CN107603556A - A kind of preparation method of tent PUR - Google Patents

A kind of preparation method of tent PUR Download PDF

Info

Publication number
CN107603556A
CN107603556A CN201710902601.5A CN201710902601A CN107603556A CN 107603556 A CN107603556 A CN 107603556A CN 201710902601 A CN201710902601 A CN 201710902601A CN 107603556 A CN107603556 A CN 107603556A
Authority
CN
China
Prior art keywords
dibasic acid
tent
dimeric dibasic
pur
anhydrous
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201710902601.5A
Other languages
Chinese (zh)
Inventor
温同民
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anhui Jiaming New Mstar Technology Ltd
Original Assignee
Anhui Jiaming New Mstar Technology Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Anhui Jiaming New Mstar Technology Ltd filed Critical Anhui Jiaming New Mstar Technology Ltd
Priority to CN201710902601.5A priority Critical patent/CN107603556A/en
Publication of CN107603556A publication Critical patent/CN107603556A/en
Pending legal-status Critical Current

Links

Landscapes

  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Body Structure For Vehicles (AREA)

Abstract

The present invention discloses a kind of preparation method of tent bonding PUR, including following operating procedure:(1)After dimeric dibasic acid and benzene are mixed, fluidized state is heated under normal pressure, after keeping the 12min of fluidized state 8, room temperature is cooled to, adds anhydrous magnesium sulfate thereto, is evaporated under reduced pressure, anhydrous dimeric dibasic acid is made;(2)Anhydrous dimeric dibasic acid, caprolactam, IPD are added into autoclave, and continue to add sodium phytate, hmds, the concentrated sulfuric acid thereto, after well mixed, the temperature of autoclave is risen to 230 240 DEG C, it is that 1.3 1.5MPa react 160 200min to keep pressure;(3)After pressure release, titanate coupling agent NDZ 201, aluminium isopropoxide are added thereto, and after being well mixed, after the 80min of insulation reaction 60, mixture is down to room temperature, finished product.PUR cohesive force produced by the present invention is strong, and especially it has excellent weatherability, and for tent during use, glue is not susceptible to the phenomenon of failure, effectively extends the service life of tent.

