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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 22 Documents

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Search results for , issue "Vol 17, No 2 (2017)" : 22 Documents clear

Synthesis of 1,4-Dioxaspiro[4.4] and 1,4-Dioxaspiro[4.5] Novel Compounds from Oleic Acid as Potential Biolubricant Yehezkiel Steven Kurniawan; Yudha Ramanda; Kevin Thomas; Hendra Hendra; Tutik Dwi Wahyuningsih
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

Two 1,4-dioxaspiro novel compounds which derivated from methyl 9,10-dihydroxyoctadecanoate (MDHO) with cyclopentanone and cyclohexanone had been synthesized by a sonochemical method in the presence of montmorillonite KSF catalyst. The MDHO compound had been prepared from 9,10-dihydroxyoctadecanoic acid (DHOA) and methanol. Meanwhile, DHOA was synthesized by hydroxylation of oleic acid with the solution of 1% KMnO4 under basic condition. The structures of the products were confirmed by FTIR, GC-MS, 1H-NMR, and 13C-NMR spectrometers. Hydroxylation reaction of oleic acid gave DHOA as a white solid powder in 46.52% yield (m.p. 131-132 °C). On the other side, esterification reaction via sonochemical method between DHOA and methanol gave MDHO as a white powder in 93.80% yield (m.p. 80-81 °C). The use of cyclopentanone in 45 min sonochemical method gave methyl 8-(3-octyl-1,4-dioxaspiro[4.4]nonan-2-yl)octanoate as a yellow viscous liquid in 50.51% yield. The other compound, methyl 8-(3-octyl-1,4-dioxaspiro[4.5]decan-2-yl)octanoate as yellow viscous liquid had been synthesized by similar method with cyclohexanone via the sonochemical method in 45.12% yield. From physicochemical properties, i.e. density, total acid number, total base number, and iodine value, gave the conclusion that these novel compounds are potential biolubricant candidates to be developed.

Performance Test of K0-NAA and Relative Method for Analysis of Al, Mg, K Nuclides in SRM Lake Sediment Sample Sunardi Sunardi; Darsono Darsono
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

A performance test has been conducted of k0-NAA and relative methods for analysis of Al, Mg, K nuclides in SRM lake sediment sample (SRM SL-3). The performance test included validation, accuracy and precision tests, as well as t and F test. This test is done in order to know the performance of the both methods. Test results on validation test of both the k0-NAA and relative methods obtained were still in good performance with z-score values within the range of -2 ≤ x ≤ 2, in the accuracy and precision test showed that the two methods used were still reliable or passed the test for elemental analysis. The results of the evaluation t-test were at 95% confidence level showed that both methods were no significant differences in the test results, and the evaluating the F test showed that there are no differences in the accuracy between the two methods. The performance test data are expected to be used by practitioners and users of neutron activation analysis services as the reference option of analysis method to optimize the objectives to be achieved.

The Optimum Conditions of Carboxymethyl Chitosan Synthesis on Drug Delivery Application and Its Release of Kinetics Study Parsaoran Siahaan; Nadira Cahyaning Mentari; Ustera Octovindra Wiedyanto; Dwi Hudiyanti; Suci Zulaikha Hildayani; Marlyn Dian Laksitorini
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

In this paper, carboxymethyl chitosan (CMC) was synthesized and studied as a carrier to encapsulate vitamin (as drug model) and controlled release. Chitosan (CS) is a polycationic derivated from chitin, which suitable for active substance carrier system on biomedical function. CS has good properties such as non-toxic, biodegradable, and biocompatible. However, CS insoluble in an aqueous solvent so CS was modified chemically into CMC. CMC was formed by reacting CS and monochloroacetic acid with sodium hydroxide (NaOH) as a catalyst. Optimation was performed by varying the NaOH concentration during alkalizing the CS and the temperature reaction. The functional group and crystallinity of CS and CMC were estimated by FTIR and XRD. The degree substitution of carboxymethylation has an average value of 0.60. The results show optimum temperature reaction and NaOH concentration were 60 °C and 40% (w/v). The nicotinamide (NA), a hydrophilic vitamin, was loaded within CMC matrix system through in vitro precipitation method. To confirm the encapsulation of NA in CMC and the release kinetics of NA from CMC in distilled water was studied through UV-Vis spectrophotometry. The release profile of NA from CMC matrix system carried out for 3 h and 12 h. The rate of NA release from CMC increases with increasing time and the follows a zero order, Higuchi, and Korsmeyer-Peppas kinetics rules.

Supramolecular Phosphorescent Trinuclear Copper(I) Pyrazolate Complexes for Vapochromic Chemosensors of Ethanol Hendrik Oktendy Lintang; Nur Fatiha Ghazalli; Leny Yuliati
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

We highlight that by using supramolecular single crystals of phosphorescent trinuclear copper(I) pyrazolate complexes with different molecular structures (2A-E), vapochromic chemosensors were successfully designed for sensing ethanol with high sensing capability. These complexes 2A-E were synthesized from non-side chain, 3,5-dimethyl, 3,5-bis(trifluoromethyl), 3,5-diphenyl and 4-(3,5-dimethoxybenzyl)-3,5-dimethyl pyrazole ligands (1A-E) in 83, 97, 99, 88 and 85% yields, respectively. All complexes showed emission bands centered at 553, 584, 570 and 616 nm upon an excitation at 280 nm for complexes 2A-C,E, respectively and 642 nm upon an excitation at 321 nm for complex 2D with lifetime in microseconds, indicating a large Stoke shift for phosphorescent compounds. These emission spectra were in good agreement with their colors from green to red upon exposure to a UV lamp with an excitation at 254 nm in dark room. Upon exposure to ethanol in 5 min, quenching, photoinduced energy transfer and shifting of emission intensities were observed for chemosensors 2A-C, 2D and 2E, respectively. Interestingly, chemosensor 2E only showed completely and autonomously recovery of its original emission intensity. Such novel finding in sensing capability might be caused by a weak intermolecular hydrogen bonding interaction of ethanol to oxygen atoms at dimethoxybenzyl side-chains of the pyrazole ring.

Production of Biodiesel from Seed Oil of Nyamplung (Calophyllum inophyllum) by Al-MCM-41 and Its Performance in Diesel Engine Hendro Juwono; Triyono Triyono; Sutarno Sutarno; Endang Tri Wahyuni; Ita Ulfin; Fredy Kurniawan
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

Production of biodiesel from crude nyamplung oil (Calophyllum inophyllum) have been done by transesterification using Al-MCM-41 catalyst. Al-MCM-41 catalyst was obtained from impregnation of MCM-41 by Al. Sodium aluminate was added to MCM-41 until pH 11.5. The mixture was heated until 110 °C for 5 days. The calcination was performed at 500 °C, and then cooled at room temperature. The Al-MCM-41 obtained was characterized using SAXRD. Morphology of the surface was analyzed using SEM. The metals content were measured using XPS. Performance of Al-MCM-41 to adsorp and desorp nitrogen was also monitored by GSA using BET model. Acidity of the Al-MCM-41 was analyzed by FTIR using absorption of pyridine. The catalytic activity was measured using gas chromatography-mass spectrometry (GC-MS). The chromatogram shows that conversion Nyamplung seed oil to biodiesel is 98.15%. The performance of biodiesel obtained was analyzed by use it to diesel engine. The biodiesel obtained was mixed with commercial diesel fuel in various volume ratios (i.e. 0, 10, 20, 30 and 100%) before used. Viscosity, flash point, boiling point, cloud point, and pour point of the mixtures were characterized. These measuring properties increase with the increase of biodiesel concentration. Optimum engine power was achieved by 10% biodiesel. The mixture of 10% biodiesel has similar characteristic to commercial diesel fuel at load until 1800 watt.

Comparison of NAA XRF and ICP-OES Methods on Analysis of Heavy Metals in Coals and Combustion Residues Agus Taftazani; Roto Roto; Novitasari Restu Ananda; Sri Murniasih
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

Heavy metals in the samples of coals and combustion residues (bottom ash and fly ash) from Pacitan coal-fired power plant (CPP) have been identified by using NAA, XRF, and ICP-OES methods. This research was aimed to understand the analysis results correlation coefficient (R) and determine the enrichment ratio (ER) value of the samples by using three analysis methods. The results showed 10 elements have been simultaneously detected in all samples. The correlation coefficient of analysis results of metals content in coals by using NAA-XRF, XRF-ICP OES and with ICPOES-NAA methods gives R2£1 respectively. The correlation coefficient of analysis results of metals content in bottom ash and fly ash by using the methods of NAA-XRF, XRF-ICPOES, and ICPOES-NAA gained R2»1 respectively. ICP-OES method was most satisfactory in this study. The value of ER for identified metals by using the three methods in the samples of bottom ash and fly ash yielded the value over one, and ER value of fly ash was greater in comparison to the bottom ash.

Cobalt Oxide-Modified Titanium Dioxide Nanoparticle Photocatalyst for Degradation of 2,4-Dichlorophenoxyacetic Acid Leny Yuliati; Nur Azmina Roslan; Wai Ruu Siah; Hendrik Oktendy Lintang
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

2,4-dichlorophenoxyacetic acid (2,4-D) has been recognized as a possibly carcinogenic compound to human, therefore, 2,4-D should be treated before it is discharged to the environment. Photocatalytic degradation of 2,4-D has been proposed as one of the best methods that offer environmentally safe process. In the present research, titanium dioxide (TiO2) was modified with cobalt oxide (CoO) and tested for photocatalytic degradation of 2,4-D under UV light irradiation. Different amounts of CoO (0.1, 0.5, 1 and 5 mol%) were added onto TiO2 by an impregnation method. The photocatalytic reaction was monitored and analyzed by measurement of 2,4-D absorbance using UV spectrophotometer. After 1 h photocatalytic reaction, it was confirmed that the sample with low loading of 0.1 mol% gave the highest photocatalytic activity among the bare and modified TiO2 photocatalysts. The photocatalytic activity was decreased with the increase of CoO loading, suggesting that the optimum amount of CoO was an important factor to improve the performance of TiO2. Based on fluorescence spectroscopy, such addition of CoO resulted in the reduced emission intensity, which showed the successful decrease in the electron-hole recombination.

