Zinc phenylphosphonate （PPZn）, a benign and biocompatible nucleating agent, was prepared and incorporated into the biodegradable poly（ethylene adipate） （PEA） to investigate its effect on the crystallization beha...Zinc phenylphosphonate （PPZn）, a benign and biocompatible nucleating agent, was prepared and incorporated into the biodegradable poly（ethylene adipate） （PEA） to investigate its effect on the crystallization behavior, crystallization kinetics and spherulite morphology of PEA. Upon addition of PPZn, the crystallization temperature and crystallinity of PEA in the non-isothermal crystallization process increased significantly. Analysis of crystallization kinetics by Avrami equation suggests that the crystallization time shortened greatly and crystallization rate increased markedly after addition of PPZn. In the presence of PPZn, the spherulite size decreased and spherulite density increased significantly. It suggests that PPZn is an efficient nucleating agent for the crystallization of PEA. The accelerated crystallization in the presence of PPZn is mainly attributed to the epitaxial nucleation of PEA crystals on the surface of PPZn crystals, that is, a perfect lattice matching between PEA crystal and PPZn crystal occurs.展开更多
The effects of crystallization temperature and blend ratio on the polymorphic crystal structures of poly（butylene adipate） （PBA） in poly（butylene succinate） （PBS）/poly（butylene adipate） （PBS/PBA） blends we...The effects of crystallization temperature and blend ratio on the polymorphic crystal structures of poly（butylene adipate） （PBA） in poly（butylene succinate） （PBS）/poly（butylene adipate） （PBS/PBA） blends were studied by means of differential scanning calorimetry （DSC）, wide-angle X-ray diffraction （XRD） and atomic force microscopy （AFM）. It was revealed that the polymorphism of PBA can be regulated by the blend ratio even in a non-isothermal crystallization process. The results demonstrate that high temperature favors fiat-on α crystals, while low temperature contributes to edge-on β crystals. It was also found that the effect of blend ratio on the crystallization mechanism of PBA is well coincident with that of the crystallization temperature. The increment of PBS content in the PBS/PBA blend gives rise to more β-form crystals of PBA. For those PBS/PBA blends with low PBA content, the interlamellar phase segregation of PBA makes its molecular chains so difficult to diffuse from one isolated microdomain to another that high crystallization temperature and sufficiently long crystallization time will be required if the PBA α-type crystals are targeted.展开更多
The crystallization behavior of poly（ethylene adipate） （PEA） on highly oriented high-density polyethylene （PE） substrate both from solution and isotropic melt was studied by means of optical microscopy, differen...The crystallization behavior of poly（ethylene adipate） （PEA） on highly oriented high-density polyethylene （PE） substrate both from solution and isotropic melt was studied by means of optical microscopy, differential scanning calorimetry, atomic force microscopy and electron diffraction. The results show that the PE influences the crystallization of PEA strongly, which results in an epitaxial growth of PEA with well ordered structure. At the boundary of the PE substrate, a transcrystalline PEA layer is observed. Fine structural observation illustrates that the PEA grows on the PE substrate in edge- on lamellae with fixed orientation. Electron diffraction demonstrates that the epitaxial organization of PEA on PE occurs with both polymer chains parallel, which leads to the （00l） PEA diffractions inclined ±23.5° to the chain direction of PE crystals. Combining the real space morphological observation and electron diffraction results, it is concluded that the epitaxial PEA edge-on lamellae are folded in the {00l} lattice planes.展开更多
The miscibility, isothermal crystallization kinetics and morphology of the poly（vinylidene fluoride）（PVDF）/poly（ethylene adipate）（PEA） blends have been studied by differential scanning calorimetry（DSC）, opti...The miscibility, isothermal crystallization kinetics and morphology of the poly（vinylidene fluoride）（PVDF）/poly（ethylene adipate）（PEA） blends have been studied by differential scanning calorimetry（DSC）, optical microscopy（OM） and scanning electron microscopy（SEM）. A depression of the equilibrium melting point of PVDF was observed. From the melting point data of PVDF, a negative but quite small value of the interaction parameter ？PVDF-PEA is derived using the Flory-Huggins equation, implying that PVDF shows miscibility with PEA to some extent. Nonisothermal and isothermal crystallization kinetics suggest that the crystallization rate of PVDF decreases with increasing the amount of PEA, and a contrary trend was found when PEA crystallizes with the increase of the amount of PVDF. It was further disclosed that the blend ratio and crystallization temperature affect the texture of PVDF spherulites greatly, which determines the subsequent crystallization of PEA. At high temperatures, e.g. 150 ℃, the band spacing of PVDF spherulites increases with the addition of PEA content and the spherulitic structure becomes more open. In this case, spherulitic crystallization of PEA is not observed for all blend compositions. At low temperatures, e.g. 130 ℃, for the PEA-rich blends, the interpenetrated structures are eventually formed by the penetration of the spherulites of PEA growing within the pre-existing PVDF spherulites.展开更多
Oriented and non-oriented Teflon films, which were found to have the same crystalline structure, but different surface morphologies, were used to sandwich poly（butylene adipate） （PBA） films during isothermal cryst...Oriented and non-oriented Teflon films, which were found to have the same crystalline structure, but different surface morphologies, were used to sandwich poly（butylene adipate） （PBA） films during isothermal crystallization. It was found that both the Teflon surface structure and the PBA polymorphic structure are the determining factors to induce epitaxial crystallization. The oriented Teflon film was able to induce epitaxial crystallization of PBA α crystal, while the non-oriented Teflon did not induce any epitaxial crystallization of PBA. Epitaxial crystallization did not occurred for PBA β crystals between neither the oriented nor the non-oriented Teflon films. The enzymatic degradation rate of PBA films was not determined by the epitaxial crystallization, in fact it was still dependent on the polymorphic crystal structure of PBA. The morphological changes of PBA films after enzymatic degradation confirmed again that the epitaxial crystallization only occurred for the PBA film with α crystal structure which was produced by being sandwiched between oriented Teflon films, and it happened only on the surface of PBA films.展开更多
