首页 > 最新文献

Bulletin of Chemical Reaction Engineering & Catalysis最新文献

英文 中文
Exploring Alkali Hydroxide Influence on Calcium Titanate Formation for Application in Biodiesel Catalysts 探索碱氢氧化物对生物柴油催化剂中应用的钛酸钙形成的影响
Pub Date : 2024-07-19 DOI: 10.9767/bcrec.20165
R. Puntharod, Kittikarnkorn Onsomsuay, P. Pookmanee, Jaturon Kumchompoo
Biodiesel has been recognized as the most widely utilized biofuel around the world due to its significant role in reducing the consumption of crude oil and lowering environmental pollution levels. By serving as a renewable alternative to fossil fuels, bioethanol helps decrease greenhouse gas emissions and contributes to a more sustainable energy future. Traditionally, alkali hydroxides like NaOH and KOH have been mainstays in biodiesel synthesis. However, their overuse can lead to unwanted byproducts and operational complexities. Since calcium titanate can occur at a strong base condition, it presents an alternative avenue worth exploring. In this study, we investigate the influence of alkali hydroxides, namely LiOH, NaOH, and KOH, on the formation of calcium titanate through hydrothermal methods, with varying heating times. We aim to understand how different hydroxides affect the synthesis process and the resultant properties of calcium titanate. We delve into the vibrational properties of Ca‒O‒Ti and Ti‒O bonds using Fourier transform infrared spectroscopy (FTIR), confirming the presence of calcium titanate (JCPDS No.42-0423) through X-ray diffractometry (XRD). This thorough characterization provides insight into the structural integrity and composition of the synthesized materials. Moreover, scanning electron microscopy (SEM) reveals the intriguing cube-like morphology of calcium titanate, offering visual evidence of its unique structure. The fatty acid methyl ester Iimpressively, our results show that calcium titanate synthesized in 7 M NaOH and KOH solutions, heated for 24 hours, emerges as a promising biodiesel catalyst. We observe fatty acid methyl ester provides the percentages of 63.67% and 90.02%, respectively, indicating the catalytic efficacy of these materials in biodiesel production. These findings not only contribute to the understanding of calcium titanate synthesis but also pave the way for a sustainable future in biodiesel production by introducing efficient and eco-friendly catalysts.
生物柴油在减少原油消耗和降低环境污染水平方面发挥着重要作用,因此被公认为全球使用最广泛的生物燃料。作为化石燃料的可再生替代品,生物乙醇有助于减少温室气体排放,为实现更可持续的能源未来做出贡献。传统上,NaOH 和 KOH 等碱氢氧化物是合成生物柴油的主要原料。然而,过度使用它们会导致不必要的副产品和操作复杂性。由于钛酸钙可在强碱条件下生成,它提供了一种值得探索的替代途径。在本研究中,我们研究了碱氢氧化物(即 LiOH、NaOH 和 KOH)对通过不同加热时间的水热法形成钛酸钙的影响。我们的目的是了解不同的氢氧化物如何影响钛酸钙的合成过程和最终特性。我们利用傅立叶变换红外光谱(FTIR)深入研究了 Ca-O-Ti 和 Ti-O 键的振动特性,并通过 X 射线衍射仪(XRD)确认了钛酸钙(JCPDS 编号:42-0423)的存在。这种全面的表征有助于深入了解合成材料的结构完整性和组成。此外,扫描电子显微镜(SEM)显示了钛酸钙有趣的立方体状形态,为其独特的结构提供了直观的证据。令人印象深刻的是,我们的研究结果表明,在 7 M NaOH 和 KOH 溶液中合成的钛酸钙在加热 24 小时后可成为一种很有前景的生物柴油催化剂。我们观察到脂肪酸甲酯的提供率分别为 63.67% 和 90.02%,这表明这些材料在生物柴油生产中具有催化功效。这些发现不仅有助于人们了解钛酸钙的合成,而且通过引入高效、环保的催化剂,为生物柴油生产的可持续发展铺平了道路。
{"title":"Exploring Alkali Hydroxide Influence on Calcium Titanate Formation for Application in Biodiesel Catalysts","authors":"R. Puntharod, Kittikarnkorn Onsomsuay, P. Pookmanee, Jaturon Kumchompoo","doi":"10.9767/bcrec.20165","DOIUrl":"https://doi.org/10.9767/bcrec.20165","url":null,"abstract":"Biodiesel has been recognized as the most widely utilized biofuel around the world due to its significant role in reducing the consumption of crude oil and lowering environmental pollution levels. By serving as a renewable alternative to fossil fuels, bioethanol helps decrease greenhouse gas emissions and contributes to a more sustainable energy future. Traditionally, alkali hydroxides like NaOH and KOH have been mainstays in biodiesel synthesis. However, their overuse can lead to unwanted byproducts and operational complexities. Since calcium titanate can occur at a strong base condition, it presents an alternative avenue worth exploring. In this study, we investigate the influence of alkali hydroxides, namely LiOH, NaOH, and KOH, on the formation of calcium titanate through hydrothermal methods, with varying heating times. We aim to understand how different hydroxides affect the synthesis process and the resultant properties of calcium titanate. We delve into the vibrational properties of