This disclosure relates to urethane foam for use in impregnating cosmetic composition.
In the old days, cosmetic compositions were used mainly indoors. However, as leisure activities have been generalized recently and modern life styles have been changed correspondingly, cosmetic compositions have been frequently used outdoors. Particularly, in the old days, UV protecting cosmetic compositions were used mostly in summer seasons. However, as modern people enjoy outdoor activities and recognize hazard of UV rays more and more, there is a tendency for UV protecting cosmetic compositions to be used frequently throughout all the seasons besides summer seasons. Therefore, there is an increasing need for cosmetic compositions convenient to use and easy to carry.
Polyester-based urethane foam was developed accidentally by a German technical specialist in the late 1940's during which development of plastics was in the midst. Since such urethane foam is based on polyester, it is also called ester foam. Producing such urethane foam requires no advanced technology. Thus, polyester-based urethane foam has been produced generally and used in various industrial fields, particularly those requiring strong tensile force.
However, polyester-based urethane foam tends to be broken easily under a wet environment. In addition, it has a microcellular structure and low air permeability, and thus shows low cushiony feel, softness and flexibility. As a result, polyester-based urethane foam is not suitable for use in impregnating a cosmetic composition, particularly a liquid cosmetic composition. Under these circumstances, there is an imminent need for developing urethane foam suitable for use in impregnating a cosmetic composition.
This disclosure is directed to providing urethane foam for use in impregnating a cosmetic composition, the urethane foam being capable of maintaining high stability of the cosmetic composition to be impregnated therein and high post-impregnation stability.
In one general aspect, there is provided polyether-based urethane foam for use in impregnating a cosmetic composition.
The polyether-based urethane foam disclosed herein maintains high stability even after carrying out impregnation with a cosmetic composition, and improves portability and touch feel of a cosmetic composition.
In one aspect, there is provided polyether-based urethane foam for use in impregnating a cosmetic composition. In another aspect, the polyether-based urethane foam may function as a carrier in which a cosmetic composition is supported and retained.
As used herein, the term ‘urethane foam’ means a foamed and solidified polyurethane resin, and is also referred to as ‘foamed urethane’.
In one aspect, the polyether-based urethane foam is more resistant against humidity as compared to polyester-based urethane foam, and thus is not broken easily under a high-humidity condition and shows high stability. In addition, the polyether-based urethane foam has a larger cellular structure than polyester-based urethane foam, and thus has improved air permeability, cushiony feel, softness and flexibility. Further, the polyether-based urethane foam requires reduced cost for production, and thus has higher cost-efficiency than polyester-based urethane foam.
In one aspect, urethane foam may include dry urethane foam or wet urethane foam. Particularly, wet polyether-based urethane foam has the properties as shown in the following Table 1.
In general, wet polyether-based urethane foam has a smaller pore size and more dense structure than dry polyether-based urethane foam. While dry polyether-based urethane foam has oleophilic surface properties, wet polyether-based urethane foam has hydrophilic surface properties as a result of wet foaming. Wet polyether-based urethane foam is continuous microporous urethane foam having uniform and high porosity, shows high water/oil absorbability, and produces no particles spontaneously.
In one aspect, urethane foam may have a quenched or reticulated structure. In another aspect, urethane foam may have a reticulated structure that allows uniform and easy impregnation with a cosmetic composition and provides a high impregnation ratio.
In one aspect, urethane foam may have a density of 1 to 3 pounds per cubic feet (pcf), particularly 1 to 2 pcf. When urethane foam has a density less than 1 pcf, a cosmetic composition may be liberated excessively and thus is not convenient to use. When urethane foam has a density higher than 3 pcf, it is not possible to provide a sufficient number of pores through which a cosmetic composition is impregnated, thereby making it difficult to impregnate a cosmetic composition effectively.
In one aspect, urethane foam may have a pore number of 70 to 120 pores per inch (ppi), particularly 75 to 95 ppi. When urethane foam has a pore number less than 70 ppi, it has poor elasticity, is not convenient to use and is not amenable to control of the flowability of a cosmetic composition. When urethane foam has a pore number greater than 120 ppi, it provides low durability and poor touch feel of a cosmetic composition during use.
