CN104194119B - A kind of life vest and preparation method thereof - Google Patents

A kind of life vest and preparation method thereof Download PDF

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CN104194119B
CN104194119B CN201410420862.XA CN201410420862A CN104194119B CN 104194119 B CN104194119 B CN 104194119B CN 201410420862 A CN201410420862 A CN 201410420862A CN 104194119 B CN104194119 B CN 104194119B
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parts
polyether
life vest
foaming
tribasic
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CN104194119A (en
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倪海霞
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Guangdong Huile Aquatic Amusement Products Co ltd
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    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
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    • C08L23/06Polyethene
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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
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
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    • 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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    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
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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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    • C08J9/14Working-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 physical blowing agent organic
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    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
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    • C08J2203/16Unsaturated hydrocarbons
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Abstract

This application discloses a kind of life vest and preparation method thereof, weigh LDPE, toluene di-isocyanate(TDI), tribasic lead sulfate, polyether-tribasic alcohol, DCP, triethylene diamine, foaming agent, polyoxyalkylene, EVA, diethyl ethylene diamine, crosslinking agent, dibutyl tin laurate, zinc oxide, stannous octoate and stearic acid according to parts by weight proportioning, after plasticating, be molded into blank foaming;Product relative density 0.03 0.05, absorptivity 5 15mg/cm3;Linear shrinkage ratio 1 2%, hot strength 0.4 0.8MPa;Percentage elongation 150 250%, under 80 90 DEG C of high temperature, 24h is unchanged, and at 50 DEG C, 20 24h are unchanged.

Description

A kind of life vest and preparation method thereof
Technical field
The application belongs to life vest preparation technology field, particularly relates to a kind of life vest and preparation method thereof.
Background technology
Life vest, is an overcoat, and proportion relatively water is light, and order wears life vest, and person floats on seawater, up to water activity lifesaving it Effect.The material component of life vest is mainly foamed glue or air blowing bubble.Appearance color mostly is fresh look, such as bright orange, banana Yellow etc., convenient to lifeboat discovery.Life vest, also known as life vest, is a kind of clothes giving first aid to life, the similar vest of design, Using nylon facing material or neoprene (NEOPRENE), buoyant material or inflatable material, reflectorized material etc. is made.One As service life be 5-7, be one of lifesaving appliance on ship, on aircraft.Generally vest type, with foamed plastics or cork Etc. making.Wear and there is enough buoyancy, make drowning people's head to surface.Buoyant material filled type life vest, i.e. uses Nylon cloth or neoprene make fabric, central filler buoyant material.Inflatable life jacket: use intensity height waterproof material manufacture and Become, similar type inflatable life buoy or the principle of water wing.Divide automatic inflation type or passive inflatable.But this life vest should Considerable: definitely to avoid sharp object to expose or gall waterproof layer, hardly imaginable serious consequence can be caused after gas leakage.
Polyethylene (polyethylene is called for short PE) is the aggregated prepared a kind of thermoplastic resin of ethene.Industrially, Also the copolymer of ethene and a small amount of alpha-olefin is included.Polyethylene odorless, nontoxic, feel ceraceous, there is excellent resistance to low temperature, Chemical stability is good, is resistant to the erosion of most of soda acid.Insoluble in common solvent under normal temperature, water imbibition is little, and electrical insulating property is excellent. Polyethylene is crystalline thermoplastic resin.Their chemical constitution, molecular weight, the degree of polymerization and other performances largely all rely on In the polymerization used.Polymerization determines type and the side chain degree of side chain.Degree of crystallinity depends on the alignment degree of part strand The thermal history experienced with it.Polyethylene is very sensitive for environmental stress (chemistry and mechanism), and heat-resistant aging is worse than The chemical constitution of polymer and processing bar.Polyethylene can be processed with the forming method (see plastic processing) of general thermoplastic.With The most quite varied, it is mainly used to manufacture film, packaging material, container, pipeline, monofilament, electric wire, commodity etc., and Can be as the high-frequency insulation material of TV, radar etc..Along with the development of petrochemical industry, polyethylene production is developed rapidly, produces Amount accounts for the 1/4 of plastics total output.Nineteen eighty-three world's polyethylene