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US3767362A - Sterilisation of materials - Google Patents

Sterilisation of materials
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US3767362A
US3767362AUS00150640AUS3767362DAUS3767362AUS 3767362 AUS3767362 AUS 3767362AUS 00150640 AUS00150640 AUS 00150640AUS 3767362D AUS3767362D AUS 3767362DAUS 3767362 AUS3767362 AUS 3767362A
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chamber
gaseous
sterilising agent
treatment chamber
sterilising
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M Griffin
B King
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Gardeners of Gloucester Ltd
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Abstract

A method of sterilising powders and other fine-grained pulverulent or granular materials employs a gaseous sterilising agent. An upwardly extending closed treatment chamber is partially filled with the material to be sterilised, and the gaseous sterilising agent is admitted to the lower end of the chamber in such manner that the material is flung upwardly into free space at the top of the chamber and substantially allowed to settle again whereafter the process is repeated. Thus, the material is displaced by the sterilising agent and allowed to settle and stand again, or at any rate to complete its settling movement at least to a fluid state, several times. The sterilising agent escapes from an outlet at the top of the chamber, and it is desirably admitted to the latter in a series of pressure shocks of short duration, and in such manner that the material is whirled upwardly by the shock pulses in an ascending peripheral vortex so that the particles are in a state of suspension from which they fall downwards again in an inner vortex axially of the chamber.

Description

[ STERlLlSATlON OF MATERIALS Inventors: Michael John Griffin, Hucclecote,
Gloucester; Brian Clarence King, Gloucester, both of England [73] Assignee: Gardeners of Gloucester Limited,
Gloucester, England [22] Filed: June 7, 1971 [21] A pl. No.: 150,640
[30] Foreign Application Priority Data June 10, 1970 Great Britain 28,010/70 [52] US. Cl 21/58, 21/57, 21/D1G. 4 [51] Int. Cl. A611 1/00, A611 13/00 [58] Field of Search 2l/D1G. 4, 56, 58,
[56] References Cited UNITED STATES PATENTS 3,068,064 12/1962 McDonald 21/D1G. 4 3,069,734 12/1962 Leuthner 21/D1G. 4 3,088,179 5/1963 Leuthner.. 21/D1G. 4 3,341,280 9/1967 Eolkin 21/D1G. 4 3,341,335 9/1967 Eolkin et al. 21/58 X 3,477,807 11/1969 Ernst 2l/D1G. 4 3,600,127 8/1971 Kereluk et a1... 21/58 3,407,029 10/1968 Krahe 21/56 X Great Britain 2l/D1G. 4
993,757 6/1965 Great Britain 2l/D1G. 4
Primary Examiner-*Barry S. Richman Attorney-Young & Thompson 57 ABSTRACT A method of sterilising powders and other fine-grained pulverulent or granular materials employs a gaseous sterilising agent. An upwardly extending closed treatment chamber is partially filled with the material to be sterilised, and the gaseous sterilising agent is admitted to the lower end of the chamber in such manner that the material is flung upwardly into free space at the top of the chamber and substantially allowed to settle again whereafter the process is repeated. Thus, the material is displaced by the sterilising agent and allowed to settle and stand again, or at any rate to complete its settling movement at least to a fluid state, sev- 6 Claims, 3 Drawing Figures PATENIEUnmza ma SHEEI10F 3 6km Cums/v05 k/A a INVENTORS 8%"? M ATTORNEYS PATENTED UN 2 3 I973 SHEET 2 OF 3 STERILISATION OF MATERIALS This invention relates to the sterilisation of materials, for example powders and other fine-grained pulverulent and granular materials, that is to say the treatment of such materials with gaseous sterilising agents with a view to destroying or preventing bacterial growths or the like.
Hitherto, such sterilisation has been carried out, gen erally speaking, with the materials in the prepacked state, for example in sealed plastic bags, or with the material exposed in shallow layers on open trays, in a sealed chamber or vault. This method of procedure requires long exposure times, for example of the order of 16 to 48 hours, with the attendant risk of degradation of the product by the gaseous sterilising agent. It has, however, been proposed to sterilise material in bulk by passing the gaseous sterilising agent through a body of the material in a tumbling-type unit which assists in obtaining intimate contact between the gaseous sterilising agent and the particles of powder. Even so, the sterilising time required may be of the order of 4 hours.
