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Polyvinyl alcohol

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Polyvinyl alcohol
Names
Other names
PVOH; Poly(Ethenol), Ethenol, homopolymer; PVA; Polyviol; Vinol; Alvyl; Alcotex; Covol; Gelvatol; Lemol; Mowiol; Mowiflex, Alcotex, Elvanol, Gelvatol, Lemol, Mowiol, Nelfilcon A, Polyviol und Rhodoviol
Identifiers
ChEMBL
ChemSpider
  • none
ECHA InfoCard 100.121.648 Edit this at Wikidata
E number E1203 (additional chemicals)
KEGG
RTECS number
  • TR8100000
Properties
(C2H4O)x
Density 1.19-1.31 g/cm3
Melting point 200 °C (392 °F; 473 K)
log P 0.26 [1]
1.477 @ 632 nm[2]
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
Flash point 79.44 °C (174.99 °F; 352.59 K)
Lethal dose or concentration (LD, LC):
14,700 mg/kg (Mouse)
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Poly(vinyl alcohol) (PVOH, PVA, or PVAl) is a water-soluble synthetic polymer. It has the idealized formula [CH2CH(OH)]n. It is used in papermaking, textiles, and a variety of coatings. It is white (colourless) and odorless. It is sometimes supplied as beads or as solutions in water.[3]

Uses

Polyvinyl alcohol is used as an emulsion polymerization aid, as protective colloid, to make polyvinyl acetate dispersions. This is the largest market application in China. In Japan its major use is vinylon fiber production.[4]

Other uses of polyvinyl alcohol include[citation needed] injection moulding of soluble containers for active release of detergents and agrichemicals, paper adhesive with boric acid in spiral tube winding and solid board production, thickener, modifier, in polyvinyl acetate glues, textile sizing agent, Paper coatings, release liner, as a water-soluble film useful for packaging (an example is the envelope containing laundry detergent in "liqui-tabs"), feminine hygiene and adult incontinence products as a biodegradable plastic backing sheet, carbon dioxide barrier in polyethylene terephthalate (PET) bottles, as a film used in the water transfer printing process, as a form release because materials such as epoxy do not stick to it, movie practical effect and children's play putty or slime when combined with borax, used in eye drops (such as artificial tears to treat dry eyes) and hard contact lens solution as a lubricant, PVA fiber as reinforcement in concrete, raw material to polyvinyl nitrate (PVN) an ester of nitric acid and polyvinyl alcohol, as a surfactant for the formation of polymer encapsulated nanobeads, used in protective chemical-resistant gloves, used as a fixative for specimen collection, especially stool samples, when doped with iodine, PVA can be used to polarize light, as an embolization agent in medical procedures, carotid phantoms for use as synthetic vessels in Doppler flow testing, and used[citation needed] in 3D printing as support structure that can then be dissolved away (cire perdue).

Polyvinyl acetals

Polyvinyl acetals are prepared by reacting aldehydes with polyvinyl alcohol. Polyvinyl butyral (PVB) and polyvinyl formal (PVF) are examples of this family of polymers. They are prepared from polyvinyl alcohol by reaction with butyraldehyde and formaldehyde, respectively. Preparation of polyvinyl butyral is the largest use for polyvinyl alcohol in the U.S. and Western Europe.

Fishing

PVA is widely used in freshwater sport fishing.[citation needed] PVA moulded capsules and small bags made from PVA are filled with dry or oil based bait and attached to the hook, or the baited hook is placed inside the bag and cast into the water. When the bag lands on the lake or river bottom it dissolves in water, leaving the hook bait surrounded by ground bait, pellets etc.

Anglers also use string made of PVA for the purpose of making temporary attachments. For example, holding a length of line in a coil, that might otherwise tangle while the cast is made.

Preparation

Unlike most vinyl polymers, PVA is not prepared by polymerization of the corresponding monomer. The monomer, vinyl alcohol, is unstable with respect to acetaldehyde. PVA instead is prepared by first polymerizing vinyl acetate, and the resulting polyvinylacetate is converted to the PVA.[3] Other precursor polymers are sometimes used, with formate, chloroacetate groups instead of acetate. The conversion of the polyesters is usually conducted by base-catalysed transesterification with ethanol:

The properties of the polymer depend on the amount of residual ester groups.

Worldwide consumption of polyvinyl alcohol was over one million metric tons in 2006.[4] Larger producers include Kuraray (Japan, Europe, and USA) and Sekisui Specialty Chemicals (USA) but mainland China has installed a number of very large production facilities in the past decade and currently accounts for 45% of world capacity. The North Korean-manufacture fiber Vinalon is produced from polyvinyl alcohol. Despite its inferior properties as a clothing fiber, it is produced for self-sufficiency reasons, because no oil is required to produce it.

Structure and properties

PVA is an atactic material that exhibits crystallinity. In terms of microstructure, it is composed mainly of 1,3-diol linkages [-CH2-CH(OH)-CH2-CH(OH)-] but a few percent of 1,2-diols [-CH2-CH(OH)-CH(OH)-CH2-] occur, depending on the conditions for the polymerization of the vinyl ester precursor.[3]

Polyvinyl alcohol has excellent film forming, emulsifying and adhesive properties. It is also resistant to oil, grease and solvents. It has high tensile strength and flexibility, as well as high oxygen and aroma barrier properties. However these properties are dependent on humidity, in other words, with higher humidity more water is absorbed. The water, which acts as a plasticiser, will then reduce its tensile strength, but increase its elongation and tear strength.

PVA has a melting point of 230 °C and 180–190 °C (356-374 degrees Fahrenheit) for the fully hydrolysed and partially hydrolysed grades, respectively. It decomposes rapidly above 200 °C as it can undergo pyrolysis at high temperatures.

PVA is close to incompressible. The Poisson's ratio is between 0.42 and 0.48.[5]

Tradenames of polyvinyl alcohol

Tradenames include Gohsenol, Kuraray Poval, Mowiol, Selvol, Exceval, Polyviol, Sinopac, and Elvanol.[citation needed]

Safety

PVA is nontoxic. It biodegrades slowly, and solutions containing up to 5% PVA are nontoxic to fish.[3]

See also

References

  1. ^ "Poly(vinyl alcohol)_msds".
  2. ^ Schnepf, M.J.; Mayer, M.; Kuttner, C.; Tebbe, M.; Wolf, D.; Dulle, M.; Altantzis, T.; Formanek, P.; Förster, S.; Bals, S.; König, T.A.F.; Fery, A. (2017). "Nanorattles with tailored electric field enhancement". Nanoscale. 9 (27): 9376–9385. doi:10.1039/C7NR02952G.
  3. ^ a b c d Manfred L. Hallensleben "Polyvinyl Compounds, Others" in Ullmann's Encyclopedia of Industrial Chemistry, 2000, Wiley-VCH, Weinheim. doi:10.1002/14356007.a21_743
  4. ^ a b SRI Consulting CEH Report Polyvinyl Alcohol, published March 2007, abstract retrieved July 30, 2008.
  5. ^ Characterization of PVA cryogel for intravascular ultrasound elasticity imaging, Fromageau, J.; Brusseau, E.; Vray, D.; Gimenez, G.; Delachartre, P.; IEEE Transactions on Ultrasonics, Ferroelectrics and Frequency Control, Volume: 50, Issue: 10. 2003, Page(s): 1318 - 1324.

External links


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