US20040006827A1 - Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates - Google Patents
Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates Download PDFInfo
- Publication number
- US20040006827A1 US20040006827A1 US10/611,746 US61174603A US2004006827A1 US 20040006827 A1 US20040006827 A1 US 20040006827A1 US 61174603 A US61174603 A US 61174603A US 2004006827 A1 US2004006827 A1 US 2004006827A1
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- Prior art keywords
- npb
- substrates
- set forth
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- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 47
- 239000000203 mixture Substances 0.000 title claims abstract description 27
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 title claims abstract description 20
- 239000000126 substance Substances 0.000 title claims abstract description 18
- 238000000034 method Methods 0.000 title claims abstract description 16
- 239000008365 aqueous carrier Substances 0.000 title claims abstract description 5
- 238000009472 formulation Methods 0.000 title claims abstract description 4
- 238000011282 treatment Methods 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 7
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 238000005187 foaming Methods 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims 1
- 230000000844 anti-bacterial effect Effects 0.000 claims 1
- 239000003125 aqueous solvent Substances 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 238000009991 scouring Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 7
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract description 4
- 230000007613 environmental effect Effects 0.000 abstract description 3
- 239000000969 carrier Substances 0.000 abstract description 2
- 238000005516 engineering process Methods 0.000 abstract description 2
- 239000004753 textile Substances 0.000 description 15
- 238000012360 testing method Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 10
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000006260 foam Substances 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 229920000058 polyacrylate Polymers 0.000 description 6
- 229920000297 Rayon Polymers 0.000 description 5
- 239000002964 rayon Substances 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004088 foaming agent Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 101100352919 Caenorhabditis elegans ppm-2 gene Proteins 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000004758 synthetic textile Substances 0.000 description 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- WBHAUHHMPXBZCQ-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound COC1=CC=CC(C)=C1O WBHAUHHMPXBZCQ-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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004855 creaseproofing Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical class FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- YCOZIPAWZNQLMR-UHFFFAOYSA-N heptane - octane Natural products CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 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
- 229940094933 n-dodecane Drugs 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004634 thermosetting polymer Substances 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
- D06M13/08—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with halogenated hydrocarbons
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B9/00—Solvent-treatment of textile materials
- D06B9/06—Solvent-treatment of textile materials with recovery of the solvent
-
- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
- D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
- D06M2200/11—Oleophobic properties
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
- Y02P70/62—Manufacturing or production processes characterised by the final manufactured product related technologies for production or treatment of textile or flexible materials or products thereof, including footwear
Definitions
- NPB n-propyl bromide
- NPB has shown an excellent alternative to current aqueous and chlorinated hydrocarbons as a carrier medium for application of organics to substrates.
- NPB is non-regulated, non-toxic and has no ozone pollution properties.
- NPB is economical and environmentally friendly.
- NPB NPB
- the invention relates to methods and formulations to provide substrates with treatment to include oil and water repellant treatment, for example; the treatment of home textiles and apparel, which achieve desired effects with significantly smaller amounts of expensive fluorocarbon compounds as Compared to available current technology, as illustrated in Example 2 Compared to Example 4.
- compositions according to the invention should furthermore impart to the substrates, in particular the home textiles, water-repellant actions that meet increased requirements.
- Another object comprises providing treatment compositions with which the heat treatment can be carried out at the lowest temperature or, preferably, no heat treatment is necessary (Example 3).
- invention relates to substrates from the group consisting of naturally occurring and synthetic textiles and their mixtures, leather, mineral substances, thermoplastic and thermosetting polymers and paper, which are treated with fluorine-containing compositions of the type mentioned below in an amount of 10 to 10,000 ppm, preferably 50 to 5,000 ppm, particularly preferably 100 to 2,000 ppm, calculated as fluorine and based on the total weight of substrates provided with an oil-, water- and soil-repellant treatment.
- textile auxiliary chemicals can be added during preparation of the treatment formula as according to the invention, or subsequently.
- additives are crease-proofing and soft handle agents, melamine, flame retardant, oleophobizing agents, hydrophobizing agents, Urethane, finishing agents, extenders for textile auxiliaries and others.
- Substrates which are suitable for imparting oil-, water- and soil-repellant properties according to the invention are: linen, cotton, wool, silk, jute, polyamide, polyester, polyacrylonitrile and mixtures thereof, leather, stone slabs, floor tiles, glazed tiles, roof tiles, glass, ground surfaces of silicon, foils and films and compact workpieces of polyolefins, polyesters, polyamides, polycarbonates, polyurethane, polyacetals, polyethers, polysulphides, polysulphones, polyamides and other thermoplastics, as well as of phenol/formaldehyde resins, urea/formaldehyde resins, melamine/formaldehyde resins and other thermosetting resins, paper and paper-like materials, such as paperboard.
- Preferred base substrates are home textiles based on naturally occurring and synthetic textiles and their mixtures, which are employed, for example, as carpets, curtains, decorative materials or coverings for upholstered furniture.
- Processes for the treatment of such base substrates and therefore for application of the fluorine-containing compositions according to the invention are known to the expert and are, for example, foaming, dipping or spraying of the base substrates; the compositions according to the invention furthermore can be employed during the production of the base substrates, for example the pulp.
- Textiles as base substrates preferably home textiles and apparel can be treated, for example, in the padding, spraying or foaming process.
- the padder consists of a liquor trough (chassis) and at least one pair of rubber rolls (Example 2).
- the textiles to be treated are impregnated with the treatment liquor in the chassis and squeezed off between the rolls; the liquor runs back into the chassis. It is very important that a uniform liquor pick-up is achieved over the entire width of the goods during squeezing-off.
- the liquor pick-up is stated in percentage of the weight of goods, and for normal textile constructions can be between 30 and 300%, depending on the quality of the goods and the padder pressure used.
- Example 3 the textile is sprayed with the treatment liquor.
- the treatment liquor is finely divided by nozzles and applied uniformly.
- An amount of treatment liquor precisely defined beforehand is applied to one square meter of textile goods.
- the treatment liquor is continuously foamed mechanically in a commercially available mixer with out the addition of a foaming agent.
- the foam is produced in the mixing head by mixing the liquor with air.
- the foam, which emerges, is conveyed via a foam line to a discharge slot in the applicator.
- the goods are pressed against the slot and taken off via a separate unit, for example a stenter frame.
- a concentration of 98% NPB and 2% Perfluoroalkyl polyacrylate were used.
- the experiments were carried out on the Gaston Systems, Inc. Foam Applicator, Stanly, N.C.
- this invention involves the surprising discovery that the use of NPB applied in 100% concentration via dipping and squeezing with pressure rollers (Padding) and the NPB being evaporated away imparts a much improved softness and luster to textile substrates, especially home furnishing, apparel fabrics and upholstery fabrics.
- the textiles preferably home textiles
- the textiles are dried, it being possible to use temperatures of 120.degree. to 170.degree. C. to achieve the desired treatment effect according to the known procedure.
- temperatures 120.degree. to 170.degree. C.
- good oil-, water- and soil-repellant treatments can also be obtained with the new compositions according to the invention at significantly lower drying temperatures, for example at 25.degree. C. (Example 3).
- Oil-repellency accordinging to AATCC 118-1972: The test sample is placed on a horizontal, smooth surface, a small drop (drop diameter about 5 mm) of he test liquids is applied to the test sample with the aid of a dropping pipette, In addition, the sample is evaluated as specified.
- the AATCC oil-repellency level of a test fabric is the highest number of that test liquid which does not wet or penetrate into the test material within a time span of 30 seconds.
- the test liquids and mixtures for the test method are: No. 1: Nujol or paraffin oil DAB 8; No. 2: 65% by volume of Nujol and 35% by volume of n-hexadecane; No. 3: n-hexadecane; No. 4: n-tetradecane; No. 5: n-dodecane; No. 6: n-decane; No. 7: n-octane; No. 8: n-heptane.
- Repellency towards a water/alcohol mixture (hydrophobicity): Drops of water/isopropanol mixtures (ratio 90/10 to 10/90) are applied to the test sample.
- the test result corresponds to the mixture with the highest isopropanol content which remains on the test sample in unchanged form for at least 20 seconds (the value 80/20, for example, is better than 20/80).
- compositions which are not according to the invention (Example 4) and which represent the prior art are the following: Nuva HPU (Clariant Corporation). Scotchgard.RTM. FC 396 (3M Comp.) according to DE-A 2 149 292 Baygard.RTM. SF-A. (Bayer AG) according to DE-A 3 307 420 and Zonyl (E. I. Dupont)
- compositions according to the invention are non-aqueous solutions contents of which comprise a mixture of NPB (component A) and one or more poly (meth) acrylates (component B).
- the substrates used were (1) White Polyester 8 oz/sq yd (PES), (2) 100% Cotton interlock and (3) 60/40 PES and Rayon Blend.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
The present invention relates to methods and chemical formulations utilizing NPB(n-propyl bromide) also called 1-bromopropane or propyl bromide or 1-BP or N-Bromopropane as non-aqueous carrier mediums to apply fluorocarbons and other chemicals to substrates, whereby the NPB is evaporated away leaving the remaining chemicals on the substrate. The present invention offers formula and method for applying organic chemicals to substrates that perform superior to current water based technology. Additional, the invention offers a more economical and environmental friendly alternative to current chlorinated hydrocarbons carriers that are being phased out by mandate of the Environmental Protection Agency (EPA).
Description
- NPB (n-propyl bromide) has been used in the metal parts degreasing industry, particularly in vapor degreasers for years. Now according to the invention it has been discovered to have a very useful and desired purpose in other industries. Many substrates, for example, home textiles, carpets, upholstery acquire oil-,water- and soil-repellant properties by treatment with fluorocarbons.
- These chemicals are now applied to substrates with water based (aqueous) carriers requiring other auxiliary chemicals i.e.: emulsifiers and dispersing agents to keep organics in suspension. These auxiliary chemicals needed for aqueous application often lesson the intended benefit of the applied chemical to the substrate. These aqueous carriers require high temperatures and expensive drying systems to evaporate the water. Chlorinated hydrocarbons have been used in the past as carrier mediums to apply organic chemicals to substrates when an aqueous carrier could not be used. Chlorinated hydrocarbons are being phased out by mandate of the Environmental Protection Agency (EPA).
- By this invention, NPB has shown an excellent alternative to current aqueous and chlorinated hydrocarbons as a carrier medium for application of organics to substrates. NPB is non-regulated, non-toxic and has no ozone pollution properties. NPB is economical and environmentally friendly.
- After extensive study, it has been found that the use of NPB as a carrier dramatically improves the performances and durability of benefits achieved by application of organics to substrate and that this invention is superior to current methods and chemistry.
- The invention relates to methods and formulations to provide substrates with treatment to include oil and water repellant treatment, for example; the treatment of home textiles and apparel, which achieve desired effects with significantly smaller amounts of expensive fluorocarbon compounds as Compared to available current technology, as illustrated in Example 2 Compared to Example 4.
- The following description, taken in conjunction with the referenced examples, is presented to enable one of ordinary skill in the art to make and use the invention. Various modifications will be readily apparent to those Skilled in the art, and the general principles defined herein may be applied to a wide range of aspects. Thus, the present invention is not intended to be limited to the aspects presented, but is to be accorded the widest scope consistent with the principles and novel features disclosed herein. Furthermore, the compositions according to the invention should furthermore impart to the substrates, in particular the home textiles, water-repellant actions that meet increased requirements. Another object comprises providing treatment compositions with which the heat treatment can be carried out at the lowest temperature or, preferably, no heat treatment is necessary (Example 3).
- In one aspect, invention relates to substrates from the group consisting of naturally occurring and synthetic textiles and their mixtures, leather, mineral substances, thermoplastic and thermosetting polymers and paper, which are treated with fluorine-containing compositions of the type mentioned below in an amount of 10 to 10,000 ppm, preferably 50 to 5,000 ppm, particularly preferably 100 to 2,000 ppm, calculated as fluorine and based on the total weight of substrates provided with an oil-, water- and soil-repellant treatment.
- In another aspect, other textile auxiliary chemicals can be added during preparation of the treatment formula as according to the invention, or subsequently. Such additives are crease-proofing and soft handle agents, melamine, flame retardant, oleophobizing agents, hydrophobizing agents, Urethane, finishing agents, extenders for textile auxiliaries and others.
- Substrates which are suitable for imparting oil-, water- and soil-repellant properties according to the invention are: linen, cotton, wool, silk, jute, polyamide, polyester, polyacrylonitrile and mixtures thereof, leather, stone slabs, floor tiles, glazed tiles, roof tiles, glass, ground surfaces of silicon, foils and films and compact workpieces of polyolefins, polyesters, polyamides, polycarbonates, polyurethane, polyacetals, polyethers, polysulphides, polysulphones, polyamides and other thermoplastics, as well as of phenol/formaldehyde resins, urea/formaldehyde resins, melamine/formaldehyde resins and other thermosetting resins, paper and paper-like materials, such as paperboard. Preferred base substrates are home textiles based on naturally occurring and synthetic textiles and their mixtures, which are employed, for example, as carpets, curtains, decorative materials or coverings for upholstered furniture.
- Processes for the treatment of such base substrates and therefore for application of the fluorine-containing compositions according to the invention are known to the expert and are, for example, foaming, dipping or spraying of the base substrates; the compositions according to the invention furthermore can be employed during the production of the base substrates, for example the pulp.
- Textiles as base substrates, preferably home textiles and apparel can be treated, for example, in the padding, spraying or foaming process. The padder consists of a liquor trough (chassis) and at least one pair of rubber rolls (Example 2). The textiles to be treated are impregnated with the treatment liquor in the chassis and squeezed off between the rolls; the liquor runs back into the chassis. It is very important that a uniform liquor pick-up is achieved over the entire width of the goods during squeezing-off.
- In the padding process, the liquor pick-up is stated in percentage of the weight of goods, and for normal textile constructions can be between 30 and 300%, depending on the quality of the goods and the padder pressure used.
- In the spraying process, (Example 3) the textile is sprayed with the treatment liquor. The treatment liquor is finely divided by nozzles and applied uniformly. An amount of treatment liquor precisely defined beforehand is applied to one square meter of textile goods.
- In the foaming process, the treatment liquor is continuously foamed mechanically in a commercially available mixer with out the addition of a foaming agent. The foam is produced in the mixing head by mixing the liquor with air. The foam, which emerges, is conveyed via a foam line to a discharge slot in the applicator. The goods are pressed against the slot and taken off via a separate unit, for example a stenter frame. In example 1, a concentration of 98% NPB and 2% Perfluoroalkyl polyacrylate were used. The experiments were carried out on the Gaston Systems, Inc. Foam Applicator, Stanly, N.C.
- By the invention, it has been discovered surprisingly that a mixture of NPB and Perfluoroalkyl polyacrylate can be foamed with or without the aid of a foaming agent (Example 1). Not using foaming agents greatly improves the benefit of the applied fluorine composition to the substrate and reduces the amount of compound added to fabric to achieve water and oil repellency.
