Sorption of caesium by complex hexacyanoferrates iii. a study of the sorption properties of potassium copper ferrocyanide

Commercially available potassium copper ferrocyanide (KCuFC) has been studied for caesium sorption. An effective capacity of 2.25 ± 0.06 mmol g^?1 can be achieved at a caseium concentration of 0.015m. The presence of 0.82m, magnesium nitrate reduces the effective capacity to 2.04 ± 0.06 mmol g^?1. The cyanoferrate also shows high caesium uptake in various simulated process solutions relevant to the treatment of radioactive wastes. KCuFC also possesses a high selectivity for caesium in high salt concentration solution. However, the cyanoferrate is not stable in acidic solution of pH < 3. Desorption of the sorbed caesium at various nitric acid concentrations has been investigated and it is concluded that caesium is eluted by a chemical reaction step as a consequence of the oxidation of the cyanoferrate.     

Removal of dissolved rhenium by sorption onto organic polymers: study of rhenium as an analogue of radioactive technetium

Technetium (99Tc) is one of the main components of nuclear wastes. Tc characteristics can be predicted by studying rhenium (75Re), one of its chemical analogue, thus avoiding the use of a radioactive element at high concentrations. The objectives of this experimental study was to understand the sorption behavior of Re with natural organic materials in order to define the possible condition of Tc uptake in case where Tc may be transferred into surface or ground waters. As the well-defined organic sorbents we chose chitosan which contains amine -NH2 groups; poly-galacturonic acid (PGA) and poly-styrene sulfonates (PSS) which contain respectively carboxyl -COOH and sulfonate -SO3H groups. Concerning the reaction of Re with PGA or with PSS, no interaction between Re and carboxyl or sulfonate groups was found within the detection limit of this study. Re sorption on chitosan was found to be dependent on ionic strength and pH. We propose that non-specific sorption of perrhenate ion ReO4- via electrostatic interaction takes place at the protonated amine groups NH3+. The polymer-solution interface can be described by the electric diffuse double layer model combined with the Langmuir-Freundlich model. The calculation is in good agreement with our experimental results.     

D751螯合树脂吸附铀酰,铜,镍,锌及钴的研究

本文研究了国产的具有亚胺二乙酸功能基的大孔螫合树脂D751对铀酰、铜,镍、锌、钴等5种二价离子的吸附性能。测定了树脂对5种二价离子的吸附量与溶液pH值的关系曲线;测定吸附有二价离子的树脂的红外光谱及螯合物解离pH值(DpH)。     

Modern hybrid sorbents – New ways of heavy metal removal from waters

The possibility of hybrid ion exchanger (HIX) application in the simultaneous removal of heavy metal ions such as Cr(VI), Cu(II) and Zn(II) as well as Cd(II) and Pb(II) was presented. The ion exchanger in question combines the unique properties of hydrated metal oxides with the mechanical and thermal stability of synthetic ion exchangers. The kinetics of the sorption process of Cr(VI), Cu(II) and Zn(II) as well as Cd(II) and Pb(II) in the presence of Cl⁻, NO₃⁻ and SO₄²⁻ as well as EDDS (ethylenediaminedisuccinic acid) was also analyzed. Additionally, the effect of initial concentration, phase contact time and pH was also studied. Taking into account the possibility of its application on a large scale, the parameters of the adsorption process were estimated based on the linear form of the Langmuir and Freundlich isotherms.     

INTERFACIAL ADSORPTION OF 2-HYDROXY-5-NONYLBENZOPHENONE OXIME IN STATIC AND VIGOROUSLY STIRRED DISTRIBUTION SYSTEMS

ABSTRACT

The interfacial adsorption of 2-hydroxy-5-nonylbenzo-phenone oxime (LIX65N) at a n-heptane/water interphase was examined under static and vigorously stirred conditions, varying the aqueous pH from 2 to 12. In static systems, the pH and the concentration dependences of the interfacial tension were analysed on the basis of the Gibbs equation. The acid dissociation equilibrium at the interface was evaluated. In vigorously stirred systems, the interfacial adsorption was observed as a reversible, reproducible decrease of the organic phase concentration in response to stirring. A Langmuir isotherm was applicable for the adsorption of neutral LIX65N in acidic condition. The greater adsorption of the anionic form of LIX65N occurring in alkaline condition required an alternative isotherm.     

