The present application relates to an article of apparel and, in particular, a garment including a textile adapted to regulate thermal conditions of the wearer and methods of forming the textile.
The heat retention of a planar textile structure generally increases with increasing thickness. As thickness of the textile increases, however, resistance to the passage of moisture also increases. This results in apparel that, while warming, can cause the skin to be covered with uncomfortable perspiration. Accordingly, it would be desirable to form apparel from a textile that, while light, is capable of heat retention and transfers perspiration from the wearer.
The present invention is directed toward a process of forming a textile and apparel formed utilizing the textile. The textile includes a base layer and a spacer layer defined by a plurality of spacer elements extending distally from the base layer. In an embodiment, the spacer elements are oriented in a grid pattern, being spaced apart to define gaps for air circulation. Selected spacer elements are mechanically compressed and secured in the compressed state utilizing an adhesive composition. The adhesive composition may further include heat insulating or heat reflective particles. The resulting textile may be utilized to form articles of apparel, including garments such as shirts, pants, coats, footwear, and underwear.
Like numerals refer to like components throughout the figures.
With reference to
The spacer elements 115 are arranged in a predetermined pattern along the interior surface of the first textile portion 105 such that channels or gaps between adjacent elements. In an embodiment, the spacer elements 115 are disposed in an array. By way of example, the spacer elements 115 form a matrix, i.e., a rectangular array of elements ordered in columns 120 and rows 125 (
Referring to
Referring to
The textile 10—the first textile portion 105 and the second textile portion 110—may be formed of the same or similar yarn. By way of example, the textile portions 105, 110 may be formed of hydrophobic yarn such as polyester or polypropylene. In another embodiment, the textile portions 105, 110 may be formed of hydrophilic yarn such as cotton or wool. In still other embodiments, the textile portions 105, 110 may be formed of a combination of hydrophobic and hydrophilic yarns. In a preferred embodiment, the textile 10 (the first 105 and second 110 textile portions) is formed of hydrophobic yarn (e.g., polyester) provided with hydrophilic properties, e.g., via chemical treatment (such as a conventional wicking finish).
In other embodiments, the first textile portion 105 and the second textile portion 110 are formed of yarns having different properties. By way of example, the second textile portion 110 may be formed of untreated hydrophobic yarn and the first textile portion 105 may be formed of hydrophobic yarn treated such that it possesses hydrophilic properties 110. By way of further example, the second textile portion 110 may be formed of hydrophobic yarns and the first textile portion 105 may be formed of hydrophilic yarns. By way of still further example, the yarns of the first portion 105 and/or the second portion 110 may be treated with a durable water repellant (DWR) composition. Additionally, the denier of the yarns forming the first 105 and second 110 portions may differ (e.g., the denier of the first portion yarns may be greater than the denier of the second portion yarns).
With the above configuration, a textile 10 including channels 130, 135 or pockets 140 is formed. The spacer elements 115 and the channels 130, 135 or pockets 140 cooperate to control movement of fluid within and through the textile 10. Regarding liquid, the structure drives liquid from the second textile portion 110 to the first textile portion 105. Specifically, when fluid contacts the surface of a spacer element 115, it is drawn/moved along the length/height of the spacer element and into the first textile portion 105, where it diffuses/spreads. Additionally, when liquid falls directly into a channel 130, 135 or pocket 140, the liquid immediately contacts the first textile portion 105 where it diffuses/spreads.
Alternatively, when the spacer elements 115 are non-wicking and/or hydrophobic, the liquid may contact the spacer elements 115, rolling off the spacer element into the channel 130, 135 or pocket 140. To this end, as mentioned above, the spacer elements 115 may be configured with a tapered 210 or rounded 215 edge, assisting in fluid roll off (
With these configurations, liquid from the user (i.e., sweat) is immediately directed from the spacer element 115 and into a channel 130, 135 or pocket 140. In other words, liquid is directed from the second textile portion 110 to the first textile portion 105, where the liquid is held away from the skin of the wearer. This improves wearer comfort.
It should be noted that the yarn may be selected to impart desired fluid absorption characteristics to the textile. That is, the first textile portion 105 may possess a first sorptivity (capillary action) value and the second textile portion 110 may possess a second sorptivity (capillary action) value. In an embodiment, the first sorptivity value is greater than the second sorptivity value (e.g., when the first portion is hydrophilic and the second portion is hydrophobic). In another embodiment, the first sorptivity value is less than or equal to the second sorptivity value. In a preferred embodiment, the first textile portion 105 generates greater capillary action (and thus possesses higher fluid sorptivity) than the second textile portion 110.
