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Hexadecyltrimethylammonium Bromide (hexadecyltrimethylammonium + bromide)
Selected AbstractsAdsorbing colloid flotation for removal of metal ions in waters from base metal minesENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 1 2002H. Sabti Adsorbing Colloid Flotation (ACF) has been shown in laboratory experiments to be effective for the removal of heavy metals (Zn, Cu, Cd and Pb) from dilute solutions. Sodium dodecyl sulphate (SDS) and sodium oleate (NaOl) were used as surfactants in single or mixed form, with Fe(OH)3 as a flocculant for colloid formation. These reagents worked best for zinc and copper ions for a feed concentration of 50 parts per million (ppm). The removal of lead improved significantly by the use of Fe(OH)3 and NaLS (Sodium lauryl sulphate), while the best removal of cadmium was achieved by the use of Al(OH)3 and HTMABr (hexadecyltrimethylammonium bromide). Flotation experiments were conducted with feed concentrations of 50 and 500 parts per billion (ppb) and 50 ppm (parts per million). The experimental results showed that the residual concentration of metal ions decreased significantly with the decrease in the feed concentration. This could be the effect of excessive (much more than stoichiometric ratio) amounts of surfactant and flocculant, compared to the feed concentrations, required in the effective flotation of dilute feed solutions. The surfactant concentration and feed pH had the largest effects on the process, as observed in the case of cadmium removal. This can be attributed to the flocformation and flotation tendencies of the colloid-metal complexes at various solution pH and surfactant concentrations. The ACF method was applied to a number of natural drainage solutions from the metal mines at Te Aroha, New Zealand, and the experimental results demonstrate that significant removal is achieved for most of the heavy metals. [source] Effect of self-assemblies of various surfactants in their single and mixed states on the BZ oscillatory reactionINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 11 2010Muzaffar Hussain Najar Micelles of different surfactants are well known to affect chemical equilibria and reactivities by selectively sequestering the reagent substrates through electrostatic and hydrophobic interactions. In this article, the effects of micelles of various surfactants on different parameters of the Ce(IV)-catalyzed Belousov,Zhabotinsky (BZ) oscillatory reaction at 35°C in nonstirred closed conditions are studied by employing spectrophotometry and tensiometry. Surfactants used in this study are the cationics hexadecyltrimethylammonium bromide (CTAB) and pentamethylene-1,5-bis(N -hexadecyl- N,N -dimethylammonium)bromide gemini (Gemini), anionic sodium dodecylbenzene sulfonate (SDBS), and nonionic Brij58, whereas the binary surfactant systems used are cationic,nonionic CTAB+Brij58 and anionic,nonionic SDBS+Brij58. The results revealed that the induction period shows a definite variation with increasing concentration of different surfactants above their critical micelle concentration (cmc). The amplitudes of oscillation and absorbance maxima and minima are enhanced in the presence of micelles of CTAB and Gemini surfactants, whereas micelles of SDBS and Brij58 have almost no effect on the nature of the oscillations. However, mixed micelles of CTAB+Brij58 and SDBS+Brij58 binary mixtures show a quite different effect on the overall behavior of the oscillations. The enhanced effect of CTAB and Gemini surfactants on the overall nature of oscillations has been attributed to the positive charge on the surface of their micelles and to some extent on the presence of nitrogen in their head group. The effect of mixed binary micelles may be attributed to their synergistic nature. © 2010 Wiley Periodicals, Inc. Int J Chem Kinet 42: 659,668, 2010 [source] Metallomicelle catalysis: Hydrolysis of p -nitrophenyl picolinate induced by Schiff base Co(II) complexes in a Gemini surfactant micellar solutionINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 12 2007Weidong Jiang Two Schiff base cobalt(II) complexes containing crowned substituents have been synthesized and employed to promote the hydrolysis of p -nitrophenyl picolinate (PNPP) in a buffered micellar solution formed by a cationic Gemini surfactant, bis(hexadecyldimethylammonium)hexane bromide (G(hex)C16, 2Br,) over a pH range of 6.50,8.50. In comparison, the reactivity of PNPP hydrolysis catalyzed by the same catalysts in the other micellar system, formed by a conventional single-chain analogue, that is, hexadecyltrimethylammonium bromide (CTAB), has also been evaluated under a selected condition. The results clearly reveal that the two metallomicelles made of the aforementioned Co(II) complexes and the G(hex)C16 