In one aspect, urethane foam may have an ASKER hardness of 10 to 70, particularly 20 to 60, and more particularly 30 to 50 as measured by DUROMETER HARDNESS TESTER (Type F) available from ASKER. When urethane foam is too soft such that it has a hardness less than 10, a cosmetic composition impregnated in the urethane foam may be liberated excessively, while it is taken by cosmetic tools used for a make-up composition enclosed in a packed container, for example by nitrile butadiene rubber (NBR) puff, or hands. When urethane foam is too hard such that it has a hardness greater than 70, a cosmetic composition may not be liberated easily.
In one aspect, urethane foam may have an open cell structure. When urethane foam has a closed cell structure, air bubbles are kept in urethane so that a low-viscosity emulsion type cosmetic composition may not be impregnated therein easily. Thus, urethane foam having an open cell structure may be used specifically.
In one aspect, the cosmetic composition to be impregnated in urethane foam includes a liquid cosmetic composition, particularly an emulsion type cosmetic composition, and more particularly a water in oil (W/O) type or oil in water (O/W) type emulsion cosmetic composition.
In one aspect, the emulsion cosmetic composition may have a low viscosity, particularly of 5,000 to 15,000 centi poise (cps), and more particularly of 6,000 to 10,000 cps. When the emulsion cosmetic composition has a viscosity less than 5,000 cps, it may undergo separation into an oil phase and an aqueous phase, thereby making it difficult to impregnate urethane foam uniformly with the composition. When the emulsion cosmetic composition has a viscosity higher than 15,000 cps, it may provide an undesirably tacky and heavy touch feel while applied onto the skin.
In one aspect, the cosmetic composition includes both a skin care composition and a make-up composition. Particular non-limiting examples of the cosmetic composition may include make-up primer, make-up base, foundation, powder, twin cake, lipstick, lip gloss, eye shadow, eyebrow, concealer, lip liner, blusher, UV protecting agent, lotion, cream or essence. More particularly, the cosmetic composition may be formulated into make-up primer, make-up base, liquid or solid foundation, powder, twin cake, lipstick, lip gloss, eye shadow, eyebrow, concealer or blusher, but is not limited thereto.
In one aspect, there is provided a make-up product in which polyether-based urethane foam impregnated with a cosmetic composition is enclosed. The make-up product includes a cosmetic composition applied to the polyether-based urethane foam disclosed herein, and thus allows high-quality packing of the cosmetic composition. In addition, the make-up product allows the cosmetic composition to be supported uniformly in urethane foam for a long period of time and to be liberated in an adequate amount when users take the cosmetic composition. Further, the make-up product maintains high long-term durability and stability. The make-up product disclosed herein may be provided as a packed container, abbreviated generally as ‘pact’, which includes a container having a lower part in which polyether-based urethane foam is received, and an upper part having a lid to which a mirror or the like may be attached.
The examples, comparative examples, preparation examples and test examples will now be described. The following examples are for illustrative purposes only and not intended to limit the scope of this disclosure.
To select urethane foam suitable for impregnation with a W/O type or O/W type low-viscosity emulsion cosmetic composition, various types of urethane foam are determined for their properties. The following Tables 2 and 3 show each type of urethane foam and the corresponding properties. In addition,
In Table 3, Polyether-based urethane foam 1 is dry polyether-based urethane foam.
Among the different kinds of urethane foam listed in Tables 2 and 3, Polyether-based urethane foam 1 (Example 1), Polyester-based urethane foam 2 (Comparative Example 1) and Polyester-based urethane foam 3 (Comparative Example 2) are selected and subjected to impregnation with a W/O type emulsion make-up composition. Then, their stabilities are evaluated as a function of storage temperature and time. The results are shown in the following Table 4 and
As can be seen from the above results, when each foam is impregnated with a W/O type emulsion make-up composition, each urethane foam according to Comparative Examples 1 and 2 is broken, causes separation of the make-up composition and generates air bubbles with time under a high temperature or severe change in temperature, and thus is shown to be very unstable. On the contrary, Example 1 substantially maintains its original state and shows high stability.
