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Träfflista för sökning "WFRF:(Wu Xiaoli) "

Sökning: WFRF:(Wu Xiaoli)

  • Resultat 1-10 av 12
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1.
  • Chen, Quan, et al. (författare)
  • Influence of CaO on the thermal kinetics and formation mechanism of high value-added products during waste tire pyrolysis
  • 2022
  • Ingår i: Journal of Hazardous Materials. - : Elsevier. - 0304-3894 .- 1873-3336. ; 436
  • Tidskriftsartikel (refereegranskat)abstract
    • There is a lack of detailed research on the production of isoprene and D-limonene by solid base-catalysed thermal depolymerization of waste tires (WTs). This work aimed to investigate the thermal decomposition characteristics, reaction kinetics, high value-added products production and potential mechanisms during WT pyrolysis in the presence of calcium oxide (CaO) via Thermogravimetry-Fourier Transform Infrared spectrometer (TG-FTIR) and Pyrolyzer-Gas Chromatography/Mass spectrometry (Py-GC/MS). The results obtained from TG indicated that CaO accelerated depolymerization in terms of reducing the reaction temperature, which is also reflected in the kinetic parameters. It can be found that the content of D-limonene increased by 13.76% and that of isoprene increased by 37.57%, which were attributed to differences in the depolymerization mechanisms in the presence of CaO. Furthermore, CaO had a profound impact on desulfurization by reducing benzothiazole, sulfoacid, and thiophene. The potential catalytic mechanisms of isoprene and D-limonene production and desulfurization were also proposed. This work deepens the understanding of the catalytic pyrolysis of WT under CaO and unambiguously demonstrates the great potential of CaO in enhancing isoprene and D-limonene production, providing new insight for the cleaner production of high value-added products from WT.
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3.
  • Ding, Hao, et al. (författare)
  • A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling.
  • 2004
  • Ingår i: Nat Genet. - 1061-4036. ; 36:10, s. 1111-6
  • Tidskriftsartikel (refereegranskat)abstract
    • PDGF-C is a member of the platelet-derived growth factor (PDGF) family, which signals through PDGF receptor (PDGFR) alphaalpha and alphabeta dimers. Here we show that Pdgfc(-/-) mice die in the perinatal period owing to feeding and respiratory difficulties associated with a complete cleft of the secondary palate. This phenotype was less severe than that of Pdgfra(-/-) embryos. Pdgfc(-/-) Pdgfa(-/-) embryos developed a cleft face, subepidermal blistering, deficiency of renal cortex mesenchyme, spina bifida and skeletal and vascular defects. Complete loss of function of both ligands, therefore, phenocopied the loss of PDGFR-alpha function, suggesting that both PDGF-A and PDGF-C signal through PDGFR-alpha to regulate the development of craniofacial structures, the neural tube and mesodermal organs. Our results also show that PDGF-C signaling is a new pathway in palatogenesis, different from, and independent of, those previously implicated.
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4.
  • Feng, Zhaoxuan, et al. (författare)
  • Nano graphene oxide creates a fully biobased 3D-printed membrane with high-flux and anti-fouling oil/water separation performance
  • 2024
  • Ingår i: Chemical Engineering Journal. - : Elsevier B.V.. - 1385-8947 .- 1873-3212. ; 485
  • Tidskriftsartikel (refereegranskat)abstract
    • Facile fabrication of green and renewable bio-based membranes with good anti-fouling and oil/water separation performance is of great importance to solve the oil spills and industrial oily wastewater threatening the ecological environment. Here, a fully biobased oil/water separation membrane with an ordered porous structure was 3D printed ultraviolet-assisted direct ink writing. The components of the bio-ink were obtained by methacrylation of chitosan (CS) and gelatin (GEL) to synthesize methacrylated chitosan (CSMA) and methacrylated gelatin (GELMA), while the nanographene oxide (nGO) was derived from CS through a simple microwave-assisted hydrothermal carbonization followed by oxidation step. The addition of nGO boosted the printability of the bio-ink, and the anti-fouling property and water permeation flux of the printed membranes. As a result, the membrane M−CSMA/GELMA/nGO-0.7 with the optimal performance possessed a low water contact angle in air of 0°, and high underwater oil contact angle of 161.5°, demonstrating a combination of superhydrophilic and underwater superoleophobic properties. M−CSMA/GELMA/nGO-0.7 has good corrosion resistance and long service life as evidenced from the separation efficiency of n-heptane/water, which kept above 99.5 % and a high water permeation flux above 38,300 L m−2h−1 after 20 cyclic tests in the harsh aquatic conditions containing 1 M NaCl, 1 M HCl, or 1 M NaOH, respectively. This shows promising potential for real-life applications.
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5.
