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INDONESIA
JURNAL KIMIA SAINS DAN APLIKASI
Published by Universitas Diponegoro
ISSN : 14108917     EISSN : 25979914     DOI : -
urnal Kimia Sains dan Aplikasi (p-ISSN: 1410-8917) and e-ISSN: 2597-9914) is published by Department of Chemistry, Diponegoro University. This journal is published four times per year and publishes research, review and short communication in field of Chemistry.
Arjuna Subject : -
Articles 4 Documents
Search results for , issue "Vol 25, No 5 (2022): Volume 25 Issue 5 Year 2022" : 4 Documents clear
Functionalized Alkaline Lignin for Removal of Lead in Aqueous Solution Deliana Dahnum; Egi Agustian; Eka Triwahyuni; Anis Kristiani; Roni Maryana; Yanni Sudiyani
Jurnal Kimia Sains dan Aplikasi Vol 25, No 5 (2022): Volume 25 Issue 5 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (954.338 KB) | DOI: 10.14710/jksa.25.5.192-196

Abstract

Lignin, the second most abundant natural polymeric globally, is considered the source of the renewable aromatic compound. It serves as an alternative feedstock for the elaboration of chemicals and polymers. However, even until now, it is still primarily used as a low-value fuel for boilers. In the current research, alkaline lignin was modified and used as an adsorbent for removing lead (Pb) in an aqueous solution. The functionalized alkaline lignin (FAL) was prepared by a Mannich reaction with formaldehyde and dimethylamine, followed by esterification of carbon disulfide. The FAL was characterized using CHN elemental analysis, X-Ray Fluorescence (XRF), Scanning Electron Microscopy (SEM), and Fourier Transform Infrared (FT-IR) to observe the changes in composition, morphology, and chemical structure. The analysis revealed that alkaline lignin was successfully modified using amine and carbon disulfide. The adsorption study shows that the lead concentration reduced to 93.7% after 2 hours in contact with FAL. The FAL adsorption capacity could obtain 0.44 mmol/g of lead.
Molecular Docking Study of IPBCC.08.610 Glucose Oxidase Mutant for Increasing Gluconic Acid Production Shobiroh Nuur' Alimah; Tony Ibnu Sumaryada; Waras Nurcholis; Laksmi Ambarsari
Jurnal Kimia Sains dan Aplikasi Vol 25, No 5 (2022): Volume 25 Issue 5 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1286.493 KB) | DOI: 10.14710/jksa.25.5.169-178

Abstract

Glucose oxidase (GOD) is an oxidoreductase enzyme that catalyzes the oxidation of glucose to gluconolactone and hydrogen peroxide. Then, gluconolactone will be hydrolyzed to gluconic acid. The wide application of gluconic acid in various industries has increased production demand. However, glucose concentrations higher than 40% (w/w) inhibited the conversion of glucose to gluconic acid due to a decrease in the oxygen solubility concentration at pH 6, 30℃, and 1 bar pressure. Therefore, decreasing the value of Km is predicted to reduce saturation and enhance gluconic acid production. This study aimed to analyze the interaction between the IPBCC.08.610 GOD mutant with β-D-Glucose in improving gluconic acid production by decreasing the Km value. Mutations were performed in silico using Chimera and then docked using AutoDock Vina. The mutations resulted in distinct ligand poses in the binding pocket, different -OH conformations of the ligands, and changes in the T554M/D578P mutant’s hydrophobicity index (554 mutated from threonine to methionine, and 578 mutated from aspartate to proline), and decreased ΔG and Km values in the H559D mutant (559 mutated from histidine to aspartate), D578P and T554M/D578P. This decrease might strengthen the ligand-receptor interaction, increasing gluconic acid production. The H559D was the best mutant to increase production based on the ΔG, Km value, and stability due to the addition of hydrogen bonds.
Synthesis of Surfactant-Modified Activated Carbon (SMAC) Above Critical Micelle Concentration as Cr(VI) Ion Adsorbent Arnelli Arnelli; Sri Guswini; Ahmad Suseno
Jurnal Kimia Sains dan Aplikasi Vol 25, No 5 (2022): Volume 25 Issue 5 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (364.731 KB) | DOI: 10.14710/jksa.25.5.179-184

