Ternary mixtures of solvents and their use for removing oily substances
Abstract
Ternary mixtures, particularly suitable for removing oily substances having both an hyrogenated and fluorinated or mixed basis, essentially consisting of: (a) water; (b) terbutanol; (c) a fluoropolyoxyalkylene having hydrogenated end groups and/or hydrogenated repetitive units. Such mixtures have high flash point, are non toxic and with null depleting potential of the ozone and show a ternary diagram characterized by a wide monophasic zone, wherein the three components form limpid and stable solutions.

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9 claims: 5 independent, 4 dependent
- 1Ternary mixtures essentially formed by:(a) water;(b) terbutanol;(c) a fluoropolyoxyalkylene having hydrogenated end groups and/or hydrogenated repetitive units.
- 4Ternary mixtures according to anyone of the previous claims, wherein the three components form a sole stable phase.
- 5Ternary mixtures according to anyone of the previous claims, wherein the fluoropolyoxyalkylene is formed by repetitive units, statistically distributed along the chain, selected from:-CFZO-, -CF₂CFZO-, -CZ₂CF₂CF₂O-, wherein Z is -H or -F, Rf is -CF₃, -C₂F₅, or -C₃F₇. and by hydrogenated end groups selected from -CF₂H, -CF₂CF₂H, -CFH-CF₃, and -CFH-ORf, wherein Rf is defined as above;or perfluorinated end groups selected from -CF₃, -C₂F₅, and -C₃F₇, at least one of the end groups being hydrogenated.
- 8Ternary mixtures according to claims 6 or 7, wherein the fluoropolyoxyalkylene is selected from the following classes:(a) wherein: T₁ and T₂, equal to or different from each other, are hydrogenated groups -CF₂H, -CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrognated;X is -F or -CF₃;a, b are such numbers that the boiling temperature is comprised in the range indicated above, a/b is comprised from 5 to 15;(b) T₃-O(CF₂CF₂O)c(CF₂O)d-T₄ wherein: T₃ and T₄, equal to or different from each other, are hydrogenated groups -CF₂H or -CF₂-CF₂H, or perfluorinated groups -CF₃, -C₂F₅, at least one of the end groups being hydrogenated;c, d are such numbers that the boiling temperature is comprised in the range indicated above, c/d is comprised from 0.3 to 5;(c) wherein: T₅ and T₆, equal to or different from each other, are hydrogenated groups -CF₂H, -CF₂CF₂H, or CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, -C3F₇, at least one of the end groups being hydrognated;X is -F or -CF₃;e, f, g are such numbers that the boiling temperature is comprised in the range indicated above, e/(f+g) is comprised from 1 to 10, f/g is comprised from 1 to 10;(d) wherein: T₇ and T₈, are hydrogenated groups -CFH-CF₃ or perfluorinated groups -C₂F₅, -C3F₇, at least one of the end groups being hydrogenated;h is such a number that the boiling temperature is comprised in the range indicated above;(e) T₉-O(CZ₂CF₂CF₂O)i-T₁₀ wherein: Z₂ is -F or -H;T₉ and T₁₀, equal to or different from each other, are -CF₂H or -CF₂-CF₂H groups, or perfluorinated groups -CF₃, -C₂F₅, -C3F₇, at least one of the end groups being hydrognated;i is such a number that the boiling temperature is comprised in the range indicated above;(f) wherein: Rf is -CF₃, -C₂F₅, or -C₃F₇;T₁₁ and T₁₂, equal to or different from each other, are groups -CF₂H, -CF₂CF₂H, -CFH-ORf, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrogenated;j, k, l are such numbers that the boiling temperture is comprised in the range indicated above, k+l and j+k+l are at least equal to 2, k/(j+l) is comprised from 10⁻² to 10³;l/j is comprised from 10⁻² to 10²;(g) wherein: T₁₃ and T₁₄, equal to or different from each other, are hydrogenated groups -CF₂H, -CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrogenated;X is -F or -CF₃;m, n, o, p are such numbers that the boiling temperature is comprised in the range indicated above, m/n is comprised from 5 to 40, m/(o+p) is comprised from 2 to 50, o+p is at least 3 or is lower than p;(h) T₁₅-O(CF₂CF₂O)q(CF₂O)r(CFHO)s(CF₂CFHO)t-T₁₆ wherein: T₁₅ and T₁₆, equal to or different from each other, are hydrogenated groups -CF₂H, -CF₂-CF₂H, or perfluorinated groups -CF₃, -C₂F₅, at least one of the end groups being hydrognated;q, r, s, t are such numbers that the boiling temperature is comprised in the range indicated above, q/r is comprised from 0.5 to 2, (q+r)/(s+t) is comprised from 3 to 40, s+t is at least 3, s is lower than t;(i) wherein: T₁₇ and T₁₈, equal to or different from each other, are hydrogenated groups -CF₂H, -CF₂CF₂H, -CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrogenated;X is -F or -CF₃;u, v, w, x, y are such numbers that the boiling temperature is comprised in the range indicated above, (u+v)/w is comprised from 5 to 40, (u+v)/(x+y) is comprised from 2 to 50, x+y is at least 3, x is lower than y;
- 9Process for removing oily substances from a substrate which comprises applying on said surface a ternary mixture according to claims from 1 to 8.