  • Huang, Wei, et al. (författare)
  • Variation in chemical composition and volatility of oxygenated organic aerosol in different rural, urban, and mountain environments
  • 2024
  • Ingår i: Atmospheric Chemistry and Physics. - 1680-7316 .- 1680-7324. ; 24:4, s. 2607-2624
  • Tidskriftsartikel (refereegranskat)abstract
    • The apparent volatility of atmospheric organic aerosol (OA) particles is determined by their chemical composition and environmental conditions (e.g., ambient temperature). A quantitative, experimental assessment of volatility and the respective importance of these two factors remains challenging, especially in ambient measurements. We present molecular composition and volatility of oxygenated OA (OOA) particles in different rural, urban, and mountain environments (including Chacaltaya, Bolivia; Alabama, US; Hyytiälä, Finland; Stuttgart and Karlsruhe, Germany; and Delhi, India) based on deployments of a filter inlet for gases and aerosols coupled to a high-resolution time-of-flight chemical ionization mass spectrometer (FIGAERO-CIMS). We find on average larger carbon numbers (nC) and lower oxygen-To-carbon (O:C) ratios at the urban sites (nC: 9.8±0.7; O:C: 0.76±0.03; average ±1 standard deviation) compared to the rural (nC: 8.8±0.6; O:C: 0.80±0.05) and mountain stations (nC: 8.1±0.8; O:C: 0.91±0.07), indicative of different emission sources and chemistry. Compounds containing only carbon, hydrogen, and oxygen atoms (CHO) contribute the most to the total OOA mass at the rural sites (79.9±5.2%), in accordance with their proximity to forested areas (66.2±5.5% at the mountain sites and 72.6±4.3% at the urban sites). The largest contribution of nitrogen-containing compounds (CHON) is found at the urban stations (27.1±4.3%), consistent with their higher NOx levels. Moreover, we parametrize OOA volatility (saturation mass concentrations, Csat) using molecular composition information and compare it with the bulk apparent volatility derived from thermal desorption of the OOA particles within the FIGAERO. We find differences in Csat values of up to 1/43 orders of magnitude and variation in thermal desorption profiles (thermograms) across different locations and systems. From our study, we draw the general conclusion that environmental conditions (e.g., ambient temperature) do not directly affect OOA apparent volatility but rather indirectly by influencing the sources and chemistry of the environment and thus the chemical composition. The comprehensive dataset provides results that show the complex thermodynamics and chemistry of OOA and their changes during its lifetime in the atmosphere. We conclude that generally the chemical description of OOA suffices to predict its apparent volatility, at least qualitatively. Our study thus provides new insights that will help guide choices of, e.g., descriptions of OOA volatility in different model frameworks such as air quality models and cloud parcel models.
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6.
  • Lan, Xiaoyu, et al. (författare)
  • Self-Assembly of Diblock Copolymers Containing Thermo- and Photoresponsive Lower Critical Solution Temperature Phase Behavior Polymer with Tunable Assembly Temperature in an Ionic Liquid Mixture
  • 2019
  • Ingår i: ACS Omega. - : American Chemical Society (ACS). - 2470-1343. ; 4:6, s. 11229-11236
  • Tidskriftsartikel (refereegranskat)abstract
    • This work prepared a type of diblock copolymer with thermo- and photosensitivity in ionic liquids (ILs). P(N,N-dimethylacrylamide) (compatible with ILs) was prepared as one segment, while butyl acrylate (BA) and 4-phenylazophenylmethacrylate (AzoMA) were copolymerized as another segment P(AzoMA-r-BA) with stimuli responsiveness. The diblock copolymer showed tunable lower critical micellization temperature (LCMT) in two mixed imidazole ionic liquids. The value of LCMT depends on not only the conformation status of the azo group in copolymers but also the azo group content in copolymers and mixed ratio of ionic liquids. Based on this tunable LCMT, photoinduced micellization/demicellization can be achieved near room temperature by alternate irradiation with visible and ultraviolet light, and it is totally reversible.
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7.
  • Ma, Xiaofeng, et al. (författare)
  • Photo-induced Actuator using Temperature and Light Dual Responsive Azobenzene Containing Ion Gel in Ionic Liquid
  • 2020
  • Ingår i: European Polymer Journal. - : Elsevier. - 0014-3057 .- 1873-1945. ; 123
  • Tidskriftsartikel (refereegranskat)abstract
    • A series of well-defined random copolymers comprising butyl acrylate (BA) and 4-phenylazophenylmethacrylate (AzoMA) (P(AzoMA-r-BA)) are prepared successfully by reversible addition fragmentation chain transfer (RAFT) polymerization. P(AzoMA-r-BA)s show LCST-type phase transition in 1-butyl-3-methylimidazolium bis(trifluoromethanesulfone)amide ([C4mim][NTf2]). LCST depends on the photoisomerization state of azobenzene, as well as on the AzoMA composition in the random copolymers. LCST of (P(cis-AzoMA-r-BA) is significantly higher than that of P(trans-AzoMA-r-BA), because cis-AzoMA and trans-AzoMA behave as solvato-philic and solvato-phobic comonomer, respectively. At a bistable temperature, photo-induced phase separation is completely reversible. Secondly, based on this phenomenon, a thermo- / photo- responsive ion gel (BA-AzoMA ion gel) can be prepared by free radical polymerization of BA and AzoMA using ethylene glycol dimethacrylate (EGDMA) as crosslinker in [C4mim][NTf2]. BA-AzoMA ion gel shows high temperature contraction and low temperature expansion behavior, due to LCST-type phase behavior of polymer system consisting of AzoMA and BA. Contraction temperature of BA-AzoMA ion gel depends on photoisomerization state of the azobenzene group in polymers. At a bistable temperature, photo-induced expansion-contraction is reversible. Finally, a Photo-induced actuator can be realized using BA-AzoMA ion gel at suitable temperatures, featuring reversible bending by alternate irradiating with visible and UV light. The bending behavior is also demonstrated.
