Annual production output of poly(ethylene terephthalate)(PET) fiber has been over 15 million tons in China due to its good mechanical properties and processability,but the shortage of hydrophilic group of PET has impo...Annual production output of poly(ethylene terephthalate)(PET) fiber has been over 15 million tons in China due to its good mechanical properties and processability,but the shortage of hydrophilic group of PET has imposed many limitations to further extend its application.The PET fabrics were grafted with polyacrylic acid in inverse microemulsion after low pressure plasma treatment,and the microstructure and properties of the grafted fabrics were investigated with infrared spectroscopy,scanning electron microscope(SEM),hydrophilic and mechanical tests.The grafting yield was increased with the grafting time.The grafting polymer was in the granular form with its particle size ranging from a few micrometers to a dozen of micrometers,normally smaller than the fiber diameter.The moisture regain and water uptake increased while the air permeability of the grafted fabrics decreased with the increase of grafting yield.The bending rigidity and tensile properties show slightly complicated behaviors with grafting yield.The inverse emulsion grafting technique can be used to control the grafting polymer architecture.展开更多
A new polymeric ionic liquid gel was prepared with 1-[(2-methacryloyloxy)ethyl]-3-methylimidazolium bromide(MEMImBr) via radiation-induced polymerization and cross-linking at room temperature.The resultant PMEMImBr ge...A new polymeric ionic liquid gel was prepared with 1-[(2-methacryloyloxy)ethyl]-3-methylimidazolium bromide(MEMImBr) via radiation-induced polymerization and cross-linking at room temperature.The resultant PMEMImBr gel exhibits high strength and flexibility as well as special swelling behavior in oil-in-water(O/W)emulsions.The swelling behavior of PMEMImBr gel in emulsions is similar to that in water except that the swelling rate in emulsions is slightly smaller than that in water.The organic solvents with higher polarity in the emulsions contribute to the swelling of PMEMImBr gels,and the O/W proportion of emulsion in the swollen gel equals approximately that of original emulsion when the concentration of organic solvent is lower than 0.2 g/g.展开更多
A poly(ethylene glycol) (PEG) based macroinitiator (MI) with terminal chloride atom at both ends was prepared by the reaction of PEG-400 with chloroacetyl chloride and used for the cationic polymerization of dodecyl v...A poly(ethylene glycol) (PEG) based macroinitiator (MI) with terminal chloride atom at both ends was prepared by the reaction of PEG-400 with chloroacetyl chloride and used for the cationic polymerization of dodecyl vinyl ether (DVE) yielding ABA type block copolymer. The block copolymer was then used as the surfactant for the emulsion polymerization of vinyl acetate and styrene in the presence of potassium persulfate as an initiator. The effects of new polymeric emulsifier on the physicochemical properties of obtained latexes were investigated depending on surfactant percentage in homopolymerizations.展开更多
Styrene-acrylate latex with high glass transition temperature （T）, low minimum film forming temperature（MFT） and good stability was prepared via core-shell emulsion polymerization. With semicontinuous process, hig...Styrene-acrylate latex with high glass transition temperature （T）, low minimum film forming temperature（MFT） and good stability was prepared via core-shell emulsion polymerization. With semicontinuous process, high conversion rate of monomer and low gel rate were achieved. The weight ratio of core monomer to shell monomer was approximately 1.35. It is found that many factors such as emulsifiers, initiators, reaction temperature, pH value and polymerization technology have influences on the permormance of styrene-acrylate latex. The prepared latex was characterized by TEM and FTIR. The obtained latex with T of 20.57 ℃, MFT or5.0 ℃, and good stability, had good stability of film forming.展开更多
Well-defined nonionic hydrophilic ω-acryloyl poly(ethylene oxide) macro-monomer (PEO-A) has been prepared by living anionic polymerization of ethylene oxidewith diphenyl methyl potassium as the initiator and acryloyl...Well-defined nonionic hydrophilic ω-acryloyl poly(ethylene oxide) macro-monomer (PEO-A) has been prepared by living anionic polymerization of ethylene oxidewith diphenyl methyl potassium as the initiator and acryloyl chloride as the reaction termi-nating agent. The polymer was characterized by FTIR and SEC. The emulsifier-free emul-sion polymerization of methyl methacrylate (MMA) and n-butyl acrylate (BA) containingvarious concentrations of PEO-A was studied. In all cases stable emulsion coplymerizationsof MMA and BA were obtained. The stabilizing effect was found to be dependent on themolecular weight and the feed amount of the macromonomer.展开更多
