Wega Trisunaryanti
Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Sekip Utara, Yogyakarta 55281, Indonesia

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Hydrocracking of α-Cellulose Using Co, Ni, and Pd Supported on Mordenite Catalysts Wega Trisunaryanti; Triyono Triyono; Ria Armunanto; Lathifah Puji Hastuti; Desinta Dwi Ristiana; Resi Vita Ginting
Indonesian Journal of Chemistry Vol 18, No 1 (2018)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (463.335 KB) | DOI: 10.22146/ijc.26491

Abstract

Hydrocracking of α-cellulose has been conducted in a semi-batch reactor at 400, 450, and 500 °C with hydrogen flow (30 mL/min.) for 4 h. Mordenite (MOR) and Co, Ni and Pd metal supported on the MOR were used as solid catalysts. The catalysts were characterized using X-ray Diffractometer (XRD), Fourier Transform Infrared (FTIR) spectroscopy, and Scanning Electron Microscopy (SEM) to evaluate the physical-chemical properties. Energy Dispersive X-ray (EDX) and Inductively Coupled Plasma (ICP) were used to analyze the amount of metal impregnated on the catalysts. The liquid product was analyzed using Gas Chromatograph-Mass Spectroscopy (GC-MS). Thermal hydrocracking was also conducted at 450 °C with the amount of liquid product was 37.86 wt.%. The highest liquid conversion obtained by mordenite catalyst was 94.66 wt.% at 450 °C and the highest liquid conversion (98.08 wt.%) was reached by Pd/MOR catalyst at 400 °C.
Transesterification of Used Cooking Oil Using CaO/MCM-41 Catalyst Synthesized from Lapindo Mud by Sonochemical Method Ida Bagus Putra Mahardika; Wega Trisunaryanti; Triyono Triyono; Dwi Putra Wijaya; Kumala Dewi
Indonesian Journal of Chemistry Vol 17, No 3 (2017)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (14.303 KB) | DOI: 10.22146/ijc.26561

Abstract

Transesterification of waste cooking oil using CaO/MCM-41 synthesized from Lapindo mud by the sonochemical method has been carried out. The silica was separated from the mud by reflux method used 6 M HCl and 6 M NaOH. The silica was then analyzed by XRF and used as silica source in MCM-41 synthesis. The synthesis of MCM-41 was carried out by the sonochemical method, then analyzed by XRD, Infrared spectrophotometer, SAA, and TEM. The Ca2+ was loaded onto the MCM-41 by wet impregnation method under variation of the Ca2+ content of 1.15, 1.29, 2.39, and 3.25 wt.% analyzed by ICP produced CaO(1), CaO(2), CaO(3), and CaO(4)/MCM-41 catalyst respectively. Transesterification of used cooking oil was carried out under methanol/oil mole ratio of 15/1, the temperature of 55, 65 and 75 °C, and catalyst/oil weight ratio of 5/100, 10/100 and 15/100 for 2 h by reflux method. The XRD analysis of the MCM-41 showed a characteristic peak at 2θ = 2-5°. The MCM-41 has a specific surface area of 1290 m2/g and pore diameter of 3.4 nm. The TEM images of MCM-41 showed ordered pore distribution with a hexagonal shape. The highest conversion of methyl ester was 78.17 wt.% obtained under the reaction conditions at 65 °C and catalyst/oil weight ratio of 15/100 using the CaO(4)/MCM-41. The lifetime CaO(4)/MCM-41 catalyst was 9.8 h.
Synthesis of Ce-Mesoporous Silica Catalyst and Its Lifetime Determination for the Hydrocracking of Waste Lubricant Wega Trisunaryanti; Triyono Triyono; Iip Izul Falah; Andreas David Siagian; Muhammad Fajar Marsuki
Indonesian Journal of Chemistry Vol 18, No 3 (2018)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (382.43 KB) | DOI: 10.22146/ijc.31717

