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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 1,956 Documents
A NEW PHENOLIC COMPOUND FROM ACETONE EXTRACT OF LICHEN Usnea flexuosa Tayl. Maulidiyah Maulidiyah; A. Herry Cahyana; Wahyudi Priyono Suwarso
Indonesian Journal of Chemistry Vol 11, No 3 (2011)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (431.909 KB) | DOI: 10.22146/ijc.21395

Abstract

Natural product, 2'-hydroxy-1'-(4-hydroxyl-5-methoxy-2-methyl-phenyl)-ethanon, (1), was isolated from the thalli lichen Usnea flexuosa Tayl. together with the known (-) - usnic acid (2). The structure of compounds 1 and 2 were determined by the spectroscopic studies.
Mg/Al HYDROTALCITE-LIKE SYNTHESIZED FROM BRINE WATER FOR EOSIN YELLOW REMOVAL Eddy Heraldy; Triyono Triyono; Karna Wijaya; Sri Juari Santosa
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 (373.468 KB) | DOI: 10.22146/ijc.21397

Abstract

Attempts to synthesis of Mg/Al HTlc using magnesium from several raw material resources are widely investigated. One of raw material would purpose as source of magnesium to synthesis of Mg/Al HTlc is brine water which is well known as the desalination process wastewater. Mg/Al HTlc are widely investigated for their potential applications in research and industrial processes as adsorbents, anionic exchange, catalysts and /or catalyst precursors for the preparation of inorganic materials and pharmaceutical industry excipients. As adsorbents, Mg/Al HTlc are receiving greater interests in the environmental community due to their high adsorption capacity. However, there is no literature available on the synthesis of Mg/Al HTlc from brine water except from artificial seawater. The objective of this research is to synthesis of Mg/Al HTlc from brine water and its ability tested for eosin yellow (EY) removal. Characterization of the Mg/Al HTlc synthesized was confirmed through X-ray Diffraction and FT-IR Spectroscopy. The effect of various experimental parameters was investigated using a batch adsorption technique. In this manner, the adsorption isotherms, adsorption kinetics, and pH effects upon EY adsorption on Mg/Al HTlc were examined. The result showed that EY data fit well with the pseudo-second order kinetic model. The isothermal data could be well described by the Freundlich equation. The adsorption capacity was 2.41 × 10-1 mol g-1, and adsorption energy of EY was 24.89 kJ mol-1.
HYDROTHERMAL SYNTHESIS OF ROD AND CHRYSANTHEMUM LIKE NANOSTRUCTURED ZnO Anissa A. Putri; Tutik D. Wahyuningsih; Indriana Kartini
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 (346.418 KB) | DOI: 10.22146/ijc.21399

Abstract

Rod and chrysanthemum-like nanostructured ZnO thin film have been prepared hydrothermally in NaOH and NH3 solution utilizing zinc nitrate hexahydrate as the precursor. ZnO thin films were grown on ITO glass substrate with the seed layer of zinc oxide. Perpendicularly aligned arrays of corrugated ZnO nanorods were grown in NaOH solution, while the chrysanthemum like structure was obtained in ammonia solution. X-Ray diffraction patterns confirmed that both morphologies presenting wurtzite crystal of ZnO. The nanorod showed strong (002) orientation of ZnO.
SYNTHESIS 7-HYDROXY-3’,4’-DIMETHOXYISOFLAVON FROM EUGENOL Andi Hairil Alimuddin; Muhammad Idham Darussalam Mardjan; Sabirin Matsjeh; Chairil Anwar; Mustofa Mustofa; Eti Nurwening Sholikhah
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 (233.66 KB) | DOI: 10.22146/ijc.21404

Abstract

Eugenol from the isolation of clove leaves oil had been utilized in the synthesis of 7-hydroxy-3',4'-dimethoxy-isoflavone based on deoxybenzoin intermediate. The raw material was firstly converted into methyleugenol using DMS (89.87%). Secondly, methyl eugenol was oxidized using KMnO4 to produce 3,4-dimethoxybenzyl carboxylic acid (21%). Friedel-Craft acylation of it with recorcinol produced 3,4-dimethoxybenzyl-2',4'-dihydroxyphenyl ketone (deoxybenzoin intermediate) in 78% yield. Eventually, cyclization of the intermediate with reagents of BF3.OEt2/DMF/POCl3 yielded 7-hydroxy-3',4'-isoflavone in 85% yield.
SYNTHESIS, CHARACTERIZATION AND ADSORPTION TEST OF POLY-TETRA-p-PROPENYLTETRAHYDROXYCALIX[4]ARENE FOR CADMIUM ION Triana Kusumaningsih; Jumina Jumina; Dwi Siswanta; Mustofa Mustofa; Keisuke Ohto; Hidetaka Kawakita
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 (298.647 KB) | DOI: 10.22146/ijc.21408

Abstract

Synthesis, characterization and adsorption test of poly-tetra-p-propenyl-tetrahydroxycalix[4]arene for cadmium ion had been done. The synthesis was carried out in five steps, which were (1) synthesis of p-t-butylcalix[4]arene from p-t-butylphenol, (2) debutylation of p-t-butylcalix[4]arene, (3) tetraallylation of 25, 26, 27, 28 tetrahydroxycalix[4]arene with NaH and allylbromide in dry tetrahydrofuran, (4) Claissen rearrangement of 25, 26, 27, 28-tetrapropenyloxy- calix[4]arene, and (5) polymerization of tetra-p-propenyltetrahydroxycalix[4]arene to yield poly-tetra-p-propenyltetrahydroxycalix[4]arene. Analysis of products was performed using melting point analysis, FT-IR, and 1H NMR spectrometers. The yield of polymerization was 80.35% and m.p > 380 °C. Characterization of poly-tetra-p-propenyltetrahydroxycalix[4]arene was done using SEM and SAA. Structure of poly-tetra-p-propenyltetrahydroxycalix[4]arene was sparsely porous with crosslinked netty architectures, and possessed surface area of 46.572 m2/g. The application of poly-tetra-p-propenyltetrahydroxycalix[4]arene in the adsorption of Cd(II) cation had also been conducted. Adsorption parameters investigated included medium pH and contact time as well as adsorption isotherm. The resin could be applied as a good adsorbent in the adsorption of Cd(II) metal cation. The adsorption followed Langmuir isotherm model, where the measured adsorption capacity, adsorption constant (K), and adsorption energy were 8.5933 x 10-2 mmol/g, 485 L/mmol, and 32.653 KJ/mol, respectively.
IRON CHELATING AND ANTIRADICAL ACTIVITY OF KAYU MANIK LEAVES (Trema orientalis) Salprima Yudha S.; Eka Angasa; Sri Ningsih; Syalfinaf Manaf; Suli Anggria Murni; Fatan Umbara
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 (202.288 KB) | DOI: 10.22146/ijc.21410

Abstract

A methanol soluble fraction extracted from Kayu Manik leaves (Trema orientalis) from Seluma, Bengkulu, exhibited an antiradical activity 69.73% (scavenging activity of the stable 1,1-diphenyl-2-picryl hydrazyl (DPPH) free radical) that was almost similar to that of 1 mM ascorbic acid. On the other hand, the iron chelating activity was 40.74%. We believe that it would be useful to take the results as an alternative for processing industries and can be observed as a good source of new agent for iron chelator.
DETERMINATION OF CONSECUTIVE REACTION RATE CONSTANTS BETWEEN GLYCINE AND ISOLEUCINE WITH o-PHTHALDIALDEHYDE AND 2-MERCAPTOETHANOL FROM SINGLE EXPERIMENT DATA Iip Izul Falah; Triyono Triyono; Catur Atmaji
Indonesian Journal of Chemistry Vol 11, No 1 (2011)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (369.862 KB) | DOI: 10.22146/ijc.21414

Abstract

Kinetics study of chemical reaction is important in producing optimum product, designing a reactor, analyzing a compound, and many other purposes. This work presents the result of study of consecutive pseudo first order reaction between glycine and isoleucine with o-phthaldialdehyde and 2-mercaptoethanol in borate buffer solution at pH=9.0. Continuous detection was used to follow the change of fluorescence intensity of formed isoindole during the reaction. Although concentrations of initial compound and its derivative were not known; by using iteration method, the reaction constants could be determined with high precision from single experiment data. Result of the work showed that reaction rate constants k1 and k2 for consecutive reaction of glycine with excess of o-phthaldialdehyde and 2-mercaptoethanol were 18.75x10-3 and 26.70x10-5 s-1, respectively; whereas for isoleucine were 6.06x10-3 and 12.59x10-5 s-1, respectively.
SYNTHESIS OF POLYPROPYLCALIX[6]ARENE FROM p-t-BUTYLPHENOL AS ADSORBENT FOR Cr(III) METAL ION Susy Yunita Prabawati; Jumina Jumina; Sri Juari Santosa; Mustofa Mustofa
Indonesian Journal of Chemistry Vol 11, No 1 (2011)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (294.13 KB) | DOI: 10.22146/ijc.21417

Abstract

A study has been conducted to synthesize a novel polypropylcalix[6]arene polymer using p-t-butylphenol as a starting material. It was of interest to investigate the capability of the polymer with a tunnel-like structure, as adsorbent to trap the heavy metal cation such as Cr3+. The synthesis was carried out in several steps i.e (1) formation of p-t-butylcalix[6]arene from p-t-butylphenol as a starting material, (2) treatment of p-t-butylcalix[6]arene with 4.95 equivalents of allyl bromide under  alkaline conditions to yield p-t-butyl-37,40-diallyloxy-38,39,41,42-tetra-hydroxy-calix[6]arene, and (3) polymerization of p-t-butyl-37,40-diallyloxy-38,39,41,42-tetrahydroxycalix[6]arene by treatment with concentrated sulfuric acid to yield polypropyl-calix[6]arene. The application of polypropylcalix[6]arene for trapping Cr(III) was investigated by stirring the suspension of calixarene under variation of pH, time, and adsorbent mass. IR and 1H NMR spectra, showed that two allyl groups had been incorporated to the lower rim of the p-t-butylcalix[6]arene and the polymer was obtained as brownish green crystals with the melting point of 108-110 °C. The study also showed that the polypropylcalix[6]arene was able to trap Cr(III) cation. The optimum adsorption conditions were achieved at pH 5, contact time 60 min and concentration 12 mg/l for every 0,008 g of polymer.
PHOSPHOLIPIDS FROM PUMPKIN (Cucurbita moschata (Duch.) Poir) SEED KERNEL OIL AND THEIR FATTY ACID COMPOSITION Tri Joko Raharjo; Laily Nurliana; Sabirin Mastjeh
Indonesian Journal of Chemistry Vol 11, No 1 (2011)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (351.049 KB) | DOI: 10.22146/ijc.21419

Abstract

The phospholipids (PL) of pumpkin (Cucurbita moschata (Duch) Poir) seed kernel and their fatty acid composition were investigated. The crude oil was obtained by maceration with isopropanol followed by steps of extraction yielded polar lipids. The quantitative determination of PLs content of the dried pumpkin seed kernel and their polar lipids were calculated based on the elemental phosphorus (P) contents which was determined by means of spectrophotometric methods. PL classes were separated from polar lipids via column chromatography. The fatty acid composition of individual PL was identified by gas chromatography-mass spectrometry (GC-MS). The total of PL in the pumpkin seed kernels was 1.27% which consisted of phosphatidylcholine (PC), phosphatidylserine (PS) and phosphatidyletanolamine (PE). The predominant fatty acids of PL were oleic and palmitic acid in PC and PE while PS's fatty acid were dominantly consisted of oleic acid and linoleic acid.
CRYSTALLINE PHASE REACTIVITY IN THE SYNTHESIS OF FLY ASH-BASED GEOPOLYMER Lukman Atmaja; Hamzah Fansuri; Anggaria Maharani
Indonesian Journal of Chemistry Vol 11, No 1 (2011)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (710.099 KB) | DOI: 10.22146/ijc.21426

Abstract

Aluminosilicate, alkaline solution and fly ash from a power plant have been used to synthesize geopolymer at ambient temperature. SiO2/Al2O3 mole ratio of the starting materials was varied by the addition of pure, insoluble corundum and quartz. The geopolymer exhibited some differences in the ratio of initial reaction mixtures and that of final products. The corundum gave no influence to the compressive strength while the quartz at SiO2/Al2O3=4.0-6.0 produced significant change in the strength. The highest compressive strength achieved was 65 MPa. XRD using analysis Rietveld method proved that quartz has been found both in starting materials as well as in the geopolymer indicating the involvement of crystalline phases, to some extent, in geopolymerization process.

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