Paraphenylenediamine(PPDA)-grafted maleic anhydride(MAH)-modified graphene oxide(PGO)was synthesized through a dual modification process.Initially,MAH was employed to modify graphene oxide(GO)to enhance its reactive s...Paraphenylenediamine(PPDA)-grafted maleic anhydride(MAH)-modified graphene oxide(PGO)was synthesized through a dual modification process.Initially,MAH was employed to modify graphene oxide(GO)to enhance its reactive sites.Subsequently,PPDA was utilized for further modification of MAH-modified GO(MGO).Through a comprehensive analysis,the successful grafting of MAH and PPDA onto GO was confirmed.It was concurrently established that the optimal ratio of PPDA to MGO is 1:1.This approach yielded PGO characterized by outstanding dispersibility and barrier properties in epoxy resin(EP)coaings for Q235 steel.The corrosion resistance of EP coatings containing varying amounts of PGO was assessed using electrochemical workstation and salt spray testing.After immersing in a 3.5 wt.%NaCl solution for 300 h,the composite coating containing 0.1 wt.%PGO exhibited superior performance in terms of low-frequency impedance modulus,measuring at 1.1×10^(8)Ωcm^(2).The lowest corrosion current density was 2.32×10^(–10)A cm^(−2),and the self-corrosion voltage was−0.301 V.Additionally,polarization testing indicated that this coating also displayed the lowest corrosion rate,specifically 1.383×10^(–7)mm/a.展开更多
Chemical modification of polymers represents a pivotal method for achieving functionalized polymer materials.However,due to the lack of post-functional handle,the chemical modification of polyester materials remains a...Chemical modification of polymers represents a pivotal method for achieving functionalized polymer materials.However,due to the lack of post-functional handle,the chemical modification of polyester materials remains a significant challenge.Ring-opening copolymerization of cyclic anhydride and epoxides is a powerful approach to synthesize polyesters.In this work,we for the first time demonstrate the functionalizability of polyesters synthesized with brominated anhydride monomers.The post-functionalization is amenable to a wide variety of reactive groups and reactions with high yields.With multiple well-established functionalization pathways of brominated polyester materials and optimized the conditions for the modification reactions,a series of functionalized polyester materials can be obtained with high yields,providing new insights for the research about functionalization of polymers.展开更多
Bacterial resistance and excessive inflammation are common issues that hinder wound healing.Antimicrobial peptides(AMPs)offer a promising and versatile antibacterial option compared to traditional antibiotics,with add...Bacterial resistance and excessive inflammation are common issues that hinder wound healing.Antimicrobial peptides(AMPs)offer a promising and versatile antibacterial option compared to traditional antibiotics,with additional anti-inflammatory properties.However,the applications of AMPs are limited by their antimicrobial effects and stability against bacterial degradation.TFNAs are regarded as a promising drug delivery platform that could enhance the antibacterial properties and stability of nanodrugs.Therefore,in this study,a composite hydrogel(HAMA/t-GL13K)was prepared via the photocross-linking method,in which tFNAs carry GL13K.The hydrogel was injectable,biocompatible,and could be instantly photocured.It exhibited broad-spectrum antibacterial and anti-inflammatory properties by inhibiting the expression of inflammatory factors and scavenging ROS.Thereby,the hydrogel inhibited bacterial infection,shortened the wound healing time of skin defects in infected skin full-thickness defect wound models and reduced scarring.The constructed HAMA/tFNA-AMPs hydrogels exhibit the potential for clinical use in treating microbial infections and promoting wound healing.展开更多
Ni/Al2O3 catalysts were derived from spinel NiAl2O4 with different Ni content ((2.5, 5 and 7.5) wt%). The catalysts were obtained by H-2 reduction and were investigated for the low-temperature hydrogenation of maleic ...Ni/Al2O3 catalysts were derived from spinel NiAl2O4 with different Ni content ((2.5, 5 and 7.5) wt%). The catalysts were obtained by H-2 reduction and were investigated for the low-temperature hydrogenation of maleic anhydride (MA) to produce succinic anhydride (SA). The characterization results showed that Ni-0 active sites were mainly derived during the H2 reduction from spinel NiAl2O4 Among the catalysts studied, employing the optimum preparation and reaction conditions with Ni(5%)/Al2O3 yielded the highest catalytic performance. A near-100% conversion of MA and similar to 90% selectivity to SA were achieved at 120 degrees C and 0.5 MPa of H-2 with a weighted hourly space velocity (MA) of 2 h(-1). (C) 2017, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.展开更多
The pseudo-boehmite derived alumina supported metal（Cu,Co and Ni） catalysts prepared by the impregnation method were investigated in hydrogenation of maleic anhydride（MA） to succinic anhydride（SA） and γ-butyrol...The pseudo-boehmite derived alumina supported metal（Cu,Co and Ni） catalysts prepared by the impregnation method were investigated in hydrogenation of maleic anhydride（MA） to succinic anhydride（SA） and γ-butyrolactone.The catalysts were characterized by ICP-AES,N2 adsorptiondesorption,XRD,H2-TPR,CO-TPD,dissociative N2O adsorption and TEM and the results showed that the alumina possessed mesoporous feature and the metal species were well dispersed on the support.Compared to Cu/Al2O3 and Co/Al2O3,Ni/Al2O3 exhibited higher catalytic activity in the MA hydrogenation with 92%selectivity to SA and nearly 100%conversion of MA at 140 °C under 0.5 MPa of H2 with a weighted hourly space velocity of 2 h 1（MA）.The stability of Ni/Al2O3 catalyst was also investigated.展开更多
