WO1996006809A1 - Verfahren zur herstellung von faserverstärkten xerogelen, sowie ihre verwendung - Google Patents
Verfahren zur herstellung von faserverstärkten xerogelen, sowie ihre verwendung Download PDFInfo
- Publication number
- WO1996006809A1 WO1996006809A1 PCT/EP1995/003275 EP9503275W WO9606809A1 WO 1996006809 A1 WO1996006809 A1 WO 1996006809A1 EP 9503275 W EP9503275 W EP 9503275W WO 9606809 A1 WO9606809 A1 WO 9606809A1
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- WIPO (PCT)
- Prior art keywords
- gel
- fibers
- fiber
- reinforced
- sol
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract description 31
- 239000011159 matrix material Substances 0.000 claims abstract description 9
- 239000000835 fiber Substances 0.000 claims description 41
- 239000007788 liquid Substances 0.000 claims description 26
- 239000011148 porous material Substances 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 9
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 8
- -1 heteroaromatic radical Chemical class 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 7
- 238000009833 condensation Methods 0.000 claims description 6
- 230000005494 condensation Effects 0.000 claims description 6
- 239000004745 nonwoven fabric Substances 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 235000019353 potassium silicate Nutrition 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 2
- GNFTZDOKVXKIBK-UHFFFAOYSA-N 3-(2-methoxyethoxy)benzohydrazide Chemical compound COCCOC1=CC=CC(C(=O)NN)=C1 GNFTZDOKVXKIBK-UHFFFAOYSA-N 0.000 claims description 2
- 229910004013 NO 2 Inorganic materials 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 239000012774 insulation material Substances 0.000 claims description 2
- 239000003605 opacifier Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 150000003254 radicals Chemical group 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000011810 insulating material Substances 0.000 abstract 1
- 239000000499 gel Substances 0.000 description 63
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 22
- 238000001035 drying Methods 0.000 description 22
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 19
- 239000002904 solvent Substances 0.000 description 14
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 13
- 239000002657 fibrous material Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 238000013001 point bending Methods 0.000 description 9
- 239000005051 trimethylchlorosilane Substances 0.000 description 9
- 238000005259 measurement Methods 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- 239000003365 glass fiber Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003456 ion exchange resin Substances 0.000 description 6
- 229920003303 ion-exchange polymer Polymers 0.000 description 6
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 5
- 229920004935 Trevira® Polymers 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000004964 aerogel Substances 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000011490 mineral wool Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 150000004703 alkoxides Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 230000005499 meniscus Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 230000035882 stress Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- FGUUSXIOTUKUDN-IBGZPJMESA-N C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 Chemical compound C1(=CC=CC=C1)N1C2=C(NC([C@H](C1)NC=1OC(=NN=1)C1=CC=CC=C1)=O)C=CC=C2 FGUUSXIOTUKUDN-IBGZPJMESA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 2
- 230000002427 irreversible effect Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000002557 mineral fiber Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 125000000542 sulfonic acid group Chemical group 0.000 description 2
- 238000000352 supercritical drying Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- KVBYPTUGEKVEIJ-UHFFFAOYSA-N benzene-1,3-diol;formaldehyde Chemical compound O=C.OC1=CC=CC(O)=C1 KVBYPTUGEKVEIJ-UHFFFAOYSA-N 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000495 cryogel Substances 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000002276 dielectric drying Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- POPACFLNWGUDSR-UHFFFAOYSA-N methoxy(trimethyl)silane Chemical compound CO[Si](C)(C)C POPACFLNWGUDSR-UHFFFAOYSA-N 0.000 description 1
- 239000005055 methyl trichlorosilane Substances 0.000 description 1
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000013354 porous framework Substances 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011240 wet gel Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B30/00—Compositions for artificial stone, not containing binders
- C04B30/02—Compositions for artificial stone, not containing binders containing fibrous materials
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B13/00—Oxygen; Ozone; Oxides or hydroxides in general
- C01B13/14—Methods for preparing oxides or hydroxides in general
- C01B13/32—Methods for preparing oxides or hydroxides in general by oxidation or hydrolysis of elements or compounds in the liquid or solid state or in non-aqueous solution, e.g. sol-gel process
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/0091—Preparation of aerogels, e.g. xerogels
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
- C04B38/0045—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by a process involving the formation of a sol or a gel, e.g. sol-gel or precipitation processes
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/10—Solid density
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/52—Sound-insulating materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/92—Fire or heat protection feature
Definitions
- the invention relates to a process for the production of modified, fiber-reinforced xerogels with porosities greater than 60% and densities below 0.6 g / cm 3 , hereinafter referred to as "fiber-reinforced xerogels", and their use.
