WO2021065767A1 - Lamp member resin composition, lamp member, and method for producing lamp member resin composition - Google Patents
Lamp member resin composition, lamp member, and method for producing lamp member resin composition Download PDFInfo
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- WO2021065767A1 WO2021065767A1 PCT/JP2020/036535 JP2020036535W WO2021065767A1 WO 2021065767 A1 WO2021065767 A1 WO 2021065767A1 JP 2020036535 W JP2020036535 W JP 2020036535W WO 2021065767 A1 WO2021065767 A1 WO 2021065767A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/06—Polysulfones; Polyethersulfones
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V3/00—Globes; Bowls; Cover glasses
- F21V3/04—Globes; Bowls; Cover glasses characterised by materials, surface treatments or coatings
- F21V3/06—Globes; Bowls; Cover glasses characterised by materials, surface treatments or coatings characterised by the material
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V7/00—Reflectors for light sources
- F21V7/22—Reflectors for light sources characterised by materials, surface treatments or coatings, e.g. dichroic reflectors
- F21V7/24—Reflectors for light sources characterised by materials, surface treatments or coatings, e.g. dichroic reflectors characterised by the material
Definitions
- the present invention relates to a resin composition for a lamp member that is suitably used as a molding material for a lamp member, a lamp member produced by using the resin composition for a lamp member, and a method for producing a resin composition for a lamp member.
- the present application claims priority based on Japanese Patent Application No. 2019-182112 filed in Japan on October 2, 2019, the contents of which are incorporated herein by reference.
- polyetherimide is the mainstream as a material used for lamp members of automobiles and the like.
- the reflective surface is made of a polyetherimide-based resin containing 0 to 10 parts by weight of glass fiber or an inorganic filler as a reflector for various floodlights such as headlamps of automobiles and the like.
- the reflector is disclosed.
- the present invention has been made to solve the above-mentioned problems, and can be suitably used for a lamp member having excellent heat resistance characteristics and reducing the occurrence of fogging of the lamp, and for molding the lamp member.
- An object of the present invention is to provide a resin composition for a lamp member.
- the present inventors together with aromatic polysulfones, oxides, peroxides, compound oxides and carbon oxides of metals belonging to Group 1 or Group 2 in the long periodic table. It has been found that the fogging of the lamp can be reduced by using at least one selected from the group consisting of, and the present invention has been completed. That is, the present invention has the following aspects.
- a resin composition for a lamp member containing. (2) The resin composition for a lamp member according to (1) above, wherein the reduced viscosity of the component (P) is more than 0.36 (dL / g) and 0.50 (dL / g) or less.
- the present invention it is possible to provide a lamp member having excellent heat resistance characteristics and reducing the occurrence of fogging of the lamp, and a resin composition for the lamp member which can be suitably used for molding the lamp member.
- the resin composition for a lamp member of the embodiment contains (P) component: aromatic polysulfone and (M) component: oxides, peroxides, and compound oxidations of metals belonging to Group 1 or Group 2 in the long periodic table. It contains at least one selected from the group consisting of substances and carbon oxides.
- the lamp member of the embodiment can be molded from the resin composition for the lamp member.
- Examples of the lamp including the lamp member of the embodiment include a lamp including a light source that emits light and heat at the time of lighting and a lamp member that surrounds the light source.
- Examples of the type of the light source include a light emitting diode (LED), a halogen lamp, a HID lamp, and the like.
- the lamp including the lamp member of the embodiment for example, it can be mounted on a vehicle such as an automobile, a motorcycle, a bicycle, or a train and can be used.
- Examples of the type of lamp include a headlamp.
- the current headlamps are roughly classified into two types, a projector type and a reflector type, and the resin composition for a lamp member of the embodiment can be applied to either type.
- a lamp 1 including a light source 12 and a lamp member 3 can be exemplified.
- the lamp member 3 include a lens 14 that collects light emitted from a light source, a reflector 10 that reflects light emitted from a light source 12, and a lens holder 20 that fixes the lens 14.
- the lamp member of the embodiment may further include a housing for accommodating a light source, a reflector, a lens, etc., a lens cover that covers the front surface of the lens and transmits light emitted from the light source, and the like.
- the lamp member can be produced by using the resin composition for the lamp member of the embodiment as a molding material.
- the problematic fogging of the lamp is considered to be derived from the volatile components released from the lamp member in a high temperature environment, and it is presumed that a substance causing fogging adheres to the lens and the lens cover.
- Lenses and lens covers are often made of transparent resin materials, glass, and other materials that are prone to fogging in order to enhance light transmission, and glass lenses tend to be particularly prone to fogging.
- the lamp member molded from the resin composition for the lamp member of the embodiment has excellent heat resistance characteristics and is unlikely to cause fogging of the lamp. Therefore, the lamp member is suitable as a member for surrounding a light source that emits light and heat when lit. ..
- the lamp member of the present embodiment is molded from the resin composition for the lamp member.
- the lamp member of the present embodiment may be a molded body of the resin composition for the lamp member.
- Examples of the method for manufacturing the lamp member include a method having a step of molding the resin composition for the lamp member of the embodiment into a shape corresponding to the lamp member.
- melt molding is preferable, extruding molding, T-die molding, blow molding, injection molding and the like can be exemplified, and a molding method according to the shape of the member and the like can be selected to obtain a resin composition for a lamp member. It can be molded into a shape corresponding to the lamp member.
- the shape corresponding to the lamp member refers to the shape of the lamp member, the shape of a part of the portion constituting the lamp member, the shape of the lamp member or a part thereof, or a shape to which an arbitrary structure is added.
- the lamp member of the present embodiment is preferably an injection molded product using the above-mentioned resin composition as a forming material.
- Examples of the method for manufacturing the lamp member include a method having a step of injection molding the resin composition for the lamp member of the embodiment into a shape corresponding to the lamp member.
- the resin composition for the lamp member is used, for example, at a mold temperature of 120 to 180 ° C. and a resin melting temperature of 330 to 400 ° C., using a general injection molding machine. It can be manufactured by injection molding. Since the lamp member of the embodiment uses the resin composition for the lamp member as the forming material, it has excellent heat resistance characteristics and can make the lamp less likely to be fogged.
- component (P) aromatic polysulfone contained in the resin composition for a lamp member
- component (P) aromatic polysulfone contained in the resin composition for a lamp member
- component (P) aromatic polysulfone contained in the resin composition for a lamp member
- component (P) aromatic polysulfone contained in the resin composition for a lamp member
- component (P) aromatic polysulfone contained in the resin composition for a lamp member
- component (P) aromatic polysulfone contained in the resin composition for a lamp member
- component (P) aromatic polysulfone contained in the resin composition for a lamp member
- Examples of the resin include a compound represented by the following general formula (I) and a compound represented by the following general formula (II).
- R 1 independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 20 carbon atoms, or a halogen atom
- n1 is 0 to 4 of an integer
- each R 1 identical or different phenylene groups may be the same or different
- each n1 identical or different phenylene groups may be the same or different from each other.
- R 2 independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 20 carbon atoms, or a halogen atom
- n2 is 0 to 4
- Each R 2 of the same or different phenylene groups may be the same or different from each other, and each n 2 of the same or different phenylene groups may be the same or different from each other.
- the alkyl group having 1 to 10 carbon atoms in R 1 and R 2 may be linear or branched, and may be, for example, a methyl group, an ethyl group, an n-propyl group, an isopropyl group or an n-butyl group. , Isobutyl group, s-butyl group, t-butyl group, n-hexyl group, 2-ethylhexyl group, n-octyl group, n-decyl group and the like.
- the alkyl group in R 1 and R 2 is preferably an alkyl group having 1 to 6 carbon atoms.
- the aryl group having 6 to 20 carbon atoms in R 1 and R 2 include a phenyl group, an o-tolyl group, an m-tolyl group, a p-tolyl group, a 1-naphthyl group, a 2-naphthyl group and the like. Be done.
- halogen atom in R 1 and R 2 examples include a fluorine atom, a chlorine atom, a bromine atom, an iodine atom and the like.
- n1 and n2 are independently integers of 0 to 4, preferably 0 to 2, and more preferably 0 to 1.
- Examples of commercially available products of the compound represented by the general formula (I) include Sumitomo Chemical Co., Ltd.'s trade name Sumika Excel PES 3600P, 4100P and 4800P.
- the terminal structure of the aromatic polysulfone resin is determined according to the production method of each resin, and examples thereof include, but are not limited to, Cl, OH, and OR (R is an alkyl group).
- the ratio of the content of the component (P) to the total mass (100% by mass) of the resin composition for a lamp member may be, for example, 50% by mass or more, and may be 50 to 99.9% by mass. It may be 70 to 99.5% by mass, and may be 80 to 99.0% by mass.
- the reduced viscosity of the component (P) is preferably more than 0.36 (dL / g) and 0.50 (dL / g) or less, and is 0.38 (dL / g) or more and 0.48 (dL / g) or more. ) Or less, and more preferably 0.40 (dL / g) or more and 0.45 (dL / g) or less.
- the reducing viscosity of the component (P) exceeds or exceeds the above lower limit value, the occurrence of fogging of the lamp is further prevented and the heat resistance of the resin composition for the lamp member is also improved.
- the reducing viscosity of the component (P) is not more than the above upper limit value, the handling and moldability of the resin composition for a lamp member can be improved.
- the reduced viscosity of the component (P) can be measured by the following method.
- the viscosity ( ⁇ ) of 1 dL of a solution prepared by dissolving 1 g of the component (P) in N, N-dimethylformamide is measured at 25 ° C. using an Ostwald type viscosity tube.
- the viscosity ( ⁇ 0) of N, N-dimethylformamide, which is a solvent is measured at 25 ° C. using an Ostwald type viscosity tube.
- the specific viscosity ratio (( ⁇ - ⁇ 0) / ⁇ 0) is obtained from the viscosity ( ⁇ ) of the solution and the viscosity ( ⁇ 0) of the solvent.
- the reduced viscosity (dL / g) is determined by dividing this specific viscosity by the concentration of the solution (about 1 g / dL).
- the resin composition for a lamp member of the embodiment is imparted with strength applicable to the lamp member exposed to high heat, and can exhibit excellent heat resistance characteristics.
- the 180 ° C. bending strength of the cured product of the resin composition for lamp members can be adopted.
- the 180 ° C. bending strength is preferably 35 MPa or more, more preferably 40 MPa or more, further preferably 50 MPa or more, and particularly preferably 55 MPa or more.
- the upper limit of the bending strength at 180 ° C. is not particularly limited, but may be 70 MPa or less, 65 MPa or less, and 60 MPa or less.
- the numerical range of the above numerical values may be, for example, 35 MPa or more and 70 MPa or less, 40 MPa or more and 65 MPa or less, 50 MPa or more and 65 MPa or less, and 55 MPa or more and 60 MPa or less.
- the value of the bending strength at 180 ° C. shall be the value obtained by the method and measurement conditions shown below.
- the glass transition temperature (° C.) of the aromatic polysulfone of the embodiment is preferably 200 ° C. or higher, and more preferably 215 ° C. or higher.
- the glass transition temperature (° C.) is an index for determining the degree of heat resistance of aromatic polysulfone, and it can be said that the higher the temperature, the better the heat resistance.
- the glass transition temperature can be calculated by a differential scanning calorimetry device according to JIS-K7121.
- component (M) contained in the resin composition for lamp members selected from the group consisting of oxides, peroxides, compound oxides and carbon oxides of metals belonging to Group 1 or Group 2 in the long periodic table. At least one kind to be described will be described.
- M 2 O or M'O As the oxide of the metal belonging to Group 1 or Group 2 in the long periodic table, the general formula M 2 O or M'O (in these formulas, M is Group 1 and M'is a metal element belonging to Group 2. ) Can be exemplified.
- M'O 2 As the peroxide of the metal belonging to Group 1 or Group 2 in the long periodic table, the general formula M'O 2 (in these formulas, M is Group 1 and M'is a metal element belonging to Group 2. ) Can be exemplified.
- M is preferably at least one selected from the group consisting of Na and K.
- M' is preferably at least one selected from the group consisting of Mg, Ca, and Ba, more preferably at least one selected from the group consisting of Mg, and Ca, and even more preferably Mg.
- the compound oxide containing a metal belonging to Group 1 or Group 2 in the long periodic table is the general formula M 2 O ⁇ mM ′′ O 2 ⁇ xH 2 O, M'O ⁇ mM'' O 2 ⁇ xH 2.
- M is preferably K
- M' is preferably at least one selected from the group consisting of Mg, Ca, and Ba. Examples of this include, but are not limited to, wollastonite, attapulsite, sericite, mica, potassium titanate, barium titanate and the like.
- Carbonates containing metals belonging to Group 1 or Group 2 in the Long Periodic Table are the general formulas M 2 CO 3 , M'CO 3 or M' ⁇ M'' (CO 3 ) 2 (in the formula, M is Group 1 and M'and M'' can be exemplified by those represented by metal elements belonging to Group 2.
- M is preferably K
- M'and M' is preferably at least one selected from the group consisting of Mg, Ca, and Ba. Examples of this include, but are not limited to, potassium carbonate, calcium carbonate, dolomite and the like.
- layered double hydroxide can be exemplified as a carbonate containing a metal belonging to Group 1 or Group 2 in the long periodic table.
- Examples of the layered double hydroxide include hydrotalcite. These can be used alone or in combination of two or more. Of these, hydrotalcite is preferred.
- the formula for hydrotalcite is: Mg 1-y Al y (OH ) 2 (CO 3) y / 2 ⁇ qH 2 O [Representing numerical values of 0 ⁇ y ⁇ 0.5 and 0 ⁇ q in the formula] It is represented by.
- the hydrotalcite may be a natural product or a synthetic product, and can be used regardless of its crystal structure, crystal particle size, and the like.
- the oxides peroxides, double oxides and carbon oxides of metals belonging to Group 1 or Group 2 in the long periodic table
- a mixture or solid solution thereof may be used.
- the mixture or solid solution of the metal oxide include calcined dolomite (mixture containing calcium oxide and magnesium oxide), calcined hydrotalcite (solid solution of calcium oxide and aluminum oxide) and the like.
- Examples on the market include calcined dolomite ("KT” manufactured by Yoshizawa Lime Industry Co., Ltd.), calcium oxide ("Moistop # 10" manufactured by Sankyo Seiko Co., Ltd., etc.), magnesium oxide ("Kyowa Chemical Industry Co., Ltd.” Kyowa Mag MF-150 “,” Kyowa Mag MF-30 “,” Pure Mag FNMG “manufactured by Tateho Chemical Industries, Ltd., etc.), Lightly baked magnesium oxide ("# 500", “# 1000", “# 5000” manufactured by Tateho Chemical Industries, Ltd.
- component (M) those exhibiting alkalinity are preferable from the viewpoint of neutralization with acid gas (sulfite gas), and for example, magnesium oxide, calcium oxide, barium oxide, barium peroxide, wollastonite, attapulsite, and seri. Cyto, mica, potassium titanate, barium titanate, potassium carbonate, calcium carbonate, dolomite, hydrotalcite, calcined hydrotalcite and the like are preferable.
- one type may be contained alone, or two or more types may be contained in combination.
- the component (M) is an oxide of a metal belonging to Group 1 or Group 2 in the long periodic table. It is preferable that the component (M) is magnesium oxide.
- the content of the component (M) is preferably 0.5 to 10 parts by mass, preferably 0.7 to 10 parts by mass, and 1 to 1 to 10 parts by mass with respect to 100 parts by mass of the component (P). It is more preferably 7 parts by mass, further preferably 1 to 5 parts by mass, and particularly preferably 1.5 to 4 parts by mass.
- the upper limit value and the lower limit value of the numerical range of the content of the component (M) exemplified above can be freely combined.
- the resin composition for a lamp member containing the component (M) at the above lower limit value or more can more effectively reduce the occurrence of fogging of the lamp.
- the heat resistance of the composition for the lamp member is good, and the addition of the component (M) causes an increase in the melt viscosity of the resin composition for the lamp member. It is difficult to stabilize the quality of the resin composition for lamp members.
- melt viscosity of the resin composition for a lamp member the melt viscosity at 380 ° C. measured using a capillary rheometer can be adopted, and the melt viscosity can be measured by the measurement method described below.
- melt viscosity of resin composition for lamp members As the melt viscosity of the resin composition for a lamp member at 380 ° C., the melt viscosity at 380 ° C. measured using a capillary rheometer is measured. A capillary having a diameter of 1.0 mm and a length of 10 mm was used, and 20 g of a pellet-shaped resin composition for a lamp member dried at 150 ° C. for 4 hours was placed in a cylinder set at 380 ° C. and conformed to ISO 11443. It is assumed that the melt viscosity at a shear rate of 12000s- 1 has been measured.
- the inventors have found that the suppression of the increase in melt viscosity is more pronounced as the content of chlorine (Cl) contained in the resin composition for lamp members is higher, and the chlorine (Cl) is more pronounced.
- an aromatic polysulfone composition having a content of more than 2000% by mass, preferably 3000% by mass or more and 5000% by mass or less, the content of the component (M) is 0 with respect to 100 parts by mass of the component (P). .5 to 10 parts by mass, preferably 0.7 to 10 parts by mass, more preferably 1 to 7 parts by mass, further preferably 1 to 5 parts by mass, 1 It is particularly preferably .5 to 4 parts by mass.
- the upper limit value and the lower limit value of the numerical range of the content of the component (M) exemplified above can be freely combined.
- the content of chlorine (Cl) contained in the resin composition for lamp members is preferably 2000 mass ppm or less, and preferably 1700 mass ppm or less. Is more preferable, and 1500 mass ppm or less is further preferable.
- the lower limit of the content of chlorine (Cl) contained in the resin composition for lamp members may be, for example, 100 ppm by mass or more, or 500 ppm or more.
- the preferable range of the content of chlorine (Cl) contained in the resin composition for lamp members is, for example, 100 mass ppm or more and 2000 mass ppm or less, and 100 mass ppm or more and 1700 mass ppm or less. It may be 500 ppm or more and 1500 mass ppm or less.
- Chlorine (Cl) contained in the above resin composition for lamp members may correspond to the Cl atom of the aromatic polysulfone at its terminal.
- Aromatic polysulfone is usually produced by polycondensation reaction of an aromatic dihalogenosulfone compound and an aromatic dihydroxy compound in the coexistence of a base and a reaction solvent (see, for example, Japanese Patent Application Laid-Open No. 2012-509375). .. That is, the aromatic polysulfone obtained by the polycondensation reaction of the aromatic dihalogenosulfone compound and the aromatic dihydroxy compound has a halogen atom or a phenolic hydroxyl group at the terminal thereof.
- the content of chlorine (Cl) contained in the resin composition for lamp members can be adjusted by, for example, adopting the method disclosed in Japanese Patent Application Laid-Open No. 2018-070698.
- the polycondensation reaction is carried out in the presence of at least one aromatic end cap agent.
- aromatic terminal cap agent examples include those disclosed in Japanese Patent Application Laid-Open No. 2018-070698.
- it does not contain a structure that is reactive to halogen atoms or easily generates radicals, and is easily available.
- 4-phenylphenol, 1-naphthol, 2-naphthol, and 4-phenoxyphenol are preferable.
- the polycondensation reaction is carried out in the coexistence of at least one aromatic terminal cap agent to obtain aromatic polysulfone, and then the solvent is removed, and the precipitate containing aromatic polysulfone is repeatedly washed with a poor solvent. By doing so, chlorine (Cl) can be efficiently removed.
- the inventors have found that the above-mentioned increase in melt viscosity is unlikely to occur by using magnesium oxide as the component (M), as shown in Examples described later. This is probably because the addition of a metal oxide may cause the polymerization reaction of aromatic polysulfone having a Cl atom at the end to proceed, but the use of magnesium oxide makes it difficult for such a polymerization reaction to proceed. Inferred.
- the component (M) is magnesium oxide from the viewpoint that the occurrence of fogging of the lamp can be reduced particularly effectively and the above-mentioned increase in melt viscosity is unlikely to occur.
- Many of the lamp members are relatively large, and in their molding, appropriate fluidity of the composition is often required. It can be said that the fact that the melt viscosity of the resin composition for a lamp member of the embodiment is unlikely to increase is a suitable feature as a composition used for manufacturing a lamp member. Further, from the viewpoint of suppressing an increase in the melt viscosity, it is preferable that the content of the component (M) is in the range exemplified above.
- the reduced viscosity of the component (P) is more than 0.36 (dL / g) and 0.50 (dL / g) or less, and the component (M) is magnesium oxide. It is preferable that the heat resistance of the resin composition for the lamp member and the reduction of the occurrence of fogging of the lamp are further satisfactorily achieved.
- the reduced viscosity of the component (P) is more than 0.36 (dL / g) and 0.50 (dL / g) or less
- the component (M) is magnesium oxide.
- the content of the component (M) is 1 to 10 parts by mass with respect to 100 parts by mass of the component (P), which improves the heat resistance of the resin composition for lamp members and reduces the occurrence of fogging of the lamp. , Even better achieved, especially preferred.
- the resin composition for a lamp member may contain other components that do not correspond to any of the components (P) and (M) as long as the effects of the present invention are not impaired.
- other components examples include fillers, additives, resins other than the component (P) (hereinafter, may be referred to as “other resins”) and the like. These other components may be contained alone or in combination of two or more.
- the filler may be a fibrous filler or a granular filler. Further, the filler may be an inorganic filler or an organic filler.
- fibrous inorganic filler examples include glass fibers; carbon fibers such as pan-based carbon fibers and pitch-based carbon fibers; ceramic fibers such as silica fibers, alumina fibers and silica-alumina fibers; and metal fibers such as stainless steel fibers. Be done. Further, whiskers such as potassium titanate whiskers, barium titanate whiskers, wollast night whiskers, aluminum borate whiskers, silicon nitride whiskers, and silicon carbide whiskers can also be mentioned.
- glass fibers include those manufactured by various methods such as chopped glass fibers and milled glass fibers.
- carbon fibers examples include pan-based carbon fibers made from polyacrylonitrile, pitch-based carbon fibers made from coal tar and petroleum pitch, cellulose-based carbon fibers made from viscose rayon and cellulose acetate, and hydrocarbons. Examples thereof include vapor-phase growth-based carbon fibers made from rayon and the like.
- the carbon fiber may be chopped carbon fiber or milled carbon fiber.
- Examples of granular inorganic fillers include silica, alumina, titanium oxide, boron nitride, silicon carbide, calcium carbonate and the like.
- additives include metering stabilizers, mold release agents, antioxidants, heat stabilizers, UV absorbers, antistatic agents, surfactants, flame retardants and colorants.
- thermoplastic resins other than liquid crystal polymers such as polypropylene, polyamide, polyester, polyphenylene sulfide, polyetherketone, polycarbonate, polyphenylene ether, polyetherimide, and fluororesin; phenolic resin, epoxy resin, and polyimide resin.
- Thermoplastic resins such as cyanate resin.
- the resin composition for a lamp member of the present embodiment can be produced by mixing the component (P), the component (M) and other components used as necessary in a batch or in an appropriate order.
- the method for producing a resin composition for a lamp member of the present embodiment includes a step of mixing the component (P) and the component (M).
- Examples of the component (P) and the component (M) include those described in the above ⁇ Resin composition for lamp member >>.
- the amount of the component (M) used is preferably 0.5 to 10 parts by mass with respect to 100 parts by mass of the component (P), and more preferably 1 to 7 parts by mass. It is preferable to mix in a ratio of 1.5 to 4 parts by mass, more preferably.
- the resin composition for a lamp member obtained by mixing the component (M) at a ratio of the lower limit value or more can more effectively reduce the occurrence of fogging of the lamp. Further, the resin composition for lamp members obtained by mixing the component (M) at a ratio of not more than the above upper limit has good heat resistance of the composition for lamp members, and the melt viscosity due to the addition of the component (M). Is unlikely to increase, and it is easy to stabilize the quality of the resin composition for lamp members.
- the resin composition for a lamp member of the present embodiment is provided as pelletized by melting and kneading the component (P), the component (M) and other components used as necessary using an extruder. It is possible.
- the resin composition for lamp members of the embodiment is selected from the group consisting of (M) component: oxides, peroxides, compound oxides and carbon oxides of metals belonging to Group 1 or Group 2 in the long periodic table. By containing at least one of these, the effect of reducing the fogging of the lamp is exhibited.
- the effect of reducing fogging of the lamp in the resin composition for the lamp member can be confirmed without actually manufacturing the lamp.
- a test device imitating a lamp can be used, and the resin composition for a lamp member is cured in a container assuming a space volume of a housing for accommodating a light source. After storing the object, the inside of the container is heated, and the comparison result of the amount of components adhering to the inside of the container before and after heating and the comparison result of the actual degree of cloudiness can be obtained. Then, as compared with the resin composition containing the component (P), the resin composition according to the embodiment obtained by further adding the component (M) to the resin composition adhered to the inside of the container after heating. It can be determined that the effect of reducing the fogging of the lamp is achieved when the amount of the component is reduced, the degree of fogging is low, or the heating time until the occurrence of fogging is short.
- the mechanism by which the component (M) exerts the effect of reducing the fogging of the lamp is inferred as follows.
- sulfurous acid (SO 2 ) gas is generated, and it is considered that, for example, sodium sulfate that has reacted with Na contained in the glass lens of the lamp adheres to the glass lens. .. It is considered that by adding the above component (M), the component (M) reacts with sulfur dioxide gas and the generation of sulfur dioxide gas can be suppressed.
- the resin composition for the lamp member of the embodiment contains the component (P)
- the molded product molded from the composition for the lamp of the embodiment exhibits excellent heat resistance characteristics.
- the resin composition for the lamp member of the embodiment contains the component (M)
- the reduced viscosity of the component (P) is more than 0.36 (dL / g)
- the effect of reducing the occurrence of fogging of the lamp is further enhanced, and further, more suitable heat resistance characteristics as a lamp member are exhibited.
- the reduced viscosity of the component (P) is 0.50 (dL / g) or less, the molding characteristics for molding the lamp member become better.
- the component (M) is magnesium oxide
- the effect of reducing the occurrence of fogging of the lamp is further enhanced, and the molding characteristics for molding the lamp member are also improved.
- the composition for a lamp of the embodiment has very excellent properties as a composition used for molding a lamp member.
- the specific viscosity (( ⁇ - ⁇ 0 ) / ⁇ 0 ) was obtained from the viscosity ( ⁇ ) of the solution and the viscosity ( ⁇ 0 ) of the solvent, and this specific viscosity was calculated as the concentration of the solution (about 1 g / dL). ) To determine the reduced viscosity (dL / g) of the resin.
- Pellets of the resin composition for lamp members are made into a flat plate with a width of 64 mm, a length of 64 mm, and a thickness of 1 mm at a cylinder temperature of 360 ° C and a mold temperature of 150 ° C using an injection molding machine (PS40E5ASE, Nissei Resin Industry Co., Ltd.).
- the test piece was molded and cut into 10 mm squares, which was used as the test piece.
- 2 g of the test piece was placed in a petri dish having a diameter of 32 mm and a height of 15 mm, soda-lime glass was placed on the petri dish, heated on a hot plate set at 260 ° C., and the time until fogging occurred on the glass was measured. .. The longer this time is, the less fogging is.
- melt viscosity of the resin composition for a lamp member As the melt viscosity of the resin composition for a lamp member, the melt viscosity at 380 ° C. measured using a capillary rheometer was measured. A capillary of 1.0 mm ⁇ ⁇ 10 mm was used, and 20 g of pellets of a resin composition for a lamp member dried at 150 ° C. for 4 hours was placed in a cylinder set at 380 ° C., and melted at a shear rate of 12000s -1 in accordance with ISO 11443. The viscosity was measured.
- the glass transition temperature was calculated by a method according to JIS-K7121 using a differential scanning calorimetry device (DSC-50 manufactured by Shimadzu Corporation). About 10 mg of the sample was weighed and raised to 400 ° C. at a heating rate of 10 ° C./min, cooled to 50 ° C., and again raised to 400 ° C. at a heating rate of 10 ° C./min. From the DSC chart obtained by the second temperature rise, the glass transition temperature was calculated by a method according to JIS-K7121.
- Example 1 pellets of the resin composition for lamp members were produced in the same manner as in Example 1 except that the type of PES, the type of metal oxide, and the blending amount thereof were changed as shown in Table 1.
- "-" In the table means that the component is not included.
- calcium oxide Inoue Lime Industry Co., Ltd. (VESTA-PP) was used.
- Sumika Excel PES3600P a polyether sulfone (PES) manufactured by Sumitomo Chemical Co., Ltd., a glass transition temperature of 225 ° C., and a reduction viscosity of 0.36 dL / g were used.
- PES polyether sulfone
- the resin compositions for lamp members of Examples 1 to 10 containing the components (P) and (M) are the resin compositions for lamp members of Comparative Examples 1 and 2 not containing the component (M). In comparison, the occurrence of fogging in the fogging test was suppressed.
- Example 2 Comparison between Example 2 and Example 8, comparison between Example 4 and Example 9, comparison between Example 5 and Example 10, comparison between Example 6 and Example 11, and Example 7 and According to the comparison with Example 12, the higher the reduced viscosity of PES of the component (P), the more the occurrence of fogging in the fogging test was suppressed.
- Example 2 and Example 6 the case where MgO is used as the component (M) is the case where CaO is used as the component (M). Rather, the occurrence of fogging in the fogging test was suppressed.
- melt viscosity of the composition was less likely to increase than in Examples 5 to 6 in which CaO was used as the component (M). It turned out that.
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Abstract
Description
本発明は、ランプ部材の成形材料として好適に用いられるランプ部材用樹脂組成物、前記ランプ部材用樹脂組成物を用いて作製したランプ部材、及びランプ部材用樹脂組成物の製造方法に関する。
本願は、2019年10月2日に、日本に出願された特願2019-182112号に基づき優先権を主張し、その内容をここに援用する。
The present invention relates to a resin composition for a lamp member that is suitably used as a molding material for a lamp member, a lamp member produced by using the resin composition for a lamp member, and a method for producing a resin composition for a lamp member.
The present application claims priority based on Japanese Patent Application No. 2019-182112 filed in Japan on October 2, 2019, the contents of which are incorporated herein by reference.
自動車等のランプ部材に用いられる材料として、現状、ポリエーテルイミドが主流となっている。
例えば、特許文献1には、自動車等のヘッドランプをはじめ、各種投光器具のリフレクタとして、反射面が、0~10重量部のガラス繊維もしくは無機フィラーを含むポリエーテルイミド系樹脂から構成されてなるリフレクタが開示されている。
At present, polyetherimide is the mainstream as a material used for lamp members of automobiles and the like.
For example, in
しかし、ポリエーテルイミドでも耐熱性能が十分でなく、ポリエーテルイミドに代わる、ランプ部材に適用可能な優れた耐熱特性を有する材料の開発についての要求がある。
本発明者らの検討の結果、ポリエーテルイミドよりもガラス転移温度が高く、優れた耐熱特性を有する、芳香族ポリスルホンが、ランプ部材用として有用な材料であることを見出した。
However, even polyetherimide does not have sufficient heat resistance, and there is a demand for the development of a material having excellent heat resistance that can be applied to lamp members in place of polyetherimide.
As a result of the studies by the present inventors, it has been found that aromatic polysulfone, which has a higher glass transition temperature than polyetherimide and has excellent heat resistance, is a useful material for lamp members.
しかし、上記芳香族ポリスルホンを、光源から発せられる高熱にさらされるランプ部材に適用しようとすると、ランプに曇りが発生してしまうという問題があった。 However, when the above aromatic polysulfone is applied to a lamp member exposed to high heat emitted from a light source, there is a problem that the lamp becomes cloudy.
本発明は、上記のような問題点を解決するためになされたものであり、優れた耐熱特性を有し、ランプの曇り発生が低減されたランプ部材、及びその成形に好適に用いることのできるランプ部材用樹脂組成物を提供することを目的とする。 The present invention has been made to solve the above-mentioned problems, and can be suitably used for a lamp member having excellent heat resistance characteristics and reducing the occurrence of fogging of the lamp, and for molding the lamp member. An object of the present invention is to provide a resin composition for a lamp member.
本発明者らは、上記課題を解決すべく鋭意検討した結果、芳香族ポリスルホンとともに、長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種を用いることで、ランプの曇りを低減可能であることを見出し、本発明を完成するに至った。
すなわち、本発明は以下の態様を有する。
As a result of diligent studies to solve the above problems, the present inventors, together with aromatic polysulfones, oxides, peroxides, compound oxides and carbon oxides of metals belonging to
That is, the present invention has the following aspects.
(1)(P)成分:芳香族ポリスルホンと、
(M)成分:長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種と、
を含有する、ランプ部材用樹脂組成物。
(2)前記(P)成分の還元粘度が、0.36(dL/g)超、0.50(dL/g)以下である、前記(1)に記載のランプ部材用樹脂組成物。
(3)前記(M)成分が、長周期型周期表における1族又は2族に属する金属の酸化物である、前記(1)又は(2)に記載のランプ部材用樹脂組成物。
(4)前記(M)成分が、酸化マグネシウムである、前記(3)に記載のランプ部材用樹脂組成物。
(5)前記(M)成分の含有量が、前記(P)成分100質量部に対して0.5~10質量部である、前記(1)~(4)のいずれか一つに記載のランプ部材用樹脂組成物。
(6)前記(1)~(5)のいずれか一つに記載のランプ部材用樹脂組成物より成形されたランプ部材。
(7)(P)成分:芳香族ポリスルホンと、
(M)成分:長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種と、
を混合する工程を有する、ランプ部材用樹脂組成物の製造方法。
(1) Ingredients (P): Aromatic polysulfone and
Component (M): At least one selected from the group consisting of oxides, peroxides, double oxides and carbon oxides of metals belonging to
A resin composition for a lamp member containing.
(2) The resin composition for a lamp member according to (1) above, wherein the reduced viscosity of the component (P) is more than 0.36 (dL / g) and 0.50 (dL / g) or less.
(3) The resin composition for a lamp member according to (1) or (2) above, wherein the component (M) is an oxide of a metal belonging to
(4) The resin composition for a lamp member according to (3) above, wherein the component (M) is magnesium oxide.
(5) The above-mentioned (1) to (4), wherein the content of the component (M) is 0.5 to 10 parts by mass with respect to 100 parts by mass of the component (P). Resin composition for lamp members.
(6) A lamp member molded from the resin composition for a lamp member according to any one of (1) to (5) above.
(7) Ingredients (P): Aromatic polysulfone and
Component (M): At least one selected from the group consisting of oxides, peroxides, double oxides and carbon oxides of metals belonging to
A method for producing a resin composition for a lamp member, which comprises a step of mixing.
本発明によれば、優れた耐熱特性を有し、ランプの曇り発生が低減されたランプ部材、及びその成形に好適に用いることのできるランプ部材用樹脂組成物を提供できる。 According to the present invention, it is possible to provide a lamp member having excellent heat resistance characteristics and reducing the occurrence of fogging of the lamp, and a resin composition for the lamp member which can be suitably used for molding the lamp member.
以下、本発明のランプ部材用樹脂組成物、ランプ部材、及びランプ部材用樹脂組成物の製造方法の実施形態を説明する。 Hereinafter, embodiments of the method for producing the resin composition for lamp members, the lamp member, and the resin composition for lamp members of the present invention will be described.
≪ランプ部材用樹脂組成物≫
実施形態のランプ部材用樹脂組成物は、(P)成分:芳香族ポリスルホンと、(M)成分:長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種と、を含有する。
<< Resin composition for lamp members >>
The resin composition for a lamp member of the embodiment contains (P) component: aromatic polysulfone and (M) component: oxides, peroxides, and compound oxidations of metals belonging to
<ランプ部材>
実施形態のランプ部材は、ランプ部材用樹脂組成物から成形することができる。
実施形態のランプ部材を備えるランプとしては、点灯時に光及び熱を発する光源と、その光源を囲うランプ部材と、を備えたものを例示できる。
<Lamp member>
The lamp member of the embodiment can be molded from the resin composition for the lamp member.
Examples of the lamp including the lamp member of the embodiment include a lamp including a light source that emits light and heat at the time of lighting and a lamp member that surrounds the light source.
上記光源の種類としては、例えば、発光ダイオード(LED)、ハロゲンランプ、HIDランプ等が挙げられる。 Examples of the type of the light source include a light emitting diode (LED), a halogen lamp, a HID lamp, and the like.
実施形態のランプ部材を備えるランプとしては、例えば、自動車や、バイク、自転車、電車等の車両に搭載されて、使用可能である。ランプの種類としては、例えばヘッドランプが挙げられる。
現行のヘッドランプは、プロジェクタータイプとリフレクタータイプの2種類に大別され、実施形態のランプ部材用樹脂組成物は、どちらのタイプにも適用可能である。
As the lamp including the lamp member of the embodiment, for example, it can be mounted on a vehicle such as an automobile, a motorcycle, a bicycle, or a train and can be used. Examples of the type of lamp include a headlamp.
