JPH0453891B2 - - Google Patents
Info
- Publication number
- JPH0453891B2 JPH0453891B2 JP11594885A JP11594885A JPH0453891B2 JP H0453891 B2 JPH0453891 B2 JP H0453891B2 JP 11594885 A JP11594885 A JP 11594885A JP 11594885 A JP11594885 A JP 11594885A JP H0453891 B2 JPH0453891 B2 JP H0453891B2
- Authority
- JP
- Japan
- Prior art keywords
- foam
- asphalt
- solution
- heating
- regeneration solution
- 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.)
- Expired - Lifetime
Links
- 239000006260 foam Substances 0.000 claims description 70
- 239000010426 asphalt Substances 0.000 claims description 52
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 24
- 230000008929 regeneration Effects 0.000 claims description 24
- 238000011069 regeneration method Methods 0.000 claims description 24
- 239000012948 isocyanate Substances 0.000 claims description 14
- 150000002513 isocyanates Chemical class 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 13
- 239000002131 composite material Substances 0.000 claims description 12
- 239000000295 fuel oil Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 8
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 7
- 239000011496 polyurethane foam Substances 0.000 claims description 7
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 239000000839 emulsion Substances 0.000 claims description 5
- 229910052806 inorganic carbonate Inorganic materials 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 229920005862 polyol Polymers 0.000 claims description 5
- 150000003077 polyols Chemical class 0.000 claims description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 238000005187 foaming Methods 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 32
- 238000000034 method Methods 0.000 description 15
- 238000005470 impregnation Methods 0.000 description 6
- 239000011259 mixed solution Substances 0.000 description 6
- 230000001172 regenerating effect Effects 0.000 description 6
- 238000009413 insulation Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- CVNKFOIOZXAFBO-UHFFFAOYSA-J tin(4+);tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Sn+4] CVNKFOIOZXAFBO-UHFFFAOYSA-J 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/141—Feedstock
- Y02P20/143—Feedstock the feedstock being recycled material, e.g. plastics
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/62—Plastics recycling; Rubber recycling
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
Description
【発明の詳細な説明】
〔発明の技術分野〕
本発明は発泡体シートを基材とし、その特性で
ある弾力性を適度に保持すると共に、優れた吸音
性、遮音性断熱性を具備させた複合材シートの製
造方法に関する。[Detailed Description of the Invention] [Technical Field of the Invention] The present invention uses a foam sheet as a base material, which maintains its characteristic elasticity to an appropriate level and has excellent sound absorption, sound insulation, and heat insulation properties. The present invention relates to a method for manufacturing a composite sheet.
発泡体シートを基材とした複合材シートの例と
しては、連続気泡を有するウレタンフオームに溶
融アスフアルトあるいはアスフアルトエマルジヨ
ンを含浸させることにより撥水性および緩徐な復
元力を付与したものが目地材等として従来広く用
いられている(以下、このようにアスフアルトの
撥水性と発泡体の復元力を備えたものをアスフア
ルトフオームという)。
An example of a composite sheet based on a foam sheet is a urethane foam with open cells impregnated with molten asphalt or asphalt emulsion to impart water repellency and slow restoring force, and can be used as a joint material, etc. It has been widely used in the past (hereinafter, a product with the water repellency of asphalt and the resilience of foam will be referred to as asphalt foam).
また、上記のアスフアルトフオームとは別に、
アスフアルトの水性エマルジヨンに、エチレンオ
キサイド含有率15%以上のポリエーテルポリオー
ルと有機イソシアネートとを反応させて得らたウ
レタンプレポリマーを添加混合して発泡させたア
スフアルトフオームが知られている。この製造方
法は本願の出願人が特願昭57−125373号として提
案したもので、前記含浸法と違つてアスフアルト
粒子が全体に均一に分散されるため均一な品質が
得られ、且つアスフアルト自体がフオーム基体を
構成しているため、アスフアルトがフオーム基体
から分離して品質の劣化を生じないという優れた
特長を有している。 In addition to the asphalt foam mentioned above,
Asphalt foam is known, which is formed by adding and mixing a urethane prepolymer obtained by reacting a polyether polyol with an ethylene oxide content of 15% or more with an organic isocyanate to an aqueous asphalt emulsion, and then foaming the mixture. This manufacturing method was proposed in Japanese Patent Application No. 57-125373 by the applicant of the present application, and unlike the above-mentioned impregnation method, the asphalt particles are uniformly dispersed throughout, resulting in uniform quality. Since it is composed of a foam base, it has the excellent feature that the asphalt does not separate from the foam base and cause quality deterioration.
更に、出願人は上記提案になるアスフアルトフ
オームの加工裁断屑や不良品の有効利用を目的と
し、これら不良品を溶融処理した再生溶液を連続
気泡のウレタンフオームに含浸することにより、
アスフアルトフオームを再生製造する方法を先に
提案した。こうして得られたアスフアルトフオー
ムの性質は、冒頭で説明した含浸法で製造された
ものに類似している。しかし、含浸される溶融物
がアスフアルト以外にウレタン成分を含有してい
るためウレタンフオームに対する親和性が良好
で、アスフアルト成分の分離滲み出しが比較的少
ない。 Furthermore, the applicant aims to make effective use of the asphalt foam processing waste and defective products proposed above, by impregnating open-cell urethane foam with a recycled solution obtained by melting these defective products.
We have previously proposed a method for remanufacturing asphalt foam. The properties of the asphalt foam thus obtained are similar to those produced by the impregnation method described at the beginning. However, since the impregnated melt contains a urethane component in addition to asphalt, it has good affinity for the urethane foam, and the asphalt component separates and seeps out relatively little.
上記各種のアスフアルトフオームは何れも目地
材に適した特性のみならず、吸音性や遮音性に優
れ、更に防震性をも具備することが明らかになつ
た。そのため、近年では自動車用のフロア材等、
防音防震特性を生かした用途で効果的に用いられ
ている。
It has become clear that all of the above-mentioned asphalt foams not only have properties suitable for joint materials, but also have excellent sound absorbing and sound insulating properties, as well as earthquake proofing properties. Therefore, in recent years, floor materials for automobiles, etc.
It is effectively used in applications that take advantage of its sound and earthquake insulation properties.
しかし、吸音性および遮音性を大きくするため
にアスフアルト成分の含有浸量を多くすると、弾
力性が著しく低下する問題があつた。また、含浸
溶液の粘度調節が困難で、特にアスフアルトを多
量に含浸したい場合には、粘度が高くなつて均一
な含浸が難しく、含浸ムラを生じる問題があつ
た。 However, when the amount of asphalt component is increased in order to increase the sound absorption and sound insulation properties, there is a problem in that the elasticity is significantly reduced. Further, it is difficult to control the viscosity of the impregnating solution, and especially when a large amount of asphalt is desired to be impregnated, the viscosity becomes high, making it difficult to uniformly impregnate the solution, resulting in uneven impregnation.
本発明は上記事情に鑑みてなされたもので、発
泡体基材中にアスフアルト成分を均一に含浸する
ことができ、且つ製品に適度の弾力性を付与する
ことができる複合材の製造方法を提供するもので
ある。
The present invention has been made in view of the above circumstances, and provides a method for manufacturing a composite material that can uniformly impregnate an asphalt component into a foam base material and impart appropriate elasticity to the product. It is something to do.
本発明による複合材の製造方法は、エチレンオ
キサイド含有率15%以上のポリエーテルポリオー
ルと有機イソシアネートとの反応で生成したウレ
タンプレポリマーをアスフアルトの水性エマルジ
ヨン中に添加混合して発泡させることにより得ら
れたアスフアルトフオームに無機炭酸塩を添加し
て一緒に加熱し、溶解することによりアスフアル
トフオームの再生溶液を調製する工程と、アミン
系触媒および/または錫系触媒を添加した溶媒中
にポリウレタンフオームを加え、加熱、撹拌して
溶解することによりウレタンフオーム再生溶液を
調製する工程と、該ウレタンフオーム再生溶液、
前記アスフアルトフオーム再生溶液および重油の
混合液を連続気泡を有する発泡体シートに適量含
浸させた後、有機イソシアネートを含浸させ加
熱、硬化させる工程とを具備したことを特徴とす
るものである。
The method for producing a composite material according to the present invention is to add and mix a urethane prepolymer produced by a reaction between a polyether polyol having an ethylene oxide content of 15% or more and an organic isocyanate into an aqueous emulsion of asphalt, and then foam the composite material. A step of preparing a regenerated solution of asphalt foam by adding an inorganic carbonate to the asphalt foam and heating and dissolving the same; and a step of adding polyurethane foam to a solvent containing an amine-based catalyst and/or a tin-based catalyst. , a step of preparing a urethane foam regeneration solution by heating, stirring and dissolving; the urethane foam regeneration solution;
The method is characterized by comprising the steps of impregnating an appropriate amount of a mixed solution of the asphalt foam regenerating solution and heavy oil into a foam sheet having open cells, impregnating it with an organic isocyanate, and heating and curing it.