- Aerogels in the wider sense i.e. in the sense of "gel with air as a dispersing agent" are produced by drying a suitable gel.
- airgel in this sense includes aerogels in the narrower sense, xerogels and cryogels.
- a dried gel is referred to as an airgel in the narrower sense if the liquid of the gel is largely removed at temperatures above the critical temperature and starting from pressures above the critical pressure. If, on the other hand, the liquid of the gel is removed subcritically, for example with the formation of a liquid-vapor boundary phase, the resulting gel is referred to as a xerogel.
- the capillary pressure P c which arises during drying, is determined by the surface tension ⁇ L , the surface between the pore liquid 2 and its vapor 4 Contact angle ⁇ between the liquid meniscus and pore wall 3 and the radius r of the pore 1 (Fig. 1):
- the collapse can be avoided if the gel is dried supercritically, as described for example in EP-A-0382310, EP-A-0018955 and US-A-4,610,863, and thus the surface tension v aLJ is reduced to zero.
- the aerogels produced in this way are not very stable mechanically.
- the mechanical stability can, however, be improved by fiber reinforcement of the airgel, as described in WO93 / 06044.
- temperatures of 250 to 260 ° C and pressures between 9.7 and 15.9 MPa can be used.
- DE-A-43 42 548 and WO 94/25149 describe processes for the preparation of xerogies with densities below 0.3 g / cm 3 and porosities above 60%, which make supercritical drying of gels superfluous.
- the gels are modified by treating the inner surface, for example by silylation in the case of SiO 2 xerogels, in such a way that they can be dried in the air without collapsing.
- the xerogels produced in this way are also not very stable mechanically and break easily.
- the invention relates to a process for producing fiber-reinforced xerogels with porosities greater than 60% by volume and densities of the xerogel matrix less than 0.6 g / cm 3 , characterized in that a) a sol is produced, b) fibers are added to the sol are, c) the sol obtained in b) is converted into a gel, d) optionally the liquid contained in the gel is exchanged, e) the gel is reacted with one or more surface-modifying substances such that such a large proportion of the surface groups of the Gels is replaced by groups of the surface-modifying substance that further condensation between the surface groups on different pore surfaces is largely suppressed and / or by changing the contact angle between the pore surface and the liquid from which the capillary forces are reduced, f) if necessary, those in the gel contained liquid is exchanged and g) the result is dried at a temperature below the critical temperature of the liquid contained in the gel and a pressure of 0.001 bar up to the vapor pressure of this
- Si and Al compounds (CJ Brinker, GW Scherer, Sol-Gel Science, 1990, chapters 2 and 3) suitable for the sol-gel technique, such as Si, Al alkoxides or water glass and the like, serve as starting materials based on organic substances, such as, for example, melamine formaldehyde condensates (US Pat. No. 5,086,085) or resorcinol formaldehyde condensates (US Pat. No. 4,873,219). You can also click on Mixtures of the above materials are based.
- the sol can consist of particulate or colloidal Si or Al oxide. Si compounds, in particular water glass, are preferably used.
- the fibers added to the sol can be individual fibers, fiber mats or nonwovens. In the case of single fibers in particular, the fibers can also be added during gel formation, when the sol has already reached a high viscosity but is not yet solid.
- the sol can be converted into a gel, for example, by hydrolysis and condensation of Si or Al alkoxides, gelling of particulate or colloidal Si or Al oxide or a combination of these methods.
- the preparation of gels containing Si is described, for example, in WO93 / 06044.
- the aging of the gel generally takes place at a temperature from 20 ° C. to the boiling point of the liquid contained in the gel. If the gel liquid is, for example, water, the aging process generally takes place at 20 to 90 ° C., preferably 20 to 70 ° C., at a pH of 6 to 11, preferably 6 to 9, within 1 minute up to 48 hours, especially 15 minutes to 24 hours. If an aqueous sol was used in step a) and the pH was changed with a mineral acid, the gel should be washed with water free of electrolytes.
- the liquid contained in the gel can be replaced by the same or a different liquid in a washing process (step d). If the gel contains water, for example, it is advisable to wash the gel with a protic or aprotic organic solvent until the water content of the gel is ⁇ 5% by weight, preferably ⁇ 2% by weight.
