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Pw3830 x ray generator

Manufactured by Malvern Panalytical
Sourced in Austria

The PW3830 X-ray generator is a high-performance device designed for laboratory use. It produces X-rays for various analytical techniques. The generator provides a stable and reliable source of X-rays to support scientific research and industrial applications.

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9 protocols using pw3830 x ray generator

1

SAXS Analysis of Starch Samples

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SAXS experiments were performed on a SAXSess small-angle X-ray scattering system (Anton-Paar, Austria) equipped with a PW3830 X-ray generator (PANalytical), operated at 50 mA and 40 kV, using Cu-Kα radiation with a wavelength of 0.1542 nm as the X-ray source. The samples (ca. 60% MC) used for the SAXS measurement were prepared by premixing the starches with added water in glass vials and were equilibrated at 20 °C for 24 h before the analysis. Each sample was placed in a paste sample cell and was exposed at the incident X-ray monochromatic beam for 5 min.
The data, recorded using an image plate, were collected by the IP Reader software with a PerkinElmer storage phosphor system. All data were normalized, and the background intensity and smeared intensity were removed using the SAXSquant 3.0 software for further analysis.
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2

X-Ray Diffraction Analysis of Crystalline Samples

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X-ray diffraction patterns were collected
in reflection using a Philips-Norelco wide-range goniometer and scintillation
counter, equipped with an Advanced Materials Research graphite focusing
monochromator. Cu Kα radiation (λ = 0.15418 nm) was produced
via a PANalytical PW3830 X-ray generator with a long-fine-focus Cu
tube. Angular calibrations were performed using a quartz reference
standard. Samples were deposited as a loose powder (∼0.5 mm
deep) onto carbon tape, supported on a glass microscope slide. Sample
crystallinity was assessed by the presence or absence of strong Bragg
reflections.35
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3

Phase Transformation of SPTS Explored

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The phase transformation of SPTS from semisolid to liquid and from precursor to gel was comprehensively explored by visual, polarized light microscope (PLM, Mshot Instruments Ltd, Guangzhou, China) and small angle X-ray scattering (SAXS, SAXSee, Anton Paar, UK) method. For the visual test, each SPTS@hard capsules was placed in vials with 5 mL distilled water or hydrochloric acid solution (pH 1.2) under 37 ± 0.5 °C. Changes of appearance at certain time intervals were photographic recorded.
The dynamic phase transformation process of SPTSs upon contacting with distilled water or PBS was observed with PLM at 37 ± 0.5 °C by observing the birefringence texture. SPTS@hard capsules of DOXY and MLX were withdrawn from distilled water and PBS respectively at different time intervals. The photographs were taken using a MD50 digital camera.
The crystalline structures of the SPTSs were characterized by the SAXS at 37 ± 0.5 °C. Samples were measured at 50 mA and 40 kV using a PW3830 X-ray generator (PANalytical) with the X-ray source of Cu Kα radiation (λ = 0.1542 nm). The intensity versus scattering factor (q) was recorded.
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4

SAXS Analysis of Gel Structure

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A SAXSess small-angle X-ray scattering system (Anton-Paar GmbH, Glaz, Austria) equipped with a PW3830 X-ray generator (PANalytical) was used to study the gel structure. Measurements were performed according to a previously described method [28 (link),29 (link)]. Samples were measured at 50 mA and 40 kV using a Cu Kα radiation source (λ = 0.1542 nm). Each gel sample was stored at 4 °C for 24 h prior to analysis. The data recorded using an image plate were analyzed by the IP Reader software with a Perkin Elmer storage phosphor system. All data were normalized, and the background and smeared intensities were removed using the SAXS quant 3.0 software for further analysis.
The relationship between q and θ was determined according to the following equation [30 (link)]:
where θ means the scattering angle.
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5

