WO2003000167A1 - Method for processing easy-to-reduce resin molded article for infectious medical practice and its apparautus - Google Patents

Method for processing easy-to-reduce resin molded article for infectious medical practice and its apparautus Download PDF

Info

Publication number
WO2003000167A1
WO2003000167A1 PCT/JP2002/006140 JP0206140W WO03000167A1 WO 2003000167 A1 WO2003000167 A1 WO 2003000167A1 JP 0206140 W JP0206140 W JP 0206140W WO 03000167 A1 WO03000167 A1 WO 03000167A1
Authority
WO
WIPO (PCT)
Prior art keywords
volume
medical waste
waste
volume reduction
water
Prior art date
Application number
PCT/JP2002/006140
Other languages
French (fr)
Japanese (ja)
Inventor
Kenichi Hino
Original Assignee
Kuraray 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
Priority claimed from JP2001192246A external-priority patent/JP2003002918A/en
Priority claimed from JP2001270232A external-priority patent/JP2003073498A/en
Priority claimed from JP2002142272A external-priority patent/JP2003325593A/en
Application filed by Kuraray Co., Ltd. filed Critical Kuraray Co., Ltd.
Publication of WO2003000167A1 publication Critical patent/WO2003000167A1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B17/00Recovery of plastics or other constituents of waste material containing plastics
    • B29B17/0026Recovery of plastics or other constituents of waste material containing plastics by agglomeration or compacting
    • B29B17/0047Compacting complete waste articles
    • 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
    • A61L11/00Methods specially adapted for refuse
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B09DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
    • B09BDISPOSAL OF SOLID WASTE
    • B09B3/00Destroying solid waste or transforming solid waste into something useful or harmless
    • B09B3/0075Disposal of medical waste
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B17/00Recovery of plastics or other constituents of waste material containing plastics
    • B29B17/0026Recovery of plastics or other constituents of waste material containing plastics by agglomeration or compacting
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B17/00Recovery of plastics or other constituents of waste material containing plastics
    • B29B17/04Disintegrating plastics, e.g. by milling
    • B29B2017/0424Specific disintegrating techniques; devices therefor
    • B29B2017/0476Cutting or tearing members, e.g. spiked or toothed cylinders or intermeshing rollers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/753Medical equipment; Accessories therefor
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/52Mechanical processing of waste for the recovery of materials, e.g. crushing, shredding, separation or disassembly
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/62Plastics recycling; Rubber recycling

