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Sintesis dan Karakterisasi Surfaktan Dietanolamida dari Minyak Goreng Bekas Terkatalsis CaO/Zeolit

WARNI LUSIANA, Prof. Dr.rer.nat. Karna Wijaya, M.Eng ; Dra. Ani Setyopratiwi, M.Si.

2017 | Skripsi | S1 KIMIA

Telah dilakukan sintesis surfaktan dietanolamida terkatalisis CaO/zeolit dari minyak goreng bekas sebagai surfaktan nonionik. Tujuan dari penelitian ini adalah melakukan preparasi dan karakterisasi katalis CaO/zeolit, mensintesis surfaktan dietanolamida dari minyak goreng bekas terkatalisis CaO/zeolit dengan mengkaji pengaruh konsentrasi CaO yang diembankan ke zeolit untuk sintesis surfaktan dietanolamida. Sintesis katalis CaO/zeolit dilakukan menggunakan metode impregnasi basah dengan variasi konsentrasi CaO 3%, 5% dan 7% (b/b). Katalis dikarakterisasi dengan Fourier Transform InfraRed (FT-IR) dan X-Ray Diffraction (XRD). Tahapan sintesis surfaktan dietanolamida melibatkan reaksi transesterifikasi antara minyak goreng bekas dengan metanol terkatalisis KOH 1% dan reaksi amidasi antara metil ester dengan dietanolamina terkatalis CaO/zeolit. Metil ester hasil transesterifikasi dikarakterisasi dengan Gas Chromatography Mass Spectrometry (GC-MS) dan FT-IR, sedangkan hasil surfaktan dietanolamida dianalisis kestabilan emulsinya, kestabilan busa, penurunan tegangan muka, Konsentrasi Kritis Misel (KKM) dan nilai Hydrofilic-Lypofilic Balance (HLB) serta dikarakterisasi dengan FT-IR. Reaksi transesterifikasi minyak goreng bekas menghasilkan campuran metil ester dengan rendemen 91,20%, sedangkan reaksi amidasi pembentukan surfaktan dietanolamida untuk variasi konsentrasi CaO yang diembankan 3%, 5% dan 7% diperoleh rendemen sebesar 64,47%; 92,91%; dan 87,05%. Hasil karakterisasi surfaktan menunjukkan bahwa semakin tinggi konsentrasi surfaktan, kemampuan menurunkan tegangan muka juga semakin besar, busa yang terbentuk cukup stabil selama 1 jam, indeks emulsi campuran air-surfaktan-pertalite 67% dan pembentukan emulsi stabil hingga 4 hari. Nilai KKM sebesar 1,5 g/L dan HLB surfaktan sebesar 10,59 sehingga surfaktan dapat dimanfaatkan sebagai larutan pembersih dan pelarut.

Synthesis of diethanolamide surfactant catalyzed by CaO/zeolite from used cooking oil as nonionic surfactant has been carried out. The aims of this study were to prepare and characterize of CaO/zeolite catalyst and to synthesize of diethanolamide surfactant from used cooking oil catalyzed by CaO/zeolite with investigate effect of CaO concentration assayed to zeolite for it. Synthesis of CaO/zeolite catalyst was performed using wet impregnation method with various concentrations of CaO were 3%, 5% and 7% (w/w). The catalyst characterized by Fourier Transform InfraRed (FT-IR) and X-Ray Diffraction (XRD). Synthesis steps of the diethanolamide surfactant involved transesterification between cooking used oil with methanol catalyzed by KOH 1% and amidation reaction between methyl ester with diethanolamine catalyzed by CaO/zeolite. Methyl ester from transesterification characterized by Gas Chromatography Mass Spectrometry (GC-MS) and FT-IR, while surfactant diethanolamide was analyzed for the emulsion stability, foam stability, surface tension, Critical Micelle Concentration (CMC) and Hydrofilic-Lypofilic Balance (HLB) value and characterized by FT-IR. Used cooking oil produced of mixture methyl ester from transesterification reaction of with yield of 91.20%, while amidation reaction of surfactant diethanolamide for variation of CaO concentration were 3%, 5% and 7% produced yield were 64.47; 92.91; and 87.05%. The surfactant characterization showed that higher surfactant concentration, the greater surface tension decrease, foam formed was stable until 1 hour, water-surfactant-pertalite system has 67% emulsion index and the stabilized emulsion up to 4 days. The CMC value is 1.5 g/L and HLB value was 10.59 so that the surfactant can be used as cleaner solution and solvent.

Kata Kunci : dietanolamida, katalis CaO/zeolit, minyak goreng bekas, surfaktan, amidasi

  1. S1-2017-347427-abstract.pdf  
  2. S1-2017-347427-bibliography.pdf  
  3. S1-2017-347427-tableofcontent.pdf  
  4. S1-2017-347427-title.pdf