Aqueous dispersion of hydrophobic particles and films produced thereby
Abstract
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12 claims: 12 independent, 0 dependent
- 1An aqueous dispersion comprising:a) a particulate solid material having a hydrophobic outer surface, the particulate solid material being selected from the group consisting of calcium carbonate, kaolin and pyrophyllite;b) up to 30% by volume of an alcohol enabling said particulate solid material to form a dispersion in water and to retain the hydrophobic outer surface upon drying;andc) water. Dispersion aqueuse comprenant : a) un solide particulaire ayant une surface extérieure hydrophobe, le solide particulaire étant choisi au sein du groupe constitué du carbonate de calcium, du kaolin et de la pyrophyllite ;b) jusqu'à 30 % en volume d'un alcool permettant audit solide particulaire de former une dispersion dans l'eau et de conserver la surface externe hydrophobe après séchage ;etc) de l'eau. Wässrige Dispersion, die umfasst: a) ein teilchenförmiges Feststoffmaterial mit einer hydrophoben äußeren Oberfläche, das ausgewählt ist aus der Gruppe, die besteht aus Calciumcarbonat, Kaolin und Pyrophyllit;b) bis zu 30 Vol.-% eines Alkohols, der das teilchenförmige Feststoffmaterial in die Lage versetzt, in Wasser eine Dispersion zu bilden und die hydrophobe äußere Oberfläche beim Trocknen aufrechtzuerhalten, undc) Wasser.
- 2Dispersion aqueuse selon la revendication 1, dans laquelle le solide particulaire a une taille moyenne de particules inférieure à 3 microns. The aqueous dispersion of claim 1 wherein the particulate solid material has a median particle size below 3 microns. Wässrige Dispersion nach Anspruch 1, worin das teilchenförmige Feststoffmaterial eine mittlere Teilchengröße von < 3 µm hat.
- 3Dispersion aqueuse selon la revendication 1, dans laquelle le solide particulaire a une distribution de taille de particules dans laquelle jusqu'à 90 % des particules ont une taille de particules inférieure à 10 microns. The aqueous dispersion of claim 1 wherein the particulate solid material has a particle size distribution wherein up to 90% of the particles have a particle size of under 10 microns. Wässrige Dispersion nach Anspruch 1, worin das teilchenförmige Feststoffmaterial eine Teilchengrößenverteilung hat, bei der bis zu 90 % der Teilchen eine Teilchengröße von < 10 µm haben.
- 4Dispersion aqueuse selon la revendication 1, dans laquelle le solide particulaire comprend un noyau non hydrophobe et une surface extérieure hydrophobe. The aqueous dispersion of claim 1 wherein the particulate solid material comprises a non-hydrophobic core and a hydrophobic outer surface. Wässrige Dispersion nach Anspruch 1, worin das teilchenförmige Feststoffmaterial einen nicht-hydrophoben Kern und eine hydrophobe äußere Oberfläche aufweist.
- 5A method of forming a hydrophobic continuous film on a substrate comprising:a) adding a particulate solid material having a hydrophobic outer surface to an amount of a low boiling organic liquid sufficient to form a slurry, the particulate solid material being selected from the group consisting of calcium carbonate, kaolin and pyrophyllite;b) adding said slurry to water to form aqueous dispersion of said particulate solid material;c) applying said aqueous dispersion to the substrate;andd) enabling the aqueous dispersion to dry whereby a continuous hydrophobic film of said particulate sold material is formed on the substrate. Procédé de formation d'un film hydrophobe continu sur un substrat comprenant les étapes consistant à : a) ajouter un solide particulaire ayant une surface hydrophobe extérieure à une quantité de liquide organique, légèrement en ébullition, suffisante pour former une pâte, le solide particulaire étant choisi au sein du groupe constitué du carbonate de calcium, du kaolin et de la pyrophyllite ;b) ajouter ladite pâte à l'eau pour former une dispersion aqueuse dudit solide particulaire ;c) appliquer ladite dispersion aqueuse au substrat ;etd) permettre à la dispersion aqueuse de sécher, moyennant quoi un film hydrophobe continu dudit matériel particulaire est formé sur le substrat. Verfahren zur Bildung eines kontinuierlichen hydrophoben Films auf einem Substrat, das umfasst: a) die Zugabe eines teilchenförmigen Feststoffmaterials mit einer hydrophoben äußeren Oberfläche zu einer niedrig siedenden organischen Flüssigkeit in einer Menge, die ausreicht zur Bildung einer Aufschlämmung, wobei das teilchenförmige Feststoffmaterial ausgewählt wird aus der Gruppe, die besteht aus Calciumcarbonat, Kaolin und Pyrophyllit;b) die Zugabe der Aufschlämmung zu Wasser zur Bildung einer wässrigen Dispersion des teilchenförmigen Feststoffmaterials;c) das Aufbringen der wässrigen Dispersion auf das Substrat undd) das Trocknenlassen der wässrigen Dispersion zur Bildung eines kontinuierlichen hydrophoben Films aus dem teilchenförmigen Feststoffmaterial auf dem Substrat.
