WO2021091366A1 - Polymeric/inorganic composite particle formulation and methods of producing rubber articles using said formulation - Google Patents
Polymeric/inorganic composite particle formulation and methods of producing rubber articles using said formulation Download PDFInfo
- Publication number
- WO2021091366A1 WO2021091366A1 PCT/MY2020/000008 MY2020000008W WO2021091366A1 WO 2021091366 A1 WO2021091366 A1 WO 2021091366A1 MY 2020000008 W MY2020000008 W MY 2020000008W WO 2021091366 A1 WO2021091366 A1 WO 2021091366A1
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- Prior art keywords
- formulation
- former
- rubber
- latex
- concentration
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 391
- 238000009472 formulation Methods 0.000 title claims abstract description 337
- 238000000034 method Methods 0.000 title claims abstract description 219
- 229920001971 elastomer Polymers 0.000 title claims abstract description 189
- 239000005060 rubber Substances 0.000 title claims abstract description 189
- 239000011246 composite particle Substances 0.000 title claims abstract description 134
- 239000004815 dispersion polymer Substances 0.000 claims abstract description 72
- 239000002270 dispersing agent Substances 0.000 claims abstract description 20
- 239000003002 pH adjusting agent Substances 0.000 claims abstract description 16
- 239000010954 inorganic particle Substances 0.000 claims abstract description 11
- 239000010410 layer Substances 0.000 claims description 162
- 229920000126 latex Polymers 0.000 claims description 152
- 239000004816 latex Substances 0.000 claims description 152
- 239000010408 film Substances 0.000 claims description 143
- 229920000459 Nitrile rubber Polymers 0.000 claims description 75
- 239000000080 wetting agent Substances 0.000 claims description 65
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 58
- 239000002131 composite material Substances 0.000 claims description 55
- 150000003839 salts Chemical class 0.000 claims description 55
- 229910010272 inorganic material Inorganic materials 0.000 claims description 53
- 239000011147 inorganic material Substances 0.000 claims description 52
- 230000005855 radiation Effects 0.000 claims description 50
- 230000001112 coagulating effect Effects 0.000 claims description 48
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 45
- 229920005549 butyl rubber Polymers 0.000 claims description 44
- 239000011358 absorbing material Substances 0.000 claims description 41
- 238000001035 drying Methods 0.000 claims description 40
- 229910001385 heavy metal Inorganic materials 0.000 claims description 40
- 229910052751 metal Inorganic materials 0.000 claims description 40
- 239000002184 metal Substances 0.000 claims description 40
- 239000006254 rheological additive Substances 0.000 claims description 31
- 239000000654 additive Substances 0.000 claims description 30
- 239000013049 sediment Substances 0.000 claims description 30
- 239000004814 polyurethane Substances 0.000 claims description 29
- 238000000465 moulding Methods 0.000 claims description 27
- 239000002245 particle Substances 0.000 claims description 27
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 25
- 239000002253 acid Substances 0.000 claims description 25
- 229920006173 natural rubber latex Polymers 0.000 claims description 24
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 claims description 22
- JLDSOYXADOWAKB-UHFFFAOYSA-N aluminium nitrate Chemical compound [Al+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O JLDSOYXADOWAKB-UHFFFAOYSA-N 0.000 claims description 20
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 20
- 239000006228 supernatant Substances 0.000 claims description 20
- 230000000996 additive effect Effects 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 19
- 229920001195 polyisoprene Polymers 0.000 claims description 19
- 239000004800 polyvinyl chloride Substances 0.000 claims description 17
- 239000006185 dispersion Substances 0.000 claims description 16
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 13
- 239000005864 Sulphur Substances 0.000 claims description 13
- 150000002736 metal compounds Chemical class 0.000 claims description 13
- 239000000843 powder Substances 0.000 claims description 13
- 229920003051 synthetic elastomer Polymers 0.000 claims description 13
- 239000000230 xanthan gum Substances 0.000 claims description 13
- 229920001285 xanthan gum Polymers 0.000 claims description 13
- 229940082509 xanthan gum Drugs 0.000 claims description 13
- 235000010493 xanthan gum Nutrition 0.000 claims description 13
- 239000004952 Polyamide Substances 0.000 claims description 12
- 239000012670 alkaline solution Substances 0.000 claims description 12
- 239000000956 alloy Substances 0.000 claims description 12
- 229910045601 alloy Inorganic materials 0.000 claims description 12
- 239000004927 clay Substances 0.000 claims description 12
- 239000008380 degradant Substances 0.000 claims description 12
- 239000000696 magnetic material Substances 0.000 claims description 12
- 229920000609 methyl cellulose Polymers 0.000 claims description 12
- 239000001923 methylcellulose Substances 0.000 claims description 12
- 235000010981 methylcellulose Nutrition 0.000 claims description 12
- 229920000058 polyacrylate Polymers 0.000 claims description 12
- 229920002647 polyamide Polymers 0.000 claims description 12
- 229920002635 polyurethane Polymers 0.000 claims description 12
- 229920003009 polyurethane dispersion Polymers 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 12
- 238000004073 vulcanization Methods 0.000 claims description 12
- 239000011787 zinc oxide Substances 0.000 claims description 12
- 239000002736 nonionic surfactant Substances 0.000 claims description 10
- 239000002356 single layer Substances 0.000 claims description 10
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 9
- 239000001110 calcium chloride Substances 0.000 claims description 9
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 9
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 8
- 238000002386 leaching Methods 0.000 claims description 7
- 239000010409 thin film Substances 0.000 claims description 3
- 239000003607 modifier Substances 0.000 claims 1
- 239000000701 coagulant Substances 0.000 description 17
- 229920000642 polymer Polymers 0.000 description 14
- 244000043261 Hevea brasiliensis Species 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 229920003052 natural elastomer Polymers 0.000 description 6
- 229920001194 natural rubber Polymers 0.000 description 6
- 238000004062 sedimentation Methods 0.000 description 6
- 238000013019 agitation Methods 0.000 description 5
- 238000007598 dipping method Methods 0.000 description 5
- 238000005054 agglomeration Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910000416 bismuth oxide Inorganic materials 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 description 4
- 102000004169 proteins and genes Human genes 0.000 description 4
- 108090000623 proteins and genes Proteins 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 3
- 230000002009 allergenic effect Effects 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- 230000032798 delamination Effects 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000007815 allergy Effects 0.000 description 2
- 229920005601 base polymer Polymers 0.000 description 2
- 230000021523 carboxylation Effects 0.000 description 2
- 238000006473 carboxylation reaction Methods 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229910003439 heavy metal oxide Inorganic materials 0.000 description 2
- 229910003471 inorganic composite material Inorganic materials 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical group 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- -1 day Polymers 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L13/00—Compositions of rubbers containing carboxyl groups
- C08L13/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/02—Direct processing of dispersions, e.g. latex, to articles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/06—Sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L11/00—Compositions of homopolymers or copolymers of chloroprene
- C08L11/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L19/00—Compositions of rubbers not provided for in groups C08L7/00 - C08L17/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
- C08L7/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/02—Copolymers with acrylonitrile
- C08L9/04—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/06—Copolymers with styrene
- C08L9/08—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/10—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2307/00—Characterised by the use of natural rubber
- C08J2307/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2309/00—Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
- C08J2309/02—Copolymers with acrylonitrile
- C08J2309/04—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2309/00—Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
- C08J2309/06—Copolymers with styrene
- C08J2309/08—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2309/00—Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
- C08J2309/10—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2311/00—Characterised by the use of homopolymers or copolymers of chloroprene
- C08J2311/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2313/00—Characterised by the use of rubbers containing carboxyl groups
- C08J2313/02—Latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2319/00—Characterised by the use of rubbers not provided for in groups C08J2307/00 - C08J2317/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2237—Oxides; Hydroxides of metals of titanium
- C08K2003/2241—Titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2296—Oxides; Hydroxides of metals of zinc
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/01—Magnetic additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/08—Metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
Definitions
- the present invention relates to a formulation of polymeric/inorganic composite particles and methods of producing rubber articles using said formulation.
- High atomic weight elements and their compounds have been used in rubber articles due to their intrinsic property of absorbing ionising radiation which is useful for detection by ionising radiation or ionising radiation shielding.
- the use of blends of particulate inorganic compounds of high atomic weight elements and aqueous polymer dispersions has already been disclosed wherein the polymers are non-carboxylated polymers such as natural rubber, synthetic polyisoprene (PI) or polychloroprene rubber (CR). Natural rubber contains allergenic proteins and PI and CR are of high cost
- XNBR carboxylated acrylonitrile /butadiene rubber
- the loading level of inorganic particles in common XNBR is limited, stiff or brittle films are formed due to ionic interaction between the rubber and the inorganic material.
- a particular useful group of high atomic weight elements that absorb ionising radiation comprise of heavy metals, heavy metal oxides or other heavy metal compounds. Such materials have a very high density (usually above 8 g/cm 3 ) and thus aqueous dispersions tend to sediment rapidly. This leads to an inhomogeneous distribution of inorganic particles within rubber articles. The sedimentation problem can be mitigated by use of rheology modifiers as disclosed in
- the concentration gradient results in a different ratio of polymer to inorganic material at the top and at the bottom of the container.
- quality control there is no simple way to detect differences in the concentration of the inorganic particles, an articles ability to absorb ionising radiation sufficient for its intended use cannot be judged by the thickness of the article.
- the present invention provides a polymeric/inorganic composite particle formulation, wherein the formulation includes (a) a polymer dispersion having a concentration of between 30.00 - 67.00% by dry volume, (b) a particulate inorganic material having a concentration of between 15.00 - 65.00% by dry volume, (c) a pH modifier having a concentration of between 0.30 - 3.00% by weight and (d) a dispersing agent having a concentration of between 0.25 - 5.00% by weight
- the present invention also provides a method of manufacturing a single layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a first formulation wherein, the first formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying tire former from step (a), (c) bringing the former from step (b) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (d) curing the polymeric/inorganic composite film and (e) stripping the polymeric/inorganic composite film from the former to form the single layer rubber article.
- the method includes (a) bringing a former in contact with a first formulation wherein, the first formulation
- a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 -
- step (e) bringing the former of step (d) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former from step (e) in contact with the third formulation, (g) bringing the former from step (f) in contact with the latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (h) curing the deposited films and (i) stripping the deposited films off the former to form the multi-layer rubber article.
- the present invention also provides a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying of the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposited a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration
- a method of manufacturing a multi-layer rubber article the polymeric/inorganic composite particle formulation includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 -
- step (b) drying the former from step (a), (c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former,
- the third formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight, (e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former; (f) bringing the former from step (d) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (g) curing the deposited films and (h) stripping the deposited films off the former to form the multi-layer rubber article.
