CN106421864A - Improved method and improved equipment for generating high disinfection effect in air and surface - Google Patents
Improved method and improved equipment for generating high disinfection effect in air and surface Download PDFInfo
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- CN106421864A CN106421864A CN201610205954.5A CN201610205954A CN106421864A CN 106421864 A CN106421864 A CN 106421864A CN 201610205954 A CN201610205954 A CN 201610205954A CN 106421864 A CN106421864 A CN 106421864A
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/16—Disinfection, sterilisation or deodorisation of air using physical phenomena
- A61L9/18—Radiation
- A61L9/20—Ultraviolet radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/02—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
- A61L2/08—Radiation
- A61L2/10—Ultraviolet radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/10—Apparatus features
- A61L2202/11—Apparatus for generating biocidal substances, e.g. vaporisers, UV lamps
Landscapes
- Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
Abstract
The present invention relates to an improved method, an improved process and improved equipment for disinfecting and sterilizing all types of surfaces, indoor air and side-room air contaminated by microorganisms, wherein the improved equipment comprises a multi-wavelength narrow-spectral width UV source, and provides good effects in damage on viruses, bacteria, the DNA of spores and cysts, and shells or membranes compared to the mercury-based 254 nm sterilizing lamp.
Description
The application is filing date on January 29th, 2009, Application No. is the 200980155935.4th, invention entitled " is used for
The divisional application of the Chinese patent application of the method and apparatus of the improvement of generation high level disinfection effect in air and surface ".
Technical field
Present invention teaches for air, all types of surface and food are carried out except microbial decontamination and sterilizing change
Kind method and apparatus.Described method utilizes the multi-wavelength UV photon being combined with remote UV photon and the effect of UV-C photon, thus
Produce higher than be used alone arbitrary source and the disinfective action of issuable disinfective action level.Described equipment is by phase
Two room compositions separately of different wave length are produced during with excitation process.
Background technology
It is based primarily upon use commercially available sterilization ultraviolet (GUV) for the sterilizing of air and all prior aries of sterilization
Lamp.These lamps are pulse excitation or continuous agitation.Continuous lamp is based on mercury, and mainly launches at 254nm.Have at present
A lot of companies produce the equipment based on GUV light for destroying virus in room air, bacterium, spore and pathogen.Because
It makes Interior Space air-flow Ricoh of the place of being constantly exposed to and has enough process open-assembly times in time in the past, therefore has
The process of effect.Required open-assembly time, this depended on different microorganisms under 254nm in the range of extremely hundreds of seconds tens of seconds
Light absorpting ability.Although the room air in this independent room for process is effective, but for process quickly through big pipeline
Large volume moving air impracticable.The needing of its long process time makes it in processing most of surface and impracticable.
According to its not same-action to biosystem, wide UV spectrum is divided into four regions.Doctor about these regions
Technics mainly has:UV-A, its scope being defined as 320nm to 400nm or wave band;UV-B, it is defined as 280nm to 320nm
Wave band;And UV-C, it is defined as comprising the wavelength less than 280nm.At present, UV-C wave band be further divided into by 185 to
Two parts of the UV-C composition of the remote UV (FUV) of 250nm and 250 to 290nm.Because the absorption spectrum of chemical bond is wider than these
The wave band of justice definition is much narrower, and therefore photochemical scholar and photobiologist typically do not use these terms.As an alternative, it uses
The wavelength of the radiation applied is to be associated with viewed effect.
Advocate that UV-C (GUV) radiation using sterilization makes DNA inactivate.This is because mercury lamp is close in the transmitting of 254nm
In good DNA absorption bands.Not yet advocate to be combined to produce higher levels of microorganism deactivated by the UV photon of different wave length.
Additionally, not yet advocate to be combined to produce higher levels of microorganism deactivated by FUV photon and UV-C photon.Remote UV photon source targeting
Peak absorbs the nitrogenous base absorption bands at 200nm, and UV-C photon source targets other nitrogenous base absworption peaks (282nm) and ammonia
Base acid absworption peak (254-265nm).Be used alone compared with arbitrary photon source, applying of multi-wavelength UV photon is killed in cause of disease
Or inactivation aspect creates improvement.
