Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interfac...Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interface anchoring,and inorganic particles have gained extensive attention recently owing to their large interfacial desorption energy,while their low affinity to bulk components is a drawback.In this study,an interfacial atom transfer radical polymerization(ATRP)technique was employed to grow polystyrene(PS)and poly(2-hydroxyethyl methacrylate)(PHEMA)simultaneously on different hemispheres of Br-functionalized SiO_(2) nanoparticles to stabilize a Pickering emulsion,whereby a brush-type Janus nanoparticle(SiO_(2)@JNP)was developed.The polymer brushes were well-characterized,and the Janus feature was validated by transmission electron microscope(TEM)observation of the sole hemisphere grafting of SiO_(2)-PS as a control sample.SiO_(2)@JNP was demonstrated to be an efficient compatibilizer for a PS/poly(methyl methacrylate)(PMMA)immiscible blend,and the droplet-matrix morphology was significantly refined.The mechanical strength and toughness of the blend were synchronously enhanced at a low content SiO_(2)@JNP optimized~0.9 wt%,with the tensile strength,elongation at break and impact strength increased by 17.7%,26.6%and 19.6%,respectively.This enhancement may be attributed to the entanglements between the grafted polymer brushes and individual components that improve the particle-bulk phase affinity and enforce interfacial adhesion.展开更多
Polystyrene coated silica（SiO_2@PS） core-shell composite particles with averaged diameter of about 290 nm were prepared by in situ emulsion polymerization of styrene on the surface ofγ-methacryloxypropyltrimethoxys...Polystyrene coated silica（SiO_2@PS） core-shell composite particles with averaged diameter of about 290 nm were prepared by in situ emulsion polymerization of styrene on the surface ofγ-methacryloxypropyltrimethoxysilane grafted SiO_2 nanoparticles of 20-50 nm in diameter.Rheological behavior and dispersion stability of SiO_2@PS suspension in 10 wt%PS solution were compared with suspensions of untreated SiO_2 and silane modified SiO_2 nanoparticles.Suspensions of the untreated and the silane modified SiO_2 exhibited obvious shear thinning.The SiO-2@PS suspension exhibits shear viscosity considerably smaller than suspensions of untreated and silane modified SiO_2 at low shear rates.Transmission electron microscopy showed that the composite particles can uniformly and stably disperse in PS solution compared to other suspensions,implying that the PS shell can effectively enhance the particle compatibility with PS macromolecules in solution.展开更多
The monomolecular particle agglomerates of polystyrenes were obtained by freeze-drying of its very dilute solutions of 1.3 x 10(-5)-2.0 x 10(-5) g/mL in benzene:cylcohexane (100:1) solvents, and they were annealed at ...The monomolecular particle agglomerates of polystyrenes were obtained by freeze-drying of its very dilute solutions of 1.3 x 10(-5)-2.0 x 10(-5) g/mL in benzene:cylcohexane (100:1) solvents, and they were annealed at room temperature for hundred days before use. According to C-13-NMR measurement the polystyrenes should be practically atactic. The number average molecular weights of the samples are 2.80 x 10(3), 2.00 x 10(4), and 1.55 x 10(6), respectively. The freeze-dried aPS with a molecular weight higher than 10(4) show two new IR absorption bands at 1098 and 1261 cm(-1), which are absent in the normal aPS and freeze-dried styrene oligomer. It was also found that the low molecular weight samples can only form powders, whereas the freeze-dried aPS with higher molecular weight form a mixture of powders and fibrils, of which the longer fibrils show a much stronger 1261 cm(-1) band than the shorter fibrils and the powder. It seems that the 1261 cm(-1) band corresponds to the stacking behavior of monomolecular particles.展开更多
Uniform polystyrene hollow particles were prepared successfully by employing SPG (Shirasu porous glass) emulsification technique. The oil phase composed of monomer [styrene (St) and N,N’-dimethylamino ethylmethacryla...Uniform polystyrene hollow particles were prepared successfully by employing SPG (Shirasu porous glass) emulsification technique. The oil phase composed of monomer [styrene (St) and N,N’-dimethylamino ethylmethacrylate (DMAEMA)], hexadecane (HD) and initiator was permeated through the uniform pores of SPG membrane into the aqueous phase (containing stabilizer, emulsifier and water-soluble inhibitor ) by a gas pressure to form uniform droplets. The droplets were then polymerized at 70℃. It was found that the hollow particles were obtained by adding a small amount of DMAEMA into the oil phase and by using NaNo2 as the water-soluble inhibitor, while only one-hole particles were obtained without adding DMAEMA, or when using diaminophenylene (DAP) or hydroquinone (HQ) as the inhibitor. The formation mechanism was discussed by the view of interfacial tensions between polymer and aqueous phase, HD and aqueous phase, and HD and polymer. Further more, it was found that hollow particles can be obtained even when DMAEMA content in the oil phase was very low, by increasing HD to high value.展开更多
