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Raxis 4 imaging plate detector

Manufactured by Rigaku
Sourced in Japan

The RAXIS-IV is an imaging plate detector designed for X-ray diffraction analysis. It is capable of detecting and recording X-ray diffraction patterns produced by crystalline samples. The detector uses an imaging plate technology to capture the diffraction data, which can then be processed and analyzed using appropriate software.

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3 protocols using raxis 4 imaging plate detector

1

Structural Analysis via Synchrotron X-Ray Scattering

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X-ray total scattering data
were collected on a Rigaku RAXIS-IV imaging plate detector at the
BL10XU beamline in SPring-8 (λ = 0.19909 Å, determined
using CeO2). The exposure time was 600 s. The sample was
packed in a Kapton capillary (ϕ 1 mm). After roughly determining
the structure using this PDF data (Qmax = 20.0 Å–1), further analysis was performed
using the data collected at the BL08W beamline in SPring-8 (λ
= 0.1076 Å, Qmax = 29.0 Å–1). In addition to these PDF data, synchrotron XRD
data were collected using PILATUS 100K semiconductor detectors at
the BL5S2 beamline (beam size = 0.5 mm × 0.5 mm, λ = 1.29945
Å) at 25 °C. The crystal structure was determined using
the EXPO2014 program.
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2

Powder X-ray Diffraction Analysis

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Small angle powder X-ray diffraction patterns of the pristine samples in powder form were recorded with the aid of “Lindemann” type glass capillaries (OD = 0.7 mm) on a Rigaku (Tokyo, Japan) R-AXIS IV Imaging Plate Detector combined with a RU-H3R Rotating Copper Anode X-ray Generator (λ = 0.154 nm). Wide angle pXRD measurements were carried out on a Bruker (Billerica, MA, USA) X-ray system (D8-Advance diffractometer equipped with a LynxEye type detector). Cu Kα radiation (λ = 0.154 nm), operated at 40 kV and 40 mA, was used. Data were collected over the 2θ range from 0° to 160° at a scanning speed of 0.35 s/step and a step size of 0.02°.
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3

X-ray Diffraction Analysis of PHCP Crystal Structure

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The X‐ray diffraction experiment on a PHCP crystal was carried out on a Rigaku Micromax‐007 rotating anode X‐ray generator with a Cu target equipped with an R‐AXIS IV++ imaging plate detector (Rigaku, Japan). The crystal was flash‐cooled at −173°C in a stream of cold nitrogen, using following the cryoprotectant solution: 0.05M sodium citrate, 30% (w/v) PEG 4,000, and 0.1M Tris‐HCl (pH 8.1). A total of 270 images were collected for the PHCP crystal at a camera length of 150 mm and an oscillation angle of 1.0°. The PHCP crystal diffracted to a maximal resolution of 1.89 Å (Table 2). The diffraction data sets were processed using CrystalClear (Rigaku, Japan). The PHCP crystal belonged to the space group P21221 (a = 54.24 Å, b = 72.92 Å, c = 132.37 Å), and had four PHCP molecules in an asymmetric unit, with a Matthews coefficient of 2.15 Å3/Da, which corresponds to a solvent content of 42.7%.34
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