本発明の別の製造方法は、上記の製造方法にお
いて、有機イソシアネートを後から別に含浸させ
ることなく、アスフアルトフオーム再生溶液、ウ
レタンフオーム再生溶液および重油と一緒に混合
して同時に含浸させるものである。 Another production method of the present invention is the above production method, in which the organic isocyanate is mixed together with the asphalt foam regeneration solution, urethane foam regeneration solution, and heavy oil and impregnated at the same time, without separately impregnating the organic isocyanate afterwards.
上記本発明による製造方法を、出願人が先に提
案したアスフアルトフオーム再生溶液のみを含浸
させる方法とを比較すると、ウレタンフオーム再
生溶液および重油を混合して含浸させる点で異な
つている。以下に本発明の詳細を説明する。 When the manufacturing method according to the present invention is compared with the method previously proposed by the applicant in which only an asphalt foam regeneration solution is impregnated, the difference is that the urethane foam regeneration solution and heavy oil are mixed and impregnated. The details of the present invention will be explained below.
本発明においてアスフアルトフオームの再生溶
液を調製する工程には、出願人が特願昭59−
200668号として先に提案した方法が利用されてい
る。この方法では炭酸カルシウム、炭酸ナトリウ
ム、炭酸マグネシウム、炭酸バリウム等の無機炭
酸塩を添加して一緒に加熱するが、その添加比率
はアスフアルトフオーム100重量部に対して炭酸
塩0.5〜20重量部である。これら無機炭酸塩を添
加することにより、アスフアルトフオームの溶融
に要する加熱時間を略1/2に短縮できる。 In the present invention, the step of preparing a regenerating solution of asphalt foam is carried out by the applicant in the patent application filed in
The method previously proposed as No. 200668 is used. In this method, inorganic carbonates such as calcium carbonate, sodium carbonate, magnesium carbonate, barium carbonate, etc. are added and heated together, and the addition ratio is 0.5 to 20 parts by weight of carbonate per 100 parts by weight of asphalt foam. . By adding these inorganic carbonates, the heating time required for melting the asphalt foam can be reduced to about half.
本発明においてウレタンフオームの再生溶液を
調製する工程にも、出願人が先に提案した方法
(特願昭59−176190号等)が利用されている。こ
の場合、ウレタンフオームを溶解するための溶液
としては、例えばポリヒドロキシ化合物や燐酸エ
ステル系可塑剤を用いることができる。これらの
溶媒中に塩化錫、水酸化錫、酸化錫、錫地金等を
触媒として添加し、この中にウレタンフオームを
加えて加熱溶解することにより、ポリウレタンリ
ンケージが切断され、再度の重合反応および発泡
反応を行なう能力を有する再生溶液が得られる。
本発明において、このウレタンフオーム再生溶液
は最終製品に適度な弾力性を付与するために前記
アスフアルトフオーム再生溶液に混合されるもの
である。その混合比率はアスフアルトフオーム再
生溶液100重量部に対し、20〜200重量部が好まし
い。 In the present invention, the method previously proposed by the applicant (Japanese Patent Application No. 59-176190, etc.) is also used in the step of preparing the urethane foam regeneration solution. In this case, as a solution for dissolving the urethane foam, for example, a polyhydroxy compound or a phosphoric acid ester plasticizer can be used. Tin chloride, tin hydroxide, tin oxide, tin metal, etc. are added as a catalyst to these solvents, and urethane foam is added thereto and heated to dissolve, thereby cutting the polyurethane linkage and allowing another polymerization reaction and A regeneration solution is obtained which has the ability to carry out a foaming reaction.
In the present invention, this urethane foam regeneration solution is mixed with the asphalt foam regeneration solution in order to impart appropriate elasticity to the final product. The mixing ratio is preferably 20 to 200 parts by weight per 100 parts by weight of the asphalt foam regeneration solution.
