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1.
The adsorption of Cu, Pb, and Zn by synthetic goethite was studied in the absence and presence of oxalic, citric, and glutamic acids at different pH values. It was shown that, in the absence of an acid, the content of adsorbed metals increased with the increasing pH. The content of adsorbed cations at constant pH values decreased in the sequence: Cu > Pb > Zn. The simultaneous addition of metal cations and organic acids to the goethite suspension increased the content of the adsorbed elements. The oxalic and citric acids had similar effects on the adsorption of copper and lead in the studied pH range. The metal: acid concentration ratios significantly affected the adsorption of the heavy metals by goethite. An increase in the metal adsorption was observed to a certain metal: acid ratio, which was followed by a gradual decrease. The adsorption of the metals by goethite also depended on the properties of the metal cations and the organic ligands. The observed tendencies were attributed to the complexation of heavy metals with organic acid anions and the simultaneous sorption of acids at positively charged sites on the goethite surface with the formation of mineral-organic compounds, which significantly modified the surface properties of the mineral. The study of the effect of increasing lead concentrations in the solution on the copper adsorption by goethite in the absence, in the presence, and at the addition of an oxalic acid solution to the goethite suspension one hour before the beginning of the experiment showed that lead decreased the adsorption of copper in all the treatments. The possible mechanisms of the processes occurring in the system were considered.  相似文献   

2.
有机酸对高岭石, 针铁矿和水铝英石吸附镉的影响   总被引：12，自引：0，他引：12  
LIAO Min 《土壤圈》2006,16(2):185-191
Effects of organic acids （oxalic, acetic, and citric） on adsorption characteristics of Cadmium （Cd） on soil clay minerals （kaolinite, goethite, and bayerite） were studied under different concentrations and different pH values. Although the types of organic acids and minerals were different, the effects of the organic acids on the adsorption of Cd on the minerals were similar, i.e., the amount of adsorbed Cd with an initial solution pH of 5.0 and initial Cd concentration of 35 mg L^-1 increased with increasing concentration of the organic acid in solution at lower concentrations, and decreased at higher concentrations. The percentage of Cd adsorbed on the minerals in the presence of the organic acids increased considerably with increasing pH of the solution. Meanwhile, different Cd adsorption in the presence of the organic acids, due to different properties on both organic acids and clay minerals, on kaolinite, goethite, or bayerite for different pHs or organic acid concentrations was found.  相似文献   

3.
Adsorption, desorption, and precipitation reactions at environmental interfaces govern the bioavailability, mobility, and fate of organic phosphates in terrestrial and aquatic environments. Glycerophosphate (GP) is a common environmental organic phosphate, however, surface adsorption reactions of GP on soil minerals have not been well understood. The adsorption characteristics of GP on goethite were studied using batch adsorption experiments, zeta (ζ) potential measurements, and in situ attenuated total reflectance‐Fourier transform infrared spectroscopy (ATR‐FTIR). GP exhibited fast initial adsorption kinetics on goethite, followed by a slow adsorption. The maximum adsorption densities of GP on goethite were 2.00, 1.95, and 1.44 μmol m?2 at pH 3, 5, and 7, respectively. Batch experiments showed decreased adsorption of GP with increasing pH from 3 to 10. Zeta potential measurements showed a remarkable decrease in the goethite isoelectric point upon GP adsorption (from 9.2 to 5.5), suggesting the formation of inner‐sphere surface complexes. In addition, the ATR‐FTIR spectra of GP sorbed on goethite were different from those of free GP at various pH values. These results suggested that GP was bound to goethite through the phosphate group by forming inner‐sphere surface complexes.  相似文献   

4.
ADSORPTION OF THE HERBICIDE 2,4-D ON GOETHITE   总被引：1，自引：0，他引：1  
Adsorption, of the herbicide 2,4-Dichlorophenoxyacetic acid (2,4-D) on an iron oxide, goethite, was studied in aqueous suspensions as a function of solution pH, ionic strength of the medium, and initial 2,4-D concentration. The 2,4-D anion was reversibly adsorbed on positively charged goethite surfaces, maximum adsorption being observed near the pKa of 2,4-D (2.73) and at low ionic strength. Within certain levels of adsorption (5–22 mg 2,4-D adsorbed/g goethite) the complex became hydrophobic and floated to the liquid surface. This flotation effect disappeared on further adsorption. It is suggested that adsorbed 2,4-D anions are orientated with their hydro-phobic aromatic ends directed towards the solution, the carboxyl groups being weakly bound to positive sites on the oxide surface. At high levels of adsorption, some of the anions are orientated in the opposite direction by π–π interaction, with the first adsorbed layer and the surface reverts to its hydrophilic nature.  相似文献   

5.
硼的吸附-解吸对土壤表面性质的影响   总被引：5，自引：1，他引：5  
对三种不同类型土壤———棕红壤、黄棕壤、灰潮土在特定条件下的电荷零点(PZC) :ck—PZC(无硼 )、ads—PZC(硼吸附 )和des—PZC(硼解吸 )的研究发现 ,棕红壤和黄棕壤的ads—PZC与其ck—PZC相比 ,都有较为明显的下降。灰潮土 ,由于本身碳酸盐的缓冲作用 ,其ads—PZC与ck—PZC几乎相等。在硼吸附发生后 ,3种供试土壤的des—PZC较之它们的ads—PZC ,改变甚小 ,但这时灰潮土却保持强劲吸附电位离子的趋势 ,其吸附H 离子数量是棕红壤和黄棕壤的 2倍 ,表明在灰潮土上 ,原先被土壤胶体吸附的硼这时才显示利于电位离子的吸附。研究还表明 ,硼在酸性土壤中的吸附会引起 1 0倍量的质子的吸附  相似文献   

6.
用吸附平衡法研究了不同草酸浓度、体系pH对针铁矿 (G)吸附Cd2+的影响与机制以及电解质 (KNO3)浓度对针铁矿、草酸化针铁矿 (G+40 )吸附Cd2+的影响差别及原因。结果表明 ,低浓度草酸 (1mmolL-1 )促进Cd2+的吸附 ;高浓度草酸 (1mmolL-1/sup )抑制Cd2+的吸附。已吸附在针铁矿表面的草酸对Cd2+ 吸附的影响与液相中草酸的影响不同 ,这主要与草酸引起的针铁矿表面电荷性质的变化、草酸在固液两相间的分配、草酸与Cd2+的配合作用和竞争作用有关。电解质 (KNO3)浓度对针铁矿和草酸化针铁矿吸附Cd2+的影响明显不同 ,随KNO3 浓度的提高 ,针铁矿的Cd吸附率由 44.5%增至 95%以上 ,而草酸化针铁矿吸附率由 29%降至6.2% ,这主要决定于二者的电荷零点 (PZC)和体系pH变化的不同。  相似文献   

7.
ADSORPTION ON HYDROUS OXIDES I. OXALATE AND BENZOATE ON GOETHITE   总被引：3，自引：0，他引：3  
The adsorption of oxalic acid on synthetic goethite (α-FeOOH) was studied using adsorption isotherms. Infrared spectra were obtained for goethite-oxalate complexes at several points on the isotherms. On a goethite preparation with a phosphate sorption capacity of 200|μmolg?1 the amounts of oxalate strongly adsorbed varied from near zero at pH 8 to about l00μmolg?1 at pH 4 and below. At pH 3.4, the first l00μmolg?1 of oxalic acid added was strongly adsorbed as a binuclear complex (FeOOC–COOFe), replacing two singly-coordinated OH groups by ligand exchange. At higher concentrations a further 200 μrnol g?1 of oxalic acid formed a monodentate complex (FeOOC–COOH) so that more oxalate could be accommodated. Benzoic acid was weakly adsorbed on goethite with one benzoate oxygen replacing one singly-coordinated OH. The other oxygen of the COO group fitted into the goethite surface so that the benzene ring was at a high angle to the (100) face.  相似文献   