In this work, the hydrogenation of maleic anhydride to succinic anhydride in the presence of 5 m%Ni/clay catalysts was investigated. These catalysts were characterized by X-ray diffraction （XRD）, H2 temperature prog...In this work, the hydrogenation of maleic anhydride to succinic anhydride in the presence of 5 m%Ni/clay catalysts was investigated. These catalysts were characterized by X-ray diffraction （XRD）, H2 temperature programmed reduction （TPR） and thermogravimetric analysis （TGA） techniques. The XRD and TPR studies showed that Ni was present as Ni2＋ on the support, which indicated that there were no elemental nickel （Ni^0） and Ni203 species in the unreduced samples. Increasing of calcination temperature to 650 ℃ leads to destruction of the support structure observed in TGA, while the catalyst sample calcined at 550 ℃ exhibits better performances than other samples. The ideal conversion of maleic anhydride （97.14%） and selectivity of succinic anhydride （99.55%） were realized at a reaction temperature of 180 ℃ and a weight hourly space velocity of 4 h^-1 under a reaction pressure of 1 MPa.展开更多
The colloidal carbon microspheres(CMS)were prepared by the hydrothermal method.The nickel catalysts supported on carbon microspheres(Ni/CMS)were further prepared and were characterized by the Fourier transform infrare...The colloidal carbon microspheres(CMS)were prepared by the hydrothermal method.The nickel catalysts supported on carbon microspheres(Ni/CMS)were further prepared and were characterized by the Fourier transform infrared spectroscopy(FTIR),the X-ray diffraction(XRD),the scanning electron microscopy(SEM),the transmission electron microscopy(TEM),and the N_(2)adsorption technique.The selective hydrogenation of maleic anhydride(MA)to succinic anhydride(SA)over the Ni/CMS catalysts was investigated.The results indicated that the Ni/CMS catalyst,which was prepared with glucose as carbon source and calcined at 500℃,exhibited the best performance.The hydrogen pressure,reaction temperature,and reaction time could significantly affect the conversion of maleic anhydride during the hydrogenation reaction.A 98.4%conversion of MA and an 100%selectivity to SA were achieved over the Ni/CMS catalyst in acetic anhydride solvent under mild conditions covering a temperature of 90℃,a H2 pressure of 1.0 MPa,and a reaction time of 3 h.展开更多
Fluoroalkyl-containing organic compounds have exhibited wide applications in the field of pharmaceuticals,agrochemicals and materials science due to their outstanding properties such as biological activity,metabolic s...Fluoroalkyl-containing organic compounds have exhibited wide applications in the field of pharmaceuticals,agrochemicals and materials science due to their outstanding properties such as biological activity,metabolic stability,lipophilicity,excellent chemical and thermal stability.Therefore,various synthetic strategies have been developed for the construction of fluoroalkyl-containing compounds,using highly active fluorinating reagents and fluorinated building blocks.Recently,the use of easily available and inexpensive trifluoroacetic anhydride(TFAA)and its anhydride analogues has attracted great attention to access numerous fluoroalkyl-containing compounds through cyclization and coupling reactions.In this review,we summarized the recent advances in the synthesis of fluoroalkylated compounds using fluoroalkyl anhydrides as reagents.This review aims to provide a reference for researchers on how to develop new synthetic straregies of fluorine-containing organic compounds and achieve kilograms or even tons preparation of fluorine-containing organic compounds using fluoroalkyl anhydrides.展开更多
Starch,as a typical polysaccharide with natural spherical morphology,is not only a preferred precursor for preparing carbon materials but also a model polymer for investigating thermochemical evolution mechanisms.Howe...Starch,as a typical polysaccharide with natural spherical morphology,is not only a preferred precursor for preparing carbon materials but also a model polymer for investigating thermochemical evolution mechanisms.However,starch usually suffers from severe foaming and low carbon yield during direct pyrolysis.Herein,we report a simple and eco-friendly dry strategy,by maleic anhydride initiating the esterification of starch,to design carbon microspheres against the starch foaming.Moreover,the infuence of ester grafting on the pyrolytic behavior of starch is also focused.The formation of ester groups in precursor guarantees the structural stability of starch-based intermediate because it can promote the accumulation of unsaturated species and accelerate the water elimination during pyrolysis.Meanwhile,the esterification and dehydration reactions greatly deplete the primary hydroxyl groups in the starch molecules and thus the rapid levoglucosan release is inhibited,which well keeps the spherical morphology of starch and ensures the high carbon yield.In further exploration as anode materials for Lithium-ion batteries,the obtained carbon microspheres exhibit good cyclability and rate performance with a reversible capacity of 444 m Ah g^(-1)at 50 m A g^(-1).This work provides theoretical fundamentals for the controllable thermal transformation of biomass towards wide applications.展开更多
