EP1035157B1 - Highly clean porous polyvinyl acetal resin, method for preparing the same, and method for storing the same - Google Patents
Highly clean porous polyvinyl acetal resin, method for preparing the same, and method for storing the same Download PDFInfo
- Publication number
- EP1035157B1 EP1035157B1 EP97913421A EP97913421A EP1035157B1 EP 1035157 B1 EP1035157 B1 EP 1035157B1 EP 97913421 A EP97913421 A EP 97913421A EP 97913421 A EP97913421 A EP 97913421A EP 1035157 B1 EP1035157 B1 EP 1035157B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- vinyl acetal
- resin body
- high degree
- cleanliness
- porous poly
- 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
- 229920002554 vinyl polymer Polymers 0.000 title claims abstract description 34
- 229920006324 polyoxymethylene Polymers 0.000 title claims abstract description 32
- 238000000034 method Methods 0.000 title claims description 67
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 title abstract description 3
- 239000011354 acetal resin Substances 0.000 title abstract 2
- 238000004140 cleaning Methods 0.000 claims abstract description 53
- 239000002245 particle Substances 0.000 claims abstract description 14
- 239000001301 oxygen Substances 0.000 claims description 117
- 229910052760 oxygen Inorganic materials 0.000 claims description 117
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 116
- 230000003749 cleanliness Effects 0.000 claims description 58
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 56
- 230000002745 absorbent Effects 0.000 claims description 34
- 239000002250 absorbent Substances 0.000 claims description 34
- 239000003795 chemical substances by application Substances 0.000 claims description 33
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 31
- 230000004888 barrier function Effects 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 17
- 238000004806 packaging method and process Methods 0.000 claims description 14
- 238000010894 electron beam technology Methods 0.000 claims description 12
- 230000005251 gamma ray Effects 0.000 claims description 8
- 230000035699 permeability Effects 0.000 claims description 6
- 229910001415 sodium ion Inorganic materials 0.000 claims description 6
- 150000002500 ions Chemical class 0.000 claims description 4
- 230000001678 irradiating effect Effects 0.000 claims description 3
- 238000005406 washing Methods 0.000 abstract description 5
- 238000010828 elution Methods 0.000 abstract description 2
- 239000011347 resin Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000012535 impurity Substances 0.000 abstract 1
- 238000002203 pretreatment Methods 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 41
- -1 poly(vinyl alcohol) Polymers 0.000 description 20
- 239000004698 Polyethylene Substances 0.000 description 10
- 238000011109 contamination Methods 0.000 description 10
- 229920000573 polyethylene Polymers 0.000 description 10
- 238000005259 measurement Methods 0.000 description 9
- 239000004065 semiconductor Substances 0.000 description 8
- 239000007789 gas Substances 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000011148 porous material Substances 0.000 description 7
- 230000008859 change Effects 0.000 description 6
- 238000000691 measurement method Methods 0.000 description 5
- 238000009928 pasteurization Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 230000000903 blocking effect Effects 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 229910021642 ultra pure water Inorganic materials 0.000 description 4
- 239000012498 ultrapure water Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000008399 tap water Substances 0.000 description 3
- 235000020679 tap water Nutrition 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 2
- 244000052616 bacterial pathogen Species 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000011538 cleaning material Substances 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 150000002926 oxygen Chemical class 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 238000012858 packaging process Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000004321 preservation Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- OSDLLIBGSJNGJE-UHFFFAOYSA-N 4-chloro-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1Cl OSDLLIBGSJNGJE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- 239000004288 Sodium dehydroacetate Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000005443 coulometric titration Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940079839 sodium dehydroacetate Drugs 0.000 description 1
- 235000019259 sodium dehydroacetate Nutrition 0.000 description 1
- DSOWAKKSGYUMTF-GZOLSCHFSA-M sodium;(1e)-1-(6-methyl-2,4-dioxopyran-3-ylidene)ethanolate Chemical compound [Na+].C\C([O-])=C1/C(=O)OC(C)=CC1=O DSOWAKKSGYUMTF-GZOLSCHFSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 238000009461 vacuum packaging Methods 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B08—CLEANING
- B08B—CLEANING IN GENERAL; PREVENTION OF FOULING IN GENERAL
- B08B1/00—Cleaning by methods involving the use of tools
- B08B1/10—Cleaning by methods involving the use of tools characterised by the type of cleaning tool
- B08B1/14—Wipes; Absorbent members, e.g. swabs or sponges
Definitions
- This invention relates to a porous poly (vinyl acetal) resin body and a process of preparing the same, and a method of storing the same, more specifically, the method of preparing and storing the porous body in a state where the body is wet and is free of contamination with organic substances, dissolved ions, and fine particles and free of contamination with a freeminor raw material and a major rawmaterial, i.e., poly(vinyl alcohol)added in the production processes of the porous poly (vinyl acetal) resin body, and agents added for the purposes of pasteurizing and moldproofing the porous poly (vinyl acetal) resin body .
- a porous poly (vinyl acetal) resin body is well known as a material having excellent water-absorbing and water-holding properties and showing, in a wet state, a desirable flexibility and an impact strength. With these properties, the porous poly (vinyl acetal) resin body is widely used as an optimum material for cleaning tools and wipers. Especially, because the body has a hydrophilic property and an excellent cleaning capability, and nevertheless does not damage objects scrubbed and, in addition, is excellent in strength, it has wide industrial applications such as cleaning of clean rooms, semiconductors, and electronic parts, and also plays an important role as a water absorbent material.
- porous poly(vinyl acetal) resin body herein is also called poly(vinyl acecal) sponge and will be abbreviated as "PVAt sponge” hereinafter.
- a PVAt sponge is the most suitable material for cleaning clean rooms.
- the PVAt sponge should generally be used in a wet state, because the PVAt sponge hardens and loses its softness and elasticity, when dried.
- a water absorption rate of a porous PVAt body in a dry state is very different from that in a wet state, with the former being significantly slower than the latter. It takes much time to change the sponge from a dry state to a wet state, and therefore, it is practically preferred to keep it wet without drying it.
- porous PVAt type body tends to get moldy when kept wet for a long time. Mold causes problems in regard of hygiene, appearance and handling and, therefore, it is necessary to provide a porous PVAt type body with a moldproofing property.
- the PVAt sponge In storing the PVAt sponge, contamination of the porous body with organic substances, ionic substances, fine particles, and microorganisms shall be prevented. Especially in applications in the semiconductor industry, these contaminants should be reduced to the lowest possible limit.
- an agent having moldproofing and pasteurizing properties such as an aqueous solution of sodium dehydroacecate, 4-chloro-3, 5-dimethylphenol, benzalconium chloride, and benzimidazol.
- the PVAt sponge treated with a solution comprising those agents and stored is used as such for cleaning semiconductors or the like, these agents are eluted in cleaning water, i.e., ultra-pure water used for and contaminate the cleaning water and subjects to be cleaned.
- cleaning water i.e., ultra-pure water used for and contaminate the cleaning water and subjects to be cleaned.
- the PVAt sponge is usually subjected to a long time of pre-cleaning before used.
- a PVAt sponge is used as a cleaning material in the semiconductor industry or used as a water absorbent material in the electronics industry, for example, cleaning materials for precision cleaning of silicon wafers and photomasks, or for cleaning of printed circuit boards and lead frames or used as a water absorbent
- foreign elements eluted from the PVAt sponge not only degrade qualities of products but also contaminate the production systems and environment itself, causing a huge damage.
- the foreign elements originated from the porous body should be reduced extremely, but the above-mentioned storing method using agents could not meet this requirement.
- the purpose of the present invention is to provide a PVAt sponge having a high degree of cleanliness , a method of preparing the same and a method of storing the same which allows strict preservation and easy handling of the cleanliness of the PVAt sponge having a high degree of cleanliness.
- the present inventions are a PVAt sponge having a high degree of cleanliness, a method of preparing a PVAt sponge having a high degree of cleanliness by cleaning the PVAT sponge with pure water from which foreign substances dissolved or floating in water such as particles, ions and organic substances have been removed, and a method of storing the same by hermetically packaging the thus prepared PVAt sponge having a high degree of cleanliness as a whole together with an oxygen absorbent with an oxygen barrier film.
