WO2016056931A1 - Method for impregnation of synthetic and natural fabrics - Google Patents
Method for impregnation of synthetic and natural fabrics Download PDFInfo
- Publication number
- WO2016056931A1 WO2016056931A1 PCT/PL2015/050052 PL2015050052W WO2016056931A1 WO 2016056931 A1 WO2016056931 A1 WO 2016056931A1 PL 2015050052 W PL2015050052 W PL 2015050052W WO 2016056931 A1 WO2016056931 A1 WO 2016056931A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- impregnation
- fabric
- water
- bath
- agents
- Prior art date
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 63
- 238000005470 impregnation Methods 0.000 title claims abstract description 44
- 238000000034 method Methods 0.000 title claims abstract description 35
- 239000000049 pigment Substances 0.000 claims abstract description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 229910052596 spinel Inorganic materials 0.000 claims abstract description 13
- 239000002518 antifoaming agent Substances 0.000 claims abstract description 12
- 239000002270 dispersing agent Substances 0.000 claims abstract description 12
- 229910052593 corundum Inorganic materials 0.000 claims abstract description 11
- 239000011230 binding agent Substances 0.000 claims abstract description 10
- 229910052595 hematite Inorganic materials 0.000 claims abstract description 10
- 239000011019 hematite Substances 0.000 claims abstract description 10
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000003899 bactericide agent Substances 0.000 claims abstract description 9
- 239000011029 spinel Substances 0.000 claims abstract description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000010431 corundum Substances 0.000 claims abstract description 6
- 229910052809 inorganic oxide Inorganic materials 0.000 claims abstract description 6
- 229910026161 MgAl2O4 Inorganic materials 0.000 claims abstract description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910001845 yogo sapphire Inorganic materials 0.000 claims abstract description 5
- 239000004815 dispersion polymer Substances 0.000 claims abstract description 3
- 230000001502 supplementing effect Effects 0.000 claims abstract description 3
- 229920000058 polyacrylate Polymers 0.000 claims description 14
- 239000000839 emulsion Substances 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 239000006185 dispersion Substances 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 6
- 229920001400 block copolymer Polymers 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 230000001747 exhibiting effect Effects 0.000 claims description 5
- 230000009477 glass transition Effects 0.000 claims description 5
- 239000012764 mineral filler Substances 0.000 claims description 5
- 239000004814 polyurethane Substances 0.000 claims description 5
- 229920002635 polyurethane Polymers 0.000 claims description 5
- 239000012752 auxiliary agent Substances 0.000 claims description 4
- VUWCWMOCWKCZTA-UHFFFAOYSA-N 1,2-thiazol-4-one Chemical class O=C1CSN=C1 VUWCWMOCWKCZTA-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- YABHQQLSFUHFHD-UHFFFAOYSA-N 2,3-dihydro-1,2-thiazole 1-oxide Chemical compound O=S1NCC=C1 YABHQQLSFUHFHD-UHFFFAOYSA-N 0.000 claims 1
- 230000005855 radiation Effects 0.000 description 15
- 238000010438 heat treatment Methods 0.000 description 11
- 238000000576 coating method Methods 0.000 description 8
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- 229910052804 chromium Inorganic materials 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 230000003595 spectral effect Effects 0.000 description 4
- 239000008199 coating composition Substances 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- 235000010215 titanium dioxide Nutrition 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 2
- 229920006243 acrylic copolymer Polymers 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000391 magnesium silicate Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000007655 standard test method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 238000001665 trituration Methods 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
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- YJVBLROMQZEFPA-UHFFFAOYSA-L acid red 26 Chemical compound [Na+].[Na+].CC1=CC(C)=CC=C1N=NC1=C(O)C(S([O-])(=O)=O)=CC2=CC(S([O-])(=O)=O)=CC=C12 YJVBLROMQZEFPA-UHFFFAOYSA-L 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007590 electrostatic spraying Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000012243 magnesium silicates Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000009418 renovation Methods 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/46—Oxides or hydroxides of elements of Groups 4 or 14 of the Periodic Table; Titanates; Zirconates; Stannates; Plumbates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/44—Oxides or hydroxides of elements of Groups 2 or 12 of the Periodic Table; Zincates; Cadmates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/45—Oxides or hydroxides of elements of Groups 3 or 13 of the Periodic Table; Aluminates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/49—Oxides or hydroxides of elements of Groups 8, 9,10 or 18 of the Periodic Table; Ferrates; Cobaltates; Nickelates; Ruthenates; Osmates; Rhodates; Iridates; Palladates; Platinates
-
- 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
-
- 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
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
-
- 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
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/647—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
-
- 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
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
-
- 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
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
- D06M23/08—Processes in which the treating agent is applied in powder or granular form
-
- 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
- D06M2200/25—Resistance to light or sun, i.e. protection of the textile itself as well as UV shielding materials or treatment compositions therefor; Anti-yellowing treatments
Definitions
- the invention relates to a method for impregnation of synthetic and natural fabrics, conferring especially properties of reflection of solar rays on the fabrics.