The film formation process of micro-PS particles (diameter 742 nm) and nano-PS particles (diameter 29 nm) was studied by atomic force microscopy and differential scanning calorimetry. During a step heating process, th...The film formation process of micro-PS particles (diameter 742 nm) and nano-PS particles (diameter 29 nm) was studied by atomic force microscopy and differential scanning calorimetry. During a step heating process, the particles were annealed for 0.5 h at each selected temperature. It was found that the deformation and interdiffusion temperatures of the micro-PS particles are ca. 120-130degreesC and 140-150degreesC, that of the nano-PS particles are 90degreesC and 100-110degreesC respectively. The DSC traces of nano-PS particles showed that there was an exothermic peak near T-g after annealing for 0.5 h at the selected temperatures below 90degreesC; otherwise, the exothermic peak disappeared after annealing at 100degreesC or above. Compared with the micro-PS particles, the sintering process of nano-PS particles occurs at much lower temperature determined by the confined state of polymer chains with higher conformational energy in nano-particles, and completes in a much narrower temperature range driven mainly by the larger total surface energy.展开更多
C spin-lattice relaxtion times for polystyrene nanolatex particles have been investigated. It was found that the dramatic increase at 80℃ annealing temperature is well below the Tg temperature of bulk polystyrene, t...C spin-lattice relaxtion times for polystyrene nanolatex particles have been investigated. It was found that the dramatic increase at 80℃ annealing temperature is well below the Tg temperature of bulk polystyrene, the increase of relaxation time of aromatic carbons is larger than that of for aliphatic carbons at transition annealing temperature.展开更多
A highly crosslinked, monodispersed polystyrene（PS） particle was prepared by a seeded batch dispersion polymerization with a monomer absorption method. Prior to polymerization, 1,9 lam monodispersed PS seed particle...A highly crosslinked, monodispersed polystyrene（PS） particle was prepared by a seeded batch dispersion polymerization with a monomer absorption method. Prior to polymerization, 1,9 lam monodispersed PS seed particles were treated under an optimum condition of monomer absorption. The effects of divinylbenzebe（DVB） concentration and polymerization temperature were examined for styrene（in PS seed）/styrene（in the second stage） mass ratio of 1：1 in the medium range of EtOH/water mass ratio of 100/0-80/20 and 2.3 μm uniform crosslinked PS particles containing 15%-20% （mass fraction） DVB were prepared at 60-70 ℃. The results show that monomer absorption before the second stage of polymerization is more effective to prepare highly crosslinked monodispersed PS particles.展开更多
This study tackles current environmental challenges by developing innovative and eco-friendly particle boards utilizing sorghum husk, combined with recycled expanded polystyrene (EPS). This dual eco-responsible approa...This study tackles current environmental challenges by developing innovative and eco-friendly particle boards utilizing sorghum husk, combined with recycled expanded polystyrene (EPS). This dual eco-responsible approach valorizes sorghum husk, often deemed agricultural waste, and repurposes EPS, a plastic waste, thus contributing to CO2 emission reduction and effective waste management. The manufacturing process involves dissolving recycled polystyrene within a solvent to create a binder, which is then mixed with sorghum husk and cold-pressed into composite boards. The study explores the impact of two particle sizes (fine and coarse) and two different concentrations of the recycled EPS binder. Results demonstrate significant variations in the boards’ mechanical properties, displaying a range of Modulus of Rupture (MOR) from 0.84 MPa to 3.85 MPa, and Modulus of Elasticity (MOE) spanning from 658.13 MPa to 1313.25 MPa, influenced by the binder concentration and particle size. These characteristics suggest that the boards can be effectively used in various construction applications, including interior decoration, false ceilings, and potentially for furniture and door manufacturing when combined with appropriate coatings. This study not only exemplifies the valorization of plastic and agricultural wastes but also offers a practical, localized solution to global climate change challenges by promoting sustainable construction materials.展开更多