- the present PVAt sponge with a high degree of cleanliness is characterized by such a cleanliness that COD (Chemical Oxygen Demand) is 5 ppm or less
- the high degree of cleanliness of the forms PVAt sponge may also be characterised by and a concentration of Sodium ions of 1 ppm or less a conductivity is 5 ⁇ S/cm or lower, and the number of particles having a size of 2.5 ⁇ m or less is 50,000/cc or smaller.
- the present sponge with a high degree of cleanliness allows one to reduce or eliminate conventionally required pre-cleaning, for example, a thorough cleaning to prevent foreign substances from being eluted, before used in a washing step in a clean room. Further, by increasing the degree of cleanliness, the sponge can be used in severer environmental conditions such as those in a semiconductor production process.
- the present method of preparing the PVAt sponge with a high degree of cleanliness is characterized by cleaning the sponge with pure water from which foreign substances dissolved or floating in water such as particles, ions and organic substances have been removed, and also characterized in that the pure water used for cleaning has a conductivity of 0.1 ⁇ S/cm or lower and COD of 1 ppm or less.
- the above-mentioned cleaning with pure water is preferably carried out in an environment where a higher degree of cleanliness chan Class 100 specified in the Federal Standards 209D is maintained.
- the present method for the preparation enables one to prepare a sponge with a high degree of cleanliness.
- By increasing the degree of cleanliness of pure water used for the preparation it is possible to prepare a PVAt sponge with a higher degree of cleanliness which can be used in severer environmental conditions such as those in a semiconductor production process.
- the present method of storing a sponge with a high degree of cleanliness is characterized by hermetically packaging the whole PVAt sponge prepared with a high degree of cleanliness wi th an oxygen barrier film together with an oxygen absorbent.
- the above-mentioned oxygen barrier film is characterized by an oxygen permeability of 200 cc/m 2 ⁇ atm ⁇ 24 hrs or smaller. Using a material having such an excellent oxygen blocking property produces a state with a low oxygen concentration which is almost oxygen free.
- an oxygen detecting agent is contained in the hermetic package.
- the hermetic package By using this manner of packaging, one candetect the presence of oxygen in case, for example, where the package is partly torn to break the seal, to thereby prevent erroneous use of an inferior product.
- a method of increasing the degree of cleanliness for storing a PVAt sponge with a high degree of cleanliness is characterized by hermetically packaging the PVAt sponge with a high degree of cleanliness, and then irradiating the package with an electron beam or ⁇ -ray.
- This method can strictly maintain the cleanliness of the sponge with a high degree of cleanliness without a moldproofing agent. Further, less mold grows even in the presence of oxygen because the PVAt sponge is pasteurized by the irradiation with an electron beam or ⁇ -ray. Accordingly, any packaging material can be used as long as it can make hermetic package.
- a method of storing a sponge with a high degree of cleanliness is provided which sponge can be used with very simple pretreatment before use.
- an irradiation dosage of an electron beam or ⁇ -ray By setting an irradiation dosage of an electron beam or ⁇ -ray to 10 kGy or smaller, changes in physical properties of the sponge can be suppressed to be extremely small. If the irradiation dosage is larger, a compression stress of the sponge, for instance, increases, and thus the sponge becomes harder.
- an oxygen content in the sealed package is made low before the irradiation with an electron beam or ⁇ -ray. This is because the electron beam or ⁇ -ray irradiation activates oxygen and the activated oxygen may degrade the sponge. Therefore, it is preferred to hermetically package the sponge together with an oxygen absorbent with an oxygen barrier film. Further, an oxygen permeability of the oxygen barrier film is preferably 200 cc/m 2 ⁇ atm ⁇ 24 hrs or smaller. By doing so, the oxygen content in the package can be kept extremely low and changes in physical properties of the sponge can be suppressed further.
- the sponge is covered by a molded sheet article before packaged. This prevents the sponge from deforming when an internal pressure in the package become sub-atmospheric by an oxygen absorbent. Also it prevents deformation by an external pressure.
- Still preferred is double packaging by covering the hermetic package with a film. This allows one to reduce contamination of an environment where the sponge is used, just by discarding the outer package when using the sponge.
- the packaging process is more preferably carried out in an environment where a higher degree of cleanliness than Class 100 specified in the Federal Standards 209D is maintained.
- a higher degree of cleanliness required for the use in much severer requirement for environment can be maintained.
- a PVAt sponge is widely used for cleaning applications in clean rooms, cleaning semiconductors, and cleaning electronic parts, and used as water absorbent. It is beneficial to apply the present sponge with a high degree of cleanliness, the present method of preparing the same and the method of storing the same to those applications and to a cleaning sponge roller.
- pure water used in the present invention preferably has such water quality that a conductivity at 25°C is 0.1 ⁇ S/cm or lower, total organic carbon is 1 ppm or less, the number of particles having a size of 0.3 ⁇ m or bigger is 100/ml or smaller, and the number of living germs is 10/ml or smaller, and more preferably has such water quality that a conductivity at 25°C is 0.055 ⁇ S/cm or lower, total organic carbon is 1 ppm or less, the number of particles having a size of 0.1 ⁇ m or bigger is 1/ml or smaller, and the number of living germs is 0.01/ml or smaller.
- ultra-pure water By cleaning the PVAt sponge with the ultra-pure water having the above water quality, foreign elements adhered on the porous body are removed effectively.
- ultra-pure water can be prepared by normal filtration, by using a precision filtration membrane, an ultrafiltration membrane, a reverse osmosis membrane or a dialysis membrane, by ion exchanging, or by any combination thereof.
- the degree of cleanliness of the PVAt sponge obtained by cleaning with the above-mentioned ultra-pure water is such that a conductivity is 5 ⁇ S/cm or lower, COD is 5 ppm or less, Na + ion concentration is 1 ppm or lower, and the number of particles having a size of 2.5 ⁇ m or smaller is 50, 000/cc or smaller.
- the conductivity and the Na + ion concentration are those in the water adhered on the sponge. COD is determined on pure water in which the PVAt sponge was crumpled and squeezed.
- poly(vinylidene chloride), nylon, poly(vinylacetate), poly(vinyl alcohol), aluminum foils, or aluminum deposited films can be preferably used. More preferably, films having an oxygen permeability of 10 cc/m 2 ⁇ atm ⁇ 24hrs at 20-25°C or lower are used. A laminated film consisting of two or more of these films having a high oxygen blocking property or a combination of the above-mentioned oxygen barrier film layered on a film such as a polyethylene, polyester, or polypropylene film are more preferred also for mechanical strength.
- an oxygen barrier film as that used for the inner package can be used, but an oxygen permeating film can be used such as widely used materials, such as polyethylene, polypropylene, polyester, and nylon.
- an oxygen permeating film can be used such as widely used materials, such as polyethylene, polypropylene, polyester, and nylon.
- oxygen absorbent contained in the package made of a material with a high oxygen blocking property substances which are chemically oxidized with ease can be used, for example, ascorbic acid, active metal powder, and sulfites, among which iron type substances are preferred in regard of their handling property, oxygen absorbing rate and oxygen absorbing capacity.
- an oxygen absorbent in a form of fine powder to achieve a higher reactivity with oxygen.
- the oxygen absorbent fine powder is used with being wrapped in a material having smaller pores than a diameter of the oxygen absorbent and a gas permeability.
- the PVAt sponge in the package can maintain for a long time the degree of cleanliness attained immediately after the cleaning with pure water.
- Irradiating the packaged PVAt sponge with an electron beam or ⁇ -ray sterilizes the PVAt sponge, so that mold growth can be prevented even when oxygen exists more or less.
- any packaging material may be used satisfactorily as long as it can make a hermetic package and there is no need to use an oxygen barrier film. As a result, package and packaging procedure can be simplified.
