SH Form Research Articles

Gravity Drainage of Bitumen Induced by Solvent Leaching.

Steam-based thermal recovery processes are energy-intensive and pose environmental concerns due to their high greenhouse gas emissions. The application of solvents has shown promise in reducing the environmental impact of these processes. In this work, the solvent chamber theory is used to study the gravity drainage of bitumen. The results reveal that the drainage rate can be scaled using the thermophysical properties of solvents. The drainage rate is shown to be directly related to the density difference between bitumen and solvent and inversely proportional to the mixture viscosity. A universal scaling relation between the Sherwood number, as a measure of the mass transfer, and Rayleigh number, as a measure of the natural convection, in the form of Sh = βRa is presented using the experimental data of various solvents. This linear relationship is consistent with the theoretical studies of buoyancy-driven convection. Moreover, the scaling prefactor β is found to decrease with increasing natural log of the mobility ratio (α), which results in a lower rate of convective mass transfer. Furthermore, a new critical Rayleigh number equation based on the power-law mixing rule (PLMR) is derived, and the results are compared with the available theories in the literature based on the exponential mixing rule (EMR). The findings provide insights into understanding the convective dissolution with large viscosity contrast. Furthermore, the developed scaling relation provides a useful tool to predict the convective mixing of different bitumen/solvent systems. The results find application in the design of the solvent-based bitumen recovery processes.

Eosinophiluria: accreditation with establishment of an inter-laboratories exchange

Eosinophiluria corresponds to search eosinophils in urine. These are normally absent in urine, their presence could be associated with different clinical conditions affecting kidney or urinary tract. This analysis of medical biology laboratory listed in the French Nomenclature of acts of medical biology has to be validated according to norm NF EN ISO 15189. The principle of eosinophiluria method is based on eosinophils quantification by optical microscopy in a urine sample (urination) after staining. The aim of this article is to provide to biologists the eosinophiluria's clinical interest, but also bibliographic, technical and practical elements that can help them to establish eosinophiluria in their laboratories. The method validation elements were described for each item of SH Form 43. They include the analysis risks study, inter-operator variability, uncertainties, measurement range, comparison of methods based on the comparison of two staining, interferences, robustness, reliability of reagents, reference interval. Regarding accuracy, in absence of external quality assessment for this analysis, an inter-laboratory exchange has been set up in accordance with the requirements of the norm. Its organization is described. The performance of eosinophiluria was verified, recalling the importance of the pre-analytical conditions and the quality of staining. All of these data are presented and led the accreditation of eosinophiluria in our laboratory.

Influence of humic acid structure on the accumulation of oxyfluorfen in tropical soils of mountain agroecosystems

Herbicide application is a practice commonly used in agricultural systems because it is an efficient method of weed control. An inherent characteristic of some herbicides used in mountain agriculture, such as oxyfluorfen, is high adsorption to soil organic matter (SOM). Thus, intensive management that changes the quantity and quality of SOM, such as soil tillage and the massive application of organic fertilizers such as poultry litter, may favor soil contamination by this herbicide and alter its dynamics in the environment. Therefore, this study aimed to characterize the structures of humic substances (HSs) in the soil of forest areas and areas with intensive production of vegetables, relating them to the accumulation of the herbicide oxyfluorfen in tropical mountain agroecosystems. Organic carbon content was quantified in HSs, humic acid (HAs) were structurally characterized by CP/MAS 13C-NMR spectroscopy, and the oxyfluorfen molecule was detected and quantified using the QuEChERS residue detection method with subsequent analysis by LC-MS/MS. Oxyfluorfen was not detected in the forest areas, but it was detected in the vegetable growing areas at points with the lowest slope and high contents of organic matter and clay, with values of up to 0.13 mg kg−1. The intensification in the SOM mineralization process, promoted by the intensive management adopted in the vegetable growing areas, resulted in a 16.46% reduction in COT, a 58.84% reduction in the carbon content in the form of SH and a reduction in the structures that give recalcitrance to the HA molecule (CAlkyl-H,R, CCOO–H,R, CAromatic-H,R, and CAromatic-O) when compared to those values in the forest area, presenting HAs with more aliphatic and labile properties. Thus, due to the structural characteristics of the HAs in the vegetable production areas, the herbicide oxyfluorfen showed a close relationship with the more aliphatic oxygenated structures, namely, CAlkyl-O,N, CAlkyl-O and CAlkyl-di-O.

