CA1148803A - Polyester textile material having improved opacity - Google Patents
Polyester textile material having improved opacityInfo
- Publication number
- CA1148803A CA1148803A CA000352026A CA352026A CA1148803A CA 1148803 A CA1148803 A CA 1148803A CA 000352026 A CA000352026 A CA 000352026A CA 352026 A CA352026 A CA 352026A CA 1148803 A CA1148803 A CA 1148803A
- Authority
- CA
- Canada
- Prior art keywords
- textile material
- titanium dioxide
- polyester fiber
- dispersion
- textile
- 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.)
- Expired
Links
- 239000004753 textile Substances 0.000 title claims abstract description 157
- 239000000463 material Substances 0.000 title claims abstract description 151
- 229920000728 polyester Polymers 0.000 title claims abstract description 75
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 200
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 95
- 239000006185 dispersion Substances 0.000 claims abstract description 79
- 239000000835 fiber Substances 0.000 claims abstract description 71
- 239000002245 particle Substances 0.000 claims abstract description 70
- 238000000034 method Methods 0.000 claims abstract description 58
- 239000004744 fabric Substances 0.000 claims abstract description 56
- 239000000049 pigment Substances 0.000 claims abstract description 51
- 230000008569 process Effects 0.000 claims abstract description 38
- 239000000758 substrate Substances 0.000 claims abstract description 28
- 238000009998 heat setting Methods 0.000 claims abstract description 9
- 239000002759 woven fabric Substances 0.000 claims abstract description 7
- 239000011230 binding agent Substances 0.000 claims description 33
- 239000002253 acid Substances 0.000 claims description 30
- 238000005406 washing Methods 0.000 claims description 22
- 239000000853 adhesive Substances 0.000 claims description 15
- 230000001070 adhesive effect Effects 0.000 claims description 15
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims description 12
- 238000013019 agitation Methods 0.000 claims description 12
- 238000005054 agglomeration Methods 0.000 claims description 9
- 230000002776 aggregation Effects 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 229930188620 butyrolactone Natural products 0.000 claims description 6
- 239000011164 primary particle Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims 2
- 238000004900 laundering Methods 0.000 abstract description 12
- 238000005108 dry cleaning Methods 0.000 abstract description 11
- 229910044991 metal oxide Inorganic materials 0.000 abstract description 3
- 150000004706 metal oxides Chemical class 0.000 abstract description 3
- 230000014759 maintenance of location Effects 0.000 abstract description 2
- 230000000717 retained effect Effects 0.000 abstract description 2
- 239000002689 soil Substances 0.000 description 16
- 239000000523 sample Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 238000010410 dusting Methods 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 230000002411 adverse Effects 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- -1 e.g. Chemical compound 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000908 ammonium hydroxide Substances 0.000 description 3
- 239000013068 control sample Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000001000 micrograph Methods 0.000 description 3
- 150000003608 titanium Chemical class 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000000635 electron micrograph Methods 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000020477 pH reduction Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 230000002087 whitening effect Effects 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- BCLCSSKWUJDWOK-UHFFFAOYSA-L N.[O-2].[OH-].[OH-].[Ti+4] Chemical compound N.[O-2].[OH-].[OH-].[Ti+4] BCLCSSKWUJDWOK-UHFFFAOYSA-L 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 208000032400 Retinal pigmentation Diseases 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- MJWPFSQVORELDX-UHFFFAOYSA-K aluminium formate Chemical compound [Al+3].[O-]C=O.[O-]C=O.[O-]C=O MJWPFSQVORELDX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- BTVWZWFKMIUSGS-UHFFFAOYSA-N dimethylethyleneglycol Natural products CC(C)(O)CO BTVWZWFKMIUSGS-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000009828 non-uniform distribution Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000004876 x-ray fluorescence Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/46—Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Artificial Filaments (AREA)
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
POLYESTER TEXTILE MATERIAL
HAVING IMPROVED OPACITY
Abstract of the Disclosure A polyester fiber textile material made by the application of titanium dioxide pigment thereto is provided. According to the process by which the textile material is made, the titanium dioxide pigment having a particle size of at least about 0.18 micron is exhausted from a dispersion of same onto the textile material at a pH below approximately 7.5. Subsequent heat set-ting of the polyester textile material improves retention of the titanium dioxide pigment.
It has long been known that textile materials, that is spun yarns, exturded filaments, woven fabrics, knitted fabrics, non-woven materials and the like can be rendered more opaque by the addition of various metal oxides, such as titanium dioxide thereto.
By adding opacity to a sheer textile material, the covering power of the material is greatly improved, without the extra weight and cost that would be present for a heavier, tightly formed substrate.
Likewise, in so adding opacity to the textile material it is quite desirable, if not imperative, to avoid changing the handle characteristics to a point where the material becomes unsuited for garment use, for example, and the improved opacity charac-teristic should be retained after repeated launderings or dry cleanings.
HAVING IMPROVED OPACITY
Abstract of the Disclosure A polyester fiber textile material made by the application of titanium dioxide pigment thereto is provided. According to the process by which the textile material is made, the titanium dioxide pigment having a particle size of at least about 0.18 micron is exhausted from a dispersion of same onto the textile material at a pH below approximately 7.5. Subsequent heat set-ting of the polyester textile material improves retention of the titanium dioxide pigment.
It has long been known that textile materials, that is spun yarns, exturded filaments, woven fabrics, knitted fabrics, non-woven materials and the like can be rendered more opaque by the addition of various metal oxides, such as titanium dioxide thereto.
By adding opacity to a sheer textile material, the covering power of the material is greatly improved, without the extra weight and cost that would be present for a heavier, tightly formed substrate.
Likewise, in so adding opacity to the textile material it is quite desirable, if not imperative, to avoid changing the handle characteristics to a point where the material becomes unsuited for garment use, for example, and the improved opacity charac-teristic should be retained after repeated launderings or dry cleanings.
Description
Titanium dioxide is a suitable material for adding opacity to a textile material. Titanium dioxide addition to a synthetic polymeric filament has often been made by adding same to the polymer melt prior to extrusion of the filaments. Such tech-niques result in dispersion of the titanium dioxide throughoutthe filament cross section. Textile fabrics, spun yarns, non-woven webs, extruded filaments and the like, have been treated after formation wherein the titanium dioxide has been applied to the surface textile materials from pad baths, by spraying, by dipping and the like for various effects, including opacity. In particular, in those instances where the titanium dioxide has heretofore been utilized to add whiteness or opacity to the tex-tile material, an adhesive binder has been included as the primary means for securing same to the textile material for durability purposes both as to "dusting", i.e., removal of the pigment due to surface distortion, and repeated laundering and dry cleaning operations. Generally, however, when a sufficient amount of titanium dioxide is added to appreciably improve opacity of the substrate, the amount of binder previously required has produced a quite stiff substrate. In padding operations, the titanium dioxide also migrates during drying, presenting non-uniform dis-tribution of pigment on the surface of the substrate.
Adhesive binders, and titanium dioxide, either in the form of a titanium salt or a pigment, have heretofore been present in dispersions, solutions or emulsions along with other ingredients and brought into contact with the textile material for normal application thereto. The textile material was thereafter further processed to promote adherence of the various ingredients thereto.
.~ ~
It has further been known to utilize titanium salts in dispersions that are applied to textile materials, such as cellulose acetate, rayon and the like to deluster same. Appli-cation of the metal oxides to deluster a cellulosic substrate has - 5 conventionally utilized a metal salt in the dispersion with the salt thereafter being acid treated to release the metal ions which become affixed to the substrate under acidic conditions. In fact, such processes have historically been operated totally under acid conditions. Other techniques have likewise been utilized for applying titanium dioxide onto textile materials. Exhaustion techniques have been practiced, where the particle size of the titanium dioxide was 0.1 micron or smaller. In such processes, the titanium dioxide is of such particle size as to be colorless and is applied to resist soiling of the textile material without any whitening effect. In other wordsl opacity is not improved.
While all of the above techniques have in fact been pre-viously utilized to apply titanium dioxide and other metal oxides onto textile substrates, no one or combination of same has approached the problem of the present inventi~on, i.e., providing an improved polyester fiber-containing textile material which has been rendered more opaque to the passage of light wherein the material added to improve the opacity is bound to the substrate without the necessity of an adhesive binder as the primary means for bonding the particles to the surface of the textile material, and yet is quite durable to repeated laundering and dry cleaning operations, and compatible with other textile ~inishing opera-tions. Very importantly, relatively large amounts of pigment may be added to the textile substrate without a resultant harsh handle.
It is an object of the present invention to provide a polyester fiber-containing textile material having improved opa-city and to provide a process for preparing same.
-Another object of the present invention is to provide improved polyester fiber-containing textile materials which are more opaque to the transmission of light and which have good handle characteristics and to provide a process for preparing same.
Still another object of the present invention is to pro-vide a process for the adhesion of titanium dioxide to a poly-ester textile material from a bath in the absence of a binder asthe primary means of adhesion and to provide products of such processes.
Yet another object of the present invention is to provide an improved process for exhaustion of titanium dioxide onto a polyester textile material to improve opacity of the material without adversely affecting handle of the material and to provide improved products produced thereby.
A further object of the present invention is to provide a polyester fiber-containing textile material which not only has improved opacity characteristics on a per unit titanium dioxide add-on basis as compared to known products but which also is easier to clean and which "hides" the presence of soil on the fabric.
Generally speaking, the present invention relates to polyester fiber-containing textile material having improved opacity and handle characteristics, which comprises a polyester fiber-containing substrate; sald textile fibers having been covered with titanium dioxide particles having an average par ticle size of at least about 0.1~ micron in an amount of up to , .
~ -4-about 20 percent by weight, the durability of bonding of said particles to said textile fibers in the absence of a binder as the primary bonding means being such that at least about 50 per-cent of said particles remain bound to the surface of said textile fibers after five standard washings according to the standards set by the American Association of Textile Chemists and Colorists (herein AATCC). Furthermore, according to the inven-tion and as can be observed in the attached photographs the particles will be disposed on the textile material so as not to form a substantial number of agglomerates of the particles be-tween the textile fibers.
