Pub Date : 2024-09-21DOI: 10.1007/s10934-024-01680-y
Shuai Zhang, Ning Yu, Yunyang Li, Pengyuan Zhang, Qichao Huang, Li Shen
{"title":"Correction: One-step synthesis of CuO/MCM-41 nanocomposites and their application in photocatalytic degradation of dyes","authors":"Shuai Zhang, Ning Yu, Yunyang Li, Pengyuan Zhang, Qichao Huang, Li Shen","doi":"10.1007/s10934-024-01680-y","DOIUrl":"10.1007/s10934-024-01680-y","url":null,"abstract":"","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 6","pages":"2191 - 2191"},"PeriodicalIF":2.5,"publicationDate":"2024-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142518487","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-09-04DOI: 10.1007/s10934-024-01679-5
Ching-Yu Wang, Kai Shen, John M. Vohs, Raymond J. Gorte
The effect of treating SBA-15 with a piranha solution at room temperature was studied for purposes of stabilizing a WO3 film deposited by Atomic Layer Deposition (ALD). For unmodified SBA-15, the film was found to migrate out of the SBA-15 pore structure between 573 and 773 K; however, WO3 remained within the pores in piranha-treated samples at 773 K, as demonstrated by X-Ray Diffraction and Transmission Electron Microscopy. Although N2 adsorption isotherms showed that the pore structure of SBA-15 was unaffected by the piranha treatment, the silanol content increased, as shown by water adsorption isotherms and Diffuse Reflectance Infrared Spectra of the silanol region. Temperature-programmed desorption results for 2-propanol also suggested that the silanols were more reactive in the piranha-treated samples. The results demonstrate the importance of surface modification of SBA-15 for the preparation of supported-oxide catalysts.
为了稳定通过原子层沉积 (ALD) 沉积的 WO3 薄膜,我们研究了在室温下用食人鱼溶液处理 SBA-15 的效果。通过 X 射线衍射和透射电子显微镜观察发现,对于未改性的 SBA-15,薄膜会在 573 至 773 K 之间从 SBA-15 孔隙结构中迁移出来;但是,在 773 K 时,经过食人鱼处理的样品中的 WO3 仍留在孔隙中。虽然 N2 吸附等温线表明 SBA-15 的孔隙结构不受食人鱼处理的影响,但硅醇含量却增加了,这一点可以从水吸附等温线和硅醇区域的漫反射红外光谱中看出。对 2-丙醇的温度编程解吸结果也表明,经过食人鱼处理的样品中硅烷醇的反应性更强。这些结果证明了 SBA-15 表面改性对制备支撑氧化物催化剂的重要性。
{"title":"Modification of SBA-15 for stabilizing supported oxides","authors":"Ching-Yu Wang, Kai Shen, John M. Vohs, Raymond J. Gorte","doi":"10.1007/s10934-024-01679-5","DOIUrl":"https://doi.org/10.1007/s10934-024-01679-5","url":null,"abstract":"<p>The effect of treating SBA-15 with a piranha solution at room temperature was studied for purposes of stabilizing a WO<sub>3</sub> film deposited by Atomic Layer Deposition (ALD). For unmodified SBA-15, the film was found to migrate out of the SBA-15 pore structure between 573 and 773 K; however, WO<sub>3</sub> remained within the pores in piranha-treated samples at 773 K, as demonstrated by X-Ray Diffraction and Transmission Electron Microscopy. Although N<sub>2</sub> adsorption isotherms showed that the pore structure of SBA-15 was unaffected by the piranha treatment, the silanol content increased, as shown by water adsorption isotherms and Diffuse Reflectance Infrared Spectra of the silanol region. Temperature-programmed desorption results for 2-propanol also suggested that the silanols were more reactive in the piranha-treated samples. The results demonstrate the importance of surface modification of SBA-15 for the preparation of supported-oxide catalysts.</p>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"262 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208683","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
High-performance carbon-based cathode materials were prepared by means of a facile eco-friendly and cost-effective molten salt carbonization of lotus leaves in eutectic (Na/K)2CO3 melt at 850 °C for aqueous zinc-ion hybrid supercapacitors (ZHSCs). Coin-type ZHSCs assembled as Carbon//Zn@Zn3(PO4)2 delivered 164.3 F g− 1 at 0.2 A g− 1 and 95.2 F g− 1 at 20 A g− 1 with capacitance retention of 57.9% using 2 M ZnSO4 solution as electrolyte. Meanwhile, it delivered the maximum energy density of 65.2 Wh kg− 1 at 169.0 W kg− 1 and the maximum power density of 13.3 kW kg− 1 at 23.3 Wh kg− 1. Benefitting from the multifunctionally interface-modified Zn3(PO4)2 layer acting as physical barrier and Zn2+-transfer ionic conductor, it revealed outstanding recyclability with capacitance retention of 96.6% and coulombic efficiency of 99.6% after 10,000 charge-discharge cycles at 1 A g-1. The synergistic effect on energy storage performance was discussed between porous structure, specific surface area, heteroatom doping and electrical conductivity.