A novel modified poly(dl-lactic acid) (PDLLA) was obtained by covalently grafting of maleic anhydride onto the backbone of PDLLA, attempting to improve PDLLA’s hydrophilicity and cell affinity and to provide reactive...A novel modified poly(dl-lactic acid) (PDLLA) was obtained by covalently grafting of maleic anhydride onto the backbone of PDLLA, attempting to improve PDLLA’s hydrophilicity and cell affinity and to provide reactive groups for further chemical modification. FTIR, 13C NMR and DSC were used to characterize the maleic anhydride-modified PDLLA.展开更多
Poly(propylene carbonate phthalate)(PPC-P)is a chemically modified poly(propylene carbonate)(PPC)biodegradable thermoplastic by introducing phthalic anhydride(PA)as the third monomer into the copolymerization of propy...Poly(propylene carbonate phthalate)(PPC-P)is a chemically modified poly(propylene carbonate)(PPC)biodegradable thermoplastic by introducing phthalic anhydride(PA)as the third monomer into the copolymerization of propylene oxide(PO)and CO_(2).To enhance the thermal and mechanical properties of PPC-P,a branching agent pyromellitic anhydride(PMDA)was introduced into the terpolymerization of PO,PA and CO_(2).The resulting copolymers with branched structure,named branched PPC-P,can be obtained using metal-free Lewis pair consisting of triethyl borane(TEB)and bis(triphenylphosphine)iminium chloride(PPNCl)as catalyst.The products obtained were analyzed by NMR spectroscopy and their thermal,mechanical properties and melt processability were evaluated by DSC,TGA,tensile test and melt flow index(MFI)measurement.The obtained branched PPC-P has a high molecular weight up to 156.0 kg·mol^(-1).It shows an increased glass transition temperature(Tg)higher than 50℃and an enhanced tensile strength as high as 38.9 MPa.Noteworthily,the MFI value decreases obviously,indicative of an improved melt strength arising from the branched structure and high molecular weight.What is more,the branched PPC-P exhibits reasonable biodegradability,which demonstrates the great potential as a new green thermoplastic for the family of biodegradable plastics.展开更多
Mesoporous poly(styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis was achieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydrid...Mesoporous poly(styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis was achieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydride copolymer in the presence of 3-aminopropyl triethoxysilane (APTES) as a coupling agent and citric acid as a nonsurfactant template or pore-forming agent, followed by ethanol extraction. Characterization results from nitrogen sorption isotherms and powder X-ray diffraction indicate that polymer-modified mesoporous materials with large specific surface areas (e.g. 900 m(2)/g) and pore volumes (e.g. 0.6 cm(3)/g) could be prepared. As the citric acid concentration is increased, the specific surface areas, pore volumes and pore diameters of the hybrid materials increase.展开更多
Solid-liquid equilibria (SLE) of three binary systems and seventernary systems containing maleic an- hydride (MA) are measured byvisual method. The experimental data are compared with the calculatedones with modified ...Solid-liquid equilibria (SLE) of three binary systems and seventernary systems containing maleic an- hydride (MA) are measured byvisual method. The experimental data are compared with the calculatedones with modified universal quasichemical functional group activitycoefficient (UNIFAC) method in which the interaction parametersbetween groups come from two sources, dortmund data bank (DDB), ifthere's any, and correlations based on our former presentedexperimental SLE data of twenty binary systems.展开更多
Natural rubber grafted maleic anhydride （NR-g-MAH） was synthesized by mixing maleic anhydride （MAH） and natural rubber （NR） in solid state in a torque rheometer using dicurnyl peroxide （DCP） as initiator. Then...Natural rubber grafted maleic anhydride （NR-g-MAH） was synthesized by mixing maleic anhydride （MAH） and natural rubber （NR） in solid state in a torque rheometer using dicurnyl peroxide （DCP） as initiator. Then the self-prepared NR-g-MAH was used as a compatibilizer in the natural rubber/short nylon fiber composites. Both the fimctionalization of NR with MAH and the reaction between the modified rubber and the nylon fiber were confirmed by Fourier transform infrared spectroscopy （FTIR）. Composites with different nylon short fiber loadings （0, 5, 10, 15 and 20 phr） were compounded on a two-roll mill, and the effects of the NR-g-MAH on the tensile and thermal properties, fiber-rubber interaction, as well as the morphology of the natural rubber/short nylon fiber composites were investigated. At equal fiber loading, the NR-g-MAH compatibilized NR/short nylon fiber composites showed improved tensile properties, especially the tensile modulus at 100% strain which was about 1.5 times that of the corresponding un-compatibilized ones. The equilibrium swelling tests proved that the incorporation of NR-g-MAH increased the interaction between the nylon fibers and the NR matrix. The crosslink density measured with NMR techniques showed that the NR-g-MAH compatiblized composites had lower total crosslink density. The glass transition temperatures of the compatibilized composites were about 1 K higher than that of the corresponding un-compabilized ones. Morphology analysis of the NR/short nylon fiber composites confirmed NR-g-MAH improved interfacial bonding between the NR matrix and the nylon fibers. All these results signified that the NR-g-MAH could act as a good compatilizer of NR/short nylon fiber composites and had a potential for wide use considering its easy to be prepared and compounded with the composites.展开更多
Tetrahydrofuran ring can be opened with acyl chlorides or anhydrides catalyzed by gallium triiodides to afford iodo esters under mild conditions in good yields.
