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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 1,981 Documents

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PHYTOCHEMICAL STUDY ON THE ETHYLACETATE EXTRACT OF THE LEAVES OF Mesua ferrea LINN S. M. Mizanur Rahman; Swati Shabnom; M. Abdul Quader; M. Amzad Hossain
Indonesian Journal of Chemistry Vol 8, No 2 (2008)
Publisher : Universitas Gadjah Mada

Furano-napthyl-hydroxy cyclohexyl type of compound was isolated first times in plant from the ethyl extracts of the leaves of Mesua ferrea. The structure of the compound has been established by the modern spectroscopic techniques such as UV, IR, 1H-NMR, 13C-NMR and mass spectroscopy and identified as 12, 13-furano-8-hydroxy napthyl-6-0-b-2',3',4',6' tetrahydroxy-5',5' dimethyl cyclohexyl ether.

UTILIZATION OF Penaus monodon SHRIMP SHELL WASTE AS ADSORBENT OF CADMIUM(II) IN WATER MEDIUM Sari Edi Cahyaningrum; Amaria Amaria
Indonesian Journal of Chemistry Vol 5, No 2 (2005)
Publisher : Universitas Gadjah Mada

Utilization of shrimp shell has been optimum so that in this research preparation of adsorbent chitosan from shell of shrimp (Penaus monodon) as raw materials for cadmium(II) adsorption was carried out. The chitin was made by the deproteination, demineralization; chitosan was prepared by chitin deacetylation. This work was started with Infra Red Spectroscopic identification of functional group. Percentage of deacetylation was determined also by Infra Red Spectroscopy. Contant of nitrogen was determined by Kjeldhal method. The isotherm adsorption Langmuir model was employed for the determination of the energy and the capacity in adsorption. Result showed that chitosan could be isolated from shrimp shell waste with % deacetylation degree of 79.80 and % nitrogen 7.11. Cadmium(II) was chemically adsorbed on chitosan involving energi adsorption of 32.27 kJ/mole. Adsorption capacity of cadmium(II) was 6.35 x 10-5 mole/g. The constant adsorption rate k, was 0.91 x 10-3 s-1 and equilibrium adsorption desorption are K = 10.28 x 103. The ability adsorption of chitosan in real waste has the efficiency of 90%.

SYNTHESIS OF THE ISOQUINO-[2,1-c][1,3]-BENZODIAZEPINE DERIVATIVE FROM PAPAVERINE I Made Sudarma; John Bremner
Indonesian Journal of Chemistry Vol 7, No 3 (2007)
Publisher : Universitas Gadjah Mada

The objective of this research was to synthesize isoquino[2,1-c][1,3]benzodiazepine from papaverine alkaloid. Functional Group Interconversion (FGI) and Carbon -Nitrogen bond connection approach was investigated. Papaverine (1) was nitrated by HNO3 to compound (2) and followed by reduction with Sn and HCl to afford aminonorlaudanosine (3). Formation of cyclic benzodiazepine (4) was achieved by reaction of (3) with CS2. Products of reactions were confirmed by Nuclear Magnetic Resonances (n.m.r), Mass Spectrum, and Fourier Transform Infra Red (FTIR).

Kinetics and Mechanism of Ni/Zeolite-Catalyzed Hydrocracking of Palm Oil into Bio-Fuel Sri Kadarwati; Fitri Rahmawati; Puji Eka Rahayu; Kasmadi Imam Supardi
Indonesian Journal of Chemistry Vol 13, No 1 (2013)
Publisher : Universitas Gadjah Mada

Kinetics and mechanisms of Ni/zeolite-catalyzed cracking reaction of methyl ester palm oil (MEPO) were studied using a continuous flow-fixed bed reactor system at an atmospheric pressure. The catalyst was prepared by wet impregnation method with a solution of nickel nitrate hexahydrate as the precursor and zeolite as carrier. The characteristics of catalyst including active Ni metal content, crystallinity, total acidity, and porosity were evaluated. The reactions were performed with a varied hydrogen flow rate as a carrier gas as well as a reductant and reaction time. Liquid products were analyzed by GC. Analysis by GC-MS was only conducted on a product at hydrogen flow rate with the best conversion. It has been shown that the catalyst has a superior character for hydrocracking reactions of MEPO into green fuel. No considerable effect of hydrogen flow rate on the total conversion was observed. The tests showed that the kinetics of Ni/zeolite-catalyzed cracking reaction followed pseudo-first order kinetics. GC-MS analysis revealed the formation of light hydrocarbon products with C6-C8 of aliphatic and cyclic components without oxygenates. Distribution of the product indicated that the cracking reaction as well as the isomerization of the products of hydrocracking occurred. Thus, Ni/zeolite-catalyzed cracking involved cracking /hydrogenation, isomerization, cyclization, and deoxygenation.

