Xanthates are organic synthesized substances with a potentially wide range of applications. They may serve as essential components of many compounds or materials that also play a vital role in various industrial and s...Xanthates are organic synthesized substances with a potentially wide range of applications. They may serve as essential components of many compounds or materials that also play a vital role in various industrial and socio-economic processes. Addressing the question of the use of xanthates without considering their toxicity, and their decomposition process and products would be ecologically and healthily less sustainable. To date, related information is still dispersed and less known to the public. Therefore, this work provides a comprehensive overview of the existing information on the essentiality, fate, ecotoxicity, and health effects of xanthates and associated compounds. According to available information from scientific, technical, and professional circles, xanthates are diverse, usually with a carbon chain of two to six carbon atoms. They play a crucial role in the sectors of the mining and mineral processing industry, agriculture, wastewater treatment, metal protection, rubber vulcanization, the pharmaceutical industry, and medicine. Xanthates’ degradation under different factors and mechanisms, which determine their fate in the environment, leads to the formation of toxic substances, mainly carbon disulfide, carbonyl sulfide, hydrogen sulfide, and hydrogen peroxide. Xanthates and xanthates degradation products are seriously hazardous to humans, animals, soil and aquatic organisms, enzymatic system, etc. Simultaneous exposure to xanthates and metals results in the magnification or reduction of their toxicity level, depending on the exposed organisms. Such toxicological dimensions should attract more scientific and public attention for more safe production, use, storage, and disposal of xanthates. Due to the high affinity of xanthates for metal, xanthates-modified compounds are efficient metal chelating agents. Such a property should be explored to develop potentially low-cost and effective alternatives for metal removal and recovery from contaminated media. The same applies to developing appropriate methods for the evaluation and management of the simultaneous presence of xanthates and metals in the environment.展开更多
The flotation of hemimorphite using the S(Ⅱ)–Pb(Ⅱ)–xanthate process,which includes sulfidization with sodium sulfide,activation by lead cations,and subsequent flotation with xanthate,was investigated.The flotation...The flotation of hemimorphite using the S(Ⅱ)–Pb(Ⅱ)–xanthate process,which includes sulfidization with sodium sulfide,activation by lead cations,and subsequent flotation with xanthate,was investigated.The flotation results indicated that hemimorphite floats when the S(Ⅱ)–Pb(Ⅱ)–xanthate process is used; a maximum recovery of approximately 90% was obtained.Zeta-potential,contact-angle,scanning electron microscopy–energy-dispersive spectrometry(SEM–EDS),and diffuse-reflectance infrared Fourier transform spectroscopy(DRIFTS) measurements were used to characterize the activation products on the hemimorphite surface and their subsequent interaction with sodium butyl xanthate(SBX).The results showed that a Zn S coating formed on the hemimorphite surface after the sample was conditioned in an Na2 S solution.However,the formation of a Zn S coating on the hemimorphite surface did not improve hemimorphite flotation.With the subsequent addition of lead cations,Pb S species formed on the mineral surface.The formation of the Pb S species on the surface of hemimorphite significantly increased the adsorption capacity of SBX,forming lead xanthate(referred to as chemical adsorption) and leading to a substantial improvement in hemimorphite flotation.Our results indicate that the addition of lead cations is a critical step in the successful flotation of hemimorphite using the sulfidization–lead ion activation–xanthate process.展开更多
Preparation of orange peel xanthate and its adsorption behaviors of five heavy metals(Cu 2+ ,Cd 2+ ,Pb 2+ ,Zn 2+ and Ni 2+ ) were studied.FTIR spectra,Zeta potentials and TG analysis were used to characterize prepared...Preparation of orange peel xanthate and its adsorption behaviors of five heavy metals(Cu 2+ ,Cd 2+ ,Pb 2+ ,Zn 2+ and Ni 2+ ) were studied.FTIR spectra,Zeta potentials and TG analysis were used to characterize prepared orange peel xanthate.Effects of various parameters including equilibrium pH,initial metal ion concentration and adsorption time on the adsorption processes for the five metal ions were investigated.It was found that for all five metal ions,the adsorption isotherms agreed Langmuir model very well and the maximum adsorption capacities of Cu2 +,Cd 2+,Pb 2+,Zn 2+and Ni 2+were obtained as 77.60,76.57,218.34,49.85 and 15.45 mg/g,respectively.All adsorption processes can attain equilibrium within 20 min and kinetics was well fitted by psesudo-second order equation.It is proposed that the adsorption mechanism was complexation.展开更多
Wolframite notation with benzyl arsonic acid and sodium butyl xanthate is studied,at first.It shows the efficiency of mineral processig is good when the two agents are added together.Then the synergism of sodium butyl...Wolframite notation with benzyl arsonic acid and sodium butyl xanthate is studied,at first.It shows the efficiency of mineral processig is good when the two agents are added together.Then the synergism of sodium butyl xanthate and benzyl arsonic acid is studied also by HPLC.展开更多