The present invention also relates to an improved process for rendering a polyester fiber-containing textile material more opaque comprising the steps of providing an aqueous dispersion lS of titanium dioxide pigment having a particle size of at least about 0.18 micron; contacting said textile material with said aqueous dispersion under agitation conditions and at a pH below approximately 7.5 whereby said pigment exhausts from said disper-sion onto said textile material, and thereafter heat setting the textile material.
The polyester fiber-containing textile material of the present invention may be in a yarn or filament form, a woven or knitted fabric form, a non-woven form or the like. The textile material may contain at least about 10 percent by weight, pre-ferably at least about 40 percent by weight, polyester fibers.All polyester textile materials, especially 100 percent textured polyester, have been found to be particularly suitable as textile substrates in the products of the present invention.
The titanium dioxide particles of the present invention may be in pigment form, may be of either rutile or anatase crystalline structure and may have alumina or silica coatings thereon. The thrust of the present invention is, of course, to provide a polyester textile material having improved opacity.
As such, the particle size of the titanium dioxide pigment should be at least about 0.18 micron, whereby improved covering power of the textile material is likewise realized coincident with the opacity characteristic. Hence, the titanium dioxide suitable for use according to the present invention must be of sufficient particle size to create a whitening effect on the textile material. Up to about 7 percent titanium dioxide particles based on the textile material weight may be provided on the tex-tile material without any substantial "dusting" and with good dura-bility to laundering and dry cleaning, even in the absence ofeven a minor amount of an extraneous adhesive binder. Amounts of titanium dioxide ranging up to about 20 percent based on the weight of the material may be provided with only slight "dusting"
in the total absence of an adhesive binder; and where it is de-sired to provide such larger amounts of pigment, a minor amountof binder, e.g., about 2 percent or less by weight, may be applied as a secondary bonding means to minlmize or eliminate "dusting"
and to further improve the durability to laundering and dry cleaning.
The process of the present invention is preferably directed ~' to dispersing titanium dioxide pigment in an aqueous medium having a basic pH whereby the dispersion remains stable in the absence of agitation. The polyester fiber-containing textile material is con-tacted by the aqueous dispersion with relative agitation between ~L~
the dispersion and the textile material. After the textile material is in the dispersion under agitation conditions, pH of the dis-persion is gradually reduced to a level below approximately 7.5 at which point the pigment begins to exhaust from the dispersion onto the textile material. Completion of exhaustion of the pig-ment from the bath is evidenced by clarification of the bath, While in the preferred process embodiment the pH of the dispersion may be graudally reduced by any means exemplified by controlled addition of acid or the in situ generation of acid, preferably an acid generating compound is added to the dispersion which requires some extrinsic means for yeneration of the acid.
Utilization of acid generating compounds permits a safer operation with better control of pH reduction of the bath. In a most pre-ferred situation, an acid generating substance, such as butyro-lactone, is included in the dispersion which, when heatedgenerates acid and gradually lowers pH of the dispersion.
In a most preferred embodiment, titanium dioxide pigment having a particle size of approximately 0.2 micron is dispersed in an aqueous medium with an ala~li to achieve approxim~tely 5 percent titanium dioxide based on weight of the textile material and a bath pH of approximately 9, The textile material is then contacted with the dispersion under continuous relative agitation conditions and butyrolactone, dyestuff and dye auxiliaries are added to the bath. Temperature of the bath is then gradually raised at a rate of approximately 3F. per minute to approximately 266F. with pH of the dispersion being gradually reduced to about 4.7. As the acid is produced and pH is lowered below about 7.5, the titanium dioxide begins to exhaust onto the textile material, .
~7--Upon reachlng a pH of 4.7 and a bath temperature of 266F., the dispersion becomes clear, indicating almost complete exhaustion of titanium dioxide therefrom. The textile material having the titanium dioxide thereon is then removed from the bath, rinsed, dried and heat set. The titanium dioxide, for all practical purposes, is durably bonded to the textile material, even in the absence of an extraneous adhesive binder as the primary bonding means. The textile material is thus rendered more opaque at an approximate pick up of, for instance, 5 percent by weight titanium dioxide, with little change to the handle of the fabric. The textile material may then be further processed to render same soil resistant, crease resistant, or the like without any adverse change to the durability of the titanium dioxide thereon. It will also be apparent that although no extraneous adhesive binders are required to provide a durable bond, minor amounts, e.g., about
Adhesive binders, and titanium dioxide, either in the form of a titanium salt or a pigment, have heretofore been present in dispersions, solutions or emulsions along with other ingredients and brought into contact with the textile material for normal application thereto. The textile material was thereafter further processed to promote adherence of the various ingredients thereto.
.~ ~
It has further been known to utilize titanium salts in dispersions that are applied to textile materials, such as cellulose acetate, rayon and the like to deluster same. Appli-cation of the metal oxides to deluster a cellulosic substrate has - 5 conventionally utilized a metal salt in the dispersion with the salt thereafter being acid treated to release the metal ions which become affixed to the substrate under acidic conditions. In fact, such processes have historically been operated totally under acid conditions. Other techniques have likewise been utilized for applying titanium dioxide onto textile materials. Exhaustion techniques have been practiced, where the particle size of the titanium dioxide was 0.1 micron or smaller. In such processes, the titanium dioxide is of such particle size as to be colorless and is applied to resist soiling of the textile material without any whitening effect. In other wordsl opacity is not improved.
While all of the above techniques have in fact been pre-viously utilized to apply titanium dioxide and other metal oxides onto textile substrates, no one or combination of same has approached the problem of the present inventi~on, i.e., providing an improved polyester fiber-containing textile material which has been rendered more opaque to the passage of light wherein the material added to improve the opacity is bound to the substrate without the necessity of an adhesive binder as the primary means for bonding the particles to the surface of the textile material, and yet is quite durable to repeated laundering and dry cleaning operations, and compatible with other textile ~inishing opera-tions. Very importantly, relatively large amounts of pigment may be added to the textile substrate without a resultant harsh handle.
It is an object of the present invention to provide a polyester fiber-containing textile material having improved opa-city and to provide a process for preparing same.
-Another object of the present invention is to provide improved polyester fiber-containing textile materials which are more opaque to the transmission of light and which have good handle characteristics and to provide a process for preparing same.
Still another object of the present invention is to pro-vide a process for the adhesion of titanium dioxide to a poly-ester textile material from a bath in the absence of a binder asthe primary means of adhesion and to provide products of such processes.
Yet another object of the present invention is to provide an improved process for exhaustion of titanium dioxide onto a polyester textile material to improve opacity of the material without adversely affecting handle of the material and to provide improved products produced thereby.
A further object of the present invention is to provide a polyester fiber-containing textile material which not only has improved opacity characteristics on a per unit titanium dioxide add-on basis as compared to known products but which also is easier to clean and which "hides" the presence of soil on the fabric.
Generally speaking, the present invention relates to polyester fiber-containing textile material having improved opacity and handle characteristics, which comprises a polyester fiber-containing substrate; sald textile fibers having been covered with titanium dioxide particles having an average par ticle size of at least about 0.1~ micron in an amount of up to , .
~ -4-about 20 percent by weight, the durability of bonding of said particles to said textile fibers in the absence of a binder as the primary bonding means being such that at least about 50 per-cent of said particles remain bound to the surface of said textile fibers after five standard washings according to the standards set by the American Association of Textile Chemists and Colorists (herein AATCC). Furthermore, according to the inven-tion and as can be observed in the attached photographs the particles will be disposed on the textile material so as not to form a substantial number of agglomerates of the particles be-tween the textile fibers.
The present invention also relates to an improved process for rendering a polyester fiber-containing textile material more opaque comprising the steps of providing an aqueous dispersion lS of titanium dioxide pigment having a particle size of at least about 0.18 micron; contacting said textile material with said aqueous dispersion under agitation conditions and at a pH below approximately 7.5 whereby said pigment exhausts from said disper-sion onto said textile material, and thereafter heat setting the textile material.
The polyester fiber-containing textile material of the present invention may be in a yarn or filament form, a woven or knitted fabric form, a non-woven form or the like. The textile material may contain at least about 10 percent by weight, pre-ferably at least about 40 percent by weight, polyester fibers.All polyester textile materials, especially 100 percent textured polyester, have been found to be particularly suitable as textile substrates in the products of the present invention.
The titanium dioxide particles of the present invention may be in pigment form, may be of either rutile or anatase crystalline structure and may have alumina or silica coatings thereon. The thrust of the present invention is, of course, to provide a polyester textile material having improved opacity.
As such, the particle size of the titanium dioxide pigment should be at least about 0.18 micron, whereby improved covering power of the textile material is likewise realized coincident with the opacity characteristic. Hence, the titanium dioxide suitable for use according to the present invention must be of sufficient particle size to create a whitening effect on the textile material. Up to about 7 percent titanium dioxide particles based on the textile material weight may be provided on the tex-tile material without any substantial "dusting" and with good dura-bility to laundering and dry cleaning, even in the absence ofeven a minor amount of an extraneous adhesive binder. Amounts of titanium dioxide ranging up to about 20 percent based on the weight of the material may be provided with only slight "dusting"
in the total absence of an adhesive binder; and where it is de-sired to provide such larger amounts of pigment, a minor amountof binder, e.g., about 2 percent or less by weight, may be applied as a secondary bonding means to minlmize or eliminate "dusting"
and to further improve the durability to laundering and dry cleaning.
The process of the present invention is preferably directed ~' to dispersing titanium dioxide pigment in an aqueous medium having a basic pH whereby the dispersion remains stable in the absence of agitation. The polyester fiber-containing textile material is con-tacted by the aqueous dispersion with relative agitation between ~L~
the dispersion and the textile material. After the textile material is in the dispersion under agitation conditions, pH of the dis-persion is gradually reduced to a level below approximately 7.5 at which point the pigment begins to exhaust from the dispersion onto the textile material. Completion of exhaustion of the pig-ment from the bath is evidenced by clarification of the bath, While in the preferred process embodiment the pH of the dispersion may be graudally reduced by any means exemplified by controlled addition of acid or the in situ generation of acid, preferably an acid generating compound is added to the dispersion which requires some extrinsic means for yeneration of the acid.