total productive capacity is 24.65Mt, is 3.16Mt building device capability. Recent statistics result in 2011, whole world production capacity reaches 96Mt, and the development trend of polyethylene production shows, productive consumption is progressively to Asia Area, continent is shifted, and China day by day becomes most important consumption market.Polyethylene (PE) plastics are a kind of, the convenient bag that we usually carry It is exactly polyethylene (PE).Polyethylene is the simplest macromolecule of structure, is also most widely used macromolecular material.It is by weight Multiple CH2 unit is formed by connecting.Polyethylene is the generation polyaddition reaction by ethene (CH2=CH2). LLDPE application has penetrated into all LDPE market the most.Present stage LLDPE and HDPE is in the growth rank of life cycle Section;LDPE then progresses into the full-fledged phase in 1980 generation ends, and the rarest LDPE equipment is gone into operation.Polyethylene can be with squeezing Go out, inject, mold, be blow molded and the shaping of the method such as melt-spun, be widely used in industry, agricultural, packaging and daily industry, China's application is quite extensive, and film is the user of its maximum, about consumption low density polyethylene (LDPE) 77%, the 18% of high density polyethylene (HDPE), It addition, injection-molded item, electric wire, hollow product etc. all occupy bigger ratio, in its consumption structure in plastics industry Occupy very important status.Polyethylene is typical thermoplastic, is odorless, tasteless, nontoxic flammable white powder. The PE resin of processing and forming is all the wax-like particulate material of extruded granulation, and outward appearance is creamy white.Its molecular weight is at 10,000 one loa ten thousand In the range of.Molecular weight is then ultra-high molecular weight polyethylene f UHMWPE3 more than 100,000.Molecular weight is the highest, its physical mechanics property Can be the best, closer to the requirement level of engineering material.But molecular weight is the highest, the difficulty of its processing increases the most therewith.Polyethylene melts Point is excellent for its resistance to low temperature of 10---130C.At one 60 DEG C, still can keep good mechanical property, but use temperature to exist 80~110 DEG C.Polyethylene chemical stability is preferable, be resistant under room temperature dust technology, dilute sulfuric acid and the hydrochloric acid of any concentration, hydrofluoric acid, The solution such as phosphoric acid, formic acid, acetic acid, ammoniacal liquor, amine, hydrogen peroxide, NaOH, potassium hydroxide.But not powerful oxidation corrosion resistance Corrosion, such as the mixed liquor of oleum red fuming nitric acid (RFNA), chromic acid and sulfuric acid.Polyethylene can be produced slowly by the most above-mentioned solvent Corrosion function, and at 90---100 DEG C, the concentrated sulfuric acid and red fuming nitric acid (RFNA) can corrode polyethylene rapidly so that it is destroy or decompose. Polyethylene is under the effect of air, sunlight and oxygen, it may occur that aging, variable color, chaps, becomes fragile or efflorescence, loses its mechanical property Energy.At a temperature of processing and forming, also can be because of oxidation so that it is melt degree of killing declines, there is variable color, striped occurs, so Attention is should give when processing and forming and use process or selection.Just because of polyethylene has as above speciality, it is easily worked shaping, Therefore the regeneration of polyethylene is reclaimed and is had the most far-reaching value.
Low density polyethylene (LDPE) (LDPE) is a kind of plastic material, and it is suitable for the various moulding process of thermoplastic molding's processing, shaping Processability is good.LDPE is mainly used for making film product, is additionally operable to injection-molded item, medical apparatus, medicine and packaging for foodstuff material Material, blowing hollow molding goods etc..Generally, LLDPE resin density and melt index (MI) characterize.Density is by polymer chain The concentration of comonomer determines.The concentration of comonomer determines the short-chain branch amount in polymer.The length of short-chain branch then depends on The type of comonomer.Comonomer concentration is the highest, and the density of resin is the lowest.Additionally, melt index (MI) is resin mean molecule quantity Reflection, mainly by reaction temperature (solwution method) and add chain-transferring agent (vapor phase method) determine.Mean molecule quantity and molecule Amount distribution is unrelated, and the latter is mainly affected by catalyst type, due to domestic large-scale production hexene, the octene of there is no, and import price Lattice are more expensive, and therefore, the LLDPE resin of domestic production now mainly uses butylene as comonomer.Some enterprise domestic is introducing Though during LLDPE process units, useful hexene makees the trade mark of comonomer, but has to abandon, only because of domestic production without hexene eventually The a small amount of hexene of import when driving examination.The high-grade LLDPE of China's import mostly is this series products.Anticipated to 1-hexene it is from now on The LLDPE demand of monomer will increase by a fairly big margin.And popularizing along with humanity concept, and the composition of novel harmonious society, design Life vest that a kind of absorptivity is low, hot strength is high, linear shrinkage ratio is low and percentage elongation is high and preparation method thereof is the most necessary 's.
Summary of the invention
Solve the technical problem that:
The application is for above-mentioned technical problem, it is provided that a kind of life vest and preparation method thereof, solves existing life vest absorptivity The technical problem such as high, hot strength is low, linear shrinkage ratio is high and percentage elongation is low.
Technical scheme:
A kind of life vest, the raw materials by weight portion proportioning of described life vest is as follows: LDPE100 part;Toluene di-isocyanate(TDI) 40-50 Part;Tribasic lead sulfate 3-5 part;Polyether-tribasic alcohol 40-50 part;DCP1.2-1.8 part;Triethylene diamine 0.3-0.5 part; Foaming agent 20-40 part;Polyoxyalkylene 3-5 part;EVA35-55 part;Diethyl ethylene diamine is 0.6-1 part;Crosslinking agent 0.1-0.5 Part;Dibutyl tin laurate is 0.2-0.6 part;Zinc oxide 5-25 part;Stannous octoate 0.2-0.8 part;Stearic acid 2-8 part.
As a preferred technical solution of the present invention: the raw materials by weight portion proportioning of described life vest is as follows: LDPE100 part; Toluene di-isocyanate(TDI) 42-48 part;Tribasic lead sulfate 3.5-4.5 part;Polyether-tribasic alcohol 44-46 part;DCP1.4-1.6 part; Triethylene diamine 0.35-0.45 part;Foaming agent 25-35 part;Polyoxyalkylene 3.5-4.5 part;EVA40-50 part;Diethyl second Hydramine is 0.7-0.9 part;Crosslinking agent 0.2-0.4 part;Dibutyl tin laurate is 0.3-0.5 part;Zinc oxide 10-20 part; Stannous octoate 0.4-0.6 part;Stearic acid 3-7 part.
As a preferred technical solution of the present invention: the raw materials by weight portion proportioning of described life vest is as follows: LDPE100 part; Toluene di-isocyanate(TDI) 45 parts;Tribasic lead sulfate 4 parts;Polyether-tribasic alcohol 45 parts;DCP1.5 part;Triethylene diamine 0.4 Part;Foaming agent 30 parts;Polyoxyalkylene 4 parts;EVA45 part;Diethyl ethylene diamine is 0.8 part;Crosslinking agent 0.3 part;February Dilaurylate is 0.4 part;15 parts of zinc oxide;Stannous octoate 0.5 part;Stearic acid 5 parts.
As a preferred technical solution of the present invention: described foaming agent uses fluoro trichloromethane or AC foaming agent.
As a preferred technical solution of the present invention: described crosslinking agent uses N-aminoethyl ethanolamine or polyether triol.
As a preferred technical solution of the present invention: the preparation method of described life vest, comprise the steps:
The first step: according to parts by weight proportioning weigh LDPE, toluene di-isocyanate(TDI), tribasic lead sulfate, polyether-tribasic alcohol, DCP, triethylene diamine, foaming agent, polyoxyalkylene, EVA, diethyl ethylene diamine, crosslinking agent, two bays Acid dibutyl tin, zinc oxide, stannous octoate and stearic acid;
Second step: first by LDPE at the mixing 4-8min of plasticator, plasticating temperature 110-130 DEG C, treats LDPE plasticizing in flakes, adds Enter toluene di-isocyanate(TDI), tribasic lead sulfate, polyether-tribasic alcohol and foaming agent be cooled to 80-100 DEG C mixing 8-12min, adds surplus stock, mixing 6-10min at 80-110 DEG C;
3rd step: be molded into blank, loads mould the material after mixing, is warming up to 150-170 DEG C, at pressure 0.6-0.8MPa Lower mold pressing 14-18min, after being cooled to 20-40 DEG C, takes out blank;
4th step: foaming, loads blank in the mould of foaming, foams at 200-220 DEG C, heat 10-15min, Foaming.
