CA1077190A - Stabilized adhesive and curing compositions - Google Patents
Stabilized adhesive and curing compositionsInfo
- Publication number
- CA1077190A CA1077190A CA256,609A CA256609A CA1077190A CA 1077190 A CA1077190 A CA 1077190A CA 256609 A CA256609 A CA 256609A CA 1077190 A CA1077190 A CA 1077190A
- Authority
- CA
- Canada
- Prior art keywords
- composition
- monomer
- group
- allyl
- hydroquinone
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polymerisation Methods In General (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerization Catalysts (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
ABSTRACT
Stabilized, curable compositions formed from known free radical-polymerizable monomers (e.g., acrylates, styrene, etc.), and free radical initiators (e.g., peroxides, hydroperoxides, ultraviolet-sensitive compounds) by dissolving therein compounds containing the combination of allyl lower alkoxyl and hydroxyl groups. All the groups may be present in one molecule, or the allyl group may occur in a separate molecule. Concentration of each compound may be in the range of about 0.01 to about 5 percent by weight of the total composition.
Stabilized, curable compositions formed from known free radical-polymerizable monomers (e.g., acrylates, styrene, etc.), and free radical initiators (e.g., peroxides, hydroperoxides, ultraviolet-sensitive compounds) by dissolving therein compounds containing the combination of allyl lower alkoxyl and hydroxyl groups. All the groups may be present in one molecule, or the allyl group may occur in a separate molecule. Concentration of each compound may be in the range of about 0.01 to about 5 percent by weight of the total composition.
Description
BACKGROUND OF THE INVENTION
This invention relates to adhesive compositions and, in general, curing compositions of the type wherein cure is initiated by means of peroxy compounds such as peroxides or hydroperoxides or by means of ultraviolet irradiation, and takes place by virtue of free radical polymerization. Such compounds typically contain vinyl unsaturation~
It is desirable that compositions of the kind indicated shall be stable in storage for extended periods. ~any of these composi-tions are anaerobic, i.e., undergo cure-when deprived of access to oxygen, but can be caused to cure by other means. It is desir-able that such anaerobic compositions be preserved from curing when stored in an oxygen-poor environment, in order to undergo cure later, when required, by the use of said other means.
Certain types of compounds are well known as inhibitors of premature polymerization for such compounds. Typically, these inhibitors are quinone- or hydroquinone-type compounds and their derivatives. Free radical scavengers of various types have also been used with some success.
None of these known inhibitors has proven full~ satisfactory for all uses, however, especially in connection with acryla~e and urethane-acrylate monomers such as those specifically described herein. Inhibitor systems capable of imparting significantly improved stability to free radical curinq compositions would thus have great utility.
SUMMARY OF THE INVENTION
The present invention provides inhibitor systems which pro-vide advantageous and unexpected improvements in stability.
Accordingly, the present invention provides a stabilized, curable composition comprising: ' a) A free radical-polymerizable monomer;
b) An effective amount for initiation of a peroxy or photo-sensitive initiator; and c) an effective amount for stabilization of the composition of an inhibitor system selected from the group consisting of an allyl alkoxy hydro-quinone and the combination of an allyl com-pound with an alkoxyl hydroquinone, said inhibitor system being dissolved in the monomer.
Preferred monomers are those prepared by reacting at a temperature between about 10C. and about 175C.: (i) an organic polyisocyanate; and tii) an acrylate ester containing a hydroxy or amino group in the non-acrylate portion thereof, the ester being used in sufficient amount to react with substantially all 0 f the isocyanate groups of the polyisocyanate.
Other preferred monomers are those havinq the formula O ~ /R ~ R 1 H2C=C_C_O~(CH2)mtC~R3 ~C R
wherein R6 represents a radical selected from the group consisting of hydrogen, lower alkyl of 1-4 carbon atoms, hydroxyalkyl of 1-4 carbon atoms, and o -CH2-0-C-C;CH2 Rl is a radical selected from the group consisting of hydrogen, halogen, and lower alkyl of 1-4 carbon atoms; R5 is a radical selected from the group consisting of hydrogen, --OH and O
S -O-C-C=CH2 Rl m is an integer equal to at least l; n is an integer equal to at least l; and p is 0 or l.
There is also provided a method of stabilizinq a curable composition comprising a free radical-polymerizable monomer and an effective amount for initiation of a peroxv or photo-sensitive initiator, comprising dissolving in the monomer an effective amount for stabilization of the composition of an inhibitor system;
selected from the group consisting of an allyl alkoxyl hydro-quinone and the combination of an allyl compound with an alkoxyl hydroquinone.
Photo-initiated compositions are especially benefited since, by using increased levels of the inhibitor systems, improved stability is obtained without sacrifice of desirable cure pro-perties With curable compositions which are inherently anaerobic in nature, the present inhibitor systems can effectively suppress the anaerobic cure characteristics, thereby allowing these desir- ;
able monomer compositions to be utilized in oxygen-starved appli- .
cations, such as the adhesive layer on tightly-wound tapes or in oxygen-impermeable containers such as aerosol cans.
