In this paper, acrylonitrile-butadiene-styrene （ABS） nanocomposite foams are produced using carbon dioxide through the solid-state batch process. Microcellular closed-cell foams are produced with the relative densit...In this paper, acrylonitrile-butadiene-styrene （ABS） nanocomposite foams are produced using carbon dioxide through the solid-state batch process. Microcellular closed-cell foams are produced with the relative density ranging from 0.38 to 0.97. The effects of the processing conditions on the density, morphology, and flexural properties of ABS and its nanocomposite foams are studied. It is found that nanoclay particles, as nucleating sites, play an important role in reducing the size of cells and increasing their number in the unit volume of foamed polymer, as well as increasing the flexural modulus of foam through reinforcing its matrix.展开更多
Palygorskite （PGS） and vinyl tris-（2-methoxyethoxy） silane （KH-172） modified palygorskite （OPGS） were used to prepare acrylonitrile-butadiene-styrene （ABS）/clay composites. Thermal stability of the composite...Palygorskite （PGS） and vinyl tris-（2-methoxyethoxy） silane （KH-172） modified palygorskite （OPGS） were used to prepare acrylonitrile-butadiene-styrene （ABS）/clay composites. Thermal stability of the composites was evaluated by using thermogravimetric analysis （TGA）. The morphology of the fractured surface and the degree of dispersion of the clay in the ABS matrix were observed by scanning electron microscopy （SEM）. X-ray diffraction （XRD） analysis results showed the variation of the crystal structure. Measurements of the tensile properties of the ABS/clay composites proved that the ABS/OPGS composited material represented the most excellent tensile property, because of good compatibility and dispersion of ABS with OPGS.展开更多
The theory of chemical shift effect of substituent was applied to the assignment of the 13 C NMR spectra of the ethylene/propylene and ethylene/octene 1 copolymers. Using the parameters derived above a...The theory of chemical shift effect of substituent was applied to the assignment of the 13 C NMR spectra of the ethylene/propylene and ethylene/octene 1 copolymers. Using the parameters derived above and the DEPT technique, we then entirely assigned the 13 C NMR spectra of the ethylene/propylene/octene 1 terpolymers synthesized in the presence of the same heterogeneous supported Ziegler Natta catalyst, TiCl 4/MgCl 2/ i Bu 3Al. The present paper also covers the terpolymer composition and the monomer sequence distributions of a series of ethylene/propylene/octene 1 terpolymers.展开更多
Scavenging abilities of the ethylenediamine, diethylenetriamine and tris(2-aminoethyl)amine functionalized resins derived from the low cross-linked glycidyl methacrylate-styrene gels in relation to the selected transi...Scavenging abilities of the ethylenediamine, diethylenetriamine and tris(2-aminoethyl)amine functionalized resins derived from the low cross-linked glycidyl methacrylate-styrene gels in relation to the selected transition metal ions and organic (acid chlorides) electrophiles were explored. The synergetic effects of the solvents were found for the metal ion uptake. In this case a pair of solvents capable simultaneously to swell the hydrophobic core of the resins and interact with the polar amine groups turned out to be a more effective medium for activation of the nucleophilic functionalities of the resins. The resin with ethylenediamine moieties proved to be effective in scavenging acyl chlorides from methylene chloride as well. However, it did not provide complete removing sulphonyl chlorides from the solutions. These organic electrophiles were removed effectively by the resins bearing tris(2-aminoethyl)amine functionalities.展开更多
This paper reports the phase separation behavior of ABS films cast on the surfaces of homopelymers or random copolymers.It is found that phase separation of ABS films was induced by the surfaces of the substrate polym...This paper reports the phase separation behavior of ABS films cast on the surfaces of homopelymers or random copolymers.It is found that phase separation of ABS films was induced by the surfaces of the substrate polymers.The relationship between the miscibility of the sub- strate polymers and the phase separation behavior of ABS films was also examined.展开更多
Compared to regular conjugated polymers,the random conjugated terpolymers are usually not beneficial to achieve highly efficient non-fullerene(NF)-based polymer solar cells(PSCs)due to their disordered chemical struct...Compared to regular conjugated polymers,the random conjugated terpolymers are usually not beneficial to achieve highly efficient non-fullerene(NF)-based polymer solar cells(PSCs)due to their disordered chemical structures.In this work,we report two random terpolymer donors(PBNB80 and PBNB50)by tuning the molar ratio of electron-accepting units of 1,3-di(thiophen-2-yl)naphtho[2,3-c]thiophene-4,9-dione(NTD)and 1,3-bis(4-chlorothiophen-2-yl)-4 H,8 H-benzo[1,2-c:4,5-c’]dithiophene-4,8-dione(ClBDD),at the same time,the parent polymers(PBNB100 and PBNB00)are also compared to study.These four polymer donors exhibit similar optical bandgaps and gradually deepen highest occupied molecular orbital levels.Importantly,aggregation and self-organization properties of the random terpolymer donors are optimized,which result in the better morphology and crystal coherence length after blending with NF acceptor of BO-4 Cl.Particularly,a PBNB80:BO-4 Cl blend forms an optimal nanoscale phase-separation morphology,thereby producing an outstanding power conversion efficiency of 16.0%,which is much higher than those(12.8%and 10.7%)of their parent binary polymer donor-based devices.This work demonstrates that rational using terpolymerization strategy to prepare random terpolymer is a very important method to achieve highly efficient NF-PSCs.展开更多
