Dicumyl peroxide → Maleic anhydride iminodiacetic acid

HRID 325054

反応式

HRID 325054 の反応式
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[NH:8]([CH2:13][C:14]([OH:16])=[O:15])[CH2:9][C:10]([OH:12])=[O:11].C(OOC(C1C=CC=CC=1)(C)C)(C1C=CC=CC=1)(C)C>>[C:4]1(=[O:5])[O:6][C:1](=[O:7])[CH:2]=[CH:3]1.[NH:8]([CH2:13][C:14]([OH:16])=[O:15])[CH2:9][C:10]([OH:12])=[O:11]

参加物

5

反応物 4

HCID 6641Dicumyl peroxideHCID 7923Maleic AnhydrideHCID 8897Iminodiacetic acidHCID 178435160HCID 178435160、化合物3 回

生成物 1

HCID 18673270Maleic anhydride iminodiacetic acid

反応条件

温度
165 °C

実験手順

A modified polyethylene is made in accordance with the practice of the present invention by initially preheating 42 parts of low density polyethylene to a temperature of 110° C. The polyethylene was agitated for a period of about 5 minutes and a mixture of 1 part of the adduct of maleic anhydride and iminodiacetic acid and 0.042 part of dicumyl peroxide was added to the polyethylene while it was stirred. After the mixture was agitated for two minutes, the temperature of the mixture was raised to 165° C. The resulting melt was then agitated for an additional 10 minutes and then the molten polyethylene was removed. Based on method of preparation, there was obtained maleic anhydride-iminodiacetic acid modified polyethylene. The identity of the product is confirmed by its infrared spectrum and oxygen analysis.

後処理

  1. customto a temperature of 110° C
  2. stirringAfter the mixture was agitated for two minutes
  3. stirringThe resulting melt was then agitated for an additional 10 minutes
  4. customthe molten polyethylene was removed
  5. customBased on method of preparation

出典と根拠

ORDレコード
ord-36c19c8461924846a9fb34aba8ab4813
出典データセット
uspto-grants-2001_04
特許番号
US06221967B1

関連ノート

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