~077190 DETAILED DESCRIPTION
OF THE INVENTION
Stabilization of free radical-curing compositions is effected by dissolving in those compositions an inhibitor system comprising a single compound or a pair of compounds having certain specific groups in the molecule.
When a single compound is used the said groups are allyl, aromatic alkoxyl and aromatic hydroxyl, and a preferred compound ; is of the formula C~2=CH-CN~ _ ~ 03 When, on the other hand, a pair of compounds is used, one member of the pair has aromatic alkoxyl and aromatic hydroxyl in the molecule, and hydro~uinone monomethyl ester, of the formula ., ~
~ 3 is preferred; the other member of the pair has the allyl group I -CH2=CH-CH2- in the molecule, and preferred compounds are triallyl' phosphate and diallyl phthalate. It is believed that in those cases where a pair of added compounds is present,the members of the pair have a mutual synergistic effect. More generally defined, the alkoxyl group may be any lower alkoxyl of one to about four carbon atoms. It will be understood that the group may also be substituted, provided only that the substituent not interfere substantially with the effectiveness of the over-all compound.
When two compounds are used, the hydroxyl and alkoxyl groups should occur in the same molecule.
1C~77190 '' ~ hile in the preferred compounds the alkoxyl group will be in the ortho position relative to the hydroxyl group, it may optionally also occur in the meta or para position. Similarly, when all three required groups occur in the same molecule, the allyl group need not necessarily be in the para position relative to the hydroxyl group, although that position is preferred. In either case, the aromatic group may be further substituted, pro-vided only that the substituent not interfere substantially with - the effectiveness of the inhibitor system.
When a separate allyl compound is used, it may be either organic or inorganic, the latter being preferred. However, reducing-type compounds, such as allyl phosphites and sulfites, should be avoided.
Representative useful compounds include, in addition to those already mentioned, triallyl orthoformate, triallyl phosphate,
This invention relates to adhesive compositions and, in general, curing compositions of the type wherein cure is initiated by means of peroxy compounds such as peroxides or hydroperoxides or by means of ultraviolet irradiation, and takes place by virtue of free radical polymerization. Such compounds typically contain vinyl unsaturation~
It is desirable that compositions of the kind indicated shall be stable in storage for extended periods. ~any of these composi-tions are anaerobic, i.e., undergo cure-when deprived of access to oxygen, but can be caused to cure by other means. It is desir-able that such anaerobic compositions be preserved from curing when stored in an oxygen-poor environment, in order to undergo cure later, when required, by the use of said other means.
Certain types of compounds are well known as inhibitors of premature polymerization for such compounds. Typically, these inhibitors are quinone- or hydroquinone-type compounds and their derivatives. Free radical scavengers of various types have also been used with some success.
None of these known inhibitors has proven full~ satisfactory for all uses, however, especially in connection with acryla~e and urethane-acrylate monomers such as those specifically described herein. Inhibitor systems capable of imparting significantly improved stability to free radical curinq compositions would thus have great utility.
SUMMARY OF THE INVENTION
The present invention provides inhibitor systems which pro-vide advantageous and unexpected improvements in stability.
Accordingly, the present invention provides a stabilized, curable composition comprising: ' a) A free radical-polymerizable monomer;
b) An effective amount for initiation of a peroxy or photo-sensitive initiator; and c) an effective amount for stabilization of the composition of an inhibitor system selected from the group consisting of an allyl alkoxy hydro-quinone and the combination of an allyl com-pound with an alkoxyl hydroquinone, said inhibitor system being dissolved in the monomer.
Preferred monomers are those prepared by reacting at a temperature between about 10C. and about 175C.: (i) an organic polyisocyanate; and tii) an acrylate ester containing a hydroxy or amino group in the non-acrylate portion thereof, the ester being used in sufficient amount to react with substantially all 0 f the isocyanate groups of the polyisocyanate.
Other preferred monomers are those havinq the formula O ~ /R ~ R 1 H2C=C_C_O~(CH2)mtC~R3 ~C R
wherein R6 represents a radical selected from the group consisting of hydrogen, lower alkyl of 1-4 carbon atoms, hydroxyalkyl of 1-4 carbon atoms, and o -CH2-0-C-C;CH2 Rl is a radical selected from the group consisting of hydrogen, halogen, and lower alkyl of 1-4 carbon atoms; R5 is a radical selected from the group consisting of hydrogen, --OH and O
S -O-C-C=CH2 Rl m is an integer equal to at least l; n is an integer equal to at least l; and p is 0 or l.
There is also provided a method of stabilizinq a curable composition comprising a free radical-polymerizable monomer and an effective amount for initiation of a peroxv or photo-sensitive initiator, comprising dissolving in the monomer an effective amount for stabilization of the composition of an inhibitor system;
selected from the group consisting of an allyl alkoxyl hydro-quinone and the combination of an allyl compound with an alkoxyl hydroquinone.
