EP0873946B1 - Aerosol container - Google Patents
Aerosol container Download PDFInfo
- Publication number
- EP0873946B1 EP0873946B1 EP19980107302 EP98107302A EP0873946B1 EP 0873946 B1 EP0873946 B1 EP 0873946B1 EP 19980107302 EP19980107302 EP 19980107302 EP 98107302 A EP98107302 A EP 98107302A EP 0873946 B1 EP0873946 B1 EP 0873946B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- aerosol container
- agents
- container
- aerosol
- temperature
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 239000000443 aerosol Substances 0.000 title claims description 43
- 229920001230 polyarylate Polymers 0.000 claims description 15
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 13
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 13
- -1 poly(ethylene naphthalate) Polymers 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 239000002994 raw material Substances 0.000 claims description 8
- 230000009477 glass transition Effects 0.000 claims description 7
- 238000000071 blow moulding Methods 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000004695 Polyether sulfone Substances 0.000 claims description 2
- 229920002492 poly(sulfone) Polymers 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920006393 polyether sulfone Polymers 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 description 29
- 230000000052 comparative effect Effects 0.000 description 8
- 239000002917 insecticide Substances 0.000 description 8
- 239000003915 liquefied petroleum gas Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000002304 perfume Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000003380 propellant Substances 0.000 description 3
- 239000012808 vapor phase Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000011928 denatured alcohol Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 206010012504 Dermatophytosis Diseases 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241001460074 Microsporum distortum Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 208000002474 Tinea Diseases 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000013040 bath agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000000551 dentifrice Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000010413 gardening Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008266 hair spray Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 210000000214 mouth Anatomy 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- 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
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/14—Containers for dispensing liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant
- B65D83/38—Details of the container body
Definitions
- the present invention relates to an aerosol container in which a valve cap is fitted into an opening at the neck and particularly, to a raw material which is used for producing the aerosol container.
- an aerosol container in which a valve cap is fitted into an opening at the neck the one having such a structure as shown in a cross-sectional view of Figure 2 is disclosed in, for example, Japanese Patent KOKAI (Laid-Open) No.76993/88.
- This structure is the one in which ring recess (3) is formed on the neck of the container body (1); and valve cap (7) is fitted into the above-mentioned neck region (2) and the lower end (8) of the valve cap (7) is narrowed down into the above-mentioned recess (3), wherein valve housing (5) for valve (4) extending into the inside of the container, is airtightly supported with sealing member (6).
- a high pressure-resistant property is requested for the container in itself, so that a resin such as polyethylene terephthalate is commonly used in the form of a single substance for a raw material of the container.
- an aerosol container in which a valve cap is fitted into an opening at the neck of the aerosol container, characterized in that the raw material forming the aerosol container is a high molecular compound having a glass-transition temperature of 74°C -100°C.
- the aerosol container of the present invention when the internal pressure thereof has come up to such a degree as the contents would be exploded, the aerosol container is expanded in itself to lower the internal pressure, so that a burst of the container can be avoided.
- the glass-transition temperature of a raw material for the aerosol container is set in the range of 74 °C to 100°C, preferably 75°C to 85°C.
- this glasstransition temperature is less than 74°C, the container is easily expanded in itself, while when the temperature is more than 100°C, the container is not expanded since the container is hard in itself.
- the bottom region thereof is little drawn, so that the bottom region is provided with a lower strength as compared with other regions, and thus, it causes the result that the bottom region having a lower pressure-resistant property is exploded.
- a high molecular compound having the above-mentioned glass-transition temperature can be properly selected and employed.
- polycarbonate, poly(ethylene naphthalate), polysulfone, polyethersulfone, a mixture of polyethyleneterephthalate (PET) and polyarylate (PAr) and the like can be exemplified.
- PET polyethyleneterephthalate
- PAr polyarylate
- it is the mixture of PET and PAr, wherein a mixture ratio of PET to PAr by weight % is preferably 60:40 to 95:5, more preferably 80: 20 to 95:5 by weight %.
- a biaxial stretching blow-molding hot-parison method comprises feeding a parison obtained through an injection molding while its hot state, to a rcheating process without staying, followed by forming and thereafter, mechanically drawing the parison in a longitudinal direction while the parison is maintained at a constant temperature in a blow-die; and at the same time or in succession, blowing a pressed air into the blow-die so as to expand the parison in a circular direction (or in a transverse direction).
