[go: up one dir, main page]

WO2013019044A2 - Sterilant container and system for supplying fixed amount of sterilant of sterilizer using same - Google Patents

Sterilant container and system for supplying fixed amount of sterilant of sterilizer using same Download PDF

Info

Publication number
WO2013019044A2
WO2013019044A2 PCT/KR2012/006050 KR2012006050W WO2013019044A2 WO 2013019044 A2 WO2013019044 A2 WO 2013019044A2 KR 2012006050 W KR2012006050 W KR 2012006050W WO 2013019044 A2 WO2013019044 A2 WO 2013019044A2
Authority
WO
WIPO (PCT)
Prior art keywords
sterilant
container
outlet
sterilizer
valve
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.)
Ceased
Application number
PCT/KR2012/006050
Other languages
French (fr)
Korean (ko)
Other versions
WO2013019044A3 (en
Inventor
์ด์ƒ์ผ
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
LOWTEM CO Ltd
Original Assignee
LOWTEM CO Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by LOWTEM CO Ltd filed Critical LOWTEM CO Ltd
Publication of WO2013019044A2 publication Critical patent/WO2013019044A2/en
Publication of WO2013019044A3 publication Critical patent/WO2013019044A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/16Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
    • A61L2/18Liquid substances or solutions comprising solids or dissolved gases
    • A61L2/186Peroxide solutions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS 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
    • B65D47/00Closures with filling and discharging, or with discharging, devices
    • B65D47/04Closures with discharging devices other than pumps
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/24Apparatus using programmed or automatic operation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/26Accessories or devices or components used for biocidal treatment
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2202/00Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
    • A61L2202/10Apparatus features
    • A61L2202/12Apparatus for isolating biocidal substances from the environment
    • A61L2202/122Chambers for sterilisation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2202/00Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
    • A61L2202/10Apparatus features
    • A61L2202/15Biocide distribution means, e.g. nozzles, pumps, manifolds, fans, baffles, sprayers

Definitions

  • the present invention relates to a sterilant container and a sterilant quantitative supply system of the sterilizer using the same, and more particularly, to provide convenience and safety in transportation, storage and handling of the sterilant container, and to enable reuse of the sterilant container. It relates to a sterilant container and a sterilant quantitative supply system of the sterilizer using the same to reduce the cost.
  • a sterilant supply system has been used, such as a method of subdividing and using a fixed amount, and a method of subdividing and using a fixed amount by storing in an internal storage space.
  • the bottle type sterilant supply system once the bottle is installed once it can not be removed until it is used, since the inlet is destroyed after installation, there is a problem that the inconvenience and risk of removing the bottle, it is impossible to reuse .
  • additional systems are needed to collect and remove the remaining sterilizers, which increases manufacturing costs and poses risks.
  • the sterilant supply system for storing the sterilant in a separate internal storage space is very susceptible to contamination in the case of hydrogen peroxide, the concentration may be lowered, it is difficult to supply by subdividing with a very precise quantitative, remaining or shortage of sterilant In this case, it was difficult to supply a fixed quantity.
  • the present invention is easy to transport and storage because the sterilant container has an overpressure preventing function, so that the sterilant container can be in any position such as upside down, and is easy to transport and store. In addition to being open, it should be sealed when it is detached to promote convenience and safety.
  • the configuration for supplying the sterilant from the sterilant container is simple and the supply of the sterilant is made to be stable to lower the manufacturing cost and to increase the reliability of the quantitative supply.
  • the outlet for the injection and discharge of the sterilant is A container provided;
  • An automatic sealing valve installed at the outlet to maintain the outlet in a closed state and opening the outlet when mounted in the sterilant supply system;
  • a sterilant container provided in the container and including an overpressure preventing unit for preventing overpressure of the container.
  • the container may be provided with a valve interference prevention groove on one side such that the automatic sealing valve is located inside, and the overpressure prevention unit may be provided on the opposite side of the outlet side and inside the valve interference prevention groove, respectively.
  • the container in which the sterilant is stored, and installed in the outlet of the container to maintain the outlet is closed and the outlet is opened by pressing
  • a sterilant container having an automatic sealing valve to enable A sterilant container mounted to be connected to the automatic sealing valve, and a mounting part for opening the automatic sealing valve by pressing the automatic sealing valve to open the outlet;
  • a flow rate control unit installed in a sterilant supply line providing a path for supplying a sterilant discharged from the outlet to a sterilization chamber, and controlling a flow rate of the sterilant;
  • An on / off valve installed in the sterilant supply line to open and close the supply of the sterilant;
  • the sterilant container, the valve interference prevention groove is formed so that the automatic sealing valve is located on one side of the container, the overpressure preventing unit is provided in the container to prevent the overpressure of the container, the overpressure preventing unit It may be provided on the opposite side of the outlet side and the inside of the valve interference prevention groove, respectively.
  • Branch line branching from the front end of the metering cylinder in the sterilant supply line;
  • a vent valve installed at the branch line;
  • And installed at the rear end of the vent valve in the branch line, and may further include a filter for blocking microorganisms or foreign matter infiltrate into the branch line.
  • the mounting unit may further include a container chamber installed in the inner space and provided with a door for opening and closing the inner space.
  • the sterilant container and the sterilant quantitative supply system of the sterilizer using the same provides convenience and safety in the transportation, storage and handling of the sterilant container, reducing the cost by enabling the reuse of the sterilant container It does not require an additional removal system to remove sterilant containers with residual or exhausted sterilant, which not only simplifies the construction of the equipment, but also lowers the manufacturing cost, and allows a single installation of the sterilant container several times. Allow the supply of sterile agents.
  • FIG. 1 is a block diagram showing a sterilant quantitative supply system of the sterilizer according to an embodiment of the present invention
  • FIG. 2 and 3 is a perspective view showing a sterilant container according to an embodiment of the present invention
  • Figure 4 is a perspective view showing a container chamber of the sterilant container according to an embodiment of the present invention.
  • FIG. 1 is a block diagram showing a sterilant quantitative supply system of the sterilizer according to an embodiment of the present invention.
  • the sterilant quantitative supply system 100 of the sterilizer is a sterilant container 110, the mounting portion 120, the flow control unit 130, opening and closing
  • the valves 140, 170, and 190 may include a metering cylinder 150 and a vaporizer 180.
  • the sterilant container 110 according to the present invention will be described together in the sterilant quantitative supply system 100 of the sterilizer.
  • the sterilant container 110 may include a container 111 and an automatic sealing valve 112, and further include an overpressure preventing unit 113.
  • the container 111 is a sterilant, for example, hydrogen peroxide is stored therein, an outlet (not shown) for injecting and discharging the sterilant is provided, and is made of a material to withstand the pressure of the sterilant, and as shown in the embodiment
  • the container can of course have various shapes.
  • the automatic sealing valve 112 is installed at the outlet to maintain the outlet of the container 111 in a closed state, for example to open the outlet by pressing action, the mounting portion 120 of the sterilant supply system 100 Make sure the outlet is open when mounted on On the other hand, the automatic sealing valve 112 seals the outlet of the container 111 by closing the flow path by the inner sealing member by the elastic force of the spring, the sealing member by the pin of the mounting portion 120 when mounted on the mounting portion 120 Is pressed to open the outlet of the container 111 by opening the flow path while pressing the spring.
  • the overpressure preventing unit 113 is provided in the container 111 and prevents overpressure of the container 111.
  • the blocking member is compressed by the spring 111.
  • the blocking member By opening the outlet of the) to prevent the container 111 from being above a predetermined pressure, and when the pressure in the container 111 is less than the predetermined pressure, the blocking member is configured to seal the outlet of the container 111 by expansion of the spring.
  • the container 111 is installed inside the container 111, and when the pressure in the container 111 is greater than or equal to a predetermined pressure, the blocking member compresses the spring to move inside the sealed space provided in the container 111 to store the container ( When the volume in the container 111 is increased, and the pressure in the container 111 is less than the predetermined pressure, the blocking member is moved out of the closed space by a spring so that the volume in the container 111 decreases.
  • the lock may be configured.
  • the container 111 has a valve interference preventing groove 114 formed at one side such that the automatic sealing valve 112 is located inside, and the overpressure preventing unit 113 has an opposite side of the outlet side and an inner side of the valve interference preventing groove 114.
  • Each may be provided in plurality.
  • Mounting unit 120 is equipped with a sterilant container 110 to be connected to the automatic sealing valve 112, it may be screwed to the inlet of the automatic sealing valve 112, for example, the automatic sealing valve 112 by a pin By pressing to open the outlet of the container 111 is opened to enable the discharge of the sterilant.
  • Flow control unit 130 is installed in the sterilant supply line 210 to provide a path for supplying the sterilant discharged from the outlet to the sterilization chamber 10, and adjusts the flow rate of the sterilant.
  • the flow control unit 130 may be made of, for example, a flow control valve, and the valve may be made of a manual valve or a control valve that operates according to a control signal.
  • the sterilization chamber 10 forms a part of the sterilizer, and provides a closed space for sterilization objects located inside to be sterilized by the sterilizing agent.
  • Opening / closing valves 140, 170, and 190 are installed in the sterilant supply line 210 to open and close the supply of the sterilant, and may be made of a control valve operating in accordance with a control signal, made of a single, or flow cylinder 150 as in this embodiment
  • a control signal made of a single, or flow cylinder 150 as in this embodiment
  • the metering cylinder 150 is to be supplied in a quantitative manner through the sterilant supply line 210 through the quantitative confirmation sensor 160 for measuring the flow rate of the sterilant passing through the flow control unit 130, for example shear
  • the vacuum supplied from the outside is filled inside, and the sterilizing agent is introduced from the sterilant container 110 by the vacuum, and the sterilizing agent filled inside is It is to be supplied to the vaporizer 180 to form a low pressure.
  • control unit (not shown) provided in the quantitative cylinder 150 or separate from the quantitative cylinder 150 calculates the flow rate of the sterilant detected through the quantitative confirmation sensor 160 so that the sterilant is supplied in a quantitative manner.
  • the operation of the 150 may be controlled, and further, the open / close valves 140 and 170 respectively installed at the front and rear ends of the metering cylinder 150 may be controlled to supply the metered amount of the sterilant by the metering cylinder 150, respectively. .
  • the vaporizer 180 vaporizes the sterilant passed through the metering cylinder 150 and supplies it to the sterilization chamber 10 so that the sterilizing agent is supplied to the sterilization chamber 10 in a vaporized state so that the sterilization operation is smoothly performed. Meanwhile, the vaporizer 180 may allow the sterilizing agent to be vaporized by providing heat or lowering the pressure.
  • Branch line 220 may be branched to the sterilant supply line 210, this branch line 220 is provided to branch from the front end of the metering cylinder 150 in the sterilant supply line 210, vent valve ( vent valve 230 and filter 240 are installed.
  • the vent valve 230 may be formed of, for example, a control valve operated by a control signal, and may be opened to allow the sterilant to be discharged through the branch line 220.
  • the filter 240 is installed at the rear end of the vent valve 230 in the branch line 220 to block the invasion of microorganisms or foreign substances into the branch line 220, for example, a bacterial filter may be used.
  • the mounting part 120 may be installed inside the container chamber 250, and the container chamber 250 may have an inner space 251 for mounting the mounting part 120.
  • a door 252 for opening and closing the space 251 is provided by a hinge coupling, and a locking member 253 is provided on one side of the door 252 and the side facing the door 252 for locking and unlocking the door 252. do.
  • the sterilant container 110 by the overpressure prevention unit 113, even if installed in any position, the nature of the sterilant such as hydrogen peroxide Even if the pressure increases due to decomposition, it is easy to transport, store, handle, etc., and the safety can be improved.
  • the sterilant container 110 is to be opened only when mounted to the mounting portion 120 by the automatic sealing valve 112, and to be sealed when detached to the mounting portion 120 to separate the device in use or removed after use Is not necessary.
  • the sterilant metering supply system 100 forms a vacuum in the metering cylinder 150, seals the metering cylinder 150 using the opening / closing valves 140 and 170 before and after the metering cylinder 150, and then the metering cylinder ( 150) by opening the opening and closing valve 140 of the front end to fill the desired amount of the sterilizing agent in the cylinder 150.
  • the metering cylinder ( 150) by opening the opening and closing valve 140 of the front end to fill the desired amount of the sterilizing agent in the cylinder 150.
  • the on / off valve 170 at the rear end of the metering cylinder 150 is opened so that the sterilant in the metering cylinder 150 is supplied to the vaporizer 180 having a low pressure.
  • the outlet for the injection and discharge of the sterilant is A container provided;
  • An automatic sealing valve installed at the outlet to maintain the outlet in a closed state and opening the outlet when mounted in the sterilant supply system;
  • a sterilant container provided in the container and including an overpressure preventing unit for preventing overpressure of the container.
  • the container may be provided with a valve interference prevention groove on one side such that the automatic sealing valve is located inside, and the overpressure prevention unit may be provided on the opposite side of the outlet side and inside the valve interference prevention groove, respectively.
  • the container in which the sterilant is stored, and installed in the outlet of the container to maintain the outlet is closed and the outlet is opened by pressing
  • a sterilant container having an automatic sealing valve to enable A sterilant container mounted to be connected to the automatic sealing valve, and a mounting part for opening the automatic sealing valve by pressing the automatic sealing valve to open the outlet;
  • a flow rate control unit installed in a sterilant supply line providing a path for supplying a sterilant discharged from the outlet to a sterilization chamber, and controlling a flow rate of the sterilant;
  • An on / off valve installed in the sterilant supply line to open and close the supply of the sterilant;
  • the sterilant container, the valve interference prevention groove is formed so that the automatic sealing valve is located on one side of the container, the overpressure preventing unit is provided in the container to prevent the overpressure of the container, the overpressure preventing unit It may be provided on the opposite side of the outlet side and the inside of the valve interference prevention groove, respectively.
  • Branch line branching from the front end of the metering cylinder in the sterilant supply line;
  • a vent valve installed at the branch line;
  • And installed at the rear end of the vent valve in the branch line, and may further include a filter for blocking microorganisms or foreign matter infiltrate into the branch line.
  • the mounting unit may further include a container chamber installed in the inner space and provided with a door for opening and closing the inner space.
  • the sterilant quantitative supply system according to the present invention can be used for sterilization devices and the like.
  • sterilization chamber 110 sterilant container

Landscapes

  • Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)

Abstract

The present invention provides a sterilant container mounted on a sterilant supply system of a sterilizer, and the sterilant container comprises: a container in which a sterilant is stored, and which has an exit for injecting and discharging said sterilant; an automatic sealing valve which is installed at said exit such that said exit is maintained in a sealed state, and allows said exit to be opened when being mounted on said sterilant supply system; and an overpressure prevention unit which is provided in said container, and prevents overpressure of said container.

