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Russian Journal of Physical Chemistry A · 2020 ·Vol. 93 ·期 13 ·2613-2619 · IF 0.719

Oxidative Desulfurization Performance of CoAPO-5 Catalysts Synthesized by Novel Dynamic Hydrothermal Method

Xueni Sun,Guan Wenjian,Zheng Jingjing,Zhao Xiangxiang,Wang Jun,Huang Chunxiang,Shao Hui

Abstract CoAPO-5 molecular sieves were synthesized by a novel dynamic method. Crystallization, morphology and surface acidity were investigated by XRD, SEM, and Py-IR in details, and compared with samples prepared by traditional static method. Synthesis conditions, reaction time, temperature and the amount of catalyst were optimized as important parameters. The desulfurization performance of CoAPO-5 catalysts synthesized by two different methods was evaluated and compared. Also, some experiments were carried out to test selectivity and regenerability of CoAPO-5 catalysts synthesized by the dynamic method. Finally, ODS reaction kinetics and mechanism using CoAPO-5 was studied and discussed. Results indicated that dynamic method greatly shortened crystallization time, while kept the same structure and sulfur removal capacity of CoAPO-5. The dynamic synthesis method could be considered as an alternative method to prepare porous molecular sieves.

✓ 已验证 DOI 高影响因子
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TALANTA · 2021 · IF 6.057

A ratiometric fluorescence sensor for 5-hydroxymethylfurfural detection based on strand displacement reaction

Nan Jiang,Peng Li,Shihao Sun,Wei Wei

Since 5-hydroxymethylfurfural (HMF) becomes a neo-forming contaminant with latent harm to human health, development of new method for highly sensitive detection of HMF is extremely desirable. Herein, a novel ratiometric fluorescence sensor based on strand displacement reaction and magnetic separation was designed for sensitive and selective detection of HMF with the help of MnO 2 nanosheets . The aldehyde-functionalized DNA (S0–CHO) and HMF competed for binding to amino-functionalized magnetic beads (NH 2 -MBs). Then, S0–CHO was collected from supernatant by magnetic separation. In the presence of HMF, the obtained S0–CHO induced the formation of T-shaped DNA by strand displacement reaction (SDR), lighting the fluorescence of FAM. In the absence of HMF, no S0–CHO was present to ignite T-shaped DNA. In this situation, fluorescence of Cy5 was turned on. Thus, a ratiometric fluorescence sensor for high-sensitive detection of HMF was developed. The sensor has a wide linear range from 5 nM to 5 μM. It also exhibited high selectivity against other potential interfering substances. It has been successfully applied to analyze HMF in food samples. The method has potential to be expanded to detect other molecules containing aldehyde groups and further be applied in food safety, environment and other fields.

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CHINESE JOURNAL OF CATALYSIS · 2014 · IF 1.552

Selective hydrogenation of D-glucose to D-sorbitol over Ru/ZSM-5 catalysts

Xingcui Guo,Xicheng Wang,Jing Guan,Xiufang Chen,Zhangfeng Qin,Xindong Mu,Mo Xian

Ru particles were introduced into the zeolite ZSM-5 (MFI) by either a conventional impregnation method or a one-step template-free process. The resultant materials were characterized by X-ray diffraction, N 2 adsorption-desorption, scanning electron microscopy, transmission electron microscopy, NH 3 and CO 2 temperature-programmed desorption. The results indicated that the Ru species in ZSM-5 catalysts prepared via the latter approach (designated as Ru/ZSM-5-TF) were highly dispersed in the ZSM-5 framework structure and this material exhibited high catalytic performance during the hydrogenation of D-glucose to D-sorbitol. The conversion of D-glucose was as high as 99.6% with D-sorbitol selectivity reaching 99.2%, exceeding the performance of Ru/ZSM-5 catalysts prepared by the conventional impregnation method with microporous or desilicated ZSM-5 supports. More importantly, this catalyst showed high stability against leaching and poisoning and could be reused several times. The extensive dispersion of the Ru species, strong interaction between the Ru species and the ZSM-5, and the suitable surface acidity-basicity balance of the Ru/ZSM-5-TF were all critical factors leading to excellent catalytic behavior and stability.

