Molecular Catalysis
·
2022
·
IF 5.089
Zhiquan Yu,Yan Li,Yunlong Yao,Yao Wang,Ying-Ya Liu,Zhichao Sun,Chuan Shi,Wei Wang,Anjie Wang
A bifunctional Ni 3 P/γ-Al 2 O 3 catalyst with both metal site and Lewis acid site was prepared by an electroless plating method, and applied in hydrogenative ring-rearrangement of furfural to cyclopentanone. The obtained catalyst was characterized by XRD, XPS, XAS, N 2 adsorption-desorption, ICP, TEM, CO chemisorption, NH 3 -TPD and Py-FTIR. The ultrafine Ni 3 P nanoparticles (∼3.8 nm) were highly dispersed in the catalyst. The exclusive Lewis acidity of Ni 3 P/γ-Al 2 O 3 was beneficial for the aqueous-phase hydrogenative ring-rearrangement. The effects of DP time, reaction parameters (temperature, H 2 pressure, solvent composition, and reaction time) on the catalytic performance were investigated. The yield of cyclopentanone was 74.6% at furfural conversion of 99.9% at 180 °C in 1 h over Ni 3 P/γ-Al 2 O 3 catalyst using pure water as the solvent. Moreover, the kinetics of hydrogenative ring-rearrangement of furfural catalyzed by Ni 3 P/γ-Al 2 O 3 was investigated.
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
·
2022
·Vol. 23
·期 12
·6597
·
IF 6.208
Yaowei Guo,Jin Liu,Qinglin Tang,Cuicui Li,Yanying Zhang,Yao Wang,Yanxin Wang,Yupeng Bi,Christopher D. Snow,Matt J. Kipper,Laurence A. Belfiore,Jianguo Tang
The clinical use of anticancer drugs necessitates new technologies for their safe, sensitive, and selective detection. In this article, lanthanide (Eu3+and Tb3+)-loaded γ-cyclodextrin nano-aggregates (ECA and TCA) are reported, which sensitively detects the anticancer drug irinotecan by fluorescence intensity changes. Fluorescent lanthanide (Eu3+and Tb3+) complexes exhibit high fluorescence intensity, narrow and distinct emission bands, long fluorescence lifetime, and insensitivity to photobleaching. However, these lanthanide (Eu3+and Tb3+) complexes are essentially hydrophobic, toxic, and non-biocompatible. Lanthanide (Eu3+and Tb3+) complexes were loaded into naturally hydrophilic γ-cyclodextrin to form fluorescent nano-aggregates. The biological nontoxicity and cytocompatibility of ECA and TCA fluorescent nanoparticles were demonstrated by cytotoxicity experiments. The ECA and TCA fluorescence nanosensors can detect irinotecan selectively and sensitively through the change of fluorescence intensity, with detection limits of 6.80 μM and 2.89 μM, respectively. ECA can safely detect irinotecan in the cellular environment, while TCA can detect irinotecan intracellularly and is suitable for cell labeling.Keywords:lanthanide (Eu3+, Tb3+) complex;γ-cyclodextrin;nano-aggregate;sensing;anticancer drug;irinotecan
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Catalysts
·
2022
·Vol. 12
·期 7
·716
·
IF 4.501
Xinbo Zhu,Xiqiang Wu,Jin Liu,Jianbin Luo,Zhengda Yang,Ye Jiang,Geng Chen
In this work, soot oxidation was conducted over a series of Mn-X/γ-Al2O3(M = Ce, Co and Cu) binary catalysts in a dielectric barrier discharge reactor. The soot conversion in the plasma–catalytic system was in the order of Mn/γ-Al2O3(57.7%) > Mn-Co/γ-Al2O3(53.9%) > Mn-Ce/γ-Al2O3(51.6%) > Mn-Cu/γ-Al2O3(47.7%) during the 30 min soot oxidation process at 14 W and 150 °C. Meanwhile, the doping of Ce, Co and Cu slightly improved the CO2selectivity of the process by 4.7% to 10.3% compared to soot oxidation over Mn/γ-Al2O3.It is worth to note that the order of CO2selectivity was in the opposite order with soot oxidation rate. The effects of discharge power, oxygen content in the carrier gas and reaction temperature on plasma–catalytic soot oxidation was systematically analyzed. The catalyst characterizations, including N2adsorption–desorption, X-ray diffraction, X-ray photoelectron spectroscopy, temperature-programmed reduction by H2and temperature-programmed desorption of O2,were conducted to illustrate the reaction mechanisms of plasma–catalytic soot oxidation and reaction pathways.Keywords:plasma–catalysis;soot oxidation;manganese-based oxides;transition metal;binary catalyst
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RSC Advances
·
2022
·Vol. 12
·期 36
·23118-23128
·
IF 4.036
Luxin Zhang,Xu Xing,Ruijun Sun,Meng Hu
Selective catalytic conversion of carbohydrates to 5-ethoxymethylfurfural (EMF) is a critical approach to the biorefinery. In this work, solid acid catalysts of γ-AlOOH and CeO2@B2O3 were used to convert carbohydrates to EMF in a one-pot process, performed in an ethanol/DMSO solvent system. The synergistic effect of γ-AlOOH and CeO2@B2O3 was studied. Furthermore, the morpho-structural properties of the catalysts were characterized, and the effects of reaction time, reaction temperature, catalyst load, and the amount of cosolvent on the conversion of glucose to EMF were examined and optimized. Under the reaction conditions of 170 °C for 20 h, glucose, sucrose, cellobiose, inulin and starch were used as raw materials, and the EMF yield range was 9.2–27.7%. The results showed that the synergistic effect of γ-AlOOH and CeO2@B2O3 further causes the combination of multiple acid sites with different types and strength distributions. Particularly, the collaboration between weak, medium-strong, and strong acid, as well as between Lewis and Brønsted acidity, is of great significance for EMF generation. The reusability experiments showed that the combined catalytic system was easily separated and maintained catalytic activity for five successive reactions without further intermediate regeneration steps. This work provides a promising route for the catalytic conversion of biomass-derived carbohydrates into EMF.
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MICROPOROUS AND MESOPOROUS MATERIALS
·
2021
·
IF 5.455
Haibiao Yu,Xiu Jia,Peng Wang,Ying Xiong,Weijun Shan,Congge Zhang,Zhimeng Song
A series of x wt%Al-SBA-15 catalysts prepared by modified wetness impregnation was investigated for γ-valerolactone (GVL) decarboxylation to butene . It was found that the impregnation of Al species not only remained the ordered mesoporous structure of parent SBA-15, but also created large amounts of Brønsted and Lewis acid sites on the surface of catalyst. The considerable amount of solid acid sites and the suitable Brønsted/Lewis acid ratio endowed 2.23 wt%Al-SBA-15 catalyst an excellent catalytic performance. Under the optimized conditions, the GVL conversion and butene yield can reach 99.8% and 96.6% at 320 °C, respectively. Mechanism studies indicated that the decarboxylation of γ-protonated PEA controlled speed of the whole reaction. Moreover, the catalytic activity of regenerated 2.23 wt%Al-SBA-15 catalyst was satisfactory after eight cycle tests, and the butene yield could still reach 92.2%.
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CARBOHYDRATE POLYMERS
·
2021
·
IF 9.381
Penghui Wang,Yajie Pu,Yanhan Ren,Rong Yang,Wenjie Zhang,Xiaoyan Tan,Wenliang Xue,Shuai Liu,Shuang Li,Bo Chi
Traditional hydrogels often fail to match the dynamic interactions between mechanical and cellular behaviors exhibited by the natural cartilage extracellular matrix. In this research, we constructed a novel hybrid hydrogels system based on sodium alginate and polyglutamic acid. By controlling the grafting rate and concentration of polymer, the gelation time and mechanical strength can be adjusted between range of 8–28 s and 60–144 kPa. By adding microcrystalline cellulose into the system, so that the degradation time was prolonged (125%) and the swelling rate was reduced (470%). Additionally, the presence of hydrazone bonds gives the system some dynamic response characteristics, and the hydrogel exhibits excellent self healing and injectable ability. It was found that the system had positive cytocompatibility (80%), which accelerated regulatory gene expression in cartilage tissue. In conclusion, this injectable hydrogel with self-healing and customizable mechanical strength will have broad application prospects in future biomedical engineering.
