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Corrosion methanol

HOCH2C = CCH2OH. White solid, m.p. 58 C, b.p. 238- C prepared by the high pressure reaction between ethyne and methanol and also from BrMgCCMgBr and methanal. Used in electroplating (Ni), as a corrosion inhibitor, and in paint and varnish removal. [Pg.73]

Organic fluids also are mixed with water to serve as secondary coolants. The most commonly used fluid is ethylene glycol. Others include propjiene glycol, methanol (qv), ethanol, glycerol (qv), and 2-propanol (see Propyl alcohols, isopropyl alcohol). These solutions must also be inhibited against corrosion. Some of these, particularly methanol, may form flammable vapor concentrations at high temperatures. [Pg.509]

Ion implantation has also been used for the creation of novel catalyticaHy active materials. Ruthenium oxide is used as an electrode for chlorine production because of its superior corrosion resistance. Platinum was implanted in mthenium oxide and the performance of the catalyst tested with respect to the oxidation of formic acid and methanol (fuel ceU reactions) (131). The implantation of platinum produced of which a catalyticaHy active electrode, the performance of which is superior to both pure and smooth platinum. It also has good long-term stabiHty. The most interesting finding, however, is the complete inactivity of the electrode for the methanol oxidation. [Pg.398]

Organic compounds normally cause Htde or no corrosion of magnesium. Tanks or other containers of magnesium alloys are used for phenol [108-95-2] methyl bromide [74-96 ] and phenylethyl alcohol [60-12-8]. Most alcohols cause no more than mild attack, but anhydrous methanol attacks magnesium vigorously with the formation of magnesium methoxide [109-88-6]. This attack is inhibited by the addition of 1% ammonium sulfide [12135-76-1] or the presence ofwater. [Pg.334]

In petroleum and oxygenate finish removers, the major ingredient is normally acetone, methyl ethyl ketone [78-93-3], or toluene. Cosolvents include methanol, / -butanol [71-36-3], j -butyl alcohol [78-92-2], or xylene [1330-20-7]. Sodium hydroxide or amines are used to activate the remover. Paraffin wax is used as an evaporation retarder though its effectiveness is limited because it is highly soluble in the petroleum solvents. CeUulose thickeners are sometimes added to liquid formulas to assist in pulling the paraffin wax from the liquid to form a vapor barrier or to make a thick formula. Corrosion inhibitors are added to stabili2e tbe formula for packaging (qv). [Pg.551]

Polytitanosiloxane (PTS) polymers containing Si—O—Ti linkages have also been synthesized through hydrolysis—polycondensation or hydrolysis—polycondensation—pyrolysis reactions involving clear precursor sol solutions consisting of monomeric silanes, TYZOR TET, methanol, water, and hydrochloric acid (Fig. 2). These PTS polymers could be used to form excellent corrosion protection coatings on aluminum substrates (171). [Pg.152]

Polymer-supported catalysts incorporating organometaUic complexes also behave in much the same way as their soluble analogues (28). Extensive research has been done in attempts to develop supported rhodium complex catalysts for olefin hydroformylation and methanol carbonylation, but the effort has not been commercially successful. The difficulty is that the polymer-supported catalysts are not sufftciendy stable the valuable metal is continuously leached into the product stream (28). Consequendy, the soHd catalysts fail to eliminate the problems of corrosion and catalyst recovery and recycle that are characteristic of solution catalysis. [Pg.175]

Chromates are used to inhibit metal corrosion in recirculating water systems. When methanol was extensively used as an antifree2e, chromates could be successfully used as a corrosion inhibitor for cooling systems in locomotive diesels and automobiles (185). [Pg.143]

Ethanol water is a solution of denatured grain alcohol. Its main advantage is that it is nontoxic and thus is widely used in the food and chemic industry. By using corrosion inhibitors it could be made non-corrosive for brine service. It is more expensive than methanol water and has somewhat lower heat transfer coefficients. As an alcohol derivate it is flammable. [Pg.1125]

To meet sales specifications, gas produced at the wellheads must be free of water and hydrocarbon liquids. Twin turboexpanders are a key component in this process, providing dewpoint control with optimal efficiency. Initial processing takes place at the wellhead platforms, where methanol is injected to inhibit hydrate formation. A corrosion inhibitor is also added to prevent gas from damaging downstream equipment. [Pg.451]

In hydrochloric acid at temperatures up to 100°C, the corrosion rate decreases with time and ferric iron concentration . The presence of air does not affect the general corrosion rate but in IOn acid it promotes pitting attack, which also arises in chloride-containing methanolic solutions in the absence of sufficient water to effect passivation . Alloying niobium with 2.5% or more of tantalum significantly decreases corrosion rates in hydrochloric acid . [Pg.860]

For commercially pure titanium, the specific environments to be avoided are pure methanol and red, fuming nitric acid " , although in both environments the presence of 2% of water will inhibit cracking. On the other hand, the presence of either bromine or iodine in methanol aggravates the effect. When it does occur, stress-corrosion cracking of commercially pure titanium is usually intergranular in habit. [Pg.873]

The stress-corrosion cracking hazard for titanium alloys containing aluminium is significantly higher than that obtaining for commercially pure titanium, and in addition to stress-corrosion cracking in methanol and red... [Pg.879]

Intergranular corrosion Carbon steels in NO solns Some Al alloys in Cl Cu-Zn alloys solns, high in NH7 solns potentials Fe-Cr-Ni steels in Cl solns Cu-Zn alloys Mg-A alloys in NO in CrO + solns Cl solns Ti alloys in High methanol. A strength alloys, low steels in Cl potentials solns Brittle fracture... [Pg.1173]

The two principal forms of stress-corrosion failure are (a) hot salt cracking and (Z)) room-temperature cracking, the latter occurring in both aqueous and methanolic chloride environments, and in N2O4. In addition, environmental failures can occur in alloys in direct contact with some liquid and solid metals, and certain gases. [Pg.1259]

Many titanium alloys are susceptible to stress-corrosion cracking in aqueous and methanolic chloride environments. [Pg.1262]


See other pages where Corrosion methanol is mentioned: [Pg.446]    [Pg.83]    [Pg.200]    [Pg.112]    [Pg.608]    [Pg.446]    [Pg.83]    [Pg.200]    [Pg.112]    [Pg.608]    [Pg.67]    [Pg.425]    [Pg.425]    [Pg.433]    [Pg.503]    [Pg.508]    [Pg.87]    [Pg.185]    [Pg.195]    [Pg.195]    [Pg.278]    [Pg.200]    [Pg.190]    [Pg.186]    [Pg.1125]    [Pg.1147]    [Pg.556]    [Pg.794]    [Pg.796]    [Pg.308]    [Pg.149]    [Pg.138]    [Pg.197]    [Pg.455]    [Pg.868]    [Pg.1161]    [Pg.1265]    [Pg.1265]    [Pg.1310]    [Pg.80]   
See also in sourсe #XX -- [ Pg.265 ]




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