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Highly selective capture of SO2 with supported micro-mesoporous silica sphere from CO2-rich environment SCIE
期刊论文 | 2024 , 436 | JOURNAL OF CLEANER PRODUCTION
WoS CC Cited Count: 1
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Abstract :

Selective adsorption of sulfur dioxide (SO2) is an important clean technology for purification of exhaust gas from fossil fuel combustion. The widely applied zeolite-based adsorbents interact with SO2 through weakly physical adsorption, resulting in low adsorption capacity and selectivity for SO2. Herein, a facile strategy that combines improving the textural property of zeolite and optimizing adsorption sites is developed for efficient and stable SO2 adsorption. The micro-mesoporous silica sphere (MS) with high specific surface area and well-defined pore structure is obtained through a micelle expander assisted soft-template method, which can facilitate the dispersion and exposure of designed adsorption sites- methylated polyethyleneimine (mPEI). Since the Lewis basic sites of N in mPEI can strongly interact with the pi-receptor SO2, and the tertiary amine groups exhibit a weak attraction for CO2, the optimized MS supported mPEI adsorbent exhibits remarkable SO2 adsorption performance (7.5 mmol/g), exceptionally high SO2/N2 selectivity (16673) and SO2/CO2 selectivity (551). Moreover, it presents an outstanding stability in the adsorption-regeneration test. This work sheds light on the design of high-performance organic-solid composite adsorbent for selective capture of SO2.

Keyword :

Adsorption Adsorption Micro-mesoporous silica sphere Micro-mesoporous silica sphere Polytertiary amine Polytertiary amine Selective desulfurization Selective desulfurization SO 2 capture SO 2 capture

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GB/T 7714 Zhang, Qiongdan , Wei, Jixiang , Gao, Changbo et al. Highly selective capture of SO2 with supported micro-mesoporous silica sphere from CO2-rich environment [J]. | JOURNAL OF CLEANER PRODUCTION , 2024 , 436 .
MLA Zhang, Qiongdan et al. "Highly selective capture of SO2 with supported micro-mesoporous silica sphere from CO2-rich environment" . | JOURNAL OF CLEANER PRODUCTION 436 (2024) .
APA Zhang, Qiongdan , Wei, Jixiang , Gao, Changbo , Zheng, Yong , Xiao, Yihong , Liu, Fujian et al. Highly selective capture of SO2 with supported micro-mesoporous silica sphere from CO2-rich environment . | JOURNAL OF CLEANER PRODUCTION , 2024 , 436 .
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Facilely tuning the morphologies of tertiary amine-functionalized SBA-15 for optimizing selective SO 2 capture SCIE
期刊论文 | 2024 , 487 | CHEMICAL ENGINEERING JOURNAL
WoS CC Cited Count: 3
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Abstract :

The amine -based materials pose high potential for the adsorption of sulfur dioxide (SO 2 ). This work is aimed at modulating the morphologies of SBA -15 adsorbents by controlling the precursor self -assembly processes, for the sake of optimizing the utilization efficiency of amine species in the polytertiary amine (PTA)-functionalized SBA15. It results that worm -like SBA -15 (WLS) material shows a better particle aspect ratio and well-defined pore structure, which helps to optimize the adsorption sites invoked by the preferable dispersion and exposure of PTA, thus amplifying the chemisorption of SO 2 on the adsorbent. Consequently, the functionalized WLS-PTA adsorbent exhibits remarkable SO 2 adsorption performance (15.43 mmol/g), exceptionally high selectivities of SO 2 /N 2 (27522) and SO 2 /CO 2 (652). Surprisingly, the desulfurization capacity can be further enhanced by the positive effect of the water vapor co -fed. It is unveiled that the whole SO 2 adsorption process mainly follows the dual site Langmuir-Freundlich isotherm model and Bangham model. This work sheds light on the design of polymer -solid composite adsorbents for selective capture of SO 2 .

