US3420701A - Process for imparting rot-resistance to an organic textile material and the resulting material - Google Patents
Process for imparting rot-resistance to an organic textile material and the resulting material Download PDFInfo
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- US3420701A US3420701A US3420701DA US3420701A US 3420701 A US3420701 A US 3420701A US 3420701D A US3420701D A US 3420701DA US 3420701 A US3420701 A US 3420701A
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- organic
- organolead
- fibrous material
- rot
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- 238000000034 method Methods 0.000 title claims description 26
- 239000000463 material Substances 0.000 title description 11
- 239000004753 textile Substances 0.000 title description 11
- 239000000243 solution Substances 0.000 claims description 39
- 239000002657 fibrous material Substances 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 15
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 11
- 239000011368 organic material Substances 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 150000001450 anions Chemical class 0.000 claims description 4
- 238000009877 rendering Methods 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- 229920000742 Cotton Polymers 0.000 description 12
- 239000000126 substance Substances 0.000 description 11
- 238000009933 burial Methods 0.000 description 9
- 239000002689 soil Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 230000000717 retained effect Effects 0.000 description 8
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- KMVZRJYWOGEEQJ-UHFFFAOYSA-N tributyl(imidazol-1-yl)plumbane Chemical compound CCCC[Pb](CCCC)(CCCC)N1C=CN=C1 KMVZRJYWOGEEQJ-UHFFFAOYSA-N 0.000 description 6
- 239000001768 carboxy methyl cellulose Substances 0.000 description 5
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 5
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 4
- 229940070765 laurate Drugs 0.000 description 4
- LMDKALUFKHCRFQ-UHFFFAOYSA-M tributylplumbyl acetate Chemical compound CCCC[Pb](CCCC)(CCCC)OC(C)=O LMDKALUFKHCRFQ-UHFFFAOYSA-M 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- SOIILYZAUQRZDI-UHFFFAOYSA-L lead(2+) 2,2,2-triphenylacetate Chemical compound [Pb+2].C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)[O-])C1=CC=CC=C1.C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)[O-])C1=CC=CC=C1 SOIILYZAUQRZDI-UHFFFAOYSA-L 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- SBXVIQINPJYMHB-UHFFFAOYSA-N triphenyllead Chemical compound C1=CC=CC=C1[Pb](C=1C=CC=CC=1)C1=CC=CC=C1 SBXVIQINPJYMHB-UHFFFAOYSA-N 0.000 description 3
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 2
- BVGJUOBMHAMGND-UHFFFAOYSA-N 1-(4-ethylmorpholin-4-ium-4-yl)ethanone Chemical compound CC[N+]1(C(C)=O)CCOCC1 BVGJUOBMHAMGND-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 231100000481 chemical toxicant Toxicity 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 239000003440 toxic substance Substances 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- JVKRKMWZYMKVTQ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JVKRKMWZYMKVTQ-UHFFFAOYSA-N 0.000 description 1
- 240000008564 Boehmeria nivea Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- -1 i.e. Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 239000002481 rotproofing Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- KXBADNRYDZGNCW-UHFFFAOYSA-N tributyllead Chemical compound CCCC[Pb](CCCC)CCCC KXBADNRYDZGNCW-UHFFFAOYSA-N 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 210000002268 wool Anatomy 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/50—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with organometallic compounds; with organic compounds containing boron, silicon, selenium or tellurium atoms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2525—Coating or impregnation functions biologically [e.g., insect repellent, antiseptic, insecticide, bactericide, etc.]
Definitions
- This invention relates to a process for producing rotresistant organic fibrous materials and to the products so produced. More specifically, it deals with the application of solutions, or emulsions, of certain organo-lead compounds having the formula R PbY to hydrophilic, organic fibrous materials.
- the resultant treated products have improved resistance to microbiological degradation, are not discolored, and retain their chemical properties. Most important, they have exceptional resistance to physical damage.
- fibrous organic material includes any hydrophilic fibrous material, i.e., organic materials which absorb or adsorb water, such as cotton, viscose rayon, cuprammonium rayon, ramie, jute, wool, paper, paperboard, and the like, including their chemical and/or physical modifications, which may be impregnated with a liquid, and dried. They may be in the form of free fibers, sliver, yarn, thread and woven or nonwoven fabrics. We prefer the use of spun textiles such as threads or woven fabrics.
