cover
Contact Name
-
Contact Email
-
Phone
-
Journal Mail Official
-
Editorial Address
-
Location
Kab. sleman,
Daerah istimewa yogyakarta
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
THEORETICAL STUDY ON 15-CROWN-5 COMPLEX WITH SOME METAL CATIONS Yahmin Yahmin; Harno Dwi Pranowo; Ria Armunanto
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 (519.918 KB) | DOI: 10.22146/ijc.21353

Abstract

The capability of 15-crown-5 ethers to form complexes with some metal cations (Li+, Na+, K+, Zn2+, Cd2+ and Hg2+) was investigated by an ab initio quantum mechanical method. The calculations were performed at the RHF/lanl2mb level of theory. The interaction energies were used to evaluate the metal binding capability of the crown ether. The effect of nature of the metal on the binding properties was also studied. The results of the calculations showed that the interaction energy of the complexes increased in proportion with the ratio of ion charge, electronegativity and ionization potential to the cation diameter. In addition, based on the extraction distribution coefficient in the gas phase, it is found that the 15-crown-5 could not extract metal cations investigated.
ESTIMATION OF MEASUREMENT UNCERTAINTY IN THE DETERMINATION OF Fe CONTENT IN POWDERED TONIC FOOD DRINK USING GRAPHITE FURNACE ATOMIC ABSORPTION SPECTROMETRY Harry Budiman; Fransiska Sri H; Krismastuti Krismastuti; Nuryatini Nuryatini
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 (310.937 KB) | DOI: 10.22146/ijc.21538

Abstract

The evaluation of uncertainty measurement in the determination of Fe content in powdered tonic food drink using graphite furnace atomic absorption spectrometry was carried out. The specification of measurand, source of uncertainty, standard uncertainty, combined uncertainty and expanded uncertainty from this measurement were evaluated and accounted. The measurement result showed that the Fe content in powdered tonic food drink sample was 569.32 µg/5g, with the expanded uncertainty measurement ± 178.20 µg/5g (coverage factor, k = 2, at confidende level 95%). The calibration curve gave the major contribution to the uncertainty of the final results.
Isolation and Identification of Volatile Components in Tempe by Simultaneous Distillation-Extraction Method by Modified Extraction Method Syahrial Syahrial; M. Muchalal
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 (6976.393 KB) | DOI: 10.22146/ijc.21945

Abstract

An isolation and identification of volatile components in temps for 2, 5 and 8 days fermentation by simultaneous distillation-extraction method was carried out. Simultaneous distillation-extraction apparatus was modified by Muchalal from the basic Likens-Nickerson's design. Steam distillation and benzena as an extraction solvent was used in this system. The isolation was continuously carried out for 3 hours which maximum water temperature In the Liebig condenser was 8 °C. The extract was concentrated by freeze concentration method, and the volatile components were analyzed and identified by combined gas chromatography-mass spectrophotometry (GC-MS). The Muchalal's simultaneous distillation extraction apparatus have some disadvantage in cold finger condenser, and it's extractor did not have condenser. At least 47, 13 and 5 volatile components were found in 2, 5 and 8 days fermentation, respectively. The volatile components in the 2 days fermentation were nonalal, ɑ-pinene, 2,4-decadienal, 5-phenyldecane, 5-phenylundecane, 4-phenylundecane, 5-phenyldodecane, 4-phenyldodecane, 3-phenyldodecane, 2-phenyldodecane, 5-phenyltridecane, and caryophyllene; in the 5 days fermentation were nonalal, caryophyllene, 4-phenylundecane, 5-phenyldodecane, 4-phenyldodecane, 3-phenyldodecane, 2-phenyldodecane; and in the 8 days fermentation were ethenyl butanoic, 2-methy1-3-(methylethenyl)ciclohexyl etanoic and 3,7-dimethyl-5-octenyl etanoic.
QUANTITATIVE RELATIONSHIP OF ELECTRONIC STRUCTURE AND INHIBITION ACTIVITY OF CURCUMIN ANALOGS ON ETHOXYRESORUFIN o-DEALKYLATION (EROD) REACTION Harno Dwi Pranowo; Iqmal Tahir; Ajidarma Widiatmoko
Indonesian Journal of Chemistry Vol 7, No 1 (2007)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (120.597 KB) | DOI: 10.22146/ijc.21717