Independent claims5
43 paragraphs, as filed
The present invention relates to ternary mixtures of solvents, and to their use for removing oily substances.
Chlorinated solvents, such as methylene chloride or carbon tetrachloride, or chlorofluorocarbons (CFC), in particular CFC-113 (1,1,2-trichlorotrifluoroethane), are commonly used for removing oils, greases, waxes and the like from surfaces of various kind, for instance from metal articles in precision mechanical industry.
As known, such chlorinated solvents are endowed with a high depleting potential towards the ozone present in the stratosphere. For such reason their production and their use will be in a few years restricted or banned as stipulated by some International agreements (Montreal Protocol and subsequent amendments).
Therefore, the research engagement of finding other solvents, or mixtures of solvents, not damaging to the ozone of the stratosphere, non toxic and preferably with low inflammability (high flash point), which supply at the same time performances comparable to or higher than those of the chlorinated solvents above mentioned as regards the cleaning effectiveness towards oils, greases, waxes and the like, having both a mineral and a fluorinated basis.
The solvents, or mixtures of solvents proposed to such purpose are numerous. For instance in <b>EP Patent A-575,794</b> are described mixtures formed by isopropanol, water, and a fluorinated compound of formula C<sub>w</sub>H<sub>x</sub>F<sub>y</sub>O<sub>z</sub>, wherein x < y, <maths id="math0001" num=""><math display="inline"><mrow><mtext>x+y = 2w+2</mtext></mrow></math><img file="EP0712944A2_D0001.tif" /></maths>, z = 0 or 1, having boiling point comprised from 40° to 100°C. In such mixtures having a flash point generally higher than 50°C, the amount of isopropanol is by far prevailing, around 70-80% by weight.
Other solvents, or mixuters of solvents, are described in <b>US patents US 5,273,592</b> and <b>US 5,143,652.</b>
The Applicant has unexpectedly found that it is possible to obtain mixtures formed by water, terbutanol and a fluoropolyoxyalkylene having hydrogenated end groups and/or hydrogenated repetitive units, as defined hereinafter, which are particularly suitable for removing oily substances, having both an hydrogenated and a fluorinated or mixed basis, with high flash point, non toxic, and with null depleting potential of the ozone.
Object of the present invention are therefore ternary mixtures essentially formed by: (a) water; (b) terbutanol; (c) a fluoropolyoxyalkylene having hydrogenated end groups and/or hydrogenated repetitive units.
A further object of the present invention is a process for removing oil substances from the surface of a substrate, which comprises applying on said surface a ternary mixture as defined above.
The fluoropolyoxyalkylene having hydrogenated end groups and/or hydrogenated repetitive units are known products, already described, for instance, in <b>European patent application No. 94107042.7,</b> filed on May 5, 1994 in the name of the Applicant. They are formed by repetitive units, statistically distributed along the chain, selected from: -CFZO-, -CF₂CFZO-, <chemistry id="chem0001" num="0001"><img file="EP0712944A2_D0002.tif" /></chemistry> -CZ₂CF₂CF₂O-, <chemistry id="chem0002" num="0002"><img file="EP0712944A2_D0003.tif" /></chemistry><chemistry id="chem0003" num="0003"><img file="EP0712944A2_D0004.tif" /></chemistry> wherein Z is -H or -F, R<sub>f</sub> is -CF₃, -C₂F₅, or -C₃F₇. and by hydrogenated end groups selected from -CF₂H, -CF₂CF₂H, -CFH-CF₃, and -CFH-OR<sub>f</sub>, wherein R<sub>f</sub> is defined as above; or perfluorinated end groups selected from -CF₃, -C₂F₅, and -C₃F₇, being at least one of the end groups hydrogenated.
The number average molecular weight is such that the boiling range, at the presure of 1 atm, is generally comprised from 10° to 150°C, preferably from 30° to 90°C, while the amount of hydrogenated end groups and/or hydrogenated repetitive units is such that the hydrogen content is generally higher than 100 ppm, preferably higher than 2000 ppm.
