CN113831495A - 一种可控发泡时间的聚氨酯材料 - Google Patents
一种可控发泡时间的聚氨酯材料 Download PDFInfo
- Publication number
- CN113831495A CN113831495A CN202111041469.6A CN202111041469A CN113831495A CN 113831495 A CN113831495 A CN 113831495A CN 202111041469 A CN202111041469 A CN 202111041469A CN 113831495 A CN113831495 A CN 113831495A
- Authority
- CN
- China
- Prior art keywords
- parts
- polyurethane material
- reaction
- time
- catalyst
- 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 46
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 44
- 239000004814 polyurethane Substances 0.000 title claims abstract description 44
- 238000005187 foaming Methods 0.000 title claims abstract description 23
- 229920005862 polyol Polymers 0.000 claims abstract description 38
- 150000003077 polyols Chemical class 0.000 claims abstract description 38
- 239000012948 isocyanate Substances 0.000 claims abstract description 23
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 23
- 150000001412 amines Chemical class 0.000 claims abstract description 21
- 239000003054 catalyst Substances 0.000 claims abstract description 21
- 239000004088 foaming agent Substances 0.000 claims abstract description 21
- 239000000203 mixture Chemical class 0.000 claims abstract description 21
- 239000004970 Chain extender Substances 0.000 claims abstract description 14
- 229920003232 aliphatic polyester Polymers 0.000 claims abstract description 11
- 239000007809 chemical reaction catalyst Substances 0.000 claims abstract description 11
- 239000004094 surface-active agent Substances 0.000 claims abstract description 11
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 9
- 239000002202 Polyethylene glycol Substances 0.000 claims abstract description 6
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims abstract description 6
- 150000002009 diols Chemical class 0.000 claims abstract description 6
- 229920000515 polycarbonate Polymers 0.000 claims abstract description 6
- 239000004417 polycarbonate Substances 0.000 claims abstract description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims abstract description 6
- 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 claims abstract description 4
- KTRQTHPGQDBQNH-UHFFFAOYSA-N bis(cyclohexylmethyl) hexanedioate Chemical compound C1CCCCC1COC(=O)CCCCC(=O)OCC1CCCCC1 KTRQTHPGQDBQNH-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 34
- 238000003756 stirring Methods 0.000 claims description 16
- 239000011259 mixed solution Substances 0.000 claims description 11
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical group OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000000243 solution Substances 0.000 claims description 7