Description

A kind of preparation method of tent PUR
Technical field
The invention belongs to tent preparing technical field, and in particular to a kind of preparation method of tent PUR.
Background technology
Tent is to support to cover wind and rain, daylight and the shed for living temporarily on the ground.Multi-purpose canvas is made, and is used together with support Thing, transfer can be pulled down at any time.The quality of tent quality, mainly determined by the quality of its fabric, it is general commercially available common Tent material up and down two layers be TPUE rubber(TPU)Material, intermediate layer are woven dacron, per shell fabric it Between bonded by PUR.But commercially available common PUR, weatherability is poor, in the wild in use, being easy to aoxidize Act on and bond effect occur, cause tent material the phenomenon departed from occur.
The content of the invention
In order to solve the above-mentioned technical problem, the present invention provides a kind of preparation method of tent PUR.
The present invention is achieved by the following technical solutions.
A kind of preparation method of tent bonding PUR, including following operating procedure:
(1)By dimeric dibasic acid and benzene according to 10-15:After 3 ratio mixing, fluidized state is heated under normal pressure, keeps fluidized state After 8-12min, room temperature is cooled to, is 1 according to mass volume ratio:300 ratio adds anhydrous magnesium sulfate thereto, and decompression is steamed Evaporate, anhydrous dimeric dibasic acid is made;
(2)By weight, by 54-65 part steps(1)The anhydrous dimeric dibasic acid of gained, 34-38 parts caprolactam, 10-15 parts are different Isophoronediamine is added into autoclave, and continues to add 2-4 parts sodium phytate, 4-8 parts hmds, 0.1- thereto 0.3 part of concentrated sulfuric acid, after being well mixed, the temperature of autoclave is risen to 230-240 DEG C, keeps pressure to be reacted for 1.3-1.5MPa 160-200min;
(3)After pressure release, after being cooled to 120-140 DEG C, titanate coupling agent NDZ-201, aluminium isopropoxide are added thereto, is mixed After closing uniformly, after insulation reaction 60-80min, mixture is down to room temperature, finished product.
Specifically, in above-mentioned dimeric dibasic acid, mono-acid content is 4%, dimer content 88%, and tripolymer content is 8%, relatively Molecular mass is 570.
Specifically, above-mentioned steps(3)In, titanate coupling agent NDZ-201 addition is step(2)In anhydrous dimeric dibasic acid The 3-6% of quality, the addition of aluminium isopropoxide is step(2)In anhydrous dimeric dibasic acid quality 1-3%.
Specifically, above-mentioned titanate coupling agent NDZ-201 viscosity is 1200mm2/ s, pH value 8.0, above-mentioned three isopropyl Aluminium content is 13.5% in epoxide aluminium.
Technical scheme more than, the beneficial effects of the invention are as follows:
A kind of preparation method of tent bonding PUR provided by the invention, simple to operate, cost is cheap, obtained hot melt Glue, cohesive force is strong, and especially it has excellent weatherability, and for tent during use, glue is not susceptible to showing for failure As effectively extending the service life of tent.Step(1)In, the moisture in dimeric dibasic acid is thoroughly removed, can effectively be lifted poly- Close the speed of reaction and the yield of product;After with dimeric dibasic acid polymerisation occurs for IPD, the polymer of generation, side chain With excellent stability, the phenomenon that main chain is broken can be effectively avoided, and then improves the water resistance, heat-resisting of PUR Become performance, in outdoor application, excellent cohesive force can be kept for a long time, greatly extend the service life of tent;Step Suddenly(2)After sodium phytate and hmds synergy, the content of moisture in reaction system on the one hand can be reduced, on the other hand Sodium phytate can effectively increase the number of hydrogen bond in obtained polymerize, and then effectively improve the toughness after glue dries, and six The silicon amine of methyl two to a certain extent add the mean molecule quantity of polymer, and then improve the weatherability of PUR;Titanium Acid esters coupling agent NDZ-201, aluminium isopropoxide add in final stage, can effectively avoid PUR during storage The phenomenon of coagulation occurs.
Embodiment
In order to make the purpose , technical scheme and advantage of the present invention be clearer, following examples are carried out to the present invention It is further described.It should be appreciated that specific embodiment party example described herein is not used to limit only to explain the present invention The fixed present invention.
Embodiment 1
A kind of preparation method of tent bonding PUR, including following operating procedure:
(1)By dimeric dibasic acid and benzene according to 10:After 3 ratio mixing, fluidized state is heated under normal pressure, keeps fluidized state 8min Afterwards, room temperature is cooled to, is 1 according to mass volume ratio:300 ratio adds anhydrous magnesium sulfate thereto, is evaporated under reduced pressure, and nothing is made Water dimeric dibasic acid;
(2)By weight, by 54 parts of steps(1)The anhydrous dimeric dibasic acid of gained, 34 parts of caprolactams, 10 parts of IPDs Add into autoclave, and continue to add 2 parts of sodium phytates, 4 parts of hmds, 0.1 part of concentrated sulfuric acid thereto, be well mixed Afterwards, the temperature of autoclave is risen to 230 DEG C, it is that 1.3MPa reacts 160min to keep pressure;
(3)After pressure release, after being cooled to 120 DEG C, titanate coupling agent NDZ-201, aluminium isopropoxide are added thereto, mixing is equal After even, after insulation reaction 60min, mixture is down to room temperature, finished product.
Specifically, in above-mentioned dimeric dibasic acid, mono-acid content is 4%, dimer content 88%, and tripolymer content is 8%, relatively Molecular mass is 570.
Specifically, above-mentioned steps(3)In, titanate coupling agent NDZ-201 addition is step(2)In anhydrous dimeric dibasic acid The 3% of quality, the addition of aluminium isopropoxide is step(2)In anhydrous dimeric dibasic acid quality 1%.
Specifically, above-mentioned titanate coupling agent NDZ-201 viscosity is 1200mm2/ s, pH value 8.0, above-mentioned three isopropyl Aluminium content is 13.5% in epoxide aluminium.
Embodiment 2
A kind of preparation method of tent bonding PUR, including following operating procedure:
(1)By dimeric dibasic acid and benzene according to 13:After 3 ratio mixing, fluidized state is heated under normal pressure, keeps fluidized state After 10min, room temperature is cooled to, is 1 according to mass volume ratio:300 ratio adds anhydrous magnesium sulfate thereto, is evaporated under reduced pressure, Anhydrous dimeric dibasic acid is made;
(2)By weight, by 60 parts of steps(1)The anhydrous dimeric dibasic acid of gained, 36 parts of caprolactams, 13 parts of IPDs Add into autoclave, and continue to add 3 parts of sodium phytates, 6 parts of hmds, 0.2 part of concentrated sulfuric acid thereto, be well mixed Afterwards, the temperature of autoclave is risen to 235 DEG C, it is that 1.4MPa reacts 180min to keep pressure;
(3)After pressure release, after being cooled to 130 DEG C, titanate coupling agent NDZ-201, aluminium isopropoxide are added thereto, mixing is equal After even, after insulation reaction 70min, mixture is down to room temperature, finished product.
Specifically, in above-mentioned dimeric dibasic acid, mono-acid content is 4%, dimer content 88%, and tripolymer content is 8%, relatively Molecular mass is 570.
Specifically, above-mentioned steps(3)In, titanate coupling agent NDZ-201 addition is step(2)In anhydrous dimeric dibasic acid The 5% of quality, the addition of aluminium isopropoxide is step(2)In anhydrous dimeric dibasic acid quality 2%.
Specifically, above-mentioned titanate coupling agent NDZ-201 viscosity is 1200mm2/ s, pH value 8.0, above-mentioned three isopropyl Aluminium content is 13.5% in epoxide aluminium.
Embodiment 3
A kind of preparation method of tent bonding PUR, including following operating procedure:
(1)By dimeric dibasic acid and benzene according to 15:After 3 ratio mixing, fluidized state is heated under normal pressure, keeps fluidized state After 12min, room temperature is cooled to, is 1 according to mass volume ratio:300 ratio adds anhydrous magnesium sulfate thereto, is evaporated under reduced pressure, Anhydrous dimeric dibasic acid is made;
(2)By weight, by 65 parts of steps(1)The anhydrous dimeric dibasic acid of gained, 38 parts of caprolactams, 15 parts of IPDs Add into autoclave, and continue to add 4 parts of sodium phytates, 8 parts of hmds, 0.3 part of concentrated sulfuric acid thereto, be well mixed Afterwards, the temperature of autoclave is risen to 240 DEG C, it is that 1.5MPa reacts 200min to keep pressure;
(3)After pressure release, after being cooled to 140 DEG C, titanate coupling agent NDZ-201, aluminium isopropoxide are added thereto, mixing is equal After even, after insulation reaction 80min, mixture is down to room temperature, finished product.
Specifically, in above-mentioned dimeric dibasic acid, mono-acid content is 4%, dimer content 88%, and tripolymer content is 8%, relatively Molecular mass is 570.
Specifically, above-mentioned steps(3)In, titanate coupling agent NDZ-201 addition is step(2)In anhydrous dimeric dibasic acid The 6% of quality, the addition of aluminium isopropoxide is step(2)In anhydrous dimeric dibasic acid quality 3%.
Specifically, above-mentioned titanate coupling agent NDZ-201 viscosity is 1200mm2/ s, pH value 8.0, above-mentioned three isopropyl Aluminium content is 13.5% in epoxide aluminium.
PUR is made in the method provided respectively with each embodiment, commercially available common heat seeling coating glue is chosen, then by it It is respectively coated the TPU cloth in formed objects(10cm×10cm)On, sample is placed and deposited 30 in an outdoor environment, tests it Peel strength, test result are as shown in table 1:
The PUR weatherability of table 1 is tested
Project Peel strength at 1 day, N/cm Peel strength at 30 days, N/cm
Embodiment 1 73 68
Embodiment 2 75 70
Embodiment 3 76 73
Comparative example 66 34
As shown in Table 1, PUR produced by the present invention, there is excellent weatherability and adhesion strength.
Certainly, it is limitation of the present invention that described above, which is not, and the present invention is also not limited to the example above, the art Those of ordinary skill, the present invention essential scope in, change, change, addition or the replacement made, should all belong to the present invention Protection domain.

