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31.
Selective hydrogenation of benzene to cyclohexene on Ru-basecatalysts promoted with Mn and Zn
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Ru-based catalysts promoted with Mn and Zn were prepared by a co-precipitation method. In liquid-phase hydrogenation of benzene, the Ru-Mn-Zn catalysts exhibited superior catalytic performance to the catalysts promoted with Zn or Mn alone. The optimum Mn/Zn molar ratio was determined to be 0.3. With the addition of 0.5 g NaOH, the Ru-Mn-Zn-0.3 catalyst, which was reduced at 150 ? C, afforded a cyclohexene selectivity of 81.1% at a benzene conversion of 60.2% at 5 min and a maximum cyclohexene yield of 59.9% at 20 min. Based on characterizations, the excellent performance of Ru-Mn-Zn catalyst was ascribed to the suitable pore structure, the appropriate reducibility and the homogenous chemical environment of the catalyst. 相似文献
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Lingling Ran Zhongyi Guo Shiliang Qu 《Applied Physics A: Materials Science & Processing》2010,100(2):517-521
Self-organized periodic surface structures on ZnO have been observed after multiple linearly polarized femtosecond laser pulse
irradiation. The observed self-organized structures are attributed to the second harmonics in the sample surface excited by
the incident laser. The grating orientation could be adjusted by the laser polarization direction. We also find that fluences
play an important role in the formation of self-organized nanostructures. 相似文献
35.
Xiaoli Wu Xulin Cui Wenjia Wu Jingtao Wang Yifan Li Zhongyi Jiang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(51):18695-18700
Lamellar membranes with well‐defined 2D nanochannels show fast, selective permeation, but the underlying molecular transport mechanism is unexplored. Now, regular robust MXene Ti3C2Tx lamellar membranes are prepared, and the size and wettability of nanochannels are manipulated by chemically grafted hydrophilic (?NH2) or hydrophobic (?C6H5, ?C12H25) groups. These nanochannels have a sharp difference in mass transfer behavior. Hydrophilic nanochannels, in which polar molecules form orderly aligned aggregates along channel walls, impart ultrahigh permeance (>3000 L m?2 h?1 bar?1), which is more than three times higher than that in hydrophobic nanochannels with disordered molecular configuration. In contrast, nonpolar molecules with disordered configuration in both hydrophilic and hydrophobic nanochannels have comparable permeance. Two phenomenological transport models correlate the permeance with the mass transport mechanism of molecules that display ordered and disordered configuration. 相似文献
36.
We fabricate F-doped and F-S-codoped diamond-like carbon (DLC) films using plasma-enhanced chemical vapor deposition system. The hardness, Raman spectra, and high-vacuum tribological behaviors indicate that the films are DLC films. The hardness is close related to the tribological properties of DLC films under high vacuum. The high hardness of DLC films would be helpful for obtaining the long lifetime under high vacuum. The lifetimes of F-S-codoped DLC films are about 120 and 140 seconds, which is attributed to the fast graphitization under high vacuum. The lifetime of F-doped DLC films is prolonged to the value of around 300 and 440 seconds, X-ray photoelectron spectroscopy analysis exhibits the existence of the “adsorption” F, and transmission electron microscopy analysis shows that the “adsorption” F could react with Fe to form layered FeF2 nanocrystal at the initial sliding, which could be helpful for prolonging the lifetime of F-doped DLC films under high vacuum. This investigation opens a new window to overcome the disadvantage of F, S-doped DLC films under high vacuum. 相似文献
37.
Linfei Feng Wei Xia Tao Wang Cheng Jiang Hao Gong Bin Gao Zhongyi Jiang Xiao Liu Jianping He 《Journal of Radioanalytical and Nuclear Chemistry》2018,315(3):627-638
The poor structure stability of graphene limits its application as radical scavenger under γ-rays environment because of short service life. Hence we applied polyaniline (PANI), a fairly stable material under irradiation, to modify graphene and then obtained the PANI functionalized graphene oxide (PGO). According to TEM and BET data, the structure stability of PGO is much better than GO after 500 kGy irradiation doses. Electron spin spectroscopy data reveal that PGNS0.10 (PGO/PANI coatings, 0.10 wt%) are not almost affected by adverse influence comes from active radicals. Then PGNS0.10 exhibits the excellent corrosion protection performance after 500 kGy irradiation doses. 相似文献
38.