More recently it has been proposed to effect bulk sterilisation of powders by separating the particles of the powder in a stream of the gaseous sterilising agent which fluidises a bed of the powder to be sterilised. With that process the treatment time is claimed to have been reduced to between 5 and 20 minutes duration with the gaseous sterilising agent streaming continuously during that period.
The main object of the present invention is to provide improvements in the sterilisation of powders and other fine-grained pulverulent or granular materials which enables the materials to be sterilisedin bulk in a reasonably short period of time depending on circumstances while using minimal quantities of the gaseous sterilising agent and ensuring complete removal of the gas from-the product, thereby avoiding all possibility of degradation of the latter.
According to the invention a method of sterilising powders and other fine-grained pulverulent or granular materials comprises, partially filling an upwardly extending closed treatment chamber with the material, admitting a gaseous sterilising agent to the lower end of the treatment chamber in such manner that the mate-- rial is flung upwardly into the free space'at the top of the chamber and substantially allowed to settle again whereafter the process is repeated, the gaseous sterilising agent escaping from an outlet at the top of the chamber. I
Thus, the material is displaced and allowed to settle and stand again, or at any rate to complete its settling movement at least to a fluid state, several times by the gaseous sterilising agent as compared with the fluidisingof a bed of material by a continuous stream of the gaseous sterilising agent previously proposed.
If desired the gaseous sterilising agent may be admitted in a series of pressure shocks of short duration and at such pressure that the foregoing effect is achieved. Preferably the manner of admission of the gaseous sterilising agent to the treatment chamber and the form of the latter are such that the material is whirled upwardly. by the shock pulses of the pressurised gaseous sterilising. agent in an ascending peripheral vortex so that the particles are in a state of suspension from which'they fall downwards again in an inner vortex axially of the chamber The gaseous sterilising agent may be one which destroys by chemical action the bacteria and/or other organisms in respect of which sterility is to be achieved. Ethylene oxide, either alone or in a carrier gas such as nitrogen, and formaldehyde are examples. Preferably the sterilisation is carried out with control of the material and gas temperatures, humidity and pressure. For example in a typical case a temperature of around 122F and a relative humidity of about 45 percent to 5 0 percent may be established in the treatment chamber.
The invention also covers apparatus for carrying the foregoing method steps into effect. For the admission of the gaseous sterilising agent to the treatment chamber in the aforesaid series of pressure shocks of short duration a plurality, preferably a multiplicity, of separate nozzles are provided at the lower end of the treatment chamber and to and from which the pressurised gaseous sterilising agent is intermittently fed and cut off under the control of a timing device. Preferably the nozzles are arranged in a ring at equiangular separation around a frusto-conical lower end wall of the treatment chamber, the axes of the nozzles being parallel to the frusto-conical wall but slanted in order to impart the aforesaid whirling motion to the gaseous sterilising agent.
By way of example, the application of the invention to the sterilisation of talc will now be described with reference to the accompanying drawings, inwhich:
FIG. 1 is a flow diagram illustrating one typical arrangement of the tale sterilising plant,
FIG. 2 is a similar view of an alternative exemplary sterilising plant, and 7 FIG. 3 is a flow diagram illustrating a sterilising gas supply rig, suitable for use with either of the foregoing plants but shown more particularly as associated with that of FIG. 1.
The talc is initially ground to a fine impalpable powder in which state it is stored in alarge silo 11. From the bottom of thesilo 11 the powder is removed by means of a discharge worm 12 to the lower end of apneumatic elevator 13 from the upper end of which it is delivered, in the plant of FIG. 1, to duplex powder heaters 14' andlS, which may be steam or oil jacketed chambers, in which the powder is preheated to a temperature of [00F to 180F, for example 140F. From theheaters 14 and 15 the talc is fed into asingle sterilising chamber 16, the feed means being such that thechamber 16 is filled to an extent of approximately 60 percent of its capacity.
Thesterilising chamber 16 is substantially cylindrical in shape with its axis vertical and has a frusto-conical lower end or base 16a.- At its upper end the sterilising chamber has a gas outlet 17 (see FIG. 3) embodying filtering means. The opening of the frusto-conical base of the sterilising chamber is closed by an upwardlyc'oned element 18 which serves to deflect the material within the chamber to the outer periphery of thefrustoconical base 16a of the latter and is capable of being raised to provide an annular opening through which material may be discharged through ashort outlet pipe 19. Surrounding the base of theconed element 18 is a ring main 20 having a series of equiangularly separated nozzles (not shown) leading therefrom and opening on to the lower wall of the frusto-conical base' 16a of the sterilising chamber.
To the ring main 20 through an admission conduit 22 a 10 percent ethylene oxide and percent nitrogen mixture is fed. From the ring main 20 the gas mixture passes through a multiplicity of radially directed bores each of which leads to one of the aforesaid nozzles. There may be, for example, ten such bores and nozzles at equiangular separation around the frusto-conical base 16a of thechamber 16. The nozzles may be of Laval type arranged with their axes parallel to the frusto-conical bottom portion of the sterilising chamber but slanted so that the separate jets of gas mixture issue therefrom with an upwardly directed circulatory movement.
Entry of the gas mixture to the ring main 20 occurs through the intermediary of acontrol valve 23 which operates as a timing device. As a result, powerful but very brief shocks of pressure gas issue from the nozzles in a circular movement in order to whirl the talc freely upwards within thechamber 16 until it is in a state of suspension, the pressure gas shocks following one another only at such time intervals that the talc can settle again between each two pressure shocks at least to a fluid state. Usually the talc is allowed to settle and stand for some minutes to allow the chemical sterilising action to proceed before the next pressure shock. The upward whirling movement of the talc takes place in the vicinity of the cylindrical wall of thesterilising chamber 16 into the free space at the top of the latter where the tale is in a state of suspension and whence it falls spirally near the centre of the chamber at the termination of each blast which is of only a few seconds duration. On falling to the bottom of the chamber the talc is deflected by the central upwardlyconed element 18 towards the peripheral wall of the frusto-conical base 16a and then whirled upwardly again by the next succeeding blast from the nozzles.
After the foregoing procedure has been repeated several times thecone 18 is raised penumatically to allow the sterilised talc to be discharged through the annular opening already mentioned and theoutlet pipe 19 into abuffer hopper 24 from the lower end of which it is discharged by a worm through arotary seal 26 and pneumatically conveyed along aduct 27 to a storage silo (not shown). The treatment time may be, for example, of the order of l to 3 hours.
Referring now more particularly to FIG. 3, acylinder 28 of ethylene oxide is pressurised from acylinder 29 of nitrogen, thereby delivering the ethylene oxide through a flow-control valve 30 to a heating and humidifyingreservoir 32. A bank ofnitrogen cylinders 33 also deliver to thereservoir 32 through pressure and flow-control valves 34 and 35, the flows from thevalves 30 and 35 joining at the region of an inlet/outlet pipe 36 of the reservoir. I
The reservoir is heated by anelectrical heating jacket 37, which is thermostatically controlled, and the internal reservoir gas temperature is monitored by apyrometric sensing element 38 connectable to atemperature indicator 39. Theindicator 39 is alternatively connectable to apyrometric sensing element 40 in thechamber 16, whereby to monitor the treatment temperature. Thepipe 36 is jacketed to prevent undue heat loss and supplies thevalve 23 through flow andpressure control valves 42 and 43.
Apressure gauge 44 monitors the internal reservoir pressure, and humidifying steam is admitted through a flow-control valve 45. Ahygrometer indicator 46 is alternatively connectable to a humidity sensinghead 47 in thereservoir 32 and asimilar head 48 in thetreatment chamber 16. This enables the steam flow to be controlled to maintain appropriate humidity in the treatment zone, and thereservoir 32 is also fitted with adrain valve 49.
A source of compressed air can be connected to the described heating and humidifying means through a flow-control valve 50 connected to thereservoir 32. Thus by appropriate operation of the various flowcontrol valves compressed air may be admitted to the treatment chamber for a cleaning run, and through the various pipe-lines for purging purposes.
The alternative arrangement of the talc sterilising plant of FIG. 2 enables continuous preheating of the talc to be carried out notwithstanding the batch sterilisation and discharge of the tale from the sterilisingchamber 16 in the manner already described. This is achieved by delivering the powder from the upper end of thepneumatic elevator 13 to a battery of, for example five as shown, continuous powder heaters 52 arranged in cascade. From the lowermost powder heater 52 the talc passes through arotary seal 53 to apneumatic conveyor 54 along which air is blown by a blower 55, this air being heated in aheat exchanger 56 in order to avoid chilling of the preheated talc. Thepneumatic conveyor 54 feeds the preheated tale to one or other of two sterilisingchambers 16 of the construction already described and arranged in parallel so that one of the chambers is being filled while powder is undergoing sterilisation in the other. Thelatter chamber 16 is then discharged and refilled while the talc in the first chamber is undergoing the sterilisation treatment.
The gas mixture is passed through heating and humidifying means as before but passes thence to a selector valve 57 which determines which of the two sterilisingchambers 16 it enters by way ofrespective admission conduits 58,59. It will be understood that the selector valve 57 operates in timed relation to avalve 60 which determines which of the sterilisingchambers 16 is being filled at a given time. From the bottoms of the sterilising chambers the sterilised powder passes through respective short outlet pipes into acommon pipe 19 leading to abuffer hopper 24 as already described.
A pneumatictimer control unit 62, shown in FIG. 3, controls thevalve 23 of eachchamber 16 so that the gaseous sterilising agent is admitted to thechambers 16 in the described pulsed manner. In either plant thestorage silo 11 may be replaced by an automatic bag opener to which the talc is brought by way of a'bag conveyor and whence the material is fed into a transfer hopper, this modification not being shown in the drawings. The transfer hopper would then deliver to the discharge worm 12 of the plants as illustrated.
To provide even distribution of the tale in the or eachchamber 16, the latter may include at the top end a rotary discharge spreader of generally volute form on to which the talc is delivered. From this spreader the talc is then distributed so that it delivers into the chamber in the form of an even curtain.
We claim:
1. A method of sterilising powders and other finegrained pulverulent or granular materials comprising partially filling an upwardly extending closed treatment chamber with the material, admitting a gaseous sterilising agent to the lower end of the treatment chamber at a flow rate in excess of that required to fluidize said material and in such manner that the material is flung upwardly into the free space at the top of the chamber while the gaseous sterilising agent escapes from an outlet at the top of the chamber, and then discontinuing the flow of said gaseous sterilizing agent into said treatment chamber whereby said material is allowed to settle whereafter further gaseous sterilising agent is admitted to repeat said flinging and settling procedure.
2. A method according toclaim 1, wherein the gaseous sterilising agent is admitted in a series of pressure shocks of short duration.
3. A method according toclaim 1, which includes pre-heating the material prior to delivery thereof to the treatment chamber and effecting controlled heating and humidifaction of the gaseous sterilising agent prior to admission thereof to the treatment chamber, said heating and humidification being carried out in a reservoir which contains thermostatically controlled electrical heating means and to which steam is fed 4. A method of sterilising powders and other finegrained pulverulent or granular materials comprising partially filling an upwardly extending closed treatment chamber with the material, admitting a gaseous sterilising agent to the lower end of the treatment chamber at a flow rate in excess of that required to fluidize said material and in such manner that the material is whirled upwardly by the gaseous sterilising agent in an ascending peripheral vortex from which the particles of said material fall downwards in an inner vortex axially of the chamber upon termination of the flow of said gaseous sterilising agent, the gaseous sterilising agent being allowed to escape from an outlet at the top of the chamber discontinuing the flow of said gaseous sterilizing agent into said treatment chamber until settling of said material is substantially complete and admitting further gaseous sterilising agent into said treatment chamber to repeat said whirling and falling procedure when settling of the material is substantially complete.
5. A method according to claim 4, which includes effecting controlled heating and humidification of the gaseous sterilising agent prior to admission thereof to the treatment chamber.
6. A method according to claim 4, which includes pre-heating the material prior to delivery thereof to the treatment chamber.

Claims (5)

  1. 4. A method of sterilising powders and other fine-grained pulverulent or granular materials comprising partially filling an upwardly extending closed treatment chamber with the material, admitting a gaseous sterilising agent to the lower end of the treatment chamber at a flow rate in excess of that required to fluidize said material and in such manner that the material is whirled upwardly by the gaseous sterilising agent in an ascending peripheral vortex from which the particles of said material fall downwards in an inner vortex axially of the chamber upon termination of the flow of said gaseous sterilising agent, the gaseous sterilising agent being allowed to escape from an outlet at the top of the chamber discontinuing the flow of said gaseous sterilizing agent into said treatment chamber until settling of said material is substantially complete and admitting further gaseous sterilising agent into said treatment chamber to repeat said whirling and falling procedure when settling of the material is substantially complete.