8.
HU GUO-SONG 《土壤圈》1994,4(2):153-164
The study results of the effects of temperature and ionic strength on the adsorption kinetics of Pb2+ and Cu2+ by latosol, red soil and kaolinite coated with Mn oxide showed that Pbr" and Cur" adsorption by all samples, as a whole, increased with raising temperature. Temperature also increased both values of Xm (the amount of ion adsorbed at equilibrium) and k (kinetics constant) of Pb2+ and Cu2+ The activation energies of Pb2+ adsorption were kaolin-Mn>red soil>goethite and those of Cu2+ were latosol>red soil>kaolin-Mn>goethite. For a given single sample the activation energy of Cu2+ was greater than that of Pb2+. Raising ionic strength decreased the adsorption of Pb2+ and Cu2+ by latosol, red soil and kaolinite coated with Mn oxide but increased Pb2+ and Cu2+ adsorption by goethite. The contrary results could be explained by the different changes in ion forms of Pb2+ or Cu2+ and in surface charge characteristics of latosol, red soil, kaolin-Mn and goethite. Increasiclg supporting electrolyte concentration in-creased Xm and k in goethite systems but decreased and k in kaolin-Mn systems. All the timedependent data fitted the surface secondorder equation very well.]  相似文献   

9.
Extracellular enzymatic activities in soils are essential for the cycling of organic matter. These activities take place in multiphase environments where solid phases profoundly affect biocatalytic activities. Aspergillus niger is ubiquitous in soils; its β-glucosidase plays an important role in the degradation of cellulose, and therefore in the global carbon cycle and in the turnover of soil organic matter. However, the information on the interactions of this protein with soil minerals is very limited, and even less is known about their consequences for the hydrolysis of the natural substrate cellobiose. We therefore characterised the sorptive interactions of this enzyme with the soil minerals montmorillonite, kaolinite and goethite and quantified the resulting changes in the hydrolysis rate of cellobiose. Fractions of adsorbed protein, and the resulting catalytic activity loss, were lower for montmorillonite than for kaolinite and goethite at given experimental conditions; adsorption was 9.7 ± 7.3% for montmorillonite, 70.3 ± 3.1% for kaolinite and 71.4 ± 1.8% for goethite, respectively. Adsorption of the protein to the minerals caused a total decrease in the catalytic activity of 18.8 ± 3.4% for kaolinite and 17.9 ± 4.7% for goethite whereas it was not significant for montmorillonite. The average catalytic activity lost by the pool of adsorbed molecules was 26.8% for kaolinite and 25.0% for goethite. Both the amount of adsorbed protein and the resulting loss of catalytic activity were found to be independent of the specific surface areas yet were influenced by the electrical properties of the mineral surfaces. Under the experimental conditions, montmorillonite and kaolinite are negatively charged whereas goethite is positively charged. However, because of the adsorption of phosphate anions from the buffer, a charge reversal took place at the surface of goethite. This was confirmed by zeta (ζ)-potential measurements in phosphate buffer, revealing negative values for all the tested minerals. Indeed goethite interacted with the enzyme as a negatively charged surface: the amount of adsorbed protein and the resulting catalytic activity loss were very similar to those of kaolinite. Our results show that, even if an important fraction of β-glucosidase is adsorbed to the minerals, the catalytic activity is largely retained. We suggest that this strong activity retention in presence of soil minerals results from a selective pressure on A. niger, which benefits from the activity of the adsorbed, and thus stabilized, enzyme pool.  相似文献   