- rot resistant relates to bactericidal chemicals which when present in the fibrous material are capable of destroying or retarding the action of organisms which normally destroy (rot) hydrophilic organic fibrous materials. Without the aid of such bactericidal chemicals, desized, scoured, and bleached cotton fabrics, or greige goods, are completely destroyed in soil-burial tests in about two to four days. This will be discussed more fully in an example below.
- the fibrous organic materials may be processed by conventional techniques employing conventional equipment.
- the chemical which provides resistance to biological degradation should be one which is easily and simply applied; it should be capable of protecting the fibrous organic material from destructive organisms or be capable of destroying these organisms at low concentrations of the chemical; it must maintain this activity over long periods of time; it must not discolor or physically damage the fibrous material; and it must be compatible with colorants deposited on, and in, the fibrous organic (textile) material for decorative or other purposes, such as waterproofing.
- the process is simple and easily applied. Low concentrations of the organolead compounds serve to completely and quickly destroy or retard the highly active cellulose-destroying organisms and obviate the problem of undesirable color, toxicity, or loss of strength.
- organolead compounds have the formula R PbY Where R is alkyl, aryl, cycloalkyl or combinations of these. Y is an anion including acetate, laurate, imidazole, hydroxide, halogen and the like. These organolead compounds may be prepared by conventional chemical means. Excellent results are obtained when the material is impregnated with 0.5 to 5.0 weight percent of the R PbY solutions and the pickup is 60 to 120 weight percent.
- R PbY compounds N- (tributylplumbyl) imidazole, triphenyllead acetate, triphenyllead laurate, and tributyllead acetate.
- the organolead compound may be dissolved in an aqueous medium such as ethanol or isopropanol to give concentrations ranging from about 1 to 40 weight percent.
- an aqueous medium such as ethanol or isopropanol
- certain nonaqueous solvents such as toluene, mineral spirits, carbon tetrachloride, chloroform and the like are satisfactory solvents.
- the aqueous or nonaqueous lead solutions may be used as such or the nonaqueous solutions of lead may be emulsified to form emulsions.
- These emulsions may be oil-in-water, or water-in-oil types. They may comprise surface active agents, water repellants, resins and colorants.
- the solutions or emulsions may be applied by other conventional methods known to those skilled in the art such as spraying, knife coating, dipping, etc.
- aqueous soluble thickener such as a low viscosity carboxymcthyl cellulose having a viscosity of about 5-20 cps.
- Amounts of thickener ranging from about 1 to 4 weight percent on the total weight of the solution is a good practice.
- the thickener may first be wet with an equal weight of an alkyl alcohol such as ethanol or isopropanol and stirred into the water with a high-speed stirrer to form a uniform mix, after which a small quantity of a cationic surface-active agent such as (N-acetyl- N-ethylmorpholinium ethosulfate) may be added slowly with rapid'stirring.
- a cationic surface-active agent such as (N-acetyl- N-ethylmorpholinium ethosulfate) may be added slowly with rapid'stirring.
- the solution of R PbY is then slowly added with rapid stirring, preferably at a temperature ranging from about 50 to 75 C., and rapidly stirred until a uniform mixture is obtained.
- Impregnating the fibrous material The organic fibrous material is then impregnated with the R PbY solution, by passing the fibrous material into, and through, the R PbY solution.
- the excess organolead solution is then removed by passing the impregnated material through squeeze or padder rolls to remove excess solution. Amounts remaining in the wet fabric may vary from about 60 to 120 percent on the weight of the dry fabric. We prefer about 80 to 100 weight percent pickup, or the proper pickup to give about 0.5 to 5.0 weight percent of the R PbY on the weight of the dry fibrous material.
- the impregnated material is then dried by conventional textile methods.
- the exact temperature range will depend upon the solvent, the presence of thickener, etc., the lower temperature being more suitable for the lower-boiling solvents. If the R PbY is present as a resinous emulsion, higher temperatures from about 130 to 160 C. may be required to cure and fix the resin.