The emulsion polymerization of highly shear-stable copolymer dispersions of methyl methacrylate and butyl acrylate were carried out using poly （vinyl alcohol） with a thiol end group （PVA-SH） as protective colloid....The emulsion polymerization of highly shear-stable copolymer dispersions of methyl methacrylate and butyl acrylate were carried out using poly （vinyl alcohol） with a thiol end group （PVA-SH） as protective colloid. The dispersions can be transformed into corresponding redispersible powder via a spray dryingcooling process. On-line FT-IR monitoring shows that grafting polymer of PVA-g-PMMA was formed mainly at the stage-1 of the emulsion polymerization. TEM images show, the PVA-SH shell was fragmentary when adding SDS at initial stage and integrated when adding at particle growing or final stage. The particle size turns to be smaller when delayed adding SDS surfactant. Triethanolamine, a co-regulator of PVA-SH, controlled the M to 50 000-70 000 and reduced the PDI to 1.5-1.7. The acrylic dispersions with 0.8wt%-1.5wt% PVA-SH1 can be spray-dried into super dispersible polymer powder （SDPP）, which can easily disperse in water and form recon- stituted dispersions with an average particle size smaller than 1 micron.展开更多
Electrospun nanofibers present a new and rapidly growing research area due to their pronounced micro and nano characteristics associated with high surface area to volume ratio. Poly(styrene-co-acrylamide) and polystyr...Electrospun nanofibers present a new and rapidly growing research area due to their pronounced micro and nano characteristics associated with high surface area to volume ratio. Poly(styrene-co-acrylamide) and polystyrene polymers were synthesized by boiling temperature soap free emulsion polymerization in aqueous medium with potassium peroxosulphate as the initiator. The resulting polymers were dissolved in dimethylformamide and teterahydrofuran (DMF: THF) (4:1) to form polymer solutions that were electrospun into fiber mats with diameters ranging from 1.84 - 2.53 μm and 5.01 μm, respectively. The fibers were characterized by Fourier transform infrared spectroscopy (FTIR) equipped with universal ATR sampling accessory (4000 - 400 cm-1). The morphology and size were examined by a scanning electron miscroscope (SEM) and the thermal properties by thermogravimetric analysis (TGA). The FTIR spectra of the poly(styrene-co-acrylamide) revealed the presence of acrylamide on the polystyrene chain. Thus, surface modification of polystyrene with acrylamide is possible in a single step polymerization reaction prior to electrospinning.展开更多
Poly (acrylonitrile-co-vinyl acetate)/polypyrrole composite particles with uniform size and morphology have been synthesized using one-step polymerization that involves swelling and coating of polypyrrole (PPy) into P...Poly (acrylonitrile-co-vinyl acetate)/polypyrrole composite particles with uniform size and morphology have been synthesized using one-step polymerization that involves swelling and coating of polypyrrole (PPy) into P (AN-co-VAc) latex nanoparticles. As an initial stage, free radical copolymerization of acrylonitrile (AN) and vinyl acetate (VAc) was synthesized by emulsion polymerization using ammonium persulfate (APS) and dodecyl benzene sulfonic acid salt (DBSA) as a surfactant. P (AN-co-VAc)/PPy composites were obtained first time by in situ addition of the pyrrole into the reaction medium. The electrospun P (AN-co-VAc)/PPy nanofibers were obtained from the nanoparticles with better properties and the effect of PPy on the morphology of nanofibers was studied by scanning electron microscopy (SEM). High degree of homogeneity and molecular order induced by molecular dispersion of polypyrrole on copolymer matrix without phase separation improve the transport properties and stability of polypyrrole, which are critical for high-performance organic electronics.展开更多
This research investigates the formation of chitosan/poly （L-lactide） （CS/PLLA） porous composite scaffold using a novel emulsion freeze-drying technique. First, an oil in-water （O/W） emulsification system was us...This research investigates the formation of chitosan/poly （L-lactide） （CS/PLLA） porous composite scaffold using a novel emulsion freeze-drying technique. First, an oil in-water （O/W） emulsification system was used in the presence of surfactant Tween-80, in which CS solution was used as the water phase and PLLA solution was used as the oil phase. The emulsion was observed by inverted microscope （× 200）. The emulsion droplet was spherical and uniform in size. FT-IR analysis revealed that there were hydrogen bonding interactions between CS and PLLA components. The microstructure and physical properties of the scaffolds were also analyzed. The SEM results showed that composite scaffolds formed well interconnected pore structure and homogenous distribution of CS and PLLA. When the content of PLLA reached 50%, the porosity of CS/PLLA composite scaffolds were between 83 %-91% and density in the range of 0.047 to 0.11 g/era3. The porosity showed a slight decrease and the density increased with the increase of PLLA dose. The compressive strength increased from 0.32 to 0.43 MPa, while the compressive modulus increased from 1.99 to 3.91 MPa as the PLLA contents increased from 10% to 50%.展开更多
