Microencapsulated catalyst
A technology of microencapsulation and catalyst, applied in microcapsule preparation, catalyst protection, physical/chemical process catalyst, etc., can solve problems such as the difficulty of catalytic materials, and achieve the effect of reducing deactivation paths, prolonging service life, and being easy to handle.
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Embodiment 1-1
[0086] The encapsulation of embodiment 1-1Kg scale nickel-aluminum alloy
[0087] For a theoretical 1.33 kg batch, the following raw materials are required, which yield approximately 2.8 kg of beads under 50% wet water conditions.
[0088] raw material
the form
weight
volume
Stabilizer Reax TM 100M
840g
n / a
Surfactant Tergitol TM XD 100%
solid
105g
n / a
Surfactant Polyvinyl Alcohol 100%
solid
420g
n / a
Deionized water for aqueous phase
the liquid
n / a
9135ml
Chloroform stabilized with pentene
the liquid
2880g
2009ml
Polymethylpolyphenylisocyanate
the liquid
1350g
1125ml
DispersantSolsperse TM 32000
solid
27.34g
n / a
nickel-aluminum alloy
solid
270g
n / a
deionized water for decantation
the liquid
20000g
20000ml
Deionized water for washing
the liq...
Embodiment 2-250
[0105] Preparation of activated Ni EnCat under the scale of embodiment 2-250g
[0106] 1 L of deionized water was added to a 2 L screw cap jar, followed by 50 g of sodium hydroxide pellets in aliquots every 5 minutes while stirring, for a total of 240 g. Once all the sodium hydroxide had been added, the solution was cooled to room temperature and sparged with nitrogen continuously.
[0107] To a device equipped with a mechanical stirrer, thermocouple, condenser and N 2 Add 400ml of the caustic alkali solution prepared above into the 3L jacketed-flange reactor at the inlet, and inject nitrogen into the reactor. Weigh 200 g of wet water Ni EnCat beads and add to the reactor in 50 g portions while stirring. Rapid bubbling was observed, then the resulting hydrogen was vented through a dehydrator. After 10 minutes, the reaction had subsided, and then another 50 g of beads were added to the reactor. This process was repeated until all beads had been added to the reactor. The re...
Embodiment 3-4
[0110] The reduction of embodiment 3-4-chloronitrobenzene
[0111]
[0112] Activated Ni EnCat (0.26 g, wet water, 20 mol% Ni on substrate) was washed three times with IMS to remove water and added to IMS (4 ml) containing 4-chloronitrobenzene (0.157 g, 1 mmol) solution in a pressure vessel. The vessel was sealed and flushed twice with hydrogen, then pressurized to 5-6 bar with hydrogen and the contents stirred magnetically at room temperature. The progress of the reaction was analyzed by GCMS. After 24 hours, the hydrogen was vented and the Ni EnCat beads were removed by filtration. The filtrate was concentrated on a rotary evaporator to give 4-chloroaniline (0.12 g, 95%). GCMS purity 86%.
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