High Bromide Research Articles

Facile synthesis of A2mB2n-type starlike copolymers with two types of V-shaped arms by combination of RAFT, ATRP and ROP processes

Controlled synthesis of A2mB2n-type (m ≈ n ≈ 8) starlike copolymers comprising an oligomeric poly(styrene-co-maleimide) core and two types of V-shaped arms individually generated by ATRP and ROP was described. Multistep syntheses involving RAFT copolymerization, end group removal, ATRP of vinyl monomers such as styrene (St), methoxyethyl methacrylate (MEMA) and tert-butyl acrylate (tBA), and ROP of ε-caprolactone (CL) were used to construct the target miktoarm stars with controlled molecular weight and relatively low polydispersity (PDI = 1.07–1.22). The resultant star copolymers had high bromide functionality and uniform chain length of ATRP-generated arms, evident from chain extension polymerization and cleavage of arms. Meanwhile, a pH-responsive (PAA)2m(PCL)2n star was also obtained by selective hydrolysis. The synthetic strategy via combination of RAFT copolymerization and “core first” approach is versatile in constructing various A2mB2n stars, and this study further paves way for facile synthesis and properties of new types of miktoarm stars.

Peracetic acid oxidation of saline waters in the absence and presence of H ₂O ₂: secondary oxidant and disinfection byproduct formation.

Peracetic acid (PAA) is a disinfectant considered for use in ballast water treatment, but its chemical behavior in such systems (i.e., saline waters) is largely unknown. In this study, the reactivity of PAA with halide ions (chloride and bromide) to form secondary oxidants (HOCl, HOBr) was investigated. For the PAA-chloride and PAA-bromide reactions, second-order rate constants of (1.47 ± 0.58) × 10(-5) and 0.24 ± 0.02 M(-1) s(-1) were determined for the formation of HOCl or HOBr, respectively. Hydrogen peroxide (H2O2), which is always present in PAA solutions, reduced HOCl or HOBr to chloride or bromide, respectively. As a consequence, in PAA-treated solutions with [H2O2] > [PAA], the HOBr (HOCl) steady-state concentrations were low with a limited formation of brominated (chlorinated) disinfection byproducts (DBPs). HOI (formed from the PAA-iodide reaction) affected this process because it can react with H2O2 back to iodide. H2O2 is thus consumed in a catalytic cycle and leads to less efficient HOBr scavenging at even low iodide concentrations (<1 μM). In PAA-treated solutions with [H2O2] < [PAA] and high bromide levels, mostly brominated DBPs are formed. In synthetic water, bromate was formed from the oxidation of bromide. In natural brackish waters, bromoform (CHBr3), bromoacetic acid (MBAA), dibromoacetic acid (DBAA), and tribromoacetic acid (TBAA) formed at up to 260, 106, 230, and 89 μg/L, respectively for doses of 2 mM (ca. 150 mg/L) PAA and [H2O2] < [PAA]. The same brackish waters, treated with PAA with [H2O2] ≫ [PAA], similar to conditions found in commercial PAA solutions, resulted in no trihalomethanes and only low haloacetic acid concentrations.

Iodide, bromide, and ammonium in hydraulic fracturing and oil and gas wastewaters: environmental implications.

The expansion of unconventional shale gas and hydraulic fracturing has increased the volume of the oil and gas wastewater (OGW) generated in the U.S. Here we demonstrate that OGW from Marcellus and Fayetteville hydraulic fracturing flowback fluids and Appalachian conventional produced waters is characterized by high chloride, bromide, iodide (up to 56 mg/L), and ammonium (up to 420 mg/L). Br/Cl ratios were consistent for all Appalachian brines, which reflect an origin from a common parent brine, while the I/Cl and NH4/Cl ratios varied among brines from different geological formations, reflecting geogenic processes. There were no differences in halides and ammonium concentrations between OGW originating from hydraulic fracturing and conventional oil and gas operations. Analysis of discharged effluents from three brine treatment sites in Pennsylvania and a spill site in West Virginia show elevated levels of halides (iodide up to 28 mg/L) and ammonium (12 to 106 mg/L) that mimic the composition of OGW and mix conservatively in downstream surface waters. Bromide, iodide, and ammonium in surface waters can impact stream ecosystems and promote the formation of toxic brominated-, iodinated-, and nitrogen disinfection byproducts during chlorination at downstream drinking water treatment plants. Our findings indicate that discharge and accidental spills of OGW to waterways pose risks to both human health and the environment.