Beneficial effect:
A kind of life vest of the present invention and preparation method thereof uses above technical scheme compared with prior art, has techniques below Effect: 1, product relative density 0.03-0.05, absorptivity 5-15mg/cm3;2, linear shrinkage ratio 1-2%, hot strength 0.4-0.8MPa;3, percentage elongation 150-250%, under 80-90 DEG C of high temperature, 24h is unchanged;4, cold resistance is good, 20-24h at-50 DEG C Unchanged, can be with the widespread production not division of history into periods for current material.
Detailed description of the invention
Embodiment 1:
LDPE100 part is weighed according to parts by weight proportioning;Toluene di-isocyanate(TDI) 40 parts;Tribasic lead sulfate 3 parts;Polyethers three Unit's alcohol 40 parts;DCP1.2 part;Triethylene diamine 0.3 part;Fluoro trichloromethane 20 parts;Polyoxyalkylene 3 parts;EVA35 part; Diethyl ethylene diamine is 0.6 part;N-aminoethyl ethanolamine 0.1 part;Dibutyl tin laurate is 0.2 part;5 parts of zinc oxide; Stannous octoate 0.2 part;Stearic acid 2 parts.
First by LDPE at the mixing 4min of plasticator, plasticating temperature 110 DEG C, treat LDPE plasticizing in flakes, add toluene diisocynate Ester, tribasic lead sulfate, polyether-tribasic alcohol and foaming agent are cooled to 80 DEG C of mixing 8min, add surplus stock, at 80 DEG C Mixing 6min.
It is molded into blank, the material after mixing is loaded mould, is warming up to 150 DEG C, under pressure 0.6MPa, mold 14min, After being cooled to 20 DEG C, take out blank;Foaming, loads blank in the mould of foaming, foams, add at 200 DEG C Hot 10min, foaming.
Product relative density 0.05, absorptivity 15mg/cm3;Linear shrinkage ratio 2%, hot strength 0.4MPa;Percentage elongation 150%,
Under 80 DEG C of high temperature, 24h is unchanged, and at-50 DEG C, 20h is unchanged.
Embodiment 2:
LDPE100 part is weighed according to parts by weight proportioning;Toluene di-isocyanate(TDI) 50 parts;Tribasic lead sulfate 5 parts;Polyethers three Unit's alcohol 50 parts;DCP1.8 part;Triethylene diamine 0.5 part;Fluoro trichloromethane 40 parts;Polyoxyalkylene 5 parts;EVA55 part; Diethyl ethylene diamine is 1 part;N-aminoethyl ethanolamine 0.5 part;Dibutyl tin laurate is 0.6 part;25 parts of zinc oxide; Stannous octoate 0.8 part;Stearic acid 8 parts.
First by LDPE at the mixing 8min of plasticator, plasticating temperature 130 DEG C, treat LDPE plasticizing in flakes, add toluene diisocynate Ester, tribasic lead sulfate, polyether-tribasic alcohol and foaming agent are cooled to 100 DEG C of mixing 12min, add surplus stock, at 110 DEG C Under mixing 10min.
It is molded into blank, the material after mixing is loaded mould, is warming up to 170 DEG C, under pressure 0.8MPa, mold 18min, After being cooled to 40 DEG C, take out blank;Foaming, loads blank in the mould of foaming, foams, add at 220 DEG C Hot 15min, foaming.
Product relative density 0.045, absorptivity 8mg/cm3;Linear shrinkage ratio 1.8%, hot strength 0.5MPa;Percentage elongation 180%, under 82 DEG C of high temperature, 24h is unchanged, and at-50 DEG C, 21h is unchanged.
Embodiment 3:
LDPE100 part is weighed according to parts by weight proportioning;Toluene di-isocyanate(TDI) 42 parts;Tribasic lead sulfate 3.5 parts;Polyethers Trihydroxylic alcohol 44 parts;DCP1.4 part;Triethylene diamine 0.35 part;AC foaming agent 25 parts;Polyoxyalkylene 3.5 parts;EVA40 Part;Diethyl ethylene diamine is 0.7 part;N-aminoethyl ethanolamine 0.2 part;Dibutyl tin laurate is 0.3 part;Zinc oxide 10 parts;Stannous octoate 0.4 part;Stearic acid 3 parts.
First by LDPE at the mixing 5min of plasticator, plasticating temperature 115 DEG C, treat LDPE plasticizing in flakes, add toluene diisocynate Ester, tribasic lead sulfate, polyether-tribasic alcohol and foaming agent are cooled to 85 DEG C of mixing 9min, add surplus stock, at 90 DEG C Mixing 7min.
It is molded into blank, the material after mixing is loaded mould, is warming up to 155 DEG C, under pressure 0.65MPa, mold 15min, After being cooled to 25 DEG C, take out blank;Foaming, loads blank in the mould of foaming, foams, add at 205 DEG C Hot 12min, foaming.
Product relative density 0.04, absorptivity 10mg/cm3;Linear shrinkage ratio 1.5%, hot strength 0.6MPa;Percentage elongation 200%, under 85 DEG C of high temperature, 24h is unchanged, and at-50 DEG C, 22h is unchanged.
Embodiment 4:
LDPE100 part is weighed according to parts by weight proportioning;Toluene di-isocyanate(TDI) 48 parts;Tribasic lead sulfate 4.5 parts;Polyethers Trihydroxylic alcohol 46 parts;DCP1.6 part;Triethylene diamine 0.45 part;AC foaming agent 35 parts;Polyoxyalkylene 4.5 parts;EVA50 Part;Diethyl ethylene diamine is 0.9 part;Polyether triol 0.4 part;Dibutyl tin laurate is 0.5 part;20 parts of zinc oxide; Stannous octoate 0.6 part;Stearic acid 7 parts.
First by LDPE at the mixing 7min of plasticator, plasticating temperature 125 DEG C, treat LDPE plasticizing in flakes, add toluene diisocynate Ester, tribasic lead sulfate, polyether-tribasic alcohol and foaming agent are cooled to 95 DEG C of mixing 11min, add surplus stock, at 100 DEG C Under mixing 9min.
It is molded into blank, the material after mixing is loaded mould, is warming up to 165 DEG C, under pressure 0.75MPa, mold 17min, After being cooled to 35 DEG C, take out blank;Foaming, loads blank in the mould of foaming, foams, add at 215 DEG C Hot 14min, foaming.
Product relative density 0.035, absorptivity 12mg/cm3;Linear shrinkage ratio 1.2%, hot strength 0.7MPa;Percentage elongation 220%, under 88 DEG C of high temperature, 24h is unchanged, and at-50 DEG C, 23h is unchanged.
Embodiment 5:
LDPE100 part is weighed according to parts by weight proportioning;Toluene di-isocyanate(TDI) 45 parts;Tribasic lead sulfate 4 parts;Polyethers three Unit's alcohol 45 parts;DCP1.5 part;Triethylene diamine 0.4 part;AC foaming agent 30 parts;Polyoxyalkylene 4 parts;EVA45 part;Two Ehtylethanolamine is 0.8 part;Polyether triol 0.3 part;Dibutyl tin laurate is 0.4 part;15 parts of zinc oxide;Octanoic acid is sub- 0.5 part of tin;Stearic acid 5 parts.
First by LDPE at the mixing 6min of plasticator, plasticating temperature 120 DEG C, treat LDPE plasticizing in flakes, add toluene diisocynate Ester, tribasic lead sulfate, polyether-tribasic alcohol and foaming agent are cooled to 90 DEG C of mixing 10min, add surplus stock, at 95 DEG C Mixing 8min.
It is molded into blank, the material after mixing is loaded mould, is warming up to 160 DEG C, under pressure 0.7MPa, mold 16min, After being cooled to 30 DEG C, take out blank;Foaming, loads blank in the mould of foaming, foams, add at 210 DEG C Hot 13min, foaming.
Product relative density 0.03, absorptivity 5mg/cm3;Linear shrinkage ratio 1%, hot strength 0.8MPa;Percentage elongation 250%, Under 90 DEG C of high temperature, 24h is unchanged, and at-50 DEG C, 24h is unchanged.