Claims (4)

1. a kind of preparation method of tent bonding PUR, it is characterised in that including following operating procedure:
(1)By dimeric dibasic acid and benzene according to 10-15:After 3 ratio mixing, fluidized state is heated under normal pressure, keeps fluidized state After 8-12min, room temperature is cooled to, is 1 according to mass volume ratio:300 ratio adds anhydrous magnesium sulfate thereto, and decompression is steamed Evaporate, anhydrous dimeric dibasic acid is made;
(2)By weight, by 54-65 part steps(1)The anhydrous dimeric dibasic acid of gained, 34-38 parts caprolactam, 10-15 parts are different Isophoronediamine is added into autoclave, and continues to add 2-4 parts sodium phytate, 4-8 parts hmds, 0.1- thereto 0.3 part of concentrated sulfuric acid, after being well mixed, the temperature of autoclave is risen to 230-240 DEG C, keeps pressure to be reacted for 1.3-1.5MPa 160-200min;
(3)After pressure release, after being cooled to 120-140 DEG C, titanate coupling agent NDZ-201, aluminium isopropoxide are added thereto, is mixed After closing uniformly, after insulation reaction 60-80min, mixture is down to room temperature, finished product.
2. according to a kind of preparation method of tent PUR described in claim 1, it is characterised in that above-mentioned dimeric dibasic acid In, mono-acid content is 4%, dimer content 88%, and tripolymer content is 8%, relative molecular mass 570.
3. according to a kind of preparation method of tent PUR described in claim 1, it is characterised in that above-mentioned steps(3) In, titanate coupling agent NDZ-201 addition is step(2)In anhydrous dimeric dibasic acid quality 3-6%, aluminium isopropoxide Addition is step(2)In anhydrous dimeric dibasic acid quality 1-3%.
4. according to a kind of preparation method of tent PUR described in claim 3, it is characterised in that above-mentioned titanate esters are even The viscosity for joining agent NDZ-201 is 1200mm2/ s, pH value 8.0, aluminium content is 13.5% in above-mentioned aluminium isopropoxide.
CN201710902601.5A 2017-09-29 2017-09-29 A kind of preparation method of tent PUR Pending CN107603556A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710902601.5A CN107603556A (en) 2017-09-29 2017-09-29 A kind of preparation method of tent PUR