- a PVAt sponge prepared by reacting PVA with formalin is cleaned thoroughly with water for general use to wash away reaction residues, unreacted substances, and additives. Then, the sponge is soaked in pure water having the aforesaid quality and subjected to mechanical stretching and compression. Subsequently, water contained in the sponge is squeezed out sufficiently and then the sponge is allowed to absorb another pure water, followed by the above procedures.
- the thus-cleaned PVAt sponge wet with pure water is covered as a whole with an oxygen barrier film and sealed completely.
- An oxygen absorbent is contained in the package together with the PVAt sponge.
- An oxygen detecting agent may also be contained.
- the whole PVAt sponge may be covered with a molded sheet article and then hermetically packaged as a whole with an oxygen barrier film.
- the inner pressure in the package become sub-atmospheric, which causes the contained PVAt sponge to be deformed. If the deformation is kept for a long time, there may be a problem that the deformed part does not recover the original shape. This problem can be avoided by covering the whole PVAt sponge with a relatively hard, molded sheet article as described above.
- contamination of environment where a sponge is used can be reduced further by double packaging a PvAt sponge packaged in an oxygen barrier film with a film, and discarding the outer package when the PVAT sponge is used.
- the present method can be applied not only to a porous material which hardens on drying but also to materials made of other polymers.
- the present method can be applied to rubbery materials such as NBR and SBR and fibrous materials such as unwoven fabrics to prevent degradation of the materials themselves by oxidation or to preserve performances of agents added to the materials.
- cleaning a PVAt sponge and storing the sponge according to the present invention allows one to store the porous body in a wet state for a long period of time without contamination by fine particles, organic substances, ionsor the like and also without contamination by a moldproofing agent.
- the present invention allows one to reduce or eliminate pre-cleaning which was conventionally practiced before using a PVAt sponge.
- the PVAt sponge is stored in an oxygen-free atmosphere for a long time and consequently mold growth and quality change of the porous body itself by oxidation can be prevented. Further, the present method can be applied widely to materials of which degradation by oxidation and quality change must be prevented, besides porous materials or wet materials.
- a water sample is prepared by crumpling and squeezing 100cc of a sponge 100 times in 400 cc of distilled water and diluting it to 500 cc with tap water.
- Measurement method the amount of potassium permanganate required to oxidize organic substances in the water sample is determined by coulometric titration and the amount is reduced to the equivalent amount of oxygen.
- Measurement instrument portable, speedy type COD meter, HC-507, ex Central Kagaku Co.
- a water sample is prepared by squeezing a sponge which has been impregnated with a sufficient amount of DI water and allowed to stand for about 3 minutes.
- Measurement method electrodes are immersed in the sample and a conductivity is measured in an AC bipolar method.
- Measurement instrument compact conductivity meter, B-173 type, ex Horiba Seisakusho Co.
- a water sample is prepared by crumpling and squeezing 10cc of a sponge 100 times in 800 cc of tap water and diluting it to 1000 cc with tap water.
- Measurement method a size of each particle in 10 cc of the sample is determined by voltage drop caused by cut-off of halogen light and the number of the particle is counted in a particle counter of a light cut-off type.
- Measurement instrument HIAC/ROYCO, MODEL4100
- a water sample is prepared by squeezing a sponge which has been impregnated with a sufficient amount of DI water and allowed to stand for about 3 miniutes.
- Measurement method the sample is dropped on a flat sensor of a sodium ion electrode.
- Measurement instrument compact Ion meter, CANDY C-122,ex Horiba Seisakusho Co.
- a sponge roller 1 made of poly(vinyl acetal) (PVAT) having an outer diameter cf 60mm, an inner diameter of 30 mm and a length of 254 mm was immersed in pure water having such water quality that its COD was 1 ppm, the conductivity at 25 °C was 0.06 ⁇ S/cm and the number of particles of 2.5 ⁇ or bigger was 0/ml.
- the sponge was forced to be stretched and compressed mechanically. Then, water contained in the sponge was squeezed out to remove the washing water. By repeating the above procedure with fresh pure water once again, the sponge was cleaned. After this cleaning, the wet sponge roller was placed in a package 2 of 450 mm by 170 mm made of an oxygen barrier film as shown in Fig. 1, an oxygen absorbent 3 and an oxygen detecting agent 4 were introduced, and then the opening was heat sealed to thereby completely seal the package.
- PVAT poly(vinyl acetal)
- the oxygen barrier film used consists of 4 layers as shown in Fig.2.
- the film consists of a top layer 5 of poly (vinylidene chloride), a second layer of nylon 6, a third layer of polyethylene 7 and a bottom layer of linear low density polyethylene 8, with the thickness of the layers being 5 ⁇ m. 10 ⁇ m, 25 ⁇ m, and 60 ⁇ m, respectively.
- As the oxygen absorbent Ageless FX-400, ex Mitsubishi Gas Co., was used .
- Ageless-eye KS ex Mitsubishi Gas Co.
- This sponge roller 1 is to be used for precision cleaning of aluminum disks or the like and, as shown in fig. 3, has many projections 9 on its surface. As shown in Fig.4, these projections 9 scrub and clean an object 10 to be cleaned such as aluminum disks or the like in the presence of water or the like when the sponge roller 1 is rotated.
- APVAt sponge roller was cleaned as in Example 1. After the cleaning, the wet sponge roller was placed in a package of 450 mm by 170 mm made of apolyechylene film and the opening was heat sealed to completely sael the package. This time, no oxygen absorbent and no oxygen detecting agent were introduced. The whole package was irradiated with an electron beam. Irradiation energy was 5 MeV and the dosage was 4kGy.
- a sponge roller of PVAt having an outer diameter of 60mn, an inner diameter of 30 mm and a length of 254 nm was wetted with the above-mentioned pure water, but no cleaning was applied.
- the roller was placed in a package of 450 mm by 170 mm made of an oxygen barrier film.
- the oxygen detecting agent was placed in the package, but no a oxygen absorbent was used and then the opening was heat sealed.
- the same kind of the oxygen barrier film as used in Example 1 was used.
- a sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was wetted with the above-mentioned pure water, but no cleaning was applied.
- the roller was placed in a package of 450 mm by 170 mm made of a polyethylene film.
- An oxygen absorbent and an oxygen detecting agent were also included and the opening was heat sealed. The same kinds of oxygen absorbent and the oxygen detecting agent as used in Example 1 were used.
- a sponge roller of PvAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was soaked in a mixture of 3,000 cc of a 0.3 wt% aqueous solution of sodium dehydroacetate and 3,000 cc of a 0.3 wt% aqueous solution of oxalic acid and a water content of the sponge roller was made equal to that in Example 1.
- the sponge roller was placed in the same kind of a polyethylene film package as used in Comparative Example 2 together with an oxygen detecting agent, but without an oxygen absorbent, and the package was sealed completely.
- the same kind of an oxygen detecting agent as used in Example 1 was used.
- a sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was wetted with the above-mentioned pure water, but no cleaning was applied.
- the roller was placed in a package of 450 mm by 170 mm made of an oxygen barrier film. Air in the package was evacuated and then, nitrogen gas was introduced. The oxygen detecting agent was also placed in the package without an oxygen absorbent and package was sealed completely. The same kind of oxygen barrier film as used in Example 1 was used.
- a sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was cleaned as in Example 1. Then, after the cleaning, the wet sponge was placed in a package of 450 mm by 170 mm made of a polyethylene film together with the oxygen absorbent and the oxygen detecting agent and the package was heat sealed completely at its opening. The same kind of a polyethylene film as used in Comparative Example 2 was used.
- a sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was cleaned as in Example 1. Then, after the cleaning, the wet sponge was placed in a package of 450 mm by 170 mm made of a polyethylene film together with the oxygen detecting agent, but without an oxygen absorbent, and the package was heat sealed completely at its opening.
- the same kind of a polyethylene film as used in Comparative Example 2 was used.
- the PVAt sponge rollers treated as described above were stored in a thermostatic room kept at 23 °C and change in appearance was observed for 200 - days. Appearances of the porous rollers. i.e., the degree of mold growth was as shown in the following Table 1.
