Patent Application
20170107444
This invention relates to aqueous compositions, including metalworking fluids, containing isothiazolones and tertiary amine compounds.
A fluid composition containing a 3-isothiazolone and alkanolamines is disclosed in U.S. Pub. No. 2008/0280792. This reference discloses that the 3-isothiazolone needs to be stabilized by addition of iodine-containing stabilizers or mercaptobenzothiazole. However, use of such stabilizers in fluids, including metalworking fluids, is undesirable for economic and environmental reasons. The problem addressed by this invention is to provide an improved aqueous composition containing 3-isothiazolones and alkanolamines
The present invention is directed to an aqueous composition comprising: (a) at least one 3-isothiazolone; and (b) at least one tertiary amine comprising three C2-C6 hydroxyalkyl groups, wherein at least one of said hydroxyalkyl groups has a secondary hydroxyl group.
“MIT” is 2-methyl-4-isothiazolin-3-one, also referred to by the name 2-methyl-3-isothiazolone. “CMIT” is 5-chloro-2-methyl-4-isothiazolin-3-one, also referred to by the name 5-chloro-2-methyl-3-isothiazolone. Preferably, the weight ratio of CMIT to MIT is at least 2:1, preferably at least 2.5:1. Preferably, the weight ratio of CMIT to MIT is no greater than 4:1, preferably no greater than 3.5:1. In one preferred embodiment of the invention, the CMIT:MIT ratio is about 3:1. “MBIT” is N-methyl-1,2-benzisothiazolin-3-one. “OIT” is 2-octyl-4-isothiazolin-3-one. Preferably, the 3-isothiazolone is MIT, CMIT/MIT, OIT, MBIT or a mixture thereof; preferably MIT and/or OIT.
As used herein, the following terms have the designated definitions, unless the context clearly indicates otherwise. The term “microbicide” refers to a compound capable of inhibiting the growth of or controlling the growth of microorganisms at a locus; microbicides include bactericides, fungicides and algaecides. The term “microorganism” includes, for example, fungi (such as yeast and mold), bacteria and algae. The following abbreviations are used throughout the specification: ppm=parts per million by weight (weight/weight), mL=milliliter, AI=active ingredient, i.e., total amount of isothiazolones. Unless otherwise specified, temperatures are in degrees centigrade (° C.), references to percentages are percentages by weight (wt %) and amounts and ratios are on an active ingredient basis, unless otherwise specified. When experiments are described as being carried out at “room temperature” this means a temperature from 20-25° C.
Aqueous compositions include, e.g., metalworking fluids and concentrates, household products (e.g., cleaners), personal care products (e.g., cream, lotions, hair care products), aqueous coatings compositions (e.g., latex paints), wood treatment compositions and fabric treatment compositions. Preferably, the aqueous composition is a metalworking fluid or a metalworking fluid concentrate. Typically concentrates are diluted for use as metalworking fluids. Preferably, the concentration of an ingredient (other than water) in the concentrate is from 10 to 100, preferably 10 to 25 times the concentration of the same ingredient in the metalworking fluid. The aqueous composition may also contain one or more metalworking additives, which include, e.g., amines other than the tertiary amines described herein, fatty acids, surfactants, soluble oils, emulsifiable oils, oiliness agents (to increase film strength e.g., polyol esters), synthetic lubricants (to improve lubricity of fluid e.g., ethylene oxide-propylene oxide random or copolymers, oil soluble polyalkylene ethers), emulsifiers (to improve wetting or dispersing of oil in water e.g., fatty amides, salts of fatty acids, nonionic surfactants), extreme pressure agents (for lubrication under high pressure e.g., sulfurized fatty materials, chlorinated paraffins, phosphorus derivatives, etc.), coupling agents (to improve the solubility of the various additives in the MWF e.g., fatty alcohols), corrosion inhibitors (to prevent part or tool corrosion e.g., amine salts of carboxylic acids, or boric acid), defoamers (to reduce foam e.g., long chain fatty alcohols, silicones, siloxanes), metal passivators (protection of newly exposed metal from corrosion e.g., triazoles), anti-mist additives (alkylphenol alkoxylates) and chelators (to reduce hard water effects, e.g., EDTA, phosphates, polyphosphates).
