UNIVERSITAS AIRLANGGA



Detail Article

Kimia FST

ISSN -

Vol. 1 / No. 1 / Published : 2013-07

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Original Article :

Pembuatan dan karakterisasi katalis asam fosfomolibdat terimpregnasi pada bentonit untuk transformasi anetol

Author :

  1. Dr. Alfinda Novi Kristanti, DEA*1
  2. Alfa Akustia Widati*2
  3. A’yunil Hisbiyah*3
  1. Dosen Departemen Kimia FST Unair
  2. Dosen Departemen Kimia FST Unair
  3. Mahasiswa

Abstract :

Anetol is the anise oil main content and can be transformed into their derivatives with a higher level of benefits. The objective of this research are use and to find out the catalytic activity of impregnated phosphomolybdic acid on bentonite (H3PMo12O40/bentonite) in anethole transformation. This research was started by making H3PMo12O40 catalyst which was impregnated into activated bentonite. Furthermore, H3PMo12O40/bentonite was characterized by XRD and FT-IR. Then, H3PMo12O40/bentonite was applied in anethole transformation at 60oC with reaction time variation were 1,2,3,4,5, and 6 hours. Reaction products were analyzed by TLC, UV-Vis spectrophotometer, and GC-MS. The XRD characterization results showed typical peak of H3PMo12O40 at 26o with a very high intensity. Acidity test analysis showed the Bronsted acid site moles number of 0.3340 mmol/g, while the Lewis acid site moles number of 7.45 x 10-3 mmol/g. From the results test of TLC and UV-Vis spectrophotometer, the H3PMo12O40/bentonit catalytic activity began to look at anethole transformation since the first one hour, the optimum reaction time of 3 hours with %anethole conversion of 61.54%, and was obtained anethole’s λmaks at 258.5 nm and product’s λmaks of 207 nm. From the analysis by GC-MS, was obtained the product molekol weight of 208 g/mole and 210 g/mole.

Keyword :

Anethole, Transformation, phosphomolybdic acid/bentonite,


References :

Bokade, V.V. and Yadav,(2007) Synthesis of Pharmaceutical Intermediates by Toluene Benzylation over Heteropoly Acids on Different Support swis : Journal of Natural Gas Chemistry





Archive Article

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Volume : 1 / No. : 1 / Pub. : 2013-07
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