A subbituminous coal was oxidized with air at 150℃on a fixed bed for 4 h and xanthated with carbondisulfide in a basic solution,at 30 or 5-10℃.This xanthated coal was evaluated for the removal of Hg^(2+)and Cd^(2+)f...A subbituminous coal was oxidized with air at 150℃on a fixed bed for 4 h and xanthated with carbondisulfide in a basic solution,at 30 or 5-10℃.This xanthated coal was evaluated for the removal of Hg^(2+)and Cd^(2+)from 7,000 mg/L aqueous solutions;metal concentrations were detemmined by atomic absorption spectrometry.The ionexchange of the xanthated coal was compared against those of the original subbituminous coal,a sulfonated subbituminouscoal,activated carbon,commercial activated carbon,and commercial synthetic resin.The commercial synthetic resinshowed the highest exchange capacity(concentration factor 98%)followed by the xanthated coal(concentration factor 96%).The retention of cadmium on the sulfonated subbituminous coal was lower(exchange capacity 0.56 meq/g)thanthat of xanthated coals(1.85±0.09 meq/g).Our xanthated coal showed a better Cd^(2+)removal(8l%o against 15%)than anon preoxidized 40-h-xanthated coal,which shows that oxidation of coal increased the amount of oxygenated groups whichenhanced xanthation.展开更多
Three HPLC methods for the separation and determination of xanthate mixtures are described.The chromatographic behaviours,advantages and application ranges of various:methods have been discussed in detail.A calculatio...Three HPLC methods for the separation and determination of xanthate mixtures are described.The chromatographic behaviours,advantages and application ranges of various:methods have been discussed in detail.A calculation method for determining the results of individual xanthates from the complicated chromatographic peaks of xanthate mixtures is presented.The limits of detection are 0.15-2.0ng.展开更多
Cobalt isopropyl xanthate thin films (CXTFs) were deposited via chemical bath deposition onto different substrates:commercial glass (CG), indium tin oxide (ITO), and poly(methyl methacrylate) (PMM). Isoprop...Cobalt isopropyl xanthate thin films (CXTFs) were deposited via chemical bath deposition onto different substrates:commercial glass (CG), indium tin oxide (ITO), and poly(methyl methacrylate) (PMM). Isopropyl xanthate was synthesized according to a method described in the literature. The cobalt nitrate and isopropyl xanthate were mixed in a beaker, which allowed the thin films to be deposited via a simple ion-ion mechanism. The transmission, reflectivity, refractive index, dielectric constant, and optical conductivity were investigated for various thin films coated onto different substrates. An ultraviolet-visible spectrophotometer was used to measure the optical properties of the thin films. The lowest value of the transmission and the highest value of the refractive index were observed for the thin films deposited onto PMM. The structure of the cobalt xanthate was characterized by Fourier transform infrared (FTIR) spectroscopy, which was measured using a Perkin-Elmer Spectrum 400 spectrometer. The stretching vibration of the Co-S bonds was observed at 359 cm^-1 in the FTIR spectrum of the CXTFs.展开更多
A simple and fast ultraviolet spectrophotometric method was used to determineselenium (Ⅳ) through the formation, separaion and quantitative determination of potassium butylxanthae -selenium complex. The complex ab...A simple and fast ultraviolet spectrophotometric method was used to determineselenium (Ⅳ) through the formation, separaion and quantitative determination of potassium butylxanthae -selenium complex. The complex absorbed light sharply at 375 nm. The optimum acidity ofthe complex formation was between pH 3.4 - 4.0. The absorption value was no change in 120 minutesafter the comlex was extracted by Carbon tetraChioride. The sensitivity of the colour reation was 0.2ng cm-2, The content of selenimp (Ⅳ) was within 0-30 μg and linear rclation was good,Y=0.07X+0.025, relevent coefficient r=0.9997. A great quantity of I, Cu, Co, the and SO4-2, PO4-3contained in .the Sample had no effect on the results ofdetenninion when seldsum was determined.When content of Fe was over l00gμg/ml and Zn was over 180μg/ml, there was diotance to the determination, but the disturbance was rem0ved by adding EDTA. When making use of the method todetermine containin seldsum additivef Cv =6.85, rate of recovery was 97.2%, wild jujubef;Cv=3.22,rate of recovery was 90. 1%, soil Samlef Cv=4.64, rate of recovery was 86.2%. The method for sensitivity measured was apprtoate to 2, 3-diamino naphthalene (DAN) fluorescence method.展开更多
Fifteen M(S2COR)n complexes were prepared.According to the data provided by IR,UV-Vis absorption spectrometry and X-ray diffraction,this paper covers the relationship between molecular structures of xanthate complexes...Fifteen M(S2COR)n complexes were prepared.According to the data provided by IR,UV-Vis absorption spectrometry and X-ray diffraction,this paper covers the relationship between molecular structures of xanthate complexes and their absorption spectra and a criterion of chelate stability is also proposed.The stability mechanism of xanthate chelates and related rules were investigated.展开更多
