In this work, a series of coal-based active carbon （CAC） catalysts loaded by A1203 were prepared by sol-gel method and used for the simulta- neous catalytic hydrolysis of carbonyl sulfide （COS） and carbon disulfi...In this work, a series of coal-based active carbon （CAC） catalysts loaded by A1203 were prepared by sol-gel method and used for the simulta- neous catalytic hydrolysis of carbonyl sulfide （COS） and carbon disulfide （CS2） at relatively low temperatures of 30-70 ℃. The influences of calcinations temperatures and operation conditions such as： reaction temperature, 02 concentration, gas hourly space velocity （GHSV） and relative humidity （RH） were also discussed respectively. The results showed that catalysts with 5.0 wt% A1203 calcined at 300 ℃ had supe- rior activity for the simultaneous catalytic hydrolysis of COS and CS2. When the reaction temperature was above 50 ℃, catalytic hydrolysis activity of COS could be enhanced but that of CS2 was inhibited. Too high RH could make the catalytic hydrolysis activities of COS and CS2 decrease. A small amount of 02 introduction could enhance the simultaneous catalytic hydrolysis activities of COS and CS2.展开更多
The sol–gel method was used to synthesize a series of metal oxides-supported activated carbon fiber (ACF) and the simultaneous catalytic hydrolysis activity of carbonyl sulfide (COS)and carbon disulfide (CS2) at rela...The sol–gel method was used to synthesize a series of metal oxides-supported activated carbon fiber (ACF) and the simultaneous catalytic hydrolysis activity of carbonyl sulfide (COS)and carbon disulfide (CS2) at relatively low temperatures of 60°C was tested.The effects of preparation conditions on the catalyst properties were investigated,including the kinds and amount of metal oxides and calcination temperatures.The activity tests indicated that catalysts with 5 wt.%Ni after calcining at 400°C (Ni(5)/ACF(400)) had the best performance for the simultaneous catalytic hydrolysis of COS and CS2.The surface and structure properties of prepared ACF were characterized by scanning electron microscope-energy disperse spectroscopy (SEM-EDS),Brunauer–Emmett–Teller (BET),X-ray diffraction (XRD),carbon dioxidetemperature programmed desorption (CO2-TPD) and diffuse reflectance Fourier transform infrared reflection (DRFTIR).And the metal cation defects were researched by electron paramagnetic resonance (EPR) method.The characterization results showed that the supporting of Ni on the ACF made the ACF catalyst show alkaline and increased the specific surface area and the number of micropores,then improved catalytic hydrolysis activity.The DRFTIR results revealed that-OH species could facilitate the hydrolysis of COS and CS2;-COO and-C–O species could facilitate the oxidation of catalytic hydrolysate H2S.And the EPR results showed that high calcination temperature conditions provide more active reaction center for the COS and CS2 adsorption.展开更多
Photochemical production of carbonyl sulfide（COS）,carbon disulfide（CS_2） and dimethyl sulfide（DMS） was intensively studied in the water from the Aohai Lake of Beijing city.The lake water was found to be highly s...Photochemical production of carbonyl sulfide（COS）,carbon disulfide（CS_2） and dimethyl sulfide（DMS） was intensively studied in the water from the Aohai Lake of Beijing city.The lake water was found to be highly supersaturated with COS,CS_2 and DMS,with their initial concentrations of 0.91 ± 0.073 nmol/L,0.55 ± 0.071 nmol/L and 0.37 ± 0.062 nmol/L,respectively.The evident photochemical production of COS and CS_2 in the lake water under irradiation of 365 nm and 302 nm indicated that photochemical production of them might be the reason for their supersaturation.The similar dependence of wavelength and oxygen for photochemical production of COS,CS_2 and DMS implied that they might be from the same precursors.The water cage effect was found to favor COS production but inhibit CS_2and DMS formation,indicating that COS photochemical production was mainly from direct degradation of the precursors and the formation of CS_2 and DMS needed intermediates via combination of carbon-centered radicals and sulfur-centered radicals.The above assumptions were further confirmed by simulation experiments with addition of carbonyls and amino acids（cysteine and methionine）,and the photochemical formation mechanisms for COS,CS_2 and DMS in water were derived from the investigations.展开更多
The catalytic oxidization of CS2 over atmospheric particles and some oxide catalysts was explored through FT-IR, MS and a fixed-bed stainless steel reactor. The results show that atmospheric particles and some oxide c...The catalytic oxidization of CS2 over atmospheric particles and some oxide catalysts was explored through FT-IR, MS and a fixed-bed stainless steel reactor. The results show that atmospheric particles and some oxide catalysts exhibited considerable oxidizing activities for CS2 at ambient temperature. The reaction products are mainly COS and elemental sulfur, even CO2 on some catalysts. Among the catalysts, CaO has the strongest catalytic activity for oxidizing CS2. Fe2O3 is weaker than CaO. The catalytic activity for Al2O3 reduces considerably compared with the former two catalysts, and SiO2 the weakest. Atmospheric particle samples’ catalytic activity is between Fe2O3’s and Al2O3’s. The atmospheric particle sample collected mainly consists of Ca(Al2Si2O8) · 4H2O, which is also the main component of cement. COS, the main product, is formed by the catalytic oxidization of CS2 with adsorbed “molecular” oxygen over the catalysts’ surfaces. The concentration of adsorbed oxygen over catalysts’ surfaces may be the key factor contributed to the oxidizing activity. It is indicated that CS2 could be catalytically oxidized over atmospheric particles, which induced that this reaction may be another important source of atmospheric COS from CS2.展开更多
基金supported by the Ministry of Environmental Protection,Public Welfare Project(Contract No 201109034)the National Natural Science Foundation(U1137603)
文摘In this work, a series of coal-based active carbon （CAC） catalysts loaded by A1203 were prepared by sol-gel method and used for the simulta- neous catalytic hydrolysis of carbonyl sulfide （COS） and carbon disulfide （CS2） at relatively low temperatures of 30-70 ℃. The influences of calcinations temperatures and operation conditions such as： reaction temperature, 02 concentration, gas hourly space velocity （GHSV） and relative humidity （RH） were also discussed respectively. The results showed that catalysts with 5.0 wt% A1203 calcined at 300 ℃ had supe- rior activity for the simultaneous catalytic hydrolysis of COS and CS2. When the reaction temperature was above 50 ℃, catalytic hydrolysis activity of COS could be enhanced but that of CS2 was inhibited. Too high RH could make the catalytic hydrolysis activities of COS and CS2 decrease. A small amount of 02 introduction could enhance the simultaneous catalytic hydrolysis activities of COS and CS2.
