JPH01101321A - Heat insulator - Google Patents

Heat insulator

Info

Publication number
JPH01101321A
JPH01101321A JP62258857A JP25885787A JPH01101321A JP H01101321 A JPH01101321 A JP H01101321A JP 62258857 A JP62258857 A JP 62258857A JP 25885787 A JP25885787 A JP 25885787A JP H01101321 A JPH01101321 A JP H01101321A
Authority
JP
Japan
Prior art keywords
polyol
heat insulator
catalyst
thermal conductivity
synthesized
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.)
Pending
Application number
JP62258857A
Other languages
Japanese (ja)
Inventor
Noritake Sumida
憲武 隅田
Hidekazu Kai
甲斐 英一
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sharp Corp
Original Assignee
Sharp Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sharp Corp filed Critical Sharp Corp
Priority to JP62258857A priority Critical patent/JPH01101321A/en
Publication of JPH01101321A publication Critical patent/JPH01101321A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02BCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
    • Y02B40/00Technologies aiming at improving the efficiency of home appliances, e.g. induction cooking or efficient technologies for refrigerators, freezers or dish washers

Landscapes

  • Refrigerator Housings (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 く技術分野〉 本発明は冷蔵庫等に利用する断熱体に関するものである
DETAILED DESCRIPTION OF THE INVENTION Technical Field The present invention relates to a heat insulator used in refrigerators and the like.

〈従来技術〉 近年、冷蔵庫のニーズは大容量の方向に進んでいる度面
、外形寸法は住宅事情等から設置スペースに限界があり
、冷蔵庫の内容積と外容積の比率いわゆる容積効率の高
いものが求められてお9断熱体の薄壁化が重要な課題と
なっている。
<Prior art> In recent years, the need for refrigerators has been moving toward larger capacity, but there are limits to the installation space due to housing conditions, etc., and the ratio of internal volume to external volume of refrigerators is high. As a result, making the walls of the insulation body thinner has become an important issue.

一般的に冷蔵庫の断熱体には硬質ポリウレタンフォーム
が使用されておりその原料処方はショ糖系、芳香族ジア
ミン系をベースにしたポリエーテルポリオール、アミン
系触媒、シリコン系整泡剤および発泡剤R−11を有機
イソシアネートで重合度広させたものである。
Generally, rigid polyurethane foam is used for the insulation of refrigerators, and its raw material formulation is sucrose-based, aromatic diamine-based polyether polyol, amine catalyst, silicone-based foam stabilizer, and foaming agent R. -11 with an organic isocyanate to increase the degree of polymerization.

最近では断熱性能を向上させるためにポリエーテルポリ
オールの一部をポリエステルポリオールあるいはペン゛
シリツクエーテル系フェノールにおきかえる処方も考え
られている。
Recently, formulations in which part of the polyether polyol is replaced with polyester polyol or pensilicate phenol have been considered in order to improve the heat insulation performance.

錨 〈  が解決しようとする問題点〉    ・このよう
な断熱体においてはポリオールのy応活性が十分でない
之め有機イソシアネートとの反応初期においてセルが微
細化せず断熱体の熱伝導率が十分に小さくならないとい
う欠点があった。
Anchor〈Problems to be solved〉 ・In such a heat insulator, the polyol does not have sufficient y-reactive activity, so the cells do not become fine in the early stage of the reaction with the organic isocyanate, and the thermal conductivity of the heat insulator does not reach a sufficient level. The drawback was that it did not become smaller.

本発明は上記問題点に鑑み優れた断熱性能が得られる断
熱体を提供することを目的としている。
SUMMARY OF THE INVENTION In view of the above-mentioned problems, an object of the present invention is to provide a heat insulator that provides excellent heat insulation performance.

く問題点を解決するための手段〉 ゛本発明はポリオール成分に有機金属触媒を用いて合成
したポリエステルポリオールを30重量%以下添加する
ことによりポリオールの反応活性を高くし熱伝導率の小
さい断熱体を得る。
Means for Solving the Problems〉 〛The present invention increases the reaction activity of the polyol by adding 30% by weight or less of polyester polyol synthesized using an organometallic catalyst to the polyol component, thereby creating a heat insulating material with low thermal conductivity. get.

〈作 用〉 本発明は上記の如くポリオール成分に有機金属触媒を用
いて合成したポリエステルポリオ−/L/を添加するこ
とによフ、有機イソシアネートのうちTDIのバラ位の
イソシアネート基とポリエステルポリオールがすみやか
に反応するため反応初期にセルが微細化し、熱伝導率の
十分に小さい断熱体を得ることができる。
<Function> As described above, in the present invention, by adding polyester polyol/L/ synthesized using an organometallic catalyst to the polyol component, the isocyanate group at the rose position of TDI in the organic isocyanate and the polyester polyol are combined. Because the reaction occurs quickly, the cells become finer in the early stage of the reaction, making it possible to obtain a heat insulator with sufficiently low thermal conductivity.

〈実施例〉 以下本発明の一実施例を図ならびに表に基づいて説明す
る。
<Example> An example of the present invention will be described below based on figures and tables.

表において、ポリオールAは芳香族ジアミン系、ショ糖
系の水酸基価45’ Om g KOH/gのポリエー
テルポリオール、ポリオ−1vBは通常の方法で合成さ
れたフタル酸エステル系の水酸基価400mgKOH/
gのポリエステルポリオール、ポリオ−pcは有機金属
触媒を用いて合成したフタル酸エステル系の水酸基価4
00mgKOH/gのポリエステルポリオールである。
In the table, Polyol A is an aromatic diamine-based, sucrose-based polyether polyol with a hydroxyl value of 45' Omg KOH/g, and Polyol-1vB is a phthalate-based polyether polyol synthesized by a conventional method with a hydroxyl value of 400 mg KOH/g.
The polyester polyol of g, POLY-PC, is a phthalate ester polyol synthesized using an organometallic catalyst and has a hydroxyl value of 4.
00mgKOH/g polyester polyol.

整泡剤はシリコン系界面活性剤1.5部、発泡剤はフロ
ンR−11、触媒はアミン系あるいは有機金属触媒であ
り、発泡剤および触媒の量は断熱材の密度仄応性を同一
にするため原料処方によυ調整を行なった。有機イソシ
アネートは粗−TDI  TDIプレポリマー混合物(
アミン当i135 )と粗MDI(アミン当量135)
を重量比70 : 30に混合したものである。これら
の原料を種々組合せてパネル発泡を行ないその一部を実
施例として黒1〜5を表わした。
The foam stabilizer is 1.5 parts of a silicone surfactant, the blowing agent is Freon R-11, and the catalyst is an amine-based or organometallic catalyst, and the amounts of the blowing agent and catalyst are set so that the density responsiveness of the insulation material is the same. Therefore, υ was adjusted according to the raw material formulation. Organic isocyanate is crude TDI TDI prepolymer mixture (
i135 per amine) and crude MDI (amine equivalent 135)
were mixed in a weight ratio of 70:30. Panel foaming was carried out using various combinations of these raw materials, and some of them were used as examples to represent blacks 1 to 5.

得られた硬質ポリウレタンフォームの熱伝導率は昭和電
工調熱伝導率計QTMを用いて平均温度32℃で測定し
た。
The thermal conductivity of the obtained rigid polyurethane foam was measured at an average temperature of 32° C. using a Showa Denko thermal conductivity meter QTM.

表から明らかなようにポリオ−/L/(、すなわち有機
金属触媒を用いて合成したポリエステルポリオールを添
加した処方& 4 、 /15はポリオールBすなわち
触媒を使用しない通常の方法で合成したポリエステルポ
リオールを添加した処方点2.煮3と比較して熱伝導率
の小さい断熱体が得られた。
As is clear from the table, polyol B/L/(i.e., a formulation containing a polyester polyol synthesized using an organometallic catalyst) is polyol B, i.e., a polyester polyol synthesized by a conventional method without using a catalyst. A heat insulator with a lower thermal conductivity was obtained compared to the added recipe point 2 and 3.

これはポリオールCの反応活性が高くなっており、有機
イソシアネートとの反応がすみやかにおこり、反応初期
においてセルが微細化するためと考えられる。
This is considered to be because the reaction activity of polyol C is high, and the reaction with the organic isocyanate occurs quickly, resulting in finer cells in the initial stage of the reaction.

図はポリオール成分中に添加するポリオールCの量を変
化させて、1次数#1(脱型後、室温での収縮)ならび
に熱伝導率の関係について種々の発泡試験により求めた
結果である。1次収縮率は室温で24時間後、熱伝導率
は平均温度32℃で測定を行なった。この図から明らか
なようにポリオ−/L/co添加量を増加させるに従っ
て収縮率は大きくなるが、熱伝導率はポリオール成分中
に15部以上添那してもほぼ一定の傾向にあることがわ
かる。これはポリオールCの添加量を増加するに従って
ポリオ−A/Cと粗MDIの結合が増加するため機械的
強度が小さくなり、断熱体の強度が低下し、1次収縮が
大きくなると考えられる。一方、熱伝導率は有機イソシ
アネートとポリオールの反応初期の段階におけるセルの
状態に大きく左右されるすなわち本発明の実施例ではポ
リオールCと粗TDIバラ位のイソシナネート基の反応
に影響を受ける。従ってポリオールCの水酸基と粗TD
Iバラ位のイソシアネート基の当量比が1以上になって
も熱伝導率は大きく変化しないものと考えられる。
The figure shows the results obtained by various foaming tests on the relationship between linear number #1 (shrinkage at room temperature after demolding) and thermal conductivity by varying the amount of polyol C added to the polyol component. The primary shrinkage rate was measured after 24 hours at room temperature, and the thermal conductivity was measured at an average temperature of 32°C. As is clear from this figure, the shrinkage rate increases as the amount of polyol/L/co added increases, but the thermal conductivity tends to remain almost constant even when 15 parts or more is added to the polyol component. Recognize. It is thought that this is because as the amount of polyol C added increases, the bond between polyol-A/C and crude MDI increases, resulting in a decrease in mechanical strength, a decrease in the strength of the heat insulator, and an increase in primary shrinkage. On the other hand, the thermal conductivity is greatly influenced by the state of the cell at the initial stage of the reaction between the organic isocyanate and the polyol, that is, in the examples of the present invention, it is influenced by the reaction between polyol C and the isocyanate group at the distal position of the crude TDI. Therefore, the hydroxyl group of polyol C and the crude TD
It is considered that even if the equivalent ratio of the isocyanate group at the I-position becomes 1 or more, the thermal conductivity does not change significantly.

なお、本発明は上記実施例に限定されるものではなく、
触媒、整泡剤、ポリオール成分などを調整することによ
り、より優れた断熱性能を有する断熱体を得ることも可
能である。
Note that the present invention is not limited to the above embodiments,
By adjusting the catalyst, foam stabilizer, polyol component, etc., it is also possible to obtain a heat insulator with better heat insulation performance.

〈効 果〉 本発明は、以上の如くポリオール、有機イソシアネート
、触媒、整泡剤および発泡剤を用いて得られる硬質ポリ
ウレタンフォーム断熱体において、上記ポリオール成分
に有機金属触媒を用いて合成したポリエステルポリオー
ルを30重量Φ以下含有したことを特徴とする断熱体に
関するものであるから、1次収縮の少さい優れた断熱性
能を有する断熱体が得られるという顕著な効果を奏し得
る図面はポリエステルポリオール(ポリオールC)の含
有量と1次収縮率、熱伝導率の関係を示す図である。
<Effects> The present invention provides a rigid polyurethane foam heat insulating material obtained using a polyol, an organic isocyanate, a catalyst, a foam stabilizer, and a foaming agent as described above, in which a polyester polyol synthesized using an organometallic catalyst as the polyol component is used. Since this relates to a heat insulating body characterized by containing 30 weight Φ or less of polyester polyol (polyol It is a figure showing the relationship between the content of C), the primary shrinkage rate, and the thermal conductivity.

Claims (1)

【特許請求の範囲】[Claims] 1、ポリオール、有機イソシアネート、触媒、整泡剤お
よび発泡剤を用いて得られる硬質ポリウレタンフォーム
断熱体において、上記ポリオール成分に有機金属触媒を
使用して合成したポリエステルポリオールを30重量%
以下含有したことを特徴とする断熱体。
1. In a rigid polyurethane foam insulation obtained using a polyol, an organic isocyanate, a catalyst, a foam stabilizer, and a foaming agent, 30% by weight of a polyester polyol synthesized using an organometallic catalyst is added to the above polyol component.
A heat insulator characterized by containing the following:
JP62258857A 1987-10-13 1987-10-13 Heat insulator Pending JPH01101321A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62258857A JPH01101321A (en) 1987-10-13 1987-10-13 Heat insulator

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62258857A JPH01101321A (en) 1987-10-13 1987-10-13 Heat insulator

Publications (1)

Publication Number Publication Date
JPH01101321A true JPH01101321A (en) 1989-04-19

Family

ID=17325998

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62258857A Pending JPH01101321A (en) 1987-10-13 1987-10-13 Heat insulator

Country Status (1)

Country Link
JP (1) JPH01101321A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0386735A (en) * 1989-08-31 1991-04-11 Mitsui Toatsu Chem Inc Production of thermal insulation material
JPH05500985A (en) * 1990-02-20 1993-02-25 ザ ダウ ケミカル カンパニー Rigid polyurethane foam with low thermal conductivity

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0386735A (en) * 1989-08-31 1991-04-11 Mitsui Toatsu Chem Inc Production of thermal insulation material
JPH05500985A (en) * 1990-02-20 1993-02-25 ザ ダウ ケミカル カンパニー Rigid polyurethane foam with low thermal conductivity

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