Academic literature on the topic 'Quaternary ammonium bromide (QBr)'

Quaternary ammonium compounds are broad-spectrum bacteriocides widely used as antiseptics, disinfection and preservation agents. The aim of this study was to examine the activity of two quaternary ammonium salts, cetylpyridinum bromide and a newly synthesized quaternary bis ammonium salt, against S. epidermidis biofilm. The average values of killing efficiency for cetylpyridinum bromide ranged from 26.6% to 64.1% for all tested concentrations (0.125 to 8.0 microg x mL(-1)) and for quaternary bis ammonium salt the percentage of killing efficiency ranged from 59.7% to 88.4% for tested concentrations (from 2.0 to 128.0 microg x mL(-1)). Both tested compounds significantly affect staphylococcal biofilms, but any of used concentrations caused a total eradication of bacterial biofilm.

The title compound, C13H18IN4 +·Br−·2H2O, is a quaternary ammonium salt derived from 2-iodobenzyl bromide and hexamethylenetetramine. Two water molecules per asymmetric unit act as hydrogen-bond donors to the bromide anion. Direct cation–anion contacts are established via C—H donors, mainly from methylene groups in the α position to the ammonium centre.

"Otilonium bromide (C29H43 N2 O4+.Br-) is a quaternary ammonium derivative which has been proven a potent spasmolytic drug with a good tolerability profile, used in the treatment of irritable bowel syndrome. We present herein the structural analysis of an unreported polymorphic form (I), comparing with the only one known so far and already reported [1] polymorphic form of the compound (II). The data set for I was obtained from a twinned specimen. The poor quality of the data thus available did not pose any problem in the structure resolution, but it did instead in refinement: the alkyloxy chains and ethyl branches in the quaternary ammonium groups needed some continuity restraints in their anisotropic displacement factors. In form II this effect appeared enhanced, ending up in unusually large anisotropic displacement parameters for most atoms in the chain. The main points of molecular disagreement reside in the torsion angles where the alkyloxy chains and quaternary ammonium groups leave the planar mainframe. The only notorious intermolecular contacts in both structures appear to be a number of rather weak C–H···Br ones involving the quaternary ammonium groups somehow ""wrapping"" the bromide counterion. There are a few C–H···O contacts interlinking molecules to each other. The phase transformation occurs at 124(2)°C and can be followed by DSC and XRPD. A detailed analysis shows some features in common, viz., in both structures packing stability is mainly due to the ionic interaction between the N+ and the Br-, with the latter ion being evenly surrounded by a number of ammonium groups in a way that they define regular 2D arrays "sandwiching" the neutral part of the molecules, which thus act as spacers. These similarities allow giving a plausibility argument about the way in which the transition may take place."

Alkaline hydrolysis if the phenyl acetates CH3COOC6H4X (X = 4-NO2, 3-NO2, 3-Cl, H, 4-CH3, 3-CH3, and 4-OCH3) in the presence of hexadecyltris(2-hydroxyethyl)ammonium chloride, bis(2-hydroxyethyl)hexadecyl(methyl)ammonium bromide, and hexadecyltrimethylammonium bromide has been studied. Comparison of the rates of the hydrolysis for the above tenzides showed that the most efficient catalyst is the hexadecyltris(2-hydroxyethyl)ammonium chloride. In all cases, the rate data correlated well with structure effects by the Hammett equation.

Synthesis and antimicrobial properties of binaphthyl derived quaternary ammonium bromides(S)-N-(2-(4,5-dihydro-3H-dinaphtho[2,1-c:1',2'-e]azepin-1-yl)ethyl)-N, N-dimethyl-N-dodecyl ammonium bromide (S)-1a and (S)-N-(2-(4,5-dihydro-3H-dinaphtho[2,1-c:1',2'-e]azepin-1-yl)ethyl)-N, N-dimethyl-N-tetradecylammonium bromide (S)-1b have been synthesized as optically active quaternary ammonium salts starting from 1,1'-binaphthyl-2,2'-diol. Their antimicrobial activity expressed as minimal inhibition concentration (MIC) was tested against Gram-positive human pathogenic bacteria S. Aureus, Gram-negative bacteria E. coli and human fungal pathogen C. Albicans.

Hydrophlogopite was modified with sodium and then organically intercalated with a series of alkyl quaternary ammonium salts. The organically intercalated samples were characterized by X-ray diffraction analysis (XRD) and the effect of alkyl quaternary ammonium salt on the interlayer spacing of hydrophlogopite was discussed. The results showed that if the same alkyl quaternary ammonium salt was used to intercalate hydrophlogopite, the interlayer spacing of hydrophlogopite increased gradually with the rise of the added amount of quaternary ammonium salt, and that if different quaternary ammonium salts with the same amount were used, the interlayer spacing increased gradually with the rise of the chain length of the alkyl quaternary ammonium salts. For the alkyl quaternary ammonium salts with large chain length (n>10), the inflection point for the increasing interlayer spacing of the intercalated hydrophlogopite is at about 0.5 times of CEC. When octadecyl trimethyl ammonium bromide is used as intercalation agent and the added amount is 5 times of CEC, the interlayer spacing of hydrophlogopite is relatively maximal.

