Toxicity phenol hydrogenation

The experimental first-order decay rate for pentachlorobenzene in an aqueous solution containing a nonionic surfactant micelle (Brij 58, a polyoxyethylene cetyl ether) and illuminated by a photoreactor equipped with 253.7-nm monochromatic UV lamp is 1.47 x lO Vsec. The corresponding half-life is 47 sec. Photoproducts reported include all tetra-, tri-, and dichlorobenzenes, chlorobenzene, benzene, phenol, hydrogen, and chloride ions (Chu and Jafvert, 1994). Chemical/Physical. Emits toxic chlorinated acids and phosphene when incinerated (Sittig,... 

Many allelochemicals are decomposed in soil, either abiotically (37) or by microorganisms (95-100). Obviously, the attainment of active concentrations of allelochemicals in soil depends on the relative rates of addition and inactivation. It is important to understand also that microbial decomposition of allelochemicals does not necessarily result in a decrease in allelopathic activity. In fact, the reverse may be true. Hydrojuglone is oxidized in soil to juglone, a quinone that is inhibitory to some species at a 10 ° M concentration (101). Isoflavonoids produced by red clover are decomposed to even more toxic phenolic compounds (95) and to repeat, amygdalin from peach roots is changed to hydrogen cyanide and benzaldehyde which cause the peach replant problem (88), and phlorizin from apple roots is decomposed to several phenolic compounds that appear to be responsible for the apple replant problem (100). 

CAUTION Toxicity) Phenols, formaldehyde, and other aldehydes are toxic and should be handled with adequate ventilation and skin protection [17]. Where possible the use of hydrogen chloride in the presence of formaldehyde or formaldehyde sources (hexamethylenetetramine and the like) should be avoided. Recent reports have indicated that formaldehyde and hydrogen chloride spontaneously react to give the known carcinogen 6w(chloromethyl) ether. 

Wet peroxide oxidation processes using hydrogen peroxide as oxidant have emerged as a viable alternative for the hquid phase oxidation of phenol. Hydrogen peroxide does not form any harmful by-products, and it is a non-toxic and ecological reactant [6]. 

Toxic or malodorous pollutants can be removed from industrial gas streams by reaction with hydrogen peroxide (174,175). Many Hquid-phase methods have been patented for the removal of NO gases (138,142,174,176—178), sulfur dioxide, reduced sulfur compounds, amines (154,171,172), and phenols (169). Other effluent treatments include the reduction of biological oxygen demand (BOD) and COD, color, odor (142,179,180), and chlorine concentration. 

Toxic Reactions of the Skin Irritation is the most common reaction of the skin. Skin irritation is usually a local inflammatory reaction. The most common skin irritants are solvents dehydrating, oxidizing, or reducing compounds and cosmetic compounds. Acids and alkalies are common irritants. Irritation reactions can be divided into acute irritation and corrosion. Necrosis of the surface of the skin is typical for corrosion. Acids and alkalies also cause chemical burns. Phenols, organotin compounds, hydrogen fluoride, and yellow phosphorus may cause serious burns. Phenol also causes local anesthesia, in fact it has been used as a local anesthetic in minor ear operations such as puncture of the tympanous membrane in cases of otitis. ... 

Phenolic compounds take part in protection, regeneration and degradation processes caused by toxic pollutants [81]. An increase in the phenolic level is commonly observed after exposure to hydrogen fluoride [82], sulphur dioxide [83] and especially to ozone [84]. 

Reductive dehalogenation of chlorinated phenols to phenol, cyclohexanol and other chlorine-free compounds takes place rapidly with hydrogen gas and Pd/C in an aqueous system or under solvent-free conditions. Thus, pentachloro phenol was able to be completely dechlorinated within 20 min (Scheme 4.45). This methodology enables a facile route for rapid and complete detoxification of highly toxic polychlorinated aromatic hydrocarbons and environmental remediation71,72. 

Aromatic amines and some other compounds are also effective hydrogen transfer agents and will give excellent molecular stability in most cases when used in place of the hindered phenolics. However, these compounds are rapidly oxidized to form color bodies in the polymer and may be toxic compared with the phenolics. Hence, aromatic amines are not widely used in polypropylene stabilizer systems. 

Chlorinated Hydrocarbons Other Chlorinated Compounds. The substitution of chlorine atom for hydrogen in a compd greatly increases the anesthetic action of the derivative. In addn, the chlorine deriv is less specific than the parent hydrocarbon in its action, and may affect other tissues along with those of the central nervous system of this body. The chlorine deriv is generally quite toxic and may cause liver, heart Sc kidney damage. As a rule, unsaturated chlorine derivs are highly narcotic but less toxic than saturated derivs. Sax(Ref 4) has discussed in detail the toxicities Sc hazards of a number of chlorinated compds, including Chlorinated Diphenyls Chlorinated Hydrocarbons, Aromatic Aliphatic Chlorinated Naphthalenes Chlorinated Phenols Chlorinated Triphenyls others. 

---