- In another aspect, this invention involves the surprising discovery that the use of NPB applied in 100% concentration via dipping and squeezing with pressure rollers (Padding) and the NPB being evaporated away imparts a much improved softness and luster to textile substrates, especially home furnishing, apparel fabrics and upholstery fabrics.
- After the treatment, the textiles, preferably home textiles, are dried, it being possible to use temperatures of 120.degree. to 170.degree. C. to achieve the desired treatment effect according to the known procedure. However, good oil-, water- and soil-repellant treatments can also be obtained with the new compositions according to the invention at significantly lower drying temperatures, for example at 25.degree. C. (Example 3).
- Samples of the materials thus pretreated were taken for testing of the following effects:
- Oil-repellency (according to AATCC 118-1972): The test sample is placed on a horizontal, smooth surface, a small drop (drop diameter about 5 mm) of he test liquids is applied to the test sample with the aid of a dropping pipette, In addition, the sample is evaluated as specified.
- The AATCC oil-repellency level of a test fabric is the highest number of that test liquid which does not wet or penetrate into the test material within a time span of 30 seconds. The test liquids and mixtures for the test method are: No. 1: Nujol or paraffin oil DAB 8; No. 2: 65% by volume of Nujol and 35% by volume of n-hexadecane; No. 3: n-hexadecane; No. 4: n-tetradecane; No. 5: n-dodecane; No. 6: n-decane; No. 7: n-octane; No. 8: n-heptane.
- Repellency towards a water/alcohol mixture (hydrophobicity): Drops of water/isopropanol mixtures (ratio 90/10 to 10/90) are applied to the test sample. The test result corresponds to the mixture with the highest isopropanol content which remains on the test sample in unchanged form for at least 20 seconds (the value 80/20, for example, is better than 20/80).
- Compositions which are not according to the invention (Example 4) and which represent the prior art are the following: Nuva HPU (Clariant Corporation). Scotchgard.RTM. FC 396 (3M Comp.) according to DE-A 2 149 292 Baygard.RTM. SF-A. (Bayer AG) according to DE-A 3 307 420 and Zonyl (E. I. Dupont)
- The compositions according to the invention (Examples 1, 2 & 3) are non-aqueous solutions contents of which comprise a mixture of NPB (component A) and one or more poly (meth) acrylates (component B).
- A solution of 98% NPB and 2% Perfluoroalkyl polyacrylate were mixed and applied to the foam generator which imparts the solution to a high speed mixer that generates the solution into foam. The foam was then dispensed to the substrates listed in below via an applicator at 30%-wet pickup. The substrates were then dried at 170 deg C. for 1-minute dwell time with the following results:
Initial After 10 Home Laundries Example 1 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 5 85 100 2160 ppm 2 60 70 1600 ppm Polyester 6 90 100 1170 ppm 5 90 90 980 ppm Pes/Rayon 6 80 100 5 60 70 - A solution of 99.6% NPB and 0.4% Perfluoroalkyl polyacrylate were mixed and applied to the substrates listed below via a pad applicator at 3.5 bars pressure. The solution was applied at noted wet pickup. Again, the substrates were dried at 170 deg C. with a 1-minute dwell.
Initial After 10 Home Laundries Example 2 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 6 100 100 2480 ppm 3 90 80 2200 ppm Polyester 8 90 100 1270 ppm 6 90 90 1100 ppm Pes/Rayon 8 80 100 6 80 80 - A solution of 99.6% NPB and 2% Perfluoroalkyl polyacrylate were mixed and applied to the substrates listed below via a Spray at 1.5 bars pressure. The solution was applied at noted wet pickup. Again, the substrates were dried at 170 deg C. with a 1-minute dwell.
Initial After 10 Home Laundries Example 3 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 6 85 100 2260 ppm 2 60 70 1690 ppm Polyester 6 90 100 1170 ppm 5 90 90 1080 ppm Pes/Rayon 6 80 100 5 60 70 - An aqueous Perfluoroalkyl polyacrylate dispersion using Nuva HPU at 2% concentration was prepared and applied via a padding applicator at 3.5 bars pressure. The solution was applied at noted wet pickup. Again, the substrates were dried at 170 deg C. with a 1-minute dwell.