- Steps a) to d) are generally carried out at a temperature between the freezing point of the liquid contained in the gel and 70 ° C., but at most the boiling temperature of the liquid contained in the gel.
- the surface-modifying substances used in step e) convert a large proportion of the hydrophilic or reactive surface groups on the pore surfaces to hydrophobic or surface groups unsuitable for further condensation.
- R ' is hydrogen or a non-reactive organic linear, branched, cyclic, aromatic or heteroaromatic radical such as C 1 -C 18 alkyl, preferably C 6 -C 6 alkyl, particularly preferably methyl or ethyl, cyclohexyl or phenyl; the R's are independently the same or different or can be bridged.
- the silylated gel can preferably be washed with a protic or aprotic solvent until the unreacted surface-modifying substance has essentially been removed (residual content 1 1% by weight).
- Suitable solvents are those mentioned in step d). Analogously, the solvents mentioned there as preferred are also preferred here.
- the fiber-reinforced, surface-modified gel is at temperatures from -30 to 200 ° C, preferably 0 to 100 ° C, and a pressure of 0.001 to 20 bar, preferably 0.01 to 5 bar, particularly preferably 0.1 to 2 bar, dried. Temperatures higher than 200 ° C and / or pressures higher than 20 bar are easily possible, but they are associated with unnecessary effort and bring no advantages.
- the advantage of the process according to the invention is that temperatures and pressures which are well below the critical temperatures and / or pressures for the conventional solvents are sufficient for drying. Drying is generally continued until the gel has a residual solvent content of less than 0.1% by weight.
- the drying of the gel can be significantly accelerated by using dielectric drying processes, for example microwave drying.
- the solvent in step f) is replaced by a solvent which absorbs microwaves well, such as water, ethanol or preferably acetone.
- the gels can then be quickly dried in a microwave dryer.
- the process according to the invention for producing fiber-reinforced SiO 2 xerogels with porosities greater than 60% by volume and densities of the xerogel matrix less than 0.6 g / cm 3 is preferred, characterized in that a) an aqueous water glass solution (SiO 2 concentration) ⁇ 10% by weight, preferably ⁇ 7% by weight, is adjusted to a pH value of ⁇ 3, for example with the aid of an acidic ion exchange resin or a mineral acid, and a base, generally NH 4 OH, NaOH, to the resulting silica.
- Inorganic fibers such as glass fibers or mineral fibers, organic fibers such as polyester fibers, aramid fibers, nylon fibers or fibers of plant origin, and mixtures thereof can be used as the fiber material.
- the fibers can also be coated, for example polyester fibers, which are metallized with a metal such as aluminum. For better dispersibility of the fibers or wetting of the nonwoven, the fibers can be coated with a suitable size. The coating can also serve to better bind the gel to the fibers.
- the volume fraction of the fibers should be 0.1 to 30%, preferably 0.1 to 10% and b) the thermal conductivity of the fiber material should be as low as possible, preferably ⁇ 1 W / mK.
- the fiber diameter in a) non-metallized fibers should preferably be 0.1 to 30 ⁇ m and / or in b) metallized fibers preferably 0.1 to 20 ⁇ m.
- the fibers can e.g. can be introduced as disordered or aligned fibers.
- Nonwovens or mats can also be used, it also being possible to stack several nonwovens or mats on top of one another. In the case of layering mats with a preferred direction, changing the preferred direction from one layer to the next is advantageous.
- the use of nonwovens or mats has the advantage that cracks can occur in the xerogel matrix when the bending stress is high, but the xerogel matrix does not break through the nonwoven.
- Fiber-reinforced gel plates with a thickness between 0.5 and 5 mm are particularly advantageous for solvent exchange and drying, since the duration for the exchange of solvents or the drying time is essentially determined by the diffusion of the solvent or the solvent vapor.
- the fiber-reinforced xerogels thus obtained are hydrophobic if the surface groups applied by the surface modification are hydrophobic, e.g. when using trimethylchlorosilane.
- the hydrophobicity can subsequently be reduced, for example, by heating or partial pyrolysis.
- Thicker plates made of fiber-reinforced Xerogeien can be z. B. by placing in a suitable envelope, by gluing or by a suitable mechanical connection such as staples or sewing.
- the surface of the fiber-reinforced xerogel can be discussed with the person skilled in the art known materials such as plastic films, paper, cardboard, nonwovens or fabrics, are laminated.
