AU536031B2 - Coating composition for forming retroreflective treatments onfabrics - Google Patents

Coating composition for forming retroreflective treatments onfabrics

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Publication number
AU536031B2
AU536031B2 AU65774/80A AU6577480A AU536031B2 AU 536031 B2 AU536031 B2 AU 536031B2 AU 65774/80 A AU65774/80 A AU 65774/80A AU 6577480 A AU6577480 A AU 6577480A AU 536031 B2 AU536031 B2 AU 536031B2
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Australia
Prior art keywords
microspheres
composition
fabric
coating
volume
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
AU65774/80A
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AU6577480A (en
Inventor
Wallace Karl Bingham
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3M Co
Original Assignee
Minnesota Mining and Manufacturing Co
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Filing date
Publication date
Priority claimed from US06/094,696 external-priority patent/US4263345A/en
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Publication of AU6577480A publication Critical patent/AU6577480A/en
Application granted granted Critical
Publication of AU536031B2 publication Critical patent/AU536031B2/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Description

Description
COATING COMPOSITION FOR FORMING RETROREFLECTIVE TREATMENTS ON FABRICS
Technical Field The present invention provides new coating compositions useful for coating fabrics to make them brightly visible under retroreflective viewing conditions without significantly changing their ordinary daylight appearance.
Background Art U.S. Pat. 4,103,060 teaches retroreflective treatments that comprise retroreflective glass microspheres adhered over the surface of a fabric in a low-density, scattered or spaced arrangement. Such treatments are difficult to detect under ordinary daylight viewing conditions; but the coated garments are brightly visible when viewed in the dark under retroreflective viewing conditions (i.e., with the observer located on substantially the same axis as a light beam shined at the fabric). The low daytime visibility of these treatments gives promise of overcoming consumer's resistance to prior retroreflective treatments, which were readily visible during ordinary or casual viewing in daylight.
The specific methods and materials taught in U.S. Pat. 4,103,060 for preparing the described retroreflective treatments have not become commercial. The principal method was to cascade particles onto the fabric particles under conditions which softened a binder material in the particles and adhered them to the fabric. The method did not seem adapted to existing fabric-treating methods; and with some tightly woven fabrics the applied particles protruded above the surface of the fabric and had more daytime visibility than desired. Another method taught in U.S. Pat. 4,103, 060 was to print retroreflective coating compositions onto a fabric in a pattern of spaced areas. Useful retroreflective coating compositions based on hemispherically reflectorized glass microspheres had been taught in Palmquist et al, U.S. Pat. 2,963,378, and further teachings appeared in
Nellessen, U.S. Pats. 3,099,637; 3,228,897; Nellessen et al, U.S. Pat. 3,420,597; Longlet et al, U.S. Pat. 3,535,019 (compositions particularly intended for coating fabrics); Searight, U.S. Pat. 3,835,087; and Hogseth et al, Canadian Pat. 935,254.
The coating of discrete separated areas has not become commercial either. It was difficult to apply sufficient microspheres to provide desired levels of reflectivity without also causing too great daytime conspicuity. Also, the printing operation left a regular pattern that increased the daytime visibility of the treatment.
Disclosure of Invention
The present invention provides new coating compositions that may be coated onto a wide range of fabrics to provide retroreflective treatments that are especially difficult to detect under ordinary daylight viewing conditions. Briefly, a composition of the invention comprises a) a dilute coating vehicle that comprises film-forming binder material and at least 40 volume-percent volatile constituent, and b) transparent microspheres havings a refractive index between about 1.85 and 2 hemispherically coated with specular reflective means and disperserd in the coating vehicle in an amount accounting for no more than about one-third of the volume of the nonvolatile portion of the composition.
Compositions of the invention differ from prior art coating compositions in important ways — including the concentration of microspheres in the coating composition. The prior-art coating compositions were generally int ended to provide coatings having as dense a concentration of microspheres as possible. For that reason, microspheres constituted a large proportion, i.e., 50 volume-percent or more, of the nonvolatile components of the composition. Based on the principles and objectives of these prior-art teachings, a reduction of the concentration of microspheres to the amounts used in the present invention would take away utility. But to the contrary, it has now been found that a reduced concentration of microspheres dispersed in a dilute coating vehicle allows preparation of daytime- inconspicuous, nightime-retroreflective treatments needed to achieve broadly wearable garments. More specifically, it has been found that when a composition as described is coated onto a fabric — as by spreading with a knife blade, coating from a rotogravure cylinder, or spraying — it provides a sparse distribution of microspheres over the surface of the fabric. The binder material in the coating vehicle becomes distributed across the surface of the fabric, and upon drying and/or reaction forms a thin layer holding the microspheres to the fabric. Individual microspheres are partially embedded in the layer and partially protrude above the layer. The microspheres may be randomly oriented, but typically, on the average at least one-third of them are arranged with the hemispherical reflector between the microsphere and the fabric, and with the outwardly facing surface of the microspheres optically exposed. Some useful characteristics noted in the coating include: 1) The microspheres are well distributed across the .surface of the fabric. By choice of the volume-percent of microspheres in the composition, the microspheres can be distributed at densities within the parameters taught in the previously noted Bingham and Bailey, U.S. Pat. 4,103,060, i.e., at a density of no more than about 2000,.and preferably no more than about 500, per square centi meter of the coating.