Ca‒O‒Ti and Ti‒O bonds using Fourier transform infrared spectroscopy (FTIR), confirming the presence of calcium titanate (JCPDS No.42-0423) through X-ray diffractometry (XRD). This thorough characterization provides insight into the structural integrity and composition of the synthesized materials. Moreover, scanning electron microscopy (SEM) reveals the intriguing cube-like morphology of calcium titanate, offering visual evidence of its unique structure. The fatty acid methyl ester Iimpressively, our results show that calcium titanate synthesized in 7 M NaOH and KOH solutions, heated for 24 hours, emerges as a promising biodiesel catalyst. We observe fatty acid methyl ester provides the percentages of 63.67% and 90.02%, respectively, indicating the catalytic efficacy of these materials in biodiesel production. These findings not only contribute to the understanding of calcium titanate synthesis but also pave the way for a sustainable future in biodiesel production by introducing efficient and eco-friendly catalysts.","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":" 485","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141823761","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}
引用次数: 0
Performance of Hydrothermally Prepared NiMo Dispersed on Sulfated Zirconia Nano-Catalyst in The Conversion of Used Palm Cooking Oil into Jet Fuel Range Bio-Hydrocarbons 水热法制备的硫酸化氧化锆纳米催化剂上分散的镍钼在将废棕榈烹调油转化为喷气燃料系列生物烃中的表现
Pub Date : 2024-07-08 DOI: 10.9767/bcrec.20157
Karna Wijaya, Aldino Javier Saviola, Amalia Kurnia Amin, Marini Fairuz Vebryana, Adyatma Bhagaskara, Hilda Anggita Ekawati, Saffana Ramadhani, Dita Adi Saputra, A. Agustanhakri
Human efforts to overcome environmental problems from using fossil fuels continue, such as hydroconversion of biomass into bio-jet fuel. Research on producing a jet fuel range of bio-hydrocarbons from used palm cooking oil catalyzed by sulfated zirconia impregnated with nickel-molybdenum bimetal has been successfully conducted. The hydrothermal method synthesized the nano-catalyst material in the sulfation and impregnation processes. The hydroconversion process was carried out at atmospheric pressure and a temperature of 300–600 °C for 2 h with a hydrogen gas flow rate of 20 mL/min and a catalyst-to-feed ratio of 1:100 (wt%). Compared with zirconia and sulfated zirconia, NiMo-impregnated sulfated zirconia showed the best activity and selectivity in bio-jet fuel production with liquid product and selectivity of 61.07% and 43.49%, respectively. This catalyst also performed well in three consecutive runs, with bio-jet fuel selectivity in the second and third runs of 51.68% and 30.86%, respectively. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
人类一直在努力克服使用化石燃料带来的环境问题,例如将生物质加氢转化为生物喷气燃料。利用硫化氧化锆浸渍镍钼双金属催化废棕榈食用油生产生物烃类喷气燃料的研究已经取得成功。在硫酸盐化和浸渍过程中,水热法合成了纳米催化剂材料。氢气流速为 20 mL/min,催化剂与原料的比例为 1:100(重量比),在常压和 300-600 °C 的温度下进行了 2 小时的水热转化过程。与氧化锆和硫酸化氧化锆相比,镍钼浸渍硫酸化氧化锆在生物喷气燃料生产中表现出最好的活性和选择性,液体产物和选择性分别为 61.07% 和 43.49%。这种催化剂在连续三次运行中也表现出色,第二次和第三次运行中的生物喷气燃料选择性分别为 51.68% 和 30.86%。作者版权所有 © 2024 年,BCREC 出版集团出版。本文采用 CC BY-SA 许可协议 (https://creativecommons.org/licenses/by-sa/4.0) 公开发表。
{"title":"Performance of Hydrothermally Prepared NiMo Dispersed on Sulfated Zirconia Nano-Catalyst in The Conversion of Used Palm Cooking Oil into Jet Fuel Range Bio-Hydrocarbons","authors":"Karna Wijaya, Aldino Javier Saviola, Amalia Kurnia Amin, Marini Fairuz Vebryana, Adyatma Bhagaskara, Hilda Anggita Ekawati, Saffana Ramadhani, Dita Adi Saputra, A. Agustanhakri","doi":"10.9767/bcrec.20157","DOIUrl":"https://doi.org/10.9767/bcrec.20157","url":null,"abstract":"Human efforts to overcome environmental problems from using fossil fuels continue, such as hydroconversion of biomass into bio-jet fuel. Research on producing a jet fuel range of bio-hydrocarbons from used palm cooking oil catalyzed by sulfated zirconia impregnated with nickel-molybdenum bimetal has been successfully conducted. The hydrothermal method synthesized the nano-catalyst material in the sulfation and impregnation processes. The hydroconversion process was carried out at atmospheric pressure and a temperature of 300–600 °C for 2 h with a hydrogen gas flow rate of 20 mL/min and a catalyst-to-feed ratio of 1:100 (wt%). Compared with zirconia and sulfated zirconia, NiMo-impregnated sulfated zirconia showed the best activity and selectivity in bio-jet fuel production with liquid product and selectivity of 61.07% and 43.49%, respectively. This catalyst also performed well in three consecutive runs, with bio-jet fuel selectivity in the second and third runs of 51.68% and 30.86%, respectively. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":"117 5","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141666966","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}