- the method is used particularly for coated fabrics used for production of window blinds, awnings, tourist equipment, such as tents, tarpaulins, sportswear etc.
- Grzelak "Ecological solar reflecting coatings for renovation of roof” , Izolacje, nr 4/2014, 38-41), relating to coatings with properties of reflection of solar radiation, protecting from excessive heating of surfaces and intended for wide range of applications - from application in building industry (so-called “cool roof for roofing or sidings), in road engineering (for road markings), in automotive industry (dashboards, car seats, car bodies etc.).
- the patent application EP2588543 Al discloses constitution of a binary coating composition conferring a reduced sensitivity to thermal deformation on products manufactured from thermoplastics.
- a binary coating composition conferring a reduced sensitivity to thermal deformation on products manufactured from thermoplastics.
- a well-adhesive coloured coating reflecting infrared radiation is formed after curing.
- the coating composition may be used for coating prefabricated products made of thermoplastics or their composites, such as: window frames, doors, siding panels, by commonly used methods: air spraying, airless spraying, electrostatic spraying, roller coating, glazing, and immersion.
- the patent application PL213433 discloses a water-dilutable coating composition containing pigments and fillers, and auxiliaries, consisting of 10% to 80% by wt. of a binder, constituted by water dispersions of an acrylic copolymer with a glass transition temperature (T g ) in the range of -25 °C to -15°C and preferably with a minimum film forming temperature (MFFT) of approx. 0°C, 20% to 60% by wt.
- T g glass transition temperature
- MFFT minimum film forming temperature
- a pigment mixture preferably titanium white and phthalocyanine blue or iron oxide black, and mineral fillers, preferably magnesium silicate and calcium carbonate or magnesium carbonate, including those with spherical and/or lamellar grain shape, 0.05% to 5% by wt. of a wetting and dispersing agent, preferably polyacrylic acid sodium salt, 0.10% to 5% by wt. of an antifoaming agent, preferably water emulsions of a polyethersiloxane, 0.1% to 10% by wt.
- a wetting and dispersing agent preferably polyacrylic acid sodium salt
- an antifoaming agent preferably water emulsions of a polyethersiloxane, 0.1% to 10% by wt.
- a rheological agent containing acrylic polymers preferably a 30% emulsion of a hydrophobically modified acrylic copolymer containing acrylic polymers and/or polyurethane polymers, preferably a 40% emulsion of a hydrophobically modified polyurethane, 0.05% to 2% by wt. of a bactericidal agent, preferably a mixture of isothiazolinones, and 0.0% to 2% of aqua ammonia.
- the share of a filler or fillers with spherical and/or lamellar grain shape in the total amount of mineral fillers is 1% to 90% by wt.-
- the conventional pigments applied, having a low value of the total solar reflectance (TSR) coefficient absorb a major part of solar radiation, causing - while exposed to sunlight - excessive heating of surfaces, particularly dark-coloured surfaces.
- the essence of the invention is constituted by a method for impregnation of synthetic and natural fabrics consisting in impregnation of a fabric in a bath containing a binder, at least one dispersing agent and at least one antifoaming agent characterised in the:
- the fabric is subject to impregnation in the bath composed of: 20 to 80% by wt. of a water-dilutable binder being a water polymer dispersion; 2 to 20% by wt. of dispersed inorganic oxide pigments with a crystallographic structure of rutile (Ti0 2 ), or spinel (MgAl 2 0 4 ), or hematite/corundum (Fe 2 0 3 /Al 2 0 3 ) with the total solar reflectance (TSR) value not lower than 20% and not higher than 99%; auxiliaries, including: 0.1 to 2% by wt. of dispersing agents, 0.05 to 2% of antifoaming agents, and 0.05 to 1,5% by wt. of bactericidal agents; and water in an amount supplementing the composition to 100% by wt.; and then, the so-impregnated fabric is dried at a temperature above 80°C.
- the binder is a water dispersion of an acrylic polymer, or a polyurethane polymer, or a polyurethane-acrylic polymer with a glass transition temperature (T g ) in the range of -5°C to +25 °C.
- T g glass transition temperature
- the polymer glass transition temperature (T g ) is in the range of 0°C to +5°C.
- the dispersed inorganic oxide pigments with a crystallographic structure of rutile (T1O 2 ) or spinel (MgAl 2 0 4 ) or hematite/corundum (Fe 2 0 3 /Al 2 0 3 ) have values of the total solar reflectance (TSR) coefficient not lower than 26% and not higher than 99%.
- the dispersing agent constitutes a 40% solution of a block copolymer with a high molecular mass and containing groups exhibiting affinity to the pigments' surface.
- the antifoaming agents are constituted by a water emulsion of a polyethersiloxane acid.
- the bactericidal agents constitute a mixture of isothiazolinones, most preferably a water solution of 5-chloro-2-methyl-4-isothiazolinone and 2-methyl-4- isothiazolinone.
