CHEMICAL ENGINEERING JOURNAL
·
2017
·
IF 6.216
Wenwu Zhou,Yasong Zhou,Qiang Wei,Sijia Ding,Shujiao Jiang,Qing Zhang,Meifang Liu
Mesoporous Y composites which exhibit both crystallized micropores and large mesopores with narrow mesopore diameter distributions and controlled pore diameters were successfully synthesized. The composite is synthesized through an elaborate design of the SiO 2 @cationic surfactant cetyltrimethylammonium bromide (SiO 2 @CTAB) micelle swelled by an appropriate amount of 1,3,5-trimenthylbenzene (TMB); it is subsequently fabricated from the condensing of the Y zeolite precursors, which contain Y zeolite seeds, on the mesoscale micelle followed by a hydrothermal crystallization process. The effect of synthesis conditions such as the amounts of CTAB, TMB and TEOS added to the synthesis system on the physicochemical properties of the obtained products was examined. The as-synthesized materials were carefully characterized by employing XRD, N 2 adsorption–desorption, SEM, TEM and pyridine-adsorbed FTIR techniques. The mesoporous Y zeolite exhibited both the typical diffraction characteristics of Y zeolites in the wide-angle XRD pattern, and the typical diffraction characteristics of a narrowly dispersed mesopore structure in the small-angle XRD pattern is successfully synthesized for the first time. Finally, the adsorption capacity for DBT and 4,6-DMDBT by samples with different mesopore diameters were assessed by a batch method. Sample MY-0.5C-0.35T-0.9B showed the highest capacity for adsorbing DBT in model diesel, and sample MY-0.5C-0.35T-1.5B showed the highest capacity for adsorbing 4,6-DMDBT in model diesel. Most importantly, sample MY-0.5C-0.35T-1.5B showed the highest adsorptive rate for both DBT and 4,6-DMDBT, which is at least 10 times faster than that of sample MY-0C-0.35T-0B because of the elimination of the diffusion limitation.
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高影响因子
Metals
·
2025
·Vol. 15
·期 3
·307
·
IF 2.5
Ziyang Ruan,Zifan Zhao,Jing Feng
Rare-earth tantalates (RETaO4) are considered as a type of emerging thermal barrier coating materials applied to the hot components of gas turbines and aerospace engines due to their excellent thermal stability, high-temperature fracture toughness, corrosion resistance and extremely low thermal conductivity. However, the relatively low hardness and thermal expansion coefficients may limit their service lifetime in a harsh engine environment. To address the current limitation of rare-earth tantalates and further optimize the mechanical and thermal properties, the defective fluorite-structured Y₂Zr₂O₇ (YZ) was introduced as a second phase into the YTaO4(YT) matrix to form YT1−x–YZx(x = 0, 0.25, 0.5, 0.75, 1) composite ceramics in this work. The mechanical and thermal properties of YT1−x–YZxcomposite ceramics are significantly improved compared to pure-phase YTaO4ceramics. The Vickers hardness of YT1−x–YZx(x = 0.25, 0.5, 0.75) composite ceramics is 9.1~11.3 GPa, which are 2~2.5 times higher than that of YTaO4(4.5 GPa). Among them, YT0.75–YZ0.25exhibits a maximum fracture toughness (3.7 ± 0.5 MPa·m1/2), achieving a 23% improvement compared to YTaO4(3.0 ± 0.23 MPa·m1/2) and a 118% improvement compared to Y2Zr2O7(1.73 ± 0.28 MPa·m1/2). The enhancement is attributed to the combined effect of the intrinsic strengthening of the second phase, as well as the residual stress and grain refinement caused by the introduction of a second phase. Additionally, the thermal expansion coefficients of YT1−x–YZxcomposite ceramics at 1673 K range from 10.3 × 10⁻⁶ K⁻1to 11.0 × 10⁻⁶ K⁻1, which is also higher than that of YTaO4(10.0 × 10−6K−1). Consequently, the superior mechanical and thermal properties indicate that YT–YZ composite ceramics possess promising application prospects for thermal barrier coatings.