Definitions

  • the present invention is intended to reduce the volume of infectious medical waste that has been contaminated or possibly contaminated with infectious pathogens, infectious body fluids, etc. at medical institutions, etc. This method is intended to reduce the amount of waste containers used and the number of collections by waste disposal companies, and to improve the efficiency of infectious medical waste disposal systems.
  • This method is intended to reduce the amount of waste containers used and the number of collections by waste disposal companies, and to improve the efficiency of infectious medical waste disposal systems.
  • infectious waste is stored in a polyethylene bag separate from other garbage, placed in a sturdy cardboard box, and commissioned to be incinerated by a disposal company licensed by a public agency. I have.
  • Japanese Patent Application Laid-Open No. HEI 5-344500 discloses a method for producing linoleic and quinol using polyvinyl alcohol fibers that are water-soluble only at a temperature exceeding 50 ° C.
  • a method has been proposed in which gowns, gowns and other articles are manufactured, dissolved in high-temperature water, and disposed of as sewage.
  • this method not only increases the environmental burden due to the flow of wastewater containing high concentrations of organic matter, but also reduces infectious waste without sterilizing infectious microorganisms and inactivating hepatitis viruses and prions. It will be dumped in sewage, creating major environmental and sanitary problems.
  • the present inventor has recognized that incineration and high-temperature pyrolysis are more appropriate for disposal of infectious medical waste than dumping it into the sewer, investigated.
  • both parties are required to treat any type of infectious waste as a treatment target, and to sterilize infectious pathogens for the purpose of turning infectious waste into general waste or landfilling it as it is.
  • this required heating to around 200 ° C and a specification to apply a pressure of several tens of tons, leading to an increase in the size and cost of the equipment.
  • Hei 7-26553365 describes a polyethylene having an open top for storing medical waste and a valve for removing air inside the container.
  • a “medical waste container” consisting of plastic bags has been proposed. According to the present invention, waste is put into a container from a slit at the top of the container, the slit is sealed with an adhesive tape, and the air inside the container is evacuated with a syringe needle from a rubber ball-like valve provided on the container. The purpose is to reduce the volume by compressing the container by the atmospheric pressure, and to save the space for storing waste and the transportation cost.
  • Japanese Patent Application Laid-Open No. 5-32301 contains waste and contains it in waste before it is put into an incinerator.
  • a garbage bin ⁇ garbage bag which is at least partially made of a porous film, has been proposed, which is a “waste container” that can release the generated water in a vapor state.
  • Japanese Patent Application Laid-Open No. 5-32301 is intended for general garbage, the idea of actively reducing the volume of waste, and droplets containing infectious pathogens contained in waste. There was no idea to increase the safety by filtering the water.
  • the present invention aims to spread the volume of infectious waste to small and medium-sized hospitals nationwide, and to reduce the volume of waste safely using compact and inexpensive equipment. It is an object of the present invention to provide a medical material, a bag therefor, and a method for reducing the volume of waste using the device. Disclosure of the invention
  • the present invention provides an infectious medical waste (A) mainly composed of a resin molded product made of a hydrophilic resin that is melted by hot water or steam at 50 ° C. or higher in the presence of water (B).
  • A infectious medical waste
  • B This is a method for reducing the volume of infectious medical waste, which is characterized by treating at a temperature of 70 to 150 ° C.
  • a bag for storing the infectious medical waste (A) and the water (B) of the present invention which is made of a thermoplastic film, wherein a pathogen filtering means can be attached to or detached from a side surface or an opening of the bag body.
  • This is a method for reducing the volume of infectious medical waste, characterized in that it is stored in a storage bag provided in a non-removable state.
  • the infectious medical waste of the present invention is characterized in that the hydrophilic resin that melts by hot water or water vapor at 50 ° C or higher is a fibrous product or a resin molded product made of a polyvinyl alcohol-based resin. It is a method of treating sexual medical waste.
  • hot water or water vapor at 50 ° C or higher which is the main infectious medical waste of the present invention, is used.
  • This is a method for treating infectious medical waste in which the hydrophilic resin melted by air is a polyvinyl alcohol homopolymer or an ethylene-vinyl alcohol copolymer having an ethylene copolymerization ratio of 1 to 24 mol%.
  • thermoplastic film constituting the storage bag for reducing the volume of infectious medical waste of the present invention is formed of a film made of a thermoplastic polymer having a heat resistant temperature of 100 ° C. or higher. It is a method of processing objects.
  • a check valve is provided in the filtering means attached to the side surface or the opening of the storage bag body for reducing volume of infectious medical waste of the present invention, and the storage bag for volume reduction is infected with the check bag.
  • the present invention treats medical waste consisting of a hydrophilic resin that is melted with hot water or steam at 50 ° C. or higher at a temperature of 70 ° C. to 150 ° C., and treats the infectious medical waste (A ),
  • a housing provided with an electromagnetic wave absorption function or an electromagnetic wave shielding function to prevent the emission of electromagnetic waves generated from the infectious medical waste volume reduction device, and a housing inside the device.
  • Infectious medicine comprising a heating unit consisting of a heating chamber, which may have a rotating or vibrating heating pot, which is detachably mounted, a heating means which is a microwave, and a means for controlling the supply of heat. It is a volume reduction device for waste.
  • FIG. 1 and FIG. 2 are schematic views showing an example of a storage bag used to reduce the volume of infectious medical waste of the present invention.
  • FIG. 3 is an example of a volume reduction device of the present invention, which is a horizontal device.
  • FIG. 4 shows an example of a volume reduction device according to the present invention, which is a vertical device.
  • FIG. 5 is an example of a volume reduction device of the present invention, which is a horizontal device.
  • FIG. 6 shows an example of an extruder-type apparatus, which is an example of the volume reducing apparatus of the present invention.
  • FIG. 7 shows an example of a volume reduction device of the present invention, which is a rotary drum type device.
  • FIG. 8 shows an example of the volume reducing device of the present invention, which is a device with a shredder type shredder.
  • FIG. 9 shows an example of the volume reducing device of the present invention, which is a device for melting in a hopper.
  • the target medical product made of a hydrophilic resin functions as a container or a fiber product under ordinary use conditions such as body temperature.
  • the space occupied by the wastes is reduced and the apparent volume is reduced by expelling air inside the medical products and between the products.
  • the hydrophilic resin is heated by adding water as a plasticizer, its melting temperature will be lower than usual and it will melt at a very low temperature, or it will become a solution with high concentration and high viscosity. It utilizes the phenomenon of resilience.
  • hydrophilic resin constituting a medical product that satisfies these conditions, it is practically insoluble in water at 50 ° C or lower, but has a water content of 5% or more (20 ° C, humidity 65%). % Moisture absorption under the same conditions) .
  • Homopolymers or copolymers of polyvinyl alcohol are particularly preferred, and when a copolymer of polyvinyl alcohol is used, melt spinning is preferred.
  • Polyvinyl alcohol-based resin is also excellent in this respect because it is a halogen-free resin and does not generate harmful substances typified by dioxin when incinerated.
  • This resin is mainly used as a resin molded product or a fiber product.
  • the shape is not particularly limited, and the structure may be porous or non-porous. Is also good.
  • Medical volume-decreasing tree of the present invention The shape of the fat molding is used, for example, for placing trays and cups used to place tissue and waste removed from patients, scalpels with blood, iron, tweezers, and other devices.
  • Containers and instruments such as trays, bags and boxes, face guards, disposable tweezers and forceps, urinalysis cups used for medical examinations, sample tubes and petri dishes, incubators, etc. Examples include tableware and the like used by patients who are isolated due to infectious diseases, and molded articles such as utensils such as tubes and sheets having a non-porous structure, especially bulky compared to the weight. It may be a large molded product.
  • a fiber obtained by a usual spinning method is further converted into a woven fabric, a knitted fabric or a nonwoven fabric, or a nonwoven fabric is formed directly from a resin by a method such as a spunbond method or flash spinning.
  • a fiber product obtained by melting an ethylene-vinyl alcohol copolymer to form a nonwoven fabric at the same time as melt spinning is suitable for the present invention because it has moderate hydrophilicity and is inexpensive.
  • the fiber diameter ⁇ fiber length of the fibrous material can be arbitrarily selected according to the intended use of the molded product.
  • textile products include evening ol, curtains, sleepwear, headcovers, masks, bandages, tapes, underpats, and other materials that may be contaminated with body fluids of patients who may have contracted an infectious disease.
  • Examples include diapers, sheets, gauze, absorbent cotton, napkins, tissue paper, wipers, etc., which may be contaminated during surgery, such as surgical gowns, drapes, sheets, patient clothing, aprons, gauze, absorbent cotton, etc.
  • an operating table and a wiping cloth for wiping blood around the operating table are exemplified, and all textile products discarded in single use are included in the textile products according to the present invention.
  • such a fiber product may be a product obtained by mixing or laminating fibers made of a resin other than the hydrophilic resin by cotton mixing, cross-knitting or the like in order to improve comfort and other performances.
  • the waste to be reduced in volume includes various textile products for medical use, Garbage with infectious bodily fluids generated by inspection and food inspection institutions, waste containing infectious pathogens such as zoonotic diseases such as zoonotic diseases that occur in animal hospitals and animal breeding facilities, and nursing care facilities Of unsanitary waste and sanitary pests (mite, etc.), medical garbage generated in home care homes, and pathogenic Legionella and Salmonella bacteria that appear safe in household goods.
  • infectious pathogens such as zoonotic diseases such as zoonotic diseases that occur in animal hospitals and animal breeding facilities
  • medical garbage generated in home care homes include pathogenic Legionella and Salmonella bacteria that appear safe in household goods.
  • those that can be reduced in volume without destroying them those that do not contain dangerous substances such as piercing bags, but other unpleasant garbage that emits an unpleasant odor like diapers Is also included.
  • the operation of adding water may be, for example, simply wetting with water at room temperature in the case of textiles.
  • the water used for this purpose may be simple tap water, it may be sewage mixed with patient's blood, urine or other contaminants, or water used for cleaning the floor around the operating table may be made of textile. May be used, or water containing a disinfectant to sterilize pathogenic bacteria may be used.
  • a gel layer is formed only on the surface of the fiber product mass in contact with the hot water, and this gel layer is applied to the inside of the fiber mass of the hot water.
  • the efficiency of volume reduction may be reduced because it prevents intrusion. Therefore, it is preferred that the water be added to the textile using cold water so that the water is distributed as evenly as possible throughout the textile.
  • the medical volume-reducing resin molded product of the present invention may be used, for example, when a tissue collected from a patient is placed on a tray-like container, blood permeates to contaminate articles other than the container, Also, if blood adheres to surgical gowns or sheets, it must not penetrate the blood.
  • a substantially water-impermeable layer on the surface or inside of the medical volume-reducible resin molded product.
  • the resin molded product is made of two or more nonwoven fabrics and / or textiles. In the case of textile products formed by laminating fabrics, water resistance is provided by providing a water-impermeable layer on the surface or inside, or by treating the laminated nonwoven layer with a water repellent.
  • the water-impermeable layer provided in the medical volume-reducible resin molded article of the present invention may have a property of allowing water vapor to permeate but not allowing water droplets to permeate.
  • the material constituting such a water-impermeable layer may be a non-woven fabric of polyolefin, but the resin is not deformed by water at body temperature and is shrunk or dissolved by hot water or high-temperature steam.
  • Such resins include trans polyisoprene having a softening point in the range of 50 to 100 ° C., ethylene-vinyl acetate copolymer, polyproprolactone resin and plasticizer.
  • a film made of a polyvinyl alcohol resin is preferably used as the water-soluble resin.
  • water repellent examples include a fluorine-based water- and oil-repellent, an ethylene urea-based, a melamine-based, a methylolamide-based, and a silicon-based, and an arbitrary one is selected from these.
  • the amount of water contained in the textile should be such that it wets the textile evenly but does not drip from the textile.
  • the mass ratio of infectious medical waste Z water is It is preferably in the range of 70 Z30 to 20 Z80, and more preferably in the range of 67/33 to 25 Z75. If the amount of water used is too large, the weight of the waste will be too heavy, and the shape of the waste taken out after volume reduction will not be solid, making it difficult to handle, and will require a large amount of energy when incinerated later. Required. Conversely, if the amount of water used is too small, parts that are not wet with water will be conspicuous, and the volume reduction rate of waste will be insufficient.
  • the total amount of newly added water be within the above range in consideration of the contained water.
  • 70 ° C. or higher is employed, and preferably 9 ° C. or more. 0 ° C or more, more preferably 100 ° C or more, but if the temperature is higher than 150 ° C, the running cost required to generate a high temperature increases, and water vaporization increases.
  • the resulting volume expansion is rapid and remarkable, which may make it difficult to control the operation of the apparatus, which is not preferable.
  • it is 140 ° C. or lower.
  • the infectious medical waste of the present invention is stored in a storage bag and can be reduced in volume by the above method.
  • the storage bag body used in the present invention needs to be made of a thermoplastic film, and is preferably made of a heat-resistant thermoplastic film that can withstand the temperature reached by the heating means of the present invention.
  • the thermoplastic polymer from which such a bag can be produced is preferably a thermoplastic polymer having a heat resistance temperature of 100 ° C. or more, more preferably 105 ° C. or more.
  • Examples of such a material include polyolefin, and among them, high-density polyethylene, medium-density polyethylene, and polypropylene are preferable, and low-cost bag materials other than polyolefin include polyethylene terephthalate (PET) and polybutylene terephthalate. Examples thereof include polyesters such as sauce and polymethylene terephthalate.
  • Low-density polyethylene has low heat resistance of 90 ° C or less, and is suitable as a storage bag for reducing the volume of infectious medical waste of the present invention.
  • the heat-resistant temperature referred to in the present invention is ASTMD 759 test The values measured according to the law are shown.
  • a bag for reducing the volume of infectious medical waste of the present invention is formed from a film produced from these materials by an inflation molding method or a biaxial stretching method. Can be produced. If these materials are too hard to seal tightly when tying the mouth of the bag, it may be possible to use a plywood or other laminated material to reduce this.
  • a pathogen filtering means is provided on the side surface or the opening of the storage bag main body, and the filtering means is a filter material which does not allow infectious bodily fluids to pass through. It can remove blood that contains pathogens in the form of fine droplets and scattered, and may be one that performs filtration by adsorption instead of physical filtration. Blood contains a large number of white blood cells and red blood cells with a diameter of about 10 m, and blood droplets are thought to aggregate with these blood cell components as nuclei.Therefore, filtration means that can remove dust with a diameter of 10 m or less can be removed.
  • the finest mist particles among water droplets have a diameter of 1 xm or more.
  • filtration means that can remove more than 99% of particles with a diameter of 1 / are used. More preferred.
  • HEP II filter ULPA filter
  • electret filter The shape of the filtering means is not particularly limited, but is preferably cylindrical or sheet-like from the viewpoint of ease of attachment to the bag.
  • a material for the filtration means is a nonwoven fabric.
  • a nonwoven fabric can be manufactured by various manufacturing methods such as a wet method, a card method, a spunbond method, a melt blown method, and a flash spinning method.
  • Nonwoven fabrics made of fiber by melt blown or flash spinning methods have a number of uniform micropores and are preferred in terms of air permeability and bacterial barrier properties.Electret-treated fabrics are particularly preferred. .
  • the filter member is preferably made of a water-repellent polymer such as polypropylene or polyester, or a water-repellent material, since even if water droplets adhere to the surface, the filter member is not clogged.
  • the non-woven fabric used as a material for the film is one layer and reinforced For other purposes, two or more layers may be laminated with another nonwoven fabric, paper, reinforcing sheet, or the like.
  • a deodorizing material may be used in combination with the filtering means.
  • those which adsorb, absorb or react with fecal odor, putrefaction odor, and chemical odor are preferably used.
  • Such materials include activated carbon, non-woven fabrics and sponges made of ion-exchange resin, non-volatile or high-boiling basic substances, acidic substances, plant extracts, and substances that can react with thiols.
  • a nonwoven fabric or sponge impregnated with one or more agents can be used.
  • Deodorants include cunic acid, malic acid, vitamin C and other acidic substances, sodium carbonate, polyethyleneimine, hexamethylenetetramine, other basic substances, alum water, hydrous glyoxal, and other substances that can react with thiols , Copper pin mouth finnulin sodium, champignon extract, catechin, polyphenol, persimmon extract, other plant extracts, cyclodextrin, amphoteric surfactant, abietic acid salts and the like. It is even more preferable that the above-mentioned filter also has deodorizing performance.
  • the inside of the storage bag can be reduced in pressure, but it is preferable to attach a check valve to the filtering means so that outside air does not enter the storage bag in the reduced pressure
  • a check valve for example, a flat plastic or rubber piece closes a hole on a flat plate, a curved surface closes a hole provided on a curved surface like a ball valve, or a side of a pipe like a check valve on a bicycle tube. Any type can be used, such as a type in which a resilient force bar closes a hole formed in a hole.
  • the filter may be an irreversible valve of a type in which the resin member is in contact with the filtering means and the filter is clogged by dissolving the resin member after the internal air is released.
  • This check valve is also preferably made of an organic substance such as plastic or rubber and does not leave ash after incineration, and is preferably simple so as to be supplied at the lowest possible cost.
  • the filtering means can be used by attaching it to the mouth of the storage bag.
  • heat bonding such as a heat sealing method is preferable, but using a commercially available adhesive, a double-sided tape, a hot-melt film, or other adhesive material. Is also good.
  • the hot melt film include polyvinyl acetate, polyamide, and ethylene-vinyl acetate copolymer.
  • a means for sealing the mouth of the storage bag for example, when a filler made of a laminate such as a nonwoven fabric is previously attached to the bag by thermal bonding or the like, the mouth of the bag is tied directly, A preferred method is to wind the mouth tightly with a string, rubber string, rubber band, or adhesive vinyl tape and seal it. If a filter, deodorizing means, or check valve is attached to the cylinder to form a single unit (filtering means) and the bag is connected to the mouth of a regular bag, the mouth of the bag should be in the center of the pursed bag.
  • Fig. 1 shows an example of a bag for waste that can release the gas in the bag through a filter.
  • A is a bag equipped with the filter means (3) and the check valve (4) of the present invention.
  • B is a detailed view of the filter (3) and the check valve (4), and C is an external view of the bag after putting waste into a bag and sealing it.
  • Fig. 2 also shows an example of a storage bag used to reduce the volume of infectious medical waste.
  • D is a front view of the storage bag
  • E is a filter consisting of a filter (3) and a check valve (4).
  • F shows the filter unit of E (filtration means) in the opening of the storage bag after waste is put in the storage bag of D. ) Put on the bag FIG.
  • One application of this method of facilitating the transport of infectious medical waste is to reduce the volume by using only the aforementioned hydrophilic resin. It is also recommended to wrap up infectious waste that is not hydrophilic to reduce its volume. That is, the volume of the hydrophilic resin molded article may be reduced in a state where various infectious wastes generated in the operating room, such as ordinary plastic containers, syringes, and gloves, are mixed with the hydrophilic resin molded article. .
  • the hydrophilic resin molded product accounts for at least 20%, preferably 33 to 99% of the total mass of infectious medical waste, and the water contained in the hydrophilic resin product relative to the hydrophilic resin. Of the hydrophilic resin at a temperature of 70 to 150 ° C.
  • the entire medical waste can be fixed as one block.
  • This method involves reducing the volume due to the volume reduction of the hydrophilic resin molded product itself and, for example, filling the inside of the syringe or sample tube with water vapor, creating a vacuum when it cools down, and dissolving wet heat there.
  • the infectious medical waste referred to in the present invention includes not only medical waste contaminated with infectious substances but also medical waste possibly contaminated with infectious substances. .
  • the apparent volume of infectious medical waste, especially medical fiber waste, is greatly reduced by the volume reduction process, but if water is ideally distributed, it will be reduced regardless of the bulk density before volume reduction.
  • the specific gravity of the treated waste is about 1.1 to 1.2, and the volume reduction rate is high. Even so, the strength depends on the bulkiness of the fiber waste when it is thrown into a waste container. It is a very compact one-half or less, and the very bulky one is about 20.
  • volume reducing device for infectious medical waste suitable for carrying out the method of the present invention (hereinafter referred to as a volume reducing device) will be described with reference to the drawings.
  • the volume reduction device of the present invention comprises a housing (1), a heating chamber (2), a heating means (3), and a heat source to be sent to the heating means.
  • Means for controlling the supply and specifically for controlling the supply of power.
  • microwaves are used as the heating means in this volume reduction device, but if a microphone mouth wave is used, the electromagnetic waves are shielded or absorbed in order to prevent radiation of the electromagnetic waves generated from this volume reduction device. It is preferable to provide the function of By shielding or absorbing the electromagnetic waves, medical devices installed around the volume reduction device can be prevented from being erroneously operated.
  • the case is made of a metal plate with good conductivity, or if the case is not made of metal plate, the main part of the case is made of metal mesh.
  • the grounding is performed by welding or plating metal, the use of conductive plastics containing conductive fibers such as metal or carbon or conductive powder, or the use of ferrite.
  • a paint containing a substance that absorbs electromagnetic waves There is a method such as using a paint containing a substance that absorbs electromagnetic waves, and one or some of these techniques are used in combination.
  • the volume reduction device may be covered with another conductive case or conductive sheet for further perfection.
  • the volume reduction device of the present invention needs to have a heating chamber (2), and a lid (5) that forms the heating chamber is attached to the housing together with the housing so as to be openable and closable.
  • the housing (1) is provided with a microswitch for detecting the opening of the lid and shutting off the power in order to avoid various dangers such as burns of the workers.
  • a heating pot (4) may be detachably mounted or fixed in the heating chamber.
  • the heating pot (4) can be covered with a polyethylene or polypropylene heat-resistant bag (6) that can withstand the volume reduction temperature to prevent contamination of the heating pot (4). If it becomes dirty, the heating pot can be removed from the heating chamber and cleaned and disinfected.
  • this heating pot can be connected to a means for rotating or vibrating it, and by applying kinetic energy to the waste heat in the wet heat state, the air can be accelerated to escape, and hooks and kinetics can be used. The air may be expelled by stirring or poking.
  • water that is added to the waste and condensed in the heating chamber and water that is added for heating and condensed in the heating chamber are added to the heating chamber.
  • Drainage outlets and drainage pipes may be provided to deal with pooling phenomena and to drain sewage when cleaning and disinfecting the heating chamber.
  • a means for connecting to a vacuum line, a cock, or the like may be provided in the exhaust pipe (9) so that the heating chamber can be operated under a reduced pressure condition.
  • the volume reducing device of the present invention requires a heating means.
  • the heating means include a microphone opening wave, steam, a heating wire, and infrared rays.
  • microwaves can increase the temperature of the waste in the shortest time, and may be one that reduces the volume while using sterilization with a preferable force steam.
  • the heating means used in FIGS. 3 to 5 is a microwave, and the microwave (10) generated by the microwave generator (3) is provided in the heating pot (4) in the heating chamber (2). The waste and water (1 2) put in the tank will be heated.
  • reference numeral 16 denotes an adsorption chamber for adsorbing an unusual odor generated by the volume reduction treatment.
  • the volume reduction device K of the present invention requires a detection means for detecting the state of the resin, Examples of such detection means include an infrared or contact temperature detector (13), or an optical, contact, or ultrasonic level detector (14).
  • the former temperature detector is used to confirm that the heating means is operating normally and to supply appropriate power to the heating means. The purpose of this is to prevent the temperature from rising too high and leading to a fire.
  • the latter level detector is a liquid level detector to prevent the resin in the wet heat molten state during volume reduction operation from expanding excessively due to the vapor pressure of water and contaminating the inside of the heating chamber. When a certain level of expansion is detected, the power supply to the heating means is limited or stopped.
  • the means for controlling the power supply has a temperature adjustment function and a timer function, but has a function to shut down or limit the power supply to the heating means based on the abnormal signals from the various detection means described above. Things. Further, it may have a function of detecting a failure in the heating means or overheating in the heating chamber and issuing an alarm, or a signal indicating that one cycle of volume reduction has been completed.
  • the heating pot is placed on a turntable (15) so as to be uniformly heated.
  • waste and water (1 2) are fed into a heating section (2 2) from a charging hopper (2 1) and heated by a screw ⁇ . It may be a device that heats and melts waste while moving it inside the section and removes it from the heating section. Also, as shown in Fig. 7, the drum (23) containing waste is rotated in the heating chamber (2), and water vapor heated by the heat source (24) passes from below through the drum wall. It may be a device that plasticizes and reduces the volume of waste. In these figures, 25 is water and 26 is a controller. In the apparatus shown in FIG. 6, the heating section (2 2) is covered, so that the heating section can be regarded as a housing (1).
  • the volume reducing device used in the present invention is put into the hopper (2 1), and fed to the shredder type cutting machine (3 1) by the roller pair (3 7) under the hopper to be cut, and the cut material is heated in the lower heating chamber (2).
  • the entire device including the cutting machine is a casing (1), and the heating element (33) can control the power supply so that the temperature inside the heating pot can be adjusted. ing.
  • the apparatus shown in FIG. 9 is also an example of the apparatus of the present invention. That is, in the apparatus shown in Fig. 9, the waste (1 2) is put into the hopper (2 1), steam (32) is blown into the hopper (2 1), and water is added as necessary. This is a device that dissolves waste as a viscous liquid in pairs (37), drops it down, and receives it in the lower container.
  • (34) is a water tank
  • (35) is a steam generator
  • (36) is a waste level sensor.
  • the hopper controls the supply of steam and the hopper temperature by controlling the supply of electric power by controlling the power supply with the hopper as the heating section, the hopper and the roller pair and the lower receiver as the housing, the heating means as the steam, and the steam generator as the power supply. It is a system to adjust. Also, a structure that optically detects whether or not waste is present in the hopper and controls the rotation of the roller and the on / off of steam may be employed. Also in these devices, since the heating section is covered, it can be considered that the heating section exists in the housing.
  • the volume-reduced waste is a viscous liquid at a high temperature, but becomes a solid having almost no fluidity when cooled to room temperature.
  • Solids referred to in the present invention are those that have no fluidity at room temperature, and that, when placed in a container at room temperature, do not instantaneously flow out of the container even if the container is knocked down. And so-called high-viscosity conditions), and is therefore extremely easy to handle.
  • the volume reduction treatment of the medical volume-reducible resin molded product of the present invention generates infectious medical waste. It is generally performed at a medical site, but it may be performed in an operating room, a corridor of a hospital room, a hospital entrance, a vacant lot outside the hospital, etc., a little further away from the site, and further suboptimally. As a countermeasure, the waste may be transported after performing volume reduction processing in the collection vehicle so that a large amount of waste can be loaded and transported on the collection vehicle. After performing this volume reduction treatment, the medical waste is incinerated or pyrolyzed into gas using a special incineration facility that can be incinerated particularly at high temperatures.
  • volume reduction test of the volume-reducible medical resin molded product in the present invention was performed by the following method.
  • V D volume reduction test
  • Example 1 Using the same nonwoven fabric as in Example 1, the hot water conditions were set to the amounts and temperatures shown in Table 1, and a volume reduction test was performed. Table 1 shows the results.
  • Example 1 A volume reduction test was performed under the same hot water conditions as in Example 1 except that the same polyvinyl alcohol resin as in Example 1 was used as a raw material, and the basis weight of the nonwoven fabric was changed to that shown in Table 1. Table 1 shows the results.
  • Example 2 In place of the nonwoven fabric made of the polyvinyl alcohol resin of Example 1, a spun-pound nonwoven fabric having a basis weight of 30 g / m 2 made of a polypropylene resin was used. ⁇ A volume reduction test was performed under the same hot water conditions as in Example 1. . Table 1 shows the results. Hot water was not absorbed into the nonwoven fabric at all, and no change in volume was observed. Comparative Example 2
  • a volume reduction test was performed using the same nonwoven fabric as in Comparative Example 1 with the amount and temperature of hot water shown in Table 1. Table 1 shows the results. As in Comparative Example 1, no change in volume was shown.
  • Example 8 The same non-woven fabric as in Example 1 was hand-made into a square cloth of the same mass (200 g) as the surgical gown, which was rolled unfolded and made of 45 L high-density polyethylene for infectious waste. When I put it in my bag, it was filled with nine pieces. Steam is evenly blown into this bag to absorb the steam into the non-woven fabric. When the total mass increases by 1300 g, stop blowing the steam and press the foot many times to squeeze and release the air. However, the non-woven fabric in the bag shrank to about 5 L. The resulting mass is placed in a 500 W microwave oven [ER-240 (W), manufactured by Toshiba Corporation], and irradiated with microwaves for 30 seconds to expand the rice cake so that the rice cake expands. The volume was reduced to 4 liters when removed from the microwave and stomp again to deflate. (The temperature in the microwave during heating was in the range of 90 to 110 ° C.) Example 8
  • a tray having a length of 10 cm, a width of 20 cm, a depth of 2 cm, and a thickness of 1.5 mm was prepared.
  • the apparent volume occupied by this box was 400 cm 3 .
  • This tray was used as a container for scalpels, scissors, etc. used in the surgery during surgery.
  • Example 9 The tray after use was filled with water for 5 minutes, softened in the same microwave oven as in Example 7 for 20 seconds, and sandwiched between two thick plates and subjected to a load of 60 kg. 0 cm 3 to shrink ivy (temperature in the microwave oven during heating was in the range of 9 0 ⁇ 1 1 0 ° C).
  • Ethylene 5 mole% copolymerized with dissolution temperature 8 0, water content 9.1% ethylene one vinyl alcohol copolymer made of basis weight 35 of GZm 2 nonwoven 8 0 ° polyvinyl alcohol C dissolved [(strain ) manufactured by Kuraray Co. PVA-1 1 7, sheet of water content 10.6% made film basis weight 6 was laminated O gZm 2 - DOO width 1 0 0 cm, the sheets were cut to a length 2 0 0 cm Produced.
  • a bag for infectious waste consisting of high-density polyethylene with a maximum capacity of 20 liters with a maximum capacity of 20 liters and a width of 405 mm x width 660 mm and thickness of 30 m as shown in Fig. Produced.
  • a cylindrical tube made of high-density polyethylene with an inner diameter of 13 mm and a length of 6 cm was melt blown with polypropylene, and the average fiber diameter was 3 m.
  • basis weight is processed mass per unit area of a laminated Sea Bok was a 1 0 g Roh m 2 and the paper making method 1 0 g / m 2 nonwoven and wood pulp, the gas in the bag area of 5 cm 2 to the outside Equipped with a filter for release, absorbent cotton impregnated with malic acid in the cylinder, and hydrated darioxal
  • a cotton wool impregnated with the rubber was packed in, and a check valve consisting of a polypropylene pedestal and a rubber piece was attached to the other end by hot melt bonding to produce a filter unit as shown in FIG.
  • the bag expanded significantly, but steam gushed out from the outlet of the filter unit and the bag did not burst.
  • the sample was taken out, and the temperature was measured immediately using a thermocouple (Digital Thermometer CT-700S, Custorn) to show 90. From this and the state of the contents at the time of irradiation, the internal temperature of the kettle had reached the range of 90 to 110 ° C.
  • the volume of the sheet after removal was reduced to 33 OmL, and the volume was reduced to 1 Z5 compared to before the microwave treatment.
  • Example 10 As in Example 10 (1), put three disposable diapers and 0.7 kg of water from a cardiology ward into a 20-L high-density polyethylene bag without folding it, and attach a membrane filter. Without the same microscopy as in Example 9. When the waves were irradiated, the contents inside the bag expanded violently, and a large amount of water vapor was released from the outlet of the cylinder without a filter, and some of the droplets of the contents adhered to the inner wall of the heating pot.
  • the bag was compressed by atmospheric pressure to reduce the volume as in Example 10. Then, the sterilized gauze with the inner wall of the heating pot wet with sterile water was brought into contact with soybean, casein, digest, and agar medium, and this medium was stored in an incubator at 35 for 3 days and visually observed. However, when a large number of colonies were observed on the agar medium, and they were observed under a microscope, rod-shaped E. coli having a short diameter of 1.1 to 1.1 and a long diameter of 2.0 to 6.0 m and a diameter of 1 zm were observed on the agar medium. Numerous spherical Staphylococcus aureus were observed. Industrial applicability
  • the volume reduction method and apparatus of the present invention greatly reduce the melting temperature of the hydrophilic resin by utilizing the plasticizing effect of water, so that the volume is reduced as compared to melting a conventional thermoplastic resin as it is. Since the temperature required for the treatment is low, the operation can be performed with a small amount of power using a simple device, and a significant cost reduction can be achieved in both initial costs and running costs.
  • the use of the storage bag of the present invention during volume reduction processing does not require dangerous work such as taking out infectious waste out of the bag or opening the bag and doing something. Anybody can safely and easily reduce the volume of waste anywhere, and the waste after volume reduction has been disinfected, further improving work safety.
  • the present invention can be used as long as a specific hydrophilic resin molded product is used. Volume can be reduced without eliminating infectious waste It is possible to greatly reduce container costs, transportation costs, and the like related to the processing of refuse.

Abstract

The method for processing infectious medical waste according to the invention is a method for reducing the volume of infectious medical waste characterized in that infectious medical waste (A) mainly composed of hydrophilic resin molded articles fused by hot water or steam of above 50 °C is processed at 70 °C to 150 °C in the presence of water (B). The volume reducing apparatus for infectious medical waste is an apparatus for reducing the volume of infectious medical waste (A) by processing at 70 °C to 150 °C medical waste composed of hydrophilic resin fusible by hot water or steam of above 50ºC comprises a casing, a heating unit, and means for controlling heating means and supply of heat.

