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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 796 Documents
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Silver Recovery from E-Waste Printed Circuit Board Using Binary and Ternary Deep Eutectic Solvents Arrizal Abdul Aziz; Abraham Mora; Soja Siti Fatimah; Omay Sumarna; Hufaidatul Azfa Nurusyifa; Sheren Hana Elia; Ira Kamilia Siti Huwaidah
Jurnal Kimia Sains dan Aplikasi Vol 27, No 2 (2024): Volume 27 Issue 2 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.27.2.64-71

Abstract

Printed Circuit Boards (PCBs) are essential components of electronic devices containing valuable silver metal. Using sustainable methods, silver recovery from electronic trash, like PCBs, demonstrates excellent promise. This research’s objective is to determine the optimum leaching time and solid-to-liquid (S/L) ratio for extracting silver from PCB using deep eutectic solvent (DES) composed of choline chloride and glycerol (glyceline DES). The binary DES’s leaching performance was then compared to choline chloride, glycerol, and citric acid ternary systems. Fourier Transform Infrared Spectroscopy (FTIR) was carried out to analyze the bond interactions. X-ray fluorescence spectrometry (XRF) was employed to determine the PCB’s metal concentration prior to and after the leaching process. Ternary DES was viscous, colorless, stable for 60 days, and less acidic than binary DES, with a 1.21 g/mL density. FTIR peak broadening and shifting indicated the formation of a new hydrogen bond and proved a successful synthesis of ternary DES. XRF result showed that PCB’s initial silver metal content was 2.32%. The optimal silver leaching from PCB using glyceline DES was achieved after 16 hours, with a 1/20 solid-to-liquid ratio. Ternary DES demonstrated a silver leaching efficiency of 93.65%, surpassing 86.77% of glyceline. Ternary DES synthesized in this study has the potential to serve as an efficient and environmentally friendly solvent for extracting silver from PCB, providing a sustainable approach to managing electronic waste.
Production of Biodiesel from Candlenut Seed Oil (Aleurites Moluccana Wild) Using a NaOH/CaO/Ca Catalyst with Microwave Heating Elfrida Siregar; Lisnawaty Simatupang; Jhony Hartanta Sembiring; Elfrida Ginting
Jurnal Kimia Sains dan Aplikasi Vol 27, No 1 (2024): Volume 27 Issue 1 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.27.1.21-27

Abstract

Oil fuels derived from fossils are non-renewable, so over time, they will run out and have a negative impact on air pollution. To overcome this, there is a need for environmentally friendly alternative fuels from renewable sources such as biodiesel. This research used microwave heating with a CaO catalyst. NaOH-impregnated snail shells and active carbon support. This research aims to determine the effect of power on the conversion of candlenut seed oil into biodiesel using the NaOH/CaO/CA catalyst both in terms of compliance with the SNI 7182-2015 standard and analysis using GC-MS (Gas Chromatography-Mass Spectrometry). The synthesis of the NaOH/CaO/CA catalyst was carried out through wet impregnation and calcination at a temperature of 500°C and analyzed using gas sorption analysis (GSA). Then proceed to the transesterification process, where the power for microwave heating was varied to 300, 450, and 600 watts with a mole ratio of esterified oil and methanol, namely 1:10 for 3 minutes. The analysis results of the NaOH/CaO/CA catalyst using the GSA instrument have a surface area of 9.306 m2/g, pore volume of 0.033 cc/g, and pore diameter of 14.043 nm. Meanwhile, the results of the biodiesel analysis showed that the optimum biodiesel yield was 85.625% at 600 watts of power and had a kinematic density and viscosity that met the SNI 7182-2015 biodiesel standards. Analysis of biodiesel characteristics using GC-MS showed that the three most optimum biodiesel components were hexadecanoic acid, methyl ester (22.664%), 9,12-Octadedecadienoic acid (Z,Z)-, methyl ester (30.176%) and 9-Octadecenoic acid (Z)-, methyl ester (38.656%).
Molecular Properties of Carboxymethyl Chitosan and Its Complexes with Curcumin and Nicotinamide in Drug Delivery Applications: Molecular Docking and Molecular Dynamic Study Luthfiyah Hana Afiyah; Dwi Hudiyanti; Muhammad Cholid Djunaidi; Vivitri Dewi Prasasty; Suci Zulaikha Hildayani; Parsaoran Siahaan
Jurnal Kimia Sains dan Aplikasi Vol 27, No 4 (2024): Volume 27 Issue 4 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.27.4.160-166