10.
The adsorption of a mixture of 16 isotopes of 14 rare earth elements (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) present in the initial solution in equal concentrations by quartz and goethite in the presence of bacteria Rhodopseudomonas palustris was studied under different acidity conditions. The solution pH was apparently the leading factor in the interaction of rare earth ions with the surface of mineral and biological sorbents. These interactions were controlled by electrostatic forces in acid (pH 4) and neutral (pH 7) solutions; the precipitation of elements from the solution was the predominant mechanism under alkaline conditions (pH 9). Microorganisms affected the adsorption of lanthanides by quartz in the entire pH range under study, especially at pH 7. In the presence of bacteria, the adsorption of the elements studied by goethite increased in an acid solution, remained unchanged under neutral conditions, and slightly decreased under alkaline conditions. Microorganisms increased the concentration of nonexchangeable forms of the elements adsorbed on the surface of quartz and goethite, which could be due to the formation of low-soluble complexes of rare earth elements with organic substances produced by bacteria.  相似文献   

11.
镉与柠檬酸、EDTA在几种典型土壤中交互作用的研究   总被引：28，自引：4，他引：28  
采用批平衡实验方法研究了镉在青黑土 (IB)、黄棕壤 (YB)和红壤 (R)三种土壤上的吸附和解吸过程以及吸附介质酸度、共存有机酸等对此过程的影响。结果表明 :柠檬酸、EDTA的存在明显降低了镉在黄棕壤和青黑土上的吸附 ,同时镉解吸率较在硝酸钠体系要小 ,有机物的存在增加了土壤中镉的相对非饱和吸附点位。而在红壤上有机物的存在对镉的影响则随介质pH的改变而发生显著变化。酸性条件下 ,有机物的存在增加镉在红壤上的吸附 ,而随pH的增加 ,有机物减少镉的吸附。同时镉在硝酸钠体系中的解吸率随总吸附量的增加而呈现峰形的变化规律。土壤类型变化显著影响镉与有机物之间的交互作用过程  相似文献   

12.
The herbicide glyphosate and inorganic phosphate are strongly adsorbed by inorganic soil components, especially aluminium and iron oxides, where they seem to compete for the same adsorption sites. Consequently, heavy phosphate application may exhaust soil's capacity to bind glyphosate, which may lead to pollution of drain‐ and groundwater. Adsorption of phosphate and glyphosate to five contrasting Danish surface soils was investigated by batch adsorption experiments. The different soils adsorbed different amounts of glyphosate and phosphate, and there was some competition between glyphosate and phosphate for adsorption sites, but the adsorption of glyphosate and phosphate seemed to be both competitive and additive. The competition was, however, less pronounced than found for goethite and gibbsite in an earlier study. The soil's pH seemed to be the only important factor in determining the amount of glyphosate and phosphate that could be adsorbed by the soils; consequently, glyphosate and phosphate adsorption by the soils was well predicted by pH, though predictions were somewhat improved by incorporation of oxalate‐extractable iron. Other soil factors such as organic carbon, the clay content and the mineralogy of the clay fraction had no effect on glyphosate and phosphate adsorption. The effect of pH on the adsorption of glyphosate and phosphate in one of the soils was further investigated by batch experiments with pH adjusted to 6, 7 and 8. These experiments showed that pH strongly influenced the adsorption of glyphosate. A decrease in pH resulted in increasing glyphosate adsorption, while pH had only a small effect on phosphate adsorption.  相似文献   

13.
土壤对铜离子的专性吸附及其特征的研究   总被引：24，自引：4，他引：24  
武玫玲 《土壤学报》1989,26(1):31-41
供试土壤专性吸附铜的等温线均符合Langmuir方程。红壤吸附量最低,砖红腹与黄泥土最大吸附量相近,但在铜浓度低时砖红壤吸铜量远低于黄泥土,而在高浓度则反之。土壤专性吸附铜是在溶液中Na+浓度比Cu2+高8.3—100倍条件下,Na+离子仍不足以与之竞争的那些专性吸附点所吸持的铜。按其解吸条件区分为松结合铜(可为N NH4Cl解吸)和紧结合铜(仅能为0.1 N HCl解吸)两种。紧结合铜受平衡溶液铜浓度影响很小,所占据的吸附点对Cu2+有较强亲和力。松结合铜则随平衡铜溶液浓度增大而增加,符合Langmuir方程。对于砖红壤和黄泥土,在铜浓度低时紧结合铜>松结合铜;浓度高时则反之。红壤专性吸附铜始终以松结合铜为主。三种土壤比较,紧结合铜是砖红壤>黄泥土>红壤;松结合铜则是黄泥土>砖红壤>红壤。造成这些差别的原因可能与土壤性质、氧化物、有机质和粘土矿物组成等不同有关。用平衡法研究三种土壤专性吸附铜在不同浓度NH4Cl和HCl溶液中的解吸表明,可进一步区分为三或四种不同的结合状况。红壤对铜吸附容量最小,且最易解吸。  相似文献   

