WO2017216827A1 - Récipient stratifié moulé par soufflage résistant aux produits chimiques de faible quantité d'élution de microparticules impures - Google Patents

Récipient stratifié moulé par soufflage résistant aux produits chimiques de faible quantité d'élution de microparticules impures Download PDF

Info

Publication number
WO2017216827A1
WO2017216827A1 PCT/JP2016/002928 JP2016002928W WO2017216827A1 WO 2017216827 A1 WO2017216827 A1 WO 2017216827A1 JP 2016002928 W JP2016002928 W JP 2016002928W WO 2017216827 A1 WO2017216827 A1 WO 2017216827A1
Authority
WO
WIPO (PCT)
Prior art keywords
less
layer
resin
container
adhesive
Prior art date
Application number
PCT/JP2016/002928
Other languages
English (en)
Japanese (ja)
Inventor
小林　玄明
初夫 松尾
Original Assignee
コダマ樹脂工業株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by コダマ樹脂工業株式会社 filed Critical コダマ樹脂工業株式会社
Priority to JP2018522901A priority Critical patent/JP6518840B2/ja
Priority to CN201680086864.7A priority patent/CN109311553B/zh
Priority to KR1020197001662A priority patent/KR102192237B1/ko
Priority to PCT/JP2016/002928 priority patent/WO2017216827A1/fr
Publication of WO2017216827A1 publication Critical patent/WO2017216827A1/fr

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B1/00—Layered products having a non-planar shape
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/34—Layered products comprising a layer of synthetic resin comprising polyamides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D1/00—Containers having bodies formed in one piece, e.g. by casting metallic material, by moulding plastics, by blowing vitreous material, by throwing ceramic material, by moulding pulped fibrous material, by deep-drawing operations performed on sheet material
    • B65D1/02—Bottles or similar containers with necks or like restricted apertures, designed for pouring contents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38—Packaging materials of special type or form
    • B65D65/40—Applications of laminates for particular packaging purposes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/40—Properties of the layers or laminate having particular optical properties
    • B32B2307/402—Coloured
    • B32B2307/4026—Coloured within the layer by addition of a colorant, e.g. pigments, dyes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/714—Inert, i.e. inert to chemical degradation, corrosion
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/724—Permeability to gases, adsorption
    • B32B2307/7242—Non-permeable
    • B32B2307/7244—Oxygen barrier
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00—Containers; Receptacles