- 238000001816 cooling Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical group CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 claims description 4
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical compound [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 claims description 4
- 229910000020 calcium bicarbonate Inorganic materials 0.000 claims description 4
- 239000012975 dibutyltin dilaurate Substances 0.000 claims description 4
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical group [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims description 4
- 238000009740 moulding (composite fabrication) Methods 0.000 claims description 4
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims description 4
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 230000009471 action Effects 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000006260 foam Substances 0.000 abstract description 10
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract description 5
- 238000004080 punching Methods 0.000 abstract description 3
- 230000001934 delay Effects 0.000 abstract 1
- 241001669679 Eleotris Species 0.000 description 6
- 239000002994 raw material Substances 0.000 description 4
- 229920002396 Polyurea Polymers 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000006261 foam material Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229920006126 semicrystalline polymer Polymers 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/161—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
- C08G18/163—Catalysts 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
- C08G18/165—Catalysts 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/24—Catalysts containing metal compounds of tin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/44—Polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6603—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/6607—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6633—Compounds of group C08G18/42
- C08G18/6637—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
- C08G18/664—Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
-
- 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
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
- C08J9/08—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing carbon dioxide
-
- 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
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/02—CO2-releasing, e.g. NaHCO3 and citric acid
-
- 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
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/18—Binary blends of expanding agents
-
- 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
