Qingling Liao, Fumin Ma, Yongjun Fu, Wei Feng, Ying Lu
{"title":"Bi-functionalized MCM-41 for heavy metal ions removal: synthesis, enhanced performance and mechanism study","authors":"Qingling Liao, Fumin Ma, Yongjun Fu, Wei Feng, Ying Lu","doi":"10.1007/s10934-024-01642-4","DOIUrl":"10.1007/s10934-024-01642-4","url":null,"abstract":"<div><p>This work reports the amine and mercapto bi-functionalized mesoporous silica MCM-41 for heavy metal ions removal from aqueous solutions. XRD, FTIR and N<sub>2</sub> adsorption–desorption analyses confirmed that a series of bi-functionalized mesoporous silica MCM-41 with huge specific surface area were successfully obtained. In aqueous solution, the adsorption performance were evaluated by the adsorption of Zn(II), Cu(II), Cr(III) and Pb(II). The obtained results indicate that synthesis process has no significant influence on the structure and the existence of functional group resulted in outstanding adsorption capacity. The methodology of pre-hydrolysis was one effective treatment for grafting useful functional group on to mesoporous silica. The adsorption reactions for the adsorption of heavy metal ions by bi-functionalized silica-based mesoporous materials were spontaneous adsorption processes over the range of experimental temperatures. The adsorption isotherm is consistent with the Freundlich adsorption isotherms model. The Freundlich parameters K<sub>F</sub> and n indicated favorable adsorption. The adsorption kinetics of heavy metalions over these bi-functionalized mesoporous silica could be well described by pseudo-second-order models. Therefore, this bi-functionalized mesoporous material has promise for the removal and recovery of heavy metal ions from water.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1895 - 1904"},"PeriodicalIF":2.5,"publicationDate":"2024-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141380600","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}
{"title":"Vapour phase hydrodeoxygenation of Guaiacol using Ni/SBA-15 for bio-oil upgrading","authors":"Kayalvizhi Jeevanandham, Deepika Sekar, Pandurangan Arumugam","doi":"10.1007/s10934-024-01643-3","DOIUrl":"10.1007/s10934-024-01643-3","url":null,"abstract":"<div><p>The primary aim of this study is to break down the methoxy (-OCH<sub>3</sub>) and hydroxyl(-OH) oxygenates present in lignin, a component of biomass. This degradation was performed on a lignin-derived model compound, guaiacol, using a highly effective Ni-loaded SBA-15 catalyst. SBA-15 was synthesized via a hydrothermal method, and varying amounts of NiO (5, 10, 15, 20, 25 wt%) were incorporated into SBA-15 through wet impregnation. The catalysts were characterized by using techniques such as XRD, DRS-UV, FT-IR, TPR, BET, SEM, and HR-TEM. Their catalytic performance was evaluated through the hydrodeoxygenation of guaiacol in a vapor phase reactor under controlled atmospheric pressure conditions. Notably, at 200 °C with a hydrogen flow rate of 50 ml/h, the 10 wt% NiO/SBA-15 catalyst demonstrated superior catalytic activity, achieving high guaiacol conversion and aimed product selectivity.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1881 - 1893"},"PeriodicalIF":2.5,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141253131","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}
{"title":"Controllable synthesis of porous MxS@C composites (M = fe, Cu, Mn) with highly efficient electromagnetic absorption properties","authors":"Wenhui Zhang, Xinbo Wu, Dazhi Wang, Weijie Cai","doi":"10.1007/s10934-024-01601-z","DOIUrl":"10.1007/s10934-024-01601-z","url":null,"abstract":"<div><p>As the frequency range of electronic devices gradually expands, exploring frequency insensitive electromagnetic wave adsorption (EWA) materials that can achieve effective absorption in all bands has aroused great interest. A series of Fe<sub>1 − x</sub>S@C composite materials with three-dimensional conductive networks were successfully prepared in this work. In