- 6Procédé selon la revendication 5, dans lequel la quantité de liquide organique légèrement en ébullition est inférieure à 30 % en volume de la dispersion aqueuse. The method of claim 5 wherein the amount of the low boiling organic liquid is up to 30 volume % of the aqueous dispersion. Verfahren nach Anspruch 5, worin die Menge der niedrig siedenden organischen Flüssigkeit bis zu 30 Vol.-% der wässrigen Dispersion ausmacht.
- 7Procédé selon la revendication 5, dans lequel l'étape (d) consiste à faire évaporer la dispersion aqueuse. The method of claim 5 wherein step (d) comprises evaporating the aqueous dispersion. Verfahren nach Anspruch 5, worin die Stufe (d) das Eindampfen der wässrigen Dispersion umfasst.
- 8Procédé selon la revendication 5, dans lequel le liquide organique légèrement en ébullition possède de 1 à 6 atomes de carbone. The method of claim 5 wherein the low boiling organic liquid has from 1 to 6 carbon atoms. Verfahren nach Anspruch 5, worin die niedrig siedende organische Flüssigkeit 1 bis 6 Kohlenstoffatome aufweist.
- 9Procédé selon la revendication 8, dans lequel le liquide organique légèrement en ébullition est choisi au sein du groupe constitué des alcools, des cétones, des éthers cycliques et de combinaisons de ceux-ci. The method of claim 8 wherein the low boiling organic liquid is selected from the group consisting of alcohols, ketones, cyclic ethers, and combinations thereof. Verfahren nach Anspruch 8, worin die niedrig siedende organische Flüssigkeit ausgewählt wird aus der Gruppe, die besteht aus Alkoholen, Ketonen, cyclischen Ethern und Kombinationen davon.
- 10Procédé selon la revendication 9, dans lequel le liquide organique légèrement en ébullition est du méthanol. The method of claim 9 wherein the low boiling organic liquid is methanol. Verfahren nach Anspruch 9, worin die niedrig siedende organische Flüssigkeit Methanol ist.
- 11Procédé selon la revendication 5, dans lequel le substrat est choisi au sein du groupe constitué de plantes cultivées, d'arbres, de plantes, de bois de sciage, de béton, de sol, de matières textiles et de produits chimiques organiques solides. The method of claim 5 wherein the substrate is selected from the group consisting of agricultural crops, trees, plants, lumber, concrete, soil, textiles and solid organic chemicals. Verfahren nach Anspruch 5, worin das Substrat ausgewählt wird aus der Gruppe, die besteht aus landwirtschaftlichen Kulturpflanzen, anderen Pflanzen, Bäumen, Nutzholz, Beton, Erde, Textilien und festen organischen Chemikalien.
- 12Procédé selon la revendication 5, comprenant l'ajout d'un solide particulaire comprenant un noyau non hydrophobe et une surface extérieure hydrophobe audit liquide organique légèrement en ébullition. The method of Claim 5 comprising adding a particulate solid material comprising a non-hydrophobic core and a hydrophobic outer surface to said low boiling organic liquid. Verfahren nach Anspruch 5, das umfasst die Zugabe eines teilchenförmigen Feststoffmaterials, das einen nicht-hydrophoben Kern und eine hydrophobe äußere Oberfläche umfasst, zu der niedrig siedenden organischen Flüssigkeit.
Independent claims12
50 paragraphs, as filed
<u>Field of the Invention</u>
The present invention is directed to an aqueous dispersion of a particulate solid having a hydrophobic outer surface which is suitable for applying to a substrate to form a continuous hydrophobic film thereon. The film applications of the present invention include coating surfaces to make them water resistant.
<u>Background of the Invention</u>
The prior art has recognized the utility of inert particulate solids as insecticides, see for example; Driggers, B.F., "Experiments with Talc and Other Dusts Used Against Recently Hatched Larvae of the Oriental and Codling Moths", <u>J. Econ. Ent. 22</u> 327-334 (1929); Hunt, C.R., "Toxicity of Insecticide Dust Diluents and Carriers to Larvae of the Mexican Bean Beetle", <u>J. Econ. Ent. 40</u> 215-219 (1947); and US patent 3,159,536 (1964).