The effects of PEA on the ）γ-phase PVDF crystal structure and the crystallization of PEA within the pre-existing γ-phase PVDF spherulites have been investigated by optical microscopy （OM）, infrared spectroscopy ...The effects of PEA on the ）γ-phase PVDF crystal structure and the crystallization of PEA within the pre-existing γ-phase PVDF spherulites have been investigated by optical microscopy （OM）, infrared spectroscopy （IR） and scanning electron microscopy （SEM）. The results demonstrate that the γ-phase PVDF spherulites consist of the lamellae exhibiting a highly curved scroll-like morphology and develop preferentially in PEA-rich blend. With increasing PEA concentration, the scroll diameter increases and the scrolls are better separated from each other. PEA crystallizes first in the interspherulitic region and transcrystalline layer develops. Subsequently, the transcrystalline layer of PEA continues to grow within theγ-phase PVDF spherulites, e.g., in the region between the scrolls, until impinging on other PEA transcrystalline layers or spherulites. The crystallization kinetics results indicate that the growth rate of PEA crystals in the intraspherulitic region of γ-phase PVDF shows a positive correlation with content of PEA, but a negative one with the crystallization temperature of γ-phase PVDF.展开更多
Poly(glycolic acid)(PGA)is derived from glycolide obtained by fermenting pineapples or sugarcane,which has excellent gas barrier properties and a small carbon footprint.PGA is a potential substitute for the current al...Poly(glycolic acid)(PGA)is derived from glycolide obtained by fermenting pineapples or sugarcane,which has excellent gas barrier properties and a small carbon footprint.PGA is a potential substitute for the current aluminum-plastic composite films used in high barrier packaging applications.However,its poor ductility and narrow processing window limit its application in food packaging.Herein,poly(butylene succinate-co-butylene adipate)(PBSA)was used to fabricate PGA/PBSA blend films through an in situ fibrillation technique and blown film extrusion.Under the elongational flow field used during the extrusion process,a unique hierarchical structure based on the PBSA nanofibrils and interfacially oriented PGA crystals was obtained.This structure enhances the strength,ductility and gas barrier properties of the PGA/PBSA blend film.In addition,an epoxy chain extender(ADR4468)was used as a compatibilizer to further enhance the interfacial adhesion between PGA and PBSA.70PGA/0.7ADR exhibited a very low oxygen permeability(2.34×10^(-4)Barrer)with significantly high elongating at break(604.4%),tensile strength(47.4 MPa),and transparency,which were superior to those of petroleum-based polymers.Thus,the 70PGA/0.7ADR blown films could satisfy the requirements for most instant foods such as coffee,peanuts,and fresh meat.展开更多
In the present study,thermal behavior and crystal transition of pure poly(butylene adipate)(PBA)upon heating process were investigated by FTIR spectroscopy.To gain further insight into the thermal behavior alteration ...In the present study,thermal behavior and crystal transition of pure poly(butylene adipate)(PBA)upon heating process were investigated by FTIR spectroscopy.To gain further insight into the thermal behavior alteration and the phase transition of PBA,we performed two-dimensional(2D)correlation analysis.We found thatβ-form PBA crystal undergoes not only the melting process but also crystal transition upon the heating process.展开更多
We successfully use a co-precipitation method to prepare inclusion complex between poly（butylene adipate） （PBA） chains （vip component） and urea molecules （host component）. The PBA/urea inclusion complex is c...We successfully use a co-precipitation method to prepare inclusion complex between poly（butylene adipate） （PBA） chains （vip component） and urea molecules （host component）. The PBA/urea inclusion complex is confirmed to adopt a hexagonal crystal modification with lattice parameters ofa = 8.14 A and c = 10.92 A, and the interaction between PBA chains and urea is van der Waals force. The singly isolated PBA chains are suggested to take some gauche conformation, which is different from the all-trans conformation in r-form PBA. Furthermore, we employ the isolated PBA chains which are uniformly pre-established in a specific conformation in urea channels to regulate the crystal form of PBA for the first time. After removing the host urea molecules, the coalesced PBA chains are found to solely crystallize into a-form crystals at different coalescing temperatures. By comparing the FTIR spectra, it is found that PBA chains in inclusion complex plausibly contain some similar conformers as those in a-form crystal, which is suggested to be the intrinsic reason for the sole formation of a-form crystals. This research proves that inclusion complex can be used as a very effective method to regulate polymorphism of semi-crystalline polymers.展开更多
The ester base oil of dioctyl adipate (DOA) was oxidized in an oven at 200 degrees C for 30 h, and variations in the physicochemical and tribological properties were studied. To investigate the thermal-oxidation mecha...The ester base oil of dioctyl adipate (DOA) was oxidized in an oven at 200 degrees C for 30 h, and variations in the physicochemical and tribological properties were studied. To investigate the thermal-oxidation mechanism, the thermal-oxidation products were analyzed by gas chromatography-mass spectrometry (GC-MS), and the thermal-oxidation process was simulated using visual reactive force field molecular dynamics (ReaxFF MD). The results indicated that the total acid number (TAN) increased significantly because of the presence of 14% carboxylic acids and low molecular weight monoesters. The tribological properties were improved by the formation of the strongly polar carboxylic acids. Additionally, the increase in kinematic viscosity was limited due to the formation of high molecular weight polymerization products and low molecular weight degradation products. Thermal-oxidative degradation and polymerization mechanisms were proposed by combining ReaxFF MD simulations and GC-MS results.展开更多
