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All Journal Journal of Tropical Life Science : International Journal of Theoretical, Experimental, and Applied Life Sciences JURNAL KIMIA SAINS DAN APLIKASI Teknotan: Jurnal Industri Teknologi Pertanian Jurnal Ilmu Kimia Universitas Brawijaya Bulletin of Chemical Reaction Engineering & Catalysis Journal of Innovation and Applied Technology Jurnal Pembangunan dan Alam Lestari Natural B The Journal of Pure and Applied Chemistry Research Jurnal Penelitian Pendidikan IPA (JPPIPA) Indonesian Journal of Chemistry Indonesian Food Science and TechnologyJournal Media Akuakultur Makara Journal of Science Bulletin of Chemical Reaction Engineering & Catalysis
Siti Mariyah Ulfa
Department Of Chemistry, Faculty Of Mathematics And Natural Sciences, Brawijaya University, Jl. Veteran, Malang 65145, Indonesia
Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Chemical Engineering, Chemistry & Bioengineering Chemistry Civil Engineering, Building, Construction & Architecture Computer Science & IT Control & Systems Engineering Decision Sciences, Operations Research & Management Education Engineering Environmental Science Materials Science & Nanotechnology Medicine & Pharmacology Physics Other

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Journal : Natural B

 1 
Ni / MgO Bifunctional Catalyst for Condensation and Furfural Hydrogenation Reactions in One Stage Produce Alkana C8-C13 Derived Compounds Siti Mariyah Ulfa; Indah Nur Pramesti
Natural B, Journal of Health and Environmental Sciences Vol 3, No 2 (2015)
Publisher : Natural B, Journal of Health and Environmental Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1589.242 KB) | DOI: 10.21776/ub.natural-b.2015.003.02.6

Abstract

Ni/MgO catalyst has been designed as bifunctional catalyst for condensation reaction of furfural and acetone followed by hydrogenation reaction to produce C8-C13 alkane derivatives in one step reaction. Ni/MgO catalyst was prepared by wet impregnation methods using Ni(NO3)2.6H2O and MgO as supporting material. The charcterization by X-ray diffraction (XRD) showed the characteristic of Ni on 2q = 44,27o; 51,59o and 75,89o. Isoterm adsorpsi using N2 gas gave the decreasing surface area of MgO and forming microporous structure. The activity test of the catalyst was carried out using furfural and acetone (1:1) in autoclave bath system, heated at 100-180oC for 7-8 hours in the presence of water. Ni/MgO catalyst showed the good activity when hydrogenation reaction performed at 150oC lead to the conversion of alkane derivatives in 95.69%. Characterization of the product by GC-MS showed the formation of 4-(2-furanyl)-2-butanone; 1,5-di(2-furanyl)-3-pentanone and 1,5-di(2-furanyl)-3-(1-pentenone) from reduction of C=C alkene of furfurylidene acetone. 
Activity Test Ni/ZrO2-SiO2 Catalyst for Hydrodeoxygenation Reactions Mixtures the Furfurylidene Acetone Compound (FAc) and Difurfurylidene Acetone (F2Ac) Dita Prihartini; Siti Mariyah Ulfa; Elvina Dhiaul Iftitah
Natural B, Journal of Health and Environmental Sciences Vol 3, No 3 (2016)
Publisher : Natural B, Journal of Health and Environmental Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (546.125 KB) | DOI: 10.21776/ub.natural-b.2016.003.03.08

Abstract

Hydrodeoxygenation (HDO) reaction of furfural derivatives have widely studied because these reaction produce saturated alkane which potensial for renewable fuels. Nickel based catalyst impregnated in to ZrO2-SiO2 (Ni/ZrO2-SiO2) was prepared and its activity is evaluated for HDO of furfurilidene aceto (FAc) and difurfurilidene acetone (F2Ac). Ni/ZrO2-SiO2 catalys was prepared from Ni(NO3)2.6H2O with 10% Ni loading over ZrO2-SiO2 by wet impregnation method. Characterization using X-ray showed the diffraction of Ni detected at 2θ = 44.42, 51.73, and 76.26. Catalyst activity for HDO of FAc and F2Ac was carried out at 200oC for 2 hours in batch system. According to gas chromatography analysis, the conversion of product is 100% with selectivity for 2-octanol and dodeka-6-ene is 88,22% and 2,99%, respectively.
Synthesis of 2-Methoxy-3H-Azepine Derived Compounds Through the Thermal Reaction between Alkylnitrobenzene and Tributylphosphine Siti Mariyah Ulfa; Hideki Okamoto; Kyosuke Satake
Natural B, Journal of Health and Environmental Sciences Vol 3, No 1 (2015)
Publisher : Natural B, Journal of Health and Environmental Sciences

