APPLIED SURFACE SCIENCE
·
2024
·
IF 6.3
Yunze Li,Changfeng lu,Kai Gao,Yi Zhang,Lin Zhang,Guoxin Xie
Perfluoropolyether (PFPE) is an excellent high-temperature lubricant; however, its poor affinity with additives such as MoS 2 , a common high-temperature lubricant additive, often leads to agglomeration and settling during storage, thereby reducing its tribological performance. To address this challenge, this study investigates the chemical grafting of MoS 2 using Trimethoxy (1H,1H,2H,2H-perfluorodecyl) silane (TMFS), achieving stable MoS 2 dispersion in PFPE that remains effective for up to 180 days. The grafted MoS 2 exhibits remarkable thermal stability, maintaining its integrity without decomposition even at temperatures reaching 250 °C. Compared with pure PFPE, the modified lubricant demonstrates a remarkably 36.8 % reduction in coefficient of friction and an 81.6 % decrease in wear rate at 200 °C. This research provides crucial theoretical insights and practical guidance for the future design of high-performance high-temperature lubrication systems.
研究领域:
材料科学
·
化学工程
·
机械工程
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2025
·
IF 8.3
Aihua Yan,Tongyang Zhang,Fei Huang,Quande Wang,Shijian Lu,Wenxue Zhao,Ye Gao,Zigao Su,Huaqi Yuan
Multiplex modification is considered as one of attractive methods to achieve highly-efficient photocatalytic water splitting into hydrogen evolution performance. Herein, MoS 2 /S v -ZnIn 2 S 4 /ZnS (MS/S v -ZIS/ZS) composites were constructed by a facile in-situ engineering technique. The sulfur vacancy, Ohmic-type contact and I-type heterojunction were systematically integrated into the composites. The unique structure could not only facilitate a directional charge transfer and accelerate the charge extraction, but also enhance the charge utilization and improve the hydrogen reduction reaction dynamics. As a result, the composites exhibited a promoted hydrogen evolution rate of 9.5 mmol g −1 h −1 , which was about 3.8 times higher than that of pure ZIS. This work may extend the in-situ preparation strategy and motivate the intensive investigation of high-efficiency ZIS-based photocatalysts.
研究领域:
材料科学
·
能源科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2023
·
IF 13.6
Haoran Yu,Changmin Liu,Shuo Liu,Yu Gu,Shuya Wang,Ali Yaraş,Linchao Hu,Wenyi Zhang,Mingguo Peng,Hasan Arslanoğlu,Linqiang Mao
Spent petroleum refining catalyst is regarded as the important secondary resource for valuable metals. However, common recycling strategies, including soda roasting, acid and alkaline solutions leaching and chemically precipitation, produced large quantities of high salinity wastewater. This study proposed an efficient method to recovery of Mo and Ni from the spent hydrodesulfurization (HDS) catalyst via O 2 -rich roasting and organic acid leaching with the advantage of less salinity wastewater production. The transformation of Mo(IV) into soluble Mo(VI) was enhanced by O 2 -rich atmosphere roasting, and 98.64% of Mo(IV) was oxidized at 650 ℃ for 2 h in atmosphere containing 30% of O 2 . The oxidation process of Mo(IV) was agreed with the shrinkage pore model, and regulated by surface reaction and internal diffusion. 97.97% of Mo(VI) was leached from roasted product by oxalic acid , separated with complexation extraction agent of Ala-TBP and recovered as (NH 4 ) 8 Mo 10 O 34 and (NH 4 ) 2 Mo 3 O 10 by evaporative crystallization. Ni was leached out from spent catalyst with 1 mol/L acetic acid, and precipitated as NiC 2 O 4 with oxalic acid . 95.92% of Mo and 96.77% of Ni were recovered from spent HDS catalyst with this recycling route. This study provided a high-efficient and eco-friendly method to recovery of valuable metals from spent catalyst.
研究领域:
环境科学
·
冶金工程
✓ 已验证
DOI
PubMed
高影响因子
Sustainability
·
2024
·Vol. 16
·期 5
·1945
·
IF 3.3
Zhongming Wu,Jianxin Deng,Tuanwei Zhao,Yang Zhou,Yongfu Kang,Xiangxiang Bai,Fei Hong,Longfei Fu,Gensheng Li,Zhiyi Zhang,Weiming Guan
Rapid economic development and increased demand for mineral products in China have led to extensive extraction of various ores, resulting in significant environmental challenges associated with the generation of industrial solid waste, particularly iron tailings. Despite being a major mining nation, China faces issues of wasteful practices, with substantial amounts of valuable elements lost during the processing of iron ore. This study addresses the urgent need for sustainable solutions by proposing an innovative approach for the recovery of valuable elements from iron tailings. The proposed process involves a sequential application of acid leaching, chemical precipitation, and Metal-Organic Frameworks (MOFs) ion adsorption. The pre-treated iron tailings were leached in HCl solution with pH 1.5 at 70 °C for 2 h, and the co-leaching efficiency of 98.1% V, 98.2% Mo, 99.3% Fe, and 98.7% Mg was obtained. Chemical precipitation is then employed to isolate Fe, Mg V, and Mo and promote the formation of targeted compounds, ensuring concentration and purity. The integration of MOF ion adsorption, known for its high surface area and tunable pore structures, provides an efficient platform for selectively capturing and recovering target ions. 97.7% V and 96.3% Mo were selectively extracted from Zirconium 1,4-carboxybenzene metal-organic framework (UiO-66) adsorption system with pH 5.0 at 30 °C for 6 h, and 91.7% V and 90.3% Mo were selectively extracted from 2-methylimidazole zinc salt metal-organic framework (ZIF-8) adsorption system with pH 5 at 30 °C for 6.0 h. This three-stage process offers an efficient method for the recovery of valuable elements from iron tailings.
研究领域:
环境科学
·
冶金工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2024
·
IF 9.4
Jiuli Chang,Fengfeng Song,Yan Hou,Dapeng Wu,Fang Xu,Kai Jiang,Zhiyong Gao
H 2 and formate are important energy carriers in fuel-cells and feedstocks in chemical industry. The hydrogen evolution reaction (HER) coupling with electro-oxidative cleavage of thermodynamically favorable polyols is a promising way to coproduce H 2 and formate via electrochemical means, highly active catalysts for HER and electrooxidative cleavage of polycols are the key to achieve such a goal. Herein, molybdenum (Mo), tungsten (W) doped cobalt phosphides (Co 2 P) deposited onto nickel foam (NF) substrate, denoted as Mo-Co 2 P/NF and W-Co 2 P/NF, respectively, were investigated as catalytic electrodes for HER and electrochemical glycerol oxidation reaction (GOR) to yield H 2 and formate. The W-Co 2 P/NF electrode exhibited low overpotential ( η ) of 113 mV to attain a current density ( J ) of −100 mA cm −2 for HER, while the Mo-Co 2 P/NF electrode demonstrated high GOR efficiency for selective production of formate. In situ Raman and infrared spectroscopic characterizations revealed that the evolved CoO 2 from Co 2 P is the genuine catalytic sites for GOR. The asymmetric electrolyzer based on W-Co 2 P/NF cathode and Mo-Co 2 P/NF anode delivered a J = 100 mA cm −2 at 1.8 V voltage for glycerol electrolysis, which led to 18.2 % reduced electricity consumption relative to water electrolysis. This work highlights the potential of heteroelement doped phosphide in catalytic performances for HER and GOR, and opens up new avenue to coproduce more widespread commodity chemicals via gentle and sustainable electrocatalytic means.
研究领域:
材料科学
·
电化学
·
催化反应
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Zechao Huangfu,Wei Sun,Runqing Liu,Chen Chen,Chenyang Zhang,Heng Yu,Siyuan Liu
The effective recovery of talc-bearing molybdenum ores has been a research hotspot in the field of minerals processing, which is mainly attributed to the similarity of the physical and chemical properties of talc and molybdenite, especially floatability, which presents a challenge in the separation of the two during the beneficiation process. Herein, the coordination affinity, differentiated adsorption configurations, adsorption morphology, and bonding mechanisms of a polysaccharide-based depressant, carboxymethyl starch (CMS), on the layered hydrophobic minerals molybdenite and talc have been compared and its special use in flotation was investigated by various advanced techniques, including density functional theory (DFT) simulation, time-of-flight secondary ion mass spectrometry (TOF-SIMS) and X-ray photoelectron spectroscopy (XPS). The CMS adsorption on the talc surface was more affinitive than that of molybdenite and it is possible to achieve the selective separation of laminar hydrophobic minerals molybdenite and talc through the utilization of differential wettability. Flotation kinetics with 400 mg/L CMS as a depressant and 3*10 −3 mol/L sodium diethyldithiocarbamate (DDTC) as a collector has highlighted the importance of the mineral particle sizes that the better depressant activity of CMS on the coarse-grained talc surface in comparison to that of molybdenite is attributed to the greater adsorption energy and more homogeneous adsorption morphology of CMS on the talc basal surface which is the dominant surface affecting the floatability.
研究领域:
矿物加工工程
·
材料科学与工程
✓ 已验证
产品关联
DOI
高影响因子
ENVIRONMENTAL POLLUTION
·
2022
·
IF 9.988
Lu Jiang,Pingxiao Wu,Yijing Xu,Yihao Li,Meiqing Chen,Zubair Ahmed,Nengwu Zhu
Triclinic birnessite (TB), a typical layered Mn oxide which is abundant naturally occurring minerals with a vital impact on the transformation of arsenite (As(III)) by adsorption and oxidation . As one of the most common critical metalloids , ammonium ion (NH 4 + ) universally coexists with birnessite in marine, sediments or groundwater where are contaminated with As(III). In this study, we investigated the impacts of NH 4 + on TB towards the transformation of As(III). Compared with the original TB (40.1%), the As(III) removal efficiencies of three different concentration (0.5 M, 1 M and 2 M) NH 4 + impressed triclinic birnessite (TB-0.5 N, TB-1N and TB-2N) are increased rapidly in the order of: TB-2N (80.4%) > TB-1N (75.8%) > TB-0.5 N (71.5%). In addition, TB-2N exhibited the highest initial oxidation rate of 0.0031 min −1 which exceeds twice as much as this of TB (0.0014 min −1 ). And TB-2N could reach the max oxidation efficiency when the As concentration is 0.08 mM. Due to two different mechanisms of As(III) oxidation on birnessites under acidic and alkaline conditions, TB-2N showed a higher removal efficiency than TB at pH 3.0, 5.0, 7.0 and 9.0. Hence, there are two main reasons for the advanced As(III) oxidation capacity of TB-2N. One is the improvement of the average oxidation state of Mn, the other is the increase of oxygen vacancy with the coexistence of NH 4 + . Moreover, the larger specific surface area of TB-2N also contribute to enhancing As(III) oxidation capacity. This study holds a fundamental understanding of the behavior of triclinic birnessite which is coexisted with ammonium ion towards the transformation of As(III) in the environment.
研究领域:
环境科学
·
矿物学
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING SCIENCE
·
2025
·
IF 4.3
Tophet Wongladprom,Qi Li,Tianyu Guo,Hui Wu,Jie Li,Gang Wang,Chunshan Li
A highly effective catalyst is desired for CO 2 selective hydrogenation to methanol due to the kinetic limitation of this process, considering the heavy impact of CO 2 emission on global environment. Herein, a type of ammonization-treated CuMo catalyst was developed for CO 2 -to-methanol hydrogenation, which contains MoN and Mo 2 N species. The effect of catalyst preparation conditions on the physicochemical properties of the resulting sample was systematically investigated using multiple characterization techniques, including physical N 2 adsorption and desorption isotherms, XRD, HRTEM, XPS, Cu Auger spectra, H 2 -TPR and CO 2 -TPD. Structure-activity relationships analysis revealed that the proportion of Cu 0 and Mo δ+ (1 < δ < 4) in the catalyst is linearly correlated to the CO 2 transformative rate and methanol selectivity, respectively, which is considered to show synergistic effect on methanol production. Consequentially, the methanol production could reach up to 177.2 mg/g cat /h with a selectivity of 95.7 % at 230 °C and 4 MPa. In addition, the catalytic mechanism exploration employing in situ IR indicated the CO 2 hydrogenation towards methanol follows the formate route, and the Mo δ+ species facilitated the stabilization of CO 2 -derived reactive intermediates on the catalyst surface. Additionally, kinetic studies reveal methanol formation is primarily limited by CO 2 adsorption/activation rather than H 2 dissociation.
研究领域:
催化化学
·
能源化学
·
环境化学
·
材料化学
·
工业催化
·
表面科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2017
·
IF 3.582
Lei Li,Wei Chu,Cheng Ding,Xinguo Xi,Ruiyu Jiang,Jinlong Yan
s Mo-based nanoparticles (MoO 2 and Mo 2 C) embedded in porous carbon matrix have been synthesized by a successive hydrothermal and thermal treatment strategy. The synthesized materials were tested for CO x -free H 2 production via ammonia decomposition . Various characterizations, including N 2 -sorption, TGA , FTIR, TEM, XRD , EDX and XPS, were employed to investigate the morphology, component and structure of fresh and used catalysts. In terms of fresh Mo@C sample, tiny Mo-based nanoparticles (3–6 nm) are homogeneously dispersed in porous carbon matrixes, which were rapidly nitridized to MoN phases during reaction process. Most of MoN species were still embedded in carbon matrixes after 25 h stability test. For comparison, MoN@C sample was achieved via temperature-programmed ammonolysis of Mo@C sample, demonstrating the formation of MoN species and enhanced activities. The ammonia decomposition activity (∼90% conversion) is obtained over MoN@C catalyst at 600 °C and 15,000 h −1 , which is higher than that of non-pretreated Mo@C catalyst. This embedded structure also endows them with a relatively stable performance even at high temperature.
