Celtek clay as sorbent for separation-preconcentration of metal ions from environmental samples

The sorption conditions including pH of the aqueous solution, sample volume, etc., on Celtek clay of copper(II), cadmium(II), lead(II), chromium(III), nickel(II) and cobalt(II) ions from environmental samples has been studied. The effects of electrolytes as matrix on the preconcentration were also investigated with the recoveries >95%. The 3 sigma detection limits for copper, cadmium, lead, chromium, nickel and cobalt ions were found to be 0.25, 0.32, 0.73, 0.45, 0.50 and 0.41 microg/l, respectively. The relative standard deviation was <10% for the determination of analytes. The procedure was validated by analysis of a NRCC-SLRS 4 Riverine Water, SRM 1573a Tomato leaves and IAEA 336 Lichen standard reference materials. The developed method was successively utilized for the determination of Cu(II), Cd(II), Pb(II), Cr(III), Ni(II) and Co(II) in various samples including natural waters, wheat and human hair by flame atomic absorption spectrometry (FAAS) with satisfactorily results (recoveries>95% and R.S.D.'s<10%).     

Modified softwood sawdust as adsorbent of heavy metal ions from water

The sawdust of deciduous softwood-poplar, and coniferous softwood-fir, have been found to possess some adsorption capacities for heavy metal ions. Their adsorption capacities can be increased by previous treatment with a sodium hydroxide solution. Adsorption capacities of alkali modified adsorbents were higher than for unmodified ones from 2.5 to 5 times for copper ions, and about 15 times for zinc ions. Also, for modification can be used solution of sodium carbonate, but that alkaline solution is less efficient than sodium hydroxide solution. The 1% sodium hydroxide solution is suggested for modification of softwood sawdust. It was established that the ion exchange is not only adsorption mechanism, than microprecipitation of metal-hydroxide in the pore liquid was happened, too. At the same time, the leaching of organic matters from modified softwood sawdust were less than from unmodified ones for about 7% for poplar and 23% for fir.     

Metal ion complexes of EDTA as solutes for density gradient ultracentrifugation: influence of metal ions

In the study reported here, we study the nature of the metal ion complexes of EDTA as solute systems for analysis of lipoproteins by density gradient ultracentrifugation (DGU) by varying both the complexing metal ion and the counterion. Specifically, the sodium and cesium salts of complexes of Bi/EDTA, Pb/EDTA, Cd/EDTA, Fe/EDTA, and Cu/EDTA were chosen for this study. We show that useful gradients can be formed within a few hours beginning with a homogeneous solution. Data are presented that provide insight into the nature of how these gradients are formed from these complexes and how the selection of a specific complex can be used to enhance particular regions of the lipoprotein density profile for clinical studies. We also examine the use of equilibrium sedimentation theory to correlate the measured density profiles generated by these complexes with their molecular weight.     

Studies on lithium alumino phosphate glasses doped with selenium ions for hard electrolytes

Glass samples of the system (100 − x) (0.5 Li₂O–0.2Al₂O₃–0.3P₂O₅) + xSeO₂ (x is ranging from 0 to 12 mol%, labeled as LAPS _x ) were prepared using the melt quenching technique. FTIR spectral studies indicate that selenium ions mostly occupy network modifying sites due to isolated selenite (SeO₃ ²⁻) groups up to 6 mol% of SeO₂ (LAPS₆) in the LAPS glass network. This has a tremendous effect on the electrical properties. Glass forming ability parameter (K _gl) and the glass transition temperature (T _g) of LAPS samples were characterized by DTA traces. Electrical measurements were carried out as a function of frequency and temperature over the frequency range of 10 Hz to 10⁶ Hz and a temperature range of 303–423 K. The electric modulus formalism was applied to study the relaxation behavior using the impedance data for all the samples at 303 K and also for analyzing the relaxation behavior of the highest conducting sample (6 mol% of SeO₂) at different temperatures. An attempt has been made to relate the measured properties to the structural modifications due to the modifying effect of isolated selenite (SeO₃ ²⁻) groups in the glass network.     