Wyniki badań hydrogeologicznych i objawów bitumiczności utworów paleozoicznych w otworze Goczałkowice IG 1(Górnośląskie Zagłębie Węglowe)

RESULTS OF A HYDROGEOLOGICAL STUDY OF PALEOZOIC ROCKS AND BITUMINOUS SYMPTOMS IN GOCZAŁKOWICE IG 1 BOREHOLE (UPPER SILESIAN COAL BASIN) Abstract. The Goczalkowice IG 1 borehole with the total depth of 3353.5 m has been drilled in the western part of the Carpathian Foredeep in the Upper Silesian Coal Basin. The aim of the drilling was to recognize the deep structure of the Upper Silesian depression and its hydrogeological environment as well as to verify the of hypothesis about the occurrence of hydrocarbon deposits in rocks of the Upper Carboniferous basement. The investigations of the rock matrix of the Lower Carboniferous, Devonian, Cambrian and Precambrian reservoir rocks showed generally its low open porosity (1.25% on average) and permeability (less than 0.1 mD on average). The formation waters in the Paleozoic deposits are highly mineralized thermal brines of Cl–Na–Ca hydrochemical type with a high iodide and bromide content. They are relict waters altered as a result of hydrogeological environment diagenesis. Direct investigations porformed in the borehole did not demonstrate free gas and oil occurrence in the reservoir rocks.

Formation and speciation of haloacetic acids in seawater desalination using chlorine dioxide as disinfectant

To evaluate the formation potential of disinfection byproducts (DBPs) in a SWRO system when chlorine dioxide (ClO2) is used as a chemical disinfectant, the impact of principle precursors such as natural organic matter (NOM) and bromide ion on haloacetic acids (HAAs) formation and its speciation was investigated. In the presence of high bromide levels found in seawater, the active oxidizing agents formed by the action of ClO2 can react with NOM, resulting in halogenation reactions, and the production of brominated DBPs as the predominant byproducts. Elevating the initial levels of organic substances and bromide ions not only enhanced the total content of HAA5 formed, but also shifted the speciation of HAAs from the chlorinated to fully brominated forms at higher disinfectant doses and longer contact times of ClO2 disinfection. In addition, HAA5 formation potential increased in the order of transphilic>hydrophobic>hydrophilic NOM, suggesting HAA5 yield formed during ClO2 disinfection significantly depends on the characteristics of NOM that can lead to different speciation distribution of DBPs. However, at high doses of ClO2, it was observed that the disinfectant dose plays a more important role in speciation distribution of HAA5 than the characteristics of organic precursors.

Terminally Haloalkene Compounds(New Products) | High Purity Alkyl Bromides

RETURN TO ISSUEPREVAdvertisementNEXTTerminally Haloalkene Compounds(New Products) | High Purity Alkyl BromidesCite this: Chem. Eng. News 2014, 92, 46, 31Publication Date (Print):November 17, 2014Publication History Published online31 March 2015Published inissue 17 November 2014https://doi.org/10.1021/cen-09246-ad19Copyright © 2014 Chemical & Engineering NewsArticle Views63Altmetric-Citations-LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (603 KB) SUBJECTS:Alkyls,Anions Get e-Alerts

Enhanced formation of disinfection byproducts in shale gas wastewater-impacted drinking water supplies.