Definitions

  • the present invention relates to a chemical-resistant blow-molded laminated container with a small amount of impure particulate elution, and more specifically, excellent in chemical resistance and mechanical strength.
  • the present invention relates to a chemical-resistant blow-molded laminated container with a small amount of impure fine particles that can be used as an ultra-high-purity chemical container with no visibility.
  • plastic containers such as glass containers and sealer bottles (commercially available fragrance containers) and containers coated with the inner surface of metal containers are used as containers for storing chemicals and fragrances.
  • a glass container is inconvenient to handle because it is heavy, and may be broken by dropping.
  • a molded container made of polyethylene resin has the advantage that it is difficult to break during handling and is lightweight.
  • high-purity chemicals used for etching and cleaning in semiconductor manufacturing such as sulfuric acid, nitric acid, hydrogen peroxide water, and high-purity solvent-based resists and dilution solvents used for semiconductor processes and liquid crystal displays,
  • high-purity chemicals used for etching and cleaning in semiconductor manufacturing such as sulfuric acid, nitric acid, hydrogen peroxide water, and high-purity solvent-based resists and dilution solvents used for semiconductor processes and liquid crystal displays
  • methyl alcohol, ethyl alcohol, isopropyl alcohol, isobutyl alcohol, ethylene glycol, acetone, ethyl acetate, toluene, dimethylformamide, ethylene glycol acetate, methoxypropyl acetate, butyl cellosolve, etc. and used for pharmaceuticals such as sterilization, disinfection, and drug substance
  • High purity solvents such
  • the impure fine particles are leached from the resin composition forming the container into the chemical that is the content, and the degree to which the impure fine particles impair the content is indicated.
  • the degree of cleanness is that after molding a test container and storing ultrapure water in the test container for a certain period (30 days at 23 ° C.), the particle size is 0.2 ⁇ m or more in 1 ml of water stored in the resin container. Calculate how many fine particles there are.
  • Measuring apparatus A particle counter “KL-26” RION KL-26 manufactured by Rion Co., Ltd. is used.
  • Sample to be measured An ultrapure water filled in a molded container, stored at 23 ° C. for 30 days, and collected from a container left standing for 20 minutes in an upright state is used as a sample to be measured.
  • the particle counter Prior to measurement, the particle counter is purged with ultrapure water, and then the measuring device is washed twice with 25 ml of ultrapure water. 4). After washing, ultrapure water is injected into a 10 ml particle counter and the number of particles is measured.
  • This operation is performed twice to confirm that the number of particles of 0.2 ⁇ m or more is zero (A). 5.
  • the measuring device is washed twice with a 25 ml measuring sample. 6). After washing, 10 ml is injected into a particle counter from a container (bottle) filled with ultrapure water as a measurement sample, and the number of particles is measured. This operation is performed twice to obtain an average value (B) of the number of particles of 0.2 ⁇ m or more. 7).
  • the particle value in 1 ml is calculated from the measured value by the following formula.
  • Elution amount of impure fine particles of 2 ⁇ m or more is 5 or less, and elution amount of impure fine particles having a particle size of 0.2 ⁇ m or more in 1 ml of ultrapure water after 30 days storage at 40 ° C. ml) is required to be 10 or less.
  • Cans and sealer bottles with fluorine coating on the inner surface of metal cans are used on the market as containers used in the perfume field, but in the case of metal cans, there are problems of dents and rust. The problem of quality deterioration as a fragrance frequently occurs.
  • the weight average molecular weight of the raw material resin made of polyethylene or ethylene- ⁇ -olefin copolymer is in a certain range
  • the content of the light-shielding pigment and the dispersant in the resin composition is in a certain range
  • the resin composition A container molded from a resin composition composed of polyethylene or ethylene- ⁇ -olefin copolymer with a low molecular weight polymer and additive content less than a certain weight in the product is excellent in mechanical strength and easy to handle. It has been proposed as a light-shielding container for high-purity chemicals having a light-shielding property (see Patent Document 1), which is easy and has very little leaching of impure fine particles into stored and stored chemicals.
  • this container satisfies the cleanliness of less than 500 / ml according to the conventional measurement method, but does not become less than 5 / ml, and has an oxygen barrier property to prevent alteration of the contained liquid. There was a problem such as not having.
  • At least the inner surface of the resin is made of a resin of polyethylene or ethylene- ⁇ -olefin copolymer having a density of 940 to 970 Kg / m 3, and the neutralizing agent, antioxidant and light-resistant stabilizer in the resin are quantified by liquid chromatography.
  • the content is 0.01% by weight or less with respect to the total weight of the resin, and the resin has a weight average molecular weight of 120,000 to 260,000 as measured by gel permeation chromatography. Minute High purity solvent containers amount 1,000 of the polymer is less than 2.5% by weight relative to the total weight of the resin (see Patent Document 2) are proposed.
  • the high purity solvent container of Patent Document 2 satisfies the cleanliness of less than 500 / ml by the conventional measurement method, but the cleanliness does not become less than 5 / ml and prevents the contained liquid content from being altered. There is a problem that it is inferior in ultraviolet blocking ability.
  • a polyethylene or ethylene- ⁇ -olefin copolymer resin having a density of 940 to 970 kg / m 3, at least 0.01 wt% to 5 wt% of a light-shielding pigment such as titanium oxide or carbon black, and a liquid or gas barrier resin
  • a high-purity chemical container comprising a resin composition to which 4 to 25% by weight of the resin is added, wherein the resin has a weight average molecular weight of 120,000 to 260,000 as measured by gel permeation chromatography, A polymer having a weight average molecular weight of 1,000 or less is less than 5% by weight of the resin, and the ⁇ -olefin is selected from propylene, butene-1,4-methyl-pentene-1, hexene-1 and octene-1. At least one kind of high-purity chemical container (see Patent Document 3) has been proposed.
  • Patent Document 3 still satisfies the cleanliness of less than 500 / ml by the conventional measurement method, and has a problem that the cleanliness does not fall below 5 / ml.
  • Solvents containing poly (ethylene-co-vinyl alcohol) and an inner layer made of a high-purity resin containing various types of neutralizing agents, antioxidants, and light stabilizers at a maximum content of 0.01% by weight A container in which an intermediate layer of a barrier resin and an outer layer made of a resin composition containing a light-shielding substance are blow-molded, and the minimum absorbance at a wavelength of 400 nm or less of all layers of the container measured by a spectrophotometer is 2.
  • the absorption coefficient at a wavelength of 400 nm obtained by dividing the absorbance of all layers of the container by the thickness of the entire layer is not less than 1.5 mm ⁇ 1 and also at a wavelength of 600 nm.
  • High purity chemicals liquid container see Patent Document 4 it has been proposed, wherein the extinction coefficient is 1.5 mm-1 or less.
  • the high-purity chemical solution container of Patent Document 4 satisfies the cleanliness of less than 100 / ml by the conventional measurement method, and has a problem that the cleanliness does not become 5 / ml or less.
  • the applicant of the present invention firstly sprays an ultra-high-purity chemical obtained by laminating at least an inner layer having the following characteristics, an oxygen barrier layer containing polyvinyl alcohol resin, and an outer layer containing a light-shielding pigment in order from the inside to the outside of the container.
  • a molded laminated container having a visible light transmittance of 1% or less at a wavelength of 500 to 800 nm and an ultraviolet transmittance of a wavelength of 200 to 400 nm of 1% or less, and entering the stored chemical from the container side.
  • Inner layer high density having the following characteristics comprising a homopolymer or copolymer containing at least one selected from ethylene, propylene, butene-1,4-methyl-pentene-1, hexene-1 and octene-1 Polyolefin resin.
  • Patent Literature 1 Japanese Patent No. 2805723
  • Patent Literature 2 Japanese Patent No. 2749513
  • Patent Literature 3 Japanese Patent No. 2805188
  • Patent Literature 4 Japanese Patent No. 4167745
  • Patent Literature 5 Japanese Patent Application No. 2015-234798
  • a test container is molded, and the test container is filled with ultrapure water and filled in 1 ml of ultrapure water after being stored at 23 ° C. for 30 days.
  • the chemical-resistant blow-molded laminated container (see Patent Document 5) is excellent in chemical resistance and mechanical strength.
  • the object of the present invention is excellent in chemical resistance, mechanical strength, etc., and the cleanliness as an index indicating the number of impure fine particles leached from the container side into ultra-high purity chemicals stored and stored is 23 ° C. 5 or less after storage for 30 days and 10 or less after storage at 40 ° C. for 30 days, and has excellent oxygen barrier properties, and has a transmittance of 1% for visible light having a wavelength of 500 to 800 nm. Visibility of contents that can be used as ultra-high-purity chemical containers such as fragrances and photoresist liquids. It is an object of the present invention to provide a chemical-resistant blow-molded laminated container having a small amount of impure fine particles that are not dissolved.
  • the present inventors have intensively studied, for example, in order from the inner side to the outer side of the container, the inner layer 1, the inner layer 2, the barrier / adhesive resin layer, the adhesive layer, the barrier layer, and the outer layer.
  • the inner layer 1 does not have an adhesive functional group, has an adhesive property to the fluororesin of the inner layer 2, but has an adhesive property to other layers.
  • Additive-free heat loss without additives is 0.20% by mass or less, and the inner layer 2 has an adhesive functional group, the inner layer 1 fluororesin and the barrier / adhesive resin layer Additives containing additives and lubricants that are intentionally added as a barrier / adhesive resin layer using a specific fluororesin having an adhesive-free heat loss of 0.40% by mass or less. Do not use polyamide resin
  • the impure fine particle elution amount (number / ml) after storage at 23 ° C. for 30 days is 5 or less
  • the impure fine particle elution amount (number / ml) after storage at 40 ° C. for 30 days is 10 or less.
  • an ethylene vinyl alcohol copolymer resin By using an ethylene vinyl alcohol copolymer resin, it is possible to improve gas barrier properties, excellent in UV blocking properties and visible light blocking properties, and by using an ultra high molecular weight high density polyethylene resin having a high melt tension, drawdown, etc. Since the moldability and mechanical strength are improved, the visibility of contents that can be used as containers for ultra-high-purity chemicals that contain a lot of expensive and dangerous chemicals such as fragrances and photoresist solutions The present inventors have found that a chemical-resistant blow-molded laminated container with a small amount of impure fine particles eluted can be obtained, and the present invention has been achieved.
  • the invention of claim 1 of the present invention for solving the above-mentioned problem is to laminate the following inner layer 1, inner layer 2, barrier / adhesive resin layer, adhesive layer, barrier layer and outer layer 1 in order from the inside to the outside of the container.
  • a chemical-resistant blow-molded laminated container having a visible light transmittance of 500 to 800 nm of 1% or less and an ultraviolet transmittance of 200 to 400 nm of 1% or less at 23 ° C.
  • Impure particulate elution amount (number / ml) after storage for 30 days is 5 or less
  • impure particulate elution amount (number / ml) after storage for 30 days at 40 ° C. is 10 or less.
  • This is a chemical-resistant blow-molded laminated container with a low content.
  • Inner layer 1 is an additive-free fluororesin that has no adhesive functional group, has adhesiveness to the fluororesin of the inner layer 2 but has no adhesiveness to other layers, and has 0 weight loss on heating. 20% by mass or less.
  • Inner layer 2 An additive-free fluororesin having an adhesive functional group and adhesiveness to the fluororesin and barrier / adhesive resin layer of the inner layer 1, and having a loss on heating of 0.40% by mass or less.
  • Barrier / adhesive resin layer At least one polyamide selected from the group consisting of polyamides obtained by ring-opening polycondensation of caprolactam, which does not contain additives that are intentionally added or lubricants.
  • Adhesive layer a maleic anhydride-modified polyolefin resin.
  • Barrier layer an ethylene vinyl alcohol copolymer resin.
  • Outer layer 1 an ultra high molecular weight high density polyethylene resin that includes a light shielding pigment and a maleic anhydride-modified polyolefin resin and is excellent in adhesion to the barrier layer.
  • the invention of claim 2 of the present invention is formed by laminating the following inner layer 1, inner layer 2, barrier / adhesive resin layer, adhesive layer, barrier layer, adhesive layer and outer layer 2 in order from the inside to the outside of the container.
  • a chemical-resistant blow-molded layered container that has a visible light transmittance of 1% or less at a wavelength of 500 to 800 nm, an ultraviolet transmittance of a wavelength of 200 to 400 nm of 1% or less, and is stored at 23 ° C. for 30 days.
  • the impure fine particle elution amount (number / ml) is 5 or less
  • the impure fine particle elution amount (number / ml) after storage at 40 ° C. for 30 days is 10 or less. It is a chemical blow molded laminated container.
  • Inner layer 1 is an additive-free fluororesin that has no adhesive functional group, has adhesiveness to the fluororesin of the inner layer 2 but has no adhesiveness to other layers, and has 0 weight loss on heating. 20% by mass or less.
  • Inner layer 2 An additive-free fluororesin having an adhesive functional group and adhesiveness to the fluororesin and barrier / adhesive resin layer of the inner layer 1, and having a loss on heating of 0.40% by mass or less.
  • Barrier / adhesive resin layer At least one polyamide selected from the group consisting of polyamides obtained by ring-opening polycondensation of caprolactam, which does not contain additives that are intentionally added or lubricants.
  • Adhesive layer a maleic anhydride-modified polyolefin resin.
  • Barrier layer an ethylene vinyl alcohol copolymer resin.
  • Adhesive layer a maleic anhydride-modified polyolefin resin.
  • Outer layer 2 Ultra high molecular weight high density polyethylene resin containing light blocking pigment
  • the invention according to claim 3 of the present invention is the chemical resistant blow-molded laminated container according to claim 1 or 2, wherein the fluororesin used for the inner layer 2 is tetrafluoroethylene / hexafluoropropylene / monomer.
  • ( ⁇ ) copolymer tetrafluoroethylene / perfluoro (alkyl vinyl ether) / monomer ( ⁇ ) copolymer, ethylene / tetrafluoroethylene / monomer ( ⁇ ) copolymer, ethylene / tetrafluoroethylene / Hexafluoropropylene / monomer ( ⁇ ) copolymer, chlorotrifluoroethylene / monomer ( ⁇ ) copolymer, chlorotrifluoroethylene / tetrafluoroethylene / monomer ( ⁇ ) copolymer, and ethylene / Chlorotrifluoroethylene / monomer ( ⁇ ) copolymer is at least one selected from the group consisting of copolymers, and the monomer ( ⁇ ) is a monomer having an adhesive functional group. And a fluororesin having the following characteristics.
  • the invention according to claim 4 of the present invention is the chemical resistant blow molded laminated container according to any one of claims 1 to 3, wherein the fluororesin used for the inner layer 1 is the adhesive functional group. It is characterized by being a fluororesin having the following characteristics.
  • the invention of claim 5 of the present invention is characterized in that, in the chemical-resistant blow-molded laminated container of any one of claims 1 to 4, the polyamide resin has the following characteristics.
  • the invention according to claim 6 of the present invention is the chemical resistant blow-molded laminated container according to any one of claims 1 to 5, wherein the barrier layer is ethylene having excellent oxygen barrier properties having the following characteristics: It is a vinyl alcohol copolymer resin.
  • the invention according to claim 7 of the present invention is the chemical resistant blow molded laminated container according to claim 1, wherein the outer layer 1 is made of polyethylene or ethylene- ⁇ -olefin copolymer having the following characteristics.
  • High density polyethylene resin organic light-shielding pigments such as quinacridone, phthalocyanine, anthraquinone, monoazo, etc., carbon black, iron oxide, zinc oxide, ultramarine blue
  • the invention according to claim 8 of the present invention is the chemical resistant blow molded laminated container according to claim 2, wherein the outer layer 2 is made of polyethylene or ethylene- ⁇ -olefin copolymer having the following characteristics.
  • High density polyethylene resin organic light-shielding pigments such as quinacridone, phthalocyanine, anthraquinone, monoazo, etc., carbon black, iron oxide, zinc oxide, ultramarine blue
  • 0.05 to 0.30 mass% visible light transmittance at a wavelength of 500 to 800 nm is 1% or less, and a wavelength of 200 to 400 nm Wherein the external line transmission is composed of the composition 2 is 1% or less.
  • the invention of claim 1 of the present invention is a chemical-resistant spray comprising a laminate of the inner layer 1, inner layer 2, barrier / adhesive resin layer, adhesive layer, barrier layer and outer layer 1 in this order from the inside to the outside of the container.
  • Impregnated fine particle container having a visible light transmittance of 500 to 800 nm of 1% or less, an ultraviolet transmittance of 200 to 400 nm of wavelength of 1% or less, and stored at 23 ° C. for 30 days
  • the inner layer 1 does not have an adhesive functional group, and the fluororesin of the inner layer 2 has adhesiveness but does not have adhesiveness to other layers.
  • a specific fluororesin is used, and the inner layer 2 has an adhesive functional group, and has an adhesive-free functional heating loss of 0.40% by mass.
  • the cleanliness is 30 ° C. at 30 ° C. It is 5 or less after day storage and 10 or less after storage at 40 ° C. for 30 days, a cleanness equivalent to a glass bottle can be obtained, chemical resistance can be improved, and alteration of odor components can be reduced as much as possible. Prominent effect That.
  • the oxygen barrier properties are improved, while the fluororesin, polyamide resin, and adhesive resin are melted and the melt tension is lowered at a stretch.
  • problems such as draw-down occur in blow molding.
  • the outer layer 1 has melt tension.
  • Use of ultra-high molecular weight high-density polyethylene resin with excellent UV blocking properties, visible light blocking properties, and mechanical strength improves moldability and UV blocking properties, so it is expensive and dangerous for fragrances and photoresist solutions.
  • the chemical-resistant blow-molded laminated container of the present invention includes a maleic anhydride-modified polyolefin resin as the outer layer 1 and uses an outer layer excellent in adhesiveness with the barrier layer, the outer layer 1 and the barrier layer There is no need to provide an adhesive layer (maleic anhydride-modified polyolefin resin) between them, and there is a remarkable effect that workability and economy are further improved.
  • the chemical-resistant blow-molded laminated container of the present invention is heavy, easily damaged, and unlike a glass bottle that lacks safety, is not easily damaged, has excellent mechanical strength, and has a barrier layer. Oxygen barrier property is improved by the above, so it can be used as a perfume bottle, etc., and it can be used safely and safely as a versatile plastic container that can be used for various other contents. There is a remarkable effect of being able to. Since the chemical-resistant blow molded laminated container of the present invention has the above-mentioned characteristics, it is easy for the environment and health, contributes to environmental problems and health problems, and is economical because it also reduces costs. There is a remarkable effect of being.
  • the invention of claim 2 of the present invention is formed by laminating the inner layer 1, the inner layer 2, the barrier / adhesive resin layer, the adhesive layer, the barrier layer, the adhesive layer and the outer layer 2 in this order from the inside to the outside of the container.
  • a chemical-resistant blow-molded layered container that has a visible light transmittance of 1% or less at a wavelength of 500 to 800 nm, an ultraviolet transmittance of a wavelength of 200 to 400 nm of 1% or less, and is stored at 23 ° C. for 30 days.
  • the impure fine particle elution amount (number / ml) is 5 or less
  • the impure fine particle elution amount (number / ml) after storage at 40 ° C. for 30 days is 10 or less.
  • a chemical blow-molded laminated container The chemical-resistant blow-molded laminated container according to claim 2 of the present invention is economically acceptable because an adhesive layer (maleic anhydride-modified polyolefin resin) is provided between the outer layer 2 and the barrier layer.
  • an adhesive layer maleic anhydride-modified polyolefin resin
  • the adhesiveness between the two is ensured, it is used depending on the purpose and purpose. Except for this point, it has the same configuration as the chemical-resistant blow-molded laminated container of claim 1 of the present invention.
  • the effect and effect are the same as those of the chemical-resistant blow-molded laminated container of claim 1 of the present invention.
  • the invention according to claim 3 of the present invention is the chemical resistant blow-molded laminated container according to claim 1 or 2, wherein the fluororesin used for the inner layer 2 is tetrafluoroethylene / hexafluoropropylene / monomer.
  • ( ⁇ ) copolymer tetrafluoroethylene / perfluoro (alkyl vinyl ether) / monomer ( ⁇ ) copolymer, ethylene / tetrafluoroethylene / monomer ( ⁇ ) copolymer, ethylene / tetrafluoroethylene / Hexafluoropropylene / monomer ( ⁇ ) copolymer, chlorotrifluoroethylene / monomer ( ⁇ ) copolymer, chlorotrifluoroethylene / tetrafluoroethylene / monomer ( ⁇ ) copolymer, and ethylene / Chlorotrifluoroethylene / monomer ( ⁇ ) copolymer is at least one selected from the group consisting of copolymers, and the monomer ( ⁇ ) is a monomer having an adhesive functional group.
  • the invention of claim 4 of the present invention is the chemical resistant blow molded laminated container according to any one of claims 1 to 3, wherein the fluororesin used for the inner layer 1 has the adhesive functional group.
  • it is characterized by being a fluororesin having the above-mentioned characteristics, and it has excellent adhesiveness to the fluororesin of the inner layer 2 and can be coextruded at a molding temperature comparable to polyolefin. Has a remarkable effect.
  • the invention of claim 5 of the present invention is the chemical-resistant blow-molded laminated container according to any one of claims 1 to 4, wherein the polyamide resin has the above characteristics. And By improving the adhesion of the inner layer 2 with the fluororesin and making it free of additives and lubricants, the amount of impure particles eluted due to the additives can be greatly reduced, and a cleanliness equivalent to a glass bottle can be obtained. There is a further remarkable effect.
