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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/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: Hydration channel engineering in Tröger’s base-POP membranes for mono/multivalent cation and anion discrimination
    Article Snippet: Attenuated total reflection infrared-fourier transform infrared reflection characterization (Thermo Fisher Scientific Nicolet iS20) and XPS characterization (Thermo Scientific K-Alpha) were conducted to investigate the molecular structure and chemical composition of PIM-DT_X membranes. .. X-ray diffraction patterns were obtained using a Rigaku SmartLab SE diffractometer with Cu radiation. ..

    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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    Structural, chemical, and electronic modulation in MoS 2 films induced by vdW‐gap molecular confinement. (a) Schematic of the molecule‐confined MoS 2 structure, illustrating the insertion of molecules within the vdW gap. <t>(b)</t> <t>X‐ray</t> <t>diffraction</t> patterns of H 2 O‐MoS 2 and EtOH‐MoS 2 films under different annealing temperatures (RT, 200°C, and 300°C), showing the molecule‐dependent evolution of interlayer spacing. (c) Temperature‐dependent phase transition of EtOH‐MoS 2 from 1T to 2H, identified by Mo 3d XPS spectra. (d) C 1s XPS spectra revealing the presence and chemical state of confined molecules. (e) Surface potential variation measured by KPFM as a function of annealing temperature, showing thermally activated electronic modulation. (f) Work function changes of H 2 O‐ and EtOH‐ MoS 2 films after annealing at 200°C, demonstrating an upward Fermi‐level shift and the associated electron doping effect.
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    Structural, chemical, and electronic modulation in MoS 2 films induced by vdW‐gap molecular confinement. (a) Schematic of the molecule‐confined MoS 2 structure, illustrating the insertion of molecules within the vdW gap. <t>(b)</t> <t>X‐ray</t> <t>diffraction</t> patterns of H 2 O‐MoS 2 and EtOH‐MoS 2 films under different annealing temperatures (RT, 200°C, and 300°C), showing the molecule‐dependent evolution of interlayer spacing. (c) Temperature‐dependent phase transition of EtOH‐MoS 2 from 1T to 2H, identified by Mo 3d XPS spectra. (d) C 1s XPS spectra revealing the presence and chemical state of confined molecules. (e) Surface potential variation measured by KPFM as a function of annealing temperature, showing thermally activated electronic modulation. (f) Work function changes of H 2 O‐ and EtOH‐ MoS 2 films after annealing at 200°C, demonstrating an upward Fermi‐level shift and the associated electron doping effect.
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    Structural, chemical, and electronic modulation in MoS 2 films induced by vdW‐gap molecular confinement. (a) Schematic of the molecule‐confined MoS 2 structure, illustrating the insertion of molecules within the vdW gap. <t>(b)</t> <t>X‐ray</t> <t>diffraction</t> patterns of H 2 O‐MoS 2 and EtOH‐MoS 2 films under different annealing temperatures (RT, 200°C, and 300°C), showing the molecule‐dependent evolution of interlayer spacing. (c) Temperature‐dependent phase transition of EtOH‐MoS 2 from 1T to 2H, identified by Mo 3d XPS spectra. (d) C 1s XPS spectra revealing the presence and chemical state of confined molecules. (e) Surface potential variation measured by KPFM as a function of annealing temperature, showing thermally activated electronic modulation. (f) Work function changes of H 2 O‐ and EtOH‐ MoS 2 films after annealing at 200°C, demonstrating an upward Fermi‐level shift and the associated electron doping effect.
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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 x ray diffraction
    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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    Image Search Results


    Structural, chemical, and electronic modulation in MoS 2 films induced by vdW‐gap molecular confinement. (a) Schematic of the molecule‐confined MoS 2 structure, illustrating the insertion of molecules within the vdW gap. (b) X‐ray diffraction patterns of H 2 O‐MoS 2 and EtOH‐MoS 2 films under different annealing temperatures (RT, 200°C, and 300°C), showing the molecule‐dependent evolution of interlayer spacing. (c) Temperature‐dependent phase transition of EtOH‐MoS 2 from 1T to 2H, identified by Mo 3d XPS spectra. (d) C 1s XPS spectra revealing the presence and chemical state of confined molecules. (e) Surface potential variation measured by KPFM as a function of annealing temperature, showing thermally activated electronic modulation. (f) Work function changes of H 2 O‐ and EtOH‐ MoS 2 films after annealing at 200°C, demonstrating an upward Fermi‐level shift and the associated electron doping effect.

    Journal: Advanced Science

    Article Title: Van der Waals Gap‐Confined Molecular Engineering of MoS 2 for Selectivity‐Enhanced and Humidity‐Tolerant Gas Sensing

    doi: 10.1002/advs.78072

    Figure Lengend Snippet: Structural, chemical, and electronic modulation in MoS 2 films induced by vdW‐gap molecular confinement. (a) Schematic of the molecule‐confined MoS 2 structure, illustrating the insertion of molecules within the vdW gap. (b) X‐ray diffraction patterns of H 2 O‐MoS 2 and EtOH‐MoS 2 films under different annealing temperatures (RT, 200°C, and 300°C), showing the molecule‐dependent evolution of interlayer spacing. (c) Temperature‐dependent phase transition of EtOH‐MoS 2 from 1T to 2H, identified by Mo 3d XPS spectra. (d) C 1s XPS spectra revealing the presence and chemical state of confined molecules. (e) Surface potential variation measured by KPFM as a function of annealing temperature, showing thermally activated electronic modulation. (f) Work function changes of H 2 O‐ and EtOH‐ MoS 2 films after annealing at 200°C, demonstrating an upward Fermi‐level shift and the associated electron doping effect.

    Article Snippet: To examine changes in the interlayer spacing and crystallographic structure, x‐ray diffraction (XRD) analysis was conducted using a SmartLab diffractometer (Rigaku) with Cu Kα radiation (λ = 0.15412 nm).

    Techniques: Sublimation

    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