Description

๋ฉธ๊ท ์ œ ์šฉ๊ธฐ ๋ฐ ์ด๋ฅผ ์ด์šฉํ•œ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œSterilizer container and sterilizer quantitative supply system using the sterilizer

๋ณธ ๋ฐœ๋ช…์€ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ ๋ฐ ์ด๋ฅผ ์ด์šฉํ•œ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ๊ด€ํ•œ ๊ฒƒ์œผ๋กœ์„œ, ๋ณด๋‹ค ์ƒ์„ธํ•˜๊ฒŒ๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์˜ ์šด์†ก, ๋ณด๊ด€ ๋ฐ ์ทจ๊ธ‰์— ์žˆ์–ด์„œ ํŽธ๋ฆฌํ•จ๊ณผ ์•ˆ์ „ํ•จ์„ ์ œ๊ณตํ•˜๊ณ , ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์˜ ์žฌ์‚ฌ์šฉ์„ ๊ฐ€๋Šฅํ•˜๋„๋ก ํ•˜์—ฌ ๋น„์šฉ์„ ์ ˆ๊ฐํ•˜๋„๋ก ํ•˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ ๋ฐ ์ด๋ฅผ ์ด์šฉํ•œ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ๊ด€ํ•œ ๊ฒƒ์ด๋‹ค.The present invention relates to a sterilant container and a sterilant quantitative supply system of the sterilizer using the same, and more particularly, to provide convenience and safety in transportation, storage and handling of the sterilant container, and to enable reuse of the sterilant container. It relates to a sterilant container and a sterilant quantitative supply system of the sterilizer using the same to reduce the cost.

์ผ๋ฐ˜์ ์œผ๋กœ, ํ™”ํ•™ ์šฉ์•ก ๋“ฑ์„ ๋ฉธ๊ท ์ œ๋กœ ์‚ฌ์šฉํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๊ฒฝ์šฐ ๋ฉธ๊ท ์ œ์˜ ์–‘์„ ์ผ์ •ํ•˜๊ฒŒ ๊ณต๊ธ‰ํ•ด ์ฃผ๋Š” ์‹œ์Šคํ…œ์ด ํ•„์š”ํ•˜๋‹ค.In general, in the case of a sterilizer using a chemical solution or the like as a sterilizer, a system for supplying a constant amount of sterilant is required.

์ข…๋ž˜์— ๊ณผ์‚ฐํ™”์ˆ˜์†Œ๋ฅผ ๋ฉธ๊ท ์ œ๋กœ ์‚ฌ์šฉํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๊ฒฝ์šฐ, ํ•œ๋ฒˆ์— ํ•˜๋‚˜์˜ ์•ฐํ”Œ(ampoule)์„ ๊ณต๊ธ‰ํ•˜์—ฌ ์‚ฌ์šฉํ•˜๋Š” ๋ฐฉ์‹๊ณผ, ์—ฌ๋Ÿฌ ์•ฐํ”Œ์„ ์นด์…‹ํŠธ ํƒ€์ž…(cassette type)์œผ๋กœ ๋ชจ์•„์„œ ์‚ฌ์šฉํ•˜๋Š” ๋ฐฉ์‹๊ณผ, ๋ณดํ‹€ ํƒ€์ž…(bottle type)์œผ๋กœ ์ •๋Ÿ‰์„ ์†Œ๋ถ„ํ•˜์—ฌ ์‚ฌ์šฉํ•˜๋Š” ๋ฐฉ์‹๊ณผ, ๋‚ด๋ถ€ ์ €์žฅ๊ณต๊ฐ„์— ์ €์žฅํ•˜์—ฌ ์ •๋Ÿ‰์„ ์†Œ๋ถ„ํ•˜์—ฌ ์‚ฌ์šฉํ•˜๋Š” ๋ฐฉ์‹ ๋“ฑ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์ด ์ด์šฉ๋˜๊ณ  ์žˆ๋‹ค.Conventionally, in the case of a sterilizer using hydrogen peroxide as a sterilizing agent, one ampoule is supplied at a time and used, and a plurality of ampoules are collected in a cassette type and a bottle type. A sterilant supply system has been used, such as a method of subdividing and using a fixed amount, and a method of subdividing and using a fixed amount by storing in an internal storage space.

๊ทธ๋Ÿฌ๋‚˜, ์ด๋Ÿฌํ•œ ๋ฐฉ์‹์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์—์„œ ํ•˜๋‚˜์˜ ์•ฐํ”Œ์„ ์‚ฌ์šฉํ•˜๋Š” ๊ฒฝ์šฐ, ๋ช‡ ํšŒ ์‚ฌ์šฉํ•˜์ง€ ๋ชปํ•˜๋ฏ€๋กœ ์‚ฌ์šฉ์ž๊ฐ€ ๋นˆ๋ฒˆํ•˜๊ฒŒ ๊ต์ฒดํ•ด ์ฃผ์–ด์•ผ ํ•˜๋Š” ๋ถˆํŽธํ•จ์„ ๊ฐ€์ง€๊ณ  ์žˆ์—ˆ๋‹ค. ๋˜ํ•œ, ์•ฐํ”Œ์„ ๋ฉธ๊ท  ๊ณต์ •์—์„œ ํ„ฐํŠธ๋ ค์•ผ ํ•˜๊ณ , ์ข…๋ฃŒ ํ›„ ์œ ๋…ํ•œ ํ™”ํ•™ ๋ฌผ์งˆ์ด ๋ฌป์–ด ์žˆ๊ธฐ ๋•Œ๋ฌธ์— ์‚ฌ์šฉ์ž๊ฐ€ ์ง์ ‘ ๋งŒ์งˆ ์ˆ˜ ์—†๊ณ , ์ด๋กœ ์ธํ•ด ์ด๋ฅผ ๋”ฐ๋กœ ๋ชจ์•„ ์ฒ˜๋ฆฌํ•˜๋Š” ์‹œ์Šคํ…œ์ด ์žˆ์–ด์•ผ ํ•˜๋ฏ€๋กœ ์ œ์กฐ๋น„์šฉ์ด ๋†’๊ณ , ์ฒ˜๋ฆฌ์— ์žˆ์–ด ๋ถˆํŽธํ•จ๊ณผ ์œ„ํ—˜์ด ์žˆ๋‹ค๋Š” ๋ฌธ์ œ์ ์„ ๊ฐ€์ง€๊ณ  ์žˆ์—ˆ๋‹ค.However, in the case of using a single ampoule in this type of sterilant supply system, it was inconvenient to be replaced frequently by the user because it cannot be used several times. In addition, the ampoule must be exploded in the sterilization process, and since the toxic chemicals are terminated after the end, the user cannot touch it directly, which requires a system to collect and process it separately. There was a problem of danger.

๋˜ํ•œ, ๋ณดํ‹€ ํƒ€์ž… ๋ฐฉ์‹์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์€, ๋ณดํ‹€์„ ํ•œ๋ฒˆ ์žฅ์ฐฉํ•˜๋ฉด ๋‹ค ์‚ฌ์šฉํ•  ๋•Œ๊นŒ์ง€ ์ œ๊ฑฐํ•˜์ง€ ๋ชปํ•˜๋ฉฐ, ์žฅ์ฐฉ ํ›„ ์ž…๊ตฌ๊ฐ€ ํŒŒ๊ดด๋˜๋ฏ€๋กœ ๋ณดํ‹€์˜ ์ œ๊ฑฐ์‹œ ๋ถˆํŽธํ•จ๊ณผ ์œ„ํ—˜์„ ์ดˆ๋ž˜ํ•˜๊ณ , ์žฌ์‚ฌ์šฉ์ด ๋ถˆ๊ฐ€๋Šฅํ•˜๋‹ค๋Š” ๋ฌธ์ œ์ ์ด ์žˆ์—ˆ๋‹ค. ๋”์šฑ์ด ๋‚จ์€ ๋ฉธ๊ท ์ œ๋ฅผ ๋”ฐ๋กœ ๋ชจ์•„์„œ ์ œ๊ฑฐํ•ด ์ฃผ๋Š” ์‹œ์Šคํ…œ์ด ์ถ”๊ฐ€๋กœ ํ•„์š”ํ•˜์—ฌ ์ œ์กฐ ์›๊ฐ€๊ฐ€ ๋†’์•„์งˆ ๋ฟ๋งŒ ์•„๋‹ˆ๋ผ ์œ„ํ—˜์š”์†Œ๋ฅผ ๊ฐ€์ง€๊ณ  ์žˆ๋‹ค.In addition, the bottle type sterilant supply system, once the bottle is installed once it can not be removed until it is used, since the inlet is destroyed after installation, there is a problem that the inconvenience and risk of removing the bottle, it is impossible to reuse . Moreover, additional systems are needed to collect and remove the remaining sterilizers, which increases manufacturing costs and poses risks.

๋˜ํ•œ, ๋ณ„๋„์˜ ๋‚ด๋ถ€ ์ €์žฅ๊ณต๊ฐ„์— ๋ฉธ๊ท ์ œ๋ฅผ ์ €์žฅํ•˜๋Š” ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์€ ๊ณผ์‚ฐํ™”์ˆ˜์†Œ์˜ ๊ฒฝ์šฐ ์˜ค์—ผ์— ๋งค์šฐ ์ทจ์•ฝํ•˜์—ฌ ๋†๋„๊ฐ€ ์ €ํ•˜๋˜๋Š” ๊ฒฝ์šฐ๊ฐ€ ์žˆ์œผ๋ฉฐ, ์•„์ฃผ ์ •๋ฐ€ํ•˜๊ฒŒ ์ •๋Ÿ‰์œผ๋กœ ์†Œ๋ถ„ํ•˜์—ฌ ๊ณต๊ธ‰ํ•˜๋Š” ๊ฒƒ์ด ์–ด๋ ต๊ณ , ๋ฉธ๊ท ์ œ๊ฐ€ ๋‚จ๊ฑฐ๋‚˜ ๋ชจ์ž๋ผ๋Š” ๊ฒฝ์šฐ ์ •๋Ÿ‰ ๊ณต๊ธ‰์ด ์–ด๋ ต๊ฒŒ ๋˜๋Š” ๋ฌธ์ œ์ ์„ ๊ฐ€์ง€๊ณ  ์žˆ์—ˆ๋‹ค.In addition, the sterilant supply system for storing the sterilant in a separate internal storage space is very susceptible to contamination in the case of hydrogen peroxide, the concentration may be lowered, it is difficult to supply by subdividing with a very precise quantitative, remaining or shortage of sterilant In this case, it was difficult to supply a fixed quantity.

์ด์™€ ๊ฐ™์€ ์ข…๋ž˜์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์—์„œ ๋ฉธ๊ท ์ œ๋“ค์˜ ์šด์†ก๊ณผ ๋ณด๊ด€์— ์žˆ์–ด์„œ, ๊ณผ์‚ฐํ™”์ˆ˜์†Œ์˜ ๊ฒฝ์šฐ ์ž์—ฐ ์••๋ ฅ์ด ๋ฐœ์ƒํ•˜๋ฏ€๋กœ ์šด์†ก ๋„์ค‘ ํญ๋ฐœ์ด๋‚˜ ๋†๋„ ์ €ํ•˜ ๋“ฑ์˜ ์œ„ํ—˜ ์š”์ธ์„ ๊ฐ€์ง€๊ณ  ์žˆ๊ธฐ ๋•Œ๋ฌธ์— ์šฉ๊ธฐ์™€ ํฌ์žฅ์— ํŠนํžˆ ์ฃผ์˜๋ฅผ ์š”ํ•œ๋‹ค.In the transport and storage of sterilants in such a conventional sterilant supply system, since hydrogen peroxide occurs due to the natural pressure, there is a risk factor, such as explosion or concentration drop during transportation requires special attention to containers and packaging.

์ƒ๊ธฐํ•œ ๋ฐ”์™€ ๊ฐ™์€ ์ข…๋ž˜์˜ ๋ฌธ์ œ์ ์„ ํ•ด๊ฒฐํ•˜๊ธฐ ์œ„ํ•˜์—ฌ, ๋ณธ ๋ฐœ๋ช…์€ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๊ฐ€ ๊ณผ์••๋ฐฉ์ง€ ๊ธฐ๋Šฅ์„ ๊ฐ€์ง์œผ๋กœ์จ, ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๊ฐ€ ๋’ค์ง‘ํ˜€ ์žˆ๋Š” ๋“ฑ ์–ด๋– ํ•œ ์ž์„ธ๋ผ๋„ ๊ฐ€์งˆ ์ˆ˜ ์žˆ๊ธฐ ๋•Œ๋ฌธ์— ์šด์†ก๊ณผ ๋ณด๊ด€์— ์šฉ์ดํ•˜๊ณ , ์žฅ์ฐฉ ์‹œ์—๋งŒ ๊ฐœ๋ฐฉ์ด ๋˜๋„๋ก ํ•จ๊ณผ ์•„์šธ๋Ÿฌ ํƒˆ์ฐฉ ์‹œ์—๋Š” ๋ฐ€ํ๊ฐ€ ๋˜๋„๋ก ํ•˜์—ฌ ์ทจ๊ธ‰์˜ ํŽธ๋ฆฌํ•จ๊ณผ ์•ˆ์ „์„ ๋„๋ชจํ•˜๋„๋ก ํ•œ๋‹ค.In order to solve the conventional problems as described above, the present invention is easy to transport and storage because the sterilant container has an overpressure preventing function, so that the sterilant container can be in any position such as upside down, and is easy to transport and store. In addition to being open, it should be sealed when it is detached to promote convenience and safety.