- the textile materials so treated have retained essentially 100% of their strength during the test periods, are not discolored, and their chemical properties remain unchanged.
- the treated organic fibrous materials especially cotton fabrics which are woven or nonwoven, are then buried in soil containing highly active cellulose-destroying organisms and samples removed at various intervals for testing using the AATCC Standard Method 30-1957 T-B-3.
- the following tests were made on desized, scoured, and bleached 54 x 48 cotton fabric. The results follow:
- EXAMPLE 1 Samples of untreated, desized, scoured and bleached 54 x 48 cotton fabric were placed in a rot bed and inspected daily. After two days, the untreated fabric showed signs of deterioration (spots) and after four days had completely disintegrated.
- EXAMPLE 2 A 5% solution of N-(tributylplumbyl) imidazole in ethanol was prepared. Desized, scoured and bleached 54 x 48 printcloth was immersed in the solution and the excess liquid removed by passing the sample through a conventional textile padder with a tight squeeze roll. The fabric was then dried in hot air at 85 C. The treated fabric was then placed in a rot bed. After 56 days of soil burial, the fabric still retained 100% of its original strength.
- EXAMPLE 3 A 2% (2 g.) solution of N-(tributylplumbyl) imidazole in ethanol (98 g.) was prepared. Four grams of low viscosity carboxymethyl cellulose (CMC) was wet with about 2 g. ethanol and then dissolved in 95 g. water using a high-speed magnetic-type stirrer. Two g. of a 35% cationic dispersant (N-acetyl-N-ethyl-morpholinium ethosulfate) was then blended with the CMC solution which was gradually warmed to about 70 C. The N-(tributylplumbyl) imidazole was then stirred slowly into the warm CMC solution.
- CMC carboxymethyl cellulose
- EXAMPLE 4 A 5% ethanol solution of triphenyllead acetate was prepared. Cotton fabric was immersed in this solution and passed through adjustable squeeze rolls to remove excess liquid. Without drying this process was repeated and the fabric was then air dried at C. The fabric retained 100% of its original strength after 42 days of soil burial.
- EXAMPLE 6 5. grams of triphenyllead laurate solution were dissolved in grams of chloroform. Cotton fabrics were padded with the above solution as in Example 2. The fabric retained of its original strength after 42 days of soil burial.
- Cotton fabric was treated with 0.5% N-(tributylplumbyl) imidazole as in Example 5. The fabric, after treatment, was leached for 24 hours (see AATCC Method 30-1957 T-C-l) then tested for rot resistance by the soil burial method. The fabric still retained 100% of its original strength after 28 days.
- EXAMPLE 8 2 grams of tributyllead acetate was dissolved in 17 g. isopropanol. 2 g. CMC and 2 g. of the cationic dispersant of Example 3 were dissolved in 180 ml. water by the procedure of Example 3, after which the tributyllead acetate was added to the warm (70 C.) CMC solution. Sufficient water was then stirred into the tributyllead acetate-CMC solution to give a total of 200 g.
- Cotton fabric was then padded with this solution and dried by the procedure of Example 3. The treated fabric retained essentially 100% of its original strength after 28 days of soil burial.
- a process for rendering organic fibrous materials rot-resistant comprising the steps:
- organolead compound is at least one member of the group consisting of N-(tri'butylplumbyl) imidazole, triphenyllead acetate, and tributyllead acetate.
- aqueous solution comprising the organolead compound also contains a thickener and a surfactant.
- aqueous solution comprises from about 8 to 50 percent ethanol, 0.5 to 5.0 percent organolead compound, 45 to 90 percent Water, 1.0 to 2.0 percent low viscosity carboxymethyl cellulose, and 1 percent cationic surfactant, all percentages by weight.
- a process for rendering organic fibrous materials rot-resistant comprising the steps:
- nonaqueous solvent is selected from the group consisting of chloroform, pentane, hexane, and heptane and the organolead compound is triphenyllead laurate.