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/06—Polyurethanes from polyesters
-
- 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
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/08—Polyurethanes from polyethers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
本发明公开了一种可控发泡时间的聚氨酯材料,包括包括如下组分:多元醇组分30份、异氰酸酯组分40份、扩链剂5份、发泡剂10份、反应催化剂5份、表面活性剂5份和延时催化剂5份,多元醇组分选自饱和脂肪族聚酯多元醇、聚碳酸酯二醇、聚乙二醇与三羟甲基丙烷中的两种或多种,异氰酸酯组分选自1,4环己烷二甲醇己二酸酯与二苯基甲烷二异氰酸酯中的一种或多种,延时催化剂为封闭胺、热活化胺或热敏性胺与有机锡的混合物。本发明利用延时催化剂的设置,通过封闭胺、热活化胺或热敏性胺与有机锡的混合物制备成的延时催化剂,延迟发泡时间,使得整体混合物倒入模具后才开始发泡,进而能够实现完全冲模,提高了制备聚氨酯材料的质量。
Description
技术领域
本发明涉及聚氨酯材料制备领域,特别涉及一种可控发泡时间的聚氨酯材料。
背景技术
随着科技的发达,现在铁轨上的轨枕除了用木材或混凝土当原料,还有用聚氨酯材料来当原料进行使用的,聚氨酯材料质量轻、绝热性能优越,同时还具有良好的抗震性能,现在的聚氨酯材料都是通过多元醇和异氰酸酯作为原材料,进入催化剂、发泡剂和一些其他添加剂,通过半预聚体法或一步发泡法进行制备,但是现在在制备过程中,在发泡剂加入后,搅拌几秒后便开始发泡了,导致材料在没有倒入模具中便进行发泡,导致无法完全冲模,降低了制备出聚氨酯材料的质量。
发明内容
本发明的目的在于提供一种可控发泡时间的聚氨酯材料,以解决上述背景技术中提出的问题。
为实现上述目的,本发明提供如下技术方案:一种可控发泡时间的聚氨酯材料,包括如下组分:
优选的,所述多元醇组分选自饱和脂肪族聚酯多元醇、聚碳酸酯二醇、聚乙二醇与三羟甲基丙烷中的两种或多种。
优选的,所述异氰酸酯组分选自1,4环己烷二甲醇己二酸酯与二苯基甲烷二异氰酸酯中的一种或多种。
优选的,所述扩链剂为1,4丁二醇。
优选的,所述发泡剂为碳酸氢钙与水的混合物。
优选的,所述反应催发剂二丁基二月桂酸锡。
优选的,所述表面活性剂为十二烷基苯磺酸钠。
优选的,所述延时催化剂为封闭胺、热活化胺或热敏性胺与有机锡的混合物。
优选的,所述聚氨酯材料具有以下特性:
表观总密度:0.6-0.8g/cm3;
吸水量:<10mg/cm2;
弯曲弹性模量:>6GPa;
竖向压缩强度:>40MPa。
本发明还提供了一种一种可控发泡时间的聚氨酯材料的制备方法,包括如下步骤:
步骤一:将30份多元醇组分和40份异氰酸酯组分加入反应釜中,在反应釜内将温度加热至70℃后,对反应釜中的30份多元醇组分和40份异氰酸酯组分进行高速搅拌,搅拌完成后,向反应釜中多元醇组分和异氰酸酯组分的混合物中加入5份扩链剂和5份反应催发剂,再将反应釜中的反应温度调节至65℃,继续高速进行搅拌;
步骤二:搅拌完成后,再向30份多元醇组分、40份异氰酸酯组分、5份扩链剂和5份反应催发剂反应后的混合溶液中加入10份发泡剂、5份表面活性剂和5份延时催化剂,将反应釜内的温度设定为150℃,压力为10MPa,搅拌后直接将30份多元醇组分、40份异氰酸酯组分、5份扩链剂、5份反应催发剂、10份发泡剂、5份表面活性剂和5份延时催化剂的混合反应溶液直接导入模具中,在模具中冷却成型,同时因延时催发剂的作用,使得整体混合反应溶液在模具中冷却的同时并开始发泡,进而使得整体混合溶液可以完全在模具中进行冲模。
本发明的技术效果和优点:
(1)本发明利用延时催化剂的设置,通过封闭胺、热活化胺或热敏性胺与有机锡的混合物制备成的延时催化剂,延后发泡剂加入后在混合物的反应时间,同时减缓发泡剂在混合物的反应速度,使得整体混合物倒入模具后才开始发泡,进而能够实现完全冲模,提高了制备聚氨酯材料的质量;
(2)本发明利用脂肪族聚酯多元醇的设置,通过在多元醇组分中加入大量的脂肪族聚酯多元醇,使得制备出的聚氨酯材料表现出较大的强度,同时具有优良的耐磨性。
具体实施方式
下面将对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。
本发明提供了一种可控发泡时间的聚氨酯材料,包括如下组分:
多元醇组分选自饱和脂肪族聚酯多元醇、聚碳酸酯二醇、聚乙二醇与三羟甲基丙烷中的两种或多种,主要为饱和脂肪族聚酯多元醇与聚碳酸酯二醇的混合物、饱和脂肪族聚酯多元醇与聚乙二醇的混合物或者饱和脂肪族聚酯多元醇与三羟基丙烷的混合物,当使用饱和脂肪族聚酯多元醇与聚碳酸酯二醇、聚乙二醇或者三羟甲基丙烷混合时,饱和脂肪族聚酯多元醇占多元醇组分的60%朝上,最好为80%,可有效的保证所制备的聚氨酯材料的质量,使得聚氨酯材料强度更大,同时具有优良的耐磨性能,同时还可在多元醇组分中加入少量的己内酯系聚酯多元醇,其是半结晶性聚合物,官能度与起始剂精确匹配,数均分子量分布比较窄,具有良好的热稳定性,使得添加了己内酯系聚酯多元醇所制备出的聚氨酯材料具有较高的拉伸强度,同时具有一定的弹性,使得通过聚氨酯材料做出的轨枕在使用时可对轨枕受到的震动进行缓冲,有效的延长了聚氨酯材料做的轨枕的使用寿命,同时还具有良好的耐水性,因轨枕是露天放置,长时间受到雨水的淋湿,进而使得聚氨酯材料制作的轨枕更耐用;
异氰酸酯组分选自1,4环己烷二甲醇己二酸酯与二苯基甲烷二异氰酸酯中的一种或多种,通过异氰酸酯组分和多元醇组分现在反应釜内反应,形成预聚体,便于后续反应的进行;
扩链剂为1,4丁二醇,通过1,4丁二醇为原材料的扩链剂的使用,使得制备出的聚氨酯材料在力学性能方面更加优越;
发泡剂为碳酸氢钙与水的混合物,通过碳酸氢钙和水的混合物当做发泡剂,使得聚氨酯材料可有效的进行发泡,有效的增强制备出的聚氨酯材料的使用性能;
反应催发剂二丁基二月桂酸锡,二丁基二月桂酸锡为原料的反应催发剂可加快多元醇组分和异氰酸酯组分的反应时间,缩短了聚氨酯材料的制备的时间,提高了聚氨酯材料的制备效率;