本発明においてアスフアルトフオーム再生溶液
中に重油を混合する理由は、含浸溶液の粘度を調
整するためである。その混合比率はアスフアルト
フオーム再生溶液100重量部に対し、15〜75重量
部が好ましい。 The reason why heavy oil is mixed into the asphalt foam regeneration solution in the present invention is to adjust the viscosity of the impregnation solution. The mixing ratio thereof is preferably 15 to 75 parts by weight per 100 parts by weight of the asphalt foam regenerating solution.
本発明で用いる有機イソシアネートとしては、
4,4−ジフエニルメタンジイソシアネート、ト
リレンジイソシアネート等のイソシアネート単体
でもよいし、また末端NCO基をもつウレタンプ
レポリマーでもよい。 As the organic isocyanate used in the present invention,
It may be a single isocyanate such as 4,4-diphenylmethane diisocyanate or tolylene diisocyanate, or it may be a urethane prepolymer having a terminal NCO group.
本発明で用いる連続気泡を有する発泡体シート
としては、ウレタンフオームシートが最適である
が、連続気泡の発泡体であればウレタンフオーム
以外の発泡体シートを使用してもよい。また、そ
の厚さは任意でよいが、一般には5mm〜30mmのも
のを用いる。 As the foam sheet having open cells used in the present invention, a urethane foam sheet is most suitable, but any foam sheet other than urethane foam may be used as long as it is an open cell foam. Further, the thickness may be arbitrary, but generally 5 mm to 30 mm is used.
本発明の実施に際しては、上記アスフアルトフ
オーム再生溶液、ウレタンフオーム再生溶液およ
び重油を混合し、この混合液を上記の連続気泡を
有する発泡体シートに含浸させる。その際、含浸
溶液には重油が添加されているため粘度が低く、
均一且つ容易に含浸することができる。含浸方法
としては浴槽による浸漬法、スプレー法、或いは
転写法等を使用できる。その際、混合含浸液を50
℃〜150℃程度に加熱しておくと粘度が更に著し
く低下し、含浸し易くなる。この粘度調節のため
の加熱が容易であることから、転写法または浸漬
法によるものが特に好ましい。こうして混合溶液
を含浸させた後、前記有機イソシアネートを含浸
させて加熱すると、有機イソシアネートがアスフ
アルトフオーム再生溶液やウレタンフオーム再生
溶液中に含まれていた成分と反応し、重合硬化し
て所期の複合材が得られる。 In carrying out the present invention, the above-mentioned asphalt foam regeneration solution, urethane foam regeneration solution, and heavy oil are mixed, and the above-mentioned open-cell foam sheet is impregnated with this mixed liquid. At that time, the viscosity is low because heavy oil is added to the impregnation solution.
Can be impregnated uniformly and easily. As the impregnation method, a dipping method using a bathtub, a spray method, a transfer method, etc. can be used. At that time, add 50% of the mixed impregnating liquid.
If heated to about 150°C to 150°C, the viscosity will further decrease significantly, making it easier to impregnate. Since heating for adjusting the viscosity is easy, a method using a transfer method or a dipping method is particularly preferable. After impregnating the mixed solution in this way, the organic isocyanate is impregnated and heated, and the organic isocyanate reacts with the components contained in the asphalt foam regeneration solution and the urethane foam regeneration solution, and polymerizes and hardens to form the desired composite. wood is obtained.
こうして製造された複合材は、従来のアスフア
ルトフオーム同様に優れた吸音性および遮音性を
具備し、また止水性にも優れている。更に、有機
イソシアネートの重合反応によつて適度な弾力性
が付与されている。 The composite material manufactured in this manner has excellent sound absorption and sound insulation properties similar to conventional asphalt foam, and also has excellent water-stopping properties. Furthermore, appropriate elasticity is imparted through the polymerization reaction of organic isocyanate.
以下に本発明の実施例を説明する。 Examples of the present invention will be described below.
(1) まず、アスフアルトフオームを打抜き加工す
る際に形成された打抜き屑を粉砕機にて細片化
し、その200gをステンレス容器内に計量した。
これに炭酸カルシウム20gとアスフアルト100
gとを加え、220℃に加熱撹拌したところ、ア
スフアルトフオームが液状に溶融した。続い
て、温度を220℃に維持しながら更に少しずつ
アスフアルトフオームの細片を加え、何等支障
なく合計1000gのアスフアルトフオームを溶解
し、アスフアルトフオーム再生溶液を得た。(1) First, punching waste formed when asphalt foam was punched was cut into pieces using a crusher, and 200 g of the pieces were weighed into a stainless steel container.