Monodisperse crosslinked polystyrene （CPS） particles were prepared through the normal emulsion polymerization method by adding crosslinker--divinylbenzene （DVB） into the reaction system after polystyrene （PS） pa...Monodisperse crosslinked polystyrene （CPS） particles were prepared through the normal emulsion polymerization method by adding crosslinker--divinylbenzene （DVB） into the reaction system after polystyrene （PS） particles grew to -80% of the final size. When the amount of crosslinker DVB added was less than 6.17 wt% based on styrene, the prepared CPS particles were spherical and uniform and the size of the CPS particles could be predicted through the normal emulsion method. The glass transition temperature （Tg） of the prepared CPS particles was higher than that of un-crosslinked PS particles and, the more crosslinker that was added, the higher the Tg of CPS Particles. The prepared CPS particles had strong resistance to organic solvents.展开更多
Monooctadecyl maleate, as a polymerizable surfactant, was synthesized by the mono-esterification of maleic anhydride and octadecanol, and was utilized to surface-modify nano-Fe3O4 particles. A polymerizable magnetic f...Monooctadecyl maleate, as a polymerizable surfactant, was synthesized by the mono-esterification of maleic anhydride and octadecanol, and was utilized to surface-modify nano-Fe3O4 particles. A polymerizable magnetic fluid was obtained by directly dispersing modified nano-Fe3O4 particles into styrene monomer, and the polystyrene/nano-Fe3O4 composite was prepared through free radical polymerization of polymerizable magnetic fluid. The structure and dispersion status in different dispersion phases of modified nano-Fe3O4 particles were studied by Fourier transform infrared （FTIR） spectrometry, X-ray diffraction （XRD） and transmission electron microscopy （TEM）, respectively. The experimental results show that the nano-Fe3O4 particles modified by monooctadecyl maleate with the size of about 7-10 nm can be uniformly dispersed into styrene and fixed in the composite during the procedure of polymerization. Thermogravimetric analysis （TGA） and vibrating sample magnetometry （VSM） indicate that the thermal stability of polystyrene/nano-Fe3O4 composite is improved compared to that of pure polystyrene, and the composite is a sort of superparamagnetic materials.展开更多
Fe_3O_4/Polystyrene(PSt) magnetic particles with core/shell structure have been prepared in thepresence of Fe_3O_4 magnetic fluid in ethanol/water medium by dispersion polymeriation of styrene. A Fe_3O_4particle forma...Fe_3O_4/Polystyrene(PSt) magnetic particles with core/shell structure have been prepared in thepresence of Fe_3O_4 magnetic fluid in ethanol/water medium by dispersion polymeriation of styrene. A Fe_3O_4particle formation mechanism was proposed. According to this mechanism, the size of particle nuclei isdetermined by the extent of aggregation of Fe_3O_4 /oligomer. Magnetic particles with diameter ranging from 5to 200 μm were prepared under different reaction conditions. Some polymerization parameters such as theconcentration of monomer, stabilizer, initiator, and ethanol which affect particle size and size distribution arediscussed and their effect on particle formation are explained by the proposed mechanism.展开更多
A new method was developed for the determination of the size distribution of nano-particles by capillary zone electrophoresis (CZE). Scattering effect of nanoparticles was studied . This method for the determination...A new method was developed for the determination of the size distribution of nano-particles by capillary zone electrophoresis (CZE). Scattering effect of nanoparticles was studied . This method for the determination of size distribution was statistical.展开更多
The novel method for preparing the polymer composite particles has been developed. It was tried to prepare polymer composite particles composed of polystyrene and carbon black with the phase separation method followed...The novel method for preparing the polymer composite particles has been developed. It was tried to prepare polymer composite particles composed of polystyrene and carbon black with the phase separation method followed by suspension polymerization. In order to prepare the polymer composite particles with the more uniform diameter, the styrene monomer droplets containing carbon black were formed with phase separation emulsification in which ethyl alcohol and water were used as the good solvent and the poor solvent for styrene monomer, respectively. In the experiment, the surfactant species and their concentrations, the pouring velocity of water and the weight ratio of carbon black to styrene monomer were mainly changed. Water was poured at the given pouring velocity into ethyl alcohol in which styrene monomer and an initiator were dissolved and carbon black was dispersed beforehand. The spherical polymer composite particles containing carbon black were prepared with Tween 20 and Tween 80 of nonionic surfactants and the irregular polymer composite particles were prepared with PVA, SDS and Kotamine. The diameters of polymer composite particles increased with the pouring velocity of water and with the weight ratio of carbon black to styrene monomer.展开更多