Plasma grafting montmorillonite/iron oxide composite with β-cyclodextrin and its application for high-efficient decontamination of U(VI)

β-Cyclodextrin (CD) was grafted onto montmorillonite/iron oxides to prepare a novel magnetic CD/MMT/iron oxide composite by low-temperature plasma technology, and applied to remove U(VI) from aqueous solutions. The sorption irreversibility was attributed to inner-sphere binding of U(VI) on CD/MMT/iron oxide surface sites. The thermodynamic parameters indicated that the sorption of U(VI) on CD/MMT/iron oxide was an endothermic and spontaneous process. The maximum sorption capacity of U(VI) on CD/MMT/iron oxide was considerably higher than that of U(VI) on other reported materials. The CD/MMT/iron oxide can be potentially used as a cost-effective material for the purification of actual U(VI)-bearing effluents.     

AN EXPERIMENTAL EVALUATION OF THE GOVERNING MOISTURE MOVEMENT PHENOMENA IN THE PAPER COATING PROCESS. II. EXPERIMENTAL

This paper investigates the moisture movement in the paper coating process experimentally and theoretically. The experimental data is obtained by coating a base paper with a laboratory coater and by scraping off some of the coating color after a certain amount of time. The moisture content of the material, which has been scraped off, is measured and the amount of liquid absorbed from the coating color by the base paper is determined. The laboratory results are similar to measurements made on a pilot-coating machine. The mathematical solution is based on the diffusion of water vapor in air and taken the vapor partial pressure in a hygroscopic material, i.e. paper. The measurements and a theory based on vapor diffusion show that the moisture content of the base paper is an important parameter when trying to determine the loss of water from the coating color to the base paper. This kind of dependency cannot be explained by theories based on water movement in the liquid phase by capillary suction, as is discussed in Berg et al., 2000, Part I: Theoretical Aspects.     

Electrokinetic removal of 2,6-dichlorophenol and diuron from kaolinite and humic acid-clay system

This paper presents the results of a study on the electrokinetic treatment of kaolinite and humic acid kaolinite complexes spiked with 2,6-dichlorophenol or 3-(3,4-dichlorophenyl)-1,1-dimethylurea (diuron). In particular, the attention was paid to the interaction between solid surface and dissolved organics: the effects of contaminant sorption as well as the physicochemical reactions on the efficiency of electrokinetic remediation were investigated. Using a 3V/cm voltage gradient, approximately 90% of diuron was removed from kaolinite after one water pore volume was collected in the cathode reservoir, but much lower efficiency was obtained in the electrokinetic removal of this compound from humic acid-coated kaolinite. The results also showed that partial degradation of the contaminant occurred during electrokinetic treatment of kaolinite clay spiked with 2,6-dichlorophenol: the contamination in the clay could be remediated by the combination of electrokinetic extraction and electrochemical reactions.     

Quaternized Poly(4-Vinylpyridine) Coated Activated Carbon: Diffusion Controlled Sorption of Chromium(VI)

Quaternized poly(4-vinylpyridine) coated activated carbon has been proven to be successful in removal and recovery of Cr(VI) from aqueous solution. However, the key component of the mass transfer operations and the diffusion coefficient has not been determined. In this study, adsorption of Cr(VI) was investigated at different initial concentrations. A finite bath diffusion control model with changing bulk concentrations was derived analytically, and a constant related to radius of the absorbent particle and the fractional attainment of adsorption was first introduced into this model. Results indicated that the adsorbent provided fast adsorption kinetics and the modified diffusion-control model fitted the experimental data well. The observed sorption kinetics was consistent with the finite bath diffusion, with an average value of 4.10×10?6?cm2/s for the product of the distribution coefficient and the effective diffusivity in the adsorption of Cr(VI) on the quaternized poly(4-vinylpyridine) coated activated carbon.     

裂片核素在岩石中的迁移研究 Ⅰ.核素~(75)Se在花岗岩和石灰岩中的扩散行为

高水平放射性废物处置的主要方法是深埋在地质岩石中。在研究放射性核素随地下水穿过岩石缝隙网的迁移中,扩散法起着重要的作用。本文测定了~(75)SeO_3~(2-)在花岗岩和石灰岩(取自北京郊区)中的扩散系数,并详细叙述了实验技术和分析方法。