Initial After 10 H me Laundries Example 4 Oil IPA Spray Fluoride Oil IPA Spray Fluoride Cotton 7 100 100 2460 7 90 80 2210 ppm ppm Polyester 6 60 100 1270 4-5 45-50 90 1100 ppm ppm Pes/Rayon 5 60 100 2 35-40 70 - In all examples, the substrates used were (1) White Polyester 8 oz/sq yd (PES), (2) 100% Cotton interlock and (3) 60/40 PES and Rayon Blend.
Claims (15)
1. Methods and chemical formulations utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other chemicals to substrates, whereby the NPB is evaporated away leaving the remaining chemicals on the substrate.
2. Formula as set forth in claim 1 , Fluorine-containing compositions for oil-, water- and soil-repellant treatment of substrates, comprising two components A (NPB) and B (fluorine-containing copolymer) which comprises, based on the total weight of A, the following weight contents of comonomer (B):
0.002 to 50% by weight of (meth) acrylates containing perfluoroalkyl groups, of the formula
C.sub.n F.sub.2n+1--X--O--CO--CR.sup.1.dbd.CH.sub.2 (I).
3. Formula as set forth in claim 2 , whereby treatment of substrates, comprising two components A (NPB) and B (other fluoroine-containing compounds) which comprises, based on the total weight of A, the following weight contents of comonomer (B):
0.002 to 40% by weight of component A
4. Formula as set forth in claim 3 , whereby treatment of substrates, comprising two components A (NPB) and B (Ultraviolet light inhibitor compound) which comprises, based on the total weight of A, the following weight contents of comonomer (B):
0.002 to 20% by weight of component A
5. Formula as set forth in claim 4 , whereby treatment of substrates, comprising two components A (NPB) and B (Antistat compounds) which comprises, based on the total weight of A, the following weight contents of comonomer (B):
0.002 to 10% by weight of component A
6. Formula as set forth in claim 5 , whereby treatment of substrates, comprising two components A (NPB) and B (Foaming compounds) which comprises, based on the total weight of A, the following weight contents of comonomer (B):
0.002 to 18% by weight of component A
7. Formula as set forth in claim 6 , whereby treatment of substrates, comprising two components A (NPB) and B (Antibacterial compound) which comprises, based on the total weight of A, the following weight contents of comonomer (B):
0.002 to 15% by weight of component A
8. Formula as set forth in claim 7 , whereby treatment of substrates, comprising two components A (NPB) and B (softening and hand building compound) which comprises, based on the total weight of A, the following weight contents of comonomer (B)
0.002 to 20% by weight of component A
9. Formula as set forth in claim 8 , whereby treatment of substrates, comprising two components A (NPB) and B (resin compounds) which comprises, based on the total weight of A, the following weight contents of comonomer (B):
0.002 to 80% by weight of component A
10. Formula as set forth in claim 9 , whereby treatment of substrates, comprising two components A (NPB) and B (Urethane) which comprises, based on the total weight of A, the following weight contents of comonomer (B)
0.002 to 12% by weight of component A
11. Formula as set forth in claim 10 , whereby treatment of substrates, comprising the single component A(NPB) being used as scouring agent.
12. A method for applying formulas set forth in claims 2 through 11 with a substrate, comprising the acts of padding; applying the chemical mixture with the substrate forming a wet substrate; and removing the non-aqueous solvent from the wet substrate, leaving a substrate with remaining chemical solution.
