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JURNAL KIMIA SAINS DAN APLIKASI
Published by Universitas Diponegoro
ISSN : 14108917     EISSN : 25979914     DOI : -
Core Subject : Science, Engineering,
Chemical Engineering, Chemistry & Bioengineering Chemistry Engineering
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.
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Articles 804 Documents
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Green Synthesis of Gold Nanoparticles Using Basella alba Leaf Extract and Their Antioxidant Activity Nur Rizka Aprilia; Titik Taufikurohmah
Jurnal Kimia Sains dan Aplikasi Vol 27, No 8 (2024): Volume 27 Issue 8 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.8.381-387

Abstract

In this research, gold nanoparticles were synthesized using the green synthesis method with the bioreduction extract of Basella alba leaf infusion. This research aims to characterize gold nanoparticles synthesized using UV-Vis spectroscopy and TEM and assess their antioxidant activity, which is quantified by the IC50 value. The UV-Vis spectrophotometric characterization of the gold nanoparticles revealed an absorption peak at a maximum wavelength of 543 nm. TEM characterization indicated a particle diameter of 9.463 ± 2.273 nm. The antioxidant activity was evaluated using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) reduction method with concentration variations of 2.5, 5, 10, and 20 ppm, resulting in reduction percentages of 40.6%, 44.3%, 57.4%, and 77.9%, respectively, and an IC50 value of 7.05 μg/mL, indicating very strong antioxidant activity. Based on these findings, it can be concluded that Basella alba leaf infusion extract is effective as a biological reducing agent in synthesizing gold nanoparticles, and the resulting nanoparticles show significant potential as antioxidants for reducing free radicals.
Na₂SO₃ Salt Effect on The Ionic Conductivity of Solid Polymer Electrolyte (SPE) Based on Polyvinyl Alcohol Sylvia Ayu Pradanawati; Albert Turnip; Nur Laila Hamidah; Yose Fachmi Buys
Jurnal Kimia Sains dan Aplikasi Vol 27, No 5 (2024): Volume 27 Issue 5 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.5.197-204

Abstract

This research is about solid polymer electrolyte (SPE) based on polyvinyl alcohol (PVA) synthesized using a solution casting technique by adding variations of sodium sulfite salt and glycerol as fillers to reduce the samples' bulk resistance for electrochemical energy storage application. The method used is a quantitative analysis based on the test results. X-ray Diffraction (XRD) was used to determine the crystallinity and structure of the solid polymer electrolyte material. Interactions between Na+ ions from salts in SPE were analyzed using Fourier transform infrared (FTIR). The mechanical properties of the SPE samples were analyzed using tensile testing (ultimate tensile strength). Solid polymer electrolyte (SPE) ion conductivity was analyzed using electrochemical impedance spectroscopy (EIS) with temperature variations of 25, 40, 50, 60, and 70°C. The maximum SPE ionic conductivity value is 1.05 × 10-5 S cm-1 in a PVA-Glycerol-Na2SO3 15% sample at 70°C.
Comparison of the Lipoamide Synthesis by Direct Amidation and via Amidation of Fatty Acid Methyl Esters Chiko Harahap; Tuti Wukirsari; Sri Handayani; Sumi Hudiyono PWS
Jurnal Kimia Sains dan Aplikasi Vol 27, No 7 (2024): Volume 27 Issue 7 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.7.328-335