引用次数: 0
The Effect of Solvent on the Characteristics of FeBTC MOF as a Potential Heterogenous Catalyst Prepared via Green Mechanochemical Process 溶剂对通过绿色机械化学工艺制备的潜在异源催化剂 FeBTC MOF 特性的影响
Pub Date : 2024-02-08 DOI: 10.9767/bcrec.20115
Indri Yati, Muhammad Ridwan, Franco Padella, M. Pentimalli
In this study, the synthesis of FeBTC (BTC = 1,3,5-benzenetricarboxylate) also known as MIL-100 (Fe) metal organic framework (MOF) has been carried out successfully using green mechanochemical method (neat grinding and liquid assisted grinding). The effect of solvent used in the synthesis was investigated for the first time to elucidate the physicochemical properties of FeBTC including crystal structure, thermal stability, pore size and specific surface area. The physicochemical properties of all FeBTC obtained in this study were compared to commercial FeBTC (Basolite F-300), characterized using powder X-Ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and nitrogen physisorption isotherms. All Fe-BTC MOF synthesized in this study showed improved textural properties compared to commercial Basolite F-300 such as higher crystallinity, higher surface area and larger pore size. It was found that the best synthesis method was by using the mixture of ethanol and water with equal volume ratio as solvent. The highest BET surface area of FeBTC synthesized using this method was 972 m2/g for FeBTC-EtOH/H2O. This value is 2.3 times higher than the surface area of commercial Basolite F-300 (418 m2/g). FeBTC with higher surface area is expected to have higher catalytic activity which makes this FeBTC an excellent candidate as a heterogenous catalyst for many reactions such as aldol condensation or esterification reaction. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
本研究采用绿色机械化学方法(纯研磨和液体辅助研磨)成功合成了 FeBTC(BTC = 1,3,5-苯三羧酸酯),也称为 MIL-100 (Fe)金属有机框架(MOF)。为了阐明 FeBTC 的理化性质,包括晶体结构、热稳定性、孔径和比表面积,首次研究了合成过程中所用溶剂的影响。本研究中获得的所有 FeBTC 的理化性质都与商用 FeBTC(Basolite F-300)进行了比较,并使用粉末 X 射线衍射(XRD)、热重分析(TGA)和氮物理吸附等温线进行了表征。与商用 Basolite F-300 相比,本研究合成的所有铁-BTC MOF 都具有更好的质构特性,如更高的结晶度、更高的比表面积和更大的孔径。研究发现,最佳的合成方法是使用等体积比的乙醇和水的混合物作为溶剂。用这种方法合成的 FeBTC 的最高 BET 表面积为 972 m2/g(FeBTC-EtOH/H2O)。该值是商用 Basolite F-300 表面积(418 m2/g)的 2.3 倍。具有较高表面积的铁基四氯化碳有望具有更高的催化活性,这使得这种铁基四氯化碳成为许多反应(如醛醇缩合或酯化反应)中异质催化剂的极佳候选材料。作者版权所有 © 2024 年,由 BCREC 出版集团出版。本文采用 CC BY-SA 许可协议 (https://creativecommons.org/licenses/by-sa/4.0) 公开发表。
{"title":"The Effect of Solvent on the Characteristics of FeBTC MOF as a Potential Heterogenous Catalyst Prepared via Green Mechanochemical Process","authors":"Indri Yati, Muhammad Ridwan, Franco Padella, M. Pentimalli","doi":"10.9767/bcrec.20115","DOIUrl":"https://doi.org/10.9767/bcrec.20115","url":null,"abstract":"In this study, the synthesis of FeBTC (BTC = 1,3,5-benzenetricarboxylate) also known as MIL-100 (Fe) metal organic framework (MOF) has been carried out successfully using green mechanochemical method (neat grinding and liquid assisted grinding). The effect of solvent used in the synthesis was investigated for the first time to elucidate the physicochemical properties of FeBTC including crystal structure, thermal stability, pore size and specific surface area. The physicochemical properties of all FeBTC obtained in this study were compared to commercial FeBTC (Basolite F-300), characterized using powder X-Ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and nitrogen physisorption isotherms. All Fe-BTC MOF synthesized in this study showed improved textural properties compared to commercial Basolite F-300 such as higher crystallinity, higher surface area and larger pore size. It was found that the best synthesis method was by using the mixture of ethanol and water with equal volume ratio as solvent. The highest BET surface area of FeBTC synthesized using this method was 972 m2/g for FeBTC-EtOH/H2O. This value is 2.3 times higher than the surface area of commercial Basolite F-300 (418 m2/g). FeBTC with higher surface area is expected to have higher catalytic activity which makes this FeBTC an excellent candidate as a heterogenous catalyst for many reactions such as aldol condensation or esterification reaction. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":"80 2","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139851037","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}