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710902601.5A CN107603556A (en) 2017-09-29 2017-09-29 A kind of preparation method of tent PUR

Publications (1)

Publication Number Publication Date
CN107603556A true CN107603556A (en) 2018-01-19

Family

ID=61059388

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710902601.5A Pending CN107603556A (en) 2017-09-29 2017-09-29 A kind of preparation method of tent PUR

Country Status (1)

Country Link
CN (1) CN107603556A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103113843A (en) * 2013-02-20 2013-05-22 江苏永林油脂化工有限公司 Preparation method of low-acid-value low-viscosity dimer acid type polyamide hot melt adhesive
CN103468198A (en) * 2013-09-17 2013-12-25 上海天洋热熔胶有限公司 Preparation method of dimer acid type polyamide hot melt adhesive for heat-shrinkable sleeve
CN103484053A (en) * 2013-10-16 2014-01-01 上海天洋热熔胶有限公司 Preparation method of hot-melt adhesive for conductive fabrics
CN104356999A (en) * 2014-10-22 2015-02-18 重庆市旭星化工有限公司 Copolyamide hot melt adhesive

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103113843A (en) * 2013-02-20 2013-05-22 江苏永林油脂化工有限公司 Preparation method of low-acid-value low-viscosity dimer acid type polyamide hot melt adhesive
CN103468198A (en) * 2013-09-17 2013-12-25 上海天洋热熔胶有限公司 Preparation method of dimer acid type polyamide hot melt adhesive for heat-shrinkable sleeve
CN103484053A (en) * 2013-10-16 2014-01-01 上海天洋热熔胶有限公司 Preparation method of hot-melt adhesive for conductive fabrics
CN104356999A (en) * 2014-10-22 2015-02-18 重庆市旭星化工有限公司 Copolyamide hot melt adhesive

Similar Documents

Publication Publication Date Title
EP3027668B2 (en) Polyurethane adhesive film
WO2017088765A1 (en) Method for preparing modified wet-cured polyurethane hot melt adhesive
CN107987759A (en) A kind of aluminum-plastic membrane used for packaging lithium battery corrosion resistant type adhesive
WO2016090777A1 (en) Tpu composite material for oil storage bag
CN107722917A (en) A kind of preparation method of solvent-free dual-component polyurethane boiling adhesive
JP2950057B2 (en) Adhesive composition
CN105111399A (en) Water pressure resistant water-based polyurethane resin
CN105440244A (en) High-film-forming-property aqueous polyurethane resin as well as preparation method and use method of high-film-forming-property aqueous polyurethane resin
CN104231879A (en) Water-based polyester primer for enhancing printing and aluminum plating and preparation method of water-based polyester primer
CN103254399A (en) High-water-pressure-resistant cold-resistant polyurethane resin and preparation method thereof
CN107603556A (en) A kind of preparation method of tent PUR
CN105097971A (en) Solar cell backboard
JP2004010655A (en) Two-package curable polyurethane resin composition and gas barrier laminating adhesive
CN106833486A (en) A kind of efficient bi-component polyurethane adhesive composition for VMPET/PE structures and preparation method thereof
CN106367015A (en) Water-proof high-strength adhesive and preparation method thereof
CN101392164B (en) Environment-friendly type high performance water vacuum plastics-absorption adhesive
CN101818038A (en) Method for preparing film adhesive for aluminum honeycomb panel sandwich structure
CN106366968A (en) Anticorrosive adhesive tape and preparation method thereof
CN106008988A (en) Preparation method of polypropylene-based modified polyurethane composite material
CN106117492A (en) A kind of preparation method of organosilicon/epoxy resin modification polyurethane
JPH1161083A (en) Two-component curable laminating adhesive and production of laminated film by using same
CN109439265B (en) Production method of functional multipurpose double-component polyurethane adhesive
TWI710616B (en) Solvent-free polyurethane adhesive and dual-coating solvent-free polyurethane adhesive
CN109177391B (en) Special waterproof and gas-insulating film for refrigeration house construction industry and preparation method and installation method thereof
US3692742A (en) Water resistant polyurethane/polymer laminate

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20180119