Synthesis of terpolymers consisting of two electron-donating monomers, viz. styrene and vinyl acetate with one electron-accepting monomer, i.e. acrylonitrile, initiated by p-nitrobenzyl triphenyl phosphonim ylide in d...Synthesis of terpolymers consisting of two electron-donating monomers, viz. styrene and vinyl acetate with one electron-accepting monomer, i.e. acrylonitrile, initiated by p-nitrobenzyl triphenyl phosphonim ylide in dioxane as diluent at 65°C for 150 min has been studied. The kinetic expression is Rpα[I]0.8[Sty] 1.2[VA] 1.4 [AN]1.2. The terpolymer composition was determined by the Kelen-Tüdos method. The values of reactivity ratios using r1 (Sty + VA) = 0.1 and r2 (AN) = 0.005. The overall activation energy is 46 kJ●mol●L–1. The formation of terpolymer is confirmed by the FTIR spectra showing bands at 3030 cm–1, 1598 cm–1, and 2362 cm–1, confirming the presence of phenyl, acetoxy and nitrile group respectively. The terpolymer has been characterized by 1H-Nuclear Magnetic Resonance, 13C-Nuclear Magnetic Resonance. The Differential Scanning Calorimetric curve shows the Tg of the polymer as 149.5°C. A scanning electron microscope confirms the polymer to be phosphorus free. Electron.Spin.Resonance spectra confirms phenyl radical responsible for initiation.展开更多
A novel surface modifying agent and internal compatilizer of inorganic and macromolecule composite materials,P(St/MAH/BA)terpolymer,was synthesized in butanone by solution polymerization method using styrene(St),malei...A novel surface modifying agent and internal compatilizer of inorganic and macromolecule composite materials,P(St/MAH/BA)terpolymer,was synthesized in butanone by solution polymerization method using styrene(St),maleic anhydride(MAH),and butyl acrylate(BA)as monomers and azobisisobutyronitrile(AIBN)as an initiator.Some affecting factors on terpolymers yields such as polymerization time,reaction temperature,solvent volume,initiator content,and reactants ratios were studied.Furthermore,the structure and thermal properties of terpolymers were primarily characterized and determined by Fourier Transform Infrared Spectroscopy(FTIR),nuclear magnetic resonance(NMR),thermogravimetric analysis(TGA),and gel permeation chromatography(GPC).The results indicate that the terpolymers are random polymers and the yields are low,but the thermal decomposed temperature of terpolymers P(St/MAH/BA)is around 220 ℃ and the average molecular weights(Mw)achieve 1.189×105 g·mol-1.展开更多
文摘In this paper, acrylonitrile-butadiene-styrene （ABS） nanocomposite foams are produced using carbon dioxide through the solid-state batch process. Microcellular closed-cell foams are produced with the relative density ranging from 0.38 to 0.97. The effects of the processing conditions on the density, morphology, and flexural properties of ABS and its nanocomposite foams are studied. It is found that nanoclay particles, as nucleating sites, play an important role in reducing the size of cells and increasing their number in the unit volume of foamed polymer, as well as increasing the flexural modulus of foam through reinforcing its matrix.
基金Funded by the National Natural Science Foundation of China (Nos.20674063 and 20774074)the Specialized Research Fund for the Doctoral Program of Higher Education (20050736001)
文摘Palygorskite （PGS） and vinyl tris-（2-methoxyethoxy） silane （KH-172） modified palygorskite （OPGS） were used to prepare acrylonitrile-butadiene-styrene （ABS）/clay composites. Thermal stability of the composites was evaluated by using thermogravimetric analysis （TGA）. The morphology of the fractured surface and the degree of dispersion of the clay in the ABS matrix were observed by scanning electron microscopy （SEM）. X-ray diffraction （XRD） analysis results showed the variation of the crystal structure. Measurements of the tensile properties of the ABS/clay composites proved that the ABS/OPGS composited material represented the most excellent tensile property, because of good compatibility and dispersion of ABS with OPGS.
基金Supported by the Foundation of Educational Ministry of China.
文摘The theory of chemical shift effect of substituent was applied to the assignment of the 13 C NMR spectra of the ethylene/propylene and ethylene/octene 1 copolymers. Using the parameters derived above and the DEPT technique, we then entirely assigned the 13 C NMR spectra of the ethylene/propylene/octene 1 terpolymers synthesized in the presence of the same heterogeneous supported Ziegler Natta catalyst, TiCl 4/MgCl 2/ i Bu 3Al. The present paper also covers the terpolymer composition and the monomer sequence distributions of a series of ethylene/propylene/octene 1 terpolymers.