表面活性剂为十二烷基苯磺酸钠,通过十二烷基苯磺酸钠为原料的表面活性剂使得混合溶液的表面张力显著下降,增加各组分的溶性,同时还起到乳化泡沫物料、稳定泡沫和调节泡孔的作用,同时还可加少量匀泡剂,在泡沫形成过程中,不溶性聚脲的析出会破坏泡沫的稳定,通过匀泡剂可使得聚脲分散,增大聚脲与泡沫基体的相容性,使得聚氨酯材料进行发泡时,其过程可更稳定,从而可进行均匀发泡;
延时催化剂为封闭胺、热活化胺或热敏性胺与有机锡的混合物,通过封闭胺、热活化胺或热敏性胺与有机锡的混合物作为延时催化剂,使得在发泡剂加入后,搅拌时不会立马使得发泡剂反应进行发泡,会使得发泡剂反应的时间延迟,进行再将混合溶液倒入模具后,混合溶液冷却的同时,发泡剂开始起作用,进而开始进行发泡,使得混合溶液在模具中可以完全冲模,从而使得制备的聚氨酯材料质量更好;
聚氨酯材料具有以下特性:表观总密度:0.6-0.8g/cm3;吸水量:<10mg/cm2;弯曲弹性模量:>6GPa;竖向压缩强度:>40MPa。
本发明工作原理:将30份多元醇组分和40份异氰酸酯组分加入反应釜中,在反应釜内将温度加热至70℃后,对反应釜中的30份多元醇组分和40份异氰酸酯组分进行高速搅拌,搅拌完成后,向反应釜中多元醇组分和异氰酸酯组分的混合物中加入5份扩链剂和5份反应催发剂,再将反应釜中的反应温度调节至65℃,继续高速进行搅拌,搅拌完成后,再向30份多元醇组分、40份异氰酸酯组分、5份扩链剂和5份反应催发剂反应后的混合溶液中加入10份发泡剂、5份表面活性剂和5份延时催化剂,将反应釜内的温度设定为150℃,压力为10MPa,搅拌后直接将30份多元醇组分、40份异氰酸酯组分、5份扩链剂、5份反应催发剂、10份发泡剂、5份表面活性剂和5份延时催化剂的混合反应溶液直接导入模具中,在模具中冷却成型,同时因延时催发剂的作用,使得整体混合反应溶液在模具中冷却的同时并开始发泡,进而使得整体混合溶液可以完全在模具中进行冲模,使得制备出的聚氨酯材料质量更好。
最后应说明的是:以上所述仅为本发明的优选实施例而已,并不用于限制本发明,尽管参照前述实施例对本发明进行了详细的说明,对于本领域的技术人员来说,其依然可以对前述各实施例所记载的技术方案进行修改,或者对其中部分技术特征进行等同替换,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (10)
2.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述多元醇组分选自饱和脂肪族聚酯多元醇、聚碳酸酯二醇、聚乙二醇与三羟甲基丙烷中的两种或多种。
3.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述异氰酸酯组分选自1,4环己烷二甲醇己二酸酯与二苯基甲烷二异氰酸酯中的一种或多种。
4.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述扩链剂为1,4丁二醇。
5.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述发泡剂为碳酸氢钙与水的混合物。
6.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述反应催发剂二丁基二月桂酸锡。
7.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述表面活性剂为十二烷基苯磺酸钠。
8.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述延时催化剂为封闭胺、热活化胺或热敏性胺与有机锡的混合物。
9.根据权利要求1所述的一种可控发泡时间的聚氨酯材料,其特征在于,所述聚氨酯材料具有以下特性:
表观总密度:0.6-0.8g/cm3;
吸水量:<10mg/cm2;
弯曲弹性模量:>6GPa;
竖向压缩强度:>40MPa。
10.一种可控发泡时间的聚氨酯材料的制备方法,包括如下步骤:
步骤一:将30份多元醇组分和40份异氰酸酯组分加入反应釜中,在反应釜内将温度加热至70℃后,对反应釜中的30份多元醇组分和40份异氰酸酯组分进行搅拌,搅拌完成后,向反应釜中多元醇组分和异氰酸酯组分的混合物中加入5份扩链剂和5份反应催发剂,再将反应釜中的反应温度调节至65℃,继续进行搅拌;
步骤二:搅拌完成后,再向30份多元醇组分、40份异氰酸酯组分、5份扩链剂和5份反应催发剂反应后的混合溶液中加入10份发泡剂、5份表面活性剂和5份延时催化剂,将反应釜内的温度设定为150℃,压力为10MPa,搅拌后直接将30份多元醇组分、40份异氰酸酯组分、5份扩链剂、5份反应催发剂、10份发泡剂、5份表面活性剂和5份延时催化剂的混合反应溶液直接导入模具中,在模具中冷却成型,同时因延时催发剂的作用,使得整体混合反应溶液在模具中冷却的同时并开始发泡,进而使得整体混合溶液可以完全在模具中进行冲模。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111041469.6A CN113831495A (zh) | 2021-09-07 | 2021-09-07 | 一种可控发泡时间的聚氨酯材料 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111041469.6A CN113831495A (zh) | 2021-09-07 | 2021-09-07 | 一种可控发泡时间的聚氨酯材料 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN113831495A true CN113831495A (zh) | 2021-12-24 |
Family
ID=78962423
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202111041469.6A Pending CN113831495A (zh) | 2021-09-07 | 2021-09-07 | 一种可控发泡时间的聚氨酯材料 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113831495A (zh) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR820001053B1 (ko) * | 1978-05-10 | 1982-06-12 | 윌리암 에취. 브류스터 | 경질 폴리우레탄 폼의 제조방법 |
