CN113845640A - Polyether polyol for polyurethane foam plastic and preparation method and application thereof - Google Patents
Polyether polyol for polyurethane foam plastic and preparation method and application thereof Download PDFInfo
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- CN113845640A CN113845640A CN202111351663.4A CN202111351663A CN113845640A CN 113845640 A CN113845640 A CN 113845640A CN 202111351663 A CN202111351663 A CN 202111351663A CN 113845640 A CN113845640 A CN 113845640A
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- polyether polyol
- polyurethane foam
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- 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
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5075—Polyethers having heteroatoms other than oxygen having phosphorus
- C08G18/5081—Polyethers having heteroatoms other than oxygen having phosphorus having phosphorus bound to oxygen only
- C08G18/5084—Phosphate compounds
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- 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
- C08G2101/00—Manufacture of cellular products
Abstract
The polyurethane foam plastic prepared based on the polyether polyol has the advantages of high compression strength, good dimensional stability, less moisture absorption and swelling problems in rainy days, excellent solvent resistance and flame retardance, and can well meet the application requirements of polyurethane spraying. The preparation method of the polyether polyol for the polyurethane foam provided by the invention comprises the following steps: s1, carrying out phosphorylation modification on polyether polyol by polyphosphoric acid to generate polyether polyol phosphate, wherein the polyether polyol phosphate contains partial hydroxyl; and S2, epoxidizing and modifying the polyether polyol phosphate obtained in the step S1 by using epoxy resin to generate the polyether polyol for the polyurethane foam, wherein the molecular structure of the epoxy resin contains benzene rings.
Description
Technical Field
The invention relates to modified polyether polyol, in particular to polyether polyol for polyurethane foam plastic and a preparation method and application thereof.
Background
Polyurethane is a high molecular material containing repeated structural units of carbamate, can be prepared into products with various shapes, such as foamed plastics, elastomers, adhesives, synthetic leather coating resins and the like, and has wide application in the fields of clothing and eating, housing, industrial and agricultural production, building, traffic, medical treatment and the like. The polyurethane material has various performance advantages, such as a layer of polyurethane rigid foam sprayed on the surface of the inner wall of the refrigeration house, and has the advantages of heat preservation, heat insulation, water resistance and energy conservation. However, the common polyurethane foam plastic has the defects of poor mechanical property, poor dimensional stability, easy moisture absorption, poor solvent resistance, poor flame retardance and the like, is very easy to deform under pressure under the action of external force, and is easy to shrink in size even without the action of external force; when the weather is rainy, the phenomenon of moisture absorption and bulging can occur, and the application range of the water-absorbing paint is greatly limited. CN1515602A discloses an asphalt polyurethane rigid foam, which adopts potassium alkoxide composite catalyst to improve the dimensional stability of the rigid foam, but because the dosage of the catalyst in the system is very small, the two main raw materials of polyether and isocyanate are not changed, so that the improvement effect of the dimensional stability is very limited.
The cured epoxy resin has the advantages of high mechanical strength, good dimensional stability, strong hydrophobicity, good heat resistance, safety, environmental protection and the like, and can improve the application performance of the polyurethane foam plastic by utilizing the epoxy resin. CN102924692A adopts epoxy resin blended modified polyurethane to prepare an epoxy resin-polyurethane interpenetrating network material, but because of different solubilities of epoxy resin and polyurethane, two phases in the system are separated to a certain degree, and the performance improvement effect is greatly reduced. CN111269647A adopts epoxy resin to carry out chemical modification on the polyurethane coating so as to enhance the wear resistance, moisture permeability and oxidation resistance of the polyurethane coating, but the chemical modification principle is very fuzzy, and the change situation of the properties such as mechanical strength of the modified coating is not discussed.
In order to solve the problems, the industry needs to develop a novel polyurethane foam plastic which has good mechanical property and dimensional stability and is difficult to absorb moisture so as to expand the application of the polyurethane foam plastic in the fields of cold storage spraying, pipeline heat preservation, plate filling, household appliance heat insulation and the like.
Disclosure of Invention
In view of the above, the invention provides polyether polyol for polyurethane foam plastic and a preparation method and application thereof, polyether polyol for polyurethane foam plastic is obtained by reacting polyether polyol with epoxy resin after the polyether polyol is subjected to phosphorylation modification, and polyurethane foam plastic prepared based on the polyether polyol for polyurethane foam plastic has the advantages of high compression strength, good dimensional stability, less problems of moisture absorption and swelling in rainy days, excellent solvent resistance and flame retardance, and capability of well meeting the application requirements of polyurethane spraying.
In order to achieve the purpose, the technical scheme adopted by the invention is as follows:
the invention provides a preparation method of polyether polyol for polyurethane foam, which comprises the following steps:
s1, carrying out phosphorylation modification on polyether polyol by polyphosphoric acid to generate polyether polyol phosphate, wherein the polyether polyol phosphate contains partial hydroxyl;
and S2, epoxidizing and modifying the polyether polyol phosphate obtained in the step S1 by using epoxy resin to generate the polyether polyol for the polyurethane foam, wherein the molecular structure of the epoxy resin contains benzene rings.
