|Publication number||US3849159 A|
|Publication date||Nov 19, 1974|
|Filing date||Aug 6, 1973|
|Priority date||Aug 6, 1973|
|Also published as||CA1035908A, CA1035908A1|
|Publication number||US 3849159 A, US 3849159A, US-A-3849159, US3849159 A, US3849159A|
|Inventors||L Palmer, R Conger|
|Original Assignee||Congoleum Ind Inc|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (8), Referenced by (38), Classifications (13), Legal Events (7)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent ,
Palmer et al.
[451 Nov. 19, 1974 1 CARPET EMBOSSING IN REGISTER WITH PRINT  Inventors: Leon B. Palmer, Little Falls; Robert P. Conger, Park Ridge, both of NJ.
 Assignee: Congoleum Industries, Inc., Kearny,
22 Filed: Aug. 6, 1973 21 App1.No.:386,048
 US. Cl 117/11, 26/69 B, 28/76 P, 156/277, 161/63  Int. Cl. B44d l/02, B44d 5/02, D03d 27/00  Field of Search 161/63; 156/277; 117/8.5, 117/9, 11; 26/69 B; 28/76 P  References Cited UNITED STATES PATENTS 556,794 3/1896 Wissel et al. 26/69 B 1,223,018 4/1917 Zeidler 26/69 B UNTREATED FIBER$7 BACKING 1,655,414 1/1928 Flory 26/69 B 1,834,339 12/1931 Dreyfus et a1.. 26/69 B 2,020,698 ll/1935 Platt 161/63 2,875,504 3/1959 White t 161/63 2,901,373 8/1959 Weiss 117/11 3,567,548 3/1971 Miller 156/277 Primary Examiner-William J. Van Balen Attorney, Agent, or FirmRichard T. Laughlin [5 7] ABSTRACT Pile fabrics prepared from nylon carpet fibers having a textured or embossed surface and aprocess of developing the textured effect which comprises se1ectively contacting the surface of said carpet with a chemical fiber shrinking agent therefor, allowing the shrinking action to occur and, thereafter, effectively removing the shrinking agent from the surface, said shrinking serving to reduce the height of the pile in the treated areas and creating said textured surface.
19 Claims, 2 Drawing Figures FIBERS TREATED WITH EMBOSSING AGENT fi t v r UNTREATED FIBERS PATENTL 33v 1 91974 FIG] EMBOSSED AREA UNTREATED AREA FIBERS TREATED WITH UNTREATED FIBERS EMBOSSING AGENT UNTREATED FIBERS BACKING CARIET EMBOSSING IN REGISTER WITH PRINT BACKGROUND OF THE INVENTION In the production of nylon pile fabrics, it is often desirable to emboss the surface thereof in order to provide added decorative appeal. In some instances, the embossed areas are printed with dyes to further embellish the surface design.
Embossing of pile fabrics is conventionally accomplished with a heating embossing roll or place which has been engraved or otherwise treated to create the design desired in raised relief on the surface. A method which eliminates the use of embossing rolls has been disclosed in US. Pat. Nos. 2,790,255 and 2,875,504. In accordance with these patents, the pile fabric is formed from a combination of shrinkable and non-shrinkable yarns. Upon subjecting the fabric to the influence of heat, the pile formed from the shrinkable yarns contracts while the base and the nonshrinkable yarns remains intact thereby yielding a pile made up of high and low areas to give the appearance of an embossed or carved product.
A chemical embossing method is disclosed in US. Pat. No. 2,020,698. According to this patent, fabric having a pile of organic ester of cellulose yarn is locally treated with an alkali or alkaline salt saponifying agent in order to obtain ornamental differential effects in the treated areas. Furthermore, since the organic ester of cellulose pile yarns that have not been saponified are more difficult to change from their position, after they are once set than are the saponified organic ester of cellulose yarns, it is possible to obtain a differential lay between the saponified and unsaponified organic ester of cellulose pile yarn. Thus, the fabric, after the application of the saponifying agent, may be washed, finished and dried with the pile erect, after which the fabric may be run through water and brushed across the piece to lay the pile towards the selvage and it is then dried, This causes the saponified pile yarn to lie flat while the unsaponified yarn remains substantially erect. Upon subsequent steaming and brushing the fabric in the opposite direction, any unsaponified yarn which may have been slightly bent from the vertical by the previous brushing toward the selvage is caused to stand erect without disturbing the position of the laid or crushed saponified organic ester of cellulose pile yarn.
SUMMARY OF THE INVENTION It is the primary object of this invention to provide a simple process for producing a nylon pile having a textured or embossed surface.
Another object is to provide such a process which is readily adaptable to standard printing equipment.
Another object is to provide a process which allows the production of pile fabric having embossed areas in register with a printed design.
A further object is to provide an embossing process which is readily adaptable to curved and irregular surfaces.
Various other objects and advantages of this invention will be apparent from the following detailed description thereof.
It has now been discovered that it is possible to produce superior nylon fabrics having embossed surfaces by contacting selected portions of the surfaces with a chemical embossing agent for the fibers of said pile fabric causing dimensional change by linear contraction of the treated fibers and, thereafter, effectively removing the embossing agent. The resulting product is thus depressed at the treated areas.
The embossing composition can be transparent so that the appearance of the product is not altered other than in being embossed. Alternatively, the embossing agent can be part of a dye or pigment composition used in printing the fabric so that the color appears in perfect register in the areas of embossing agent application.
The depth of the depressed areas can be controlled by varying the concentration and/or type of embossing agent. This variation in concentration can be effected by the amount of vehicle applied as well as by the strength of 'the embossing reagent.
Furthermore, the embossed depth can be controlled to some degree by the depth of penetration of the print paste carrying the embossing agent as well as the steamer time and steamer temperatures to which the pile fabric is subjected in order to activate the chemical embossing agent which provide the desired effect.
This discovery makes possible the production of a product having embossed surfaces which can be in complete register with a printed design. Additionally, the discovery makes possible the utilization of many types of printing apparatus for purposes of effecting embossing, thereby eliminating the need for expensive embossing equipment. Further, it allows the embossing of a surface without exerting sufficient pressure to permanently deform the pile fabric. A great number of products can be produced by the process. They can be used for floor, wall and ceiling coverings, drapery,-upholstery and the like, and, in fact, wherever pile fabrics are utilized. They are readily adaptable to decorating any surface on which pile fabrics can be applied. Many additional applications will occur to those skilled in the art.
This invention will be better understood from the following detailed description thereof together with the accompanying self-explanatory drawings in which:
FIG. 1 is enlarged top view of a section of an embossed product of this invention; and,
FIG. 2 is an enlarged cross-sectional view of the same product taken through line 2-2.
DESCRIPTION OF THE PREFERRED EMBODIMENTS In the production of the pile fabrics of this invention, the pile yarn employed is nylon. Synthetic fibers prepared from polyamides such as nylon are well known to those skilled in the art.
Likewise, the embossing agents which are applied to the nylon fibers in order to produce the desired effect are also known chemical compounds. For purposes of this invention, the term embossing agent is defined as any active chemical composition which when applied to the pile fabric produces a measurable reduction of pile height, but without significant deterioration of the nylon fibers. In fact, it is our objective to induce embossment and shrinkage without deteriorating the fiber. The exact chemical and physical mechanism by which this result is achieved is not completely understood. However, it is believed that the embossing agent may owe its effectiveness largely to its capability. to function as a hydrogen bond breaker. Initially, the fibers are in a stretched and crystalline state. When the hydrogen bond is broken between the polymer chains, the fibers relax and shrink. Regardless of the mechanism, the overall effect produced is one of dimensional change, the most desirable effect, involving linear contraction of the fiber.
