Patent Grant
10442758
The invention relates to new chemical compounds—zinc and copper salts with organic acids, which can find application as biocides.
Various zinc and copper compounds exhibiting biocidal activity are known in the art, in particular, zinc and copper oxides and inorganic salts (RU 95102413, C09D 5/14, 1997; RU 2162870, C09D 5/02, C09D 5/14, 2001; RU 2395548, C09D 5/14, B82B 1/00, 2010; RU 2398804, C09D 5/14, A01N 59/00, A01N 47/00, B82B 1/00, 2010; U.S. Pat. No. 5,540,954, A01N 59/16, A01N 59/20, B27K 3/52, B05D 07/06, A01N 31/08, A01N 31/00, 1996; U.S. Pat. No. 6,858,658, A01N 59/20, A01N 59/16, C09D 5/16, C08K 03/10, C08K 03/18, C08K 03/22, 2005; US 20080219944, C09D 5/16, 2008; US 20090223408, C09D 5/16, C09D 5/14, 2009), zinc and copper naphthenates or resinates (RU 2377121, B27K 3/50, B27K 3/52, B27K 3/22, 2009; EP 2161316, C09D 133/06, C09D 133/12, C09D 143/04, C09D 5/16, C09D 7/12, 2010; EP 2360214, C09D 143/04, C09D 193/04, C09D 5/16, 2011; U.S. Pat. No. 4,258,090, C04B 41/45, C04B 41/52, C04B 41/60, C04B 41/70, B05D 03/02, 1981), ammonia complexes of zinc salts (U.S. Pat. No. 5,460,644, C08K 3/10, C08K 3/00, C09D 5/14, C09D 5/00, 1995), zinc and copper pyrithionates (bis-(2-pyridylthio)-1,1′-dioxides) (RU 2111993, C09D 5/14, C09D 5/16, 1998; RU 2415168, C09D5/16, C09D5/14, 2011; U.S. Pat. No. 5,185,033, C09D 5/14, C09D 5/16, 1993; U.S. Pat. No. 5,298,061, C09D 5/16, C09D 5/14, 1994; U.S. Pat. No. 5,717,007, C09D 5/16, C08L, 33/10, C08K 05/17, C08K 05/18, 1998; U.S. Pat. No. 6,399,560, A01N 43/40, A01N 43/34, A61L 2/18, C11D 3/48, 2002; U.S. Pat. No. 7,410,553, D21C 5/02, B32B 27/04, D21G 1/02, 2008). The above mentioned compounds were used with various degrees of efficiency as additives to coatings intended for treatment of building structures, prevention of underwater structures and ship parts from fouling as well as for paper and wood treatment.
The closest analogue of the proposed compounds is zinc salt with acetic and methacrylic acids, i.e. zinc methacrylate-acetate (hereinafter referred to as ZMA) exhibiting a certain biocidal activity when compounded with aqueous styrene-acrylic dispersion being used as polymer primer for applying paint coatings to various surfaces (RU 2315793, C09D 5/14, C09D 131/02, C09D 133/10, 2008).
To provide new means effecting on various biological substrates, there is proposed zinc or copper (II) salt having the general formula:
wherein M is Zn or Cu,
R1 is selected from the group comprising hydrogen and methyl,
R2 is selected from the group comprising hydrogen and OH,
R3 is selected from the group comprising alkyl and SO2OH group.
To solve the same problem it is proposed to use as a biocide zinc or copper 11 salt having the general formula:
wherein M is Zn or Cu,
R1 is selected from the group comprising hydrogen and methyl,
R2 is selected from the group comprising hydrogen and OH,
R4 is selected from the group comprising hydrogen, alkyl and SO2OH group. It was surprisingly found that zinc and copper (II) salts corresponding to formula (2) which covers new compounds of formula (1), as well as formerly known zinc acrylate-benzoate and copper methacrylate-benzoate (CN 102167775, 2011), the biocidal activity of which has not been known before, have much higher biocidal activity than ZMA and, besides, wide spectrum of effect on biological matters. Thus, they can be used not only in coating compositions but also in disinfectant compositions of various purpose, paper and wood treatment compositions, polymer compositions with higher fungus resistance as well as in many methods preventing organisms and materials from adverse effect of biological matters.