A series of well-defined core cross-linked star （CCS） polymeric ionic liquids （PILs） were synthesized via a three- step approach. First, the styrenic imidazole-based CCS polymer （S-PVBnIm） was prepared by the RA...A series of well-defined core cross-linked star （CCS） polymeric ionic liquids （PILs） were synthesized via a three- step approach. First, the styrenic imidazole-based CCS polymer （S-PVBnIm） was prepared by the RAFT-mediated heterogeneous polymerization in a water/ethanol solution, followed by the quaternization of S-PVBnIm with bromoalkanes and anion exchange. The CCS polymers were characterized by gel permeation chromatography （GPC）, nuclear magnetic resonance （NMR） spectroscopy, Fourier transform infrared spectroscopy （FTIR）, thermal gravimetric analysis （TGA）, and differential scanning calorimetry （DSC）. The obtained CCS polymers were used as the effective emulsifiers for oil-in-water high internal phase emulsions （HIPEs）. Multiple oils with different polarity including n-dodecane, undecanol, toluene and octanol were emulsified using 0.5 wt% S-PVBnIm aqueous solution under the acidic condition to form HIPEs with long-term stabilities. The excellent emulsification properties of CCS PILs were demonstrated by HIPE formation for a variety of oils. The properties of HIPEs in terms of emulsion type and oil droplet size were characterized by the confocal laser scanning microscopy （CLSM）. The intriguing capability of CCS PILs to stabilize HIPEs of various oils holds great potentials for the practical applications.展开更多
Submicron-sized P（St-NaSS） latexes were prepared via a semi-continuous emulsion copolymerization of styrene （St） and sodium styrene sulphonate （NaSS） in the presence of anionic surfactant, in which NaSS aqueous ...Submicron-sized P（St-NaSS） latexes were prepared via a semi-continuous emulsion copolymerization of styrene （St） and sodium styrene sulphonate （NaSS） in the presence of anionic surfactant, in which NaSS aqueous solution and St were separately dropwise charged into the polymerization system at the same time. The hydrodynamic diameter of the latex particles was measured by dynamic light scattering （DSL） method, and the NaSS unit content of the purified copolymer by water extraction was calculated based on the elementary analysis. Results showed that the copolymerization could be performed smoothly with the monomer conversion more than 96% in the absence of crosslinker, and PNaSS homopolymer could be removed from the latex product by water extraction for 28 h. The weight loss in the water extraction tended to decrease and the NaSS unit content of the purified copolymer tended to increase with the increase of monomer feeding time, and both of them increased with the increase of NaSS/St mole ratio in the charge. The introduction of divinyl benzene （DVB） could decrease the weight loss in the water extraction and increase the NaSS unit content of the purified copolymer. When 25/75 mole ratio of NaSS/St and 11 mol% DVB of total NaSS and St were used in the recipe, and the monomer feeding time was 3 h in copolymerization, the NaSS unit content of the purified copolymer reached 7.31 mol%.展开更多
基金the First Phase of Jiangsu Universities' Distinctive Discipline Development Program for Textile Science and Engineering of Soochow University,China
文摘Annual production output of poly(ethylene terephthalate)(PET) fiber has been over 15 million tons in China due to its good mechanical properties and processability,but the shortage of hydrophilic group of PET has imposed many limitations to further extend its application.The PET fabrics were grafted with polyacrylic acid in inverse microemulsion after low pressure plasma treatment,and the microstructure and properties of the grafted fabrics were investigated with infrared spectroscopy,scanning electron microscope(SEM),hydrophilic and mechanical tests.The grafting yield was increased with the grafting time.The grafting polymer was in the granular form with its particle size ranging from a few micrometers to a dozen of micrometers,normally smaller than the fiber diameter.The moisture regain and water uptake increased while the air permeability of the grafted fabrics decreased with the increase of grafting yield.The bending rigidity and tensile properties show slightly complicated behaviors with grafting yield.The inverse emulsion grafting technique can be used to control the grafting polymer architecture.
基金supported by the National Natural Science Foundation of China (No. 11375019)
文摘A new polymeric ionic liquid gel was prepared with 1-[(2-methacryloyloxy)ethyl]-3-methylimidazolium bromide(MEMImBr) via radiation-induced polymerization and cross-linking at room temperature.The resultant PMEMImBr gel exhibits high strength and flexibility as well as special swelling behavior in oil-in-water(O/W)emulsions.The swelling behavior of PMEMImBr gel in emulsions is similar to that in water except that the swelling rate in emulsions is slightly smaller than that in water.The organic solvents with higher polarity in the emulsions contribute to the swelling of PMEMImBr gels,and the O/W proportion of emulsion in the swollen gel equals approximately that of original emulsion when the concentration of organic solvent is lower than 0.2 g/g.
