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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 25 Documents

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Search results for , issue "Vol 17, No 3 (2017)" : 25 Documents clear

New Trident Molecule with Phosphoric Acid Functionality for Trivalent Rare Earth Extraction Keisuke Ohto; Hiromasa Murashima; Hiroshi Murakami; Shintaro Morisada; Hidetaka Kawakita; Marco Wenzel; Jan J. Weigand; Karsten Gloe
Indonesian Journal of Chemistry Vol 17, No 3 (2017)
Publisher : Universitas Gadjah Mada

Tripodal extraction reagent with three phosphoric acid groups, together with the corresponding monopodal molecule has been prepared to investigate some metals extraction behavior, in particular, trivalent rare earth elements (REEs). The tripodal reagent exhibited extremely high selectivity for metals with high valency such as Zr(IV), In(III), Lu(III), and Fe(III). Tripodal reagent also exhibited exceptionally high extraction ability compared with the corresponding monopodal one in the extraction of trivalent rare earths. The result for the stoichiometry of tripodal reagent to heavy rare earths showed the inflection point between Er (2:1 for a ligand with ion) and Tm (1:1). The extraction reactions were determined for all rare earths with both reagents. The extraction equilibrium constants (Kex), the separation factors (β), half pH values (pH1/2), difference half pH values (ΔpH1/2) for extraction of REEs with both reagents are estimated.

Determination of Effective Functional Monomer and Solvent for R(+)-Cathinone Imprinted Polymer Using Density Functional Theory and Molecular Dynamics Simulation Approaches Andrian Saputra; Karna Wijaya; Ria Armunanto; Lisa Tania; Iqmal Tahir
Indonesian Journal of Chemistry Vol 17, No 3 (2017)
Publisher : Universitas Gadjah Mada

Determination of effective functional monomer and solvent for R(+)-cathinone imprinted polymer through modeling has been done using density functional theory (DFT) and molecular dynamics (MD) simulation approaches. The selection criteria of the best monomer and solvent are based on the classical potential energy (ΔEMM) from molecular dynamics simulation and confirmed further by quantum potential energy (ΔEDFT) from DFT calculation. The DFT calculation was performed in B3LYP exchange-correlation functional within the 6-31G(d) basis set of function including Polarizable Continuum Model (PCM) solvation effect. From this research, it is obtained that N,N’-methylene bis acrylamide and chloroform are respectively the best candidates for effective functional monomer and solvent, for the synthesis of R(+)-cathinone imprinted polymer.

Conocarpus erectus Leaf Extract for Green Synthesis of Silver Nanoparticles Amjed Mirza Alsultani
Indonesian Journal of Chemistry Vol 17, No 3 (2017)
Publisher : Universitas Gadjah Mada

Silver nanoparticles (SNPs) were synthesized by a green method using Conocarpus erectus leaves extract. Leaves were cleaned and used freshly then the extract was obtained by heating leaves in water for 15 min. Silver nitrate used as SNPs precursor and 5 mL of extract were added to silver ion solution at 80 °C and the growth of nanoparticle was monitored by electronic spectra at plasmon resonance absorption of SNPs, where the growth obeys sigmoidal kinetics. SNPs were characterized by SEM, XRD, FTIR, UV-vis absorption and fluorescence, and particle size was estimated. SEM reveals that the SNPs had spherical shape and particle size less than 100 nm. XRD analysis showed that only Ag phase was present and the estimated particle size was 20 nm. FTIR spectra analysis showed similarity of extract and SNPs, indicating the adsorption of active components of the extract on the high surface area of SNPs. Electronic absorption and fluorescence spectroscopy showed that plasmon absorption and fluorescence in the visible region were a characteristic feature of SNPs. Antibacterial activity examined against Escherichia coli and Staphylococcus aureus indicated that the inhibition zones were equal to 24 and 19 mm, respectively.

Investigation of the Structural and Dynamical Properties of Cu+ in Liquid Ammonia: A Quantum Mechanical Charge Field (QMCF) Molecular Dynamics Study Wahyu Dita Saputri; Karna Wijaya; Ria Armunanto
Indonesian Journal of Chemistry Vol 17, No 3 (2017)
Publisher : Universitas Gadjah Mada

A quantum mechanical charge field (QMCF) molecular dynamics (MD) simulation has been carried out to describe the structural and dynamical properties of Cu+ ion in liquid ammonia. The first and second shells were treated by ab initio quantum mechanics at the Hartree−Fock (HF) level with the DZP-Dunning basis set for ammonia and LANL2DZ ECP basis set for Cu. The system was equilibrated for 4 ps, then the trajectory data was collected every fifth step for 20 ps at 235.15 K. The structural analysis showed that in the first solvation shell, Cu+ is solvated by 4 ammonia molecules forming a stable structure of tetrahedral with Cu-N bond length of 2.15 Å, whereas in the second solvation shell there are 29 ammonia molecules that have an average distance of 4.79 Å to Cu+ ion. Mean residence time of 3.06 ps was observed for the ammonia ligand in the second solvation shell indicating for a highly unstable structure of the solvation shell. The obtained structure of the first solvation shell from this simulation is in excellent agreement with experimental data.

Investigation on the Effect of Addition of Fe3+ Ion into the Colloidal AgNPs in PVA Solution and Understanding Its Reaction Mechanism Roto Roto; Marcelina Marcelina; Nurul Hidayat Aprilita; Mudasir Mudasir; Taufik Abdillah Natsir; Bella Mellisani
Indonesian Journal of Chemistry Vol 17, No 3 (2017)
Publisher : Universitas Gadjah Mada

Analysis of Fe3+ ion present in aqueous solutions is always of interests. Recently, this ion has been analyzed by colorimetric methods using colloid of silver nanoparticles (AgNPs) in capping agents of polymers. The reaction mechanism between AgNPs and Fe3+ is still subject to the further investigation. In this work, 1,10-phenanthroline was used to probe the reaction mechanism between AgNPs and Fe3+ ion in the solution. The colloids of AgNPs were prepared in the polyvinyl alcohol (PVA) solution and reacted with Fe3+. The colloid surface plasmon absorbance decreases linearly along with the increase in Fe3+ concentration. The addition of 1,10-phenanthroline to mixture changes the solution to red, indicating that the reaction produces Fe2+. This suggests that the reduction of the AgNPs absorbance is the result of oxidation of the Ag nanoparticles along with the reduction of Fe3+.

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