The essence of the invention is illustrated by examples given below. Examples 1-8 describe the preparation and properties of certain representatives of the proposed series of substances, examples 9-23—their bactericidal and fungicidal activity.
10 g of sulfosalicylic acid, 100 ml of distilled water are placed into a 500 ml round-bottom flask and the solution is stirred until sulfosalicylic acid is completely dissolved. Then a suspension of 3.64 g of zinc oxide in 50 ml of distilled water is gradually added to the solution under constant stirring and whereupon 3.2 g of acrylic acid is added and stirred until the suspension is completely dissolved. The obtained solution is evaporated to dryness at a temperature of not more than 70° C., and the resulted solid product is subjected to recrystallization from distilled water, 12.1 g of water-soluble powdered zinc acrylate-sulfosalicylate is obtained which corresponds to the above general formula wherein R1═H, R2═SO2OH, R3═OH (79% yield of the stoichiometric). The results of elemental analysis of salts obtained as described in this and subsequent examples are given in Table 1.
Zinc methacrylate-benzoate (R1═CH3, R2═H, R3═H) with melting point of 283° C. is obtained in 68% yield of the stoichiometric by analogy with Example 1 using benzoic and methacrylic acids instead of sulfosalicylic and acrylic ones (respectively).
Zinc methacrylate-salicylate (R1═CH3, R2═OH) with melting point of 250° C. is obtained in 80% yield of the stoichiometric by analogy with Example 1 using salicylic and methacrylic acids instead of sulfosalicylic and acrylic ones (respectively).
Zinc methacrylate-sulfosalicylate (R1═CH3, R2═SO2OH, R3═OH) with melting point of 238° C. is obtained in 82% yield of the stoichiometric by analogy with Example 1 using methacrylic acid instead of acrylic one.
Zinc methacrylate-toluylate (R1═CH3, R2═CH3, R3═H) is obtained in 80% yield of the stoichiometric by analogy with Example 1 using toluylic and methacrylic acids instead of sulfosalicylic and acrylic ones respectively).
Zinc acrylate-benzoate (R1═H, R2═H, R3═H) with melting point of 238° C. is obtained in 55% yield of the stoichiometric by analogy with Example 1 using benzoic acid instead of sulfosalicylic one. The structure of the obtained individual compound is verified by NMR spectra analysis, in NMR spectrum 1H, multiplets in the regions 5.62÷5.72 and 6.15÷6.30 ppm belong to protons of H2C═CH—C(O)O acrylate group. Benzoic group displays signals at δH 7.38 (triplet), 7.48 (triplet) and 8.06 ppm (doublet). In NMR spectrum 13C, benzoic group displays signals at δC 129.0 (m-CH), 131.0 (o-CH), 132.8 (p-CH), 135.2 (C1), 175.4 ppm (OC(═O)), and acrylate group displays signals at δC 129.0 and 133.2 (H2C═CH—), 175.1 ppm (OC(═O)).
Copper acrylate-benzoate (R1═H, R2═H, R3═H) is obtained in 55% yield of the stoichiometric by analogy with Example 1 using benzoic acid instead of sulfosalicylic one and copper oxide instead of zinc oxide.
Copper methacrylate-salicylate (R1═CH3, R2═H, R3═OH) is obtained in 85% yield of the stoichiometric by analogy with Example 1 using salicylic and methacrylic acids instead of sulfosalicylic and acrylic ones (respectively) and copper oxide instead of zinc oxide.
Bactericidal activity of zinc methacrylate-salicylate obtained as described in Example 3 and zinc methacrylate-sulfosalicylate obtained as described in Example 4 is determined according to the known method (RU 2378363, C12N 1/00, C12Q 1/00, 2010) based on the exposure of a bacterial culture in a solution of bactericidal substance for a certain period of time followed by its neutralization and inoculation of the culture on a solid nutrient medium. The sensitivity of microorganisms to a disinfectant is judged by microorganism growth on the nutrient medium up to 300 CFU/ml (CFU—colony-forming unit): in particular, growth up to 100 CFU/ml exhibits incomplete bactericidal effect, growth up to 100-300 CFU/ml—sub-bactericidal effect and growth up to more than 300 CFU/ml exhibits resistance of microorganisms to a disinfectant. The determination is performed on E. coli No. 906 and S. aureus No. 1257 test strains being usually used to study the bactericidal activity of biocides as well as on clinical strains—P. aeruginosa and methicillin-resistant strain S. aureus—at salt concentrations from 0.5 to 2% and time of exposure from 5 to 60 min. Test results are given in Table 2. It follows from Table 2 that zinc methacrylate-salicylate at concentration of 1.0% exhibits stable bactericidal effect against all strains at time of exposure from 30 min. At concentration of 2.0%, it exhibits the same bactericidal effect at time of exposure from 5 min. Zinc methacrylate-sulfosalicylate at concentration of 1.0% also exhibits stable bactericidal effect against three of four investigated strains at time of exposure from 30 min.
