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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).
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Articles 21 Documents
Search results for , issue "Vol 6, No 2 (2006)" : 21 Documents clear
THE EXTRACTION OF NICKEL(II) AND COPPER(II) USING LIQUID MEMBRANE EMULSION TECHNIQUE Pirim Setiarso; Selvi Purwanti N.
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (164.951 KB) | DOI: 10.22146/ijc.21758

Abstract

Research on the extraction of Nickel(II) and Copper(II) using liquid membrane emulsion technique has been conducted. The purpose of this research is to know the influence of pH, extraction time and presence of competed metals (Ni2+ in Cu2+ and vice versa) toward the membrane extraction capability. In this research, 84 mL of Ni2+ and Cu2+ with concentration of 100 ppm, each, was extracted using pH variation (4.0, 4.5, 5.0, 5.5, 6.0). The optimum pH will be used to obtain the time of equilibrium and influence of the competed ions. Time variations (15, 20, 25, 30, 35 minute) were used with the concentration of the competed ions of 20, 40, 60, 80, 100 ppm. The percentage of ions extracted was analyzed by Atomic Absorption Spectrometry. The result shows that the optimum pH was 5.0 for extracting 79.3137 % Cu2+ and 50.3448 % Ni2+. Time of equilibrium was 30 minutes for extracting  85.4117 % Cu2+ and 53.7691 % Ni2+. The presence of Ni2+ influenced Cu2+ extracted and vice versa.
A NEW CLASS OF IONIC SOLVENTS, ELECTROLYTES AND ENGINEERING FLUIDS BASED ON 1,3-ALKYLMETHYL-1,2,3-BENZOTRIAZOLIUM SALTS Ahmad Mudzakir
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (537.102 KB) | DOI: 10.22146/ijc.21744

Abstract

A new series of ionic liquids based on 1,3-alkylmethyl-1,2,3-benzotriazolium cation has been prepared. The spectroscopic, physical and electrochemical characteristics of this family of salts have been investigated with respect to potential usage as ionic solvents, electrolytes and engineering fluids. Incorporation of diverse anions including weak coordinating anion and pseudohalide with this benzotriazolium cation produces ionic liquids with advantageously low melting points and good thermal stability. Thermal analyses of these very stable salts included the determination of melting points (-65 to 164 oC) and decomposition temperatures (up to 291 oC). The electrochemical windows of representative benzotriazolium species has been investigated by cyclic voltammetry and determined to be ~ 3 V. The X-ray single crystal and spectroscopic studies revealed that weak hydrogen-bonding interactions between the benzotriazolium ring protons and the anions are present both in the solid state as well as in solution.
SQUARE WAVE CATHODIC STRIPPING VOLTAMMETRY ADSORPTIVE FOR NICKEL AND COBALT ANALYSIS Saryati Saryati; Sumardjo Sumardjo
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (322.921 KB) | DOI: 10.22146/ijc.21753

Abstract

The adsorptive stripping voltammetric determination of Ni and Co based on adsorption of the Ni/Co and dimethylglioxime (DMG) complex on a hanging mercury drop electrode is studied. The reduction current of the adsorbed DMG complex is measured by square wave cathodic stripping voltammetry method. The effect of various parameters such as ligand concentration, pH of supporting electrolytic, adsorption potential and adsorption time on the current peak of Ni and Co voltammogram were studied. Optimum condition of this method are supporting electrolyte pH 9, DMG concentration 5×10 -4 M, adsorption potential -0.7 V vs Ag/AgCl and adsorption time 180 second. A linier relationship between the current peak and Ni or Co concentration was obtained in the range 5 - 30 ng/mL and the detection limit 0.6 ng/ml for both Ni and Co. The recovery of Ni and Co were 98.11-104.17% using standard biological materials with RSD 2.59 - 10.37%. Based on ";t"; test can be conclude that the result are nearly equal to the standard reference material.
THE UTILIZATION OF THERMOPHILIC PROTEASE WHICH LIFE IN HOT SPRING CANGAR BATU MALANG Rudiana Agustini
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (391.395 KB) | DOI: 10.22146/ijc.21762

Abstract

Thermophile protease has economic value, because this enzyme is useful on all kind of industry that used high temperature on it production process. The thermophile has been isolated from hot water spring at Cangar Batu Malang called CG-10 isolate. The characteristic of CG-10 are; bolt colony has a brown-white colour, rod form cels with size 6-14 µm and Gram positive. Identification with 16S-rRNA gene of their isolate shows 98.305% similarity with B. caldoxylolyticus. The protease characteristic of CG-10 isolate, fractionated by ammonium sulfate 35% (w/v), centrifuged by 4000 rpm of speed for 15 minute, (1) has optimum temperature of 80oC; (2) has optimum pH 8, (3) can survive until 60 minutes of incubation time at temperature 80oC , (4) the molecule weight of: 60-76 kDa with pH1 value between 7.5 - 8.20, (5) this protease is alkaline serine protease, and (6)Vmaks value 0.622 unit menit -1 and KM 9.8 µmol/L, so this CG-10 isolate protease can be use in detergent industry.
EFFECT OF ZEOLITE 4A ON WATER CONCENTRATION IN THE SYSTEM OF THE ESTERIFICATION REACTION OF ACETIC ACID WITH 1-BUTANOL Ratna Dewi Kusumaningtyas
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (307.547 KB) | DOI: 10.22146/ijc.21748

