CN105111384B - Engineering resin preparation method based on antislip colour deceleration road surface - Google Patents

Engineering resin preparation method based on antislip colour deceleration road surface Download PDF

Info

Publication number
CN105111384B
CN105111384B CN201510677732.9A CN201510677732A CN105111384B CN 105111384 B CN105111384 B CN 105111384B CN 201510677732 A CN201510677732 A CN 201510677732A CN 105111384 B CN105111384 B CN 105111384B
Authority
CN
China
Prior art keywords
reaction kettle
stirred
engineering resin
platform
preparation
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.)
Active
Application number
CN201510677732.9A
Other languages
Chinese (zh)
Other versions
CN105111384A (en
Inventor
赵壹
赵红林
袁嘉镁
赵梁
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.)
Wuhan Huazhong Science and Technology University New Materials Co., Ltd.
Original Assignee
赵壹
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 赵壹 filed Critical 赵壹
Priority to CN201510677732.9A priority Critical patent/CN105111384B/en
Publication of CN105111384A publication Critical patent/CN105111384A/en
Application granted granted Critical
Publication of CN105111384B publication Critical patent/CN105111384B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The present invention is a kind of engineering resin preparation method based on antislip colour deceleration road surface, includes to prepare vinylite I, prepare auxiliary addition agent II and preparation engineering resin, and totally 3 steps are completed.Vinylite I is prepared, is completed by the reaction kettle A of reaction platform, to obtain pale yellow viscous liquid;Auxiliary addition agent II is prepared, is completed by the reaction kettle B of reaction platform, to obtain colourless transparent solution body;Preparation engineering resin is completed by the reaction kettle C of reaction platform, to obtain the engineering resin of high knot degree.Has the characteristics that easy to use, normal temperature cure, strong adhesive force, high-low temperature resistant, anticorrosive good, environmentally protective.

