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Indonesian Journal of Chemistry

ijc
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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 10 Documents

Search results for , issue "Vol 4, No 2 (2004)" : 10 Documents clear

CYTOTOXICITY IDENTIFICATION OF THE SUPERNATANT OF Manihot esculenta Crantz RHIZOME AS RIBOSOME-INACTIVATING PROTEIN TO NORMAL CELL Endang Astuti; Sabirin Matsjeh; Winarto Haryadi; Deni Pranowo; Nuning Sri Mulatsih
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

The supernatant of Manihot esculenta Crantz rhizome has been used as an alternative remedy of infectious and cancer in Jogjakarta. Cytotoxicity assay showed that Manihot esculenta Crantz supernatant had cytotoxic effect to cancer cell line, namely Myeloma (LC50 = 180,24 μg/mL) and HeLa (LC50 = 415,55 μg/mL), but have a little cytotoxic effect to SiHa. This research was aimed to identify cytotoxic activity of Manihot esculenta Crantz's supernatant to normal cell, particularly to human mononuclear cell and Vero cell line, and to compare to the cancer cell lines. The result showed that supernatant of M. esculenta had cytotoxic effect to normal mononuclear cell (LC50 = 564,00 μg/mL) and Vero cell line (LC50 = 686,00 μg/mL). The supernatant of M. esculenta had the highest cytotoxic activity to myeloma and relatively toxic to cervix cancer HeLa and normal cell, but less to SiHa.

THE STEREOCHEMISTRY EFFECT OF EUGENOL, CIS-ISOEUGENOL AND TRANS-ISOEUGENOL ON THEIR CATALYTIC HIDROGENATION M. Muchalal
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

The stereochemistry effect of eugenol, cis-isoeugenol and trans-isoeugenol on their catalytic hydrogenation by Ni/g-Al2O3 catalyst was investigated. In this investigation, the catalyst is prepared by impregnation of Nickel into solid of γ-Al2O3 in methanol as a solvent. The calcination process, which is followed by reduction, is performed on Muchalal reactor at 400 oC. After that, the catalytic hydrogenation is carried out under hydrogen gas atmosphere by mixing 10 mL sample and 0.5 g Ni/g-Al2O3 catalyst at 200 oC for 3 hours. The stereochemistry effect of reactants is evaluated by computer modelling using PM3 semiempirical methods. The mass spectrum of catalytic hydrogenation product from those compounds shows a molecular ion at m/z 164, which proves the existence of 2 -methoxy-4-propylphenol. The eugenol gives the highest conversion (99%), followed by cis-isoeugenol (81%) and trans-isoeugenol (67%). It was found that there is a correlation between the stereochemistry of those compounds and catalytic reactivity.

UTILIZATION OF ACTIVATED ZEOLITE AS MOLECULAR SIEVE IN CHROMATOGRAPHIC COLUMN FOR SEPARATION OF COAL TAR COMPOUNDS Dwi Retno Nurotul Wahidiyah; Bambang Setiaji; Iqmal Tahir
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

Application of activated zeolite (ZAA) as molecular sieve to separate compounds of coal tar from vaccum fractional distillation, have been done. The size of zeolite was 10-20 mesh and used as solid phase in column chromatography with length of 30 cm. The first step of the research was coal pyrolisis and the product (tar) was distillated by fractional column and vaccum system at reduced pressure 44 cmHg and maximum temperature at 200 oC. The distillate from this procedure was flowed to the column chromatography of zeolite (ZAA). The compound absorbed by zeolite was eluted with varying solvents, i.e: CCl4, acetone and ethanol. Each fraction was then analyzed by gas chromatography. The results showed, zeolite have a capability to separate the compounds of tar and it tends to absorb medium hydrocarbon. The nonpolar eluent [CCl4] gives the better result in eluting tar compound than polar (ethanol) or medium polar eluents (acetone).