US5300532A (en) * | 1991-04-25 | 1994-04-05 | Toyoda Gosei Co., Ltd. | Integral skin-foam molded article |
CN101597370A (zh) * | 2008-06-06 | 2009-12-09 | 上海合达聚合物科技有限公司 | 一种水发泡自结皮聚氨酯组合物、其制备方法及应用 |
CN103113865A (zh) * | 2013-03-07 | 2013-05-22 | 中国矿业大学 | 矿用延缓发泡型聚合物封孔材料 |
CN108892769A (zh) * | 2018-06-19 | 2018-11-27 | 石家庄合汇化工有限公司 | 一种用于制备聚氨酯的酸封延迟性催化剂 |
CN110437418A (zh) * | 2019-08-29 | 2019-11-12 | 万华化学集团股份有限公司 | 一种延迟发泡的硬质聚氨酯泡沫及其制备方法 |
-
2021
- 2021-09-07 CN CN202111041469.6A patent/CN113831495A/zh active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR820001053B1 (ko) * | 1978-05-10 | 1982-06-12 | 윌리암 에취. 브류스터 | 경질 폴리우레탄 폼의 제조방법 |
US5300532A (en) * | 1991-04-25 | 1994-04-05 | Toyoda Gosei Co., Ltd. | Integral skin-foam molded article |
CN101597370A (zh) * | 2008-06-06 | 2009-12-09 | 上海合达聚合物科技有限公司 | 一种水发泡自结皮聚氨酯组合物、其制备方法及应用 |
CN103113865A (zh) * | 2013-03-07 | 2013-05-22 | 中国矿业大学 | 矿用延缓发泡型聚合物封孔材料 |
CN108892769A (zh) * | 2018-06-19 | 2018-11-27 | 石家庄合汇化工有限公司 | 一种用于制备聚氨酯的酸封延迟性催化剂 |
CN110437418A (zh) * | 2019-08-29 | 2019-11-12 | 万华化学集团股份有限公司 | 一种延迟发泡的硬质聚氨酯泡沫及其制备方法 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107602817B (zh) | 一种高耐寒聚氨酯减震垫及其制备方法 | |
CN109912768B (zh) | 一种聚醚组合物、低voc聚氨酯泡沫及其制备方法 | |
CN104403079B (zh) | 一种快速修复沥青路面裂缝的聚合物材料及其制备方法 | |
CZ188995A3 (en) | Foamy polymer and process for preparing thereof | |
CN100569823C (zh) | 一种聚醚型聚氨酯鞋底及其制备方法 | |
CN101565495A (zh) | 聚氨酯弹性体及其制备方法和用途 | |
CN101486834A (zh) | 一种高性能纳米聚氨酯微孔弹性体复合材料及其制备方法 | |
CN101215391B (zh) | 一种氯化聚乙烯改性丁腈橡胶发泡材料的制备方法 | |
CN104558496A (zh) | 一种热塑性聚氨酯微孔弹性体及其制备方法 | |
CN101987883B (zh) | 低密度全mdi基高回弹聚氨酯泡沫塑料的制备及应用 | |
WO2022134296A1 (zh) | 一种高回弹生物可降解聚酯微发泡异型材的制备方法 | |
CN110951045A (zh) | 用于吸湿性鞋垫的聚氨酯弹性体组合物及其制备方法 | |
CN110903627A (zh) | 一种热塑性弹性体共混物超临界发泡材料及其制备方法 | |
CN108440783A (zh) | 一种聚氨酯发泡珠粒及其制备方法 | |
CN111234492A (zh) | 一种pla/tpu超临界发泡复合材料及其制备方法 | |
CN113831495A (zh) | 一种可控发泡时间的聚氨酯材料 | |
CN107614615A (zh) | 引入可供交联位臵的热塑性聚氨酯及采用其进行交联发泡的方法 | |
US3277026A (en) | Method of making resilient cellular rubber material containing expanded polystyrene granules therein | |
CN113308019A (zh) | 一种开孔剂及其制备方法和应用 | |
CN111909341B (zh) | 一种聚氨酯的制备方法 | |
US2888413A (en) | Preparation of flexible elastomeric cellular polyurethane materials | |
CN116461035A (zh) | 一种超临界发泡材料的制备工艺及超临界发泡材料 | |
CN112708093B (zh) | 板材用聚氨酯原料组合物、聚氨酯保温材料及其制备方法 | |
CN105524251A (zh) | 一种具有高回弹性的海绵及其制备工艺 | |
CN113861489A (zh) | 一种聚氨酯发泡的泡沫冷拌沥青混合料及其制备方法 |
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 | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20211224 |