These references all describe applying particulate solids to foliage or insects by dry dusting. Although dry dusting is useful for laboratory experimentation it is not applicable for large scale agricultural use. The use of dry dusting has declined because the extremely fine particles, usually on the order of less than 30 um, with a median particle size typically between 0.5 to 3.0 um, are prone to drift and therefore have high negative environmental impact. Dry particles also do not adhere well to the target substrate (e.g. plants). Typically only 10% to 20% of the dry dust is deposited onto the target. <u>(Pesticide Application Methods</u> by G.A. Mathews Longman Scientific & Technical, Second Ed. (1992).)
US patent 2,733,160 relates to esterils made by esterifying siliceous materials. A hygroscopic coating agent is employed to induce caking of a substance, to prevent dirt from re-settling on a surface, as a bonding agent, to lubricate and to reduce the tackiness of a surface.
DE-A-2005190 relates to a process for rendering solid surfaces water-repellent by applying thereto a coating of colloidal particulate metal oxides or metalloid oxides which have been rendered strongly hydrophobic by extensive chemical reaction of the surface thereof with certain organosilicon compounds.
DE-A-2926095 relates to a powder aerosol composition which comprises a suspension of powder, an alcohol containing 1 to 7 carbon atoms and a propellant having a specific gravity lower than the specific gravity of the suspension.
JP-A-58208124 relates to a highly dispersed hydrophobic precipitated silicic acid prepared by mixing a precipitated silicic acid with silicone oil.
JP-A-48 039 382 relates to a fine silica powder in aerogel form with paraffin wax.
Hortscience vol. 32 no. 3 1997 page 467 relates to the application of hydrophobic clays to apple and pear trees. It was published after the priority date claimed by the present application.
It has also been determined that hydrophobic particulate solids can be applied to substrates as a liquid composition to form a hydrophilic coating. To this end, the particulate substances have been combined with a dispersant having a hydrophilic end and a lipophilic end and the same added to water to form an aqueous dispersion. The dispersant concentrates at an interphase between the hydrophobic substance and water with the lipophilic end of the dispersant positioned toward the hydrophobic substance and the hydrophilic end toward the water.
General classes of dispersants are divided into different groups by chemical functionality, e.g., cationic, anionic, amphoteric, nonionic. Typical examples of surfactants include soaps (carboxylate salts), sulfonates, sulfated alcohol ethoxylates, alkylphenol ethoxylates, carboxylic and polyoxyethylene esters, amines, imidazolines, and quaternary ammonium salts. Extensive lists containing hundreds of commercial dispersants are readily available (see McCutcheon's Emulsifiers & Detergents N. Amer Ed. (1995)).
The use of dispersants, however, causes the particulate hydrophobic substance to become hydrophilic and to retain this hydrophilic character after drying. Therefore, when such dispersions are placed on a substrate they will retain water. Water results in surface damage to many substrates including agricultural crops and other plants (disease), lumber (rot), concrete (freeze cracking), soil (erosion), textiles, solid chemicals such as fertilizers (leach), and the like. Accordingly, the use of dispersants for employing a dispersion of hydrophobic particulate solids for protecting surfaces has been problematical.
It would therefore be a significant advance in the art of applying hydrophobic particulate solids to a substrate to provide the substrate with a continuous film of the particulate solid while retaining a hydrophobic character. The resulting film would provide a substantial deterrent to damage due to water.
Summary of the Invention
The present invention is generally directed to an aqueous dispersion and to continuous films formed from the same in which a particulate solid having at least a hydrophobic outer surface is formed as an aqueous dispersion, thereafter coated onto a 5 substrate and formed into a continuous film while retaining its hydrophobic character.
In particular, the present invention is directed to an aqueous dispersion comprising: <ul id="ul0001" list-style="none" compact="compact"><li>a) a particulate solid having a hydrophobic outer surface, the particulate solid material being selected from the group consisting of calcium carbonate, kaolin and pyrophyllite;</li><li>b) up to 30% by volume of an alcohol enabling said particulate solid to form a dispersion in water and to retain the hydrophobic outer surface upon drying; and</li><li>c) water.</li></ul>
In another aspect of the invention, there is provided a method of forming a hydrophobic continuous film on a substrate comprising: <ul id="ul0002" list-style="none" compact="compact"><li>a) adding a particulate solid material having a hydrophobic outer surface to an amount of a low boiling organic liquid sufficient to form a slurry, the particulate solid material being selected from the group consisting of calcium carbonate, kaolin and pyrophyllite;</li><li>b) adding said slurry to water to form an aqueous dispersion of said particulate solid material;</li><li>c) applying said aqueous dispersion to the substrate;</li><li>d) enabling the aqueous dispersion to dry, for example, by evaporating the aqueous dispersion, whereby a continuous hydrophobic film of said particulate solid is formed on the substrate.</li></ul>
Detailed Description of the Invention
The finely divided hydrophobic particulate solids of the invention are rendered hydrophobic by application of an outer coating of a suitable hydrophobic wetting agent (e.g. the particulate solid has a non-hydrophobic core and a hydrophobic outer surface). Such agents are well known in the art and common examples include: chrome complexes such as Volvan® and Quilon® obtained from DuPont; organic titanates such as Tilcom® obtained from Tioxide Chemicals; organic zirconate or aluminate coupling agents obtained from Kenrich Petrochemical, Inc.; organofunctional silanes such as Silquest® products obtained from Witco or Prosil® products obtained from PCR; modified silicone fluids such as the DM-Fluids obtained from Shin Etsu; and fatty acids such as Hystrene® or Industrene® products obtained from Witco Corporation or Emersol® products obtained from Henkel Corporation (stearic acid and stearate salts are particularly effective fatty acids for rendering a particle surface hydrophobic).