In particular, fluoropolyoxyalkylenes containing hydrogen can be selected from the following classes: <ul id="ul0001" list-style="none" compact="compact"><li>(a) <chemistry id="chem0004" num="0004"><img file="EP0712944A2_D0005.tif" /></chemistry> wherein: T₁ and T₂, equal to or different from each other, are hydrogenated groups -CF₂H, -CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrogenated; X is -F or -CF₃; a, b are integers so that the boiling temperature is comprised in the range indicated above, a/b is comprised from 5 to 15;</li><li>(b) T₃-O(CF₂CF₂O)<sub>c</sub>(CF₂O)<sub>d</sub>-T₄ wherein: T₃ and T₄, equal to or different from each other, are hydrogenated groups -CF₂H or -CF₂-CF₂H, or perfluorinated groups -CF₃, -C₂F₅, at least one of the end groups being hydrogenated; c, d are integers so that the boiling temperature is comprised in the range indicated above, c/d is comprised from 0.3 to 5;</li><li>(c) <chemistry id="chem0005" num="0005"><img file="EP0712944A2_D0006.tif" /></chemistry> wherein: T₅ and T₆, equal to or different from each other, are hydrogenated groups -CF₂H, -CF₂-CF₂H, or CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, <sub>-C</sub>3 F₇, at least one of the end groups being hydrogenated; X is -F or -CF₃; e, f, g are such numbers that the boiling temperature is comprised in the range indicated above, <maths id="math0002" num=""><math display="inline"><mrow><mtext>e/(f+g)</mtext></mrow></math><img file="EP0712944A2_D0007.tif" /></maths> is comprised from 1 to 10, f/g is comprised from 1 to 10;</li><li>(d) <chemistry id="chem0006" num="0006"><img file="EP0712944A2_D0008.tif" /></chemistry> wherein: T₇ and T₈, are hydrogenated groups -CFH-CF₃ or perfluorinated groups -C₂F₅, <sub>-C</sub>3F₇, at least one of the end grouops being hydrogenated; h is such a number that the boiling temperature is comprised in the range indicated above;</li><li>(e) T₉-O(CZ₂CF₂CF₂O)<sub>i</sub>-T₁₀ wherein: Z₂ is F or H; T₉ and T₁₀, equal to or different from each other, are -CF₂H or -CF₂-CF₂H groups, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇; at least one of the end groups being hydrognated; i is such a number that the boiling temperature is comprised in the range indicated above;</li><li>(f) <chemistry id="chem0007" num="0007"><img file="EP0712944A2_D0009.tif" /></chemistry> wherein: R<sub>f</sub> is -CF₃, -C₂F₅, or -C₃F₇; T₁₁ and T₁₂, equal to or different from each other, are groups -CF₂H, -CF₂CF₂H, -CFH-OR<sub>f</sub>, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrogenated; j, k, l are such numbers that the boiling temperture is comprised in the range indicated above, k+l and j+k+l are at least equal to 2, k/(j+l) is comprised from 10⁻² to 10³, l/j is comprised frpm 10⁻² to 10²;</li><li>(g) <chemistry id="chem0008" num="0008"><img file="EP0712944A2_D0010.tif" /></chemistry> wherein: T₁₃ and T₁₄, equal to or different from each other, are hydrogenated groups -CF₂H, -CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrogenated; X is -F or -CF₃; m, n, o, p are such numbers that the boiling temperature is comprised in the range indicated above, m/n is comprised from 5 to 40, m/(o+p) is comprised from 2 to 50, o+p is at least 3 or is lower than p;</li><li>(h) T₁₅-O(CF₂CF₂O)<sub>q</sub>(CF₂O)<sub>r</sub>(CFHO)<sub>s</sub>(CF₂CFHO)<sub>t</sub>-T₁₆ wherein: T₁₅ and T₁₆, equal to or different from each other, are hydrogenated groups -CF₂H, -CF₂-CF₂H, or perfluorinated groups -CF₃, -C₂F₅, at least one of the end groups being hydrogenated; q, r, s, t are such numbers that the boiling temperature is comprised in the range indicated above, q/r is comprised from 0.5 to 2, (q+r)/(s+t) is comprised from 3 to 40, s+t is at least 3, s is lower than t;</li><li>(i) <chemistry id="chem0009" num="0009"><img file="EP0712944A2_D0011.tif" /></chemistry> wherein: T₁₇ and T₁₈, equal to or different from each other, are hydrogenated groups -CF₂H, -CF₂CF₂H, CFH-CF₃, or perfluorinated groups -CF₃, -C₂F₅, -C₃F₇, at least one of the end groups being hydrognated; X is -F or -CF₃; u, v, w, x, y are such numbers that the boiling temperature is comprised in the range indicated above, (u+v)/w is comprised from 5 to 40, (u+v)/(x+y) is comprised from 2 to 50, x+y is at least 3, x is lower than y;</li></ul> They are products obtainable by hydrolysis and subsequent decarboxylation of the -COF groups present in the corresponding perfluoropolyoxyalkylenes, as described for instance in <b>EP patents 154,297, US 4,451,646 and US 5,091,589.</b>
The starting perfluoropolyoxyalkylenes containing -COF groups as end groups and/or along the chain are described, for instance, in <b>patents GB 1,104,482,</b> (class (a)), <b>US</b><b>3,715,378</b> (class (b)), <b>US 3,242,218</b> (classes (c) and (d)), <b>EP 148,482</b> (class (e)), <b>EP 445,738</b> (class (f)), <b>EP 244,839</b> and <b>EP 337,346</b> (classes (g), (h), (i)).
