CA2056918A1 - Composite foams of low thermal conductivity - Google Patents
Composite foams of low thermal conductivityInfo
- Publication number
- CA2056918A1 CA2056918A1 CA002056918A CA2056918A CA2056918A1 CA 2056918 A1 CA2056918 A1 CA 2056918A1 CA 002056918 A CA002056918 A CA 002056918A CA 2056918 A CA2056918 A CA 2056918A CA 2056918 A1 CA2056918 A1 CA 2056918A1
- Authority
- CA
- Canada
- Prior art keywords
- foam
- particles
- thermal conductivity
- low thermal
- volume
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000006260 foam Substances 0.000 title claims abstract description 28
- 239000002131 composite material Substances 0.000 title claims abstract description 8
- 239000002245 particle Substances 0.000 claims abstract description 24
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000004965 Silica aerogel Substances 0.000 claims abstract description 8
- 239000000654 additive Substances 0.000 claims abstract description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 2
- 239000011872 intimate mixture Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 230000002209 hydrophobic effect Effects 0.000 claims 1
- 239000004964 aerogel Substances 0.000 description 13
- WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical compound COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 description 7
- 239000004604 Blowing Agent Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010097 foam moulding Methods 0.000 description 2
- 239000000017 hydrogel Substances 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 101150085091 lat-2 gene Proteins 0.000 description 1
- -1 lubrican~s Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- CMXPERZAMAQXSF-UHFFFAOYSA-M sodium;1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate;1,8-dihydroxyanthracene-9,10-dione Chemical group [Na+].O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O.CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC CMXPERZAMAQXSF-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/35—Composite foams, i.e. continuous macromolecular foams containing discontinuous cellular particles or fragments
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
- C08K7/26—Silicon- containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2201/00—Foams characterised by the foaming process
- C08J2201/02—Foams characterised by the foaming process characterised by mechanical pre- or post-treatments
- C08J2201/038—Use of an inorganic compound to impregnate, bind or coat a foam, e.g. waterglass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
-
- 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
- Y10S521/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S521/919—Sintered product
Abstract
0. 2 . 0050/4204g Abstract of the Disclosure: A. composite foam of low thermal conductivity comprises a) 20 80% by volume of silica aerogel particles having a mean diameter of from 0.1 to 20 mm and a density of from 0 . 08 to 0 .40 g/cm3, b) 20 - 80% by volume of a styrene polymer foam which surrounds the particles of component a) and binds them to one another and has a density of from 0 . 01 to 0.15 g/cm3, and, if desired, c) conventional additives in effective amount.
Description
20~6918 O.Z. 0~0/4~049 Compo~ita_fo~ms of low thermal conductivity ~he present invention relate~ to novel compo~ite foam~ which compri~e ~ilica aerogel particles and styrene polymer foam~ and are di~tinguiYhed by low thermal conductivity.
Convantional insulating material~ ba~ed on polyolefin~ and polyurethane~ are generally produced using organic blowing agent3, such as chlorofluoro-carbon~. The blowing agent included in the calls of the foam i3 xesponsibl~ for the high tharmal in ~lation capacity. Blowing agent~ of thi~ type are environm~ntal pollutant~ ~ince they 510wly Pscapa into the atmo~phere.
It is furthermora known that silica aerogels have an excellent th~rmal in~ulation capa ity. However, the product cannot be produced in a~y de~ired shapQ. It furthermore ha~ only low compressive strength and i~
susceptible to frac~uring. In addition, a loose aerogel pilè tends ~o ~hrink somewhat in volume due to gradual po~t-compreesion.
EP-A 340 707 proposes binding ~ilica a~rogel particle~ to ~orm compres~ion-resistant insulating material~ by means of an inorganic or organic binder.
However, the thermal conductivi~y of the~ product~ i8 unsa~i~factory.
It i3 an ob~ect of the pre~ent invention to d~velop ~n~ulating material3 havin~ a high thermal insulation capacity which are free fro~ environmentally unacceptable organic blowing agents.
