Bromide Solution Research Articles

Selective Voltammetric Sensor for the Simultaneous Quantification of Tartrazine and Brilliant Blue FCF.

Tartrazine and brilliant blue FCF are synthetic dyes used in the food, cosmetic and pharmaceutical industries. The individual and/or simultaneous control of their concentrations is required due to dose-dependent negative health effects. Therefore, the paper presents experimental results related to the development of a sensing platform for the electrochemical detection of tartrazine and brilliant blue FCF based on a glassy carbon electrode (GCE) modified with MnO2 nanorods, using anodic differential pulse voltammetry. Homogeneous and stable suspensions of MnO2 nanorods have been obtained involving cetylpyridinium bromide solution as a cationic surfactant. The MnO2 nanorods-modified electrode showed a 7.9-fold increase in the electroactive surface area and a 72-fold decrease in the electron transfer resistance. The developed sensor allowed the simultaneous quantification of dyes for two linear domains: in the ranges of 0.10-2.5 and 2.5-15 μM for tartrazine and 0.25-2.5 and 2.5-15 μM for brilliant blue FCF with detection limits of 43 and 41 nM, respectively. High selectivity of the sensor response in the presence of typical interference agents (inorganic ions, saccharides, ascorbic and sorbic acids), other food dyes (riboflavin, indigo carmine, and sunset yellow), and vanillin has been achieved. The sensor has been tested by analyzing soft and isotonic sports drinks and the determined concentrations were close to those obtained involving the chromatography technique.

Modulation of plasmonic chiral shell growth on gold nanorods via nonchiral surfactants.

Recently, in combination with seed-mediated growth, thiolated chiral molecule-guided growth has shown great promise in obtaining chiral plasmonic nanostructures. Previously, with the assistance of chiral cysteines (Cys), we realized helical growth of plasmonic shells on gold nanorod (AuNR) seeds dispersed in cetyltrimethylammonium bromide (CTAB) solution. Herein, we further studied the roles of non-chiral cationic surfactants in tuning the helical growth. Both the counter anion and the hydrocarbon chain length of the surfactants were found to affect the formation of helical shells greatly. In particular, we exhibited surfactant-modulated conversion of the chiral shell deposition mode between layer growth and island growth. By optimizing growth conditions, an obvious plasmonic circular dichroism (PCD) response could be achieved for the island helical shell. Our findings demonstrated promising potential of nanochemical synthesis in fabricating chiral plasmonic nanostructures with small structural sizes.

Процессы «turnover» в реакциях разложения ацилсодержащих субстратов в организованных микрогетерогенных системах

Design of organized microheterogeneous systems for fast disrupting (disintegration) of acylcontaining substrates (including organophosphorus compounds) is based on the use of highly reactive compounds. Reagents (catalysts) ability to provide “turnover” is of great impotence. Kinetic regularities for 4- nitrophenylacetate (PNPA) deacylation with 1-methyl-3-(2-hydroximinoethyl)-imidazolium chloride (oxime), chloral, and their mixtures were studied in water and cetyltrimethylammonium bromide (CTAB) solutions, under pH = const and [CTAB] = 10-2 M. Rate constants dependences upon nucleophile (catalyst) and detergent concentration are typical for reactions in water and micellar pseudophase. Transferring of PNPA deacylation from water into surfactant micelles leads to three orders rate enhancement. Kinetic experiments at different substrate concentrations indicate that a) first order rate constant in the chloral-CTAB system does not change up to tenfold excess of PNPA; b) first order rate constant in the oxime-CTAB system decreases for approx. 40% at PNPA excess; c) all advantages of “turnover” are achievable in the system chloral-oximeCTAB, where chloral provides first disintegration of acylated oxime with generation of highly reactive oximate-ion. Results obtained pave the way to modifying organized microheterogeneous systems, first of all, by surfactant structure changes.

