JPH08253725A - Binder resin composition - Google Patents

Abstract

PURPOSE: To obtain a compsn. which can be applied to various substrates such as plastics, metals, paper, and wood and is useful as a cross-linkable coating compsn. and a primer by cross-linking an oxidation-modified chlorinated polyolefin with a specific compd. CONSTITUTION: An oxidation-modified chlorinated polyolefin is obtd. by dispersing or dissolving a polyolefin (e.g. crystalline polypropylene) in a medium (e.g. water or carbon tetrachloride), chlorinating the polyolefin at 50-120 deg.C under normal pressure or higher in the presence of a catalyst or under exposure to ultraviolet rays, and blowing air, oxygen, or ozone into the reaction system. The modified chlorinated polyolefin is compounded with a curative comprising an arom., aliph., or alicyclic polyisocyanate and/or an epoxy compd. and/or a polyhydric alcohol and a cross-linking catalyst such as a basic catalyst (e.g. a tert. amine) or an organometallic catalyst. The resulting compsn. is used for a coating material, a primer, etc.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a binder resin composition mainly composed of an oxidatively modified chlorinated polyolefin cross-linked product, and more specifically, various plastics including polyolefin, various metals, paper, wood, concrete and the like. To provide a crosslinkable binder resin composition for paints, primers, printing inks and adhesives, which can be applied to the above base material.

[0002]

2. Description of the Related Art Chlorinated polyolefins such as chlorinated polypropylene, chlorinated polyethylene and chlorinated rubber can be easily dissolved in an inexpensive solvent. The solution can be applied, sprayed, dipped, etc. The work is easy and quick drying, the coating film obtained from the solution is acid resistant,
Alkali resistance, weather resistance and flame retardancy are excellent, and those having a chlorine content of 5 to 50 wt% have excellent properties such as good adhesion to a polyolefin resin having poor adhesion. It is used in many fields as a very useful modified resin. Examples thereof include paints, primers, printing inks, coating agents for films and sheets, and adhesives.

However, these chlorinated polyolefins generally have the following drawbacks, and cause various difficulties and limitations in their use. That is, these are poor solvent resistance of the coating film, insufficient strength of the film,
Those with a high chlorine content are brittle and must use a large amount of plasticizer, and those with a low chlorine content have a low softening temperature, so the coating film may peel off even under hot water conditions. It has drawbacks such as poor affinity to the surface of polar substances and difficulty in adhering to metals and wood.

In order to improve these drawbacks, Japanese Patent Publication No.
No. 24316 discloses a method of grafting a monomer having a functional group onto a chlorinated polyolefin.
No. 27968 and JP-A-62-95372 disclose a method of grafting a chlorinated polyolefin with a hydroxyl group-containing acrylic monomer and then crosslinking with an isocyanate compound, and Japanese Patent Publication No. 64-2150 discloses a chlorinated polyolefin with basic nitrogen. A method of grafting the contained acrylic monomer and then crosslinking with an epoxy compound has been proposed.
However, these methods have a drawback that the graft polymerization rate of the above-mentioned monomer to the chlorinated polyolefin is extremely low and a homopolymer is produced, so that a sufficient crosslinked coating film of the chlorinated polyolefin cannot be obtained.

Further, in JP-B-63-50381 and JP-B-1-16414, a chlorinated carboxyl group-containing chlorinated polyolefin obtained by grafting an unsaturated acid anhydride onto a polyolefin is crosslinked with an epoxy compound. Although a method has been proposed, this method also has the disadvantage that the rate of the crosslinking reaction is essentially slow.

It is an object of the present invention to provide a binder resin composition mainly composed of an oxidation-modified chlorinated polyolefin crosslinked product which can solve the above problems. That is, the present invention provides various compositions for paints, primers and printing inks or adhesives which can be applied to various plastics including polyolefins and various metals, paper, wood, concrete and other substrates. The purpose is to do.

[0007]

The present inventors have made an oxidation-modified chlorinated polyolefin obtained by oxidation treatment using at least one or two or more selected from air, oxygen and ozone during chlorination reaction of polyolefin. (I) 2 per molecule
Or more isocyanate groups and / or epoxy groups and / or
Or, it was found that a binder resin composition having a cross-linked product of an oxidation-modified chlorinated polyolefin obtained by crosslinking with a compound (II) having a hydroxyl group as a main binder resin solves the above problems, and has accomplished the present invention. .

The oxidation-modified chlorinated polyolefin used in the present invention includes crystalline polypropylene, amorphous polypropylene, polybutene-1, polypentene-1,4-methylpentene-1, low density or high density polyethylene and ethylene-propylene copolymer. Polymers, ethylene-propylene-diene copolymers, natural rubbers, polyolefins such as polyisoprene are dispersed or dissolved in water or a medium such as carbon tetrachloride or chloroform, and are added under radical irradiation catalyst or ultraviolet irradiation. Chlorination is carried out in the temperature range of 50 to 120 ° C under atmospheric pressure or atmospheric pressure, and air, oxygen or ozone is mixed with gaseous chlorine at the same time, from the beginning or in the middle, or at the end of chlorination, or separately or alternately. Obtained by blowing on.

The progress of oxidation of the oxidation-modified polyolefin is
It can be judged that the absorption around 1730 cm ^-1 measured by an infrared spectrophotometer increases. The degree of oxidation can be confirmed by the functional group index measured by the scale of the following formula, and in order to carry out the present invention, the functional group index is preferably 1 or more.

The compounds having two or more isocyanate groups per molecule used as the crosslinking agent of the present invention include aromatic, aliphatic and alicyclic organic diisocyanates, such as tolylene diisocyanate and xylene diisocyanate. 1,5-naphthalene diisocyanate, 1,4-tetramethylene diisocyanate, 1,6
-Hexamethylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, isophorone diisocyanate, 4,4-dicyclohexylmethane diisocyanate, 1,4-cyclohexyl diisocyanate and the like. In addition, these organic diisocyanates,
It may be used after being modified to an isocyanate derivative such as a buret body, an isocyanurate body or a trimethylolpropane adduct body. Furthermore, a compound having two or more isocyanate groups per molecule, such as a urethane resin having a free isocyanate group obtained by reacting a polymer polyol such as a polyether polyol or a polyester polyol with the above organic diisocyanates, Can be used.

As the compound having an epoxy group, a bisphenol A type or bisphenol F type epoxy resin or a polyhydric alcohol glycidyl ether type, for example, ethylene glycol glycidyl ether, propylene glycol glycidyl ether, glycerol polyglycidyl ether, sorbitol polyglycidyl ether is used. In addition, there is a cycloaliphatic epoxy resin obtained by oxidizing olefins with a peracid. In addition, an acrylic epoxy compound obtained by copolymerizing glycidyl (meth) acrylate and other (meth) acrylates, etc., 2 per molecule
Any compound having at least one epoxy group can be used.

Examples of the compound having a hydroxyl group include diols such as ethylene glycol, propylene glycol, 1,4-butanediol, 1,4-pentanediol, 1,6-hexanediol and 2,5-hexanediol, and glycerin. There are polyhydric alcohols such as trimethylolethane, trimethylolpropane, and pentaerythritol. In addition, any compound having two or more hydroxyl groups per molecule, such as high molecular weight polyols such as polyether polyol and polyester polyol, can be used.

In order to accelerate the crosslinking reaction of the present invention, a third
Basic amines such as pyridine, quinoline, triethylamine, 1,8-diazo-bicyclo-undecene-7 and the like, and organometallic catalysts such as zinc octylate and di-n-butyltin dilaurate may be added. .

The composition of the present invention contains a composition containing a cross-linked product of the above-mentioned oxidation-modified chlorinated polyolefin (I) and compound (II) as a main binder resin, and is used as it is as a coating agent or an adhesive agent. But you can
A pigment, a solvent, and other additives may be added and kneaded and dispersed to be used as a paint or ink. Further, the composition shows balanced performance by itself, but if necessary, an alkyd resin, an acrylic resin, a polyether resin, a polyester resin, a urethane resin or the like may be further added and used.

A feature of the present invention is that during the chlorination reaction of the polyolefin, a functional group is introduced into the chlorinated polyolefin by oxidizing it with air, oxygen, ozone or the like, and two functional groups are added per molecule. The above-mentioned isocyanate group, epoxy group, a binder resin composition mainly composed of a crosslinked product of an oxidation-modified chlorinated polyolefin obtained by crosslinking with a compound having a hydroxyl group, etc. It is to improve solvent resistance, toughness, heat resistance, moisture resistance and the like.

Although the functional group introduced into the chlorinated polyolefin is not clear, it is considered that a carbonyl group, a carboxyl group, an acid chloro group, a peroxide group, a peroxide chlor group and the like are formed during the oxidation treatment. Further, since functional groups are considered to be generated during the cleavage reaction of the polyolefin, it is considered that these functional groups are introduced at the terminal of the chlorinated polyolefin molecule.

[0017]

EXAMPLES Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples.

(Prototype Example-1) Melt index is 14
g / 10 min (Measurement method: ASTM D1238-62
4 kg of isotactic polypropylene of T) was uniformly dissolved in 80 liters of carbon tetrachloride under pressure, and 100 to 11
Chlorination was performed by blowing chlorine gas while irradiating ultraviolet rays at a temperature of 0 ° C. When the chlorine content reached about 20 wt%, the chlorine gas was changed to a mixed gas having a volume ratio of chlorine / air of about 10/90, and chlorination was carried out gently while performing an oxidation treatment. While tracking the above-mentioned functional group index with an infrared spectrophotometer in the middle of the oxidation treatment, the functional group index was 9.5 and 18.
7, the chlorine content is 27.3 wt% and 31.8 wt% respectively
Sample was taken out, carbon tetrachloride was distilled off and replaced with toluene to obtain an oxidation-modified chlorinated polypropylene having a nonvolatile content of 40 wt%.

(Prototype Example-2) The melt index is 70.
g / 10 min (measuring method: JIS K6760) 4 kg of polyethylene was chlorinated under the same conditions as in Prototype Example-1,
When the chlorine content reached about 50 wt%, a mixed gas having a chlorine / oxygen volume ratio of about 45/55 was blown to perform oxidation treatment and chlorination. According to the method of Prototype Example-1, the functional group indexes are 31.2 and 40.5 and the chlorine contents are 6 respectively.
Samples of 9.5 wt% and 69.8 wt% were withdrawn, and carbon tetrachloride was separated by steam distillation and dried to obtain a powder of oxidation-modified chlorinated polyethylene.

(Examples-1 and 2 and Comparative Examples-1 and 2) A paint was prepared using the oxidation-modified chlorinated polypropylene obtained in Prototype Example-1 and a polypropylene plate TX-933A (manufactured by Mitsubishi Petrochemical Co., Ltd.) was prepared. ) Was spray painted. After being dried at room temperature for 15 minutes, forcedly dried at 80 ° C. for 30 minutes and allowed to stand in the room for 1 week, the coating film was tested. Table 1 shows the results. The paint formulation is shown in Table 2.

[0021]

[Table 1] Judgment criteria in the table ◎: Good ○: Almost good ×: Bad × ×: Very bad

Test method ○ Adhesion 100 grids that reach the substrate at 1 mm intervals were made on the coated surface, and cellophane adhesive tape was adhered on it to make 180
It was peeled off in the direction of ° and judged by the extent to which the coating film remained.

○ Warm Water Resistance The coated plate was immersed in hot water of 40 ° C. for 120 hours and 240 hours, and the state of the coating film was examined.