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8.
  • Wang, Yuan, et al. (författare)
  • Identification, Tissue Distribution, and Bioaccumulation Potential of Cyclic Perfluorinated Sulfonic Acids Isomers in an Airport Impacted Ecosystem
  • 2016
  • Ingår i: Environmental Science and Technology. - : American Chemical Society (ACS). - 0013-936X .- 1520-5851. ; 50:20, s. 10923-10932
  • Tidskriftsartikel (refereegranskat)abstract
    • The use of cyclic perfluoroalkyl acids as anticorrosive agents in hydraulic fluids remains a poorly characterized source of organofluorine compounds to the environment. Here, we investigated the presence of perfluoroethylenecyclohexanesulfonate (PFECHS) isomers in environmental samples for the first time using a combination of high resolution and tandem mass spectrometry. Five distinct peaks attributed to different isomers of PFECHS and perfluoropropylcyclopentanesulfonate (PFPCPeS) were identified in environmental samples. The sum of PFECHS and PFPCPeS isomers displayed logarithmically decreasing spatial trends in water (1.04-324 ng/L) and sediment samples (
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9.
  • Wu, Lichuan, et al. (författare)
  • Swell impact on wind stress and atmospheric mixing in a regional coupled atmosphere-wave model
  • 2016
  • Ingår i: Journal of Geophysical Research - Oceans. - 2169-9275 .- 2169-9291. ; 121:7, s. 4633-4648
  • Tidskriftsartikel (refereegranskat)abstract
    • Over the ocean, the atmospheric turbulence can be significantly affected by swell waves. Change in the atmospheric turbulence affects the wind stress and atmospheric mixing over swell waves. In this study, the influence of swell on atmospheric mixing and wind stress is introduced into an atmosphere-wave-coupled regional climate model, separately and combined. The swell influence on atmospheric mixing is introduced into the atmospheric mixing length formula by adding a swell-induced contribution to the mixing. The swell influence on the wind stress under wind-following swell, moderate-range wind, and near-neutral and unstable stratification conditions is introduced by changing the roughness length. Five year simulation results indicate that adding the swell influence on atmospheric mixing has limited influence, only slightly increasing the near-surface wind speed; in contrast, adding the swell influence on wind stress reduces the near-surface wind speed. Introducing the wave influence roughness length has a larger influence than does adding the swell influence on mixing. Compared with measurements, adding the swell influence on both atmospheric mixing and wind stress gives the best model performance for the wind speed. The influence varies with wave characteristics for different sea basins. Swell occurs infrequently in the studied area, and one could expect more influence in high-swell-frequency areas (i.e., low-latitude ocean). We conclude that the influence of swell on atmospheric mixing and wind stress should be considered when developing climate models.
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10.
  • Wu, Lichuan, et al. (författare)
  • The impact of waves and sea spray on modelling storm track and development
  • 2015
  • Ingår i: Tellus. Series A, Dynamic meteorology and oceanography. - : Stockholm University Press. - 0280-6495 .- 1600-0870. ; 67
  • Tidskriftsartikel (refereegranskat)abstract
    • In high wind speed conditions, sea spray generated by intensely breaking waves greatly influences the wind stress and heat fluxes. Measurements indicate that the drag coefficient decreases at high wind speeds. The sea spray generation function (SSGF), an important term of wind stress parameterisation at high wind speeds, is usually treated as a function of wind speed/friction velocity. In this study, we introduce a wave-state-dependent SSGF and wave-age-dependent Charnock number into a high wind speed–wind stress parameterisation. The newly proposed wind stress parameterisation and sea spray heat flux parameterisation were applied to an atmosphere–wave coupled model to study the mid-latitude storm development of six storm cases. Compared with measurements from the FINO1 platform in the North Sea, the new wind stress parameterisation can reduce wind speed simulation errors in the high wind speed range. Considering only sea spray impact on wind stress (and not on heat fluxes) will intensify the storms (in terms of minimum sea level pressure and maximum wind speed), but has little effect on the storm tracks. Considering the impact of sea spray on heat fluxes only (not on wind stress) can improve the model performance regarding air temperature, but it has little effect on the storm intensity and storm track performance. If the impact of sea spray on both the wind stress and heat fluxes is taken into account, the model performs best in all experiments for minimum sea level pressure, maximum wind speed and air temperature.
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