- Example 2 the irradiation of an electron beam on the packaged sponge roller prevented mold growth for at least 200 days as in Example 1. This is achieved because the irradiation with an electron beam sterilizes the sponge roller to thereby prevent mold growth even when there is a little oxygen. This means that any package which can be sealed may be used satisfactorily and it is unnecessary to use an oxygen barrier film. Further, a package and a packaging process can be simpler.
- Comparative Example 3 in Table 1 shows, a conventional method where a moldproofing agent was used. Although mold did not grow, the purpose of the present invention could not be achieved.
- Comparative Examples 5 and 6 cleaning with pure water was carried out. In the both Examples, a polyethylene film was used but no oxygen barrier film was used. In Comparative Example 5, an oxygen absorbent was included, and accordingly the result is better than in the other Comparative Examples, but not as good as in the Examples. In Comparative Example 6, the result is worse than that of Comparative Example 5 because no oxygen absorbent was included.
- a PVAt sponge should be hermetically packaged together with an oxygen absorbent with an oxygen barrier film according to the present invention.
- mold growth can be restrained for an prolonged period of time by cleaning the PVAt sponge with pure water and keeping it in an oxygen-free or almost oxygen-free atmosphere.
- the amount of the eluted components come within the allowable range in a short period of cleaning.
- a longer cleaning period is necessary because cleaning with pure water was not conducted.
- Comparative Example 3 the conductivity is higher due to the eluted moldproofing agent.
- Table 3 shows whether oxygen was detected or not by the oxygen detecting agents contained in the packages.
- “none” means that the oxygen concentration was 0.1% or smaller.
- Example 1 the inside of the package was kept oxygen free for a long time. In contrast with it, in the Comparative Examples, the oxygen concentration could be maintained low for a short time in some cases, but not for a long time.
- Table 3 Presence of oxygen in the package days 10 days 30 days 60 days 100 days 200 days.
- Example 1 to store a PVAt sponge in a wet state, mold growth can be restrained for a long time by cleaning the PVAt sponge with pure water and keeping it in an oxygen-free or almost oxygen-free atmosphere.
- the present invention allows one to keep porous bodies oxygen-free for a long time and , therefore, can prevent change in quality of porous bodies by oxidation in addition to a moldproofing effect. Further, the present storing method can be used to store not only porous materials or wet materials but also those which should be protected from degradation by oxidation or quality change.
- Example 2 mold growth was prevented even in the presence of oxygen as far as the package was hermetic, because the sponge was sterilized by irradiation with an electron beam.
- the present storing method can greatly reduce the amount of eluted substances and dust from a PVAt sponge; can shorten or eliminate pretreatment such as washing before used; maintains the moldproofing effect for a long time even when storing the PVAt sponge in a wet state; and prevents degradation by oxidation or deterioration because the porous material is kept oxygen free. Therefore, the present method is extremely useful.
Landscapes
- Packages (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
- This invention relates to a porous poly (vinyl acetal) resin body and a process of preparing the same, and a method of storing the same, more specifically, the method of preparing and storing the porous body in a state where the body is wet and is free of contamination with organic substances, dissolved ions, and fine particles and free of contamination with a freeminor raw material and a major rawmaterial, i.e., poly(vinyl alcohol)added in the production processes of the porous poly (vinyl acetal) resin body, and agents added for the purposes of pasteurizing and moldproofing the porous poly (vinyl acetal) resin body .
- A porous poly (vinyl acetal) resin body is well known as a material having excellent water-absorbing and water-holding properties and showing, in a wet state, a desirable flexibility and an impact strength. With these properties, the porous poly (vinyl acetal) resin body is widely used as an optimum material for cleaning tools and wipers. Especially, because the body has a hydrophilic property and an excellent cleaning capability, and nevertheless does not damage objects scrubbed and, in addition, is excellent in strength, it has wide industrial applications such as cleaning of clean rooms, semiconductors, and electronic parts, and also plays an important role as a water absorbent material.
- The porous poly(vinyl acetal) resin body herein is also called poly(vinyl acecal) sponge and will be abbreviated as "PVAt sponge" hereinafter.
- A PVAt sponge is the most suitable material for cleaning clean rooms. To realize this advantage, the PVAt sponge should generally be used in a wet state, because the PVAt sponge hardens and loses its softness and elasticity, when dried. A water absorption rate of a porous PVAt body in a dry state is very different from that in a wet state, with the former being significantly slower than the latter. It takes much time to change the sponge from a dry state to a wet state, and therefore, it is practically preferred to keep it wet without drying it.
- However, the porous PVAt type body tends to get moldy when kept wet for a long time. Mold causes problems in regard of hygiene, appearance and handling and, therefore, it is necessary to provide a porous PVAt type body with a moldproofing property.
- In storing the PVAt sponge, contamination of the porous body with organic substances, ionic substances, fine particles, and microorganisms shall be prevented. Especially in applications in the semiconductor industry, these contaminants should be reduced to the lowest possible limit. In a conventional method of storing the PVAt sponge, the sponge is impregnated with an agent having moldproofing and pasteurizing properties, such as an aqueous solution of sodium dehydroacecate, 4-chloro-3, 5-dimethylphenol, benzalconium chloride, and benzimidazol.
- However, when the PVAt sponge treated with a solution comprising those agents and stored is used as such for cleaning semiconductors or the like, these agents are eluted in cleaning water, i.e., ultra-pure water used for and contaminate the cleaning water and subjects to be cleaned. To remove these agents from the PVAt sponge treated with a solution comprising those agents and stored, the PVAt sponge is usually subjected to a long time of pre-cleaning before used.
- In addition, when a PVAt sponge is created with those agents and stored, the porous body is changed in qualities or degraded by the effects of some agents, which is also a problem.
- Particularly, when a PVAt sponge is used as a cleaning material in the semiconductor industry or used as a water absorbent material in the electronics industry, for example, cleaning materials for precision cleaning of silicon wafers and photomasks, or for cleaning of printed circuit boards and lead frames or used as a water absorbent, foreign elements eluted from the PVAt sponge not only degrade qualities of products but also contaminate the production systems and environment itself, causing a huge damage. Thus, in applications in clean rooms or in an environment with a highly controlled cleanliness, the foreign elements originated from the porous body should be reduced extremely, but the above-mentioned storing method using agents could not meet this requirement.
- To deal with these problems, the following methods may be thought: autoclave pasteurization under heat and pressure; pasteurization with an oxidizing gas such as ethylene oxide and ozone; storing a product in a sealed container and replacing a gas in the container with an inert gas; and pasteurization with UV light. For other materials than the PvAt sponge, an appropriate method was properly selected and applied among those methods. However, none of the methods is suitable to the PVAt sponge. For example, in the autoclave pasteurization, the material itself shrinks and loses its softness and elasticity, peculiar to the PVAT sponge. In the pasteurization with an oxidizing gas, it is difficult for the gas to penetrate deeply into the porous body and the porous body itself tends to deteriorate by oxidation. In the method where a product is stored in a sealed container and a gas in the container is replaced with an inert gas, it is not easy to remove oxygen dissolved in water adhered on the porous body and in the body itself and, consequently, mold growth cannot be prevented completely. The method utilizing UV light is not practical because UV light affects only the surface of the porous body.
- As a result of intensive researches, the present inventor have found that, it is possible to prevent mold growth during prolonged storage of a PVAt sponge in a wet state and to avoid elution of substances or rising of dusts from the PVAt sponge in use after the storage to thereby reduce or eliminate a pre-cleaning process before use. The purpose of the present invention is to provide a PVAt sponge having a high degree of cleanliness , a method of preparing the same and a method of storing the same which allows strict preservation and easy handling of the cleanliness of the PVAt sponge having a high degree of cleanliness.
- The present inventions are a PVAt sponge having a high degree of cleanliness, a method of preparing a PVAt sponge having a high degree of cleanliness by cleaning the PVAT sponge with pure water from which foreign substances dissolved or floating in water such as particles, ions and organic substances have been removed, and a method of storing the same by hermetically packaging the thus prepared PVAt sponge having a high degree of cleanliness as a whole together with an oxygen absorbent with an oxygen barrier film.