In order to be applicable for the novel process of this invention, the embossing agent should provide a reduction of the pile height through a shrinkage reaction, should not adversely affect the printing means, e.g., print screens, and should be capable of being substantially removed or inactivated subsequent to the embossing action. Other characteristics of the embossing agent which are desirable, though not essential, include compatibility with dye print pastes, capability of being regulated by factors of time, temperature, and concentration, i.e., susceptibility to activation by a conventional steaming operation and exhibiting no residual embossing activity. Needless to say, minor adjustments in the nature of the components and process conditions, and/or the embossing apparatus can be employed to overcome the absence of certain of these desired characteristics.
The embossing agent for the nylon fibers is applied to one surface of the pile fabric in any desired design, whether it be random or predetermined. One of the easiest methods of applying the agent is by utilizing conventional printing technique such as silk screen or block printing. The embossing agent can be applied as a concentrate, as part of a transparent vehicle, or as part of a dye composition utilized for pile fabric printing. The nature of the embossing agent dictates the nature of the vehicle to be utilized. Among such applicable vehicles are included: water, and alcohols such as methanol and isopropanol. Often thickeners, e.g., gums, and cellulose derivatives, are included in order to obtain viscosity characteristics demanded in print technology and to enable the embossing agent to adhere to and operate on the synthetic fiber and to hold the printed pattern.
In those instances where it is desired to acheive a singleor multi-colored printed decoration with a distinct color for the embossed areas, the embossing agent can be incorporated into a particular dye or pigment composition. The dye or pigment will generally be in the form of a print paste ink to which the appropriate amount of agent is added. It is to be noted that in preparing these modified dye composition, the pH levels, viscosities, and dye concentrations which are essential to an efficient dyeing operation must also be controlled. The resultant cffect is an embossed design in register with the printed pattern. If different depths of embossing are sought, they are achieved by use of different concentrations of agent in the areas calling for such different depths.
Generally, it is desirable that the embossing agent be soluble or in solution in the solvent medium from which it is applied to the selected areas of the fabric. However, if the agent is not soluble it should be in the composition in a form at least sufficiently finely divided to pass through the print screen, that is, it should be present in a micro pulverized form which indicates particle diameter of the order of I microns or smaller. That is, it must not only pass through a screen but it must pass through freely, dispersed through the dye paste throughout the printing operation. The purpose of this, of course, is to make sure that the agent becomes uniformly dispersed over the fiber in the print process so that the shrinking effect will be uniformly developed in the fiber.
As previously indicated, the preferred embossing agent is one which is dormant during the successive printing operations but then is activated by the elevated temperature of a steam chamber usually utilized to fix the dye onto the fibers. Embossing agents which can function in this manner on nylon and produce shrinkage ofthe nylon fibers comprise thiourea and its derivatives preferrably certain ofits more water soluble lower 1,3 dialkyl derivatives having the structure.
R i s NH wherein R, R and R" equals any combinations of H, N-acetyl, methyl, ethyl, propyl, butyl, isopropyl, pentyl, hexyl, and the like in comination with relatively low concentration of acids, such as formic, acetic, phosphoric, oxalic, and hydrochloric. Acids, such as monochloroacetic acid, are excluded if they react with thiourea or its derivatives by undergoing a substitution reaction with the mercaptide ion. At the individual concentrations employed in this process, thiourea or its derivatives alone, or the acid alone, are not useful. The advantages of this type of chemical embossing agent are that there is no need for rigid time control in the process and there is minimal concern regarding excessive uncontrollable embossing because other factors can be changed. Thus, the degree of diminution of the pile height can be controlled by adjusting the amount of dye paste applied, the concentration of embossing agent in the dye paste and the temperature and time of exposure in the steam chamber. All these factors can be adjusted according to properties of the nylon fiber comprising the pile fabric. While the depth of embossing will be determined by the practitioner in accordance with the type of embossed product being prepared, reduction in pile height will generally not exceed more than about 50 percent, this value being indicative of excellent embossing without exposing the backing materials.
Embossing can be achieved, if desired, by subjecting the treated fibers to heat. Thus, the treated surfaces may be subjected to the radiation from a bank of infrared lamps, particularly where the embossing agent is not part of a dye print paste. Additionally, even where the steaming operation is not essential to activate the embossing agent, such steaming may have the effect of increasing the penetration of the embossing agent and increasing the speed of its action on the fibers.
A critical step of the novel process of this invention involves terminating the embossing action and/or effecting substantial removal of the embossing agent from the pile fabric. It may be necessary to achieve complete elimination of all residues of the embossing process which may contribute undesirable properties to the finished fabric, such as odor, toxicity and color and texture change. Needless to say, any termination or quenching technique resorted to will depend on the particular embossing composition employed. The most useful technique for removing residues of the embossing process is by thoroughly washing the fabric with water and detergents. ln those instances where the embossing agent is part of a dye or pigment composition, the washing cycle which is utilized to remove excess dye or pigment serves also to removed traces of the agent. Where an acidic embossing agent is utilized, e.g., formic acid on nylon, it is possible to halt the embossing action more rapidly by rinsing with an aqueous ammonia or mildly alkaline solution. This neutralization of the acid serves to insure the total removal thereof.
Other techniques for terminating the embossing action and/or removing the embossing agent include evaporation and dry cleaning. Thus, if the agent is volatile, steaming of the treated pile fabric will serve to evaporate a large portion of the embossing pile content. Where rinsing techniques are not effective, it may be necessary to resort to a dry cleaning procedure to remove the embossing residues.
The invention has particular application to tufted carpets which are to have a printed decoration applied thereon. Unusual design effects can also be obtained when the pile fabric is printed with a multi-colored design wherein one or more of the dye compositions contain the appropriate embossing agent. The process of printing such carpets includes the steps of passing carpets, tufted of unpigmented or colored fibers, into a screen printing apparatus whereby a design is printed on the surface of the carpet. Each screen applies a separate color to make up the final design. The embossing agent can be added to one or more of these printing stations by addition to the dye composition, or it can be applied by a separate station in a transparent vehicle. The fabric is then passed into a steaming chamber to set the dyes and cause embossing and then to a washing cycle which serves to remove excess dye as well as to terminate the embossing action and/or remove the embossing components.
Accordingly, in the embossing of carpet or textured pile fabric, and for all practical purposes we are discussing the embossing of carpeting, it is important that any color design on the surface of the carpet which is related to the embossing be in accurate register with the embossing. Since we are concerned only with chemical embossing the problem is then one of inducing the differential fiber length between the embossed colored areas and unembossed areas and, while it is possible to induce shrinkage of synthetic nylon fibers, it is necessary for preparation of the carpet that the fiber shrinkage be induced with no significant deterioration of what is left. Thus, if the operation of embossing involves true shrinkage the shrunk fabric fiber should have a texture approximating that of the original.
In order to practically evaluate the utility of a particular chemical or combination of chemicals as an embossing agent for nylon carpet, the chemical system is incorporated in the dye printing paste and applied to a section of the nylon carpet by means of a screen printing technique so as to simulate plant production procedure as closely as possible. The treated carpet sample is steamed for minutes at 2l5-220F. (102C. 104C), thoroughly rinsed with water and dried at l80F. The depth of embossment is then measured and observations made regarding the character of the embossed nylon. e.g., strength, brittleness, softness, definition, color. Measurement of the pile height at the embossed and unembossed areas is made by means of a thin, steel ruler marked off in 1/64 inch (0.4 millime ter) intervals. Any method of measurement is useful so long as it is standardized from operation to operation and is reproducible to about 1/64 inch.