研究领域:
材料科学
·
催化化学
·
纳米技术
·
能源化学
·
氢能存储与利用
✓ 已验证
DOI
高影响因子
Advanced Electronic Materials
·
2018
·Vol. 5
·期 1
·1800548
·
IF 5.466
Changzeng Yan,Tianhang Yu,Chao Ji,Dae Joon Kang,Ning Wang,Rong Sun,Ching-Ping Wong
Ever-increasing packaging and power densities of modern electronic devices in the present “More-than-Moore” technology era demand higher performance thermal interface materials (TIMs). However, conventional composite TIMs require higher loading to achieve better thermal conductive property, resulting in a mechanical problem. The poor wetting property of matrix loading materials further increases the interfacial thermal resistance (ITR). In this work, a one-step hydrothermal method is employed to grow 2D molybdenum disulfide (MoS 2 ) nanosheets on a tellurium (Te) nanowire skeleton and silver (Ag) nanoparticles are further decorated on MoS 2 nanosheets via the photoreduction method. The in-plane thermal conductivity of the final nanocomposite reaches as high as 10.4 W m −1 K −1 , which is 4,160% higher than that of a pure epoxy resin and one order of magnitude higher than that of conventional polymeric nanocomposites. The 3D interconnected heat transferring network of Te/MoS 2 /Ag greatly enhances the thermal stability of the composite in practical applications. The rational materials design concept may contribute to the development of new types of high-performance thermal management materials.
研究领域:
材料科学
·
热管理技术
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2021
·
IF 5.316
Jin Chen,Chun-Li Hu,Yi-Lin Li,Qian-Qian Chen,Bing-Xuan Li,Jiang-Gao Mao
Herein, we reported two alkali metal molybdenum(VI) iodates, namely, NaMoO 3 (IO 3 ) and γ-KMoO 3 (IO 3 ) with 1D and 3D [MoO 3 (IO 3 )] − anionic architectures, respectively. The novel 1D chain in NaMoO 3 (IO 3 ) and the 3D network in γ-KMoO 3 (IO 3 ) are constructed by the 0D Λ-shaped cis -[MoO 4 (IO 3 ) 2 ] 4− building units interconnected by bridging IO 3 − anions as well as the corner-sharing of oxo anions. Importantly, the polar γ-KMoO 3 (IO 3 ) exhibits a very large second-harmonic generation (SHG) effect of 12 × KH 2 PO 4 (KDP) under 1064 nm laser radiation, a high laser-Induced damage threshold value (52 × AgGaS 2 ), and a moderate birefringence of 0.087@1064 nm, whereas the centrosymmetric NaMoO 3 (IO 3 ) has a large birefringence of 0.208@1064 nm. This study further proves the useful route of exploring promising optical materials via assembling the 0D basic building units into higher dimensional anionic architectures.
研究领域:
无机化学
·
材料科学
·
光学
✓ 已验证
DOI
高影响因子
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2025
·
IF 8.5
Junzheng Chen,Xikun Zhang,Xue Lv,Shurui Yi,Di Fang
In this study, the dispersion behavior of MoS₂ in ionic liquids (ILs) with varying alkyl chain lengths was the primary focus of investigation, followed by the design of a novel PAM/SMA/CMC/PDA@MoS 2 hydrogel. By optimizing the concentrations of CMC and PDA@MoS 2 , a bifunctional hydrogel with both sensing and catalytic functions was successfully developed. Mechanical tests revealed that the PAM/SMA/CMC 0.06 /0.09PDA@MoS 2 hydrogel exhibited exceptional mechanical properties, with stress (505.24 kPa), strain (2333.34 %), elastic modulus (20.17 kPa), and toughness (3990.97 kJ/m 3 ). Furthermore, the hydrogel demonstrated superior sensing performance, characterized by high sensitivity (GF = 7.67) and a rapid response time (148 ms) across a wide strain range. These properties enable precise monitoring of physiological movements, coupled with long-term cyclic stability, positioning it as a versatile material for sensors and electrodes. Subsequently, in situ stabilized silver nanoparticles (Ag NPs) were used as a template for the catalytic degradation of methylene blue (MB) using discarded human motion monitoring hydrogels. The degradation followed first-order kinetics (k = 0.54 min −1 at 25 °C) with 85 % efficiency sustained over 10 cycles, demonstrating significant stability and recyclability. This strategy integrates sensor recycling with Ag NPs based dye degradation, addressing environmental concerns and highlighting its potential in sustainable applications.
研究领域:
材料科学
·
环境科学
·
生物医学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）