CN107746474A - A kind of preparation method of the EU sponge with flame-proof antibiotic function - Google Patents

A kind of preparation method of the EU sponge with flame-proof antibiotic function Download PDF

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CN107746474A
CN107746474A CN201710973099.7A CN201710973099A CN107746474A CN 107746474 A CN107746474 A CN 107746474A CN 201710973099 A CN201710973099 A CN 201710973099A CN 107746474 A CN107746474 A CN 107746474A
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sponge
carbonic acid
surface coating
ppg
flame
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卢伟
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DEQING SHUHUA BUBBLE CHAIR Co Ltd
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DEQING SHUHUA BUBBLE CHAIR Co Ltd
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    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/0061Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
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    • 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
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    • 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
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    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/06Working-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
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    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/06Working-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
    • C08J9/10Working-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 nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
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    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
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    • C08K5/42Sulfonic acids; Derivatives thereof
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    • C08J2483/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
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Abstract

The invention belongs to polyurethane sponge technical field.The invention discloses a kind of preparation method of the EU sponge with flame-proof antibiotic function, it includes the steps such as composite foamable agent preparation, stock, dispensing, batch mixing, feeding and foaming, wherein employ the composite foamable agent formed with Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide, Surface coating carbonic acid hydrogen sodium is coated on made from sodium acid carbonate surface by silicone Quaternary Ammonium Salt Antimicrobial Agent, and Surface coating carbonic acid ammonium is coated on made from ammonium carbonate surface by perfluorobutyl potassium sulfonate.There is low resilience, neither too hard, nor too soft by EU sponge produced by the present invention, there is fine flame retardant effect;To having carried out special antimicrobial treatment in the duct of EU sponge, solves the problems, such as in sponge duct the easily harmful microorganism such as growth/enrichment of bacterial.

Description

A kind of preparation method of the EU sponge with flame-proof antibiotic function
Technical field
The present invention relates to polyurethane sponge technical field, gathers more particularly, to a kind of polyether-type with flame-proof antibiotic function The preparation method of urethane sponge.
Background technology
Sponge refers to all expanded materials, and resin, rubber, the foaming product of plastics all claim sponge.Polyurethane sponge is exactly Foamed polyurethane material.The elasticity of the existing rubber of polyurethane, there are the intensity of plastics and excellent processing characteristics again, can be used to prepare Polyurethane low resilience urethane foam resilient foam(Flexible polyurethane foams).
Polyol starting material point of the flexible polyurethane foam to use, the soft bubble of polyester-type and the soft bubble of polyether-type can be divided into. EU is a kind of open eucaryotic cell structure, the characteristic with warming decompression, be may also be referred to as to be a kind of warming Pressure drop materials.
As a kind of macromolecule organic foam material, the flammable properties of EU sponge, which become, threatens its safety A major issue, therefore it is flame-retardant modified to have made some to EU sponge on existing market;As Chinese patent is public Cloth CN102643404A, patent disclosure day are August in 2012 22, a kind of entitled Slow-rebound polyether polyurethane sponge it is special Profit disclose it is a kind of for EU sponge it is inflammable the characteristics of made it is flame-retardant modified, in matching somebody with somebody for EU sponge With the addition of in side sulfonate salt flame carried out it is flame-retardant modified, although its flame retardant effect has obtained certain improvement, due to Its fire retardant single effect added, its flame retardant effect are still difficult to meet the public to EU sponge flame retardant effect It is required that.
The content of the invention
It can obtain with low resilience, neither too hard, nor too soft, have fine to solve the above problems, the invention provides one kind Flame retardant effect, and the preparation method of the EU sponge with antibacterial effect.