通过对荷叶在共晶(Na/K)2CO3 熔体中进行 850 °C、环保且经济高效的熔盐碳化,制备了高性能碳基阴极材料,用于水性锌离子混合超级电容器(ZHSCs)。以 2 M ZnSO4 溶液为电解质,组装成 Carbon//Zn@Zn3(PO4)2 的硬币型 ZHSC 在 0.2 A g- 1 时的电容量为 164.3 F g- 1,在 20 A g- 1 时的电容量为 95.2 F g- 1,电容保持率为 57.9%。同时,在 169.0 W kg- 1 的条件下,它能提供 65.2 Wh kg- 1 的最大能量密度;在 23.3 Wh kg- 1 的条件下,它能提供 13.3 kW kg- 1 的最大功率密度。得益于作为物理屏障和 Zn2+ 转移离子导体的多功能界面修饰 Zn3(PO4)2 层,该电池具有出色的可回收性,在 1 A g-1 的条件下经过 10,000 次充放电循环后,电容保持率达到 96.6%,库仑效率达到 99.6%。讨论了多孔结构、比表面积、杂原子掺杂和导电性之间对储能性能的协同效应。
{"title":"Lotus leaf-derived capacitive carbon for zinc-ion hybrid supercapacitors prepared by one-step molten salt carbonization","authors":"Renze Pang, Jingwen Cui, Liwen Ding, Shaowei Wu, Xinhua Cheng","doi":"10.1007/s10934-024-01678-6","DOIUrl":"https://doi.org/10.1007/s10934-024-01678-6","url":null,"abstract":"<p>High-performance carbon-based cathode materials were prepared by means of a facile eco-friendly and cost-effective molten salt carbonization of lotus leaves in eutectic (Na/K)<sub>2</sub>CO<sub>3</sub> melt at 850 °C for aqueous zinc-ion hybrid supercapacitors (ZHSCs). Coin-type ZHSCs assembled as Carbon//Zn@Zn<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub> delivered 164.3 F g<sup>− 1</sup> at 0.2 A g<sup>− 1</sup> and 95.2 F g<sup>− 1</sup> at 20 A g<sup>− 1</sup> with capacitance retention of 57.9% using 2 M ZnSO<sub>4</sub> solution as electrolyte. Meanwhile, it delivered the maximum energy density of 65.2 Wh kg<sup>− 1</sup> at 169.0 W kg<sup>− 1</sup> and the maximum power density of 13.3 kW kg<sup>− 1</sup> at 23.3 Wh kg<sup>− 1</sup>. Benefitting from the multifunctionally interface-modified Zn<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub> layer acting as physical barrier and Zn<sup>2+</sup>-transfer ionic conductor, it revealed outstanding recyclability with capacitance retention of 96.6% and coulombic efficiency of 99.6% after 10,000 charge-discharge cycles at 1 A g<sup>-1</sup>. The synergistic effect on energy storage performance was discussed between porous structure, specific surface area, heteroatom doping and electrical conductivity.</p>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"103 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208684","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-27DOI: 10.1007/s10934-024-01677-7
Wenhui Wu, Kangrui Zhao, Kun Xiao
ZSM-5 is widely used in the field of catalysis due to its stability and tunability. Its acidity can be adjusted not only by varying the initial gel composition, but also by incorporating different types of template to enhance its performance. Both [Ga]-MFI and [Ga, Al]-MFI have demonstrated promising performance in the catalytic trioxane of formaldehyde synthesis. However, there is currently a paucity of research examining the influence of different templates on the catalytic performance of [Ga]-MFI and [Ga, Al]-MFI. The influence of different templates on the structure, morphology, and pore structure of the zeolite has been revealed through the application of characterisation techniques, including XRD, MAS NMR spectroscopy, ICP-OES, BET, and SEM. The impact of different templates on the acid properties of [Ga]-MFI and [Ga, Al]-MFI was assessed using NH3-TPD and Py-IR. The results of the experimental investigation into the catalytic performance of zeolites synthesised with larger molecular-structured templates indicate that these zeolites exhibit superior catalytic performance. Furthermore, the introduction of Na + ions has been observed to reduce the space-time yield of the products.