13. Method as set forth in claim 12 , where by formula set forth in claims 2 through 11 are foamed onto substrtate.
14. Method as set forth in claim 13 , where by formula set forth in claims 2 through 11 are sprayed onto substrtate.
15. Method as set forth in claim 14 , where by formula set forth in claims 2 through 11 are coated onto substrtate.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/611,746 US20040006827A1 (en) | 2002-07-03 | 2003-06-30 | Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates |
| US11/254,201 US20060035798A1 (en) | 2003-06-30 | 2005-10-20 | Non-aqueous water and oil repellent compositions for a durable hydrophobic textile |
| US11/355,270 US20060135386A1 (en) | 2003-06-30 | 2006-02-15 | Chemical composition for a fire retardant textile |
| US11/443,687 US20060217279A1 (en) | 2003-06-30 | 2006-06-01 | Surface treatment compositions for foaming process |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US39421202P | 2002-07-03 | 2002-07-03 | |
| US10/611,746 US20040006827A1 (en) | 2002-07-03 | 2003-06-30 | Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates |
Related Child Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/254,201 Continuation-In-Part US20060035798A1 (en) | 2003-06-30 | 2005-10-20 | Non-aqueous water and oil repellent compositions for a durable hydrophobic textile |
| US11/355,270 Division US20060135386A1 (en) | 2003-06-30 | 2006-02-15 | Chemical composition for a fire retardant textile |
| US11/443,687 Continuation-In-Part US20060217279A1 (en) | 2003-06-30 | 2006-06-01 | Surface treatment compositions for foaming process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20040006827A1 true US20040006827A1 (en) | 2004-01-15 |
Family
ID=30115690
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/611,746 Abandoned US20040006827A1 (en) | 2002-07-03 | 2003-06-30 | Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates |
| US10/613,735 Abandoned US20040134421A1 (en) | 2002-07-03 | 2003-07-03 | Apparatus and method for applying chemicals to substrates via the use of nonaqueous solvents |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/613,735 Abandoned US20040134421A1 (en) | 2002-07-03 | 2003-07-03 | Apparatus and method for applying chemicals to substrates via the use of nonaqueous solvents |
Country Status (3)
| Country | Link |
|---|---|
| US (2) | US20040006827A1 (en) |
| AU (1) | AU2003249700A1 (en) |
| WO (1) | WO2004004924A2 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040134421A1 (en) * | 2002-07-03 | 2004-07-15 | Larry Rising | Apparatus and method for applying chemicals to substrates via the use of nonaqueous solvents |
| US20060105110A1 (en) * | 2004-11-18 | 2006-05-18 | Precision Fabrics Group, Inc. | Methods of finishing medical barrier fabrics |
| US7842625B1 (en) | 2006-10-26 | 2010-11-30 | Nano-Tex, Inc. | Methods for treating fabric to facilitate moisture transfer from one side to the other |
| US20120218285A1 (en) * | 2011-02-25 | 2012-08-30 | University Of Rochester | Methods and systems for treatment of vestibular disorders |
| US12343064B2 (en) | 2009-12-18 | 2025-07-01 | Atricure, Inc. | Adjustable clamp systems and methods |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5139879A (en) * | 1991-09-20 | 1992-08-18 | Allied-Signal Inc. | Fluoropolymer blend anti-reflection coatings and coated articles |
| US5827812A (en) * | 1995-05-16 | 1998-10-27 | Minnesota Mining And Manufacturing Company | Azeotrope-like compositions and their use |
| US6342471B1 (en) * | 2000-01-25 | 2002-01-29 | Toney M. Jackson | Electrical contact cleaner |
| US6699829B2 (en) * | 2002-06-07 | 2004-03-02 | Kyzen Corporation | Cleaning compositions containing dichloroethylene and six carbon alkoxy substituted perfluoro compounds |