Ring opening copolymerization of succinic anhydride (SA) with ethylene oxide (EO)was successfully carried out by using a series of aluminum-based catalyst in 1,4-dioxane at62±2℃. The results showed that in-situ ...Ring opening copolymerization of succinic anhydride (SA) with ethylene oxide (EO)was successfully carried out by using a series of aluminum-based catalyst in 1,4-dioxane at62±2℃. The results showed that in-situ AlR_3-H_2O (R=ethyl, iso-butyl) catalysts gavehigher molecular weight (M_w～10~4), while Al(OR)_3 catalysts gave the higher alternatingcopolymer structure with slightly lower molecular weight. The in-situ AlR_3-H_2O systemshave been evaluated in more detail for the reaction which showed the optimum H_2O/Almolar ratio to be 0.5. The copolymers with different composition (F_(SA)/F_(EO)= 36/64to 45/55 mol/mol) were synthesized by using different monomer feed ratio. The melt-ing point (T_m), glass transition temperature (T_g) and enthalpy of fusion (ΔH_f) of thesecopolymers are depended on the copolymer composition and in the range of 87～102℃,-12～-18℃, and 37～66J/g, respectively. The second heating scan of DSC also in-dicated that the higher alternating copolymer was more easily recrystallized. The onsetdecomposition temperature was more than 300℃ under nitrogen and influenced by thecopolymer composition.展开更多
Au/FeOx-TiO2,prepared by deposition-precipitation method,is an efficient and stable catalyst for the liquid phase selective hydrogenation of phthalic anhydride to phthalide under mild reaction conditions.
The synthesis of block copolymers of poly(tetrahydrofuran)-b-poly(α-amino acid)(PTHF-b-PAA)is challenging since it is difficult to combine the two blocks produced via different/conflicting ring-opening polymerization...The synthesis of block copolymers of poly(tetrahydrofuran)-b-poly(α-amino acid)(PTHF-b-PAA)is challenging since it is difficult to combine the two blocks produced via different/conflicting ring-opening polymerization(ROP)mechanisms.In this contribution,the cationic ROP of THF is catalyzed by rare-earth triflate[RE(OTf)3]and terminated by 2-(t-butyloxycarbonyl-amino)ethanol(BAE).After the deprotection of t-butyloxycarbonyl(Boc)group,the chain end of PTHF is quantitatively changed to amino group which thereafter initiates the nucleophilic ROP ofα-amino acid N-thiocarboxyanhydrides(NTAs).Both polymerizations are well controlled,generating PTHF and PAA segments with designable molecular weights(MWs).PTHF-b-polylysine(PTHF-b-PLys)and PTHF-b-polysarcosine(PTHF-b-PSar)are obtained with MWs between 8.6 and 28.7 kg/mol.The above amphiphilic diblock copolymers form micelles in water.PTHF40-b-PSar32 acts as a surfactant to stabilize oil-in-water emulsions.Both segments of PTHF-b-PAA are biocompatible and promising in the biomedical application.展开更多
A novel poly (amide-imide) was prepared from a novel monomer: 5,6-diphenyl-chloroformyl-3,4-benzenedicarboxylic anhydride and bis (4-aminophenyl) ether. The polymer was characterized by FTIR. (HNMR)-H-1. DSC and TGA.
Pd catalysts suffered from poor selectivity and stability for liquid-phase hydrogenation of maleic anhydride（MA） to gamma-butyrolactone（GBL）.Thus,Pd/C catalysts modified with different Sn loadings were synthesized...Pd catalysts suffered from poor selectivity and stability for liquid-phase hydrogenation of maleic anhydride（MA） to gamma-butyrolactone（GBL）.Thus,Pd/C catalysts modified with different Sn loadings were synthesized,and characterized by XRD,XPS,TEM and elemental mapping.The types of alloy phase and the amounts of the surface Pd-SnOx sites altered along with Sn/Pd mass ratios from 0-1.0synthesized in the process of preparation.The maximum reaction rate was 0.57 mol-GBL/（mol-Pd min）and selectivity was 95.94%when the Sn/Pd mass ratio was 0.6.It might be attributed to the formation of Pd2Sn alloy and less amounts of Pd-SnOx sites.展开更多
基金supports for this work are the Inner Mongolia Major Science and Technology Project(No.2020ZD0024)Natural Science Foundation of Inner Mongolia(No.2024LHMS05046)+5 种基金Local Science and Technology Development Project of the Central Government(Nos.2021ZY0006 and 2022ZY0011)2023 Inner Mongolia Autonomous Region Doctoral Research Innovation Project(No.B20231023Z)Inner Mongolia Autonomous Region key Research and Technological Achievements Transformation Plan Project(No.2023YFHH0063)Autonomous Region higher education Carbon peak carbon neutral research project(No.STZX202206)Basic Scientific Research Expenses Program of Universities directly under Inner Mongolia Autonomous Region(No.JY20220043)Graphite and Graphene New Materials Discipline Team of Inner Mongolia University of Technology(No.PY202066).