Gasoline resistance (rubbing 100 times) The absorbent cotton was soaked with gasoline and the coated surface was rubbed 100 times to examine the state of the coating film. (Dip 2 hours) Scratch that reaches the substrate on the coated surface (×
Mark) was put in, and it was dipped in gasoline for 2 hours and the state of the coating film was examined.

Bending Resistance The state of the coating film was examined by bending 180 ° with a 1 / 2φ inch mandrel.

○ Impact resistance The impact resistance was examined by using a DuPont type impact tester, using a hammer core of 1 / 2φ inch and a load of 500 g, and dropping it from a height of 50 cm on the coated surface to examine the state of the coating film.

[0027]

[Table 2] ・ Titanium dioxide: trade name R-820, rutile type, manufactured by Ishihara Sangyo Co., Ltd. ・ Isocyanate compound: trade name Desmodur N3390, isocyanate curing agent, hexamethylene diisocyanate system, isocyanurate body, manufactured by Bayer

○ Paint preparation method The resin and titanium dioxide obtained in Prototype Example-1 were 1
After kneading for a period of time, a crosslinking agent and an accelerator were added, and the viscosity was adjusted with xylene so that the temperature was 13 to 15 seconds / 20 ° C. in a No. 4 Ford cup. In the case of Comparative Example, the viscosity was adjusted without adding a crosslinking agent and an accelerator.

(Examples 3 and 4 and Comparative Examples 3 and 4) White ink and red ink were prepared with the oxidation-modified chlorinated polyethylene obtained in Prototype Example-2, and coated on Manila coated paper with coating rod # 4. I worked. After drying at room temperature for 1 day, heat resistance was measured. Table 3 shows the results. The ink formula is shown in Table 4.
Shown in

[0030]

[Table 3] Judgment criteria in the table ◎ No abnormality at all △ Ink transfers to high-quality paper ○ Ink slightly transfers to high-quality paper × Ink transfer causes peeling of paper

○ Test method for heat resistance of ink After a high-quality paper was placed on the ink surface and a heat-seal bar set at each temperature was pressure-bonded for ² kg / cm ² -10 seconds, it was allowed to stand for 30 minutes or more to peel it off. It was judged by the condition of the coated surface at that time.

[0032]

[Table 4]

Ink Preparation Method According to the ink formulation of Table 4, the resin obtained in Prototype Example-2 was dissolved in toluene, the pigment was mixed, and the mixture was kneaded in a sand mill for 2 hours. Next, a crosslinking agent and an accelerator were added, and the viscosity was adjusted with toluene so that the temperature was 20 to 25 seconds / 20 ° C. in a No. 3 Zahn cup. In the case of Comparative Example, the viscosity was adjusted without adding a crosslinking agent and an accelerator.

[0034]

From the results shown in Table 1, the coating films of Comparative Examples 1 and 2 are extremely inferior in hot water resistance and gasoline resistance. However, by crosslinking as in Examples 1 and 2, It can be seen that the property of is significantly improved. In addition, the results shown in Table 3 also show that the heat resistance is improved by crosslinking, which shows that the present invention is useful.

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Claims (2)

[Claims] 1. During the chlorination reaction of a polyolefin, any one of air, oxygen and ozone, or two or three thereof.
Oxidation-modified chlorinated polyolefin (I) obtained by oxidation treatment with a mixture of seeds is obtained by crosslinking with a compound (II) having two or more isocyanate groups and / or epoxy groups and / or hydroxyl groups per molecule. A binder resin composition mainly for a crosslinked product of oxidatively modified chlorinated polyolefin, a primer, a printing ink, and a binder resin composition. 2. A binder resin composition for a paint, a primer, a printing ink or a composition for an adhesive according to claim 1, wherein the chlorine content of the oxidation-modified chlorinated polyolefin (I) is 5 to 75 wt%.