Initial Rate Constants Research Articles

Ester catalytic hydrolysis by a tridentate N,N′,N″-copper bridged cyclodextrin dimer

Abstract A new pyridine bridged cyclodextrin dimer mono-copper complex (CuL) was synthesized and characterized. The hydrolysis of carboxylic acid esters, bis(4-nitrophenyl)carbonate (BNPC) and 4-nitrophenyl acetate (NA), and phosphate ester, a DNA model bis(4-nitrophenyl)phosphate (BNPP), promoted by CuL has been investigated. The resulting hydrolysis rate constants showed that CuL had a very high rate of catalysis for BNPC hydrolysis, yielding a 2.73 × 103-fold rate enhancement over uncatalyzed hydrolysis at pH 7.00, compared to only a 78.2-fold rate enhancement for NA hydrolysis. The initial first-order rate constant of catalytic hydrolysis for BNPP was 1.01 × 10−7 s−1 at pH 8.5, 35 °C and 0.1 mM catalyst concentration, about 1260-fold acceleration over uncatalyzed hydrolysis. The second rate constant kBNPP of BNPP hydrolysis promoted by CuL was found to be 5.94 × 10−4 M−1 s−1.

Sorption of SO 2 and NO from simulated flue gas over rice husk ash (RHA)/CaO/CeO 2 sorbent: Evaluation of deactivation kinetic parameters

In this study, the kinetic parameters of rice husk ash (RHA)/CaO/CeO 2 sorbent for SO 2 and NO sorptions were investigated in a laboratory-scale stainless steel fixed-bed reactor. Data experiments were obtained from our previous results and additional independent experiments were carried out at different conditions. The initial sorption rate constant ( k 0) and deactivation rate constant ( k d) for SO 2/NO sorptions were obtained from the nonlinear regression analysis of the experimental breakthrough data using deactivation kinetic model. Both the initial sorption rate constants and deactivation rate constants increased with increasing temperature, except at operating temperature of 170 °C. The activation energy and frequency factor for the SO 2 sorption were found to be 18.0 kJ/mol and 7.37 × 10 5 cm 3/(g min), respectively. Whereas the activation energy and frequency factor for the NO sorption, were estimated to be 5.64 kJ/mol and 2.19 × 10 4 cm 3/(g min), respectively. The deactivation kinetic model was found to give a very good agreement with the experimental data of the SO 2/NO sorptions.

Stopped-Flow NMR: Determining the Kinetics of [rac-(C2H4(1-indenyl)2)ZrMe][MeB(C6F5)3]-Catalyzed Polymerization of 1-Hexene by Direct Observation

Stopped-flow NMR measurements suitable for determination of reaction kinetics on time scales of 100 ms or longer have been achieved by adaptation of a commercial NMR flow probe with a high-efficiency mixer and drive system. Studies of metallocene-catalyzed alkene polymerization at room temperature have been complicated by high rates, imprecise knowledge of the distribution of different catalyst species with time, and the high sensitivity of the catalysts to low concentrations of impurities. Application of the stopped-flow NMR method to the study of the kinetics of 1-hexene polymerization in the presence of (EBI)ZrMe[MeB(C(6)F(5))(3)] demonstrates that NMR spectroscopy provides an efficient method for direct and simultaneous measurement of substrate consumption and catalyst speciation as a function of time. Kinetic modeling of the catalyst and substrate concentration time courses reveal efficient determination of initiation, propagation, and termination rate constants. As first suggested by Collins and co-workers (Polyhedron 2005, 24, 1234-1249), a kinetic model in which Zr-HB(C(6)F(5))(3) forms rapidly upon beta-hydride elimination but reacts relatively slowly with alkene to reinitiate chain growth is supported by these data.