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Paper (AREA)
Description
United States Patent 3,420,701 PROCESS FOR IMPARTING ROT-RESISTANCE TO AN ORGANIC TEXTILE MATERIAL AND THE RESULTING MATERIAL Darrell J. Donaldson and Wilma A. Guice, New Orleans, and George L. Drake, .Ir., and Wilson A. Reeves, Metairie, La., assignors to the United States of America as represented by the Secretary of Agriculture No Drawing. Filed Apr. 29, 1966, Ser. No. 546,182 U.S. Cl. 117-1385 Claims Int. Cl. D06m 13/50 A non-exclusive, irrevocable, royalty-free license in the invention herein described, throughout the world for all purposes of the United States Government, with the power to grant sublicenses for such purposes, is hereby granted to the Government of the United States of America.
This invention relates to a process for producing rotresistant organic fibrous materials and to the products so produced. More specifically, it deals with the application of solutions, or emulsions, of certain organo-lead compounds having the formula R PbY to hydrophilic, organic fibrous materials. The resultant treated products have improved resistance to microbiological degradation, are not discolored, and retain their chemical properties. Most important, they have exceptional resistance to physical damage.
The process which is the subject of this invention is a separate and distinct embodiment of the process disclosed in our application, Ser. No. 546,169, filed of even date.
The term fibrous organic material, as used herein, includes any hydrophilic fibrous material, i.e., organic materials which absorb or adsorb water, such as cotton, viscose rayon, cuprammonium rayon, ramie, jute, wool, paper, paperboard, and the like, including their chemical and/or physical modifications, which may be impregnated with a liquid, and dried. They may be in the form of free fibers, sliver, yarn, thread and woven or nonwoven fabrics. We prefer the use of spun textiles such as threads or woven fabrics.
The term rot resistant relates to bactericidal chemicals which when present in the fibrous material are capable of destroying or retarding the action of organisms which normally destroy (rot) hydrophilic organic fibrous materials. Without the aid of such bactericidal chemicals, desized, scoured, and bleached cotton fabrics, or greige goods, are completely destroyed in soil-burial tests in about two to four days. This will be discussed more fully in an example below.
It is an advantage of the process of this invention that the fibrous organic materials may be processed by conventional techniques employing conventional equipment.
Heretofore, the protection of fibrous organic (textile) materials from attack by bacterial organisms has posed serious problems for the textile industry, and particularly when dealing with the manufacture of textiles for outdoor use where they may be alternately exposed to rain, cloudy weather and the heat of a hot sun; or for cotton canvas, one side of which is in contact with the ground.
Ideally, the chemical which provides resistance to biological degradation should be one which is easily and simply applied; it should be capable of protecting the fibrous organic material from destructive organisms or be capable of destroying these organisms at low concentrations of the chemical; it must maintain this activity over long periods of time; it must not discolor or physically damage the fibrous material; and it must be compatible with colorants deposited on, and in, the fibrous organic (textile) material for decorative or other purposes, such as waterproofing.
3,420,701 Patented Jan. 7, 1969 ice It has been known to treat fibrous materials to render them rot resistant. Toxic chemicals such as mercury compounds have been used but fibrous materials containing toxic chemicals may be dangerous to humans and animals. Deposition of bactericidal chemicals on fibrous materials frequently produces discoloration or tendering of the substrate. Many chemicals are expensive while others require large amounts of the rot-proofing chemical and accordingly also are expensive. Thus, it is seen that there is a real need in the textile industry for an effective method of destroying rot-producing organisms unattended by the above-described disadvantages.
We have now found that by impregnating organic fibrous materials with solutions of certain organolead compounds, it is possible to destroy or retard the highly active, cellulose-destroying organism thereby rendering these materials rot-resistant in a remarkably efiicient and simple manner.
In general terms, the process of our invention may be described as follows:
1) Prepare an aqueous solution or emulsion of the organolead compound.
(2) Impregnate the organic fibrous material with the lead solution.
(3) Remove the excess organolead solution by passing the organo fibrous material through a pair of squeeze rolls (padder rolls) adjusted to retain about 60 to weight percent of the solution on the dry weight of the fabric.
(4) Dry the impregnated fibrous material.