It should also be understood that while the textile portions 105, 110 may be generally hydrophobic or hydrophilic, the relative degree of the relevant property may differ. For example, while the first textile portion 105 and the second textile portion 110 may be considered hydrophobic, the second textile portion 110 may be less hydrophobic than the first textile portion 105 (and vice versa), i.e., the second textile portion experiences a greater moisture pick-up under a standard atmosphere (moisture pick up being measured by the mass of absorbed and adsorbed water that is held by a material). Similarly, while both textile portions 105, 110 may be considered generally hydrophilic, the second textile portion 110 may be less hydrophilic than the first textile portion 105 (and vice versa). Alternatively, the portions 105, 110 may possess identical wicking properties.
Along with liquid flow, the textile structure 10 further enables movement of air along and through the textile 10. While both the first textile portion 105 and the second textile portion 110 are air permeable, the air permeability of the textile 10 along a channel 130, 135 or pocket 140 is greater than the air permeability of the textile along a spacer element 115. Accordingly, the channels 130, 135 or pockets 140 capture air and direct it out through the textile 10 (via the first textile portion 105), enhancing air flow during physical activity, thereby creating a heat dissipating or cooling effect. In a preferred embodiment, the first textile portion 105 possesses higher vapor permeability (breathability) than the second textile portion 110 (in its unprinted state).
The textile 10 may be formed utilizing any process suitable for its described purpose. In an embodiment, the textile 10 is knitted to form a unitary structure. By way of example, the textile is formed via warp knitting. By way of further example, the textile 10 is a double knit jacquard formed via a process that simultaneously forms both textile portions 105, 110. While forming the second textile portion 110, knitting is selectively started and stopped at predetermined positions to form spacer elements 115. Stated another way, the channels 130, 135 or pockets 140 are formed wherever the knitting operation is suspended (creating regions that are substantially free of pile) and spacer elements 115 are formed wherever the knitting operation is resumed (creating regions including pile).
In other embodiments, the textile 10 possesses loop pile construction. By way of example, the textile 10 may be formed as described U.S. Pat. No. 5,065,600 or 5,547,733, the disclosure of each patent is incorporated herein by reference in its entirety. In still other embodiments, the first 105 and second 110 textile portions are independent layers secured together, e.g., via adhesive, stitching, etc. Accordingly, the textile 10 may possess a unitary construction, or may be formed of multiple, distinct layers.
In order to control the properties of the article of apparel, the textile 10 may be processed to selectively seal areas of the fabric and compress the fibers, filaments or yarns forming the textile. In an embodiment, one or both textile portions 105, 110 may be compressed and sealed to minimize its breathability and/or fluid abortion properties. Specifically, the filaments, fibers, or yarns along the surface of a textile portion 105, 110 may compressed by an applicator and secured in its compressed state utilizing an adhesive or sealant composition.
In an embodiment, the textile 10 may be further processed to selectively compress and/or seal one or more of the spacer elements 115, as well as to selectively seal all or part of the channels 130, 135 or pockets 140. Specifically, one or more spacer elements 115 is fully or partially compressed by an applicator and secured in its compressed state utilizing an adhesive or sealant composition. By way of example, the textile 10 may be processed by a rotogravure apparatus configured to simultaneously compress a selected spacer element 115 and apply an adhesive or sealant composition to the compressed spacer element. Referring to
In another embodiment, the rotogravure is a reverse kiss gravure coater. Referring to
In an embodiment, the speed of the roller may be approximately 30 revolutions per minute, and the applied wet coating possesses a thickness of no more than 30 μm.
The adhesive composition 420 may be any adhesive suitable for its described purpose. For example, the adhesive includes a polymeric binder such as polyurethane. Polyurethane, while flexible, is effective to fill the voids of the textile (i.e., the air passages present in each the first textile portion 105 and the second textile portion 110), reducing or preventing air from passing through at its point of application.