基金This work were supported by the Turkish Scientific and Technological Research Council(TUBITAK)(Project Number:108T722)Scientific Research Projects Coordination Center of Yildiz Technical University(Project Number:2012-01-02-KAP04).
文摘A poly(ethylene glycol) (PEG) based macroinitiator (MI) with terminal chloride atom at both ends was prepared by the reaction of PEG-400 with chloroacetyl chloride and used for the cationic polymerization of dodecyl vinyl ether (DVE) yielding ABA type block copolymer. The block copolymer was then used as the surfactant for the emulsion polymerization of vinyl acetate and styrene in the presence of potassium persulfate as an initiator. The effects of new polymeric emulsifier on the physicochemical properties of obtained latexes were investigated depending on surfactant percentage in homopolymerizations.
文摘Styrene-acrylate latex with high glass transition temperature （T）, low minimum film forming temperature（MFT） and good stability was prepared via core-shell emulsion polymerization. With semicontinuous process, high conversion rate of monomer and low gel rate were achieved. The weight ratio of core monomer to shell monomer was approximately 1.35. It is found that many factors such as emulsifiers, initiators, reaction temperature, pH value and polymerization technology have influences on the permormance of styrene-acrylate latex. The prepared latex was characterized by TEM and FTIR. The obtained latex with T of 20.57 ℃, MFT or5.0 ℃, and good stability, had good stability of film forming.
文摘Well-defined nonionic hydrophilic ω-acryloyl poly(ethylene oxide) macro-monomer (PEO-A) has been prepared by living anionic polymerization of ethylene oxidewith diphenyl methyl potassium as the initiator and acryloyl chloride as the reaction termi-nating agent. The polymer was characterized by FTIR and SEC. The emulsifier-free emul-sion polymerization of methyl methacrylate (MMA) and n-butyl acrylate (BA) containingvarious concentrations of PEO-A was studied. In all cases stable emulsion coplymerizationsof MMA and BA were obtained. The stabilizing effect was found to be dependent on themolecular weight and the feed amount of the macromonomer.
文摘The emulsion polymerization of highly shear-stable copolymer dispersions of methyl methacrylate and butyl acrylate were carried out using poly （vinyl alcohol） with a thiol end group （PVA-SH） as protective colloid. The dispersions can be transformed into corresponding redispersible powder via a spray dryingcooling process. On-line FT-IR monitoring shows that grafting polymer of PVA-g-PMMA was formed mainly at the stage-1 of the emulsion polymerization. TEM images show, the PVA-SH shell was fragmentary when adding SDS at initial stage and integrated when adding at particle growing or final stage. The particle size turns to be smaller when delayed adding SDS surfactant. Triethanolamine, a co-regulator of PVA-SH, controlled the M to 50 000-70 000 and reduced the PDI to 1.5-1.7. The acrylic dispersions with 0.8wt%-1.5wt% PVA-SH1 can be spray-dried into super dispersible polymer powder （SDPP）, which can easily disperse in water and form recon- stituted dispersions with an average particle size smaller than 1 micron.
文摘Electrospun nanofibers present a new and rapidly growing research area due to their pronounced micro and nano characteristics associated with high surface area to volume ratio. Poly(styrene-co-acrylamide) and polystyrene polymers were synthesized by boiling temperature soap free emulsion polymerization in aqueous medium with potassium peroxosulphate as the initiator. The resulting polymers were dissolved in dimethylformamide and teterahydrofuran (DMF: THF) (4:1) to form polymer solutions that were electrospun into fiber mats with diameters ranging from 1.84 - 2.53 μm and 5.01 μm, respectively. The fibers were characterized by Fourier transform infrared spectroscopy (FTIR) equipped with universal ATR sampling accessory (4000 - 400 cm-1). The morphology and size were examined by a scanning electron miscroscope (SEM) and the thermal properties by thermogravimetric analysis (TGA). The FTIR spectra of the poly(styrene-co-acrylamide) revealed the presence of acrylamide on the polystyrene chain. Thus, surface modification of polystyrene with acrylamide is possible in a single step polymerization reaction prior to electrospinning.