A facile route for the synthesis of dimethyl adipate （DAP） from cyclopentanone and dimethyl carbonate （DMC） in the pres- ence of solid base catalysts has been developed. It was found that the intermediate carbomet...A facile route for the synthesis of dimethyl adipate （DAP） from cyclopentanone and dimethyl carbonate （DMC） in the pres- ence of solid base catalysts has been developed. It was found that the intermediate carbomethoxycyclopentanone （CMCP） was produced from cyclopentanone with DMC in the first step, and then CMCP was further converted to DAP by reacting with a methoxide group. The role of the basic catalysts can be mainly ascribed to the activation of cyclopentanone via the abstraction of a proton in the a-position by base sites, and solid bases with moderate strength, such as MgO, favor the formation of DAP.展开更多
In this manuscript,we conveniently prepared a series of polyester-polycarbonate copolymer(PPC-P)/polybutylene adipate terephthalate(PBAT)blends that exhibit both flame-retardant properties and toughness.Piperazine pyr...In this manuscript,we conveniently prepared a series of polyester-polycarbonate copolymer(PPC-P)/polybutylene adipate terephthalate(PBAT)blends that exhibit both flame-retardant properties and toughness.Piperazine pyrophosphate(PAPP),melamine phosphate(MPP)and ZnO were used as synergistic flame retardants for PPC-P/PBAT blends.The effects of synergistic flame retardants on thermal stability,combustion behavior and flame retardancy of PPC-P/PBAT blends were investigated.The results showed that when the ratio of PAPP/MPP/ZnO was 18.4:9.2:2.4,the LOI of PPC-P/PBAT composite was 42.8%,and UL-94 reached V-0 level.The results of cone calorimetry showed that the mass loss rate(MLR),the peak value of the biggest smoke production rate(pSPR)and total smoke production(TSP)of the material decreased,and a continuously expanded carbon layer with a compact structure was formed after combustion.The carbon layer formed after surface combustion protects the material from decomposition over a long temperature range.In terms of mechanical properties,compared with the composites with only PAPP and MPP,PAPP/MPP/ZnO composites can improve the mechanical properties.After adding 2.4 wt% ZnO,the tensile strength and impact strength of the polymer increased to 34.2 MPa and 28.5 kJ/m^(2),respectively.The results showed that the use of non-toxic,environmentally friendly,halogen-free flame retardants to enhance the flame retardant properties of biodegradable polymer composites is a promising direction in the future.展开更多
Nitrous oxide(N_(2)O),as an important gas affecting climate warming,is attracting attention from allwalks of life.This reviewaddresses N_(2)O emissions status in the adipic acid industry,a significant industrial green...Nitrous oxide(N_(2)O),as an important gas affecting climate warming,is attracting attention from allwalks of life.This reviewaddresses N_(2)O emissions status in the adipic acid industry,a significant industrial greenhouse gas source.It elucidates the N_(2)O emission mechanism and influencing factors in adipic acid production.It extensively evaluates N_(2)O emission accounting methods,including Intergovernmental Panel on Climate Change(IPCC)Guidelines,World Resources Institute(WRI)Protocol,and others.While the IPCC emission factor method offers simplicity and comparability,it may lack precision for facilities with advanced emission reduction measures.To address this,a combined modeling and monitoring approach is advocated.It scrutinizes modeling methods(statistical techniques,Greenhouse Gas and Air Pollution Interactions and Synergies,and Life-cycle Assessment)and highlights their reliance on specific data and perspectives.It emphasizes the growing importance of on-site monitoring with mid-IR technology.Additionally,it underscores the potential of aircraft-based and satellite remote sensing for comprehensive N_(2)O emissions data.The reviewalso highlights recent advancements in emission mitigation,particularly in adipic acid synthesis techniques,showing substantial potential for N_(2)O reduction.Innovative paradigms and strategies for N_(2)O mitigation in the adipic acid industry are presented,with a focus on achieving nitrogen oxides(NO_(x))-free production.These approaches hold promise for emission reduction,given the high removal efficiency in plant end-of-treatment processes.Various accounting methods,monitoring techniques,and mitigation strategies were integrated and analyzed to provides a comprehensive overview of N_(2)O emissions in the adipic acid industry,with the aim of guiding future research and policy initiatives.展开更多
The direct oxidation of cyclohexane to adipic acid(AA)without the use of HNO_(3)is important but still challenging.Herein,hierarchical manganese-containing TS-1 zeolite(HMTS)was prepared using an improved direct synth...The direct oxidation of cyclohexane to adipic acid(AA)without the use of HNO_(3)is important but still challenging.Herein,hierarchical manganese-containing TS-1 zeolite(HMTS)was prepared using an improved direct synthesis method,in which titanium and manganese coexist within the zeolite matrix,as characterized by X-ray diffraction,X-ray photoelectron spectroscopy,transmission electron microscopy,ultraviolet,extended X-ray absorption fine structure etc.The introduction of matrix Mn species(Mn^(3+),Mn^(4+))not only increased the surface oxygen vacancies,but also generated medium-strong acid sites,which endowed HMTS catalysts with the ability to efficiently activate oxygen and facilitate substrate coordination.On HMTS-3,one-pot oxidation of cyclohexane at 140℃and 2 MPa O_(2)gave 81.6%conversion and 71.5%AA selectivity,the highest value obtained at present.Control experiments with single-component samples confirmed that matrix Ti^(4+)catalyzed the conversion of cyclohexane to a mixture of cyclohexanone and cyclohexanol(KA oil),and matrix Mn favored the conversion of KA oil to AA.The synergy between matrix Ti and Mn inside the hierarchical structure were the key factor for the superior activity.Specifically,the matrix Ti^(4+)might activate oxygen to form Ti-O_(2)2-which facilitated the activation of the C-H bond of cyclohexane.The activation of O_(2)on matrix Mn^(3+)formed Mn^(4+)-O_(2)-favoring the breaking of the C-C bond of cyclohexanone.The hierarchical structure not only exposed more active sites and promoted mass transfer,but also provided a better microenvironment for the matrix Mn to synergize with the matrix Ti,which facilitated the overall reaction.This work demonstrated the practical application potential of HMTS and provided useful insights into the direct oxidation of cyclohexane to AA.展开更多