The adhesive composition 420 may further include insulating, heat-conducting, or heat-reflecting material dispersed in the binder. By way of example, the adhesive composition 420 may contain inorganic materials such as ceramics (technical ceramics and refractory materials), as well as metals. By way of specific example, the adhesive composition may include silica (SiO2), silicon nitride (SiN), zeolite, zirconium dioxide (ZrO2), calcium silicate, calcium carbonate, aluminum nitride (AlN), alumina (Al2O3), silicon carbide (SiC), and magnesium oxide (MgO), copper, aluminum, etc. In a preferred embodiment, the coating includes silica capable of absorbing thermal energy such as body heat.
In an embodiment, the adhesive composition may possess a viscosity of no more than 1000 mPa·s.
The adhesive composition 420 may be applied in any pattern suitable for its described purpose. In an embodiment, the adhesive composition 420 is applied in an interrupted or discontinuous pattern. Preferably, the discontinuous layer is configured such that the adhesive composition covers no more than 50% the surface area of the textile front face (the user facing face). In an embodiment, the adhesive composition 420 is applied as a vector pattern. Referring to
The pattern 500 may further include a plurality of linear members 505A-505n+1 ordered to form a superstructure 515 such as a polygon and, in particular, a hexagon. As seen in
Referring to
With these arrangements, the linear members 505A-505n+1 can span portions of the wearer, improving the capture and/or distribution of thermal energy (e.g., body heat) generated by the wearer. That is, the linear elements enable the efficient absorption and dispersion of heat over a wider surface area than, e.g., dots or circles. That is, if the first segment 510A of a linear member is positioned over an area of the body generating heat, while the third segment 510B is not, the first segment will initially absorb heat. The absorbed heat will then travel (be conducted) between segments 510A-510n+1. This is in contrast with individual circles or squares, which, being spaced from each other, do not dispersing it along the surface of the wearer.
Formation of the textile 10 with selectively compressed spacer elements is explained with reference to
Accordingly, as shown in
Once transferred, the adhesive composition 420 may completely cover a spacer element 715 (securing the entire spacer element in its compressed configuration) or may partially cover a spacer element 115 (securing a portion of the spacer element in the compressed configuration). Accordingly, the resulting textile 10 includes a plurality of expanded spacer elements 115 extending distally from the first textile portion 105 at a first height and a plurality of compressed spacer elements 715 extending from the first textile portion 105 at a second height, with the second height being less than the first height. Depending on the pressure applied, the distal end of each compressed spacer element 715 may be substantially or completely flush with the textile surface (i.e., with the surface of the first textile portion 105), or may be slightly recessed into the textile surface. In compressed areas not including a spacer element 115, the surface including the compressed fibers, filaments, or yarns may be recessed or substantially flush with the surrounding non-compressed areas, depending on the pressure applied.
The resulting textile 10 (and the article of apparel made therefrom) possesses improved thermoregulatory control compared to a textile lacking the adhesive composition. That is, the textile 10 possesses improved heat retention and distribution capabilities without increasing the overall weight of the textile/article of apparel (or increasing the weight by only a nominal amount). In the sealed areas, transmission of fluid (liquid/air) through the textile 10 is delayed or prevented. Without being bound to a particular theory, it is believed that the binder (e.g., polyurethane) of the adhesive composition 420 seals the textile 10 by covering the pores or openings existing within the fabric, decreasing airflow and liquid flow therethrough. Decreasing the air permeability of the textile (and thus of the article of apparel) increases its insulating properties of the textile. The heat of the wearer, moreover, is retained in the air pockets naturally existing between the wearer and the textile 10 (or between the textile and another fabric layer).
Wearer comfort, however, is maintained. The adhesive composition 420, being applied as a discontinuous layer, maintains the breathability of the textile. In addition, any liquid contacting a sealed area may simply roll of the sealed area to an unsealed area, being moved away from the user.
In addition, the adhesive composition 420 may further include insulation or other heat retaining material, further increasing the insulation properties of the composition, and thus the textile 10 (compared with the textile printed with the adhesive composition lacking insulation material). That is, if the adhesive composition 420 further includes an insulating material, the composition is effective to decrease thermal conductivity through the textile, increasing its absorption of heat. For example, when silica is present in the adhesive composition 420, the silica, having a specific heat capacity value that is greater than that of, e.g., the textile 10 and/or the binder, is capable of absorbing heat from the wearer. Even when the heat energy is removed, the heat retaining material may then release the stored energy, warming the microclimate around the wearer.
In still further embodiments, the heat retaining material may be selected to emit or radiate selected wavelengths back to wearer (e.g., IR waves), when the heat source is removed.