Many types of finely divided particulate solids are pretreated with hydrophobic wetting agents to render their surfaces hydrophobic, so that the particles will wet out and disperse better in non-aqueous matrixes such as used in plastics, rubber, and organic coatings. Solid particulate materials suitable for use in the present invention include typical particulate solid materials that are commercially treated with hydrophobic agents and comprise minerals such as calcium carbonate, kaolin, pyrophyllite, chalk, limestone and precipitated calcium carbonate. Examples of preferred commercial solid hydrophobic particulates that are available as an article of commerce from Engelhard Corporation, Iselin, NJ are sold under the trademark Translink®.
The term "finely divided" when utilized herein means that the individual particles have a median particle size below about 10 microns and preferably below 3 microns as measured by standard sedigraphic or laser light scattering methods- Preferably, the particulate solid material has a particle size distribution wherein up to 90% of the particles have a particle size of under about 10 microns.
Alcohols useful in the aqueous dispersion of the present invention are "low boiling" (i.e. have a boiling point generally no more than 100°C), preferably contain from I to 6 carbon atoms and enable the particulate solids to remain in finely divided form without significant agglomeration. Examples of such alcohols are methanol, ethanol, propanol, i-propanol, i-butanol, and the like. Methanol is the preferred liquid. Combinations can also be employed. Preferably the amount of alcohol is from 3 to 5 volume %, more preferably from 3.5 to 4.5 volume %, of the dispersion.
The low boiling organic liquids useful in the method of the present invention preferably contain from 1 to 6 carbon atoms. The term "low boiling" as used herein shall mean organic liquids which have a boiling point generally not more than 100°C. These liquids enable the particulate solids to remain in finely divided form without significant agglomeration. Such low boiling organic liquids are exemplified by: alcohols such as methanol, ethanol, propanol, i-propanol, i-butanol, and the like, ketones such as acetone, methyl ethyl ketone and the like, and cyclic ethers such as ethylene oxide, propylene oxide and tetrahydrofuran. Combinations of the above-mentioned liquids can also be employed. Methanol is the preferred liquid.
The low boiling organic liquid is employed in an amount sufficient to form a dispersion of the solid particulate material. The amount of the low boiling organic liquid employed in the present method is typically up to about 30 volume percent of the aqueous dispersion, preferably from about 3 to 5 volume percent and most preferably from about 3.5 to 4.5 volume percent. The hydrophobic particulate solid, particularly a particulate solid material comprising a non-hydrophobic core and a hydrophobic outer surface, is preferably added to the low boiling organic liquid to form a slurry and then the slurry is diluted with water to form the aqueous dispersion. The resulting slurry retains the particles in finely divided form wherein most of the particles are dispersed to a particle size of less than 10 microns.
The method of the present invention is preferably applied to a substrate selected from the group consisting of agricultural crops, trees, plants, lumber, concrete, soil, textiles and solid organic chemicals.
The following examples are illustrative of embodiments of the invention and are not intended to limit the invention as encompassed by the claims forming part of the application.
Example 1
Three gram quantities of a hydrophobic clay (Translink® 77 manufactured by Engelhard Corporation), were separately dispersed in 2, 4, 6, 8, and 10 milliliters of methanol, respectively. The samples were then diluted with deionized water to a total volume of 100 millimeters to yield a series of slurries containing 2, 4, 6, 8, and 10% by volume of methanol, respectively.
