WO2020044228A1 - Holding material and method of manufacturing same, and pollution control apparatus - Google Patents
Holding material and method of manufacturing same, and pollution control apparatus Download PDFInfo
- Publication number
- WO2020044228A1 WO2020044228A1 PCT/IB2019/057200 IB2019057200W WO2020044228A1 WO 2020044228 A1 WO2020044228 A1 WO 2020044228A1 IB 2019057200 W IB2019057200 W IB 2019057200W WO 2020044228 A1 WO2020044228 A1 WO 2020044228A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- region
- holding material
- main body
- body portion
- pollution control
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims abstract description 134
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 19
- 239000012784 inorganic fiber Substances 0.000 claims abstract description 43
- 238000004804 winding Methods 0.000 claims abstract description 19
- 230000002093 peripheral effect Effects 0.000 claims abstract description 10
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 8
- 239000011147 inorganic material Substances 0.000 claims abstract description 8
- 239000011230 binding agent Substances 0.000 claims description 13
- 239000010954 inorganic particle Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 239000000853 adhesive Substances 0.000 claims description 7
- 230000001070 adhesive effect Effects 0.000 claims description 7
- 238000009751 slip forming Methods 0.000 claims 2
- 230000000873 masking effect Effects 0.000 description 23
- 239000000835 fiber Substances 0.000 description 18
- 239000007788 liquid Substances 0.000 description 14
- 239000002245 particle Substances 0.000 description 9
- 230000003068 static effect Effects 0.000 description 9
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- 239000011347 resin Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
- 239000000919 ceramic Substances 0.000 description 6
- 239000010419 fine particle Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 229910001220 stainless steel Inorganic materials 0.000 description 5
- 239000010935 stainless steel Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- -1 alkali metal salts Chemical class 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 238000005755 formation reaction Methods 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
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- 150000004706 metal oxides Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
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- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 238000004873 anchoring Methods 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000001965 increasing effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 229920001290 polyvinyl ester Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 229920006337 unsaturated polyester resin Polymers 0.000 description 2
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- 101100451301 Caenorhabditis elegans mls-2 gene Proteins 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 238000003917 TEM image Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 229910052915 alkaline earth metal silicate Inorganic materials 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000007766 curtain coating Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- GVALZJMUIHGIMD-UHFFFAOYSA-H magnesium phosphate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O GVALZJMUIHGIMD-UHFFFAOYSA-H 0.000 description 1
- 239000004137 magnesium phosphate Substances 0.000 description 1
- 229910000157 magnesium phosphate Inorganic materials 0.000 description 1
- 229960002261 magnesium phosphate Drugs 0.000 description 1
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000009816 wet lamination Methods 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
- F01N3/10—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
- F01N3/24—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by constructional aspects of converting apparatus
- F01N3/28—Construction of catalytic reactors
- F01N3/2839—Arrangements for mounting catalyst support in housing, e.g. with means for compensating thermal expansion or vibration
- F01N3/2853—Arrangements for mounting catalyst support in housing, e.g. with means for compensating thermal expansion or vibration using mats or gaskets between catalyst body and housing
- F01N3/286—Arrangements for mounting catalyst support in housing, e.g. with means for compensating thermal expansion or vibration using mats or gaskets between catalyst body and housing the mats or gaskets having corrugations or cavities
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01N—GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
- F01N3/00—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
- F01N3/08—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
- F01N3/10—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
- F01N3/24—Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by constructional aspects of converting apparatus
- F01N3/28—Construction of catalytic reactors
- F01N3/2839—Arrangements for mounting catalyst support in housing, e.g. with means for compensating thermal expansion or vibration
- F01N3/2853—Arrangements for mounting catalyst support in housing, e.g. with means for compensating thermal expansion or vibration using mats or gaskets between catalyst body and housing
- F01N3/2864—Arrangements for mounting catalyst support in housing, e.g. with means for compensating thermal expansion or vibration using mats or gaskets between catalyst body and housing the mats or gaskets comprising two or more insulation layers
Definitions
- Exhaust gas from an automobile engine includes carbon monoxide (CO), hydrocarbon (HC), nitrogen oxide (NOx), and the like. Exhaust gases discharged from a diesel engine also include particulate matters such as soot. As means for removing these, an exhaust gas cleaning system using a ceramic catalytic converter or a diesel particulate filter (DPF) is known.
- CO carbon monoxide
- HC hydrocarbon
- NOx nitrogen oxide
- DPF diesel particulate filter
- An object of the present disclosure is to provide a holding material including a surface that is easy to be wound around an outer peripheral surface of a pollution control element at the manufacturing step of a pollution control apparatus, and that can improve holding force.
- an object of the present disclosure is to provide a method of manufacturing a holding material and a pollution control apparatus including a holding material.
- FIG. 6 is a cross-sectional view schematically illustrating an apparatus for measuring a coefficient of static friction of a holding material.
- the first region where at least the inorganic material is attached improves a coefficient of static friction or impart adhesiveness, and thus can contribute to improvement of holding force. Furthermore, for example, even when the first region is harder as compared to the second region, since the first region and the second region are interleaved with each other in the winding direction, the ease of winding around an outer peripheral surface of a pollution control element can be maintained sufficiently.
