Procedure for the anti-scaler production for coating the polymer

Compositions – Water-softening or purifying or scale-inhibiting agents – Packages or heterogeneous arrangements

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252178, 422241, 5253288, 525346, 526 62, 4273882, B01J 1902, B05D 302, B05D 310

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active

060803320

DESCRIPTION:

BRIEF SUMMARY
TECHNICAL FIELD

The object of this invention is a procedure for the anti-scaler production for coating the polymerizing reactors and respective product.
Anti-scaling agents for polymerizing reactors are already well known in prior art.


BACKGROUND ART

At the present state of the art there are also different types of anti-scalers for each type of polymer.
For example the anti-scaler for the production of vinyl chloride is not the same as that used in the reactor for the production of polystyrene or of that for the production of acrylic polymers, and so on.
This fact necessitates the stockage of different products with all the consequences of high management costs.
Additionally even the reactors must be specifically dedicated to only one reaction type, resulting in the increase of costs.


DISCLOSURE OF INVENTION

A first aim of this invention is that to make an anti-scaler that operates well in any type of polymerizing reactor and for the most varied types of different materials, therefore for polystyrene as well as for acrylic polymers, ABS, polybutadiene and PVC, etc.
In the specific case of polymerizing of vinyl chloride in suspension or emulsion for example, it is known that in the reactors a substantial deposit of scale forms having as main drawbacks: interruption of the production, opening of the reactor and therefore high quantities of gaseous vinyl monomer chloride (VCM) emissions into the atmosphere; respective polymerized product with consequent worsening in quality and complaints by the users; problems for the areas in which the industrial polyvinylchloride plants (P.V.C.) operates.
This problem practically exists for all types of polymerizations.
Furthermore the anti-scaling products destined to coat the surfaces of the respective reactors are of a bluish colour or dark brown nearly black, wherefore the particles that detach from the crust, pollute the obtained polymer (for example obtained polyvinyl chloride) from the reactor under the form of black dots, that for example in the finished products worsens the qualitative aspect of the same product.
Furthermore it is to be noted that the material particles that detach from the crust of the wall, end up in the product in reaction, constituting the pollution of the same, dealing generally with toxic products.
In prior art, the technique of condensation or polycondensation of naphthols and phenol with an aldehydic cross-linking product (e.g. formaldehyde and others), to obtain anti-scaling products is known.
For this purpose one refers to:
U.S. Pat. No. 3,669,946 (filed in the U.S. on Aug. 31st, 1970, disclosed on Jun. 13th, 1972), that suggests the use of formaldehyde and ketonic composites, naphthol etc. and also alpha-naphthylamine and nigrosin. This teaching predivulges the general concept of forming condensate anti-scalers parting from the formaldehyde with phenols and naphthols derivatives.
U.S. Pat. No. 3,825,434 (Jul. 23rd 1974) describes an anti-scaling agent for the polymerizing of vinyl chloride, obtained from the condensation of the phenol with formaldehyde, where obviously for definition in this patent the obtained product is always classified as pertinent to the phenol-formaldehyde or polyarylphenol family.
U.S. Pat. No. 4,068,059 (filed on Feb. 17, 1977 published on the Oct. 1, 1978) explains furthermore the importance of using as anti-scalers, products that in their chemical structure contain one or more of the following groups: --OH; --COOH; SO3H and SO3Na. These groups are usually attached to an aromatic nucleus.
EP-A-0052421 describes a process for obtaining an anti-scaling product formed with formaldehyde that is made to react with 1-naphthol (alpha-naphthol), in which both the nuclear positions 2 and 4 are not replaced and the nuclear position 3 is not replaced or has a substitute that is not strongly eletron-attractor to obtain a condensate.
Even in this case the product obtained according to the chemistry is to be considered always as pertinent to the poliarylphenol family.
These last products have the drawback to supply, a

REFERENCES:
patent: 2597281 (1952-05-01), Borstelmann et al.
patent: 3617167 (1971-11-01), Berth et al.
patent: 3669946 (1972-06-01), Koyanagi et al.
patent: 3825434 (1974-07-01), Berens et al.
patent: 4068059 (1978-01-01), Witenhafer
patent: 5424003 (1995-06-01), Shimizu et al.
patent: 5508361 (1996-04-01), Shimizu et al.
patent: 5691428 (1997-11-01), Shimizu et al.
patent: 5888589 (1999-03-01), Carlin et al.
patent: 5965094 (1999-10-01), Sattin
The Merck Index an Encyclopedia of Chemicalc, Drugs and Biologicals, Tenth Edition, (Merck & Co., Inc., Rahway, NJ, copyright 1983) p. 1235, entry 8454, Jan. 1984.

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