the preparation process, poly (aryl ether sulfone) with branched carboxylic (PAES-C) was selected as the skeleton and Fe<sup>3+</sup> ions were introduced via chemical adsorption. The main purpose of this work was to develop array porous composite materials with good EWA property. The work proposed a novel controllable method for preparing metal sulfides to explore the electromagnetic wave absorption. This routine was also developed to prepare other M<sub>x</sub>S@C composites (M = Fe, Cu, Mn). Compared to Mn<sub>x</sub>S@C and Cu<sub>x</sub>S@C composites, the RL<sub>min</sub> value of Fe<sub>1 − x</sub>S@C-4 was − 40.6 dB at 13.52 GHz, and at a thickness of 1.5 mm the effective bandwidth reached 3.12 GHz. Furthermore, its effective absorption band covered Ku, X, and C radar bands at different thicknesses.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1865 - 1879"},"PeriodicalIF":2.5,"publicationDate":"2024-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141253137","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}
{"title":"Enhanced Fischer-Tropsch synthesis performance on fe + ZSM5 bifunctional catalysts","authors":"Yulan Zhang, Xizhu Lin","doi":"10.1007/s10934-024-01641-5","DOIUrl":"10.1007/s10934-024-01641-5","url":null,"abstract":"<div><p>Fischer-Tropsch synthesis (FTS) is viewed as an effective method for producing clean fuels. Catalysts with high activity and selectivity, especially the latter, are the key to improving the catalytic performance. Herein, we report the preparation of an excellent bifunctional Fe + ZSM5 catalyst by employing novel hierarchical porous Fe<sub>2</sub>O<sub>3</sub> cage particles as FTS sites and porous ZSM5 as catalytic cracking sites. The selectivity for gasoline fuels (C<sub>5</sub>-C<sub>11</sub>) selectivity over the Fe + ZSM5(33) catalyst is as high as 65.1 wt%, which is greater than that of traditional outstanding than the traditionally zeolite-supported and physically mixed bifunctional catalysts. The enhanced catalytic performance can be attributed to the weak acid content governing the catalytic cracking. ZSM5 zeolite with a suitable weak acid content and desorption temperature can facilitate the cracking of C<sub>12+</sub> hydrocarbons, thereby facilitating the C<sub>5</sub>-C<sub>11</sub> selectivity and inhibiting the deactivation of active sites resulting from the aggregation of C<sub>12+</sub> hydrocarbons. Fe + ZSM5(27) with an suitable weak acid content provides a higher CO conversion of 93.6% combined with an excellent C<sub>5</sub>-C<sub>11</sub> selectivity of 62.7 wt%. This finding provides a promising strategy for designing bifunctional catalysts with controllable product distribution.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1853 - 1863"},"PeriodicalIF":2.5,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141194586","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}
Abdul Qayoom Mugheri, Muhammad Rafique Daudpoto, Arsalan Ahmed Mugheri, Dost Muhammad Kalhoro
{"title":"Retraction Note: Recent progress in doping-induced structural and electronic modification in Cu–SnCo interconnected network enhanced efficient performance evidence for the hydrogen evolution reaction: current state and prospects","authors":"Abdul Qayoom Mugheri, Muhammad Rafique Daudpoto, Arsalan Ahmed Mugheri, Dost Muhammad Kalhoro","doi":"10.1007/s10934-024-01645-1","DOIUrl":"10.1007/s10934-024-01645-1","url":null,"abstract":"","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 4","pages":"1543 - 1543"},"PeriodicalIF":2.5,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142409291","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}
Hsin Her Yu, Chia-Hua Lin, Jung-Ling Chang, Min-Yu Chen, Ci-Pei Lin, Hsu-Feng Lee
{"title":"Preparation of activated carbon composite electrode from sugarcane bagasse and its application on energy storage devices","authors":"Hsin Her Yu, Chia-Hua Lin, Jung-Ling Chang, Min-Yu Chen, Ci-Pei Lin, Hsu-Feng Lee","doi":"10.1007/s10934-024-01644-2","DOIUrl":"10.1007/s10934-024-01644-2","url":null,"abstract":"<div><p>Based on sustainable resource recycling, we utilize physical and chemical activation to modify sugarcane bagasse into activated carbon materials with a porous structure. The activated carbon modified with KOH-KNO<sub>3</sub> exhibits a high specific surface area and excellent specific capacitance, and the fabricated composite electrode demonstrates superior electrical conductivity of 57mS/cm. Subsequently, a supercapacitor containing an electrode, gel electrolyte, and separator is assembled in a sandwich structure. It achieves a specific capacitance of 262.4 F/g, an energy density of 17.9 Wh/kg, and a power density of 2021 W/kg at a scanning rate of 0.02 V/s. Furthermore, the supercapacitor demonstrates excellent cycle stability since it can maintain 98.38% of its initial capacitance after 20,000 cycles of charge and discharge under a constant current. In addition, the KOH-KNO<sub>3</sub>-modified activated carbon composite electrode exhibited superior electrochemical performance after we compared it to other carbon electrode supercapacitors derived from agricultural wastes.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1839 - 1852"},"PeriodicalIF":2.5,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141194769","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}
M. N. Mirzayev, G. T. Imanova, D. Neov, M. Rasoul, I. R. Bekpulatov, F. K. Khallokov, E. P. Popov, K. Hasanov, S. Isayeva, B. Mauyey, D. M. Mirzayeva, F. Tatardar, M. Dinu, G. Kaminski, A. Vladescu (Dragomir)
{"title":"Correction: Surface evaluation of carbonitride coating materials at high temperature: an investigation of oxygen adsorption on crystal surfaces by molecular dynamics simulation","authors":"M. N. Mirzayev, G. T. Imanova, D. Neov, M. Rasoul, I. R. Bekpulatov, F. K. Khallokov, E. P. Popov, K. Hasanov, S. Isayeva, B. Mauyey, D. M. Mirzayeva, F. Tatardar, M. Dinu, G. Kaminski, A. Vladescu (Dragomir)","doi":"10.1007/s10934-024-01637-1","DOIUrl":"10.1007/s10934-024-01637-1","url":null,"abstract":"","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 4","pages":"1541 - 1541"},"PeriodicalIF":2.5,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142414962","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}
{"title":"A facile approach to prepare Cu(I) based adsorbents for selective CO adsorption with excellent oxidation resistance ability","authors":"Faju Zhuang, Shougui Wang, Guanghui Chen, Fei Gao, Jingru Dou, Jipeng Dong","doi":"10.1007/s10934-024-01639-z","DOIUrl":"10.1007/s10934-024-01639-z","url":null,"abstract":"<div><p>Cu(I)-based adsorbents are currently the most commonly used CO adsorbents due to their high adsorption capacity and adsorption selectivity for CO. In order to achieve a facile preparation and improved antioxidant performance of Cu(I)-based adsorbents, in this work, a series of Cu(I) based CO adsorbents were designed and prepared by choosing CuCl<sub>2</sub> as the precursor, ultra-stable Y-type molecular sieves (USY) as the support, and methyl cellulose (MC) as a solid reductant. The MC introduction not only can reduce the precursor CuCl<sub>2</sub> to the active component CuCl, but also play a key role in improving the antioxidant performance of the adsorbent. The optimized adsorbent CuCl(5.0)@USY-MC(8%) exhibits an excellent antioxidant performance, maintaining 76% of CO adsorption capacity of fresh adsorbent after being placed in the air for 24 h. In addition, the adsorbent shows the high adsorption capacity, adsorption selectivity and good cycling stability for CO. The excellent CO adsorption performance as well as good antioxidant ability make the developed adsorbent a promising candidate for the efficient CO adsorption and separation from the gas mixture.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1827 - 1837"},"PeriodicalIF":2.5,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141194867","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}
Manjusha J. Gavhane, R. K. Jha, Kyung-Wan Nam, Deu S. Bhange
{"title":"Preparation and structural characterization of disordered Na-gallosilicate zeolite with natrolite framework and its K+ and NH4+ exchanged analogues","authors":"Manjusha J. Gavhane, R. K. Jha, Kyung-Wan Nam, Deu S. Bhange","doi":"10.1007/s10934-024-01631-7","DOIUrl":"10.1007/s10934-024-01631-7","url":null,"abstract":"<div><p>We report first time preparation and crystal structure of NH<sub>4</sub><sup>+</sup> exchanged form of highly disordered gallosilicate zeolite with natrolite framework (NAT) by ion exchange method from K-gallosilicate zeolite with natrolite framework. K<sup>+</sup> exchanged form was obtained by ion exchange with hydrothermally prepared highly disordered sodium gallosilicate zeolite with natrolite framework. Phase purity, degree of ion exchange, particle morphology, elemental mapping and thermal behaviour of Na-, K-, NH<sub>4</sub>-gallosilicate zeolites were investigated using various instrumental techniques. Crystal structures of Na-, K-, NH<sub>4</sub>-gallosilicate zeolites were obtained by Rietveld analysis of powder X-ray diffraction data collected using synchrotron source of X-rays. Refined structural models of hydrated Na-, K-, NH<sub>4</sub>-gallosilicate zeolites were compared. NH<sub>4</sub>-gallosilicate zeolite was calcined at 450 °C to obtain its H-form. The structure collapse of H-gallosilicate zeolite with natrolite framework is commented finally based on the structural characterization data.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1817 - 1825"},"PeriodicalIF":2.5,"publicationDate":"2024-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141166892","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}
{"title":"A novel high-efficiency In-based catalyst for ethylbenzene dehydrogenation with CO2","authors":"Quanhua Wang, Ruiqi Wei, Meng Pan, Yanchao Liu, Lichen Zhang, Jiajun Zheng, Shuwei Chen, Yuhao Zong, Hu Wang, Kaifei Yin, Yanwei Yue, Jinke Li","doi":"10.1007/s10934-024-01633-5","DOIUrl":"10.1007/s10934-024-01633-5","url":null,"abstract":"<div><p>A series of binary In<sub>2</sub>O<sub>3</sub>/S (S = Al<sub>2</sub>O<sub>3</sub>, SiO<sub>2</sub>, and MgO) catalysts were fabricated by an incipient-wetness impregnation method, which were firstly applied in the ethylbenzene dehydrogenation under the presence of CO<sub>2</sub> (EBDH-CO<sub>2</sub>). The synthesized catalysts were systematically characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N<sub>2</sub> adsorption–desorption isotherm, temperature-programmed desorption of NH<sub>3</sub> and CO<sub>2</sub> (NH<sub>3</sub>/CO<sub>2</sub>-TPD), temperature-programmed reduction of H<sub>2</sub> (H<sub>2</sub>-TPR), and X-ray photoelectron spectroscopy (XPS). It is found that the support can strongly impact on the crystalline phase, the dispersity, and the reduction properties of In<sub>2</sub>O<sub>3</sub>. The catalytic tests during the EBDH-CO<sub>2</sub> show that as compared to In<sub>2</sub>O<sub>3</sub>/MgO and In<sub>2</sub>O<sub>3</sub>/SiO<sub>2</sub> with the merely existence of bulk In<sub>2</sub>O<sub>3</sub> particles, the In<sub>2</sub>O<sub>3</sub>/Al<sub>2</sub>O<sub>3</sub> catalyst gives the highest catalytic activity and good stability, which can be principally ascribed to the synergistic effect of the bulk In<sub>2</sub>O<sub>3</sub> and in situ metallic In formed by the reduction of the well-dispersed In<sub>2</sub>O<sub>3</sub> on the Al<sub>2</sub>O<sub>3</sub> surface. It therefore affirms that attaining an appropriate support to disperse the active phase In<sub>2</sub>O<sub>3</sub> becomes the decisive factor to achieve both superior catalytic activity and satisfied selectivity towards styrene.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 5","pages":"1789 - 1800"},"PeriodicalIF":2.5,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141117660","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}