- the holding material 10 includes, for example, a convex portion lOa at one end and a concave portion lOb at the other end, is formed in a shape such that the convex portion lOa and the concave portion lOb mate with each other when the holding material 10 is wound around the pollution control element 30.
- the shape and the like of the mating are not particularly limited, and other forms such as an F-shape can be used.
- the main body portion 1 is obtained by mixing inorganic fibers and an organic binder as starting materials with any additives, and then continuously performing the steps such as spreading the inorganic fibers, preparing a slurry, molding by papermaking, and mold pressing.
- the second inorganic fiber may have a different aspect ratio from the first inorganic fiber constituting the main body portion 1.
- the aspect ratio of the second inorganic fiber may be, for example, approximately 60 to approximately 2000, and may be approximately 100 to
- An inorganic fiber having an aspect ratio of approximately 60 or greater has a tendency to be capable of suppressing scattering of the fiber pieces as compared to an inorganic fiber having a smaller aspect ratio at the time of manufacturing a pollution control apparatus.
- an inorganic fiber having an aspect ratio of approximately 2000 or less is more readily available as compared to an inorganic fiber having a larger aspect ratio.
- JP 2017-210815 For the inorganic fiber, reference can be made to the specification of JP 2017-210815.
- the mat obtained at step (a) can be dried at step (b).
- the mat obtained at step (a) may be dried in a hot air drier set to approximately 80 to approximately 250°C for approximately 10 to approximately 180 minutes.
- the amount of application per unit area (solid mass) in the first region Rl may be, for example, approximately 1 to approximately 50 g/m 2 , or approximately 2 to approximately 40 g/m 2 , or approximately 5 to approximately 30 g/m 2 .
- Moisture may be volatilized by performing the drying step after application.
- the main body portion 1 to which the liquid is applied to form a pattern may be dried for approximately 10 to approximately 180 minutes in a hot air drier set to approximately 80 to approximately 250°C.
- the first region Rl is formed on the surface of the main body portion 1.
- the step of forming the first region Rl may be performed in multiple steps. Namely, a method of forming the first region Rl may include the steps of applying a liquid containing the first material to the entire surface of the main body portion 1, masking a region corresponding to the second region R2, and applying a liquid containing the first material to a region corresponding to the first region Rl in this order. Alternatively, the method of forming the first region Rl may include the steps of masking a region corresponding to the second region R2, applying a liquid containing the first material to a region corresponding to the first region Rl, removing the mask covering the region corresponding to the second region R2, and applying a liquid containing the first material to the entire surface of the main body portion 1 in this order.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Exhaust Gas After Treatment (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
A holding material including a surface that is easy to be wound around an outer peripheral surface of a pollution control element at the manufacturing step of a pollution control apparatus and that can improve holding force. The holding material including, a main body portion having a sheet-like shape and including at least a first inorganic fiber, a first region provided on at least one surface of the main body portion and where a first material including at least an inorganic material is attached to the first inorganic fiber, and a part in which, along a winding direction of the main body portion, the first region and a second region are interleaved with each other, and the first region is not attached to the second region or is attached to the second region with fewer attachment amount than to the first region.
Description
HOLDING MATERIAL AND METHOD OF MANUFACTURING SAME, AND POLLUTION
CONTROL APPARATUS
TECHNICAL FIELD
The present disclosure relates to a holding material and a method of manufacturing the same, and a pollution control apparatus.
BACKGROUND ART
Exhaust gas from an automobile engine includes carbon monoxide (CO), hydrocarbon (HC), nitrogen oxide (NOx), and the like. Exhaust gases discharged from a diesel engine also include particulate matters such as soot. As means for removing these, an exhaust gas cleaning system using a ceramic catalytic converter or a diesel particulate filter (DPF) is known.
Furthermore, installation of a gasoline particulate filter (GPF) has also been studied. These devices are commonly referred to as pollution control apparatuses.
In general, a pollution control apparatus (for example, a ceramic catalytic converter) comprises a pollution control element (for example, a honeycomb-shaped ceramic catalyst support), a metal casing that houses the pollution control element, and a holding material that fills a gap between an outer peripheral surface of the pollution control element and an inside surface of the casing. The holding material holds the pollution control element within the casing and prevents a mechanical shock due to an impact, vibration, and the like from inadvertently being applied to the pollution control element. The holding material prevents movement and destruction of the pollution control element within the casing and provides a desirable effect in the operation lifetime of the pollution control element. This type of holding material is also commonly referred to as a mounting material. These holding materials are normally in the form of a mat made of a single layer or a plurality of layers, and are used by winding around a pollution control element.
Patent JP 10-337480 A discloses a catalytic converter comprising a monolith on which a catalyst is supported, a casing housing the monolith, and a holding material interposed in a gap between the monolith and the casing, wherein a large number of grooves orthogonal to a winding direction of the holding material are provided on a surface of the holding material on the side that is in contact with the monolith. According to Patent JP 10-337480 A, a large number of the grooves on a specific surface of the holding material are provided, the holding material can be wound easily on the monolith and the adhesion of the holding material to the monolith can be further enhanced (see 0037 of Patent JP 10-337480 A). Patent JP 2007-332922 A discloses a holding sealant including a groove-shaped structure on a specific surface. Patent JP 2017-31869 A discloses a holding sealant including a surface on which lattice-like grooves are formed.
