CA1078992A - Paint compositions - Google Patents

Paint compositions

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Publication number
CA1078992A
CA1078992A CA284,299A CA284299A CA1078992A CA 1078992 A CA1078992 A CA 1078992A CA 284299 A CA284299 A CA 284299A CA 1078992 A CA1078992 A CA 1078992A
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CA
Canada
Prior art keywords
phenylmercury
paint
acylate
lbs
biocide
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
Application number
CA284,299A
Other languages
French (fr)
Inventor
Francis W. Arbir
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Abbott Laboratories
Original Assignee
Abbott Laboratories
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Filing date
Publication date
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Publication of CA1078992A publication Critical patent/CA1078992A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/14Paints containing biocides, e.g. fungicides, insecticides or pesticides

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

ABSTRACT OF THE DISCLOSURE:
Paint compositions containing an industrial biocide can be prevented from yellowing by the addition of a small amount of a certain mercury salt.

Description

:10'7899Z
DETAIL13D DESCRIPTIOI\~ OF Tl~lE INVl~NTION~
Certain biocides have proven useful in various paint formulations, such as exterior latex house paints. However, in certain paint formulations, particularly alkyd-modified acrylics, straight acrylics and vinyl acrylic copolymers, some commercially available paint biocides react with certain com-ponents in the paint formulation causing a transien~ yellow-ing on surfaces painted with white paint. The transient yel- ;
lowing lasts up to 72 hours and is totally unacceptable in the paint industry. The present invention provides a method for overcoming the undesirable problem by incorporating a phenyl-mercury salt into the paint formulation containing specified biocides.
In recent years, a new series of biocides have been developed and found use in many industrial applications. They are the diiodomethylsulfones, carrying alkyl, aryl, aralkyl, haloalkyl, nitroalkyl, nitrophenyl, halophenyl and halonitro-phenyl substituents on the sulfone moiety. While these bio-cides are highly effective in many indus~rial environments, they were acceptable in the paint industry only to the ex-tent of dark paints, because they develop a transient yello~-ing on white and other light-colored paints. Although this color disappears after 2 or 3 days, the yellowing effect is totally unacceptable for exterior paints. Since biocides are primarily used in exterior paints, the temporary discoloring effect caused by them essentially removed the above biocides
- 2 -~Yk `

107t3~9Z

. . .

from use in paints.
I~ has now been found that a paint composition con-taining a diiodomethyl sulfone (DIS) biocide of the formula R~SO2CHI2 wherein R is phenyl, alkylphenyl, dialkylphenyl, benzyl, chlorobenzyl, dichlorobenzyl, or an alkyl group of 2-8 carbon atoms, hereinafter referred to as R-DIS is sub-stantially completely prevented from yellowing by the addition of an acyloxy phenylmercury salt in an amount from 25 to 500%
of the amount of said biocide. The term "acyloxy phenylmer-cury salt" is intended to include those PM salts which are derived from organic mono- or dicarboxylic acids which may include a double bond in those instances where a carbon chain of more than 10 carbon atoms is involved. Typical representatives are phenylmercury acetate, phenylmercury oleate, di-(phenyl-mercury) dodecenyl succinate and other salts of this general nature. These salts can be expressed by the formula R'-COOHgC6H5 or R"-(COOHgC6H5)2 wherein R' is an alkyl chain of 1-19 and R"
is an alkylene chain of 2-18 carbon atoms, preferably contain-ing no more than one double-bond. These PM salts are effective in preventing yellowing whether the above DIS is used alone or together with a diluent as it is customary to dilute biocides of this type with 25-100% of a biologically inert material.
Often, such a diluent consists of butylated hydroxytoluenes, hereinafter referred to as BHT.
In a general embodiment of the present invention, a paint composition is made up accor~ing to known and well ac-cepted formulations except that, as the biocide, between 1 and 5 pounds of the above biocide per 100 gallon of paint
- 3 -~ormulation and an amount equal to 25-500% of said biocide amount of the above acyloxy phenylmercury salt are added. Such a paint formulation is stable to normal storage for extended periods of time and upon use thereof for coating outside sur-faces, substantially no yellowing effect can be detected.
In order to illustrate the improvement attained by the present invention, reference is made to the following examples which, however, are not intended to limit the in-vention in any respect.

