Ying Xiong

Selective recovery of precious metals by persimmon waste chemically modified with dimethylamine.

Persimmon waste was chemically modified with dimethylamine (DMA) to obtain a tertiary-amine-type gel, named DMA persimmon waste gel (DMA-PW). It was found to be effective for the adsorption of Au(III), Pd(II), and Pt(IV) in hydrochloric acid medium. In contrast, base metals such as Cu(II), Zn(II), Fe(III), and Ni(II) were not practically adsorbed. The formation of ion pairs of the metal chloro complex anions with the protonated adsorption gels was proposed as the main adsorption process. The gel exhibited selectivity only for precious metals with a remarkably high capacity for Au(III), i.e., 5.63 mol/kg dry gel and comparable capacities, i.e., 0.42 and 0.28 mol/kg for Pd(II) and Pt(IV), respectively. According to the kinetic and electrochemical studies, the adsorption rate of Au(III) was greatly enhanced by the chemical modification. Also, its excellent adsorption characteristics for the precious metals were confirmed by adsorption and elution tests using a column packed with the DMA-PW gel.

Selective adsorption of molybdenum(VI) from Mo-Re bearing effluent by chemically modified astringent persimmon.

Astringent persimmon was chemically cross-linked by formaldehyde to obtain a novel kind of adsorption gel, which was named as APF gel. The adsorption behaviors of Mo(VI) and Re(VII) along with other coexisting metals onto the APF gel were studied in the present paper. The APF gel was found to be effective for the adsorption of Mo(VI) while the gel is almost completely inert toward rhenium and calcium over the whole hydrochloric acid concentration region. The APF gel has a low affinity for iron, copper, lead, nickel, manganese and zinc ions when the concentration of HCl is higher than 1 mol/L. The gel exhibited selectivity only for Mo(VI) with a remarkably high adsorption capacity 1.05 mol/kg, and the adsorption behavior obeys the Langmuir model. According to the thermodynamic and kinetic studies, the endothermic adsorption process followed pseudo-second order kinetics. Also, its excellent adsorption characteristics for Mo(VI) were confirmed by the adsorption and elution tests using a column packed with the APF gel. The result provides a new approach for the recovery of Mo(VI) from a industrial waste effluent.

Contribution of tertiary amino groups to Re(VII) biosorption on modified corn stalk: competitiveness and regularity.

The effects of basic strength and steric hindrance of gels modified by dimethylamine, diethylamine, di-n-octylamine and di-2-ethylhexylamine, respectively, on rhenium (Re(VII)) adsorption capacity and selectivity were discussed. By comparing with the adsorption of other coexisting metals, such as Mo(VI), Cu(II), Pb(II), Fe(III), Zn(II), Mn(VII) and Ni(II), the gel modified by di-n-octylamine (DNOA-OCS) showed a high affinity for Re(VII) at higher hydrochloric acid concentration (C(H)(+)≥1.0 mol L(-1)), and the maximum adsorption capacity was 98.69 mg g(-1). This article not only described the adsorption behavior but also suggested isotherms, kinetics and thermodynamics of Re(VII) onto the DNOA-OCS gel in an aqueous medium using several models. Further study on adsorption of rhenium in a fixed-bed column packed with the DNOA-OCS gel under continuous and recirculating modes could confirm that the corn stalk gel modified by di-n-octylamine could be used as the adsorbent of Re(VII) from Mo-containing wastewater.

A new approach for rhenium(VII) recovery by using modified brown algae Laminaria japonica adsorbent

Brown algae Laminaria japonica was chemically modified with sulfuric acid to obtain a crosslinked brown algae gel (CAS). The CAS gel showed a high affinity for Re(VII) comparing with other biomass gels, and the maximum adsorption capacity was evaluated as 37.20 mg g(-1) in case of pH 6, which could be explained by their different adsorption mechanisms. The adsorption equilibrium, kinetics and thermodynamic study for Re(VII) on the CAS gel was discussed in detail by the several models, such as Langmuir, Freundlich, Temkin and Dubinin-Radushkevich model for kinetics analysis, the pseudo first, the second-order, the Elovich and intraparticle diffusion equation for equilibrium analysis. Reutilization of the CAS gel was confirmed up to three adsorption-elution cycles in column-mode operation with no damage of gel, packed in the column. The result also provides a new approach for the recovery of Re(VII) from Re-containing wastewater by using the modified brown algae gel.

Investigation on the removal of Mo(VI) from Mo-Re containing wastewater by chemically modified persimmon residua.

Persimmon waste was chemically modified by crosslinking with concentrated sulfuric acid to obtain a novel kind of adsorption gel, which was termed as crosslinked persimmon tannin (CPT), hereinafter. The adsorption behaviors of Mo(VI) with other coexisting metal ions onto the CPT gel were investigated. The gel exhibited selectivity only for Mo(VI) ions evidenced by the high value of separation factor of molybdenum and rhenium (β(Mo/Re)=164.37), and the adsorption mechanism of Mo(VI) as a multispecies was studied. The molybdenum adsorption behavior conforms to the Langmuir model with a remarkably high adsorption capacity of 0.56 mol/kg. A kinetic study for the adsorption of molybdenum at various temperatures confirmed that the endothermic adsorption process followed pseudo-second order kinetics. Moreover, its excellent adsorption properties and applicability for Mo(VI) were demonstrated by the removal and separation of Mo(VI) from different Mo-Re containing industrial wastewaters.