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Laser & Photonics Reviews
·
2026
·
IF 9.7
Dawei Wen,Haoyuan Weng,Bin Xiao,Pan Wang,Ruijing Fu,Zhiwei Ma,Qingguang Zeng,Guanjun Xiao
Luminescence pressure sensors, valued for their remote sensing capability and high resolution, have been developed recently. However, most current sensors rely on a linear relationship between an optical property and pressure. We propose a nonlinear machine learning (ML) method to model the luminescence intensity ratio (LIR) as a function of pressure. The versatility and performance of this method are demonstrated using (Y,Gd)(Al,Ga) 3 (BO 3 ) 4 :Cr 3+ phosphors as luminescent pressure sensors. The relative sensitivities of the 2 E → 4 A 2 / 4 T 2 → 4 A 2 LIRs in (Y,Gd)(Al,Ga) 3 (BO 3 ) 4 :Cr 3+ range from 1.58%/GPa to 25.27%/GPa. The ML fitting demonstrates a superior performance compared to linear fitting, with lower mean absolute errors (0.0355–0.1499 GPa vs. 0.1209–0.6955 GPa) and higher R 2 values (99.70–99.98% vs. 93.69–99.79%). The ML fitting method is more suitable for modeling the nonlinear relationships between LIR and pressure than traditional linear fitting. The nonlinear ML fitting approach offers a powerful new way to model the relationships between luminescence features and various physical parameters.
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NEW JOURNAL OF CHEMISTRY
·
2026
·
IF 2.6
Jiming Wang,Min Ji,Min Wang
The integration of photocatalysis and thermal catalysis offers a sustainable route to drive the dry reforming of methane (DRM) at low temperatures, addressing the high energy consumption of traditional thermocatalytic processes. Herein, we systematically explore the effects of doping rare earth elements (Ce, Pr, and Y) on the photothermal catalytic activity and stability of Ni-based catalysts (Ni–MOx–Al2O3) for DRM. Results demonstrate that Ce doping significantly enhances charge carrier separation efficiency and reduces interfacial impedance, endowing Ni–Ce–Al with superior photocatalytic activity compared to Ni–Pr–Al and Ni–Y–Al catalysts. After 100 h of continuous reaction at 650 °C, the conversions of CH4 and CO2 only decrease from 59.0% and 62.0% to 52.6% and 56.8%, respectively. Mechanistic studies reveal that Ce incorporation increases the density of surface oxygen vacancies, which promotes the activation of CH4 and CO2 and enhances coke resistance under light conditions. Kinetic analysis confirms that Ni–Ce–Al possesses the lowest activation energies for CH4 (40.6 kJ mol−1) and CO2 (36.7 kJ mol−1) dissociation under illumination. This work provides helpful guidance for the design of high-performance Ni-based photothermal catalysts for DRM through rare earth modification, highlighting the crucial role of Ce in optimizing electronic properties and anti-coking ability.
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高影响因子
FUEL
·
2022
·
IF 8.035
Jun Liu,Yu Zhang,Zhoujie Liang,Guojie Zhang,Ying Wang,Yuqing Zhao,Guoqiang Li,Yongkang Lv
In this paper, a series of bimetallic catalysts with different Ni/Co ratios were prepared by co-impregnation method for application in methane dry reforming reaction. The effects of different Ni/Co ratios on the catalyst performance were investigated. The catalysts were characterized by XRD, BET, H 2 -TPR, TG, TEM and FTIR. The results showed that after the introduction of a certain amount of Co, the synergistic effect between Ni and Co enhanced the active component-carrier interaction, thus improving the dispersion of the active component of the catalyst, reducing the particle size of the metal, and increasing the activity of the catalyst. Meanwhile, the mechanistic study showed that the introduction of Co species with strong oxygen affinity facilitated the formation of oxygen vacancies. It makes the catalysts contain higher lattice oxygen and carbonate species, which was conducive to the elimination of carbon accumulation, thus improving the stability of catalysts. Therefore, the 10Ni-8Co-10Y/WC-AC catalyst exhibited excellent dry reforming of methane (DRM) performance at a Ni/Co ratio of 5:4. The conversions of CO 2 and CH 4 were 95 % and 88 % at 800 °C under atmospheric pressure, respectively.