For the purpose of the present invention, monophasic mixtures are particularly preferred, i.e., those wherein the three components indefinitely form a limpid and stable solution. The breath of the existence zone of such monophase can vary even considerably as the type used of fluoropolyoxyalkylene varies, depending particularly on the boiling temperature and on the hydrogen content. It results impossible, therefore, to give composition ranges for the monophasic zone having general validity. In any case, it is sufficient for the skilled to carry out some mixing tests of the three components to locate the monophase existence zone.
For guidance only, the following general criteria can be indicated: (i) when the amount of terbutanol is higher than 30% by weight, the other two components can range within the whole range of composition, i.e., practically from 0.1 to 69.9% by weight; (ii) when the amount of terbutanol is lower than 30% by weight, the amount of fluoropolyoxyalkylene containing hydrogen is preferably lower than 10% by weight, or, alternatively, the amount of water is preferably lower than 20% by weight.
Among the ternary mixtures of the present invention, are particularly suitable for removing fluorinatd oily substances those essentially formed by: <ul id="ul0002" list-style="none" compact="compact"><li>(a) from 0.1 to 30% by weight of water;</li><li>(b) from 0.1 to 60% by weight of terbutanol;</li><li>(c) from 20 to 99.8% by weight of a fluoropolyoxyalkylene having hydrogenated end groups and/or hydrogenated repeating units.</li></ul>
On the contrary, mixtures particularly suitable for removing non fluorinated oil substances are those formed essentially by: <ul id="ul0003" list-style="none" compact="compact"><li>(a) from 0.1 to 79.9% by weight of water;</li><li>(b) from 20 to 80% by weight of terbutanol;</li><li>(c) from 0.1 to 20% by weight of a fluoropolyoxyalkylene having hydrogenated end groups and/or hydrogenated repetitive units.</li></ul>
In Figs. 1 and 2 two representations of the ternary diagram related to the mixtures object of the present invention are reported, obtained with experiments by mixing, at the temperature of 23°C, the three components in different ratios and checking the existence of only one phase (1φ) or of two phases (2φ). For the representation of such diagram fluoropolyoxyalkylene was employed containing hydrogen of Example 1 (generically indicated as CFHO in the Figures).
The ternary mixtures object of the present invention can be employed for cleaning sublayers surfaces both of inorganic and organic type, such as, metals, ceramic or glass materials, polymeric substrates, etc. The characteristics making the mixtures of the present invention particularly suitable to such purpose are, in short, the following: <ul id="ul0004" list-style="none" compact="compact"><li>(a) versatility since they result effective on various types of oils, greases, waxes and the like, having both an hydrogenated and a fluorinated or mixed basis;</li><li>(b) existence of a wide monophasic zone (1φ of Fig. 1), wherein the three components form limpid and stable solutions;</li><li>(c) null toxicity;</li><li>(d) null depleting potential of the ozone (Ozone Depleting Potential, ODP);</li><li>(e) many of them have high flash point mainly depending from the type of fluoropolyoxyalkylene;</li><li>(f) recovery easiness, since many of the oil products commonly used for lubrication, and in particular greases, are removed without dissolving, wherefore they can be separated from the mixture of solvents by means of common mechanical means (for instance by separation or by filtration), wihtout having to resort to more complex and expensive separation processes (for instance distillation).</li></ul>
By hydrogen-based oils and greases, products are meant based on mineral oils derived from petroleum, or on synthetic, semi-synthetic and emulsifiable non fluorinated oils. By oils and greases having a fluorinated basis we essentially mean the lubricants based on perfluoropolyoxyalkylenes, commercially known as Fomblin<sup>(R)</sup>, Krytox<sup>(R)</sup>, Demnum<sup>(R),</sup> etc.
The removal of the oil products can be carried out according to known techniques. For instance after having mechanically removed most of the oil and grease, the piece to be cleaned is immersed into the ternary mixture object of the present invention, or the mixture is spray-applied or by means of buffers. In case of immersion, the contact betwen the mixture and surface to be cleaned can be favoured utilizing an ultrasonic bath which allows to remove more effectively also solid polluting agents, particularly when irregular surfaces must be cleaned. After cleaning, the treated article is dried, at air or in stove at a temperature generally comprised from 40° to 140°C, preferably from 70° to 110°C.