In the several years in past, become commercially available based on the new UV emitting lamps exciting of excimers.These
Transmitter produces single line or narrow spectrum is launched, and it is launched wavelength and is formed decision by the gas of lamp.If selection process lamp wavelength with
The absworption peak of close match microorganism different component absorption bands, then can be delivered to micro-in the short period of time by lethal dose
Biological.Do not find any patent instruct use have support device with united FUV source, UV-C source, it can effectively and have
Efficient the air of the large volume in each preparatory phase, big surface and little surface and food are carried out disinfection and sterilize.
In this manual, sterilization functions or sterilizing refers to that sterilization functions or the high level disinfection being defined by US FDA are made
With.Disinfectant or disinfective action refer to the disinfective action of every other level.
The genomic constitution of all viable biological is included in its DNA molecular.Replicate and sent out by the division of DNA molecular
Raw, and DNA molecular replicates itself by the conversion of its structure.The each several part of DNA molecular has been named as such as pyrimidine base
Base, cytimidine, thymidine or uracil, it forms the one group of biochemicals sustaining life.Length dna molecule by use with
See similar simple connection of those in sugar and keep together.
Researcher thinks that the energy of GUV photon causes producing between specific biochemicals the shape of strong (covalency) key
Become.But, the bond strength of covalent bond is highly dependent on the relative position participating in atom.Bilateral symmetry when key hydrogen atom in key
When, call it as dimer.Dimer is very strong key, and generally will not rupture during liquid gasification.Known GUV light
Produce thymine dimer, cytimidine-thymine dimer and cytosine dimers.After forming dimer, DNA enters
The duplication of one step stops.Fig. 1 shows and forms dimeric principle in DNA molecular.
DNA molecular absorbs from about 180nm to the light of about 400nm.Use the commercial sterilization lamp exciting based on mercury, this is because
Its photon sending is close to the 260nm absworption peak of DNA amino acid.Mercury gas in lamp and pressure thereof determine the ripple launching light
Long.For low pressure (LP) and low pressure high output (LPHO) lamp, a length of 254nm of transmitted wave.For middle pressure lamp, transmitting boundary is
200nm is to higher than 400nm.But, for continuous emission lamp, the emitted luminescence intensity less than 245nm is invalid;And for middle pressure
Lamp, the emitted luminescence intensity less than 235nm is invalid.Xenon in flashlight produces the multi-wavelength similar with medium pressure mercury lamp and sends out
Penetrate.But, to this patent it is essential that amultiwavelength source produces two different narrow spectrum widths (commonly referred to as single line) transmittings, its
At least two peak corresponding to microbial DNA absorbs chromophore.In other parts of this patent, this source is referred to as double-single line lamp.See
Report in document is proved the UV photon of other wavelength or low wavelength blue light can promote the reparation of impaired key, and allows biology
Restart duplication.This is often referred to as photoreactivation.
DNA action spectrum shows multiple peak, and it depends on the composition of the nitrogenous base constituting described biology and amino acid.Although
Shown that FUV photon is effective for breaking bonds, but the appropriate dual wavelength combination of FUV and UV-C may equally effectively or more added with
Effect.
Recent technical papers (Peak etc., UV action spectra for DNAdimmer induction.,
Photochemistry and Photobiology, 40,5 (613-620), 1984) show that dimeric formation is not to make DNA
The sole requirement of inactivation.The suction to different wave length photon for the different molecular group (molecular group) in length dna molecule
Receive the energy transfer that will strengthen between group.Compared with the single band photon only affecting minority group, damage or destroy these key bases
Group can more effectively make DNA inactivate.Still nobody completes the detailed of the inactivation efficacy of the different single line UV transmitters to work in combination
Thin research.
A lot of document is had to relate to the multi-photon effect to material, owing to the energy of different photons can resonate or at the electricity of molecule
Producing different energy levels in son or atom, it can produce different processes.Principle in this specification is to use by identical
The multiple narrow line wavelength that lamp sends produces multiple absorption features effect to microorganism.It is believed that due to multi-Photon Interaction
Its destruction can be played by more approach, therefore can produce bigger infringement and higher survival rate declines.These
Approach can occur simply by the RESONANCE ABSORPTION causing the physical rupture of key in approach.It also results in different aminoacids, contains
The significant cross linking of other crucial keys of nitrogen base, nucleotides and permission bioautography.The crosslinking of these keys can and can cause
Make the condition that biology cannot replicate further, and the propagation of crowd in this region for these infectious substances can be reduced.