A comparative study on non‐Newtonian fractional‐order Brinkman type fluid with two different kernels

AbstractThis study carried out the free convective non‐Newtonian fluid of Brinkman type flow near an upright plate moving with velocity f(t). A fractional order model for non‐Newtonian fluid of Brinkman type flow is proposed. The time derivative in the proposed fractional flow model is considered by using the two types of fractional derivatives namely Caputo fractional derivative and Atangana–Baleanu fractional derivative. The system of conjugated fractional partial differential equations for the temperature θ, velocity u and concentration C are worked out by applying optimal homotopy asymptotic technique. The effectuate of tangible and fractional variables on the domains of velocity u, temperature θ and concentration C are envisioned graphically. The rate of heat and mass transfer in the form of Nu and Sh is also calculated for both fractional derivatives. The numerical results reveal the efficiency, reliability, significant features, and simple in computation with high accuracy of consider method for non‐Newtonian fractional order fluid of Brinkman type flow. We ascertained that our results are in excellent agreement with the exact results.

Preparation of REE-doped Ge-based chalcogenide glasses with low hydrogen impurity content

The Ga5Ge36S59 and Ga5Ge36Se59 glass samples doped with 760–3800 ppm(at) ions of thulium, praseodymium and terbium are prepared. The addition of the rare-earth element (REE) in the conventional glass manufacturing process is shown to lead to a significant increase in the content of hydrogen impurity in chalcogenide glasses. A new technique for producing REE-doped glasses, including the preliminary melting of gallium with rare earth element in an evacuated silica-glass reactor at a temperature of 700 °C, is proposed. The advantage of the proposed technique is the effective removal of hydrogen impurity from REE due to the thermal decomposition of their hydrides and hydroxides. The total hydrogen content in the form of SH-, SeH-groups and GeH in the best glass samples was 0.2–0.4 ppm(at).

Numerical study on the response of the largest lake in China to climate change

Abstract. Lakes are sensitive indicators of climate change. There are thousands of lakes on the Tibetan Plateau (TP), and more than 1200 of them have an area larger than 1 km2; they respond quickly to climate change, but few observation data of lakes are available. Therefore, the thermal condition of the plateau lakes under the background of climate warming remains poorly understood. In this study, the China regional surface meteorological feature dataset developed by the Institute of Tibetan Plateau Research, Chinese Academy of Sciences (ITPCAS), MODIS lake surface temperature (LST) data and buoy observation data were used to evaluate the performance of lake model FLake, extended by simple parameterizations of the salinity effect, for brackish lake and to reveal the response of thermal conditions, radiation and heat balance of Qinghai Lake to the recent climate change. The results demonstrated that the FLake has good ability in capturing the seasonal variations in the lake surface temperature and the internal thermal structure of Qinghai Lake. The simulated lake surface temperature showed an increasing trend from 1979 to 2012, positively correlated with the air temperature and the downward longwave radiation while negatively correlated with the wind speed and downward shortwave radiation. The simulated internal thermodynamic structure revealed that Qinghai Lake is a dimictic lake with two overturn periods occurring in late spring and late autumn. The surface and mean water temperatures of the lake significantly increased from 1979 to 2012, while the bottom temperatures showed no significant trend, even decreasing slightly from 1989 to 2012. The warming was the strongest in winter for both the lake surface and air temperature. With the warming of the climate, the later ice-on and earlier ice-off trend was simulated in the lake, significantly influencing the interannual and seasonal variability in radiation and heat flux. The annual average net shortwave radiation and latent heat flux (LH) both increase obviously while the net longwave radiation and sensible heat flux (SH) decrease slightly. Earlier ice-off leads to more energy absorption mainly in the form of shortwave radiation during the thawing period, and later ice-on leads to more energy release in the form of longwave radiation, SH and LH during the ice formation period. Meanwhile, the lake–air temperature difference increased in both periods due to shortening ice duration.

