KR101821033B1 - Polyurea composition for steel structure coating - Google Patents

Polyurea composition for steel structure coating Download PDF

Info

Publication number
KR101821033B1
KR101821033B1 KR1020160002472A KR20160002472A KR101821033B1 KR 101821033 B1 KR101821033 B1 KR 101821033B1 KR 1020160002472 A KR1020160002472 A KR 1020160002472A KR 20160002472 A KR20160002472 A KR 20160002472A KR 101821033 B1 KR101821033 B1 KR 101821033B1
Authority
KR
South Korea
Prior art keywords
weight
parts
component
polyurea composition
coating
Prior art date
Application number
KR1020160002472A
Other languages
Korean (ko)
Other versions
KR20170083250A (en
Inventor
황주연
엄경일
서기원
Original Assignee
주식회사 케이씨씨
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 주식회사 케이씨씨 filed Critical 주식회사 케이씨씨
Priority to KR1020160002472A priority Critical patent/KR101821033B1/en
Publication of KR20170083250A publication Critical patent/KR20170083250A/en
Application granted granted Critical
Publication of KR101821033B1 publication Critical patent/KR101821033B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/02Polyureas
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers

Abstract

The present invention relates to a polyurea composition for coating a steel structure, and more particularly, to a polyurea composition for coating a steel structure, which is environmentally friendly, has a remarkably low incidence of blistering at the time of coating, Lt; RTI ID = 0.0 > polyurea < / RTI >

Description

Technical Field [0001] The present invention relates to a polyurea composition for coating a steel structure,

The present invention relates to a polyurea composition for coating a steel structure, and more particularly, to a polyurea composition for coating a steel structure, which is environmentally friendly, has a remarkably low incidence of blistering at the time of coating, Lt; RTI ID = 0.0 > polyurea < / RTI >

Korean Patent Application No. 10-2011-0074427 discloses a polyurea resin coating composition for coating inner and outer surfaces of steel pipes and a method for producing the same. In this case, improvement in storage stability and viscosity of the coating composition, Use alkylene carbonate to improve coating leveling during mixing and spraying of paints. However, when the alkylene carbonate is applied to the paint for the inner and outer coating of the steel pipe, there is a problem that blisters tend to occur on the coated surface.

Korean Patent Application No. 10-2006-0127017 discloses a polyurea coating agent for coating a water pipe and a method of manufacturing the same. In order to prevent the viscosity of the prepolymer from being increased or the reaction to proceed easily, The alkylene carbonate is used as a stabilizer (viscosity-reducing agent). However, as described above, there is also a problem that swelling occurs on the coated surface due to the use of alkylene carbonate. Further, in the prepolymer synthesis of urethane or urea, the increase in viscosity due to the explosive raising reaction does not occur when the NCO% is 12% or more.

Further, when the alkylene carbonate is used as in the above-mentioned prior arts, the VOC emission amount according to the small-chamber method is not released and is not environmentally friendly.

It is an object of the present invention to provide a polyurea resin composition which is environmentally friendly because it does not use an alkylene carbonate, has a remarkably low incidence of blistering at the time of coating, has excellent adhesion to steel substrates and is excellent in durability and is particularly suitable for coating steel structures, To provide a composition.

The polyurea composition of the present invention comprises (1) a main part comprising (i) an isocyanate component comprising a modified methylenebisphenyl group and (ii) a polyoxyalkylene glycol component; And (2) a curing agent part comprising (i) a polyamine resin component, (ii) a chain extender component, and (iii) an additive component, wherein the modified methylene bisphenyl group Wherein the content of the isocyanate component is 35 to 77 parts by weight, and the subject portion does not contain an alkylene carbonate.

The polyurea composition according to the present invention is environmentally friendly because it does not use an alkylene carbonate, has a remarkably low incidence of swelling at the time of coating, has excellent adhesion to steel pavement, has excellent durability, and is suitable for sanitary safety standards It meets the hygiene safety standards in accordance with the regulations on certification and conforms to the certification standards of the products subject to environmental labeling in accordance with the Environmental Technology and Environmental Industry Support Act. The standard of KWWA D 113 (waterborne polyurea painted steel pipe and drainage pipe) of the Korean water and sewage societies is based on the standards of 80% confidence level, 90% of products after 20 years use. Satisfies.