Therefore, it can be seen that polyether-urethane foam shows higher stability than polyester-based urethane foam upon impregnation with a cosmetic composition, and thus is more suitable for impregnating a cosmetic composition.
In Preparation Examples 1 and 2, W/O type emulsion UV protecting cosmetic compositions are prepared according to the formulation of the following Table 5.
Particularly, a UV protecting agent is introduced to oily ingredients and dissolved and emulsified therein. Next, the oily ingredients are mixed with a surfactant and heated to and agitated at 80° C. so that the mixture is homogenized. Then, a pigment is further added thereto, followed by agitation and homogenization, to provide an oily part. In a separate mixer, aqueous ingredients are mixed and heated to and agitated at 80° C. to provide a completely dissolved aqueous part. The prepared aqueous part is introduced gradually to the oily part and subjected to emulsification by using a homogenizer mixer. After cooling to 50° C., skin protecting ingredients and fragrances are introduced thereto, followed by cooling, to provide a low-viscosity W/O type emulsion UV protecting cosmetic composition.
In Table 5, disteardimonium hectorite functions as a thickening agent, polymethyl methacrylate serves as a pure body pigment, and titanium dioxide/aluminum hydroxide/stearic acid serves as an inorganic UV protecting agent.
Different types of polyether-based urethane foam having a different value of hardness are impregnated with Preparation Examples 1 and 2, and user preference of each case is determined. Particularly, 50 females are divided into two groups (each group having 25 persons). They are allowed to apply each of Preparation Example 1 and Preparation Example 2 impregnated in polyether-based urethane foam having a different value of hardness to their skin with NBR puff for 2 days. Then, overall user preference including touch feel and coating quality is evaluated in each case. The results are shown in the following Tables 6 and 7.
As can be seen from the above results, the highest preference is available when polyether-based urethane foam used for impregnation with both compositions according to Preparation Examples 1 and 2 has Asker hardness value of 40.
Those skilled in the art will appreciate that the conceptions and specific embodiments disclosed in the foregoing description may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present disclosure. Those skilled in the art will also appreciate that such equivalent embodiments do not depart from the spirit and scope of the disclosure as set forth in the appended claims.
Number | Date | Country | Kind |
---|---|---|---|
10-2011-0026466 | Mar 2011 | KR | national |
This application is a continuation-in-part of U.S. patent application Ser. No. 14/034,650, filed on Sep. 24, 2013, which is a continuation-in-part of International Application No. PCT/KR2012/002141, filed on Mar. 23, 2012, which claims priority to Korean Patent Application No. 10-2011-0026466, filed on Mar. 24, 2011.
Number | Name | Date | Kind |
---|---|---|---|
1851462 | Steller | Oct 1932 | A |
2764565 | Hoppe et al. | Sep 1956 | A |
3133309 | Miles | May 1964 | A |
3463745 | Hofrichter et al. | Aug 1969 | A |
3465759 | Haefele | Sep 1969 | A |
3748288 | Winkler et al. | Jul 1973 | A |
4130121 | Wetzel | Dec 1978 | A |
