Copolymer of acrylic acid and maleic acid(PMA)was used to remove Hg^2+from aqueous solution by complexation-ultrafiltration(C-UF)through rotating disk membrane(RDM).The effects of P/M(mass ratio of PMA to metal ions),...Copolymer of acrylic acid and maleic acid(PMA)was used to remove Hg^2+from aqueous solution by complexation-ultrafiltration(C-UF)through rotating disk membrane(RDM).The effects of P/M(mass ratio of PMA to metal ions),pH and rotation speed(N)on the interception of Hg^2+were investigated.The interception could reach 99.7%at pH 7.0,P/M 6 and N less than 1890 r/min.The shear stability of PMA-Hg complex was studied by RDM.The critical rotation speed,at which the interception starts to decrease,was 1890 r/min,and the critical shear rate,the smallest shear rate at which PMA-Hg complex begins to dissociate,was 2.50×10^5s^-1 at pH 7.0.Furthermore,the critical radii were obtained at different rotation speeds and pHs.The results showed that the critical radius decreased with the rotation speed and increased with pH.Shear induced dissociation coupling with ultra?ltration(SID-UF)was efficiently used to recover Hg^2+and PMA.展开更多
According to the equivalent circuit model(ECM),finite element model(FEM) and physical experiment,the LIDEP force induced by the spatial variations of the phase of AC electric fields produced by the bright and dark reg...According to the equivalent circuit model(ECM),finite element model(FEM) and physical experiment,the LIDEP force induced by the spatial variations of the phase of AC electric fields produced by the bright and dark regions on the photoconductive layer was demonstrated.Besides,the phenomenon of the light-induced electro-rotation(LIER) caused by the light-induced rotating electric field was confirmed numerically and experimentally for the first time.It may be helpful to go out of the dilemma that only the dipole moment model,based on the effect of light-induced partial potentials,can be used for LIDEP theoretical calculation currently.Through the FEM simulation and the electro-rotating experiment of yeast cells,it was found that the direction of yeast's LIER is relevant to the distance between its location and the edge of optical electrode,and the spin velocity of LIER is inversely proportional to that distance.Nevertheless,the LIER torques in the three-electrode mode show a non-uniform distribution where the LIDEP forces are harmful for a particle spinning stably around a fixed axis.Moreover,a four-electrode double-layer mode was proposed for the first time and the finite element simulation results agreed with the expected design,suggesting a new way for the dielectric spectrum measurement based on LIER.展开更多
Eight chiral vinylterphenyl monomers, （＋）-2,5-bis{4＇-[（S）-1＂-methylpropyloxy]phenyl}styrene （Ia）, （＋）-2,5-bis{4＇-[（S）-2＂- methylbutyloxy]phenyl}styrene （Ib）, （＋）-2,5-bis{4＇-[（S）-3＂-methylpenty...Eight chiral vinylterphenyl monomers, （＋）-2,5-bis{4＇-[（S）-1＂-methylpropyloxy]phenyl}styrene （Ia）, （＋）-2,5-bis{4＇-[（S）-2＂- methylbutyloxy]phenyl}styrene （Ib）, （＋）-2,5-bis{4＇-[（S）-3＂-methylpentyloxy]phenyl}styrene （Ic）, （＋）-2,5-bis{4＇-[（S）-4＂- methylhexyloxy]phenyl}styrene （Id）, （-）-2,5-bis{4＇-[（R）-1＂-methylpropyloxy]phenyl}styrene （le）, （＋）-2-/4＇-[（S）-l＂-methyl- propyloxy]phenyl}-5-{4＇-[（R）-1＂-methylpropyloxy]phenyl}styrene （Ⅱa）, （-）-2-{4＇-[（R）-1＂-methylpropyloxy]phenyl}-5-{4＇- [（S）- 1 ＂-methylpropyloxy]phenyl } styrene （lib）, and （＋）-2- { 4＇-[（S）-2＂-methylbutyloxy]phenyl }-5- { 4＇-[（S）- 1＂-methylpropyl- oxy]phenyl}styrene （Ⅲ）, were synthesized and radically polymerized. These molecules were designed to further understand long-range chirality transfer in radical polymerization and to possibly tune the chiroptical properties of the polymers by varying the spatial configuration, position, and various combination of the stereogenic centers at the ends ofp-terphenyl pendants. The resultant polymers adopted helical conformations with a predominant screw sense. When the stereogenic centers ran away from the terphenyl group as in Ⅰb-d, the corresponding polymers changed the direction of optical rotation in an alternative way and showed no obvious stereomutation upon annealing in tetrahydrofuran. The two stereogenic centers of Ⅱa, Ⅱb, and Ⅲ acted concertedly in chiral induction, whereas those of la and Ie played a counteractive role. The five polymers derived from Ⅰa, Ⅰe, Ⅱa, Ⅱb, and Ⅲ underwent stereomutation when annealed in tetrahydrofuran. The polymers PIa-e had good thermal stability and high glass transition temperatures （Tgs）. They generated liquid crystalline phases at above Tgs that could be kept upon cooling, with the exception of Pie. This result was consistent with the extended helical structures.展开更多
基金Project(21476265)supported by the National Natural Science Foundation of China。
文摘Copolymer of acrylic acid and maleic acid(PMA)was used to remove Hg^2+from aqueous solution by complexation-ultrafiltration(C-UF)through rotating disk membrane(RDM).The effects of P/M(mass ratio of PMA to metal ions),pH and rotation speed(N)on the interception of Hg^2+were investigated.The interception could reach 99.7%at pH 7.0,P/M 6 and N less than 1890 r/min.The shear stability of PMA-Hg complex was studied by RDM.The critical rotation speed,at which the interception starts to decrease,was 1890 r/min,and the critical shear rate,the smallest shear rate at which PMA-Hg complex begins to dissociate,was 2.50×10^5s^-1 at pH 7.0.Furthermore,the critical radii were obtained at different rotation speeds and pHs.The results showed that the critical radius decreased with the rotation speed and increased with pH.Shear induced dissociation coupling with ultra?ltration(SID-UF)was efficiently used to recover Hg^2+and PMA.