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RSC Advances
·
2021
·Vol. 12
·期 1
·602-610
·
IF 3.361
Yingxin Liu,Kai Liu,Meihua Zhang,Kaiyue Zhang,Jiao Ma,Shuwen Xiao,Zuojun Wei,Shuguang Deng
Highly active and thermally stable Cu–Re bimetallic catalysts supported on TiO2 with 2.0 wt% loading of Cu were prepared via an incipient wetness impregnation method and were applied for liquid phase selective hydrogenation of levulinic acid (LA) to γ-valerolactone (GVL) in H2. The effect of the molar ratios of Cu : Re on the physico-chemical properties and the catalytic performance of the Cu–Re/TiO2 catalysts was investigated. Moreover, the influence of various reaction parameters on the hydrogenation of LA to GVL was studied. The results showed that the Cu–Re/TiO2 catalyst with a 1 : 1 molar ratio of Cu to Re (Cu–Re(1 : 1)/TiO2) exhibited the highest performance for the reaction. Complete conversion of LA with a 100% yield of GVL was achieved in 1,4-dioxane solvent under the reaction conditions of 180 °C, 4.0 MPa H2 for 4 h, and the catalyst could be reused at least 6 times with only a slight loss of activity. Combined with the characterization results, the high performance of the catalyst was mainly attributed to the well-dispersed Cu–Re nanoparticles with a very fine average size (ca. 0.69 nm) and the co-presence of Cu–Re bimetal and ReOx on the catalyst surface.
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SURFACE & COATINGS TECHNOLOGY
·
2021
·
IF 4.158
Lei Dai,Tingting Wang,Boxuan Jin,Na Liu,Yifei Niu,Wenhao Meng,Ziming Gao,Xianwen Wu,Ling Wang,Zhangxing He
Zinc is a widely used anode material for zinc-ion batteries. However, the problems of dendrites and side reactions faced by the metal zinc anode limit its cycle stability and service life. Surface modification is a simple and effective strategy for preparing high-performance anodes. Here, we used a simple method to coat the γ-Al 2 O 3 on surface of metal zinc as an artificial protective layer for the anode/electrolyte. γ-Al 2 O 3 coating can guide the uniform deposition of zinc ions . The coating has good hydrophilicity, which is conducive to accelerate ion transmission. In addition, the importance of controlling the thickness of protective layer on surface of zinc metal anode to obtain good electrochemical performance is emphasized. The appropriate thickness of Al 2 O 3 coating ensures the rapid migration of zinc ions and improves the uniformity of zinc plating/stripping, which is conducive to more uniform zinc nucleation and high-quality deposition. Therefore, the discharge capacity of Zn@Al 2 O 3 -15 full cell at a current density of 0.3 A g −1 is 174.3 mAh g −1 , which is much higher than that of bare zinc cell (71.8 mAh g −1 ). This work has certain reference significance for the development of anode coating strategies in zinc-ion batteries.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2020
·
IF 16.683
Shanhui Zhu,Huan Liu,Sen Wang,Xiaoqing Gao,Pengfei Wang,Jianguo Wang,Weibin Fan
One-step efficient conversion of cellulose into value-added γ-valerolactone (GVL) is of great interest because it not only integrates complex tandem reactions in one-step, but also does not need additional hydrogen sources. To achieve this goal, it is crucial to fabricate high-performance catalyst that can accelerate both hydrolysis of cellulose and further transformation of generated stoichiometric levulinic acid (LA) and formic acid (FA) into GVL. CoNi nanoparticles encapsulated in N-doped thin graphene shell gave GVL yield as high as 55.9 % at 200 °C combined with Ag + -exchanged heteropolyacid (AgPW). This composite catalyst is highly resistant to the corrosion of LA and FA, and hence shows high catalytic stability. LA-adsorption FTIR spectra and DFT calculations indicate that LA and FA can penetrate through shell graphene layers into core CoNi sites via cracks. Compared to H 2 , FA can much more rapidly reduce LA because of its low dissociation energy barrier and high dissociation rate.
