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Formaldehyde → Melamine formaldehyde

HRID 6325
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HRID 6325 반응식
[Na].[N:2]1[C:9]([NH2:10])=[N:8][C:6]([NH2:7])=[N:5][C:3]=1[NH2:4].[CH2:11]=[O:12].[OH-].[Na+]>O>[CH2:11]=[O:12].[N:2]1[C:9]([NH2:10])=[N:8][C:6]([NH2:7])=[N:5][C:3]=1[NH2:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 712FormaldehydeHCID 7955MelamineHCID 14798Sodium HydroxideHCID 5360545Sodium

생성물 1

HCID 93374Melamine formaldehyde

시약·촉매·용매 1

HCID 962Water용매

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온도
60 °C

실험 절차

50 parts of 20% liquor A (dispersion of aromatic isocyanate compound) and 100 parts of 30% liquor B (co-dispersion of imino compound-sensitizer) obtained in the above (1) were mixed with each other until a homogeneous mixture was obtained. 150 parts of the mixture of liquor A and liquor B was gradually added with 120 parts of a 5% aqueous solution of sodium salt of styrene-maleic anhydride copolymer adjusted to pH 4.0 with stirring. Stirring was carried out for about 30 minutes to obtain agglomerates having an average particle diameter of 10 μm and it was simultaneously confirmed that the agglomerates were emulsified and dispersed. Separately, a mixture comprising 11.4 parts of melamine, 28.5 parts of a 37% aqueous formaldehyde solution and 74.1 parts of water was adjusted to pH 9.0 with sodium hydroxide and then was heated at 60° C. with stirring to perform dissolution to obtain 114 parts of a transparent melamine-formaldehyde precondensate.

후처리

  1. additionwere mixed with each other until a homogeneous mixture
  2. customwas obtained
  3. addition150 parts of the mixture of liquor A and liquor B
  4. stirringStirring
  5. customto obtain agglomerates
  6. additiondispersed
  7. stirringwith stirring
  8. dissolutiondissolution

출처 및 근거

ORD 기록
ord-0ff8025e8c5444e9b4b310a7c0c96dda
출처 데이터셋
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05248555

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