The redox potentials of xanthate/dixanthogen (dithiocarbonate/di dithiocarbonate, DTC/(DTC) 2) and trithiocarbonate/di trithiocarbonate (TTC/(TTC) 2) couples have been measured for the potassium salts. The spectroscop...The redox potentials of xanthate/dixanthogen (dithiocarbonate/di dithiocarbonate, DTC/(DTC) 2) and trithiocarbonate/di trithiocarbonate (TTC/(TTC) 2) couples have been measured for the potassium salts. The spectroscopic characteristics of these sulfide mineral collectors were determined by FTIR and UV analysis. Electrochemically controlled contact angle measurements at a pyrite surface provided the basis to analyze the effect of the functional group ( O CS 2 versus S CS 2) on the hydrophobic surface state. Results from this preliminary examination are discussed with respect to the nature of collector adsorption and the pyrite flotation response.展开更多
This work focuses on the organic depressant,disodium bis(carboxymethyl)trithiocarbonate(DBT),as a selectivedepressant in copper?molybdenum sulfide flotation separation.Micro-flotation,Zeta potential,FTIR and XPS measu...This work focuses on the organic depressant,disodium bis(carboxymethyl)trithiocarbonate(DBT),as a selectivedepressant in copper?molybdenum sulfide flotation separation.Micro-flotation,Zeta potential,FTIR and XPS measurements werecarried out to investigate the selective depression mechanism of DBT on chalcopyrite.Zeta potential and FTIR measurementsrevealed that DBT had higher affinity for chalcopyrite than molybdenite and the XPS results of chalcopyrite before and aftertreatment with DBT further proved that DBT adsorbed on chalcopyrite surface.The investigation indicates that the mechanism ofDBT adsorbing on chalcopyrite is mainly physical adsorption.Locked circuit experiments were carried out and the results showedthat DBT could be considered as a cleaner option in commercial Cu?Mo flotation separation circuits.展开更多
In this paper, bulk flotation followed by separation was investigated to concentrate purified molybdenite product from Jinduicheng molybdenum ores(Shanxi province, China). The bench scale tests mainly focussed on sepa...In this paper, bulk flotation followed by separation was investigated to concentrate purified molybdenite product from Jinduicheng molybdenum ores(Shanxi province, China). The bench scale tests mainly focussed on separation of molybdenite from other sulfide minerals using the new type of depressants.The effect of each single depressant, including organic depressant-modified dextrin(MD), P-Nokes reagent(PN) and sodium trithiocarbonate(ST), and their mixtures on galena, chalcopyrite and other sulfide ores, was examined in turn by changing the concentrations used in cleaner flotation tests. Closed circuit experiments were carried out under the optimal condition and satisfying recovery and grade of molybdenite concentrate could be achieved(86.294% and 53.157%, respectively). A potential reagent regime was developed, with more environmental friendly and more economical advantages due to the introduction of modified dextrin.展开更多
Ultraviolet （UV）-induced graft polymerization of acrylamide （AAm） on polypropylene substrates was successfully conducted using dibenzyl trithiocarbonate （DBTTC） as photoinitiator. It was confirmed by chemical an...Ultraviolet （UV）-induced graft polymerization of acrylamide （AAm） on polypropylene substrates was successfully conducted using dibenzyl trithiocarbonate （DBTTC） as photoinitiator. It was confirmed by chemical analysis and surface morphology observation with attenuated total reflectance Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy. A possible mechanism for this graft process was presented, which suggested that, under UV irradiation, the C： S bond in DBTTC could split and abstract a hydrogen from the polypropylene surface and a surface free radical was then formed, and initiated the graft polymerization of AAm.展开更多
Sulfur-rich polymers are endowed with several enhanced features,such as high refractive index and excellent thermal and mechanical properties,owing to the incorporation of sulfur atoms into the polymer main chain.As a...Sulfur-rich polymers are endowed with several enhanced features,such as high refractive index and excellent thermal and mechanical properties,owing to the incorporation of sulfur atoms into the polymer main chain.As an important category of sulfur-rich polymers,polytrithiocarbonates can be efficiently synthesized through ring-opening polymerization(ROP)of cyclic trithiocarbonates(CTCs)mediated by 1,5,7-triazabicyclo[4.4.0]dec-5-ene(TBD)and benzyl mercaptan(BnSH).However,the mechanistic investigations of this reaction are limited.In this study,we attempted to understand this reaction by simulating chain initiation,propagation,and termination in the ROP of CTCs using density functional theory(DFT)calculations.As demonstrated,the acceleration of the ROP ofδ-CTC by BnSH can be attributed to the smaller size of BnS-compared to TBD when nucleophilic attacking,and[TBDH]+enhancing the interaction with the monomer and stabilizing the generated active species in the initiating process.In addition,the ability of BnSH to tune the topological structures of the final polymers is ascribed to the suppressed transesterification between the thiolate species and the first trithiocarbonate unit initiated by BnS-.Furthermore,the limitations that hinder the ROP of five-and six-membered CTCs under general conditions are the unfavored thermodynamic factors,wherein the ROP of six-membered CTC is possible below-75℃.展开更多