White paint formulations were made up with the fol-lowing ingredients:

Water 175 lbs.
Anionic surfactant 10 5 "
Non-ionic surfactant 2 5 "
Dispersing Agent 1.5 "
Defoamers 3.0 "
Ethylene glycol 25.0 "
Hydroxyethylcellulose 2.1 "
Titanium dioxide 237.5 "
Magnesium silicate 191.4 "
These ingredients, together with the biocides listed below, were dispersed for 20 minutes at hiyh speed and then combined with a mixture of Acrylic emulsion 490.8 lbs.
Tributyl phosphate 5.0 "
Defoamer 1.0 "
Ammonia 2.0 "

,~ .
- . ..

11)78992 Ten separat~ formulations were made up containing the biocide combinations a) to e) shown helow. Fi~e of these were taken from the above paint mixture (A); the other five contained the same mixture except for using a different acrylic emulsion (B). All listed ingredients were selected from those used in standard commercial paint formulations.

a) 4 lbs. R DIS/BHT 4:1 b) 4 lbs. R-DIS/BHT 4:1 + 1.0 lb CH3COOH C6H
c) 4 lbs. R-DIS/BHT 4:1 ~ 2.0 lbs " g - d) 4 lbs. R-DIS/BHT 4:1 ~ 3.0 lbs "
e) No additive R= p-tolyl Three-mil drawdowns of the ten coatings were prepared, using a 3-mil bird blade on sealed charts. The charts were then placed under UV sunlamps and the yellowing index of the films was determined instrumentally, using a Hunter Color Dif-ference meter after exposures of 24, 48, 72, 96 and 168 hrs.
The yellowing index numbers are show~ in Table I (higher number indicates increased yellowness).
T BLE l Paint-Biocide 24 hrs. 48 hrs. 72 hrs. 96 hrs. 168 hrs~

A ~ a 13.0 16.1 19.0 19.820.3 A - b 2.1 7.0 10.4 13.918.7 A - c 1.0 1.3 1.7 5.013~2 A - d 1.0 1.3 1.3 2.1 3.2 A - e 0.7 1.0 1.0 1.0 1.2 B - a 6.3 7.5 8.3 9.610.3 B - b 1.1 1.7 1.9 2.0 2.6 B - c 1.0 1.5 1.5 1.5 1.4 B - d 0.9 1.3 1.3 1.4 1.4 B - e 1.0 1.4 1.6 1.6 1.2 1C~7899Z

.
The above ten formula~:ions were also applied to panels of white pine by brushing them on in two coats at a spreading rate of 400 ft2/gal. These panels were then exposed to direct sunlight for 10 days and the yellowness index was re-corded by 1:he apparatus of Example 1 at periodic intervals as shown in Table II.
TABLE II
;:
Paint-Biocide 8 hrs. 16 hrs. 24 hrs. 54 hrs. 102 hrs. 200 hrs. 240 hrs.

A- a10.3 11.1 11.4 4.03.9 5.7 5.9 A - b2.2 5.3 6.0 2.94.0 5.3 4.4 A- c 1.8 2.5 2.8 2.03.9 4.1 3.6 A - d2.1 3.2 2.5 1.84.0 4.2 4.3 A - e1.6 2.6 2.2 1.53.5 3.7 3.6 B - a3.1 5.5 6.4 3.34.5 5.7 5.1 B - b1.7 3.0 3.2 2.54.6 4.8 4.0 B - c2.2 2.9 3.1 1.94.5 4.5 3.9 B - d2.0 2.9 2.9 1.84.7 4.4 3.9 B - e2 1 3.4 3.2 1.84.6 4.6 4.1 Another paint formulation was prepared from the follow~

ing ingredients:

Water 250 lbs.
Anionic surfactant 8.0 "
Non-ionic surfactant2.5 "
Dispersing agent 1.0 "
Hydroxyethylcellulose2.5 "
Ethylene glycol 25.0 "
. 2-Ethoxyethanol acetate 15.0 "
Defoamers 3.0 "
Titanium dioxide 250.0 Magnesium silicate200.0 "
Biocides as shown below 107899;~
After mixing these components at high speed for 20 minutes, 400 lbs. of vinyl acrylic emulsion containing 1.0 lb. of a defoamer were blended with the above. The vinyl-acrylic paint so obtained was tested as shown in Example 2.
The yellowing index results are given in Table III, using the same biocide mixtures a) to e) shown in Example I.
TABLE III
Biocide 8 hrs. 24 hrs. 48 hrs. 96 hrs. 2~0 hrs.
_ ._ _ . . _ . .. . ... _ _ .
a 1.85.2 5.3 6.8 7.7 b 1.22.5 3.8 4.7 3.7 c 1.63.0 4.6 4.8 4.2 d 1.52.8 3.9 3.9 3.8 e 1.32.9 4.1 4.0 3.8 ... ..
By replacing the above 80% R-DIS/BHT mixture with a 50% mixture or pure 4-tolyl diiodomethyl sulfone in the above formulations, results substantially identical to those in Table III are obtained.