SUMMARY OF INVENTION
An object of the present disclosure is to provide a holding material including a surface that is easy to be wound around an outer peripheral surface of a pollution control element at the manufacturing step of a pollution control apparatus, and that can improve holding force.
Furthermore, an object of the present disclosure is to provide a method of manufacturing a holding material and a pollution control apparatus including a holding material.
A holding material according to the present disclosure is a holding material wound on an outer peripheral (e.g., circumferential, oval, etc.) surface of a pollution control element, the holding material including, a main body portion having a sheet-like shape and including at least a first inorganic fiber, a first region provided on at least one surface of the main body portion and where a first material including at least an inorganic material is attached to the first inorganic fiber, and a part in which, along a winding direction of the main body portion, the first region and a second region are interleaved with each other, and the first region is not attached to the second region or is attached to the second region with fewer attachment amount than to the first region.
A pollution control apparatus according to one aspect of the present disclosure includes a casing, a pollution control element disposed within the casing, and the holding material disposed between the casing and the pollution control element.
A method of manufacturing a holding material according to one aspect of the present disclosure includes the steps of preparing a main body portion of a holding material, and providing a first region on at least one surface of the main body portion.
According to the present disclosure, provided is a holding material including a surface that is easy to be wound around an outer peripheral surface of a pollution control element at the manufacturing step of a pollution control apparatus and that can improve holding force.
Furthermore, according to the present disclosure, a method of manufacturing a holding material and a pollution control apparatus including a holding material are provided.
BRIEF DESCRIPTION OF DRAWINGS
FIG. 1 is a perspective view illustrating an embodiment of a holding material according to the present disclosure.
FIG. 2 is a schematic cross-sectional view along line II-II in FIG. 1.
FIG. 3 is a cross-sectional view schematically illustrating an embodiment of a pollution control apparatus according to the present disclosure.
FIGS. 4A to 4C are top views each illustrating another embodiment of a holding material.
FIGS. 5 A to 5 C are top views each illustrating another embodiment of a holding material.
FIG. 6 is a cross-sectional view schematically illustrating an apparatus for measuring a coefficient of static friction of a holding material.
DESCRIPTION OF EMBODIMENTS
The holding material according to the present disclosure is a holding material wound on an outer peripheral (e.g., circumferential) surface of a pollution control element, the holding material including, a main body portion having a sheet-like shape and including at least a first inorganic fiber, a first region provided on at least one surface of the main body portion and where a first material including at least an inorganic material is attached to the first inorganic fiber, and a part in which, along a winding direction of the main body portion, the first region and a second region are interleaved with each other, and the first region is not attached to the second region or is attached to the second region with fewer attachment amount than to the first region. According to the holding material according to the present embodiment, the first region where at least the inorganic material is attached improves a coefficient of static friction or impart adhesiveness, and thus can contribute to improvement of holding force. Furthermore, for example, even when the first region is harder as compared to the second region, since the first region and the second region are interleaved with each other in the winding direction, the ease of winding around an outer peripheral surface of a pollution control element can be maintained sufficiently.
Detailed description of embodiments of the present disclosure will be given below with reference to the drawings.
FIG. 1 is a perspective view illustrating an example of a holding material. FIG. 2 is a schematic cross-sectional view along line II-II in FIG. 1. The holding material 10 is for winding around a pollution control element 30 having a shape of a cylinder or elliptical column and holding the pollution control element 30 in a casing 20 (see FIG. 3). The holding material 10 has a length corresponding to a length of an outer periphery of the pollution control element 30. The holding material 10 includes, for example, a convex portion lOa at one end and a concave portion lOb at the other end, is formed in a shape such that the convex portion lOa and the concave portion lOb mate with each other when the holding material 10 is wound around the pollution control element 30. Note that the shape and the like of the mating are not particularly limited, and other forms such as an F-shape can be used.
The holding material 10 includes a main body portion 1 having a sheet-like shape, a first region Rl provided on a surface Fl of the main body portion 1, and a second region R2 between two first regions Rl . The main body portion 1 having a sheet-like shape includes at least a first inorganic fiber. The first region Rl is a region where the first material adheres to the first inorganic fibers constituting the main body portion 1. The second region is a region where the first material is not attached or is attached with fewer attachment amount than the first region Rl . The first region Rl and the second region R2 are present interleaved with each other along the winding direction of the main body portion 1 (a direction of arrow A as illustrated in FIG. 1).
In the present embodiment, as illustrated in FIG. 1, the first region Rl is formed to make a striped pattern. Namely, the first region Rl is formed to make a regular pattern in the surface Fl,
and both the first region Rl and the second region R2 are formed continuously from one end to the other end in the width direction of the main body portion 1 (a direction orthogonal to the direction of arrow A). The width and pitch of the stripes may be set appropriately according to the size of the holding material 10 or flexibility required for the holding material. According to the study of the present inventors, when the first region Rl is stripe-shaped, an area proportion of the first region Rl based on the area of the surface Fl may be, for example, 15 to 90%, or 15 to 80%, or 20 to 70%.
