Pub Date : 2025-01-01DOI: 10.1016/j.crgsc.2025.100482
Christopher Igwe Idumah
{"title":"Retraction notice to “Novel advancements in green and sustainable polymeric nanocomposites coatings” [Curr. Res. Green Sustain. Chem. 4 (2021) 100173]","authors":"Christopher Igwe Idumah","doi":"10.1016/j.crgsc.2025.100482","DOIUrl":"10.1016/j.crgsc.2025.100482","url":null,"abstract":"","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100482"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145044131","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 : 2025-01-01DOI: 10.1016/j.crgsc.2025.100484
Farzaneh Mohamadpour
An ecologically benign method for the synthesis of 1H-pyrazolo [1,2-b]phthalazine-5,10-dione scaffolds without the use of solvents is presented. It employs cerium (IV) sulfate tetrahydrate (Ce(SO4)2·4H2O) as a reusable heterogeneous Lewis acid catalyst. The reactions conclude significantly more quickly and produce products with impressive yields. This environmentally friendly technique employs safe settings. It is inexpensive, efficient, and simple to use. Finally, a solvent is not required. Furthermore, after four cycles, the highly efficient and eco-friendly Ce(SO4)2·4H2O remains rather stable and does not alter or lose its effectiveness. As a consequence, it is very advantageous for both cost-cutting and environmental protection during industrial operations. While the range of yields (79–92 %, with an average of 87.05 %) is fairly constant, the range of reaction times is fairly short (40–65 min, with an average of 48.52 min). It's also crucial that this method can provide yield excellent yields and a rapid rate of reaction even when used with a variety of functional groups that give or take electrons. The results suggest that, given relatively simple and effective reaction conditions, this technique is a productive one-pot procedure.
{"title":"Cerium (IV) sulfate tetrahydrate as a reusable heterogeneous Lewis acid catalyst: solvent-free and green synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione scaffolds","authors":"Farzaneh Mohamadpour","doi":"10.1016/j.crgsc.2025.100484","DOIUrl":"10.1016/j.crgsc.2025.100484","url":null,"abstract":"<div><div>An ecologically benign method for the synthesis of 1<em>H</em>-pyrazolo [1,2-<em>b</em>]phthalazine-5,10-dione scaffolds without the use of solvents is presented. It employs cerium (IV) sulfate tetrahydrate (Ce(SO<sub>4</sub>)<sub>2</sub>·4H<sub>2</sub>O) as a reusable heterogeneous Lewis acid catalyst. The reactions conclude significantly more quickly and produce products with impressive yields. This environmentally friendly technique employs safe settings. It is inexpensive, efficient, and simple to use. Finally, a solvent is not required. Furthermore, after four cycles, the highly efficient and eco-friendly Ce(SO<sub>4</sub>)<sub>2</sub>·4H<sub>2</sub>O remains rather stable and does not alter or lose its effectiveness. As a consequence, it is very advantageous for both cost-cutting and environmental protection during industrial operations. While the range of yields (79–92 %, with an average of 87.05 %) is fairly constant, the range of reaction times is fairly short (40–65 min, with an average of 48.52 min). It's also crucial that this method can provide yield excellent yields and a rapid rate of reaction even when used with a variety of functional groups that give or take electrons. The results suggest that, given relatively simple and effective reaction conditions, this technique is a productive one-pot procedure.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100484"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144925043","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 : 2025-01-01DOI: 10.1016/j.crgsc.2025.100496
Huaming Xie , Chuanjiang Pan , Ying Lei , Voranuch Thongpool , Weraporn Pivsa-Art , Sumonman Niamlang
Developing highly efficient metal-free electrocatalysts for oxygen reduction reaction (ORR) are pivotal for advancing sustainable fuel cell technology. An approach utilizing a green molten salt template to synthesize pyridinic-nitrogen (N)-enriched carbon aerogels (CA) with precisely engineered edge defects has been developed. CA was prepared by polymerizing chitosan gels embedded with potassium chloride/sodium chloride templates followed by controlled pyrolysis. Transmission electron microscopy, nitrogen adsorption–desorption analysis, X-ray photoelectron spectroscopy, and Raman characterization showed that the optimized catalyst, CA-3-900, possessed unique structural characteristics, including hierarchical porous structures with a high specific surface area (257 m2 g−1), high pyridinic-N content (32.48 %), and abundant edge defects. This is ascribed to the dual regulation of molten salt templates on porous structures and N configurations during carbonization. These structural merits resulted in exceptional ORR performance, including a high half-wave potential (0.78 V vs. reversible hydrogen electrode) and kinetic current density (2.81 mA cm−2 at 0.8 V). Notably, the improvement in ORR activity was mainly associated with the synergistic effect of edge-defective domains and rich pyridinic-N sites, as well as hierarchical porous channels favorable for catalytic site accessibility and mass/charge transport. Density functional theory (DFT) calculations revealed that pyridinic-N coupled with edge defects lowers the ORR overpotential, confirming the strong electronic coupling between pyridinic-N and adjacent defect sites effectively enhances O2 adsorption, intermediate conversion, and overall reaction kinetics. This study establishes a synthetic strategy for precisely manipulating N species and defects related to intrinsic activity in biomass-derived carbon catalysts, providing fundamental insights into defect-mediated catalytic enhancement mechanisms.
