Pub Date : 2023-07-06DOI: 10.26554/sti.2023.8.3.361-366
Novianty Novianty, J. Edianta, Jorena Jorena, Khairul Saleh, A. Bama, E. Koriyanti, M. Ariani, I. Royani
This study was conducted to synthesize Fe (III)-IIPs by free radical polymerization using the cooling-heating method. Cooling processat -5◦C for 1 hour, as well as heating at 75◦C, 80◦C, and 85◦C maintained for 3 hours, 2 hours and 1 hour, respectively. The Fe (III)-IIPs synthesis process involved Fe(NO3)3 with an average diameter of 18.23 nm, methacrylic acid (MAA), ethylene glycol dimethacrylate (EGDMA), benzoyl peroxide (BPO) and ethanol, each of which plays a role as an analyte, functional monomer, cross-linker, initiator, and porogen. The result of the polymerization process was a polymer containing ions namely Fe(III) polymer. The ions need to be removed by the extraction process to produce Fe(III)-IIPs, which act as absorbents. Furthermore, the extraction process is very influential in the process of losing ions and the formation of cavities or templates in the polymer body. The number of cavities formed tends to affect the ability of Fe(III)-IIPs to identify the target ion which has similar physical and chemical properties to the shape of the Fe(III)-IIPs cavity. The extraction process was carried out on Fe(III) polymer samples using HCl and HNO3 solutions with varying concentrations of 3 M and 6 M, respectively. The transmission percentage of FTIR analysis showed that for samples of Fe(III)-IIPs HCl 3 M and 6 M were 94.258% and 95.666%, while for Fe(III)-IIPs HNO3 3 M and 6 M were 92.735%, respectively. The largest percentage was shown in the 6 M HCl IIPs sample, which indicated that there were several ions lost from the polymer body after the extraction process. This is also reinforced by the results of the SEM analysis processed with Matlab, which showed 498 cavities with a distribution of voids on a scale of <100 nm, totaling 470.
{"title":"Synthesis of Fe(III)-IIPs (Ion Imprinted Polymers): Comparing Different Concentrations of HCl and HNO3 Solutions in the Fe(III) Polymer Extraction Process for Obtaining the Largest Cavities in Fe(III)-IIPs","authors":"Novianty Novianty, J. Edianta, Jorena Jorena, Khairul Saleh, A. Bama, E. Koriyanti, M. Ariani, I. Royani","doi":"10.26554/sti.2023.8.3.361-366","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.361-366","url":null,"abstract":"This study was conducted to synthesize Fe (III)-IIPs by free radical polymerization using the cooling-heating method. Cooling processat -5◦C for 1 hour, as well as heating at 75◦C, 80◦C, and 85◦C maintained for 3 hours, 2 hours and 1 hour, respectively. The Fe (III)-IIPs synthesis process involved Fe(NO3)3 with an average diameter of 18.23 nm, methacrylic acid (MAA), ethylene glycol dimethacrylate (EGDMA), benzoyl peroxide (BPO) and ethanol, each of which plays a role as an analyte, functional monomer, cross-linker, initiator, and porogen. The result of the polymerization process was a polymer containing ions namely Fe(III) polymer. The ions need to be removed by the extraction process to produce Fe(III)-IIPs, which act as absorbents. Furthermore, the extraction process is very influential in the process of losing ions and the formation of cavities or templates in the polymer body. The number of cavities formed tends to affect the ability of Fe(III)-IIPs to identify the target ion which has similar physical and chemical properties to the shape of the Fe(III)-IIPs cavity. The extraction process was carried out on Fe(III) polymer samples using HCl and HNO3 solutions with varying concentrations of 3 M and 6 M, respectively. The transmission percentage of FTIR analysis showed that for samples of Fe(III)-IIPs HCl 3 M and 6 M were 94.258% and 95.666%, while for Fe(III)-IIPs HNO3 3 M and 6 M were 92.735%, respectively. The largest percentage was shown in the 6 M HCl IIPs sample, which indicated that there were several ions lost from the polymer body after the extraction process. This is also reinforced by the results of the SEM analysis processed with Matlab, which showed 498 cavities with a distribution of voids on a scale of <100 nm, totaling 470.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44154783","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.353-360
B. D. Afrah, M. Riady, L. Cundari, Muhammad Andzar Rizan, Jihan Utami, Siti Istiani Pratiwi, M. Y. Pratama
A large amount of rubberwood waste in Indonesia is caused by abundant rubberwood production. However, the utilization of rubberwood waste has not been optimized in Indonesia. One of the efforts to utilize rubberwood waste is to process it into liquid smoke. Liquid smoke is the dispersion of smoke vapor in water. The raw material used in this research is rubberwood. This study aimed to determine the quality of liquid smoke after purification by knowing the volume, density, pH, viscosity, yield, and phenol content using rubberwood as raw material and the pyrolysis method. The pyrolysis process is purified by distillation based on differences in boiling points. This research is divided into two stages of distillation, namely low grade purified liquid smoke and high grade purified liquid smoke. The analysis results will follow the quality standards of Japanese liquid smoke. The results show that the best liquid smoke from this research is liquid smoke with a pyrolysis time of 3 hours because it meets Japanese liquid smoke quality standards.
