共查询到5条相似文献,搜索用时 15 毫秒
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Amorphous Porous Organic Polymers Based on Schiff‐Base Chemistry for Highly Efficient Iodine Capture 下载免费PDF全文
Prof. Dr. Zongxia Guo Panli Sun Xiao Zhang Dr. Jianbin Lin Tong Shi Prof. Dr. Shaofeng Liu Abin Sun Prof. Dr. Zhibo Li 《化学:亚洲杂志》2018,13(16):2046-2053
Porous organic polymers (POPs) have been considered as prominent adsorbents for volatile iodine. So far, both crystalline and amorphous POPs have accomplished excellent iodine capture capability. Considering the difficulty and challenges in preparing perfect crystalline POPs, more explorations into developing versatile amorphous POPs are needed. Herein, amorphous POPs based on the Schiff‐base reaction were designed and synthesized for volatile iodine removal. Four amorphous POPs products named as NDB‐H , NDB‐S , ADB‐HS , and ADB‐S obtained under different solvothermal conditions were investigated in terms of their morphologies, porosity, and their iodine enrichment performance in detail. It is noteworthy that excellent efficiency for removing iodine vapor was acquired for NDB‐S (≈425 wt %), ADB‐HS (≈345 wt %), and ADB‐S (≈342 wt %). Remarkably, NDB‐H exhibited an iodine capture capacity up to ≈443 wt %. Excellent reusability was obtained as well. Amorphous NDB‐H has accomplished an extremely high iodine capture performance, illustrating the great chance to exploit versatile amorphous POPs for iodine enrichment and removal based on Schiff‐base chemistry. 相似文献
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Dr. Zhihua Xu Prof. Jiaguo Yu Dr. Wei Xiao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(29):9592-9598
Mesoporous ferrihydrite/SiO2 composites were synthesized according to a water‐in‐oil microemulsion method and characterized by X‐ray diffraction, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, thermogravimetry, nitrogen‐adsorption/desorption, and by X‐ray photoelectron spectroscopy. The as‐prepared porous ferrihydrite/SiO2 composites showed an excellent adsorption performance for formaldehyde (HCHO) removal from indoor air at ambient temperature. It was found that the aging time during the synthesis had a significant impact on the pore structure, surface area, and HCHO adsorption of these materials. The ferrihydrite/SiO2 composite that was aged for 3 h in the presence of tetraethyl orthosilicate (TEOS) exhibited a relatively high HCHO adsorption capacity, as well as good recyclability, which was attributed to a relatively large BET surface area, optimal pore size, a suitable Si/Fe atomic ratio, and a synergistic effect between ferrihydrite and SiO2. This work not only demonstrates that porous ferrihydrite/SiO2 composites can act as an efficient adsorbent toward HCHO, but suggests a new route for the rational design of cost‐effective and environmentally benign adsorbents with high performance for indoor air purification. 相似文献
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Porous Coordination Polymers of Diverse Topologies Based on a Twisted Tetrapyridylbiaryl: Application as Nucleophilic Catalysts for Acetylation of Phenols 下载免费PDF全文
Saona Seth Prof. Dr. Paloth Venugopalan Prof. Dr. Jarugu Narasimha Moorthy 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(5):2241-2249
Porous coordination polymers (CPs) with partially uncoordinated pyridyl rings based on rationally designed polypyridyl linkers are appealing from the point of view of their application as nucleophilic catalysts. A D2d‐symmetric tetradentate organic linker L , that is, 2,2′,6,6′‐tetramethoxy‐3,3′,5,5′‐tetrakis(4‐pyridyl)biphenyl, was designed and synthesized for metal‐assisted self‐assembly aimed at porous CPs. Depending on the nature of the metal ion and the counter anion, the ligand L is found to function as a 3‐ or 4‐connecting building block leading to porous CPs of diverse topologies. The reaction of L with Zn(NO3)2 and Cd(NO3)2 yields porous 2 D CPs of “ fes ” topology, in which the tetrapyridyl linker L serves as a 3‐connecting unit with its free pyridyl rings well exposed into the pores. The functional utility of these porous CPs containing uncoordinated pyridyl rings is demonstrated by employing them as efficient heterogeneous nucleophilic catalysts for acetylation of a number of phenols with varying electronic properties and reactivities. 相似文献
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Loading of a Coordination Polymer Nanobelt on a Functional Carbon Fiber: A Feasible Strategy for Visible‐Light‐Active and Highly Efficient Coordination‐Polymer‐Based Photocatalysts 下载免费PDF全文
Prof. Dr. Xin‐Xin Xu Dr. Hong‐Yu Yang Dr. Zhen‐Yu Li Prof. Dr. Xiao‐Xia Liu Prof. Dr. Xiu‐Li Wang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(9):3821-3830
To improve the photocatalytic properties of coordination polymers under irradiation in the visible‐light region, coordination polymer nanobelts (CPNB) were loaded on functional carbon fiber (FCF) through the use of a simple colloidal blending process. The resulting coordination polymer nanobelt loaded functional carbon fiber composite material (CPNB/FCF) exhibited dramatically improved photocatalytic activity for the degradation of rhodamine B (RhB) under visible‐light irradiation. Optical and electrochemical methods illustrated the enhanced photocatalytic activity of CPNB/FCF originated from high separation efficiency of photogenerated electrons and holes on the interface of CPNB and FCF, which was produced by the synergy effect between them. In the composite material, the role of FCF could be described as photosensitizer and good electron transporter. For FCF, the number of functional groups on its surface has a significant influence on the photocatalytic performance of the resulting CPNB/FCF composite material, and an ideal FCF carrier was obtained as a highly efficient CPNB/FCF photocatalyst. CPNB/FCF showed outstanding stability during the degradation of rhodamine B (RhB); thus, the material is suitable for use as a photocatalyst in the treatment of organic dyes in water. 相似文献