The methanol/water slurries were allowed to set for 24 hours before glass slides, surrounded with two sided adhesive tape, were dipped into the slurries. Hydrophobicity was determined by measuring the contact angle of the resulting dried particulate films prepared from the aqueous dispersions of hydrophobic particles. As used herein the static contact angle is the equilibrium angle measured between a liquid and a solid by drawing a tangent at the point of contact. A dynamic contact angle analyzer records both advancing and receding contact angles by the Wilhelmy technique as a glass slide or another surface is moved up and down through a liquid. The relationship between wetting force and contact angle is given by the modified Youngs equation shown below:<maths id="math0001" num=""><math display="block"><mrow><mtext>F = </mtext><mtext mathvariant="italic">γp</mtext><mtext>cosθ</mtext></mrow></math><img file="EP0969718B1_D0001.tif" /></maths> where F = wetting force; y = liquid surface tension; and p = wetting perimeter
All measurements herein were made in water using either glass slides surrounded by adhesive tape or dual sided adhesive tape coated with particulate solids. Calibration of the water surface tension was made using a platinum plate.
An angle below 90 degrees is considered hydrophilic while an angle above 90 degrees is considered hydrophobic. The contact angles of the respective dried particle films were recorded with a Cahn DCA (Dynamic Contact Angle) instrument. The results are shown in the Table 1. All of the films formed in accordance with the present invention were hydrophobic and gave contact angles well above 90 degrees.
A control sample was prepared in the same manner as described above except that the methanol was omitted. Without the methanol, the hydrophobic clay floated on the water and would not wet out even with vigorous agitation.
Example 2
Three gram quantities of Translink® 77, manufactured by Engelhard Corporation, was separately dispersed into 2, 4, 6, 8, and 10 milliliters of ethanol, respectively. The samples were then diluted with deionized water to a total volume of 100 milliliters to yield a series of slurries containing 2, 4, 6, 8, and 10% by volume of ethanol, respectively. Contact angle measurements were performed as described in Example 1. The results are shown in Table 1. The contact angle for each of the ethanol containing slurries was well above 90°. Thus each of the samples produced in accordance with the present invention retained its hydrophobic character. <tables id="tabl0001" num="0001"><table frame="all"><title>TABLE 1</title><tgroup cols="3" colsep="1" rowsep="1"><colspec colnum="1" colname="col1" colwidth="52.50mm" /><colspec colnum="2" colname="col2" colwidth="52.50mm" /><colspec colnum="3" colname="col3" colwidth="52.50mm" /><thead valign="top"><row rowsep="1"><entry namest="col1" nameend="col1" align="center">% ALCOHOL</entry><entry namest="col2" nameend="col2" align="center">EXAMPLE 1 CONTACT ANGLE METHANOL</entry><entry namest="col3" nameend="col3" align="center">EXAMPLE 2 CONTACT ANGLE ETHANOL</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="center">2</entry><entry namest="col2" nameend="col2" align="center">164°</entry><entry namest="col3" nameend="col3" align="center">148°</entry></row><row><entry namest="col1" nameend="col1" align="center">4</entry><entry namest="col2" nameend="col2" align="center">151°</entry><entry namest="col3" nameend="col3" align="center">153°</entry></row><row><entry namest="col1" nameend="col1" align="center">6</entry><entry namest="col2" nameend="col2" align="center">147°</entry><entry namest="col3" nameend="col3" align="center">140°</entry></row><row><entry namest="col1" nameend="col1" align="center">8</entry><entry namest="col2" nameend="col2" align="center">130°</entry><entry namest="col3" nameend="col3" align="center">167°</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="center">10</entry><entry namest="col2" nameend="col2" align="center">155°</entry><entry namest="col3" nameend="col3" align="center">157°</entry></row></tbody></tgroup></table></tables>
Example 3
Translink® 77 was dispersed in ethanol and/or methanol-containing solutions as shown in Table 2 and then the samples were diluted with water to yield slurries containing 4% by volume of the ethanol/methanol mixture dispersion. Dried particle films were made from the dispersions at 1, 8, 24 hours and greater than 24 hours after the dispersions were prepared. The contact angle measurements were made as described in Example 1 and the results are shown in Table 2. As shown in Table 2 the contact angle for each of the slurries of the present invention was well above 90 degrees indicating that the dried particulate films were hydrophobic. The dispersions were also stable for over 24 hours. <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 rowsep="1"><entry namest="col1" nameend="col1" align="center">% METHANO L</entry><entry namest="col2" nameend="col2" align="center">% ETHANOL</entry><entry namest="col3" nameend="col3" align="center">CONTACT ANGLE 1 HR.</entry><entry namest="col4" nameend="col4" align="center">CONTACT ANGLE 8 HRS.</entry><entry namest="col5" nameend="col5" align="center">CONTACT ANGLE 24 HRS.