内试验研究,并根据Langmuir吸附动力学方程对吸附解吸过程进行了拟合,发现吸附速率常数k随着泥沙粒径的增加而呈递增变化,而磷酸盐初始浓度对k值的影响并不明显,同时,磷酸盐解吸量随着泥沙浓度的增加和粒径的增加呈递减变化,k值随着泥沙粒径的增加而呈递增变化,泥沙浓度对k值的影响不明显。     

原煤及富碳沉积物对疏水性有机污染物吸附解吸研究进展

疏水性有机污染物（HOCs）是环境中具有较大的辛醇/水分配系数(〖WTBX〗Kow〖WTBZ〗)的一类持久性有机污染物（POPs）,吸附解吸过程是环境中HOCs迁移转化的重要途径之一。煤是近年来发现的在土壤及沉积物中非线性吸附特征的重要吸附剂之一,通过阐述原煤及富碳沉积物对HOCs吸附解吸机理,并重点分析影响原煤及富碳沉积物对HOCs吸附解吸过程的因素,包括吸附剂和吸附质本身,pH值、盐度和离子强度等环境因子,试途探究煤对HOCs吸附解吸的本质。由于煤的有机质含量、有机碳组成和空间结构等物理化学性质都明显不同于天然土壤和沉积物,因而对HOCs的吸附解吸过程也具有特殊性（如吸附过程一般为非线性,解吸过程的滞后性）。有关煤对HOCs的吸附解吸机理在微观分子角度的探讨、煤与吸附解吸过程中其他影响因子对反应体系的影响、煤对HOCs降解的环境风险评价等的研究还较少,今后需加强对这些方面的研究     

风干和淹水过程对巢湖流域土壤和沉积物磷吸附行为的影响

巢湖湖滨带土壤和沉积物经历明显的干湿交替过程,其磷的迁移和转化方式亦有明显变化。风干作用能显著降低沉积物磷最大吸附量、提高吸附能并增加磷平衡浓度,从而对磷的吸附能力产生不利影响。淹水过程对土壤最大吸附量的影响取决于有机质的损失情况,好氧条件下有机质损失小,磷最大吸附量无明显变化,吸附能增强,磷释放量略有增加;而厌氧条件下土壤有机质含量与磷最大吸附量均显著降低,吸附能明显减小,磷释放量显著升高。因此湖滨带消落区干湿交替将明显促进底质生物可利用性磷的大量释放。在巢湖流域常见的土壤类型中,红壤对磷的缓冲能力最强。向底质中添加氯化铁和硝酸钙可有效控制磷释放,提高磷缓冲能力,增强底质对磷的保持和固定     

川中丘陵县域土壤pH空间变异及影响因素分析——以四川仁寿县为例

利用2012年在仁寿县采集的555个表层土样(0~20cm),应用地统计学方法分析了该县域尺度表层土壤pH值的空间变异特征;并采用方差分析和回归分析量化主要影响因素对土壤pH值空间变异的影响程度。结果表明:研究区土壤pH值在4.02~8.14之间,平均为6.80,总体上以中性和碱性土壤为主;变异系数为14.48%,属中等程度的空间变异性。地统计分析表明,研究区土壤pH值变异函数的最佳理论模型为球状模型,具有中等程度的空间自相关性,且空间自相关范围较大。方差分析和回归分析表明,土壤类型、成土母质和土地利用方式是显著影响土壤pH值的主要因素。其中,成土母质和土地利用方式分别能独立解释76.2%和4.8%的土壤pH值空间变异。土壤类型的解释能力与分类级别有关,土类、亚类和土属可分别独立解释41.3%、57.3%和83.7%的土壤pH值空间变异,因而能反映成土过程和母质特性的土属是研究区土壤pH值空间变异的主控因素。研究结果可为川中丘陵县域尺度土壤pH空间变异分析及区域生态环境管理与建设提供有益参考。     