- the third formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight
- the present invention also provides a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying the former from step (a), (c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 -
- Figure 1A is a cross-sectional view showing at least one layer of the polymeric/inorganic composite material of the rubber article
- Figure IB is a cross-sectional view showing at least one layer of the polymeric/inorganic composite material of the rubber article
- Figure 2A is a flow chart of the process of making thin rubber article using a polymeric/inorganic composite particle formulation
- Figure 2B is a flow chart of the process of making thin rubber article using a polymeric/inorganic composite particle formulation.
- the present invention relates to a polymeric/inorganic composite particle formulation, wherein the formulation includes (a) a polymer dispersion having a concentration of between
- the formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
- the formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
- the formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
- the formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
- the formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
- Particles in the polymer dispersion and the inorganic particles in the may be stabilised to form composite particles.
- the composite particles may move freely and do not sediment when the composite particles are agitated.
- a clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
- the formulation may be used for manufacturing rubber articles such as single layer or multi-layer thin film rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
- the polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
- the polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
- the polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex.
- the polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
- the formulation may contain a wetting agent having a concentration of up to 5% by weight and the wetting agent may be a surfactant
- the particulate inorganic material may be an ionising radiation absorbing material.
- the ionising radiation absorbing material may be a heavy metal powder.
- the ionising radiation absorbing material may be a mixture or alloy of various heavy metals.
- the ionising radiation absorbing material may be a heavy metal compound.
- the particulate inorganic material may be a magnetic material.
- the dispersing agent may be a polycarboxylic acid or polycarboxylic acid salt of molecular weight between 50,000 to 3,000, 000g/mol.
- the pH modifier may be an alkaline solution.
- the rheology modifier may be selected from xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
- the present invention also provides a method of manufacturing a single layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes the steps of (a) bringing a former in contact with a first formulation wherein, the first formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight, a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight (b) drying the former from step (a), (c) bringing the former from step (b) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (d) curing the polymeric/inorganic composite film and (e) stripping the polymeric/inorganic composite film from the former to form the single layer rubber article.
- the first formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by
- a step of drying the former from step (c) may be introduced before curing the polymeric/inorganic composite film of step (d).
- a step of beading the polymeric/inorganic composite film from step (c) may be introduced before curing the polymeric/inorganic composite film of step (d).
- a step of leaching the polymeric/inorganic composite film from step (c) may be introduced before curing the polymeric/inorganic composite film of step (d).
- the formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
- the formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
- the formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
- the formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
- the formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
- Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles.
- the composite particles may move freely and do not sediment when the composite particles are agitated.
- a clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
- the single layer rubber article is rubber articles such as gloves, tubings, condoms, arm sleeves and cover skins and catheter.
- the polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
- the polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
- the polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex.
- the polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
- the formulation may contain a wetting agent having a concentration of up to 5.00% by weight and the wetting agent may be a surfactant
- the particulate inorganic material may be an ionising radiation absorbing material
- the ionising radiation absorbing material may be a heavy metal powder.
- the ionising radiation absorbing material may be a mixture or alloy of various heavy metals.
- the ionising radiation absorbing material may be a heavy metal compound.
- the particulate inorganic material may be a magnetic material.
- the dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
- the pH modifier may be an alkaline solution.
- the rheology modifier may be selected from xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
- the wetting agent in the first formulation may be a non-ionic surfactant
- the polyvalent metal salt in the first formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
- the de-molding additive may be a stearic acid salt
- a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight; (b) drying the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation includes a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; (e) bringing the former of step (d) in contact with the
- a step of drying the former from step (c) may be introduced before bringing the former from step (c) in contact with a third formulation of step (d).
- a step of drying the former from step (d) may be introduced before bringing the former of step (d) in contact with the polymeric/inorganic composite particle formulation of step (e).
- a step of drying the former from step (e) may be introduced before bringing the former from step (e) in contact with the third formulation of step (f).
- a step of drying the former from step (f) may be introduced before bringing the former from step
- step (f) in contact with the latex formulation of step (g).
- a step of drying the former from step (g) may be introduced before curing the polymeric/inorganic composite film of step (h).
- a step of beading the polymeric/inorganic composite film from step (g) may be introduced before curing the polymeric/inorganic composite film of step (h).
- a step of leaching the polymeric/inorganic composite film from step (g) maybe introduced before curing the polymeric/inorganic composite film of step (h).
- the formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00 by weight
- the formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
- the formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
- the formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
- the formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber. Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles.
- the composite particles may move freely and do not sediment when the composite particles are agitated.
- a clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
- the multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
- the polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
- the polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
- the polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex.
- the polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
- the formulation may contain a wetting agent having a concentration of up to 5.00% by weight
- the wetting agent may be a surfactant
- the particulate inorganic material may be an ionising radiation absorbing material.
- the ionising radiation absorbing material may be a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
- the particulate inorganic material may be a magnetic material.
- the dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000 g/mol.
- the pH modifier may be an alkaline solution.
- the rheology modifier may be a xanthan gum, metiiyl cellulose, day, polyamide, polyacrylate, polyurethane or a mixture thereof.
- the wetting agent in the second formulation and third formulation may be a non-ionic surfactant
- the polyvalent metal salt in the second formulation and third formulation may be calrium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
- the de-molding additives may be a stearic add salt
- the latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styrene butadiene rubber
- PVC polyvinyl chloride
- PU polyurethane
- IIR butyl rubber
- the multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
- the outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styren
- the multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction.
- a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying of the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposited a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having
- step (h) curing the deposited films and (i) stripping the deposited films off the former to form the multi-layer rubber article.
- the deposited films on the former may be dried after step (c) is introduced but before step (d).
- a drying step may be introduced after step (d) but before step (e).
- the deposited films on the former may be dried after step (e) but before step (f).
- a drying step is introduced after step (f) but before step (g).
- the deposited films on the former may be dried after step (g) but before step (h).
- the deposited films may be beaded after step (g) but before step (h).
- the deposited films on the former may be leached after step (g) but before step (h).
- the formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
- the formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
- the formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
- the formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
- the formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
- Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles.
- the composite particles may move freely and do not sediment when the composite particles are agitated.
- a clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
- the multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
- the polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
- the polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
- the polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex
- the polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
- the formulation may contain a wetting agent having a concentration of up to 5.00% by dry rubber weight
- the wetting agent may be a surfactant
- the particulate inorganic material may be an ionising radiation absorbing material.
- the ionising radiation absorbing material may be a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
- the particulate inorganic material may be a magnetic material.
- the dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000, 000g/mol.
- the pH modifier may be an alkaline solution.
- the rheology modifier may be a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
- the wetting agent in the second formulation and third formulation may be a non-ionic surfactant
- the polyvalent metal salt in the second formulation and third formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
- the de-molding additives may be a stearic add salt
- the latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styrene butadiene rubber
- PVC polyvinyl chloride
- PU polyurethane
- IIR butyl rubber
- the multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
- the outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styren
- the multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction.
- a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00 by weight; (b) drying the former from step (a), (c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; (e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby coagul
- the former from step (c) may be repetitively brought in contact with the latex formulation for not more than 5 times before step (d), thereby coagulating the latex on the former to deposit a film of latex on the former.
- the former from step (e) may be repetitively brought in contact with the polymeric/inorganic composite particle formulation for not more than 5 times, before the multilayer rubber articled is formed, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former.
- the former from step (f) may be repetitively brought in contact with the latex formulation for not more than 5 times before step (d), thereby coagulating the latex on the former to deposit a film of latex on the former.
- the deposited films on the former may be dried after step (c).
- the deposited films on the former may be dried after step (d).
- the deposited films on the former may be dried after step (e).
- the deposited films on the former may be dried after step (f) but before step (g).
- the deposited films may be beaded after step (f] but before step (g).
- the deposited films may be leached after step (f) but before step (g).
- the formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
- the formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
- the formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
- the formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
- the formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
- Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles.
- the composite particles may move freely and do not sediment when the composite particles are agitated.
- a clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
- the multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
- the polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
- the polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
- the polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex.
- the polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
- the formulation may contain a wetting agent having a concentration of up to 5% by dry rubber weight
- the wetting agent may be a surfactant
- the particulate inorganic material may be an ionising radiation absorbing material.
- the ionising radiation absorbing material is a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
- the particulate inorganic material may be a magnetic material.
- the dispersing agent may be a polycarboxylic acid or a polycarboxytic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
- the pH modifier may be an alkaline solution.
- the rheology modifier may be a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
- the wetting agent in the second formulation and third formulation may be a non-ionic surfactant
- the polyvalent metal salt in the second formulation and third formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
- the de-molding additives may be a stearic acid salt
- the latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styrene butadiene rubber
- PVC polyvinyl chloride
- PU polyurethane
- IIR butyl rubber
- the multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
- the outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styren
- the multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction.
- a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation wherein the method includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying the former from step (a), (c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight, (e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby
- the deposited films on the former may be dried after step (c).
- a drying step may be introduced after step (d).
- the deposited films on the former may be dried after step (e).
- a drying step may be introduced after step (f).
- the deposited films on the former may be dried after step (g).
- the former from step (e) may be repeatedly brought in contact with the polymeric/inorganic composite particle formulation for not more titan 5 times before step (f), after bringing the former in contact with the third formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former.
- the former from step (g) may be repeatedly brought in contact with the latex formulation for not more than 5 times, before the multilayer rubber articled is formed, thereby coagulating the latex on the former to deposit a film of latex on the former.
- the deposited films on the former may be dried after step (g).
- the deposited films on the former may be cured after drying the deposited films on the former.
- the deposited films may be beaded after step (g).
- the deposited films may be leached after step (g).
- the formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
- the formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
- the formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
- the formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
- the formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
- Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles.
- the composite particles may move freely and do not sediment when the composite particles are agitated.
- a clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
- the multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
- the polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
- the polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
- the polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex.
- the polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
- the formulation may contain a wetting agent having a concentration of up to 5.00% by dry rubber weight
- the wetting agent may be a surfactant
- the particulate inorganic material may be an ionising radiation absorbing material
- the ionising radiation absorbing material may be a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
- the particulate inorganic material may be a magnetic material.
- the dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
- the pH modifier may be an alkaline solution.
- the rheology modifier may be a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
- the wetting agent in the second formulation and third formulation may be a non-ionic surfactant
- the polyvalent metal salt in the second formulation and third formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
- the de-molding additives is a stearic acid salt
- the latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styrene butadiene rubber
- PVC polyvinyl chloride
- PU polyurethane
- IIR butyl rubber
- the multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
- the outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styren
- the multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction.
- the present invention provides thin rubber articles ( ⁇ 0.2 mm palm thickness) that contain one or more layer of a polymeric/inorganic composite. Besides that, the present invention provides a compounding procedure to incorporate particulate inorganic materials into polymer dispersions resulting in low viscosity compounds that contain polymeric/inorganic composite particles.
- the present invention provides a dipping procedure that allows controlling the thickness of rubber articles comprising of different layers one or more of which may contain a polymeric/inorganic composite.