4259452 | Yukuta et al. | Mar 1981 | A |
4309509 | Wood | Jan 1982 | A |
4323656 | Strickman et al. | Apr 1982 | A |
4344930 | MacRae et al. | Aug 1982 | A |
4374935 | Decker et al. | Feb 1983 | A |
4427798 | Konig et al. | Jan 1984 | A |
4440181 | Scherer | Apr 1984 | A |
4537912 | Griswold | Aug 1985 | A |
4594835 | Gray | Jun 1986 | A |
4656196 | Kelly et al. | Apr 1987 | A |
4706693 | Spector | Nov 1987 | A |
4806572 | Kellett | Feb 1989 | A |
4985467 | Kelly et al. | Jan 1991 | A |
5064653 | Sessions et al. | Nov 1991 | A |
5065752 | Sessions et al. | Nov 1991 | A |
5098621 | Hermann | Mar 1992 | A |
5296518 | Grasel et al. | Mar 1994 | A |
5552449 | Sollers et al. | Sep 1996 | A |
5591779 | Bleys et al. | Jan 1997 | A |
5961961 | Dobkowski et al. | Oct 1999 | A |
6271277 | Bleys et al. | Aug 2001 | B1 |
6391233 | Otani et al. | May 2002 | B1 |
6638986 | Falke et al. | Oct 2003 | B2 |
6706775 | Hermann et al. | Mar 2004 | B2 |
7427412 | Painter et al. | Sep 2008 | B1 |
7612160 | Nguyen-Kim et al. | Nov 2009 | B2 |
8784854 | Choi et al. | Jul 2014 | B2 |
9532637 | Choi et al. | Jan 2017 | B2 |
20020182245 | Thomson | Dec 2002 | A1 |
20040170670 | Smith et al. | Sep 2004 | A1 |
20050159500 | Dreier et al. | Jul 2005 | A1 |
20060235100 | Kaushiva et al. | Oct 2006 | A1 |
20070189975 | Thomson | Aug 2007 | A1 |
20090047495 | Hubbs | Feb 2009 | A1 |
20110014254 | Choi et al. | Jan 2011 | A1 |
20140023689 | Kim et al. | Jan 2014 | A1 |
20150196468 | Kim et al. | Jul 2015 | A1 |
Number | Date | Country |
---|---|---|
875638 | Aug 1979 | BE |
2356460 | May 1974 | DE |
0528705 | Sep 2000 | EP |
1498363 | Jan 1978 | GB |
08325125 | Dec 1996 | JP |
3015878 | Mar 2000 | JP |
2002-53640 | Feb 2002 | JP |
2003012457 | Jan 2003 | JP |
2004267277 | Sep 2004 | JP |
2005-152186 | Jun 2005 | JP |
2006241150 | Sep 2006 | JP |
2007330771 | Dec 2007 | JP |
2010-6294 | Jan 2010 | JP |
4588357 | Dec 2010 | JP |
0131075 | Nov 1997 | KR |
100498655 | Jul 2005 | KR |
1020090100643 | Sep 2009 | KR |
1020130116044 | Oct 2013 | KR |
1020140038880 | Mar 2014 | KR |
1020150063196 | Jun 2015 | KR |
9947127 | Sep 1999 | WO |
2008112139 | Sep 2008 | WO |
2009116817 | Sep 2009 | WO |
2012128589 | Sep 2012 | WO |
Entry |
---|
“100% Open Cell Flexible Polyurethane Foams”, FXI Reticulated Foams, Product Sheet, FXI, Inc., Retrieved from the Internet Nov. 22, 2016, 1 page, <URL: fxi.com>. |
“BB Cushion Sponge is Melting”, Posted on the Internet Feb. 4, 2015, <URL: http://www.todayhumor.co.kr/board/view.php?table=fashion&no=142195>. |
“Filters for Fishkeeping”, EMW filtertechnik, Product Brochure, Retrieved from the Internet Nov. 22, 2016, pp. 1-4, <URL: www.emw.de>. |
“Nature Republic CC Cushion Pact Sponge Gets Melted!!”, Posted on the Internet Feb. 5, 2015, <URL: http://blog.naver.com/clawsome/220263606984>. |
“Reticulated (Open-Cell) & Non-Reticulated (Closed-Cell) Foam Swabs”, Berkshire, Retrieved from the Internet Nov. 11, 2016, pp. 1-5, <URL: http://www.berkshire.com/shop/cleanroomcleaningswabs/foam.html>. |
“Reticulated Foam” and “Open Cell Polyurethane Foam”, Foam Engineers Limited, Retrieved from the Internet Jul. 8, 2016, pp. 1-2, <URL: http://www.foamengineers.co.uk/foammanufacturingsuppliers/reticulated-foam>. |
“Reticulated Foam-Polyurethane-based foam with open cellular structure”, material sample shop.com, Retrieved from the Internet Jul. 8, 2016, pp. 1-2, <URL: https://www.materialsampleshop.com/products/reticulatedfoampolyurethane-based-foam-with-open-cellular-structure>. |
