PARAFORMALDEHYDE

HCID 178665535CAS 25231-38-3

Grundinformationen

Standard-SMILES
CC(=O)OCOC(C)=O
InChIKey
BPGDAMSIGCZZLK-UHFFFAOYSA-N
Summenformel
C3H6O3X2
Durchschnittliche Molmasse
90,08 g/mol

Namen und Bezeichner

Bevorzugter Name
PARAFORMALDEHYDE
Englischer Name
PARAFORMALDEHYDE
Summenformel
C3H6O3X2
Molmasse
90.08

Namen und Synonyme

POLYFORMALDEHYDEPOLYACETALPARAFORMACETAL RESINPOLY(TRIOXANE)POLYOXMETHYLENEPOLYACETAL RESINFORMALDEHYDE RESINPolyoxymethylenediacetateoxymethylene homopolymer diacetate

Datenbank-Bezeichner

CAS
25231-38-3

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
175 °C · 175 °C
Dichte
1.42 g/mL · 1.42 g/mL at 25 °C
Dampfdichte
1.03 · 1.03 (vs air)
Dampfdruck
1.45 mm · <1.45 mm Hg ( 25 °C)
Flammpunkt
158 °F · 158 °F
Löslichkeit
70 °C: · chlorophenol above 70°C: soluble

Sicherheit und Regulatorisches

Sicherheitsdaten

wgk
3
tsca
TSCA listed
ridadr
UN 2213 4.1/PG 3
RTECS-Nr.
RV0540000
risk_code
31
hazard_code
Xn

Chemie und Industrie

Darstellung · 1 Eintrag

synthetische(a) Homopolymers In the preparation of high molecular weight polyformaldehyde the initial operation consists of the production of pure formaldehyde, free from low molecular weight polymers and other hydroxy compounds which cause chain transfer. In a typical process potassium hydroxide-precipitated paraformaldehyde (degree of polymerization approximately 200) is carefully washed with water and dried for several hours in vacuo at 80C. The dried polymer is then decomposed in nitrogen at 150-160C; the product is passed through several traps at -15C to remove water, glycols, and other impurities. The resulting formaldehyde has a water content (free and combined) of less than 0.1 %.The formaldehyde is then introduced into a reactor where it passes over the surface of a rapidly stirred solution of initiator (either a Lewis acid or base; triphenylphosphine appears to be favoured) in a carefully dried inert medium such as heptane at about 40C. The process is designed to give a very low concentration of formaldehyde to minimize transfer from polymer to monomer. To the initiator solution may be added a polymer stabilizer (e.g. diphenylamine) and transfer agents (e.g. traces of water or methanol). Polymerization is continued until the concentration of polymer in the slurry is about 20% and then the polymer is collected by filtration.In the final stage the polymer is subjected to an esterification reaction to improve its thermal stability. The esterification may be effected with a number of anhydrides, but acetic anhydride is generally preferred. Typically, the polyformaldehyde is heated under slight pressure to about 160C with acetic anhydride and a small amount of sodium acetate (catalyst). The polymer is soluble in acetic anhydride at this temperature but is precipitated when the solution is cooled. The acetylated polymer is collected by filtration, washed with water (to remove the anhydride and catalyst) and then acetone (containing di-fi-naphthyl-p-phenylenediamine as antioxidant), and dried in vacuo at 70C. The product is then extruded and chopped into granules. The average molecular weight (Mn) of the polyformaldehyde produced by these methods is generally in the range 30000-100000.The polymerization of formaldehyde by Lewis bases such as triaryl amines (R3N), arsines, and phosphines proceeds by the following anionic mechanism:The polymerization of formaldehyde by Lewis acids such as boron trifluoride proceeds according to following cationic mechanism:The hydroxy-terminated polymers have poor thermal stability. Loss of a proton, possibly to an initiator residue, from a chain end gives an anion capable of decomposing to formaldehyde by the

Anbieter9 Anbieter

上海赛可锐生物科技有限公司021-58000709 13120558703 · [email protected]
上海维亦特生物科技有限公司15317051735 · [email protected]
广东元丰化学试剂有限公司0751-2829979 13376591640 · [email protected]
广东翁江化学试剂有限公司0751-2815987 13927875076 · [email protected]
陕西缔都医药化工有限公司029-029-81120477 17792793610 · [email protected]

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