Main observation and conclusion Fluorescent intelligent materials have attracted wide attention because of their great potential applications.One major hurdle for the development and application of fluorescent intelli...Main observation and conclusion Fluorescent intelligent materials have attracted wide attention because of their great potential applications.One major hurdle for the development and application of fluorescent intelligent materials is the aggregation-caused quenching effect in the solid state.Herein,tetraphenylethylene-based trithiocarbonate polymers with satisfactory molecular weights(Mw up to 24900)were synthesized through a one-pot polymerization route under mild conditions.The polymers were non-emissive due to the quenching effect of the trithiocarbonate group.However,upon UV irradiation,the polymers degraded and strong emission from the tetraphenylethylene unit was observed.Such a unique property endows them with great potential applications,such as photopatterning,anti-counterfeit labels,and UV detection.展开更多
The novel cyclic trithiocarbonate was synthesized by dialkylation of trithiocarbonate anion with 2,2＇- bis（bromomethyl）biphenyl in a two-phase system using an onium salt as a phase-transfer agent. Styrene polymeriz...The novel cyclic trithiocarbonate was synthesized by dialkylation of trithiocarbonate anion with 2,2＇- bis（bromomethyl）biphenyl in a two-phase system using an onium salt as a phase-transfer agent. Styrene polymerization was carried out in the presence of cyclic trithiocarbonate （CTTC）. CTTC undergoes ring opening-polymerization and the incorporated trithiocarbonate moiety derived from CTTC performs as the reversible addition-fragmentation chain transfer （RAFT） agent. Through this mechanism, multiblock polys-tyrenes containing various narrow polydispersity blocks can be prepared.展开更多
This work presents a new approach for the fabrication of organic/inorganic nanohybrids as anticancer drugs by an intercalation method using S,S-bis（α,α′-dimethyl-α″-acetic acid） （trithiocarbonate） as a modifi...This work presents a new approach for the fabrication of organic/inorganic nanohybrids as anticancer drugs by an intercalation method using S,S-bis（α,α′-dimethyl-α″-acetic acid） （trithiocarbonate） as a modifier and two organoclays, such as reactive octadecylamine/MMT （montmorillonite） and non-reactive dimethyldidodecyl ammonium/MMT. The chemical and physical structures and the surface morphology of these covalently and non-covalently linked nanohybrids were investigated by FT-IR （Fourier translbrm infrared） spectroscopy, ^13C and ^29Si solid state NMR （nuclear magnetic resonance） spectroscopy, XRD （X-ray powder diffraction） and SEM （scanning electron microscopy） analyses, respectively. To evaluate the anticancer activities of the novel BATC/organoclay hybrids against MCF-7 breast cancer cells, a combination of different biochemical and biophysical testing techniques were used. Cell proliferation and cytotoxicity were detected in vitro using a real-time analysis. Cell death was confirmed by using apoptotic and necrotic analyses, the effects of which were detennined by the double staining and Annexin-V-FLUOS testing method. The results demonstrate that intercalated hybrid complexes containing a combination of various anticancer sites, such as free and complexed carboxyl, trithiocarbonate, amine and ammonium cations significantly induced cell death in breast cancer via their interactions with the DNA macromolecules of cancer cells by destroying the self-assemb｜ed structure of growing cells. Fabricated hybrid complexes may represent a new generation of effective and selective anticancer drug systems with a synthetic/natural origin for cancer chemotherapy.展开更多
文摘The redox potentials of xanthate/dixanthogen (dithiocarbonate/di dithiocarbonate, DTC/(DTC) 2) and trithiocarbonate/di trithiocarbonate (TTC/(TTC) 2) couples have been measured for the potassium salts. The spectroscopic characteristics of these sulfide mineral collectors were determined by FTIR and UV analysis. Electrochemically controlled contact angle measurements at a pyrite surface provided the basis to analyze the effect of the functional group ( O CS 2 versus S CS 2) on the hydrophobic surface state. Results from this preliminary examination are discussed with respect to the nature of collector adsorption and the pyrite flotation response.
