KR20170074494A

KR20170074494A - Suspension polymerization compolymer and coating composition using thereof

Info

Publication number: KR20170074494A
Application number: KR1020150183839A
Authority: KR
Inventors: 정요한; 서효정; 전은진
Original assignee: 엘지엠엠에이 주식회사
Priority date: 2015-12-22
Filing date: 2015-12-22
Publication date: 2017-06-30
Also published as: KR101781810B1

Abstract

The present invention relates to a suspension polymerized copolymer of butyl methacrylate and methyl methacrylate, wherein the copolymer has a reduced residual monomer content, and a coating composition containing the same.
The copolymer of the present invention has a low residual monomer content, has an excellent effect in terms of malodor and thermal stability, and is not costly in terms of production because it does not require any additional process or equipment.

Description

TECHNICAL FIELD [0001] The present invention relates to a suspension polymerized copolymer and a coating composition containing the same,

The present invention relates to a suspension polymerized copolymer of butyl methacrylate and methyl methacrylate, wherein the copolymer has a reduced residual monomer content, and a coating composition containing the same.

In the polymer resin prepared using an organic compound as a monomer, the residual monomer does not participate in the reaction but necessarily exists. Exposure to volatile residual monomers for long periods of time will not only jeopardize the safety of workers, but also cause deterioration and deterioration of the final product. Therefore, various research and development are underway to develop a technique for reducing residual monomer in many manufacturers.

U.S. Patent No. 5,973,107 discloses that stepwise introduction of maleic anhydride and peroxide initiators in order to reduce the residual monomer of acrylate is carried out but the polymerization process is complicated and the polymerization of maleic anhydride Drew has a problem in that when it is added to the suspension polymerization using water, it is dissolved in the water to lower the polymerization efficiency.

Japanese Patent No. 2760499 discloses a process for producing a polymer electrolyte membrane by suspension polymerization of a styrene derivative and methacrylate and then removing 5 to 50% of water vapor in the reactant to reduce residual monomer. However, when the amount of energy input to the reactor is large, There is a problem that this increases greatly.

Therefore, there is a need to develop a technique for reducing the residual monomer without increasing the production cost through the monomer composition without adding additional processes and facilities.

United States Patent No. 5973107 Japanese Patent No. 2760499

The present invention aims at lowering the residual monomer content in the production of a suspension polymerization copolymer of butyl methacrylate and methyl methacrylate.

The present invention also provides a coating composition comprising a copolymer of butyl methacrylate and methyl methacrylate having a low residual monomer content and having excellent coating film gloss.

In order to achieve the above object, the present invention relates to a copolymer obtained by suspension polymerization of a resin composition comprising 30 to 70% by weight of butyl methacrylate, 25 to 69% by weight of methyl methacrylate and 1 to 15% by weight of alkyl acrylate will be.

In one embodiment of the present invention, the alkyl acrylate may be a linear or branched (C1-C8) alkyl acrylate.

In one embodiment of the present invention, the resin composition comprises an alkyl methacrylate monomer, a dispersant for suspension polymerization comprising an alkyl (meth) acrylate derivative having a hydrophilic group selected from monomers of the following general formula (1) As shown in Fig.

[Chemical Formula 1]

(Wherein R ³ is H or CH ₃ , M ³ is selected from lithium, sodium, potassium, and ammonium salts, and n is an integer of 1 to 3.)

(2)

(Wherein R ₂ is H or CH ₃ , and m is an integer of 0 to 3)

In one embodiment of the present invention, the dispersant for suspension polymerization is uniformly dispersed in an aqueous solution to have a solid content of 1 to 10% by weight, and may be used in an amount of 0.001 to 1 part by weight based on 100 parts by weight of the total monomer component have.

In one embodiment of the present invention, the copolymer may have a weight average molecular weight of 10,000 to 1,000,000 g / mol.

In one embodiment of the present invention, the copolymer may have a residual monomer content of 3000 ppm or less and a temperature at which a 2% weight loss measured using a thermal gravimetric analysis is 270 to 300 ° C .

The present invention also relates to a coating composition comprising said copolymer.

The copolymer of the present invention has a low residual monomer content, has an excellent effect in terms of malodor and thermal stability, and is not costly in terms of production because it does not require any additional process or equipment.

Hereinafter, the present invention will be described in more detail. In the following description of the present invention, a detailed description of known configurations and functions will be omitted.

Unless otherwise defined, all technical and scientific terms have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention.

Also, the singular forms as used in the specification and the appended claims are intended to include the plural forms as well, unless the context clearly indicates otherwise.

As used herein, the term "copolymer" means that an element referred to herein as a monomer is polymerized and contained as a repeating unit in the copolymer resin. In this specification, the copolymer may be a block copolymer or a random copolymer , But is not limited thereto. The copolymer is not limited to a ternary copolymer comprising an acrylate-based copolymer comprising a copolymer formed by polymerizing the butyl methacrylate monomer, methyl methacrylate monomer and alkyl acrylate monomer as described above , Other monomers other than the above-mentioned monomers may be added as comonomers within the scope of the present invention.

One embodiment of the present invention relates to a suspension-polymerized copolymer of a resin composition comprising 30 to 70% by weight of butyl methacrylate, 25 to 69% by weight of methyl methacrylate and 1 to 15% by weight of alkyl acrylate.

The methyl methacrylate resin is one of the most excellent resins in terms of gloss, transparency, weather resistance and scratch resistance, and satisfies the basic physical properties required for the coating composition. However, since the glass transition temperature is high, the methyl methacrylate resin is fragile at room temperature, It is difficult to apply it to a coating composition because of the disadvantage that cracks are easily generated even when a small impact is applied. Therefore, the present inventors tried to perform suspension polymerization using butyl methacrylate, which is similar to the basic structure of the monomers and has a long substituent group and is easy to control the glass transition temperature even with a small amount of the monomer. However, when the polymerization is carried out using only methyl methacrylate and butyl methacrylate, the reactivity ratios between the monomers are similar, but the reaction heat generated during the polymerization reaction is small and the polymerization is inhibited due to the steric hindrance effect caused by the structure, And there are many residual monomers because they have a structure in which depropagation can occur.

Since butyl methacrylate has a boiling point higher than that of a commonly used coating composition, the volatilization rate varies depending on the drying condition after coating the coating film, and may remain in the coating film depending on the drying conditions.

Accordingly, it has been found that the use of alkyl acrylate can prevent the occurrence of depropagation, thereby reducing the residual monomer content of the suspension polymer and improving the thermal stability, thus completing the present invention.

In one embodiment of the present invention, the butyl methacrylate is preferably used in an amount of 30 to 70 wt%, and the methyl methacrylate is preferably used in an amount of 25 to 69 wt%, more preferably 28 to 68 wt% Do. In the above range, a copolymer having a glass transition temperature of 45 ° C or higher and a 2% weight reduction temperature of 270 ° C or higher can be prepared, and a copolymer for a coating composition having excellent gloss after coating film formation can be produced.

In one embodiment of the present invention, the alkyl acrylate monomer is used for lowering the content of the residual monomer and further increasing the thermal decomposition resistance, and is not particularly limited. Preferably, the alkyl acrylate monomer has a high reactivity ratio to methyl methacrylate And may be, for example, an alkyl acrylate monomer having a linear or branched (C1 to C8) alkyl group, but is not limited thereto. Non-limiting examples of the alkyl methacrylate monomer include methyl acrylate, ethyl acrylate, butyl acrylate, t-butyl acrylate and the like, more preferably methyl acrylate, but are not limited thereto , Or an alkyl acrylate-based monomer which can be used for suspension polymerization.

The amount of the alkyl acrylate is preferably 1 to 15% by weight, more preferably 1 to 8% by weight. When the amount of the monomer is less than 1 wt%, the amount of residual monomer and the thermal decomposition stability are not improved. If the amount is more than 15 wt%, the residual monomer may be increased due to the reactivity ratio of the alkyl acrylate itself.