Adsorption of Glyphosate by Palygorskite

Glyphosate affects ecosystems due to exposure of non-target crops and is a persistent contaminant at low concentrations. The application of palygorskite to reduce glyphosate contamination in Brazil is an environmentally friendly way to remediate impacted areas. This research evaluated palygorskite application for glyphosate adsorption present in a synthetic effluent. Palygorskite samples were ore dressed by wet granulometric classification and wet magnetic separation and submitted to organophilization with cetyltrimethyl ammonium bromide solutions at concentrations of 0.01, 0.1, 1.0 and 1.5% (w/w), and the organo-palygorskite was applied in glyphosate adsorption tests. After ore dressing there was an increase in its cation exchange capacity from 19 to 41 meq 100 g-1 and the surface area was 149 g m-2. The 1.0% organo-palygorskite adsorbed about 86% of glyphosate from synthetic aqueous effluent. Based on this high adsorption yield, the organo-palygorskite is a potential adsorbent for remediation of effluents containing the toxic herbicide glyphosate.

Viscosity Correlation for Aqueous Lithium Bromide Solution

A correlation for dynamic viscosity of aqueous lithium bromide solution is proposed. The correlation is based on an empirical approach accounting for physical limitations. The data are compiled from 11 sources over a temperature range from − 20 ^{circ }C to 110 ^{circ }C and from pure water to salt mass fractions of 65 %. The correlation succeeds in predicting the solution’s viscosity over the chosen range of measured data. In most parts of its validity range the accuracy is significantly improved compared to previous equations.

Fitness recovery and two-generation phenotypic plasticity in the freshwater snail Planorbarius corneus L. exposed to hyperosmotic solutions

Background and purpose: Hyperosmotic solutions of calcium chloride and calcium bromide, extensively used in the oil industry, can be a source of aquatic pollution.Materials and methods: In the present study, we investigated whether the freshwater snail Planorbarius corneus L., previously chronically exposed to toxic concentrations of these chemicals, can recover fecundity and growth in clean water. We also examined if a higher tolerance could be induced in F1 offspring after parental and developmental chronic exposure to the chemicals.Results: The fitness-recovery study showed a high compensatory potential of the snails to recover fitness through increased reproduction and growth. In the tolerance study, we observed increased tolerance in F1 offspring in hyperosmotic solutions of calcium chloride. However, there was no significant improvement of reproduction performance in bromide-containing solutions.Conclusions: Increased tolerance was associated with a redirection of resources from growth to maintenance and survival.

Transformation of Corn Stover into Furan Aldehydes by One-Pot Reaction with Acidic Lithium Bromide Solution

Currently, the production of furan aldehydes from raw biomass suffers from low furfural yield and high energy consumption. In this study, a recyclable and practical method was explored for the preparation of furfural from corn stover by the one-pot reaction by acidic lithium bromide solution (ALBS) without pretreatment and enzymolysis. In the ALBS reaction, the furan aldehydes were generated by the degradation of lignocellulose; however, the products were unstable and were further dehydrated to form humins. So, dehydration reaction was inhibited in this study, and the high yield of furan aldehydes was obtained, in which 2.94 g/L of furfural and 2.78 g/L of 5-hydroxymethyl furfural (5-HMF) were generated with high solid loading (10 wt%), the presence of commercial catalyst ZSM-5 and co-solvent tetrahydrofuran (THF) at 140 °C for 200 min. Via this method, almost 100% of hemicellulose was transformed to furfural, and 40.71% of cellulose was transformed to 5-HMF, which was based on the theoretical yield of HMF (8.35 g) from glucose (29.30 g) produced from cellulose. After the reaction, the catalyst ZSM-5 was the main component in the solid residue and kept a suitable performance. THF azeotrope was easily separated from the slurry by evaporation. During the removal of THF, lignin was precipitated from the liquid phase and showed lower molecular weight and abundant active groups, which was a potential feedstock for producing valuable aromatics and polymers. Thus, in a one-pot reaction, the ideal yield of furan aldehydes from raw biomass was obtained on a lab scale, and the catalyst, THF, and LiBr were easily recycled, which provided an option to realize the economical production of sustainable furan aldehydes from raw biomass.