Probing Ligand-binding Pockets of the Mevalonate Pathway Enzymes from Streptococcus pneumoniae

Diphosphomevalonate (Mev.pp) is the founding member of a new class of potential antibiotics targeting the Streptococcus pneumoniae mevalonate (Mev) pathway. We have synthesized a series of Mev.pp analogues designed to simultaneously block two steps in this pathway, through allosteric inhibition of mevalonate kinase (MK) and, for five of the analogues, by mechanism-based inactivation of diphosphomevalonate decarboxylase (DPM-DC). The analogue series expands the C(3)-methyl group of Mev.pp with hydrocarbons of varying size, shape, and chemical and physical properties. Previously, we established the feasibility of a prodrug strategy in which unphosphorylated Mev analogues could be enzymatically converted to the active Mev.pp forms by the endogenous MK and phosphomevalonate kinase. We now report the kinetic parameters for the turnover of non-, mono-, and diphosphorylated analogues as substrates and inhibitors of the three mevalonate pathway enzymes. The inhibition of MK by Mev.pp analogues revealed that the allosteric site is selective for compact, electron-rich C(3)-subsitutents. The lack of reactivity of analogues with DPM-DC provided evidence, counter to the existing model, for a decarboxylation transition state that is concerted rather than dissociative. The Mev pathway is composed of three structurally and functionally conserved enzymes that catalyze consecutive steps in a metabolic pathway. The current work reveals that these enzymes exhibit significant differences in specificity toward R-group substitution at C(3) and that these patterns are explained well by changes in the volume of the C(3) R-group-binding pockets of the enzymes.

Oxidation of 2,6-Di-tert-butylphenol by dioxygen catalyzed by tetrasodium phthalocyaninatocobalt(II) tetrasulfonate in aqueous micellar media

The oxidation of 2,6-di-tert-butylphenol by dioxygen has been investigated in aqueous micellar aggregates of cetyltrimethylammonium bromide (CTAB) using tetrasodium phthalocyaninatocobalt(II) tetrasulfonate (CoPcTsNa4) as catalyst. The CTAB/CoPcTsNa4 system showed enhanced catalytic activity in the oxidation of 2,6-di-tert-butylphenol compared to that observed in the oxidation reaction in the absence of CTAB. 2,6-Di-tert-butyl-1,4-benzoquinone and 3,5,3′,5′-tetra-tert-butyl-4,4-diphenoquinone were identified as reaction products. The initial rate constants of auto-oxidation reaction was found to increase with increasing the pH range from 7.0 to 13.0. The rate constants kobs of auto-oxidation reaction showed linear dependence on catalyst concentration. The rate of auto-oxidation reaction was found to fit a Michealis-Menten kinetic model for the saturation of catalyst sites with increasing 2,6-di-tert-butylphenol concentration and dioxygen pressure. Tetrasodium phthalocyaninatocobalt(II) tetrasulfonate in aqueous micellar solution of CTAB was found to be mainly monomeric.

Information content of incubation experiments for inverse estimation of pools in the Rothamsted carbon model: a Bayesian perspective

Abstract. A major drawback of current soil organic carbon (SOC) models is that their conceptually defined pools do not necessarily correspond to measurable SOC fractions in real practice. This not only impairs our ability to rigorously evaluate SOC models but also makes it difficult to derive accurate initial states of the individual carbon pools. In this study, we tested the feasibility of inverse modelling for estimating pools in the Rothamsted carbon model (ROTHC) using mineralization rates observed during incubation experiments. This inverse approach may provide an alternative to existing SOC fractionation methods. To illustrate our approach, we used a time series of synthetically generated mineralization rates using the ROTHC model. We adopted a Bayesian approach using the recently developed DiffeRential Evolution Adaptive Metropolis (DREAM) algorithm to infer probability density functions of the various carbon pools at the start of incubation. The Kullback-Leibler divergence was used to quantify the information content of the mineralization rate data. Our results indicate that measured mineralization rates generally provided sufficient information to reliably estimate all carbon pools in the ROTHC model. The incubation time necessary to appropriately constrain all pools was about 900 days. The use of prior information on microbial biomass carbon significantly reduced the uncertainty of the initial carbon pools, decreasing the required incubation time to about 600 days. Simultaneous estimation of initial carbon pools and decomposition rate constants significantly increased the uncertainty of the carbon pools. This effect was most pronounced for the intermediate and slow pools. Altogether, our results demonstrate that it is particularly difficult to derive reasonable estimates of the humified organic matter pool and the inert organic matter pool from inverse modelling of mineralization rates observed during incubation experiments.