To achieve the above object, the technical solution adopted by the present invention is as follows:
A kind of preparation method of the EU sponge with flame-proof antibiotic function, comprises the following steps:
a)Composite foamable agent is prepared:By Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide by weight 1: 1:(1~2)Prepare composite foamable agent;
b)Stock:By 65~75 parts of the first PPG, the second 10~20 parts of PPG, the 3rd PPG 10~ 20 parts, the first 0.45~0.55 part of catalyst, the second 0.05~0.15 part of catalyst, 1.9~2.1 parts of silicone oil, 5~8 parts of rubber, 3.0~4.0 parts of water, 8~12 parts of composite foamable agent, 55~61 parts of MDI isocyanate weigh each component;
c)Dispensing:First PPG, the second PPG and the 3rd PPG are mixed to prepare mixture A, will First catalyst, the second catalyst, silicone oil, water, composite foamable agent, MDI isocyanate are mixed to prepare mixture B;
d)Batch mixing:Mixture A and mixture B are stirred respectively successively mixed liquor A and mixed liquid B is made;
e)Feeding:After temperature in mould to be foamed reaches 50~55 DEG C, feeding capacity is controlled and to mould by formula rate In feed mixed liquor A, mixed liquid B, rubber;
f)Foaming:Foamed 1~10 minute in 50~55 DEG C of foaming mould, and it is cold after being incubated 1~5 hour at 30~40 DEG C But the EU sponge with flame-proof antibiotic function is made.
Preferably, the first PPG is PPG 1621, the second PPG is polyethers GLR-2000, 3rd PPG is polyethers GPOP-36/30, and the first catalyst is catalyst A33, and the second catalyst is catalyst A1.
PPG 1621 is a kind of base polyester raw material of the common slow-rebound foaming sponge of in the market, polyethers GLR- 2000 and polyethers GPOP-36/30 is two kinds of the production of Shanghai Gaoqiao petrochemical industry Co., Ltd without slow-rebound foamings of the BHT without amine The base polyester raw material of sponge;Catalyst A33 is the DPG solution of 33% triethylene diamine, and catalyst A1 is double(Diformazan ammonia Base ethyl)Ether is with dipropylene glycol with weight than 7:3 solution prepared, above two catalyst is all to be used for poly- ammonia on the market The conventional catalyst of ester production;Foaming agent 141b is a fluorine dichloroethanes.
Preferably, rubber is made up of silicon rubber and nitrile rubber, wherein the weight percentage of nitrile rubber be 20~ 30%, surplus is silicon rubber.
Silicon rubber and nitrile rubber are the synthetic rubber for having high resiliency feature, and being properly added in polyurethane sponge can be with So that polyurethane has preferably elasticity.Silicon rubber has good weather resistance, and can extend polyurethane sponge uses the longevity Life;Nitrile rubber, there is the features such as chemical-resistant stability energy is good, and antistatic property is good, the cold resistance of polyurethane sponge can be improved The performances such as energy, chemical-resistant stability.
Preferably, composite foamable agent presses weight by Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide Measure ratio 1:1:(1~1.5)Composition.
Azodicarbonamide is a kind of organic foaming agent, but it foams(Decompose in other words)Temperature is too high, therefore is adding A certain amount of ammonium carbonate and sodium acid carbonate are added while azodicarbonamide, is reduced by the mixing with sodium acid carbonate and ammonium carbonate The decomposition temperature of azodicarbonamide, blowing temperature is reduced, meanwhile, sodium acid carbonate and ammonium carbonate are also easily thermally decomposed, and can also be risen To the effect of foaming;Due to the most high-molecular organic material of polyurethane sponge raw material, sodium acid carbonate, the phase of ammonium carbonate and each raw material Dissolubility is poor, can be more preferable in the present invention before use, first carry out Surface coating processing to sodium acid carbonate and ammonium carbonate Combined with each raw material in polyurethane sponge, ensure the distribution that foaming agent can be evenly, and improve foaming effect.
It is made preferably, Surface coating carbonic acid hydrogen sodium is coated on sodium acid carbonate surface by silicone Quaternary Ammonium Salt Antimicrobial Agent 's.
Organosilicon quaternary ammonium salt is a kind of organic antibacterial agent, simultaneously because its molecular characterization its still can also be considered one kind Surface modifier, after coating sodium acid carbonate using silicone Quaternary Ammonium Salt Antimicrobial Agent, modified sodium acid carbonate is enabled to gathering The raw material of urethane sponge has more preferable compatibility, can preferably be distributed in the feed, at the same it is coated after sodium acid carbonate Also will not be dissolved in the water of raw material.
Preferably, Surface coating carbonic acid ammonium is coated on made from ammonium carbonate surface by perfluorobutyl potassium sulfonate.
Perfluorobutyl potassium sulfonate is a kind of organic fire-retardant, simultaneously because its molecular characterization, can also be considered as a kind of tool There is the organic matter of surface modifying function, after coating ammonium carbonate with it the ammonium carbonate after cladding can be made to obtain and polyurethane sponge The more preferable compatibility of raw material, make its in the feed it is scattered evenly, while it is coated after ammonium carbonate will not also be dissolved in original In the water of material.
