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INDONESIA
Indonesian Journal of Chemistry
ISSN : 14119420     EISSN : 24601578     DOI : -
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).
Arjuna Subject : -
Articles 1,981 Documents
A NOVEL OCTAHEDRAL NIOBIUM OXYCHLORIDE CLUSTER BUILT FROM INTERCONNECTED Nb6Cl12O4 UNITS: Cs2Sc3Nb12 Fakhili Gulo
Indonesian Journal of Chemistry Vol 11, No 2 (2011)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (816.912 KB) | DOI: 10.22146/ijc.21396

Abstract

A novel octahedral niobium cluster oxychloride compound, Cs2Sc3Nb12Cl27O8 was synthesized by solid-state route techniques from stoichiometric mixture of CsCl, Sc2O3, Nb, NbCl5, and Nb2O5, heated at 700 °C for two days. The crystal structure was determined by single crystal X-ray diffraction method. It crystallizes in orthorhombic system with space group of Pnma, a = 17.5206(1) Å, b = 29.6899(3) Å, c = 9.2114(1) Å, and V = 4791.63(8) Å3. The structure is based on  unit in which four oxygen ligands selectively occupy inner positions arranged in sets of three and one on opposite side of the Nb6 octahedron. Each cluster shares three apical-chlorine ligands with three adjacent clusters to form layers with topology similar to that of graphite. The cluster units are also connected to each other by both cesium and scandium atoms to form a three-dimensional framework. This compound exhibits 14 valence electrons per cluster.
SYNTHESIS OF COPPER OXIDE NANO PARTICLES BY USING Phormidium cyanobacterium Abdul Rahman; Amri Ismail; Desi Jumbianti; Stella Magdalena; Hanggara Sudrajat
Indonesian Journal of Chemistry Vol 9, No 3 (2009)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (360.079 KB) | DOI: 10.22146/ijc.21498

Abstract

In this paper, we report a suitable method for extracellular synthesis of copper oxide nano particles by using Phormidium cyanobacterium. We hypothesize that synthesis of copper oxide nano particles is believed to occur by extracellular hydrolysis of the cationic copper by certain metal chelating anionic proteins/reductase secreted by bacteria under simple experimental conditions like aerobic environment, neutral pH and room temperature. Proteins not only reduce Cu (II) into copper oxide nano particles (CONPs) but also plays significant role in stabilization of formed nanoparticles at room temperature. Further TEM, SEM, XRD and FTIR analysis have confirmed the synthesis of nano particles through microbial route. Extracellular induction of metal chelating proteins/reductase was analyzed by SDS-PAGE.
SILVER RECYCLING FROM PHOTO-PROCESSING WASTE USING ELECTRODEPOSITION METHOD Mochammad Feri Hadiyanto; Agus Kuncaka
Indonesian Journal of Chemistry Vol 2, No 2 (2002)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (49.354 KB) | DOI: 10.22146/ijc.21921

Abstract

            Silver electrodeposition of photo-processing waste and without addition of KCN 1,0 M has been studied for silver recycling. Photo procesing waste containing silver in form of [Ag(S2O3)2]3- was electrolysed at constant potential and faradic efficiency was determined at various of electrolysis times. Electrolysis of 100 mL photo processing waste without addition of KCN 1,0 M was carried out at constant potential 1.20 Volt, while electrolysis 100 mL photo procesing waste with addition of 10 mL KCN 1,0 M electrolysis was done at 1.30 Volt.The results showed that for silver electrodeposition from photo processing waste with addition of KCN 1,0 M was more favorable with faradic efficiency respectively were 93,16; 87,02; 74,74 and 78,35% for 30; 60; 90 and 120 minutes of electrolysis.
INTERCALATION OF OLYGOMER OF HYDROXYL-CHROMIUM INTO NATURAL KAOLINITE Rodiansono Rodiansono; Reda Ariyantie; Abdullah Abdullah
Indonesian Journal of Chemistry Vol 8, No 1 (2008)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (2322.666 KB) | DOI: 10.22146/ijc.21644