The current headlamps are roughly classified into two types, a projector type and a reflector type, and the resin composition for a lamp member of the embodiment can be applied to either type.
例えば、上記構成を備えるプロジェクタータイプのランプとしては、図1に示すように、光源12と、ランプ部材3と、を備えるランプ1を例示できる。ランプ部材3としては、光源から発せられた光を集光させるレンズ14、光源12から発せられた光を反射するリフレクタ10、及びレンズ14を固定するレンズホルダー20を例示できる。
For example, as a projector type lamp having the above configuration, as shown in FIG. 1, a
実施形態のランプ部材は、さらに、光源、リフレクタ、レンズ等を収容するハウジングや、レンズ前面を覆い光源から発せられた光を透過させるレンズカバー等を有していてもよい。 The lamp member of the embodiment may further include a housing for accommodating a light source, a reflector, a lens, etc., a lens cover that covers the front surface of the lens and transmits light emitted from the light source, and the like.
上記ランプ部材は、実施形態のランプ部材用樹脂組成物を成形材料として作製することができる。問題となるランプの曇りとは、高温環境下でランプ部材から放出された揮発性成分に由来するものと考えられ、レンズやレンズカバーに曇りの原因となる物質が付着したものと推定される。レンズやレンズカバーは、光の透過を高めるため、透明樹脂素材やガラスなどの曇りが目立ちやすい材料から構成されることが多く、ガラス製のレンズは、特に曇りやすい傾向にある。
実施形態のランプ部材用樹脂組成物から成形されたランプ部材は、優れた耐熱特性を有し、ランプの曇り発生の要因となり難いため、点灯時に光及び熱を発する光源を囲う部材として好適である。
The lamp member can be produced by using the resin composition for the lamp member of the embodiment as a molding material. The problematic fogging of the lamp is considered to be derived from the volatile components released from the lamp member in a high temperature environment, and it is presumed that a substance causing fogging adheres to the lens and the lens cover. Lenses and lens covers are often made of transparent resin materials, glass, and other materials that are prone to fogging in order to enhance light transmission, and glass lenses tend to be particularly prone to fogging.
The lamp member molded from the resin composition for the lamp member of the embodiment has excellent heat resistance characteristics and is unlikely to cause fogging of the lamp. Therefore, the lamp member is suitable as a member for surrounding a light source that emits light and heat when lit. ..
本実施形態のランプ部材は、上記ランプ部材用樹脂組成物より成形されたものである。 本実施形態のランプ部材は、上記ランプ部材用樹脂組成物の成形体であってよい。 The lamp member of the present embodiment is molded from the resin composition for the lamp member. The lamp member of the present embodiment may be a molded body of the resin composition for the lamp member.
ランプ部材の製造方法として、実施形態のランプ部材用樹脂組成物をランプ部材に対応する形状に成形する工程を有する方法が挙げられる。 Examples of the method for manufacturing the lamp member include a method having a step of molding the resin composition for the lamp member of the embodiment into a shape corresponding to the lamp member.
当該成形方法としては、溶融成形が好ましく、押し出し成形、T-ダイ成形、ブロー成形、射出成形等を例示でき、部材の形状等に応じた成形方法を選択して、ランプ部材用樹脂組成物をランプ部材に対応する形状に成形することができる。
なお、ランプ部材に対応する形状とは、ランプ部材の形状のほか、ランプ部材を構成する部分の一部の形状、ランプ部材又はその一部又に任意の構造が付加された形状を指す。
As the molding method, melt molding is preferable, extruding molding, T-die molding, blow molding, injection molding and the like can be exemplified, and a molding method according to the shape of the member and the like can be selected to obtain a resin composition for a lamp member. It can be molded into a shape corresponding to the lamp member.
The shape corresponding to the lamp member refers to the shape of the lamp member, the shape of a part of the portion constituting the lamp member, the shape of the lamp member or a part thereof, or a shape to which an arbitrary structure is added.
本実施形態のランプ部材は、上述の樹脂組成物を形成材料とする射出成形体であることが好ましい。 The lamp member of the present embodiment is preferably an injection molded product using the above-mentioned resin composition as a forming material.
ランプ部材の製造方法として、実施形態のランプ部材用樹脂組成物をランプ部材に対応する形状に射出成形する工程を有する方法が挙げられる。
射出成形品であるランプ部材は、上記ランプ部材用樹脂組成物を、例えば、金型温度を120~180℃で、樹脂の溶融温度を330~400℃で、一般的な射出成形機を用いて射出成形して製造することができる。実施形態のランプ部材は、ランプ部材用樹脂組成物を形成材料として用いているので、優れた耐熱特性を有し、ランプの曇りを発生し難いものとすることができる。
Examples of the method for manufacturing the lamp member include a method having a step of injection molding the resin composition for the lamp member of the embodiment into a shape corresponding to the lamp member.
For the lamp member, which is an injection-molded product, the resin composition for the lamp member is used, for example, at a mold temperature of 120 to 180 ° C. and a resin melting temperature of 330 to 400 ° C., using a general injection molding machine. It can be manufactured by injection molding. Since the lamp member of the embodiment uses the resin composition for the lamp member as the forming material, it has excellent heat resistance characteristics and can make the lamp less likely to be fogged.
<(P)成分>
以下、ランプ部材用樹脂組成物に含有される(P)成分:芳香族ポリスルホンについて説明する。(P)成分:芳香族ポリスルホンとしては、スルホニル基(-SO2-)とアリーレン基(-Ar-)とエーテル結合(-O-)とがこの順で結合した構造を少なくとも含む構成単位、を有する樹脂が挙げられる。
<(P) component>
Hereinafter, the component (P): aromatic polysulfone contained in the resin composition for a lamp member will be described. Component (P): As the aromatic polysulfone, a structural unit containing at least a structure in which a sulfonyl group (-SO 2- ), an arylene group (-Ar-) and an ether bond (-O-) are bonded in this order. Examples thereof include resins having.
当該樹脂としては、下記一般式(I)で表される化合物、及び下記一般式(II)で表される化合物を例示できる。 Examples of the resin include a compound represented by the following general formula (I) and a compound represented by the following general formula (II).
(式中、R1は、それぞれ独立に、炭素数1~10のアルキル基、炭素数2~10のアルケニル基、炭素数6~20のアリール基、又はハロゲン原子を表し、n1は0~4の整数であり、同一の又は異なるフェニレン基の各R1は互いに同一でも異なっていてもよく、同一の又は異なるフェニレン基の各n1は互いに同一でも異なっていてもよい。) (In the formula, R 1 independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 20 carbon atoms, or a halogen atom, and n1 is 0 to 4 of an integer, each R 1 identical or different phenylene groups may be the same or different, each n1 identical or different phenylene groups may be the same or different from each other.)
(式中、R2は、それぞれ独立に、炭素数1~10のアルキル基、炭素数2~10のアルケニル基、炭素数6~20のアリール基、又はハロゲン原子を表し、n2は0~4の整数であり、同一の又は異なるフェニレン基の各R2は互いに同一でも異なっていてもよく、同一の又は異なるフェニレン基の各n2は互いに同一でも異なっていてもよい。) (In the formula, R 2 independently represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an aryl group having 6 to 20 carbon atoms, or a halogen atom, and n2 is 0 to 4 Each R 2 of the same or different phenylene groups may be the same or different from each other, and each n 2 of the same or different phenylene groups may be the same or different from each other.)
R1及びR2における、前記炭素数1~10のアルキル基としては、直鎖状又は分岐鎖状であってよく、例えばメチル基、エチル基、n-プロピル基、イソプロピル基、n-ブチル基、イソブチル基、s-ブチル基、t-ブチル基、n-ヘキシル基、2-エチルヘキシル基、n-オクチル基、n-デシル基等が挙げられる。
R1及びR2におけるアルキル基は、炭素数1~6のアルキル基が好ましい、
The alkyl group having 1 to 10 carbon atoms in R 1 and R 2 may be linear or branched, and may be, for example, a methyl group, an ethyl group, an n-propyl group, an isopropyl group or an n-butyl group. , Isobutyl group, s-butyl group, t-butyl group, n-hexyl group, 2-ethylhexyl group, n-octyl group, n-decyl group and the like.
The alkyl group in R 1 and R 2 is preferably an alkyl group having 1 to 6 carbon atoms.
R1及びR2における、炭素数2~10のアルケニル基としては、R1及びR2において例示した前記アルキル基において、いずれか一つの炭素原子間の単結合(C-C)が、二重結合(C=C)に置換されたものが例示でき、二重結合の位置は限定されない。
R1及びR2における、前記炭素数6~20のアリール基としては、例えばフェニル基、o-トリル基、m-トリル基、p-トリル基、1-ナフチル基、2-ナフチル基等が挙げられる。
R1及びR2における、前記ハロゲン原子としては、フッ素原子、塩素原子、臭素原子、ヨウ素原子等が挙げられる。
n1及びn2は、それぞれ独立に、0~4の整数であり、0~2が好ましく、0~1がより好ましい。
In R 1 and R 2, the alkenyl group having 2 to 10 carbon atoms, in the alkyl group exemplified in R 1 and R 2, single bond between any one of the carbon atoms (C-C) is a double The one substituted with the bond (C = C) can be exemplified, and the position of the double bond is not limited.
Examples of the aryl group having 6 to 20 carbon atoms in R 1 and R 2 include a phenyl group, an o-tolyl group, an m-tolyl group, a p-tolyl group, a 1-naphthyl group, a 2-naphthyl group and the like. Be done.
Examples of the halogen atom in R 1 and R 2 include a fluorine atom, a chlorine atom, a bromine atom, an iodine atom and the like.
n1 and n2 are independently integers of 0 to 4, preferably 0 to 2, and more preferably 0 to 1.
一般式(I)で表される化合物の市販品の例としては、住友化学株式会社の商品名スミカエクセルPES 3600P、4100Pおよび4800Pが挙げられる。芳香族ポリサルホン樹脂の末端構造は、各々の樹脂の製法に従って決まるものであり、例えば、Cl、OH、OR(Rはアルキル基)などが挙げられるが、これらに限定されるものではない。 Examples of commercially available products of the compound represented by the general formula (I) include Sumitomo Chemical Co., Ltd.'s trade name Sumika Excel PES 3600P, 4100P and 4800P. The terminal structure of the aromatic polysulfone resin is determined according to the production method of each resin, and examples thereof include, but are not limited to, Cl, OH, and OR (R is an alkyl group).
ランプ部材用樹脂組成物の総質量(100質量%)における、前記(P)成分の含有量の割合は、例えば50質量%以上であってよく、50~99.9質量%であってよく、70~99.5質量%であってよく、80~99.0質量%であってよい。 The ratio of the content of the component (P) to the total mass (100% by mass) of the resin composition for a lamp member may be, for example, 50% by mass or more, and may be 50 to 99.9% by mass. It may be 70 to 99.5% by mass, and may be 80 to 99.0% by mass.
前記(P)成分の還元粘度は、0.36(dL/g)超0.50(dL/g)以下であることが好ましく、0.38(dL/g)以上0.48(dL/g)以下であることがより好ましく、0.40(dL/g)以上0.45(dL/g)以下であることがさらに好ましい。
前記(P)成分の還元粘度が上記下限値超又は以上であることにより、ランプの曇り発生がより防止されるとともに、ランプ部材用樹脂組成物の耐熱性も向上する。前記(P)成分の還元粘度が上記上限値以下であることにより、ランプ部材用樹脂組成物の取り扱いや成形性を良好とすることができる。
The reduced viscosity of the component (P) is preferably more than 0.36 (dL / g) and 0.50 (dL / g) or less, and is 0.38 (dL / g) or more and 0.48 (dL / g) or more. ) Or less, and more preferably 0.40 (dL / g) or more and 0.45 (dL / g) or less.
When the reducing viscosity of the component (P) exceeds or exceeds the above lower limit value, the occurrence of fogging of the lamp is further prevented and the heat resistance of the resin composition for the lamp member is also improved. When the reducing viscosity of the component (P) is not more than the above upper limit value, the handling and moldability of the resin composition for a lamp member can be improved.
(P)成分の還元粘度は以下の方法により測定できる。
(P)成分1gをN,N-ジメチルホルムアミドに溶解した溶液1dLの粘度(η)を、オストワルド型粘度管を用いて、25℃で測定する。
また、溶媒であるN,N-ジメチルホルムアミドの粘度(η0)を、オストワルド型粘度管を用いて、25℃で測定する。
前記溶液の粘度(η)と前記溶媒の粘度(η0)とから、比粘性率((η-η0)/η0)を求める。この比粘性率を、前記溶液の濃度(約1g/dL)で除することにより、還元粘度(dL/g)を求める。
The reduced viscosity of the component (P) can be measured by the following method.
The viscosity (η) of 1 dL of a solution prepared by dissolving 1 g of the component (P) in N, N-dimethylformamide is measured at 25 ° C. using an Ostwald type viscosity tube.
Further, the viscosity (η0) of N, N-dimethylformamide, which is a solvent, is measured at 25 ° C. using an Ostwald type viscosity tube.
The specific viscosity ratio ((η-η0) / η0) is obtained from the viscosity (η) of the solution and the viscosity (η0) of the solvent. The reduced viscosity (dL / g) is determined by dividing this specific viscosity by the concentration of the solution (about 1 g / dL).
実施形態のランプ部材用樹脂組成物は、(P)成分を含有することで、高熱にさらされるランプ部材に適用可能な強度が付与され、優れた耐熱特性を発揮できる。 By containing the component (P), the resin composition for a lamp member of the embodiment is imparted with strength applicable to the lamp member exposed to high heat, and can exhibit excellent heat resistance characteristics.
実施形態のランプ部材用樹脂組成物の耐熱特性を示す指標としては、ランプ部材用樹脂組成物の硬化物の180℃曲げ強度を採用することができる。上記180℃曲げ強度は、35MPa以上が好ましく、40MPa以上がより好ましく、50MPa以上がさらに好ましく、55MPa以上が特に好ましい。
180℃曲げ強度の上限値は特に制限されるものではないが、70MPa以下であってよく、65MPa以下であってよく、60MPa以下であってよい。
上記の数値の数値範囲としては、例えば、35MPa以上70MPa以下であってよく、40MPa以上65MPa以下であってよく、50MPa以上65MPa以下であってよく、55MPa以上60MPa以下であってよい。
180℃曲げ強度の値は、以下に示す方法及び測定条件により得られた値とする。
As an index showing the heat resistance characteristics of the resin composition for lamp members of the embodiment, the 180 ° C. bending strength of the cured product of the resin composition for lamp members can be adopted. The 180 ° C. bending strength is preferably 35 MPa or more, more preferably 40 MPa or more, further preferably 50 MPa or more, and particularly preferably 55 MPa or more.
The upper limit of the bending strength at 180 ° C. is not particularly limited, but may be 70 MPa or less, 65 MPa or less, and 60 MPa or less.
The numerical range of the above numerical values may be, for example, 35 MPa or more and 70 MPa or less, 40 MPa or more and 65 MPa or less, 50 MPa or more and 65 MPa or less, and 55 MPa or more and 60 MPa or less.
The value of the bending strength at 180 ° C. shall be the value obtained by the method and measurement conditions shown below.
(180℃曲げ強度の測定)
ランプ部材用樹脂組成物を成形材料として、射出成形機を用い、シリンダー温度360℃、金型温度150℃にて、幅12.7mm、長さ127mm、厚み6.4mmの棒状試験片を成形し、ASTM D790に準拠して、試験速度2mm/分、支点間距離100mm、圧子の先端の半径5mmにて、曲げ試験を実施することで、180℃での曲げ強度を測定する。曲げ強度の値については、3本の試験片についての結果の平均値を採用する。
(Measurement of bending strength at 180 ° C)
Using an injection molding machine using a resin composition for a lamp member as a molding material, a rod-shaped test piece having a width of 12.7 mm, a length of 127 mm, and a thickness of 6.4 mm is molded at a cylinder temperature of 360 ° C. and a mold temperature of 150 ° C. , ASTM D790, the bending strength at 180 ° C. is measured by performing the bending test at a test speed of 2 mm / min, a distance between fulcrums of 100 mm, and a radius of 5 mm at the tip of the indenter. For the value of bending strength, the average value of the results for the three test pieces is adopted.
実施形態の芳香族ポリスルホンのガラス転移温度(℃)は、200℃以上であることが好ましく、215℃以上であることがより好ましい。ガラス転移温度(℃)は、芳香族ポリスルホンの耐熱性の程度を判断する指標となるものであり、通常は、この温度が高いほど耐熱性に優れているといえる。ガラス転移温度は、示差走査熱量測定装置により、JIS-K7121に準じた方法で算出できる。 The glass transition temperature (° C.) of the aromatic polysulfone of the embodiment is preferably 200 ° C. or higher, and more preferably 215 ° C. or higher. The glass transition temperature (° C.) is an index for determining the degree of heat resistance of aromatic polysulfone, and it can be said that the higher the temperature, the better the heat resistance. The glass transition temperature can be calculated by a differential scanning calorimetry device according to JIS-K7121.
<(M)成分>
以下、ランプ部材用樹脂組成物に含有される(M)成分:長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種について説明する。
<(M) component>
Hereinafter, the component (M) contained in the resin composition for lamp members: selected from the group consisting of oxides, peroxides, compound oxides and carbon oxides of metals belonging to
長周期型周期表における1族又は2族に属する金属の酸化物としては、一般式M2 O、又はM’O(これらの式中、Mは1族、M’は2族に属する金属元素である。)で表されるものを例示できる。
長周期型周期表における1族又は2族に属する金属の過酸化物としては、一般式M’O2(これらの式中、Mは1族、M’は2族に属する金属元素である。)で表されるものを例示できる。
上記の酸化物及び過酸化物において、Mは、Na及びKからなる群から選ばれる少なくとも一種が好ましい。M’は、Mg、Ca、及びBaからなる群から選ばれる少なくとも一種が好ましく、Mg、及びCaからなる群から選ばれる少なくとも一種がより好ましく、Mgがさらに好ましい。
As the oxide of the metal belonging to
As the peroxide of the metal belonging to
In the above oxides and peroxides, M is preferably at least one selected from the group consisting of Na and K. M'is preferably at least one selected from the group consisting of Mg, Ca, and Ba, more preferably at least one selected from the group consisting of Mg, and Ca, and even more preferably Mg.
長周期型周期表における1族又は2族に属する金属を含む複酸化物とは、一般式M2O・mM’’O2・xH2O、M’O・mM’’O2・xH2O、M2O・pM’’’2O3・mM’’O2・xH2OまたはM2O・pM’OmM’’’2O3・nM’’O2・xH2O(これらの式中、Mは1族に属する金属元素、M’は2族に属する金属元素、M’’は4価の金属元素、M’’’は3価の金属元素、p,m,nは1以上の正数、xは0以上の正数)で表されるものを例示できる。
上記の複酸化物において、Mは、Kであることが好ましく、M’はMg、Ca、及びBaからなる群から選ばれる少なくとも一種であることが好ましい。この例としては、ウォラストナイト、アタパルジャイト、セリサイト、マイカ、チタン酸カリウム、チタン酸バリウムなどが挙げられるがこれらに限定されるものではない。
The compound oxide containing a metal belonging to
In the above-mentioned compound oxide, M is preferably K, and M'is preferably at least one selected from the group consisting of Mg, Ca, and Ba. Examples of this include, but are not limited to, wollastonite, attapulsite, sericite, mica, potassium titanate, barium titanate and the like.
長周期型周期表における1族又は2族に属する金属を含む炭酸塩とは、一般式M2CO3、M’CO3またはM’・M’’(CO3)2(式中、Mは1族、M’およびM’’は2族に属する金属元素)で表されるものを例示できる。
上記の炭酸塩において、MはKであることが好ましく、M’およびM’’はMg、Ca、及びBaからなる群から選ばれる少なくとも一種であることが好ましい。この例としては、炭酸カリウム、炭酸カルシウム、ドロマイトなどが挙げられるがこれらに限定されるものではない。
また、長周期型周期表における1族又は2族に属する金属を含む炭酸塩として、層状複水酸化物を例示できる。層状複水酸化物としては、ハイドロタルサイトが挙げられる。これらは、1種または2種以上を組み合わせて使用することができる。これらの中で、ハイドロタルサイトが好ましい。なお、ハイドロタルサイトは、式:
Mg1-yAly(OH)2(CO3)y/2・qH2O
[式中、0<y≦0.5、0≦qの数値を表す]
で表される。
ハイドロタルサイトは、天然物であっても、合成品であってもよく、またその結晶構造、結晶粒子径などを問わず使用することができる。
Carbonates containing metals belonging to
In the above carbonate, M is preferably K, and M'and M'is preferably at least one selected from the group consisting of Mg, Ca, and Ba. Examples of this include, but are not limited to, potassium carbonate, calcium carbonate, dolomite and the like.
Further, as a carbonate containing a metal belonging to
Mg 1-y Al y (OH ) 2 (CO 3) y / 2 · qH 2 O
[Representing numerical values of 0 <y ≦ 0.5 and 0 ≦ q in the formula]
It is represented by.
The hydrotalcite may be a natural product or a synthetic product, and can be used regardless of its crystal structure, crystal particle size, and the like.
長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物として、それらの混合物または固溶物を使用してもよい。金属酸化物の混合物または固溶物の例としては、焼成ドロマイト(酸化カルシウム及び酸化マグネシウムを含む混合物)、焼成ハイドロタルサイト(酸化カルシウムと酸化アルミニウムの固溶物)等が挙げられる。市販されている例としては、例えば、焼成ドロマイト(吉澤石灰工業社製「KT」等)、酸化カルシウム(三共精粉社製「モイストップ#10」等)、酸化マグネシウム(協和化学工業社製「キョーワマグMF-150」、「キョーワマグMF-30」、タテホ化学工業社製「ピュアマグFNMG」等)、軽焼酸化マグネシウム(タテホ化学工業社製の「#500」、「#1000」、「#5000」等)、焼成ハイドロタルサイト(戸田工業社製「N41S」、協和化学工業社製「KW-2100」、「KW-2200」等)、半焼成ハイドロタルサイト(協和化学工業社製「DHT-4C」、「DHT-4A-2」等)等が挙げられる。
As the oxides, peroxides, double oxides and carbon oxides of metals belonging to
(M)成分としては、酸性ガス(亜硫酸ガス)との中和の観点から、アルカリ性を示すものが好ましく、例えば、酸化マグネシウム、酸化カルシウム、酸化バリウム、過酸化バリウム、ウォラストナイト、アタパルジャイト、セリサイト、マイカ、チタン酸カリウム、チタン酸バリウム、炭酸カリウム、炭酸カルシウム、ドロマイト、ハイドロタルサイト、焼成ハイドロタルサイト等が好ましい。 As the component (M), those exhibiting alkalinity are preferable from the viewpoint of neutralization with acid gas (sulfite gas), and for example, magnesium oxide, calcium oxide, barium oxide, barium peroxide, wollastonite, attapulsite, and seri. Cyto, mica, potassium titanate, barium titanate, potassium carbonate, calcium carbonate, dolomite, hydrotalcite, calcined hydrotalcite and the like are preferable.
(M)成分は、1種が単独で含有されてもよく、2種類以上が組合せて含有されてもよい。 As the component (M), one type may be contained alone, or two or more types may be contained in combination.
上記に例示したもののうち、ランプの曇りの発生をより効果的に低減可能であるとの観点から、(M)成分が、長周期型周期表における1族又は2族に属する金属の酸化物であることが好ましく、(M)成分が、酸化マグネシウムであることがより好ましい。
Among those exemplified above, from the viewpoint that the occurrence of fog of the lamp can be reduced more effectively, the component (M) is an oxide of a metal belonging to
前記(M)成分の含有量は、前記(P)成分100質量部に対して、0.5~10質量部であることが好ましく、0.7~10質量部であることが好ましく、1~7質量部であることがより好ましく、1~5質量部であることがさらに好ましく、1.5~4質量部であることが特に好ましい。上記で例示した(M)成分の含有量の数値範囲の上限値と下限値とは、自由に組み合わせることができる。
(M)成分を上記下限値以上で含むランプ部材用樹脂組成物は、ランプの曇りの発生をより効果的に低減可能である。また、(M)成分を上記上限値以下で含むことにより、ランプ部材用組成物の耐熱性が良好であり、(M)成分の添加による、ランプ部材用樹脂組成物の溶融粘度の増加が生じ難く、ランプ部材用樹脂組成物の品質を安定化させ易い。
The content of the component (M) is preferably 0.5 to 10 parts by mass, preferably 0.7 to 10 parts by mass, and 1 to 1 to 10 parts by mass with respect to 100 parts by mass of the component (P). It is more preferably 7 parts by mass, further preferably 1 to 5 parts by mass, and particularly preferably 1.5 to 4 parts by mass. The upper limit value and the lower limit value of the numerical range of the content of the component (M) exemplified above can be freely combined.
The resin composition for a lamp member containing the component (M) at the above lower limit value or more can more effectively reduce the occurrence of fogging of the lamp. Further, when the component (M) is contained below the above upper limit value, the heat resistance of the composition for the lamp member is good, and the addition of the component (M) causes an increase in the melt viscosity of the resin composition for the lamp member. It is difficult to stabilize the quality of the resin composition for lamp members.
ランプ部材用樹脂組成物の上記溶融粘度としてはキャピラリーレオメーターを用いて測定された、380℃における溶融粘度を採用でき、以下に記載の測定方法により測定することができる。 As the melt viscosity of the resin composition for a lamp member, the melt viscosity at 380 ° C. measured using a capillary rheometer can be adopted, and the melt viscosity can be measured by the measurement method described below.
(ランプ部材用樹脂組成物の見かけ溶融粘度の測定)
ランプ部材用樹脂組成物の380℃における溶融粘度として、キャピラリーレオメーターを用いて測定される、380℃における溶融粘度を測定する。キャピラリーは、直径1.0mm、長さ10mmのものを用い、150℃で4時間乾燥させたペレット状のランプ部材用樹脂組成物20gを380℃に設定したシリンダーに入れ、ISO 11443に準拠し、せん断速度12000s-1における溶融粘度を測定したものとする。
(Measurement of apparent melt viscosity of resin composition for lamp members)
As the melt viscosity of the resin composition for a lamp member at 380 ° C., the melt viscosity at 380 ° C. measured using a capillary rheometer is measured. A capillary having a diameter of 1.0 mm and a length of 10 mm was used, and 20 g of a pellet-shaped resin composition for a lamp member dried at 150 ° C. for 4 hours was placed in a cylinder set at 380 ° C. and conformed to ISO 11443. It is assumed that the melt viscosity at a shear rate of 12000s- 1 has been measured.
発明者らは、上記の溶融粘度の増加の抑制は、ランプ部材用樹脂組成物に含まれる塩素(Cl)の含有量が高いほどより顕著に奏されること見出だしており、塩素(Cl)の含有量が2000質量ppm超、好ましくは3000質量ppm以上5000質量ppm以下である芳香族ポリスルホン組成物において、前記(M)成分の含有量は、前記(P)成分100質量部に対して0.5~10質量部であることが好ましく、0.7~10質量部であることが好ましく、1~7質量部であることがより好ましく、1~5質量部であることがさらに好ましく、1.5~4質量部であることが特に好ましい。上記で例示した(M)成分の含有量の数値範囲の上限値と下限値とは、自由に組み合わせることができる。 The inventors have found that the suppression of the increase in melt viscosity is more pronounced as the content of chlorine (Cl) contained in the resin composition for lamp members is higher, and the chlorine (Cl) is more pronounced. In an aromatic polysulfone composition having a content of more than 2000% by mass, preferably 3000% by mass or more and 5000% by mass or less, the content of the component (M) is 0 with respect to 100 parts by mass of the component (P). .5 to 10 parts by mass, preferably 0.7 to 10 parts by mass, more preferably 1 to 7 parts by mass, further preferably 1 to 5 parts by mass, 1 It is particularly preferably .5 to 4 parts by mass. The upper limit value and the lower limit value of the numerical range of the content of the component (M) exemplified above can be freely combined.
或いは、上記溶融粘度の増加が生じ難いとの観点から、ランプ部材用樹脂組成物に含まれる塩素(Cl)の含有量が、2000質量ppm以下であることが好ましく、1700質量ppm以下であることがより好ましく、1500質量ppm以下であることがさらに好ましい。ここでの、ランプ部材用樹脂組成物に含まれる塩素(Cl)の含有量の下限値としては、例えば、100質量ppm以上であってよく、500ppm以上であってもよい。ここでの、ランプ部材用樹脂組成物に含まれる塩素(Cl)の含有量の好ましい範囲としては、例えば、100質量ppm以上2000質量ppm以下であってよく、100質量ppm以上1700質量ppm以下であってよく、500ppm以上1500質量ppm以下であってよい。 Alternatively, from the viewpoint that the increase in melt viscosity is unlikely to occur, the content of chlorine (Cl) contained in the resin composition for lamp members is preferably 2000 mass ppm or less, and preferably 1700 mass ppm or less. Is more preferable, and 1500 mass ppm or less is further preferable. Here, the lower limit of the content of chlorine (Cl) contained in the resin composition for lamp members may be, for example, 100 ppm by mass or more, or 500 ppm or more. Here, the preferable range of the content of chlorine (Cl) contained in the resin composition for lamp members is, for example, 100 mass ppm or more and 2000 mass ppm or less, and 100 mass ppm or more and 1700 mass ppm or less. It may be 500 ppm or more and 1500 mass ppm or less.
上記のランプ部材用樹脂組成物に含まれる塩素(Cl)は、芳香族ポリスルホンが、その末端に有するCl原子と対応してよい。 Chlorine (Cl) contained in the above resin composition for lamp members may correspond to the Cl atom of the aromatic polysulfone at its terminal.
芳香族ポリスルホンは、通常、塩基及び反応溶媒の共存下で、芳香族ジハロゲノスルホン化合物と芳香族ジヒドロキシ化合物とを重縮合反応させることで製造される(例えば、特表2012-509375号公報参照)。つまり、芳香族ジハロゲノスルホン化合物と芳香族ジヒドロキシ化合物との重縮合反応によって得られる芳香族ポリスルホンは、その末端にハロゲン原子またはフェノール性水酸基を有する。 Aromatic polysulfone is usually produced by polycondensation reaction of an aromatic dihalogenosulfone compound and an aromatic dihydroxy compound in the coexistence of a base and a reaction solvent (see, for example, Japanese Patent Application Laid-Open No. 2012-509375). .. That is, the aromatic polysulfone obtained by the polycondensation reaction of the aromatic dihalogenosulfone compound and the aromatic dihydroxy compound has a halogen atom or a phenolic hydroxyl group at the terminal thereof.
ランプ部材用樹脂組成物に含まれる塩素(Cl)の含有量は、例えば、特開2018-070698号公報に開示される方法を採用することで、調整可能である。 The content of chlorine (Cl) contained in the resin composition for lamp members can be adjusted by, for example, adopting the method disclosed in Japanese Patent Application Laid-Open No. 2018-070698.
より具体的には、芳香族ジハロゲノスルホン化合物と芳香族ジヒドロキシ化合物との重縮合反応により、芳香族ポリスルホンを製造する方法において、前記重縮合反応を、少なくとも一種の芳香族末端キャップ剤の共存下で行うことが挙げられる。 More specifically, in a method for producing aromatic polysulfone by a polycondensation reaction of an aromatic dihalogenosulfone compound and an aromatic dihydroxy compound, the polycondensation reaction is carried out in the presence of at least one aromatic end cap agent. Can be mentioned in.
芳香族末端キャップ剤としては、特開2018-070698号公報に開示されるものが挙げられ、例えば、ハロゲン原子への反応性やラジカルの発生しやすい構造を含まないことや入手のしやすさの観点から4-フェニルフェノール、1-ナフトール、2-ナフトール、及び4-フェノキシフェノールが好ましい。 Examples of the aromatic terminal cap agent include those disclosed in Japanese Patent Application Laid-Open No. 2018-070698. For example, it does not contain a structure that is reactive to halogen atoms or easily generates radicals, and is easily available. From the viewpoint, 4-phenylphenol, 1-naphthol, 2-naphthol, and 4-phenoxyphenol are preferable.
前記重縮合反応を、少なくとも一種の芳香族末端キャップ剤の共存下で行い、芳香族ポリスルホンを得たのち、その溶媒を除去することや、芳香族ポリスルホンを含む析出物を、貧溶媒で繰返し洗浄すること等により、塩素(Cl)を効率的に除去することができる。 The polycondensation reaction is carried out in the coexistence of at least one aromatic terminal cap agent to obtain aromatic polysulfone, and then the solvent is removed, and the precipitate containing aromatic polysulfone is repeatedly washed with a poor solvent. By doing so, chlorine (Cl) can be efficiently removed.
発明者らは、後述の実施例に示されるように、(M)成分として、酸化マグネシウムを用いることにより、上記の溶融粘度の増加が生じ難いことを見出した。
これはおそらく、金属酸化物の添加により、末端にCl原子を有する芳香族ポリスルホンの重合反応が進行する場合があるところ、酸化マグネシウムを用いることで、このような重合反応の進行が起こり難いものと推察される。
The inventors have found that the above-mentioned increase in melt viscosity is unlikely to occur by using magnesium oxide as the component (M), as shown in Examples described later.
This is probably because the addition of a metal oxide may cause the polymerization reaction of aromatic polysulfone having a Cl atom at the end to proceed, but the use of magnesium oxide makes it difficult for such a polymerization reaction to proceed. Inferred.
したがって、ランプの曇りの発生を特に効果的に低減可能であり、さらに上記の溶融粘度の増加が生じ難いという観点から、(M)成分は、酸化マグネシウムであることが特に好ましい。
ランプ部材は比較的大型のものが多く、その成形にあたっては、組成物の適度な流動性が求められることが多い。実施形態のランプ部材用樹脂組成物において溶融粘度の増加が生じ難いことは、ランプ部材の製造に用いられる組成物として、好適な特徴であるといえる。
また、溶融粘度の増加を抑制するとの観点からも、(M)成分の含有量を上記に例示した範囲とすることが好ましい。
Therefore, it is particularly preferable that the component (M) is magnesium oxide from the viewpoint that the occurrence of fogging of the lamp can be reduced particularly effectively and the above-mentioned increase in melt viscosity is unlikely to occur.
Many of the lamp members are relatively large, and in their molding, appropriate fluidity of the composition is often required. It can be said that the fact that the melt viscosity of the resin composition for a lamp member of the embodiment is unlikely to increase is a suitable feature as a composition used for manufacturing a lamp member.
Further, from the viewpoint of suppressing an increase in the melt viscosity, it is preferable that the content of the component (M) is in the range exemplified above.
実施形態のランプ部材用樹脂組成物は、前記(P)成分の還元粘度が0.36(dL/g)超0.50(dL/g)以下であり、(M)成分が酸化マグネシウムであるものが、ランプ部材用樹脂組成物の耐熱性と、ランプの曇り発生の低減とが、より一層良好に達成され好ましい。 In the resin composition for a lamp member of the embodiment, the reduced viscosity of the component (P) is more than 0.36 (dL / g) and 0.50 (dL / g) or less, and the component (M) is magnesium oxide. It is preferable that the heat resistance of the resin composition for the lamp member and the reduction of the occurrence of fogging of the lamp are further satisfactorily achieved.
実施形態のランプ部材用樹脂組成物は、前記(P)成分の還元粘度が0.36(dL/g)超0.50(dL/g)以下であり、(M)成分が酸化マグネシウムであり、(M)成分の含有量は、前記(P)成分100質量部に対して1~10質量部であるものが、ランプ部材用樹脂組成物の耐熱性と、ランプの曇り発生の低減とが、より一層良好に達成され特に好ましい。 In the resin composition for a lamp member of the embodiment, the reduced viscosity of the component (P) is more than 0.36 (dL / g) and 0.50 (dL / g) or less, and the component (M) is magnesium oxide. The content of the component (M) is 1 to 10 parts by mass with respect to 100 parts by mass of the component (P), which improves the heat resistance of the resin composition for lamp members and reduces the occurrence of fogging of the lamp. , Even better achieved, especially preferred.
(他の成分)
本実施形態においてランプ部材用樹脂組成物は、本発明の効果を損なわない範囲において、(P)成分及び(M)成分のいずれにも該当しない、他の成分を含有してもよい。
(Other ingredients)
In the present embodiment, the resin composition for a lamp member may contain other components that do not correspond to any of the components (P) and (M) as long as the effects of the present invention are not impaired.
他の成分の例としては、充填材、添加剤、前記(P)成分以外の樹脂(以下、「その他の樹脂」ということがある。)等が挙げられる。
これら他の成分は、1種が単独で含有されてもよいし、2種以上が含有されてもよい。
Examples of other components include fillers, additives, resins other than the component (P) (hereinafter, may be referred to as “other resins”) and the like.
These other components may be contained alone or in combination of two or more.
