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x ray diffraction xrd patterns  (Rigaku Corporation)


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    Structured Review

    Rigaku Corporation x ray diffraction xrd patterns
    X Ray Diffraction Xrd Patterns, supplied by Rigaku Corporation, used in various techniques. Bioz Stars score: 99/100, based on 6621 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/x+ray+diffraction+patterns/SmartLab+SE/pmc13594647-75-0-11
    Average 99 stars, based on 6621 article reviews
    x ray diffraction xrd patterns - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    X-ray Diffraction:

    Article Title: Coffee ground-derived carbon dots reinforced zein/PVDF electrospun nanofiber membranes with antioxidant and photodynamic antibacterial activities
    Article Snippet: .. Following the methodology established by Yao et al. , the crystal structures of CG-CDs@Zein/PVDF nanofiber membranes with different CG-CD concentrations were investigated using X-ray diffraction (XRD, SmartLab SE, Rigaku, Japan). ..

    Article Title: Microwave power-induced modulation of tigernut ( Cyperus esculentus L.) starch: Insights into structural and functional properties
    Article Snippet: .. A SmartLab SE diffractometer (Rigaku, Japan) with Cu Kα radiation was used to record the X-ray diffraction patterns of the starch samples. ..

    Article Title: Experimental study on the transformation behavior of chlorine and bromine pollutants during gasification of waste printed circuit boards.
    Article Snippet: Chlorinated and brominated flame retardants in waste printed circuit boards (WPCBs) pose a potential risk for the formation of dioxin-like pollutants, yet the phase distribution and migration behavior of Cl and Br during WPCBs gasification remain insufficiently understood.. In this study, the gasification of WPCBs was systematically investigated under a CO2 /O2 (79 %/21 %) atmosphere over 600–900 °C and 0.1–0.4 MPa.. The experimental results indicate that 700 °C at atmosphere pressure provide the most favorable gasification performance within the investigated range, with the highest CO content (86 %), LHVR (3.98 MJ/kg), and gasification efficiency (91 %).

    Article Title: Hydrogel-integrated osteogenic microtissues promote repair of infected intervertebral defects through sequential immunomodulation
    Article Snippet: Hydrogels were freeze-dried, fractured to expose the internal cross-section, sputter-coated with gold, and imaged by field-emission scanning electron microscopy (SEM, Sigma 360, ZEISS, Germany). .. Energy-dispersive X-ray spectroscopy (EDS, Sigma 360, ZEISS, Germany) mapping was used to examine the distribution of C, O, Zn, and P.Fourier transform infrared spectroscopy(FTIR, Nicolet iS50, Thermo Fisher Scientific, USA) was performed with 32 scans in the range of 4000–400 cm −1 at a resolution of 4 cm −1 ; X-ray diffraction patterns (XRD, SmartLab SE, Rigaku Corporation, Japan) were recorded from 5° to 90°. .. Surface morphology, roughness parameters (Ra and Rq), and local nanoscale Young's modulus were characterized using atomic force microscopy(AFM, Dimension Icon, Bruker, Germany).

    Article Title: Regulatory mechanism of leucine-amidated pectin on the gel properties of shrimp surimi as a salt substitute
    Article Snippet: X-ray photoelectron spectroscopy (XPS) analysis was performed using a Thermo Scientific K-Alpha+ spectrometer (Thermo Fisher Co., Ltd., USA) equipped with an Al Kα source (HV = 1486.6 eV), and the C1s peak (284.80 eV) was utilized for charge calibration. .. X-ray diffraction (XRD) patterns of pectin samples were obtained using a Rigaku SmartLab SE diffractometer (Rigaku Co., Ltd., Japan) with Cu Kα radiation (λ = 1.5406 Å). ..

    Article Title: From raw material to functional food: Effect of dry-heat treatment on whole quinoa flour structure and dough rheology, with in vivo hypoglycemic validation at the optimal temperature
    Article Snippet: .. X-ray diffraction patterns were obtained using a Smartlab SE X-ray diffractometer (Rigaku, Japan) operated in step-scan mode. ..

    Starch:

    Article Title: Microwave power-induced modulation of tigernut ( Cyperus esculentus L.) starch: Insights into structural and functional properties
    Article Snippet: .. A SmartLab SE diffractometer (Rigaku, Japan) with Cu Kα radiation was used to record the X-ray diffraction patterns of the starch samples. ..