๋˜ํ•œ, ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๋กœ๋ถ€ํ„ฐ ๋ฉธ๊ท ์ œ์˜ ๊ณต๊ธ‰์„ ์œ„ํ•œ ๊ตฌ์„ฑ์ด ๊ฐ„๋‹จํ•˜๊ณ  ๋ฉธ๊ท ์ œ์˜ ๊ณต๊ธ‰์ด ์•ˆ์ •์ ์œผ๋กœ ์ด๋ฃจ์–ด์ง€๋„๋ก ํ•˜์—ฌ ์ œ์กฐ ์›๊ฐ€๋ฅผ ๋‚ฎ์ถ”๊ณ , ์ •๋Ÿ‰ ๊ณต๊ธ‰์˜ ์‹ ๋ขฐ์„ฑ์„ ๋†’์ด๋„๋ก ํ•œ๋‹ค.In addition, the configuration for supplying the sterilant from the sterilant container is simple and the supply of the sterilant is made to be stable to lower the manufacturing cost and to increase the reliability of the quantitative supply.

๋ณธ ๋ฐœ๋ช…์˜ ๋‹ค๋ฅธ ๋ชฉ์ ๋“ค์€ ์ดํ•˜์˜ ์‹ค์‹œ์˜ˆ์— ๋Œ€ํ•œ ์„ค๋ช…์„ ํ†ตํ•ด ์‰ฝ๊ฒŒ ์ดํ•ด๋  ์ˆ˜ ์žˆ์„ ๊ฒƒ์ด๋‹ค.Other objects of the present invention will be readily understood through the following description of the embodiments.

์ƒ๊ธฐํ•œ ๋ฐ”์™€ ๊ฐ™์€ ๋ชฉ์ ์„ ๋‹ฌ์„ฑํ•˜๊ธฐ ์œ„ํ•ด, ๋ณธ ๋ฐœ๋ช…์˜ ์ผ ์ธก๋ฉด์— ๋”ฐ๋ฅด๋ฉด, ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žฅ์ฐฉ๋˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์— ์žˆ์–ด์„œ, ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ฐ€ ์ €์žฅ๋˜๊ณ , ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ์˜ ์ฃผ์ž… ๋ฐ ๋ฐฐ์ถœ์„ ์œ„ํ•œ ์ถœ๊ตฌ๊ฐ€ ๋งˆ๋ จ๋˜๋Š” ์šฉ๊ธฐ; ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๋ฐ€ํ๋œ ์ƒํƒœ๋ฅผ ์œ ์ง€ํ•˜๋„๋ก ์ƒ๊ธฐ ์ถœ๊ตฌ์— ์„ค์น˜๋˜๊ณ , ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žฅ์ฐฉ์‹œ ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ; ๋ฐ ์ƒ๊ธฐ ์šฉ๊ธฐ์— ๋งˆ๋ จ๋˜๊ณ , ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ๊ณผ์••์„ ๋ฐฉ์ง€ํ•˜๊ธฐ ์œ„ํ•œ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์„ ํฌํ•จํ•˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๊ฐ€ ์ œ๊ณต๋œ๋‹ค.In order to achieve the above object, according to an aspect of the present invention, in the sterilant container mounted on the sterilant supply system of the sterilizer, the sterilant is stored, the outlet for the injection and discharge of the sterilant is A container provided; An automatic sealing valve installed at the outlet to maintain the outlet in a closed state and opening the outlet when mounted in the sterilant supply system; And a sterilant container provided in the container and including an overpressure preventing unit for preventing overpressure of the container.

์ƒ๊ธฐ ์šฉ๊ธฐ๋Š”, ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๊ฐ€ ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋„๋ก ์ผ์ธก์— ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์ด ํ˜•์„ฑ๋˜๊ณ , ์ƒ๊ธฐ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ์ƒ๊ธฐ ์ถœ๊ตฌ์ธก์˜ ๋ฐ˜๋Œ€์ธก๊ณผ ์ƒ๊ธฐ ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์˜ ๋‚ด์ธก์— ๊ฐ๊ฐ ๋งˆ๋ จ๋  ์ˆ˜ ์žˆ๋‹ค.The container may be provided with a valve interference prevention groove on one side such that the automatic sealing valve is located inside, and the overpressure prevention unit may be provided on the opposite side of the outlet side and inside the valve interference prevention groove, respectively.

๋ณธ ๋ฐœ๋ช…์˜ ๋‹ค๋ฅธ ์ธก๋ฉด์— ๋”ฐ๋ฅด๋ฉด, ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žˆ์–ด์„œ, ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ฐ€ ์ €์žฅ๋˜๋Š” ์šฉ๊ธฐ์™€, ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ์ถœ๊ตฌ์— ์„ค์น˜๋˜์–ด ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๋ฐ€ํ๋œ ์ƒํƒœ๋ฅผ ์œ ์ง€ํ•˜๋„๋ก ํ•จ๊ณผ ๋ˆ„๋ฆ„์— ์˜ํ•ด ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๋ฅผ ๊ฐ€์ง€๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ; ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ์— ์—ฐ๊ฒฐ๋˜๋„๋ก ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๊ฐ€ ์žฅ์ฐฉ๋˜๊ณ , ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๋ฅผ ๋ˆ„๋ฆ„์— ์˜ํ•ด ๊ฐœ๋ฐฉ์‹œ์ผœ์„œ ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์žฅ์ฐฉ๋ถ€; ์ƒ๊ธฐ ์ถœ๊ตฌ์—์„œ ๋ฐฐ์ถœ๋˜๋Š” ๋ฉธ๊ท ์ œ๋ฅผ ๋ฉธ๊ท ์ฑ”๋ฒ„๋กœ ๊ณต๊ธ‰ํ•˜๊ธฐ ์œ„ํ•œ ๊ฒฝ๋กœ๋ฅผ ์ œ๊ณตํ•˜๋Š” ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์— ์„ค์น˜๋˜๊ณ , ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์กฐ์ ˆํ•˜๋Š” ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›; ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์— ์„ค์น˜๋˜์–ด ๋ฉธ๊ท ์ œ์˜ ๊ณต๊ธ‰์„ ๊ฐœํ์‹œํ‚ค๋Š” ๊ฐœํ๋ฐธ๋ธŒ; ์ƒ๊ธฐ ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›์„ ํ†ต๊ณผํ•˜๋Š” ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์ธก์ •ํ•˜๋Š” ์ •๋Ÿ‰ํ™•์ธ์„ผ์„œ๋ฅผ ํ†ตํ•ด์„œ ๋ฉธ๊ท ์ œ๊ฐ€ ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์„ ํ†ตํ•ด ์ •๋Ÿ‰์œผ๋กœ ๊ณต๊ธ‰๋˜๋„๋ก ํ•˜๋Š” ์ •๋Ÿ‰์‹ค๋ฆฐ๋”; ๋ฐ ์ƒ๊ธฐ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”๋ฅผ ํ†ต๊ณผํ•œ ๋ฉธ๊ท ์ œ๋ฅผ ๊ธฐํ™”์‹œ์ผœ์„œ ์ƒ๊ธฐ ๋ฉธ๊ท ์ฑ”๋ฒ„์— ๊ณต๊ธ‰ํ•˜๋Š” ๊ธฐํ™”๊ธฐ๋ฅผ ํฌํ•จํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์ด ์ œ๊ณต๋œ๋‹ค.According to another aspect of the present invention, in the sterilant supply system of the sterilizer, the container in which the sterilant is stored, and installed in the outlet of the container to maintain the outlet is closed and the outlet is opened by pressing A sterilant container having an automatic sealing valve to enable; A sterilant container mounted to be connected to the automatic sealing valve, and a mounting part for opening the automatic sealing valve by pressing the automatic sealing valve to open the outlet; A flow rate control unit installed in a sterilant supply line providing a path for supplying a sterilant discharged from the outlet to a sterilization chamber, and controlling a flow rate of the sterilant; An on / off valve installed in the sterilant supply line to open and close the supply of the sterilant; A quantitative cylinder through which a sterilant is quantitatively supplied through the sterilant supply line through a quantitative confirmation sensor for measuring a flow rate of the sterilant passing through the flow control unit; And a sterilizer quantitative supply system of a sterilizer including a vaporizer which vaporizes the sterilant passed through the metering cylinder and supplies the sterilant to the sterilization chamber.

์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๋Š”, ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ์ผ์ธก์— ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๊ฐ€ ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋„๋ก ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์ด ํ˜•์„ฑ๋˜๊ณ , ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ๊ณผ์••์„ ๋ฐฉ์ง€ํ•˜๊ธฐ ์œ„ํ•˜์—ฌ ์ƒ๊ธฐ ์šฉ๊ธฐ์— ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ๋งˆ๋ จ๋˜๋ฉฐ, ์ƒ๊ธฐ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ์ƒ๊ธฐ ์ถœ๊ตฌ์ธก์˜ ๋ฐ˜๋Œ€์ธก๊ณผ ์ƒ๊ธฐ ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์˜ ๋‚ด์ธก์— ๊ฐ๊ฐ ๋งˆ๋ จ๋  ์ˆ˜ ์žˆ๋‹ค.The sterilant container, the valve interference prevention groove is formed so that the automatic sealing valve is located on one side of the container, the overpressure preventing unit is provided in the container to prevent the overpressure of the container, the overpressure preventing unit It may be provided on the opposite side of the outlet side and the inside of the valve interference prevention groove, respectively.

์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์—์„œ ์ƒ๊ธฐ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”์˜ ์ „๋‹จ์œผ๋กœ๋ถ€ํ„ฐ ๋ถ„๊ธฐ๋˜๋Š” ๋ถ„๊ธฐ๋ผ์ธ; ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์— ์„ค์น˜๋˜๋Š” ๋ฒคํŠธ๋ฐธ๋ธŒ; ๋ฐ ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์—์„œ ์ƒ๊ธฐ ๋ฒคํŠธ๋ฐธ๋ธŒ์˜ ํ›„๋‹จ์— ์„ค์น˜๋˜๊ณ , ๋ฏธ์ƒ๋ฌผ์ด๋‚˜ ์ด๋ฌผ์งˆ์ด ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์œผ๋กœ ์นจ์ž…ํ•˜๋Š” ์ฐจ๋‹จํ•˜๊ธฐ ์œ„ํ•œ ํ•„ํ„ฐ๋ฅผ ๋” ํฌํ•จํ•  ์ˆ˜ ์žˆ๋‹ค.Branch line branching from the front end of the metering cylinder in the sterilant supply line; A vent valve installed at the branch line; And installed at the rear end of the vent valve in the branch line, and may further include a filter for blocking microorganisms or foreign matter infiltrate into the branch line.

์ƒ๊ธฐ ์žฅ์ฐฉ๋ถ€๊ฐ€ ๋‚ด๋ถ€๊ณต๊ฐ„์— ์„ค์น˜๋˜๊ณ , ์ƒ๊ธฐ ๋‚ด๋ถ€๊ณต๊ฐ„์„ ๊ฐœํ์‹œํ‚ค๊ธฐ ์œ„ํ•œ ๋„์–ด๊ฐ€ ๋งˆ๋ จ๋˜๋Š” ์šฉ๊ธฐ์ฑ”๋ฒ„๋ฅผ ๋” ํฌํ•จํ•  ์ˆ˜ ์žˆ๋‹ค.The mounting unit may further include a container chamber installed in the inner space and provided with a door for opening and closing the inner space.

๋ณธ ๋ฐœ๋ช…์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ ๋ฐ ์ด๋ฅผ ์ด์šฉํ•œ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์˜ํ•˜๋ฉด, ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์˜ ์šด์†ก, ๋ณด๊ด€ ๋ฐ ์ทจ๊ธ‰์— ์žˆ์–ด์„œ ํŽธ๋ฆฌํ•จ๊ณผ ์•ˆ์ „ํ•จ์„ ์ œ๊ณตํ•˜๊ณ , ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์˜ ์žฌ์‚ฌ์šฉ์„ ๊ฐ€๋Šฅํ•˜๋„๋ก ํ•˜์—ฌ ๋น„์šฉ์„ ์ ˆ๊ฐํ•˜๋„๋ก ํ•˜๋ฉฐ, ๋ฉธ๊ท ์ œ๊ฐ€ ์ž”๋ฅ˜ํ•˜๊ฑฐ๋‚˜ ์†Œ์ง„ํ•œ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๋ฅผ ์ œ๊ฑฐํ•˜๊ธฐ ์œ„ํ•œ ์ถ”๊ฐ€ ์ œ๊ฑฐ ์‹œ์Šคํ…œ์„ ํ•„์š”๋กœ ํ•˜์ง€ ์•Š์•„ ์žฅ๋น„์˜ ๊ตฌ์„ฑ์ด ๊ฐ„๋‹จํ•ด์งˆ ๋ฟ๋งŒ ์•„๋‹ˆ๋ผ, ์ œ์กฐ ๋‹จ๊ฐ€๋ฅผ ๋‚ฎ์ถœ ์ˆ˜ ์žˆ๊ณ , ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์˜ 1ํšŒ ์žฅ์ฐฉ์œผ๋กœ ์—ฌ๋Ÿฌ ๋ฒˆ ๋ฉธ๊ท ์ œ์˜ ๊ณต๊ธ‰์„ ๊ฐ€๋Šฅํ•˜๋„๋ก ํ•œ๋‹ค.According to the sterilant container and the sterilant quantitative supply system of the sterilizer using the same according to the present invention, it provides convenience and safety in the transportation, storage and handling of the sterilant container, reducing the cost by enabling the reuse of the sterilant container It does not require an additional removal system to remove sterilant containers with residual or exhausted sterilant, which not only simplifies the construction of the equipment, but also lowers the manufacturing cost, and allows a single installation of the sterilant container several times. Allow the supply of sterile agents.