Abstract

The usual problem encountered on a reversible reaction is that the reaction cannot achieve a complete conversion of reactants since it is limited by the thermodynamic equilibrium. Due to this low conversion, it will face challenges with product purification and recycling of the reactants, which then cause an increase in the operation cost. To obtain higher conversion, it is necessary to shift the equilibrium towards the products by continuously removing the water formed. One popular example of reversible reaction is esterification process. In this research, water removal was conducted through an adsorption process using zeolite 4A. Effect of zeolite 4A on water concentration in the liquid phase esterification of acetic acid and 1-butanol catalyzed by sulfuric acid was investigated. It was performed in an isothermal batch reactor. The molar ratio of 1-butanol - acetic acid was 1.4 times theoretically, the catalyst concentration was 1 % wt and the mixing intensity was 1000 rpm. The influence of the temperature was studied at 40 to 80 °C and the zeolite 4A loading was varied at 1.6 to 5.52 % w/ v. The reaction was compared to the conventional esterification reaction carried out under identical conditions but without addition of zeolite 4A. Concentration of each component in the system was analyzed using on-line Gas Chromatography. Effect of removing the water produced during the reaction by using zeolite 4A was demonstrated. It was revealed that the amount of water removed was proportional to the amount of the zeolite 4A to be employed. On the other hand, the increase of the temperature led to the lower amount of water to be adsorbed. Among all the experiments, the best result was achieved on the addition of 5.52 % b/v zeolite 4A at 40 °C, where water concentration was 3.1356 g mole/L and the conversion was 76.11 % at the equilibrium condition. As comparison, water concentration on the conventional reaction performed at 40 °C was 6.9161 g mole/L and the conversion was 62.5 % at the equilibrium condition. The equation illustrating the effect of zeolite 4A loading on the conversion obtained at the equilibrium condition was: XAe = 0.6248 + 0.0868 C4A0.2848, where XAe was equilibrium conversion of Acetic Acid and C4A was Zeolite 4A loading (g/100 mL liquid).
SYNTHESIS OF THIN FILM OF TiO2 ON GRAPHITE SUBSTRATE BY CHEMICAL BATH DEPOSITION Fitria Rahmawati; Sayekti Wahyuningsih; Pamularsih A.W
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1068.652 KB) | DOI: 10.22146/ijc.21746

Abstract

Thin film of TiO2 on graphite substrat has been prepared by means of chemical bath deposition. Cetyltrimethylammonium Bromide served  as linking agent of synthesized TiO2 to graphite substrate.The optical microscope and Scanning Electron Microscope (SEM) indicate that surfactant concentration affects the pore morphology of thin film Surface Area Analysis (SAA) of thin film indicated that the pore of thin film included in mesopore category. The anatase phase of TiO2 quantity arised as the surfactant concentration increase, gave high efficiency of induced photon conversion to current efficiency (% IPCE).
STUDY ON EFFECT OF pH AND METAL CONCENTRATION ON THE SYNTHESIS OF DIMENSIONALLY STABLE ANODE GAPHITE/La2O3-ZrO2 AND GAPHITE/RuO2-TiO2 Suyanta Suyanta; Agus Kuncaka
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (213.623 KB) | DOI: 10.22146/ijc.21747

Abstract

The objective of this research is to study the effect of pH and metal concentration toward the mass of metal oxides coated on gaphite in the synthesis of dimensionally stable anode (DSA) gaphite/La2O3-ZrO2 and gaphite/RuO2-TiO2. The synthesis of those  DSA was done by thermal decomposition technique. The solution containing metal ion to be coated (as its oxides) on the gaphite, followed by heating. Those spraying and heating were repeated up to ten times, so that it was expected that all of gaphite surface was covered by the metal oxides. It was concluded that the mass of metal oxides coated on the gaphite was affected by the pH and concentration of metals in the solutian to be sprayed. Treatment by using solution at pH of 4 and 6 produced  more in mass of metal oxides mixture than  using solution of 1 and 2 on pHs. DSA gaphite/La2O3-ZrO2 produced by treatment using solution of 4 and 6 on pHs contained more in mass of La2O3 than of ZrO2; meanwhile DSA gaphite/RuO2-TiO2 produced in this research (for all of treatment) contained more in mass of RuO2 than of TiO2.
A NOVEL METHOD OF THE HYDRIDE SEPARATION FOR THE DETERMINATION OF ARSENIC AND ANTIMONY BY AAS Ganden Supriyanto; Jürgen Simon
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (258.4 KB) | DOI: 10.22146/ijc.21752