长江中游平原湖区人工林枯落物和表层土壤持水特性

研究长江流域平原湖区人工林的水源涵养功能,对长江两岸造林绿化和生态修复具有重要指导意义.通过野外调查,采用室内浸泡法,分析比较了7种不同林分类型枯落物层和土壤表层的水源涵养能力.结果表明:(1)枯落物半分解层蓄积量大于未分解层,未分解层蓄积量以池杉林(Taxodium ascendens)最大,半分解层蓄积量以苏柳林(Salix jiangsuensis)最大.池杉林的总蓄积量最大,为3.90 t/hm2;(2)未分解层最大持水率大于半分解层,其值分别为263.63％～530.86％和209.17％～277.91％.未分解层和半分解层的最大持水量为0.95～4.48和4.15～6.02t/hm2,分别以池杉林和苏柳林最大;(3)未分解层有效拦蓄量为0.44～3.11 t/hm2,半分解层为0.75～3.82 t/hm2,分别以池杉林和二球悬铃木林(Platanus acerifolia)最高.总最大持水量和总有效拦蓄量均以池杉林最大,分别为9.61和5.64t/hm2;(4)枯落物持水量随浸水时间的延长表现为先显著增加后减缓,最后达到饱和,两者之间呈对数函数关系.枯落物吸水速率随浸水时间的延长表现为前期吸水速率较大,后急剧变小,最后趋近于0,两者之间呈幂函数关系;(5)表层土壤最大持水量和有效持水量最大的均为苏柳林,分别为1 116.27和213.27t/hm2.枯落物层以池杉林水源涵养能力较好,土壤表层以苏柳林水源涵养能力较好.总体来看,以苏柳林的综合水源涵养能力较好.     

水体悬移质对重金属吸附规律研究——以长江宜昌段为例

随着长江三峡工程的建设 ,上游来水的流速在此减缓 ,随江水而下的大量泥沙在此沉淀 ,将使坝下 (长江中下游 )水中的悬移质浓度降低、粒径改变 ,从而改变水环境容量。利用长江宜昌江段的周年悬移质样及水样 ,研究了悬移质对重金属 (铜、锌、铅、镉及铬 )的吸附特征。结果表明 ,悬移质对上述金属的吸附可用Freundlich型及Langmuir型等温式较好进行拟合 ;当较高浓度的金属污染物排入江水后 ,在吸附及沉淀的共同作用下 ,浓度明显降低 ;单位悬移质的吸附量随悬移质浓度降低而上升 ,但总吸附量降低 ,从而导致水中的金属污染物的平衡浓度升高。所得结果为预测水环境容量提供了依据     

上海城郊土壤重金属含量的空间变异与分布特征

为揭示城市化、工业化等人为活动对土壤环境质量的影响,选择上海城郊结合部为研究区域,采用地统计学方法对表层土壤样品Cu、Zn、Pb、Cr、Mn 5种重金属的空间变异结构和分布特征进行了分析。结果表明：土壤Cu、Cr、Mn、Pb、Zn均属中等变异,土壤Mn含量服从正态分布,土壤Cr、Cu、Pb、Zn含量服从对数正态分布;半方差函数模型拟合结果显示土壤Mn符合指数模型,土壤Cr、Cu、Pb、Zn符合线性模型、其中土壤Cu、Pb、Zn为纯块金效应模型,反映了城郊结合部土壤污染空间变异的复杂性。通过泛克里格插值可直观反应表层土壤重金属含量空间分布特征,发现土壤Cr、Mn呈岛状,土壤Cu、Pb、Zn呈多岛状分布的特点,工业和交通污染源是影响土壤重金属空间分布的重要因素     