Description

Engineering resin preparation method based on antislip colour deceleration road surface
Technical field
The present invention relates to a kind of process for preparing resins, especially a kind of engineering resin system based on antislip colour deceleration road surface Preparation Method.
Background technology
Along with the continuous growth of China's vehicle guaranteeding organic quantity and the magnitude of traffic flow, the problem of traffic safety and traffic jam, gets over More to become the insoluble problem of Modern Traffic.It is colored in the solution of the numerous traffic administrations of the developed countries such as America and Europe Anti-skid surface is one of wherein effective solution, and it is extensive to dodge the functions such as reduction of fractions to a common denominator stream, traffic slow-down and traffic prompt Applied to highway, urban road and community's road.Meanwhile for the single dull color of road improvement, being used as city Beautification of landscape means are increasingly taken seriously.
Color anti-skid road surface forms surface layer by obtaining antiskid aggregate in the high polishing value of road crust laying, low wearing valve Construction depth, thus there is higher anti-skid factor (road surface pendulum value up to 75 or more) in supercrust, road surface can be dramatically increased dry It is up to 50% or more, traffic accident can be substantially reduced with the non-skid property of rainy day, shortening braking distance under the conditions of dry With reduction accident harm.
Currently, the engineering adhesive for being widely used in antislip colour deceleration road surface already mainly have epoxies, polyurethanes, Three kinds of acrylic compounds, they respectively have quality, can adapt to different purposes.
Wherein:Epoxies adhesive is mainly made of epoxy resin and curing agent two large divisions, full to improve certain performances The auxiliary materials such as toughener, diluent, accelerating agent, coupling agent can also be added in foot difference purposes.Due to gluing for epoxy adhesive It is high, versatile to connect intensity, less expensive, technique for sticking are easy, once there is the title of " all-purpose adhesive ".After major defect is solidification General partially crisp, antistripping, cracking resistance, shock resistance are poor.
Polyurethane binder is to contain isocyanates (- NCO) and carbamate groups (- NH-COO-) in strand, is had Very strong adhesive strength, while there is wear-resisting, ageing-resistant performance, major defect is legibility water under high temperature, high humidity situation, to drop Low adhesion intensity reduces service life.
Acrylate adhesive is because there are two the common features of its molecular structure:Highly polar and fully saturated property, to Making it have very high pyro-oxidation resistance, 180 DEG C of maximum operation (service) temperature, discontinuously and the short time is using 200 DEG C reachable, 150 DEG C of hot air aging several years performances are without significant change;Since acrylate also has excellent ozone resistants, air-tightness, resistance to Flexion and resistance to breach growth property and uvioresistant discolouration etc., therefore such adhesive has excellent weatherability.It glues simultaneously Intensity height is connect, good film-forming property being capable of room temperature curing.Major defect is poor processability, not water-fast, vapor, soda acid, salting liquid And organic polar solvent.
In conclusion common adhesive cannot all meet the needs that anti-skid surface uses, therefore develop suitable anti-ways The high-performance adhesive in face is of great practical significance.
Invention content
The purpose of the present invention, which is that, overcomes the shortcomings of above-mentioned prior art, to obtain needed for high-performance engineering adhesive Resin, provides that a kind of caking ability is strong, the engineering resin preparation method based on antislip colour deceleration road surface of good weatherability.
A kind of engineering resin preparation method based on antislip colour deceleration road surface, includes S1, S2 and S3, totally 3 steps It completes, wherein:
The step S1 is to prepare vinylite I, and the reaction kettle A of reacted platform is completed;The vinylite I Component is to calculate by weight:
The step S2 is to prepare auxiliary addition agent II, and the reaction kettle B for reacting platform is completed;The auxiliary addition agent II, by weight Amount calculates:
The step S3 is preparation engineering resin, and the reaction kettle C of reacted platform is completed;The component of the engineering resin To calculate by weight:
I 40~80 parts of vinylite
II 30~60 parts of auxiliary addition agent
III 15~30 parts of styrene.
The distinguishing feature of the present invention is easy to use, normal temperature cure, strong adhesive force, high-low temperature resistant, anticorrosive good, green ring It protects.In use, need only uniformly be coated on required engineering resin on road surface, the color ceramic porcelain body of 2~5mm grain sizes is then shed Material, 10~15 minutes just gels, is just fully cured after forty minutes, for people to use to form antislip colour deceleration road surface.
Description of the drawings
Fig. 1 is Whole Work Flow figure of the present invention,
Fig. 2 is that reaction kettle A of the present invention prepares I flow chart of vinyl,
Fig. 3 is that reaction kettle B of the present invention prepares II flow chart of auxiliary addition agent,
Fig. 4 is reaction kettle C preparation engineerings resin flow path figure of the present invention.
Specific implementation mode
~Fig. 4 is please referred to Fig.1, is the specific embodiment of the invention, the specific embodiment of the invention there are 2, is described below:
In order to achieve the above object, the technical solution adopted by the present invention is:
A kind of engineering adhesive preparation method based on antislip colour deceleration road surface includes S1, S2 and S3, and totally 3 walk It is rapid to complete, wherein:
The step S1 is to prepare vinylite I, is completed by the reaction kettle A of reaction platform, to obtain thick pale yellow Liquid;
The step S2 is to prepare auxiliary addition agent II, is completed by the reaction kettle B of reaction platform, to obtain colourless transparent solution Body;
The step S3 is preparation engineering resin, is completed by the reaction kettle C of reaction platform, to obtain highly viscous engineering tree Fat.
The step S1, further includes S11, S12, S13 and S14, totally 4 steps:
The step S11 is stock, to determine the share for preparing dispensing needed for vinylite I, wherein:
The step S12 is that room temperature timing accelerates to be stirred to react, and first from the stock share of step S11, chooses epoxy The corresponding proportioning shares of resin a1 and polyether diols b1, merging are reacted in the reaction kettle A of platform, in 25 DEG C of work temperature of setting Degree and 500~1000r/min accelerate under stirring condition, continue stirring 60 minutes;
The step S13 is that high temperature timing accelerates to be stirred to react, and on the basis of step S12, operating temperature is risen to 90 DEG C~100 DEG C, and maintain 500~1000r/min that stirring condition, continuation is accelerated to be stirred in reaction kettle A 60 minutes;
The step S14 is that heat preservation timing accelerates to be stirred to react, on the basis of step S13, from step S11 dispensing shares In, acrylic acid C1, isobutyl ester d1 and the corresponding proportioning shares of auxiliary agent e1 are chosen, merging is reacted in the reaction kettle A of platform, maintained Under the stirring condition of step S13, continue stirring 180 minutes, to obtain vinylite I.
The step S2, further includes S21, S22 and S23, totally 3 steps:
The step S21 is stock, to determine the share for preparing dispensing needed for auxiliary addition agent II, wherein:
The step S22 is that high temperature timing accelerates to be stirred to react, and chooses methacrylic acid from the stock of step S21 first The corresponding proportioning shares of methyl esters a2 and butyl methacrylate b2, merging are reacted in the reaction kettle B of platform, in 40~50 DEG C of setting Operating temperature and 500~800r/min accelerate under stirring condition, continue in reaction kettle B, are stirred 60 minutes.
The step S23 is that heat preservation timing accelerates to be stirred to react, and on the basis of step S22, is selected from the stock of step S21 Take hydroxypropyl acrylate c2, trimethyol propane triacrylate d2 and the corresponding proportioning shares of styrene e2, merging reaction flat In the reaction kettle B of platform, under the stirring condition of step S22, insulated and stirred work in 30 minutes 1 hour is maintained, is helped with obtaining Agent II.
The step S3, further includes S31, S32 and S33, totally 3 steps:
The step S31 is stock, to determine preparation engineering resin, the quota of required dispensing, wherein:
I 40~80 parts of vinylite
II 30~60 parts of auxiliary addition agent
III 15~30 parts of styrene
The step S32 is that heat preservation timing accelerates base material to be stirred to react, and first turns on the reaction kettle C in reaction platform, and It is 40~60 DEG C that reaction kettle C operating temperatures, which are arranged, then extracts vinyl from reaction kettle A and reaction kettle B successively by step S31 Quota needed for resin I and auxiliary addition agent II is placed in reaction kettle C, under 600~900r/min acceleration environments, is stirred It mixes 30 minutes, to obtain the base material needed for preparation engineering resin.
The step S33 is that heat preservation timing accelerates finely to be stirred to react, and the share needed for styrene III is chosen by step S31 Number, merging are completed in the reaction kettle C of step S32, are maintained the operating temperature and mixing speed of step S32 settings, are stirred 40 ~60 minutes, to obtain required preparation engineering resin.
Embodiment 1
(1) it by 60 parts of epoxy resin, 20 parts of polyether diols under conditions of being stirred continuously, is added in reaction kettle A;
(2) under conditions of being stirred continuously, reaction temperature is increased to 90 DEG C;
(3) auxiliary agent of the acrylic acid of 50 parts by weight, 20 parts of isobutyl ester and 2 parts by weight is added to reaction in 30 minutes 3 hours are kept the temperature in kettle A, reaction product is obtained after the completion of reaction;
(4) butyl methacrylate of the methyl methacrylate of 50 parts by weight and 40 parts by weight is added to reaction kettle B In, and 40~50 DEG C are heated to, under 500~800r/min rate stirring conditions, continuously add 20 parts by weight of acrylic acid hydroxypropyls Ester, 10 parts by weight trimethyol propane triacrylates and 20 parts by weight of styrene stir 30~60min, until the component is complete Full mixing, obtains product;
(5) by 60 parts by weight auxiliary addition agents II obtained by 80 parts by weight of ethylene base resins I obtained by (3) and (4) 600~ It under 900r/min rate stirring conditions, is separately added into reaction kettle C, under conditions of being kept stirring rate, 30 is added in 30 minutes Parts by weight of styrene keeps 600~900r/min rates to stir 40~60 minutes and is uniformly mixed to the component, stops stirring, Obtain the high performance engineering resins.
Embodiment 2
(1) it by 30 parts of epoxy resin, 10 parts of polyether diols under conditions of being stirred continuously, is added in reaction kettle A;
(2) under conditions of being stirred continuously, reaction temperature is increased to 90 DEG C;
(3) auxiliary agent of the acrylic acid of 20 parts by weight, the isobutyl ester of 10 parts by weight and 1 parts by weight is added in 30 minutes 3 hours are kept the temperature in reaction kettle, obtains after the completion of reaction but answers product;
(4) butyl methacrylate of the methyl methacrylate of 30 parts by weight and 20 parts by weight is added to reaction kettle B In, and 40~50 DEG C are heated to, at 500~800r/min, rate stirring condition, continuously add 10 parts by weight of acrylic acid hydroxypropyls Ester, 5 parts by weight trimethyol propane triacrylates and 10 parts by weight of styrene stir 30~60min, until the component is complete It is mixed to get product;
(5) by 30 parts by weight auxiliary addition agents II obtained by 40 parts by weight of ethylene base resins I obtained by (3) and (4) 600~ It under 900r/min rate stirring conditions, is added separately in reaction kettle C, under conditions of being kept stirring rate, adds in 30 minutes 15 parts by weight of styrene keep 600~900r/min rates to stir 40~60 minutes and are uniformly mixed to the component, stop stirring It mixes, obtains the high performance engineering resins.
Above example is to illustrate presently preferred embodiments of the present invention, to illustrate the present invention technical characteristic and can be real Shi Xing, be not limited to the present invention applies for a patent right;Above description simultaneously, for the profession of known the art Personage should can be illustrated and be implemented.Therefore other are under the premise of without departing from disclosed, the equivalent change of completion Or modification, it is all contained within the claim.

Claims (4)

1. a kind of engineering resin preparation method based on antislip colour deceleration road surface includes S1, S2 and S3, totally 3 steps are complete At, wherein:
The step S1 is to prepare vinylite I, and the reaction kettle A of reacted platform is completed;The component of the vinylite I To calculate by weight:
The step S2 is to prepare auxiliary addition agent II, and the reaction kettle B for reacting platform is completed;The auxiliary addition agent II, by weight It calculates:
The step S3 is preparation engineering resin, and the reaction kettle C of reacted platform is completed;The component of the engineering resin is to press Weight calculates:
I 40~80 parts of vinylite
II 30~60 parts of auxiliary addition agent
III 15~30 parts of styrene.
2. the engineering resin preparation method as described in claim 1 based on antislip colour deceleration road surface, it is characterized in that:
The step S1, further includes S11, S12, S13 and S14, totally 4 steps:
The step S11 is stock, to determine the share for preparing dispensing needed for vinylite I;
The step S12 is that room temperature timing accelerates to be stirred to react, and first from the stock share of step S11, chooses epoxy resin The corresponding proportioning shares of a1 and polyether diols b1, merging reaction platform reaction kettle A in, setting 25 DEG C operating temperature and 500~1000r/min accelerates under stirring condition, continues stirring 60 minutes;
The step S13 be high temperature timing accelerate be stirred to react, on the basis of step S12, by operating temperature rise to 90 DEG C~ 100 DEG C, and maintain 500~1000r/min that stirring condition, continuation is accelerated to be stirred in reaction kettle A 60 minutes;
The step S14 is that heat preservation timing accelerates to be stirred to react, on the basis of step S13, from step S11 dispensing shares, Acrylic acid C1, isobutyl ester d1 and the corresponding proportioning shares of auxiliary agent e1 are chosen, merging is reacted in the reaction kettle A of platform, is maintaining to walk Under the stirring condition of rapid S13, continue stirring 180 minutes, to obtain vinylite I.
3. the engineering resin preparation method as described in claim 1 based on antislip colour deceleration road surface, it is characterized in that:
The step S2, further includes S21, S22 and S23, totally 3 steps:
The step S21 is stock, to determine the share for preparing dispensing needed for auxiliary addition agent II;
The step S22 is that high temperature timing accelerates to be stirred to react, and chooses methyl methacrylate from the stock of step S21 first The corresponding proportioning shares of a2 and butyl methacrylate b2, merging are reacted in the reaction kettle B of platform, in 40~50 DEG C of work of setting Temperature and 500~800r/min accelerate under stirring condition, continue in reaction kettle B, are stirred 60 minutes;
The step S23 is that heat preservation timing accelerates to be stirred to react, and on the basis of step S22, third is chosen from the stock of step S21 Olefin(e) acid hydroxypropyl acrylate c2, trimethyol propane triacrylate d2 and the corresponding proportioning shares of styrene e2, merging reaction platform In reaction kettle B, under the stirring condition of step S22, insulated and stirred work in 30 minutes 1 hour is maintained, to obtain auxiliary addition agent II.
4. the engineering resin preparation method as described in claim 1 based on antislip colour deceleration road surface, it is characterized in that:
The step S3, further includes S31, S32 and S33, totally 3 steps:
The step S31 is stock, to determine preparation engineering resin, the quota of required dispensing;
The step S32 is that heat preservation timing accelerates base material to be stirred to react, and first turns on the reaction kettle C in reaction platform, and be arranged Reaction kettle C operating temperatures are 40~60 DEG C, then extract vinylite from reaction kettle A and reaction kettle B successively by step S31 I and auxiliary addition agent II needed for quota, in merging reaction kettle C, under 600~900r/min acceleration environments, be stirred 30 Minute, to obtain the base material needed for preparation engineering resin;
The step S33 is that heat preservation timing accelerates finely to be stirred to react, and the quota needed for styrene III is chosen by step S31, Merging is completed in the reaction kettle C of step S32, is maintained the operating temperature and mixing speed of step S32 settings, is stirred 40~60 Minute, to obtain required preparation engineering resin.
CN201510677732.9A 2015-10-19 2015-10-19 Engineering resin preparation method based on antislip colour deceleration road surface Active CN105111384B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510677732.9A CN105111384B (en) 2015-10-19 2015-10-19 Engineering resin preparation method based on antislip colour deceleration road surface