文摘Poly (acrylonitrile-co-vinyl acetate)/polypyrrole composite particles with uniform size and morphology have been synthesized using one-step polymerization that involves swelling and coating of polypyrrole (PPy) into P (AN-co-VAc) latex nanoparticles. As an initial stage, free radical copolymerization of acrylonitrile (AN) and vinyl acetate (VAc) was synthesized by emulsion polymerization using ammonium persulfate (APS) and dodecyl benzene sulfonic acid salt (DBSA) as a surfactant. P (AN-co-VAc)/PPy composites were obtained first time by in situ addition of the pyrrole into the reaction medium. The electrospun P (AN-co-VAc)/PPy nanofibers were obtained from the nanoparticles with better properties and the effect of PPy on the morphology of nanofibers was studied by scanning electron microscopy (SEM). High degree of homogeneity and molecular order induced by molecular dispersion of polypyrrole on copolymer matrix without phase separation improve the transport properties and stability of polypyrrole, which are critical for high-performance organic electronics.
基金National Nature Science Foundation of China grant number: 50803032, 10925208, 11032012, 11002016 and 30800217Fundamental Research Funds for the Central Universities
文摘This research investigates the formation of chitosan/poly （L-lactide） （CS/PLLA） porous composite scaffold using a novel emulsion freeze-drying technique. First, an oil in-water （O/W） emulsification system was used in the presence of surfactant Tween-80, in which CS solution was used as the water phase and PLLA solution was used as the oil phase. The emulsion was observed by inverted microscope （× 200）. The emulsion droplet was spherical and uniform in size. FT-IR analysis revealed that there were hydrogen bonding interactions between CS and PLLA components. The microstructure and physical properties of the scaffolds were also analyzed. The SEM results showed that composite scaffolds formed well interconnected pore structure and homogenous distribution of CS and PLLA. When the content of PLLA reached 50%, the porosity of CS/PLLA composite scaffolds were between 83 %-91% and density in the range of 0.047 to 0.11 g/era3. The porosity showed a slight decrease and the density increased with the increase of PLLA dose. The compressive strength increased from 0.32 to 0.43 MPa, while the compressive modulus increased from 1.99 to 3.91 MPa as the PLLA contents increased from 10% to 50%.
基金financially supported by the National Natural Science Foundation of China(No.21274084)
文摘A series of well-defined core cross-linked star （CCS） polymeric ionic liquids （PILs） were synthesized via a three- step approach. First, the styrenic imidazole-based CCS polymer （S-PVBnIm） was prepared by the RAFT-mediated heterogeneous polymerization in a water/ethanol solution, followed by the quaternization of S-PVBnIm with bromoalkanes and anion exchange. The CCS polymers were characterized by gel permeation chromatography （GPC）, nuclear magnetic resonance （NMR） spectroscopy, Fourier transform infrared spectroscopy （FTIR）, thermal gravimetric analysis （TGA）, and differential scanning calorimetry （DSC）. The obtained CCS polymers were used as the effective emulsifiers for oil-in-water high internal phase emulsions （HIPEs）. Multiple oils with different polarity including n-dodecane, undecanol, toluene and octanol were emulsified using 0.5 wt% S-PVBnIm aqueous solution under the acidic condition to form HIPEs with long-term stabilities. The excellent emulsification properties of CCS PILs were demonstrated by HIPE formation for a variety of oils. The properties of HIPEs in terms of emulsion type and oil droplet size were characterized by the confocal laser scanning microscopy （CLSM）. The intriguing capability of CCS PILs to stabilize HIPEs of various oils holds great potentials for the practical applications.
文摘Submicron-sized P（St-NaSS） latexes were prepared via a semi-continuous emulsion copolymerization of styrene （St） and sodium styrene sulphonate （NaSS） in the presence of anionic surfactant, in which NaSS aqueous solution and St were separately dropwise charged into the polymerization system at the same time. The hydrodynamic diameter of the latex particles was measured by dynamic light scattering （DSL） method, and the NaSS unit content of the purified copolymer by water extraction was calculated based on the elementary analysis. Results showed that the copolymerization could be performed smoothly with the monomer conversion more than 96% in the absence of crosslinker, and PNaSS homopolymer could be removed from the latex product by water extraction for 28 h. The weight loss in the water extraction tended to decrease and the NaSS unit content of the purified copolymer tended to increase with the increase of monomer feeding time, and both of them increased with the increase of NaSS/St mole ratio in the charge. The introduction of divinyl benzene （DVB） could decrease the weight loss in the water extraction and increase the NaSS unit content of the purified copolymer. When 25/75 mole ratio of NaSS/St and 11 mol% DVB of total NaSS and St were used in the recipe, and the monomer feeding time was 3 h in copolymerization, the NaSS unit content of the purified copolymer reached 7.31 mol%.