基金Project(2016zzts109)supported by the Innovation Driven Plan of Central South University,ChinaProject(B14034)supported by the National 111 Project,China
文摘This work focuses on the organic depressant,disodium bis(carboxymethyl)trithiocarbonate(DBT),as a selectivedepressant in copper?molybdenum sulfide flotation separation.Micro-flotation,Zeta potential,FTIR and XPS measurements werecarried out to investigate the selective depression mechanism of DBT on chalcopyrite.Zeta potential and FTIR measurementsrevealed that DBT had higher affinity for chalcopyrite than molybdenite and the XPS results of chalcopyrite before and aftertreatment with DBT further proved that DBT adsorbed on chalcopyrite surface.The investigation indicates that the mechanism ofDBT adsorbing on chalcopyrite is mainly physical adsorption.Locked circuit experiments were carried out and the results showedthat DBT could be considered as a cleaner option in commercial Cu?Mo flotation separation circuits.
基金funding from the Innovation Driven Plan of Central South University (No.2016zzts109)the financial support from Jinduicheng Molybdenum Group Co.Ltd.(JDCMMC)
文摘In this paper, bulk flotation followed by separation was investigated to concentrate purified molybdenite product from Jinduicheng molybdenum ores(Shanxi province, China). The bench scale tests mainly focussed on separation of molybdenite from other sulfide minerals using the new type of depressants.The effect of each single depressant, including organic depressant-modified dextrin(MD), P-Nokes reagent(PN) and sodium trithiocarbonate(ST), and their mixtures on galena, chalcopyrite and other sulfide ores, was examined in turn by changing the concentrations used in cleaner flotation tests. Closed circuit experiments were carried out under the optimal condition and satisfying recovery and grade of molybdenite concentrate could be achieved(86.294% and 53.157%, respectively). A potential reagent regime was developed, with more environmental friendly and more economical advantages due to the introduction of modified dextrin.
基金This work was financed by the National Natural Science Foundation of China(No. 20474054).
文摘Ultraviolet （UV）-induced graft polymerization of acrylamide （AAm） on polypropylene substrates was successfully conducted using dibenzyl trithiocarbonate （DBTTC） as photoinitiator. It was confirmed by chemical analysis and surface morphology observation with attenuated total reflectance Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy. A possible mechanism for this graft process was presented, which suggested that, under UV irradiation, the C： S bond in DBTTC could split and abstract a hydrogen from the polypropylene surface and a surface free radical was then formed, and initiated the graft polymerization of AAm.
基金This work was supported by the National Natural Science Foundation of China(Nos.21722402,21674015,22171038)the China Postdoctoral Science Foundation(Nos.2021050,2021M690517)the Scientific Research Foundation of the Educational Department of Liaoning Province,China(No.LJKZ0848).
