Solid-phase prepared poly ethylene

Several SP materials have been used for the extraction of FRs from aqueous samples, plasma and milk (Table 31.7). Similar materials have been used for all FRs. Typical SP materials include Ci8 and Cg bonded to porous silica, highly cross-linked poly(styrene divinylbenzene) (PS-DVB), and graphitized carbon black (GCB). It is also possible to use XAD-2 resin for extraction of various FRs, pesticides, and plastic additives from large volumes of water (100 1). The analytes can then be either eluted from the resin by acetone hexane mixture, or Soxhlet extracted with acetone and hexane. For a specific determination of diphenyl phosphate in water and urine, molecularly imprinted polymers have been used in the solid phase extraction. The imprinted polymer was prepared using 2-vinylpyridine as the functional monomer, ethylene glycol dimethacrylate as the cross linker, and a structural analog of the analyte as the template molecule. Elution was done with methanol triethylamine as solvent. Also solid phase microextraction (SPME) has been applied in the analysis of PBDEs in water samples. The extraction has been done from a headspace of a heated water sample (100°C) using polydimethylsiloxane (PDMS) or polyacryl (PA) as the fiber material. ... 

Another example is work by Bradley and coworkers who incorporated short oligomer (polyethylene glycol) groups into the backbone of the cross-linked polystyrene [11]. The oligomer poly (ethylene glycol) in this preparation also acts as a spacer to separate the polystyrene backbone from locations of the reactions. The material was used efficiently in a solid phase peptide synthesis. 

The freeze fracture method has been used to study the structure of colloidal particles in water-oil mixtures stabilized by polymer emulsifiers. Microemulsions consisting of water, toluene and graft copolymer composed of a polystyrene backbone and a poly(ethylene oxide) graft were deposited onto a small gold plate, quenched in liquid nitrogen in equilibrium with its own solid phase [436]. Replicas of the fractured surfaces were washed with tetrahydrofuran, which showed the micellar structure of the copolymers. A similar method was used for the preparation of polystyrene polymer latexes for TEM study of the size distribution [437]. In this case, the frozen droplet was microtomed, with a cold knife at -100 to -120°C, etched for up to 90 s and then a platinum-carbon replica was prepared. Etching was found to be unnecessary and a potential cause of error. The remaining latex was dissolved away before examination of the replica. Such replicas can reveal the size distribution and structure of the latex particles. 

Frechet and coworkers explored the synthesis of polyester dendrons on solid support. These dendrons, based on 2,2-bis(hydroxymethyl)propanoic acid monomers, were assembled up to the fourth generation on poly(2-hydroxyethyl methacrylate-co-ethylene dimethacrylate) resin and decorated with chiral proline derivatives (Scheme 15.15). T vo methods for preparation of these materials were reported. The solid-phase divergent approach yielded polymer with higher loading but a less precise architecture than the second approach. The second approach, the divergent synthesis of the dendrons in solution, followed by the focal point deprotection and then attachment to the solid support, led to well-defined structures on the polymer, but relatively low loading. 

Poly(ethylene glycol) can act as both a reductant and carbon source. Compared with traditional solid-state reactions, the prepared LiFeP04/C composite has a better crystal phase, and its particle size ranges from several nanometers to several hundred nanometers. The particles are connected by a netlike carbon structure to form secondary particles. The reversible capacity is around 157 mAh/g at 0.1 C rate. No ball-milling, preparation of intermediates, presintering, or postdeposition treatment is needed. 

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