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%).
{"title":"Production of Biodiesel from Candlenut Seed Oil (Aleurites Moluccana Wild) Using a NaOH/CaO/Ca Catalyst with Microwave Heating","authors":"Elfrida Siregar, Lisnawaty Simatupang, Jhony Hartanta Sembiring, Elfrida Ginting","doi":"10.14710/jksa.27.1.21-27","DOIUrl":"https://doi.org/10.14710/jksa.27.1.21-27","url":null,"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%).","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"69 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140455268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-13DOI: 10.14710/jksa.27.1.28-34
Halimah Fahri, M. A. Zulfikar, Muhammad Yudhistira Azis
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.
{"title":"Synthesis of Molecularly Imprinted Polymers with Magnetite Cores for Ibuprofen Adsorption","authors":"Halimah Fahri, M. A. Zulfikar, Muhammad Yudhistira Azis","doi":"10.14710/jksa.27.1.28-34","DOIUrl":"https://doi.org/10.14710/jksa.27.1.28-34","url":null,"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.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"301 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140457652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Arie Adhi Nugraha, Lanni Rahma Aulia, Meiny Suzery, A. L. Aminin
Solid State Fermentation has been employed for the biotransformation of the herbal plant Hyptis pectinata (L.) Poit is widely distributed in tropical regions of Brazil and is also present in Indonesia. The plant has been used to treat anti-inflammatory, anti-cancer, bacterial infection, and wound healing. This study aims to investigate the effects of using a solid-state fermentation method to ferment the leaves of Hyptis pectinata (L.) Poit towards the composition of phytochemicals and hyptolides. This study was carried out in several stages, including fermentation of Aspergillus niger leaves, sample extraction with methanol, determination of total phenolic and total triterpenoid content, phytochemical screening, and analysis of hyptolide using HPLC. The research results showed the growth of Aspergillus niger on the leaves of Hyptis pectinata (L.) Poit got into the logarithmic phase at 36 hours. Triterpenes and phenolics were present in the phytochemical profile, while alkaloids, tannins, and flavonoids were absent. The total phenolic and triterpenoid content increased by 33.68% and 17.78% respectively. HPLC analysis showed a decrease in hyptolide content in the fermented product. These results indicate the potential of fermented Hyptis pectinata (L.) Poit as an additional cancer therapy.
{"title":"Impact of Fermentation on Hyptolide and Phytochemical Composition of Hyptis pectinata (L.) Poit","authors":"Arie Adhi Nugraha, Lanni Rahma Aulia, Meiny Suzery, A. L. Aminin","doi":"10.14710/jksa.27.1.8-13","DOIUrl":"https://doi.org/10.14710/jksa.27.1.8-13","url":null,"abstract":"Solid State Fermentation has been employed for the biotransformation of the herbal plant Hyptis pectinata (L.) Poit is widely distributed in tropical regions of Brazil and is also present in Indonesia. The plant has been used to treat anti-inflammatory, anti-cancer, bacterial infection, and wound healing. This study aims to investigate the effects of using a solid-state fermentation method to ferment the leaves of Hyptis pectinata (L.) Poit towards the composition of phytochemicals and hyptolides. This study was carried out in several stages, including fermentation of Aspergillus niger leaves, sample extraction with methanol, determination of total phenolic and total triterpenoid content, phytochemical screening, and analysis of hyptolide using HPLC. The research results showed the growth of Aspergillus niger on the leaves of Hyptis pectinata (L.) Poit got into the logarithmic phase at 36 hours. Triterpenes and phenolics were present in the phytochemical profile, while alkaloids, tannins, and flavonoids were absent. The total phenolic and triterpenoid content increased by 33.68% and 17.78% respectively. HPLC analysis showed a decrease in hyptolide content in the fermented product. These results indicate the potential of fermented Hyptis pectinata (L.) Poit as an additional cancer therapy.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"24 8","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140460456","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-06DOI: 10.14710/jksa.27.1.35-44
Resa Wulandari, E. Pramono, S. T. C. L. Ndruru, Abu Masykur, Sayekti Wahyuningsih, Aditya Muhammad Fadhilah, Ellya Syaharani, Elva Yoga Saputra, Mayzy Vanesia Insani
Research on porous membrane technology is proliferating, especially in the process of fabrication of membranes. Different methods in membrane fabrication can affect the physical and chemical properties of the produced membrane. This study aims to investigate the influence of temperature, molecular weight, and non-solvent type on the physical-chemical properties of PVDF membranes. The membrane was produced by the immersion precipitation method with varying PVDF molecular weights of 64 kDa, 352 kDa (Solef 1010), 534 kDa, and 573 kDa (Solef 1015); non-solvent variations of alcohol (methanol, ethanol, isopropyl alcohol, and butanol); and drying temperature variations of 40, 50, and 60°C. The produced membranes were analyzed using ATR-FTIR, XRD, TGA, DSC, and SEM, and their wettability properties were evaluated using water contact angles. The optimal