Further, the polyether polyol in step S1 has the following chemical formula (II):
wherein R is1Is alkyl or hydrogen, n is the polymerization degree of polyether polyol, x is the functionality of an initiator used for preparing the polyether polyol shown in the formula (II), x is more than or equal to 3, and Y is a structure of the initiator after active hydrogen is removed; the initiator may be those commonly used in the art for preparing polyether polyols, such as polyols, polyamines, or other active hydrogen-containing compounds, as exemplified by xylitol as the initiatorY is then
The polyether polyol for the polyurethane foam provided by the invention has hydroxyl, and epoxy groups, benzene rings and phosphorus elements are introduced into molecules, so that when the polyether polyol is used as one of main raw materials of the polyurethane foam, the mechanical property, the dimensional stability and the solvent resistance of the foam can be effectively improved, the moisture absorption and swelling phenomenon of spraying the foam can be improved, and the flame retardant property can be obviously improved. In some embodiments, the polyether polyols for polyurethane foams of the present invention may be represented by the following structural formula (I):
in the formula (I), Y, R1N, x have the same meanings as described above with respect to formula (II), and are not described in detail. q is the number of hydroxyl groups participating in the phosphorylation reaction, and q is less than x; r2Is Ep; r3Is Ep or hydrogen; wherein Ep is a structure of an epoxy group of an epoxy resin molecule after ring opening, the epoxy resin molecule contains a benzene ring, and for example, bisphenol A diglycidyl ether type epoxy resin molecules are as follows:
wherein Ep formed after ring opening of one epoxy group is:
and m is the polymerization degree of the epoxy resin.
In some embodiments, the polyether polyol phosphate obtained in step S1 may be represented by the following structural formula (III):
in terms of reaction kinetics, it is not controllable that a part of or all of the hydroxyl groups on the polyether polyol (represented by formula (II)) in step S1 participate in the phosphorylation reaction. The invention solves the problem by controlling the feeding amount of polyphosphoric acid, and the prepared polyether polyol phosphate not only contains phosphate ester groups, but also reserves partial hydroxyl (shown as a formula III). Preferably, in step S1, the ratio of the phosphorus atoms in the polyphosphoric acid to the hydroxyl groups in the polyether polyol (formula (II)) is controlled to be 1 (1.8-2.2). When the feeding ratio is higher than 1:1.8, phosphorus atoms are relatively excessive, the hydroxyl groups of the reacted polyether polyol are less, and the reactivity and the mechanical strength are obviously reduced when the polyether polyol is used for polyurethane foaming; when the feeding ratio is lower than 1:2.2, the polyphosphoric acid is relatively less, the reaction degree is reduced, and the effect of the epoxy resin modified polyether polyol is reduced.
Preferably, in step S1, the polyphosphoric acid is diluted with a solvent before feeding, and added dropwise to the reaction system after dilution; preferably, the mass ratio of the polyphosphoric acid to the solvent is 1: (0.8 to 1.2). The present inventors have surprisingly found through studies that it is not feasible to react pure polyphosphoric acid with a polyfunctional polyether polyol and that the reaction mass changes from colorless to dark brown to black in a short time, because the dehydration properties of polyphosphoric acid are close to those of concentrated sulfuric acid, resulting in slight charring of the reaction mass. The invention reduces the dehydration property of polyphosphoric acid by diluting the polyphosphoric acid with a solvent, effectively solves the problem and enables the reaction to be carried out stably. Preferably, the solvent is selected from one or more of ethanol, dichloromethane, chloroform, dimethyl carbonate, methyl acetate and ethyl acetate. More preferably ethanol is the solvent. The method adopts a dropwise adding mode to add the polyphosphoric acid solution into the polyether polyol, can ensure the stable reaction, and avoids dehydration and carbonization of reactants caused by over violent reaction and over quick heat release.
In some embodiments, in step S1, the temperature of the reaction system is preheated to 50 to 60 ℃ in advance, and after the temperature of the reaction system is stable (for example, the temperature fluctuation range is within ± 1 ℃), the temperature is raised to 75 to 85 ℃ to react for 2 to 6 hours; preferably, the temperature rise is performed in a slow temperature rise manner, for example, the temperature rise rate of the temperature rise is 3 ℃/min.
In some embodiments, the post-processing operation after the end of the reaction in step S1 includes: extracting the resulting product with ethyl acetate and retaining the organic phase, then washing the organic phase with deionized water, repeating the extraction, the washing operation a plurality of times (e.g., 3 times) until the aqueous phase is added dropwise to the CaCl2No precipitate is separated out from the saturated aqueous solution; then dried (e.g. with anhydrous Na)2SO4Drying) the organic phase, filtering, and removing the solvent (e.g., by rotary evaporation) to obtain the target product, polyether polyol phosphate; the amount of the extractant ethyl acetate used is not particularly limited, so that the aqueous phase is finally added dropwise to the CaCl2No precipitate is precipitated in the saturated aqueous solution.
