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Plasma polymerisation polymers

A number of authors describe significant improvements in the polymer coating quality obtained by pulsed plasma polymerisation cf. CW). If these claims are substantiated, it would seem likely that research effort will focus increasingly on this mode of plasma deposition. The question arises as to whether the pulsed environment is simply an extrapolation of the low power CW environment, or whether it represents an entirely different plasma environment altogether. [Pg.126]

Reproducibility problems in the production of polymer layers as described above can sometimes occur. Since washing steps and drying procedures are often incorporated to remove loosely bound material, and changes in intensity or duration of these steps can result in different layers. Thus the amoimt of the immobilised protein will be different and reduce the reproducibility of the sensors response. The use of thick organic films produced by this method can also lead to frequency instabihty and loss of sensitivity. It is also difficult to control film thickness and homogeneity, which also effect the reproducibility of the surface produced. Weak adhesion between the polymer and the substrate can also be a problem. Methods, such as plasma polymerisation and electropolymerisation, have been developed to overcome these problems and to gain more control over the layer parameters. [Pg.249]

Electropolymerisation of layers again offers control over the growth and thickness of the film. Production of the layer is also quite simplistic. The gold surface is placed in a solution containing the polymer, which is electropoly-merised onto the surface at the appropriate potential for the desired time. After this a very stable highly branched structure is formed on the surface that can be further modified to immobihse the antibodies. As with plasma polymerised methods many crystals can be easily prepared at a time. [Pg.250]

Finally, an approach which is based on plasma polymerisation treatment enables the coating of CNTs with a very thin ( 3 nm) polymer layer. Polymer... [Pg.78]

Fabrication of polymers for these small and integrated sensors should be by the new processing technologies, which can produce accurate, mass reproducible and thin polymers. The polymers fabricated by conventional methods may have potential problems such as the difficulty of preparing thin (<1 pm) and homogeneous films. A plasma-polymerised film offers a new alternative [19]. The plasma-polymerised film is achieved in a glow discharge or plasma in the vapour phase. Such films are thin (< 1 pm), pinhole-free, flat-surface structures and are chemically and mechanically stable. [Pg.276]

Ultrathin polymer films can be prepared using two kinds of technology. The first includes wet processes like LB, spreading, dipping or solvent casting methods. The other is dry processing, such as physical vapour deposition (PVD) and chemical vapour deposition (CVD). Of these methods, the CVD methods, such as plasma polymerisation, are frequently used to make polymer thin films [24-26]. [Pg.276]

Plasma polymers are deposited as a thin film and/or as a powder on surfaces contacting a glow discharge of organic or organometallic feed gases. Plasma polymerisation is a specific type of plasma chemistry, which involves reactions between plasma species, between plasma on the surface [35]. [Pg.277]

However, inhomogenity in deposition rate is caused by an increase in pressure. Thus most plasma polymerisation is carried out at pressures below 1 Torr, in order to obtain the increased interaction of the plasma with a polymer surface to obtain homogeneous films [54, 55]. [Pg.282]

A structural and electrical survey for conductive phenomena was performed using acetonitrile plasma polymerised film [68]. This polymer was discovered to have two states of electrical condnction. Electrical conduction in the high condnction state was sensitive to the nature of electrode material. Electrical conduction in the low conduction state was unaffected by the electrode material. [Pg.285]

A conducting plasma polymer was processed using TCNQ with quinoline [71]. The results showed that the plasma-polymerised quinoline and TCNQ had conductivities of 10 Q cm and 10 Q cm, respectively. However, a high conductivity of 10 Q cm was measured for the plasma polymers mixed with TCNQ and quinoline. [Pg.286]

Four techniques are used in most industrial processes for the polymerisation of monomers to obtain corresponding polymers. These include (i) bulk or mass, (ii) solution, (iii) suspension and (iv) emulsion polymerisation techniques. However, other techniques such as interfadal, electrochemical and plasma polymerisation are also used to obtain different polymers, particularly in laboratory or low scale production. [Pg.14]

Physically controlled Plasma polymerisation (mask) Polymer Any 76... [Pg.519]

Journal of Inorganic Organometallic Polymers 4, No.4, Dec. 1994, p.425-30 IMPROVEMENT OF THE ADHESION OF SILICONE TO ALUMINIUM USING PLASMA POLYMERISATION Costantino G Zeik D B Clarson S J Cincinnati, University... [Pg.60]

Plasma polymerisation of appropriate monomers onto the surface of accelerator particles, in the present case cyclohexylbenzothiazole sulphenamide (CBS), allow the accelerating effect during the vulcanisation of rubber compounds to be controlled. Using squalene as a model substance for rubber, the effect of CBS modified with three different monomers on scorch time and crosslink density was studied. 21 refs. Articles from this journal can be requested for translation by subscribers to the Rapra produced International Polymer Science and Technology. [Pg.51]

Mention has already been made of the effectiveness of corona or plasma treatment in increasing the influence of subsequent or concurrent polymer treatment. As examples of polymers used in this way, mention can be made of reactive cationic polysiloxane [294] and polymerisation on the fibre of tetrafluoroethylene or hexafluoropropylene [299]. Water repellency was also improved by the fluorinated polymers. Tetrafluoroethylene gave superior shrink resistance this polymer covered the scale edges of the wool, whereas this did not occur with poly(hexafluoropropylene). [Pg.168]

The effect of reactive plasma and its distance form the PE film surface has also been studied in detail [138]. The surface of polyethylene films was modified with various water-soluble polymers [(poly[2-(methacryloy-loxy)ethyl phosphorylcholine] (PMPC), poly[2-(glucosyloxy)ethyl methacrylate] (PGEMA), poly(N-isopropylacrylamide) (PNIPAAm) and poly[N-(2-hy-droxypropyl) methacrylamide] (PHPMA)] using Ar plasma-post polymerisation technique [139]. Here, the reactive sites were generated on the PE surface under the influence of argon plasma. These reactive sites on the surface were then utilised to covalently anchor the functional monomers as shown in Scheme 11. [Pg.263]

In cases where control of molecular weight is important, for example in the use of dextran fractions as plasma expanders, a viscosity method is specified, for example, in the BP monograph. Staudinger proposed that the reduced viscosity of solutions of linear high polymers is proportional to the molecular weight of the polymer or its degree of polymerisation, p ... [Pg.283]


See other pages where Plasma polymerisation polymers is mentioned: [Pg.182]    [Pg.120]    [Pg.120]    [Pg.123]    [Pg.461]    [Pg.356]    [Pg.249]    [Pg.430]    [Pg.181]    [Pg.2]    [Pg.277]    [Pg.278]    [Pg.282]    [Pg.284]    [Pg.285]    [Pg.286]    [Pg.286]    [Pg.286]    [Pg.398]    [Pg.17]    [Pg.289]    [Pg.86]    [Pg.221]    [Pg.399]    [Pg.831]    [Pg.111]    [Pg.285]    [Pg.438]    [Pg.292]    [Pg.398]    [Pg.404]   
See also in sourсe #XX -- [ Pg.278 ]




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