Yunchuan Pu Mingang Zhao Xu Liang Shaoyu Wang Dr. Hongjian Wang Ziting Zhu Dr. Yanxiong Ren Zhiming Zhang Prof. Guangwei He Prof. Dan Zhao Prof. Zhongyi Jiang 《Angewandte Chemie (International ed. in English)》2023,62(22):e202302355
We report a covalent organic framework (COF) induced seeding strategy to fabricate metal–organic framework (MOF) membranes. Contrary to graphene oxide nuclei-depositing substrate, COF substrate has uniform pore size, high microporosity and abundant functional groups. We designed a series of charged COF nanosheets to induce the formation of ZIF-8@COF nanosheet seeds with high aspect ratio over 150, which were readily processed into a compact and uniform seed layer. The resulting ZIF-8 membranes with thickness down to 100 nm exhibit an ultrahigh C3H6/C3H8 separation performance and superior long-term stability. Our strategy is also validated by fabricating ultrathin ZIF-67 and UiO-66 membranes. 相似文献
39.
Dr. Chi Zhang Dr. Meiling Shao Dr. Dongqing Wu Dr. Zhongyi Li Muzhi Zhao Xiangfei Zhang Prof. Bin Zhai Prof. Yunjun Luo Prof. Xiaoyu Li 《Angewandte Chemie (International ed. in English)》2023,62(52):e202314052
Azide compounds are widely used and especially, polymers bearing pendant azide groups are highly desired in numerous fields. However, harsh reaction conditions are always mandatory to achieve full azidation, causing severe side reactions and degradation of the polymers. Herein, we report the design and preparation of two azide ionic liquids (AILs) with azide anion and triethylene glycol (E3)-containing cation, [P444E3][N3] and [MIME3][N3]. Compared with the traditional sodium azide (NaN3) approach, both AILs showed much higher reaction rates and functional-group tolerance. More importantly, they could act as both reagents and solvents for the quantitative azidation of various polymeric precursors under mild conditions. Theoretical simulations suggested that the outstanding performance of AILs originated from the existence of ion pairs during the reaction, and the E3 moieties played a crucial role. Lastly, after the reaction, the AILs could be easily regenerated, presenting a safer, greener, and highly efficient synthesis route for azide polymers. 相似文献
40.
Biodegradable polymer electrolyte films based on poly(ε-caprolactone) (PCL) in conjunction with lithium tetrafluoroborate (LiBF4) salt and 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIMBF4) ionic liquid were prepared by solution cast technique. The structural, morphological, thermal, and electrical properties of these films were examined using X-ray diffraction (XRD), optical microscopy (OM), differential scanning calorimetry (DSC), and impedance spectroscopy. The XRD and OM results reveal that the pure PCL possesses a semi-crystalline nature and its degree of crystallinity decreases with the addition of LiBF4 salt and EMIMBF4 ionic liquid. DSC analysis indicates that the melting temperature and enthalpy are apparently lower for the 40 wt% EMIMBF4 gel polymer electrolyte as compared with the others. The ambient temperature electrical conductivity increases with increasing EMIMBF4 concentration and reaches a high value of ~2.83?×?10?4 S cm?1 for the 85 PCL:15 LiBF4 + 40 wt% EMIMBF4 gel polymer electrolyte. The dielectric constant and ionic conductivity follow the same trend with increasing EMIMBF4 concentration. The dominant conducting species in the 40 wt% EMIMBF4 gel polymer electrolyte determined by Wagner’s polarization technique are ions. The ionic conductivity of this polymer electrolyte (~2.83?×?10?4 S cm?1) should be high enough for practical applications. 相似文献