Samples and sampling of vegetable oil
Official Monthly Bulletin Interstate Cotton Seed Crushers' Association
33
(CttEMISTS' SECTION)
F u r t h e r examples are unnecessary, though abundantly
available; the above will be sufficient to illustrate forcibly the need for such work whereby the obvious shortcomings of the laboratory departments in this field be
eliminated and uniformity of results Oll fertilizer work
be brought up to as high a plane as that to which work
on meals has been developed.
In an effort to locate the causes of these discrepancies
apart from the personal equation of the individual analyst, a certain small share in the responsibility may be
attributed to the extreme difficulty in preparing samples
on a large scale having consistent uniformity throughout. The thorough mixing of a large batch of dry material presents many practical difficulties. In spite of
great care and special precautions taken in their preparation, a reasonable amount of error in their uniformity
is to be expected in the case of some samples, in view
of the heterogeneity of the material it is necessary to
use- in some cases. But, on the other hand, the greatest
probable error due to even a carelessly prepared sample
is far less than the variations reported from which the
above quotations are taken.
Further examination of the situation appears to point
to the probability of' the trouble arising from the variations possible in the analytical procedure. Thus in one
standard method alone for the determination of Total
Phosphoric Acid no less than seven different optional
methods are prescribed for the operation of getting the
sample into solution. In the same method three different
procedures are given for the determ4na,tion. In this
way there are 21 distinctly different methods of procedure, each one being reliably accurate for its own particularly suitable application, but presenting large possibilities for error under unsuitable circumstances.
These circumstances are at the discretion of the chemist,
and it may be safely said that the discretion of many
chemists is unequal to the strain.
In planning the fertilizer series for the coming season
these contingencies were taken into account, and provisions made to compensate for them, leaving the results of the season's work as completely dependent on
the proficiency of the analyst as it is physically practicable to attain.
In the preparation of samples the moral pointed by
past experience will be given a full measure of consideration. Only those materials will be used for samples
whose nature is such as to allow of the preparation of
dependable samples. The grinding and sifting a n d mixing of the material will be carried out to the most scrupulous degree in all stages of the process, special machinery having been developed to assist in attaining these
ends, and recent experience has demonstrated that the
equipment available is entirely adequate for the rather
severe demands made upon it.
To eliminate the difficulties arising from the use of
different schemes of analysis it has been decided to issue.
with every sample, definite detailed directions for making the determinations called for, and each chemist participating will be required to analyze the sample in accordance with those directions, regardless of the method
he may have found most advantageous in his particular
line of work.
CORRECTION
OF T O M P K I N S '
REPORT
SAMPLING
On page 29 of our December issue there appeared an
article by Mr. P. W. Tompkins entitled "Samples and
Sampling of Vegetable Oil." Due to an error in making the drawing there are a number of discrepancies between the cut and the wording of the paper. This Mr.
Tompkins calls attention to as follows:
The sketch of the omeial 10" sampling tubes on
page 30 for the B and C tubes should be reversed.
In other words, the one marked C is in reality B,
and the one m a r k e d ]3 is in reality C in all referenees in the article.
Also, page 31, line 2, should read:
Figure C when used as a ]0" sampling tube, instead of Figure ]3.
Page 31, 3d paragraph, 4th line, should read:
Moves as readily as the valve in Figure E instead
of Figure C, as published.
RUBBERSEED
OIL
By H. P. Trevithick and M. F. Lauro, N e w York
P r o d u c e Exchange
This oil is obtained from the seeds of the para rubber
tree, a native of Brazil.
This seed has been in great demand for starting para
rubber trees in the East but the demand has lessened so
that the seeds are available for oil. Our sample came
from the Orient:
P e r cent
Color--Reddish Brown.
Appearance--Slightly Turbid.
Specific Gravity at 15.5 ~ C . . . . . . . . . . . . . . . .
Iodine Value ( W i j s ) . . . . . . . . . . . . . . . . . . . . .
Saponification Value . . . . . ". . . . . . . . . . . . . . . .
Acid Value . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Free Fatty Acids . . . . . . . . . . . . . . . . . . . . . . . .
Index of Refraction at 25 o C . . . . . . . . . . . . . .
Titre - ~ C . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Unsaponifiable Matter . . . . . . . . . . . . . . . . . . .
Acetyl Value . . . . . . . . . . . . . . . . . . . . . . . . . . .
0.9250
137.8
192.2
34~3
17.14
1.4733
28.8
0.95
30.6
The oil dries fairly hard in 54 hours, but does not
dry as hard as linseed oil. It should be a fair substitute for linseed oil.
M I N E R A L OIL C O N T A M I N A T I O N
C O T T O N S E E D OIL
By R. H. Fash
OF
Not infrequently samples of crude cottonseed oil are
encountered, which, on refining, yield a yellow oil
usually off in color and having a strong fluorescence.
The presence of this fluorescent appearance has usually
been considered as indicating mineral oil contamination.
and has been eliminated from the oil produced by a
mill by stopping lubricating oil leaks into the seeds or
meats. In order to determine the amount of lubricating
oil necessary to produce an off colored, fluorescent oil
from a prime colored cottonseed oil, known amounts of
a lubricating oil that was being used to lubricate the
rolls of a mill that was producing crude cottonseed oil,
which, on refining, gave an off colored fluorescent yellow oil, were added to definite quantities of prime colored, non-fluorescent yellow oil. The resultant mixtures
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