It i8 a further ob~ect of the pre~ent inqention, in particular, to produce in3ulating materials of any desired shaps starting fxom ~ilica aerogel and at the ~ame time ~o compensate for the low compressive ~tr~ngth and high ~u~ceptibi}ity toward frac~ure of the aerogel and tha ~hrinkags in volume of an aerogel pile by binding thi~ substance into a matrix, while retaining the low thermal conductivity.
Convantional insulating material~ ba~ed on polyolefin~ and polyurethane~ are generally produced using organic blowing agent3, such as chlorofluoro-carbon~. The blowing agent included in the calls of the foam i3 xesponsibl~ for the high tharmal in ~lation capacity. Blowing agent~ of thi~ type are environm~ntal pollutant~ ~ince they 510wly Pscapa into the atmo~phere.
It is furthermora known that silica aerogels have an excellent th~rmal in~ulation capa ity. However, the product cannot be produced in a~y de~ired shapQ. It furthermore ha~ only low compressive strength and i~
susceptible to frac~uring. In addition, a loose aerogel pilè tends ~o ~hrink somewhat in volume due to gradual po~t-compreesion.
EP-A 340 707 proposes binding ~ilica a~rogel particle~ to ~orm compres~ion-resistant insulating material~ by means of an inorganic or organic binder.
However, the thermal conductivi~y of the~ product~ i8 unsa~i~factory.
It i3 an ob~ect of the pre~ent invention to d~velop ~n~ulating material3 havin~ a high thermal insulation capacity which are free fro~ environmentally unacceptable organic blowing agents.
It i8 a further ob~ect of the pre~ent inqention, in particular, to produce in3ulating materials of any desired shaps starting fxom ~ilica aerogel and at the ~ame time ~o compensate for the low compressive ~tr~ngth and high ~u~ceptibi}ity toward frac~ure of the aerogel and tha ~hrinkags in volume of an aerogel pile by binding thi~ substance into a matrix, while retaining the low thermal conductivity.
2~6~1~
- 2 - O . Z . 0050/420d~9 We have found that this ob~ect i~ achieved by a com3E?o8ite foam compri~ing ~ilica aerogel particles and styrene polymer foam~.
The invention accordingly provide~ a compo~ite foam of low thennal conducti~rity, compri~ing a) 20 - 80~6 by volume of ~ilica aerogel particle~
hav~ ng a mean diameter of from 0 .1 to 20 mm and density of from 0.08 to 0.40 g/cm3, b) 20 - 80% by volume of a styrene polymer foam whioh surrounds the particle~ of component a) and binds them to one another and h~ a den~ity o~ fro3r 0 . 01 to O .15 g/cm3~ and, if dehired, c: ) conventional additive~ in ef fective amount~ ~
The presant invention furthermore provide~ a.
process for the production of composite foams of thi~
type which compri~es heating an intimate mixtuxe of ~ilica aerogel particles and ~tyrene polymer foam par-ticles to a temperature above the so~tening point o~ th~3 ~tyrene pol~ner in a mold which clo~ not sQal in a ga~-tigh~ manner.
The e~ential constituent of the novel composite foam compri~e~ silica aerogel particles which hava a mean diameter o from 0.1 to 20 mm, preferably from 0.5 to 5 mm, in par~icular from 1 to 4 ~m.
The ~ilica aerogel particle~ are generally in the form of bead~ or ~ph~re and have a den~ity of from 0.05 to 0.40 g/cm3~ preferably from 0.08 to 0.35 q/cm3~ and a bulk density of from 0.04 to 0.25 gic~3 . Their thermal conductivity ~ i~ from 0.020 to ~.025 tW/m R].