引用次数: 0
The Effect of Solvent on the Characteristics of FeBTC MOF as a Potential Heterogenous Catalyst Prepared via Green Mechanochemical Process 溶剂对通过绿色机械化学工艺制备的潜在异源催化剂 FeBTC MOF 特性的影响
Pub Date : 2024-02-08 DOI: 10.9767/bcrec.20115
Indri Yati, Muhammad Ridwan, Franco Padella, M. Pentimalli
In this study, the synthesis of FeBTC (BTC = 1,3,5-benzenetricarboxylate) also known as MIL-100 (Fe) metal organic framework (MOF) has been carried out successfully using green mechanochemical method (neat grinding and liquid assisted grinding). The effect of solvent used in the synthesis was investigated for the first time to elucidate the physicochemical properties of FeBTC including crystal structure, thermal stability, pore size and specific surface area. The physicochemical properties of all FeBTC obtained in this study were compared to commercial FeBTC (Basolite F-300), characterized using powder X-Ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and nitrogen physisorption isotherms. All Fe-BTC MOF synthesized in this study showed improved textural properties compared to commercial Basolite F-300 such as higher crystallinity, higher surface area and larger pore size. It was found that the best synthesis method was by using the mixture of ethanol and water with equal volume ratio as solvent. The highest BET surface area of FeBTC synthesized using this method was 972 m2/g for FeBTC-EtOH/H2O. This value is 2.3 times higher than the surface area of commercial Basolite F-300 (418 m2/g). FeBTC with higher surface area is expected to have higher catalytic activity which makes this FeBTC an excellent candidate as a heterogenous catalyst for many reactions such as aldol condensation or esterification reaction. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
本研究采用绿色机械化学方法(纯研磨和液体辅助研磨)成功合成了 FeBTC(BTC = 1,3,5-苯三羧酸酯),也称为 MIL-100 (Fe)金属有机框架(MOF)。为了阐明 FeBTC 的理化性质,包括晶体结构、热稳定性、孔径和比表面积,首次研究了合成过程中所用溶剂的影响。本研究中获得的所有 FeBTC 的理化性质都与商用 FeBTC(Basolite F-300)进行了比较,并使用粉末 X 射线衍射(XRD)、热重分析(TGA)和氮物理吸附等温线进行了表征。与商用 Basolite F-300 相比,本研究合成的所有铁-BTC MOF 都具有更好的质构特性,如更高的结晶度、更高的比表面积和更大的孔径。研究发现,最佳的合成方法是使用等体积比的乙醇和水的混合物作为溶剂。用这种方法合成的 FeBTC 的最高 BET 表面积为 972 m2/g(FeBTC-EtOH/H2O)。该值是商用 Basolite F-300 表面积(418 m2/g)的 2.3 倍。具有较高表面积的铁基四氯化碳有望具有更高的催化活性,这使得这种铁基四氯化碳成为许多反应(如醛醇缩合或酯化反应)中异质催化剂的极佳候选材料。作者版权所有 © 2024 年,由 BCREC 出版集团出版。本文采用 CC BY-SA 许可协议 (https://creativecommons.org/licenses/by-sa/4.0) 公开发表。
{"title":"The Effect of Solvent on the Characteristics of FeBTC MOF as a Potential Heterogenous Catalyst Prepared via Green Mechanochemical Process","authors":"Indri Yati, Muhammad Ridwan, Franco Padella, M. Pentimalli","doi":"10.9767/bcrec.20115","DOIUrl":"https://doi.org/10.9767/bcrec.20115","url":null,"abstract":"In this study, the synthesis of FeBTC (BTC = 1,3,5-benzenetricarboxylate) also known as MIL-100 (Fe) metal organic framework (MOF) has been carried out successfully using green mechanochemical method (neat grinding and liquid assisted grinding). The effect of solvent used in the synthesis was investigated for the first time to elucidate the physicochemical properties of FeBTC including crystal structure, thermal stability, pore size and specific surface area. The physicochemical properties of all FeBTC obtained in this study were compared to commercial FeBTC (Basolite F-300), characterized using powder X-Ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and nitrogen physisorption isotherms. All Fe-BTC MOF synthesized in this study showed improved textural properties compared to commercial Basolite F-300 such as higher crystallinity, higher surface area and larger pore size. It was found that the best synthesis method was by using the mixture of ethanol and water with equal volume ratio as solvent. The highest BET surface area of FeBTC synthesized using this method was 972 m2/g for FeBTC-EtOH/H2O. This value is 2.3 times higher than the surface area of commercial Basolite F-300 (418 m2/g). FeBTC with higher surface area is expected to have higher catalytic activity which makes this FeBTC an excellent candidate as a heterogenous catalyst for many reactions such as aldol condensation or esterification reaction. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":" 42","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139791179","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}