drying temperature for membrane production was 60°C. The ATR-FTIR data showed that molecular weight impacted membrane structure, where PVDF MW 534 kDa membrane had the highest percentage of β phase (77.47%). Non-solvent changes also affected membrane structure; PVDF Solef 1010 with non-solvent isopropyl alcohol had the highest percentage of β phase (67.45%). This is supported by the XRD diffractogram that displayed peaks at 2θ values between 20.24° and 20.66°, indicating the presence of a phase β PVDF. The thermal analysis exhibited three stages of degradation for Solef 1010 with ethanol non-solvent and two for the other seven membranes. The degradation temperature increases with the increase in molecular weight and the difference in non-solvents. The highest thermal stability membrane was PVDF Solef 1010 with isopropyl alcohol non-solvent (430°C). SEM images showed the membrane with non-solvent isopropyl alcohol, displaying a dense sponge-like morphology. The wettability of membranes is affected by molecular weight and non-solvent type. The membrane with isopropyl alcohol non-solvent obtained the smallest contact angle (54.77°) and indicated the most wettability membrane.
{"title":"Effects of Temperature, Molecular Weight, and Non-Solvent Variation on the Physical Properties of PVDF Membranes Prepared through Immersion Precipitation","authors":"Resa Wulandari, E. Pramono, S. T. C. L. Ndruru, Abu Masykur, Sayekti Wahyuningsih, Aditya Muhammad Fadhilah, Ellya Syaharani, Elva Yoga Saputra, Mayzy Vanesia Insani","doi":"10.14710/jksa.27.1.35-44","DOIUrl":"https://doi.org/10.14710/jksa.27.1.35-44","url":null,"abstract":"Research on porous membrane technology is proliferating, especially in the process of fabrication of membranes. Different methods in membrane fabrication can affect the physical and chemical properties of the produced membrane. This study aims to investigate the influence of temperature, molecular weight, and non-solvent type on the physical-chemical properties of PVDF membranes. The membrane was produced by the immersion precipitation method with varying PVDF molecular weights of 64 kDa, 352 kDa (Solef 1010), 534 kDa, and 573 kDa (Solef 1015); non-solvent variations of alcohol (methanol, ethanol, isopropyl alcohol, and butanol); and drying temperature variations of 40, 50, and 60°C. The produced membranes were analyzed using ATR-FTIR, XRD, TGA, DSC, and SEM, and their wettability properties were evaluated using water contact angles. The optimal drying temperature for membrane production was 60°C. The ATR-FTIR data showed that molecular weight impacted membrane structure, where PVDF MW 534 kDa membrane had the highest percentage of β phase (77.47%). Non-solvent changes also affected membrane structure; PVDF Solef 1010 with non-solvent isopropyl alcohol had the highest percentage of β phase (67.45%). This is supported by the XRD diffractogram that displayed peaks at 2θ values between 20.24° and 20.66°, indicating the presence of a phase β PVDF. The thermal analysis exhibited three stages of degradation for Solef 1010 with ethanol non-solvent and two for the other seven membranes. The degradation temperature increases with the increase in molecular weight and the difference in non-solvents. The highest thermal stability membrane was PVDF Solef 1010 with isopropyl alcohol non-solvent (430°C). SEM images showed the membrane with non-solvent isopropyl alcohol, displaying a dense sponge-like morphology. The wettability of membranes is affected by molecular weight and non-solvent type. The membrane with isopropyl alcohol non-solvent obtained the smallest contact angle (54.77°) and indicated the most wettability membrane.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"144 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140460862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. Fachriyah, Sofiana Nur Aziiza, I. Ismiyarto, P. R. Sarjono, D. Hudiyanti, S. Sumariyah
Land kale or Ipomoea reptans Poir is widely consumed by Indonesian people. Land kale plants can be used as natural antioxidants because they contain polyphenolic compounds, one of which is phenolic acid. This research was carried out to determine the antioxidant activity and isolate phenolic acid compounds contained in land kale plants (Ipomoea reptans Poir). The sample used was an ethanol extract of land kale. The total phenolics were determined using the Folin-Ciocalteu method. Phenolic acids were isolated using alkaline hydrolysis and acid hydrolysis and without hydrolysis methods. Separation of isolates was carried out using the TLC method. The structure was identified using UV-Vis spectrophotometry and LC-MS/MS. Antioxidant activity was measured using the DPPH method. The total phenolics of land kale ethanol extract were 71.2420 ± 0.0791 mg/g GAE. TLC showed that the HB, HA, and TH fractions contained caffeic acid and ferulic acid compounds. Separation of the (HB) fraction produced three isolates: B2 with a yellow color, B3 with a slightly yellowish color, and B4 which is colorless. Isolate B2 was identified as potentially containing caffeic acid, while isolate B3 was indicated to potentially contain ferulic acid through analysis using a UV-Vis spectrophotometer. Isolate B4 was thought to have a hydroxybenzoic acid framework after being determined using LC-MS/MS. The ethanol extract of land kale has strong antioxidant activity because it produces an IC50 value of 94.83 mg/L.