Examples of heat retaining materials include ceramics such as AlO2, ZnO, SnO2, TiO2, SiO2, SiC and ZrC. The heat retaining material may be present in an amount of less than 50 wt % and, in particular, less than 25 wt % (e.g., 2-10 wt %).
If the adhesive composition 420 includes a heat conductive material, the heat of the wearer will be absorbed and will be evenly dispersed along the composition, increasing the overall feeling of warmth, with the heat being transferred from a warmer part of the body to a cooler part.
Finally, if the adhesive composition 420 further includes a heat-reflective material, the composition is effective to reflect the heat of the wearer back towards the wearer, increasing the feeling of warmth.
Regardless of the type of adhesive composition used, the overall fluid control characteristics remain intact since a substantial portion of the channels 130, 135, pockets 140, and/or spacer elements 115 remain exposed (unsealed/unprinted). That is, while overall air permeability (breathability) is reduced, the article of apparel still retains a substantial level of breathability, increasing user comfort. Thus, the invention increases user warmth, adds minimum weight to the textile 10, and retains the base properties of the textile such as breathability.
In this manner, a garment can be provided that, while capable of moving sweat away from the wearer to provide the wearer with a feeling of dryness, also provides a warming effect while worn.
In addition, since the adhesive composition or sealing agent 420 is applied in a discontinuous pattern along the inner fabric surface, the resulting garment includes areas possessing different air permeability and/or heat retention values. Specifically, the area of fabric including the sealing agent possesses a first air permeability value, while the area of fabric not including the sealing agent possesses a second air permeability value. The second air permeability value is higher than the first air permeability value. Additionally, area of fabric including the sealing agent with a heat retaining or insulating material possesses a first heat retention value, while the area of fabric not including the sealing agent with the heat retention material possesses a second heat retention value, with the second heat retention value being lower than the first heat retention value.
When the discontinuous pattern of
The textile 10 formed according to the principles of the present invention may be used in a number of different products. For example, the textile 10 may be incorporated into a shirt 800 (
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof. In at least one embodiment, the ceramic print covers about 25% to about 80% of the interior surface area of the article of apparel (e.g., about 35%-45%).
Thus, it is intended that the present invention covers the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents. It is to be understood that terms such as “top,” “bottom,” “front,” “rear,” “side,” “height,” “length,” “width,” “upper,” “lower,” “interior,” “exterior,” “medial,” “lateral,” and the like as may be used herein, merely describe points of reference and do not limit the present invention to any particular orientation or configuration.
Number | Name | Date | Kind |
---|---|---|---|
2695895 | Barnard et al. | Nov 1954 | A |
3422512 | Law | Jan 1969 | A |
3849802 | Govaars | Nov 1974 | A |
4211261 | Mehta et al. | Jul 1980 | A |
4316931 | Tischer et al. | Feb 1982 | A |
4420521 | Carr | Dec 1983 | A |
4569874 | Kuznetz | Feb 1986 | A |
4622253 | Levy | Nov 1986 | A |
4637947 | Maekawa et al. | Jan 1987 | A |
4856294 | Scaringe et al. | Aug 1989 | A |
5072455 | St. Ours | Dec 1991 | A |
5073222 | Fry | Dec 1991 | A |