Dielectric Relaxation of Ion-pairs, Micelles and Hydration in Aqueous Hexyltrimethylammonium Bromide Solutions

Through dielectric measurements of aqueous n-hexyltrimethylammonium bromide solutions, the structure and dynamics of ion-pairs, micelles, and water are investigated as functions of concentration and temperature. The frequency range of the study was ∼ 0.2 ≤ν/GHz ≤ 89, and the concentrations were changed from 0.0448 to 0.8476 mol.dm−3 at 298.15 K. The effects of temperature (278.15 ≤ T/K ≤ 338.15) on two selected solutions with concentrations above and below the critical micelle concentration were examined. A summation of three Debye processes fits the complex permittivity data of solutions with concentrations below the critical micelle concentration. To fit the spectra above the critical micelle concentration, a summation of five Debye processes is needed. Below the critical micelle concentration, solutes relax due to the tumbling motion of solvent-shared ion pairs. The two micelle relaxation processes that have been seen are the result of free and bound counter ions tangentially and radially diffusing around the charged micelles. Maxwell-Wagner relaxation is equivalent to the high frequency micelle relaxation process. Both the solvent and micelle dispersion provide acceptable volume fractions. Hexyltrimethylammonium behaves like higher n-alkyltrimethylammonium micelles in the context of micelle relaxation. Before critical micelle concentration, the cations, anions, and ion pairs strongly hydrate a total of ∼18 ± 4 non-rotational water molecules. Beyond the critical micelle concentration, there are an additional ∼ 5 ± 2 non-rotational water molecules in addition to ∼ 15 ± 3 slower-moving water molecules in the hydrophobic hydration shell.

Direct Resolution of the Interactions of a Hydrocarbon Gas with Adsorbed Surfactant Monolayers at the Water/Air Interface Using Neutron Reflectometry

We have directly resolved in the present work the interfacial composition during and after the interactions of a saturated atmosphere of oil vapor with soluble surfactant solutions at a planar water/air interface for the first time. Experiments were conducted on interactions of hexane vapor with solutions of alkyltrimethylammonium bromides and sodium dodecyl sulfate to observe the balance between cooperativity and competition of the components at the interface. In all cases, hexane adsorption was strongly enhanced by the presence of the surfactant, even at bulk surfactant concentrations four orders of magnitude below the critical micelle concentration. Cooperativity of the surfactant adsorption was observed only for sodium dodecyl sulfate at intermediate bulk concentrations, yet for all four systems, competition set in at higher concentrations, as hexane adsorption reduced the surfactant surface excess. The data fully supported the complete removal of hexane from the interface following venting of the system to remove the saturated atmosphere of oil vapor. These results help to identify future experiments that would elaborate and could explain the cooperativity of surfactant adsorption, such as on cationic surfactants with short alkyl chains and a broader series of anionic surfactants. This work holds relevance for oil recovery applications with foam, where there is a gas phase saturated with oil vapor.

Photophysical properties and aggregation behavior of diethylene glycol substituted pyropheophorbide-a in cationic surfactant solutions

The aggregation behavior of a novel amphiphilic photosensitizer - pyropheophorbide-[Formula: see text] 17-diethylene glycol ester 1 was studied in aqueous and aqueous-organic mixtures by means of steady-state absorption and fluorescence emission spectroscopy. The formation of [Formula: see text]-aggregates with a bathochromic shift of the absorption bands, weak fluorescence and resonance enhancement of the light scattering was observed in the mixed water-organic solvents. Solubilization studies in micellar cationic surfactant solutions of alkyl trimethylammonium bromides (C[Formula: see text]TAB) and alkyl triphenylphosphonium bromides (C[Formula: see text]TPPB) resulted in the most effective stabilization of the fluorescent monomolecular form of 1 in C[Formula: see text]TPPB micelles. It was shown that [Formula: see text]-aggregate formation in submicellar surfactant solutions is the initial stage of the solubilization process, which significantly increases in phosphate buffer medium at pH 7.4. Fluorescence lifetime ([Formula: see text] of 1 in DMSO was found to be 7.4 ns, fluorescence quantum yield - 34% and singlet oxygen quantum yield - 62%. The results obtained indicate the need for further studies of compound 1 solubilized in C[Formula: see text]TPPB micelles as the most promising prototype of the drug formulation for mitochondria-targeted photodynamic therapy of cancer.

Knockdown of DAPK1 attenuates IL-1β-induced extracellular matrix degradation and inflammatory response in osteoarthritis chondrocytes via regulating the p38 MAPK-signaling pathway.