文摘Paraphenylenediamine(PPDA)-grafted maleic anhydride(MAH)-modified graphene oxide(PGO)was synthesized through a dual modification process.Initially,MAH was employed to modify graphene oxide(GO)to enhance its reactive sites.Subsequently,PPDA was utilized for further modification of MAH-modified GO(MGO).Through a comprehensive analysis,the successful grafting of MAH and PPDA onto GO was confirmed.It was concurrently established that the optimal ratio of PPDA to MGO is 1:1.This approach yielded PGO characterized by outstanding dispersibility and barrier properties in epoxy resin(EP)coaings for Q235 steel.The corrosion resistance of EP coatings containing varying amounts of PGO was assessed using electrochemical workstation and salt spray testing.After immersing in a 3.5 wt.%NaCl solution for 300 h,the composite coating containing 0.1 wt.%PGO exhibited superior performance in terms of low-frequency impedance modulus,measuring at 1.1×10^(8)Ωcm^(2).The lowest corrosion current density was 2.32×10^(–10)A cm^(−2),and the self-corrosion voltage was−0.301 V.Additionally,polarization testing indicated that this coating also displayed the lowest corrosion rate,specifically 1.383×10^(–7)mm/a.
基金financially supported by the National Key R&D Program of China(No.2021YFA1501700)the Science and Technology Development Plan of Jilin Province(Nos.20230101042JC and 20210201059GX)+1 种基金the National Natural Science Foundation of China,Basic Science Center Program(No.51988102)the National Natural Science Foundation of China(Nos.52203017 and 52073272)。
文摘Chemical modification of polymers represents a pivotal method for achieving functionalized polymer materials.However,due to the lack of post-functional handle,the chemical modification of polyester materials remains a significant challenge.Ring-opening copolymerization of cyclic anhydride and epoxides is a powerful approach to synthesize polyesters.In this work,we for the first time demonstrate the functionalizability of polyesters synthesized with brominated anhydride monomers.The post-functionalization is amenable to a wide variety of reactive groups and reactions with high yields.With multiple well-established functionalization pathways of brominated polyester materials and optimized the conditions for the modification reactions,a series of functionalized polyester materials can be obtained with high yields,providing new insights for the research about functionalization of polymers.
基金supported by National Key R&D Program of China(2019YFA0110600)National Natural Science Foundation of China(82370929,81970916)+2 种基金Sichuan Science and Technology Program(2022NSFSC0002)Sichuan Province Youth Science and Technology Innovation Team(2022JDTD0021)Research and Develop Program,West China Hospital of Stomatology Sichuan University(RD03202302)。
文摘Bacterial resistance and excessive inflammation are common issues that hinder wound healing.Antimicrobial peptides(AMPs)offer a promising and versatile antibacterial option compared to traditional antibiotics,with additional anti-inflammatory properties.However,the applications of AMPs are limited by their antimicrobial effects and stability against bacterial degradation.TFNAs are regarded as a promising drug delivery platform that could enhance the antibacterial properties and stability of nanodrugs.Therefore,in this study,a composite hydrogel(HAMA/t-GL13K)was prepared via the photocross-linking method,in which tFNAs carry GL13K.The hydrogel was injectable,biocompatible,and could be instantly photocured.It exhibited broad-spectrum antibacterial and anti-inflammatory properties by inhibiting the expression of inflammatory factors and scavenging ROS.Thereby,the hydrogel inhibited bacterial infection,shortened the wound healing time of skin defects in infected skin full-thickness defect wound models and reduced scarring.The constructed HAMA/tFNA-AMPs hydrogels exhibit the potential for clinical use in treating microbial infections and promoting wound healing.
基金supported by the National Natural Science Foundation of China(21173050,21371035)SINOPEC(X514005)~~
文摘Ni/Al2O3 catalysts were derived from spinel NiAl2O4 with different Ni content ((2.5, 5 and 7.5) wt%). The catalysts were obtained by H-2 reduction and were investigated for the low-temperature hydrogenation of maleic anhydride (MA) to produce succinic anhydride (SA). The characterization results showed that Ni-0 active sites were mainly derived during the H2 reduction from spinel NiAl2O4 Among the catalysts studied, employing the optimum preparation and reaction conditions with Ni(5%)/Al2O3 yielded the highest catalytic performance. A near-100% conversion of MA and similar to 90% selectivity to SA were achieved at 120 degrees C and 0.5 MPa of H-2 with a weighted hourly space velocity (MA) of 2 h(-1). (C) 2017, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
基金supported by the National Natural Science Foundation of China (Nos. 21173050 and 21371035)China Petrochemical Corporation (No. X514005)
文摘The pseudo-boehmite derived alumina supported metal（Cu,Co and Ni） catalysts prepared by the impregnation method were investigated in hydrogenation of maleic anhydride（MA） to succinic anhydride（SA） and γ-butyrolactone.The catalysts were characterized by ICP-AES,N2 adsorptiondesorption,XRD,H2-TPR,CO-TPD,dissociative N2O adsorption and TEM and the results showed that the alumina possessed mesoporous feature and the metal species were well dispersed on the support.Compared to Cu/Al2O3 and Co/Al2O3,Ni/Al2O3 exhibited higher catalytic activity in the MA hydrogenation with 92%selectivity to SA and nearly 100%conversion of MA at 140 °C under 0.5 MPa of H2 with a weighted hourly space velocity of 2 h 1（MA）.The stability of Ni/Al2O3 catalyst was also investigated.
文摘In this work, the hydrogenation of maleic anhydride to succinic anhydride in the presence of 5 m%Ni/clay catalysts was investigated. These catalysts were characterized by X-ray diffraction （XRD）, H2 temperature programmed reduction （TPR） and thermogravimetric analysis （TGA） techniques. The XRD and TPR studies showed that Ni was present as Ni2＋ on the support, which indicated that there were no elemental nickel （Ni^0） and Ni203 species in the unreduced samples. Increasing of calcination temperature to 650 ℃ leads to destruction of the support structure observed in TGA, while the catalyst sample calcined at 550 ℃ exhibits better performances than other samples. The ideal conversion of maleic anhydride （97.14%） and selectivity of succinic anhydride （99.55%） were realized at a reaction temperature of 180 ℃ and a weight hourly space velocity of 4 h^-1 under a reaction pressure of 1 MPa.
基金The authors are grateful for the financial supports of the Project of Research and Development Fund of Nanchong City(19YFZJ0107,18YFZJ0041)the Meritocracy Research Funds of China West Normal University(17YC041)the Undergraduate Training Program for Innovation of China West Normal University.(cxcy2020186).
文摘The colloidal carbon microspheres(CMS)were prepared by the hydrothermal method.The nickel catalysts supported on carbon microspheres(Ni/CMS)were further prepared and were characterized by the Fourier transform infrared spectroscopy(FTIR),the X-ray diffraction(XRD),the scanning electron microscopy(SEM),the transmission electron microscopy(TEM),and the N_(2)adsorption technique.The selective hydrogenation of maleic anhydride(MA)to succinic anhydride(SA)over the Ni/CMS catalysts was investigated.The results indicated that the Ni/CMS catalyst,which was prepared with glucose as carbon source and calcined at 500℃,exhibited the best performance.The hydrogen pressure,reaction temperature,and reaction time could significantly affect the conversion of maleic anhydride during the hydrogenation reaction.A 98.4%conversion of MA and an 100%selectivity to SA were achieved over the Ni/CMS catalyst in acetic anhydride solvent under mild conditions covering a temperature of 90℃,a H2 pressure of 1.0 MPa,and a reaction time of 3 h.
基金supported by the National Natural Science Foundation of China(Nos.21772022,and 22171124)Minjiang University(No.MJY21041)Fuzhou University.
文摘Fluoroalkyl-containing organic compounds have exhibited wide applications in the field of pharmaceuticals,agrochemicals and materials science due to their outstanding properties such as biological activity,metabolic stability,lipophilicity,excellent chemical and thermal stability.Therefore,various synthetic strategies have been developed for the construction of fluoroalkyl-containing compounds,using highly active fluorinating reagents and fluorinated building blocks.Recently,the use of easily available and inexpensive trifluoroacetic anhydride(TFAA)and its anhydride analogues has attracted great attention to access numerous fluoroalkyl-containing compounds through cyclization and coupling reactions.In this review,we summarized the recent advances in the synthesis of fluoroalkylated compounds using fluoroalkyl anhydrides as reagents.This review aims to provide a reference for researchers on how to develop new synthetic straregies of fluorine-containing organic compounds and achieve kilograms or even tons preparation of fluorine-containing organic compounds using fluoroalkyl anhydrides.
基金supported by the National Science Foundation for Excellent Young Scholars of China(21922815)the Key Research and Development(R&D)Projects of Shanxi Province(201903D121180)the National Key Research and Development(R&D)Program of China。
文摘Starch,as a typical polysaccharide with natural spherical morphology,is not only a preferred precursor for preparing carbon materials but also a model polymer for investigating thermochemical evolution mechanisms.However,starch usually suffers from severe foaming and low carbon yield during direct pyrolysis.Herein,we report a simple and eco-friendly dry strategy,by maleic anhydride initiating the esterification of starch,to design carbon microspheres against the starch foaming.Moreover,the infuence of ester grafting on the pyrolytic behavior of starch is also focused.The formation of ester groups in precursor guarantees the structural stability of starch-based intermediate because it can promote the accumulation of unsaturated species and accelerate the water elimination during pyrolysis.Meanwhile,the esterification and dehydration reactions greatly deplete the primary hydroxyl groups in the starch molecules and thus the rapid levoglucosan release is inhibited,which well keeps the spherical morphology of starch and ensures the high carbon yield.In further exploration as anode materials for Lithium-ion batteries,the obtained carbon microspheres exhibit good cyclability and rate performance with a reversible capacity of 444 m Ah g^(-1)at 50 m A g^(-1).This work provides theoretical fundamentals for the controllable thermal transformation of biomass towards wide applications.
文摘A novel modified poly(dl-lactic acid) (PDLLA) was obtained by covalently grafting of maleic anhydride onto the backbone of PDLLA, attempting to improve PDLLA’s hydrophilicity and cell affinity and to provide reactive groups for further chemical modification. FTIR, 13C NMR and DSC were used to characterize the maleic anhydride-modified PDLLA.
基金financially supported by the National Natural Science Foundation of China(No.51673131)the Fundamental Research Funds for the Central Universities(No.171gjc37)。
文摘Poly(propylene carbonate phthalate)(PPC-P)is a chemically modified poly(propylene carbonate)(PPC)biodegradable thermoplastic by introducing phthalic anhydride(PA)as the third monomer into the copolymerization of propylene oxide(PO)and CO_(2).To enhance the thermal and mechanical properties of PPC-P,a branching agent pyromellitic anhydride(PMDA)was introduced into the terpolymerization of PO,PA and CO_(2).The resulting copolymers with branched structure,named branched PPC-P,can be obtained using metal-free Lewis pair consisting of triethyl borane(TEB)and bis(triphenylphosphine)iminium chloride(PPNCl)as catalyst.The products obtained were analyzed by NMR spectroscopy and their thermal,mechanical properties and melt processability were evaluated by DSC,TGA,tensile test and melt flow index(MFI)measurement.The obtained branched PPC-P has a high molecular weight up to 156.0 kg·mol^(-1).It shows an increased glass transition temperature(Tg)higher than 50℃and an enhanced tensile strength as high as 38.9 MPa.Noteworthily,the MFI value decreases obviously,indicative of an improved melt strength arising from the branched structure and high molecular weight.What is more,the branched PPC-P exhibits reasonable biodegradability,which demonstrates the great potential as a new green thermoplastic for the family of biodegradable plastics.
基金Project supported by the National Natural Science Foundation of China (No. 29874002) and the Outstanding Young Scientist Award from National Natural Science Foundation of China (No. 29825504)
文摘Mesoporous poly(styrene-co-maleic anhydride)/silica hybrid materials have been prepared. The synthesis was achieved by the HCl-catalyzed sol-gel reactions of tetraethyl orthosilicate (TEOS) and styrene-maleic anhydride copolymer in the presence of 3-aminopropyl triethoxysilane (APTES) as a coupling agent and citric acid as a nonsurfactant template or pore-forming agent, followed by ethanol extraction. Characterization results from nitrogen sorption isotherms and powder X-ray diffraction indicate that polymer-modified mesoporous materials with large specific surface areas (e.g. 900 m(2)/g) and pore volumes (e.g. 0.6 cm(3)/g) could be prepared. As the citric acid concentration is increased, the specific surface areas, pore volumes and pore diameters of the hybrid materials increase.
文摘Solid-liquid equilibria (SLE) of three binary systems and seventernary systems containing maleic an- hydride (MA) are measured byvisual method. The experimental data are compared with the calculatedones with modified universal quasichemical functional group activitycoefficient (UNIFAC) method in which the interaction parametersbetween groups come from two sources, dortmund data bank (DDB), ifthere's any, and correlations based on our former presentedexperimental SLE data of twenty binary systems.
基金financially supported by the Joint Funds of the National Natural Science Foundation of China and Guangdong Province(No.U1134005)
文摘Natural rubber grafted maleic anhydride （NR-g-MAH） was synthesized by mixing maleic anhydride （MAH） and natural rubber （NR） in solid state in a torque rheometer using dicurnyl peroxide （DCP） as initiator. Then the self-prepared NR-g-MAH was used as a compatibilizer in the natural rubber/short nylon fiber composites. Both the fimctionalization of NR with MAH and the reaction between the modified rubber and the nylon fiber were confirmed by Fourier transform infrared spectroscopy （FTIR）. Composites with different nylon short fiber loadings （0, 5, 10, 15 and 20 phr） were compounded on a two-roll mill, and the effects of the NR-g-MAH on the tensile and thermal properties, fiber-rubber interaction, as well as the morphology of the natural rubber/short nylon fiber composites were investigated. At equal fiber loading, the NR-g-MAH compatibilized NR/short nylon fiber composites showed improved tensile properties, especially the tensile modulus at 100% strain which was about 1.5 times that of the corresponding un-compatibilized ones. The equilibrium swelling tests proved that the incorporation of NR-g-MAH increased the interaction between the nylon fibers and the NR matrix. The crosslink density measured with NMR techniques showed that the NR-g-MAH compatiblized composites had lower total crosslink density. The glass transition temperatures of the compatibilized composites were about 1 K higher than that of the corresponding un-compabilized ones. Morphology analysis of the NR/short nylon fiber composites confirmed NR-g-MAH improved interfacial bonding between the NR matrix and the nylon fibers. All these results signified that the NR-g-MAH could act as a good compatilizer of NR/short nylon fiber composites and had a potential for wide use considering its easy to be prepared and compounded with the composites.