are both efficient for catalyzing PNPP hydrolysis with about 3 orders of magnitude in rate acceleration compared with the background rate of PNPP spontaneous hydrolysis. Moreover, the rates of PNPP hydrolysis catalyzed by the two cobalt(II) complexes in G(hex)C16 micelles are about 2 times higher than in CTAB micelles, correspondingly. In addition, observations show that steric hindrance of substituents of the two complexes is also one of the major influencing factors in the PNPP hydrolytic reaction. © 2007 Wiley Periodicals, Inc. Int J Chem Kinet 39: 672,680, 2007 [source] Two-dimensional electrophoresis with cationic detergents, a powerful tool for the proteomic analysis of myelin proteins.JOURNAL OF NEUROSCIENCE RESEARCH, Issue 4 2008Part 1: Technical aspects of electrophoresis Abstract The analysis of proteins in damaged myelin is crucial to clarify the mechanisms of dysmyelination and demyelination. In the present study, proteomic analysis of myelin using a modified two-dimensional electrophoresis (2-DE) method was carried out to obtain a better understanding of myelin biology. Although standard 2-DE (immobilized pH gradient isoelectric focusing/sodium dodecyl sulfate-polyacrylamide gel electrophoresis; IPG/SDS-PAGE) methods of analysis provide high resolutions of soluble proteins with isoelectric focusing points in the pH range of 4,8, major myelin components include highly basic proteins are compacted at the basic edge of the 2-DE gels and are not sufficiently separated for satisfactory analysis. In an attempt to improve the separation of these proteins, an alternative 2-DE method using the cationic detergents was applied. In part 1 of this study, we describe technical aspects of conditioning 2-DE using cationic detergent. In the accompanying paper (part 2), practical 2-DE analysis using cationic detergents is described to identify proteins in the purified CNS myelin fraction. We carried out benzyldimethyl- n -hexadecylammonium chloride (16-BAC)/SDS-PAGE 2-DE and tested 2-DE with four other cationic detergents. We found that 16-BAC was the most effective agent for separation of myelin proteins and that hexadecyltrimethylammonium bromide (cetyltrimethylammonium bromide; CTAB) was the most effective agent for solubilization of myelin proteins. The combination of 16-BAC/SDS-PAGE and CTAB/SDS-PAGE is a powerful tool for the analysis of myelin proteins, including highly basic, high-MW (MW > 100K), and integral membrane proteins. © 2007 Wiley-Liss, Inc. [source] In situ ethylene homopolymerization and copolymerization catalyzed by zirconocene catalysts entrapped inside functionalized montmorilloniteJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 14 2003Chengbin Liu Abstract Ethylene homopolymerizations and copolymerizations were catalyzed by zirconocene catalysts entrapped inside functionalized montmorillonites that had been rendered organophilic via the ion exchange of the interlamellar cations of layered montmorillonite with hydrochlorides of L -amino acids (AAH+Cl,) or their methyl esters (MeAAH+Cl,), with or without the further addition of hexadecyltrimethylammonium bromide (C16H33N+Me3Br,; R4N+Br,). In contrast to the homogeneous Cp2ZrCl2/methylaluminoxane catalyst for ethylene homopolymerizations and copolymerizations with 1-octene, the intercalated Cp2ZrCl2 activated by methylaluminoxane for ethylene homopolymerizations and copolymerizations with 1-octene proved to be more effective in the synthesis of polyethylenes with controlled molecular weights, chemical compositions and structures, and properties, including the bulk density. The effects of the properties of the organic guests on the preparation and catalytic performance of the intercalated zirconocene catalysts were studied. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2187,2196, 2003 [source] Oxidation and chemiluminescence of catechol by hydrogen peroxide in the presence of Co(II) ions and CTAB micellesLUMINESCENCE: THE JOURNAL OF BIOLOGICAL AND CHEMICAL LUMINESCENCE, Issue 5 2007Jan Lasovsky Abstract The oxidation of catechol in neutral and slightly alkaline aqueous solutions (pH 7,9.6) by excess hydrogen peroxide (0.002,0.09 mol/L) in the presence of Co(II) (2.10,7,2.10,5 mol/L) is accompanied by abrupt formation of red purple colouration, which is subsequently decolourized within 1 h. The electron spectra of the reaction mixture are characterized by a broad band covering the whole visible range (400,700 nm), with maximum at 485 nm. The reaction is initiated by catechol oxidation to its semiquinone radical and further to 1,2-benzoquinone. By nucleophilic addition of hydrogen peroxide into the p -position of benzoquinone C=O groups, hydroperoxide intermediates are formed, which decompose to hydroxylated 1,4-benzoquinones. It was confirmed by MS spectroscopy that