๋„ 1์€ ๋ณธ ๋ฐœ๋ช…์˜ ์ผ ์‹ค์‹œ์˜ˆ์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์„ ๋„์‹œํ•œ ๊ตฌ์„ฑ๋„์ด๊ณ ,1 is a block diagram showing a sterilant quantitative supply system of the sterilizer according to an embodiment of the present invention,

๋„ 2 ๋ฐ ๋„ 3์€ ๋ณธ ๋ฐœ๋ช…์˜ ์ผ ์‹ค์‹œ์˜ˆ์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๋ฅผ ๋„์‹œํ•œ ์‚ฌ์‹œ๋„์ด๊ณ ,2 and 3 is a perspective view showing a sterilant container according to an embodiment of the present invention,

๋„ 4๋Š” ๋ณธ ๋ฐœ๋ช…์˜ ์ผ ์‹ค์‹œ์˜ˆ์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์˜ ์šฉ๊ธฐ์ฑ”๋ฒ„๋ฅผ ๋„์‹œํ•œ ์‚ฌ์‹œ๋„์ด๋‹ค.Figure 4 is a perspective view showing a container chamber of the sterilant container according to an embodiment of the present invention.

๋ณธ ๋ฐœ๋ช…์€ ๋‹ค์–‘ํ•œ ๋ณ€๊ฒฝ์„ ๊ฐ€ํ•  ์ˆ˜ ์žˆ๊ณ , ์—ฌ๋Ÿฌ ๊ฐ€์ง€ ์‹ค์‹œ์˜ˆ๋ฅผ ๊ฐ€์งˆ ์ˆ˜ ์žˆ๋Š” ๋ฐ”, ํŠน์ • ์‹ค์‹œ์˜ˆ๋“ค์„ ๋„๋ฉด์— ์˜ˆ์‹œํ•˜๊ณ , ์ƒ์„ธํ•˜๊ฒŒ ์„ค๋ช…ํ•˜๊ณ ์ž ํ•œ๋‹ค. ๊ทธ๋Ÿฌ๋‚˜, ์ด๋Š” ๋ณธ ๋ฐœ๋ช…์„ ํŠน์ •ํ•œ ์‹ค์‹œ ํ˜•ํƒœ์— ๋Œ€ํ•ด ํ•œ์ •ํ•˜๋ ค๋Š” ๊ฒƒ์ด ์•„๋‹ˆ๊ณ , ๋ณธ ๋ฐœ๋ช…์˜ ๊ธฐ์ˆ  ์‚ฌ์ƒ ๋ฐ ๊ธฐ์ˆ  ๋ฒ”์œ„์— ํฌํ•จ๋˜๋Š” ๋ชจ๋“  ๋ณ€๊ฒฝ, ๊ท ๋“ฑ๋ฌผ ๋‚ด์ง€ ๋Œ€์ฒด๋ฌผ์„ ํฌํ•จํ•˜๋Š” ์‹์œผ๋กœ ์ดํ•ด ๋˜์–ด์•ผ ํ•˜๊ณ , ์—ฌ๋Ÿฌ ๊ฐ€์ง€ ๋‹ค๋ฅธ ํ˜•ํƒœ๋กœ ๋ณ€ํ˜•๋  ์ˆ˜ ์žˆ์œผ๋ฉฐ, ๋ณธ ๋ฐœ๋ช…์˜ ๋ฒ”์œ„๊ฐ€ ํ•˜๊ธฐ ์‹ค์‹œ์˜ˆ์— ํ•œ์ •๋˜๋Š” ๊ฒƒ์€ ์•„๋‹ˆ๋‹ค. As the inventive concept allows for various changes and numerous embodiments, particular embodiments will be illustrated in the drawings and described in detail in the written description. However, this is not intended to limit the present invention to specific embodiments, but should be understood as including all changes, equivalents, and substitutes included in the spirit and scope of the present invention, and may be modified in various other forms. It is to be understood that the scope of the present invention is not limited to the following examples.

์ดํ•˜, ์ฒจ๋ถ€๋œ ๋„๋ฉด์„ ์ฐธ์กฐํ•˜์—ฌ ๋ณธ ๋ฐœ๋ช…์— ๋”ฐ๋ฅธ ์‹ค์‹œ์˜ˆ๋ฅผ ์ƒ์„ธํžˆ ์„ค๋ช…ํ•˜๋ฉฐ, ๋„๋ฉด ๋ถ€ํ˜ธ์— ๊ด€๊ณ„์—†์ด ๋™์ผํ•˜๊ฑฐ๋‚˜ ๋Œ€์‘ํ•˜๋Š” ๊ตฌ์„ฑ์š”์†Œ์— ๋Œ€ํ•ด์„œ๋Š” ๋™์ผํ•œ ์ฐธ์กฐ ๋ฒˆํ˜ธ๋ฅผ ๋ถ€์—ฌํ•˜๊ณ , ์ด์— ๋Œ€ํ•ด ์ค‘๋ณต๋˜๋Š” ์„ค๋ช…์„ ์ƒ๋žตํ•˜๊ธฐ๋กœ ํ•œ๋‹ค.Hereinafter, exemplary embodiments of the present invention will be described in detail with reference to the accompanying drawings, and the same or corresponding components will be given the same reference numerals regardless of the reference numerals, and redundant description thereof will be omitted.

๋„ 1์€ ๋ณธ ๋ฐœ๋ช…์˜ ์ผ ์‹ค์‹œ์˜ˆ์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์„ ๋„์‹œํ•œ ๊ตฌ์„ฑ๋„์ด๋‹ค. 1 is a block diagram showing a sterilant quantitative supply system of the sterilizer according to an embodiment of the present invention.

๋„ 1์— ๋„์‹œ๋œ ๋ฐ”์™€ ๊ฐ™์ด, ๋ณธ ๋ฐœ๋ช…์˜ ์ผ ์‹ค์‹œ์˜ˆ์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ(100)์€ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)์™€, ์žฅ์ฐฉ๋ถ€(120)์™€, ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›(130)๊ณผ, ๊ฐœํ๋ฐธ๋ธŒ(140,170,190)์™€, ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์™€, ๊ธฐํ™”๊ธฐ(180)๋ฅผ ํฌํ•จํ•  ์ˆ˜ ์žˆ๋‹ค. ํ•œํŽธ, ๋ณธ ๋ฐœ๋ช…์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ(100)์—์„œ ํ•จ๊ป˜ ์„ค๋ช…ํ•˜๊ธฐ๋กœ ํ•œ๋‹ค. As shown in Figure 1, the sterilant quantitative supply system 100 of the sterilizer according to an embodiment of the present invention is a sterilant container 110, the mounting portion 120, the flow control unit 130, opening and closing The valves 140, 170, and 190 may include a metering cylinder 150 and a vaporizer 180. On the other hand, the sterilant container 110 according to the present invention will be described together in the sterilant quantitative supply system 100 of the sterilizer.

๋„ 2 ๋ฐ ๋„ 3์— ๋„์‹œ๋œ ๋ฐ”์™€ ๊ฐ™์ด, ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)๋Š” ์šฉ๊ธฐ(111)์™€ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)๋ฅผ ํฌํ•จํ•˜๊ณ , ๋‚˜์•„๊ฐ€์„œ, ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›(113)์„ ๋” ํฌํ•จํ•  ์ˆ˜ ์žˆ๋‹ค.As shown in FIG. 2 and FIG. 3, the sterilant container 110 may include a container 111 and an automatic sealing valve 112, and further include an overpressure preventing unit 113.

์šฉ๊ธฐ(111)๋Š” ๋ฉธ๊ท ์ œ, ์˜ˆ์ปจ๋Œ€ ๊ณผ์‚ฐํ™”์ˆ˜์†Œ๊ฐ€ ๋‚ด์ธก์— ์ €์žฅ๋˜๊ณ , ๋ฉธ๊ท ์ œ์˜ ์ฃผ์ž… ๋ฐ ๋ฐฐ์ถœ์„ ์œ„ํ•œ ์ถœ๊ตฌ(๋ฏธ๋„์‹œ)๊ฐ€ ๋งˆ๋ จ๋˜๊ณ , ๋ฉธ๊ท ์ œ์˜ ์••๋ ฅ์— ๊ฒฌ๋””๊ธฐ ์œ„ํ•œ ์žฌ์งˆ๋กœ ์ด๋ฃจ์–ด์ง€๋ฉฐ, ๋ณธ ์‹ค์‹œ์˜ˆ์—์„œ์ฒ˜๋Ÿผ ์›ํ˜• ์šฉ๊ธฐ๋Š” ๋ฌผ๋ก  ๋‹ค์–‘ํ•œ ํ˜•์ƒ์„ ๊ฐ€์งˆ ์ˆ˜ ์žˆ๋‹ค.The container 111 is a sterilant, for example, hydrogen peroxide is stored therein, an outlet (not shown) for injecting and discharging the sterilant is provided, and is made of a material to withstand the pressure of the sterilant, and as shown in the embodiment The container can of course have various shapes.

์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)๋Š” ์šฉ๊ธฐ(111)์˜ ์ถœ๊ตฌ๊ฐ€ ๋ฐ€ํ๋œ ์ƒํƒœ๋ฅผ ์œ ์ง€ํ•˜๋„๋ก ์ถœ๊ตฌ์— ์„ค์น˜๋˜๊ณ , ์ผ๋ก€๋กœ ๋ˆ„๋ฆ„ ์ž‘์šฉ์— ์˜ํ•ด ์ถœ๊ตฌ๋ฅผ ๊ฐœ๋ฐฉ์‹œํ‚ค๋„๋ก ํ•˜๋Š”๋ฐ, ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ(100)์˜ ์žฅ์ฐฉ๋ถ€(120)์— ์žฅ์ฐฉ์‹œ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•œ๋‹ค. ํ•œํŽธ, ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)๋Š” ๋‚ด์ธก์˜ ์‹ค๋ง๋ถ€์žฌ๊ฐ€ ์Šคํ”„๋ง์˜ ํƒ„์„ฑ๋ ฅ์— ์˜ํ•ด ์œ ๋กœ๋ฅผ ํ์‡„์‹œํ‚ด์œผ๋กœ์จ ์šฉ๊ธฐ(111)์˜ ์ถœ๊ตฌ๋ฅผ ๋ฐ€ํ์‹œํ‚ค๊ณ , ์žฅ์ฐฉ๋ถ€(120)์— ์žฅ์ฐฉ์‹œ ์žฅ์ฐฉ๋ถ€(120)์˜ ํ•€์— ์˜ํ•ด ์‹ค๋ง๋ถ€์žฌ๊ฐ€ ๋ˆŒ๋ ค์ ธ์„œ ์Šคํ”„๋ง์„ ๋ˆ„๋ฅด๋ฉด์„œ ์œ ๋กœ๊ฐ€ ๊ฐœ๋ฐฉ๋จ์œผ๋กœ์จ ์šฉ๊ธฐ(111)์˜ ์ถœ๊ตฌ๋ฅผ ๊ฐœ๋ฐฉ์‹œํ‚ค๋„๋ก ํ•œ๋‹ค.The automatic sealing valve 112 is installed at the outlet to maintain the outlet of the container 111 in a closed state, for example to open the outlet by pressing action, the mounting portion 120 of the sterilant supply system 100 Make sure the outlet is open when mounted on On the other hand, the automatic sealing valve 112 seals the outlet of the container 111 by closing the flow path by the inner sealing member by the elastic force of the spring, the sealing member by the pin of the mounting portion 120 when mounted on the mounting portion 120 Is pressed to open the outlet of the container 111 by opening the flow path while pressing the spring.

๊ณผ์••๋ฐฉ์ง€์œ ๋‹›(113)์€ ์šฉ๊ธฐ(111)์— ๋งˆ๋ จ๋˜๊ณ , ์šฉ๊ธฐ(111)์˜ ๊ณผ์••์„ ๋ฐฉ์ง€ํ•˜๋„๋ก ํ•˜๋Š”๋ฐ, ์ผ๋ก€๋กœ ์šฉ๊ธฐ(111) ๋‚ด์˜ ์••๋ ฅ์ด ์ •ํ•ด์ง„ ์••๋ ฅ ์ด์ƒ์ผ ๊ฒฝ์šฐ ์ฐจ๋‹จ๋ถ€์žฌ๊ฐ€ ์Šคํ”„๋ง์˜ ์••์ถ•์— ์˜ํ•ด ์šฉ๊ธฐ(111)์˜ ๋ฐฐ์ถœ๊ตฌ๋ฅผ ๊ฐœ๋ฐฉ์‹œํ‚ด์œผ๋กœ์จ ์šฉ๊ธฐ(111)๊ฐ€ ์ •ํ•ด์ง„ ์••๋ ฅ ์ด์ƒ์ด ๋˜์ง€ ์•Š๋„๋ก ํ•˜๊ณ , ์šฉ๊ธฐ(111) ๋‚ด์˜ ์••๋ ฅ์ด ์ •ํ•ด์ง„ ์••๋ ฅ ๋ฏธ๋งŒ์ผ ๊ฒฝ์šฐ ์ฐจ๋‹จ๋ถ€์žฌ๊ฐ€ ์Šคํ”„๋ง์˜ ํŒฝ์ฐฝ์— ์˜ํ•ด ์šฉ๊ธฐ(111)์˜ ๋ฐฐ์ถœ๊ตฌ๋ฅผ ๋ฐ€ํ์‹œํ‚ค๋„๋ก ๊ตฌ์„ฑ๋  ์ˆ˜ ์žˆ์œผ๋ฉฐ, ์ด์™€ ๋‹ฌ๋ฆฌ ๋‹ค๋ฅธ ์˜ˆ๋กœ์„œ, ์šฉ๊ธฐ(111) ๋‚ด์ธก์— ์„ค์น˜๋˜๊ณ , ์šฉ๊ธฐ(111) ๋‚ด์˜ ์••๋ ฅ์ด ์ •ํ•ด์ง„ ์••๋ ฅ ์ด์ƒ์ผ ๊ฒฝ์šฐ ์ฐจ๋‹จ๋ถ€์žฌ๊ฐ€ ์Šคํ”„๋ง์„ ์••์ถ•์‹œ์ผœ์„œ ์šฉ๊ธฐ(111) ๋‚ด์— ๋งˆ๋ จ๋œ ๋ฐ€ํ๊ณต๊ฐ„ ๋‚ด์ธก์œผ๋กœ ์ด๋™ํ•˜์—ฌ ์šฉ๊ธฐ(111) ๋‚ด์˜ ์ฒด์ ์ด ์ฆ๊ฐ€ํ•˜๋„๋ก ํ•˜๊ณ , ์šฉ๊ธฐ(111) ๋‚ด์˜ ์••๋ ฅ์ด ์ •ํ•ด์ง„ ์••๋ ฅ ๋ฏธ๋งŒ์ผ ๊ฒฝ์šฐ ์ฐจ๋‹จ๋ถ€์žฌ๊ฐ€ ์Šคํ”„๋ง์— ์˜ํ•ด ๋ฐ€ํ๊ณต๊ฐ„ ์™ธ์ธก์œผ๋กœ ์ด๋™ํ•˜์—ฌ ์šฉ๊ธฐ(111) ๋‚ด์˜ ์ฒด์ ์ด ๊ฐ์†Œํ•˜๋„๋ก ๊ตฌ์„ฑ๋  ์ˆ˜ ์žˆ๋‹ค.The overpressure preventing unit 113 is provided in the container 111 and prevents overpressure of the container 111. For example, when the pressure in the container 111 is equal to or greater than a predetermined pressure, the blocking member is compressed by the spring 111. By opening the outlet of the) to prevent the container 111 from being above a predetermined pressure, and when the pressure in the container 111 is less than the predetermined pressure, the blocking member is configured to seal the outlet of the container 111 by expansion of the spring. Alternatively, as another example, the container 111 is installed inside the container 111, and when the pressure in the container 111 is greater than or equal to a predetermined pressure, the blocking member compresses the spring to move inside the sealed space provided in the container 111 to store the container ( When the volume in the container 111 is increased, and the pressure in the container 111 is less than the predetermined pressure, the blocking member is moved out of the closed space by a spring so that the volume in the container 111 decreases. The lock may be configured.