{"title":"Optimization of Liquid Smoke Products Made from Rubberwood with Pyrolysis Method","authors":"B. D. Afrah, M. Riady, L. Cundari, Muhammad Andzar Rizan, Jihan Utami, Siti Istiani Pratiwi, M. Y. Pratama","doi":"10.26554/sti.2023.8.3.353-360","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.353-360","url":null,"abstract":"A large amount of rubberwood waste in Indonesia is caused by abundant rubberwood production. However, the utilization of rubberwood waste has not been optimized in Indonesia. One of the efforts to utilize rubberwood waste is to process it into liquid smoke. Liquid smoke is the dispersion of smoke vapor in water. The raw material used in this research is rubberwood. This study aimed to determine the quality of liquid smoke after purification by knowing the volume, density, pH, viscosity, yield, and phenol content using rubberwood as raw material and the pyrolysis method. The pyrolysis process is purified by distillation based on differences in boiling points. This research is divided into two stages of distillation, namely low grade purified liquid smoke and high grade purified liquid smoke. The analysis results will follow the quality standards of Japanese liquid smoke. The results show that the best liquid smoke from this research is liquid smoke with a pyrolysis time of 3 hours because it meets Japanese liquid smoke quality standards.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46379081","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.338-343
E. Q. Jasim
Mesalazine, often referred to as mesalamine or 5-aminosalicylic acid (5-ASA), and its derivatives are some of the first medications to be approved for treating digestive tract inflammations, including ulcerative colitis and mild to moderate Crohn’s disease. Sulfasalazine, discovered in 1938 for therapeutic use, was the first mesalazine derivative. High yields of four different mesalazine derivatives were synthesized, including two Schiff bases and two azo compounds. The present study involved the synthesis of Schiff bases through the reaction of mesalazine with pyrrole-2-carbaldehyde or indole-2-carbaldehyde, resulting in the formation of 5-(((1H-pyrrol-2-yl)methylene)amino)-2-hydroxybenzoic acid (1) or 5-(((1H-indol-2-yl)methylene)amino)-2hydroxybenzoic acid (2), respectively. The synthesis of azo compounds involved the coupling of mesalazine with sulfamethoxazole or pyridoxine, resulting in the formation of 5-amino-2-hydroxy-3-((4-(N-(5-methylisoxazol-3-yl)sulfamoyl)phenyl)diazenyl)benzoic acid (3) or 2-hydroxy-5-((5-hydroxy-3,4-bis(hydroxymethyl)-6-methylpyridin-2-yl)diazenyl)benzoic acid (4), respectively. The identification of the synthesized compounds was carried out using IR and 1H-NMR spectroscopy. Antibacterial assessment of the synthetic compounds was performed in vitro against gram-negative bacteria (such as Escherichia coli and Pseudomonas aeruginosa) and gram-positive bacteria (Staphylococcus aureus). The antibacterial activity studies demonstrated that against Escherichia coli and Staphylococcus aureus, the Schiff base compounds are more active than azo compounds. Compound 1 showed the highest activity, resulting in a 23 mm inhibition zone against E. coli at 1000 ug/ml. In contrast, the antibacterial activity of compound 2 was observed to be 25 mm against S. aureus at the same highest concentration.