Add to this 20g of calcium carbonate and 100 asphalt.
When the mixture was heated and stirred at 220° C., the asphalt foam melted into a liquid state. Subsequently, while maintaining the temperature at 220° C., small pieces of asphalt foam were added little by little, and a total of 1000 g of asphalt foam was dissolved without any problem, thereby obtaining an asphalt foam regenerating solution.
(2) 上記とは別に、分子量3000,3官能のポリエ
ーテルポリオール700gと、ジブチルチンジラ
ウレート15gと、陽イオン界面活性剤および第
4級アンモニウム塩の合計5gとを夫々計量し
てステンレス容器中に混合した。続いて、加熱
ヒータを用いてこの溶液を加熱しながら、その
中に軟質ポリウレタンフオームの細片1000gを
少しづつ添加して溶解させた。最終的な温度は
200℃であつた。(2) Separately from the above, weigh 700 g of a trifunctional polyether polyol with a molecular weight of 3000, 15 g of dibutyltin dilaurate, and a total of 5 g of a cationic surfactant and a quaternary ammonium salt and place them in a stainless steel container. Mixed. Subsequently, while heating this solution using a heater, 1000 g of soft polyurethane foam strips were added little by little and dissolved therein. The final temperature is
It was 200℃.
こうして得られたポリウレタンフオームの再
生溶液は、常温下において粘度の高い液体であ
つた。 The polyurethane foam regeneration solution thus obtained was a highly viscous liquid at room temperature.
(3) 上記のようにして調整されたアスフアルトフ
オーム再生溶液100重量部に対し、ポリウレタ
ンフオーム再生溶液30重量部を加えて温度120
℃で撹拌混合した。続いて、アスフアルトフオ
ーム再生溶液100重量部に対して40重量部の比
率で重油を添加し、撹拌して混合液を得た。(3) To 100 parts by weight of the asphalt foam regenerating solution prepared as above, add 30 parts by weight of the polyurethane foam regenerating solution and
The mixture was stirred and mixed at ℃. Subsequently, heavy oil was added at a ratio of 40 parts by weight to 100 parts by weight of the asphalt foam regeneration solution and stirred to obtain a mixed solution.
次いで、この混合液を80℃に加熱しておき、そ
の中に厚さ10mmの軟質ポリウレタンフオームシー
トを浸漬して混合液を含浸させ、更に絞りロール
を通過させることにより、混合液の含浸量をポリ
ウレタンフオーム100重量部に対して700重量部に
なるように調整した。その後、スプレーにより
4,4′−ジフエニルメタンジイソシアネートを吹
きつけ、押圧ロールにて含浸させてオーブン中に
導入し、120℃で7分観加熱キユアーさせて複合
材を製造した。 Next, this mixed solution was heated to 80°C, and a 10 mm thick flexible polyurethane foam sheet was immersed in it to impregnate it with the mixed solution.The amount of the mixed solution impregnated was then reduced by passing it through a squeezing roll. The amount was adjusted to 700 parts by weight based on 100 parts by weight of the polyurethane foam. Thereafter, 4,4'-diphenylmethane diisocyanate was sprayed onto the surface, impregnated with a pressure roll, and introduced into an oven, followed by heating and curing at 120 DEG C. for 7 minutes to produce a composite material.
こうして得られた複合材は、吸音性および遮音
性に優れると共に、適度の弾力性を有していた。 The composite material thus obtained had excellent sound absorbing and sound insulating properties, as well as moderate elasticity.
以上詳述したように、本発明によれば発泡体基
材中にアスフアルト成分を均一に含浸した複合材
を製造することができ、且つ製品に適度の弾力性
を付与することができる等、顕著な効果が得られ
るものである。
As detailed above, according to the present invention, it is possible to produce a composite material in which the asphalt component is uniformly impregnated into the foam base material, and it is also possible to impart appropriate elasticity to the product. It is possible to obtain the following effects.