- the fiber-reinforced xerogels obtained by the process according to the invention are suitable as heat insulation materials.
- suitable translucent fibers e.g. Glass fibers
- the bending stiffness of the panels can be varied by the choice of the fiber material used.
- decorative effects can be achieved in addition to the insulating effect.
- Figure 1 shows a schematic representation of a pore 1, which is approximately half-filled with pore liquid 2 and steam 4, the contact angle ⁇ occurring between the liquid meniscus and pore wall 3 and the radius r of the pore.
- TEOS tetraethyl orthosilicate
- the aged gel cooled to room temperature, was placed in ethanol and then heated at 50 ° C for 1 hour. This process was repeated twice with fresh ethanol and then once with n-hexane. The n-hexane was then exchanged three more times, and the sample was stored at 50 ° C. for a further 24 hours.
- TMCS trimethylchlorosilane
- the drying was then carried out in three stages over 24 hours at 37 ° C, 50 ° C and 140 ° C.
- Table 1 shows the results of the tests.
- the thermal conductivity was determined using a heating wire method (O. Nielsson, G. Joschenpöhler, J. classical, J. Fricke, High Temperatures-High Pressures, 21 (1989), 267-274), the module and the breaking stress using a three-point Bending method (e.g. GW Scherer, SA Pardenek, RM Swiatek, J. Non-Crystalline Solids, 107 (1988), 14-22).
- the fiber-reinforced Xerogel did not break in the three-point bending measurement at a certain tension, but only deformed irreversibly under high loads.
- HMA Hoechst aramid
- the fiber-reinforced Xerogel did not break at a certain tension in the three-point bending measurement, but only deformed under high loads irreversible.
- Example 2 The tests were carried out as in Example 1, with the fiber material being a
- the fiber-reinforced Xerogel did not break in the three-point bending measurement at a certain tension, but only deformed irreversibly under high loads.
- Example 2 The tests were carried out as in Example 1, with the fiber material being a
- Polyester fleece TREVIRA SPUNBOND ® with a basis weight of 70 kg / m 3 was used. The results are summarized in Table 1.
- the fiber-reinforced Xerogel did not break in the three-point bending measurement at a certain tension, but only deformed irreversibly under high loads.
- the fiber-reinforced Xerogel did not break in the three-point bending measurement at a certain tension, but only deformed irreversibly under high loads.
- a polyester fleece each made of 50% TREVIRA 290 with 0.9 dtex and 1.7 dtex with a density of 15 kg / m 3 , needled with 150 stitches / cm 2 , was then introduced into the gellable solution.
- the proportion of the fleece is 5% by volume in relation to the gel.
- the resulting gel was then left to age at 50 ° C. for a further 24 hours.
- the water contained in the gel was first extracted with 3 l of ethanol.
- the ethanol was then replaced with 3 l of n-heptane.
- the hexane-containing gel was silylated with trimethylchlorosilane (TMCS) (0.05 g TMCS per gram of wet gel), then washed again with 0.5 l of n-hexane.
- TMCS trimethylchlorosilane
- the fiber-reinforced Xerogel did not break in the three-point bending measurement at a certain tension, but only deformed irreversibly under high loads.
- the modulus of elasticity was 2 MPa.
- Example 6 the experiment was carried out with glass fibers.
- the fiber-reinforced Xerogel did not break in the three-point bending measurement at a certain tension, but only deformed irreversibly under high loads.
- the elastic modulus was 10 MPa.
- Table 2 Experimental results for drying TEOS xerogels with microwaves from ethanol at 50 W power
- a gel was prepared as in Example 3. Before drying, a solvent exchange with ethanol was carried out. Drying was carried out with a nitrogen stream heated to 80 ° C. for a drying time of 60
- Xerogel plates were produced on the basis of water glass according to the following procedure: a glass fiber fleece with a weight per unit area of 300 g / m 2 and one
- Thickness of 3 mm PolyMat glass needle mat type G300 from Schuller,
- Wertheim was annealed at 500 ° C for 1 hour.
- the fleece was placed in a mold and the sol was poured over it so that the
- the plate was then washed with acetone until the water content was below 0.5
- TMCS trimethylchlorosilane
- Drying was carried out in two stages, 24 hours at 50 ° C and 850 mbar
- the density of the composite material was 0.25 g / cm 3 .
- the thermal conductivity was determined as in Example 1. A value of 17 mW / mK was found for the thermal conductivity.
