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Preparation temperature

Stannous oxalate is used as an esterification and transesterification catalyst for the preparation of alkyds, esters, and polyesters (172,173). In esterification reactions, it limits the undeskable side reactions responsible for the degradation of esters at preparation temperatures. The U.S. Bureau of Mines conducted research on the use of stannous oxalate as a catalyst in the hydrogenation of coal (174) (see Coal). [Pg.75]

Al Ti in the range of 0.9—1.0 appeared optimum for i7j -l,4-polyisoprene yield (20). Other factors such as catalyst preparation temperature, influence of the R group in the alkyl aluminum compound (R Al), and catalyst aging have been extensively studied (16,17). Another variable studied was the effect of... [Pg.4]

It should be noted that the properties of a CTC depend to a considerable degree on the conditions of their preparation. Temperature increase, in particular, favors the accumulation of complete charge transfer states in a CTC. In the case of a CTC obtained in solution, the increase of dielectric constant of the solvent has the same effect. The method of preparation of a CTC also affects the kinetic curves of the accumulation and depletion of complete transfer states arising at protoirradiation. [Pg.33]

Compound Preparation" Temperature (°C) Time (days) Temperature of decomposition (°C) (g/cm ) Ref... [Pg.385]

Fig. 2. Average anatase crystallite sizes and fractions of rutile phase as a function of preparation temperature in conventional spray pyrolysis. Fig. 2. Average anatase crystallite sizes and fractions of rutile phase as a function of preparation temperature in conventional spray pyrolysis.
Another distinguishing feature of titania prepared by flame spray pyrolysis is the draar e of anatase crystallite size with the increase of flame temperature. Generally, the increase of preparation temperature increases the crystallite size in other processes such as sol-gel method, hydrothermal method [2, 3], flame processing and conventional spray pyrolysis. The decrease of crystallite size was directly related to the decrease of particle size. Fig. 5 shows SEM and TEM images of titania particles prepared by flame spray pyrolysis. [Pg.763]

Compared with the conventional spray pyrolysis, flame spray pyrolysis produces titania particles that are strikingly different in crystd phase and surfece arra. The fraction of anatase phase increases with the increase of flame tempCTature while it decreases with the increase of preparation temperature in the conventional spray pyrolysis. The sur e area and... [Pg.764]

The practices of isocratic and gradient sorptive chromatography are very different. Isocratic chromatography tends to be very sensitive to the details of mobile phase preparation, temperature, pump speed, and sample composition. Gradient chromatography is usually more tolerant of small variations in these factors but may be extremely sensitive to column history, equilibration time, and gradient preparation. [Pg.22]

The authors conducted a similar investigation of precatalysts 7 and 11 using TiBA and trityl tetrakis(pentafluorophenyl)borate as the cocatalyst. They concluded that this material contained no fraction that could be characterized as blocky. It was therefore proposed that reversible chain transfer occurred only with MAO or TMA and not with TiBA. This stands in contrast to the work of Chien et al. [20] and Przybyla and Fink [22] (vida supra), who claim reversible chain transfer with TiBA in similar catalyst systems. Lieber and Brintzinger also investigated a mixture of isospecific 11 and syndiospecific 12 in attempts to prepare iPP/sPP block copolymers. Extraction of such similar polymers was acknowledged to be difficult and even preparative temperature rising elution fractionation (TREF) [26, 27] was only partially successful. [Pg.73]

Factors influencing the acid properties of zeolites include the method of preparation, temperature of dehydration, the silica to alnmina ratio, and the distribntion of the framework atoms [106-108]. [Pg.209]

R. Iwamoto, S. Hidaka, I. Nakamura and A. lino Effect of preparation temperature... [Pg.162]

Three Fe supported zeolites were prepared by modifying NH Y with 0.25M Fe(N03)3 at various temperatures from 293K to 373K, Figure 2 shows the influence of preparation temperature on physicochemical properties and catalytic activity of the obtained catalysts. [Pg.162]

Fig. 2 Correlation between preparation temperature and physicochemical properties as well as catalytic properties of the Fe supported zeolite. Fig. 2 Correlation between preparation temperature and physicochemical properties as well as catalytic properties of the Fe supported zeolite.
Control of the pH and temperature of the precipitating solution is important to provide optimised conditions for stoichiometric, homogeneous, fluorhydroxyapatite formation. Similar conditions and set-up can be used for the synthesis of fluoride-substituted apatite crystals with varying size, crystallinity and morphology depending on the preparation temperature [124] a purge of the synthesis system with nitrogen gas ensures the preparation of carbonate-free fluorhydroxyapatite at ambient temperature [125]. [Pg.308]

Other modifications to the reaction conditions of the Brust-Schiffrin method, such as a reduction temperature of — 78 °C and the use of a hyperexcess of hexanethiol, results in an Au38(thiolate)24, based on observations, LDI-TOF mass spectrometry, TGA analysis and elemental analysis [69]. The influence of preparation temperature on the size and monodispersity of dodecylthiol monolayer protected gold clusters has also been reported. Both and SAXS measurements show that higher temperatures increase polydispersity. This modification of poly-dispersity may be related to the existence of a dynamic exchange of thiols at the particle surface with thiols in the solvent [70]. [Pg.145]

Primary alkyl isocyanides are known not to comply simply to homopolymerization. It was recently reported that polyisocyanides prepared with nickel(II) compounds varied in color from yellow to black (22,23). The latter occurred at preparative temperatures in excess of 25° C, or when polymer non-solvents or acids were used. Further, the addition of acids to solutions or suspensions of the yellow polymers also led to black compounds. The NMR spectrum of a soluble polymer sample (i.e. MVPO = 1100) of black poly(ethyl isocyanide) shows methylene resonance shifts to values as occur in nitriles, which were interpreted as giving evidence of rearrangement to a polycyanide... [Pg.125]

Figure 13.2 SEM micrographs of M0O3 and of Mo2N-C corresponding powders platelet size in function of the Mo03 preparation temperature (x 120). Figure 13.2 SEM micrographs of M0O3 and of Mo2N-C corresponding powders platelet size in function of the Mo03 preparation temperature (x 120).
An analysis of the extensive literature data and the data of the authors of this book [1640, 1642, 1655] permits a conclusion that the variations in the physicochemical characteristics of Al(OR)3 are caused by the existence of different types of aggregates and the possibility oftheir mutual transformations. The molecular composition depends on the conditions in the course of sample preparation — temperature, nature ofthe solvent applied, and the age ofthe sample. An important role is also played by the presence in the samples of microamounts of oxocomplexes, which are always formed on sublimation, distillation, and any other thermal treatments. [Pg.227]

These questions lead on to further fundamental questions concerning the shapes and properties of small metal particles. For example, what is the stable shape for a small metal particle How is this affected by size, method of preparation, temperature, gaseous environment, precursor compound, support morphology, etc. Do small metal particles have different electronic properties from bulk metal Do surface electronic properties depend on particle size, and if so, do they vary in the same way as bulk electronic properties When, indeed, is a particle small enough to have unusual properties ... [Pg.150]

The cation conductivity is very small which on one hand leads to the high preparation temperatures but on the other to the favorable defect chemical stability as well as to negligible kinetic de-mixing under fuel cell performance.94... [Pg.46]

The endo-nadimide isomer is obtained if the preparation temperature does not exceed 160 °C. The use of higher temperatures generally induces the partial isomerization of the endo-isomer to the exo one the product obtained in this case is a mixture of both isomers. [Pg.148]


See other pages where Preparation temperature is mentioned: [Pg.148]    [Pg.206]    [Pg.131]    [Pg.762]    [Pg.764]    [Pg.124]    [Pg.117]    [Pg.119]    [Pg.116]    [Pg.280]    [Pg.271]    [Pg.83]    [Pg.261]    [Pg.162]    [Pg.31]    [Pg.85]    [Pg.140]    [Pg.148]    [Pg.269]    [Pg.53]    [Pg.2353]    [Pg.50]    [Pg.199]    [Pg.99]    [Pg.344]    [Pg.206]   
See also in sourсe #XX -- [ Pg.314 ]




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