The same method as described in Example 9 is used to determine the bactericidal activity of ZMA against three of four strains studied in Example 9. Test results are given in Table 3. From Table 3 it follows that the bactericidal activity of ZMA is substantially lower than that of the proposed salts: it exhibits stable bactericidal activity against E. coli No. 906 at time of exposure of 30 min. and concentration from 1.0 to 2.5%, not completely stable bactericidal activity against P. aeruginosa—only at concentration from 2.5%, and sub-bactericidal activity against S. aureus No. 1257—only at concentration of 2.5% and time of exposure of 60 min.
The fungicidal activity of the proposed salts is determined according to GOST 30028.4-2006 by testing samples of various materials treated with these salts for resistance to fungal spores. Test results in terms of tolerance time (in days) are given in Table 4 wherein tolerance time for untreated and ZMA-treated materials are given for comparison. It follows from Table 4 that the fungicidal activity of the proposed salts exceeds the fungicidal activity of ZMA.
The present invention can be used for production of biocides intended, for example, for incorporation into polymer materials, disinfectant and antiseptic compositions, treatment of wood, paper, building structures and other materials to prevent their damage caused by biological matters (microorganisms, fungi, algae), manufacture of various articles with biocidal properties, etc.
E. coli 1257
S. aureus 906
P. aeruginosa
S. aureus
E. coli 906
S. aureus 1257
P. aeruginosa
S. aureus
E. coli 1257
S. aureus 906
P. aeruginosa
This Application is a Continuation application of International Application PCT/RU2013/000884, filed on Oct. 8, 2013, which is incorporated herein by reference in its entirety.
| Number | Name | Date | Kind |
|---|---|---|---|
| 4258090 | Moraru | Mar 1981 | A |
| 4670492 | Nakahara | Jun 1987 | A |
| 5185033 | Hani et al. | Feb 1993 | A |
| 5298061 | Waldron et al. | Mar 1994 | A |
| 5460644 | Thomassen | Oct 1995 | A |
| 5540954 | Nicholas et al. | Jul 1996 | A |
| 5717007 | Cambon | Feb 1998 | A |
| 6399560 | Kwon et al. | Jun 2002 | B1 |
| 6858658 | Tomasgaard et al. | Feb 2005 | B2 |
| 7410553 | Blanpied et al. | Aug 2008 | B2 |
| 20080219944 | Longo et al. | Sep 2008 | A1 |
| 20090223408 | Richardson et al. | Sep 2009 | A1 |
| Number | Date | Country |
|---|---|---|
| 1511909 | Jul 2004 | CN |
| 102167775 | Aug 2011 | CN |
| 2161316 | Mar 2010 | EP |
| 2360214 | Aug 2011 | EP |
| 48040909 | Dec 1973 | JP |
| 95102413 | Mar 1997 | RU |
| 2111993 | May 1998 | RU |
| 2162870 | Feb 2001 | RU |
| 2169163 | Jun 2001 | RU |
| 2278515 | Jun 2006 | RU |
| 2315793 | Jan 2008 | RU |
| 2318942 | Mar 2008 | RU |
| 2377121 | Dec 2009 | RU |
| 2378363 | Jan 2010 | RU |
| 2395548 | Jul 2010 | RU |
| 2398804 | Sep 2010 | RU |
| 2415168 | Mar 2011 | RU |
| 2497857 | Nov 2013 | RU |
| Entry |
|---|
| International Search Report from International Application No. PCT/RU2013/000884, filed Oct. 8, 2013, dated Jul. 16, 2014. |
| Number | Date | Country | |
|---|---|---|---|
| 20160214931 A1 | Jul 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/RU2013/000884 | Oct 2013 | US |
| Child | 15088588 | US |