Photo-initiated compositions are especially benefited since, by using increased levels of the inhibitor systems, improved stability is obtained without sacrifice of desirable cure pro-perties With curable compositions which are inherently anaerobic in nature, the present inhibitor systems can effectively suppress the anaerobic cure characteristics, thereby allowing these desir- ;
able monomer compositions to be utilized in oxygen-starved appli- .
cations, such as the adhesive layer on tightly-wound tapes or in oxygen-impermeable containers such as aerosol cans.
~077190 DETAILED DESCRIPTION
OF THE INVENTION
Stabilization of free radical-curing compositions is effected by dissolving in those compositions an inhibitor system comprising a single compound or a pair of compounds having certain specific groups in the molecule.
When a single compound is used the said groups are allyl, aromatic alkoxyl and aromatic hydroxyl, and a preferred compound ; is of the formula C~2=CH-CN~ _ ~ 03 When, on the other hand, a pair of compounds is used, one member of the pair has aromatic alkoxyl and aromatic hydroxyl in the molecule, and hydro~uinone monomethyl ester, of the formula ., ~
~ 3 is preferred; the other member of the pair has the allyl group I -CH2=CH-CH2- in the molecule, and preferred compounds are triallyl' phosphate and diallyl phthalate. It is believed that in those cases where a pair of added compounds is present,the members of the pair have a mutual synergistic effect. More generally defined, the alkoxyl group may be any lower alkoxyl of one to about four carbon atoms. It will be understood that the group may also be substituted, provided only that the substituent not interfere substantially with the effectiveness of the over-all compound.
When two compounds are used, the hydroxyl and alkoxyl groups should occur in the same molecule.
1C~77190 '' ~ hile in the preferred compounds the alkoxyl group will be in the ortho position relative to the hydroxyl group, it may optionally also occur in the meta or para position. Similarly, when all three required groups occur in the same molecule, the allyl group need not necessarily be in the para position relative to the hydroxyl group, although that position is preferred. In either case, the aromatic group may be further substituted, pro-vided only that the substituent not interfere substantially with - the effectiveness of the inhibitor system.
When a separate allyl compound is used, it may be either organic or inorganic, the latter being preferred. However, reducing-type compounds, such as allyl phosphites and sulfites, should be avoided.
Representative useful compounds include, in addition to those already mentioned, triallyl orthoformate, triallyl phosphate,
2-allyl phenol, 4-allyl-2,6-dimethoxy phenol, 2-allyl-6-methyl phenol, and 2-allyl-4-methyl phenol, among others.
It is necessary that the inhibitor system be soluble in the monomeric composition in the concentrations used. When the in-hibitor system comprises a single compound, its concentrationshould be in the range of about O.Ol percent to about 5 percent by weight of the total curable composition. Preferably, its concentration will be about 0.02 percent to about 2 percent, and more preferably about 0.025 to about 0.5 percent by weight of the total curable composition.
When the inhibitor system comprises two compounds, the con-centration of each of them may be in the range of about O.Ol percent to about 5 percent by weight oE the total curable com-position. Preferably, the concentration of the allyl compound will be in the range of about O.l percent to about 4 percent, .
1(~77~90 and more preferably about l to about 2 percent. Preferably, the concentration of the alkoxyl phenol will be about 0.1 to about 3 percent, and more preferably about 0.2 to ahout 0.4 percent by weight of the total curable composition. The ratio of the allyl compound to the alkoxyl phenol compound may vary over a rather wide range, typically from about 0.1:1 to about lO:l, respectively, preferably about l:l to about 5:1, respectively. For those curable compositions which are anaerobic in nature, it has been observed that the anaerobic cure characteristics become progress-ively more inhibited the closer the ratio comes to l:l.
~ ecause of the large number of curable monomeric compoundswhich may be stabilized by the present invention, it is not practical to specify concentration ranges and ratios of compounds in more than general terms. In any given case, appropriate con-centrations and/or ratios may be readily determined by simpleexperimentation.
As has been stated, the threshold requirement is that the inhibitor system be soluble in the monomeric composition. This, of course, may be easily ascertained. Effectiveness as a stabil-izer against premature polymerization may be easily determined ~by storing a small quantity of curable composition containing theinhibitor system at room temperature, or at an elevated tempera-ture if an accelerated test is desired, and observin~ the length of time elapsed before the composition begins to gel, i.e., cure or polymerize. While the selection of test temperature is basically a matter of convenience, it has been found that 82C. is a parti-cularly useful temperature for acrylate and methacrylate adhesive/
sealant compositions formulated with hydroperoxy initiators. In such systems, a no-gel period of one hour or more at 82C. indi-cates a probable shelf-life of one year or more at room temperature.
~077190 Other temperatures at which thermal stability is customarily measured include 65C., 55C and 37C.
As has been mentioned, the present inhibitor systems are effective in stabilizing a wide variety of monomeric, cur-able compositions. Thus, a useful stabilizing effect will be observed with curable compositions based upon aromatic monomers such as styrene, vinyl monomers such as butadiene, vinyl chloride and vinylidene chloride, acrylate/methacrylate-type monomers such as methylmethacrylate, ethyleneglycol diacrylate, bisphenol-A dimethacrylate, hydroxypropyl methacrylate, and the like, such as those taught in U.S.P. 2,895,950. Included among the lattertype are the urethane-acrylates/methacrylates, such as those taught by Gorman et al in U.S.P. 3,425,988, those disclosed in Canadian Patent No. 1,009,792, granted Mav 3, 1977, as well as those taught in Canadian Patent No. 1,052,032, granted April 3, 1979 and in copending Canadian applications No.
