The values of GΘ,EΘ or pH from 110 to 160℃ were calculated and the relevant potential expressions were obtained.E-pH diagrams of ZnS-H2O system at oxygen partial pressure of 0.8 MPa,ionic activity of 1.0 and differ...The values of GΘ,EΘ or pH from 110 to 160℃ were calculated and the relevant potential expressions were obtained.E-pH diagrams of ZnS-H2O system at oxygen partial pressure of 0.8 MPa,ionic activity of 1.0 and different temperatures were drawn through thermodynamical calculation.With the temperature increasing,the stable regions of S and Zn(Ⅱ) in the E-pH diagrams become gradually larger,but the amplification decreases over 150℃.The impacts of leaching parameters,such as temperature,liquid to solid ratio,initial acidic concentration,leaching time,oxygen partial pressure and stirring speed on the leaching rate of Zn(Ⅱ) and conversion rate of S in the single factor of high pressure leaching experiment of ZnS in autoclave,were studied.The leaching residue was examined by X-ray fluorescence(XRF) chemical composition identification and X-ray diffraction(XRD) phase identification,and the content of the leaching solution was tested by inductively coupled plasma-atomic emission spectrometry(ICP).The experimental results indicate that the leaching rate of zinc increases from 60.05% to 97.85% and the conversion rate of sulfur increases from 38.90% to 80.92% with the temperature increasing from 110℃ to 150℃,5:1 of liquid-to-solid ratio,150 g/L of initial acidic concentration,120 min of leaching time,0.8 MPa of oxygen partial pressure,and 480 r/min of stirring speed,which tend to be stable over 150℃.The experimental results correspond with theoretical calculation.展开更多
Heavy metal determination was carried out by applying the solid phase extraction （SPE） method in batch mode followed by atomic absorption spectroscopy （AAS） and inductively coupled plasma atomic emission spectrosc...Heavy metal determination was carried out by applying the solid phase extraction （SPE） method in batch mode followed by atomic absorption spectroscopy （AAS） and inductively coupled plasma atomic emission spectrosco py （ICP-AES） from aqueous solutions using Ghezeljeh montmorillonite nanoclay as a new natural adsorbent. The Ghezeljeh clay is characterized by using Fourier Transform Infrared （FT-IR） Spectroscopy, Scanning Electron Mi- croscopy-Energy Dispersive Spectrometry （SEM-EDS） and X-ray Diffractometry （XRD） and X-ray Fluorescence （XRF）. The results of XRD and FT-IR of nanoclay confirm that montmorillonite is the dominant mineral phase. Based on SEM images of Ghezeljeh clay, it can be seen that the distance between the plates is Nano. The effects of varying parameters such as initial concentration of metal ions, pH and type of buffer solutions, amount of ad- sorbent, contact time, and temperature on the adsorption process were examined. The effect of various interfer- ing ions was studied. The adsorption data correlated with Freundlich, Langmuir, Dubinin-Radushkevich （D-R）, and Temkin isotherms. The Langmuir and Freundlich isotherms showed the best fit to the equilibrium data for Hg（II）, but the equilibrium nature of Cu（ll） adsorption has been described by the Langmuir isotherm. The kinetic data were described with pseudo-first-order, pseudo-second-order and double-exponential models, The adsorp- tion process follows a pseudo-second-order reaction scheme, Calculation of AGσ, △Hσ and ASσ showed that tilenature of Hg（II） ion sorption onto the Ghezeljeh nanoclay was endothermic and was favored at higher temper- attire, and the nature of Cu（II） ion sorption was exothermic and was favored at lower temperature,展开更多
A method to determine Fe（Ⅲ） by thin layer resin phase spectrophotometry has been developed in this paper. The colored complex formed by Fe（Ⅲ） and 1,2-benzendiol is concentrated on the 717^# resin, then Fe（Ⅲ） ...A method to determine Fe（Ⅲ） by thin layer resin phase spectrophotometry has been developed in this paper. The colored complex formed by Fe（Ⅲ） and 1,2-benzendiol is concentrated on the 717^# resin, then Fe（Ⅲ） can be determined directly by making thin layer. The method is sensitive with a apparent molar absorption of 4.8×10^4L/mol.cm, which is 16 times higher than that of liquid phase spectrophotornetry, most coexisting ions do not influence the determination. The detection limit for Fe（Ⅲ） is 1.47μg/L with the precision of 3.3% [n=6, 7μg/50mL Fe（Ⅲ）]. The calibration curve is linear in the range of 0-25μg/50mL. The preposed method was applied to the determination of Fe（Ⅲ） in water sample with satisfactory results.展开更多