Abstract

Carboxymethyl chitosan (CMCs) is a chitosan-derived compound usually used as a carrier matrix in drug delivery systems. There are three types of CMCs based on the location of carboxyl group substitution: N-CMCs, O-CMCs, and N,O-CMCs. The ability of CMCs as a carrier is related to the ability of CMCs to interact with drug molecules. In this work, curcumin and nicotinamide were used as drug models. The ability of CMCs to interact with drug models can be observed by the amount of interaction energy generated when CMCs interact with curcumin and nicotinamide. The purpose of this study is to determine the interaction energy generated when CMCs interact with curcumin and nicotinamide using molecular docking and molecular dynamic methods. The results showed the interaction energy between O-CMCs, N-CMCs, and N,O-CMCs (2 and 3 monomers) with curcumin and nicotinamide, respectively, ranged from -17.08 to -13.37 and -12.05 to -11.00 Kj/mol. Conformational changes in molecular dynamic simulations affect bond-free energy, RMSD, and potential energy complex values.
Total Phenolic, Flavonoid, and LC-MS Analysis of the Ethanolic Extract of Matoa (Pometia pinnata) Leaves from Kudus, Central Java, Indonesia Adhina Choiri Putri; Tri Novia Yuliana; Meiny Suzery; Agustina Lulustyaningati Nurul Aminin
Jurnal Kimia Sains dan Aplikasi Vol 26, No 12 (2023): Volume 26 Issue 12 Year 2023
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.26.12.477-482

Abstract

Matoa (Pometia pinnata) is a plant used as a floral identity in Indonesia, especially in Papua. Local people use boiled water from matoa leaves, which is believed to treat hypertension. Matoa leaves are traditionally used as a therapeutic agent for burns and wounds in Indonesia. Phytochemical screening of matoa leaf extract contains secondary metabolite compounds, including flavonoids, steroids, tannins, and saponins. So far, many of these activities have been reported from the polyphenol group. This research aimed to identify the phytochemical composition of matoa leaves from Kudus in the ethanolic extract using LC-MS. The total phenolic content of ethanol extract using the Folin Ciocalteu method was 35.689 ± 0.726 mg GAE/g extract. The total flavonoid content of ethanol extract using the AlCl3 colorimetric method was 1.384 ± 0.012 mg QE/g extract. Twelve compounds could be identified in the ethanol extract of matoa leaves. The phenolic compounds were vanillin, p-hydroxybenzaldehyde, p-Coumaroyl glycolic acid, syringic acid, gallic acid, phenol, and vanillic acid. The flavonoid compounds were identified as epigallocatechin and apigenin -7-O-diglucuronide. The organic compound was identified as jasmonic acid. The aromatic compound was identified as benzene. Besides, tannin compounds were also identified. The major compounds in matoa leaves from Kudus, Central Java, are vanillin, phenol, and benzene.
Optimization of Cadmium Removal Using Tetraethylene Glycol-Modified Silica-Based Adsorbent via Response Surface Methodology Roza Linda; Abdullah Abdullah; Afrianto Daud; Lisa Aprilia Indriyani; Henny Purwaningsih; Mohamad Rafi; Lee Wah Lim
Jurnal Kimia Sains dan Aplikasi Vol 27, No 3 (2024): Volume 27 Issue 3 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.27.3.128-136

Abstract

In solid-phase extraction for preconcentration, silica (Si) is the most commonly used as an adsorbent. However, the selectivity and effectiveness of silica gel adsorption on metal ions are low, so it needs to be modified to improve the adsorption capability. The modification was done using reflux and oven heating in the modification silica with 3-glycidoxypropyl trimethoxysilane (GPTMS) and tetraethylene glycol (TEG). A central composite design batch process determined the optimum conditions for cadmium adsorption. TEG-modified silica was successfully synthesized and characterized using FTIR spectroscopy, SEM, and elemental analyzers. Peaks of C-H and epoxy on FTIR spectra showed that Si- GPTMS was formed. The increase of %C and %H from the first to the second step indicated that Si-TEG was successfully synthesized. There was no significant difference in silica particle morphology on SEM before and after modification. The reflux method gave a higher yield compared to the heating method. The constant stirring by the magnetic bar and solvent cycle in the reflux method catalyzed the reaction. This study found that at pH 7, 30 mg of adsorbent weight at 35°C and 22 minutes of contact time were optimum Cd2+ adsorption conditions. As the weight of the adsorbent increases, the adsorption capacity decreases. Contact time and temperature have no significant effect on Cd adsorption by Si-TEG.
Modification and Application Study of Activated Natural Zeolite for the Treatment of Liquid Waste from Chemical Laboratory Liqanatul Putri Sholikah; Sumari Sumari; Yuneta Dwi Yunisari
Jurnal Kimia Sains dan Aplikasi Vol 26, No 9 (2023): Volume 26 Issue 9 Year 2023
Publisher : Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.14710/jksa.26.9.332-343