Preferably, Surface coating carbonic acid hydrogen sodium is made by following methods, first silicone Quaternary Ammonium Salt Antimicrobial Agent is dissolved in In the acetone of 1.5~2 times of its weight, the bicarbonate of 2~2.5 times of silicone Quaternary Ammonium Salt Antimicrobial Agent weight is then added thereto again Sodium, then it is ultrasonically treated 10~20 minutes at 20~30 DEG C, Surface coating carbonic acid hydrogen sodium is made after drying.
Preferably, Surface coating carbonic acid ammonium is made by following methods, perfluorobutyl potassium sulfonate is first dissolved in 1.5~2 Again in the acetone of its weight, the ammonium carbonate of 2~2.5 times of perfluorobutyl potassium sulfonate weight is then added thereto again, then 20 It is ultrasonically treated 10~20 minutes at~30 DEG C, Surface coating carbonic acid ammonium is made after drying.
The modification of sodium acid carbonate and ammonium carbonate all by the way that first modifying agent is scattered in acetone, then add sodium acid carbonate or Carry out being ultrasonically treated after ammonium carbonate and be made.Temperature that should be during strict control process when being wherein ultrasonically treated, prevents Yin Wen Height is spent so that sodium acid carbonate or ammonium carbonate are decomposed.
Polyurethane sponge is a kind of material with loose structure, due to its special pore passage structure, is more easy in duct The harmful microorganisms such as enrichment of bacterial, so this kind of material for polyurethane sponge, is more easy to have in mind when carrying out antimicrobial treatment to it Antimicrobial treatment in its duct.In the prior art, antiseptic is uniformly added in raw material, also generally equal after treatment Even is distributed in sea, comparatively just seems it is not that is enough for the antimicrobial treatment in sponge duct;In the present invention Antiseptic is coated on to the surface of inorganic foaming agent, one serves the effect of surfactant so that inorganic foaming agent can Preferably combined with Organic Ingredients, two carry out the decomposition with foaming agent, and the antiseptic on inorganic foaming agent surface is by scattered formation Gas carrier inside sponge to external diffusion, because the duct of polyurethane sponge is that gas acts on as caused by decomposing foaming agent Lower formation, then the antiseptic carried in these gases is also taken advantage of a situation into duct, and with the decline of gas motion speed, Antiseptic is attached in cell walls, is formd the reinforcement for antibacterial action in duct and is handled;Similarly fire retardant is also according to similar Principle be scattered in sponge duct.
Therefore, the invention has the advantages that:
(1)There is low resilience, neither too hard, nor too soft by EU sponge produced by the present invention, there is fine fire-retardant effect Fruit;
(2)Special antimicrobial treatment has been carried out in duct by EU sponge produced by the present invention, has solved sea In continuous duct easily the harmful microorganism such as growth/enrichment of bacterial the problem of.
Embodiment
Technical scheme is further described with reference to embodiment.
Obviously, described embodiment is only the part of the embodiment of the present invention, rather than whole embodiments.Based on this Embodiment in invention, all other reality that those of ordinary skill in the art are obtained under the premise of creative work is not made Example is applied, belongs to the scope of protection of the invention.
In the present invention, if not refering in particular to, all equipment and raw material are commercially available or the industry is conventional, Method in following embodiments, it is this area conventional method unless otherwise instructed.