However, for the preliminary determination of whether or not a chemical composition is capable of shrinking nylon fibers and for thus determining its potential suitability as a chemical embossing agent for nylon carpet, we have devised a simpler, less time consuming beaker test procedure. Using this test, the per cent shrinkage and the per cent weight loss experienced by a centimeter loop of nylon carpet filament or carpet yarn is determined by immersing the yarn loop in an aqueous solution or dispersion of the test chemical for IS minutes at 2l5F (102C). This test affords a simple way of determining if a selected chemical will cause a shrinkage of the nylon fibers and provides a means of predicting whether or not a chemical will function as an embossing agent for nylon carpet. Also, the test provides a method for determining such effects as chemical concentration, temperature, time, print paste additives, solvents other than water, nylon type and construction and the like. Details of the test procedure are outlined as follows in Table I.
TABLE I BEAKER TEST PROCEDURE 1. Prepare a solution or dispersion of the chemicals to be tested in Water.* If heated, cool to room temperature. Weigh 30 grams into a 32 X 200 mm test tube.
2. Place test tube in preheated Silicone bath and heat contents of test tube to the desired temperature (usually 2l5F 102C).
3. Cut approximately 1 meter length of nylon yarn or filament and tie in a single loop.
4. Hang the loop under 50 gram load for 30 seconds and measure the length of the loop to 0.1 cm.
5. Weigh loop to nearest l/lO mg.
6. Immerse nylon loop in hot chemical solution, agitate gently and observe any change in character of the nylon fibers. Generally hold for 15 minutes or less.
7. Remove the nylon loop and wash thoroughly in copious amounts of water. Blot and dry to constant weight at room conditions.
8. Measure length'of nylon loop as in 4.**
9. Determine weight of nylon loop as in 5.
l0. Calculate percent shrinkage and percent weight loss.
* Dye print paste may be used if desired. Other solvents may be used. especially when other solvent based printing systems are employed. lf loop breaks or is already fragmented or disintegrated, or if insignificant shrinkage is obtained, repeat at lower or higher chemical eoncentratlon.
With the information thus obtained concerning the extent of shrinkage of the nylon fibers as well as any deterioration of the nylon fibers, it then becomes possible to determine whether or not the chemical composition has any potential as an embossing agent, and eventually proceed to the formulation of a printing paste which includes the shrinking material. Experience has shown, however, that while such test results prove that the chemical agent will shrink nylon fiber and thus has an embossing capability for nylon carpet, these results tell us only approximately what concentration of the chemical agent is required to emboss nylon carpet. Nor do we know the exact extent of the fiber deterioration that will be experienced on the nylon carpet. Generally, the following relationship seems to exist between beaker test results and screen printing test results on nylon carpet. Beaker test shrinkage results must reach at least without causing unacceptable nylon carpet fiber deterioration is usually about 50 percent.
Apparently, the difference between beaker test shrinkage results obtained on a loop of nylon filament urea and 15 percent formic acid (90 percent) causes the nylong loop to shrink 47.5 percent accompanied by about 10 percent weight loss in the shrunk nylon fibers without deterioration of the fiber properties (Run No. 47). Lower concentrations of formic acid yield less shrinkage, while at 20 percent formic acid (90 percent) nylon fiber is critically deteriorated becoming very fragile (Run No. 53). Thiourea alone at 50 percent yields a much lesser shrinkage of only about 15 percent and formic acid (90 percent) alone at 15 percent yields a shrinkage of only about 9.0 percent. comparable to water alone at 10.0 percent. With thiourea at a concentration of 50 percent the nylon filament shrinkage and weight loss increased significantly as the amount of formic acid is increased from to 20 percent. Hence, it
of yarn, and screen printing test results obtained on 15 tht the thiourea formic acid combinations is nylon carpet, occurs because the chemical is utilized i We in develo in n on shrinka e much less effectively on the carpet pile than in the beav. 8 9. a, .P y g TABLE II N lon Filament Shrink- Weight age Loss Loop Run No. Chemicals Character 15,17,30,35 avg. Water 10.0 1.50 Good 32 Thiourea, 50% 15.1 0.93 Good 26 90% Formic Acid, 5% 7.4 0.27 Good 46 90% Formic Acid, 10.7 1.30 Good 49 90% Formic Acid, 9.4 1.41 Good 54 90% Formic Acid, 8.5 1.62 Good 33 Thiourea, 5070/9070 Formic 21.3 1.77 Good Acid. 5% 44 Thiourea, 50%/90% Formic 38.5 4.53 Good Acid, 10% 47 Thiourea, 50%/90% Formic 47.5 10.0 Good Acid, 15% 53 Thiourea, 50%/90Z' Formic 72.3 41.0 Fragile Acid. 20%
ker test. Screen printing does not supply sufficient print While formic acid is the preferred a Other acids paste (containing embossing agent) to the nylon carpet may be used with thiourea with results as tabulated in pile to provide a completely uniform coating of the Table 111. nylon fibers. Furthermore, the depth of concentration One of the practical requirements of the shrinking into the carpet pile is often of the order of only about g n i h it rem in in l i n t room emperature 50 percent. Also, during steaming, the concentration of the embossing agent may be reduced and chemical which may be consumed is not replaced. However, in the beaker test, the nylon loop is surrounded constantly and uniformly by a surplus of hot chemical solution of practically the same concentration throughout the duration of the test thus allowing the chemical to function more effectively.
The following examples will further illustrate the embodiment of this invention. In these examples, all parts given are by weight unless otherwise noted.
EXAMPLE] The shrinkage and weight loss experienced by a test loop of DuPont type 846 bulk continuous filament nylon 6/6 (1300 denier, 68 filaments, o twist, semi-dull, regular acid dyeable) was determined by means of the beaker test procedure described in Table 1 using the following aqueous recipes comprising 50 percent thiourea and various concentrations of formic acid. Test temperature and duration was about 215 F (102C) and 30 minutes respectively, except for water alone where the test temperature was 212 F (100 C). Test results are recorded in Table 11.
It was found that the combination of 50 percent thioor be dispersible to an extremely finely divided condition so that the individual particles contained in the room temperature printing paste can pass through the printing screen and reach a maximum area of the nylon fiber to develop the desired effect. Preferably the solubilizing medium should be mostly water although other solvents may be utilized. 50 percent thiourea is readily soluble in hot water or the hot acid solution at about 180 F. (82 C), but is soluble to the extent of only about 15 percent at room temperature. When the level of thiourea is reduced to 15 percent to gain room temperature solubility, the combination of 15 percent thiourea with 15 percent and 33.3 percent formic acid percent) respectively produces only minimal shrinkage of 14.3 percent and 25.2 percent (Run Nos. 51 and 56). Formic acid alone at 30 percent concentration produces 16.6 percent shrinkage (Run No.
From the foregoing tests, it is apparent that 50 percent thiourea, by weight, in water accompanied by 10-16 percent acid, by weight, such as 90 percent formic acid, 85 percent phosphoric acid, acetic acid, 37 percent hydrochloric acid, oxalic acid, 2-naphthalenesulfonic acid will induce shrinkage approaching 50 percent or more in the nylon fibers. It is, of course, important that the fibers remain physically fibers and that the shrunk filaments and tufts retain their original physical character, appearance, and acceptable feel.