Preferably, in step S2, the epoxy resin is one or more of glycidyl ether epoxy resin, glycidyl ester epoxy resin, glycidyl amine epoxy resin, and alicyclic epoxy resin, each of which has a molecular structure containing a benzene ring.
Preferably, the charging ratio of the phosphorus atom of the target product obtained in the step S1 to the epoxy resin molecule in the step S2 is 1 (1.0-1.3); by adopting the molar ratio, more epoxy resin molecules can be grafted to the phosphate ester groups, and the product contains the hydroxyl groups of the polyol and the epoxy groups.
Preferably, the reaction of step S2 is carried out at room temperature for a reaction time of 0.5 to 1 hour. The room temperature is changed according to different environments, and in the invention, the room temperature can be 10-30 ℃. The target product obtained in step S2 requires no post-processing.
The invention also provides polyether polyol for polyurethane foam, which is prepared by the method.
The present invention also provides a polyurethane foam prepared using a composition comprising an isocyanate and the above-mentioned polyether polyol for polyurethane foam;
preferably, the components comprise A, B, C components, wherein the total mass of the A component and the B component is 100 percent:
the component A comprises:
and B component:
2 to 3.5 weight percent of catalyst,
7-17 wt% of curing agent;
the component C is isocyanate, and the ratio of the total mass of the component A and the component B to the mass of the component C is 1: (1 to 1.7).
Wherein, the foam stabilizer is preferably one or more of Jiangsu Maiside chemical M-8809, M-8803, M-8806, Ma chart L6900 and Yingchuang B8545, preferably one or more of M-8809, M-8803 and M-8806;
preferably, the foaming agent is one or more of chlorofluorocarbon, alkane or hydrofluorocarbon foaming agents, preferably hydrofluorocarbon foaming agents, more preferably one or two of HONEYWELL HFC-245fa and HFC-365 mfc;
preferably, the catalyst is a tertiary amine or organotin catalyst, preferably N, N-dimethylcyclohexylamine, organotin or a complex catalyst, more preferably warfarinPMDETA, New classical chemical T-12,One or more of SPs 703.
Preferably, the curing agent is one or more of 4, 4-diaminodicyclohexyl methane, 3-aminomethyl-3, 5, 5-trimethyl cyclohexylamine or polyether amine, preferably Wanhua2110、PACM、IPDA or8100.
Preferably, the isocyanate is a polymeric isocyanate, preferably a polymethylene polyphenyl isocyanate, more preferably WanhuaPM-200、One or two of PM-400.
In some embodiments, the polyurethane foam is prepared before application by a A, B, C three-component mixing method, which comprises the following steps:
(1) respectively and uniformly mixing the A, B components at 10-40 ℃, and respectively discharging, sealing and storing;
(2) at the temperature of 10-40 ℃, respectively mixing A, B components and C components according to the mass ratio (A + B): c is 1: (1-1.7) mixing uniformly, and then using.
The invention also provides application of the polyurethane foam plastics, and the polyurethane foam plastics are applied to the fields of cold storage spraying, pipeline heat preservation, plate filling and household appliance heat insulation (such as refrigerator heat insulation). In some embodiments, the specific application method is as follows: when the coating is applied to spraying of a cold storage, A, B are respectively and uniformly mixed by a spraying machine, A, B, C is uniformly mixed and directly sprayed on the wall surface of the cold storage, and foaming and curing are carried out at the temperature of 10-40 ℃; when the A, B, C three-component composite is applied to pipeline heat preservation, the A, B, C three-component composite which is evenly mixed is extruded, injected or sprayed and wound on the surface of a pipeline, and is foamed and cured at the temperature of 10-30 ℃; when the A, B, C three-component mixture is applied to filling of the plate, the A, B, C three-component mixture is coated on the surface of the plate, and foaming, forming, curing and demoulding are carried out at the temperature of 10-30 ℃; when the polyurethane foam is applied to heat preservation of a refrigerator, A, B, C three groups which are uniformly mixed are injected into a mould for foaming, molding and curing, and the required polyurethane foam is obtained.
The polyurethane foam plastic prepared from the polyether polyol for polyurethane foam plastic has high compression strength, low dimensional change rate, excellent hydrophobicity, solvent resistance and flame retardance under the room temperature condition, and meets the requirements of the polyurethane foam plastic industry. For example, some embodiments achieve a compressive strength of 0.52MPa (0.12 MPa, Calif.) and a dimensional change of less than 0.8% (70 ℃, 4% Calif.) and 0.3% (20 ℃, 1% Calif.).