    Gasification Assay:

    Article Title: Experimental study on the transformation behavior of chlorine and bromine pollutants during gasification of waste printed circuit boards.
    Article Snippet: Chlorinated and brominated flame retardants in waste printed circuit boards (WPCBs) pose a potential risk for the formation of dioxin-like pollutants, yet the phase distribution and migration behavior of Cl and Br during WPCBs gasification remain insufficiently understood.. In this study, the gasification of WPCBs was systematically investigated under a CO2 /O2 (79 %/21 %) atmosphere over 600–900 °C and 0.1–0.4 MPa.. The experimental results indicate that 700 °C at atmosphere pressure provide the most favorable gasification performance within the investigated range, with the highest CO content (86 %), LHVR (3.98 MJ/kg), and gasification efficiency (91 %).

    other:

    Article Title: The application of novel ultrathin iron sulphide nanosheets in the nanotherapy of post-traumatic osteoarthritis
    Article Snippet: The diffraction characteristics of FeSNSs were examined using X-ray diffraction (XRD, Rigaku SmartLab SE, Japan).

    Energy Dispersive X-Ray:

    Article Title: Hydrogel-integrated osteogenic microtissues promote repair of infected intervertebral defects through sequential immunomodulation
    Article Snippet: Hydrogels were freeze-dried, fractured to expose the internal cross-section, sputter-coated with gold, and imaged by field-emission scanning electron microscopy (SEM, Sigma 360, ZEISS, Germany). .. Energy-dispersive X-ray spectroscopy (EDS, Sigma 360, ZEISS, Germany) mapping was used to examine the distribution of C, O, Zn, and P.Fourier transform infrared spectroscopy(FTIR, Nicolet iS50, Thermo Fisher Scientific, USA) was performed with 32 scans in the range of 4000–400 cm −1 at a resolution of 4 cm −1 ; X-ray diffraction patterns (XRD, SmartLab SE, Rigaku Corporation, Japan) were recorded from 5° to 90°. .. Surface morphology, roughness parameters (Ra and Rq), and local nanoscale Young's modulus were characterized using atomic force microscopy(AFM, Dimension Icon, Bruker, Germany).

    Spectroscopy:

    Article Title: Hydrogel-integrated osteogenic microtissues promote repair of infected intervertebral defects through sequential immunomodulation
    Article Snippet: Hydrogels were freeze-dried, fractured to expose the internal cross-section, sputter-coated with gold, and imaged by field-emission scanning electron microscopy (SEM, Sigma 360, ZEISS, Germany). .. Energy-dispersive X-ray spectroscopy (EDS, Sigma 360, ZEISS, Germany) mapping was used to examine the distribution of C, O, Zn, and P.Fourier transform infrared spectroscopy(FTIR, Nicolet iS50, Thermo Fisher Scientific, USA) was performed with 32 scans in the range of 4000–400 cm −1 at a resolution of 4 cm −1 ; X-ray diffraction patterns (XRD, SmartLab SE, Rigaku Corporation, Japan) were recorded from 5° to 90°. .. Surface morphology, roughness parameters (Ra and Rq), and local nanoscale Young's modulus were characterized using atomic force microscopy(AFM, Dimension Icon, Bruker, Germany).

    Infrared:

    Article Title: Hydrogel-integrated osteogenic microtissues promote repair of infected intervertebral defects through sequential immunomodulation
    Article Snippet: Hydrogels were freeze-dried, fractured to expose the internal cross-section, sputter-coated with gold, and imaged by field-emission scanning electron microscopy (SEM, Sigma 360, ZEISS, Germany). .. Energy-dispersive X-ray spectroscopy (EDS, Sigma 360, ZEISS, Germany) mapping was used to examine the distribution of C, O, Zn, and P.Fourier transform infrared spectroscopy(FTIR, Nicolet iS50, Thermo Fisher Scientific, USA) was performed with 32 scans in the range of 4000–400 cm −1 at a resolution of 4 cm −1 ; X-ray diffraction patterns (XRD, SmartLab SE, Rigaku Corporation, Japan) were recorded from 5° to 90°. .. Surface morphology, roughness parameters (Ra and Rq), and local nanoscale Young's modulus were characterized using atomic force microscopy(AFM, Dimension Icon, Bruker, Germany).