- the impregnation bath additionally contains not more than 10% by wt. of classic coloured pigments.
- the impregnation bath additionally contains, as an auxiliary agent, not more than 2% by wt. of pH stabilisers.
- the impregnation bath additionally contains, as an auxiliary agent, not more than 5% by wt. of agents regulating the rheological properties of the bath.
- the agents regulating the rheological properties of the bath are constituted by a hydrophobically modified acrylic polymer.
- the impregnation bath additionally contains not more than 20% of mineral fillers.
- the fabric is dried at a temperature not higher than 150°C.
- the conventional colouring pigments include inorganic pigments, such as titanium white, iron oxide-based pigments such as iron oxide red, iron oxide black, ferrite yellow, and organic pigments, including carbon black.
- the mineral fillers which may be optionally used in the fabric impregnation method according to the invention, include calcium carbonates, magnesium silicates, aluminosilicates, silicas, and kaolins.
- the method for impregnation of synthetic and natural fabrics conferring properties of reflection of solar rays on them was achieved by using white and/or coloured pigments with an exceptional spectral characteristics for colouring of the impregnation bath.
- inorganic oxide pigments with a crystallographic structure of rutile, spinel or hematite/corundum were used for colouring of the impregnation bath.
- These pigments are characterised by a relatively high radiation reflectance in the range of near infrared.
- Application of pigments having a high value of the total solar reflectance (TSR) coefficient leads basically to a reduction of heating of their surface while exposed to solar radiation.
- TSR total solar reflectance
- the high TSR values of these pigments result from their ability to reflect the major part of solar radiation incident onto a surface coloured with them.
- the non-reflected radiation is absorbed by the surface or the substrate, and emitted in the form of long-wavelength thermal energy.
- the impregnation bath with the mentioned composition exhibits a very good stability and it may be stored for a period of up to six months.
- the method according to the invention may be carried out using machinery employed for the fabric impregnation. During drying of the fabrics, water evaporates and the polymer molecules coalesce forming a uniform coating, fixed to the fibre of the fabric. The process of drying of the fabrics impregnated using the method according to the invention is carried out at temperatures from 80 to 150°C in tunnel dryers.
- the fabrics impregnated using the method according to the invention exhibit a good elasticity, and when the impregnant is applied in the amount of approx. 300 ⁇ 50 g/m 2 depending on the type of the fabric, they are characterised by a low absorptivity of solar radiation.
- C.I.Pigment Brown 33 containing Fe, Cr, Zn, Ti (spinel) and having the 5.20 parts by wt.
- Dispersing agent - a 40% water solution of a block copolymer with a high 0.49 parts by wt.
- Antifoaming agent - a 30% emulsion of siloxylated polyethers in water 0.10 parts by wt.
- Thickening agent - a hydrophobically modified acrylic polymer 0.60 parts by wt.
- Bactericidal agent - a water solution of 5-chloro-2-mefhyl-4- 0.05 parts by wt.
- the pigments are pre-dispersed under a high-speed stirrer, and then dispersed in a bead mill, until a trituration degree of the pigments below 15 pm according to PN-EN 21524/AK: 1994 is obtained.
- an impregnation bath with the same colour was prepared using conventional pigments: red iron oxide and iron oxide black.
- the so-prepared baths are used to impregnate a viscose fabric with a grammage of 120 g/m 2 on an impregnation machine and the fabric is dried in a tunnel at a temperature from 80°C in the first chamber, do 120°C in the last chamber.
- the applied quantity of the impregnant is adjusted by regulating the size of the gap of the top rollers, and the efficiency of drying - by regulating the fabric travel speed.
- the fabric impregnated in the bath according to Example 1 is characterised by a high appret durability and a low absorptivity of solar radiation.
- the fabrics may be used for production of window blinds preventing heating of rooms.
- TSR value was determined according to ASTM E903-12 "Standard Test Method for Solar Absorptance, Reflectance and Transmittance of Materials Using Integrating Spheres" using a double-beam spectrophotometer UV/VIS/NIR V-670 with an integrating sphere. Heating of surfaces of both fabrics, measured as the temperature increase using a pyrometer, was examined in a heating chamber designed and constructed according to ASTM D4803-10 "Standard Test Method for Predicting Heat Buildup in PVC Building Products" and in the field, on a hot day with an air temperature of 30°C. The results are shown below in Table 2. Table 2.
- the obtained results indicate a significant influence of the fabric impregnation method on the heating of the fabric surface and the ability to design the radiation properties of the material.
- a significantly higher TSR value (28%) for the fabric impregnated according to Example 1 than that for the fabric impregnated in the conventional way (7%) contributes into a significantly less intense heating of the fabric impregnated according to Example 1, being confirmed by lower temperatures of the fabric surface while compared to the one impregnated in the conventional way, both in the test acc. to ASTM D4803-10, and in the field.
- Dispersing agent - a 40% water solution of a block copolymer with a 0.50 parts by wt.
- Antifoaming agent - a 30% emulsion of siloxylated polyethers in water 0.10 parts by wt.
- Thickening agent - a hydrophobically modified acrylic polymer 0.60 parts by wt.
- Bactericidal agent - a water solution of 5-chloro-2-mefhyl-4- 0.05 parts by wt.
- Example 2 the so-prepared mixtures are used analogically as in Example 1, with the exception that the baths are used to impregnate a viscose fabric with a grammage of 120 g/m 2 on an impregnation machine and the fabric is dried in a tunnel at a temperature from 80°C in the first chamber, do 150°C in the last chamber. Measurements of spectral properties of the fabric impregnated according to the Example 2 and the one impregnated according to the conventional method were carried out. The results are shown below in Table 4.
- Dispersing agent - a 40% water solution of a block copolymer with a high 0.50 parts by wt.
- Antifoaming agent - a 30% emulsion of siloxylated polyethers in water 0.10 parts by wt.
- Thickening agent - a hydrophobically modified acrylic polymer 0.55 parts by wt.
- Bactericidal agent - a water solution of 5-chloro-2-mefhyl-4- 0.05 parts by wt.
- the method for impregnation of fabrics according to the invention enables manufacturing of fabrics and products utilising them, with novel, exceptional properties, reflecting solar radiation, thanks to which the surfaces exposed to sunlight remain cool.
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Abstract
Method for impregnation of synthetic and natural fabrics consisting in the fabric impregnation in a bath containing a binder, at least one dispersing agent, and at least one antifoaming agent, characterised in that the fabric is subject to impregnation in the bath composed of 20 to 80% by wt. of a water-dilutable binder being a water polymer dispersion; 2 to 20% by wt. of dispersed inorganic oxide pigments with a crystallographic structure of rutile (TiO2) or spinel (MgAl2O4) or hematite/corundum (Fe2O3/Al2O3) with the total solar reflectance (TSR) value not lower than 20% and not higher than 99%; auxiliaries, including: 0.1 to 2% by wt. of dispersing agents, 0.05 to 2% of antifoaming agents, and 0.05 to 1,5% by wt. of bactericidal agents, and water in an amount supplementing the composition to 100% by wt.; and then, the so-impregnated fabric is dried at a temperature above 80°C.
Description
Method for impregnation of synthetic and natural fabrics
The invention relates to a method for impregnation of synthetic and natural fabrics, conferring especially properties of reflection of solar rays on the fabrics. The method is used particularly for coated fabrics used for production of window blinds, awnings, tourist equipment, such as tents, tarpaulins, sportswear etc.
Various methods for modification of surface of woven fabrics and/or synthetic and natural fibres are known, consisting in coating them with a layer of an impregnant in order to obtain the required properties. Most often, the impregnation of synthetic and natural fabrics commonly used in the textile industry gives the surfaces of the fabrics hydrophobic properties increasing waterproofness, reducing the tendency to become dirty, facilitating cleaning, or provides the fabrics with bacteri- and fungicidal (patent application PL215349 Bl), antistatic and/or flame retardant (patent application PL134689) properties. The enumerated methods for the fabric impregnation with formation of coatings having specific usable features do not protect these materials from being heated in the result of absorption of solar radiation, particularly in the infrared range (700 - 2500 nm), subsequently emitted in the form of thermal energy.
For several years now, literature reports are being published (H.Akbari, H.D.Mathews "Global cooling updates: Reflective roofs and pavements" Energy and Buildings, Vol. 55, December 2012, 2-6; "Cool-Color Roofing Material" PIER Final Project Report, 2006; R. Doyle, www.pcimag.com Understanding Cool Coatings for Automotive, 2009; E. Langer, H. Kuczynska, M. Grzelak "Ecological solar reflecting coatings for renovation of roof" , Izolacje, nr 4/2014, 38-41), relating to coatings with properties of reflection of solar radiation, protecting from excessive heating of surfaces and intended for wide range of applications - from application in building industry (so-called "cool roof for roofing or sidings), in road engineering (for road markings), in automotive industry (dashboards, car seats, car bodies etc.).
The patent application EP2588543 Al discloses constitution of a binary coating composition conferring a reduced sensitivity to thermal deformation on products manufactured from thermoplastics. In the results of application of this composition containing a water- dilutable binder with active hydroxyl groups, a water-dispersible polyisocyanate, and a coloured pigment not absorbing infrared radiation, a well-adhesive coloured coating reflecting infrared
radiation is formed after curing. The coating composition may be used for coating prefabricated products made of thermoplastics or their composites, such as: window frames, doors, siding panels, by commonly used methods: air spraying, airless spraying, electrostatic spraying, roller coating, glazing, and immersion.
The patent application PL213433 discloses a water-dilutable coating composition containing pigments and fillers, and auxiliaries, consisting of 10% to 80% by wt. of a binder, constituted by water dispersions of an acrylic copolymer with a glass transition temperature (Tg) in the range of -25 °C to -15°C and preferably with a minimum film forming temperature (MFFT) of approx. 0°C, 20% to 60% by wt. of a pigment mixture, preferably titanium white and phthalocyanine blue or iron oxide black, and mineral fillers, preferably magnesium silicate and calcium carbonate or magnesium carbonate, including those with spherical and/or lamellar grain shape, 0.05% to 5% by wt. of a wetting and dispersing agent, preferably polyacrylic acid sodium salt, 0.10% to 5% by wt. of an antifoaming agent, preferably water emulsions of a polyethersiloxane, 0.1% to 10% by wt. of a rheological agent containing acrylic polymers, preferably a 30% emulsion of a hydrophobically modified acrylic copolymer containing acrylic polymers and/or polyurethane polymers, preferably a 40% emulsion of a hydrophobically modified polyurethane, 0.05% to 2% by wt. of a bactericidal agent, preferably a mixture of isothiazolinones, and 0.0% to 2% of aqua ammonia. The share of a filler or fillers with spherical and/or lamellar grain shape in the total amount of mineral fillers is 1% to 90% by wt.-The conventional pigments applied, having a low value of the total solar reflectance (TSR) coefficient absorb a major part of solar radiation, causing - while exposed to sunlight - excessive heating of surfaces, particularly dark-coloured surfaces.
Solutions known from the state of art do not disclose any method for impregnation of synthetic and natural fabrics providing properties of reflection of solar rays for these products.
The essence of the invention is constituted by a method for impregnation of synthetic and natural fabrics consisting in impregnation of a fabric in a bath containing a binder, at least one dispersing agent and at least one antifoaming agent characterised in the:
the fabric is subject to impregnation in the bath composed of: 20 to 80% by wt. of a water-dilutable binder being a water polymer dispersion; 2 to 20% by wt. of dispersed inorganic oxide pigments with a crystallographic structure of rutile (Ti02), or spinel (MgAl204), or hematite/corundum (Fe203/Al203) with the total solar reflectance (TSR) value not lower than 20% and not higher than 99%; auxiliaries, including: 0.1 to 2% by wt. of dispersing agents, 0.05 to 2% of antifoaming agents, and 0.05 to 1,5% by wt. of bactericidal agents; and water in an amount supplementing the composition to 100% by wt.;
and then, the so-impregnated fabric is dried at a temperature above 80°C.
Preferably, the binder is a water dispersion of an acrylic polymer, or a polyurethane polymer, or a polyurethane-acrylic polymer with a glass transition temperature (Tg) in the range of -5°C to +25 °C. Especially preferably, the polymer glass transition temperature (Tg) is in the range of 0°C to +5°C.
Equally preferably, the dispersed inorganic oxide pigments with a crystallographic structure of rutile (T1O2) or spinel (MgAl204) or hematite/corundum (Fe203/Al203) have values of the total solar reflectance (TSR) coefficient not lower than 26% and not higher than 99%.
Preferably, the dispersing agent constitutes a 40% solution of a block copolymer with a high molecular mass and containing groups exhibiting affinity to the pigments' surface. Equally preferably, the antifoaming agents are constituted by a water emulsion of a polyethersiloxane acid. Also preferably, the bactericidal agents constitute a mixture of isothiazolinones, most preferably a water solution of 5-chloro-2-methyl-4-isothiazolinone and 2-methyl-4- isothiazolinone.
Preferably, the impregnation bath additionally contains not more than 10% by wt. of classic coloured pigments. Equally preferably, the impregnation bath additionally contains, as an auxiliary agent, not more than 2% by wt. of pH stabilisers.
Preferably, the impregnation bath additionally contains, as an auxiliary agent, not more than 5% by wt. of agents regulating the rheological properties of the bath. Especially preferably, the agents regulating the rheological properties of the bath are constituted by a hydrophobically modified acrylic polymer.
Preferably, the impregnation bath additionally contains not more than 20% of mineral fillers.
Also preferably, the fabric is dried at a temperature not higher than 150°C.
The conventional colouring pigments include inorganic pigments, such as titanium white, iron oxide-based pigments such as iron oxide red, iron oxide black, ferrite yellow, and organic pigments, including carbon black.
The mineral fillers, which may be optionally used in the fabric impregnation method according to the invention, include calcium carbonates, magnesium silicates, aluminosilicates, silicas, and kaolins.
The method for impregnation of synthetic and natural fabrics conferring properties of reflection of solar rays on them was achieved by using white and/or coloured pigments with an exceptional spectral characteristics for colouring of the impregnation bath.
In the fabric impregnation method, inorganic oxide pigments with a crystallographic structure of rutile, spinel or hematite/corundum were used for colouring of the impregnation bath. These pigments are characterised by a relatively high radiation reflectance in the range of near infrared. Application of pigments having a high value of the total solar reflectance (TSR) coefficient leads basically to a reduction of heating of their surface while exposed to solar radiation. The high TSR values of these pigments result from their ability to reflect the major part of solar radiation incident onto a surface coloured with them. The non-reflected radiation is absorbed by the surface or the substrate, and emitted in the form of long-wavelength thermal energy.
The impregnation bath with the mentioned composition exhibits a very good stability and it may be stored for a period of up to six months. The method according to the invention may be carried out using machinery employed for the fabric impregnation. During drying of the fabrics, water evaporates and the polymer molecules coalesce forming a uniform coating, fixed to the fibre of the fabric. The process of drying of the fabrics impregnated using the method according to the invention is carried out at temperatures from 80 to 150°C in tunnel dryers. The fabrics impregnated using the method according to the invention exhibit a good elasticity, and when the impregnant is applied in the amount of approx. 300±50 g/m2 depending on the type of the fabric, they are characterised by a low absorptivity of solar radiation.
Application of the method for impregnation of synthetic and natural fabrics conferring the properties of reflection of solar rays on them according to the invention allows for counteracting the effects of excessive solar radiation and simultaneously: a) in case of window blinds - it yields a reduction in the temperatures in rooms and a comfort improvement, power savings connected with a reduction or elimination of air-conditioning use, b) in case of tourist equipment and sportswear - it yields a reduction in their heating and therefore a comfort improvement for the user, c) it increases the durability of the products while exposed to solar radiation.
The subject of the invention is shown in more detail in the following embodiment examples.
Example 1
For the fabric impregnation, a bath with the following composition shown in Table 1 was prepared, having chocolate brown colour according to the RAL 8017 colour standard:
Table 1.
1. Water dispersion of an acrylic polymer with Tg = -3°C 30.40 parts by wt.
2. C.I.Pigment Brown 33 containing Fe, Cr, Zn, Ti (spinel) and having the 5.20 parts by wt.
TSR value of 38%
3. C.I.Pigment Green 17 containing Fe, Cr (hematite) and having the TSR 8.87 parts by wt.
value of 26%
4. C.I.Pigment Red 101 (iron oxide red Fe203) 0.33 parts by wt.
5. Dispersing agent - a 40% water solution of a block copolymer with a high 0.49 parts by wt.
molecular mass, containing groups exhibiting affinity to the pigments' surface
6. Antifoaming agent - a 30% emulsion of siloxylated polyethers in water 0.10 parts by wt.
7. Thickening agent - a hydrophobically modified acrylic polymer 0.60 parts by wt.
8. Bactericidal agent - a water solution of 5-chloro-2-mefhyl-4- 0.05 parts by wt.
isothiazolinone and 2-methyl-4-isothiazolinone
9. Water 53.96 parts by wt.
100.00 parts by wt.
The pigments are pre-dispersed under a high-speed stirrer, and then dispersed in a bead mill, until a trituration degree of the pigments below 15 pm according to PN-EN 21524/AK: 1994 is obtained. For comparison of properties of the prepared impregnation bath according to Example 1, an impregnation bath with the same colour was prepared using conventional pigments: red iron oxide and iron oxide black.
The so-prepared baths are used to impregnate a viscose fabric with a grammage of 120 g/m2 on an impregnation machine and the fabric is dried in a tunnel at a temperature from 80°C in the first chamber, do 120°C in the last chamber. The applied quantity of the impregnant is adjusted by regulating the size of the gap of the top rollers, and the efficiency of drying - by regulating the fabric travel speed. The fabric impregnated in the bath according to Example 1 is characterised by a high appret durability and a low absorptivity of solar radiation. The fabrics may be used for production of window blinds preventing heating of rooms.
This is confirmed by measurements of spectral properties of the fabric impregnated according to the Example 1 and the one impregnated according to the conventional method. The TSR value was determined according to ASTM E903-12 "Standard Test Method for Solar Absorptance, Reflectance and Transmittance of Materials Using Integrating Spheres" using a double-beam spectrophotometer UV/VIS/NIR V-670 with an integrating sphere. Heating of surfaces of both fabrics, measured as the temperature increase using a pyrometer, was examined in a heating chamber designed and constructed according to ASTM D4803-10 "Standard Test Method for Predicting Heat Buildup in PVC Building Products" and in the field, on a hot day with an air temperature of 30°C. The results are shown below in Table 2.
Table 2.
The obtained results indicate a significant influence of the fabric impregnation method on the heating of the fabric surface and the ability to design the radiation properties of the material. A significantly higher TSR value (28%) for the fabric impregnated according to Example 1 than that for the fabric impregnated in the conventional way (7%) contributes into a significantly less intense heating of the fabric impregnated according to Example 1, being confirmed by lower temperatures of the fabric surface while compared to the one impregnated in the conventional way, both in the test acc. to ASTM D4803-10, and in the field.
Example 2
For the fabric impregnation, a bath with the following composition shown in Table 3 was prepared, having window grey colour according to the RAL 7040 colour standard:
Table 3.