Another aspect of the invention is the copolymer prepared during, alkyl methacrylate and OH ^- the dispersion stability further includes alkyl meth suspension polymerization dispersing agent for the copolymer in the form of acrylate derivative having a hydrophilic group, such as ^-, SO ₃ The content of the residual monomer can be further lowered.

That is, 0.001 to 1 part by weight of a dispersing agent for suspension polymerization is added to 100 parts by weight of a monomer mixture liquid containing 30 to 70% by weight of butyl methacrylate, 25 to 69% by weight of methyl methacrylate and 1 to 15% by weight of alkyl acrylate The present invention relates to a copolymer obtained by suspension polymerization of a resin composition comprising

In another embodiment of the present invention, the dispersant for suspension polymerization comprises an alkyl methacrylate monomer, an alkyl (meth) acrylate derivative having a hydrophilic group selected from monomers of the following formula (1) and monomers of the following formula .

[Chemical Formula 1]

Wherein R ³ is H or CH ₃ , M ³ is selected from lithium, sodium, potassium and ammonium salts, and n is an integer of 0 to 3.

(2)

(Wherein R ₂ is H or CH ₃ , and m is an integer of 0 to 3)

The dispersant for suspension polymerization is preferably used in an amount of 0.001 to 1 part by weight, more preferably 0.1 to 0.5 parts by weight, based on 100 parts by weight of the total amount of the monomer component. Thereby making it easier to further reduce the content of the residual monomer.

In addition, the solid content of the suspension polymerization dispersant may be uniformly dispersed in the aqueous solution to be 1 to 10 wt%, and more preferably 4 to 6 wt%. Copolymer particles having good properties in the above range can be obtained, excellent polymerization stability, and excellent workability and economical efficiency due to less loss of copolymer particles in washing and drying processes.

In preparing the suspension polymer of the present invention, an inorganic dispersion auxiliary such as calcium carbonate, magnesium carbonate, calcium sulfate, and sodium sulfate may be used as the resin composition, but the present invention is not limited thereto.

Further, it may further contain additives as required. These additives may be used, for example, as long as they can give molecular weight and glass transition temperature of the desired copolymer, such as an initiator, a chain transfer agent, a heat stabilizer, a UV stabilizer and a dispersant.

The initiator can be widely used as long as it is a conventional initiator that can be used in the suspension polymerization of monomers having vinyl groups. For example, azobisisobutyronitrile, 1,1,3,3-tetramethylbutylperoxy-2-ethylhexanoate, 2,2'-azobis (4-methoxy-2,4 -Dimethyl pentanitrile), dimethyl-2,2'-azodiisobutyric acid salt, tert-butylperoxy-3,5,5-trimethylhexanoate, 2,2'-azobis (2- Amidinopropane) dihydrochloride, di-n-propylperoxydicarbobonite, and the like can be used. The content of the initiator is preferably 0.01 to 1 part by weight based on 100 parts by weight of the monomer mixture, but is not limited thereto.

The chain transfer agent can be used for controlling the molecular weight of the copolymer. Non-limiting examples of the chain transfer agent used in the present invention are alkylmercaptans having 1 to 12 carbon atoms in the alkyl group and one thiol functional group or polythiomercapto groups having two or more thiol functional groups. The alkylmercaptan may be, but is not limited to, isopropylmercaptan, tertiary butylmercaptan, normal butylmercaptan, normal amylmercaptan, normal octylmercaptan, and normal dodecylmercaptan. The content of the chain transfer agent may be 0.1 to 5 parts by weight, preferably 0.2 to 1 part by weight, based on 100 parts by weight of the monomer mixture, but is not limited thereto.

The copolymer according to the present invention may have a weight average molecular weight of 10,000 to 1,000,000 g / mol, a glass transition temperature of 30 to 100 ° C, a residual monomer content of 3,000 ppm or less, a thermal gravimetric analysis, The temperature at which the 2% weight loss is measured may be 270 to 300 ° C. And is suitable for use as a coating composition in this range.

Hereinafter, the present invention will be described in more detail based on examples and comparative examples. However, the following examples and comparative examples are merely examples for explaining the present invention in more detail, and the present invention is not limited by the following examples and comparative examples.