Abstract

The synthesis of Ce/mesoporous silica (Ce/MS) and its lifetime determination for the hydrocracking of waste lubricant has been carried out. The MS was synthesized using tetraethyl orthosilicate (TEOS) and gelatin extracted from bovine bone as a template. Cerium was impregnated onto the MS by wet impregnation method using Ce(NO3)3.6H2O. The MS and Ce/MS were then characterized by means of acidity using ammonia base vapor adsorption, Fourier Transform Spectrophotometer (FTIR), Transmission Electron Microscope (TEM), Scanning Electron Microscope-Energy Dispersive X-ray Spectrometer (SEM-EDX), and surface area analyzer (SAA) based on the BET and BJH equation. The Ce/MS catalyst was tested in hydrocracking of waste lubricant in three runs. Lifetime of Ce/MS catalyst was determined using a linear regression of the liquid product yields vs hydrocracking time. The Ce/MS catalyst showed an acidity of 2.79 mmol/g, BJH desorption pore diameter of 3.84 nm, BET surface area of 246.55 m2/g, and total pore volume of 0.44 cm3/g. The yield of liquid product obtained from hydrocracking of waste lubricant using the Ce/MS catalyst for the first, second, and third runs was 21.42, 17.23 and 10.54 wt.%, respectively for 2.5 h per each run. Lifetime of Ce/MS catalyst in hydrocracking of waste lubricant was 12.54 h.
Synthesis of Mesoporous Carbon from Merbau Wood (Intsia spp.) by Microwave Method as Ni Catalyst Support for α-Cellulose Hydrocracking Andaru Dena Prasiwi; Wega Trisunaryanti; Triyono Triyono; Iip Izul Falah; Darma Santi; Muhammad Fajar Marsuki
Indonesian Journal of Chemistry Vol 19, No 3 (2019)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (373.546 KB) | DOI: 10.22146/ijc.34189

Abstract

Synthesis of mesoporous carbon from Merbau wood (Intsia spp.) waste by microwave method as nickel catalyst support for α-cellulose hydrocracking had been carried out. The Merbau wood sawdust was carbonized at 800 °C to produce C800 and the C800 was treated by microwave irradiation (399 W) for 5 min to produce C800MW. The Merbau wood flakes, which were only treated by microwave irradiation (399 Watts) for 30 min produced CMW. Wet impregnation technique was carried out to disperse the Ni metal (1.0, 1.5, and 2.0 wt.%) onto the best mesoporous carbon. The mesoporous carbons were analyzed by Fourier Transform Infra-Red Spectroscopy (FTIR), Surface Area Analyzer (SAA) and Scanning Electron Microscopy (SEM). The hydrocracking of pyrolyzed α-cellulose was carried out at 400 °C. The liquid product was analyzed by Gas Chromatograph-Mass Spectrometer (GC-MS). The results showed that the C800MW was the best performance carbon and it had a specific surface area, total pore volume, average pore diameter and acidity of 364.12 m2/g, 0.28 cm3/g, 3.03 nm, and 2.18 mmol/g, respectively. The Ni1.5/C800MW catalyst produced the highest conversion of liquid product (58.76 wt.%) than the Ni1/C800MW (57.51 wt.%) and Ni2/C800MW (34.18 wt.%).
Synthesis of Iron-Doped Zirconium Titanate as a Potential Visible-Light Responsive Photocatalyst Rian Kurniawan; Sri Sudiono; Wega Trisunaryanti; Akhmad Syoufian
Indonesian Journal of Chemistry Vol 19, No 2 (2019)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (243.375 KB) | DOI: 10.22146/ijc.38616

