CN1357589A - Multi-purpose polyamide hot melt adhesive and its prepn - Google Patents
Multi-purpose polyamide hot melt adhesive and its prepn Download PDFInfo
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- CN1357589A CN1357589A CN 00132072 CN00132072A CN1357589A CN 1357589 A CN1357589 A CN 1357589A CN 00132072 CN00132072 CN 00132072 CN 00132072 A CN00132072 A CN 00132072A CN 1357589 A CN1357589 A CN 1357589A
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- hot melt
- melt adhesive
- polyamide hot
- described multi
- purpose polyamide
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Abstract
The multi-purpose polyamide hot melt glue consists of two components, A and B. The component A is high molecular weight branched chain polyamide in amorphous structure to provide high strength and high toughness; and the component B is low and middle molecular weight polyamide with microcrystalline structure and has good initial viscosity and flowability and excellent heat resistance. The two components may be combined in any ratio or used alone. The hot melt glue may be used widely in adhering polyolefine, engineering plastic, leather, metal and ceramic in various industries.
Description
The invention belongs to the binding agent field, particularly, the present invention relates to a kind of multi-purpose polyamide hot melt adhesive and preparation method thereof.
Polyamide hot is the very good tackiness agent of a class over-all properties, has been widely used in many industries such as chemical industry, light industry, electronics and automobile.Representational in recent years patent WO9935206A1 (1999), EP1013694A1 (2000), EP911149A2 (1999), EP911151A2 (1999), EP965627A1 (1999), DE19512004A1 (1996), GB231471A1 (1998), US5424371A (1995), CA2117449AA (1995), JP07032529A2 (1995) etc., these patents have been carried out modification to polyamide hot from many aspects, have better heat-resisting and snappiness, can be used for metal, plastics film bonding, but these hot melt adhesives are used for single occasion mostly, and cohesive strength is also not high enough, have only 115N/25mm as the cohesive strength of JP0703529A2 report.Chinese patent CN1215746A is a kind of high strength polyamide hot that is proposed as first contriver by the inventor, its hot stripping strength can reach 300N/25mm, but, hot preferably stripping strength will be a cost to sacrifice initial adhesive strength, therefore execution conditions have been proposed strict demand, range of application has been subjected to certain restriction.
The objective of the invention is provides a kind of multi-purpose polyamide hot melt adhesive and preparation method thereof at the deficiencies in the prior art, be characterized in very large range to adjust easily the composition of polyamide hot, it not only has high bond strength, also has good initial adhesive strength, resistant of high or low temperature is good, softening temperature can be regulated in 95～160 ℃, applicable to heat-shrink tube, and multiple industries such as televisor, automobile, shoemaking, clothing.
The objective of the invention is to realize by following technical measures.
Multi-purpose polyamide hot melt adhesive provided by the invention is by A, B two component polyamide hots combine, A component hot melt adhesive is a high-molecular weight branched chain type polymeric amide, characteristics with high bond strength and high-flexibility, B component hot melt adhesive be in, low-molecular-weight polymeric amide, contain microlitic structure, it is good to have tack, excellent heat resistance, melting range is narrow, advantages such as good fluidity.A, B two component hot melt adhesives can or use separately by the arbitrary proportion combination.
This multi-purpose polyamide hot melt adhesive starting raw material prescription (by mol, band * person is the % of gross weight) is:
Diprotic acid (available dimeracid and HOOC (CH
2)
nCOOH, n=1～11 wherein, or/and
At least a) 0.8～1.2.
Diamine (available H
2N (CH
2)
mNH
2, m=2～13 wherein,
, R=-O-wherein ,-SO
2--CH
2-, R
1=H, Cl is or/and polyoxypropylene diamine is at least a) 1.2～0.8.
Properties-correcting agent (available urea, caprolactam, laurolactam, the omega-amino-undeeanoic acid, nylon salt is or/and nylon 1010 salt is at least a) 0.1～3.0.
Catalyzer
*(phosphoric acid, phosphorous acid is or/and acetate is at least a) 0.05～0.5%.
Thermal oxidation stabilizer
*(available oxidation inhibitor four [β-(3,5-di-t-butyl-4-hydroxymethyl phenyl) propionic acid] pentaerythritol ester, 2, the 6-ditertbutylparacresol, 1,1,3-three-(2-methyl-4-hydroxyl-5-tert-butyl-phenyl) butane, sulfo-two propyl alcohol osmanthus in February esters are or/and calcium-zinc composite stabilizing agent is at least a) 0.5～2.0%.
Filler
*(available white carbon black, lime carbonate is or/and magnesium hydroxide is at least a) 0～50%.
The preparation of multi-purpose polyamide hot melt adhesive
1.A the preparation of component polymeric amide
The preparation of A component polymeric amide is to carry out in the equipment of conventional polymeric amide synthesis method.With etc. mole ratio diprotic acid (wherein the mole ratio of dimeracid account for total dicarboxylic acid 0.8～1.0) and diamine, and properties-correcting agent 0.1～0.5 (mol), catalyzer (weight ratio) 0.05～0.5% adds and has in the autoclave of agitator, thermometer and inert gas gangway, feeds N under oxygen free condition
2Or CO
2Gas; be warming up to 140～200 ℃, the 1.0～2.0MPa that keep-ups pressure reacted 4～6 hours; the venting draining; be evacuated to 1000～1Pa, be warming up to 240～280 ℃, kept 2～6 hours; be cooled to 180 ℃ then; add thermal oxidation stabilizer (weight ratio) 0.5-2%, under nitrogen protection, discharging behind the stirring and evenly mixing.The molecular-weight average of A component polymeric amide has superior bond strengths rendering and good soft flexible, elasticity between 10000～25000.
2.B the preparation of component polymeric amide
The preparation of B component polymeric amide is carried out in conventional polymeric amide synthesis device.Under nitrogen protection; properties-correcting agent such as caprolactam 0.5～3.0 (mol) and catalyzer 0.05～0.5% (weight ratio) adding are earlier had agitator; in the autoclave of thermometer and inert gas gangway; be warming up to 140～180 ℃; reacted 2～4 hours; the polymerization degree of prepolymers such as control caprolactam is 5～30; best 5～15; add then other diprotic acid and diamine (mole ratio is 0.8～1.2: 1.2～0.8); in 160～200 ℃ of temperature, pressure 1.0～1.5MPa reacted 2～6 hours; be evacuated to below the 1000Pa again; be warming up to 220～280 ℃, kept 2～4 hours, be cooled to 200 ℃; add thermal oxidation stabilizer 0.5～2.0% (weight ratio); under nitrogen protection, the discharging that stirs, molecular weight is 6000～15000.The microcell crystalline texture that contains block in the molecular chain of B component hot melt adhesive, when processing temperature reached the microcell fusing, the hot melt adhesive flowability was fine, be full of all spaces between the adherend immediately, when temperature was lower than fusing point, the hot melt adhesive fast setting formed firm tack coat with adherend.
3. the preparation of multi-purpose polyamide hot melt adhesive
Discharging again after A of the present invention, B component polymeric amide can carry out chemical blend in proportion in the aftercondensated stage, also can be in A, B component, carry out the pellet blend respectively after the pelletizing, A, B two components have different constitutional featuress, but consistency is good, A, B component can make up by arbitrary proportion, also can use separately.Also can add filler (as white carbon black, lime carbonate, magnesium hydroxide etc.) during use with reinforcement or reduce cost.
The present invention and CN1215746A relatively have following advantage, it has not only kept very high cohesive strength, and initial adhesive strength and low temperature flexibility are better, particularly water-intake rate reduces by 50%, the tension set regulation range enlarges 180%, the softening temperature regulation range enlarges 260%, thereby has increased considerably use range.
Multi-purpose polyamide hot melt adhesive of the present invention is applicable to the bonding of polyolefin plastics, engineering plastic product, film and the pyrocondensation goods of chemical industry, light industry, communication, electronics and automobile aspect, also can be used for the bonding of leather, metal, pottery and electric elements.
Embodiment
Below by embodiment the present invention is carried out concrete description; be necessary to be pointed out that at this following examples only are used for the present invention is further specified; can not be interpreted as limiting the scope of the invention, the person skilled in the art in this field can make some nonessential improvement and adjustment to the present invention according to the content of the invention described above.
The composition of raw materials of A of the present invention, each embodiment of B component is as shown in table 1.
The method of each embodiment preparation joins in the autoclave that has agitator, thermometer and inert gas gangway for catalyzer, diprotic acid, diamine, the properties-correcting agent that the A component is used, presses the synthetic method of polymeric amide routine, the deoxygenation of finding time, logical N
2Be warming up to 200 ℃, boost to 1.5MPa, reacted 4 hours, the venting dehydration is evacuated to 100Pa, is warming up to 260 ℃, reacts 6 hours, is cooled to 180 ℃ then, adds thermal oxidation stabilizer, and the back that stirs is at N
2The protection bottom discharge.Properties-correcting agent and catalyzer with the B component in raw materials used join earlier in the aforesaid reactor, at N
2Be warming up to 180 ℃ under the protection, make the polymerization degree and be about 10 the polymers that gives, and then add other diprotic acid and diamine; be warming up to 200 ℃; boost to 1.5MPa, reacted 4 hours, venting dewaters; be evacuated to below the 1000Pa; be warming up to 240 ℃, reacted 2 hours, be cooled to 200 ℃ then; add thermal oxidation stabilizer, the back that stirs is at N
2The protection bottom discharge.
As above prepared polyamide hot A (A
1Or A
2) component and B (B
1Or B
2) component, have different constitutional featuress, but consistency is fine.The A component is unformed branched structure, and molecular weight is very high, and intensity, elasticity and flexibility are all fine, and the B component has the block microlitic structure, and in having, lower molecular weight, tack is good, and melting range is narrow.According to different purposes, can rationally utilize the advantage of A, B component, can make up by arbitrary proportion, as shown in table 2, A (A
1Or A
2), B (B
1Or B
2) component also can use separately.
Table 3 is the performance data that embodiment of the invention A, B component are pressed table 2 combination back products obtained therefrom.The result shows that the softening point range of hot melt adhesive of the present invention is easy to regulate in 95～160 ℃ scope, water-intake rate is very low, and snappiness is fine, and elongation at break reaches as high as 1100%, and cold property is good, and doubling is not crisp in the time of-10 ℃.Hot melt adhesive of the present invention melt viscosity in the time of 190 ℃ can be regulated in the scope at 2000～6500mPaS, can be suitable for processing characteristics is required different occasions.The initial adhesive strength of hot melt adhesive of the present invention is also very good, when particularly the B component concentration is more.Hot melt adhesive of the present invention can reach 15MPa to the shearing resistance of Al/Al, can reach 450N/25mm to the stripping strength of PE/PE 60 ℃ the time, be suitable as the structural adhesive of difficult clay soil/polyolefin fully, the electric property of hot melt adhesive of the present invention is also fine, voltage breakdown can reach 25KV/mm, and volume specific resistance is 10
13More than the Ω cm.
Multiple purpose thermosol of the present invention can be allocated as the bonding of the polyolefin plastics, engineering plastic product, film and the pyrocondensation goods that are suitable for chemical industry, light industry, communication, electronics and automobile industry aspect easily, the bonding that also can be used for leather, metal, pottery and electric elements has substantial economics and social benefit.A, B component raw material prescription (by mol, band * person is the % by gross weight) among table 1 embodiment
Table 2 embodiment table 1 component blend product (weight ratio)
The relevant performance of table 3 embodiment table 2 blend product
Claims (9)
1. multi-purpose polyamide hot melt adhesive is characterized in that this hot melt adhesive with the prescription (by mol, being with * number for accounting for the % meter of gross weight) of starting raw material is:
Diprotic acid 0.8～1.2
Diamine 1.2～0.8
Properties-correcting agent 0.1～3.0
Catalyzer * 0.05～0.5%
Thermal oxidation stabilizer * 0.5～2.0%
Filler * 0～50%
2. according to the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that diprotic acid is dimeracid and HOOC (CH
2)
nCOOH, n=1～11 wherein, or
At least a.
3. according to the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that diamine is
H
2N (CH
2)
mNH
2, m=2～13 wherein,
, R=-O-wherein ,-SO
2-,-CH
2-, R
1=H, Cl is or/and polyoxypropylene diamine is at least a.
4. according to the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that properties-correcting agent is urea, caprolactam, laurolactam, omega-amino-undeeanoic acid, nylon salt is or/and nylon 1010 salt is at least a.
5. according to the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that catalyzer is a phosphoric acid, phosphorous acid is or/and acetate is at least a.
6. according to the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that thermal oxidation stabilizer is oxidation inhibitor four [β-(3,5-di-t-butyl-4-hydroxymethyl phenyl) propionic acid] pentaerythritol ester, 2, the 6-ditertbutylparacresol, 1,1,3-three-(2-methyl-4-hydroxyl-5-tert-butyl-phenyl) butane, sulfo-two propyl alcohol osmanthus in February esters are or/and calcium-zinc composite stabilizing agent is at least a.
7. according to the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that filler is white carbon black, lime carbonate is or/and magnesium hydroxide is at least a.
8. according to the preparation method of the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that A component polymeric amide has unformed branched structure, its molecular weight is 10000～25000; B component polymeric amide has microcell crystalline texture, and its molecular weight is 6000～15000.A, B two component compatibilities are good, can the arbitrary proportion combination, also can use separately.