Experimental Assignment of Disulfide‐Bonds in Purified Proteins

The formation of disulfide bonds in proteins is an important post-translational modification that is critical for stabilizing the native structures of proteins, particularly proteins exposed to oxidizing environments. For this reason, most cysteines in secreted proteins or protein domains on the surface of the cell are in disulfides, whereas most cysteines in the cytoplasm are in the unmodified -SH form. Disulfide linkages must be experimentally determined, as they cannot be predicted from amino acid sequence. These assignments provide insights into three-dimensional structure and contribute to the understanding of structural-functional relationships. This unit details a series of protocols that have been applied successfully to map disulfide bonds in proteins. The general strategy involves chemical or proteolytic cleavage of the protein followed by chromatographic separation of the resultant peptides. Mass spectrometry is used to identify disulfide-containing peptides and determine sites of disulfide linkage. A partial reduction and alkylation strategy for mapping disulfide linkages in peptides with multiple disulfide bonds is also presented. © 2019 by John Wiley & Sons, Inc.

Legionella pneumophila utilizes a single-player disulfide-bond oxidoreductase system to manage disulfide bond formation and isomerization.

Legionella pneumophila uses a single homodimeric disulfide bond (DSB) oxidoreductase DsbA2 to catalyze extracytoplasmic protein folding and to correct DSB errors through protein-disulfide isomerase (PDI) activity. In Escherichia coli, these functions are separated to avoid futile cycling. In L. pneumophila, DsbA2 is maintained as a mixture of disulfides (S-S) and free thiols (SH), but when expressed in E. coli, only the SH form is observed. We provide evidence to suggest that structural differences in DsbB oxidases (LpDsbB1 and LpDsbB2) and DsbD reductases (LpDsbD1 and LpDsbD2) (compared with E. coli) permit bifunctional activities without creating a futile cycle. LpdsbB1 and LpdsbB2 partially complemented an EcdsbB mutant while neither LpdsbD1 nor LpdsbD2 complemented an EcdsbD mutant unless DsbA2 was also expressed. When the dsb genes of E. coli were replaced with those of L. pneumophila, motility was restored and DsbA2 was present as a mixture of redox forms. A dominant-negative approach to interfere with DsbA2 function in L. pneumophila determined that DSB oxidase activity was necessary for intracellular multiplication and assembly/function of the Dot/Icm Type IVb secretion system. Our studies show that a single-player system may escape the futile cycle trap by limiting transfer of reducing equivalents from LpDsbDs to DsbA2.

Disulfide bonds regulate binding of exogenous ligand to human cytoglobin

Cytoglobin (Cgb) was discovered a decade ago and is a fourth member of the group of hexacoordinated globin-folded proteins. Although some crystal structures have been reported and several functions have been proposed for Cgb, its physiological role remains uncertain. In this study, we measured cyanide binding to the ferric state of the wild-type (WT) Cgb, and found that the binding consisted of multiple steps. These results indicated that Cgb may be comprised of several forms, and the presence of monomers, dimers, and tetramers was subsequently confirmed by SDS-PAGE. Remarkably, each species contained two distinguishable forms, and, in the monomer, analyses of alternative cysteine states suggested the presence of an intramolecular disulfide bond (monomer SS form) and a structure with unpaired thiol groups (monomer SH form). These confirmed that forms were separated by gel-exclusion chromatography, and that the cyanide binding of the separated fractions was again measured; they showed different affinities for cyanide, with the monomer fraction showing the highest affinity. In addition, the ferrous state in each fraction showed distinct carbon monoxide (CO)-binding properties, and the affinities for cyanide and CO suggested a linear correlation. Furthermore, we also prepared several variants involving the two cysteine residues. The C38S and C83S variants showed a binding affinity for cyanide similar to the value for the monomer SH form, and hence the fraction with the highest affinity for exogenous ligands was designated as a monomer SS form. We concluded that polymerization could be a mechanism that triggers the exertion of various physiological functions of this protein and that an appropriate disulfide bond between the two cysteine residues was critical for regulating the binding affinity of Cgb, which can act as a ROS scavenger, for exogenous ligands.

Morphological, ecological and mtDNA sequence variation in coregonid fish from the Baunt Lake system (the Vitim River basin)

We performed morphological, ecological and genetic analyses of taxonomically complex sympatric whitefi sh forms inhabiting the Baunt Lake system in the Vitim River basin, Transbaikalia. It was shown that the whitefi sh forms in this system clearly differed based on morphological traits, growth rate and diet. The most signifi cant differences were based on the number of gill rakers, while the number of lateral line scales was similar. These whitefi sh had distinct diets, namely euryphagous and planktivorous diets. We developed a phylogeny of mtDNA haplotypes among the whitefi sh species and populations from the Baunt Lake system and the headwater regions of the Ob and Yenisei River basins. A morphologically homogeneous cisco-like whitefi sh sample revealed two distinct mitochondrial lineages. A strong genetic divergence between the fi rst mitochondrial lineage of cisco-like whitefi sh and all of the studied whitefi sh forms was revealed. We analyzed alternative hypotheses regarding the ori gin of cisco-like whitefi sh and the densely rakered whitefi sh form from the Baunt Lake system.

Process intensification of catalytic hydrogenation of ethylanthraquinone with gas‐liquid microdispersion

AbstractIn this article, to miniaturize the hydrogenation reactor and make the H2O2 production with more safety a gas‐liquid microdispersion system was generated to intensify the process of catalytic hydrogenation of ethylanthraquinone by passing the gas‐liquid microdispersion system through a generally packed bed reactor. A microdispersion device with a 5 μm pore size microfiltration membrane as the dispersion medium has been developed and microbubbles in the size of 10–100 μm were successfully generated. The reaction and mass transfer performance was evaluated. The conversion of ethylanthraquinone as much as 35% was realized in less than 3.5 s. The overall volume mass transfer coefficient in the microdispersion reaction system reached in the range of 1–21 s−1, more than two orders of magnitude larger than the values in normal gas‐liquid trickle‐bed reactors. A mathematical model in the form of Sh = 2.0 + 54.7Sc1/3We1/2ϕ1/10 has been firstly suggested, which can well predict the overall mass transfer coefficient. © 2011 American Institute of Chemical Engineers AIChE J, 2012

Improving the Diffusion Controlled Cementation of Cadmium Ions Using Reciprocating Fixed Bed of Zinc Rings

The aim of the present work is to investigate the effect of pulsation on improving the rate of the diffusion controlled cementation of cadmium ions using reciprocating fixed bed of zinc rings. The kinetics of the cementation reaction was investigated under different conditions of initial concentration of cadmium ions, frequency and amplitude of oscillation (vibration velocity), zinc ring diameter, bed diameter, bed height and temperature. The effect of temperature was found to fit the Arrhenius equation with an activation energy of 7.58 kcal/mole which confirms the diffusion controlled nature of the reaction. A dimensionless correlation in the form of Sh = 6.9 Re0.45 Sc0.33 (Bd/Bh)0.89 was deduced. The industrial application of the obtained results was discussed.