In the present invention, the physical property evaluation method is as follows.

One. Determination of residual monomer content

The methyl methacrylate / butyl methacrylate copolymer prepared in Examples and Comparative Examples was dissolved in acetone, the polymer was precipitated in n-hexane, and the remaining solution was filtered and analyzed by GC (Gas chromatography) to determine the residual monomer content Were measured.

2. Measuring thermal degradability

The methyl methacrylate / butyl methacrylate copolymer prepared in Examples and Comparative Examples was heated to 25 ° C to 500 ° C per minute at 10 ° C per minute using a thermal gravimetric analysis, Respectively.

3. Check for smell

The mixture was heated at 105 ° C using a heating loss-measuring device and heated until the volatilization rate reached 0.02% / min to confirm the presence of odor.

X: No odor

O: With smell

4. Glossy after coating formation

Methyl methacrylate / butyl methacrylate copolymer was mixed with a carbon black pigment and an organic solvent methyl ethyl ketone, a primary coat was formed on a transfer paper using a bar coater, dried at 120 ° C, Respectively.

○: Good gloss

Δ: Partial color difference occurred

X: poor gloss

5. Glass transition temperature (Tg)

Was measured using a differential scanning calorimeter (Mettler Toledo) at a rate of 10 ° C / min.

The dispersant for suspension polymerization used in the following examples was prepared by uniformly dispersing a monomer mixture composed of 70 wt% of a monomer represented by the following formula (1) and 30 wt% of a methyl methacrylate monomer in an aqueous solution such that the solid content was 5 wt% .

[Chemical Formula 1]

(Wherein R3 is CH3, M3 is a sodium salt, and n is 1.)

[Example 1]

5 g of a dispersing agent for suspension polymerization (solid content: 5% by weight), disodium hydrogenphosphate (5% by weight), and an aqueous solution of sodium methoxide , 3.75 g of noxohexylmercaptan, and 1.5 g of 2,2'-azobisisobutyronitrile were fed into a water phase while stirring at 500 rpm, and suspension polymerization was carried out secondarily. The first suspension polymerization was carried out at a reaction temperature of 80 ° C, and the polymerization solution was heated to 80 ° C. After 120 minutes, a polymerization peak was generated, and the temperature was elevated to 110 ° C. for 30 minutes to effect secondary suspension polymerization. To prepare a methyl methacrylate / butyl methacrylate copolymer having an average particle size of 200 mu m. The copolymer obtained by suspending was repeatedly washed and dehydrated three times with distilled water and dried in a fluidized bed dryer. The thus obtained methyl methacrylate / butyl methacrylate copolymer was confirmed to have residual monomers, heat decomposition resistance and odor, and gloss failure after drying the coating film, and is shown in Table 1.

[Example 2]

The procedure of Example 1 was repeated except that methyl methacrylate was used at 1 wt% of 28 wt% methyl acrylate. The results are shown in Table 1.

[Example 3]

The procedure of Example 1 was repeated except that ethyl acrylate was used in an amount of 2 wt% instead of methyl acrylate. The results are shown in Table 1.

[Example 4]

The procedure of Example 1 was repeated except that 2 wt% of butyl acrylate was used instead of methyl acrylate. The results are shown in Table 1.

[Example 5]

Butylmethacrylate was used in the same manner as in Example 1 except that 30 wt% methyl methacrylate was used as 68 wt%. The results are shown in Table 1.

[Example 6]

Butyl methacrylate was used in the same manner as in Example 1 except that 30 wt% methyl methacrylate was used at 62 wt% and methyl acrylate was used at 8 wt%. The results are shown in Table 1.

[Example 7]

The results are shown in Table 1, except that the suspension polymerization dispersant was used as polyvinyl alcohol (KH-17, poval).

[Comparative Example 1]

The procedure of Example 1 was repeated except that methyl methacrylate was not used. The results are shown in Table 1.

[Comparative Example 2]

Butyl methacrylate was applied in an amount of 30 wt% methyl methacrylate at 70 wt% and methyl acrylate was not applied. The results are shown in Table 1.

[Comparative Example 3]

The procedure of Example 1 was repeated except that methyl methacrylate was applied at 29.5 wt% and ethyl acrylate was applied at 0.5 wt%. The results are shown in Table 1.

[Comparative Example 4]

Methyl methacrylate as 12 wt.% And ethyl acrylate as 18 wt.%. The results are shown in Table 1.

division Example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 7 Comparative Example 1 Comparative Example 2 Comparative Example 3 Comparative Example 4 Copolymer composition (wt%) Butyl methacrylate 70 70 70 70 30 30 70 70 30 70 70 Methyl methacrylate 28 29 28 28 68 62 28 30 70 29.5 12 Methyl acrylate 2 One - - 2 8 2 - - 0.5 18 Ethyl acrylate - - 2 - - - - - - - - Butyl acrylate - - - 2 - - - - - - - Properties Residual monomer
(ppm) 1600 2100 2500 2600 2500 1800 4500 9800 9600 9000 11500 Presence or absence of smell X X X X X X X ○ ○ ○ ○ 2% weight reduction temperature (캜) 297 273 299 295 298 299 298 198 196 268 295 After film formation
Bad gloss ○ ○ ○ △ ○ ○ △ X X X X Glass transition temperature (캜) 48 49 46 44 89 78 48 49 90 48 23

As shown in Table 1, the methyl methacrylate / butyl methacrylate copolymers of Examples 1 to 6 were found to have improved physical properties such as residual monomers, thermal decomposition resistance, odor and improvement of gloss defect after coating film formation Respectively.

Further, as shown in Examples 1 to 6 and Example 7, in Examples 1 to 6 using a dispersant for suspension polymerization, the residual monomer content was lower and the improved physical properties such as gloss failure improvement after coating film formation .

From the results shown in Table 1, it was found that when the alkyl acrylate was not contained in the butyl methacrylic copolymer (Comparative Examples 1 and 2), the residual monomers were significantly higher than those of the Examples, and the thermal degradation resistance, smell, And the like. This is a result that it is confirmed that the addition of alkyl acrylate in butyl acrylate copolymer polymerization is effective not only in reducing residual monomer but also in improving thermal decomposition resistance.

In addition, the results of Comparative Examples 3 and 4 show that when the alkyl acrylate is added, the heat decomposition resistance is improved. However, when the content is in the range of 1 wt% to 15 wt%, the residual monomer is remarkably higher than those of Examples, And it was confirmed that after the formation, defective gloss and the like were observed.

Claims

A copolymer comprising 30 to 70% by weight of butyl methacrylate, 25 to 69% by weight of methyl methacrylate and 1 to 15% by weight of alkyl acrylate.

The method according to claim 1,
Wherein the alkyl acrylate is a straight chain or branched (C1-C8) alkyl acrylate.

The method according to claim 1,
Wherein said resin composition further comprises an alkyl methacrylate monomer and a dispersing agent for suspension polymerization comprising an alkyl (meth) acrylate derivative having a hydrophilic group selected from the group consisting of a monomer represented by the following formula (1) and a monomer represented by the following formula coalescence.
[Chemical Formula 1]

Wherein R ³ is H or CH ₃ , M ³ is selected from lithium, sodium, potassium and ammonium salts, and n is an integer of 0 to 3.
(2)

(Wherein R ₂ is H or CH ₃ , and m is an integer of 0 to 3)

The method of claim 3,
Wherein the dispersant for suspension polymerization is uniformly dispersed in an aqueous solution such that the solid content is 1 to 10% by weight, and 0.001 to 1 part by weight based on 100 parts by weight of the total monomer component is used.

The method according to claim 1,
Wherein the copolymer has a weight average molecular weight of 10,000 to 1,000,000 g / mol.

The method according to claim 1,
Wherein the copolymer has a residual monomer content of 3,000 ppm or less and a temperature at which a 2% weight loss measured using a thermal gravimetric analysis is 270 to 300 ° C.

A coating composition comprising a copolymer of any one of claims 1 to 6.