WO2001073356A1 - Biostatic filter - Google Patents
Biostatic filter Download PDFInfo
- Publication number
- WO2001073356A1 WO2001073356A1 PCT/AU2001/000339 AU0100339W WO0173356A1 WO 2001073356 A1 WO2001073356 A1 WO 2001073356A1 AU 0100339 W AU0100339 W AU 0100339W WO 0173356 A1 WO0173356 A1 WO 0173356A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- filter
- composition according
- air
- agent
- filtrate
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/02—Loose filtering material, e.g. loose fibres
- B01D39/04—Organic material, e.g. cellulose, cotton
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/0027—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours with additional separating or treating functions
- B01D46/0028—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours with additional separating or treating functions provided with antibacterial or antifungal means
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2279/00—Filters adapted for separating dispersed particles from gases or vapours specially modified for specific uses
- B01D2279/50—Filters adapted for separating dispersed particles from gases or vapours specially modified for specific uses for air conditioning
Definitions
- This invention relates to air-conditioning systems and more particularly to a method of, and composition for, reduction in pathogens associated with the filters in such systems.
- the invention has been developed primarily for use in air-conditioning
- Air conditioning systems such as are commonly provided in office, residential, health care and other buildings incorporate air filters.
- An example of such a filter employs non-woven polyester fibres as media to filter airborne particulates in excess of about 10 microns in size from the air, but filters are made from a wide variety of materials, in many different constructions and grades.
- the function of the filter is to trap dust and particulate contaminants. This trapped matter (the "filtrate”) provides a haven for the growth of pathogens such as fungi, bacteria, viruses, allergens, yeasts, and moulds.
- Conditions for the growth of such organisms are especially favourable during periods of high humidity such as may occur when the system is off, for example at night, but also arise during normal operation.
- the presence of organisms is highly undesirable because they can cause illness or death in humans and animals, create odours and can damage or destroy a wide variety of materials.
- endo toxins and mycotoxins which are breakdown components of fungal and bacterial cell walls and which are known human respiratory allergens. In some individuals they can trigger asthma attacks, and in all cases have been shown to cause immune response. Over a period of exposure this reduces the ability of the immune system to respond to antagonists and leaves the subject more prone to infection by bacteria, viruses, etc. Also of concern are fungal spores, bacterial spores and bacteria.
- air filters are prepared from or include natural materials such as cellulose and in that case are rapidly degraded under moist conditions by certain fungi.
- the invention provides an air filter including a composition, said composition including a biostatic or biocidal agent wherein the agent is adapted to migrate through particulates accumulating in use on the filter.
- the biostatic or biocidal agent is selected to have bacteriostatic and/or fungistatic properties.
- the particulates usually accumulate in layers and the biostatic or biocidal agent of the invention migrates through the layer to the outside surface (air/particulate interface) where organic matter would otherwise multiply.
- the biocide is not bound to the filter surface but is adapted to migrate through the accumulating dust and particulate matter on the filter. Particles in the layer become coated with biocide or biostat.
- the treatment is bacteriostatic or fungistatic. That is to say, it is sufficient that the treating agent stops colonisation on the filter rather than kills organisms in a colonised filter.
- biocidal compositions may be used.
- the invention provides a composition for application to an air filter including:
- biocidal or biostatic agent is adapted to migrate through a filtrate accumulating, in use, on a surface of the air filter
- composition further includes a surfactant and desirably a fluorosurfactant.
- the composition includes one or more rheological additives for example a thickening agent, a gelling agent, or a viscosity modifier.
- the invention provides a method of treating a filtrate on a filter including the step of adding to the filter or to the filtrate a biocidal or biostatic agent adapted to migrate through the filtrate
- the invention provides a method of reducing airborne contaminants in air including the step of: treating a filter with an agent according to the second aspect, passing air through the filter whereby to accumulate contaminants as a filtrate on the filter , and allowing the biocide to migrate into the filtrate.
- Fig 1 is a photomicrograph (x 100) of a new untreated air conditioning dust filter prior to use
- Fig 2 is a photomicrograph ( lOO) showing an untreated filter similar to that of Fig 1 after 11 months in use in a building air conditioning system
- Fig 3 is a photomicrograph (xlOO) showing a treated filter similar to that of Fig 1 after 11 months in use in a building air conditioning system
- Fig 4 is a graph comparing the number of colony fonning units ("cfu's") per gram of a filter treated in accordance with the invention with an untreated filter as a function of time in use over 11 months BEST MODES OF PERFORMING THE INVENTION
- the present inventor has discovered that the application of biocides to filter fibres as in the past is relatively ineffective because; while tins treatment can prevent fungal and biocidal activity directly on the filter fibres themselves, as dust accumulate on the filter, the outer surface of the dust becomes removed from the biocide bound to the filter fibres and pathogens then grow on the outside of this dusty residue (that is to say separated from the biocide treated fibres). Thus, as the filter clogs, the biocidal activity reduces. This explains why good results can be obtained in tests applying an innoculum to the prior art filters in the laboratory but without good results being obtained in actual installed continuous use.