Decrease in Size of Hen Egg white Lysozyme Aggregates with Decrease in Monomer Concentration from Micro to Nanomolar in Alkaline pH

Earlier work from our laboratory has demonstrated that hen egg white lysozyme (HEWL) is an excellent model protein for investigating protein aggregation at an alkaline pH of 12.2. Exposure of HEWL to this pH at monomer concentrations from 0.3 to 120 uM, yielded amyloid fibrils as shown previously. Here we present the following concentration dependent changes observed with HEWL aggregates subsequent to incubation at pH 12.2 at room temperature from 0 to 24 hours. A) a two-fold increase in exposure of trp residues in HEWL to water at 0.3 uM compared to 120 uM as revealed by fluorescence quenching experiments with iodide B) a several fold increase in ANS fluorescence intensity accompanied by significantly blue-shifted emission on binding to HEWL moving from 0.3 to 120 uM. C) a marginal increase in dansyl probe fluorescence intensity accompanied by significant blue-shifted dansyl emission in dansyl conjugated HEWL moving from 0.3 to 120 uM. D) a gradual increase in steady state fluorescence anisotropy of dansyl probe in dansyl conjugated HEWL moving from 3 to 120 uM, although the dansyl mean fluorescence lifetime remained concentration independent between 3 and 120 uM. E) presence of all cys in -SH form with absence of any change in free [-SH] between 20 & 120 uM, as revealed by DTNP assays. In addition, FCS measurements with rhodamine conjugated HEWL demonstrated facile aggregation of HEWL in the concentration range 25 nM to 120 uM. The above results imply that, the size of HEWL aggregates, are clearly dependent on the initial monomer concentration, with lower concentrations like 300 nM favoring small aggregates that possess solvent exposed trp, diminished binding towards ANS and shorter mean fluorescence lifetime for dansyl probe.

Oxidative Status of DJ-1-dependent Activation of Dopamine Synthesis through Interaction of Tyrosine Hydroxylase and 4-Dihydroxy-l-phenylalanine (l-DOPA) Decarboxylase with DJ-1

Parkinson disease (PD) is caused by loss of dopamine, which is synthesized from tyrosine by two enzymes, tyrosine hydroxylase (TH) and 4-dihydroxy-L-phenylalanine decarboxylase (DDC). DJ-1 is a causative gene for the familial form of PD, but little is known about the roles of DJ-1 in dopamine synthesis. In this study, we found that DJ-1 directly bound to TH and DDC and positively regulated their activities in human dopaminergic cells. Mutants of DJ-1 found in PD patients, including heterozygous mutants, lost their activity and worked as dominant-negative forms toward wild-type DJ-1. When cells were treated with H(2)O(2), 6-hydroxydopamine, or 1-methyl-4-phenylpyridinium, changes in activities of TH and DDC accompanied by oxidation of cysteine 106 of DJ-1 occurred. It was found that DJ-1 possessing Cys-106 with SH and SOH forms was active and that DJ-1 possessing Cys-106 with SO(2)H and SO(3)H forms was inactive in terms of stimulation of TH and DDC activities. These findings indicate an essential role of DJ-1 in dopamine synthesis and contribution of DJ-1 to the sporadic form of PD.

Cysteine S-Nitrosylation Protects Protein-tyrosine Phosphatase 1B against Oxidation-induced Permanent Inactivation

Protein S-nitrosylation mediated by cellular nitric oxide (NO) plays a primary role in executing biological functions in cGMP-independent NO signaling. Although S-nitrosylation appears similar to Cys oxidation induced by reactive oxygen species, the molecular mechanism and biological consequence remain unclear. We investigated the structural process of S-nitrosylation of protein-tyrosine phosphatase 1B (PTP1B). We treated PTP1B with various NO donors, including S-nitrosothiol reagents and compound-releasing NO radicals, to produce site-specific Cys S-nitrosylation identified using advanced mass spectrometry (MS) techniques. Quantitative MS showed that the active site Cys-215 was the primary residue susceptible to S-nitrosylation. The crystal structure of NO donor-reacted PTP1B at 2.6 A resolution revealed that the S-NO state at Cys-215 had no discernible irreversibly oxidized forms, whereas other Cys residues remained in their free thiol states. We further demonstrated that S-nitrosylation of the Cys-215 residue protected PTP1B from subsequent H(2)O(2)-induced irreversible oxidation. Increasing the level of cellular NO by pretreating cells with an NO donor or by activating ectopically expressed NO synthase inhibited reactive oxygen species-induced irreversible oxidation of endogenous PTP1B. These findings suggest that S-nitrosylation might prevent PTPs from permanent inactivation caused by oxidative stress.

설프히드릴 변형 화합물질들에 의한 양배추 포스포리파제 D의 시스테인 잔기의 특성

SH group modifying chemicals were used to characterize the eight cysteine residues of cabbage PLD. 5,5-dithiobis(2-nitrobenzoate)(DTNB) was used to titrate the SH group of cysteine residues . Based on the optical density at 412nm due to the reduced DTNB, 4 SH groups are found to be present in a native PLD while 8 SH groups in the denatured PLD whose tertiary structure was perturbed by 8M urea. The results imply that among the 8 cysteine residues of PLD, the half(4) are exposed on the surface whereas the other half are present at the interior of the enzyme tertiary structure. The PLD was inactivated by SH modifying reagents such as p-chloromercuribenzoate(PCMB), iodoacetate, iodoacetamide, and N-ethylmaleimide. At the addition of dithiothreitol(DTT) only the PCMB inhibited PLD activity was recovered reversibly. The micro-environment of the exposed SH group of cysteine residues was examined with various disulfide compounds with different functional groups and we found that anionic or neutral disulfides appear to be more effective than the positively charged cystamine for inactivating the PLD activity. The effect of redox state of cysteine residues on the PLD activity was further explored with H2O2. The oxidation of SH groups by H2O2 inhibited the PLD activity more than 70%, which was mostly recovered by DTT. From these results, we could confirm chemically that all the cysteine residues of PLD are present as in their reduced SH forms and the 4 SH groups exposed on the surface of the enzyme may play important roles in the regulation of PLD activity.

Analysis of the Ortho Effect: Basicity of 2-Substituted Benzonitriles

Energies of 18 ortho-substituted benzonitriles and their protonated forms were calculated within the framework of the density functional theory at the level B3LYP/6-311+G(d,p). The substituent effects were evaluated in terms of isodesmic reactions as the effects on the basicity on the one hand and separately in the nitrile molecules and in the cations on the other. The ortho effect was defined as the difference when compared to the 4-substituted isomers. It is smaller than in the case of ortho-substituted benzoic acids but not negligible (up to 25 kJ mol-1). In unprotonated molecules it may be classified as purely steric effect, in spite of the small dimension of the CN group and estimates made with the calotte models. In the protonated forms, polar properties of the substituent are decisive. In addition, a new, quite important substituent effect was discovered with the substituents OH, SH, CHO and COOCH3, which is controlled by different conformation of protonated and unprotonated molecules. Substituents OH, SH and NH2 form also weak hydrogen bonds in unprotonated nitriles. In summary, 2-substituted benzonitriles allowed evaluating of several, partly new substituent effects but cannot serve as model molecules without an ortho effect, although the constant functional group CN is sterically little pretentious.

