Yellow organic dye and preparation thereof
A technology of inorganic pigments and yellow pigments, applied in the fields of inorganic pigment processing, inorganic chemistry, chemical instruments and methods, etc., can solve the problems of cost, unsatisfactory color performance in industrial applications, and long time.
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Embodiment 1
[0050] PR 2 MoO 6 Preparation of yellow pigment
[0051] This example involves Pr 2 MoO 6 Pigment preparation. Pr 6 o 11 (purity 99.9%) and (NH 4 ) 6 Mo 7 o 24 4H 2 O (purity 99.9%) was mixed well in an agate mortar and pestle in a stoichiometric ratio. The mixture was calcined at 1050° C. for 9 hours in air. The powder obtained was examined by means of X-ray powder diffraction (XRD) with Ni-filtered CuKα1 radiation with a Philips X'pert Pro diffractometer. figure 1 The XRD pattern of the compound shown in is in good agreement with Powder X-ray Diffraction Archive: PDF No. 24-913. Morphological analysis was performed by means of a scanning electron microscope with a JEOL JSM-5600LV SEM. The particle size of the pigments varies in the range of 1-2 μm. The optical reflectance of the powder measured with a UV-Vis spectrophotometer (Shimadzu, UV-2450) with barium sulfate as a reference is shown in figure 2 middle. The chromaticity coordinate determined by the CIE...
Embodiment 2
[0053] PR 2 MtO 8 Preparation of (Tm=Ti or Zr) Yellow Pigment
[0054] This example describes the Pr 2 MtO 8 Synthesis of (Tm=Ti or Zr). TiO 2 (purity 99.9%), ZrO 2 (purity 99.9%), Pr 6 o 11 (purity 99.9%) and (NH 4 ) 6 Mo 7 o 24 4H 2 O (purity 99.9%) was mixed well in an agate mortar and pestle in a stoichiometric ratio. The mixture was calcined at 1100° C. for 9 hours in air. The powder obtained was examined by means of X-ray powder diffraction (XRD) with Ni-filtered CuKα1 radiation with a Philips X'pert Pro diffractometer. image 3 The XRD pattern of the compound shown in is in good agreement with Powder X-ray Diffraction File: PDF No. 49-0601. Morphological analysis was performed by means of a scanning electron microscope with a JEOL JSM-5600LV SEM. The particle size of the pigment powder was found to vary in the range of 1-5 μm. The optical reflectance of the powder measured with a UV-Vis spectrophotometer (Shimadzu, UV-2450) with barium sulfate as a refe...
Embodiment 3
[0058]A Pr 2 MoO 7 (A=Mg, Ca, Sr or Ba) Preparation of Yellow Pigment
[0059] This example relates to APr 2 MoO 7 Synthesis of (A = Mg, Ca, Sr or Ba). MgCO 3 (purity 99.9%), CaCO 3 (purity 99.9%), SrCO 3 (purity 99.9%), BaCO 3 (purity 99.9%), Pr 6 o 11 (purity 99.9%) and (NH 4 ) 6 Mo 7 o 24 4H 2 O (purity 99.9%) was mixed well in an agate mortar and pestle in a stoichiometric ratio. The mixture was calcined at 950° C. for 6 hours in air. The powder obtained was examined by means of X-ray powder diffraction (XRD) with Ni-filtered CuKα1 radiation with a Philips X'pert Pro diffractometer. The XRD pattern of the compound is shown in Figure 5 middle. This XRD pattern can be compiled into the phases associated with yttrium niobite. Morphological analysis was performed by means of a scanning electron microscope with a JEOL JSM-5600LV SEM. The particle size of the pigments varies in the range of 1-5 μm. The optical reflectance of the powder measured with a UV-Vi...
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