Abstract

Natural zeolite from Malang Regency is a raw material that can be used as an adsorbent for heavy metal waste. However, this natural zeolite needs activation and optimization to be utilized maximally as an adsorbent. This study was conducted for both physical and chemical activation of natural zeolite. Characterization results of XRD indicated that the natural zeolite possesses crystalline phases and is of the mordenite type. Based on the XRF results, the Si/Al ratio increased from 5.768 to 6.119 after activation. Based on the characterization results using the BET method with SAA analysis, the surface area of non-activated natural zeolite was determined to be 20.8045 m²/g, while activated natural zeolite had a surface area of 137.8196 m²/g. Results of the adsorption study in treating liquid laboratory waste using simulated Pb and Cr metal wastes demonstrated that activated natural zeolite performed more effectively as an adsorbent than non-activated natural zeolite. The adsorbent’s optimum mass was 0.3 grams, resulting in an adsorption percentage of 97.43% for Pb and 97.56% for Cr, with a contact time of 30 minutes at pH 6. The adsorption kinetics of Pb and Cr metals were described using a pseudo-second-order rate equation. The adsorption of Pb and Cr was depicted using the Langmuir equation, indicating the monolayer formation on the homogenous adsorbent surface during the adsorption process. The activated natural zeolite has the potential to be employed as an independent adsorbent in the treatment of heavy metal waste.
Formulation and Synthesis of Vanillin from Clove Oil as a Chemosensor for Urea Detection in Urine Adyatma Bhagaskara; Mefi Nur Fadzila; Gavriel Hagai Paulus Sumlang; Sabrina Gita Pramesti; Nur Azis; Jumina Jumina
Jurnal Kimia Sains dan Aplikasi Vol 27, No 2 (2024): Volume 27 Issue 2 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.27.2.72-82

Abstract

Urea levels in urine play an important parameter in diagnosing bodily conditions through liver and kidney examinations. The typical reagent for detecting urea content in urine is para-dimethylaminobenzaldehyde (pDMAB). However, it has a drawback related to the instability of color in the resulting Schiff base compound (pDMAB-urea). In this study, the synthesized vanillin compound derived from clove oil serves as the foundational material for a urea chemosensor based on the colorimetric concept. The synthesized vanillin was characterized using FTIR, GC-MS, and 1H-NMR. The formulation of the vanillin compound as a sensor was conducted by assessing the suitable solvent, determining the optimal mass of vanillin, and evaluating the acid-base conditions of the sensor formulation system both qualitatively and quantitatively. Subsequently, the most effective formulation was selected for detecting urea in urine samples. The synthesis of vanillin yielded a purity level of 95%. The optimal formulation was obtained at an optimum mass of vanilla of 0.75 g in 50 mL of 96% ethanol and 10 mL of 10% NaOH. The color change in the sample was from colorless to greenish yellow (436 nm). The vanillin obtained was applied to urine samples with the best results at a sample dilution level of 10,000×.
Synthesis of Molecularly Imprinted Polymers with Magnetite Cores for Ibuprofen Adsorption Halimah Fahri; Muhammad Ali Zulfikar; Muhammad Yudhistira Azis
Jurnal Kimia Sains dan Aplikasi Vol 27, No 1 (2024): Volume 27 Issue 1 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.27.1.28-34