{"title":"Synthesis, Characterization, and Antibacterial Activity of Some Mesalazine Derivatives","authors":"E. Q. Jasim","doi":"10.26554/sti.2023.8.3.338-343","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.338-343","url":null,"abstract":"Mesalazine, often referred to as mesalamine or 5-aminosalicylic acid (5-ASA), and its derivatives are some of the first medications to be approved for treating digestive tract inflammations, including ulcerative colitis and mild to moderate Crohn’s disease. Sulfasalazine, discovered in 1938 for therapeutic use, was the first mesalazine derivative. High yields of four different mesalazine derivatives were synthesized, including two Schiff bases and two azo compounds. The present study involved the synthesis of Schiff bases through the reaction of mesalazine with pyrrole-2-carbaldehyde or indole-2-carbaldehyde, resulting in the formation of 5-(((1H-pyrrol-2-yl)methylene)amino)-2-hydroxybenzoic acid (1) or 5-(((1H-indol-2-yl)methylene)amino)-2hydroxybenzoic acid (2), respectively. The synthesis of azo compounds involved the coupling of mesalazine with sulfamethoxazole or pyridoxine, resulting in the formation of 5-amino-2-hydroxy-3-((4-(N-(5-methylisoxazol-3-yl)sulfamoyl)phenyl)diazenyl)benzoic acid (3) or 2-hydroxy-5-((5-hydroxy-3,4-bis(hydroxymethyl)-6-methylpyridin-2-yl)diazenyl)benzoic acid (4), respectively. The identification of the synthesized compounds was carried out using IR and 1H-NMR spectroscopy. Antibacterial assessment of the synthetic compounds was performed in vitro against gram-negative bacteria (such as Escherichia coli and Pseudomonas aeruginosa) and gram-positive bacteria (Staphylococcus aureus). The antibacterial activity studies demonstrated that against Escherichia coli and Staphylococcus aureus, the Schiff base compounds are more active than azo compounds. Compound 1 showed the highest activity, resulting in a 23 mm inhibition zone against E. coli at 1000 ug/ml. In contrast, the antibacterial activity of compound 2 was observed to be 25 mm against S. aureus at the same highest concentration.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46306307","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.403-413
H. Akhsan, Muhammad Irfan, Supari Supari, I. Iskandar
This article examines the extreme climate events on the Eastern Coast of Sumatra over four decades (1981-2019) based on the extreme rainfall index defined using the Expert Team on Climate Change Detection and Indices (ETCCDI). The indices used include Consecutive Dry Day (CDD and the total rainfall per year (PRCPTOT). Theses indices were calculated and are based on the daily observation data from eight quality-controlled weather stations. While overall trends in extreme rainfall indices are not significant, there is a noticeable trend towards drought, with CDD rising by 1.23 days per decade and PRCPTOT decreased by 3.16 mm/year. The correlation between the Dipole Mode Index (DMI) and extreme rainfall indices in the August-September-October-November (ASON) period was positive, with CDD increasing with the more positive DMI value. On the other hand, the PRCPTOT index showed a decrease as the DMI more positive. The ENSO index and CDD are positively correlated during the dry season, while ENSO index negatively correlates with PRCPTOT. The duration of CDD during El Niño/positive Indian Ocean Dipole (IOD) events in 1997, 2015, and 2019 had significant impact on the forest and land fires on the Eastern Coast of Sumatra. The results are useful for policymakers in preventing forest and land fires on the Eastern Coast of Sumatra.
