CN1415685A - Method for controlling the melt index of polyamide hot-melt adhesive - Google Patents
Method for controlling the melt index of polyamide hot-melt adhesive Download PDFInfo
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- CN1415685A CN1415685A CN 01133360 CN01133360A CN1415685A CN 1415685 A CN1415685 A CN 1415685A CN 01133360 CN01133360 CN 01133360 CN 01133360 A CN01133360 A CN 01133360A CN 1415685 A CN1415685 A CN 1415685A
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- polycondensation
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Abstract
A method for controlling the fusion index of the hot-melt polyamide adhesive features that according to the input current variation of stirring motor, the fusing polycondensation step in its synthesizing process is controlled. Its advantages are high correctness and high adhesion strength.
Description
1, technical field
The present invention relates to the preparation of polyamide hot, particularly a kind of method of controlling polyamide thermosol for clothing melting index in the melt phase polycondensation process.
2, background technology
Polyamide hot (PA) is a kind of hot melt adhesive that copolycondensations such as multiple aliphaticdicarboxylic acid and aliphatic diamine obtain, be mainly used in the production of clothes hot melt lining cloth, the hot melt lining cloth of clothes plays effects such as skeleton reinforcement, typing to clothes, be the requisite auxiliary material of garment production.Stripping strength is a bonding fastness between garment material and the fusible interlining, it is the very important use propertieies of clothes with hot melt adhesive, that clothes not only require is well-pressed, flexible, do not walk type, dress is beautiful and comfortable but also to require be water-fast washing and anti-dry-cleaning, washing back clothes are not walked type, have only in this way just improved the clothes class.The employed hot melt adhesive washing fastness of the washing fastness of clothes and clothes fusible interlining (washing stripping strength) has direct relation.For polyamide thermosol for clothing, the stripping strength of hot melt adhesive (comprising washing, dry-cleaning stripping strength) is except outside the Pass having with the prescription composition of hot melt adhesive and the determined fusing point of composition of filling a prescription, and also the polymerization degree with hot melt adhesive has much relations.The polymerized unit that the preparation polyamide hot generally uses is nylon 6, nylon 1010, nylon 12, nylon 613, nylon 1212 etc., with the polycondensate more than three kinds or three kinds wherein.If determined the prescription and the composition of polyamide hot, the fusion range of hot melt adhesive is just basic have been determined, the stripping strength of polyamide hot depends primarily on (comprising washing, dry-cleaning stripping strength) polymerization degree of hot melt adhesive so.Use has the hot melt adhesive of the suitable polymerization degree and makes the clothes fusible interlining, in pressing the process of scalding, hot melt adhesive promptly not exclusively is penetrated in lining cloth and the lining, can not between lining cloth and lining, form independently film again, the polymerization degree of polyamide thermosol for clothing just can make to have higher bonding fastness between clothes and the lining cloth, so must be controlled within the specific limits.The height of the hot melt adhesive polymerization degree is relevant with the melt viscosity of hot melt adhesive, and the melt viscosity of hot melt adhesive can be represented with the melting index of hot melt adhesive, therefore the size of melting index can be represented the height of the hot melt adhesive polymerization degree, and promptly melting index is big more, and the polymerization degree is more little.So in the building-up process of polyamide hot, need melting index is controlled, make hot melt adhesive have the suitable polymerization degree.
In the melt phase polycondensation process of polyamide hot, in order to control the melting index of hot melt adhesive, generally the method for Cai Yonging is to add molecular weight regulator in thermosol formula, and the control polycondensation reaction time reaches the purpose of control melting index.Adopted the method that adds molecular weight regulator as Japanese Patent JP 57-12079, molecular weight regulator is acetate or phenylformic acid etc., synthesis under normal pressure 1 hour again after the pressurization polycondensation finishes.U.S. Pat 4,045,389 have adopted with monocarboxylic acid as molecular weight regulator, control the method for normal pressure polycondensation reaction time again.Because being used for the various raw materials of synthetic hot melt adhesive may change at any time, wherein the small amount of impurities of Cun Zaiing can produce very big influence to polycondensation process, so exist certain defective by adding the method that quantitative molecular weight regulator and control polycondensation reaction time control the hot melt adhesive melting index, the melting index fluctuation of synthetic hot melt adhesive is bigger, thereby influence the use properties of hot melt adhesive, especially the stripping strength to hot melt adhesive has bigger influence.In case raw material changes or needs to change melting index, can only determine the add-on and the polycondensation reaction time of molecular weight regulator by doing experiment again.In order to address this problem U.S. Pat 4,390,667 methods that adopt are to prepare the polyamide hot of high fusion index earlier, by adding phosphate compound, regulate melt index of polyamide hot-melt adhesive and viscosity, then until reaching required numerical value.Chinese patent CN 1070660A adopts the method that adds entry to make polyamide hot meet the requirements of melt viscosity.Though more than two kinds of methods can both make the melting index of hot melt adhesive have suitable value, but owing to the stripping strength that affiliation reduces polyamide hot greatly that adds of other material, so all be not the control method of the melting index of ideal polyamide thermosol for clothing.Chinese patent CN 1074916A has adopted in polyamide hot melt polycondensation reaction process, is delivered to the method that moment of torsion on the agitator is estimated polymer viscosity by observation.This method can only be estimated the viscosity (polymerization degree or melting index) of polymkeric substance by rule of thumb, can not read the accurate numerical value of melting index.
3, summary of the invention
The objective of the invention is to overcome the deficiency that prior art exists, propose a kind of in the preparation process of polyamide hot, the method of control melt index of polyamide hot-melt adhesive, this method is accurately convenient, the hot melt adhesive that polycondensation is obtained has the ideal melting index, has guaranteed that hot melt adhesive has higher bonding strength in use.
The present invention is according to the variation of agitator motor received current, and the melt phase polycondensation process was controlled when polyamide hot was synthesized, so that reach the purpose of required melting index, its method mainly comprises:
A. determine preparation needed reaction raw materials of polyamide hot and consumption thereof.Described reaction raw materials can be gone up any suitable raw material, generally can be selected from nylon 6, nylon 66, NYLON610, nylon 1010, nylon 12, nylon 613, the nylon 1212 more than three kinds or three kinds.These raw materials generally are the nylon polymers that monomer, aliphaticdicarboxylic acid and aliphatic diamine synthetic nylon salt, the aliphaticdicarboxylic acid of aliphaticdicarboxylic acid and aliphatic diamine becomes with the aliphatic diamine polycondensation.In addition, when the preparation polyamide hot, generally also can select to use molecular weight regulator and polymerization starter etc., according to concrete needs, also can select to use oxidation inhibitor, sanitas, static inhibitor, lubricant etc. sometimes.Molecular weight regulator comprises monocarboxylic acid, monoamine, and its consumption generally accounts for the 0.05w%～5w% of diprotic acid or diamine total amount, and monocarboxylic acid or monoamine are preferably C
2～C
18Straight chain fatty acid or aliphatic amide.Polymerization starter is preferably water, and add-on is 5w%～35w%, is preferably 10w%～20w%.
B. according to determined each reaction raw materials of step a and consumption thereof, required each reaction raw materials joined in proportion carry out polycondensation in the batch condensation polymerization reactor, be heated to and begin when reactor temperature is 60～150 ℃ to stir, begin when preferably reactor temperature is 80～120 ℃ to stir.When reaching more than 200 ℃, temperature begins polycondensation, keeping temperature of reaction is 200～320 ℃, be preferably 250～280 ℃, keep-uping pressure is 1.5～2.5MPa, is preferably 1.7～2.0Mpa, reaction 0.5～6h, generally be to begin to put pressure behind 1.5～2.5h, pressure is reduced to normal pressure, in 1～2h, pressure can be reduced to normal pressure usually, put the water that the pressure process discharges in the system and polycondensation produces, polycondensation is proceeded.
When c. carrying out melt phase polycondensation first, proceed to the synthesis under normal pressure stage at melt polycondensation reaction, the melting index of sampling and measuring differential responses time response thing is drawn melting index and the corresponding relation curve of agitator motor received current according to measurement result.Generally 5～15min takes a sample once and measures its melting index at interval, and best 8～12min takes a sample once, and number of times at least 2 times that add up to take a sample generally should be not less than 3 times, preferably are not less than 5 times.Certainly the sampling number of times is many more, and the curve of drawing may be accurate more, but operates trouble.
When d. carrying out melt polycondensation reaction again, can be according to the relation curve of melting index of drawing and agitator motor received current, at first find the numerical value of the agitator motor received current corresponding with desired melting index from curve, in view of the above by the numerical value of agitator motor received current in the monitoring melt phase polycondensation process, control the time that polycondensation finishes then.Generally be numerical value when agitator motor received current actual in the melt phase polycondensation process when reaching on the described curve value corresponding, melt polycondensation reaction can finish.
Also can pass through sampling and measuring polymerization ofathe reactants degree or melt viscosity among the above-mentioned steps C, the melting index that replaces the assaying reaction thing, thereby the polymerization degree of drawing or melt viscosity and the corresponding relation curve of agitator motor received current utilize described curve to control the time that polycondensation finishes at above-mentioned d then in the step.
In addition, above-mentioned with also can be in c step according to the data of sampling and measuring, method with mathematical regression, calculate the mathematical model between melting index (or the polymerization degree or melt viscosity) and the agitator motor received current, just can control the time that polycondensation finishes at described d in the step like this according to mathematical model.The data that can certainly utilize c to be determined in the step by modes such as formulation mathematic(al) tables, reach the purpose of described d control control polycondensation concluding time in the step.
The effect of agitator motor is for each reaction raw materials thorough mixing described in the b step of the present invention, so its rotating speed can specifically be determined according to practical situation, carry out work with a constant rotational speed then, like this along with the carrying out that reacts, the character of reactant changes in the reactive system, and the received current of agitator motor also respective change can take place.
In actual mechanical process, can reach purpose of the present invention by the received current of monitoring agitator motor.Also can transfer the size of agitator motor received current to direct demonstration melting index (or the polymerization degree or melt viscosity) by signal output, very intuitively convenient.
The invention has the advantages that:
1. the drafting of melting index (polymerization degree or melt viscosity) and the corresponding curve of agitator motor received current (mathematical model or expression formula or mathematic(al) table) is directly carried out in technological process, need not specially do experiment, and institute fetch data do not need too many.
2. utilize melting index of drawing (polymerization degree or melt viscosity) and the corresponding curve of agitator motor received current, can control the melting index (polymerization degree or melt viscosity) of hot melt adhesive easily, thereby make the synthetic hot melt adhesive have stable performance, can also regulate the melting index (polymerization degree or melt viscosity) of polyamide hot as required arbitrarily, so that satisfy different purposes.
3. the shown numerical value of the indicator gauge of agitator motor received current can transfer direct demonstration melting index (polymerization degree or melt viscosity) to by signal output, and is very intuitively convenient.
4, description of drawings
Fig. 1, Fig. 2, Fig. 3 and Fig. 4 are respectively the relation curves of hot melt adhesive melting index and agitator motor received current in following embodiment 1,2,3 and 5.
5, embodiment
The invention will be further elaborated below in conjunction with drawings and Examples.
Embodiment 1
Hexanolactam 30kg, NYLON610 salt 27kg, nylon 612 salt 43kg, phosphorous acid 0.25kg, lauric acid 1.5kg are joined in the batch condensation polymerization reactor, add 20kg water, be heated to and begin when reactor temperature is 100 ℃ to stir, when temperature in the kettle was 270 ℃, keep-uping pressure was 1.7～2.0MPa, begin to put pressure behind the 2h, 1.5h reaction to normal pressure, is continued in the back, every 10min sampling, when the agitator motor received current reached 61mA, polycondensation promptly came to an end.Hot melt adhesive melting index and agitator motor received current data such as table 1, relation curve is seen Fig. 1.
The relation of table 1 hot melt adhesive melting index and agitator motor received current
| Normal pressure polycondensation reaction time min | ??10 | ??20 | ??30 | ??40 | ??50 | ??60 |
| Motor received current mA melting index (150 ℃, 21.18N) g/10min | ??41 ??27.0 | ??49 ??18.1 | ??55 ??13.0 | ??59 ??10.8 | ??60 ??10.5 | ??61 ??10.0 |
Embodiment 2
Hexanolactam 35kg, nylon 1010 salt 21kg, nylon 1212 salt 44kg, phosphorous acid 0.25kg, lauric acid 1.5kg are joined in the batch condensation polymerization reactor, add 20kg water, be heated to and begin when reactor temperature is 100 ℃ to stir, when temperature in the kettle was 270 ℃, keep-uping pressure was 1.7～2.0MPa, begin to put pressure behind the 2h, 1.5h reaction to normal pressure, is continued in the back, every 10min sampling, when the agitator motor received current reached 58mA, polycondensation promptly came to an end.Hot melt adhesive melting index and agitator motor received current data such as table 2, relation curve is seen Fig. 2.
The relation of table 2 hot melt adhesive melting index and agitator motor received current
| Normal pressure polycondensation reaction time min | ??10 | ??20 | ??30 | ??40 | ????50 | ??55 |
| Motor received current mA melting index (150 ℃, 21.18N) g/10min | ??41 ??28.3 | ??47 ??19.2 | ??51 ??12.8 | ??55 ??11.6 | ????56 ????11.1 | ??58 ??10.0 |
Embodiment 3
Hexanolactam 41kg, hexanediamine 14.7kg, hexanodioic acid 8.6kg, undecane dicarboxylic acid 29kg, phosphorous acid 0.25kg, lauric acid 1.5kg are joined in the batch condensation polymerization reactor, add 20kg water, be heated to and begin when reactor temperature is 100 ℃ to stir, when temperature in the kettle was 270 ℃, keep-uping pressure was 1.7～2.0MPa, begin to put pressure behind the 2h, 1.5h reaction to normal pressure, is continued in the back, every 10min sampling, when the agitator motor received current reached 56mA, polycondensation promptly came to an end.Hot melt adhesive melting index and agitator motor received current data such as table 3, relation curve is seen accompanying drawing 3.
The relation of table 3 hot melt adhesive melting index and agitator motor received current
| Normal pressure polycondensation reaction time min | ??10 | ??20 | ??30 | ????40 | ????50 | ????55 |
| Motor received current mA melting index (150 ℃, 21.18N) g/10min | ??41 ??24.0 | ??47 ??15.5 | ??51 ??11.2 | ????53 ????9.8 | ????54 ????9.3 | ????56 ????9.0 |
With the given prescription of embodiment 2 and form the synthesizing polyamides hot melt adhesive, the melting index that requires hot melt adhesive is to 10.6g/10min, and polycondensation process and operational condition are identical with embodiment 2, and with reference to the accompanying drawings 2, when synthesis under normal pressure when the agitator motor received current reaches 57mA, finish polycondensation.The melting index of measuring the synthetic polyamide hot is that 10.8g/10min conforms to substantially with the melting index 10.6g/10min of requirement.
Hexanolactam 39.4kg, decamethylene diamine 26.6kg, sebacic acid 11.4kg, undecane dicarboxylic acid 23.1kg, phosphorous acid 0.15kg, lauric acid 3.5kg are joined in the batch condensation polymerization reactor, add 20kg water, be heated to and begin when reactor temperature is 100 ℃ to stir, when temperature in the kettle was 260 ℃, keep-uping pressure was 1.7～2.0MPa, 1.5h after begin to put pressure, 1.0h reaction to normal pressure, is continued in the back, every 10min sampling, when the agitator motor received current reached 60mA, polycondensation promptly came to an end.Hot melt adhesive melting index and agitator motor received current data such as table 4, relation curve is seen accompanying drawing 4.
The relation of table 4 hot melt adhesive melting index and agitator motor received current
| Normal pressure polycondensation reaction time min | ??0 | ??10 | ??20 | ??40 | ??50 | ??60 |
| Motor received current mA melting index (160 ℃, 21.18N) g/10min | ??34 ??51.0 | ??42 ??31.2 | ??46 ??24.1 | ??53 ??16.5 | ??55 ??15.3 | ??56 ??15.0 |
Claims (5)
1, the method for control melt index of polyamide hot-melt adhesive comprises:
A. determine preparation needed reaction raw materials of polyamide hot and consumption thereof;
B. according to determined each reaction raw materials of step a and consumption thereof, required each reaction raw materials joined in proportion carry out polycondensation in the batch condensation polymerization reactor, be heated to and begin when reactor temperature is 60～150 ℃ to stir, when reaching more than 200 ℃, temperature begins polycondensation, keeping temperature of reaction is 200～320 ℃, keep-uping pressure is 1.5～2.5MPa, begin to put pressure behind reaction 0.5～6h, pressure is reduced to normal pressure, put the water that the pressure process discharges in the system and polycondensation produces, polycondensation is proceeded;
When c. carrying out melt phase polycondensation first, proceed to the synthesis under normal pressure stage at melt polycondensation reaction, the melting index of sampling and measuring differential responses time response thing is drawn melting index and the corresponding relation curve of agitator motor received current according to measurement result;
When d. carrying out melt polycondensation reaction again, can be according to the relation curve of melting index of drawing and agitator motor received current, at first find the numerical value of the agitator motor received current corresponding with desired melting index from curve, in view of the above by the numerical value of agitator motor received current in the monitoring melt phase polycondensation process, control the time that polycondensation finishes then.
2, according to the method for the described control melt index of polyamide hot-melt adhesive of claim 1, it is characterized in that also can passing through sampling and measuring polymerization ofathe reactants degree or melt viscosity among the described step C, the melting index that replaces the assaying reaction thing, thereby the polymerization degree of drawing or melt viscosity and the corresponding relation curve of agitator motor received current utilize described curve to control the time that polycondensation finishes at above-mentioned d then in the step.
3, according to the method for the described control melt index of polyamide hot-melt adhesive of claim 1, it is characterized in that described c is the data according to sampling and measuring in the step, method with mathematical regression, calculate the mathematical model between melting index and the agitator motor received current, control time that polycondensation finishes according to mathematical model in the step at described d.
4, according to the method for the described control melt index of polyamide hot-melt adhesive of claim 1, it is characterized in that described c utilizes the data that determined, by formulating the mode of mathematic(al) table, reach the purpose of described d control control polycondensation concluding time in the step.
5, according to the method for the described control melt index of polyamide hot-melt adhesive of claim 1, it is characterized in that described C can be with the size of agitator motor received current in the step, transfer direct demonstration melting index to by signal output, thereby reach the purpose that d goes on foot the described control polycondensation concluding time.
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100461044C (en) * | 2006-12-22 | 2009-02-11 | 浙江大学 | Melt index detection fault diagnozing system and method in propylene polymerization production |
| CN100461043C (en) * | 2006-12-22 | 2009-02-11 | 浙江大学 | Melt index detection fault diagnosis system and method for industial polypropylene production |
| CN103709986A (en) * | 2013-12-18 | 2014-04-09 | 苏州市相城区开来化工有限公司 | Polyamide hot melt adhesive |
| CN105524278A (en) * | 2014-09-29 | 2016-04-27 | 中国科学院大连化学物理研究所 | Method for preparing linear macromolecules with controllable molecular weight by solution polycondensation reaction |
| WO2017107859A1 (en) * | 2015-12-21 | 2017-06-29 | 昆山天洋热熔胶有限公司 | Novel hot-melt adhesive and preparation method therefor |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6743273B2 (en) | 2000-09-05 | 2004-06-01 | Donaldson Company, Inc. | Polymer, polymer microfiber, polymer nanofiber and applications including filter structures |
-
2001
- 2001-10-30 CN CNB01133360XA patent/CN1144853C/en not_active Expired - Lifetime
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100461044C (en) * | 2006-12-22 | 2009-02-11 | 浙江大学 | Melt index detection fault diagnozing system and method in propylene polymerization production |
| CN100461043C (en) * | 2006-12-22 | 2009-02-11 | 浙江大学 | Melt index detection fault diagnosis system and method for industial polypropylene production |
| CN103709986A (en) * | 2013-12-18 | 2014-04-09 | 苏州市相城区开来化工有限公司 | Polyamide hot melt adhesive |
| CN103709986B (en) * | 2013-12-18 | 2016-07-06 | 苏州市邦涔高分子科技有限公司 | A kind of polyamide hot |
| CN105524278A (en) * | 2014-09-29 | 2016-04-27 | 中国科学院大连化学物理研究所 | Method for preparing linear macromolecules with controllable molecular weight by solution polycondensation reaction |
| CN105524278B (en) * | 2014-09-29 | 2018-07-20 | 中国科学院大连化学物理研究所 | A kind of method that solution polycondensation reaction prepares the controllable linear polymeric of molecular weight |
| WO2017107859A1 (en) * | 2015-12-21 | 2017-06-29 | 昆山天洋热熔胶有限公司 | Novel hot-melt adhesive and preparation method therefor |
| US10703938B2 (en) | 2015-12-21 | 2020-07-07 | Kunshan Tianyang Hot Melt Adhesive Co., Ltd | Hot-melt adhesive and preparation method therefor |
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