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Program Studi Kimia Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Udayana Kampus Bukit Jimbaran, Jimbaran, Bali, Indonesia
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Jurnal Kimia (Journal of Chemistry)
Published by Universitas Udayana
ISSN : 19079850     EISSN : 25992740     DOI : 10.24843/JCHEM
Core Subject : Science,
Chemistry
Jurnal Kimia (Journal of Chemistry) publishes papers on all aspects of fundamental and applied chemistry. The journal is naturally broad in scope, welcomes submissions from across a range of disciplines, and reports both theoretical and experimental studies.
Arjuna Subject : Kimia(semua kategori) - Kimia (Lain-Lain)
Articles 13 Documents
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Search results for , issue "Vol. 6, No. 1 Januari 2012" : 13 Documents clear
BIOSORPSI Cr(III) PADA BIOSORBEN SERAT SABUT KELAPA HIJAU TERAMOBILISASI EDTA I Wayan Sudiarta; Wahyu Dwijani Sulihingtyas
Jurnal Kimia (Journal of Chemistry) Vol. 6, No. 1 Januari 2012
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

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Abstract

Studies on biosorption of Cr(III) on coconut fiber immobilized with EDTA biosorbent (B-EDTA) have been conducted. These studies included the optimization of EDTA immobilization on biosorbent, optimization of Cr(III) biosorption on B-EDTA biosorbent that include pH dan contact time biosorption, and also studied the mechanisms of Cr(III) interactions on biosorbent B-EDTA by squential desorption.The result showed that the optimum EDTA immobilization on biosorbent E-EDTA occured at ratio of 1mmol EDTA : 4g biosorbet (0,25mmol/g ), with the surface acidity of biosorbent B-EDTA of 2,18 mmol/g. Optimum biosorption process of Cr(III) on biosorbent B-EDTA occured at pH = 3, contact time of 120 minutes, with the biosorption capacity of Cr(III) on biosorbent B-EDTA of 8,32 mg/g. The squential desorption studies show that the interaction of Cr(III) on biosorbent B-EDTA occured predominantly through physical adsorption namely Van der Waals bonding.
ISOLASI DAN IDENTIFIKASI SENYAWA GOLONGAN FLAVONOID DARI MADU K ELENGKENG (Nephelium longata L.) Ida Ayu Raka Astiti Asih; Ketut Ratnayani; Ida Bagus Swardana
Jurnal Kimia (Journal of Chemistry) Vol. 6, No. 1 Januari 2012
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

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Abstract

The determination of anti free radical activity on longan honey (Nephelium longata L.) by DPPH method using UV-Vis sphectrophotometry and identification of chemical compound in non polar and semi polar fraction have been done. Longan honey was diluted with methanol and then partied by n-hexane and ethyl acetate. The absorbance was measured at 497 nm, 517 nm, and 537 nm for the DPPH concentration of : 0,001%, 0,002%, 0,003%, and 0,004% and the chemical compound was identified by phytochemical method.The result showed that part of n-hexane and ethyl acetate probably consist of chemical compound of isoflavone and value of anti free radical activity on longan honey in semi polar fraction was higher than in non polar fraction which were 91,71% and 77,68% at DPPH concentration of 0,001% (b/v).
SINTESIS PESTISIDA FLUSILAZOL Aldes Lesbani; Hitoshi Kondo; Yoshinori Yamanoi; Hiroshi Nishihara
Jurnal Kimia (Journal of Chemistry) Vol. 6, No. 1 Januari 2012
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (244.901 KB)

Abstract

Flusilazole pesticide has been synthesized through coupling reaction of organosilica and aryl halide using palladium catalyst in basic condition under argon atmospherie in two reaction steps. The product was characterized using 1H and 13C NMR spectroscopy at 500 MHz and 125 MHz respectively.The results of this research showed that the high yield of colorless oil product was obtained up to 70%. 1H and 13C NMR spectra have six and eight peaks respectively, which indicate the structure of flusilazole.

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