The liquid-solid compound casting technology was used to produce the AZ91D/0Cr19Ni9 bimetal composite without and with hot dipping aluminium, respectively. The influences of Al coating on microstructures and mechanica...The liquid-solid compound casting technology was used to produce the AZ91D/0Cr19Ni9 bimetal composite without and with hot dipping aluminium, respectively. The influences of Al coating on microstructures and mechanical properties of AZ91D/0Cr19Ni9 interface were investigated. The results showed that the mechanical bonding was obtained between AZ91D and bare steel 0Cr19Ni9 where a gap existed at the interface; the metallurgical bonding was formed between AZ91D and Al-coated 0Cr19Ni9, which could be divided into two different intermetallic layers: layer Ⅰ was mainly composed of α-Mg+β-Mg17Al12 eutectic structure and a small amount of MgAl2O4, and layer Ⅱ mainly comprised of Fe2Al5 intermetallic compound. Furthermore, the hardness value of interface was obviously higher than that of AZ91D matrix, and the average hardness values of layers Ⅰ and Ⅱ were HV 158 and HV 493, respectively. The shear strength of AZ91D/Al-coated 0Cr19Ni9 interface was higher than that of AZ91D/bare 0Cr19Ni9 interface, which confirmed that Al coating could improve the adhesive strength between AZ91D and 0Cr19Ni9 during liquid-solid compound casting process.展开更多
Devising exceptional S-scheme heterojunction photocatalysts utilized in annihilating pharmaceuticals and chromium contamination is significant for addressing the problem of global water pollution.In this work,a chemic...Devising exceptional S-scheme heterojunction photocatalysts utilized in annihilating pharmaceuticals and chromium contamination is significant for addressing the problem of global water pollution.In this work,a chemically bonded Mn0.5Cd_(0.5)S/BiOBr S-scheme heterostructure with oxygen vacancies is ingeniously developed through a facile in-situ solvothermal synthesis.The designed Mn0.5Cd_(0.5)S/BiOBr heterojunction exhibits eminently reinforced photo-activity for destruction of tetracycline hydrochloride and Cr(VI)as compared with its individual components.This substantial photo-redox performance amelioration is benefitted from the creation of an intense internal electric field(IEF)via supplying powerful driving force and migration highway by interfacial chemical bond to foster the S-scheme electron/hole disintegration.More intriguingly,the IEF at the hetero-interface drives the fast consumption of the photo-induced holes in Mn0.5Cd_(0.5)S by the photoelectrons from BiOBr,profoundly boosting the enrichment of active photo-carriers and sparing the photo-corrosion of Mn0.5Cd_(0.5)S.Furthermore,Mn0.5Cd_(0.5)S/BiOBr with exceptional anti-interference property can work efficiently in real water matrices.Multiple uses of the recycled Mn0⋅5Cd0⋅5S/BiOBr evidence its prominent robustness and stability.This achievement indicates the vast potential of chemically bonded S-scheme photosystems with structural defects in the design of photo-responsive materials for effective wastewater treatment.展开更多
Current bio-ethanol production entails the enzymatic depolymerization of cellulose,but this process shows low efficiency and poor economy.In this work,we developed a consecutive aqueous hydrogenolysis process for the ...Current bio-ethanol production entails the enzymatic depolymerization of cellulose,but this process shows low efficiency and poor economy.In this work,we developed a consecutive aqueous hydrogenolysis process for the conversion of corn-stalk cellulose to produce a relatively high concentration of bio-ethanol(6.1 wt%)without humin formation.A high yield of cellulose(ca.50 wt%)is extracted from corn stalk using a green solvent(80 wt%1,4-butanediol)without destroying the structure of the lignin.The first hydrothermal hydrogenolysis step uses a Ni–WO_(x)/SiO_(2)catalyst to convert the high cumulative concentration of cellulose(30 wt%)into a polyol mixture with a 56.5 C%yield of ethylene glycol(EG).The original polyol mixture is then subjected to subsequent selective aqueous-phase hydrogenolysis of the C–O bond to produce bioethanol(75%conversion,84 C%selectivity)over the modified hydrothermally stable Cu catalysts.The added Ni component favors the good dispersion of Cu nanoparticles,and the incorporated Au3+helps to stabilize the active Cu^(0)-Cu^(+)species.This multi-functional catalytic process provides an economically competitive route for the production of cellulosic ethanol from raw lignocellulose.展开更多