Abstract

In this research, the preparation of lipoamide through direct amidation of fatty acid and via amidation of fatty acid methyl ester (FAME) was compared. The reactivity of aromatic amines and cyclohexylamine for the synthesis of lipoamide was investigated in this research. The performance of saturated and unsaturated fatty acids was also compared. The synthesis of lipoamides via direct amidation was conducted under reflux using a Dean-Stark trap and silica gel as the catalyst. On the other hand, the amidation of FAME was carried out without catalysts and solvent. Both reactions were run simultaneously for 18 hours at the same temperature. The reaction was monitored using TLC, and then the product was purified using column chromatography and characterized using FTIR and 1H NMR. The TLC data, FTIR, and 1H NMR spectra confirmed that both reaction pathways produced the same lipoamide as the product. Both reaction pathways were compatible with aromatic and nonaromatic amines and saturated and unsaturated fatty acids. The reaction yield of lipoamide from direct amidation was around 70-80% and two-fold higher than lipoamide synthesis via amidation of FAME. Therefore, direct amidation of fatty acid was preferred for the synthesis of lipoamides compared to via amidation of FAME.
Synthesis and Characterization of Silica-Biochar Composite as Rhodamine B Dye Adsorbent Lisa Sari; Anis Shofiyani; Ajuk Sapar
Jurnal Kimia Sains dan Aplikasi Vol 27, No 6 (2024): Volume 27 Issue 6 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.6.284-292

Abstract

Composites are synthesized by combining different materials, resulting in properties suitable for use as adsorbents due to the combination of pores and functional groups within the constituent materials. This study developed a silica-biochar composite to serve as an adsorbent for rhodamine B dye, utilizing silica derived from red mud and biochar obtained from oil palm empty fruit bunches (OPEFB). This research focused on analyzing the characteristics and effectiveness of the composite as an adsorbent by varying its composition. Silica from red mud exhibited a purity of 80.05% and possessed silanol (Si-OH) and siloxane (Si-O-Si) functional groups on its surface, whereas biochar from OPEFB had a carbon content of 95.91% and included functional groups such as -OH, C=O, C=C, C-H, and C-O. The combination of silica and biochar yielded a composite surface consisting of -OH, C=O, C=C, C-O, C-H, and Si-O-Si functional groups. The silica-biochar composite demonstrated a greater surface area than its individual components, with silica at 69.824 m²/g and biochar at 95.452 m²/g. The composite with a 1:2 (% w/w) ratio exhibited the largest surface area at 102.371 m²/g, achieving a maximum adsorption capacity of 1.550 mg/g and an efficiency of 88.463%. The adsorption process encompasses physical interactions via pore diffusion and chemical interactions through functional groups.
In Silico Analysis for Exploring the Potential Inhibitors Against Breast Cancer (MCF7) Using Curcumin Analogue Compounds Neni Frimayanti; Adel Zamri; Yum Eryanti
Jurnal Kimia Sains dan Aplikasi Vol 27, No 6 (2024): Volume 27 Issue 6 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.6.250-257

Abstract

Breast cancer is one of the most problematic diseases in the world. Currently, there are no potential vaccines for the treatment of this disease. Therefore, finding effective compounds, such as curcumin analogs, is crucial to inhibit breast cancer. Forty-five synthesized curcumin analogs were tested on the MCF7 cell line using the MTT assay. It was shown that nine curcumin compounds, Cpd 5, Cpd 9, Cpd 17, Cpd 18, Cpd 21, Cpd 25, Cpd 28, Cpd 32, and Cpd 45, had better inhibitory activities against breast cancer. Furthermore, in silico analysis was developed using 2D and 3D QSAR models with high predictive ability, with an r2 value of 0.834. In addition, based on molecular docking, molecular dynamics, and pharmacophore results, it was shown that these nine compounds had the lowest binding free energy and were also stable during the simulation. The presence of methoxy groups, hydrogen bond donors, and aromatic ring features are the main factors that enhance the biological activity of curcumin analogs. Therefore, these compounds could serve as references for the next stage of drug design.
The Effect of Mole Ratio Natural-CaCO₃/KF in the Synthesis of KCaF₃ Perovskite Base Catalyst I. F. Nurcahyo; Eddy Heraldy; Suciana Nur Cahyaningsih; Fitria Rahmawati; Khoirina Dwi Nugrahaningtyas; Yuniawan Hidayat; Firanda Larasati
Jurnal Kimia Sains dan Aplikasi Vol 27, No 8 (2024): Volume 27 Issue 8 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.8.388-394