This review discusses the numerous routes to all-carbon quaternary centers based on the unique radical chemistry of xanthates. Itsummarizes the various approaches to the synthesis of tertiary xanthates then describes ...This review discusses the numerous routes to all-carbon quaternary centers based on the unique radical chemistry of xanthates. Itsummarizes the various approaches to the synthesis of tertiary xanthates then describes the intra- and intermolecular radicaladditions and combinations thereof that have so far been used to construct quaternary centers.展开更多
Xanthated crosslinked chitosan(XCCS) resin prepared under microwave irradiation were used for adsorbing Au(Ⅲ) ions in hydrochloric acid medium.The influence of pH and temperature on the adsorption capacity of XCCS wa...Xanthated crosslinked chitosan(XCCS) resin prepared under microwave irradiation were used for adsorbing Au(Ⅲ) ions in hydrochloric acid medium.The influence of pH and temperature on the adsorption capacity of XCCS was investigated.The original XCCS and the loaded XCCS were characterized by scanning electron microscope(SEM) and X-ray diffraction(XRD),respectively.The results indicate that the XCCS has ability to adsorb Au(Ⅲ) ions and the maximum adsorption capacity of Au(Ⅲ) ions on XCCS is observed at pH 1 and 20℃.The data of batch adsorption tests are fitted to kinetic models and isotherm models,respectively.The kinetics of adsorption process is found to follow pseudo-second-order kinetic rate model,and equilibrium data agree very well with the Langmuir model.Thermodynamic calculation of the Au(Ⅲ) ions adsorption process indicates that the adsorption process is spontaneous and endothermic.展开更多
Nano-drug delivery systems with multiple stimulus-responsive capabilities have superior response performance and efficient drug release.Nevertheless,it is sophisticated to construct multiple stimulus-responsive system...Nano-drug delivery systems with multiple stimulus-responsive capabilities have superior response performance and efficient drug release.Nevertheless,it is sophisticated to construct multiple stimulus-responsive systems where the two or more functional groups need to be introduced simultaneously.Xanthate,one functional group with pH and H2O2 stimulus responsiveness,has significant potential applications for building dual-responsive drug delivery system.Herein,we present a novel dual stimuli-responsive supramolecular drug delivery system by using sodium xanthate derivative(SXD)as guest molecule and quaternary ammonium capped pillar[5]arene(QAP5)as host molecule through host-guest interaction on the basis of electrostatic interaction.The amphiphile QAP5⊃SXD could self-assemble into vesicles to efficiently load the anti-cancer drug DOX.The experimental results showed that QAP5⊃SXD nanoparticles could achieve efficient drug delivery and controlled release in the tumor microenvironment.Cytotoxicity experiments proved that DOX@QAP5⊃SXD nanoparticles could significantly improve the anticancer efficiency of free DOX on cancer cells.The present study provides an efficient strategy to develop supramolecular nanocarriers with dual-responsiveness in one functional group for controlled drug release.展开更多
The adsorption behavior of butyl xanthate on the surface of lead oxide was investigated using continuous online in situ attenuated total reflectance Fourier transform infrared(ATR-FTIR) spectroscopy technique and tw...The adsorption behavior of butyl xanthate on the surface of lead oxide was investigated using continuous online in situ attenuated total reflectance Fourier transform infrared(ATR-FTIR) spectroscopy technique and two dimensional(2D) correlation analysis.The adsorbed layer studied was prepared by coating α-PbO particles onto the surfaces of the ZnSe crystal.The appearance of spectral peaks at 1203 cm^-1,1033 cm^-1 and their red shift indicated the formation and aggregation of xanthate at the surface of α-PbO.According to 1R intensity changes after rinsing with deionized water and a NaOH solution,the adsorption was proved to be a chemisorption type.The competition between xanthate and OH^- for the surfaces leads to desorption of xanthate at higher pH.The technique of 2D correlation ATR-FTIR spectroscopy was used to evaluate the changing order of spectral intensities in the adsorption process,and the results indicated that xanthate micelles were formed at the surfaces.The adsorption kinetics of butyl xanthate was found to be a pseudo-second-order reaction model and the adsorption capacity of butyl xanthate at α-PbO was as high as 281 mg g^-1 after 150 min.展开更多