Abstract

Electronic structure and inhibition activity relationship study of curcumin analogs has been established for 29 curcumin analogs on Ethoxyresorufin O-Dealkylation (EROD) reaction using atomic net charge descriptor based on AM1 semiempirical calculations. The QSAR (Quantitative Structure and Activities Relationships) equation model was determined by statistical parameter from multiple regression analysis and leave-one-out cross validation method. The best QSAR equation was described:log1/IC50 = (36.726±9.028) + (92.368±27.591)qC4 + (260.114±46.029)qC7               + (45.406±9.994)qC10 – (9.287±4.034)qC15 – (8.344±3.685)qC17               – (16.993±3.457)qC18 – (237.490±46.644)qO1 + (293.293±48.749)qO2
INVESTIGATION ON THE MORPHOLOGY AND PROPERTIES OF AGGREGATE STRUCTURES OF NATURAL PHOSPHOLIPIDS IN AQUEOUS SYSTEM USING CRYO-TEM Dwi Hudiyanti; Tri Joko Raharjo; Narsito Narsito; Sri Noegrohati
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 (538.98 KB) | DOI: 10.22146/ijc.21372

Abstract

Cryogenic transmission electron microscopy (Cryo-TEM) was used to investigate the aggregates morphology and properties of candle tree (Aleurites moluccana) endosperm, sesame (Sesamum indicum L. syn.) seeds, and coconut (Cocos nucifera) endosperm phospholipids in dilute aqueous system. The micrographs showed that candle tree phospholipids formed planar bilayer and cluster of vesicles with lipid droplets, while coconut and sesame phospholipids formed well-defined unilamellar vesicles. The vesicles size could be as small as 50 nm in diameter. Coconut phospholipids also showed a good bending ability. Formation of clusters of vesicles was also found in coconut phospholipids dispersion, but this cluster was easily broken by extrusion through a small pore membrane.
DIFFUSION BEHAVIOR OF KETOPROFEN THROUGH CHITOSAN-ALGINATE MEMBRANES Purwantiningsih Sugita; Rini Siswati Asnel; Budi Arifin; Tuti Wukirsari
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (416.425 KB) | DOI: 10.22146/ijc.21429

Abstract

Chitosan-alginate membrane diffusion behavior has been investigated for its application in drugs delivery system. Ketoprofen diffusion behavior assay were performed at 37 and 42 °C to membrane thickness (h) and donor cell concentration of ketoprofen variations (A). The results showed that equilibrium concentrations (Cs) of ketoprofen equation was 27.0087 + 0.09067T - 1.7499h + 0.1030A + 0.0161h2 - 0.0022A2 + 0.0040Th - 0.0018TA + 0.0095hA. The value of Cs was closer to the expected therapy concentration at 50 and 75 mg/L with thin membrane (10-34 μm). Based on Higuchi equation, the model for J and D were J = 11.0849 - 0.2713T - 0.3132h - 0.7461Cs - 0.0096A - 0.0001h2 - 0.0131Cs2 + 0.0002A2 + 0.0084Th + 0.0275TCs - 0.0018TA - 0.0059hCs + 0.0021hA + 0.0037CsA with R2 = 97.9% and D = -12.5000 + 0.2266T + 0.1313h + 0.1538Cs + 0.1200A - 0.0009h2 + 0.0240 Cs2 - 0.0009A2 + 0.0015Th - 0.0150 TCs - 0.0011TA - 0.0096hCs + 0.0004hA + 0.0039CsA with R2 = 98.7%, respectively. The two dimensional contour maps of J versus A and h, both at 37 and 42 °C, showed an increasing of J value as A, h, or T increased.
THE INFLUENCE OF Si/Al MOLE RATIO OF PRECURSOR SOLUTION ON THE STRUCTURAL PROPERTIES OF MCM-41 FROM FLY ASH Sutarno Sutarno; Yateman Arryanto; Stefani Wigati
Indonesian Journal of Chemistry Vol 3, No 2 (2003)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (146.203 KB) | DOI: 10.22146/ijc.21896