- the present invention provides methods for the manufacture of thin film rubber article consisting of at least two layers of controlled thickness.
- Each layer may comprise of a different base polymer such as or non-carboxylated nitrile butadiene rubber (NBR) or carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR) or carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC) or polyurethane (PU).
- NBR non-carboxylated nitrile butadiene rubber
- XNBR carboxylated nitrile butadiene rubber
- SBR non-carboxylated styrene butadiene rubber
- XSBR carboxylated styrene butadiene rubber
- PVC polyvinyl chloride
- PU polyurethan
- At least one layer contains a particulate inorganic material ⁇ comprising about 10-90% by volume (as referred as Layer 2 in Figures 1A and 1B).
- the composite layer thickness and the content of particulate inorganic material are determined by the application i.e. for detection by X-ray a lower thickness and/or content of a radiation absorbing material is required compared to radiation shielding.
- Carboxylated rubber is particular suitable for the manufacture of low dermatitis rubber articles in which the carboxylic acid functional groups serve as the primary crosslinking sites either by covalent or ionic crosslinking. Radiation shielding/detection requires such high loading of heavy metal or heavy metal oxides that the resulting ionomeric crosslinking becomes excessive, resulting in stiff or brittle films. Rubbers without carboxylation on the other hand exhibit much less interaction with these types of particulate inorganic materials but when use as the sole carrier curing additives for crosslinking are required. These curing additives can lead to Type IV allergies but without curing the filled non-carboxylated rubber would not exhibit enough physical strength that is required for a useful rubber article. It was found that by sandwiching the composite layer between layers of carboxylated rubber (support layer) an article with high content of particulate inorganic material can be made that has sufficient physical strength (Table
- Type IV allergy causative agents which is free from Type IV allergy causative agents.
- One problem that can arise from this approach is incompatibility of two different polymer types due to their differences in polarity.
- Carboxylated polymers are much more polar that natural rubber or synthetic polylsoprene for example.
- the practical issue that arise from the differences poor inter-layer adhesion which leads to delamination under normal use conditions.
- the base polymer of the composite layer needs to be compatible with support layers, so that delamination of those layers can be avoided while the article is in use.
- polychloroprene latex such as CL-750 from Showa Denko can be loaded with more than 65% (volume dry filler in dry polymer) of an Inorganic filler particles such as Bismuth Oxide (particle size d 50 approximately 1.6 ⁇ m) while maintaining sufficient adherence to the support layer (Table 1 Part I).
- Bismuth Oxide sediments rapidly so that vigorous agitation or a rheology modifier are required to ensure homogeneous distribution of the inorganic particles in the compound.
- the aforementioned mixture of chloroprene latex with Bismuth Oxide would be suitable as such for making gloves and it may contained a rheology modifier to reduce the sedimentation of the
- Bismuth particles Mechanical solutions such as agitation or pumping may also be employed to limit the sedimentation in such a way as to obtain a nearly homogeneously filled layer.
- dispersing agent polycarboxylic acid salt of molecular weight (MW) between 50
- the agglomeration step has created composite particles consisting of the inorganic material and rubber.
- AL instead of the non-agglomerated dispersion homogeneity of the composite layer is ensured since the ratio of inorganic material to polymer are determined in the preceding formulating steps, the composite layer thickness and the amount of inorganic material are directly proportional therefore.
- AL is not found to form a hard sediment layer on standing which makes it suitable for storage, continuous agitation is required during dipping. It can be advantageous to add a small quantity of a rheology modifier such as xanthan gum, methyl cellulose or clay.
- the rate of sedimentation without rheology modifier depends on the concentration of the dispersant
- the formation of a clear supernatant layer has the further advantage of preventing skinning under storage.
- the viscosity of AL without rheology modifier does not exceed 30 mPa-s which makes it suitable for continuous chain dipping (typical properties of AL as shown in Table 2).
- the article is formed, layer by layer employing a multiple dipping process.
- the initial step (Group A) is identical to conventional coagulant dipping using a coagulant formulation comprising of polyvalent metal salts, de-molding additives and wetting agents.
- the process of this invention deviates from the conventional process in that additional latex dips are performed with preceding coagulant dips (Coagulant Dips 2 and 3 in Figures 2A and 2B).
- Coagulant Dips 2 and 3 are performed using one or more auxiliary coagulant formulations comprising of wetting agent and polyvalent metal salts but without any de-molding additive whereby the polyvalent metal salt concentration is tailored to the composition of subsequent latex dip and the required layer thickness (example auxiliary coagulant formulations are shown in Table 4).
- auxiliary coagulant formulations are shown in Table 4.
- auxiliary coagulant dips By using the auxiliary coagulant dips one can easily achieve a sandwich structure of three or more layers, each of them having a defined thickness whereby it is feasible to use the same formulation for the 1 st and the 3 rd layer.
- auxiliary coagulant dips makes it particularly feasible to deposit a very thin layer of a polymeric/inorganic composite particle formulation followed by a much thicker support layer of conventional rubber.
- the absence of de-molding additive in the auxiliary coagulant formulations is important in order to prevent delamination of the individual layers of the article. Table 1. Polymeric/inorganic composite particle formulation
- M w 60000 g/mol
- Example 1 The steps of Example 1 were repeated but the formulation as shown in Table 1 was using 600 phr of the particulate inorganic material instead of 200 phr.
- the radiation polymeric/inorganic composite particle formulation that was used in example 3 was allowed to sediment and stored for 4 weeks at room temperature. The steps of Example 1 were repeated using the stored formulation after lh gentle agitation.
- Example 1 The steps of Example 1 were repeated with the exception that the auxiliary coagulant dip after L2 was omitted.
- the thickness of the individual layers of Example 1-4 is shown in Table 7. It is clear that only with the use of auxiliary coagulant a desirable distribution of the layer thickness is obtained.
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Abstract
The present invention discloses a polymeric/inorganic composite particle formulation, wherein the formulation includes a polymer dispersion having a concentration of between 30.00 - 67.00% by dry volume, inorganic particles having a concentration of between 15.00 - 65.00% by dry volume, a pH modifier having a concentration of between 0.30 - 3.00% by weight and a dispersing agent having a concentration of between 0.25 - 5.00% by weight as well as methods of producing rubber articles using the composite particle formulation.
Description
POLYMERIC/INORGANIC COMPOSITE PARTICLE FORMULATION AND METHODS OF
PRODUCING RUBBER ARTICLES USING SAID FORMULATION
FIELD OF INVENTION
The present invention relates to a formulation of polymeric/inorganic composite particles and methods of producing rubber articles using said formulation.
BACKGROUND OF INVENTION
In industries where goods are being handled using rubber articles such as gloves, the gloves themselves can become a contaminant if a glove is tom during use. Usually these contaminants are very difficult to be detected. In fields such as food or pharma, these contaminants are highly undesirable for hygiene reasons.
High atomic weight elements and their compounds have been used in rubber articles due to their intrinsic property of absorbing ionising radiation which is useful for detection by ionising radiation or ionising radiation shielding. The use of blends of particulate inorganic compounds of high atomic weight elements and aqueous polymer dispersions has already been disclosed wherein the polymers are non-carboxylated polymers such as natural rubber, synthetic polyisoprene (PI) or polychloroprene rubber (CR). Natural rubber contains allergenic proteins and PI and CR are of high cost Another much more common type of polymer for glove making is carboxylated acrylonitrile /butadiene rubber (XNBR). However, the loading level of inorganic particles in common XNBR is limited, stiff or brittle films are formed due to ionic interaction between the rubber and the inorganic material.
A particular useful group of high atomic weight elements that absorb ionising radiation comprise of heavy metals, heavy metal oxides or other heavy metal compounds. Such materials have a very high density (usually above 8 g/cm3) and thus aqueous dispersions tend to sediment rapidly. This leads to an inhomogeneous distribution of inorganic particles within rubber articles.
The sedimentation problem can be mitigated by use of rheology modifiers as disclosed in
EP1644938B1 and WO 2004/114323 A1 by WRP Asia Pacific Sdn. Bhd. However, the two aforementioned patent documents describe the use of natural rubber or pre-vulcanised natural rubber which contain allergenic proteins which requires additional steps to remove those proteins, but such removal processes are not 100% reliable. Another shortcoming in the aforementioned disclosures lies in the use of modified cellulose based rheology modifiers which lead to rather high viscosities of the resultant mixture and causes the formation of thick films in a dip coating process and it hampers the escape of entrapped air which leads to the formation of pin-holes in the rubber article. One may choose to replace natural rubber with a synthetic analogue that is otherwise free from allergenic proteins but the issues arising from high viscosity would prevail
The sedimentation problem was also addressed by mechanical means as disclosed in US5001354
(Gould). Intense agitation or re-circulation is described while the mechanical mixing is stopped just before a mold is dipped into the formulation. This approach requires a low viscosity, which is also beneficial to allow air bubbles to escape from the formulation in order to prevent pin-hole defects. But due to high density of the dispersed tungsten particles (19.3 g/cm3) sedimentation produces a concentration gradient of the heavy metal particles in the formulation within seconds.
Due to the nature of such blends, the concentration gradient results in a different ratio of polymer to inorganic material at the top and at the bottom of the container. In terms of quality control, there is no simple way to detect differences in the concentration of the inorganic particles, an articles ability to absorb ionising radiation sufficient for its intended use cannot be judged by the thickness of the article.
Therefore, there is a need for a new formulation using high density inorganic particles and also methods of producing rubber articles using said formulation.
SUMMARY OF INVENTION
Accordingly, the present invention provides a polymeric/inorganic composite particle formulation, wherein the formulation includes (a) a polymer dispersion having a concentration of between 30.00 - 67.00% by dry volume, (b) a particulate inorganic material having a concentration of between 15.00 - 65.00% by dry volume, (c) a pH modifier having a concentration of between 0.30 - 3.00% by weight and (d) a dispersing agent having a concentration of between 0.25 - 5.00% by weight
Further, the present invention also provides a method of manufacturing a single layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a first formulation wherein, the first formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying tire former from step (a), (c) bringing the former from step (b) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (d) curing the polymeric/inorganic composite film and (e) stripping the polymeric/inorganic composite film from the former to form the single layer rubber article.
Also provided is a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation
wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 -
2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight, (e) bringing the former of step (d) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former from step (e) in contact with the third formulation, (g) bringing the former from step (f) in contact with the latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (h) curing the deposited films and (i) stripping the deposited films off the former to form the multi-layer rubber article. Besides that; the present invention also provides a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying of the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposited a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration
0.10 - 30.00% by weight, (e) bringing the former from step (d) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former from step (e) in contact with the third formulation, (g) bringing the former from step (f) in contact with the latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former,
(h) curing the deposited films and (i) stripping the deposited films off the former to form the multi-layer rubber article.
Further, there is provided a method of manufacturing a multi-layer rubber article the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 -
5.00 by weight, (b) drying the former from step (a), (c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former,
(d) bringing the former in contact with a third formulation wherein, the third formulation. includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight, (e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former; (f) bringing the former from step (d) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (g) curing the deposited films and (h) stripping the deposited films off the former to form the multi-layer rubber article.
Last but not least, the present invention also provides a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying the former from step (a), (c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 -
2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight, (e) bringing the former in contact with the polymeric/inorganic composite particle formulation,
thereby coagulating the polymeric/inorganic composite partide formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former in contact with the third formulation, (g) bringing the former from step (f) In contact with a latex formulation, thereby magulating the latex on the former to deposit a film of latex on the former, (h) curing the deposited films and 0) stripping the deposited films off the former to form the multi-layer rubber article.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1A is a cross-sectional view showing at least one layer of the polymeric/inorganic composite material of the rubber article;
Figure IB is a cross-sectional view showing at least one layer of the polymeric/inorganic composite material of the rubber article;
Figure 2A is a flow chart of the process of making thin rubber article using a polymeric/inorganic composite particle formulation; and
Figure 2B is a flow chart of the process of making thin rubber article using a polymeric/inorganic composite particle formulation.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Broadly, the present invention relates to a polymeric/inorganic composite particle formulation, wherein the formulation includes (a) a polymer dispersion having a concentration of between
30.00 - 67.00% by dry volume, (b) a particulate inorganic material having a concentration of between 15.00 - 65.00% by dry volume, (c) a pH modifier having a concentration of between 0.30
- 3.00% by weight and (d) a dispersing agent having a concentration of between 0.25 - 5.00% by weight
The formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight The formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
The formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
The formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber. The formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
Particles in the polymer dispersion and the inorganic particles in the may be stabilised to form composite particles. The composite particles may move freely and do not sediment when the composite particles are agitated. A clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
The formulation may be used for manufacturing rubber articles such as single layer or multi-layer thin film rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
The polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
The polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber. The polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex.
The polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
The formulation may contain a wetting agent having a concentration of up to 5% by weight and the wetting agent may be a surfactant
The particulate inorganic material may be an ionising radiation absorbing material. The ionising radiation absorbing material may be a heavy metal powder. The ionising radiation absorbing material may be a mixture or alloy of various heavy metals. The ionising radiation absorbing material may be a heavy metal compound.
The particulate inorganic material may be a magnetic material.
The dispersing agent may be a polycarboxylic acid or polycarboxylic acid salt of molecular weight between 50,000 to 3,000, 000g/mol.
The pH modifier may be an alkaline solution.
The rheology modifier may be selected from xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
Further, the present invention also provides a method of manufacturing a single layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes the steps of (a) bringing a former in contact with a first formulation wherein, the first formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight, a
polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight (b) drying the former from step (a), (c) bringing the former from step (b) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (d) curing the polymeric/inorganic composite film and (e) stripping the polymeric/inorganic composite film from the former to form the single layer rubber article.
A step of drying the former from step (c) may be introduced before curing the polymeric/inorganic composite film of step (d). A step of beading the polymeric/inorganic composite film from step (c) may be introduced before curing the polymeric/inorganic composite film of step (d).
A step of leaching the polymeric/inorganic composite film from step (c) may be introduced before curing the polymeric/inorganic composite film of step (d).
The formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
The formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
The formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
The formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
The formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles. The composite particles may move freely and do not sediment when the composite particles are agitated. A clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated. The single layer rubber article is rubber articles such as gloves, tubings, condoms, arm sleeves and cover skins and catheter.
The polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
The polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber. The polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex. The polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
The formulation may contain a wetting agent having a concentration of up to 5.00% by weight and the wetting agent may be a surfactant The particulate inorganic material may be an ionising radiation absorbing material The ionising radiation absorbing material may be a heavy metal powder. The ionising radiation absorbing material may be a mixture or alloy of various heavy metals. The ionising radiation absorbing material may be a heavy metal compound.
The particulate inorganic material may be a magnetic material. The dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
The pH modifier may be an alkaline solution.
The rheology modifier may be selected from xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
The wetting agent in the first formulation may be a non-ionic surfactant
The polyvalent metal salt in the first formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
The de-molding additive may be a stearic acid salt
Also provided is a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight; (b) drying the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation includes a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; (e) bringing the former of step (d) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former from step (e) in contact with the third formulation, (g) bringing the former from step (f) in contact with the latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (h) curing the deposited films and (i) stripping the deposited films off the former to form the multi-layer rubber article.
A step of drying the former from step (c) may be introduced before bringing the former from step (c) in contact with a third formulation of step (d).
A step of drying the former from step (d) may be introduced before bringing the former of step (d) in contact with the polymeric/inorganic composite particle formulation of step (e).
A step of drying the former from step (e) may be introduced before bringing the former from step (e) in contact with the third formulation of step (f). A step of drying the former from step (f) may be introduced before bringing the former from step
(f) in contact with the latex formulation of step (g).
A step of drying the former from step (g) may be introduced before curing the polymeric/inorganic composite film of step (h).
A step of beading the polymeric/inorganic composite film from step (g) may be introduced before curing the polymeric/inorganic composite film of step (h).
A step of leaching the polymeric/inorganic composite film from step (g) maybe introduced before curing the polymeric/inorganic composite film of step (h).
The formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00 by weight The formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
The formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
The formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber. The formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles.
The composite particles may move freely and do not sediment when the composite particles are agitated. A clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
The multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
The polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber. The polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber. The polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex. The polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
The formulation may contain a wetting agent having a concentration of up to 5.00% by weight The wetting agent may be a surfactant
The particulate inorganic material may be an ionising radiation absorbing material. The ionising radiation absorbing material may be a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
The particulate inorganic material may be a magnetic material. The dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000 g/mol.
The pH modifier may be an alkaline solution.
The rheology modifier may be a xanthan gum, metiiyl cellulose, day, polyamide, polyacrylate, polyurethane or a mixture thereof.
The wetting agent in the second formulation and third formulation may be a non-ionic surfactant
The polyvalent metal salt in the second formulation and third formulation may be calrium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
The de-molding additives may be a stearic add salt
The latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer. The outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction. Further, there is also provided a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a
concentration 0.10 - 5.00% by weight, (b) drying of the former from step (a), (c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposited a film of latex on the former, (d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration
0.10 - 30.00% by weight, (e) bringing the former from step (d) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former from step (e) in contact with the third formulation, (g) bringing the former from step (f) in contact with the latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former,
(h) curing the deposited films and (i) stripping the deposited films off the former to form the multi-layer rubber article. The deposited films on the former may be dried after step (c) is introduced but before step (d).
A drying step may be introduced after step (d) but before step (e).
The deposited films on the former may be dried after step (e) but before step (f).
A drying step is introduced after step (f) but before step (g).
The deposited films on the former may be dried after step (g) but before step (h). The deposited films may be beaded after step (g) but before step (h).
The deposited films on the former may be leached after step (g) but before step (h).
The formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
The formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
The formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
The formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
The formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber. Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles. The composite particles may move freely and do not sediment when the composite particles are agitated. A clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
The multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
The polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber. The polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber. The polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex
The polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
The formulation may contain a wetting agent having a concentration of up to 5.00% by dry rubber weight
The wetting agent may be a surfactant
The particulate inorganic material may be an ionising radiation absorbing material. The ionising radiation absorbing material may be a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
The particulate inorganic material may be a magnetic material.
The dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000, 000g/mol.
The pH modifier may be an alkaline solution. The rheology modifier may be a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
The wetting agent in the second formulation and third formulation may be a non-ionic surfactant The polyvalent metal salt in the second formulation and third formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
The de-molding additives may be a stearic add salt
The latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer. The outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction.
Also provided is a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation, wherein the method includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00 by weight; (b) drying the former from step (a), (c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by
weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; (e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former from step (d) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (g) curing the deposited films and (h) stripping the deposited films off the former to form the multi-layer rubber article.
The former from step (c) may be repetitively brought in contact with the latex formulation for not more than 5 times before step (d), thereby coagulating the latex on the former to deposit a film of latex on the former.
The former from step (e) may be repetitively brought in contact with the polymeric/inorganic composite particle formulation for not more than 5 times, before the multilayer rubber articled is formed, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former.
The former from step (f) may be repetitively brought in contact with the latex formulation for not more than 5 times before step (d), thereby coagulating the latex on the former to deposit a film of latex on the former.
The deposited films on the former may be dried after step (c).
The deposited films on the former may be dried after step (d).
The deposited films on the former may be dried after step (e).
The deposited films on the former may be dried after step (f) but before step (g).
The deposited films may be beaded after step (f] but before step (g). The deposited films may be leached after step (f) but before step (g).
The formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight The formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
The formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber. The formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
The formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles. The composite particles may move freely and do not sediment when the composite particles are agitated. A clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
The multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
The polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber. The polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber. The polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex. The polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
The formulation may contain a wetting agent having a concentration of up to 5% by dry rubber weight
The wetting agent may be a surfactant
The particulate inorganic material may be an ionising radiation absorbing material. The ionising radiation absorbing material is a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
The particulate inorganic material may be a magnetic material.
The dispersing agent may be a polycarboxylic acid or a polycarboxytic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
The pH modifier may be an alkaline solution.
The rheology modifier may be a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
The wetting agent in the second formulation and third formulation may be a non-ionic surfactant
The polyvalent metal salt in the second formulation and third formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
The de-molding additives may be a stearic acid salt
The latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer. The outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction.
There is also provided a method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation wherein the method includes the steps of (a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight, (b) drying the former from step (a), (c) bringing the former
in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight, (e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former, (f) bringing the former in contact with the third formulation, (g) bringing the former from step (f) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former, (h) curing the deposited films and (i) stripping the deposited films off the former to form the multi-layer rubber article.
The deposited films on the former may be dried after step (c). A drying step may be introduced after step (d).
The deposited films on the former may be dried after step (e).
A drying step may be introduced after step (f).
The deposited films on the former may be dried after step (g).
The former from step (e) may be repeatedly brought in contact with the polymeric/inorganic composite particle formulation for not more titan 5 times before step (f), after bringing the former in contact with the third formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former.
The former from step (g) may be repeatedly brought in contact with the latex formulation for not more than 5 times, before the multilayer rubber articled is formed, thereby coagulating the latex on the former to deposit a film of latex on the former. The deposited films on the former may be dried after step (g).
The deposited films on the former may be cured after drying the deposited films on the former.
The deposited films may be beaded after step (g).
The deposited films may be leached after step (g).
The formulation may contain a rheology modifier having a concentration of between 0.15 - 2.00% by weight
The formulation may contain sulphur having a concentration of up to 5.00% of dry weight rubber.
The formulation may contain a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
The formulation may contain zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
The formulation may contain an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
Particles in the polymer dispersion and the particulate inorganic material may be stabilised to form composite particles. The composite particles may move freely and do not sediment when the composite particles are agitated. A clear or translucent supernatant layer may be formed above a sediment of composite particles when not agitated.
The multi-layer rubber article may be rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
The polymer dispersion may be a carboxylated latex of acrylonitrile-butadiene rubber or styrene- butadiene rubber or polychloroprene rubber.
The polymer dispersion may be a non-carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber. The polymer dispersion may be a natural rubber latex or a pre-vulcanised natural rubber latex.
The polymer dispersion may be a synthetic polyisoprene latex or a polyurethane dispersion.
The formulation may contain a wetting agent having a concentration of up to 5.00% by dry rubber weight
The wetting agent may be a surfactant
The particulate inorganic material may be an ionising radiation absorbing material
The ionising radiation absorbing material may be a heavy metal powder or a mixture or alloy of different heavy metals or a heavy metal compound.
The particulate inorganic material may be a magnetic material.
The dispersing agent may be a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
The pH modifier may be an alkaline solution.
The rheology modifier may be a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
The wetting agent in the second formulation and third formulation may be a non-ionic surfactant
The polyvalent metal salt in the second formulation and third formulation may be calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
The de-molding additives is a stearic acid salt
The latex formulation may be one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multi-layer rubber article may be a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer. The outer layer and the inner layer may be made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR),
carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
The multilayer rubber article may be chlorinated or having its inner layer surface coated to reduce friction.
The present invention will now be described in more specific details.
Specifically, the present invention provides thin rubber articles (≤ 0.2 mm palm thickness) that contain one or more layer of a polymeric/inorganic composite. Besides that, the present invention provides a compounding procedure to incorporate particulate inorganic materials into polymer dispersions resulting in low viscosity compounds that contain polymeric/inorganic composite particles.
The present invention provides a dipping procedure that allows controlling the thickness of rubber articles comprising of different layers one or more of which may contain a polymeric/inorganic composite.
The present invention provides methods for the manufacture of thin film rubber article consisting of at least two layers of controlled thickness. Each layer may comprise of a different base polymer such as or non-carboxylated nitrile butadiene rubber (NBR) or carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR) or carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC) or polyurethane (PU). At least one layer (composite layer) contains a particulate inorganic material · comprising about 10-90% by volume (as referred as Layer 2 in Figures 1A and 1B). The composite layer thickness and the content of particulate inorganic material are determined by the application i.e. for detection by X-ray a lower thickness and/or content of a radiation absorbing material is required compared to radiation shielding.
The degree of radiation absorption depends on the concentration of high atomic weight elements. the layer thickness, the density and the atomic weight (higher = better).
Carboxylated rubber is particular suitable for the manufacture of low dermatitis rubber articles in which the carboxylic acid functional groups serve as the primary crosslinking sites either by covalent or ionic crosslinking. Radiation shielding/detection requires such high loading of heavy metal or heavy metal oxides that the resulting ionomeric crosslinking becomes excessive, resulting in stiff or brittle films. Rubbers without carboxylation on the other hand exhibit much less interaction with these types of particulate inorganic materials but when use as the sole carrier curing additives for crosslinking are required. These curing additives can lead to Type IV allergies but without curing the filled non-carboxylated rubber would not exhibit enough physical strength that is required for a useful rubber article. It was found that by sandwiching the composite layer between layers of carboxylated rubber (support layer) an article with high content of particulate inorganic material can be made that has sufficient physical strength (Table
1) which is free from Type IV allergy causative agents. One problem that can arise from this approach is incompatibility of two different polymer types due to their differences in polarity.
Carboxylated polymers are much more polar that natural rubber or synthetic polylsoprene for example. The practical issue that arise from the differences poor inter-layer adhesion which leads to delamination under normal use conditions. The base polymer of the composite layer needs to be compatible with support layers, so that delamination of those layers can be avoided while the article is in use.
It was found that polychloroprene latex such as CL-750 from Showa Denko can be loaded with more than 65% (volume dry filler in dry polymer) of an Inorganic filler particles such as Bismuth Oxide (particle size d50 approximately 1.6 μm) while maintaining sufficient adherence to the support layer (Table 1 Part I). However, the Bismuth Oxide sediments rapidly so that vigorous agitation or a rheology modifier are required to ensure homogeneous distribution of the inorganic particles in the compound.
The aforementioned mixture of chloroprene latex with Bismuth Oxide would be suitable as such for making gloves and it may contained a rheology modifier to reduce the sedimentation of the
Bismuth particles. Mechanical solutions such as agitation or pumping may also be employed to limit the sedimentation in such a way as to obtain a nearly homogeneously filled layer. The addition of dispersing agent; polycarboxylic acid salt of molecular weight (MW) between 50
000 to 3 000000 g/mol to the formulation as shown in Table 1 Part I leads to co-agglomeration of the inorganic particles and polychloroprene rubber particles forming an agglomerated latex
(AL) (Table 1 Part II). This is a surprising result as the polymer particles, the inorganic particles as well as the dispersant are of anionic character. At a pH greater than 7 the agglomeration is independent of the nature of inorganic material, it can be shown that ordinary sulphur powder
(particle size: 30 μm), zinc oxide powder (particle size: 1 μm, white seal) or titanium dioxide
(particle size: 300 nm) will form a dispersions of composite particles (Table 3). These examples demonstrate the general applicability of the method in terms of the nature of the particulate inorganic material. It can also be shown that the agglomeration can be achieved with various anionically stabilised polymer dispersions such as polychloroprene latex, carboxylated acrylonitrile/butadiene latex etc. Carboxylated polymer dispersions can principally be used to produce AL, however, depending on the concentration of the inorganic particles and the degree of carboxylation the resultant film will exhibit greater stiffness than films made with non- carboxylated polymers. Generally, below pH 7 coagulation predominates, composite particles of irregular shape and size are formed.
While AL still sediments it does so with the formation of a clear supernatant layer and the sediment has a homogeneous visual appearance throughout The agglomeration step has created composite particles consisting of the inorganic material and rubber. By using AL instead of the non-agglomerated dispersion homogeneity of the composite layer is ensured since the ratio of inorganic material to polymer are determined in the preceding formulating steps, the composite layer thickness and the amount of inorganic material are directly proportional therefore. AL is
not found to form a hard sediment layer on standing which makes it suitable for storage, continuous agitation is required during dipping. It can be advantageous to add a small quantity of a rheology modifier such as xanthan gum, methyl cellulose or clay. It was also found that the rate of sedimentation without rheology modifier depends on the concentration of the dispersant The formation of a clear supernatant layer has the further advantage of preventing skinning under storage. The viscosity of AL without rheology modifier does not exceed 30 mPa-s which makes it suitable for continuous chain dipping (typical properties of AL as shown in Table 2).
As shown in Figures 2A and 2B, the article is formed, layer by layer employing a multiple dipping process. The initial step (Group A) is identical to conventional coagulant dipping using a coagulant formulation comprising of polyvalent metal salts, de-molding additives and wetting agents. The process of this invention deviates from the conventional process in that additional latex dips are performed with preceding coagulant dips (Coagulant Dips 2 and 3 in Figures 2A and 2B). The
Coagulant Dips 2 and 3, are performed using one or more auxiliary coagulant formulations comprising of wetting agent and polyvalent metal salts but without any de-molding additive whereby the polyvalent metal salt concentration is tailored to the composition of subsequent latex dip and the required layer thickness (example auxiliary coagulant formulations are shown in Table 4). After reaching the last step in Group B as shown in Figure 2A and 2B, additional layers can be built up by repeating the steps of Group B multiple times. Drying and leaching steps in each Group (A, B, C and D) are optional. By using the auxiliary coagulant dips one can easily achieve a sandwich structure of three or more layers, each of them having a defined thickness whereby it is feasible to use the same formulation for the 1st and the 3rd layer. Using auxiliary coagulant dips makes it particularly feasible to deposit a very thin layer of a polymeric/inorganic composite particle formulation followed by a much thicker support layer of conventional rubber. The absence of de-molding additive in the auxiliary coagulant formulations is important in order to prevent delamination of the individual layers of the article.
Table 1. Polymeric/inorganic composite particle formulation
Table 2. Typical properties of a dispersion with polymeric/inorganic composite particles
Table 3. Example inorganic materials that form composite particles, the amount is adjusted for constant volume fraction
Example 1
L1: A ceramic glove former is cleaned, dried and coated with a standard coagulant formulation
(14% Calcium Nitrate) and then dried at 70°C The dry coated former is then dipped into a standard XNBR compound (total solid compound: 15%, pH: 10.0) with a total contact time of 7 seconds to form a 1st layer. The former with the 1st layer is then dried for 1 minute at 90°C, leached for 10 seconds in water at 60°C and dried for 60 seconds at 35°C.
L2: The dry former with layer LI is then dipped into the 1st auxiliary coagulant formulation (Table
4, with Teric 320 as the wetting agent) with a total contact time of 14 seconds. The former is then dried at 70°C for 5 minutes and subsequently dipped into a polymeric/inorganic composite particle formulation as shown in Table 1 (using CL-750 as the non-carboxylated latex, sodium dodecylbenzene sulfonate as the wetting agent, Bismuth Oxide as the particulate inorganic material, no rheology modifier and Acumer 1510 from Dow Chemicals as the dispersing agent,
Mw = 60000 g/mol) with a total contact time of 7 seconds to deposit the 2nd layer, followed by drying at 90°C for 1 minute, leaching for 10 seconds in water at 60°C and drying for 60 seconds at35«C.
L3: The dry former with layers L1+L3 is then dipped into the 2nd auxiliary coagulant formulation (Table 4) with a total contact time of 14 seconds. The former is then dried at 70°C for 5 minutes and subsequently dipped into the same standard XNBR compound that was used for Layer LI with a total contact time of 7 seconds to deposit the 3rd layer. The former with the three layers is then dried at 90°C for 1 minute and leached for 2 minutes at 60°C. After leaching the 3-layer film is beaded and dried at 90°C for 5 minutes and finally cured at 120°C for 20 minutes. After curing the glove is stripped off the former. The thickness of each layer is assessed at samples which have subsequent layers L2+L3 or L3 omitted.
Table 4. Auxiliary coagulant formulations 1 + 2 (based on 100 parts dry coagulant)
Example 2
The steps of Example 1 were repeated but the formulation as shown in Table 1 was using 600 phr of the particulate inorganic material instead of 200 phr.
The physical properties of examples 1 and 2 are shown in table 6.
Example 3
The radiation polymeric/inorganic composite particle formulation that was used in example 3 was allowed to sediment and stored for 4 weeks at room temperature. The steps of Example 1 were repeated using the stored formulation after lh gentle agitation.
The attenuation results of examples 1-3 are shown in Table 5.
Example 4
The steps of Example 1 were repeated with the exception that the auxiliary coagulant dip after L2 was omitted.
The thickness of the individual layers of Example 1-4 is shown in Table 7. It is clear that only with the use of auxiliary coagulant a desirable distribution of the layer thickness is obtained.
Table 5. Thickness and attenuation results of Examples 1-3
Table 6. Physical Properties of a Rubber Article that contains a polymeric/inorganic composite layer
Claims
1. A polymeric/inorganic composite particle formulation, wherein the formulation includes: a) a polymer dispersion having a concentration of between 30.00 - 67.00% by dry volume; b) inorganic particles having a concentration of between 15.00 - 65.00% by dry volume; c) a pH modifier having a concentration of between 0.30 - 3.00% by weight; and d) a dispersing agent having a concentration of between 0.25 - 5.00% by weight
2. The formulation as claimed in Claim 1, wherein the formulation contains a rheology modifier having a concentration of between 0.15 - 2.00% by weight
3. The formulation as claimed in Claim 1, wherein the formulation contains sulphur having a concentration of up to 5.00% of dry weight rubber.
4. The formulation as claimed in Claim 1, wherein the formulation contains a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
5. The formulation as claimed in Claim 1, wherein the formulation contains zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
6. The formulation as claimed in Claim 1, wherein the formulation contains an anti- degradant with a concentration of up to 5.00% of dry weight rubber.
7. The formulation as claimed in Claim 1, wherein particles in the polymer dispersion and particles of inorganic material are stabilised to form composite particles.
8. The formulation as claimed in Claim 7, wherein the composite particles move freely and do not sediment when the composite particles are agitated.
9. The formulation as claimed in Claim 7, wherein the composite particles form a clear or translucent supernatant layer when the composite particles are not agitated.
10. The formulation as claimed in claim 9, wherein the clear or translucent supernatant layer is formed above a sediment of composite particles when not agitated.
11. The formulation as claimed in any one of Claims 1 to 10, wherein the formulation is used for manufacturing rubber articles.
12. The formulation as claimed in Claim 11, wherein the rubber articles are single layer or multi-layer thin film rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
13. The formulation as claimed in Claim 1, wherein the polymer dispersion is a carboxyiated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber.
14. The formulation as claimed in Claim 1, wherein the polymer dispersion is a non- carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
15. The formulation as claimed in Claim 1, wherein the polymer dispersion is a natural rubber latex or a pre- vulcanised natural rubber latex.
16. The formulation as claimed in Claim 1, wherein the polymer dispersion is a synthetic polyisoprene latex or a polyurethane dispersion.
17. The formulation as claimed in Claim 1, wherein the formulation contains a wetting agent having a concentration of up to 5% by weight
18. The formulation as claimed in Claim 17, wherein the wetting agent is a surfactant
19. The formulation as claimed in Claim 1, wherein the particulate inorganic material is an ionising radiation absorbing material.
20. The formulation as claimed in Claim 19, wherein the ionising radiation absorbing material is a heavy metal powder.
21. The formulation as claimed in Claim 19, wherein the ionising radiation absorbing material is a mixture or alloy of various heavy metals.
22. The formulation as claimed in Claim 19, wherein the ionising radiation absorbing material is a heavy metal compound.
23. The formulation as claimed in Claim 1, wherein the particulate inorganic material is a magnetic material.
24. The formulation as claimed in Claim 1, wherein the dispersing agent is a polycarboxylic acid or polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
25. The formulation as claimed in Claim 1, wherein the pH modifier is an alkaline solution.
26. The formulation as claimed in Claim 2, wherein the rheology modifier is selected from xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
27. A method of manufacturing a single layer rubber article from tire polymeric/inorganic composite particle formulation as claimed in any one of Claims 1 - 26, wherein the method includes the steps of: a) bringing a former in contact with a first formulation wherein, the first formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight, a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a demolding additive having a concentration 0.10 - 5.00% by weight; b) drying the former from step (a); c) bringing the former from step (b) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on die former to deposit a polymeric/inorganic composite film on the former; d) curing the deposited polymeric/inorganic composite film; and e) stripping the polymeric/inorganic composite film from the former to form the single layer rubber article.
28. The method as claimed in Claim 27, wherein a step of drying the former from step (c) is introduced before curing the polymeric/inorganic composite film of step (d).
29. The method as claimed in Claim 27, wherein a step of beading the polymeric/inorganic composite film from step (c) is introduced before curing the polymeric/inorganic composite film of step (d).
30. The method as claimed in Claim 27, wherein a step of leaching the polymeric/inorganic composite film from step (c) is introduced before curing the polymeric/inorganic composite film of step (d).
31. The method as claimed in Claim 27, wherein the formulation contains a rheology modifier having a concentration of between 0.15 - 2.00% by weight
32. The method as claimed in Claim 27, wherein the formulation contains sulphur having a concentration of up to 5.00% of dry weight rubber.
33. The method as claimed in Claim 27, wherein the formulation contains a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
34. The method as claimed in Claim 27, wherein the formulation contains zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
35. The method as claimed in Claim 27, wherein the formulation contains an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
36. The method as claimed in Claim 27, wherein particles in the polymer dispersion and particles of the inorganic material are stabilised to form composite particles.
37. The method as claimed in Claim 36, wherein the composite particles move freely and do not sediment when the composite particles are agitated.
38. The method as claimed in Claim 36, wherein the composite particles form a clear or translucent supernatant layer when the composite particles are not agitated.
39. The method as claimed in Claim 38, wherein the clear or translucent supernatant layer is formed above a sediment of composite particles when not agitated.
40. The method as claimed in any one of Claims 27 to 39, wherein the single layer rubber article is rubber articles such as gloves, tubings, condoms, arm sleeves and cover skins and catheter.
41. The method as claimed in Claim 27, wherein the polymer dispersion is a carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber.
42. The method as claimed in to Claim 27, wherein the polymer dispersion is a non- carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
43. The method as claimed in Claim 27, wherein the polymer dispersion is a natural rubber latex or a pre-vulcanised natural rubber latex.
44. The method as claimed in Claim 27, wherein the polymer dispersion is a synthetic polyisoprene latex or a polyurethane dispersion.
45. The method as claimed in Claim 27, wherein the formulation contains a wetting agent having a concentration of up to 5.00% by weight
46. The method as claimed in Claim 45, wherein the wetting agent is a surfactant
47. The method as claimed in Claim 27, wherein the particulate inorganic material is an ionising radiation absorbing material.
48. The method as claimed in Claim 47, wherein the ionising radiation absorbing material is a heavy metal powder.
49. The method as claimed in Claim 47, wherein the ionising radiation absorbing material is a mixture or alloy of various heavy metals.
50. The method as claimed in Claim 47, wherein the ionising radiation absorbing material is a heavy metal compound.
51. The method as claimed in Claim 27, wherein the particulate inorganic material is a magnetic material.
52. The method as claimed in Claim 27, wherein the dispersing agent is a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000g/mol.
53. The method as claimed in Claim 27, wherein the pH modifier is an alkaline solution.
54. The method as claimed in Claim 27, wherein the rheology modifier is selected from xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
55. The method as claimed in Claim 27, wherein the wetting agent in the first formulation is a non-ionic surfactant
56. The method as claimed in Claim 27, wherein the polyvalent metal salt in the first formulation is calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
57. The method as claimed in Claim 27, wherein the de-molding additive is a stearic acid salt
58. A method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation as claimed in any one of Claims 1 - 26, wherein the method includes the steps of: a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight; b) drying the former from step (a); c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former; d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation includes a wetting agent having a concentration between 0.10 -
2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; e) bringing the former of step (d) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former; f) bringing the former from step (e) in contact with the third formulation; g) bringing the former from step (f) in contact with the latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former; h) curing the deposited films; and i) stripping the deposited films off the former to form the multi-layer rubber article.
59. The method as claimed in Claim 58, wherein a step of drying the former from step (c) is introduced before bringing the former from step (c) in contact with a third formulation of step (d).
60. The method as claimed in Claim 58, wherein a step of drying the former from step (d) is introduced before bringing the former of step (d) in contact with the polymeric/inorganic composite particle formulation of step (e).
61. The method as claimed in Claim 58, wherein a step of drying the former from step (e) is introduced before bringing the former from step (e) in contact with the third formulation of step (f).
62. The method as claimed in Claim 58, wherein a step of drying the former from step (f) is introduced before bringing the former from step (f) in contact with the latex formulation of step (g).
63. The method as claimed in Claim 58, wherein a step of drying the former from step (g) is introduced before curing the polymeric/inorganic composite film of step (h).
64. The method as claimed in Claim 58, wherein a step of beading the polymeric/inorganic composite film from step (g) is introduced before curing the polymeric/inorganic composite film of step (h).
65. The method as claimed in Claim 58, wherein a step of leaching the polymeric/inorganic composite film from step (g) is introduced before curing the polymeric/inorganic composite film of step (h).
66. The method as claimed in Claim 58, wherein the formulation contains a rheology modifier having a concentration of between 0.15 - 2.00 by weight
67. The method as claimed in Claim 58, wherein the formulation contains sulphur having a concentration of up to 5.00% of dry weight rubber.
68. The method as claimed in Claim 58, wherein the formulation contains a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
69. The method as claimed in Claim 58, wherein the formulation contains zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
70. The method as claimed in Claim 58, wherein the formulation contains an anti-degradant with a concentration of up to 5.00% of dry weight rubber.
71. The method as claimed in Claim 58, wherein particles in the polymer dispersion and particles of the inorganic material are stabilised to form composite particles.
72. The method as claimed in Claim 71, wherein the composite particles move freely and do not sediment when the composite particles are agitated.
73. The method as claimed in Claim 71, wherein the composite particles form a clear or translucent supernatant layer when the composite particles are not agitated.
74. The method as claimed in claim 73, wherein the clear or translucent supernatant layer is formed above a sediment of composite particles when not agitated.
75. The method as claimed in any one of Claims 58 to 74, wherein the multi-layer rubber article is rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
76. The method as claimed in Claim 58, wherein the polymer dispersion is a carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber.
77. The method as claimed in to Claim 58, wherein the polymer dispersion is a non- carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
78. The method as claimed in Claim 58, wherein the polymer dispersion is a natural rubber latex or a pre-vulcanised natural rubber latex.
79. The method as claimed in Claim 58, wherein the polymer dispersion is a synthetic polyisoprene latex or a polyurethane dispersion.
80. The method as claimed in Claim 58, wherein the formulation contains a wetting agent having a concentration of up to 5.00% by weight
81. The method as claimed in Claim 80, wherein the wetting agent is a surfactant
82. The method as claimed in Claim 58, wherein the particulate inorganic material is an ionising radiation absorbing material.
83. The method as claimed in Claim 82, wherein the ionising radiation absorbing material is a heavy metal powder.
84. The method as claimed in Claim 82, wherein the ionising radiation absorbing material is a mixture or alloy of different heavy metals.