{"title":"Isolation of Phenolic Acids from Land Kale (Ipomoea reptans Poir) and Antioxidant Activity","authors":"E. Fachriyah, Sofiana Nur Aziiza, I. Ismiyarto, P. R. Sarjono, D. Hudiyanti, S. Sumariyah","doi":"10.14710/jksa.27.1.1-7","DOIUrl":"https://doi.org/10.14710/jksa.27.1.1-7","url":null,"abstract":"Land kale or Ipomoea reptans Poir is widely consumed by Indonesian people. Land kale plants can be used as natural antioxidants because they contain polyphenolic compounds, one of which is phenolic acid. This research was carried out to determine the antioxidant activity and isolate phenolic acid compounds contained in land kale plants (Ipomoea reptans Poir). The sample used was an ethanol extract of land kale. The total phenolics were determined using the Folin-Ciocalteu method. Phenolic acids were isolated using alkaline hydrolysis and acid hydrolysis and without hydrolysis methods. Separation of isolates was carried out using the TLC method. The structure was identified using UV-Vis spectrophotometry and LC-MS/MS. Antioxidant activity was measured using the DPPH method. The total phenolics of land kale ethanol extract were 71.2420 ± 0.0791 mg/g GAE. TLC showed that the HB, HA, and TH fractions contained caffeic acid and ferulic acid compounds. Separation of the (HB) fraction produced three isolates: B2 with a yellow color, B3 with a slightly yellowish color, and B4 which is colorless. Isolate B2 was identified as potentially containing caffeic acid, while isolate B3 was indicated to potentially contain ferulic acid through analysis using a UV-Vis spectrophotometer. Isolate B4 was thought to have a hydroxybenzoic acid framework after being determined using LC-MS/MS. The ethanol extract of land kale has strong antioxidant activity because it produces an IC50 value of 94.83 mg/L.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"2 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140506455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-30DOI: 10.14710/jksa.26.9.363-371
Jesisca Silver, Surya Lubis, Muliadi Ramli
Zinc oxide (ZnO) nanoparticles have been successfully synthesized using water extract of red dragon fruit (Hylocereus polyrhizus) stem with zinc acetate dihydrate as a precursor of ZnO. Chemical compounds contained in the red dragon fruit stem extract, such as phenolics, terpenoids, and steroids, acted as reducing agents, stabilizers, and capping agents. The phase structure, crystallite size, functional groups, shape, and morphology of ZnO nanoparticles were determined by X-ray diffraction (XRD), Fourier Transform infrared (FT-IR) Spectroscopy, and Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX). The XRD pattern confirmed the crystallinity of synthesized zinc oxide was in the zincite (ZnO) phase with an average crystallite size of 79.09 nm. Spectroscopy FTIR analysis showed that the synthesized ZnO nanoparticles had characteristics similar to the ZnO standard/commercial. SEM-EDX analysis revealed that the synthesized ZnO nanoparticles were spherical, evenly distributed, and homogeneous particle size. The photocatalytic activity of synthesized ZnO nanoparticles was evaluated on the photodegradation of naphthol blue black (NBB) dye. The results showed that the synthesized ZnO nanoparticles have high photocatalytic activity that can degrade NBB dye up to 98.82%. This high photocatalytic activity was obtained at operating parameter conditions with the initial pH of NBB at 2, the dosage of ZnO nanoparticles at 250 mg, and the initial dye concentration at 10 ppm.