์šฉ๊ธฐ(111)๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)๊ฐ€ ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋„๋ก ์ผ์ธก์— ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ(114)์ด ํ˜•์„ฑ๋˜๊ณ , ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›(113)์ด ์ถœ๊ตฌ์ธก์˜ ๋ฐ˜๋Œ€์ธก๊ณผ ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ(114)์˜ ๋‚ด์ธก์— ๊ฐ๊ฐ ๋‹ค์ˆ˜๋กœ ๋งˆ๋ จ๋  ์ˆ˜ ์žˆ๋‹ค.The container 111 has a valve interference preventing groove 114 formed at one side such that the automatic sealing valve 112 is located inside, and the overpressure preventing unit 113 has an opposite side of the outlet side and an inner side of the valve interference preventing groove 114. Each may be provided in plurality.

์žฅ์ฐฉ๋ถ€(120)๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)์— ์—ฐ๊ฒฐ๋˜๋„๋ก ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)๊ฐ€ ์žฅ์ฐฉ๋˜๊ณ , ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)์˜ ์ฃผ์ž…๊ตฌ์— ๋‚˜์‚ฌ๊ฒฐํ•ฉ๋  ์ˆ˜ ์žˆ์œผ๋ฉฐ, ์ผ๋ก€๋กœ ํ•€์— ์˜ํ•ด์„œ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)๋ฅผ ๋ˆ„๋ฆ„์— ์˜ํ•ด ๊ฐœ๋ฐฉ์‹œ์ผœ์„œ ์šฉ๊ธฐ(111)์˜ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜์—ฌ ๋ฉธ๊ท ์ œ์˜ ๋ฐฐ์ถœ์ด ๊ฐ€๋Šฅํ•˜๋„๋ก ํ•œ๋‹ค.Mounting unit 120 is equipped with a sterilant container 110 to be connected to the automatic sealing valve 112, it may be screwed to the inlet of the automatic sealing valve 112, for example, the automatic sealing valve 112 by a pin By pressing to open the outlet of the container 111 is opened to enable the discharge of the sterilant.

์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›(130)์€ ์ถœ๊ตฌ์—์„œ ๋ฐฐ์ถœ๋˜๋Š” ๋ฉธ๊ท ์ œ๋ฅผ ๋ฉธ๊ท ์ฑ”๋ฒ„(10)๋กœ ๊ณต๊ธ‰ํ•˜๊ธฐ ์œ„ํ•œ ๊ฒฝ๋กœ๋ฅผ ์ œ๊ณตํ•˜๋Š” ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ(210)์— ์„ค์น˜๋˜๊ณ , ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์กฐ์ ˆํ•œ๋‹ค. ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›(130)์€ ์ผ๋ก€๋กœ ์œ ๋Ÿ‰์กฐ์ ˆ๋ฐธ๋ธŒ๋กœ ์ด๋ฃจ์–ด์งˆ ์ˆ˜ ์žˆ๊ณ , ์ด๋Ÿฌํ•œ ๋ฐธ๋ธŒ๊ฐ€ ๋ฉ”๋‰ด์–ผ ๋ฐธ๋ธŒ๋กœ ์ด๋ฃจ์–ด์ง€๊ฑฐ๋‚˜, ์ œ์–ด์‹ ํ˜ธ์— ๋”ฐ๋ผ ๋™์ž‘ํ•˜๋Š” ์ œ์–ด๋ฐธ๋ธŒ๋กœ ์ด๋ฃจ์–ด์งˆ ์ˆ˜ ์žˆ๋‹ค. ์—ฌ๊ธฐ์„œ, ๋ฉธ๊ท ์ฑ”๋ฒ„(10)๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ์ผ๋ถ€๋ฅผ ์ด๋ฃจ๊ฒŒ ๋˜๊ณ , ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋Š” ๋ฉธ๊ท ๋Œ€์ƒ๋ฌผ์ด ๋ฉธ๊ท ์ œ์— ์˜ํ•ด ๋ฉธ๊ท ๋˜๋„๋ก ํ•˜๋Š” ๋ฐ€ํ ๊ณต๊ฐ„์„ ์ œ๊ณตํ•œ๋‹ค.Flow control unit 130 is installed in the sterilant supply line 210 to provide a path for supplying the sterilant discharged from the outlet to the sterilization chamber 10, and adjusts the flow rate of the sterilant. The flow control unit 130 may be made of, for example, a flow control valve, and the valve may be made of a manual valve or a control valve that operates according to a control signal. Here, the sterilization chamber 10 forms a part of the sterilizer, and provides a closed space for sterilization objects located inside to be sterilized by the sterilizing agent.

๊ฐœํ๋ฐธ๋ธŒ(140,170,190)๋Š” ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ(210)์— ์„ค์น˜๋˜์–ด ๋ฉธ๊ท ์ œ์˜ ๊ณต๊ธ‰์„ ๊ฐœํ์‹œํ‚ค๋Š”๋ฐ, ์ œ์–ด์‹ ํ˜ธ์— ๋”ฐ๋ผ ๋™์ž‘ํ•˜๋Š” ์ œ์–ด๋ฐธ๋ธŒ๋กœ ์ด๋ฃจ์–ด์งˆ ์ˆ˜ ์žˆ๊ณ , ๋‹จ์ผ๋กœ ์ด๋ฃจ์–ด์ง€๊ฑฐ๋‚˜, ๋ณธ ์‹ค์‹œ์˜ˆ์—์„œ์ฒ˜๋Ÿผ ์œ ๋Ÿ‰์‹ค๋ฆฐ๋”(150)์˜ ์ „๋‹จ๊ณผ ํ›„๋‹จ, ๊ทธ๋ฆฌ๊ณ  ๋ฉธ๊ท ์ฑ”๋ฒ„(10)์˜ ์ „๋‹จ์— ๊ฐ๊ฐ ์„ค์น˜๋จ์œผ๋กœ์จ ์œ ๋Ÿ‰์‹ค๋ฆฐ๋”(140), ๊ธฐํ™”๊ธฐ(180), ๊ทธ๋ฆฌ๊ณ  ๋ฉธ๊ท ์ฑ”๋ฒ„(10)๋กœ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰์„ ๊ฐ๊ฐ ๊ฐœํ์‹œํ‚ฌ ์ˆ˜ ์žˆ๋‹ค.Opening / closing valves 140, 170, and 190 are installed in the sterilant supply line 210 to open and close the supply of the sterilant, and may be made of a control valve operating in accordance with a control signal, made of a single, or flow cylinder 150 as in this embodiment By being installed at the front and rear ends of the) and the front end of the sterilization chamber 10, the sterilant supply to the flow cylinder 140, the vaporizer 180, and the sterilization chamber 10 can be opened and closed, respectively.

์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)๋Š” ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›(130)์„ ํ†ต๊ณผํ•˜๋Š” ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์ธก์ •ํ•˜๋Š” ์ •๋Ÿ‰ํ™•์ธ์„ผ์„œ(160)๋ฅผ ํ†ตํ•ด์„œ ๋ฉธ๊ท ์ œ๊ฐ€ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ(210)์„ ํ†ตํ•ด ์ •๋Ÿ‰์œผ๋กœ ๊ณต๊ธ‰๋˜๋„๋ก ํ•˜๋Š”๋ฐ, ์ผ๋ก€๋กœ ์ „๋‹จ๊ณผ ํ›„๋‹จ์— ๊ฐ๊ฐ ์„ค์น˜๋˜๋Š” ๊ฐœํ๋ฐธ๋ธŒ(140,170)์˜ ๊ฐœํ๋™์ž‘์— ์˜ํ•ด์„œ, ์™ธ๋ถ€๋กœ๋ถ€ํ„ฐ ๊ณต๊ธ‰๋˜๋Š” ์ง„๊ณต์ด ๋‚ด์ธก์— ์ฑ„์›Œ์ง€๊ณ , ์ด๋Ÿฌํ•œ ์ง„๊ณต์— ์˜ํ•ด ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)๋กœ๋ถ€ํ„ฐ ๋ฉธ๊ท ์ œ๊ฐ€ ์œ ์ž…๋˜๋„๋ก ํ•˜๋ฉฐ, ๋‚ด์ธก์— ์ฑ„์›Œ์ง„ ๋ฉธ๊ท ์ œ๊ฐ€ ์ €์••์„ ํ˜•์„ฑํ•˜๋Š” ๊ธฐํ™”๊ธฐ(180) ์ธก์œผ๋กœ ๊ณต๊ธ‰๋˜๋„๋ก ํ•œ๋‹ค. ํ•œํŽธ, ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์— ๋งˆ๋ จ๋˜๊ฑฐ๋‚˜ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์™€๋Š” ๋ณ„๊ฐœ๋กœ ์ด๋ฃจ์–ด์ง€๋Š” ์ œ์–ด๋ถ€(๋ฏธ๋„์‹œ)๋Š” ์ •๋Ÿ‰ํ™•์ธ์„ผ์„œ(160)๋ฅผ ํ†ตํ•ด์„œ ๊ฐ์ง€๋˜๋Š” ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์‚ฐ์ถœํ•˜์—ฌ ๋ฉธ๊ท ์ œ๊ฐ€ ์ •๋Ÿ‰์œผ๋กœ ๊ณต๊ธ‰๋˜๋„๋ก ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์˜ ๋™์ž‘์„ ์ œ์–ดํ•˜๊ฒŒ ๋˜๊ณ , ๋‚˜์•„๊ฐ€์„œ, ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์— ์˜ํ•œ ๋ฉธ๊ท ์ œ์˜ ์ •๋Ÿ‰ ๊ณต๊ธ‰์„ ์œ„ํ•˜์—ฌ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์˜ ์ „๋‹จ๊ณผ ํ›„๋‹จ์— ๊ฐ๊ฐ ์„ค์น˜๋˜๋Š” ๊ฐœํ๋ฐธ๋ธŒ(140,170)๋ฅผ ๊ฐ๊ฐ ์ œ์–ดํ•  ์ˆ˜ ์žˆ๋‹ค. The metering cylinder 150 is to be supplied in a quantitative manner through the sterilant supply line 210 through the quantitative confirmation sensor 160 for measuring the flow rate of the sterilant passing through the flow control unit 130, for example shear By opening and closing operations of the opening and closing valves 140 and 170 respectively installed at the rear and rear ends, the vacuum supplied from the outside is filled inside, and the sterilizing agent is introduced from the sterilant container 110 by the vacuum, and the sterilizing agent filled inside is It is to be supplied to the vaporizer 180 to form a low pressure. On the other hand, the control unit (not shown) provided in the quantitative cylinder 150 or separate from the quantitative cylinder 150 calculates the flow rate of the sterilant detected through the quantitative confirmation sensor 160 so that the sterilant is supplied in a quantitative manner. The operation of the 150 may be controlled, and further, the open / close valves 140 and 170 respectively installed at the front and rear ends of the metering cylinder 150 may be controlled to supply the metered amount of the sterilant by the metering cylinder 150, respectively. .

๊ธฐํ™”๊ธฐ(180)๋Š” ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)๋ฅผ ํ†ต๊ณผํ•œ ๋ฉธ๊ท ์ œ๋ฅผ ๊ธฐํ™”์‹œ์ผœ์„œ ๋ฉธ๊ท ์ฑ”๋ฒ„(10)์— ๊ณต๊ธ‰ํ•จ์œผ๋กœ์จ ๋ฉธ๊ท ์ฑ”๋ฒ„(10)์— ๋ฉธ๊ท ์ œ๊ฐ€ ๊ธฐํ™”์ƒํƒœ๋กœ ๊ณต๊ธ‰๋˜์–ด ๋ฉธ๊ท  ์ž‘์šฉ์ด ์›ํ™œํ•˜๊ฒŒ ์ด๋ฃจ์–ด์ง€๋„๋ก ํ•œ๋‹ค. ํ•œํŽธ, ๊ธฐํ™”๊ธฐ(180)๋Š” ์—ด์˜ ์ œ๊ณต์ด๋‚˜ ์••๋ ฅ ์ €ํ•˜๋ฅผ ํ†ตํ•ด์„œ ๋ฉธ๊ท ์ œ๊ฐ€ ๊ธฐํ™”๋˜๋„๋ก ํ•  ์ˆ˜ ์žˆ๋‹ค.The vaporizer 180 vaporizes the sterilant passed through the metering cylinder 150 and supplies it to the sterilization chamber 10 so that the sterilizing agent is supplied to the sterilization chamber 10 in a vaporized state so that the sterilization operation is smoothly performed. Meanwhile, the vaporizer 180 may allow the sterilizing agent to be vaporized by providing heat or lowering the pressure.

๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ(210)์—๋Š” ๋ถ„๊ธฐ๋ผ์ธ(220)์ด ๋ถ„๊ธฐ๋  ์ˆ˜ ์žˆ๋Š”๋ฐ, ์ด๋Ÿฌํ•œ ๋ถ„๊ธฐ๋ผ์ธ(220)์€ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ(210)์—์„œ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์˜ ์ „๋‹จ์œผ๋กœ๋ถ€ํ„ฐ ๋ถ„๊ธฐ๋˜๋„๋ก ๋งˆ๋ จ๋˜๊ณ , ๋ฒคํŠธ๋ฐธ๋ธŒ(vent valve; 230) ๋ฐ ํ•„ํ„ฐ(filter; 240)๊ฐ€ ์„ค์น˜๋œ๋‹ค.Branch line 220 may be branched to the sterilant supply line 210, this branch line 220 is provided to branch from the front end of the metering cylinder 150 in the sterilant supply line 210, vent valve ( vent valve 230 and filter 240 are installed.

๋ฒคํŠธ๋ฐธ๋ธŒ(230)๋Š” ์ผ๋ก€๋กœ ์ œ์–ด์‹ ํ˜ธ์— ์˜ํ•ด ๋™์ž‘ํ•˜๋Š” ์ œ์–ด๋ฐธ๋ธŒ๋กœ ์ด๋ฃจ์–ด์งˆ ์ˆ˜ ์žˆ๊ณ , ๊ฐœ๋ฐฉ๋จ์œผ๋กœ์จ ๋ถ„๊ธฐ๋ผ์ธ(220)์„ ํ†ตํ•œ ๋ฉธ๊ท ์ œ์˜ ๋ฐฐ์ถœ์„ ๊ฐ€๋Šฅํ•˜๋„๋ก ํ•œ๋‹ค.The vent valve 230 may be formed of, for example, a control valve operated by a control signal, and may be opened to allow the sterilant to be discharged through the branch line 220.

ํ•„ํ„ฐ(240)๋Š” ๋ถ„๊ธฐ๋ผ์ธ(220)์—์„œ ๋ฒคํŠธ๋ฐธ๋ธŒ(230)์˜ ํ›„๋‹จ์— ์„ค์น˜๋˜๊ณ , ๋ฏธ์ƒ๋ฌผ์ด๋‚˜ ์ด๋ฌผ์งˆ์ด ๋ถ„๊ธฐ๋ผ์ธ(220)์œผ๋กœ ์นจ์ž…ํ•˜๋Š” ๊ฒƒ์„ ์ฐจ๋‹จํ•˜๋„๋ก ํ•˜๋Š”๋ฐ, ์ผ๋ก€๋กœ ๋ฐ•ํ…Œ๋ฆฌ์•„ํ•„ํ„ฐ๊ฐ€ ์‚ฌ์šฉ๋  ์ˆ˜ ์žˆ๋‹ค.The filter 240 is installed at the rear end of the vent valve 230 in the branch line 220 to block the invasion of microorganisms or foreign substances into the branch line 220, for example, a bacterial filter may be used.

๋„ 4์— ๋„์‹œ๋œ ๋ฐ”์™€ ๊ฐ™์ด, ์žฅ์ฐฉ๋ถ€(120)๋Š” ์šฉ๊ธฐ์ฑ”๋ฒ„(250)์˜ ๋‚ด์ธก์— ์„ค์น˜๋  ์ˆ˜ ์žˆ๋Š”๋ฐ, ์ด๋Ÿฌํ•œ ์šฉ๊ธฐ์ฑ”๋ฒ„(250)๋Š” ์žฅ์ฐฉ๋ถ€(120)๊ฐ€ ์„ค์น˜๋˜๊ธฐ ์œ„ํ•œ ๋‚ด๋ถ€๊ณต๊ฐ„(251)์„ ๊ฐ€์ง€๊ณ , ๋‚ด๋ถ€๊ณต๊ฐ„(251)์„ ๊ฐœํ์‹œํ‚ค๊ธฐ ์œ„ํ•œ ๋„์–ด(252)๊ฐ€ ํžŒ์ง€ ๊ฒฐํ•ฉ์— ์˜ํ•ด ๋งˆ๋ จ๋˜๊ณ , ๋„์–ด(252)์˜ ๋กํ‚น ๋ฐ ์–ธ๋กํ‚น์„ ์œ„ํ•˜์—ฌ ๋„์–ด(252)์˜ ์ผ์ธก๊ณผ ์ด์— ๋งˆ์ฃผํ•˜๋Š” ์ธก์— ๋กํ‚น๋ถ€์žฌ(253)๊ฐ€ ๋งˆ๋ จ๋œ๋‹ค.As shown in FIG. 4, the mounting part 120 may be installed inside the container chamber 250, and the container chamber 250 may have an inner space 251 for mounting the mounting part 120. A door 252 for opening and closing the space 251 is provided by a hinge coupling, and a locking member 253 is provided on one side of the door 252 and the side facing the door 252 for locking and unlocking the door 252. do.

์ด์™€ ๊ฐ™์€ ๋ณธ ๋ฐœ๋ช…์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ ๋ฐ ์ด๋ฅผ ์ด์šฉํ•œ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์˜ํ•˜๋ฉด, ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)๋Š” ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›(113)์— ์˜ํ•ด์„œ, ์–ด๋– ํ•œ ์ž์„ธ๋กœ ์„ค์น˜๋˜๋”๋ผ๋„ ๊ณผ์‚ฐํ™”์ˆ˜์†Œ์™€ ๊ฐ™์€ ๋ฉธ๊ท ์ œ์˜ ์ž์—ฐ ๋ถ„ํ•ด์— ์˜ํ•ด ์••๋ ฅ์ด ์ฆ๊ฐ€ํ•œ๋‹ค๊ณ  ํ•˜๋”๋ผ๋„ ์šด์†ก, ๋ณด๊ด€, ์ทจ๊ธ‰ ๋“ฑ์ด ์šฉ์ดํ•˜๋„๋ก ํ•˜๊ณ , ์•ˆ์ „์„ฑ์„ ๋†’์ผ ์ˆ˜ ์žˆ๋‹ค.According to the sterilant container according to the present invention and the sterilant quantitative supply system of the sterilizer using the same, the sterilant container 110 by the overpressure prevention unit 113, even if installed in any position, the nature of the sterilant such as hydrogen peroxide Even if the pressure increases due to decomposition, it is easy to transport, store, handle, etc., and the safety can be improved.

๋˜ํ•œ, ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ(112)์— ์˜ํ•ด ์žฅ์ฐฉ๋ถ€(120)์— ์žฅ์ฐฉ ์‹œ์—๋งŒ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๊ณ , ์žฅ์ฐฉ๋ถ€(120)์— ํƒˆ์ฐฉ ์‹œ์—๋Š” ๋ฐ€ํ๋˜๋„๋ก ํ•จ์œผ๋กœ์จ ์‚ฌ์šฉ์ค‘์ด๊ฑฐ๋‚˜ ์‚ฌ์šฉ ํ›„ ์ œ๊ฑฐํ•˜๋Š”๋ฐ ์žˆ์–ด ๋ณ„๋„์˜ ์žฅ์น˜๊ฐ€ ํ•„์š”ํ•˜์ง€ ์•Š๋‹ค.In addition, the sterilant container 110 is to be opened only when mounted to the mounting portion 120 by the automatic sealing valve 112, and to be sealed when detached to the mounting portion 120 to separate the device in use or removed after use Is not necessary.

๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)๋Š” ์žฅ์ฐฉ๋ถ€(120)์— ์žฅ์ฐฉ๋  ๊ฒฝ์šฐ ๋ณ„๋„์˜ ๋‚ด๋ถ€ ์ €์žฅ๊ณต๊ฐ„์ด ์—†์–ด๋„ ๋˜๊ณ , ๊ทธ ์ž์ฒด๊ฐ€ ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ €์žฅ ๊ณต๊ฐ„์ด ๋˜๋„๋ก ํ•œ๋‹ค. When the sterilant container 110 is mounted on the mounting portion 120, there is no need for a separate internal storage space, so that the sterilant storage space of the sterilizer itself.

๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ(100)์€ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์— ์ง„๊ณต์„ ํ˜•์„ฑ์‹œํ‚ค๊ณ , ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150) ์ „.ํ›„๋‹จ์˜ ๊ฐœํ๋ฐธ๋ธŒ(140,170)๋ฅผ ์ด์šฉํ•˜์—ฌ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)๋ฅผ ๋ฐ€ํํ•œ ๋‹ค์Œ, ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150) ์ „๋‹จ์˜ ๊ฐœํ๋ฐธ๋ธŒ(140)๋ฅผ ๊ฐœ๋ฐฉ์‹œ์ผœ์„œ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)์— ๋ฉธ๊ท ์ œ๋ฅผ ์›ํ•˜๋Š” ์–‘๋งŒํผ ์ฑ„์šฐ๊ฒŒ ๋œ๋‹ค. ์ด๋•Œ, ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ(110)์™€ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150) ์‚ฌ์ด์— ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›(130)์ด ์žˆ๊ธฐ ๋•Œ๋ฌธ์— ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150)๋กœ ๋ฉธ๊ท ์ œ๊ฐ€ ์œ ์ž…๋  ์‹œ์— ๋ฌผ๋ฐฉ์šธ ๋˜๋Š” ์•„์ฃผ ์ €์†์œผ๋กœ ์ฑ„์›Œ์ ธ์„œ ์ •๋Ÿ‰ํ™•์ธ์„ผ์„œ(160)๊ฐ€ ์ธ์‹ํ•˜๋ฏ€๋กœ ์˜ค์ฐจ๋ฅผ ์•„์ฃผ ์ •๋ฐ€ํ•˜๊ฒŒ ์ค„ ์ผ ์ˆ˜ ์žˆ๋‹ค. ๊ทธ๋ฆฌ๊ณ , ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150) ํ›„๋‹จ์˜ ๊ฐœํ๋ฐธ๋ธŒ(170)๋ฅผ ๊ฐœ๋ฐฉ์‹œ์ผœ์„œ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”(150) ๋‚ด์˜ ๋ฉธ๊ท ์ œ๋ฅผ ์ €์••์„ ํ˜•์„ฑํ•œ ๊ธฐํ™”๊ธฐ(180)์— ๊ณต๊ธ‰๋˜๋„๋ก ํ•œ๋‹ค.The sterilant metering supply system 100 forms a vacuum in the metering cylinder 150, seals the metering cylinder 150 using the opening / closing valves 140 and 170 before and after the metering cylinder 150, and then the metering cylinder ( 150) by opening the opening and closing valve 140 of the front end to fill the desired amount of the sterilizing agent in the cylinder 150. At this time, because there is a flow control unit 130 between the sterilant container 110 and the metering cylinder 150, when the sterilant is introduced into the metering cylinder 150 is filled with water droplets or very low speed quantitative confirmation sensor 160 Can recognize the error very precisely. Then, the on / off valve 170 at the rear end of the metering cylinder 150 is opened so that the sterilant in the metering cylinder 150 is supplied to the vaporizer 180 having a low pressure.

์ด์™€ ๊ฐ™์ด ์ฒจ๋ถ€๋œ ๋„๋ฉด์„ ์ฐธ์กฐํ•˜์—ฌ ๋ณธ ๋ฐœ๋ช…์„ ์„ค๋ช…ํ•˜์˜€์œผ๋‚˜, ๋ณธ ๋ฐœ๋ช…์˜ ๊ธฐ์ˆ ์  ์‚ฌ์ƒ์„ ๋ฒ—์–ด๋‚˜์ง€ ์•Š๋Š” ๋ฒ”์œ„ ๋‚ด์—์„œ ๋‹ค์–‘ํ•œ ์ˆ˜์ • ๋ฐ ๋ณ€ํ˜•์ด ์ด๋ฃจ์–ด์งˆ ์ˆ˜ ์žˆ์Œ์€ ๋ฌผ๋ก ์ด๋‹ค. ๊ทธ๋Ÿฌ๋ฏ€๋กœ, ๋ณธ ๋ฐœ๋ช…์˜ ๋ฒ”์œ„๋Š” ์„ค๋ช…๋œ ์‹ค์‹œ์˜ˆ์— ๊ตญํ•œ๋˜์–ด ์ •ํ•ด์ ธ์„œ๋Š” ์•ˆ๋˜๋ฉฐ, ํ›„์ˆ ํ•˜๋Š” ํŠนํ—ˆ์ฒญ๊ตฌ๋ฒ”์œ„๋ฟ๋งŒ ์•„๋‹ˆ๋ผ ์ด๋Ÿฌํ•œ ํŠนํ—ˆ์ฒญ๊ตฌ๋ฒ”์œ„์™€ ๊ท ๋“ฑํ•œ ๊ฒƒ๋“ค์— ์˜ํ•ด ์ •ํ•ด์ ธ์•ผ ํ•œ๋‹ค.As described above, the present invention has been described with reference to the accompanying drawings, but various modifications and changes can be made without departing from the spirit of the present invention. Therefore, the scope of the present invention should not be limited to the described embodiments, but should be defined by the claims below and equivalents thereof.

์ƒ๊ธฐํ•œ ๋ฐ”์™€ ๊ฐ™์€ ๋ชฉ์ ์„ ๋‹ฌ์„ฑํ•˜๊ธฐ ์œ„ํ•ด, ๋ณธ ๋ฐœ๋ช…์˜ ์ผ ์ธก๋ฉด์— ๋”ฐ๋ฅด๋ฉด, ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žฅ์ฐฉ๋˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์— ์žˆ์–ด์„œ, ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ฐ€ ์ €์žฅ๋˜๊ณ , ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ์˜ ์ฃผ์ž… ๋ฐ ๋ฐฐ์ถœ์„ ์œ„ํ•œ ์ถœ๊ตฌ๊ฐ€ ๋งˆ๋ จ๋˜๋Š” ์šฉ๊ธฐ; ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๋ฐ€ํ๋œ ์ƒํƒœ๋ฅผ ์œ ์ง€ํ•˜๋„๋ก ์ƒ๊ธฐ ์ถœ๊ตฌ์— ์„ค์น˜๋˜๊ณ , ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žฅ์ฐฉ์‹œ ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ; ๋ฐ ์ƒ๊ธฐ ์šฉ๊ธฐ์— ๋งˆ๋ จ๋˜๊ณ , ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ๊ณผ์••์„ ๋ฐฉ์ง€ํ•˜๊ธฐ ์œ„ํ•œ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์„ ํฌํ•จํ•˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๊ฐ€ ์ œ๊ณต๋œ๋‹ค.In order to achieve the above object, according to an aspect of the present invention, in the sterilant container mounted on the sterilant supply system of the sterilizer, the sterilant is stored, the outlet for the injection and discharge of the sterilant is A container provided; An automatic sealing valve installed at the outlet to maintain the outlet in a closed state and opening the outlet when mounted in the sterilant supply system; And a sterilant container provided in the container and including an overpressure preventing unit for preventing overpressure of the container.

์ƒ๊ธฐ ์šฉ๊ธฐ๋Š”, ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๊ฐ€ ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋„๋ก ์ผ์ธก์— ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์ด ํ˜•์„ฑ๋˜๊ณ , ์ƒ๊ธฐ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ์ƒ๊ธฐ ์ถœ๊ตฌ์ธก์˜ ๋ฐ˜๋Œ€์ธก๊ณผ ์ƒ๊ธฐ ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์˜ ๋‚ด์ธก์— ๊ฐ๊ฐ ๋งˆ๋ จ๋  ์ˆ˜ ์žˆ๋‹ค.The container may be provided with a valve interference prevention groove on one side such that the automatic sealing valve is located inside, and the overpressure prevention unit may be provided on the opposite side of the outlet side and inside the valve interference prevention groove, respectively.

๋ณธ ๋ฐœ๋ช…์˜ ๋‹ค๋ฅธ ์ธก๋ฉด์— ๋”ฐ๋ฅด๋ฉด, ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žˆ์–ด์„œ, ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ฐ€ ์ €์žฅ๋˜๋Š” ์šฉ๊ธฐ์™€, ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ์ถœ๊ตฌ์— ์„ค์น˜๋˜์–ด ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๋ฐ€ํ๋œ ์ƒํƒœ๋ฅผ ์œ ์ง€ํ•˜๋„๋ก ํ•จ๊ณผ ๋ˆ„๋ฆ„์— ์˜ํ•ด ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๋ฅผ ๊ฐ€์ง€๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ; ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ์— ์—ฐ๊ฒฐ๋˜๋„๋ก ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๊ฐ€ ์žฅ์ฐฉ๋˜๊ณ , ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๋ฅผ ๋ˆ„๋ฆ„์— ์˜ํ•ด ๊ฐœ๋ฐฉ์‹œ์ผœ์„œ ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์žฅ์ฐฉ๋ถ€; ์ƒ๊ธฐ ์ถœ๊ตฌ์—์„œ ๋ฐฐ์ถœ๋˜๋Š” ๋ฉธ๊ท ์ œ๋ฅผ ๋ฉธ๊ท ์ฑ”๋ฒ„๋กœ ๊ณต๊ธ‰ํ•˜๊ธฐ ์œ„ํ•œ ๊ฒฝ๋กœ๋ฅผ ์ œ๊ณตํ•˜๋Š” ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์— ์„ค์น˜๋˜๊ณ , ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์กฐ์ ˆํ•˜๋Š” ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›; ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์— ์„ค์น˜๋˜์–ด ๋ฉธ๊ท ์ œ์˜ ๊ณต๊ธ‰์„ ๊ฐœํ์‹œํ‚ค๋Š” ๊ฐœํ๋ฐธ๋ธŒ; ์ƒ๊ธฐ ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›์„ ํ†ต๊ณผํ•˜๋Š” ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์ธก์ •ํ•˜๋Š” ์ •๋Ÿ‰ํ™•์ธ์„ผ์„œ๋ฅผ ํ†ตํ•ด์„œ ๋ฉธ๊ท ์ œ๊ฐ€ ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์„ ํ†ตํ•ด ์ •๋Ÿ‰์œผ๋กœ ๊ณต๊ธ‰๋˜๋„๋ก ํ•˜๋Š” ์ •๋Ÿ‰์‹ค๋ฆฐ๋”; ๋ฐ ์ƒ๊ธฐ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”๋ฅผ ํ†ต๊ณผํ•œ ๋ฉธ๊ท ์ œ๋ฅผ ๊ธฐํ™”์‹œ์ผœ์„œ ์ƒ๊ธฐ ๋ฉธ๊ท ์ฑ”๋ฒ„์— ๊ณต๊ธ‰ํ•˜๋Š” ๊ธฐํ™”๊ธฐ๋ฅผ ํฌํ•จํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์ด ์ œ๊ณต๋œ๋‹ค.According to another aspect of the present invention, in the sterilant supply system of the sterilizer, the container in which the sterilant is stored, and installed in the outlet of the container to maintain the outlet is closed and the outlet is opened by pressing A sterilant container having an automatic sealing valve to enable; A sterilant container mounted to be connected to the automatic sealing valve, and a mounting part for opening the automatic sealing valve by pressing the automatic sealing valve to open the outlet; A flow rate control unit installed in a sterilant supply line providing a path for supplying a sterilant discharged from the outlet to a sterilization chamber, and controlling a flow rate of the sterilant; An on / off valve installed in the sterilant supply line to open and close the supply of the sterilant; A quantitative cylinder through which a sterilant is quantitatively supplied through the sterilant supply line through a quantitative confirmation sensor for measuring a flow rate of the sterilant passing through the flow control unit; And a sterilizer quantitative supply system of a sterilizer including a vaporizer which vaporizes the sterilant passed through the metering cylinder and supplies the sterilant to the sterilization chamber.

์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๋Š”, ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ์ผ์ธก์— ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๊ฐ€ ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋„๋ก ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์ด ํ˜•์„ฑ๋˜๊ณ , ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ๊ณผ์••์„ ๋ฐฉ์ง€ํ•˜๊ธฐ ์œ„ํ•˜์—ฌ ์ƒ๊ธฐ ์šฉ๊ธฐ์— ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ๋งˆ๋ จ๋˜๋ฉฐ, ์ƒ๊ธฐ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ์ƒ๊ธฐ ์ถœ๊ตฌ์ธก์˜ ๋ฐ˜๋Œ€์ธก๊ณผ ์ƒ๊ธฐ ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์˜ ๋‚ด์ธก์— ๊ฐ๊ฐ ๋งˆ๋ จ๋  ์ˆ˜ ์žˆ๋‹ค.The sterilant container, the valve interference prevention groove is formed so that the automatic sealing valve is located on one side of the container, the overpressure preventing unit is provided in the container to prevent the overpressure of the container, the overpressure preventing unit It may be provided on the opposite side of the outlet side and the inside of the valve interference prevention groove, respectively.

์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์—์„œ ์ƒ๊ธฐ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”์˜ ์ „๋‹จ์œผ๋กœ๋ถ€ํ„ฐ ๋ถ„๊ธฐ๋˜๋Š” ๋ถ„๊ธฐ๋ผ์ธ; ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์— ์„ค์น˜๋˜๋Š” ๋ฒคํŠธ๋ฐธ๋ธŒ; ๋ฐ ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์—์„œ ์ƒ๊ธฐ ๋ฒคํŠธ๋ฐธ๋ธŒ์˜ ํ›„๋‹จ์— ์„ค์น˜๋˜๊ณ , ๋ฏธ์ƒ๋ฌผ์ด๋‚˜ ์ด๋ฌผ์งˆ์ด ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์œผ๋กœ ์นจ์ž…ํ•˜๋Š” ์ฐจ๋‹จํ•˜๊ธฐ ์œ„ํ•œ ํ•„ํ„ฐ๋ฅผ ๋” ํฌํ•จํ•  ์ˆ˜ ์žˆ๋‹ค.Branch line branching from the front end of the metering cylinder in the sterilant supply line; A vent valve installed at the branch line; And installed at the rear end of the vent valve in the branch line, and may further include a filter for blocking microorganisms or foreign matter infiltrate into the branch line.

์ƒ๊ธฐ ์žฅ์ฐฉ๋ถ€๊ฐ€ ๋‚ด๋ถ€๊ณต๊ฐ„์— ์„ค์น˜๋˜๊ณ , ์ƒ๊ธฐ ๋‚ด๋ถ€๊ณต๊ฐ„์„ ๊ฐœํ์‹œํ‚ค๊ธฐ ์œ„ํ•œ ๋„์–ด๊ฐ€ ๋งˆ๋ จ๋˜๋Š” ์šฉ๊ธฐ์ฑ”๋ฒ„๋ฅผ ๋” ํฌํ•จํ•  ์ˆ˜ ์žˆ๋‹ค.The mounting unit may further include a container chamber installed in the inner space and provided with a door for opening and closing the inner space.

๋ณธ ๋ฐœ๋ช…์— ๋”ฐ๋ฅธ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰์‹œ์Šคํ…œ์€ ๋ฉธ๊ท  ์žฅ์น˜ ๋“ฑ์— ์ด์šฉ ๊ฐ€๋Šฅํ•˜๋‹ค.The sterilant quantitative supply system according to the present invention can be used for sterilization devices and the like.

10 : ๋ฉธ๊ท ์ฑ”๋ฒ„ 110 : ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ10: sterilization chamber 110: sterilant container

111 : ์šฉ๊ธฐ 112 : ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ111 container 112 automatic sealing valve

113 : ๊ณผ์••๋ฐฉ์ง€์œ ๋‹› 114 : ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ113: overpressure prevention unit 114: valve interference prevention groove

120 : ์žฅ์ฐฉ๋ถ€ 130 : ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›120: mounting portion 130: flow control unit

140,170,190 : ๊ฐœํ๋ฐธ๋ธŒ 150 : ์ •๋Ÿ‰์‹ค๋ฆฐ๋”140, 170, 190: on-off valve 150: fixed quantity cylinder

151 : ๋ฉธ๊ท ์ œ์ฃผ์ž…๊ตฌ 160 : ์ •๋Ÿ‰ํ™•์ธ์„ผ์„œ151: sterilant inlet 160: quantitative confirmation sensor

180 : ๊ธฐํ™”๊ธฐ 210 : ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ180: vaporizer 210: sterilant supply line

220 : ๋ถ„๊ธฐ๋ผ์ธ 230 : ๋ฒคํŠธ๋ฐธ๋ธŒ220: branch line 230: vent valve

240 : ํ•„ํ„ฐ 250 : ์šฉ๊ธฐ์ฑ”๋ฒ„240: filter 250: container chamber

251 : ๋‚ด๋ถ€๊ณต๊ฐ„ 252 : ๋„์–ด251: interior space 252: door

253 : ๋กํ‚น๋ถ€์žฌ253: locking member

Claims (6)

๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žฅ์ฐฉ๋˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ์— ์žˆ์–ด์„œ,A sterilant container mounted on a sterilizer supply system of a sterilizer, ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ฐ€ ์ €์žฅ๋˜๊ณ , ๋ฉธ๊ท ์ œ์˜ ์ฃผ์ž… ๋ฐ ๋ฐฐ์ถœ์„ ์œ„ํ•œ ์ถœ๊ตฌ๊ฐ€ ๋งˆ๋ จ๋˜๋Š” ์šฉ๊ธฐ;A container in which the sterilant is stored and provided with an outlet for injecting and discharging the sterilant; ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๋ฐ€ํ๋œ ์ƒํƒœ๋ฅผ ์œ ์ง€ํ•˜๋„๋ก ์ƒ๊ธฐ ์ถœ๊ตฌ์— ์„ค์น˜๋˜๊ณ , ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žฅ์ฐฉ์‹œ ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ; ๋ฐ An automatic sealing valve installed at the outlet to maintain the outlet in a closed state and opening the outlet when mounted in the sterilant supply system; And ์ƒ๊ธฐ ์šฉ๊ธฐ์— ๋งˆ๋ จ๋˜๊ณ , ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ๊ณผ์••์„ ๋ฐฉ์ง€ํ•˜๊ธฐ ์œ„ํ•œ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์„ ํฌํ•จํ•˜๋Š” ๊ฒƒ์„ ํŠน์ง•์œผ๋กœ ํ•˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ.A sterilant container provided in the container, comprising an overpressure preventing unit for preventing overpressure of the container. ์ œ1ํ•ญ์— ์ž‡์–ด์„œ,In accordance with claim 1, ์ƒ๊ธฐ ์šฉ๊ธฐ๋Š”, ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๊ฐ€ ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋„๋ก ์ผ์ธก์— ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์ด ํ˜•์„ฑ๋˜๊ณ , ์ƒ๊ธฐ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ์ƒ๊ธฐ ์ถœ๊ตฌ์ธก์˜ ๋ฐ˜๋Œ€์ธก๊ณผ ์ƒ๊ธฐ ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์˜ ๋‚ด์ธก์— ๊ฐ๊ฐ ๋งˆ๋ จ๋˜๋Š” ๊ฒƒ์„ ํŠน์ง•์œผ๋กœ ํ•˜๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ.The vessel is sterilized, characterized in that the valve interference prevention groove is formed on one side so that the automatic sealing valve is located inside, and the overpressure prevention unit is provided on the opposite side of the outlet side and inside the valve interference prevention groove, respectively. My container. ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ์— ์žˆ์–ด์„œ, In the sterilant supply system of the sterilizer, ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ฐ€ ์ €์žฅ๋˜๋Š” ์šฉ๊ธฐ์™€, ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ์ถœ๊ตฌ์— ์„ค์น˜๋˜์–ด ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๋ฐ€ํ๋œ ์ƒํƒœ๋ฅผ ์œ ์ง€ํ•˜๋„๋ก ํ•จ๊ณผ ๋ˆ„๋ฆ„์— ์˜ํ•ด ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๋ฅผ ๊ฐ€์ง€๋Š” ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ;A sterilant container having a container in which the sterilant is stored and an automatic sealing valve installed at an outlet of the container to maintain the outlet in a closed state and to open the outlet by pressing; ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ์— ์—ฐ๊ฒฐ๋˜๋„๋ก ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๊ฐ€ ์žฅ์ฐฉ๋˜๊ณ , ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๋ฅผ ๋ˆ„๋ฆ„์— ์˜ํ•ด ๊ฐœ๋ฐฉ์‹œ์ผœ์„œ ์ƒ๊ธฐ ์ถœ๊ตฌ๊ฐ€ ๊ฐœ๋ฐฉ๋˜๋„๋ก ํ•˜๋Š” ์žฅ์ฐฉ๋ถ€;A sterilant container mounted to be connected to the automatic sealing valve, and a mounting part for opening the automatic sealing valve by pressing the automatic sealing valve to open the outlet; ์ƒ๊ธฐ ์ถœ๊ตฌ์—์„œ ๋ฐฐ์ถœ๋˜๋Š” ๋ฉธ๊ท ์ œ๋ฅผ ๋ฉธ๊ท ์ฑ”๋ฒ„๋กœ ๊ณต๊ธ‰ํ•˜๊ธฐ ์œ„ํ•œ ๊ฒฝ๋กœ๋ฅผ ์ œ๊ณตํ•˜๋Š” ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์— ์„ค์น˜๋˜๊ณ , ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์กฐ์ ˆํ•˜๋Š” ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›;A flow rate control unit installed in a sterilant supply line providing a path for supplying a sterilant discharged from the outlet to a sterilization chamber, and controlling a flow rate of the sterilant; ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์— ์„ค์น˜๋˜์–ด ๋ฉธ๊ท ์ œ์˜ ๊ณต๊ธ‰์„ ๊ฐœํ์‹œํ‚ค๋Š” ๊ฐœํ๋ฐธ๋ธŒ;An on / off valve installed in the sterilant supply line to open and close the supply of the sterilant; ์ƒ๊ธฐ ์œ ๋Ÿ‰์กฐ์ ˆ์œ ๋‹›์„ ํ†ต๊ณผํ•˜๋Š” ๋ฉธ๊ท ์ œ์˜ ์œ ๋Ÿ‰์„ ์ธก์ •ํ•˜๋Š” ์ •๋Ÿ‰ํ™•์ธ์„ผ์„œ๋ฅผ ํ†ตํ•ด์„œ ๋ฉธ๊ท ์ œ๊ฐ€ ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์„ ํ†ตํ•ด ์ •๋Ÿ‰์œผ๋กœ ๊ณต๊ธ‰๋˜๋„๋ก ํ•˜๋Š” ์ •๋Ÿ‰์‹ค๋ฆฐ๋”; ๋ฐA quantitative cylinder through which a sterilant is quantitatively supplied through the sterilant supply line through a quantitative confirmation sensor for measuring a flow rate of the sterilant passing through the flow control unit; And ์ƒ๊ธฐ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”๋ฅผ ํ†ต๊ณผํ•œ ๋ฉธ๊ท ์ œ๋ฅผ ๊ธฐํ™”์‹œ์ผœ์„œ ์ƒ๊ธฐ ๋ฉธ๊ท ์ฑ”๋ฒ„์— ๊ณต๊ธ‰ํ•˜๋Š” ๊ธฐํ™”๊ธฐ๋ฅผ ํฌํ•จํ•˜๋Š” ๊ฒƒ์„ ํŠน์ง•์œผ๋กœ ํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ.A sterilant quantitative supply system of a sterilizer, characterized in that it comprises a vaporizer to vaporize the sterilant passed through the metering cylinder to the sterilization chamber. ์ œ3ํ•ญ์— ์žˆ์–ด์„œ, The method of claim 3, ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ ์šฉ๊ธฐ๋Š”, ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ์ผ์ธก์— ์ƒ๊ธฐ ์ž๋™๋ฐ€ํ๋ฐธ๋ธŒ๊ฐ€ ๋‚ด์ธก์— ์œ„์น˜ํ•˜๋„๋ก ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์ด ํ˜•์„ฑ๋˜๊ณ , ์ƒ๊ธฐ ์šฉ๊ธฐ์˜ ๊ณผ์••์„ ๋ฐฉ์ง€ํ•˜๊ธฐ ์œ„ํ•˜์—ฌ ์ƒ๊ธฐ ์šฉ๊ธฐ์— ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ๋งˆ๋ จ๋˜๋ฉฐ, ์ƒ๊ธฐ ๊ณผ์••๋ฐฉ์ง€์œ ๋‹›์ด ์ƒ๊ธฐ ์ถœ๊ตฌ์ธก์˜ ๋ฐ˜๋Œ€์ธก๊ณผ ์ƒ๊ธฐ ๋ฐธ๋ธŒ๊ฐ„์„ญ๋ฐฉ์ง€ํ™ˆ์˜ ๋‚ด์ธก์— ๊ฐ๊ฐ ๋งˆ๋ จ๋˜๋Š” ๊ฒƒ์„ ํŠน์ง•์œผ๋กœ ํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ.The sterilant container, the valve interference prevention groove is formed so that the automatic sealing valve is located on one side of the container, the overpressure preventing unit is provided in the container to prevent the overpressure of the container, the overpressure preventing unit Sterilizer quantitative supply system of the sterilizer, characterized in that provided on the opposite side of the outlet side and the inside of the valve interference prevention groove, respectively. ์ œ 3 ํ•ญ์— ์žˆ์–ด์„œ, The method of claim 3, wherein ์ƒ๊ธฐ ๋ฉธ๊ท ์ œ๊ณต๊ธ‰๋ผ์ธ์—์„œ ์ƒ๊ธฐ ์ •๋Ÿ‰์‹ค๋ฆฐ๋”์˜ ์ „๋‹จ์œผ๋กœ๋ถ€ํ„ฐ ๋ถ„๊ธฐ๋˜๋Š” ๋ถ„๊ธฐ๋ผ์ธ;Branch line branching from the front end of the metering cylinder in the sterilant supply line; ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์— ์„ค์น˜๋˜๋Š” ๋ฒคํŠธ๋ฐธ๋ธŒ; ๋ฐA vent valve installed at the branch line; And ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์—์„œ ์ƒ๊ธฐ ๋ฒคํŠธ๋ฐธ๋ธŒ์˜ ํ›„๋‹จ์— ์„ค์น˜๋˜๊ณ , ๋ฏธ์ƒ๋ฌผ์ด๋‚˜ ์ด๋ฌผ์งˆ์ด ์ƒ๊ธฐ ๋ถ„๊ธฐ๋ผ์ธ์œผ๋กœ ์นจ์ž…ํ•˜๋Š” ์ฐจ๋‹จํ•˜๊ธฐ ์œ„ํ•œ ํ•„ํ„ฐ๋ฅผ ๋” ํฌํ•จํ•˜๋Š” ๊ฒƒ์„ ํŠน์ง•์œผ๋กœ ํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ.A sterilant quantitative supply system of a sterilizer, characterized in that it is installed at the rear end of the vent valve in the branch line, and further comprises a filter for blocking microorganisms or foreign substances from entering the branch line. ์ œ 3 ํ•ญ์— ์žˆ์–ด์„œ,The method of claim 3, wherein ์ƒ๊ธฐ ์žฅ์ฐฉ๋ถ€๊ฐ€ ๋‚ด๋ถ€๊ณต๊ฐ„์— ์„ค์น˜๋˜๊ณ , ์ƒ๊ธฐ ๋‚ด๋ถ€๊ณต๊ฐ„์„ ๊ฐœํ์‹œํ‚ค๊ธฐ ์œ„ํ•œ ๋„์–ด๊ฐ€ ๋งˆ๋ จ๋˜๋Š” ์šฉ๊ธฐ์ฑ”๋ฒ„๋ฅผ ๋” ํฌํ•จํ•˜๋Š” ๊ฒƒ์„ ํŠน์ง•์œผ๋กœ ํ•˜๋Š” ๋ฉธ๊ท ๊ธฐ์˜ ๋ฉธ๊ท ์ œ ์ •๋Ÿ‰ ๊ณต๊ธ‰ ์‹œ์Šคํ…œ.The mounting unit is installed in the inner space, the sterilant quantitative supply system of the sterilizer, characterized in that further comprising a container chamber provided with a door for opening and closing the inner space.
PCT/KR2012/006050 2011-08-04 2012-07-30 Sterilant container and system for supplying fixed amount of sterilant of sterilizer using same Ceased WO2013019044A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1020110077931A KR101112506B1 (en) 2011-08-04 2011-08-04 Sterilizer container and sterilizer quantitative supply system using the sterilizer
KR10-2011-0077931 2011-08-04

Publications (2)

Publication Number Publication Date
WO2013019044A2 true WO2013019044A2 (en) 2013-02-07
WO2013019044A3 WO2013019044A3 (en) 2013-04-04

Family

ID=45840201

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2012/006050 Ceased WO2013019044A2 (en) 2011-08-04 2012-07-30 Sterilant container and system for supplying fixed amount of sterilant of sterilizer using same

Country Status (2)

Country Link
KR (1) KR101112506B1 (en)
WO (1) WO2013019044A2 (en)

Families Citing this family (4)

* Cited by examiner, โ€  Cited by third party
Publication number Priority date Publication date Assignee Title
KR101254190B1 (en) * 2012-09-26 2013-04-18 (์ฃผ) ๋ฐ”์ด๋ฉ”์Šค Apparatus for evaporationing sterilant in low temperature plasma sterilizer
KR101675059B1 (en) 2016-04-27 2016-11-10 ์„œ์ •๊ถŒ apparatus for supplying fixed amount of sterilant of sterilant device
KR101969086B1 (en) 2018-08-22 2019-08-13 ์ฃผ์‹ํšŒ์‚ฌ ๋กœ์šฐํ…œ Vessel for chemicals
KR102630266B1 (en) * 2023-05-25 2024-01-29 ์ฃผ์‹ํšŒ์‚ฌ ํ”Œ๋ผ์ฆˆ๋งต Sterilizer Storage Device and Sterilization Device Comprising the Same

Family Cites Families (6)

* Cited by examiner, โ€  Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05270559A (en) * 1992-03-27 1993-10-19 Hoyu Co Ltd Container
JP3493366B2 (en) * 1993-06-14 2004-02-03 ๆ—ฅๆœฌใƒขใƒณใ‚ตใƒณใƒˆๆ ชๅผไผš็คพ Connection structure of cartridge type chemical liquid container used for chemical liquid sprayer
JPH08133362A (en) * 1994-11-02 1996-05-28 Shiseido Co Ltd Aerosol container with burst-preventive mechanism
US6279622B1 (en) 2000-02-07 2001-08-28 Ethicon, Inc. Method and system for delivering and metering liquid sterilant
JP4829133B2 (en) * 2007-01-19 2011-12-07 ใ‚จใ‚ขใƒปใ‚ฆใ‚ฉใƒผใ‚ฟใƒผๆ ชๅผไผš็คพ Sterilizer
KR100845533B1 (en) * 2007-02-23 2008-07-10 ์ฃผ์‹ํšŒ์‚ฌ ํœด๋จผ๋ฉ”๋””ํ… Liquid dosing device of plasma sterilization system

Also Published As

Publication number Publication date
WO2013019044A3 (en) 2013-04-04
KR101112506B1 (en) 2012-02-24

Similar Documents

Publication Publication Date Title
AU2009270318B2 (en) A container with a frangible sealed access and a vapour permeable vent
ES2366598T3 (en) PROCEDURE AND DISTRIBUTION SYSTEM AND DOSAGE OF LIQUID STERILIZATION SUBSTANCES.
CA2808717C (en) Hydrogen peroxide metering unit
CN108473215B (en) Apparatus and method for protecting and deprotecting fluid paths in controlled environment enclosures
WO2013019044A2 (en) Sterilant container and system for supplying fixed amount of sterilant of sterilizer using same
EP1542735B1 (en) A pre-sterilisation chamber for a processing enclosure
BR112020007170A2 (en) method and apparatus for sterilizing endoscopes
US8715264B2 (en) Charged hydrator
BR102017025406A2 (en) independent vacuum chamber sterilization system
EP2379120A2 (en) Sterile liquid transfer port
CA2226248C (en) Containment and delivery apparatus for hazardous fluids
JP7296569B2 (en) Sample storage device
KR101198618B1 (en) Pathogenic waste disposal case
EP1493450B1 (en) Sterilization vacuum chamber door closure
KR200297888Y1 (en) A multiple sterilizer
US20250235610A1 (en) Filling apparatus and method for filling a reusable reservoir of a medical dispensing device
US5891390A (en) Method for reducing the danger of fire or explosion from sterilant leakage
WO2026013775A1 (en) Washing/disinfecting device and chemical bottle
KR20070047037A (en) Syringe device
MXPA97001896A (en) Containment and assortment apparatus for fluid danger
MXPA02009134A (en) Apparatus for safely containing and delivering hazardous fluid substances from at least two supply cylinders.
BR122013010297B1 (en) METHOD FOR STERILIZING AN ITEM IN A SEALABLE STERILIZATION CHAMBER

Legal Events

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

Ref document number: 12819291

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: DE

32PN Ep: public notification in the ep bulletin as address of the adressee cannot be established

Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 112(1) EPC (EPO FOM 1205A DD 11/06/14)

122 Ep: pct application non-entry in european phase

Ref document number: 12819291

Country of ref document: EP

Kind code of ref document: A2