文摘Fluoroalkyl end-capped vinyltrimethoxysilane-<i><span style="font-family:Verdana;">N</span></i><span><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;">N</span></i></span><span style="font-family:Verdana;">-dimethylacrylamide cooli</span><span style="font-family:;" "=""><span style="font-family:Verdana;">gomer [R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(CH</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">-CHSi(OMe)</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">x</span></sub></i><span style="font-family:Verdana;">-(CH</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">-CHC(=O)NMe</span><sub><span style="font-family:Verdana;">2</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">y</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">;R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;"> = CF(CF</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;">)OC</span><sub><span style="font-family:Verdana;">3</span></sub><span style="font-family:Verdana;">F</span><sub><span style="font-family:Verdana;">7</span></sub><span style="font-family:Verdana;">:</span></span><span style="font-family:;" "=""><span style="font-family:Verdana;"> R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM)</span><i><sub><span style="font-family:Verdana;">x</span></sub></i><span style="font-family:Verdana;">-(DMAA)</span><i><sub><span style="font-family:Verdana;">y</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">] was synthesized by reaction of fluoroalkanoyl peroxide [R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-C(=O)O-O(O=)C-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">] with vinyltrimethoxysilane (VM) and </span><i><span style="font-family:Verdana;">N</span></i><span><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;">N</span></i></span><span style="font-family:Verdana;">-</span></span><span style="font-family:Verdana;">dimethylacrylamide (DMAA). The modified glass surface treated with the</span><span style="font-family:;" "=""><span style="font-family:Verdana;"> cooligomeric nanoparticles [R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM-SiO</span><sub><span style="font-family:Verdana;">3/2</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">x</span></sub></i><span style="font-family:Verdana;">-(DMAA)</span><i><sub><span style="font-family:Verdana;">y</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">] prepared under the sol-gel reaction of the cooligomer under alkaline conditions was found to exhibit an oleophobic/superhydrophilic property, although the corresponding fluorinated homooligomeric nanoparticles [R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM-SiO</span><sub><span style="font-family:Verdana;">3/2</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">n</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">] afforded an </span><span style="font-family:Verdana;">oleophobic/hydrophobic property on the modified surface under similar </span><span style="font-family:Verdana;">con</span><span><span style="font-family:Verdana;">ditions. R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM-SiO</span><sub><span style="font-family:Verdana;">3/2</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">n</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">/R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM-SiO</span><sub><span style="font-family:Verdana;">3/2</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">x</span></sub></i><span style="font-family:Verdana;">-(DMAA)</span><i><sub><span style="font-family:Verdana;">y</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">/</span><b><i><span style="font-family:Verdana;">PSt</span></i></b><span style="font-family:Verdana;"> (micro-sized</span></span> <span style="font-family:Verdana;">polystyrene particles) composites, which were prepared by the sol-gel reac</span><span style="font-family:Verdana;">tions of the corresponding homooligomer and cooligomer in the presence of </span><b><i><span style="font-family:Verdana;">PSt </span></i></b><span style="font-family:Verdana;">particle under alkaline conditions, provided an oleophobic/superhydrophilic </span><span style="font-family:Verdana;">property on the modified surface. However, it was demonstrated that the</span><span><span style="font-family:Verdana;"> surface wettability on the modified surface treated with the R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM-</span></span><span><span style="font-family:Verdana;">SiO</span><sub><span style="font-family:Verdana;">3/2</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">n</span></sub></i><span style="font-family:Verdana;">-</span></span></span><span style="font-family:;" "=""><span style="font-family:Verdana;">R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">/R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM-SiO</span><sub><span style="font-family:Verdana;">3/2</span></sub><span style="font-family:Verdana;">)</span><i><sub><span