开发用于氧还原反应的高效无金属电催化剂是推进可持续燃料电池技术的关键。提出了一种利用绿色熔盐模板合成具有精确工程边缘缺陷的富吡啶氮(N)碳气凝胶的方法。以壳聚糖凝胶包埋氯化钾/氯化钠模板,经控制热解制备CA。透射电子显微镜、氮吸附-解吸分析、x射线光电子能谱和拉曼表征表明,优化后的催化剂CA-3-900具有独特的结构特征,具有高比表面积(257 m2 g−1)、高吡啶- n含量(32.48%)和丰富的边缘缺陷。这是由于炭化过程中熔盐模板对多孔结构和N构型的双重调节。这些结构优点导致了卓越的ORR性能,包括高半波电位(与可逆氢电极相比为0.78 V)和动态电流密度(0.8 V时为2.81 mA cm - 2)。值得注意的是,ORR活性的提高主要与边缘缺陷结构域和丰富的吡啶- n位点的协同作用以及有利于催化位点可达性和质量/电荷传输的分层多孔通道有关。密度泛函理论(DFT)计算表明,吡啶- n与边缘缺陷的耦合降低了ORR过电位,证实了吡啶- n与相邻缺陷位点之间的强电子耦合有效地增强了O2吸附、中间转化和整体反应动力学。本研究建立了一种精确操纵生物质衍生碳催化剂中N物种和与内在活性相关的缺陷的合成策略,为缺陷介导的催化增强机制提供了基础见解。
{"title":"Green molten salt template–Assisted synthesis of defect-rich carbon aerogels with abundant pyridinic-N sites for enhanced oxygen reduction electrocatalysis","authors":"Huaming Xie , Chuanjiang Pan , Ying Lei , Voranuch Thongpool , Weraporn Pivsa-Art , Sumonman Niamlang","doi":"10.1016/j.crgsc.2025.100496","DOIUrl":"10.1016/j.crgsc.2025.100496","url":null,"abstract":"<div><div>Developing highly efficient metal-free electrocatalysts for oxygen reduction reaction (ORR) are pivotal for advancing sustainable fuel cell technology. An approach utilizing a green molten salt template to synthesize pyridinic-nitrogen (N)-enriched carbon aerogels (CA) with precisely engineered edge defects has been developed. CA was prepared by polymerizing chitosan gels embedded with potassium chloride/sodium chloride templates followed by controlled pyrolysis. Transmission electron microscopy, nitrogen adsorption–desorption analysis, X-ray photoelectron spectroscopy, and Raman characterization showed that the optimized catalyst, CA-3-900, possessed unique structural characteristics, including hierarchical porous structures with a high specific surface area (257 m<sup>2</sup> g<sup>−1</sup>), high pyridinic-N content (32.48 %), and abundant edge defects. This is ascribed to the dual regulation of molten salt templates on porous structures and N configurations during carbonization. These structural merits resulted in exceptional ORR performance, including a high half-wave potential (0.78 V <em>vs</em>. reversible hydrogen electrode) and kinetic current density (2.81 mA cm<sup>−2</sup> at 0.8 V). Notably, the improvement in ORR activity was mainly associated with the synergistic effect of edge-defective domains and rich pyridinic-N sites, as well as hierarchical porous channels favorable for catalytic site accessibility and mass/charge transport. Density functional theory (DFT) calculations revealed that pyridinic-N coupled with edge defects lowers the ORR overpotential, confirming the strong electronic coupling between pyridinic-N and adjacent defect sites effectively enhances O<sub>2</sub> adsorption, intermediate conversion, and overall reaction kinetics. This study establishes a synthetic strategy for precisely manipulating N species and defects related to intrinsic activity in biomass-derived carbon catalysts, providing fundamental insights into defect-mediated catalytic enhancement mechanisms.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100496"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145525275","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 : 2025-01-01DOI: 10.1016/j.crgsc.2025.100498
S.G. Ganapathy Kumaresh, M. Ananthkumar
Corrosion significantly compromises the durability of reinforced concrete structures, leading to progressive strength loss and eventual structural failure. This study aims to develop an eco-friendly, organic carbon-based coating for mild steel using carbon derived from sugarcane bagasse and eggshell, with the objective of enhancing corrosion resistance. The findings suggest that a synergistic combination of amorphous and crystalline carbon phases improves the protective properties of the coating. Various coating formulations were prepared, including 100 % sugarcane bagasse (SG100 %), 100 % eggshell (ES100 %), and composite blends of 25 % eggshell + 75 % sugarcane bagasse (ES25 %+SG75 %), 50 % eggshell + 50 % sugarcane bagasse (ES50 %+SG50 %), and 75 % eggshell + 25 % sugarcane bagasse (ES75 %+SG25 %). Coated mild steel strips were immersed in 3.5 % NaCl contaminated simulated concrete pore solution (SCPS) to mimic a saline environment, and in 0.5 M HCl to represent an acidic medium. Corrosion behavior was evaluated through potentiodynamic polarization studies, supported by physicochemical characterization, mechanical testing, and COMSOL simulation. Among the tested formulations, the ES50 %+SG50 % composite exhibited superior corrosion resistance, with corrosion rates of 0.04 mm/year in SCPS and 1.06 mm/year in HCl. Furthermore, no visible morphological or structural degradation was observed after 2000 test cycles, confirming the coating's stability and effectiveness as a corrosion-resistant barrier for reinforced concrete applications.
{"title":"Dual-phase bio-carbon coatings for mild steel protection: A green approach using sugarcane bagasse and eggshell waste","authors":"S.G. Ganapathy Kumaresh, M. Ananthkumar","doi":"10.1016/j.crgsc.2025.100498","DOIUrl":"10.1016/j.crgsc.2025.100498","url":null,"abstract":"<div><div>Corrosion significantly compromises the durability of reinforced concrete structures, leading to progressive strength loss and eventual structural failure. This study aims to develop an eco-friendly, organic carbon-based coating for mild steel using carbon derived from sugarcane bagasse and eggshell, with the objective of enhancing corrosion resistance. The findings suggest that a synergistic combination of amorphous and crystalline carbon phases improves the protective properties of the coating. Various coating formulations were prepared, including 100 % sugarcane bagasse (SG100 %), 100 % eggshell (ES100 %), and composite blends of 25 % eggshell + 75 % sugarcane bagasse (ES25 %+SG75 %), 50 % eggshell + 50 % sugarcane bagasse (ES50 %+SG50 %), and 75 % eggshell + 25 % sugarcane bagasse (ES75 %+SG25 %). Coated mild steel strips were immersed in 3.5 % NaCl contaminated simulated concrete pore solution (SCPS) to mimic a saline environment, and in 0.5 M HCl to represent an acidic medium. Corrosion behavior was evaluated through potentiodynamic polarization studies, supported by physicochemical characterization, mechanical testing, and COMSOL simulation. Among the tested formulations, the ES50 %+SG50 % composite exhibited superior corrosion resistance, with corrosion rates of 0.04 mm/year in SCPS and 1.06 mm/year in HCl. Furthermore, no visible morphological or structural degradation was observed after 2000 test cycles, confirming the coating's stability and effectiveness as a corrosion-resistant barrier for reinforced concrete applications.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100498"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145575948","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 : 2025-01-01DOI: 10.1016/j.crgsc.2025.100495
Achmet Said Mohamed, Laurent Lemée
Microwave-assisted distillation (MAD) was compared with wood-heated distillation (WHD) and laboratory-scale distillation (LD) for the production of ylang-ylang essential oil. The yield of total essential oil collected by MAD was 29 % higher than WHD and 23 % higher than LD, while the distillation time was significantly reduced. Indeed, the oil was recovered within 40 min with 2.7 % yield using MAD, whereas LD and WHD required 19 h. The quality of the collected fractions was EXTRA SUP (ES), EXTRA (E), grade I, II and III according to density, ester index and refractive index. MAD produced 81 % high quality ES and E, 16 % grade I and 2 % low quality grade III fractions. WHD and LD produced approximately 15 % ES, 15 % grade I and 70 % grade III fractions. At the molecular level, 15 compounds were identified by GC-MS according to the French ISO standard. The higher amount of odoriferous light oxygenated compounds and lower amount of sesquiterpenic hydrocarbons in ES and Grade I fractions collected with MAD confirmed its high quality. Moreover, the Grade III fraction obtained with MAD showed a high content of oxygenated compounds compared to LD and WHD.