The main body portion 1 mainly includes an inorganic fiber (first inorganic fiber). The thickness of the main body portion 1 is, for example, approximately 5 to approximately 15 mm. Specific examples of the inorganic fiber constituting the main body portion 1 include glass fibers, ceramic fibers, carbon fibers, silicon carbide fibers, and boron fibers, and other inorganic fibers may be used as necessary. One type of the inorganic fiber selected from the above may be used alone, or a combination of two or more types thereof may be used, or a composite fiber thereof may be used. Among these, particularly preferred are ceramic fibers such as alumina fibers, silica fibers, and alumina-silica fibers. The ceramic fibers may be used alone, or a combination of two or more types thereof may be used, or composite fibers thereof may be used.
The main body portion 1 is obtained by mixing inorganic fibers and an organic binder as starting materials with any additives, and then continuously performing the steps such as spreading the inorganic fibers, preparing a slurry, molding by papermaking, and mold pressing. WO
2004/061279 and US 6051193 can be referred to for details of a wet method (wet lamination method). Note that the type of the organic binder and the amount of the organic binder used are not particularly limited. For example, acrylic resins, styrene -butadiene resins, acrylonitrile resins, polyurethane resins, natural rubbers, polyvinyl acetate resins, and the like provided in the form of latex can be used as the organic binder. Alternatively, a flexible thermoplastic resin such as an unsaturated polyester resin, an epoxy resin, and a polyvinyl ester resin may be used as the organic binder.
The first region Rl is a region where the first material is attached to the inorganic fiber of the main body portion 1. The unit area amount of the first material present in the first region Rl may be, for example, 1 to 50 g/m2, 2 to 40 g/m2, or 5 to 30 g/m2. The amount of the first material in the first region Rl may be set as appropriate in accordance with the size of a coefficient of static friction or adhesiveness required of the holding material 10. The first material includes at least an inorganic material. Examples of the inorganic material include inorganic particles, inorganic fibers (second inorganic fibers), and inorganic adhesives. One type of these materials may be used alone, or two or more types thereof may be used in combination.
Examples of inorganic particles include metal oxide, nitride, and carbide particles.
Preferred examples of metal oxide having heat resistance include, but are not limited to, silica, alumina, mullite, zirconia, magnesia, and titania. Examples of other suitable materials may include
boron nitride and boron carbide. One type of the particles made from these materials may be used alone, or two or more types thereof may be used in combination.
The inorganic particles can be used with a variety of particle sizes in response to the type of inorganic material and a desired friction improving effect. It is usually preferred that the inorganic particles have an average particle size of approximately 1 to 100 nm. When the average particle size of the inorganic particles is 1 nm or greater, a friction increasing effect is exhibited.
On the other hand, when the average particle size of the inorganic particles is less than or equal to 100 nm, a friction increasing effect is exhibited, and the peeling off of the inorganic particles from the main body portion 1 can be suppressed sufficiently. The average particle size of the inorganic particles is more preferably within the range of approximately 10 to 80 nm, and more preferably in the range of approximately 20 to 50 nm. For the inorganic particles (inorganic colloidal particles), reference can be made to WO 2007/030410.
Examples of an inorganic fiber (second inorganic fiber) include metal oxide, nitride, and carbide fibers. The diameter of the inorganic fiber may be approximately 1 nm to approximately 15 nm, and for example, may be approximately 1 nm or greater, approximately 2 nm or greater, or approximately 3 nm or greater, and approximately 15 nm or less, approximately 8 nm or less, or approximately 5 nm or less. An inorganic fiber having a diameter of approximately 1 nm or greater is advantageous in that the inorganic fiber is more readily available as compared to a thinner inorganic fiber. In addition, at the time of manufacturing a pollution control apparatus, there is a tendency that scattering of the fiber pieces can be suppressed. On the other hand, there is a tendency that an inorganic fiber having a diameter of approximately 15 nm or less can suppress the generation of the fiber pieces as compared to a thicker inorganic fiber at the time of manufacturing a pollution control apparatus. The average length of the inorganic fiber may be, for example, approximately 500 to approximately 5000 nm, and may be approximately 1000 to approximately 4000 nm or approximately 1400 to approximately 3000 nm.
The diameter (average diameter) and the average length (average fiber length) of the inorganic fiber can be determined by measuring the thickness and the length of randomly extracted fibers from, for example, 50 or more micrograph images (TEM image, SEM image, and the like), and calculating the average values of the thicknesses and the lengths. The aspect ratio of the inorganic fiber is calculated by dividing an average length value by a value of the diameter.
The second inorganic fiber may have a different aspect ratio from the first inorganic fiber constituting the main body portion 1. The aspect ratio of the second inorganic fiber may be, for example, approximately 60 to approximately 2000, and may be approximately 100 to
approximately 1500, or approximately 300 to approximately 800. An inorganic fiber having an aspect ratio of approximately 60 or greater has a tendency to be capable of suppressing scattering of the fiber pieces as compared to an inorganic fiber having a smaller aspect ratio at the time of manufacturing a pollution control apparatus. On the other hand, an inorganic fiber having an
aspect ratio of approximately 2000 or less is more readily available as compared to an inorganic fiber having a larger aspect ratio. For the inorganic fiber, reference can be made to the specification of JP 2017-210815.
The inorganic adhesive is a material that expresses adhesiveness by being heated. The inorganic adhesive not only includes the inorganic adhesive that adheres due to a product formation reaction with other members, but also the inorganic adhesive that exhibits fluidity by heating, penetrates into a surface of the other member which is a contact surface, and generates adhesion by an anchoring effect (anchoring state). Although the temperature at which the adhesiveness is expressed is not limited, the adhesiveness may be expressed at a temperature of, for example, 200°C or greater, or 300°C or greater, or 600°C or greater. For example, when the holding material 10 is placed in a state interposed between two members, and after the holding material 10 is left under a temperature condition of 600°C for one hour, the holding material 10 expresses adhesiveness to other members. Adhesiveness is expressed, and thus substantial holding force of the holding material 10 can be improved effectively.
Examples of the inorganic adhesive include at least one type of salt selected from the group consisting of alkali metal salts, alkaline earth metal salts, and phosphate salts. Specific examples of the alkali metal salts include alkali metal silicates such as sodium silicate, potassium silicate, and lithium silicate. Specific examples of the alkaline earth metal salts include alkaline earth metal silicates such as magnesium silicate and calcium silicate. Specific examples of phosphate salts include aluminum phosphate, magnesium phosphate, and calcium phosphate. One type of these components may be used alone, or two or more types thereof may be used in combination.
The first material may further include an organic binder. Examples of the organic binder include an acrylic resin, a styrene-butadiene resins, an acrylonitrile resin, a polyurethane resin, natural rubber, and a polyvinyl acetate resin provided in the form of latex. Alternatively, a flexible thermoplastic resin such as an unsaturated polyester resin, an epoxy resin, and a polyvinyl ester resin may be used as the organic binder. Note that, there is a tendency that scattering of the fiber pieces can be suppressed by the first material including the organic binder.
The color of the first region Rl may be different from the color of the second region R2 in view of visibility. For example, blending ink into a liquid for forming the first region Rl enables the first region Rl to become visible. Alternatively, the first region Rl may contain a material that emits light by irradiation with black light. In this case, it is easy to confirm whether or not the first regions Rl are formed by using the black light in the inspection step after manufacturing the holding material 10.
The method of manufacturing the holding material 10 includes the steps of preparing the main body portion 1 and providing the first region Rl on at least one surface Fl of the main body
portion 1. According to the manufacturing method described above, the holding material 10 having the first region Rl formed on at least one surface Fl of the main body portion 1 can be obtained.
Note that when a mat made of inorganic fibers including an organic binder and/or inorganic fine particles is used as the main body portion 1, the following steps may be performed prior to the formation of the first regions Rl .
(a) The step of impregnating a mat made of inorganic fibers with a colloidal solution containing an organic binder and/or inorganic fine particles.
(b) The step of obtaining the main body portion 1 by drying the mat impregnated with the colloidal solution.
At step (a), in a case where the inorganic fine particles are present inside the mat, the composition of the colloidal solution is preferably adjusted such that the amount of the inorganic fine particles is approximately 1 to approximately 10 mass% based on the total mass of the main body portion 1. When the amount of the inorganic fine particles is approximately 1 mass% or greater, a sufficient surface pressure is easily obtained, and when the amount of the inorganic fine particles is approximately 10 mass% or less, sufficient flexibility is easily obtained to wind the holding material 10 around the pollution control element.
It is sufficient that the mat obtained at step (a) can be dried at step (b). For example, the mat obtained at step (a) may be dried in a hot air drier set to approximately 80 to approximately 250°C for approximately 10 to approximately 180 minutes.
The liquid used to form the first region Rl includes the first material, a component formulated as necessary (for example, ink), and water (a dispersion medium). The formation of the first region Rl may be performed, for example, by spray coating, roll coating, film transfer and curtain coating. To ensure that no liquid is applied to the second region R2, a masking tape or the like may be used to pre-mask a region corresponding to the second region R2.
The amount of application per unit area (solid mass) in the first region Rl may be, for example, approximately 1 to approximately 50 g/m2, or approximately 2 to approximately 40 g/m2, or approximately 5 to approximately 30 g/m2. Moisture may be volatilized by performing the drying step after application. For example, the main body portion 1 to which the liquid is applied to form a pattern may be dried for approximately 10 to approximately 180 minutes in a hot air drier set to approximately 80 to approximately 250°C. As a result, the first region Rl is formed on the surface of the main body portion 1.
The step of forming the first region Rl may be performed in multiple steps. Namely, a method of forming the first region Rl may include the steps of applying a liquid containing the first material to the entire surface of the main body portion 1, masking a region corresponding to the second region R2, and applying a liquid containing the first material to a region corresponding to the first region Rl in this order. Alternatively, the method of forming the first region Rl may include the steps of masking a region corresponding to the second region R2, applying a liquid
containing the first material to a region corresponding to the first region Rl, removing the mask covering the region corresponding to the second region R2, and applying a liquid containing the first material to the entire surface of the main body portion 1 in this order.
The holding material 10 is used to hold the pollution control element 30 within a pollution control apparatus 50 as illustrated in FIG. 3. Specific examples of the pollution control element 30 include a catalyst support, and a filter element for purifying exhaust gas from an engine. Specific examples of the pollution control apparatus 50 include a catalytic converter and an exhaust cleaning device (for example, a diesel particulate filter device).
The pollution control apparatus 50 illustrated in FIG. 3 includes the casing 20, the pollution control element 30 disposed within the casing 20, and the holding material 10 disposed between an inside surface of the casing 20 and an outer surface of the pollution control element 30. The pollution control apparatus 50 further includes a gas inflow port 21 configured to introduce exhaust gas into the pollution control element 30, and a gas flow outlet 22 configured to discharge exhaust gas that has passed through the pollution control element 30.
In the pollution control apparatus 50, the holding material 10 is disposed in a state interposed between the inside surface of the casing 20 and the outer surface of the pollution control element 30. In the present embodiment, the surface Fl on which the first region Rl is formed faces the inside surface of the casing 20. The width of a gap between the inside surface of the casing 20 and the outer surface of the pollution control element 30 is preferably approximately 1.5 to approximately 15 mm from the perspective of ensuring hermeticity and reducing the usage of the holding material 10. A method of compressing and assembling the holding material 10 includes a clamshell method, a stuffing method, a tourniquet method, and the like.
A catalyst to be supported on a catalyst support is typically a metal (for example, platinum, ruthenium, osmium, rhodium, iridium, nickel, palladium, and the like) and metal oxides (for example, vanadium pentoxide, titanium dioxide, and the like), and is preferably used in the form of a coating. Note that the pollution control apparatus can be constructed as a diesel particulate filter or a gasoline particulate filter by applying the filter element in place of the catalyst support.
Detailed descriptions have been given above for the preferred embodiments of the present invention. However, the present invention is not limited to the embodiments described above. For example, in the embodiment described above, there is exemplified the aspect in which the surface Fl on which the first region Rl is formed faces the inside surface of the casing 20 (see FIG. 3), but the surface Fl may face an outer circumferential surface of the pollution control element 30.
In the embodiment described above, there is exemplified the aspect in which the first region Rl is formed only on the surface Fl of the main body portion 1, but the first region Rl may be formed on both surfaces (the surface F 1 and a surface F2) of the main body portion 1.
Furthermore, in FIG. 1 and FIG. 2, there is illustrated the aspect in which the first region Rl is
formed to sink into the main body portion 1, but the first region Rl may be formed to be layered on the surface of the main body portion 1.
In the embodiment described above, the aspect in which the first region Rl has a striped pattern is exemplified, but the aspect of the first region Rl is not limited to this aspect. For example, as illustrated in FIG. 4A, the first region Rl may be formed in a lattice-like pattern. As illustrated in FIGS. 4B and 4C, the first region Rl may be formed in a dotted pattern. When the first region Rl is dot-shaped, the area proportion of the first region Rl may be, for example, 10 to 90%, and may be 15 to 80% or 20 to 70%, based on the area of the surface Fl . Note that the aspects illustrated in FIGS. 4B and 4C can also be referred to as the second region R2 being formed in a lattice pattern. The width and pitch of the stripes or lattices may be set appropriately according to the size of the holding material or flexibility required for the holding material. The holding materials 10A, 10B, 10C illustrated in FIGS. 4A to 4C include a part P in which the first region Rl and the second region R2 are interleaved with each other along the winding direction of the main body portion 1.
Further, the pattern of the first region Rl may be in an aspect as illustrated in FIGS. 5 A to 5C. In FIG. 5A, the first region Rl of a holding material 10D is formed in a wave-like pattern. The first region Rl of a holding material 10E illustrated in FIG. 5B includes a combination of a wave like pattern and a pattern of stripes extending in the winding direction. The first region Rl includes a wave shape having an amplitude in the winding direction, and thus holding force can be further improved. When the first region Rl includes a wave-like pattern, the area proportion of the first region Rl may be, for example, 10 to 90%, and may be 15 to 80% or 20 to 70%, based on the area of the surface Fl . The first region Rl of a holding material 10F is formed by a letter in FIG. 5C. The first region Rl may be formed by a marking such as a logo (not illustrated), or a combination of a letter and a marking. When the first region Rl includes a letter and/or a marking, the area proportion of the first region Rl may be, for example, 10 to 90%, and may be 15 to 80% or 20 to 70%, based on the area of the surface Fl .
EXAMPLES
The present disclosure will be described with reference to examples of the present disclosure. Note that the present invention is not limited by these examples.