- The present PVAt sponge with a high degree of cleanliness is characterized by such a cleanliness that COD (Chemical Oxygen Demand) is 5 ppm or less, the high degree of cleanliness of the forms PVAt sponge may also be characterised by and a concentration of Sodium ions of 1 ppm or less a conductivity is 5µ S/cm or lower, and the number of particles having a size of 2.5µm or less is 50,000/cc or smaller.
- The present sponge with a high degree of cleanliness allows one to reduce or eliminate conventionally required pre-cleaning, for example, a thorough cleaning to prevent foreign substances from being eluted, before used in a washing step in a clean room. Further, by increasing the degree of cleanliness, the sponge can be used in severer environmental conditions such as those in a semiconductor production process.
- The present method of preparing the PVAt sponge with a high degree of cleanliness is characterized by cleaning the sponge with pure water from which foreign substances dissolved or floating in water such as particles, ions and organic substances have been removed, and also characterized in that the pure water used for cleaning has a conductivity of 0.1 µ S/cm or lower and COD of 1 ppm or less.
- The above-mentioned cleaning with pure water is preferably carried out in an environment where a higher degree of cleanliness chan Class 100 specified in the Federal Standards 209D is maintained.
- The present method for the preparation enables one to prepare a sponge with a high degree of cleanliness. By increasing the degree of cleanliness of pure water used for the preparation, it is possible to prepare a PVAt sponge with a higher degree of cleanliness which can be used in severer environmental conditions such as those in a semiconductor production process.
- By increasing the degree of cleanliness of an environment where the cleaning is performed, one can prepare a sponge with a higer degree of cleanliness which can be used even when severer quality is required.
- The present method of storing a sponge with a high degree of cleanliness is characterized by hermetically packaging the whole PVAt sponge prepared with a high degree of cleanliness wi th an oxygen barrier film together with an oxygen absorbent.
- By storing an PVAt with a high degree of cleanliness together with an oxygen absorbent in a closed package having an oxygen-blocking property to thereby keep the inside of the package in an oxygen-free state or in a nearly oxygen-free state with a low oxygen concentration according to the present storing method, one can strictly maintain the cleanliness of the sponge with a high degree of cleanliness without a moldproofing agent and also reduce or eliminate the time required for a pretreatment before use.
- The above-mentioned oxygen barrier film is characterized by an oxygen permeability of 200 cc/m2·atm· 24 hrs or smaller. Using a material having such an excellent oxygen blocking property produces a state with a low oxygen concentration which is almost oxygen free.
- Preferably, an oxygen detecting agent is contained in the hermetic package. By using this manner of packaging, one candetect the presence of oxygen in case, for example, where the package is partly torn to break the seal, to thereby prevent erroneous use of an inferior product.
- A method of increasing the degree of cleanliness for storing a PVAt sponge with a high degree of cleanliness is characterized by hermetically packaging the PVAt sponge with a high degree of cleanliness, and then irradiating the package with an electron beam or γ-ray. This method can strictly maintain the cleanliness of the sponge with a high degree of cleanliness without a moldproofing agent. Further, less mold grows even in the presence of oxygen because the PVAt sponge is pasteurized by the irradiation with an electron beam or γ-ray. Accordingly, any packaging material can be used as long as it can make hermetic package. A method of storing a sponge with a high degree of cleanliness is provided which sponge can be used with very simple pretreatment before use.
- By setting an irradiation dosage of an electron beam or γ -ray to 10 kGy or smaller, changes in physical properties of the sponge can be suppressed to be extremely small. If the irradiation dosage is larger, a compression stress of the sponge, for instance, increases, and thus the sponge becomes harder.
- Preferably, an oxygen content in the sealed package is made low before the irradiation with an electron beam or γ-ray. This is because the electron beam or γ-ray irradiation activates oxygen and the activated oxygen may degrade the sponge. Therefore, it is preferred to hermetically package the sponge together with an oxygen absorbent with an oxygen barrier film. Further, an oxygen permeability of the oxygen barrier film is preferably 200 cc/m2·atm·24 hrs or smaller. By doing so, the oxygen content in the package can be kept extremely low and changes in physical properties of the sponge can be suppressed further.
- Preferably, the sponge is covered by a molded sheet article before packaged. This prevents the sponge from deforming when an internal pressure in the package become sub-atmospheric by an oxygen absorbent. Also it prevents deformation by an external pressure.
- Still preferred is double packaging by covering the hermetic package with a film. This allows one to reduce contamination of an environment where the sponge is used, just by discarding the outer package when using the sponge.
- The packaging process is more preferably carried out in an environment where a higher degree of cleanliness than Class 100 specified in the Federal Standards 209D is maintained. By packaging in such an environment, a higher degree of cleanliness required for the use in much severer requirement for environment can be maintained.
- As described above, a PVAt sponge is widely used for cleaning applications in clean rooms, cleaning semiconductors, and cleaning electronic parts, and used as water absorbent. It is beneficial to apply the present sponge with a high degree of cleanliness, the present method of preparing the same and the method of storing the same to those applications and to a cleaning sponge roller.
- To explain the present invention in more detail, pure water used in the present invention preferably has such water quality that a conductivity at 25°C is 0.1µ S/cm or lower, total organic carbon is 1 ppm or less, the number of particles having a size of 0.3µm or bigger is 100/ml or smaller, and the number of living germs is 10/ml or smaller, and more preferably has such water quality that a conductivity at 25°C is 0.055µ S/cm or lower, total organic carbon is 1 ppm or less, the number of particles having a size of 0.1µ m or bigger is 1/ml or smaller, and the number of living germs is 0.01/ml or smaller. By cleaning the PVAt sponge with the ultra-pure water having the above water quality, foreign elements adhered on the porous body are removed effectively. Such ultra-pure water can be prepared by normal filtration, by using a precision filtration membrane, an ultrafiltration membrane, a reverse osmosis membrane or a dialysis membrane, by ion exchanging, or by any combination thereof.
- The degree of cleanliness of the PVAt sponge obtained by cleaning with the above-mentioned ultra-pure water is such that a conductivity is 5µ S/cm or lower, COD is 5 ppm or less, Na+ ion concentration is 1 ppm or lower, and the number of particles having a size of 2.5 µ m or smaller is 50, 000/cc or smaller. These figures are allowable for applications in the semiconductor industry.
- It should be noted that the conductivity and the Na+ ion concentration are those in the water adhered on the sponge. COD is determined on pure water in which the PVAt sponge was crumpled and squeezed.
- The details of each measurement method and measured value will be described later in this specification.
- For the oxygen barrier film, poly(vinylidene chloride), nylon, poly(vinylacetate), poly(vinyl alcohol), aluminum foils, or aluminum deposited films can be preferably used. More preferably, films having an oxygen permeability of 10 cc/m2·atm· 24hrs at 20-25°C or lower are used. A laminated film consisting of two or more of these films having a high oxygen blocking property or a combination of the above-mentioned oxygen barrier film layered on a film such as a polyethylene, polyester, or polypropylene film are more preferred also for mechanical strength.
- As the outer package for double packaging, an oxygen barrier film as that used for the inner package can be used, but an oxygen permeating film can be used such as widely used materials, such as polyethylene, polypropylene, polyester, and nylon. The purpose of this outer package is that even if a PVAt sponge which is taken out from a clean room and contaminated on its outer package, contamination on the package can be removed just by removing the outer package before taken in the clean room again to thereby prevent contamination of the clean room.
- As the oxygen absorbent contained in the package made of a material with a high oxygen blocking property, substances which are chemically oxidized with ease can be used, for example, ascorbic acid, active metal powder, and sulfites, among which iron type substances are preferred in regard of their handling property, oxygen absorbing rate and oxygen absorbing capacity.
- In addition, it is more effective to use an oxygen absorbent in a form of fine powder to achieve a higher reactivity with oxygen. However, care should be taken not to bring the powder into contact with the porous material to be preserved. Generally, the oxygen absorbent fine powder is used with being wrapped in a material having smaller pores than a diameter of the oxygen absorbent and a gas permeability.