{"title":"Dynamics of Extreme Rainfall and Its Impact on Forest and Land Fires in the Eastern Coast of Sumatra","authors":"H. Akhsan, Muhammad Irfan, Supari Supari, I. Iskandar","doi":"10.26554/sti.2023.8.3.403-413","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.403-413","url":null,"abstract":"This article examines the extreme climate events on the Eastern Coast of Sumatra over four decades (1981-2019) based on the extreme rainfall index defined using the Expert Team on Climate Change Detection and Indices (ETCCDI). The indices used include Consecutive Dry Day (CDD and the total rainfall per year (PRCPTOT). Theses indices were calculated and are based on the daily observation data from eight quality-controlled weather stations. While overall trends in extreme rainfall indices are not significant, there is a noticeable trend towards drought, with CDD rising by 1.23 days per decade and PRCPTOT decreased by 3.16 mm/year. The correlation between the Dipole Mode Index (DMI) and extreme rainfall indices in the August-September-October-November (ASON) period was positive, with CDD increasing with the more positive DMI value. On the other hand, the PRCPTOT index showed a decrease as the DMI more positive. The ENSO index and CDD are positively correlated during the dry season, while ENSO index negatively correlates with PRCPTOT. The duration of CDD during El Niño/positive Indian Ocean Dipole (IOD) events in 1997, 2015, and 2019 had significant impact on the forest and land fires on the Eastern Coast of Sumatra. The results are useful for policymakers in preventing forest and land fires on the Eastern Coast of Sumatra.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47608405","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.471-478
S. J. Kadhem
Alumina thin films have significant applications in the areas of optoelectronics, optics, electrical insulators, sensors and tribology. The novel aspect of this work is that the homogeneous alumina thin films were prepared in several stages to generate a plasma jet. In this paper, aluminium nanoparticles suspended in vinyl alcohol were prepared using exploding wire plasma. TEM analysis was used to determine the size and shape of particles in aluminium and vinyl alcohol suspensions; the TEM images showed that the particle size is 17.2 nm. Aluminium/poly vinyl alcohol (Al/PVA) thin films were prepared using this suspension on quartz substrate by plasma jet technique at room temperature with an argon gas flow rate of 1 L/min. The Al/PVA thin films were thermally converted to alumina films, where they were annealed at different temperatures (700, 800, or 900°C). X-ray diffraction (XRD), atomic force microscopy (AFM), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR) techniques were used to characterise these thin films before and after annealing process. The diffraction patterns of the prepared thin films before subjecting them to the annealing process indicated the presence of peaks belonging to aluminium and PVA; however, the diffraction patterns and FTIR spectra obtained for these films after the annealing process showed peaks indicating the formation of alumina films of different phases. AFM and SEM investigations proved that the formed particles for all prepared films before and after the annealing process were similar in size and almost spherical; the diameter of the particles was on the order of a few nanometres. To control the properties of prepared thin films, the plasma which was used to produce thin films is diagnosed spectrophotometrically. The generated plasma was diagnosed using optical emission spectroscopy to estimate the electron temperature Te; the electron temperature was 1.925 eV.
{"title":"Preparation of Al2O3 /PVA Nanocomposite Thin Films by a Plasma Jet Method","authors":"S. J. Kadhem","doi":"10.26554/sti.2023.8.3.471-478","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.471-478","url":null,"abstract":"Alumina thin films have significant applications in the areas of optoelectronics, optics, electrical insulators, sensors and tribology. The novel aspect of this work is that the homogeneous alumina thin films were prepared in several stages to generate a plasma jet. In this paper, aluminium nanoparticles suspended in vinyl alcohol were prepared using exploding wire plasma. TEM analysis was used to determine the size and shape of particles in aluminium and vinyl alcohol suspensions; the TEM images showed that the particle size is 17.2 nm. Aluminium/poly vinyl alcohol (Al/PVA) thin films were prepared using this suspension on quartz substrate by plasma jet technique at room temperature with an argon gas flow rate of 1 L/min. The Al/PVA thin films were thermally converted to alumina films, where they were annealed at different temperatures (700, 800, or 900°C). X-ray diffraction (XRD), atomic force microscopy (AFM), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR) techniques