The Synthesis of Benzothiazole Polymers with Perpendicularly Attached Phenyl Substituents

1988 ◽  
Vol 134 ◽  
Author(s):  
William A. Feld ◽  
YiHua Chang ◽  
John D. Peak ◽  
Scott G. Wierschke ◽  
Join Pin Chen

ABSTRACTA series of 2-aryl-4,7-benzothiazoledicarboxylic acids have been synthesized from the corresponding dimethyl derivatives. These derivatives contain the phenyl, and the p-bromo-, mchloro-, p-chloro-, m-methoxy-, and p-methoxyphenyl aryl substituents. The phenyl, pchlorophenyl and p-methoxyphenyl substituted diacids were polymerized with 2,5-diamino-1,4- benzenedithiol dihydrochloride to yield the corresponding poly(benzothiazole)s. The polymers were of low molecular weight (intrinsic viscosity as high as 1.7) and did not show enhanced solubility in common solvents.

1968 ◽  
Vol 12 (9) ◽  
pp. 2105-2109 ◽  
Author(s):  
P. Hague ◽  
M. B. Huglin ◽  
B. L. Johnson ◽  
J. Smith

1947 ◽  
Vol 20 (1) ◽  
pp. 1-13
Author(s):  
C. S. Marvel ◽  
W. J. Bailey ◽  
G. E. Inskeep

Abstract 1. A convenient laboratory procedure for the sodium-catalyzed copolymerization of butadiene and styrene has been described. Earlier attempts to accomplish this probably failed because the monomers were not sufficiently pure. 2. The copolymer of butadiene and styrene which results from sodium polymerization is different from the emulsion copolymer, GR-S, in several important respects. The sodium-catalyzed copolymer has a more nearly constant styrene content at different stages of conversion; it is made up of molecules with a relatively narrow molecular weight spread; it has a higher intrinsic viscosity; it is 100 per cent soluble in benzene (i.e., there is no gel) even at 100 per cent conversion; when treated with standard rubber antioxidant, it ages better; and it has a greater amount of the butadiene joined in the 1,2 manner (i.e., greater vinyl side-chain content). 3. The effects of such variables as temperature of polymerization, method of adding the monomer mixture to the catalyst, size of catalyst particles, and possible butadiene impurities on the polymerization have been studied. 4. The method has been extended to cover copolymerization of butadiene and m-methylstyrene to give a soluble copolymer of low molecular weight. Other styrene-type monomers gave less interesting copolymers.


2019 ◽  
Vol 21 (4) ◽  
pp. 738-747 ◽  
Author(s):  
Murray B. McBride ◽  
Sabrina E. Kelch ◽  
Michael P. Schmidt ◽  
Sonam Sherpa ◽  
Carmen Enid Martinez ◽  
...  

Here we study the precipitation of lead (Pb)-phosphate minerals over the pH range of 4.0 to 8.0 with and without oxalate, a ubiquitous and abundant low-molecular-weight organic acid derived from plants and microorganisms.


1979 ◽  
Vol 13 (10) ◽  
pp. 1104-1104 ◽  
Author(s):  
T. M. Karaputadze ◽  
V. I. Svergun ◽  
S. V. Tarabakin ◽  
V. P. Panov ◽  
Yu. �. Kirsh

Author(s):  
Clément Saidou ◽  
Jean Bosco Tchatchueng ◽  
Robert Ndjouenkeu ◽  
Denis CD Roux

In an attempt to understand the potential valorisation of local African legumes, hydrocolloids of five legumes (Corchorus olithorus, Triumfetta cordifolia, Cerathoteca sesamoides, Adansona digitata, and Bridelia thermifolia) were extracted and characterised as polysaccharides. All the gum extracted were rich in galactose residue (31-62 percent), suggesting a galactan backbone for the polysaccharides structure. The other sugar residues of the polysaccharides were arabinose (22-30 percent) in T. cordifolia and B. thermifolia, glucose (22-36 percent) in B. thermofolia, A. digitata and C. olithorus, and mannose (32.9 percent) in C. sesamoides. The intrinsic viscosity measurements showed that gums from T. cordifolia, B. thermifolia, C sesamoides and C. olithorus are high molecular weight polymers, while A. digitata contains low molecular weight polymers. The gum extracts also showed oil/water emulsion activity and were able to keep 60-90 percent of the emulsion stable on heating.


1955 ◽  
Vol 33 (10) ◽  
pp. 1491-1501 ◽  
Author(s):  
J. L. Gardon ◽  
S. G. Mason

Conductivity, dyestuff adsorption, and viscosity measurements on aqueous solutions of fractionated ligninsulphonate samples having various molecular weights indicate that they behave as flexible polyelectrolytes. There is evidence that ligninsulphonates of molecular weight less than 5000 associate in solution in a manner analogous to micelle formation in colloidal electrolytes. From the variation of intrinsic viscosity with molecular weight, it may be concluded that the degree of molecular branching of the high molecular weight ligninsulphonates is greater than that of the low molecular weight fractions.


1989 ◽  
Vol 5 (6) ◽  
pp. 1711-1718 ◽  
Author(s):  
M. H. Godinho ◽  
M. J. Seurin ◽  
P. Maïssa ◽  
P. Sixou

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