Abstract

The KCaF3 perovskite catalyst was successfully synthesized by reacting limestone (natural-CaCO3) with potassium fluoride (KF). The synthesis of the KCaF3 catalyst was conducted with several variations in the mole ratio of CaCO3 to KF (1:1, 1:2, and 1:3). The research results showed that the addition of KF can affect the characteristics of the catalyst. The optimal catalyst is the KCaF3 catalyst with a mole ratio variation of 1:3. X-ray diffractometer analysis revealed that the highest KCaF3 phase composition reached 74.05%, while thermogravimetric analysis indicated a CaCO3 concentration of 34.50%. Surface Area Analyzer analysis shows that KCaF3 has the largest surface area, which is 187.1 m2/g. This catalyst efficiently facilitated the transesterification of palm oil, yielding 93.4% biodiesel.
Extraction and Characterization of Silicon Dioxide from Coal Fly Ash as Counter Electrode Material in Dye-Sensitized Solar Cells (DSSCs) Mitha Pratiwi; Leila Kalsum; Rusdianasari Rusdianasari
Jurnal Kimia Sains dan Aplikasi Vol 27, No 9 (2024): Volume 27 Issue 9 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.9.419-425

Abstract

The counter electrode in DSSCs must be made of a material with various advantageous chemical and physical characteristics to guarantee the cell’s efficient functioning and cost efficiency. Coal fly ash is recognized for its substantial silicon dioxide (SiO2) content and other minerals and metals. This paper provides a detailed analysis and description of extracting and characterizing SiO2 from coal fly ash. This extraction aims to utilize SiO2 as a material for the counter electrode in DSSCs. The extraction procedure of SiO2 from coal fly ash involves a multi-step process that entailed the utilization of acid leaching using hydrochloric acid 1 M at 90°C for 4 h, which was subsequently followed by precipitation using NaOH 3 M at 90°C for 4 h to separate SiO2. The SiO2 gel was cleaned of contaminants with hot distilled water and dried at 110°C for 12 h. The SiO2 that was obtained was analyzed utilizing a range of analytical techniques to evaluate its structural, morphological, chemical, and optical properties. The X-ray diffractometer (XRD) examination revealed that the crystal structure of coal fly ash consisted of quartz, corundum, hematite, lime, and periclase. The SiO2 that was obtained exhibited a crystal structure that was both cubic and triclinic. The morphology is visualized using a scanning electron microscope (SEM). The study using atomic absorption spectroscopy revealed that the coal fly ash contained 52.91% SiO2, whereas the extracted SiO2 had a purity of 91.20%. The UV-Vis spectrophotometry investigation revealed that the SiO2 exhibited absorbance spectra with a wide band gap of 4.17 eV, whereas the coal fly ash had absorbance spectra of 3.37 eV.
Extraction of Natural Colorant from Clitoria ternatea Flowers Using Conventional Solvent Extraction (CSE) and Ultrasound-Assisted Extraction (UAE) Techniques: Kinetic Modeling and Compound Stability Pra Cipta Buana Wahyu Mustika; Hadiyatni Rita Priyantini; Eryan Dwi Krisna; Firman Aldani; Fikrah Dian Indrawati Sawali; Moh Azhar Afandy; Mega Mustikaningrum
Jurnal Kimia Sains dan Aplikasi Vol 27, No 11 (2024): Volume 27 Issue 11 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.11.549-559