Abstract

The synthesis of MCM-41 from fly ash was done hydrothermally at 100°C for 72 hours using supernatant of fly ash solution, sodium silicate, tetramethylammonium hydroxide (TMAOH) and cetyltrimethyl-ammonium hydroxide (CTMAOH) surfactants. The effect of Si/Al mole ratio of precursor solution on the structural properties of MCM-41 was studied by variation of the volume composition of supernatant and sodium silicate. The surfactant was removed by calcination at 550°C for 5 hours with heating rate 2°C/minute. The as-synthesized products were characterized by X-ray diffraction, infrared spectroscopy, and nitrogen adsorption methods. The XRD pattern proved that the samples were MCM-41 and the higher the Si/Al mole ratio of precursor solution resulted MCM-41 with higher crystallinity. Calcination was able to remove the CTMAOH surfactant. It was identified by the disappearance of the peak at 3000-2850 cm-1, which is characteristic for CTMAOH. The XRD pattern of calcined MCM-41 showed the decreaseof dspacing  and the increase of crystallinity. MCM-41 synthesized with Si/Al mole ratio of precursor solution=44.5 showed the highest crystallinity and has specific surface area=694.5 m2/g, average pore diameter=35Å and pore wall thickness=13.6Å.
BIOSORPTION OF METAL IONS Pb(II), Cu(II), AND Cd(II) ON Sargassum duplicatum IMMOBILIZED SILICA GEL MATRIX Buhani Buhani; Suharso Suharso; Zipora Sembiring
Indonesian Journal of Chemistry Vol 6, No 3 (2006)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1252.28 KB) | DOI: 10.22146/ijc.21726

Abstract

Sargassum duplicatum algae biomass is biological material which has a potency to be used as a biosorbent adsorb metal ions from industrial liquid waste, because it has effective functional group as a ligand. However, the ability of the algae biomass in adsorbing of heavy metal ions has some problem such as; tiny size, low density, and easy to be degradated by other microorganism. In addition, algae biomass can not be used directly in adsorption column for its application as the biosorbent. In order to improve physical and chemical prpperties of algae biomass, it needs to be immobilized on silica gel matrix. Series of experiment have been done, morphology analysis of adsorbent surface was performed by using Scanning Electron Microscopy (SEM) and adsorption process to examine the effectiveness of algae biomass immobilized in adsorbing Pb(II), Cu(II), and Cd(II) was performed using batch method at 27 °C. Concentration of metal was determined by using Atomic Absorption Spectrophotometer (AAS) and identification of functional group was conducted using Spectrophotometer Infrared (IR). Data obtained showed that interacting among metal ions with algae biomass is optimum at a range of 60 minutes. Adsorption energies of metal ions resulted from the interaction of metal ions with the functional group of -C=O group from carboxyl and amide on algae biomass and -Si-OH group from silica were at a range of 21.09-25.05 kJ/mole.
IDENTIFICATION OF SOME CARCINOGENIC POLYCYCLIC AROMATIC HYDROCARBONS IN BANGLADESHI VEHICLES EXHAUST TAR BY GAS CHROMATOGRAPHY-MASS SPECTROPHOTOMETER M. Amzad Hossain; S. M. Salehuddin
Indonesian Journal of Chemistry Vol 8, No 3 (2008)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (915.041 KB) | DOI: 10.22146/ijc.21608

Abstract

A more sensitive GC-MS method has been established for the determination of some carcinogenic polycyclic aromatic hydrocarbons (PAHs) in vehicles exhaust tar samples. The tar samples were extracted using dichloromethane (DMC): n-hexane solvent mixture. A multi-layer clean-up (silica gel/sodium sulphate) column was used, followed by glass fiber filter (GFF) paper. The method was successfully applied to determine a number of PAHs present in exhaust tar sample of different vehicles of the Atomic Energy Centre, Dhaka, Bangladesh.
SEPARATION OF PENICILLIN G FROM FERMENTATION BROTH BY EMULSION LIQUID MEMBRANE TECHNIQUE Imam Santoso; Bachri Amran; Apriliana Laily Fitri
Indonesian Journal of Chemistry Vol 10, No 1 (2010)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (239.806 KB) | DOI: 10.22146/ijc.21496

