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| 2. |
- Wang, Hao, et al.
(författare)
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Preparation and Properties of Microporous Nickel with High Porosity
- 2023
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Ingår i: Rare Metal Materials and Engineering. - : Northwest Institute for Nonferrous Metal Research. - 1002-185X. ; 52:3, s. 876-882
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Tidskriftsartikel (refereegranskat)abstract
- The strategy of sintered closed-hole followed by reopening was proposed to prepare the microporous nickel material with high porosity through the powder metallurgy and subsequential treatments. The carbonyl nickel powder with particle size of 1 mu m was used as raw material, and the effects of sintering process parameters on the pore properties and mechanical properties of microporous nickel were studied. Results show that the porosity measured by mercury injection method of microporous nickel is 53.7%, and the average pore diameter is 612.25 nm at the sintering temperature of 400 degrees C. After machining, the porosity measured by mercury injection method is 54.0%, and the average pore diameter is 511.37 nm, which still satisfies the requirements of engineering application. The strategy provides providing a new approach for the preparation of microporous nickel and other porous metal materials.
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| 3. |
- Wang, Hongdong, et al.
(författare)
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Superlubricity of Polyalkylene Glycol Aqueous Solutions Enabled by Ultrathin Layered Double Hydroxide Nanosheets
- 2019
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Ingår i: ACS Applied Materials and Interfaces. - : American Chemical Society (ACS). - 1944-8244 .- 1944-8252. ; 11:22, s. 20249-20256
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Tidskriftsartikel (refereegranskat)abstract
- It was previously proved that the existence of a large amount of hydrogen ions in water-based lubricants can easily lead to a superlubric state; however, it was also shown that these hydrogen ions could cause severe corrosion. As part of a large family of attractive clays, layered double hydroxides (LDHs) possess excellent tribological properties in water-based lubrication systems. In the present work, two different kinds of LDHs are dispersed in polyalkylene glycol (PAG) aqueous solutions, in two distinct forms: ultrathin nanosheets (ULDH-NS) of ca. 60 nm wide and ca. 1 nm thick (single or double layer) and nanoparticles (LDH-NP) of ca. 19.73 nm wide and ca. 8.68 nm thick. We find that the addition of ULDH-NS greatly shortens (as much as 85%) the running-in period prior to reaching the superlubricity regime and increases the ultimate load-bearing capacity by about four times. As compared to the fluid film thickness of the lubricating PAG solution, their ultrathin longitudinal dimension will not impair or influence the fluid film coverage in the contact zone. The analysis of sliding solid surfaces and the atomic force microscope microscale friction test demonstrate that the adsorption of ULDH-NS enables the sliding solid surfaces to be polished and protected because of their relatively weak interlayer interaction and increased adhesion effect. Owing to their superior tribological properties as lubricant additives, ultrathin LDH nanosheets hold great potential for enabling liquid superlubricity in industrial applications in the future.
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| 4. |
- Wang, Lei, et al.
(författare)
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Coumarin derivative trigger controlled photo-healing of ion gels and photo-controlled reversible adhesiveness
- 2021
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Ingår i: European Polymer Journal. - : Elsevier. - 0014-3057 .- 1873-1945. ; 144
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Tidskriftsartikel (refereegranskat)abstract
- Fabrication strategies for photo-responsive ion gels have attracted attention owing to their precise spatial and temporal control with predetermined responses to light stimuli. In this work, a reversible light-driven method was introduced to devise photo-responsive ion gels by harnessing coumarin-based building blocks under 365 nm irradiation. A series of random copolymers composed of N, N-dimethylacrylamide (DMA) and 7-(2′-methacryloyloxyethoxy)–4-methylcoumarin (MAOEMC), namely P(DMA-r-MAOEMC), were synthesized through reversible addition-fragmentation chain transfer (RAFT) polymerization with sufficient molecular weight (≈100 kDa). The coumarin moieties in those polymers exhibited a reversible photo-induced dimerization and photocleavage behavior in 1-ethyl-3-methylimidazolium bis (trifluoromethylsufonyl) imide ([C2mim][NTf2]). Those polymers - ionic liquid system at high polymer concentration (20 wt%) under suitable wavelength UV light irradiation led to sol–gel transition, which could be functionalized as photo-healable material and photo-controlled adhesion agents. Notably, the photo-controlled adhesiveness was reversible and can be mediated from 1.2 MPa to 0.2 MPa. This work opens new avenues to develop multifunctional ion gels using dynamic covalent bonds.
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| 5. |
- Wang, Tongfang, et al.
(författare)
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Molecular dynamics study on structural characteristics and mechanical properties of sodium aluminosilicate hydrate with immobilized radioactive Cs and Sr ions
- 2023
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Ingår i: Applied Clay Science. - : Elsevier Ltd. - 0169-1317 .- 1872-9053. ; 243
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Tidskriftsartikel (refereegranskat)abstract
- As a low-carbon, environment-friendly and economical resource for nuclear power generation, radionuclide emission and storage has received worldwide attention. Geopolymer concrete is a green and sustainable building material that can be used to immobilize radionuclides. In the present study, molecular dynamics simulations were conducted to investigate the structural and mechanical properties of sodium aluminosilicate hydrate (NASH) gel, the main component of geopolymer concrete, with/without immobilized radioactive Cs and Sr ions. The three-dimensional structure of NASH gel enabled good immobilization of both radioactive Cs and Sr ions owing to the large radius of Cs ions and high charge density of Sr ions. Addition of Cs ions reduced the strength of the gel and increased the fracture strain, whereas addition of Sr ions increased the strength and significantly increased the ductility. Addition of Sr ions increased the number of penta-coordinated Al in the structure. Consequently, breakage of these bonds required more energy to be absorbed from outside. The nanoscale molecular dynamics simulations provided a theoretical support at atomic level for understanding the structural and mechanical characteristics of geopolymers pertinent to the immobilization of nuclear waste.