Abstract

The synthesis of surfactant-modified activated carbon (SMAC) has been widely studied. However, no research has been conducted to study SMAC concentrations higher than the critical micellar concentration. Therefore, in this study, SMAC was synthesized using anionic and cationic surfactants above CMC (Critical Micelle Concentration) and compared with SMAC below CMC and coconut husk-based activated carbon. This study aimed to determine the surface profile of SMAC and the characteristics and mechanism of metal ion adsorption by SMAC. The selected metal ions were Cr(VI) cations and NH4+ cations as a reference. SMAC was prepared by modifying coconut shell-based activated carbon with anionic surfactant SLS (Sodium Lauryl Sulfate) and cationic surfactant HDTMA-Br (Hexadecyl Trimethyl Ammonium Bromide). Modification of SMAC was performed by three different methods: (a) activated carbon was added gradually with SLS followed by HDTMA-Br, (b) activated carbon was added with HDTMA-Br followed by SLS, (c) activated carbon was mixed with SLS and HDTMA-Br simultaneously. All synthesized SMAC were characterized using FTIR, GSA (Gas Sorption Analyzer), and zeta potential. The FTIR analysis results showed that the synthesized SMAC comprised S=O and (CH3)3N+ groups derived from surfactants. GSA analysis revealed that SMAC has a surface area of 36.790 m2/g, and it was more stable than activated carbon according to the zeta potential result. In this study, the efficiency of SLS and HDTMA-Br in synthesizing SMAC was 99.98% and 95.85%, respectively. SMAC synthesis using method c resulted in Cr(VI) adsorption efficiency of 93.50% and NH4+ adsorption efficiency of 87.37%. In comparison, SMAC below CMC has adsorption capacities of 93.41% for Cr(VI) and 85.05% for NH4+, respectively, whereas Cr(VI) adsorption efficiency by coconut shell-based activated carbon was 99.98%.
Synthesis and Tyrosinase Inhibitory Activity of (E)-5-Benzyl-7- (3-Bromobenzylidene)-3-(3-Bromophenyl)-2-Phenyl-3,3a, 4,5,6,7-Hexahydro-2H-Pyrazolo[4,3-c]Pyridine Nelly Oscifiani; Noval Herfindo; Rahayu Rahayu; Neni Frimayanti; Adel Zamri
Jurnal Kimia Sains dan Aplikasi Vol 25, No 5 (2022): Volume 25 Issue 5 Year 2022
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (412.312 KB) | DOI: 10.14710/jksa.25.5.185-191

Abstract

The tyrosinase enzyme plays an essential role in the pigmentation of human skin, fruits, and vegetables. It has been tied with several human skin diseases and post-harvest problems. Hence, the tyrosinase enzyme becomes an excellent therapeutic target to overcome these issues. This study aimed to screen tyrosinase inhibitors by synthesizing halogen-substituted pyrazolopyridine derivatives. The pyrazolopyridine compound was obtained through two stages of synthesis. First, the intermediate compound, a derivative of 3,5-bis(arylidene)-4-piperidone, was synthesized through the Cleisen-Schmidt condensation reaction of 4-piperidone and benzaldehyde derivatives. Furthermore, the intermediate compound was reacted with phenylhydrazine through a cyclocondensation reaction to produce the titled compound with an 11% yield. The chemical structure of the target compound was identified through the interpretation of UV, FTIR, NMR, and HRMS spectra. Then an in vitro assay was conducted on the tyrosinase enzyme of the fungus Agaricus bisporus by detecting the presence of dopachrome at a wavelength of 492 nm. As a result, the in vitro assay showed that the titled compound had a weak inhibitory activity, and the IC50 value was > 500 µM. Thus, the synthesized compound is considered inactive.

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