MOLECULAR INTERACTION BETWEEN BENZONITRILE AND HEXAMETHYLPHOSPHORIC TRIAMIDE BY 13C NMR T1 RELAXATION TIME STUDIES AND AB INITIO QM CALCULATIONS: EXTENDED INVESTIGATION Parsaoran Siahaan; Cynthia L. Radiman; Susanto Imam Rahayu; Muhamad A. Martoprawiro; Dieter Ziessow
Indonesian Journal of Chemistry Vol 9, No 2 (2009)
Publisher : Universitas Gadjah Mada

It has been obtained the anisotropy ratio a = T1(ortho-,meta-13C)/T1(para-13C) of dilute solutions of bn change from 1.7 in fa solution and 1.5 in neat bn to 1.0 in HMPT. Thus the anisotropy ratio comes out to be a = 1. In HMPT, obviously, solvent molecules cluster around Ph-CºN in such a way, that non-covalent interactions lead to isotropic reorientational motion like a spherical molecule. To conform with the T1 times, a layer arrangement with at least two HMPT molecules per Ph-CºN seems to be likely. From computational quantum calculations of non-covalent intermolecular interactions and Mie potential analysis, the solute-solvent molecular pairs in bnּּּHMPT have almost equal interaction energies for the ortho, meta, and para configuration and the layered configurations are energetically permitted

Preparation of Nickel/Active Carboncatalyst and its Utilization for Benzene Hydrogenation Enggelena Septiawati; Iip Izul Falah; RHA. Sahirul Alim
Indonesian Journal of Chemistry Vol 1, No 2 (2001)
Publisher : Universitas Gadjah Mada

The research on the preparation of nickel catalyst impregnated on active carbon by two methods has been carried out. The impregnation of Ni metal was done using nickel(II) chloride as a precursor. The impregnated of Ni metal on samples in A method was made in varying of percentage i.e., 0.5, 1.0 and 2.0% (w/w) as the weight proportion of Ni to active carbon and NiCl2.6H20. The concentration of Ni that would be impregnated on samples in B method was made close to Ni content of samples in A method determined by atomic adsorption spectrometry. Preparation of nickel/active carbon catalyst with A method was done with dipping the active carbon in the nickel(II) chloride solution followed by filtering and then drying at 110 °C for 4 hours, and then calcination by flowing nitrogen and reduction by hydrogen, each at 400 °C at 4 hours. The treatments made on samples in A method was also done on samples in B method, the only difference was evaporating all of precursor solution after dipping active carbon in that precursor solution was done in B method. The characterization includes: iodium adsorption test, determination of nickel content by means of atomic adsorption spectrometry, and acidity by adsorption of ammonia methods. Test of catalyst activity was done by means of hydrogenation of benzene to cyclohexane at 150, 200 and 250 °C, the pressure of 1 atm and the flow rate of hydrogen 6 mL/minute. The products were analyzed by gas chromatographic method. The results show that A method produced a catalyst with relatively low nickel content. However the acidity and ability to convert benzene to cyclohexane were relatively high and it increased as increasing the content of nickel. The temperature of the reaction was achieved at 250 °C which gave the yield on conversion of 25.3678%. The catalyst obtained by B method in the same condition of hydrogenation gave only smaller results.

SYNERGISTIC EXTRACTION OF COBALT(II) WITH MIXTURE OF ACYL-PYRAZOLON AND CROWN-ETHER IN STRONSIUM(II) ENVIRONMENT Bambang Rusdiarso
Indonesian Journal of Chemistry Vol 7, No 1 (2007)
Publisher : Universitas Gadjah Mada

Synergistic extraction of cobalt(II) with mixture of acyl-pyrazolon (HL) and crown-ether (E) in the Sr(NO3)2 environment has been studied. In this research, HPMBP (phenyl-1-methyl-3-benzoil-4-pyrazolon-5) was used, with three different kinds of crown-ether, i.e. (benzo-15-crown-5), DB18C6 (dibenzo-18-crown-6) and DB24C8 (dibenzo-24-crown-8), in chloroform. In the bulk environment of stronsium, a cobalt coextraction and stronsium occured with species ESrNO3+,Co(PMBP)3-, and E = B15C5, while Co(PMBP)2E and ESr,Co(PMBP3)2, with E = DB18C6. There was no coextraction when using crown-ether DB24C8, with the extracted species Co(PMBP)2E. Values of extraction constant presented in log Kex were -6.08 (B15C5), - 4.51, -12.55 (DB18C6), and - 4.57 (DB24C8), respectively.