The Vanadium bromide (V/Br) flow cell employs the Br3-/Br- couple in the positive and the V(II)/V(III) couple in the negative half cell. One major issue of this flow cell is bromine gas formation in the positive half cell during charging which results from the low solubility of bromine in aqueous solutions. Bromine complexing agents previously used in the zinc-bromine fuel cell were evaluated for their applicability in V/Br flow cell electrolytes. Three quaternary ammonium bromides: N-ethyl-N-methyl-morpholinium bromide (MEM), N-ethyl-N-methyl-pyrrolidinium bromide (MEP) and Tetra-butyl ammonium bromide (TBA) were studied. It is known that aqueous bromine reacts with quaternary ammonium bromides to form an immiscible organic phase. Depending on the number of quaternary ammonium bromides used and the environmental temperature, the second phase formed will either be solid or liquid. As any solid formation would interrupt the flow cell operation, potential formation of such kind has to be eliminated. Stability tests of simulated V/Br electrolyte with added quaternary ammonium bromides were carried out at 11, 25 and 40 oC. In the absence of bromine, the addition of MEM, MEP and TBA were found to be stable in V/Br electrolytes. However, in the presence of bromine, solid formation was observed in the bromine rich organic phase when the V/Br electrolyte contained a single quaternary ammonium bromide (QBr) compound. For V/Br electrolytes with binary or ternary QBr mixtures containing TBA, the presence of bromine caused a viscous polybromide phase to form at room temperature and the release of bromine gas at higher temperature. Only a binary mixture of MEM and MEP formed a stable liquid organic phase between 11 ?? 40 oC. In this study it was found that V/Br electrolytes containing a binary QBr mixture (0.75M) of MEM and MEP gave the best combination that formed an orange oily layer in the presence of bromine without solidification between 11 ?? 40oC. Furthermore, it was found that samples of V/Br electrolytes containing a ternary QBr mixture, are less effective in bromine capturing if the total QBr concentration was less than 1 M at 40oC, where bromine gas evolution was observed. From electrochemical studies of V3+/V2+, it was found that the addition of MEM and MEP had a minimal effect on the formal potential of the V3+/V2+ couple, the V2+/V3+ transfer coefficient and the diffusion coefficient of V3+. Therefore, MEM and MEP can be added to the negative half-cell of a V/Br flow cell without major interference From linear sweep voltammetry, the kinetics of the Br-/Br3- redox couple was found to be mass transfer controlled. After the addition of MEM and MEP mixture, the exchange current density was found to decrease from 0.013 Acm-2 to 0.01 Acm-2. On the other hand the transfer coefficient before and after MEM and MEP addition was found to be 0.5 and 0.44 respectively. Since the kinetic parameters were not significantly affected by the addition of MEM and MEP mixture, they can be added to the positive half-cell of the V/Br flow cell as bromine complexing agents. The electrochemical studies of both V3+/V2+ and Br-/Br3- showed the addition of MEM and MEP has minimal interference with the redox reactions of the vanadium bromide flow cell. This thesis also investigated the effect of MEM and MEP addition on the cell performance of a lab scale V/Br flow cell using two different membranes (ChiNaf and VF11). Flow cell performance for 2 M V3.7+ + 0.19 M MEM + 0.56 M MEP electrolytes utilising ChiNaf membrane at 10 mAcm-2 produced an energy efficiency of 59%, and this decreased to 43% after 15 cycles. For the static cell utilising VF11 membrane, the addition of MEM and MEP reduced the energy efficiency from 59.7% to 43.4%. It is believed that this is caused by the mass transfer controlled Br-/Br3- couple in the complexed positive half-cell solution. Therefore, uniformity between the organic and aqueous phase is important for flow cells utilising electrolytes with MEM and MEP. Finally, the polarization resistance of a lab scale V/Br flow cell utilising ChiNaf membrane and 2 M V3.7+ electrolytes was found to be slightly higher during cell charging (3.9 cm2) than during the discharge process (3.6 cm2), which is opposed to that in the all-vanadium redox cell.

碩士
國立成功大學
化學工程研究所
85
This study amied at the formation of a third liquid phase and the reaction kinetics in the third liquid phase formed in the systems of toluene/R4NBr/(NaOPh+NaOH) aqueous solution. By a series of experiments, we have found that all symmetric quaternary ammonium bromides, except for Et4NBr, can form a third liquid phase. These symmetric quaternary ammonium salts can be classified into two types, hydrophilic and hydrophobic (lipophilic). In the system containing a hydrophihc salt, the third liquid phase was formed by salting-out effect with adding NaOH. Note that reverse extraction was observed in the system containing Bu4NBr. Referring to the result obtained by Angrawals et al., we know that this phenomenon is attributed to the formation of QOPh.(HOPh)n complex, in which phenol is formed by he hydrolysis of NaOPh. The formation this complex can enhance the solubility of QOPh in toluene. The formation of a third liquid phase in the system containing a hydrophobic salt is due to the formation of an ionic complex in toluene as explained in the following. From the IR spectrum, we know that the base complex in the toluene phase contains NaOPh, not NaOH. When an excess amount of base was found in toluene, more water was measured in the same phase. These two observations suggest the formation of QOPh.(H2O)n.(NaOPh)m complex in toluene. Futhermore, Na23 NMR spectrum shows that Na in this complex is of two types, ionic and nonionic (covalent). This fact implies that this complex might have ionic property which induce the formation of a third liquid phase. Temperature affects the formation of a third liquid phase in two different ways, depending the kind of quaternary ammonium salt. Low temperature is beneficial the formation of a third phase for a system containing a hydrophobic salts, whereas high temperature is advantageous that containing a hydrophilic one. From the observation on the composition of a third liquid phase, we consider that the SN2 reaction in the third liquid phase is not by quaternary ammonium ion pair, instead, is by the free anion. Therefore, we adopt a micelle-like mechanism to delineate the reaction in the third hquid phase. The reaction rate expression that derived is of a zero order form. Experiment result confirmed this kinetic model.