Keyword :

Mesoporous SBA-15 Mesoporous SBA-15 Polytertiary amine Polytertiary amine Selective desulfurization Selective desulfurization SO2 adsorption SO2 adsorption Solid amine adsorbent Solid amine adsorbent

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GB/T 7714 Zhang, Qiongdan , Lei, Yuanyi , Ye, Ming et al. Facilely tuning the morphologies of tertiary amine-functionalized SBA-15 for optimizing selective SO 2 capture [J]. | CHEMICAL ENGINEERING JOURNAL , 2024 , 487 .
MLA Zhang, Qiongdan et al. "Facilely tuning the morphologies of tertiary amine-functionalized SBA-15 for optimizing selective SO 2 capture" . | CHEMICAL ENGINEERING JOURNAL 487 (2024) .
APA Zhang, Qiongdan , Lei, Yuanyi , Ye, Ming , Wang, Heng , Zheng, Yong , Xiao, Yihong et al. Facilely tuning the morphologies of tertiary amine-functionalized SBA-15 for optimizing selective SO 2 capture . | CHEMICAL ENGINEERING JOURNAL , 2024 , 487 .
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Promoting methane combustion activity and stability by tuning multiple Ni-Si interactions in catalysts SCIE
期刊论文 | 2023 , 349 | FUEL
WoS CC Cited Count: 9
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Abstract :

Catalytic combustion holds great promise for eliminating unburned methane released by the natural gas industry, and the crucial factor is the development of cost-effective and efficient catalysts. Herein, the silicon component was introduced into nickel oxide by simultaneously regulating the precipitation of nickel precursors and the hydrolysis of silicon precursors. The generation of SiO4 groups in NiO inhibited the growth and sintering of NiO grains, meanwhile promoting the formation of active Ni2+ and adsorbed oxygen species for activation and oxidation of methane. With the increase of Si content, the existence of surface nickel silicate on NiO further improved the sinter resistance of NiO, but caused the diminish of Ni2+ and surface adsorbed oxygen species. The catalytic activity and stability were co-enhanced via facilely tuning the multiple Ni-Si interactions. The catalyst with abundant SiO4 groups and negligible nickel silicate exhibited considerably higher catalytic activity, sinter-resistance and water-resistance than NiO toward methane combustion.

Keyword :

Catalytic activity Catalytic activity Methane combustion Methane combustion Multiple Ni-Si interaction Multiple Ni-Si interaction NiO-based catalysts NiO-based catalysts Thermal stability Thermal stability

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GB/T 7714 Wang, Zhixiong , Tang, Chenyao , Lin, Jia et al. Promoting methane combustion activity and stability by tuning multiple Ni-Si interactions in catalysts [J]. | FUEL , 2023 , 349 .
MLA Wang, Zhixiong et al. "Promoting methane combustion activity and stability by tuning multiple Ni-Si interactions in catalysts" . | FUEL 349 (2023) .
APA Wang, Zhixiong , Tang, Chenyao , Lin, Jia , Zheng, Yong , Xiao, Yihong , Zheng, Ying et al. Promoting methane combustion activity and stability by tuning multiple Ni-Si interactions in catalysts . | FUEL , 2023 , 349 .
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Ce-Mn Oxide Nanocomposites for Catalytic Removal of H2S SCIE
期刊论文 | 2023 , 6 (4) , 2585-2595 | ACS APPLIED NANO MATERIALS
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Abstract :

The development of efficient and stable nanocatalysts is crucial for the catalytic removal of H2S through selective oxidation to sulfur. Inspired by the different catalytic activity and selectivity of CeO2 and MnO2 for the reaction, cerium-manganese (Ce-Mn) nanocomposite oxides with tunable phase structure and unique surface properties were constructed to optimize the catalytic performance. By regulating the molar ratio of Ce and Mn components, a novel catalyst structure comprising Ce-Mn solid solution and amorphous CeO2 is synthesized from Ce-Mn oxide with n(Ce)/n(Mn) ratio of 0.5 (50Ce-Mn). Compared with the unmodified MnO2, the tailored 50Ce-Mn possesses a high specific surface area, which facilitates the access of reactants to active sites and the desorption of formed sulfur. More importantly, strong Ce-Mn interaction and abundant surface-active oxygen species are generated, contributing to the regeneration of Mn4+/Ce4+ active sites, facilitating the formation of sulfur, and inhibiting the accumulation of sulfates during the reaction. Consequently, 50Ce-Mn presents a superior catalytic activity (T-100 of 150 degrees C), stability, and sulfur selectivity even under relatively high weight hourly space velocity conditions (23,000 mL center dot g(-1)center dot h(-1)). This study provides an example of how catalytic performance can be boosted through phase structure regulation on nanocomposites.

