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dc.contributor.advisorKaban, Jamaran
dc.contributor.advisorGinting, Adil
dc.contributor.authorIrwansyah
dc.date.accessioned2021-09-02T01:59:49Z
dc.date.available2021-09-02T01:59:49Z
dc.date.issued2011
dc.identifier.urihttp://repositori.usu.ac.id/handle/123456789/42064
dc.description.abstractMany researchers interest to develope using of chitosan by performing chemical transformation reaction to produce chitosan derivatives. It has been conducted formation of N-palmityl chitosan from the reaction between palmityl chloride and chitosan. Palmityl chloride was produced by reaction between palmatic acid with phosphorpentachloride in chloroform at (60-70) oC for 3 hours. Palmityl chloride was reacted with chitosan in chloroform at 0 oC for 30 minutes, then it was hydrolyzed by using NaOH 1M at (60-65) oC for 20 hours. Formation of N-palmityl chitosan can be seen from FT-IR analysis, where absorptions at 2916 cm-1 (alkyl group, CH- stratching, CH3- assymetris), 2848 cm-1 (alkyl group, CH- stretching, -CH2- symetris), 720 cm-1 (-CH2- rocking in C-(CH2)n-C), 3448 cm-1 (amide, N-H stretching, R2NH secondary, and –OH stretching, dimer), 1543 cm-1 (amide-II, N-H deformation, secondary), 1573 cm-1 (amide-I, NH stretching, C=O stretching, secunder) and 1111 cm-1 (amide-III, CN stretching-NH deformation, secondary).en_US
dc.description.abstractBanyak peneliti tertarik untuk mengembangkan kegunaan kitosan dengan melakukan reaksi transformasi kimia menjadi turunan kitosan. Telah dilakukan pembuatan N-palmitil kitosan dari reaksi antara palmitil klorida dengan kitosan. Palmitil klorida diperoleh melalui reaksi antara asam palmitat dengan phosforpentaklorida dalam pelarut kloroform pada suhu 60 – 70 oC selama 3 jam. Palmitil klorida direaksikan dengan kitosan dalam kloroform pada suhu O oC selama 30 menit, lalu dihidrolisis menggunakan NaOH 1 M pada suhu 60 – 65 oC selama 20 jam. Terbentuknya N-palmitil kitosan dapat dilihat dari hasil analisa FT-IR, dimana muncul serapan 2916 cm-1 (gugus alkil, CH- stratching; CH3- asymetris), 2848 cm-1 (gugus alkil, CH- stretching; -CH2- symetris), 720 cm-1 (-CH2- rocking in C-(CH2)n-C), 3448 cm-1 (amida, N-H stretching; NH sekunder, dan –OH stretching; dimer), 1543 cm-1(amida II, N-H deformasi; sekunder), 1573 cm-1 (amida I, N-H stretching; C=O stretching; sekunder) dan 1111 cm-1 (amida III, CN stretching-NH deformation, sekunder).en_US
dc.language.isoiden_US
dc.publisherUniversitas Sumatera Utaraen_US
dc.subjectN-Palmitil Kitosanen_US
dc.subjectKitosanen_US
dc.subjectAsam Palmitaten_US
dc.subjectPalmitil Kloridaen_US
dc.subjectFT- IRen_US
dc.titleTransformasi Kitosan dan Asam Palmitat Menjadi N-Palmitil Kitosanen_US
dc.typeThesisen_US
dc.identifier.nimNIM097006032
dc.description.pages76 Halamanen_US
dc.description.typeTesis Magisteren_US


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