The ~ilica aerogQl particles 9~8~ntially compri~e amo~phou~ S1O2 and contain traces of water and possibly small amounts of organic compounds (up to 10%), depending on the way in which they sre produced. They are produced in a conventional manner ~rom a water-glass ~olution via a sillca hydrogel by solven~ exchange and sub~equent drying. Thc bead form is produced by praying a rapidly gelling silicic acid 301 from a specially de~igned nozzle 2~6~8 - 3 - O.Z. 0~50/42049 and gelling the drops in ~he air. Further d~tail~ on thi~
proce~3 are given in D~-A 21 03 243. Replacement of the hydrogel wa~er by other liquid~ which are chemically inert toward SiO2 is de~cribed, for example, in VS-~
2,093,454, US-A 3,977,993 and JA-A 53/025,295, and the drying of the lyogels i~ described, for example, in ~S-A
2,093,454, US-A 2,249,767, FR-A 130 417, US-A 3,672,833, EP-A 0 018 955, US-A 4,327,065, EP-.A 0 067 741, DE-A
34 29 b71, EP A 0 186 149 and US-A 4,610,863. The gal liquid used for sup~rcritical d~ying i~ advantageou~ly dry mathanol, which mean~ that the ra~ultant aerogels are hydxophobic with an organic carbon content of about S~.
In the novel composite foams, the ~ilica aerogel particle~ are bound to one Another by a styrene polymer foam which ha~ 2 den~ity o~ from 0.01 to 0.15 g/cm3~
preferably from 0.015 to 0.09 g/cm3~ in particular from 0~02 to 0.07 g/~3.
~or the purpo~o3 of the pre~en~ invention, ~tyrene polymsr~ are poly~tyrene and copol~me.r~ o~
~tyrene which contain at least 50% by weight, preferab:ly at 18a8t 80% by wsight, of copolymerized styrene.
Examples of suitable comonomer~ are a-methyl~tyrene, ring-halogenated styrene~, ring-al~ylated ~tyrenes, acrylonitrile, e~ter~ of (meth)acrylic acid with alcohols having from 1 to 8 carbon atoms~ N-vinyl compounds~ such as ~inylcarbazole, maleic anhydride or alternatively sma}l ~mou~t~ of compound~ which contain two poly-merizable doubl~ bond~, such as bu~adiene, divinylbenzene or hutanediul diacrylate.
~he novel cempo~ite foam~ may furthermore contain con~entional additiva~ i~ effective amounts, such as dye3, pigment~, filler~, flameproofing agent~, ~ynergist~
for flameproofing agent~, antistatic~, stabilizers, lubrican~s, opacifier~ and the like. ~he addLtive~ may be both in the aerogel pha~e and in the foam phase.
The compo~ite foams are e~pediently produced by hea~iny an intimate mixture of silica aerogel particles 2~6318 - 4 - O.Z. ~05~/42049 and styrene polymer foam particle~ to a temperature above tha 90ftening point of the styrene pulymer in a mold which doe~ not se~l in a ga~-tight manner. Foam particl3s having a particle diameter o~ from 0.2 to 5 ~m, advanta-geou~ly from 0.25 to 4 mm, in particular from 0.3 to 3 mm, are ad~antageously u3ed. A particularly high molding quality and good welding iB achieved if at least ome of the foam particles are smaller than the inter-connecting cavit~a~ of khe aerogel particle material.
On heating, advantageou~ly by mean~ o ~team or hot air~ the ~yren~ polymer ~of~en~, ~he foam par~icle3 expand, and the pres~ure thi~ caus~ ~ub~tantially fill9 ~he interconnecting ca~itias with the fosm, and the foam surrounds the a~rogel par~icle~ to fonm a ~trong com-.
po~ite. After cooling, the composite foam molding i~
removed from the mold and dried if necessary. ~olding~
produced in a block mold can be cut into heets u~ing a suitable cutting device.
EXAMPLES
The amounts by volume shown in the Table of finely div$ded paxticle~ o expanded poly~tyrene and hydrophoblcized silica aerogel particles ara mixed in~imately and in~roduced into a mold wh~ch does not ~eal in a gas-t$ght manner, a~ i~ cu~tomary for the production of polystyrene foam molding~. ~he mold i8 flu~hed with steam (1 bar, 100C) for 15 second~ ~fter 10 minutesl the molding ean be ramov~d and i~ ~ub~equ~n~ly dried at 40C ~or 24 hours. The results are ~hown in the Table.