Embodiment 1
A kind of preparation method of the EU sponge with flame-proof antibiotic function, comprises the following steps:
a)Composite foamable agent is prepared:By Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide by weight 1: 1:1 prepares composite foamable agent;
b)Stock:By 65 parts of the first PPG, the second 10 parts of PPG, the 3rd 10 parts of PPG, first urges 0.45 part of agent, the second 0.05 part of catalyst, 1.9 parts of silicone oil, 5 parts of rubber, 3.0 parts of water, 8 parts of composite foamable agent, MDI isocyanic acids 55 parts of ester weighs each component;First PPG is PPG 1621, and the second PPG is polyethers GLR-2000, 3rd PPG is polyethers GPOP-36/30, and the first catalyst is catalyst A33, and the second catalyst is catalyst A1;Rubber Glue is made up of silicon rubber and nitrile rubber, and wherein the weight percentage of nitrile rubber is 20%, the weight percentage of silicon rubber For 80%;
c)Dispensing:First PPG, the second PPG and the 3rd PPG are mixed to prepare mixture A, will First catalyst, the second catalyst, silicone oil, water, composite foamable agent, MDI isocyanate are mixed to prepare mixture B;
d)Batch mixing:Mixture A and mixture B are stirred respectively successively mixed liquor A and mixed liquid B is made;
e)Feeding:After temperature in mould to be foamed reaches 50 DEG C, control feeding capacity by formula rate and thrown into mould Feed mixed liquor A, mixed liquid B, rubber;
f)Foaming:Foamed 1 minute in 50 DEG C of foaming mould, and cool down and be made with fire-retardant after being incubated 1 hour at 30 DEG C The EU sponge of antibacterial functions;
Wherein, Surface coating carbonic acid hydrogen sodium is coated on made from sodium acid carbonate surface by silicone Quaternary Ammonium Salt Antimicrobial Agent;Surface Cladding sodium acid carbonate is made by following methods, is first dissolved in silicone Quaternary Ammonium Salt Antimicrobial Agent in the acetone of 1.5 times of its weight, so Add the sodium acid carbonate of 2 times of silicone Quaternary Ammonium Salt Antimicrobial Agent weight thereto again afterwards, be then ultrasonically treated 10 minutes at 20 DEG C, Surface coating carbonic acid hydrogen sodium is made after drying;
Surface coating carbonic acid ammonium is coated on made from ammonium carbonate surface by perfluorobutyl potassium sulfonate;Surface coating carbonic acid ammonium by with Lower section method is made, and is first dissolved in perfluorobutyl potassium sulfonate in the acetone of 1.5 times of its weight, then adds 2 times thereto again entirely The ammonium carbonate of fluorine butyl sulfonic acid potassium weight, then it is ultrasonically treated 10 minutes at 20 DEG C, Surface coating carbonic acid ammonium is made after drying.
Embodiment 2
A kind of preparation method of the EU sponge with flame-proof antibiotic function, comprises the following steps:
a)Composite foamable agent is prepared:By Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide by weight 1: 1:1.5 prepare composite foamable agent;
b)Stock:By 72 parts of the first PPG, the second 13 parts of PPG, the 3rd 15 parts of PPG, first urges 0.50 part of agent, the second 0.10 part of catalyst, 2.0 parts of silicone oil, 6 parts of rubber, 3.3 parts of water, 9 parts of composite foamable agent, MDI isocyanic acids 57 parts of ester weighs each component;First PPG is PPG 1621, and the second PPG is polyethers GLR-2000, 3rd PPG is polyethers GPOP-36/30, and the first catalyst is catalyst A33, and the second catalyst is catalyst A1;Rubber Glue is made up of silicon rubber and nitrile rubber, and wherein the weight percentage of nitrile rubber is 23%, the weight percentage of silicon rubber For 77%;
c)Dispensing:First PPG, the second PPG and the 3rd PPG are mixed to prepare mixture A, will First catalyst, the second catalyst, silicone oil, water, composite foamable agent, MDI isocyanate are mixed to prepare mixture B;
d)Batch mixing:Mixture A and mixture B are stirred respectively successively mixed liquor A and mixed liquid B is made;
e)Feeding:After temperature in mould to be foamed reaches 52 DEG C, control feeding capacity by formula rate and thrown into mould Feed mixed liquor A, mixed liquid B, rubber;
f)Foaming:Foamed 4 minutes in 52 DEG C of foaming mould, and cool down and be made with fire-retardant after being incubated 2 hours at 35 DEG C The EU sponge of antibacterial functions;
Wherein, Surface coating carbonic acid hydrogen sodium is coated on made from sodium acid carbonate surface by silicone Quaternary Ammonium Salt Antimicrobial Agent;Surface Cladding sodium acid carbonate is made by following methods, is first dissolved in silicone Quaternary Ammonium Salt Antimicrobial Agent in the acetone of 1.7 times of its weight, so Add the sodium acid carbonate of 2.2 times of silicone Quaternary Ammonium Salt Antimicrobial Agent weight thereto again afterwards, 15 points are then ultrasonically treated at 25 DEG C Clock, Surface coating carbonic acid hydrogen sodium is made after drying;
Surface coating carbonic acid ammonium is coated on made from ammonium carbonate surface by perfluorobutyl potassium sulfonate;Surface coating carbonic acid ammonium by with Lower section method is made, and is first dissolved in perfluorobutyl potassium sulfonate in the acetone of 1.7 times of its weight, then adds 2.2 times thereto again The ammonium carbonate of perfluorobutyl potassium sulfonate weight, then it is ultrasonically treated 15 minutes at 25 DEG C, Surface coating carbonic acid is made after drying Ammonium.