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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2022
·
IF 10.319
Liang Xu,Lei Su,Hongjie Wang,Hongfei Gao,Pengfei Guo,Min Niu,Kang Peng,Lei Zhuang,Zhiwei Dai
Materials with ultralow thermal conductivity and good thermal stability are of great interest in numerous applications such as energy storage and conversion devices, and thermal insulation components. In this work, a family of high-entropy Sm 2 B 2 O 7 (B=Ti, Zr, Sn, Hf, Y, Yb, Nb, and Ta) oxides with highly disordered cations on the B-site has been synthesized by introducing large atomic-size mismatch, mass and charge disorder. Through tuning the composition, the high-entropy Sm 2 B 2 O 7 oxides can be engineered from pyrochlore to fluorite structure, accompanied with an order-disorder transition. The pyrochlore Sm 2 (Nb 0.2 Sn 0.2 Ti 0.2 Y 0.2 Zr 0.2 ) 2 O 7 and fluorite Sm 2 (Nb 0.2 Ta 0.2 Y 0.2 Yb 0.2 Zr 0.2 ) 2 O 7 exhibit low thermal conductivities of 1.35 W·m −1 ·K −1 and 1.23 W·m −1 ·K −1 , respectively, indicating their good thermal insulation. In addition, the high-entropy fluorite Sm 2 (Nb 0.2 Ta 0.2 Y 0.2 Yb 0.2 Zr 0.2 ) 2 O 7 also shows average thermal expansion coefficient of 10.2 × 10 −6 °C −1 and high-temperature stability even after thermal exposure at 1600 °C in air for 30 h. These results indicate that the high-entropy Sm 2 B 2 O 7 (B=Ti, Zr, Sn, Hf, Y, Yb, Nb, and Ta) can be promising candidates for thermal barrier coatings and thermally insulators.
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ACS Catalysis
·
2020
·
IF 12.35
Peng Liu,Zhi Li,Xingyu Liu,Weiyu Song,Bowen Peng,Xinyue Zhang,Suofu Nie,Penghui Zeng,Zhongdong Zhang,Xionghou Gao,Baojian Shen
In fluid catalytic cracking (FCC), Brønsted acid plays a very important role. Herein, a zinc-modified ultrastable Y (USY) zeolite containing higher Brønsted acidity was prepared by synergistic treatment with zinc chloride and steaming. The results of characterization showed that selective dealumination and silicon healing due to introduction of zinc ions ([ZnCl]+ and [ZnOH]+) into zeolite could promote the formation of extra-framework silicon (EFS) and different silicon healing of the Al vacancies, which led to the formation of half-sodalite cages connecting with supercages and thus increased the availability of acidic sites in the sodalite cage. Meanwhile, DFT calculations demonstrated that the acidic strength of protons in the sodalite cage was enhanced by [ZnCl]+ and [ZnOH]+, and the synergy of Brønsted/[ZnCl]+ became stronger. As a result, the strong Brønsted acid was increased by 19%. This translated to higher n-octane and heavy oil (VGO) catalytic cracking activity and gasoline yield.