“Reticulated Open Cell Black Packaging Foam with Polyester Polyurethaner Material”, Changzhou Dayetengfei Sponge Factory, Retrieved from the Internet Jul. 8, 2016, pp. 1-3, <URL: http://www.customizedfoam.com/sale-7566632-reticulatedopen-cellblack-packaging-foam-with-polyesterpolyurethaner-material.html>. |
“Reticulated Polyurethane Foam”, FXI Innovations, Retrieved from the Internet Nov. 11, 2016, pp. 1-3, <URL: http://fxi.com/foamtechnologies/processes/reticulation.php>. |
“Reticulated Polyurethane Foam”, UFP Technologies, Retrieved from the Internet Jul. 8, 2016, pp. 1-3, <URL: http://www.ufpt.com/materials/foam/reticulatedpolyurethane-foam.html>. |
“Reticulated Polyurethane Foam: Quenching vs. Zapping”, UFP Technologies, Retrieved from the Internet May 12, 2016, <URL: http://www.ufpt.com/resource-center/quenching-vs-zappingreticulated-polyurethane/>. |
“Trend of Global Urethane Raw Materials and Products Market”, KIET Overseas Industrial Information, Retrieved from the Internet Nov. 15, 2016, pp. 1-2, <URL: http://www.kiet.go.kr/servlet/isearch?mode=view&dataNo=43619>. |
“Optimization Technology Support for Polyurethane Foam Production through Analysis of Correlations Between CellStructure and Properties”, Ministry of Commerce, Industry and Energy, Sep. 30, 2003, pp. 8, 11 and 12, KR. |
Canadian Office Action for corresponding Canadian Patent Application No. 2,804,298 dated Jan. 18, 2017, citing previously filed reference. |
Canadian Office Action for corresponding Canadian Patent Application No. 2,804,298 dated Jan. 4, 2016, citing U.S. Pat. No. 3,133,309 and previously filed references. |
Canadian Office Action for corresponding Canadian Patent Application No. 2,804,298 dated Sep. 12, 2016. |
Canadian Office Action—Canadia Application No. 2804298 dated May 29, 2014. |
Canadian Office Action—Canadia Application No. 2804298 dated Oct. 28, 2013. |
Canadian Office Action—Canadian Application No. 2804298 dated May 6, 2015, citing U.S. Pat. No. 3,133,309. |
Canadian Protest—Canadia Application No. 2804298 dated Mar. 30, 2015, citing U.S. Pat. No. 3,133,309. |
Chang-Seop Oh, “Recent Prospect of Polyurethanes”, ReSEAT Analysis Report, Sep. 10, 2004, pp. 1-7, KR. |
Chinese Office Action for corresponding Chinese Patent Application No. 201280002267.3 dated Mar. 30, 2016. |
Chinese Office Action—Chinese Application No. 201280002267.3 dated Dec. 3, 2014, citing previously filed references CN101977587 and JP4588357. |
Chinese Office Action—Chinese Application No. 201280002267.3 dated Mar. 18, 2014, citing previously filed references CN101977587 and US20090047495. |
Chinese Office Action—Chinese Application No. 201280002267.3 dated Sep. 8, 2015. |
Chinese Patent Invalidation Request for corresponding Chinese Patent Application No. 201280002267.3. |
European Office Action for corresponding European Patent Application No. 12759918.1 dated Mar. 1, 2016. |
European Office Action—European Application No. 12759918.1 dated Aug. 11, 2015. |
European Office Action—European Application No. 12759918.1 dated Jun. 18, 2015, citing U.S. Pat. No. 3,133,309. |
European Office Action—European Application No. 12759918.1 dated Oct. 12, 2014. |
European Search Report—EP Application No. 12759918.1 dated Jan. 22, 2014 from European Patent Office. |
