Methods of testing plastics. Determination of butyl rubber content of acetone-soluble matter in phenolic moulding materials after moulding.

1978 ◽  
Keyword(s):  
2021 ◽  
Author(s):  
Ying Chen ◽  
Dong Yiyang ◽  
Xiang Ma ◽  
Jiaru Li ◽  
Minmin Guo ◽  
...  

Abstract Background: Taraxacum kok-saghyz (TKS), a plant native to the Tianshan valley on the border between China and Kazakhstan and inherently rich in natural rubber, inulin and other bioactive ingredients, is an important industrial crop. TKS rubber is a good substitute for natural rubber. TKS's breeding work necessitates the need to screen high-yielding varieties, hence rapid determination of rubber content is essential for the screening. Conventional analytical methods cannot meet actual needs in terms of real-time testing and economic cost. Near-infrared spectroscopy analysis technology, which has developed rapidly in the field of industrial process analysis in recent years, is a green detection technology with obvious merits of fast measurement speed, low cost and no sample loss. This research aims to develop a portable non-destructive near-infrared spectroscopic detection scheme to evaluate the content of natural rubber in TKS fresh roots. Pyrolysis gas chromatography (PyGC), was chosen as the reference method for the development of NIR prediction model. Results: 208 TKS fresh root samples were collected from the Inner Mongolia Autonomous Region of China. Near-infrared spectra were acquired for all samples. Randomly two-thirds of them were selected as the calibration set, the remaining one-third as the verification set, and the partial least squares method was successfully used to establish a good NIR prediction model at 1080-1800nm with a performance to deviation ratio (RPD) of 5.54 and coefficient of determination (R2) of 0.95. Conclusions: This study showed that portable near-infrared spectroscopy could be used with ease for large-scale screening of TKS plants in farmland, and could greatly facilitate TKS germplasm preservation, high-yield cultivation, environment-friendly, high-efficiency and low-cost rubber extraction, and comprehensive advancement of the dandelion rubber industry thereof.


1931 ◽  
Vol 4 (4) ◽  
pp. 601-611
Author(s):  
S. D. Gehman ◽  
J. S. Ward

Abstract It is desirable to devise a method for determining the dry rubber content of latex which will be both more rapid than the two trial coagulation methods and more precise than the hydrometric method. The turbidity of latex, depending upon the volumetric number and size of the suspended rubber particles, offers a satisfactory criterion for the determination of the rubber content of latex. A microturbidimeter, herein described, has been adapted to such determinations. It permits more rapid determinations of the rubber content than the two trial coagulation methods. Its precision is less than the lengthy trial coagulation method, involving coagulation, creping, and drying, but is probably greater than that of the shortened trial coagulation method involving only coagulation and creping. Its precision is approximately 1 per cent rubber in 35 per cent latex. The turbidity of latex obeys the turbidity-dilution law for rubber-content values less than 15 per cent. The use of color filters, transmitting the shorter wave lengths of light, minimizes the effects of a difference in the effective mean particle size of different kinds of latex.


2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Min Zhao ◽  
Xianhui Li ◽  
Di Zhang ◽  
Longshan Zhao

Objective. To establish a method for extraction and determination of antioxidant 264 (2,6-di-tert-butyl-4-methylphenol) in the brominated butyl rubber stopper for injection and migration study in recombinant potent antitumor and antivirus protein injection (Novaferon). Methods. Dichloromethane-ethanol was adopted as the extraction solvent during the process of reflux extraction of antioxidant 264 in the brominated butyl rubber stopper. High-performance liquid chromatography (HPLC) was used for the determination of the migration of antioxidant 264 to Novaferon. The mobile phase consisted of acetonitrile-water (80 : 20, v/v). The flow rate was 1.5 mL/min. The detection wavelength was 280 nm. Results. The linearity range was from 4.003 to 200.150 μg/mL (r2 = 0.99996), and the average recovery of antioxidant 264 was 97.8%. The applicability of the methodology was good, which can be used for the determination of antioxidant 264. The results indicated that antioxidant 264 was not detected in Novaferon after the accelerated test and three months of long-term test. Conclusion. The established validated method in this study can be used for the determination of antioxidant 264 in the rubber stopper, and the brominated butyl rubber stopper has good compatibility with Novaferon.


1958 ◽  
Vol 31 (1) ◽  
pp. 82-85
Author(s):  
D. Barnard

Abstract The preparation of graft and block interpolymers of natural rubber and synthetic polymers has made it desirable that the number and size of polymer chains attached to rubber be readily determinate. The degradation of unsaturated polymers with tert-butyl hydroperoxide in the presence of osmium tet oxide has been used for the determination of free polystyrene in SBR and carbon black in several elastomers, and has recently been applied to the present problem. The accurate determination of the rubber content of interpolymers by quantitative ozonolysis essentially according to the method of Boer and Kooyman suggested that this might be made the basis of isolation of the attached polymer, the rubber being degraded into fragments of low molecular weight, from which the polymer could be separated by conventional techniques. The method should be applicable to any interpolymer, or mixture, of a polyunsaturated and a saturated polymer and is illustrated with reference to interpolymers of natural rubber (NR)-polymethyl methacrylate (PMM) and NR-polystyrene (PS).


2013 ◽  
Vol 45 ◽  
pp. 44-51 ◽  
Author(s):  
Sunisa Suchat ◽  
Daniel Pioch ◽  
Serge Palu ◽  
Eric Tardan ◽  
Eibertus Nicolaas van Loo ◽  
...  

Author(s):  
David J.T. Hill ◽  
James H. O'Donnell ◽  
M.C. Senake Perera ◽  
Peter J. Pomery

2014 ◽  
Vol 87 (4) ◽  
pp. 664-678 ◽  
Author(s):  
Leticia Saiz-Rodríguez ◽  
José María Bermejo-Muñoz ◽  
Andrés Rodríguez-Díaz ◽  
Alberto Fernández-Torres ◽  
Antonio Rubinos-Pérez

ABSTRACT Thermogravimetric analysis (TGA) and 14C techniques were compared for the determination of the biomass content of end-of-life tires (ELTs). Samples of different types (of ELTs) were prepared, and the biomass fraction of each sample was measured using the two methods (TGA and 14C). Six reference samples were also prepared with known quantities of natural rubber and stearic acid in order to establish the calibration curve necessary for the thermogravimetric analysis and to verify the accuracy of the results of the 14C analysis. The conclusions were that the 14C technique is the more valid, reliable, and precise method for determining the biomass content of end-of-life tires, since the results of the 14C tests of the reference samples coincided perfectly with the actual natural rubber and stearic acid content. On the other hand, the results of the thermogravimetric method differed considerably from the known natural rubber content of the reference samples as well as from the results of the 14C technique. This method is therefore not appropriate for use in determining the biomass content of end-of-life tires.


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