The Coagulation of Latices by Polar-Nonpolar Liquids

1938 ◽  
Vol 11 (1) ◽  
pp. 87-91
Author(s):  
F. K. Daniel ◽  
H. Freundlich ◽  
K. Söllner

Abstract (1) Diluted latices—Abiarana gutta-percha latex was specially investigated—may be coagulated by shaking them with organic liquids, not miscible with water in all proportions, provided that the liquids form a second liquid phase and that their molecules have a polar-nonpolar structure (butyl alcohol, isobutyric acid, cyclohexanol, etc.). Nonpolar liquids (petroleum ether, chloroform, etc.) do not coagulate diluted latices on shaking under these conditions. (2) This coagulating action can be explained by assuming that the latex particles are strongly accumulated at the interfaces of polar-nonpolar liquids and water; this is not the case with nonpolar liquids. (3) Small concentrations of some polar-nonpolar substances of small molecular weight, soluble in water, can also coagulate Abiarana gutta-percha latex if they form unstable foams; this was observed with propanol and isopropanol. If the foam formed under these conditions is stable, as with small concentrations of dissolved butanol and isobutanol, no coagulation takes place. This behavior can be explained as in (2), the air bubbles behaving like the second liquid phase. (4) Jelutong latex is known to contain an excess of resins, compared with the amount of rubber. A method of coagulating this latex quickly and separating the resins from the rubber consists in shaking the latex for some seconds with certain polar-nonpolar liquids, forming a second liquid phase, such as isobutyl or isoamyl alcohol. A lump of rubber is accumulated at the interface of the two liquids; the resins are contained in the organic phase.

Biologia ◽  
2019 ◽  
Vol 75 (1) ◽  
pp. 139-149
Author(s):  
Venkatesh Bommalapura Kulkarni ◽  
Raghu Ram Achar ◽  
Maheshwari Mahadevappa ◽  
Dinesh Sosalagere Manjegowda ◽  
Priya Babu Shubha ◽  
...  

e-Polymers ◽  
2021 ◽  
Vol 21 (1) ◽  
pp. 491-499
Author(s):  
Fukai Yang ◽  
Hao Yu ◽  
Yuyuan Deng ◽  
Xinyu Xu

Abstract In this article, five kinds of soybean oil-based polyols (polyol-E, polyol-P, polyol-I, polyol-B, and polyol-M) were prepared by ring-opening the epoxy groups in epoxidized soybean oil (ESO) with ethyl alcohol, 1-pentanol, isoamyl alcohol, p-tert-butylphenol, and 4-methoxyphenol in the presence of tetrafluoroboric acid as the catalyst. The SOPs were characterized by FTIR, 1H NMR, GPC, viscosity, and hydroxyl numbers. Compared with ESO, the retention time of SOPs is shortened, indicating that the molecular weight of SOPs is increased. The structure of different monomers can significantly affect the hydroxyl numbers of SOPs. Due to the large steric hindrance of isoamyl alcohol, p-hydroxyanisole, and p-tert-butylphenol, SOPs prepared by these three monomers often undergo further dehydration to ether reactions, which consumes the hydroxyl of polyols, thus forming dimers and multimers; therefore, the hydroxyl numbers are much lower than polyol-E and polyol-P. The viscosity of polyol-E and polyol-P is much lower than that of polyol-I, polyol-B, and polyol-M. A longer distance between the molecules and the smaller intermolecular force makes the SOPs dehydrate to ether again. This generates dimer or polymers and makes the viscosity of these SOPs larger, and the molecular weight greatly increases.


RSC Advances ◽  
2016 ◽  
Vol 6 (35) ◽  
pp. 29326-29333 ◽  
Author(s):  
Abdul G. Al Lafi ◽  
James N. Hay

Thermal history and purification effects on the structural properties of PVK were investigated. Liquid–liquid phase separation is suggested to occur by separation of isotactic rich segments from a matrix which is predominantly atactic.


1974 ◽  
Vol 52 (3) ◽  
pp. 231-240 ◽  
Author(s):  
A. H. Warner ◽  
P. C. Beers ◽  
F. L. Huang

An enzyme that catalyzes the synthesis of P1P4-diguanosine 5′-tetraphosphate (Gp4G) has been isolated and purified from yolk platelets of encysted embryos of the brine shrimp, Artemia salina. The enzyme GTP:GTP guanylyltransferase (Gp4G synthetase) utilizes GTP as substrate, has a pH optimum of 5.9–6.0, a temperature optimum of 40–42 °C, and requires Mg2+ and dithiothreitol for optimal activity. The synthesis of Gp4G is inhibited markedly by pyrophosphate, whereas orthophosphate has no effect on the reaction. In the presence of GDP the enzyme also catalyzes the synthesis of P1,P3-diguanosine 5′-triphosphate (Gp3G), but the rate of synthesis is low compared with Gp4G synthesis and dependent upon other small molecular weight components of yolk platelets.


2010 ◽  
Vol 24 (5) ◽  
pp. 1373-1378 ◽  
Author(s):  
Juan Sun ◽  
Yan Wu ◽  
Zhuang Su ◽  
Zhifang Liu ◽  
Bingzhong Su ◽  
...  

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