Utilization of acid generating compounds permits a safer operation with better control of pH reduction of the bath. In a most pre-ferred situation, an acid generating substance, such as butyro-lactone, is included in the dispersion which, when heatedgenerates acid and gradually lowers pH of the dispersion.
In a most preferred embodiment, titanium dioxide pigment having a particle size of approximately 0.2 micron is dispersed in an aqueous medium with an ala~li to achieve approxim~tely 5 percent titanium dioxide based on weight of the textile material and a bath pH of approximately 9, The textile material is then contacted with the dispersion under continuous relative agitation conditions and butyrolactone, dyestuff and dye auxiliaries are added to the bath. Temperature of the bath is then gradually raised at a rate of approximately 3F. per minute to approximately 266F. with pH of the dispersion being gradually reduced to about 4.7. As the acid is produced and pH is lowered below about 7.5, the titanium dioxide begins to exhaust onto the textile material, .
~7--Upon reachlng a pH of 4.7 and a bath temperature of 266F., the dispersion becomes clear, indicating almost complete exhaustion of titanium dioxide therefrom. The textile material having the titanium dioxide thereon is then removed from the bath, rinsed, dried and heat set. The titanium dioxide, for all practical purposes, is durably bonded to the textile material, even in the absence of an extraneous adhesive binder as the primary bonding means. The textile material is thus rendered more opaque at an approximate pick up of, for instance, 5 percent by weight titanium dioxide, with little change to the handle of the fabric. The textile material may then be further processed to render same soil resistant, crease resistant, or the like without any adverse change to the durability of the titanium dioxide thereon. It will also be apparent that although no extraneous adhesive binders are required to provide a durable bond, minor amounts, e.g., about
2 percent or less by weight of an extraneous adhesive binder may be applied to the material to further enhance the durability of bonding of the particles to the textile substrate. ~enerally, however, even where an adhesive binder is applied the amount required will be minor so that the handle of the material may not be so adversely affected as to render the material undesirable for its intended applications.
The polyester fiber-containing textile material of the present process may be characterized as approximately twice as opaque as untreated controls. For example, utilizing a ~unter Color Difference Meter, samples are measured for reflection (L value~ over both a white and a black background, and then opacity is expressed as the difference in L values (~L). A
completely transparen-t sample exhibits a ~L value of 100 while a totally opaque sample exhibits a ~L value of 0. Hence, poly-ester fiber-containing materials treated by the present process exhibit approximately one half the ~L as that of the untreated control. secause the titanium dioxide particles are bonded to the material surface in the absence of a binder as the primary bonding means, improved opacity is accomplished without adversely affecting the handle characteristics of the material.
In general, it has been determined that the titanium dioxide particles of the textile material product of the present invention will coat from about 2 percent to about 80 percent, preferably about 10 percent to about 40 percent, of the surface of the tex-tile material. Coating may be determined quantitatively based upon examination of electron micrographs of a textile material.
If no particles are bound to the surface and the surface is sub-stantially free of pigment particles the extent of coating is 0.
If the textile material is completely covered with particles and no fiber substrate is visible on an electron micrograph the extent of coating is 100 percent, although as a practical matter such a high level of coating would probably not be required in a textile material product. Similarly, if about half of the fiber sub-strate is visible on a micrograph the extent of coating is 50 percent, and so forth.
Generally, the products of the present invention exhibit substantially improved cover as compared to prior art products based upon the same amount of titanium dioxide by weight, pro-vided on the surface of the product. This improvement, which is quite surprising, is achieved, it is thought, because the pigment _9_ ~X
particles are in general much more evenly distributed on the surface of the textile material of the present invention than in known textile products. While this even distribution is difficult to quantify or even descri~e verbally it is quite apparent visually as can be seen by the side by side comparison provided in the attached micrographs. Thus, Figures 1-3 illustrate magnifi-cations of the products of the present invention of 470X, 950X
and l900X using the process and employing the same materials set forth in Example l except that the pigment was Titanox 1070 manufactured by NL Industrties. The even distribution of the particles on the surface of the textile material is quite apparent and is even more apparent when compared with Figure 4 which illustrates the prior art padding technique using the same pig-ment with about 5 percent titanium dioxide applied based on the weight of the fabri_. The pigment was padded on, dried and cured.
Figure 4 which is approximately the same magnification as Figure 1 shows that there has been a substantial amount of agglomeration of the particles, and this agglomeration is particularly apparent at the interfaces of the fibers with one another. By contrast in Figures l to 3, agglomeration of the particles has been minimized, with the average agglomerate size being less than about 25 primary particles. While Figures 1 to 3 are illustrations of products made in the laboratory under ideal conditions (as in the product illustrated in Figure 4) even in production conditions agglomeration of the particles on the surface of the products of the invention (illustrated in Figures 5 and 6 at magnifications of 950X and l900X) is certainly minimized, with average agglo-merate sizes being generally less than about 50 primary particles per agglomerate although somewhat higher average agglomerate sizes may be observed in certain applications. Also, the average agglomerate size may vary depending upon the definition of what constitutes an agglomerate. In any event, it is though that the "minimization of agglomeration" feature of the present invention is very apparent based upon visual observation of the attached micrographs. Minimization of agglomeration, furthermore, remains as a characteristic of the product even after subsequent finishing as illustrated in Figures 7 and 8 at magnifications of 450X and 1900X.
In addition to the improved cover, opacity, and handle characteristics of the products of the present invention, perhaps most importantly it has been observed that the titanium dioxide particles of the present invention are very durably bonded to the surface even in the absence of a binder as the primary bonding means, although minor amounts of an extraneous adhesive binder may be present in the product as a secondary bonding means where desired. Applicant has not been able to determined precisely how such advantageously durable bonding is accomplished, it being sufficient to state that the particles are adhered durably to the surface of the textile material. Thus, the bond that is formed is durable in the absence of a binder as the primary bonding means;
and this durability characteristic may be measured by subjecting the textile products to standard AATCC washings. This standard AATCC washing is described in Method 130, Procedure 2, of the Technical Manual of the American Association of Textile Chemists and Colorists, Vol. 53, p. 253 (1978 ed.), and will be well-known to those skilled in the textile arts. While it will be appre-ciated that durability of bonding will depend upon such factors as the amount of TiO2 initially applied, method of application, substrate composition, and the presence on the material of binders and other additives, generally, the products of the present invention may be characterized in that at least about 50 percent, preferably about 70 percent or more by weight, of the titanium dioxide particles remain bound to the surface of the textile fibers after five standard AATCC washings. In certain preferred applications the durability of bonding may be even greater, e.g., about 80 percent or even greater after five AATCC
washings The textile material products of the present invention may be further characterized by certain additional advantageous properties in a textile product. For instance, the products generally exhibit improved "flat dry" characteristics as compared to known products where a binder is generally employed as the primary means of bonding the particles to the textile material.
The products of the present invention also exhibit improved moisture wicking properties as compared to known products. The soil release characteristics of the products of the present in-vention are also significantly improved by application of any of the known soil release agents as compared to known products of the same type where a binder has been employed since the proper-ties of most or all known binders in general are disadvantageous from a soil release standpoint.
Preferred embodiments of the process of the present in-vention will now be described in detail. In the context of the present invention, polyester fiber-containing textile materials that may be treated to provide a product having improved opacity may be a spun yarn, an extruded filament, a woven fabric, a knitted fabric, an unwoven web, or the like. Obviously, in the sense of strands such as spun yarns or extruded filaments, opacity will be apparent per se and will carry forward to a substrate formed therefrom, e.g., by weaving, knitting, non-woven techniques or the like. Extruded filaments per se or in fabric or web form may have a ro~md cross section, or preferably, may possess a non-round cross section such as multilobal, and are preferably texturized.
The terms "textured" and "texturized" are used herein interchangeably to refer to an otherwise smooth, continuous fila-mentary yarn which has been crimped, looped, coiled, or crinkled by any one of at least a dozen well-known techniques to impart mproved properties thereto, such as stretch, luxurious bulk, greater absorbency and/or improved hand. The most preferred texturized yarns of the invention are those made by false twist-ing of the yarn on any of the well-known and used false-twist .
type stretch yarn machines, such as those made by ARCT, Barmag, Berliner, Davide, Guidici and others. Among the many advantages of fabrics made from texturized yarns, particularly polyester yarns, are that they simulate some of the characteristics of fabrics made from spun yarns and provide certain additional ad-vantageous characteristics such as improved pill and crease resistance, better shape retention, great~r durability and more uniform appearance.
In the context of the present invention, the term poly-ester fiber means any polymeric ester that has been extruded into filamentary form. Conventionally, the polyester is the reaction . ~ i product of a dicarboxylic acid, or ester forming derivative of same and a glycol, e.g., dimethyl terephthalate and ethylene glycol that is condensed to provide a polymer of the glycol ester of the dicarboxylic acid. Such polyester may also contain other constituents to render the filaments extruded therefrom capable of basic dyeability, to impart antlstatic properties, flame re-tardant properties or the like.
In applying the titanium dioxide, which as indicated above should have an average particle size of at least about 0.18 micron, a good dispersion can be attained under alkaline conditions, which will remian stable for prolonged periods of time. As the pH of the dispersion is changed to the acid side, the titanium dioxide begins to exhaust therefrom. Gradual lowering of the pH of the dispersion achieves a quite uniform application of titanium dioxide onto the textile material. In fact, it was totally sur-prising to determine that relatively large amounts of titanium dioxide can be exhausted onto the textile material by the present techniques while retaining a good material handle for garment end use. Likewise, it was surprising to determine that the pigment is durable to repeated laundering and dry cleaning without the use of adhesive binders as the primary means for bonding the particles to the surface of the textile material.
When an initial dispersion has an acid pH, agitation is required to maintain proper dispersion stability, Likewise, uniformity of deposition of the titanium dioxide pigment appears less than when the initial dispersion has a basic pH, ~ . . . . .
