The largest database of trusted experimental protocols

D8 advance

Manufactured by Malvern Panalytical
Sourced in Japan

The D8 Advance is an X-ray diffractometer designed for phase identification, quantification, and structural analysis of materials. It features a sealed X-ray tube, a goniometer for precise sample positioning, and a high-resolution detector. The core function of the D8 Advance is to obtain detailed information about the crystallographic structure and composition of various materials.

Automatically generated - may contain errors

7 protocols using d8 advance

1

Crystalline Structure Analysis via XRD

Check if the same lab product or an alternative is used in the 5 most similar protocols
An X-ray diffractometer (D8 ADVANCE, Malvern Instruments, Malvern, UK) under 40 kV and 40 mA with Cu Kα radiation was used to analyze the samples’ crystalline structures. Data were obtained between 4 and 40° (2θ) at a rate of 4°/min. The RC values of the samples were determined with Equation (13): RC (%)=IC / (IC+IA)× 100
where IC and IA refer to the cumulative diffraction intensity of the crystallized region and the amorphous region, respectively.
+ Open protocol
+ Expand
2

Comprehensive Instrumentation for Advanced Materials Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
All the glass wares required in research were washed with dH 2 O and autoclaved at 121 °C for 15 min.
All the instruments used in this study were: Field Emission Scanning Electron Microscopy/FESEM (MIRA3 TESCAN), EXD (MIRA3 TESCAN), Transmission Electron Microscopy/TEM (JEOL JEM-1010), Fourier Transform Infrared spectroscopy/FTIR (FT-IR Perkin Elmer Spectrum 100 spectrometer), X-ray diffraction/XRD (Bruker D8 Advance), Zetasizer (Malvern), Polymerase Chain Reaction/PCR (Thermocycler), ELISA microplate reader (BioTek China), Fluorescence microscope (LSM 510, Carl by Zeiss European Molecular Biology Laboratory), Fluorescence-activated cell sorting (FACS) (BD FACScan, USA), Ultraviolet-Visible (UV-Vis) spectrophotometer (Lambda 950, PerkinElmer, UK), Heating magnetic stirrer (IKA-RCT-B, IKA China), Franz diffusion cell (China).
+ Open protocol
+ Expand
3

X-ray Diffraction Analysis of Adhesive Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cured and dried adhesive samples were ground into powder (particle size around 45 µm) and then tested on an X-ray diffractometer (D8 Advance, Panalytical, Holland). Testing conditions were set as follows: the test target was copper; the scanning speed and angle ranges were 2°/min and 5–60°, respectively. The crystallinity of the adhesive samples was calculated following the report by Pang et al. [22 (link)].
+ Open protocol
+ Expand
4

Chemical and Structural Analysis of Powder Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols
The chemical compositions were determined by using an electron probe micro-analyzer (EPMA) (S-4800, Hitachi, Japan) with an accuracy of >97%.
The powder X-ray diffraction patterns of the samples were registered by using X-ray powder diffractometer (XRD) (D8 Advance) operating at 50 kV and 40 mA in a step size of 0.02° in the range of 10° to 100°, and a X’Pert Pro, PANalytical code was used to do the Rietveld refinement of the XRD patterns with a step size of 0.01° using the same operating voltage and current. The lattice constants a and c were directly obtained from the refinement of the X-ray data using the Jade software.
Differential scanning calorimeter (DSC) is conducted in a Netzch STA 449 F3 Jupiter equipped with a TASC414/4 controller. The instrument is calibrated from a standard list. The sample of the powder (x = 0.15) is loaded into an open alumina crucible. The measurement is performed between ~300 K to ~820 K with a heating rate of 5 K min−1 in Ar atmosphere.
+ Open protocol
+ Expand
5

Comprehensive Chemical and Structural Analysis of Powders

Check if the same lab product or an alternative is used in the 5 most similar protocols
The chemical compositions were determined using an electron probe micro-analyzer (EPMA) (S-4800, Hitachi, Japan) with an accuracy of >97%.
The structural analysis of the powders was made by powder X-ray diffractometer (D8 Advance) operating at 50 kV and 40 mA at Cu Kα radiation (λ = 0.15406 nm) in the 2θ range from 10° to 110° with a step size of 0.02°, and a X'Pert Pro, PANalytical code was used to do the Rietveld refinement of the XRD patterns with a step size of 0.01° using the same operating voltage and current. The lattice constants a and c were directly obtained from the refinement of the XRD patterns using Jade software (Highscore (plus) Software version 4.0 by PANalytical B.V; Almelo, The Netherlands)32 (link) with an error less than 10%.
Differential Scanning calorimeter (DSC) and thermogravimetry (TG) were conducted in a Netzch STA 449 F3 Jupiter equipped with a TASC414/4 controller. The instrument was calibrated from a standard list. The sample of the powder (x = 0) was loaded into an open alumina crucible. The measurement was performed after the samples were heated up to ∼850 K with a heating rate of 5 K min−1 in Ar atmosphere.
+ Open protocol
+ Expand
6

Characterization of Silver Nanoparticle-Chitosan Composite Spheres

Check if the same lab product or an alternative is used in the 5 most similar protocols
The average diameter of the spheres, expressed as mean ± standard deviation, was obtained from the photographs taken by random sampling of approximately 50 individual particles to minimize selection bias. X-ray diffraction (XRD, D8 Advance, PANalytical X’PERT PRO) patterns were obtained at room temperature using Cu K-α radiation (λ=1.5406 Å) with a range of =20° to 80°, and a scanning rate of 0.05 s−1. The FTIR spectra were recorded with a Spectrum RXI FTIR Spectrometer, using KBr pellets, in the range of 400 to 4,000 cm−1, with a resolution of 4 cm−1. The micromorphology of the silver nanoparticles–chitosan composite spheres was analyzed using a SEM (S-2700, Hitachi Ltd., Tolyo, Japan) equipped with an energy dispersive spectrometer. The characterization of the silver nanoparticles was carried out using TEM (FEI Tecnai G2 20 S-Twin) and a UV-Vis absorbance spectrophotometer (Thermo Scientific Spectrascan UV 2700). The silver nanoparticles solution was prepared by adding 20 μL CH3COOH solution and 1 mL dd-H2O to ten silver nanoparticles–chitosan composite spheres, and then vortexing for 35 minutes. The silver nanoparticles–chitosan solution was dropped to grid by a micropipette for TEM analysis report.
+ Open protocol
+ Expand
7

Structural Analysis of Cu2-xSbxGa4Te7

Check if the same lab product or an alternative is used in the 5 most similar protocols
Structural analysis of the powders was made by using a powder X-ray diffractometer (D8 Advance) operating at 50 kV and 40 mA with Cu Kα radiation (λ = 0.15406 nm) in the range from 10° to 110° with a step size of 0.02°, and an X’Pert Pro, PANalytical code was used to do the Rietveld refinement of the XRD patterns of the titled compounds. The lattice constants a and c were directly obtained from the refinement of the XRD patterns using Jade software.
The chemical compositions of the samples Cu2−xSbxGa4Te7 (x = 0, 0.2) were checked using an electron probe micro-analyzer (EPMA) (S-4800, Hitachi, Japan) with an accuracy of >97%.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!