Adsorption of metal ions on lignin

This study investigated the adsorption of the heavy metal ions Pb(II), Cu(II), Cd(II), Zn(II), and Ni(II) on a lignin isolated from black liquor, a waste product of the paper industry. Lignin has affinity with metal ions in the following order: Pb(II)>Cu(II)>Cd(II)>Zn(II)>Ni(II). The adsorption kinetic data can be described well with a pseudosecond-order model and the equilibrium data can be fitted well to the Langmuir isotherm. Metal ion adsorption was strongly dependent on pH and ionic strength. Surface complexation modelling was performed to elucidate the adsorption mechanism involved. This shows that lignin surfaces contain two main types of acid sites attributed to carboxylic- and phenolic-type surface groups and the phenolic sites have a higher affinity for metal ions than the carboxylic sites.     

Production new chelating fibers of polyacrilonitrile for removing metal ions

In this work, raw acrylic fibers (RAF) have been modified with ethanolamine to provide new chelating fibers and prepared polyacrylonitrile‐monoethanolamine (PAN‐MEA). PAN‐MEA fiber was prepared by conversion nitrile groups into hydroxyle groups using ethanolamine solution with different concentration under refluxing at different temperatures and different times. The fiber structure has been investigated by different experimental techniques of characterization such as Fourier transform infrared spectroscopy (FT‐IR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and the physical and mechanical properties has also been investigated in this study. The PAN‐MEA was examined as chelating material in a series of batch adsorption experiments for removal Cu (II), Pb (II) and Ni (II) ions. The ion adsorption of PAN‐MEA was determined with the atomic adsorption method. PAN‐MEA show adsorption metal ions more than usual fiber because of the modification.     

Evaluation of iron-based hybrid materials for heavy metal ions removal

The article presents in detail the results of the sorption of heavy metal ions such as Cu(II), Zn(II), Cd(II), and Zn(II) in the presence of ethylenediamine-N,N′-disuccinic acid as well as chromium(VI) on Purolite Arsen X^np and Lewatit FO36. Factors affecting the sorption equilibrium (sorbent dose, contact time, temperature, pH, and the presence of interfering ions) were studied. To compare the surface morphologies of the studied ion exchangers, scans using atomic force microscope were also recorded, and attenuated total reflectance infrared spectroscopy was applied to establish the adsorption mechanism. The main parameters affecting sorption are initial concentration of the solution, pH, and phase contact time. Temperature has only a slight influence. The kinetic data were fitted using the pseudo-first-order and pseudo-second-order models. In the case of Cr(VI) adsorption, the equilibriums on Purolite Arsen X^np and Lewatit FO36 were established within 60 min, in the case of Cu(II) and Zn(II) within 30–40 min and for Cd(II) and Pb(II) even less than 30 min. Moreover, it was found that the effectiveness of adsorption in the case of Cr(VI), Cu(II), Zn(II), Cd(II), and Pb(II) on Purolite ArsenX^np was higher than that on Lewatit FO36.     

磁性炭包铁纳米粒子对重金属离子的吸附性能

采用氩电弧等离子体法制备炭包铁纳米粒子,并用体积分数30%的H2O2氧化其外层非晶态类石墨碳层,研究炭包铁纳米粒子对水溶液中Cr、Ni、Cd、Pb、Co和Mn等金属离子的吸附和分离特性。结果表明,炭包铁非晶炭层的特殊结构可通过双氧水氧化处理使其表面产生羧基和羟基。在强碱性介质下,羟基和羧基强化了纳米颗粒表面的静电作用,提高了炭包铁对金属离子的吸附性能。当pH值为8.0～10.0时,炭包铁纳米粒子对Cr、Ni、Cd、Pb、Co和Mn的吸附率均超过90%,对重金属离子的吸附能力明显高于活性炭。     

On the role of transition metal elements as structure-stabilising agents in cuprate superconductors