{"title":"Green Synthesis, Characterization, and Photocatalytic Activity of Zinc Oxide Nanoparticles on Photodegradation of Naphthol Blue Black Dye","authors":"Jesisca Silver, Surya Lubis, Muliadi Ramli","doi":"10.14710/jksa.26.9.363-371","DOIUrl":"https://doi.org/10.14710/jksa.26.9.363-371","url":null,"abstract":"Zinc oxide (ZnO) nanoparticles have been successfully synthesized using water extract of red dragon fruit (Hylocereus polyrhizus) stem with zinc acetate dihydrate as a precursor of ZnO. Chemical compounds contained in the red dragon fruit stem extract, such as phenolics, terpenoids, and steroids, acted as reducing agents, stabilizers, and capping agents. The phase structure, crystallite size, functional groups, shape, and morphology of ZnO nanoparticles were determined by X-ray diffraction (XRD), Fourier Transform infrared (FT-IR) Spectroscopy, and Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX). The XRD pattern confirmed the crystallinity of synthesized zinc oxide was in the zincite (ZnO) phase with an average crystallite size of 79.09 nm. Spectroscopy FTIR analysis showed that the synthesized ZnO nanoparticles had characteristics similar to the ZnO standard/commercial. SEM-EDX analysis revealed that the synthesized ZnO nanoparticles were spherical, evenly distributed, and homogeneous particle size. The photocatalytic activity of synthesized ZnO nanoparticles was evaluated on the photodegradation of naphthol blue black (NBB) dye. The results showed that the synthesized ZnO nanoparticles have high photocatalytic activity that can degrade NBB dye up to 98.82%. This high photocatalytic activity was obtained at operating parameter conditions with the initial pH of NBB at 2, the dosage of ZnO nanoparticles at 250 mg, and the initial dye concentration at 10 ppm.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"4 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139206366","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-26DOI: 10.14710/jksa.26.9.344-352
Tan David Christian, K. Kasiyati, Tri Yuliani, Ariyanti Saputri, Dadang Priyoatmojo, Marrisa Angelina
Candida albicans is one of the most common fungal species causing opportunistic infections, such as candidiasis. Candida albicans has the ability to produce and secrete hydrolytic enzymes, namely secrete aspartate protease (SAP). SAP3 is a virulence factor for mucosal or disseminated infections. Cassia fistula leaves have bioactive compounds that can be used as antimicrobial agents, such as hyperoside, delphin, epicatechin, isoquercitrin, and astragalin. This study aims to determine the potential of bioactive compounds in Cassia fistula L. as an antifungal by in silico method molecular docking and Minimum Inhibitory Concentration (MIC) analysis with FE-SEM test for microscopical visual results. The results showed that the delphin compound had the best binding energy of -7.73 and an inhibition constant of 2.17 M, almost equivalent to ketoconazole as a positive control. MIC test of ethanol and ethyl acetate extracts of Cassia fistula leaves resulted in 100 ppm in the ethanol extract and 50 ppm in the ethyl acetate fraction. This result was supported by FE-SEM results, which showed that the ethanol extract at 100 ppm could damage the structure of Candida albicans colony.
白色念珠菌是导致机会性感染（如念珠菌病）的最常见真菌之一。白色念珠菌能够产生和分泌水解酶，即分泌天冬氨酸蛋白酶（SAP）。SAP3 是粘膜感染或播散感染的毒力因子。决明子叶中含有可用作抗菌剂的生物活性化合物，如金丝桃苷、脱酚素、表儿茶素、异槲皮苷和黄芪苷。本研究旨在通过分子对接和最低抑菌浓度（MIC）分析，以及显微镜下的 FE-SEM 测试，确定肉桂中的生物活性化合物作为抗真菌剂的潜力。结果表明，delphin 化合物的最佳结合能为-7.73，抑制常数为 2.17 M，几乎与作为阳性对照的酮康唑相当。决明子叶乙醇提取物和乙酸乙酯提取物的 MIC 测试结果显示，乙醇提取物的 MIC 为 100 ppm，乙酸乙酯提取物的 MIC 为 50 ppm。这一结果得到了 FE-SEM 结果的支持，FE-SEM 结果表明，100 ppm 的乙醇提取物可破坏白色念珠菌菌落的结构。
