The chain reaction of 1,2-dichloroethane was initiated by photosensitization of SF_6 under the selective excitation using a cw CO_2 laser.Vinyl chloride with high purity was produced in the reaction process.The initia...The chain reaction of 1,2-dichloroethane was initiated by photosensitization of SF_6 under the selective excitation using a cw CO_2 laser.Vinyl chloride with high purity was produced in the reaction process.The initiation of the photosensitized chain reaction depends on the irradiated laser frequency.The mechanism of intermolecular resonant transfer of vibrational energy has been discussed.展开更多
A method for quantitative evaluating the enhancement of the rate of Type Ⅱ photosensitized oxidation by D_2O was suggested. The effect of substrate concentration on this process was also discussed.
The structures of 26 different congeners of polychlorinated biphenyls（PCBs, including monothrough deca-chlorinated） were optimized using density functional theory（DFT） calculations with the 6-31＋G（d,p） basis se...The structures of 26 different congeners of polychlorinated biphenyls（PCBs, including monothrough deca-chlorinated） were optimized using density functional theory（DFT） calculations with the 6-31＋G（d,p） basis set. The activation energies for the dechlorination of these systems were calculated for direct photodegradation and photosensitized degradation reaction pathways in the presence of natural organic matter（NOM）. The dechlorination mechanism of these PCBs and the ring-opening reaction mechanisms（using QST3 method） of the photosensitive degradation products were analyzed. The results showed that（i） the activation energy for the photosensitized degradation of PCBs was much lower than that of direct photodegradation;（ii） the degradation activities（i.e., C–Cl bond cleavage energies） were the same for both degradation pathways and followed the order ortho 〉 meta 〉 para;（iii） the degradation activities of asymmetric PCBs were higher than those of the corresponding symmetrical PCBs for the direct photodegradation and it was completely opposite in the photosensitive degradation;（iv） there was no correlation between the dissociation energy and the number of C–Cl bonds for the direct photodegradation and dechlorination products were all biphenyl;（v） the degradation activity of PCBs decreased as the number of C–Cl bonds increased in the presence of NOM; and（vi） even when the dechlorination reaction was incomplete, it produced chlorophenol. Furthermore, the free radicals of NOM led to the ring-opening reactions of PCBs via an initial addition step. The main site of these ring-opening reactions was the ortho position. Notably, the likelihood of ring-opening reactions occurring involving the degradation products increased as the degradation degree of PCBs increased.展开更多
The cerium ion(Ce4+) doped titania sol and nanocrystallites were prepared by chemical coprecipitation-peptization and hydrothermal synthesis methods, respectively. The X-ray diffraction pattern shows that Ce4+-TiO2 xe...The cerium ion(Ce4+) doped titania sol and nanocrystallites were prepared by chemical coprecipitation-peptization and hydrothermal synthesis methods, respectively. The X-ray diffraction pattern shows that Ce4+-TiO2 xerogel powder has semicrystalline structure and thermal sintering sample has crystalline structure. Ce4+-TiO2 nanocrystallites are composed of the major anatase phase titania (88.82 wt pct) and a small amount of crystalline cerium titanate. AFM micrograph shows that primary particle size of well-dispersed ultrafine sol particles is below 15 nm in diameter. The particle sizes are 30 nm for xerogel sample and 70 nm for nanocrystallites sample, which is different from the estimated values (2.41 nm and 4.53 nm) by XRD Scherrer's formula. The difference is mainly due to aggregation of nanocrystallites. The experimental results exhibit that photocatalysts of Ce4+-TiO2 sol and nanocrystallites have the ability to photodegrade reactive brilliant red dye (X-3B ) under visible light irradiation with the ion-TiO2/VIS/dye system. Moreover, Ce4+ doped titania sol has shown higher efficiency than the nanocrystallites sample in respect of potocatalytic activity. Meanwhile, dye photodegradation mechanisms are proposed to different photocatalytic reaction systems, which are dye photosensitization, ion-dye photosensitization and interband photocatalysis & dye photosensitization with respect to TiO2 nanocrystallites, Ce4+-TiO2 sol and Ce4+-TiO2 nanocrystallites system.展开更多
By introducing periodic switching signal associated with illumination to the Originator,a switched mathematical model has been established.The bifurcation sets are derived based on the characteristics of the equilibri...By introducing periodic switching signal associated with illumination to the Originator,a switched mathematical model has been established.The bifurcation sets are derived based on the characteristics of the equilibrium points.Two types of periodic oscillation,such as 2T-focus/cycle periodic switching and 2T-focus/focus periodic switching,have been observed,the mechanism of which is presented through the switching relationship.The distribution of eigenvalues related to the equilibrium points determined by two subsystems is discussed to interpret oscillation-increasing and oscillation-decreasing cascades of the periodic oscillations.Furthermore,the invariant subspaces of the equilibrium point are investigated to reveal the mechanism of dynamical phenomena in the periodic switching.展开更多
文摘The chain reaction of 1,2-dichloroethane was initiated by photosensitization of SF_6 under the selective excitation using a cw CO_2 laser.Vinyl chloride with high purity was produced in the reaction process.The initiation of the photosensitized chain reaction depends on the irradiated laser frequency.The mechanism of intermolecular resonant transfer of vibrational energy has been discussed.