style="font-family:Verdana;">x</span></sub></i><span style="font-family:Verdana;">-(DMAA)</span><i><sub><span style="font-family:Verdana;">y</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">/</span><b><i><span style="font-family:Verdana;">PSt</span></i></b><span style="font-family:Verdana;"> composites changes dramatically from oleophobic/superhydrophilic to superoleophilic/superhydrophilic </span><span style="font-family:Verdana;">and superoleophilic/superhydrophobic characteristics, increasing with </span><span style="font-family:Verdana;">greater </span><span><span style="font-family:Verdana;">feed ratios (mg/mg) of the R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;">-(VM)</span><i><sub><span style="font-family:Verdana;">n</span></sub></i><span style="font-family:Verdana;">-R</span><sub><span style="font-family:Verdana;">F</span></sub><span style="font-family:Verdana;"> homooligomer in homooligo</span></span><span style="font-family:Verdana;">mer/cooligo</span></span><span style="font-family:Verdana;">mer from 0 to 100 in the preparation of the composites. Such controlled surfac</span>
基金financially supported by the National Natural Science Foundation of China(Nos.22172028,21903015,and 22403017)Natural Science Foundation of Fujian Province of China(No.2022J05041)。
文摘Compatibilization is crucial for the blending of immiscible polymers to develop high-performance composites;however,traditional compatibilization by copolymers(pre-made or in-situ generation)suffers from weak interface anchoring,and inorganic particles have gained extensive attention recently owing to their large interfacial desorption energy,while their low affinity to bulk components is a drawback.In this study,an interfacial atom transfer radical polymerization(ATRP)technique was employed to grow polystyrene(PS)and poly(2-hydroxyethyl methacrylate)(PHEMA)simultaneously on different hemispheres of Br-functionalized SiO_(2) nanoparticles to stabilize a Pickering emulsion,whereby a brush-type Janus nanoparticle(SiO_(2)@JNP)was developed.The polymer brushes were well-characterized,and the Janus feature was validated by transmission electron microscope(TEM)observation of the sole hemisphere grafting of SiO_(2)-PS as a control sample.SiO_(2)@JNP was demonstrated to be an efficient compatibilizer for a PS/poly(methyl methacrylate)(PMMA)immiscible blend,and the droplet-matrix morphology was significantly refined.The mechanical strength and toughness of the blend were synchronously enhanced at a low content SiO_(2)@JNP optimized~0.9 wt%,with the tensile strength,elongation at break and impact strength increased by 17.7%,26.6%and 19.6%,respectively.This enhancement may be attributed to the entanglements between the grafted polymer brushes and individual components that improve the particle-bulk phase affinity and enforce interfacial adhesion.
基金supported by the National Natural Science Foundation of China(No.51073136)the Fundamental Research Funds for the Central Universities of China(No.2010QNA4011)
文摘Polystyrene coated silica（SiO_2@PS） core-shell composite particles with averaged diameter of about 290 nm were prepared by in situ emulsion polymerization of styrene on the surface ofγ-methacryloxypropyltrimethoxysilane grafted SiO_2 nanoparticles of 20-50 nm in diameter.Rheological behavior and dispersion stability of SiO_2@PS suspension in 10 wt%PS solution were compared with suspensions of untreated SiO_2 and silane modified SiO_2 nanoparticles.Suspensions of the untreated and the silane modified SiO_2 exhibited obvious shear thinning.The SiO-2@PS suspension exhibits shear viscosity considerably smaller than suspensions of untreated and silane modified SiO_2 at low shear rates.Transmission electron microscopy showed that the composite particles can uniformly and stably disperse in PS solution compared to other suspensions,implying that the PS shell can effectively enhance the particle compatibility with PS macromolecules in solution.
文摘The monomolecular particle agglomerates of polystyrenes were obtained by freeze-drying of its very dilute solutions of 1.3 x 10(-5)-2.0 x 10(-5) g/mL in benzene:cylcohexane (100:1) solvents, and they were annealed at room temperature for hundred days before use. According to C-13-NMR measurement the polystyrenes should be practically atactic. The number average molecular weights of the samples are 2.80 x 10(3), 2.00 x 10(4), and 1.55 x 10(6), respectively. The freeze-dried aPS with a molecular weight higher than 10(4) show two new IR absorption bands at 1098 and 1261 cm(-1), which are absent in the normal aPS and freeze-dried styrene oligomer. It was also found that the low molecular weight samples can only form powders, whereas the freeze-dried aPS with higher molecular weight form a mixture of powders and fibrils, of which the longer fibrils show a much stronger 1261 cm(-1) band than the shorter fibrils and the powder. It seems that the 1261 cm(-1) band corresponds to the stacking behavior of monomolecular particles.