243,813, filed January 20, 1976 and No. 247,216, filed March 5, 1976.
~lonomers of the preceding types are curable by free radical polymerization using any of numerous well-known initiators as a source of free radicals. Among such initiators there may be mentioned peroxides such as hydrogen peroxide and oryanic peroxides such as benzoyl peroxide and me~hylethyl ketone peroxide; azo-compounds such as 2,2'-azobis(isobutyro-nitrile); hydroperoxides cumene hydroperoxide, t-butyl hydro-peroxide and methylethyl ketone hydroperoxide; peresters which hydrolyze to peroxy compounds, such as t-butyl perbenzoate and t-butyl peracetate; and photo-sensitive compounds such as benzophenone and the benzoin ethers.
As will be appreciated, the concentration of such initiator in any given curable system will be a matter of choice and well ~ . :
1077~90 within the skill of the art to determine. As a general rule, the initiator concentration will be in the range of about 0.1 percent to about 10 percent by weight of the total curable composition.
As to the photo-sensitive (i.e., ultraviolet-sensitive) types of initiator systems, it is a particular advantage of the present inhibitor systems that they may optionally be utilized in sub-stantially increased concentration without significantly inter-fering with the W -initiated cure properties. Thus, the inhibitor system concentration may be increased by 4-5-fold, or more, over the lowest commercially useful level, thereby obtaining an out-standingly stable composition but yet without destroying its cure speed. In selecting photo-initiators, a degree of care should be exercised to avoid creating an interactive initiator-inhibitor combination which could impair the effectiveness of either.
Thus, for example, the combination of benzoin ethers with the monoethyl ether of hydroquinone should be avoided since these have been found to interact.
The curable stabilized compositions of this invention may be modified by inclusion of any of numerous known additives such as polymerization accelerators (e.g., amides, imides and amines), diluents, viscosity regulators, plasticizers, dyes, etcO, provided only that such additives do not significantly interfere with the effectiveness of the present inhibitor systems.
E X A M P L E S
The following examples are intended to be illustrative, but not limiting, of the present invention.
Example 1:
This example shows how the thermal stability of a styrene-based composition of the prior art (1) compares with that of two ~077~90 similar compositions (2), (3) according to the invention.
Thermal stability (hours) Parts by Weight 55C. 65C.
(1) Styrene 95.0 Benzoyl peroxide 5.0 19 6 (2) Styrene 93.8 Benzoyl peroxide 5.0 Triallyl phosphate 1.0 Hydroquinone mono-methyl ether 0.2 76 19 ~3) Styrene 92.6 Benzoyl peroxide 5.0 Triallyl phosphate 2.0 Hydroquinone mono- ;
methyl ether 0.4 140 27 Compo$ition (1) would normally also contain a conventional hydro-quinone-type polymerization inhibitor which can be omitted from (2~ and (3). All three compositions were readily polymerizable by techniques standard in styrene technology.
Example 2: 1 This example shows how the thermal stability of a polyethylene-glycol dimethacrylate-based composition of the prior art (4) com-pares with that of a similar composition (5) according to the ~invention.
(4) (5) Polyethylene glycol dimethacrylate 95.2 94.0 parts by weight Saccharin 0.4 0.4 parts by weight 30 Cumene Hydroperoxide 4.0 4.0 parts by weight N,N-dimethyl-p-toluidine 0.4 0.4 parts by weight Hydroquinone monomethyl ether (M.E.H.Q.) Nil 0.2 parts by weight Triallyl phosphate Nil 1.0 parts by weight 35 Thermal stability at 82C.
(minutes) 30 72 _ g _ .
10771~0 These compositions are inherently anaerohic in nature, i.e., rapid cure is achieved only in the absence of oxygen. In order to test their anaerobic cure characteristics, a few drops of each composi-tion were applied to the threads of mating black oxide nuts and bolts, the nuts and bolts were assembled (thereby excluding oxygen)~, and cure was allowed to proceed. Both compositions developed satisfactory cured properties; however, it was found that the cure speed of composition (5), while commercially usable, was slower than that of composition (4) of the prior art. (Appropriate tests for anaerobic cure propert es are well described in the literature, e.g., U.S. Patents 2,895,950 and 3,043,820.
Example 3:
This example shows how the thermal stability of a trimethylol propane trimethacrylate-based composition of the prior art (6) com-pares with that of a similar composition (7) according to the invention.