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    Rigaku Corporation x ray diffraction xrd patterns
    X Ray Diffraction Xrd Patterns, supplied by Rigaku Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Physicochemical and mechanical characterization of the hydrogel formulations. A) Schematic illustration of the preparation of GA–Zn 2+ /BP@SilMA and incorporation of osteogenic bone microtissues (BO). B) Photographs of the hydrogel precursor before and after ultraviolet. C) Scanning electron microscopy (SEM) images of SilMA, GA–Zn 2+ @SilMA, GA–Zn 2+ /BP@SilMA, and GA–Zn 2+ /BP/BO@SilMA hydrogels. D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) elemental maps of C, O, P, and Zn in the composite hydrogel. E) Fourier-transform infrared spectroscopy (FTIR) spectra of the different hydrogel formulations. F) X-ray <t>diffraction</t> (XRD) patterns of the different hydrogel formulations. G) Atomic force microscopy (AFM) force–separation curves. H) Zn 2+ release profile. I) Degradation behavior of the hydrogel. J) Young's modulus of the different hydrogel formulations. Data are presented as mean ± SD. *p < 0.05 and ****p < 0.0001.
    X Ray Diffraction Patterns, supplied by Rigaku Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Physicochemical and mechanical characterization of the hydrogel formulations. A) Schematic illustration of the preparation of GA–Zn 2+ /BP@SilMA and incorporation of osteogenic bone microtissues (BO). B) Photographs of the hydrogel precursor before and after ultraviolet. C) Scanning electron microscopy (SEM) images of SilMA, GA–Zn 2+ @SilMA, GA–Zn 2+ /BP@SilMA, and GA–Zn 2+ /BP/BO@SilMA hydrogels. D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) elemental maps of C, O, P, and Zn in the composite hydrogel. E) Fourier-transform infrared spectroscopy (FTIR) spectra of the different hydrogel formulations. F) X-ray <t>diffraction</t> (XRD) patterns of the different hydrogel formulations. G) Atomic force microscopy (AFM) force–separation curves. H) Zn 2+ release profile. I) Degradation behavior of the hydrogel. J) Young's modulus of the different hydrogel formulations. Data are presented as mean ± SD. *p < 0.05 and ****p < 0.0001.
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    Rigaku Corporation powder x ray diffraction pxrd patterns
    Solid‐state characterization of L ‐TASe and D ‐TASe crystals. (a) Experimental <t>PXRD</t> patterns of L ‐TASe and D ‐TASe and simulated pattern from SCXRD data, confirming phase purity and crystallinity. (b) FTIR spectra of L ‐TASe and D ‐TASe , showing amide I and amide II vibrations. (c) Solid‐state CD and absorption spectra of L ‐TASe and D ‐TASe . Mirror‐image Cotton effects confirm their enantiomeric relationship. (d) TGA curves of L ‐TASe and D ‐TASe , showing thermal stability up to 290°C. (e) <t>PXRD</t> patterns of L ‐TASe after 30‐day immersion in aqueous media at pH 2.0 – 7.8, demonstrating chemical robustness. (f) CO 2 adsorption‐desorption isotherms of L ‐TASe at 273 K. Inset: pore size distribution, revealing microporous features.
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    Image Search Results


    Physicochemical and mechanical characterization of the hydrogel formulations. A) Schematic illustration of the preparation of GA–Zn 2+ /BP@SilMA and incorporation of osteogenic bone microtissues (BO). B) Photographs of the hydrogel precursor before and after ultraviolet. C) Scanning electron microscopy (SEM) images of SilMA, GA–Zn 2+ @SilMA, GA–Zn 2+ /BP@SilMA, and GA–Zn 2+ /BP/BO@SilMA hydrogels. D) Energy-dispersive X-ray spectroscopy (EDS) elemental maps of C, O, P, and Zn in the composite hydrogel. E) Fourier-transform infrared spectroscopy (FTIR) spectra of the different hydrogel formulations. F) X-ray diffraction (XRD) patterns of the different hydrogel formulations. G) Atomic force microscopy (AFM) force–separation curves. H) Zn 2+ release profile. I) Degradation behavior of the hydrogel. J) Young's modulus of the different hydrogel formulations. Data are presented as mean ± SD. *p < 0.05 and ****p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Hydrogel-integrated osteogenic microtissues promote repair of infected intervertebral defects through sequential immunomodulation

