Modified ethylene-vinyl acetate copolymer(EVAM)and amino-functionalized nano-silica(NSiO_(2))par-ticles were employed as the base materials for the synthesis of the nanocomposite pour point depressant designated as EV...Modified ethylene-vinyl acetate copolymer(EVAM)and amino-functionalized nano-silica(NSiO_(2))par-ticles were employed as the base materials for the synthesis of the nanocomposite pour point depressant designated as EVAM-g-NSiO_(2).This synthesis involved a chemical grafting process within a solution system,followed by a structural characterization.Moreover,combining macro-rheological performance with microscopic structure observation,the influence of the nanocomposite pour point depressant on the rheological properties of the model waxy oil system was investigated.The results indicate that when the mass ratio of NSiO_(2) to EVAM is 1:100,the prepared EVAM-g-NSiO_(2) nanocomposite pour point depressant exhibits excellent pour point reduction and viscosity reduction properties.Moreover,the nanocomposite pour point depressant obtained through a chemical grafting reaction demonstrates structural stability(the bonding between the polymer and nanoparticles is stable).The pour points of model waxy oils doped with 500 mg/kg ethylene-vinyl acetate copolymer(EVA),EVAM,and EVAM/SiO_(2) were reduced from 34℃ to 23,20,and 21℃,respectively.After adding the same dosage of EVAM-g-NSiO_(2) nanocomposite pour point depressant,the pour point of the model wax oil decreased to 12℃ and the viscosity at 32℃ decreased from 2399 to 2396.9 mPa·s,achieving an impressive viscosity reduction rate of 99.9%.Its performance surpassed that of EVA,EVAM,and EVAM/SiO_(2).The EVAM-g-NSiO_(2) dispersed in the oil phase acts as the crystallization nucleus for wax crystals,resulting in a dense structure of wax crystals.The compact wax crystal blocks are difficult to overlap with each other,pre-venting the formation of a three-dimensional network structure,thereby improving the low-temperature flowability of the model waxy oil.展开更多
The effect of alcoholic polyethylene-vinyl acetate(EVA)product ethylene-vinyl alcohol copolymer(EVAL)on the low-temperature flow properties of model oil containing asphaltene(ASP)was investigated.The change of wax cry...The effect of alcoholic polyethylene-vinyl acetate(EVA)product ethylene-vinyl alcohol copolymer(EVAL)on the low-temperature flow properties of model oil containing asphaltene(ASP)was investigated.The change of wax crystal microscopic morphology of model oil before and after modification were examined,and the influence of asphaltene mass fraction on the rheological improvement effect of EVAL was analyzed.The composite system of EVAL and asphaltene significantly reduced the pour point,gel point,apparent viscosity,storage modulus and loss modulus of waxy oil at low temperatures.When the EVAL concentration is 400 ppm and the asphaltene mass fraction is 0.5 wt%,the synergistic effect of the two is optimal,which can reduce the pour point by 17℃and the modulus value by more than 98%.The introduction of EVAL strengthens the interaction between asphaltenes and wax crystals,forming EVALASP aggregates,which promote the adsorption of wax crystals on asphaltenes to form composite particles,and the polar groups prevent the aggregation of wax crystals and reduce the size of wax crystals,thus greatly improving the fluidity of waxy oils.展开更多
The nanocomposite EVAL-CNT was produced by chemical grafting in the solution system through the esterification of ethylene-vinyl alcohol copolymer (EVAL) and carboxylated multi-walled carbon nanotubes (O-MWCNT), and i...The nanocomposite EVAL-CNT was produced by chemical grafting in the solution system through the esterification of ethylene-vinyl alcohol copolymer (EVAL) and carboxylated multi-walled carbon nanotubes (O-MWCNT), and its structural properties were characterized. The improvement of the rheological properties of the waxy oil system by the novel pour point depressant was investigated using macroscopic rheological measurements and microscopic observations. The results showed that EVAL-CNT nanocomposite pour point depressant (PPD) could significantly reduce the pour point and improve the low temperature fluidity of crude oil and had better performance than EVAL-GO at the same addition level. The best effect was achieved at the dosing concentration of 400 ppm, which reduced the pour point by 13 ℃ and the low-temperature viscosity by 85.4%. The nanocomposites dispersed in the oil phase influenced the precipitation and crystallization of wax molecules through heterogeneous crystallization templates, which led to the increase of wax crystal size and compact structure and changed the wax crystal morphology, which had a better effect on the rheological properties of waxy oil.展开更多