- Being stored in the above-mentioned manner, the PVAt sponge in the package can maintain for a long time the degree of cleanliness attained immediately after the cleaning with pure water.
- There are some simple methods to remove oxygen in a package such as a vacuum packaging method and a method of degassing the inside of the package followed by filling the inside with an inert gas such as nitrogen or argon gas. However, it is difficult to remove oxygen present inside the porous material completely by those methods. Therefere, it is preferred to use the present method together with the methods.
- To know whether oxygen exists in the package or not, it is effective to make the package to include a color-developing agent which reversibly changes its color depending upon the oxygen concentration. This facilitates it to know the oxygen concentration, so that more secure preservation of the products is achieved.
- Irradiating the packaged PVAt sponge with an electron beam or γ-ray sterilizes the PVAt sponge, so that mold growth can be prevented even when oxygen exists more or less. This means that any packaging material may be used satisfactorily as long as it can make a hermetic package and there is no need to use an oxygen barrier film. As a result, package and packaging procedure can be simplified.
- According to the present method, a PVAt sponge prepared by reacting PVA with formalin is cleaned thoroughly with water for general use to wash away reaction residues, unreacted substances, and additives. Then, the sponge is soaked in pure water having the aforesaid quality and subjected to mechanical stretching and compression. Subsequently, water contained in the sponge is squeezed out sufficiently and then the sponge is allowed to absorb another pure water, followed by the above procedures.
- Subsequently, the thus-cleaned PVAt sponge wet with pure water is covered as a whole with an oxygen barrier film and sealed completely. An oxygen absorbent is contained in the package together with the PVAt sponge. An oxygen detecting agent may also be contained. Alternatively, the whole PVAt sponge may be covered with a molded sheet article and then hermetically packaged as a whole with an oxygen barrier film.
- Upon oxygen present in the package being absorbed by the oxygen absorbent, the inner pressure in the package become sub-atmospheric, which causes the contained PVAt sponge to be deformed. If the deformation is kept for a long time, there may be a problem that the deformed part does not recover the original shape. This problem can be avoided by covering the whole PVAt sponge with a relatively hard, molded sheet article as described above.
- Further, contamination of environment where a sponge is used can be reduced further by double packaging a PvAt sponge packaged in an oxygen barrier film with a film, and discarding the outer package when the PVAT sponge is used.
- To avoid contamination by elements which are contained together with the PVAt sponge in the package such as the aforesaid oxygen absorbent and oxygen detecting agent, it is preferred not to bring these elements into direct contact with the PVAt sponge by providing, for example, a structure to fix these elements in a part of the molded sheet article.
- The present method can be applied not only to a porous material which hardens on drying but also to materials made of other polymers. For example, the present method can be applied to rubbery materials such as NBR and SBR and fibrous materials such as unwoven fabrics to prevent degradation of the materials themselves by oxidation or to preserve performances of agents added to the materials.
- As described above, cleaning a PVAt sponge and storing the sponge according to the present invention allows one to store the porous body in a wet state for a long period of time without contamination by fine particles, organic substances, ionsor the like and also without contamination by a moldproofing agent.
- Further, the present invention allows one to reduce or eliminate pre-cleaning which was conventionally practiced before using a PVAt sponge.
- In addition, the PVAt sponge is stored in an oxygen-free atmosphere for a long time and consequently mold growth and quality change of the porous body itself by oxidation can be prevented. Further, the present method can be applied widely to materials of which degradation by oxidation and quality change must be prevented, besides porous materials or wet materials.
- A method for each of the measurement items representing cleanliness will be explained below.
- Subject of measurement: a water sample is prepared by crumpling and squeezing 100cc of a sponge 100 times in 400 cc of distilled water and diluting it to 500 cc with tap water.
- Measurement method: the amount of potassium permanganate required to oxidize organic substances in the water sample is determined by coulometric titration and the amount is reduced to the equivalent amount of oxygen.
- Measurement instrument: portable, speedy type COD meter, HC-507, ex Central Kagaku Co.
- Subject of measurement: a water sample is prepared by squeezing a sponge which has been impregnated with a sufficient amount of DI water and allowed to stand for about 3 minutes.
Measurement method: electrodes are immersed in the sample and a conductivity is measured in an AC bipolar method.
Measurement instrument: compact conductivity meter, B-173 type, ex Horiba Seisakusho Co. - Subject of measurement: a water sample is prepared by crumpling and squeezing 10cc of a sponge 100 times in 800 cc of tap water and diluting it to 1000 cc with tap water.
Measurement method: a size of each particle in 10 cc of the sample is determined by voltage drop caused by cut-off of halogen light and the number of the particle is counted in a particle counter of a light cut-off type.
Measurement instrument: HIAC/ROYCO, MODEL4100 - Subject of measurement: a water sample is prepared by squeezing a sponge which has been impregnated with a sufficient amount of DI water and allowed to stand for about 3 miniutes.
Measurement method: the sample is dropped on a flat sensor of a sodium ion electrode.
Measurement instrument: compact Ion meter, CANDY C-122,ex Horiba Seisakusho Co. -
- Fig.1 is an illustrative view of the present storing method and Fig. 2 is an illustrative view of the structure of an oxygen barrier film used in the hermetic package.
- Fig.3 is an illustrative view of the sponge roller of Example 1 and Fig.4 is an illustrative view of washing with the brush roller of Fig.3.
- The present invention will be explained with reference to the following examples, but not limited to those Examples.
- A
sponge roller 1 made of poly(vinyl acetal) (PVAT) having an outer diameter cf 60mm, an inner diameter of 30 mm and a length of 254 mm was immersed in pure water having such water quality that its COD was 1 ppm, the conductivity at 25 °C was 0.06µ S/cm and the number of particles of 2.5µ or bigger was 0/ml. In the water, the sponge was forced to be stretched and compressed mechanically. Then, water contained in the sponge was squeezed out to remove the washing water. By repeating the above procedure with fresh pure water once again, the sponge was cleaned. After this cleaning, the wet sponge roller was placed in apackage 2 of 450 mm by 170 mm made of an oxygen barrier film as shown in Fig. 1, anoxygen absorbent 3 and an oxygen detecting agent 4 were introduced, and then the opening was heat sealed to thereby completely seal the package. - The oxygen barrier film used consists of 4 layers as shown in Fig.2. The film consists of a
top layer 5 of poly (vinylidene chloride), a second layer of nylon 6, a third layer ofpolyethylene 7 and a bottom layer of linear low density polyethylene 8, with the thickness of the layers being 5 µ m. 10µ m, 25µ m, and 60µ m, respectively. As the oxygen absorbent. Ageless FX-400, ex Mitsubishi Gas Co., was used . As the oxygen detecting agent, Ageless-eye KS, ex Mitsubishi Gas Co., was used. - This
sponge roller 1 is to be used for precision cleaning of aluminum disks or the like and, as shown in fig. 3, hasmany projections 9 on its surface. As shown in Fig.4, theseprojections 9 scrub and clean anobject 10 to be cleaned such as aluminum disks or the like in the presence of water or the like when thesponge roller 1 is rotated. - APVAt sponge roller was cleaned as in Example 1. After the cleaning, the wet sponge roller was placed in a package of 450 mm by 170 mm made of apolyechylene film and the opening was heat sealed to completely sael the package. This time, no oxygen absorbent and no oxygen detecting agent were introduced. The whole package was irradiated with an electron beam. Irradiation energy was 5 MeV and the dosage was 4kGy.
- A sponge roller of PVAt having an outer diameter of 60mn, an inner diameter of 30 mm and a length of 254 nm was wetted with the above-mentioned pure water, but no cleaning was applied. The roller was placed in a package of 450 mm by 170 mm made of an oxygen barrier film. The oxygen detecting agent was placed in the package, but no a oxygen absorbent was used and then the opening was heat sealed. The same kind of the oxygen barrier film as used in Example 1 was used.
- A sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was wetted with the above-mentioned pure water, but no cleaning was applied. The roller was placed in a package of 450 mm by 170 mm made of a polyethylene film. An oxygen absorbent and an oxygen detecting agent were also included and the opening was heat sealed. The same kinds of oxygen absorbent and the oxygen detecting agent as used in Example 1 were used.
