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POLY(VINYL ACETATE)/PVACCAS NO.: 9003-20-7 CAS NO.9003-20-7
- FOB Price: USD: 4.00-5.00 /Gram Get Latest Price
- Min.Order: 1 Gram
- Payment Terms: L/C,D/A,D/P,T/T,Other
- Available Specifications:
top grade (1-10)Gramtop grade (10-100)Gram
- Product Details
Keywords
- POLY(VINYL ACETATE)
- high purity POLY(VINYL ACETATE)
- 99.5% POLY(VINYL ACETATE)
Quick Details
- ProName: POLY(VINYL ACETATE)/PVACCAS NO.: 9003-...
- CasNo: 9003-20-7
- Molecular Formula: C4H6O2
- Appearance: White solid
- Application: Adhesive and Sealant
- DeliveryTime: in stock
- PackAge: Aluminium foil bag
- Port: China main port
- ProductionCapacity: 10000 Gram/Day
- Purity: 99%
- Storage: Room temperature
- Transportation: By Sea/Air/DHL
- LimitNum: 1 Gram
- first class: 1-10
Superiority
We are leading fine chemicals supplier in China and
Our main business covers the fields below:
1.Noble Metal Catalysts (Pt.Pd...)
2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)
3.OLED intermediates (Fluorene,Carbazole,Boric acid...)
4.Customs Synthesis
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1.Higest quality and good package
2.Fast delivery
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4.Fast response to customer within 6 hours
5.Good business credit in Europe ,US ,Japan ,Korea
Anyway ,if you need any chemicals from China ,Henan Wentao can help you
Details
| Chemical Properties | transparent pellets or white powder |
| Chemical Properties |
The degree of polymerization of polyvinyl acetate typically is 100 to 5000. The ester groups of the polyvinyl acetate are sensitive to base hydrolysis and will slowly convert PVAc into polyvinyl alcohol and acetic acid. Under alkaline conditions, boron compounds such as boric acid or borax cause the polymer to cross-link, forming tackifying precipitates or slime. |
| History |
Polyvinyl acetate was discovered in Germany in 1912 by Fritz Klatte. The monomer, vinyl acetate, was first produced on an industrial scale by addition of acetic acid to acetylene with a mercury(I) salt[3] but it is now primarily made by palladium catalyzed oxidative addition of acetic acid to ethylene. |
| Uses |
As an emulsion in water, aPVAc emulsions are used as adhesives for porous materials, particularly for wood, paper, and cloth, and as a consolidant for porous building stone, in particular sandstone . Uses : As wood glue PVAc is known as "white glue" and the yellow "carpenter's glue" or PVA glue. As paper adhesive during paper packaging converting In bookbinding and book arts, due to its flexible strong bond and non-acidic nature (unlike many other polymers). The use of PVAC on the Archimedes Palimpsest during the 20th century greatly hindered the task of disbinding the book and preserving and imaging the pages in the early 21st century, in part because the glue was stronger than the parchment it held together. The stiff homopolymer PVAc, but mostly the more soft copolymer a combination of vinyl acetate and ethylene, vinyl acetate ethylene (VAE), is used also in paper coatings, paint and other industrial coatings, as binder in nonwovens in glass fibers. sanitary napkins, filter paper and in textile finishing PVAc can also be used as coating to protect cheese from fungi and humidity. Polyvinyl acetate is also the raw material to make other polymers like : Polyvinyl alcohol -[HOCHCH2]-: Polyvinyl acetate is partially or completely hydrolysed to give polyvinyl alcohol. This reversible saponification and esterification reaction was a strong hint for Hermann Staudinger in the formulation of his theory of macro molecules. Polyvinyl acetate phthalate (PVAP): Polyvinyl acetate is partially hydrolyzed and then esterified with phthalic acid. |
| Uses | drug delivery, hemodynamics, wound dressing, coatings |
| Definition | ChEBI: A polymer composed of repeating acetoxyethylene units. |
| Preparation | PVAc is a vinyl polymer. Polyvinyl acetate is prepared by polymerization of vinyl acetate monomer (free radical vinyl polymerization of the monomer vinyl acetate). |
| Production Methods | Polyvinyl acetate is derived from the polymerization of vinyl acetate; the catalysts used in polymerization may include hydrogen peroxide, peroxy sulfates, or various redox combinations. The polymerization process is described as being carried out by charging all ingredients to the reactor, heating to reflux, and stirring until the reaction is complete. Typically, only a part of the monomer and catalyst is initially charged; the remainder is added during the course of the reaction. |
| Hazard | Questionable carcinogen. |
| Industrial uses |
Polyvinyl acetate is a leathery, colorless thermoplasticmaterial that softens at relatively lowtemperatures and that is relatively stable to lightand oxygen. The polymers are clear and noncrystalline.The chief applications of polyvinylacetate are as adhesives and binders for waterbasedor emulsion paints. Vinyl acetate is conveniently prepared bythe reaction of acetylene with acetic acid. |
| Safety Profile | Very low toxicity by ingestion. Questionable carcinogen. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS |
| Purification Methods | Precipitate it from acetone by addition of n-hexane. |