To achieve efficient flotation separation of brucite and calcite,flotation separation experiments were conducted on two minerals using dodecylamine(DDA)as the collector and potassium dihydrogen phosphate(PDP)as the re...To achieve efficient flotation separation of brucite and calcite,flotation separation experiments were conducted on two minerals using dodecylamine(DDA)as the collector and potassium dihydrogen phosphate(PDP)as the regulator.The action mechanism of DDA and PDP was explored through contact angle measurement,zeta potential detection,solution chemistry calculation,FTIR analysis,and XPS detection.The flotation results showed that when DDA dosage was 35 mg/L and PDP dosage was 40 mg/L,the maximum floating difference between brucite and calcite was 79.81%,and the selectivity separation index was 6.46.The detection analysis showed that the main dissolved component HPO_(4)^(2−)of PDP is selectively strongly adsorbed on the Ca site on the surface of calcite,promoting the adsorption of the main dissolved component RNH_(3)^(+)of DDA on calcite surface,while brucite is basically not affected by PDP.Therefore,PDP is an effective regulator for the reverse flotation separation of brucite and calcite in DDA system.展开更多
This study investigated the effects of H2O2 treatment on xanthate interaction and flotation separation of chalcopyrite and pyrite by making use of a series of laboratory flotation experiments and surface analysis tech...This study investigated the effects of H2O2 treatment on xanthate interaction and flotation separation of chalcopyrite and pyrite by making use of a series of laboratory flotation experiments and surface analysis techniques.Flotation test results showed that H2O2 treatment influenced the flotation behaviors of the two minerals;however,flotation of pyrite was depressed more significantly than that of the chalcopyrite.Under well-controlled H2O2 concentration,the selective separation of chalcopyrite from pyrite was realized at pH 9.0,at which the recovery of chalcopyrite was over 84%and that of pyrite was less than 24%.Zeta potential,UV-visible and IR spectrum measurements revealed that the collector interacted differently with the two minerals after H2O2 treatment,and the surface of chalcopyrite adsorbed much greater amount of xanthate than that of the pyrite.IR and XPS analyses showed that the H2O2 treatment significantly changed the surface properties of pyrite to very hydrophilic species that inhibited the adsorption of collector and thus depressed the floatability of pyrite.While,the surface of chalcopyrite remained mildly inert to H2O2,as a result,the adsorption of xanthate and its oxidation to dixanthogen were very effective,which enhanced the flotation of chalcopyrite.展开更多
Fixed carrier membrane exhibits attractive CO2 permeance and selectivity due to its transport mechanism of reaction selectivity （facilitated transport）. However, its performance needs improvement to meet cost target...Fixed carrier membrane exhibits attractive CO2 permeance and selectivity due to its transport mechanism of reaction selectivity （facilitated transport）. However, its performance needs improvement to meet cost targets for CO2 capture. This study attempts to develop membranes with multiple permselective mechanisms in order to enhance CO2 separation performance of fixed carder membrane. In this study, a novel membrane with multiplepermselective mechanisms of solubility selectivity and reaction selectivity was developed by incorporating CO2-selective adsorptive silica nanoparticles in situ into the tertiary amine containing polyamide membrane formed by interfacial polymerization （IP）. Various techniques were employed to characterize the polyamide and polyam-ide-silica composite membranes. The TGA result shows that nanocomposite membranes exhlbit superior-thermal stability than pure polyamide membranes. In addition, gas permeation experiments show that both nanocomposite membranes have larger CO2 permeance than pure polyamide membranes. The enhanced CO2/N2 separation performance for nanocomposite membranes is mainly due to the thin film thickness, and multiple permselective mechanisms of solubility selectivity and reaction selectivity.展开更多
To separate MA （Am, Cm） and some fission product elements （FPs） such as Tc, Pd, Cs and Sr from high level liquid waste （HLLW） systematically, we have been studying an advanced aqueous partitioning process, which...To separate MA （Am, Cm） and some fission product elements （FPs） such as Tc, Pd, Cs and Sr from high level liquid waste （HLLW） systematically, we have been studying an advanced aqueous partitioning process, which uses selective adsorption as the separation method. For this process, we prepared several novel adsorbents which were immobilized in a porous sili- c^polymer composite support （SiO2-P）. Adsorption and separation behavior of various elements was studied experimentally in detail. Small scale separation tests using simulated HLLW solutions were carried out. Pd（II） was strongly adsorbed by the AR-01 anion exchanger and effectively eluted off by using thiourea. Successful separation of Pd（ll） from simulated HLLW was achieved. Te（VII） also exhibited strong adsorption on AR-01 and could be eluted off by using U（IV） as a reductive eluent. Am（Ⅲ） presented significantly high adsorbability and selectivity onto R-BTP/SiOz-P adsorbents over various FPs including Ln（Ⅲ）. The R-BTP adsorbents were fairly stable in 3 M HNO3, but instable against 7-irradiation-3M HNO3. An advanced par- titioning process consisting of three separation columns for the target elements separation from HLLW was proposed and the obtained experiment results indicated that the proposed process is essentially feasible.展开更多
