Show simple item record

dc.contributor.advisorPeranginangin, Sabarmin
dc.contributor.authorHutajulu, Cicilia Agustin
dc.date.accessioned2023-05-18T07:13:31Z
dc.date.available2023-05-18T07:13:31Z
dc.date.issued2023
dc.identifier.urihttps://repositori.usu.ac.id/handle/123456789/84770
dc.description.abstractSynthesis of cardanyl methyl ether was carried out through an etherification reaction between cardanol isolated from the shell of cashew nuts (Anacardium occidentale L.) and methyl iodide. Cardanol isolation was carried out by adding acetone, Ca(OH)2, 25% NH4OH, n-hexane: ethyl acetate (98:2), washing with 2.5% NaOH, 5% HCl, distilled water and then adding anhydrous Na2SO4. The yield of cardanol was 74.39 g (74.39% of the initial weight of CNSL) with a characteristic acid number of 1.2863 mgKOH/g, iodine number of 215.6535 g I2/100 g, viscosity of 38.7 Cp, density of 0.8266 g/m, pH 6.14. Cardanyl methyl ether was synthesized by adding K2CO3, acetone and methyl iodide with a reflux time of 8 hours. The parameters used in this study were reflux time variations (7 hours, 8 hours, 9 hours) and yielded 7,646 g; 12,084 g; 5,276 g cardanyl methyl ether. The obtained Cardanol and Cardanyl methyl ether were analyzed by FT-IR and GC-MS spectrophotometer. FT-IR analysis showed the formation of cardanol and cardanyl methyl ether which was characterized by the difference in the peaks of the stretching vibrations of the C-O group and the stretching vibrations of the C-O-C groups at wave numbers 1300-1000 cm-1 whereas in the isolated CNSL cardanol was characterized by the presence of stretching vibrations of the C-O group in wave number 1162.9 cm-1 , whereas in cardanyl methyl ether it is characterized by the presence of stretching vibrations of the C-O group at wave numbers 1162.9-1259.8 cm-1 and stretching vibrations of the C-O-C group at wave numbers 1043.6-1148.0 cm-1 . GC-MS analysis showed that the proportion of cardanol obtained was 63.28%, and the proportion of cardanyl methyl ether with variations in reflux time (7 hours, 8 hours, 9 hours) was obtained at 30.18%, 30.29% and 22.09 %. The results of the analysis showed that the maximum proportion of cardanyl methyl ether was obtained under the molar reaction conditions of cardanol: methyl iodide (1:3), K2CO3 17.3 g, acetone 50 mL, with reflux time of 8 hoursen_US
dc.language.isoiden_US
dc.publisherUniversitas Sumatera Utaraen_US
dc.subjectCardanolen_US
dc.subjectCardanyl Methyl Etheren_US
dc.subjectEtherificationen_US
dc.subjectMethyl Iodideen_US
dc.titleSintesis Kardanil Metil Eter melalui Reaksi Eterifikasi Kardanol Hasil Isolasi Kulit Biji Jambu Mete (Anacardium occidentale L.) dengan Metil Iodida pada Variasi Waktuen_US
dc.typeThesisen_US
dc.identifier.nimNIM180802052
dc.identifier.nidnNIDN0013126905
dc.identifier.kodeprodiKODEPRODI47201#Kimia
dc.description.pages83 Halamanen_US
dc.description.typeSkripsi Sarjanaen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record