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Sequential Microwave-Ultrasound Assisted Extraction of Flavonoid from Moringa oleifera: Product Characteristic, Antioxidant and Antibacterial Activity Aji Prasetyaningrum; Bakti Jos; Ratnawati Ratnawati; Nur Rokhati; Teguh Riyanto; Gian Restu Prinanda
Indonesian Journal of Chemistry Vol 22, No 2 (2022)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.65252

Abstract

Moringa oleifera leaves contain secondary metabolites in flavonoid compounds known to prevent several diseases. Therefore, appropriate extraction methods are required to produce extracts with a high yield of flavonoids from Moringa. In this study, the extraction from Moringa leaves was carried out using the sequential microwave/ultrasound-assisted extraction (MUAE) method compared with sequential ultrasound/microwave (UMAE), microwave (MAE), ultrasound (UAE), and maceration (ME). The effects of the time, temperature, and percentage of ethanol were studied on total flavonoid content using AlCl3 colorimetric assay. The extracts were analyzed by Scanning Electron Microscopy (SEM), Fourier Transforms Infrared Spectrophotometry (FTIR), and High-Performance Liquid Chromatography (HPLC). The antioxidant and antibacterial activities were tested using DPPH-scavenging and disc diffusion methods. The results of SEM surface analysis on various extraction methods show differences on each surface. The FTIR spectrum showed the presence of flavonoid O–H at 3200 cm–1, C=O at 1621 cm–1, and C–O at 1019 cm–1. In the results of HPLC, MUAE extracts 16.70 mg/ 100 g flavonoid quercetin at the retention time of 4.5 min, with the highest total flavonoids (2.89 mg QE/g), the highest antioxidant activity (IC50 72.31 µg/mL), and highest antibacterial activity (S. aureus 7 mm, E. coli 2 mm).
Bifunctional CaCO3/HY Catalyst in the Simultaneous Cracking-Deoxygenation of Palm Oil to Diesel-Range Hydrocarbons Rosyad Adrian Febriansyar; Teguh Riyanto; I. Istadi; Didi D. Anggoro; Bunjerd Jongsomjit
Indonesian Journal of Science and Technology Vol 8, No 2 (2023): (ONLINE FIRST) IJOST: September 2023
Publisher : Universitas Pendidikan Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.17509/ijost.v8i2.55494

Abstract

Palm oil is a promising raw material for biofuel production using the simultaneous catalytic mechanism of the bifunctional cracking-deoxygenation reactions. Through the cracking-deoxygenation process, the chains of palmitic acid and oleic acid in the palm oil were converted to diesel-range hydrocarbons. The combination effects of CaCO3 and HY zeolite enhanced the bifunctional catalytic cracking-deoxygenation of palm oil into biofuel, because of the increasing acid and basic sites in the catalysts due to the synergistic roles of CaCO3 and HY. The introduction of CaCO3 on HY zeolite generated both a strong acid and strong basic sites simultaneously on the designed catalyst, which supports the bifunctional mechanisms of hybrid cracking-deoxygenation, respectively. The CaCO3 impregnated on the HY catalyst has a synergistic and bifunctional effect on the catalyst supporting cracking-deoxygenation reaction mechanisms as mentioned previously. The deoxygenation reaction required the bifunctional strong acid and strong basic sites on the CaCO3/HY catalyst through decarboxylation, decarbonylation, and hydrodeoxygenation reaction mechanisms. Meanwhile, the cracking reaction pathway was supported by the strong acid sites generated on the CaCO3/HY catalyst. In other words, the high acidity strength promotes diesel selectivity, whereas the high strength of basicity leads to the deoxygenation reaction.
Biofuels Production from Catalytic Cracking of Palm Oil Using Modified HY Zeolite Catalysts over A Continuous Fixed Bed Catalytic Reactor I. Istadi; Teguh Riyanto; Luqman Buchori; Didi D. Anggoro; Andre W. S. Pakpahan; Agnes J. Pakpahan
International Journal of Renewable Energy Development Vol 10, No 1 (2021): February 2021
Publisher : Center of Biomass & Renewable Energy, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/ijred.2021.33281