Abstract

The separation of penicillin G from fermentation broth can be done by emulsion liquid membrane technique. The aim of this research is to establish the optimal conditions for the extraction and separation of penicillin G using emulsion liquid membrane technique. The optimal conditions were found to be at ratio of internal phase volume to membrane phase volume of 1:1 ; time of making emulsion, 1 min ; emulsion contact rate, 300 rpm; rate of stirring of emulsion, 2000 rpm ; rest time of emulsion, 13 min; concentration of  penicillin G as external phase, 375 ppm; and concentration of surfactant, 5% (v/v). pH of internal phase is 8; pH of external phase 5; ratio of emulsion phase volume to external phase volume, 1:2 and concentration of carrier 2 mM. The concentration of penicillin G and phenylacetic acid from fermentation results were 24771 mg/L and 32675 mg/L. Extraction by emulsion liquid membrane technique gave the percentage of penicillin G 53.38% and phenylacetic acid 60.41%. The percentage phenylacetic acid which is still higher (60.41%) indicated that the penicillin G could not completely be separated from phenylacetic acid by emulsion liquid membrane technique.

Page 37 of 199 | Total Record : 1981


Filter by Year

2001 2026


Filter By Issues
All Issue Vol 26, No 1 (2026) Vol 25, No 5 (2025) Vol 25, No 4 (2025) Vol 25, No 3 (2025) Vol 25, No 2 (2025) Vol 25, No 1 (2025) Vol 24, No 6 (2024) Vol 24, No 5 (2024) Vol 24, No 4 (2024) Vol 24, No 3 (2024) Vol 24, No 2 (2024) Vol 24, No 1 (2024) Vol 23, No 6 (2023) Vol 23, No 5 (2023) Vol 23, No 4 (2023) Vol 23, No 3 (2023) Vol 23, No 2 (2023) Vol 23, No 1 (2023) Vol 22, No 6 (2022) Vol 22, No 5 (2022) Vol 22, No 4 (2022) Vol 22, No 3 (2022) Vol 22, No 1 (2022) Vol 22, No 2 (2022) Vol 21, No 6 (2021) Vol 21, No 5 (2021) Vol 21, No 4 (2021) Vol 21, No 3 (2021) Vol 21, No 2 (2021) Vol 21, No 1 (2021) Vol 20, No 6 (2020) Vol 20, No 5 (2020) Vol 20, No 4 (2020) Vol 20, No 3 (2020) Vol 20, No 2 (2020) Vol 20, No 1 (2020) Vol 19, No 4 (2019) Vol 19, No 3 (2019) Vol 19, No 2 (2019) Vol 19, No 1 (2019) Vol 18, No 4 (2018) Vol 18, No 3 (2018) Vol 18, No 2 (2018) Vol 18, No 1 (2018) Vol 17, No 3 (2017) Vol 17, No 2 (2017) Vol 17, No 1 (2017) Vol 16, No 3 (2016) Vol 16, No 2 (2016) Vol 16, No 1 (2016) Vol 15, No 3 (2015) Vol 15, No 2 (2015) Vol 15, No 1 (2015) Vol 14, No 3 (2014) Vol 14, No 2 (2014) Vol 14, No 1 (2014) Vol 13, No 3 (2013) Vol 13, No 2 (2013) Vol 13, No 1 (2013) Vol 12, No 3 (2012) Vol 12, No 2 (2012) Vol 12, No 1 (2012) Vol 11, No 3 (2011) Vol 11, No 2 (2011) Vol 11, No 1 (2011) Vol 10, No 3 (2010) Vol 10, No 2 (2010) Vol 10, No 1 (2010) Vol 9, No 3 (2009) Vol 9, No 2 (2009) Vol 9, No 1 (2009) Vol 8, No 3 (2008) Vol 8, No 2 (2008) Vol 8, No 1 (2008) Vol 7, No 3 (2007) Vol 7, No 2 (2007) Vol 7, No 1 (2007) Vol 6, No 3 (2006) Vol 6, No 2 (2006) Vol 6, No 1 (2006) Vol 5, No 3 (2005) Vol 5, No 2 (2005) Vol 5, No 1 (2005) Vol 4, No 3 (2004) Vol 4, No 2 (2004) Vol 4, No 1 (2004) Vol 3, No 3 (2003) Vol 3, No 2 (2003) Vol 3, No 1 (2003) Vol 2, No 3 (2002) Vol 2, No 2 (2002) Vol 2, No 1 (2002) Vol 1, No 3 (2001) Vol 1, No 2 (2001) Vol 1, No 1 (2001) ARTICLE IN PRESS Article in press More Issue