Hereinafter, the present invention will be described in detail.

The subject portion of the polyurea composition of the present invention comprises an isocyanate component comprising a modified methylenebisphenyl group wherein the content of isocyanate comprising a modified methylenebisphenyl group is from 35 to 77 parts by weight based on 100 parts by weight of the subject portion , More specifically from 60 to 75 parts by weight, and even more specifically from 65 to 70 parts by weight. If the content of the isocyanate containing the modified methylenebisphenyl group is less than 35 parts by weight based on 100 parts by weight of the main portion, there may be a problem that the mechanical strength of the finally obtained coating film becomes weak, and if it exceeds 77 parts by weight, The viscosity of the coating material may be excessively increased and the coating operation may be difficult, and there may be a problem that the elasticity of the coating film obtained finally decreases.

Examples of the isocyanate containing a modified methylene bisphenyl group usable in the present invention include those having an NCO content of 28.6 to 29.6 wt%, a viscosity of 20 to 60 cps and a specific gravity of 1.195 to 1.230, It is not.

According to one embodiment, as the isocyanate containing the modified methylenebisphenyl group, for example, an isocyanate including a structure in which two methylene phenyl groups are connected by a carbodiimide bond, for example, an isocyanate having the following structure can be used.

Figure 112016002049309-pat00001

According to one embodiment, the subject portion of the polyurea composition of the present invention may further comprise an aromatic isocyanate component other than the isocyanate comprising the modified methylenebisphenyl group. Examples of the aromatic isocyanate component which can be further included include 2,4'-diphenylmethane diisocyanate, 4,4'-diphenylmethane diisocyanate, polymethylene polyphenyl isocyanate, methylene bis (p-cyclohexyl isocyanate) and But the present invention is not limited thereto. The content may be, for example, 1 to 15 parts by weight based on 100 parts by weight of the main portion, but is not limited thereto.

The subject portion of the polyurea composition of the present invention comprises a polyoxyalkylene glycol component.

As the polyoxyalkylene glycol component, for example, polyoxyethylene glycol, polyoxypropylene glycol or a combination thereof can be used. The physical properties of the polyoxyalkylene glycol component are, for example, a molecular weight (MW) of 100 to 3000, a hydroxyl value of 54.0 to 58.0 mgKOH / g, an acid value of 0.03 mgKOH / g or less, and a viscosity of 260 to 340 cps, but is not limited thereto.

The content of the polyoxyalkylene glycol component in the subject portion of the polyurea composition of the present invention may be, for example, 22 to 50 parts by weight, more specifically 25 to 40 parts by weight, based on 100 parts by weight of the main portion , And even more specifically from 30 to 35 parts by weight. If the content of the polyoxyalkylene glycol component is too low, the viscosity of the coating may be excessively increased, which may result in difficulty in coating work, and there may be a problem of reducing the elasticity of the finally obtained coating film. On the other hand, There may be a problem getting rid of.

The main part of the polyurea composition of the present invention does not contain an alkylene carbonate which causes swelling on the coating surface.

The curing agent portion of the polyurea composition of the present invention comprises a polyamine resin component.

As the polyamine resin component, a polyoxyalkylene polyamine resin having 2 to 3 amine functional groups can be used (wherein the alkylene is, for example, C 2 -C 3 alkylene), for example, a polyoxypropylene diamine resin, A rely polyoxypropylenetriamine resin, or a combination thereof. The molecular weight (MW) thereof may be, for example, 300 to 5000, but is not limited thereto.

The content of the polyamine resin component in the curing agent part of the polyurea composition of the present invention may be, for example, 10 to 50 parts by weight, more specifically 20 to 50 parts by weight, based on 100 parts by weight of the curing agent part. If the content of the polyamine resin component is too small, the curing reaction between the main portion and the curing agent becomes uneven, and the coating film may be cured to cause problems such as bubbling or swelling on the surface of the coating film. If the amount is too large, the curing reaction between the main portion and the curing agent portion becomes uneven When the coating is cured, there may be a problem of not sticking and sticking.