Abstract

Synthesis and properties of iron-doped zirconium titanate (ZrTiO4) as a potential visible-light-responsive photocatalyst had been conducted. Various iron dopant concentration and calcination temperature were investigated toward the properties of Fe-doped ZrTiO4. The photocatalyst material was synthesized by sol-gel and impregnation method. Titanium tetraisopropoxide (TTIP) was used as a precursor, embedded on zirconia fine powder. A certain amount of iron (1, 3, 5, 7 and 9 wt.%) was introduced into the photocatalyst system from iron(II) sulfate heptahydrate (FeSO4·7H2O). Photocatalyst with various iron concentration calcined at 500 °C. ZrTiO4 with 5% iron additionally was calcined at 700 and 900 °C. Characterization was performed by using XRD, FT-IR, SR-UV, and SEM-EDX. The presence of iron on the surface of ZrTiO4 was proved by EDX analysis. Fe-doped ZrTiO4 with the lowest bandgap (2.83 eV) is 7% of iron content after calcination at 500 °C.
Coating of Pd and Co on Mordenite for a Catalyst of Hydrotreating of Cashew Nut Shell Liquid into Biofuel Maya Tri Hapsari; Wega Trisunaryanti; Iip Izul Falah; Media Laila Permata
Indonesian Journal of Chemistry Vol 20, No 5 (2020)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (414.344 KB) | DOI: 10.22146/ijc.48633

Abstract

The catalytic activity of Co and Pd loaded on mordenite (MOR) was evaluated in the hydrotreatment of cashew nut shell liquid (CNSL) into biofuel. Metals were loaded into MOR as support via wet impregnation process. The Co content was varied as 2, 4, and 6 wt.% to produce Co(1)/MOR, Co(2)/MOR, Co(3)/MOR catalysts. The micro-mesoporous structure of the catalyst was confirmed by XRD, SEM, TEM, FTIR, and N2 adsorption-desorption measurement. AAS were used to analyze the amount of metal that is successfully loaded in the catalysts. Hydrotreating of the CNSL was conducted in a semi-batch reactor at 450 °C with hydrogen flow (20 mL/min) for 2 h. The liquid product was analyzed using GC-MS. The activity of Co/MOR was compared with the activity of Pd/MOR as a noble metal. The result of the hydrotreatment process showed a decrease of liquid product in the sequence of Co(3)/MOR > Co(2)/MOR > Pd/MOR > Co(1)/MOR > MOR. The Co(3)/MOR catalyst exhibited the highest conversion of liquid hydrocarbon than the others (61.8 wt.%), comprising predominantly by gasoline compounds with over 25.21 wt.% conversion.
Cobalt Doping on Zirconium Titanate as a Potential Photocatalyst with Visible-Light-Response Emilya Faridatul Sulaikhah; Rian Kurniawan; Mokhammad Fajar Pradipta; Wega Trisunaryanti; Akhmad Syoufian
Indonesian Journal of Chemistry Vol 20, No 4 (2020)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (14.694 KB) | DOI: 10.22146/ijc.49459

Abstract

Synthesis of cobalt-doped zirconium titanate (Co-doped ZrTiO4) as a potential photocatalyst with visible-light-response had been conducted. Materials used in this research were titanium tetraisopropoxide (TTIP) as a precursor of TiO2, ZrO2 as another semiconductor for coupling, and CoSO4·7H2O as the source of cobalt dopant. The composite was prepared by the sol-gel method with various cobalt contents and calcination temperatures. Composites with various Co dopant contents (0, 1, 3, 5, 7, and 9% (Co wt./Ti wt.)) were calcined at 500 °C for 4 h. In addition, the composite with 5% of dopant content was calcined at 700 and 900 °C to observe the influence of calcination temperature. All samples were characterized by using X-ray powder diffraction method (XRD), Fourier-transform infrared spectroscopy (FTIR), specular reflectance UV-Vis spectroscopy (SRUV), and scanning electron microscopy equipped with X-ray energy dispersive spectroscopy (SEM-EDS). Co-doped ZrTiO4 with the lowest bandgap (2.94 eV) was achieved in a sample containing 3% of cobalt content calcined at 500 °C.
Hydrotreatment of Cellulose-Derived Bio-Oil Using Copper and/or Zinc Catalysts Supported on Mesoporous Silica-Alumina Synthesized from Lapindo Mud and Catfish Bone Fahri Swasdika; Wega Trisunaryanti; Iip Izul Falah
Indonesian Journal of Chemistry Vol 21, No 2 (2021)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.50558