- the xerogel plate did not break during the three-point bending measurement at a certain stress, but only irreversibly deformed under high loads.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Dispersion Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Silicon Compounds (AREA)
- Reinforced Plastic Materials (AREA)
- Glass Compositions (AREA)
- Thermal Insulation (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Toys (AREA)
- Inorganic Fibers (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
Abstract
Description
Claims
Priority Applications (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MX9701587A MX9701587A (es) | 1994-08-29 | 1995-08-17 | Procedimiento para producir xerogeles reforzado con fibra y su uso. |
DE59504435T DE59504435D1 (de) | 1994-08-29 | 1995-08-17 | Verfahren zur herstellung von faserverstärkten xerogelen, sowie ihre verwendung |
RU97104883A RU2146661C1 (ru) | 1994-08-29 | 1995-08-17 | Способ получения упрочненных волокнами ксерогелей и их применение |
BR9508644A BR9508644A (pt) | 1994-08-29 | 1995-08-17 | Processo para preparação de xerogéis reforçados por fibra assim como sua aplicação |
EP95929888A EP0778815B1 (de) | 1994-08-29 | 1995-08-17 | Verfahren zur herstellung von faserverstärkten xerogelen, sowie ihre verwendung |
JP50845596A JP3897125B2 (ja) | 1994-08-29 | 1995-08-17 | 繊維−強化キセロゲルを製造する方法およびそれらの使用 |
DK95929888T DK0778815T3 (da) | 1994-08-29 | 1995-08-17 | Fremgangsmåde til fremstilling af fiberforstærkede xerogeler samt deres anvendelse |
PL95318900A PL180069B1 (pl) | 1994-08-29 | 1995-08-17 | Sposób wytwarzania kserozeli wzmocnionych wlóknem PL PL PL PL PL PL PL |
AU33467/95A AU694797B2 (en) | 1994-08-29 | 1995-08-17 | Process for producing fibre-reinforced xerogels and their use |
US08/793,543 US5866027A (en) | 1994-08-29 | 1995-08-17 | Process for producing fiber-reinforced xerogels and their use |
NO19970867A NO312828B1 (no) | 1994-08-29 | 1997-02-26 | Fremgangsmåte for fremstilling av fiberforsterkende xerogeler samt anvendelse derav |
FI970809A FI970809A (fi) | 1994-08-29 | 1997-02-26 | Menetelmä kuituvahvistettujen kserogeelien valmistamiseksi sekä niiden käyttö |
GR990400583T GR3029487T3 (en) | 1994-08-29 | 1999-02-25 | Process for producing fibre-reinforced xerogels and their use |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4430669A DE4430669A1 (de) | 1994-08-29 | 1994-08-29 | Verfahren zur Herstellung von faserverstärkten Xerogelen, sowie ihre Verwendung |
DEP4430669.5 | 1994-08-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996006809A1 true WO1996006809A1 (de) | 1996-03-07 |
Family
ID=6526851
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1995/003275 WO1996006809A1 (de) | 1994-08-29 | 1995-08-17 | Verfahren zur herstellung von faserverstärkten xerogelen, sowie ihre verwendung |
Country Status (19)
Country | Link |
---|---|
US (1) | US5866027A (de) |
EP (1) | EP0778815B1 (de) |
JP (1) | JP3897125B2 (de) |
KR (1) | KR100366475B1 (de) |
CN (1) | CN1044597C (de) |
AT (1) | ATE174017T1 (de) |
AU (1) | AU694797B2 (de) |
BR (1) | BR9508644A (de) |
CA (1) | CA2198732A1 (de) |
DE (2) | DE4430669A1 (de) |
DK (1) | DK0778815T3 (de) |
ES (1) | ES2126926T3 (de) |
FI (1) | FI970809A (de) |
GR (1) | GR3029487T3 (de) |
MX (1) | MX9701587A (de) |
NO (1) | NO312828B1 (de) |
PL (1) | PL180069B1 (de) |
RU (1) | RU2146661C1 (de) |
WO (1) | WO1996006809A1 (de) |
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US6481649B1 (en) | 1997-05-02 | 2002-11-19 | Cabot Corporation | Method for granulating aerogels |
US6620355B1 (en) | 1997-05-02 | 2003-09-16 | Cabot Corporation | Method for compacting aerogels |