{"title":"Influence of various templates on the performance of MFI zeolite in catalytic synthesis of trioxane","authors":"Wenhui Wu, Kangrui Zhao, Kun Xiao","doi":"10.1007/s10934-024-01677-7","DOIUrl":"https://doi.org/10.1007/s10934-024-01677-7","url":null,"abstract":"<p>ZSM-5 is widely used in the field of catalysis due to its stability and tunability. Its acidity can be adjusted not only by varying the initial gel composition, but also by incorporating different types of template to enhance its performance. Both [Ga]-MFI and [Ga, Al]-MFI have demonstrated promising performance in the catalytic trioxane of formaldehyde synthesis. However, there is currently a paucity of research examining the influence of different templates on the catalytic performance of [Ga]-MFI and [Ga, Al]-MFI. The influence of different templates on the structure, morphology, and pore structure of the zeolite has been revealed through the application of characterisation techniques, including XRD, MAS NMR spectroscopy, ICP-OES, BET, and SEM. The impact of different templates on the acid properties of [Ga]-MFI and [Ga, Al]-MFI was assessed using NH<sub>3</sub>-TPD and Py-IR. The results of the experimental investigation into the catalytic performance of zeolites synthesised with larger molecular-structured templates indicate that these zeolites exhibit superior catalytic performance. Furthermore, the introduction of Na + ions has been observed to reduce the space-time yield of the products.</p>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"28 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208687","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-22DOI: 10.1007/s10934-024-01638-0
Lia Kouchachvili, Guillaume Gagnon-Caya, Reda Djebbar
High energy storage density, affordability, and environmental friendliness are the key requirements for materials used in thermal energy storage systems. A new composite thermal energy storage material (TESM) with all these requirements was fabricated by utilizing a biochar matrix. Biochar was derived from the slow pyrolysis of forestry residues, an abundant source of underutilized biomass in Canada. The results of this experimental study indicate that the carbonization conditions of the biomass affect the structure and surface morphology of the biochar and consequently its thermal properties. Amongst the carbonization conditions that were investigated in this study, a peak temperature of 800 °C with a heating rate of 2.5 °C/min yielded a biochar with an energy storage capacity of 508 J/g. This biochar was then used as a matrix for fabricating the composite TESM with salt hydrate. The composite showed high thermal stability after ten hydration/dehydration cycles with an average thermal energy storage capacity of 3795 J/g. The cost of thermal energy storage in this composite was found to be $0.50 CAD /kWhth.
