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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 1,981 Documents

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SYNTHESIS OF AZO COMPOUNDS DERIVATIVE FROM EUGENOL AND ITS APPLICATION AS A TITRATION INDICATOR Bambang Purwono; Catur Mahardiani
Indonesian Journal of Chemistry Vol 9, No 1 (2009)
Publisher : Universitas Gadjah Mada

The synthesis of azo compounds from eugenol has been carried out by diazotation reaction. The diazonium salt was produced by reaction of aniline and sodium nitrite in acid condition at 0-5 °C temperature to yield benzenediazonium chloride salt. The salt was then reacted with eugenol to produce the azo derivatives. The azo product was analyzed by IR, 1H-NMR, dan GC-MS spectrometer. The results showed that the reaction of benzenediazonium chloride with eugenol gave 4-allyl-2-methoxy-6-hydroxyazobenzene in 34.27% yield for 30 minutes reaction. The derivative of azo compound was dissolved in ethanol and then the color changing was observed in range of pH 9.8-11.1 from yellow to red. Application for titration indicator for acetic acid titrated with sodium hydroxide showed error less than 3.20% compared with phenol phtaline indicator.

A STUDY ON INTERACTION OF Cd(II) AND DIATOMACEOUS EARTH IN ADSORPTION PROCESS Nuryono Nuryono; Suyanta Suyanta
Indonesian Journal of Chemistry Vol 4, No 2 (2004)
Publisher : Universitas Gadjah Mada

In this research, interaction occurring in adsorption process between Cd(II) and active site of diatomaceous earth has been studied. The study was carried out by evaluating Cd(II) adsorption on diatomaceous earth at various pHs, either for the earths without treatment, those after being heated or those treated with sulfuric acid and hydrogen chloride. Adsorption was performed by mixing diatomaceous earth, without and with treatments, and Cd(II) solution for one hour at various pHs (2 - 7), and un-adsorbed metallic ion was analyzed by atomic absorption spectroscopy (AAS). The treatments of diatomaceous earth included heating at temperatures of 300, 500, and 900oC for four hours, treatments with acids (3, 8, and 12 M of H2SO4, and 3, 15, and 18 M of HCl solutions for two hours at 150-200oC). Results showed that the increasing of pH from 2.0 to 3.0 and from 6.0 to 7.0 inclined adsorption of Cd(II) from 13.2 to 23.3 mg/g and from 24.0 to 26.4 mg/g, respectively. At a pH range of 3.0 - 6.0 the adsorption slightly increase from 23.3 to 24.0 mg/g. Heating of diatomaceous earth higher than 500oC caused the adsorption capability to be independence of the pH of solution. On the other hand, treatments with acids (H2SO4 and HCl) caused adsorption capability increased significantly with the increase in pH from 3.0 to 6.0. Adsorption evaluation at the pH range investigated showed that adsorption of Cd(II) on diatomaceous earth may be through interaction between Cd2+ and functional groups of T-OH (T = Si/Al).

ADSORPTION THERMODYNAMICS OF Cd(II), Ni(II), AND Mg(II) ON 3-MERCAPTO-1,2,4-TRIAZOLE IMMOBILIZED SILICA GEL Fahmiati Fahmiati; Nuryono Nuryono; Narsito Narsito
Indonesian Journal of Chemistry Vol 6, No 1 (2006)
Publisher : Universitas Gadjah Mada

Thermodynamics study of Cd(II), Ni(II), and Mg(II) adsorption on silica gel immobilized with 3-mercapto-1,2,4-triazole (SG-SH) has been carried out. Three thermodynamic parameters namely adsorption capacity, equilibrium constant and adsorption energy were determined using model of Langmuir adsorption isotherm. Process of adsorption was carried out by mixing metal ion solution in various concentrations (5 - 400 mg/L) with adsorbent in a batch system. The un-adsorbed ions were determined by Atomic Absorption Spectrophotometry (AAS) and the adsorbed ions were differences of ion concentration in solution before and after adsorption process. Parameters of thermodynamics i.e. capacity (a), equilibrium constant (K) and adsorption energy were determined by using the correlation curve of ratio of equilibrium concentration to the amount of adsorbed metal ions versus equilibrium concentration. Results showed that adsorption of metal ions Ni(II), Cd(II) and Mg(II) on adsorbent of silica gel immobilized with mercapto groups tend to follow Type I (monolayer) of Brunauer's classification. Evaluation of thermodynamic adsorption showed that the order of adsorption capacity was Ni(II) < Cd(II) < Mg(II) with relatively low energy adsorption, in a range of 12 - 18 kJ/mole.