1. Water dispersion of an acrylic polymer with Tg = 0°C 32.00 parts by wt.
2. C.I.Pigment White 6 containing Ti02 (rutile) and having the TSR value 1.50 parts by wt.
of 86 %
3. C.I.Pigment Green 17 containing Fe, Cr (hematite) and having the TSR 4.12 parts by wt.
value of 28%
4. C.I.Pigment Blue 36 containing Co, Cr, Al (spinel) and having the TSR 0.23 parts by wt.
value of 31%
5. Dispersing agent - a 40% water solution of a block copolymer with a 0.50 parts by wt.
high molecular mass, containing groups exhibiting affinity to the
pigments' surface
6. Antifoaming agent - a 30% emulsion of siloxylated polyethers in water 0.10 parts by wt.
7. Thickening agent - a hydrophobically modified acrylic polymer 0.60 parts by wt.
8. Bactericidal agent - a water solution of 5-chloro-2-mefhyl-4- 0.05 parts by wt.
isothiazolinone and 2-methyl-4-isothiazolinone
9. Water 60.90 parts by wt.
100.00 parts by wt.
The pigments are pre-dispersed under a high-speed stirrer, and then dispersed in a bead mill, until a trituration degree of the pigments below 15 μιη according to PN-EN 21524/AK: 1994 is obtained. For comparison of the properties of the prepared impregnation bath according to Example 1, an impregnation bath with the same colour was prepared using conventional pigments: rutile-type titanium white and iron oxide black.
Then, the so-prepared mixtures are used analogically as in Example 1, with the exception that the baths are used to impregnate a viscose fabric with a grammage of 120 g/m2 on an impregnation machine and the fabric is dried in a tunnel at a temperature from 80°C in the first chamber, do 150°C in the last chamber. Measurements of spectral properties of the fabric impregnated according to the Example 2 and the one impregnated according to the conventional method were carried out. The results are shown below in Table 4.
Table 4.
The obtained results, similarly as in Example 1, indicate a significant influence of the fabric impregnation method on the heating of the fabric surface. A significantly higher TSR value (48%) for the fabric impregnated according to Example 2 than that for the fabric impregnated in the conventional way (15%) contributes into a significantly less intense heating of the fabric impregnated according to Example 1, being confirmed by lower temperatures of the fabric surface while compared to the one impregnated in the conventional way, both in the test acc. to ASTM D4803-10, and in the field.
Example 3
For the fabric impregnation, a bath with the following composition , having olive green colour according to the RAL 6003 colour standard.
Table 5.
1. Water dispersion of an acrylic polymer with Tg = -3°C 38.00 parts by wt.
2. C.I.Pigment Brown 29 containing Fe, Cr (hematite) and having the TSR 1.00 parts by wt.
value of 29%
3. C.I.Pigment Green 17 containing Fe, Cr (hematite) and having the TSR 4.32 parts by wt.
value of 40%
4. Talc 8.00 parts by wt.
5. Dispersing agent - a 40% water solution of a block copolymer with a high 0.50 parts by wt.
molecular mass, containing groups exhibiting affinity to the pigments' surface
6. Antifoaming agent - a 30% emulsion of siloxylated polyethers in water 0.10 parts by wt.
7. Thickening agent - a hydrophobically modified acrylic polymer 0.55 parts by wt.
8. Bactericidal agent - a water solution of 5-chloro-2-mefhyl-4- 0.05 parts by wt.
isothiazolinone and 2-methyl-4-isothiazolinone
9. Water 47.48 parts by wt.
100.00 parts by wt.
The method for the impregnant preparation and the fabric impregnation is the same as reported for Examples 1 and 2. Measurements of spectral properties of the fabric impregnated according to the Example 3 and the one impregnated according to the conventional method were carried out. The results are shown below in Table 6.
Table 6.
The method for impregnation of fabrics according to the invention enables manufacturing of fabrics and products utilising them, with novel, exceptional properties, reflecting solar radiation, thanks to which the surfaces exposed to sunlight remain cool.
Claims
1. Method for impregnation of synthetic and natural fabrics consisting in the fabric
impregnation in a bath containing a binder, at least one dispersing agent, and at least one antifoaming agent, wherein the fabric is subject to impregnation in the bath composed of: a. 20 to 80% by wt. of a water-dilutable binder being a water polymer dispersion, b. 2 to 20% by wt. of dispersed inorganic oxide pigments with a crystallographic structure of rutile (T1O2) or spinel (MgAl204) or hematite/corundum (Fe203/Al203) with the total solar reflectance (TSR) value not lower than 20% and not higher than
99%,
c. auxiliaries, including: 0.1 to 2% by wt. of dispersing agents, 0.05 to 2% of
antifoaming agents, and 0.05 to 1,5% by wt. of bactericidal agents; and d. water in an amount supplementing the composition to 100 % by wt.,
and then, the so-impregnated fabric is dried at a temperature above 80°C.