Constructing electrocatalytic overall reaction technology to couple the electrosynthesis of adipic acid with energy-saving hydrogen production is of significant for sustainable energy systems.However,the development o...Constructing electrocatalytic overall reaction technology to couple the electrosynthesis of adipic acid with energy-saving hydrogen production is of significant for sustainable energy systems.However,the development of highly-active bifunctional electrocatalysts remains a challenge.Herein,3D hierarchical nickel-copper alloying arrays with dendritic morphology are manufactured by a simple electrodeposition process,standing for the excellent bifunctional electrocatalyst towards the co-production of adipic acid and H_(2)from cyclohexanone and water.The membrane-free flow electrolyzer of Cu_(0.81)Ni_(0.19)/NF shows the superior electrooxidation performance of ketone-alcohol(KA)oil with high faradaic efficiencies of over 90%for adipic acid and H_(2),robust stability over 200 h as well as a high yield of 0.6 mmol h^(-1) for adipic acid at 100 mA cm^(-2).In-situ spectroscopy indicates the Cu_(0.81)Ni_(0.19)alloy contributes to forming more active NiOOH species to involve in the conversion of cyclohexanone to adipic acid,while the proposed reaction pathway undergoes the 2-hydroxycyclohexanone and 2,7-oxepanedione intermediates.Moreover,the theoretical calculations confirm that the optimal electronic interaction,boosted reaction kinetics as well as improved adsorption free energy of reaction intermediates,synergistically endows Cu_(0.81)Ni_(0.19)alloy with superior bifunctional performance.展开更多
An aliphatic polyester, poly(hexalene adipate) (PHA) and an aliphatic copolyester, poly (hexalene adipate succinate) (PHAS) were synthesized by direct condensation of corresponding binary acid and binary alcohol in th...An aliphatic polyester, poly(hexalene adipate) (PHA) and an aliphatic copolyester, poly (hexalene adipate succinate) (PHAS) were synthesized by direct condensation of corresponding binary acid and binary alcohol in the presence of a catalyst, p-toluene sulfonic acid. The biodegradation of these polyesters were studied in the laboratory by enzyme attack and outdoor soil burial. The results show that these polyesters have good biodegradability and the copolyester PHAS, even displayed a better biodegradability than the polyester PHA. In the presence of Penicillium chrysogenum the weight loss reached 18.3% for the PHAS (film thickness 1.0 mm) and 9.1% for the PHA (film thickness 1.0 mm) after 28 days. Outdoor soil burial tests indicate that these polyesters also have good biodegradability in natural conditions. The weight loss reached 14.2% for PHAS (film thickness 0.1 mm) and 6.7% for PHA (film thickness 0.1 mm) after burying in soil for 36 days.展开更多
The influence of adipic acid on the formation and corrosion resistance of anodic oxide film fabricated on 2024 aluminum alloy was investigated. The morphology was investigated by scanning electron microscopy （SEM） a...The influence of adipic acid on the formation and corrosion resistance of anodic oxide film fabricated on 2024 aluminum alloy was investigated. The morphology was investigated by scanning electron microscopy （SEM） and transmission electron microscopy （TEM）, respectively. The corrosion resistance was evaluated by electrochemical impedance spectroscopy （EIS）. The results showed that the adipic acid was absorbed at the electrolyte/anodic layer interface during anodizing. The corrosion rate of anodic film decreased and the film thickness increased. The film was uniform and compact especially at the film/substrate interface. After sealing procedure, anodic film formed with the addition of adipic acid exhibited improved dielectric property and corrosion resistance in aggressive environment.展开更多
Based on the kinetic and thermodynamic equations, a comprehensive mathematical model for the con- tinuous esterification process of polyester polyols was developed, which was carried out in an innovational bub- bling ...Based on the kinetic and thermodynamic equations, a comprehensive mathematical model for the con- tinuous esterification process of polyester polyols was developed, which was carried out in an innovational bub- bling reactive distillation tower （BRDT） at atmospheric pressure. In this new type of reactor, direct esterification between ethylene glycol and adipic acid was accomplished efficiently and rapidly. A bench BRDT with the height of 2 m was applied for the esteriflcation process of l^oly （ethylene adlpate） （P＇EA）. In the continuous operation, Hn- ear oligomers were discharged from the bottom of the column, while water passed a few column trays and a pack- ing section as a condensation byproduct. The influence of major operating conditions on reactor performance was also simulated. Simulation results were in good agreement with experimental data, providing a strategy for devel- oping and optimizing this process.展开更多
