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Studi Penggunaan Katalis Tembaga Molybdenum Oksida Berpenyangga Silica (CuMoO3/SiO2) Untuk Oksidasi Metana Menjadi Methanol Dan Formaldehida H. Husin; Marwan Marwan
Reaktor Volume 08 No.1 Juni 2004
Publisher : Dept. of Chemical Engineering, Diponegoro University

Studi penggunaan katalis tembaga molybdenum oksida berpenyangga silica (CuMoO3/SiO2) untuk oksidasi parsial metana menjadi methanol dan formaldehida telah dilakukan. Preparasi katalis dilakukan dengan metode impregnasi. Hasil identifikasi dengan XRD menunjukkan bahwa komponen katalis terdiri dari senyawa MoO3, Cu2Odan SiO2. Uji kinerja katalis dilangsungkan dalam reaktor pipa lurus berunggun tetap, beroperasi pada temperature 400, 450 dan 500 0C dan tekanan 1 atm. Produk reaksi dianalisis menggunakan gas kromatografi buatan Shimadzu dengan kolom mole sieve 5A dan porapak Q. Konversi metana tertinggi diperoleh 34,1% menggunakan katalis dengan rasio Cu: Mo 1: 3, temperatur reaksi 400 0C. Perolehan methanol tertinggi 3,4 % dan perolehan formaldehida tertinggi 7,3%.Kata kunci : oksidasi parsial metana, katalis (CuMoO3/SiO2), impregnasi, methanol, formaldehida

Production of Triacetin by Microwave Assisted Esterification of Glycerol Using Activated Natural Zeolite Marwan Marwan; Eti Indarti; Darmadi Darmadi; Wahyu Rinaldi; Dzikri Hamzah; Taufik Rinaldi
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 3 Year 2019 (December 2019)
Publisher : Department of Chemical Engineering - Diponegoro University

Triacetin, an alternative biodiesel additive, was prepared by esterification of glycerol with acetic acid in the presence of chemically activated natural zeolite. The esterification was carried out in a small reaction flask under microwave irradiation. The catalyst was characterized for its morphology by SEM and its chemical composition by X-ray Diffraction (XRD). The Scanning Electron Microscopy (SEM) micrograph indicates improved surface area of the zeolite, while the XRD analysis shows an increase in Si/Al ratio from natural zeolite to 6.042 and its crystallinity value of 12.23%. The Fourier Transform Infra Red (FTIR) analysis obtained showed that microwave-heated samples have an esters group spectrum of triacetin at 1702 cm-1. The conversion value of glycerol was more than 95% at molar ratio of the reactants 1:9 and catalyst loading of 3%. The selectivities for monoacetin, diacetin and triacetin were 80.1%, 15.4%, and 4.5% at 60 minutes, and 43.0%, 48.6%, and 8.3% at 90 minutes. It shows that the conversion took place in consecutive steps and the use of microwave allows the reaction proceeding at milder condition.

Characterization of Titania (TiO2) Catalysts Prepared by Sol-Gel Method Marwan Marwan; Naoto Azuma; Akinori Maezawa; Shigeo Uchida
ASEAN Journal of Chemical Engineering Vol 3, No 1 (2003)
Publisher : Department of Chemical Engineering, Universitas Gadjah Mada

Various TiO2 catalysts in powder form were prepared ny sol-gel method and then characterized for X-ray diffraction and BET surface area. VAriation in composistion of reactants, choice of hydrolysing catalyst, calcination temperature, and method of drying were among preparative variable evaluated. Addition Pt, Fe2O3, CuO and SiO2 on the catalysts was also carried out during the initial stage of sol formation. XRD analysis suggest that all catalysts calcined at 450'C were compeltelu in anatase phase. BET surface area of the catalysts revealed that the catalysts prepared using HNO3 as hydrolysing catalyst, have a surface area larger than the commercial Degussa P25 TiO2 catalyst, with the highest area of 126m2/g. The addition of metals resulted in a lower surface area, while silica provided a considerable incdease in surface area, at 257 m2/g. Analyses of isotherms plot and BJH desorption plots suggest that particle pores were dominated by a bottle-like share. However, the photocalatylstic activity of these catalysts in te degradation of sufactant failed to meet the perfomance rating of Degussa P23 TiO2 catalyst, probably due to less access of surfactant into interbal surface of the prepared catalysts. Degradation of the surfactant usidng different particle sizes suggests that the external surface of TiO2 catalysts was important under liquid phase degradation.

Production of Triacetin by Microwave Assisted Esterification of Glycerol Using Activated Natural Zeolite Marwan Marwan; Eti Indarti; Darmadi Darmadi; Wahyu Rinaldi; Dzikri Hamzah; Taufik Rinaldi
Bulletin of Chemical Reaction Engineering & Catalysis 2019: BCREC Volume 14 Issue 3 Year 2019 (December 2019)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.14.3.4250.672-677

Triacetin, an alternative biodiesel additive, was prepared by esterification of glycerol with acetic acid in the presence of chemically activated natural zeolite. The esterification was carried out in a small reaction flask under microwave irradiation. The catalyst was characterized for its morphology by SEM and its chemical composition by X-ray Diffraction (XRD). The Scanning Electron Microscopy (SEM) micrograph indicates improved surface area of the zeolite, while the XRD analysis shows an increase in Si/Al ratio from natural zeolite to 6.042 and its crystallinity value of 12.23%. The Fourier Transform Infra Red (FTIR) analysis obtained showed that microwave-heated samples have an esters group spectrum of triacetin at 1702 cm-1. The conversion value of glycerol was more than 95% at molar ratio of the reactants 1:9 and catalyst loading of 3%. The selectivities for monoacetin, diacetin and triacetin were 80.1%, 15.4%, and 4.5% at 60 minutes, and 43.0%, 48.6%, and 8.3% at 90 minutes. It shows that the conversion took place in consecutive steps and the use of microwave allows the reaction proceeding at milder condition.

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