基金the National Natural Science Foundation of China !298720I0the NSF of she-hang Provincethe Laboratory of Organometallic Ch
文摘Tetrahydrofuran ring can be opened with acyl chlorides or anhydrides catalyzed by gallium triiodides to afford iodo esters under mild conditions in good yields.
文摘Ring opening copolymerization of succinic anhydride (SA) with ethylene oxide (EO)was successfully carried out by using a series of aluminum-based catalyst in 1,4-dioxane at62±2℃. The results showed that in-situ AlR_3-H_2O (R=ethyl, iso-butyl) catalysts gavehigher molecular weight (M_w～10~4), while Al(OR)_3 catalysts gave the higher alternatingcopolymer structure with slightly lower molecular weight. The in-situ AlR_3-H_2O systemshave been evaluated in more detail for the reaction which showed the optimum H_2O/Almolar ratio to be 0.5. The copolymers with different composition (F_(SA)/F_(EO)= 36/64to 45/55 mol/mol) were synthesized by using different monomer feed ratio. The melt-ing point (T_m), glass transition temperature (T_g) and enthalpy of fusion (ΔH_f) of thesecopolymers are depended on the copolymer composition and in the range of 87～102℃,-12～-18℃, and 37～66J/g, respectively. The second heating scan of DSC also in-dicated that the higher alternating copolymer was more easily recrystallized. The onsetdecomposition temperature was more than 300℃ under nitrogen and influenced by thecopolymer composition.
基金support provided by Zhejiang Provincial Natural Science Foundation of China(No.Y405108)the Department of Education of Zhejiang Province of China(No.20051409)
文摘Au/FeOx-TiO2,prepared by deposition-precipitation method,is an efficient and stable catalyst for the liquid phase selective hydrogenation of phthalic anhydride to phthalide under mild reaction conditions.
基金Joint Foundation of Shaanxi Province Natural Science Basic Research Program and Shaanxi Coal Chemical Group Co.,Ltd.(No.2019JLM-46)the National Natural Science Foundation of China(No.21674091).
文摘The synthesis of block copolymers of poly(tetrahydrofuran)-b-poly(α-amino acid)(PTHF-b-PAA)is challenging since it is difficult to combine the two blocks produced via different/conflicting ring-opening polymerization(ROP)mechanisms.In this contribution,the cationic ROP of THF is catalyzed by rare-earth triflate[RE(OTf)3]and terminated by 2-(t-butyloxycarbonyl-amino)ethanol(BAE).After the deprotection of t-butyloxycarbonyl(Boc)group,the chain end of PTHF is quantitatively changed to amino group which thereafter initiates the nucleophilic ROP ofα-amino acid N-thiocarboxyanhydrides(NTAs).Both polymerizations are well controlled,generating PTHF and PAA segments with designable molecular weights(MWs).PTHF-b-polylysine(PTHF-b-PLys)and PTHF-b-polysarcosine(PTHF-b-PSar)are obtained with MWs between 8.6 and 28.7 kg/mol.The above amphiphilic diblock copolymers form micelles in water.PTHF40-b-PSar32 acts as a surfactant to stabilize oil-in-water emulsions.Both segments of PTHF-b-PAA are biocompatible and promising in the biomedical application.
文摘A novel poly (amide-imide) was prepared from a novel monomer: 5,6-diphenyl-chloroformyl-3,4-benzenedicarboxylic anhydride and bis (4-aminophenyl) ether. The polymer was characterized by FTIR. (HNMR)-H-1. DSC and TGA.
基金supported by the National Natural Science Foundation,China(Nos.21506138,21606199,21575097 and21375092)the Natural Science Foundation of Zhejiang Province,China(No.LQ15B060001)the China Postdoctoral Science Foundation(No.2016M592015)
文摘Pd catalysts suffered from poor selectivity and stability for liquid-phase hydrogenation of maleic anhydride（MA） to gamma-butyrolactone（GBL）.Thus,Pd/C catalysts modified with different Sn loadings were synthesized,and characterized by XRD,XPS,TEM and elemental mapping.The types of alloy phase and the amounts of the surface Pd-SnOx sites altered along with Sn/Pd mass ratios from 0-1.0synthesized in the process of preparation.The maximum reaction rate was 0.57 mol-GBL/（mol-Pd min）and selectivity was 95.94%when the Sn/Pd mass ratio was 0.6.It might be attributed to the formation of Pd2Sn alloy and less amounts of Pd-SnOx sites.
