In Situ SAXS Analysis of Interfacial Wetting on Nanorough Surfaces

2012 ◽  
Vol 65 (3) ◽  
pp. 254 ◽  
Author(s):  
Jacky K. L. Cho ◽  
Lauren A. Palmer ◽  
Alex H.-F. Wu ◽  
Irving I. Liaw ◽  
David Cookson ◽  
...  

Superhydrophobic surfaces were fabricated through a nanoparticle sol-gel process in the presence of a mono-disperse latex particle. By varying precursor nanoparticle size, surfaces of varying degrees of nanoroughness but controlled macro-roughness were produced, all of which exhibited superhydrophobic properties (θwater >160°, sliding angle <10°). These were immersed in water and studied in situ using synchrotron small angle X-ray scattering where the percentage interface under wetting (in contact with liquid) was directly quantified and found to agree well with traditional Cassie equations. Wetting studies in sodium dodecyl sulphate solutions of decreasing surface tension highlighting surfaces of increased hierarchical roughness (pseudo-fractal dimension ~2.5) contained significant quantity of entrapped air even at fluid surface tensions down to 37 mN m–1.

Metals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1198
Author(s):  
Li Li ◽  
Leyun Wang ◽  
Jie Wang ◽  
Huan Zhang ◽  
Qingchun Zhu ◽  
...  

In this study, in situ synchrotron X-ray experiments with wide-angle X-ray scattering (WAXS) and small-angle X-ray scattering (SAXS) detectors were performed on two pure magnesium materials produced by powder metallurgy. According to SAXS analysis, each of the two materials has a porosity of less than 0.5%. Line broadening analysis was performed on diffraction patterns collected by WAXS to analyze the dislocation evolution during material deformation. In both materials, <a>-type dislocation activities dominate the tensile deformation. The influence of grain size and texture on the different tensile behaviors of these two materials is also discussed.


2015 ◽  
Vol 17 (15) ◽  
pp. 9841-9848 ◽  
Author(s):  
Moheb Nayeri ◽  
Kim Nygård ◽  
Maths Karlsson ◽  
Manuel Maréchal ◽  
Manfred Burghammer ◽  
...  

Structural and chemical changes during the sol–gel synthesis of silica using an ionic liquid are investigatedin situand simultaneously by X-ray scattering and μ-Raman spectroscopy.


2019 ◽  
Vol 624 ◽  
pp. A136
Author(s):  
S. P. Thompson ◽  
A. Herlihy ◽  
C. A. Murray ◽  
A. R. Baker ◽  
S. J. Day ◽  
...  

Context. Laboratory analogues can provide physical constraints to the interpretation of astronomical observations of cosmic dust but clearly do not experience the same formation conditions. To distinguish between properties intrinsic to the material and properties imprinted by their means of formation requires extensive characterisation. Aims. Sol–gel methods can produce amorphous silicates with potentially high reproducibility, but often require long drying times (24+ h) at elevated temperatures in air, controlled atmosphere, or vacuum. We investigate the possibility that microwave drying can be used to form amorphous silicate on a timescale of ∼10 min and characterise their structural and spectroscopic properties relative to silicates produced by other drying methods. Methods. Microwave-dried amorphous MgSiO3, Fe0.1Mg0.9SiO3 and Mg2SiO4 are characterised using X-ray powder diffraction, total X-ray scattering, small angle X-ray scattering and mid-IR FTIR spectroscopy, and compared to samples produced from the same gels but dried in-air and under vacuum. The development of crystalline structure in the microwave-dried silicates via thermal annealing up to 999°C is also investigated using in situ X-ray powder diffraction. Results. At the inter-atomic level the silicate structures are largely independent of drying method, however larger-scale structured domains, ranging from a ∼few × 10 Å to ∼100’s Å in size, are observed. These are ordered as mass fractals with discernible variation caused by the drying processes. The mid-IR 10 μm band profile is also found to be influenced by the drying process, likely due to the way removal of water and bonded OH influences the distribution of tetrahedral species. However, microwave drying also allows Fe to be easily incorporated into the silicate structure. In situ annealing shows that for amorphous MgSiO3 crystalline forsterite, enstatite and cristobalite are high temperature phases, while for Mg2SiO4 forsterite crystallises at lower temperatures followed by cristobalite at high temperature. For Fe0.1Mg0.9SiO3 the crystallisation temperature is significantly increased and only forsterite is observed. Crystalline SiO2 may be diagnostic of Mg-rich, Fe-poor grain mineralogies. The results are discussed in relation to the different thermal conditions required for dust to crystallise within protoplanetary disk lifetimes. Conclusions. Sol–gel microwave drying provides a fast and easy method of producing amorphous Mg- and Fe,Mg-silicates of both pyroxene and olivine compositions. Their structure and spectroscopic characteristics although similar to silicates produced using other drying methods, exhibit subtle variations which are particularly manifest spectroscopically in the mid-IR, and structurally over medium- and long-range length scales.