Abstract

The increase in energy demand led to the challenging of alternative fuel development. Biofuels from palm oil through catalytic cracking appear as a promising alternative fuel. In this study, biofuel was produced from palm oil through catalytic cracking using the modified HY zeolite catalysts. The Ni and Co metals were impregnated on the HY catalyst through the wet-impregnation method. The catalysts were characterized using X-ray fluorescence, X-ray diffraction, Brunauer–Emmett–Teller (BET), Pyridine-probed Fourier-transform infrared (FTIR) spectroscopy, and Scanning Electron Microscopy (SEM) methods. The biofuels product obtained was analyzed using a gas chromatography-mass spectrometry (GC-MS) method to determine its composition. The metal impregnation on the HY catalyst could modify the acid site composition (Lewis and Brønsted acid sites), which had significant roles in the palm oil cracking to biofuels. Ni impregnation on HY zeolite led to the high cracking activity, while the Co impregnation led to the high deoxygenation activity. Interestingly, the co-impregnation of Ni and Co on HY catalyst could increase the catalyst activity in cracking and deoxygenation reactions. The yield of biofuels could be increased from 37.32% to 40.00% by using the modified HY catalyst. Furthermore, the selectivity of gasoline could be achieved up to 11.79%. The Ni and Co metals impregnation on HY zeolite has a promising result on both the cracking and deoxygenation process of palm oil to biofuels due to the role of each metal. This finding is valuable for further catalyst development, especially on bifunctional catalyst development for palm oil conversion to biofuels.
High Acidity and Low Carbon-Coke Formation Affinity of Co-Ni/ZSM-5 Catalyst for Renewable Liquid Fuels Production through Simultaneous Cracking-Deoxygenation of Palm Oil Istadi Istadi; Teguh Riyanto; Didi Dwi Anggoro; Cokorda Satrya Pramana; Amalia Rizqi Ramadhani
Bulletin of Chemical Reaction Engineering & Catalysis 2023: BCREC Volume 18 Issue 2 Year 2023 (August 2023)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.17974

Abstract

This study investigates the effect of chemically doped Co and Ni metals on ZSM-5 catalyst with respect to the catalysts’ characteristics and performance for palm oil cracking. Some characterization methods have been conducted to identify the physicochemical properties of the synthesized catalysts, including X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), N2-physisorption, NH3- and CO2-probed Temperature Programmed Desorption (NH3-TPD and CO2-TPD) methods. The deposited carbon-coke on the spent catalysts is analysed using simultaneous thermal gravimetric – differential scanning calorimetry (TG-DTG-DSC) analysis. The performance of catalysts was evaluated on palm oil cracking process in a continuous fixed-bed catalytic reactor at 450 °C. To determine the liquid product composition functional group and components, we used Attenuated Total Reflectance Fourier-transform Infrared Spectroscopy (ATR-FTIR) and batch distillation methods, respectively. We found that the Co metal chemically-doped on Ni/SM-5 catalyst, resulting the increase in the catalysts acidity and the decrease in catalysts basicity. The conversion of palm oil increases as the increase of the ratio of catalysts’ acidity to basicity. The highest triglyceride conversion (76.5%) was obtained on the 3Co-Ni/ZSM-5 with the yield of gasoline, kerosene, and diesel of 2.61%, 4.38%, and 61.75%, respectively. It was also found that the chemically doping Co metal on Ni/ZSM-5 catalyst decreased carbon-coke formation due to the low catalysts’ basicity. Overall, it is proven that the combination of Co and Ni, which chemically doped, on ZSM-5 catalyst has a good activity in palm oil conversion with low carbon-coke formation affinity and high acidity of catalyst.