充填材は、繊維状充填材や粒状充填材であってもよい。
また、充填材は、無機充填材であってもよいし、有機充填材であってもよい。
The filler may be a fibrous filler or a granular filler.
Further, the filler may be an inorganic filler or an organic filler.
繊維状無機充填材の例としては、ガラス繊維;パン系炭素繊維、ピッチ系炭素繊維等の炭素繊維;シリカ繊維、アルミナ繊維、シリカアルミナ繊維等のセラミック繊維;及びステンレス繊維等の金属繊維が挙げられる。また、チタン酸カリウムウイスカー、チタン酸バリウムウイスカー、ウォラストナイトウイスカー、ホウ酸アルミニウムウイスカー、窒化ケイ素ウイスカー、炭化ケイ素ウイスカー等のウイスカーも挙げられる。 Examples of the fibrous inorganic filler include glass fibers; carbon fibers such as pan-based carbon fibers and pitch-based carbon fibers; ceramic fibers such as silica fibers, alumina fibers and silica-alumina fibers; and metal fibers such as stainless steel fibers. Be done. Further, whiskers such as potassium titanate whiskers, barium titanate whiskers, wollast night whiskers, aluminum borate whiskers, silicon nitride whiskers, and silicon carbide whiskers can also be mentioned.
ガラス繊維の例としては、チョップドガラス繊維、ミルドガラス繊維等、種々の方法で製造されたものが挙げられる。 Examples of glass fibers include those manufactured by various methods such as chopped glass fibers and milled glass fibers.
炭素繊維の例としては、ポリアクリロニトリルを原料とするパン系炭素繊維、石炭タールや石油ピッチを原料とするピッチ系炭素繊維、ビスコースレーヨンや酢酸セルロース等を原料とするセルロース系炭素繊維、炭化水素等を原料とする気相成長系炭素繊維が挙げられる。炭素繊維は、チョップド炭素繊維であってもよいし、ミルド炭素繊維であってもよい。 Examples of carbon fibers include pan-based carbon fibers made from polyacrylonitrile, pitch-based carbon fibers made from coal tar and petroleum pitch, cellulose-based carbon fibers made from viscose rayon and cellulose acetate, and hydrocarbons. Examples thereof include vapor-phase growth-based carbon fibers made from rayon and the like. The carbon fiber may be chopped carbon fiber or milled carbon fiber.
粒状無機充填材の例としては、シリカ、アルミナ、酸化チタン、窒化ホウ素、炭化ケイ素及び炭酸カルシウム等が挙げられる。 Examples of granular inorganic fillers include silica, alumina, titanium oxide, boron nitride, silicon carbide, calcium carbonate and the like.
添加剤の例としては、計量安定剤、離型剤、酸化防止剤、熱安定剤、紫外線吸収剤、帯電防止剤、界面活性剤、難燃剤及び着色剤が挙げられる。 Examples of additives include metering stabilizers, mold release agents, antioxidants, heat stabilizers, UV absorbers, antistatic agents, surfactants, flame retardants and colorants.
その他の樹脂の例としては、ポリプロピレン、ポリアミド、ポリエステル、ポリフェニレンスルフィド、ポリエーテルケトン、ポリカーボネート、ポリフェニレンエーテル、ポリエーテルイミド、フッ素樹脂等の液晶ポリマー以外の熱可塑性樹脂;フェノール樹脂、エポキシ樹脂、ポリイミド樹脂、シアネート樹脂等の熱硬化性樹脂が挙げられる。 Examples of other resins include thermoplastic resins other than liquid crystal polymers such as polypropylene, polyamide, polyester, polyphenylene sulfide, polyetherketone, polycarbonate, polyphenylene ether, polyetherimide, and fluororesin; phenolic resin, epoxy resin, and polyimide resin. , Thermoplastic resins such as cyanate resin.
≪ランプ部材用樹脂組成物の製造方法≫
本実施形態のランプ部材用樹脂組成物は、(P)成分、(M)成分及び必要に応じて用いられる他の成分を、一括または適当な順序で混合することにより製造できる。
本実施形態のランプ部材用樹脂組成物の製造方法は、(P)成分と(M)成分とを混合する工程を有する。
<< Manufacturing method of resin composition for lamp members >>
The resin composition for a lamp member of the present embodiment can be produced by mixing the component (P), the component (M) and other components used as necessary in a batch or in an appropriate order.
The method for producing a resin composition for a lamp member of the present embodiment includes a step of mixing the component (P) and the component (M).
(P)成分及び(M)成分としては、上記の≪ランプ部材用樹脂組成物≫において説明したものが挙げられる。 Examples of the component (P) and the component (M) include those described in the above << Resin composition for lamp member >>.
前記(M)成分の使用量は、前記(P)成分100質量部に対して0.5~10質量部の割合で混合することが好ましく、1~7質量部の割合で混合することがより好ましく、1.5~4質量部の割合で混合することがさらに好ましい。(M)成分を上記下限値以上の割合で混合して得られたランプ部材用樹脂組成物は、ランプの曇りの発生をより効果的に低減可能である。また、(M)成分を上記上限値以下の割合で混合して得られたランプ部材用樹脂組成物では、ランプ部材用組成物の耐熱性が良好であり、(M)成分の添加による溶融粘度の増加が生じ難く、ランプ部材用樹脂組成物の品質を安定化させ易い。 The amount of the component (M) used is preferably 0.5 to 10 parts by mass with respect to 100 parts by mass of the component (P), and more preferably 1 to 7 parts by mass. It is preferable to mix in a ratio of 1.5 to 4 parts by mass, more preferably. The resin composition for a lamp member obtained by mixing the component (M) at a ratio of the lower limit value or more can more effectively reduce the occurrence of fogging of the lamp. Further, the resin composition for lamp members obtained by mixing the component (M) at a ratio of not more than the above upper limit has good heat resistance of the composition for lamp members, and the melt viscosity due to the addition of the component (M). Is unlikely to increase, and it is easy to stabilize the quality of the resin composition for lamp members.
前記混合としては、溶融混練が好ましい。本実施形態のランプ部材用樹脂組成物は、(P)成分、(M)成分および必要に応じて用いられる他の成分を、押出機を用いて溶融混練することで、ペレット化したものとして提供可能である。 As the mixing, melt kneading is preferable. The resin composition for a lamp member of the present embodiment is provided as pelletized by melting and kneading the component (P), the component (M) and other components used as necessary using an extruder. It is possible.
実施形態のランプ部材用樹脂組成物は、(M)成分:長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種を含有することで、ランプの曇りの低減効果が発揮される。
The resin composition for lamp members of the embodiment is selected from the group consisting of (M) component: oxides, peroxides, compound oxides and carbon oxides of metals belonging to
ランプ部材用樹脂組成物におけるランプの曇りの低減効果は、ランプを実際に製造せずとも確認できる。例えば、実施例に具体的に記載した方法のように、ランプを模した試験装置を用いることができ、光源を収める筐体の空間容積を想定した容器中に、ランプ部材用樹脂組成物の硬化物を収容した後、容器内を加熱して、加熱前後で容器内部に付着した成分量の比較結果や、実際の曇りの程度の比較結果を取得することができる。そして、前記(P)成分を含む樹脂組成物に比べ、該樹脂組成物にさらに(M)成分を添加して得られた実施形態に係る樹脂組成物のほうで、加熱後に容器内部に付着した成分量が低減されていること、曇りの程度が低い場合、又は曇りの発生までの加熱時間が短い場合などで、ランプの曇りの低減効果が奏されたと判断できる。 The effect of reducing fogging of the lamp in the resin composition for the lamp member can be confirmed without actually manufacturing the lamp. For example, as in the method specifically described in the examples, a test device imitating a lamp can be used, and the resin composition for a lamp member is cured in a container assuming a space volume of a housing for accommodating a light source. After storing the object, the inside of the container is heated, and the comparison result of the amount of components adhering to the inside of the container before and after heating and the comparison result of the actual degree of cloudiness can be obtained. Then, as compared with the resin composition containing the component (P), the resin composition according to the embodiment obtained by further adding the component (M) to the resin composition adhered to the inside of the container after heating. It can be determined that the effect of reducing the fogging of the lamp is achieved when the amount of the component is reduced, the degree of fogging is low, or the heating time until the occurrence of fogging is short.
(M)成分によるランプの曇りの低減効果が発揮されるメカニズムは、以下のように推察される。ランプ部材用樹脂組成物に含まれる(P)成分が加熱されると亜硫酸(SO2)ガスが発生し、例えばランプのガラスレンズに含まれるNaと反応した硫酸ナトリウムがガラスレンズに付着すると考えられる。ここに上記(M)成分を添加することで、(M)成分が亜硫酸ガスと反応し、亜硫酸ガスの発生を抑制できると考えられる。 The mechanism by which the component (M) exerts the effect of reducing the fogging of the lamp is inferred as follows. When the component (P) contained in the resin composition for a lamp member is heated, sulfurous acid (SO 2 ) gas is generated, and it is considered that, for example, sodium sulfate that has reacted with Na contained in the glass lens of the lamp adheres to the glass lens. .. It is considered that by adding the above component (M), the component (M) reacts with sulfur dioxide gas and the generation of sulfur dioxide gas can be suppressed.
以上、説明したとおり、実施形態のランプ部材用樹脂組成物は、(P)成分を含むことにより、実施形態のランプ用組成物から成形された成形体は優れた耐熱特性を発揮する。 また、実施形態のランプ部材用樹脂組成物が(M)成分を含むことにより、該組成物から成形されたランプの曇り発生を低減することができる。
さらに、(P)成分の還元粘度が、0.36(dL/g)超であることで、ランプの曇り発生の低減効果がより一層高められ、更にはランプ部材としてより好適な耐熱特性が発揮され、(P)成分の還元粘度が、0.50(dL/g)以下であることで、ランプ部材を成形するための成形特性がより良好となる。
さらに、(M)成分が、酸化マグネシウムであることで、ランプの曇り発生の低減効果が、さらに高められるとともに、ランプ部材を成形するための成形特性も良好となる。
このように、実施形態のランプ用組成物は、ランプ部材の成形に用いられる組成物として、大変に優れた特性を有するものである。
As described above, since the resin composition for the lamp member of the embodiment contains the component (P), the molded product molded from the composition for the lamp of the embodiment exhibits excellent heat resistance characteristics. Further, when the resin composition for the lamp member of the embodiment contains the component (M), it is possible to reduce the occurrence of fogging of the lamp formed from the composition.
Further, when the reduced viscosity of the component (P) is more than 0.36 (dL / g), the effect of reducing the occurrence of fogging of the lamp is further enhanced, and further, more suitable heat resistance characteristics as a lamp member are exhibited. When the reduced viscosity of the component (P) is 0.50 (dL / g) or less, the molding characteristics for molding the lamp member become better.
Further, when the component (M) is magnesium oxide, the effect of reducing the occurrence of fogging of the lamp is further enhanced, and the molding characteristics for molding the lamp member are also improved.
As described above, the composition for a lamp of the embodiment has very excellent properties as a composition used for molding a lamp member.
次に実施例を示して本発明をさらに詳細に説明するが、本発明は以下の実施例に限定されるものではない。 Next, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to the following Examples.
≪評価≫
<芳香族ポリスルホンの還元粘度の測定>
測定対象の芳香族ポリスルホン1gを、N,N-ジメチルホルムアミドに溶解させて、その容量を1dLとし、この溶液の粘度(η)を、オストワルド型粘度管を用いて、25℃で測定した。また、溶媒であるN,N-ジメチルホルムアミドの粘度(η0)を、オストワルド型粘度管を用いて、25℃で測定した。前記溶液の粘度(η)と前記溶媒の粘度(η0)から、比粘性率((η-η0)/η0)を求め、この比粘性率を、前記溶液の濃度(約1g/dL)で割ることにより、樹脂の還元粘度(dL/g)を求めた。
≪Evaluation≫
<Measurement of reducing viscosity of aromatic polysulfone>
1 g of aromatic polysulfone to be measured was dissolved in N, N-dimethylformamide to make the
<雲り試験>
ランプ部材用樹脂組成物のペレットを、射出成形機(PS40E5ASE,日精樹脂工業(株))を用い、シリンダー温度360℃、金型温度150℃にて幅64mm、長さ64mm、厚み1mmの平板状試験片を成形し、10mm角にカットし、これを試験片とした。試験片2gを、φ32mm、高さ15mmのシャーレに入れ、シャーレの上にソーダ石灰ガラスを置き、260℃に設定したホットプレート上で加熱し、ガラス上に曇りが発生するまでの時間を測定した。この時間が長いほど、曇り発生が低減されていることを意味する。
<Cloud test>
Pellets of the resin composition for lamp members are made into a flat plate with a width of 64 mm, a length of 64 mm, and a thickness of 1 mm at a cylinder temperature of 360 ° C and a mold temperature of 150 ° C using an injection molding machine (PS40E5ASE, Nissei Resin Industry Co., Ltd.). The test piece was molded and cut into 10 mm squares, which was used as the test piece. 2 g of the test piece was placed in a petri dish having a diameter of 32 mm and a height of 15 mm, soda-lime glass was placed on the petri dish, heated on a hot plate set at 260 ° C., and the time until fogging occurred on the glass was measured. .. The longer this time is, the less fogging is.
<180℃曲げ強度の測定>
ランプ部材用樹脂組成物のペレットを、射出成形機(PS40E5ASE,日精樹脂工業(株))を用い、シリンダー温度360℃、金型温度150℃にて幅12.7mm、長さ127mm、厚み6.4mmの棒状試験片を成形し、ASTM D790に準拠して、試験速度2mm/分、支点間距離100mm、圧子の先端の半径5mmにて、曲げ試験を実施することで、180℃での曲げ強度を測定した。曲げ強度の値については、3本の試験片についての結果の平均値を採用した。
<Measurement of bending strength at 180 ° C>
Using an injection molding machine (PS40E5ASE, Nissei Resin Industry Co., Ltd.), pellets of the resin composition for lamp members were subjected to a cylinder temperature of 360 ° C. and a mold temperature of 150 ° C., a width of 12.7 mm, a length of 127 mm, and a thickness of 6. A 4 mm rod-shaped test piece is formed, and a bending test is performed at a test speed of 2 mm / min, a distance between fulcrums of 100 mm, and an indenter tip radius of 5 mm in accordance with ASTM D790. Was measured. For the value of bending strength, the average value of the results for the three test pieces was adopted.
<ランプ部材用樹脂組成物の見かけ溶融粘度の測定>
ランプ部材用樹脂組成物の溶融粘度として、キャピラリーレオメーターを用いて測定された、380℃における溶融粘度を測定した。キャピラリーは1.0mmΦ×10mmを用い、150℃で4時間乾燥させたランプ部材用樹脂組成物のペレット20gを380℃に設定したシリンダーに入れ、ISO 11443に準拠し、せん断速度12000s-1における溶融粘度を測定した。
<Measurement of apparent melt viscosity of resin composition for lamp members>
As the melt viscosity of the resin composition for a lamp member, the melt viscosity at 380 ° C. measured using a capillary rheometer was measured. A capillary of 1.0 mmΦ × 10 mm was used, and 20 g of pellets of a resin composition for a lamp member dried at 150 ° C. for 4 hours was placed in a cylinder set at 380 ° C., and melted at a shear rate of 12000s -1 in accordance with ISO 11443. The viscosity was measured.
<芳香族ポリスルホンのガラス転移温度の測定>
示差走査熱量測定装置(島津製作所製DSC-50)を用い、JIS-K7121に準じた方法でガラス転移温度を算出した。サンプル約10mgを秤量し、昇温速度10℃/minで400℃まで上昇させた後、50℃まで冷却し、再び昇温速度10℃/minで400℃まで上昇させた。2回目の昇温で得られたDSCチャートより、JIS-K7121に準じた方法でガラス転移温度を算出した。
<Measurement of glass transition temperature of aromatic polysulfone>
The glass transition temperature was calculated by a method according to JIS-K7121 using a differential scanning calorimetry device (DSC-50 manufactured by Shimadzu Corporation). About 10 mg of the sample was weighed and raised to 400 ° C. at a heating rate of 10 ° C./min, cooled to 50 ° C., and again raised to 400 ° C. at a heating rate of 10 ° C./min. From the DSC chart obtained by the second temperature rise, the glass transition temperature was calculated by a method according to JIS-K7121.
≪ランプ部材用樹脂組成物の製造≫
(実施例1)
(P)成分として、スミカエクセルPES4100P(ポリエーテルスルホン(PES)、住友化学株式会社製、ガラス転移温度:225℃、還元粘度:0.41dL/g)100質量部と、(M)成分として酸化マグネシウム(協和化学工業株式会社製 キョーワマグ150)を.5質量部とを混合後、二軸押出機(PCM-30、株式会社池貝鉄工製)を用いて溶融混練することにより、ランプ部材用樹脂組成物のペレットを製造した。溶融混練条件としては、二軸押出機のシリンダー設定温度を340℃とし、スクリュー回転速度を150rpmとした。
≪Manufacturing of resin composition for lamp member≫
(Example 1)
As a component (P), 100 parts by mass of Sumika Excel PES4100P (polyether sulfone (PES), manufactured by Sumitomo Chemical Industry Co., Ltd., glass transition temperature: 225 ° C., reducing viscosity: 0.41 dL / g), and oxidation as a component (M). Magnesium (
(実施例2~12、比較例1~2)
実施例1において、PESの種類、金属酸化物の種類及びその配合量を表1に記載のとおり変更した以外は、実施例1と同様にして、ランプ部材用樹脂組成物のペレットを製造した。表中の「-」はその成分を含まないことを意味する。酸化カルシウムは、井上石灰工業株式会社製(VESTA-PP)を用いた。スミカエクセルPES3600Pは、ポリエーテルスルホン(PES)、住友化学株式会社製、ガラス転移温度:225℃、還元粘度:0.36dL/gを用いた。
(Examples 2 to 12, Comparative Examples 1 to 2)
In Example 1, pellets of the resin composition for lamp members were produced in the same manner as in Example 1 except that the type of PES, the type of metal oxide, and the blending amount thereof were changed as shown in Table 1. "-" In the table means that the component is not included. As calcium oxide, Inoue Lime Industry Co., Ltd. (VESTA-PP) was used. As the Sumika Excel PES3600P, a polyether sulfone (PES) manufactured by Sumitomo Chemical Co., Ltd., a glass transition temperature of 225 ° C., and a reduction viscosity of 0.36 dL / g were used.
製造された各ランプ部材用樹脂組成物の試験片(成形体)について、上記の曇り試験、及び180℃曲げ強度の測定をそれぞれ行った。結果を表1に併記する。 The above-mentioned fogging test and measurement of 180 ° C. bending strength were carried out for each of the manufactured test pieces (molded parts) of the resin composition for lamp members. The results are also shown in Table 1.
また、比較例1、実施例1、実施例2、実施例5及び実施例6のランプ部材用樹脂組成物について、上記の見かけ溶融粘度の測定を行った。結果を図2に示す。 Further, the above-mentioned apparent melt viscosity was measured for the resin compositions for lamp members of Comparative Example 1, Example 1, Example 2, Example 5, and Example 6. The results are shown in FIG.
表1を参照すると、(P)成分及び(M)成分を含む実施例1~10のランプ部材用樹脂組成物は、(M)成分を含まない比較例1~2のランプ部材用樹脂組成物に比べ、曇り試験での曇りの発生が抑制されていた。 Referring to Table 1, the resin compositions for lamp members of Examples 1 to 10 containing the components (P) and (M) are the resin compositions for lamp members of Comparative Examples 1 and 2 not containing the component (M). In comparison, the occurrence of fogging in the fogging test was suppressed.
また、(P)成分のPESの還元粘度が0.36(dL/g)を超える実施例1~7のランプ部材用樹脂組成物では、180℃曲げ強度の値が高く、特に優れた耐熱特性を有していた。 Further, in the resin compositions for lamp members of Examples 1 to 7 in which the reduced viscosity of PES of the component (P) exceeds 0.36 (dL / g), the value of bending strength at 180 ° C. is high, and particularly excellent heat resistance characteristics are obtained. Had.
また、実施例2と実施例8との対比、実施例4と実施例9との対比、実施例5と実施例10との対比、実施例6と実施例11との対比、実施例7と実施例12との対比によれば、(P)成分のPESの還元粘度が高いほど、曇り試験での曇りの発生が抑制されていた。 Further, comparison between Example 2 and Example 8, comparison between Example 4 and Example 9, comparison between Example 5 and Example 10, comparison between Example 6 and Example 11, and Example 7 and According to the comparison with Example 12, the higher the reduced viscosity of PES of the component (P), the more the occurrence of fogging in the fogging test was suppressed.
また、実施例2と実施例6との対比、実施例4と実施例7との対比によれば、(M)成分としてMgOを使用した場合のほうが、(M)成分としてCaOを使用した場合よりも、曇り試験での曇りの発生が抑制されていた。 Further, according to the comparison between Example 2 and Example 6 and the comparison between Example 4 and Example 7, the case where MgO is used as the component (M) is the case where CaO is used as the component (M). Rather, the occurrence of fogging in the fogging test was suppressed.
(P)成分のPESの還元粘度が0.36(dL/g)を超え、(M)成分としてMgOを使用した実施例2~4では、曇り試験での曇りの発生が特に抑制されていた。 In Examples 2 to 4 in which the reduced viscosity of PES of the component (P) exceeded 0.36 (dL / g) and MgO was used as the component (M), the occurrence of fogging in the fogging test was particularly suppressed. ..
さらに図2を参照すると、(M)成分としてMgOを使用した実施例1~2では、(M)成分としてCaOを使用した実施例5~6よりも、組成物の溶融粘度の増加が生じ難いことも判明した。 Further referring to FIG. 2, in Examples 1 and 2 in which MgO was used as the component (M), the melt viscosity of the composition was less likely to increase than in Examples 5 to 6 in which CaO was used as the component (M). It turned out that.
各実施形態における各構成及びそれらの組み合わせ等は一例であり、本発明の趣旨を逸脱しない範囲で、構成の付加、省略、置換、およびその他の変更が可能である。また、本発明は各実施形態によって限定されることはなく、請求項(クレーム)の範囲によってのみ限定される。 Each configuration in each embodiment and a combination thereof are examples, and the configuration can be added, omitted, replaced, and other changes are possible without departing from the spirit of the present invention. Moreover, the present invention is not limited to each embodiment, but is limited only to the scope of claims.
1…ランプ、3…ランプ部材、10…リフレクタ、12…光源、14…レンズ、20…レンズホルダー 1 ... Lamp, 3 ... Lamp member, 10 ... Reflector, 12 ... Light source, 14 ... Lens, 20 ... Lens holder
Claims (7)
(M)成分:長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種と、
を含有する、ランプ部材用樹脂組成物。 (P) Ingredients: Aromatic polysulfone and
Component (M): At least one selected from the group consisting of oxides, peroxides, double oxides and carbon oxides of metals belonging to Group 1 or Group 2 in the long periodic table.
A resin composition for a lamp member containing.
(M)成分:長周期型周期表における1族又は2族に属する金属の酸化物、過酸化物、複酸化物及び炭酸化物からなる群より選択される少なくとも1種と、
を混合する工程を有する、ランプ部材用樹脂組成物の製造方法。 (P) Ingredients: Aromatic polysulfone and
Component (M): At least one selected from the group consisting of oxides, peroxides, double oxides and carbon oxides of metals belonging to Group 1 or Group 2 in the long periodic table.
A method for producing a resin composition for a lamp member, which comprises a step of mixing.
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| CN106810804A (en) * | 2016-12-09 | 2017-06-09 | 芜湖天鸿汽车零部件有限公司 | A kind of automobile lampshade moulding material and preparation method thereof |
| JP2018517045A (en) * | 2015-06-10 | 2018-06-28 | ソルベイ スペシャルティ ポリマーズ ユーエスエー, エルエルシー | Polymer compositions and sterilizable articles obtainable therefrom |
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- 2020-09-28 WO PCT/JP2020/036535 patent/WO2021065767A1/en not_active Ceased
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|---|---|---|---|---|
| JPH02281502A (en) * | 1989-03-22 | 1990-11-19 | Basf Ag | Polyaryl ether sulfone for lighting engineering purpose |
| JPH0834853A (en) * | 1994-03-18 | 1996-02-06 | Sekisui Chem Co Ltd | Optical materials |
| JPH1196817A (en) * | 1997-09-19 | 1999-04-09 | Sumitomo Chem Co Ltd | Lamp reflector |
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| CN106810804A (en) * | 2016-12-09 | 2017-06-09 | 芜湖天鸿汽车零部件有限公司 | A kind of automobile lampshade moulding material and preparation method thereof |
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| JPWO2021065767A1 (en) | 2021-04-08 |
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