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Cited By (25)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3897210A (en)*1971-05-071975-07-29Bacfree Ind IncMethod and apparatus for sterilizing particulate material
US3994685A (en)*1974-05-111976-11-30Loedige WilhelmApparatus for sterilizing loose material
FR2331355A1 (en)*1975-11-141977-06-10Boots Co Ltd PROCESS FOR STERILIZING A POWDER AND INSTALLATION FOR ITS USE
US4062646A (en)*1974-05-111977-12-13Loedige WilhelmProcess for sterilizing loose material
US4062982A (en)*1975-05-281977-12-13General Foods, LimitedMethod for sterilization of food products
US4130393A (en)*1977-06-241978-12-19Colgate-Palmolive CompanyMethod for sterilizing with and recycling of ethylene oxide
US4250143A (en)*1979-06-081981-02-10The United States Of America As Represented By The Administrator Of The National Aeronautics And Space AdministrationSystem for sterilizing objects
US4889708A (en)*1985-06-271989-12-26The Boc Group, Inc.Fumigant system
US4921674A (en)*1988-09-061990-05-01Enos Quentin MGravity feed apparatus and method for fumigation, detoxification and nutrification of plant seed
US5360593A (en)*1987-12-291994-11-01Alcon Laboratories, Inc.Heat sterilization of labile antibiotics
US5422074A (en)*1991-10-311995-06-06Envirotrust Technologies, Inc.Methods for treating infectious wastes
US5464580A (en)*1994-06-011995-11-07Ethicon, Inc.Process of sterilization
US20060185189A1 (en)*2003-11-132006-08-24Airex Co., Ltd.Method of decontamination and decontamination apparatus
US20070274858A1 (en)*2006-02-252007-11-29Childers James A Method and system for conducting vapor phase decontamination of sealable entities and their contents
US20080080999A1 (en)*2006-09-292008-04-03Bondar Douglas ESystem and method for recycling sterilant gas
US20090148492A1 (en)*2007-10-312009-06-11Vipul Bhupendra DaveMethod of making a vascular closure device
US20100078336A1 (en)*2002-10-042010-04-01Ethicon, Inc.Packaged antimicrobial medical device and method of preparing same
WO2011008547A1 (en)2009-06-292011-01-20Ethicon. Inc.Packaged antimicrobial medical device having improved shelf life and method of preparing same
US20110076312A1 (en)*2009-09-292011-03-31Ethicon, Inc.Antimicrobial/antibacterial medical devices coated with traditional chinese medicines
US8268238B2 (en)2006-09-292012-09-18Tyco Healthcare Group LpSystem and method for recycling sterilant gas
WO2013152271A1 (en)2012-04-062013-10-10Ethicon, Inc.Packaged antimicrobial medical device having improved shelf life and method of preparing same
US8668867B2 (en)2002-10-042014-03-11Ethicon, Inc.Method of preparing an antimicrobial packaged medical device
US9149273B2 (en)2002-10-042015-10-06Ethicon, Inc.Packaged antimicrobial medical device
US9474524B2 (en)2002-10-042016-10-25Ethicon, Inc.Packaged antimicrobial medical device having improved shelf life and method of preparing same
WO2023209629A1 (en)2022-04-292023-11-02Ethicon, Inc.Sutures with expanded antibacterial properties

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Cited By (41)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3897210A (en)*1971-05-071975-07-29Bacfree Ind IncMethod and apparatus for sterilizing particulate material
US3994685A (en)*1974-05-111976-11-30Loedige WilhelmApparatus for sterilizing loose material
US4062646A (en)*1974-05-111977-12-13Loedige WilhelmProcess for sterilizing loose material
US4062982A (en)*1975-05-281977-12-13General Foods, LimitedMethod for sterilization of food products
FR2331355A1 (en)*1975-11-141977-06-10Boots Co Ltd PROCESS FOR STERILIZING A POWDER AND INSTALLATION FOR ITS USE
US4130393A (en)*1977-06-241978-12-19Colgate-Palmolive CompanyMethod for sterilizing with and recycling of ethylene oxide
US4250143A (en)*1979-06-081981-02-10The United States Of America As Represented By The Administrator Of The National Aeronautics And Space AdministrationSystem for sterilizing objects