To reveal the possible effects of death-associated protein kinase 1 (DAPK1) on the progression of osteoarthritis (OA) and the potential underlying mechanism. : The expression of DAPK1 in OA and normal samples and interleukin (IL)-1β-stimulated chondrocytes was analyzed by quantitative real-time polymerase chain reaction and Immunoblot assay. Cell viability, proliferation, and apoptosis in DAPK1-knockdown cells stimulated with IL-1β were detected by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) solution, 5-ethynyl-2β-deoxyuridine staining and flow cytometry. The chondrocyte degradation and inflammatory response in IL-1β-induced chondrocytes were investigated by Immunoblot analysis and enzyme-linked-immunosorbent serologic assay. In addition, the effect of DAPK1 on p38 mitogen-activated protein kinase (MAPK) activation was analyzed by immunoblot assay. : This study revealed that DAPK1 was highly expressed in OA patients and IL-1β-induced chondrocytes. Down-regulation of DAPK1 enhanced IL-1β-induced chondrocyte proliferation. DAPK1 knockdown inhibited IL-1β-induced chondrocyte degradation. In addition, DAPK1 depletion inhibited IL-1β-induced chondrocyte inflammation. Mechanically, it was revealed that down--regulation of DAPK1 could inhibit the p38 MAPK pathway, and therefore affected progression of OA. : DAPK1 knockdown attenuates IL-1β-induced extracellular matrix degradation and inflammatory response in OA chondrocytes by regulating the p38 MAPK pathway.

Effect of structure and operation parameters on heat and mass transfer coefficients of single‐bubble absorption for lithium bromide solution

Bubble absorption has an efficient performance in absorption units, and lithium bromide (LiBr)-H2O is the most popular working medium in absorption system due to its safety and environmental protection. Limited to the vacuum operation, the researches of bubble absorption for LiBr solution are less reported and the bubble absorption characteristic for LiBr solution is still not clear. In this study, a single-bubble heat and mass transfer model is established to investigate the heat and mass transfer coefficients of bubble absorption for LiBr solution under vacuum condition. A visible experimental platform is established to validate the feasibility of vacuum operation and the model accuracy. The experimental results showed the relative deviation is less than 11.9%. Base on the current model, the effects of structure and operation parameters are comprehensively analyzed to explore the appropriate configuration. The results indicate that the heat and mass transfer coefficients increase significantly with the increase of the orifice diameter and the bubble velocity, while they reduce with the increase of solution concentration. It can be explained that large orifice diameter expands the contact area, and high velocity strengthens the convection, which promote the absorption. Dilute solution concentration reduces the viscous force and surface tension, thereby enhancing the heat transfer. It is expected to provide guidance for the heat and mass transfer mechanisms and contribute to advance the structure and configuration of absorption system.

Hydrothermal Modification of TS-1 Zeolites with Organic Amines and Salts to Construct Highly Selective Catalysts for Cyclopentene Epoxidation

Developing efficient heterogeneous catalysts for cyclic olefins epoxidation is highly attractive for meeting the growing need for various cyclic epoxides. Herein, hierarchical TS-1 zeolite with relatively abundant mesopores and less amount of surface hydroxyl groups was obtained by hydrothermal modification of an as-synthesized TS-1 zeolite with a mixed solution of ammonia, tetrapropylammonium bromide (TPABr) and KCl. The post-modified TS-1 zeolite exhibited much higher catalytic activity (52% conversion) and epoxide selectivity (98%) for the epoxidation of cyclopentene than the conventional TS-1 zeolites. The excellent catalytic activity of the hierarchical TS-1 could be mainly assigned to the enhancement of the mass transport ability and the accessibility of the active Ti species, while the improvement of epoxidation selectivity may be mainly related to the introduction of a certain amount of K+ that can effectively modulate the coordination environment of Ti species as well as the polarity of the zeolite. This work demonstrated that a highly active and selective catalyst for the H2O2-mediated cyclopentene epoxidation could be obtained by concurrently generating mesopore and extinguishing the unfavorable defective hydroxyl groups through the simple hydrothermal treatment of the conventional TS-1 zeolite with a mixed base/salt solution.

