An Emulsion Polymerization Process for Soluble and Electrically Conductive Polyaniline

1997 ◽  
Vol 488 ◽  
Author(s):  
P. J. Kinlen ◽  
Y. Ding ◽  
C. R. Graham ◽  
J. Liu ◽  
E. E. Remsen
Keyword(s):  
Molecular Weight ◽  
Organic Acid ◽  
Organic Solvents ◽  
Organic Phase ◽  
Sulfonic Acid ◽  
Direct Synthesis ◽  
Water Soluble ◽  
Polymerization Process ◽  
Phase System ◽  
Two Phase

AbstractA new emulsion process has been developed for the direct synthesis of the emeraldine salt of polyaniline (PANI) that is soluble in organic solvents. The process entails forming an emulsion composed of water, a water soluble organic solvent (e.g., 2-butoxyethanol), a water insoluble organic acid (e.g., dinonylnaphthalene sulfonic acid) and aniline. Aniline is protonated by the organic acid to form a salt which partitions into the organic phase. As oxidant (ammonium peroxydisulfate) is added, PANI salt forms in the organic phase and remains soluble. As the reaction proceeds, the reaction mixture changes from an emulsion to a two phase system, the soluble PANI remaining in the organic phase. With dinonylnaphthalene sulfonic acid (DNNSA) as the organic acid, the resulting product is truly soluble in organic solvents such as xylene and toluene(not a dispersion), of high molecular weight (Mw >22,000), film forming and miscible with many polymers such as polyurethanes, epoxies and phenoxy resins. As cast, the polyaniline film is only moderately conductive, (10−5 S/cm), however treatment of the film with surfactants such as benzyltriethylammonium chloride (BTEAC) or low molecular weight alcohols and ketones such as methanol and acetone increases the conductivity 2–3 orders of magnitude.

scholarly journals The interphase distribution of light REE Ce(III) and La(III) in system based on PEG-1500 – NaNO3 – H2O with the quaternary ammonium base addition

2022 ◽  
Vol 1212 (1) ◽  
pp. 012023
Author(s):  
A V Levina ◽  
A Ya Fedorov ◽  
M I Fedorova
Keyword(s):  
Organic Solvents ◽  
Quaternary Ammonium ◽  
Water Solution ◽  
Distribution Coefficients ◽  
Water Soluble ◽  
Process Time ◽  
Phase System ◽  
Two Phase ◽  
Quaternary Ammonium Base ◽  
Promising Alternative

Abstract The problem of e-waste processing and recovery of valuable metals from such waste for the second use is attracting more and more scientists’ attention. Liquid extraction as one of hydrometallurgy steps is a traditional method for the metal recovery. However, application of solvent extraction is not meet the green chemistry principles due to organic solvents. Aqueous two-phase systems based on water-soluble polymers are promising alternative for hazardous organic solvents. In this work the dependencies of Ce(III) and La(III) distribution coefficients from process time and the initial quaternary ammonium base concentration have been achieved. Also, based on the Ce(III) and La(III) extraction isotherms it has been shown that the metals initial concentrations are highly affects the distribution coefficients of studied metals. The possibility of aqueous two-phase system application as a solvent for quaternary ammonium salt for light REE (Ce(III) and La(III)) extraction from water solution has been shown.

Optimization of Aqueous Two Phase Extraction of Proteins from Litopenaeus Vannamei Waste by Response Surface Methodology Coupled Multi-Objective Genetic Algorithm

2019 ◽  
Vol 15 (1) ◽  
Author(s):  
P. Saravana Pandian ◽  
S. Sindhanai Selvan ◽  
A. Subathira ◽  
S. Saravanan
Keyword(s):  
Genetic Algorithm ◽  
Molecular Weight ◽  
Response Surface Methodology ◽  
Response Surface ◽  
Litopenaeus Vannamei ◽  
Value Added ◽  
Phase System ◽  
Two Phase ◽  
Multi Objective ◽  
Multi Objective Genetic Algorithm