Embodiment 3
A kind of preparation method of the EU sponge with flame-proof antibiotic function, comprises the following steps:
a)Composite foamable agent is prepared:By Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide by weight 1: 1:1.5 prepare composite foamable agent;
b)Stock:By 68 parts of the first PPG, the second 15 parts of PPG, the 3rd 17 parts of PPG, first urges 0.50 part of agent, the second 0.10 part of catalyst, 2.0 parts of silicone oil, 7 parts of rubber, 3.7 parts of water, 11 parts of composite foamable agent, MDI isocyanides 59 parts of acid esters weighs each component;First PPG is PPG 1621, and the second PPG is polyethers GLR- 2000, the 3rd PPG is polyethers GPOP-36/30, and the first catalyst is catalyst A33, and the second catalyst is catalyst A1;Rubber is made up of silicon rubber and nitrile rubber, and wherein the weight percentage of nitrile rubber is 27%, the weight hundred of silicon rubber It is 73% to divide content;
c)Dispensing:First PPG, the second PPG and the 3rd PPG are mixed to prepare mixture A, will First catalyst, the second catalyst, silicone oil, water, composite foamable agent, MDI isocyanate are mixed to prepare mixture B;
d)Batch mixing:Mixture A and mixture B are stirred respectively successively mixed liquor A and mixed liquid B is made;
e)Feeding:After temperature in mould to be foamed reaches 53 DEG C, control feeding capacity by formula rate and thrown into mould Feed mixed liquor A, mixed liquid B, rubber;
f)Foaming:Foamed 7 minutes in 53 DEG C of foaming mould, and cool down and be made with fire-retardant after being incubated 3 hours at 35 DEG C The EU sponge of antibacterial functions;
Wherein, Surface coating carbonic acid hydrogen sodium is coated on made from sodium acid carbonate surface by silicone Quaternary Ammonium Salt Antimicrobial Agent;Surface Cladding sodium acid carbonate is made by following methods, is first dissolved in silicone Quaternary Ammonium Salt Antimicrobial Agent in the acetone of 1.8 times of its weight, so Add the sodium acid carbonate of 2.3 times of silicone Quaternary Ammonium Salt Antimicrobial Agent weight thereto again afterwards, 15 points are then ultrasonically treated at 25 DEG C Clock, Surface coating carbonic acid hydrogen sodium is made after drying;
Surface coating carbonic acid ammonium is coated on made from ammonium carbonate surface by perfluorobutyl potassium sulfonate;Surface coating carbonic acid ammonium by with Lower section method is made, and is first dissolved in perfluorobutyl potassium sulfonate in the acetone of 1.8 times of its weight, then adds 2.3 times thereto again The ammonium carbonate of perfluorobutyl potassium sulfonate weight, then it is ultrasonically treated 15 minutes at 25 DEG C, Surface coating carbonic acid is made after drying Ammonium.
