The effect of carbon content on the rate of reduction of FeO in slag relevant to iron smelting

In the iron smelting, or bath smelting, process the tapped metal contains high amounts of sulfur and the slag contains high amounts of FeO, relative to blast furnace slag. After tapping, the FeO can be further reduced by carbon in the metal, which will also lead to better desulfurization. Although there have been many studies of the reaction of carbon in iron with FeO in slag, discrepancies exist with regards to the effect of carbon in iron on the rate of FeO reduction in slag, which is the subject of this study. Experiments were conducted at 1723 K, using a slag with basicity close to one with an FeO mass content of 5 %. The rate of reduction was measured using a pressure increase technique. For moderate and high sulfur contents, as in the case of iron smelting, the rate is primarily controlled by the dissociation of CO₂ on the surface of the molten iron. Furthermore, if the effect of carbon on sulfur is taken into account, for the range of carbon mass contents of 2 to 4.5 %, there is no effect of the carbon level on the rate of FeO reduction. At low sulfur contents it was found that there is considerable slag foaming, which inhibits mass transfer of FeO in the slag, and significantly reduces the rate. Even when there is no slag foaming at low sulfur contents, mass transfer of FeO in the slag can influence the rate of FeO reduction.     

钒钛磁铁矿煤基直接还原试验

 为探明钒钛磁铁矿直接还原过程及其影响因素,研究了不同还原温度、不同还原时间、不同配碳比对钒钛磁铁矿含碳团块直接还原过程的影响,并通过XRD分析方法对还原机理进行了分析。研究结果表明,在一定条件下,直接还原团块金属化率随温度升高而升高,但还原温度超过1 200 ℃后,金属化率增幅逐渐减少,这是由于还原温度高于1 200 ℃后,金属化团块内铁氧化物的还原逐渐趋于平缓,而铁钛化合物的还原较为缓慢;团块金属化率随反应时间的延长和配碳比的升高均呈现了先升高后降低的趋势,这主要是由于反应时间过长使得金属化团块发生了再氧化及煤粉配入量过大导致带入灰分较多,在一定程度上阻碍了还原反应的顺利进行,从而导致金属化率降低。     

Enhanced dissociation of HLA-DR-bound peptides in the presence of HLA-DM

Human leukocyte antigen (HLA)-DM is a critical participant in antigen presentation that catalyzes the release of class II-associated invariant chain-derived peptides (CLIP) from newly synthesized class II histocompatibility molecules, freeing the peptide-binding site for acquisition of antigenic peptides. The mechanism for the selective release of CLIP but not other peptides is unknown. DM was found to enhance the rate of peptide dissociation to an extent directly proportional to the intrinsic rate of peptide dissociation from HLA-DR, regardless of peptide sequence. Thus, CLIP is rapidly released in the presence of DM, because its intrinsic rate of dissociation is relatively high. In antigen presentation, DM has the potential to markedly enhance the rate of peptide exchange, favoring the presentation of peptides with slower intrinsic rates of dissociation.     

铁矿石还原过程速率探讨

本文定义了还原反应速率的计算式，依据矿石失重实验数据可计算反应速率的大小及其变化关系，可分析矿石还原过程速率的限制性环节。     

Tolbutamide causes open channel blockade of cystic fibrosis transmembrane conductance regulator Cl- channels

Cystic fibrosis transmembrane conductance regulator (CFTR) is an epithelial Cl- channel that is regulated by protein kinase A and cytosolic nucleotides. Previously, Sheppard and Welsh reported that the sulfonylureas glibenclamide and tolbutamide reduced CFTR whole cell currents. The aim of this study was to quantify the effects of tolbutamide on CFTR gating in excised membrane patches containing multiple channels. We chose tolbutamide because weak (i.e., fast-type) open channel blockers introduce brief events into multichannel recordings that can be readily quantified by current fluctuation analysis. Inspection of current records revealed that the addition of tolbutamide reduced the apparent single-channel current amplitude and increased the open-channel noise, as expected for a fast-type open channel blocker. The apparent decrease in unitary current amplitude provides a measure of open probability within a burst (P0 Burst), and the resulting concentration-response relationship was described by a simple Michaelis-Menten inhibition function. The concentration of tolbutamide causing a 50% reduction of Po Burst (540 +/- 20 microM) was similar to the concentration producing a 50% inhibition of short-circuit current across T84 colonic epithelial cell monolayers (400 +/- 20 microM). Changes in CFTR gating were then quantified by analyzing current fluctuations. Tolbutamide caused a high-frequency Lorentzian (corner frequency, fc > 300 Hz) to appear in the power density spectrum. The fc of this Lorentzian component increased as a linear function of tolbutamide concentration, as expected for a pseudo-first-order open-blocked mechanism and yielded estimates of the on rate (koff = 2.8 +/- 0.3 microM-1 s-1), the off rate (kon = 1210 +/- 225 s-1), and the dissociation constant (KD = 430 +/- 80 microM). Based on these observations, we propose that there is a bimolecular interaction between tolbutamide and CFTR, causing open channel blockade.     