- S - O. Z . 0050/4~û49 . .
~ U~o u~ ~ O ~
~ _~ o _, ~ ~ .
o ~D O S:~
U~
U~o C~
o o~ ~ o o ~
o o o U~
U~ ~ o ,~, o ~o ~
o o ,1 ~ ", o n o c, U~
_I I o ~ P M O
~ ~~ ,1~ 0 0 O
I~
r~
~ U ~I
o ~ u ~. 8 8 ~ ~
U~
o o ~ ~ ~ Z;
a ~ ~ ~ w ~ ~ ~ ~ p ~ ~ ~ o .P~ O 3 O ~ U I ~ o ~ ~ ~o ~P ~ ~
o ~ I ~ ~ ~ ~ ~ Y ~ ~
W ~ ~ ~ ~ I ~ ~ ~ ~ ~ U
o ~ o ~ ~ ~ ~ ~ ~ ~ o ~ P U~ ~ ~
o~ Ul 0 O.~ ~ - o o ~ U ~ ~ ~ ~
(~ 0 (D 0 ~~rl P~ 1 C!~ --i o U~ H X ~--1 . I J~ ~ a u a I ~U a; 5 U:~ I '~
~ U ~ Xp" ~ s~ 1~
C~ m ~ ~ U ~
- 6 - O. Z . 0050/42049 . .
U~
C~
F~j J ,~ I I O I ~ I ~ O
O
C~
U~O .~) U~ O ~
O I I I~ ~1 1 1 1 1 ~ I
O
U~
~ L~ ~ ~ ~ O ~ ~a n CO ~ -~ O ~` ~ ~ O ,~
~ ~~D ~ O O
O
C~ O 1` ~ 0 Ul ~ O ~ C~
C` ~ O ~ O ~
t~~,0 1` 0 0 O
~D ~ O ~ ~ ~ O _~
U~ O
O ,_ _. ,-, ~
~ 0 U -i o u ~ o o a a~
u~ U tU
h ~ S~
. u H t~
~ a ,3 ~ a~ _~
h u~ I o ~ ~ ~ ~1 æ ,, ~ ~ ~ ~ ~ p ~ ~ P~
.~ u, ~ c~ ~ a o ~ o ~ U ~ U~ C~ U
w ca ~ ~ O ~ P Q~
. I P1 :~ O ~ O ~ A ~1 u 7:~ 0 I Y.l ~ ~ ~ ~ ~ ~ ~ 1 I o . 1 o ~ a~ ~ 1 0 ~ p U'~
llO m ~ 1 --~ O O h ~ ,1 ~
S ~ $~1 G ~ ~ ~ P~ co Z; X
_1 ,~ JJ ~ ~ ~ ~ ~60 ~ ~ ~ 0 0 a~
Q~ ~ ~ ua O ~rl ~rl ~rl tq ~ u h R h 13 , y e ~ ~ ., ~ ~o ~ ~ .. ~ 0 ~ ~
u~ c~
`~ o ~ o a ~ u c~ ~ a w E4 .1 u
- 2 - O . Z . 0050/420d~9 We have found that this ob~ect i~ achieved by a com3E?o8ite foam compri~ing ~ilica aerogel particles and styrene polymer foam~.
The invention accordingly provide~ a compo~ite foam of low thennal conducti~rity, compri~ing a) 20 - 80~6 by volume of ~ilica aerogel particle~
hav~ ng a mean diameter of from 0 .1 to 20 mm and density of from 0.08 to 0.40 g/cm3, b) 20 - 80% by volume of a styrene polymer foam whioh surrounds the particle~ of component a) and binds them to one another and h~ a den~ity o~ fro3r 0 . 01 to O .15 g/cm3~ and, if dehired, c: ) conventional additive~ in ef fective amount~ ~
The presant invention furthermore provide~ a.
process for the production of composite foams of thi~
type which compri~es heating an intimate mixtuxe of ~ilica aerogel particles and ~tyrene polymer foam par-ticles to a temperature above the so~tening point o~ th~3 ~tyrene pol~ner in a mold which clo~ not sQal in a ga~-tigh~ manner.