2) Any .concentrations of microspheres are small, with many of the microspheres isolated or separated from other microspheres of the treatment. The maximum surface dimension of discrete retroreflective areas, i.e., concentrations or clusters of microspheres that are seen as one retroreflective area during retroreflective viewing, is no more than about one millimeter.
3) The microspheres tend to nestle in recesses in the surface of the fabric, i.e., in the valleys or interstices between yarns of the fabric. This nestling minimizes removal of the microspheres during ordinary use and reduces daylight visibility of the microspheres. Coating compositons of the invention are useful on a wide variety of fabrics, including tightly woven fabrics such as nylon used in exterior shells for jackets. and coats.
Overall, a treatment of the invention is difficult to detect in daylight viewing. The microspheres are very small, often on the order of 50 micrometers in diameter or less, and even clusters of microspheres are not easily visible. Individual microspheres isolated from other microspheres are especially hard to detect. (Visual acuity of the human eye is typically regarded as one minute of arc for subjects illuminated under normal lighting conditions of 100-1000 foot-lamberts; at viewing distances of 15 and 30 inches, one minute of arc covers, respectively, 0.0043 inch (110 micrometers) and 0.0087 inch (221 micrometers)).
In contrast to their daytime inconspicuity, garments treated with coating compositions of the invention are brightly retroreflective at night when illuminated by the headlight beam of a vehicle. Under such retroreflective viewing conditions, each properly oriented microsphere sends back a pinpoint of light. In the aggregate, the myriad pinpoint reflections make the fabric bright and visible. Brief Description of the Drawing
The drawing is a schematic representation in section of a fabric 10 that has been retroreflectorized with a composition of the invention. The retroreflective treatment comprises a coating or thin layer 11 of binder material in which hemispherically reflectorized microspheres 12 are partially embedded. The microspheres tend to be deposited in recesses or valleys 13 of the fabric, and may be randomly oriented. Typically at least about one-third of the microspheres are oriented with their hemispherical reflective cap 14 disposed between the microsphere and the fabric and with the outwardly facing surface 15 of the microsphare optically exposed so as to receive light rays.
Detailed Description
Binder materials that are useful for incorporation into coating compositions of the invention are already well known in the fabric-treating industry. Such binder materials have been used for textile printing (as for ornamental purposes), water-proof coatings, flocking binders, etc. These useful binder materials form durable adherent films when coated on a fabric and exposed to an appropriate environment.
Aqueous emulsions of acrylic-based polymers are preferred binder materials, because of the advantages of water as an inexpensive, convenient, and environmentally safe diluent, and because the acrylic polymers provide a durable well-adhered layer that leaves the fabric supple and flexible. A fabric treated with such binder materialscan generally be folded upon itself without fracturing the coated layer of binder material, and the fabric will generally handle and feel approximately the same way after treatment as it did before treatment. These aqueous emulsions of acrylic-based polymers dry upon evaporation of water and coalesce as a continuous film. Typically they also can be subsequently reacted to a more insoluble infusible state as by heating. Such a reacted binder material is not readily soluble in usual dry cleaning solvents. Other useful binder materials for use in the coating vehicle of compositions of the invention are vinylidene chloride-based copolymers, polyesters, and polyurethanes. Although preferred reactive binder materials are one-part compositions which may be activated by application of heat, etc., two-part compositions stored separately until the time of coating can also be used.
To minimize the effect of the layer of applied binder material on the fabric, the layer is preferably very thin. Such thinness can be achieved by making the coating vehicle dilute; generally the vehicle includes at least 40 volume-percent, and preferably at least 70 volume-percent, of a volatile constituent. Such a volatile constituent may be a volatile liquid in which latex particles are dispersed or a solvent or thinner. Although water is a preferred volatile constituent, organic liquids may also be used. As discussed above, the number of microspheres within the composition is kept low, so as to provide the low densities of microspheres on fabric which provide desired daytime inconspicuity. Different degrees of daytime inconspicuity will be accepted for different kinds of garments and fashion schemes, and certain fabrics will achieve good daytime inconspicuity even with higher loadings of microspheres. Where full daytime inconspicuity is not needed, the microspheres may comprise up to about onethird of the volume of the nonvolatile ingredients in the composition; but more typically the microspheres comprise less than about one-fifth of the volume of the nonvolatile ingredients in the composition. The combination of daytime inconspicuity and retroreflectivity that seems preferred today is obtained with loadings of microspheres at levels less than about 15 volume-percent.