2009 ◽  
Vol 113 (23) ◽  
pp. 10021-10028 ◽  
Author(s):  
Twilight Barnardo ◽  
Kristin Hoydalsvik ◽  
Rudolf Winter ◽  
Chris M. Martin ◽  
Graham F. Clark

2020 ◽  
pp. 089270572093593
Author(s):  
Anna Lecticia Martinez Martinez Toledo ◽  
Elton Jorge da Rocha Rodrigues ◽  
Maxwell de Paula Cavalcante ◽  
José Carlos Dutra Filho ◽  
Maria Inês Bruno Tavares

Silica-based (SiO2) poly(3-hydroxybutyrate) (PHB) nanocomposites were obtained via an in situ sol–gel route in three distinct particle concentrations (1, 5, and 7.5% by weight of PHB). The polymer hybrids formed were analyzed via wide-angle X-ray diffraction (WAXD), small-angle X-ray scattering (SAXS), Fourier transform infrared (FTIR) spectroscopy, and time-domain nuclear magnetic resonance relaxometry (TD-NMR). The SiO2 inorganic structure displayed surface fractal features at low concentration (1 wt%) and denser agglomerates at higher concentrations (5 and 7.5 wt%). FTIR and SAXS results confirmed the formation of the inorganic matrix amid the polymer chains with different levels of distribution and organization. WAXD and TD-NMR results suggested the SiO2 influence on the PHB crystallinity degree, which was reflected on the polymer’s molecular dynamics with a nonlinear dependence of particles concentration in the PHB matrix.


2020 ◽  
Author(s):  
Susanne Seibt ◽  
Timothy Ryan

With the advent of new in situ structural characterisation techniques including X-ray scattering, there has been an increased interest in investigations of the reaction kinetics of nucleation and growth of nanoparticles as well as self-assembly processes. In this chapter, we discuss the applications of microfluidic devices specifically developed for the investigation of time resolved analysis of growth kinetics and structural evolution of nanoparticles and nanofibers. We focus on the design considerations required for spectrometry and SAXS analysis, the advantages of using a combination of SAXS and microfluidics for these measurements, and discuss in an applied fashion the use of these devices for time-resolved research.


2013 ◽  
Vol 596 ◽  
pp. 50-54 ◽  
Author(s):  
Hiroki Uehara ◽  
Masaki Kakiage ◽  
Hidekazu Tanaka ◽  
Takeshi Yamanobe

Structural deformation during uniaxial drawing of polyethylene-block-polystyrene (PE-b-PS) copolymer film was analyzed by in-situ small angle X-ray scattering (SAXS) measurement. The PE-b-PS film was prepared by solution casting, followed by isothermally crystallizing from melt. The obtained film exhibits the characteristic bicontinuous crystalline/amorphous morphology. Initial stage of uniaxial drawing induces the orientation of such crystalline/amorphous phases, but these phase separation is destroyed in the latter stage. In contrast, solvent swelling treatment successfully induces the orientation of crystalline/amorphous phases with keeping the phase continuity.


2019 ◽  
Author(s):  
Christian Prehal ◽  
Aleksej Samojlov ◽  
Manfred Nachtnebel ◽  
Manfred Kriechbaum ◽  
Heinz Amenitsch ◽  
...  

<b>Here we use in situ small and wide angle X-ray scattering to elucidate unexpected mechanistic insights of the O2 reduction mechanism in Li-O2 batteries.<br></b>


Sign in / Sign up

Export Citation Format

Share Document