WO2011093785A1 - Method for applying nanoparticles - Google Patents
Method for applying nanoparticles Download PDFInfo
- Publication number
- WO2011093785A1 WO2011093785A1 PCT/SE2011/050092 SE2011050092W WO2011093785A1 WO 2011093785 A1 WO2011093785 A1 WO 2011093785A1 SE 2011050092 W SE2011050092 W SE 2011050092W WO 2011093785 A1 WO2011093785 A1 WO 2011093785A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- nanoparticles
- photocatalytic
- sheet
- panel
- μηη
- Prior art date
Links
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/18—Paper- or board-based structures for surface covering
- D21H27/22—Structures being applied on the surface by special manufacturing processes, e.g. in presses
- D21H27/26—Structures being applied on the surface by special manufacturing processes, e.g. in presses characterised by the overlay sheet or the top layers of the structures
- D21H27/28—Structures being applied on the surface by special manufacturing processes, e.g. in presses characterised by the overlay sheet or the top layers of the structures treated to obtain specific resistance properties, e.g. against wear or weather
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F13/00—Coverings or linings, e.g. for walls or ceilings
- E04F13/07—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor
- E04F13/08—Coverings or linings, e.g. for walls or ceilings composed of covering or lining elements; Sub-structures therefor; Fastening means therefor composed of a plurality of similar covering or lining elements
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F15/00—Flooring
- E04F15/02—Flooring or floor layers composed of a number of similar elements
Definitions
- the disclosure generally relates to methods of applying nanopartides on a surface to create a layer with embedded photo catalyst nanopartides.
- the invention relates to a method to achieve a homogenous distribution of nanopartides in the upper layer of boards and panels.
- WFF Wood Fibre Floor
- US2009/0208646A1 describes a wet-in-wet application of a coating to an impregnated overlay by means of a coating inlet.
- the control of the thickness of the layer is obtained by wipers that wipe of the excess coating.
- the document shows a method of producing an overlay, in particular for laminates, involving impregnation of a paper with the following method steps:
- US37981 1 1 describes the incorporation of particles in the paper machine where the particles can be found throughout the paper, entangled by the fibres.
- WO2007144718 discloses a hard nanoparticle suspension applied to the resin pre-treated carrier sheet.
- the method states that the suspension comprises resin.
- the method comprises adding the suspension by means of a wire doctor roll and/or a raster roll or other methods comprising rolls and/or knifes. Also air- knives.
- Embodiments of the invention relates to a method of applying nanoparticles on a surface to create a sheet or a surface layer with photocatalytic nanoparticles.
- the aim is to improve the effect of the photocatalytic nanoparticles when the particles are embedded in the sheet or the surface layer, i.e. keeping the activity level at a high level and maintaining the desired properties of the sheet or the layer with the embedded particles.
- a first aspect of the invention is a method of manufacturing a sheet comprising photocatalytic nanoparticles, the method comprising the steps of: • impregnating a sheet with a polymer resin, preferably comprising wear resistant particles;
- the sheet may comprise cellulose fibres.
- the impregnation fluid composition comprises a solvent comprising water.
- the method may comprise a step between impregnating and spraying step in which step the polymer resin is partly dried.
- the impregnation fluid composition may comprise photocatalytic nanoparticles and a solvent, said solvent being selected from water, ethylene glycol, butyl ether, aliphatic linear, branched or cyclic or mixed aromatic-aliphatic alcohols, such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol, benzyl alcohol or methoxypropanol or combinations thereof.
- a second aspect of the invention is a method to produce a laminate board or panel by arranging the sheet produced according to the first aspect on a core, preferably an HDF panel and applying heat and pressure.
- a third aspect of the invention is a method of manufacturing a sheet comprising photocatalytic nanoparticles, the method comprising the steps of: ⁇ mixing the photocatalytic nanoparticles in a polymer resin, to obtain an impregnation mix;
- a fourth aspect of the invention is a method to produce a paper sheet comprising photocatalytic nanoparticles in the paper plant, preferably prior to rolling of the paper.
- a fifth aspect of the invention is a method to produce a WFF panel comprising photocatalytic nanoparticles, the method comprises the step of:
- Step 2 and 3 of the method may be applied in any of the methods disclosed in WO2009/065769 and WO2009/124704 for production of WFF panels.
- the method is preferably performed in the numbered order 1 -4.
- the organic solvent preferably comprises ketone, such as acetone and methyl ethyl ketone, and/or alcohol, such as ethanol, propanol and methanol, and/or acetate, such as butyl acetate, ethyl acetate.
- the organic solvent is in a preferred embodiment ethanol.
- the method comprised the step of applying, preferably before step 2, a fluid with a wetting agent on the mix, preferably in the form of water containing 1 % weight content of BYK-348 from BYK Chemie.
- a fluid with a wetting agent on the mix preferably in the form of water containing 1 % weight content of BYK-348 from BYK Chemie.
- the fluid with the wetting agent and the organic solvent may also be applied together.
- the embedded nanoparticles have a primary particle size or crystal size of ⁇ 50 nm, such as ⁇ 30 nm, preferably a primary particle or crystal size of ⁇ 20 nm.
- the embedded nanoparticles have a cluster or aggregate size of ⁇ 100 nm, such as ⁇ 80 nm, preferably a cluster or aggregate size of ⁇ 60 nm, such as ⁇ 40 nm, and even more preferably a cluster or aggregate size of ⁇ 30 nm, such as ⁇ 20 nm.
- said nanoparticles may be easier to disperse homogeneously in said overlaying layer, and said layer become more optically transparent.
- the concentration of said nanoparticles in said impregnation fluid may be > 1 wt%, such as > 5 wt%, preferably a concentration of said nanoparticles > 10 wt%, such as > 15 wt%, and even more preferably a concentration of said nanoparticles > 20 wt%, such as > 25 wt%.
- the nanoparticles in said impregnation fluid composition may have a cluster or aggregate size of ⁇ 100 nm, such as ⁇ 80 nm, preferably a cluster or aggregate size of ⁇ 60 nm, such as ⁇ 40 nm, and even more preferably a cluster or aggregate size of ⁇ 30 nm, such as ⁇ 20 nm.
- the amount of impregnation fluid composition per square meter of overlaying sheet(s) may be in the range 1 -200 ml/m2, such as in the range 5-100 ml/m2, and preferably in the range 10-50 ml/m2, such as 20-40 ml/m2, of said impregnation fluid composition per square meter of overlaying sheet(s) to be impregnated.
- the polymer resin used for sa id polymer resin composition comprising nanoparticles may be selected from the group comprising melamine formaldehyde resin, phenol formaldehyde resin, urea formaldehyde resin, melamine urea formaldehyde resin, acrylamide resins, urethane resins, epoxy resins, silicon resins, acrylic resins, vinylic resins or mixtures thereof.
- the photocatalytic nanoparticles in said nanoparticle polymer resin composition may be introduced as a dry powder, as a paste or as a suspension and then dispersed in the polymer resin.
- a solvent of said suspension of photocatalytic nanoparticles to be dispersed in the polymer resin composition is selected from water, ethylene glycol, butyl ether, aliphatic linear, branched or cyclic or mixed aromatic-aliphatic alcohols, such as methanol, ethanol, propanol, isopropanol, butanol, isobutanol, benzyl alcohol or methoxypropanol or combinations thereof.
- Embodiments of the invention may in a sixth aspect be obtained by a method of manufacturing a board or a panel, the method comprising
- the coating fluid may in any of the above aspects be applied to said material surface by spraying, dipping, rolling, brushing or by other conventional application methods.
- the amount of coating fluid composition per square meter of said material surface may be in the range 1 -200 ml/m2, such as in the range 5-100 ml/m2, and preferably in the range 10-50 ml/m2, such as 15-25 ml, of said coating fluid composition per square meter of said material surface.
- Fig 1 Illustrates a production line for producing an overlay paper.
- Fig 2 Illustrates a production line for producing an overlay paper
- the present invention is concerned with manufacturing of an overlay or boards or panels, such as laminate boards or panels, comprising different types of photocatalytic nanoparticles, which makes the manufactured products
- Each layer and process step can be preferred from the others e.g. depending upon the price of the laminate boards and panels (low cost/high cost product) and the facilities available by the laminate manufacturers.
- Laminate boards and panels are typically made of a base of fibre board (mainly high density fibre board HDF) and 3 or more sheets: a decor sheet, an overlay sheet of cellulose on top and one or more backing sheets sitting on the opposite side of the fibre board base to balance the board and prevent it from curving. Other sheets are often placed between the fibre board and the decor sheet.
- the decor sheet could be monochromatic or patterned to look like e.g. wood, cork, stone, tiles or a more abstract pattern.
- the overlay sheet typically contains wear resistant particles, normally a certain amount of alumina oxide (AI2O3), to give the laminate better abrasive resistance.
- the overlay sheet is impregnated with a polymer resin, typically melamine formaldehyde resin.
- the other sheets are also impregnated with resin.
- the decor sheet is typically impregnated with melamine formaldehyde resin whereas phenol formaldehyde resin often is used in the core of the laminate.
- the laminate board or panel is assembled applying heat and pressure, making the resin polymerise in a thermosetting reaction. After lamination the polymerised overlay sheet and decor paper constitute the top layer of the laminate board or panel and thus needs to be optically transparent right from the upper surface of the laminate through to the decorative print of the decor paper.
- the photocatalytic nanoparticles are applied as a wet-in-wet spray coating (43, 40) to the upper and/or lower surface of the paper (10), after a first (42) and/or a second (41 ) impregnation of the paper (10) with a resin and wear resistant particles, preferably aluminium oxide.
- the paper may be dried (44,45) after each impregnation.
- the photocatalytic nanoparticles are applied after the impregnation step but before the drying step.
- the paper (10) is in a first step (46) moistened with a resin and/or impregnated in a resin through.
- This method of spraying the photocatalytic nanoparticles may be incorporated in any production line for producing overlay or decor paper, also in the line shown in fig 1 and described above under US2009/0208646.
- the spraying of the photocatalytic nanoparticles may in the fig 1 line be performed at any stage after the
- nanoparticles is an electronically controlled Autojet Pulsajet B10000jjau.
- Preferred spray velocity of overlay or decor paper may be > 1 m/s, such as > 2 m/s, preferably a velocity of > 5 m/s, such as > 8 m/s, and even more preferably a velocity of > 10 m/s.
- the photocatalytic nanoparticles are applied as a wet-on- dry spray coating to the upper and/or lower surface of the overlay and/or decor paper, after a first or a second impregnation of the paper with resin and wear resistant particles, preferably aluminium oxide.
- the paper is normally dried after each impregnation.
- the photocatalytic nanoparticles may be mixed with a wetting agent and/or an alcohol prior to the spray coating step to improve the wettability of the impregnation fluid on the overlay and/or decor sheet.
- the photocatalytic nanoparticles may be applied as a combination between wet-in-wet and wet-in-dry spray coating.
- photocatalytic nanoparticles are applied as a polymer mixture in the resin impregnation step.
- photocatalytic nanoparticles are incorporated into an overlay sheet, e.g., in the decor paper itself prior to polymer resin impregnation.
- an overlay sheet e.g., in the decor paper itself prior to polymer resin impregnation.
- Said photocatalytic nanoparticle impregnation and drying/curing steps may be incorporated into an existing production line immediately prior to the polymer resin impregnation of said overlay sheet or decor paper or said photocatalytic impregnated and cured overlay sheet or decor paper can be stored until needed.
- a suitable type of nanoparticle for use in the coating fluid composition is Titania.
- the nanoparticles of Titania may according to some aspects of the present invention further comprise other elements. In some embodiments such elements may be introduced into said nanoparticles with the aim to improve the
- the solvent of said coating fluid composition may comprise water, methanol, ethanol or isopropanol or combinations thereof, or may just be water.
- manufactured board or panel may be increased by repeating said coating step several times.
- a preferred embodiment of the produced impregnated paper comprises discrete photocatalytic nanoparticles on and in said overlay sheet or decor paper. Said nanoparticles or clusters of nanoparticles may in many applications according to the present invention be of substantially the same size as the effective particle size in said impregnation fluid composition.
- the produced impregnated paper comprising the photocatalytic nanoparticles, may be used in all known process, to produce laminated building panel, preferably floorboards, wall panels and kitchen tabletops
- the photocatalytic composition to be dispersed in the polymer resin may preferably comprise photocatalytically active nanoparticles of Titania (TiO2).
- said nanoparticles comprise the anatase and/or the rutile and/or the brookite crystal form of Titania or a combination thereof.
- said photocatalytically active nanoparticles are according to the present invention predominantly present in their final crystal form in said composition i.e. no heat treatment is required for transformation of said nanoparticles into their active form.
- the average primary particle size or crystallite size of the nanoparticles e.g. Titania expressed as an equivalent spherical diameter may preferably be below 30 nm, such as below 20 nm, and preferably below 15 nm, such as below 10 nm.
- the average primary particle size or crystallite size may be measured by X-ray Diffraction (XRD) using Scherer's formula. It is further preferred that the particle size distribution of said nanoparticles is relatively narrow.
- the photocatalytic composition to be dispersed in the polymer resin may be added to the polymer resin at any given time.
- the photocatalytic composition is dispersed into the polymer resin immediately prior to the impregnation of overlay sheets or decor papers with polymer resin. Said dispersion process may be aided by a specially designed machine or apparatus.
- This example illustrates the production of a polymeric surface containing embedded nanoparticles.
- the particles were applied as dispersion via a spray system onto the freshly impregnated polymeric surface while still wet.
- the following dispersion was used as a feedstock. 30% TiO2 dispersion in water containing particle agglomerates of no bigger size than 80 nm as determined using the Particle Matriz Nanotrack NPA 252. The stock solution was then sprayed onto freshly impregnated melamine paper right after the paper had left the impregnation roller. The dispersion was applied onto the paper using an autojet spray system, pumping the fluid to the nozzles via a low pressure tank whit a pressure of 1 .8 bar. The nozzles were pulsejet nozzles with air atomizing tips (air pressure 1 .5 bar) placed 35 cm above the freshly impregnated paper right in front of the entrance to the first drying oven.
- the autojet system was set to deliver 30ml fluid/m2 of paper; the paper was then dried in two consecutive heating ovens. This yielded a melamine paper with embedded TiO2 agglomerates of a very small size, penetrating approximately the first couple of hundred micrometers of the melamine paper.
- Example 2 Wet on Dry
- This example illustrates the production of a polymeric surface containing embedded nanoparticles.
- the particles were applied as dispersion via a spray system onto the polymeric surface after this was dried in the heating oven.
- This example illustrates the production of a polymeric surface containing embedded nanoparticles.
- the particles were applied as dispersion via a spray system onto the raw paper before the paper was impregnated with melamine.
- Test I Applying a photocatalytic top layer by impregnation of overlay paper wet-in-wet by spraying.
- Test II Applying a photocatalytic top layer by impregnation of overlay paper wet-on-dry by spraying.
- Test III Applying a photocatalytic top layer by impregnation of overlay paper wet-on-dry by spraying on raw overlay paper before melamine impregnation.
- Test III Wet- in-dry 4 4 2
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- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Catalysts (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Claims
Priority Applications (14)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201180006669.6A CN102753357B (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
NZ600856A NZ600856A (en) | 2010-01-29 | 2011-01-28 | Method of applying photocatalytic nanoparticles on wood fibre board panels |
BR112012017934-9A BR112012017934B1 (en) | 2010-01-29 | 2011-01-28 | METHOD OF MANUFACTURING A SHEET THAT INCLUDES PHOTOCATALYTIC NANOPARTICLES, LAMINATED PLATE AND LAMINATED PANEL |
MX2012008414A MX342884B (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles. |
RU2012134551/12A RU2557519C2 (en) | 2010-01-29 | 2011-01-28 | Method of application of nanoparticles |
EP18181446.8A EP3444122B1 (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
AU2011209990A AU2011209990B2 (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
EP11737371.2A EP2528752B1 (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
KR1020127020926A KR20120123411A (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
UAA201209784A UA105945C2 (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
CA2786676A CA2786676C (en) | 2010-01-29 | 2011-01-28 | Method of applying photocatalyst nanoparticles on boards and panels |
SG2012045878A SG182270A1 (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
ZA2012/05612A ZA201205612B (en) | 2010-01-29 | 2012-07-25 | Method for applying nanoparticles |
HRP20181436TT HRP20181436T1 (en) | 2010-01-29 | 2018-09-06 | Method for applying nanoparticles |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE1050095 | 2010-01-29 | ||
SE1050095-7 | 2010-01-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011093785A1 true WO2011093785A1 (en) | 2011-08-04 |
Family
ID=44319586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/SE2011/050092 WO2011093785A1 (en) | 2010-01-29 | 2011-01-28 | Method for applying nanoparticles |
Country Status (16)
Country | Link |
---|---|
EP (2) | EP2528752B1 (en) |
KR (1) | KR20120123411A (en) |
CN (1) | CN102753357B (en) |
AU (1) | AU2011209990B2 (en) |
BR (1) | BR112012017934B1 (en) |
CA (1) | CA2786676C (en) |
ES (1) | ES2844176T3 (en) |
HR (1) | HRP20181436T1 (en) |
MX (1) | MX342884B (en) |
MY (1) | MY158396A (en) |
NZ (1) | NZ600856A (en) |
RU (1) | RU2557519C2 (en) |
SG (1) | SG182270A1 (en) |
UA (1) | UA105945C2 (en) |
WO (1) | WO2011093785A1 (en) |
ZA (1) | ZA201205612B (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102011056186A1 (en) | 2011-12-08 | 2013-06-13 | SÜDDEKOR GmbH | Process for producing a layer arrangement, layer arrangement and their use |
US20150083319A1 (en) * | 2013-09-25 | 2015-03-26 | Välinge Photocatalytic Ab | Method of applying a photocatalytic dispersion |
WO2014003944A3 (en) * | 2012-05-29 | 2015-07-02 | Niles Nanofabrix | Nanomaterial based fabric reinforced with prepreg methods, and composite articles formed therefrom |
US9375750B2 (en) | 2012-12-21 | 2016-06-28 | Valinge Photocatalytic Ab | Method for coating a building panel and a building panel |
US9573126B2 (en) | 2012-03-20 | 2017-02-21 | Valinge Photocatalytic Ab | Photocatalytic composition |
US9963609B2 (en) | 2009-03-23 | 2018-05-08 | Valinge Photocatalytic Ab | Production of titania nanoparticle colloidal suspensions with maintained crystallinity by using a bead mill with micrometer sized beads |
US11045798B2 (en) | 2011-07-05 | 2021-06-29 | Valinge Photocatalytic Ab | Coated wood products and method of producing coated wood products |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016010472A1 (en) * | 2014-07-16 | 2016-01-21 | Välinge Innovation AB | Method to produce a thermoplastic wear resistant foil |
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2011
- 2011-01-28 MY MYPI2012003246A patent/MY158396A/en unknown
- 2011-01-28 KR KR1020127020926A patent/KR20120123411A/en active IP Right Grant
- 2011-01-28 AU AU2011209990A patent/AU2011209990B2/en active Active
- 2011-01-28 ES ES18181446T patent/ES2844176T3/en active Active
- 2011-01-28 RU RU2012134551/12A patent/RU2557519C2/en active
- 2011-01-28 WO PCT/SE2011/050092 patent/WO2011093785A1/en active Application Filing
- 2011-01-28 SG SG2012045878A patent/SG182270A1/en unknown
- 2011-01-28 NZ NZ600856A patent/NZ600856A/en unknown
- 2011-01-28 MX MX2012008414A patent/MX342884B/en active IP Right Grant
- 2011-01-28 CN CN201180006669.6A patent/CN102753357B/en active Active
- 2011-01-28 BR BR112012017934-9A patent/BR112012017934B1/en active IP Right Grant
- 2011-01-28 EP EP11737371.2A patent/EP2528752B1/en active Active
- 2011-01-28 CA CA2786676A patent/CA2786676C/en active Active
- 2011-01-28 UA UAA201209784A patent/UA105945C2/en unknown
- 2011-01-28 EP EP18181446.8A patent/EP3444122B1/en active Active
-
2012
- 2012-07-25 ZA ZA2012/05612A patent/ZA201205612B/en unknown
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2018
- 2018-09-06 HR HRP20181436TT patent/HRP20181436T1/en unknown
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Cited By (12)
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UA105945C2 (en) | 2014-07-10 |
EP2528752A4 (en) | 2015-11-04 |
AU2011209990B2 (en) | 2015-04-30 |
BR112012017934A2 (en) | 2020-08-25 |
BR112012017934B1 (en) | 2021-08-17 |
MY158396A (en) | 2016-10-14 |
NZ600856A (en) | 2013-07-26 |
KR20120123411A (en) | 2012-11-08 |
RU2012134551A (en) | 2014-03-10 |
CN102753357B (en) | 2015-04-15 |
EP3444122B1 (en) | 2020-11-18 |
MX342884B (en) | 2016-10-14 |
AU2011209990A1 (en) | 2012-07-26 |
ZA201205612B (en) | 2013-09-25 |
CA2786676C (en) | 2020-01-14 |
SG182270A1 (en) | 2012-08-30 |
RU2557519C2 (en) | 2015-07-20 |
EP2528752A1 (en) | 2012-12-05 |
EP3444122A1 (en) | 2019-02-20 |
MX2012008414A (en) | 2012-12-05 |
CN102753357A (en) | 2012-10-24 |
ES2844176T3 (en) | 2021-07-21 |
HRP20181436T1 (en) | 2018-11-02 |
EP2528752B1 (en) | 2018-07-04 |
CA2786676A1 (en) | 2011-08-04 |
AU2011209990A8 (en) | 2012-10-18 |
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