- the present invention provides a biocide which remains effective over much longer periods, if not over the useful life of the filter by providing a biocidal preparation adapted to migrate through the layer or layers of accumulating filtrate on the filter towards the surface (air/p articulate interface) where the micro-organisms tend to colonise, Surprisingly this can be achieved despite the higher velocity of air at the surface of such residue.
- compositions according to the invention are effective because the humectant draws in water which acts as a vehicle for the solution and transport of biostat or biocide (or of a combination of biostats and/or of biocides).
- the surface tension of the vehicle is effectively lowered by the one or more surface active agents.
- the biocidal composition is permitted to migrate to the outermost surface by the aqueous vehicle, maintaining its efficacy against pathogenic organisms, which otherwise would grow on the surface of the particulate layer and in gaps in the particulate residue.
- the biocide wets the exterior surface of individual particles as well as the exterior surface of the particulate layer.
- Example 1 In a preferred embodiment of the invention, an air filter is coated with a solution containing the dispersion or solution of biocide and humectant in a solvent.
- an air conditioning filter according to Australian grade "F5" was treated .
- the filter was made from a needled non- oven polyester fibre fabric and had a total surface area of about 3.5 square metres.
- the filter thickness was 10-12 mm and its density was about 280-300 grams per square metre (gsm). A typical fibre diameter would be in the range of 6-15 denier.
- the filter was treated by spraying with a solution having a formulation as shown in example 2.
- Example 2 A basic formulation of a treating solution is as follows: Calcium chloride (humectant) 5-25% Kathon 886MW (biostat) 0.04%
- Kathon 886MW is a preservative obtainable from Rohm & Haas Corp.
- Fluorad FC 129 is a fluorosurfactant available from 3M corp. Example 3
- a preferred formulation for the treating solution is as follows: Calcium chloride (humectant) 14 -18%
- rheological additives e.g. viscosity modifiers, gelling agents, thixotropic agents or the like
- the type and quantity of rheological additive can be selected having regards to conditions of use.
- the preferred treatment is very strongly hydroscopic, taking in moisture from the air passing through the filter and becoming a liquid. This liquids penetration into an accumulating filtrate layer is further enhanced by the incorporation in the treatment of a surface active agent which ensures penetration against the air flow by virtue of low surface tension.
- the biocides in the formulation are water soluble or partly water soluble and therefore migrate into and through the filtrate layer as part of the treatment.
- Other active ingredients may be incorporated into the formulation for permeation through the filtrate, for example fire retardants, airflow promoters or viscosity reducing agents, deodorisers and so forth.
- Example 4 A filter according to example 1 was treated by spraying with a solution according to example 3 to a level of 230 ml of treating solution per square meter. The treated filter was then dried using dry air. It will be understood that the filter could be coated by dipping or any other convenient method and dried using heat, a vacuum or by any other suitable means or combination of means. The dried filter was then placed into a sealed container, such as a sealed plastic bag, until ready for use.
- the filter When the filter was to be used, it was removed from its sealed container, and placed in its operational position in an air-conditioning system.
- the humectant in a filter prepared in accordance with the invention will begin to absorb water from the environment. This absorption continues through to a stage where a saturated solution of the biocide forms in which the concentration depends on the relative humidity of the air. During the liquefaction process, the biocidal components are partially or completely dissolved in the humectant solution along with the surfactants.
- the resulting liquid treatment solution has an extremely low surface tension and high osmolality making it an ideal penetrant.
- This treatment progressively penetrates and encapsulates the contaminant particles.
- the encapsulating penetrating treatment which contains an efficacious level of biocide not only kills micro-organisms carried on the airbome contaminant, but also ensures that no microbiological activity takes place in the layer of filtrate itself.
- the growth of bacteria and pathogens is naturally higher than in diy air.
- the present invention provides greater biocidal activity when it is most needed, i.e. during times of high humidity. Reduced biocidal activity may be a consequence of drier air, however it is anticipated that the number and growth of pathogens during such dry conditions would not be so high. These conditions result in an extension of the biocidal life-time of the filter.
- the present invention is not directed towards the prevention of clogging of the filter by preventing growth of the biomass, but rather is directed to controlling colonisation by organisms on the filter and in the accumulating residue and ultimately to produce air which is reduced in pathogens.
- Example 5
- Filters treated according to example 4 were placed in service.
- the treated filters were found to be effective in service for periods of six months or more. At the end of six months, the filter was removed, cleaned, and retreated with fresh composition according to example 1.
- Spore forming materials put a load on the human immune system of those breathing the air. Dead cells, if they become airborne, cause asthma in those susceptible.
- a further advantage of the present invention is that the humectant maintains a level of moisture at the filtrate surface which reduces spore and cell refluidization.
- Figures 1-3 are photomicrographs at x 100 magnification showing the effect of treatment after 11 months in use (fig 3) compared to untreated filter material before use (fig 1) and after 11 months use (fig 2).
- a comparison of the used untreated sample of fig 2 with the unused sample of fig 1 shows that use results in significant growth of fungal filaments (which appear as fine threads) about the larger diameter filter fibres. Entrapped dirt and dust particles are also visible after use.
- the treated filter of fig 3 shows no significant growth of micro-organisms after 11 months exposure although entrapped dirt and dust particles are' naturally clearly visible.
- Example.6 A series of identical new filters were taken and 20% of them were treated as in . example 4 with the composition of example 3. The remaining 80% of the series were left untreated. The treated and untreated filters were put into the same air handling system, such that the treated filters were alternated with untreated filters. On a monthly basis samples were taken from both a treated and an adjacent untreated filter and the number of viable fungal and bacterial species were counted. The results (expressed as colony forming units ("cfu's”)/gram of filter are shown in fig 4 as a function of time in months. The rate of colonisation of the treated filter was not significantly different from that of the untreated filter during the first month.
- cfu's colony forming units
- Suitable biocides for use in the invention include, but are not limited to, 2-bromo- 2-nitropropane-l,3-diol (Bronopol); Isothiazolines such as methyl, or chloromethyl isothiazolinone (Kathon 886 MW); Methyl or propyl or butyl parahydroxybenzoates; sorbic acid, benzoic acid and salts of these acids, phenoxy ethanol; triclosan; diclosan; dichlorophen; chlorhexidine gluconate, orthophenylphenol; benzalkonium halides; and other quaternary biocides orthobenzylparachlorophenol, substituted diphenyl ethers.
- Bronopol 2-bromo- 2-nitropropane-l,3-diol
- Isothiazolines such as methyl, or chloromethyl isothiazolinone (Kathon 886 MW)
- a preferred humectant for use in the invention is calcium chloride.
- examples of other humectants are glycerol, sorbitol, ethylene glycol, PEG, propylene glycol, 1,3 butylene glycol, PCA (2-Pyrrolidone-5-carboxylic acid), sodium sulphate, sodium hydroxide, lactic acid and derivatives, sodium chloride and the like.
- humectants also act as surfactants.
- One example is sodium dioctylsulphosuccinate.
- a preferred surfactant class for use in the invention is fluoro surfactants, such as Fluorad FC129. These are preferred because they have a profound ability to reduce surface tension. However other surfactants can be employed.
- the surfactant may be non-ionic (e.g.
- anionic surfactants such as sodium dodecylbenzenesulphonate, sodium dioctylsulphosuccinate, sodium salts of sulphonated or sulphated organic ethoxylates or propoxylates
- catio ic surfactants such as Cetrimonium Chloride or such as secondary, tertiary and quaternary organoamines
- amphoteric surfactants such Cocamidopropylene Betaine
- rheological agents which may be included are sodium carboxymethylcellulose; hydroxyethylcellulose; hydroxypropylcellulose; polyethylene glycols; polypropylene glycols; polyvinyl alcohol; polyvinyl acetate, polyvinylpyrrolidone and copolymers of these, hydroxypropyl guar, xanthan gum, chitosan, acrylated copolymers, polyacrylic polymers (carbopols) and the like.
- water soluble polymers would be similarly advantageous.
- composition in the examples was applied to the filter from an aqueous solution or suspension, it may be possible and advantageous to apply the humectant and biostat to the filter as a solid or from a non aqueous solvent and such compositions are within the scope of the invention.
- compositions according to the invention can be applied to filters of any material. Tests have been conducted with filters of polypropylene, viscose, rayon, cellulosics, and glass fibre. However the principle of operation herein described is adaptable to filters of other materials and of other construction (such as for example woven, non-woven, spunbond, meltblown, laminates and the like).
- the treating agent may employ one or more biocides and may be formulated based on the principles herein taught in a variety of formulations.
- a filter may be treated in situ by admitting a composition according to the invention as a spray downstream of the filter or by direct application (continuously or intermittently) of a biostat onto the filtrate layer of a filter in service, or prior to removal.
- the treatment may also be reapplied to a filter removed from service, with or without removal of filtrate.
Abstract
Description
Claims
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2404816A CA2404816C (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
US10/239,714 US6802891B2 (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
AU4210801A AU4210801A (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
IL15197501A IL151975A (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
NZ521751A NZ521751A (en) | 2000-03-29 | 2001-03-27 | Filter adapted for long lasting biocidal or biostatic activity by applying a water soluable biocidal or biostatic agent and a humectant |
JP2001571036A JP4846164B2 (en) | 2000-03-29 | 2001-03-27 | Air filter |
KR1020027012964A KR100903715B1 (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
MXPA02009500A MXPA02009500A (en) | 2000-03-29 | 2001-03-27 | Biostatic filter. |
EP01914836A EP1269088B1 (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
AU2001242108A AU2001242108B9 (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
DE60120943T DE60120943T2 (en) | 2000-03-29 | 2001-03-27 | BIOSTATIC FILTER |
HK03104215A HK1052214A1 (en) | 2000-03-29 | 2003-06-12 | Biostatic filter |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AUPQ6563 | 2000-03-29 | ||
AUPQ6563A AUPQ656300A0 (en) | 2000-03-29 | 2000-03-29 | Biostatic filter |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001073356A1 true WO2001073356A1 (en) | 2001-10-04 |
Family
ID=3820659
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/AU2001/000339 WO2001073356A1 (en) | 2000-03-29 | 2001-03-27 | Biostatic filter |
Country Status (20)
Country | Link |
---|---|
US (1) | US6802891B2 (en) |
EP (1) | EP1269088B1 (en) |
JP (2) | JP4846164B2 (en) |
KR (1) | KR100903715B1 (en) |
CN (1) | CN1186569C (en) |
AR (1) | AR027729A1 (en) |
AT (1) | ATE331190T1 (en) |
AU (1) | AUPQ656300A0 (en) |
CA (1) | CA2404816C (en) |
DE (1) | DE60120943T2 (en) |
DK (1) | DK1269088T3 (en) |
ES (1) | ES2269362T3 (en) |
IL (1) | IL151975A (en) |
MX (1) | MXPA02009500A (en) |
MY (1) | MY124876A (en) |
NZ (1) | NZ521751A (en) |
PT (1) | PT1269088E (en) |
TW (1) | TW531443B (en) |
WO (1) | WO2001073356A1 (en) |
ZA (1) | ZA200207791B (en) |
Cited By (4)
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WO2004103071A1 (en) * | 2003-05-21 | 2004-12-02 | Novapharm Research (Australia) Pty Ltd | Biofilm growth prevention |
WO2006058370A1 (en) * | 2004-11-30 | 2006-06-08 | Alpha Technologies Corporation Ltd | Improved sterilising filter arrangement, apparatus & method |
AU2004241665B2 (en) * | 2003-05-21 | 2009-10-08 | Novapharm Research (Australia) Pty Ltd | Biofilm growth prevention |
GR1010135B (en) * | 2021-02-03 | 2021-12-06 | Ηλεκτρονικα Μετρητικα Συστηματα Α.Ε., | Three-action air-purifying device |
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AUPQ656300A0 (en) * | 2000-03-29 | 2000-04-20 | Novapharm Research (Australia) Pty Ltd | Biostatic filter |
AUPQ656200A0 (en) * | 2000-03-29 | 2000-04-20 | Novapharm Research (Australia) Pty Ltd | Chemical upgrading of filters |
US20030075047A1 (en) * | 2001-10-22 | 2003-04-24 | Normand Bolduc | Bactericidal after-filter device |
US7080828B2 (en) * | 2001-12-22 | 2006-07-25 | Phoenix Ag | Clarification basin membrane |
US20060021302A1 (en) * | 2004-07-30 | 2006-02-02 | Bernard Bobby L | Anti-microbial air filter |
US20070012186A1 (en) * | 2005-03-11 | 2007-01-18 | Wilson Todd S | System and method of dehumidifying and filtering air |
WO2006113967A1 (en) * | 2005-04-27 | 2006-11-02 | Novapharm Research (Australia) Pty Ltd | Biostatic filter and water insoluble biocide formulation therefor |
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JP5801528B2 (en) | 2005-12-14 | 2015-10-28 | スリーエム イノベイティブ プロパティズ カンパニー | Antibacterial adhesive film |
US20070253909A1 (en) * | 2006-05-01 | 2007-11-01 | Medi-Flex, Inc. | Aqueous Antiseptic Solution and Compatible Cationic Dye for Staining Skin |
US20070254854A1 (en) * | 2006-05-01 | 2007-11-01 | Medi-Flex, Inc. | Aqueous Antiseptic Solution and Compatible Anionic Dye for Staining Skin |
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US20090191250A1 (en) * | 2008-01-28 | 2009-07-30 | Water Visions International, Inc. | Antimicrobial Composite Material and Method for Fluid Treatment |
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WO2011088185A2 (en) | 2010-01-18 | 2011-07-21 | 3M Innovative Properties Company | Air filter with sorbent particles |
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CN105013252B (en) * | 2014-04-16 | 2016-08-24 | 黄山城市绿洲空气过滤器科技有限公司 | A kind of coating and the application in air filtration thereof |
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US10926219B2 (en) | 2015-08-28 | 2021-02-23 | Serionix, Inc. | Gas filters for basic contaminants |
US10639588B2 (en) | 2015-08-28 | 2020-05-05 | Serionix, Inc. | Gas filters for acidic contaminants |
US10299473B2 (en) | 2017-04-28 | 2019-05-28 | American Sterilizer Company | Low pH phenolic disinfectant without para tertiary amylphenol |
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-
2000
- 2000-03-29 AU AUPQ6563A patent/AUPQ656300A0/en not_active Abandoned
-
2001
- 2001-03-27 JP JP2001571036A patent/JP4846164B2/en not_active Expired - Lifetime
- 2001-03-27 WO PCT/AU2001/000339 patent/WO2001073356A1/en active IP Right Grant
- 2001-03-27 US US10/239,714 patent/US6802891B2/en not_active Expired - Lifetime
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004103071A1 (en) * | 2003-05-21 | 2004-12-02 | Novapharm Research (Australia) Pty Ltd | Biofilm growth prevention |
AU2004241665B2 (en) * | 2003-05-21 | 2009-10-08 | Novapharm Research (Australia) Pty Ltd | Biofilm growth prevention |
US8524799B2 (en) | 2003-05-21 | 2013-09-03 | Novapharm Research (Australia) Pty Ltd | Biofilm growth prevention |
WO2006058370A1 (en) * | 2004-11-30 | 2006-06-08 | Alpha Technologies Corporation Ltd | Improved sterilising filter arrangement, apparatus & method |
GR1010135B (en) * | 2021-02-03 | 2021-12-06 | Ηλεκτρονικα Μετρητικα Συστηματα Α.Ε., | Three-action air-purifying device |
Also Published As
Publication number | Publication date |
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JP2011218355A (en) | 2011-11-04 |
AUPQ656300A0 (en) | 2000-04-20 |
DE60120943T2 (en) | 2007-02-15 |
DE60120943D1 (en) | 2006-08-03 |
ES2269362T3 (en) | 2007-04-01 |
CA2404816C (en) | 2011-07-12 |
AR027729A1 (en) | 2003-04-09 |
US6802891B2 (en) | 2004-10-12 |
JP4846164B2 (en) | 2011-12-28 |
CA2404816A1 (en) | 2001-10-04 |
JP2003529041A (en) | 2003-09-30 |
IL151975A0 (en) | 2003-04-10 |
IL151975A (en) | 2005-07-25 |
CN1427937A (en) | 2003-07-02 |
TW531443B (en) | 2003-05-11 |
ATE331190T1 (en) | 2006-07-15 |
EP1269088A4 (en) | 2003-05-28 |
KR20030007487A (en) | 2003-01-23 |
US20030116022A1 (en) | 2003-06-26 |
PT1269088E (en) | 2006-11-30 |
ZA200207791B (en) | 2003-05-09 |
CN1186569C (en) | 2005-01-26 |
EP1269088B1 (en) | 2006-06-21 |
KR100903715B1 (en) | 2009-06-19 |
NZ521751A (en) | 2004-06-25 |
EP1269088A1 (en) | 2003-01-02 |
JP5613623B2 (en) | 2014-10-29 |
MY124876A (en) | 2006-07-31 |
MXPA02009500A (en) | 2004-07-30 |
DK1269088T3 (en) | 2006-10-30 |
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