The hydroxyalkyl groups in the tertiary amine may be the same or different. Preferably, two of the hydroxyalkyl groups have a secondary hydroxyl group. Preferably, the tertiary amine has three C2-C5 hydroxyalkyl groups, preferably three C2-C4 hydroxyalkyl groups, preferably three hydroxyalkyl groups each of which is a C2 or C4 hydroxyalkyl group. Preferably, C2 hydroxyalkyl groups are 2-hydroxyethyl groups. Preferably, C3 hydroxyalkyl groups are 2-hydroxy-1-propyl groups. Preferably, C4 hydroxyalkyl groups are 2-hydroxy-1-butyl groups. Especially preferred amines include N,N-bis(2-hydroxybutyl)-2-aminoethanol, 1-[bis(2-hydroxyethyl)amino]-2-butanol and triisopropanol amine (TIPA, CAS no. 122-20-3).
Preferably, the aqueous composition contains at least 1 ppm of 3-isothiazolone(s) (on an active ingredient basis), preferably at least 3 ppm, preferably at least 5 ppm, preferably at least 10 ppm, preferably at least 50 ppm, preferably at least 100 ppm, preferably at least 500 ppm; preferably the composition contains no more than 6,000 ppm, preferably no more than 4,000 ppm, preferably no more than 3,000 ppm, preferably no more than 2,000 ppm, preferably no more than 1,000 ppm, preferably no more than 500 ppm. Preferably, the aqueous composition contains at least 0.1 wt % of tertiary amine(s), preferably at least 0.5 wt %, preferably at least 1 wt %, preferably at least 2 wt %, preferably at least 3 wt %, preferably at least 5 wt %; preferably the composition contains no more than 35 wt %, preferably no more than 30 wt %, preferably no more than 25 wt %, preferably no more than 20 wt %, preferably no more than 15 wt %, preferably no more than 10 wt %. The aqueous composition preferably contains at least 30 wt % water, preferably at least 40 wt %, preferably at least 50 wt %, preferably at least 60 wt %, preferably at least 70 wt %; preferably no more than 99 wt % water, preferably no more 97 wt %, preferably no more than 95 wt %, preferably no more than 90 wt %, preferably no more than 80 wt %.
Preferably, the aqueous composition is substantially free of bromic acid, iodic acid, periodic acid or their salts and mercaptobenzothiazole, i.e., the composition contains less than 0.05% total of these substances, preferably less than 0.01%, preferably less than 0.005%, preferably less than 0.001%.
Hydroxyl Content—Hydroxyl content was measured by derivatization of the amine alkoxylate with an excess of phthalic anhydride reagent with imidazole catalyst in pyridine solvent at 100° C. for 30 min using a procedure based on ASTM D 4274. After formation of the phthalate half ester, the unreacted phthalic anhydride was hydrolyzed and titrated with 1 N sodium hydroxide reagent using a Mettler DL-55 titrator. The half ester was quantified by the difference between the sample titration and a blank titration of the same amount of phthalic anhydride reagent completely hydrolyzed with water. The difference is expressed as hydroxyl number (mg KOH/g sample) or % OH. For the amine butoxylates (functionality=3) analyzed in this study, the molecular weight is calculated by the following formula: (3×1700)/% OH.
H-1 NMR—The amine butoxylate sample in chloroform-d was prepared in a 5 mm NMR tube. The data were collected by a PROTON experiment on a BRUKER 300 MHz NMR.
All of the alkoxylation reactions were performed in a jacketed, baffled 9 L stainless steel autoclave reactor equipped with a magnetically driven impeller, pressure transducer, jacket return line thermocouple, and redundant reactor thermocouples. Temperature control was achieved with a mixture of steam and cooling water to the reactor jacket introduced via control valves operated by the MOD-V digital control system. Butylene oxide (BO) was charged into a designated feed tank situated on a scale. BO was metered from the feed tank bottom outlet to the reactor through an automated flow control valve within the operating temperature (±5° C. of set point) and pressure (16-85 psia) constraints. These runs targeted the butoxylation of MEA with 2 BO equivalents and DEA with 1 BO equivalent.
Monoethanolamine and Diethanolamine were obtained from Aldrich. Dow butylene oxide was obtained from the Freeport Market Development Plant.
This run targeted the butoxylation (2 BO) of Monoethanolamine (MEA) without addition of catalyst (amine autocatalytic) using a 110° C. feed temperature and a 110° C. digest temperature. MEA (901.7 g) was charged to a 9 L reactor. The reactor was pressurized with nitrogen and vented (7 times) to remove atmospheric oxygen. Subsequently, the reactor was pressurized with nitrogen to 16-20 psia at ambient temperature. The reactor contents were heated with agitation at 110° C., then BO (2180 g total) was metered into the reactor over 4 hr at 110° C. resulting in an operating pressure of 30 psia. After the BO feed was complete, the reactor contents were agitated at 110° C. for an additional 10 hr (overnight) to consume unreacted oxide (digest). The reactor was cooled to approximately 100° C., then nitrogen sparged for 1 hr to remove any unreacted butylene oxide. Subsequently, the reactor was cooled to 60° C. and drained affording 3056.1 g of product. A sample of the reaction product analyzed by hydroxyl titration (25.228% OH corresponding to 202 MW or MEA+2.0BO). Proton NMR spectroscopy provided an estimated BO:MEA molar ratio of 2.1.
