Chlorination Sentence Examples

As calciners they are used in tin mines and for the chlorination of silver ores.

Long-continued treatment with halogens may, in some cases, result in the formation of aromatic compounds; thus perchlorbenzene, C 6 C1 6, frequently appears as a product of exhaustive chlorination, while hexyl iodide, C 6 H 13 I, yields perchlorand perbrom-benzene quite readily.

Simple chlorination units using sodium hypochlorite (bleach) help to ensure potability to point of use.

Chlorination of this substance gave a monochloracetic acid; we will assume the chlorine atom to replace the b hydrogen atom.

Chlorination of water may account for a small rise in cancer risk.

When treated with chlorine, pyrocatechol (1.2 or ortho-dioxybenzene) (1) yields a tetrachlor ortho-quinone, which suffers further chlorination to hexachlor-o-diketo-R-hexene (2).

Chlorination in the cold gives orthoand para-chlortoluenes, but at the boiling point the side chain is substituted (see Benzaldehyde).

The ultimate chlorination product of copper, CuC1 2, when heated to redness, decomposes into the lower chloride, CuCI, and chlorine.

Both fixed and rotating vats are employed, the chlorination proceeding more rapidly in the latter case; rotating barrels are sometimes used.

After charging, the barrel is rotated, and when the chlorination is complete the contents are emptied on a filter of quartz or some similar material, and the filtrate led to settling tanks.

Effective avoidance of chlorination byproducts could therefore require major changes in behavior.

Sterilization of instruments and solutions used in the eye can help prevent the spread of EKC, as can adequate chlorination of swimming pools.

This compound is readily oxidized to benzoic acid, C 6 H 5 000H, the aromatic residue being unattacked; nitric and sulphuric acids produce nitro-toluenes, C6H4 CH3 N02j and toluene sulphonic acids, C 6 H 4 CH 3 SO 3 H; chlorination may result in the formation of derivatives substituted either in the aromatic nucleus or in the side chain; the former substitution occurs most readily, chlor-toluenes, C 6 H 4 CH 3 Cl, being formed, while the latter, which needs an elevation in temperature or other auxiliary, yields benzyl chloride, C 6 H 5 CH 2 C1, and benzal chloride, C 6 11 5 CHC1 2.