UNTERSUCHUNGEN ÜBER VERSCHIEDENE BESTIMMUNGSMETHODEN DER CELLULOSE.

H. Suringar and B. Tollens (Ztschr. angew. Chem. 1896, No. 23).

INVESTIGATION OF METHODS OF DETERMINING CELLULOSE.

Introduction.—This is an exhaustive bibliography of the subject, describing also the various methods of cellulose estimation, noted in historical sequence. First, the Weende 'crude fibre' method (Henneberg) with modifications of Wattenberg, Holdefleiss, and others is dealt with. The product of this treatment, viz. 'crude fibre' is a mixture, containing furfuroids and lignone compounds. Next follows a group of processes which aim at producing a 'pure cellulose' by eliminating lignone constituents, for which the merely hydrolytic treatments of the Weende method are ineffectual. The method of F. Schulze—prolonged digestion with dilute nitric acid, with addition of chlorate—has been largely employed, though the composition of the product is more or less divergent from a 'pure cellulose.'

Dilute nitric acid at 60-80° (Cross and Bevan) and a dilute mixture of nitric and sulphuric acids (Lifschutz) have been employed for isolating cellulose from the lignocelluloses. Hoffmeister modifies the method of Schulze by substituting hydrochloric acid for the nitric acid. Treatment with the halogens associated with alkaline processes of hydrolysis is the basis of the methods of Hugo Muller (bromine water) and Cross and Bevan (chlorine gas). Lastly, the authors notice the methods based upon the action of the alkaline hydrates at high temperatures (180°) in presence of water (Lange), or of glycerin (Gabriel). The process of heating to 210° with glycerin only (Hönig) yields a very impure and ill-defined product.

For comparative investigation of these processes certain celluloses and cellulosic materials were prepared as follows:

(a) 'Rag' cellulose.—A chemical filter paper, containing only cotton and linen celluloses, was further purified by boiling with dilute acid and dilute alkali. After thorough washing it was air-dried.

(b) Wood cellulose.—Pine wood sawdust was treated by digestion for fourteen days with dilute nitric acid with addition of chlorate (Schulze). The mass was washed and digested with alkaline lye (1.25 p.ct. KOH), and exhaustively washed, treated with dilute acetic acid; again washed, and finally air-dried.

This product was found to yield 2.3 p.ct. furfural on distillation with HCl (1.06 sp.gr.).

(c) Purified wood.—Pine wood sawdust was treated in succession with dilute alkalis and acids, in the cold, and with alcohol and ether until exhausted of products soluble in these liquids and reagents.

In addition to the above the authors have also employed jute fibre and raw cotton wool in their investigations.

They note that the yield of cellulose is in many cases sensibly lowered by treating the material after drying at the temperature of 100°. The material for treatment is therefore weighed in the air-dry condition, and a similar sample weighed off for drying at 100° for determination of moisture.

The main results of the experimental investigation are as follows:—

Weende process further attacks the purified celluloses as follows: Wood cellulose losing in weight 8-9 p.ct.; filter paper, 6-7.5 p.ct., and the latter treated a second time loses a further 4-5 p.ct. It is clear, therefore, that the process is of purely empirical value.

Schulze.—This process gave a yield of 47.6 p.ct. cellulose from pine wood. The celluloses themselves, treated by the process, showed losses of 1-3 p.ct. in weight, much less therefore than in the preceding case.

Hönig's method of heating with glycerin to 210° was found to yield products very far removed from 'cellulose.' The process may have a certain value in estimations of 'crude fibre,' but is dismissed from further consideration in relation to cellulose.

Lange.—The purpose of the investigation was to test the validity of the statement that the celluloses are not attacked by alkaline hydrates at 180°. Experiments with pine wood yielded a series of percentages for cellulose varying from 36 to 41; the 'purified wood' gave also variable numbers, 44 to 49 per cent. It was found possible to limit these variations by altering the conditions in the later stages of isolating the product; but further experiments on the celluloses themselves previously isolated by other processes showed that they were profoundly and variably attacked by the 'Lange' treatment, wood cellulose losing 50 per cent. of its weight, and filter paper (cellulose) losing 15 per cent. Further, a specimen of jute yielded 58 per cent. of cellulose by this method instead of the normal 78 per cent. It was also found that the celluloses isolated by the process, when subjected to a second treatment, underwent a further large conversion into soluble derivatives, and in a third treatment further losses of 5-10 per cent were obtained. The authors attach value, notwithstanding, to the process which they state to yield an 'approximately pure cellulose,' and they describe a modified method embodying the improvements in detail resulting from their investigation.

Gabriel's method of heating with a glycerin solution of alkaline hydrate is a combination of 'Hönig' and 'Lange.' An extended investigation showed as in the case of the latter that the celluloses themselves are more or less profoundly attacked by the treatment—further that the celluloses isolated from lignocelluloses and other complex raw materials are much 'less pure' than those obtained by the Lange process. Thus, notably in regard to furfural yielding constituents, the latter yield 1-2 p.ct. furfural, whereas specimens of 'jute cellulose' obtained by the Gabriel process were found to yield 9 to 13 p.ct. furfural.

Cross and Bevan.—Chlorination process yielded in the hands of the authors results confirming the figures given in 'Cellulose' for yield of cellulose. Investigation of the products for yield of furfural, gave 9 p.ct. of this aldehyde showing the presence of celluloses, other than the normal type.

Conclusions.—The subjoined table gives the mean numerical results for yield of end-product or 'cellulose' by the various methods. In the case of the 'celluloses' the results are those of the further action of the several processes on the end-product of a previous process.

Methods
F. Schulze Weende Lange Gabriel Cross and Bevan
Wood cellulose 98.51 91.52 48.22 55.93
Filter paper cellulose 99.62 95.63 78.17 79.77
Swedish filter paper 96.58 84.76
Ordinary filter paper 98.17 93.39 86.58
Cotton ('wool') 98.38 89.98 63.96 67.88
Jute 57.93 71.64 75.27
Purified wood{49.27
{46.56
Raw wood 47.60{40.82
{38.87

The final conclusion drawn from the results is that none of the processes fulfil the requirements of an ideal method. Those which may be carried out in a reasonably short time are deficient in two directions: (1) they yield a 'cellulose' containing more or less oxycellulose; (2) the celluloses themselves are attacked under the conditions of treatment, and the end product or cellulose merely represents a particular and at the same time variable equilibrium, as between the resistance of the cellulose and the attack of the reagents employed; this attack being by no means confined to the non-cellulose constituents. Schulze's method appears to give the nearest approximation to the 'actual cellulose' of the raw material.


(p. 8) SOLUTIONS OF CELLULOSE—(1) ZINC CHLORIDE.—To prepare a homogeneous solution of cellulose by means of the neutral chloride, a prolonged digestion at or about 100° with the concentrated reagent is required. The dissolution of the cellulose is not a simple phenomenon, but is attended with hydrolysis and a certain degree of condensation. The latter result is evidenced by the formation of furfural, the former by the presence of soluble carbohydrates in the solution obtained by diluting the original solution and filtering from the reprecipitated cellulose. The authors have observed that in carefully conducted experiments cotton cellulose may be dissolved in the reagent, and reprecipitated with a loss of only 1 p.ct. in weight. This, however, is a 'net' result, and leaves undetermined the degree of hydration of the recovered cellulose as of hydrolysis of the original to groups of lower molecular weights. Bronnert finds that a previous hydration of the cellulose—e.g. by the process of alkaline mercerisation and removal of the alkali by washing—enables the zinc chloride to effect its dissolution by digestion in the cold. (U.S. patent, 646,799/1900. See also p. 59.)

Industrial applications.—(a) Vulcanised fibre is prepared by treating paper with four times its weight of the concentrated aqueous solution (65-75° B.), and in the resulting gelatinised condition is worked up into masses, blocks, sheets, &c., of any required thickness. The washing of these masses to remove the zinc salt is a very lengthy operation.

To render the product waterproof the process of nitration is sometimes superadded [D.R.P. 3181/1878]. Further details of manufacture are given in Prakt. Handbuch d. Papierfabrikation, p. 1703 [C. Hofmann].

(b) Calico-printing.—The use of the solution as a thickener or colour vehicle, more especially as a substitute for albumen in pigment styles, was patented by E. B. Manby, but the process has not been industrially developed [E.P. 10,466 / 1894].

(c) Artificial silk.—This is a refinement of the earlier applications of the solution in spinning cellulose threads for conversion into carbon filaments for electrical glow-lamps. This section will be found dealt with on p. 59.

(p. 13) (2) Cuprammonium solution.—The application of the solution of cellulose in cuprammonium to the production of a fine filament in continuous length, 'artificial silk,' has been very considerably studied and developed in the period 1897-1900, as evidenced by the series of patents of Fremery and Urban, Pauly, Bronnert, and others. The subject will also be found dealt with on p. 58.


(p. 15) Reactions of cellulose with iodine.—In a recent paper, F. Mylius deals with the reaction of starch and cellulose with iodine, pointing out that the blue colouration depends upon the presence of water and iodides. In absence of the latter, and therefore in presence of compounds which destroy or absorb hydriodic acid—e.g. iodic acid—there results a brown addition product. The products in question have the characteristics of solid solutions of the halogen. (Berl. Ber. 1895, 390.)

(24) Mercerisation—Notwithstanding the enormous recent developments in the industrial application of the mercerising reaction, there have been no noteworthy contributions to the theoretical aspects of the subject. The following abstract gives an outline of the scope of an important technical work on the subject.