引用次数: 0
Optimization of Cu2O Thickness to Enhance Photocatalytic Properties of Electrodeposited Cu2O/FTO Photoanode 优化 Cu2O 厚度以增强电沉积 Cu2O/FTO 光阳极的光催化性能
Pub Date : 2024-02-07 DOI: 10.9767/bcrec.20081
Riza Ariyani Nur Khasanah, F. Chien, Rita Prasetyowati, R. Yudianti
Currently, n-type cuprous oxide (Cu2O) is a promising material as photocatalyst because of its energy gap of 2 eV that absorbs visible light up to a wavelength of 600 nm. As a photoelectrode, the thickness of Cu2O is crucial, where the improper thickness may worsen the photocatalytic properties. This work aimed to enhance the photocatalytic properties of Cu2O electrodeposited on fluorine-doped tin oxide (FTO), called Cu2O/FTO, by optimizing the Cu2O thickness. The thickness of Cu2O was controlled by adjusting the deposition time in the electrochemical deposition of Cu2O/FTO. By changing the deposition time from 5 to 45 min, the morphology of Cu2O changed from a leaf-like shape to an irregular facet shape with highly dense coverage, and the average thickness increased from 370 to 1100 nm. The increasing Cu2O thickness resulted in the increasing light absorption. The Cu2O/FTO demonstrated anodic photocurrent, which increased with the Cu2O thickness up to a threshold value of 1000 nm (35 min deposition time). At a thickness of 1000 nm, Cu2O/FTO achieved the highest photocurrent (150 and 58 µA under irradiation of 365 and 470 nm, respectively) due to the highly dense morphology and high absorption. In addition, with a thickness of 1000 nm, the charge diffusion was still good. Further, the increase of Cu2O film thickness higher than 1000 nm caused low photocatalytic properties even though the morphology was highly dense, and the absorption was the highest. This condition could be due to the relatively too-high resistance of Cu2O that caused poor charge diffusion. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
目前,n 型氧化亚铜(Cu2O)是一种很有前途的光催化剂材料,因为它的能隙为 2 eV,可吸收波长为 600 nm 的可见光。作为光电极,Cu2O 的厚度至关重要,厚度不当可能会降低光催化性能。本研究旨在通过优化 Cu2O 的厚度,提高电沉积在掺氟氧化锡(FTO)上的 Cu2O(Cu2O/FTO)的光催化性能。在 Cu2O/FTO 的电化学沉积过程中,通过调整沉积时间来控制 Cu2O 的厚度。将沉积时间从 5 分钟改为 45 分钟后,Cu2O 的形态从叶片状变为不规则的面状,覆盖层高度致密,平均厚度从 370 纳米增加到 1100 纳米。Cu2O 厚度的增加导致光吸收增加。Cu2O/FTO 显示出阳极光电流,随着 Cu2O 厚度的增加,阳极光电流增加到 1000 nm 的临界值(沉积时间为 35 分钟)。在厚度为 1000 纳米时,Cu2O/FTO 的光电流最高(在 365 纳米和 470 纳米的照射下分别为 150 微安和 58 微安),这归功于其高度致密的形貌和高吸收率。此外,在厚度为 1000 纳米时,电荷扩散仍然良好。此外,当 Cu2O 薄膜厚度增加到 1000 nm 以上时,尽管形貌高度致密且吸收率最高,但光催化性能却很低。这种情况可能是由于 Cu2O 的电阻过大,导致电荷扩散不畅。作者版权所有 © 2024 年,BCREC 出版集团出版。本文采用 CC BY-SA 许可协议 (https://creativecommons.org/licenses/by-sa/4.0) 公开发表。
{"title":"Optimization of Cu2O Thickness to Enhance Photocatalytic Properties of Electrodeposited Cu2O/FTO Photoanode","authors":"Riza Ariyani Nur Khasanah, F. Chien, Rita Prasetyowati, R. Yudianti","doi":"10.9767/bcrec.20081","DOIUrl":"https://doi.org/10.9767/bcrec.20081","url":null,"abstract":"Currently, n-type cuprous oxide (Cu2O) is a promising material as photocatalyst because of its energy gap of 2 eV that absorbs visible light up to a wavelength of 600 nm. As a photoelectrode, the thickness of Cu2O is crucial, where the improper thickness may worsen the photocatalytic properties. This work aimed to enhance the photocatalytic properties of Cu2O electrodeposited on fluorine-doped tin oxide (FTO), called Cu2O/FTO, by optimizing the Cu2O thickness. The thickness of Cu2O was controlled by adjusting the deposition time in the electrochemical deposition of Cu2O/FTO. By changing the deposition time from 5 to 45 min, the morphology of Cu2O changed from a leaf-like shape to an irregular facet shape with highly dense coverage, and the average thickness increased from 370 to 1100 nm. The increasing Cu2O thickness resulted in the increasing light absorption. The Cu2O/FTO