Extract from pp. 22-23 of Korean Patent Court Ruling (case No. 2016heo8667), 1 page. |
Foaming Plant, Copyrights 2006, pp. 1-7, Retrieved from the Internet Jun. 25, 2018<URL:http://www.foamtecintl.com/index.php?shpage=vpage&vpage=fpprofile&lang=en&plan=FP>. |
George Woods, “Flexible Polyurethane Foams”, Chemistry and Technology, 1982, pp. 94-95, Applied Science Publishers Ltd., Essex, England. |
Indian Office Action—Indian Application No. 10805/CHENP/2012 dated Jul. 14, 2017, citing references listed within. |
INOAC—Reticulated PU Foam, Posted: Nov. 2009, p. 1, Retrieved from the Internet Sep. 2, 2015, <URL: http://www.inostech.com/>. |
International Search Report for International Application No. PCT/KR2012/002141 dated Oct. 31, 2012. |
Japanes Office Action—Japan Application No. 2014-008657 dated Jun. 18, 2015. |
Japanese Office Action for corresponding Japanese Patent Application No. 2014-008657 dated Mar. 9, 2017, citing previously filed reference. |
Japanese Office Action for corresponding Japanese Patent Application No. 2014-008657 dated May 31, 2016, citing previously filed reference. |
Japanese Office Action—Japan Application No. 2014-008657 dated Sep. 11, 2015. |
Jong-Rae Park, “Catalytic Glycolysis of Polyether Urethane Foam Waste”, Master's Thesis, Chonnam National University Graduate School, Department of Chemical Engineering, Aug. 1999, pp. 4-5, KR. |
Korean Office Action with English Translation for Application No. 10-2011-0026466 dated Dec. 16, 2012. |
Korean Office Action with English Translation for Application No. 10-2011-0026466 dated Jun. 6, 2012. |
Malaysian Examination Report—Application No. PI2013000328 dated Apr. 3, 2015, citing previous filed references. |
Notice of Allowance with English Translation for Application No. 10-2011-0026466 dated Apr. 17, 2013. |
Notice of Opposition for EP 12759918.1 from European Patent Office dated Jul. 19, 2018, citing the above references. |
Open Cell Foam, The Foam Factory, Retrieved from the Internet Nov. 11, 2016, pp. 1-2, <URL: http://www.thefoamfactory.com/opencellfoam/filter.html>. |
Polyurethane Foam, p. 1, <URL: http://web.archive.org/web/20090220164156/http://casefoam.com/Polyurethane-foam.htm>. |
Polyurethane Foam, Retrieved from the Internet Nov. 15, 2016, pp. 1-2, <URL: https://web.archive.org/web/20021223120233/http://www.casefoam.com/Polyurethanefoam.htm>. |
Tony Abisaleh et al., “Polyurethane Technology & Applications”, 18 pages. |
Result report of reproduction experiments on Amorepacific's patent (No. 1257628), dated 2017, 21 pages. |
Reticulated foam, Edited on Jun. 3, 2018, pp. 1-3, Retrieved from the Internet Jun. 15, 2018 <URL:https://en.wikipedia.org/wiki/Reticulated_foam>. |
“Reticulated Polyurethane Foam”, UFP Technologies, Retrieved from the Internet Jul. 8, 2016, pp. 1-3. |
Reticulated Foam, Australian Foam Manufacturer, Joyce Foam Products, Retrieved from the Internet Nov. 10, 2016, <URL: http://www.joyce.com.au/foams/reticulatedfoam/>. |
Seong-Mi Park, “Report on Stability Test of Sponge Impregnated with LLBB Cushion Cosmetic Composition”, Cosmax R&I Institute, Apr. 19, 2017, pp. 1-5, Korea. |
Sang-Beom Kim, “About Structure and Properties of Polyurethane Foam”, Letter of Opinion, May 9, 2016, pp. 14. |
Shimin Wu, et al., “Concise Dictionary of Fine Chemicals”, Shenyang: Liaoning Science and Technology, (Jun. 1999), pp. 1-7. |