Oxidative desulfurization from fuel oil is one of the important methods for deep desulfurization.The development of efficient oxidative desulfurization catalysts is crucial for improving the desulfurization performanc...Oxidative desulfurization from fuel oil is one of the important methods for deep desulfurization.The development of efficient oxidative desulfurization catalysts is crucial for improving the desulfurization performance.Successful encapsulation of phosphotungstic acid(HPW)and ionic liquid(BMImBr)inside the mesoporous cages of MIL-101(Cr)was accomplished through a combination of“bottle around ship”and“ship in bottle”methods.The obtained BMImPW@MIL-101(Cr)composite was characterized by XRD,FTIR,BET,SEM,XPS and ICP methods.Results indicated that the BMImPW@MIL-101(Cr)composites with PW^(3−) loading of 23.1–50.7 wt%were obtained,demonstrating that the“bottle around ship”method is beneficial to make full use of nanocages of MIL-101(Cr)to obtain expected high loading of active PW^(3−) .The BMImPW@MIL-101(Cr)exhibits excellent reusability with no evidence of leaching of active PW^(3−) and BMIm^(+),and well-preserved structure after successive cycles of regeneration and reuse.The significantly improved stability of BMImPW@MIL-101(Cr)as compared to HPW@MIL-101(Cr)is possibly because the leaching of the active PW^(3−) −sites can be greatly suppressed by forming large size of BMImPW owing to introduction of BMIm^(+)cation.The BMImPW@MIL-101(Cr)exhibited excellent catalytic activity for solvent free oxidative desulfurization of refractory sulfides.The enhanced oxidative desulfurization activity as compared to HPW@MIL-101(Cr)can be explained by the intimate contact of sulfides with active PW^(3−) sites owing the strong attraction of BMIm^(+)cation with the sulfides.展开更多
An efficient extraction-free oxidative desulfurization(ODS)process using a series of cross-linked polyionic liquid phosphotungstate(CLPIL-PW)catalysts is reported.The cross-linked PILs were prepared with DVB and 1-n-a...An efficient extraction-free oxidative desulfurization(ODS)process using a series of cross-linked polyionic liquid phosphotungstate(CLPIL-PW)catalysts is reported.The cross-linked PILs were prepared with DVB and 1-n-alkyl-3-vinyl imidazole hydrobromide(alkyl=ethyl,butyl,octyl,dodecyl),and were then assembled with phosphotungstic acid(H_(3)PW_(12)O_(40))to form the catalysts.The CLPIL-PWs have been applied to the oxidative removal of dibenzothiophene(DBT)from model oil with H_(2)O_(2) as an oxidant.The effects of ionic liquid(IL)cationic species,varying the DVB/IL molar ratio in the polymerization process,and varying operating conditions were investigated.The CLPIL-PWs were characterized by inductively coupled plasma(ICP)mass spectrometry,elemental analysis,scanning electron microscopy(SEM),Fourier transform infra-red(FTIR)spectroscopy,X-ray diffraction(XRD),^(13)C and^(31)P nuclear magnetic resonance(NMR)spectroscopy.The polydivinylbenzene-co-1-n-octyl-3-vinyl imidazole phosphotungstate(P(DVB-OVIm)PW)exhibited the highest DBT removal efficiency(99.9%)and remarkable recyclability,and could be reused eight times without reducing its activity.Finally,an extraction-free ODS mechanism is proposed.展开更多