The influence of hydrogen pressure on the heterogeneous hydrogenation of β-myrcene in a CO 2-expanded liquid

This paper presents the second part of work on the effect of hydrogen partial pressure on the hydrogenation of a terpene in a CO 2-expanded liquid. The effect of hydrogen partial pressure on the hydrogenation of β-myrcene possessing three C C bonds catalysed by alumina-supported ruthenium and rhodium was studied. Experiments were performed at various hydrogen pressures in the range from 2.0 up to 4.5 MPa at a fixed total pressure of 12.5 MPa. In all the conditions the reaction proceeded in two phases (liquid + gas), that is, the total pressure was below the critical pressure of the CO 2 + β-myrcene + H 2 system. The liquid phase volume is expanded in relation to the initial volume of β-myrcene in a fashion that is strongly dependent on the hydrogen and carbon dioxide pressures. An increase of H 2 pressure concomitantly diminishes carbon dioxide pressure, which leads to the enhancement of the liquid phase in hydrogen and a terpene. It does not direct to straightforward higher reaction rate, but surprisingly the effect of higher concentrations either hydrogen or β-myrcene is opposite. It is attributed to the fact that the hydrogenation of β-myrcene rate-controlling factor turns out to be the hydrogen to β-myrcene ratio which decreases as the hydrogen pressure increases. These unexpected appealing results present that lower pressures of hydrogen guide to higher hydrogen/β-myrcene ratios in the liquid phase, but on the other hand they also amplify the initial reaction rate constant. The obtained results are opposite to the results achieved for effect of hydrogen pressure on the Pd-catalysed hydrogenation of limonene consisting of two C C double bonds.

Modelling of carrier mediated transport of chromium(III) in the supported liquid membrane system with D2EHPA

The facilitated transport of Cr(III) in the SLM system with D2EHPA, was investigated with respect to the composition of feed phase (type of Cr(III) salt, initial Cr(III) concentration, initial ionic strength) and organic phase (carrier concentration and type of diluent) and also volume phase ratio. The effect of diluents on the initial flux and rate constant was expressed by means of their solvatochromic parameters and Leggett modification of Kamlet and Taft model of solute–solvent interactions.

Lipid Transfer Mediated by a Recombinant Pro-Sterol Carrier Protein 2 for the Accurate Preparation of Asymmetrical Membrane Vesicles Requires a Narrow Vesicle Size Distribution: A Free-Flow Electrophoresis Study

We applied protein-mediated lipid transfer using recombinant His-tagged pro-sterol carrier protein 2 (pro-SCP2) to prepare asymmetrical membrane vesicles (AMV) featuring an unequal transmembrane distribution of the negative phospholipid egg-phosphatidylglycerol (EPG). Pure egg-phosphatidylcholine (EPC) vesicles were used as the acceptor and EPC:EPG 90:10 mol % vesicles as the donor populations. The changes in surface charge during EPG transfer were used to quantify the degree of asymmetry by free-flow electrophoresis (FFE). The relative deflection in FFE correlated with EPG content in the outer monolayer (x(EPG)). The initial transfer rates and first order rate constants for the transfer process were determined. The addition of pro-SCP2 at a molar protein-to-lipid ratio R(P/L) of (15-20) x 10(-5) accelerated the EPG transfer to half-times of between 2 and 3 h. Thus, the transmembrane redistribution of EPG by flip-flop, which reduces the degree of asymmetry and occurs at half-times of tens of hours, was minimized during the transfer process. We investigated the influence of membrane curvature on the transfer rate using 50 and 100 nm vesicles with very low size distribution widths (RSD of 13-17%). Transfer occurred with a 55.7% higher initial rate between the smaller vesicles. The use of equally sized acceptor and donor populations of such narrow size distributions was shown to be important for the preparation of AMV with a uniform degree of asymmetry. Under these conditions, AMV were obtained after less than 3 h by preparative FFE separation. In the case of the acceptor vesicles, EPG transfer increased x(EPG) to 3 mol %, whereas it was reduced to 6 mol % in the donor vesicles.

Silica Nanoparticles To Control the Lipase-Mediated Digestion of Lipid-Based Oral Delivery Systems

We investigate the role of hydrophilic fumed silica in controlling the digestion kinetics of lipid emulsions, hence further exploring the mechanisms behind the improved oral absorption of poorly soluble drugs promoted by silica-lipid hybrid (SLH) microcapsules. An in vitro lipolysis model was used to quantify the lipase-mediated digestion kinetics of a series of lipid vehicles formulated with caprylic/capric triglycerides: lipid solution, submicrometer lipid emulsions (in the presence and absence of silica), and SLH microcapsules. The importance of emulsification on lipid digestibility is evidenced by the significantly higher initial digestion rate constants for SLH microcapsules and lipid emulsions (>15-fold) in comparison with that of the lipid solution. Silica particles exerted an inhibitory effect on the digestion of submicrometer lipid emulsions regardless of their initial location, i.e., aqueous or lipid phases. This inhibitory effect, however, was not observed for SLH microcapsules. This highlights the importance of the matrix structure and porosity of the hybrid microcapsule system in enhancing lipid digestibility as compared to submicrometer lipid emulsions stabilized by silica. For each studied formulation, the digestion kinetics is well correlated to the corresponding in vivo plasma concentrations of a model drug, celecoxib, via multiple-point correlations (R(2) > 0.97). This supports the use of the lipid digestion model for predicting the in vivo outcome of an orally dosed lipid formulation. SLH microcapsules offer the potential to enhance the oral absorption of poorly soluble drugs via increased lipid digestibility in conjunction with improved drug dissolution/dispersion.

Degradação fotoeletrocatalítica do corante azul básico 41 usando semicondutor nanoporoso de Ti/TiO2

O presente trabalho investiga a degradação fotoeletrocatalítica do corante Azul Básico 41 (AB 41) amplamente utilizado na tintura de fibras sintéticas, utilizando um semicondutor Ti/TiO2 como fotoanodo. 100% de degradação foi obtida após 60 min de tratamento de 8,33x10-5 mol L-1 do corante em 0,1 mol L−1 Na2SO4, pH 2 sob densidade de corrente de 0,40 mA cm−2 e irradiação UV. Ainda foi obtido 80% de remoção de carbono orgânico total, cuja oxidação segue uma reação de pseudo-primeira ordem com constante de velocidade inicial de -0,040 mim-1 e uma eficiência de corrente de 51%. Os resultados são superiores á fotocatálise convencional nas mesmas condições sem a polarização do fotoanodo que leva a 65% de mineralização sob constante de velocidade de -0,024 mim-1.

Time‐Resolved Electron Spin Resonance Spectroscopy of Radicals Formed During Free Radical Polymerizations of Alkyl Acrylates

Time-resolved electron spin resonance (TR ESR) spectra allows direct observation of transient radicals (primary propagating radicals) obtained by the addition reaction of a diphenylphosphinoyl radical to acrylates. The addition rate constants (k(2) ) of the diphenylphosphinoyl radical to the acrylates (initiation rate constants) were determined by the monomer concentration dependence of the decay rate of the diphenylphosphinoyl radical. The value of k(2) was 1.9 × 10(7) s(-1) · M(-1) for the case of t-butyl acrylate, while the k(2) values of ethyl, n-butyl, 2-ethylhexyl, and dodecyl acrylates were about 1 × 10(7) s(-1) · M(-1) . A combination of steady state ESR and TR ESR provided information on the kinetics both of initiation and propagation processes in the radical polymerization of acrylates.

Kinetics of the production of chain-end groups and methanol from the depolymerization of cellulose during the ageing of paper/oil systems. Part 2: Thermally-upgraded insulating papers

In order to go further in demonstrating that methanol can be used as a universal cellulose degradation indicator in power transformers, the ageing study of standard wood kraft specimens in oil in the range of 60–130 °C (Gilbert et al. in Cellulose 16:327–338, 2009) has been extended to thermally-upgraded (TU) papers. The kinetic model that best tracks the ageing patterns was shown to be a function that can accelerate or decelerate the pseudo-zero kinetics by the adjustment of a free parameter. The results showed a non-negligible contribution of 1,4-β-glycosidic bond breaking in the crystalline regions suggesting that the degradation at this level is not necessary occurring through a quantum mode mechanism. The results also showed a significant error in the determination of the rate constants when obtained from isotherms of varying degree of depolymerization. In the case of TU papers, provided that there is a sufficient amount of stabilizers in the fibrous structure, not only could the self-catalyzing nature of the cellulose ageing process as well as the effect of an external supply of catalysts be lost but the chain-breaking could decrease to nearly zero for an undetermined period well before reaching the levelling-off degree of polymerization. The initial rate constants (k1o) for the depolymerization and methanol formation of these papers were found to be very near those of standard cellulose (giving about the same activation energy), which indicates that they are obtained from the ageing patterns well before the retardant action has fully taken place. The life extension of TU papers is achieved by a reduction with time of the frequency at which the bonds are ruptured. Moreover, the production of methanol and chain-end groups showed about the same value for the frequency factor, which introduces the possibility that the rate of production of CH3OH from chopped chains is much higher than the rate of depolymerization, so that the latter becomes the rate determining step of the overall reaction. On the other hand, the apparent yield of CH3OH molecules per scission is seen to increase substantially with the amount of stabilizers (from ~0.4 to 0.8 and to 1.4 for a paper containing 0 to 1.15 and to 3.9% (w/w) N2) and to a lesser extent, with the moisture in the specimens. However, these variations could either be attributed to a modification of the CH3OH paper/oil partitioning by the stabilizers and moisture in fibrous structure. Finally, pre-aged systems (130 °C for 168 h) conditioned at 20 °C for variable lengths of time provided further evidence that O2 is not necessarily involved in CH3OH production.

Adsorption Mechanism of Cr(VI) onto Coir Pith

ABSTRACT Reductive adsorption of Cr(VI) on coir pith (hereafter CP) was examined as a function of pH, ionic strength, and temperature. The CP contains 1.33 meq g− 1 phenolic, 0.43 meq g− 1 of lactonic, and 0.35 meq g− 1 carboxylic sites. Thus the CP surface is enriched with electron-donating oxygen functionalities. As evidenced by infrared (IR) spectroscopy, the Cr(VI) → Cr(III) conversion is facilitated by CP sites that are enriched with O─ O functional groups. The adsorption of reduced Cr(VI) was found to occur via C─ O─ functional groups first forming innersphere complexes with the CP surface, yielding keto (> C═ O) groups on the CP surface. The reductive adsorption of Cr(VI) was almost completed within 3 to 4 h, and it was dependent on pH and background ionic strength, yielding the highest monolayer coverage (9.56E-7 mol m− 2) at pH 3.7 in 0.1 M NaNO3. The ΓCr(III) followed the order with respect to the ionic strength: Γ0.1 M > Γ0.01 M > Γ0.001 M. The initial rate constant, k i , increased with temperature as k i 313 K > k i 303 K > k i 293 K > k i 283 K.

Chloroquine Transport inPlasmodium falciparum. 2. Analysis of PfCRT-Mediated Drug Transport Using Proteoliposomes and a Fluorescent Chloroquine Probe

Mutations in the PfCRT protein cause chloroquine resistance (CQR), and earlier studies from our laboratory using plasma membrane inside-out vesicles (ISOV) prepared from yeast expressing recombinant PfCRT [Zhang, H., et al. (2004) Biochemistry 43, 8290-8296] suggested that the putative transporter mediates downhill facilitated diffusion of charged chloroquine (CQ). However, more recent experiments with a fluorescent CQ probe (NBD-CQ) presented in the accompanying paper (DOI 10.1021/bi901034r ) indicated that the CQR phenotype in live parasites is associated with a reduced rate of ATP-dependent CQ uptake into the digestive vacuole (DV). An altered rate constant for uptake has multiple interpretations. To further investigate this phenomenon, PfCRT proteins found in chloroquine-sensitive (CQS) and CQR strains of Plasmodium falciparum were purified from yeast engineered to express "yeast optimized" pfcrt genes, reconstituted into proteoliposomes (PL), and efflux of NBD-CQ was measured from these PL. A membrane-impermeant quencher was used to distinguish intra-PL NBD-CQ from extra-PL NBD-CQ vs time as well as resolve initial rates and rate constants for efflux. Efflux was investigated at a range of NBD-CQ concentrations, in the presence vs absence of pH gradients (DeltapH) and transmembrane potentials (DeltaPsi). Explicit turnover numbers for apparent PfCRT-mediated transport were then calculated under these conditions. Our data are consistent with a model wherein PfCRT catalyzes electrochemically downhill diffusion of NBD-CQ out of the DV, in response to DeltaPsi or DeltapH, at a rate that can partially compete with the ATP-dependent uptake of NBD-CQ by CQS parasites described in the previous paper. These data allow us to propose a refined model for altered CQ accumulation in CQR malarial parasites.

Quantum wave packet study of the [formula omitted] reaction

The C ( 1 D ) + H 2 reaction was studied by the time-dependent quantum wave packet method. Coupled channel calculations have been carried out to get initial state-specified ( ν 0 = 0 , j 0 = 0 ) integral cross section and rate constant. All projection quantum numbers K were considered for each total angular momentum J value. At room temperature, the rate constant is reasonably in good agreement with the experimental value. Comparisons between the integral cross section and other theoretical results were also made. Initial state-specified ( ν 0 = 0 , j 0 = 1 , 2 ) rate constants were calculated by using the uniform J-shifting approximation. Only a slight increase for initial rotational excitations of H 2 was found.

Stability of Second Generation Grubbs’ Alkylidenes to Primary Amines: Formation of Novel Ruthenium‐Amine Complexes

AbstractThe stability of second generation Grubbs’ alkylidenes to primary amines relative to the first generation derivatives is investigated. For both Grubbs’ alkylidene derivatives, the tricyclohexylphosphine (PCy3) ligand is displaced by n‐butylamine and diethylenetriamine. However, while displacement of PCy3 in first generation Grubbs’ alkylidene derivatives results in decomposition of the catalyst, the N‐heterocyclic carbene (NHC) ligand in second generation derivatives is not displaced by primary amines present in up to 100 equivalents. The result is the formation of new stable ruthenium‐amine complexes. These complexes are characterized and their catalytic activity is evaluated in ring‐closing metathesis (RCM) and ring‐opening metathesis (ROMP) reactions. While the amine complexes evaluated were minimally active in RCM reactions, the ruthenium‐butylamine complex was significantly active in ROMP and exhibited an initiation rate constant that was at least an order of magnitude greater than that of the second generation Grubbs’ alkylidene from which it was synthesized.

Coupling Sequence-specific Recognition to DNA Modification

Enzymes that modify DNA are faced with significant challenges in specificity for both substrate binding and catalysis. We describe how single hydrogen bonds between M.HhaI, a DNA cytosine methyltransferase, and its DNA substrate regulate the positioning of a peptide loop which is approximately 28 A away. Stopped-flow fluorescence measurements of a tryptophan inserted into the loop provide real-time observations of conformational rearrangements. These long-range interactions that correlate with substrate binding and critically, enzyme turnover, will have broad application to enzyme specificity and drug design for this medically relevant class of enzymes.