monohydroxy-, dihydroxy- and tetrahydroxy-1,4-benzoquinone are formed as intermediate products. As final products of catechol decomposition, muconic acid, its hydroxy- and dihydroxy-derivatives and crotonic acid were identified. In the micellar environment of hexadecyltrimethylammonium bromide the decomposition rate of catechol is three times faster, due to micellar catalysis, and is accompanied by chemiluminescence (CL) emission, with maxima at 500 and 640 nm and a quantum yield of 1 × 10,4. The CL of catechol can be further sensitized by a factor of 8 (maximum) with the aid of intramicellar energy transfer to fluorescein. Copyright © 2007 John Wiley & Sons, Ltd. [source] Synthesis of Large-Area Three-Dimensional Polyaniline Nanowire Networks Using a "Soft Template"MACROMOLECULAR RAPID COMMUNICATIONS, Issue 5 2005Wenbin Zhong Abstract Summary: Three-dimensional polyaniline (PANI) nanowire networks were synthesized in high yield using a "soft template" self-assembled with hexadecyltrimethylammonium bromide and oxalic acid. The PANI nanowire networks had diameters from 35,100 nm depending on synthesis conditions and/or procedures. The networks and the "cross-linking points" were clearly observed by field-emission scanning electron microscopy and transmission electron microscopy. A possible mechanism for the formation of three-dimensional PANI nanowire networks is discussed. FESEM image of PANI with three-dimensional nanowire networks. [source] An effective DNA extraction protocol for brown algaePHYCOLOGICAL RESEARCH, Issue 2 2001Naomi Phillips SUMMARY Successful extraction of total DNA from brown algae, which are generally polysaccharide and polyphenol rich, is often problematic using current methods. Persistent polysaccharide and polyphenolic compounds can hinder further application of modern molecular techniques requisite to molecular-based evolutionary studies. Our broad and long-term research goals with fucalean taxa, especially Sargassum, and problems with existing DNA extraction methods were an impetus to develop a reliable DNA extraction method. Initial research established hexadecyltrimethylammonium bromide (CTAB) based total-DNA methods as the most viable for further empirical development. Several constituents effective at either complexing secondary compounds or creating a reductive extraction environment were increased in concentration or added to the extraction buffer. These seemingly minor changes resulted in the creation of a highly reductive extraction buffer and effective total- DNA harvesting technique. We detail these modifications and demonstrate the reliability of the modified protocol with a variety of brown algae and tissue preservation methods. Such DNA is shown to be suitable for a variety of molecular techniques. [source] Solubilization of Single-Walled Carbon Nanotubes by using Polycyclic Aromatic Ammonium Amphiphiles in Water,Strategy for the Design of High-Performance SolubilizersCHEMISTRY - A EUROPEAN JOURNAL, Issue 15 2006Yasuhiko Tomonari Abstract We describe the design of polycyclic aromatic compounds with high performance that dissolve single-walled carbon nanotubes (SWNTs). Synthetic amphiphiles trimethyl-(2-oxo-2-phenylethyl)-ammonium bromide (1) and trimethyl-(2-naphthalen-2-yl-2-oxo-ethyl)-ammonium bromide (2) carrying a phenyl or a naphtyl moiety were not able to dissolve/disperse SWNTs in water. By contrast, trimethyl-(2-oxo-2-phenanthren-9-yl-ethyl)-ammonium bromide (3) solubilized SWNTs, although the solubilization ability was lower than that of trimethyl-(2-oxo-2-pyrene-1-yl-ethyl)-ammonium bromide (4) (solubilization behavior observed by using 4 was described briefly in reference 4a). Transmission electron microscopy (TEM), as well as visible/near-IR, fluorescence, and near-IR photoluminescence spectroscopies were employed to reveal the solubilization properties of 4 in water, and to compare these results with those obtained by using sodium dodecyl sulfate (SDS) and hexadecyltrimethylammonium bromide (HTAB) as solubilizers. Compound 4 solubilized both the as-produced SWNTs (raw-SWNTs) and purified SWNTs under mild experimental conditions, and the solubilization ability was better than that of SDS and HTAB. Near-IR photoluminescence measurements revealed that the chiral indices of the SWNTs dissolved in an aqueous solution of 4 were quite different from those obtained by using micelles of SDS and HTAB; for a SWNTs/4 solution, the intensity of the (7,6), (9,5), and (12,1) indices were strong and the chirality distribution was narrower than those of the micellar solutions. This indicates that the aqueous solution of 4 has a tendency to dissolve semiconducting SWNTs with diameters in the range of 0.89,1.0 nm, which are larger than those SWNTs (0.76,0.97 nm) dissolved in the aqueous micelles of SDS and HTAB. [source] | ||||||||||||||||