85. The method as claimed in Claim 82, wherein the ionising radiation absorbing material is a heavy metal compound.
86. The method as claimed in Claim 58, wherein the particulate inorganic material is a magnetic material.
87. The method as claimed in Claim 58, wherein the dispersing agent is a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to 3,000,000 g/mol.
88. The method as claimed in Claim 58, wherein the pH modifier is an alkaline solution.
89. The method as claimed in Claim 58, wherein the rheology modifier is a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
90. The method as claimed in Claim 58, wherein the wetting agent in the second formulation and third formulation is a non-ionic surfactant
91. The method as claimed in Claim 58, wherein the polyvalent metal salt in the second formulation and third formulation is calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
92. The method as claimed in Claim 58, wherein the de-molding additives is a stearic acid salt
93. The method as claimed in Claim 58, wherein the latex formulation is one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene
butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
94. The method as claimed in Claim 58, wherein the multi-layer rubber article is a 3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
95. The method as claimed in Claim 94, wherein the outer layer and the inner layer are made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber
(NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
96. The method as claimed in Claim 94 wherein the multilayer rubber article is chlorinated or having its inner layer surface coated to reduce friction.
97. A method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation as claimed in any one Claim 1 - 26, wherein the method includes the steps of: a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight; b) drying of the former from step (a); c) bringing the former from step (b) in contact with a latex formulation, thereby coagulating the latex on the former to deposited a film of latex on the former; d) bringing the former from step (c) in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 -
2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; e) bringing the former from step (d) in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former; f) bringing the former from step (e) in contact with the third formulation; g) bringing the former from step (f) in contact with the latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former; h) curing the deposited films; and i) stripping the deposited films off the former to form the multi-layer rubber article.
98. The method as claimed in Claim 97, wherein the deposited films on the former are dried after step (c) is introduced but before step (d).
99. The method as claimed in Claim 97, wherein a drying step is introduced after step (d) but before step (e).
100. The method as claimed in Claim 97, wherein the deposited films on the former are dried after step (e) but before step (f).
101. The method as claimed in Claim 97, wherein a drying step is introduced after step
(f) but before step (g).
102. The method as claimed in Claim 97, wherein the deposited films on the former are dried after step (g) but before step (h).
103. The method as claimed in Claim 97, wherein the deposited films are beaded after step (g) but before step (h).
104. The method as claimed in Claim 97, wherein the deposited films on the former are leached after step (g) but before step (h).
105. The method as claimed in Claim 97, wherein the formulation contains a rheology modifier having a concentration of between 0.15 - 2.00% by weight
106. The method as claimed in Claim 97, wherein the formulation contains sulphur having a concentration of up to 5.00% of dry weight rubber.
107. The method as claimed in Claim 97, wherein the formulation contains a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
108. The method as claimed in Claim 97, wherein the formulation contains zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
109. The method as claimed in Claim 97, wherein the formulation contains an anti- degradant with a concentration of up to 5.00% of dry weight rubber.
110. The method as claimed in Claim 97, wherein particles in the polymer dispersion and particles of the inorganic material are stabilised to form composite particles.
111. The method as claimed in Claim 110, wherein the composite particles move freely and do not sediment when the composite particles are agitated.
112. The method as claimed in Claim 110, wherein the composite particles form a clear or translucent supernatant layer when the composite particles are not agitated.
113. The method as claimed in claim 112, wherein the clear or translucent supernatant layer is formed above a sediment of composite particles when not agitated.
114. The method as claimed in any one of Claims 97 to 113, wherein the multi-layer rubber article is rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
115. The method as claimed in Claim 97, wherein the polymer dispersion is a carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber.
116. The method as claimed in to Claim 97, wherein the polymer dispersion is a non- carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
117. The method as claimed in Claim 97, wherein the polymer dispersion is a natural rubber latex or a pre-vulcanised natural rubber latex.
118. The method as claimed in Claim 97, wherein the polymer dispersion is a synthetic polyisoprene latex or a polyurethane dispersion.
119. The method as claimed in Claim 97, wherein the formulation contains a wetting agent having a concentration of up to 5.00% by dry rubber weight
120. The method as claimed in Claim 119, wherein the wetting agent is a surfactant
121. The method as claimed in Claim 97, wherein the particulate inorganic material is an ionising radiation absorbing material.
122. The method as claimed in Claim 121, wherein the ionising radiation absorbing material is a heavy metal powder.
123. The method as claimed in Claim 121, wherein the ionising radiation absorbing material is a mixture or alloy of different heavy metals.
124. The method as claimed in Claim 121, wherein the ionising radiation absorbing material is a heavy metal compound.
125. The method as claimed in Claim 97, wherein the particulate inorganic material is a magnetic material
126. The method as claimed in Claim 97, wherein the dispersing agent is a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to
3,000,000g/mol.
127. The method as claimed in Claim 97, wherein the pH modifier is an alkaline solution.
128. The method as claimed in Claim 97, wherein the rheology modifier is a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
129. The method as claimed in Claim 97, wherein the wetting agent in the second formulation and third formulation is a non-ionic surfactant
130. The method as claimed in Claim 97, wherein the polyvalent metal salt in the second formulation and third formulation is calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
131. The method as claimed in Claim 97, wherein the de-molding additives is a stearic acid salt
132. The method as claimed in Claim 97, wherein the latex formulation is one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
133. The method as claimed in Claim 97, wherein the multi-layer rubber article is a 3- layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
134. The method as claimed in Claim 133, wherein the outer layer and the inner layer are made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
135. The method as claimed in Claim 133 wherein the multilayer rubber article is chlorinated or having its inner layer surface coated to reduce friction.
136. A method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation as claimed in any one of Claims 1 -
26, wherein the method includes the steps of: a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00 by weight; b) drying the former from step (a); c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former; d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former; f) bringing the former from step (d) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former; g) curing the deposited films; and h) stripping the deposited films off the former to form the multi-layer rubber article.
137. The method as claimed in Claim 136, wherein the former from step (c) is repetitively brought in contact with the latex formulation for not more than 5 times before step (d), thereby coagulating the latex on the former to deposit a film of latex on the former.
138. The method as claimed in Claim 136, wherein the former from step (e) is repetitively brought in contact with the polymeric/inorganic composite particle formulation for not more than 5 times, before the multilayer rubber articled is formed, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former.
139. The method as claimed in Claim 136, wherein the former from step (f) is repetitively brought in contact with the latex formulation for not more than 5 times before step (d), thereby coagulating the latex on the former to deposit a film of latex on the former.
140. The method as claimed in Claim 136, wherein the deposited films on the former are dried after step (c).
141. The method as claimed in Claim 136, wherein the deposited films on the former are dried after step (d).
142. The method as claimed in Claim 136, wherein the deposited films on the former are dried after step (e).
143. The method as claimed in Claim 136, wherein the deposited films on the former are dried after step (f) but before step (g).
144. The method as claimed in Claim 136, wherein the deposited films are beaded after step (f) but before step (g).
145. The method as claimed in Claim 136, wherein the deposited films are leached after step (f) but before step (g).
146. The method as claimed in Claim 136, wherein the formulation contains a theology modifier having a concentration of between 0.15 - 2.00% by weight
147. The method as claimed in Claim 136, wherein the formulation contains sulphur having a concentration of up to 5.00% of dry weight rubber.
148. The method as claimed in Claim 136, wherein the formulation contains a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
149. The method as claimed in Claim 136, wherein the formulation contains zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
150. The method as claimed in Claim 136, wherein the formulation contains an anti- degradant with a concentration of up to 5.00% of dry weight rubber.
151. The method as claimed in Claim 136, wherein particles in the polymer dispersion and particles of the inorganic material are stabilised to form composite particles.
152. The method as claimed in Claim 151, wherein the composite particles move freely and do not sediment when the composite particles are agitated.
153. The method as claimed in Claim 151, wherein the composite particles form a clear or translucent supernatant layer when the composite particles are not agitated.
154. The method as claimed in claim 151, wherein the clear or translucent supernatant layer is formed above a sediment of composite particles when not agitated.
155. The method as claimed in any one of Claims 136 to 154, wherein the multi-layer rubber article is rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
156. The method as claimed in Claim 136, wherein the polymer dispersion is a carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber.
157. The method as claimed in to Claim 136, wherein the polymer dispersion is a non- carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
158. The method as claimed in Claim 136, wherein the polymer dispersion is a natural rubber latex or a pre-vulcanised natural rubber latex.
159. The method as claimed in Claim 136, wherein the polymer dispersion is a synthetic polyisoprene latex or a polyurethane dispersion.
160. The method as claimed in Claim 136, wherein the formulation contains a wetting agent having a concentration of up to 5% by dry rubber weight
161. The method as claimed in Claim 160, wherein the wetting agent is a surfactant
162. The method as claimed in Claim 136, wherein the particulate inorganic material is an ionising radiation absorbing material.
163. The method as claimed in Claim 162, wherein the ionising radiation absorbing material is a heavy metal powder.
164. The method as claimed in Claim 162, wherein the ionising radiation absorbing material is a mixture or alloy of different heavy metals.
165. The method as claimed in Claim 162, wherein the ionising radiation absorbing material is a heavy metal compound.
166. The method as claimed in Claim 136, wherein the particulate inorganic material is a magnetic material.
167. The method as claimed in Claim 136, wherein the dispersing agent is a polycarboxyiic acid or a polycarboxylic acid salt of molecular weight between 50,000 to
3,000,000g/mol.
168. The method as claimed in Claim 136, wherein the pH modifier is an alkaline solution.
169. The method as claimed in Claim 136, wherein the rheology modifier is a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
170. The method as claimed in Claim 136, wherein the wetting agent in the second formulation and third formulation is a non-ionic surfactant
171. The method as claimed in Claim 136, wherein the polyvalent metal salt in the second formulation and third formulation is calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
172. The method as claimed in Claim 136, wherein the de-molding additives is a stearic acid salt
173. The method as claimed in Claim 136, wherein the latex formulation is one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
174. The method as claimed in Claim 136, wherein the multi-layer rubber article is a
3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
175. The method as claimed in Claim 174, wherein the outer layer and the inner layer are made from a polymer dispersion selected from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
176. The method as claimed in Claim 173 wherein the multilayer rubber article is chlorinated or having its inner layer surface coated to reduce friction.
177. A method of manufacturing a multi-layer rubber article from the polymeric/inorganic composite particle formulation as claimed in any one of Claims 1 -
26, wherein the method includes the steps of: a) bringing a former in contact with a second formulation wherein, the second formulation includes, a wetting agent having a concentration between 0.10 - 2.00% by weight; a polyvalent metal salt having a concentration 0.50 - 30.00% by weight and a de-molding additive having a concentration 0.10 - 5.00% by weight; b) drying the former from step (a); c) bringing the former in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former; d) bringing the former in contact with a third formulation wherein, the third formulation, includes, a wetting agent having a concentration between 0.10 - 2.00% by weight and a polyvalent metal salt having a concentration 0.10 - 30.00% by weight; e) bringing the former in contact with the polymeric/inorganic composite particle formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former; f) bringing the former in contact with the third formulation; g) bringing the former from step (f) in contact with a latex formulation, thereby coagulating the latex on the former to deposit a film of latex on the former; h) curing the deposited films; and i) stripping the deposited films off the former to form the multi-layer rubber article.