The curing agent portion of the polyurea composition of the present invention comprises a chain extender component.

As the chain extender component, an aromatic amine compound may be used, and more preferably, a combination of a single aromatic primary amine, a bis aromatic primary amine, and an aromatic secondary amine may be used. Amine chain extender is a chain extender. It serves to extend the chain of urea bond between isocyanate prepolymer and amine as a curing agent, and allows various physical properties to be controlled depending on the kind. Means a primary amine compound having one aromatic ring in the molecule and the term " bis aromatic primary amine " means that two aromatic rings in the molecule are directly bonded or a divalent linking group ( Such as, for example, a methylene group, etc.).

According to one embodiment, the monoaromatic primary amine may have an amine value of 628 to 634 mgKOH / g, for example, a dialkyltoluenediamine wherein the alkyl is, for example, C 1 -C 4 alkyl For example, diethyltoluenediamine) may be used, and the amount thereof may be, for example, 1 to 10 parts by weight, more specifically 1.5 to 8 parts by weight, based on 100 parts by weight of the curing agent.

According to one embodiment, the bis aromatic primary amine may have an amine value of 153 to 161 mgKOH / g, and examples thereof include methylene bischloroaniline (e.g., 4,4'-methylenebis (2-chloroaniline ) May be used, and the amount thereof may be, for example, 21 to 39 parts by weight, more specifically 25 to 35 parts by weight, based on 100 parts by weight of the curing agent.

According to one embodiment, the aromatic secondary amine having an amine value of 7.4 to 7.6 mgKOH / g may be used. For example, benzene amine may be used. The amount of the aromatic amine to be used may be, based on 100 parts by weight of the curing agent, 6 to 39 parts by weight, and more specifically 10 to 35 parts by weight.

According to one preferred embodiment of the present invention, a combination of dialkyltoluenediamine, benzeneamine and 4,4'-methylenebis (2-chloroaniline) is used as the chain extender component.

The content of the chain extender component in the curing agent portion of the polyurea composition of the present invention may be, for example, 28 to 87 parts by weight, more specifically 35 to 75 parts by weight, based on 100 parts by weight of the curing agent portion. If the content of the chain extender component is too small, there may be a problem that tensile strength and tearing performance of the final coating film obtained become weak. If the content is too large, there is a problem that the final coating film is easily broken or broken by external impact.

The curing agent portion of the polyurea composition of the present invention comprises an additive component.

As the additive component, for example, at least one selected from ultraviolet stabilizers, adhesion promoters, colorants, viscosity regulators, antifoaming agents and surface conditioners can be used.

The amount of the additive component contained in the curing agent portion of the polyurea composition of the present invention may be, for example, 3 to 22 parts by weight, more specifically 5 to 15 parts by weight, based on 100 parts by weight of the curing agent portion, It is not. The ultraviolet light stabilizer may be used in an amount of 0.5 to 3 parts by weight, the adhesion promoting agent may be used in an amount of 0.5 to 5 parts by weight, and the coloring agent may be used in an amount of 2 to 7 parts by weight, based on 100 parts by weight of the curing agent, no.

Hereinafter, the present invention will be described in more detail with reference to Examples. However, the scope of the present invention is not limited to the embodiments.

[ Example ]

1. Preparation of Coating Composition

The components of the composition shown in Table 1 below were used to prepare a coating composition.

Figure 112016002049309-pat00002

Figure 112016002049309-pat00003

Resin 1-1: Modified methylenebisphenylisocyanate (a structure in which two methylene phenyl groups are connected by carbodiimide bond, trade name: Cosmonate LL)

Resin 1-2: 4,4'-diphenylmethane diisocyanate

Resin 1-3: 2,4'-diphenylmethane diisocyanate

Resin 1-4: polyoxypropylene glycol (molecular weight (MW): 2000)

Additive 1-1: alkylene carbonate (ethylene carbonate)

Resin 2-1: Polyoxypropylene diamine

Resin 2-2: Glyceryl polyoxypropylenetriamine

Chain extender 1: diethyltoluenediamine < RTI ID = 0.0 >

Chain extension 2: benzene amine

Chain elongation 3: 4,4'-methylene bis (2-chloroaniline)

Additive 2-1: adhesion promoter (gamma-glycidoxypropyltrimethoxysilane)

Additive 2-2: UV stabilizer (N- (4-ethoxycarbonylphenyl) -N'-methyl-N'-phenylformamidine and bis (1,2,2,6,6- Piperidinyl) -s sebacate < / RTI >

Additive 2-3: Concentrate

2. Evaluation of Physical Properties of Coating Composition

Each of the paints prepared above was coated on a steel substrate having a surface roughness of 30 microns or more and subjected to a blast cleaning and surface treatment at a temperature of Sa2.5 or more and the physical properties of each item described in Table 2 were evaluated. Respectively.

Figure 112016002049309-pat00004

Figure 112016002049309-pat00005

Property evaluation method

1) Appearance

Test method: KS M 5000

Evaluation criteria: There should be no shedding, frying, cracking, swelling, pinholes, etc.

2) Water resistance

Test method: KS N ISO 2812-1

Evaluation criteria: After the water resistance evaluation of 2000 hours, 1.5 mm or more and the adhesion strength should be 4.0 N / mm 2 or more when evaluating the flexural resistance.

3) Salt water silent

Test method Standard number: KS D 9502

Evaluation criteria: After 500 hours of salt water spray test, according to the criteria of ASTM D 1654, KS M ISO 21227-1,3, the non-scribed test showed that the tack area of the coating was within 0.5% Should be within 1.0%.

4) tensile strength, Elongation rate , Phosphorus strength

Test method: KS F 4922

5) Hardness

Test method: ASTM D 2240

6) Bond strength

Test method: ASTM D 4541

7) Impact resistance

1 kg of weight was dropped from a height of 30 cm, and the crack and peeling state of the coating film were visually evaluated

8) Flexibility

Use Ericsson tester to measure the depth of press until the coating is free of defects

Claims (6)

(1) a topical part comprising (i) an isocyanate component comprising a modified methylenebisphenyl group and (ii) a polyoxyalkylene glycol component; And
(2) a curing agent part comprising (i) a polyamine resin component, (ii) a chain extender component and (iii) an additive component,
Wherein the content of the isocyanate component including the modified methylenebisphenyl group in the main part is 35 to 77 parts by weight and the main part does not include an alkylene carbonate,
Wherein the chain extender component is a combination of a single aromatic primary amine, a bis aromatic primary amine and an aromatic secondary amine, the content of the single aromatic primary amine in 100 parts by weight of the curing agent is 1 to 10 parts by weight, Wherein the content of the aromatic primary amine is 21 to 39 parts by weight and the content of the aromatic secondary amine is 6 to 39 parts by weight.
The polyurea composition according to claim 1, wherein the isocyanate comprising a modified methylenebisphenyl group is an isocyanate comprising a structure in which two methylene phenyl groups are connected by carbodiimide bonds. The polyurea composition according to claim 1, wherein the polyoxyalkylene glycol component is polyoxyethylene glycol, polyoxypropylene glycol, or a combination thereof. The polyurea composition according to claim 1, wherein the polyamine resin component is a polyoxyalkylene polyamine resin having 2 to 3 amine functional groups. delete The polyurea composition according to claim 1, wherein the chain extender component is a combination of dialkyltoluenediamine, benzeneamine and 4,4'-methylenebis (2-chloroaniline).
KR1020160002472A 2016-01-08 2016-01-08 Polyurea composition for steel structure coating KR101821033B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1020160002472A KR101821033B1 (en) 2016-01-08 2016-01-08 Polyurea composition for steel structure coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020160002472A KR101821033B1 (en) 2016-01-08 2016-01-08 Polyurea composition for steel structure coating

Publications (2)

Publication Number Publication Date
KR20170083250A KR20170083250A (en) 2017-07-18
KR101821033B1 true KR101821033B1 (en) 2018-01-22