The invention adopts a chemical modification mode to introduce the epoxy resin with a benzene ring structure into the field of polyurethane foam plastics. When the polyether polyol is subjected to phosphorylation modification, the polyphosphoric acid is diluted by a solvent and then reacts with the polyether polyol in a dropwise manner, so that dehydration and carbonization of reactants caused by over violent reaction and over quick heat release are effectively avoided; the phosphoric acid esterification is used as a bridge for introducing epoxy resin into polyether polyol, and partial epoxidation of the polyether polyol is realized by reasonably controlling the feeding amount of polyphosphoric acid and the epoxy resin, so that a target product has the performances of phosphate and the epoxy resin; compared with the common polyether polyol, the epoxy resin molecular chain segment containing benzene rings is introduced into the prepared polyurethane foam plastic, the mechanical property and the size stability are obviously improved, the compression deformation during the action of external force and the size shrinkage during the absence of external force are effectively reduced, the problem that the polyurethane foam is easy to absorb moisture and swell in rainy days is solved, meanwhile, the solvent resistance and the flame retardant property of the foam plastic are further improved due to the introduction of the benzene rings and the phosphorus elements, and the application range of the polyurethane foam plastic is greatly expanded.
The technical scheme provided by the invention has the following beneficial effects:
(1) the invention adopts a chemical modification method to introduce the epoxy resin into polyether polyol molecules, applies the scheme to the field of polyurethane foam plastics for the first time, has wide sources of raw materials of the epoxy resin and the polyether polyol, has simple preparation process conditions and high production efficiency, and is easy to realize industrialization. In the prior art, an epoxy compound with a benzene ring is introduced when polyether polyol is synthesized by using an initiator directly at the upstream, the process needs to involve the use of a catalyst, a polymerization inhibitor and a blocking agent, and strict temperature control and strict catalyst dosage control are needed to prepare epoxy modified polyether polyol with specific molecular weight, so that the process requirement is strict; compared with the prior art, the invention has relatively loose process conditions, does not relate to the use of the reagent, and is easy to implement and control.
(2) When the modified polyether polyol is prepared, epoxy resin molecules containing a benzene ring structure are adopted for modification, and the polyether polyol prepared by the method is used as a raw material for polyurethane spraying, so that the prepared polyurethane foam plastic is high in compression strength and good in size stability, and can effectively resist size shrinkage in a long-term use process and compression deformation under the action of external force; the solvent resistance of the foam is further improved.
(3) Meanwhile, the hydrophobic property of the polyether polyol is greatly improved by introducing the epoxy resin into the polyether polyol molecular chain segment, and the problem of moisture absorption and swelling of the foam plastic can be obviously improved in the polyurethane spraying construction process.
(4) In addition, the polyether polyol prepared by the method is rich in phosphorus elements, and the polyether polyol is used as a main raw material of polyurethane foam, so that the overall flame retardant property of the plastic is obviously improved.
(5) In terms of reaction kinetics, part of or all of the hydroxyl groups of the polyether polyol participate in the phosphorylation reaction, which is an uncontrollable process. According to the invention, by controlling the feeding amount of polyphosphoric acid, the novel polyether polyol molecule containing epoxy groups and phosphoric ester bonds and retaining part of hydroxyl groups is synthesized, so that the novel polyurethane foam plastic with the performance advantages is prepared, the industry development trend is met, and the market prospect is wide.
Detailed Description
In order to better understand the technical solution of the present invention, the following examples are further provided to illustrate the present invention, but the present invention is not limited to the following examples.
Information of the used main raw materials:
polyphosphoric acid: shanghai Aladdin Biotechnology GmbH;
wherein R is1Is methyl, n is 1, x is 4, Y is
Glycidyl ether type epoxy resin: WSR618, synthetic materials ltd, star, south star, star;
glycidyl amine type epoxy resin: syna Epoxy S-720, New Nantong Xinnaxi Material Co., Ltd;
glycidyl ether type epoxy resin: WSR6101, blue star southwestern stars synthetic materials ltd;
foam stabilizer: m-8809, M-8806, Maxwell chemical Co., Ltd;
foaming agent: HFC-245fa, Honeywell;
catalyst: t-12, New classical chemical materials (Shanghai) Co., Ltd;
the test method comprises the following steps:
compressive strength: refer to GB/T8813-;
dimensional stability: refer to GB/T8811-;
water absorption: refer to GB/T8810 & 2005 rigid foam Water absorption determination;
solvent resistance: preparing polyurethane foam into small blocks with the specification of 15mm multiplied by 15mm, putting the small blocks into an oven to be completely dried and weighed, then soaking the small blocks for 14 days at room temperature by using 10 wt% of hydrochloric acid, 10 wt% of acetic acid and 10 wt% of ethanol aqueous solution, airing the surfaces, weighing again, and calculating the solvent-resistant swelling ratio eta according to the following formula:
η=(m-m0)/m0×100%
in the formula, m represents the mass of a sample block after being soaked for 14 days, and g represents the mass of the sample block;
m0-mass of sample block before soaking, g;
flame retardant property: the combustion behavior was determined by the oxygen index method with reference to GB/T2406.2-2009, part 2: room temperature test ";
hydroxyl value: refer to GB 12008.3-1989 method for determining hydroxyl value in polyether polyol.
