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Polyethylene surface treatment

Polyspend. [U.S. Cosmetics] Polyethylene surface treatment for cosmetics. [Pg.291]

An important newer use of fluorine is in the preparation of a polymer surface for adhesives (qv) or coatings (qv). In this apphcation the surfaces of a variety of polymers, eg, EPDM mbber, polyethylene—vinyl acetate foams, and mbber tine scrap, that are difficult or impossible to prepare by other methods are easily and quickly treated. Fluorine surface preparation, unlike wet-chemical surface treatment, does not generate large amounts of hazardous wastes and has been demonstrated to be much more effective than plasma or corona surface treatments. Figure 5 details the commercially available equipment for surface treating plastic components. Equipment to continuously treat fabrics, films, sheet foams, and other web materials is also available. [Pg.131]

Corrosion. Ammonium bifluoride dissolves in aqueous solutions to yield the acidic bifluoride ion the pH of a 5% solution is 3.5. In most cases, NH4HF2 solutions react readily with surface oxide coatings on metals thus NH4HF2 is used in pickling solutions (see Metal surface treatments). Many plastics, such as polyethylene, polypropylene, unplasticized PVC, and carbon brick, are resistant to attack by ammonium bifluoride. [Pg.148]

If corona, plasma, or flame treatment is chosen as the surface treatment, it is important to bond quickly after the treatment. Waiting several hours will reduce the effectiveness of the treatment. In some cases, attempts to bond 24 h after the treatment can give the same poor bonding results as if the plastic had never been surface treated. If surface oxidation is not possible, priming the surface with a chlorinated polyethylene primer is a second choice [95]. [Pg.809]

Figure 14 shows the ATR spectrum of the etched polyethylene surface treated with a chronic acid group [76]. Absorption bands due to surface treatment appear at 3300, 1700, 1260, 1215, and 1050 cm". The band at 3300 cm represents the absorption due to the hydroxyl group and that at 1700 cm " is due to the carbonyl group. The bands at 1260, 1215, and 1050 cm are all due to the alkyl sulfonate group. [Pg.827]

Nardin M. and Ward, I.M. (1987). Influence of surface treatment on adhesion of polyethylene fibers. Mater. Sci. Technol. 3, 814-826. [Pg.40]

This chapter is concerned primarily with the surface treatments of high performance fibers, including glass, carbon (or graphite), aramid, polyethylene... [Pg.171]

Fluorination of polyethylene surfaces leads to an increase in the surface energy, some degree of cross-linking and a reduction of the free volume of the polymer. All of these effects impart on the surface of the polymer a barrier that is very impermeable to hydrocarbon solvents. A blow-moulding process, in which a low concentration of fluorine in nitrogen is used as the blow-moulding gas, is used for the production of plastic fuel tanks for the automotive industry (Airopak , Air Products) [51]. Post-treatment of hydrocarbon surfaces with fluorine is an alternative technology and techniques for the surface fluorination of natural and synthetic rubber have been described [52]. [Pg.8]

Jickins R.S., Leonas K.K., Influence of a polyethylene glycol treatment on surface, hquid barrier and antibacterial properties Textile Chemist Colorist, 26 (12) (1994) 25-29. [Pg.241]

To further explore the influence of silica material properties (morphology, surface area, silanol concentration, and surface treatment) on the silica flame-retardant properties, various types of silicas (silica gel, fumed silicas, and fused silica) were investigated.50 51 Material properties of the various silicas are summarized in Table 8.6. These different types of silicas were added to polypropylene and polyethylene oxide to determine their flame-retardant effectiveness and mechanisms. Polypropylene was chosen as a non-char-forming thermoplastic, and polyethylene oxide was chosen as a polar slightly char-forming thermoplastic. Flammability properties were measured in the cone calorimeter and the mass loss rate was measured in the radiative gasification device in nitrogen to exclude any gas phase oxidation reactions. [Pg.199]

As an inorganic mineral, most unmodified nanoadditives are strongly hydrophilic and are generally compatible and miscible only with a few hydrophilic polymers, for instance, clay can only be made into PNs with polyethylene oxide),27 poly(vinyl alcohol),28 and a few other water soluble polymers. Most polymers are hydrophobic and thus they are neither compatible nor miscible with the unmodified nanoadditives, leading to an inability to achieve a PN with a good nanodispersion in most cases. Therefore, for most nanoadditives that have been used to prepare the PNs, an important and necessary feature is their surface treatment that provides compatibility to the nanoadditives and enables them to be uniformly dispersed (and/or separated into single nanoparticles) in the polymer matrix. [Pg.266]

For some plastics, surface treatments were necessary—for example, chromic acid treatment for polypropylene. When fillers were present in the plastics the results with cyanoacrylates often were better (this was apparent in particular with polyethylene). [Pg.106]

So far, emphasis has been placed on the treatment of polyolefins to improve printability, but the same treatments affect also other processes. As an example, while an untreated polyethylene surface will not retain an adhesive the treated and modified surfaces are receptive to adhesives. A field of increasing importance for packaging is the production of laminates of film with other materials and, as examples, suitably pre-treated polyethylene film can be bonded securely to substrates such as cellulose or polyester films and aluminium foil, using standard adhesives, whereas this cannot be achieved without pre-treatment. [Pg.225]

Since slower-curing epoxy adhesives systems flow over and wet high-energy surfaces very well, there is little chance for air to become trapped at the interface. As a result, mechanical abrasion is often recommended as a substrate surface treatment prior to application of the epoxy adhesive. The added surface area and the mechanical bonding provided by the additional peaks and valleys on the surface will enhance adhesive strength. If the adhesive does not wet the substrate surface well, such as in the case of epoxy resin on polyethylene, mechanical abrasion is not recommended since it will only encourage the probability of gas voids being trapped at the interface. [Pg.56]

To obtain a usable adhesive bond with polyolefins, the surface must be treated. A number of surface preparation methods, including flame, chemical, plasma, and primer treatments, are in use. Figure 16.4 illustrates the epoxy adhesive strength improvements that can be made by using various prebond surface treatments to change the critical surface tension of polyethylene. [Pg.372]

Polyethylene terephthalate cannot be solvent-cemented or heat-welded. Adhesives are the prime way of joining PET to itself and to other substrates. Only solvent cleaning of PET surfaces is recommended as a surface treatment. The linear film of polyethylene terephthalate (Mylar) provides a surface that can be pretreated by alkaline etching or plasma for maximum adhesion, but often a special treatment such as this is not necessary. An adhesive for linear polyester has been developed from a partially amidized acid from a secondary amine, reacted at less than stoichiometric with a DGEB A epoxy resin, and cured with a dihydrazide.72... [Pg.375]

Surface treatments consist of washing with solvent, abrading, or, in the most demanding applications, cyclizing with acid. The most common elastomers to be bonded in this way include nitrile, neoprene, urethane, natural rubber, SBR, and butyl rubber. It is more difficult to achieve good bonds with silicones, fluorocarbons, chlorosulfonated polyethylene, and polyacrylate. [Pg.383]

Untreated polyethylene (molded against PTFE) (no surface treatment)... [Pg.156]

Marlex 5003 polyethylene crystallized from 0.04% solution in xylene at 85°C. then molded into 10 mil. sheets at 160°C. No surface treatment A—Polyethylene film (untreated) exposed to vapors of a boiling 1.1 hexane, heptane mixture for 5 minutes A—Polyethylene film (untreated) irradiated with a Van de Graaff generator to a dose of 10 Mrads O—Polyethylene film exposed to glass cleaning solution at 80°C. for 4 minutes... [Pg.156]

Sprang N, Theirich D, and Engemann J. Plasma and ion beam surface treatment of polyethylene. Surf. Coat. Technol. 1995 74—75 689-695. [Pg.59]


See other pages where Polyethylene surface treatment is mentioned: [Pg.497]    [Pg.87]    [Pg.295]    [Pg.809]    [Pg.530]    [Pg.220]    [Pg.3]    [Pg.37]    [Pg.187]    [Pg.169]    [Pg.237]    [Pg.258]    [Pg.264]    [Pg.134]    [Pg.792]    [Pg.185]    [Pg.373]    [Pg.381]    [Pg.148]    [Pg.155]    [Pg.157]    [Pg.136]    [Pg.210]    [Pg.79]    [Pg.178]    [Pg.259]    [Pg.70]    [Pg.297]    [Pg.116]   


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