(6) (7) Trimethylol propane trimethacrylate 95.093.8 parts by weight 20 Benzoyl peroxide 5.0 5.0 parts by weight Triallyl phosphate Nil l.0 parts by weight M.E.H.Q. Nil 0.2 parts by weight 'rhermal stability at 55C. < 8 hours ~ 24 hours 65C. C l hour ~ 4 hours ` 82C. 50 minutes > lO0 minutes It was found that compositions (2), (3), (5) and (7) couldbe packed safely in high density polythene containers almost com-pletely full, whereas the prior art compositions (l), (4) and (6) ' , '~' ' ~
7~30 , had to be packed in partly filled low density polythene containers if premature polymerization due to oxygen exclusion were to be avoided.
Example 4:
This example relates to a typical ultraviolet light initiat-able curing composition of the prior art (8) and a similar compo-sition according to the invention (9). In both, a representative ; monomer A (in the conventional sense which includes oligomers) is used having the formula , ~ -CH3 ~ _ -C(CH ) CH2=C(CH3)COOC3H6OCONH ~ -NHCOO - ~ 3 2 This monomer A may be obtained by reactina 1 mole (120g) of hydro-genated Bisphenol-A (i.e., 4,4'-Dicyclohexanolyl dimethyl methane) with two moles (174g) of toluene 2,4-diisocyanate, and reacting the product with 2 moles (144g) of 3-hydroxypropyl methacrylate.
(8) (9) Monomer A 93.091.0 parts by weight Benzophenone 5.05.0 parts by weight Acrylic Acid 2.02.0 parts by weight Triallyl phosphate Nil1.0 parts by weight 20 M.E.H.Q. Nil1.0 parts by weight Composition (8) polymerizes either on deprivation of oxygen or on irradiation by ultra-violet light o~ suitable intensity, whereas composition (9) polymerizes only on irradiation, the anaerobic polymerization tendency having been substantially suppressed.
'' ~ .:
:1~77~90 Thus the new composition (9) can be applied to tapes which are afterwards coiled into rolls for use. This would not be possible for composition (8) unless expensive extra precautions were taken.
This invention is not limited by or to the details of the specific examples given, many of which can undergo wide variation without departing from the scope of the invention.
' ~ .
, ~ ' . '
It is necessary that the inhibitor system be soluble in the monomeric composition in the concentrations used. When the in-hibitor system comprises a single compound, its concentrationshould be in the range of about O.Ol percent to about 5 percent by weight of the total curable composition. Preferably, its concentration will be about 0.02 percent to about 2 percent, and more preferably about 0.025 to about 0.5 percent by weight of the total curable composition.
When the inhibitor system comprises two compounds, the con-centration of each of them may be in the range of about O.Ol percent to about 5 percent by weight oE the total curable com-position. Preferably, the concentration of the allyl compound will be in the range of about O.l percent to about 4 percent, .
1(~77~90 and more preferably about l to about 2 percent. Preferably, the concentration of the alkoxyl phenol will be about 0.1 to about 3 percent, and more preferably about 0.2 to ahout 0.4 percent by weight of the total curable composition. The ratio of the allyl compound to the alkoxyl phenol compound may vary over a rather wide range, typically from about 0.1:1 to about lO:l, respectively, preferably about l:l to about 5:1, respectively. For those curable compositions which are anaerobic in nature, it has been observed that the anaerobic cure characteristics become progress-ively more inhibited the closer the ratio comes to l:l.
~ ecause of the large number of curable monomeric compoundswhich may be stabilized by the present invention, it is not practical to specify concentration ranges and ratios of compounds in more than general terms. In any given case, appropriate con-centrations and/or ratios may be readily determined by simpleexperimentation.
As has been stated, the threshold requirement is that the inhibitor system be soluble in the monomeric composition. This, of course, may be easily ascertained. Effectiveness as a stabil-izer against premature polymerization may be easily determined ~by storing a small quantity of curable composition containing theinhibitor system at room temperature, or at an elevated tempera-ture if an accelerated test is desired, and observin~ the length of time elapsed before the composition begins to gel, i.e., cure or polymerize. While the selection of test temperature is basically a matter of convenience, it has been found that 82C. is a parti-cularly useful temperature for acrylate and methacrylate adhesive/
sealant compositions formulated with hydroperoxy initiators. In such systems, a no-gel period of one hour or more at 82C. indi-cates a probable shelf-life of one year or more at room temperature.
~077190 Other temperatures at which thermal stability is customarily measured include 65C., 55C and 37C.
As has been mentioned, the present inhibitor systems are effective in stabilizing a wide variety of monomeric, cur-able compositions. Thus, a useful stabilizing effect will be observed with curable compositions based upon aromatic monomers such as styrene, vinyl monomers such as butadiene, vinyl chloride and vinylidene chloride, acrylate/methacrylate-type monomers such as methylmethacrylate, ethyleneglycol diacrylate, bisphenol-A dimethacrylate, hydroxypropyl methacrylate, and the like, such as those taught in U.S.P. 2,895,950. Included among the lattertype are the urethane-acrylates/methacrylates, such as those taught by Gorman et al in U.S.P. 3,425,988, those disclosed in Canadian Patent No. 1,009,792, granted Mav 3, 1977, as well as those taught in Canadian Patent No. 1,052,032, granted April 3, 1979 and in copending Canadian applications No.