Composition all components in above example all can be commercially available.
Above-described embodiment is only intended to be illustrated present disclosure rather than limit, and therefore wants in the right with the present invention Ask any change in the implication and scope that book is suitable, be all considered as being included within the scope of the claims.

Claims (4)

1. a life vest, it is characterised in that the raw materials by weight portion proportioning of described life vest is as follows: LDPE100 part;Toluene di-isocyanate(TDI) 40-50 part;Tribasic lead sulfate 3-5 part;Polyether-tribasic alcohol 40-50 part;DCP1.2-1.8 part;Triethylene diamine 0.3-0.5 part;Fluoro trichloromethane or AC foaming agent 20-40 part;Polyoxyalkylene 3-5 part;EVA35-55 part;Diethyl ethylene diamine is 0.6-1 part;Crosslinking agent N-aminoethyl ethanolamine or polyether triol 0.1-0.5 part;Dibutyl tin laurate is 0.2-0.6 part;Zinc oxide 5-25 part;Stannous octoate 0.2-0.8 part;Stearic acid 2-8 part.
A kind of life vest the most according to claim 1, it is characterised in that described life vest raw materials by weight portion proportioning is as follows: LDPE100 part;Toluene di-isocyanate(TDI) 42-48 part;Tribasic lead sulfate 3.5-4.5 part;Polyether-tribasic alcohol 44-46 part;DCP1.4-1.6 part;Triethylene diamine 0.35-0.45 part;Fluoro trichloromethane or AC foaming agent 25-35 part;Polyoxyalkylene 3.5-4.5 part;EVA40-50 part;Diethyl ethylene diamine is 0.7-0.9 part;Crosslinking agent N-aminoethyl ethanolamine or polyether triol 0.2-0.4 part;Dibutyl tin laurate is 0.3-0.5 part;Zinc oxide 10-20 part;Stannous octoate 0.4-0.6 part;Stearic acid 3-7 part.
A kind of life vest the most according to claim 1, it is characterised in that the raw materials by weight portion proportioning of described life vest is as follows: LDPE100 part;Toluene di-isocyanate(TDI) 45 parts;Tribasic lead sulfate 4 parts;Polyether-tribasic alcohol 45 parts;DCP1.5 part;Triethylene diamine 0.4 part;Fluoro trichloromethane or AC foaming agent 30 parts;Polyoxyalkylene 4 parts;EVA45 part;Diethyl ethylene diamine is 0.8 part;Crosslinking agent N-aminoethyl ethanolamine or polyether triol 0.3 part;Dibutyl tin laurate is 0.4 part;15 parts of zinc oxide;Stannous octoate 0.5 part;Stearic acid 5 parts.
4. the preparation method of life vest described in a claim 1, it is characterised in that comprise the steps:
The first step: weigh LDPE, toluene di-isocyanate(TDI), tribasic lead sulfate, polyether-tribasic alcohol, DCP, triethylene diamine, fluoro trichloromethane or AC foaming agent, polyoxyalkylene, EVA, diethyl ethylene diamine, crosslinking agent N-aminoethyl ethanolamine or polyether triol, dibutyl tin laurate, zinc oxide, stannous octoate and stearic acid according to parts by weight proportioning;
Second step: first by LDPE at the mixing 4-8min of plasticator, plasticating temperature 110-130 DEG C, treat LDPE plasticizing in flakes, add toluene di-isocyanate(TDI), tribasic lead sulfate, polyether-tribasic alcohol and foaming agent and be cooled to 80-100 DEG C of mixing 8-12min, add surplus stock, mixing 6-10min at 80-110 DEG C;
3rd step: be molded into blank, loads mould the material after mixing, is warming up to 150-170 DEG C, molds 14-18min under pressure 0.6-0.8MPa, after being cooled to 20-40 DEG C, takes out blank;
4th step: foaming, loads blank in the mould of foaming, foams at 200-220 DEG C, heat 10-15min, foaming.
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CN106519381A (en) * 2016-11-02 2017-03-22 天津毅兴彩科技有限公司 A plastic life jacket used for ships and a preparing method thereof
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