Daniel Daniel
Jurusan Kimia FMIPA Universitas Mulawarman

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PROFIL TUMBUHAN SIKKAM (Bischovia javanica Blume) Karolina Sinukaban; Chairul Saleh; Daniel Daniel
PROSIDING SEMINAR KIMIA SEMINAR NASIONAL KIMIA 2019
Publisher : PROSIDING SEMINAR KIMIA

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Abstract

Penelitian tentang uji toksisitas dan uji aktivitas antioksidan ekstrak kulit batang tumbuhan sikkam (Bischovia javanica Blume) telah dilakukan. Hasil dari uji fitokimia pada kulit batang tumbuhan sikkam mengandung senyawa metabolit sekunder yaitu senyawa fenolik, flavonoid dan triterpenoid. Berdasarkan hasil uji toksisitas dengan metode BSLT (Brine Shrimp Lethality Test) pada ekstrak kasar metanol diperoleh nilai LC50 sebesar 56,92 ppm yang menunjukkan tingkat toksisitas yang toksit sehingga dapat dimanfaatkan sebagai obat antikanker. Berdasarkan hasil uji aktivitas antioksidan dengan metode DPPH menunjukkan pada ekstrak kasar metanol diperoleh nilai IC50 sebesar 9,1878 ppm. Dari hasil uji antioksidan diketahui bahwa pada ekstrak kasar metanol kulit batang tumbuhan sikkam memiliki aktivitas antioksidan yang sangat kuat dengan nilai IC50 sebesar 9,1878 ppm. Kata Kunci: Sikkam (Bischofia javanica Blume), Uji Fitokimia, Uji Toksisitas, Uji Aktivitas Antioksidan, DPPH (1,1-diphenyl-2-picrylhidrazyl)
PEMBUATAN SURFAKTAN BERBAHAN DASAR MINYAK BIJI MAHONI Swietenia macrophylla King DENGAN DIETANOLAMINA Catur Oktaviani; Daniel Daniel
JURNAL KIMIA MULAWARMAN Vol 17 No 2 (2020)
Publisher : Jurusan Kimia Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Mulawarman

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30872/jkm.v17i2.692

Abstract

ABSTRACT This research was conducted to synthesize diethanolamide synthesis from methyl esters of mahogany seed oil (Swietenia macrophylla King) trough an oxidation reaction with variation in catalyst weight. The results showed that the 48,97% mahogany seed oil content of acid was 24,239 mg KOH/g. The mahogany seed oil was methyl ester through the reverse asterification method 0f 0,791 mg KOH/g, saponification is 88,373 mg KOH/g. The results of the GC-MS analysis of the dominant fatty acid are methyl linoleic by 36,02%. Methyl esters are reacted with diethanolamine through an amidation method using a variation of catalyst weight which is 0,5%, 1% and 1,5% with yield percentages of 71,197%, 79,638% and 82,035%. The optimum condition of diethanolamide synthesis is the catalyst weight variation of 1.5% which can reduce water surface tension by 45,159%. The FT-IR spectrum data shows that the absorption peak which is specific to the amide group is found at wave number 1620cm-1 so it can be concluded that the compound is diethanolamide. Keyword : Mahogany seed oil, esterification amidation, diethanolamide. ABSTRAK Penelitian ini dilakukan untuk mensintesis dietanolamida dari metil ester minyak biji mahoni (Swietenia machrophylla King) melalui reaksi amidasi dengan variasi berat katalis. Hasil penelitian menunjukkan kandungan minyak biji mahoni 48,97% bilangan asam sebesar 24,239 mg KOH/g minyak biji mahoni tersebut dikonversi menjadi metil ester melalui metode esterifikasi menurunkan bilangan asam sebesar 0,791 mg KOH/g, bilangan penyabunan adalah 88,373 mg KOH/g. Hasil dari analisa GC-MS asam lemak yang dominan yaitu metil linoleat sebesar 36,02%. Metil ester direaksikan dengan dietanolamina melalui metode amidasi dengan menggunakan variasi berat katalis yaitu 0,5%, 1% dan 1,5% dengan persen rendemen sebesar 71,197%, 79,638% and 82,035%. Kondisi optimum dari sintesis dietanolamida yaitu pada variasi berat katalis 1,5% yang dapat menurunkan tegangan permukaan air sebesar 45,159%. Hasil data spektrum FT-IR menunjukkan puncak serapan yang spesifik untuk gugus amida terdapat pada bilangan gelombang 1620 cm-1 sehingga dapat disimpulkan bahwa senyawa tersebut adalah dietanolamida. Kata Kunci : Minyak biji mahoni, esterifikasi, amidasi, dietanolamida
SINTESIS SURFAKTAN DIETANOLAMIDA DARI METIL ESTER MINYAK BIJI BUNGA MATAHARI (Helianthus annuus. L) MELALUI REAKSI AMIDASI Nur Khasanah; Daniel Daniel; Eva Marliana
JURNAL KIMIA MULAWARMAN Vol 17 No 2 (2020)
Publisher : Jurusan Kimia Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Mulawarman

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.30872/jkm.v17i2.708

Abstract

Synthesis of dietanolamide surfactant from methyl ester of sunflower seed oil (Helianthus annuus. L) has been carried out through an amidation reaction. In the extraction process showed the oil content of sunflower seeds was 32.93% with an acid number of 3.25 mg KOH/g and ALB levels of 1.63%. Sunflower seed oil was then converted to methyl ester through the esterification process and obtained an acid number 1.84 mg KOH/g so that the ALB level dropped to 0.92% and obtained saponification numbers of 61.19 mg KOH/g. The most dominant composition of methyl ester of sunflower seed oil based on GC-MS analysis was methyl oleate at 23.28%. The FT-IR methyl ester spectrum gives a specific absorption peak for group C=O ester at wave number 1743 cm-1. Methyl esters are converted to diethanolamide through an amidation process. The resulting diethanolamide has an acid number of 9.7 mg KOH/g and a saponification number of 3.08 mg KOH/g. The FT-IR spectrum provides specific absorption peaks for groups C=O amides at wave numbers 1622 cm-1. The value of HLB dietanolamide in practice is 13.6495 and in theory is 14.291 which includes the surfactant in the oil in water (O/W) emulsifying class. Keyword : sunflower seed oil, esterification, amidation, dietanolamide