formaldehyde - Sciencemadness Dot Org
formaldehyde - Sciencemadness Dot Org
formaldehyde - Sciencemadness Dot Org
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USES OF FORMALDEHYDE 321<br />
scopic, or syrupy materials which, are claimed to hinder the deposition 01<br />
<strong>formaldehyde</strong> polymer on the seeds and thus prevent damage and increase<br />
the disinfecting action 4 .<br />
References<br />
1. Anderson, P- J-, Conn. Agr. Expt. Sta., Bull, 359,336-64 • 1934 : C\ A.. 2S„ 0&2Q.<br />
2. Brauxi, Hh, J. Agr. Research, 19, 363-95 (1920)j Chem. Zerdr.t 1921, II, :«7.<br />
3. Cbemische Fabrik Ludwig Meyer, French Patent o65,l&S \lfl24;-.<br />
4. Chemiscne Fabrik Ludwig Meyer, German Patent 423,466 (1926;; Chem. Ztntr., 1906,0, 4S3.<br />
5. Cook, H. T., and Nugent, T. J., Virginia, Truck Expi. Sta, Bull. 104.13(3-1717 1940;.<br />
6. Dairies, R. H., New Jersey Agr. Expt* Sta., Circular Xo. 437, Spp, '1942 .<br />
7. Garman, P., Afr. Expt. Sta., Conn. Sept., 48.305-7; CAwa. Zentr., 1926, U\ 1175.<br />
S. Hurd, A, M„ J. .40r. R&tearch, 20, 209-41 (1920); C. .4., 15, 69S.<br />
S. JIoU, E., (to Chemiscbe Fabrik Ludwig Meyer), t". S. Paienr 1.530,950 1925'!.<br />
10. Morris, R. H., T7. S. Patent 1,394,482 (192S).<br />
11. Neill, •?• C, NetvZetzland J. Agr., 31, 24-5 (1925); C. A., 30, 472,<br />
1?. Ogilvie, L., Hickman, C. J., and Croxail, H. E., Ana. Rept. Agr. Hon. Research Sta., Long Asbion* Bristol<br />
1938, 9S-114;C. .4.,34,1121.<br />
13. Reyneke, J., Farming in 3. Africa, Ut &4r-B (13391; J". $oc. Cfem, fnd,, 58.3171.<br />
XL Sayre, J. D., and Thomas, R, C. Science, 66, 39S '1927}; C. .4., 22, 299.<br />
15, Sayre, J. D., and Thomas, &. C.; Ohio Agr. Expt. Sta., Bimonthly Bull., 13,19-21 ri82S>; C. A., 23,1011.<br />
15. Stewart, R., and Stephens, J., Utah Expt. Sta. Bull. 108, (2910'; C. A., 4, 2972.<br />
17 Traverso, G. B-, Stat, sperim. agrariitaL, 52T 463-54 f 1919*1; Clem, Zentr., 192*, I, 92S.<br />
Formaldehyde as a Reagent for Chemical Analyses<br />
Small quantities of foi*maldehyde are employed for a variety of purposes<br />
in quantitative and qualitative analyses. Although for some of these<br />
purposes it has been replaced by other reagents, it remains a key chemical<br />
in several well known analytical procedures commonly employed in modern<br />
technical laboratories.<br />
The Sorenson procedure for the titration of amino acids is perhaps the<br />
best known, of the analytical procedures in which <strong>formaldehyde</strong> is employed.<br />
Reaction with <strong>formaldehyde</strong> makes it possible to carry out direct<br />
titration of these acids, since the basic properties of the amino radicals are<br />
nullified by <strong>formaldehyde</strong> condensation. The reactions upon which this<br />
procedure is based have been already discussed (page 220).<br />
Formaldehyde is also commonly employed for the quantitative determination<br />
of halogen acids or inorganic halides in the presence of hydrocyanic<br />
acid or alkali cyanides. The solution to be analyzed is made alkaline with<br />
caustic and treated with excess <strong>formaldehyde</strong>. By this means cyanides are<br />
converted to <strong>formaldehyde</strong> eyanohydrin which will not interfere in the<br />
volumetric determination of halogen by the Yolhard procedure, which can<br />
be applied after the solution has been acidified with nitric acid. This<br />
procedure was described by Polstorf and Meyer 6 in 1912. A recent paper<br />
by Mutschin 7 gives detailed directions for determining chlorides, bromides<br />
and iodides in the presence of CX~ with Mohr's method of titration following<br />
the addition of <strong>formaldehyde</strong>.<br />
Precipitation of metals by the addition of <strong>formaldehyde</strong> and alkali to<br />
solutions containing salts or oxides of gold 10 , silver 11 , bismuth 2 -" and copper 5