Embodiment 4
A kind of preparation method of the EU sponge with flame-proof antibiotic function, comprises the following steps:
a)Composite foamable agent is prepared:By Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide by weight 1: 1:2 prepare composite foamable agent;
b)Stock:By 75 parts of the first PPG, the second 20 parts of PPG, the 3rd 20 parts of PPG, first urges 0.55 part of agent, the second 0.15 part of catalyst, 2.1 parts of silicone oil, 8 parts of rubber, 4.0 parts of water, 12 parts of composite foamable agent, MDI isocyanides 61 parts of acid esters weighs each component;First PPG is PPG 1621, and the second PPG is polyethers GLR- 2000, the 3rd PPG is polyethers GPOP-36/30, and the first catalyst is catalyst A33, and the second catalyst is catalyst A1;Rubber is made up of silicon rubber and nitrile rubber, and wherein the weight percentage of nitrile rubber is 30%, the weight hundred of silicon rubber It is 70% to divide content;
c)Dispensing:First PPG, the second PPG and the 3rd PPG are mixed to prepare mixture A, will First catalyst, the second catalyst, silicone oil, water, composite foamable agent, MDI isocyanate are mixed to prepare mixture B;
d)Batch mixing:Mixture A and mixture B are stirred respectively successively mixed liquor A and mixed liquid B is made;
e)Feeding:After temperature in mould to be foamed reaches 55 DEG C, control feeding capacity by formula rate and thrown into mould Feed mixed liquor A, mixed liquid B, rubber;
f)Foaming:Foamed 10 minutes in 55 DEG C of foaming mould, and cool down and be made with fire-retardant after being incubated 5 hours at 40 DEG C The EU sponge of antibacterial functions;
Wherein, Surface coating carbonic acid hydrogen sodium is coated on made from sodium acid carbonate surface by silicone Quaternary Ammonium Salt Antimicrobial Agent;Surface Cladding sodium acid carbonate is made by following methods, is first dissolved in silicone Quaternary Ammonium Salt Antimicrobial Agent in the acetone of 2 times of its weight, then Add the sodium acid carbonate of 2.5 times of silicone Quaternary Ammonium Salt Antimicrobial Agent weight thereto again, be then ultrasonically treated 20 minutes at 30 DEG C, Surface coating carbonic acid hydrogen sodium is made after drying;
Surface coating carbonic acid ammonium is coated on made from ammonium carbonate surface by perfluorobutyl potassium sulfonate;Surface coating carbonic acid ammonium by with Lower section method is made, and is first dissolved in perfluorobutyl potassium sulfonate in the acetone of 2 times of its weight, then adds 2.5 times thereto again entirely The ammonium carbonate of fluorine butyl sulfonic acid potassium weight, then it is ultrasonically treated 20 minutes at 30 DEG C, Surface coating carbonic acid ammonium is made after drying.
Characterization result:
For by the EU sponge produced by the present invention with anti-flaming function with fire-retardant, antibacterial and low resilience Corresponding performance test is carried out to it etc. characteristic.
Fire resistance is tested and evaluated using UL94 fire-retardant fireproofs level estimate and standard, wherein in above-described embodiment The EU sponge with anti-flaming function can reach V0 level flame-retardancy requirements;
Anti-microbial property test is with reference to (Counting alive microbial method) TZ/TO2021-9 of AATCC Test Method 100 to above-described embodiment In EU sponge with anti-flaming function carry out antibacterial measure and carry out antimicrobial spectrum measure;Testing result:To large intestine Bacillus, staphylococcus aureus, Candida albicans etc. more than 20, which plants harmful bacteria, efficient rejection ability, and average bacteriostasis rate >= 98%;
Rebound degree test is tested and evaluated using ISO8307-2008 test machine standards, has fire-retardant work(in above-described embodiment The rebound degree of the EU sponge of energy is followed successively by 3.7%, 2.8%, 2.8%, 3.2%, and its low resilience effect is compared to existing Most of product will be outstanding on the market.
It should be appreciated that to those skilled in the art, it can according to the above description be improved or be become Change, and all these modifications and variations should all belong to the protection domain of appended claims of the present invention.

Claims (8)

1. a kind of preparation method of the EU sponge with flame-proof antibiotic function, it is characterised in that including following step Suddenly:
a)Composite foamable agent is prepared:By Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide by weight 1: 1:(1~2)Prepare composite foamable agent;
b)Stock:By 65~75 parts of the first PPG, the second 10~20 parts of PPG, the 3rd PPG 10~ 20 parts, the first 0.45~0.55 part of catalyst, the second 0.05~0.15 part of catalyst, 1.9~2.1 parts of silicone oil, 5~8 parts of rubber, 3.0~4.0 parts of water, 8~12 parts of composite foamable agent, 55~61 parts of MDI isocyanate weigh each component;
c)Dispensing:First PPG, the second PPG and the 3rd PPG are mixed to prepare mixture A, will First catalyst, the second catalyst, silicone oil, water, composite foamable agent, MDI isocyanate are mixed to prepare mixture B;
d)Batch mixing:Mixture A and mixture B are stirred respectively successively mixed liquor A and mixed liquid B is made;
e)Feeding:After temperature in mould to be foamed reaches 50~55 DEG C, feeding capacity is controlled and to mould by formula rate In feed mixed liquor A, mixed liquid B, rubber;
f)Foaming:Foamed 1~10 minute in 50~55 DEG C of foaming mould, and it is cold after being incubated 1~5 hour at 30~40 DEG C But the EU sponge with flame-proof antibiotic function is made.