Family

ID=59430710

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020160002472A KR101821033B1 (en) 2016-01-08 2016-01-08 Polyurea composition for steel structure coating

Country Status (1)

Country Link
KR (1) KR101821033B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102635744B1 (en) * 2023-05-04 2024-02-13 (주)씨티기술 Quick-curing type polyurea composition having excellent thermo shield and heat insulation function and quick-curing type thermo shield and heat insulation waterproofing method for concrete structure using the same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102047970B1 (en) * 2019-04-24 2019-11-22 세인스틸 주식회사 steel pipe coating composition of polyurea systematic resin use for Improved durability and water resistance, a steel pipe using thereof
KR102416202B1 (en) 2020-02-06 2022-07-04 부경대학교 산학협력단 Apparatus for classification based on convolution neural network with enhanced accuracy

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000007989A (en) 1998-06-24 2000-01-11 I C K Kk Cold curable composition for forming waterproof coating film
KR101035006B1 (en) * 2011-01-04 2011-05-17 주식회사 케이씨씨 Multilayered paint coating for water treatment facility and its coating method, and water treatment facility comprising the same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000007989A (en) 1998-06-24 2000-01-11 I C K Kk Cold curable composition for forming waterproof coating film
KR101035006B1 (en) * 2011-01-04 2011-05-17 주식회사 케이씨씨 Multilayered paint coating for water treatment facility and its coating method, and water treatment facility comprising the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102635744B1 (en) * 2023-05-04 2024-02-13 (주)씨티기술 Quick-curing type polyurea composition having excellent thermo shield and heat insulation function and quick-curing type thermo shield and heat insulation waterproofing method for concrete structure using the same

Also Published As

Publication number Publication date
KR20170083250A (en) 2017-07-18

Similar Documents

Publication Publication Date Title
KR101691698B1 (en) Epoxy resin composition
KR101197201B1 (en) High speed drying polyurea paint composition having excellent anti-corrosiveness, chemical-resistance and toughness, and construction method using thereof
KR100993243B1 (en) Polyurethane-polyurea paint for inner-coating of water supply pipelines, method of manufacturing the same and method of forming a inner-coating layer of water supply pipelines
KR101029660B1 (en) Polyurea paint composition having excellent workability and superior toughness and method using the same
KR101251066B1 (en) Paint composition having excellent fouling resistance and anti-fouling, and method using the same
JP5632607B2 (en) Protective covering material for concrete structure and method for protecting concrete structure
KR101821033B1 (en) Polyurea composition for steel structure coating
US20160040050A1 (en) Repair liquid for conveyor belts
JP6821486B2 (en) Concrete piece peeling prevention structure, this peeling prevention method and alicyclic polyamine used for these
KR100839933B1 (en) Adhering composition and water-proofing method using the same
KR101197197B1 (en) Polyurea paint composition having excellent anti-corrosiveness, chemical-resistance and workability, and construction method using thereof
JP2009119358A (en) Construction method of covering material
RU2017132326A (en) SYSTEM OF FORMATION OF ELASTOMERIC COMPOSITIONS FOR APPLICATION ON METAL
KR100723775B1 (en) Waterprooping method of concrete structure using normal temperature type polyurea
JP6659385B2 (en) Hydraulic polymer cement composition and floor structure using the same
JP5578061B2 (en) Chain extender for polyurea (urethane) system
KR101581935B1 (en) Paint composition for coating pipeline and concrete pipe having superior strength, and construction method using thereof
JP2021017762A (en) Waterproof coating method of concrete structure
JP2010235652A (en) Solvent-free curable resin composition
KR20150144875A (en) Polyurea paint
JPH11130834A (en) Polyurea resin composition and coating method
JP7398208B2 (en) Method to prevent concrete pieces from falling off
KR101406930B1 (en) Eco-friendly paint composition for ships and heavy duty coating, and construction method using thereof
AU2021216149A1 (en) Polyurethane multi-part kit system
JPS6343432B2 (en)

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E701 Decision to grant or registration of patent right
GRNT Written decision to grant