243,813, filed January 20, 1976 and No. 247,216, filed March 5, 1976.
~lonomers of the preceding types are curable by free radical polymerization using any of numerous well-known initiators as a source of free radicals. Among such initiators there may be mentioned peroxides such as hydrogen peroxide and oryanic peroxides such as benzoyl peroxide and me~hylethyl ketone peroxide; azo-compounds such as 2,2'-azobis(isobutyro-nitrile); hydroperoxides cumene hydroperoxide, t-butyl hydro-peroxide and methylethyl ketone hydroperoxide; peresters which hydrolyze to peroxy compounds, such as t-butyl perbenzoate and t-butyl peracetate; and photo-sensitive compounds such as benzophenone and the benzoin ethers.
As will be appreciated, the concentration of such initiator in any given curable system will be a matter of choice and well ~ . :
1077~90 within the skill of the art to determine. As a general rule, the initiator concentration will be in the range of about 0.1 percent to about 10 percent by weight of the total curable composition.
As to the photo-sensitive (i.e., ultraviolet-sensitive) types of initiator systems, it is a particular advantage of the present inhibitor systems that they may optionally be utilized in sub-stantially increased concentration without significantly inter-fering with the W -initiated cure properties. Thus, the inhibitor system concentration may be increased by 4-5-fold, or more, over the lowest commercially useful level, thereby obtaining an out-standingly stable composition but yet without destroying its cure speed. In selecting photo-initiators, a degree of care should be exercised to avoid creating an interactive initiator-inhibitor combination which could impair the effectiveness of either.
Thus, for example, the combination of benzoin ethers with the monoethyl ether of hydroquinone should be avoided since these have been found to interact.
The curable stabilized compositions of this invention may be modified by inclusion of any of numerous known additives such as polymerization accelerators (e.g., amides, imides and amines), diluents, viscosity regulators, plasticizers, dyes, etcO, provided only that such additives do not significantly interfere with the effectiveness of the present inhibitor systems.
E X A M P L E S
The following examples are intended to be illustrative, but not limiting, of the present invention.
Example 1:
This example shows how the thermal stability of a styrene-based composition of the prior art (1) compares with that of two ~077~90 similar compositions (2), (3) according to the invention.
Thermal stability (hours) Parts by Weight 55C. 65C.
(1) Styrene 95.0 Benzoyl peroxide 5.0 19 6 (2) Styrene 93.8 Benzoyl peroxide 5.0 Triallyl phosphate 1.0 Hydroquinone mono-methyl ether 0.2 76 19 ~3) Styrene 92.6 Benzoyl peroxide 5.0 Triallyl phosphate 2.0 Hydroquinone mono- ;
methyl ether 0.4 140 27 Compo$ition (1) would normally also contain a conventional hydro-quinone-type polymerization inhibitor which can be omitted from (2~ and (3). All three compositions were readily polymerizable by techniques standard in styrene technology.
Example 2: 1 This example shows how the thermal stability of a polyethylene-glycol dimethacrylate-based composition of the prior art (4) com-pares with that of a similar composition (5) according to the ~invention.
(4) (5) Polyethylene glycol dimethacrylate 95.2 94.0 parts by weight Saccharin 0.4 0.4 parts by weight 30 Cumene Hydroperoxide 4.0 4.0 parts by weight N,N-dimethyl-p-toluidine 0.4 0.4 parts by weight Hydroquinone monomethyl ether (M.E.H.Q.) Nil 0.2 parts by weight Triallyl phosphate Nil 1.0 parts by weight 35 Thermal stability at 82C.
(minutes) 30 72 _ g _ .
10771~0 These compositions are inherently anaerohic in nature, i.e., rapid cure is achieved only in the absence of oxygen. In order to test their anaerobic cure characteristics, a few drops of each composi-tion were applied to the threads of mating black oxide nuts and bolts, the nuts and bolts were assembled (thereby excluding oxygen)~, and cure was allowed to proceed. Both compositions developed satisfactory cured properties; however, it was found that the cure speed of composition (5), while commercially usable, was slower than that of composition (4) of the prior art. (Appropriate tests for anaerobic cure propert es are well described in the literature, e.g., U.S. Patents 2,895,950 and 3,043,820.
Example 3:
This example shows how the thermal stability of a trimethylol propane trimethacrylate-based composition of the prior art (6) com-pares with that of a similar composition (7) according to the invention.
(6) (7) Trimethylol propane trimethacrylate 95.093.8 parts by weight 20 Benzoyl peroxide 5.0 5.0 parts by weight Triallyl phosphate Nil l.0 parts by weight M.E.H.Q. Nil 0.2 parts by weight 'rhermal stability at 55C. < 8 hours ~ 24 hours 65C. C l hour ~ 4 hours ` 82C. 50 minutes > lO0 minutes It was found that compositions (2), (3), (5) and (7) couldbe packed safely in high density polythene containers almost com-pletely full, whereas the prior art compositions (l), (4) and (6) ' , '~' ' ~
7~30 , had to be packed in partly filled low density polythene containers if premature polymerization due to oxygen exclusion were to be avoided.