- A sponge roller of PvAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was soaked in a mixture of 3,000 cc of a 0.3 wt% aqueous solution of sodium dehydroacetate and 3,000 cc of a 0.3 wt% aqueous solution of oxalic acid and a water content of the sponge roller was made equal to that in Example 1. Then, the sponge roller was placed in the same kind of a polyethylene film package as used in Comparative Example 2 together with an oxygen detecting agent, but without an oxygen absorbent, and the package was sealed completely. The same kind of an oxygen detecting agent as used in Example 1 was used.
- A sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was wetted with the above-mentioned pure water, but no cleaning was applied. The roller was placed in a package of 450 mm by 170 mm made of an oxygen barrier film. Air in the package was evacuated and then, nitrogen gas was introduced. The oxygen detecting agent was also placed in the package without an oxygen absorbent and package was sealed completely. The same kind of oxygen barrier film as used in Example 1 was used.
- A sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was cleaned as in Example 1. Then, after the cleaning, the wet sponge was placed in a package of 450 mm by 170 mm made of a polyethylene film together with the oxygen absorbent and the oxygen detecting agent and the package was heat sealed completely at its opening. The same kind of a polyethylene film as used in Comparative Example 2 was used.
- A sponge roller of PVAt having an outer diameter of 60mm, an inner diameter of 30 mm and a length of 254 mm was cleaned as in Example 1. Then, after the cleaning, the wet sponge was placed in a package of 450 mm by 170 mm made of a polyethylene film together with the oxygen detecting agent, but without an oxygen absorbent, and the package was heat sealed completely at its opening. The same kind of a polyethylene film as used in Comparative Example 2 was used.
- The PVAt sponge rollers treated as described above were stored in a thermostatic room kept at 23 °C and change in appearance was observed for 200 - days. Appearances of the porous rollers. i.e., the degree of mold growth was as shown in the following Table 1.
Table 1 Degree of mold growth days 10 days 30 days 60 days 100 days 200 days Example 1 - - - - - Example 2 - - - - - Comparative example 1 - + ++ +++ +++ Comparative example 2 - - + ++ +++ Comparative example 3 - - - - - Comparative example 4 - - - + ++ Comparative example 5 - - - - + Comparative example 6 - - - + ++ - :Mold growth was not detected. + : At least 1 colony of mold was detected. ++ :At least 3 colonies of mold were detected. + + + :At least 10 colonies of mold were detected. - As shown in Table 1, mold growth was prevented for at least 200 days according to the present PVAt sponge roller, the present preparing method and the present storing method in Example 1.
- Also in Example 2, the irradiation of an electron beam on the packaged sponge roller prevented mold growth for at least 200 days as in Example 1. This is achieved because the irradiation with an electron beam sterilizes the sponge roller to thereby prevent mold growth even when there is a little oxygen. This means that any package which can be sealed may be used satisfactorily and it is unnecessary to use an oxygen barrier film. Further, a package and a packaging process can be simpler.
- Comparative Example 3 in Table 1 shows, a conventional method where a moldproofing agent was used. Although mold did not grow, the purpose of the present invention could not be achieved.
- In contrast with this, in the other Comparative Examples, no moldproofing agent was used. Farther, in Comparative Examples 1,2 and 4, cleaning with pure water was not applied. In comparative Example 1, because no oxygen absorbent was included, mold grows due to residual oxygen in the packages. In Comparative Example 2, the film of the package does not have an oxygen blocking property. Accordingly, when the amount of oxygen which penetrated the film exceeded the capacity of the oxygen absorbent, mold grew. In Comparative Example 4, air in the package was replaced with nitrogen gas first and the oxygen barrier film was used. Mold could grow due to oxygen which penetrated the film gradually and no oxygen absorbent was included, though mold grew slower than in Comparative Examples 1 and 2.
- In Comparative Examples 5 and 6, cleaning with pure water was carried out. In the both Examples, a polyethylene film was used but no oxygen barrier film was used. In Comparative Example 5, an oxygen absorbent was included, and accordingly the result is better than in the other Comparative Examples, but not as good as in the Examples. In Comparative Example 6, the result is worse than that of Comparative Example 5 because no oxygen absorbent was included.
- Thus, to keep a PVAt sponge in a wet state without getting moldy, it is necessary to make the inside of the package for storing to be oxygen-free orat an oxygen concentration which is almost oxygen-free. For that purpose, a PVAt sponge should be hermetically packaged together with an oxygen absorbent with an oxygen barrier film according to the present invention.
- As shown in the Examples, to store a PVAt sponge in a wet state, mold growth can be restrained for an prolonged period of time by cleaning the PVAt sponge with pure water and keeping it in an oxygen-free or almost oxygen-free atmosphere.
- Next the package of the roller which was stored for 200 days as discuted above was opened and the roller was subjected to the determinated of conductivity in accordance with the method mentioned above. The roller was subjected to the pre-cleaning and the conductivity at each pre-cleaning was determined. The result are as shown in Table 2.
- In the Examples, the amount of the eluted components come within the allowable range in a short period of cleaning. In comparative Examples 1, 2 and 4, a longer cleaning period is necessary because cleaning with pure water was not conducted. In Comparative Example 3, the conductivity is higher due to the eluted moldproofing agent.
- In Comparative Examples 5 and 6, cleaning with pure water was conducted and accordingly the results are comparable to those of Examples 1 and 2.
Table 2 Conductivity, µ S/ cm Pre-cleaning time, hour 0 1 2 3 4 Example 0.5 0.1 0.06 0.06 0.06 Comparative example 1 5.0 1.0 0.5 0.1 0.1 Comparative example 2 5.0 1.0 0.5 0.1 0.1 Comparative example 3 400 50 20 5 1. Comparative example 4 5.0 1.0 0.5 0.1 0.1 - Table 3 shows whether oxygen was detected or not by the oxygen detecting agents contained in the packages. In Table 3, "none" means that the oxygen concentration was 0.1% or smaller.
- In Example 1, the inside of the package was kept oxygen free for a long time. In contrast with it, in the Comparative Examples, the oxygen concentration could be maintained low for a short time in some cases, but not for a long time.
Table 3 Presence of oxygen in the package days 10 days 30 days 60 days 100 days 200 days Example 1 No No No No No Example 2 Yes Yes Yes Yes Yes Comparative example 1 Yes Yes Yes Yes Yes Comparative example 2 No Yes Yes Yes Yes Comparative example 3 Yes Yes Yes Yes Yes Comparative example 4 No No Yes Yes Yes Comparative example 5 No Yes Yes Yes Yes Comparative example 8 Yes Yes Yes Yes Yes - As shown in Example 1, to store a PVAt sponge in a wet state, mold growth can be restrained for a long time by cleaning the PVAt sponge with pure water and keeping it in an oxygen-free or almost oxygen-free atmosphere.
- The present invention allows one to keep porous bodies oxygen-free for a long time and , therefore, can prevent change in quality of porous bodies by oxidation in addition to a moldproofing effect. Further, the present storing method can be used to store not only porous materials or wet materials but also those which should be protected from degradation by oxidation or quality change.
- In Example 2, mold growth was prevented even in the presence of oxygen as far as the package was hermetic, because the sponge was sterilized by irradiation with an electron beam.
- The present storing method can greatly reduce the amount of eluted substances and dust from a PVAt sponge; can shorten or eliminate pretreatment such as washing before used; maintains the moldproofing effect for a long time even when storing the PVAt sponge in a wet state; and prevents degradation by oxidation or deterioration because the porous material is kept oxygen free. Therefore, the present method is extremely useful.
Claims (19)
- A porous poly(vinyl acetal) resin body having a high degree of cleanliness, characterized in that the porous body shows a COD of 5 ppm or less and a concentration of sodium ions of 1 ppm or less.
- A porous poly (vinyl acetal) resin body having a high degree of cleanliness, characterized in that the porous body shows a conductivity of less than 5 µ S/cm, COD of 5ppm or smaller, and the number of particles having a size of 2.5 µm or larger is at most 50,000/cc of the porous body.
