COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMS
The copolymerization of styrene with p-methylstyrene has been tested using combined diphenylzinc-additive initiator systems, including diphenylzinc, Ph2Zn, a metallocene: cyclopentadienyltitanium trichloride, CpTiCl3, and methylalumoxane, MAO, as well as the binary CpTiCl3-MAO initiator system. Both combined initiator systems were able to induce S/p-MeS copolymerization and the corresponding homopolymerizations. Conversion to copolymer increases with an increase of p-MeS in the initial feed, while p-MeS homopolymerization led to greater conversion than that of S. From the copolymers obtained using these initiator systems only those produced from S/p-MeS = 95/5 (mol/mol) in the feed showed to be crystalline, with Tm values lower than that of pure s-PS, making them easier to process
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Sociedad Chilena de Química
2002
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oai:scielo:S0366-164420020002000092002-10-14COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMSRABAGLIATI,FRANCO M.CARO,CARLOS J.PEREZ,MONICA A. styrene polymerization copolymerization diphenylzinc metallocenes catalysts stereoregularity tacticity The copolymerization of styrene with p-methylstyrene has been tested using combined diphenylzinc-additive initiator systems, including diphenylzinc, Ph2Zn, a metallocene: cyclopentadienyltitanium trichloride, CpTiCl3, and methylalumoxane, MAO, as well as the binary CpTiCl3-MAO initiator system. Both combined initiator systems were able to induce S/p-MeS copolymerization and the corresponding homopolymerizations. Conversion to copolymer increases with an increase of p-MeS in the initial feed, while p-MeS homopolymerization led to greater conversion than that of S. From the copolymers obtained using these initiator systems only those produced from S/p-MeS = 95/5 (mol/mol) in the feed showed to be crystalline, with Tm values lower than that of pure s-PS, making them easier to processinfo:eu-repo/semantics/openAccessSociedad Chilena de QuímicaBoletín de la Sociedad Chilena de Química v.47 n.2 20022002-06-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0366-16442002000200009en10.4067/S0366-16442002000200009 |
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RABAGLIATI,FRANCO M. CARO,CARLOS J. PEREZ,MONICA A. |
| spellingShingle |
RABAGLIATI,FRANCO M. CARO,CARLOS J. PEREZ,MONICA A. COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMS |
| author_facet |
RABAGLIATI,FRANCO M. CARO,CARLOS J. PEREZ,MONICA A. |
| author_sort |
RABAGLIATI,FRANCO M. |
| title |
COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMS |
| title_short |
COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMS |
| title_full |
COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMS |
| title_fullStr |
COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMS |
| title_full_unstemmed |
COPOLYMERIZATION OF STYRENE BY DIPHENYLZINC-ADDITIVE SYSTEMS: PART III. COPOLYMERIZATION OF STYRENE/para- METHYLSTYRENE USING CpTiCl3-MAO and Ph2Zn-CpTiCl3-MAO INITIATOR SYSTEMS |
| title_sort |
copolymerization of styrene by diphenylzinc-additive systems: part iii. copolymerization of styrene/para- methylstyrene using cpticl3-mao and ph2zn-cpticl3-mao initiator systems |
| description |
The copolymerization of styrene with p-methylstyrene has been tested using combined diphenylzinc-additive initiator systems, including diphenylzinc, Ph2Zn, a metallocene: cyclopentadienyltitanium trichloride, CpTiCl3, and methylalumoxane, MAO, as well as the binary CpTiCl3-MAO initiator system. Both combined initiator systems were able to induce S/p-MeS copolymerization and the corresponding homopolymerizations. Conversion to copolymer increases with an increase of p-MeS in the initial feed, while p-MeS homopolymerization led to greater conversion than that of S. From the copolymers obtained using these initiator systems only those produced from S/p-MeS = 95/5 (mol/mol) in the feed showed to be crystalline, with Tm values lower than that of pure s-PS, making them easier to process |
| publisher |
Sociedad Chilena de Química |
| publishDate |
2002 |
| url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0366-16442002000200009 |
| work_keys_str_mv |
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| _version_ |
1755989215142739968 |