文摘A method for quantitative evaluating the enhancement of the rate of Type Ⅱ photosensitized oxidation by D_2O was suggested. The effect of substrate concentration on this process was also discussed.
基金supported by the Fundamental Research Funds for the Central Universities in 2013(JB2013146)the Key Projects in the National Science&Technology Pillar Program in the Eleventh Five-Year Plan Period(2008BAC43B01)
文摘The structures of 26 different congeners of polychlorinated biphenyls（PCBs, including monothrough deca-chlorinated） were optimized using density functional theory（DFT） calculations with the 6-31＋G（d,p） basis set. The activation energies for the dechlorination of these systems were calculated for direct photodegradation and photosensitized degradation reaction pathways in the presence of natural organic matter（NOM）. The dechlorination mechanism of these PCBs and the ring-opening reaction mechanisms（using QST3 method） of the photosensitive degradation products were analyzed. The results showed that（i） the activation energy for the photosensitized degradation of PCBs was much lower than that of direct photodegradation;（ii） the degradation activities（i.e., C–Cl bond cleavage energies） were the same for both degradation pathways and followed the order ortho 〉 meta 〉 para;（iii） the degradation activities of asymmetric PCBs were higher than those of the corresponding symmetrical PCBs for the direct photodegradation and it was completely opposite in the photosensitive degradation;（iv） there was no correlation between the dissociation energy and the number of C–Cl bonds for the direct photodegradation and dechlorination products were all biphenyl;（v） the degradation activity of PCBs decreased as the number of C–Cl bonds increased in the presence of NOM; and（vi） even when the dechlorination reaction was incomplete, it produced chlorophenol. Furthermore, the free radicals of NOM led to the ring-opening reactions of PCBs via an initial addition step. The main site of these ring-opening reactions was the ortho position. Notably, the likelihood of ring-opening reactions occurring involving the degradation products increased as the degradation degree of PCBs increased.
基金supported by the Hi-Tech Research and Development Program(863 Program)of China(No.2002AA302304)the Nationa1 Natura1 Science Foundation of China(No.60121101)the Education Department Foundation of Jiangsu Province(JH01-010).
文摘The cerium ion(Ce4+) doped titania sol and nanocrystallites were prepared by chemical coprecipitation-peptization and hydrothermal synthesis methods, respectively. The X-ray diffraction pattern shows that Ce4+-TiO2 xerogel powder has semicrystalline structure and thermal sintering sample has crystalline structure. Ce4+-TiO2 nanocrystallites are composed of the major anatase phase titania (88.82 wt pct) and a small amount of crystalline cerium titanate. AFM micrograph shows that primary particle size of well-dispersed ultrafine sol particles is below 15 nm in diameter. The particle sizes are 30 nm for xerogel sample and 70 nm for nanocrystallites sample, which is different from the estimated values (2.41 nm and 4.53 nm) by XRD Scherrer's formula. The difference is mainly due to aggregation of nanocrystallites. The experimental results exhibit that photocatalysts of Ce4+-TiO2 sol and nanocrystallites have the ability to photodegrade reactive brilliant red dye (X-3B ) under visible light irradiation with the ion-TiO2/VIS/dye system. Moreover, Ce4+ doped titania sol has shown higher efficiency than the nanocrystallites sample in respect of potocatalytic activity. Meanwhile, dye photodegradation mechanisms are proposed to different photocatalytic reaction systems, which are dye photosensitization, ion-dye photosensitization and interband photocatalysis & dye photosensitization with respect to TiO2 nanocrystallites, Ce4+-TiO2 sol and Ce4+-TiO2 nanocrystallites system.
基金supported by the National Natural Science Foundation of China (Grant Nos. 20976075 and 10972091)College Graduate Student Scientific Research Innovation Foundation of Jiangsu,China (Grant No. CXLX12-0619)
文摘By introducing periodic switching signal associated with illumination to the Originator,a switched mathematical model has been established.The bifurcation sets are derived based on the characteristics of the equilibrium points.Two types of periodic oscillation,such as 2T-focus/cycle periodic switching and 2T-focus/focus periodic switching,have been observed,the mechanism of which is presented through the switching relationship.The distribution of eigenvalues related to the equilibrium points determined by two subsystems is discussed to interpret oscillation-increasing and oscillation-decreasing cascades of the periodic oscillations.Furthermore,the invariant subspaces of the equilibrium point are investigated to reveal the mechanism of dynamical phenomena in the periodic switching.
