CN101831259A - Adhesive with indicating function - Google Patents

Adhesive with indicating function Download PDF

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Publication number
CN101831259A
CN101831259A CN 201010163539 CN201010163539A CN101831259A CN 101831259 A CN101831259 A CN 101831259A CN 201010163539 CN201010163539 CN 201010163539 CN 201010163539 A CN201010163539 A CN 201010163539A CN 101831259 A CN101831259 A CN 101831259A
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CN
China
Prior art keywords
mixture
add
binding agent
deixis
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.)
Granted
Application number
CN 201010163539
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Chinese (zh)
Other versions
CN101831259B (en
Inventor
宋金萍
张晓婷
王毅
董川
双少敏
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.)
State Grid Corp of China SGCC
Shanxi University
Luliang Power Supply Co of State Grid Shanxi Electric Power Co Ltd
Original Assignee
Shanxi University
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 Shanxi University filed Critical Shanxi University
Priority to CN2010101635390A priority Critical patent/CN101831259B/en
Publication of CN101831259A publication Critical patent/CN101831259A/en
Application granted granted Critical
Publication of CN101831259B publication Critical patent/CN101831259B/en
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Abstract

The invention provides adhesive with indicating function. The adhesive with the indicating function is prepared by heating water to between 40 and 60 DEG C, adding polyvinyl alcohol into the water, heating the mixture till boiling to dissolve the polyvinyl alcohol, cooling the mixture to room temperature, adding sodium carboxymethylcellulose into the mixture, dissolving the sodium carboxymethylcellulose with stirring, continuously heating the mixture to between 40 and 50 DEG C, adding swelling gelatin into the mixture, stirring the mixture uniformly, adding glutaraldehyde into the mixture, stirring the mixture for 10 to 20 minutes, cooling the mixture to room temperature, then adding ethanol solution of triarylmethane leuco dye into the mixture, and adding sodium hydroxide solution into the mixture. The method has the advantages of simple and feasible preparation process, low cost and easy production; and the adhesive has the most prominent characteristics that the color of the adhesive can indicate the adhered part so as to reduce the waste of repeated coating, the color of the adhered part can fade in short time, and no trace is left.

Description

A kind of binding agent with deixis
Technical field
The present invention relates to a kind of Chemical Felter, specifically is a kind of binding agent with deixis.
Background technology
The binding agent of present industrial production is many based on colourless, in use can bring unnecessary waste because of repeatedly smearing.Along with the diversified demand of people to the binding agent color, some enterprise has produced colour adhesive, but used pigment can stay color at the first-class bonded position of paper, can not satisfy people's common requirements.And the allochroic solid of CN101608103A report, though can solve the problem of fading, the main component of binding agent is a polyvinylpyrrolidone, and cost of manufacture is improved greatly.
Summary of the invention
The purpose of this invention is to provide a kind of cost of manufacture lower have binding agent of deixis and preparation method thereof.
A kind of binding agent provided by the invention with deixis, by weight percentage:
Water 65~85
Polyvinyl alcohol 5~15
Xylo-Mucine 4~12
Gelatin 2~8
The glutaraldehyde 0.5~10 of 25-50%
Triaryl methane leuco compound dyestuff 0.1~1
Ethanol 0.5~2
The sodium hydroxide solution 0.04~5 of 2-8%
Essence 0~1.
Described triaryl methane leuco compound dyestuff is thymolphthalein or phenolphthalein; Described essence such as styracin.
Preparation method with binding agent of deixis provided by the invention comprises the steps:
1) take by weighing gelatin, according to the above ratio, with equivalent water logging bubble, swelling is standby;
2), take by weighing triaryl methane leuco compound dyestuff, use dissolve with ethanol, standby;
3), take by weighing other raw material, surplus water is heated to 40-60 ℃, add polyvinyl alcohol, stirring also is warming up to boiling, and it is fully dissolved, and is cooled to room temperature, add Xylo-Mucine, constantly stir and make dissolving fully, continue to be warming up to 40~50 ℃, add step 1) swelling gelatin, stir, add glutaraldehyde, stirred 10-20 minute, be cooled to room temperature, adding step 2) ethanolic soln of prepared triaryl methane leuco compound dyestuff, add sodium hydroxide solution then, stir, promptly get binding agent with deixis.
After adding sodium hydroxide solution, also can add an amount of essence in the described step 3).
Compared with prior art, the present invention has the following advantages:
1, binding agent of the present invention has deixis, can effectively locate and paste the position, reduces excessively in the binding agent use to smear the waste that is brought.
What 2, binding agent presented is blue or red, can take off within a short period of time, and it is residual that the stickup position does not have color.
3, with glutaraldehyde as condensing agent, the condensation ability is obviously improved, also can avoid the harm of using formaldehyde to bring in a large number.
4, the present invention fills a prescription simply, and cost is low, is easy to mass production.
Embodiment
The present invention will be further described below in conjunction with embodiment.
Embodiment 1
1) take by weighing the 1g gelatin, with 1mL water logging bubble, swelling is standby.
2) take by weighing the 0.06g thymolphthalein, use the 0.5mL dissolve with ethanol, standby.
3) in beaker, add 39mL water, be heated to 50 ℃, (polymerization degree is 1700 to add the 3.5g polyvinyl alcohol, alcoholysis degree is 99%), be warming up to boiling, it is fully dissolved, be cooled to room temperature, add 2.5g Xylo-Mucine (viscosity is between the 300-600 centipoise), be warming up to 50 ℃ after the stirring and dissolving, the swelling gelatin that adds the step 1) preparation after the stirring and dissolving, adds the glutaraldehyde of 1mL50%, constantly stir and make it to react 15 minutes, be cooled to room temperature, add step 2) prepared thymolphthalein ethanolic soln, add the sodium hydroxide solution of 0.5mL 5% then, stir, promptly get blue binding agent.
Get the blue binding agent that makes and be applied on the envelope, apply the position and show blueness, with envelope sealing, 5-10 minute color fade sealed bonding firmly.
Embodiment 2
1) take by weighing the 1.5g gelatin, with 1.5mL water logging bubble, swelling is standby.
2) take by weighing the 0.1g thymolphthalein, use the 0.5mL dissolve with ethanol, standby.
3) in beaker, add 40mL water, be heated to 50 ℃, (polymerization degree is 1700 to add the 3g polyvinyl alcohol, alcoholysis degree is 99%), be warming up to boiling, it is fully dissolved, be cooled to room temperature, add 3.5g Xylo-Mucine (viscosity is between the 300-600 centipoise), be warming up to 40 ℃ after the stirring and dissolving, the swelling gelatin that adds the step 1) preparation after the stirring and dissolving, adds the glutaraldehyde of 3mL25%, constantly stir and make it to react 20 minutes, be cooled to room temperature, add step 2) prepared thymolphthalein ethanolic soln, add the sodium hydroxide solution of 1.3mL 3% then, stir, promptly get blue binding agent.
Get the blue binding agent that makes and be applied on the envelope, apply the position and show blueness, with envelope sealing, 5-10 minute color fade sealed bonding firmly.
Embodiment 3
1) take by weighing the 1.5g gelatin, with 1.5mL water logging bubble, swelling is standby.
2) take by weighing 0.1g phenolphthalein, use the 0.5mL dissolve with ethanol, standby.
3) in beaker, add 41mL water, be heated to 50 ℃, (polymerization degree is 1700 to add the 3g polyvinyl alcohol, alcoholysis degree is 99%), be warming up to boiling, it is fully dissolved, be cooled to room temperature, add 3.5g Xylo-Mucine (viscosity is between the 300-600 centipoise), be warming up to 40 ℃ after the stirring and dissolving, add the swelling gelatin of step 1) preparation, after the stirring and dissolving, the glutaraldehyde that adds 2mL50%, constantly stir and make it to react 20 minutes, be cooled to room temperature, add step 2) prepared phenolphthalein ethanolic soln, the sodium hydroxide solution that adds 1.3mL 3% then, add an amount of styracin to savory, stir, promptly get red binding agent.
Get the red binding agent that makes and be applied on the envelope, apply the position and show redness, with envelope sealing, 5-10 minute color fade sealed bonding firmly.

Claims (4)

1. binding agent with deixis is characterized in that components based on weight percentage:
Water 65~85
Polyvinyl alcohol 5~15
Xylo-Mucine 4~12
Gelatin 2~8
The glutaraldehyde 0.5~10 of 25-50%
Triaryl methane leuco compound dyestuff 0.1~1
Ethanol 0.5~2
The sodium hydroxide solution 0.04~5 of 2-8%
Essence 0~1.
2. a kind of binding agent with deixis as claimed in claim 1 is characterized in that, described triaryl methane leuco compound dyestuff is thymolphthalein or phenolphthalein.
3. a kind of preparation method with deixis binding agent as claimed in claim 1 is characterized in that, comprises the steps:
1) take by weighing gelatin, according to the above ratio, with equivalent water logging bubble, swelling is standby;
2), take by weighing triaryl methane leuco compound dyestuff, use dissolve with ethanol, standby;
3), take by weighing other raw material, surplus water is heated to 40-60 ℃, add polyvinyl alcohol, stirring also is warming up to boiling, and it is fully dissolved, and is cooled to room temperature, add Xylo-Mucine, constantly stir and make dissolving fully, continue to be warming up to 40~50 ℃, add step 1) swelling gelatin, stir, add glutaraldehyde, stirred 10-20 minute, be cooled to room temperature, adding step 2) ethanolic soln of prepared triaryl methane leuco compound dyestuff, add sodium hydroxide solution then, stir, promptly get binding agent with deixis.
4. a kind of preparation method with deixis binding agent as claimed in claim 4 is characterized in that, adds an amount of essence in the described step 3) after adding sodium hydroxide solution.
CN2010101635390A 2010-04-30 2010-04-30 Adhesive with indicating function Active CN101831259B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010101635390A CN101831259B (en) 2010-04-30 2010-04-30 Adhesive with indicating function

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010101635390A CN101831259B (en) 2010-04-30 2010-04-30 Adhesive with indicating function

Publications (2)

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CN101831259A true CN101831259A (en) 2010-09-15
CN101831259B CN101831259B (en) 2011-09-07

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102134460A (en) * 2011-02-25 2011-07-27 浙江大学宁波理工学院 Blue solid glue stick with color being changed after application and preparation method thereof
CN102837532A (en) * 2012-09-17 2012-12-26 山西大学 Writing board coated with surface-modified paint and writing liquid matched with writing board
CN103059766A (en) * 2013-01-14 2013-04-24 山西大学 Fading colored solid glue stick and preparation method thereof
CN111500223A (en) * 2020-06-03 2020-08-07 浙江金科胶粘制品有限公司 Glue and preparation process thereof
CN112898951A (en) * 2021-02-02 2021-06-04 山西大同大学 Coal dust suppressant with indication function, preparation method and coal dust suppression method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4954544A (en) * 1989-03-23 1990-09-04 Conros Corporation Modified adhesive composition which undergoes color changes upon application
CN1051748A (en) * 1990-11-14 1991-05-29 广州半导体材料研究所 Colour solid glue
CN1488652A (en) * 2002-07-11 2004-04-14 可乐丽股份有限公司 Vinyl alcohol polymer and method for preparing same
JP2004210883A (en) * 2002-12-27 2004-07-29 Konishi Co Ltd Aqueous adhesive composition
CN101608103A (en) * 2008-06-18 2009-12-23 宁波松鹤文具有限公司 A kind of allochroic solid adhesive and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4954544A (en) * 1989-03-23 1990-09-04 Conros Corporation Modified adhesive composition which undergoes color changes upon application
CN1051748A (en) * 1990-11-14 1991-05-29 广州半导体材料研究所 Colour solid glue
CN1488652A (en) * 2002-07-11 2004-04-14 可乐丽股份有限公司 Vinyl alcohol polymer and method for preparing same
JP2004210883A (en) * 2002-12-27 2004-07-29 Konishi Co Ltd Aqueous adhesive composition
CN101608103A (en) * 2008-06-18 2009-12-23 宁波松鹤文具有限公司 A kind of allochroic solid adhesive and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102134460A (en) * 2011-02-25 2011-07-27 浙江大学宁波理工学院 Blue solid glue stick with color being changed after application and preparation method thereof
CN102837532A (en) * 2012-09-17 2012-12-26 山西大学 Writing board coated with surface-modified paint and writing liquid matched with writing board
CN103059766A (en) * 2013-01-14 2013-04-24 山西大学 Fading colored solid glue stick and preparation method thereof
CN111500223A (en) * 2020-06-03 2020-08-07 浙江金科胶粘制品有限公司 Glue and preparation process thereof
CN112898951A (en) * 2021-02-02 2021-06-04 山西大同大学 Coal dust suppressant with indication function, preparation method and coal dust suppression method

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Publication number Publication date
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Owner name: SHANXI UNIVERISTY LVLIANG POWER SUPPLY COMPANY, ST

Effective date: 20131217

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Effective date: 20131217

C41 Transfer of patent application or patent right or utility model
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Free format text: CORRECT: ADDRESS; FROM: 030006 TAIYUAN, SHAANXI PROVINCE TO: 100031 XICHENG, BEIJING

TR01 Transfer of patent right

Effective date of registration: 20131217

Address after: 100031 Xicheng District West Chang'an Avenue, No. 86, Beijing

Patentee after: State Grid Corporation of China

Patentee after: Shanxi Univeristy

Patentee after: LVLIANG POWER SUPPLY COMPANY, STATE GRID SHANXI ELECTRIC POWER COMPANY

Address before: 030006 Taiyuan, Xiaodian District, Shanxi City Road, No. 92

Patentee before: Shanxi Univeristy