[ example 1 ]
Polyether polyol # 1 for polyurethane foam was prepared as follows:
169g of polyphosphoric acid is dissolved in 169g of absolute ethanol to prepare an absolute ethanol solution of polyphosphoric acid, and then the solution is dropwise added to 300g of polyether polyol in 3 batchesIn R2403 (ensuring the molar ratio of phosphorus atoms of polyphosphoric acid to hydroxyl groups in the polyether polyol raw material to be 1:2), preheating the temperature of a reaction system to 50-60 ℃, and raising the temperature to 80 ℃ for reaction for 4 hours when the temperature of the system is stabilized at 55 ℃. Extracting the product with ethyl acetate (volume ratio of extractant to extracted liquid is 1:1), retaining organic phase, washing organic phase with deionized water, extracting, washing for 3 times, and adding water phase into CaCl2No precipitate is separated out from the saturated solution, and anhydrous Na is used2SO4Drying the organic phase, filtering, and removing the solvent by rotary evaporation to obtain the target product polyether polyol phosphate (the hydroxyl value of the polyether polyol is reduced from 760mgKOH/g to 382mgKOH/g before and after the reaction).
460g of polyether polyol phosphate and 748g of glycidyl ether type epoxy resin WSR618 (the molar ratio of phosphorus atoms to epoxy resin molecules is 1:1.1) are stirred and reacted for 45min at room temperature, and the target product polyether polyol for polyurethane foam is obtained, and the product does not need to be subjected to post-treatment.
[ example 2 ]
Polyether polyol # 2 for polyurethane foam was prepared as follows:
169g of polyphosphoric acid was dissolved in 135g of dichloromethane to prepare an absolute ethanol solution of polyphosphoric acid, which was then added dropwise to 270g of polyether polyol in 3 batchesIn R2403 (ensuring the molar ratio of phosphorus atoms of polyphosphoric acid to hydroxyl groups in the polyether polyol raw material to be 1:1.8), preheating the temperature of a reaction system to 50-60 ℃, and heating to 75 ℃ after the temperature of the system is stabilized at 50 ℃ for reacting for 6 hours. Extracting the product with ethyl acetate (volume ratio of extractant to extracted liquid is 1:1), retaining organic phase, washing organic phase with deionized water, extracting, washing for 3 times, and adding water phase into CaCl2No precipitate is separated out from the saturated solution, and anhydrous Na is used2SO4Drying the organic phase, filtering, and removing the solvent by rotary evaporation to obtain the target product polyether polyol phosphate (the hydroxyl value of the polyether polyol before and after the reaction is reduced from 760mgKOH/g to 353 mgKOH/g).
460g of polyether polyol phosphate and 845g of glycidyl amine type Epoxy resin Syna Epoxy S-720 (the molar ratio of phosphorus atoms to Epoxy resin molecules is 1:1) are stirred and reacted for 60min at room temperature, and the target product polyether polyol for polyurethane foam is obtained, and the product does not need post-treatment.
[ example 3 ]
Polyether polyol # 3 for polyurethane foam was prepared as follows:
169g of polyphosphoric acid was dissolved in 152g of dimethyl carbonate to prepare an absolute ethanol solution of polyphosphoric acid, which was then added dropwise to 330g of polyether polyol in 3 batchesIn R2403 (ensuring the molar ratio of phosphorus atoms of polyphosphoric acid to hydroxyl groups in the polyether polyol raw material to be 1:2.2), preheating the temperature of a reaction system to 50-60 ℃, and raising the temperature to 85 ℃ for reaction for 2 hours when the temperature of the system is stabilized at 60 ℃. Extracting the product with ethyl acetate (volume ratio of extractant to extracted liquid is 1:1), retaining organic phase, washing organic phase with deionized water, extracting, washing for 3 times, and adding water phase into CaCl2No precipitate is separated out from the saturated solution, and anhydrous Na is used2SO4Drying the organic phase, filtering, and removing the solvent by rotary evaporation to obtain the target product polyether polyol phosphate (the hydroxyl value of the polyether polyol before and after the reaction is reduced from 760mgKOH/g to 416 mgKOH/g).
460g of polyether polyol phosphate and 1091g of epoxy resin WSR6101 (the molar ratio of phosphorus atoms to epoxy resin molecules is 1:1.2) are stirred and reacted for 30min at room temperature, so that the target product polyether polyol for polyurethane foam is obtained, and the product does not need post-treatment.