US7297718B2 (en) | 1998-01-14 | 2007-11-20 | Cabot Corporation | Method of producing substantially spherical lyogels in water insoluble silylating agents |
JP2011080064A (ja) * | 1997-01-24 | 2011-04-21 | Cabot Corp | 物体音および/または衝撃音減衰のためのエアロゲルの使用法 |
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1994
- 1994-08-29 DE DE4430669A patent/DE4430669A1/de not_active Withdrawn
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1995
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- 1995-08-17 DK DK95929888T patent/DK0778815T3/da active
- 1995-08-17 AU AU33467/95A patent/AU694797B2/en not_active Ceased
- 1995-08-17 ES ES95929888T patent/ES2126926T3/es not_active Expired - Lifetime
- 1995-08-17 AT AT95929888T patent/ATE174017T1/de not_active IP Right Cessation
- 1995-08-17 US US08/793,543 patent/US5866027A/en not_active Expired - Lifetime
- 1995-08-17 CN CN95195325A patent/CN1044597C/zh not_active Expired - Lifetime
- 1995-08-17 PL PL95318900A patent/PL180069B1/pl not_active IP Right Cessation
- 1995-08-17 JP JP50845596A patent/JP3897125B2/ja not_active Expired - Lifetime
- 1995-08-17 RU RU97104883A patent/RU2146661C1/ru active
- 1995-08-17 KR KR1019970701252A patent/KR100366475B1/ko not_active IP Right Cessation
- 1995-08-17 DE DE59504435T patent/DE59504435D1/de not_active Expired - Lifetime
- 1995-08-17 CA CA002198732A patent/CA2198732A1/en not_active Abandoned
- 1995-08-17 BR BR9508644A patent/BR9508644A/pt not_active IP Right Cessation
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1997
- 1997-02-26 NO NO19970867A patent/NO312828B1/no not_active IP Right Cessation
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1999
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6210751B1 (en) * | 1995-11-09 | 2001-04-03 | Cabot Corporation | Process for preparing organically modified aerogels in which the salts formed are precipitated out |
US5877100A (en) * | 1996-09-27 | 1999-03-02 | Cabot Corporation | Compositions and insulation bodies having low thermal conductivity |
JP2011080064A (ja) * | 1997-01-24 | 2011-04-21 | Cabot Corp | 物体音および/または衝撃音減衰のためのエアロゲルの使用法 |
US6481649B1 (en) | 1997-05-02 | 2002-11-19 | Cabot Corporation | Method for granulating aerogels |
US6620355B1 (en) | 1997-05-02 | 2003-09-16 | Cabot Corporation | Method for compacting aerogels |
US6378229B1 (en) | 1997-12-19 | 2002-04-30 | Cabot Corporation | Method for the sub-critical drying of lyogels to produce aerogels |
US7297718B2 (en) | 1998-01-14 | 2007-11-20 | Cabot Corporation | Method of producing substantially spherical lyogels in water insoluble silylating agents |
Also Published As
Publication number | Publication date |
---|---|
RU2146661C1 (ru) | 2000-03-20 |
JP3897125B2 (ja) | 2007-03-22 |
EP0778815B1 (de) | 1998-12-02 |
BR9508644A (pt) | 1997-11-25 |
US5866027A (en) | 1999-02-02 |
GR3029487T3 (en) | 1999-05-28 |
CN1158598A (zh) | 1997-09-03 |
AU3346795A (en) | 1996-03-22 |
DE4430669A1 (de) | 1996-03-07 |
MX9701587A (es) | 1997-05-31 |
PL318900A1 (en) | 1997-07-21 |
NO312828B1 (no) | 2002-07-08 |
FI970809A0 (fi) | 1997-02-26 |
DE59504435D1 (de) | 1999-01-14 |
PL180069B1 (pl) | 2000-12-29 |
JPH10504793A (ja) | 1998-05-12 |
AU694797B2 (en) | 1998-07-30 |
ES2126926T3 (es) | 1999-04-01 |
ATE174017T1 (de) | 1998-12-15 |
CN1044597C (zh) | 1999-08-11 |
FI970809A (fi) | 1997-02-26 |
KR970705525A (ko) | 1997-10-09 |
EP0778815A1 (de) | 1997-06-18 |
NO970867D0 (no) | 1997-02-26 |
KR100366475B1 (ko) | 2003-04-26 |
CA2198732A1 (en) | 1996-03-07 |
NO970867L (no) | 1997-02-26 |
DK0778815T3 (da) | 1999-08-16 |
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