Keyword :

cerium-manganese nanocatalysts cerium-manganese nanocatalysts electron transfer electron transfer H2S-selective catalytic oxidation H2S-selective catalytic oxidation oxygen vacancy oxygen vacancy phase structure phase structure

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GB/T 7714 Zhang, Qiongdan , Zheng, Chengcheng , Zhang, Ke et al. Ce-Mn Oxide Nanocomposites for Catalytic Removal of H2S [J]. | ACS APPLIED NANO MATERIALS , 2023 , 6 (4) : 2585-2595 .
MLA Zhang, Qiongdan et al. "Ce-Mn Oxide Nanocomposites for Catalytic Removal of H2S" . | ACS APPLIED NANO MATERIALS 6 . 4 (2023) : 2585-2595 .
APA Zhang, Qiongdan , Zheng, Chengcheng , Zhang, Ke , Zheng, Yong , Xiao, Yihong , Jiang, Lilong . Ce-Mn Oxide Nanocomposites for Catalytic Removal of H2S . | ACS APPLIED NANO MATERIALS , 2023 , 6 (4) , 2585-2595 .
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Controllable creating mesoporous coordination unsaturated sites in UiO-66 single crystals for efficient conversion of hydrogen sulfide into polysulphur SCIE
期刊论文 | 2023 , 479 | CHEMICAL ENGINEERING JOURNAL
WoS CC Cited Count: 4
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Abstract :

We report herein a facile pyrolysis etching strategy for the fabrication of UiO-66-xs single crystals with tunable coordination unsaturated zirconium sites (Zr-CUS) as well as interconnected mesoporosity. The synthesis is realized by having pristine UiO-66-xs subjected to thermal treatment, which results in the selective decompo-sition of thermal-sensitive organic linkers and hence the creation of permanent mesoporosity, leaving abundant Zr-CUS with enhanced degree of exposure. The prepared hierarchically porous UiO-66-xs (HP-UiO-66-xs) were innovatively applied for mild oxidation of H2S into polysulphur, achieving near 100 % H2S conversion and polysulphur selectivity in a wide range of temperatures. The superior activities can be well maintained in a continuous test of over 50 h. The Zr-CUS of HP-UiO-66-xs effectively activate H2S and O2 via the "adsorption dissociation tandem hydrogen transfer" mechanism, and the abundant mesochannels ensure efficient transport of reactants and bulky products in and out HP-UiO-66-xs, leading to catalytic activities superior to those of traditional H2S selective oxidation catalysts.

Keyword :

Coordination unsaturated degree Coordination unsaturated degree H2S selective oxidation H2S selective oxidation Mass transportation Mass transportation Mesoporous metal organic frameworks Mesoporous metal organic frameworks Polysulphur catalytic synthesis Polysulphur catalytic synthesis

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GB/T 7714 Zhang, Guanqing , Liu, Fengqing , Qu, Yongfang et al. Controllable creating mesoporous coordination unsaturated sites in UiO-66 single crystals for efficient conversion of hydrogen sulfide into polysulphur [J]. | CHEMICAL ENGINEERING JOURNAL , 2023 , 479 .
MLA Zhang, Guanqing et al. "Controllable creating mesoporous coordination unsaturated sites in UiO-66 single crystals for efficient conversion of hydrogen sulfide into polysulphur" . | CHEMICAL ENGINEERING JOURNAL 479 (2023) .
APA Zhang, Guanqing , Liu, Fengqing , Qu, Yongfang , Zheng, Yong , Cao, Yanning , Liu, Fujian et al. Controllable creating mesoporous coordination unsaturated sites in UiO-66 single crystals for efficient conversion of hydrogen sulfide into polysulphur . | CHEMICAL ENGINEERING JOURNAL , 2023 , 479 .
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一种硫化氢选择性氧化催化剂及其制备方法和应用 incoPat
专利 | 2022-03-12 00:00:00 | CN202210239764.0
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Abstract :

本发明属于材料制备及环境催化的技术领域,具体涉及一种硫化氢选择性氧化催化剂及其制备方法和应用。催化剂铈锰复合金属氧化物(Ce‑MnO2)是通过KMnO4添加铈盐和还原沉淀剂反应制备。在高锰酸钾和铈盐混合均匀的水溶液中缓慢加入还原沉淀剂,再经过搅拌、水热、分离、干燥和焙烧得到铈改性二氧化锰催化剂。本发明提供方法制备的铈改性二氧化锰催化剂比表面积大,应用于H2S的选择性催化氧化反应中,表现出高H2S转化率和硫选择性,并具有较好的稳定性。

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GB/T 7714 肖益鸿 , 郑程程 , 杨勤丰 et al. 一种硫化氢选择性氧化催化剂及其制备方法和应用 : CN202210239764.0[P]. | 2022-03-12 00:00:00 .
MLA 肖益鸿 et al. "一种硫化氢选择性氧化催化剂及其制备方法和应用" : CN202210239764.0. | 2022-03-12 00:00:00 .
APA 肖益鸿 , 郑程程 , 杨勤丰 , 郑勇 , 曹彦宁 , 刘福建 et al. 一种硫化氢选择性氧化催化剂及其制备方法和应用 : CN202210239764.0. | 2022-03-12 00:00:00 .
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一种逆流整体式催化燃烧与吸热反应耦合的反应系统 incoPat
专利 | 2022-04-15 00:00:00 | CN202210396416.4
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本发明提出一种逆流整体式催化燃烧与吸热反应耦合的反应系统,所使用的整体式催化燃烧‑吸热反应耦合反应器呈竖向的柱形体,其底端处设有可燃气体入口,顶部设有原料气入口,柱形体内整体式催化燃烧固定反应床与吸热反应床均呈环形柱状,两者的环层以交替套叠方式形成套层耦合结构;可燃气体经第二换热器预热至催化燃烧反应温度后,进入整体式催化燃烧固定反应床环层燃烧并加热吸热反应床环层,其燃烧尾气返回第二换热器作为热源冷却后排出;所述原料气经第一换热器预热后进入吸热反应床环层进行反应,其气态反应产物经吸热反应床的产物出口返回第一换热器作为热源冷却后输入收集装置储存;本发明能够将低浓度可燃气体治理与吸热反应相互结合。

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GB/T 7714 蔡国辉 , 王智雄 , 林立 et al. 一种逆流整体式催化燃烧与吸热反应耦合的反应系统 : CN202210396416.4[P]. | 2022-04-15 00:00:00 .
MLA 蔡国辉 et al. "一种逆流整体式催化燃烧与吸热反应耦合的反应系统" : CN202210396416.4. | 2022-04-15 00:00:00 .
APA 蔡国辉 , 王智雄 , 林立 , 罗宇 , 陈崇启 , 肖益鸿 et al. 一种逆流整体式催化燃烧与吸热反应耦合的反应系统 : CN202210396416.4. | 2022-04-15 00:00:00 .
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二氧化钛-氧化铝复合脱硫催化剂及其制备方法和应用 incoPat
专利 | 2022-03-24 00:00:00 | CN202210296118.8
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本发明公开了一种二氧化钛‑氧化铝复合脱硫催化剂及其制备方法和应用。所述催化剂采用溶胶凝胶法,加入适当浓度的碱性化合物调节溶液的pH,经过一段时间陈化后离心、洗涤、干燥、煅烧得到二氧化钛‑氧化铝催化剂,用于催化羰基硫水解反应。该发明至少由如下原料得到:铝源,所述铝源包括但不限于硝酸铝、氯化铝和异丙醇铝;钛源,所述钛源包括但不限于钛酸四丁酯、四氯化钛、硫酸氧钛,所述钛离子的添加量为金属离子总摩尔数量的0~0.1。本发明制备出复合材料脱硫催化剂,其制备工艺简单,无须浸渍其他活性组分可直接作为催化剂,可在复杂氛围下有效催化羰基硫水解反应,并具有良好的稳定性。