The development of non-noble metal oxidation reduction catalysts(ORR)to improve microbial fuel cell(MFC)performance remains extremely challenging.Herein,the nitrogen-doped iron-based porous carbon nanotube Fe/N@MC-T O...The development of non-noble metal oxidation reduction catalysts(ORR)to improve microbial fuel cell(MFC)performance remains extremely challenging.Herein,the nitrogen-doped iron-based porous carbon nanotube Fe/N@MC-T ORR catalysts were derived from Fe/N-MOF by pyrolyzation using acetonitrile as the nitrogen precursor in a low-cost organic solvent.The Fe/N@MC-T catalysts under different pyrolysis temperatures were characterized by SEM,TEM,BET,XRD,and XPS techniques.Fe/N-MOF showed a smooth rice-like structure with a particle size of about 400×50 nm^(2).The Fe species in Fe/N@MC-T mainly exists in the form of zero-valent iron with a small amount of Fe3C.The results of electrochemical tests revealed that the onset and half-wave potentials of Fe/N@MC-700 were 0.89 V and 0.80 V,respectively,which were only slightly lower than those of the commercial Pt/C(0.92 V and 0.82 V).The MFC with Fe/N@MC-700 showed a highest power density of 864.1 mW/m^(2),which was about 2.25 times that of MFC with carbon cloth,and was slightly lower than that of MFC with Pt/C(20%)(1002.0 mW/m^(2)),which demonstrated that the Fe particles wrapped in carbon nanotubes possessed a relatively high ORR activity.展开更多
The degradation of partially hydrolyzed polyacrylamide(HPAM) found in alkaline/surfactant/polymer flooding sewage was investigated using Fenton-type reagents. Different Fenton reagent treatments for HPAM degradation w...The degradation of partially hydrolyzed polyacrylamide(HPAM) found in alkaline/surfactant/polymer flooding sewage was investigated using Fenton-type reagents. Different Fenton reagent treatments for HPAM degradation were compared. The effects of pH, hydrogen peroxide(H_(2)O_(2)), ferrous ion(Fe^(2+)), and tartaric ion(C_(4)H_(4)O_(6)^(2-)) concentrations were studied. The degradation reaction occurred within a wide range of pH(3–9). The HPAM degradation performance of photo-Fenton processes using solar light and UV were compared with that of the Fenton process. The degradation rate was found to be strongly dependent on the H_(2)O_(2)/Fe^(2+)/C_(4)H_(4)O_(6)^(2-)molar ratio. The HPAM degradation efficiency was 90%, and the chemical oxygen demand removal efficiency was 85%. HPAM could be degraded into a compound with a lower molecular weight, but it was difficult to achieve complete mineralization to CO_(2). The presence of intermediate products hindered further oxidation in the Fenton process.展开更多
The non-noble metal modified sulfated zirconia was found easy to deactivate.Herein,highly active and highly stable non-noble core-shell Ni-S_(2)O_(8)^(2−)/Al_(2)O_(3)@ZrO_(2) catalysts(Ni-SA@Z-x,x=Al content in wt%)ha...The non-noble metal modified sulfated zirconia was found easy to deactivate.Herein,highly active and highly stable non-noble core-shell Ni-S_(2)O_(8)^(2−)/Al_(2)O_(3)@ZrO_(2) catalysts(Ni-SA@Z-x,x=Al content in wt%)have been successfully prepared and investigated for n-pentane isomerization.The results showed that the core-shell Ni-SA@Z-30 provided a sustained high isopentane yield(63.1%)with little or no deactivation within 5000 min at a mild reaction pressure of 2.0 MPa,which can be attributed to the following factors:(i)carbon deposition was greatly suppressed by the large pore size and huge pore volume;(ii)the loss of sulfur entities was suppressed because the small and highly dispersed tetragonal ZrO_(2) particles can bond with the S species strongly;(iii)strong Brønsted acidity can be maintained well after the isomerization.The pore structures and acid nature of the core-shell Ni-SA@Z-x are entirely different from those of the normal structure Ni-S_(2)O_(8)^(2−)/ZrO_(2)-Al_(2)O_(3),even though the Al content and the compositions of the individual components are the same.The Al_(2)O_(3)cores endow the catalysts with high internal surface area and high mechanical strength.Meanwhile,the ZrO_(2) shell,which consists of more and smaller tetragonal ZrO_(2) particles because of the large surface area of the Al_(2)O_(3)core,promotes the formation of more stable sulfur species and stronger binding sites.展开更多