基金supported by the National Key R&D Program of China (No.2018YFC0213400)the National Natural Science Foundation of China (Nos.51968034,41807373,21667015 and51708266)the Science and Technology Program of Yunnan province (No.2019FB069)。
文摘The sol–gel method was used to synthesize a series of metal oxides-supported activated carbon fiber (ACF) and the simultaneous catalytic hydrolysis activity of carbonyl sulfide (COS)and carbon disulfide (CS2) at relatively low temperatures of 60°C was tested.The effects of preparation conditions on the catalyst properties were investigated,including the kinds and amount of metal oxides and calcination temperatures.The activity tests indicated that catalysts with 5 wt.%Ni after calcining at 400°C (Ni(5)/ACF(400)) had the best performance for the simultaneous catalytic hydrolysis of COS and CS2.The surface and structure properties of prepared ACF were characterized by scanning electron microscope-energy disperse spectroscopy (SEM-EDS),Brunauer–Emmett–Teller (BET),X-ray diffraction (XRD),carbon dioxidetemperature programmed desorption (CO2-TPD) and diffuse reflectance Fourier transform infrared reflection (DRFTIR).And the metal cation defects were researched by electron paramagnetic resonance (EPR) method.The characterization results showed that the supporting of Ni on the ACF made the ACF catalyst show alkaline and increased the specific surface area and the number of micropores,then improved catalytic hydrolysis activity.The DRFTIR results revealed that-OH species could facilitate the hydrolysis of COS and CS2;-COO and-C–O species could facilitate the oxidation of catalytic hydrolysate H2S.And the EPR results showed that high calcination temperature conditions provide more active reaction center for the COS and CS2 adsorption.
基金supported through Strategic Priority Research Program projects(B)of the Chinese Academy of Sciences(No.XDB05010100)the Special Fund for Environmental Research in the Public Interest(No.201509002)the National Natural Science Foundation of China(Nos.21477142,41575121,41203070)
文摘Photochemical production of carbonyl sulfide（COS）,carbon disulfide（CS_2） and dimethyl sulfide（DMS） was intensively studied in the water from the Aohai Lake of Beijing city.The lake water was found to be highly supersaturated with COS,CS_2 and DMS,with their initial concentrations of 0.91 ± 0.073 nmol/L,0.55 ± 0.071 nmol/L and 0.37 ± 0.062 nmol/L,respectively.The evident photochemical production of COS and CS_2 in the lake water under irradiation of 365 nm and 302 nm indicated that photochemical production of them might be the reason for their supersaturation.The similar dependence of wavelength and oxygen for photochemical production of COS,CS_2 and DMS implied that they might be from the same precursors.The water cage effect was found to favor COS production but inhibit CS_2and DMS formation,indicating that COS photochemical production was mainly from direct degradation of the precursors and the formation of CS_2 and DMS needed intermediates via combination of carbon-centered radicals and sulfur-centered radicals.The above assumptions were further confirmed by simulation experiments with addition of carbonyls and amino acids（cysteine and methionine）,and the photochemical formation mechanisms for COS,CS_2 and DMS in water were derived from the investigations.
基金the Foundation of Fellow of the Ministry of Education of China.
文摘The catalytic oxidization of CS2 over atmospheric particles and some oxide catalysts was explored through FT-IR, MS and a fixed-bed stainless steel reactor. The results show that atmospheric particles and some oxide catalysts exhibited considerable oxidizing activities for CS2 at ambient temperature. The reaction products are mainly COS and elemental sulfur, even CO2 on some catalysts. Among the catalysts, CaO has the strongest catalytic activity for oxidizing CS2. Fe2O3 is weaker than CaO. The catalytic activity for Al2O3 reduces considerably compared with the former two catalysts, and SiO2 the weakest. Atmospheric particle samples’ catalytic activity is between Fe2O3’s and Al2O3’s. The atmospheric particle sample collected mainly consists of Ca(Al2Si2O8) · 4H2O, which is also the main component of cement. COS, the main product, is formed by the catalytic oxidization of CS2 with adsorbed “molecular” oxygen over the catalysts’ surfaces. The concentration of adsorbed oxygen over catalysts’ surfaces may be the key factor contributed to the oxidizing activity. It is indicated that CS2 could be catalytically oxidized over atmospheric particles, which induced that this reaction may be another important source of atmospheric COS from CS2.
