Patent application number | Description | Published |
20120011749 | DEVICE ATTACHABLE TO ITEM OF CLOTHING FOR DISPENSING MATERIAL FOR ENHANCING GRIPPING PROPERTIES OF SHOE SOLE - A wiping device may be a friable layer or an absorbent pad made of a material that can absorb and retain a fluid composition and can be attached or is attached to an item of clothing, such as a sock, shoe, compression sleeve, etc. The device is impregnated with an adhesive-type tacky substance that is released when a shoe sole is wiped against it to clean the shoe sole and allow surface dust and debris to be removed from the shoe sole. The deposited substance also forms a film or coating that remains adhered to the surface of the shoe sole to improve traction by imparting tackiness to the shoe sole. | 01-19-2012 |
20120066938 | SHOE SOLES FOR ENHANCING GRIPPING WITH A SMOOTH HARD SURFACE - Shoe soles with and without removable/replaceable gripping pods for athletic or sport shoes are provided with enhanced traction. The sole portions or gripping pods may be provided with a supply of a substance that exhibits a tackiness for enhancing friction between the shoe sole and the any hard floor. The tackiness-enhancing substance may be time-released or discharged from within the shoe sole onto the lower surface(s) of the sole that make(s) contact with the smooth hard playing surface or may be in response to compression or shear forces acting on the sole during play to prolong the tacky properties and reduce slippage. A visual indicator may be provided for notifying the player that it is time to replace the worn or used pod and insert a fresh pod or insert into the pod(s) to maintain high levels of gripping. | 03-22-2012 |
20150112023 | IN-SITU ALKYLPHENOL-ALDEHYDE RESINS - The invention relates to an in-situ process for preparing an alkylphenol-aldehyde resin. The process comprises the step of providing a raw alkylphenol composition. The raw alkylphenol composition comprises one or more alkylphenol compounds and at least about 1 wt % phenol. Each alkylphenol compound has one or more alkyl substituents. The raw alkylphenol composition is reacted directly, without pre-purification, with one or more aldehydes to form an in-situ alkylphenol-aldehyde resin. The invention also relates to an in-situ alkylphenol-aldehyde resin formed from the in-situ process, and its use in a tackifier composition and rubber composition. The tackifier composition and rubber composition containing the in-situ alkylphenol-aldehyde resin show, inter alia, improved tack performance. | 04-23-2015 |
20150112024 | MODIFIED ALKYLPHENOL-ALDEHYDE RESINS STABILIZED BY A SALICYLIC ACID - The invention relates to a process for improving the stability of a base-modified alkylphenol-aldehyde resin (such as an amine-modified alkylphenol-aldehyde resin). The process comprises the step of reacting a base-modified alkylphenol-aldehyde resin with a salicylic acid to stabilize the base-modified alkylphenol-aldehyde resin. The invention also relates to a modified alkylphenol-aldehyde resin formed from the stabilizing process, and its use in a tackifier composition and rubber composition. | 04-23-2015 |
20150322193 | MODIFIED PHENOLIC RESINS AND METHODS OF MAKING AND USING THE SAME AS REINFORCING RESINS - This invention relates to processes for preparing novolak resins and using the same as reinforcing resins. One process comprises reacting one or more alkylphenols with an aldehyde in the presence of a base to form a resole resin, wherein for each mole of alkylphenol at least 1.5 moles of aldehyde are reacted; and reacting the resole resin with one or more phenolic compounds in the presence of an acidic catalyst to form a novolac resin, wherein for each mole of alkylphenol at least 1.5 moles of the phenolic compounds are reacted. Another process comprises reacting one or more alkylphenols with an aldehyde in the presence of a base to form a resole resin, and reacting the resole resin with one or more phenolic compounds under an elevated temperature to form a novolac resin. | 11-12-2015 |
20160024337 | Coating Compositions Having Hydroxyl Phenyl Functional Polymers - Coating compositions are disclosed. In some embodiments, the coating compositions are used to coat substrates such as packaging materials and the like for the storage of food and beverages. The coating compositions can be prepared from a hydroxyl phenyl functional polymer, a phenolic crosslinker, and a non-aqueous solvent, wherein the hydroxyl phenyl functional polymer is prepared using a phenol stearic acid compound, and wherein the acid number of the hydroxyl phenyl functional polymer is less than about 30 mg KOH/resin. | 01-28-2016 |
20160032040 | Acrylic Grafted Polyether Resins Based on Phenol Steric Acid and Coating Compositions Formed Therefrom - Coating compositions can be prepared from an acrylic grafted polyether resin, wherein the smallest difunctional hydroxyl phenyl segment used to form the acrylic grafted polyether resin has a molecular weight greater than about 500, and wherein the smallest difunctional hydroxyl phenyl segment used to form the acrylic grafted polyether resin does not comprise two or more non-impaired hydroxyl groups attached to two or more different five-membered or six-membered carbon atom rings in a segment having a molecular weight less than about 500. The acrylic grafted polyether resin can be prepared by reacting a dihydroxyl compound and/or a diamine compound with a phenol stearic acid compound to produce a diphenol, reacting the diphenol with a diglycidyl ether compound to form a polyether resin, and mixing the polyether resin with an ethylenically unsaturated monomer component in the presence of an initiator to form the acrylic grafted polyether resin. | 02-04-2016 |
20160032048 | Bisphenol-A Free Polyether Resins Based on Phenol Stearic Acid and Coating Compositions Formed Therefrom - Coating compositions can be prepared from a polyether resin, wherein the smallest difunctional hydroxyl phenyl segment used to form the polyether resin has a molecular weight greater than about 500, and wherein the smallest difunctional hydroxyl phenyl segment used to form the polyether resin does not comprise two or more non-impaired hydroxyl groups attached to two or more different five-membered or six-membered carbon atom rings in a segment having a molecular weight less than about 500. The polyether resin can be prepared by reacting a dihydroxyl compound and/or a diamine compound with a phenol stearic acid compound to produce a diphenol, and reacting the diphenol with a diglycidyl ether compound to form the polyether resin. | 02-04-2016 |