Structural Analysis by SAXS

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The semi-crystalline structure was determined by Small angle X-ray scattering (SAXS) analysis (32 (link)). SAXS measurements were conducted on SAXSess small angle X-ray scattering system (Anton Paar, Graz, Austria) which was equipped with a PW3830 X-ray generator (PANalytical) using Cu Kα radiation (λ = 0.1542 nm).
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6

SAXS Analysis of Nanocomposite Films

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The nanocomposites were cut into strips for SAXS experiment using a SAXSess camera (Anton-Paar, Graz, Austria). A PW3830 X-ray generator with a long fine focus sealed glass X-ray tube (PANalytical) was utilized, and the operating voltage and current were 40 kV and 50 mA, respectively. A block collimator provided an intense monochromatic primary beam (Cu-Kα, λ = 0.1542 nm). The films were placed in the sample holder along the line shape X-ray beam in the evacuated camera housing. The sample-to-detector distance was 261.2 mm, and the temperature was kept at 26.0 °C. The 2D data were integrated into the one-dimensional scattering function I(q), as a function of the magnitude of the scattering vector q defined as Equation (1):
λ is the wavelength and 2θ is the scattering angle. Each measurement was collected for 5 min. All I(q) data were normalized to have the uniform primary intensity at q = 0 for transmission calibration. Desmearing was necessary because of the line collimation.
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7

SAXS Analysis of Lyotropic Liquid Crystals

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SAXS measurements were performed using a SAXSess camera (Anton Parr, Austria) attached to a PW3830 X-ray generator (PANalytical, The Netherlands) , which was operated at 40 kV and 50 mA, with a sealed-tube anode (Cu-Kα wavelength of 0.154 nm) . The measurements were carried out at room temperature. Two-dimensional scattering patterns recorded on an image plate detector were read out by a Cyclone system (Perkin-Elmer, Downers Grove, IL, USA) and were converted into one-dimensional curves as a function of the scattering vector, q= (4π/λ ) sin (θ /2) , where θ is the total scattering angle, with SAXSQuant software (Anton Paar) . All scattering intensities were transmission calibrated by adjusting the attenuated primary intensity at q=0 to unity and corrected for the background scattering of the sample cell and solvent. The SAXS peak ratio was used to confirm the type of the lyotropic liquid crystals.
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8

Small-Angle X-ray Scattering of Starch Gels

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Small-Angle X-ray Scattering (SAXS) measurements were performed on a SAXSess small-angle X-ray scattering system (Anton-Paar, Austria). Samples were measured with a PW3830 X-ray generator (PANalytical) with the X-ray source of Cu Kα radiation (λ = 0.1542 nm). The voltage was set at 40 kV and the current at 50 mA. Each starch gel was filled into a capillary of 1 mm diameter and 0.01 mm wall thickness, and the temperature kept at 25 °C for 10 min with the X-ray exposure. The recorded data in an image plate was collected by the IP Reader software using a PerkinElmer Storage Phosphor System. All collected data were normalized, the background and smeared intensity were subtracted using SAXSquant 2D and SAXSquant 3.0 software was used to further analyze the data ( Chi et al., 2018b) .
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9

SAXS Measurements of Hydrated Samples

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SAXS measurements were performed on a SAXSess small-angle X-ray scattering (SAXS) system (Anton-Paar, Austria) according to our previous methods (Zhang, Chen, Li, Li, & Zhang, 2015; (link)Zhang, Chen, Zhao, & Li, 2013; (link)Zhang, Li, Liu, Xie, & Chen, 2013) (link). Samples were measured at 50 mA and 40 kV using a PW3830 X-ray generator (PANalytical) equipped with an X-ray source of Cu Kα radiation (λ = 0.1542 nm). Each sample with a moisture content of about 60% was prepared and equilibrated at room temperature for 24 h, before being placed into a paste cell and measured for 5 min under X-ray. The data, recorded in an image plate, were collected using the IP Reader software using a PerkinElmer Storage Phosphor System. All collected data were normalized, and the background intensity and smeared intensity were subtracted by using SAXSquant 2D software and SAXSquant 3.0 software, respectively.
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