14.
根瘤菌存在下土壤胶体和矿物对镉的吸附   总被引：8，自引：2，他引：6  
Experiments were conducted to study the adsorption of Cd on two soil collids(red soil and yellowbrown soil) and three variable-charge minerals (goethite,noncrystalline Fe oxide and kaolin) in the absence and presence of rhizobia.The tested strain Rhizobium fredii C6,tolerant to 0.8 mmol L^-1 Cd,was selected from 30 rhizobial strains.Results showed that the isotherms for the adsorption of Cd by examined soil colloids and minerals in the presence of rhizobia could be described by Langmuir equation.Within the range of the numbers of rhizobial cells studied,the amount of Cd adsorbed by each system increased with increasing rhizobial cells,Greater increases for the adsorption of Cd were found in red soil and kaolin systems.Rhizobia influence on the adsorption of Cd by examined soil colloids and minerals was different from that on the adsorption of Cu.The presence of rhizobia increased the adsorption affinity of soil colloids and minerals for Cd,particularly for the goethite and kaolin systems.The discrepancies in the influence of rhizobia on the adsorbability and affinity of selected soil colloids and minerals for Cd suggesed the different interactions of rhizobia with various soil components.It is assumed that bacterial biomass plays an important role in controlling the mobility and bioavailability of Cd in soils with kaolinite and goethite as the major colloidal compnents,such as in variable-charge soil.  相似文献   

15.
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16.
有机肥非水溶性分解产物对 铜 、镉吸附及解吸的影响   总被引：9，自引：0，他引：9  
研究了稻草、紫云英和猪粪淹水培养的非水溶性分解产物、两种土壤( 红壤、潮土) 与这 3 种有机肥共同淹水培养后的非水溶性产物( 水溶性物质被除去) 对铜、镉的沉淀、吸附及解吸作 用的影响。 结果表明, 当铜初始浓度为 10-4mol/ L, pH <6 时有机残渣促进铜的沉淀;当 pH >6 时则抑制了铜的沉淀。 当铜初始浓度降为 10-5mol/ L 时, 有机残渣对铜沉淀的促进作用加强。 3 种有机残渣均促进镉的沉淀, 但促进程度比铜低。 与有机肥共同培养的红壤, 在相同的 pH 条 件下, 提高对铜、镉的吸附;在不调节 pH 条件下, 由于有机肥料有提高 pH 的作用, 进一步提高 对铜 、镉的吸附。 与有机肥共同培养的潮土, 在相同的 pH 条件下, 对铜、镉吸附的影响很小;在 不调节 pH 时, 提高了潮土对铜的吸附, 但对镉吸附的影响则较复杂。 上述结果表明, 有机肥的 非水溶性分解产物主要通过提高体系的 pH 值、与铜、镉形成不溶性的络合物而影响铜、镉的吸 附。 与有机物料共同培养的红壤所吸附的铜、镉的解吸率均不同程度降低。  相似文献   

17.
Competition in adsorption between humic acid (HA) or fulvic acid (FA) and phosphate on synthetic goethite, gibbsite and two tropical soils was studied. The results for both goethite and gibbsite showed that HA and FA competed strongly with phosphate for adsorption sites at low pH values. The soils showed a similar result with a reduction in phosphate adsorption resulting from the addition of HA at the pH of the soils. The competition between HA and phosphate at different pH levels is illustrated by comparing the adsorption envelopes for phosphate on goethite, gibbsite and the two soils in the presence and absence of HA. The trends observed may be explained by the relative positions of the maximum buffer-power (buffer capacity) of the organic acids and of phosphoric acid which are shown to lie in different pH ranges.  相似文献   

