Poly diameter

Capillary Tubes Figure 12.42 shows a cross section of a typical capillary tube. Most capillary tubes are made from fused silica coated with a 20-35-)J,m layer of poly-imide to give it mechanical strength. The inner diameter is typically 25-75 )J,m, which is smaller than that for a capillary GC column, with an outer diameter of 200-375 )J,m. 

Simha equation), where a/b is the length/diameter ratio of these cigarshaped particles. Doty et al.t measure the intrinsic viscosity of poly(7-benzyl glutamate) in a chloroform-formamide solution and obtained (approximately) the following results ... 

Plazek et al.t measured the viscosities of a poly(dimethyl siloxane) sample of = 4.1 X 10 over a range of temperatures using the falling-ball method. Stainless steel (P2 = 7.81 g cm" ) balls of two different diameters,... 

Suspension polymerization of VDE in water are batch processes in autoclaves designed to limit scale formation (91). Most systems operate from 30 to 100°C and are initiated with monomer-soluble organic free-radical initiators such as diisopropyl peroxydicarbonate (92—96), tert-huty peroxypivalate (97), or / fZ-amyl peroxypivalate (98). Usually water-soluble polymers, eg, cellulose derivatives or poly(vinyl alcohol), are used as suspending agents to reduce coalescence of polymer particles. Organic solvents that may act as a reaction accelerator or chain-transfer agent are often employed. The reactor product is a slurry of suspended polymer particles, usually spheres of 30—100 pm in diameter they are separated from the water phase thoroughly washed and dried. Size and internal stmcture of beads, ie, porosity, and dispersant residues affect how the resin performs in appHcations. 

Fig. 4. Surface of a polysulfone ultrafUtration hoUow-fiber membrane spun with poly-(vinylpyrrohdinone) (3). Surface pore diameter is 0.2—0.4 p.m.

Not in the class of digital recording storage media are video CDs with diameters of 200 and 300 mm, respectively. These are storage disks for recording the analogue signal of videos and are of air-sandwich constmction with two poly(methyl methacrylate) disks. 

Polymer—polymer iacompatibiHty encapsulation processes can be carried out ia aqueous or nonaqueous media, but thus far have primarily been carried out ia organic media. Core materials encapsulated tend to be polar soHds with a finite degree of water solubiHty. EthylceUulose historically has been the sheU material used. Biodegradable sheU materials such as poly(D,L-lactide) and lactide—glycoHde copolymers have received much attention. In these latter cases, the object has been to produce biodegradable capsules that carry proteias or polypeptides. Such capsules tend to be below 100 p.m ia diameter and are for oral or parenteral administration (9). 

In the suspension polymerization of PVC, droplets of monomer 30—150 p.m in diameter are dispersed in water by agitation. A thin membrane is formed at the water—monomer interface by dispersants such as poly(vinyl alcohol) or methyl cellulose. This membrane, isolated by dissolving the PVC in tetrahydrofuran and measured at 0.01—0.02-p.m thick, has been found to be a graft copolymer of polyvinyl chloride and poly(vinyl alcohol) (4,5). Early in the polymerization, particles of PVC deposit onto the membrane from both the monomer and the water sides, forming a skin 0.5—5-p.m thick that can be observed on grains sectioned after polymerization (4,6). Primary particles, 1 p.m in diameter, deposit onto the membrane from the monomer side (Pig. 1), whereas water-phase polymer, 0.1 p.m in diameter, deposits onto the skin from the water side of the membrane (Pig. 2) (4). These domain-sized water-phase particles may be one source of the observed domain stmcture (7). 

Fig. 6. Activation energy for diffusion in poly(vinyl chloride) as a function of penetrant mean diameter (19). To convert to cal, divide by 4.184.

Fig. 16. Diffusivities of penetrants in rigid (A) and plasticized ( ) poly(vinyl chloride) versus molecular diameter at 30°C (31).

Poly(vinyl chloride) is commercially available in the form of aqueous colloidal dispersions (latices). They are the uncoagulated products of emulsion polymerisation process and are used to coat or impregnate textiles and paper. The individual particles are somewhat less than 1 p,m in diameter. The latex may be coagulated by concentrated acids, polyvalent cations and by dehydration with water-miscible liquids. 

Smaller diameter columns are especially useful when expensive solvents are used. Figure 11.3 shows the analysis of poly (1,4-butylene terephthalate) using a Waters Alliance narrow-bore GPC system, quantitated against narrow polymethylmethacrylate standards. In this case, the solvent used is hexaflu-oro-2-isopropanol with 0.05 M sodium trifluoroacetic acid at a flow rate of... 

Figure 20 A typical scanning electron micrograph of the macroporous uniform poly(styrene-divinylbenzene) late> particles. Magnification 1200 x, (particle size = 16.0/rm average pore diameter = 200 nm).

Some authors have suggested the use of fluorene polymers for this kind of chromatography. Fluorinated polymers have attracted attention due to their unique adsorption properties. Polytetrafluoroethylene (PTFE) is antiadhesive, thus adsorption of hydrophobic as well as hydrophilic molecules is low. Such adsorbents possess extremely low adsorption activity and nonspecific sorption towards many compounds [109 111]. Fluorene polymers as sorbents were first suggested by Hjerten [112] in 1978 and were tested by desalting and concentration of tRN A [113]. Recently Williams et al. [114] presented a new fluorocarbon sorbent (Poly F Column, Du Pont, USA) for reversed-phase HPLC of peptides and proteins. The sorbent has 20 pm in diameter particles (pore size 30 nm, specific surface area 5 m2/g) and withstands pressure of eluent up to 135 bar. There is no limitation of pH range, however, low specific area and capacity (1.1 mg tRNA/g) and relatively low limits of working pressure do not allow the use of this sorbent for preparative chromatography. 

Analytical A proc is described for the quant titrimetric analysis of TeNMe in nitric acid (Ref 35)s and a spectrophotometric method is described in Ref 41 for the detn of small amts of TeNMe in air and w Critical Diameter. The crit diam for deton propagation of TeNMe thickened with poly-(methyl acrylate) and loaded with up to 75% inert solids was detd and found to decrease with increasing solids loading. It was postulated that the solids acted as reaction foci ahead of the deton front (Ref 45)... 

The next step is the hydrogen reduction of the trichlorosilane (Reaction 2 above). The end product is a poly crystalline silicon rod up to 200 mm in diameter and several meters in length. The resulting EGS material is extremely pure with less than 2 ppm of carbon and only a few ppb of boron and residual donors. The Czochralski pulling technique is used to prepare large single crystals of silicon, which are subsequently sliced into wafers for use in electronic devices.1 1... 

Poly(DL-lactide) was used as the excipient in microspheres of CCNU, a nitrosourea, prepared by a solvent evaporation procedure (96,97). PLA-CCNU microspheres 3.0 pm in diameter were injected i.v. and leukemia cell survival was determined by spleen colony assay. A 100-fold decrease in leukemia cell survival was observed with the microspheres in both spleen and liver compared to untreated controls. Promising results were also obtained with Lewis lung carcinoma in mice. These studies showed that 2- to 4-ym microspheres were preferentially targeted to the lungs. 

FIGURE 3 Release of -nitroaniline and the degradation of PCPA versus time. Disks (1.4 cm in diameter and 1 mm thick) of poly-(carboxyphenoxyacetic acid) (PCPA) were prepared containing 5% (w/w) -nitroaniline by compression molding, and degraded in 0.1 M pH 7.4 phosphate buffer at 37°C. The cumulative release of p-nitroaniline and degradation of PCPA were measured by absorbance at 380 and 235 nm, respectively. 

---