- A method of preparing a porous poly (vinyl acetal) resin body having a high degree of cleanliness according to claim 1 or claim 2, characterized in that the method comprises a step of cleaning the body with pure water from which particles, ions and organic substances dissolved or floating in the water have been removed.
- The method of preparing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 3, wherein the pure water used for the cleaning has a conductivity of 0.1 µ S/cm or lower and a COD of 1 ppm or less.
- The method of preparing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 3, wherein the step of cleaning with pure water is carried out in an environment where a higher degree of cleanliness than Class 100 specified in the Federal Standards 209D is maintained.
- A method of storing a porous poly(vinyl acetal) resin body prepared with a high degree of cleanliness according to claim 1 or claim 2, characterized in that the method comprises a step of hermetically packaging the body with an oxygen barrier film.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 6, wherein an oxygen absorbent is contained in the hermetic package made of the oxygen barrier film.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 6, wherein the oxygen barrier film has an oxygen permeability of 200 cc/m2. atm·24 hrs or smaller.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 6, wherein an oxygen detecting agent is contained in the hermetic package.
- A method of storing a porous poly (vinyl acetal) resin body having a high degree of cleanliness according to claim 1 or claim 2, characterized in that the method comprises steps of hermetically packaging the porous poly(vinyl acetal) resin body and irradiating the hermetic package with an electron beam or γ-ray.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 10, wherein an irradiation dosage of the electron beam or γ-ray is 10 kGy or smaller.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 10, wherein an oxygen barrier film is used for a hermetic package and an oxygen absorbent is contained in the hermetic package.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 12, wherein the oxygen barrier film has an oxygen permeability of 200 cc/m2· atm · 24 hrs or smaller.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 6, wherein the step of hermetically packaging is carried out in an environment where a higher degree of cleanliness than Class 100 specified in the Federal standards 209D is maintained.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 6, wherein the porous poly (vinyl acetal) resin body is covered by a molded sheet article before hermetically packaging the body with a high degree of cleanliness.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 6, wherein the hermetic package is further covered and sealed with a film material to provide double packaging.
- The porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 1, wherein the porous poly(vinyl acetal) resin body is a sponge roller used for cleaning.
- The method of preparing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 3, wherein the porous poly(vinyl acetal) resin body is a sponge roller used for cleaning.
- The method of storing a porous poly(vinyl acetal) resin body having a high degree of cleanliness according to claim 6, wherein the porous poly(vinyl acetal) resin body is a sponge roller used for cleaning.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP1997/004249 WO1999027003A1 (en) | 1997-11-21 | 1997-11-21 | Highly clean porous polyvinyl acetal resin, method for preparing the same, and method for storing the same |
Publications (3)
Publication Number | Publication Date |
---|---|
EP1035157A1 EP1035157A1 (en) | 2000-09-13 |
EP1035157A4 EP1035157A4 (en) | 2001-02-07 |
EP1035157B1 true EP1035157B1 (en) | 2006-03-08 |
Family
ID=14181510
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97913421A Expired - Lifetime EP1035157B1 (en) | 1997-11-21 | 1997-11-21 | Highly clean porous polyvinyl acetal resin, method for preparing the same, and method for storing the same |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1035157B1 (en) |
AU (1) | AU5066398A (en) |
DE (1) | DE69735412T2 (en) |
WO (1) | WO1999027003A1 (en) |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS596974A (en) * | 1982-07-05 | 1984-01-14 | カネボウ株式会社 | Washing method |
US5340407A (en) * | 1988-02-08 | 1994-08-23 | Petroferm Inc. | Process of removing soldering flux and/or adhesive tape residue from a substrate |
JPH06166713A (en) * | 1992-08-19 | 1994-06-14 | Daiwa Kagaku Kogyo Kk | Production of polyvinyl acetal-based porous material having antimicrobial and mildew-proofing property |
EP0937509A4 (en) * | 1996-11-08 | 2005-01-19 | Aion Co Ltd | Sponge roller for cleaning |
JP3344556B2 (en) * | 1997-11-20 | 2002-11-11 | アイオン株式会社 | High cleanliness polyvinyl acetal resin porous body and its storage method |
JP3806857B2 (en) * | 1998-11-26 | 2006-08-09 | アイオン株式会社 | Polyvinyl acetal sponge and method for producing the polyvinyl acetal sponge |
-
1997
- 1997-11-21 AU AU50663/98A patent/AU5066398A/en not_active Abandoned
- 1997-11-21 WO PCT/JP1997/004249 patent/WO1999027003A1/en active IP Right Grant
- 1997-11-21 DE DE69735412T patent/DE69735412T2/en not_active Expired - Lifetime
- 1997-11-21 EP EP97913421A patent/EP1035157B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DE69735412D1 (en) | 2006-05-04 |
AU5066398A (en) | 1999-06-15 |
DE69735412T2 (en) | 2006-08-10 |
EP1035157A1 (en) | 2000-09-13 |
EP1035157A4 (en) | 2001-02-07 |
WO1999027003A1 (en) | 1999-06-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7337592B2 (en) | Porous poly(vinyl acetal) resin body having a high degree of cleanliness, a process of preparing the same, and a method of storing the same | |
US6176067B1 (en) | Method for packaging sponge or porous polymeric products | |
KR20200023607A (en) | Steam Sterilized Catheter Assembly | |
FR2756259A1 (en) | Manufacturing dry sterile packaging for sterile articles | |
EP1543842A1 (en) | Method of sterilizing a biocompatible material | |
EP1035157B1 (en) | Highly clean porous polyvinyl acetal resin, method for preparing the same, and method for storing the same | |
JP3115729U (en) | Peroxide storage | |
JP3344556B2 (en) | High cleanliness polyvinyl acetal resin porous body and its storage method | |
JPH09316229A (en) | High-cleanliness polyvinyl formal resin porous material | |
WO2017002277A1 (en) | Sterilization sheet pack and method for producing sterilization sheet | |
JP2000086805A (en) | Method of storing polyvinyl formal resin porous material and storage structure | |
US20050287032A1 (en) | Anti-bacterial protection to improve performance of post CMP clean brush | |
JP2008173287A (en) | Radiation sterilization method for hollow fiber membrane type blood purifier and hollow fiber membrane type blood purifier | |
JP2901669B2 (en) | Manufacturing method of radiation sterilized medical device | |
JPS6024945A (en) | Laminated film suitable for boiling sterilization | |
JP3201842B2 (en) | Manufacturing method of potatoes packed in pouches | |
KR930005885B1 (en) | Container for citrus fruit juice | |
JPH0662378B2 (en) | Ozone-adsorbing microbial control material and microbial control method | |
JP4061448B2 (en) | How to store goods | |
JP2005095271A (en) | Aseptic packaging method for hollow thread type blood treatment device | |
CN117481192A (en) | Food preservative and preservation method | |
JP2001169722A (en) | Package for retaining vegetable and fruit freshness | |
JPH0432699B2 (en) | ||
JPH0215251B2 (en) | ||
JPS5819259A (en) | Pasturization of medical tool |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20000621 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE GB IE |
|
A4 | Supplementary search report drawn up and despatched |
Effective date: 20001227 |
|
AK | Designated contracting states |
Kind code of ref document: A4 Designated state(s): DE GB IE |
|
RIC1 | Information provided on ipc code assigned before grant |
Free format text: 7C 08J 9/00 A, 7B 08B 1/00 B, 7A 47L 25/00 B, 7C 08F 8/28 B |
|
17Q | First examination report despatched |
Effective date: 20030502 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE GB IE |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REF | Corresponds to: |
Ref document number: 69735412 Country of ref document: DE Date of ref document: 20060504 Kind code of ref document: P |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20061211 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20081013 Year of fee payment: 12 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20091121 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20091121 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IE Payment date: 20161111 Year of fee payment: 20 Ref country code: DE Payment date: 20161118 Year of fee payment: 20 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R071 Ref document number: 69735412 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: MK9A |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION Effective date: 20171121 |