Researches on Cellulose, 1895-1900

Researches on Cellulose, 1895-1900

Researches on Cellulose, 1895-1900In the period 1895-1900, which has elapsed since the original publication of our work...
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Author: Bevan, E. J. (Edward John),1856-1921
Format: eBook
Language: English
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Researches on Cellulose, 1895-1900

Researches on Cellulose, 1895-1900

¥2,000 ¥1,000

Researches on Cellulose, 1895-1900

¥2,000 ¥1,000
Author: Bevan, E. J. (Edward John),1856-1921
Format: eBook
Language: English

Researches on Cellulose, 1895-1900

In the period 1895-1900, which has elapsed since the original publication of our work on 'Cellulose,' there have appeared a large number of publications dealing with special points in the chemistry of cellulose. So large has been the contribution of matter that it has been considered opportune to pass it under review; and the present volume, taking the form of a supplement to the original work, is designed to incorporate this new matter and bring the subject as a whole to the level to which it is thereby to be raised. Some of our critics in reviewing the original work have pronounced it 'inchoate.' For this there are some explanations inherent in the matter itself. It must be remembered that every special province of the science has its systematic beginning, and in that stage of evolution makes a temporary 'law unto itself.' In the absence of a dominating theory or generalisation which, when adopted, gives it an organic connection with the general advance of the science, there is no other course than to classify the subject-matter. Thus 'the carbohydrates' may be said to have been in the inchoate condition, qualified by a certain classification, prior to the pioneering investigations of Fischer. In attacking the already accumulated and so far classified material from the point of view of a dominating theory, he found not only that the material fell into systematic order[Pg 2] and grew rapidly under the stimulus of fruitful investigation, but in turn contributed to the firmer establishment of the theoretical views to which the subject owed its systematic new birth. On the other hand, every chemist knows that it is only the simpler of the carbohydrates which are so individualised as to be connoted by a particular formula in the stereoisomeric system. Leaving the monoses, there is even a doubt as to the constitution of cane sugar; and the elements of uncertainty thicken as we approach the question of the chemical structure of starch. This unique product of plant life has a literature of its own, and how little of this is fully known to what we may term the 'average chemist' is seen by the methods he will employ for its quantitative estimation. In one particular review of our work where we are taken to task for producing 'an aggravating book, inchoate in the highest degree ... disfigured by an obscurity of diction which must materially diminish its usefulness' ['Nature,' 1897, p. 241], the author, who is a well-known and competent critic, makes use of the short expression in regard to the more complex carbohydrates, 'Above cane sugar, higher in the series, all is chaos,' and in reference to starch, 'the subject is still enshrouded in mystery.' This 'material' complexity is at its maximum with the most complex members of the series, which are the celluloses, and we think accounts in part for the impatience of our critic. 'Obscurity of diction' is a personal quantity, and we must leave that criticism to the fates. We find also that many workers whose publications we notice in this present volume quite ignore the plan of the work, though they make use of its matter. We think it necessary to restate this plan, which, we are satisfied, is systematic, and, in fact, inevitable. Cellulose is in the first instance a structure, and the anatomical relationships supply a certain basis of classification. Next, it is known to us and is defined[Pg 3] by the negative characteristics of resistance to hydrolytic actions and oxidations. These are dealt with in the order of their intensity. Next we have the more positive definition by ultimate products of hydrolysis, so far as they are known, which discloses more particularly the presence of a greater or less proportion of furfural-yielding groups. Putting all these together as criteria of function and composition we find they supply common or general dividing lines, within which groups of these products are contained. The classification is natural, and in that sense inevitable; and it not only groups the physiological and chemical facts, but the industrial also. We do not propose to argue the question whether the latter adds any cogency to a scientific scheme. We are satisfied that it does, and we do not find any necessity to exclude a particular set of phenomena from consideration, because they involve 'commercial' factors. We have dealt with this classification in the original work (p. 78), and we discuss its essential basis in the present volume (p. 28) in connection with the definition of a 'normal' cellulose. But the 'normal' cellulose is not the only cellulose, any more than a primary alcohol or an aliphatic alcohol are the only alcohols. This point is confused or ignored in several of the recent contributions of investigators. It will suffice to cite one of these in illustration. On p. 16 we give an account of an investigation of the several methods of estimating cellulose, which is full of valuable and interesting matter. The purpose of the author's elaborate comparative study is to decide which has the strongest claims to be regarded as the 'standard' method. They appear to have a preference for the method of Langeviz. that of heating at high temperatures (180) with alkaline hydrates, but the investigation shows that (as we had definitely stated in our original work, p. 214) this is subject to large and variable errors. The adverse judgment of the authors, we may[Pg 4] point out, is entirely determined on the question of aggregate weight or yield, and without reference to the ultimate composition or constitution of the final product. None of the available criteria are applied to the product to determine whether it is a cellulose (anhydride) or a hydrate or a hydrolysed product. After these alkali-fusion processes the method of chlorination is experimentally reviewed and dismissed for the reason that the product retains furfural-yielding groups, which is, from our point of view, a particular recommendation, i.e. is evidence of the selective action of the chlorine and subsequent hydrolysis upon the lignone group. As a matter of fact it is the only method yet available for isolating the cellulose from a lignocellulose by a treatment which is quantitatively to be accounted for in every detail of the reactions. It does not yield a 'normal' cellulose, and this is the expression which, in our opinion, the authors should have used. It should have been pointed out, moreover, that, as the cellulose is separated from actual condensed combination with the lignone groups, it may be expected to be obtained in a hydrated form, and also not as a homogeneous substance like the normal cotton cellulose. The product is a cellulose of the second group of the classification. Another point in this investigation which we must criticise is the ultimate selection of the Schulze method of prolonged maceration with nitric acid and a chlorate, followed by suitable hydrolysis of the non-cellulose derivatives to soluble products. Apart from its exceptional inconvenience, rendering it quite impracticable in laboratories which are concerned with the valuation of cellulosic raw materials for industrial purposes, the attack of the reagent is complex and ill-defined. This criticism we would make general by pointing out that such processes quite ignore the specific characteristics of the non-cellulose components of the compound celluloses. The second division of the plan of our[Pg 5] work was to define these constituents by bringing together all that had been established concerning them. These groups are widely divergent in chemical character, as are the compound celluloses in function in the plant. Consequently there is for each a special method of attack, and it is a reversion to pure empiricism to expect any one treatment to act equally on the pectocelluloses, lignocelluloses, and cutocelluloses. Processes of isolating cellulose are really more strictly defined as methods of selective and regulated attack of the groups with which they occur, combined or mixed. A chemist familiar with such types as rhea or ramie (pectocellulose), jute (lignocellulose), and raffia (cutocellulose) knows exactly the specific treatment to apply to each for isolating the cellulose, and must view with some surprise the appearance at this date of such 'universal prescriptions' as the process in question. The third division of our plan of arrangement comprised the synthetical derivatives of the celluloses, the sulphocarbonates first, as peculiarly characteristic, and then the esters, chiefly the acetates, benzoates, and nitrates. To these, investigators appear to have devoted but little attention, and the contribution of new matter in the present volume is mainly the result of our own researches. It will appear from this work that an exhaustive study of the cellulose esters promises to assist very definitely in the study of constitutional problems. This brings us to the fourth and, to the theoretical chemist, the most important aspect of the subject, the problem of the actual molecular structure of the celluloses and compound celluloses. It is herein we are of opinion that the subject makes a 'law unto itself.' If the constitution of starch is shrouded in mystery and can only be vaguely expressed by generalising a complex mass of statistics of its successive hydrolyses, we can only still more vaguely guess at[Pg 6] the distance which separates us from a mental picture of the cellulose unit. We endeavour to show by our later investigations that this problem merges into that of the actual structure of cellulose in the mass. It is definitely ascertained that a change in the molecule, or reacting unit, of a cellulose, proportionately affects the structural properties of the derived compounds, both sulphocarbonates and esters. This is at least an indication that the properties of the visible aggregates are directly related to the actual configuration of the chemical units. But it appears that we are barred from the present discussion of such a problem in absence of any theory of the solid state generally, but more particularly of those forms of matter which are grouped together as 'colloids.' ......Buy Now (To Read More)

Product details

Ebook Number: 22620
Author: Bevan, E. J. (Edward John)
Release Date: Sep 16, 2007
Format: eBook
Language: English

Contributors

Contributor (Author): Cross, C. F. (Charles Frederick), 1855-1935


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