文摘Uniform polystyrene hollow particles were prepared successfully by employing SPG (Shirasu porous glass) emulsification technique. The oil phase composed of monomer [styrene (St) and N,N’-dimethylamino ethylmethacrylate (DMAEMA)], hexadecane (HD) and initiator was permeated through the uniform pores of SPG membrane into the aqueous phase (containing stabilizer, emulsifier and water-soluble inhibitor ) by a gas pressure to form uniform droplets. The droplets were then polymerized at 70℃. It was found that the hollow particles were obtained by adding a small amount of DMAEMA into the oil phase and by using NaNo2 as the water-soluble inhibitor, while only one-hole particles were obtained without adding DMAEMA, or when using diaminophenylene (DAP) or hydroquinone (HQ) as the inhibitor. The formation mechanism was discussed by the view of interfacial tensions between polymer and aqueous phase, HD and aqueous phase, and HD and polymer. Further more, it was found that hollow particles can be obtained even when DMAEMA content in the oil phase was very low, by increasing HD to high value.
基金This work was funded by the Special Funds for Major State Basic Research Project (Grant No. 95-12-G1999064800) and National Natural Science Foundation of China (Grant No. 20004011 & 20023003).
文摘The film formation process of micro-PS particles (diameter 742 nm) and nano-PS particles (diameter 29 nm) was studied by atomic force microscopy and differential scanning calorimetry. During a step heating process, the particles were annealed for 0.5 h at each selected temperature. It was found that the deformation and interdiffusion temperatures of the micro-PS particles are ca. 120-130degreesC and 140-150degreesC, that of the nano-PS particles are 90degreesC and 100-110degreesC respectively. The DSC traces of nano-PS particles showed that there was an exothermic peak near T-g after annealing for 0.5 h at the selected temperatures below 90degreesC; otherwise, the exothermic peak disappeared after annealing at 100degreesC or above. Compared with the micro-PS particles, the sintering process of nano-PS particles occurs at much lower temperature determined by the confined state of polymer chains with higher conformational energy in nano-particles, and completes in a much narrower temperature range driven mainly by the larger total surface energy.
基金This work was supported by National Key Project for Fundamental Research (N.95-11) and National Natural Science Foundation of Ch
文摘C spin-lattice relaxtion times for polystyrene nanolatex particles have been investigated. It was found that the dramatic increase at 80℃ annealing temperature is well below the Tg temperature of bulk polystyrene, the increase of relaxation time of aromatic carbons is larger than that of for aliphatic carbons at transition annealing temperature.
基金the second stage of BK21 program for supporting a fellowship
文摘A highly crosslinked, monodispersed polystyrene（PS） particle was prepared by a seeded batch dispersion polymerization with a monomer absorption method. Prior to polymerization, 1,9 lam monodispersed PS seed particles were treated under an optimum condition of monomer absorption. The effects of divinylbenzebe（DVB） concentration and polymerization temperature were examined for styrene（in PS seed）/styrene（in the second stage） mass ratio of 1：1 in the medium range of EtOH/water mass ratio of 100/0-80/20 and 2.3 μm uniform crosslinked PS particles containing 15%-20% （mass fraction） DVB were prepared at 60-70 ℃. The results show that monomer absorption before the second stage of polymerization is more effective to prepare highly crosslinked monodispersed PS particles.
文摘This study tackles current environmental challenges by developing innovative and eco-friendly particle boards utilizing sorghum husk, combined with recycled expanded polystyrene (EPS). This dual eco-responsible approach valorizes sorghum husk, often deemed agricultural waste, and repurposes EPS, a plastic waste, thus contributing to CO2 emission reduction and effective waste management. The manufacturing process involves dissolving recycled polystyrene within a solvent to create a binder, which is then mixed with sorghum husk and cold-pressed into composite boards. The study explores the impact of two particle sizes (fine and coarse) and two different concentrations of the recycled EPS binder. Results demonstrate significant variations in the boards’ mechanical properties, displaying a range of Modulus of Rupture (MOR) from 0.84 MPa to 3.85 MPa, and Modulus of Elasticity (MOE) spanning from 658.13 MPa to 1313.25 MPa, influenced by the binder concentration and particle size. These characteristics suggest that the boards can be effectively used in various construction applications, including interior decoration, false ceilings, and potentially for furniture and door manufacturing when combined with appropriate coatings. This study not only exemplifies the valorization of plastic and agricultural wastes but also offers a practical, localized solution to global climate change challenges by promoting sustainable construction materials.