We outline here several key aspects of the crystal chemistry of (high-valent) transition metal-stabilised cuprate superconductors. An examination of the chemistry of the mercurocuprate homologous series HgBa₂Ca_n−1Cu_nO_2n+2+δ leads us to propose that the inherent instability of the analogous strontium system (HgSr₂Ca_n−1Cu_nO_2n+2+δ) arises from bond-length mismatch at the interface between the rock-salt and perovskite layers. A simple set of principles can now be formalised for the stabilisation of strontium mercurocuprates via partial substitution of mercury by a high-valent transition metal within the crystal structure of interest. The chemistry of three different cuprate systems, in which high-valent transition metal ions adopt a pivotal role as structure-stabilising agents, are illustrated here. First, we demonstrate how a combination of structural stabilisation (by the substitution of rhenium onto the mercury site) combined with control of the copper oxidation state (via judicious control of the Nd³⁺:Ca²⁺ ratio), allows the successful synthesis of superconducting strontium analogues of HgBa₂CaCu₂O_6+δ in the (Hg_1−xRe_x)Sr₂(Nd_1−yCa_y)Cu₂O_6+δ system. Second, we report the successful preparation of superconducting Hg_1−xCr_xSr₂CuO_4+δ thin films, by laser ablation and ex situ mercuration. Finally, we describe a new family of layered cuprates with the general chemical formula (Cu_1−xTM_x)Sr₂(Y_1.2Ce_0.8)Cu₂O_10−δ, with TM=Ti, Cr, Mo, W, V and Re, in which these transition metal substituents, once again, fulfil a key role in structure stabilisation.     

Removal of heavy metal ions from aqueous solutions using carbon aerogel as an adsorbent

The removal of Cd(II), Pb(II), Hg(II), Cu(II), Ni(II), Mn(II) and Zn(II) by carbon aerogel has been found to be concentration, pH, contact time, adsorbent dose and temperature dependent. The adsorption parameters were determined using both Langmuir and Freundlich isotherm models. Surface complexation and ion exchange are the major removal mechanisms involved. The adsorption isotherm studies clearly indicated that the adsorptive behaviour of metal ions on carbon aerogel satisfies not only the Langmuir assumptions but also the Freundlich assumptions, i.e. multilayer formation on the surface of the adsorbent with an exponential distribution of site energy. The applicability of the Lagergren kinetic model has also been investigated. Thermodynamic constant (K(ad)), standard free energy (DeltaG(0)), enthalpy (DeltaH(0)) and entropy (DeltaS(0)) were calculated for predicting the nature of adsorption. The results indicate the potential application of this method for effluent treatment in industries and also provide strong evidence to support the adsorption mechanism proposed.     

Ion pairing as a strategy for extraction by modified supercritical carbon dioxide: extraction of radioactive metal ions

Supercritical fluid carbon dioxide was investigated for its potential to extract perrhenate ion pairs. This has implications for radioactive waste processing because Tc-99, the second row congener of Re, is produced in approximately 6% fission yield from nuclear fuel and pertechnetate is its most common chemical form in aqueous environments. The variables examined to maximize extraction of the perrhenate ion pair were temperature, pressure, solvent modification, and ion-pairing agents. The tetrabutyl-ammonium cation was found to form the most efficient ion pair for extracting perrhenate using methanol-modified (approximately 10%) SFCO2 at 70 degrees C and 477 atm, with 0.083 mg of Re/g of SFCO2 extracted.     

Rapid hard tooling by plasma spraying for injection molding and sheet metal forming

Amidst the harsh competition over the development of new products around the world, rapid prototyping, especially rapid tooling methods have received widespread attention. Amongst the rapid hard tooling methods, thermal spraying can manufacture metal molds without limitation of pattern size. However, it has the disadvantage that only soft metals with low melting points such as zinc alloy can be sprayed to original mold, such as a rapid prototyping model or a natural material pattern, due to their lack of heat resistance and shrinkage of spray metals. So the wear resistance of spray tool is poor, it can be used only for trial or small-lot production. In this study, attempts were made to improve the heat resistance by using composite materials made of ceramic and metal powders as the sprayed original mold materials, and using stainless steel, tungsten carbide alloy, iron–nickel–chromium alloy with excellent wear resistance as spraying materials, respectively. The results show that injection molding spray mold and sheet metal forming spray die can be made by transferring from natural patterns and rapid prototyping models. As the durability and dimensional accuracy of the sprayed tools has sharply improved, the tools can be used for mass production.     