基金supported by the Major Program of the National Natural Science Foundation of China (Grant No. 91023024)the New Century Elitist Program by Ministry of Education of China (Grant No.NCET-07-0180)the Technology Supported Research Program from Jiangsu Province (Grant No. BE2009054)
文摘According to the equivalent circuit model(ECM),finite element model(FEM) and physical experiment,the LIDEP force induced by the spatial variations of the phase of AC electric fields produced by the bright and dark regions on the photoconductive layer was demonstrated.Besides,the phenomenon of the light-induced electro-rotation(LIER) caused by the light-induced rotating electric field was confirmed numerically and experimentally for the first time.It may be helpful to go out of the dilemma that only the dipole moment model,based on the effect of light-induced partial potentials,can be used for LIDEP theoretical calculation currently.Through the FEM simulation and the electro-rotating experiment of yeast cells,it was found that the direction of yeast's LIER is relevant to the distance between its location and the edge of optical electrode,and the spin velocity of LIER is inversely proportional to that distance.Nevertheless,the LIER torques in the three-electrode mode show a non-uniform distribution where the LIDEP forces are harmful for a particle spinning stably around a fixed axis.Moreover,a four-electrode double-layer mode was proposed for the first time and the finite element simulation results agreed with the expected design,suggesting a new way for the dielectric spectrum measurement based on LIER.
基金supported by the National Natural Science Foundation of China(21274003)the Research Fund for Doctoral Program of Higher Education of Ministry of Education(20110001110084)
文摘Eight chiral vinylterphenyl monomers, （＋）-2,5-bis{4＇-[（S）-1＂-methylpropyloxy]phenyl}styrene （Ia）, （＋）-2,5-bis{4＇-[（S）-2＂- methylbutyloxy]phenyl}styrene （Ib）, （＋）-2,5-bis{4＇-[（S）-3＂-methylpentyloxy]phenyl}styrene （Ic）, （＋）-2,5-bis{4＇-[（S）-4＂- methylhexyloxy]phenyl}styrene （Id）, （-）-2,5-bis{4＇-[（R）-1＂-methylpropyloxy]phenyl}styrene （le）, （＋）-2-/4＇-[（S）-l＂-methyl- propyloxy]phenyl}-5-{4＇-[（R）-1＂-methylpropyloxy]phenyl}styrene （Ⅱa）, （-）-2-{4＇-[（R）-1＂-methylpropyloxy]phenyl}-5-{4＇- [（S）- 1 ＂-methylpropyloxy]phenyl } styrene （lib）, and （＋）-2- { 4＇-[（S）-2＂-methylbutyloxy]phenyl }-5- { 4＇-[（S）- 1＂-methylpropyl- oxy]phenyl}styrene （Ⅲ）, were synthesized and radically polymerized. These molecules were designed to further understand long-range chirality transfer in radical polymerization and to possibly tune the chiroptical properties of the polymers by varying the spatial configuration, position, and various combination of the stereogenic centers at the ends ofp-terphenyl pendants. The resultant polymers adopted helical conformations with a predominant screw sense. When the stereogenic centers ran away from the terphenyl group as in Ⅰb-d, the corresponding polymers changed the direction of optical rotation in an alternative way and showed no obvious stereomutation upon annealing in tetrahydrofuran. The two stereogenic centers of Ⅱa, Ⅱb, and Ⅲ acted concertedly in chiral induction, whereas those of la and Ie played a counteractive role. The five polymers derived from Ⅰa, Ⅰe, Ⅱa, Ⅱb, and Ⅲ underwent stereomutation when annealed in tetrahydrofuran. The polymers PIa-e had good thermal stability and high glass transition temperatures （Tgs）. They generated liquid crystalline phases at above Tgs that could be kept upon cooling, with the exception of Pie. This result was consistent with the extended helical structures.