[ example 4 ]
Polyether polyol # 4 for polyurethane foam was prepared as follows:
169g of polyphosphoric acid are dissolved in 186g of methyl acetate to prepare an absolute ethanol solution of polyphosphoric acid, and then the solution is dropwise added to 285g of polyether polyol in 3 batchesIn R2403 (ensuring the molar ratio of phosphorus atoms of polyphosphoric acid to hydroxyl groups in the polyether polyol raw material to be 1:1.9), preheating the temperature of a reaction system to 50-60 ℃, and raising the temperature to 78 ℃ after the temperature of the system is stabilized at 53 ℃ for reacting for 3 hours. Extracting the product with ethyl acetate (volume ratio of extractant to extracted liquid is 1:1), retaining organic phase, washing organic phase with deionized water, extracting, washing for 3 times, and adding water phase into CaCl2No precipitate is separated out from the saturated solution, and anhydrous Na is used2SO4Drying the organic phase, filtering, and removing the solvent by rotary evaporation to obtain the target product polyether polyol phosphate (the hydroxyl value of the polyether polyol before and after the reaction is reduced from 760mgKOH/g to 361 mgKOH/g).
460g of polyether polyol phosphate and 885g of epoxy resin WSR618 (the molar ratio of phosphorus atoms to epoxy resin molecules is 1:1.3) are stirred and reacted for 40min at room temperature, and the target product polyether polyol for polyurethane foam is obtained, and the product does not need post-treatment.
[ example 5 ]
Polyether polyol # 5 for polyurethane foam was prepared as follows:
169g of polyphosphoric acid was dissolved in 203g of ethyl acetate to prepare an absolute ethanol solution of polyphosphoric acid, which was then added dropwise to 315g of polyether polyol in 3 batchesIn R2403 (ensuring the molar ratio of phosphorus atoms to hydroxyl groups to be 1:2.1), preheating the temperature of a reaction system to between 50 and 60 ℃, and raising the temperature to 83 ℃ after the temperature of the system is stabilized at 58 ℃ for reaction for 5 hours. Extracting the product with ethyl acetate (volume ratio of extractant to extracted liquid is 1:1), retaining organic phase, washing organic phase with deionized water, extracting, washing for 3 times, and adding water phase into CaCl2No precipitate is separated out from the saturated solution, and anhydrous Na is used2SO4Drying the organic phase, filtering, and removing the solvent by rotary evaporation to obtain the target product polyether polyol phosphate (the hydroxyl value of the polyether polyol before and after the reaction is reduced from 760mgKOH/g to 402 mgKOH/g).
460g of polyether polyol phosphate and 930g of Epoxy resin Syna Epoxy S-720 (the molar ratio of phosphorus atoms to Epoxy resin molecules is 1:1.1) are stirred and reacted for 50min at room temperature, and the target product polyether polyol for polyurethane foam is obtained, and the product does not need post-treatment.
[ example 6 ]
Polyurethane foams were prepared as follows:
separately, A, B, C components were prepared:
the component A comprises: 630g of polyether polyol 1# for polyurethane foam, 15g of foam stabilizer M-8809, 250g of foaming agent HFC-245fa and 15g of water are fully and uniformly mixed.
And B component: 10g of catalystPMDETA, 10g catalystSP703, 40g curing agent2110, 30g curing agentIPDA (Wanhua chemical) was mixed well.
Respectively and uniformly mixing A, B at 25 ℃ by using a spraying machine, and mixing A, B, C according to the mass ratio (A + B): c is 1:1.3, mixing evenly and spraying the mixture on the wall surface of a cold storage, foaming and curing at 25 ℃ to obtain the polyurethane foam plastics, wherein the performance test results are shown in tables 1 and 2.
[ example 7 ]
Polyurethane foams were prepared as follows:
separately, A, B, C components were prepared:
the component A comprises: 580g of polyether polyol 2# for polyurethane foam, 20g of foam stabilizer M-8803, 240g of foaming agent HFC-365mfc and 13g of water are fully and uniformly mixed.
And B component: 14g of catalystPMDETA, 13g catalystSP703, 60g curing agent2110, 60g curing agent8110 mixing well.
Respectively and uniformly mixing A, B at 25 ℃ by using a spraying machine, and mixing A, B, C according to the mass ratio (A + B): c is 1:1, uniformly mixing and directly spraying the mixture on the wall surface of a cold storage, foaming and curing at 25 ℃ to obtain the polyurethane foam plastics, wherein the performance test results are shown in tables 1 and 2.
[ example 8 ]
Polyurethane foams were prepared as follows:
separately, A, B, C components were prepared:
the component A comprises: 680g of polyurethane foam plastic polyether polyol No. 3, 10g of foam stabilizer M-8806, 200g of foaming agent cyclopentane and 6g of water are mixed evenly.
And B component: 19g of catalystPMDETA, 15g of catalyst T-12, 40g of curing agentPACM, 30g curing agent8100 mixing well.
Respectively and uniformly mixing A, B at 25 ℃ by using a spraying machine, and mixing A, B, C according to the mass ratio (A + B): c is 1: 1.7, mixing uniformly and spraying the mixture on the wall surface of a cold storage directly, foaming and curing at 25 ℃ to obtain the polyurethane foam plastics, wherein the performance test results are shown in tables 1 and 2.
[ example 9 ]
Polyurethane foams were prepared as follows:
separately, A, B, C components were prepared:
the component A comprises: 580g of polyether polyol 4# for polyurethane foam, 10g of foam stabilizer L6900, 200g of foaming agent 141b and 6g of water are fully and uniformly mixed.
