Patent Application
20100113658
The present invention relates to an aqueous adhesive composition which is made solvent-free, and an adhesive using it.
A solvent-type adhesive composition and adhesive using a chloroprene latex have been used in various applications, due to the adaptability to a wide range of adherends and the good balance of adhesion characteristics. However, from the viewpoint of the environmental influence, a demand for solvent-free has been increasing year after year, whereby development of an aqueous adhesive composition and adhesive is demanded. Some proposals have been made for the aqueous adhesive composition and adhesive, but such techniques have various problems to be solved, as compared with the solvent-type adhesive composition and adhesive (Non-patent Document 1)
As a means to improve performance of an aqueous adhesive composition and adhesive using a chloroprene latex, a method is known wherein a pH adjusting agent is added to destabilize a latex and thereby to develop the initial strength in a wet state (Non-patent Document 2, Patent Document 1 and Patent Document 2).
Non-patent Document 1: Secchaku no Gijutsu Vol. 23, No. 4 (2004) Total Vol. 73 (p. 24; item 4.5)
Non-patent Document 2: Secchaku no Gijutsu Vol. 21, No. 4 (2002) Total Vol. 65 (p. 35; item 2.5.5.2)
Patent Document 1: JP-A-2001-19922
Patent Document 2: JP-A-2004-43666
The present invention has an object to provide an aqueous adhesive composition which exhibits sufficient initial strength even in a wet state right after application, and which provides a coating film having sufficient flame retardancy after it is dried, and an adhesive using it.
The present inventors have conducted extensive studies on the above problems, and as a result, they have found that the adhesive composition of the present invention and the adhesive using it, are effective for solving such problems. The present invention has been accomplished on the basis of this discovery.
The present invention provides the following.
The adhesive using the adhesive composition of the present invention, exhibits sufficient initial strength even in a wet state right after application, and provides a coating film having sufficient flame retardancy even after it is dried. The adhesive of the present invention is preferably used as an adhesive for a polyurethane foam material, particularly preferably used as a spray-type adhesive.
Now, the present invention will be described in detail.
The chloroprene latex (A) in the adhesive composition of the present invention is an emulsion wherein a chloroprene polymer is emulsified or dispersed in water by an emulsifier or a dispersant.
The chloroprene polymer is a homopolymer obtained by polymerizing 2-chloro-1,3-butadiene (hereinafter referred to as chloroprene), or a copolymer obtained by polymerizing chloroprene and a monomer which is copolymerizable with chloroprene.
The monomer which is copolymerizable with chloroprene may, for example, be 2,3-dichloro-1,3-butadiene, 1-chloro-1,3-butadiene, butadiene, isoprene, styrene, acrylonitrile, acrylic acid or its ester or methacrylic acid or its ester. It is possible to use two or more of them as the case requires.
The structure of the chloroprene polymer is not particularly limited, and by properly selecting and controlling the polymerization temperature, polymerization initiator, chain transfer agent, polymerization terminator, final polymerization ratio, etc., it is possible to adjust the molecular weight, molecular weight distribution, gel content, molecular terminal structure, crystallization rate, etc.
The emulsifier or dispersant used for emulsion polymerization, is preferably anion-type. It is possible to use the anion-type emulsifier or dispersant together with other emulsifiers or dispersants. By using only those other than the anion-type one, sufficient destabilization may not be attained when a pH adjusting agent is added to form an adhesive, and the initial strength may not be sufficiently developed.
The anion-type emulsifier or dispersant may, for example, be carboxylic acid type or sulfate type. For example, an alkali metal salt of a rosin acid, a C8-20 alkyl sulfonate, an alkylaryl sulfate, a condensate of sodium naphthalenesulfonate and formaldehyde, or a sodium alkyldiphenyl ether disulfonate, may be mentioned.
The anion-type emulsifier or dispersant is most preferably a rosin acid, and any one of wood rosin acid, gum rosin acid, tall oil rosin acid and diproportionated rosin acid, may be used.
The emulsion polymerization using the rosin acid is carried out under high alkalinity, so that, in the chloroprene latex, the rosin acid is present in a form of an alkyl metal salt. Therefore, it is possible to use the rosin acid in a form of an alkyl metal resinate.
The amount of the emulsifier or dispersant to be added is preferably from 0.5 to 10 parts by mass, more preferably from 2 to 6 parts by mass, per 100 parts by mass of the total of monomers to be used.
When the rosin acid is used as the emulsifier, it is preferred to use a sulfate type or sulfonate type anion emulsifier or dispersant together, in order to stabilize the chloroprene latex after addition of the pH adjusting agent. In such a case, the amount of the anion emulsifier or dispersant to be added, other than the rosin acid, is preferably from 0.05 to 5 parts by mass, further preferably from 0.1 to 2 parts by mass, per 100 parts by mass of the total of monomers to be used.
The aromatic phosphate ester type plasticizer (B) is one to be added to impart flame retardancy to a coating film obtained by drying the adhesive composition.
Here, the aromatic phosphate ester type plasticizer is a compound formed by a reaction of phosphorus oxychloride with a phenol or a mixture of a phenol with an alcohol. It may, for example, be triphenyl phosphate, tricresyl phosphate, trixylenyl phosphate, cresyl diphenyl phosphate, 2-ethylhexyl diphenyl phosphate, t-butyl phenyl diphenyl phosphate, isopropyl-modified triaryl phosphate product, bis(t-butylphenyl)phenyl phosphate, tris(t-butylphenyl)phosphate, isopropylphenyl diphenyl phosphate, bis(isopropylphenyl)phenyl phosphate or tris(isopropylphenyl)phosphate. It is preferred to use tricresyl phosphate or cresyl diphenyl phosphate, since it is highly effective in improving flame retardancy of the adhesive.
The amount of (B) to be added is preferably in a range of from 0.1 to 20 parts by mass, more preferably from 1 to 15 parts by mass, further preferably from 1 to 10 parts by mass, per 100 parts by mass of the chloroprene polymer or 100 parts by mass of the copolymer of chloroprene and a monomer copolymerizable with chloroprene, from the viewpoint of developing the effect or improving the adhesive properties of an adhesive to be obtained.
The pH adjusting agent (C) is one to be added to adjust the pH of the adhesive composition or adhesive to be in a range of from 7 to 10, for proper destabilization. The adhesive of the present invention develops good initial strength within such a pH range.
Here, the pH adjusting agent is a weak acid or a buffer, and it may, for example, be an amino acid, boric acid, diluted acetic acid, phosphoric acid, citric acid or glutamic acid. It is preferred to use glycine as one type of amino acids, from the viewpoint of cost, adhesion performance or handling efficiency.
The amount of (C) to be added is not particularly limited, but it should be an amount which makes it possible to adjust the pH of the adhesive to be in a range of from 7 to 10. It is more preferred to use an amount which makes it possible to adjust the pH to be in a range of from 8 to 10.
The halogenated alkyl phosphate ester plasticizer (D) is added when it is desired to further improve flame retardancy of the adhesive. In such a case, the amount of (D) to be used is preferably at most 50 mass %, further preferably at most 30 mass %, based on the total of plasticizers to be added, including the aromatic phosphate ester type plasticizer (B). By adjusting it to be in such a range, compatibility with the chloroprene latex will not be deteriorated, whereby it will be possible to prevent separation of the plasticizers or coagulation of the chloroprene latex.
(D) may, for example, be tris(chloroethyl)phosphate, tris(chloropropyl)phosphate, tris(dichloropropyl)phosphate, tris(tribromoneopentyl)phosphate or tetrakis(2-chloroethyl)ethylene diphosphate.
The proportions of the respective components contained in the adhesive composition of the present invention are such that (B) is from 3 to 18 parts by mass, preferably from 3 to 14 parts by mass, and (C) is from 1 to 20 parts by mass, preferably from 1 to 18 parts by mass, per 100 parts by mass of the solid content of (A).
To the adhesive composition of the present invention, it is possible to incorporate a tackifier resin within such a range that the effect of the present invention is not impaired. In such a case, the type of the tackifier resin is not particularly limited, and it may, for example, be a rosin resin, a rosinate resin, a polymerized rosin resin, an α-pinene resin, a β-pinene resin, a terpene phenol resin, a C5 fraction type petroleum resin, a C9 fraction type petroleum resin, a C5/C9 fraction type petroleum resin, a DCPD type petroleum resin, an alkyl phenol resin, a xylene resin, a coumarone resin or a coumarone-indene resin.
In order to obtain a sufficient initial adhesion power, it is preferred to use resins having a softening point of from 50 to 160° C. Among them, an emulsion of a terpene phenol resin or a rosin acid ester resin, is particularly preferred from the viewpoint of initial strength and water resistance.
The amount of the tackifier resin to be added is preferably at most 10 parts by mass (as dried), per 100 parts by mass of the solid content of a polychloroprene latex, from the viewpoint of maintaining the flame retardancy.
To the adhesive composition of the present invention, it is possible to optionally add e.g. a thickener, a metal oxide, a filler, a film-forming auxiliary agent, an ultraviolet absorber, an antioxidant, a plasticizer, a vulcanizing agent, a vulcanization accelerator, or an antifoam agent, to meet the required performance.
The application of the adhesive of the present invention is not particularly limited. The adhesive is suitably used when bonding various materials such as cement, mortar, slate, cloth, wood material, synthesized rubber material, polyurethane type material, polyvinyl chloride type material or polyolefin type material, and it is particularly suitably used to glue a polyurethane foam type material.
Now, the present invention will be described in further detail with reference to Examples and Comparative Examples, but it should be understood that the present invention is by no means restricted thereto.
In the following description, “parts” and “%” are represented by mass standard, unless otherwise specified.