Hydrolytic reactivity of novel copper(II) complexes with reduced N-salicylate threonine Schiff bases: distinguishable effects of various micelles

Three new bi- or tetranuclear copper (II) complexes (complexes 1, 2 and 3) with reduced N-salicylate threonine were synthesized and characterized by single crystal X-ray diffraction, X-ray powder diffraction, UV–vis, and thermogravimetric analysis. Single-crystal diffraction analysis reveals that these complexes have similar coordination modes and conformations which were linked into multidimensional networks through some weak interactions. These three complexes were employed to promote the hydrolytic cleavage of p-nitrophenyl picolinate (PNPP) and p-nitrophenyl acetate (PNPA). Catalytic reactivities of the as-prepared complexes show that in the hydrolysis of p-nitrophenyl acetate (PNPA) these three complexes provide 51, 45, 39-fold rate acceleration as compared to spontaneous hydrolysis of PNPA at pH 7.0, respectively. Under selected conditions, excess three orders of magnitude rate enhancement were observed for the catalytic hydrolysis of another carboxylic ester, p-nitrophenyl picolinate (PNPP). Furthermore, these complexes efficiently promote the PNPA hydrolysis in micellar solution of cetyltrimethylammonium bromide (CTAB) or bis(hexadecylhexmethyl ammonium)ethane bromide (16−6−16) giving rise to excess two orders of magnitude rate enhancement which is approximate 2.0 − 4.0 times higher than that in the buffer. However, the introduction of micelles of n-lauroylsarcosine sodium (LSS) or double-chained C22/8 surfactant did not increase the rate or even inhibited the hydrolysis reaction in contrast with buffered aqueous medium.

Self-Assembly and Micellar Transition in CTAB Solutions Triggered by 1-Octanol.

This study exploits higher-order micellar transition ranging from ellipsoidal to rodlike to wormlike induced by 1-octanol (C8OH) in an aqueous solution of cetyltrimethylammonium bromide (CTAB), characterizing phase behavior, rheology, and small-angle neutron scattering (SANS). The phase diagram for the ternary system CTAB-C8OH-water was constructed, which depicted the varied solution behavior. Such performance was further inferred from the rheology study (oscillatory-shear frequency sweep (ω) and viscosity (η)) that displayed an interesting solution behavior of CTAB solutions as a function of C8OH. It was observed that at low C8OH concentrations, the solutions appeared viscous/viscoelastic fluids that changed to an elastic gel with an infinite relaxation time at higher concentrations of C8OH, thereby confirming the existence of distinct micelle morphologies. Small-angle neutron scattering (SANS) provided various micellar parameters such as aggregation numbers (Nagg) and micellar size/shape. The experimental results were further validated with a computational simulation approach. The molecular dynamic (MD) study offered an insight into the molecular interactions and aggregation behavior through different analyses, including radial distribution function (RDF), radius of gyration (Rg), and solvent-accessible surface area (SASA).

The attraction between like-charged oil-in-water emulsion droplets induced by ionic micelles

Although extensive work has been reported that micelles can induce depletion attraction between two solid spheres or a sphere and a plate, the effect of different micelles on the depletion between two soft surfaces has been rarely reported. Optical tweezers were used to measure the forces between two oil-in-water emulsions in solutions of sodium dodecylbenzenesulfonate (SDBS), cetyltrimethylammonium bromide (CTAB), and octylphenol polyoxyethylene ether with ten oxyethylene glycol ether (OP-10) at varying concentrations. When the concentration of surfactant below their critical micelle concentration (cmc), force profiles between two emulsion droplets were purely repulsive. As the concentration of SDBS or CTAB above its cmc, the attraction between like-charged O/W emulsion droplets was dominant. The coalescence of the like-charged O/W emulsion droplets is observed. For nonionic surfactants OP-10, even if the cmc had been reached, the attractive force between O/W emulsion droplets couldn’t be measured. Results shows that attractive forces between two like-charged emulsion droplets of several microns in solution can also be induced by ionic micelles and the depletion was enhanced by counterion osmotic pressure. Our work suggests that the effect of micelle-induced depletion on the force between two solid surfaces can be used to predict forces between several micrometers of emulsion droplets.