Description

明細 : 感染性医療用易減容性樹脂成形物の処理方法及びそのための装置 技術分野 Description : Method for treating infectious medical easily-reducible resin molded product and apparatus therefor
本発明は、 医療機関等において、 感染性病原体、 感染性体液等で汚染 された、 あるいは汚染された可能性のある等の事由により発生した感染 性医療廃棄物を減容化することにより、 廃棄物容器の使用量の低減と廃 棄物処理業者の収集回数の低減を図り、 感染性医療廃棄物の廃棄システ ムの効率向上を図る方法であり、 更に減容化するのに適した装置に関す る。 背景技術  The present invention is intended to reduce the volume of infectious medical waste that has been contaminated or possibly contaminated with infectious pathogens, infectious body fluids, etc. at medical institutions, etc. This method is intended to reduce the amount of waste containers used and the number of collections by waste disposal companies, and to improve the efficiency of infectious medical waste disposal systems. About. Background art
病院などの医療機関においては、 伝染病の原因となる感染性病原体、 肝炎や エイズ等のウィルスを含む感染性体液等により器具や衣服等が汚染される可能 性のある作業がつきものである。 このような作業に使用された各種物品は、 消 毒および滅菌の処置が厳密に施された後に再使用されたり、 あるいは感染性廃 棄物として焼却処分されている。 このうち、 感染性廃棄物は、 他のゴミとは別 のポリエチレン製の袋に貯め、 その袋を頑丈な段ボール箱に入れて、 公的機関 の許可を得た処理業者に焼却を委託されている。 このような感染性廃棄物の大 きな部分を血液で汚染されたプラスチック製品や、 手術着、 シーツ等の非常に 嵩張る物品が占めているが、 これらの感染性医療廃棄物、 特に繊維製品は重量 ベースで見ると僅かな量であるにも関わらず、 体積ベースで見ると非常に大き な量を占めている。 従って、 感染性廃棄物を収容するポリエチレン袋や、 袋を 保護するための段ボールの使用量は非常に多く、 廃棄物を一旦保管しておくた めに特別の広いスペースが必要であったり、 廃棄物を収集運搬する自動車が病 院を巡回する回数も不必要に多かった。 すなわち、 従来の廃棄物処理システム は、 それ自身が利益を生まないものにかける行為にしては非常に効率が悪く、 高いコストを要するものであった。 In hospitals and other medical institutions, there are tasks that may cause contamination of equipment and clothing by infectious agents that cause infectious diseases, infectious bodily fluids containing viruses such as hepatitis and AIDS, and the like. The various items used in such operations have been rigorously disinfected and sterilized and then reused or incinerated as infectious waste. Of these, infectious waste is stored in a polyethylene bag separate from other garbage, placed in a sturdy cardboard box, and commissioned to be incinerated by a disposal company licensed by a public agency. I have. A large portion of such infectious waste is made up of plastic products contaminated with blood, very bulky items such as surgical gowns and sheets, but these infectious medical wastes, especially textiles, Despite the small amount on a weight basis, it accounts for a very large amount on a volume basis. Therefore, the amount of polyethylene bags used to store infectious waste and cardboard to protect the bags is extremely large, requiring extra large space to temporarily store the waste, or waste. A car that collects and transports sickness The number of visits to the hospital was unnecessarily large. In other words, conventional waste treatment systems are very inefficient and costly to use for those that do not generate profits.
この問題を解決する方法として、日本特開平 5— 3 4 5 0 1 3号には、 5 0 °C を越える温度でのみ水溶性であるポリビニルアルコール製の繊維を用いてリネ ン類、 夕オル、 ガウンその他の物品を作製し、 これを高温の水に溶解して下水 として廃棄する方法が提案されている。 しかしながら、 この方法では、 高濃度 の有機物を含む排水を流すため環境負荷を増大させるのみならず、 感染性微生 物の滅菌や肝炎ウィルスやプリオン等の不活化が確認されないまま感染性廃棄 物が下水に投棄されることになり、 環境上、 衛生上大きな問題を発生させるこ とになる。 さらに進んだ方法として、 感染性廃棄物を加熱溶融してブロック状 の塊に減容化する装置、 廃棄物を粉砕して減容化する装置等が提案、 市販され ている。 しかし、 このような市販の装置は非常に大型で高価であり、 それを運 転するために要する電気代も高く、 全国の病院や医療機関に広く普及させるた めには経済的な問題が大きいものであった。  As a method for solving this problem, Japanese Patent Application Laid-Open No. HEI 5-344500 discloses a method for producing linoleic and quinol using polyvinyl alcohol fibers that are water-soluble only at a temperature exceeding 50 ° C. A method has been proposed in which gowns, gowns and other articles are manufactured, dissolved in high-temperature water, and disposed of as sewage. However, this method not only increases the environmental burden due to the flow of wastewater containing high concentrations of organic matter, but also reduces infectious waste without sterilizing infectious microorganisms and inactivating hepatitis viruses and prions. It will be dumped in sewage, creating major environmental and sanitary problems. As more advanced methods, devices that reduce the volume of infectious waste by heating and melting it into block-like lumps and devices that reduce the volume of waste by crushing the waste have been proposed and marketed. However, such commercially available devices are very large and expensive, and the electricity required to operate them is expensive, and there is a significant economic problem in spreading them widely to hospitals and medical institutions nationwide. Was something.
本発明者は感染性医療廃棄物の処分には、 下水道への投棄よりも焼却処分や 高温熱分解の方が適切であるとの認識のもとに、 廃棄物の加熱溶融装置と粉砕 装置について検討した。 その結果、 両者とも処理対象として感染性廃棄物の種 類を問わず処理することと、 感染性廃棄物を一般廃棄物としたりそのまま埋め 立てたりする事を目的として感染性病原体を滅菌することを前提としており、 それがために 2 0 0 °C前後への加熱や数十トンもの圧力を加える仕様を必要と し、 装置の大きさと価格の増大を招いていることが判った。  The present inventor has recognized that incineration and high-temperature pyrolysis are more appropriate for disposal of infectious medical waste than dumping it into the sewer, investigated. As a result, both parties are required to treat any type of infectious waste as a treatment target, and to sterilize infectious pathogens for the purpose of turning infectious waste into general waste or landfilling it as it is. As a prerequisite, it was found that this required heating to around 200 ° C and a specification to apply a pressure of several tens of tons, leading to an increase in the size and cost of the equipment.
一方、 上記したような、 大型装置を要する大量処理型の対策とは異なり、 廃 棄物の発生現場でできる対策として廃棄物の減容化のみを考えた廃棄物用の袋 に関する提案がある。 これは廃棄物の袋の内部を減圧にして、 大気圧により袋 を外から圧迫して廃棄物を減容化するものであり、 どこでも誰でも安価に簡単 に廃棄物の減容化を図ることができる点で画期的な方法である。 この方法は、 繊維製品や軟質容器のように圧迫により容易に変形してみかけの体積を減ずる 物のみに対象が限定されるが、 前述したように、 医療現場におけるこのような 廃棄物は体積べ一スでは全体の廃棄物の中で非常に大きな量を占めており、 そ の効果は非常に大きい。 減容化を図るための方法として日本特開平 7— 2 6 5 3 6 5号では、 医療廃棄物を収容するための開放頂部と、 容器内部の空気を除 去するためのバルブを備えたポリエチレン製の袋からなる 「医療廃棄物容器」 が提案されている。 この発明は容器の上部のスリツ卜から廃棄物を容器に入れ、 スリツトを粘着テープで密閉し、 容器に設けられたゴムボールのへソのような バルブより注射針を用いて内部の空気を抜き取り、 大気圧により容器を圧迫し て減容化するものであり、 これによる廃棄物の保管スペースの節約と運送コス 卜の節約を目的とするものである。 また感染性廃棄物の減容化に関するもので はないが、 日本特開平 5— 3 2 3 0 1号には廃棄物が収納され、 焼却炉に投入 されるまでの間に廃棄物中に含有される水分を蒸気の状態で放出することが可 能な 「廃棄物収容体」 なる、 少なくとも一部が多孔質フィルムからなるゴミ箱 ゃゴミ袋が提案されている。 On the other hand, unlike the large-volume treatment measures that require large equipment as described above, there is a proposal for a waste bag that considers only volume reduction of waste as a measure that can be taken at the site where waste is generated. This is to reduce the volume of waste by reducing the pressure inside the waste bag and compressing the bag from the outside with atmospheric pressure. This is a revolutionary method in that the volume of waste can be reduced. This method is limited to those that easily deform by compression to reduce the apparent volume, such as textiles and flexible containers. At one time, it accounts for a very large amount of the total waste, and the effect is very large. As a method for reducing the volume, Japanese Patent Application Laid-Open No. Hei 7-26553365 describes a polyethylene having an open top for storing medical waste and a valve for removing air inside the container. A “medical waste container” consisting of plastic bags has been proposed. According to the present invention, waste is put into a container from a slit at the top of the container, the slit is sealed with an adhesive tape, and the air inside the container is evacuated with a syringe needle from a rubber ball-like valve provided on the container. The purpose is to reduce the volume by compressing the container by the atmospheric pressure, and to save the space for storing waste and the transportation cost. Although it is not related to volume reduction of infectious waste, Japanese Patent Application Laid-Open No. 5-32301 contains waste and contains it in waste before it is put into an incinerator. A garbage bin ゃ garbage bag, which is at least partially made of a porous film, has been proposed, which is a “waste container” that can release the generated water in a vapor state.
しかし、 日本特開平 7— 2 6 5 3 6 5号は、  However, Japanese Unexamined Patent Publication No.
①廃棄物どうしの隙間に介在する空気を除去して減容化するのであるが、 廃棄 物そのものを他の状態に変えてしまうものではないため、 最密充填率の壁を越 えて大幅な減容化を達成することは無理であり減容化の程度が限られる、 (1) The volume of waste is removed by removing the air present in the gaps between the wastes. However, since the waste itself is not changed to another state, it greatly decreases beyond the wall of the closest packing ratio. It is impossible to achieve volume reduction and the degree of volume reduction is limited,
②減容化後も廃棄物の感染性は維持されており、 作業の危険性は高いままであ る、 (2) Even after the volume reduction, the infectivity of the waste is maintained and the danger of work remains high.
③容器の中の空気の除去に注射器を使用する等、 非常に手間がかかるし、 感染 性廃棄物の取扱いにおいては廃棄物の袋の中の空気を追い出す作業は病原体が 付着した飛沫を撒き散らす可能性があるため禁忌とされ、 廃棄物の袋を圧迫し ない事が原則とされている、 ④袋を減圧にした際に、 袋の内部に混在する注射針やメスの替刃等の尖った物 が袋の表面に押し付けられて袋から露出した際には、 感染性を有する内容物に より感染事故を起こす可能性が否定できない、 (3) It takes a lot of time, such as using a syringe to remove air from the container. In handling infectious waste, the task of expelling the air from the waste bag disperses droplets with pathogens attached. It is contraindicated because of the possibility that waste bags should not be squeezed in principle. し た When the bag is evacuated and a sharp object such as a syringe needle or a scalpel blade that is mixed inside the bag is pressed against the surface of the bag and exposed from the bag, it may cause infectious contents. I cannot deny the possibility of causing more infection accidents,
等の問題があり、 減容化の程度、 操作性と安全性の点で改善の余地を残すもの であった。 However, there was room for improvement in terms of volume reduction, operability and safety.
また、 日本特開平 5— 3 2 3 0 1号は一般のゴミを対象にするものであり、 廃棄物を積極的に減容化する思想、 廃棄物中に含まれる感染性病原体を含む飛 沫を濾過して安全性を高めるような思想はなかった。  Also, Japanese Patent Application Laid-Open No. 5-32301 is intended for general garbage, the idea of actively reducing the volume of waste, and droplets containing infectious pathogens contained in waste. There was no idea to increase the safety by filtering the water.
従って、 本発明は、 全国津々浦々の中小病院に至るまで感染性廃棄物の減容 化を広く普及させるため、 コンパクトで安価な装置を用いて安全に廃棄物の減 容化を行うための、 特定の医療用材料と、 そのための袋と、 装置を用いた廃棄 物の減容化方法を提供することを目的とする。 発明の開示  Therefore, the present invention aims to spread the volume of infectious waste to small and medium-sized hospitals nationwide, and to reduce the volume of waste safely using compact and inexpensive equipment. It is an object of the present invention to provide a medical material, a bag therefor, and a method for reducing the volume of waste using the device. Disclosure of the invention
すなわち、 本発明は、 5 0 °C以上の熱水又は水蒸気により溶融する親水性樹 脂からなる樹脂成形物を主体とする感染性医療廃棄物 (A) を水 (B ) の存在 下において、 7 0〜 1 5 0 °Cの温度で処理することを特徴とする感染性医療廃 棄物の減容化方法である。  That is, the present invention provides an infectious medical waste (A) mainly composed of a resin molded product made of a hydrophilic resin that is melted by hot water or steam at 50 ° C. or higher in the presence of water (B). This is a method for reducing the volume of infectious medical waste, which is characterized by treating at a temperature of 70 to 150 ° C.
そして、 本発明の感染性医療廃棄物 (A) と水 (B ) とを、 熱可塑性フィル ムからなる収納袋であって、 該袋本体の側面又は開口部に病原菌濾過手段が着 脱可能又は着脱不能の状態で備えられている収納袋に収納することを特徴とす る感染性医療廃棄物の減容化方法である。  A bag for storing the infectious medical waste (A) and the water (B) of the present invention, which is made of a thermoplastic film, wherein a pathogen filtering means can be attached to or detached from a side surface or an opening of the bag body. This is a method for reducing the volume of infectious medical waste, characterized in that it is stored in a storage bag provided in a non-removable state.
さらに、 本発明の感染性医療廃棄物の主体となる 5 0 °C以上の熱水又は水蒸 気により溶融する親水性樹脂が、 ポリビニルアルコール系樹脂からなる繊維製 品または樹脂成形品である感染性医療廃棄物の処理方法である。  Furthermore, the infectious medical waste of the present invention is characterized in that the hydrophilic resin that melts by hot water or water vapor at 50 ° C or higher is a fibrous product or a resin molded product made of a polyvinyl alcohol-based resin. It is a method of treating sexual medical waste.
さらに、 本発明の感染性医療廃棄物の主体となる 5 0 °C以上の熱水又は水蒸 気により溶融する親水性樹脂がポリビニルアルコールホモポリマー、 あるいは エチレン共重合割合 1〜 2 4モル%のエチレン—ビニルアルコール共重合体で ある感染性医療廃棄物の処理方法である。 Furthermore, hot water or water vapor at 50 ° C or higher, which is the main infectious medical waste of the present invention, is used. This is a method for treating infectious medical waste in which the hydrophilic resin melted by air is a polyvinyl alcohol homopolymer or an ethylene-vinyl alcohol copolymer having an ethylene copolymerization ratio of 1 to 24 mol%.
そして、 本発明の感染性医療廃棄物の減容化用収納袋を構成する熱可塑性フ イルムが耐熱温度が 1 0 0 °C以上の熱可塑性ポリマーからなるフィルムにより 形成されている感染性医療廃棄物の処理方法である。  The infectious medical waste in which the thermoplastic film constituting the storage bag for reducing the volume of infectious medical waste of the present invention is formed of a film made of a thermoplastic polymer having a heat resistant temperature of 100 ° C. or higher. It is a method of processing objects.
さらに、 本発明の感染性医療廃棄物の減容化用収納袋本体の側面又は開口部 に装着されている濾過手段に逆止弁が備えられており、 そして該減容化用収納 袋に感染性医療廃棄物を入れた後、 袋の中を減圧する感染性医療廃棄物の処理 方法である。  Further, a check valve is provided in the filtering means attached to the side surface or the opening of the storage bag body for reducing volume of infectious medical waste of the present invention, and the storage bag for volume reduction is infected with the check bag. This is a method of treating infectious medical waste in which the pressure inside the bag is reduced after putting the infectious medical waste.
そして、 本発明は 5 0 °C以上の熱水又は水蒸気により溶融する親水性樹脂か らなる医療廃棄物を 7 0〜 1 5 0 °Cの温度で処理して該感染性医療廃棄物(A) を減容化させるための装置であって、 感染性医療廃棄物用減容装置から発生す る電磁波の放散を防ぐための電磁波吸収機能あるいは電磁波遮蔽機能を付与し た筐体と、 内部に着脱自在に載置された、 回転あるいは振動する加熱釜を有し ていてもよい加熱室からなる加熱部と、 マイクロウエーブである加熱手段と、 熱の供給を制御する手段とからなる感染性医療廃棄物用減容装置である。 図面の簡単な説明  Then, the present invention treats medical waste consisting of a hydrophilic resin that is melted with hot water or steam at 50 ° C. or higher at a temperature of 70 ° C. to 150 ° C., and treats the infectious medical waste (A ), A housing provided with an electromagnetic wave absorption function or an electromagnetic wave shielding function to prevent the emission of electromagnetic waves generated from the infectious medical waste volume reduction device, and a housing inside the device. Infectious medicine comprising a heating unit consisting of a heating chamber, which may have a rotating or vibrating heating pot, which is detachably mounted, a heating means which is a microwave, and a means for controlling the supply of heat. It is a volume reduction device for waste. BRIEF DESCRIPTION OF THE FIGURES
第 1図および第 2図は本発明の感染性医療廃棄物を減容化するために 用いる収納袋の一例を示す概略図である。  FIG. 1 and FIG. 2 are schematic views showing an example of a storage bag used to reduce the volume of infectious medical waste of the present invention.
第 3図は本発明の減容化装置の一例で、 横型の装置である。  FIG. 3 is an example of a volume reduction device of the present invention, which is a horizontal device.
第 4図は本発明の減容化装置の一例で、 縦型の装置である。  FIG. 4 shows an example of a volume reduction device according to the present invention, which is a vertical device.
第 5図は本発明の減容化装置の一例で、 横型の装置である。  FIG. 5 is an example of a volume reduction device of the present invention, which is a horizontal device.
第 6図は本発明の減容化装置の一例で、 押出機タイプの装置である。 第 7図は本発明の減容化装置の一例で、 回転ドラム型の装置である。 第 8図は本発明の減容化装置の一例で、 シュレッダータイプの細断機 付きの装置である。 FIG. 6 shows an example of an extruder-type apparatus, which is an example of the volume reducing apparatus of the present invention. FIG. 7 shows an example of a volume reduction device of the present invention, which is a rotary drum type device. FIG. 8 shows an example of the volume reducing device of the present invention, which is a device with a shredder type shredder.