</entry><entry namest="col6" nameend="col6" align="center">CONTACT ANGLE >24 HRS.</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="center">4</entry><entry namest="col2" nameend="col2" align="center">0</entry><entry namest="col3" nameend="col3" align="center">158°</entry><entry namest="col4" nameend="col4" align="center">156°</entry><entry namest="col5" nameend="col5" align="center">142°</entry><entry namest="col6" nameend="col6" align="center">152°</entry></row><row><entry namest="col1" nameend="col1" align="center">3</entry><entry namest="col2" nameend="col2" align="center">1</entry><entry namest="col3" nameend="col3" align="center">138°</entry><entry namest="col4" nameend="col4" align="center">153°</entry><entry namest="col5" nameend="col5" align="center">139°</entry><entry namest="col6" nameend="col6" align="center">143°</entry></row><row><entry namest="col1" nameend="col1" align="center">2</entry><entry namest="col2" nameend="col2" align="center">2</entry><entry namest="col3" nameend="col3" align="center">132°</entry><entry namest="col4" nameend="col4" align="center">136°</entry><entry namest="col5" nameend="col5" align="center">154°</entry><entry namest="col6" nameend="col6" align="center">141°</entry></row><row><entry namest="col1" nameend="col1" align="center">1</entry><entry namest="col2" nameend="col2" align="center">3</entry><entry namest="col3" nameend="col3" align="center">149°</entry><entry namest="col4" nameend="col4" align="center">155°</entry><entry namest="col5" nameend="col5" align="center">157°</entry><entry namest="col6" nameend="col6" align="center">153°</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="center">0</entry><entry namest="col2" nameend="col2" align="center">4</entry><entry namest="col3" nameend="col3" align="center">158°</entry><entry namest="col4" nameend="col4" align="center">133°</entry><entry namest="col5" nameend="col5" align="center">150°</entry><entry namest="col6" nameend="col6" align="center">147°</entry></row></tbody></tgroup></table></tables>
Example 4
Four dispersions of each containing 4 grams of Translink® 77 were prepared in water under low shear mixing conditions. The first dispersion employed a 4 % concentration of methanol as the dispersant. The second dispersion was prepared in the same manner except that methanol was replaced by four drops of an alkoxylated fatty amine (Ethomeen 0/12 sold by Akzo Nobel Chemicals, Inc.) The third dispersion was prepared in the same manner except that four drops of a tall oil hydroxy ethyl imidazoline (Monazoline T sold by MONA Industries, Inc.) was used as the dispersant. The fourth dispersion was prepared in the same manner except that four drops of a propylene oxide ethylene oxide block copolymer (Pluronic L-62 sold by BASF Corporation) was used.
The particle size distribution of the resulting slurries was measured and the results are shown in Table 3. <tables id="tabl0003" num="0003"><img file="EP0969718B1_D0002.tif" /></tables>
As shown in Table 3, the aqueous dispersion formed in accordance with the present invention exhibited much finer particles than the dispersions formed by typical dispersants used in the industry. For example up to 90% of the particles in the dispersion of the present invention had a particle size of 9.1 or less while the closest comparative samples showed a particle size of 87.3 for up to 90% of the particles.
Each of the dispersions described above was sprayed onto a coated glass slide and allowed to dry. Thereafter, a drop of water was placed onto the coated glass slides. The droplet on the coated glass slide in accordance with the present invention remained beaded and did not spread out indicating that the coating was hydrophobic. Each of the water droplets on the other glass slides spread out indicating that the particle films were hydrophilic.
Example 5
Four slurries were prepared as in Example 4 except that the slurries were made under high shear conditions. In particular, the slurries were milled for 30 minutes using a Cowles high-shear blade on a Premier Mill Corporation high speed dispersator. Particle size measurements were made of the slurries and the remainder of the slurries were filtered. Contact angle measurements of the dry particles were made. The results are shown in Table 4. <tables id="tabl0004" num="0004"><img file="EP0969718B1_D0003.tif" /></tables>
As shown from the results in Table 4, many of the agglomerates were broken down under high shear conditions. However, the particles were no longer hydrophobic except for the sample employing methanol.
Example 6
The following example demonstrates the invention in an agricultural field application. In a plastic pail 100 pounds of Translink® 77 was slowly added to 16 gallons of commercial methanol under gentle agitation with a paddle. The mixture was then transferred to a recirculating spray tank and diluted to 400 gallons with water to make a slurry of 3% Translink®77 and 4% methanol in water. After five (5) minutes of mixing, the dispersion was ready to spray. A peach and apple orchard was sprayed using a Friendly® hydraulic sprayer fitted with standard fan nozzles. After spraying, the sprayed tree leaves were determined upon drying to be hydrophobic, since added water droplets were observed to bead up on the surfaces of the leaves.