Influence of tetraalkylammonium salts on the adsorption kinetics of bovine serum albumin in aqueous solutions at the air-liquid interface

Bovine serum albumin adsorption dynamics in water and in aqueous solutions of tetramethylammonium bromide, hexyltrimethylammonium bromide octyltrimethylammonium bromide, decyltrimethylammonium bromide, and dodecyltrimethylammonium bromide at the air-liquid interface was studied at a temperature of 298.15 K.The kinetics of the adsorption process of the biomolecule in water and in the aqueous alkylammonium solutions was investigated following the changes in surface tension with time. The measurements were performed on a high-precision drop volume tensiometer.The surface pressure data were adjusted with two of the most used semi-empirical kinetic models that describe the process of adsorption and allow the determination of the equilibrium adsorption parameters.The results in water and in the aqueous solutions containing tetraalkylammonium salts show that the adsorption kinetics is well described by a model consisting of three steps in which the transport of the protein in the initial stage is diffusion controlled. After some time, the rate is determined by the adsorption and the penetration of the protein at the air-liquid interface and the rearrangement of the protein at the interface; the evolution of both processes is described by steps that follow first-order rate equations.The results indicate that the overall adsorption process of bovine serum albumin BSA in water and the aqueous alkylammonium salts solutions is controlled by the second step which is the slowest of the three steps; it corresponds to the adsorption and penetration of the biomolecule at the air-liquid interface.

Experimental study on heat and mass transfer characteristics between a novel ionic liquid and air under low-humidity conditions

Functional ionic liquids (ILs) are a promising alternative to traditional liquid desiccants. This work is mainly concerned with an experimental investigation on the dehumidification and regeneration performance of an adiabatic falling-film device working with a novel ionic liquid (IL). A specialty of this report is the operation under rather low air temperature as well as low absolute humidity. The effect of air and solution volume flow on the coupled heat and mass transfer coefficient was evaluated based on the state parameters of air and solution by means of the NTU-Lef model. Additionally, aqueous lithium bromide solution (LiBr-H2O) was used for comparison. The results indicated that both IL and LiBr-H2O can dehumidify moist air to nearly 2.2 g/kgda, and the regeneration rate of IL is significantly larger than that of LiBr-H2O. The heat and mass transfer coefficient of IL in dehumidification process is less than that of LiBr-H2O, while the regeneration process is the opposite. It is found that the low wettability of IL on the surface of falling-film plate limits its excellent dehumidification potential, whereas its high mass transfer coefficient in the regeneration process makes up for the disadvantage of poor regeneration potential. Besides, a new correlation for the coupled heat and mass transfer coefficient of IL is proposed. From the perspective of operation optimization, increasing the wettability of IL on falling-film plate will significantly improve the dehumidification rate, and the optimal flow range of IL needs to be considered in the regeneration process. This study establishes a basis for the optimization of heat and mass transfer process between ILs and moist air, and provides guidance for the application of liquid desiccant dehumidification under low-humidity conditions.

Plasmonic structure of zinc (Zn) and zinc oxide (ZnO) on a tapered optical fiber

The authors developed plasmonic structures of zinc (Zn) and zinc oxide (ZnO) on the surface of a tapered optical fiber using optical tweezing. The powdered Zn or ZnO was added to gold nanorods (GNRs) solution and sonicated before tweezing. The concentration of the mixture was 0.5 µg/µl. The GNRs were present in the cetyltrimethylammonium bromide (CTAB) solution. The authors investigated the plasmonic structures and explored the effect of the tweezing conditions on the distribution of the Zn or ZnO on the tapered fiber surface.

Analysis and Experimental Study on Water Vapor Partial Pressure in the Membrane Distillation Process.

In membrane distillation, the vapor pressure difference is the driving force of mass transfer. The vapor pressure is generally assumed by the saturation pressure and calculated by the Antoine equation. However, in the actual operation process, the feed solutions usually flow in a non-equilibrium state, which does not meet the theoretical and measurement conditions of the vapor-liquid equilibrium (VLE) state. This study tested the actual water vapor pressure of the pure water, lithium bromide (LiBr) solution, lithium chloride (LiCl) solution, and calcium chloride (CaCl2) solution under different flow conditions. The results showed that the actual water vapor pressure was lower than the saturation pressure overall, and the difference increased with temperature but decreased with the mass concentration. Therefore, in vacuum membrane distillation (VMD), air gap membrane distillation (AGMD), and sweeping gas membrane distillation (SGMD), the membrane flux calculated by water vapor saturation pressure was higher than the actual membrane flux, and the relative difference decreased and was less than 10% after 60 °C. In direct contact membrane distillation (DCMD), the water vapor pressure difference on both membrane sides was almost the same by using the saturation vapor pressure or the tested data since the pressure errors were partially offset in parallel flow or counter-flow modes.