“城郊乡”梯度下土壤Cu、Zn、Pb含量的空间变异特征

为揭示城市化、工业化等人为活动对土壤环境质量的影响,选择能反映上海城郊乡梯度差异的中心城区、城郊结合部和远郊,采用地统计学方法对表层土壤样品Cu、Zn、Pb的空间变异结构和分布特征进行了对比分析。结果表明:城市土壤Pb、Cu、Zn的变异系数范围为0.24~0.62,均属中等变异强度。徐汇区土壤Cu、Pb、Zn符合正态分布,闵行区土壤Cu、Pb和Zn符合对数正态分布,奉贤区土壤Zn呈正态分布,土壤Cu、Pb符合对数正态分布。由中心城区到远郊,城市土壤Cu、Pb、Zn的各项统计特征值和变异系数均有较大差异,存在明显的空间分布差异。半方差函数分析结果表明,徐汇区作为中心城区,土壤Cu、Pb、Zn符合球状模型,土壤Cu、Zn具有强烈的空间相关性,土壤Pb具有明显的空间自相关。奉贤区以农业用地为主,土壤Pb符合线性模型,土壤Cu符合高斯模型,土壤Zn符合指数模型,具有强烈的空间相关性。闵行区地处城郊结合部,土壤Cu、Pb、Zn的半方差拟合模型均为线性模型,表现为纯块金形式,以随机变异为主,空间相关性弱。采用Kriging最优内插法进行无偏估值,绘制了表层土壤重金属含量的空间分布图,中心城区、城郊结合部、郊区土壤重金属的空间分布受城市化、工业化、城市交通等因素的影响,均表现出不同的空间分布规律。     

Adsorption and desorption of iodine by various Chinese soils: I. Iodate

In order to assess the adsorption of iodate by different soils from China, a series of batch experiments were conducted. It was found that soils rich in iron oxide had high affinity for iodate. Iodate adsorption isotherms could be well fitted with both Langmuir and Freundlich equations. Iodate adsorption by 20 different soils from China revealed that iodate adsorption was significantly correlated with soil organic matter negatively and positively with free iron oxide contents. At initial concentration of 4 mg I L(-1), iodate adsorption ranged between 9 and 34 mg kg(-1) soil. No correlation between iodate adsorption and cation exchange capacity and soil pH was found. For a single soil, there was a significant linear relationship between the amounts of iodate adsorbed and desorbed, but for a group of different soils, the relationship between the amounts of iodate adsorption and desorption followed a nonlinear relationship, the deviation mainly occurred at high adsorption side. The relationship between K(d) and free aluminum oxide and free iron oxide contents showed an exponential relationship for various soils with exception of the soil from Hetian in Xinjiang.     

三峡库区消落带淹水—落干过程土壤磷吸附—解吸及释放研究

选取三峡库区消落带典型区土壤作为测试土壤，研究了淹水—落干对土壤磷的等温吸附解吸特性，以及土壤吸附一定的磷后再次淹水向上覆水体释磷的规律。研究表明：①三峡库区消落带土壤淹水—落干后吸磷能力增强，由淹水—落干前的256 mg/kg增加到淹水—落干后的625 mg/kg，磷零点吸持平衡浓度（EPC0）由淹水前的0.46 mg/L增加到淹水后的1.47 mg/L；②淹水—落干处理后土壤磷的解吸率降低，由淹水—落干前的73.3%~80.3%降低到67.3%~69.6%；③三峡库区消落带土壤吸附一定磷后，再淹水磷会再次逐渐释放到上覆水当中，且土壤吸附外源磷越多，磷淹水释放强度越大；④ 淹水—落干使吸附一定外源性磷的土壤淹水条件下释放更多的磷。     

Effect of several organic acids on phosphate adsorption by variable charge soils of central China

The effect of several organic acids on phosphate adsorption by acidic soils in subtropical zone of central China was studied. Results showed: (1) citrate and oxalate remarkably reduced the amount of phosphate adsorption, but tartrate, benzoate and acetate had only a very slight influence on phosphate adsorption; (2) the ability of citrate in reducing phosphate adsorption was greater than that of oxalate, moreover, the reduction percentage was dependent on the concentration of organic ligands in the solution; (3) the effect of organic acids on phosphate adsorption was related to the pH value of organic acid solution. The minimum reduction in adsorption of phosphate was present at a specific pH value of organic acid solution which ranged from 2 to 10; (4) a minimum reduction of phosphate adsorption occurred when phosphate was added to the soils before organic acid, whereas a maximum occurred when organic acid was introduced before the addition of phosphate. Meanwhile, the treatment for the mixture of two organic acids resulted in more reduction in phosphate adsorption than each of the organic acids and less than the total of them. Based on these observations, we suggested that the competition between phosphate and organic acids relied on their relatively affinity to soil mineral surface at different conditions.     

