Polymer blends with poly

Park et al, reported the synthesis and application of terpolymer bearing cyclic carbonate and cinnamoyl groups. The syntheses of photopolymer with pendant cinnamic ester and cyclic carbonate groups was achieved by the addition reaction of poly(glycidyl methacrylate-co-styrene) with CO2 and then with cinnamoyl chloride. Quaternary ammonium salts showed good catalytic activity for this synthesis. Photochemical reaction experiments revealed that terpolymer with cinnamate and cyclic carbonate groups has good photosensitivity, even in the absence of sensitizer. In order to expand the application of the obtained terpolymer, polymer blends with poly(methyl methacrylate) were also prepared. 

Goh, Paul, and Barlow [10] found that an alpha-methylstyrene-acrylonitrile (AMS-AN) copolymer at 50 mole fraction AN formed miscible polymer blends with poly(methyl methacrylate) (PMMA) and with poly(ethyl methacrylate) (PEMA). AMS-AN copolymer did not form miscible blends with polyacrylates or polyvinyl acetate. The miscible blends were found to exhibit lower critical solution temperature (LCST) behavior. 

Also, PBT is blended with poly(ethylene terephthalate) (PET), polysulfone, and SMA (303). PET may also be blended with a number of other engineering polymers, such as PC and impact modifiers. 

The effect of a second polymer blended with PPS which causes enhanced nucleation of PPS has been previously observed. It was found that low concentrations (1—2 wt %) of poly(phenylene sulfide ketone) and poly(ether ether ketone), when melt-blended with PPS, function effectively to increase the nucleation density of PPS (149). 

Blends with PVC. Nitrile mbber may be blended with poly(vinyl chloride) (PVC) by the polymer producer by two different techniques (1) blending of NBR latex with PVC latex followed by co-coagulation and drying, or (2) physically mixing the soHd NBR and PVC powder in mixing equipment such as an internal mixer. NBR—PVC polymer blends are well known for the good ozone resistance that is imparted by the PVC. 

Some preliminary results indicate that the functionalized polymers form miscible blends with poly(methyl methacry1 ate). 

Hybrid organic-inorganic polymer-polymer composites were prepared by blending with poly(A-vinylpyrrolidone) (PVPr), poly(4-vinylpyridine) (PVPy) and poly(ethyl oxazoline) (PEOx). It was found that the properties of these hybrids depended strongly on the preparation conditions.14... 

The end groups of a PDMS polymer have been shown to affect the interfacial tension of blends with poly(butadiene)126. Thus, substitution of an amine-terminated PDMS for a trimethylsilyl-terminated PDMS can reduce the interfacial tension by up to 30%. This effect is postulated to arise due to the amine end group having a surface energy closer to that of butadiene than does the trimethylsilyl group and thus being present at the interface. 

Examples of known phosphazene polymer blends are those in which phosphazenes with methylamino, trifluoroethoxy, phenoxy, or oligo-ethyleneoxy side groups form blends with poly(vinyl chloride), polystyrene, poly(methyl methacrylate), or polyethylene oxide).97 100 IPNs have been produced from [NP(OCH2CH2OCH2CH2OCH3)2] (MEEP) and poly(methyl methacrylate).101-103 In addition, a special type of IPN has been reported in which a water-soluble polyphosphazene such as MEEP forms an IPN with a silicate or titanate network generated by hydrolysis of tetraethoxysilane or tetraalkoxytitanane.104 These materials are polyphosphazene/ceramic composites, which have been described as suitable materials for the preparation of antistatic layers in the manufacture of photographic film. 

Miyashita et al. carried out miscibility characterization of CA blends with poly(N-vinyl pyrrolidone) (PVP), poly(vinyl acetate) (PVAc), and poly(N-vinyl pyrrolidone-co-vinyl acetate) random copolymers [P(VP-co-VAc)s] [ 104]. On the basis of thermal transition data obtained by differential scanning calorimetry (DSC), a miscibility map (Fig. 8) was completed as a function of the degree of substitution (DS) of CA and the VP fraction in P(VP-co-VAc). Figure 9 compares results of the DSC measurements between two blending pairs of CA/P(VP-co-VAc) corresponding to the polymer combinations marked as A and B in Fig. 8. In the data (Fig. 9b) for the blends of CA (DS = 2.95) with P( VP-co-VAc) of VP = 51 mol %, we can readily see a sign of poor miscibility, as is evidenced from the lack of an appreciable shift in the... 

Poly(glycolic acid) and poly(3-HB) form immiscible blends with poly(e-CL). Poly(3-HB) is an expensive polymer, which crystallizes slowly from the melts and embrittles on ageing. Poly(e-CL), on the other hand, has a low mp and limited use. An optimal combination of cost and properties may be obtained by blending [114]. 

Poly-e-caprolactone designated as PCL-700 was supplied by J. V. Koleske of the Union Carbide Corp. This polymer has been used in several other blend studies (1-6). The polymers blended with PCL were poly (vinyl chloride) (PVC) and nitrocellulose (NC). The poly-... 

In the case of polystyrene blends with poly(vinyl methyl ether) two phase behaviour was found for blends from various chlorinated solvents whereas single phase behaviour was found for blends from toluene The phase separation of mixtures of these polymers in various solvents has been studied and the interaction parameters of the two polymers with the solvents measured by inverse gas chromatography It was found that those solvents which induced phase separation were those for which a large difference existed between the two separate polymer-solvent interaction parameters. This has been called the A% effect (where A% = X 2 Xi 3)-A two phase region exists within the polymer/polymer/solvent three component phase diagram as shown in Fig. 2. When a dilute solution at composition A is evaporated, phase separation takes place at B and when the system leaves the two phase region, at overall... 

Nakatsuka S, Andrady LA. Permeability of vitamin-B-12 in chitosan membranes effect of crosslinking and blending with poly(vinyl alcohol) on permeability. ] Appl Polym Sci 1992 44 7-28. 

Some studies show that pyrolysis of certain polymer blends can be influenced by the migration of a small molecule or a small radical formed from one type of polymer and affecting the other type. For example, poly(methyl methacrylate) (PMMA) in blends with poly(vinyl chloride) (PVC) shows higher resistance to heat. The thermal decomposition of PVC generates HCI, which interacts with the PMMA forming anhydride units in the middle of PMMA chains, as shown below ... 

IGC was used to determine the thermodynamic miscibility behavior of several polymer blends polystyrene-poly(n-butyl methacrylate), poly(vinylidene fluoride)-poly(methyl methacrylate), and polystyrene-poly(2,6-dimethyl-1,4-phenylene oxide) blends. Specific retention volumes were measured for a variety of probes in pure and mixed stationary phases of the molten polymers, and Flory-Huggins interaction parameters were calculated. A generally consistent and realistic measure of the polymer-polymer interaction can be obtained with this technique. 

Lim, S.K. Kim, J.W. Chin, L Kwon, Y.K. Choi, H.J. Preparation and interaction characteristics of organically modified montmorillonite nanocomposite with miscible polymer blend of poly(ethylene oxide) and poly(methyl methacrylate). Chem. Mater. 2002, 14, 1989-1994. 

In blends composed of immiscible polymers, amorphous polymer does not affect the crystallization of crystallizable polymer, but if two polymers are miscible, amorphous polymer acts as diluent and affects crystallization of the second polymer. Poly(E-caprolactone) is a crystallizable component of the blend with poly( vinyl butyral), which is studied in compositions containing carbon black. Typically, blends of these two polymers form very large spherulites, and it is interesting to find out how carbon black affects crystallization and other properties of the blend as well as the distribution of carbon black in relationship to the spherulites. Figure... 

MacKnight and coworkers found that several poly(imide)s, such as Ultem poly(ether imide) and XU218 poly(imide), formed miscible blends with poly (benzimidazole) (FBI) [58, 59]. The miscibility of these blends is believed to result from specific interactions between the benzimide ring of the poly(im-ide) and benzimidazole ring of FBI. In a later study, Grobelny et al. [60] reported the CFMAS spectra of several of these blends. Slight changes in the lineshape were observed in the intimate blends, and seen as evidence of the specific interactions between the polymers. In particular, the peak in the spectra, due to the imide carbonyl carbon, was seen to broaden towards... 

De Paoli and coworkers7 have used the more soluble poly(o-methoxyaniline) doped with p-toluene sulfonic acid to prepare a composite blend with poly(epichlorohydrin-co-ethylene oxide), but conductivities were relatively low (10-3 S cm-1) even with a high 50% (w/w) conducting polymer loading. 

As outlined in the previous section, the good charge storage of the binary PPE/PS blends was in part attributed to the proposed presence of heterogeneities in the polymer bulk. In this section, heterogeneities are further introduced by adding a third component, namely the triblockcopolymer poly(styrene-Msobutylene-fe-styrene) (SIBS) to form ternary polymer blends with PPE and PS [65], The chemical struc-... 

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