{"title":"Wood-derived biochar as a matrix for cost-effective and high-performing composite thermal energy storage materials","authors":"Lia Kouchachvili, Guillaume Gagnon-Caya, Reda Djebbar","doi":"10.1007/s10934-024-01638-0","DOIUrl":"https://doi.org/10.1007/s10934-024-01638-0","url":null,"abstract":"<p>High energy storage density, affordability, and environmental friendliness are the key requirements for materials used in thermal energy storage systems. A new composite thermal energy storage material (TESM) with all these requirements was fabricated by utilizing a biochar matrix. Biochar was derived from the slow pyrolysis of forestry residues, an abundant source of underutilized biomass in Canada. The results of this experimental study indicate that the carbonization conditions of the biomass affect the structure and surface morphology of the biochar and consequently its thermal properties. Amongst the carbonization conditions that were investigated in this study, a peak temperature of 800 °C with a heating rate of 2.5 °C/min yielded a biochar with an energy storage capacity of 508 J/g. This biochar was then used as a matrix for fabricating the composite TESM with salt hydrate. The composite showed high thermal stability after ten hydration/dehydration cycles with an average thermal energy storage capacity of 3795 J/g. The cost of thermal energy storage in this composite was found to be $0.50 CAD /kWh<sub>th</sub>.</p>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"16 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-22DOI: 10.1007/s10934-024-01668-8
Xuzhi Shi, Yifeng Yu, Ruifa Yu, Ning Wang, Wei Lu, Xiaolin Han, Tangyao Sun, Pengcheng Li, Xiaodan Su, Zhaogang Teng, Ying Liu
Herein, copper sulfide loaded mesoporous organosilica nanospheres with a triple-shelled hollow structure (CuS/tHMONs) are successfully synthesized. The resulting CuS/tHMONs nanospheres exhibit a uniform diameter of 340 nm, mesoporous channels with a diameter of 3.8 nm, large pore volume, and triply separated cavities. High-angle annular dark-field scanning electron microscopy (HAADF-STEM) images confirm the presence of a high content of CuS nanoparticles within the CuS/tHMONs composite nanospheres. Moreover, the CuS/tHMONs nanospheres demonstrate high photothermal conversion efficiency and excellent photothermal stability. In vitro experiments reveal excellent biocompatibility of the CuS/tHMON nanospheres, and cytotoxic assays demonstrate their effectiveness in killing cancer cells through photothermal therapy.
{"title":"Facile synthesis of copper sulfide loaded mesoporous organosilica nanospheres with a triple-shelled hollow structure","authors":"Xuzhi Shi, Yifeng Yu, Ruifa Yu, Ning Wang, Wei Lu, Xiaolin Han, Tangyao Sun, Pengcheng Li, Xiaodan Su, Zhaogang Teng, Ying Liu","doi":"10.1007/s10934-024-01668-8","DOIUrl":"https://doi.org/10.1007/s10934-024-01668-8","url":null,"abstract":"<p>Herein, copper sulfide loaded mesoporous organosilica nanospheres with a triple-shelled hollow structure (CuS/tHMONs) are successfully synthesized. The resulting CuS/tHMONs nanospheres exhibit a uniform diameter of 340 nm, mesoporous channels with a diameter of 3.8 nm, large pore volume, and triply separated cavities. High-angle annular dark-field scanning electron microscopy (HAADF-STEM) images confirm the presence of a high content of CuS nanoparticles within the CuS/tHMONs composite nanospheres. Moreover, the CuS/tHMONs nanospheres demonstrate high photothermal conversion efficiency and excellent photothermal stability. In vitro experiments reveal excellent biocompatibility of the CuS/tHMON nanospheres, and cytotoxic assays demonstrate their effectiveness in killing cancer cells through photothermal therapy.</p>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"62 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-19DOI: 10.1007/s10934-024-01675-9
Jasmine M. Cox, Jessica J. Frick, Chen Liu, Zhou Li, Yaprak Ozbakir, Carlo Carraro, Roya Maboudian, Debbie G. Senesky
Graphene aerogel (GA) is a promising material for thermal management applications across many fields due to its lightweight and thermally insulative properties. However, standard values for important thermal properties, such as thermal conductivity, remain elusive due to the lack of reliable characterization techniques for highly porous materials. Comparative infrared thermal microscopy (CITM) is an attractive technique to obtain thermal conductance values of porous materials like GA, due to its non-invasive character, which requires no probing of, or contact with, the often delicate structures and frameworks. In this study, we improve upon CITM by utilizing a higher resolution imaging setup and reducing the need for pore-filling coating of the sample (previously used to adjust for emissivity). This upgraded setup, verified by characterizing porous silica aerogel, allows for a more accurate confirmation of the fundamental thermal conductivity value of GA while still accounting for the thermal resistance at material boundaries. Using this improved method, we measure a thermal conductivity below 0.036 W/m⋅K for commercial GA using multiple reference materials. These measurements demonstrate the impact of higher resolution thermal imaging to improve accuracy in low density, highly porous materials characterization. This study also reports thermal conductivity for much lower density (less than 15 mg/cm3) GA than previously published studies while maintaining the robustness of the CITM technique.
