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Carbon Dioxide → Terephthalic Acid

HRID 1979101
ノート
印刷プレビュー

反応式

HRID 1979101 の反応式
C(=O)(O)[O-].[Na+].[C:6]1(=[O:19])[O:16]CC[O:13][C:11](=[O:12])[C:10]2[CH:17]=[CH:18][C:7]1=[CH:8][CH:9]=2.C(=O)=O>O>[C:6]([OH:19])(=[O:16])[C:7]1[CH:18]=[CH:17][C:10]([C:11]([OH:13])=[O:12])=[CH:9][CH:8]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 280Carbon DioxideHCID 516892Sodium BicarbonateHCID 15066111Ethylene terephthalate, cyclic-(1:1)-

生成物 1

HCID 7489Terephthalic Acid

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

反応条件

温度
200 °C

実験手順

In a heated autoclave, provided with a mixer and filled partially with water, cut poly/ethyleneterephtalate/ wastes in a form of scraps of foil and pieces of industrial shapes were placed in the amount of 1000 g together with a solution of 875 g of sodium bicarbonate (NaHCO3) in 10 liters of water, and then a content of the reactor was heated up to 200° C. and the temperature was kept till the digestion of poly/ethylene terephtalate/ was completed and the formation of carbon dioxide was stopped. Then the autoclave was relieved and carbon dioxide and water excess were separated, then a resulted solution was filtered hot through a filter with active carbon. The filtrate was neutralised with hydrochloric acid and a precipitate of terephtalic acid was separated from a reaction solution using a centrifuge. The resulted product was washed with a distilled water and crystallised from water, giving 864 g of terephtalic acid. At the same time ethylene glycol was separated from the neutralised filtrate using extraction with diethylcarbonate, obtaining 322,6 g of ethylene glycol.

後処理

  1. customIn a heated autoclave, provided with a mixer and
  2. customcarbon dioxide and water excess were separated
  3. filtrationa resulted solution was filtered hot through
  4. filtrationa filter with active carbon
  5. customa precipitate of terephtalic acid was separated from a reaction solution
  6. washThe resulted product was washed with a distilled water
  7. customcrystallised from water

出典と根拠

ORDレコード
ord-08165c85cbfe4362af6acdaadf2df849
出典データセット
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06239310B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート