CN103044670A - Polyether ester for adhesion of textile adhesive - Google Patents
Polyether ester for adhesion of textile adhesive Download PDFInfo
- Publication number
- CN103044670A CN103044670A CN2011103884833A CN201110388483A CN103044670A CN 103044670 A CN103044670 A CN 103044670A CN 2011103884833 A CN2011103884833 A CN 2011103884833A CN 201110388483 A CN201110388483 A CN 201110388483A CN 103044670 A CN103044670 A CN 103044670A
- Authority
- CN
- China
- Prior art keywords
- polyether ester
- bonding
- terephthalic acid
- textiles
- textile adhesive
- 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
Links
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
The invention discloses a polyether ester for the adhesion of a textile adhesive, aiming to solve the problem that a material which is more sensitive to the temperature in the traditional polyether ester for the textile adhesive is easy to be damaged. The polyether ester comprises terephthalic acid, isophthalic acid, 1,4-butanediol and polyethylene glycol, wherein the molar ratio of the terephthalic acid to the isophthalic acid is 40-45:60-50, and the mass of the polyethylene glycol is 10.5-25 percent of the total mass of the polyether ester. With the adoption of the polyether ester for the textile adhesive, when being processed and ground, the polyether ester is not easy to be damaged; and meanwhile, a melting point of the polyether ester descends, and the polyether ester is more convenient to be used.
Description
Technical field
The present invention relates to a kind of for the bonding polyether ester of bonding of textiles agent.
Background technology
At present, existing people disclosed many different copolyesters that are used as textiles hot pressed powder polymkeric substance.Only containing in the group situation of low molecular weight dicarboxylic acids and dibasic alcohol, this kind polyester is stable not for the effect that resembles used organic solvent of textiles when dry-cleaning.This kind polyester is used for the common textiles that only washes with water mostly, for example is used to increase very collar, cuff and blouse.In order to obtain to bear the bonding of textiles that washing also can stand to dry-clean, once the someone delivered the application that reaches a standard in the block copolymerization polyether ester.For example JP-A54-153835 discloses a kind of polyether ester as the spun bonded agent, it comprises a) terephthalic acid group, the b of 70~40% (moles)) 30~60% (mole) m-phthalic acid group, c) 1,4-butyleneglycol group, and d) (a) to d) gross weight) 1~10% a kind of polyalkylene ether glycols group, the molar mass of this polyalkylene ether glycols group is 0.3~6kg/mol, all components all in all polycondensation combine; Component d) comprises polyoxyethylene glycol, although poly-BDO is better.Because component d) content lower, so the melt viscosity of this polyester is higher, to produces the higher underground heat of the bonding needs of tackiness agent-pressures temperature and/or grow and press (subsides) and close time or elevated pressures.Therefore, thisly in this course of processing, may sustain damage under the certain environment than more sensitive material to temperature.
Summary of the invention
Goal of the invention of the present invention is: for the present existing problem that temperature is sustained damage easily than more sensitive material for the polyether ester of bonding of textiles agent, provide a kind of for the bonding polyether ester of bonding of textiles agent, product of the present invention is when processing and grinding, not fragile, its melting point depression is more easy to use simultaneously.
To achieve these goals, the present invention adopts following technical scheme:.
A kind of for the bonding polyether ester of bonding of textiles agent, comprise terephthalic acid, m-phthalic acid, 1,4-butyleneglycol and polyoxyethylene glycol, the mol ratio of described terephthalic acid and m-phthalic acid are 40~45:60~50, and the quality of described polyoxyethylene glycol is 10.5~25% of above-mentioned polyether ester total mass.
The mol ratio of described terephthalic acid and m-phthalic acid is 42: 58 or 45: 55.
The BDO of 1%-20%mol replaces with hexylene glycol.
The BDO of 5~10%mol replaces with hexylene glycol.
The polyoxyethylene glycol of 5%-10%wt is with two or triglycol, and perhaps lower molecular weight alkylene ether glycol replaces.
Applicant of the present invention finds, have product that a high proportion of like this m-phthalic acid and polyoxyethylene glycol consist of unexpectedly can be processed with grinding and no problem, with regard to the knowledge of now having grasped, this is seemingly impossible.And, also found melting point depression almost 20 ℃ (DSC (differential scanning calorimetry): 103~108 ℃), thus more easy to use.It far is high bounding force to important cladding material with above-mentioned also being of combining.However, also may greatly reduce the back side is clamminess.
As required, the additive as grinding aid such as nucleator (for example micronization talcum), static inhibitor, lubricant or wax can also directly be added or adding in the polyether ester process of lapping or after this process in the polyether ester melt.
Embodiment
Disclosed all features in this specification sheets, or the step in disclosed all methods or the process except mutually exclusive feature and/or step, all can make up by any way.
Disclosed arbitrary feature in this specification sheets (comprising any accessory claim, summary) is unless special narration all can be replaced by other equivalences or the alternative features with similar purpose.That is, unless special narration, each feature is an example in a series of equivalences or the similar characteristics.
Embodiment 1
Polyether ester is comprised of following component: the polyoxyethylene glycol of whole component total masses 11% in 42% (mole) terephthalic acid, 58% (mole) m-phthalic acid, 100% (mole) BDO and the polyester.
Embodiment 2
Polyether ester is comprised of following component: the polyoxyethylene glycol of whole component total masses 11% in 45% (mole) terephthalic acid, 55% (mole) m-phthalic acid, 100% (mole) BDO and the polyester.
Reference examples (DE-C3132059)
Reference examples is comprised of following component: the polyoxyethylene glycol of whole component total masses 11% in 50% (mole) terephthalic acid, 50% (mole) m-phthalic acid, 100% (mole) BDO and the polyester.
Described polyether ester is by traditional melt polycondensation method preparation.
Simultaneous test
This copolyester is mixed with a kind of traditional pasty state base-material and be coated on a 20g/m by 25 purpose wire mark stencils
2The conventional nylon non-woven fabrics above, drying is clinkering again.Then non-woven fabrics is adhered on two kinds of cladding materials that are selected from the second following table and also measure subsequently bounding force.
The pasty state base-material:
Water 1800g
MiroxHP 40g
Intrasol12/18/5 60g
Tegopren5847 10g
Unimoll66 80g
VestameltX1151-P1 600g
MiroxOX 100g
Experimental result is as shown in table 1.
Table 1 test-results
The PEG4000=molecular weight is 4000 polyoxyethylene glycol
The open time of OT=
Table 2 has provided the washing test data.
Table 2 washing test data
Test | Example 1 | Example 2 | Comparative Examples |
Roll banding | 1.75N/5cm | 0.1N/5cm | 5N/5cm |
Be clamminess in the back side | 1.5N/10cm | 0.5N/10cm | 4N/10cm |
Separating force: (wash sticking georgette) first dry-cleaning after | 4 6 | 3 6 | 3 4 |
Separating force: first after (cotton poplin) 40 ℃ of washings | 8 8 | 8 9.5 | 4 4.5 |
Bond condition:
120 ℃ of bounding point temperature
10 seconds bonding time
3.5 newton exert pressure
Enforcement 1-2 of the present invention all is better than Comparative Examples in all respects, and wherein the water-fast scourability of embodiment 2 is particularly outstanding.
The present invention is not limited to aforesaid embodiment.The present invention expands to any new feature or any new combination that discloses in this manual, and the arbitrary new method that discloses or step or any new combination of process.
Claims (5)
1. one kind is used for the bonding polyether ester of bonding of textiles agent, comprise terephthalic acid, m-phthalic acid, 1,4-butyleneglycol and polyoxyethylene glycol, the mol ratio of described terephthalic acid and m-phthalic acid are 40~45:60~50, and the quality of described polyoxyethylene glycol is 10.5~25% of above-mentioned polyether ester total mass.
2. according to claim 1ly it is characterized in that for the bonding polyether ester of bonding of textiles agent the mol ratio of described terephthalic acid and m-phthalic acid is 42: 58 or 45: 55.
3. according to claim 1 for the bonding polyether ester of bonding of textiles agent, it is characterized in that: the BDO of 1%-20%mol replaces with hexylene glycol.
According to claimed in claim 1 for the bonding polyether ester of bonding of textiles agent, it is characterized in that: the BDO of 5~10%mol replaces with hexylene glycol.
According to claimed in claim 1 for the bonding polyether ester of bonding of textiles agent, it is characterized in that: the polyoxyethylene glycol of 5%-10%wt is with two or triglycol, and perhaps lower molecular weight alkylene ether glycol replaces.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2011103884833A CN103044670A (en) | 2011-11-30 | 2011-11-30 | Polyether ester for adhesion of textile adhesive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2011103884833A CN103044670A (en) | 2011-11-30 | 2011-11-30 | Polyether ester for adhesion of textile adhesive |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103044670A true CN103044670A (en) | 2013-04-17 |
Family
ID=48057546
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2011103884833A Pending CN103044670A (en) | 2011-11-30 | 2011-11-30 | Polyether ester for adhesion of textile adhesive |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103044670A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1134947A (en) * | 1995-03-22 | 1996-11-06 | 希尔斯股份公司 | Polyester for bonding of textiles |
-
2011
- 2011-11-30 CN CN2011103884833A patent/CN103044670A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1134947A (en) * | 1995-03-22 | 1996-11-06 | 希尔斯股份公司 | Polyester for bonding of textiles |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1070510C (en) | Polyester for bonding of textiles | |
TWI608068B (en) | Double-sided adhesive tape | |
CN107001874B (en) | Bonding sheet | |
CN101240060B (en) | Crystalline copolyesters having good solubility in unhalogenated solvents and their use | |
US10696880B2 (en) | Polyester adhesive composition and adhesive sheet | |
CN104387548B (en) | A kind of mirror face synthetic leather non-yellow stain polyurethane resin and preparation method thereof | |
CN102597151B (en) | Pressure-sensitive adhesive composition | |
CN104114661B (en) | Binder composition and adhesive sheet | |
TWI608067B (en) | Adhesive layer, adhesive tape and double-sided adhesive tape | |
KR101578233B1 (en) | Bonding of heat-activated films including a plasticizer | |
CN101613586A (en) | A kind of reaction type polyurethane hot-melt adhesive and preparation method thereof | |
CN106674508A (en) | Preparation method of pure water-soluble antimony-free modified polyester | |
CN112898914A (en) | Method for producing surface-protecting pressure-sensitive adhesive sheet | |
JP5980674B2 (en) | Polyester pressure-sensitive adhesive composition and pressure-sensitive adhesive sheet using the pressure-sensitive adhesive composition | |
CA1145893A (en) | Copolyester adhesives | |
CN103044670A (en) | Polyether ester for adhesion of textile adhesive | |
US6410627B1 (en) | Use of high hydroxyl compounds for water sensitive hot melt adhesives | |
US3717528A (en) | Fabric bonding with thermoplastic fibrous mats | |
TW201718697A (en) | Polyester resin, method for producing polyester resin, resin composition, resin-clad fabric, and method for producing resin-clad fabric | |
JP3165398B2 (en) | Copolyetherester hot melt material and method of using the same | |
JP4585152B2 (en) | Biodegradable laminate | |
CN108728035A (en) | A kind of self-catalysis type polyurethane hot melt adhesive and preparation method thereof | |
JPS6335187B2 (en) | ||
CN103289628B (en) | Polyethylene hot melt adhesive used for sheet materials and preparation method thereof | |
CN106634721B (en) | Acrylic ester aquosity hot melt latex solution of adhesion lining cloth and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20130417 |