Composites Crystallisation

These materials, as described in Table 2, were prepared at different compositions, crystallisation temperatures and autoclave types conditions which give rise to unique NU-85 materials in terms of the xrd line intensity. 

To illustrate the observed changes in conductivity and pH during the composite PCC production (c-PCC), colloidal PCC composite crystallisation is shown in Fig. 5.4. The following mechanism can be proposed, similar to precipitation of PCC... 

Virgin and recycled polyethylene terephthalate (PET) was blended with polyether-imide (PEI) in proportions between 0 and 50 percent PEI content and samples were examined by differential scaiming calorimetry and Fourier transform infrared spectroscopy. All blends were completely miscible, as indicated by a single glass transition temperature which is dependent on blend composition. Crystallisation rates of PET were retarded strongly at 20 percent PEI content and above, but degree of crystallinity was easily determined from a linear correlation between a structural parameter measured spectroscopically and enthalpy of fusion. Trans conformer activation energy measurement confirmed the effects of PEI content on crystallisation of PET. 9 refs. 

Crystalline TSP is a dodecahydrate with somewhat variable composition between the limits of (Na PO I2H2O) 0.25NaOH and (Na PO I2H2O) l/TNaOH. It is manufactured by crystallisation below 60°C from a solution with an Na20/P20 mole ratio slightly lower than 3.25. Crystals are isolated by centrifugation and air-dried at ca 40°C to minimise dehydration. 

The clear supernatant solution is decanted and sold in Hquid form or concentrated to approximately 61.5 ° Bh and then allowed to soHdify to form blocks that are cmshed, ground, and graded. A typical analysis for the dry product is total A117.0—17.5% Fe202 <0.5% water of composition 42—43% insoluble <1.0%. Liquid alum contains 7.5—8.5% Al O. At concentrations >8.5% AI2O2, crystallisation of the solution may occur. 

Commercially, the PMDA mixtures are normally treated with phosgene to produce the corresponding isocyanates. These isocyanate mixtures, commonly called polymeric MDI (PMDI), are sold direcdy and have varied chemical compositions. The 4,4 -MDI can be separated from the PMDI products by distillation or crystallisation (31,32). The amount of 4,4 -MDI that is removed depends on marketing conditions. The residues are also viable commercial products. 

The maximum rates of crystallisation of the more common crystalline copolymers occur at 80—120°C. In many cases, these copolymers have broad composition distributions containing both fractions of high VDC content that crystallise rapidly and other fractions that do not crystallise at all. Poly(vinyhdene chloride) probably crystallises at a maximum rate at 140—150°C, but the process is difficult to foUow because of severe polymer degradation. The copolymers may remain amorphous for a considerable period of time if quenched to room temperature. The induction time before the onset of crystallisation depends on both the type and amount of comonomer PVDC crystallises within minutes at 25°C. 

Calcium siHcate hydrate is not only variable ia composition, but is very poody crystallised, and is generally referred to as calcium siHcate hydrate gel or tobermorite gel because of the coUoidal sizes (<0.1 fiva) of the gel particles. The calcium siHcate hydrates ate layer minerals having many similarities to the limited swelling clay minerals found ia nature. The layers are bonded together by excess lime and iatedayer water to form iadividual gel particles only 2—3 layers thick. Surface forces, and excess lime on the particle surfaces, tend to bond these particles together iato aggregations or stacks of the iadividual particles to form the porous gel stmcture. 

Poly(phenylene sulfide) (PPS) is another semicrystalline polymer used in the composites industry. PPS-based composites are generally processed at 330°C and subsequently cooled rapidly in order to avoid excessive crystallisation and reduced toughness. The superior fire-retardant characteristics of PPS-based composites result in appHcations where fire resistance is an important design consideration. Laminated composites based on this material have shown poor resistance to transverse impact as a result of the poor adhesion of the fibers to the semicrystalline matrix. A PPS material more recently developed by Phillips Petroleum, AVTEL, has improved fiber—matrix interfacial properties, and promises, therefore, an enhanced resistance to transverse impact (see PoLYAffiRS containing sulfur). 

The copolymers are prepared using a mixture of dimethyl terephthalate and dimethyl naphthalate. Published data indicates a reasonably linear relationship between and copolymer composition on the lines discussed in Section 4.2, e.g. Tg for a 50 50 copolymer is about 100°C which is about mid-way between Tg figures for the two homopolymers. In line with most other copolymers there is no such linearity in the crystalline melting point (T, ). As comonomer levels are introduced drops from the values for both homopolymers and indeed crystallisation only readily occurs where one of the components is dominant, i.e. 80%. Thus commercial copolymers are usually classified into two types ... 

Worenine. This alkaloid, also obtained by Kitasato from Coptis japonica was isolated as the tetrahydro-base, C,oHjg04N, which crystallises from alcohol in colourless prisms, m.p. 212-3°, and is oxidised by iodine in alcohol to worenine iodide, yellow crystals from which worenine chloride, thin orange-yellow prisms, m.p. 295° (dec.), can be obtained. Tetrahydro-worenine behaves as a tertiary base, contains methylenedioxy- but no methoxyl groups, and its absorption spectrum closely resembles that of tetrahydrocoptisine from which it differs in empirical composition by. CHj. Worenine is, therefore, represented by (XXX), the alternative position (a) for the methyl group being untenable, since a-methyltetra-hydrocoptisine obtained by Freund s method is not identical with... 

Curare was first examined by Roulin and Boussingalt, who isolated a syrupy body, which they named curarine much later a similar substance was obtained by Buchner, - and in 1865 Preyer announced that he had obtained curarine and its salts in a well-crystallised condition, and by analysis of the platinichloride, ascertained its composition to be C10H35N. Sachs - was only able to obtain an amorphous alkaloid, to which he assigned the formula CigHjjN. The work of Boehm explained to some extent these discrepant results he examined all three varieties and showed that they differed in composition, and that the isolation of the various curarines as single substances required special processes. 

Amorphous alloys are in a thermodynamically metastable state, and hence essentially they are chemically more reactive than corresponding thermodynamically stable crystalline alloyIf an amorphous alloy crystallises to a single phase having the same composition as the amorphous phase, crystallisation results in a decrease in the activity of the alloy related to the active dissolution rate of the alloy . 

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