  • the invention according to claim 6 of the present invention is the chemical-resistant blow-molded laminated container according to any one of claims 1 to 5, wherein the barrier layer is excellent in oxygen barrier properties having the above characteristics. It is characterized by being an ethylene vinyl alcohol copolymer resin, There is a further remarkable effect that the oxygen barrier property is surely further improved.
  • the invention according to claim 7 of the present invention is the chemical resistant blow-molded laminated container according to claim 1, wherein the outer layer 1 is made of polyethylene or ethylene- ⁇ -olefin copolymer having the above characteristics.
  • High density polyethylene resin organic light-shielding pigments such as quinacridone, phthalocyanine, anthraquinone, monoazo, etc., carbon black, iron oxide, zinc oxide, ultramarine blue
  • Transmittance of light is less than 1%, which is characterized in that ultraviolet transmittance at a wavelength 200 ⁇ 400 nm is composed of the composition 1 is 1% or less, Fluorine resin, polyamide resin, and adhesive resin are melted and the melt tension drops at a stretch, causing problems such as draw-down in blow molding. For example, a uniform-thick container cannot be molded or defective products are generated.
  • the use of an ultra-high molecular weight high density polyethylene resin having a large weight average molecular weight and high melt tension for the outer layer 1 eliminates problems such as drawdown and improves moldability and mechanical strength. Improved, By using an appropriate amount of the light-shielding pigment, the visible light blocking property and the ultraviolet blocking property are surely improved, the visible light transmittance at a wavelength of 500 to 800 nm is surely 1% or less, and the ultraviolet transmittance at a wavelength of 200 to 400 nm is ensured.
  • 1% or less can be achieved, and it is a chemical-resistant blow-molded laminated container with a small amount of impure fine particles that can be used as a container for ultra-high-purity chemicals that contain a lot of expensive and dangerous chemicals such as fragrances and photoresist solutions.
  • the antioxidant in the above range the resin can be prevented from being burnt, and the physical properties and the appearance can be prevented from being deteriorated due to the burnt resin.
  • the chemical-resistant blow-molded laminated container of the present invention includes a maleic anhydride-modified polyolefin resin as the outer layer 1 and uses an outer layer excellent in adhesiveness with the barrier layer, so that the outer layer 1 and the barrier layer There is no need to provide an adhesive layer (maleic anhydride-modified polyolefin resin) between them, and there is a further remarkable effect that workability and economy are further improved.
  • the chemical-resistant blow-molded laminated container of the present invention is heavy, easily damaged, and unlike a glass bottle that lacks safety, is not easily damaged, has excellent mechanical strength, and has a barrier layer. Oxygen barrier properties are improved by this, so it can be used as a perfume bottle and can be used safely and safely as a versatile plastic container that can be used for various other contents. , Has a further remarkable effect.
  • the invention according to claim 8 of the present invention is the chemical resistant blow molded laminated container according to claim 2, wherein the outer layer 2 is made of polyethylene or ethylene- ⁇ -olefin copolymer having the following characteristics.
  • High density polyethylene resin organic light-shielding pigments such as quinacridone, phthalocyanine, anthraquinone, monoazo, etc., carbon black, iron oxide, zinc oxide, ultramarine blue
  • Visible light having a wavelength of 500 to 800 nm containing 0.05 to 0.30% by mass is 1% or less and purple having a wavelength of 200 to 400 nm
  • the linear transmittance is constituted from a composition 2 is 1% or less
  • the visible light blocking property and the ultraviolet blocking property are surely improved, the visible light transmittance at a wavelength of 500 to 800 nm is surely 1% or less, and the ultraviolet light transmission at a wavelength of 200 to 400 nm is performed.
  • the chemical-resistant blow-molded laminated container of the present invention is heavy, easy to break, hard to break, has excellent mechanical strength, and has a barrier layer compared to a glass bottle lacking safety. Oxygen barrier properties are improved by this, so it can be used as a perfume bottle and can be used safely and safely as a versatile plastic container that can be used for various other contents. This has a further remarkable effect.
  • FIG. 1 is an explanatory view illustrating a cross section of an example of a chemical-resistant blow-molded laminated container of the present invention.
  • 1A of the chemical resistant blow-molded laminated container 8A of the present invention consists of the fluororesin having no adhesive functional group, and the inner layers 1 and 1B made of the fluororesin having adhesive functional group.
  • Inner layers 2 and 2 are barrier / adhesive resin layers made of the polyamide resin
  • 3 is an adhesive layer made of maleic anhydride-modified polyolefin resin
  • 4 is a barrier layer made of ethylene vinyl alcohol copolymer resin
  • 5 is Adhesive layer 6A comprising maleic anhydride-modified polyolefin resin, ultra high molecular weight high density polyethylene having a visible light transmittance of 1% or less at a wavelength of 500-800 nm and an ultraviolet transmittance of 200% to 400 nm of 1% or less
  • Each of the outer layers 2 made of resin is shown.
  • 7 shows the ultra-high purity chemical as the contents.
  • FIG. 2 is an explanatory view illustrating a cross section of another example of the chemical-resistant blow-molded laminated container of the present invention.
  • 1A of the chemical resistant blow molded laminated container 8B of the present invention is composed of the fluororesin having no adhesive functional group, and the inner layer 1 and 1B made of the fluororesin having adhesive functional group.
  • Inner layers 2 and 2 are barrier / adhesive resin layers made of the polyamide resin
  • 3 is an adhesive layer made of maleic anhydride-modified polyolefin resin
  • 4 is a barrier layer made of ethylene vinyl alcohol copolymer resin
  • 6B is Ultra-high molecular weight comprising maleic anhydride-modified polyolefin resin having excellent adhesiveness to the barrier layer 4 and having visible light transmittance of 1% or less at a wavelength of 500 to 800 nm and ultraviolet transmittance of wavelength of 200 to 400 nm of 1% or less
  • the outer layers 1 made of high-density polyethylene resin are shown respectively.
  • 7 shows the ultra-high purity chemical as the contents.
  • the outer layer 1 contains 25 to 65% by mass of a maleic anhydride-modified polyolefin resin, the outer layer 1 has excellent adhesion between the outer layer 1 and the barrier layer 4, and has no problems such as drawdown, moldability and mechanical properties. Excellent strength.
  • the maleic anhydride-modified polyolefin resin is less than 25% by mass, the adhesion between the outer layer 1 and the barrier layer 4 may be insufficient, and if the maleic anhydride-modified polyolefin resin exceeds 65% by mass, the drawdown may occur. Such problems may occur.
  • the fluororesin used for the inner layer 2 is not particularly limited, but specifically, for example, tetrafluoroethylene / hexafluoropropylene / monomer ( ⁇ ) copolymer, tetrafluoroethylene / perfluoro (Alkyl vinyl ether) / monomer ( ⁇ ) copolymer, ethylene / tetrafluoroethylene / monomer ( ⁇ ) copolymer, ethylene / tetrafluoroethylene / hexafluoropropylene / monomer ( ⁇ ) copolymer , Chlorotrifluoroethylene / monomer ( ⁇ ) copolymer, chlorotrifluoroethylene / tetrafluoroethylene / monomer ( ⁇ ) copolymer, and ethylene / chlorotrifluoroethylene / monomer ( ⁇ ) copolymer When it is a fluororesin that is at least one selected from the group consisting of polymers and copolymerized with the mono
  • the fluororesin used for the inner layer 1 in the present invention is a fluororesin that does not copolymerize the monomer ( ⁇ ) having an adhesive functional group and does not have the adhesive functional group, and is free of additives. It is preferable to use an additive grade fluororesin.
  • the fluororesin used for the inner layer 1 has a heat loss measured by the following heat loss measurement method of 0.20% by mass or less, preferably 0.15 or less, and the fluororesin used for the inner layer 2 is the same measurement. It is necessary that the loss on heating measured by the method is 0.40% by mass or less, preferably 0.30 or less. If it is within this range, it is possible to achieve 5 or less after storage at 23 ° C. for 30 days and 10 or less after storage at 40 ° C. for 30 days. is there.
  • MFR (265 ° C., 5 kg load g / 10 min) (measuring method: 265 ° C., ASTM D1238) is preferably 10 to 40, more preferably 20 to 30. If it is less than 10, the melt viscosity is high, and the blow melt moldability is high. There is a possibility that the drive energy will be worsened, and if it exceeds 40, the melt tension is low and problems such as draw-down may occur during blow molding.
  • the specific gravity may be a commercially available specific gravity of 1.7 to 1.9, more preferably 1.72 to 1.76. If the specific gravity is less than 1.7, there is a concern that the adhesiveness may be lowered, and if it exceeds 1.9, the strength of the container may be insufficient.
  • the melting point (° C.) (measurement method: ASTM D792) varies depending on the amount and type of the monomer ( ⁇ ) to be copolymerized, but may be a melting point of 150 to 200 ° C. of a commercially available product. The temperature is preferably 190 to 200 ° C. If the melting point is less than 150 ° C., a difference in melting point from other resins may occur, which may cause problems of adhesive strength and moldability. If the melting point exceeds 200 ° C., it may be difficult to laminate with other resins. .
  • the monomer ( ⁇ ) to be copolymerized is not particularly limited as long as it has an adhesive functional group and can be copolymerized, but the amount and type are controlled in consideration of melt molding. It is preferable that the fluororesin of the inner layer 2 is in the melting point (° C.) range and has excellent adhesion with the fluororesin of the inner layer 1 and the barrier / adhesive resin layer (polyamide resin).
  • the adhesive functional group include an epoxy group, a hydroxyl group, a carboxylic anhydride residue, a carboxylic acid group, an acrylate group, a carbonate group, and an amino group.
  • this copolymer include the ethylene-tetrafluoroethylene-hexafluoropropylene-ethylene carbonate copolymer EFEP used in Example 1 (for example, RP5000 manufactured by Daikin Industries, Ltd.).
  • MFR (297 ° C., 5 kg load g / 10 min) (measuring method: 265 ° C., ASTM D1238) is preferably 9 to 35, more preferably 15 to 25. If it is less than 9, the melt viscosity is high and the blow melt moldability is high. There is a possibility that the drive energy will be worsened, and if it exceeds 35, the melt tension is low, and there is a risk that problems such as draw-down may occur during blow molding.
  • the specific gravity (measurement method: ASTM D-792) may be a commercially available specific gravity of 1.7 to 1.9, more preferably 1.83 to 1.89. If the specific gravity is less than 1.7, there is a concern that the adhesiveness may be lowered, and if it exceeds 1.9, the strength of the container may be insufficient.
  • the melting point (° C.) (measurement method: ASTM D792) may be a commercially available melting point of 200 to 240 ° C., more preferably 208 to 228 ° C. If the melting point is less than 200 ° C., a difference in melting point from other resins may occur, which may cause problems of adhesive strength and moldability. If the melting point exceeds 240 ° C., it may be difficult to laminate with other resins. .
  • the above-mentioned polyamide resin of the barrier and adhesive resin layer used in the present invention is an additive-free grade polyamide resin to which additives including additives and lubricants that are usually added intentionally are not added / blended.
  • additives including additives and lubricants that are usually added intentionally are not added / blended.
  • Z4887 manufactured by Daicel Evonik Co., Ltd. can be given.
  • the polyamide obtained by ring-opening polycondensation of caprolactam is at least one polyamide selected from nylon 6, nylon 11, nylon 12, nylon 66 and the like, and a polyamide that does not contain additives and additives including a lubricant is It can be preferably used.