对微波辅助蒸馏法(MAD)与木材加热蒸馏法(WHD)和实验室蒸馏法(LD)生产依兰精油进行了比较。蒸馏法的总精油得率比蒸馏法高29%,比蒸馏法高23%,蒸馏法的时间显著缩短。事实上,使用MAD在40分钟内以2.7%的收率回收了油,而LD和WHD则需要19小时。根据密度,酯指数和折射率,收集的馏分的质量为EXTRA SUP (ES), EXTRA (E), I级,II级和III级。MAD生产了81%的优质ES和E, 16%的I级和2%的低质量III级馏分。WHD和LD分别产生约15%的ES、15%的I级和70%的III级馏分。在分子水平上,根据法国ISO标准,用GC-MS鉴定了15个化合物。用MAD提取的ES级馏分和I级馏分中有气味的轻氧化合物含量较高,倍半萜烯烃含量较低,证实了其高质量。此外,与LD和WHD相比,MAD获得的III级馏分显示出高含氧化合物含量。
{"title":"Microwave-assisted distillation of ylang-ylang flowers: A sustainable and efficient approach for essential oil extraction","authors":"Achmet Said Mohamed, Laurent Lemée","doi":"10.1016/j.crgsc.2025.100495","DOIUrl":"10.1016/j.crgsc.2025.100495","url":null,"abstract":"<div><div>Microwave-assisted distillation (MAD) was compared with wood-heated distillation (WHD) and laboratory-scale distillation (LD) for the production of ylang-ylang essential oil. The yield of total essential oil collected by MAD was 29 % higher than WHD and 23 % higher than LD, while the distillation time was significantly reduced. Indeed, the oil was recovered within 40 min with 2.7 % yield using MAD, whereas LD and WHD required 19 h. The quality of the collected fractions was EXTRA SUP (ES), EXTRA (E), grade I, II and III according to density, ester index and refractive index. MAD produced 81 % high quality ES and E, 16 % grade I and 2 % low quality grade III fractions. WHD and LD produced approximately 15 % ES, 15 % grade I and 70 % grade III fractions. At the molecular level, 15 compounds were identified by GC-MS according to the French ISO standard. The higher amount of odoriferous light oxygenated compounds and lower amount of sesquiterpenic hydrocarbons in ES and Grade I fractions collected with MAD confirmed its high quality. Moreover, the Grade III fraction obtained with MAD showed a high content of oxygenated compounds compared to LD and WHD.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100495"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145412428","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 : 2025-01-01DOI: 10.1016/j.crgsc.2025.100499
Mokhtar A. Babatabar, Ahmad Tavasoli
The growing demand for sustainable energy and the environmental challenges associated with fossil fuel dependence have intensified the search for efficient waste-to-fuel pathways. In this study, the co-pyrolysis of acid-washed pinewood biomass (APW) with used engine oil (UEO) is shown to exhibit a distinct synergistic interaction (a 1.66 % yield enhancement compared to the theoretical additive value), where non-linear hydrogen transfer from hydrocarbon-rich UEO fragments stabilizes oxygenated intermediates derived from APW. This unique effect not only enhances the overall liquid yield but also improves the hydrocarbon quality of the resulting bio-oil. Experiments were carried out in a fixed-bed reactor, and the operating parameters—temperature (400–600 °C), reaction time (20–60 min), carrier gas flow rate (5–25 mL/min), and UEO/feedstock ratio (10–50 wt%)—were optimized using response surface methodology (RSM). The highest bio-oil yield of 71.33 wt% was obtained at 520 °C, 25 min, 20 mL/min, and 50 wt% UEO. GC-MS and elemental analysis revealed substantial deoxygenation and hydrocarbon enrichment (70.23 wt%), yielding a fuel comparable to conventional diesel. These findings underscore the potential of APW–UEO co-pyrolysis as an innovative and sustainable approach to valorizing mixed waste streams into diesel-like biofuels.