were used to characterise these thin films before and after annealing process. The diffraction patterns of the prepared thin films before subjecting them to the annealing process indicated the presence of peaks belonging to aluminium and PVA; however, the diffraction patterns and FTIR spectra obtained for these films after the annealing process showed peaks indicating the formation of alumina films of different phases. AFM and SEM investigations proved that the formed particles for all prepared films before and after the annealing process were similar in size and almost spherical; the diameter of the particles was on the order of a few nanometres. To control the properties of prepared thin films, the plasma which was used to produce thin films is diagnosed spectrophotometrically. The generated plasma was diagnosed using optical emission spectroscopy to estimate the electron temperature Te; the electron temperature was 1.925 eV.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49114970","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.388-396
O. V. Eboy, Ricky Anak Kemarau
Weather and climate in Malaysia, situated in Southeast Asia, are influenced by El Niño Southern Oscillation (ENSO), monsoons, Madden Julian Oscillation (MJO), and Indian Ocean Dipole (IOD). Previous studies on ENSO’s impact on temperature lacked detailed spatial information due to limited meteorological stations and cost constraints. This study utilizes remote sensing techniques, employing Landsat satellite data and Oceanic Niño Index (ONI) data, to analyze the spatial pattern of extreme land surface temperature distribution during ENSO events. Preprocessing includes radiometric and atmospheric corrections before converting digital numbers to land surface temperature values. Results indicate increased hotspot areas (>30°C) during El Niño events, with respective hotspot areas of 89.32 km² and 97.8 km² in 2015 and 2016, and 61.23 km² and 59.73 km² during La Niña in August and October 2018. Heat concentration areas remained consistent during the 1998 El Niño (89.32 km²) and the 2011 La Niña (55.82 km²). These findings highlight ENSO’s influence on altering hotspot distribution patterns. The increased hotspot area during El Niño events (34-36 km²) led to a 20-30% surge in electricity consumption as residents and offices in Kuching City, Sarawak, sought temperature regulation. This spatial information aids the government in identifying affected areas and implementing suitable measures to mitigate the impact of El Niño events.
{"title":"Analysis of Extreme Heat Land Surface Temperature at a Tropical City (1988-2022): A Study on the Variability of Hot Spot during El Niño Southern Oscillation (ENSO)","authors":"O. V. Eboy, Ricky Anak Kemarau","doi":"10.26554/sti.2023.8.3.388-396","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.388-396","url":null,"abstract":"Weather and climate in Malaysia, situated in Southeast Asia, are influenced by El Niño Southern Oscillation (ENSO), monsoons, Madden Julian Oscillation (MJO), and Indian Ocean Dipole (IOD). Previous studies on ENSO’s impact on temperature lacked detailed spatial information due to limited meteorological stations and cost constraints. This study utilizes remote sensing techniques, employing Landsat satellite data and Oceanic Niño Index (ONI) data, to analyze the spatial pattern of extreme land surface temperature distribution during ENSO events. Preprocessing includes radiometric and atmospheric corrections before converting digital numbers to land surface temperature values. Results indicate increased hotspot areas (>30°C) during El Niño events, with respective hotspot areas of 89.32 km² and 97.8 km² in 2015 and 2016, and 61.23 km² and 59.73 km² during La Niña in August and October 2018. Heat concentration areas remained consistent during the 1998 El Niño (89.32 km²) and the 2011 La Niña (55.82 km²). These findings highlight ENSO’s influence on altering hotspot distribution patterns. The increased hotspot area during El Niño events (34-36 km²) led to a 20-30% surge in electricity consumption as residents and offices in Kuching City, Sarawak, sought temperature regulation. This spatial information aids the government in identifying affected areas and implementing suitable measures to mitigate the impact of El Niño events.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"68995031","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.436-442
A. Janteng, Desmond Lee Ching Yiing, Yongkui Lun, Jaludin Janteng, Lee See Keong, R. Omar, Andy Liew Pik Hern
In this article, we represent A as the of analytic functions in the open unit disk. Further, new subclasses of analytic functions of complex order utilising q-derivative operator are generated. The subclasses are symbolised by Hq,b(ϕ) and Iq,b(ϕ). Additionally, we discover that these function classes are implicated with the Fekete-Szegö inequalities.