NOVEL DESIGN OF CALANONE DERIVATIVES AS ANTI-LEUKEMIA COMPOUNDS BASED ON QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIP ANALYSIS Ponco Iswanto; Mochammad Chasani; Harjono Harjono; Iqmal Tahir; Muhammad Hanafi; Eva Vaulina YD
Indonesian Journal of Chemistry Vol 11, No 1 (2011)
Publisher : Universitas Gadjah Mada

Leukemia drug discovery based on calanone compound was conducted in previous research and produced 6 calanone derivatives. Most of them have lower activities against leukemia cell L1210 than pure calanone. A Quantitative Structure-Activity Relationship (QSAR) analysis is conducted in this work to find more active calanone derivatives. Six compounds were used as the material of the research because they already have anti-leukemia activity data expressed in Inhibitory Concentration of Fifty Percent Cell Lethal (IC50, in mg/mL). Calculation of predictors was performed by AM1 semiempirical method. QSAR equation is determined using Principle Component Regression (PCR) analysis, with Log IC50 as dependent variable. Independent variables (predictors) are atomic net charges, dipole moment (m), and coefficient partition of n-octanol/water (Log P). This work recommends 3 novel designs of calanone derivatives that may have higher activities (in mg/mL) than those already available, i.e. gemdiol calanone (57.78), 2,4-dinitrophenylhydrazone calanone (30.94) and 2,4,6-trinitrophenylhydrazone calanone (18.96).

ANTI DIABETIC FLAVANONE COMPOUND FROM THE LEAVES OF Artocarpus communis Puspa D.N. Lotulung; Sofa Fajriah; Andini Sundowo; Euis Filaila
Indonesian Journal of Chemistry Vol 9, No 3 (2009)
Publisher : Universitas Gadjah Mada

The Flavanone compound with anti diabetic activity was isolated from ethyl acetate extract of Artocarpus communis leaves using column chromatography techniques. The structure of the flavanone compound was elucidated on the basic of spectroscopic evidence and comparison to published values. This compound, 8-geranyl-4,5,7-trihydroxyflavone, showed strong anti diabetic activity on α-glucosidase inhibition assay with IC50 18.120 µg mL-1.

STUDY OF THERMAL AND ACID STABILITY OF BENTONITE CLAY Karna Wijaya; Ani Setyo Pratiwi; Sri Sudiono; Emi Nurahmi
Indonesian Journal of Chemistry Vol 2, No 1 (2002)
Publisher : Universitas Gadjah Mada

The thermal and acid stability of the bentonite clays (Na- and Ca-bentonite) have been tested. The thermal stability testing has been carried out by heating 5 gram of the clays for five hours at 200, 300 and 500 °C respectively, meanwhile acid stability testing was performed by immersing 5 gram clays into 100 mL sulphuric acid 1M, 2M and 3M for 24 hours. The tested clays, then were characterized by means of X-Ray difractometry and IR-spectroscopy methods. The characterization results showed that upon heating, both Ca- and Na-bentonites indicated same thermal stability. However, upon acid treatment, Na-bentonite was found relatively stabiler and more resistance then Ca-bentonite.

FOUR-FACTOR RESPONSE SURFACE OPTIMIZATION OF THE ENZYMATIC SYNTHESIS OF WAX ESTER FROM PALM KERNEL OIL Erin Ryantin Gunawan; Dedy Suhendra
Indonesian Journal of Chemistry Vol 8, No 1 (2008)
Publisher : Universitas Gadjah Mada

The synthesis of wax ester using refined, bleached and deodorized (RBD) palm kernel oil (PKO) and oley alcohol catalyzed by Lipozyme IM was carried out. Response surface methodology (RSM) based on a five-level, four-factor central composite rotatable design (CCRD) was used to evaluate the interactive effects of synthesis, of reaction time (5-20 h), temperature (20-50 oC), amount of enzyme (0.1-0.2 g) and substrate molar ratio (palm kernel oil to oleyl alcohol, 1:1-1:5) on the percentage yield of wax esters. The optimum condition conditions derived via RSM were reaction time 8.46 h, temperature 44.4 oC, amount of enzyme 0.182 g, substrate molar ratio 1 to 3.7. The actual experimental yield was 92.9 % under optimum condition, which good accordance to the maximum predicted value of 92.4 %.