石墨烯气凝胶(GA)因其轻质和隔热性能,在许多领域的热管理应用中都是一种前景广阔的材料。然而,由于缺乏针对高多孔材料的可靠表征技术,热导率等重要热性能的标准值仍然难以确定。比较红外热显微镜(CITM)具有非侵入性的特点,无需探查或接触通常比较脆弱的结构和框架,因此是获取 GA 等多孔材料热导率值的一种有吸引力的技术。在本研究中,我们采用了分辨率更高的成像装置,并减少了对样品孔隙填充涂层(以前用于调整发射率)的需求,从而改进了 CITM。通过对多孔二氧化硅气凝胶的表征验证,这种升级后的设置可以更准确地确认 GA 的基本热导率值,同时还能考虑材料边界的热阻。利用这种改进的方法,我们使用多种参考材料测量出商用 GA 的热导率低于 0.036 W/m-K。这些测量结果证明了更高分辨率的热成像技术对提高低密度、高多孔材料表征精度的影响。与之前发表的研究相比,本研究还报告了密度更低(小于 15 毫克/立方厘米)的 GA 的热导率,同时保持了 CITM 技术的稳健性。
{"title":"Thermal conductivity of macroporous graphene aerogel measured using high resolution comparative infrared thermal microscopy","authors":"Jasmine M. Cox, Jessica J. Frick, Chen Liu, Zhou Li, Yaprak Ozbakir, Carlo Carraro, Roya Maboudian, Debbie G. Senesky","doi":"10.1007/s10934-024-01675-9","DOIUrl":"https://doi.org/10.1007/s10934-024-01675-9","url":null,"abstract":"<p>Graphene aerogel (GA) is a promising material for thermal management applications across many fields due to its lightweight and thermally insulative properties. However, standard values for important thermal properties, such as thermal conductivity, remain elusive due to the lack of reliable characterization techniques for highly porous materials. Comparative infrared thermal microscopy (CITM) is an attractive technique to obtain thermal conductance values of porous materials like GA, due to its non-invasive character, which requires no probing of, or contact with, the often delicate structures and frameworks. In this study, we improve upon CITM by utilizing a higher resolution imaging setup and reducing the need for pore-filling coating of the sample (previously used to adjust for emissivity). This upgraded setup, verified by characterizing porous silica aerogel, allows for a more accurate confirmation of the fundamental thermal conductivity value of GA while still accounting for the thermal resistance at material boundaries. Using this improved method, we measure a thermal conductivity below 0.036 W/m⋅K for commercial GA using multiple reference materials. These measurements demonstrate the impact of higher resolution thermal imaging to improve accuracy in low density, highly porous materials characterization. This study also reports thermal conductivity for much lower density (less than 15 mg/cm<sup>3</sup>) GA than previously published studies while maintaining the robustness of the CITM technique.</p>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"18 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208605","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-13DOI: 10.1007/s10934-024-01673-x
Cezar Augusto Moreira, Carlos Eduardo Scanferla, Angélica Gonçalves Oliveira, Vitor Anthony Duarte, Pedro Augusto Arroyo, Jéssica de Lara Andrade, Paulo Rodrigo Stival Bittencourt, Juliana Carla Garcia, Daniela Martins Fernandes de Oliveira
The search for efficient and more sustainable treatments of wastewater has become increasingly challenging in recent years. Aiming to contribute with this demand, the current study focused on the synthesis of mesoporous silica (MS) bio-adsorbents (MS1, MS2, MS3 and MS4) based on Santa Barbara Amorphous-15 (SBA-15) by a relatively simple and sustainable process using sodium silicate (SS) extracted from rice husk ashes (RHA) and Pluronic P123. Subtle and careful changes in the synthesis conditions resulted in MS samples with ordered pores and high specific surface area (SBET), that is, 712 m2 g−1 (MS1), 838 m2 g−1 (MS2), 905 m2 g−1 (MS3) and 806 m2 g−1 (MS4), which are higher than other silicas also produced from RHA, indicating that our bio-adsorbents may exhibit superior pollutant adsorption capabilities. In that regard, various research reports the potential of MS to adsorb dyes, heavy metals, bacteria, pharmaceuticals and other pollutants in model systems. However, our proposal advanced in testing the adsorbent potential of these materials for two independent systems: (i) removal of methylene blue (MB) model dye from aqueous solutions and (ii) treatment of an industrial denim laundry effluent. Indeed, all MS bio-adsorbents were potentially efficient and reusable, but MS1 and MS2 exhibited higher adsorption capacities for MB dye (qe = 327.29 and 365.78 mg g−1, respectively) at pH 12.0. The investigation of the effect of ions and DFT calculations contributed to elucidating the interactions between MB dye and MS bio-adsorbents. In addition, our bio-adsorbents stand out by their excellent efficiency (~ 75%) in the remediation of an industrial effluent exclusively by adsorption. Among the produced bio-adsorbents, MS2 has shown a higher degree of mesoscopic order, well-ordered and open-ended pores with oval architecture and interconnected hollow channels, but both MS1 and MS2 displayed similar adsorption capacities normalized by total surface area, demonstrating to be promising and eco-friendly adsorbents for use in environmental remediation.