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高影响因子
RARE METALS
·
2021
·Vol. 41
·期 2
·650-662
·
IF 4.003
Guo Hua,Li Jun,Zou Xian-Rui,Wang Hong-Shui,Kang An,Zhou Huan,Li Ming-Jun,Zhao Xiao-Yan
Abstract Development of photocatalytic materials able to profit from the whole spectrum of sun for efficient organic pollution removal and bacterial elimination is a fascinating strategy in environmental engineering. In current work, GO-TiO 2 /(Ca,Y)F 2 :Tm,Yb, a full-spectrum composite photocatalyst, was prepared via hydrothermal processing with TiO 2 /(Ca,Y)F 2 :Tm,Yb particles deposited on the surface of graphene oxide (GO). The surface properties of GO-TiO 2 /(Ca,Y)F 2 :Tm,Yb were characterized using various characterization techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and Brunauer–Emmett–Teller (BET) surface area analyzer. Besides, ultraviolet–visible (UV–Vis) diffuse reflectance spectroscopy, electron spin resonance (ESR) and other methods were used to systematically explore the photocatalytic mechanism of GO enhancement of TiO 2 /(Ca,Y)F 2 :Tm,Yb. In photocatalytic degradation study, the degradation rate of methyl orange (MO) was improved by 40% when GO was added into the TiO 2 /(Ca,Y)F 2 :Tm,Yb system. In addition, the presence of GO also improves the antibacterial ability of TiO 2 /(Ca,Y)F 2 :Tm,Yb against Escherichia coli and Staphylococcus aureus . All results reveal high efficacy of GO-TiO 2 /(Ca,Y)F 2 :Tm,Yb under full spectrum light irradiation, in which (Ca,Y)F 2 :Tm,Yb and TiO 2 can improve its utilization of full spectrum sunlight, and GO can enhance adsorption ability of dye and electron–hole pair differentiation ability of TiO 2 /(Ca,Y)F 2 :Tm,Yb. Graphic abstract
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2021
·
IF 5.816
Wenjie Yang,Chao Han,Yuehua Li,Huizhu Zhou,Shan Liu,Ling Wang,Zhangxing He,Lei Dai
BaHf 0.8 Ln 0.2 O 3-δ doped with rare earth elements with different ionic radii (Ln = Yb , Y, Dy and Gd) as candidate materials for solid oxide fuel cells and H 2 separation membrane have been prepared. Their phase composition , sinterability , chemical stability and conductivity were studied systematically. The rare earth elements are successfully incorporated into the main phase crystal lattice of barium hafnate to generate a single perovskite phase. The relative density of all samples sintered at 1600 °C reaches above 90%, and Y-doped BaHfO 3 has the highest relative density (94.7%) and the biggest grain size (about 1 μm) among all samples. The conductivities of the samples firstly increase and then decrease with the increase of the doped ion radius. Among all samples the conductivity of BaHf 0.8 Y 0.2 O 3-δ is the highest and reaches 6.02 × 10 −3 S cm −1 in wet air at 700 °C, which is attributed to the good sinterability and suitable crystal structure (tolerance factor and free volume). All samples also show excellent chemical stability in the test atmospheres, including saturated H 2 O steam, pure H 2 and CO 2 , 200 ppm H 2 S/Ar and boiling water. The Pt/BaHf 0.8 Y 0.2 O 3-δ electrolyte/Pt single cell was fabricated with a 530 μm-thick disk and its electrochemical properties were tested. The peak power density reaches 10.21 mW cm −2 at 700 °C, which is comparable to similar fuel cells reported. These results suggest that BaHf 0.8 Y 0.2 O 3-δ is a promising electrolyte candidate for proton-conducting fuel cells.
