Catalyst precursor particles, their preparation and use
A catalyst and precursor technology, applied in the field of silicon oxide particles and its preparation, can solve complex smoke treatment equipment, toxic smoke, harmful and other problems, and achieve the effect of eliminating processing defects
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Embodiment 1
[0075] Example 1 (comparative - organometallic from heptane - homopolymerization - 700°C)
[0076] 100 g of silica xerogel support (pure silica) was prepared by evaporative drying of the hydrosol. The surface area and pore volume of the support were determined by nitrogen porosimetry as described above using a Micromeritics ASAP 2420 analyzer and were 381 m 2 / g and 1.76cm 3 / g.
[0077] Using the Malvern Mastersizer TM The particle size distribution of the carrier particles was determined as follows: d 90 169.3 μm, d 50 is 114.6μm, and d 10 is 63.4 μm. (d 90 90% by weight of the particles have a particle size smaller than d 90 The particle size-equivalent definition applies to d 50 and d 10 ).
[0078] 100 g of silica xerogel support (previously dried at 140° C.) was added to a dry reaction flask equipped with a stirrer. will be 600cm 3 Add heptane to the flask to form a silica / heptane slurry. Add 6.78 g of chromium acetylacetonate to another clean and dry flask...
Embodiment 2
[0080] Embodiment 2 (according to the present invention-homopolymerization-700 ℃)
[0081] A methanolic solution of chromium acetate and aluminum acetate was prepared by adding 1.15 g of chromium acetate and 2.84 g of boric acid stabilized basic aluminum acetate to a beaker equipped with a magnetic stirrer.
[0082] Add about 50cm 3 methanol, and the mixture was stirred for 1 hour to completely dissolve the chromium and aluminum salts. This chrome-aluminum solution was added to 30 g of the dried silica xerogel support used in Example 1, thereby impregnating chromium and aluminum onto the support. Methanol was removed from the resulting catalyst precursor by drying in a vacuum oven at 140° C. for 3 hours. A blue / green catalyst precursor powder was obtained, and the contents of chromium and aluminum were 0.93% by weight and 1.87% by weight, respectively, based on the elements. The boron content was determined to be 1720 ppm by weight. The surface area and pore volume were de...
Embodiment 3
[0085] Example 3 (comparison-impregnating aluminum after impregnating chromium first-homopolymerization-700°C)
[0086] By using 2201cm 3 The aqueous solution of chromium acetate was prepared by diluting the chromium acetate solution containing 7.68 weight% of chromium with the water. This solution was added to 1500 g of the silica xerogel described in Example 1. After dehydration, a fluffy catalyst with a chromium content of 0.97% by weight was obtained. The surface area and pore volume are 380 m 2 / g and 1.62cm 3 / g (ASAP 2420).
[0087] 70 g of this chromium-containing silicon oxide was previously dried at 140° C. for 4 hours, and placed in a closed flask. add 250cm 3 of heptane. Under a nitrogen purge, add 43 cm 3 A 1.0 molar solution of triisobutylaluminum in heptane. After stirring for 30 minutes, the mixture was filtered and the obtained filter cake was dried in a vacuum oven at 140°C. A light blue / green catalyst precursor powder was produced, and the chromium...
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