{"title":"In vitro and In silico Studies of Kayu Raja (Cassia fistula L.) Leaves Extract as Potential Antifungal Agent Against Candida albicans","authors":"Tan David Christian, K. Kasiyati, Tri Yuliani, Ariyanti Saputri, Dadang Priyoatmojo, Marrisa Angelina","doi":"10.14710/jksa.26.9.344-352","DOIUrl":"https://doi.org/10.14710/jksa.26.9.344-352","url":null,"abstract":"Candida albicans is one of the most common fungal species causing opportunistic infections, such as candidiasis. Candida albicans has the ability to produce and secrete hydrolytic enzymes, namely secrete aspartate protease (SAP). SAP3 is a virulence factor for mucosal or disseminated infections. Cassia fistula leaves have bioactive compounds that can be used as antimicrobial agents, such as hyperoside, delphin, epicatechin, isoquercitrin, and astragalin. This study aims to determine the potential of bioactive compounds in Cassia fistula L. as an antifungal by in silico method molecular docking and Minimum Inhibitory Concentration (MIC) analysis with FE-SEM test for microscopical visual results. The results showed that the delphin compound had the best binding energy of -7.73 and an inhibition constant of 2.17 M, almost equivalent to ketoconazole as a positive control. MIC test of ethanol and ethyl acetate extracts of Cassia fistula leaves resulted in 100 ppm in the ethanol extract and 50 ppm in the ethyl acetate fraction. This result was supported by FE-SEM results, which showed that the ethanol extract at 100 ppm could damage the structure of Candida albicans colony.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139235552","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-24DOI: 10.14710/jksa.26.9.332-343
Liqanatul Putri Sholikah, S. Sumari, Yuneta Dwi Yunisari
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.
{"title":"Modification and Application Study of Activated Natural Zeolite for the Treatment of Liquid Waste from Chemical Laboratory","authors":"Liqanatul Putri Sholikah, S. Sumari, Yuneta Dwi Yunisari","doi":"10.14710/jksa.26.9.332-343","DOIUrl":"https://doi.org/10.14710/jksa.26.9.332-343","url":null,"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.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"47 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139239944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The Lawson dye contained in the leaves of Lawsonia inermis L. has a red-orange color, which can be used as a fabric dye. The solvent is ethanol because it can attract flavonoid compounds bound to Lawson. The ultrasonic-assisted extraction method is employed to enhance the extraction process by breaking down cell walls, thereby facilitating a more rapid extraction of the desired solute. This study investigated the effects of material-to-solvent ratio, ethanol concentration, and extraction time. The research results were analyzed using a UV-Visible spectrophotometer to determine the yield of Lawson extract. The Face-Centered Composite Design (FCCCD) method was applied to this study to obtain optimal analysis results and extraction conditions. The independent variables in this study were the ratio of ingredients to solvent (0.02-0.06 g/g), ethanol concentration (20-60%), and extraction time (5-15 minutes). The optimal extraction conditions were obtained at a ratio of 0.02 g/g, an ethanol concentration of 60%, and an extraction time of 15 minutes, with a predicted model yield of 15.417%. The actual yield under these conditions was found to be 15.4934%. Furthermore, the extraction kinetics model was analyzed to study and predict the optimal Lawson extraction results. Extraction kinetics calculations were carried out using first-order and second-order based on the Lagergren equation. The most suitable extraction kinetic model is second-order with a determinant coefficient value, or the value of R2 is 1, which indicates that the order kinetic model equation represents the actual conditions.
