FREE BOOKS

Author's List




PREV.   NEXT  
|<   425   426   427   428   429   430   431   432   433   434   435   436   437   438   439   440   441   442   443   444   445   446   447   448   449  
450   451   452   453   454   455   456   457   458   459   460   461   462   463   464   465   466   467   468   469   470   471   472   473   474   >>   >|  
wn, with production of "humus," a complex of colloidal "unsaturated" bodies of acid function, they fulfil important chemical functions by interaction with the mineral soil constituents. _Chemistry of Cellulose._--Purified cotton cellulose, which is the definitive prototype of the cellulose group or series, is a complex of monoses or their "residues." It is resolved by solution in sulphuric acid and subsequent hydrolysis of the esters thus produced into dextrose. This fundamental fact with its elementary composition, most simply expressed by the formula C6H10O5, has caused it to be regarded as a polyanhydride of dextrose. Forming, as it does, simple esters in the ratio of the reacting hydroxyls 3OH: C6H10O5, and taking into account its direct converson into [omega]-brom-methyl furfural (Fenton) a constitutional formula has been proposed by A.G. Green (_Zeit. Farb. Textil Chem._ 3, pp. 97 and 309 (1904)), which is a useful generalization of its reactions, and its ultimate relations to the simpler carbohydrates, viz., CH(OH).CH.CH(OH) | >O >O CH(OH).CH.CH2 . Green considers, moreover, that a group thus formulated may consistently represent the actual dimensions of the reacting unit, but that unit of larger dimensions, if postulated, is easily derived from the above by oxygen linkings. From another point of view the unit group has been formulated as /CH(OH).CH(OH) CO >CH2 \CH(OH).CH(OH) , the main linking of such units in the complex taking place as between their respective CO and CH2 groups in the alternative enolic form CH-C(OH). This view gives expression to the genetic relations of the celluloses to the ligno-celluloses, to the tendency to carbon condensation as in the formation of coals, and pseudo-carbons, to the relative resistance of cellulose to hydrolysis, and its other points of differentiation from starch, and more particularly to the ketonic character of its carbonyl (CO) groups, which is also more in harmony with the experimental facts established by Fenton as to the production of methyl furfural. The probability, however, is that no simple molecular formula adequately represents the constitution of cellulose as it actually exists or indeed reacts. On the other hand, it has been suggested that cellulose is to be regarded as representing a condition of matter analogous to that of a saline electrolyte in solution, i.e. as a complex of molecular aggregates, and of r
PREV.   NEXT  
|<   425   426   427   428   429   430   431   432   433   434   435   436   437   438   439   440   441   442   443   444   445   446   447   448   449  
450   451   452   453   454   455   456   457   458   459   460   461   462   463   464   465   466   467   468   469   470   471   472   473   474   >>   >|  



Top keywords:

cellulose

 

complex

 

formula

 

dextrose

 
regarded
 
Fenton
 

relations

 

formulated

 

dimensions

 

groups


reacting

 

simple

 

taking

 

methyl

 

celluloses

 

furfural

 

C6H10O5

 
molecular
 

solution

 

production


hydrolysis
 
esters
 

representing

 

linking

 

suggested

 

enolic

 

respective

 
condition
 

alternative

 

saline


oxygen

 
linkings
 

aggregates

 
easily
 

derived

 

analogous

 
expression
 
electrolyte
 

matter

 

differentiation


established

 

probability

 

points

 

postulated

 

starch

 

experimental

 
carbonyl
 

character

 
ketonic
 

resistance