Abstract

A novel method is proposed for the hydride separation when determinining of arsenic and antimony by AAS. A chromatomembrane cell was used as preconcentration-, extraction- and separation-manifold instead of the U-tube phase separator, which is normally fitted in continuous flow vapour systems generating conventionaly the hydrides. The absorbances of the hydrides produced were measured by an atomic absorption spectrophotometer at 193.7 nm and 217.6 nm. Under optimized analytical conditions, the calibration plot for arsenic was linear from 50 to 500 ng.mL-1 (r2 = 0.9982). The precision for three subsequent measurements of 500 ng.mL-1 arsenic gave rise to a relative standard deviation of 0.4%. The detection limit was 15 ng.mL-1, which is much lower compared with that of the conventional hydride system (2000 ng.mL-1). A similar result was observed in case of antimony: the detection limit was 8 ng.mL-1 when the proposed method was applied. Consequently, the sensitivity of the novel method surpasses systems with conventional hydride generation, i.e. the precision and the acuracy increase whereas the standard deviation and the detection limit decrease. The proposed method was applied in pharmacheutial analysis and the certified As-content of a commercial product was very sufficiently confirmed.
INVESTIGATION OF DISSOLVED SULPHATE IN VARIOUS GEOTHERMAL FIELDS OF SUMATRA USING OXYGEN AND SULPHUR ISOTOPES E. Ristin Pujiindiyati; Zainal Abidin
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (270.027 KB) | DOI: 10.22146/ijc.21756

Abstract

There are at least 30 high temperature systems; eleven active volcanoes, five degassing volcanoes and one caldera volcano controlled by Sumatra Fault Zone over a length of 1700 km. To understand this geothermal field system, some information about geochemistry including isotope composition in its fluid is needed. Sulphur-34 and oxygen-18 isotopes in dissolved sulphate pair have been used to determine the origin of acidic fluid of sulphate and to evaluate the process involved. The fluids from eight hot springs, two fumaroles, four deep wells and crater have been collected in along Sumatra geothermal fields. Sulphur-34 (d 34S (SO4), 0/00 CDT) and oxygen-18 (d 18O (SO4), 0/00 SMOW) in sulphate is analyzed according to Robinson-Kusakabe and Rafter method, respectively. The d 34S (SO4) values from Sibayak wells are more enriched of 16.8 0/00 to 18.2 0/0 that may indicate the dissolution of anhydrite minerals or isotope partitioning in hydration of SO2. The d 34S (SO4) values from two fumaroles (Pusuk Bukit - North Sumatra and Rantau Dadap - South Sumatra) are at depleted value of -0.150/00 and 1.80/00, those are close to d 34S from magmatic sulphur.  In general, the d 34S (SO4) of springs spread in a wide range of 5.250/00 to14.20/00 and show a mixing process between atmospheric sulphate and sulphate from deep wells. The d 18O (SO4) from wells exhibits depleted value around -3.60/00 suggesting that 87.5% of sulphate oxygen is derived from groundwater oxygen and 12.5% is derived from atmospheric molecular oxygen in sulphide oxidation reaction. In the other hand, hot springs (except Semurup), crater and fumaroles have enriched value of d 18O (SO4). These enriched values suggest that a higher percentage of atmospherically derived oxygen compared to those from the depth.
CAPILLARY ELECTROPHORETIC ANALYSIS OF LOW-MOLECULAR-MASS OF CA SPECIES IN PHLOEM SAP OF Ricinus communis L. Noor Fitri; Björn Thiele; Klaus Günther; Buchari Buchari
Indonesian Journal of Chemistry Vol 6, No 2 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (698.628 KB) | DOI: 10.22146/ijc.21757

Abstract

A capillary electrophoretic (CE) analysis with ultra-violet (UV) detection was performed for further separation of low-molecular-mass (LMM) calcium species in phloem sap of Ricinus communis L. Two different background electrolytes (BGE) were used for the separation; these are (1) hydrogen phosphate/dihydrogen phosphate buffer containing cetyltrimethylammonium bromide (CTAB) as an electro-osmotic flow (EOF) modifier, and (2) boric acid buffer containing CTAB. Various parameters affecting the analysis, including the composition and pH of the BGE were systematically studied. The sensitivity, resolution, baseline noise, migration time of the species peaks, and reproducibility of the method were evaluated under optimised condition. At least 13 UV-active species were optimally separated within about ten minutes. The optimised measurement condition was also achieved using 10 mM hydrogen phosphate/10 mM dihydrogen phosphate containing 0.5 mM CTAB at pH 8.0 as BGE, and by applying voltage of ‑20 kV and temperature of 14°C. Evidently, the analytical method was successfully used for the separation of LMM calcium species in phloem sap of R. communis L.

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