Publications by authors named "Xianfeng Pei"

Article Synopsis
  • Rubber concrete is studied for its durability in fatigue-resistant structures, focusing on a five-phase material model that includes various components such as rubber and the rubber-mortar interfacial transition zone (ITZ).
  • The ITZ, being a weak area in cement-based materials, significantly affects the mechanical properties and durability of concrete but is challenging to evaluate through standard experiments.
  • The study employs Monofactor analysis and the Plackett-Burman test to identify influencing parameters of the ITZ and uses numerical simulations to optimize these parameters, resulting in improved alignment of simulation data with experimental results, which applies to rubber concrete with varying rubber content.
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The incorporation of rubber can enhance concrete's durability and effectively reduce the damage caused by freeze-thaw cycling (FTC). Still, there has been only limited research on the damage mechanism of RC at the fine view level. To gain insight into the expansion process of uniaxial compression damage cracks in rubber concrete (RC) and summarize the internal temperature field distribution law during FTC, a fine RC thermodynamic model containing mortar, aggregate, rubber, water, and interfacial transition zone (ITZ) is established in this paper, and the cohesive element is selected for the ITZ part.

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Rubber concrete (RC) exhibits high durability due to the rubber admixture. It is widely used in a large number of fatigue-resistant structures. Mesoscale studies are used to study the composition of polymers, but there is no method for fatigue simulation of RC.

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Nuclear factor-erythroid 2 related factor 2 (Nrf2) plays critical roles in attenuating various inflammation- and oxidative stress-induced diseases, including acute lung injury (ALI). Bardoxolone (Bard), a synthetic triterpenoid based on natural product oleanolic acid, is one of the most potent Nrf2 activator. However, if Bard could prevent lipopolysaccharide (LPS)-induced ALI by inducing Nrf2 activation and its down-streaming signals, is still poorly understood.

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Graphene oxide was tailored into GO nanosheets with periodic acid treatment. Interestingly, the latter have a superior sensing performance for the fast and reversible detection of SO(2) compared with the former at room temperature. Its sensing mechanism was proposed from the structural changes of the GO nanosheets during the sensing and recovering processes.

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A novel strategy for the one-pot fabrication of free-standing polypyrrole films is presented in this work. The films are spontaneously formed at an air/ionic liquid interface through interface oxypolymerization. The thicknesses of the films are finely controlled from tens to hundreds of nanometers, and the films are uniform and compact.

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A chiral cationic gelator derived from L-alanine was synthesized. Sol-gel transcriptions were carried out to control mesoporous silica nanostructures using the organic self-assemblies of this gelator as templates. It was found that the morphologies of the obtained mesoporous silicas were sensitive to stirring time.

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A chiral low-molecular-weight amphiphile, L- 18Ala11PyPF(6), was synthesized from L-alanine. Hollow silica nanoworms with circular pore channels parallel to the shell surfaces and holes at the terminals were prepared using the self-assemblies of it as templates via a single-templating approach. The formation of this hierarchical structure was studied by taking TEM images after different reaction time and changing reaction conditions.

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Branched left-handed twisted mesoporous silica nanoribbons were prepared via a template method.

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A new chiral cationic amphiphile has been synthesized. Sol-gel transcriptions were carried out to control mesoporous silica nanostructures using the organic self-assemblies of this amphiphile as templates. Left-handed coiled mesoporous silica nanoribbons were obtained in the mixture of 1-propanol and 2.

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Three chiral cationic gelators were synthesized. They can form translucent hydrogels in pure water. These hydrogels become highly viscous liquids under strong stirring.

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