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Dandong Yichuang Pharmaceutical Co Ltd dx 1000 x ray diffractometer
Dx 1000 X Ray Diffractometer, supplied by Dandong Yichuang Pharmaceutical Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/x-ray+diffractometer/diffraction+ray+x/pmc12926580-83-10-13
Average 86 stars, based on 1 article reviews
dx 1000 x ray diffractometer - by Bioz Stars, 2026-09
86/100 stars

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Related Articles

X-ray Diffraction:

Article Title: Hydrogen Removal from Fe at Room Temperature: A Study on Hydrogen Trapping Mechanisms
Article Snippet: .. The sample crystal structure influenced by the charged temperature was investigated by both X-ray diffraction (XRD) (Liaoning Dandong Fangyuan Instrument Co., Ltd., Dandong, China) technique and high-resolution transmission electron microscopy (HRTEM). .. The oxidation behaviors during the EO experiment were analyzed by X-ray photoelectron spectroscopy (XPS) (Thermo Fisher Scientific Inc., Waltham, MA, USA).

Article Title: A continuous adhesion-enhanced osteogenic pathway in artificial scaffold drives cellular infiltration and condensed mineralization for rapid bone regeneration
Article Snippet: Fourier transform infrared (FTIR) spectra were obtained with a Thermo Nicolet 6700 FTIR spectrometer (Madison, WI, USA) at a resolution of 4 cm −1 in reflection mode. .. Wide angle X-ray diffraction (WAXD) test was performed with a DX-1000 X-ray diffractometer (Dandong Fanyuan Instrument Co. LTD, China) at room temperature. ..

Article Title: Response and Failure of Pillar-Backfill Composite Materials Under Cyclic Loading: The Role of Pillar Width.
Article Snippet: .. According to the X-ray diffraction (XRD) (Dandong Tongda Technology Co., Ltd., Dandong, China) analysis in Wang’s experiment, the main mineral compositions of the pillars are: grunerite (51.1%), hematite (14.3%), magnetite (22.5%), and quartz (8.9%); the main mineral compositions of the tailings are: silicon oxide (67.1%), granite (18.8%), and magnetite (8.2%) [25]. ..

Article Title: A web-based platform for real-time stewed beef freshness monitoring: Integrating anthocyanin colorimetric film with deep learning.
Article Snippet: This study developed a web-based online monitoring system for assessing the freshness of stewed beef by integrating an intelligent colorimetric film with deep learning.. A pH-responsive colorimetric film was fabricated using mulberry anthocyanin extract (MAE) as the indicator, gelatin (G) and carboxylated cellulose nanofibers (CCN) as the film-forming matrices, and Mg2+ as the cross-linker.. When applied to monitor stewed beef stored at 4 C, the film exhibited distinct color changes correlated with spoilage indicators.

Article Title: Hydrogen Removal from Fe at Room Temperature: A Study on Hydrogen Trapping Mechanisms.
Article Snippet: .. The sample crystal structure influenced by the charged temperature was investigated by both X-ray diffraction (XRD) (Liaoning Dandong Fangyuan Instrument Co., Ltd., Dandong, China) technique and highresolution transmission electron microscopy (HRTEM). .. The oxidation behaviors during the EO experiment were analyzed by X-ray photoelectron spectroscopy (XPS) (Thermo Fisher Scientific Inc., Waltham, MA, USA).

Transmission Assay:

Article Title: Hydrogen Removal from Fe at Room Temperature: A Study on Hydrogen Trapping Mechanisms
Article Snippet: .. The sample crystal structure influenced by the charged temperature was investigated by both X-ray diffraction (XRD) (Liaoning Dandong Fangyuan Instrument Co., Ltd., Dandong, China) technique and high-resolution transmission electron microscopy (HRTEM). .. The oxidation behaviors during the EO experiment were analyzed by X-ray photoelectron spectroscopy (XPS) (Thermo Fisher Scientific Inc., Waltham, MA, USA).

Article Title: Hydrogen Removal from Fe at Room Temperature: A Study on Hydrogen Trapping Mechanisms.
Article Snippet: .. The sample crystal structure influenced by the charged temperature was investigated by both X-ray diffraction (XRD) (Liaoning Dandong Fangyuan Instrument Co., Ltd., Dandong, China) technique and highresolution transmission electron microscopy (HRTEM). .. The oxidation behaviors during the EO experiment were analyzed by X-ray photoelectron spectroscopy (XPS) (Thermo Fisher Scientific Inc., Waltham, MA, USA).

Electron Microscopy:

Article Title: Hydrogen Removal from Fe at Room Temperature: A Study on Hydrogen Trapping Mechanisms
Article Snippet: .. The sample crystal structure influenced by the charged temperature was investigated by both X-ray diffraction (XRD) (Liaoning Dandong Fangyuan Instrument Co., Ltd., Dandong, China) technique and high-resolution transmission electron microscopy (HRTEM). .. The oxidation behaviors during the EO experiment were analyzed by X-ray photoelectron spectroscopy (XPS) (Thermo Fisher Scientific Inc., Waltham, MA, USA).

Article Title: Hydrogen Removal from Fe at Room Temperature: A Study on Hydrogen Trapping Mechanisms.
Article Snippet: .. The sample crystal structure influenced by the charged temperature was investigated by both X-ray diffraction (XRD) (Liaoning Dandong Fangyuan Instrument Co., Ltd., Dandong, China) technique and highresolution transmission electron microscopy (HRTEM). .. The oxidation behaviors during the EO experiment were analyzed by X-ray photoelectron spectroscopy (XPS) (Thermo Fisher Scientific Inc., Waltham, MA, USA).



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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Image Search Results


Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) Energy-dispersive X-ray spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).

Journal: Bioactive Materials

Article Title: Smart microenvironment-adaptive nanocatalytic hydrogel for sequential antibacterial, anti-inflammatory, and regenerative therapy of biofilm-infected wounds

doi: 10.1016/j.bioactmat.2026.02.043

Figure Lengend Snippet: Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) Energy-dispersive X-ray spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).

Article Snippet: X-ray diffraction (XRD) patterns were conducted on a Bruker D8 ADVANCE X-ray diffractometer using Cu-Kα radiation (λ = 1.5418 Å).

Techniques: Spectroscopy, Concentration Assay