Acidic materials

The following cautions should be observed Do not destroy or remove inhibitor. Do not contaminate with alkaline or strongly acidic materials. Do not store in the presence of a water layer. In the event of spillage or misuse that cause a release of product vapor to the atmosphere, thoroughly ventilate the area, especially near floor levels where vapors will collect. 

Tannins occur in many plants and are separated by extraction. At present, only quebracho extract is used as a mud thinner in significant quantity in the United States. Quebracho is an acidic material and performs best at high pH. It is an excellent thinner for lime-treated and cement-contaminated muds. However, it is not effective at high salt concentrations. Sulfomethylated tannin products are functional over a wide range of pH and salinity and have either been treated with chromium for good thermal stabiUty (58) or are chrome free. Concentrations of tannin additives are ca 1.5—18 kg/m (0.5—6 lb/bbl). 

Retarders were originally arenecarboxylic acids. These acidic materials not only delay the onset of cross-linking but also slow the cross-linking reaction itself. The acidic retarders do not function weU in black-fiUed compounds because of the high pH of furnace blacks. Another type of retarder, A/-nitroso diphenylamine [86-30-6] was used for many years in black-fiUed compounds. This product disappeared when it was recognized that it trans-nitrosated volatile amines to give a several-fold increase in airborne nitrosamines. U.S. production peaked in 1974 at about 1.6 million kg. 

Other ingredients besides the elastomer and the cure system itself influence cure and scorch behavior. Usually the effect of a material on cure is pH-dependent. Ingredients which are basic in nature tend to accelerate the rate of both scorch and cure, whereas acidic materials exhibit the opposite effect. 

Some of the more obvious sources of contamination of solvents arise from storage in metal drums and plastic containers, and from contact with grease and screw caps. Many solvents contain water. Others have traces of acidic materials such as hydrochloric acid in chloroform. In both cases this leads to corrosion of the drum and contamination of the solvent by traces of metal ions, especially Fe. Grease, for example on stopcocks of separating funnels and other apparatus, e.g. greased ground joints, is also likely to contaminate solvents during extractions and chemical manipulation. 

Charcoal is generally satisfactorily activated by heating gently to red heat in a crucible or quartz beaker in a muffle furnace, finally allowing to cool under an inert atmosphere in a desiccator. Good commercial activated charcoal is made from wood, e.g. Norit (from Birch wood), Darco and Nuchar. If the cost is important then the cheaper animal charcoal (bone charcoal) can be used. However, this charcoal contains calcium phosphate and other calcium salts and cannot be used with acidic materials. In this case the charcoal is boiled with dilute hydrochloric acid (1 1 by volume) for 2-3h, diluted with distilled water and filtered through a fine grade paper on a Buchner flask, washed with distilled water until the filtrate is almost neutral, and dried first in air then in a vacuum, and activated as above. To improve the porosity, charcoal columns are usually prepared in admixture with diatomaceous earth. 

The most common impurities are the corresponding acid and hydroxy compound (i.e. alcohol or phenol), and water. A liquid ester from a carboxylic acid is washed with 2N sodium carbonate or sodium hydroxide to remove acid material, then shaken with calcium chloride to remove ethyl or methyl alcohols (if it is a methyl or ethyl ester). It is dried with potassium carbonate or magnesium sulfate, and distilled. Fractional distillation then removes residual traces of hydroxy compounds. This method does not apply to esters of inorganic acids (e.g. dimethyl sulfate) which are more readily hydrolysed in aqueous solution when heat is generated in the neutralisation of the excess acid. In such cases, several fractional distillations, preferably under vacuum, are usually sufficient. 

Because phenols are weak acids, they can be freed from neutral impurities by dissolution in aqueous N sodium hydroxide and extraction with a solvent such as diethyl ether, or by steam distillation to remove the non-acidic material. The phenol is recovered by acidification of the aqueous phase with 2N sulfuric acid, and either extracted with ether or steam distilled. In the second case the phenol is extracted from the steam distillate after saturating it with sodium chloride (salting out). A solvent is necessary when large quantities of liquid phenols are purified. The phenol is fractionated by distillation under reduced pressure, preferably in an atmosphere of nitrogen to minimise oxidation. Solid phenols can be crystallised from toluene, petroleum ether or a mixture of these solvents, and can be sublimed under vacuum. Purification can also be effected by fractional crystallisation or zone refining. For further purification of phenols via their acetyl or benzoyl derivatives (vide supra). 

Diethyl sulfate [64-67-5] M 154.2, b 96 /15mm, 118 /40mm, d 1.177, n 1.399. Washed with aqueous 3% Na2C03 (to remove acidic material), then distilled water, dried (CaCl2), filtered and distd. Causes blisters to the skin. 

Dihydroxybenzoic acid [303-07- ] M 154.1, m 167"(dec), pK 1.05. Dissolved in aqueous NaHC03 and the soln was washed with ether to remove non-acidic material. The acid was ppted by adding H2SO4, and recrystd from water. Dried under vacuum and stored in the dark [Lowe and Smith J Chem Soc, Faraday Trans I 69 1934 1973],... 

The acetal polymers are probably never supplied for use without any additives being incorporated. As mentioned in Section 19.3.1 antioxidants of the phenol alkane type are present in both homopolymers and copolymers. Acid acceptors are also believed to be widely used to absorb traces of acidic materials which attack the acetal linkage. Epoxides, nitrogen compounds and basic salts have been successfully employed. 

Table 21.8 Some properties of compression moulded polyfparabanic acid) materials at 23°C22...

Chemical Reactivity - Reactivity with Water No reaction Reactivity with Common Materials Contact with any acidic material will form poisonous hydrogen cyanide gas, which may collect in enclosed spaces Stability During Transport Stable Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Not pertinent Inhibitor cf Polymerization Not pertinent. 

These problems of engine lubrication can be overcome by using highly refined oil. The resistance to oxidation is further enhanced by the use of anti-oxidants. The addition of corrosion-inhibitors counters acidic materials produced by combustion at low engine temperatures. 

Most organic substances can be dissolved readily in a suitable organic solvent and some are directly soluble in water or can be dissolved in aqueous solutions of acids (basic materials) or of alkalis (acidic materials). Many inorganic substances can be dissolved directly in water or in dilute acids, but materials such as minerals, refractories, and alloys must usually be treated with a variety of reagents in order to discover a suitable solvent in such cases the preliminary qualitative analysis will have revealed the best procedure to adopt. Each case must be considered on its merits no attempt at generalisation will therefore be made. It is however of value to discuss the experimental technique of the simple process of solution of a sample in water or in acids, and also the method of treatment of insoluble substances. 

Naturally, the flux employed will depend upon the nature of the insoluble substance. Thus acidic materials are attacked by basic fluxes (carbonates, hydroxides, metaborates), whilst basic materials are attacked by acidic fluxes (pyroborates, pyrosulphates, and acid fluorides). In some instances an oxidising medium is useful, in which case sodium peroxide or sodium carbonate mixed with sodium peroxide or potassium nitrate may be used. The vessel in which fusion is effected must be carefully chosen platinum crucibles are employed for... 

Another application for polyelectrolyte materials is in the forming plastics with unusual physical properties with regard to adhesion. The incorporation of small amounts of organic acid materials into polyolefin structures results in materials that have excellent adhesion to metals, paper, glass, and a variety... 

Phosphonobutane-l,2,4-tricarboxylic acid (PBTC) is the most expensive of the commonly used phosphonates. However it is excellent at providing calcium carbonate control under highly stressed operating conditions. It is most resistant to the problem of calcium phosphonate precipitation and, from an environmental position, has the lowest phosphorus content of the common phosphonates. The acid material has a MW of 270. PBTC has a sequestration value of 280 mg CaC03/g product at a pH level of 11. It is very stable and can operate under very high pH conditions. However, it may also attack copper. Examples include Bayhibit AM, Mayoquest 2100, Phos -9, and Codex 551. 

Initial hydrolysis would therefore lead to further hydrolysis and pH drop in storage tanks, resulting in a product that is difficult to recover and may cause irreparable damage (corrosion) in tanks, pipelines, and pumps. Therefore the pH must be kept high (9-11) to avoid acid material entering bulk storage (steep titration curve). If for product formulation requirements a product of pH 6-7 is essential, the use of buffers, e.g., phosphoric acid or citric acid, is recommended. 

Acidic materials in the atmosphere (e.g. CO2 and H2CO3, SO2 and H2SO3, HNO3 and so on) coexist with basic materials in both igneous and sedimentary rocks (e.g. FeS2 and CaCOa). 

An important development has been the isolation of bacteria that were able to degrade phenan-threne that was sorbed to humic acid material (Vacca et al 2005). Enrichment was carried ont with PAH-contaminated soils using phenanthrene sorbed to commercial hnmic acid. Only the strains isolated from this enrichment were able to carry ont degradation of C-labeled phenanthrene, and this exceeded by factors of 4-9 the amonnt estimated to be available from the aqneons phase alone. It was snggested that specially adapted bacteria might interact specifically with natnrally occnrring colloidal material. 

If acid-sensitive analytes (e.g., myclobutanil, propiconazole, tebuconazole, fiuotri-mazole, thiabendazole, carbendazim) are extracted from an acidic material (e.g., citrus fruits, berries, several sorts of apples and tomatoes), only low recoveries are obtained. If the pH of an aqueous homogenate of the material is <5, use Module E3, where the acids are neutralized before the extraction. 

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