{"title":"Bio-adsorbents based on mesoporous silica produced from rice husks with tunable architecture and surface area for remediation of industrial effluents","authors":"Cezar Augusto Moreira, Carlos Eduardo Scanferla, Angélica Gonçalves Oliveira, Vitor Anthony Duarte, Pedro Augusto Arroyo, Jéssica de Lara Andrade, Paulo Rodrigo Stival Bittencourt, Juliana Carla Garcia, Daniela Martins Fernandes de Oliveira","doi":"10.1007/s10934-024-01673-x","DOIUrl":"https://doi.org/10.1007/s10934-024-01673-x","url":null,"abstract":"<p>The search for efficient and more sustainable treatments of wastewater has become increasingly challenging in recent years. Aiming to contribute with this demand, the current study focused on the synthesis of mesoporous silica (MS) bio-adsorbents (MS1, MS2, MS3 and MS4) based on Santa Barbara Amorphous-15 (SBA-15) by a relatively simple and sustainable process using sodium silicate (SS) extracted from rice husk ashes (RHA) and Pluronic P123. Subtle and careful changes in the synthesis conditions resulted in MS samples with ordered pores and high specific surface area (<i>S</i><sub><i>BET</i></sub>), that is, 712 m<sup>2</sup> g<sup>−1</sup> (MS1), 838 m<sup>2</sup> g<sup>−1</sup> (MS2), 905 m<sup>2</sup> g<sup>−1</sup> (MS3) and 806 m<sup>2</sup> g<sup>−1</sup> (MS4), which are higher than other silicas also produced from RHA, indicating that our bio-adsorbents may exhibit superior pollutant adsorption capabilities. In that regard, various research reports the potential of MS to adsorb dyes, heavy metals, bacteria, pharmaceuticals and other pollutants in model systems. However, our proposal advanced in testing the adsorbent potential of these materials for two independent systems: (i) removal of methylene blue (MB) model dye from aqueous solutions and (ii) treatment of an industrial denim laundry effluent. Indeed, all MS bio-adsorbents were potentially efficient and reusable, but MS1 and MS2 exhibited higher adsorption capacities for MB dye (q<sub>e</sub> = 327.29 and 365.78 mg g<sup>−1</sup>, respectively) at pH 12.0. The investigation of the effect of ions and DFT calculations contributed to elucidating the interactions between MB dye and MS bio-adsorbents. In addition, our bio-adsorbents stand out by their excellent efficiency (~ 75%) in the remediation of an industrial effluent exclusively by adsorption. Among the produced bio-adsorbents, MS2 has shown a higher degree of mesoscopic order, well-ordered and open-ended pores with oval architecture and interconnected hollow channels, but both MS1 and MS2 displayed similar adsorption capacities normalized by total surface area, demonstrating to be promising and eco-friendly adsorbents for use in environmental remediation.</p>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"10 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142208686","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-12DOI: 10.1007/s10934-024-01670-0
Nga H. N. Do, Duyen My Thi Huynh, Trieu T. H. Le, Thanh V. N. Le, Hung D. Vuong, Trang P. T. Nguyen, Thao H. N. Quach, Phung K. Le, Anh C. Ha
