2009
DOI: 10.1134/s0018143909060071
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Radiation synthesis of telomers at a constant tetrafluoroethylene concentration in acetone

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Cited by 20 publications
(6 citation statements)
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“…Radiation-induced telomerization of TFE in solvents leads to the formation of telomers with the common formula R 1 -(TFE) n -R 2 , where n is the chain length, R 1 and R 2 are the end groups representing solvent molecule fragments. When telomers are synthesized in acetone (C 3 H 6 O), the end groups can be H, CH 3 , COCH 3 and CH 2 COCH 3 [38,39], in butyl chloride (CH 3 (CH 2 ) 3 Cl)-H, Cl, and C 4 H 8 Cl [35,40] and in trimethylchlorosilane (C 3 H 9 ClSi)-Cl, -(CH 3 ) 2 ClSi and -(CH 3 ) 3 Si [11,37]. UPTFE FORUM ® does not have such end groups.…”
Section: Introductionmentioning
confidence: 99%
“…Radiation-induced telomerization of TFE in solvents leads to the formation of telomers with the common formula R 1 -(TFE) n -R 2 , where n is the chain length, R 1 and R 2 are the end groups representing solvent molecule fragments. When telomers are synthesized in acetone (C 3 H 6 O), the end groups can be H, CH 3 , COCH 3 and CH 2 COCH 3 [38,39], in butyl chloride (CH 3 (CH 2 ) 3 Cl)-H, Cl, and C 4 H 8 Cl [35,40] and in trimethylchlorosilane (C 3 H 9 ClSi)-Cl, -(CH 3 ) 2 ClSi and -(CH 3 ) 3 Si [11,37]. UPTFE FORUM ® does not have such end groups.…”
Section: Introductionmentioning
confidence: 99%
“…The key factor of the feasibility of this technology is the discovery of the radiation assisted production of low molecular weight polytetrafluoroethylene soluble in organic sol vents. The main results of analyzing this technology and developing the processes for producing the required fractions of tetrafluoroethylene oligomers (telomers) were described in the literature [1][2][3], and the novelty of the technical solution is protected by patents [4,5].…”
mentioning
confidence: 99%
“…Another promising method of making synthetic fabrics waterrepellent is to form a protective coating on their surface by application of tetrafl uoroethylene telomers from solution in acetone [6]. The features of this method and possibility of increasing its effi cacy are examined in the present study.The product based on tetrafl uoroethylene telomers (trade name Cherfl on) was developed and is manufactured at the Institute of Problems in Chemical Physics (IPCP), Russian Academy of Sciences (Chernogolovka) using radiochemical initiation of polymerization of tetrafl uoroethylene monomers ( 60 Co  radiation) [7][8][9]. A mixture of telomers containing more than 90% molecules with an average degree of polymerization of 5-6 and CH 3 -C=O-CH 2 -end groups is formed as a result [7].…”
mentioning
confidence: 99%
“…The product based on tetrafl uoroethylene telomers (trade name Cherfl on) was developed and is manufactured at the Institute of Problems in Chemical Physics (IPCP), Russian Academy of Sciences (Chernogolovka) using radiochemical initiation of polymerization of tetrafl uoroethylene monomers ( 60 Co  radiation) [7][8][9]. A mixture of telomers containing more than 90% molecules with an average degree of polymerization of 5-6 and CH 3 -C=O-CH 2 -end groups is formed as a result [7].…”
mentioning
confidence: 99%
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