Polymethyl methacrylate surface

Perfluoroalkyl chain surfactants are much poorer wetting agents than alkyl chain surfactants for both paraffin and polymethyl methacrylate surfaces (Pyter, 1982). One explanation may be the mutual phobicity of alkyl and perfluoroalkyl chains, causing perfluoroalkyl chain surfactants to be adsorbed more poorly than alkyl chain surfactants at these solid-aqueous solution interfaces. 

The main experimental techniques used to study the failure processes at the scale of a chain have involved the use of deuterated polymers, particularly copolymers, at the interface and the measurement of the amounts of the deuterated copolymers at each of the fracture surfaces. The presence and quantity of the deuterated copolymer has typically been measured using forward recoil ion scattering (FRES) or secondary ion mass spectroscopy (SIMS). The technique was originally used in a study of the effects of placing polystyrene-polymethyl methacrylate (PS-PMMA) block copolymers of total molecular weight of 200,000 Da at an interface between polyphenylene ether (PPE or PPO) and PMMA copolymers [1]. The PS block is miscible in the PPE. The use of copolymers where just the PS block was deuterated and copolymers where just the PMMA block was deuterated showed that, when the interface was fractured, the copolymer molecules all broke close to their junction points The basic idea of this technique is shown in Fig, I. 

All of the eommereial alkyl eyanoaerylate monomers are low-viseosity liquids, and for some applications this can be an advantage. However, there are instances where a viseous liquid or a gel adhesive would be preferred, sueh as for application to a vertical surface or on porous substrates. A variety of viscosity control agents, depending upon the desired properties, have been added to increase the viscosity of instant adhesives [21]. The materials, which have been utilized, include polymethyl methacrylate, hydrophobic silica, hydrophobic alumina, treated quartz, polyethyl cyanoacrylate, cellulose esters, polycarbonates, and carbon black. For example, the addition of 5-10% of amorphous, non-crystalline, fumed silica to ethyl cyanoacrylate changes the monomer viscosity from a 2-cps liquid to a gelled material [22]. Because of the sensitivity of cyanoacrylate esters to basic materials, some additives require treatment with an acid to prevent premature gelation of the product. 

Liu and Rauch (2003) of Motorola investigated oligonucleotide probe attachment onto polystyrene (PS), polycarbonate (PC), polymethyl methacrylate (PMMA), and polypropylene (PP) plastic surfaces. They utilized three different immobilization processes SurModics surface modification solution (that allows attachment of adsorbed reactive groups to a surface by photoactivation of polymers at 254 nm). Pierce Reactive-Bind coating solution, and CTAB (cetyltrimethylammonium bromide, a cationic detergent). Not surprisingly, the microarray performances on these plastics varied. 

Uses. Production of polymethyl methacrylate polymers for use in acrylic sheet and acrylic molding, extrusion powder, acrylic surface coatings, printing inks, and adhesives used in surgery and dentistry... 

It appears from these data that adsorption to hydrophilic surfaces would be a viable strategy. Other research produced a similar conclusion. Waugh et al. showed that prothrombin (another member of the coagulation cascade) binds more strongly to polymethyl methacrylate than glass, ("hating showed that plasma proteins bind more strongly to polyvinyl chloride than a hydrophilic dialysis membrane. 

Controlled grafting via heterogeneous ATRP of polymethyl methacrylate onto poly(ethylene-co-styrene) is one of the most significant advancements in the surface modification of PE [199]. The grafting of PMMA was carried out in presence of CuBr and pentamethyldiethylenetriamine as a catalyst via the well-known ATRP mechanism, as shown in Scheme 13. 

Polyacrylic acid stabilised latices have been prepared by aqueous dispersion polymerisation. The method used is analogous to the non-aqueous dispersion (NAD) polymerisation methods originally used to prepare polymethyl methacrylate particles in aliphatic hydrocarbons (1. In effect the components of a NAD polymerisation have been replaced as follows aliphatic hydrocarbon by aqueous alcohol, and degraded rubber, the stabiliser, by polyacrylic acid (PAA). The effect of various parameters on the particle size and surface charge density of the latices is described together with details of their colloidal stability in the presence of added electrolyte. 

The acrylic plastics use the term acryl such as polymethyl methacrylate (PMMA), polyacrylic acid, polymethacrytic acid, poly-R acrylate, poly-R methacrylate, polymethylacrylate, polyethylmethacrylate, and cyanoacrylate plastics. PMMA is the major and most important homopolymer in the series of acrylics with a sufficient high glass transition temperature to form useful products. Repeat units of the other types are used. Ethylacrylate repeat units form the major component in acrylate rubbers. PMMAs have high optical clarity, excellent weatherability, very broad color range, and hardest surface of any untreated thermoplastic. Chemical, thermal and impact properties are good to fair. Acrylics will fail in a brittle manner, independent of the temperature. They will suffer crazing when loaded at stress about halfway to the failure level. This effect is enhanced by the presence of solvents. 

Polysulfone membranes were prepared from 12.5, 13.75, and 15% (wt. %) polysulfone solution in dimethylformamide and formed on the surface of porous, sintered polymethyl methacrylate bars. An effective surface of each membrane was 49.2 cm. The effect of some casting parameters (composition and the temperature of the casting solution, time of solvent evaporation) and the pressure applied on the transport and separation properties of the membranes were analyzed. The experiments were carried out in a 1.2 dm pressure apparatus with continuous circulation of the permeate between feeding tank and the apparatus. It was found that membranes cast from 12.5% polysulfone solution of a temperature of 298 K with no solvent evaporation displayed the best properties. After 160 hours of operation at 0.18 MPa, the membranes in question showed an ability of a 97 to 99% rejection of 781.2 molecular-weight dye. The volume flux of the dye solution varied from 0.6 to 0.8m /m per day. 

Polysulfone membranes cast on the surface of sintered polymethyl methacrylate bars may be applied to the decolorization of aqueous solutions by ultrafiltration... 

Unlike their parent product, powder cleansers, the cream cleansers usually use the gentler calcite abrasive. This, combined with their liquid form, helps to convey the image of less harsh cleaning to the consumer. This is especially important to consumers who have softer, plastic surfaces in their bathrooms such as the fiberglass (polymethyl methacrylate) shower enclosures which are much more easily marred than the traditional vitreous materials [18]. 

FIGURE 6-7 Plots of adhesion tension (yi4 cos 0) versus surface tension (y/4) for surfactant solutions on different substrates DE, paraffin in the presence of air FG, Teflon in the presence of air HJ, paraffin or Teflon in the presence of mineral oil (plot of yL0 cos 0 versus yLO), KL, anionic surfactant solution on nylon or polymethyl methacrylate in the presence of air MN, mineral in the presence of air. 

Tphe surface activity of block copolymers containing dimethylsiloxane units as one component has received considerable attention. Silicone-poly ether block copolymers (1,2,3) have found commercial application, especially as surfactants in polyurethane foam manufacture. Silicone-polycarbonate (4, 5), -polystyrene (6, 7), -polyamide (8), -polymethyl methacrylate (9), and -polyphenylene ether (10) block copolymers all have surface-modifying effects, especially as additives in other polymeric systems. The behavior of several dimethylsiloxane-bisphenol A carbonate block copolymers spread at the air—water interface was described in a previous report from this laboratory (11). Noll et al. (12) have described the characteristics of spread films of some polyether—siloxane block co-... 

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