- an aerosol container which comprises forming the engaged region of the valve cap on the periphery of the opening according to a non-stretching injection molding; and forming a body of the container which is filled with contents, according to a stretch blow-molding.
- a stretch blow-molding the longitudinal drawing of the body and the transverse drawing thereof are controlled to a low stretch ratio of 1.00 to 1.15 times and 1.90 to 2.20 times, respectively, and thereby, the container can be deformed and expanded under a high pressure following a temperature elevation of the contents and thus, the thickness thereof can be thinned so as to lower the internal pressure.
- an aerosol container of the present invention can be filled with, conventionally known ones can be employed.
- contents for example, human-body articles, domestic articles, industrial articles can be exemplified.
- human-body articles there are hair articles, cosmetics, odor-removing/sweat-repressing agents and other human-body articles;
- domestic articles there are insecticides, coating agents, cleaners, foods and other domestic articles;
- industrial articles there are automobile articles and other industrial articles.
- hairsetting sprays As for the above-mentioned hair articles, there are hairsetting sprays, hairdressing conditioners, hair shampoos, rinses, acid wool-dyeing agents, oxidizing two-agent type permanent wool-dyeing agents, color sprays, decoloring agents, permanent-wave agents, hair-growing agents and the like.
- cosmetics there are shaving creams, aftershave lotions, perfumes, eau de Cologne, face-cleansing agents, anti-suntan agents, foundations, dehairing/decoloring agents, bath agents, dentifrice agents and the like.
- odor-removing/sweat-repressing agents there are odor-removing agents, sweat-repressing agents, body shampoos and the like.
- muscle-antiflash agents As other human-body articles, there are muscle-antiflash agents, skin-trouble agents, medicines for a dermatophytosis, other medicines, injurious-insect repellents, cooling agents, cleaning-wiping agents, agents for oral-cavity and the like.
- insecticides there are space insecticides, insecticides for a cockroach, gardening insecticides, insecticides for a tick, insecticides for an uncomfortable insect and the like.
- coating agents there are domestic paints, automobile paints, undercoating agents and the like.
- cleaners there are domestic cleaners for glass, lens cleaners, carpet cleaners, bath cleaners, lustering cleaners for a floor/furniture, shoe/leather cleaners, wax lustering agents and the like.
- domestic cleaners there are indoor odor-removing agents, toilet odor-removing agents, waterproofing agents, washing starches, herbicides, clothing insecticides, flameproofing agents and the like.
- defogging agents there are defogging agents, thawing agents, engine-starting agents, puncture-repairing agents, engine cleaners and the like.
- lubricating/anti corrosive agents adhesive agents, metal deep-cut agents, mold releasing agents and the like.
- a liquid, a fluid state, a semi-solid state, a foam state, a gaseous state, as well as a mixture of each of the above-mentioned states and a little solid in a powder state or a particle state, and the like can be properly selected and employed.
- the above-mentioned contents can include a material which has been conventionally employed as an additive agent.
- an additive agent a material which has been conventionally employed as an additive agent.
- an additive agent alcohol; a synthetic resin; a propellant (a simple substance selected from the group consisting of LPG (liquefied petroleum gas), DME (dimethyl ether), N 2 CO 2 and the like, or a mixture thereof); cellulose; ammonium; water; perfumes; dyes; surface active agents; pigments are properly selected and added thereto.
- some of the above-mentioned hair sprays include a denatured alcohol and LPG for the propellant as main components, to which an acrylic resin alkanolamine liquid, polyoxyethyleneoleyl ether, a perfume and the like are added, while some of the above-mentioned hair treatments include the denatured alcohol and LPG for the propellant as main components, to which a liquid paraffin, propylene glycol, methylphenyl polysiloxane and a perfume are added.
- An aerosol container shown in Figure 1 has a content volume of 97ml and a weight of 30g, wherein reference numeral (10) is an opening of the aerosol container, which is an engagement region for engaging a valve cap (which is not shown in Figure 1), and reference numeral (11) is a body for retaining contents therein.