The e~ential constituent of the novel composite foam compri~e~ silica aerogel particles which hava a mean diameter o from 0.1 to 20 mm, preferably from 0.5 to 5 mm, in par~icular from 1 to 4 ~m.
The ~ilica aerogel particle~ are generally in the form of bead~ or ~ph~re and have a den~ity of from 0.05 to 0.40 g/cm3~ preferably from 0.08 to 0.35 q/cm3~ and a bulk density of from 0.04 to 0.25 gic~3 . Their thermal conductivity ~ i~ from 0.020 to ~.025 tW/m R].
The ~ilica aerogQl particles 9~8~ntially compri~e amo~phou~ S1O2 and contain traces of water and possibly small amounts of organic compounds (up to 10%), depending on the way in which they sre produced. They are produced in a conventional manner ~rom a water-glass ~olution via a sillca hydrogel by solven~ exchange and sub~equent drying. Thc bead form is produced by praying a rapidly gelling silicic acid 301 from a specially de~igned nozzle 2~6~8 - 3 - O.Z. 0~50/42049 and gelling the drops in ~he air. Further d~tail~ on thi~
proce~3 are given in D~-A 21 03 243. Replacement of the hydrogel wa~er by other liquid~ which are chemically inert toward SiO2 is de~cribed, for example, in VS-~
2,093,454, US-A 3,977,993 and JA-A 53/025,295, and the drying of the lyogels i~ described, for example, in ~S-A
2,093,454, US-A 2,249,767, FR-A 130 417, US-A 3,672,833, EP-A 0 018 955, US-A 4,327,065, EP-.A 0 067 741, DE-A
34 29 b71, EP A 0 186 149 and US-A 4,610,863. The gal liquid used for sup~rcritical d~ying i~ advantageou~ly dry mathanol, which mean~ that the ra~ultant aerogels are hydxophobic with an organic carbon content of about S~.
In the novel composite foams, the ~ilica aerogel particle~ are bound to one Another by a styrene polymer foam which ha~ 2 den~ity o~ from 0.01 to 0.15 g/cm3~
preferably from 0.015 to 0.09 g/cm3~ in particular from 0~02 to 0.07 g/~3.
~or the purpo~o3 of the pre~en~ invention, ~tyrene polymsr~ are poly~tyrene and copol~me.r~ o~
~tyrene which contain at least 50% by weight, preferab:ly at 18a8t 80% by wsight, of copolymerized styrene.
Examples of suitable comonomer~ are a-methyl~tyrene, ring-halogenated styrene~, ring-al~ylated ~tyrenes, acrylonitrile, e~ter~ of (meth)acrylic acid with alcohols having from 1 to 8 carbon atoms~ N-vinyl compounds~ such as ~inylcarbazole, maleic anhydride or alternatively sma}l ~mou~t~ of compound~ which contain two poly-merizable doubl~ bond~, such as bu~adiene, divinylbenzene or hutanediul diacrylate.
~he novel cempo~ite foam~ may furthermore contain con~entional additiva~ i~ effective amounts, such as dye3, pigment~, filler~, flameproofing agent~, ~ynergist~
for flameproofing agent~, antistatic~, stabilizers, lubrican~s, opacifier~ and the like. ~he addLtive~ may be both in the aerogel pha~e and in the foam phase.
The compo~ite foams are e~pediently produced by hea~iny an intimate mixture of silica aerogel particles 2~6318 - 4 - O.Z. ~05~/42049 and styrene polymer foam particle~ to a temperature above tha 90ftening point of the styrene pulymer in a mold which doe~ not se~l in a ga~-tight manner. Foam particl3s having a particle diameter o~ from 0.2 to 5 ~m, advanta-geou~ly from 0.25 to 4 mm, in particular from 0.3 to 3 mm, are ad~antageously u3ed. A particularly high molding quality and good welding iB achieved if at least ome of the foam particles are smaller than the inter-connecting cavit~a~ of khe aerogel particle material.