Selective recovery of Ag(I) coordination anion from simulate nickel electrolyte using corn stalk based adsorbent modified by ammonia–thiosemicarbazide

In nickel electrolyte, Ag(I) was present at trace level concentration (10-20 mg L(-1)) and existed in the form of AgCli(1-i) coordination anion, instead of Ag(+) positive ion usually in several sources. In the present study, TSC-NH3-OCS adsorbent based on natural corn stalk modified by ammonia (NH3)-thiosemicarbazide (TSC) was synthesized and characterized using some instrumental techniques. The TSC-NH3-OCS adsorbent could selectively adsorb Ag(I) as AgCl(i)(1-i) coordination anion from the Ag(I)-Cu(II)-Ni(II) simulate nickel electrolyte, especially in the case of the very high levels of Cu(II) and Ni(II), which significantly outperforms the commercial available resins. The adsorption mechanism was believed to be electrostatic interaction of the protonated bands of AgCl4(3-) with protonated thiol form of the thioamide units by FTIR and XPS analysis. The maximum adsorption capacity in the Ag(I) single and Ag(I)-Cu(II)-Ni(II) ternary system were obtained and calculated as 153.54 and 46.69 mg g(-1), respectively. The reasons that the maximum adsorption capacity of AgCl(i)(1-i) from the single and ternary system varied widely could be explained by adsorption kinetic and thermodynamic results. In addition, three successive sorption/desorption cycle runs from ternary system were performed which indicated that the TSC-NH3-OCS adsorbent has a good performance for recovery Ag(I) from simulate nickel electrolyte.

Physicochemical properties of air and water stable rhenium ionic liquids.

Air and water stable ionic liquids (ILs) based on catalytic functional metal rhenium, [C(n)mim][ReO(4)](n = 2,4,5,6)(1-alkyl-3-methylimidazolium perrhenate), are designed and synthesized. Their density and surface tension are measured in the temperature range of 293.15-343.15 ± 0.05 K. Some physical-chemical properties of the ILs have been calculated or estimated by the empirical methods. The ion parachor is put forward and calculated by two extrathermodynamic assumptions. According to the interstice model, the thermal expansion coefficient of ILs [C(n)mim][ReO(4)], α, are calculated and in comparison with experimental values, their magnitude order is in good agreement.

Kinetics and mechanism of Re(VII) extraction and separation from Mo(VI) with trialkyl amine

Abstract The extraction kinetics of rhenium(VII) or molybdenum(VI) with trialkyl amine (N235, R 3 N, R=C 8 –C 10 ) dissolved in heptane were investigated by constant interfacial cell with laminar flow, which aimed to identify the extraction regime, reaction zone and rate equations. The influence of stirring speed, temperature, specific interfacial area, extraction concentration and chlorine concentration on the extraction of both metals was studied. It is concluded that the extractions of Re(VII) and Mo(VI) both take place at the liquid–liquid interface, while the extraction regimes are chemically-controlled for rhenium and mixed controlled for molybdenum, respectively. The extraction rate equations and the rate-determining step were obtained under the experimental conditions, and the extraction rate constant of Re(VII) or Mo(VI) with N235 was calculated. These obtained kinetics parameters are different between Re(VII) and Mo(VI), which provides better possibilities for Re(VII) and Mo(VI) separations at proper conditions.

Aminopropyl-grafted various silica mesostructures for adsorption of molybdenum ions from Re-containing effluent

Four different silica mesostructures, SBA-15 with mesopore size (8.5xa0nm), SBA-15 with mesopore size (10.3xa0nm), mesocellular foam (MCF) with uniform cell size (33.2xa0nm), and MCF with bimodal mesoporosity, were grafted with aminopropyl groups and used for selective recovery of Mo(VI) from Re(VII)-containing effluent. Adsorption isotherms and mechanism of Mo(VI) adsorption on these materials were studied. The adsorbed complexes of Mo(VI) could be formed by ion exchange process or/and by chelation reaction. This study shows a new approach for fractional recovery and separation of Mo(VI) from Re(VII) by using amino-modified SBA-15-type mesoporous silica.

Selective Adsorption of Mo(VI) From Re(VII) Containing Effluent on Orange Waste Gel Modified by Ethylenediamine, Diethylamine, and Triethylamine

New adsorption gels were prepared by chemically immobilizing functional groups of ethylenediamine, diethylamine and/or triethylamine on orange waste, named OW-en, OW-DEA, and OW-TEA, respectively. By comparing with the adsorption of other coexisting metals, such as Re(VII), Pb(II), Fe(III), Zn(II), Mn(VII), Ca(II), and Cu(II), the novel gels exhibited selectivity only for Mo(VI) and the adsorption behavior obeys the Langmuir model. The maximum adsorption capacity for molybdenum was in the order, OW-en (2.17 mol/kg) > OW-TEA (1.26 mol/kg) > OW-DEA (0.88 mol/kg). A kinetic study for the adsorption of molybdenum at various temperatures confirmed that the endothermic adsorption process followed pseudo-second order kinetics. In addition, its excellent adsorption characteristics for Mo(VI) were confirmed by the adsorption and elution tests using a column packed with the OW-en gel, especially by separation of Mo(VI) from Mo-Re containing industrial effluent.