Polymethylmethacrylate particles

Figure 7.24 Shear stress versus shear rate for dispersions in water of polymethylmethacrylate particles with radius a = 220 nm and volume fraction (f> = 0.070 at ionic strength 0.02 g ions/liter of NaCl and zeta potentials of +14.6 m. -1-21.6 (21 -1-29.3 (31. 3-35.9 (4), -1-55 (5), and supernatant (6). (From Friend and Hunter 1971, reprinted with permission from Academic Press.)...

Dinsmore and Weitz (2002) [60] examined a model system of polymethylmethacrylate particles dyed with rhodamine in a density- and refractive-index-matched solution of decalin and cyclohexylbromide. They used CLSM to follow the (very slow) aggregation in real time and determined the particle positions in full three-dimensional detail. From this they performed a comprehensive structural analysis of the gels, including measurement of coordination numbers and backbone fractal dimension of the structures, as well as the much more commonly measured mass fractal dimension. 

One of the methods of obtaining printable film is based on the use of solid antiblock, as discussed below. The solid antiblocks are such that they do not break up when subjected to mechanical stress. Suitable antiblocks include fully crosslinked or non-meltable polysiloxane, polymethylmethacrylate particles such as Epo-... 

Organic solvents are most commonly used, and encapsulating polymers include ethylcellu-lose, NC, polvvinylidene chloride, polystyrene, polycarbonate, polymethylmethacrylate, polyvinyl acetate and others. Inter facial polymerization produces a polymer such as nylon at the interface between layered solns of two precursor materials such as (in the case of a nylon) a diamine and a diacid (Refs 3 11). If the particle or drop-... 

Preparation of nanoparticles can be by a variety of different ways. The most important and frequently used is emulsion polymerization others include interfacial polymerization, solvent evaporation, and desolvation of natural proteins. The materials used to prepare nanoparticles are also numerous, but most commonly they are polymers such as poly-alklcyanoacrylate, polymethylmethacrylate, poly-butylcyanoacrylate, or are albumin or gelatin. Distribution patterns of the particles in the body can vary depending on their size, composition, and surface charge [83-85]. In particular, nanoparticles of polycyanoacrylate have been found to accumulate in certain tumors [86,87]. 

Polymeric particles can be constructed from a number of different monomers or copolymer combinations. Some of the more common ones include polystyrene (traditional latex particles), poly(styrene/divinylbenzene) copolymers, poly(styrene/acrylate) copolymers, polymethylmethacrylate (PMMA), poly(hydroxyethyl methacrylate) (pHEMA), poly(vinyltoluene), poly(styrene/butadiene) copolymers, and poly(styrene/vinyltoluene) copolymers. In addition, by mixing into the polymerization reaction combinations of functional monomers, one can create reactive or functional groups on the particle surface for subsequent coupling to affinity ligands. One example of this is a poly(styrene/acrylate) copolymer particle, which creates carboxylate groups within the polymer structure, the number of which is dependent on the ratio of monomers used in the polymerization process. 

Kreuter and Speiser [77] developed a dispersion polymerization producing adjuvant nanospheres of polymethylmethacrylate) (PMMA). The monomer is dissolved in phosphate buffered saline and initiated by gamma radiation in the presence and absence of influenza virions. These systems showed enhanced adjuvant effect over aluminum hydroxide and prolonged antibody response. PMMA particles could be distinguished by TEM studies and the particle size was reported elsewhere to be 130 nm by photon correlation spectroscopy [75], The particle size could be reduced, producing monodisperse particles by inclusion of protective colloids, such as proteins or casein [40], Poly(methylmethacrylate) nanoparticles are also prepared... 

This was corroborated by experimental results obtained in single particle experiments carried out for polypropylenes. It was possible to show that the relative attrition behavior under pure sliding friction stresses was identical to that observed in a pipe bend whereas deviations to that under pure normal impact conditions were found. For polymethylmethacrylate and polystyrene on the other hand, the relative attrition behavior in the pipe bend corresponds to that of the normal impact experiments. 

Data from a number of different particle size analysis instrumental methods including light scattering, field flow fractionation, hydrodynamic chromatography and microscopy were obtained for a series of polymethylmethacrylate latexes and were compared to DCP results (2). These and other comparative results have demonstrated the accuracy of the instrument and method. The reproducibility and precision of the instrument also were studied and are reported elsewhere ( 1 ). 

The other kind of systems largely studied, consists of polymethylmethacrylate (PMMA) or silica spherical particles, suspended in organic solvents [23,24]. In these solvents Q 0 and uy(r) 0. The particles are coated by a layer of polymer adsorbed on their surface. This layer of polymer, usually of the order of 10-50 A, provides an entropic bumper that keeps the particles far from the van der Waals minimum, and therefore, from aggregating. Thus, for practical purposes uw(r) can be ignored. In this case the systems are said to be sterically stabilized and they are properly considered as suspensions of colloidal particles with hard-sphere interaction [the pair potential is of the form given by Eq. (5)]. 

The first step was to spin-coat an electron-sensitive polymer (polymethylmethacrylate (PMMA)) onto an oxidized Si(l 00) wafer (which serves as a Si02 support). The desired pattern is subsequently written into the polymer layer by a highly collimated electron beam, followed by the selective dissolution of the polymer damaged by the electron exposure. A thin film of platinum is then deposited on this mask, and after the remaining polymer resist is removed completely by dissolution, metal particles remain on the substrate and are located at the positions of the prior electron irradiation, typically forming an ordered array of nanoparticles. 

Brendle described a process which he called polymer grafting, in which particles of molybdenum disulphide or other solid lubricants were coated with various polymers, including polystyrene, polymethylmethacrylate and poly-isobutylvinyl ether. The process was most conveniently carried out by grinding coarse molybdenum disulphide powder in a 20% - 30% solution of the appropriate monomer in a solvent. The quantity of polymer added to the molybdenum disulphide particles was very small, and could not be detected by scanning electron microscopy or infrared spectroscopy. The carbon content (1-4%) indicated a polymer content up to 6% maximum. Brendle considered that the polymer was preferentially grafted onto surface freshly exposed by grinding. This may be partly true, but in view of later... 

C. Parkinson et al. (17) considered the effect of particle size distribution on viscosity. They studied suspensions of polymethylmethacrylate) spheres in Nujol with diameters of 0.1, 0.6, 1.0 and 4.0 microns with different volume fractions and with different particle size combinations to determine the influence of size-distribution on the viscosity. Each particle size gave a certain contribution to the final viscosity based on the volume fraction and the hydrodynamic coefficient obtained from the empirical equation for that particle size. The contributions were expressed in the same form as in Mooney s model, and the viscosity was calculated from the product of each term, n... 

Figure 420. Coating of spherical polymethylmethacrylate (PMMA) particles with titanium oxide (Ti02) by Mechanofusion. (Courtesy of Hosokawa Micron Corp., Osaka, Japan.) (a) Raw materials before treatment. PMMA 5 /tm, Ti02 0.015 /tm (somewhat naturally agglomerated), (b) Treated product particles...

Steric stabilization is another well-established method of stabilizing colloidal suspensions of submicron to micron size [23]. The particles are coated with a layer of adsorbed or grafted polymer chains that provides a steric repulsion of entropie origin and helps disperse the particles by counterbalancing van der Waals attraction (Fig. la). The polymeric nature of the adsorbed or grafted layer softens the interparticle interactions and makes the particles intrinsically deformable. Many polymer chain/particle combinations have been synthesized and studied, and are described in the literature. Several popular colloidal systems consist of silica particles covered with various polymers such as polydimethylsiloxane [24], stearyl alcohol [25], alkyl chains [26], and polyethylene oxide [27]. Polymethylmethacrylate and polystyrene particles grafted with polymer chains have also been used extensively. For a review on the impressive literature on the subject we refer the interested reader to Vlassopoulos and Fytas [2]. 

Cement is a binder that sets and hardens by itself or binds other materials together. The most widely known application of cements is in construction a second one is the area of bone cements. Cements used in construction are characterized as hydraulic or nonhydraulic and mostly for the production of mortars and concrete. Hydraulic cements set and harden after combining with water. Most construction cements are hydraulic and based on Portland cement, which consists of calcium silicates (at least 2/3 by weight). Nonhydraulic cements include the use of nonhydraulic materials such as lime and gypsum plasters. Bone cements and bone cement composites refer to compounds that have a polymer matrix with a dispersed phase of particles. For instance, polymethylmethacrylate (PMMA) is reinforced with barium sulphate crystals (for radio-opacity) or with hydroxyapatite... 

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