Abstract Waste generated from industrial processing of seafood is an enormous source of commercially valuable proteins. One among the underutilized seafood waste is shrimp waste, which primarily consists of head and carapace. Litopenaeus vannamei (L. vannamei) is the widely cultivated shrimp in Asia and contributes to 90 % of aggregate shrimp production in the world. This work was focused on extraction as well as purification of value-added proteins from L. vannamei waste in a single step aqueous two phase system (ATPS). Polyethylene glycol (PEG) and trisodium citrate system were chosen for the ATPS owing to their adequate partitioning and less toxic nature. Response surface methodology (RSM) was implemented for the optimization of independent process variables such as PEG molecular weight (2000 to 6000), pH (6 to 8) and temperature (25 to 45 °C). The results obtained from RSM were further validated using a Multi-objective genetic algorithm (MGA). At the optimized condition of PEG molecular weight 2000, pH 8 and temperature 35 °C, maximum partition coefficient and protein yield were found to be 2.79 and 92.37 %, respectively. Thus, L. vannamei waste was proved to be rich in proteins, which could be processed industrially through cost-effective non-polluting ATPS extraction, and RSM coupled MGA could be a potential tool for such process optimization.

Glycosidases in organic solvents: I. Alkyl-β-glucoside synthesis in a water-organic two-phase system

1990 ◽  
Vol 12 (12) ◽  
pp. 950-954 ◽  
Author(s):  
Evgeni N. Vulfson ◽  
Rooma Patel ◽  
Jean E. Beecher ◽  
Anthony T. Andrews ◽  
Barry A. Law
Keyword(s):  
Organic Solvents ◽  
Phase System ◽  
Two Phase

scholarly journals THE LIMITING MECHANISM IN TARSAL CHEMORECEPTION

1951 ◽  
Vol 35 (1) ◽  
pp. 55-65 ◽  
Author(s):  
V. G. Dethier
Keyword(s):  
Partition Coefficients ◽  
Physiological Effect ◽  
Threshold Concentration ◽  
Water Soluble ◽  
Phormia Regina ◽  
Phase System ◽  
Primary Alcohols ◽  
Two Phase ◽  
The Relationship ◽  
Gain Access

Rejection thresholds of eight primary alcohols applied to the tarsal chemoreceptors of the blowfly Phormia regina Meigen and the ovipositor of Gryllus assimilis Fab. have been determined. Three different solvents for the alcohols have been used: water, ethylene glycol, and mineral oil. The comparative stimulating effectiveness of the alcohols assumes a different aspect with each different solvent. In oil the range of thresholds from methanol to octanol extends over less than one log unit as compared with the corresponding thresholds in water which extend over four log units. In glycol the thresholds extend over two and one half log units only. When water is employed as a solvent, the line which describes the relationship between threshold concentration and chain length of the compound exhibits a sharp break at or near butanol. No such discontinuity is evident when glycol or oil is employed as solvent. This is offered as evidence supporting the hypothesis that the limiting mechanism in tarsal chemoreception involves a two phase system whereby highly water-soluble compounds gain access to the receptor through an aqueous phase and the larger lipoid-soluble molecules chiefly through a lipoid phase. Additional facts which support this idea are gained from data which show that the inflection in the curve occurs at different points with different species of insects and is conspicuously absent in the case of man. When thresholds in aqueous solutions are converted from molar concentrations to activities, it is clear that the relation of equal physiological effect at equal thermodynamic activities does not apply here. The lower members of the series stimulate at progressively increasing activities up to pentanol and then at progressively decreasing activities. Furthermore, the ratio of water threshold to oil threshold exhibits no obvious agreement with the water/oil partition coefficients determined experimentally. These results indicate either that the limiting process of chemoreception in these insects does not depend upon the establishment of an equilibrium or that some kinetic effect is obscuring an underlying relationship which does so depend.