    doi: 10.1016/j.mtbio.2026.103657

    Figure Lengend Snippet: Physicochemical and mechanical characterization of the hydrogel formulations. A) Schematic illustration of the preparation of GA–Zn 2+ /BP@SilMA and incorporation of osteogenic bone microtissues (BO). B) Photographs of the hydrogel precursor before and after ultraviolet. C) Scanning electron microscopy (SEM) images of SilMA, GA–Zn 2+ @SilMA, GA–Zn 2+ /BP@SilMA, and GA–Zn 2+ /BP/BO@SilMA hydrogels. D) Energy-dispersive X-ray spectroscopy (EDS) elemental maps of C, O, P, and Zn in the composite hydrogel. E) Fourier-transform infrared spectroscopy (FTIR) spectra of the different hydrogel formulations. F) X-ray diffraction (XRD) patterns of the different hydrogel formulations. G) Atomic force microscopy (AFM) force–separation curves. H) Zn 2+ release profile. I) Degradation behavior of the hydrogel. J) Young's modulus of the different hydrogel formulations. Data are presented as mean ± SD. *p < 0.05 and ****p < 0.0001.

    Article Snippet: Energy-dispersive X-ray spectroscopy (EDS, Sigma 360, ZEISS, Germany) mapping was used to examine the distribution of C, O, Zn, and P.Fourier transform infrared spectroscopy(FTIR, Nicolet iS50, Thermo Fisher Scientific, USA) was performed with 32 scans in the range of 4000–400 cm −1 at a resolution of 4 cm −1 ; X-ray diffraction patterns (XRD, SmartLab SE, Rigaku Corporation, Japan) were recorded from 5° to 90°.

    Techniques: Scanning Electron Microscopy, Energy Dispersive X-Ray, Spectroscopy, Fourier Transform Infrared Spectroscopy, Microscopy

    Solid‐state characterization of L ‐TASe and D ‐TASe crystals. (a) Experimental PXRD patterns of L ‐TASe and D ‐TASe and simulated pattern from SCXRD data, confirming phase purity and crystallinity. (b) FTIR spectra of L ‐TASe and D ‐TASe , showing amide I and amide II vibrations. (c) Solid‐state CD and absorption spectra of L ‐TASe and D ‐TASe . Mirror‐image Cotton effects confirm their enantiomeric relationship. (d) TGA curves of L ‐TASe and D ‐TASe , showing thermal stability up to 290°C. (e) PXRD patterns of L ‐TASe after 30‐day immersion in aqueous media at pH 2.0 – 7.8, demonstrating chemical robustness. (f) CO 2 adsorption‐desorption isotherms of L ‐TASe at 273 K. Inset: pore size distribution, revealing microporous features.

    Journal: Advanced Science

    Article Title: Supramolecular Chiral Assemblies from Benzoselenadiazole‐Alanine‐Acylhydrazone Conjugates Enable Cardioprotection

    doi: 10.1002/advs.77953

    Figure Lengend Snippet: Solid‐state characterization of L ‐TASe and D ‐TASe crystals. (a) Experimental PXRD patterns of L ‐TASe and D ‐TASe and simulated pattern from SCXRD data, confirming phase purity and crystallinity. (b) FTIR spectra of L ‐TASe and D ‐TASe , showing amide I and amide II vibrations. (c) Solid‐state CD and absorption spectra of L ‐TASe and D ‐TASe . Mirror‐image Cotton effects confirm their enantiomeric relationship. (d) TGA curves of L ‐TASe and D ‐TASe , showing thermal stability up to 290°C. (e) PXRD patterns of L ‐TASe after 30‐day immersion in aqueous media at pH 2.0 – 7.8, demonstrating chemical robustness. (f) CO 2 adsorption‐desorption isotherms of L ‐TASe at 273 K. Inset: pore size distribution, revealing microporous features.

    Article Snippet: Powder x‐ray diffraction (PXRD) patterns were recorded on a SmartLab diffractometer, Rigaku, Japan, using Cu Kα radiation at room temperature with a step size of 0.02°.

    Techniques: Stability, Adsorption, Pore Size