Heterojunction composites were prepared by silane coupling agent grafting from synthesized graphitic carbon nitride(g-C_(3)N_(4))and commercially available zirconia(ZrO_(2)).The samples were characterized by X-ray dif...Heterojunction composites were prepared by silane coupling agent grafting from synthesized graphitic carbon nitride(g-C_(3)N_(4))and commercially available zirconia(ZrO_(2)).The samples were characterized by X-ray diffraction(XRD),scanning electron microscopy(SEM),Fourier transform infrared(FT-IR)spectroscopy,UV-vis diffuse reflectance spectroscopy(DRS),photoluminescence(PL)spectroscopy,and electrochemical impedance spectroscopy(EIS).The photocatalytic activity of the composites was evaluated by the degradation of methylene blue(MB)under visible light irradiation.The results showed that heterojunction composites of g-C_(3)N_(4) and ZrO_(2) could be successfully prepared by coupling agent grafting.The optimal mass ratio of g-C_(3)N_(4) and ZrO_(2) was 2:1,with an activity that was 3.8 times higher than g-C_(3)N_(4) and 15.3 times higher than ZrO_(2).This was ascribed to the stronger light absorption,faster interfacial charge transfer,and lower photogenerated carrier recombination of the heterojunction composites.展开更多
Nickel phosphide-carbon-doped alumina(Ni_(2)P/Al_(2)O_(3)-C)catalysts with 10 wt.%Ni_(2)P loading were successfully prepared via a hydrothermal reduction process and the effect of reduction temperature on the hydrodes...Nickel phosphide-carbon-doped alumina(Ni_(2)P/Al_(2)O_(3)-C)catalysts with 10 wt.%Ni_(2)P loading were successfully prepared via a hydrothermal reduction process and the effect of reduction temperature on the hydrodesulfurization(HDS)performance of the as-prepared Ni_(2)P/Al_(2)O_(3)-C catalysts was investigated.The properties of the support(Al_(2)O_(3)-C)and Ni_(2)P/Al_(2)O_(3)-C catalysts were characterized by transmission electron microscopy,scanning electron microscopy,Brunauer-Emmett-Teller measurements,X-ray diffractometry,and X-ray photoelectron spectroscopy.The results indicated that the incorporation of carbon in the support aided the reduction of Ni_(2)P.With an increase in the reduction temperature,Ni and Ni_(12)P_(5) were first generated and then converted into crystalline Ni_(2)P.Furthermore,a higher reduction temperature enhanced the HDS performance of the catalyst by generating more well-dispersed active-phase crystalline Ni_(2)P.展开更多
基金supported by the National Natural Science Foundation of China(No.52076036)supported by the National Natural Science Foundation of China(No.52174020).
文摘Modified ethylene-vinyl acetate copolymer(EVAM)and amino-functionalized nano-silica(NSiO_(2))par-ticles were employed as the base materials for the synthesis of the nanocomposite pour point depressant designated as EVAM-g-NSiO_(2).This synthesis involved a chemical grafting process within a solution system,followed by a structural characterization.Moreover,combining macro-rheological performance with microscopic structure observation,the influence of the nanocomposite pour point depressant on the rheological properties of the model waxy oil system was investigated.The results indicate that when the mass ratio of NSiO_(2) to EVAM is 1:100,the prepared EVAM-g-NSiO_(2) nanocomposite pour point depressant exhibits excellent pour point reduction and viscosity reduction properties.Moreover,the nanocomposite pour point depressant obtained through a chemical grafting reaction demonstrates structural stability(the bonding between the polymer and nanoparticles is stable).The pour points of model waxy oils doped with 500 mg/kg ethylene-vinyl acetate copolymer(EVA),EVAM,and EVAM/SiO_(2) were reduced from 34℃ to 23,20,and 21℃,respectively.After adding the same dosage of EVAM-g-NSiO_(2) nanocomposite pour point depressant,the pour point of the model wax oil decreased to 12℃ and the viscosity at 32℃ decreased from 2399 to 2396.9 mPa·s,achieving an impressive viscosity reduction rate of 99.9%.Its performance surpassed that of EVA,EVAM,and EVAM/SiO_(2).The EVAM-g-NSiO_(2) dispersed in the oil phase acts as the crystallization nucleus for wax crystals,resulting in a dense structure of wax crystals.The compact wax crystal blocks are difficult to overlap with each other,pre-venting the formation of a three-dimensional network structure,thereby improving the low-temperature flowability of the model waxy oil.