基金Project (2007CB613504) supported by the National Basic Research Program of ChinaProject(20050145029) supported by the PhD Programs Foundation of Ministry of Education of ChinaProject(2005221012) supported by the Science and Technology Talents Fund for Excellent Youth of Liaoning Province, China
文摘The values of GΘ,EΘ or pH from 110 to 160℃ were calculated and the relevant potential expressions were obtained.E-pH diagrams of ZnS-H2O system at oxygen partial pressure of 0.8 MPa,ionic activity of 1.0 and different temperatures were drawn through thermodynamical calculation.With the temperature increasing,the stable regions of S and Zn(Ⅱ) in the E-pH diagrams become gradually larger,but the amplification decreases over 150℃.The impacts of leaching parameters,such as temperature,liquid to solid ratio,initial acidic concentration,leaching time,oxygen partial pressure and stirring speed on the leaching rate of Zn(Ⅱ) and conversion rate of S in the single factor of high pressure leaching experiment of ZnS in autoclave,were studied.The leaching residue was examined by X-ray fluorescence(XRF) chemical composition identification and X-ray diffraction(XRD) phase identification,and the content of the leaching solution was tested by inductively coupled plasma-atomic emission spectrometry(ICP).The experimental results indicate that the leaching rate of zinc increases from 60.05% to 97.85% and the conversion rate of sulfur increases from 38.90% to 80.92% with the temperature increasing from 110℃ to 150℃,5:1 of liquid-to-solid ratio,150 g/L of initial acidic concentration,120 min of leaching time,0.8 MPa of oxygen partial pressure,and 480 r/min of stirring speed,which tend to be stable over 150℃.The experimental results correspond with theoretical calculation.
基金financial support for this work by the Imam Khomeini International University (IKIU)Mines and Mining Industries Development and Renovation Organization of Iran (IMIDRO)
文摘Heavy metal determination was carried out by applying the solid phase extraction （SPE） method in batch mode followed by atomic absorption spectroscopy （AAS） and inductively coupled plasma atomic emission spectrosco py （ICP-AES） from aqueous solutions using Ghezeljeh montmorillonite nanoclay as a new natural adsorbent. The Ghezeljeh clay is characterized by using Fourier Transform Infrared （FT-IR） Spectroscopy, Scanning Electron Mi- croscopy-Energy Dispersive Spectrometry （SEM-EDS） and X-ray Diffractometry （XRD） and X-ray Fluorescence （XRF）. The results of XRD and FT-IR of nanoclay confirm that montmorillonite is the dominant mineral phase. Based on SEM images of Ghezeljeh clay, it can be seen that the distance between the plates is Nano. The effects of varying parameters such as initial concentration of metal ions, pH and type of buffer solutions, amount of ad- sorbent, contact time, and temperature on the adsorption process were examined. The effect of various interfer- ing ions was studied. The adsorption data correlated with Freundlich, Langmuir, Dubinin-Radushkevich （D-R）, and Temkin isotherms. The Langmuir and Freundlich isotherms showed the best fit to the equilibrium data for Hg（II）, but the equilibrium nature of Cu（ll） adsorption has been described by the Langmuir isotherm. The kinetic data were described with pseudo-first-order, pseudo-second-order and double-exponential models, The adsorp- tion process follows a pseudo-second-order reaction scheme, Calculation of AGσ, △Hσ and ASσ showed that tilenature of Hg（II） ion sorption onto the Ghezeljeh nanoclay was endothermic and was favored at higher temper- attire, and the nature of Cu（II） ion sorption was exothermic and was favored at lower temperature,
基金Advanced Fund Item of Jiangsu University (07KJB610021)
文摘A method to determine Fe（Ⅲ） by thin layer resin phase spectrophotometry has been developed in this paper. The colored complex formed by Fe（Ⅲ） and 1,2-benzendiol is concentrated on the 717^# resin, then Fe（Ⅲ） can be determined directly by making thin layer. The method is sensitive with a apparent molar absorption of 4.8×10^4L/mol.cm, which is 16 times higher than that of liquid phase spectrophotornetry, most coexisting ions do not influence the determination. The detection limit for Fe（Ⅲ） is 1.47μg/L with the precision of 3.3% [n=6, 7μg/50mL Fe（Ⅲ）]. The calibration curve is linear in the range of 0-25μg/50mL. The preposed method was applied to the determination of Fe（Ⅲ） in water sample with satisfactory results.