The enzyme-mediated highly enantioselective hydrolysis of aliphatic dicarboxylic acid diesters has been developed. The racemic diesters were easily prepared by the coupling of racemic alcohols with dicarboxylic anhydr...The enzyme-mediated highly enantioselective hydrolysis of aliphatic dicarboxylic acid diesters has been developed. The racemic diesters were easily prepared by the coupling of racemic alcohols with dicarboxylic anhydrides followed by esterification or with dicarboxylic acids. In the cases of bis(1-phenylethyl) glutarate and bis(1-phenylethyl) adipate, the diesters which contained the dl- and meso-form diastereomers, were enantioselectively hydrolyzed by lipase from Candida antarctica (Novozym 435) in buffer at 30°C to afford the almost optically pure (R)-1-phenylethanol. On the other hand, the following chemical hydrolysis of the remaining (S, S)-diesters and (S)-monoesters gave the (S)-alcohol. Finally, both enantiomers were stoichiometrically obtained in about 100% isolated yield based on the racemic diesters. The enzymatic reaction was also applicable for the preparation of several optically active alcohols. In some cases, both the reactivities and enantioselectivities were quite different from those in the case of the corresponding simple acetates.展开更多
基金financially supported by the National Natural Science Foundation of China(No.21304070)Natural Science Foundation of Tianjin City(No.15JCYBJC47300)+1 种基金Major Program of National Natural Science Foundation of China(No.11432016)the Municipal Key Program of Natural Science Foundation of Tianjin(No.14JCZDJC40700)
文摘Zinc phenylphosphonate （PPZn）, a benign and biocompatible nucleating agent, was prepared and incorporated into the biodegradable poly（ethylene adipate） （PEA） to investigate its effect on the crystallization behavior, crystallization kinetics and spherulite morphology of PEA. Upon addition of PPZn, the crystallization temperature and crystallinity of PEA in the non-isothermal crystallization process increased significantly. Analysis of crystallization kinetics by Avrami equation suggests that the crystallization time shortened greatly and crystallization rate increased markedly after addition of PPZn. In the presence of PPZn, the spherulite size decreased and spherulite density increased significantly. It suggests that PPZn is an efficient nucleating agent for the crystallization of PEA. The accelerated crystallization in the presence of PPZn is mainly attributed to the epitaxial nucleation of PEA crystals on the surface of PPZn crystals, that is, a perfect lattice matching between PEA crystal and PPZn crystal occurs.
基金financially supported by the National Natural Science Foundation of China(Nos.21204045 and 21276151)Natural Science Basic Research Plan in Shaanxi Province of China(No.2011JQ2004)Key Scientific Research Group of Shaanxi Province(No.2013KCT-08)
文摘The effects of crystallization temperature and blend ratio on the polymorphic crystal structures of poly（butylene adipate） （PBA） in poly（butylene succinate） （PBS）/poly（butylene adipate） （PBS/PBA） blends were studied by means of differential scanning calorimetry （DSC）, wide-angle X-ray diffraction （XRD） and atomic force microscopy （AFM）. It was revealed that the polymorphism of PBA can be regulated by the blend ratio even in a non-isothermal crystallization process. The results demonstrate that high temperature favors fiat-on α crystals, while low temperature contributes to edge-on β crystals. It was also found that the effect of blend ratio on the crystallization mechanism of PBA is well coincident with that of the crystallization temperature. The increment of PBS content in the PBS/PBA blend gives rise to more β-form crystals of PBA. For those PBS/PBA blends with low PBA content, the interlamellar phase segregation of PBA makes its molecular chains so difficult to diffuse from one isolated microdomain to another that high crystallization temperature and sufficiently long crystallization time will be required if the PBA α-type crystals are targeted.
基金financially supported by the National Natural Science Foundation of China(Nos.50833006,21274009,21204018,51221002and50973008)
文摘The crystallization behavior of poly（ethylene adipate） （PEA） on highly oriented high-density polyethylene （PE） substrate both from solution and isotropic melt was studied by means of optical microscopy, differential scanning calorimetry, atomic force microscopy and electron diffraction. The results show that the PE influences the crystallization of PEA strongly, which results in an epitaxial growth of PEA with well ordered structure. At the boundary of the PE substrate, a transcrystalline PEA layer is observed. Fine structural observation illustrates that the PEA grows on the PE substrate in edge- on lamellae with fixed orientation. Electron diffraction demonstrates that the epitaxial organization of PEA on PE occurs with both polymer chains parallel, which leads to the （00l） PEA diffractions inclined ±23.5° to the chain direction of PE crystals. Combining the real space morphological observation and electron diffraction results, it is concluded that the epitaxial PEA edge-on lamellae are folded in the {00l} lattice planes.
基金financially supported by the National Natural Science Foundation of China(Nos.21204045,21276151)Key Scientific Research Group of Shanxi Province(No.2013KCT-08)Scientific Research Group of Shanxi University of Science and Technology(No.TD12-04)
文摘The miscibility, isothermal crystallization kinetics and morphology of the poly（vinylidene fluoride）（PVDF）/poly（ethylene adipate）（PEA） blends have been studied by differential scanning calorimetry（DSC）, optical microscopy（OM） and scanning electron microscopy（SEM）. A depression of the equilibrium melting point of PVDF was observed. From the melting point data of PVDF, a negative but quite small value of the interaction parameter ？PVDF-PEA is derived using the Flory-Huggins equation, implying that PVDF shows miscibility with PEA to some extent. Nonisothermal and isothermal crystallization kinetics suggest that the crystallization rate of PVDF decreases with increasing the amount of PEA, and a contrary trend was found when PEA crystallizes with the increase of the amount of PVDF. It was further disclosed that the blend ratio and crystallization temperature affect the texture of PVDF spherulites greatly, which determines the subsequent crystallization of PEA. At high temperatures, e.g. 150 ℃, the band spacing of PVDF spherulites increases with the addition of PEA content and the spherulitic structure becomes more open. In this case, spherulitic crystallization of PEA is not observed for all blend compositions. At low temperatures, e.g. 130 ℃, for the PEA-rich blends, the interpenetrated structures are eventually formed by the penetration of the spherulites of PEA growing within the pre-existing PVDF spherulites.