{"title":"The Subclasses of Analytic Functions of Complex Order with Application of q-Derivative Operators","authors":"A. Janteng, Desmond Lee Ching Yiing, Yongkui Lun, Jaludin Janteng, Lee See Keong, R. Omar, Andy Liew Pik Hern","doi":"10.26554/sti.2023.8.3.436-442","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.436-442","url":null,"abstract":"In this article, we represent A as the of analytic functions in the open unit disk. Further, new subclasses of analytic functions of complex order utilising q-derivative operator are generated. The subclasses are symbolised by Hq,b(ϕ) and Iq,b(ϕ). Additionally, we discover that these function classes are implicated with the Fekete-Szegö inequalities.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45445147","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.414-421
R. Mohadi, N. Palapa, Sahrul Wibiyan, M. Mardiyanto, Rohmatullaili Rohmatullaili, Erni Salasia Fitri, A. Lesbani
In this study, composite layer double hydroxide-metal oxide catalysts (Ni/Al-TiO2 and Ni/Al-ZnO) were successfully prepared and utilized for the oxidative desulfurization of dibenzothiophene. The catalysts were characterized using XRD, FTIR, and SEM-EDS analysis. The diffraction patterns confirmed the successful synthesis of the composite materials, while the FTIR spectra exhibited absorption bands at specific wavenumbers 3480 cm-1, 1630 cm-1, 1376 cm-1, 830 cm-1, 775 cm-1, and 683 cm-1. The surface morphology of the catalysts showed variations, with Ni/Al-LDH having a smooth particle surface and long particle shape, while Ni/Al-ZnO and Ni/Al-TiO2 formed grain-like or aggregated structures. EDS analysis confirmed the presence of Ni/Al, Ti, and Zn elements in the composites, with Ti and Zn accounting for 29.3% and 10.7% of the composite mass, respectively. The optimized reaction conditions included a reaction time of 40 minutes, catalyst dosage of 0.25 g, temperature of 50°C, and the use of n-hexane as the solvent. The catalysts demonstrated a heterogeneous nature and proved to be reusable, as the conversion of dibenzothiophene remained above 90% even after three catalytic reactions, with Ni/Al-TiO2 and Ni/Al-ZnO composites maintaining conversion rates of 99.36% and 99.32%, respectively.
{"title":"Catalytic Oxidative Desulfurization of 4-Methyldibenzothiophene by Ni/Al Modified Titanium Dioxide and Zinc Oxide","authors":"R. Mohadi, N. Palapa, Sahrul Wibiyan, M. Mardiyanto, Rohmatullaili Rohmatullaili, Erni Salasia Fitri, A. Lesbani","doi":"10.26554/sti.2023.8.3.414-421","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.414-421","url":null,"abstract":"In this study, composite layer double hydroxide-metal oxide catalysts (Ni/Al-TiO2 and Ni/Al-ZnO) were successfully prepared and utilized for the oxidative desulfurization of dibenzothiophene. The catalysts were characterized using XRD, FTIR, and SEM-EDS analysis. The diffraction patterns confirmed the successful synthesis of the composite materials, while the FTIR spectra exhibited absorption bands at specific wavenumbers 3480 cm-1, 1630 cm-1, 1376 cm-1, 830 cm-1, 775 cm-1, and 683 cm-1. The surface morphology of the catalysts showed variations, with Ni/Al-LDH having a smooth particle surface and long particle shape, while Ni/Al-ZnO and Ni/Al-TiO2 formed grain-like or aggregated structures. EDS analysis confirmed the presence of Ni/Al, Ti, and Zn elements in the composites, with Ti and Zn accounting for 29.3% and 10.7% of the composite mass, respectively. The optimized reaction conditions included a reaction time of 40 minutes, catalyst dosage of 0.25 g, temperature of 50°C, and the use of n-hexane as the solvent. The catalysts demonstrated a heterogeneous nature and proved to be reusable, as the conversion of dibenzothiophene remained above 90% even after three catalytic reactions, with Ni/Al-TiO2 and Ni/Al-ZnO composites maintaining conversion rates of 99.36% and 99.32%, respectively.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41377731","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.501-508
Yudi Wicaksono, Kuni Zu’aimah Barikah, Amanda Della Yudatama, Havidhatul Maulia, N. Nuri, D. Setyawan