demonstrated anodic photocurrent, which increased with the Cu2O thickness up to a threshold value of 1000 nm (35 min deposition time). At a thickness of 1000 nm, Cu2O/FTO achieved the highest photocurrent (150 and 58 µA under irradiation of 365 and 470 nm, respectively) due to the highly dense morphology and high absorption. In addition, with a thickness of 1000 nm, the charge diffusion was still good. Further, the increase of Cu2O film thickness higher than 1000 nm caused low photocatalytic properties even though the morphology was highly dense, and the absorption was the highest. This condition could be due to the relatively too-high resistance of Cu2O that caused poor charge diffusion. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":"142 2-3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139857616","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}
引用次数: 0
Optimization of Cu2O Thickness to Enhance Photocatalytic Properties of Electrodeposited Cu2O/FTO Photoanode 优化 Cu2O 厚度以增强电沉积 Cu2O/FTO 光阳极的光催化性能
Pub Date : 2024-02-07 DOI: 10.9767/bcrec.20081
Riza Ariyani Nur Khasanah, F. Chien, Rita Prasetyowati, R. Yudianti
Currently, n-type cuprous oxide (Cu2O) is a promising material as photocatalyst because of its energy gap of 2 eV that absorbs visible light up to a wavelength of 600 nm. As a photoelectrode, the thickness of Cu2O is crucial, where the improper thickness may worsen the photocatalytic properties. This work aimed to enhance the photocatalytic properties of Cu2O electrodeposited on fluorine-doped tin oxide (FTO), called Cu2O/FTO, by optimizing the Cu2O thickness. The thickness of Cu2O was controlled by adjusting the deposition time in the electrochemical deposition of Cu2O/FTO. By changing the deposition time from 5 to 45 min, the morphology of Cu2O changed from a leaf-like shape to an irregular facet shape with highly dense coverage, and the average thickness increased from 370 to 1100 nm. The increasing Cu2O thickness resulted in the increasing light absorption. The Cu2O/FTO demonstrated anodic photocurrent, which increased with the Cu2O thickness up to a threshold value of 1000 nm (35 min deposition time). At a thickness of 1000 nm, Cu2O/FTO achieved the highest photocurrent (150 and 58 µA under irradiation of 365 and 470 nm, respectively) due to the highly dense morphology and high absorption. In addition, with a thickness of 1000 nm, the charge diffusion was still good. Further, the increase of Cu2O film thickness higher than 1000 nm caused low photocatalytic properties even though the morphology was highly dense, and the absorption was the highest. This condition could be due to the relatively too-high resistance of Cu2O that caused poor charge diffusion. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
目前,n 型氧化亚铜(Cu2O)是一种很有前途的光催化剂材料,因为它具有 2 eV 的能隙,可以吸收波长为 600 nm 的可见光。作为光电极,Cu2O 的厚度至关重要,厚度不当可能会降低光催化性能。本研究旨在通过优化 Cu2O 的厚度,提高电沉积在掺氟氧化锡(FTO)(即 Cu2O/FTO)上的 Cu2O 的光催化性能。在 Cu2O/FTO 的电化学沉积过程中,通过调整沉积时间来控制 Cu2O 的厚度。将沉积时间从 5 分钟改为 45 分钟后,Cu2O 的形态从叶片状变为高密度覆盖的不规则面状,平均厚度从 370 纳米增加到 1100 纳米。Cu2O 厚度的增加导致光吸收增加。Cu2O/FTO 显示出阳极光电流,随着 Cu2O 厚度的增加,阳极光电流增加到 1000 nm 的临界值(沉积时间为 35 分钟)。在厚度为 1000 纳米时,Cu2O/FTO 的光电流最高(在 365 纳米和 470 纳米的照射下分别为 150 微安和 58 微安),这归功于其高度致密的形貌和高吸收率。此外,在厚度为 1000 纳米时,电荷扩散仍然良好。此外,当 Cu2O 薄膜厚度增加到 1000 nm 以上时,尽管形貌高度致密且吸收率最高,但光催化性能却很低。这种情况可能是由于 Cu2O 的电阻过大,导致电荷扩散不畅。作者版权所有 © 2024 年,BCREC 出版集团出版。本文采用 CC BY-SA 许可协议 (https://creativecommons.org/licenses/by-sa/4.0) 公开发表。
{"title":"Optimization of Cu2O Thickness to Enhance Photocatalytic Properties of Electrodeposited Cu2O/FTO Photoanode","authors":"Riza Ariyani Nur Khasanah, F. Chien, Rita Prasetyowati, R. Yudianti","doi":"10.9767/bcrec.20081","DOIUrl":"https://doi.org/10.9767/bcrec.20081","url":null,"abstract":"Currently, n-type cuprous oxide (Cu2O) is a promising material as photocatalyst because of its energy gap of 2 eV that absorbs visible light up to a wavelength of 600 nm. As a photoelectrode, the thickness of Cu2O is crucial, where the improper thickness may worsen the photocatalytic properties. This work aimed to enhance the photocatalytic properties of Cu2O electrodeposited on fluorine-doped tin oxide (FTO), called Cu2O/FTO, by optimizing the Cu2O thickness. The thickness of Cu2O was controlled by adjusting the deposition time in the electrochemical deposition