Similarity aluminium-based

Detailed studies of systems involving aluminium-based Lewis acids and hydrogen halides are scarce. Fontana and Kidder investigated the polymerisation of propene initiated by the pair aluminium bromideTiydrt n bromide. The cocatalytic role of the latter acid was clearly proved since no polymerisation could be detected in its absence. The dependence of the rate of polymerisation upon the cocatalyst concentration and the induction periods observed make this system similar to those in which stannic chloride induces the polymerisation of olefins in the presence of variable quantities of water (see Sect. IV-C-3-b). With relatively large quantities of added hydrogen bromide, addition of this acid to the mcmomer to give fso-propyl bromide must have constituted an important side reaction. 

Phosgene has been employed in the modification of the surfaces of cellulose-acetate membranes used for water desalination and waste water treatment [1450]. Similarly, phosgene has been used to surface-modify porous diaphragms for electrolytic cells [324]. Aluminium and aluminium-based alloys can be etched at a high rate when COClj is used in a mixed gas plasma [1004], as can semiconductors (see Section 9.12). 

RSD of 40-60% at 1 /poor performance. Methodology of itself does not seem to be a key factor, since most laboratories have been using similar methodology based on graphite furnace atomic absorption spectrometry. The most important factor appears to be the experience of the laboratory carrying out the analysis. For some schemes, there has been a dramatic rise in the number of participants, mostly of laboratories with very little previous experience of trace element analysis (Taylor, 1990). With the exception of a number of experienced laboratories, the performance of a large number of laboratories is insufficient to allow a proper assessment of aluminium exposure (Taylor, 1990). The performance of laboratories has also been impeded by the lack of suitable reference materials, particularly in the case of water and dialysis fluid. 

A similar catalytic dimerization system has been investigated [40] in a continuous flow loop reactor in order to study the stability of the ionic liquid solution. The catalyst used is the organometallic nickel(II) complex (Hcod)Ni(hfacac) (Hcod = cyclooct-4-ene-l-yl and hfacac = l,l,l,5,5,5-hexafluoro-2,4-pentanedionato-0,0 ), and the ionic liquid is an acidic chloroaluminate based on the acidic mixture of 1-butyl-4-methylpyridinium chloride and aluminium chloride. No alkylaluminium is added, but an organic Lewis base is added to buffer the acidity of the medium. The ionic catalyst solution is introduced into the reactor loop at the beginning of the reaction and the loop is filled with the reactants (total volume 160 mL). The feed enters continuously into the loop and the products are continuously separated in a settler. The overall activity is 18,000 (TON). The selectivity to dimers is in the 98 % range and the selectivity to linear octenes is 52 %. 

The data given in Tables 1.9 and 1.10 have been based on the assumption that metal cations are the sole species formed, but at higher pH values oxides, hydrated oxides or hydroxides may be formed, and the relevant half reactions will be of the form shown in equations 2(a) and 2(b) (Table 1.7). In these circumstances the a + will be governed by the solubility product of the solid compound and the pH of the solution. At higher pH values the solid compound may become unstable with respect to metal anions (equations 3(a) and 3(b), Table 1.7), and metals like aluminium, zinc, tin and lead, which form amphoteric oxides, corrode in alkaline solutions. It is evident, therefore, that the equilibrium between a metal and an aqueous solution is far more complex than that illustrated in Tables 1.9 and 1.10. Nevertheless, as will be discussed subsequently, a similar thermodynamic approach is possible. 

Aluminium anodes comprise essentially three generic types Al-Zn-In, Al-Zn-Hg and Al-Zn-Sn. Since Al-Zn-Sn alloys have largely been superseded, they will not be discussed further. Indium and mercury are added to aluminium to act as activators, i.e. to overcome the natural passivation of aluminium. Despite this, aluminium anodes are not suitable for low chloride environments which would lead to passivation. These anodes are therefore not used for land-based applications (although examples of use in environments such as swamps do exist). Similarly their use in low chloride aqueous environments such as estuaries must be viewed with caution. 

Laister and Benham have shown that under more arduous conditions (immersion for 6 months in sea-water) a minimum thickness of 0-025 mm of silver is required to protect steel, even when the silver is itself further protected by a thin rhodium coating. In similar circumstances brass was completely protected by 0 012 5 mm of silver. The use of an undercoating deposit of intermediate electrode potential is generally desirable when precious metal coatings are applied to more reactive base metals, e.g. steel, zinc alloys and aluminium, since otherwise corrosion at discontinuities in the coating will be accelerated by the high e.m.f. of the couple formed between the coating and the basis metal. The thickness of undercoat may have to be increased substantially above the values indicated if the basis metal is affected by special defects such as porosity. 

Discussion. This method is based upon the precipitation of lead chlorofluoride, in which the chlorine is determined by Volhard s method, and from this result the fluorine content can be calculated. The advantages of the method are, the precipitate is granular, settles readily, and is easily filtered the factor for conversion to fluorine is low the procedure is carried out at pH 3.6-5.6, so that substances which might be co-predpitated, such as phosphates, sulphates, chromates, and carbonates, do not interfere. Aluminium must be entirely absent, since even very small quantities cause low results a similar effect is produced by boron ( >0.05 g), ammonium (>0.5 g), and sodium or potassium ( > 10g) in the presence of about 0.1 g of fluoride. Iron must be removed, but zinc is without effect. Silica does not vitiate the method, but causes difficulties in filtration. 

Enichem made one of the most important steps forward in the development of general heterogeneous oxidation catalysts in the early 1990s with the commercialization of titanium silicate (TS-1) catalysts. TS-1 has a structure similar to ZSM-5 in which the aluminium has been replaced by titanium it is prepared by reaction of tetraethylorthosilicate and tetra-ethylorthotitanate in the presence of an organic base such as tetrapropy-lammonium hydroxide. This catalyst is especially useful for oxidation reactions using hydrogen peroxide (Scheme 4.11), from which the only byproduct is water, clean production of hydroquinone being one of the possibilities. 

Another feature of meteorites that proves to be important is the calcium-aluminium inclusions (CAIs), which, as the name suggests, show regions of enhanced Ca and Al. These micron- to centimetre-sized particles are some of the oldest objects known and have a similar temperature history. They probably formed at temperatures in the region 1700-2400 K and so are close to the centre line of the solar nebula. Although it is hard to be sure about the origin of these objects, there is agreement on their age based on radioisotope dating. 

Commercial alloys composition, nomenclature. A simple and general way of identification of a commercial alloy (or of a group of similar alloys) consists of a label which gives (as rounded values) the mass% contents of the main components indicated by their chemical symbols. The alloy, for instance, Ti-6A1-4V, is a titanium-based alloy typically containing 6 mass% aluminium and 4 mass% vanadium. 

Complete control of the diastereoselectivity of the synthesis of 1,3-diols has been achieved by reagent selection in a one-pot tandem aldol-reduction sequence (see Scheme l). i Anti-selective method (a) employs titanium(IV) chloride at 5°C, followed by Ti(OPr )4, whereas method (b), using the tetrachloride with a base at -78 °C followed by lithium aluminium hydride, reverses the selectivity. A non-polar solvent is required (e.g. toluene or dichloromethane, not diethyl ether or THF), and at the lower temperature the titanium alkoxide cannot bring about the reduction of the aldol. Tertiary alkoxides also fail, indicating a similarity with the mechanism of Meerwein-Ponndorf reduction. 

---