第 9図は本発明の減容化装置の一例で、 ホッパー内で溶融させる装置 である。 発明を実施するための最良の形態  FIG. 9 shows an example of the volume reducing device of the present invention, which is a device for melting in a hopper. BEST MODE FOR CARRYING OUT THE INVENTION
本発明の感染性医療廃棄物の減容化により運搬を容易にする方法において、 対象とする親水性樹脂製の医療用製品は、 体温程度の通常の使用条件において は容器や繊維製品としての機能を普通に発揮し、 それを廃棄する時になって、 該医療用製品の内部や製品の間に介在する空気を追い出すことによって廃棄物 が占める空間が減少し見かけの体積が減少するものである。 この操作は、 親水 性樹脂に可塑剤となる水を含ませて加熱すると、 通常よりもその溶融温度が下 がって非常に低い温度で溶融したり、 あるいは高濃度 ·高粘度の溶液になった りする現象を利用している。 このような条件を満たす医療用製品を構成する親 水性樹脂としては、 5 0 °C以下の水には実質的に溶解しないが、 5 %以上の水 分率 (2 0 °C、 湿度 6 5 %の条件での吸湿率) を有する親水性の合成樹脂が挙 げられ、 特にポリビニルアルコールのホモポリマ一またはコポリマ一が好まし く、 ポリビニルアルコールのコポリマーを使用する場合には、 好ましくは溶融 紡糸が可能で、 安価に使い捨ての繊維製品が得られることからエチレン含有量 :!〜 2 4モル%、 さらに好ましくはエチレン含有量 3〜 1 4モル%のエチレン 一ビニルアルコール共重合体が挙げられる。 ポリビニルアルコール系樹脂は、 ノンハロゲン系樹脂であることから焼却処分の際に、 ダイォキシンで代表され る有害物質を発生しないため、 この点からも優れている。  In the method for facilitating transportation by reducing the volume of infectious medical waste according to the present invention, the target medical product made of a hydrophilic resin functions as a container or a fiber product under ordinary use conditions such as body temperature. When disposing of the medical products, the space occupied by the wastes is reduced and the apparent volume is reduced by expelling air inside the medical products and between the products. In this operation, if the hydrophilic resin is heated by adding water as a plasticizer, its melting temperature will be lower than usual and it will melt at a very low temperature, or it will become a solution with high concentration and high viscosity. It utilizes the phenomenon of resilience. As a hydrophilic resin constituting a medical product that satisfies these conditions, it is practically insoluble in water at 50 ° C or lower, but has a water content of 5% or more (20 ° C, humidity 65%). % Moisture absorption under the same conditions) .Homopolymers or copolymers of polyvinyl alcohol are particularly preferred, and when a copolymer of polyvinyl alcohol is used, melt spinning is preferred. An ethylene-vinyl alcohol copolymer having an ethylene content of! To 24 mol%, more preferably an ethylene content of 3 to 14 mol%, is preferable because a disposable fiber product can be obtained at a low cost. Polyvinyl alcohol-based resin is also excellent in this respect because it is a halogen-free resin and does not generate harmful substances typified by dioxin when incinerated.
この樹脂は主として樹脂成形品あるいは繊維製品として使用され、 樹脂成形 品として使用される場合、 形状については特に制限はなく、 またその構造は多 孔質であっても、 あるいは非多孔質であってもよい。 本発明の医療用減容性樹 脂成形物の形状としては、 例えば、 患者から取り出した組織や汚物を載置する ために使用するトレーやカップ、 血液の付着したメス、 鉄、 ピンセット等の器 具を載置するために使用するトレー、 それらの器具等を消毒する場所まで運搬 するに収容する袋および箱、 フェースガード、 ディスポのピンセットや鉗子、 医療検査に用いられる検尿カップ、 サンプル管やシャーレ、 培養器等の容器や 器具類、 伝染病のため隔離されている患者が使用する食器類等が例示され、 さ らに非多孔質の構造を有するチューブやシート等の器具類等の成形品、 特に重 量と比べて嵩が大きい成形品であってもよい。 This resin is mainly used as a resin molded product or a fiber product. When used as a resin molded product, the shape is not particularly limited, and the structure may be porous or non-porous. Is also good. Medical volume-decreasing tree of the present invention The shape of the fat molding is used, for example, for placing trays and cups used to place tissue and waste removed from patients, scalpels with blood, iron, tweezers, and other devices. Containers and instruments such as trays, bags and boxes, face guards, disposable tweezers and forceps, urinalysis cups used for medical examinations, sample tubes and petri dishes, incubators, etc. Examples include tableware and the like used by patients who are isolated due to infectious diseases, and molded articles such as utensils such as tubes and sheets having a non-porous structure, especially bulky compared to the weight. It may be a large molded product.
繊維製品として使用される場合は、 例えば、 通常の紡糸法により得られた繊 維をさらに織物、 編物または不織布としたもの、 またはスパンボンド法ゃフラ ッシュ紡糸などの方法により樹脂から直接不織布としたものが好ましく使用で きる。 特にエチレン一ビニルアルコール共重合体を溶融させて、 溶融紡糸と同 時に不織布を形成させた繊維製品は、 適度な親水性を有し、 安価であることか ら本発明に好適である。繊維状物の繊維径ゃ繊維長については特に制限はなく、 これらは成形物の使用目的に応じて任意に選択することができる。  When used as a fiber product, for example, a fiber obtained by a usual spinning method is further converted into a woven fabric, a knitted fabric or a nonwoven fabric, or a nonwoven fabric is formed directly from a resin by a method such as a spunbond method or flash spinning. Those can be preferably used. In particular, a fiber product obtained by melting an ethylene-vinyl alcohol copolymer to form a nonwoven fabric at the same time as melt spinning is suitable for the present invention because it has moderate hydrophilicity and is inexpensive. There is no particular limitation on the fiber diameter ゃ fiber length of the fibrous material, and these can be arbitrarily selected according to the intended use of the molded product.
繊維製品の具体例としては、 感染性疾患等に罹患した可能性のある患者の体 液に汚染される可能性のある夕オル、 カーテン、 寝間着、 ヘッドカバー、 マス ク、 包帯、 テープ、 アンダーパット、 おしめ、 シーツ、 ガーゼ、 脱脂綿、 ナブ キン、 ティッシュペーパー、 ワイパー (雑巾) 等が例示され、 手術の際に汚染 されるものとして、 手術着、 ドレープ、 シーツ、 患者衣、 エプロン、 ガーゼ、 脱脂綿、 その他が例示され、 更に手術台や手術台周辺の血液を拭き取る拭布等 が例示され、 シングルユーズで廃棄される繊維製品が全て本発明でいう繊維製 品に含まれる。 また、 このような繊維製品は着心地その他の性能改善のために 親水性樹脂以外の樹脂からなる繊維を混綿、 交編織等により混合あるいは積層 してあるものでもよい。  Specific examples of textile products include evening ol, curtains, sleepwear, headcovers, masks, bandages, tapes, underpats, and other materials that may be contaminated with body fluids of patients who may have contracted an infectious disease. Examples include diapers, sheets, gauze, absorbent cotton, napkins, tissue paper, wipers, etc., which may be contaminated during surgery, such as surgical gowns, drapes, sheets, patient clothing, aprons, gauze, absorbent cotton, etc. Further, an operating table and a wiping cloth for wiping blood around the operating table are exemplified, and all textile products discarded in single use are included in the textile products according to the present invention. In addition, such a fiber product may be a product obtained by mixing or laminating fibers made of a resin other than the hydrophilic resin by cotton mixing, cross-knitting or the like in order to improve comfort and other performances.
なお、 本発明の減容化の対象となる廃棄物は、 医療用の各種繊維製品、 医療 検査や食品検査等の機関にて発生する感染性体液等の付着したゴミ、 動物病院 や動物を飼育する施設で発生する人畜共通伝染病を始めとする伝染性病原菌等 を含む廃棄物、 介護施設等で発生する不衛生な廃棄物や衛生害虫 (ダニ等) を 含む廃棄物、 在宅医療の家庭で発生する医療ゴミ、 家庭用品で一見安全そうに 見えても病原性のレジオネラ菌やサルモネラ菌等を含むようなゴミ等のうち、 破壊しなくても減容できるもの、 袋を突き破るような危険物を含まないもので あるが、 それ以外には、 おむつのように異臭を発生するような不快ゴミも含ま れる。 The waste to be reduced in volume according to the present invention includes various textile products for medical use, Garbage with infectious bodily fluids generated by inspection and food inspection institutions, waste containing infectious pathogens such as zoonotic diseases such as zoonotic diseases that occur in animal hospitals and animal breeding facilities, and nursing care facilities Of unsanitary waste and sanitary pests (mite, etc.), medical garbage generated in home care homes, and pathogenic Legionella and Salmonella bacteria that appear safe in household goods. Among the garbage that can be contained, those that can be reduced in volume without destroying them, and those that do not contain dangerous substances such as piercing bags, but other unpleasant garbage that emits an unpleasant odor like diapers Is also included.
本発明に供される医療廃棄物は水分の共存下で減容化されるが、 水を含ませ る操作としては、例えば繊維製品の場合には単に室温で水で濡らすだけでよい。 このために用いる水は単なる水道水でも良いが、 患者の血液や尿やその他の汚 物が混ざった汚水であってもよいし、 手術台周辺の床を清掃する際に用いた水 を繊維製品にて拭き取ったものであってもよいし、 病原菌を殺菌するために消 毒剤を配合した水であってもよい。 この水の加え方に関し、 本発明の水溶性繊 維製品に熱湯を加えると、 熱湯と接触した繊維製品塊の表面のみにゲル層が生 成し、 このゲル層が熱湯の繊維塊内部への侵入を妨げるため減容化の効率が悪 くなることがある。 従って、 繊維製品への水の添加は冷たい水を用いて水をで きるだけ満遍なく繊維製品全体に行き渡らせることが好ましい。  Although the volume of the medical waste provided in the present invention is reduced in the presence of water, the operation of adding water may be, for example, simply wetting with water at room temperature in the case of textiles. The water used for this purpose may be simple tap water, it may be sewage mixed with patient's blood, urine or other contaminants, or water used for cleaning the floor around the operating table may be made of textile. May be used, or water containing a disinfectant to sterilize pathogenic bacteria may be used. Regarding the method of adding water, when hot water is added to the water-soluble fiber product of the present invention, a gel layer is formed only on the surface of the fiber product mass in contact with the hot water, and this gel layer is applied to the inside of the fiber mass of the hot water. The efficiency of volume reduction may be reduced because it prevents intrusion. Therefore, it is preferred that the water be added to the textile using cold water so that the water is distributed as evenly as possible throughout the textile.
本発明の医療用減容性樹脂成形物は、 その使用目的から、 例えばトレ一状容 器に患者から採取した組織を載置した場合に血液が透過して容器以外の物品が 汚染されたり、 また、 手術着やシーツに血液が付着した場合に血液を透過する ことがあってはならない。 その防止策として、 医療用減容性樹脂成形物の表面 または内部に実質的に水不透過の層を設けることが好ましく、 そのためには、 該樹脂成形物が 2枚以上の不織布および/または織布を積層して成型される繊 維製品の場合には、 その表面または内部に水不透過性の層を設けたり、 積層さ れる不織布層を撥水剤で処理するなどして、 耐水性を向上させることが好まし い。 The medical volume-reducing resin molded product of the present invention may be used, for example, when a tissue collected from a patient is placed on a tray-like container, blood permeates to contaminate articles other than the container, Also, if blood adheres to surgical gowns or sheets, it must not penetrate the blood. As a preventive measure, it is preferable to provide a substantially water-impermeable layer on the surface or inside of the medical volume-reducible resin molded product. For this purpose, the resin molded product is made of two or more nonwoven fabrics and / or textiles. In the case of textile products formed by laminating fabrics, water resistance is provided by providing a water-impermeable layer on the surface or inside, or by treating the laminated nonwoven layer with a water repellent. Better to improve No.
本発明の医療用減容性樹脂成形物に設けられる水不透過性の層としては、 水 蒸気は透過しても構わないが、 水滴は透過させない性質を有する必要がある。 このような水不透過性の層を構成する素材はポリオレフィンの不織布であって もよいが、 体温の水によってはその形態が変形することがなく、 熱水又は高温 の水蒸気により収縮または溶解する樹脂であっても良く、 そのような樹脂とし ては軟化点が 5 0〜 1 0 0 °Cの範囲にあるトランスポリイソプレン、 エチレン —酢酸ビニル共重合体、 ポリ力プロラクトン樹脂や可塑剤を含んだポリ酢酸ビ ニル樹脂等が挙げられ、 水溶性樹脂としてはポリビニルアルコール系樹脂から 作製されたフィルムが好ましく用いられる。 また撥水剤としては、 フッ素系撥 水撥油剤、 エチレン尿素系、 メラミン系、 メチロールアミ ド系、 シリコン系等 が挙げられ、 これらの中から任意のものが選択される。  The water-impermeable layer provided in the medical volume-reducible resin molded article of the present invention may have a property of allowing water vapor to permeate but not allowing water droplets to permeate. The material constituting such a water-impermeable layer may be a non-woven fabric of polyolefin, but the resin is not deformed by water at body temperature and is shrunk or dissolved by hot water or high-temperature steam. Such resins include trans polyisoprene having a softening point in the range of 50 to 100 ° C., ethylene-vinyl acetate copolymer, polyproprolactone resin and plasticizer. And a film made of a polyvinyl alcohol resin is preferably used as the water-soluble resin. Examples of the water repellent include a fluorine-based water- and oil-repellent, an ethylene urea-based, a melamine-based, a methylolamide-based, and a silicon-based, and an arbitrary one is selected from these.
繊維製品に含ませる水の量は繊維製品を満遍なく濡らしてはいるが繊維製品 から滴り落ちることはない程度の量が理想的で、 具体的には、 感染性医療廃棄 物 Z水の質量比が好ましくは 7 0 Z 3 0〜2 0ノ8 0であり、 より好ましくは 6 7 / 3 3〜2 5 Z 7 5の範囲である。 水の使用量が多過ぎれば廃棄物の重量 が重くなりすぎ、 さらに減容後に取り出した廃棄物の形状が固形とならず、 取 扱いが厄介となると共に、 後に焼却する際に多量のエネルギーが必要となる。 逆に水の使用量が少な過ぎれば水で濡れていない部位が目立ち、 廃棄物の減容 化率が不十分となる。 しかし、 術者や看護人の汗がアンダーウェア一やガウン 等の繊維製品に吸収され、 この吸収量が無視できないほどに多い場合や、 患者 の発汗、 失禁、 出血によりシート等が濡れた場合には、 新たに添加する水の量 は、 含まれている水分を考慮して、 全体量が上記範囲となるようにするのが好 ましい。  Ideally, the amount of water contained in the textile should be such that it wets the textile evenly but does not drip from the textile.Specifically, the mass ratio of infectious medical waste Z water is It is preferably in the range of 70 Z30 to 20 Z80, and more preferably in the range of 67/33 to 25 Z75. If the amount of water used is too large, the weight of the waste will be too heavy, and the shape of the waste taken out after volume reduction will not be solid, making it difficult to handle, and will require a large amount of energy when incinerated later. Required. Conversely, if the amount of water used is too small, parts that are not wet with water will be conspicuous, and the volume reduction rate of waste will be insufficient. However, when the sweat of the surgeon or nurse is absorbed by textiles such as underwear and gowns, and this amount is not negligible, or when the patient gets wet due to sweating, incontinence, or bleeding of the patient. It is preferable that the total amount of newly added water be within the above range in consideration of the contained water.
この親水性樹脂を湿熱溶融状態にさせる温度は高いほど短時間で溶融状態が 実現するために有利であり、 具体的には 7 0 °C以上が採用され、 好ましくは 9 0 °C以上、 より好ましくは 1 0 0 °C以上であるが 1 5 0 °Cを超えるほどに温度 が高いと高温を発生させるのに要するランニングコス卜が増加することと、 水 の気化に伴う体積膨張が急激かつ著しくて、 装置の運転の制御が困難となる場 合があるため好ましくない。 好ましくは 1 4 0 °C以下である。 The higher the temperature at which the hydrophilic resin is brought into the wet heat melting state, the more advantageous it is to achieve the melting state in a short time. Specifically, 70 ° C. or higher is employed, and preferably 9 ° C. or more. 0 ° C or more, more preferably 100 ° C or more, but if the temperature is higher than 150 ° C, the running cost required to generate a high temperature increases, and water vaporization increases. The resulting volume expansion is rapid and remarkable, which may make it difficult to control the operation of the apparatus, which is not preferable. Preferably it is 140 ° C. or lower.
また、 9 0 °Cを越える温度条件を用いた場合、 感染性廃棄物に含まれる一般 細菌やウィルスが非常に効率よく消毒されて短時間の内に最低発症菌数を下回 り、 湿熱溶融による減容化と同時に感染性の大幅な低減による廃棄物処理の安 全性の向上が利点として挙げられる。  In addition, when temperature conditions exceeding 90 ° C are used, general bacteria and viruses contained in infectious waste are disinfected very efficiently, and the number of affected bacteria falls below the minimum number of bacteria within a short period of time. The advantage is that the safety of waste disposal is improved by the drastic reduction of infectivity as well as the volume reduction by wastewater treatment.
さらに、 また 1 0 o °cを超える温度を用いれば、 水と加熱することにより湿 熱溶融状態にされた医療廃棄物は、 内部の水が気化する圧力によって膨張し、 餅を焼く時に餅が膨れてはじけるような現象を起こすが、 この現象とともに内 部に含まれていた空気が抜けて、 最終的には体積が大きく減少する。  Furthermore, if a temperature exceeding 10 ° C is used, the medical waste that has been made into a wet-heated molten state by heating with water expands due to the pressure of the internal water to evaporate, and the rice cake is formed when the rice cake is baked. A phenomenon such as swelling and popping occurs, but with this phenomenon, the air contained inside escapes and eventually the volume is greatly reduced.