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MICROPOROUS AND MESOPOROUS MATERIALS · 2022 · IF 5.876

Cucurbit[5]uril-based porous polymer material for removing organic micropollutants in water

Dan Yang,Xi nan Yang,Ming Liu,Li xia Chen,Qing Li,Hang Cong,Zhu Tao,Xin Xiao

Organic micropollutants pose a tremendous challenge to global water resources, for nonbiodegradable synthetic chemicals, especially. In this investigation, we loaded Cucurbit [5]uril on polymer BPEIH to prepare supramolecular polymer Q[5]@BPEIH with pore structure , which is used to adsorb and remove organic micropollutants in water. The experimental results show that the adsorbent can remove organic micropollutants from water quickly and with high loading, which is better effect than that of traditional activated carbon. In particular, the polymer is an excellent adsorbent for 2,7-dihydroxynaphthalene and Neutral Red pollutants. It also has classy adsorption properties for 1-naphthylamine, Amaranth, Metallic Yellow, 8-hydroxy-1,3,6-trisulfonic acid pyrene, Methyl Orange and Crystal Violet. This adsorbent can also adsorb I 2 . When the adsorption tends to equilibrium, the calculated adsorption rate is 87.2%. These outstanding adsorption effects show that this adsorbent can help to remove a variety of micropollutants in the process of wastewater treatment . More importantly, Q[5]@BPEIH that we designed and synthesized has the characteristics of low synthesis cost, simple synthesis and preparation process, high product yield, fast adsorption speed and strong removal ability. The admirable removal ability of pollutant proved the prospect of Q [5]@BPEIH for rapid sewage disposal.

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Small · 2021 ·Vol. 17 ·期 46 ·2103374 · IF 13.281

Carbon Dots-in-EuAPO-5 Zeolite: Triple-Emission for Multilevel Luminescence Anti-Counterfeiting

Xiaowei Yu,Kaikai Liu,Hongyue Zhang,Bolun Wang,Wenyan Ma,Jiyang Li,Jihong Yu

Multilevel luminescence materials have aroused wide attention for their advanced anti-counterfeiting abilities. However, various complicated stimuli factors involved in multilevel luminescence anti-counterfeiting (MlLA) limit the practical applications of such materials. Herein, carbon dots (CDs) are in situ introduced into Eu-substituted AlPO 4 -5 zeolite (named CDs@EuAPO-5) via a solvent-free thermal crystallization method, which exhibits triple emissions including pink fluorescence mainly associated with Eu 3+ in the zeolite framework, blue fluorescence and green room temperature phosphorescence (RTP) associated with CDs. CDs are uniformly embedded in the EuAPO-5 zeolite matrix. Such composite displays excellent photo-, thermo-, and solvent resistance, as well as long-term storage-stability. Moreover, the triple emissions of the composite only need two kinds of common excitation lights to trigger, without involving other complicated stimuli. A triple-level luminescence anti-counterfeiting (TlLA) label has been built, realizing facile, quick, and advanced luminescence anti-counterfeiting that is hard to copy.

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APPLIED CATALYSIS A-GENERAL · 2018 · IF 4.521

Highly effective transformation of carbohydrates to 5-Hydroxymethylfurfural with Al- montmorillonite as catalyst

Jingjie Cao,Mingwei Ma,Jinchan Liu,Yongquan Yang,Hui Liu,Xingliang Xu,Jiahui Huang,Huijuan Yue,Ge Tian,Shouhua Feng

Aluminum ion-exchanged Ca-montmorillonite with different concentrations of aluminum ion were prepared and applied in the conversion of carbohydrates to 5-hydroxymethylfurfural (HMF). It was found that two types of acid sites were present in the catalyst, Lewis acid sites for isomerization of glucose and Brønsted acid sites for dehydration of fructose. With Al-mont-10 as catalyst, the yield of HMF converted from glucose was 80.4% in a biphase system (THF: NaCl solution) at 180 °C for 2.5 h. Further, the catalyst also shows excellent catalytic performance in the conversion of starch and inulin, and the yield of HMF reached 60.1% and 81.6% under identical conditions, respectively.