A paint base was made up by a 20 minute high-speed dispersion of Water 215.9 lbs.
Anionic surfactant 10.5 Non-ionic surfactant 2.5 "
Dispersing agent 1.5 "
Defoamers 3.0 "
Ethylene glycol 25.0 "
~Iydroxyethylcellulose2.3 "
Titanium dioxide 237.5 "
Magnesium silicate 237.5 "
Biocide mixture as listed , .

:: :

1078g9Z
This dispersion was blended with a mixture of Acrylic emulsion 390.8 lbs.
Long oil alkyd 30.8 Cobalt drier 0.2 "
Zirconium drier 0.6 "
Defoamer 1,0 "
Tributylphosphate 9.3 "
Ammonia 1.Q "
The results obtained with this latex house paint con-taining phenylmercury acetate (PMA) or di-(phenylmercurydodecenyl-succinate)(PMDS) according to the tests in Example 1 (A) and Example 2 (B) are shown in Table IV. In all instances, the DIS
of Example 1 was used as a mixture with butylated hydroxy-toluene containing 80% by weight of DIS. Those skilled in the - interpretation of color index differentiating measuring devices such as the above will recognize that the yellowing rates of 1 and 3 would not be distinguishable by the human eye. Thus, a reading of about 3 is still acceptable in a white paint.
Table IV also contains a mold rating (MR) column which shown, on a scale from 0 (no mold) to 4 the performance of the paint in a mold box test. In this test, the above paints were applied to tongue depressors by dipping the latter in the paint, J drying the, inoculating them with a mixture of A. pullulans, P.funiculosum and A.niger and placing them in mold boxes for four weeks at 32C and a relative humidity of 90-100%. The MR-read-ings given below are those obtained after 4 weeks.

TABLE IV
, Additives in lbs. Test A Test B
Ex.# per 100 gal.paint ~4 96 8 54 240 hrsMR
__
4 9 PMA 2.4 3.0 0.7 1.6 3.1 2
5 ~I 2.4 ~.8 1.2 1.8 3.8 3
6 1 " 2.3 2.7 1.2 1.5 3.7 4
7 7 " + 1 DIS 1.5 2.0 1.0 1.5 3.7
8 5 " + 1 " - 1.9 3.0 1.0 1.4 3.9 1
9 3 " + 1 " 1.3 1.9 1.2 1.5 3.4 0 1010 1 " + 1 " 1.3 2.1 1.4 1.6 3.9 11 7 " + 2 " 1.3 2.3 1.4 1.8 5.0 0 12 5 " +2 " 1.2 2.2 1.1 1.7 4.4 0 13 3 " + 2 " 1.1 2.5 1.9 1.8 4.4 0 14 1 " + 2 " 1.2 3.0 1.5 1.8 4.4 0 . . ..... _ _ 9PMDS 1.4 2.1 1.6 2.2 3.4 16 5 " 1.5 2.1 1.7 2.0 3.4 3 17 1 " 1.4 1.9 1.7 1.8 3.9 4 18 7 " + 1 DIS 1.4 2.0 1.7 1.7 3.6 0 19 5 " + 1 " 1.2 2.0 2.1 2.0 4.1 0 2020 3 " + 1 " 1.1 2.1 1.6 1.7 3.6 0 21 1 " + 1 " 1.6 3.0 1.8 1.9 3.8 0 22 7 " + 2 " 1.4 2.6 1.9 1.7 3.9 23 5 " + 2 " 1.5 4.3 1.4 1.7 3 5 0 24 3 " + 2 " 1.0 4.9 1.7 1.9 4 1 0 1 " + 2 " 1.4 4.9 1.8 2.2 4.3 0 . . .. _._ .
26 2 DIS 7.8 9.6 5.7 2.5 4.6 0 27 none 1.7 2.2 2.4 2.5 3.4 4 . .
The above examples clearly show that a house paint containing no biocide deteriorates rapidly when exposed to com-30 mon molds and that it therefore requires biocidal protection.
As shown, a DIS alone provides excellent protection, but it is unacceptable from the discoloration standpoint. However, a combination of a DIS with a phenylmercury salt of an organic mono-or dicarboxylic acid protects the palnt against fungal growth and against discoloration by sun light or UV light.