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GB/T 7714 肖益鸿 , 杨勤丰 , 郑程程 et al. 二氧化钛-氧化铝复合脱硫催化剂及其制备方法和应用 : CN202210296118.8[P]. | 2022-03-24 00:00:00 .
MLA 肖益鸿 et al. "二氧化钛-氧化铝复合脱硫催化剂及其制备方法和应用" : CN202210296118.8. | 2022-03-24 00:00:00 .
APA 肖益鸿 , 杨勤丰 , 郑程程 , 郑勇 , 曹彦宁 , 刘福建 et al. 二氧化钛-氧化铝复合脱硫催化剂及其制备方法和应用 : CN202210296118.8. | 2022-03-24 00:00:00 .
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一种无溶剂化制备Fe掺杂介孔磷酸钛脱硫催化剂的方法 incoPat
专利 | 2022-05-30 00:00:00 | CN202210599194.6
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本发明公开了一种Fe掺杂介孔磷酸钛的无溶剂化制备方法及其在催化H2S选择性氧化中的应用,其是将钛源、磷源、铁盐、模板剂、盐酸、醋酸通过机械搅拌实现均匀混合后,经热处理、煅烧制得结构稳定的Fe掺杂介孔磷酸钛。本发明合成方法简单,耗时短,制备过程中不需加入溶剂,原子利用率高,无任何废液产生,且所得材料在催化H2S选择性氧化性能测试中展现出高的催化活性和选择性,其在180℃下具有高达100%的H2S转化率,对S的选择性达80%以上,在稳定性测试中其催化活性能维持50 h以上,适用于中低温催化氧化H2S气体。

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GB/T 7714 刘福建 , 肖淑英 , 江莉龙 et al. 一种无溶剂化制备Fe掺杂介孔磷酸钛脱硫催化剂的方法 : CN202210599194.6[P]. | 2022-05-30 00:00:00 .
MLA 刘福建 et al. "一种无溶剂化制备Fe掺杂介孔磷酸钛脱硫催化剂的方法" : CN202210599194.6. | 2022-05-30 00:00:00 .
APA 刘福建 , 肖淑英 , 江莉龙 , 郑勇 , 曹彦宁 , 肖益鸿 . 一种无溶剂化制备Fe掺杂介孔磷酸钛脱硫催化剂的方法 : CN202210599194.6. | 2022-05-30 00:00:00 .
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一种在线装卸料固定床填料塔 incoPat
专利 | 2023-04-26 00:00:00 | CN202320979996.X
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本实用新型公开了一种在线装卸料固定床填料塔,在其一端设有进气口,另一端设有出气口,填料塔内设有多个分隔板,每个分隔板上分别设置一通孔,分隔板将填料塔的内腔分隔为进气腔和若干个填料吸附腔,每个填料吸附腔中安装有环形填料层,环形填料层安装在分隔板的远离进气口的一侧面,环形填料层的中部形成一进气通道,进气通道的一端与通孔连通,其另一端密封,环形填料层的外侧与填料塔的内侧面形成一环腔,环腔与其相邻的下一个填料吸附腔中的环形填料层的进气通道相连通。本实用新型在环形填料层中采用径向独立通气方式,其通气面积大,阻力小,且与同等通气面积的轴向吸附塔相比,占地面积小,且压力降小,适用于填料需通过大幅变温的工况。

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GB/T 7714 江莉龙 , 郑勇 , 曹彦宁 et al. 一种在线装卸料固定床填料塔 : CN202320979996.X[P]. | 2023-04-26 00:00:00 .
MLA 江莉龙 et al. "一种在线装卸料固定床填料塔" : CN202320979996.X. | 2023-04-26 00:00:00 .
APA 江莉龙 , 郑勇 , 曹彦宁 , 刘时球 , 肖益鸿 . 一种在线装卸料固定床填料塔 : CN202320979996.X. | 2023-04-26 00:00:00 .
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