Generally sufficient microspheres are included in a composition to provide a reflective treatment that exhibits at least 1 candella, and preferably at least 2.5 or 3 candellas, of reflected light per square meter of a treated surface per lux of light that is incident on the surface.
Since the microspheres constitute only a small percentage of the coating composition, they should be well dispersed within the composition immediately prior to application to a fabric. Such a dispersion can be achieved with mechanical stirring techniques. In addition, thixotropic agents such as carboxylmethyl cellulose and polyacrylates can be added to the composition.
The microspheres included in the composition are visibly transparent, usually glass, and are preferably colorless in most embodiments of the invention. Where a hemispherical reflector is applied directly to the microsphere, as is most common, the index of refraction of the glass will be in a range between 1.85 and 2.0, and preferably will be slightly over 1.9. Microspheres of lower refractive index can be used by spacing the hemispherical reflector from the microsphere, as by precoating a glass microsphere with a material of lower refractive index. And microspheres of high index of refraction can be used in mixture with lower-index microspheres to obtain useful retroreflection when the microspheres are wet. The microspheres are generally less than 200 micrometers in average diameter, and preferably are less than 100 micrometers in average diameter, to minimize their visibility on treated fabric. Procedures for hemispherically reflectorizing microspheres are taught in Palmquist et al, U.S. Pat. 2,963,378. Vapor-coated aluminum is the preferred hemispherical reflective coating, but dielectric coatings such as taught in Bingham, U.S. Pat. 3,700,305 (which is incorporated herein by reference) might also be used. Barrier films, such as aluminum phosphate or aluminum oxide films, may be applied over a metal hemispherical coating in the manner taught in Longlet et al, U.S. Pat. 3,535,019, to increase the shelf-stability of compositions of the invention. Alternatively or in addition, additives such as 6-acetoxy-2,4-dimethyl-m-dioxane or trans-1,2-bis (n- propylsulfonyl) ethylene may be included in the coating vehicle to increase shelf-stability; these additives are understood to inhibit microbial growth.
A variety of other additives may be included in the composition to achieve special results. For example, anti-foaming agents may be included in the coating vehicle to minimize foaming of the vehicle as it is being formulated or when it is applied to a fabric. Other additives which may be included in the composition are organofunctional silanes and transparent pigments and dyes, which are included as adhesion aids or coupling agents and as camouflaging or coloring compounds.
The preferred technique for applying a coating composition of the invention to a fabric is to spread the composition across the fabric with dam or barrier means such as a knife blade. The knife blade may be lightly pressed against the surface of the fabric or may be elevated above the fabric a slight amount and moved across the fabric. The coating composition moves ahead of the knife blade, with only a thin layer of coating vehicle being applied over the surface of the fabric, and with most of the microspheres tending to be deposited in recesses in the fabric. Because of the low concentration of nonvolatile binder material in the coating vehicle, the vehicle is reduced upon drying to a very thin film. Some penetration of the binder material into the fabric occurs as represente by penetration of the binder material 11 in the attached drawing. Instead of spreading composition across a fabric with a knife blade, the composition may be applied by other techniques such as rotogravure rolls, sprays or spray and knife-blade combinations, or screen printing. The invention will be further illustrated with the following examples. A coating composition was prepared from the following ingredients.
Parts by Weight
Aqueous emulsion comprising 54 weight-percent water and 46 weight-percent of a copolymer of ethyl acrylate and methylol acrylamide (Rhoplex HA-8 from Rohm & Haas Company) 26.6
Aqueous emulsion containing 80 weight-percent water and 20 weight-percent copolymer of ethyl methacrylate and acrylic acid used as thickener
(Acrysol ASE95 from Rohm & Haas Company) 0.7
Anti-foaming agent (Nopco DF160L from Diamond Shamrock Company; diluted with 50 percent water) 0.9
Ammonium nitrate catalyst enhancing cure of acrylic-based polymer (diluted with 75 percent water) 0.4
Silane coupling agent (Dow Corning Z6040) 0.9
Nitrogenous thermosetting resin catalyst agent (Arotex M-3 from American Cyanamid Company) 0.9
Hemispherically aluminized glass microspheres of approximately 1.92 refractive index averaging 45 micrometers in diameter and ranging between
21 and 63 micrometers in diameter 6 . 4
Water 53.2
The described ingredients were mixed together and adjusted to a pH of 8 with ammonium hydroxide to prepare a coating composition having a viscosity of about 1700 centipoises. The microspheres constituted 1.84 volume-percent of the total coating composition and 11.58 percent of the nonvolatile components of the composition.
The composition was coated onto a tightly-woven nylon oxford fabric using a knife blade riding directly against the fabric. The composition was dried by forced air heated to 150°F (66°C) and subsequently was heated for 10 minutes at 305°F (150°C) to cure the binder material. The fabric was found to be coated with a continuous layer of binder material with microspheres distributed over the surface of the fabric at a density of about 1450 microspheres per square centimeter. Almost all the microsphere rested in recesses in the surface of the fabric. When the fabric was viewed in ordinary daylight the microspheres could not be detected except upon very close inspection with the eye. At nighttime the fabric was brightly retroreflective, providing 2.5 candella of reflected light per square meter of treated surface per lux of incident light.