2. a kind of preparation method of EU sponge with flame-proof antibiotic function according to claim 1, its It is characterised by:
The first described PPG is PPG 1621, and the second described PPG is polyethers GLR-2000, The 3rd described PPG is polyethers GPOP-36/30, and the first described catalyst is catalyst A33, and the second catalyst is Catalyst A1.
3. a kind of preparation method of EU sponge with flame-proof antibiotic function according to claim 1, its It is characterised by:
Described rubber is made up of silicon rubber and nitrile rubber, and wherein the weight percentage of nitrile rubber is 20~30%, surplus For silicon rubber.
4. a kind of preparation method of EU sponge with flame-proof antibiotic function according to claim 1, its It is characterised by:
Described composite foamable agent is by Surface coating carbonic acid hydrogen sodium, Surface coating carbonic acid ammonium and azodicarbonamide by weight 1:1: (1~1.5)Composition.
5. a kind of preparation method of EU sponge with flame-proof antibiotic function according to claim 1, its It is characterised by:
Described Surface coating carbonic acid hydrogen sodium is coated on made from sodium acid carbonate surface by silicone Quaternary Ammonium Salt Antimicrobial Agent.
6. a kind of preparation method of EU sponge with flame-proof antibiotic function according to claim 1, its It is characterised by:
Described Surface coating carbonic acid ammonium is coated on made from ammonium carbonate surface by perfluorobutyl potassium sulfonate.
7. a kind of preparation method of the EU sponge with flame-proof antibiotic function according to claim 1 or 5, It is characterized in that:
Described Surface coating carbonic acid hydrogen sodium is made by following methods, and silicone Quaternary Ammonium Salt Antimicrobial Agent first is dissolved in into 1.5~2 times In the acetone of its weight, the sodium acid carbonate of 2~2.5 times of silicone Quaternary Ammonium Salt Antimicrobial Agent weight is then added thereto again, then It is ultrasonically treated 10~20 minutes at 20~30 DEG C, Surface coating carbonic acid hydrogen sodium is made after drying.
8. a kind of preparation method of EU sponge with flame-proof antibiotic function according to claim 1 or 6, It is characterized in that:
Described Surface coating carbonic acid ammonium is made by following methods, and perfluorobutyl potassium sulfonate first is dissolved in into 1.5~2 times of its weight Acetone in, then again thereto add 2~2.5 times of perfluorobutyl potassium sulfonate weight ammonium carbonate, then at 20~30 DEG C It is ultrasonically treated 10~20 minutes, Surface coating carbonic acid ammonium is made after drying.
CN201710973099.7A 2017-10-18 2017-10-18 A kind of preparation method of the EU sponge with flame-proof antibiotic function Pending CN107746474A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112225941A (en) * 2020-09-24 2021-01-15 杭州传化精细化工有限公司 Flame-retardant antibacterial polyurethane sponge and preparation method thereof
CN113372709A (en) * 2021-07-26 2021-09-10 华侨大学 Preparation method of antibacterial slow-resilience polyurethane sponge

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102643405A (en) * 2012-04-28 2012-08-22 德清舒华泡沫座椅有限公司 Manufacture method for slow-rebound polyether polyurethane sponge
CN107118544A (en) * 2017-05-25 2017-09-01 德清舒华泡沫座椅有限公司 A kind of preparation method with anti-flaming function EU sponge

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102643405A (en) * 2012-04-28 2012-08-22 德清舒华泡沫座椅有限公司 Manufacture method for slow-rebound polyether polyurethane sponge
CN107118544A (en) * 2017-05-25 2017-09-01 德清舒华泡沫座椅有限公司 A kind of preparation method with anti-flaming function EU sponge

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112225941A (en) * 2020-09-24 2021-01-15 杭州传化精细化工有限公司 Flame-retardant antibacterial polyurethane sponge and preparation method thereof
CN112225941B (en) * 2020-09-24 2022-06-24 浙江传化功能新材料有限公司 Flame-retardant antibacterial polyurethane sponge and preparation method thereof
CN113372709A (en) * 2021-07-26 2021-09-10 华侨大学 Preparation method of antibacterial slow-resilience polyurethane sponge

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