Formation Mechanism of Polyaniline Nanostructures in PEG Solution

2013 ◽  
Vol 652-654 ◽  
pp. 182-187
Author(s):  
Dan Zhang

Nano structured polyaniline was intensively studied for its low price, fascinating tunable conductive properties by dope-dedope process. While the nanostructural formation mechanism still not clear. In this work, PANI nanostructures were obtained in acidity PEG solution, and the polymerization process was monitored by a pH instrument. Moreover, the morphology evolution was monitored, based on which a self-assemble mechanism was issued. The oxidation products of anilinium cations were consider as the seed template for the formation of nanostructures, and appropriate acidity is propitious to the formation of PANI nanostructures.

1960 ◽  
Vol 33 (3) ◽  
pp. 636-638 ◽  
Author(s):  
V. A. Kropachev ◽  
B. A. Dolgoplosk ◽  
N. I. Nikolaev

Abstract It has been established by a number of studies that the chain structure in the catalytic polymerization of monoolefins and dienes is determined to a large degree by the nature of the catalytic complex, participating in the polymerization process. Also it was shown that the initial catalytic complex bears a direct relationship to each elementary act of the chain growth. The isolation of organolithium compounds in the pure state is associated with great experimental difficulties. Together with the formation of the organometal compounds the possibility of a complex mixture of their oxidation products being formed is not excluded. To elucidate the influence of the indicated oxidation products on the chain structure in the polymerization of butadiene it seemed expedient to investigate the influence of oxygen. As the result of the investigation made by us it was established that in the polymerization of 1,3-butadiene with organolithium compounds the introduction of comparatively small amounts of oxygen into the system leads to a substantial increase in the number of 1,2 units in the polybutadiene at the expense of a reduction in the number of 1,4 units. The addition of either alcohol or phenol exerts a similar influence on the structure of the polymeric chain (Table 1).


RSC Advances ◽  
2016 ◽  
Vol 6 (109) ◽  
pp. 107829-107835 ◽  
Author(s):  
Yanqiu Lei ◽  
Haiquan Su ◽  
Rongkai Tian

Hydrochar spheres were formed by the condensation, polymerization and pyrolysis behavior of hemicellulose, amorphous cellulose and soluble lignin.


RSC Advances ◽  
2016 ◽  
Vol 6 (85) ◽  
pp. 81559-81568 ◽  
Author(s):  
Bingrong Dong ◽  
Nan Shen ◽  
Chuanxiang Cao ◽  
Zhang Chen ◽  
Hongjie Luo ◽  
...  

To reveal the formation mechanism of VO2 nanomaterials in a hydrothermal system, a novel method was proposed to study the influence of ammonium (NH4+) on the growth of VO2 nanomaterial.


1974 ◽  
Vol 31 (02) ◽  
pp. 309-318
Author(s):  
Phyllis S Roberts ◽  
Raphael M Ottenbrite ◽  
Patricia B Fleming ◽  
James Wigand

Summary1. Choline chloride, 0.1 M (in 0.25 M Tris. HCl buffer, pH 7.4 or 8.0, 37°), doubles the rate of hydrolysis of TAME by bovine thrombokinase but has no effect on the hydrolysis of this ester by either human or bovine thrombin. Only when 1.0 M or more choline chloride is present is the hydrolysis of BAME by thrombokinase or thrombin weakly inhibited. Evidence is presented that shows that these effects are due to the quaternary amine group.2. Tetramethyl ammonium bromide or chloride has about the same effects on the hydrolysis of esters by these enzymes as does choline chloride but tetra-ethyl, -n.propyl and -n.butyl ammonium bromides (0.1 M) are stronger accelerators of the thrombokinase-TAME reaction and they also accelerate, but to a lesser degree, the thrombin-TAME reaction. In addition, they inhibit the hydrolysis of BAME by both enzymes. Their effects on these reactions, however, do not follow any regular order. The tetraethyl compound is the strongest accelerator of the thrombokinase-TAME reaction but the tetra-ethyl and -butyl compounds are the strongest accelerators of the thrombin-TAME reaction. The ethyl and propyl compounds are the best (although weak) inhibitors of the thrombokinase-BAME and the propyl compound of the thrombin-BAME reactions.3. Tetra-methyl, -ethyl, -n.propyl and -n.butyl ammonium bromides (0.01 M) inhibit the clotting of fibrinogen by thrombin (bovine and human proteins) at pH 7.4, imidazole or pH 6.1, phosphate buffers and they also inhibit, but to a lesser degree, a modified one-stage prothrombin test. In all cases the inhibition increases regularly as the size of the alkyl group increases from methyl to butyl. Only the ethyl com pound (0.025 M but not 0.01 M), however, significantly inhibits the polymerization of bovine fibrin monomers. It was concluded that inhibition of the fibrinogen-thrombin and the one-stage tests by the quaternary amines is not due to any effect of the com pounds on the polymerization process but probably due to inhibition of thrombin’s action on fibrinogen by the quaternary amines.


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