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Dilute Ionic Liquids Pretreatment of Palm Empty Bunch and Its Impact to Produce Bioethanol Arianie, Lucy; Pebriyana, Utin Dewi; Yudiansyah, Yudiansyah; Idiawati, Nora; Wahyuningrum, Deana
The Journal of Pure and Applied Chemistry Research Vol. 3 No. 2 (2014)
Publisher : Chemistry Department, The University of Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1355.056 KB) | DOI: 10.21776/ub.jpacr.%y.03.02.165

Abstract

Ethanol production through ionic liquids pretreatment of palm empty bunch (PEB) was carried out. This research aims to investigate impact of ionic liquids synthetic i.e 1-butyl-3-methyl imidazoliumbromide or [BMIM]bromide toward cellulose’s palm empty bunch and convert its cellulose into bioethanol. Ionic liquid was synthesized  through reflux and microwave assisted synthesis methods. Research investigation showed that microwave assisted synthesis produce [BMIM]bromide 90% faster than reflux method. The characterization of synthesized product using FTIR, 1H-NMR, 13C-NMR and LC-MS showed that these reactions have been carried out successfully. Scanning electron microscope figure out changes morphological surface of palm empty bunch caused by ionic liquid pretreatment. Crystallinity index of PEB milled and cellulose of PEFB after [BMIM]bromide dissolution were identified using comparison of PEB FTIR spectrum. Cellulose without dilute [BMIM]bromide have higher LOI number than cellulose after [BMIM]bromide dissolution. It indicated that a large part of cellulose after dissolution has been changed into amorf. Hydrolysis residue of palm empty bunch hydrolyzed by sulfuric acids 5%, 100 0C for 5 hours and produce 685 ppm of reducing sugar. Simultaneous Saccharification and Fermentation using Trichoderma viride and Saccharomyce cerevisiae  for 5 days produce 0,69% of bioethanol.
Synthesis, Characterization, and Micellar Behavior of Amphiphilic Chitosan Bearing Sulfate and Anisaldehyde Imine Groups Herayati Herayati; Deana Wahyuningrum; Damar Nurwahyu Bima; Indah Puspita Sari
Biology, Medicine, & Natural Product Chemistry Vol 14, No 2 (2025)
Publisher : Sunan Kalijaga State Islamic University & Society for Indonesian Biodiversity

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14421/biomedich.2025.142.905-909

Abstract

Amphiphilic chitosan derivatives bearing sulfate and anisaldehyde imine (anisimine) groups were successfully synthesized and characterized for potential applications as functional biomaterials. The synthesis involved two key steps: (1) sulfation of chitosan using chlorosulfonic acid to introduce O-sulfate groups, and (2) Schiff base formation via reaction with p-anisaldehyde to generate N-anisimine functionalities. Structural modifications were confirmed by Fourier-transform infrared (FTIR) spectroscopy, which showed characteristic absorption bands at ~1250 cm-¹ and ~820 cm-¹ corresponding to O=S=O stretching of sulfate, and a C=N stretch at ~1640 cm-¹ indicating imine formation. Proton nuclear magnetic resonance (1H-NMR) spectra further verified the successful attachment of aromatic protons from p-anisaldehyde and the disappearance of primary amine peaks, confirming imination. The amphiphilic behavior and micelle-forming ability of the N-anisimine-O-sulfated (NAOS) chitosan were evaluated using pyrene as a hydrophobic fluorescent probe for determining the critical micelle concentration (CMC), which was found to be 0.012 mg/mL. The observed low CMC value indicates strong self-assembly capability in aqueous media. These results suggest that NAOS chitosan possesses promising structural and surface-active properties suitable for advanced applications in drug delivery and cosmetic formulations.