CHARACTERIZATION OF SURFACE OF THE (010) FACE OF BORAX CRYSTALS USING EX SITU ATOMIC FORCE MICROSCOPY (AFM): Suharso Suharso
Indonesian Journal of Chemistry Vol 5, No 3 (2005)
Publisher : Universitas Gadjah Mada

The surface topology of borax crystals grown at a relative supersaturation of 0.21 has been investigated using ex situ atomic force microscopy (AFM). It was found that the cleavage of borax crystals along the (010) face planes has features of the cleavage of layered compounds, exhibiting cleavage steps of low heights. The step heights of the cleavage of the (010) face of borax crystal are from one unit cell to three unit cells of this face.

PRE-CONCENTRATION AND DETERMINATION OF HEAVY METALS ON MODIFIED ACTIVATED CARBON IN REAL SAMPLES F. Ahmadi; K. Niknam; A. Khanmohammadi; Z. Adibmehr
Indonesian Journal of Chemistry Vol 8, No 2 (2008)
Publisher : Universitas Gadjah Mada

A sensitive and simple method for the simultaneous pre-concentration of nutritionally important minerals in real samples has been reported. The method is based on the formation of metal complexes by N, N'-diacetyl-4-bromo-2, 6-di (aminomethyl) phenol (DBDP) loaded on activated carbon. The metals content on the complexes are then eluted using 6mL 4M HNO3, which are detected by AAS at resonance line. In this procedure, minerals such as Ni, Cu, Co, Pb Zn and Cd can be analyzed in one run by caring out the simultaneous separation and quantification of them. At optimum condition the response are linear over concentration range of for 0.03-1.1 µg mL-1 for Ni2+ , 0.03-1.0 µg mL-1 for Cu2+, 0.02-1.0 µg mL-1 for Pb2+ , 0.02-1.0 µg mL-1 for Co2+,0.02-1.1 µg mL-1 Zn2+ and 0.05-1.3 µg mL-1for Cd2+. The detection limits of each element are expressed as the amount of analytes in µg mL-1 giving a signal to noise ratio of 3 are equal to 2.5, 2.4, 1.6, 2.4, 1.9 and 2.1 for Ni2+ , Cu2+, Pb2+ , Co2+,Zn2+ and Cd2+. The ability of method for repeatable recovery of trace ion are 99.9, 98.7, 99.2 , 98.7, 98.5and 95.6 with R.S.D of 1.3, 1.4, 1.2, 1.4, 1.7 and 1.4 for Ni2+ , Cu2+, Pb2+ , Co2+,Zn2+ and Cd2+. The method has been successfully applied for these metals content evaluation in some real samples including natural water and vegetable.

SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES Komar Sutriah; Zainal Alim Mas’ud; Tun Tedja Irawadi
Indonesian Journal of Chemistry Vol 12, No 2 (2012)
Publisher : Universitas Gadjah Mada

Zinc-difattyalkyldithiocarbamates are organosulfur compounds with many functions, including as an antioxidant in a lubrication system. They were synthesized by reacting secondary fatty amine with ZnCl2 and CS2 giving result zinc-difattyalkyldithiocarbamates of around 77-87%. The synthesized products were characterized using infrared (IR) spectroscopic techniques. The IR spectra of zinc-difattyalkyldithiocarbamates showed sharp bands at 1450-1550 cm-1 for thioureida v (C-N), 950-1050 cm-1 for v (C-S), and in the far-red area 300-400 cm-1 for sulfur-metal bond. Products recovery was evaluated by AAS and the purity was analyzed by HPLC. Seven variants of zinc-difattyalkyldithiocarbamates were obtained. Antioxidant activity was evaluated by rancimat test regarding their induction time. At 125 ppm levels all variants showed higher value in each of their induction time as compared to those of butylated hydroxyanisole and butylated hydroxytoluene, commercial antioxidants No.1, and commercial antioxidants no.2. Three variants, i.e. Zn-bis(dilauryl)dithiocarbamate, Zn-bis(laurylpalmityl)dithiocarbamate, and Zn-bis(laurylstearyl)dithiocarbamate had higher values in their induction time than the other variants. The values are 16.67, 26.54, and 16.11 h, respectively.

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