基金financially supported by the National Natural Science Foundation of China(No.51025314)the Oticon Foundation in Denmark
文摘Oriented and non-oriented Teflon films, which were found to have the same crystalline structure, but different surface morphologies, were used to sandwich poly（butylene adipate） （PBA） films during isothermal crystallization. It was found that both the Teflon surface structure and the PBA polymorphic structure are the determining factors to induce epitaxial crystallization. The oriented Teflon film was able to induce epitaxial crystallization of PBA α crystal, while the non-oriented Teflon did not induce any epitaxial crystallization of PBA. Epitaxial crystallization did not occurred for PBA β crystals between neither the oriented nor the non-oriented Teflon films. The enzymatic degradation rate of PBA films was not determined by the epitaxial crystallization, in fact it was still dependent on the polymorphic crystal structure of PBA. The morphological changes of PBA films after enzymatic degradation confirmed again that the epitaxial crystallization only occurred for the PBA film with α crystal structure which was produced by being sandwiched between oriented Teflon films, and it happened only on the surface of PBA films.
基金financially supported by the National Natural Science Foundation of China(Nos.21204045 and 21276151)Key Scientific Research Group of Shanxi Province(No.2013KCT-08)Scientific Research Group of Shanxi University of Science and Technology(No.TD12-04)
文摘The effects of PEA on the ）γ-phase PVDF crystal structure and the crystallization of PEA within the pre-existing γ-phase PVDF spherulites have been investigated by optical microscopy （OM）, infrared spectroscopy （IR） and scanning electron microscopy （SEM）. The results demonstrate that the γ-phase PVDF spherulites consist of the lamellae exhibiting a highly curved scroll-like morphology and develop preferentially in PEA-rich blend. With increasing PEA concentration, the scroll diameter increases and the scrolls are better separated from each other. PEA crystallizes first in the interspherulitic region and transcrystalline layer develops. Subsequently, the transcrystalline layer of PEA continues to grow within theγ-phase PVDF spherulites, e.g., in the region between the scrolls, until impinging on other PEA transcrystalline layers or spherulites. The crystallization kinetics results indicate that the growth rate of PEA crystals in the intraspherulitic region of γ-phase PVDF shows a positive correlation with content of PEA, but a negative one with the crystallization temperature of γ-phase PVDF.
基金the National Key Research and Development Program of China(No.2022YFB3704900)the National Natural Science Foundation of China(No.52073004)China National Tobacco Corporation Guizhou Company(No.2023XM24)。
文摘Poly(glycolic acid)(PGA)is derived from glycolide obtained by fermenting pineapples or sugarcane,which has excellent gas barrier properties and a small carbon footprint.PGA is a potential substitute for the current aluminum-plastic composite films used in high barrier packaging applications.However,its poor ductility and narrow processing window limit its application in food packaging.Herein,poly(butylene succinate-co-butylene adipate)(PBSA)was used to fabricate PGA/PBSA blend films through an in situ fibrillation technique and blown film extrusion.Under the elongational flow field used during the extrusion process,a unique hierarchical structure based on the PBSA nanofibrils and interfacially oriented PGA crystals was obtained.This structure enhances the strength,ductility and gas barrier properties of the PGA/PBSA blend film.In addition,an epoxy chain extender(ADR4468)was used as a compatibilizer to further enhance the interfacial adhesion between PGA and PBSA.70PGA/0.7ADR exhibited a very low oxygen permeability(2.34×10^(-4)Barrer)with significantly high elongating at break(604.4%),tensile strength(47.4 MPa),and transparency,which were superior to those of petroleum-based polymers.Thus,the 70PGA/0.7ADR blown films could satisfy the requirements for most instant foods such as coffee,peanuts,and fresh meat.
文摘In the present study,thermal behavior and crystal transition of pure poly(butylene adipate)(PBA)upon heating process were investigated by FTIR spectroscopy.To gain further insight into the thermal behavior alteration and the phase transition of PBA,we performed two-dimensional(2D)correlation analysis.We found thatβ-form PBA crystal undergoes not only the melting process but also crystal transition upon the heating process.
基金financially supported by the National Natural Science Foundation of China(No.21674128)China University of Petroleum(Beijing)
文摘We successfully use a co-precipitation method to prepare inclusion complex between poly（butylene adipate） （PBA） chains （vip component） and urea molecules （host component）. The PBA/urea inclusion complex is confirmed to adopt a hexagonal crystal modification with lattice parameters ofa = 8.14 A and c = 10.92 A, and the interaction between PBA chains and urea is van der Waals force. The singly isolated PBA chains are suggested to take some gauche conformation, which is different from the all-trans conformation in r-form PBA. Furthermore, we employ the isolated PBA chains which are uniformly pre-established in a specific conformation in urea channels to regulate the crystal form of PBA for the first time. After removing the host urea molecules, the coalesced PBA chains are found to solely crystallize into a-form crystals at different coalescing temperatures. By comparing the FTIR spectra, it is found that PBA chains in inclusion complex plausibly contain some similar conformers as those in a-form crystal, which is suggested to be the intrinsic reason for the sole formation of a-form crystals. This research proves that inclusion complex can be used as a very effective method to regulate polymorphism of semi-crystalline polymers.
基金The authors are grateful for the financial support from the National Basic Research Program of China，the National Natural Science Foundation of China
文摘The ester base oil of dioctyl adipate (DOA) was oxidized in an oven at 200 degrees C for 30 h, and variations in the physicochemical and tribological properties were studied. To investigate the thermal-oxidation mechanism, the thermal-oxidation products were analyzed by gas chromatography-mass spectrometry (GC-MS), and the thermal-oxidation process was simulated using visual reactive force field molecular dynamics (ReaxFF MD). The results indicated that the total acid number (TAN) increased significantly because of the presence of 14% carboxylic acids and low molecular weight monoesters. The tribological properties were improved by the formation of the strongly polar carboxylic acids. Additionally, the increase in kinematic viscosity was limited due to the formation of high molecular weight polymerization products and low molecular weight degradation products. Thermal-oxidative degradation and polymerization mechanisms were proposed by combining ReaxFF MD simulations and GC-MS results.
