PREPARATION OF ARYLSULFONE DERIVATIVE OF POLYSTYRENE WITH P-TOLUENE SULFONYL CHLORIDE
| dc.contributor.author | CANSIZ, A | |
| dc.contributor.author | COSKUN, M | |
| dc.contributor.author | OZDEMIR, E | |
| dc.date.accessioned | 2026-08-12T16:34:02Z | |
| dc.date.issued | 1991 | |
| dc.department | Fırat Üniversitesi | |
| dc.description.abstract | The arylsulfone derivative of polystyrene was prepared by p-toluene sulfonyl chloride in the presence of anhydrous aluminum chloride in methylene chloride at three different temperatures. The sulfonated polystyrenes were characterized by IR spectrophotometer, H-1-NMR spectrometer and sulfur analyzer. Activation energy of the sulfonation reaction was found to be 38,0 kj mol-1 and 36,5 kj mol-1 from the results of HCl and sulfur determinations, respectively. Solubility parameters and densities of some sulfonated polystyrenes were also determinated. | |
| dc.identifier.doi | 10.1080/00222339108054395 | |
| dc.identifier.endpage | 150 | |
| dc.identifier.issn | 0022-233X | |
| dc.identifier.orcid | 0000-0002-3692-6740 | |
| dc.identifier.scopus | 2-s2.0-0026173071 | |
| dc.identifier.scopusquality | N/A | |
| dc.identifier.startpage | 143 | |
| dc.identifier.uri | https://doi.org/10.1080/00222339108054395 | |
| dc.identifier.uri | https://hdl.handle.net/11508/44265 | |
| dc.identifier.volume | A28 | |
| dc.identifier.wos | WOS:A1991FZ04600008 | |
| dc.identifier.wosquality | N/A | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Marcel Dekker Inc | |
| dc.relation.ispartof | Journal of Macromolecular Science-Chemistry | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WoS_20260511 | |
| dc.subject | Halogenated Polymers | |
| dc.subject | Stability | |
| dc.title | PREPARATION OF ARYLSULFONE DERIVATIVE OF POLYSTYRENE WITH P-TOLUENE SULFONYL CHLORIDE | |
| dc.type | Article |







