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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 22 Documents

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Search results for , issue "Vol 10, No 3 (2010)" : 22 Documents clear

ENHANCEMENT OF THE SENSITIVITY AND SELECTIVITY OF THE VOLTAMMETRIC SENSOR FOR URIC ACID USING MOLECULARLY IMPRINTED POLYMER Miratul Khasanah; Mudasir Mudasir; Agus Kuncaka; Eko Sugiharto; Ganden Supriyanto; Siti Wafiroh
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

The sensitivity and selectivity of voltammetric sensor for uric acid can be improved by modifying the working electrode using a polymer with a molecular template (molecularly imprinted polymer, MIP). Polymer and MIP was synthesized from methacrylic acid (MAA) as monomer, ethylene glycol dimethacrylic acid (EGDMA) as cross-linker, uric acid (UA) as template and the results were characterized by various methods. The poly-MAA formation was identified by a decrease in the intensity of infrared (IR) spectra at ~1540 cm-1 (C=C) and an increase at ~1700 cm-1 (C=O) compared to the IR spectra of the MAA and EGDMA. The SEM analysis showed that the cavity of polymer is small enough (~ 0.1 µm) and homogeneous. Establishment of MIP was carried out by extracting of the uric acid from the polymer network. The IR spectra of MIP exhibited the decrease in intensity at ~1700 cm-1 (C=O) compared to the non imprinted polymer (NIP). The data of BET analysis showed that polymer pore size increase slightly from 37.71 Å to 38.02 Å after the extraction process of uric acid from the polymer network. Its may be due to incomplete extraction of uric acid from the polymer network. Modifications of hanging mercury drop electrode using MIP made from MAA, EGDMA, and UA with a mole ratio of 1:3:1 produced a sensitive and selective voltammetric sensor for uric acid. The sensitivity obtained was 16.405 nA L/µg. The presence of ascorbic acid in equal concentration with uric acid decreased the current response of only 0.08%. Compared to HMDE electrode, the sensitivity and selectivity of the HMDE-MIP sensor enhanced about 100 and 700 times, respectively. The detection limit was found to be 5.94 x10-10 M.

STRUCTURE OF IRIDIUM(III) HYDRATION BASED ON AB INITIO QUANTUM MECHANICAL CHARGE FIELD MOLECULAR DYNAMICS SIMULATIONS Ponco Iswanto; Ria Armunanto; Harno D. Pranowo
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

Structural properties of Iridium(III) hydration have been studied based on an ab initio Quantum Mechanical Charge Field (QMCF) Molecular Dynamics (MD) Simulations. The most chemical-relevant region was treated by ab initio calculation at Hartree-Fock level. For the remaining region was calculated by Molecular Mechanics method. LANL2DZ ECP and DZP Dunning basis sets were applied to Ir3+ ion and water, respectively. The average distance of Ir-O in the first hydration shell is 2.03 Å. The QMCF MD Simulation can detect only one complex structure with coordination number of 6 in the first hydration shell. Bond angle analysis shows that Ir3+ ion hydration in the first hydration shell has octahedral structure.

ADSORPTION OF GIBBERELLIC ACID (GA3) ONTO ACID ACTIVATED KAOLIN Sunardi Sunardi; Yateman Yateman Arryanto; Sutarno Sutarno
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

Preparation, activation and adsorption study of natural kaolin from Tatakan, Tapin, South Kalimantan have been conducted. The activation of kaolin was done using 6 M HCl solutions at 90 °C for 3 h. The characterizations of kaolin were carried out by Fourier Transform Infrared, X-ray diffraction, and surface area analyzer. Adsorption parameters studied included the effect of pH, contact time, and concentration of gibberellic acid (GA3) onto kaolin samples. The amount of gibberellic acid adsorbed was determined using UV spectrophotometer. The adsorption capacity of kaolin was determined by Langmuir adsorption isotherm model. The result showed that activation of kaolin was resulted the larger specific surface area and more homogeneous composition of kaolin without any destruction of kaolin structure. Adsorption of gibberellic acid onto kaolin before and after activation showed that optimal adsorption was obtained at pH » 7 and reached the equilibrium within 4 h. The calculations result by Langmuir adsorption isotherm model showed that the increasing of adsorption capacity of acid activated kaolin is about 35%.