US4889708A (en)*1985-06-271989-12-26The Boc Group, Inc.Fumigant system
US5360593A (en)*1987-12-291994-11-01Alcon Laboratories, Inc.Heat sterilization of labile antibiotics
US4921674A (en)*1988-09-061990-05-01Enos Quentin MGravity feed apparatus and method for fumigation, detoxification and nutrification of plant seed
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US5464580A (en)*1994-06-011995-11-07Ethicon, Inc.Process of sterilization
EP0685399A1 (en)1994-06-011995-12-06Ethicon, Inc.Process of sterilization
US20100078336A1 (en)*2002-10-042010-04-01Ethicon, Inc.Packaged antimicrobial medical device and method of preparing same
US9149273B2 (en)2002-10-042015-10-06Ethicon, Inc.Packaged antimicrobial medical device
US8668867B2 (en)2002-10-042014-03-11Ethicon, Inc.Method of preparing an antimicrobial packaged medical device
US8960422B2 (en)2002-10-042015-02-24Ethicon, Inc.Packaged antimicrobial medical device and method of preparing same
US9597072B2 (en)2002-10-042017-03-21Ethicon, Inc.Method of preparing a packaged antimicrobial medical device
US9597067B2 (en)2002-10-042017-03-21Ethicon, Inc.Packaged antimicrobial medical device and method of preparing same
US9474524B2 (en)2002-10-042016-10-25Ethicon, Inc.Packaged antimicrobial medical device having improved shelf life and method of preparing same
US20060185189A1 (en)*2003-11-132006-08-24Airex Co., Ltd.Method of decontamination and decontamination apparatus
US7146746B2 (en)*2003-11-132006-12-12Airex Co., Ltd.Method of decontamination and decontamination apparatus
US8236240B2 (en)*2006-02-252012-08-07James Arthur ChildersMethod and system for conducting vapor phase decontamination of sealable entities and their contents
US20070274858A1 (en)*2006-02-252007-11-29Childers James A Method and system for conducting vapor phase decontamination of sealable entities and their contents
US7666369B2 (en)2006-09-292010-02-23Tyco Healthcare Group LpSystem and method for recycling sterilant gas
US7910055B2 (en)2006-09-292011-03-22Tyco Healthcare Group LpMethod for recycling sterilant gas
US20080080999A1 (en)*2006-09-292008-04-03Bondar Douglas ESystem and method for recycling sterilant gas
US8268238B2 (en)2006-09-292012-09-18Tyco Healthcare Group LpSystem and method for recycling sterilant gas
US8685336B2 (en)2006-09-292014-04-01Covidien LpSystem and method for recycling sterilant gas
US9044531B2 (en)2007-10-312015-06-02Cordis CorporationVascular closure device
US8790684B2 (en)2007-10-312014-07-29Cordis CorporationVascular closure device
US8980299B2 (en)2007-10-312015-03-17Cordis CorporationMethod of making a vascular closure device
US20090171388A1 (en)*2007-10-312009-07-02Vipul Bhupendra DaveVascular closure device
US20090148492A1 (en)*2007-10-312009-06-11Vipul Bhupendra DaveMethod of making a vascular closure device
WO2011008547A1 (en)2009-06-292011-01-20Ethicon. Inc.Packaged antimicrobial medical device having improved shelf life and method of preparing same
US20110076312A1 (en)*2009-09-292011-03-31Ethicon, Inc.Antimicrobial/antibacterial medical devices coated with traditional chinese medicines
EP3409302A1 (en)2009-09-292018-12-05Ethicon, Inc.Antimicrobial/antibacterial medical devices coated with traditional chinese medicines
WO2013152271A1 (en)2012-04-062013-10-10Ethicon, Inc.Packaged antimicrobial medical device having improved shelf life and method of preparing same
US10245025B2 (en)2012-04-062019-04-02Ethicon, Inc.Packaged antimicrobial medical device having improved shelf life and method of preparing same
US11707272B2 (en)2012-04-062023-07-25Cilag Gmbh InternationalPackaged antimicrobial medical device having improved shelf life and method of preparing same
WO2023209629A1 (en)2022-04-292023-11-02Ethicon, Inc.Sutures with expanded antibacterial properties

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GB1335557A (en)1973-10-31
DE2128805A1 (en)1971-12-16
DE2128805B2 (en)1977-04-21

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