{"title":"Co-pyrolysis of pinewood biomass and used engine oil waste: A sustainable approach to diesel-like biofuel production","authors":"Mokhtar A. Babatabar, Ahmad Tavasoli","doi":"10.1016/j.crgsc.2025.100499","DOIUrl":"10.1016/j.crgsc.2025.100499","url":null,"abstract":"<div><div>The growing demand for sustainable energy and the environmental challenges associated with fossil fuel dependence have intensified the search for efficient waste-to-fuel pathways. In this study, the co-pyrolysis of acid-washed pinewood biomass (APW) with used engine oil (UEO) is shown to exhibit a distinct synergistic interaction (a 1.66 % yield enhancement compared to the theoretical additive value), where non-linear hydrogen transfer from hydrocarbon-rich UEO fragments stabilizes oxygenated intermediates derived from APW. This unique effect not only enhances the overall liquid yield but also improves the hydrocarbon quality of the resulting bio-oil. Experiments were carried out in a fixed-bed reactor, and the operating parameters—temperature (400–600 °C), reaction time (20–60 min), carrier gas flow rate (5–25 mL/min), and UEO/feedstock ratio (10–50 wt%)—were optimized using response surface methodology (RSM). The highest bio-oil yield of 71.33 wt% was obtained at 520 °C, 25 min, 20 mL/min, and 50 wt% UEO. GC-MS and elemental analysis revealed substantial deoxygenation and hydrocarbon enrichment (70.23 wt%), yielding a fuel comparable to conventional diesel. These findings underscore the potential of APW–UEO co-pyrolysis as an innovative and sustainable approach to valorizing mixed waste streams into diesel-like biofuels.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100499"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145620666","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}
White pepper generally used as spice, has the main component of piperine which gives it a spicy taste and essential oils that determine its aroma. In general trade, only good pepper is traded, while off-grade that does not meet quality requirements will be wasted. This study aims to investigate the effect of extraction methods of essential oils from off-grade white pepper and the potential of its antimicrobial activity against pathogenic bacteria. The results showed that off-grade white pepper essential oils (WPEO) could be isolated by using microwave-assisted hydro-distillation (MAHD) and hydro-distillation (HD). Essential oils produced had physicochemical characteristics in accordance with the ISO 3061:2008 standard. Specifically, MAHD off-grade, MAHD grade-A, and HD WPEO had 13, 11, and 15 components, respectively. The chemical composition showed that all the extracted EO contained the main components of caryophyllene, (+)-3-carene, d-limonene, and β-pinene. The methods showed the extraction ability of monoterpene hydrocarbons by MAHD and sesquiterpene hydrocarbons by HD. In comparison, microwave-extracted essential oils had a higher limonene, while off-grade WPEO contained (+)-3-carene. The FTIR results confirmed the content of the components in the three WPEO that were investigated. All essential oils had antibacterial activity against E. coli and S. typhimurium with zone inhibition values of MAHD off-grade WPEO, MAHD grade-A WPEO, and HD off-grade WPEO against E. coli at 15.44 ± 1.68 mm, 6.72 ± 0.59 mm, and 10.17 ± 0.29 mm, as well as against S. typhimurium at 8.72 ± 1.25 mm, 8.06 ± 0.86 mm, and 8.83 ± 0.87 mm, respectively.
