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x ray diffraction xrd patterns  (Rigaku Corporation)


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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 35307 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/x+ray+diffraction+patterns/Ultima+IV/pmc13656018-75-0-11
    Average 99 stars, based on 35307 article reviews
    x ray diffraction xrd patterns - by Bioz Stars, 2026-10
    99/100 stars

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    Fourier Transform Infrared Spectroscopy:

    Article Title: Study on the coupling reaction of mixed dibasic acid dimethyl esters with propylene carbonate catalyzed by diacidic ionic liquids
    Article Snippet: .. Gas chromatograph (GC9790 plus, Zhejiang Fuli Analytical Instruments Co., Ltd, China); Fourier transform infrared spectrometer (TENSOR II, Bruker, Germany); Nuclear magnetic resonance spectrometer (AVANCE III, Bruker, Germany); Thermogravimetric analyzer (TGA55, TA, USA); X-ray diffractometer (Ultima IV, Rigaku, Japan); differential scanning calorimeter (TA250, HITACHI, Japan); Gel permeation chromatograph (Agilent 1260, Agilent, USA). ..

    Nuclear Magnetic Resonance:

    Article Title: Study on the coupling reaction of mixed dibasic acid dimethyl esters with propylene carbonate catalyzed by diacidic ionic liquids
    Article Snippet: .. Gas chromatograph (GC9790 plus, Zhejiang Fuli Analytical Instruments Co., Ltd, China); Fourier transform infrared spectrometer (TENSOR II, Bruker, Germany); Nuclear magnetic resonance spectrometer (AVANCE III, Bruker, Germany); Thermogravimetric analyzer (TGA55, TA, USA); X-ray diffractometer (Ultima IV, Rigaku, Japan); differential scanning calorimeter (TA250, HITACHI, Japan); Gel permeation chromatograph (Agilent 1260, Agilent, USA). ..

    X-ray Diffraction:

    Article Title: Molecularly imprinted polymer SiO 2 nanostructures combined with anthocyanin from purple sweet potato peel for on-site colorimetric sensing of benzoic acid in milk
    Article Snippet: UV-visible absorption spectra were obtained with a Jasco V670 UV-vis spectrophotometer (Japan). .. X-ray diffraction (XRD) patterns were collected on an Ultima IV diffractometer (Rigaku, Japan). .. The surface morphologies were characterized by scanning electron microscopy (JSM-IT200, JEOL, Japan).

    Article Title: Spatially deterministic nucleation of 2D semiconductors by etching flux.
    Article Snippet: The XPS peaks were fitted using Thermo Avantage software. .. To examine the phase and crystal structure changes of HfO2 depending on annealing temperature (350–850 °C), grazing incidence X-ray diffraction (Ultima IV, RIGAKU) measurement was performed with Cu-Kα radiation (λ = 1.541 Å). ..

    Article Title: CoFe 2 O 4 prepared from cobalt-doped coal-gangue-leached iron as an effective peroxymonosulfate activator to degrade rhodamine B: preparation, application and degradation mechanism
    Article Snippet: .. The phase of the catalyst was characterized with an X-ray powder diffractometer (XRD, Rigaku Ultima IV, Japan), using Cu Kα radiation, with data collection in a continuous scanning angle of 10°–80°. .. The surface morphology and microstructure of the catalyst were characterized with a scanning electron microscope (SEM, ZEISS Sigma 300, GER) equipped with an energy-dispersive X-ray spectroscopy instrument (EDS, Smartedx, GER).

    Article Title: Efficient and stable carbon capture from industrial flue gas under humid conditions using amine-functionalized Zr-MOF-808 through statistical process design
    Article Snippet: .. Powder X-ray diffraction (PXRD) was conducted using the Rigaku ULTIMA-IV model with a Cu X-ray source ( λ = 0.154 nm) to analyze phase formation and crystallinity over a 2 θ range of 5–40°. .. Field-emission scanning electron microscopy (FE-SEM) was conducted using the FEI Apreo LoVac, which features integrated STEM and a DBS detector to examine the surface morphology of the adsorbents.

    Article Title: Soluble Nanomedicine Against Soluble Neurosensitizers to Effectively Relieve Osteoarthritis Pain and Joint Damage
    Article Snippet: Deconvolution of the narrow‐scan XPS spectra was done with Thermo Avantage software (version 5.991). .. XRD was measured by the Rigaku Ultima IV x‐ray diffractometer instrument. ..

    Article Title: Spatiotemporal Regulation of Hierarchical Assembly of Hydroxyapatite for Enamel Remineralization
    Article Snippet: .. The XRD spectra of the samples were acquired using a Rigaku Ultima IV diffractometer (Rigaku Corporation, Japan) with Cu Kα radiation (λ = 1.542 Å). ..

    Article Title: Influence of aliovalent doping on the La 2− x Sr x Ni 1− y Cu y O 4 for catalytic dry reforming of methane
    Article Snippet: .. The crystalline structure of the synthesized materials was examined using powder XRD on a Rigaku Ultima IV diffractometer equipped with Cu Kα radiation ( λ = 1.5418 Å). ..

    Synthesized:

    Article Title: Influence of aliovalent doping on the La 2− x Sr x Ni 1− y Cu y O 4 for catalytic dry reforming of methane
    Article Snippet: .. The crystalline structure of the synthesized materials was examined using powder XRD on a Rigaku Ultima IV diffractometer equipped with Cu Kα radiation ( λ = 1.5418 Å). ..



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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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    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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    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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    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