The process is simple and easily applied. Low concentrations of the organolead compounds serve to completely and quickly destroy or retard the highly active cellulose-destroying organisms and obviate the problem of undesirable color, toxicity, or loss of strength.
Preparation of organolead solutions The organolead compounds have the formula R PbY Where R is alkyl, aryl, cycloalkyl or combinations of these. Y is an anion including acetate, laurate, imidazole, hydroxide, halogen and the like. These organolead compounds may be prepared by conventional chemical means. Excellent results are obtained when the material is impregnated with 0.5 to 5.0 weight percent of the R PbY solutions and the pickup is 60 to 120 weight percent.
Examples of the preferred R PbY compounds are N- (tributylplumbyl) imidazole, triphenyllead acetate, triphenyllead laurate, and tributyllead acetate.
The organolead compound may be dissolved in an aqueous medium such as ethanol or isopropanol to give concentrations ranging from about 1 to 40 weight percent. However, as the length of the carbon chain in the anion increases, certain nonaqueous solvents such as toluene, mineral spirits, carbon tetrachloride, chloroform and the like are satisfactory solvents. The aqueous or nonaqueous lead solutions may be used as such or the nonaqueous solutions of lead may be emulsified to form emulsions. These emulsions may be oil-in-water, or water-in-oil types. They may comprise surface active agents, water repellants, resins and colorants. The solutions or emulsions may be applied by other conventional methods known to those skilled in the art such as spraying, knife coating, dipping, etc.
It is within the scope of our invention to add a minor portion of an aqueous soluble thickener such as a low viscosity carboxymcthyl cellulose having a viscosity of about 5-20 cps. to the aqueous solution of the organolead compound. Amounts of thickener ranging from about 1 to 4 weight percent on the total weight of the solution is a good practice. The thickener may first be wet with an equal weight of an alkyl alcohol such as ethanol or isopropanol and stirred into the water with a high-speed stirrer to form a uniform mix, after which a small quantity of a cationic surface-active agent such as (N-acetyl- N-ethylmorpholinium ethosulfate) may be added slowly with rapid'stirring. The solution of R PbY is then slowly added with rapid stirring, preferably at a temperature ranging from about 50 to 75 C., and rapidly stirred until a uniform mixture is obtained.
Impregnating the fibrous material The organic fibrous material is then impregnated with the R PbY solution, by passing the fibrous material into, and through, the R PbY solution. The excess organolead solution is then removed by passing the impregnated material through squeeze or padder rolls to remove excess solution. Amounts remaining in the wet fabric may vary from about 60 to 120 percent on the weight of the dry fabric. We prefer about 80 to 100 weight percent pickup, or the proper pickup to give about 0.5 to 5.0 weight percent of the R PbY on the weight of the dry fibrous material.
Drying the impregnated fibrous material The impregnated material is then dried by conventional textile methods. We prefer hot air at a temperature of about 60130 C., preferably about 75 to 90 C. The exact temperature range will depend upon the solvent, the presence of thickener, etc., the lower temperature being more suitable for the lower-boiling solvents. If the R PbY is present as a resinous emulsion, higher temperatures from about 130 to 160 C. may be required to cure and fix the resin.
The textile materials so treated have retained essentially 100% of their strength during the test periods, are not discolored, and their chemical properties remain unchanged.
The treated organic fibrous materials, especially cotton fabrics which are woven or nonwoven, are then buried in soil containing highly active cellulose-destroying organisms and samples removed at various intervals for testing using the AATCC Standard Method 30-1957 T-B-3. The following tests were made on desized, scoured, and bleached 54 x 48 cotton fabric. The results follow:
EXAMPLE 1 Samples of untreated, desized, scoured and bleached 54 x 48 cotton fabric were placed in a rot bed and inspected daily. After two days, the untreated fabric showed signs of deterioration (spots) and after four days had completely disintegrated.
EXAMPLE 2 A 5% solution of N-(tributylplumbyl) imidazole in ethanol was prepared. Desized, scoured and bleached 54 x 48 printcloth was immersed in the solution and the excess liquid removed by passing the sample through a conventional textile padder with a tight squeeze roll. The fabric was then dried in hot air at 85 C. The treated fabric was then placed in a rot bed. After 56 days of soil burial, the fabric still retained 100% of its original strength.