基金National Basic Research Program of China(Grant No:2006CB932601)the Scientific Research Foundation for Returned Overseas Chinese Scholar,Ministry of Education
文摘Monodisperse crosslinked polystyrene （CPS） particles were prepared through the normal emulsion polymerization method by adding crosslinker--divinylbenzene （DVB） into the reaction system after polystyrene （PS） particles grew to -80% of the final size. When the amount of crosslinker DVB added was less than 6.17 wt% based on styrene, the prepared CPS particles were spherical and uniform and the size of the CPS particles could be predicted through the normal emulsion method. The glass transition temperature （Tg） of the prepared CPS particles was higher than that of un-crosslinked PS particles and, the more crosslinker that was added, the higher the Tg of CPS Particles. The prepared CPS particles had strong resistance to organic solvents.
基金Funded by the Natural Science Foundation of Guangdong Province (No. 020891)
文摘Monooctadecyl maleate, as a polymerizable surfactant, was synthesized by the mono-esterification of maleic anhydride and octadecanol, and was utilized to surface-modify nano-Fe3O4 particles. A polymerizable magnetic fluid was obtained by directly dispersing modified nano-Fe3O4 particles into styrene monomer, and the polystyrene/nano-Fe3O4 composite was prepared through free radical polymerization of polymerizable magnetic fluid. The structure and dispersion status in different dispersion phases of modified nano-Fe3O4 particles were studied by Fourier transform infrared （FTIR） spectrometry, X-ray diffraction （XRD） and transmission electron microscopy （TEM）, respectively. The experimental results show that the nano-Fe3O4 particles modified by monooctadecyl maleate with the size of about 7-10 nm can be uniformly dispersed into styrene and fixed in the composite during the procedure of polymerization. Thermogravimetric analysis （TGA） and vibrating sample magnetometry （VSM） indicate that the thermal stability of polystyrene/nano-Fe3O4 composite is improved compared to that of pure polystyrene, and the composite is a sort of superparamagnetic materials.
基金Project 59573011 was supported by National Natural Science Foundation of China
文摘Fe_3O_4/Polystyrene(PSt) magnetic particles with core/shell structure have been prepared in thepresence of Fe_3O_4 magnetic fluid in ethanol/water medium by dispersion polymeriation of styrene. A Fe_3O_4particle formation mechanism was proposed. According to this mechanism, the size of particle nuclei isdetermined by the extent of aggregation of Fe_3O_4 /oligomer. Magnetic particles with diameter ranging from 5to 200 μm were prepared under different reaction conditions. Some polymerization parameters such as theconcentration of monomer, stabilizer, initiator, and ethanol which affect particle size and size distribution arediscussed and their effect on particle formation are explained by the proposed mechanism.
文摘A new method was developed for the determination of the size distribution of nano-particles by capillary zone electrophoresis (CZE). Scattering effect of nanoparticles was studied . This method for the determination of size distribution was statistical.
文摘The novel method for preparing the polymer composite particles has been developed. It was tried to prepare polymer composite particles composed of polystyrene and carbon black with the phase separation method followed by suspension polymerization. In order to prepare the polymer composite particles with the more uniform diameter, the styrene monomer droplets containing carbon black were formed with phase separation emulsification in which ethyl alcohol and water were used as the good solvent and the poor solvent for styrene monomer, respectively. In the experiment, the surfactant species and their concentrations, the pouring velocity of water and the weight ratio of carbon black to styrene monomer were mainly changed. Water was poured at the given pouring velocity into ethyl alcohol in which styrene monomer and an initiator were dissolved and carbon black was dispersed beforehand. The spherical polymer composite particles containing carbon black were prepared with Tween 20 and Tween 80 of nonionic surfactants and the irregular polymer composite particles were prepared with PVA, SDS and Kotamine. The diameters of polymer composite particles increased with the pouring velocity of water and with the weight ratio of carbon black to styrene monomer.