STUDY OF EPOXIDE DECYCLISATION OF CARYOPHYLENE OXIDE WITH SYNTHETIC ZEOLITE AS CATALYSTS Winarto Haryadi; M. Muchalal
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

The reaction of epoxide ring opening of caryophillene oxide has been done using zeolite H-Y, H-sodalit, and H-ZSM-5 as catalysts. The reactions were done in two types, there were in dioxane solvent at temperature of 110 oC and without solvent at temperature of 175 oC. The catalyst weight was 10 % from caryophillene oxide weight, and the time of reaction was four hours. The product of reaction was analyzed using GC, FTIR, and GC-MS. The reactions of caryophillene oxide in dioxane solvent with the three kinds of zeolites did not give any targeted product. Whereas, the reactions without solvent gave three main products, there was one compound with one group of secondary hidroxyl (secondary alcohol), and two compounds of ketone from caryophillene. The reaction product of caryophillene oxide obtained without using solvent with the three type of catalysts were then compared. Conversion of three main products produced by H-ZSM-5 catalyst, H-sodalit catalyst and H-Y catalyst were 82.11 %, 54.92 % and 38.53 % respectively. For that reason, the transformation of caryophillene oxide using H-ZSM-5 catalyst was considered to be the best selective product. The alcohol product was resulted from reaction between caryophillene oxide and Bronsted acid, and the ketone products was resulted from the reaction with Lewis acid in zeolite.

A STUDY ON INTERACTION OF Cd(II) AND DIATOMACEOUS EARTH IN ADSORPTION PROCESS Nuryono Nuryono; Suyanta Suyanta
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

In this research, interaction occurring in adsorption process between Cd(II) and active site of diatomaceous earth has been studied. The study was carried out by evaluating Cd(II) adsorption on diatomaceous earth at various pHs, either for the earths without treatment, those after being heated or those treated with sulfuric acid and hydrogen chloride. Adsorption was performed by mixing diatomaceous earth, without and with treatments, and Cd(II) solution for one hour at various pHs (2 - 7), and un-adsorbed metallic ion was analyzed by atomic absorption spectroscopy (AAS). The treatments of diatomaceous earth included heating at temperatures of 300, 500, and 900oC for four hours, treatments with acids (3, 8, and 12 M of H2SO4, and 3, 15, and 18 M of HCl solutions for two hours at 150-200oC). Results showed that the increasing of pH from 2.0 to 3.0 and from 6.0 to 7.0 inclined adsorption of Cd(II) from 13.2 to 23.3 mg/g and from 24.0 to 26.4 mg/g, respectively. At a pH range of 3.0 - 6.0 the adsorption slightly increase from 23.3 to 24.0 mg/g. Heating of diatomaceous earth higher than 500oC caused the adsorption capability to be independence of the pH of solution. On the other hand, treatments with acids (H2SO4 and HCl) caused adsorption capability increased significantly with the increase in pH from 3.0 to 6.0. Adsorption evaluation at the pH range investigated showed that adsorption of Cd(II) on diatomaceous earth may be through interaction between Cd2+ and functional groups of T-OH (T = Si/Al).

THE DETERMINATION OF OPTIMUM CONDITION FOR THE SYNTHESIS OF ALKYL MONOETHANOLAMIDE FROM PALM KERNEL OIL Hilyati Hilyati; Wuryaningsih Wuryaningsih; M. Nasir; Tasrif Tasrif; T. Beuna
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

Synthesis of alkyl monoethanolamide from palm kernel oil was done by two steps reaction that are esterification and amidation. The esterification, that is the reaction between palm kernel oil and methanol with mole ratio of 1:3 using acid catalyst (H2SO4) 4 % at temperature 60 OC for two hours, results in methyl ester palm kernel oil. The methyl ester product was produced by amidation reaction on any variation of time, temperature, catalyst, catalyst concentration and ratio of the reactan. The best result of the synthesis (amide conversion of 98.15 %) was obtained at temperature of 160 OC for 6 hours with mole ratio of methyl ester palm kernel oil to ethanol amine (ratio of the reactan) 1:1 using KOH catalyst 0.5 % and H2SO4 catalyst 0.5 %.