While not wlshing to be bound by any particular theory, it is hypothecated that the titanium dioxide pigment begins to ex-haust from the dispersion at its isoelectric point where the electrical charge on the titanium dioxide particles changes from negative to positive. In any event, when the pH of the disper-sion becomes about 7.5 or below, exhaustion commences. A gradual reduction of pH of the dispersion permits the pigment to adhere to the textile material as it exhausts from the dispersion with little or no pigment precipitation from the bath. Too rapid a reduction of pH interferes with uniform application of pigment onto the substrate and tends to destroy stability of the dis-persion.
A proper dispersion of titanium dioxide pigment in water may be obtained by any suitable procedure. For example, for the preferred embodiment the pigment may be predispersed in a dilute alkaline solution, or may be added directly to the alkaline aqueous medium. Suitable alkaline materials include without limitation, ammonium hydroxide, sodium hydroxide and the like.
Thereafter, stirring will disperse the pigment in the medium as evidenced by a milky appearance, and the dispersion will remain stable. According to the present invention, the amount of titanium dioxide pigment in the dispersion may be in a range of from about 1.0 to about 20 weight percent based on the weight of textile material to be treated~ and preferably about 3 to about 7 percent. Up to 7 percent titanium dioxide based on material weight has been added to a textile material without "dusting" and with good durability to laundering and dry cleaning. In like vein, amounts of about 20 percent based on material weight have beed added with only slight "dusting."
During operation of the present proce~s, it is most de-sirable to maintain continuous relative movement between the dispersion and the textile material. Such may be accomplished by continuous agitation of the dispersion or movement of the textile material, or both. Since, as mentioned hereinafter, the present process is compatible with dyeing operations, the process may be conducted in commercial dyeing apparatus such as a jet rope dyeing apparatus where the textile material is handled in rope form, agitated by a jet of water or the like.
Once the substrate is in contact with the dispersion, the pH can then be lowered to promote the exhaustion. While any technique may be employed for lowering the pH of the dispersion, as mentionled above, the drop should be gradual. An acid, e.g., acetic acid, may be slowly added to the dispersion to lower the pH. At a pH above 4, it is preferable to heat the dispersion for complete exhaustion, while at a pH of 4 or below complete ex-haustion of the titanium dioxide will occur at ambient temperature.
A preferred technique, however, for adjustment of the dispersion pH is the addition of an acid generating compound which, when subjected to a predetermined condition, such as the application of heat, will liberate an acid which in turn lowers the pH of the dispersion. Butyrolactone, a compound marketed under the name SANDACID V by Sandoz Chemical Company is a preferred acid generating compound. Temperature increase is con-trolled to limit acid generation and, therefore, achieve thegradual pH reduction.
Though no ingredients are essential to operation of the present process other than those to disperse titanium dioxide in an aqueous medium and a means for adjusting pH of the dispersion, other ingredients may be included in the dispersion so long as they do not adversely affect exhaustion of the titanium dioxide, handle of the material for its intended use, durability of the treatment, or the like. Without limitation, such further ingred-ients which may or may not be present in sizable quantitiesinclude dyestuffs, dyestuff carriers, levelers, lubricants, chelating agents, optical brighteners, binders in a minor amount, and the like. In like fashion, after improving the opacity or cover of a textile material according to the process of the present invention, the textile material may thereafter be treated to impart crease resistant properties, soil resistant properties, fire retardant properties, and the like thereto. In fact, the present process may be conducted simultaneously with a soil re-lease or soil resistant treatment, though same is not preferred.
In general, whether the initial dispersion is alkaline or acid, exhaustion of the titanium dioxide occurs at a pH below about 7.5. As mentioned above, a preferred process utilizes an initially alkaline dispersion with the pH of same being gradually reduced to the acid side. Such produces a very uniform deposition of titanium dioxide on the substrate. Preferably, whether intially alkaline or acid, p~I of the dispersion during exhaustion falls in a range of from about 6 to about 3, with a most preferred range being from about 5 to about 4.
While the titanium dioxide applied to the polyester textile material is durable without other ingredients, subsequent appli-cations of crease resistant chemicals, soil resistant chemicals, or, as mentioned above a minor amount of an extraneous adhesive binder and the like, will add further durability. Likewise, the polyester textile material may be heat set after the titanium B~3 dioxide is added to further enhance durability. Heat setting, for example, will cause a substantially greater amount of titanium dioxide to be retained on the substrate after repeated washings and dry cleanings. Normally the heat settiny is con-ducted by subjecting the material to temperature in a range offrom about 300 to about 400F. for a residence time of from about 5 seconds to about 2 minutes. As mentioned above, while an ex-traneous adhesive binder is ordinarily not required to provide a product having good durability, a minor amount, e.g., about 2 percent or less by weight of an adhesive binder, may be applied to the material where desired.
The process according to teachings of the present in-vention may be better understood by reference to the following examples Example 1 A length of 100 percent texturized polyester fabric was placed in a Mathis laboratory dyeing apparatus, type JF. Water was then introduced into the dyeing apparatus at a temperature of 80F. adequate to provide a bath to fabric weight ratio of 30:1, and agitation started. Titanium dioxide pigment (TI-Pure 960 manufactured by DuPont) was predispersed in a dilute ammonium hydroxide solution in a Waring blender for five minutes. There-after, the titanium dioxide-ammonium hydroxide dispersion was added to the aqueous bath in the dyeing apparatus to an amount of pigment representing 5 percent of the weight of fabric, and pH of the bath was 9Ø After agitation for five further minutes, butyrolactone (SANDACID* V manufactured by Sandez Chemical Company) was added to the dispersion in an amount of 3 percent *Trademark X
~L~ 3 based on fabric weight. Temperature of ~he dlspersion was then raised at a rate of 3F. per minute to a temperature of 266F.
The 266F. temperature was held for five minutes after which the bath was cooled to 160F. Bath pH then measured 4.7, and ex-hibited clarity, indicating exhaustion of the pigment. Thefabric was then removed from the bath, rinsed once, dried and heat set at a temperature of 350F. for one minute. The processed fabric exhibited greatly improved opacity when compared to a con-trol fabric that was processed in like fashion without the presence of the titanium dioxide pigment. Weight an~lysis in-dicated that 95 percent of the titanium dioxide had exhausted from the dispersion onto the fabric. Improved opacity remained after repeated laundering and dry cleaning, evidencing durability, About-70 percent of the titanium dioxide particles remained after 5 AATCC washings.
Example 2 A length of 100 percent texturized polyester fabric was placed in a beaker of cold water with a water to fabric ratio of ` 30:1 and agitated. Ammonium hydroxide was then added to the bath adequate to bring the pH of the bath to 10Ø Titanium dioxide pigment was then added to the bath in an amount equivalent to 7 percent based on weight of the fabric (particle size 0.22 micron). Agitation was continued for five minutes after which pH of the bath was adjusted to 4.0 with the prolonged gradual addition of acetic acid. Temperature of the bath was then gradually raised to 212F. At a temperature of approximately 158F., appreciable exhaustion of the titanium dioxide pigment was noted. After fifteen minutes at 212F., the bath was clear 8~C)3 indicating almost complete exhaustlon of the titanium dioxide.
The fabric was removed from the bath, dried and cured at a temperature of 360F. for 30 seconds and weighed whereupon it was determinéd that 95 percent of the titanium dioxide pigment had exhausted onto the fabric. The fabric exhibited improved opacity which was durable to both laundering and dry cleaning.
Virtually no "dustinq" was noted, and a good fabric handle was apparent. About 70 percent of the titanium dioxide particles remained after 5 AATCC washings.
Example 3 _ The procedure of Example 2 was repeated with the excpetion that temperature of the bath was maintained at ambient conditions.
Again, virtually all the titanium dioxide exhausted onto the textile fabric, and improved, durable opacity resulted, though a longer period of time was required for complete exhaustion.
About 60 percent of the titanium dioxlde particles remained after 5 AATCC washings.
Example 4 Textured polyester fabric was processed as described in Example 1. The processed sample was then evaluated along with an untreated control to determine the initial opactiy of same and durability of opacity after repeated washing at 120F. for five minutes. Opacity was determined with a Hunter Color Difference Meter as discussed above. The value for ~ L indicates the degree of opacity ranging from 0 for total opacity to 100 for complete transparency. Results are set forth in Table I.
TABLE I
OPACITY OF TEXTURED POLYESTER FABRICS
Untreated I'iO
Control on Fahric, Heat Set Initial Opacity, ~ L 14.2 5.8 After 1 Wash, ~ L 14.0 6.7 After 5 Washes, ~ L 14.0 6.8 After 10 Washes, ~ L 13.9 7.0 After 20 Washes, ~ L 13.9 7.0 After 50 Washes, ~ L 13.9 7.3 Example 5 Fabric samples processed as set forth in Example 1, certain of which were not heat set, were subjected to up to 5 home laundering operations, during which titanium dioxide count was intermittently checked to further determine the durability of the titanium dioxide on the substrate. Results are indicated in Table II.
TABLE II
TiO2 Count Sample Initial After l Wash After 5 Washes Heat Set 684 542 420 Not Heat Set 765 282 177 Titanium dioxide count indicates the amount of titanium dioxide on the substrate and is a measure of intensity, corrected for background in counts per second determined by x-ray fluorescence. It is thus noted that durability is enhanced by heat setting, and with heat setting, appreciable amounts of titanium dioxide remain after repeated washings.
Example 6 Texturized 100 percent polyester was processed as described in Example 1 with the exception that the fabric was only dried and was not heat set. Thereafter, the fabric with the titanium dioxide thereon was padded with an emulsion containing a copoly-mer of methyl acrylate: acrylic acid (70:30) to provide 0.3 percent copolymer solids based on fabric weight. me fabric was then dried and heat set at 350F. for one minute. Good durable cover was found to be present for the fabric along with good soil release properties. About 70 percent of the titanium dioxide particles remained after 5 AATCC washings.
Example 7 Example 1 was repeated with the exception that a pink dispersed dyestuff was also incorporated into the bath to achieve 0.1 percent dyestuff based on fabric weight. The fabric ex-hibited improved opacity as with Example 1, and was dyed an even pink color. The fabric was subjected to repeated laundering and dry cleaning operations, and was durable both as to dye level and cover.