of Cu2O/FTO. By changing the deposition time from 5 to 45 min, the morphology of Cu2O changed from a leaf-like shape to an irregular facet shape with highly dense coverage, and the average thickness increased from 370 to 1100 nm. The increasing Cu2O thickness resulted in the increasing light absorption. The Cu2O/FTO demonstrated anodic photocurrent, which increased with the Cu2O thickness up to a threshold value of 1000 nm (35 min deposition time). At a thickness of 1000 nm, Cu2O/FTO achieved the highest photocurrent (150 and 58 µA under irradiation of 365 and 470 nm, respectively) due to the highly dense morphology and high absorption. In addition, with a thickness of 1000 nm, the charge diffusion was still good. Further, the increase of Cu2O film thickness higher than 1000 nm caused low photocatalytic properties even though the morphology was highly dense, and the absorption was the highest. This condition could be due to the relatively too-high resistance of Cu2O that caused poor charge diffusion. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":"56 33","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139797950","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}
引用次数: 0
Lampung Natural Zeolite Dopped with of ZnO-TiO2 Metal Oxide as Catalyst for Biodiesel Production 掺杂氧化锌-二氧化钛金属氧化物的楠榜天然沸石作为催化剂用于生物柴油生产
Pub Date : 2024-01-09 DOI: 10.9767/bcrec.20038
M. Al Muttaqii, Maja Pranata Marbun, Sugeng Priyanto, Andreas Sibuea, W. Simanjuntak, Fuad Syafaat AM, Havier Samuel Huttur Silalahi Raja, R. Alviany, Tri Maryani, Triastuti Sulistyaningsih, Erik Prasetyo, S. Sudibyo, Indri Yati
Research has been carried out on making biodiesel from palm oil using natural zeolite catalysts impregnated with metal oxides such as zinc oxide and titanium oxide. This research aims to produce biodiesel using natural zeolite and ZnO-TiO2/NZ catalysts. The catalysts were analyzed using X-Ray Diffraction (XRD), X-Ray Fluorescence (XRF), Scanning Electron Microscope (SEM), and Brunauer-Emmet-Teller (BET). The catalyst was tested in the transesterification reaction to produce biodiesel. The mole oil and methanol ratio varied from 1:15, 1:18, and 1:20. In addition, the biodiesel product was analyzed using Gas Chromatography-Mass Spectroscopy (GC-MS). The results showed the optimum condition for converting triglycerides to 1:18 variation of oil:methanol was 60.53%using a ZnO-TiO2/NZ catalyst. The ZnO-TiO2/NZ catalyst is very promising for use as a catalyst for converting palm oils into biodiesel.
已有研究利用浸渍了氧化锌和氧化钛等金属氧化物的天然沸石催化剂从棕榈油中提取生物柴油。本研究旨在使用天然沸石和 ZnO-TiO2/NZ 催化剂生产生物柴油。使用 X 射线衍射 (XRD)、X 射线荧光 (XRF)、扫描电子显微镜 (SEM) 和布鲁诺-艾美特-泰勒 (BET) 对催化剂进行了分析。催化剂在生产生物柴油的酯交换反应中进行了测试。油和甲醇的摩尔比分别为 1:15、1:18 和 1:20。此外,还使用气相色谱-质谱法(GC-MS)对生物柴油产品进行了分析。结果表明,使用 ZnO-TiO2/NZ 催化剂将甘油三酯转化为 1:18 变化的油:甲醇的最佳条件为 60.53%。ZnO-TiO2/NZ 催化剂非常适合用作将棕榈油转化为生物柴油的催化剂。
{"title":"Lampung Natural Zeolite Dopped with of ZnO-TiO2 Metal Oxide as Catalyst for Biodiesel Production","authors":"M. Al Muttaqii, Maja Pranata Marbun, Sugeng Priyanto, Andreas Sibuea, W. Simanjuntak, Fuad Syafaat AM, Havier Samuel Huttur Silalahi Raja, R. Alviany, Tri Maryani, Triastuti Sulistyaningsih, Erik Prasetyo, S. Sudibyo, Indri Yati","doi":"10.9767/bcrec.20038","DOIUrl":"https://doi.org/10.9767/bcrec.20038","url":null,"abstract":"Research has been carried out on making biodiesel from palm oil using natural zeolite catalysts impregnated with metal oxides such as zinc oxide and titanium oxide. This research aims to produce biodiesel using natural zeolite and ZnO-TiO2/NZ catalysts. The catalysts were analyzed using X-Ray Diffraction (XRD), X-Ray Fluorescence (XRF), Scanning Electron Microscope (SEM), and Brunauer-Emmet-Teller (BET). The catalyst was tested in the transesterification reaction to produce biodiesel. The mole oil and methanol ratio varied from 1:15, 1:18, and 1:20. In addition, the biodiesel product was analyzed using Gas Chromatography-Mass Spectroscopy (GC-MS). The results showed the optimum condition for converting triglycerides to 1:18 variation of oil:methanol was 60.53%using a ZnO-TiO2/NZ catalyst. The ZnO-TiO2/NZ catalyst is very promising for use as a catalyst for converting palm oils into biodiesel.","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":" 15","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139628571","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}