EXAMPLE 3 A 2% (2 g.) solution of N-(tributylplumbyl) imidazole in ethanol (98 g.) was prepared. Four grams of low viscosity carboxymethyl cellulose (CMC) was wet with about 2 g. ethanol and then dissolved in 95 g. water using a high-speed magnetic-type stirrer. Two g. of a 35% cationic dispersant (N-acetyl-N-ethyl-morpholinium ethosulfate) was then blended with the CMC solution which was gradually warmed to about 70 C. The N-(tributylplumbyl) imidazole was then stirred slowly into the warm CMC solution.
Desized, scoured and bleached 54 x 48 cotton printcloth was then impregnated with this solution, the excess removed by passage through squeeze rolls and the fabric dried in hot air at an air temperature of about 150 C. The treated fabric retained all its strength (100%) after 70 days of soil burial.
EXAMPLE 4 A 5% ethanol solution of triphenyllead acetate was prepared. Cotton fabric was immersed in this solution and passed through adjustable squeeze rolls to remove excess liquid. Without drying this process was repeated and the fabric was then air dried at C. The fabric retained 100% of its original strength after 42 days of soil burial.
EXAMPLE 5 Cotton samples were padded with a 0.5% ethanolic solution of N-(tributylplumbyl) imidazole in a similar manner as described in Example 2. The fabric retained 100% of its original strength after 28 days of soil burial.
EXAMPLE 6 5. grams of triphenyllead laurate solution were dissolved in grams of chloroform. Cotton fabrics were padded with the above solution as in Example 2. The fabric retained of its original strength after 42 days of soil burial.
EXAMPLE 7 Cotton fabric was treated with 0.5% N-(tributylplumbyl) imidazole as in Example 5. The fabric, after treatment, was leached for 24 hours (see AATCC Method 30-1957 T-C-l) then tested for rot resistance by the soil burial method. The fabric still retained 100% of its original strength after 28 days.
EXAMPLE 8 2 grams of tributyllead acetate was dissolved in 17 g. isopropanol. 2 g. CMC and 2 g. of the cationic dispersant of Example 3 were dissolved in 180 ml. water by the procedure of Example 3, after which the tributyllead acetate was added to the warm (70 C.) CMC solution. Sufficient water was then stirred into the tributyllead acetate-CMC solution to give a total of 200 g.
Cotton fabric was then padded with this solution and dried by the procedure of Example 3. The treated fabric retained essentially 100% of its original strength after 28 days of soil burial.
It should be noted that in all the eight examples above, the treated fabrics did not lose strength during soil burial tests, and one of them (Example 3) after 70 days. These results were unexpected.
We claim:
1. A process for rendering organic fibrous materials rot-resistant comprising the steps:
(a) preparing an aqueous solution comprising 0.5 to about 5.0 weight percent of an organolead compound having the formula R PbY where R is at least one member of the group consisting of alkyl, aryl, and cycloalkyl, and Y is an anion selected from the group consisting of acetate, imidazole, hydroxide and halogen;
(b) impregnating the organic fibrous material with the organolead solution;
(c) removing the excess organolead (R PbY) solution by passing the impregnated organic fibrous material through a pair of squeeze rolls adjusted to retain from about 60 to weight percent of the solution on the dry weight of the fibrous material; and
(d) drying the impregnated fibrous organic material.
2. The process defined in claim 1 wherein the organic fibrous material is a cellulosic fibrous material.
3. The product resulting from the process of claim 2.
4. The process defined in claim 1 wherein the organolead compound is at least one member of the group consisting of N-(tri'butylplumbyl) imidazole, triphenyllead acetate, and tributyllead acetate.
5. The process defined in claim 1 wherein the aqueous solution comprising the organolead compound also contains a thickener and a surfactant.