5098795 | Webb et al. | Apr 1992 | A |
5265278 | Watanabe | Nov 1993 | A |
5411791 | Forry et al. | May 1995 | A |
5792714 | Schindler et al. | Aug 1998 | A |
6007245 | Looy | Dec 1999 | A |
6089194 | LaBelle | Jul 2000 | A |
6219852 | Bain et al. | Apr 2001 | B1 |
6284380 | Martin | Sep 2001 | B1 |
6321386 | Monica | Nov 2001 | B1 |
6332221 | Gracey | Dec 2001 | B1 |
6415453 | Anderson et al. | Jul 2002 | B1 |
6599850 | Heifetz | Jul 2003 | B1 |
6824819 | Vogt et al. | Nov 2004 | B2 |
6931665 | Feduzi | Aug 2005 | B2 |
7043761 | Epling | May 2006 | B2 |
7217456 | Rock et al. | May 2007 | B1 |
7428772 | Rock | Sep 2008 | B2 |
7743476 | Rock et al. | Jun 2010 | B2 |
7977261 | Szczesuil | Jul 2011 | B2 |
8028386 | Rock et al. | Oct 2011 | B2 |
D655921 | Snyder | Mar 2012 | S |
D657093 | Snyder | Apr 2012 | S |
D666837 | Elser | Sep 2012 | S |
8424119 | Blackford | Apr 2013 | B2 |
8453270 | Blackford | Jun 2013 | B2 |
8479322 | Blackford et al. | Jul 2013 | B2 |
8510871 | Blackford et al. | Aug 2013 | B2 |
20020137417 | Tebbe | Sep 2002 | A1 |
20020189608 | Raudenbush | Dec 2002 | A1 |
20050009429 | Park | Jan 2005 | A1 |
20050053759 | Rock | Mar 2005 | A1 |
20060135019 | Russell et al. | Jun 2006 | A1 |
20070022510 | Chapuis et al. | Feb 2007 | A1 |
20080155729 | Schwarz | Jul 2008 | A1 |
20080189824 | Rock | Aug 2008 | A1 |
20090061131 | Monfalcone et al. | Mar 2009 | A1 |
20090298370 | Rock | Dec 2009 | A1 |
20100058509 | Lambertz | Mar 2010 | A1 |
20100269242 | Stubiger | Oct 2010 | A1 |
20100282433 | Blackford | Nov 2010 | A1 |
20110041230 | Huang et al. | Feb 2011 | A1 |
20110083246 | Vitarana | Apr 2011 | A1 |
20120015155 | Blackford | Jan 2012 | A1 |
20130014311 | Chapuis | Jan 2013 | A1 |
20130160193 | Cremin | Jun 2013 | A1 |
20130209735 | Kim | Aug 2013 | A1 |
Number | Date | Country |
---|---|---|
1094928 | Nov 1994 | CN |
2484763 | Apr 2002 | CN |
101405452 | Apr 2009 | CN |
201509611 | Jun 2010 | CN |
247637 | Jul 1987 | DE |
1816254 | Aug 2007 | EP |
1816254 | Aug 2007 | EP |
2205533 | Dec 1988 | GB |
2350073 | Nov 2000 | GB |
2389073 | Dec 2003 | GB |
01188336 | Jul 1989 | JP |
01207403 | Aug 1989 | JP |
H01207403 | Aug 1989 | JP |
02182968 | Jul 1990 | JP |
03033251 | Feb 1991 | JP |
03051301 | Mar 1991 | JP |
031317284 | Jun 1991 | JP |
03167301 | Jul 1991 | JP |
05186728 | Jul 1993 | JP |
H1150378 | Feb 1999 | JP |
2000129566 | May 2000 | JP |
2000129567 | May 2000 | JP |
2001337601 | Dec 2001 | JP |
2002088647 | Mar 2002 | JP |
2002166505 | Jun 2002 | JP |
2002371465 | Dec 2002 | JP |
2003236971 | Aug 2003 | JP |
2003239111 | Aug 2003 | JP |
3096192 | Sep 2003 | JP |
2006348414 | Dec 2006 | JP |
2010043388 | Feb 2010 | JP |
20030019662 | Mar 2003 | KR |
571009 | Jan 2004 | TW |
200949043 | Dec 2009 | TW |
199707899 | Mar 1997 | WO |
2002032692 | Apr 2002 | WO |
2002103108 | Dec 2002 | WO |
2005049745 | Jun 2005 | WO |
2011114025 | Sep 2011 | WO |
Entry |
---|
Subramanian, Muralisrinivasan Natamai. (2016). Plastics Waste Management—Processing and Disposal—2.1.1.2 Polypropylene. Smithers Rapra Technology. Online version available at:http://app.knovel.com/hotlink/pdf/id:kt01129JVG/plastics-waste-management/polypropylene. |
“Raising.” Complete Textile Glossary. New York, NY: Celanese Acetate, 2001. N. pag. Print. |
Gangolli, S. et al., The Dictionary of Substances and their Effects, 2005, Third Electronic Edition, Royal Society of Chemistry Retrieved from www.knovel.com. |
Koo, Kang et al., The application of PCMMcs and SiC by commercially direct dual-complex coating on textile polymer, Applied Surf ace Science, 2009, 8313-8318, Elsevier B.V. |
Number | Date | Country | |
---|---|---|---|
20150223533 A1 | Aug 2015 | US |
Number | Date | Country | |
---|---|---|---|
61932480 | Jan 2014 | US |