文摘Scavenging abilities of the ethylenediamine, diethylenetriamine and tris(2-aminoethyl)amine functionalized resins derived from the low cross-linked glycidyl methacrylate-styrene gels in relation to the selected transition metal ions and organic (acid chlorides) electrophiles were explored. The synergetic effects of the solvents were found for the metal ion uptake. In this case a pair of solvents capable simultaneously to swell the hydrophobic core of the resins and interact with the polar amine groups turned out to be a more effective medium for activation of the nucleophilic functionalities of the resins. The resin with ethylenediamine moieties proved to be effective in scavenging acyl chlorides from methylene chloride as well. However, it did not provide complete removing sulphonyl chlorides from the solutions. These organic electrophiles were removed effectively by the resins bearing tris(2-aminoethyl)amine functionalities.
文摘This paper reports the phase separation behavior of ABS films cast on the surfaces of homopelymers or random copolymers.It is found that phase separation of ABS films was induced by the surfaces of the substrate polymers.The relationship between the miscibility of the sub- strate polymers and the phase separation behavior of ABS films was also examined.
基金the financial support from the National Natural Science Foundation of China(Grant Nos.51703228,51673201,21835006)Beijing National Laboratory for Molecular Sciences(BNLMS-CXXM-201903)。
文摘Compared to regular conjugated polymers,the random conjugated terpolymers are usually not beneficial to achieve highly efficient non-fullerene(NF)-based polymer solar cells(PSCs)due to their disordered chemical structures.In this work,we report two random terpolymer donors(PBNB80 and PBNB50)by tuning the molar ratio of electron-accepting units of 1,3-di(thiophen-2-yl)naphtho[2,3-c]thiophene-4,9-dione(NTD)and 1,3-bis(4-chlorothiophen-2-yl)-4 H,8 H-benzo[1,2-c:4,5-c’]dithiophene-4,8-dione(ClBDD),at the same time,the parent polymers(PBNB100 and PBNB00)are also compared to study.These four polymer donors exhibit similar optical bandgaps and gradually deepen highest occupied molecular orbital levels.Importantly,aggregation and self-organization properties of the random terpolymer donors are optimized,which result in the better morphology and crystal coherence length after blending with NF acceptor of BO-4 Cl.Particularly,a PBNB80:BO-4 Cl blend forms an optimal nanoscale phase-separation morphology,thereby producing an outstanding power conversion efficiency of 16.0%,which is much higher than those(12.8%and 10.7%)of their parent binary polymer donor-based devices.This work demonstrates that rational using terpolymerization strategy to prepare random terpolymer is a very important method to achieve highly efficient NF-PSCs.
文摘Synthesis of terpolymers consisting of two electron-donating monomers, viz. styrene and vinyl acetate with one electron-accepting monomer, i.e. acrylonitrile, initiated by p-nitrobenzyl triphenyl phosphonim ylide in dioxane as diluent at 65°C for 150 min has been studied. The kinetic expression is Rpα[I]0.8[Sty] 1.2[VA] 1.4 [AN]1.2. The terpolymer composition was determined by the Kelen-Tüdos method. The values of reactivity ratios using r1 (Sty + VA) = 0.1 and r2 (AN) = 0.005. The overall activation energy is 46 kJ●mol●L–1. The formation of terpolymer is confirmed by the FTIR spectra showing bands at 3030 cm–1, 1598 cm–1, and 2362 cm–1, confirming the presence of phenyl, acetoxy and nitrile group respectively. The terpolymer has been characterized by 1H-Nuclear Magnetic Resonance, 13C-Nuclear Magnetic Resonance. The Differential Scanning Calorimetric curve shows the Tg of the polymer as 149.5°C. A scanning electron microscope confirms the polymer to be phosphorus free. Electron.Spin.Resonance spectra confirms phenyl radical responsible for initiation.
基金Nano Project Foundation of Shanghai Technology Committee,China(No.0652nm039)Shanghai Leading Academic Discipline Project,China(No.B502)Shanghai Key Laboratory Proejct,China(No.08DZ2230500)
文摘A novel surface modifying agent and internal compatilizer of inorganic and macromolecule composite materials,P(St/MAH/BA)terpolymer,was synthesized in butanone by solution polymerization method using styrene(St),maleic anhydride(MAH),and butyl acrylate(BA)as monomers and azobisisobutyronitrile(AIBN)as an initiator.Some affecting factors on terpolymers yields such as polymerization time,reaction temperature,solvent volume,initiator content,and reactants ratios were studied.Furthermore,the structure and thermal properties of terpolymers were primarily characterized and determined by Fourier Transform Infrared Spectroscopy(FTIR),nuclear magnetic resonance(NMR),thermogravimetric analysis(TGA),and gel permeation chromatography(GPC).The results indicate that the terpolymers are random polymers and the yields are low,but the thermal decomposed temperature of terpolymers P(St/MAH/BA)is around 220 ℃ and the average molecular weights(Mw)achieve 1.189×105 g·mol-1.