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| US2717877A (en) * | 1952-09-10 | 1955-09-13 | American Cyanamid Co | Antistatic compositions |
| GB1082182A (en) * | 1965-01-15 | 1967-09-06 | Du Pont | Process for applying solvent-borne material to a travelling web |
| BE688969A (en) * | 1965-10-28 | 1967-04-27 | ||
| USRE27995E (en) * | 1968-10-31 | 1974-04-30 | Process for removal of moisture and/ok solvents from textile material | |
| US3593543A (en) * | 1969-05-26 | 1971-07-20 | Dow Chemical Co | Apparatus for treating fabrics from an organic solvent |
| US3617211A (en) * | 1969-07-08 | 1971-11-02 | Allied Chem | Phenyl glycol and short-chain halogenated hydrocarbon dye composition |
| IT1040457B (en) * | 1975-08-04 | 1979-12-20 | Rimar Spa | EQUIPMENT AND PROCEDURE FOR THE CONTINUOUS DYEING OF TEXTILE MANUFAT TI IN A SOLVENT BATH |
| US4136636A (en) * | 1977-09-26 | 1979-01-30 | B & K Machinery International Ltd. | Solvent vapor collector |
| US4421794A (en) * | 1980-05-30 | 1983-12-20 | James River Corporation | Solvent removal via continuously superheated heat transfer medium |
| US20040006827A1 (en) * | 2002-07-03 | 2004-01-15 | Rising Larry Ervin | Chemical formulations and methods utilizing NPB(n-propyl bromide) as non-aqueous carrier mediums to apply fluorocarbons and other organic chemicals to substrates |
-
2003
- 2003-06-30 US US10/611,746 patent/US20040006827A1/en not_active Abandoned
- 2003-07-03 AU AU2003249700A patent/AU2003249700A1/en not_active Abandoned
- 2003-07-03 US US10/613,735 patent/US20040134421A1/en not_active Abandoned
- 2003-07-03 WO PCT/US2003/021049 patent/WO2004004924A2/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5139879A (en) * | 1991-09-20 | 1992-08-18 | Allied-Signal Inc. | Fluoropolymer blend anti-reflection coatings and coated articles |
| US5827812A (en) * | 1995-05-16 | 1998-10-27 | Minnesota Mining And Manufacturing Company | Azeotrope-like compositions and their use |
| US6342471B1 (en) * | 2000-01-25 | 2002-01-29 | Toney M. Jackson | Electrical contact cleaner |
| US6699829B2 (en) * | 2002-06-07 | 2004-03-02 | Kyzen Corporation | Cleaning compositions containing dichloroethylene and six carbon alkoxy substituted perfluoro compounds |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040134421A1 (en) * | 2002-07-03 | 2004-07-15 | Larry Rising | Apparatus and method for applying chemicals to substrates via the use of nonaqueous solvents |
| US20060105110A1 (en) * | 2004-11-18 | 2006-05-18 | Precision Fabrics Group, Inc. | Methods of finishing medical barrier fabrics |
| US7208202B2 (en) | 2004-11-18 | 2007-04-24 | Precision Fabrics Group, Inc. | Methods of finishing medical barrier fabrics |
| US7842625B1 (en) | 2006-10-26 | 2010-11-30 | Nano-Tex, Inc. | Methods for treating fabric to facilitate moisture transfer from one side to the other |
| US12343064B2 (en) | 2009-12-18 | 2025-07-01 | Atricure, Inc. | Adjustable clamp systems and methods |
| US20120218285A1 (en) * | 2011-02-25 | 2012-08-30 | University Of Rochester | Methods and systems for treatment of vestibular disorders |
| US9167998B2 (en) * | 2011-02-25 | 2015-10-27 | University Of Rochester | Methods and systems for treatment of vestibular disorders |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004004924A2 (en) | 2004-01-15 |
| WO2004004924A3 (en) | 2004-04-01 |
| AU2003249700A1 (en) | 2004-01-23 |
| AU2003249700A8 (en) | 2004-01-23 |
| US20040134421A1 (en) | 2004-07-15 |
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Legal Events
| Date | Code | Title | Description |
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| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |