Facade System and Insulation Element for a Facade System
20240318421 ยท 2024-09-26
Assignee
Inventors
Cpc classification
B01J20/28004
PERFORMING OPERATIONS; TRANSPORTING
C04B2201/30
CHEMISTRY; METALLURGY
B01J20/3042
PERFORMING OPERATIONS; TRANSPORTING
B32B2262/16
PERFORMING OPERATIONS; TRANSPORTING
B32B5/26
PERFORMING OPERATIONS; TRANSPORTING
C04B2103/30
CHEMISTRY; METALLURGY
B01J20/24
PERFORMING OPERATIONS; TRANSPORTING
E04D11/02
FIXED CONSTRUCTIONS
Y02B80/32
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
D04H1/60
TEXTILES; PAPER
B32B3/18
PERFORMING OPERATIONS; TRANSPORTING
E04B2001/742
FIXED CONSTRUCTIONS
B01J20/2803
PERFORMING OPERATIONS; TRANSPORTING
Y02A30/254
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
C08L2205/06
CHEMISTRY; METALLURGY
B32B5/02
PERFORMING OPERATIONS; TRANSPORTING
C08K2201/014
CHEMISTRY; METALLURGY
C04B24/32
CHEMISTRY; METALLURGY
E04D11/002
FIXED CONSTRUCTIONS
International classification
Abstract
The invention relates to a fa?ade system for a building, in particular an External Thermal Insulation Composite System (ETICS), comprising a thermal and/or acoustic insulation, consisting of at least one insulation element being a bonded mineral fibre product made of mineral fibres, preferably stone wool fibres, and a cured aqueous binder composition free of phenol and formaldehyde, wherein the insulation element is fixed to an outer surface of the building by mechanical fastening elements and/or an adhesive, covered with a rendering, and whereby the aqueous binder composition prior to curing comprises a component (i) in form of one or more lignosulfonate lignins having a carboxylic acid group content of 0.03 to 2.0 mmol/g, based on the dry weight of the lignosulfonate lignins and a component (ii) in form of one or more cross-linkers, and wherein the insulation element has a bulk density between 70 kg/m.sup.3 and 150 kg/m.sup.3.
Claims
1. A fa?ade system for a building, in particular an External Thermal Insulation Composite System (ETICS), comprising a thermal and/or acoustic insulation, consisting of at least one insulation element being a bonded mineral fibre product made of mineral fibres, preferably stone wool fibres, and a cured aqueous binder composition free of phenol and formaldehyde, wherein the insulation element is fixed to an outer surface of the building by mechanical fastening elements and/or an adhesive, covered with a rendering, and whereby the aqueous binder composition prior to curing comprises a component (i) in form of one or more lignosulfonate lignins having a carboxylic acid group content of 0.03 to 2.0 mmol/g, based on the dry weight of the lignosulfonate lignins and a component (ii) in form of one or more cross-linkers, and wherein the insulation element has a bulk density between 70 kg/m.sup.3 and 150 kg/m.sup.3.
2. A fa?ade system according to claim 1, wherein the aqueous binder composition additionally comprises a component (iii) in form of one or more plasticizers.
3. A fa?ade system according to claim 1, wherein the insulation element has a loss on ignition (LOI) within the range of 2 to 8 wt.-%, preferably 2 to 5 wt.-%.
4. A fa?ade system according to any of the preceding claims, having insulation elements with a compression strength between 5 and 90 kPa measured in accordance with European Standard EN 826:2013.
5. A fa?ade system according to any of the preceding claims, having insulation elements with a delamination strength between 5 and 100 kPa measured in accordance with European Standard EN 1607:2013
6. A fa?ade system according to any of the preceding claims, wherein component (i) is having a carboxylic acid group content of 0.05 to 0.6 mmol/g, based on the dry weight of lignosulfonate lignins.
7. A fa?ade system according to any of the preceding claims, wherein component (i) is in form of one or more lignosulfonate lignins having an average carboxylic acid group content of less than 1.8 groups per macromolecule considering the M_n wt. average of component (i), such as less than 1.4 such as less than 1.1 such as less than 0.7 such as less than 0.4.
8. A fa?ade system according to any of the preceding claims, wherein component (i) is having a content of phenolic OH groups of 0.3 to 2.5 mmol/g, such as 0.5 to 2.0 mmol/g, such as 0.5 to 1.5 mmol/g, based on the dry weight of lignosulfonate lignins.
9. A fa?ade system according to any of the preceding claims, wherein component (i) is having a content of aliphatic OH groups of 1.0 to 8.0 mmol/g, such as 1.5 to 6.0 mmol/g, such as 2.0 to 5.0 mmol/g, based on the dry weight of lignosulfonate lignins.
10. A fa?ade system according to any of the preceding claims, wherein the component (i) comprises ammoniumlignosulfonates and/or calciumlignosulfonates, and/or magnesiumlignosulfonates, and any combinations thereof.
11. A fa?ade system according to any of the preceding claims, wherein component (i) comprises ammoniumlignosulfonates and calciumlignosulfonates, wherein the molar ratio of NH.sub.4.sup.+ to Ca.sup.2+ is in the range of 5:1 to 1:5, in particular 3:1 to 1:3.
12. A fa?ade system according to any of the preceding claims, wherein the aqueous binder composition contains added sugar in an amount of 0 to less than 5 wt.-%, based on the weight of lignosulfonate and sugar.
13. A fa?ade system according to any of the preceding claims, wherein the aqueous binder composition comprises component (i) in an amount of 50 to 98 wt.-%, such as 65 to 98 wt.-%, such as 80 to 98 wt.-%, based on the dry weight of components (i) and (ii).
14. A fa?ade system according to any of the preceding claims, wherein the component (ii) is in form of one or more cross-linkers selected from ?-hydroxyalkylamide-cross-linkers, and/or oxazoline-cross-linkers, and/or the group consisting of multifunctional organic amines such as an alkanolamine, diamines, such as hexamethyldiamine, and/or epoxy compounds having a molecular weight of more than 500, such as an epoxidised oil based on fatty acid triglyceride or one or more flexible oligomer or polymer, such as a low Tg acrylic based polymer, such as a low Tg vinyl based polymer, such as low Tg polyether, which contains reactive functional groups such as carbodiimide groups, such as anhydride groups, such as oxazoline groups, such as amino groups, such as epoxy groups, and/or one or more cross-linkers selected from the group consisting of fatty amines; and/or one more cross-linkers in form of fatty amides; and/or one or more cross-linkers selected from polyester polyols, such as polycaprolactone; and/or one or more cross-linkers selected from the group consisting of starch, modified starch, CMC; and/or one or more cross-linkers in form of multifunctional carbodiimides, such as aliphatic multifunctional carbodiimides; and/or one or more cross-linkers selected from melamine based cross-linkers, such as a hexakis(methylmethoxy)melamine (HMMM) based cross-linkers.
15. A fa?ade system according to any of the preceding claims, wherein the component (ii) comprises one or more cross-linkers selected from ?-hydroxyalkylamide-cross-linkers and/or oxazoline-cross-linkers.
16. A fa?ade system according to any of the preceding claims, comprising component (ii) in an amount of 1 to 50 wt.-%, such as 4 to 20 wt.-%, such as 6 to 12 wt.-%, based on the dry weight of component (i).
17. A fa?ade system according to any of the preceding claims, wherein the component (ii) is in form of one or more cross-linkers selected from ?-hydroxyalkylamide-cross-linkers, such as N-(2-hydroxyisopropyl)amide-cross-linkers, such as N-(2-hydroxyethyl)amide-cross-linkers, such as N-(2-hydroxyethyl)adipamide-cross-linkers, such as N,N,N,N-tetrakis(2-hydroxyethyl)adipamide and/or the group consisting of multifunctional organic amines such as an alkanolamine, diamines, such as hexamethyldiamine, and/or epoxy compounds having a molecular weight of more than 500, such as an epoxidised oil based on fatty acid triglyceride or one or more flexible oligomer or polymer, such as a low Tg acrylic based polymer, such as a low Tg vinyl based polymer, such as low Tg polyether, which contains reactive functional groups such as carbodiimide groups, such as anhydride groups, such as oxazoline groups, such as amino groups, such as epoxy groups, and/or one or more cross-linkers in form of multifunctional carbodiimides, such as aliphatic multifunctional carbodiimides.
18. A fa?ade system according to any of the preceding claims, wherein the component (ii) comprises one or more cross-linkers selected from ?-hydroxyalkylamide-cross-linkers, such as N-(2-hydroxyisopropyl)amide-cross-linkers, such as N-(2-hydroxyethyl)amide-cross-linkers, such as N-(2-hydroxyethyl) adipamide-cross-linkers, such as N,N,N,N-tetrakis(2-hydroxyethyl)adipamide.
19. A fa?ade system according to any of the preceding claims, comprising component (ii) in an amount of 2 to 90 wt.-%, such as 6 to 60 wt.-%, such as 10 to 40 wt.-%, such as 25 to 40 wt.-%, based on the dry weight of component (i).
20. A fa?ade system according to any of the preceding claims, wherein component (iii) is in form of one or more plasticizers selected from the group consisting of fatty alcohols, monohydroxy alcohols, such as pentanol, stearyl alcohol; and/or one or more plasticizers selected from the group consisting of alkoxylates such as ethoxylates, such as butanol ethoxylates, such as butoxytriglycol; and/or one or more plasticizers in form of propylene glycols; and/or one or more plasticizers in form of glycol esters; and/or one or more plasticizers selected from the group consisting of adipates, acetates, benzoates, cyclobenzoates, citrates, stearates, sorbates, sebacates, azelates, butyrates, valerates; and/or one or more plasticizers selected from the group consisting of phenol derivatives, such as alkyl or aryl substituted phenols; and/or one or more plasticizers selected from the group consisting of silanols, siloxanes; and/or one or more plasticizers selected from the group consisting of sulfates such as alkyl sulfates, sulfonates such as alkyl aryl sulfonates such as alkyl sulfonates, phosphates such as tripolyphosphates; and/or one or more plasticizers in form of hydroxy acids; and/or one or more plasticizers selected from the group consisting of monomeric amides, such as acetamides, benzamide, fatty acid amides such as tall oil amides; and/or one or more plasticizers selected from the group consisting of quaternary ammonium such compounds as trimethylglycine, distearyldimethylammoniumchloride; and/or one or more plasticizers selected from the group consisting of vegetable oils such as castor oil, palm oil, linseed oil, soybean oil; and/or tall oil, and/or one or more plasticizers selected from the group consisting of hydrogenated oils, acetylated oils; and/or one or more plasticizers selected from acid methyl esters; and/or one or more plasticizers selected from the group consisting of alkyl polyglucosides, gluconamides, aminoglucoseamides, sucrose esters, sorbitan esters; and/or one or more plasticizers selected from the group consisting of polyethylene glycols, polyethylene glycol ethers; and/or one or more plasticizers in form of polyols, such as glycerol, such as 1,1,1-Tris(hydroxymethyl)propane; and/or triethanolamine.
21. A fa?ade system according to any of the preceding claims, wherein component (iii) is in form of propylene glycols, phenol derivatives, silanols, siloxanes, hydroxy acids, vegetable oils, polyethylene glycols, polyethylene glycol ethers, triethanolamine, or any mixtures thereof.
22. A fa?ade system according to any of the preceding claims, wherein component (iii) comprises one or more plasticizers having a boiling point of 100 to 380? C., more preferred 120 to 300? C., more preferred 140 to 250? C.
23. A fa?ade system according to any of the preceding claims, wherein component (iii) comprises one or more polyethylene glycols having an average molecular weight of 150 to 50000 g/mol, in particular 150 to 4000 g/mol, more particular 150 to 1000 g/mol, preferably 150 to 500 g/mol, more preferably 200 to 400 g/mol.
24. A fa?ade system according to any of the preceding claims, wherein the component (iii) is present in an amount of 0.5 to 60, preferably 2.5 to 25, more preferably 3 to 15 wt.-%, based on the dry weight of component (i).
25. A fa?ade system according to any of the preceding claims, wherein the binder composition prior to curing comprises a further component (iv) in form of one or more coupling agents, such as organofunctional silanes.
26. A fa?ade system according to any of the preceding claims, wherein in the binder composition prior to curing further comprises a component (v) in form of one or more components selected from the group of bases, such as ammonia, such as alkali metal hydroxides, such as KOH, such as earth alkaline metal hydroxides, such as Ca(OH).sub.2, such as Mg(OH).sub.2, such as amines or any salts thereof.
27. A fa?ade system according to any of the preceding claims, wherein the binder composition prior to curing comprises a further component in form of urea, in particular in an amount 5 to 40 wt.-%, such as 10 to 30 wt.-%, such as 15 to 25 wt.-%, based on the dry weight of component (i).
28. A fa?ade system according to any of the preceding claims, wherein the binder composition prior to curing comprises a further component (vi) in the form of one or more reactive or nonreactive silicones.
29. A fa?ade system according to any of the preceding claims, wherein the insulation element does not contain an ammonia-oxidized lignin (AOL).
30. An insulation element for a fa?ade system according to any of the preceding claims 1 to 29, made of mineral fibres, preferably stone wool fibres, and a cured aqueous binder composition free of phenol and formaldehyde, wherein the aqueous binder composition prior to curing comprises a component (i) in form of one or more lignosulfonate lignins having a carboxylic acid group content of 0.03 to 2.0 mmol/g, based on the dry weight of the lignosulfonate lignins, a component (ii) in form of one or more cross-linkers and wherein the insulation element has a bulk density between 70 kg/m.sup.3 and 150 kg/m.sup.3.
31. An insulation element according to claim 30, wherein the aqueous binder composition additionally comprises a component (iii) in form of one or more plasticizers.
32. An insulation element according to claim 30 or 32, further comprising the features of the insulation element of any of claims 2 to 29.
Description
[0456] The invention is illustrated in the accompanying drawings in which
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[0469] A first embodiment of a fa?ade system is shown in
[0470] The insulation shown in
[0471] Instead of a one layered insulation plate 2 multilayered insulation plates can be used, each having at least two layers of different density. These insulation plates are so-called dual-density plates and are shown in a second embodiment according to
[0472] The insulation plate 2 may also be a mineral wool lamella plate which consists of several lamellas of mineral wool glued together in their length direction to form the plate and where the mineral fibre direction is predominantly perpendicular to the major surface as is conventional for such mineral wool lamella plates. The thickness is 100 mm and the width by length is 400 by 1200 mm and the density of the mineral wool plate is 75 kg/m.sup.3.
[0473] A plate 3 (
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[0476] The insulation shown in
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[0478]
[0479] The head 8 exerts a pressure on the surface of the insulation plate 2 and there is an indentation 9 into the surface due to the static hold force of the mounted screw and the mineral wool of insulation plate 2 is compressed between the fastener head 8 and the surface of the plate 3.
[0480] The total system of fasteners 4, the sandwich of the aerogel and mineral fibres containing plate 3 and the two outside layered insulation plates 2 is mechanically rigid and has improved properties over a sub-system exclusively consisting of mineral wool plates; the pull-through resistance is in particular improved but also the overall weight is lowered.
[0481] The insulation shown in
[0482]
[0483] The head 8 exerts a pressure on the surface of the composite plate 12 and there is an indentation 9 into the surface due to the static hold force of the mounted screw 6 and the composite plate 12 is compressed between the fastener head 8 and the surface of the composite plate 12.
[0484] The total system of fasteners 4, mineral wool-aerogel-composite plate 12 is mechanically rigid and has improved properties over a sub-system exclusively consisting of mineral wool; the pull-through resistance is in particular improved but also the overall weight is lowered.
[0485] The insulation shown in
[0486] According to the invention, the binder used in the insulation element 2, 3, 12 and/or for the connection of the insulation elements 2, 3, 12 to each other comprises a first component in form of one or more lignosulfonate lignins, e.g. following Example 54 as described above.
[0487] The diagram according to
[0488] The delamination strength is measured according to EN 1607:2013 and the first initial measurement is carried out on unaged samples immediately or shortly after production of the insulation element. This initial testing and the respective average result of a representative number of samples is illustrated at time 0 on the x-axis of the diagram. Said time 0 corresponds with day 0 respectively the start of the accelerated ageing test according to the following description below.
[0489] In order to determine the ageing resistance of mineral fibre products exposed to moisture and heating during the service life of constructions, such mineral fibre products with focus on mechanical properties are subjected to accelerated ageing. The ageing resistance is defined as the ability of the product to maintain the original mechanical properties, and it is calculated as the aged strength in percent of the original strength. The test procedure follows the so called Nordtest method NT Build 434:1995.05, extended to 28 days. The aim of said method is to expose insulation materials to accelerated ageing due to increased temperature and heat. It is applicable to all insulation materials manufactured as insulation boards. The method is not predictive i.e. it is not intended for assessment of the service life, but it is a precondition for a satisfactory performance that ageing due to this method does not cause major changes in the properties of the materials under investigation. Experiences over more than two decades with the Nordtest method have proven to deliver reliable data to ensure satisfactory mechanical performance of inter alia mineral fibre products as insulation elements for use in fa?ade systems.
[0490] According to the method, a representative number of test specimens are exposed to heat-moisture action for 7, 14 and 28 days at 70?2? C. and 95?5% relative humidity (RH) in a climatic chamber. Subsequently, the specimens are placed at 23?2? C. and 50?5% RH for at least 24 hours and upon drying are prepared for testing of mechanical performance, like e.g. the delamination strength is measured according to EN 1607:2013, or compression strength according to EN 826:2013 as will be described further below.
[0491] The relative ageing resistance is then calculated in % of and based on the initial absolute value measured at time 0.
[0492] Results are documented and illustrated for 7, 14 and 28 days of accelerated ageing.
[0493] With respect to the
[0494] The following Table I shows the delamination strength [kPa] EN 1607 according to
TABLE-US-00008 TABLE I 0 days 7 days 14 days 28 days A.sub.2 25.5 17.1 16.5 15.8 B.sub.2 27.1 14.7 14.9 12.4 C.sub.2 16.8 11.9 11.2 9.7
[0495] Table I shows the absolute delamination strength of the insulation element according to the invention (C.sub.2) compared to an insulation element containing a phenol-formaldehyde binder (A.sub.2) and to an insulation element containing a non-added formaldehyde binder (B.sub.2) initially and after accelerated ageing. The corresponding graphs are shown in
[0496] The following Table II shows the relative delamination strength according to table I in % of initial according to
TABLE-US-00009 TABLE II 0 days 7 days 14 days 28 days A.sub.3 100.0 67.1 64.7 62.0 B.sub.3 100.0 54.2 55.0 45.8 C.sub.3 100.0 70.8 66.7 57.7
[0497] Table II shows the relative delamination strength of the insulation element according to the invention (C.sub.3) compared to an insulation element containing a phenol-formaldehyde binder (A.sub.3) and to an insulation element containing a non-added formaldehyde binder (B.sub.3). The corresponding graphs are shown in
[0498] In Table I and especially in Table II it can be seen that the delamination strength of the insulation element 4 according to the invention (C.sub.2; C.sub.3) does not differ that much from the delamination strength of the insulation element (A.sub.2; A.sub.3) containing a phenol-formaldehyde binder. Furthermore, it can be seen that the loss of delamination strength of the insulation element containing a non-added formaldehyde binder (B.sub.2; B.sub.3) increases much more than the delamination strength of the insulation element 4 according to the invention (C.sub.2; C.sub.3).
[0499] From Table II and
[0500] In particular, it can be seen from Table II and from
[0501] The following Table III shows the absolute compression strength [kPa] EN 826 according to
TABLE-US-00010 TABLE III 0 days 7 days 14 days 28 days A.sub.4 76.8 60.5 61.6 56.5 B.sub.4 80.6 64.0 55.6 52.6 C.sub.4 67.4 53.1 49.9 49.5
[0502] Table III shows the absolute compression strength of the insulation element according to the invention (C.sub.4) compared to an insulation element containing a phenol-formaldehyde binder (A.sub.4) and to an insulation element containing a non-added formaldehyde binder (B.sub.4). The corresponding graphs are shown in
[0503]
[0504] The compression strength is measured according to EN 826 and it can be seen, that the compression strength is measured immediately after production of the insulation element 4, and seven, fourteen and twenty-eight days after production of the insulation element 4 including accelerated ageing.
[0505] The following Table IV shows the relative compression strength according to table III in % of initial according to
TABLE-US-00011 TABLE IV 0 days 7 days 14 days 28 days A.sub.5 100.0 78.8 80.2 73.6 B.sub.5 100.0 79.4 69.0 65.3 C.sub.5 100.0 78.8 74.0 73.4
[0506] Table IV shows the relative compression strength of the insulation element according to the invention (C.sub.5) compared to an insulation element containing a phenol-formaldehyde binder (A.sub.5) and to an insulation element containing a non-added formaldehyde binder (B.sub.5). The corresponding graphs are shown in
[0507] From
[0508] Furthermore, it can be seen from
[0509] Hence, measurements have proven the binder and respective insulation elements produced with the binder according to the invention to provide a high ageing resistance comparably good as for state of the art phenol-formaldehyde binder.