X-Ray Diffraction (XRD) is a non-destructive technique for the qualitative and quantitative analysis of the crystalline materials, in form of powder or solid.
GNR has developed, in cooperation with academic and industrial users, a set of technically advanced and flexible diffractometers able to satisfy different level of requirements and different operating budget.
GNR XRD Product Portfolio covers a huge range of applications for materials characterization and quality control of crystalline or non-crystalline materials such as powders, specimens, thin films or liquids.
Basically XRD is obtained as the „reflection“ of an X-ray beam from a family of parallel and equally spaced atomic planes, following the Bragg’s law: when a monochromatic X-ray beam with wavelength l is incident on lattice planes with an angle q, diffraction occurs if the path of rays reflected by successive planes (with distance d) is a multiple of the wavelength.
Qualitative analysis (phase analysis) can be done thanks to the comparison of the diffractogram obtained from the specimen with a huge number of patterns included in the official databases. Single phases and/or mixtures of phases can be analysed with the programs available today.
Many Investigations can be performed with the help of X-ray diffraction.
Residual Stress Forces that results in a small compression or dilatation of the d-spacing. With XRD it is possible to measure the strain (the deformation of the original lattice) and the stress is calculated thanks to the knowledge of the elastic constants of the material
Texture It is the preferred orientation of the crystallites in a specimen. If a texture in a material is present, the intensity of a diffraction line changes with the orientation of the sample respect to the incident beam.
Crystallite size and micro strain These information are obtained by the analysis of the width and the shape of the diffraction lines.
Structure analysis XRD is used to investigate the crystallographic structure of a material. The position and the relative intensities of the diffraction lines can be correlated to the position of the atoms in the unit cell, and its dimensions. Indexing, structure refinement and simulation can be obtained with specific computer programs.
Thin film Keeping the incident beam at low angles, it is possible to investigate the properties of multilayers, minimising the interference of the substrate. On the same way, reflectometry can be performed.
APD 2000 PRO diffractometer is an high power – Theta/2Theta – laboratory powder X-Ray Diffractometer equipped with all the most moder technical features which grant accuracy, precision, safety and easiness of use for XRD analysis of polycrystalline materials.
Thanks to a wide offer of configurations and accessories such as high-speed detector, scintillation counter, high-low temperature and humiduty chamber, secondary monochromator, spinner and multiple sample holder, APD 2000 PRO is a powerful tool for powder diffraction applications such as routinary qualitative and quantitative phase analysis, non-ambient analysis, structure solution and refinement, crystallite size and degree of crystallinity calculation.
APD 2000 PRO Key Features
Applications:
Qualitative and quantitative phase analysis, non-ambient analysis, retained austenite quantification, structure solution and refinement, crystallite size and crystallinity calculations.
X Ray Generator | Maximum Output Power | 3 kW (option: 4 kW) |
Output Stability | < 0.01 % (for 10% power supply fluctuation) | |
Max Output Voltage | 60 kV | |
Max Output Current | 60 mA (option: 80 mA) | |
Voltage Step Width | 0.1 kV | |
Current Step Width | 0.1 mA | |
Ripple | 0.03% rms < 1kHz, 0.75% rms > 1kHz | |
Preheat and Ramp | Automatic preheat and ramp control circuit | |
Input Voltage | 220 Vac +/-10%, 50 or 60 Hz, single phase | |
Size | Width 48.3 cm, height 13.3 cm, depth 56 cm | |
X-Ray Tube | Type | Glass (option: Ceramic), Cu Anode, Fine Focus (options: any kind of X-Ray tube) |
Focus | 0.4 x 12 mm LFF (other options available) | |
Max Output | 3.0 kW | |
Goniometer | Configurations | Vertical and Horizontal Theta/2Theta geometry |
Measuring circle diameters | 350 – 400 mm | |
Vertical Scanning Angular Range | – 60° < 2 Theta < + 168° (according to accessories) | |
Horizontal Scanning Angular Range | – 110° < 2 Theta < + 168° (according to accessories) | |
Smallest selectable stepsize | 0.0001° | |
Angular reproducibility | +/- 0.0001° | |
Modes of operation | Continuous scan, step scan, theta or 2 theta scan, fast scan, theta axis oscillation | |
Variable Divergence slits | 0 – 4° | |
Variable Anti-Divergence slits | 0 – 4° | |
Variable Receiver slits | 0 – 4° | |
Soller slits | 2° | |
Detector | Type | Scintillation counter Nal (options: YAP(Ce); multistrip) |
Countrate | 2 x 10(6) cps (Nal); 2 x 10(7) cps (Yap(Ce)) | |