Abstract

Preparation of a kaolin-hydroxyl chromium composite and characterization of its physico-chemical properties were conducted. The olygomer hydroxyl-chromium was prepared by adding Na2CO3 to 0.1 M chromium nitrate solution (ratio OH/Cr = 2) and then dried at 110 oC and 400 oC for 4 h. Characterization of kaolin-hydroxyl chromium composite includes determination of acidity, functional groups, basal spacing, and surface area (BET-N2 sorption analyzer). The result showed that intercalation of hydroxyl chromium resulted in the decreasing of basal spacing but increased the specific surface area of kaolin. Drying of the intercalated kaolin at 400 oC decreased surface area, total volume pore and pore radius. FT-IR spectra showed that hydroxyl-chromium detected at wavelength of 2925 and 2855 cm-1.
SYNTHESIS OF NANOPARTICLE SEMICONDUCTOR CdS IN PHASE TRANSFORMED MICROEMULSION OF WATER/ SDS/ ETANOL/ n-HEXANE SYSTEM Fitria Rahmawati; Abu Masykur; Heni Worowidiyanti
Indonesian Journal of Chemistry Vol 5, No 2 (2005)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1809.268 KB) | DOI: 10.22146/ijc.21812

Abstract

The objective of this research is to study wheather the emulsion system of water/SDS (Sodium Dodecyl Sulphate)/ethanol/n-hexane can be transformed from S1 (hydrocarbon in water) type to S2 (water in hydrocarbon). CdS can be synthesized in the transformed product of microemulsion medium. The emulsion type transformation from S1 to S2 was conducted by adding n-hexane increment of 5 mL as hydrocarbon phase and stirring at 300 rpm for 2 minutes. The inversion point was defined from the measurement of emulsion conductivity and was supported by data of the droplet view under optical microscope. CdS was synthesized from reaction of Cd(NO3)2.4H2O with Na2S in phase transformed microemulsion medium. CdS cluster size was obtained from its UV-Vis spectrum and was characterized using X-ray diffraction to analyse the crystallinity and crystal system, then the influence of the variation of SDS amount to the CdS cluster size and its UV-Vis spectrum was observed.The result of this research shows that the system of n-hexane/SDS/water emulsion can be transformed from S1 to S2 type. The SDS amount in the microemulsion has influence the CdS cluster size. The larger amount of SDS added, the smaller of CdS cluster size was obtained. XRD data indicated that CdS cluster has been obtained with 40.613 % of purity.
THE PREPARATION OF AN IODATE SELECTIVE ELECTRODE USING SILVER IODATE AS THE ACTIVE AGENT IN A CHITOSAN SUPPORT Ani Mulyasuryani; Qonitah Fardiyah; Rizki Sugiri
Indonesian Journal of Chemistry Vol 7, No 3 (2007)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (127.983 KB) | DOI: 10.22146/ijc.21670

Abstract

The iodate-selective electrode based on the principle of precipitation reaction could be made by coating the platinum wire with silver iodate (AgIO3). In this research was carried out optimization the iodate-selective electrode using chitosan membrane as an AgIO3 support. The AgIO3 were added in the 2 mL 1% chitosan solution, is 0.5 to 2.5 % (w/v). The thickness of the membrane used is 6 to 12 µm. The electrode cell potential is measured against Ag/AgCl electrode as a reference electrode. The optimum electrode performance was at 2.0 % of AgIO3 with thickness a membrane of 10 µm. The iodate-selective electrode has a Nernstian factor is 52.96 mV/decade and a response time of 10 seconds. The concentration range was determined from 10-3 M to 10-1 M and the detection limit is 1.12 x 10-5 M.
KINETIC INVESTIGATION OF CARBON DIOXIDE, ACETIC ACID, ACRYLIC ACID FORMATION ON DILUTED AND LEACHED MoVTeNb CATALYST Restu Kartiko Widi
Indonesian Journal of Chemistry Vol 12, No 2 (2012)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (235.727 KB) | DOI: 10.22146/ijc.21352