Ruthenium(II) Ions triggered direct supramolecular polymerization of bis-terpyridine poly(ethylene glycol): New Insights on synthesis and optimization

e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Manuela Chiper ◽  
Richard Hoogenboom ◽  
Ulrich S. Schubert
Keyword(s):  
Molecular Weight ◽  
Ethylene Glycol ◽  
Direct Synthesis ◽  
Synthesis Method ◽  
Water Soluble ◽  
Poly Ethylene Glycol ◽  
Full Characterization ◽  
Vis Spectroscopy ◽  
Poly Ethylene ◽  
The Stability

AbstractIn order to obtain linear and high molecular weight Ru(II) coordination polymers, we investigated the reaction conditions for the direct one-step metallopolymerization of bis-terpyridine poly(ethylene glycol) 3 with RuCl3 in the presence of reducing agents. Here we discuss the direct synthesis method, the optimization and the purification of the water soluble Ru(II) chain extended poly(ethylene glycol). The optimization of the metallo-polymerization was monitored by SEC. For the highest molecular weight Ru(II) coordination polymer 4 obtained in this study, full characterization was performed by 1H-NMR and UV-Vis spectroscopy as well as SEC proof for the formation and the stability of the designed structure

scholarly journals Wasserlösliche Phosphane, III [1]. Wasserlösliche primäre Phosphane mit Ammoniumgruppierungen NR2R' in der Seitenkette -donorfunktionalisierte Amphiphile / Water-Soluble Phosphanes, III [1]. Water-Soluble Primary Phosphanes with Ammonium Groups NR2R' in the Side Chain -Donor-Functionalized Amphiphiles

1994 ◽  
Vol 49 (11) ◽  
pp. 1511-1524 ◽  
Author(s):  
David J. Brauer ◽  
Jörg Fischer ◽  
Stefan Kucken ◽  
Klaus P. Langhans ◽  
Othmar Stelzer ◽  
...  
Keyword(s):  
Water Solubility ◽  
Water Soluble ◽  
Side Chain ◽  
Phase System ◽  
Alkyl Side Chain ◽  
Two Phase ◽  
Trans Conformation ◽  
Phosphonous Acid ◽  
X Ray ◽  
Superbasic Medium

Primary and secondary aminoalkylphosphanes R2N-(CH2)m-PH2 (R2 = Me2, nBu2, C5H10, C4H8O, 2-(1-Methyl-2-pyrrolidinyl); m = 2, 3, 6, 10, 11; 1-6) or [R2N-(CH2)m]2PH (7, R2 = C5H10; m = 2) are accessible by aminoalkylation of PH3 with ω̃ -chloroalkylamines R2N-(CH2)m-Cl in the superbasic medium DMSO/KOH (DMSO = dimethylsulfoxide). By selective N-quaternization of 1, 2, 4-6 with R'I (R' = Me, CnH2n+1; n = 6-8, 12, 16, 18) in the two-phase system CH2Cl2/H2O novel primary phosphanes [R'R2N-(CH2)m-PH2]+I- (11-16f) with quaternary ammonium groups in the alkyl side chain are obtained. The water solubility of 11-16f decreases with increasing chain length (n) of R′ 11 (R = R' = Me; m = 2) shows a trans conformation at the C2H4 bridge according to an X-ray structural analysis. Protonation of 1, 2, 4, 5 with HCl affords the water-soluble hydrochlorides [HR2N-(CH2)m-PH2]+Cl- (19-22). The cationic primary phosphanes 11-16f are stable towards oxygen. By oxidation of 11 with one or two equivalents of H2O2 the primary phosphane oxide [Me3N-(CH2)2-P(O)H2]+I- (23) or the phosphonous acid [Me3N-(CH2)2- P(O)(OH)H]+I- (23a) are formed. Hofmann degradation of 11 or 16c with KOH yields phosphirane in good yields. Reaction of 1, 2, 4-6 (L) with Fe2(CO)9 at ambient temperature yields stable complexes (CO)4FeL (26-30). Under more rigorous conditions Fe3 clusters (31, 32) with free R2N groups are obtained.

Study of Aqueous Two Phase System on Water Soluble Bio Oil

2011 ◽  
Vol 236-238 ◽  
pp. 49-53
Author(s):  
Shao Peng Liu ◽  
Zhi Min Zong ◽  
Shan Shan Zhang ◽  
Yue Xu ◽  
Gui Zhen Gong ◽  
...  
Keyword(s):  
Lower Layer ◽  
Water Soluble ◽  
Extraction Rate ◽  
Phase System ◽  
Two Phase ◽  
Element Analysis ◽  
Aqueous Two Phase System ◽  
Bio Oil ◽  
Infrared Spectrometer ◽  
Aqueous Two Phase Extraction

This paper was aimed to study the aqueous two phase extraction (ATPE) on water soluble bio oil(SBO), in which ethanol, K2HPO4, NaH2PO4and (NH4)2SO4were selected to form the water soluble bio oil(SBO) aqueous two phase system (ATPS). After phase separation, the extraction rates and the volume ratios of the upper to lower layer of the ATPSs were investigeted. Both the upper and lower layers of these SBO ATPSs were analyzed by elemental analyzer and Fourier transformation infrared spectrometer (FTIR). The different extraction rates indicates the influnces of different salt during the phase saperation, of which NaH2PO4has less effect to SBO than the other two; K2HPO4may neutralize some organic acid; the lowest extraction rate of ethanol/(NH4)2SO4system indicates the effects of (NH4)2SO4to SBO. Too much ethanol will fech in more water, hence the optimizational ratio of the SBO ATPS should be SBO:salt:ethanol=10:10:5. In element analysis, the diclining of oxygen in all the upper layers and the increasing of nitrogion in both layers of (NH4)2SO4system indicates the abbility of the less oxygen components concentration of the ATPS and the reaction between (NH4)2SO4and SBO. According to FTIR test, the lack of absorption at 1515cm-1of all the lower layers indicates the completely transforming of phenols into the upper layers. Because of the high extraction rate and less influence to SBO, ethanol/NaH2PO4system may be the most suitable ATPS for SBO extraction.

scholarly journals Recovery of steroidal glucosiduronic acids from organic solvents containing anionic liquid ion-exchangers

1972 ◽  
Vol 126 (3) ◽  
pp. 545-552 ◽  
Author(s):  
Vernon R. Mattox ◽  
Robert D. Litwiller ◽  
June E. Goodrich
Keyword(s):  
Organic Solvents ◽  
Aqueous Phase ◽  
Organic Phase ◽  
Biological Fluids ◽  
Phase 1 ◽  
Primary Amines ◽  
Ion Exchangers ◽  
Two Phase ◽  
Organic Solutions ◽  
Solubilizing Effect

Solutions of anionic liquid ion-exchangers in organic solvents are potentially useful for extracting steroidal glucosiduronic acids from biological fluids and for purifying mixtures of these acids by chromatography. If a glucosiduronic acid is to be isolated in pure form after either of these procedures, it is necessary to separate it from the ion-exchanger. Separation from an organic solution of tetraheptylammonium chloride may be accomplished by extraction with water under the following conditions, which promote transfer of a glucosiduronate to the aqueous phase: (1) an appropriate solvent (diluent) as the organic phase, (2) the presence in the two-phase mixture of an anion such as myristate or dodecyl sulphate to combine with the tetraheptylammonium ion, and (3) an increase of the pH of the aqueous phase in association with the presence of myristate or dodecyl sulphate. The foregoing factors apply also to removal of glucosiduronates from organic solutions of ion exchangers that are hydrochlorides of tertiary, secondary, or primary amines. Since these amines exert progressively less solubilizing effect for glucosiduronates as the pH of the aqueous phase is increased, the conjugates can be released from the organic phase by adjusting the pH to 10 and omitting the myristate or dodecyl sulphate.

Sign in / Sign up

Export Citation Format

Share Document