Method and apparatus for producing dicyanobenzene
US-9822062-B2 · Nov 21, 2017 · US
US9878979B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9878979-B2 |
| Application number | US-201615361223-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 25, 2016 |
| Priority date | Nov 30, 2015 |
| Publication date | Jan 30, 2018 |
| Grant date | Jan 30, 2018 |
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The present invention relates to the fine purification of isophoronenitrile (IPN) by melt crystallization.
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The invention claimed is: 1. Process for purifying isophoronenitrile from the production of isophoronenitrile from isophorone and hydrocyanic acid in the presence of a catalyst, characterized in that the removal of impurities in the isophoronenitrile is effected by melt crystallization. 2. Process for purifying isophoronenitrile according to claim 1 , wherein the melt crystallization is effected by suspension crystallization or by layer crystallization. 3. Process for purifying isophoronenitrile according to claim 1 , wherein the melt crystallization is carried out as a layer crystallization in static operation or in dynamic operation or a combination of both process steps. 4. Process for purifying isophoronenitrile according to claim 1 , wherein the melt crystallization is carried out in one stage or in a plurality of stages. 5. Process for purifying isophoronenitrile according to claim 1 , wherein the melt crystallization is carried out in a plurality of stages and wherein the discharged mother liquor and the sweated fraction and also the crystallizate are collected in different buffering containers. 6. Process for purifying isophoronenitrile according to claim 1 , wherein the dynamic melt crystallization is carried out in at least one falling film crystallizer. 7. Process for purifying isophoronenitrile according to claim 1 , wherein the static melt crystallization is carried out in at least one falling film crystallizer or in an at least one plate crystallizer. 8. Process for purifying isophoronenitrile by melt crystallization according to claim 1 , wherein the product mixture composed essentially of isophoronenitrile, the unconverted reactants hydrogen cyanide and isophorone and also the catalyst, methanol and residues is purified as follows: I. purification of the product mixture by a distillation by 1. removal of water, low boilers and methanol and also at least 85% of the isophorone at the top of the column, the isophorone proportion being condensed by means of a partial condenser and recycled into the reaction, 2. removal in the bottom of the column of isophoronenitrile and the remaining isophorone and impurities (high boilers); II. the mixture from I.2. accumulating in the column-bottom is sent to a melt crystallization to remove the impurities and isolate the isophoronenitrile. 9. Process for purifying isophoronenitrile by melt crystallization according to claim 1 , wherein the product stream from the reaction reactor for producing isophoronenitrile composed essentially of isophorone, hydrocyanic acid and catalyst, crude isophoronenitrile, is purified as follows: I. purification of the product stream by a first distillation a) to remove water, low boilers, methanol and some, preferably not more than 10%, of the isophorone at the top of the column, and b) removal in the bottom of the column of isophoronenitrile and the remaining isophorone and impurities (high boilers); II. purification of the product stream from I. b) in a second distillation column and removal of the isophoronenitrile, isophorone and impurities from the bottom of the column; III. the mixture from II accumulating in the column-bottom is sent to a melt crystallization to remove the impurities and isolate the isophoronenitrile.
Separation; Purification · CPC title
The ring being saturated · CPC title
to compounds containing carbon-to-carbon double bonds · CPC title
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