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| 6. |
- Zhao, Jun, et al.
(författare)
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Real-Time and Online Lubricating Oil Condition Monitoring Enabled by Triboelectric Nanogenerator
- 2021
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Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 15:7, s. 11869-11879
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Tidskriftsartikel (refereegranskat)abstract
- An intelligent monitoring lubricant is essential for the development of smart machines because unexpected and fatal failures of critical dynamic components in the machines happen every day, threatening the life and health of humans. Inspired by the triboelectric nanogenerators (TENGs) work on water, we present a feasible way to prepare a self-powered triboelectric sensor for real-time monitoring of lubricating oils via the contact electrification process of oil-solid contact (O-S TENG). Typical intruding contaminants in pure base oils can be successfully monitored. The O-S TENG has very good sensitivity, which even can respectively detect at least 1 mg mL-1 debris and 0.01 wt % water contaminants. Furthermore, the real-time monitoring of formulated engine lubricating oil in a real engine oil tank is achieved. Our results show that electron transfer is possible from an oil to solid surface during contact electrification. The electrical output characteristic depends on the screen effect from such as wear debris, deposited carbons, and age-induced organic molecules in oils. Previous work only qualitatively identified that the output ability of liquid can be improved by leaving less liquid adsorbed on the TENG surface, but the adsorption mass and adsorption speed of liquid and its consequences for the output performance were not studied. We quantitatively study the internal relationship between output ability and adsorbing behavior of lubricating oils by quartz crystal microbalance with dissipation (QCM-D) for liquid-solid contact interfaces. This study provides a real-time, online, self-powered strategy for intelligent diagnosis of lubricating oils.
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| 7. |
- Cao, Jie, et al.
(författare)
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Molecular dynamics simulations of ion migration and adsorption on the surfaces of AFm hydrates
- 2023
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Ingår i: Applied Surface Science. - : Elsevier. - 0169-4332 .- 1873-5584. ; 615
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Tidskriftsartikel (refereegranskat)abstract
- Chloride salts can cause severe corrosion damage to reinforcing steel bars in cement-based materials whereas nitrite salts inhibit corrosion. The storage and release of these two anions in cement materials occurs mainly at the interface of monosulfoaluminate (AFm) hydrates. In this paper, molecular dynamics are used to analyze the interaction between anions and AFm phases and clarify the competitive relationships between the anions at adsorption sites on the AFm surface. It was found that the ordered structure of the [Ca2Al(OH)6]+ layers of the AFm plays a key role in anion adsorption and that the mobility of ions desorbed from AFm layers decreases linearly with increasing proximity to the AFm surfaces.
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| 8. |
- Chen, Long, et al.
(författare)
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Pore size dependent molecular adsorption of cationic dye in biomass derived hierarchically porous carbon
- 2017
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Ingår i: Journal of Environmental Management. - : Elsevier. - 0301-4797 .- 1095-8630. ; 196, s. 168-177
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Tidskriftsartikel (refereegranskat)abstract
- Hierarchically porous carbon adsorbents were successfully fabricated from different biomass resources (softwood, hardwood, bamboo and cotton) by a facile two-step process, i.e. carbonization in nitrogen and thermal oxidation in air. Without involving any toxic/corrosive chemicals, large surface area of up to 890 m2/g was achieved, which is comparable to commercial activated carbon. The porous carbons with various surface area and pore size were used as adsorbents to investigate the pore size dependent adsorption phenomenon. Based on the density functional theory, effective (E-SSA) and ineffective surface area (InE-SSA) was calculated considering the geometry of used probing adsorbate. It was demonstrated that the adsorption capacity strongly depends on E-SSA instead of total surface area. Moreover, a regression model was developed to quantify the adsorption capacities contributed from E-SSA and InE-SSA, respectively. The applicability of this model has been verified by satisfactory prediction results on porous carbons prepared in this work as well as commercial activated carbon. Revealing the pore size dependent adsorption behavior in these biomass derived porous carbon adsorbents will help to design more effective materials (either from biomass or other carbon resources) targeting to specific adsorption applications.
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| 9. |
- Ji, Tuo, et al.
(författare)
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Green Processing of Plant Biomass into Mesoporous Carbon as Catalyst Support
- 2016
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Ingår i: Chemical Engineering Journal. - : Elsevier BV. - 1385-8947 .- 1873-3212. ; 295, s. 301-308
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Tidskriftsartikel (refereegranskat)abstract
- Four different plant biomass, bamboo, cotton, soft wood and hard wood, were utilized as carbon precursors to fabricate porous carbon catalyst supports via a chemical free approach. Large surface area with unique mesoporous structure was successfully created in the carbon, which made them suitable for catalyst support. After decorating silver nanoparticles onto these carbon supports, nitroaromatics reduction reactions were performed to evaluate the catalyst activity. Results indicate that chemical composition and surface groups of carbon supports determine the metal catalyst nucleation/growth while the porous microstructure of support affects the mass transport of reactant/product across the liquid/catalyst interface. Among the four selected biomass, porous carbon manufactured from soft wood acquires the highest average pore size, pore volume, mesopore volume fraction and best catalytic activity after decorating silver nanoparticles. This work not only presents an environmental benign process that converts natural biomass into effective porous carbon catalyst supports, but also offers a comprehensive understanding of biomass structure/composition relating to their suitability as catalyst support.
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