Example 8 As mentioned above, it is known that titanium salts may be used in dispersions that are applied to textile materials, such as cellulose acetate, rayon and the like to deluster same.
In such exhaustion techniques, which represent the closest prior .~ .
~ . . . . . .
8~ 3 art known to applicant at the time of filing of the application, the particle size of the titanium dioxide is generally 0.1 micron or smaller. Furthermore, the products of the present invention exhibit markedly improved physical characteristics as compared to products produced by such prior art exhaustion techniques, and Table III below illustrates the novel characteristics of the products of the present invention (see column 2) as compared to a control sample of the same fabric substrate to which no titanium dioxide particles have been applied (column 1). The same pro-cedure was follows to prepare the sample illustrated in column2 that is set forth in Example 1 except that the pigment used was Titanox 1070, an anatase product manufactured by NL Industries.
A sample of the same fabric treated by a known exhaustion tech-nique, namely Example 1 of U. S. Patent No. 2,309,294 (herein the '294 patent), wherein the titanium dioxide particles of the same type used to prepare the sample of column 2 were exhausted from a bath containing aluminum formate is illustrated in column 3. Column 4 shows the physical characteristics of the same substrate treated by padding according to the process of Example 2 of the '294 patent. Column 5 provides the physical characteristics of the same substrate processed again according to Example 1 except that the bath contalned aluminum sulfate rather than aluminum ~ormate. In the Table the designation P
stands for poor, F-G stands for fair to good, G stands for good, VG stands for very good, and E stands for excellent.
~B~3 TABLE I I I
Without Soil Release Finish Product Aluminum 294 2 Aluminum Characteristics Control Invent~on Formate Padded Sulfate -Cover P E P F~G F
5 Durability of Cover - G P P P
Hand G G G P F-G
Moisture Transport P E P P P
Crocking - VG VG P P
Agglomeration - Slight Medium ~eavy Medium 10 Soil Hiding P G P F-G F
% Exhaustion - 80 20 - 50 Example 9 In this Example the same samples used in Example 8 and Table III were all padded according to the procedure set forth in Example 6 with a soil release emulsion containing a copolymer of methyl acrylate: acrylic acid (7Q:30), an ethoxylated poly-ester and a lubricant (ethoxylated oleic acid) to provide 0~3 percent copolymer solids, 0.15 percent ethoxylated polyester and 1.0 percent lubricant based on the fabric weight. The re-~0 sulting properties of the textile materials are set forth belowin Table IV:
X
. .
TABLE IV
With Soil Release E~inish Aluminum 294 2 Aluminum Control "CUMULUS" Format'e Padded Sulfate Cover P E P F F
5 Durability of Cover - G P P P
Hand G G G P F
Soil Release G G G G G
Moisture Transport G E G G G
Crocking - VG VG P P
10 Agglomeration - SlightMedium Heavy Medium Soil Hiding P G P F-¢ F
~ Example 10 : Example 1 was repeated on a length of 100 percent spun polyester woven fabric instead of texturized polyester. The processed fabric exhibited greatly improved opacity ( ~ L value of 9.1) when compared to a control fabric that was processed in like fashion without the presence of the titanium dioxide pigment ( ~ L value of 18.3). Improved opacity remained after repeated launderings ( ~ L value of 13.0 after 5 washings as compared to ~ L value of 18.2 for the control fabric).
Example 11 Example 1 was repeated again on a length of 100 percent filament (untexturized) polyester woven fabric instead of the texturized polyester of Example 1. The processed fabric exhibited ~.
.
.
greatly improved opacity ( ~ L value of 17.0) when compared to a control fabric that was processed in like fashion without the presence of titanium dioxide pigment ( ~ L value of 28.5).
~ Example 12 Example l was repeated once more on a length of nylon taffeta fabric instead of the lO0 percent texturized polyester fabric of Example l. While the processed fabric exhibited some improved opacity initially ( ~ L value of ll.9) as compared to a control fabric that was processed in like fashion without the presence of titanium dloxide pigment ( ~ L value of 24.5) after only 5 standard washings only about 8.7 percent of the particles initially present on the fabric remained.
Example l3 Example l was repeated on a length of lO0 percent woven acrylic fabric instead of the texturized polyester of Example l.
While the processed fabric exhibited some improved opacity initially ( ~ L value of 3.2) as compared to the control fabric that was processed in a like fashion without the presence of titanium dioxide pigment ( ~ L value of 15.0) af-ter only 5 standard washings only about 25 percent of the particles initially present on the fabric remained.
Example 14 Example l was repeated on a length of 65/35 polyester/
cotton blend woven fabric instead of the lO0 percent texturized polyester of Example l. While the processed fabric exhibited some improved opacity initially ( ~ L value of 6.2) as compared to a control sample that was processed in a like fashion without ~ .
the presence of titanium di.oxide pigment ( ~ L value of 16.0) after only 5 standard washings only about 24 percent remained on the fabric. The ~ L value after 5 washings of the treated sample was 10.2, however, which compared favorably even against the ini.tial opacity of the control sample.
X
.
The polyester fiber-containing textile material of the present process may be characterized as approximately twice as opaque as untreated controls. For example, utilizing a ~unter Color Difference Meter, samples are measured for reflection (L value~ over both a white and a black background, and then opacity is expressed as the difference in L values (~L). A
completely transparen-t sample exhibits a ~L value of 100 while a totally opaque sample exhibits a ~L value of 0. Hence, poly-ester fiber-containing materials treated by the present process exhibit approximately one half the ~L as that of the untreated control. secause the titanium dioxide particles are bonded to the material surface in the absence of a binder as the primary bonding means, improved opacity is accomplished without adversely affecting the handle characteristics of the material.
In general, it has been determined that the titanium dioxide particles of the textile material product of the present invention will coat from about 2 percent to about 80 percent, preferably about 10 percent to about 40 percent, of the surface of the tex-tile material. Coating may be determined quantitatively based upon examination of electron micrographs of a textile material.
If no particles are bound to the surface and the surface is sub-stantially free of pigment particles the extent of coating is 0.
If the textile material is completely covered with particles and no fiber substrate is visible on an electron micrograph the extent of coating is 100 percent, although as a practical matter such a high level of coating would probably not be required in a textile material product. Similarly, if about half of the fiber sub-strate is visible on a micrograph the extent of coating is 50 percent, and so forth.
Generally, the products of the present invention exhibit substantially improved cover as compared to prior art products based upon the same amount of titanium dioxide by weight, pro-vided on the surface of the product. This improvement, which is quite surprising, is achieved, it is thought, because the pigment _9_ ~X
particles are in general much more evenly distributed on the surface of the textile material of the present invention than in known textile products. While this even distribution is difficult to quantify or even descri~e verbally it is quite apparent visually as can be seen by the side by side comparison provided in the attached micrographs. Thus, Figures 1-3 illustrate magnifi-cations of the products of the present invention of 470X, 950X
and l900X using the process and employing the same materials set forth in Example l except that the pigment was Titanox 1070 manufactured by NL Industrties. The even distribution of the particles on the surface of the textile material is quite apparent and is even more apparent when compared with Figure 4 which illustrates the prior art padding technique using the same pig-ment with about 5 percent titanium dioxide applied based on the weight of the fabri_. The pigment was padded on, dried and cured.
Figure 4 which is approximately the same magnification as Figure 1 shows that there has been a substantial amount of agglomeration of the particles, and this agglomeration is particularly apparent at the interfaces of the fibers with one another. By contrast in Figures l to 3, agglomeration of the particles has been minimized, with the average agglomerate size being less than about 25 primary particles. While Figures 1 to 3 are illustrations of products made in the laboratory under ideal conditions (as in the product illustrated in Figure 4) even in production conditions agglomeration of the particles on the surface of the products of the invention (illustrated in Figures 5 and 6 at magnifications of 950X and l900X) is certainly minimized, with average agglo-merate sizes being generally less than about 50 primary particles per agglomerate although somewhat higher average agglomerate sizes may be observed in certain applications. Also, the average agglomerate size may vary depending upon the definition of what constitutes an agglomerate. In any event, it is though that the "minimization of agglomeration" feature of the present invention is very apparent based upon visual observation of the attached micrographs. Minimization of agglomeration, furthermore, remains as a characteristic of the product even after subsequent finishing as illustrated in Figures 7 and 8 at magnifications of 450X and 1900X.
In addition to the improved cover, opacity, and handle characteristics of the products of the present invention, perhaps most importantly it has been observed that the titanium dioxide particles of the present invention are very durably bonded to the surface even in the absence of a binder as the primary bonding means, although minor amounts of an extraneous adhesive binder may be present in the product as a secondary bonding means where desired. Applicant has not been able to determined precisely how such advantageously durable bonding is accomplished, it being sufficient to state that the particles are adhered durably to the surface of the textile material. Thus, the bond that is formed is durable in the absence of a binder as the primary bonding means;
and this durability characteristic may be measured by subjecting the textile products to standard AATCC washings. This standard AATCC washing is described in Method 130, Procedure 2, of the Technical Manual of the American Association of Textile Chemists and Colorists, Vol. 53, p. 253 (1978 ed.), and will be well-known to those skilled in the textile arts. While it will be appre-ciated that durability of bonding will depend upon such factors as the amount of TiO2 initially applied, method of application, substrate composition, and the presence on the material of binders and other additives, generally, the products of the present invention may be characterized in that at least about 50 percent, preferably about 70 percent or more by weight, of the titanium dioxide particles remain bound to the surface of the textile fibers after five standard AATCC washings. In certain preferred applications the durability of bonding may be even greater, e.g., about 80 percent or even greater after five AATCC
washings The textile material products of the present invention may be further characterized by certain additional advantageous properties in a textile product. For instance, the products generally exhibit improved "flat dry" characteristics as compared to known products where a binder is generally employed as the primary means of bonding the particles to the textile material.
The products of the present invention also exhibit improved moisture wicking properties as compared to known products. The soil release characteristics of the products of the present in-vention are also significantly improved by application of any of the known soil release agents as compared to known products of the same type where a binder has been employed since the proper-ties of most or all known binders in general are disadvantageous from a soil release standpoint.