Ester Hydrolysis by a Cyclodextrin Dimer Catalyst with a Tridentate N,N′,N′′‐Zinc Linking Group

A new beta-cyclodextrin dimer, 2,6-dimethylpyridine-bridged-bis(6-monoammonio-beta-cyclodextrin) (pyridyl BisCD, L), is synthesized. Its zinc complex (ZnL) is prepared, characterized, and applied as a catalyst for diester hydrolysis. The formation constant (log K(ML)=7.31+/-0.04) of the complex and deprotonation constant (pK(a1)=8.14+/-0.03, pK(a2)=9.24+/-0.01) of the coordinated water molecule were determined by a potentiometric pH titration at (25+/-0.1) degrees C, indicating a tridentate N,N',N''-zinc coordination. Hydrolysis kinetics of carboxylic acid esters were determined with bis(4-nitrophenyl)carbonate (BNPC) and 4-nitrophenyl acetate (NA) as the substrates. The resulting hydrolysis rate constants show that ZnL has a very high rate of catalysis for BNPC hydrolysis, yielding an 8.98x10(3)-fold rate enhancement over uncatalyzed hydrolysis at pH 7.00, compared to only a 71.76-fold rate enhancement for NA hydrolysis. Hydrolysis kinetics of phosphate esters catalyzed by ZnL are also investigated using bis(4-nitrophenyl)phosphate (BNPP) and disodium 4-nitrophenyl phosphate (NPP) as the substrates. The initial first-order rate constant of catalytic hydrolysis for BNPP was 1.29x10(-7) s(-1) at pH 8.5, 35 degrees C and 0.1 mM catalyst concentration, about 1600-fold acceleration over uncatalyzed hydrolysis. The pH dependence of the BNPP cleavage in aqueous buffer was shown as a sigmoidal curve with an inflection point around pH 8.25, which is nearly identical to the pK(a) value of the catalyst from the potentiometric titration. The k(BNPP) of BNPP hydrolysis promoted by ZnL is found to be 1.68x10(-3) M(-1) s(-1), higher than that of NPP, and comparatively higher than those promoted by its other tridentate N,N',N''-zinc analogues.

Efficient decolorization of azo dye Reactive Black B involving aromatic fragment degradation in buffered Co 2+/PMS oxidative processes with a ppb level dosage of Co 2+-catalyst

In order to generate powerful radicals as oxidizing species for the complete decolorization and degradation of azo dye Reactive Black B (RBB) at near neutral pH (pH 6), homogeneous activation of peroxymonosulfate (Oxone: PMS) by the trace Co 2+-catalysts was explored. We not only took advantage of the high oxidation–reduction potential of produced hydroxyl and sulfite radicals but also an opportunity to oxidize RBB to less complex compounds with extremely low dosages, especially the ppb level of the Co 2+-catalyst (stoichiometric ratio: [Co 2+] 0/[RBB] 0 = 1.7 × 10 −6–1.7 × 10 −5; [PMS] 0/[RBB] 0 = 8–32). Anion effects and pH effects were also carried out and discussed to simulate an actual application such as that of a textile waste stream. Both the degradations of RBB and its derivative aromatic fragments were illustrated successfully at UV–visable absorptions of 591 and 310 nm, respectively, and the possible relationships between them were also proposed and discussed, based on the experimental results. The RBB degradation in this Co 2+/PMS oxidative process successfully formulated a pseudo-first-order kinetic model at an isothermal condition of 25 °C with or without different anions present. The initial rate and rate constant were calculated under different comparative conditions, and the results indicate that the activity of both RBB decolorization and its degradation are not obviously dependent on the PMS concentration, but rather are related to the Co 2+ dosage.