Since former president Obama of America put forward the concept of 3D printing or additive manufacturing, it had been putting into use rapidly and getting acceptance widely. In particular, metal additive manufacturing...Since former president Obama of America put forward the concept of 3D printing or additive manufacturing, it had been putting into use rapidly and getting acceptance widely. In particular, metal additive manufacturing machines had been successfully applied with pilot demonstration in industry. However, the present metal additive manufacturing machines cannot be directly used in medical fields such as dental restoration because of some different requirements between industry and medical fields. In this case, this paper is aimed for the development of laser fusion printing machine (LFP), also being called as selective laser melting (SLM), for ceramic teeth crown in dental restoration business. Through the reasonable design and development of key components such as machinery unit, optical unit, electrical controlling unit, and software unit, and the integration, debugging, and optimization of the entire system, the laser fusion printing apparatus for dental restoration has been successfully developed. Key technologies such as machine structure design, optical unit design, electrical controlling system design, system software and process software have been overcome, on the basis of which, a lot of process experiments of medical titanium alloy materials were deeply carried out. At last laser fusion printing technology of titanium alloy was mastered, and titanium dental crown by laser fusion printing with relative density up to 97.37% was realized. After post treatment with porcelain, it was found that the laser fusion printed porcelain teeth with titanium alloy has good metal-ceramic bonding strength, which is equivalent to the quality of traditional porcelain teeth, which showed that laser fusion printing can meet the requirements of dental restoration business and has a broad market outlook.展开更多
Objective:Flavonoids are the bioactive compounds in safflower(Carthamus tinctorius),in which chalcone synthase(CHS)is the first limiting enzyme.However,it is unclear that which chalcone synthase genes(CHSs)are partici...Objective:Flavonoids are the bioactive compounds in safflower(Carthamus tinctorius),in which chalcone synthase(CHS)is the first limiting enzyme.However,it is unclear that which chalcone synthase genes(CHSs)are participated in flavonoids biosynthesis in C.tinctorius.In this study,the CHSs in the molecular characterization and enzyme activities were investigated.Methods:Putative chalcone biosynthase genes were screened by the full-length transcriptome sequences data in C.tinctorius.Chalcone biosynthase genes in C.tinctorius(CtCHSs)were cloned from cDNA of flowers of C.tinctorius.The cloned gene sequences were analyzed by bioinformatics,and their expression patterns were analyzed by real-time PCR(RT-PCR).The protein of CtCHS in the development of flowers was detected by polyclonal antibody Western blot.A recombinant vector of CtCHS was constructed.The CtCHS recombinant protein was induced and purified to detect the enzyme reaction(catalyzing the reaction of p-coumaryl-CoA and malonyl-CoA to produce naringin chalcone).The reaction product was detected by HPLC and LC-MS.Results:Two full-length CtCHS genes were successfully cloned from the flowers of safflower(CtCHS1 and CtCHS3),with gene lengths of 1525 bp and 1358 bp,respectively.RT-PCR analysis showed that both genes were highly expressed in the flowers,but the expression of CtCHS1 was higher than that of CtCHS3 at each developmental stage of the flowers.WB analysis showed that only CtCHS1 protein could be detected at each developmental stage of the flowers.HPLC and LC-MS analyses showed that CtCHS1 could catalyze the conversion of p-coumaryl-CoA and malonyl-CoA substrates to naringin chalcone.Conclusion:CtCHS1 is involved in the biosynthesis of naringin chalcone in safflower.展开更多
Aqueous zinc battery has been regarded as one of the most promising energy storage systems due to its low cost and environmental benignity.However,the safety concern on Zn anodes caused by uncontrolled Zn dendrite gro...Aqueous zinc battery has been regarded as one of the most promising energy storage systems due to its low cost and environmental benignity.However,the safety concern on Zn anodes caused by uncontrolled Zn dendrite growth in aqueous electrolyte hinders their application.Herein,sucrose with multi-hydroxyl groups has been introduced into aqueous electrolyte to modify Zn^(2+)solvation environment and create a protection layer on Zn anode,thus effectively retarding the growth of zinc dendrites.Atomistic simulations and experiments confirm that sucrose molecules can enter into the solvation sheath of Zn^(2+),and the as-formed unique solvation structure enhances the mobility of Zn^(2+).Such fast Zn^(2+)kinetics in sucrose-modified electrolyte can successfully suppress the dendrite growth.With this sucrose-modified aqueous electrolyte,Zn/Zn symmetric cells present more stable cycle performance than those using pure aqueous electrolyte;Zn/C cells also deliver an impressive higher energy density of 129.7 Wh·kg^(−1)and improved stability,suggesting a great potential application of sucrose-modified electrolytes for future Zn batteries.展开更多
光纤复合架空地线(OPGW)故障频发的原因与光缆局部受到的应力有直接关系,为了实现对OPGW光缆的在线应变监测,搭建了长距离布里渊光时域分析(BOTDA)和布里渊光时域反射(BOTDR)系统,并对重覆冰区域运行年限超过15年的在运95.14 km OPGW进...光纤复合架空地线(OPGW)故障频发的原因与光缆局部受到的应力有直接关系,为了实现对OPGW光缆的在线应变监测,搭建了长距离布里渊光时域分析(BOTDA)和布里渊光时域反射(BOTDR)系统,并对重覆冰区域运行年限超过15年的在运95.14 km OPGW进行了应变检测和分析。通过对同一段光缆的对比测量,结果表明:BOTDA系统具有更长的测量距离、更高的空间分辨率与更高的测量精度,能准确辨别引下线并识别零应变参考点,可以实现温度和应变信息的准确分离。在两个站点的距离超过BOTDA系统的测量量程时,可以使用BOTDR系统从光缆两端分别测量以覆盖全部光缆。同时,BOTDR系统展现出单端测量的优势,在断纤故障发生时,BOTDR系统可不影响断点之前的线路测量。在同一条OPGW光缆线路上通过多维度的对比,分析了两种技术在OPGW光缆监测中的优劣势,为分布式光纤传感技术在电力系统中的应用提供参考。展开更多
Organic solid-state luminescent materials with high-efficiency deep-red emission have attracted considerable interest in recent years.Constructing donor-acceptor(D-A)type molecules has been one of most commonly used s...Organic solid-state luminescent materials with high-efficiency deep-red emission have attracted considerable interest in recent years.Constructing donor-acceptor(D-A)type molecules has been one of most commonly used strategies to achieve deep-red emission,but it is always difficult to achieve high photoluminescence(PL)quantum yield(ηPL)due to forbidden charge-transfer state.Herein,we report a new D-A type molecule 4-(7-(4-(diphenylamino)phenyl)-9-oxo-9H-fluoren-2-yl)benzonitrile(TPAFOCN),deriving from donor-acceptor-donor(D-A-D)type 2,7-bis(4-(diphenylamino)phenyl)-9H-fluoren-9-one(DTPA-FO)with a fluorescence maximum of 627 nm in solids.This molecular design enables a transformation of acceptor from fluorenone(FO)itself to 4-(9-oxo-9H-fluoren-2-yl)benzonitrile(FOCN).Compared with DTPA-FO,the introduction of cyanophenyl not only shifts the emission of TPA-FOCN to deep red with a fluorescence maximum of 668 nm in solids,but also maintains the highηPL of 10%.Additionally,a solution-processed non-doped organic light-emitting diode(OLED)was fabricated with TPA-FOCN as emitter.TPA-FOCN device showed a maximum luminous efficiency of 0.13 cd/A and a maximum external quantum efficiency(EQE)of 0.22%with CIE coordinates of(0.64,0.35).This work provides a valuable strategy for the rational design of high-efficiency deep-red emission materials using cyanophenyl as an ancillary acceptor.展开更多
Covalent organic frameworks(COFs)characterized by structural diversity,face-to-face stacking and open channels exhibit unique advantages as photothermal materials but have rarely been applied in solar-driven water eva...Covalent organic frameworks(COFs)characterized by structural diversity,face-to-face stacking and open channels exhibit unique advantages as photothermal materials but have rarely been applied in solar-driven water evaporation due to complicated framework design,tedious synthesis,and low solar-to-vapor efficiency.Herein,we report a materials design strategy to produce efficient and robust photothermal COF by anchoring nonemissive radicals to the pore surface by a[2+2]cycloaddition–retroelectrocyclization reaction.展开更多
文摘Since former president Obama of America put forward the concept of 3D printing or additive manufacturing, it had been putting into use rapidly and getting acceptance widely. In particular, metal additive manufacturing machines had been successfully applied with pilot demonstration in industry. However, the present metal additive manufacturing machines cannot be directly used in medical fields such as dental restoration because of some different requirements between industry and medical fields. In this case, this paper is aimed for the development of laser fusion printing machine (LFP), also being called as selective laser melting (SLM), for ceramic teeth crown in dental restoration business. Through the reasonable design and development of key components such as machinery unit, optical unit, electrical controlling unit, and software unit, and the integration, debugging, and optimization of the entire system, the laser fusion printing apparatus for dental restoration has been successfully developed. Key technologies such as machine structure design, optical unit design, electrical controlling system design, system software and process software have been overcome, on the basis of which, a lot of process experiments of medical titanium alloy materials were deeply carried out. At last laser fusion printing technology of titanium alloy was mastered, and titanium dental crown by laser fusion printing with relative density up to 97.37% was realized. After post treatment with porcelain, it was found that the laser fusion printed porcelain teeth with titanium alloy has good metal-ceramic bonding strength, which is equivalent to the quality of traditional porcelain teeth, which showed that laser fusion printing can meet the requirements of dental restoration business and has a broad market outlook.
基金supported by grants from the National Natural Science Foundation of China(No.82274039,81803669)China Postdoctoral Science Foundation(No.2018M643790XB)。
文摘Objective:Flavonoids are the bioactive compounds in safflower(Carthamus tinctorius),in which chalcone synthase(CHS)is the first limiting enzyme.However,it is unclear that which chalcone synthase genes(CHSs)are participated in flavonoids biosynthesis in C.tinctorius.In this study,the CHSs in the molecular characterization and enzyme activities were investigated.Methods:Putative chalcone biosynthase genes were screened by the full-length transcriptome sequences data in C.tinctorius.Chalcone biosynthase genes in C.tinctorius(CtCHSs)were cloned from cDNA of flowers of C.tinctorius.The cloned gene sequences were analyzed by bioinformatics,and their expression patterns were analyzed by real-time PCR(RT-PCR).The protein of CtCHS in the development of flowers was detected by polyclonal antibody Western blot.A recombinant vector of CtCHS was constructed.The CtCHS recombinant protein was induced and purified to detect the enzyme reaction(catalyzing the reaction of p-coumaryl-CoA and malonyl-CoA to produce naringin chalcone).The reaction product was detected by HPLC and LC-MS.Results:Two full-length CtCHS genes were successfully cloned from the flowers of safflower(CtCHS1 and CtCHS3),with gene lengths of 1525 bp and 1358 bp,respectively.RT-PCR analysis showed that both genes were highly expressed in the flowers,but the expression of CtCHS1 was higher than that of CtCHS3 at each developmental stage of the flowers.WB analysis showed that only CtCHS1 protein could be detected at each developmental stage of the flowers.HPLC and LC-MS analyses showed that CtCHS1 could catalyze the conversion of p-coumaryl-CoA and malonyl-CoA substrates to naringin chalcone.Conclusion:CtCHS1 is involved in the biosynthesis of naringin chalcone in safflower.
基金support from the National Natural Science Foundation of China(Nos.22075313 and 21975281)the National Key Research and Development Program of China(No.2020YFB1312902)+3 种基金the Science and Technology Project of Jiangxi Province(No.20192BCD40017)Outstanding Youth Fund of Jiangxi Province(No.20192BCB23028)Jiangxi Double Thousand Talent Program(No.JXSQ2019101072)Science Technology Major Project of Nanchang(No.2020BI47)is acknowledged.
文摘Aqueous zinc battery has been regarded as one of the most promising energy storage systems due to its low cost and environmental benignity.However,the safety concern on Zn anodes caused by uncontrolled Zn dendrite growth in aqueous electrolyte hinders their application.Herein,sucrose with multi-hydroxyl groups has been introduced into aqueous electrolyte to modify Zn^(2+)solvation environment and create a protection layer on Zn anode,thus effectively retarding the growth of zinc dendrites.Atomistic simulations and experiments confirm that sucrose molecules can enter into the solvation sheath of Zn^(2+),and the as-formed unique solvation structure enhances the mobility of Zn^(2+).Such fast Zn^(2+)kinetics in sucrose-modified electrolyte can successfully suppress the dendrite growth.With this sucrose-modified aqueous electrolyte,Zn/Zn symmetric cells present more stable cycle performance than those using pure aqueous electrolyte;Zn/C cells also deliver an impressive higher energy density of 129.7 Wh·kg^(−1)and improved stability,suggesting a great potential application of sucrose-modified electrolytes for future Zn batteries.
文摘光纤复合架空地线(OPGW)故障频发的原因与光缆局部受到的应力有直接关系,为了实现对OPGW光缆的在线应变监测,搭建了长距离布里渊光时域分析(BOTDA)和布里渊光时域反射(BOTDR)系统,并对重覆冰区域运行年限超过15年的在运95.14 km OPGW进行了应变检测和分析。通过对同一段光缆的对比测量,结果表明:BOTDA系统具有更长的测量距离、更高的空间分辨率与更高的测量精度,能准确辨别引下线并识别零应变参考点,可以实现温度和应变信息的准确分离。在两个站点的距离超过BOTDA系统的测量量程时,可以使用BOTDR系统从光缆两端分别测量以覆盖全部光缆。同时,BOTDR系统展现出单端测量的优势,在断纤故障发生时,BOTDR系统可不影响断点之前的线路测量。在同一条OPGW光缆线路上通过多维度的对比,分析了两种技术在OPGW光缆监测中的优劣势,为分布式光纤传感技术在电力系统中的应用提供参考。
基金supported by the National Natural Science Foundation of China(Nos.91833304,51873077,51803071 and51673083)the National Basic Research Program of China(Nos.2015CB655003 and 2016YFB0401001)+2 种基金the Postdoctoral Innovation Talent Support Project(Nos.BX201700097 and BX20180121)the China Postdoctoral Science Foundation(Nos.2017M620108 and2018M641767)JLUSTIRT(No.2019TD-33)
文摘Organic solid-state luminescent materials with high-efficiency deep-red emission have attracted considerable interest in recent years.Constructing donor-acceptor(D-A)type molecules has been one of most commonly used strategies to achieve deep-red emission,but it is always difficult to achieve high photoluminescence(PL)quantum yield(ηPL)due to forbidden charge-transfer state.Herein,we report a new D-A type molecule 4-(7-(4-(diphenylamino)phenyl)-9-oxo-9H-fluoren-2-yl)benzonitrile(TPAFOCN),deriving from donor-acceptor-donor(D-A-D)type 2,7-bis(4-(diphenylamino)phenyl)-9H-fluoren-9-one(DTPA-FO)with a fluorescence maximum of 627 nm in solids.This molecular design enables a transformation of acceptor from fluorenone(FO)itself to 4-(9-oxo-9H-fluoren-2-yl)benzonitrile(FOCN).Compared with DTPA-FO,the introduction of cyanophenyl not only shifts the emission of TPA-FOCN to deep red with a fluorescence maximum of 668 nm in solids,but also maintains the highηPL of 10%.Additionally,a solution-processed non-doped organic light-emitting diode(OLED)was fabricated with TPA-FOCN as emitter.TPA-FOCN device showed a maximum luminous efficiency of 0.13 cd/A and a maximum external quantum efficiency(EQE)of 0.22%with CIE coordinates of(0.64,0.35).This work provides a valuable strategy for the rational design of high-efficiency deep-red emission materials using cyanophenyl as an ancillary acceptor.
基金supported by the National Natural Science Foundation of China(grant nos.21975078 and 51973063)the Guangdong Basic and Applied Basic Research Foundation(no.2021A1515010311)+1 种基金the Natural Science Foundation of Guangdong Province(no.2019B030301003)the 111 Project,and the Thousand Talents Plan.C.Gu and Y.Su acknowledge the scholarship support from the China Scholarship Council(grant nos.202006155049 and 202006150059).Q.X.acknowledges the financial support from the Shanghai Pujiang Program(no.19PJ1410400)and the Natural Science Foundation of Shanghai(no.20ZR1464000).Z.C.and Y.L.acknowledge the financial support of the Tip-top Scientific and Technical Innovative Youth Talents of Guangdong Special Support Program(no.2019TQ05C890),and the Pearl River S&T Nova Program of Guangzhou(no.201710010194).
文摘Covalent organic frameworks(COFs)characterized by structural diversity,face-to-face stacking and open channels exhibit unique advantages as photothermal materials but have rarely been applied in solar-driven water evaporation due to complicated framework design,tedious synthesis,and low solar-to-vapor efficiency.Herein,we report a materials design strategy to produce efficient and robust photothermal COF by anchoring nonemissive radicals to the pore surface by a[2+2]cycloaddition–retroelectrocyclization reaction.