Preferred embodiments of the process of the present in-vention will now be described in detail. In the context of the present invention, polyester fiber-containing textile materials that may be treated to provide a product having improved opacity may be a spun yarn, an extruded filament, a woven fabric, a knitted fabric, an unwoven web, or the like. Obviously, in the sense of strands such as spun yarns or extruded filaments, opacity will be apparent per se and will carry forward to a substrate formed therefrom, e.g., by weaving, knitting, non-woven techniques or the like. Extruded filaments per se or in fabric or web form may have a ro~md cross section, or preferably, may possess a non-round cross section such as multilobal, and are preferably texturized.
The terms "textured" and "texturized" are used herein interchangeably to refer to an otherwise smooth, continuous fila-mentary yarn which has been crimped, looped, coiled, or crinkled by any one of at least a dozen well-known techniques to impart mproved properties thereto, such as stretch, luxurious bulk, greater absorbency and/or improved hand. The most preferred texturized yarns of the invention are those made by false twist-ing of the yarn on any of the well-known and used false-twist .
type stretch yarn machines, such as those made by ARCT, Barmag, Berliner, Davide, Guidici and others. Among the many advantages of fabrics made from texturized yarns, particularly polyester yarns, are that they simulate some of the characteristics of fabrics made from spun yarns and provide certain additional ad-vantageous characteristics such as improved pill and crease resistance, better shape retention, great~r durability and more uniform appearance.
In the context of the present invention, the term poly-ester fiber means any polymeric ester that has been extruded into filamentary form. Conventionally, the polyester is the reaction . ~ i product of a dicarboxylic acid, or ester forming derivative of same and a glycol, e.g., dimethyl terephthalate and ethylene glycol that is condensed to provide a polymer of the glycol ester of the dicarboxylic acid. Such polyester may also contain other constituents to render the filaments extruded therefrom capable of basic dyeability, to impart antlstatic properties, flame re-tardant properties or the like.
In applying the titanium dioxide, which as indicated above should have an average particle size of at least about 0.18 micron, a good dispersion can be attained under alkaline conditions, which will remian stable for prolonged periods of time. As the pH of the dispersion is changed to the acid side, the titanium dioxide begins to exhaust therefrom. Gradual lowering of the pH of the dispersion achieves a quite uniform application of titanium dioxide onto the textile material. In fact, it was totally sur-prising to determine that relatively large amounts of titanium dioxide can be exhausted onto the textile material by the present techniques while retaining a good material handle for garment end use. Likewise, it was surprising to determine that the pigment is durable to repeated laundering and dry cleaning without the use of adhesive binders as the primary means for bonding the particles to the surface of the textile material.
When an initial dispersion has an acid pH, agitation is required to maintain proper dispersion stability, Likewise, uniformity of deposition of the titanium dioxide pigment appears less than when the initial dispersion has a basic pH, ~ . . . . .
While not wlshing to be bound by any particular theory, it is hypothecated that the titanium dioxide pigment begins to ex-haust from the dispersion at its isoelectric point where the electrical charge on the titanium dioxide particles changes from negative to positive. In any event, when the pH of the disper-sion becomes about 7.5 or below, exhaustion commences. A gradual reduction of pH of the dispersion permits the pigment to adhere to the textile material as it exhausts from the dispersion with little or no pigment precipitation from the bath. Too rapid a reduction of pH interferes with uniform application of pigment onto the substrate and tends to destroy stability of the dis-persion.
A proper dispersion of titanium dioxide pigment in water may be obtained by any suitable procedure. For example, for the preferred embodiment the pigment may be predispersed in a dilute alkaline solution, or may be added directly to the alkaline aqueous medium. Suitable alkaline materials include without limitation, ammonium hydroxide, sodium hydroxide and the like.
Thereafter, stirring will disperse the pigment in the medium as evidenced by a milky appearance, and the dispersion will remain stable. According to the present invention, the amount of titanium dioxide pigment in the dispersion may be in a range of from about 1.0 to about 20 weight percent based on the weight of textile material to be treated~ and preferably about 3 to about 7 percent. Up to 7 percent titanium dioxide based on material weight has been added to a textile material without "dusting" and with good durability to laundering and dry cleaning. In like vein, amounts of about 20 percent based on material weight have beed added with only slight "dusting."
During operation of the present proce~s, it is most de-sirable to maintain continuous relative movement between the dispersion and the textile material. Such may be accomplished by continuous agitation of the dispersion or movement of the textile material, or both. Since, as mentioned hereinafter, the present process is compatible with dyeing operations, the process may be conducted in commercial dyeing apparatus such as a jet rope dyeing apparatus where the textile material is handled in rope form, agitated by a jet of water or the like.
Once the substrate is in contact with the dispersion, the pH can then be lowered to promote the exhaustion. While any technique may be employed for lowering the pH of the dispersion, as mentionled above, the drop should be gradual. An acid, e.g., acetic acid, may be slowly added to the dispersion to lower the pH. At a pH above 4, it is preferable to heat the dispersion for complete exhaustion, while at a pH of 4 or below complete ex-haustion of the titanium dioxide will occur at ambient temperature.
A preferred technique, however, for adjustment of the dispersion pH is the addition of an acid generating compound which, when subjected to a predetermined condition, such as the application of heat, will liberate an acid which in turn lowers the pH of the dispersion. Butyrolactone, a compound marketed under the name SANDACID V by Sandoz Chemical Company is a preferred acid generating compound. Temperature increase is con-trolled to limit acid generation and, therefore, achieve thegradual pH reduction.
Though no ingredients are essential to operation of the present process other than those to disperse titanium dioxide in an aqueous medium and a means for adjusting pH of the dispersion, other ingredients may be included in the dispersion so long as they do not adversely affect exhaustion of the titanium dioxide, handle of the material for its intended use, durability of the treatment, or the like. Without limitation, such further ingred-ients which may or may not be present in sizable quantitiesinclude dyestuffs, dyestuff carriers, levelers, lubricants, chelating agents, optical brighteners, binders in a minor amount, and the like. In like fashion, after improving the opacity or cover of a textile material according to the process of the present invention, the textile material may thereafter be treated to impart crease resistant properties, soil resistant properties, fire retardant properties, and the like thereto. In fact, the present process may be conducted simultaneously with a soil re-lease or soil resistant treatment, though same is not preferred.
In general, whether the initial dispersion is alkaline or acid, exhaustion of the titanium dioxide occurs at a pH below about 7.5. As mentioned above, a preferred process utilizes an initially alkaline dispersion with the pH of same being gradually reduced to the acid side. Such produces a very uniform deposition of titanium dioxide on the substrate. Preferably, whether intially alkaline or acid, p~I of the dispersion during exhaustion falls in a range of from about 6 to about 3, with a most preferred range being from about 5 to about 4.
While the titanium dioxide applied to the polyester textile material is durable without other ingredients, subsequent appli-cations of crease resistant chemicals, soil resistant chemicals, or, as mentioned above a minor amount of an extraneous adhesive binder and the like, will add further durability. Likewise, the polyester textile material may be heat set after the titanium B~3 dioxide is added to further enhance durability. Heat setting, for example, will cause a substantially greater amount of titanium dioxide to be retained on the substrate after repeated washings and dry cleanings. Normally the heat settiny is con-ducted by subjecting the material to temperature in a range offrom about 300 to about 400F. for a residence time of from about 5 seconds to about 2 minutes. As mentioned above, while an ex-traneous adhesive binder is ordinarily not required to provide a product having good durability, a minor amount, e.g., about 2 percent or less by weight of an adhesive binder, may be applied to the material where desired.
The process according to teachings of the present in-vention may be better understood by reference to the following examples Example 1 A length of 100 percent texturized polyester fabric was placed in a Mathis laboratory dyeing apparatus, type JF. Water was then introduced into the dyeing apparatus at a temperature of 80F. adequate to provide a bath to fabric weight ratio of 30:1, and agitation started. Titanium dioxide pigment (TI-Pure 960 manufactured by DuPont) was predispersed in a dilute ammonium hydroxide solution in a Waring blender for five minutes. There-after, the titanium dioxide-ammonium hydroxide dispersion was added to the aqueous bath in the dyeing apparatus to an amount of pigment representing 5 percent of the weight of fabric, and pH of the bath was 9Ø After agitation for five further minutes, butyrolactone (SANDACID* V manufactured by Sandez Chemical Company) was added to the dispersion in an amount of 3 percent *Trademark X
~L~ 3 based on fabric weight. Temperature of ~he dlspersion was then raised at a rate of 3F. per minute to a temperature of 266F.
The 266F. temperature was held for five minutes after which the bath was cooled to 160F. Bath pH then measured 4.7, and ex-hibited clarity, indicating exhaustion of the pigment. Thefabric was then removed from the bath, rinsed once, dried and heat set at a temperature of 350F. for one minute. The processed fabric exhibited greatly improved opacity when compared to a con-trol fabric that was processed in like fashion without the presence of the titanium dioxide pigment. Weight an~lysis in-dicated that 95 percent of the titanium dioxide had exhausted from the dispersion onto the fabric. Improved opacity remained after repeated laundering and dry cleaning, evidencing durability, About-70 percent of the titanium dioxide particles remained after 5 AATCC washings.
Example 2 A length of 100 percent texturized polyester fabric was placed in a beaker of cold water with a water to fabric ratio of ` 30:1 and agitated. Ammonium hydroxide was then added to the bath adequate to bring the pH of the bath to 10Ø Titanium dioxide pigment was then added to the bath in an amount equivalent to 7 percent based on weight of the fabric (particle size 0.22 micron). Agitation was continued for five minutes after which pH of the bath was adjusted to 4.0 with the prolonged gradual addition of acetic acid. Temperature of the bath was then gradually raised to 212F. At a temperature of approximately 158F., appreciable exhaustion of the titanium dioxide pigment was noted. After fifteen minutes at 212F., the bath was clear 8~C)3 indicating almost complete exhaustlon of the titanium dioxide.