178. The method as claimed in Claim 177, wherein the deposited films on the former are dried after step (c).
179. The method as claimed in Claim 177, wherein a drying step is introduced after step (d).
180. The method as claimed in Claim 177, wherein the deposited films on the former are dried after step (e).
181. The method as claimed in Claim 177, wherein a drying step is introduced after step [f).
182. The method as claimed in Claim 177, wherein the deposited films on the former are dried after step (g).
183. The method as claimed in Claim 177, wherein the former from step (e) is repeatedly brought in contact with the polymeric/inorganic composite particle formulation for not more than 5 times before step (f), after bringing the former in contact with the third formulation, thereby coagulating the polymeric/inorganic composite particle formulation on the former to deposit a polymeric/inorganic composite film on the former.
184. The method as claimed in Claim 177, wherein the former from step (g) is repeatedly brought in contact with the latex formulation for not more than 5 times, before the multilayer rubber articled is formed, thereby coagulating the latex on the former to deposit a film of latex on the former.
185. The method as claimed in Claim 177, wherein the deposited films on the former are dried after step (g).
186. The method as claimed in Claim 177, wherein the deposited films on the former are cured after drying tire deposited films on the former.
187. The method as claimed in Claim 177, wherein the deposited films are beaded after step (g).
188. The method as claimed in Claim 177, wherein the deposited films are leached after step (g).
189. The method as claimed in Claim 177, wherein the formulation contains a rheology modifier having a concentration of between 0.15 - 2.00% by weight
190. The method as claimed in Claim 177, wherein the formulation contains sulphur having a concentration of up to 5.00% of dry weight rubber.
191. The method as claimed in Claim 177, wherein the formulation contains a vulcanisation accelerator having a concentration of up to 2.00% of dry weight rubber.
192. The method as claimed in Claim 177, wherein the formulation contains zinc oxide having a concentration of up to 1040.00% of dry weight rubber.
193. The method as claimed in Claim 177, wherein the formulation contains an anti- degradant with a concentration of up to 5.00% of dry weight rubber.
194. The method as claimed in Claim 177, wherein particles in the polymer dispersion and particles of the particulate inorganic material are stabilised to form composite particles.
195. The method as claimed in Claim 194, wherein the composite particles move freely and do not sediment when the composite particles are agitated.
196. The method as claimed in Claim 194, wherein the composite particles form a clear or translucent supernatant layer when the composite particles are not agitated.
197. The method as claimed in Claim 196, wherein the clear or translucent supernatant layer is formed above a sediment of composite particles when not agitated.
198. The method as claimed in any one of Claims 177 to 197, wherein the multi-layer rubber article is rubber articles such as gloves, tubings, condoms, arm sleeves, cover skins and catheters.
199. The method as claimed in Claim 177, wherein the polymer dispersion is a carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber.
200. The method as claimed in to Claim 177, wherein the polymer dispersion is a non- carboxylated latex of acrylonitrile-butadiene rubber or styrene-butadiene rubber or polychloroprene rubber or butyl rubber.
201. The method as claimed in Claim 177, wherein the polymer dispersion is a natural rubber latex or a pre-vulcanised natural rubber latex.
202. The method as claimed in Claim 177, wherein the polymer dispersion is a synthetic polyisoprene latex or a polyurethane dispersion.
203. The method as claimed in Claim 177, wherein the formulation contains a wetting agent having a concentration of up to 5.00% by dry rubber weight
204. The method as claimed in Claim 203, wherein the wetting agent is a surfactant
205. The method as daimed in Claim 177, wherein the particulate inorganic material is an ionising radiation absorbing material.
206. The method as claimed in Claim 205, wherein the ionising radiation absorbing material is a heavy metal powder.
207. The method as claimed in Claim 205, wherein the ionising radiation absorbing material is a mixture or alloy of different heavy metals.
208. The method as daimed in Claim 205, wherein the ionising radiation absorbing material is a heavy metal compound.
209. The method as daimed in Claim 177, wherein the particulate inorganic material is a magnetic material.
210. The method as daimed in Claim 177, wherein the dispersing agent is a polycarboxylic acid or a polycarboxylic acid salt of molecular weight between 50,000 to
3,000,000g/mol
211. The method as claimed in Claim 177, wherein the pH modifier is an alkaline solution.
212. The method as claimed in Claim 177, wherein the rheology modifier is a xanthan gum, methyl cellulose, clay, polyamide, polyacrylate, polyurethane or a mixture thereof.
213. The method as claimed in Claim 177, wherein the wetting agent in the second formulation and third formulation is a non-ionic surfactant
214. The method as claimed in Claim 177, wherein the polyvalent metal salt in the second formulation and third formulation is calcium chloride, calcium nitrate, aluminium chloride or aluminium nitrate or a mixture thereof.
215. The method as claimed in Claim 177, wherein the de-molding additives is a stearic acid salt
216. The method as claimed in Claim 177, wherein the latex formulation is one latex dispersion from non-carboxylated nitrile butadiene rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
217. The method as claimed in Claim 177, wherein the multi-layer rubber article is a
3-layer rubber article comprising of an outer layer, an intermediary layer and an internal layer.
218. The method as claimed in Claim 217, wherein the outer layer and the inner layer are made from a polymer dispersion selected from non-carboxylated nitrile butadiene
rubber (NBR), carboxylated nitrile butadiene rubber (XNBR), non-carboxylated styrene butadiene rubber (SBR), carboxylated styrene butadiene rubber (XSBR), polychloroprene, polyisoprene, polyvinyl chloride (PVC), polyurethane (PU), butyl rubber (IIR) or a mixture thereof.
219. The method as claimed in Claim 217 wherein the multilayer rubber article is chlorinated or having its inner layer surface coated to reduce friction.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2022526443A JP7234463B2 (en) | 2019-11-07 | 2020-07-27 | Polymer/Inorganic Composite Particle Blends Used to Make Rubber Articles in Dip Coating Processes and Methods of Making Rubber Articles Using the Blends |
EP20884362.3A EP4055092A4 (en) | 2019-11-07 | 2020-07-27 | Polymeric/inorganic composite particle formulation and methods of producing rubber articles using said formulation |
Applications Claiming Priority (2)
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MYPI2019006533A MY198073A (en) | 2019-11-07 | 2019-11-07 | Polymeric/inorganic composite particle formulation and methods of producing rubber articles using said formulation |
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WO2021091366A1 true WO2021091366A1 (en) | 2021-05-14 |
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EP (1) | EP4055092A4 (en) |
JP (1) | JP7234463B2 (en) |
MY (1) | MY198073A (en) |
WO (1) | WO2021091366A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115093511A (en) * | 2022-07-14 | 2022-09-23 | 星宇新材料股份有限公司 | Butyronitrile butadiene styrene composite latex for dipped gloves and preparation method and application thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0615534B1 (en) * | 1991-12-03 | 1997-04-16 | Rohm And Haas Company | Aqueous dispersion of composite particles including polymeric latex |
US20050031870A1 (en) * | 2003-04-03 | 2005-02-10 | China Petroleum & Chemical Corporation | Composite powder, preparation and use thereof |
WO2007078038A1 (en) * | 2005-12-30 | 2007-07-12 | Cheil Industries Inc. | Thermoplastic nanocomposite resin composite materials |
CN102050972A (en) * | 2009-10-27 | 2011-05-11 | 中国石油化工股份有限公司 | Modified rubber composition and preparation method thereof |
US20170015819A1 (en) * | 2014-02-28 | 2017-01-19 | Midori Anzen Co., Ltd | Glove and glove composition |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001123306A (en) | 1999-10-22 | 2001-05-08 | Seikoh Chem Co Ltd | Nbr gloves and method for producing the same |
EP1563000A1 (en) * | 2002-11-11 | 2005-08-17 | WRP Asia Pacific Sdn. Bhd. | A synthetic latex composition |
EP2088362A1 (en) * | 2006-10-25 | 2009-08-12 | Osaka Prefectural Government | Outdoor illuminating device and illuminating method |
WO2010098008A1 (en) | 2009-02-28 | 2010-09-02 | 日本ゼオン株式会社 | Composition for dip forming, and dip-formed articles |
JP5575254B2 (en) * | 2009-12-01 | 2014-08-20 | コッサン エスディーエヌ ビーエイチディー | Elastomer rubber and rubber products that do not use crosslinking accelerators and sulfur |
KR101832875B1 (en) * | 2010-09-30 | 2018-04-13 | 코싼 에스디엔 비에이치디 | Elastomer rubber and elastomer product that do not use vulcanization accelerator or sulfur |
US9637621B2 (en) | 2013-09-30 | 2017-05-02 | Zeon Corporation | Dip-forming composition and dip-formed article |
-
2019
- 2019-11-07 MY MYPI2019006533A patent/MY198073A/en unknown
-
2020
- 2020-07-27 JP JP2022526443A patent/JP7234463B2/en active Active
- 2020-07-27 EP EP20884362.3A patent/EP4055092A4/en active Pending
- 2020-07-27 WO PCT/MY2020/000008 patent/WO2021091366A1/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0615534B1 (en) * | 1991-12-03 | 1997-04-16 | Rohm And Haas Company | Aqueous dispersion of composite particles including polymeric latex |
US20050031870A1 (en) * | 2003-04-03 | 2005-02-10 | China Petroleum & Chemical Corporation | Composite powder, preparation and use thereof |
WO2007078038A1 (en) * | 2005-12-30 | 2007-07-12 | Cheil Industries Inc. | Thermoplastic nanocomposite resin composite materials |
CN102050972A (en) * | 2009-10-27 | 2011-05-11 | 中国石油化工股份有限公司 | Modified rubber composition and preparation method thereof |
US20170015819A1 (en) * | 2014-02-28 | 2017-01-19 | Midori Anzen Co., Ltd | Glove and glove composition |
Non-Patent Citations (1)
Title |
---|
See also references of EP4055092A4 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115093511A (en) * | 2022-07-14 | 2022-09-23 | 星宇新材料股份有限公司 | Butyronitrile butadiene styrene composite latex for dipped gloves and preparation method and application thereof |
CN115093511B (en) * | 2022-07-14 | 2022-11-01 | 星宇新材料股份有限公司 | Butyronitrile butadiene styrene composite latex for dipped gloves and preparation method and application thereof |
Also Published As
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EP4055092A1 (en) | 2022-09-14 |
JP2023500155A (en) | 2023-01-04 |
MY198073A (en) | 2023-07-31 |
EP4055092A4 (en) | 2023-12-06 |
JP7234463B2 (en) | 2023-03-07 |
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