Removal of uranium(VI) from aqueous solutions by manganese oxide coated zeolite: discussion of adsorption isotherms and pH effect

This paper discusses the adsorption properties for uranium(VI) by manganese oxide coated zeolite (MOCZ). The removal of uranium(VI) from aqueous solution by adsorption onto MOCZ in a single-component system with various contact times, pH, competitive ions, temperatures and initial concentrations of uranium(VI) was investigated. The experimental results were fitted to the Langmuir, Freundlich and the three-parameter Redlich-Peterson model isotherms to obtain the characteristic parameters of each model. Both the Langmuir and Redlich-Peterson isotherms were found to best represent the measured adsorption data. According to the evaluation using the Langmuir equation, the maximum adsorption capacity of uranium(VI) ions onto MOCZ was 15.1 mg g(-1) at 293K and pH 4.0. Using the thermodynamic equilibrium constants obtained at different temperatures, various thermodynamic parameters, such as DeltaG(0), DeltaH(0) and DeltaS(0), have been calculated. The thermodynamics of uranium(VI) ion/MOCZ system indicates the spontaneous and endothermic nature of the process. It was noted that an increase in temperature resulted in a higher uranium loading per unit weight of the adsorbent.     

Effects of organic acids on copper and cadmium desorption from contaminated soils

A study was conducted to investigate the effect of organic acids on Cd and Cu desorption from natural contaminated soils (NCS) with permanent contamination by metal smelters and from artificial contaminated soils (ACS) derived from an artificial amendment of Cd to three representative zonal soils in Central China. Results showed that the desorption of Cd in either NCS or ACS, with the increment of tartrate or citrate concentration in desorption solution, can be characterized as a valley-like curve. The presence of tartrate or citrate at a low concentration (< or =0.5 mmol/l) inhibited Cd desorption from these two types of soils, whereas the presence of organic acids at high concentrations (> or =2 mmol/l for citrate and about > or =15 mmol/l for tartrate) apparently promoted Cd desorption. The desorption curve of Cu by tartrate solution with different tartrate concentrations can also be characterized as a valley-like curve, while the desorption of Cu in the presence of citrate was directly enhanced with the increment of citrate concentration. With the enhancement of initial pH value from 2 to 8 in the presence of citrate, Cu desorption ratio decreased at the first stage, then increased, and then decreased again. A valley and a peak sequentially appeared in the Cd or Cu desorption curve with initial pH value increment. Compared with citrate, the desorption ratio of Cd or Cu from NCS or ACS was directly decreased in the presence of tartrate, with the enhancement of the pH value from 2 to 8. Cd or Cu desorption was clearly enhanced when the electrolyte concentration of KNO3 or KCl increased in the presence of 2 mmol/l tartrate. Moreover, a higher desorption ratio of Cd or Cu was shown with KCl electrolyte than with KNO3 electrolyte with the same concentration. Based on these observations, we suggest that bioavailabilities of heavy metal can be promoted with selected suitable types and concentrations of organic acid amendment and reasonable field condition.     

The interaction of heavy metals with urban soils: sorption behaviour of Cd, Cu, Cr, Pb and Zn with a typical mixed brownfield deposit