本発明の感染性医療廃棄物は収納袋に収納し、 上記方法にて減容化すること ができる。 本発明で用いる収納袋本体は、 熱可塑性フィルムからなる必要があ り、 本発明の加熱手段の到達する温度に耐える耐熱性熱可塑性フィルムからな るのが好ましい。 このような袋を作製し得る熱可塑性ポリマ一としては、 好ま しくは 1 0 0 °C以上、 より好ましくは 1 0 5 °C以上の耐熱温度をもつ熱可塑性 ポリマーである。 このような素材としては例えばポリオレフインがあり、 中で も高密度ポリエチレン、 中密度ポリエチレン、 ポリプロピレン等が好ましく、 またポリオレフイン以外の低価格の袋用素材としてポリエチレンテレフ夕レー ト (P E T )、 ポリブチレンテレフタレ一ト、 ポリ 卜リメチレンテレフ夕レート 等のポリエステルを挙げることができる。 低密度ポリエチレンは耐熱性が 9 0 °C以下と低く、 本発明の感染性医療廃棄物の減容化用収納袋としては適さな レ^ なお本発明でいう耐熱温度とは A S T M D 7 5 9試験法に準拠して測定 したものを示す。 これらの素材からインフレーション成形法あるいは二軸延伸 法によつて作製されたフィルムから本発明の感染性医療廃棄物の減容化用袋を 生産することができる。 また、 これらの素材が硬すぎて袋の口を縛る時に密閉 性に難がある場合にはそれを軽減するためにナイ口ンその他のラミネートを施 したものを用いてもよい。 The infectious medical waste of the present invention is stored in a storage bag and can be reduced in volume by the above method. The storage bag body used in the present invention needs to be made of a thermoplastic film, and is preferably made of a heat-resistant thermoplastic film that can withstand the temperature reached by the heating means of the present invention. The thermoplastic polymer from which such a bag can be produced is preferably a thermoplastic polymer having a heat resistance temperature of 100 ° C. or more, more preferably 105 ° C. or more. Examples of such a material include polyolefin, and among them, high-density polyethylene, medium-density polyethylene, and polypropylene are preferable, and low-cost bag materials other than polyolefin include polyethylene terephthalate (PET) and polybutylene terephthalate. Examples thereof include polyesters such as sauce and polymethylene terephthalate. Low-density polyethylene has low heat resistance of 90 ° C or less, and is suitable as a storage bag for reducing the volume of infectious medical waste of the present invention. Note that the heat-resistant temperature referred to in the present invention is ASTMD 759 test The values measured according to the law are shown. A bag for reducing the volume of infectious medical waste of the present invention is formed from a film produced from these materials by an inflation molding method or a biaxial stretching method. Can be produced. If these materials are too hard to seal tightly when tying the mouth of the bag, it may be possible to use a plywood or other laminated material to reduce this.
本発明においては、 収納袋本体の側面または開口部に、 病原菌濾過手段が備 えられているが、 濾過手段とは、 感染性の体液が飛び散った飛沫を通さないよ うなフィルター材であり、 例えば病原体を含む血液が微小な液滴となって飛び 散ったものを除去できるものであり、 物理的な濾過以外に吸着作用で濾過を行 うものでもよい。 血液中には直径 1 0 m前後の白血球や赤血球が多数含まれ ており、血液の飛沫はこの血球成分を核として凝集するものと考えられるので、 直径 1 0 m以下の粉塵を除去できる濾過手段を使用することが必要である。 また、 体液の飛沫を水滴の大きさに近似して考えると、 水滴の中でも最も微細 な霧の粒子は直径 1 x m以上であるので、 直径 1 / の粒子を 9 9 %以上除去 できる濾過手段がより好ましい。 当然、 さらに高性能の H E P Αフィルターや U L P Aフィルター、 エレクトレツトフィルターを使用しても何等差し支えな い。 また濾過手段の形状は特に限定されないが、 袋への装着のしゃすさからは、 円筒状あるいはシート状であることが好ましい。  In the present invention, a pathogen filtering means is provided on the side surface or the opening of the storage bag main body, and the filtering means is a filter material which does not allow infectious bodily fluids to pass through. It can remove blood that contains pathogens in the form of fine droplets and scattered, and may be one that performs filtration by adsorption instead of physical filtration. Blood contains a large number of white blood cells and red blood cells with a diameter of about 10 m, and blood droplets are thought to aggregate with these blood cell components as nuclei.Therefore, filtration means that can remove dust with a diameter of 10 m or less can be removed. It is necessary to use Considering the droplets of bodily fluids as approximating the size of water droplets, the finest mist particles among water droplets have a diameter of 1 xm or more.Therefore, filtration means that can remove more than 99% of particles with a diameter of 1 / are used. More preferred. Of course, there is no harm in using a higher performance HEP II filter, ULPA filter, or electret filter. The shape of the filtering means is not particularly limited, but is preferably cylindrical or sheet-like from the viewpoint of ease of attachment to the bag.
これら濾過手段を構成する素材は、 これが焼却された時にあまり灰分を残さ ない方が好ましい。 濾過手段の素材の一例として不織布が挙げられるが、 不織 布は湿式法、 カード法、 スパンボンド法、 メルトブローン法、 フラッシュ紡糸- 法等各種の製法で製造することが可能であるが、 中でも極細繊維からなるメル トブローン法やフラッシュ紡糸法によって製造される不織布は、 均一な微細孔 が多数開いており、 通気性とバクテリア遮断性の点で好ましく、 さらにエレク トレッ卜加工を行ったものは特に好ましい。 フィル夕一部材はポリプロピレン やポリエステル等それ自身撥水性のあるポリマーからなるものか、 あるいは撥 水加工したものが、 表面に水滴が凝着してもフィル夕一の目詰まりが生じない ので好ましい。 フィル夕一部材として使用する不織布は、 一層でも、 また補強 その他の目的で他の不織布や紙、 補強用シー卜等と二層以上積層したものであ つてもよい。 It is preferable that the material constituting these filtering means does not leave much ash when incinerated. An example of a material for the filtration means is a nonwoven fabric.A nonwoven fabric can be manufactured by various manufacturing methods such as a wet method, a card method, a spunbond method, a melt blown method, and a flash spinning method. Nonwoven fabrics made of fiber by melt blown or flash spinning methods have a number of uniform micropores and are preferred in terms of air permeability and bacterial barrier properties.Electret-treated fabrics are particularly preferred. . The filter member is preferably made of a water-repellent polymer such as polypropylene or polyester, or a water-repellent material, since even if water droplets adhere to the surface, the filter member is not clogged. The non-woven fabric used as a material for the film is one layer and reinforced For other purposes, two or more layers may be laminated with another nonwoven fabric, paper, reinforcing sheet, or the like.
本発明においては、 濾過手段に消臭材料を併用してもよく、 例えば、 糞便臭、 腐敗臭、 薬品臭を吸着、 吸収あるいはこれと反応するものが好ましく使用され る。 そのようなものとして活性炭を用いたり、 イオン交換樹脂で作製した不織 布やスポンジ、不揮発性あるいは高沸点の塩基性物質や酸性物質や植物抽出物、 チオールと反応し得る物質等からなる消臭剤の一種あるいはそれ以上を染み込 ませた不織布やスポンジ等を用いることができる。 消臭剤としてはクェン酸や リンゴ酸、 ビタミン Cその他の酸性物質、 炭酸ナトリウム、 ポリエチレンイミ ン、 へキサメチレンテトラミン、 その他の塩基性物質、 ミヨウバン水や含水グ リオキザールその他のチオールと反応し得る物質、 銅クロ口フィンリンナトリ ゥム、 シャンピニオンエキス、 カテキン、 ポリフエノール、 柿抽出エキス、 そ の他の植物抽出物、 シクロデキストリン、 両性界面活性剤、 ァビエチン酸塩類 等が例示される。 また前述のフィルタ一に消臭性能を兼ね備えていれば、 さら に好ましい。  In the present invention, a deodorizing material may be used in combination with the filtering means. For example, those which adsorb, absorb or react with fecal odor, putrefaction odor, and chemical odor are preferably used. Such materials include activated carbon, non-woven fabrics and sponges made of ion-exchange resin, non-volatile or high-boiling basic substances, acidic substances, plant extracts, and substances that can react with thiols. A nonwoven fabric or sponge impregnated with one or more agents can be used. Deodorants include cunic acid, malic acid, vitamin C and other acidic substances, sodium carbonate, polyethyleneimine, hexamethylenetetramine, other basic substances, alum water, hydrous glyoxal, and other substances that can react with thiols , Copper pin mouth finnulin sodium, champignon extract, catechin, polyphenol, persimmon extract, other plant extracts, cyclodextrin, amphoteric surfactant, abietic acid salts and the like. It is even more preferable that the above-mentioned filter also has deodorizing performance.
本発明においては、 減容化処理において、 収納袋内を減圧状態にすることが できるが、 減圧状態の収納袋に外気が侵入しないように濾過手段に逆止弁を装 着することが好ましく、 例えば、 平らなプラスチックあるいはゴム片が平らな 板の上の穴を塞ぐ形式、 ボール弁のように曲面が曲面上に設けられた穴を塞ぐ 形式、 自転車チューブの逆止弁のように管の側面に開けられた穴を弾力性の力 バーが塞ぐ形式等いずれのものでも使用することができる。 また、 濾過手段に 接触する樹脂部材であって内部の空気が抜けた後に該樹脂部材が溶解してフィ ルターを目詰まりさせる形式の不可逆性の弁のようなものであってもよい。 こ の逆止弁もプラスチックやゴム等の有機物により作製され、 焼却した後に灰を 残さないものが好ましく、 できるだけ低価格で供給できるように単純なものが 好ましい。 本発明では、 廃棄物を入れる袋の側面に面状のフィル夕一や消臭手段や逆止 弁を取付けて使用することもできるし、 消臭手段と逆止弁を備えた筒体状の濾 過手段を収納袋の口に装着して使用することもできる。 フィルタ一部材を袋の 側面や筒状濾過手段に取付ける方法としては、 例えばヒートシール法等の熱接 着が好ましいが、 市販の接着剤、 両面テープ、 熱溶融フィルム等の接着材料を 使用してもよい。 熱溶融フィルムとしてはポリ酢酸ビニル、 ポリアミド、 ェチ レンー酢酸ビニル共重合体等が挙げられる。 In the present invention, in the volume reduction process, the inside of the storage bag can be reduced in pressure, but it is preferable to attach a check valve to the filtering means so that outside air does not enter the storage bag in the reduced pressure, For example, a flat plastic or rubber piece closes a hole on a flat plate, a curved surface closes a hole provided on a curved surface like a ball valve, or a side of a pipe like a check valve on a bicycle tube. Any type can be used, such as a type in which a resilient force bar closes a hole formed in a hole. Alternatively, the filter may be an irreversible valve of a type in which the resin member is in contact with the filtering means and the filter is clogged by dissolving the resin member after the internal air is released. This check valve is also preferably made of an organic substance such as plastic or rubber and does not leave ash after incineration, and is preferably simple so as to be supplied at the lowest possible cost. According to the present invention, it is possible to use a sheet filled with waste, a planar filter, a deodorizing means and a check valve attached to the side surface, or a cylindrical body having a deodorizing means and a check valve. The filtering means can be used by attaching it to the mouth of the storage bag. As a method for attaching the filter member to the side of the bag or the cylindrical filtering means, for example, heat bonding such as a heat sealing method is preferable, but using a commercially available adhesive, a double-sided tape, a hot-melt film, or other adhesive material. Is also good. Examples of the hot melt film include polyvinyl acetate, polyamide, and ethylene-vinyl acetate copolymer.
本発明において収納袋の口を密閉する手段としては、 例えば不織布などの積 層体からなるフィル夕一は袋に予め熱接着などにより取付けられている場合、 袋の口をそのまま縛ったり、 袋の口を紐、 ゴム紐、 輪ゴムや粘着ビニールテー プで締め付けるように巻いて密閉する方法が好ましい。 また、 フィルターや消 臭手段や逆止弁を筒体に取付けて一つのユニット (濾過手段) としたものを通 常の袋の口に接続する場合には、 袋の口をすぼめた中心部に筒状のフィルター ュニットを袋の内外を連通する形で保持し、 袋の口をその筒状のフィルターュ ニットを締め付けるような形で囲み、 紐、 ゴム紐、 輪ゴムや粘着ビニールテ一 プを用いて巻いて締め上げる方法が好ましい。  In the present invention, as a means for sealing the mouth of the storage bag, for example, when a filler made of a laminate such as a nonwoven fabric is previously attached to the bag by thermal bonding or the like, the mouth of the bag is tied directly, A preferred method is to wind the mouth tightly with a string, rubber string, rubber band, or adhesive vinyl tape and seal it. If a filter, deodorizing means, or check valve is attached to the cylinder to form a single unit (filtering means) and the bag is connected to the mouth of a regular bag, the mouth of the bag should be in the center of the pursed bag. Hold the cylindrical filter unit so that it communicates with the inside and outside of the bag, enclose the mouth of the bag in such a way as to tighten the cylindrical filter unit, and wind it with a string, rubber string, rubber band, or adhesive vinyl tape. The method of tightening is preferable.
本発明の感染性廃棄物を減容化するために用いる収納袋の構造について、 以 下図面に基づいて説明する。  The structure of the storage bag used to reduce the volume of infectious waste according to the present invention will be described below with reference to the drawings.
第 1図は袋内の気体をフィルタ一を通して外部へ放出することのできる廃棄 物用の袋の一例であり、 Aはこの発明の濾過手段 (3 ) と逆止弁 (4 ) を取付 けた袋の正面図、 Bはフィルター (3 ) と逆止弁 (4 ) の部分の詳細図、 Cは 袋に廃棄物を入れて密閉した後の外観図である。 また第 2図も感染性医療廃棄 物を減容化するために用いる収納袋の一例であり、 Dは収納袋の正面図、 Eは フィル夕一 (3 ) と逆止弁 (4 ) からなり、 臭気吸収材 (7 ) を充填した筒状 のフィルターユニット (濾過手段) の断面図、 Fは Dの収納袋に廃棄物を入れ た後に収納袋の開口部に Eのフィルターユニッ ト (濾過手段) を装着して袋を 密閉した図である。 Fig. 1 shows an example of a bag for waste that can release the gas in the bag through a filter. A is a bag equipped with the filter means (3) and the check valve (4) of the present invention. B is a detailed view of the filter (3) and the check valve (4), and C is an external view of the bag after putting waste into a bag and sealing it. Fig. 2 also shows an example of a storage bag used to reduce the volume of infectious medical waste. D is a front view of the storage bag, and E is a filter consisting of a filter (3) and a check valve (4). A cross-sectional view of a cylindrical filter unit (filtration means) filled with odor absorbing material (7). F shows the filter unit of E (filtration means) in the opening of the storage bag after waste is put in the storage bag of D. ) Put on the bag FIG.
この感染性医療廃棄物の運搬を容易にする方法の一つの応用として、 前述の 親水性樹脂のみを使用して減容化するのはなく、 例えば親水性樹脂からなるシ ーッゃガウンの中に親水性ではない感染性廃棄物を包み込んで減容化すること も推奨される。 すなわち、 親水性樹脂成形物に通常のプラスチック容器や注射 筒や手袋等の手術室で発生する種々の感染性廃棄物を混合した状態で、 親水性 樹脂成形物の減容化を行っても良い。 この場合、 感染性医療廃棄物の全質量に 対し、 親水性樹脂成形物を 2 0 %以上、 好ましくは 3 3〜 9 9 %と、 親水性樹 脂に対して親水性樹脂製品に含まれる水の量として 4 3〜4 0 0質量%、 好ま しくは 5 0〜3 0 0質量%となるように水を混合し、 7 0〜 1 5 0 °Cの温度に て該親水性樹脂成形物を溶融させ、 親水性樹脂成形物の体積を減少させると同 時に、 親水性樹脂以外の感染性医療廃棄物の隙間や内部に湿熱溶融状態の親水 性樹脂を流れ込ませてバインダ一とし、 感染性医療廃棄物全体を一つのプロッ クとして固定することができる。 この方法には、 親水性樹脂成形物自身の減容 化に起因する体積減少と、 例えば注射筒やサンプル管の内部にも水蒸気が充満 し、 それが冷える時に真空状態を作つてそこに湿熱溶解した樹脂が入り込むこ とによる体積減少とが同時に起こることによる減量化のメリッ卜と、 万が一、 医療事故を引き起こす可能性のある注射針やメスの替刃等が混入していたとし ても、 それらはブロックの内部に固定されて動けなくなることから、 人を傷つ ける可能性が大きく減少するといぅメリッ卜がある。  One application of this method of facilitating the transport of infectious medical waste is to reduce the volume by using only the aforementioned hydrophilic resin. It is also recommended to wrap up infectious waste that is not hydrophilic to reduce its volume. That is, the volume of the hydrophilic resin molded article may be reduced in a state where various infectious wastes generated in the operating room, such as ordinary plastic containers, syringes, and gloves, are mixed with the hydrophilic resin molded article. . In this case, the hydrophilic resin molded product accounts for at least 20%, preferably 33 to 99% of the total mass of infectious medical waste, and the water contained in the hydrophilic resin product relative to the hydrophilic resin. Of the hydrophilic resin at a temperature of 70 to 150 ° C. by mixing water so that the amount becomes 43 to 400% by mass, preferably 50 to 300% by mass. At the same time as reducing the volume of the hydrophilic resin molded product, and at the same time, injecting the wet-heat-melted hydrophilic resin into the gaps and inside of the infectious medical waste other than the hydrophilic resin to form a binder, The entire medical waste can be fixed as one block. This method involves reducing the volume due to the volume reduction of the hydrophilic resin molded product itself and, for example, filling the inside of the syringe or sample tube with water vapor, creating a vacuum when it cools down, and dissolving wet heat there. The advantage of weight reduction due to the simultaneous volume reduction caused by the infiltration of the injected resin, and the fact that even if needles and scalpel blades that could cause medical accidents are mixed in, There is a merit that the possibility of injuries is greatly reduced because the block is fixed inside the block and cannot move.
なお、 本発明でいう感染性医療廃棄物とは、 感染性物質により汚染されてい る医療廃棄物のほかに、 感染性物質により汚染されている可能性のある医療廃 棄物を包含している。  The infectious medical waste referred to in the present invention includes not only medical waste contaminated with infectious substances but also medical waste possibly contaminated with infectious substances. .
減容化処理工程により感染性医療廃棄物、 特に医療用繊維製廃棄物の見かけ 体積は大きく減少するが、 水が理想的に行き渡れば減容化前の嵩比重に関わら ず、 減容化処理後の廃棄物の比重は 1 . 1〜 1 . 2程度となり、 減容化率はひ とえに繊維製廃棄物が廃棄物容器に捨てられた時の嵩高さに左右されるもので ある力 かなりコンパクトなもので 1 / 2以下、 非常に嵩張るもので 1ノ 2 0 程度である。 The apparent volume of infectious medical waste, especially medical fiber waste, is greatly reduced by the volume reduction process, but if water is ideally distributed, it will be reduced regardless of the bulk density before volume reduction. The specific gravity of the treated waste is about 1.1 to 1.2, and the volume reduction rate is high. Even so, the strength depends on the bulkiness of the fiber waste when it is thrown into a waste container. It is a very compact one-half or less, and the very bulky one is about 20.
次に、 本発明の方法を実施するのに好適な感染性医療廃棄物用減容装置 (以 下、 減容装置と称する) について図面に基づき説明する。  Next, a volume reducing device for infectious medical waste suitable for carrying out the method of the present invention (hereinafter referred to as a volume reducing device) will be described with reference to the drawings.
