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Indonesian Journal of Chemistry

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Published by Universitas Gadjah Mada

ISSN : 14119420 EISSN : 24601578 DOI : -

Core Subject : Science, Engineering,

Chemical Engineering, Chemistry & Bioengineering Chemistry

Indonesian Journal of Chemistry is an International, peer-reviewed, open access journal that publishes original research articles, review articles, as well as short communication in all areas of chemistry including applied chemistry. The journal is accredited by The Ministry of Research, Technology and Higher Education (RISTEKDIKTI) No : 21/E/KPT/2018 (in First Rank) and indexed in Scopus since 2012. Since 2018 (Volume 18), Indonesian Journal of Chemistry publish four issues (numbers) annually (February, May, August and November).

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Articles 31 Documents

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Search results for , issue "Vol 9, No 2 (2009)" : 31 Documents clear

TRANSFORMATION OF RICINOLEIC OF CASTOR OIL INTO LINOLEIC (OMEGA-6) AND CONJUGATED LINOLEIC ACID BY DEHYDRATION Marham Sitorus; S. Ibrahim; H. Nurdin; D. Darwis
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

The ricinoleic of Castor Oil was dehydrated by various dehydrator agent (P2O5, K2CO3, H3PO4, NaHSO4, Al2O3, molecular sieve and activated bentonite at 450 °C - HCl) on the same condition (150 °C, mol ratio 1:1 and 2 hours ). The compositions of Refined Ricinus Castor Oil as starting material were : 0.92% palmitic , 5.56% linoleic , 4.07% octadecanoic , 1.22% stearic and 85.06% ricinoleic. The spesific wave number of IR was bandwith 3411 cm-1 caused of hydroxyl (-OH) group of ricinoleic at C-12 as main component. The product was Dehydrated Castor Oil (DCO) mixed of linoleic (omega 6) [C18 : 2 (9,12)] and Conjugated Linoleic Acid (CLA) [C18: 2 (9,11)]. The best dehydrator was P2O5 based on three parameters were : Free Fatty Acid (FFA) nearly the same (1.855% of Castor oil and 2.139% of DCO), the most increased of Iodium value (49.860 mg/g of Castor oil in to 63.090 mg/g of DCO), and the most decresed of hydroxyl number (28.27 mg of Castor oil in to 17.75 mg/g of DCO). To optimized the dehydration was done by various number of P2O5 (3g, 5g and 7g), tempereture (room, 100 °C and 150 °C) and time (2h, 2.5h, 3h, and 3.5h). The optimal conditon of dehydration was not found yet. Some of sugestted or idea for dehydration were: dehydration must be done by base or netral, non oxydator dehydrator, mol ratio 1:1, temperature (100-150 °C) and 2-3.5 h. Based on GC-MS the best DCO (7g P2O5, 150 °C and 3.5 h) were showed that the decrease of ricinoleic 14.13% (85.08% of Castor Oil in to 70.93% of DCO), increased linoleic 2.09% (5.56 of Castor oil in to 7.65% of DCO) and conducted of 9.09% CLA. Some new peaks between linoleic and ricinoleic are maybe isomer's of linoleic and CLA. The wave number of cunjugated alkene (C=C) (1666.3 cm-1) of IR spectra of DCO together with GC-MS chromatogram's to indicated that linoleic and CLA were conducted.

AMINO AND MERCAPTO-SILICA HYBRID FOR Cd(II) ADSORPTION IN AQUEOUS SOLUTION Buhani Buhani; Narsito Narsito; Nuryono Nuryono; Eko Sri Kunarti
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

Modification of silica gel with 3-aminopropyltrimethoxysilane and 3-mercaptopropyltrimethoxysilane through sol-gel technique producing amino-silica hybrid (HAS) and mercapto-silica hybrid (HMS), respectively, has been carried out using tetraethylorthosilicate (TEOS) as silica source. The adsorbents were characterized using infrared spectroscopy (IR), and X-ray energy dispersion spectroscopy (EDX). Adsorption of Cd(II) individually as well as its binary mixture with Ni(II), Cu(II), and Zn(II) in solution was performed in a batch system. Adsorption capacities of Cd(II) ion on adsorbent of silica gel (SG), HAS, and HMS are 86.7, 256.4 and 319.5 μmol/g with the adsorption energies are 24.60, 22.61 and 23.15 kJ/mol, respectively. Selectivity coefficient (α) of Cd(II) ion toward combination of Cd(II)/Ni(II), Cd(II)/Cu(II), and Cd(II)/Zn(II) ions on HAS adsorbent is relatively smaller than those on HMS adsorbent which has α > 1.