Case | Dimensions | Width 850 mm, heigh 1680 mm, depth 750 mm |
Leakage X-rays | < 1 mSv/Year (full safety shielding according to the international guidelines) | |
Processing Unit | Computer Type | Personal Computer, the latest version |
Items controlled | X-ray generator, goniometer, sample holder, detector, counting chain | |
Basic Data Processing | Polynomial least squares smoothing. Fourier smoothing. Search for Peaks (automatic and manual). Spline background subtraction. Single peak analysis (area, FWHM, centroid, background). Marquardt fit (with pseudo-Voigt and Pearson VII curves, Ka2 contribution, weighted sum of squares). Sum and multiply by a constant. Scale normalization. Zoom. Graphical windows. Overlap and comparison of diffractograms. Multiview function. Cursor scan. Creation of graphic files .BMP. ICDD-PDF2 Card Overlap. Creation of calibration curves. Analysis of unknown samples. Qualitative and quantitative phase analysis. Rietveld analysis, crystalline structural analysis, crystallite size and lattice strain, crystallinity calculation |
Data Collection Programs
GNR offers a large variety of acquisition programs, for standard as well as for customized hardware configurations. the list includes programs for powder and high resolution diffractometers, retained austenite, data acquisition of stress (plane and triaxial) and thin films (XRD and GIXRD).
SAX
Single peak analysis; peak treatment. Background subtraction, smoothing, deconvolution and peak localisation. Structural Analysis, Crystallite Size, Lattice Strain, Reflectometry, Quantitative Analysis.
Search and Match: MATCH!
Rietveld refinement, Display and compare multiple diffraction partners, Directly view specific phases/entries, instant usage of additional information, saving of selection criteria, Comfortable definition of background, Improved zooming facilities, Batch processing and Automatics.
Applications
Qualitative and quantitative phase analysis, non-ambient analysis, retained austenite quantification, structure solution and refinement, crystallite size and crystallinity calculations.
X-Ray Diffraction (XRD) is a non-destructive technique for the qualitative and quantitative analysis of the crystalline materials, in form of powder or solid.
GNR has developed, in cooperation with academic and industrial users, a set of technically advanced and flexible diffractometers able to satisfy different level of requirements and different operating budget.
GNR XRD Product Portfolio covers a huge range of applications for materials characterization and quality control of crystalline or non-crystalline materials such as powders, specimens, thin films or liquids.
Basically XRD is obtained as the „reflection“ of an X-ray beam from a family of parallel and equally spaced atomic planes, following the Bragg’s law: when a monochromatic X-ray beam with wavelength l is incident on lattice planes with an angle q, diffraction occurs if the path of rays reflected by successive planes (with distance d) is a multiple of the wavelength.
Qualitative analysis (phase analysis) can be done thanks to the comparison of the diffractogram obtained from the specimen with a huge number of patterns included in the official databases. Single phases and/or mixtures of phases can be analysed with the programs available today.
Many Investigations can be performed with the help of X-ray diffraction.
Residual Stress Forces that results in a small compression or dilatation of the d-spacing. With XRD it is possible to measure the strain (the deformation of the original lattice) and the stress is calculated thanks to the knowledge of the elastic constants of the material
Texture It is the preferred orientation of the crystallites in a specimen. If a texture in a material is present, the intensity of a diffraction line changes with the orientation of the sample respect to the incident beam.
Crystallite size and micro strain These information are obtained by the analysis of the width and the shape of the diffraction lines.
Structure analysis XRD is used to investigate the crystallographic structure of a material. The position and the relative intensities of the diffraction lines can be correlated to the position of the atoms in the unit cell, and its dimensions. Indexing, structure refinement and simulation can be obtained with specific computer programs.
Thin film Keeping the incident beam at low angles, it is possible to investigate the properties of multilayers, minimising the interference of the substrate. On the same way, reflectometry can be performed.
APD 2000 PRO diffractometer is an high power – Theta/2Theta – laboratory powder X-Ray Diffractometer equipped with all the most moder technical features which grant accuracy, precision, safety and easiness of use for XRD analysis of polycrystalline materials.
