Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Mixing of two or more solid polymers; mixing of solid...
Reexamination Certificate
2003-03-04
2004-11-02
Zalukeva, Tatyana (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Mixing of two or more solid polymers; mixing of solid...
C525S262000, C525S285000, C034S337000, C034S339000, C034S344000, C034S345000
Reexamination Certificate
active
06812296
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates to a method for the removal of free water from a sealant composition by incorporating the water into a component that is reactive with the sealant composition. Specifically, the method includes the addition of an anhydride to the sealant to react with water present in the composition and produce a total reactive system.
BREIEF DESCRIPTION OF RELATED TECHNOLOGY
Sealant compositions, especially anaerobically curable sealant compositions are known to be used in the impregnation of porous components and as threadlockers. See e.g. U.S. Pat. No. 6,231,714 to Woods et al., U.S. Pat. No. 6,093,780 to Attarwala, and U.S. Pat. No. 4,916,184 to Clark. One method of impregnating the components with the sealant composition includes immersing the component in a tank filled with the sealant composition. A vacuum or pressure means may then be added to the system to force the sealant composition into the pores of the component.
Given the nature of the method of impregnation, the tanks have a tendency to become contaminated with water as a result of exposure to the atmosphere. The water frequently forms an emulsion with the sealant composition. When this happens, the tanks of the sealant solution, which are generally clear, become cloudy. When water is present in the sealant composition, it may be introduced into the porosity of the component which interferes with the effectiveness of the sealant and decreases the speed of cure. Therefore, the contamination by water makes the sealant composition unusable requiring the disposal and replacement of the contaminated sealant or removal of the water.
Conventional methods of removing the water from the sealant composition include aerating the tanks and aerating the tanks under a vacuum. These procedures are both time-consuming and costly. Moreover, when the tanks are being aerated, they may not be used which decreases production.
A method for removing the water contaminant that is relatively less expensive than conventional methods and reduces loss in production time is needed. Methods and compositions for incorporating water into a sealant system to form a total active curable composition are particularly desirable.
SUMMARY OF THE INVENTION
One aspect of the present invention provides a method of substantially removing water from a sealant composition. This method includes the step of adding to the sealant composition an effective amount of an anhydride, which is capable of reacting with water to form a component that will not substantially interfere with the effectiveness of the sealant composition.
Another aspect of the present invention provides a method of incorporating water into a curable composition. This method includes the step of adding a component capable of reacting with water to the curable composition.
The present invention also provides a curable composition including a (meth)acrylate monomer, a component reactive with the monomer including the in situ reaction product of an anhydride and water, and a cure system for the (meth)acrylate monomer.
A further aspect of the present invention provides a curable composition including a (meth)acrylate monomer, a reactive acid component formed in situ including the reaction product of an anhydride and water, and a cure system for the(meth)acrylate monomer.
A still further aspect of the present invention provides a curable composition including the reaction product of a (meth)acrylate monomer component, a cure system for the (meth)acrylate monomer, an anhydride, and water.
A method of removing water from a curable composition is also provided that includes the step of adding to the curable composition an effective amount of a component capable of reacting with water to form an acid that is reactive with the curable composition.
DETAILED DESCRIPTION OF THE INVENTION
The methods and compositions of the present invention may be used with a variety of curable compositions, especially those including (meth)acrylate monomers, which have become contaminated with water. In order to incorporate the water into the curable composition, which may include a (meth)acrylate monomer and a cure system, an anhydride is added to the curable composition which forms a component that is reactive with the curable composition.
As used herein, the term “(meth)acrylate” or “(meth)acrylic” refers to acrylate and/or methacrylate species. The term “mono(meth)acrylate” refers to the presence of a single (meth)acrylate group, while the term “multi(meth)acrylate” refers to more than one (meth)acrylate group.
The (meth)acrylate monomer may include a mono(meth)acrylate, a multi(meth)acrylate, or a combination thereof. Specific examples of both are described in further detail below.
The multi(meth)acrylate is a polymerizable crosslinkable component. Examples of multi(meth)acrylates include ethoxylated trimethylolpropane triacrylate, trimethylol propane trimethacrylate, dipentaerythritol monohydroxypentacrylate, pentaerythritol triacrylate, ethoxylated trimethylolpropane triacrylate, 1,6-hexanedioldiacrylate, neopentyl glycol diacrylate, pentaerythritol tetraacrylate, 1,2-butylene glycol diacrylate, trimethylolpropane ethoxylate trimethacrylate, glycerol propoxylate trimethacrylate, trimethylolpropane trimethacrylate, dipentaerythritol monohydroxy pentamethacrylate, tri(propylene glycol) dimethacrylate, neopentylglycol propoxylate dimethacrylate, 1,4-butanediol dimethacrylate, polyethylene glycol dimethacrylate, triethylene glycol dimethacrylate, butylene glycol di(meth)acrylate, ethoxylated bisphenol A dimethacrylate and combinations thereof.
Examples of mono(meth)acrylates useful in the present invention include those which conform to the structure:
H
2
C=CGCO
2
R
wherein G may be hydrogen, halogen or alkyl of 1 to about 4 carbon atoms, and R may be selected from alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkaryl, aralkyl or aryl groups of 1 to about 16 carbon atoms, any of which may be optionally substituted or interrupted as the case may be with silane, silicon, oxygen, halogen, carbonyl, hydroxyl, ester, carboxylic acid, urea, urethane, carbamate, amine, amide, sulfur, sulfonate, sulfone and the like.
Examples of polar group functionalized mono(meth)acrylates include cyclohexylmethacrylate, hydroxyethyl acrylate, hydroxypropyl methacrylate, t-butylaminoethyl methacrylate, cyanoethylacrylate, and chloroethylmethacrylate. Other common monofunctional esters include alkyl esters such as lauryl methacrylate. Many lower molecular weight alkyl esters exhibit volatility, and frequently it may be more desirable to use a higher molecular weight homologue, such as decyl methacrylate or dodecyl methacrylate, or any other fatty acid acrylate esters, in (meth)acrylate-based impregnant compositions.
Hydroxyalkyl (meth)acrylates are also useful. The alkyl portion may be selected from numerous linear, branched or cyclic groups, e.g., having 1-20 carbon groups, which may also include various substitutions.
Desirably at least a portion of the (meth)acrylic monomer comprises a di- or other multi(meth)acrylate ester. These multifunctional monomers produce cross-linked polymers, which serve as more effective and more durable sealants. Various (meth)acrylate monomers may be used, such as those multi(meth)acrylate esters which have the following general formula:
wherein R
4
represents a radical selected from the group consisting of hydrogen, lower alkyl of from 1 to about 4 carbon atoms, hydroxyalkyl of from 1 to about 4 carbon atoms, and
R
3
is a radical selected from the group consisting of hydrogen, halogen, and lower alkyl of from 1 to about 4 carbon atoms; R
5
is a radical selected from hydrogen, hydroxyl, and
m may be 0 to 12, preferably from 0 to about 6; n is at least 1 (e.g., 1 to about 20 or more, preferably between about 2 to about 6); and p is 0 or 1.
Examples of these polymerizable multi(meth)acrylate esters include, but are not limited to, di-, tri- and tetraethyleneglycol dimethacrylate, dipropyleneglycol; dimethacrylate; polyethyleneglycol dimethylacrylate; di(pentameth
Chupas Peter J.
Newberth, III Frederick F.
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