✓ 已验证 DOI 高影响因子
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ACS Applied Nano Materials · 2021 · IF 5.097

Co-Crystalline ZSM-5/ZSM-11 Nanostructures for Alkylation of Benzene with Ethanol

Zhongwen Dong,Chuanyu Yang,Dongpu Zhao,Yanan Wang,Weifeng Chu,Zhaochi Feng,Xiangxue Zhu,Wenjie Xin,Yongchen Shang,Shenglin Liu,Longya Xu

The interzeolite transformation approach has been used extensively for the quick synthesis of zeolites at a lower cost. Herein, an interzeolite transformation method for the quick synthesis of co-crystalline ZSM-5/ZSM-11 (CDM-5) nanoaggregates has been developed by precisely controlling the synthesis parameters and using 1,6-hexamethylenediamine as an organic structure-directing agent. In contrast, the irregular CDM-5 zeolite block obtained from an amorphous aluminosilicate gel takes a longer crystallization time using the conventional method. Combined with the related results of characterization, UV-Raman spectra show that double 6-membered rings in the parent USY zeolite framework are broken, and an ordered aluminosilicate aggregate species (OAAS) containing 4-membered rings (4Rs) are formed during the interzeolite transformation. HRTEM and SEM images demonstrate that the block OAAS is dissolved into amorphous nanoparticles, followed by converting into CDM-5 nanoaggregates. These results reveal that an OAAS is essential for the synthesis of CDM-5 nanoaggregates via the interzeolite transformation method. In addition, the CDM-5 nanoaggregate catalyst exhibits superior stability and resistance to carbon deposition in the alkylation reaction of benzene with ethanol compared with the irregular block CDM-5 catalyst.

✓ 已验证 DOI 高影响因子
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SEPARATION AND PURIFICATION TECHNOLOGY · 2019 · IF 5.107

Phosphine oxides functionalized pillar[5]arenes for uranyl extraction: Solvent effect and thermodynamics

Xiangyang Yuan,Yinmin Cai,Lixi Chen,Shihang Lu,Xin Xiao,Lihua Yuan,Wen Feng

As pre-organized multidentate extractants, phosphine oxides functionalized pillar[5]arenes (POP5As) have showed superior efficiency for uranyl extraction. In this work, the effect of type of organic diluents including dichloromethane (DCM), 1,2-dichloroethane (DCE), 1-nitro-3-(trifluoromethyl)benzene (NTFB) and nitropropane (NP) with different polarity and the fundamental thermodynamic behaviour were investigated in the solvent extraction of uranyl by POP5As from nitric acid (1 M) solution. The extraction ability pertaining to spacer length ( C n H 2n , n = 2, 4, 6), diluent polarity and temperature has been evaluated by comparing the distribution coefficients. The extractant with longer spacer exhibited a better performance in all diluents examined. Particularly, influencing factors including structural variation of ligands and property of organic diluents for the extraction efficiency were discussed from the thermodynamic point of view (Δ H , Δ S and Δ G ). Generally, the extraction processes of uranyl by POP5As were exothermic and spontaneous in nature. In the case of DCE , NTFB and NP, Δ H  < 0 and Δ S  < 0, the extraction process of uranyl is enthalpy driven whereas the entropy factor counteracts it. In DCM , Δ H  < 0 and Δ S  > 0, the extraction is synergistically driven by enthalpy and entropy.

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Canadian Journal of Chemistry · 2022 ·Vol. 100 ·期 8 · IF 1.051

Hierarchical ZSM-5 zeolite obtained by designed organosiloxane: synthesis, characterization, and catalytic applications

Changshuai Liu,Rong Zhang,Rujing Pei,Chao Zhang,Fuxiang Li

A new strategy was implemented to synthesize hierarchical ZSM-5 zeolite, which uses self-made organosilanized double-terminal amino polyetheramine (ODAP) as a soft template to generate mesopores. The influence of the additional amount of ODAP on the textural properties and morphologies of the hierarchical ZSM-5 zeolite was investigated. The obtained hierarchical ZSM-5 zeolite was characterized by X-ray diffraction, N2 physical adsorption, SEM, temperature-programmed desorption of NH3, and other methods. The analysis of the experimental results shows that the maximum total BET specific surface area and mesoporous specific surface area of the optimized hierarchical ZSM-5 zeolite reached 609 and 278 m2/g, respectively. Because the synthesized hierarchical ZSM-5 zeolite has a large mesoporous specific surface area and abundant surface acidity, in terms of reactant conversion and product selectivity, compared with microporous zeolite, it exhibits excellent catalytic performance in the thiophene alkylation desulfurization reaction. This synthesis strategy can be extended to the preparation of zeolites with different framework structures, which is of great significance.