ESTIMATION OF MEASUREMENT UNCERTAINTY IN THE DETERMINATION OF Fe CONTENT IN POWDERED TONIC FOOD DRINK USING GRAPHITE FURNACE ATOMIC ABSORPTION SPECTROMETRY Harry Budiman; Fransiska Sri H; Krismastuti Krismastuti; Nuryatini Nuryatini
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

The evaluation of uncertainty measurement in the determination of Fe content in powdered tonic food drink using graphite furnace atomic absorption spectrometry was carried out. The specification of measurand, source of uncertainty, standard uncertainty, combined uncertainty and expanded uncertainty from this measurement were evaluated and accounted. The measurement result showed that the Fe content in powdered tonic food drink sample was 569.32 µg/5g, with the expanded uncertainty measurement ± 178.20 µg/5g (coverage factor, k = 2, at confidende level 95%). The calibration curve gave the major contribution to the uncertainty of the final results.

ANTI-MALARIAL COMPOUND FROM THE STEM BARK OF Erythrina variegata Tati Herlina; Unang Supratman; M. S. Soedjanaatmadja; Anas Subarnas; Supriyatna Sutardjo; Noor Rain Abdullah; Hideo Hayashi
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

During the course of our continuing search for novel anti-malarial compounds from Indonesian plants, the methanol extract of the bark of E. variegata showed significant anti-malarial activity toward Plasmodium falciparum in vitro using the lactate dehydrogenase (LDH) assay. The methanol extract of the bark of E. variegata was separated by using bioassay-guide fractionation. The ethyl acetate fraction showed the most activity, exhibiting equipotency against both strains of parasite with IC50 of 23.8 µg/mL against 3D7 and 9.3 µg/mL against K1. Furthermore, by using the anti-malarial activity to follow separation, the ethyl acetate fraction was separated by combination of column chromatography to yield an active compound. The chemical structure of active compound was determined on the basis of spectroscopic evidences and comparison with those previously reported and identified as an isoflavonoid, warangalone. The warangalone showed anti-malarial activity against both strains of parasite used with IC50 of 4.8 µg/mL against 3D7 and 3.7 µg/mL against K1.

PREPARATION, CHARACTERIZATION AND CATALYTIC ACTIVITY TEST OF CoMo/ZnO CATALYST ON ETHANOL CONVERSION USING STEAM REFORMING METHOD Wega Trisunaryanti; Handirofa Handirofa; Triyono Triyono; Suryo Purwono
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

Preparation, characterization and catalytic activity test of CoMo/ZnO catalyst for steam reforming of ethanol have been investigated. The catalysts preparation was carried out by impregnation of Co and/or Mo onto ZnO sample. Water excess was used in ethanol feed for steam reforming process under mol ratio of ethanol:water (1:10). Characterizations of catalysts were conducted by analysis of metal content using Atomic Absorption Spectroscopy (AAS). Determination of catalysts acidity was conducted by gravimetric method of adsorption of pyridine base. Catalytic activity test on ethanol conversion using steam reforming method was conducted in a semi-flow reactor system, at a temperature of 400 oC, for 1.5 h under N2 flow rate of 10 mL/min. Gas product was analyzed by gas chromatograph with TCD system. The results of catalysts characterizations showed that the impregnation of Co and/or Mo metals on ZnO sample increased its acidity and specific surface area. The content of Co in Co/ZnO and CoMo/ZnO catalysts was 1.14 and 0.49 wt%. The Mo content in CoMo/ZnO catalyst was 0.36 wt%. The catalytic activity test result on ethanol conversion showed that the ZnO, Co/ZnO, and CoMo/ZnO catalysts produced gas fraction of 16.73, 28.53, and 35.53 wt%, respectively. The coke production of ZnO, Co/ZnO, and CoMo/ZnO catalysts was 0.86, 0.24, and 0.08 wt%, respectively. The gas products consisted mainly of hydrogen.

MEASUREMENT OF DISSOLVED INORGANIC NUTRIENT IN EUPHOTIC ZONE THE BANTEN BAY Alianto Alianto; Enan M. Adiwilaga; Ario Damar; Enang Harris
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

At a few this last years, measurement concentration of dissolved inorganic nutrient is has rapidlyed grow by using various methods. But method anything applied must based on at formation of indicator end of measurement amonia, nitrite, nitrate, orthophosphate and silicate. At measurement of amonia its indicator is formation of blue indophenol, nitrite formation of pink azo, nitrate formation of yellow colored solution, orthophosphate formation of blue molybdenum, and silicate based on formation of yellows silicomolibdate. The intensity of color that is highly dependent on the concentration of each element. Measurement of amonia blue indophenol intensity perfected concentration in the range 0.206-0.396 mg/L. Measurement nitrite the formation of a pink azo easy imperfect because its low concentration. Intensity measurements nitrate solution yellow perfect concentration in the range 0.128-0.989 mg/L. Measurement of imperfect blue molybdenum intensity orthophosphate because its low concentration. While measuring the formation silicate of yellow silicomolibdate perfect concentration on the range 10.573-26.470 mg/L. As a whole from result of measurement is obtained chemical composition of dissolved inorganic nutrient in euphotic zone the Banten bay is more predominated by silicate 97.27%, nitrate 1.84%, amonia 0.49%, orthophosphate 0.20%, and nitrite 0.18%.

SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL ACTIVITY OF FRIEDELIN [2, 3-d] SELENADIAZOLE Mehtab Parveen; Sayed Hasan Mehdi; Raza Murad Ghalib; Mahboob Alam; Rokiah Hashim; Othman Sulaiman
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

The new 1, 2, 3, selenadiazole derivative (3) was prepared from friedelin (1) via the corresponding semicarbazone (2) using Lalezari cyclization. The compounds were prepared, separated and characterized on the basis of microanalysis and spectral studies. The isolated friedelin and its selenadiazole were screened in vitro for their antimicrobial activities against various pathogenic bacterial were found to be highly active against all the selected pathogens. Compound 3 showed an inhibition zone of 14 mm and 12 mm respectively against highly resistant S. albus and C. albicans. A general mechanistic scheme for these reactions is also suggested based on current and previous results.

SYNTHESIS ALKANOLAMIDE TETRAHIDROXY OCTADECANOATE COMPOUND FROM CANDLE NUT OIL Daniel Daniel
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

Candle nut oil could be transesterificated by methanol with concentrated H2SO4 as a catalyst to form fatty acid methyl esther. Methyl linoleate could be separated by Column Chromatography mechanism technic partition from fatty acid methyl ester (FAME) mixture, then it was treated by ethanolamine at base condition in benzene as solvent and sodium methylate as a catalyst at reflux condition for 6 hours to form an alkanolamide. Alkanolamide could be epoxydized by tert-buthyl hydroperoxyde and peroxygenase as a catalyst and it was refluxed for 6 hours at 40 °C and nitrogen gas condition to form the epoxy alkanolamide octadecanoate, and then it was hydrolyzed by HCl 0.1 M to form alkanolamide tetrahidroxy octadecanoate (Polyol). Alkanolamide tetrahidroxy octadecanoate could be separated by Column Chromatography using silica gel H 40 and the eluent was the mixture of chloroform, ethyl acetate, formic acid in a ratio 90:10:1 (v/v/v/). Determination of HLB value from alknolamide tetrahydroxy octadecanoate is 13.096. Therefore, this compound was particularly suitable for application as an o/w emulsifiers. All af the reaction steps were confirmed by using FT-IR, 1H-NMR, GC-MS, Gas Chromatography and TLC.

DIFFERENTIAL PULSE ANODIC STRIPPING VOLTAMMETRY FOR DETERMINATION OF SOME HEAVY METALS IN URANIUM Saryati Saryati
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

The direct determination of some metals impurity in uranium by using differential pulse anodic stripping voltammetry (DPASV) method at a hanging mercury drop electrode and in a carbonate buffer media was developed. It was found that the carbonate buffer show the strongest affinity for uranium and gives the best separation between the DPASV peaks of heavy metals impurities. The carbonate concentration markedly affects the oxidation and reduction the major and the minor constituents of the uranium samples. In 0.1 M carbonate buffer solution pH 10, copper, bismuth, thalium, lead, cadmium, zinc, could be determined without the removal of the uranium matrix. Recovery and relative standard deviation (RSD) of this method was in the range of 174% - 85.2% for recovery and 36.8% - 1.2% for RSD. The larger error of analytical result was obtained for Zn at low concentration. In general, the analytic results error and RSD decreased with increasing metals concentration.

PHENOLIC COMPOUND FROM THE STEM BARK OF MANGGIS HUTAN (Garcinia bancana Miq.) AND THEIR ANTIOXIDANT ACTIVITY Muharni Muharni; Supriyatna Supriyatna; Husein H. Bahti; Dachriyanus Dachriyanus
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

A phenolic compoud, (-)-epicatechin, was isolated from the stem bark of Garcinia bancana. The structure of this compound was determined base on spectroscopic data such as including UV, IR, 1-D, 2-D NMR, and comparison with the reported data. Biological activity of this compound at free radical scavenging activity by 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) and inhibitory xanthine oxidase(XO) activity showed that (-)- epicathechin active at two methods with IC50 value 8.1 and 8.6 mg/mL respectively.

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