基金financially supported by the National Natural Science Foundation of China(No.52076036)。
文摘The effect of alcoholic polyethylene-vinyl acetate(EVA)product ethylene-vinyl alcohol copolymer(EVAL)on the low-temperature flow properties of model oil containing asphaltene(ASP)was investigated.The change of wax crystal microscopic morphology of model oil before and after modification were examined,and the influence of asphaltene mass fraction on the rheological improvement effect of EVAL was analyzed.The composite system of EVAL and asphaltene significantly reduced the pour point,gel point,apparent viscosity,storage modulus and loss modulus of waxy oil at low temperatures.When the EVAL concentration is 400 ppm and the asphaltene mass fraction is 0.5 wt%,the synergistic effect of the two is optimal,which can reduce the pour point by 17℃and the modulus value by more than 98%.The introduction of EVAL strengthens the interaction between asphaltenes and wax crystals,forming EVALASP aggregates,which promote the adsorption of wax crystals on asphaltenes to form composite particles,and the polar groups prevent the aggregation of wax crystals and reduce the size of wax crystals,thus greatly improving the fluidity of waxy oils.
文摘The nanocomposite EVAL-CNT was produced by chemical grafting in the solution system through the esterification of ethylene-vinyl alcohol copolymer (EVAL) and carboxylated multi-walled carbon nanotubes (O-MWCNT), and its structural properties were characterized. The improvement of the rheological properties of the waxy oil system by the novel pour point depressant was investigated using macroscopic rheological measurements and microscopic observations. The results showed that EVAL-CNT nanocomposite pour point depressant (PPD) could significantly reduce the pour point and improve the low temperature fluidity of crude oil and had better performance than EVAL-GO at the same addition level. The best effect was achieved at the dosing concentration of 400 ppm, which reduced the pour point by 13 ℃ and the low-temperature viscosity by 85.4%. The nanocomposites dispersed in the oil phase influenced the precipitation and crystallization of wax molecules through heterogeneous crystallization templates, which led to the increase of wax crystal size and compact structure and changed the wax crystal morphology, which had a better effect on the rheological properties of waxy oil.
文摘Oxidative desulfurization from fuel oil is one of the important methods for deep desulfurization.The development of efficient oxidative desulfurization catalysts is crucial for improving the desulfurization performance.Successful encapsulation of phosphotungstic acid(HPW)and ionic liquid(BMImBr)inside the mesoporous cages of MIL-101(Cr)was accomplished through a combination of“bottle around ship”and“ship in bottle”methods.The obtained BMImPW@MIL-101(Cr)composite was characterized by XRD,FTIR,BET,SEM,XPS and ICP methods.Results indicated that the BMImPW@MIL-101(Cr)composites with PW^(3−) loading of 23.1–50.7 wt%were obtained,demonstrating that the“bottle around ship”method is beneficial to make full use of nanocages of MIL-101(Cr)to obtain expected high loading of active PW^(3−) .The BMImPW@MIL-101(Cr)exhibits excellent reusability with no evidence of leaching of active PW^(3−) and BMIm^(+),and well-preserved structure after successive cycles of regeneration and reuse.The significantly improved stability of BMImPW@MIL-101(Cr)as compared to HPW@MIL-101(Cr)is possibly because the leaching of the active PW^(3−) −sites can be greatly suppressed by forming large size of BMImPW owing to introduction of BMIm^(+)cation.The BMImPW@MIL-101(Cr)exhibited excellent catalytic activity for solvent free oxidative desulfurization of refractory sulfides.The enhanced oxidative desulfurization activity as compared to HPW@MIL-101(Cr)can be explained by the intimate contact of sulfides with active PW^(3−) sites owing the strong attraction of BMIm^(+)cation with the sulfides.
基金supported by the Natural Science Foundation of Heilongjiang Province of China (Grant No. LH2019B025)
文摘An efficient extraction-free oxidative desulfurization(ODS)process using a series of cross-linked polyionic liquid phosphotungstate(CLPIL-PW)catalysts is reported.The cross-linked PILs were prepared with DVB and 1-n-alkyl-3-vinyl imidazole hydrobromide(alkyl=ethyl,butyl,octyl,dodecyl),and were then assembled with phosphotungstic acid(H_(3)PW_(12)O_(40))to form the catalysts.The CLPIL-PWs have been applied to the oxidative removal of dibenzothiophene(DBT)from model oil with H_(2)O_(2) as an oxidant.The effects of ionic liquid(IL)cationic species,varying the DVB/IL molar ratio in the polymerization process,and varying operating conditions were investigated.The CLPIL-PWs were characterized by inductively coupled plasma(ICP)mass spectrometry,elemental analysis,scanning electron microscopy(SEM),Fourier transform infra-red(FTIR)spectroscopy,X-ray diffraction(XRD),^(13)C and^(31)P nuclear magnetic resonance(NMR)spectroscopy.The polydivinylbenzene-co-1-n-octyl-3-vinyl imidazole phosphotungstate(P(DVB-OVIm)PW)exhibited the highest DBT removal efficiency(99.9%)and remarkable recyclability,and could be reused eight times without reducing its activity.Finally,an extraction-free ODS mechanism is proposed.
文摘The development of non-noble metal oxidation reduction catalysts(ORR)to improve microbial fuel cell(MFC)performance remains extremely challenging.Herein,the nitrogen-doped iron-based porous carbon nanotube Fe/N@MC-T ORR catalysts were derived from Fe/N-MOF by pyrolyzation using acetonitrile as the nitrogen precursor in a low-cost organic solvent.The Fe/N@MC-T catalysts under different pyrolysis temperatures were characterized by SEM,TEM,BET,XRD,and XPS techniques.Fe/N-MOF showed a smooth rice-like structure with a particle size of about 400×50 nm^(2).The Fe species in Fe/N@MC-T mainly exists in the form of zero-valent iron with a small amount of Fe3C.The results of electrochemical tests revealed that the onset and half-wave potentials of Fe/N@MC-700 were 0.89 V and 0.80 V,respectively,which were only slightly lower than those of the commercial Pt/C(0.92 V and 0.82 V).The MFC with Fe/N@MC-700 showed a highest power density of 864.1 mW/m^(2),which was about 2.25 times that of MFC with carbon cloth,and was slightly lower than that of MFC with Pt/C(20%)(1002.0 mW/m^(2)),which demonstrated that the Fe particles wrapped in carbon nanotubes possessed a relatively high ORR activity.
基金the Northeast Petroleum University Youth Science Foundation (No. 2019QNL-35)Guiding Science and Technology Plan Project of Daqing (No. zd-2021-39)。
文摘The degradation of partially hydrolyzed polyacrylamide(HPAM) found in alkaline/surfactant/polymer flooding sewage was investigated using Fenton-type reagents. Different Fenton reagent treatments for HPAM degradation were compared. The effects of pH, hydrogen peroxide(H_(2)O_(2)), ferrous ion(Fe^(2+)), and tartaric ion(C_(4)H_(4)O_(6)^(2-)) concentrations were studied. The degradation reaction occurred within a wide range of pH(3–9). The HPAM degradation performance of photo-Fenton processes using solar light and UV were compared with that of the Fenton process. The degradation rate was found to be strongly dependent on the H_(2)O_(2)/Fe^(2+)/C_(4)H_(4)O_(6)^(2-)molar ratio. The HPAM degradation efficiency was 90%, and the chemical oxygen demand removal efficiency was 85%. HPAM could be degraded into a compound with a lower molecular weight, but it was difficult to achieve complete mineralization to CO_(2). The presence of intermediate products hindered further oxidation in the Fenton process.
文摘The non-noble metal modified sulfated zirconia was found easy to deactivate.Herein,highly active and highly stable non-noble core-shell Ni-S_(2)O_(8)^(2−)/Al_(2)O_(3)@ZrO_(2) catalysts(Ni-SA@Z-x,x=Al content in wt%)have been successfully prepared and investigated for n-pentane isomerization.The results showed that the core-shell Ni-SA@Z-30 provided a sustained high isopentane yield(63.1%)with little or no deactivation within 5000 min at a mild reaction pressure of 2.0 MPa,which can be attributed to the following factors:(i)carbon deposition was greatly suppressed by the large pore size and huge pore volume;(ii)the loss of sulfur entities was suppressed because the small and highly dispersed tetragonal ZrO_(2) particles can bond with the S species strongly;(iii)strong Brønsted acidity can be maintained well after the isomerization.The pore structures and acid nature of the core-shell Ni-SA@Z-x are entirely different from those of the normal structure Ni-S_(2)O_(8)^(2−)/ZrO_(2)-Al_(2)O_(3),even though the Al content and the compositions of the individual components are the same.The Al_(2)O_(3)cores endow the catalysts with high internal surface area and high mechanical strength.Meanwhile,the ZrO_(2) shell,which consists of more and smaller tetragonal ZrO_(2) particles because of the large surface area of the Al_(2)O_(3)core,promotes the formation of more stable sulfur species and stronger binding sites.
基金Natural Science Foundation of Heilongjiang Province of China(LH2022E030)National Natural Science Foundation of China(21905042).
文摘Heterojunction composites were prepared by silane coupling agent grafting from synthesized graphitic carbon nitride(g-C_(3)N_(4))and commercially available zirconia(ZrO_(2)).The samples were characterized by X-ray diffraction(XRD),scanning electron microscopy(SEM),Fourier transform infrared(FT-IR)spectroscopy,UV-vis diffuse reflectance spectroscopy(DRS),photoluminescence(PL)spectroscopy,and electrochemical impedance spectroscopy(EIS).The photocatalytic activity of the composites was evaluated by the degradation of methylene blue(MB)under visible light irradiation.The results showed that heterojunction composites of g-C_(3)N_(4) and ZrO_(2) could be successfully prepared by coupling agent grafting.The optimal mass ratio of g-C_(3)N_(4) and ZrO_(2) was 2:1,with an activity that was 3.8 times higher than g-C_(3)N_(4) and 15.3 times higher than ZrO_(2).This was ascribed to the stronger light absorption,faster interfacial charge transfer,and lower photogenerated carrier recombination of the heterojunction composites.
基金supported by the National Natural Science Foundation of China (22008134)
文摘Nickel phosphide-carbon-doped alumina(Ni_(2)P/Al_(2)O_(3)-C)catalysts with 10 wt.%Ni_(2)P loading were successfully prepared via a hydrothermal reduction process and the effect of reduction temperature on the hydrodesulfurization(HDS)performance of the as-prepared Ni_(2)P/Al_(2)O_(3)-C catalysts was investigated.The properties of the support(Al_(2)O_(3)-C)and Ni_(2)P/Al_(2)O_(3)-C catalysts were characterized by transmission electron microscopy,scanning electron microscopy,Brunauer-Emmett-Teller measurements,X-ray diffractometry,and X-ray photoelectron spectroscopy.The results indicated that the incorporation of carbon in the support aided the reduction of Ni_(2)P.With an increase in the reduction temperature,Ni and Ni_(12)P_(5) were first generated and then converted into crystalline Ni_(2)P.Furthermore,a higher reduction temperature enhanced the HDS performance of the catalyst by generating more well-dispersed active-phase crystalline Ni_(2)P.