On heating, advantageou~ly by mean~ o ~team or hot air~ the ~yren~ polymer ~of~en~, ~he foam par~icle3 expand, and the pres~ure thi~ caus~ ~ub~tantially fill9 ~he interconnecting ca~itias with the fosm, and the foam surrounds the a~rogel par~icle~ to fonm a ~trong com-.
po~ite. After cooling, the composite foam molding i~
removed from the mold and dried if necessary. ~olding~
produced in a block mold can be cut into heets u~ing a suitable cutting device.
EXAMPLES
The amounts by volume shown in the Table of finely div$ded paxticle~ o expanded poly~tyrene and hydrophoblcized silica aerogel particles ara mixed in~imately and in~roduced into a mold wh~ch does not ~eal in a gas-t$ght manner, a~ i~ cu~tomary for the production of polystyrene foam molding~. ~he mold i8 flu~hed with steam (1 bar, 100C) for 15 second~ ~fter 10 minutesl the molding ean be ramov~d and i~ ~ub~equ~n~ly dried at 40C ~or 24 hours. The results are ~hown in the Table.
- S - O. Z . 0050/4~û49 . .
~ U~o u~ ~ O ~
~ _~ o _, ~ ~ .
o ~D O S:~
U~
U~o C~
o o~ ~ o o ~
o o o U~
U~ ~ o ,~, o ~o ~
o o ,1 ~ ", o n o c, U~
_I I o ~ P M O
~ ~~ ,1~ 0 0 O
I~
r~
~ U ~I
o ~ u ~. 8 8 ~ ~
U~
o o ~ ~ ~ Z;
a ~ ~ ~ w ~ ~ ~ ~ p ~ ~ ~ o .P~ O 3 O ~ U I ~ o ~ ~ ~o ~P ~ ~
o ~ I ~ ~ ~ ~ ~ Y ~ ~
W ~ ~ ~ ~ I ~ ~ ~ ~ ~ U
o ~ o ~ ~ ~ ~ ~ ~ ~ o ~ P U~ ~ ~
o~ Ul 0 O.~ ~ - o o ~ U ~ ~ ~ ~
(~ 0 (D 0 ~~rl P~ 1 C!~ --i o U~ H X ~--1 . I J~ ~ a u a I ~U a; 5 U:~ I '~
~ U ~ Xp" ~ s~ 1~
C~ m ~ ~ U ~
- 6 - O. Z . 0050/42049 . .
U~
C~
F~j J ,~ I I O I ~ I ~ O
O
C~
U~O .~) U~ O ~
O I I I~ ~1 1 1 1 1 ~ I
O
U~
~ L~ ~ ~ ~ O ~ ~a n CO ~ -~ O ~` ~ ~ O ,~
~ ~~D ~ O O
O
C~ O 1` ~ 0 Ul ~ O ~ C~
C` ~ O ~ O ~
t~~,0 1` 0 0 O
~D ~ O ~ ~ ~ O _~
U~ O
O ,_ _. ,-, ~
~ 0 U -i o u ~ o o a a~
u~ U tU
h ~ S~
. u H t~
~ a ,3 ~ a~ _~
h u~ I o ~ ~ ~ ~1 æ ,, ~ ~ ~ ~ ~ p ~ ~ P~
.~ u, ~ c~ ~ a o ~ o ~ U ~ U~ C~ U
w ca ~ ~ O ~ P Q~
. I P1 :~ O ~ O ~ A ~1 u 7:~ 0 I Y.l ~ ~ ~ ~ ~ ~ ~ 1 I o . 1 o ~ a~ ~ 1 0 ~ p U'~
llO m ~ 1 --~ O O h ~ ,1 ~
S ~ $~1 G ~ ~ ~ P~ co Z; X
_1 ,~ JJ ~ ~ ~ ~ ~60 ~ ~ ~ 0 0 a~
Q~ ~ ~ ua O ~rl ~rl ~rl tq ~ u h R h 13 , y e ~ ~ ., ~ ~o ~ ~ .. ~ 0 ~ ~
u~ c~
`~ o ~ o a ~ u c~ ~ a w E4 .1 u
Claims (3)
1. A composite foam of low thermal conductivity, comprising a) 20 - 80% by volume of Silica aerogel particles having a mean diameter of from 0.1 to 20 mm and a density of from 0.08 to 0.40 g/cm3, b) 20 - 80% by volume of a styrene polymer foam which surrounds the particles of component a) and binds them to one another and has a density of from 0.01 to 0.15 g/cm3, and, if desired, c) conventional additive in effective amounts.