The present invention will be now further illustrated from the following working examples, which cannot be in any way limitative for the scope of the invention itself.
<b>EXAMPLES 1-5</b>
Five monophasic mixtures H₂O/terbutanol (t-BuOH)/fluoropolyoxyalkylene containing hydrogen having the compositions reported in Table 1 were prepared. As fluoropolyoxyalkylene it was employed a product of formula: CFH-O(CF₂CF₂O)<sub>m5</sub>(CF₂O)<sub>n5</sub>-CF₂H having boiling range from 30° to 130°C, weight average molecular weight M<sub>w</sub> = 316, m₅/n₅ ratio = 1.03 (determined by ¹⁹F-NMR analysis), content in hydrogen equal to 6260 ppm (determined by ¹H-NMR analysis).
The capability of the mixtures of removing oily pproducts (de-oiling) was verified according to the following method. A drop of the oily product is deposited on the bottom of a glass crystallization vessel and the mixture in question is slowly added letting it flow along the vessel walls. The behaviour of the oil drop is observed: if this completely separates from the bottom without dissolving or completely dissolves, the test is to be considered as passed. If, on the contrary, the drop remains anchored to the bottom, or it only partially comes out and/or dissolves, the test is negative.
The de-oiling tests were carried out with the following lubricating oils: <ul id="ul0005" list-style="dash" compact="compact"><li>FINA<sup>(R)</sup> IT 11/012A oil (mixture of hydrocarbons derived from petroleum);</li><li>LEYBOLD<sup>(R)</sup> N62 oil (mineral oil utilized in vacuum systems);</li><li>ESSO UNIVOLT<sup>(R)</sup> P 60 oil (refined mineral oil utilized as dielectric fluid for transformers).</li></ul>
The results are reported in Table 1. The positive tests were distinguished between those wherein solubilization of oil (+) was noticed and those wherein separation occurred without solubilization (++).
On the mixtures of Examples 3 and 5 the flash point was also measured, acording to ASTM D-56/87 standard (by a Flash TAG Close Tester).
<u>EXAMPLES 6-7</u> (comparative)
For comparative purposes, two monophasic mixtures H₂O/isopropanol (i-PrOH)/hydrogenated fluoropolyoxyalkylene, having the compositions reported in Table 1, were prepared. The hydrogenated fluoropolyoxyalkylene is the same as in Examples 1-5. With such mixtures de-oiling tests were carried out as described above. The results are reported in Table 1.
<b>EXAMPLES 8-10</b>
(comparative)
For comparative purposes, de-oiling tests were carried out as described above with the following fluids: <ul id="ul0006" list-style="dash" compact="compact"><li>the hydrogenated fluoropolyoxyalkylene of Examples 1-5 (Example 8);</li><li>a perfluoropolyoxyalkylene Galden<sup>(R)</sup> Y, having formula: CF₃-(OCF(CF₃)CF₂)<sub>n4</sub>(OCF₂)<sub>m4</sub>-OCF₃ having n₄/m₄ = 40 and boiling range between 60° and 80°C (Example 9);</li><li>a mixture formed by 67% by weight of H₂O and 33% by weight of t-BuOH (Example 10).</li></ul>
The results are reported in Table 1. <tables id="tabl0001" num="0001"><table frame="all"><title>TABLE 1</title><tgroup cols="7" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><thead valign="top"><row rowsep="1"><entry namest="col1" nameend="col1" rowsep="0" align="center">EX.</entry><entry namest="col2" nameend="col3" rowsep="0" align="center">COMPOSITION (% by weight)</entry><entry namest="col4" nameend="col4" rowsep="0" align="center">FLASH POINT (°C)</entry><entry namest="col5" nameend="col7" align="center">DE-OILING</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col3" /><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" align="center">oil FINA<sup>(R)</sup></entry><entry namest="col6" nameend="col6" align="center">oil LEYBOLD<sup>(R)</sup></entry><entry namest="col7" nameend="col7" align="center">oil ESSO<sup>(R)</sup></entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="right">1</entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">20</entry><entry namest="col4" nameend="col4" morerows="2" rowsep="1" align="center">--</entry><entry namest="col5" nameend="col5" morerows="2" rowsep="1" align="right">(+)</entry><entry namest="col6" nameend="col6" morerows="2" rowsep="1" align="right">(++)</entry><entry namest="col7" nameend="col7" morerows="2" rowsep="1" align="right">(++)</entry></row><row><entry namest="col2" nameend="col2" align="left">t-BuOH</entry><entry namest="col3" nameend="col3" align="right">60</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">20</entry></row><row><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="right">2</entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">40</entry><entry namest="col4" nameend="col4" morerows="2" rowsep="1" align="center">--</entry><entry namest="col5" nameend="col5" morerows="2" rowsep="1" align="right">(+)</entry><entry namest="col6" nameend="col6" morerows="2" rowsep="1" align="right">(++)</entry><entry namest="col7" nameend="col7" morerows="2" rowsep="1" align="right">(++)</entry></row><row><entry namest="col2" nameend="col2" align="left">t-BuOH</entry><entry namest="col3" nameend="col3" align="right">50</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">10</entry></row><row><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="right">3</entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">50</entry><entry namest="col4" nameend="col4" morerows="2" rowsep="1" align="center">18.5</entry><entry namest="col5" nameend="col5" morerows="2" rowsep="1" align="right">(++)</entry><entry