STUDY OF ELECTROPOLIMERIZATION PROCESSES OF PYRROLE BY CYCLIC VOLTAMMETRIC TECHNIQUE Adhitasari Suratman; Buchari Buchari; Indra Noviandri; Suryo Gandasasmita
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

Electropolymerization processes and electrochemical properties of polypyrrole as electroactive polymer have been studied by cyclic voltammetric technique. Pyrrole was electropolymerized to form polypyrrole in water-based solvent containing sodium perchlorate as supporting electrolyte in several pH values. The pH of the solutions were varied by using Britton Robinson buffer. The results showed that oxidation potential limit of electropolymerization processes of pyrrole was 1220 mV vs Ag/AgCl reference electrode. It can be seen that cyclic voltammetric respon of polypyrrole membrane that was prepared by electropolymerization processes of pyrrole at the scanning rate of 100 mV/s was stable. While the processes of pyrrole electropolymerization carried out at the variation of pH showed that the best condition was at the pH range of 2 - 6.

SYNTHESIS OF ANTIMALARIAL 3-(2-HYDROXYETHYL)-2-METHYL-1,10-PHENANTHROLINE-4-OL FROM 8-AMINOQUINOLINE Ruslin Hadanu; Chairil Anwar; Jumina Jumina; Iqmal Tahir; Mustofa Mustofa
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

It has been conducted the synthesis of 3-(2-hydroxyethyl)-2-methyl-1,10-phenanthroline-4-ol was carried out from 8-aminoquinoline which are expected to posses antimalarial activity. The experiment perfomed consisted of two steps i.e (1) reaction of 8-aminoquinoline with 2-acetyl-butyrolactone and (2) cyclization of the resulted 3-[1-(quinolin-8-ylamino)-ethylidene]-4,5-dihydro-furan-2-one. The reaction of 8-aminoquinoline with 2-acetyl-butyrolactone was performed in toluene at reflux for 6 hours in the presence of p-toluensulfonic acid as catalyst. This reaction gave 3-[1-(quinolin-8-ilamino)-etiliden]-4,5-dihidro-furan-2-on in 60.6% yield. The cyclization of 3-[1-(quinoline-8-ylamino)-ethyliden]-4,5-dihydro-furan-2-one was conducted in cloroform at reflux for 4 hours in the presence of H2SO4 as catalyst and also tween 80 as transfer phase catalyst to give 3-(2-hydroxy-ethyl)-2-methyl-1,10-phenanthroline-4-ol in 76.2% yield. Identification of the products were carried out by means of infra red (IR) spectroscopy, proton nuclear magnetic resonance (1H-NMR) spectroscopy, and mass spectroscopy (MS).

GAS PHASE STRUCTURE AND STABILITY OF COMPLEX FORMED BY H2O, NH3, H2S AND THEIR METHYL DERIVATIVES WITH THE CATION CO2+ Cahyorini Kusumawardani
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

Ab initio molecular orbital calculations at the Hartree-Fock-Self Consistent Field (HF-SCF) have been performed in order to determine the structure and gas phase energies of complex formed by the Lewis bases of H2O, NH3, H2S and their methyl derivatives with the cation Co2+. The relative basicities of the base studied depend on both the substituent. The gas-phase interaction energies computed by the SCF method including electron correlation Møller-Plesset 2 (MP2) dan Configuration Iteration (CI) were comparable in accuracy. The binding energies computed by these two methods reach the targeted chemical accuracy.

THE STABILIZING OF ANATASE AEROGEL AT HIGH TEMPERATURE Silvester Tursiloadi; Hiroshi Hirashima
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

Stable anatase is attractive to its notable functions for photo catalysis and photon-electron transfer. Stable anatase TiO2 containing amorphous SiO2 aerogel was prepared by hydrolysis of Ti (OC3H7)4 and Si (OC3H7)4 in a 2-propanol solution with acid catalyst. The solvent in wet gels was supercritically extracted in CO2 at 60 oC and 22 Mpa. Thermal evolutions of the microstructure of the gels were evaluated by TGA-DTA, N2 adsorption and XRD. A stable anatase TiO2 containing amorphous SiO2 aerogel with a BET specific surface area of 365 m2/g and a total pore volume of 0.20 cm3/g was obtained as prepared condition. The anatase phase was stable after calcination up to 1000 oC, and BET specific surface area, total pore volume and average pore diameter did not change significantly after calcination up to 900 oC.

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