SYNTHESIS, CHARACTERIZATION AND ANTIOXIDANT ACTIVITY OF 7-HYDROXY-3',4'-DIMETHOXYFLAVONE Elfi Susanti VH; Sabirin Matsjeh; Tutik Dwi Wahyuningsih; Mustofa Mustofa; Tri Redjeki
Indonesian Journal of Chemistry Vol 12, No 2 (2012)
Publisher : Universitas Gadjah Mada

Synthesis of flavones and their derivatives has attracted considerable attention due to their significant pharmaceutical effects. 7-hydroxy-3',4'-dimethoxyflavone has been synthesized and its antioxidant activity has been investigated. Flavone was synthesized by oxidative cyclization of chalcone. 2',4'-dihydroxy-3,4-dimethoxychalcone was prepared by Claisen-Schmidt condensation of 2,4-dihydroxyacetophenones with 3,4-dimethoxybenzaldehydes in the presence of aqueous solution of sodium hydroxide and ethanol at room temperature. Oxidative cyclization of 2',4'-dihydroxy-3,4-dimethoxychalcone was done by using I2 catalyst in DMSO to form 7-hydroxy-3',4'-dimethoxyflavone. The synthesized compounds were characterized by means of their UV-Vis, IR, 1H-NMR and 13C-NMR spectral data. The compound was tested for their antioxidant activities by DPPH method.

EFFECT OF AGING TIME TOWARD CRYSTALLINITY OF PRODUCTS IN SYNTHESIS OF MESOPOROUS SILICATES MCM-41 Suyanta Suyanta; Narsito Narsito; Endang Tri Wahyuni; Triyono Triyono; Sutarno Sutarno
Indonesian Journal of Chemistry Vol 10, No 3 (2010)
Publisher : Universitas Gadjah Mada

Researches about the effects of aging time toward crystallinity of products in the synthesis of mesoporous silicates MCM-41 have been done. MCM-41 was synthesized by hydrothermal treatment to the mixture of sodium silicate, sodium hydroxide, cetyltrimetylammoniumbromide (CTMAB) and aquadest in the molar ratio of 8Na2SiO3 : CTMAB : NaOH : 400H2O. Hydrothermal treatment was carried out at 110 °C in a teflon-lined stainless steel autoclave heated in the oven, with variation of aging time, i.e.: 4, 8, 12, 16, 24, 36, 48, and 72 h respectively. The solid phase were filtered, then washed with deionised water, and dried in the oven at 100 °C for 2 h. The surfactant CTMAB was removed by calcinations at 550 °C for 10 h with heating rate 2 °C/min. The as-synthesized and calcined powders were characterized by using FTIR spectroscopy and X-ray diffraction method. The relative crystallinity of products was evaluated based on the intensity of d100 peaks. The best product was characterized by using N2 physisorption method in order to determine the specific surface area, mean pore diameter, lattice parameter, and pore walls thickness. It was concluded that the relative crystallinity of the products was sensitively influenced by the aging time. The highest relative crystallinity was achieved when used 36 h of aging time in hydrothermal treatment. In this optimum condition the product has 946.607 m2g-1 of specific surface area, 3.357 nm of mean pore diameter, 4.533 nm of lattice parameter, and 1.176 nm of pore walls thickness.

BIODEGRADATION OF POLYBLEND POLYPROPILENE- PALM OIL-AMYLUM BY Bacillus subtilus AND Clostridium botulinum Zainal Fanani; Miksusanti Miksusanti; Desnelli Desnelli
Indonesian Journal of Chemistry Vol 3, No 3 (2003)
Publisher : Universitas Gadjah Mada

It had been done a biodegradation polyblend from blending polypropilene-palm oil-amylum with three composition of polyblend i.e polyblend A 80% polypropilene- 19.5% palm oil- 0.5% amylum, poliblend B 80% polypropilene- 19% palm oil- 1% amylum and polyblend C 80% polypropilene-18% palm oil- 2% amylum by B. subtilus and C. botulinum, time incubation was twenty five days. The characterization of polyblend before and after biodegradation has done with FTIR, DTA, Viscometre and tensile strength of polyblend. The result showed that Bacillus subtilus and Clostridium botulinum can biodegradate polyblend and make holes as well as chink on polyblend especially polyblend C, because it has more carbohidrat than polyblend A and B. Analysis from FTIR showed compatible of poliblend because it did not have a new function group and did not change of wavelength. Data of tensile strength showed lower value after biodegradation at polyblend C and from DTA and Viscometre showed lower melting point and lower average molecule weight, respectively.

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