TABLE 111 Nylon Filament Shrlnk- Weight Run age Loss Loop No. Chemicals Character l5,17,30,35 avg. Water 10.0 1.50 Good 59 Thiourea, 50%/85% Phosphoric Acid, 45.2 I 1.0 Good 129 Thiourea, SOZ /Acetic Acid, 15% 54.2 13.9 Good 48 Thiourea. 5091/37; HCl, 16% 40.6 106 Good 43 Thiourea, SOXr/Oxalic Acid, 20.7 1.71 Good 661 Thiourea. SOZ /Oxalic Acid, 15% 40.0 8.68 Good 108 Thiourea, 40%IZ-Naphthalenesulfonic 43.5 8 9 Good Acid, 10% 135 Thiourea, SOX /Trichloroacetic Acid, 31.1 2.44 Good 5; 62,133 avg. Thiourea, 50%lMonochloroacetic Acid, 16.3 1.14 Good 61 Thiourea, SO'Z/Zinc Chloride, 16.7 33.4 4.1 Good 137 85% Phosphoric Acid, 15% 12.3 +1.09 Good 136 Acetic Acid, 15% 12.5 0.53 Good 141 37% Hydrochloric Acid, 16% 13.9 2.75 Good 138 Oxalic Acid, 15% 14.3 +0.71 Good 98 Z-Naphthalenesulfonic Acid, 10% 26.0 2.11 Good 49 90% Formic Acid, 15% 9.4 1.41 Good 134 Trichloroacetic Acid, 5% 19.8 0.66 Good 70 Monochloroacetic Acid, 29.3 2.71 Good 27 Zinc Chloride. 35% 23.3 2.06 Good EXAMPLE ll 25 and proportion of chemicals used. Data also indicate that the dimethylthiourea/formic acid system has a strong potential as an embossing agent for nylon carpet The Shrinkage and weight 1 developed by a test being capable of causing fiber distegration within 60 l f p type 34 bulk continuous fil t seconds in the beaker test. When dimethylthiurea is nylon 6/6 1300 denier, 68 filaments, 0 twist, semi-d ll, used alone at percent and percent concentration, regular acid dyeable) was determined by means of beathe shrinkage induced amounts to 18.0 percent and ker test procedure described in Table 1 using the fol- 31.3 percent respectively (R n N0 14 n nlowing aqueous recipes containing the readily room sufficient for carpet embossment. Similarly, when temperature water soluble dialkyl derivative of thiopercent formic acid is used alone even at 33.3 percent urea, 1,3 dimethylthiourea, in combination with for- 35 (Run No. 150) it yields only 16.6 percent shrinkage. mic acid. The test temperature and maximum duration these results may be compared to the 10 percent of test was 215 F l 0 2 C and l5 rnjnut e s respecshrinkage obtained withwater alone.
TABLE IV Nylon Filament Shrink- Weight Run age Loss Loop No. Chemicals Characters l5,l7,30,35 avg. Water 10.0 1.5 Good Dimcthylthiourea, 35% 18.0 1.62 Good 186 Dimethylthiourea, 60% 31.3 5.89 Good 90% Formic Acid, 333% 16.6 0.67 Good 54 90% Formic Acid, 15% 9.4 1.4] Good 120,122 avg. DMT, 50%lFormic, 15% 73.5 44.7 Fragile 124 DMT, 35%lFormic, 15% 35.7 3.74 Good 125 DMT, 40%lFormic, 20% 81.1 55.8 Fragile 126 DMT, 40%lFormic, 15% 42.9 8.44 Good 142 DMT, 35%/Formic, 22.3% 51.3 11.7 Good 146,233 avg. DMT, 35%lFormic, 27.7% Disintegrate 60 sec. DMT. 40%lFormic, 20% 67.9 35.6 Fragile 187 DMT, 35%lFormic, 33.3% Disintegrate 5 sec. 188 DMT, 40%/Formic, 22.3% Disintegrate 5 sec. 189 DMT, 40%/Formic, 27.7% Disintegrate 5 sec. 190 DMT, 45%lFormic, 16.7% 69.0 32.4 Weak 191 DMT, 45%lFormic, 22.3% Disintegratc 10 sec. 192 DMT, 50%/Formic, 16.7 Disintegrate 60 sec. 193 DMT, 30%lFormic, 33.3% Disintegrate 20 sec. 194 DMT. 30%lFormic 27.7% 73.0 37.6 Fragile While formic acid is the preferred acid, other acids Data in Table IV show that chemical compositions may be used in conjunction with dimethylthiourea with comprising dimethylthiourea (DMT) and formic acid results as shown in Table V. Acids which allow room can produce effects on nylon fibers ranging from strong 65 temperature water solubility of the dimethylthiourea/atively. Test results are shown in Table IV.
shrinkage without fiber deterioration (about 50 percent) e.g., Run No. 142 to immediate disintegration e.g., Run lilo. 233 depending upon the concentration cid combination and which generally function quite strongly, but less effectively than formic acid in the shrinking system include acetic, phosphoric, malonic,
citric, propionic, citraconic, benzenephosphonic, phenolsulfonic, toluenesulfonic and naphthalene sulfonic acids, and combination thereof.
Again, it is apparent that these chemical agents are capable of strongly shrinking nylon fibers.
TABLE V Nylon Filament Shrink- Weight Run age Loss Loop No. Chemicals Character 219 DMT, 35%/Hydroxyacetic Acid, 25% 30.0 4.3 Good 220 DMT, 35%/Monochl0roacetic Acid, 25% 15.5 +2.05 Good 221'" DMT, 35%/Maleic Acid, 251 lnsol. at 220F (103C) 235" DMT, 35%/Maleic Acid. 41.6 4.79 Good 222" DMT, 35%/oxalic Acid, Anhyd., 25% Disintegrate sec. 224" DMT, 35%/oxalic Acid, 2H20, Fragmented 15 min. 223 DMT, %/Mu10nic Acid, 25% 46.5 10.8 Good 241 DMT, %lMal0nic Acid, 25% 59.0 21.4 Wcak 242 DMT, 35%/Malonic Acid. 30% 83.2 58.6 Fragile 244 Malonic Acid. 35% 18.0 1.61 Good 247 DMT, 35%/Malonic Acid, 35% Disintegrate 15 sec. 225 DMT, 35%/Gluconic Acid, 25% 18.2 +0.54 Good 226 DMT, 35%/Maleic Acid, 25% 36.3 5.85 Good 227 DMT, 35%/Phenolsulfonic Acid, 15% Disintegrate 2 min. 236 DMT, 37.5%lPhenolsulfonic Acid, 12.5% 45.2 8.5 Good 229 DMT, 35%/Naphthalenesulfonic Acid, 15% Disintegrate 15 min. 237 DMT, 37.5%lNaphthalenesulfonic Acid. 63.0 28.4 Fragile 12.5% 230 DMT, 35%/'loluenesulfonic Acid, 15% 70.9 39.1 Fragile 231 DMT, 35%/Sulfamic Acid. 25% 30.3 1.45 Good 240** DMT, 35%/Sulfamic Acid, 25% lnsol. at 220F 232* DMT. 35%/Glutamic Acid HCI, 25% lnsol. at 220F (103C) 234 DMT, 35%/Benzenephosphonic Acid, 25% Disintegrate 2 /4 min. 243 Benzenephosphonic Acid, 35% 73.0 10.5 Fragile 239 DMT, 35%/Citric Acid, 25% 40.6 6.18 Good 245 DMT, 35%/Citric Acid, 30% 56.6 14.4 Good 92 Citric Acid, 23.8 +4.03 Good 238 DMT, 35%/Tartaric Acid, 25% 29.2 3.57 Good 250 DMT, 35%/Levu1inic Acid, 25% 26.4 3.24 Good 251 DMT, 25%/Acetic Acid, 25% 65.5 28.9 Weak 290 DMT, 35%/Acetic Acid, 30% Mostly disintegrated sec. 354 DMT, 25%/Acetic Acid, 35% Mostly disintegrated 15 min. 396 DMT, 40%lAcetic Acid, 25% Disintegrate 40 sec. 397 DMT, 35%/Acetic Acid, 35% Disintegrate 20 sec. 294 DMT, 35%/Acetic Acid, 22.5%/90% For- Partial Disintegrate 15 min.