A new ruthenium complex containing bidentate xanthate ligands was synthesized in a good yield. This complex was characterized by elemental analysis, proton nuclear magnetic resonance(tH NMR), Fourier transform infra...A new ruthenium complex containing bidentate xanthate ligands was synthesized in a good yield. This complex was characterized by elemental analysis, proton nuclear magnetic resonance(tH NMR), Fourier transform infrared(FTIR) and UV-Vis spectroscopies. The cyclic voltammetry of the complex revealed one quasi-redox wave centered at Ru(III)/Ru(II) couple, indicating its catalytic potential. So the preparation of a glass carbon electrode modified with ruthenium xanthate complex and its electrocatalytic activity toward the oxidation of tryptophan(Trp) were also studied. The experimental results show that the modified electrode had excellent electrocatalytic activity for the oxidation of tryptophan. Moreover, under the optimized conditions, the oxidation peak current was propor- tional to tryptophan concentration in a range of 2.5×10-7 to 5.0× 10-5 mol/L with a correlation coefficient of 0.9928 and a detection limit of 8.3 × 10-8 mol/L(S/N=3). Using the proposed method, tryptophan was successfully determined in pharmaceutical samples with standard addition method.展开更多
Enargite is typically associated with chalcocite.Owing to the similarity in the flotation behaviors of these minerals,both minerals are reported to concentrate in the conventional flotation circuit.However,inorganic a...Enargite is typically associated with chalcocite.Owing to the similarity in the flotation behaviors of these minerals,both minerals are reported to concentrate in the conventional flotation circuit.However,inorganic arsenic in enargite can decrease the copper concentrate quality and increase the operating cost of processing this concentrate.Separating these minerals is important for cleaner copper production to avoid these effects.In this context,this study investigated the effect of hydrogen peroxide(H_(2)O_(2))treatment on the flotation behavior of chalcocite and enargite.Flotation tests of pure and mixed minerals indicated that H_(2)O_(2)treatment reduced the floatability of chalcocite and enargite by forming sulfate and copper hydroxide on their surfaces.Despite the detrimental effect of the H_(2)O_(2)treatment,there was a narrow window of H_(2)O_(2)concentration for separating both minerals,in which enargite floated and chalcocite was depressed.This selective flotation behavior was caused by the rapid adsorption of potassium amyl xanthate(KAX)and lower surface oxidation of enargite compared with that of chalcocite.展开更多
The direct sulfidization of cuprite is inefficient because cuprite is a copper-oxide mineral with a strong surface hydrophilicity.In this study,oxidant was used to modify cuprite surfaces to regulate the sulfidization...The direct sulfidization of cuprite is inefficient because cuprite is a copper-oxide mineral with a strong surface hydrophilicity.In this study,oxidant was used to modify cuprite surfaces to regulate the sulfidization of cuprite.Microflotation tests showed that the flotation recovery of pre-oxidized cuprite was nearly25% higher than that of direct sulfidization flotation,which indicates that the cuprite surface activity was enhanced after pre-oxidation by Cu(Ⅰ) species(weak affinity with sulfur ions) transformation to Cu(Ⅱ)species(strong affinity with sulfur ions).Zeta potential,scanning electron microscopy-energy dispersive X-ray spectroscopy,X-ray photoelectron spectroscopy,and time-of-flight secondary ion mass spectrometry results showed that pre-oxidation improved cuprite sulfidization and promoted the formation of copper-sulfide species on the cuprite surfaces.The mineral surface stability and thus,xanthate species adsorption on the cuprite surfaces were improved.The surface-adsorption measurements and infrared spectroscopy showed that a large amount of xanthate species was adsorbed onto the sulfidized cuprite surfaces after pre-oxidation,which enhanced the cuprite hydrophobicity and improved the cuprite flotation.展开更多
Comparative voltammetry and differential double-layer capacitance studies were performed to evaluate interfacial interactions between cnalcopyrite(CuFeS2) and n-isopropyl xanthate(X) in the presence of ammonium bi...Comparative voltammetry and differential double-layer capacitance studies were performed to evaluate interfacial interactions between cnalcopyrite(CuFeS2) and n-isopropyl xanthate(X) in the presence of ammonium bisulfite/39wt%SO2 and caustic starch at different pH values.Raman spectroscopy,Fourier transform infrared(FTIR) spectroscopy,contact angle measurements,and microflotation tests were used to establish the type and extent of xanthate adsorption as well as the species involved under different mineral surface conditions in this study.The results demonstrate that the species that favor a greater hydrophobicity of chalcopyrite are primarily CuX and S^0,whereas oxides and hydroxides of Cu and Fe as well as an excess of starch decrease the hydrophobicity.A conditioning of the mineral surface with ammonium bisulfite/39wt%SO2 at pH 6 promotes the activation of surface and enhances the xanthate adsorption.However,this effect is diminished at pH ≥ 8,when an excess of starch is added during the preconditioning step.展开更多
The surface species transformation of oxidized carrollite processing with NaHS and KBX was investigated.Flotation and contact angle tests indicate that the combination of NaHS and KBX takes a better flotation performa...The surface species transformation of oxidized carrollite processing with NaHS and KBX was investigated.Flotation and contact angle tests indicate that the combination of NaHS and KBX takes a better flotation performance than adding NaHS or KBX alone.Thermodynamic analysis,X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared(FTIR) results confirm the stronger chemisorption of KBX occurs on the oxidized carrollite surface with NaHS,which is beneficial to remove the cobalt oxides,thus contributing to the superior floatability.Interestingly,less elemental sulfur was observed on the carrollite surface as the interaction of NaHS and KBX than adding NaHS alone.It suggests that elemental sulfur is not the main contributor to the restored floatability of oxidized carrollite through sulfidisation.This study provided a new perspective to correlate the surface species with xanthate adsorption and oxidized carrollite flotation through determining the various intermediate products.展开更多