namest="col6" nameend="col6" morerows="2" rowsep="1" align="right">(++)</entry><entry namest="col7" nameend="col7" morerows="2" rowsep="1" align="right">(++)</entry></row><row><entry namest="col2" nameend="col2" align="left">t-BuOH</entry><entry namest="col3" nameend="col3" align="right">45</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">5</entry></row><row><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="right">4</entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">10</entry><entry namest="col4" nameend="col4" morerows="2" rowsep="1" align="center">--</entry><entry namest="col5" nameend="col5" morerows="2" rowsep="1" align="right">(+)</entry><entry namest="col6" nameend="col6" morerows="2" rowsep="1" align="right">(++)</entry><entry namest="col7" nameend="col7" morerows="2" rowsep="1" align="right">(++)</entry></row><row><entry namest="col2" nameend="col2" align="left">t-BuOH</entry><entry namest="col3" nameend="col3" align="right">40</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">50</entry></row><row><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="right">5</entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">3</entry><entry namest="col4" nameend="col4" morerows="2" rowsep="1" align="center">> 78</entry><entry namest="col5" nameend="col5" morerows="2" rowsep="1" align="right">(+)</entry><entry namest="col6" nameend="col6" morerows="2" rowsep="1" align="right">(++)</entry><entry namest="col7" nameend="col7" morerows="2" rowsep="1" align="right">(++)</entry></row><row><entry namest="col2" nameend="col2" align="left">t-BuOH</entry><entry namest="col3" nameend="col3" align="right">30</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">67</entry></row><row><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="right">6<sup>(*)</sup></entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">5</entry><entry namest="col4" nameend="col4" morerows="2" rowsep="1" align="center">--</entry><entry namest="col5" nameend="col5" morerows="2" rowsep="1" align="right">(+)</entry><entry namest="col6" nameend="col6" morerows="2" rowsep="1" align="right">(-)</entry><entry namest="col7" nameend="col7" morerows="2" rowsep="1" align="right">(-)</entry></row><row><entry namest="col2" nameend="col2" align="left">i-PrOH</entry><entry namest="col3" nameend="col3" align="right">45</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">50</entry></row><row><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="right">7<sup>(*)</sup></entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">10</entry><entry namest="col4" nameend="col4" morerows="2" rowsep="1" align="center">--</entry><entry namest="col5" nameend="col5" morerows="2" rowsep="1" align="right">(+)</entry><entry namest="col6" nameend="col6" morerows="2" rowsep="1" align="right">(-)</entry><entry namest="col7" nameend="col7" morerows="2" rowsep="1" align="right">(-)</entry></row><row><entry namest="col2" nameend="col2" align="left">i-PrOH</entry><entry namest="col3" nameend="col3" align="right">80</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">10</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="right">8<sup>(*)</sup></entry><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">100</entry><entry namest="col4" nameend="col4" align="center">--</entry><entry namest="col5" nameend="col5" align="right">(-)</entry><entry namest="col6" nameend="col6" align="right">(-)</entry><entry namest="col7" nameend="col7" align="right">(-)</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="right">9<sup>(*)</sup></entry><entry namest="col2" nameend="col2" align="left">Galden<sup>(R)</sup>Y</entry><entry namest="col3" nameend="col3" align="right">100</entry><entry namest="col4" nameend="col4" align="center">--</entry><entry namest="col5" nameend="col5" align="right">(-)</entry><entry namest="col6" nameend="col6" align="right">(-)</entry><entry namest="col7" nameend="col7" align="right">(-)</entry></row><row><entry namest="col1" nameend="col1" morerows="1" rowsep="1" align="right">10<sup>(*)</sup></entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">67</entry><entry namest="col4" nameend="col4" morerows="1" rowsep="1" align="center">--</entry><entry namest="col5" nameend="col5" morerows="1" rowsep="1" align="right">(+)</entry><entry namest="col6" nameend="col6" morerows="1" rowsep="1" align="right">(-)</entry><entry namest="col7" nameend="col7" morerows="1" rowsep="1" align="right">(-)</entry></row><row rowsep="1"><entry namest="col2" nameend="col2" align="left">t-BuOH</entry><entry namest="col3" nameend="col3" align="right">33</entry></row></tbody></tgroup><tgroup cols="7" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="22.50mm" /><colspec colnum="2" colname="col2" colwidth="22.50mm" /><colspec colnum="3" colname="col3" colwidth="22.50mm" /><colspec colnum="4" colname="col4" colwidth="22.50mm" /><colspec colnum="5" colname="col5" colwidth="22.50mm" /><colspec colnum="6" colname="col6" colwidth="22.50mm" /><colspec colnum="7" colname="col7" colwidth="22.50mm" /><tbody valign="top"><row><entry namest="col1" nameend="col7" align="justify">(*) comparative (+) removal with solublization (++) removal without solubilization (-) poor or null removal</entry></row></tbody></tgroup></table></tables>
<b>EXAMPLE 11</b>
The mixture of Example 5 was used to verify the capability of removing both mineral and fluorinated greases, according to the following method.