Abstract

Ibuprofen (IBP) is a pollutant that is widely found in aquatic environments due to pharmaceutical waste and the metabolic results of humans who consume the drug. These compounds can cause damage to aquatic ecosystems, genotoxicity, and aquatic toxicity and are harmful to human health. This study aims to selectively adsorb IBP using magnetic molecularly imprinted polymers (MMIPs) synthesized from ibuprofen (IBP) as a template molecule, methacrylic acid (MAA) as a functional monomer, and divinylbenzene (DVB) as a crosslinker with a mole ratio of 1:4:20 in acetonitrile porogen solvent using a bulk polymerization method. Fe3O4 nanoparticles and MMIPs were characterized using X-ray diffraction (XRD), Fourier Transform Infra-Red (FTIR), and Scanning Electron Microscope (SEM). IBP adsorption reached optimum conditions at pH 3 with a contact time of 90 minutes and a mass of 25 mg of adsorbent. The adsorption performance of MMIPs for IBP was evaluated by adsorption isotherms and adsorption kinetics. Adsorption of IBP by MMIPs followed the Langmuir adsorption isotherm model with an adsorption capacity of 227.24 mg/g. Kinetic studies showed that the adsorption process followed a pseudo-second-order adsorption kinetic model. MMIPs can adsorb IBP selectively even in the presence of interfering compounds, are easily separated from the solution, and can be used repeatedly with good adsorption ability. Hence, it is efficient and promising for removing IBP from aqueous media.
Performance Evaluation of Bentonite/Nano-SiO2 Composite as Bleaching Earth in Crude Palm Oil Processing Agung Kurnia Yahya; Enny Nurmalasari; Apsari Puspita Aini; Hana Nikma Ulya
Jurnal Kimia Sains dan Aplikasi Vol 27, No 4 (2024): Volume 27 Issue 4 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.27.4.167-173

Abstract

In crude palm oil (CPO) processing industries, bleaching is important to remove unwanted impurities. Most industries use various bleaching earth with 0.8-2% w/v concentration during the bleaching process. As bleaching earth is single-used for the bleaching process, materials with higher adsorption ability are preferable to reduce the use of bleaching earth. This study aimed to evaluate the performance of bentonite/nano SiO2 composite (BE-SiO2) as bleaching earth in the bleaching process of CPO. The prepared BE-SiO2 was used in the bleaching process with various BE-SiO2 concentrations (0.1-1.3% w/v), process duration (0-2.5 hours), and process temperature (70-150°C). From the results, the rise in BE-SiO2 concentration during the CPO bleaching process initially led to a decrease in the β-carotene concentration, acid content, free fatty acids (FFA), and DOBI number up to 1% w/v of BE-SiO2. Subsequently, these parameters exhibited an increase with the addition of BE-SiO2. The bleaching process effectively reduced the β-carotene concentration, acid content, FFA, and DOBI number within the first 1.5 hours of operation. While a higher amount of β-carotene was adsorbed during the adsorption process at higher temperatures, the bleached palm oil (BPO) quality was compromised due to the heat. The results showed that the most effective condition of the bleaching process was performed with 1% w/v BE-SiO2 concentration for 1.5 hours at 90°C. From those conditions, the BPO had a β-carotene concentration of 312.311 ppm, water content of 0.112%, acid number of 0.0076, FFA of 4.864%, DOBI number of 1.311, and red/yellow of 1.5/15.
Endophytic Bacteria Producing Alkaloid as Antibacterial and Antioxidant Agent from Hibiscus tiliaceus Leaves Purbowatiningrum Ria Sarjono; Aulia Anggraeni; Ismiyarto Ismiyarto; Ngadiwiyana Ngadiwiyana
Jurnal Kimia Sains dan Aplikasi Vol 27, No 3 (2024): Volume 27 Issue 3 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.27.3.137-144

Abstract

Hibiscus tiliaceus is known to have antibacterial activity. One of the antibacterial compounds contained in the hibiscus plant is alkaloid. Alkaloids can also be obtained from endophytic bacteria that are in symbiosis with hibiscus leaves. It is known that endophytes can produce the same or similar secondary metabolites as their host plants. Medicinal plants have been proven to be a source of microorganisms that can make certain metabolites. Our previous research succeeded in isolating the endophytic bacteria Staphylococcus warneri strain 25 from waru leaves (Hibiscus tiliaceus), which had antioxidant and antibacterial activity and contained saponins and alkaloids. In this study, alkaloids were extracted from the endophytic bacteria found in waru leaves. Subsequently, their bioactivity was assessed for antibacterial properties against Escherichia coli, Salmonella typhi, and Staphylococcus aureus using the well diffusion method. Additionally, their antioxidant activity was evaluated through the DPPH method, with gallic acid serving as the standard. A cyclic amine alkaloid compound was isolated, exhibiting a Minimum Inhibitory Concentration (MIC) of 23 ppm against E. coli, S. typhi, and S. aureus bacteria, accompanied by inhibitory zones measuring 7 mm, 8 mm, and 6 mm, respectively. Additionally, the compound had very strong antioxidant activity, with an IC50 value of 50.11 ppm.

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