文摘Sulfur-rich polymers are endowed with several enhanced features,such as high refractive index and excellent thermal and mechanical properties,owing to the incorporation of sulfur atoms into the polymer main chain.As an important category of sulfur-rich polymers,polytrithiocarbonates can be efficiently synthesized through ring-opening polymerization(ROP)of cyclic trithiocarbonates(CTCs)mediated by 1,5,7-triazabicyclo[4.4.0]dec-5-ene(TBD)and benzyl mercaptan(BnSH).However,the mechanistic investigations of this reaction are limited.In this study,we attempted to understand this reaction by simulating chain initiation,propagation,and termination in the ROP of CTCs using density functional theory(DFT)calculations.As demonstrated,the acceleration of the ROP ofδ-CTC by BnSH can be attributed to the smaller size of BnS-compared to TBD when nucleophilic attacking,and[TBDH]+enhancing the interaction with the monomer and stabilizing the generated active species in the initiating process.In addition,the ability of BnSH to tune the topological structures of the final polymers is ascribed to the suppressed transesterification between the thiolate species and the first trithiocarbonate unit initiated by BnS-.Furthermore,the limitations that hinder the ROP of five-and six-membered CTCs under general conditions are the unfavored thermodynamic factors,wherein the ROP of six-membered CTC is possible below-75℃.
基金support from the National Natural Science Foundation of China(No.21788102)the Research Grants Council of Hong Kong(Nos.16305618,16304819 and C6014-2000)+2 种基金the Innovation and Technology Commission(No.ITC-CNERC14SC01)the Science and Technology Plan of Shenzhen(Nos.JCYJ20160229205601482 and JCY20170818113602462)the National Science Foundation of Guangdong Province(No,2019B121205002).
文摘Main observation and conclusion Fluorescent intelligent materials have attracted wide attention because of their great potential applications.One major hurdle for the development and application of fluorescent intelligent materials is the aggregation-caused quenching effect in the solid state.Herein,tetraphenylethylene-based trithiocarbonate polymers with satisfactory molecular weights(Mw up to 24900)were synthesized through a one-pot polymerization route under mild conditions.The polymers were non-emissive due to the quenching effect of the trithiocarbonate group.However,upon UV irradiation,the polymers degraded and strong emission from the tetraphenylethylene unit was observed.Such a unique property endows them with great potential applications,such as photopatterning,anti-counterfeit labels,and UV detection.
基金This work was supported by the National Science Foundation of China (No. 20204013).
文摘The novel cyclic trithiocarbonate was synthesized by dialkylation of trithiocarbonate anion with 2,2＇- bis（bromomethyl）biphenyl in a two-phase system using an onium salt as a phase-transfer agent. Styrene polymerization was carried out in the presence of cyclic trithiocarbonate （CTTC）. CTTC undergoes ring opening-polymerization and the incorporated trithiocarbonate moiety derived from CTTC performs as the reversible addition-fragmentation chain transfer （RAFT） agent. Through this mechanism, multiblock polys-tyrenes containing various narrow polydispersity blocks can be prepared.
文摘This work presents a new approach for the fabrication of organic/inorganic nanohybrids as anticancer drugs by an intercalation method using S,S-bis（α,α′-dimethyl-α″-acetic acid） （trithiocarbonate） as a modifier and two organoclays, such as reactive octadecylamine/MMT （montmorillonite） and non-reactive dimethyldidodecyl ammonium/MMT. The chemical and physical structures and the surface morphology of these covalently and non-covalently linked nanohybrids were investigated by FT-IR （Fourier translbrm infrared） spectroscopy, ^13C and ^29Si solid state NMR （nuclear magnetic resonance） spectroscopy, XRD （X-ray powder diffraction） and SEM （scanning electron microscopy） analyses, respectively. To evaluate the anticancer activities of the novel BATC/organoclay hybrids against MCF-7 breast cancer cells, a combination of different biochemical and biophysical testing techniques were used. Cell proliferation and cytotoxicity were detected in vitro using a real-time analysis. Cell death was confirmed by using apoptotic and necrotic analyses, the effects of which were detennined by the double staining and Annexin-V-FLUOS testing method. The results demonstrate that intercalated hybrid complexes containing a combination of various anticancer sites, such as free and complexed carboxyl, trithiocarbonate, amine and ammonium cations significantly induced cell death in breast cancer via their interactions with the DNA macromolecules of cancer cells by destroying the self-assemb｜ed structure of growing cells. Fabricated hybrid complexes may represent a new generation of effective and selective anticancer drug systems with a synthetic/natural origin for cancer chemotherapy.