Claims (5)

1. Coating composition useful for retroreflectorizing fabrics comprising a) a coating vehicle that includes film-forming binder material and a volatile constituent, and b) transparent microspheres having a refractive index between about 1.85 and 2 hemispherically coated with specular reflective means and dispersed in the coating vehicle; characterized in that the volatile constituent comprises at least 40 volume-percent of the coating vehicle, and the transparent microspheres account for about one-third or less of the volume of the nonvolatile portion of the composition.
2. Composition of claim 1 in which the binder material comprises an aqueous emulsion of acrylic-based polymer.
3. Composition of claim 1 or 2 in which the microspheres account for about one-fifth or less of the volume of the nonvolatile portion of the composition.
4. Composition of claim 1, 2 or 3 in which the vehicle includes at least 70 volume-percent of a volatile constituent.
5. A method of forming a retroreflective treatment on fabric comprising spreading a composition of any of claims 1-4 across the fabric with barrier means.
AU65774/80A 1979-11-16 1980-10-14 Coating composition for forming retroreflective treatments onfabrics Ceased AU536031B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US094696 1979-11-16
US06/094,696 US4263345A (en) 1979-11-16 1979-11-16 Coating composition for forming retroreflective treatments on fabrics
PCT/US1980/001377 WO1981001471A1 (en) 1979-11-16 1980-10-14 Coating composition for forming retroreflective treatments on fabrics

Publications (2)

Publication Number Publication Date
AU6577480A AU6577480A (en) 1981-06-03
AU536031B2 true AU536031B2 (en) 1984-04-12

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AU6577481A Pending AU6577481A (en) 1979-11-16 1980-10-14 Coating composition for forming retroreflective treatments onfabrics

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU574410B2 (en) * 1983-12-07 1988-07-07 Filtrol Corp. Coated scintillator crystal

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU574410B2 (en) * 1983-12-07 1988-07-07 Filtrol Corp. Coated scintillator crystal

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Publication number Publication date
AU6577481A (en) 1981-06-03

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