Curcumin (CUR) is a polyphenolic compound that exhibits potent anti-inflammatory activity. However, only a tiny amount of CUR is absorbed during oral administration, which is because CUR is difficult to dissolve in water. The aim of the research was to increase the solubility of CUR through the cocrystallization technique using isonicotinamide coformer (INIC) by solvent evaporation. Cocrystal characterization was carried out using a powder X-ray diffractometer (PXRD), a differential scanning calorimeter (DSC), a Fourier transform infrared spectrometer (FTIR), and a scanning electron microscope (SEM). Solubility was evaluated using the shaking method, while the anti-inflammatory activity test was carried out using the carrageenan induced mouse leg edema method. The resulting CUR-INIC (1:1) cocrystal has a diffractogram with new diffraction peaks of 2theta at 15.00, 16.22, and 22.89◦ compared to the individual diffractograms of CUR and INIC. In the cocrystal, CUR and INIC form intermolecular interactions of hydrogen bonds, resulting in a new solid phase with a melting point of 160.1◦C. The solubility of the CUR-INIC cocrystal in water was 73.1±0.23 ug/mL, which increased 14 times compared to the solubility of initial CUR, which was only 5.05±0.07 ug/mL. The CUR-INIC cocrystal showed a percentage of edema inhibition in mice (5 hours) 130% more potent than that of initial CUR. Therefore, CUR-INIC cocrystals can be used to improve CUR solubility to obtain more excellent anti-inflammatory effects.
{"title":"Increasing the Solubility and Anti-Inflammatory Activity of Curcumin by Cocrystallization","authors":"Yudi Wicaksono, Kuni Zu’aimah Barikah, Amanda Della Yudatama, Havidhatul Maulia, N. Nuri, D. Setyawan","doi":"10.26554/sti.2023.8.3.501-508","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.501-508","url":null,"abstract":"Curcumin (CUR) is a polyphenolic compound that exhibits potent anti-inflammatory activity. However, only a tiny amount of CUR is absorbed during oral administration, which is because CUR is difficult to dissolve in water. The aim of the research was to increase the solubility of CUR through the cocrystallization technique using isonicotinamide coformer (INIC) by solvent evaporation. Cocrystal characterization was carried out using a powder X-ray diffractometer (PXRD), a differential scanning calorimeter (DSC), a Fourier transform infrared spectrometer (FTIR), and a scanning electron microscope (SEM). Solubility was evaluated using the shaking method, while the anti-inflammatory activity test was carried out using the carrageenan induced mouse leg edema method. The resulting CUR-INIC (1:1) cocrystal has a diffractogram with new diffraction peaks of 2theta at 15.00, 16.22, and 22.89◦ compared to the individual diffractograms of CUR and INIC. In the cocrystal, CUR and INIC form intermolecular interactions of hydrogen bonds, resulting in a new solid phase with a melting point of 160.1◦C. The solubility of the CUR-INIC cocrystal in water was 73.1±0.23 ug/mL, which increased 14 times compared to the solubility of initial CUR, which was only 5.05±0.07 ug/mL. The CUR-INIC cocrystal showed a percentage of edema inhibition in mice (5 hours) 130% more potent than that of initial CUR. Therefore, CUR-INIC cocrystals can be used to improve CUR solubility to obtain more excellent anti-inflammatory effects.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46237939","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 : 2023-07-06DOI: 10.26554/sti.2023.8.3.451-460
Soraya Aulia, R. Primaharinastiti, D. Purwanto
This paper explains the development of a quick and easy gas chromatography (GC) approach to identify methamphetamine in urine. This research used gas chromatography with mass spectroscopy and a capillary column TG-5SILMS (5% phenyl methyl siloxane, 30 m x 0.32 x 25 m). The carrier gas flow rate was set at 1.0 mL/minute, the temperature inlet and detector had been set at 300°C, and the oven temperature was programmed to initiate at 50°C and held for 1.5 minutes before being raised to 300°C at a rate 40°C/minute and held for 3 minutes. Sample pre-treatment by modification of the QuEChERS method includes using a relatively large amount of inorganic salt, extraction volume and extraction cycle. The optimal conditions for processing a 400 uL urine sample were 160 mg magnesium sulphate, 40 mg sodium chloride, and 400 uL acetonitrile for organic solvent. According to the validation test, the detection limit for methamphetamine was 0.36 ug/mL; the quantitation limit was 1.09 ug/mL, and the calibration curve followed the regression line. y=1.0489x-3.7914, coefficient (r) was 0.9973. The recovery of the analyte spiked into urine at 5, 7 and 9 ug/mL on average was 100.5±2.33% for intraday dan 93.3±7.21% for interday. The precision was excellent, with an average coefficient of variation of 2.31%. The procedure was applied to four urine samples from drug users and the first abuser (25.51 ug/mL), the second abuser (15.05 ug/mL), the third abuser (17.72 ug/mL) and the last abuser (3.08 ug/mL) were all satisfactorily quantitated.