{"title":"Optimization and Kinetics Extraction of Natural Dyes from Henna Leaves (Lawsonia inermis L.) with Ultrasonic Assistance","authors":"Achmad Qodim Syafaatullah, Dwi Setyorini, Melani Ganing, Renova Panjaitan, Ni’matul Azizah","doi":"10.14710/jksa.26.9.324-331","DOIUrl":"https://doi.org/10.14710/jksa.26.9.324-331","url":null,"abstract":"The Lawson dye contained in the leaves of Lawsonia inermis L. has a red-orange color, which can be used as a fabric dye. The solvent is ethanol because it can attract flavonoid compounds bound to Lawson. The ultrasonic-assisted extraction method is employed to enhance the extraction process by breaking down cell walls, thereby facilitating a more rapid extraction of the desired solute. This study investigated the effects of material-to-solvent ratio, ethanol concentration, and extraction time. The research results were analyzed using a UV-Visible spectrophotometer to determine the yield of Lawson extract. The Face-Centered Composite Design (FCCCD) method was applied to this study to obtain optimal analysis results and extraction conditions. The independent variables in this study were the ratio of ingredients to solvent (0.02-0.06 g/g), ethanol concentration (20-60%), and extraction time (5-15 minutes). The optimal extraction conditions were obtained at a ratio of 0.02 g/g, an ethanol concentration of 60%, and an extraction time of 15 minutes, with a predicted model yield of 15.417%. The actual yield under these conditions was found to be 15.4934%. Furthermore, the extraction kinetics model was analyzed to study and predict the optimal Lawson extraction results. Extraction kinetics calculations were carried out using first-order and second-order based on the Lagergren equation. The most suitable extraction kinetic model is second-order with a determinant coefficient value, or the value of R2 is 1, which indicates that the order kinetic model equation represents the actual conditions.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"939 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139248816","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-11-14DOI: 10.14710/jksa.26.8.318-323
J. Al-Anshori, Ajar Faflul Abror, Juliandri Juliandri, Agus Safari, A. Hidayat
The chemosensor selectivity of 3-oxo-3H-benzo[f]chromen-2-carboxylic acid (ABKK) toward Na+ metal ionhas been successfully studied in silico using FMO (Frontier Molecular Orbital) analysis method. The geometry of the ABKK structure was optimized by the DFT (Density Functional Theory) method with a function/basis set: M06/6-31G (d, p). Afterward, the electronic properties of the ABKK structure before and after binding to sodium ion were analyzed and compared with the ABKK+other metal ion structures representing valence charges 1-3 and within the constraints of the basis set used. The results of geometry optimization showed that 1ABKK+Na+ has a more positive frequency/minima than 2ABKK+Na+ with interaction energies of 145 and 200.5 kcal/mol, respectively. Ignoring the role of solvents, FMO analysis revealed that the bandgap energy of fluorophore and receptor interactions (∆E LUMO Fl-Rs 1ABKK+Na+) and (∆E HOMO Fl-Rs 2ABKK+Na+) were 0.631 and 0.336 eV, correspondingly. In addition, the bandgap energy of fluorophore/∆E Fl 1ABKK+Na+ and 2ABKK+Na+ were calculated at 4.347 and 4.362 eV. Comparing those two types of bandgap energies with the bandgap belonging to ABKK+other metal ions, the excitation, and PET (Photoinduced Electron Transfer) processes were estimated to be relatively favorable experienced by 2ABKK+Na+. Finally, the selectivity of ABKK toward sodium metal ions from the computational calculations was relatively in agreement with the laboratory experimental results.
{"title":"In Silico DFT (Density Functional Theory) Study of Chemosensor Selectivity of 3-Oxo-3H-Benzo[f]chromen-2-Carboxylic Acid (ABKK) on Sodium Metal Ion Using FMO (Frontier Molecular Orbital) Analysis","authors":"J. Al-Anshori, Ajar Faflul Abror, Juliandri Juliandri, Agus Safari, A. Hidayat","doi":"10.14710/jksa.26.8.318-323","DOIUrl":"https://doi.org/10.14710/jksa.26.8.318-323","url":null,"abstract":"The chemosensor selectivity of 3-oxo-3H-benzo[f]chromen-2-carboxylic acid (ABKK) toward Na+ metal ionhas been successfully studied in silico using FMO (Frontier Molecular Orbital) analysis method. The geometry of the ABKK structure was optimized by the DFT (Density Functional Theory) method with a function/basis set: M06/6-31G (d, p). Afterward, the electronic properties of the ABKK structure before and after binding to sodium ion were analyzed and compared with the ABKK+other metal ion structures representing valence charges 1-3 and within the constraints of the basis set used. The results of geometry optimization showed that 1ABKK+Na+ has a more positive frequency/minima than 2ABKK+Na+ with interaction energies of 145 and 200.5 kcal/mol, respectively. Ignoring the role of solvents, FMO analysis revealed that the bandgap energy of fluorophore and receptor interactions (∆E LUMO Fl-Rs 1ABKK+Na+) and (∆E HOMO Fl-Rs 2ABKK+Na+) were 0.631 and 0.336 eV, correspondingly. In addition, the bandgap energy of fluorophore/∆E Fl 1ABKK+Na+ and 2ABKK+Na+ were calculated at 4.347 and 4.362 eV. Comparing those two types of bandgap energies with the bandgap belonging to ABKK+other metal ions, the excitation, and PET (Photoinduced Electron Transfer) processes were estimated to be relatively favorable experienced by 2ABKK+Na+. Finally, the selectivity of ABKK toward sodium metal ions from the computational calculations was relatively in agreement with the laboratory experimental results.","PeriodicalId":17811,"journal":{"name":"Jurnal Kimia Sains dan Aplikasi","volume":"29 12","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139277064","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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