A known amount of grease is uniformly spread on three metal plates (AISI 316 steel). The plates are then weighed on analytical balance and subsequently put into contact with the mixture in question in an ultrasonic bath. After 10 minutes of immersion the plates are dried in stove at 120°C for 2 hours, so as to completely remove solvents, and then weighed again. The test result is expressed as percentage of removed grease. The test conditions are the following: temperature: 60°C; grease amount: 0.5 g; mixture amount: 150 ml; ultrasonic bath power: 30 Watt. The greases employed are the following: <ul id="ul0007" list-style="dash" compact="compact"><li>mineral grease FIAT TUTELA<sup>(R)</sup> MR2 (oil/lithium soap);</li><li>fluorinated grease FOMBLIN<sup>(R)</sup> RT15 (Fomblin<sup>(R)</sup>/polytetrafluoroethylene).</li></ul>
The results are reported in Table 2.
<b>EXAMPLES 12-13</b>
(comparative)
The same tests of greases removal of Example 11 were repeated with the following fluids: <ul id="ul0008" list-style="dash" compact="compact"><li>the perfluoropolyoxyalkylene Galden<sup>(R)</sup> Y of Example 9 (Example 12);</li><li>1,1,2-trichlorotrifluoroethane (CFC-113) (Example 13).</li></ul>
The results are reported in Table 2.
As it can be noted by comparing the results of Example 11 with those of Examples 12-13, the mixtures of the present invention allow to remove both hydrogenated and fluorinated greases, with an effetiveness comparable with that of CFC-113. Moreover, the mixtures of the present invention show the advantage of removing the grease without dissolving the oil composition thereof, wherefore the mixture can be recovered by simple filtration. With other fluids, the basic oil of the grease passes into the solution, while the thickening agent partly precipitates and partly remains in suspension; the obtained solution results therefore cloudy and of difficult filtration. <tables id="tabl0002" num="0002"><table frame="all"><title>TABLE 2</title><tgroup cols="6" colsep="1" rowsep="1"><colspec colnum="1" colname="col1" colwidth="26.25mm" /><colspec colnum="2" colname="col2" colwidth="26.25mm" /><colspec colnum="3" colname="col3" colwidth="26.25mm" /><colspec colnum="4" colname="col4" colwidth="26.25mm" /><colspec colnum="5" colname="col5" colwidth="26.25mm" /><colspec colnum="6" colname="col6" colwidth="26.25mm" /><thead valign="top"><row><entry namest="col1" nameend="col1" rowsep="0" align="left">EX.</entry><entry namest="col2" nameend="col3" rowsep="0" align="center">COMPOSITION (% by weight)</entry><entry namest="col4" nameend="col4" rowsep="0" align="center">BOILING TEMP. (°C)</entry><entry namest="col5" nameend="col6" align="center">REMOVAL (% by weight)</entry></row><row><entry namest="col1" nameend="col1" /><entry namest="col2" nameend="col3" /><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" align="center">mineral grease</entry><entry namest="col6" nameend="col6" align="center">fluorinated grease</entry></row></thead><tbody valign="top"><row rowsep="0"><entry namest="col1" nameend="col1" morerows="2" rowsep="1" align="left">11</entry><entry namest="col2" nameend="col2" align="left">H₂O</entry><entry namest="col3" nameend="col3" align="right">3</entry><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" /><entry namest="col6" nameend="col6" align="left">§§ 80.0</entry></row><row rowsep="0"><entry namest="col2" nameend="col2" align="left">t-BuOH</entry><entry namest="col3" nameend="col3" align="right">30</entry><entry namest="col4" nameend="col4" align="right">69</entry><entry namest="col5" nameend="col5" align="right">§§ 98.0</entry><entry namest="col6" nameend="col6" /></row><row><entry namest="col2" nameend="col2" align="left">CFHO</entry><entry namest="col3" nameend="col3" align="right">67</entry><entry namest="col4" nameend="col4" /><entry namest="col5" nameend="col5" /><entry namest="col6" nameend="col6" align="left">§§ 100.0 <sup>(°)</sup></entry></row><row><entry