本文介绍了一种快速简便的气相色谱法（GC）检测尿液中甲基苯丙胺的方法。本研究使用了气相色谱质谱和毛细管柱TG-5SILMS（5%苯基甲基硅氧烷，30m x 0.32 x 25m）。载气流速设定为1.0 mL/分钟，温度入口和检测器设定为300°C，烘箱温度设定为在50°C启动并保持1.5分钟，然后以40°C/分钟的速度升至300°C并保持3分钟。通过改进QuEChERS方法对样品进行预处理，包括使用相对大量的无机盐、提取体积和提取周期。处理400微升尿样的最佳条件是160毫克硫酸镁、40毫克氯化钠和400微升乙腈作为有机溶剂。根据验证试验，甲基苯丙胺的检测限为0.36微克/毫升；定量限为1.09ug/mL，校准曲线遵循回归线。y=1.0489x-3.7914，系数（r）为0.9973。以5、7和9微克/毫升的浓度掺入尿液的分析物的平均回收率为100.5±2.33%，日间为93.3±7.21%。该程序应用于吸毒者的四份尿液样本，第一次吸毒者（25.51微克/毫升）、第二次吸毒者、第三次吸毒者和最后一次吸毒者的尿液样本均能令人满意地定量。
{"title":"Development and Validation GC/MS Method for Methamphetamine Analysis in Urine by Miniaturization QuEChERS","authors":"Soraya Aulia, R. Primaharinastiti, D. Purwanto","doi":"10.26554/sti.2023.8.3.451-460","DOIUrl":"https://doi.org/10.26554/sti.2023.8.3.451-460","url":null,"abstract":"This paper explains the development of a quick and easy gas chromatography (GC) approach to identify methamphetamine in urine. This research used gas chromatography with mass spectroscopy and a capillary column TG-5SILMS (5% phenyl methyl siloxane, 30 m x 0.32 x 25 m). The carrier gas flow rate was set at 1.0 mL/minute, the temperature inlet and detector had been set at 300°C, and the oven temperature was programmed to initiate at 50°C and held for 1.5 minutes before being raised to 300°C at a rate 40°C/minute and held for 3 minutes. Sample pre-treatment by modification of the QuEChERS method includes using a relatively large amount of inorganic salt, extraction volume and extraction cycle. The optimal conditions for processing a 400 uL urine sample were 160 mg magnesium sulphate, 40 mg sodium chloride, and 400 uL acetonitrile for organic solvent. According to the validation test, the detection limit for methamphetamine was 0.36 ug/mL; the quantitation limit was 1.09 ug/mL, and the calibration curve followed the regression line. y=1.0489x-3.7914, coefficient (r) was 0.9973. The recovery of the analyte spiked into urine at 5, 7 and 9 ug/mL on average was 100.5±2.33% for intraday dan 93.3±7.21% for interday. The precision was excellent, with an average coefficient of variation of 2.31%. The procedure was applied to four urine samples from drug users and the first abuser (25.51 ug/mL), the second abuser (15.05 ug/mL), the third abuser (17.72 ug/mL) and the last abuser (3.08 ug/mL) were all satisfactorily quantitated.","PeriodicalId":21644,"journal":{"name":"Science and Technology Indonesia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49312086","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}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：