Ce （III） Y zeolite was prepared by liquid-phase ion-exchange of NaY with 0.1 mol/L Ce（NO3）3 solution at 100℃ for 4 h. After calcining the resultant Ce （III） Y zeolite at 550 ℃ in air, Ce （IV） Y zeolite was o...Ce （III） Y zeolite was prepared by liquid-phase ion-exchange of NaY with 0.1 mol/L Ce（NO3）3 solution at 100℃ for 4 h. After calcining the resultant Ce （III） Y zeolite at 550 ℃ in air, Ce （IV） Y zeolite was obtained. Desulfurization of FCC gasoline was studied by selective adsorption with Ce （IV） Y zeolite. The results showed that Ce （IV） Y zeolite can remove thiophene via 0-complexation directly, while thiophene and Ce （IV） can form stable chemical bonds （sulfur-metal bonds） that can enhance the capability of Ce （IV） Y zeolite for adsorption of thiophene.展开更多
A novel sextuple hydrogen-bonding （HB） self-assembly molecular heterodimer bearing an iridium complex as the indicator dye and two carbazoles as the reference dye, namely 6HB-Irbt-Cz, was synthesized, and its molecu...A novel sextuple hydrogen-bonding （HB） self-assembly molecular heterodimer bearing an iridium complex as the indicator dye and two carbazoles as the reference dye, namely 6HB-Irbt-Cz, was synthesized, and its molecular structure was confirmed by ^1H NMR, ^13CNMR, TOF-MS and 2D NMR. Because of the inefficient energy transfer process between the carbazole and iridium complex units, 6HB-Irbt-Cz exhibits distinct fluorescence/ phosphorescence dual emission in neat film state. More importantly, the neat film sample of 6HB-Irbt-Cz could display linear ratiometric optical response toward oxygen in the full oxygen concentration range from 0 to 100 vol%, together with good stability, reversibility and rapid response-recovery times. Note that this represents the first discovery of neat-film-based oxygen sensor capable of showing strictly linear ratiometric Stem-Volmer behavior in the oxygen concentration of 0- 100 vol%.展开更多
基金Project(cstc2015yykfC0001)supported by the National Engineering Research Centre for Magnesium Alloys,ChinaProject supported by State Key Laboratory of Mechanical Transmission of Chongqing University,China
文摘The liquid-solid compound casting technology was used to produce the AZ91D/0Cr19Ni9 bimetal composite without and with hot dipping aluminium, respectively. The influences of Al coating on microstructures and mechanical properties of AZ91D/0Cr19Ni9 interface were investigated. The results showed that the mechanical bonding was obtained between AZ91D and bare steel 0Cr19Ni9 where a gap existed at the interface; the metallurgical bonding was formed between AZ91D and Al-coated 0Cr19Ni9, which could be divided into two different intermetallic layers: layer Ⅰ was mainly composed of α-Mg+β-Mg17Al12 eutectic structure and a small amount of MgAl2O4, and layer Ⅱ mainly comprised of Fe2Al5 intermetallic compound. Furthermore, the hardness value of interface was obviously higher than that of AZ91D matrix, and the average hardness values of layers Ⅰ and Ⅱ were HV 158 and HV 493, respectively. The shear strength of AZ91D/Al-coated 0Cr19Ni9 interface was higher than that of AZ91D/bare 0Cr19Ni9 interface, which confirmed that Al coating could improve the adhesive strength between AZ91D and 0Cr19Ni9 during liquid-solid compound casting process.
基金supported by the National Natural Science Foundation of China(U1809214)the Natural Science Foundation of Zhejiang Province(LY20E080014 and LTGN23E080001)the Science and Technology Project of Zhoushan(2022C41011).