6. The product resulting from the process of claim 5.
7. The process defined in claim 5 wherein the aqueous solution comprises from about 8 to 50 percent ethanol, 0.5 to 5.0 percent organolead compound, 45 to 90 percent Water, 1.0 to 2.0 percent low viscosity carboxymethyl cellulose, and 1 percent cationic surfactant, all percentages by weight.
8. A process for rendering organic fibrous materials rot-resistant comprising the steps:
(a) preparing a nonaqueous solution comprising 0.5 to about 5.0 weight percent of an organolead compound where R is at least one member of the group consisting of alkyl, aryl and cycloalkyl, and Y is an aliphatic radical having 12 to 20 carbon atoms;
(b) impregnating the organic fibrous material with the organolead solution;
(c) removing the excess organolead solution by passing the impregnated organic fibrous material through a pair of squeeze rolls adjusted to retain from about 60 to 120 weight percent of the solution on the dry weight of the fibrous material; and
(d) drying the impregnated fibrous organic material.
9. The product resulting from the process of claim 8.
10. The process defined in claim 8 wherein the nonaqueous solvent is selected from the group consisting of chloroform, pentane, hexane, and heptane and the organolead compound is triphenyllead laurate.
References Cited UNITED STATES PATENTS 2,763,574 9/1956 Ruperti 117-1385 2,938,815 5/1960 Van Bochove et al. 117-143 X 3,119,715 1/1964 Reeves et al. 117-138.5 3,142,614 7/1964 Ligett 167-22 3,183,118 5/1965 Conner 117-1385 3,183,149 5/1965 Gonzales et a1. 117-143 X 3,317,345 5/1967 Fluck et a1 117-1385 WILLIAM D. MARTIN, Primary Examiner.
THEODORE G. DAVIS, Assistant Examiner.
US. Cl. X.R.
Claims (1)
1. A PROCESS FOR RENDERING ORGANIC FIBROUS MATERIALS ROT-RESISTANT COMPRISING THE STEPS: (A) PREPARING AN AQUEOUS SOLUTION COMPRISING 0.5 TO ABOUT 5.0 WEIGHT PERCENT OF AN ORGANOLEAD COMPOUND HAVING THE FORMULA R3PBY WHERE R IS AT LEAST ONE MEMBER OF THE GROUP CONSISTING OF ALKYL, ARYL, AND CYCLOALKYL, AND Y IS AN ANION SELECTED FROM THE GROUP CONSISTNG OF ACETATE, IMIDAZOLE, HYDROXIDE AND HALOGEN; (D) IMPREGNATING THE ORGANIC FIBROUS MATERIAL WITH THE ORGANOLEAD SOLUTION; (C) REMOVING THE EXCESS ORGANOLEAD (R3PBY) SOLUTION BY PASSING THE IMPREGNATED ORGANIC FIBROUS MATERIAL THROUGH A PAIR OF SQUEEZE ROLLS ADJUSTED TO RETAIN FROM ABOUT 60 120 WEIGHT PERCENT OF THE SOLUTION ON THE DRY WEIGHT OF THE FIBROUS MATERIAL; AND (D) DRYING THE IMPREGNATED FIBROUS ORGANIC MATERIAL.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54616966A | 1966-04-29 | 1966-04-29 | |
| US54618266A | 1966-04-29 | 1966-04-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3420701A true US3420701A (en) | 1969-01-07 |
Family
ID=27068136
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US3420701D Expired - Lifetime US3420701A (en) | 1966-04-29 | 1966-04-29 | Process for imparting rot-resistance to an organic textile material and the resulting material |
| US3420700D Expired - Lifetime US3420700A (en) | 1966-04-29 | 1966-04-29 | Process for imparting rot-resistance to an organic textile material and the resulting material |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US3420700D Expired - Lifetime US3420700A (en) | 1966-04-29 | 1966-04-29 | Process for imparting rot-resistance to an organic textile material and the resulting material |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US3420701A (en) |
| BE (2) | BE697815A (en) |
| DE (2) | DE1619100A1 (en) |
| GB (2) | GB1129900A (en) |
| NL (2) | NL6705636A (en) |