Abstract

The Clitoria ternatea flowers, a prevalent local commodity in Indonesia, are extensively found, particularly in the East Java region. One approach to enhance the utility and economic significance of these flowers involves isolating their active component, specifically anthocyanin. Anthocyanins have several health benefits, especially in preventing cardiovascular disease, improving vision, and being anti-diabetic, anti-inflammatory, and anti-cancer. The isolation methods used in this research were conventional solvent extraction (CSE) and ultrasonic-assisted extraction (UEA) methods. The use of UAE has been experimentally proven to accelerate the extraction rate of bioactive compounds. This dal is caused by a driving force in the form of energy produced from bubble cavitation resulting from ultrasonic energy. The specific aim of this study was to compare the effectiveness of the two methods in anthocyanin isolation. The extraction stages were carried out at 30, 40, 50, 60, and 70°C operating temperatures, with an S/L ratio of 1:10, 1:15, 1:20:1:25, and 1:30 with samples conditioned in dry and wet conditions. The optimal conditions for ultrasound-assisted extraction (UEA) involve dry samples with a S/L ratio of 1:30 at a temperature of 70°C with the resulting final concentration of 16.5234 g/L. This configuration ensures an efficient extraction process, completed in less than 30 minutes, thereby preventing the degradation of anthocyanins. Analysis indicates that the extraction process adheres to a second-order kinetic model with a constant (k) of 0.1039. Stability testing revealed that the first–order kinetic model accurately represents the impact of temperature on anthocyanin degradation.
Synthesis and Characterization of Reduced Graphene Oxide from Nipah Shell Charcoal (Nypa fruticans Wurmb) using Microwave Irradiation Ilma Fadlilah; Ayu Pramita; Rosita Dwityaningsih
Jurnal Kimia Sains dan Aplikasi Vol 27, No 11 (2024): Volume 27 Issue 11 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.11.510-514

Abstract

Graphene, an allotrope of carbon, consists of a single layer of carbon atoms arranged in a honeycomb lattice and holds significant potential for diverse applications. This study focuses on the synthesis of reduced graphene oxide (rGO) from nipah shell charcoal (Nypa fruticans Wurmb) using a modified Hummer’s method combined with microwave irradiation, employing L-ascorbic acid as the reducing agent. The synthesized rGO was characterized using Fourier Transform Infrared (FTIR) spectroscopy, X-ray Diffraction (XRD), and Scanning Electron Microscopy coupled with Energy Dispersive X-ray analysis (SEM-EDX). The FTIR spectra revealed an aromatic C=C ring stretching vibration at 1591.47 cm-1. The XRD analysis showed characteristic rGO peaks at 2θ ~ 27.58° and 48.45°. SEM images indicated that the rGO exhibited sheet-like structures with slight wrinkling. Elemental analysis identified carbon and oxygen as the primary elements in both GO and rGO, alongside trace impurities, including N, Mg, Al, Si, Ca, Zn, and S. An increase in the C/O ratio from 1.90 in GO to 2.38 in rGO confirmed the successful synthesis of reduced graphene oxide.
Development and Characterization of a Chitosan and Polyvinyl Alcohol (CS/PVP)-Based Slow-Release Urea Fertilizer Membrane Retno Ariadi Lusiana; Khabibi Khabibi; Rahmad Nuryanto; Muhammad Ridho Shofwan Al Aziz
Jurnal Kimia Sains dan Aplikasi Vol 27, No 10 (2024): Volume 27 Issue 10 Year 2024
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.27.10.470-476

Abstract

A slow-release test of urea fertilizer was conducted using chitosan-urea (CS-U) and chitosan/polyvinyl pyrrolidone K30-urea (CS/PVP-U) membranes. The urea membrane synthesis involved a blending method, with PVP K30 added as a component. The slow-release capabilities of CS-U, CS/PVP1-U, CS/PVP2-U, CS/PVP3-U, and CS/PVP4-U membranes were compared. FTIR results showed an increased intensity of the primary NH double peak at 1587 cm-1 and 1640 cm-1, while the C=O spectrum shifted from 1640 to 1647 cm-1 and the -OH group from 3354 cm-1 to 3362 cm-1, indicating hydrogen bond formation in CS/PVP-U. XRD analysis confirmed the membrane’s amorphous structure, and FE-SEM and AFM studies revealed morphology and roughness differences, with CS/PVP4-U having the largest cross-sectional diameter. The release study showed that PVP-modified chitosan membranes increased urea release, achieving 60 ppm/2 days for the first 16 days, then decreasing to about 55 ppm through day 30, with partial urea release controlled over time. This suggests that SRF fertilizer can effectively control urea release into the environment.

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