{"title":"Phytochemistry and antimicrobial potential of off-grade white pepper (Piper nigrum L.) essential oils extracted using microwave-assisted hydro-distillation (MAHD)","authors":"Sarifah Nurjanah , Sekar Widyaningrum , Bambang Nurhadi , S. Rosalinda , Rienoviar , Nandang Permadi , Euis Julaeha","doi":"10.1016/j.crgsc.2025.100450","DOIUrl":"10.1016/j.crgsc.2025.100450","url":null,"abstract":"<div><div>White pepper generally used as spice, has the main component of piperine which gives it a spicy taste and essential oils that determine its aroma. In general trade, only good pepper is traded, while off-grade that does not meet quality requirements will be wasted. This study aims to investigate the effect of extraction methods of essential oils from off-grade white pepper and the potential of its antimicrobial activity against pathogenic bacteria. The results showed that off-grade white pepper essential oils (WPEO) could be isolated by using microwave-assisted hydro-distillation (MAHD) and hydro-distillation (HD). Essential oils produced had physicochemical characteristics in accordance with the ISO 3061:2008 standard. Specifically, MAHD off-grade, MAHD grade-A, and HD WPEO had 13, 11, and 15 components, respectively. The chemical composition showed that all the extracted EO contained the main components of caryophyllene, (+)-3-carene, <span>d</span>-limonene, and β-pinene. The methods showed the extraction ability of monoterpene hydrocarbons by MAHD and sesquiterpene hydrocarbons by HD. In comparison, microwave-extracted essential oils had a higher limonene, while off-grade WPEO contained (+)-3-carene. The FTIR results confirmed the content of the components in the three WPEO that were investigated. All essential oils had antibacterial activity against E. coli and <em>S. typhimurium</em> with zone inhibition values of MAHD off-grade WPEO, MAHD grade-A WPEO, and HD off-grade WPEO against E. coli at 15.44 ± 1.68 mm, 6.72 ± 0.59 mm, and 10.17 ± 0.29 mm, as well as against <em>S. typhimurium</em> at 8.72 ± 1.25 mm, 8.06 ± 0.86 mm, and 8.83 ± 0.87 mm, respectively.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"10 ","pages":"Article 100450"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143548531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cocoa bean shells, a major byproduct of the cocoa industry, hold significant potential for value-added applications, particularly in cosmetics. The aim of this study was to develop a sustainable, eco-friendly extraction process for bioactive compounds with skin-whitening properties using microwave-assisted extraction (MAE) and polyol-based solvents, a novel approach in cocoa bean shell valorization. Polyols, such as propylene glycol (PG), were compared to ethanol (EtOH) for their efficiency in extracting bioactive compounds. The influence of polyol type, polyol concentration, solid-to-liquid ratio, temperature, and extraction time on total phenolic content (TPC), total flavonoid content (TFC), and tyrosinase inhibitory activity was systematically evaluated. This study demonstrated that PG, at optimal conditions (60 % w/v, 1:50 solid-to-liquid ratio, 100 °C, 30-min extraction), significantly enhanced TPC (59.57 ± 1.33 mg GAE/g sample), TFC (242.24 ± 2.95 mg QE/g sample), and tyrosinase inhibition (4.75 ± 0.35 mg KAE/g sample) compared to EtOH. LC-QQQ analysis identified quercetin, catechin, and trigonelline as key contributors to tyrosinase inhibition and melanin content reduction, with PG extracts demonstrating superior functional activity despite similar quercetin levels in both solvents. Comparative cytotoxicity, anti-melanogenic assays, and cellular tyrosinase inhibition further confirmed the enhanced safety and efficacy of PG extracts over conventional ethanol extracts, positioning them as a novel green solvent system for developing effective skin-whitening active ingredients in cosmetic formulations.