Thanks to a wide offer of configurations and accessories such as high-speed detector, scintillation counter, high-low temperature and humiduty chamber, secondary monochromator, spinner and multiple sample holder, APD 2000 PRO is a powerful tool for powder diffraction applications such as routinary qualitative and quantitative phase analysis, non-ambient analysis, structure solution and refinement, crystallite size and degree of crystallinity calculation.
APD 2000 PRO Key Features
Applications:
Qualitative and quantitative phase analysis, non-ambient analysis, retained austenite quantification, structure solution and refinement, crystallite size and crystallinity calculations.
X Ray Generator | Maximum Output Power | 3 kW (option: 4 kW) |
Output Stability | < 0.01 % (for 10% power supply fluctuation) | |
Max Output Voltage | 60 kV | |
Max Output Current | 60 mA (option: 80 mA) | |
Voltage Step Width | 0.1 kV | |
Current Step Width | 0.1 mA | |
Ripple | 0.03% rms < 1kHz, 0.75% rms > 1kHz | |
Preheat and Ramp | Automatic preheat and ramp control circuit | |
Input Voltage | 220 Vac +/-10%, 50 or 60 Hz, single phase | |
Size | Width 48.3 cm, height 13.3 cm, depth 56 cm | |
X-Ray Tube | Type | Glass (option: Ceramic), Cu Anode, Fine Focus (options: any kind of X-Ray tube) |
Focus | 0.4 x 12 mm LFF (other options available) | |
Max Output | 3.0 kW | |
Goniometer | Configurations | Vertical and Horizontal Theta/2Theta geometry |
Measuring circle diameters | 350 – 400 mm | |
Vertical Scanning Angular Range | – 60° < 2 Theta < + 168° (according to accessories) | |
Horizontal Scanning Angular Range | – 110° < 2 Theta < + 168° (according to accessories) | |
Smallest selectable stepsize | 0.0001° | |
Angular reproducibility | +/- 0.0001° | |
Modes of operation | Continuous scan, step scan, theta or 2 theta scan, fast scan, theta axis oscillation | |
Variable Divergence slits | 0 – 4° | |
Variable Anti-Divergence slits | 0 – 4° | |
Variable Receiver slits | 0 – 4° | |
Soller slits | 2° | |
Detector | Type | Scintillation counter Nal (options: YAP(Ce); multistrip) |
Countrate | 2 x 10(6) cps (Nal); 2 x 10(7) cps (Yap(Ce)) | |
Case | Dimensions | Width 850 mm, heigh 1680 mm, depth 750 mm |
Leakage X-rays | < 1 mSv/Year (full safety shielding according to the international guidelines) | |
Processing Unit | Computer Type | Personal Computer, the latest version |
Items controlled | X-ray generator, goniometer, sample holder, detector, counting chain | |
Basic Data Processing | Polynomial least squares smoothing. Fourier smoothing. Search for Peaks (automatic and manual). Spline background subtraction. Single peak analysis (area, FWHM, centroid, background). Marquardt fit (with pseudo-Voigt and Pearson VII curves, Ka2 contribution, weighted sum of squares). Sum and multiply by a constant. Scale normalization. Zoom. Graphical windows. Overlap and comparison of diffractograms. Multiview function. Cursor scan. Creation of graphic files .BMP. ICDD-PDF2 Card Overlap. Creation of calibration curves. Analysis of unknown samples. Qualitative and quantitative phase analysis. Rietveld analysis, crystalline structural analysis, crystallite size and lattice strain, crystallinity calculation |
Data Collection Programs
GNR offers a large variety of acquisition programs, for standard as well as for customized hardware configurations. the list includes programs for powder and high resolution diffractometers, retained austenite, data acquisition of stress (plane and triaxial) and thin films (XRD and GIXRD).
SAX
Single peak analysis; peak treatment. Background subtraction, smoothing, deconvolution and peak localisation. Structural Analysis, Crystallite Size, Lattice Strain, Reflectometry, Quantitative Analysis.
Search and Match: MATCH!
Rietveld refinement, Display and compare multiple diffraction partners, Directly view specific phases/entries, instant usage of additional information, saving of selection criteria, Comfortable definition of background, Improved zooming facilities, Batch processing and Automatics.
Applications
Qualitative and quantitative phase analysis, non-ambient analysis, retained austenite quantification, structure solution and refinement, crystallite size and crystallinity calculations.
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