Betel leaf extract (BLE) is well-known for its anti-bacterial, anti-inflammatory, and anti-oxidant activities as well as wound healing effects. For the first time, the ethanolic BLE has been successfully encapsulated into thermo-sensitive chitosan hydrogels to deliver the extract to infected wounds while preserving its biological activities. Morphologies, sol–gel transition, chemical structure, and pH of the hydrogels are comprehensively studied under the variation in the initial loading BLE concentration. Release kinetics of the hydrogels are evaluated in different environmental conditions to determine the BLE release behavior and the suitable mathematical model. The hydrogels exhibit sol–gel transition at 37.0–40.0 °C, a gelation time of 9.5–13.0 min at 37 °C, a neutral pH, and a hollow structure self-crosslinked by chitosan with both surface and internal adhesion of BLE. The BLE release from the hydrogels is affected by pH, temperature, and the BLE loading concentration and is governed by a controlled diffusion following the Korsmeyer-Peppas model. The hydrogels release 50.91–60.29% of their initial loading content and the release solutions demonstrate potent antibacterial activity against E. coli and S. aureus evidenced by the inhibition rate of 70.67–99.94%. Moreover, the chitosan hydrogels encapsulating BLE are biodegradable with a remarkably high degradability of 76.92–79.74% after 14 days of exposure to lysozyme under simulated physiological conditions. Based on the findings, the developed hydrogels are considered a potential delivery system to handle open skin wounds via local subcutaneous injection.
槟榔叶提取物(BLE)以其抗菌、消炎、抗氧化活性和伤口愈合效果而闻名。该研究首次成功地将乙醇槟榔叶提取物封装到热敏壳聚糖水凝胶中,以便在保持其生物活性的同时将提取物输送到受感染的伤口。在 BLE 初始负载浓度变化的情况下,对水凝胶的形态、溶胶-凝胶转变、化学结构和 pH 值进行了全面研究。评估了水凝胶在不同环境条件下的释放动力学,以确定 BLE 的释放行为和合适的数学模型。水凝胶在 37.0-40.0 °C时呈现溶胶-凝胶转变,37 °C时凝胶化时间为9.5-13.0分钟,pH值为中性,由壳聚糖自交联的中空结构同时具有BLE的表面和内部粘附性。BLE 从水凝胶中的释放受 pH 值、温度和 BLE 负载浓度的影响,并受 Korsmeyer-Peppas 模型的可控扩散控制。水凝胶的释放量为初始负载量的 50.91%-60.29%,释放溶液对大肠杆菌和金黄色葡萄球菌具有很强的抗菌活性,抑制率为 70.67%-99.94%。此外,包裹 BLE 的壳聚糖水凝胶是可生物降解的,在模拟生理条件下暴露于溶菌酶 14 天后,降解率高达 76.92-79.74%。根据研究结果,所开发的水凝胶被认为是一种潜在的输送系统,可通过局部皮下注射处理开放性皮肤伤口。
{"title":"Encapsulation of anti-bacterial Piper betle leaf extract in thermo-sensitive and biodegradable chitosan hydrogels: synthesis, characterization and release kinetics","authors":"Nga H. N. Do, Duyen My Thi Huynh, Trieu T. H. Le, Thanh V. N. Le, Hung D. Vuong, Trang P. T. Nguyen, Thao H. N. Quach, Phung K. Le, Anh C. Ha","doi":"10.1007/s10934-024-01670-0","DOIUrl":"10.1007/s10934-024-01670-0","url":null,"abstract":"<div><p>Betel leaf extract (BLE) is well-known for its anti-bacterial, anti-inflammatory, and anti-oxidant activities as well as wound healing effects. For the first time, the ethanolic BLE has been successfully encapsulated into thermo-sensitive chitosan hydrogels to deliver the extract to infected wounds while preserving its biological activities. Morphologies, sol–gel transition, chemical structure, and pH of the hydrogels are comprehensively studied under the variation in the initial loading BLE concentration. Release kinetics of the hydrogels are evaluated in different environmental conditions to determine the BLE release behavior and the suitable mathematical model. The hydrogels exhibit sol–gel transition at 37.0–40.0 °C, a gelation time of 9.5–13.0 min at 37 °C, a neutral pH, and a hollow structure self-crosslinked by chitosan with both surface and internal adhesion of BLE. The BLE release from the hydrogels is affected by pH, temperature, and the BLE loading concentration and is governed by a controlled diffusion following the Korsmeyer-Peppas model. The hydrogels release 50.91–60.29% of their initial loading content and the release solutions demonstrate potent antibacterial activity against <i>E. coli</i> and <i>S. aureus</i> evidenced by the inhibition rate of 70.67–99.94%. Moreover, the chitosan hydrogels encapsulating BLE are biodegradable with a remarkably high degradability of 76.92–79.74% after 14 days of exposure to lysozyme under simulated physiological conditions. Based on the findings, the developed hydrogels are considered a potential delivery system to handle open skin wounds via local subcutaneous injection.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 6","pages":"2291 - 2306"},"PeriodicalIF":2.5,"publicationDate":"2024-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141946751","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-08-09DOI: 10.1007/s10934-024-01676-8
Xiang Shi, Ke Wang, Minxin Wang, Hong Yuan
UiO-66 specimens having different acetic acid/ZrCl4 molar ratios were prepared and pyrolyzed to ZrO2 as supports for Pt and Ni, intended to catalyze the decarboxylation of oleic acid. Brunauer-Emmett-Teller surface area analyses, NH3 temperature-programmed desorption and pyridine adsorption infrared spectroscopy showed that the material made using an acetic acid/ZrCl4 molar ratio of 100 (ZrO2-100) had the largest specific surface area, acid amount and acid strength values. The yield of C8-C17 alkanes obtained from Ni/ZrO2-100 exceeded that provided by Pt/ZrO2-100 because the latter possessed more acidic sites than the former, which excessively cracked long-chain hydrocarbons. The 1 wt% Ni/ZrO2-100 catalyst showed the best catalytic performance, with 96.4% conversion of oleic acid and an 80.6% yield of C8-C17 alkanes after 4 h at 340 °C under a CO2 atmosphere at a pressure of 18 bar. The conversion of oleic acid remained almost unchanged after 4 reuses of this catalyst whereas the yield of C8-C17 alkanes decreased to 66.7%. This result is attributed to a loss of acidic sites and an increase in carbon build-up.
{"title":"Oleic acid decarboxylation to produce C8-C17 alkanes catalyzed by Pt and Ni on a MOF-derived zirconia","authors":"Xiang Shi, Ke Wang, Minxin Wang, Hong Yuan","doi":"10.1007/s10934-024-01676-8","DOIUrl":"10.1007/s10934-024-01676-8","url":null,"abstract":"<div><p>UiO-66 specimens having different acetic acid/ZrCl<sub>4</sub> molar ratios were prepared and pyrolyzed to ZrO<sub>2</sub> as supports for Pt and Ni, intended to catalyze the decarboxylation of oleic acid. Brunauer-Emmett-Teller surface area analyses, NH<sub>3</sub> temperature-programmed desorption and pyridine adsorption infrared spectroscopy showed that the material made using an acetic acid/ZrCl<sub>4</sub> molar ratio of 100 (ZrO<sub>2</sub>-100) had the largest specific surface area, acid amount and acid strength values. The yield of C<sub>8</sub>-C<sub>17</sub> alkanes obtained from Ni/ZrO<sub>2</sub>-100 exceeded that provided by Pt/ZrO<sub>2</sub>-100 because the latter possessed more acidic sites than the former, which excessively cracked long-chain hydrocarbons. The 1 wt% Ni/ZrO<sub>2</sub>-100 catalyst showed the best catalytic performance, with 96.4% conversion of oleic acid and an 80.6% yield of C<sub>8</sub>-C<sub>17</sub> alkanes after 4 h at 340 °C under a CO<sub>2</sub> atmosphere at a pressure of 18 bar. The conversion of oleic acid remained almost unchanged after 4 reuses of this catalyst whereas the yield of C<sub>8</sub>-C<sub>17</sub> alkanes decreased to 66.7%. This result is attributed to a loss of acidic sites and an increase in carbon build-up.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 6","pages":"2275 - 2289"},"PeriodicalIF":2.5,"publicationDate":"2024-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141924710","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}