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Compounds, thermal treatment

Regulations. In order to decrease the amount of anthropogenic release of mercury in the United States, the EPA has limited both use and disposal of mercury. In 1992, the EPA banned land disposal of high mercury content wastes generated from the electrolytic production of chlorine—caustic soda (14), accompanied by a one-year variance owing to a lack of available waste treatment faciUties in the United States. A thermal treatment process meeting EPA standards for these wastes was developed by 1993. The use of mercury and mercury compounds as biocides in agricultural products and paints has also been banned by the EPA. [Pg.108]

The small (10 -lm) coating particles are typically aluminum oxide [1344-28-1/, Al O. These particles can have BET surface areas of 100 to 300 m /g. The thermal and physical properties of alumina crystalline phases vary according to the starting phase (aluminum hydroxide or hydrate) and thermal treatment (see ALUMINUM COMPOUNDS, ALUMINUM OXIDE). [Pg.485]

Silver nitrate (AgN03) is a compound that fulfills the precedent requirements (Till = 212°C), and also it can be easily decomposed into pure silver by thermal treatment at 400 °C. As mentioned before, the basic characterisation technique for this studies is transmission electron microscopy (TEM) the atoms with rather high atomic number would facilitate the detection of the nanorods. [Pg.134]

Organic metal salts retard the development of color in the thermal treatment of PVC, and their ability to react selectively with allylic and tertiary chlorine structures according to Eq. 23 has been demonstrated with model compounds [19,32,113,115]. [Pg.326]

Since hydrofluoride synthesis is based on thermal treatment at relatively high temperatures, the possibility of obtaining certain fluorotantalates can be predicted according to thermal stability of the compounds. In the case of compounds whose crystal structure is made up of an octahedral complex of ions, the most important parameter is the anion-cation ratio. Therefore, it is very important to take in to account the ionic radius of the second cation in relation to the ionic radius of tantalum. Large cations, are not included in the... [Pg.46]

This process occurs at temperatures of about 200-300°C, but in order to complete evaporation of water and homogenization of the product, the temperature of the thermal treatment must be increased, in the final stages of the process, to 400-500°C. Nevertheless, extended thermal treatment or higher temperatures can lead to hydrolysis of the compound according to the following interaction ... [Pg.51]

It is possible, in general, that CoNb2F)2 is present only in the gaseous phase at increased temperatures due to insufficient amounts of ligands that are necessary for the formation of a stable solid compound. Further thermal treatment of Co2Nb03F3 at temperatures of 1000-1100°C leads to the formation of Co4Nb209 crystals with a pseudoilmenite structure. [Pg.54]

Co2Nb03F3 was obtained as a result of the thermal treatment of CoNbOF5, predominantly prepared by the hydrofluoride method [129]. This compound crystallizes in a rutile-type structure that can be achieved due to the statistical distribution of cations within the oxyfluoride octahedrons. [Pg.110]

The main problems encountered in the investigation of tantalum- and niobium-containing fluoride and oxyfluoride complexes are related to the tendency of the compounds to undergo hydrolysis, particularly at elevated/high temperatures. In addition, the interpretations of the observed effects are often nontrivial and unclear due to the relatively complicated inter-particular interactions and changes that occur under thermal treatment. From this point of view, vibration spectroscopy methods are of high importance due to the dependence of solid phase spectra on the temperature, which, above all, stems from the nature of such inter-ionic interactions [369]. [Pg.195]

The phase composition of products obtained from the thermal treatment of LiNbOF4 and NaNbOF4 was investigated using X-ray diffraction and vibration spectroscopy, as reported in [379]. Compounds with the following structures were found M2NbOF5, MNb02F2 and MNbC>3, where M = Li or Na. [Pg.202]

The formation of oxide compounds as a result of the thermal treatment of oxyfluorides is due to high temperature hydrolysis and reduction-oxidation processes. [Pg.216]

An irreversible extinction of the SHG signal at 150-200°C is observed for a number of other fluoride and oxyfluoride compounds of tantalum and niobium that crystallize in centrosymmetric space groups. This phenomenon is especially typical for the compounds prepared by precipitation from solutions [206]. The appearance of the weak SHG signal for such compounds is related to imperfections in their crystal structure and the creation of dipoles. Nevertheless, appropriate thermal treatment improves the structure and leads to the disappearance of dipoles and to the irreversible disappearance of the corresponding SHG signal. [Pg.230]

When thermal treatment is applied under conditions that prevent the hydrolysis of the compounds, partial decomposition takes place at a temperature above 600K. Extended thermal treatment at temperatures above 600K leads to complete decomposition according to the following process [438] ... [Pg.236]

Fluorine appears in hydroxides in the form of ammonium oxyfluoro-metalates, yielding ammonium fluoride upon decomposition during thermal treatment. Ammonium fluoride is not a thermally stable compound and... [Pg.301]

Ammonium hydrofluoride is relatively stable, even in the molten state. In addition to being in contact with tantalum or niobium oxide, the compound will initiate the fluorination process yielding complex tantalum or niobium fluoride compounds. There is no doubt that thermal treatment of the hydroxides at high temperatures and/or at a high temperature rate leads to the enhancement of the defluorination processes, which in turn results in an increase in fluorine content of the final oxides. [Pg.302]

Thermal treatment of the compounds obtained from the hydrolysis leads to their decomposition, yielding tantalum or niobium oxides and gaseous oxygen. The processes of thermal decomposition are given as follows [512] ... [Pg.306]

Table 12. Retentions and yields in organomanganese compounds (not including thermal treatment)... Table 12. Retentions and yields in organomanganese compounds (not including thermal treatment)...
Performance requirements, environmental issues, and avaUabUity/cost of the material will mainly drive material requirement in the future. In order to face the huge tire wastage problem causing major hazards to the environment, future development in mbbery materials will be focused on development of thermoplastic polymer so that used polymer could be recovered by thermal treatment and separation, biological degradation by radiation/addition of chemical into the mbber compound that could be activated by exposure to radiation and development of biopolymer. [Pg.930]

Thermal reactions are the easiest to isolate experimentally, although they are seldom easy to identify precisely. Clearly, any compound whose yield is influenced by thermal treatment involves, in part at least, thermal reactions. These thermal reactions can be of two types those which lead to the addition of further ligands, and those which do not. Only the first type are commonly considered and involve addition of a ligand to complete the molecule to give an identifiable intermediate ... [Pg.238]

The most intensive development of the nanoparticle area concerns the synthesis of metal particles for applications in physics or in micro/nano-electronics generally. Besides the use of physical techniques such as atom evaporation, synthetic techniques based on salt reduction or compound precipitation (oxides, sulfides, selenides, etc.) have been developed, and associated, in general, to a kinetic control of the reaction using high temperatures, slow addition of reactants, or use of micelles as nanoreactors [15-20]. Organometallic compounds have also previously been used as material precursors in high temperature decomposition processes, for example in chemical vapor deposition [21]. Metal carbonyls have been widely used as precursors of metals either in the gas phase (OMCVD for the deposition of films or nanoparticles) or in solution for the synthesis after thermal treatment [22], UV irradiation or sonolysis [23,24] of fine powders or metal nanoparticles. [Pg.234]


See other pages where Compounds, thermal treatment is mentioned: [Pg.282]    [Pg.282]    [Pg.122]    [Pg.509]    [Pg.124]    [Pg.31]    [Pg.54]    [Pg.111]    [Pg.203]    [Pg.204]    [Pg.206]    [Pg.206]    [Pg.206]    [Pg.211]    [Pg.224]    [Pg.227]    [Pg.230]    [Pg.254]    [Pg.304]    [Pg.309]    [Pg.72]    [Pg.75]    [Pg.225]    [Pg.59]    [Pg.103]    [Pg.249]    [Pg.5]    [Pg.103]    [Pg.360]    [Pg.309]    [Pg.574]   
See also in sourсe #XX -- [ Pg.292 ]




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Thermal treatment

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