9. according to the purposes of the described multi-purpose polyamide hot melt adhesive of claim 1, it is characterized in that this hot melt adhesive is applicable to the bonding of polyolefin plastics, engineering plastic product, film and the pyrocondensation goods of chemical industry, light industry, communication, electronics and automobile industry aspect, also can be used for the bonding of leather, metal, pottery and electric elements.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB001320726A CN1191316C (en) | 2000-12-12 | 2000-12-12 | Multi-purpose polyamide hot melt adhesive and its prepn |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB001320726A CN1191316C (en) | 2000-12-12 | 2000-12-12 | Multi-purpose polyamide hot melt adhesive and its prepn |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1357589A true CN1357589A (en) | 2002-07-10 |
| CN1191316C CN1191316C (en) | 2005-03-02 |
Family
ID=4594942
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB001320726A Expired - Fee Related CN1191316C (en) | 2000-12-12 | 2000-12-12 | Multi-purpose polyamide hot melt adhesive and its prepn |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1191316C (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1314772C (en) * | 2005-11-11 | 2007-05-09 | 淄博广通化工有限责任公司 | Polyamide hot melt sol preparation method |
| CN101638478B (en) * | 2009-08-26 | 2011-04-13 | 王凡 | Polyamide wax micropowder synthesizing formula and production process thereof |
| CN102492135A (en) * | 2011-11-30 | 2012-06-13 | 上海天洋热熔胶有限公司 | Method for synthesizing dimer acid type polyamide hot melt adhesive |
| CN102653590A (en) * | 2011-03-02 | 2012-09-05 | 骏马化纤股份有限公司 | Polyamide chain extension enhancer and preparation method thereof |
| CN102766413A (en) * | 2012-08-20 | 2012-11-07 | 天津博苑高新材料有限公司 | Integrated circuit (IC) card packaging special hot melting adhesive tape and preparation method thereof |
| CN104356998A (en) * | 2014-09-23 | 2015-02-18 | 苏州雷立特新材料科技有限公司 | Polyamide hot melt adhesive used in electronic packaging field |
| CN106753189A (en) * | 2016-12-30 | 2017-05-31 | 上海天洋热熔粘接材料股份有限公司 | A kind of preparation method of polyamide hot |
| CN110437796A (en) * | 2019-07-18 | 2019-11-12 | 湖南湘铂新材料科技有限公司 | A kind of Wiring harness connector low-pressure injection molding polyamide hot and preparation method thereof |
| CN114656917A (en) * | 2020-12-23 | 2022-06-24 | 上海天洋热熔粘接材料股份有限公司 | Phenol yellowing resistant copolyamide hot melt adhesive and preparation method thereof |
| CN115216263A (en) * | 2022-08-25 | 2022-10-21 | 东莞顺发内衣制造有限公司 | Hot melt adhesive for attaching clothing and cloth and preparation method thereof |
-
2000
- 2000-12-12 CN CNB001320726A patent/CN1191316C/en not_active Expired - Fee Related
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1314772C (en) * | 2005-11-11 | 2007-05-09 | 淄博广通化工有限责任公司 | Polyamide hot melt sol preparation method |
| CN101638478B (en) * | 2009-08-26 | 2011-04-13 | 王凡 | Polyamide wax micropowder synthesizing formula and production process thereof |
| CN102653590A (en) * | 2011-03-02 | 2012-09-05 | 骏马化纤股份有限公司 | Polyamide chain extension enhancer and preparation method thereof |
| CN102492135A (en) * | 2011-11-30 | 2012-06-13 | 上海天洋热熔胶有限公司 | Method for synthesizing dimer acid type polyamide hot melt adhesive |
| CN102766413A (en) * | 2012-08-20 | 2012-11-07 | 天津博苑高新材料有限公司 | Integrated circuit (IC) card packaging special hot melting adhesive tape and preparation method thereof |
| CN102766413B (en) * | 2012-08-20 | 2013-09-18 | 天津博苑高新材料有限公司 | Integrated circuit (IC) card packaging special hot melting adhesive tape and preparation method thereof |
| CN104356998A (en) * | 2014-09-23 | 2015-02-18 | 苏州雷立特新材料科技有限公司 | Polyamide hot melt adhesive used in electronic packaging field |
| CN106753189A (en) * | 2016-12-30 | 2017-05-31 | 上海天洋热熔粘接材料股份有限公司 | A kind of preparation method of polyamide hot |
| CN110437796A (en) * | 2019-07-18 | 2019-11-12 | 湖南湘铂新材料科技有限公司 | A kind of Wiring harness connector low-pressure injection molding polyamide hot and preparation method thereof |
| CN110437796B (en) * | 2019-07-18 | 2021-09-28 | 湖南湘铂新材料科技有限公司 | Low-pressure injection molding polyamide hot melt adhesive for wire harness connector and preparation method thereof |
| CN114656917A (en) * | 2020-12-23 | 2022-06-24 | 上海天洋热熔粘接材料股份有限公司 | Phenol yellowing resistant copolyamide hot melt adhesive and preparation method thereof |
| CN115216263A (en) * | 2022-08-25 | 2022-10-21 | 东莞顺发内衣制造有限公司 | Hot melt adhesive for attaching clothing and cloth and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1191316C (en) | 2005-03-02 |
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