基金supported by the Zhangjiang Science and Technology Development Foundation of Guangdong,China (2009C3101015)Doctoral Starting Foundation of Guangdong Medical College (XB0811)
文摘A facile route for the synthesis of dimethyl adipate （DAP） from cyclopentanone and dimethyl carbonate （DMC） in the pres- ence of solid base catalysts has been developed. It was found that the intermediate carbomethoxycyclopentanone （CMCP） was produced from cyclopentanone with DMC in the first step, and then CMCP was further converted to DAP by reacting with a methoxide group. The role of the basic catalysts can be mainly ascribed to the activation of cyclopentanone via the abstraction of a proton in the a-position by base sites, and solid bases with moderate strength, such as MgO, favor the formation of DAP.
基金Financial support from National Natural Science Foundation of China(Grant No.22075298)National Key R&D Program of China(2022YFD2301204)is gratefully acknowledged.
文摘In this manuscript,we conveniently prepared a series of polyester-polycarbonate copolymer(PPC-P)/polybutylene adipate terephthalate(PBAT)blends that exhibit both flame-retardant properties and toughness.Piperazine pyrophosphate(PAPP),melamine phosphate(MPP)and ZnO were used as synergistic flame retardants for PPC-P/PBAT blends.The effects of synergistic flame retardants on thermal stability,combustion behavior and flame retardancy of PPC-P/PBAT blends were investigated.The results showed that when the ratio of PAPP/MPP/ZnO was 18.4:9.2:2.4,the LOI of PPC-P/PBAT composite was 42.8%,and UL-94 reached V-0 level.The results of cone calorimetry showed that the mass loss rate(MLR),the peak value of the biggest smoke production rate(pSPR)and total smoke production(TSP)of the material decreased,and a continuously expanded carbon layer with a compact structure was formed after combustion.The carbon layer formed after surface combustion protects the material from decomposition over a long temperature range.In terms of mechanical properties,compared with the composites with only PAPP and MPP,PAPP/MPP/ZnO composites can improve the mechanical properties.After adding 2.4 wt% ZnO,the tensile strength and impact strength of the polymer increased to 34.2 MPa and 28.5 kJ/m^(2),respectively.The results showed that the use of non-toxic,environmentally friendly,halogen-free flame retardants to enhance the flame retardant properties of biodegradable polymer composites is a promising direction in the future.
基金supported by the National Key R&D Program of China(No.2023YFC3707201)the National Natural Science Foundation of China(No.52320105003)+1 种基金the Informatization Plan of Chinese Academy of Sciences(No.CAS-WX2023PY-0103)the Fundamental Research Funds for the Central Universities(No.E3ET1803).
文摘Nitrous oxide(N_(2)O),as an important gas affecting climate warming,is attracting attention from allwalks of life.This reviewaddresses N_(2)O emissions status in the adipic acid industry,a significant industrial greenhouse gas source.It elucidates the N_(2)O emission mechanism and influencing factors in adipic acid production.It extensively evaluates N_(2)O emission accounting methods,including Intergovernmental Panel on Climate Change(IPCC)Guidelines,World Resources Institute(WRI)Protocol,and others.While the IPCC emission factor method offers simplicity and comparability,it may lack precision for facilities with advanced emission reduction measures.To address this,a combined modeling and monitoring approach is advocated.It scrutinizes modeling methods(statistical techniques,Greenhouse Gas and Air Pollution Interactions and Synergies,and Life-cycle Assessment)and highlights their reliance on specific data and perspectives.It emphasizes the growing importance of on-site monitoring with mid-IR technology.Additionally,it underscores the potential of aircraft-based and satellite remote sensing for comprehensive N_(2)O emissions data.The reviewalso highlights recent advancements in emission mitigation,particularly in adipic acid synthesis techniques,showing substantial potential for N_(2)O reduction.Innovative paradigms and strategies for N_(2)O mitigation in the adipic acid industry are presented,with a focus on achieving nitrogen oxides(NO_(x))-free production.These approaches hold promise for emission reduction,given the high removal efficiency in plant end-of-treatment processes.Various accounting methods,monitoring techniques,and mitigation strategies were integrated and analyzed to provides a comprehensive overview of N_(2)O emissions in the adipic acid industry,with the aim of guiding future research and policy initiatives.
文摘The direct oxidation of cyclohexane to adipic acid(AA)without the use of HNO_(3)is important but still challenging.Herein,hierarchical manganese-containing TS-1 zeolite(HMTS)was prepared using an improved direct synthesis method,in which titanium and manganese coexist within the zeolite matrix,as characterized by X-ray diffraction,X-ray photoelectron spectroscopy,transmission electron microscopy,ultraviolet,extended X-ray absorption fine structure etc.The introduction of matrix Mn species(Mn^(3+),Mn^(4+))not only increased the surface oxygen vacancies,but also generated medium-strong acid sites,which endowed HMTS catalysts with the ability to efficiently activate oxygen and facilitate substrate coordination.On HMTS-3,one-pot oxidation of cyclohexane at 140℃and 2 MPa O_(2)gave 81.6%conversion and 71.5%AA selectivity,the highest value obtained at present.Control experiments with single-component samples confirmed that matrix Ti^(4+)catalyzed the conversion of cyclohexane to a mixture of cyclohexanone and cyclohexanol(KA oil),and matrix Mn favored the conversion of KA oil to AA.The synergy between matrix Ti and Mn inside the hierarchical structure were the key factor for the superior activity.Specifically,the matrix Ti^(4+)might activate oxygen to form Ti-O_(2)2-which facilitated the activation of the C-H bond of cyclohexane.The activation of O_(2)on matrix Mn^(3+)formed Mn^(4+)-O_(2)-favoring the breaking of the C-C bond of cyclohexanone.The hierarchical structure not only exposed more active sites and promoted mass transfer,but also provided a better microenvironment for the matrix Mn to synergize with the matrix Ti,which facilitated the overall reaction.This work demonstrated the practical application potential of HMTS and provided useful insights into the direct oxidation of cyclohexane to AA.