本発明の減容装置は、 基本的には、 第 3〜 5図に示すように、 筐体 (1 ) と、 加熱室 (2 ) と、 加熱手段 (3 ) と、 加熱手段に送る熱の供給を制御、 具体的 に電力の供給を制御する手段とからなるものである。 しかし、 この装置をさら に使い易くするために、 前述の要素に加えて、 加熱釜 (4 ) と、 湿熱溶融され ている樹脂の状態を検出して前述の電力供給制御手段に信号を送るための検出 手段を設けることもできる。  Basically, as shown in FIGS. 3 to 5, the volume reduction device of the present invention comprises a housing (1), a heating chamber (2), a heating means (3), and a heat source to be sent to the heating means. Means for controlling the supply, and specifically for controlling the supply of power. However, in order to make this device even easier to use, in addition to the above-mentioned elements, it is necessary to detect the state of the heating pot (4) and the resin melted by wet heat and send a signal to the above-mentioned power supply control means. Detection means can be provided.
この減容装置には、 加熱手段としてマイクロ波を用いるのが好ましいが、 マ イク口波を用いる場合には、 この減容装置から発生する電磁波の放散を防ぐた めに、 電磁波を遮蔽あるいは吸収する機能を付与することが好ましい。 電磁波 を遮蔽あるいは吸収することにより、 減容装置の周りに設置されている医療機 械が誤操作することを防止することができる。 この電磁波を遮蔽あるレ ^は吸収 するために使用する技術としては、 筐体を導電性の良い金属板製としたり、 金 属板製でない筐体の場合には筐体主要部に金属のメッシュゃ箔を貼り付けると 力、、 金属を溶着したりメツキしたりしてアースをとるとか、 金属やカーボン等 の導電性繊維や導電性粉末を含む導電性プラスチックを使用するとか、 フェラ イ トのような電磁波を吸収する物質を含む塗料を使用するとかの方法があり、 これらの技術の一つあるいは幾つかを組合せて使用する。 あるいは、 さらに完 璧を期するためにこの減容装置を別の導電性ケースや導電性シートで覆ったり してもよい。  It is preferable to use microwaves as the heating means in this volume reduction device, but if a microphone mouth wave is used, the electromagnetic waves are shielded or absorbed in order to prevent radiation of the electromagnetic waves generated from this volume reduction device. It is preferable to provide the function of By shielding or absorbing the electromagnetic waves, medical devices installed around the volume reduction device can be prevented from being erroneously operated. Techniques used to absorb this electromagnetic wave are as follows: the case is made of a metal plate with good conductivity, or if the case is not made of metal plate, the main part of the case is made of metal mesh.ゃ When the foil is pasted, the grounding is performed by welding or plating metal, the use of conductive plastics containing conductive fibers such as metal or carbon or conductive powder, or the use of ferrite. There is a method such as using a paint containing a substance that absorbs electromagnetic waves, and one or some of these techniques are used in combination. Alternatively, the volume reduction device may be covered with another conductive case or conductive sheet for further perfection.
本発明の減容装置には加熱室 (2 ) を有することが必要であり、 筐体ととも に該加熱室を形成する蓋体 (5 ) が開閉自在に取付けられており、 該蓋体 (5 ) もしくは筐体 (1 ) には作業員の火傷を始めとする種々の危険を回避するため に、蓋体の開放を検知し電源を遮断するためのマイクロスィツチが設けられる。 この加熱室内には加熱釜 (4 ) が着脱自在に載置あるいは固着されてもよい。 この加熱釜 (4 ) には、 減容処理温度に耐えうるポリエチレン製またはポリプ ロピレン製その他の耐熱性の袋 (6 ) をかぶせて加熱釜の汚染を防ぐことがで き、加熱釜(4 )が汚れた場合には加熱釜を加熱室から外部に取り外して清掃 · 消毒することができる。 さらに、 この加熱釜にはこれを回転あるいは振動させ る手段と連結可能として、 湿熱溶融状態の廃棄物に運動エネルギーを与えるこ とにより、 空気の抜けを加速することができるし、 フックやキネで攪拌したり 突いたりして空気を追い出しても良い。 The volume reduction device of the present invention needs to have a heating chamber (2), and a lid (5) that forms the heating chamber is attached to the housing together with the housing so as to be openable and closable. Five ) Alternatively, the housing (1) is provided with a microswitch for detecting the opening of the lid and shutting off the power in order to avoid various dangers such as burns of the workers. A heating pot (4) may be detachably mounted or fixed in the heating chamber. The heating pot (4) can be covered with a polyethylene or polypropylene heat-resistant bag (6) that can withstand the volume reduction temperature to prevent contamination of the heating pot (4). If it becomes dirty, the heating pot can be removed from the heating chamber and cleaned and disinfected. In addition, this heating pot can be connected to a means for rotating or vibrating it, and by applying kinetic energy to the waste heat in the wet heat state, the air can be accelerated to escape, and hooks and kinetics can be used. The air may be expelled by stirring or poking.
また、 廃棄物に加えられた水が加熱室の中で凝縮してできた水や、 加熱のた めに加えられたスチームが加熱室の中で凝縮してできた水が加熱室の中に溜ま る現象に対処したり、 加熱室の中を洗浄 ·消毒する際に汚水を排出するのに便 利なように、 排水口と排水用配管を設けてもよい。 また、 この加熱室を減圧条 件にもなし得るように、 排気配管 (9 ) の途中に真空ラインと接続する手段や コック等が設けられていてもよい。  In addition, water that is added to the waste and condensed in the heating chamber and water that is added for heating and condensed in the heating chamber are added to the heating chamber. Drainage outlets and drainage pipes may be provided to deal with pooling phenomena and to drain sewage when cleaning and disinfecting the heating chamber. Further, a means for connecting to a vacuum line, a cock, or the like may be provided in the exhaust pipe (9) so that the heating chamber can be operated under a reduced pressure condition.
本発明の減容装置には加熱手段が必要であり、 この加熱手段としてはマイク 口ウェーブ、 スチーム、 電熱線、 赤外線等が挙げられる。 これらの中でもマイ クロウエーブが最も短時間で廃棄物の温度を上げることができるため好ましい 力 スチームを用いて滅菌を兼ねながら減容化するものであっても良い。 第 3 〜 5図で用いられている加熱手段はマイクロウエーブであり、 マイクロゥェ一 ブ発生器 (3 ) により発生されたマイクロウエーブ (1 0 ) は加熱室 (2 ) 内 の加熱釜 (4 ) 内に入れられた廃棄物と水 (1 2 ) を加熱することとなる。 な お図 5において、 1 6は減容化処理により発生した異臭を吸着する吸着室であ る。  The volume reducing device of the present invention requires a heating means. Examples of the heating means include a microphone opening wave, steam, a heating wire, and infrared rays. Of these, microwaves can increase the temperature of the waste in the shortest time, and may be one that reduces the volume while using sterilization with a preferable force steam. The heating means used in FIGS. 3 to 5 is a microwave, and the microwave (10) generated by the microwave generator (3) is provided in the heating pot (4) in the heating chamber (2). The waste and water (1 2) put in the tank will be heated. In FIG. 5, reference numeral 16 denotes an adsorption chamber for adsorbing an unusual odor generated by the volume reduction treatment.
本発明の減容装 Kには樹脂の状態を検出するための検出手段が必要であり、 かかる検出手段としては赤外線、 あるいは接触式の温度検出器 (1 3 )、 あるい は光学式、 接触式、 超音波式のレベル検出器 (1 4 ) が挙げられる。 前者の温 度検出器は加熱手段が正常に作動していることを確認し、 加熱手段に適切な電 力を供給させるためのものであるが、 さらに重要な目的は、 湿熱溶融状態の樹 脂の温度が上がりすぎて火災発生につながるのを防ぐことである。 後者のレべ ル検出器は減容化操作中の湿熱溶融状態の樹脂が水の蒸気圧のために過度に膨 張して、 加熱室内壁を汚染するのを防ぐため、 液面レベル検出器で一定レベル の膨張が検出された時に加熱手段への電力の供給を制限あるいは停止するもの である。 The volume reduction device K of the present invention requires a detection means for detecting the state of the resin, Examples of such detection means include an infrared or contact temperature detector (13), or an optical, contact, or ultrasonic level detector (14). The former temperature detector is used to confirm that the heating means is operating normally and to supply appropriate power to the heating means. The purpose of this is to prevent the temperature from rising too high and leading to a fire. The latter level detector is a liquid level detector to prevent the resin in the wet heat molten state during volume reduction operation from expanding excessively due to the vapor pressure of water and contaminating the inside of the heating chamber. When a certain level of expansion is detected, the power supply to the heating means is limited or stopped.
電力の供給を制御する手段は温度調整機能やタイマー機能を有するものであ るが、 前述の各種検出手段からの異常信号を基に加熱手段への電力の供給をシ ャットダウンあるいは制限する機能を有するものである。 さらに、 加熱手段の 故障とか、 加熱室内の過熱を検知してアラームを発したり、 減容化の 1サイク ルが終わった旨の信号を発する機能を有するものであってもよい。 なお第 3図 において、 加熱釜は均一に加熱されるようターンテーブル (1 5 ) 上に載せら れている。  The means for controlling the power supply has a temperature adjustment function and a timer function, but has a function to shut down or limit the power supply to the heating means based on the abnormal signals from the various detection means described above. Things. Further, it may have a function of detecting a failure in the heating means or overheating in the heating chamber and issuing an alarm, or a signal indicating that one cycle of volume reduction has been completed. In FIG. 3, the heating pot is placed on a turntable (15) so as to be uniformly heated.
更に本発明に用いる減容装置としては、 第 6図に示すような、 仕込み用ホッ パー (2 1 ) から廃棄物と水 (1 2 ) を加熱部 (2 2 ) に送り込み、 スクリュ ゥにより加熱部内を移動させる間に廃棄物を加熱可塑溶融させ、 加熱部から取 り出す装置でもよい。 また第 7図に示すような、 加熱室 (2 ) 内に、 廃棄物を 入れたドラム (2 3 ) が回転し、 下方から熱源 (2 4 ) により加熱された水蒸 気がドラム壁を通り廃棄物を可塑化すると共に減容化するような装置であつて もよい。 これら図中 2 5は水、 2 6はコントローラ一である。 なお第 6図の装 置において、 加熱部 (2 2 ) は覆われており、 したがって加熱部は筐体 (1 ) とみなせるものである。  Further, as the volume reducing device used in the present invention, as shown in FIG. 6, waste and water (1 2) are fed into a heating section (2 2) from a charging hopper (2 1) and heated by a screw ゥ. It may be a device that heats and melts waste while moving it inside the section and removes it from the heating section. Also, as shown in Fig. 7, the drum (23) containing waste is rotated in the heating chamber (2), and water vapor heated by the heat source (24) passes from below through the drum wall. It may be a device that plasticizes and reduces the volume of waste. In these figures, 25 is water and 26 is a controller. In the apparatus shown in FIG. 6, the heating section (2 2) is covered, so that the heating section can be regarded as a housing (1).
さらに本発明に用いる減容装置としては、 第 8図に示すような、 廃棄物 (1 2 ) をホッパー (2 1 ) に投入し、 ホッパー下のローラ対 (3 7 ) によりシュ レツダータイプの裁断機(3 1 )に送り込んで裁断し、裁断物を下の加熱室( 2 ) 内の加熱釜 (4 ) に落とすとともに、 スチーム又は水を吹付け (3 2 )、 そして、 加熱釜 (4 ) の下に設置した発熱体 (3 3') により所定の温度に加熱する装置 であってもよい。 この装置では、 裁断機部分も含めて装置全体が筐体 (1 ) と なっており、 また発熱体 (3 3 ) は加熱釜内部の温度が調節できるように電力 の供給を制御できるようになつている。 Further, as the volume reducing device used in the present invention, as shown in FIG. 2) is put into the hopper (2 1), and fed to the shredder type cutting machine (3 1) by the roller pair (3 7) under the hopper to be cut, and the cut material is heated in the lower heating chamber (2). A device that drops into the kettle (4), sprays steam or water (32), and heats to a predetermined temperature by the heating element (33 ') installed under the heating kettle (4). Good. In this device, the entire device including the cutting machine is a casing (1), and the heating element (33) can control the power supply so that the temperature inside the heating pot can be adjusted. ing.
さらに第 9図の装置も本発明装置の一例である。 すなわち、 第 9図の装置は、 廃棄物 (1 2 ) をホッパー (2 1 ) に投入し、 ホッパー内 (2 1 ) にスチーム ( 3 2 ) を吹き込み、 必要により水を加え、 ホッパー下のローラー対 (3 7 ) で廃棄物を溶かして粘ちような液として、 下に落とし、 下の容器に受ける装置 であり、 図中 (3 4 ) は水タンク、 (3 5 ) はスチーム発生器、 (3 6 ) は廃棄 物レベルセンサ一である。 この図 9の装置では、 ホッパーが加熱部、 ホッパー 及びローラー対及び下の受容器が筐体、 加熱手段がスチーム、 スチーム発生器 が電力の供給を制御することにより、 供給スチーム量及びホッパー温度を調整 するシステムとなっている。 また、 廃棄物がホッパー内に存在しているか否か を光学的に検出し、 ローラーの回転とスチームのオン ·オフを制御する構造に なっていてもよい。 これら装置においても、 加熱部は覆われていることから、 筐体の中に加熱部が存在しているとみなすことができる。  The apparatus shown in FIG. 9 is also an example of the apparatus of the present invention. That is, in the apparatus shown in Fig. 9, the waste (1 2) is put into the hopper (2 1), steam (32) is blown into the hopper (2 1), and water is added as necessary. This is a device that dissolves waste as a viscous liquid in pairs (37), drops it down, and receives it in the lower container. In the figure, (34) is a water tank, (35) is a steam generator, (36) is a waste level sensor. In the apparatus shown in Fig. 9, the hopper controls the supply of steam and the hopper temperature by controlling the supply of electric power by controlling the power supply with the hopper as the heating section, the hopper and the roller pair and the lower receiver as the housing, the heating means as the steam, and the steam generator as the power supply. It is a system to adjust. Also, a structure that optically detects whether or not waste is present in the hopper and controls the rotation of the roller and the on / off of steam may be employed. Also in these devices, since the heating section is covered, it can be considered that the heating section exists in the housing.
本発明により、 減容化された廃棄物は、 高い温度の状態では粘稠な液体であ るが、 室温まで冷却された場合には、 殆ど流動性を有していない固形物となつ ており (本発明でいう固形物とは、 常温で流動性を有していない状態の他に、 これを常温で容器に入れた場合に、 容器を倒しても瞬時には容器から流れ出る ことがない状態、 いわゆる高粘性の状態も包含している)、 したがって取り扱い が極めて簡単である。  According to the present invention, the volume-reduced waste is a viscous liquid at a high temperature, but becomes a solid having almost no fluidity when cooled to room temperature. (Solids referred to in the present invention are those that have no fluidity at room temperature, and that, when placed in a container at room temperature, do not instantaneously flow out of the container even if the container is knocked down. And so-called high-viscosity conditions), and is therefore extremely easy to handle.
本発明の医療用減容性樹脂成形物の減容化処理は、 感染性医療廃棄物が発生 する医療の現場で行われるのが一般的であるが、 その現場を若干離れた手術室 や病室の廊下、 病院の出入口、 病院の外の空き地などで行われてもよく、 さら には次善の策として、 収集車に大量の廃棄物を積載して運搬できるようにする ために、 該収集車の中で減容化処理を行った後、 廃棄物を運搬してもよい。 この減容化処理を行った後の医療廃棄物は、 特に高温で焼却し得る専 用の焼却設備を用いて焼却処分あるいは熱分解ガス化される。 The volume reduction treatment of the medical volume-reducible resin molded product of the present invention generates infectious medical waste. It is generally performed at a medical site, but it may be performed in an operating room, a corridor of a hospital room, a hospital entrance, a vacant lot outside the hospital, etc., a little further away from the site, and further suboptimally. As a countermeasure, the waste may be transported after performing volume reduction processing in the collection vehicle so that a large amount of waste can be loaded and transported on the collection vehicle. After performing this volume reduction treatment, the medical waste is incinerated or pyrolyzed into gas using a special incineration facility that can be incinerated particularly at high temperatures.
次に本発明を具体的に実施例で説明するが、 本発明は実施例に限定さ れるものではない。 なお本発明での減容性医療用樹脂成形物の減容化テ ス トは、 以下に示す方法により行った。  Next, the present invention will be specifically described with reference to examples, but the present invention is not limited to the examples. In addition, the volume reduction test of the volume-reducible medical resin molded product in the present invention was performed by the following method.
[減容化テスト] : 不織布形状の樹脂成形物を 1 0 0 m Lサンプル管に 詰め込み、 約 5 0 0 gの荷重をかけながらその時の高さを測定して体積 を算出した (V D ) 。 次に所定量の熱湯を該樹脂成形物の上から注ぎ、 熱湯が十分浸透した後 (約 5分後) 、 さらに試験前にかけたのと同じ荷 重をかけて成形物を押し込んで高さを測定し、 体積を算出した (V w) 。 得られた V Dと V wの比 V w Z V Dを算出し評価を行った。 [Volume reduction test]: A non-woven resin molded product was packed into a 100 mL sample tube, and the height was measured while applying a load of approximately 500 g to calculate the volume (V D ) . Next, a predetermined amount of hot water is poured from above the resin molded product, and after the hot water has sufficiently penetrated (after about 5 minutes), the molded product is further pressed in under the same load as before the test, and the height is increased. It was measured and the volume was calculated (V w ). To calculate the ratio V w ZV D evaluation of the resulting V D and V w was carried out.
実施例 1 Example 1
重合度 3 0 0、 ケン化度 9 8 . 5モル%、 エチレン含量 1 0モル%の エチレン一ビニルアルコール共重合樹脂を原料とし、 スパンボンド法に より作成した目付 3 5 g Z m 2の不織布を用い、不織布のみかけ体積(V D ) に対して 8 0 °Cの熱湯を 1 0 %の体積を注ぎ込んで前述の減容化テ ストを行った。 結果を表 ].に示すが、 熱湯を注ぎ込むことにより、 みか けの体積をおよそ 3分の 1にまで減少させることができた。 Polymerization degree of 3 0 0, saponification degree 9 8.5 mol%, the ethylene content 1 0 mole percent ethylene one vinyl alcohol copolymer resin as a raw material, basis weight 3 of 5 g Z m 2 nonwoven created More spunbond method The above volume reduction test was performed by pouring 10% of hot water at 80 ° C. with respect to the apparent volume (V D ) of the nonwoven fabric. The results are shown in Table]. By pouring boiling water, the volume of mikaki was reduced to about one-third.
実施例 2〜 4 Examples 2 to 4