Characterization of cysteinylation of pharmaceutical‐grade human serum albumin by electrospray ionization mass spectrometry and low‐energy collision‐induced dissociation tandem mass spectrometry

Three samples of albumin derived from human plasma (pharmaceutical grade, HSA) obtained from different commercial sources were investigated for their micro-heterogeneities by means of electrospray ionization (ESI) ion trap mass spectrometry (ITMS). The study covered MS analyses of the intact proteins as well as on the tryptic peptide level. The intact protein samples were analyzed without any separation step except for simple desalting. With these samples we observed in the positive ion ESI mass spectra that the multiply charged ion signals of HSA consisted of a number of fully or partly resolved peaks with relative intensities depending on the analyzed sample. The non-modified form of HSA was detected in the three HSA preparations at m/z values of 66448 +/- 3.6, 66450 +/- 0.6 and 66451 +/- 3.2 ([MH]+), respectively. The value calculated from the amino acid sequence was 66439. The second compound present with high intensity (in two cases the base peak in the deconvoluted mass spectrum) is interpreted as a modified HSA, and the molecular mass increase in relation to the unmodified HAS was between 116 and 118 Da (m/z of 66 564, 66 567 and 66 569), suggesting the presence of a covalently bound cysteine residue. A further peak in the deconvoluted ESI spectra was found in all three samples with rather low signal/noise ratio at m/z 66 619, 66 621 and 66 613, respectively, which may correspond to a non-enzymatic glycation described in the literature. The verification of the proposed covalent HSA modifications was subsequently done on the peptide level using high-performance liquid chromatography (HPLC)/ESI-MS and HPLC/ESI-MS/MS including low-energy collision-induced dissociation (CID). Prior to the tryptic digestion, the HSA samples were alkylated without a prior reduction step. Following this procedure we detected peptides of the sequence T21-41 that included the Cys-34 residue in both forms: cysteinylated (m/z 639.15 [M+4H]4+) as well as vinylpyridine-alkylated (m/z 635.69 [M+4H]4+, which means in its previously native free SH form). In the next step on-line LC/ESI low-energy CID MS/MS experiments were performed to verify these two proposed structures. By means of MS/MS analysis of the mentioned ions the described modification (cysteinylation) at the Cys-34 residue could be proven. This abundant modification of HSA in pharmaceutical-grade preparations could be unambiguously identified as cysteinylation at the Cys-34 residue. On the other hand, the proposed non-enzymatic glycation was not detectable on the peptide level in the on-line HPLC/ESI-MS mode, maybe due to the low concentration in the three samples under investigation.

Modelling of zinc transport through a supported liquid membrane

The transport of zinc (II) from an aqueous solution containing zinc (II), iron (II), calcium (II) and magnesium (II) through supported liquid membrane using di-2-ethylhexyl phosphoric acid dissolved in kerosene as a mobile carrier was studied. The effects of temperature, rate of feed and stripping phase and concentration of stripping phase on the mass transfer coefficients of aqueous boundary layers and membrane were studied. A transport rate model has been derived taking into account diffusion through the feed side aqueous boundary layer, diffusion of carrier–zinc complex through the supported liquid membrane and diffusion through the stripping side aqueous boundary layer as simultaneous controlling factors. The mass transfer coefficient data of the side of the feed phase were correlated in the form of Sh = 0.0047 Re 1.349 Sc 0.3333. This correlation was used to calculate the mass transfer coefficient of the aqueous film at the side of the stripping phase. For some parameters and their levels, the mass transfer coefficients, k f, k m and k s (m s − 1 ), were calculated.

Kinetics of adsorption of hydrocarbon chloro-derivatives from seven-component aqueous solution onto a thin layer of DTO-activated carbon

The mass transfer and effective intraparticle diffusion coefficients were determined in the adsorption process of 1,2-dichloroethane, 1,1,2,2-tetrachloroethane, chloroform, carbon tetrachloride, 1,1-dichloroethene, perchloroethene, and 1,1,2-trichloroethene from seven-component aqueous solution onto a thin layer of activated carbon. A modified constant-volume method was used in the studies. A correlation between similarity numbers in the form of Sh = 2 + 1.54 Re 0.66 Sc 0.33 was derived for a range of the Reynolds numbers ∈ ( 1 – 15 ) . Based on the Biot number, it was found that within the range of Reynolds numbers <14 the mass transport through a film decides the adsorption rate.