Example 4:
This example relates to a typical ultraviolet light initiat-able curing composition of the prior art (8) and a similar compo-sition according to the invention (9). In both, a representative ; monomer A (in the conventional sense which includes oligomers) is used having the formula , ~ -CH3 ~ _ -C(CH ) CH2=C(CH3)COOC3H6OCONH ~ -NHCOO - ~ 3 2 This monomer A may be obtained by reactina 1 mole (120g) of hydro-genated Bisphenol-A (i.e., 4,4'-Dicyclohexanolyl dimethyl methane) with two moles (174g) of toluene 2,4-diisocyanate, and reacting the product with 2 moles (144g) of 3-hydroxypropyl methacrylate.
(8) (9) Monomer A 93.091.0 parts by weight Benzophenone 5.05.0 parts by weight Acrylic Acid 2.02.0 parts by weight Triallyl phosphate Nil1.0 parts by weight 20 M.E.H.Q. Nil1.0 parts by weight Composition (8) polymerizes either on deprivation of oxygen or on irradiation by ultra-violet light o~ suitable intensity, whereas composition (9) polymerizes only on irradiation, the anaerobic polymerization tendency having been substantially suppressed.
'' ~ .:
:1~77~90 Thus the new composition (9) can be applied to tapes which are afterwards coiled into rolls for use. This would not be possible for composition (8) unless expensive extra precautions were taken.
This invention is not limited by or to the details of the specific examples given, many of which can undergo wide variation without departing from the scope of the invention.
' ~ .
, ~ ' . '
Claims (18)
1. A stabilized, curable composition comprising:
a) A free radical-polymerizable monomer;
b) An effective amount for initiation of a peroxy or photo-sensitive initiator; and c) An effective amount for stabilization of the composition of an inhibitor system selected from the group consisting of an allyl alkoxyl hydroquinone and the combination of an allyl compound with an alkoxyl hydroquinone, said in-hibitor system being dissolved in the monomer.
a) A free radical-polymerizable monomer;
b) An effective amount for initiation of a peroxy or photo-sensitive initiator; and c) An effective amount for stabilization of the composition of an inhibitor system selected from the group consisting of an allyl alkoxyl hydroquinone and the combination of an allyl compound with an alkoxyl hydroquinone, said in-hibitor system being dissolved in the monomer.
2. A composition of Claim 1 wherein the monomer is a vinyl compound.
3. A composition of Claim 1 wherein the monomer is an acry-late ester.
4. A composition of Claim 3 wherein the monomer is a meth-acrylate ester.
5. A composition of Claim 1 wherein the monomer is a urethane-acrylate adduct.
6. A composition of Claim 5 wherein the monomer is an adduct of bisphenol-A or hydrogenated bisphenol-A and an aromatic poly-isocyanate capped with a hydroxyalkyl methacrylate.
7. A composition of Claim 3 wherein the monomer has the formula wherein R6 represents a radical selected from the group consisting of hydrogen, lower alkyl of 1-4 carbon atoms, hydroxyalkyl of 1-4 carbon atoms, and R4 is a radical selected from the group consisting of hydrogen, halogen, and lower alkyl of 1-4 carbon atoms; R5 is a radical selected from the group consisting of hydrogen, -OH and m is an integer equal to at least 1; n is an integer equal to at least 1; and p is 0 or 1.
8. A composition of Claim 5 wherein the monomer is a poly-merizable monomer prepared by reacting, at a temperature between about 10°C. and about 175°C.: (i) an organic polyisocyanate; and (ii) an acrylate ester containing a hydroxy or amino group in the non-acrylate portion thereof, the ester being used in suffi-cient amount to react with substantially all of the isocyanate groups of the polyisocyanate.
9. A composition of Claim 1 wherein the initiator is an organic peroxide.
10. A composition of Claim 1 wherein the initiator is an organic hydroperoxide.
11. A composition of Claim 1 wherein the initiator is a perester.
12. A composition of Claim 1 wherein the inhibitor system is a mixture of an inorganic allyl compound and a hydroquinone com-pound of the formula where R is an alkyl group having 1 to about 4 carbon atoms.
13. A composition of Claim 12 wherein R is methyl.
14. A composition of Claim 1 wherein the inhibitor system is a compound having the formula wherein R is an alkyl group having 1 to about 4 carbon atoms.
15. A composition of Claim 14 wherein R is methyl.
16. A composition of Claim 13 wherein the inhibitor system is a mixture of hydroquinone monomethyl ether and triallyl phosphate.
