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排序方式: 共有307条查询结果,搜索用时 23 毫秒
1.
陈以良 《广东海洋大学学报》1992,(1)
用比电导法研究两种活性炭自稀水溶液中吸附强电解质硫酸铬和硫酸铜的吸附平衡特性。结果表明,在本文的研究条件下,两种活性炭对硫酸铬和硫酸铜都有吸附作用。同时,活性炭吸附硫酸铜的吸附平衡特性可以用 Freundlich 方程式来描述。研究的结果对固体在溶液中的吸附基础理论以及处理工业废水具有一定的意义。 相似文献
2.
The uptake and release of trace metals (Cu, Ni, Zn, Cd, and Co) in estuaries are studied using river and sea end-member waters
and suspended particulate matter (SPM) collected from the Changjiang Estuary, China. The kinetics of adsorption and desorption
were studied in terms of environmental factors (pH, SPM loading, and salinity) and metal concentrations. The uptake of the
metals studied onto SPM occurred mostly within 10 h and reached an asymptotic value within 40 h in the Changjiang Estuary.
As low pH river water flows into the high pH seawater and the water become more alkaline as it approaches to the seaside of
estuary, metals adsorb more on SPM in higher pH water, thus, particulate phase transport of metal become increasingly important
in the seaward side of the estuary. The percentage of adsorption recovery and the distribution coefficients for trace metals
remained to be relatively invariable and a significant reduction only occurred in very high concentrations of metals (>0.1 mg L−1). The general effect of salinity on metal behavior was to decrease the degree of adsorption of Cu, Zn, Cd, Co, and Ni onto
SPM but to increase their adsorption equilibrium pH. The adsorption–desorption kinetics of trace metals were further investigated
using Kurbatov adsorption model. The model appears to be most useful for the metals showing the conservative behavior during
mixing of river and seawater in the estuary. Our work demonstrates that dissolved concentration of trace metals in estuary
can be modeled based on the metal concentration in SPM, pH and salinity using a Kurbatov adsorption model assuming the natural
SPM as a simple surfaced molecule. 相似文献
3.
Phosphorus transport in shallow groundwater in peri-urban Kampala, Uganda: results from field and laboratory measurements 总被引:1,自引:0,他引:1
To understand Phosphorus (P) sources and transport processes in the subsurface in Bwaise III Parish, Kampala, P attenuation
and adsorption capacities of soils were studied in situ and from laboratory measurements. Relationships between sorption parameters
and soil matrix properties, rates and mechanism of the adsorption process and soil P fractions were also investigated. P was
generally higher in the wet than the dry season, but for both seasons, the maximum was 5 mgP/l. P transport mechanisms appeared
to be a combination of adsorption, precipitation, leaching from the soil media and by colloids with the latter two playing
an important role in the wet season. The sorption process comprised two phases with the first stage rate constants being about
fourfold those of the second stage. The Langmuir isotherm described the sorption data well (R
2 ≥ 0.95) with the second soil layer exhibiting the highest sorption maximum (C
max) (average value 0.6 ± 0.17 mgP/gDW). The best prediction of C
max had organic carbon, Ca, available P and soil pH. Residual P consisting mostly of organics was the main fraction in all the
layers followed by inorganic HCl-P and NaOH-P in the top and middle layers, respectively. Loosely bound P (NH4Cl-P) was the least fraction (<0.4% of total P) in all layers indicating the high binding capacity of P by the soils. The
study results suggest that P dynamics is related to Ca, Fe and organic carbon content of the soils. 相似文献
4.
水溶液中聚合物在粘土上的吸附对于聚合物污染防治和污水处理等都有重要意义。Scheutjens-Fleer理论是应用范围最广的聚合物吸附理论,适应于从单体到长链高聚物,从链无相互作用的稀溶液到纯聚合物的吸附研究。本文简要介绍了有关聚合物吸附的重要参数,包括吸附量、耦合分数或直接表面覆盖、平均层厚度和链段密度,以及相应的测定方法。文中分析了影响聚合物吸附研究发展的主要问题,指出水溶液中聚合物在粘土上的吸附研究的发展方向是综合研究吸附等温线和A/V效应、耦合分数、吸附层厚度、吸附分级现象和对粘土层间的影响,并与Scheutjens-Fleer理论计算结果进行比较。 相似文献
5.
氨基酸在粘土高岭石上吸附等温线的研究 总被引:2,自引:0,他引:2
研究了4种氨基酸(甘氨酸,赖氨酸,天冬氨酸,谷氨酸)在粘土高岭石上的吸附等温线以及金属铜离子对其等温线的影响。研究表明,氨基酸在高岭石上的吸附等温线以及金属铜离子存在时的吸附等温线均属Langmuir型等温线;铜离子浓度增加时,其等温线斜率也增加,并认为体系可形成Ⅰ型三元表面络合物,铜离子对氨基酸在高岭石上等温线影响的规律和在相同体系中它对氨基酸在高岭石上交换吸附百分率E(%)-pH曲线的影响规律相一致。 相似文献
6.
通过模拟实验制备了硅酸盐类不溶性固体,从X射线衍射特征和红外光谱特征两方面看,制得的硅酸盐类与河口新生相成分,结构相似,表明铁水解成的β-FeOOH胶体吸附Si,Al,Mg,K等元素,经结构重组可形成硅酸盐矿物,这可能是河口体系新生相的形成原因。 相似文献
7.
8.
A. Glabert O.S. Pokrovsky C. Reguant J. Schott A. Boudou 《Journal of Geochemical Exploration》2006,88(1-3):110
This work is devoted to the physico-chemical study of cadmium and lead interaction with diatom–water interfaces for two marine planktonic (Thalassiosira weissflogii = TW, Skeletonema costatum = SC) and two freshwater periphytic species (Achnanthidium minutissimum = AMIN, Navicula minima = NMIN) by combining adsorption measurements with surface complexation modeling. Reversible adsorption experiments were performed at 20 °C after 3 h of exposure as a function of pH, metal concentration in solution, and ionic strength. While the shape of pH-dependent adsorption edge is similar among all four diatom species, the constant-pH adsorption isotherm and maximal binding capacities differ. These observations allowed us to construct a surface complexation model for cadmium and lead binding by diatom surfaces that postulates the constant capacitance of the electric double layer and considers Cd and Pb complexation with mainly carboxylic and, partially, silanol groups. Parameters of this model are in agreement with previous acid–base titration results and allow quantitative reproduction of all adsorption experiments. 相似文献
9.
A. López Valdivieso A.A. Sánchez López C. Ojeda Escamilla M.C. Fuerstenau 《International Journal of Mineral Processing》2006
The role of pH and pulp redox potential (EH) to control the flotation and depression of arsenopyrite has been investigated through studies on microflotation of arsenopyrite crystals and batch flotation of an arsenopyritic ore using isopropyl xanthate as collector. The transition between flotation and depression of arsenopyrite is established by the reversible potential of the xanthate/dixanthogen couple. Adsorption of arsenate ions on ferric hydroxide has been studied through electrokinetics to delineate mechanisms involved in the depression of arsenopyrite using oxidants. Chemical binding between arsenate species and ferric hydroxide sites on arsenopyrite is suggested as the mechanism responsible for depression of arsenopyrite. EH conditions are given for the flotation and depression of arsenopyite at various pH values for the arsenopyritic ore. 相似文献
10.
The effect of phosphate and glutamic acid on adsorption of aluminium onto a latosol was investigated as a function of pH and ligand concentrations through batch equilibrium experiments. The results showed that adsorption of aluminium by the soil was enhanced after addition of phosphate at low pH, and this promotive effect was gradually eliminated with the increase in pH. The positive effect of phosphate on aluminium adsorption onto latosol was attributed to phosphate-induced surface negative charge and formation of ternary surface complexes involving aluminium and phosphate. While using silica as adsorbent, the inactive surfaces for phosphate, promotion of adsorption of aluminium by phosphate was also found. Then it was proposed that additional aluminium might bind to the phosphate adsorbed onto the silica in the form of surface complexes silica–aluminium–phosphate again, and the mechanism might operate in the soil systems as well. Glutamic acid exhibited no influence on the adsorption of aluminium by the soil at low pH. After increasing the pH, adsorption of aluminium was inhibited especially with the highest addition of glutamic acid, probably owing to weak affinity of complexes between glutamic acid and aluminium to the soil. 相似文献