Singaporean Written Opinion—Application No. 201209361-3 dated Sep. 9, 2013, citing previous filed references. |
Taiwanese Office Action—TW Application No. 101109975 dated Jan. 13, 2014, citing previous filed references. |
Taiwanese Office Action—TW Application No. 101109975 dated Feb. 10, 2014, citing previous filed references. |
UFP Technologies—Reticulated Foam, (Copyright 2011), pp. 1-2, Retrieved from the Internet Sep. 2, 2015, <URL: http://www.ufptcom/>. |
Written Opinion for International Application No. PCT/KR2012/002141 dated Oct. 31, 2012. |
Decision of Intellectual Property Trial and Appeal Board, 6th Department, Trial No. 2018Dang (decision reversing the original decision)76. |
Decision of Intellectual Property Trial and Appeal Board, 7th Department, Trial No. 2018Jeong49. |
Decision of Patent Court, 1st Dvision, Case No. 2016Heo8667 Invalidation of Registration (Patent). |
Decision of Supreme Court, 1st Division, Case No. 2018Hu10596 Invalidation of Registration (Patent). |
Kamicokrolock, “Review, Etude house Cushion Foundation”, web-site contents, Mar. 14, 2015, 3 pages. |
Merquinsa, Polyurethane Types, Web site contents, pp. 1-8. |
Meyer R. Rosen (ed.), Delivery System Handbook for Personal Care and Cosmetic Products, 2005, pp. 513-525. |
Michael Szycher, Szycher's Handbook of Polyurethanes, 1999, p. 7-6. |
Michael Szycher, Szycher's Handbook of Polyurethanes, 1999, pp. C-8, 21, and 24. |
Mihail Ionescu, “Chemistry and Technology of Polyols for Polyurethanes”, 2005, pp. 2-4, 49-50, 263, 538-540, 547, Rapra Technology Limited. |
Polyurethane Technology & Applications, pp. 107-108. |
Polyurethane Technology & Applications, pp. 311-330. |
Polyurethane Technology & Applications, pp. 3-5, 89-90, 123, 125, 169-171, 223-226. |
Seong-Mi Park, Researcher's Statement, COSMAX R&I Institute, Apr. 17, 2017, 1 page. |
T. Thomson, Design and Applications of Hydrophilic Polyurethanes, 2000, pp. 1-9, Preface xi-xiii. |
Test Result Sheet, “Stability Test of LLBB Cushion”, Korea Conformity Laboratories, 2017, pp. 1-5. |
www.ifacemaker.com, a review on ALMAY Nearly Naked Foundation, May 29, 2003. |
Alain Parfondry, “Polyurethane Technology & Applications”, 15 pages, Nov. 2002. |
Declaration of R. Randall Wickett, Petition for Inter Partes Review of U.S. Pat. No. 8,784,854 under U.S.C. §§311-319 and 37 C.F.R. §§42.1-.8, 42.100-,123, Jul. 27, 2018, 90 pages. |
The HLB System, a time-saving guide to emulsifier selection, 22 pages, Mar. 1980. |
Declaration of Robert Y. Lochhead, Ph.D., FRSC, Case IPR2018-01516, U.S. Pat. No. 8,784,854 B2, dated Nov. 30, 2018, 185 pages. |
Petition for Inter Partes Review of U.S. Pat. No. 8,784,854 under U.S.C. §§311-319 and 37 C.F.R. §§42.1-.8, 42.100-.123, dated Aug. 6, 2018, 78 pages. |
Patent Owner's Preliminary Response, Case IPR2018-01516, U.S. Pat. No. 8,784,854 B2, dated Nov. 30, 2018, 70 pages. |
Decision: Denying Institution of Inter Partes Review 35 U.S.C. § 314(a), Case IPR2018-01516, U.S. Pat. No. 8,784,854 B2, Feb. 20, 2019, 29 pages. |
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20190117524 A1 | Apr 2019 | US |
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Parent | 14034650 | Sep 2013 | US |
Child | 16221583 | US |
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Parent | PCT/KR2012/002141 | Mar 2012 | US |
Child | 14034650 | US |