DETERMINATION OF CARBAMATE PESTICIDES USING A BIOSENSOR BASED ON ENZYME ACETYLCHOLINESTERASE AND CHOLIN OXIDASE ON PLATINUM ELECTRODE Mashuni Mashuni; M. Syahrul; A. Ahmad; A. W. Wahab
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

In recent years, instead of their potential hazard to human health, carbamic pesticides are widely used in agriculture. Therefore, there is a growing interest in rapid and accurate determination for food safety and environmental monitoring. The aim of this research is to designs a biosensor for analyzing carbamate pesticides residue in sample with composite variables of glutaraldehyde (GA) concentration in electrode membrane. Enzyme acetylcholinesterase (AChE) was co-immobilised with choline oxidase (ChO) onto a platinum (Pt) surface using a solution of 5%, 10%, 15% cellulose acetate and 25% glutaraldehyde. The result of this research show that detection limit of the sensor using cellulose acetate 5%, 10 % and 15 % are 10-7.7 M, 10-8.7 M and 10-7.6 M respectively. The results are approximately equal to 2.2 ppb-0.2 ppb, which means that this biosensor is very sensitive for determining carbamates pesticides residue. Detection limit of biosensors are comparable to that of the conventional instrument such as Gas Chromatography (GC) and High Pressure Liquid Chromatography (HPLC), i.e. 1.5 ppb and 2.0 ppb respectively. The proposed electrochemical pesticide sensitivity test exhibited high sensitivity, desirable accuracy, low cost and simplified procedure.

DOCKING OF 1-PHENYLSULFONAMIDE-3-TRIFLUOROMETHYL-5-PARABROMOPHENYL-PYRAZOLE TO CYCLOOXYGENASE-2 USING PLANTS Stefanus Layli Prasojo; Fajar Agung Dwi Hartanto; Nunung Yuniarti; Zullies Ikawati; Enade Perdana Istyastono
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

The docking protocols to virtually screen selective cyclooxygenase-2 (COX-2) ligands using PLANTS docking software were developed and validated. The crystal structure of 1-phenylsulfonamide-3-trifluoromethyl-5-parabromophenyl-pyrazole (S58) binds to cyclooxygenase-2 (COX-2) was used as the reference structure. The developed protocols could predict the binding pose of S58 to COX-2 accurately (RMSD is 1.2 Ǻ).

STUDY ON THE STRUCTURAL BASIS OF PERIPHERAL LIGHT HARVESTING COMPLEXES (LH2) IN PURPLE NON-SULPHUR PHOTOSYNTHETIC BACTERIA Tatas H.P. Brotosudarmo; Richard J. Cogdell
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

Photosynthesis provides an example of a natural process that has been optimized during evolution to harness solar energy efficiently and safely, and finally to use it to produce a carbon-based fuel. Initially, solar energy is captured by the light harvesting pigment-protein complexes. In purple bacteria these antenna complexes are constructed on a rather simple modular basis. Light absorbed by these antenna complexes is funnelled downhill to reaction centres, where light drives a trans-membrane redox reaction. The light harvesting proteins not only provide the scaffolding that correctly positions the bacteriochlorophyll a and carotenoid pigments for optimal energy transfer but also creates an environment that can modulate the wavelength at which different bacteriochlorophyll molecules absorb light thereby creating the energy funnel. How these proteins can modulate the absorption spectra of the bacteriochlorophylls will be discussed in this review.

ELECTRO-DEGRADATION OF REACTIVE BLUE DYES USING CYLINDER MODIFIED ELECTRODE: Ti/β-PbO2 AS DIMENSIONALLY STABLE ANODE Aris Mukimin; Karna Wijaya; Agus Kuncaka
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

A cylinder modified electrode of the β-PbO2 was fabricated by anodic electro-deposition method on titanium substrate. The PbO2 layer prepared from high acid solution (pH: 0.3) that contains a mixed of 0.5 M Pb(NO3)2, 1 M HNO3, and 0,02 M NaF. The physicochemical properties of the PbO2 electrode were analyzed by using Energy Dispersive X-Ray Analysis and X-Ray Diffraction. The analyses have shown that oxide layer has an O/Pb ratio about 1.6 and the PbO impurities are formed in the surface layer besides the β-PbO2. The modified electrode was used as anode paired stainless cathode in the electro-degradation of reactive blue dye. The results of the electro-catalytic oxidation process of the dye solution were expressed in terms of the remaining intensity dye and chemical oxygen demand (COD) values. The modified electrode has removal efficiency of the reactive blue dye at voltage of 7 V, pH of 7, concentration NaCl of 2 g/L, initial dye concentration of 100 mg/L with simple and short time operations.