The fabric was removed from the bath, dried and cured at a temperature of 360F. for 30 seconds and weighed whereupon it was determinéd that 95 percent of the titanium dioxide pigment had exhausted onto the fabric. The fabric exhibited improved opacity which was durable to both laundering and dry cleaning.
Virtually no "dustinq" was noted, and a good fabric handle was apparent. About 70 percent of the titanium dioxide particles remained after 5 AATCC washings.
Example 3 _ The procedure of Example 2 was repeated with the excpetion that temperature of the bath was maintained at ambient conditions.
Again, virtually all the titanium dioxide exhausted onto the textile fabric, and improved, durable opacity resulted, though a longer period of time was required for complete exhaustion.
About 60 percent of the titanium dioxlde particles remained after 5 AATCC washings.
Example 4 Textured polyester fabric was processed as described in Example 1. The processed sample was then evaluated along with an untreated control to determine the initial opactiy of same and durability of opacity after repeated washing at 120F. for five minutes. Opacity was determined with a Hunter Color Difference Meter as discussed above. The value for ~ L indicates the degree of opacity ranging from 0 for total opacity to 100 for complete transparency. Results are set forth in Table I.
TABLE I
OPACITY OF TEXTURED POLYESTER FABRICS
Untreated I'iO
Control on Fahric, Heat Set Initial Opacity, ~ L 14.2 5.8 After 1 Wash, ~ L 14.0 6.7 After 5 Washes, ~ L 14.0 6.8 After 10 Washes, ~ L 13.9 7.0 After 20 Washes, ~ L 13.9 7.0 After 50 Washes, ~ L 13.9 7.3 Example 5 Fabric samples processed as set forth in Example 1, certain of which were not heat set, were subjected to up to 5 home laundering operations, during which titanium dioxide count was intermittently checked to further determine the durability of the titanium dioxide on the substrate. Results are indicated in Table II.
TABLE II
TiO2 Count Sample Initial After l Wash After 5 Washes Heat Set 684 542 420 Not Heat Set 765 282 177 Titanium dioxide count indicates the amount of titanium dioxide on the substrate and is a measure of intensity, corrected for background in counts per second determined by x-ray fluorescence. It is thus noted that durability is enhanced by heat setting, and with heat setting, appreciable amounts of titanium dioxide remain after repeated washings.
Example 6 Texturized 100 percent polyester was processed as described in Example 1 with the exception that the fabric was only dried and was not heat set. Thereafter, the fabric with the titanium dioxide thereon was padded with an emulsion containing a copoly-mer of methyl acrylate: acrylic acid (70:30) to provide 0.3 percent copolymer solids based on fabric weight. me fabric was then dried and heat set at 350F. for one minute. Good durable cover was found to be present for the fabric along with good soil release properties. About 70 percent of the titanium dioxide particles remained after 5 AATCC washings.
Example 7 Example 1 was repeated with the exception that a pink dispersed dyestuff was also incorporated into the bath to achieve 0.1 percent dyestuff based on fabric weight. The fabric ex-hibited improved opacity as with Example 1, and was dyed an even pink color. The fabric was subjected to repeated laundering and dry cleaning operations, and was durable both as to dye level and cover.
Example 8 As mentioned above, it is known that titanium salts may be used in dispersions that are applied to textile materials, such as cellulose acetate, rayon and the like to deluster same.
In such exhaustion techniques, which represent the closest prior .~ .
~ . . . . . .
8~ 3 art known to applicant at the time of filing of the application, the particle size of the titanium dioxide is generally 0.1 micron or smaller. Furthermore, the products of the present invention exhibit markedly improved physical characteristics as compared to products produced by such prior art exhaustion techniques, and Table III below illustrates the novel characteristics of the products of the present invention (see column 2) as compared to a control sample of the same fabric substrate to which no titanium dioxide particles have been applied (column 1). The same pro-cedure was follows to prepare the sample illustrated in column2 that is set forth in Example 1 except that the pigment used was Titanox 1070, an anatase product manufactured by NL Industries.
A sample of the same fabric treated by a known exhaustion tech-nique, namely Example 1 of U. S. Patent No. 2,309,294 (herein the '294 patent), wherein the titanium dioxide particles of the same type used to prepare the sample of column 2 were exhausted from a bath containing aluminum formate is illustrated in column 3. Column 4 shows the physical characteristics of the same substrate treated by padding according to the process of Example 2 of the '294 patent. Column 5 provides the physical characteristics of the same substrate processed again according to Example 1 except that the bath contalned aluminum sulfate rather than aluminum ~ormate. In the Table the designation P
stands for poor, F-G stands for fair to good, G stands for good, VG stands for very good, and E stands for excellent.
~B~3 TABLE I I I
Without Soil Release Finish Product Aluminum 294 2 Aluminum Characteristics Control Invent~on Formate Padded Sulfate -Cover P E P F~G F
5 Durability of Cover - G P P P
Hand G G G P F-G
Moisture Transport P E P P P
Crocking - VG VG P P
Agglomeration - Slight Medium ~eavy Medium 10 Soil Hiding P G P F-G F
% Exhaustion - 80 20 - 50 Example 9 In this Example the same samples used in Example 8 and Table III were all padded according to the procedure set forth in Example 6 with a soil release emulsion containing a copolymer of methyl acrylate: acrylic acid (7Q:30), an ethoxylated poly-ester and a lubricant (ethoxylated oleic acid) to provide 0~3 percent copolymer solids, 0.15 percent ethoxylated polyester and 1.0 percent lubricant based on the fabric weight. The re-~0 sulting properties of the textile materials are set forth belowin Table IV:
X
. .
TABLE IV
With Soil Release E~inish Aluminum 294 2 Aluminum Control "CUMULUS" Format'e Padded Sulfate Cover P E P F F
5 Durability of Cover - G P P P
Hand G G G P F
Soil Release G G G G G
Moisture Transport G E G G G
Crocking - VG VG P P
10 Agglomeration - SlightMedium Heavy Medium Soil Hiding P G P F-¢ F
~ Example 10 : Example 1 was repeated on a length of 100 percent spun polyester woven fabric instead of texturized polyester. The processed fabric exhibited greatly improved opacity ( ~ L value of 9.1) when compared to a control fabric that was processed in like fashion without the presence of the titanium dioxide pigment ( ~ L value of 18.3). Improved opacity remained after repeated launderings ( ~ L value of 13.0 after 5 washings as compared to ~ L value of 18.2 for the control fabric).
Example 11 Example 1 was repeated again on a length of 100 percent filament (untexturized) polyester woven fabric instead of the texturized polyester of Example 1. The processed fabric exhibited ~.
.
.
greatly improved opacity ( ~ L value of 17.0) when compared to a control fabric that was processed in like fashion without the presence of titanium dioxide pigment ( ~ L value of 28.5).
~ Example 12 Example l was repeated once more on a length of nylon taffeta fabric instead of the lO0 percent texturized polyester fabric of Example l. While the processed fabric exhibited some improved opacity initially ( ~ L value of ll.9) as compared to a control fabric that was processed in like fashion without the presence of titanium dloxide pigment ( ~ L value of 24.5) after only 5 standard washings only about 8.7 percent of the particles initially present on the fabric remained.
Example l3 Example l was repeated on a length of lO0 percent woven acrylic fabric instead of the texturized polyester of Example l.
While the processed fabric exhibited some improved opacity initially ( ~ L value of 3.2) as compared to the control fabric that was processed in a like fashion without the presence of titanium dioxide pigment ( ~ L value of 15.0) af-ter only 5 standard washings only about 25 percent of the particles initially present on the fabric remained.
Example 14 Example l was repeated on a length of 65/35 polyester/
cotton blend woven fabric instead of the lO0 percent texturized polyester of Example l. While the processed fabric exhibited some improved opacity initially ( ~ L value of 6.2) as compared to a control sample that was processed in a like fashion without ~ .
the presence of titanium di.oxide pigment ( ~ L value of 16.0) after only 5 standard washings only about 24 percent remained on the fabric. The ~ L value after 5 washings of the treated sample was 10.2, however, which compared favorably even against the ini.tial opacity of the control sample.
X
.
Claims (37)
1. A polyester fiber-containing textile material having improved opacity and handle characteristics, which comprises a polyester fiber-containing substrate; said textile fibers having been covered with titanium dioxide particles having an avergae particle size of at least about 0.18 micron in an amount of up to about 20 percent based upon the weight of the textile material, the durability of bonding of said particles to said textile fibers in the absence of a binder as the primary bonding means being such that at least about 50 percent of said particles remain bound to the surface of said textile fibers after five standard AATCC washings.
2. A polyester fiber-containing textile material having improved opacity and handle characteristics, which comprises a polyester fiber-containing substrate; said textile fibers having been covered with titanium dioxide particles having an average particle size of at least about 0.18 micron in an amount of up to about 20 percent based upon the weight of the textile material, without substantial agglomeration of said particles between said textile fibers, the durability of bonding of said particles to said textile fibers in the absence of a binder as the primary bonding means being such that at least about 50 percent of said particles remain bound to the surface of said textile fibers after five standard AATCC washings.
3. The polyester fiber-containing textile material of Claims 1 or 2 wherein said textile material is a woven fabric form.
4. The polyester fiber-containing textile material of Claims 1 or 2 wherein said textile material is a knitted fabric.
5. The polyester fiber-containing textile material of Claims 1 or 2 wherein said textile material contains at least about 10 percent by weight polyester fibers.
6. The polyester fiber-containing textile material of Claim 5 wherein said textile material is all polyester.
7. The polyester fiber-containing textile material of Claims 1 or 2 wherein said titanium dioxide particles are present in an amount of up to about 7 percent by weight.
8. The polyester fiber-containing textile material of Claims 1 or 2 wherein said titanium dioxide particles are ad-hered to the surface of said textile fibers in the absence of an adhesive binder.
9. The polyester fiber-containing textile material of Claims 1 or 2 wherein a minor amount of binder is applied to the textile material as a secondary bonding means to further improve the durability of bonding said material.
10. The polyester fiber-containing textile material of Claim 9 wherein said binder is present in an amount of less than about 2 percent by weight.