2. A composite foam as claimed in claim 1, wherein the silica aerogel particles are hydrophobic.
3. A process for the production of a compotion foam as claimed in claim 1, which comprises heating an intimate mixture of silica aerogel particle and styrene polymer foam particles to a temperature above the soft ning point of the styrene polymer in a mold which does not seal in a gas-tight manner.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4038784A DE4038784A1 (en) | 1990-12-05 | 1990-12-05 | COMPOSITE FOAMS WITH LOW HEAT CONDUCTIVITY |
DEP4038784.4 | 1990-12-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2056918A1 true CA2056918A1 (en) | 1992-06-06 |
Family
ID=6419650
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002056918A Abandoned CA2056918A1 (en) | 1990-12-05 | 1991-12-04 | Composite foams of low thermal conductivity |
Country Status (9)
Country | Link |
---|---|
US (2) | US5124364A (en) |
EP (1) | EP0489319B2 (en) |
JP (1) | JPH04275344A (en) |
KR (1) | KR920012236A (en) |
AT (1) | ATE134682T1 (en) |
AU (1) | AU640066B2 (en) |
CA (1) | CA2056918A1 (en) |
DE (2) | DE4038784A1 (en) |
ES (1) | ES2083504T5 (en) |
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-
1990
- 1990-12-05 DE DE4038784A patent/DE4038784A1/en not_active Withdrawn
-
1991
- 1991-11-19 KR KR1019910020580A patent/KR920012236A/en not_active Application Discontinuation
- 1991-11-23 EP EP91119991A patent/EP0489319B2/en not_active Expired - Lifetime
- 1991-11-23 ES ES91119991T patent/ES2083504T5/en not_active Expired - Lifetime
- 1991-11-23 DE DE59107464T patent/DE59107464D1/en not_active Expired - Fee Related
- 1991-11-23 AT AT91119991T patent/ATE134682T1/en active
- 1991-12-02 US US07/801,289 patent/US5124364A/en not_active Expired - Lifetime
- 1991-12-04 CA CA002056918A patent/CA2056918A1/en not_active Abandoned
- 1991-12-04 JP JP3320164A patent/JPH04275344A/en not_active Withdrawn
- 1991-12-04 AU AU88389/91A patent/AU640066B2/en not_active Ceased
-
1992
- 1992-01-24 US US07/825,356 patent/US5137927A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
AU8838991A (en) | 1992-06-11 |
DE4038784A1 (en) | 1992-06-11 |
AU640066B2 (en) | 1993-08-12 |
KR920012236A (en) | 1992-07-25 |
EP0489319A2 (en) | 1992-06-10 |
DE59107464D1 (en) | 1996-04-04 |
EP0489319B2 (en) | 1999-04-14 |
ES2083504T5 (en) | 1999-07-01 |
ATE134682T1 (en) | 1996-03-15 |
EP0489319B1 (en) | 1996-02-28 |
EP0489319A3 (en) | 1993-03-31 |
JPH04275344A (en) | 1992-09-30 |
US5137927A (en) | 1992-08-11 |
US5124364A (en) | 1992-06-23 |
ES2083504T3 (en) | 1996-04-16 |
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