{"title":"Exploration of cosmetic bioactive compounds from cocoa bean shell using polyol-based microwave-assisted extraction: Cytotoxicity, anti-tyrosinase, and anti-melanogenesis properties","authors":"Sasakorn Pattanakitjaroenchai , Puthita Pitsawong , Nuntawat Khat-Udomkiri","doi":"10.1016/j.crgsc.2025.100454","DOIUrl":"10.1016/j.crgsc.2025.100454","url":null,"abstract":"<div><div>Cocoa bean shells, a major byproduct of the cocoa industry, hold significant potential for value-added applications, particularly in cosmetics. The aim of this study was to develop a sustainable, eco-friendly extraction process for bioactive compounds with skin-whitening properties using microwave-assisted extraction (MAE) and polyol-based solvents, a novel approach in cocoa bean shell valorization. Polyols, such as propylene glycol (PG), were compared to ethanol (EtOH) for their efficiency in extracting bioactive compounds. The influence of polyol type, polyol concentration, solid-to-liquid ratio, temperature, and extraction time on total phenolic content (TPC), total flavonoid content (TFC), and tyrosinase inhibitory activity was systematically evaluated. This study demonstrated that PG, at optimal conditions (60 % w/v, 1:50 solid-to-liquid ratio, 100 °C, 30-min extraction), significantly enhanced TPC (59.57 ± 1.33 mg GAE/g sample), TFC (242.24 ± 2.95 mg QE/g sample), and tyrosinase inhibition (4.75 ± 0.35 mg KAE/g sample) compared to EtOH. LC-QQQ analysis identified quercetin, catechin, and trigonelline as key contributors to tyrosinase inhibition and melanin content reduction, with PG extracts demonstrating superior functional activity despite similar quercetin levels in both solvents. Comparative cytotoxicity, anti-melanogenic assays, and cellular tyrosinase inhibition further confirmed the enhanced safety and efficacy of PG extracts over conventional ethanol extracts, positioning them as a novel green solvent system for developing effective skin-whitening active ingredients in cosmetic formulations.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"10 ","pages":"Article 100454"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143792574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-01DOI: 10.1016/j.crgsc.2025.100461
Ashraf Alsafasfeh
This study introduces Tetrabutyl Ammonium Chloride (TBAC) as a novel selective collector for silicates in the reverse flotation of apatite-quartz model sample. Zeta potential measurements, contact angle analysis, FTIR, and X-ray fluorescence spectroscopy (XPS) were employed to investigate reagent adsorption at mineral-water interfaces. FTIR analysis revealed the appearance of new peaks corresponding to C–H and C–N stretching in TBAC-treated quartz, but not in apatite, indicating TBAC's preferential adsorption on quartz surfaces. XPS analysis further supported FTIR results; a distinct N 1s peak at 401.5 eV was observed on TBAC-treated quartz, while no such peak appeared on apatite, confirming the absence of significant interaction. Zeta potential measurements showed a larger shift in surface charge for quartz than for apatite after TBAC treatment, particularly at higher pH levels, with a notable shift of +16.28 mV at pH 11 for quartz, compared to only +0.4 mV for apatite. Contact angle measurements also demonstrated that TBAC significantly increased quartz hydrophobicity—reaching values above 115°—while apatite showed minimal change. Flotation tests were conducted to evaluate the performance of TBAC as collector for apatite and quartz. In single mineral flotation, the highest quartz recovery (97 %) was achieved at pH 11 with a TBAC dosage of 150 g/ton while the apatite recovery was reduced to 31.6 %. The binary-mineral system showed a higher recovery of apatite with a commercial quartz collector at 52.4 %, compared to just 25.3 % when TBAC was used. Comparative tests with a conventional DA collector revealed that apatite recovery was significantly higher with DA (52.4 %) than with TBAC (25.3 %), emphasizing TBAC's limited interaction with phosphate minerals and its potential utility for silicate removal in reverse flotation processes.