文摘Xanthates are organic synthesized substances with a potentially wide range of applications. They may serve as essential components of many compounds or materials that also play a vital role in various industrial and socio-economic processes. Addressing the question of the use of xanthates without considering their toxicity, and their decomposition process and products would be ecologically and healthily less sustainable. To date, related information is still dispersed and less known to the public. Therefore, this work provides a comprehensive overview of the existing information on the essentiality, fate, ecotoxicity, and health effects of xanthates and associated compounds. According to available information from scientific, technical, and professional circles, xanthates are diverse, usually with a carbon chain of two to six carbon atoms. They play a crucial role in the sectors of the mining and mineral processing industry, agriculture, wastewater treatment, metal protection, rubber vulcanization, the pharmaceutical industry, and medicine. Xanthates’ degradation under different factors and mechanisms, which determine their fate in the environment, leads to the formation of toxic substances, mainly carbon disulfide, carbonyl sulfide, hydrogen sulfide, and hydrogen peroxide. Xanthates and xanthates degradation products are seriously hazardous to humans, animals, soil and aquatic organisms, enzymatic system, etc. Simultaneous exposure to xanthates and metals results in the magnification or reduction of their toxicity level, depending on the exposed organisms. Such toxicological dimensions should attract more scientific and public attention for more safe production, use, storage, and disposal of xanthates. Due to the high affinity of xanthates for metal, xanthates-modified compounds are efficient metal chelating agents. Such a property should be explored to develop potentially low-cost and effective alternatives for metal removal and recovery from contaminated media. The same applies to developing appropriate methods for the evaluation and management of the simultaneous presence of xanthates and metals in the environment.
基金financially supported by the State Key Development Program for Basic Research of China (No.2014CB643402)the Collaborative Innovation Center for Clean and Efficient Utilization of Strategic Metal Mineral Resources of Central South University
文摘The flotation of hemimorphite using the S(Ⅱ)–Pb(Ⅱ)–xanthate process,which includes sulfidization with sodium sulfide,activation by lead cations,and subsequent flotation with xanthate,was investigated.The flotation results indicated that hemimorphite floats when the S(Ⅱ)–Pb(Ⅱ)–xanthate process is used; a maximum recovery of approximately 90% was obtained.Zeta-potential,contact-angle,scanning electron microscopy–energy-dispersive spectrometry(SEM–EDS),and diffuse-reflectance infrared Fourier transform spectroscopy(DRIFTS) measurements were used to characterize the activation products on the hemimorphite surface and their subsequent interaction with sodium butyl xanthate(SBX).The results showed that a Zn S coating formed on the hemimorphite surface after the sample was conditioned in an Na2 S solution.However,the formation of a Zn S coating on the hemimorphite surface did not improve hemimorphite flotation.With the subsequent addition of lead cations,Pb S species formed on the mineral surface.The formation of the Pb S species on the surface of hemimorphite significantly increased the adsorption capacity of SBX,forming lead xanthate(referred to as chemical adsorption) and leading to a substantial improvement in hemimorphite flotation.Our results indicate that the addition of lead cations is a critical step in the successful flotation of hemimorphite using the sulfidization–lead ion activation–xanthate process.
基金Project(50774100)supported by the National Natural Science Foundation of China
文摘Preparation of orange peel xanthate and its adsorption behaviors of five heavy metals(Cu 2+ ,Cd 2+ ,Pb 2+ ,Zn 2+ and Ni 2+ ) were studied.FTIR spectra,Zeta potentials and TG analysis were used to characterize prepared orange peel xanthate.Effects of various parameters including equilibrium pH,initial metal ion concentration and adsorption time on the adsorption processes for the five metal ions were investigated.It was found that for all five metal ions,the adsorption isotherms agreed Langmuir model very well and the maximum adsorption capacities of Cu2 +,Cd 2+,Pb 2+,Zn 2+and Ni 2+were obtained as 77.60,76.57,218.34,49.85 and 15.45 mg/g,respectively.All adsorption processes can attain equilibrium within 20 min and kinetics was well fitted by psesudo-second order equation.It is proposed that the adsorption mechanism was complexation.
文摘Wolframite notation with benzyl arsonic acid and sodium butyl xanthate is studied,at first.It shows the efficiency of mineral processig is good when the two agents are added together.Then the synergism of sodium butyl xanthate and benzyl arsonic acid is studied also by HPLC.
文摘A subbituminous coal was oxidized with air at 150℃on a fixed bed for 4 h and xanthated with carbondisulfide in a basic solution,at 30 or 5-10℃.This xanthated coal was evaluated for the removal of Hg^(2+)and Cd^(2+)from 7,000 mg/L aqueous solutions;metal concentrations were detemmined by atomic absorption spectrometry.The ionexchange of the xanthated coal was compared against those of the original subbituminous coal,a sulfonated subbituminouscoal,activated carbon,commercial activated carbon,and commercial synthetic resin.The commercial synthetic resinshowed the highest exchange capacity(concentration factor 98%)followed by the xanthated coal(concentration factor 96%).The retention of cadmium on the sulfonated subbituminous coal was lower(exchange capacity 0.56 meq/g)thanthat of xanthated coals(1.85±0.09 meq/g).Our xanthated coal showed a better Cd^(2+)removal(8l%o against 15%)than anon preoxidized 40-h-xanthated coal,which shows that oxidation of coal increased the amount of oxygenated groups whichenhanced xanthation.
文摘Three HPLC methods for the separation and determination of xanthate mixtures are described.The chromatographic behaviours,advantages and application ranges of various:methods have been discussed in detail.A calculation method for determining the results of individual xanthates from the complicated chromatographic peaks of xanthate mixtures is presented.The limits of detection are 0.15-2.0ng.
文摘Cobalt isopropyl xanthate thin films (CXTFs) were deposited via chemical bath deposition onto different substrates:commercial glass (CG), indium tin oxide (ITO), and poly(methyl methacrylate) (PMM). Isopropyl xanthate was synthesized according to a method described in the literature. The cobalt nitrate and isopropyl xanthate were mixed in a beaker, which allowed the thin films to be deposited via a simple ion-ion mechanism. The transmission, reflectivity, refractive index, dielectric constant, and optical conductivity were investigated for various thin films coated onto different substrates. An ultraviolet-visible spectrophotometer was used to measure the optical properties of the thin films. The lowest value of the transmission and the highest value of the refractive index were observed for the thin films deposited onto PMM. The structure of the cobalt xanthate was characterized by Fourier transform infrared (FTIR) spectroscopy, which was measured using a Perkin-Elmer Spectrum 400 spectrometer. The stretching vibration of the Co-S bonds was observed at 359 cm^-1 in the FTIR spectrum of the CXTFs.
文摘A simple and fast ultraviolet spectrophotometric method was used to determineselenium (Ⅳ) through the formation, separaion and quantitative determination of potassium butylxanthae -selenium complex. The complex absorbed light sharply at 375 nm. The optimum acidity ofthe complex formation was between pH 3.4 - 4.0. The absorption value was no change in 120 minutesafter the comlex was extracted by Carbon tetraChioride. The sensitivity of the colour reation was 0.2ng cm-2, The content of selenimp (Ⅳ) was within 0-30 μg and linear rclation was good,Y=0.07X+0.025, relevent coefficient r=0.9997. A great quantity of I, Cu, Co, the and SO4-2, PO4-3contained in .the Sample had no effect on the results ofdetenninion when seldsum was determined.When content of Fe was over l00gμg/ml and Zn was over 180μg/ml, there was diotance to the determination, but the disturbance was rem0ved by adding EDTA. When making use of the method todetermine containin seldsum additivef Cv =6.85, rate of recovery was 97.2%, wild jujubef;Cv=3.22,rate of recovery was 90. 1%, soil Samlef Cv=4.64, rate of recovery was 86.2%. The method for sensitivity measured was apprtoate to 2, 3-diamino naphthalene (DAN) fluorescence method.
文摘Fifteen M(S2COR)n complexes were prepared.According to the data provided by IR,UV-Vis absorption spectrometry and X-ray diffraction,this paper covers the relationship between molecular structures of xanthate complexes and their absorption spectra and a criterion of chelate stability is also proposed.The stability mechanism of xanthate chelates and related rules were investigated.
基金Ecole PolytechniqueCNRS+7 种基金DGAMNRTThe Fondation Alfred Kastlerthe Royal Commission for the Exhibition of 1851the China Research CouncilAventis(now Sanofi)Rhodia(now Solvay)Syngenta
文摘This review discusses the numerous routes to all-carbon quaternary centers based on the unique radical chemistry of xanthates. Itsummarizes the various approaches to the synthesis of tertiary xanthates then describes the intra- and intermolecular radicaladditions and combinations thereof that have so far been used to construct quaternary centers.
