Dicyclopentadiene was polymerized by reaction injection molding (RIM) using a catalyst system based on molybdenum (V) chloride and anhydrous aluminum chloride and triethylaluminum. The effect of the reaction temperatu...Dicyclopentadiene was polymerized by reaction injection molding (RIM) using a catalyst system based on molybdenum (V) chloride and anhydrous aluminum chloride and triethylaluminum. The effect of the reaction temperature on the polymer network and the type of the polymerization were discussed.展开更多
Diels-Alder addition of dicyclopentadiene and cyclopentadiene in polar solvents has been studied to produce tricyclopentadiene（TCPD） that is a potential high-density fuel precursor. GC and MS analysis shows that the...Diels-Alder addition of dicyclopentadiene and cyclopentadiene in polar solvents has been studied to produce tricyclopentadiene（TCPD） that is a potential high-density fuel precursor. GC and MS analysis shows that the adducts contain two isomers, namely exo- and endo-TCPD. Theoretical simulation shows that although the transition state of endo-TCPD has a lower activation energy, exo-TCPD is thermodynamically preferred. Polar solvents can accelerate the reaction rate and improve the exo/endo ratio of TCPD because the transition state of exo-TCPD has a higher polarity than that of endo-TCPD. The solvent effect follows the order of polarity： benzyl methanol〉cyclohexanone〉toluene. The conversion rises when the temperature ranges from 120 to 150 ℃, but the selectivity of TCPD slightly decreases. Increasing the pressure can improve the conversion but the exo/endo ratio of TCPD is unchanged. The apparent kinetics in different solvents was determined via nonlinear regression. The activation energies are 99.47, 101.15, and 107.32 kJ/mol for benzyl methanol, cyclohexanone, and toluene, respectively. The optimal reaction conditions are as follows： benzyl methanol as solvent, temperature 150 ℃, and pressure 900 kPa. After an 11-hour reaction, a conversion of 58.0%, a TCPD selectivity of 95.7%, and an exo/endo ratio of 1/5.3 has been obtained.展开更多
The copolymerization of ethylene with dieyclopentadiene （DCP） in the presence of a constrained geometry tetramethylcyclopentadi-enyl-phenoxytitanium catalyst [ 2,4-＇ Bu2-6-（ 2,3,4,5-Me4 -Cp ） -PhO ] TICl2, combin...The copolymerization of ethylene with dieyclopentadiene （DCP） in the presence of a constrained geometry tetramethylcyclopentadi-enyl-phenoxytitanium catalyst [ 2,4-＇ Bu2-6-（ 2,3,4,5-Me4 -Cp ） -PhO ] TICl2, combined with AI（ iBu）3/Ph3C^＋ B（ CsF5 ）4^- cocatalyst system was studied. The copolymers that were formed were characterized by ＇ H and ,3 C NMR, differential scanning calorimetry （ DSC）, SEM, and X-ray diffraction （XRD） analyses. The re- suits of the analysis indicate that the copolymers of ethylene with dicyclopentadiene are amorphous and display two or more melting temperatures in their DSC diagrams. Moreover, the morphologies of the copolymers are quite different from that of polyethylenes.展开更多
The complexes of cyclopentadienyl tetramethylethenebridsied dicyclopentadienylsamarium (Ⅲ) tetrahydrofuranates, Me4C2(C5H4)2LnC5H5 (THF) (Ln = Nd, Sm, Gd, Yb) were synthesized and characterized by elemental analysis,...The complexes of cyclopentadienyl tetramethylethenebridsied dicyclopentadienylsamarium (Ⅲ) tetrahydrofuranates, Me4C2(C5H4)2LnC5H5 (THF) (Ln = Nd, Sm, Gd, Yb) were synthesized and characterized by elemental analysis, IR, 1HNMR, thermogravimetry and MS. The crystal structure of Me4C2(C5H4)2SmC5H5 was determined by X-ray diffraction method. The crystal belongs orthorhombic space group Cc2a. with a =1 . 1696(6) nm, b =1 .2539(5) nm, c = 2.9432(15) nm, V= 4.316 (4) nm3, Z= 8 and Dc = 1 . 54 g . cm-3.展开更多
文摘Dicyclopentadiene was polymerized by reaction injection molding (RIM) using a catalyst system based on molybdenum (V) chloride and anhydrous aluminum chloride and triethylaluminum. The effect of the reaction temperature on the polymer network and the type of the polymerization were discussed.
基金Supported by Fundamental Research Project of Commission of ScienceTechnology and Industry for National Defense of China(NoA1420060192)
文摘Diels-Alder addition of dicyclopentadiene and cyclopentadiene in polar solvents has been studied to produce tricyclopentadiene（TCPD） that is a potential high-density fuel precursor. GC and MS analysis shows that the adducts contain two isomers, namely exo- and endo-TCPD. Theoretical simulation shows that although the transition state of endo-TCPD has a lower activation energy, exo-TCPD is thermodynamically preferred. Polar solvents can accelerate the reaction rate and improve the exo/endo ratio of TCPD because the transition state of exo-TCPD has a higher polarity than that of endo-TCPD. The solvent effect follows the order of polarity： benzyl methanol〉cyclohexanone〉toluene. The conversion rises when the temperature ranges from 120 to 150 ℃, but the selectivity of TCPD slightly decreases. Increasing the pressure can improve the conversion but the exo/endo ratio of TCPD is unchanged. The apparent kinetics in different solvents was determined via nonlinear regression. The activation energies are 99.47, 101.15, and 107.32 kJ/mol for benzyl methanol, cyclohexanone, and toluene, respectively. The optimal reaction conditions are as follows： benzyl methanol as solvent, temperature 150 ℃, and pressure 900 kPa. After an 11-hour reaction, a conversion of 58.0%, a TCPD selectivity of 95.7%, and an exo/endo ratio of 1/5.3 has been obtained.
基金Supported by the National Natural Science Foundation of China(Nos 20674024 and 20374023)
文摘The copolymerization of ethylene with dieyclopentadiene （DCP） in the presence of a constrained geometry tetramethylcyclopentadi-enyl-phenoxytitanium catalyst [ 2,4-＇ Bu2-6-（ 2,3,4,5-Me4 -Cp ） -PhO ] TICl2, combined with AI（ iBu）3/Ph3C^＋ B（ CsF5 ）4^- cocatalyst system was studied. The copolymers that were formed were characterized by ＇ H and ,3 C NMR, differential scanning calorimetry （ DSC）, SEM, and X-ray diffraction （XRD） analyses. The re- suits of the analysis indicate that the copolymers of ethylene with dicyclopentadiene are amorphous and display two or more melting temperatures in their DSC diagrams. Moreover, the morphologies of the copolymers are quite different from that of polyethylenes.
文摘The complexes of cyclopentadienyl tetramethylethenebridsied dicyclopentadienylsamarium (Ⅲ) tetrahydrofuranates, Me4C2(C5H4)2LnC5H5 (THF) (Ln = Nd, Sm, Gd, Yb) were synthesized and characterized by elemental analysis, IR, 1HNMR, thermogravimetry and MS. The crystal structure of Me4C2(C5H4)2SmC5H5 was determined by X-ray diffraction method. The crystal belongs orthorhombic space group Cc2a. with a =1 . 1696(6) nm, b =1 .2539(5) nm, c = 2.9432(15) nm, V= 4.316 (4) nm3, Z= 8 and Dc = 1 . 54 g . cm-3.