基金financially supported by the National Natural Science Foundation of China(22205205,22472151)the Zhejiang Provincial Natural Science Foundation of China(LQ22B030008)the Science Foundation of Zhejiang Sci-Tech University(ZSTU)under Grant No.21062337-Y.
文摘Constructing electrocatalytic overall reaction technology to couple the electrosynthesis of adipic acid with energy-saving hydrogen production is of significant for sustainable energy systems.However,the development of highly-active bifunctional electrocatalysts remains a challenge.Herein,3D hierarchical nickel-copper alloying arrays with dendritic morphology are manufactured by a simple electrodeposition process,standing for the excellent bifunctional electrocatalyst towards the co-production of adipic acid and H_(2)from cyclohexanone and water.The membrane-free flow electrolyzer of Cu_(0.81)Ni_(0.19)/NF shows the superior electrooxidation performance of ketone-alcohol(KA)oil with high faradaic efficiencies of over 90%for adipic acid and H_(2),robust stability over 200 h as well as a high yield of 0.6 mmol h^(-1) for adipic acid at 100 mA cm^(-2).In-situ spectroscopy indicates the Cu_(0.81)Ni_(0.19)alloy contributes to forming more active NiOOH species to involve in the conversion of cyclohexanone to adipic acid,while the proposed reaction pathway undergoes the 2-hydroxycyclohexanone and 2,7-oxepanedione intermediates.Moreover,the theoretical calculations confirm that the optimal electronic interaction,boosted reaction kinetics as well as improved adsorption free energy of reaction intermediates,synergistically endows Cu_(0.81)Ni_(0.19)alloy with superior bifunctional performance.
文摘An aliphatic polyester, poly(hexalene adipate) (PHA) and an aliphatic copolyester, poly (hexalene adipate succinate) (PHAS) were synthesized by direct condensation of corresponding binary acid and binary alcohol in the presence of a catalyst, p-toluene sulfonic acid. The biodegradation of these polyesters were studied in the laboratory by enzyme attack and outdoor soil burial. The results show that these polyesters have good biodegradability and the copolyester PHAS, even displayed a better biodegradability than the polyester PHA. In the presence of Penicillium chrysogenum the weight loss reached 18.3% for the PHAS (film thickness 1.0 mm) and 9.1% for the PHA (film thickness 1.0 mm) after 28 days. Outdoor soil burial tests indicate that these polyesters also have good biodegradability in natural conditions. The weight loss reached 14.2% for PHAS (film thickness 0.1 mm) and 6.7% for PHA (film thickness 0.1 mm) after burying in soil for 36 days.
基金Project(51271012)supported by the National Natural Science Foundation of China
文摘The influence of adipic acid on the formation and corrosion resistance of anodic oxide film fabricated on 2024 aluminum alloy was investigated. The morphology was investigated by scanning electron microscopy （SEM） and transmission electron microscopy （TEM）, respectively. The corrosion resistance was evaluated by electrochemical impedance spectroscopy （EIS）. The results showed that the adipic acid was absorbed at the electrolyte/anodic layer interface during anodizing. The corrosion rate of anodic film decreased and the film thickness increased. The film was uniform and compact especially at the film/substrate interface. After sealing procedure, anodic film formed with the addition of adipic acid exhibited improved dielectric property and corrosion resistance in aggressive environment.
基金Supported by the National Natural Science Foundation of China （21176070）.
文摘Based on the kinetic and thermodynamic equations, a comprehensive mathematical model for the con- tinuous esterification process of polyester polyols was developed, which was carried out in an innovational bub- bling reactive distillation tower （BRDT） at atmospheric pressure. In this new type of reactor, direct esterification between ethylene glycol and adipic acid was accomplished efficiently and rapidly. A bench BRDT with the height of 2 m was applied for the esteriflcation process of l^oly （ethylene adlpate） （P＇EA）. In the continuous operation, Hn- ear oligomers were discharged from the bottom of the column, while water passed a few column trays and a pack- ing section as a condensation byproduct. The influence of major operating conditions on reactor performance was also simulated. Simulation results were in good agreement with experimental data, providing a strategy for devel- oping and optimizing this process.
文摘The enzyme-mediated highly enantioselective hydrolysis of aliphatic dicarboxylic acid diesters has been developed. The racemic diesters were easily prepared by the coupling of racemic alcohols with dicarboxylic anhydrides followed by esterification or with dicarboxylic acids. In the cases of bis(1-phenylethyl) glutarate and bis(1-phenylethyl) adipate, the diesters which contained the dl- and meso-form diastereomers, were enantioselectively hydrolyzed by lipase from Candida antarctica (Novozym 435) in buffer at 30°C to afford the almost optically pure (R)-1-phenylethanol. On the other hand, the following chemical hydrolysis of the remaining (S, S)-diesters and (S)-monoesters gave the (S)-alcohol. Finally, both enantiomers were stoichiometrically obtained in about 100% isolated yield based on the racemic diesters. The enzymatic reaction was also applicable for the preparation of several optically active alcohols. In some cases, both the reactivities and enantioselectivities were quite different from those in the case of the corresponding simple acetates.