SYNTHESIS, CHARACTERIZATION AND APPLICATION OF DIATOMACEOUS EARTH – 4,4-DIAMINODIPHENYLETHER-O-HYDROXYBENZALDEHYDE AS AN ADSORBENT OF Ag(I) METAL ION Ahmad Fatoni; Soerja Koesnarpadi; Nurlisa Hidayati
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

Synthesis, characterization and application of Diatomaceous Earth-4,4-Diamino diphenylether-O-Hydroxybenzaldehyde (diatomaceous earth-DDE-O-Hb) as an adsorbent of Ag(I) metal ion has been done. The aim of the purification of natural diatomaceous earth with KMnO4, H2SO4 and HCl were to obtain pure diatomaceous earth, remove the other compounds and de-alumination, respectively. The adsorbent of diatomaceous earth-DDE-O-Hb was synthesized by reacting pure diatomaceous earth with 3-chloropropyltrimethoxysilane, 4,4-diaminodiphenylether (DDE) and O-hydroxybenzaldehyde (O-Hb). The FTIR spectroscopy was used to identify Schiff base group in diatomaceous earth-DDE-O-Hb adsorbent. The diatomaceous earth-DDE-O-Hb was applied as adsorbent in the adsorption of Ag(I) metal ion. Parameters influencing the interaction such as time, pH and concentration were optimized. The result showed that diatomaceous earth-DDE-O-Hb adsorbent have Schiff base group. The interaction time of 90 min showed that 70.79% of Ag(I) metal ions at the concentration of 100 ppm can be adsorbed by diatomaceous earth-DDE-O-Hb adsorbent. At the pH solution between 2 to 7, the concentration of 100 ppm of Ag(I) metal ion that can adsorbed by diatomaceous earth-DDE-O-Hb adsorbent was up to 98% and at the concentration of 25 ppm Ag(I) metal ion, the adsorption of Ag(I) by diatomaceous earth-DDE-O-Hb adsorbent was near 91%.

PREPARATION OF HIGHLY ACTIVE Co-Mo/Al2O3 HDS CATALYSTS WITH CITRIC ACID ADDITION BY THE POST-TREATMENT METHOD Nino Rinaldi
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

A study of the influence of citric acid (CA) addition by a post-treatment method during the preparation of a series of Mo/Al2O3 catalysts on the thiophene HDS activity was conducted. The Mo/Al2O3 catalysts were also prepared by a chemical vapor deposition (CVD) technique using Co(CO)3NO to introduce Co atom and characterized by means of NO adsorption, XRD, Mo K-edge EXAFS and XRF. With 8.7 wt% Mo, citric acid was not affected very much for the Co-Mo/Al2O3 catalysts. On the other hand, an outstanding result was shown that the HDS activity was drastically enhanced by 5 times up to Mo content around of 25 wt% Mo. It is suggested that the post treatment increased the dispersion of MoS2 particles, in particular at a high Mo loading. This was also supported by the amount of NO adsorption and amount of Co anchored by the CVD results, which enhanced as the increasing Mo loading up to 25 wt% Mo. Moreover, Mo-CA complex species were observed on the post-treatment method and CVD technique was one of advanced method to prepare Co-Mo-S phases selectively.

THE EFFECT OF PHOSPHORUS ADDITION ON THE ACTIVITY OF BISMUTH MOLYBDATE CATALYST FOR PARTIAL OXIDATION OF PROPYLENE TO ACROLEIN Hamzah Fansuri; Gia Hung Pham; Sandra Wibawanta; Dong-ke Zhang
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

In order to examine the effect of phosphorus addition on the activity and selectivity of bismuth molybdate catalysts for partial oxidation of propylene to acrolein, three modes of phosphorus addition were performed. The three modes of Preparation were performed by (1) adding phosphorus into a-Bi2Mo3O12 to obtain Bi2PxMo3Oy, (2) inserting phosphorus on bismuth sites to obtain Bi2-xPxMo3Oy, and (3) inserting phosphorus on molybdenum sites to obtain Bi2PxMo3-xOy. Four major phases of bismuth phosphomolybdate were detected as the result of the phosphorus addition, namely a-Bi2Mo3O12, Bi9PMo12O52, MoO3, and BiPO4. Experimental results showed that the catalysts solely containing BiPO4 and/or MoO3 have very low activities for partial oxidation of propylene to acrolein. Meanwhile, catalysts containing a-Bi2Mo3O12 and Bi9PMo12O52, together with either MoO3 or BiPO4 showed on average the same activities as a-Bi2Mo3O12 and one of them (combination of a-Bi2Mo3O12, Bi9PMo12O52 and MoO3) has better performance than a-Bi2Mo3O12 at lower temperatures. The presence of the oxygen donor phase, i.e. BiPO4 and MoO3, are believed to play a key role for the high activities of bismuth-phosphomolybdate catalysts. However, at higher temperatures, the presence of oxygen donor reduces the catalyst selectivity to acrolein.

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