AU4634199A - Surface coatings - Google Patents
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- AU4634199A AU4634199A AU46341/99A AU4634199A AU4634199A AU 4634199 A AU4634199 A AU 4634199A AU 46341/99 A AU46341/99 A AU 46341/99A AU 4634199 A AU4634199 A AU 4634199A AU 4634199 A AU4634199 A AU 4634199A
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- Australia
- Prior art keywords
- substrate
- optionally substituted
- alkyl
- group
- plasma
- Prior art date
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/62—Plasma-deposition of organic layers
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/22—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of inorganic material, other than metallic material
- C23C16/30—Deposition of compounds, mixtures or solid solutions, e.g. borides, carbides, nitrides
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/44—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
- C23C16/50—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges
- C23C16/515—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating using electric discharges using pulsed discharges
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M10/00—Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
- D06M10/02—Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements ultrasonic or sonic; Corona discharge
- D06M10/025—Corona discharge or low temperature plasma
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M10/00—Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
- D06M10/04—Physical treatment combined with treatment with chemical compounds or elements
- D06M10/08—Organic compounds
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M10/00—Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
- D06M10/04—Physical treatment combined with treatment with chemical compounds or elements
- D06M10/08—Organic compounds
- D06M10/10—Macromolecular compounds
Description
WO 00/05000 PCT/GB99/02121 1 Surface Coatings The present invention relates to the coating of surfaces, in particular to the production of oil- and water- repellent 5 surfaces, as well as to coated articles obtained thereby. Oil- and water- repellent treatments for a wide variety of surfaces are in widespread use. For example, it may be desirable to impart such properties to solid surfaces, such 10 as metal, glass, ceramics, paper, polymers etc. in order to improve preservation properties, or to prevent or inhibit soiling. A particular substrate which requires such coatings are 15 fabrics, in particular for outdoor clothing applications, sportswear, leisurewear and in military applications. Their treatments generally require the incorporation of a fluoropolymer into or more particularly, fixed onto the surface of the clothing fabric. The degree of oil and water 20 repellency is a function of the number and length of fluorocarbon groups or moieties that can be fitted into the available space. The greater the concentration of such moieties, the greater the repellency of the finish. 25 In addition however, the polymeric compounds must be able to form durable bonds with the substrate. Oil- and water repellent textile treatments are generally based on fluoropolymers that are applied to fabric in the form of an aqueous emulsion. The fabric remains breathable and 30 permeable to air since the treatment simply coats the fibres with a very thin, liquid-repellent film. In order to make these finishes durable, they are sometimes co-applied with cross-linking resins that bind the fluoropolymer to fibres. Whilst good levels of durability towards laundering and dry- WO 00/05000 PCT/GB99/02121 2 cleaning can be achieved in this way, the cross-linking resins can seriously damage cellulosic fibres and reduce the mechanical strength of the material. Chemical methods for producing oil- and water-repellent textiles are disclosed 5 for example in WO 97/13024 and British patent No 1,102,903 or M. Lewin et al., 'Handbood of Fibre Science and Technology' Marcel and Dekker Inc., New York, (1984) Vol 2, Part B Chapter 2. 10 Plasma deposition techniques have been quite widely used for the deposition of polymeric coatings onto a range of surfaces. This technique is recognised as being a clean, dry technique that generates little waste compared to conventional wet chemical methods. Using this method, 15 plasmas are generated from small organic molecules, which are subjected to an ionising electrical field under low pressure conditions. When this is done in the presence of a substrate, the ions, radicals and excited molecules of the compound in the plasma polymerise in the gas phase and react 20 with a growing polymer film on the substrate. Conventional polymer synthesis tends to produce structures containing repeat units which bear a strong resemblance to the monomer species, whereas a polymer network generated using a plasma can be extremely complex. 25 The success or otherwise of plasma polymerisation depends upon a number of factors, including the nature of the organic compound. Reactive oxygen containing compounds such as maleic anhydride, has previously been subjected to plasma 30 polymerisation (Chem. Mater. Vol. 8, 1, 1996). US Patent No 5,328,576 describes the treatment of fabric or paper surfaces to impart liquid repellent properties by WO 00/05000 PCT/GB99/02121 3 subjecting the surfaces to a pre-treatment with an oxygen plasma, followed by plasma polymerisation of methane. However, plasma polymerisation of the desirable oil and 5 water repellent fluorocarbons have proved more difficult to achieve. It has been reported that cyclic fluorocarbons undergo plasma polymerisation more readily than their acyclic counterparts (H. Yasuda et al., J. Polym. Sci., Polym. Chem. Ed. 1977, 15, 2411). The plasma polymerization 10 of trifluoromethyl-substituted perfluorocyclohexane monomers has been reported (A. M. Hynes et al., Macromolecules, 1996, 29, 18-21). A process in which textiles are subjected to plasma 15 discharge in the presence of an inert gas and subsequently exposed to an F-containing acrylic monomer is described in SU-1158-634. A similar process for the deposition of a fluroalkyl acrylate resists on a solid substrate is described in European Patent Application No. 0049884. 20 Japanese application no. 02011606 describes the plasma polymerisation of compounds including fluorosubstituted acrylates. In that process, a mixture of the fluorosubstituted acrylate compounds and an inert gas are 25 subjected to a glow discharge. Copending International Patent application based upon British Patent Application Nos. 9712338.4 and 9720078.6 describes a -method method for producing polymer and 30 particular halopolymer coatings which are water and/or oil repellent on surfaces by the plasma deposition of monomer compounds which include carbon-carbon double bonds. The applicants have found that the method can be extended to the deposition of other compounds. In particular monomers which WO 00/05000 PCT/GB99/02121 4 are unsaturated in that they contain no carbon-carbon double bonds may be employed in the process and similar advantageous results achieved. 5 According to the present invention there is provided a method of coating a surface with a polymer layer, which method comprises exposing said surface to a pulsed plasma comprising a monomeric saturated organic compound, said compound comprising an optionally substituted alkyl chain of 10 at least 5 carbon atoms optionally interposed with a heteroatom; so as to form an oil or water repellent coating on said substrate. The term "saturated" as used herein means that the monomer 15 does not contain multiple bonds (i.e. double or triple bonds) between two carbon atoms which are not part of an aromatic ring. The term "heteroatom" includes oxygen, sulphur, silicon or nitrogen atoms. Where the alkyl chain is interposed by a nitrogen atom, it will be substituted so 20 as to form a secondary or tertiary amine. Similarly, silicons will be substituted appropriately, for example with two alkoxy groups. Other terms used herein include "halo" or "halogen" which 25 refer to fluorine, chlorine, bromine and iodine. Particularly preferred halo groups are fluoro. The term "aryl" refers to aromatic cyclic groups such as phenyl or napthyl, in particular phenyl. The term "alkyl" refers to straight or branched chains of carbon atoms, suitably of up 30 to 50 carbon atoms in length. Derivatives of alkyl groups, such as would be understood by "alkoxy" include such groups. The term "heterocyclyl" includes aromatic and non aromatic rings or ring systems, suitably containing up to 12 atoms, up to three of which may be heteroatoms.
WO 00/05000 PCT/GB99/02121 5 The monomeric compound used in the process of the invention may comprise one or more optionally substituted alkyl chains, either as part of a branched alkane or as part of a 5 more complex structure including rings and other functional groups. These may be present either in the monomer used as a starting material, or may be created in the monomer on application of the plasma, for example by the ring opening of an optionally substituted cycloalkyl monomer. 10 Suitable optional substituents for the monomeric compounds of the invention include halo, cyano, nitro, oxo, epoxide, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted 15 heterocyclyl, C (0),,Rl, OR', S (O) mR, NR 2
R
3 , C (0) NR 2
R
3 , OC (O) NR 2 R', =NOR 2 , -NR 2 C (0) IR2, -NR'CONR 2 R2, -C=NOR', -N=CR 2 R', S(O)mNR 2
R
3 or -- NR2S (0) mR where R', R2 and R' are independently selected from hydrogen or alkyl, aralkyl, cycloalkyl, aryl or heterocyclyl, any of which may be optionally substituted, 20 or R2 and R 3 together form an optionally substituted ring which optionally contains further heteroatoms such as sulphur, oxygen and nitrogen, n is an integer of 1 or 2, m is 0 or an integer of 1-3. 25 Suitable optional substituents for aryl, aralkyl and cycloalkyl and heterocyclyl groups R, R 2 and R3 include halo, perhaloalkyl, mercapto, hydroxy, alkoxy, oxo, heteroaryloxy, alkenyloxy, alkynyloxy, alkoxyalkoxy, aryloxy (where the aryl group may be substituted by halo, nitro, or 30 hydroxy), cyano, nitro, amino, mono- or di-alkyl amino, alkylamido or oximino. Suitable alkyl chains, which may be straight or branched, have from 5 to 50 carbon atoms, more suitably from 6 to 20 WO 00/05000 PCT/GB99/02121 6 carbon atoms, and preferably from 8 to 15 carbon atoms, provided at least 5 carbon atoms form a straight chain. 5 Monomeric compounds where the chains comprise unsubstituted alkyl groups are suitable for producing coatings which are water repellent. By substituting at least some of the hydrogen atoms in these chains with at least some halogen atoms, oil repellency may also be conferred by the coating. 10 Thus in a preferred aspect, the monomeric compounds include haloalkyl moieties or comprise haloalkyls. Therefore, preferably the plasma used in the method of the invention will comprise a monomeric saturated haloalkyl containing 15 organic compound. Particularly suitable monomeric organic compounds are those of formula (I) 20 R4 R5 I I R'--- C C- R" R3 R 25 where R 4 , R5, R' R 7 and R are independently selected from hydrogen, halogen, alkyl, haloalkyl or aryl optionally substituted by halo; and R' is a group X-R where R is an 30 alkyl or haloalkyl group and X is a bond; a group of formula -C(0)O(CH 2 )xY- where x is an integer of from 1 to 10 and Y is a bond or a sulphonamide group; or a group (O),R 11
(O),(CH
2 )I- where R" is aryl optionally substituted by halo, p is 0 or 1, s is 0 or 1 and t is 0 or an integer of 35 from 1 to 10, provided that where s is 1, t is other than 0.
WO 00/05000 PCT/GB99/02121 7 Suitable haloalkyl groups for R 4 , R', R 6 , R', and R3 are fluoroalkyl groups. The alkyl chains may be straight or branched and may include cyclic moieties and have, for example from 1 to 6 carbon atoms. 5 For R", the alkyl chains suitably comprise 1 or more carbon atoms, suitably from 1-20 carbon atoms and preferably from 6 to 12 carbon atoms. 10 Preferably R1 is a haloalkyl, and more preferably a perhaloalkyl group, particularly a perfluoroalkyl group of formula CF 2
+
1 1 where z is an integer of 1 or more, suitably from 1-20, and preferably from 6-12 such as 8 or 10. 15 Where X is a group -C(O)O(CH 2 )yY-, y is an integer which provides a suitable spacer group. In particular, y is from 1 to 5, preferably about 2. Suitable sulphonamide groups for Y include those of formula 20 -N(R")SO2 where R" is hydrogen, alkyl or haloalkyl such as
C
1 4 alkyl, in particular methyl or ethyl. The monomeric compounds used in the method of the invention preferably comprises an C- 2 ,alkane optionally substituted by 25 halogen, in particular a perhaloalkane, and especially a perfluoroalkane. Compounds of formula (I) are either known compounds or they can be prepared from known compounds using conventional 30 methods. Suitable plasmas for use in the method of the invention include non-equilibrium plasmas such as those generated by alternating current (AC) (e.g. radiofrequencies (Rf), WO 00/05000 PCT/GB99/02121 8 microwaves) or direct current (DC). They may operate at atmospheric or sub-atmospheric pressures as are known in the art. 5 The plasma may comprise the monomeric compound alone, in the absence of other gases or in mixture with for example an inert gas. Plasmas consisting of monomeric compound alone may be achieved as illustrated hereinafter, by first evacuating the reactor vessel as far as possible, and then 10 purging the reactor vessel with the organic compound for a period sufficient to ensure that the vessel is substantially free of other gases. The surface coated in accordance with the invention may be 15 of any solid substrate, such as fabric, metal, glass, ceramics, paper or polymers. In particular, the surface comprises a fabric substrate such as a cellulosic fabric, to which oil- and/or water-repellency is to be applied. Alternatively, the fabric may be a synthetic fabric such as 20 an acrylic/nylon fabric. The fabric may be untreated or it may have been subjected to earlier treatments. For example, it has been found that treatment in accordance with the invention can enhance the 25 water repellency and confer a good oil-repellent finish onto fabric which already has a silicone finish which is water repellent only. Precise conditions under which the plasma polymerization 30 takes place in an effective manner will vary depending upon factors such as the nature of the polymer, the substrate etc. and will be determined using routine methods and/or the techniques illustrated hereinafter. In general however, polymerisation is suitably effected using vapours of WO 00/05000 PCT/GB99/02121 9 compounds of formula (I) at pressures of from 0.01 to 10 mbar, suitably at about 0.2mbar. A glow discharge is then ignited by applying a high 5 frequency voltage, for example at 13.56MHz. The applied fields are suitably of average power of up to 50W. Suitable pulsed fields are those which are applied in a sequence which yields very low average powers, for example 10 of less than 1OW and preferably of less than 1W. Examples of such sequences are those in which the power is on for 20ps and off for from 10000ps to 20000is. The fields are suitably applied for a period sufficient to 15 give the desired coating. In general, this will be from 30 seconds to 3 hours, preferably from 2 to 30 minutes, depending upon the nature of the monomer compound used and the substrate etc. 20 Plasma polymerisation in accordance with the invention particularly at low average powers has been found to result in the deposition of highly fluorinated coatings which exhibit super-hydrophobicity. 25 In a preferred embodiment, the pulses are applied at a variable rate, with relatively long pulses applied, for example of from 1 to 10 secs on initially, reducing down to short pulses for example of from 100pls to 1p1s on and 10p1s to 1000pts off, later in the process. It is believed that such 30 a regime leads to improved coatings because the initial long pulse leads to greater fragmentation of the monomer, leading to a more disorganised and therefore strongly bonding layer directly adjacent the substrate. Shorter late pulses means that the upper layers deposited retain a more organised WO 00/05000 PCT/GB99/02121 10 structure and so contain a greater number of long chains, which are responsible for the oil and water repellency on the surface. 5 Suitably the compound of formula (I) includes a perfluoroalkylated tail or moiety, in which case, the coating obtained by the process of the invention may have oleophobic as well as hydrophobic surface properties. 10 Thus the invention further provides a hydrophobic or oleophobic substrate which comprises a substrate comprising a coating of a alkyl polymer and particularly a haloalkyl polymer which has been applied by the method described above. In particular, the substrates are fabrics but they 15 may be solid materials such as biomedical devices. In a further aspect the invention provides the use of an optionally substituted alkane or optionally substituted cycloalkane having at least 5 carbon atoms and particularly 20 a perhaloalkane in the production of water and/or oil repellent coatings by pulsed plasma deposition methods. The invention will now be particularly described by way of example with reference to the accompanying diagrammatic 25 drawings in which: Figure 1 shows a diagram of the apparatus used to effect plasma deposition; and 30 Figure 2 is a graph showing the characteristics of pulsed wave plasma polymerisation of perfluorododecane.
WO 00/05000 PCT/GB99/02121 Example 1 Plasma Polymerisation of perfluorododecane Rerfluorododecane (C,,F,,) was placed into a monomer tube (I) (Fig. 1). A series of plasma polymerisation experiments 5 were carried out in an inductively coupled cylindrical plasma reactor vessel (2) of 5cm diameter, 470cm 3 volume, base pressure of 7xlO- 3 mbar, and with a leak rate of better than 2x10- 3 cm 3 min'. The reactor vessel (2) was connected by way of a "viton" 0-ring (3), a gas inlet (4) and a needle 10 valve (5) to the monomer tube (1). A thermocouple pressure gauge (6) was connected by way of a Young's tap (7) to the reactor vessel (2). A further Young's tap (8) connected with an air supply and a third (9) 15 lead to an E2M2 two stage Edwards rotary pump (not shown) by way of a liquid nitrogen cold trap (10). All connections were grease free. An L-C matching unit (11) and a power meter (12) was used to 20 couple the output of a 13.56 Mhz R.F. generator (13), which was connected to a power supply (14), to copper coils (15) surrounding the reactor vessel (2). This arrangement ensured that the standing wave ratio (SWR) of the transmitted power to partially ionised gas in the reactor 25 * peseYA42uleeadsbgnmingmisedtor (16) was used to trigger the R.F power supply, and a cathode ray oscilloscope (17) was used to monitor the pulse width and amplitude. The average power 30 <P> delivered to the system during pulsing is given by the following formula: <P> = Pe,(Ton/ (Ton + Toff) ) WO 00/05000 PCT/GB99/02121 12 where T.,/ (T., + Tff) is defined as the duty cycle and P, is the average continuous wave power. In order to carry out polymerization/deposition reactions 5 the reactor vessel (2) was cleaned by soaking overnight in a chloros bleach bath, then scrubbing with detergent and finally rinsing with isopropyl alcohol followed by oven drying. The reactor vessel (2) was then incorporated into the assembly as shown in Figure 1 and further cleaned with a 10 50W air plasma for 30 minutes. Next the reactor (2) vessel was vented to air and the substrate to be coated (19), in this case a glass slide, was placed in the centre of the chamber defined by the reactor vessel (2) on a glass plate (18). The chamber was then evacuated back down to base 15 pressure (7.0 x 10-3mbar). Perfluoroalkane vapour was then introduced into the reaction chamber at a constant pressure of -0.2mbar and allowed to purge the plasma reactor, followed by ignition of the glow 20 discharge. Typically 2-15 minutes deposition time was found to be sufficient to give complete coverage of the substrate. After this, the R.F generator was switched off and the perfluoroalkane vapour allowed to continue to pass over the substrate for a further 5 minutes before evacuating the 25 reactor back down to base pressure, and finally venting up to atmospheric pressure. The experiments were carried out with average powers in the range of from 0.3 to 50W. The XPS spectrum of the product 30 of a pulsed wave plasma polymer deposition onto a glass slide was taken.
WO 00/05000 PCT/GB99/02121 13 Figure 2 shows the C (1s) XPS spectrum for a 5 minute pulsed plasma polymerisation experiment where:- Pc, = 70W
T
0 n = 20pAs 5 T 0 ff = 20000s <P> = 0.07W The chemical composition of the deposited coating for pulsed plasma deposition is given in Table 2 below. 10 Table 2 Experimental Theoretical F:C ratio 1.86 2.17
%CF
2 group 47.9 83.3 %CF, group 18.5 16.7
Claims (21)
1. A method of coating a surface with a polymer layer, 5 which method comprises exposing said surface to a pulsed plasma comprising a monomeric saturated organic compound, said compound comprising an optionally substituted alkyl chain of at least 5 carbon atoms optionally interposed with a heteroatom; so as to form an oil or water repellent 10 coating on said substrate.
2. A method according to claim 1 wherein the alkyl chains are substituted by halogen. 15
3. A method according to claim 2 wherein the alkyl chains are perhalogenated.
4. A method according to claim 1 wherein the monomeric organic compound is a compound bf formula (I) 20 R 4 R 5 R'- C C- R 7 1 1 25 R R9 where R 4 , R 5 , R"' R 7 and R' are independently selected from hydrogen, halogen, alkyl, haloalkyl or aryl optionally 30 substituted by halo; and R 9 is a group X-R where R1 0 is an alkyl or haloalkyl group and X is a bond; a group of formula -C(0)O(CH 2 )xY- where x is an integer of from 1 to 10 and Y is a bond or a sulphonamide group; or a group (0)pR"(0)s(CH 2 )t- where R" is aryl optionally substituted by WO 00/05000 PCT/GB99/02121 15 halo, p is 0 or 1, s is 0 or 1 and t is 0 or an integer of from 1 to 10, provided that where s is 1, t is other than 0.
5. A method according to claim 4 wherein the compound of 5 formula (I) comprises a C 6 2 5 alkane optionally substituted by halogen.
6. A method according to claim 5 wherein the C,-, alkane is a Ce 25 perfluoroalkane. 10
7. A method according to any one of the preceding claims wherein the substrate is a fabric, metal, glass, ceramics, paper or polymer material. 15
8. A method according to claim 7 wherein the substrate is a cellulosic fabric.
9. A method according to claim 7 wherein the substrate is a synthetic fabric. 20
10. A method according to any one of the preceding claims wherein the monomeric organic compound is in the form of a vapour at a pressure of from 0.01 to 10 mbar. 25
11. A method according to any one of the preceding claims wherein the plasma is created by applying an alternating frequency voltage.
12. A method according to any one of the preceding claims 30 wherein the average power of the electrical field applied is up to 50W. WO 00/05000 PCT/GB99/02121 16
13. A method according to any one of the preceding claims wherein the pulsed fields are applied in a sequence which yields an average power of less than 10W. 5
14. A method according to claim 13 wherein the average power is less than 1W.
15. A method according to claim 13 or claim 14 wherein the pulses are applied in a sequence in the power is on for 10 20pis and off for from 10000sis to 20000ps.
16. A method according to any one of the preceding claims wherein the pulses are applied at a variable rate. 15
17. A method according to claim 16 wherein the length of the pulses decreases during the treatment.
18. A hydrophobic or oleophobic substrate which comprises a substrate comprising a coating of an alkyl polymer 20 obtained by a method according to any one of the preceding claims.
19. The use of an optionally substituted alkane or optionally substituted cycloalkane having at least 5 carbon 25 atoms in the production of water and/or oil repellent coatings by pulsed plasma deposition methods.
20. The use of claim 19 wherein the alkane or cycloalkane is perhalogenated. 30
21. A method for producing an water and/or oil repellent coating on a substrate, substantially as hereinbefore described with reference to the Example.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9816077 | 1998-07-24 | ||
GBGB9816077.3A GB9816077D0 (en) | 1998-07-24 | 1998-07-24 | Surface coatings |
PCT/GB1999/002121 WO2000005000A1 (en) | 1998-07-24 | 1999-07-02 | Surface coatings |
Publications (2)
Publication Number | Publication Date |
---|---|
AU4634199A true AU4634199A (en) | 2000-02-14 |
AU749438B2 AU749438B2 (en) | 2002-06-27 |
Family
ID=10836057
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU46341/99A Expired AU749438B2 (en) | 1998-07-24 | 1999-07-02 | Surface coatings |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP1104341A1 (en) |
JP (2) | JP4436567B2 (en) |
CN (1) | CN1320062A (en) |
AU (1) | AU749438B2 (en) |
CA (1) | CA2338538C (en) |
GB (2) | GB9816077D0 (en) |
NZ (1) | NZ509522A (en) |
WO (1) | WO2000005000A1 (en) |
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CN100340595C (en) * | 2003-01-30 | 2007-10-03 | 欧洲等离子公司 | Method for providing a coating on the surface of product with an open cell structure throughout its structure and use of such a method |
JP2007505219A (en) * | 2003-09-09 | 2007-03-08 | ダウ グローバル テクノロジーズ インコーポレイティド | Chemical vapor deposition with glow discharge |
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JP2010534727A (en) * | 2007-07-17 | 2010-11-11 | ピーツーアイ リミティド | Method for making an article liquid-proof by plasma graft polymerization |
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1998
- 1998-07-24 GB GBGB9816077.3A patent/GB9816077D0/en not_active Ceased
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1999
- 1999-07-02 NZ NZ509522A patent/NZ509522A/en not_active IP Right Cessation
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- 1999-07-02 EP EP99929552A patent/EP1104341A1/en not_active Withdrawn
- 1999-07-02 GB GB0101150A patent/GB2354249B/en not_active Expired - Lifetime
- 1999-07-02 CA CA002338538A patent/CA2338538C/en not_active Expired - Lifetime
- 1999-07-02 WO PCT/GB1999/002121 patent/WO2000005000A1/en not_active Application Discontinuation
- 1999-07-02 AU AU46341/99A patent/AU749438B2/en not_active Expired
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2009
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GB0101150D0 (en) | 2001-02-28 |
CA2338538A1 (en) | 2000-02-03 |
JP2002521179A (en) | 2002-07-16 |
EP1104341A1 (en) | 2001-06-06 |
GB9816077D0 (en) | 1998-09-23 |
NZ509522A (en) | 2002-11-26 |
AU749438B2 (en) | 2002-06-27 |
JP4436567B2 (en) | 2010-03-24 |
GB2354249A (en) | 2001-03-21 |
GB2354249B (en) | 2002-06-05 |
JP2010042410A (en) | 2010-02-25 |
CA2338538C (en) | 2009-12-15 |
CN1320062A (en) | 2001-10-31 |
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