Example 7
Example 6 was repeated except that methanol was replaced with a 1% Safer® Soap (sold by Safer, Incorporated) which is a potassium fatty acid commonly used as an agricultural surfactant and insecticide. The orchards were sprayed as described in Example 6. Upon drying, the tree leaves were observed to be hydrophilic since added drops of water spread out upon the surfaces of the leaves.
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| US10317129B2 | Cited by | United States of America | Applicant |
| US9914849B2 | Cited by | United States of America | Applicant |
| DE2005190A | Cites | Germany | – |
| DE2926095A | Cites | Germany | – |
| US2733160A | Cites | United States of America | – |
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| 9803966 | United States of America | W | |
| 9803966 | United States of America | W | |
| 812301 | – | – | – |
| US19970812301 | – | – | – |
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| Document | Office | Kind | |
|---|---|---|---|
| ZA981841B | South Africa | B | |
| CA2282404A1 | Canada | A1 | |
| CA2282544A1 | Canada | A1 | |
| CA2283102A1 | Canada | A1 | |
| CA2283120A1 | Canada | A1 | |
| WO9838848A1 | World Intellectual Property Organization (WIPO) | A1 | |
| WO9838855A1 | World Intellectual Property Organization (WIPO) | A1 | |
| WO9838866A1 | World Intellectual Property Organization (WIPO) | A1 | |
| WO9838867A1 | World Intellectual Property Organization (WIPO) | A1 | |
| AU6343598A | Australia | A | |
| AU6443798A | Australia | A | |
| AU6443898A | Australia | A | |
| AU6675398A | Australia | A | |
| ZA981843B | South Africa | B | |
| ZA981844B | South Africa | B | |
| US5908708A | United States of America | A | |
| PE55999A1 | Peru | A1 | |
| ZA981842B | South Africa | B | |
| PE55899A1 | Peru | A1 | |
| PE63299A1 | Peru | A1 | |
| PE63399A1 | Peru | A1 | |
| TR199902119T2 | Türkiye | T2 | |
| TR199902120T2 | Türkiye | T2 | |
| TR199902136T2 | Türkiye | T2 | |
| EP0969718A1 | European Patent Office (EPO) | A1 | |
| EP0969725A1 | European Patent Office (EPO) | A1 | |
| EP0971593A1 | European Patent Office (EPO) | A1 | |
| US6027740A | United States of America | A | |
| IN183680B | India | B | |
| NZ337203A | New Zealand | A | |
| BR9808153A | Brazil | A | |
| BR9808155A | Brazil | A | |
| CN1249663A | China | A | |
| CN1249664A | China | A | |
| IN183797B | India | B | |
| US6060521A | United States of America | A | |
| AR010126A1 | Argentina | A1 | |
| AR010127A1 | Argentina | A1 | |
| US6069112A | United States of America | A | |
| AR010405A1 | Argentina | A1 | |
| AR010406A1 | Argentina | A1 | |
| CA2352876A1 | Canada | A1 | |
| WO0032046A2 | World Intellectual Property Organization (WIPO) | A2 | |
| AU2706300A | Australia | A | |
| EP1011309A1 | European Patent Office (EPO) | A1 | |
| BR9812287A | Brazil | A | |
| NZ337205A | New Zealand | A | |
| US6110867A | United States of America | A | |
| CN1265003A | China | A | |
| PE20001045A1 | Peru | A1 | |
| WO0032046A3 | World Intellectual Property Organization (WIPO) | A3 | |
| US6156327A | United States of America | A | |
| KR20000075963A | Republic of Korea | A | |
| KR20000075964A | Republic of Korea | A | |
| KR20000075972A | Republic of Korea | A | |
| IL131472D0 | Israel | D0 | |
| IL131473D0 | Israel | D0 | |
| IL131474A | Israel | A | |
| AU731684B2 | Australia | B2 | |
| AU731843B2 | Australia | B2 | |
| CA2385060A1 | Canada | A1 | |
| WO0122803A1 | World Intellectual Property Organization (WIPO) | A1 | |
| AU7370600A | Australia | A | |
| US6235683B1 | United States of America | B1 | |
| TW445133B | Taiwan Province of China | B | |
| BR9915935A | Brazil | A | |
| JP2001513818A | Japan | A | |
| EP1139763A2 | European Patent Office (EPO) | A2 | |
| KR20010104307A | Republic of Korea | A | |
| JP2001524945A | Japan | A | |
| JP2001524946A | Japan | A | |
| TR200101545T2 | Türkiye | T2 | |
| CN1332607A | China | A | |
| NZ337204A | New Zealand | A | |