Fast migration and efficient spatial separation of photogenerated charges in photocatalytic materials are indispensable to efficient solar water splitting reactions.Here,we construct a three-phase heterostructure of C...Fast migration and efficient spatial separation of photogenerated charges in photocatalytic materials are indispensable to efficient solar water splitting reactions.Here,we construct a three-phase heterostructure of CdS/PbTiO_(3)/TiO_(2)by selectively depositing CdS and TiO_(2)at oppositely poled crystal facets of PbTiO_(3)using single-domain ferroelectric PbTiO_(3).The heterostructure has matching band edge alignments and strong interfacial connections at different moieties.The heterostructure combines the interfacial electrical and ferroelectric fields because of their peculiar microstructures,which provide a strong driving force throughout the whole bulk to separate photogenerated charges.Almost two orders of magnitude improvement of visible-light-driven photocatalytic H_(2) production has been realized in CdS/PbTiO_(3)/TiO_(2)compared with bare PbTiO_(3)/TiO_(2),showing the efficiency of charge separation in the heterostructure.The idea of combining ferroelectrics with potential light capture semiconductor provides a paradigm to accurately design charge migration pathways,bringing a step closer to efficient solar water splitting.展开更多
Direct separation of Xe and Kr from air or used nuclear fuel(UNF)off-gas by means of porous adsorbents is of industrial importance but is a very challenging task.In this work,we show a robust metal-organic framework(M...Direct separation of Xe and Kr from air or used nuclear fuel(UNF)off-gas by means of porous adsorbents is of industrial importance but is a very challenging task.In this work,we show a robust metal-organic framework(MOF),namely ECUT-60,which renders not only high chemical stability,but also unique structure with multiple traps.This leads to the ultrahigh Xe adsorption capacity,exceeding most reported porous materials.Impressively,this MOF also enables high selectivity of Xe over Kr,CO2,O2,and N2,leading to the high-performance separation for trace quantitites of Xe/Kr from a simulated UNF reprocessing off-gas.The separation capability has been demonstrated by using dynamic breakthrough experiments,giving the record Xe uptake up to 70.4 mmol/kg and the production of 19.7 mmol/kg pure Xe.Consequently,ECUT-60 has promising potential in direct production of Xe from UNF off-gas or air.The separation mechanism,as unveiled by theoretical calculation,is attributed to the multiple traps in ECUT-60 that affords rigid restrict for Xe atom via van der Waals force.展开更多
基金the General Program of the National Natural Science Foundation of China(Nos.51974064,52174239)the National Key R&D Program of China(No.2021YFC2902400)the Outstanding Postdoctoral Program of Jiangsu Province,China(No.2022ZB521).
文摘To achieve efficient flotation separation of brucite and calcite,flotation separation experiments were conducted on two minerals using dodecylamine(DDA)as the collector and potassium dihydrogen phosphate(PDP)as the regulator.The action mechanism of DDA and PDP was explored through contact angle measurement,zeta potential detection,solution chemistry calculation,FTIR analysis,and XPS detection.The flotation results showed that when DDA dosage was 35 mg/L and PDP dosage was 40 mg/L,the maximum floating difference between brucite and calcite was 79.81%,and the selectivity separation index was 6.46.The detection analysis showed that the main dissolved component HPO_(4)^(2−)of PDP is selectively strongly adsorbed on the Ca site on the surface of calcite,promoting the adsorption of the main dissolved component RNH_(3)^(+)of DDA on calcite surface,while brucite is basically not affected by PDP.Therefore,PDP is an effective regulator for the reverse flotation separation of brucite and calcite in DDA system.
基金Projects(51704329,51705540) supported by the National Natural Science Foundation of ChinaProject(2015CX005) supported by the Innovation Driven Plan of Central South University,China+1 种基金Project(B14034) supported by the National “111” Project,ChinaProject(2018TP1002) supported by the Collaborative Innovation Center for Clean and Efficient Utilization of Strategic Metal Mineral Resources,China
文摘This study investigated the effects of H2O2 treatment on xanthate interaction and flotation separation of chalcopyrite and pyrite by making use of a series of laboratory flotation experiments and surface analysis techniques.Flotation test results showed that H2O2 treatment influenced the flotation behaviors of the two minerals;however,flotation of pyrite was depressed more significantly than that of the chalcopyrite.Under well-controlled H2O2 concentration,the selective separation of chalcopyrite from pyrite was realized at pH 9.0,at which the recovery of chalcopyrite was over 84%and that of pyrite was less than 24%.Zeta potential,UV-visible and IR spectrum measurements revealed that the collector interacted differently with the two minerals after H2O2 treatment,and the surface of chalcopyrite adsorbed much greater amount of xanthate than that of the pyrite.IR and XPS analyses showed that the H2O2 treatment significantly changed the surface properties of pyrite to very hydrophilic species that inhibited the adsorption of collector and thus depressed the floatability of pyrite.While,the surface of chalcopyrite remained mildly inert to H2O2,as a result,the adsorption of xanthate and its oxidation to dixanthogen were very effective,which enhanced the flotation of chalcopyrite.