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510677732.9A CN105111384B (en) 2015-10-19 2015-10-19 Engineering resin preparation method based on antislip colour deceleration road surface

Publications (2)

Publication Number Publication Date
CN105111384A CN105111384A (en) 2015-12-02
CN105111384B true CN105111384B (en) 2018-08-21

Family

ID=54659521

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510677732.9A Active CN105111384B (en) 2015-10-19 2015-10-19 Engineering resin preparation method based on antislip colour deceleration road surface

Country Status (1)

Country Link
CN (1) CN105111384B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106634090B (en) * 2016-09-30 2019-01-25 重庆建科新辉环境技术有限公司 Antislip colour thin layer pavement material and its preparation process based on methacrylic resin MMA

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101747594A (en) * 2009-12-11 2010-06-23 上海新天和树脂有限公司 Epoxy acrylate prepolymer resin and preparation method thereof and application in photocurable coating
CN101928508A (en) * 2010-08-24 2010-12-29 华南理工大学 Polyethylene glycol-modified epoxy acrylate coating and preparation method thereof
CN103173171A (en) * 2011-12-22 2013-06-26 北京新桥技术发展有限公司 Preparation method of colored skid-free road surface layer binding material

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101747594A (en) * 2009-12-11 2010-06-23 上海新天和树脂有限公司 Epoxy acrylate prepolymer resin and preparation method thereof and application in photocurable coating
CN101928508A (en) * 2010-08-24 2010-12-29 华南理工大学 Polyethylene glycol-modified epoxy acrylate coating and preparation method thereof
CN103173171A (en) * 2011-12-22 2013-06-26 北京新桥技术发展有限公司 Preparation method of colored skid-free road surface layer binding material

Also Published As

Publication number Publication date
CN105111384A (en) 2015-12-02

Similar Documents

Publication Publication Date Title
CN109486460A (en) A kind of two-component sealant joint trimming agent and preparation method thereof
CN102796243B (en) Polyurethane modified epoxy resin adhesive, and preparation method and application thereof
CN101225271B (en) Water-based all-purpose adhesive and method for preparing same
CN103666233A (en) Ventilated polyurethane plastic race-track surface layer cementing material
CN108102024A (en) A kind of reactive resin and the pavement marking paint of the solvent-free airless spraying of bi-component
CN104910694A (en) Single-component water-curable polyurethane surface spraying color paste as well as preparation method and application method thereof
KR100933923B1 (en) Paint composition of lane painting and painting process using thereof
CN104449173B (en) Thermoplastic-elastomer-modified polymethyl methacrylate color antiskid paint
CN105111384B (en) Engineering resin preparation method based on antislip colour deceleration road surface
CN101864229A (en) Method for preparing hot-melt quick-drying colorful pavement antiskid paint
CN103388298A (en) Water-based plastic track and preparation method thereof
CN113321449B (en) Manufacturing process of silicon PU for plastic track
CA3065647C (en) Method for producing a printed concrete element
CN106479422A (en) A kind of dual-component aqueous polyurethane binding agent and the construction method in laying stadium
US20080300351A1 (en) Coloring binder for pavement of a road and method for producing the same
CN108192494A (en) One kind is ventilative from knot line type sporting ground material and preparation method
CN109722078A (en) A kind of environment-protecting color roadway applications material and road markings laying method
CN105111895B (en) A kind of preparation method of nano modified abrasion resistant high rigidity floor paint
CN110358481A (en) A kind of chinampa is mated formation special glue and preparation method
CN104877497A (en) Low-optical-transparency powder paint and preparation method thereof
CN109385918B (en) White glue for printing and dyeing and preparation method thereof
KR101905825B1 (en) Mono-fluid type composition for painting traffic lane having excellent visibility
CN117229698B (en) Anti-slip nano adhesive coating applied to pavement
CN113773716B (en) Environment-friendly high-elasticity acrylic plastic track and production method thereof
JPH0626002A (en) Elastic paving body and forming method therefor

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20190830

Address after: 430000 No. 5, No. 3 Road, Huashiyuan Science Park, Donghu New Technology Development Zone, Wuhan City, Hubei Province

Patentee after: Wuhan Huazhong Science and Technology University New Materials Co., Ltd.

Address before: 430074 No. 23-602, Yujia Shandong District, Hongshan District, Wuhan City, Hubei Province

Patentee before: Zhao Yi