Anis Kristiani, Anis
Research Center for Chemistry, Indonesian Institute of Science, Kawasan Puspiptek Serpong, Tangerang Selatan 15314, Banten

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Performance of sulfided NiMo catalyst supported on pillared bentonite Al and Ti under hydrodeoxygenation reaction of guaiacol Rinaldi, Nino; Sari, Novi Liana; Sumari, S.; Kristiani, Anis; Agustian, Egi; Widjaya, Robert Ronald; Dwiatmoko, Adep
International Journal of Renewable Energy Development Vol 13, No 3 (2024): May 2024
Publisher : Center of Biomass & Renewable Energy (CBIORE)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.61435/ijred.2024.60060

Abstract

Bio-crude oil is known to be sustainable, eco-environmentally, and an alternative energy source produced by biomass pyrolysis. However, its quality remains relatively low due to a higher oxygen concentration compared to liquid fuels from fossils. Therefore, an upgrading process is necessary through the catalytic hydrodeoxygenation (HDO) process. This work synthesized pillared bentonite using Al and Ti metals as the pillaring agent to produce Al-PILC and Ti-PILC as catalyst support for sulfided NiMo. Their catalytic activity in HDO reaction using guaiacol as a model compound of bio-crude oil were also evaluated. Characterization of the bentonite-pillared materials, including Al-PILC, Mo/Al-PILC, NiMo/Al-PILC, Ti-PILC, Mo/Ti-PILC, and NiMo/Ti-PILC, was performed using Surface Area Analyzer, X-ray Diffractometer (XRD), Temperature-Programmed Desorption of ammonia (NH3-TPD), X-Ray Fluorescence (XRF), and Scanning Electron Microscope (SEM) techniques. The characterization results confirm the pillarization process of bentonite using Al and Ti metals as the pillaring agent, and the preparation of the NiMo catalyst using the stepwise impregnation method was successfully prepared. The NiMo/Ti-PILC catalyst performs a superior conversion value on the HDO guaiacol reaction than other catalysts. A well dispersion of Mo and Ni metals on the surface support (NiMo/Ti-PILC), thus creating numerous active sites of the catalyst after the sulfidation. Variations in time and temperature during the HDO guaiacol reaction significantly affected the conversion.
Bimetallic Ni-Fe Supported by Gadolinium Doped Ceria (GDC) Catalyst for CO2 Methanation Kristiani, Anis; Takeishi, Kaoru; Jenie, Siti Nurul Aisyiyah; Petrus, Himawan Tri Bayu Murti
Bulletin of Chemical Reaction Engineering & Catalysis 2024: BCREC Volume 19 Issue 1 Year 2024 (April 2024)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20108

Abstract

CO2 conversion into fuels and high value-added chemical feedstocks, such as methane, has gained novel interest as a crucial process for further manufacturing multi-carbon products. Methane, CH4, becomes a promising alternative for environmental and energy supply issues. Nickel-based catalysts were found to be very active and selective for CH4 production. The use of promoter and support material to develop high activity, high selectivity, and durable catalysts for CO2 methanation at low temperature is a challenge. Gadolinium-Doped Ceria (GDC) has been known as material for Solid Oxide Fuel Cell (SOFC) and Solid Oxide Electrolysis Cell (SOEC) due to higher ionic conductivity and lower operating temperatures. However, few researches have been done regarding to CO2 methanation over GDC as catalyst support so far. In this present work, CO2 methanation was investigated over bimetallic Ni-Fe catalyst supported by GDC. The results showed that CH4 production rate by using Ni-Fe/GDC catalyst was higher than that of GDC at all reaction temperatures carried on. Ni-Fe/GDC showed remarkable CH4 production rate as of 17.73 mmol.gcat−1.h−1 at 280 °C. No catalytic activity was produced by GDC catalyst only. The highest CO2 conversion (46.50%) was observed at 280 °C, with almost 100% selectivity to CH4. The turnover frequency (TOF) value of Ni-Fe/GDC (4529.32 h−1) was the highest than that of Ni and common CO2 methanation catalyst, Ni/Al2O3 catalysts at 280 °C, further displaying the outstanding low-temperature catalytic activity. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
Tar Removal of Palm Kernel Shell Syngas using Wet Scrubber Putro, Firman Asto; Pranolo, Sunu Herwi; Waluyo, Joko; Basworo, Agung Tri; Norman, Hafiz; Kristiani, Anis; Hidayati, Luthfiana Nurul
Jurnal Rekayasa Kimia & Lingkungan Vol 19, No 1 (2024): Jurnal Rekayasa Kimia & Lingkungan (June 2024 )
Publisher : Chemical Engineering Department, Syiah Kuala University, Banda Aceh, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.23955/rkl.v19i1.33341

Abstract

In the current situation, biomass gasification has become a major interest in producing clean energy and green chemicals. By gasification, the biomass can be converted to synthetic gas (syngas) for many purposes. However, syngas with high tar content can cause pipeline fouling and disturb the operation of downstream equipment. To reduce tar content, a two-series wet scrubber was installed for syngas cleaning produced by palm kernel shell gasification. Firstly, the gasification is operated at a temperature range of 500 600oC and 700 800oC to determine the conditions where the lowest tar syngas is produced. After that, the wet scrubber is installed with a variety of solvents including isopropyl alcohol, water, used cooking oil, and used lubricating oil. The results show that the lowest tar syngas was produced at a temperature of 800oC with a tar yield of 0.165 g/kg biomass. Meanwhile, in the same condition, isopropyl alcohol delivers the most substantial impact on tar removal efficiency, whereas used lubricating oil results in less impact. The use of isopropyl alcohol resulted in 99.25% tar removal effectiveness while lubricating oil yielded just 50.32%.