17. A composition of Claim 15 wherein the inhibitor system is 4-allyl-2-methoxy-phenol.
18. A mthod of stabilizing a curable composition comprising a free radical-polymerizable monomer and an effective amount for initiation of a peroxy or photo-sensitive initiator, comprising dissolving in the monomer an effective amount for stabilization of the composition of an inhibitor system selected from the group consisting of an allyl alkoxyl hydroquinone and the combination of an allyl compound with an alkoxyl hydroquinone.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IE153075A IE42438B1 (en) | 1975-07-09 | 1975-07-09 | Stabilized curable compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1077190A true CA1077190A (en) | 1980-05-06 |
Family
ID=11028583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA256,609A Expired CA1077190A (en) | 1975-07-09 | 1976-07-08 | Stabilized adhesive and curing compositions |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS5210393A (en) |
| AU (1) | AU512819B2 (en) |
| CA (1) | CA1077190A (en) |
| DE (1) | DE2631007A1 (en) |
| FR (1) | FR2362188A1 (en) |
| GB (1) | GB1547481A (en) |
| IE (1) | IE42438B1 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4964938A (en) * | 1987-04-13 | 1990-10-23 | Dymax Corporation | Bonding method using photocurable acrylate adhesive containing perester/tautomeric acid adhesion promoter |
| JPS6420283A (en) * | 1987-07-14 | 1989-01-24 | Toa Gosei Chem Ind | Adhesive composition |
| JP3040032B2 (en) * | 1992-03-27 | 2000-05-08 | 日東電工株式会社 | Pressure-sensitive adhesives having excellent heat resistance, their adhesive sheets, and their production methods |
| DE4406858A1 (en) * | 1994-03-02 | 1995-09-07 | Thera Ges Fuer Patente | Prepolymers and free-radically polymerizable preparations made therefrom and processes for their preparation |
| GB0505909D0 (en) * | 2005-03-23 | 2005-04-27 | Univ Leeds | Formulations |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3868409A (en) * | 1969-09-24 | 1975-02-25 | Broadview Chem Corp | Acrylic acid esters |
| US4009044A (en) * | 1975-03-07 | 1977-02-22 | Vasily Vladimirovich Korshak | Adhesive composition |
-
1975
- 1975-07-09 IE IE153075A patent/IE42438B1/en unknown
-
1976
- 1976-07-06 AU AU15621/76A patent/AU512819B2/en not_active Expired
- 1976-07-08 CA CA256,609A patent/CA1077190A/en not_active Expired
- 1976-07-08 FR FR7620863A patent/FR2362188A1/en active Granted
- 1976-07-09 GB GB2863076A patent/GB1547481A/en not_active Expired
- 1976-07-09 JP JP8182276A patent/JPS5210393A/en active Granted
- 1976-07-09 DE DE19762631007 patent/DE2631007A1/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| IE42438B1 (en) | 1980-08-13 |
| JPS5210393A (en) | 1977-01-26 |
| JPS6131122B2 (en) | 1986-07-18 |
| FR2362188B1 (en) | 1981-10-09 |
| DE2631007A1 (en) | 1977-01-20 |
| IE42438L (en) | 1977-01-09 |
| GB1547481A (en) | 1979-06-20 |
| AU512819B2 (en) | 1980-10-30 |
| FR2362188A1 (en) | 1978-03-17 |
| AU1562176A (en) | 1978-01-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4100141A (en) | Stabilized adhesive and curing compositions | |
| CA1062846A (en) | Hydrazine derivative accelerator for acrylate ester adhesive and sealant composition | |
| US4380613A (en) | Gasketing and sealing composition | |
| US3988299A (en) | Anaerobic adhesive composition having improved strength at elevated temperature consisting of unsaturated diacrylate monomer and maleimide additive | |
| US4321349A (en) | Accelerator for curable compositions | |
| IE43811B1 (en) | Curable acrylate ester compositions containing hydrazine acelerators and acid co-accelerators | |
| US5618857A (en) | Impregnation sealant composition of superior high temperature resistance, and method of making same | |
| US3682875A (en) | Stabilized anaerobic sealant composition | |
| US4964938A (en) | Bonding method using photocurable acrylate adhesive containing perester/tautomeric acid adhesion promoter | |
| CA2029848A1 (en) | Stable thiolene compositions | |
| CA1077190A (en) | Stabilized adhesive and curing compositions | |
| US7067601B2 (en) | Multi-functional alpha-alkoxyalkyl acrylate and methacrylate ester compositions and reworkable polymers formed therefrom | |
| US4540738A (en) | Acrylic adhesive composition comprising an alpha amino phosphonic acid or salt having improved stability | |
| US7146897B1 (en) | UV/visible light and anaerobic curable composition | |
| CA1096535A (en) | Initiator for anaerobic compositions | |
| US4442267A (en) | Heat resistant toughened adhesive composition | |
| US4103081A (en) | Stabilized anaerobic adhesives | |
| US5281641A (en) | Dental or surgical adhesive filler | |
| US3651036A (en) | Stable anaerobic curable sealing compositions containing zinc chloride and tetrahydroquinoline | |
| US5039715A (en) | Photocurable acrylate adhesive containing perester/tautomeric acid adhesion promoter | |
| JPS5913555B2 (en) | Heat-resistant curable formulation | |
| CA1207944A (en) | Fast curing phosphate modified anaerobic composition | |
| KR20200067151A (en) | Curing accelerator for anaerobic curable composition | |
| US4812497A (en) | Anaerobically curable composition having a good stability | |
| CA1212199A (en) | Hot strength cyanoacrylate adhesive composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |