CN111909355A - Fatigue-resistant low-density high-resilience sponge and preparation method thereof - Google Patents

Fatigue-resistant low-density high-resilience sponge and preparation method thereof Download PDF

Info

Publication number
CN111909355A
CN111909355A CN202010811222.7A CN202010811222A CN111909355A CN 111909355 A CN111909355 A CN 111909355A CN 202010811222 A CN202010811222 A CN 202010811222A CN 111909355 A CN111909355 A CN 111909355A
Authority
CN
China
Prior art keywords
fatigue
resistant low
component
resilience sponge
density high
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
CN202010811222.7A
Other languages
Chinese (zh)
Inventor
柴可军
荆晓东
王帅
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.)
ZIBO ZHENGDA POLYURETHANE Co.,Ltd.
Original Assignee
荆晓东
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 荆晓东 filed Critical 荆晓东
Priority to CN202010811222.7A priority Critical patent/CN111909355A/en
Publication of CN111909355A publication Critical patent/CN111909355A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4829Polyethers containing at least three hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/161Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
    • C08G18/163Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22 covered by C08G18/18 and C08G18/22
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/161Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
    • C08G18/163Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22 covered by C08G18/18 and C08G18/22
    • C08G18/165Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22 covered by C08G18/18 and C08G18/22 covered by C08G18/18 and C08G18/24
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/18Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/1808Catalysts containing secondary or tertiary amines or salts thereof having alkylene polyamine groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/18Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/1825Catalysts containing secondary or tertiary amines or salts thereof having hydroxy or primary amino groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/18Catalysts containing secondary or tertiary amines or salts thereof
    • C08G18/20Heterocyclic amines; Salts thereof
    • C08G18/2009Heterocyclic amines; Salts thereof containing one heterocyclic ring
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/22Catalysts containing metal compounds
    • C08G18/222Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/22Catalysts containing metal compounds
    • C08G18/24Catalysts containing metal compounds of tin
    • C08G18/242Catalysts containing metal compounds of tin organometallic compounds containing tin-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/22Catalysts containing metal compounds
    • C08G18/26Catalysts containing metal compounds of lead
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/63Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
    • C08G18/632Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers onto polyethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/721Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
    • C08G18/722Combination of two or more aliphatic and/or cycloaliphatic polyisocyanates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7614Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/79Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/791Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention belongs to the field of chemical industry, and particularly relates to a fatigue-resistant low-density high-resilience sponge and a preparation method thereof. The fatigue-resistant low-density high-resilience sponge has low density and extremely strong fatigue resistance, has good flame-retardant property compared with the high-resilience sponge directly foamed by TDI, increases the indentation performance of the sponge on the basis of not damaging the resilience rate, is a good material for seats of automobile drivers and movie theaters, provides better comfortable hand feeling and touch feeling for passengers, and reduces fatigue caused by long-time sitting.

Description

Fatigue-resistant low-density high-resilience sponge and preparation method thereof
Technical Field
The invention belongs to the field of chemical industry, and particularly relates to a fatigue-resistant low-density high-resilience sponge and a preparation method thereof.
Background
The polyurethane foam is gradually and rapidly developed since the industrialization of the last 50 century, and is widely applied to various fields, in particular to seat cushions, back cushions, headrests, sound-absorbing and shock-absorbing cushions and the like of transportation vehicles such as cars, passenger cars, airplanes and the like and movie theaters. Because of higher rebound resilience and comfort, the passenger can feel comfortable and the fatigue of riding is reduced.
In recent years, due to the development trend of light weight of automobiles and the demand of reducing production cost of automobile main engine plants, automobile seat manufacturers have increasingly proposed the requirement of reducing the density of high-resilience foam, the fatigue resistance of high-resilience sponge is weak, and the elongation and tear strength of low-density high-resilience sponge are lost.
Disclosure of Invention
According to the defects of the prior art, the invention provides the fatigue-resistant low-density high-resilience sponge and the preparation method thereof, the TDI trimer solution with very good thermal stability is added into the system, the catalyst more suitable for high-resilience molding sponge is selected, and the polyether polyol newly developed by the applicant is adopted, so that the high-resilience foam has flame retardance, and the sponge keeps the resilience effect and the indentation performance of the sponge at low density.
The invention relates to a fatigue-resistant low-density high-resilience sponge, which comprises the following components in part by weight: the component A and the component B are mixed according to the mass ratio of 100: 30-45, preparing;
the component A is prepared from polyether polyol, polymer polyol and an auxiliary agent according to a mass ratio of 100: 40-80: 25-35;
the component B is polyisocyanate.
Furthermore, the polyether polyol is polyether polyol DEP-3033, a 3-functionality polyether polyol with molecular weight of 4000-6000 produced by Zibodexin Federal chemical industry Limited.
Furthermore, the polymer polyol is polymer polyol H45, and the solid content of the polymer polyol produced by Zibode Federal chemical industry Co., Ltd is 38-45%.
Furthermore, the auxiliary agent comprises, by weight, 1-5% of a metal catalyst, 5-15% of an amine catalyst, 3-10% of a cross-linking agent, 10-20% of a foaming agent, 35-50% of a flame retardant, 10-20% of a pore-forming agent and 2-8% of a foam stabilizer.
Furthermore, the metal catalyst is at least one of zinc isooctanoate, lead isooctanoate and dibutyltin dilaurate; the amine catalyst is at least one of N, N, N ', N' -tetraethyl methane diamine, N-ethyl morpholine, N, N, N ', N' -tetramethyl propylamine and DMEA (dimethyl ethanolamine); at least one of the crosslinking agents DETDA (diethyl toluene diamine), DMTDA (dimethyl sulfur toluene diamine) and triisopropanolamine; the foaming agent is water; the flame retardant is at least one of DDMP (2, 3-dihydro-3, 5 dihydroxy-6-methyl-4 (H) -pyran-4-one) and DMMP (dimethyl methylphosphonate); the pore-forming agent is at least one of ECOADD 3360 and ALLCHEM 3350 (Shanghai-Lengxing industries, Ltd.); the foam stabilizer is at least one of B8681 (German winning-Chuang Gaussmeter), B-5064 (Shanghai Baion chemical technology Co., Ltd.), KPS-1251 (Spanish Peixi Co., Ltd.).
Furthermore, the polyisocyanate is prepared from TDI and TDI trimer according to a mass ratio of 100: 15-35 by mixing.
The invention also provides a preparation method of the fatigue-resistant low-density high-resilience sponge, which comprises the following steps: controlling the temperature to be 25 +/-2 ℃, stirring and mixing the component A and the component B, pouring the mixture into a mold at 50-60 ℃ for molding and foaming, demolding after 5min, and standing the prepared foam for 72h to obtain the fatigue-resistant low-density high-resilience sponge.
The invention has the advantages that:
(1) the TDI tripolymer solution is added, and the tripolymer has an isocyanurate six-membered ring structure, so that the structure has very good thermal stability, the thermal decomposition temperature of the structure is 377 ℃, and the isocyanurate structure is introduced into the polyurethane material, so that the flame retardance of the foam can be effectively improved;
(2) the catalyst more suitable for the high-resilience molding sponge is selected, and the newly developed polyether polyol is adopted, so that the sponge keeps the resilience effect and the indentation performance of the sponge when in low density, and the high-resilience molding sponge is used as a good material for seats of automobile drivers and movie theaters, provides better comfortable hand feeling and touch feeling for passengers, and reduces fatigue caused by long-time sitting.
Detailed Description
The present invention is further illustrated by the following examples.
Example 1:
a fatigue-resistant low-density high-resilience sponge is prepared from a component A and a component B according to the mass ratio of 100: 30, preparing the raw materials;
the component A is prepared from polyether polyol DEP-3033, polymer polyol H45 and an auxiliary agent according to the mass ratio of 100: 50: 25;
the auxiliary agent comprises, by weight, 1% of a metal catalyst, 15% of an amine catalyst, 3% of a cross-linking agent, 20% of a foaming agent, 35% of a flame retardant, 20% of a cell opening agent and 6% of a foam stabilizer. Wherein the metal catalyst is zinc isooctanoate; the amine catalyst is N-ethyl morpholine; the cross-linking agent is triisopropanolamine; the foaming agent is water, and the flame retardant is DDMP; the pore former is ALLCHEM 3350 (Bright and Bright practical Co., Ltd.); the foam stabilizer was KPS-1251 (Peixi Spanish).
The component B is prepared from TDI and TDI tripolymer according to the mass ratio of 100: 15 are mixed together.
During preparation, the temperature is controlled to be 25 +/-2 ℃, the component A and the component B are stirred and mixed, then poured into a mold at 60 ℃ for molding and foaming, demolding is carried out after 5min, and the prepared foam is placed for 72h to obtain the fatigue-resistant low-density high-resilience sponge.
Example 2:
a fatigue-resistant low-density high-resilience sponge is prepared from a component A and a component B according to the mass ratio of 100: 40;
the component A is prepared from polyether polyol DEP-3033, polymer polyol H45 and an auxiliary agent according to the mass ratio of 100: 40: 35;
the auxiliary agent comprises 3% of metal catalyst, 10% of amine catalyst, 5% of cross-linking agent, 10% of foaming agent, 50% of flame retardant, 20% of pore-forming agent and 2% of foam stabilizer in percentage by weight, wherein the metal catalyst is lead isooctanoate; the amine catalyst is N, N, N ', N' -tetramethyl propylamine; the cross-linking agent is DETDA; the foaming agent is water, and the flame retardant is DMMP; the cell opener is ECOADD 3360 (Bright and practical Co., Ltd.); the foam stabilizer is B8681 (German winning-Chuanggauss meter).
The component B is prepared from TDI and TDI tripolymer according to the mass ratio of 100: 20 are mixed together.
During preparation, the temperature is controlled to be 25 +/-2 ℃, the component A and the component B are stirred and mixed, then poured into a mold at 55 ℃ for molding foaming, demolding is carried out after 5min, and the prepared foam is placed for 72h to obtain the fatigue-resistant low-density high-resilience sponge.
Example 3:
a fatigue-resistant low-density high-resilience sponge is prepared from a component A and a component B according to the mass ratio of 100: 45, preparing the raw materials;
the component A is prepared from polyether polyol DEP-3033, polymer polyol H45 and an auxiliary agent according to the mass ratio of 100: 70: 30;
the auxiliary agent comprises, by weight, 3% of a metal catalyst, 13% of an amine catalyst, 7% of a crosslinking agent, 20% of a foaming agent, 40% of a flame retardant, 10% of a pore-forming agent and 7% of a foam stabilizer, wherein the metal catalyst is dibutyltin dilaurate; the amine catalyst is N, N, N ', N' -tetraethyl methane diamine; the cross-linking agent is DMTDA; the foaming agent is water; the flame retardant is DDMP; the pore former is ALLCHEM 3350 (Bright and Bright practical Co., Ltd.); the foam stabilizer is B-5064 (Shanghai Baion chemical technology Co., Ltd.).
The component B is prepared from TDI and TDI tripolymer according to the mass ratio of 100: 25 are mixed together.
During preparation, the temperature is controlled to be 25 +/-2 ℃, the component A and the component B are stirred and mixed, then poured into a mold at 60 ℃ for molding and foaming, demolding is carried out after 5min, and the prepared foam is placed for 72h to obtain the fatigue-resistant low-density high-resilience sponge.
Example 4:
a fatigue-resistant low-density high-resilience sponge is prepared from a component A and a component B according to the mass ratio of 100: 40;
the component A is prepared from polyether polyol DEP-3033, polymer polyol H45 and an auxiliary agent according to the mass ratio of 100: 60: 30;
the auxiliary agent comprises, by weight, 4% of a metal catalyst, 10% of an amine catalyst, 6% of a cross-linking agent, 15% of a foaming agent, 45% of a flame retardant, 15% of a pore-forming agent and 5% of a foam stabilizer, wherein the metal catalyst is dibutyltin dilaurate; the amine catalyst is N, N, N ', N' -tetraethyl methane diamine; the cross-linking agent is DMTDA; the foaming agent is water; the flame retardant is DDMP; the pore former is ALLCHEM 3350 (Bright and Bright practical Co., Ltd.); the foam stabilizer is B-5064 (Shanghai Baion chemical technology Co., Ltd.).
The component B is prepared from TDI and TDI tripolymer according to the mass ratio of 100: 30 are mixed together.
During preparation, the temperature is controlled to be 25 +/-2 ℃, the component A and the component B are stirred and mixed, then poured into a mold at 50 ℃ for molding and foaming, demolding is carried out after 5min, and the prepared foam is placed for 72h to obtain the fatigue-resistant low-density high-resilience sponge.
Example 5:
a fatigue-resistant low-density high-resilience sponge is prepared from a component A and a component B according to the mass ratio of 100: 45, preparing the raw materials;
the component A is prepared from polyether polyol DEP-3033, polymer polyol H45 and an auxiliary agent according to the mass ratio of 100: 80: 38;
the auxiliary agent comprises, by weight, 5% of a metal catalyst, 7% of an amine catalyst, 10% of a cross-linking agent, 15% of a foaming agent, 45% of a flame retardant, 10% of a pore-forming agent and 8% of a foam stabilizer, wherein the metal catalyst is lead isooctanoate; the amine catalyst is DMEA; the cross-linking agent is DETDA; the foaming agent is water; the flame retardant is DDMP; the pore former is ALLCHEM 3350 (Bright and Bright practical Co., Ltd.); the foam stabilizer is B8681 (German winning-Chuanggauss meter).
The component B is prepared from TDI and TDI tripolymer according to the mass ratio of 100: 30 are mixed together.
During preparation, the temperature is controlled to be 25 +/-2 ℃, the component A and the component B are stirred and mixed, then poured into a mold at 55 ℃ for molding foaming, demolding is carried out after 5min, and the prepared foam is placed for 72h to obtain the fatigue-resistant low-density high-resilience sponge.
Test example:
a commercially available high-resilience sponge is taken as a comparative example, the foam is placed under a metal disc according to the standard GB/T18941-2003 with the high-resilience sponge prepared in the comparative example and the examples 1-5, and the dynamic fatigue resistance of the foam is examined by repeatedly impacting 8 ten thousand times under the pressure of 750N. As shown in Table 1, the indentation hardness was measured in GB/T10807-2006, the ball rebound was measured in GB/T6670-2008, and the oxygen index was measured in GB/T2406.2-2009, for 40% indentation hardness loss and foam thickness loss of the foam after 8 ten thousand impacts.
Table 1:
Figure BDA0002631029380000071
Figure BDA0002631029380000081
as seen from Table 1, examples 1 to 5 each had a lower 40-indentation hardness loss ratio and a lower thickness loss ratio than those of the comparative examples, and had a density of 20kg/m3When the alloy is used, the indentation hardness and the rebound resilience are similar to those of a comparative example, and the oxygen index is improved.

Claims (7)

1. The utility model provides a high resilience sponge of fatigue-resistant low density which characterized in that: the component A and the component B are mixed according to the mass ratio of 100: 30-45, preparing;
the component A is prepared from polyether polyol, polymer polyol and an auxiliary agent according to a mass ratio of 100: 40-80: 25-35;
the component B is polyisocyanate.
2. The fatigue-resistant low-density high-resilience sponge according to claim 1, wherein: the polyether polyol is polyether polyol DEP-3033, and is 3-functionality polyether polyol with molecular weight of 4000-6000 produced by ZibodeFederal chemical industry Limited.
3. The fatigue-resistant low-density high-resilience sponge according to claim 1, wherein: the polymer polyol is polymer polyol H45, and the solid content of the polymer polyol produced by ZibodeXin Federal chemical industry Limited is 38-45%.
4. The fatigue-resistant low-density high-resilience sponge according to claim 1, wherein: the auxiliary agent comprises, by weight, 1-5% of a metal catalyst, 5-15% of an amine catalyst, 3-10% of a cross-linking agent, 10-20% of a foaming agent, 35-50% of a flame retardant, 10-20% of a pore-forming agent and 2-8% of a foam stabilizer.
5. The fatigue-resistant low-density high-resilience sponge according to claim 4, wherein: the metal catalyst is at least one of zinc isooctanoate, lead isooctanoate and dibutyltin dilaurate; the amine catalyst is at least one of N, N, N ', N' -tetraethyl methane diamine, N-ethyl morpholine, N, N, N ', N' -tetramethyl propylamine and DMEA; at least one of the crosslinking agents DETDDA, DMTDA and triisopropanolamine; the foaming agent is water; the flame retardant is at least one of DDMP and DMMP; the pore-opening agent is at least one of ECOADD 3360 and ALLCHEM 3350; the foam stabilizer is at least one of B8681, B-5064 and KPS-1251.
6. The fatigue-resistant low-density high-resilience sponge according to claim 1, wherein: the polyisocyanate is prepared from TDI and TDI trimer according to the mass ratio of 100: 15-35 by mixing.
7. A preparation method of the fatigue-resistant low-density high-resilience sponge according to any one of claims 1 to 6, which is characterized by comprising the following steps: controlling the temperature to be 25 +/-2 ℃, stirring and mixing the component A and the component B, pouring the mixture into a mold at 50-60 ℃ for molding and foaming, demolding after 5min, and standing the prepared foam for 72h to obtain the fatigue-resistant low-density high-resilience sponge.
CN202010811222.7A 2020-08-13 2020-08-13 Fatigue-resistant low-density high-resilience sponge and preparation method thereof Pending CN111909355A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010811222.7A CN111909355A (en) 2020-08-13 2020-08-13 Fatigue-resistant low-density high-resilience sponge and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010811222.7A CN111909355A (en) 2020-08-13 2020-08-13 Fatigue-resistant low-density high-resilience sponge and preparation method thereof

Publications (1)

Publication Number Publication Date
CN111909355A true CN111909355A (en) 2020-11-10

Family

ID=73284471

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010811222.7A Pending CN111909355A (en) 2020-08-13 2020-08-13 Fatigue-resistant low-density high-resilience sponge and preparation method thereof

Country Status (1)

Country Link
CN (1) CN111909355A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112778486A (en) * 2021-01-08 2021-05-11 福建省天骄化学材料有限公司 High-density environment-friendly polymer polyol and preparation method and application thereof
CN113402693A (en) * 2021-06-29 2021-09-17 广州亚伊汽车零部件有限公司 Formula and preparation method of high-resilience foaming material
CN113416410A (en) * 2021-07-06 2021-09-21 佛山市协通橡塑制品有限公司 Running board and preparation method thereof
CN114106292A (en) * 2021-12-06 2022-03-01 甘肃银光聚银化工有限公司 Preparation method of high-load-bearing polyurethane flexible foam
CN115044014A (en) * 2022-05-16 2022-09-13 上海抚佳精细化工有限公司 Toluene diisocyanate prepolymer and preparation method and application thereof

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1329088A (en) * 1969-09-09 1973-09-05 Dunlop Holdings Ltd Polyurethane foams
CN1100030A (en) * 1993-09-10 1995-03-15 唐化学原料公司 Polyurethane foam moldings
JP2004346196A (en) * 2003-05-22 2004-12-09 Toyo Tire & Rubber Co Ltd Molded product of flexible polyurethane foam and method for producing the same
CN101031601A (en) * 2004-10-01 2007-09-05 拜尔材料科学有限公司 Molded flexible polyurethane foams with reduced flammability and superior durability
CN101205288A (en) * 2006-12-22 2008-06-25 比亚迪股份有限公司 Polyurethane foam compositions
CN101210066A (en) * 2006-12-30 2008-07-02 比亚迪股份有限公司 Entire polyurethane foam composition
CN101284902A (en) * 2007-03-14 2008-10-15 拜尔材料科学有限公司 Trimer and allophanate modified isocyanates, a process for their production, foams comprising these modified isocyanates, and a process for the production of these foams
CN102140159A (en) * 2010-11-26 2011-08-03 山东东大一诺威聚氨酯有限公司 Environmental-friendly combination material for cold curing slow rebound polyurethane foam and preparation method thereof
CN102321237A (en) * 2011-04-21 2012-01-18 南京红宝丽股份有限公司 Polylol for foamed plastic and polyisocyanurate foamed plastic adopting same
CN105111397A (en) * 2015-09-24 2015-12-02 江阴市向阳科技有限公司 Low-VOC (volatile organic compound) and high-resilience polyurethane foam mixed material and method for preparing same
CN106750169A (en) * 2016-12-21 2017-05-31 重庆德盈汽车零部件有限公司 A kind of high resilience polyurethane foam and preparation method thereof
CN107298749A (en) * 2017-05-25 2017-10-27 德清舒华泡沫座椅有限公司 A kind of urethane foam for use in automobile seats material and preparation method thereof
CN107987781A (en) * 2017-12-06 2018-05-04 苏州铂邦胶业有限公司 Polyurethane sealant
CN109232843A (en) * 2017-07-11 2019-01-18 重庆宏立至信科技发展集团股份有限公司 Low VOC, high rebound seat foam of low smell and preparation method thereof
CN110387025A (en) * 2019-08-01 2019-10-29 荆晓东 A kind of polyurethane steering wheel and preparation method thereof
CN110885417A (en) * 2019-11-22 2020-03-17 山东蓝星东大有限公司 Compression-resistant low-density TDI (toluene diisocynate) type high-resilience foam sponge and preparation method thereof

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1329088A (en) * 1969-09-09 1973-09-05 Dunlop Holdings Ltd Polyurethane foams
CN1100030A (en) * 1993-09-10 1995-03-15 唐化学原料公司 Polyurethane foam moldings
JP2004346196A (en) * 2003-05-22 2004-12-09 Toyo Tire & Rubber Co Ltd Molded product of flexible polyurethane foam and method for producing the same
CN101031601A (en) * 2004-10-01 2007-09-05 拜尔材料科学有限公司 Molded flexible polyurethane foams with reduced flammability and superior durability
CN101205288A (en) * 2006-12-22 2008-06-25 比亚迪股份有限公司 Polyurethane foam compositions
CN101210066A (en) * 2006-12-30 2008-07-02 比亚迪股份有限公司 Entire polyurethane foam composition
CN101284902A (en) * 2007-03-14 2008-10-15 拜尔材料科学有限公司 Trimer and allophanate modified isocyanates, a process for their production, foams comprising these modified isocyanates, and a process for the production of these foams
CN102140159A (en) * 2010-11-26 2011-08-03 山东东大一诺威聚氨酯有限公司 Environmental-friendly combination material for cold curing slow rebound polyurethane foam and preparation method thereof
CN102321237A (en) * 2011-04-21 2012-01-18 南京红宝丽股份有限公司 Polylol for foamed plastic and polyisocyanurate foamed plastic adopting same
CN105111397A (en) * 2015-09-24 2015-12-02 江阴市向阳科技有限公司 Low-VOC (volatile organic compound) and high-resilience polyurethane foam mixed material and method for preparing same
CN106750169A (en) * 2016-12-21 2017-05-31 重庆德盈汽车零部件有限公司 A kind of high resilience polyurethane foam and preparation method thereof
CN107298749A (en) * 2017-05-25 2017-10-27 德清舒华泡沫座椅有限公司 A kind of urethane foam for use in automobile seats material and preparation method thereof
CN109232843A (en) * 2017-07-11 2019-01-18 重庆宏立至信科技发展集团股份有限公司 Low VOC, high rebound seat foam of low smell and preparation method thereof
CN107987781A (en) * 2017-12-06 2018-05-04 苏州铂邦胶业有限公司 Polyurethane sealant
CN110387025A (en) * 2019-08-01 2019-10-29 荆晓东 A kind of polyurethane steering wheel and preparation method thereof
CN110885417A (en) * 2019-11-22 2020-03-17 山东蓝星东大有限公司 Compression-resistant low-density TDI (toluene diisocynate) type high-resilience foam sponge and preparation method thereof

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
化学工业出版社: "《中国化工产品大全》", 31 July 1994, 化学工业出版社 *
张利国等: "汽车座椅用高回弹泡沫撕裂强度影响因素研究*", 《聚氨酯工业》 *
方禹声: "《聚氨酯泡沫塑料 第2版》", 31 August 1994, 化学工业出版社 *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112778486A (en) * 2021-01-08 2021-05-11 福建省天骄化学材料有限公司 High-density environment-friendly polymer polyol and preparation method and application thereof
CN113402693A (en) * 2021-06-29 2021-09-17 广州亚伊汽车零部件有限公司 Formula and preparation method of high-resilience foaming material
CN113416410A (en) * 2021-07-06 2021-09-21 佛山市协通橡塑制品有限公司 Running board and preparation method thereof
CN114106292A (en) * 2021-12-06 2022-03-01 甘肃银光聚银化工有限公司 Preparation method of high-load-bearing polyurethane flexible foam
CN115044014A (en) * 2022-05-16 2022-09-13 上海抚佳精细化工有限公司 Toluene diisocyanate prepolymer and preparation method and application thereof
CN115044014B (en) * 2022-05-16 2024-05-17 上海抚佳精细化工有限公司 Toluene diisocyanate prepolymer and preparation method and application thereof

Similar Documents

Publication Publication Date Title
CN111909355A (en) Fatigue-resistant low-density high-resilience sponge and preparation method thereof
CN101392049B (en) All-MDI polyurethane low resilience urethane foam resilient foam
CN107857865B (en) Full-water environment-friendly flame-retardant flatulence memory polyurethane foam for automobile seat and preparation method thereof
CN101205288B (en) Polyurethane foam compositions
CN101096406B (en) Cold curing polyurethane high-resilience foam component material and preparation method thereof
CN101250253B (en) Formula of cold curing foam and forming technique
CN109320682B (en) Low-density high-resilience foam for automobile seat and preparation method thereof
CN106589309B (en) Automotive seat combines material and preparation method thereof with high-performance all-MDI polyurethane
CN111607061B (en) Flame retardant-free high-flame-retardance low-odor full-water self-skinning polyurethane foam and preparation method thereof
CN106046303A (en) Polyol composition for producing flexible polyurethane foam and flexible polyurethane foam
EP2089204A2 (en) Non-petroleum-based polyurethane foam products having improved performance specifications and method of production
CN111548475B (en) Slow-rebound memory cotton and preparation method thereof
JP6007204B2 (en) Polyurethane foam formulations, products, and methods
CN107298749A (en) A kind of urethane foam for use in automobile seats material and preparation method thereof
CN102633978A (en) Polyurethane foam and preparation method thereof
CA2861788A1 (en) Pressure-distributing foam and vehicle seat assembly having pressure-distributing foam
CN106117485A (en) A kind of ageing-resistant environment-protecting polyurethane foam composition material and preparation method thereof
CN116102709B (en) Polyurethane composite material for filling solid core of tire and preparation method and application thereof
CN111423555A (en) High-temperature-resistant and aging-resistant polyurethane foam and preparation method and application thereof
CN111647125A (en) Polyurethane composition and preparation of sponge product thereof
CN104204017A (en) Polyurethane foam for seat pad
WO2010051448A1 (en) Palm oil-based polyurethane foam products and method of production
CN113549193A (en) WJ-8A type high-speed rail elastic base plate with low-temperature static rigidity change rate
CN112552476A (en) Polyurethane foam material and preparation method thereof
CN114920981B (en) Polyurethane tire filler foamed by using expanded microspheres and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
TA01 Transfer of patent application right

Effective date of registration: 20210625

Address after: 255000 no.3482 Baoshan Road, high tech Zone, Zibo City, Shandong Province

Applicant after: ZIBO ZHENGDA POLYURETHANE Co.,Ltd.

Address before: 256410 Shihua Road, Guoli Town, Huantai County, Zibo City, Shandong Province

Applicant before: Jing Xiaodong

TA01 Transfer of patent application right
RJ01 Rejection of invention patent application after publication

Application publication date: 20201110

RJ01 Rejection of invention patent application after publication