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SCRIPTA MATERIALIA · 2013 ·Vol. 69 ·期 8 ·574-577 · IF 2.821

Densification of tantalum carbide ceramics with 5 mol.% Al, Cu, Ag and Au

Limeng Liu,Lianbing Zhong,Baoyou Zhang,Zhonghong Lai,Feng Ye,Zhiguo Zhang,Yu Zhou

The effects of the addition of 5   mol.% aluminum , copper, silver or gold on the densification , microstructures, mechanical properties and oxidation resistance in thin air of TaC ceramics were investigated. Full density and relatively high flexural strength (up to 738   MPa) were observed in the case of the Au addition after spark plasma sintering at 1700   °C for 5   min under 30   MPa pressure. Due to wetting of the TaC grains by a thin metallic film , the consolidated materials showed enhanced oxidation resistance against thin air.

✓ 已验证 DOI 高影响因子
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RSC Advances · 2024 ·Vol. 14 ·期 16 ·11311-11321 · IF 3.9

Controlled delivery of 5-fluorouracil from monodisperse chitosan microspheres prepared by emulsion crosslinking

Tong Wan,Qianqian Zhang,Guocheng Jin,Shiai Xu

This work aims to determine the optimal conditions for emulsion cross-linking of chitosan (CHS) with various molecular weights using glutaraldehyde as a cross-linking agent to produce 5-fluorouracil-loaded CHS microspheres (5-FU/CHS). Their drug loading and encapsulation efficiencies are found to be in the range of 3.87–12.35% and 20.13–70.45%, respectively. The dynamic light scattering results show that 5-FU/CHS microspheres are micron-sized with a uniform size distribution, and the scanning electron microscopy results show that they are spherical. The results of thermogravimetric analysis, X-ray diffraction, and Fourier transform infrared spectroscopy demonstrate that 5-FU is successfully incorporated into the microspheres. The in vitro release tests show that 5-FU/CHS have a prolonged, pH-responsive release pattern of 5-FU, and the cumulative release rate under acidic condition is much larger than that under neutral conditions. The drug release kinetic analysis further demonstrates that the release of 5-FU can be well described by the Fickian diffusion model.

✓ 已验证 DOI PubMed 高影响因子
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Biomass Conversion and Biorefinery · 2025 · IF 4.1

Preparation of 5-hydroxymethylfurfural from cellulose catalyzed by mixed acid: optimization and kinetics

Jia Yu,Liang Xuanyu,Tao Hongge,Chen Binglin,He Chao,Jiao Youzhou,Xu Guizhuan

5-Hydroxymethylfurfural (HMF) is an important platform compound that can be used to synthesize drugs, fine chemicals, fuels, and biodegradable plastics. Synthesis of HMF from cellulose is a key step in the production of high-value-added chemicals and fuels from renewable cellulosic biomass. Herein, a cheap way to produce HMF from cellulose was found in this study. Combination of inexpensive metal salts and inorganic acids shows exciting catalytic efficiency in tetrahydrofuran (THF)/H 2 O system. In this article, the effects of key factors such as water/organic solvent ratio, metal salt type, and concentration on the synthesis of HMF from cellulose were investigated. A maximum HMF yield of 46.5% was obtained with high substrate loading (50 g/L) when H 2 SO 4 and Al 2 (SO 4 ) 3 was used as mixed acid catalysts. Reaction kinetics experiments revealed that combination of H 2 SO 4 and Al 2 (SO 4 ) 3 could effectively reduce the activation energy of cellulose hydrolysis, glucose isomerization, and fructose dehydration compared to the single H 2 SO 4 and single Al 2 (SO 4 ) 3 system. Fortunately, the purity of HMF after separation and purification was up to 98.3%, and both the solvent and the extractant can be recycled. A promising strategy is provided for HMF production from cellulose over simple catalysts.

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