18.
砂壤中铜的吸附行为及其影响因素研究   总被引：1，自引：0，他引：1  
王涛  刘廷凤  何忠  孙成 《土壤学报》2007,44(1):84-89
研究了果园附近砂壤中Cu的吸附行为，并探讨了pH值及土壤有机质对吸附的影响。结果表明，供试土壤对Cu的吸附行为可用Freundlieh方程拟合，电性吸附态Cu较易解吸；而专性吸附态Cu较难解吸。动力学实验表明，最初4h内的吸附量占总吸附量的60％以上，8h后达到平衡；而解吸在最初30min内占了近80％，2h后可达平衡。低pH值时，H^＋和Cu发生竞争吸附，可明显抑制土壤对Cu的吸附；随pH值的升高，抑制作用减弱，其logKd与pH呈线性正相关；在中性和偏碱性范围，pH值对土壤吸附Cu的影响不大。原土去除有机质后对Cu的分配系数降低了10倍。  相似文献   

19.
The adsorption of 2-(2,4-dichloro-3-methylphenoxy)propanoic acid (DMPA) on the surface horizon of a humus-rich Andosol was examined. To investigate the mechanisms of adsorption, chemically treated Andosols, such as organic matter removed Andosol, organic matter and active metals removed Andosol, and clay minerals of the Andosol, were prepared. Furthermore, humic acid was extracted from the Andosol. The mechanisms of the DMPA adsorption were identified by using those untreated and chemically treated Andosols and the humic acid. The amount of DMPA adsorbed increased with decreasing equilibrium pH value. Active surface hydroxyl groups were identified as the most important soil functional group in DMPA adsorption. The predominant mechanism of DMPA adsorption on the Andosol is a ligand-exchange reaction, in which an active surface hydroxyl on Al and/or Fe is replaced by a carboxylic group of DMPA. A comparative study revealed that the amount of DMPA adsorbed was slightly greater than that of (2,4-dichlorophenoxy)acetic acid (2,4-D), especially at equilibrium pH values below 5. This is because the octanol-water partition coefficient (log Kow) of DMPA in the equilibrium pH range is higher than that of 2,4-D, and SOM participates in the adsorption process through a hydrophobic interaction.  相似文献   

20.
Rape (Brassica napus L.) seedling pot experiments were performed with a red soil treated with goethite which had boron (B) either adsorbed (ad-B-goethite) or occluded (oc-B-goethite). Soil acidity, different forms of manganese in the soils and different elements content of the rape seedlings were determined. It was found that the addition of boron-containing goethite to the soils resulted in increased rape growth, elevated soil pH and decreased exchangeable acidity. Compared with the control, boron-containing goethite elevated the content of exchangeable manganese (Mn) (EXC-Mn), organic matter bound Mn (OM-Mn), reducible oxide Mn (RO-Mn) and residual Mn (RES-Mn) which were difficult to use for plant. Low labile organic matter was significantly correlated with easily reducible oxide Mn (ERO-Mn) (P < 0.01) and RO-Mn (P < 0.05). Middle organic matter and soil pH was significantly (P < 0.05) correlated with RES-Mn. Stepwise regression was used to select the combination of variables that best estimates shoot and root dry weight of rape seedling. Among them, soil pH, EXC-Mn, OM-Mn, RO-Mn and RES-Mn significantly influenced the dry weight of rape seedlings. The addition of boron-containing goethite improved the uptake of iron (Fe), calcium (Ca), magnesium (Mg), and copper (Cu) element and decreased the uptake of Mn and zinc (Zn) element in rape seedling. The results suggested that boron-containing goethite could provide a better soil acidity environment for plant growth; it was also an important agent increasing a part of manganese difficult to use for plant and reducing the activity of soil manganese, which was beneficial to altering rape seedling growth.  相似文献   

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