基金Supported by the National Natural Science Foundation of China （20836006）, the National Basic Research Program （2009CB623405）, the Science ＆ Technology Pillar Program of Tianjin （10ZCKFSH01700）, the Programme of Introducing Talents of Discipline to Universities （B06006）, and the Cheung Kong Scholar Program for Innovative Teams of the Ministry of Education （IRT0641）.
文摘Fixed carrier membrane exhibits attractive CO2 permeance and selectivity due to its transport mechanism of reaction selectivity （facilitated transport）. However, its performance needs improvement to meet cost targets for CO2 capture. This study attempts to develop membranes with multiple permselective mechanisms in order to enhance CO2 separation performance of fixed carder membrane. In this study, a novel membrane with multiplepermselective mechanisms of solubility selectivity and reaction selectivity was developed by incorporating CO2-selective adsorptive silica nanoparticles in situ into the tertiary amine containing polyamide membrane formed by interfacial polymerization （IP）. Various techniques were employed to characterize the polyamide and polyam-ide-silica composite membranes. The TGA result shows that nanocomposite membranes exhlbit superior-thermal stability than pure polyamide membranes. In addition, gas permeation experiments show that both nanocomposite membranes have larger CO2 permeance than pure polyamide membranes. The enhanced CO2/N2 separation performance for nanocomposite membranes is mainly due to the thin film thickness, and multiple permselective mechanisms of solubility selectivity and reaction selectivity.
基金supported by the National Natural Science Foundation of China (91026019,91126006)
文摘To separate MA （Am, Cm） and some fission product elements （FPs） such as Tc, Pd, Cs and Sr from high level liquid waste （HLLW） systematically, we have been studying an advanced aqueous partitioning process, which uses selective adsorption as the separation method. For this process, we prepared several novel adsorbents which were immobilized in a porous sili- c^polymer composite support （SiO2-P）. Adsorption and separation behavior of various elements was studied experimentally in detail. Small scale separation tests using simulated HLLW solutions were carried out. Pd（II） was strongly adsorbed by the AR-01 anion exchanger and effectively eluted off by using thiourea. Successful separation of Pd（ll） from simulated HLLW was achieved. Te（VII） also exhibited strong adsorption on AR-01 and could be eluted off by using U（IV） as a reductive eluent. Am（Ⅲ） presented significantly high adsorbability and selectivity onto R-BTP/SiOz-P adsorbents over various FPs including Ln（Ⅲ）. The R-BTP adsorbents were fairly stable in 3 M HNO3, but instable against 7-irradiation-3M HNO3. An advanced par- titioning process consisting of three separation columns for the target elements separation from HLLW was proposed and the obtained experiment results indicated that the proposed process is essentially feasible.
基金the National Key R&D Program of China(2021YFA1500800)the National Natural Science Foundation of China(51825204,52120105003,and 52072379).
文摘Fast migration and efficient spatial separation of photogenerated charges in photocatalytic materials are indispensable to efficient solar water splitting reactions.Here,we construct a three-phase heterostructure of CdS/PbTiO_(3)/TiO_(2)by selectively depositing CdS and TiO_(2)at oppositely poled crystal facets of PbTiO_(3)using single-domain ferroelectric PbTiO_(3).The heterostructure has matching band edge alignments and strong interfacial connections at different moieties.The heterostructure combines the interfacial electrical and ferroelectric fields because of their peculiar microstructures,which provide a strong driving force throughout the whole bulk to separate photogenerated charges.Almost two orders of magnitude improvement of visible-light-driven photocatalytic H_(2) production has been realized in CdS/PbTiO_(3)/TiO_(2)compared with bare PbTiO_(3)/TiO_(2),showing the efficiency of charge separation in the heterostructure.The idea of combining ferroelectrics with potential light capture semiconductor provides a paradigm to accurately design charge migration pathways,bringing a step closer to efficient solar water splitting.
基金supported by the National Natural Science Foundations of China(21966002 and 21871047)the Natural Science Foundation of Jiangxi Province(20181ACB20003)+1 种基金the Training Program for Academic and Technical Leaders of Major Disciplines in Jiangxi Province(20194BCJ22010)the Graduate Innovation Project of East China University of Technology(DHYC-202023)。
文摘Direct separation of Xe and Kr from air or used nuclear fuel(UNF)off-gas by means of porous adsorbents is of industrial importance but is a very challenging task.In this work,we show a robust metal-organic framework(MOF),namely ECUT-60,which renders not only high chemical stability,but also unique structure with multiple traps.This leads to the ultrahigh Xe adsorption capacity,exceeding most reported porous materials.Impressively,this MOF also enables high selectivity of Xe over Kr,CO2,O2,and N2,leading to the high-performance separation for trace quantitites of Xe/Kr from a simulated UNF reprocessing off-gas.The separation capability has been demonstrated by using dynamic breakthrough experiments,giving the record Xe uptake up to 70.4 mmol/kg and the production of 19.7 mmol/kg pure Xe.Consequently,ECUT-60 has promising potential in direct production of Xe from UNF off-gas or air.The separation mechanism,as unveiled by theoretical calculation,is attributed to the multiple traps in ECUT-60 that affords rigid restrict for Xe atom via van der Waals force.