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Materials Science & Engineering C-Materials for Biological Applications
·
2017
·
IF 4.164
Peizong Deng,Fangfang Teng,Feilong Zhou,Zhimei Song,Ning Meng,Na Liu,Runliang Feng
Ketoconazole is a hydrophobic broad-spectrum antifungal agent for skin infection therapy. In order to develop topical formulation of ketoconazole for improving its selective skin deposition and water-solubility, ketoconazole-loaded Y-shaped monomethoxy poly(ethylene glycol)-block-poly(ɛ-caprolactone) micelles were prepared through thin-film hydration method with high entrapment efficiency (96.1 ± 0.76%) and small particle (about 58.66 nm). The drug-loaded micelles showed comparative in vitro antimicrobial activity with KET cream. In e x in vivo skin deposition and permeation study, ketoconazole-loaded micelles provided skin accumulation higher than marketed ketoconazole cream without obvious permeation in the whole period. Fluorescence microscopy study and histopathological study demonstrated the copolymeric micelles' penetrating into skin in depth due to its capability of weakening the barrier function of stratum corneum. In vivo skin deposition parameters further confirmed high skin deposition of drug-loaded micelles (AUC (0-t) = 396.16 μg·h/cm 2 ) over marketed ketoconazole cream (AUC (0-t) = 250.03 μg·h/cm 2 ). Meanwhile, in vivo pharmacokinetic parameters proved that ketoconazole-loaded micelles reduced ketoconazole's distribution in blood in comparison with the cream (AUC (0-t) = 93,028.00 μg·h/L vs AUC (0-t) = 151,714.00 μg·h/L), meaning lower possibility of its systemic unwanted effects in the skin fungal infection treatment. The results suggested that the copolymeric micelles can be adopted for specific delivering ketoconazole into skin for fungal infection cure.
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PubMed
高影响因子
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2016
·Vol. 408
·期 19
·5247-5259
·
IF 3.125
Pan Ziyu,Peng Jingdong,Zang Xu,Lei Gang,He Yan,Liu Di
A novel, highly selective, and sensitive resonance light scattering (RLS) detection approach coupled with high performance liquid chromatography (HPLC) was researched and developed for the synchronous analysis of three kinds of benzimidazole anthelmintics, including mebendazole (MBZ), albendazole (ABZ), and fenbendazole (FBZ) for the first time. In the pH range of 3.5–3.7 Britton-Robinson buffer medium, three kinds of anthelmintics, which were separated by HPLC, reacted with eosin Y (EY) to form 1:1 ion-association complexes, resulting in significantly enhanced RLS signals and the maximum peak located at 335 nm. The enhanced RLS intensity was in proportion to the MBZ, ABZ, and FBZ concentration in the range 0.2–25, 0.2–23, and 0.15–20 μg/mL, respectively. The limit of detection was in the range of 0.064–0.16 μg/mL. In addition, human urine was determined to validate the proposed method by spiked samples and real urine samples. Satisfactory results were obtained by HPLC-RLS method.
The diagram mechanism of generating resonance between emitted light and scattered light
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PubMed
高影响因子
FUEL
·
2024
·
IF 6.7
Zi-Chun Fan,Zhuang Li,Xiang Bai,Xian-Yong Wei,Yierxiati Dilixiati,Qian-Qian Kong,Ji Zhao,Yong-Hui Feng,Zhi-Min Zong,Jun-Long Wang
The catalytic hydroconversion (CHC) of benzyloxybenzene (BOB) and oxydibenzene (ODB), two typical lignite-related model compounds (LRMCs) representing α-Ο-4 and 4-O-5 model linkages , have been investigated using uniformly dispersed Ni 15 /HY prepared by a three-step method. The cleavage of >CH-O- bridged bonds in BOB and partial hydrogenation of ODB are considered as a crucial first step, and the target reactions in this work are to produce complete hydrodeoxidized ring saturation products. Through the exploration of reaction mechanism, H + /H - and biatomic active hydrogen, as the main hydrogen species involved in the reaction, play an important role in the CHC of BOB and ODB. Herein, the synergic effect between the hydrogenation of nickel nanoparticles and the acidic function of Y -type zeolite improves the CHC performance, resulting in Ni 15 /HY displaying proficient catalytic activity and selectivity for the CHC of BOB and ODB. Under the optimal reaction conditions, BOB and ODB can be completely converted to cyclanes over Ni 15 /HY, and the main products are dicyclohexylmethane (57.6 %) and cyclohexane (92.4 %), respectively. The developed Ni 15 /HY can not only promote the hydroconversion of BOB and ODB to produce ring-saturated products, but also undergo the rearrangement reaction to produce two- or three-ring cyclanes, which is desirable to upgrade LRMCs to high-density hydrocarbon fuels .
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