実施例 1 と同様の不織布を用い、 熱湯の条件を表 1に示す量および温 度にして減容化テス トを実施した。 結果を表 1 に示す。  Using the same nonwoven fabric as in Example 1, the hot water conditions were set to the amounts and temperatures shown in Table 1, and a volume reduction test was performed. Table 1 shows the results.
熱湯の量を増やすことでさらに体積が減少し、 成形物のみかけの体積 に対して 3 0 %の量の熱湯で体積が 4分の 1にまで減少した。 Increasing the amount of boiling water further reduces the volume, and the apparent volume of the molded product In comparison, the volume was reduced by a factor of 4 with 30% hot water.
また、 熱湯の温度を 6 O :に下げた場合、 8 0でに比べて体積減少率 がやや低下した。  Also, when the temperature of the hot water was reduced to 6 O :, the volume reduction rate was slightly lower than at 80.
実施例 5および 6 Examples 5 and 6
実施例 1 と同様のポリビニルアルコール樹脂を原料とし、 不織布の目 付を表 1に示すものに変更した以外は実施例 1 と同様の熱湯条件で減容 化テストを実施した。 結果を表 1に示す。  A volume reduction test was performed under the same hot water conditions as in Example 1 except that the same polyvinyl alcohol resin as in Example 1 was used as a raw material, and the basis weight of the nonwoven fabric was changed to that shown in Table 1. Table 1 shows the results.
比較例 1 Comparative Example 1
実施例 1のポリビニルアルコール樹脂からなる不織布の代わりに、 ポ リプロピレン樹脂からなる目付 3 0 g /m 2のスパンポンド不織布を用 レ 実施例 1 と同様の熱湯条件で減容化テストを実施した。 結果を表 1 に示す。 熱湯が不織布中に全く吸収されず、体積変化はみられなかった。 比較例 2 In place of the nonwoven fabric made of the polyvinyl alcohol resin of Example 1, a spun-pound nonwoven fabric having a basis weight of 30 g / m 2 made of a polypropylene resin was used. レ A volume reduction test was performed under the same hot water conditions as in Example 1. . Table 1 shows the results. Hot water was not absorbed into the nonwoven fabric at all, and no change in volume was observed. Comparative Example 2
比較例 1 と同様の不織布を用い、 熱湯を表 1に示す量および温度にし て減容化テストを実施した。 結果を表 1に示す。 比較例 1 と同様、 体積 変化は全く示さなかった。 A volume reduction test was performed using the same nonwoven fabric as in Comparative Example 1 with the amount and temperature of hot water shown in Table 1. Table 1 shows the results. As in Comparative Example 1, no change in volume was shown.
表 1 table 1
Figure imgf000023_0001
実施例 7
Figure imgf000023_0001
Example 7
実施例 1 と同様の不織布を手.術用ガウンと同じ質量 (2 0 0 g ) の四 角い布地とし、 これを折りたたまないまま丸めて感染性廃棄物用の 4 5 Lの高密度ポリエチレン製袋に入れたところ、 9枚で一杯になった。 こ の袋の中にスチームを満遍なく吹き込んで不織布にスチームを吸収させ. 全体の質量が 1 3 0 0 g増加したところでスチームの吹き込みを止め、 足で何度も踏みつけて圧迫して空気を抜くと、 袋の中の不織布は約 5 L に縮まった。 この結果得られた塊を 5 0 0 Wの電子レンジ [ (株) 東芝 製、 E R— 2 4 0 (W) ] に入れ、 3 0秒間マイクロ波を照射して餅が 膨れるように膨張させ、 電子レンジから取り出して再度踏みつけて空気 を抜くと、 この塊の体積は 4 Lに減少した。 (加熱時内の電子レンジ内 の温度は 9 0〜: 1 1 0 °Cの範囲であった。 ) 実施例 8 The same non-woven fabric as in Example 1 was hand-made into a square cloth of the same mass (200 g) as the surgical gown, which was rolled unfolded and made of 45 L high-density polyethylene for infectious waste. When I put it in my bag, it was filled with nine pieces. Steam is evenly blown into this bag to absorb the steam into the non-woven fabric. When the total mass increases by 1300 g, stop blowing the steam and press the foot many times to squeeze and release the air. However, the non-woven fabric in the bag shrank to about 5 L. The resulting mass is placed in a 500 W microwave oven [ER-240 (W), manufactured by Toshiba Corporation], and irradiated with microwaves for 30 seconds to expand the rice cake so that the rice cake expands. The volume was reduced to 4 liters when removed from the microwave and stomp again to deflate. (The temperature in the microwave during heating was in the range of 90 to 110 ° C.) Example 8
重合度 1 5 0 0、 ゲン化度 9 8. 5モル%、 エチレン含量 5モル%の 溶解温度 7 5 :、 水分率 1 1 %のエチレン一ビニルアルコール共重合樹 脂に可塑剤としてポリエチレングリコール 3 0 0を 5質量%添加した混 合物を原料とし、 縦 1 0 c m、 横 2 0 c m、 深さ 2 c m、 厚み 1. 5m mのトレ一を作った。 この箱の占める見かけの体積は 4 0 0 c m3であ つた。 このトレーを外科手術の際に手術で使用したメスやハサミ等を入 れる容器として使用した。 使用後のトレーに 5分間水を入れておき、 2 0秒間実施例 7と同一の電子レンジにかけて軟化させ、 2枚の厚板の間 に挟んで 6 0 k gの荷重をかけたところ、 その体積は 7 0 c m3に縮ま つた (加熱時の電子レンジ内の温度は 9 0〜1 1 0°Cの範囲であった) 。 実施例 9 Polymerization degree 1500, degree of genification 98.5 mol%, ethylene content 5 mol% Melting temperature 75: water content 11% ethylene-vinyl alcohol copolymer resin polyethylene glycol 3 as plasticizer Using a mixture containing 5% by mass of 0 as a raw material, a tray having a length of 10 cm, a width of 20 cm, a depth of 2 cm, and a thickness of 1.5 mm was prepared. The apparent volume occupied by this box was 400 cm 3 . This tray was used as a container for scalpels, scissors, etc. used in the surgery during surgery. The tray after use was filled with water for 5 minutes, softened in the same microwave oven as in Example 7 for 20 seconds, and sandwiched between two thick plates and subjected to a load of 60 kg. 0 cm 3 to shrink ivy (temperature in the microwave oven during heating was in the range of 9 0~1 1 0 ° C). Example 9
( 1 ) エチレン 5モル%共重合した溶解温度 8 0 、 水分率 9. 1 %の エチレン一ビニルアルコール共重合体製の目付 3 5 gZm2の不織布に 8 0 °C溶解のポリビニルアルコール [ (株) クラレ製 PVA— 1 1 7、 水分率 1 0. 6 %] 製フィルムをラミネートした目付 6 O gZm2のシ —トを幅 1 0 0 c m、 長さ 2 0 0 c mに切断してシーツを作製した。(1) Ethylene 5 mole% copolymerized with dissolution temperature 8 0, water content 9.1% ethylene one vinyl alcohol copolymer made of basis weight 35 of GZm 2 nonwoven 8 0 ° polyvinyl alcohol C dissolved [(strain ) manufactured by Kuraray Co. PVA-1 1 7, sheet of water content 10.6% made film basis weight 6 was laminated O gZm 2 - DOO width 1 0 0 cm, the sheets were cut to a length 2 0 0 cm Produced.
(2 ) 第 2図に示すような、 夕テ 40 5 mmxョコ 6 6 0 mm、 厚みが 3 0 mの最大容量が 2 0リッ トルの高密度ポリエチレンからなる感染 性廃棄物用の袋を作製した。 (2) As shown in Fig. 2, a bag for infectious waste consisting of high-density polyethylene with a maximum capacity of 20 liters with a maximum capacity of 20 liters and a width of 405 mm x width 660 mm and thickness of 30 m as shown in Fig. Produced.
( 3 ) 次に、 高密度ポリエチレンからなる内径 1 3 mm、 長さ 6 c mの 円柱状の筒の一端に第 1図 Bのような、 ポリプロピレンをメルトブロー して得られた平均繊維径 3 mで目付が 1 0 g/m 2の不織布と木材パ ルプを抄紙法により加工して目付を 1 0 gノ m2とした積層シー卜から なる、 面積が 5 c m2の袋内の気体を外部に放出するためのフィルター を取付け、 筒内にリンゴ酸を含浸させた脱脂綿と、 含水ダリオキザ一ル を含浸させた脱脂綿とを詰め込み、 そして他端にポリプロピレン製の台 座とゴム片よりなる逆止弁をホッ トメルト接着により取付け、 第 2図に 示すようなフィルターュニッ トを作製した。 (3) Next, as shown in Fig. 1B, one end of a cylindrical tube made of high-density polyethylene with an inner diameter of 13 mm and a length of 6 cm was melt blown with polypropylene, and the average fiber diameter was 3 m. basis weight is processed mass per unit area of a laminated Sea Bok was a 1 0 g Roh m 2 and the paper making method 1 0 g / m 2 nonwoven and wood pulp, the gas in the bag area of 5 cm 2 to the outside Equipped with a filter for release, absorbent cotton impregnated with malic acid in the cylinder, and hydrated darioxal A cotton wool impregnated with the rubber was packed in, and a check valve consisting of a polypropylene pedestal and a rubber piece was attached to the other end by hot melt bonding to produce a filter unit as shown in FIG.
(4) 上記 ( 1 ) で得られたシーツを肝炎患者のベッ トのシーツとして 4日間使用した後、 第 3図の加熱釜に上記 ( 2 ) で得られたポリエチレ ンの袋を被せた中に水 8 OmLを入れ、 この上に上記シーツを緩く丸め て入れた。 この時、 緩く丸めたシーツは 1. 5 Lの体積を占めた。 さら に水 9 OmLを満遍なく注ぎ、 袋の開放端部分を上記 ( 3 ) で作製した フィルターュニッ 卜に巻きつけ、 第 2図に示すようにゴム紐で締め付け て袋の口を密閉した。 加熱釜を加熱室に戻し、 5 0 0 Wのマイクロ波を 照射した。 マイクロ波照射中、 袋は大きく膨張したが、 フィル夕一ュニ ッ トの出口より水蒸気が勢いよく吹き出し、 袋は破裂しなかった。 マイ クロ波照射後直ちに取り出し、 すぐに熱電対 (C u s t orn社、 デジ夕 ルサーモメーター CT— 7 0 0 S) で温度を測定したところ、 9 0 を 示した。 このこと及び照射時の内容物の状態から釜の内部温度は 9 0〜 1 1 0 °Cの範囲に達していた。 取り出し後のシーツは体積が 3 3 OmL まで減少しており、 マイクロ波処理前に比較して 1 Z 5に減容した。 (4) After using the sheets obtained in (1) above as bed sheets of a hepatitis patient for 4 days, place the polyethylene bag obtained in (2) above on the heating pot shown in Fig. 3. Then, 8 OmL of water was added thereto, and the above-mentioned sheets were loosely rounded and put thereon. At this time, the loosely rolled sheets occupied a volume of 1.5 L. Further, 9 OmL of water was poured evenly, the open end of the bag was wrapped around the filter unit prepared in the above (3), and the bag was sealed with a rubber string as shown in FIG. The heating pot was returned to the heating chamber and irradiated with 500 W microwaves. During the microwave irradiation, the bag expanded significantly, but steam gushed out from the outlet of the filter unit and the bag did not burst. Immediately after the microwave irradiation, the sample was taken out, and the temperature was measured immediately using a thermocouple (Digital Thermometer CT-700S, Custorn) to show 90. From this and the state of the contents at the time of irradiation, the internal temperature of the kettle had reached the range of 90 to 110 ° C. The volume of the sheet after removal was reduced to 33 OmL, and the volume was reduced to 1 Z5 compared to before the microwave treatment.
(5) 冷却後に加熱室から減容後のシーツを固体の塊として取り出し、 この固体物を焼却したところ、 必要とするエネルギーも少なく、 かつ有 害ガス等の問題も全くなかった。 (5) After cooling, the sheet after volume reduction was taken out of the heating chamber as a solid lump, and the solid was incinerated. The required energy was small, and there was no problem with harmful gases.
(6) —方、 マイクロ波の照射後、 加熱釜の内壁を滅菌水で濡らした滅 菌ガーゼで汚れを拭き取り、 日本薬局方の無菌試験法に準拠して、 この ガーゼをソィビーン ·カゼイン ·ダイジェスト ·寒天培地に接触させて、 該培地を 3 5 :のインキュベーターの中に 3 日間保管した後、 菌の増殖 の有無を目視観察したところ、 培地上には菌のコロニ一はほとんど観察 されなかった。 実施例 1 0 (6) — After microwave irradiation, the inside wall of the heating pot is wiped off with sterilizing gauze wetted with sterile water, and the gauze is soybean casein digest according to the sterility test method of the Japanese Pharmacopoeia. After contacting with the agar medium and storing the medium in a 35: 5 incubator for 3 days, the presence of bacterial growth was visually observed, and almost no bacterial colonies were observed on the medium. . Example 10
( 1 ) 循環器病棟より回収した、 実施例 9と同じ不織布シートを縫製し て作製された入院患者のおむつ 3枚と水 0. 7 k gを 2 0 Lの高密度ポ リエチレン袋に折りたたむことなく入れた。  (1) Without folding three inpatient diapers and 0.7 kg of water collected from the cardiology ward and sewn using the same nonwoven fabric sheet as in Example 9 in a 20-L high-density polyethylene bag I put it.
( 2 ) 上記 ( 1 ) の袋には孔径 0. 4 5 mのメンブランフィルターと 逆止弁を取付けた筒体からなる滅菌済みのフィルターュニッ トを取付け た後、 袋の口をビニールテープを用いて、 空気の漏れる部分がないよう にしつかりと縛って密閉した。  (2) After attaching a sterilized filter unit consisting of a cylinder with a 0.45 m pore size membrane and a check valve to the bag of (1) above, use a vinyl tape to seal the mouth of the bag. It was tightly tied and sealed so that there were no air leaks.
( 3 ) 実施例 9と同様にマイクロ波を照射したところ、 マイクロ波を照 射された袋の内容物は激しく膨張し、 多量の水蒸気がフィル夕一ュニッ 卜の出口より放出された。 マイクロ波照射後直ちに取り出し、 すぐに熱 電対 (C u s t om社、 デジタルサーモメーター C T— 7 0 0 S) で温 度を測定したところ、 9 0 を示した。 このこと及び照射時の内容物の 状態から釜の内部温度は 9 0〜 1 1 O t:の範囲に達していた。 また、 マ イク口波照射終了後、 内部の温度は急激に低下し、 袋はそれに伴って外 部の空気を吸入するようになるが、 短時間の内に逆止弁が働いて、 袋は 大気圧により圧迫されて減容化された。  (3) When irradiated with microwaves in the same manner as in Example 9, the contents of the bag irradiated with microwaves expanded violently, and a large amount of water vapor was released from the outlet of the filter unit. Immediately after the microwave irradiation, the sample was taken out, and the temperature was measured immediately using a thermocouple (Custom, digital thermometer CT-700S). From this and the state of the contents at the time of irradiation, the internal temperature of the kettle had reached the range of 90 to 11 Ot :. After the irradiation of the microphone, the temperature inside decreased sharply, and the bag began to take in the external air.However, the check valve was activated within a short time, The volume was reduced by being compressed by the atmospheric pressure.
( 4) その後、 加熱釜の内壁を滅菌水で濡らした滅菌ガーゼで汚れを拭 き取り、日本薬局方の無菌試験法に準拠して、このガーゼをソィビーン · カゼイン · ダイジェスト ·寒天培地に接触させて、 該培地を 3 5 °Cのィ ンキュベー夕一の中に 3日間保管した後、 菌の増殖の有無を目視観察し たところ、 培地上には菌のコロニーはほとんど観察されなかった。  (4) After that, wipe the inside wall of the heating pot with sterile gauze moistened with sterile water and contact the gauze with soybean, casein, digest, and agar medium in accordance with the sterility test method of the Japanese Pharmacopoeia. Then, after storing the medium in an incubator at 35 ° C for 3 days, the presence or absence of bacterial growth was visually observed, and almost no bacterial colonies were observed on the medium.
比較例 3 Comparative Example 3
( 1 ) 実施例 1 0 ( 1 ) と同様、 循環器病棟より入院患者の紙おむつ 3 枚と水 0. 7 k gを 2 0 Lの高密度ポリエチレン袋に折りたたむことな く入れ、 メンブランフィルターを装着せずに実施例 9と同様にマイクロ 波を照射したところ、 袋の内部の内容物は激しく膨張し、 多量の水蒸気 がフィルタ一なしの筒体の出口より放出され、 加熱釜の内壁に内容物の 飛沫の一部がこびりついた。 (1) As in Example 10 (1), put three disposable diapers and 0.7 kg of water from a cardiology ward into a 20-L high-density polyethylene bag without folding it, and attach a membrane filter. Without the same microscopy as in Example 9. When the waves were irradiated, the contents inside the bag expanded violently, and a large amount of water vapor was released from the outlet of the cylinder without a filter, and some of the droplets of the contents adhered to the inner wall of the heating pot.
( 2 ) マイクロ波の照射終了後、 袋は実施例 1 0と同様に大気圧により 圧縮されて減容化された。 その後、 加熱釜の内壁を滅菌水で濡らした滅 菌ガーゼをソィビーン · カゼィン · ダイジエスト ·寒天培地に接触させ て、 この培地を 3 5でのインキュベーターの中に 3 日間保管した後、 目 視観察したところ、 寒天培地上に多数のコロニーが観察され、 それらを 顕微鏡観察したところ、 寒天培地上に短径 1 . 1〜 1 . 、 長径 2 . 0〜 6 . 0 mの棒状の大腸菌や直径 1 z mの球状の黄色ブドウ球菌等 が多数観察された。 産業上の利用の可能性  (2) After the end of the microwave irradiation, the bag was compressed by atmospheric pressure to reduce the volume as in Example 10. Then, the sterilized gauze with the inner wall of the heating pot wet with sterile water was brought into contact with soybean, casein, digest, and agar medium, and this medium was stored in an incubator at 35 for 3 days and visually observed. However, when a large number of colonies were observed on the agar medium, and they were observed under a microscope, rod-shaped E. coli having a short diameter of 1.1 to 1.1 and a long diameter of 2.0 to 6.0 m and a diameter of 1 zm were observed on the agar medium. Numerous spherical Staphylococcus aureus were observed. Industrial applicability
本発明の減容化法及び装置は、 水の可塑効果を利用して親水性樹脂の 溶融温度を大幅に低下させるので、 従来の熱可塑性樹脂をそのまま溶融 するのに比較して、 減容化処理に必要な温度が低い分だけ簡単な装置を 用いて、 少ない電力使用量で実施することができ、 イニシャルコストと ランニングコス 卜の両面で大幅なコストダウンを達成することができる。 また、 減容化処理する際に本発明の収納袋を使用すれば、 感染性廃棄物 を袋の外に取り出したり、 袋の口を開いて何かをするような危険作業を 必要とせず、 どこでも誰にでも安全に簡単に廃棄物の減容化を図ること ができ、 しかもこの減容化後の廃棄物は消毒されており、 作業の安全性 はさらに高まる。 さらにまた、 上記の湿熱溶融状態の親水性樹脂を通常 のプラスチック製品に対するバインダ一として使用すると、 本発明は特 定の親水性樹脂成形物さえ使用しておれば、 通常のプラスチック製廃棄 物の混入を排除することなく、 減容化処理が可能であり、 感染性廃棄物 の処理に関わる容器費や運送費等の大幅な削減が可能である。 The volume reduction method and apparatus of the present invention greatly reduce the melting temperature of the hydrophilic resin by utilizing the plasticizing effect of water, so that the volume is reduced as compared to melting a conventional thermoplastic resin as it is. Since the temperature required for the treatment is low, the operation can be performed with a small amount of power using a simple device, and a significant cost reduction can be achieved in both initial costs and running costs. In addition, the use of the storage bag of the present invention during volume reduction processing does not require dangerous work such as taking out infectious waste out of the bag or opening the bag and doing something. Anybody can safely and easily reduce the volume of waste anywhere, and the waste after volume reduction has been disinfected, further improving work safety. Furthermore, when the above-mentioned hydrophilic resin in the wet-heat-melted state is used as a binder for ordinary plastic products, the present invention can be used as long as a specific hydrophilic resin molded product is used. Volume can be reduced without eliminating infectious waste It is possible to greatly reduce container costs, transportation costs, and the like related to the processing of refuse.