Abstract

Catalysts comprising copper and/or zinc supported on mesoporous silica-alumina (MSA) with a high Si/Al ratio were prepared by wet impregnation method. This study investigated the preparation, characterization, and catalytic application of the prepared catalysts for hydrotreatment cellulose-derived bio-oil. The wet impregnation was performed by directly dispersing Cu(NO3)2·3H2O and/or Zn(NO3)2·4H2O aqueous solution into MSA, followed by calcination and reduction under H2 gas stream. The acidity test revealed that metal addition on MSA support increases the acidity of catalysts. During hydrotreatment of cellulose-derived bio-oil CuZn/MSA with total acidity, copper loading, zinc loading, and specific surface area of 24.86 mmol g–1, 5.23 wt.%, 3.15 wt.%, and 170.77 m2 g–1, respectively, exhibited the best performance compared to other prepared catalysts with 90.49 wt.% conversion of liquid product.
Acid-Alkaline Treatment of Mordenite and Its Catalytic Activity in the Hydrotreatment of Bio-Oil Febi Yusniyanti; Wega Trisunaryanti; Triyono Triyono
Indonesian Journal of Chemistry Vol 21, No 1 (2021)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.51496

Abstract

Acid-alkaline treatment using acetic acid and sodium hydroxide (NaOH) were applied on mordenite (MOR) to increase the Si/Al ratio and surface area properties. Various time treatment (3, 6, and 9 h) and concentration of acetic acid (6, 9, and 12 M) were used to treat MOR, and followed by the treatment with NaOH (0.1 M) under room temperature. The MOR and treated mordenite were applied as a catalyst for hydrotreatment of cellulose-derived bio-oil. The acetic acid treatment caused the increase of the Si/Al ratio of mordenite up to 27.03. The Si/Al ratio was determined using ICP-AES analysis which was also confirmed using FT-IR analysis. The acidity was determined using NH3 vapors adsorption. The acidity test revealed that as the Si/Al ratio increased the acidity of mordenite decreased. The advantage of using acetic acid for acid treatment was that the XRD patterns of mordenite can be preserved with a little decrease of the intensity. On the other hand, the NaOH treatment under room temperature decreased the crystallinity down to 68%, which was calculated using XRD. The acid-alkaline treatment of mordenite succeeded to increase the surface area 2 times larger than the parent mordenite. The surface area was obtained from BET analysis. The acid-alkaline treated mordenite exhibited better catalytic activity upon hydrotreatment of biomass-derived bio-oil compared to the parent mordenite which corresponded to its highest surface area.
Enhancement of Cobalt Concentration Supported on Mesoporous Silica towards the Characteristics and Activities of Catalysts for the Conversion of Waste Coconut Oil into Gasoline and Diesel Oil Wega Trisunaryanti; Triyono Triyono; Nugroho Raka Santoso; Savitri Larasati; Cahyarani Paramesti; Dyah Ayu Fatmawati
Indonesian Journal of Chemistry Vol 21, No 3 (2021)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.22146/ijc.55633

Abstract

The analysis of the effect of cobalt concentration supported on mesoporous silica (MS) has been evaluated. This study was aimed to observe the physical and chemical characteristics of the catalysts, and also to study the catalytic activity and its selectivity towards gasoline and diesel oil products in the hydrocracking process of waste coconut oil. The MS was produced using Lapindo mud, where the CTAB was used as the mesopore templating agent. The Co/MS catalyst was prepared by the wet impregnation method with various concentrations of Co. The characterization of the catalyst includes silica purity test by XRF, determination of Co content by AAS, the crystallinity by XRD, the catalyst porosity by SAA, physical pore structure by SEM and TEM, and total acidity by the gravimetric method using NH3 base vapor adsorption. The hydrocracking was carried out in a hydrocracking reactor using various concentrations of Co/MS catalysts with the ratio of catalyst/feed = 1/50. The products of the hydrocracking process were liquid, coke, and gas. The composition of the hydrocracking liquid products was analyzed by GC-MS. Based on the results of the catalytic activity test, it was concluded that the Co(1)/MS catalyst, which had the highest acidity, showed the best catalyst selectivity towards gasoline and diesel fractions.