HPMug2oMmNrOfxWQHLiEksa6s0hFu9Ox348d7QefarYlaFR5ArkhOwm3Da1pmxmxCtenj1+6luWD#r#n+EPn9L6Ce+9onqnMlT+i ›› 2011, Vol. 27 ›› Issue (1): 27-30.DOI: 10.3969/j.issn.1009-0479.2011.01.007
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Abstract: Polyanilinenanofibersdopedbyasuchacidsassulfuricacid,hydrochloricacid,nitricacid andchloroaceticacidwerepreparedbyusingrapidmixturemethod.Scanningelectronmicroscopyanaly sisshowedthatwhenthediameterofpolyanilinefiberwasin50~200nm,acidtypehadlittleeffecton morphologies.Theesterificationofterpineolandaceticanhydridewasregardedasthegoalreactionto studyeffectsofpreparationconditionsoncatalyticactivity.Theresultsprovedthattheyieldofterpinyl acetatereachedthemaxvalue,whichamountedto86.74%.Whennitricacidwasdoped,itsmolarcon centrationwas1.0mol/L,anilinemolarconcentrationwas0.4mol/L,andtheconcentrationratioofam moniumpersulfateandanilinemolarwas1∶4.Undersamereactionconditions,conversionrateofterpine olwas99.50% andesterificationyieldreached86.74%.
Key words: terpineol, polyanilinenanofibers, preparation, esterification
CLC Number:
TQ032.41
ZHENG Xiao-Ying-a, ZHANG Run-Hu-a, TAN Xiang-Dong-b. PreparationandEsterificationPropertiesofPolyanilineNanofibers[J]. HPMug2oMmNrOfxWQHLiEksa6s0hFu9Ox348d7QefarYlaFR5ArkhOwm3Da1pmxmxCtenj1+6luWD#r#n+EPn9L6Ce+9onqnMlT+i, 2011, 27(1): 27-30.
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URL: http://kmyzxb.magtech.com.cn/EN/10.3969/j.issn.1009-0479.2011.01.007
http://kmyzxb.magtech.com.cn/EN/Y2011/V27/I1/27