Claims

請求の範囲 The scope of the claims
I. 50°C以上の熱水又は水蒸気により溶融する親水性樹脂からなる樹脂成 形物を主体とする感染性医療廃棄物 (A) を水 (B) の存在下において、 70 〜1 50°Cの温度で処理することを特徴とする感染性医療廃棄物の減容化方法。 I. Infectious medical waste (A) mainly composed of a resin molded product made of hydrophilic resin that is melted by hot water or steam at 50 ° C or higher in the presence of water (B) at 70 to 150 ° A method for reducing the volume of infectious medical waste, comprising treating at a temperature of C.
2. 感染性医療廃棄物 (A) と水 (B) とを、 熱可塑性フィルムからなる収 納袋であって、 該袋本体の側面又は開口部に病原菌濾過手段が着脱可能又は着 脱不能の状態で備えられている収納袋に収納することを特徴とする請求項第 1 項に記載の減容化方法。  2. A storage bag made of a thermoplastic film, wherein the infectious medical waste (A) and the water (B) are provided with a removable or non-removable pathogen filtering means on the side or opening of the bag body. 2. The volume reducing method according to claim 1, wherein the storage bag is stored in a storage bag provided in a state.
3. 親水性樹脂がポリビニルアルコール系樹脂である請求の範囲第 1項また は第 2項に記載の減容化方法。  3. The method for reducing volume according to claim 1 or 2, wherein the hydrophilic resin is a polyvinyl alcohol-based resin.
4. 親水性樹脂が、 ポリビニルアルコールホモポリマ一である請求の範囲第 1〜 3項のいずれかに記載の減容化方法。  4. The volume reduction method according to any one of claims 1 to 3, wherein the hydrophilic resin is a polyvinyl alcohol homopolymer.
5. 親水性樹脂がエチレン共重合割合 1〜 24モル%のエチレンービニルァ ルコール共重合体である請求の範囲第 1〜 4項のいずれかに記載の減容化方法。  5. The volume reduction method according to any one of claims 1 to 4, wherein the hydrophilic resin is an ethylene-vinyl alcohol copolymer having an ethylene copolymerization ratio of 1 to 24 mol%.
6. 感染性医療廃棄物 (A) がポリビニルアルコール系樹脂からなる繊維製 品である請求の範囲第 1〜4項のいずれかに記載の減容化方法。  6. The volume reduction method according to any one of claims 1 to 4, wherein the infectious medical waste (A) is a fiber product made of a polyvinyl alcohol-based resin.
7. 繊維製品が、 不織布製品である請求の範囲第 1項に記載の減容化方法。  7. The volume reduction method according to claim 1, wherein the textile product is a nonwoven fabric product.
8. 収納袋を構成する熱可塑性フィルムが耐熱温度が 1 00°C以上の熱可塑 性ポリマーからなるフィルムである請求の範囲第 2項に記載の減容化方法。  8. The volume reduction method according to claim 2, wherein the thermoplastic film constituting the storage bag is a film made of a thermoplastic polymer having a heat resistance temperature of 100 ° C or more.
9. 病原菌濾過手段に逆止弁が備えられてなる請求の範囲第 2項に記 載の減容化方法。  9. The volume reduction method according to claim 2, wherein the pathogen filtering means is provided with a check valve.
1 0. 感染性医療廃棄物 (A) と水 (B) とを、 親水性樹脂以外の感 染性医療廃棄物の存在下で減容化させる請求の範囲第 1〜 9項のいずれ かに記載の減容化方法。  10. Any of claims 1 to 9, wherein the volume of the infectious medical waste (A) and the water (B) is reduced in the presence of infectious medical waste other than the hydrophilic resin. The volume reduction method described.
I I . 収納袋に感染性医療廃棄物を入れた後、 袋の中を減圧する請求 の範囲第 9項に記載の減容化方法。 II. After putting infectious medical waste in the storage bag, request to decompress the inside of the bag 10. The volume reduction method according to item 9 in the range.
1 2. 7 0〜 1 5 0 °Cの温度の処理を、 マイクロウエーブの照射によ り行う請求の範囲第 1〜 1 1項のいずれかに記載の減容化方法。  12. The volume reduction method according to any one of claims 1 to 11, wherein the treatment at a temperature of 12.70 to 150 ° C is performed by irradiation with a microwave.
1 3. 請求の範囲第 1〜 1 2項のいずれかに記載の減容化方法により 減容化された固形物を焼却することを特徴とする感染性医療廃棄物の廃 棄方法。  1 3. A method for discarding infectious medical waste, characterized by incinerating solid matter reduced in volume by the method for reducing volume according to any one of claims 1 to 12.
1 4. 5 0°C以上の熱水又は水蒸気により溶融する親水性樹脂からな る医療廃棄物を 7 0〜 1 5 0 °Cの温度で処理して該感染性医療廃棄物 (A) を減容化させるための装置であって、 筐体と、 加熱部と、 加熱手 段と熱の供給を制御する手段とからなる感染性医療廃棄物用減容装置。  14.5 Medical waste consisting of hydrophilic resin that melts with hot water or steam at 50 ° C or higher is treated at a temperature of 70 to 150 ° C to convert the infectious medical waste (A). A volume reduction device for infectious medical waste, comprising: a housing; a heating unit; a heating means and a means for controlling heat supply.
1 5. 加熱部が加熱室からなり、 該加熱室内に加熱釜を有する請求の 範囲第 1 4項に記載の装置。  15. The apparatus according to claim 14, wherein the heating section comprises a heating chamber, and the heating chamber has a heating pot.
1 6. 感染性医療廃棄物用減容装置から発生する電磁波の放散を防ぐ ための電磁波吸収機能あるいは電磁波遮蔽機能を付与した装置である請 求の範囲第 1 4項または第 1 5項に記載の装置。  1 6. Claims that are provided with an electromagnetic wave absorption function or an electromagnetic wave shielding function to prevent the emission of electromagnetic waves generated by the infectious medical waste volume reduction device. Equipment.
1 7. 加熱室内で発生する病原体を含む気体や臭気が減容装置の外に 漏出するのを防止する構造を有する請求の範囲第 1 4〜 1 6項のいずれ かに記載の装置。  1 7. The device according to any one of claims 14 to 16, having a structure for preventing gas or odor containing pathogens generated in the heating chamber from leaking out of the volume reduction device.
1 8. 加熱室内には、 加熱釜が着脱自在に載置され、 加熱釜を回転あ るいは振動させる手段を有する請求の範囲第 1 4〜 1 7項のいずれかに 記載の装置。  18. The apparatus according to any one of claims 14 to 17, wherein a heating pot is detachably mounted in the heating chamber, and the heating pot has means for rotating or vibrating the heating pot.
1 9. 加熱手段がマイク口ウエーブである請求の範囲第 1 4〜 1 8項 のいずれかに記載の装置。  1 9. The apparatus according to any one of claims 14 to 18, wherein the heating means is a microphone mouth wave.
2 0. 加熱釜内の親水性樹脂の温度又は液面を検出する手段を有する 請求の範囲第 1 4〜 1 9項のいずれかに記載の装置。  20. The apparatus according to any one of claims 14 to 19, further comprising means for detecting the temperature or the liquid level of the hydrophilic resin in the heating pot.
PCT/JP2002/006140 2001-06-26 2002-06-20 Method for processing easy-to-reduce resin molded article for infectious medical practice and its apparautus WO2003000167A1 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP2001-192246 2001-06-26
JP2001192246A JP2003002918A (en) 2001-06-26 2001-06-26 Easily volume-reducible resin composition for medical purpose
JP2001270232A JP2003073498A (en) 2001-09-06 2001-09-06 Disposal method of infectious medical waste and apparatus therefor
JP2001-270232 2001-09-06
JP2002-142272 2002-05-17
JP2002142272A JP2003325593A (en) 2002-05-17 2002-05-17 Housing bag for volume reduction of infectious medical waste

Publications (1)

Publication Number Publication Date
WO2003000167A1 true WO2003000167A1 (en) 2003-01-03

Family

ID=27347020

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2002/006140 WO2003000167A1 (en) 2001-06-26 2002-06-20 Method for processing easy-to-reduce resin molded article for infectious medical practice and its apparautus

Country Status (1)

Country Link
WO (1) WO2003000167A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014210520A1 (en) 2013-06-28 2014-12-31 Dynantis Corporation Secondary alkali metal/oxygen batteries
CN108861214A (en) * 2018-06-01 2018-11-23 嘉兴宇乾环保科技有限公司 A kind of smokeless dustbin of cell using the first dirty processing of electric energy

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54160094A (en) * 1978-06-07 1979-12-18 Eiken Chemical Filter seal for gas sterilization
JPH0412758A (en) * 1990-04-27 1992-01-17 Kawasaki Heavy Ind Ltd Method and device for processing medical treatment waste
US5181966A (en) * 1991-04-10 1993-01-26 Honeycutt Travis W Hot water soluble packaging materials
JPH0523657A (en) * 1991-07-18 1993-02-02 Kawasaki Heavy Ind Ltd Treating device for medical treatment waste
JPH0532301A (en) * 1991-07-30 1993-02-09 Japan Gore Tex Inc Waste storing body
JPH0557286A (en) * 1991-08-29 1993-03-09 Japan Steel Works Ltd:The Electromagnetic water treating device
US5339959A (en) * 1992-03-02 1994-08-23 Qci, Inc. Disposable medical waste bag
JP3052140B1 (en) * 1999-08-25 2000-06-12 新菱冷熱工業株式会社 Waste volume reduction equipment

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54160094A (en) * 1978-06-07 1979-12-18 Eiken Chemical Filter seal for gas sterilization
JPH0412758A (en) * 1990-04-27 1992-01-17 Kawasaki Heavy Ind Ltd Method and device for processing medical treatment waste
US5181966A (en) * 1991-04-10 1993-01-26 Honeycutt Travis W Hot water soluble packaging materials
JPH0523657A (en) * 1991-07-18 1993-02-02 Kawasaki Heavy Ind Ltd Treating device for medical treatment waste
JPH0532301A (en) * 1991-07-30 1993-02-09 Japan Gore Tex Inc Waste storing body
JPH0557286A (en) * 1991-08-29 1993-03-09 Japan Steel Works Ltd:The Electromagnetic water treating device
US5339959A (en) * 1992-03-02 1994-08-23 Qci, Inc. Disposable medical waste bag
JP3052140B1 (en) * 1999-08-25 2000-06-12 新菱冷熱工業株式会社 Waste volume reduction equipment

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014210520A1 (en) 2013-06-28 2014-12-31 Dynantis Corporation Secondary alkali metal/oxygen batteries
CN108861214A (en) * 2018-06-01 2018-11-23 嘉兴宇乾环保科技有限公司 A kind of smokeless dustbin of cell using the first dirty processing of electric energy
CN108861214B (en) * 2018-06-01 2021-02-19 嘉兴宇乾环保科技有限公司 Residential area smokeless garbage can for treating garbage by using electric energy

Similar Documents

Publication Publication Date Title
US5213758A (en) Method and apparatus for treating medical wastes
JP6069747B2 (en) Treatment method used for recycling absorbent hygiene products
US5124125A (en) Method for processing infectious waste using microwaves
RU2260444C2 (en) Disinfecting or sterilizing method
KR101775523B1 (en) Excretions diaper packaging apparatus having a deodorizing function
US5178828A (en) Apparatus for treatment of medical waste materials
KR20130059283A (en) Process for recycling absorbent sanitary products
US20030082966A1 (en) Superabsorbent disposable material
JP2013111575A (en) Apparatus and treatment method used for recycling absorbent sanitary products
WO2003000167A1 (en) Method for processing easy-to-reduce resin molded article for infectious medical practice and its apparautus
JP4606183B2 (en) Medical waste heat sterilizer
JP2003073498A (en) Disposal method of infectious medical waste and apparatus therefor
US20080044607A1 (en) Superabsorbent disposable material
CN116081084A (en) Anti-infection disposal bag with strong barrier property and moisture-proof bearing performance and application thereof
CA2058685A1 (en) Gelling material and gelling method
JP2003325593A (en) Housing bag for volume reduction of infectious medical waste
JP3238422B2 (en) Medical waste treatment method and apparatus
CN212424288U (en) Intelligent garbage bin of storage medical waste of area disinfection function
CN213084267U (en) Ventilative type biological safety sterilization disposal bag
CN111792245A (en) Intelligent garbage bin of storage medical waste of area disinfection function
RU2221592C2 (en) Method for disinfection of medical waste and device for its realization
CN215438085U (en) Waste collection device for nursing
JP2003002918A (en) Easily volume-reducible resin composition for medical purpose
KR102196616B1 (en) Reusing system and method of used disposable diapers
JP2004033387A (en) Easily volume-reducible medical plastic molded product

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU CA CN KR MX US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
122 Ep: pct application non-entry in european phase