This study investigated the sorption characteristics and release of selected heavy metals (Cd, Cu, Cr, Pb and Zn) from a typical urban soil material from a derelict brownfield site in Western Scotland, UK. The study aimed to evaluate contaminant interactions with an urban substrate, comprising a mix of mineral soil and residue materials (e.g. brick, concrete, wood). This type of material has received little consideration in the literature to date. Soil samples were subject to a sequence of test involving batch equilibration and dynamic leaching, in single (non-competitive) and multi-element (competitive) solutions. The batch experiments were carried out in unadjusted and close to soil field pH conditions (pH 2 and 7, respectively). The equilibrium adsorption capacity for heavy metals was measured and extrapolated using the Langmuir isotherm. The parameters of the isotherms x(m) (the maximum amount adsorbed per unit mass of adsorbent (mg/g)) and b (adsorption constant (m(3)/g)) were calculated for Cd, Cu, Cr, Pb as single-element and multi-element solutions. The adsorption from the single-element solution was more effective than adsorption under multi-element conditions, due to competitive effects. For example, the adsorption of copper from a single-element solution was over four times greater than for a multi-element solution. In the case of Cr and Zn, migration of metal from soil to solution was observed. Adsorption capacity at pH 2 followed the order Cr>Cu>Pb>Cd and at pH 7 Cd>Zn, with precipitation affecting Cu and Pb behaviour. During the column leaching experiment, most of the heavy metals were irreversibly bound to the soil, but in the case of Cr some movement from soil into solution was observed. The results also showed that Cd, Cu, Pb and Zn were removed from the solution and adsorbed on the soil. No significant difference in the metal removal from single- and multi-element solutions was observed. Overall, the urban residue behaved in a similar manner to mineral soils despite a significant component of anthropogenic solid materials.     

Effects of readily dispersible colloid on adsorption and transport of Zn, Cu, and Pb in soils

Soil colloids (<0.002 mm) were extracted from three types of soils to make the colloid-bound forms of Zn, Cu, and Pb solution. The clay mineral types and composition of the colloids, the adsorption characteristics of the colloids, and the effect of readily dispersible colloid on the transport of metals and the quality of the soils and groundwater were studied. The results showed that the adsorption capacity of Cu, Zn, and Pb was greater for the Aquic Vertisols (Shajiang Black soil) as compared to the Udic Luvisols (Brown soil) and Usdic Luvisols (Cinnamon soil), due to the difference of clay content and clay mineral composition in the different soils. The adsorption capacity of Pb was much higher than that of Zn and Cu for the same soils, which would contribute to the chemical properties of metals and specific adsorption characters of the colloids. The mobility of Zn in soils was greater than that of Cu and Pb, while similar trend was found in the transportation processes for Zn and Cu. The concentration of Zn and Cu in leachates increased as the leaching solution volume increased, but the migration of Pb was negligible, and the concentration of Pb could not been detected in leachates even after 7.5 pore volume leaching solution. The influence of mobility on Zn and Cu transport was different for different type of colloids. The mobility caused by readily dispersible colloids from Aquic Vertisols was greater as compared to that of Udic Luvisols and Usdic Luvisols. Analysis of soils after column leaching indicated that Zn was distributed much deeper than Cu, but Pb was almost not migrated, and mainly accumulated in the soil surface. Therefore, Zn had greater tendency for the groundwater pollution than Cu and Pb, and Pb tends to contaminate the surface soils.     

Cadmium desorption in sand

Desorption of cadmium (Cd) from sand was studied by both batch and flow-through methods. Batch experiments were conducted at three pH values (5.5, 6.0 and 6.5). In each case, the amount of Cd desorbed was low compared with the quantity of Cd adsorbed previously. Desorption of Cd in the batch experiments can be described adequately by a Freundlich isotherm. The Freundlich isotherm coefficient, Kf, increased with pH. Hysteresis between the sorption/desorption isotherms was observed in all batch experiments. Flow-through experiments in soil columns were conducted for the same three pH values, with the results used to determine transport and sorption/desorption parameters. Again, the desorption isotherms bore little resemblance to the corresponding adsorption isotherms. The experimental breakthrough curves were well fitted by a nonequilibrium desorption model, however the time scale of the desorption process was much larger than measured in batch experiments. This model was therefore rejected as lacking realism. A simple linear retardation (including hysteresis) model that utilises different isotherms was found to simulate column breakthrough curves well. The Freundlich isotherm coefficients, Kf, in all batch and flow-through desorption experiments were different to values evaluated from the corresponding adsorption experiments. However, in contrast to adsorption, desorption in flow-through experiments was not noticeably affected by changes in pH. The effect of pore-water velocity on desorption was also studied at pH 6.0. No trend was established between flow velocity and the desorption coefficient.