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Journal of Materials Chemistry B
·
2020
·Vol. 9
·期 7
·1867-1876
·
IF 5.344
Man Luo,Fujian Zhao,Lu Liu,Zhen Yang,Ting Tian,Xiaoyu Chen,Xiaodong Cao,Dafu Chen,Xiaofeng Chen
The macrophage-dominated bone immune response plays an important role in osteogenesis of bone defects. Generally, M2 macrophages are beneficial to promote osteogenesis. However, recent studies have confirmed that M1 also plays an important role in early angiogenesis, osteointegration. Therefore, achieving sequential polarization of macrophages from M1 to M2 may be more beneficial for osteogenesis. In this study, a new type of bone immunomodulatory IFN-γ/Sr-dropped bioactive glass composite scaffold (IFN-γ/SrBG) was successfully prepared which integrates multiple biological functions at different stages of the bone healing process. The scaffold can polarize macrophages into pro-inflammatory M1 type at the early stage of implantation by releasing IFN-γ within the first day, and then polarize macrophages into anti-inflammatory M2 type at a later stage by releasing Sr2+ from SrBG, which promoted mature bone formation in bone defects to a greater extent. Therefore, IFN-γ/SrBG scaffolds are expected to become excellent bone tissue engineering materials by sequential regulation of macrophage polarization.
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高影响因子
BULLETIN OF MATERIALS SCIENCE
·
2020
·Vol. 43
·期 1
·1-7
·
IF 1.392
Xiao Meng,Peng Yu,Pang Mengting,Hao Baicun,Wang Yujia,Zhang Yulian,Liao Yang,Mao Hui
Heterogeneous Pd catalysts were developed by immobilizing Pd nanoparticles (Pd NPs) onto plant polyphenol (bayberry tannin, BT) decorated γ-Al 2 O 3 . The abundant hydroxyls of plant polyphenols were capable of stabilizing the Pd NPs. Transmission electron microscopy observation confirmed that the Pd NPs with the diameter of 3.75 ± 0.5 nm were highly dispersed in the catalyst. The as-prepared Al 2 O 3 –BT–Pd catalysts were found to be highly active in mild hydrodechlorination (HDC) of 2,4-dichlorophenols (DCPs) using formic acid as a hydrogen source. The 2,4-DCPs were completely dechlorinated in 4 h at 30°C and under atmospheric pressure. During the catalytic HDC, the stabilizing capability of BT successfully prevented the leakage and aggregation of Pd NPs, thus ensuring a high cycling stability with stable and high catalytic activity. The Al 2 O 3 –BT–Pd catalysts were recycled six times, without obvious loss of activity. In the sixth cycle, the catalytic HDC yield still reached 98.29% under the same reaction conditions, superior to the control catalysts, including γ-Al 2 O 3 supported Pd NPs (Al 2 O 3 –Pd) and powdered activated carbon supported Pd NPs (AC–Pd). Furthermore, the Al 2 O 3 –BT–Pd also showed high activity in the mild catalytic HDC of 2,4,6-trichlorophenols and chlorobenzene derivatives. Our results demonstrated efficient catalysts to address the environmental issue of chlorophenol pollution.
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CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Feifei Wang,Xiaolin Yu,Maofa Ge,Sujun Wu
A series of TiO 2 and γ-Fe 2 O 3 co-doped graphene oxide (GO) nanosheets ( x TiO 2 /γ-Fe 2 O 3 /GO) were prepared by a facile self-assembly method. The characterization results show that the x TiO 2 /γ-Fe 2 O 3 /GO have the advantages of narrow band gap energies (<2.47 eV), and high structure stability. The incorporation of TiO 2 into γ-Fe 2 O 3 /GO composite dramatically enhances the catalytic activity, and the 0.03TiO 2 /γ-Fe 2 O 3 /GO composite exhibits the highest catalytic efficiency (99%) for ciprofloxacin (CIP) degradation (10 mg/L, 50 ml) within 140 min under visible light, which is ~1.5 times higher than that of γ-Fe 2 O 3 /GO composite without TiO 2 . Furthermore, the photo-Fenton like mechanism was proposed by quenching experiment and electrochemistry method. The intermediates of the CIP degradation were analyzed by the assistance of LC-MS technology, which provides insight into the pathway of CIP degradation.
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