| SE (2) | SE349071B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20170007972A1 (en) * | 2007-02-08 | 2017-01-12 | Linsheng Walter Tien | Magnetic Stirring Device and Method of Using the Same |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2763574A (en) * | 1951-07-10 | 1956-09-18 | Ciba Ltd | Method for protection of cellulosic fibrous material from attack by micro-organisms |
| US2938815A (en) * | 1957-07-04 | 1960-05-31 | Tno | Process for making cellulose materials rotproof |
| US3119715A (en) * | 1962-04-06 | 1964-01-28 | Wilson A Reeves | Processes for treating cellulosic textiles with acid colloids of methylolmelamine |
| US3142614A (en) * | 1961-07-10 | 1964-07-28 | Ethyl Corp | Polyvalent organo-lead fungicide |
| US3183149A (en) * | 1962-09-20 | 1965-05-11 | Elwood J Gonzales | Process for making cellulosic textiles rot resistant with zirconium salts and phenols |
| US3183118A (en) * | 1963-01-22 | 1965-05-11 | Charles J Conner | Reaction products of nickel, copper and mercury salts and process for rendering cotton fabric rot resistant therewith |
| US3317345A (en) * | 1963-06-25 | 1967-05-02 | American Cyanamid Co | Rot-resistant finish for textile materials |
-
1966
- 1966-04-29 US US3420701D patent/US3420701A/en not_active Expired - Lifetime
- 1966-04-29 US US3420700D patent/US3420700A/en not_active Expired - Lifetime
-
1967
- 1967-04-18 DE DE19671619100 patent/DE1619100A1/en active Pending
- 1967-04-18 DE DE19671619101 patent/DE1619101A1/en active Pending
- 1967-04-21 NL NL6705636A patent/NL6705636A/xx unknown
- 1967-04-21 NL NL6705635A patent/NL6705635A/xx unknown
- 1967-04-27 GB GB1946467A patent/GB1129900A/en not_active Expired
- 1967-04-27 GB GB1946367A patent/GB1129899A/en not_active Expired
- 1967-04-27 SE SE598667A patent/SE349071B/xx unknown
- 1967-04-27 SE SE598567A patent/SE349070B/xx unknown
- 1967-04-28 BE BE697815D patent/BE697815A/xx unknown
- 1967-04-28 BE BE697816D patent/BE697816A/xx unknown
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2763574A (en) * | 1951-07-10 | 1956-09-18 | Ciba Ltd | Method for protection of cellulosic fibrous material from attack by micro-organisms |
| US2938815A (en) * | 1957-07-04 | 1960-05-31 | Tno | Process for making cellulose materials rotproof |
| US3142614A (en) * | 1961-07-10 | 1964-07-28 | Ethyl Corp | Polyvalent organo-lead fungicide |
| US3119715A (en) * | 1962-04-06 | 1964-01-28 | Wilson A Reeves | Processes for treating cellulosic textiles with acid colloids of methylolmelamine |
| US3183149A (en) * | 1962-09-20 | 1965-05-11 | Elwood J Gonzales | Process for making cellulosic textiles rot resistant with zirconium salts and phenols |
| US3183118A (en) * | 1963-01-22 | 1965-05-11 | Charles J Conner | Reaction products of nickel, copper and mercury salts and process for rendering cotton fabric rot resistant therewith |
| US3317345A (en) * | 1963-06-25 | 1967-05-02 | American Cyanamid Co | Rot-resistant finish for textile materials |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20170007972A1 (en) * | 2007-02-08 | 2017-01-12 | Linsheng Walter Tien | Magnetic Stirring Device and Method of Using the Same |
Also Published As
| Publication number | Publication date |
|---|---|
| US3420700A (en) | 1969-01-07 |
| SE349070B (en) | 1972-09-18 |
| NL6705635A (en) | 1967-10-30 |
| GB1129900A (en) | 1968-10-09 |
| GB1129899A (en) | 1968-10-09 |
| DE1619101A1 (en) | 1969-10-23 |
| SE349071B (en) | 1972-09-18 |
| BE697816A (en) | 1967-10-02 |
| NL6705636A (en) | 1967-10-30 |
| DE1619100A1 (en) | 1970-12-03 |
| BE697815A (en) | 1967-10-02 |
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