  • the maleic anhydride-modified polyolefin resin of the adhesive layer used in the present invention has excellent adhesion to the barrier / adhesive resin layer (polyamide resin) and the barrier layer (ethylene vinyl alcohol copolymer resin). Furthermore, the maleic anhydride-modified polyolefin resin of the adhesive layer has excellent adhesion to the barrier layer (ethylene vinyl alcohol copolymer resin) and the outer layer (ultra high molecular weight high density polyethylene resin), The adhesive layer is formed by adhering the two, and any commercially available product can be used as long as it can be melt-molded.
  • the inner layers 1 and 2 fluororesin
  • Combined recovered material including barrier / adhesive resin layer (polyamide resin), adhesive layer (maleic anhydride modified polyolefin resin), barrier layer (ethylene vinyl alcohol copolymer resin) and outer layer (ultra high molecular weight high density polyethylene resin) can do. This is because the maleic anhydride-modified polyolefin resin in which the recovered material of the adhesive layer is blended is separated from the fluororesin of the inner layer 1 serving as the liquid contact surface, so that there is practically no risk of impairing cleanliness. .
  • the maleic anhydride-modified polyolefin resin having excellent adhesion to the outer layer may be the same or different, and is preferably determined by testing in advance.
  • the barrier layer ethylene vinyl alcohol copolymer resin (ethylene 24-44 mol% copolymer) used in the present invention is a resin obtained by hydrolyzing ethylene vinyl alcohol copolymer and almost completely saponified, and has an aroma retaining property. It has excellent gas barrier properties and is widely used in containers and packaging materials for chemicals, cosmetics, etc., and has high resistance to oils and organic solvents. By using a polymerized resin, oxygen barrier properties can be secured, and since MFR, melting point, etc. are close to ultrahigh molecular weight high-density polyethylene resin and excellent in stable moldability, they can be preferably used.
  • ethylene vinyl alcohol copolymer resin for the barrier layer examples include, for example, F171B (ethylene 32 mol% copolymerization, melting point 183 ° C., saponification rate 99.99%) manufactured by Kuraray Co., Ltd. be able to.
  • MFR (Characteristic) MFR (210 ° C., 2.16 kg load g / 10 min): 2 to 5 Density (Kg / m3): (ISO 1183 compliant) 1.1 to 1.3 Melting point (° C): (ISO 1346 compliant): 170-200
  • the MFR is preferably 2 to 5, more preferably 3 to 5, the density is preferably 1.1 to 1.3, more preferably 1.2 to 1.3, and the melting point (° C.). Is preferably 170 to 200, more preferably 190 to 200.
  • gas barrier properties, strength, stable moldability and the like are all excellent, but at least one of these characteristics may be impaired outside the above ranges.
  • the ultrahigh molecular weight high-density polyethylene resin of the outer layers 1 and 2 used in the present invention preferably has a density (measurement method: JIS K7112 compliant), preferably 940 to 962 Kg / m3, more preferably 944 to 946 Kg / m3.
  • the weight average molecular weight is preferably 2260 to 260,000, more preferably 240 to 260,000, and the molecular weight distribution (Mw / Mn) (measurement method: described later) is preferably 12 or less, more preferably 11 or less, melt tension (measurement method: Japanese polyethylene method, 210 ° C.
  • Ren resin is preferable, the ultra high molecular weight high density polyethylene resin such as moldability and mechanical strength by using the outer layer 1 is improved, there is no problems such as drawdown is also improved such as yield.
  • (Mw / Mn) of the ultra-high molecular weight high-density polyethylene resin forming the outer layers 1 and 2 is preferably 12 or less, more preferably 11 or less. When (Mw / Mn) exceeds 12, melt processing and rapid cooling are performed. However, the outer layer of the blow-molded laminated container that has been formed into a multilayer structure under the normal molding process conditions is not composed of a dense small crystal aggregate due to an increase or variation in the outer layer, and the mechanical strength may be insufficient.
  • the weight average molecular weight of the ultrahigh molecular weight high density polyethylene resin is less than 220,000, the mechanical strength may be insufficient, and the weight average molecular weight exceeds 260,000. Further, since the melt viscosity of the resin is high, the moldability is deteriorated, and there is a possibility that molecular cutting by shear stress may occur.
  • the density and melt tension of the ultra-high molecular weight high-density polyethylene resin forming the outer layers 1 and 2 are less than the lower limit values, it may be difficult to draw down and control the wall thickness. In addition, there is a possibility that a problem of melt fracture (rough skin) may occur.
  • ethylene homopolymers and copolymers of ethylene and ⁇ -olefins such as propylene, butene-1,4-methyl-pentene-1, hexene-1 and octene-1 are preferably used.
  • the content of ⁇ -olefin in the copolymer is preferably 15% by mass or less.
  • the molecular structure of the copolymer is atactic, isotactic, syndiotactic or a mixture thereof.
  • the low pressure method or the intermediate pressure method may be used.
  • At least one light-shielding pigment selected from organic light-shielding pigments and / or inorganic light-shielding pigments has a visible light transmittance of 1 to 500 nm. It is preferable to add a predetermined amount so that the ultraviolet transmittance at a wavelength of 200 to 400 nm is 1% or less (according to the measurement method described later).
  • the organic light-shielding pigment and the inorganic light-shielding pigment have a visible light transmittance of 1% or less at a wavelength of 500 to 800 nm and an ultraviolet transmittance of a wavelength of 200 to 400 nm when blended in a predetermined amount in the outer layer. It can be 1% or less, and is not particularly limited as long as other characteristics of the outer layer are not impaired.
  • organic light-shielding pigments such as quinacridone, phthalocyanine, anthraquinone, and monoazo
  • inorganic light-shielding properties such as carbon black, iron oxide, zinc oxide, ultramarine, chromium oxide, titanium oxide, and silicon dioxide
  • At least one light-shielding pigment selected from pigments can be used preferably in the present invention because the object can be achieved by a relatively small amount of the pigment.
  • quinacridone-based light-shielding pigment examples include TET48183 and TET78310 (manufactured by Toyocolor Co., Ltd.).
  • phthalocyanine-based light-shielding pigment examples include 7F2854 (manufactured by Dainichi Seika Kogyo Co., Ltd.), TET58335 (manufactured by Toyocolor Co., Ltd.), and EPH-525328 (manufactured by Polycol Kogyo Co., Ltd.). Can do.
  • monoazo light-shielding pigment examples include TET38013 (manufactured by Toyocolor Co., Ltd.) and ECE-6293 (manufactured by Polycol Kogyo Co., Ltd.).
  • carbon black light-shielding pigment examples include TET01337 (manufactured by Toyocolor Co., Ltd.) and EPH-K-51680 (manufactured by Polycol Kogyo Co., Ltd.).
  • iron oxide-based light-shielding pigment examples include EPH-C-1045 (manufactured by Polycol Kogyo Co., Ltd.) and TET68473 (manufactured by Toyocolor Co., Ltd.).
  • ultramarine light-shielding pigment examples include EPH-B-46662 (manufactured by Polycol Kogyo Co., Ltd.) and TET26146 (manufactured by Toyocolor Co., Ltd.).
  • titanium oxide-based light-shielding pigment examples include EB-1427 (manufactured by DIC Corporation), EPH-H-2481 (manufactured by Polycol Kogyo Co., Ltd.), and TET28318 (manufactured by Toyocolor Co., Ltd.). Can be mentioned.
  • the blending amount of the light-shielding pigment is tested in advance, and a visible wavelength of 500 to 800 nm It is preferable to determine such that the light transmittance is 1% or less and the ultraviolet transmittance at a wavelength of 200 to 400 nm is 1% or less.
  • the transmittance of visible light with a wavelength of 500 to 800 nm is 1% or less and the transmittance of ultraviolet light with a wavelength of 200 to 400 nm is 1% or less, the contents are not visible and the contained liquid content can be prevented from being altered.
  • It can be used as an ultra-high-purity chemical container such as a chemical or a fragrance that can be imparted with ultraviolet blocking properties, such as a photoresist solution, which is denatured and cured by ultraviolet rays.
  • the light-shielding pigment and the blending amount As a specific example of the light-shielding pigment and the blending amount, an example in which 2% by mass of a phthalocyanine-based light-shielding pigment (trade name: 7F2854: manufactured by Dainichi Seika Kogyo Co., Ltd.) is blended in the outer layer in Example 1 to be described later. be able to. Since 7F2854 is a master batch containing 6% by mass of phthalocyanine, in the above example, 0.012% by mass of phthalocyanine was blended in the outer layer, and the ultraviolet transmittance was 1% or less and the visible light transmittance was 1% or less. The result is obtained.
  • 7F2854 is a master batch containing 6% by mass of phthalocyanine
  • 0.012% by mass of phthalocyanine was blended in the outer layer, and the ultraviolet transmittance was 1% or less and the visible light transmittance was 1% or less. The result is obtained.
  • the outer layers 1 and 2 used in the present invention contain a predetermined amount (0.05 to 0.30% by mass) of at least one antioxidant selected from the group consisting of phenolic, phosphorus and sulfur antioxidants. It is preferable to prevent the resin from being burnt and to prevent the appearance from being deteriorated due to the burnt resin.
  • the phenolic antioxidant, phosphorus antioxidant, and sulfur antioxidant are not particularly limited as long as they have a high antioxidant action and do not impair the other characteristics of the outer layers 1 and 2.
  • phenolic antioxidants include ADEKA STAB AO60 manufactured by ADEKA Corporation.
  • phosphorus-based antioxidant include ADK STAB 2112 manufactured by ADEKA Corporation.
  • sulfur-based antioxidant include DSTP manufactured by Yoshitomi Mitsubishi Chemical Corporation.
  • antioxidants are preferably added in an amount of 0.05 to 0.30% by mass, and 0.10 to 0.25% by mass, based on the ultrahigh molecular weight high density polyethylene resin forming the outer layers 1 and 2. More preferably. If it is less than 0.05% by mass, the antioxidant performance may be inferior, and if it exceeds 0.30% by mass, the additive may bleed out on the surface of the container.
  • the outer layers 1 and 2 used in the present invention are blended with light-shielding pigments and antioxidants that can become impure fine particles, but the outer layers 1 and 2 are separated from the inner layers 1 and 2 that are in contact with the liquid. Since the barrier / adhesive resin layer 2, the adhesive layers 3, 5, and the barrier layer 4 prevent the impure fine particles due to the light-shielding pigment, antioxidant, etc. from leaching into the content liquid, they are stored in a container. Do not leach into chemicals.
  • a light-resistant stabilizer such as a benzotriazole-based light-resistant stabilizer and a triazine-based light-resistant stabilizer can be appropriately used for the outer layers 1 and 2 as necessary, together with the light-shielding pigment.
  • a benzotriazole light stabilizer or a triazine light stabilizer can block UV-B (200 to 320 nm) and UV-A (320 to 400 nm), respectively.
  • the ultraviolet blocking property can be remarkably improved without deteriorating.
  • Examples of the light-resistant stabilizer include 2- (5-methyl-2-hydroxyphenyl) benzotriazole, 2- (3-tert-butyl-5-methyl-2-hydroxyphenyl) -5-chlorobenzotriazole, 2- (2 -Hydroxy-5-methylphenylbenzotriazole), 2- (5-chloro-2-benzotriazole) -6-t-butyl-cresol, 2- (3,5-di-t-amino-2-hydroxyphenyl) Benzotriazole light stabilizers such as bendtriazole and 2- (2H-benzotriazol-2-yl) -p-cresol, 2- [4,6-di (2,4xylyl) -1,3,5-triazine -2-yl] -5,2,4,6-tris (2-hydroxy-4-hexyloxy-3-methylphenyl) -1,3,5-triazine, 2- (4,6-diphe 1,3,5-triazin-2-yl) -5- [2-
  • the content of the additive contained in the resin is a value obtained by separating and quantifying the extracted solution extracted with a Soxhlet extractor using tetrahydrofuran (THF) for 8 hours by liquid chromatography.
  • the measurement conditions are as follows: GULIVER (manufactured by JASCO Corporation), column is Finepak® GEL-101 (manufactured by JASCO Corporation), solvent is THF, detector is UV-970 (manufactured by JASCO Corporation) and 830-RI. (Manufactured by JASCO Corporation).
  • the resin composition cut out from the container is dissolved in a solvent (orthodichlorobenzene) to form a sample solution, and the molecular weight and molecular weight distribution are measured by GPC.
  • the weight average molecular weight and the number average molecular weight are calculated by the following equations.
  • Weight average molecular weight Mw ⁇ (M ⁇ w) / ⁇ w (2)
  • Number average molecular weight Mn ⁇ w / ⁇ (w / M) (3)
  • Molecular weight distribution weight average molecular weight / number average molecular weight (Mw / Mn)
  • M is molecular weight and w is a weight fraction.
  • GPC measurement conditions were 150 CV (manufactured by Waters) for the apparatus, TSKgel GMH-HT (manufactured by Tosoh Corporation) for the column, orthodichlorobenzene for the solvent, temperature of 138 ° C., and a detector for the differential refractometer. .
  • the raw material resin In order to control the molecular weight distribution of the container within the above range, the raw material resin must also have a certain range of molecular weight distribution.
  • the molding method is not particularly limited as long as it can form the chemical-resistant blow molded laminate container excellent in transparency of the present invention by the blow molding method. It can also be used by selecting from a molding machine.
  • Example 1 The inner layer 1 is MFR 25 g / 10 min, the specific gravity is 1.86, the melting point is 223 ° C., and the additive-free fluororesin (EP-610 manufactured by Daikin Industries, Ltd.) having a loss on heating of 0.16% by mass is used.
  • the inner layer 2 is MFR 25 g.
  • additive-free fluororesin (RP-5000 manufactured by Daikin Industries, Ltd.) having a loss on heating of 0.35% by mass is used as a barrier and adhesive resin layer
  • Additive-free polyamide resin (Z4887, manufactured by Daicel Evonik Co., Ltd.) having a function of adhering to the fluororesin of the inner layer 2 and containing no additive that is intentionally added or a lubricant. 87), and maleic anhydride-modified polyolefin resin (Nippon Polyethylene Co., Ltd.) as an adhesive layer having an adhesive function between the polyamide resin and the barrier layer.
  • T71A and a barrier resin (ethylene-vinyl alcohol copolymer resin F171B: manufactured by Kuraray Co., Ltd., saponification rate 99.99%) as the barrier layer, and ultrahigh molecular weight high-density polyethylene as the outer layer 1
  • Maleic anhydride-modified polyolefin resin for resin (HB111R manufactured by Nippon Polyethylene Co., Ltd.) (HL-MFR (measurement method: JIS K7112) 6 g / 10 min, density 946 Kg / m3, weight average molecular weight 250,000, melt tension 25 g) (Nippon Polyethylene Co., Ltd.
  • FT71A 30% by mass
  • phthalocyanine-based light-shielding pigment (trade name: 7F2854: manufactured by Dainichi Seika Kogyo Co., Ltd., containing 6% by mass of phthalocyanine) Masterbatch) 2% by mass
  • phenolic antioxidant as antioxidant (trade name: ADK STAB O60: ADEKA Co., Ltd.)
  • phosphorus antioxidant (trade name: ADK STAB 2112: ADEKA Co., Ltd.) in a total of 0.2% by mass were used, and the following high molecular weight high density polyethylene resin was used.
  • the chemical-resistant blow molded laminated container of the present invention consisting of 6 layers (total mass 400 g, inner layer 1 50 ⁇ m, inner layer 2 100 ⁇ m, barrier and adhesive resin layer 50 ⁇ m, adhesiveness) Layer 50 ⁇ m, barrier layer 50 ⁇ m, outer layer 1 1500 ⁇ m, average total wall thickness 1.8 mm, capacity 3750 ML).
  • IR Affinity-1 manufactured by Shimadzu Corporation
  • Measurement sample A 50 ⁇ m-thick film sheet of inner layers 1 and 2 was prepared using a 240 ° C. press.
  • Measurement wavelength 600 to 4000 cm-1
  • FIG. 3 shows the result of infrared spectroscopic analysis of the inner layer 1, wherein the vertical axis represents absorbance (%) and the horizontal axis represents wavelength (cm-1).
  • FIG. 4 shows the result of infrared spectroscopic analysis of the inner layer 2, wherein the vertical axis represents absorbance (%) and the horizontal axis represents wavelength (cm-1).
  • a large sharp absorption (indicated by an arrow) at a wavelength of 1800 (cm-1) in FIG. 4 is an absorption peak of a carbonate group, and it can be seen that the fluororesin of the inner layer 2 has an adhesive functional group (carbonate group).
  • the fluororesin of the inner layer 2 is produced by copolymerizing the monomer ( ⁇ ) having an adhesive functional group as described above, and the fluororesin of the inner layer 2 depends on the copolymerization amount of the monomer ( ⁇ ).
  • the amount of the adhesive functional group can be controlled, thereby controlling the adhesiveness of the fluororesin of the inner layer 2 so that the inner layer 2 has good adhesion to the fluororesin of the inner layer 1 and the barrier / adhesive resin layer.
  • the melting point and the like can be controlled to be within the predetermined range.
  • the large sharp absorption peak is not observed at a wavelength of 1800 (cm-1) in FIG. 3, indicating that the fluororesin of the inner layer 1 does not have an adhesive functional group (carbonate group).
  • the inner layer 1 has good adhesion to the fluororesin of the inner layer 2 but does not have adhesion to other layers.
  • the large and sharp absorption peak of wavelength 3000 (cm-1) in FIGS. 3 and 4 is an absorption peak derived from copolymerized ethylene.
  • Test method Measurement method of impure particles
  • the following measurements are performed in a clean room (Class 100).
  • Measuring apparatus A particle counter “KL-26” RION KL-26 manufactured by Rion Co., Ltd. is used.
  • Sample to be measured filled with ultrapure water in a molded container and stored at 23 ° C. immediately after extraction and for 30 days and extracted or stored at 40 ° C. immediately after extraction and for 30 days and extracted, then 20 in an upright state A sample obtained by collecting a measurement sample from a container that has been allowed to stand for minutes is taken as a measurement sample.
  • the particle counter Prior to measurement, the particle counter is purged with ultrapure water, and then the measuring device is washed twice with 25 ml of ultrapure water.
  • Oxygen permeability [cm3 / (pg.24h.atm)]: Using a 3.75L container (wall thickness at the center of the bottle: 1.8 mm), using the measuring device (OX-TRAN2 / 21) (manufactured by MOCON) in accordance with JIS K7126-2, from the outside of the container The oxygen transmission to the inside was measured. Temperature and humidity: 1 atm outside, 23 ° C., 50% RH oxygen. Inside 1 atm, 23 ° C., dry nitrogen.
  • UV transmittance Using JASCO Corporation V-670, the transmittance in the ultraviolet region of 200 to 400 nm is obtained.
  • fragrances include limonene (trade name: orange oil, purity 96.4%, manufactured by Hasegawa Fragrance Co., Ltd.), citrus fruits (trade name: lemon essence, manufactured by Hasegawa Fragrance Co., Ltd.), crab oil (15%) Dimethyl sulfide, propylene glycol solution, manufactured by Hasegawa Fragrance Co., Ltd.), rice salad (trade name: rice oil, manufactured by Hasegawa Fragrance Co., Ltd.), ethyl butyrate (trade name: esters, purity 100%, Hasegawa Fragrance Co., Ltd.) ), Trans-2-hexenal (trade name: aldehydes, purity 99.7%, manufactured by Hasegawa Fragrance Co., Ltd.), filled with 1 kg of each fragrance, sealed, sealed at room temperature and pressure for 1 month and Left for 3 months.
  • crab oil (15% dimethyl sulfide, propylene glycol solution) was refrigerated at room temperature and pressure for 1 month and 3 months. After standing for 3 months, measure the container mass for each sample and check if the contents are dissipated, conduct a sensory test with 10 panel members to check whether it has been altered, and determine the specific gravity and refractive index. It was measured to check whether it was fluctuating, and for a sample that could be analyzed, the components were checked by a gas chromatograph and evaluated according to the following evaluation criteria.
  • Evaluation criteria There is no dissipation, alteration, fluctuation, etc., storage stability is high, and there is marketability.
  • ⁇ Slightly inferior to ⁇ , but practically free from dissipation, alteration, fluctuation, etc., and has high storage stability and marketability.
  • X There are dissipation, alteration, fluctuation, etc., storage stability is low, and there is no marketability.
  • the particle value after 23 days at 30 ° C. is 5 particles / ml or less, and the particle value after 30 days at 40 ° C. is 10 particles / ml or less, Oxygen permeability is 0.003 [cm3 / (pg.24 h.atm)] or less, UV transmittance is 1% or less, Visible light transmittance is 1% or less, Visibility is ⁇ (the internal tap water cannot be confirmed), Drop strength: no destruction, Perfume is appropriate ⁇ ⁇ ⁇ , Metal elution is 10 (ng / L) or less. If all pass, pass the overall judgment. If any of these is inferior to the above, the overall judgment is judged as x.
  • Example 1 Comparative Example 1
  • an antioxidant hindered phenol-based antioxidant, A blow-molded laminated container for comparison was made and evaluated in the same manner as in Example 1 except that the same polyamide resin containing 2000 ppm) (relative viscosity 1.87) was used. The results are shown in Tables 1 and 2.
  • a blow molded laminated container for comparison was made and evaluated in the same manner as in Example 1 except that a wetted layer using 0.2% by mass of high density polyethylene (9D01A manufactured by Tosoh Corporation) was used. . The results are shown in Tables 1 and 2.
  • Example 3 (Comparative Example 3) In the same manner as in Example 1, except that the inner layer 1 used in Example 1 was not used and the inner layer 2 having a heat loss of 0.35% by mass used in Example 1 was used as the wetted layer, A blow molded laminated container was made and evaluated. The results are shown in Tables 1 and 2.
  • Comparative Example 4 The fluororesin of the wetted layer used in Comparative Example 3 was heated at an electric furnace temperature of 260 ° C. ⁇ 1 ° C. for 120 minutes to reduce the loss on heating (heating loss of 0.31% by mass). In the same manner as in Comparative Example 3, a blow molded laminated container for comparison was made and evaluated. The results are shown in Tables 1 and 2.
  • the chemical-resistant blow-molded laminated container of Example 1 has a particle value, oxygen transmittance, ultraviolet transmittance, visible light transmittance, visibility, drop strength, perfume suitability, metal elution It can be seen that the container for comparison of Comparative Examples 1 to 6 is inferior in any one of the above, while the overall judgment is excellent.
  • the chemical-resistant blow-molded laminated container of the present invention does not have an adhesive functional group as the inner layer 1 and has adhesiveness to the fluororesin of the inner layer 2 but not to other layers.
  • the inner layer 2 has an adhesive functional group, and has adhesiveness to the fluororesin of the inner layer 1 and the barrier / adhesive resin layer.
  • the said polyamide which does not contain the additive which contains the additive and lubricant which are intentionally added to a barrier and adhesive resin layer using the specific fluororesin whose loss on heating is 0.40 mass% or less which has an additive free
  • the cleanliness is 5 or less after storage at 23 ° C.
  • the oxygen barrier properties are improved, and the outer layer has a high UV-blocking property with a high melt tension.
  • Use of ultra-high molecular weight, high-density polyethylene resin that excels in visible light resistance and mechanical strength improves moldability and UV blocking properties, so expensive and highly dangerous chemicals such as fragrances and photoresist solutions
  • As a container for ultra-high-purity chemicals there is no visibility of the contents, and there is a remarkable effect of providing a chemical-resistant blow-molded laminated container with a small amount of impure particulate elution. Is expensive.

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Ceramic Engineering (AREA)
  • Containers Having Bodies Formed In One Piece (AREA)
  • Laminated Bodies (AREA)

Abstract

L'invention concerne un récipient stratifié moulé par soufflage résistant aux produits chimiques dans lequel sont stratifiées dans l'ordre depuis son côté interne vers son côté externe : une couche interne (1) (résine fluorée exempte de groupe fonctionnel adhésif, sans agent d'addition et de perte à la chaleur inférieure ou égale à 0,20% en masse) ; une couche interne (2) (résine fluorée possédant un groupe fonctionnel adhésif, sans agent d'addition et de perte à la chaleur inférieure ou égale à 0,40% en masse) ; une couche de résine à la fois barrière et adhésive (polyamide sans additif) ; une couche adhésive (résine de polyoléfine modifiée par un anhydride maléique) ; une couche barrière (résine copolymère d'éthylène et alcool vinylique) ; et une couche externe (1) (résine de polyéthylène de masse moléculaire très élevée et de haute densité contenant un pigment bloquant la lumière et une résine de polyoléfine modifiée par un anhydride maléique. L'objet de l'invention présente une transmittance de la lumière visible inférieure ou égale à 1%, un facteur de transmission des ultraviolets inférieur ou égal à 1%, et une quantité d'élution de microparticules impures (nombre/ml) après stockages à 23°C et 40°C, respectivement inférieure ou égale à 5 et inférieure ou égale à 10. Enfin, l'objet de l'invention est doté d'excellentes propriétés d'écran aux ultraviolets et de barrière à l'oxygène, possède une faible élution des particules impures, et ne présente pas de visibilité de son contenu.
PCT/JP2016/002928 2016-06-17 2016-06-17 Récipient stratifié moulé par soufflage résistant aux produits chimiques de faible quantité d'élution de microparticules impures WO2017216827A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2018522901A JP6518840B2 (ja) 2016-06-17 2016-06-17 不純微粒子溶出量の少ない耐薬品性吹込み成形積層容器
CN201680086864.7A CN109311553B (zh) 2016-06-17 2016-06-17 杂质微粒溶出量少的耐化学药品性吹塑成型层叠容器
KR1020197001662A KR102192237B1 (ko) 2016-06-17 2016-06-17 불순 미립자 용출량이 적은 내약품성 취입 성형 적층 용기
PCT/JP2016/002928 WO2017216827A1 (fr) 2016-06-17 2016-06-17 Récipient stratifié moulé par soufflage résistant aux produits chimiques de faible quantité d'élution de microparticules impures