基金financially supported by the National Natural Science Foundation of China(Nos.51004072,51004033,51074047)the National“Twelfth Five-Year”Plan for Science&Technology Support Program of China(No.2012BAE01B02)。
文摘Xanthated crosslinked chitosan(XCCS) resin prepared under microwave irradiation were used for adsorbing Au(Ⅲ) ions in hydrochloric acid medium.The influence of pH and temperature on the adsorption capacity of XCCS was investigated.The original XCCS and the loaded XCCS were characterized by scanning electron microscope(SEM) and X-ray diffraction(XRD),respectively.The results indicate that the XCCS has ability to adsorb Au(Ⅲ) ions and the maximum adsorption capacity of Au(Ⅲ) ions on XCCS is observed at pH 1 and 20℃.The data of batch adsorption tests are fitted to kinetic models and isotherm models,respectively.The kinetics of adsorption process is found to follow pseudo-second-order kinetic rate model,and equilibrium data agree very well with the Langmuir model.Thermodynamic calculation of the Au(Ⅲ) ions adsorption process indicates that the adsorption process is spontaneous and endothermic.
基金supported by the National Natural Science Foundation of China(Nos.21877088.22171230)China Postdoctoral Science Foundation(No.2016M602861).
文摘Nano-drug delivery systems with multiple stimulus-responsive capabilities have superior response performance and efficient drug release.Nevertheless,it is sophisticated to construct multiple stimulus-responsive systems where the two or more functional groups need to be introduced simultaneously.Xanthate,one functional group with pH and H2O2 stimulus responsiveness,has significant potential applications for building dual-responsive drug delivery system.Herein,we present a novel dual stimuli-responsive supramolecular drug delivery system by using sodium xanthate derivative(SXD)as guest molecule and quaternary ammonium capped pillar[5]arene(QAP5)as host molecule through host-guest interaction on the basis of electrostatic interaction.The amphiphile QAP5⊃SXD could self-assemble into vesicles to efficiently load the anti-cancer drug DOX.The experimental results showed that QAP5⊃SXD nanoparticles could achieve efficient drug delivery and controlled release in the tumor microenvironment.Cytotoxicity experiments proved that DOX@QAP5⊃SXD nanoparticles could significantly improve the anticancer efficiency of free DOX on cancer cells.The present study provides an efficient strategy to develop supramolecular nanocarriers with dual-responsiveness in one functional group for controlled drug release.
基金supported by the National Nature Science Foundation of China(Nos.51274104,50874052)National Key Basic Research Program of China(973,No.2011CB933700)
文摘The adsorption behavior of butyl xanthate on the surface of lead oxide was investigated using continuous online in situ attenuated total reflectance Fourier transform infrared(ATR-FTIR) spectroscopy technique and two dimensional(2D) correlation analysis.The adsorbed layer studied was prepared by coating α-PbO particles onto the surfaces of the ZnSe crystal.The appearance of spectral peaks at 1203 cm^-1,1033 cm^-1 and their red shift indicated the formation and aggregation of xanthate at the surface of α-PbO.According to 1R intensity changes after rinsing with deionized water and a NaOH solution,the adsorption was proved to be a chemisorption type.The competition between xanthate and OH^- for the surfaces leads to desorption of xanthate at higher pH.The technique of 2D correlation ATR-FTIR spectroscopy was used to evaluate the changing order of spectral intensities in the adsorption process,and the results indicated that xanthate micelles were formed at the surfaces.The adsorption kinetics of butyl xanthate was found to be a pseudo-second-order reaction model and the adsorption capacity of butyl xanthate at α-PbO was as high as 281 mg g^-1 after 150 min.
基金Supported by the National Natural Science Foundation of China(Nos.21071005, 50975002) and the Natural Science Foundation of the Education Bureau of Anhui Province, China(No.K J2011A054).
文摘A new ruthenium complex containing bidentate xanthate ligands was synthesized in a good yield. This complex was characterized by elemental analysis, proton nuclear magnetic resonance(tH NMR), Fourier transform infrared(FTIR) and UV-Vis spectroscopies. The cyclic voltammetry of the complex revealed one quasi-redox wave centered at Ru(III)/Ru(II) couple, indicating its catalytic potential. So the preparation of a glass carbon electrode modified with ruthenium xanthate complex and its electrocatalytic activity toward the oxidation of tryptophan(Trp) were also studied. The experimental results show that the modified electrode had excellent electrocatalytic activity for the oxidation of tryptophan. Moreover, under the optimized conditions, the oxidation peak current was propor- tional to tryptophan concentration in a range of 2.5×10-7 to 5.0× 10-5 mol/L with a correlation coefficient of 0.9928 and a detection limit of 8.3 × 10-8 mol/L(S/N=3). Using the proposed method, tryptophan was successfully determined in pharmaceutical samples with standard addition method.