2. The method according to claim 1, wherein the binder is a water dispersion of an acrylic polymer, or a polyurethane polymer, or a polyurethane -acrylic polymer with a glass transition temperature (Tg) in the range of -5°C to +25°C.
3. The method according to claim 2, wherein the polymer glass transition temperature (Tg) is in the range of 0°C to +5°C.
4. The method according to claim 1, wherein the dispersed inorganic oxide pigments with a crystallographic structure of rutile (T1O2) or spinel (MgAl204) or hematite/corundum (Fe203/Al203) have values of the total solar reflectance (TSR) coefficient not lower than 26% and not higher than 99%.
5. The method according to claim 1, wherein dispersing agent are constituted by a 40%
solution of a block copolymer with a high molecular mass and containing groups exhibiting affinity to the pigments' surface.
6. The method according to claim 1, wherein the antifoaming agents are constituted by a water emulsion of a polyethersiloxane acid.
7. The method according to claim 1, wherein the bactericidal agents constitute a mixture of isothiazolinones, most preferably a water solution 5 -chloro-2 -methyl -4-isothiazolinone and 2-methy 1-4-isothiazolinone .
8. The method according to claim 1, wherein the impregnation bath additionally contains not more than 10% by wt. of classic coloured pigments.
9. The method according to claim 1, wherein the impregnation bath additionally contains, as an auxiliary agent, not more than 2% by wt. of pH stabilisers.
10. The method according to claim 1, wherein the impregnation bath additionally contains, as an auxiliary agent, not more than 5% by wt. of agents regulating the rheological properties of the bath.
11. The method according to claim 10, wherein the agents regulating the rheological properties of the bath are constituted by a hydrophobically modified acrylic polymer.
12. The method according to claim 1, wherein the impregnation bath additionally contains not more than 20% of mineral fillers.
13. The method according to claim 1, wherein the fabric is dried at a temperature not higher than 150°C.
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PL409710A PL409710A1 (en) | 2014-10-06 | 2014-10-06 | Method for impregnation of synthetic and natural textiles |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PL213433A1 (en) | 1979-02-13 | 1980-09-08 | Inst Chemii Nieorganicznej | |
PL134689B1 (en) | 1983-04-12 | 1985-09-30 | Glowny Instytut Gornictwa | Method of impregnation of synthetic and natural fabrics,imparting to them slow-burning and antistatic properties |
CN101435158A (en) * | 2008-12-29 | 2009-05-20 | 郑州优波科新材料有限公司 | Heat insulating coating for textile |
US20100047620A1 (en) * | 2007-02-05 | 2010-02-25 | Ppg Industries Ohio, Inc. | Solar reflective coatings and coating systems |
EP2588543A1 (en) | 2010-07-01 | 2013-05-08 | Valspar Sourcing, Inc. | Infrared-reflective two-part coating composition |
PL215349B1 (en) | 2009-04-02 | 2013-11-29 | Politechnika Gdanska | Method of the fabric impregnation with the particles of nanosilver |
-
2014
- 2014-10-06 PL PL409710A patent/PL409710A1/en unknown
-
2015
- 2015-10-05 WO PCT/PL2015/050052 patent/WO2016056931A1/en active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PL213433A1 (en) | 1979-02-13 | 1980-09-08 | Inst Chemii Nieorganicznej | |
PL134689B1 (en) | 1983-04-12 | 1985-09-30 | Glowny Instytut Gornictwa | Method of impregnation of synthetic and natural fabrics,imparting to them slow-burning and antistatic properties |
US20100047620A1 (en) * | 2007-02-05 | 2010-02-25 | Ppg Industries Ohio, Inc. | Solar reflective coatings and coating systems |
CN101435158A (en) * | 2008-12-29 | 2009-05-20 | 郑州优波科新材料有限公司 | Heat insulating coating for textile |
PL215349B1 (en) | 2009-04-02 | 2013-11-29 | Politechnika Gdanska | Method of the fabric impregnation with the particles of nanosilver |
EP2588543A1 (en) | 2010-07-01 | 2013-05-08 | Valspar Sourcing, Inc. | Infrared-reflective two-part coating composition |
Non-Patent Citations (4)
Title |
---|
E. LANGER; H. KUCZYNSKA; M. GRZELAK: "Ecological solar reflecting coatings for renovation of roof", IZOLACJE, 2014, pages 38 - 41 |
H.AKBARI; H.D.MATHEWS: "Global cooling updates: Reflective roofs and pavements", ENERGY AND BUILDINGS, vol. 55, December 2012 (2012-12-01), pages 2 - 6 |
PIER FINAL PROJECT REPORT, COOL-COLOR ROOFING MATERIAL, 2006 |
R. DOYLE, UNDERSTANDING COOL COATINGS FOR AUTOMOTIVE, 2009, Retrieved from the Internet <URL:www.pcimag.com> |
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