This run targeted the butoxylation (1 BO) of Diethanolamine (DEA) without addition of catalyst (amine autocatalytic) using a 110° C. feed temperature and a 110° C. digest temperature. DEA (1960.2 g) was charged to a 9 L reactor. The reactor was pressurized with nitrogen then vented (7 times) to remove atmospheric oxygen. Subsequently, the reactor was pressurized with nitrogen to 16-20 psia at ambient temperature. The reactor contents were heated with agitation at 110° C., then BO (1395 g total) was metered into the reactor over 2½ hr at 110° C. resulting in an operating pressure of 25-30 psia. After the BO feed was complete, the reactor contents were agitated at 110° C. for an additional 17 hr (overnight) to consume unreacted oxide (digest). The reactor was cooled to approximately 100° C., then nitrogen sparged for 1 hr to remove any unreacted butylene oxide. Subsequently, the reactor was cooled to 60° C. and drained affording 3161.4 g of product. A sample of the reaction product analyzed by hydroxyl titration (28.494% OH corresponding to 179 MW or DEA+1.0BO). Proton NMR spectroscopy provided an estimated BO:DEA molar ratio of 1.0.
Model MWF samples were prepared by weighing the components using an analytical scale.
Forty grams of each model MWF concentrate sample was made.
The 40 gram blank samples (no biocide) were prepared as follows:
NaOH was used to bring the final pH to 9.95-10.
The following amines were used to make up the samples:
A. 1-[bis(hydroxyl ethyl)amino]-2-butanol
B. 8-methylnonylamine diethoxylated with average 5 EO units
C. bis(2-hydroxyethyl)isodecyloxypropylamine
D. N,N-bis(2-hydroxy butyl)-2-amino ethanol
E. triethanolamine
F. 2-aminoethanol
G. TIPA
H. 3-amino-4-octanol
I. AMP 95 (2-amino-2-methylpropan-1-ol)
To prepare the dosed biocide samples, the amount of dH2O was adjusted to compensate for the biocide added. NaOH was used to bring the pH to 9.95-10 prior to adding active biocide. The following recipes were used:
The MWF samples dosed with biocide were analyzed for active level by high pressure liquid chromatography (HPLC) at time 0. The samples were then vortexed and split into a sample that was aged at room temperature and a sample that was aged at 40° C. Each week an aliquot of the aged samples was evaluated by HPLC for the level of active remaining. Samples where no active was found for two consecutive weeks were no longer analyzed. The following tables display the results for each amine with each tested biocide as wt % of remaining active ingredient at the indicated time. Bold values represent acceptable levels of stability. Amines A, D and G are within the scope of claim 1; the others are comparative.
99
90
88
96
98
102
92
84
100
92
84
100
93
92
84
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87
94
91
99
88
97
84
100
90
98
89
99
90
99
89
90
85
89
88
89
84
89
133
86
81
86
93
91
87
90
94
92
80
91
95
94
85
92
89
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87
97
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86
98
90
96
82
95
89
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86
95
82
95
80
94
86
95
90
100
86
87
87
85
86
86
83
81
82
93
83
81
87
82
87
83
117
114
107
103
82
118
109
97
96
These results demonstrate that, even at extremely high ratios of amine:isothiazolone, amines A, D and G provide much better stability both at room temperature and at 40° C. than other amines
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108
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105
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108
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110
107
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108
105
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105
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105
109
110
108
100
126
100
100
100
100
100
137
100
100
100
89
100
99
122
102
105
106
91
100
91
99
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102
115
132
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126
121
147
131
128
122
95
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100
104
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100
108
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102
98
91
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81
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86
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80
82
102
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91
102
82
96
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90
101
82
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90
98
85
98
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89
99
84
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88
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99
100
87
102
102
101
86
102
102
104
85
98
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100
81
96
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100
100
101
90
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100
87
98
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100
83
97
98
101
82
98
98
105
80
97
97
108
90
97
106
92
103
100
107
107
103
102
101
88
88
88
99
98
93
91
102
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102
98
101
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102
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100
95
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92
83
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86
104
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97
89
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84
98
95
94
94
101
98
96
95
90
85
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US15/28796 | 5/1/2015 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 61994194 | May 2014 | US |