namest="col1" nameend="col1" align="left">12<sup>(*)</sup></entry><entry namest="col2" nameend="col2" align="left">Galden<sup>(R)</sup>Y</entry><entry namest="col3" nameend="col3" align="right">100</entry><entry namest="col4" nameend="col4" align="right">70</entry><entry namest="col5" nameend="col5" align="right">1.0</entry><entry namest="col6" nameend="col6" align="left">§ 98.4</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">13<sup>(*)</sup></entry><entry namest="col2" nameend="col2" align="left">CFC-113</entry><entry namest="col3" nameend="col3" align="right">100</entry><entry namest="col4" nameend="col4" align="right">47</entry><entry namest="col5" nameend="col5" align="right">§ 100</entry><entry namest="col6" nameend="col6" align="left">§ 99.1</entry></row></tbody></tgroup><tgroup cols="6" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="26.25mm" /><colspec colnum="2" colname="col2" colwidth="26.25mm" /><colspec colnum="3" colname="col3" colwidth="26.25mm" /><colspec colnum="4" colname="col4" colwidth="26.25mm" /><colspec colnum="5" colname="col5" colwidth="26.25mm" /><colspec colnum="6" colname="col6" colwidth="26.25mm" /><tbody valign="top"><row><entry namest="col1" nameend="col6" align="justify">(*) comparative (§) with solubilization of the basic oil (§§) without solubilization of the basic oil (°) after 15 min</entry></row></tbody></tgroup></table></tables>
21 sheets
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| Document | Relation | Office | Cited during |
|---|---|---|---|
| US6197903B1 | Cited by | United States of America | Applicant |
| EP0805199A2 | Cited by | European Patent Office (EPO) | Search report |
| US6020298A | Cited by | United States of America | Search report |
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| EP0625526A1 | Cites | European Patent Office (EPO) | Search report |
| GB1104482A | Cites | United Kingdom | Applicant |
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| EP94107042A | Cites | European Patent Office (EPO) | Applicant |
| EP94107042A | Cites | European Patent Office (EPO) | Applicant |
14 members in 7 offices
Priority claims5
| Document | Office | Kind | Date |
|---|---|---|---|
| MI942359 | Italy | A | |
| MI942359 | Italy | A | |
| MI942359 | Italy | – | |
| MI942359 | – | – | – |
| IT1994MI02359 | – | – | – |
Members14
| Document | Office | Kind | |
|---|---|---|---|
| ITMI942359D0 | Italy | D0 | |
| ITMI942359A1 | Italy | A1 | |
| EP0712944A2This record | European Patent Office (EPO) | A2 | |
| JPH08225478A | Japan | A | |
| IT1271075B | Italy | B | |
| EP0712944A3 | European Patent Office (EPO) | A3 | |
| US5654263A | United States of America | A | |
| EP0712944B1 | European Patent Office (EPO) | B1 | |
| AT183248T | Austria | T | |
| ATE183248T1 | Austria | T1 | |
| DE69511360D1 | Germany | D1 | |
| ES2136234T3 | Spain | T3 | |
| DE69511360T2 | Germany | T2 | |
| JP3939774B2 | Japan | B2 |
52 legal events, as 6 offices reported them to INPADOC
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Numbers
- Publication
- 0712944
- Publication, DOCDB
- 0712944
- Publication, EPODOC
- EP0712944
- Application
- 95117051
- Application, DOCDB
- 95117051
- Application, EPODOC
- EP19950117051
Titles3
- German
- Ternäre Lösungsmittelgemische zur Beseitigung von ölhaltigen Stoffen
- English
- Ternary mixtures of solvents and their use for removing oily substances
- French
- Mélanges ternaires de solvants et leur utilisation pour l'enlèvement de produits huileux
Classification
- CPC, 4
- C11D7/261
- C11D7/28
- C11D7/5018
- C23G5/032
- IPC, 11
- C07C31 12
- C07C43 12
- B08B3 08
- C11D1 72
- C11D3 20
- C11D3 44
- C11D7 26
- C11D7 28
- C11D7 50
- C23G5 028
- C23G5 032
Designated states15
- Contracting states, 15
- Austria
- Belgium
- Switzerland
- Germany
- Denmark
- Spain
- France
- United Kingdom
- Greece
- Ireland
- Italy
- Liechtenstein
- Netherlands (Kingdom of the)
- Portugal
- Sweden