基金Sumitomo Metal Mining Co.,Ltd.,Japan International Cooperation Agency(JICA),and a Grant-inAid for Science Research(JSPS KAKENHI)from the Japan Society for the Promotion of Science(JSPS)(Nos.JP22K14636,JP22H00310 and JP19H02659)This work was partly supported by Advanced Research Infrastructure for Materials and Nanotechnology(No.JPMXP1222KU1009)in Japan sponsored by the Ministry of Education,Culture,Sports,Science and Technology(MEXT),Japan.
文摘Enargite is typically associated with chalcocite.Owing to the similarity in the flotation behaviors of these minerals,both minerals are reported to concentrate in the conventional flotation circuit.However,inorganic arsenic in enargite can decrease the copper concentrate quality and increase the operating cost of processing this concentrate.Separating these minerals is important for cleaner copper production to avoid these effects.In this context,this study investigated the effect of hydrogen peroxide(H_(2)O_(2))treatment on the flotation behavior of chalcocite and enargite.Flotation tests of pure and mixed minerals indicated that H_(2)O_(2)treatment reduced the floatability of chalcocite and enargite by forming sulfate and copper hydroxide on their surfaces.Despite the detrimental effect of the H_(2)O_(2)treatment,there was a narrow window of H_(2)O_(2)concentration for separating both minerals,in which enargite floated and chalcocite was depressed.This selective flotation behavior was caused by the rapid adsorption of potassium amyl xanthate(KAX)and lower surface oxidation of enargite compared with that of chalcocite.
基金the Project funded by Ten Thousand Talent Plans for Young Top-notch Talents of Yunnan Province (Grant No. YNWR-QNBJ-2018-051)。
文摘The direct sulfidization of cuprite is inefficient because cuprite is a copper-oxide mineral with a strong surface hydrophilicity.In this study,oxidant was used to modify cuprite surfaces to regulate the sulfidization of cuprite.Microflotation tests showed that the flotation recovery of pre-oxidized cuprite was nearly25% higher than that of direct sulfidization flotation,which indicates that the cuprite surface activity was enhanced after pre-oxidation by Cu(Ⅰ) species(weak affinity with sulfur ions) transformation to Cu(Ⅱ)species(strong affinity with sulfur ions).Zeta potential,scanning electron microscopy-energy dispersive X-ray spectroscopy,X-ray photoelectron spectroscopy,and time-of-flight secondary ion mass spectrometry results showed that pre-oxidation improved cuprite sulfidization and promoted the formation of copper-sulfide species on the cuprite surfaces.The mineral surface stability and thus,xanthate species adsorption on the cuprite surfaces were improved.The surface-adsorption measurements and infrared spectroscopy showed that a large amount of xanthate species was adsorbed onto the sulfidized cuprite surfaces after pre-oxidation,which enhanced the cuprite hydrophobicity and improved the cuprite flotation.
基金supported by Universidad Autónoma de San Luis Potosí(No.PROMEP/UASLP/12/CA15)
文摘Comparative voltammetry and differential double-layer capacitance studies were performed to evaluate interfacial interactions between cnalcopyrite(CuFeS2) and n-isopropyl xanthate(X) in the presence of ammonium bisulfite/39wt%SO2 and caustic starch at different pH values.Raman spectroscopy,Fourier transform infrared(FTIR) spectroscopy,contact angle measurements,and microflotation tests were used to establish the type and extent of xanthate adsorption as well as the species involved under different mineral surface conditions in this study.The results demonstrate that the species that favor a greater hydrophobicity of chalcopyrite are primarily CuX and S^0,whereas oxides and hydroxides of Cu and Fe as well as an excess of starch decrease the hydrophobicity.A conditioning of the mineral surface with ammonium bisulfite/39wt%SO2 at pH 6 promotes the activation of surface and enhances the xanthate adsorption.However,this effect is diminished at pH ≥ 8,when an excess of starch is added during the preconditioning step.
基金supported by the Innovation Academy for Green Manufacture, Chinese Academy of Sciences (IAGM-2019A08)。
文摘The surface species transformation of oxidized carrollite processing with NaHS and KBX was investigated.Flotation and contact angle tests indicate that the combination of NaHS and KBX takes a better flotation performance than adding NaHS or KBX alone.Thermodynamic analysis,X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared(FTIR) results confirm the stronger chemisorption of KBX occurs on the oxidized carrollite surface with NaHS,which is beneficial to remove the cobalt oxides,thus contributing to the superior floatability.Interestingly,less elemental sulfur was observed on the carrollite surface as the interaction of NaHS and KBX than adding NaHS alone.It suggests that elemental sulfur is not the main contributor to the restored floatability of oxidized carrollite through sulfidisation.This study provided a new perspective to correlate the surface species with xanthate adsorption and oxidized carrollite flotation through determining the various intermediate products.