mic Acid, 2.5% 297 DMT, 35%/Acetic Acid, 22.5%lSulfuric Disintegrate 2 min.
Acid 2.5% 253 DMT, 35%/Acetic Acid, 18.7%/% Fragmented 15 min.
Phosphoric Acid, 63% 252 DMT, 35%/Lactic Acid, 25% 37.1 6.87 Good 288 DMT, 35%/Propionic Acid, 25% 77.6 41.3 Fragile 289 DMT, 35%/Citraconic Acid, 25% 69.6 30.8 Fragile 143 DMT, 35%/85% Phosphoric Acid, 23.7% 42.4 8.15 Good 149 DMT, 35%/85% Phosphoric Acid, 29.3% Fragmented 15 min. 151 85% Phosphoric Acid, 29.3% 16.5 +2.36 Good 'DMT Dimcthyllhiuurca "insoluble at room temperature EXAMPLE 111 55 RUN NO. 7333? This example illustrates the preparation of an em- M r p Gram, bossed pile fabric typical of the products of this invention 1. Water 20.1 2. Cibaphasol AS 0.5 A defined geometric area of nylon carpet was treated 3. Antifoam 73 0.8 by means of a screen printing technique with a dye 60 g- 345 32 32 A 132 print paste containing 30 percent dimethylthiourea and 6. Dimethylthiourea 30.0 30.6 percent formic acid percent), by weight, as Y 005 the embossing agent.
Carpet construction was as follows:
Type percent nylon 6/6 spun yarn non heat set 65 The dye print paste was formulated as follows:
'2 Sulfuric Acid ester, levelling and penetrating agent.
3 Alcohol ester, antifnaming agcnt. P 4 Xantl an gum thickener lus DowjcideA preservative yields a Brevokfield viscosity of 550cm. at 7 8f (No. 3 spindle. 2% rpm). 6 Add dimcthylthiourca to thc formic acid solution to facilitate solubility.
" Hrookfield No. 3 spindle. 292 rpm. 78F
There was no evidence of embossing while the nylon carpet was held at room temperature for several minutes. Upon subjecting the carpet to steaming for 15 minutes at about 220 F 104 C), significant emboss ing due to fiber shrinkage was observed. Thereafter, the embossed carpet was thoroughly rinsed with water 7 and dried. The rinsing removed residual chemicals.
The resulting carpet exhibited good embossment with a 50 percent reduction in pile height in the treated area in perfect register with the printed design. Despite this degree of shrinkage, the nylon tufts retained their individuality and while increasing in firmness remained adequately soft, and showed no significant deterioration ofphysical properties. MA 7 W" Again, while formic acid is the preferred acid to use with dimethylthiourea, other acids may be employed. Table VI shows results obtained with formic acid, acetic acid, and phosphoric acid used in combination with dimethylthiourea, as well as the effect of changing concentrations and proportions in the dimethylthiourea system. In some cases corresponding beaker test results are shown. Phosphoric acid is generally unsatisfactory since it deteriorates fibers. As noted previously, a beaker test shrinkage of approximately 50 percent is equivare very effective in acid solution (preferably formic acid) as shrinking agents for nylon fibers. Depending upon the ratio and concentration of thiourea derivative and acid, effects are produced ranging from strong shrinkage of the nylon fiber in 15 minutes to total disintegration within a few seconds. This latter effect signifies that the proper combination of dimethylethylthiourea or trimethylthiourea and an acid has the capability of embossing nylon carpet deeply.
It will be observed that the individual concentrations employed, neither of theses derivatives of thiourea alone, or the acid alone, produce sufficient shrinkage of the nylon filament to produce carpet embossment.
Usually at least 50 percent shrinkage of the nylon filaalent to barely perceptible carpet embossment. Fiber 25 w disintegration within approximately 1 minute is gener- Mmeflfl" Grams ally required to provide a chemical embossing agent Walter 174 concentration which yields significant carpet emboss- 2. Clbuphflsul 3. Antifoam 73 0.8 ment. Thus, it is apparent that the concentration and 30 44 Kelzan NW7) (01% Dowicide A) 210 proportion of dlmethylthiourea to acid must be prop- Fmmic Acid (907,) 333 erly adjusted to yield a desired depth of embossment glmcthylcthyllhioureu 3.8 C without deterioration of the nylon fibers. y MW TABLE VI Embossing System Beaker Test Nvlon Filament Nvlon Carpet Shrink- Wgt. Loop Paste" bogged T fl Run in Time age Loss Charvisc. Depth Char- No. Chemicals Paste (Mins) (7!) ("/r) acter (cps) actor 1421 DMT90'7r Formic 35/222 15 57.7 22.2 Weak 320 10 Uneven, good |49l DMT/XSZ Phosphoric 3l.8/26.7 52.3 [1.9 Good 720 Trace Good l49l-2 DMT/85Z Phosphoric 35/294 4 Disintegrate 240 -75 Uneven, weak l54SP DMT/JOZ Formic /27.8 l Disintegrate 680 29 Good l55sP DMT/Acctic 35/25 15 54.4 176 Good 720 10 Good 1568? DMT/JOZ Formic /333 480 80 Hard, stiff harsh I57SP DMTIQOZ Formic 37.5/3l.2 l Disintegrate 480 Harsh, brittle ZIOSP DMT/85'z Phosphoric 35/29.4 2520 25 Brittle 212SP DMT/QO'Z Formic 35/271! 640 30 Good 213SP DMT/QU'Z Formic 35/27.8 4400 30 Good 3l3SP DMT/Acctic 35/30 960 19 Good 397SP DMT/Acetic 35/35 I040 41 Brittle Dimethylthiourca (DM'I') Acid EXAMPLE IV The shrinkage and weight loss developed by a test loop of DuPont type 846 bulk continuous filament nylon 6/6 (1300 denier, 68 filaments, 0 twist, semi-dull, regular acid dyeable) was determined by means of the beaker test procedure described in Table I using the aqueous recipes shown in Table Vll containing dimethylethylthiourea of trimethylthiourea in combination with formic acid or acetic acid. Both of these derivatives of thiourea are soluble in acid solution at room temperature. The test temperature and maximum duration of test was 215 F) and 15 minutes respectively. Test results are shown in Table VII.
As can be seen from the test data, both trimethylthiourea and particularly dimethylethylthiourea (a liquid) 4 Sulfuric acid ester. levelling and penetrating agent.
3 Alcohol ethcr. antifouming agent.
4 Xunthan gum lhickncr plus preservative in water providing a Brookfield viscosity of 600 cps. at 78F (No. 3 spindle, 2% rpm.).
There was no indication of embossing while the nylon carpet remainded at room conditions for several minutes. Upon subjecting the carpet to steaming for 15 7 ourea/acid embossing agent system are used alone, the
effect on nylon shrinkage is not much greater than water alone.
TABLE V11 fiylmi lawfi Shrink- Weight Run age Loss Loop Ni. (,hemiezrls (7') ('70 Character 15, 17, .50 35 avg. Water (tap), 100% 10.0 1.5 Good 150 Formic Acid, 30% 16.6 0.67 Good 159 Formic Acid, 40% 31.3 2.98 Good 357 Acetic Acid, 30% 13.5 1.06 Good 659 Acetic Acid, 45% 27.0 3.92 Good 889 DMET, 30% 19.3 +0.62 Good 893 TMT, 30% 15.7 0.37 Good 873 DMET, 25%lFormic Acid, 25% 79.2 26.7 Fragile 805 DMET, 30%/Formic Acid, 275% Disintegrate 4 seconds 887 DMET, 15%lFormic Acid, 40% Disintegrate 2 seconds 888 DMET, 10%lFormic Acid, 30% 40.2 3.57 Good 872 DMET, 30%/Acetic Acid, 30% 58.3 20.3 Weak 885 DMET, %/Acetic Acid, 45% Fragmented 15 minutes 869 TMT, %lFormic Acid, 27.5% Disintegrated 10 seconds 886 TMT, 25%/Formic Acid, 25% 64.8 18.7 Weak DMET Dimethylcthylthiourea (liquid) TM'l' Trimcthylthiourea (solid) Preferably add lhiourea derivative to acid solution to speed solubility. immiscible with water at room temperature and 2l5F Insoluble at room temperature. Some insoluble at 215F EXAMPLE V EXAMPLE V1 The shrinkage and weight loss experienced by a test loop f DuPont type 34 bulk continuous fil m t The nylon carpet construction cited in Example 111 nylon 6/6 1300 denier, 68 filaments,o twist, semi-dull, 35 was 8 treated y means of a Screen Prmung techregular acid dyeable) was determined by means of the beaker test procedure described in Table 1 using the following recipes containing 1,3 diethylthiourea and an acid such as formic acid and acetic acid. The test temperature was 215F 102C) for a maximum time of 15 minutes. Results are tabulated in Table V111.
These data show that a chemical composition comprising diethylthiourea and an acid such as formic acid or acetic acid can cause effects on nylon fibers ranging from strong shrinkage, about 50 percent without fiber deterioration, to immediate fiber disintegration depending upon the concentration and proportion of the chemicals used. Further, these results indicate that the diethylthiourea acid combination is a potentially strong embossing agent for nylon carpet.
At the concentration employed, diethylthiourea is largely insoluble in water alone or in formic acid at room temperature. Thus, when diethylthiourea is used with formic acid, a portion of a water miscible solvent such as isopropyl alcohol, cellosolve acetate or cellosolve solvent is used to provide a solvent system at room temperature. But in the case of the diethy1thiourea/acid system, acetic acid serves as an excellent solubilizing agent for diethylthiourea as well as shrinkage of the nylon filament. Consequently, acetic acid is the preferred acid to be used in conjunction with diethylthiourea. Observe also that a combination of dimethylthiourea and diethylthiourea may also be used effectively with an acid such as formic acid. (Run No. 180.) Again, it will be observed from the data in Table V111, that when the. components of the diethylthinique. However, in this case the embossing agent comprised a dye print paste containing diethylthiourea 25 percent and acetic acid 35 percent, by weight. It will be noted that similar proportions in the beaker test caused the nylon filament loop to disintegrate within 30 seconds at 215F. (Run No. 351-, Table V111.)
The print paste recipe was as follows:
RUN NO. 3515? Materials Grams Water 17.2 Cibaphasol AS 1.0 Antifoam No. 73 0.8 Kelzan (l /2%) 0.2% Dowicide A 21.0 Acetic Acid 35.0 Diethylthiourea 25.0 Dye 0.05
' Add diethylthiourea to acetic acid solution to facilitate solubility.
Nylon Filament Shrink- Weight Run age Loss Loop No. Chemicals Character Water 10.5 1.27 Good 150 90% Formic Acid, 33.3% 16.6 0.67 Good 357 Acetic Acid. 30% 13.5 106 Good 659 Acetic Acid, 45% 27.0 3.92 Good 176 Diethylthiourea. 40% Insoluble at 220F 660 DET, 40%lCellosolve Solvent, 20% 20.9 0.54 Good 172 DET, 40%/90% Formic Acid, 20% Disintegrate sec. 179 DET. 30%/90% Formic Acid, 16.7% 69.4 6.5 Fragile 180 DET, %IDMT, l0%/90% Formic Acid, 22.3% 62.1 15.3 Weak 181 DET, 30%/90% Formic Acid, 16.7%!
lsopropyl Alcohol, 16.7% 50.7 13.3 Good 196 DET, 30%/90% Formic Acid, 16.7%]
Cellosolve Acetate 26.7% 52.3 19.8 Good 205 DET, 30%/90% Formic Acid, l6.7%/
Cellosolve Solvent 20% 47.8 119 Good 206 DET, 40%/90% Formic Acid, 20%/ Cellosolve Solvent 20% Disintegrate 15 sec. 341" DET, %lAcetic Acid, Brittle 15 mins. 350*" DET, 30%/Acetic Acid, 30% Disintegrate 60 sec. 351" DET, 25%lAcetic Acid, Disintegrate 30 sec. 352" DET, 20%lAcetic Acid, Partial Disintegrate 15 min. 410" DET, 30%/Acetic Acid, 35% Disintegrate 15 sec. 422" DET, l5%/Acetic Acid, Fragment sec.
' DET dietthylthiourca. DMT dimethylthioureu Avg. of I3 runs. Dissolve DET in acid EXAMPLE Vll The shrinkage and weight loss experienced by a test loop of DuPont type 846 bulk continuous filament nylon 6/6 1300 denier, 68 filaments, o twist, semi-dull,
urea and an acid such as formic. All of these derivatives were largely insoluble in water at room temperature requiring a temperature in the neighborhood of 200F (C) to solubilize at the concentration employed. Tests were conducted for 15 minutes at 215220F (102 105C). Results are recorded in Table lX.
N-acetylthiourea, 1,3 diisopropyl-thiourea and ethylene-thiourea with formic acid showed a capability for nylon fiber shrinkage. The 1,3 dihydroxyethylethylene thiourea had little effect.
In recapitulation, it is to be understood that the process of embossed carpet involves manipulation corresponding to that of printing a pattern on the carpet. Where mesh embossment is sought the printed composition is colorless. Where the design combines color with the embossment a dye paste is the vehicle generally, whether the operation be a mere embossment or an embossment combined with dyeing. It is preferred that there be no shrinkage of the nylon fibers at ambient temperatures, even up to 50C. In plant operations the delay from printing to steaming may be as much as 8-10 minutes. Hence, if there is no significant effect on the material at temperatures below 50C for 15 20 minutes there is ample time for operations. That is, activation of the shrinkage is reserved for the stage where the printed material enters the steaming operation. In standard carpet handling the steaming is a 10 20 minute operation to fix the dye and in this stage the embossing is completed in the first few minutes.
For effective embossment there should be at least perceptible shrinkage in the tufts. Generally, penetration of the embossing print paste will be of the order of 50 75 percent. Where it is desired to have full depth coloration of the printed area uniformly to the back of the fabric, this can be accomplished by predying the carpet completely to the back by means of an operation such as pad dyeing. It should be apparent that in operations where mere embossment is sought there is no significant problem in the placement of the design on the fabric. Where embossment is combined with a multicolored print there is the register problem and the color area will be in perfect register with the embossed design when the shrinkage agent is combined with the color paste as set forth in detail in the examples.
TABLE 1X Nylon Filament Acid, 15%
' avg. of 13 runs In the production of the pile fabrics of this invention, the pile yarn employed is prepared from fiber-forming iylllllcllC linear polyamides. Examples of these fiberluruiing synthetic linear polyamides are those obtainable from polymerizable monoaminomonocarboxylic acids and their amide-forming derivatives including caprolactam and those obtainable from the reaction of suitable diamines with suitable dibasic carboxylic acids or their amide-forming derivatives. Such synthetic linear polyamides are referred to as nylon.
Nylon or polyamide polymers, filaments and fibers are well known to those skilled in the art and extensive discussion is, therefore, unnecessary. Thus the term polyamide or nylon is known to include any long chain synthetic polymeric amide which has recurring amide groups as an integral part of the main polymer chain and which is capable of being formed into a filament in which the structural elements are oriented in the direction of the axis of that chain.
Polyamide resins coming within this definition and are nylon-6,6, prepeared by the condensation of hexa- 25 methylenediamine and adipic acid; nylon-6,l0, prepared from hexamethylenediamine and sebacic acid, both of the foregoing having, as prepared, molecular weights exceeding 10,000: nylon-6 produced by thermal polymerization of epsilon-aminocaproic acid or caprolactam; nylon-l l, the self-condensation product of ll-aminoundecanoic acid; as well as a variety of polymers prepared from polymerized, unsaturated fatty acids and polyamino compounds.
The practice of the present invention has, however, particular application to solid melt-extrudable and orientable fiber-forming polyamides and more particularly to fibers and filaments prepared therefrom which have a denier and tenacity appropriate, and well known to those skilled in the art, for use in carpet, rugs, tapestry and the like. Illustrative of these polyamides are those having a filament denier of 2-30 or higher or nylon yarns in the denier range of l-l 5,000 or higher. The tenacities of nylon yarn for use herein are within the range of 3-l0 grams per denier. The elongation of commercial fibers can range between l6 and 65 percent. The undrawn filament is capable of being stretched as much as 5 times. [t is understood additionally that encompassed within the polyamides that can be employed in the practice of this invention are high molecular weight synthetic linear polyamides, in addition to those described hereinabove, that have been modified. for example, to enhance their usefulness for particular applications.
An extended discussion of polyamides of sufficiently high molecular weight to be capable of being melt spun into filaments and co ming within the contemplation of this invention appears in DE Floyd, Polyamide Resins, Reinhold Plastics Applications Series, Reinhold Publishing Corporation, New York, New York, (2nd Printing 1961), and HR. Mauersberger, Matthews Textile Chemical Properties, John Wiley & Sons, Inc., New York, New York, pp. 933-971, 1034., (6th ed. 1954), Mary E. Carter, Essential Fiber Chemistry, Marcel Dekker, lnc., New York 1971, pp. 91-109, and HF Mark, S.M. Atlas, E. Cernia (Edited by), Man-Made applying to defined areas of the pile surface of said fabric a chemical embossing agent for said fibers, said agent being blended into a liquid base vehicle and corresponding to the following formula:
R-N-C-NH-R" wherein R, R and R" may be any combination of H, N-acetyl, methyl, ethyl, butyl, isopropyl, pentyl, or hexyl, said aqueous base vehicle also including an acid,
allowing said embossing agent in its vehicle to remain in contact with said fibers for a period of time and at a temperature sufficient to reduce the height of said pile, without deterioration of said fibers and, thereafter, effectively removing the embossing agent from the fabric,
said reduction in height of the fibersbeing in the area contacted by said embossing agent only and being a reduction sufficient to display a significant embossed effect in the overall fabric.
2. The process of claim 1 wherein said embossing 40 agent is dimethylthiourea with formic acid in concentrations of 5 per cent to 60 per cent dimethylthiourea and 10 per cent to 50 per cent formic acid, by weight, of total embossing composition.
3. The process of claim 2 wherein said embossing agent is incorporated in a transparent vehicle therefor.
4. The process of claim 2 wherein said embossed effect is made in register with a printed color design on said fabric and said vehicle is a dye printing paste carrying said embossing agent.
5. The process of claim 2 wherein said embossing action occurs within approximately 15 minutes at a temperature above 50C.
6. The process in accordance with claim 5 wherein said embossing action occurs in a steam environment.
7. The process of claim 6 wherein said embossing composition is present in a concentration of about 55 to 70 per cent in the vehicle therefor.
8. The process of claim 7 wherein said embossing agent is thiourea and formic acid.
9. The process of claim 7 wherein said embossing agent is dimethylthiourea and acetic acid.
10. The process of claim 7 wherein said embossing agent is dimethylthiourea and phosphoric acid.
11. The process of claim 7 wherein said embossing agent is dimethylthiourea and oxalic acid.
12. The process of claim 7 wherein said embossing agent is dimethylthiourea and hydrochloric acid.
13. The process of claim 7 wherein said embossing agent is diethylthiourea and formic acid.
14. The process of claim 7 wherein said embossing agent is diethylthiourea and acetic acid.
15. The process of claim 7 wherein said embossing agent is diethylthiourea and phosphoric acid.
agent is trimethylthiourea and formic acid.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US556794 *||Nov 18, 1895||Mar 24, 1896||Sue-sagne|
|US1223018 *||Mar 8, 1915||Apr 17, 1917||Eduard Zeidler||Process for manufacturing fancy webs having raised designs.|
|US1655414 *||Oct 9, 1925||Jan 10, 1928||Henry Flory||Method and chemical mixture for producing brocaded textiles|
|US1834339 *||May 3, 1928||Dec 1, 1931||Celanese Corp||Treatment of textile materials containing carbonizable fibers and product thereof|
|US2020698 *||Oct 24, 1933||Nov 12, 1935||Celanese Corp||Pile fabric and method of treating the same|
|US2875504 *||May 13, 1957||Mar 3, 1959||Collins & Aikman Corp||Methods of processing pile fabrics|
|US2901373 *||Mar 12, 1957||Aug 25, 1959||Heberlein Patent Corp||Pattern flock fabric and methods for producing said pattern|
|US3567548 *||May 12, 1967||Mar 2, 1971||Phillip Miller||Production of permanently sculptured pile fabrics|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3989448 *||Apr 12, 1974||Nov 2, 1976||Armstrong Cork Company||Overprint of solvent on total solvent coating|
|US4112560 *||Dec 15, 1976||Sep 12, 1978||Milliken Research Corporation||Method for sculpturing pile fabrics|
|US4129416 *||Jun 28, 1977||Dec 12, 1978||Armstrong Cork Company||Process for shrinking nylon fabrics|
|US4174664 *||May 8, 1978||Nov 20, 1979||Milliken Research Corporation||Cylindrical screen having aperatures with geometric centers defined by arrays of equilateral triangles|
|US4215987 *||Dec 11, 1978||Aug 5, 1980||Cotton Incorporated||Process for chemically imparting a durable, multiple-level, pile height to terry towelling, terry fabric and cut pile cotton fabric|
|US4255231 *||Jun 13, 1979||Mar 10, 1981||Congoleum Corporation||Carpet etching|
|US4260390 *||Dec 10, 1979||Apr 7, 1981||Armstrong Cork Company||Additive-solvent process to form embossed product|
|US4286955 *||Jul 30, 1979||Sep 1, 1981||Armstrong Cork Company||Fiber shrinking composition for nylon pile fabric|
|US5417754 *||Dec 22, 1993||May 23, 1995||Hester; Michele L.||Composition and method for selective removal of fabric design image|
|US6832419 *||Jul 3, 2003||Dec 21, 2004||Milliken & Company||Method of making pile fabric|
|US7229680||Sep 21, 2000||Jun 12, 2007||Microfibres, Inc.||Realistically textured printed flocked fabrics and methods for making the fabrics|
|US7423002||Jun 6, 2006||Sep 9, 2008||S.C. Johnson & Son, Inc.||Method of neutralizing a stain on a surface|
|US7435264 *||Nov 12, 2003||Oct 14, 2008||Milliken & Company||Sculptured and etched textile having shade contrast corresponding to surface etched regions|
|US7556841||Jun 6, 2006||Jul 7, 2009||S. C. Johnson & Son, Inc.||Method of applying a design to a surface|
|US7575027 *||Jan 5, 2007||Aug 18, 2009||Min-San Huang||Weave with visual color variation|
|US7727289||May 14, 2008||Jun 1, 2010||S.C. Johnson & Son, Inc.||Composition for application to a surface|
|US7776108||Jun 24, 2009||Aug 17, 2010||S.C. Johnson & Son, Inc.||Composition for application to a surface|
|US8061269||May 14, 2008||Nov 22, 2011||S.C. Johnson & Son, Inc.||Multilayer stencils for applying a design to a surface|
|US8499689||Sep 14, 2011||Aug 6, 2013||S. C. Johnson & Son, Inc.||Kit including multilayer stencil for applying a design to a surface|
|US8557758||Oct 28, 2010||Oct 15, 2013||S.C. Johnson & Son, Inc.||Devices for applying a colorant to a surface|
|US8728581||Jul 19, 2010||May 20, 2014||Columbia Insurance Company||Embossed carpet backing|
|US8734533||Jun 21, 2010||May 27, 2014||S.C. Johnson & Son, Inc.||Composition for application to a surface|
|US8747487||Oct 21, 2010||Jun 10, 2014||S.C. Johnson & Son, Inc.||Composition for application to a surface|
|US8846154||May 6, 2011||Sep 30, 2014||S.C. Johnson & Son, Inc.||Carpet décor and setting solution compositions|
|US9593443||Nov 25, 2013||Mar 14, 2017||Crayola Llc||Compositions and methods for embossing and debossing fabrics|
|US20040253408 *||Jun 12, 2003||Dec 16, 2004||Burlington Industries, Inc.||Variable optical effect textile|
|US20050000070 *||Jul 3, 2003||Jan 6, 2005||Williamson Curtis Brian||Method of making pile fabric|
|US20050100705 *||Nov 12, 2003||May 12, 2005||Mark Kiff||Sculptured and etched textile having shade contrast corresponding to surface etched regions|
|US20080010793 *||Jul 3, 2006||Jan 17, 2008||Martin Wildeman||Textile fabric with variable heat-shrunk yarn constituents|
|US20080163952 *||Jan 5, 2007||Jul 10, 2008||Min-San Huang||Weave with visual color variation|
|US20100256263 *||Jun 21, 2010||Oct 7, 2010||S.C. Johnson & Son, Inc.||Composition for application to a surface|
|US20110038826 *||Oct 21, 2010||Feb 17, 2011||S.C. Johnson & Son, Inc.||Composition for application to a surface|
|USB460388 *||Apr 12, 1974||Jan 27, 1976||Title not available|
|EP1684974A2 *||Aug 31, 2004||Aug 2, 2006||Milliken & Company||Sculptured and etched textile having shade contrast corresponding to surface etched regions|
|EP1684974A4 *||Aug 31, 2004||Jun 25, 2008||Milliken & Co||Sculptured and etched textile having shade contrast corresponding to surface etched regions|
|WO2005057487A2||Aug 31, 2004||Jun 23, 2005||Milliken & Company||Sculptured and etched textile having shade contrast corresponding to surface etched regions|
|WO2006133169A2 *||Jun 6, 2006||Dec 14, 2006||S. C. Johnson & Son, Inc.||Composition for application to a surface|
|WO2006133169A3 *||Jun 6, 2006||May 31, 2007||Johnson & Son Inc S C||Composition for application to a surface|
|U.S. Classification||8/497, 26/69.00B, 8/598, 156/277, 8/924, 28/160, 8/929, 8/585|
|Cooperative Classification||Y10S8/924, D06Q1/06, Y10S8/929|
|Nov 14, 1994||AS||Assignment|
Owner name: CONGOLEUM CORPORATION, NEW JERSEY
Free format text: TERMINATION OF SECURITY AGREEMENT;ASSIGNOR:CIT GROUP/BUSINESS CREDIT, INC., THE, AS AGENT;REEL/FRAME:007205/0471
Effective date: 19941026
|May 9, 1991||AS||Assignment|
Owner name: CIT GROUP/BUSINESS CREDIT, INC., THE, AS AGENT
Free format text: SECURITY INTEREST;ASSIGNOR:CONGOLEUM CORPORATION A CORP. OF DE;REEL/FRAME:005805/0833
Effective date: 19910419
|May 9, 1991||AS06||Security interest|
Owner name: CIT GROUP/BUSINESS CREDIT, INC., THE, AS AGENT
Owner name: CONGOLEUM CORPORATION A CORP. OF DE
Effective date: 19910419
|Aug 5, 1986||AS02||Assignment of assignor's interest|
Owner name: CONGOLEUM CORPORATION, 195 BELGROVE DRIVE, KEARNY,
Effective date: 19860621
Owner name: CONGOLEUM CORPORATION, A CORP OF DE. ORGANIZED IN
|Aug 5, 1986||AS||Assignment|
Owner name: CONGOLEUM CORPORATION, 195 BELGROVE DRIVE, KEARNY,
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:CONGOLEUM CORPORATION, A CORP OF DE. ORGANIZED IN 1984;REEL/FRAME:004598/0171
Effective date: 19860621
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CONGOLEUM CORPORATION, A CORP OF DE. ORGANIZED IN 1984;REEL/FRAME:004598/0171
Owner name: CONGOLEUM CORPORATION, A CORP. OF DE., ORGANIZED I
|Aug 6, 1984||AS||Assignment|
Owner name: CONGOLEUM CORPORATION
Free format text: CHANGE OF NAME;ASSIGNOR:N & R FUNDING CORPORATION;REEL/FRAME:004300/0182
Effective date: 19840604
Owner name: N & R FUNDING CORP., 976 MARKET STREET EXTENSION,
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:CONGOLEUM CORPORATION A CORP. OF DE;REEL/FRAME:004300/0888
Effective date: 19840601
|Aug 6, 1984||AS02||Assignment of assignor's interest|
Owner name: CONGOLEUM CORPORATION A CORP. OF DE
Owner name: N & R FUNDING CORP., 976 MARKET STREET EXTENSION,
Effective date: 19840601