Claims (1)
ーテルポリオールと有機イソシアネートとの反応
で生成したウレタンプレポリマーをアスフアルト
の水性エマルジヨン中に添加混合して発泡させる
ことにより得られたアスフアルトフオームに無機
炭酸塩を添加して一緒に加熱し、溶解することに
よりアスフアルトフオームの再生溶液を調製する
工程と、アミン系触媒および/または錫系触媒を
添加した溶媒中にポリウレタンフオームを加え、
加熱、撹拌して溶解することによりウレタンフオ
ーム再生溶液を調製する工程と、該ウレタンフオ
ーム再生溶液、前記アスフアルトフオーム再生溶
液および重油の混合液を連続気泡を有する発泡体
シートに適量含浸させた後、有機イソシアネート
を含浸させ加熱、硬化させる工程とを具備したこ
とを特徴とする複合材の製造方法。 2 エチレンオキサイド含有率15%以上のポリエ
ーテルポリオールと有機イソシアネートとの反応
で生成したウレタンプレポリマーをアスフアルト
の水性エマルジヨン中に添加混合して発泡させる
ことにより得られたアスフアルトフオームに無機
炭酸塩を添加して一緒に加熱し、溶解することに
よりアスフアルトフオームの再生溶液を調製する
工程と、アミン系触媒および/または錫系触媒を
添加した溶媒中にポリウレタンフオームを加え、
加熱、撹拌して溶解することによりウレタンフオ
ーム再生溶液を調製する工程と、該ウレタンフオ
ーム再生溶液と前記アスフアルトフオーム再生溶
液と重油と有機イソシアネートとの混合液を連続
気泡を有する発泡体シートに適量含浸させた後、
加熱、硬化させる工程とを具備したことを特徴と
する複合材の製造方法。[Claims] 1. Asphalt foam obtained by adding and mixing a urethane prepolymer produced by the reaction of a polyether polyol having an ethylene oxide content of 15% or more with an organic isocyanate into an aqueous asphalt emulsion and foaming the mixture. A step of preparing a regenerated solution of asphalt foam by adding an inorganic carbonate to the mixture and heating and dissolving the same, and adding polyurethane foam into a solvent containing an amine-based catalyst and/or a tin-based catalyst;
A step of preparing a urethane foam regeneration solution by heating, stirring and dissolving it, and impregnating an appropriate amount of the mixture of the urethane foam regeneration solution, the asphalt foam regeneration solution and heavy oil into a foam sheet having open cells, 1. A method for producing a composite material, comprising the steps of impregnating the material with an organic isocyanate, heating and curing the material. 2 Adding an inorganic carbonate to an asphalt foam obtained by adding and mixing a urethane prepolymer produced by a reaction between a polyether polyol with an ethylene oxide content of 15% or more and an organic isocyanate into an aqueous asphalt emulsion and foaming the mixture. preparing a regenerated solution of asphalt foam by heating and dissolving the asphalt foam together;
A step of preparing a urethane foam regeneration solution by dissolving it by heating and stirring, and impregnating an appropriate amount of a mixture of the urethane foam regeneration solution, the asphalt foam regeneration solution, heavy oil, and organic isocyanate into a foam sheet having open cells. After letting
A method for producing a composite material, comprising the steps of heating and curing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60115948A JPS61272250A (en) | 1985-05-29 | 1985-05-29 | Production of composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60115948A JPS61272250A (en) | 1985-05-29 | 1985-05-29 | Production of composite material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61272250A JPS61272250A (en) | 1986-12-02 |
| JPH0453891B2 true JPH0453891B2 (en) | 1992-08-27 |
Family
ID=14675122
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60115948A Granted JPS61272250A (en) | 1985-05-29 | 1985-05-29 | Production of composite material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61272250A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5252641A (en) * | 1990-02-21 | 1993-10-12 | Institut Francais Du Petrole | Process for production of bituminous compositions containing polymeric residues |
| FR2658524B1 (en) * | 1990-02-21 | 1992-05-15 | Inst Francais Du Petrole | BITUMINOUS COMPOSITIONS CONTAINING RESIDUES OF THERMOPLASTIC POLYMERS WITH POLYURETHANE FOAMS AND THERMOSET RESINS, AS WELL AS THEIR PREPARATION PROCESS. |
-
1985
- 1985-05-29 JP JP60115948A patent/JPS61272250A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61272250A (en) | 1986-12-02 |
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