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (531.661 KB) | DOI: 10.21776/ub.natural-b.2015.003.01.3

Abstract

Although photolysis of phenyazide has been widely reported to give 3H-azepine, the thermal deoxygenation reaction of alkylnitrobenzene derived similar products hitherto unexplored. Novel synthesis of 2-methoxy-3H-azepine derivatives was carried out using alkylnitrobenzene with tributylphosphine (Bu3P) reacted at 150°C for 24 hours in the presence of methanol. Reaction of m-nitrobenzene with the above methods gave two isomers of 3H-azepine, namely, 2-methoxy-6-methyl-3H-azepine and 2-methoxy-4-methyl-3H-azepine in 61%. Reaction of 2,3-dimethylnitrobenzene with Bu3P afforded the three isomers, that is, 2-methoxy-6,7-dimethyl-3H-azepine; 2-methoxy-3,4-dimethyl-3H-azepine and 7-methoxy-5,6-dimethyl-4H-azepine. Reaction of 3,5-dimethylnitrobenzene gave the sole product of 2-methoxy-4,6-dimethyl-3H-azepine in 42%. In contrast, reaction of 2,6-dimethylnitrobenzene didn’t give any product because the steric effect of methyl groups attached on C2 and C6. Structure elucidation of all novel products have confirmed by HETCOR. 
Co-Authors A.A. Ketut Agung Cahyawan W Adam Mahfud Ade Cintyia Sally Al zamzami, Ilham Misbakudin Alma Miranda Amaniyah, Amaniyah Amin, Abd Aziz Amini, Helda Wika Andi Kurniawan Andi Kurniawan Anggayasti, Wresti L. Anjani, Ryzki Martha Arda Rista Lestari Caterina Widya Astutik Chairulita Putri Kusumaningsih Dinia Rizqi Dwijayanti Dwi Susanti, Yogita Ayu Edi Priyo Utomo Edi Priyo Utomo Edi Priyo Utomo Efani, Anton Eka Novitasari Elvina Dhiaul Iftitah Elvina Dhiaul Iftitah Elvina Dhiaul Iftitah Esya, Firdausy Amalina Fadlilah, Lilik Nur Fath Dwisari Fatma, Aliya Galisong, Ridwan Danuarta Grahadi, Rahmat Gunawan, Firza Rajasa Hapsari, Febriyana Rizky Helda Wika Amini Hermanto, Feri Eko Hidayatul Mustafidah Hideki Okamoto Hideki Okamoto Iftitah, Elvina Dhiaul Indah Nur Pramesti Inra Sari Kamila, Fairuz Sarah Karimah Karimah Kyosuke Satake Kyosuke Satake Lisa Aulia, Lisa Listianingsih, Lia Lukman Hakim Lukman Hakim Lutfi Ni’matus Salamah Luthfia Ayu Dhea Maharani Pertiwi Koentjoro Mahfuzh Huda Masruri Masruri Masruri Masruri Masruri Moehammad, Khibar Syiar Moh. Farid Rahman Mohammad Elham Firdaus Mohammad Farid Rahman Mohammad Farid Rahman Momodou Salieu Sowe Momodou Salieu Sowe Nashi Widodo Nisa', Khibrun Nur Ikhtiarini Nuraini Uswatun Chasana Pangesti, Laras Pramudia, Zulkisam Pratama, Safreno Panggih Pratiwi, Rahmania Tulus Setya Prihartini, Dita Puspitasari, Rizka Dwitya Rachmat Triandi Tjahjanto Rizka Fauzia Ohorella Rizqi Alima Fabri, Ahmad Rosyadah, Nuraini Safitri, Anna Salamah, Lutfi Ni’matus Suratmo, Suratmo SUTRISNO Sutrisno, Sutrisno Utomo, Edi Priyo Wardani, Eris Agustin Warsito Warsito Warsito Warsito Widia Edy Kuncoro Widodo Widodo Widyananda, Muhammad Hermawan Yanuar, Adi Tiya Yosua Yosua Yulistian, Dhoni Prielananta Yusnawan, Eriyanto Yusuf Hendrawan Zahara, Izaz Aqeiluz