And B component: 16g of catalystPMDETA, 19g catalystSP70, 79g curing agentPACM, 90g curing agentThe IPDA is mixed thoroughly and homogeneously.
Respectively and uniformly mixing A, B at 25 ℃ by using a spraying machine, and mixing A, B, C according to the mass ratio (A + B): c is 1: 1.5, mixing uniformly and spraying the mixture on the wall surface of a cold storage, foaming and curing at 25 ℃ to obtain the polyurethane foam plastics, wherein the performance test results are shown in tables 1 and 2.
[ example 10 ]
Polyurethane foams were prepared as follows:
separately, A, B, C components were prepared:
the component A comprises: 580g of polyether polyol 5# for polyurethane foam, 10g of foam stabilizer B8545, 200g of foaming agent CFC-11 and 6g of water are fully and uniformly mixed.
And B component: 16g of catalystPMDETA, 18g catalystSP703, 80g curing agent2110, 90g curing agent8100 mixing well.
Respectively and uniformly mixing A, B at 25 ℃ by using a spraying machine, and mixing A, B, C according to the mass ratio (A + B): c is 1:1.1, mixing uniformly and spraying the mixture on the wall surface of a cold storage directly, foaming and curing at 25 ℃ to obtain the polyurethane foam plastics, wherein the performance test results are shown in tables 1 and 2.
Comparative example 1
Polyether polyol # 6 was prepared according to the method of example 1, except that:
the polyphosphoric acid is not diluted by absolute ethyl alcohol solvent and is directly mixed with polyether polyolR2403. The reactant is changed from colorless to colorless in a short timeThe dark brown color turns into black again, slight charring occurs, and the target product cannot be obtained.
Comparative example 2
Polyether polyol # 7 was prepared according to the method of example 1, except that:
phosphorus atom and polyether polyol in polyphosphoric acidThe molar ratio of hydroxyl groups in R2403 was 1.05:1 and the amount of epoxy WSR618 was increased simultaneously to 1496g (ensuring a molar ratio of phosphorus atoms to epoxy molecules of 1:1.1, as in example 1).
The polyurethane foam was prepared by using polyether polyol # 7 in the same manner as in example 6, and the mixed system of A, B, C was not foamed, and thus polyurethane foam could not be obtained because the amount of polyphosphoric acid was excessive and most of the hydroxyl groups in polyether polyol were consumed by polyphosphoric acid (the hydroxyl value of polyether polyol before and after the reaction was reduced from 760mgKOH/g to 3mgKOH/g), and the resulting polyether polyol # 7 could not be foamed.
Comparative example 3
Polyether polyol # 8 was prepared according to the method of example 1, except that:
phosphorus atom and polyether polyol in polyphosphoric acidThe molar ratio of hydroxyl groups in R2403 is 1:2.5 (the hydroxyl value of polyether polyol before and after reaction is reduced from 760mgKOH/g to 504mgKOH/g), and the dosage of the epoxy resin WSR618 is synchronously reduced to 599g (ensuring that the molar ratio of phosphorus atoms to epoxy resin molecules is 1:1.1, the same as in example 1).
The results of the performance tests on the polyurethane foam epoxy resin compositions obtained in this comparative example are shown in Table 1.
Comparative example 4
A polyurethane foam was prepared as in example 6, except that:
with unmodified conventional polyether polyolsR2403 replaces polyether polyol # 1 for polyurethane foam in the A component, and the performance test results of the polyurethane foam obtained in this comparative example are shown in Table 1.
The polyurethane foams prepared in examples 6 to 10 and comparative examples 3 to 4 were subjected to the tests for compressive strength, dimensional stability, water absorption, solvent resistance and flame retardancy, and the test results are shown in tables 1 and 2:
TABLE 1 partial Performance test results for polyurethane foams
TABLE 2 results of solvent resistance test of polyurethane foams
Eta (hydrochloric acid) /) | Eta (acetic acid)/%) | Eta (ethanol) /) | |
Example 6 | 15 | 65 | 38 |
Example 7 | 17 | 64 | 40 |
Example 8 | 18 | 63 | 39 |
Example 9 | 19 | 68 | 35 |
Example 10 | 17 | 70 | 42 |
Comparative example 3 | 24 | 81 | 52 |
Comparative example 4 | 35 | 103 | 69 |
And (4) analyzing results:
examples 6-10 polyurethane foams were prepared using the polyether polyol prepared according to the present invention, and comparative example 4 polyurethane foams were prepared using an unmodified conventional polyether polyol, as can be seen from Table 1, the compressive strength and dimensional stability of examples 6-10 were greatly improved as compared to comparative example 4. In comparative example 3, since the feed molar ratio of phosphorus atoms to hydroxyl groups of polyether polyol in step S1 was less than 1:2.2, the amount of polyphosphoric acid was relatively small, the degree of reaction was reduced, the effect of modifying polyether polyol with epoxy resin was limited, and the compressive strength and dimensional stability were slightly inferior to those of examples 6 to 10.