引用次数: 0
The Properties and Activity of TiO2-based Nanorods as an Anti-Fouling Agent and a Photocatalyst 基于 TiO2 的纳米棒作为防污剂和光催化剂的特性和活性
Pub Date : 2024-01-02 DOI: 10.9767/bcrec.20074
Sri Wahyuni, Iindriana Kartini, Sri Kadarwati
The properties and activity of TiO2-based nanorods as an antifouling agent and a photocatalyst for the catalytic degradation of methylene blue (MB) have been investigated. A modification of TiO2 with SiO2 was first carried out to enlarge the surface area. In order to enhance the TiO­2 photo response to the visible light region, a further modification of TiO2-SiO2 (TS) composites with polyaniline (PANI) was also conducted. The nanorod TiO2 exhibited an anatase structure based on the diffraction patterns. The TEM images showed that some TiO2 molecules were attached around SiO2 with a random orientation. The TiO2-SiO2-PANI (TS-PANI) exhibited the largest specific surface area (SBET) of about 256.85 m2/g. The profile on the AFM images of the composites showed that the nano-roughness of the coatings was confirmed. The photocatalytic activity was evaluated through the decomposition of MB both on the powder and the coated composites. The photocatalytic activity on the coatings was verified due to further application as anti-fouling coatings involving photocatalytic mechanism. The decomposition of MB using TS-PANI powder and TS-PANI coating composites was 89.5% and 90.2 %, respectively, with the irradiation time on the coatings was 20 min longer. The anti-fouling activity through the photocatalytic mechanism and nano-roughness surface was confirmed by the inhibition of barnacle growth on the teakwood surface immersed for two months in the sea.
研究了基于二氧化钛的纳米棒作为防污剂和催化降解亚甲基蓝(MB)的光催化剂的特性和活性。首先用二氧化硅对二氧化钛进行改性,以增大其表面积。为了增强二氧化钛对可见光区域的光响应,还用聚苯胺(PANI)对二氧化钛-二氧化硅(TS)复合材料进行了进一步改性。根据衍射图样,纳米棒 TiO2 呈现锐钛矿结构。TEM 图像显示,一些 TiO2 分子以随机取向的方式附着在 SiO2 周围。TiO2-SiO2-PANI(TS-PANI)的比表面积(SBET)最大,约为 256.85 m2/g。复合材料的原子力显微镜图像轮廓显示,涂层的纳米通透性得到了证实。通过分解粉末和涂层复合材料上的甲基溴,对光催化活性进行了评估。涂层的光催化活性得到了验证,可进一步用作涉及光催化机制的防污涂层。使用 TS-PANI 粉末和 TS-PANI 涂层复合材料的甲基溴分解率分别为 89.5% 和 90.2%,涂层的照射时间延长了 20 分钟。在海水中浸泡两个月后,柚木表面的藤壶生长受到了抑制,这证实了光催化机理和纳米表面的防污活性。
{"title":"The Properties and Activity of TiO2-based Nanorods as an Anti-Fouling Agent and a Photocatalyst","authors":"Sri Wahyuni, Iindriana Kartini, Sri Kadarwati","doi":"10.9767/bcrec.20074","DOIUrl":"https://doi.org/10.9767/bcrec.20074","url":null,"abstract":"The properties and activity of TiO2-based nanorods as an antifouling agent and a photocatalyst for the catalytic degradation of methylene blue (MB) have been investigated. A modification of TiO2 with SiO2 was first carried out to enlarge the surface area. In order to enhance the TiO­2 photo response to the visible light region, a further modification of TiO2-SiO2 (TS) composites with polyaniline (PANI) was also conducted. The nanorod TiO2 exhibited an anatase structure based on the diffraction patterns. The TEM images showed that some TiO2 molecules were attached around SiO2 with a random orientation. The TiO2-SiO2-PANI (TS-PANI) exhibited the largest specific surface area (SBET) of about 256.85 m2/g. The profile on the AFM images of the composites showed that the nano-roughness of the coatings was confirmed. The photocatalytic activity was evaluated through the decomposition of MB both on the powder and the coated composites. The photocatalytic activity on the coatings was verified due to further application as anti-fouling coatings involving photocatalytic mechanism. The decomposition of MB using TS-PANI powder and TS-PANI coating composites was 89.5% and 90.2 %, respectively, with the irradiation time on the coatings was 20 min longer. The anti-fouling activity through the photocatalytic mechanism and nano-roughness surface was confirmed by the inhibition of barnacle growth on the teakwood surface immersed for two months in the sea.","PeriodicalId":505246,"journal":{"name":"Bulletin of Chemical Reaction Engineering & Catalysis","volume":"29 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139536868","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}
引用次数: 0
期刊
Bulletin of Chemical Reaction Engineering & Catalysis
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1