Contributions to the Analysis of Rubber. II. The Qualitative Determination of the Serum Components of Raw Rubber and of Vulcanized Rubber

1937 ◽  
Vol 10 (4) ◽  
pp. 716-724
Author(s):  
P. Dekker

Abstract The use of latex in the rubber industry has been increasing to a considerable extent, and in many cases where formerly solutions of ordinary plantation rubber were used exclusively, e. g., for impregnating fibres, spreading and adhering textiles, and manufacturing dipped goods, latex mixtures are now employed. Then again there is increasing interest in rubber prepared by evaporation or spraying of latex, especially for the production of powdered rubber. Consequently the time has come, as is evident from recent publications, when it may be an important problem whether in the preparation of a rubber mixture it is best to use ordinary plantation rubber, latex, or, perhaps, evaporated latex. Now the peculiarity of a rubber mixture prepared from latex or from evaporated latex is its relatively high precentage of serum substances from the latex. In the first Communication on the present subject, which dealt with the “Determination of the Water-Soluble Components of Rubber,” a method was described for determining the serum substances in vulcanized rubber. In view of the fact that with technical rubber mixtures, and in the presence of zinc, calcium, and magnesium compounds, this method is complicated and tedious, the present experiments were carried out with an aim to developing a procedure for determining qualitatively the serum substances. A method of this kind must naturally be restricted to the identification of some substance which originates in the serum and not in the curvatives or other compounding ingredients. Among the various substances which are present in latex serum, 1-methylinositol is one of the most important, and rubber mixtures prepared from latex or from evaporated latex contain a notable quantity of this substance. Consequently proof of the existence of 1-methylinositol in a mixture should be evidence of the presence of serum substances. The investigation to be described was therefore confined to the development of a characteristic reaction of 1-methylinositol.

1937 ◽  
Vol 10 (3) ◽  
pp. 574-583
Author(s):  
P. Dekker

Abstract 1. It is shown that the methods which are ordinarily used for determining water-soluble substances in raw rubber give low results, and are quite useless for vulcanized rubber. 2. New analytical procedures are developed for determining the water-soluble substances in raw rubber and in vulcanized rubber. These procedures are carried out in the following manner. (a) Raw Rubber.—Heat 2 grams of rubber in 80 cc. of xylene and 5 cc. of acetic acid on a water bath until the rubber is completely dissolved, add 5 cc. of acetic acid and 10 cc. of water, heat for 3–4 hours on the water bath with frequent agitation, transfer to a distilling flask (rinsing the first flask with 50 cc. of hot water), distill the xylene with steam, filter the residual solution, evaporate the filtrate on a water bath; and dry at 100° C. (b) Vulcanized Rubber and Rubber Mixtures.—First extract the sample with acetone, heat 2 grams of the acetone-extracted sample with 80 cc. of xylene on a water bath, add 5 cc. of acetic acid, reflux the mixture on an oil bath, after complete dissolution add 5 cc. of acetic acid and 10 cc. of water, heat the solution for 2 hours on an oil bath at 110–120° C., distill the xylene, as in the determination with raw rubber, filter the residue, evaporate the filtrate to dryness, take up the residue in 50 cc. of water, pass a current of hydrogen sulfide through the solution for 10 minutes to precipitate zinc as sulfide, filter, evaporate the filtrate, and dry the residue at 100° C. 3. In the presence of calcium compounds, magnesium compounds, glue and textiles, the method gives false results. Modifications of the method are therefore recommended, whereby these substances are eliminated.


2014 ◽  
Vol 77 (15-16) ◽  
pp. 1091-1102 ◽  
Author(s):  
Magdalena Buszewska-Forajta ◽  
Wiktoria Struck-Lewicka ◽  
Renata Bujak ◽  
Danuta Siluk ◽  
Roman Kaliszan

2021 ◽  
pp. 27-43
Author(s):  
Lilia Firdavisovna Gilmullina ◽  
Mira Leonidovna Ponomareva ◽  
Sergey Nikolayevich Ponomarev ◽  
Gul'naz Suleymanovna Mannapova

Arabinoxylans (AXs) – non-starch polysaccharides (NSPs)  is one of the most discussed main components contained in all parts of cereal plants. AXs combine bioactive and technological functions. As dietary fibres, they have physiologically beneficial properties for human health. AXs are water-soluble and insoluble in water. The structure, structure, quantity and properties of AXs depend on which part of the grain or cereal plant is extracted and which method of isolation is used. There are many different methods of preliminary and deep impact aimed at extraction of AXs from plant raw materials. The use of a simple method or complex treatment for quantitative and qualitative determination of AXs depends on objectives and possibilities. The overview provides data on AXs content of different crops, depending on the extraction method. The main classical methods of AXs extraction, their advantages, disadvantages, and possible limitations of use are described. The variants of calculation of the quantitative AXs content used by different authors are separately considered.


Molecules ◽  
2020 ◽  
Vol 25 (16) ◽  
pp. 3632
Author(s):  
Ho-Shin Huang ◽  
Hsu-Sheng Yu ◽  
Chia-Hung Yen ◽  
Ean-Tun Liaw

This study established a validated method for the quantitative and qualitative determination of eight signature compounds in Eccoilopus formosanus. We used multiple-reaction monitoring scanning for quantification, and switched the electrospray ion source polarity between positive and negative modes in a single chromatographic run. The precursor-to-product ion transitions were m/z 355/163, m/z 181/163, m/z 265/122, m/z 269/117, m/z 170/152, m/z 377.2/180.7, m/z 169/124.8 and m/z 193/134 for chlorogenic acid, caffeic acid, thiamine, apigenin, pyridoxamin, riboflavin, gallic acid and ferulic acid, respectively. The developed method was also validated for accuracy, precision and limit of quantification. In this method, eight compounds were quantified with correlation coefficients of greater than 0.995. A high recovery (81.5–94.1%) and good reproducibility was obtained for five phenolics and three vitamins with the relative standard deviation, ranging from 1.2 to 3.5%. This method may be applied to the determination of both phenolics and water-soluble vitamins in cereal grain. The results may suggest that the extract of E. formosanus could be a good source of bioactive phytochemicals.


1978 ◽  
Vol 39 (C6) ◽  
pp. C6-1232-C6-1233 ◽  
Author(s):  
N. F. Pedersen ◽  
J. Mygind ◽  
O. H. Soerensen ◽  
B. Dueholm

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


Author(s):  
Hind Hadi ◽  
Gufran Salim

A simple, rapid and sensitive spectrophotmetric method for trace determination of salbutamol (SAL) in aqueous solution and in pharmaceutical preparations is described. The method is based on the diazotization coupling reaction of the intended compound with 4-amino benzoic acid (ABA) in alkaline medium to form an intense orange, water soluble dye that is stable and shows maximum absorption at 410 nm. A graph of absorbance versus concentration indicates that Beer’s law is obeyed over the concentration range of 0.5-30 ppm, with a molar absorbtivity 3.76×104 L.mol-1 .cm-1 depending on the concentration of SAL. The optimum conditions and stability of the colored product have been investigated and the method was applied successfully to the determination of SAL in dosage forms.


Sign in / Sign up

Export Citation Format

Share Document