- the aerosol containers were formed according to a biaxial stretching blow-molding hot-parison method, after mixing PET and PAr in mixing ratios as shown in Table 1.
- a preheating temperature of 140 °C to 165°C and a heating time of 20 seconds were employed at a heating position, while a blow-die temperature of 20°C, a blow-pressure of 20 to 35kgf/cm 2 and a blow-time of 10 to 15 seconds were employed at a stretching position.
- the stretch ratio of the body of each of bottles were 1.1 times in the longitudinal direction and 2.0 times in the transverse direction.
- each of the aerosol containers was filled with contents and an aqueous solution containing LPG (liquefied petroleum gas) under the conditions of an ordinary temperature (about 25°C ) and an internal pressure of 6kg/cm 2 and then, a valve cap as shown in Figure 2 was fitted into the opening.
- LPG liquefied petroleum gas
- an environmental temperature was elevated from an ordinary temperature (about 25 °C )
- the temperature of 80°C was maintained for a period of eight hours, and then it was visually evaluated whether an engagement region which is positioned on the periphery of the opening of each of the aerosol containers had been broken or not.
- composition of contents used here are as follows: ⁇ Hair Spray> Weight% Acrylic Resin Alkanolamine Liquid (3%) 4.00 Polyoxyethyleneoleyl Ether 0.01 Triethanolamine 0.50 Perfume 0.17 Denatured Ethyl Alcohol of 99% 55.32 LPG 40.00 100.00 PET wt.% PAr wt.% Glass Transition Temperature Evaluation at Temperature Elevated to 80°C Comparative Examples 1 100 0 73 Engagement Region was Broken at 75°C in Middle of Elevation Working Examples 1 95 5 75 Not Broken 2 88 12 78 Not Broken 3 80 20 81 Not Broken 4 68 32 88 Not Broken 5 60 40 95 Not Broken Comparative Examples 2 50 50 102 Occurrence of Burst at Container Bottom
- Aerosol containers which were produced in the same mixing ratios as the ones in the Comparative Example 1 and Working Example 1 were filled with the same contents under an internal pressure of 6 kg/cm 2 , respectively, and the environmental temperature was elevated. At this time, the temperature of vapor phase in the aerosol containers, the temperature of liquid-phase in the aerosol containers, the internal pressure in the aerosol containers, and the visual evaluation as to whether the engagement regions were broken are shown in Table 2.
- the engagement region was not broken by using a aerosol container-forming raw material composed of a mixture of polyarylate with polyethylene terephthalate, even if a vapor-phase temperature is 71°C, and an internal pressure is in the range of 12 to 13kg/cm 2 . This is, because the container was expanded in itself, and its thickness was thinned, and thereby, the internal pressure was decreased.
- an aerosol container in which a valve cap is fitted into an opening of the container is produced to have a glass transition temperature of a raw material of the aerosol container in the range of 74 °C to 100°C, and thereby, such an effect that the aerosol container in itself maintains a high pressure resistance, while even if the internal pressure of the aerosol container is increased, the valve cap or the contents there of are not explosively scattered out of the container can be provided.
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Containers And Packaging Bodies Having A Special Means To Remove Contents (AREA)
- Nozzles (AREA)
- Cosmetics (AREA)
Description
- The present invention relates to an aerosol container in which a valve cap is fitted into an opening at the neck and particularly, to a raw material which is used for producing the aerosol container.
- Conventionally, an aerosol container in which a valve cap is fitted into an opening at the neck, the one having such a structure as shown in a cross-sectional view of Figure 2 is disclosed in, for example, Japanese Patent KOKAI (Laid-Open) No.76993/88. This structure is the one in which ring recess (3) is formed on the neck of the container body (1); and valve cap (7) is fitted into the above-mentioned neck region (2) and the lower end (8) of the valve cap (7) is narrowed down into the above-mentioned recess (3), wherein valve housing (5) for valve (4) extending into the inside of the container, is airtightly supported with sealing member (6). Regarding such an aerosol container, a high pressure-resistant property is requested for the container in itself, so that a resin such as polyethylene terephthalate is commonly used in the form of a single substance for a raw material of the container.
- However, since such an aerosol container is produced taking into consideration only the pressure-resistant property of the container in itself, the pressure-resistant effect of the container in itself is elevated rather than the engagement force of the valve cap. There has been the disadvantage that when the aerosol container was left as it is, for example, in a car as parked under the blazing sun, the container in itself is not bursted, but the engagement region is broken, so that the contents are jetted out from the container body while the valve cap is explosively scattered out.
- It is an object of the present invention to provide an aerosol container, out of which a valve cap and contents therein are not explosively scattered even if an internal pressure of the aerosol container is elevated, while a high pressure-resistant property of the container in itself is maintained.
- According to the present invention, there is provided an aerosol container in which a valve cap is fitted into an opening at the neck of the aerosol container, characterized in that the raw material forming the aerosol container is a high molecular compound having a glass-transition temperature of 74°C -100°C.
- In the aerosol container of the present invention, when the internal pressure thereof has come up to such a degree as the contents would be exploded, the aerosol container is expanded in itself to lower the internal pressure, so that a burst of the container can be avoided. In order to provide such a function, the glass-transition temperature of a raw material for the aerosol container is set in the range of 74 °C to 100°C, preferably 75°C to 85°C. When this glasstransition temperature is less than 74°C, the container is easily expanded in itself, while when the temperature is more than 100°C, the container is not expanded since the container is hard in itself. In this respect, when the container is produced, the bottom region thereof is little drawn, so that the bottom region is provided with a lower strength as compared with other regions, and thus, it causes the result that the bottom region having a lower pressure-resistant property is exploded.
-
- Figure 1 is a schematic elevation view of an aerosol container which is used for working examples and comparative examples of the present invention; and
- Figure 2 is a longitudinal section view in which elements in and around the opening of a conventional aerosol container are shown on an enlarged scale.
-
- As a raw material forming the aerosol container of the present invention, a high molecular compound having the above-mentioned glass-transition temperature can be properly selected and employed. For example, polycarbonate, poly(ethylene naphthalate), polysulfone, polyethersulfone, a mixture of polyethyleneterephthalate (PET) and polyarylate (PAr) and the like can be exemplified. Preferably, it is the mixture of PET and PAr, wherein a mixture ratio of PET to PAr by weight % is preferably 60:40 to 95:5, more preferably 80: 20 to 95:5 by weight %. If the compounded content of PAr is too little, the ability to engage between the aerosol container and the valve cap thereof is decreased, while if the compounded content of PAr is too much, the container comes to be difficult to expand in itself, so that the bottom region having a low pressure-resistant property is bursted out.
- Then, as a method of forming the aerosol container of the present invention, a biaxial stretching blow-molding hot-parison method is commonly used. This method comprises feeding a parison obtained through an injection molding while its hot state, to a rcheating process without staying, followed by forming and thereafter, mechanically drawing the parison in a longitudinal direction while the parison is maintained at a constant temperature in a blow-die; and at the same time or in succession, blowing a pressed air into the blow-die so as to expand the parison in a circular direction (or in a transverse direction). Furthermore, there is a method of forming an aerosol container which comprises forming the engaged region of the valve cap on the periphery of the opening according to a non-stretching injection molding; and forming a body of the container which is filled with contents, according to a stretch blow-molding. According to such a stretch blow-molding, the longitudinal drawing of the body and the transverse drawing thereof are controlled to a low stretch ratio of 1.00 to 1.15 times and 1.90 to 2.20 times, respectively, and thereby, the container can be deformed and expanded under a high pressure following a temperature elevation of the contents and thus, the thickness thereof can be thinned so as to lower the internal pressure.
- With respect to the contents which an aerosol container of the present invention can be filled with, conventionally known ones can be employed. As the contents, for example, human-body articles, domestic articles, industrial articles can be exemplified. As for human-body articles, there are hair articles, cosmetics, odor-removing/sweat-repressing agents and other human-body articles; as for domestic articles, there are insecticides, coating agents, cleaners, foods and other domestic articles; and as for industrial articles, there are automobile articles and other industrial articles. As for the above-mentioned hair articles, there are hairsetting sprays, hairdressing conditioners, hair shampoos, rinses, acid wool-dyeing agents, oxidizing two-agent type permanent wool-dyeing agents, color sprays, decoloring agents, permanent-wave agents, hair-growing agents and the like. As cosmetics, there are shaving creams, aftershave lotions, perfumes, eau de Cologne, face-cleansing agents, anti-suntan agents, foundations, dehairing/decoloring agents, bath agents, dentifrice agents and the like. As the odor-removing/sweat-repressing agents, there are odor-removing agents, sweat-repressing agents, body shampoos and the like. As other human-body articles, there are muscle-antiflash agents, skin-trouble agents, medicines for a dermatophytosis, other medicines, injurious-insect repellents, cooling agents, cleaning-wiping agents, agents for oral-cavity and the like. As insecticides, there are space insecticides, insecticides for a cockroach, gardening insecticides, insecticides for a tick, insecticides for an uncomfortable insect and the like. As coating agents, there are domestic paints, automobile paints, undercoating agents and the like. As cleaners, there are domestic cleaners for glass, lens cleaners, carpet cleaners, bath cleaners, lustering cleaners for a floor/furniture, shoe/leather cleaners, wax lustering agents and the like. As other domestic articles, there are indoor odor-removing agents, toilet odor-removing agents, waterproofing agents, washing starches, herbicides, clothing insecticides, flameproofing agents and the like. As automobile articles, there are defogging agents, thawing agents, engine-starting agents, puncture-repairing agents, engine cleaners and the like. As other industrial articles, there are lubricating/anti corrosive agents, adhesive agents, metal deep-cut agents, mold releasing agents and the like.
- As the forms of the above-mentioned contents, a liquid, a fluid state, a semi-solid state, a foam state, a gaseous state, as well as a mixture of each of the above-mentioned states and a little solid in a powder state or a particle state, and the like can be properly selected and employed.
- The above-mentioned contents can include a material which has been conventionally employed as an additive agent. As such an additive agent, alcohol; a synthetic resin; a propellant (a simple substance selected from the group consisting of LPG (liquefied petroleum gas), DME (dimethyl ether), N2 CO2 and the like, or a mixture thereof); cellulose; ammonium; water; perfumes; dyes; surface active agents; pigments are properly selected and added thereto. For example, some of the above-mentioned hair sprays include a denatured alcohol and LPG for the propellant as main components, to which an acrylic resin alkanolamine liquid, polyoxyethyleneoleyl ether, a perfume and the like are added, while some of the above-mentioned hair treatments include the denatured alcohol and LPG for the propellant as main components, to which a liquid paraffin, propylene glycol, methylphenyl polysiloxane and a perfume are added.
- Hereinafter, Working Examples of the present invention will be in detail explained referring to the Drawings and Tables.
- An aerosol container shown in Figure 1 has a content volume of 97ml and a weight of 30g, wherein reference numeral (10) is an opening of the aerosol container, which is an engagement region for engaging a valve cap (which is not shown in Figure 1), and reference numeral (11) is a body for retaining contents therein. The aerosol containers were formed according to a biaxial stretching blow-molding hot-parison method, after mixing PET and PAr in mixing ratios as shown in Table 1. As the stretching conditions in the parison, a preheating temperature of 140 °C to 165°C and a heating time of 20 seconds were employed at a heating position, while a blow-die temperature of 20°C, a blow-pressure of 20 to 35kgf/cm2 and a blow-time of 10 to 15 seconds were employed at a stretching position. The stretch ratio of the body of each of bottles were 1.1 times in the longitudinal direction and 2.0 times in the transverse direction.
- With respect to the item "Evaluation at Temperature Elevated to 80°C " in Table 1, each of the aerosol containers was filled with contents and an aqueous solution containing LPG (liquefied petroleum gas) under the conditions of an ordinary temperature (about 25°C ) and an internal pressure of 6kg/cm2 and then, a valve cap as shown in Figure 2 was fitted into the opening. Supposing the inside of an automobile car as parked under the blazing sun, an environmental temperature was elevated from an ordinary temperature (about 25 °C ), and after the temperature reached 80°C, the temperature of 80°C was maintained for a period of eight hours, and then it was visually evaluated whether an engagement region which is positioned on the periphery of the opening of each of the aerosol containers had been broken or not.
- The composition of contents used here are as follows:
<Hair Spray> Weight% Acrylic Resin Alkanolamine Liquid (3%) 4.00 Polyoxyethyleneoleyl Ether 0.01 Triethanolamine 0.50 Perfume 0.17 Denatured Ethyl Alcohol of 99% 55.32 LPG 40.00 100.00 PET wt.% PAr wt.% Glass Transition Temperature Evaluation at Temperature Elevated to 80°C Comparative Examples 1 100 0 73 Engagement Region was Broken at 75°C in Middle of Elevation Working Examples 1 95 5 75 Not Broken 2 88 12 78 Not Broken 3 80 20 81 Not Broken 4 68 32 88 Not Broken 5 60 40 95 Not Broken Comparative Examples 2 50 50 102 Occurrence of Burst at Container Bottom - As shown in Table 1, when the ratio of PET:PAr by weight % is in the range of 60:40 to 95:5, the above-mentioned engagement region was not broken, and the containers were not burst as well, while when the ratio of a polyarylate is 50% (Comparative Example 2), the container's bottom having a low pressure-resistance was bursted.
- Aerosol containers which were produced in the same mixing ratios as the ones in the Comparative Example 1 and Working Example 1 were filled with the same contents under an internal pressure of 6 kg/cm2, respectively, and the environmental temperature was elevated. At this time, the temperature of vapor phase in the aerosol containers, the temperature of liquid-phase in the aerosol containers, the internal pressure in the aerosol containers, and the visual evaluation as to whether the engagement regions were broken are shown in Table 2.
PET/PAr Mixing Ratio Temperature-Elevating Time (min.) Environmental Temperature (°C) Vapor-Phase Temperature (°C) Liquid-Phase Temperature (°C) Internal Pressure (kg/cm2) Evaluation of Engagement Region Comparative Example 3 0 33 29 25 6.2 All Right 70 75 69 57 13.3 All Right 75 76 71 59 12.3 Engagement Region was Broken Working Example 6 0 36 35 33 6.9 All Right 70 72 65 57 12.8 All Right 80 76 71 61 13.6 All Right 90 80 75 66 10.8 All Right 120 80 76 73 5.5 All Right - As shown in Table 2, the engagement region was not broken by using a aerosol container-forming raw material composed of a mixture of polyarylate with polyethylene terephthalate, even if a vapor-phase temperature is 71°C, and an internal pressure is in the range of 12 to 13kg/cm2. This is, because the container was expanded in itself, and its thickness was thinned, and thereby, the internal pressure was decreased.
- According to the present invention, an aerosol container in which a valve cap is fitted into an opening of the container, is produced to have a glass transition temperature of a raw material of the aerosol container in the range of 74 °C to 100°C, and thereby, such an effect that the aerosol container in itself maintains a high pressure resistance, while even if the internal pressure of the aerosol container is increased, the valve cap or the contents there of are not explosively scattered out of the container can be provided.
Claims (5)
- An aerosol container in which a valve cap (7) is fitted into an opening (10) at the neck of the container, characterised in that the raw material for forming said aerosol container is a high molecular compound having a glass-transition temperature of 74° C to 100° C.
- The aerosol container according to claim 1, wherein said high molecular compound is selected from the group consisting of polycarbonate, poly(ethylene naphthalate), polysulfone, polyethersulfone, and a mixture of polyethylene terephthalate and polyarylate.
- The aerosol container according to claim 1, wherein said high molecular compound is a mixture of polyethylene terephthalate and polyarylate.
- The aerosol container according to claim 3, wherein a mixing ratio of a mixture of polyethylene terephthalate and polyarylate by weight % is in the range of 60:40 to 95:5.
- An aerosol container according to claim 1, wherein the body (11) of said aerosol container is formed under the conditions of a longitudinal drawing of 1.00 to 1.15 times, and a transverse drawing of 1.90 to 2.20 times according to a stretch blow-molding.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12179797A JP3807568B2 (en) | 1997-04-24 | 1997-04-24 | Aerosol container |
| JP12179797 | 1997-04-24 | ||
| JP121797/97 | 1997-04-24 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0873946A1 EP0873946A1 (en) | 1998-10-28 |
| EP0873946B1 true EP0873946B1 (en) | 2001-07-04 |
Family
ID=14820163
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19980107302 Expired - Lifetime EP0873946B1 (en) | 1997-04-24 | 1998-04-22 | Aerosol container |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0873946B1 (en) |
| JP (1) | JP3807568B2 (en) |
| DE (1) | DE69801022T2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9986809B2 (en) | 2013-06-28 | 2018-06-05 | The Procter & Gamble Company | Aerosol hairspray product comprising a spraying device |
| US10131488B2 (en) | 2015-06-01 | 2018-11-20 | The Procter And Gamble Company | Aerosol hairspray product comprising a spraying device |
| US10426979B2 (en) | 2011-09-15 | 2019-10-01 | The Procter And Gamble Company | Aerosol hairspray product for styling and/or shaping hair |
| US12128118B2 (en) | 2021-07-29 | 2024-10-29 | The Procter & Gamble Company | Aerosol dispenser containing a hairspray composition and a nitrogen propellant |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2784081B1 (en) * | 1998-10-06 | 2000-12-01 | Oreal | AEROSOL DISPENSER COMPRISING A SPHERICAL TANK IN PLASTIC MATERIAL |
| DE10031136A1 (en) * | 1999-07-01 | 2001-01-04 | Wella Ag | Pressurized gas container for dispensing hair dyes is of blow-molded polyethylene terephthalate or polyethylene naphthalate with specified dimensions to give high strength |
| FR2877926B1 (en) * | 2004-11-16 | 2007-01-26 | Oreal | PRESSURIZED DEVICE FOR HAIRSTAPING CAPILLARY FIBERS AND USE OF SUCH A DEVICE FOR THE SHAPING AND / OR CARE OF CAPILLARY FIBERS. |
| US20070292641A1 (en) | 2006-06-16 | 2007-12-20 | Gene Michael Altonen | Non-round plastic pressurized dispenser |
| FR3019803B1 (en) | 2014-04-10 | 2016-12-23 | Fareva | AEROSOL GENERATOR OF PLASTIC MATERIAL |
| CH712902A1 (en) * | 2016-09-12 | 2018-03-15 | Alpla Werke Alwin Lehner Gmbh & Co Kg | Internal pressure resistant plastic container, in particular plastic aerosol container. |
| KR102085477B1 (en) * | 2019-04-22 | 2020-03-05 | 필립산업(주) | Vessel for bov |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6376993A (en) * | 1986-09-19 | 1988-04-07 | Toyo Seikan Kaisha Ltd | Body structure of pressure container and manufacture thereof |
| JP2562343B2 (en) * | 1988-02-23 | 1996-12-11 | 北海製罐株式会社 | Aerosol container and aerosol product |
| FR2743356B1 (en) * | 1996-01-10 | 1998-02-13 | Oreal | LIQUID CONSISTENCY PRODUCT DEVICE WITH PASTE COMPRISING A SECURITY DEVICE |
-
1997
- 1997-04-24 JP JP12179797A patent/JP3807568B2/en not_active Expired - Lifetime
-
1998
- 1998-04-22 DE DE1998601022 patent/DE69801022T2/en not_active Expired - Lifetime
- 1998-04-22 EP EP19980107302 patent/EP0873946B1/en not_active Expired - Lifetime
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10426979B2 (en) | 2011-09-15 | 2019-10-01 | The Procter And Gamble Company | Aerosol hairspray product for styling and/or shaping hair |
| US11311749B2 (en) | 2011-09-15 | 2022-04-26 | The Procter And Gamble Company | Aerosol hairspray for styling and/or shaping hair |
| US9986809B2 (en) | 2013-06-28 | 2018-06-05 | The Procter & Gamble Company | Aerosol hairspray product comprising a spraying device |
| US10131488B2 (en) | 2015-06-01 | 2018-11-20 | The Procter And Gamble Company | Aerosol hairspray product comprising a spraying device |
| US12128118B2 (en) | 2021-07-29 | 2024-10-29 | The Procter & Gamble Company | Aerosol dispenser containing a hairspray composition and a nitrogen propellant |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69801022D1 (en) | 2001-08-09 |
| EP0873946A1 (en) | 1998-10-28 |
| JPH10297686A (en) | 1998-11-10 |
| DE69801022T2 (en) | 2001-11-15 |
| JP3807568B2 (en) | 2006-08-09 |
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