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2016/002928 WO2017216827A1 (fr) 2016-06-17 2016-06-17 Récipient stratifié moulé par soufflage résistant aux produits chimiques de faible quantité d'élution de microparticules impures

Publications (1)

Publication Number Publication Date
WO2017216827A1 true WO2017216827A1 (fr) 2017-12-21

Family

ID=60663029

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2016/002928 WO2017216827A1 (fr) 2016-06-17 2016-06-17 Récipient stratifié moulé par soufflage résistant aux produits chimiques de faible quantité d'élution de microparticules impures

Country Status (4)

Country Link
JP (1) JP6518840B2 (fr)
KR (1) KR102192237B1 (fr)
CN (1) CN109311553B (fr)
WO (1) WO2017216827A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019245889A1 (fr) * 2018-06-18 2019-12-26 Baker Hughes, A Ge Company, Llc Procédés de fabrication d'agents de réduction de traînée de polyoléfine
US11199296B2 (en) 2019-06-14 2021-12-14 Baker Hughes Oilfield Operations Llc Drag reducing agents

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3722086A1 (fr) * 2019-04-12 2020-10-14 Nitto Denko Corporation Films multicouches pour des applications d'airbag

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001058686A1 (fr) * 2000-02-10 2001-08-16 Daikin Industries, Ltd. Resine stratifiee
JP2010042824A (ja) * 2008-08-11 2010-02-25 Aicello Chemical Co Ltd 収容薬品視認性紫外線遮断多層容器
JP2013508235A (ja) * 2009-11-05 2013-03-07 ザ プロクター アンド ギャンブル カンパニー 感光性液体組成物を保護するための包装製品
WO2013125515A1 (fr) * 2012-02-22 2013-08-29 キョーラク株式会社 Récipient de protection contre la lumière
JP2015123351A (ja) * 2013-12-27 2015-07-06 コダマ樹脂工業株式会社 耐薬品性吹込み成形積層容器
JP2015123744A (ja) * 2013-12-27 2015-07-06 コダマ樹脂工業株式会社 透明性に優れた耐薬品性吹込み成形積層容器

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2749513B2 (ja) 1994-03-24 1998-05-13 アイセロ化学株式会社 高純度溶剤用容器
JP2805723B2 (ja) * 1994-06-09 1998-09-30 アイセロ化学株式会社 高純度薬品用遮光容器
JP2805188B2 (ja) 1994-10-19 1998-09-30 アイセロ化学株式会社 高純度薬品用容器
FR2765520B1 (fr) * 1997-07-03 1999-08-27 Nyltech Italia Structure multicouche a base de polyamides et tube ou conduit a structure multicouche
JP4167745B2 (ja) 1998-04-08 2008-10-22 アイセロ化学株式会社 高純度薬品液用容器および高純度薬品液の排出方法
WO2005102694A1 (fr) * 2004-04-27 2005-11-03 Ube Industries, Ltd. Structure multicouche
CN201350980Y (zh) * 2008-12-15 2009-11-25 郭锡南 复合瓶

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001058686A1 (fr) * 2000-02-10 2001-08-16 Daikin Industries, Ltd. Resine stratifiee
JP2010042824A (ja) * 2008-08-11 2010-02-25 Aicello Chemical Co Ltd 収容薬品視認性紫外線遮断多層容器
JP2013508235A (ja) * 2009-11-05 2013-03-07 ザ プロクター アンド ギャンブル カンパニー 感光性液体組成物を保護するための包装製品
WO2013125515A1 (fr) * 2012-02-22 2013-08-29 キョーラク株式会社 Récipient de protection contre la lumière
JP2015123351A (ja) * 2013-12-27 2015-07-06 コダマ樹脂工業株式会社 耐薬品性吹込み成形積層容器
JP2015123744A (ja) * 2013-12-27 2015-07-06 コダマ樹脂工業株式会社 透明性に優れた耐薬品性吹込み成形積層容器

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019245889A1 (fr) * 2018-06-18 2019-12-26 Baker Hughes, A Ge Company, Llc Procédés de fabrication d'agents de réduction de traînée de polyoléfine
US10982017B2 (en) 2018-06-18 2021-04-20 Baker Hughes, A Ge Company, Llc Methods of manufacturing polyolefin drag reducing agents
US11199296B2 (en) 2019-06-14 2021-12-14 Baker Hughes Oilfield Operations Llc Drag reducing agents
US11248748B2 (en) 2019-06-14 2022-02-15 Baker Hughes Oilfield Operations Llc Drag reducing agents

Also Published As

Publication number Publication date
KR20190020078A (ko) 2019-02-27
CN109311553B (zh) 2020-04-07
JPWO2017216827A1 (ja) 2019-02-21
JP6518840B2 (ja) 2019-05-22
CN109311553A (zh) 2019-02-05
KR102192237B1 (ko) 2020-12-17

Similar Documents

Publication Publication Date Title
JP5898172B2 (ja) 耐薬品性吹込み成形積層容器
JP6073980B2 (ja) 内容物の視認性に優れた超高純度薬品用吹込み成形積層容器
WO2017216827A1 (fr) Récipient stratifié moulé par soufflage résistant aux produits chimiques de faible quantité d'élution de microparticules impures
JP5706512B1 (ja) 透明性に優れた耐薬品性吹込み成形積層容器
JP5753746B2 (ja) ポリエチレン系多層フィルム
CN101360605A (zh) 耐候性多层膜
WO2015053334A1 (fr) Composition de résine de polyéthylène, stratifié la comprenant et contenant médical utilisant le stratifié
JP6005580B2 (ja) ポリエチレン系多層フィルム
US20130026127A1 (en) PVC-Free Seals for Twist Crowns
US20150290077A1 (en) Medical container
WO2017216826A1 (fr) Récipient stratifié moulé par soufflage résistant aux produits chimiques de transparence excellente et de faible quantité d'élution de microparticules impures
EP2683772B1 (fr) Composition antibuée scellable pour films thermoscellables et emballages à ouverture facile obtenus à partir de celle-ci
JP6839489B2 (ja) 内容物の視認性がない超高純度薬品用吹込み成形積層容器
KR102092982B1 (ko) 투명성이 우수한 내약품성 취입 성형 적층 용기
TWI613124B (zh) 透明性優良耐化學藥品性吹塑積層容器
WO2005110743A1 (fr) Film d'emballage haute barrière ayant des matières extractibles reduites
CA2342050A1 (fr) Film transparent, a moulage profond et a scellage rapide possedant des proprietes de filtration du rayonnement ultraviolet
WO2022118680A1 (fr) Film de résine à base de polypropylène à orientation biaxiale, et emballage mettant en œuvre celui-ci
KR102590937B1 (ko) 열접착성과 내충격성이 우수한 폴리프로필렌 블록 공중합체 수지
EP3212396A1 (fr) Récipients multicouches moulés par soufflage ayant une retenue de produit réduite
EP4166317A1 (fr) Récipient tubulaire flexible pour pcr
JP6855725B2 (ja) 直線易カット性フィルムの製造方法及び直線易カット性フィルム
KR200240406Y1 (ko) 고순도 약품보존용 차광성 플라스틱 용기
KR20160082565A (ko) 방담필름 및 제조방법
KR20020082242A (ko) 고순도 약품보존용 차광성 플라스틱 용기

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref document number: 2018522901

Country of ref document: JP

Kind code of ref document: A

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 16905382

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20197001662

Country of ref document: KR

Kind code of ref document: A

122 Ep: pct application non-entry in european phase

Ref document number: 16905382

Country of ref document: EP

Kind code of ref document: A1