{"title":"Selective flotation of silicates from phosphates using Tetrabutyl Ammonium Chloride as a green collector","authors":"Ashraf Alsafasfeh","doi":"10.1016/j.crgsc.2025.100461","DOIUrl":"10.1016/j.crgsc.2025.100461","url":null,"abstract":"<div><div>This study introduces Tetrabutyl Ammonium Chloride (TBAC) as a novel selective collector for silicates in the reverse flotation of apatite-quartz model sample. Zeta potential measurements, contact angle analysis, FTIR, and X-ray fluorescence spectroscopy (XPS) were employed to investigate reagent adsorption at mineral-water interfaces. FTIR analysis revealed the appearance of new peaks corresponding to C–H and C–N stretching in TBAC-treated quartz, but not in apatite, indicating TBAC's preferential adsorption on quartz surfaces. XPS analysis further supported FTIR results; a distinct N 1s peak at 401.5 eV was observed on TBAC-treated quartz, while no such peak appeared on apatite, confirming the absence of significant interaction. Zeta potential measurements showed a larger shift in surface charge for quartz than for apatite after TBAC treatment, particularly at higher pH levels, with a notable shift of +16.28 mV at pH 11 for quartz, compared to only +0.4 mV for apatite. Contact angle measurements also demonstrated that TBAC significantly increased quartz hydrophobicity—reaching values above 115°—while apatite showed minimal change. Flotation tests were conducted to evaluate the performance of TBAC as collector for apatite and quartz. In single mineral flotation, the highest quartz recovery (97 %) was achieved at pH 11 with a TBAC dosage of 150 g/ton while the apatite recovery was reduced to 31.6 %. The binary-mineral system showed a higher recovery of apatite with a commercial quartz collector at 52.4 %, compared to just 25.3 % when TBAC was used. Comparative tests with a conventional DA collector revealed that apatite recovery was significantly higher with DA (52.4 %) than with TBAC (25.3 %), emphasizing TBAC's limited interaction with phosphate minerals and its potential utility for silicate removal in reverse flotation processes.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"10 ","pages":"Article 100461"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144068559","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 : 2025-01-01DOI: 10.1016/j.crgsc.2025.100493
Uma Sakthivel PhD (Guest Teacher) , Sukumar P
Biological nutrient removal in SBRs requires the optimized sequencing of aerobic and anoxic phases to balance nitrification, denitrification and energy use. This study uses GPS-X v8.1 to simulate a 212 m3 SBR treating synthetic domestic wastewater (COD 2,500–3,500 mg L−1; TN ≈ 60 mg N L−1) under a 24-h cycle (1 h fill, 20 h react, 2 h settle/decant, 1 h idle) with DO setpoint of 2.0 mgL−1. Eleven operational strategies—including pre-anoxic, post-anoxic, intermittent aeration and their combinations—were evaluated. The model was calibrated and validated against independent plant data (R2 ≥ 0.85; NSE ≥0.70). A combined pre-anoxic + post-anoxic + intermittent aeration configuration delivered the best trade-off, achieving 87.1 % TN removal and 88.6 % TP removal while maintaining BOD and COD removal >89 % and a moderate energy penalty. Sensitivity and multi-objective optimization (TN removal vs energy) identified SRT, internal recirculation ratio and aerobic fraction as dominant controls and produced Pareto-optimal aeration schedules for practical implementation. These results provide actionable guidance for energy-efficient SBR operation to meet stringent nutrient targets.
{"title":"Optimizing reaction configurations of sequential batch reactor (SBR) for nitrogen removal from wastewater","authors":"Uma Sakthivel PhD (Guest Teacher) , Sukumar P","doi":"10.1016/j.crgsc.2025.100493","DOIUrl":"10.1016/j.crgsc.2025.100493","url":null,"abstract":"<div><div>Biological nutrient removal in SBRs requires the optimized sequencing of aerobic and anoxic phases to balance nitrification, denitrification and energy use. This study uses GPS-X v8.1 to simulate a 212 m<sup>3</sup> SBR treating synthetic domestic wastewater (COD 2,500–3,500 mg L<sup>−1</sup>; TN ≈ 60 mg N L<sup>−1</sup>) under a 24-h cycle (1 h fill, 20 h react, 2 h settle/decant, 1 h idle) with DO setpoint of 2.0 mgL<sup>−1</sup>. Eleven operational strategies—including pre-anoxic, post-anoxic, intermittent aeration and their combinations—were evaluated. The model was calibrated and validated against independent plant data (R<sup>2</sup> ≥ 0.85; NSE ≥0.70). A combined pre-anoxic + post-anoxic + intermittent aeration configuration delivered the best trade-off, achieving 87.1 % TN removal and 88.6 % TP removal while maintaining BOD and COD removal >89 % and a moderate energy penalty. Sensitivity and multi-objective optimization (TN removal vs energy) identified SRT, internal recirculation ratio and aerobic fraction as dominant controls and produced Pareto-optimal aeration schedules for practical implementation. These results provide actionable guidance for energy-efficient SBR operation to meet stringent nutrient targets.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100493"},"PeriodicalIF":0.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145462786","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}