- g _ . , .

10789~2 The above examples all demonstrate the use of a specific DIS, namely the 4-tolyl diiodomethyl sulfone. In the following table, yellowing results are shown with paint formu- -lation drawdowns containing a DIS other than the above. In all instances, the paint formulation and preparation of Example 1 is used. Substituent R shown in Table V refers to R of the above R-DIS, and the measured yellowing index (YI).
In each example, the paint contains 4 lbs. of a DIS with (b) or without (a) and 3 lbs. of phenyl mercury acetate per 100 gallons of paint.
TABLE V
R YI after 24 hrs. YI after 48 hrs.
28 et~h~yl b 160 9 21 9 29 hexyl a 17.6 23.4 ~ b 0.8 2.0 .. . _ _ _ . .. _ . . .. _ . _ _ _ . _ _ .

Cl---- b __ 0 8 _ 1 6 31Cl ~ CH2- a 10:8 0 9 32 ~ CH2- a 10:8 0 9 .._ . ................ . _ . . . _ . . _ . _
- 10 -.

~078992 While the above examples use the R-DIS as an 80%
mixture with BHT, the same results are obtained when sub-stantially pure R-DIS is used:
The paint formulation of Example 1, emulsion B, is prepared as stated, but containing 4 pounds of tolyl-DIS and 3 pounds of phenylmercury acetate per lOQ gallons of paint.
This paint, with and without said mercury salt, was tested exactly as shown in Example 1, resulting in a yellowing index reading of 1.6 for the sample containing biocide and mercury salt and 4.8 for the sample containing the biocide alone, after 48 hours under UV light.
While the above examples demonstrate the effects with only two particular phenylmercury salts, other acyloxy phenyl-mercury salts or diacyloxy diphenylmercury salts produce sub-stantially similar results. These salts have been used before by the paint industry and are well known and easily synthesized.
However, their use to prevent the temporary yellowing caused by the use of a DIS as the biocide was a surprising and un-expected discovery.
Paint compositions containing a DIS and the above mer-curial salt are substantially completely protected against bio-logical or light degradation. The preferred range for a DIS is between 2 and 4 lbs. per 100 gallons of paint with 2 to 5 lbs.
per 100 gallons of said phenylmercury salt. While ordinarily, 5 lbs. of a DIS is the practical upper limit in 100 gallons of paint, larger amounts can sometimes be usefully employed, although : ~ .
amounts of >10 lbs/100 gallons serve no additional purpose.

Mercury salt amounts of 25~ of the amount of the bio-cide is about the lowest level that wilI prevent yellowing ~` - 11 - ' -~ "~

10~89~Z
caused by the biocide. Amounts up to 5 times the amount of the biocide can be used but on a weight basis, it would be unnecessary to exceed 10 lbs/100 gallons of paint. In some paint systems, particularly those used for interior paints in dry climates, 1 lb/100 gal. of the biocide produces sufficient protection against biological deterioration of the paint or its substrate and 0.25 lb/100 gal. of the acyloxy phenylmercury compound would be sufficient to overcome the temporary yellow-ing effect that might occur with this low level of a DIS. On the other hand, in paints designed for exterior use in humid climates, 5 lbs. of a DIS and 10 lbs. of the phenylmercury salt produce substantially full protection against biological and light deterioration or degradation. Larger amounts of either additive could be used but provide no significant benefit over the named amounts.
Aside from the mercury salts exemplified above, phenyl-mercury oleate provides the same excellent results as demon-strated in the examples. However, other acyloxy phenylmercury salts can be used in the same fashion, i.e. the phenylmercury propionate, hexanoate, decanoate, palmitate, stearate, or the di(phenylmercury)maleate, Malonate, succinate which may carry alkyl substituents in the alkylene chain between the carboxy groups.