The energy of the photon launched is determined by its wavelength.Photon energy is about 5ev under 250nm, and at shorter ripple
Long lower increase.Photon by different-energy is affected by the different keys in DNA.
Nitrogenous base in a lot of peptide bonds and DNA in 540kJ/ mole of photon energy of FUV lamp is beyond protein
Bond energy.Bacterial cell is comprised lipid film or the cell membrane cincture of a lot of protein molecular.Cell membrane is for the life of a lot of bacteriums
Deposit most important.FUV light can damage the albumen in this structure, and GUV then can not.This can cause the physical hazard of microorganism.
Fig. 2 shows microphoto under 1000x magnifying power for the atrophy bacillus (Bacillus atrophaeus).At 1000x mirror
Head lower it may be clearly seen that, photon impact causes sidewall rupture and biological division.This is that known photon causes really to cause of disease
Infringement and the first photographic evidence destroying.The corresponding carriers piece accepting identical radiant exposure does not produce any duplication, and it is right to show
Biological 100% is killed.
Fully prove, in all albumen, peptide bond be cause two different wavelength regions (i.e. at 200nm and
At 280nm) peak the reason that absorb.The epicyte of all nitrogenous bases in DNA and formation bacterium, spore and virus
Albumen also show that 200nm and/or close to 280nm peak absorb.This occurs equally at core-albumen, two sweet peptides, triglycine
With (McLaren etc., Photochemistry of Proteins and Nucleic Acids, Pergamon in BA
Press,Macmillan Company,1964).Amino acid has the peak absorption bands close to 260nm.At 222nm and/or
The UV lamp launched at 282nm is absorbed producing by the maximum photon of nitrogenous base and protein.The UV-C lamp launched at 260nm
Absorbed producing by the maximum photon of the amino acid in DNA.Therefore, this 3 wavelength are the main absorptions allowing to destroy microorganism
Wave band.
Test:
3 kinds of different microorganisms are used to carry out testing to test this principle multiple comparison.By every kind of bacterization at skin
It in family name's culture dish, and is exposed to the various combination of UV photon.Accompanying drawing shows the identical culture dish with shallow and deep background, to obtain
Obtain the good contrast of result.
Fig. 3 uses serratia marcesens (Serratia marcescens) as test biology.It is exposed on the left of culture dish
The combination of 222nm and 254nm photon.It is only exposed to the photon of 282nm on the right side of culture dish.Multi-wavelength side creates and significantly changes
Kind.
Fig. 4 uses aspergillus niger (Aspergillus niger) as test biology.It is only exposed to 282nm on the left of culture dish
Photon.It is exposed to the combination of 282nm and 254nm photon on the right side of culture dish.Multi-wavelength side creates significantly improvement.
Fig. 5 uses Escherichia coli (Escherichia coli) as test biology.Be exposed on the left of culture dish 222nm and
The combination of 254nm photon.It is exposed to the combination of 282nm and 254nm photon on the right side of culture dish.Use appropriate multi-wavelength light subgroup
The right side closed creates significantly improvement.
Fig. 4 uses planktonic algae as test structure.It is not exposed to FUV photon on the left of culture dish, but right side is exposed to FUV
Photon.There occurs significant primary cellular defect.
Analyze:
All tests all use single line photons source to complete, launching close to DNA nitrogenous base of described single line photons source
The peak of single absorption bands of two absorption bandses and DNA amino acid absorbs.This provides photon and variant chromophore molecule
The interaction of group and photon are measured with the true of the interaction of other chromophoric groups in DNA molecular.
The result of first group 3 tests shows, compared with Single wavelength photon, is using the multi-wavelength narrow linear light period of the day from 11 p.m. to 1 a.m, survival
Biology substantially reduces.These tests also confirm that, the appropriate combination of double-single line photons is significant and depends on each biology.Fig. 6
Demonstrate the importance that wavelength selects.FUV photon creates significant primary cellular defect, and GUV photon is almost without effect.
The similar test carrying out cause of disease can produce the maximally effective photon wavelength combination effectively killing or inactivateing each cause of disease
List.
Content of the invention
Double-single line lamp is developed in it is critical only that of this method, and the nitrogenous base with microorganism launched by described double-single line lamp
The narrow wavelength of at least two of the absorption maximum wave band close match of DNA chromophore, protein, amino acid and other component associative keys
Ultraviolet photon wave band.Preferred embodiment is to launch the narrow line source of multi-wavelength of at least two different wave length.This spectral emissions shows
Write ground more more efficient than the standard 254nm photon for destroying DNA.The killing action time is reduced to 0.1 from tens of to hundreds of seconds
The time of second.Double-single line lamp can its by when kill the aerial cause of disease of flight.This pair-single line lamp also breaks effectively
The bad allergen based on biomembrane and albumen.
Wherein the photon energy of double-single line lamp that a line is positioned in FUV is sufficiently high, to destroy in similar action time
The carbon key of chemotoxic substances.Determine that destruction target organism or chemicals institute for obtaining short effect (killing) time uniqueness
The specific wavelength needing.Double-single line source is selected mainly to absorb chromophoric to provide with at least two of target organism or chemicals
Peak absorbs the narrow emission band of at least two of close UV light.
Relative intensity compared with another line for one line also can affect to be killed or inactivates efficiency.If three central siphon (triax
Tube) in, the ring of each room has identical width, and if outer side ring identical with the gas density of both medial chambers, then come
Will be greater than the light being sent by medial chamber from the intensity of the light of outer side ring.The gas more than 6 kinds can be produced in single three axle lamp designs
Volume density and the combination of ring position.Regulation to gas density and position provides all main disease that expectation is killed or inactivated
Former maximally efficient photon launches combination.
This equipment is advantageously used for carrying out disinfection air, all types of surface and food during normal daily routines
The method of the cost-effective improvement with sterilizing.Additionally, this equipment can be efficiently and effectively to floor, handrail, often connect
The object touching mobile population carries out disinfection.The routine disinfection in these regions can significantly reduce disease and may cause humans and animals
Injury or the propagation of sick noxious material.
Double-single line lamp radiation may be applicable to any object or the surface being sterilized and/or sterilizing.For example, can be used for
The handcart being placed on outside ward.The all appts, paper and the pen that use in ward all can pass through handcart, and leave at it
It is exposed to double-single line lamp radiation during ward.This step can prevent cause of disease to the propagation of next bit patient.Test also can measure appropriate
Exposure limit, and prevent for application on human skin and the wound area of sterilizing, hand, animal surface such as skin, fur and hair,
And the critical plastics that uses in Medical Devices and during material it may happen that any illeffects.
Because double-single line lamp source is light source, therefore can distribute light intensity by using optical fiber, thus guide it to irradiate and dredge
The different material of close level.For example, by will double-single line lamp source towards floor, simultaneously by bottom part light directing carpet or logical
The optical fiber crossing embedded brush guides to bottom scrubbing brush, and uses described double-sterilization floor, single line lamp source.Also may be used in a similar manner
Sterilization has the product in the cavity being not directly exposed to external source or region.For example, for double-single line lamp is inducted into dental cavity,
Single optical fiber with sterilization inwall and interior tissue before adding filler.
By all objects are directly exposed required open-assembly time, double-single line lamp source can be used for direct disinfection room
Microorganism in inner surface, unit and clothing, and room air.Some sources can be combined to ensure exposure to own
Total open-assembly time is simultaneously reduced in surface.This can keep survival to be the room air of isolation by preventing cause of disease after leaving indoor
Effective process is provided.One or more double-single line lamp can be moved by using robot in a plurality of directions during processing
Source simultaneously makes it process, around indoor moving, the room being polluted by bio-terrorism agent (bioterrorist agent).
Infect and the main source of terrorist (terrorist) activity points to food and material process.For many years, photon
Transmitter has been used for effectively cleaning food and surface.But, the present invention uses double-single line lamp source, due to its action time almost
It is instantaneous, be therefore cost-effective in processing food and body surface.
Double-single line lamp source is for carrying out, to food, the ameliorative way that dry type is sterilized without chemicals.Can use it for broadcasting
Disinfection seed and sprout before kind, for transporting from field to machining center, warehouse and storage, supermarket processes and kitchen is prepared simultaneously
Prepared by the food material being delivered to consumer.The cutting of meat and bird make-up room and worksheet additionally, also can use it for sterilizing
Face, so it is used for transporting the cutting machine with manufactured meat, agricultural product and other food and equipment.
The equipment of the present invention can irradiate conveyor device in the movement processing from storage to food preparation
(conveyor assemblies), the food fixed in car (stationary carts) and process approach.Also can use it for
Medical treatment on sterilization/disinfection assembly line or key component before packing.
Increasing evidence show disinfection of indoor air for reduce by patient produce in cough or when sneezing little
It is important for the infection of the microorganism that aerosol carries.At present, indoor UV sterilization is confined to use the mercuri being placed on wall
Bactericidal lamp, it has guard shield to guarantee to be irradiated to people.These lamps generally do not comprise fan, but rely on indoor air flow so that micro-
Biology passes through light.Second principle is to use to have one or more GUV mercury lamp in the effluent stream of fan or air blast
Box.This box is placed on the appropriate location in space wishing capture microorganism, and make microorganism pass through described lamp and near.
According to the report in document, in both cases, only 50% illuminated in all of microorganism in space.
Double-single line the lamp being arranged in dissimilar equipment can every time by when be exposed to up to all microorganisms
90%.A new holding equipment based on the fact that:By utilize normal airflow with by near roof compared with near floor
Air Temperature Difference and the indoor circulation air-flow causing and the condition that produces can more effectively move the air of large volume.This equipment utilization
4 or 5 blade fans operating under the low speed or the dedicated fan being exploited for auxiliary air lifting most effectively, will
Air guides extremely can be by air section in the upper chamber of double-single line or many single lines light irradiation.Lamp can be placed on fan with
Irradiate the air column of lifting in all directions.Baffle plate can prevent light from penetrating into reserved area.In described air section
In the relatively long resonance time of any microorganism, can kill or destroy major part microorganism.Passing through every time can destroyed area
In all microorganisms more than 90%.After passing through 3 times in 1 hour, 99.9% can be destroyed, it is thus achieved that having of 3 log reduction
Effect is removed.
Brief description
Fig. 1 is to show the schematic diagram that in DNA molecular, dimer is formed.
Fig. 2 is the microphoto of the atrophy bacillus under 300x and 1000x magnifying power.
Fig. 3 is the serratia marcesens biological as test.
Fig. 4 is the aspergillus niger biological as test.
Fig. 5 is the Escherichia coli biological as test.
Fig. 6 is the planktonic algae biological as test.
Fig. 7 is the perspective view of the preferred embodiment of the invention, which defines the position of the wherein significant components of double-single line lamp
Put.
Fig. 8 is the perspective view of the preferred embodiment of the invention, which defines for such as chair, handrail, work top, dish
The position of the significant components of the sterilization on the surfaces such as son, desktop and floor surface or sterilizing.
Fig. 9 is the perspective view of the preferred embodiment of the invention, which defines for kitchen process before sterilised foodstuff or
The position of the significant components of sterilization gratin before serving.
Figure 10 is the perspective view of the preferred embodiment of the invention, and it limits for the sterilization of the air-flow in air channel or sterilizing
The position of significant components.
Figure 11 is the perspective view of the preferred embodiment of the invention, and it limits and is used for the material by Portable handcart and thing
The position of the significant components of the sterilization of surface or sterilizing.
Figure 12 is the perspective view of the preferred embodiment of the invention, which defines for using large volume Low speed ceiling fan to make air
The position of significant components when being moved through room, room air being carried out disinfection or sterilizing.
Detailed description of the invention
The multi-form of the brief description present invention and preparation double-single line lamp needed for equipment.Lamp is by having two rings
Three central siphons constitute, its comprise different admixture of gas with when lamp is electrically excited produce different wave length photon.In selection
Between pipe diameter to optimize the relative intensity launched from two rooms.To the electrode being placed on internal tube and being placed in outside pipe
When applying high voltage between electrode, there is exciting of two kinds of gases.Use grid outside to allow light through lamp as external electrode
Launch.
Fig. 7 a illustrates to be formed the cross section of a part of double-single line lamp of sterilizing equipment decontaminating apparatus of the present invention.High-field electrode E1 position
In the inner tube of bicyclic lamp.Earth electrode E2 is positioned on the outside of bicyclic lamp.A kind of gas producing UV photon is positioned at inner tube 3 He
In annular region A1 between middle pipe 4.The second gas producing UV photon is positioned at annular region A2 between middle pipe 4 and outer tube 5
In.Select gas type so that the UV photon launched is absorbed by target microorganism or chemicals.UV radiates radially to 6 emission.
Change the voltage between two electrodes or electric current changes the amount that the UV of generation radiates.Change in size or each ring of each ring
Gas density change relative intensity compared with another room for the room.Preferred embodiment is to select in each room
Gas composition is to produce wavelength at the FUV of 222nm and UV-C wavelength near 254nm and 282nm or its for the wavelength.Can be by three kinds
The combination of different wave length manufactures three kinds of differences pair-single line lamp combination.
Fig. 7 b illustrates for guiding UV photon to the double-single line lamp of ad-hoc location, direction, surface, material or material.
This pair-single line lamp is shown in accompanying drawing central authorities with end-view form.The end-view of special reflector 10 is incorporated with special " the gull wing
Shape " designs, so that>90% launch the downwardly directed plane of light.Special reflector 10 be also incorporated with as reflecting material
Barium sulfate (the Ba of material2SO4) so that the photon numbers reflexing in plane maximizes.In some cases, it is desirable to covering 11 with
Protection NUV source and reflector avoid being contaminated.This covering is just transparent to UV.Special reflector also can have different
Shape is to change the directed radiation for different application.
Fig. 8 a illustrates to use the preferred embodiment of the double-single line lamp being included in hand-held rod.This rod fills for sterilization
When relaying cause of disease to the object being often touched of the pollutant of another people from a people.This embodiment can comprise sensing open
Closing 22, it closes double-single line lamp when double-single line lamp is not directed correctly to expect processed surface.This rod can provide for
Wound is processed and for processing the instrument of chronic wounds before and after operation.Additionally provide for sterilizing hospital and health is protected
The instrument of the equipment surface of reason room, operating table, handrail and support patient care.
Additionally, in the case of critical shortage gloves, dustcoat and face shield, in due course, can be by double-single line with similar side
Formula retrieves new article for these article of periodically sterilizing to substitute the place of automatically supplying.
Fig. 8 b illustrates to be positioned at double-single line lamp of the front compartment of vacuum cleaner or floor cleaning machine.Vacuum cleaning
Device can be vertical floor type or pot.It can also is that can support and carry double-single line lamp close to any equipment on floor.Weight
The part wanted is the double-single line lamp with reflector 10 being made up of the assembly described in Fig. 7 a and Fig. 7 b.As it can be seen, it is described
Assembly includes box, wheel and handle.
Fig. 9 a illustrates double-single line lamp, and it is positioned at not processed before being carried along into kitchen processing and does not prepares food
It on conveyer, and is positioned on the industrial packaging assembly line carrying the product needing sterilization.Conveyor device 24 is designed as making cruelly
It is exposed to the largest surface area of double-single line lamp.In some cases, it is desirable to several lamps 14, this is because at a double-single line
The lighting hours of lamp can not change the surface that is exposed of food or product to expose whole surface.In food and the conveying of object edge
Generally use when machine moves rotary drum or vibrator with change they towards.Fig. 9 b illustrate to be positioned at for by food from kitchen
It is delivered to before client the double-single line lamp 14 on heating lamp 15 or other heating surface sides keeping the food warm on information desk.
In another embodiment, use the food that double-single line light irradiation is cool or cold, therefore, do not use heating lamp 15.
In use, double-single line lamp can be made any size and length.In air channel 20, preferred embodiment Figure 10 a
Can have the double-single line lamp 14 supported by the sidepiece of pipeline 20, top or bottom, so that its axle and parallel current.For uniqueness
Application, the second embodiment Figure 10 b can have by the double-single line lamp source 14 supported in pipeline 20 and cylindrical reflector, so that
Its axle is vertical with air-flow.The example of this embodiment can be in the double-single line lamp at cylindrical drum center.In switching process
Middle irradiation all objects a period of time, the time span of irradiation can ensure sterilization.
Figure 11 illustrates the double-single line lamp for the equipment 26 sterilized between patient's checking tool, record, pen and patient.
Be brought into indoor for checking that the everything of patient all should be by the irradiated region in Medical handcart 24 after withdrawing from a room.
Only after doctor or health care management people use new gloves and other associated garments instead, just regained.
Figure 12 illustrates to be arranged on the preferred of the double-single line lamp on the low rate fan 28 of high speed for room air of sterilizing
Embodiment.
Although there have been described herein the preferred embodiments of the invention, but described above being merely illustrative.Related neck
Field technique personnel can carry out further modification to invention disclosed herein, and all such modifications are regarded as by appended power
Within the scope of the invention that profit claim limits.
Claims (15)
1. chlorination equipment, it comprises:
Double-single line lamp, it comprises:
Limit three central siphons of two rings therebetween;
It is chosen for producing the first admixture of gas that the first narrow wavelength photons is launched;With
Be chosen for producing be different from that the second narrow wavelength photons that the described first narrow wavelength photons launches launches be different from institute
State the second admixture of gas of the first admixture of gas;
It is positioned at the high-field electrode within inner tube;
It is positioned at the earth electrode outside outermost tubes;With
Fix with spaced relationship with described double-single line lamp and be placed so that photon to be guided into the photon reflector in region or surface,
Thus when applying energy to high-field electrode, make the generation of described sterilizing equipment decontaminating apparatus point to the photon with selected areas or surface simultaneously effectively
Ground destroys or the DNA of inactivation microorganism has switch and albumen.
2. chlorination equipment, it comprises:
First lamp and the second lamp, it comprises respectively:
Limit the coaxial pipe of two rings therebetween;
It is chosen in each lamp, produce the first and second gas mixing that the narrow wavelength photons of different first and second is launched
Thing, the admixture of gas in wherein said first lamp and wavelength are different from admixture of gas and wavelength in described second lamp;
It is positioned at the high-field electrode within the inner tube of described first lamp and the described second each lamp of lamp;
It is positioned at the earth electrode outside the outermost tubes of described first lamp and the described second each lamp of lamp;With
Fix with spaced relationship with described first lamp and the second lamp respectively and be placed to guide the photon from two lamps into region
Or the first photon reflector on surface and the second photon reflector, thus when applying energy to high-field electrode, make described sterilization
The DNA of the photon on equipment generation sensing selected areas or surface effectively destruction or inactivation microorganism has switch and albumen.
3. the sterilizing equipment decontaminating apparatus as described in claim 1 or claim 2, wherein said first and second narrow wavelength photons launch choosing
In the group of free 222nm, 254nm and 282nm composition.
4. the sterilizing equipment decontaminating apparatus as described in claim 1 or claim 2, at least one of which lamp is excited quasi-molecular lampbulb.
5. the sterilizing equipment decontaminating apparatus as described in claim 1 or claim 2, wherein said photon reflector be chosen near
The light of launching of few 90% guides to the wing guider of gull of plane.
6. the sterilizing equipment decontaminating apparatus as described in claim 1 or claim 2, wherein said photon reflector comprises for strengthening it anti-
Penetrate the barium sulfate composition of character.
7. sterilizing equipment decontaminating apparatus as claimed in claim 1, it also comprises box, wheel and handle, is suitable for use as floor cleaning.
8. sterilizing equipment decontaminating apparatus as claimed in claim 1, it also comprises:
The handle being connected with described double-single line lamp;With
For closing the surface detection apparatus of described double-single line lamp when described double-single line lamp is not near surface to be sterilized.
9. the sterilizing equipment decontaminating apparatus as described in claim 1 or claim 2, it also comprises:
To be arranged on the air channel around described lamp with the relation that described lamp is spaced, to provide the effect of being chosen in described air channel
Time, thus disinfecting air.
10. the method for disinfecting substance, it comprises the following steps:
Producing the photon of at least two wavelength, the wavelength of described photon is in the group being made up of 222nm, 254nm and 282nm;
With
Described photon is guided to material to be sterilized, thus described photon destroys or the DNA of inactivation microorganism has switch and egg
In vain.
11. methods as claimed in claim 10, wherein guide described light by described photon is reflexed to desired surface
Son.
12. methods as claimed in claim 11, are wherein reflected by the wing reflector of gull.
13. methods as claimed in claim 11, wherein said reflector is coated with barium sulfate.
14. methods being used for the material in sterilised air current, it comprises the following steps:
Directing flow into the photon source of at least two wavelength, described wavelength is selected from the group being made up of 222nm, 254nm and 282nm
In;With
Make described air-flow be exposed to described photon source, thus described photon destroys or the DNA of inactivation microorganism has switch and albumen.
15. methods as claimed in claim 14, it is further comprising the steps of:
Measure the action time (activity time) needed for the described air-flow of sterilization;With
Place described source to complete sterilization in single.
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108903346A (en) * | 2018-05-31 | 2018-11-30 | 湖南匡楚科技有限公司 | A kind of domestic intelligent shoe chest |
CN111770789A (en) * | 2017-12-29 | 2020-10-13 | 塞鲁斯公司 | System and method for treating biological fluids |
US11883544B2 (en) | 2019-06-28 | 2024-01-30 | Cerus Corporation | System and methods for implementing a biological fluid treatment device |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5843374A (en) * | 1996-10-11 | 1998-12-01 | Tetra Laval Holdings & Finance, Sa | Method and apparatus for sterilizing packaging |
CN2636131Y (en) * | 2003-05-23 | 2004-08-25 | 贺佳国 | Photoelectric air purifier for cabin of vehicle and ship |
WO2005061396A1 (en) * | 2003-11-20 | 2005-07-07 | Marine Environmental Partners, Inc. | Wastewater treatment system |
US20060188835A1 (en) * | 2005-02-22 | 2006-08-24 | Rich Nagel | Multi-wavelength dental light curing gun |
CN1898161A (en) * | 2003-12-23 | 2007-01-17 | Otv股份有限公司 | Supply device for ultraviolet lamps used in the treatment of water |
CN201052279Y (en) * | 2006-07-01 | 2008-04-30 | 谭汉卿 | Hand-hold grape disease germicidal lamp |
CN101238363A (en) * | 2005-01-31 | 2008-08-06 | S·E·内斯特尔 | Method and apparatus for sterilizing and disinfecting air and surfaces and protecting a zone from external microbial contamination |
-
2009
- 2009-01-29 CN CN201610205954.5A patent/CN106421864A/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5843374A (en) * | 1996-10-11 | 1998-12-01 | Tetra Laval Holdings & Finance, Sa | Method and apparatus for sterilizing packaging |
CN2636131Y (en) * | 2003-05-23 | 2004-08-25 | 贺佳国 | Photoelectric air purifier for cabin of vehicle and ship |
WO2005061396A1 (en) * | 2003-11-20 | 2005-07-07 | Marine Environmental Partners, Inc. | Wastewater treatment system |
CN1898161A (en) * | 2003-12-23 | 2007-01-17 | Otv股份有限公司 | Supply device for ultraviolet lamps used in the treatment of water |
CN101238363A (en) * | 2005-01-31 | 2008-08-06 | S·E·内斯特尔 | Method and apparatus for sterilizing and disinfecting air and surfaces and protecting a zone from external microbial contamination |
US20060188835A1 (en) * | 2005-02-22 | 2006-08-24 | Rich Nagel | Multi-wavelength dental light curing gun |
CN201052279Y (en) * | 2006-07-01 | 2008-04-30 | 谭汉卿 | Hand-hold grape disease germicidal lamp |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111770789A (en) * | 2017-12-29 | 2020-10-13 | 塞鲁斯公司 | System and method for treating biological fluids |
US11554185B2 (en) | 2017-12-29 | 2023-01-17 | Cerus Corporation | Systems and methods for treating biological fluids |
CN108903346A (en) * | 2018-05-31 | 2018-11-30 | 湖南匡楚科技有限公司 | A kind of domestic intelligent shoe chest |
US11883544B2 (en) | 2019-06-28 | 2024-01-30 | Cerus Corporation | System and methods for implementing a biological fluid treatment device |
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