Effect of Anodizing Time and Annealing Temperature on Photoelectrochemical Properties of Anodized TiO2 Nanotube for Corrosion Prevention Application Misriyani Misriyani; Abdul Wahid Wahab; Paulina Taba; Jarnuzi Gunlazuardi
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

A study on the influence of anodizing time, annealing temperature and photoelectrochemical properties of TiO2 nanotube (TiO2 NT) has been investigated. The crystallinity was investigated using X-Ray Diffraction and the anti-corrosion performance of stainless steel 304 (SS 304) coupled with TiO2 NT was evaluated using electrochemical techniques under ultraviolet exposure. The optimum anodizing condition occurs at a voltage of 20 V for 3 h. After anodizing, the TiO2 NT amorf was calcined at 500 °C to obtain anatase crystalline phase. For the photoelectrochemical property, the effects of pH and NaCl concentration on corrosion prevention have been examined. The result showed that the corrosion rate of stainless steel 304 coupled with TiO2 NT can be reduced up to 1.7 times compared to the uncoupled stainless steel 304 (3.05×10-6 to 1.78×10-6 mpy) under ultraviolet exposure by shifted the photopotential to the more negative value (-0.302 V to -0.354 V) at a pH of 8 and 3% NaCl concentration (-0.264 V to -0.291 V). In conclusion, the TiO2 NT films, which was prepared by anodization and followed by annealing can prevent the corrosion of stainless steel 304.

Microwave-Assisted Organic Reactions: Eco-friendly Synthesis of Dibenzylidenecyclohexanone Derivatives via Crossed Aldol Condensation Sri Handayani; Cornelia Budimarwanti; Winarto Haryadi
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

The synthesis of dibenzylidenecyclohexanone derivatives via environmentally friendly Microwave Assisted Organic Synthesis (MAOS) crossed aldol condensation had been carried out. The condensation reaction to synthesize the dibenzylidenecyclohexanone 8b was performed by reacting benzaldehyde 4 and cyclohexanone 2 (mole ratio of 2:1) with NaOH as catalyst for 2 min under microwave irradiation. The benzaldehyde derivatives used in this study were 4-methoxybenzaldehyde and 3,4-dimethoxybenzaldehyde and gave of (2E,6E)-bis(4-methoxy benzylidene)cyclohexanone 8a and (2E,6E)-bis(3,4-dimethoxybenzylidene)cyclohexanone 8c, respectively. The study was commenced by searching the optimum concentration of NaOH. The reaction yield was determined by TLC scanner and the structure was elucidated by FTIR and NMR spectrometers. For the comparison, the reaction was also carried out by using stirring method. The results showed that optimum concentration of NaOH was 5 mmole. By using the optimum condition via MAOS method, the compounds 8a, 8b and 8c were obtained in 100, 98 and 93%, respectively. The research also proved that the method of dibenzylidenecyclohexanones (8) synthesis using MAOS was more efficient than stirring method.

Coating of L-Arginine Modified Silica on Magnetite through Two Different Sol-Gel Routes Amaria Amaria; Suyanta Suyanta; Nuryono Nuryono
Indonesian Journal of Chemistry Vol 17, No 2 (2017)
Publisher : Universitas Gadjah Mada

In this research, magnetite coated with L-arginine modified silica (Fe3O4/SiO2-GPTMS-Arg) has been synthesized through a sol-gel process at a room temperature in two Routes. In Route 1, a precursor of sodium silicate solution (source of SiO2), 3-glycidoxypropyltrimethoxysilane (GPTMS) as a coupling agent and L-arginine (Arg) as the source of functional groups were added sequentially to magnetite nanoparticles (Fe3O4). Gelling was carried out by adding HCl solution dropwise to the mixture to reach pH of 7.0. The product was washed with water and ethanol and then dried at 65 °C for 1 day. In Route 2, sodium silicate solution was added to a mixture of GPTMS and L-arginine, and then the sol obtained was added into magnetite nanoparticles. The results were characterized with FTIR spectroscopy, X-ray diffraction, atomic absorption spectroscopy and volumetric method to identify functional groups, crystal size, iron ions released and amino groups content, respectively. The results showed that Fe3O4/SiO2-GPTMS-Arg has been successfully synthesized through both two routes. Route 1, however, gave product of Fe3O4/SiO2-GPTMS-Arg more stable and more content of amino groups than Route 2. The presence of amino groups leads to the application of the product for metal ion removal from aqueous solution.

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