Example 1
Production of main body portion
2.5 L water was placed in a stainless steel vessel of volume 10 L and stirred with a fin blade. The following raw materials were charged at 1 minute intervals to the water being stirred.
(1) Aluminum sulfate (solid content concentration 40% aqueous solution, manufactured by Nippon Light Metal Co., Ltd.): 6 g
(2) Organic binder (acrylic latex, Nipol LX874 (trade name), manufactured by Zeon Corporation): 2.6 g
(3) Colloidal silica (Snowtex O (trade name), manufactured by Nissan Chemical
Corporation): 10 g
(4) Sodium liquid aluminate (solid content 40%, Asada Chemical Industry Co., Ltd.): 3.5 g
After all the raw materials were charged, agglomerated particles were confirmed in the solution. As the next step, a needle-punched alumina fiber blanket (manufactured by Mitsubishi Chemical Corporation, MAFTEC MLS-2 blanket (trade name)) was cut into 15 cm c 40 cm. The blanket was then placed over a metal mesh, and after the solution was poured from above, the blanket was suctioned and dehydrated for 15 seconds over the metal mesh. After the blanket was impregnated with the above-described solution in this manner, the blanket was dried for 45 minutes in a hot air drier set to a temperature of l70°C. The main body portion of the holding material was produced as a result.
Formation of First Region
A liquid for forming the first region was prepared as follows. First, alumina sol AS520 (manufactured by Nissan Chemical Corporation) was prepared as a first material. A liquid was prepared by diluting the alumina sol AS520 with water such that the solid content concentration was 5%. Red ink (WMBE-5, manufactured by Orient Chemical Industries Co., Ltd.) was added to the liquid, and a coating liquid was made visible. The mixture was stirred for one minute.
A masking tape having a width of 6 mm was applied to one surface of a main body portion (a surface on the side that is in contact with an inner surface of a casing) by the width of 150 mm along a direction orthogonal to the winding direction of the main body portion. A next masking tape was applied in the same manner at the interval of 2.5 mm in the winding direction from the region where the masking tape was applied. This operation was repeated to cover a region to be the second region with the masking tape.
A spray air gun was used to spray a predetermined amount of the mixture liquid on one side of the main body portion. After the masking tape was peeled off, drying was performed for 10 minutes by a hot air dryer set to a temperature of l70°C. A holding material including a first region formed in a striped shape was obtained as a result. The area proportion of the first region was 30%, based on the overall area of one surface of the main body portion. Furthermore, the amount of the first material (alumina) per unit area of the first region was 20 g/m2.
Example 2
A holding material was prepared in the same manner as in Example 1 with the exception that a masking tape was applied as follows. That is, a masking tape having a width of 4 mm was
applied to one surface of a main body portion (a surface on the side that is in contact with an inner surface of a casing) by the width 150 mm along a direction orthogonal to the winding direction of the main body portion. A next masking tape was applied in the same manner at an interval of 4 mm in the winding direction from the region where the masking tape was applied. This operation was repeated to cover a region to be a second region with the masking tape. The area proportion of a first region was 50%, based on the overall area of one surface of the main body portion.
Example 3
A holding material was prepared in the same manner as in Example 1 with the exception that a masking tape was applied as follows. That is, a masking tape having a width of 2 mm was applied to one surface of a main body portion (a surface on the side that is in contact with an inner surface of a casing) by the width of 150 mm along a direction orthogonal to the winding direction of the main body portion. A next masking tape was applied in the same manner at an interval of 6 mm in the winding direction from the region where the masking tape was applied. This operation was repeated to cover a region to be a second region with the masking tape. The area proportion of a first region was 75%, based on the overall area of one surface of the main body portion.
Example 4
A holding material was prepared in the same manner as in Example 1 with the exception that a masking tape was applied as follows. That is, a region to be a second region was covered with a masking tape such that a first region formed a lattice-like pattern. The area proportion of the first region was 75%, based on the overall area of one surface of a main body portion.
Example 5
A holding material was prepared in the same manner as in Example 1 with the exception that a masking tape was applied as follows. That is, a region to be a second region was covered with a masking tape such that the first region formed a dotted pattern. The area proportion of a first region was 30%, based on the overall area of one surface of a main body portion.
Comparative Example 1
A main body portion prepared in the same manner as in Example 1 was used as a holding material according to Comparative Example 1. That is, in the holding material according to Comparative Example 1, a first region was not formed (the area proportion of the first region: 0%).
Comparative Example 2
A holding material was prepared in the same manner as in Example 1 with the exception that no masking tape was applied to one surface of a main body portion (a surface on the side that
is in contact with an inner surface of a casing). That is, the holding material according to
Comparative Example 2 included a first region formed across all of the one surface of the main body portion (the area proportion of the first region: 100%).
Measurement of Coefficient of Static Friction of Holding Material
A coefficient of static friction of the holding material was measured by the following procedure by using an Autograph AGS100D (registered trademark, manufactured by Shimadzu Corporation). Namely, each of the holding materials according to the examples and the comparative examples was cut into a 50 mm square to prepare a test specimen. As illustrated in FIG. 6, a test specimen 11 was secured by bonding a surface of the test specimen 11 opposite a surface 12 to be measured for the coefficient of static friction to a stainless steel plate 66 via a double -sided adhesive tape 62.
One end of a stainless steel cord 63 of approximately 1 m was secured to the stainless steel plate 66 and the other end was secured to a load cell 64 via a pulley block 65. At this time, the pulley block 65 was placed exactly beneath the load cell 64 to move the plate 66 secured to the test specimen 11 parallel to the ground when the load cell 64 was lifted.
Next, the test specimen 11 was placed on a plate 61 in a position which is parallel to the ground and at which the cord 63 is perpendicular to the central axis of the pulley block 65. A stainless steel plate was used as the plate 61 in place of the casing, and specifically, the plate was machine processed for a plate surface 2B treatment (cold rolling) to have a surface roughness Ra of 0.2 to 0.5 pm. The height of the load cell 64 was adjusted such that the test specimen 11 was at a position of the maximum distance from the pulley block 65.
A load 67 of 12 kg was placed on a plate 66. Subsequently, the load cell 64 was lifted and the cord 63 was pulled in the arrow direction at a 100 mm/minute traction. The load measured immediately before the test specimen 11 starts slipping from the surface of the plate 61 was recorded as static friction force (N). The coefficient of static friction was calculated by dividing the static friction force by the load (N) applied to the test specimen 11 including the plate 66. The results are shown in Table 1.
Evaluation of Windability
Each of the holding materials according to the examples and the comparative examples was cut into a width of 70 mm and a length of 350 mm, and was wound around an outer circumference of a catalyst support having a cylindrical shape of a length 115 mm and an outer diameter 105 mm (trade name“HONEY CERAM”, manufactured by NGK Insulators, Ltd.). A maximum gap between the pollution control element and the holding material was measured by using JIS1 grade linear scale. A holding material having a small maximum gap value can be
evaluated as being more easily wound than a holding material having a large value. The results are shown in Table 1.
Table 1
Industrial Applicability
According to the present disclosure, a holding material is provided including a surface that is easy to be wound around an outer peripheral surface of a pollution control element at the manufacturing step of a pollution control apparatus and that can improve holding force.
Furthermore, according to the present disclosure, a method of manufacturing a holding material and a pollution control apparatus including a holding material are provided.
Claims
1. A holding material wound on an outer peripheral surface of a pollution control element, the holding material comprising:
a main body portion having a sheet-like shape and including at least a first inorganic fiber; a first region provided on at least one surface of the main body portion and where a first material including at least an inorganic material is attached to the first inorganic fiber; and
a part in which, along a winding direction of the main body portion, the first region and a second region are interleaved with each other, and the first material is not attached to the second region or is attached to the second region with fewer attachment amount than to the first region.
2. The holding material according to claim 1, wherein the first region is formed to make a regular pattern on the surface.
3. The holding material according to claim 1 or 2, wherein the second region is continuously formed from one end to the other end in a width direction of the main body portion.
4. The holding material according to any one of claims 1 to 3, wherein the first region is continuously formed from one end to the other end in a width direction of the main body portion.
5. The holding material according to any one of claims 1 to 4, wherein the first region is formed to make a striped pattern.
6. The holding material according to any one of claims 1 to 3, wherein the second region is formed to make a lattice-like pattern.
7. The holding material according to any one of claims 1, 2 and 4, wherein the first region is formed to make a lattice-like pattern.
8. The holding material according to any one of claims 1 to 7, wherein the first region contains a material that emits light upon irradiation with black light.
9. The holding material according to any one of claims 1 to 8, wherein the first region is formed by a letter and/or a marking.
10. The holding material according to any one of claims 1 to 9, wherein the first region has a different color from the second region.
11. The holding material according to any one of claims 1 to 10, wherein the first material comprises a second inorganic fiber having a different aspect ratio from the first inorganic fiber.
12. The holding material according to any one of claims 1 to 11, wherein the first material comprises an inorganic particle.
13. The holding material according to any one of claims 1 to 12, wherein the first material comprises an inorganic adhesive.
14. The holding material according to any one of claims 1 to 13, wherein the first material comprises an organic binder.
15. A pollution control apparatus comprising :
a casing;
a pollution control element disposed within the casing; and
the holding material according to any one of claims 1 to 14 disposed between the casing and the pollution control element.
16. The pollution control apparatus according to claim 15, wherein the holding material at least includes the first region on a surface that is in contact with an inner surface of the casing.
17. The pollution control apparatus according to claim 15, wherein the holding material at least includes the first region on a surface that is in contact with an outer peripheral surface of the pollution control element.
18. A method of manufacturing the holding material according to any one of claims 1 to 14, the method comprising the steps of:
preparing the main body portion; and
providing the first region on at least one surface of the main body portion.
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JP2018161048A JP2020033935A (en) | 2018-08-30 | 2018-08-30 | Holding material, manufacturing method thereof and pollution control device |
JP2018-161048 | 2018-08-30 |
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US20230021664A1 (en) * | 2019-12-17 | 2023-01-26 | 3M Innovative Properties Company | Thermal insulation structure and method of making same |
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