Process for preparing amino acid chelate compounds, amino acid chelate compounds and use of amino acid chelate compounds
Through the solid-state reaction method of mechanical activation and thermal activation, the complexity and stability problems of amino acid chelate preparation are solved, and efficient and stable amino acid chelate preparation is achieved, which is suitable for industrial applications.
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Embodiment 1
[0073] Experiments with the method according to the invention were carried out in a satellite milling vessel with a volume of 2.7 liters, flange-mounted on an eccentric vibratory mill of the type 656-0.5ks. The grinding chamber of the satellite grinding vessel is ceramic lined to avoid contamination.
[0074] The work described is carried out under the following operating conditions:
[0075] Speed: 960min -1
[0076] Amplitude 12mm
[0077] Grinding body steel
[0078]150 g of copper oxide powder having a particle size 3 In the presence of ions, it is transformed into the known blue tetraamine complex [Cu(NH 3 ) 4 ] -2 . Examination of the crystal structure using an X'Pert X-ray diffractometer from the Philips company showed bis(glycinate)copper (C 4 h 8 CuN 2 o 4 ), which is listed in the ESTM index with the number 00-018-1714.
[0079] The results of X-ray diffractometer measurements are shown in figure 2 middle.
[0080] Particle shape was examined using a s...
Embodiment 2
[0082] Use of the method according to the invention for the production of glycinate salts of copper, zinc, iron, manganese and nickel in terms of CuO, ZnO, FeSO 4 ·H 2 O, MnCO 3 and NiO mixtures are shown. Based on this, 150 g of the mixture described above, in which the components make up 20%, were mechanically activated for 25 minutes in the same research apparatus as in Example 1. The satellite grinder was then opened and 300 g of glycine was added. Next, thermal activation was performed for 5 minutes at an operating temperature of 105°C. The water vapor generated is released through the discharge valve.
[0083] Solubility tests in water at 25°C gave full availability of all metals used after 60 minutes. The aqueous solution was clear and had a slight olive oil mixture color. No X-ray structure pictures were obtained because the lines of the glycinate salts of the metals used overlapped.
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Abstract
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