~h:~ ~

Claims (18)

The embodiments of the invention in which an exclusive property or privilege is claimed, are defined as follows:
1. A paint composition being substantially completely prevented from biological or light degradation containing, per 100 gallons of paint, between 1 and 5 lbs. of a biocide of the formula R-SO2CHI2 wherein R is phenyl, alkylphenyl, di-alkylphenyl, benzyl, chlorobenzyl, dichlorobenzyl or an alkyl group of 2-8 carbons and between 0.25 and 5.0 lbs. per pound of said biocide a phenylmercury acylate of the formula R'-COOHgC6H5 or R"-(COOHgC6H5)2 wherein R' is an alkyl group of 1-19 carbon atoms and R" is an alkylene group of 2-18 carbon atoms, said alkyl or alkylene containing between 0 and 1 double bond.
2. A paint composition according to Claim 1 wherein said phenylmercury acylate is phenylmercury acetate.
3. A paint composition according to Claim 1 wherein said phenylmercury acylate is di-(phenylmercury) dodecenyl succinate.
4. A paint composition according to Claim 1 wherein said paint contains 2 to 4 lbs. of said biocide and between 2 and 5 lbs. of said phenylmercury acylate per 100 gallons of paint.
5. The composition of Claim 4 wherein said phenylmercury acylate is phenylmercury acetate.
6. The composition of Claim 4 wherein said phenyl-mercury acylate is di-(phenylmercury)dodecenyl succinate.
7. A paint composition being substantially completely prevented from biological or light degradation containing, per 100 gallons of paint, between 1 and 5 lbs. of the biocide 4-tolyl diiodomethyl sulfone and between 0.25 and 5.0 lbs. per pound of said biocide a phenylmercury acylate of the formula R'-COOHgC6H5 or R"-(COOHgC6H5)2 wherein R' is an alkyl group of 1-19 carbon atoms and R" is an alkylene group of 2-18 carbon atoms, said alkyl or alkylene containing between 0 and 1 double bond.
8. A paint composition according to Claim 7 wherein said phenylmercury acylate is phenylmercury acetate.
9. A paint composition according to Claim 7 wherein said phenylmercury acylate is di-(phenylmercury) dodecenyl succinate.
10. A paint composition according to Claim 7 wherein said paint contains 2 to 4 lbs. of said biocide and between 2 and 5 lbs. of said phenylmercury acylate per 100 gallons of paint.
11. The composition of Claim 7 wherein said phenyl-mercury acylate is phenylmercury acetate.
12. The composition of Claim 7 wherein said phenyl-mercury acylate is di-(phenylmercury)dodecenyl succinate.
13. The process of preventing or reducing yellowing in paint compositions containing a biocide of the formula R-SO2-CHI2 wherein R is phenyl, alkylphenyl, benzyl, chloro-benzyl, dichlorobenzyl or an alkyl group of 2-8 carbons con-sisting essentially in adding to said paint composition between 0.25 and 5.0 lbs. per pound of said biocide of a phenylmercury acylate consisting essentially of a compound having the formula R'-COOHgC6H5 or R"-(COOHgC6H5)2, wherein R is an alkyl group of 1-19 carbon atoms and R" is an alkylene group of 2-18 carbon atoms, said alkyl or alkylene containing between 0 and 1 double bond.
14. The process of claim 13 wherein said phenyl-mercury acylate is phenylmercury acetate.
15. The process of claim 13 wherein said phenyl-mercury acylate is di(phenylmercury)dodecenyl succinate.
16. The process of claim 13 wherein said phenyl-mercury acylate is added in an-amount of from 0.25 to 10 lbs.
per 100 gallons of paint.
17. The process of claim 14 wherein said phenyl-mercury acylate is phenylmercury acetate.
18. The process of claim 14 wherein said phenyl-mercury acylate is di(phenylmercury)dodecenyl succinate.
CA284,299A 1976-09-30 1977-08-08 Paint compositions Expired CA1078992A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US72833876A 1976-09-30 1976-09-30
US76339077A 1977-01-28 1977-01-28

Publications (1)

Publication Number Publication Date
CA1078992A true CA1078992A (en) 1980-06-03

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ID=27111673

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (7)

Country Link
AU (1) AU2699077A (en)
BR (1) BR7705429A (en)
CA (1) CA1078992A (en)
DE (1) DE2743860A1 (en)
DK (1) DK424077A (en)
FR (1) FR2366346A1 (en)
NL (1) NL7710126A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0034877A3 (en) * 1980-01-28 1981-09-09 General Electric Company Mildew resistant rtv silicone compositions

Also Published As

Publication number Publication date
NL7710126A (en) 1978-04-03
FR2366346A1 (en) 1978-04-28
DK424077A (en) 1978-03-31
AU2699077A (en) 1979-01-18
DE2743860A1 (en) 1978-04-06
BR7705429A (en) 1978-03-28
FR2366346B3 (en) 1980-07-18

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