文摘Devising exceptional S-scheme heterojunction photocatalysts utilized in annihilating pharmaceuticals and chromium contamination is significant for addressing the problem of global water pollution.In this work,a chemically bonded Mn0.5Cd_(0.5)S/BiOBr S-scheme heterostructure with oxygen vacancies is ingeniously developed through a facile in-situ solvothermal synthesis.The designed Mn0.5Cd_(0.5)S/BiOBr heterojunction exhibits eminently reinforced photo-activity for destruction of tetracycline hydrochloride and Cr(VI)as compared with its individual components.This substantial photo-redox performance amelioration is benefitted from the creation of an intense internal electric field(IEF)via supplying powerful driving force and migration highway by interfacial chemical bond to foster the S-scheme electron/hole disintegration.More intriguingly,the IEF at the hetero-interface drives the fast consumption of the photo-induced holes in Mn0.5Cd_(0.5)S by the photoelectrons from BiOBr,profoundly boosting the enrichment of active photo-carriers and sparing the photo-corrosion of Mn0.5Cd_(0.5)S.Furthermore,Mn0.5Cd_(0.5)S/BiOBr with exceptional anti-interference property can work efficiently in real water matrices.Multiple uses of the recycled Mn0⋅5Cd0⋅5S/BiOBr evidence its prominent robustness and stability.This achievement indicates the vast potential of chemically bonded S-scheme photosystems with structural defects in the design of photo-responsive materials for effective wastewater treatment.
文摘Current bio-ethanol production entails the enzymatic depolymerization of cellulose,but this process shows low efficiency and poor economy.In this work,we developed a consecutive aqueous hydrogenolysis process for the conversion of corn-stalk cellulose to produce a relatively high concentration of bio-ethanol(6.1 wt%)without humin formation.A high yield of cellulose(ca.50 wt%)is extracted from corn stalk using a green solvent(80 wt%1,4-butanediol)without destroying the structure of the lignin.The first hydrothermal hydrogenolysis step uses a Ni–WO_(x)/SiO_(2)catalyst to convert the high cumulative concentration of cellulose(30 wt%)into a polyol mixture with a 56.5 C%yield of ethylene glycol(EG).The original polyol mixture is then subjected to subsequent selective aqueous-phase hydrogenolysis of the C–O bond to produce bioethanol(75%conversion,84 C%selectivity)over the modified hydrothermally stable Cu catalysts.The added Ni component favors the good dispersion of Cu nanoparticles,and the incorporated Au3+helps to stabilize the active Cu^(0)-Cu^(+)species.This multi-functional catalytic process provides an economically competitive route for the production of cellulosic ethanol from raw lignocellulose.
文摘Ce （III） Y zeolite was prepared by liquid-phase ion-exchange of NaY with 0.1 mol/L Ce（NO3）3 solution at 100℃ for 4 h. After calcining the resultant Ce （III） Y zeolite at 550 ℃ in air, Ce （IV） Y zeolite was obtained. Desulfurization of FCC gasoline was studied by selective adsorption with Ce （IV） Y zeolite. The results showed that Ce （IV） Y zeolite can remove thiophene via 0-complexation directly, while thiophene and Ce （IV） can form stable chemical bonds （sulfur-metal bonds） that can enhance the capability of Ce （IV） Y zeolite for adsorption of thiophene.
基金We acknowledge the financial support for this work by the National Natural Science Foundation of China （No. 21372168）.
文摘A novel sextuple hydrogen-bonding （HB） self-assembly molecular heterodimer bearing an iridium complex as the indicator dye and two carbazoles as the reference dye, namely 6HB-Irbt-Cz, was synthesized, and its molecular structure was confirmed by ^1H NMR, ^13CNMR, TOF-MS and 2D NMR. Because of the inefficient energy transfer process between the carbazole and iridium complex units, 6HB-Irbt-Cz exhibits distinct fluorescence/ phosphorescence dual emission in neat film state. More importantly, the neat film sample of 6HB-Irbt-Cz could display linear ratiometric optical response toward oxygen in the full oxygen concentration range from 0 to 100 vol%, together with good stability, reversibility and rapid response-recovery times. Note that this represents the first discovery of neat-film-based oxygen sensor capable of showing strictly linear ratiometric Stem-Volmer behavior in the oxygen concentration of 0- 100 vol%.