By using a reactor having a internal volume of 3 L, 5 parts of disproportionated rosin acid, 0.6 part of sodium hydroxide, 0.5 part of potassium hydroxide, 0.3 part of a sodium salt of formaldehyde/naphthalenesulfonate condensate and 0.3 part of sodium hydrogensulfite, were dissolved in 100 parts of water, in a nitrogen atmosphere. With stirring, 100 parts of a chloroprene monomer and 0.14 part of n-dodecyl mercaptan were further added. Then, in a nitrogen atmosphere, polymerization was carried out at 10° C. by using potassium persulfate as an initiator, and when the polymerization ratio became 90%, an emulsion of phenothiazine was added to terminate the polymerization. Heating was carried out under reduced pressure, and an unreacted monomer was removed, followed by concentration to adjust the solid content to be 55%, thereby to obtain a chloroprene latex (CR latex).
To 100 parts by mass (as wetted) of the obtained chloroprene latex (CR latex), 5 parts by mass of tricresyl phosphate (LINDOL XP PLUS, manufactured by Akzo NOBEL) was added with stirring. Then, 6 parts by mass of glycine was added, followed by thorough stirring to obtain an adhesive.
The formulation stability is the state as observed after the obtained adhesive was left to stand in a gear oven at 40° C. for 4 weeks. An adhesive which did not separate or coagulate, and which stayed in the same state as before evaluation of stability without change, was regarded as “good.”
The obtained adhesive was applied on the top surface of an urethane foam having a density of 30 kg/m3 (20 mm in thickness×50 mm in length×50 mm in width), in an amount of 70 g/m2 by a spray. After the prescribed open time, such urethane foams were glued to each other, and after they were left to stand for the prescribed time, the tensile (interfacial peeling) strength was measured.
Here, the tensile strength was measured by using a tensile tester (RTC-1225A, manufactured by ORIENTEC Co., LTD.) by a method in accordance with JIS K6849.
The adhesive was put into a glass bottle, and was stored in a gear oven at 40° C., and then a storage stability test was carried out.
The prepared adhesive was applied on the entire forward end of a flame retardant urethane foam (20 mm in thickness×100 mm in length×20 mm in width) having a density of 30 kg/m3, in an amount of about 70 g/m2 by a spray. After drying it at room temperature for 5 days, a test of flame retardancy was carried out.
The portion of the specimen coated by the adhesive, was put into a flame of a gas burner, and it was taken out 5 seconds later. The burned state of the specimen after being taken out was evaluated. A case where the fire was extinguished immediately after being taken out of the flame, was designated by ⊚, a case where the fire was extinguished within 2 seconds after being taken out, was designated by ◯, and a case where the fire was extinguished within 5 seconds is designated by Δ. A case where the specimen kept on burning more than 5 seconds, was designated by ×.
Examples 2 to 5 were carried out in the same manner as in the Example 1, except for changing the plasticizer used in the tests to one shown in Table 1.
Comparative Examples 1 to 5 were carried out in the same manner as in the Example 1, except for changing the plasticizer used in the tests to one shown in Table 2.
From the results in Table 1, it is evident that the adhesive of the present invention is excellent in initial strength, storage stability and flame retardancy.
In Table 1, Lindol XP Plus represents tricresyl phosphate manufactured by Akzo Nobel; CDP represents cresyl diphenyl phosphate manufactured by DAIHACHI CHEMICAL INDUSTRY Co., LTD; Reofos 65 represents isopropyl-modified triaryl phosphate manufactured by Ajinomoto-Fine-Techno Co., Inc; Fyroll CEF represents tris(chloroethyl)phosphate manufactured by Akzo Nobel; and CRP represents tris(dichloropropyl)phosphate manufactured by DAIHACHI CHEMICAL INDUSTRY Co., LTD.
In Table 2, DBS represents dibutyl sebacate manufactured by TAOKA CHEMICAL Co., LTD.; Empara 40 represents paraffin chloride manufactured by Ajinomoto-Fine-Techno Co., Inc.; TMP represents trimethyl phosphoric acid manufactured by DAIHACHI CHEMICAL INDUSTRY Co., LTD.; TMCPP represents tris(chloropropyl) phosphate manufactured by DAIHACHI CHEMICAL INDUSTRY Co., LTD.; and Fyroll CEF represents tris(chloroethyl)phosphate manufactured by Azko Nobel.
An adhesive obtained by using the adhesive composition of the present invention, develops sufficient initial strength even in a wet state, and has excellent flame retardancy, whereby it is possible to suitably use it in various fields such as woodworking/building materials, shoemaking and cars. Especially, it is most suitable for use to glue e.g. urethane foam materials, and it exhibits excellent initial strength and flame retardancy.
The entire disclosures of Japanese Patent Application No. 2005-355588 filed on December 9, 2005 and Japanese Patent Application No. 2006-23045 filed on Aug. 18, 2006 including specifications, claims and summaries are incorporated herein by reference in their entireties.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2005-355588 | Dec 2005 | JP | national |
| 2006-223045 | Aug 2006 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2006/324574 | 12/8/2006 | WO | 00 | 6/9/2008 |