The lower the water absorption of the polyurethane foam, the better the hydrophobicity, and as can be seen from table 1, the comparative example 4 shows that the hydrophobicity of examples 6-10 is obviously improved, and the improvement of the hydrophobicity can effectively alleviate the problem that the foam absorbs moisture and bulges in rainy days.
The oxygen index can represent the flame retardant property of the polyurethane foam, and the higher the oxygen index is, the better the flame retardant property is. As can be seen from Table 1, the flame retardant properties of examples 6-10 also have significant advantages over comparative example 4; the solvent resistance is characterized by the magnitude of η, the greater η, the more solvent imbibed within the plastic and the poorer the solvent resistance, as can be seen from table 2, the superior solvent resistance compared to comparative example 4, examples 6-10. The flame retardant and solvent resistance of comparative example 3 is slightly inferior to that of examples 6-10.
In conclusion, the polyether glycol provided by the invention is used as a raw material to prepare polyurethane foam plastics, so that the polyurethane foam plastics have excellent mechanical property, dimensional stability, solvent resistance and flame retardance, and the problem that the foam plastics absorb moisture and swell in rainy days can be effectively solved.
The above description is only a preferred embodiment of the present invention, and it should be noted that, for those skilled in the art, several modifications and additions can be made without departing from the method of the present invention, and these modifications and additions should also be regarded as the protection scope of the present invention.
Claims (10)
1. A preparation method of polyether polyol for polyurethane foam is characterized by comprising the following steps:
s1, carrying out phosphorylation modification on polyether polyol by polyphosphoric acid to generate polyether polyol phosphate, wherein the polyether polyol phosphate contains partial hydroxyl;
and S2, epoxidizing and modifying the polyether polyol phosphate obtained in the step S1 by using epoxy resin to generate the polyether polyol for the polyurethane foam, wherein the molecular structure of the epoxy resin contains benzene rings.
2. The method according to claim 1, wherein the polyether polyol in step S1 has the following formula (II):
wherein R is1Is alkyl or hydrogen, n is the polymerization degree of polyether polyol, x is the functionality of an initiator used for preparing the polyether polyol shown in the formula (II), x is more than or equal to 3, and Y is the structure of the initiator after active hydrogen is removed.
3. The method according to claim 1, wherein in step S1, the ratio of the polyphosphoric acid to the polyether polyol is controlled to be 1 (1.8-2.2) in terms of the molar ratio of phosphorus atoms in the polyphosphoric acid to hydroxyl groups in the polyether polyol;
preferably, in step S1, the polyphosphoric acid is diluted with a solvent before feeding, and added dropwise to the reaction system after dilution; preferably, the mass ratio of the polyphosphoric acid to the solvent is 1: (0.8 to 1.2);
more preferably, the solvent is selected from one or more of ethanol, dichloromethane, chloroform, dimethyl carbonate, methyl acetate and ethyl acetate.
4. The preparation method according to claim 3, wherein in step S1, the temperature of the reaction system is preheated to 50-60 ℃ in advance, and after the temperature of the reaction system is stabilized, the temperature is raised to 75-85 ℃ for reaction for 2-6 hours.
5. The method according to claim 4, wherein the post-treatment operation after the reaction of step S1 comprises: the resulting product was extracted with ethyl acetate and the organic phase was retained, then washed with deionized water and repeatedThe extraction and the washing are carried out for a plurality of times until the water phase is dripped into CaCl2No precipitate is separated out from the saturated aqueous solution; and then drying the organic phase, filtering and removing the solvent to obtain the target product polyether polyol phosphate.
6. The method according to any one of claims 1 to 5, wherein in step S2, the epoxy resin is one or more of glycidyl ether type epoxy resin, glycidyl ester type epoxy resin, glycidyl amine type epoxy resin, and alicyclic epoxy resin, each of which has a molecular structure containing a benzene ring.
7. The method according to claim 6, wherein in step S2, the ratio of phosphorus atoms to epoxy resin molecules in the target product obtained in step S1 is 1 (1.0-1.3);
preferably, the reaction of step S2 is carried out at room temperature for a reaction time of 0.5 to 1 hour.
8. Polyether polyol for polyurethane foams, characterized in that it is obtained by the process according to any one of claims 1 to 7.
9. A polyurethane foam obtained from a composition comprising an isocyanate and the polyether polyol for polyurethane foam of claim 8;
preferably, the components comprise A, B, C components, wherein the total mass of the A component and the B component is 100%, and the composition comprises the following components:
the component A comprises:
and B component:
2 to 3.5 weight percent of catalyst,
7-17 wt% of curing agent;
the component C is isocyanate, and the ratio of the total mass of the component A and the component B to the mass of the component C is 1: (1 to 1.7).
10. The use of the polyurethane foam according to claim 9, wherein the polyurethane foam is used in the fields of freezer spraying, pipe insulation, sheet filling, and home appliance insulation.
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