Abstract

Reaction kinetics for the oxidation of propane over diluted-leached MoVTeNb is described. This paper is focused on the study of determination of the orders of carbon dioxide, acetic acid and acrylic acid formation. Deep oxidation of propane to carbon dioxide is first order with respect to hydrocarbon, and partial order (0.31) with respect to oxygen. The selective oxidation of propane to acrylic acid is partial order (0.49) with respect to hydrocarbon and partial order (0.09) with respect to oxygen.
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

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (278.555 KB) | DOI: 10.22146/ijc.21537

Abstract

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.
Preparation of Peleted Ni-Pt/Zeolite for Conversion of Amyl and Isoamyl Alcohol to Hydrocarbon Abdullah Abdullah; Triyono Triyono; Bambang Setiaji
Indonesian Journal of Chemistry Vol 1, No 2 (2001)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (6301.581 KB) | DOI: 10.22146/ijc.21944

Abstract

Catalysts with Ni and Pt as active metals in peleted zeolite were used for conversion of amyl alcohol, isoamyl alcohol and their mixture to hydrocarbon compounds. The catalysts were prepared by impregnation the peleted zeolite in NiCl2.6H2O and PtCI4 solution, while stirring for 24 hours then followed by oxidation with 02 gas at 350 °C for 2 hours and reduced by hydrogen gas at 400 °C for 1 hour. Ni and Pt in catalysts were determined by MS, specific surface area, total pore volume and gas sorption analyzer NOVA-1000 determined pore radius average. Determination of catalysts acidity was carried out by absorption of ammonia method. The activity of catalysts was evaluated in a micro reactor by flow system. Experimental temperature by varied between 300 and 400 °C with the increment of 25 °C. Products were analyzed by gas chromatographic and mass spectrometric method. The result shows that Ni-Pt/zeolite is more active than Ni/zeolite can be used for converting all of the alcohol. Products for conversion are 2-pentene, 2-methyl-1-butene, 2-methyl-2-butene, cyclopentane, 3-methyl-1-butanaldehide and acetone. The highest conversion was observed on isoamyl alcohol (31.37%) at 400 °C.
MACRONONE, A NOVEL DIEPOXYLIGNAN FROM BARK OF MAHKOTA DEWA (Phaleria macrocarpa (Scheff.) Boerl.) AND ITS ANTIOXIDANT ACTIVITY Susilawati Susilawati; Sabirin Matsjeh; Harno Dwi Pranowo; Chairil Anwar
Indonesian Journal of Chemistry Vol 12, No 1 (2012)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (655.052 KB) | DOI: 10.22146/ijc.21373

Abstract

Mahkota dewa (Phaleria macrocarpa (Scheff.) Boerl.) which is belong to family of Thymelaeaceae is one of Indonesian traditional medicines. Chemical constituent has been isolated from bark of mahkota dewa. Sample was extracted with methanol. Concentrated methanol extract was extracted by n-hexane, chloroform and ethyl acetate. A Compound that separated and purified by column chromatography from ethyl acetate extract is a red spherical crystal (m.p. 94-95 °C). Its spot gave yellow fluorescence at TLC plate (UV366) and has optical rotation of -9.3°(c. 2 mg/mL, methanol). Structure elucidation by UV, IR, 1H-NMR, 13C-NMR and NMR 2 dimension (HMQC, COSY, HMBC and DEPT-135) spectroscopy show that the compound gives a name macronone. Computational chemistry calculation using Hyperchem on the level of semiempirical method PM3 was confirmed the conformation of macronone. DPPH method shows that macronone has lower antioxidant activity compare to the ethyl acetate extract.

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