| CO5140105A1 | Colombia | A1 | |
| CO5140106A1 | Colombia | A1 | |
| CO5140107A1 | Colombia | A1 | |
| CO5140108A1 | Colombia | A1 | |
| NO20021499D0 | Norway | D0 | |
| IL143435D0 | Israel | D0 | |
| AU747461B2 | Australia | B2 | |
| JP2002515760A | Japan | A | |
| NO20021499L | Norway | L | |
| TR200200836T2 | Türkiye | T2 | |
| TR200200867T2 | Türkiye | T2 | |
| KR20020051920A | Republic of Korea | A | |
| EP1235479A1 | European Patent Office (EPO) | A1 | |
| JP2002530125A | Japan | A | |
| US6464995B1 | United States of America | B1 | |
| CN1377222A | China | A | |
| WO0122803A9 | World Intellectual Property Organization (WIPO) | A9 | |
| AR025903A1 | Argentina | A1 | |
| CO5231179A1 | Colombia | A1 | |
| NZ337202A | New Zealand | A | |
| TW529906B | Taiwan Province of China | B | |
| JP2003516120A | Japan | A | |
| EP0971593B1 | European Patent Office (EPO) | B1 | |
| AT241276T | Austria | T | |
| ATE241276T1 | Austria | T1 | |
| IL131473A | Israel | A |
50 legal events, as 6 offices reported them to INPADOC
Over the term
Point at a mark for the eventEvents
| Event | Code | Office | |
|---|---|---|---|
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Announcement of lapse in spainLapsedFD2A | FD2A | ES | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Notification of lapseLapsedST | ST | FR | |
| Nl: lapsed or anulled due to non-payment of the annual feeLapsedNLV4 | NLV4 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Gb: european patent ceased through non-payment of renewal feeCeasedGBPC | GBPC | EP | |
| Be: lapsedLapsedBERE | BERE | EP | |
| Be: lapsedLapsedBERE | BERE | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | EP | |
| Patent lapsedLapsedMM4A | MM4A | IE | |
| No opposition filedOpposition26N | 26N | EP | |
| No opposition filed within time limitOppositionORIGINAL CODE: 0009261PLBE | PLBE | EP | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: NO OPPOSITION FILED WITHIN TIME LIMITSTAA | STAA | EP | |
| Fr: translation filedET | ET | EP | |
| Definitive protectionFG2A | FG2A | ES | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Patent ceasedCeasedPL | PL | CH | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Corresponds to:REF | REF | EP | |
| European patents granted designating irelandGrantedFG4D | FG4D | IE | |
| European patent takes effect as a national patent in ch/liEP | EP | CH | |
| Designated contracting statesAK | AK | EP | |
| European patent grantedGrantedFG4D | FG4D | GB | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| (expected) grantORIGINAL CODE: 0009210GRAA | GRAA | EP | |
| Grant fee paidORIGINAL CODE: EPIDOSNIGR3GRAS | GRAS | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOS IGRAGRAH | GRAH | EP | |
| First examination report despatched17Q | 17Q | EP | |
| Request for examination filed17P | 17P | EP | |
| Designated contracting statesAK | AK | EP | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI | EP |
Numbers
- Publication
- 0969718
- Publication, DOCDB
- 0969718
- Publication, EPODOC
- EP0969718
- Application
- 98908810
- Application, DOCDB
- 98908810
- Application, EPODOC
- EP19980908810
Titles3
- German
- WÄSSRIGE DISPERSIONEN HYDROPHOBER TEILCHEN UND MIT DIESEN HERGESTELLTE FILME
- English
- AQUEOUS DISPERSION OF HYDROPHOBIC PARTICLES AND FILMS PRODUCED THEREBY
- French
- SOLIDE PARTICULAIRE EN DISPERSION AQUEUSE ET A SURFACE EXTERIEURE HYDROPHOBE, ET FILMS AINSI OBTENUS
Classification
- CPC, 12
- B01J13/00
- A01G7/06
- A01G7/00
- A01N25/04
- A01N25/26
- A01N59/06
- Y10S424/10
- Y10S47/11
- Y10T428/662
- Y02A50/30
- A01G9/20
- C09D5/006
- IPC, 7
- A01G7 00
- A01N25 04
- A01N25 26
- A01N59 00
- A01N59 06
- B01J13 00
- C09D17 00
Designated states18
- Contracting states, 18
- Austria
- Belgium
- Switzerland
- Germany
- Denmark
- Spain
- Finland
- France
- United Kingdom
- Greece
- Ireland
- Italy
- Liechtenstein
- Luxembourg
- Monaco
- Netherlands (Kingdom of the)
- Portugal
- Sweden