检测金属离子的R-S-F结构型荧光分子传感器研究进展

Receptor-Spacer-Fluorophore(R-S-F)结构型荧光分子传感器是由可选择性结合客体的主体基团与传递信号的荧光团通过桥联基团连接而成的一类分子传感器,结合了超分子在分子识别中良好的选择性和荧光信号的高灵敏度两个优点,成为一类可用于检测金属离子并具巨大发展潜力的新型光学敏感材料.以超分子主体化合物...     

Porous CS monoliths and their adsorption ability for heavy metal ions

Highly porous chitosan (CS) monoliths were prepared by a unidirectional freeze-drying method and the adsorption performance of the monoliths for metal ions in aqueous solution was evaluated. The porous CS monoliths have excellent adsorption for a range of metal ions. The effect of the amount of porous CS monoliths, the pH, the adsorption time, the amount of the cross-linking agent, and the amount of disodium ethylenediamine tetraacetate (EDTA) on the saturated adsorption efficiency (Ade) were determined. The pH had the greatest influence on the adsorption behavior. Under optimal conditions (C(CU2?) = 800 mg/L, pH 6, and cross-linking agent = 0.15%) for the CS monoliths, the Ade for Cu(2+) exceeded 99%, and the saturated adsorption capacity (Q(s)) reached a value of 141.8 mg/g (2.23 mmol/g) in 4h. Moreover, the addition of EDTA can both increase the Q(s) and shorten the time that achieved the level. If EDTA was added, this level was achieved in 2h. The porous CS monoliths can be regenerated by soaking them in acid and their Ade is maintained.     

Polyrhodanine modified anodic aluminum oxide membrane for heavy metal ions removal

Polyrhodanine was immobilized onto the inner surface of anodic aluminum oxide (AAO) membrane via vapor deposition polymerization method. The polyrhodanine modified membrane was applied to remove heavy metal ions from aqueous solution because polyrhodanine could be coordinated with specific metal ions. Several parameters such as initial metal concentration, contact time and metal species were evaluated systematically for uptake efficiencies of the fabricated membrane under continuous flow condition. Adsorption isotherms of Hg(II) ion on the AAO-polyrhodanine membrane were analyzed with Langmuir and Freundlich isotherm models. The adsorption rate of Hg(II) ion on the membrane was obeyed by a pseudo-second order equation, indicating the chemical adsorption. The maximum removal capacity of Hg(II) ion onto the fabricated membrane was measured to be 4.2 mmol/g polymer. The AAO-polyrhodanine membrane had also remarkable uptake performance toward Ag(I) and Pb(II) ions. Furthermore, the polyrhodanine modified membrane could be recycled after recovery process. These results demonstrated that the polyrhodanine modified AAO membrane provided potential applications for removing the hazardous heavy metal ions from wastewater.     

Removal of heavy metal ions from water by using calcined phosphate as a new adsorbent

Calcined phosphate (CP) has been employed in our laboratories as a heterogeneous catalyst in a variety of reactions. In this study, CP was evaluated as a new product for removal of heavy metals from aqueous solution. Removal of Pb2+, Cu2+, and Zn2+ on the CP was investigated in batch experiments. The kinetic of lead on CP adsorption efficiency and adsorption process were evaluated and analysed using the theories of Langmuir and Freundlich. The influence of pH was studied. The adsorption capacity obtained at pH 5 were 85.6, 29.8, and 20.6 mg g(-1) for Pb2+, Cu2+ and Zn2+, respectively. We hypothesize at pH 2 and 3, the dissolution of CP and precipitation of a fluoropyromorphite for lead and the formation of solid-solution type fluorapatite for copper. The results obtained show that CP is a good adsorbent for these toxic heavy metals. The abundance of natural phosphate, its low price and non-aggressive nature towards the environment are advantage for its utilisation in point of view of wastewater and wastes clean up.