The disposal and leaks of hydraulic fracturing wastewater (HFW) to the environment pose human health risks. Since HFW is typically characterized by elevated salinity, concerns have been raised whether the high bromide and iodide in HFW may promote the formation of disinfection byproducts (DBPs) and alter their speciation to more toxic brominated and iodinated analogues. This study evaluated the minimum volume percentage of two Marcellus Shale and one Fayetteville Shale HFWs diluted by fresh water collected from the Ohio and Allegheny Rivers that would generate and/or alter the formation and speciation of DBPs following chlorination, chloramination, and ozonation treatments of the blended solutions. During chlorination, dilutions as low as 0.01% HFW altered the speciation toward formation of brominated and iodinated trihalomethanes (THMs) and brominated haloacetonitriles (HANs), and dilutions as low as 0.03% increased the overall formation of both compound classes. The increase in bromide concentration associated with 0.01-0.03% contribution of Marcellus HFW (a range of 70-200 μg/L for HFW with bromide = 600 mg/L) mimics the increased bromide levels observed in western Pennsylvanian surface waters following the Marcellus Shale gas production boom. Chloramination reduced HAN and regulated THM formation; however, iodinated trihalomethane formation was observed at lower pH. For municipal wastewater-impacted river water, the presence of 0.1% HFW increased the formation of N-nitrosodimethylamine (NDMA) during chloramination, particularly for the high iodide (54 ppm) Fayetteville Shale HFW. Finally, ozonation of 0.01-0.03% HFW-impacted river water resulted in significant increases in bromate formation. The results suggest that total elimination of HFW discharge and/or installation of halide-specific removal techniques in centralized brine treatment facilities may be a better strategy to mitigate impacts on downstream drinking water treatment plants than altering disinfection strategies. The potential formation of multiple DBPs in drinking water utilities in areas of shale gas development requires comprehensive monitoring plans beyond the common regulated DBPs.

정수처리에서 염소 처리시 요오드계 트리할로메탄류 생성에 영향을 미치는 인자들

Effects of bromide (Br) and iodide (I) concentrations, chlorine (Cl2) doses, pH, temperature, ammonia nitrogen concentrations, reaction times and water characteristics on formation of iodinated trihalomethanes (I-THMs) during oxidation of iodide containing water with chlorine were investigated in this study. Results showed that the yields of I-THMs increased with the high bromide and iodide level during chlorination. The elevated pH significantly increased the yields of I-THMs during chlorination. The formation of I-THMs was higher at 20°C than 4°C, 10°C and 30°C. In chloramination study, addition of ammonium chloride (NH4Cl) markedly increased the formation of I-THMs. Among the water samples collected from seven water sources including wastewater treatment plant (WWTP) effluent water (EfOM water), prepared humic containing water (HA water) and algal organic matter (AOM) containing water (AOM water), EfOM water generated the highest yields of I-THMs (12.31 μg/mg DOC), followed by HA water (4.96 μg/mg DOC), while AOM water produced the lowest yields of I-THMs (0.99 μg/mg DOC). SUVA254 values of EfOM water , HA water and AOM water were 1.38 L/mg・m, 4.96 L/mg·m and 0.97 L/mg·m, respectively. The I-THMs yields had a low correlation with SUVA254 values (r = 0.002).

Measurement of radionuclide activities induced in target components of an IBA CYCLONE 18/9 by gamma-ray spectrometry with HPGe and LaBr3: Ce detectors.

Cyclotrons are used worldwide to produce radiopharmaceuticals by proton irradiation of a suitable target. The intense secondary neutron beam generated by proton interactions with the target induce high radionuclide activities in the target assembly parts that may result in an exposure to high dose levels of the operators during maintenance. The main goal of this work is to evaluate gamma-emitting radionuclide activities induced in Havar foils and titanium windows of a target assembly and carousel stripper forks of an IBA CYCLONE 18/9 cyclotron. The knowledge of radionuclide inventory for each component is required by many companies to assess risk for operators before waste handling and disposal. Gamma-ray spectrometric analyses were carried out with High Purity Germanium (HPGe) and Lanthanum bromide (LaBr3:Ce) scintillation detectors. HPGe is the most used detector for its high energy resolution although it is more suitable for use in a laboratory. The use of LaBr3:Ce can be considered a viable option, particularly in realizing a portable spectrometric system to perform "on-site" measurements and a fast dose rate evaluation before the disposal of activated parts. Due to a high activity of target assembly components replaced after a typical irradiation cycle (about 5000 μAh integrated beam current), gamma-ray spectrometric measurements were performed at a large distance from the detector, even more than 100 cm, or by using a purposely realized Lead-walled collimator. The identification of some key-radionuclides allows to evaluate through simple formulations the dose rate behavior for each component as function of decay time from the last irradiation. The knowledge of the dose rate behavior is a significant piece of information to health physicists for waste handling with safety at work. For an Havar™ foil, the dose rate will be reduced to about 1/1,000 of the starting value after a decay period of approximately 4 y (about 1,500 d), with a relatively safety at product disposal work. For a longer time, only long-lived radionuclides (57)Co, (60)Co, and (54)Mn contribute to dose rate.

SU‐E‐J‐121: Measuring Prompt Gamma Emission Profiles with a Multi‐Stage Compton Camera During Proton Beam Irradiaition: Initial Studies

Purpose:Recent studies have suggested that the characteristics of prompt gammas (PG) emitted during proton beam irradiation are advantageous for determining beam range during treatment delivery. The purpose of this work was to determine the feasibility of determining the proton beam range from PG data measured with a prototype Compton camera (CC) during proton beam irradiation.Methods:Using a prototype multi‐stage CC the PG emission from a water phantom was measured during irradiation with clinical proton therapy beams. The measured PG emission data was used to reconstruct an image of the PG emission using a backprojection reconstruction algorithm. One dimensional (1D) profiles extracted from the PG images were compared to: 1) PG emission data measured at fixed depths using collimated high purity Germanium and Lanthanum Bromide detectors, and 2) the measured depth dose profiles of the proton beams.Results:Comparisons showed that the PG emission profiles reconstructed from CC measurements agreed very well with the measurements of PG emission as a function of depth made with the collimated detectors. The distal falloff of the measured PG profile was between 1 mm to 4 mm proximal to the distal edge of the Bragg peak for proton beam ranges from 4 cm to 16 cm in water. Doses of at least 5 Gy were needed for the CC to measure sufficient data to image the PG profile and localize the distal PG falloff.Conclusion:Initial tests of a prototype CC for imaging PG emission during proton beam irradiation indicated that measurement and reconstruction of the PG profile was possible. However, due to limitations of the operational parameters (energy range and count rate) of the current CC prototype, doses of greater than a typical treatment dose (∼2 Gy) were needed to measure adequate PG signal to reconstruct viable images.Funding support for this project provided by a grant from DoD.

Identification of vibration characteristics in infrared spectrum of polybrominated diphenyl ethers congeners based on Br substituents

Structure optimization and frequency calculations of 209 kinds of PBDEs homologues were carried out at the B3LYP/6-31G(d) level based on density functional theory, the known experimental parameters of 4 PBDEs congeners were compared with the calculated values, and the average analog coefficient was 0. 989. The main vibration of DE and BDE-209 which contained only H atoms or Br substituent in the benzene ring was assigned due to their less interference for various infrared spectrum vibrations. C-Br bond vibration which was often coupled with other forms of vibration was not easy to distinguish between PBDEs congeners. With the characteristics of universality, strong vibration and identifiable, triangular breathing vibration of the benzene rings in the infrared spectrum was selected as a characteristic vibration among different PBDEs homologues, the analysis results showed that the ortho-substituted and para-substituted Br could significantly improve the vibration frequency of triangular breathing vibration, while the meta-substituted Br played the opposite role; For the low bromide, the more the substituents in ortho position, the higher the frequency, while for the high bromide homologues, simultaneous existence in ortho-position and para-position would have a higher frequency; With the same substituted location, the more the substituent in the same benzene ring, the higher the vibration frequency. SVM regression model was used to verify the relative relationship between Br substituent and triangle breathing vibration frequency of the benzene rings, and the simulation efficiency coefficient of model was 0. 956. The study provided a theoretical basis and guidance for actually testing and identifying PBDEs homologues in the environment.

Polymerized ionic liquid diblock copolymers with long alkyl side-chain length

A polymerized ionic liquid (PIL) diblock copolymer with a long alkyl side-chain, poly(MMA-b-MUBIm-Br), was synthesized at various compositions from an ionic liquid monomer, (1-[(2-methacryloyloxy)undecyl]-3-butylimidazolium bromide) (MUBIm-Br), and a non-ionic monomer, methyl methacrylate (MMA). The PIL diblock copolymer was synthesized via post-functionalization from its non-ionic precursor PIL diblock copolymer, poly(MMA-b-BrUMA) (BrUMA = 11-bromoundecyl methacrylate), which was synthesized via the reverse addition fragmentation chain transfer (RAFT) polymerization technique. Differential scanning calorimetry reveals two distinct constant glass transition temperatures (Tgs) with a low PIL segment Tg. These PIL block copolymers result in easily processable, flexible, transparent films with high mechanical strength. A high bromide ion conductivity of 64.85 mS cm−1 at 80 °C and 90% RH was measured for the PIL diblock copolymer with an ion exchange capacity (IEC) of 1.44 meq/g (23.3 mol% MUBIm-Br). Interestingly, this result was three times higher than its analogous PIL homopolymer (2.75 meq/g; 100 mol% MUBIm-Br) and an order of magnitude higher than a PIL block copolymer from a previous study with similar chemistry, similar IEC, higher water content, but shorter alkyl side-chain length. Ion conductivity did not scale as expected with water content, which is unusual for water-assisted ion transport (e.g., protons, hydroxide, chloride) in ion-containing polymers, and therefore suggests other mechanisms that impact ion transport in PIL block copolymers.

Addition of hydrogen peroxide for the simultaneous control of bromate and odor during advanced drinking water treatment using ozone

Complete removal of the characteristic septic/swampy odor from Huangpu River source water could only be achieved under an ozone dose as high as 4.0 mg/L in an ozone-biological activated carbon (O3-BAC) process, which would lead to the production of high concentrations of carcinogenic bromate due to the high bromide content. This study investigated the possibility of simultaneous control of bromate and the septic/swampy odor by adding H2O2 prior to the O3-BAC process for the treatment of Huangpu River water. H2O2 addition could reduce the bromate concentration effectively at an H2O2/O3 (g/g) ratio of 0.5 or higher. At the same time, the septic/swampy odor removal was enhanced by the addition of H2O2, although optimization of the H2O2/O3 ratio was required for each ozone dose. At an ozone dose of 2.0 mg/L, the odor was removed completely at an H2O2/O3 ratio of 0.5. The results indicated that H2O2 application at a suitable dose could enhance the removal of the septic/swampy odor while suppressing the formation of bromate during ozonation of Huangpu River source water.

Kinetics of Bromochloramine Formation and Decomposition

Batch experiments were performed to study the kinetics of bromochloramine formation and decomposition from the reaction of monochloramine and bromide ion. The effects of pH, initial monochloramine and bromide ion concentrations, phosphate buffer concentration, and excess ammonia were evaluated. Results showed that the monochloramine decay rate increased with decreasing pH and increasing bromide ion concentration, and the concentration of bromochloramine increased to a maximum before decreasing gradually. The maximum bromochloramine concentration reached was found to decrease with increasing phosphate and ammonia concentrations. Previous models in the literature were not able to capture the decay of bromochloramine, and therefore we proposed an extended model consisting of reactions for monochloramine autodecomposition, the decay of bromamines in the presence of bromide, bromochloramine formation, and bromochloramine decomposition. Reaction rate constants were obtained through least-squares fitting to 11 data sets representing the effect of pH, bromide, monochloramine, phosphate, and excess ammonia. The reaction rate constants were then used to predict monochloramine and bromochloramine concentration profiles for all experimental conditions tested. In general, the modeled lines were found to provide good agreement with the experimental data under most conditions tested, with deviations occurring at low pH and high bromide concentrations.

Kinetic Investigations of p-Xylene Oxidation to Terephthalic Acid with a Co/Mn/Br Catalyst in a Homogeneous Liquid Phase

Kinetic investigations of the liquid phase oxidation of p-xylene (pX) to terephthalic acid (TPA) with Co/Mn/Br catalyst were performed in a stirred 50 mL Parr reactor at 200 °C and 15 bar pressure under conditions wherein product precipitation is avoided. The oxidant (O2) was introduced by sparging into the liquid phase at constant gas-phase O2 partial pressure. Apparent kinetic rate constants, estimated by regressing experimental conversion data to a pseudo-first order lumped kinetic model, are at least an order of magnitude greater than those reported in the literature for similar catalytic reactions. We attribute this difference to the presence of gas–solid and liquid–solid mass transfer resistances in the previous studies wherein the TPA product precipitates as it forms, trapping intermediate products and slowing down their oxidation rates. Our results also indicate that it is not possible to completely eliminate the gas–liquid mass transfer limitations associated with the fast intermediate oxidation steps, even when operating without solids formation and at high stirrer speeds. Other types of reactor configurations are therefore needed to better overcome gas–liquid mass transfer limitations. Systematic studies of bromide concentration effects show that the observed reaction rates become zero order in bromide concentration at sufficiently high bromide levels where the elimination of intermediate 4-(bromomethyl)benzoic acid by oxidation is favored. Further, the rate constants do not show any statistically significant dependence on pX concentration as suggested in other reports involving the traditional three-phase gas–liquid–solid reaction system. This again confirms that the formation of a solid phase hinders the overall oxidation rate, resulting in much smaller apparent rate constants.

Examining the interrelationship between DOC, bromide and chlorine dose on DBP formation in drinking water — A case study

During drinking water treatment aqueous chlorine and bromine compete to react with natural organic matter (NOM). Among the products of these reactions are potentially harmful halogenated disinfection by-products, notably four trihalomethanes (THM4) and nine haloacetic acids (HAAs). Previous research has concentrated on the role of bromide in chlorination reactions under conditions of a given NOM type and/or concentration. In this study different concentrations of dissolved organic carbon (DOC) from U.K. lowland water were reacted with varying amounts of bromide and chlorine in order to examine the interrelationship between the three reactants in the formation of THM4, dihaloacetic acids (DHAAs) and trihaloacetic acids (THAAs). Results showed that, in general, molar yields of THM4 increased with DOC, bromide and chlorine concentrations, although yields did fluctuate versus chlorine dose. In contrast both DHAA and THAA yields were mainly independent of changes in bromide and chlorine dose at low DOC (1mg·L−1), but increased with chlorine dose at higher DOC concentrations (4mg·L−1). Bromine substitution factors reached maxima of 0.80, 0.67 and 0.65 for the THM4, DHAAs and THAAs, respectively, at the highest bromide/chlorine ratio studied. These results suggest that THM4 formation kinetics depend on both oxidation and halogenation steps, whereas for DHAAs and THAAs oxidation steps are more important. Furthermore, they indicate that high bromide waters may prove more problematic for water utilities with respect to THM4 formation than for THAAs or DHAAs. While mass concentrations of all three groups increased in response to increased bromide incorporation, only the THMs also showed an increase in molar yield. Overall, the formation behaviour of DHAA and THAA was more similar than that of THM4 and THAA.

High Purity Alkyl Bromides by Isomer Control Technology

RETURN TO ISSUEPREVAdvertisementNEXTHigh Purity Alkyl Bromides by Isomer Control TechnologyCite this: Chem. Eng. News 2013, 91, 40, 52Publication Date (Print):October 7, 2013Publication History Published online31 March 2014Published inissue 7 October 2013https://doi.org/10.1021/cen-09140-ad40Copyright © 2013 Chemical & Engineering NewsArticle Views59Altmetric-Citations-LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (89 KB) SUBJECTS:Anions,Molecular structure,Alkyls Get e-Alerts

Electrostatically controlled nematic and smectic assembly of gold nanorods

The assembly of gold nanorods(GNRs) into different liquid crystalline structures can be controlled by tuning their surface electric potential. After mildly removing excess surfactants in the GNRs solution, the electrostatic interaction between GNRs can be tuned by adjusting counter ion concentration. Specifically, nematic and smectic structures formed after solvent evaporation at low and high bromide concentrations, respectively. These results could be helpful for fabricating anisotropy enabled devices composed of metal and semiconductor nanorods.

High Purity Alkyl Bromides by Isomer Control Technology

High Purity Alkyl Bromides by Isomer Control Technology

A Stable Bacterial Peroxidase with Novel Halogenating Activity and an Autocatalytically Linked Heme Prosthetic Group

Reconstructing the phylogenetic relationships of the main evolutionary lines of the mammalian peroxidases lactoperoxidase and myeloperoxidase revealed the presence of novel bacterial heme peroxidase subfamilies. Here, for the first time, an ancestral bacterial heme peroxidase is shown to possess a very high bromide oxidation activity (besides conventional peroxidase activity). The recombinant protein allowed monitoring of the autocatalytic peroxide-driven formation of covalent heme to protein bonds. Thereby, the high spin ferric rhombic heme spectrum became similar to lactoperoxidase, the standard reduction potential of the Fe(III)/Fe(II) couple shifted to more positive values (-145 ± 10 mV at pH 7), and the conformational and thermal stability of the protein increased significantly. We discuss structure-function relationships of this new peroxidase in relation to its mammalian counterparts and ask for its putative physiological role.