11. The polyester fiber-containing textile material of Claims 1 or 2 wherein said polyester fibers are extruded texturized filaments.
12. The polyester fiber-containing textile material of Claims 1 or 2 wherein said titanium dioxide particles cover the surface of said polyester fibers in a manner such that the average agglomerate size is less than about 50 primary particles per agglomerate.
13. The polyester fiber-containing textile material of Claims 1 or 2 wherein the durability of bonding of said particles to said textile fibers is such that at least about 70 percent of said particles remain bound to the surface of said textile fibers after 5 standard AATCC washings.
14. A process for improving opacity of a polyester fiber-containing textile material comprising the steps of:
a) providing an aqueous dispersion of titanium dioxide pigment having a particle size of at least about 0.18 micron;
b) contacting said textile material with said aqueous dispersion under agitation conditions and at a pH of less than about 7.5 whereby said titanium dioxide pigment exhausts from said dispersion; and c) thereafter heat setting said material.
a) providing an aqueous dispersion of titanium dioxide pigment having a particle size of at least about 0.18 micron;
b) contacting said textile material with said aqueous dispersion under agitation conditions and at a pH of less than about 7.5 whereby said titanium dioxide pigment exhausts from said dispersion; and c) thereafter heat setting said material.
15. The process as defined in Claim 14 wherein said dis-persion pH during at least a portion of the time of contact with said material is in a range of from about 6 to about 3.
16, The process as defined in Claim 14 wherein said dis-persion pH during at least a portion of the time of contact with said material is in a range of from about 5 to about 4.
17. The process as defined in Claim 14 wherein said dis-persion is initially alkaline and pH is gradually reduced to a point below about 7.5.
18. The process as defined in Claim 17 wherein said pH
is reduced by including an acid generating compound in the dis-persion and heating the dispersion for the generation of acid.
is reduced by including an acid generating compound in the dis-persion and heating the dispersion for the generation of acid.
19. The process as defined in Claim 17 where pH of the dispersion is reduced by the gradual addition of acid thereto.
20. A process for improving opacity of a polyester fiber-containing textile material comprising the steps of:
a) providing an aqueous dispersion of titanium dioxide pigment having a particle size of at least about 0.18 micron, said dispersion having a pH above about 7.5;
b) contacting said textile material with said aqueous dispersion under agitation conditions; and c) gradually reducing pH of the dispersion to a level below approximately 7.5 whereby said pigment exhausts from said dispersion onto said textile material.
a) providing an aqueous dispersion of titanium dioxide pigment having a particle size of at least about 0.18 micron, said dispersion having a pH above about 7.5;
b) contacting said textile material with said aqueous dispersion under agitation conditions; and c) gradually reducing pH of the dispersion to a level below approximately 7.5 whereby said pigment exhausts from said dispersion onto said textile material.
21. The process as defined in Claim 20 wherein the process is carried out at ambient temperature and the pH is reduced by the gradual addition of an acid.
22. The process as defined in Claim 20 wherein the dis-persion further contains a heat activated acid generating compound, and the dispersion is gradually heated to generate acid and lower pH of the dispersion for exhaustion of the titanium dioxide pigment.
23. The process as defined in Claim 20 wherein the initial pH of the dispersion is approximately 9, and the pH of the dispersion is gradually reduced to a pH in the range of from about 6 to about 3.
24. The process as defined in Claim 23 wherein the dis-persion contains butyrolactone, and the dispersion is heated to a temperature of about 266°F., whereby acid is generated which gradually lowers the pH of the dispersion to about 4.7.
25. The process as defined in Claim 20 comprising further heat setting the polyester textile material.
26. The process as defined in Claim 25 wherein the textile material is heat set at a temperature in a range of from about 300°F. to about 400°F. for from about 5 seconds to about 2 minutes.
27. A process for improving opacity of a polyester fiber-containing textile material comprising the steps of:
a) providing a binderless, aqueous dispersion com-prising titanium dioxide pigment at a pH above approximately 7.5, said pigment having an average particle size of at least about 0.18 micron, and an acid generating substance;
b) contacting said textile material with said dis-persion and creating relative movement therebetween;
c) gradually heating said dispersion with said textile material therein up to a temperature of approximately 266°F., at which point acid will have been generated adequate to lower pH
of the dispersion within the range of about 6 to about 3, whereby substantially all the titanium dioxide pigment will exhaust onto the textile material; and d) heat setting the textile material.
a) providing a binderless, aqueous dispersion com-prising titanium dioxide pigment at a pH above approximately 7.5, said pigment having an average particle size of at least about 0.18 micron, and an acid generating substance;
b) contacting said textile material with said dis-persion and creating relative movement therebetween;
c) gradually heating said dispersion with said textile material therein up to a temperature of approximately 266°F., at which point acid will have been generated adequate to lower pH
of the dispersion within the range of about 6 to about 3, whereby substantially all the titanium dioxide pigment will exhaust onto the textile material; and d) heat setting the textile material.
28, The process as defined in Claim 27 wherein the acid generating substance is butyrolactone and the pH of the dispersion is lowered to about 4.7.
29. The process as defined in Claim 27 wherein heat setting of the textile material is conducted at a temperature in the range of from about 300°F. to about 400°F. for a time period of from about 5 seconds to about 2 minutes.
30. A polyester fiber-containing textile material having improved opacity and handle characteristics which comprises a polyester fiber-containing substrate; said textile fibers having been covered with titanium dioxide particles having an average particle size of at least about 0.18 micron in an amount of up to about 20 percent based upon the weight of the textile material, the durability of bonding of said particles to said textile fibers in the absence of a binder as the primary bonding means being such that at least about 50 percent of said particles remain bound to the surface of said textile fibers after 5 standard AATCC washings, wherein a minor amount of binder is applied to the textile material as a secondary bonding means to improve durability of bonding of said particles; and wherein said titanium dioxide particles cover the surface of said polyester fibers in a manner such that the average agglomerate size is less than about 50 primary particles per agglomerate.
31. The polyester fiber-containing textile material of Claim 30 wherein said textile material is a woven fabric form.
32. The polyester fiber-containing textile material of Claim 30 wherein said textile material is a knitted fabric.
33. The polyester fiber-containing textile material of Claim 30 wherein said textile material contains at least about 10 percent by weight polyester fibers.
34. The polyester fiber-containing textile material of Claim 30 wherein said textile material is all polyester.
35. The polyester fiber-containing textile material of Claim 30 wherein said titanium dioxide particles are present in an amount of up to about 7 percent by weight.
36. The polyester fiber-containing textile material of Claim 30 wherein said polyester fibers are extruded texturized filaments.
37. The polyester fiber-containing textile material of Claim 30 wherein the durability of bonding of said particles to said textile fibers is such that at least about 70 percent of said particles remain bound to the surface of said textile fibers after 5 standard AATCC washings.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
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US4003279A | 1979-05-17 | 1979-05-17 | |
US40,032 | 1979-05-17 | ||
US7295979A | 1979-09-06 | 1979-09-06 | |
US72,959 | 1979-09-06 | ||
US06/128,619 US4283452A (en) | 1979-09-06 | 1980-03-10 | Polyester textile material having improved opacity |
US128,619 | 1980-03-10 |
Publications (1)
Publication Number | Publication Date |
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CA1148803A true CA1148803A (en) | 1983-06-28 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000352026A Expired CA1148803A (en) | 1979-05-17 | 1980-05-15 | Polyester textile material having improved opacity |
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AU (1) | AU5847880A (en) |
CA (1) | CA1148803A (en) |
DE (1) | DE3018836A1 (en) |
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ES (2) | ES8105809A1 (en) |
FR (1) | FR2457335A1 (en) |
GB (1) | GB2051163B (en) |
IT (1) | IT8048711A0 (en) |
LU (1) | LU82449A1 (en) |
NL (1) | NL8002847A (en) |
PT (1) | PT71246A (en) |
SE (1) | SE8003627L (en) |
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US4459445A (en) * | 1981-03-02 | 1984-07-10 | Mitsubishi Denki Kabushiki Kaisha | Circuit breaker |
CN113227485A (en) * | 2018-12-28 | 2021-08-06 | 尚科纺织企业工业及贸易公司 | Method for producing a textile product and textile product obtained thereby |
CH716250A2 (en) * | 2019-06-04 | 2020-12-15 | Schoeller Tech Ag | Opaque textiles for clothing. |
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1980
- 1980-05-14 LU LU82449A patent/LU82449A1/en unknown
- 1980-05-14 SE SE8003627A patent/SE8003627L/en not_active Application Discontinuation
- 1980-05-15 GB GB8016127A patent/GB2051163B/en not_active Expired
- 1980-05-15 CA CA000352026A patent/CA1148803A/en not_active Expired
- 1980-05-15 PT PT71246A patent/PT71246A/en unknown
- 1980-05-16 IT IT8048711A patent/IT8048711A0/en unknown
- 1980-05-16 NL NL8002847A patent/NL8002847A/en not_active Application Discontinuation
- 1980-05-16 DK DK216480A patent/DK216480A/en unknown
- 1980-05-16 DE DE19803018836 patent/DE3018836A1/en not_active Withdrawn
- 1980-05-16 AU AU58478/80A patent/AU5847880A/en not_active Abandoned
- 1980-05-16 ES ES491551A patent/ES8105809A1/en not_active Expired
- 1980-05-16 FR FR8011033A patent/FR2457335A1/en not_active Withdrawn
- 1980-08-25 ES ES494484A patent/ES494484A0/en active Granted
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IT8048711A0 (en) | 1980-05-16 |
GB2051163A (en) | 1981-01-14 |
DK216480A (en) | 1980-11-18 |
SE8003627L (en) | 1980-11-18 |
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ES8106572A1 (en) | 1981-07-01 |
NL8002847A (en) | 1980-11-19 |
ES491551A0 (en) | 1981-06-01 |
LU82449A1 (en) | 1980-12-16 |
DE3018836A1 (en) | 1980-11-20 |
ES8105809A1 (en) | 1981-06-01 |
FR2457335A1 (en) | 1980-12-19 |
GB2051163B (en) | 1982-12-15 |
ES494484A0 (en) | 1981-07-01 |
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