The rate of absorption of hydrogen into iron and of nitrogen into Fe-Cr and Fe-Ni-Cr alloys containing sulfur

The rate of absorption of hydrogen into liquid iron and of nitrogen into liquid Fe-Cr alloys containing various levels of sulfur was measured by using a constant-volume Sieverts apparatus employing a sensitive pressure transducer. The rate for the absorption of hydrogen was measured by using H2 containing a small amount of H₂S(<0.2 pct) such that the activity of sulfur on the surface of the melt was the same as in the bulk metal. The hydrogen-absorption rate for Fe-S melts containing up to 0.72 pet sulfur was virtually independent of sulfur content and controlled by liquid-phase mass transfer. The liquidphase mass-transfer coefficient for hydrogen in liquid iron, calculated from the results, was comparable to that for nitrogen transfer in liquid iron. The rate of absorption of nitrogen into Fe-Cr melts with low-sulfur contents was controlled by liquid-phase mass transfer. For melts containing significant amounts of sulfur it was controlled by both mass transfer and the chemical rate of the dissociation of nitrogen on the surface in series. Equations were developed to calculate the chemical rate from the measured rate, correcting for mass transfer. The chemical rate decreased with increasing sulfur content as expected, because sulfur is strongly adsorbed on the surface and increased with chromium content at constant sulfur activity, possibly because available Cr sites promote nitrogen dissociation. Formerly with United States Steel Corporation, Monroeville, PA     

Participation of ADP dissociation in the rate-determining step in cAMP-dependent protein kinase

Pre-steady-state kinetic analyses of the catalytic subunit of cAMP-dependent protein kinase showed that the rate constant for phosphoryl transfer is fast and either the release of one or both of the products or a conformational change controls turnover [Grant, B., & Adams, J. A. (1996) Biochemistry 35, 2022-2029]. To determine which step or steps control turnover in the wild-type enzyme, we used a catalytic trapping technique to measure directly the dissociation rate constant for ADP. The phosphorylation of two peptide substrates, LRRASLG and GRTGRRNSI, was monitored using a rapid quench flow technique under conditions where saturating concentrations of ADP were preequilibrated with the enzyme before excess ATP and one of the substrates were added to trap the free enzyme and to start the phosphorylation reaction. Under ADP preequilibration conditions, no 'burst' phase was observed, and although the rate of linear, steady-state turnover was unaffected, the net production of phosphopeptide lagged behind the non-preequilibrated control. This phenomenon occurs due to the slow release of the product, and kinetic modeling suggests that this effect can be explained if the dissociation rate constant for ADP is 24 s-1 and solely limits turnover (kcat = 23 s-1) for the phosphorylation of LRRASLG. Using GRTGRRNSI, the dissociation rate constant for ADP is 35 s-1 and limits turnover (kcat = 29 s-1) if the reaction is initiated by the addition of enzyme. Under preequilibration conditions with either ATP or GRTGRRNSI, turnover is approximately 50% lower, suggesting that ADP release may partially control this parameter. This preequilibration effect can be explained by slowly interconverting enzyme forms with specific peptide-induced turnover properties. These studies indicate that ADP release is an essential rate-limiting component for turnover but also suggests that other factors contribute subtly when the structure of the substrate is altered.     

Evaluation of Dissociation Throughout the Lifespan.

In the past 20 years, the study of dissociation has flourished partly because of the research on the links between traumatic events and dissociation. Epidemiological studies have shown that dissociative symptoms and disorders are not uncommon. The nonspecialist in this area needs a guide to the extensive literature on the evaluation of dissociation across the lifespan to choose the most appropriate form of evaluation. The authors provide summaries of various types of assessment for dissociation in infants, children, teens, and adults. The techniques they review include structured interviews, specialized questionnaires, and scales on more general instruments, along with their psychometric properties. A good evaluation of dissociation can guide diagnosis, help focus treatment, and provide a measure of treatment efficacy. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Protein folding: how the mechanism of GroEL action is defined by kinetics

We propose a mechanism for the role of the bacterial chaperonin GroEL in folding proteins. The principal assumptions of the mechanism are (i) that many unfolded proteins bind to GroEL because GroEL preferentially binds small unstructured regions of the substrate protein, (ii) that substrate protein within the cavity of GroEL folds by the same kinetic mechanism and rate processes as in bulk solution, (iii) that stable or transient complexes with GroEL during the folding process are defined by a kinetic partitioning between formation and dissociation of the complex and the rate of folding and unfolding of the protein, and (iv) that dissociation from the complex in early stages of folding may lead to aggregation but dissociation at a late stage leads to correct folding. The experimental conditions for refolding may play a role in defining the function of GroEL in the folding pathway. We propose that the role of GroES and MgATP, either binding or hydrolysis, is to regulate the association and dissociation processes rather than affecting the rate of folding.     

US-guided hydrostatic reduction of intussusception in children

Over a period of 3 3/4 years, hydrostatic reduction of ileocolic intussusception was performed under sonographic guidance in 47 cases (a total of 41 consecutive patients). The enema consisted of a mixture of isotonic electrolyte solution and water-soluble contrast medium (9:1 ratio) and was given at a hydrostatic pressure of 80-100 cm water. Reduction was successful in 83% of cases (n = 39). Even initially remaining ileo-ileal intussusception could finally be reduced in two cases. No complications were observed. Since, in comparison with other conservative methods of reduction, the success rate was not substantially worse (versus that of pneumatic reduction) or was even higher (versus that of barium enema reduction), the method described can be recommended for wider use because of the substantial reduction in radiation exposure.     

Analysis of isomeric mixtures using blackbody infrared radiative dissociation: determining isomeric purity and obtaining individual tandem mass spectra simultaneously

A new method that makes possible, for the first time, simultaneous acquisition of individual dissociation mass spectra of isomeric ions in mixtures is presented. This method exploits the exquisite sensitivity of blackbody infrared radiative dissociation kinetics to minor differences in ion structure. Instead of separating precursor ions based on mass (isomers have identical mass), fragment ions are related to their original precursor ions on the basis of rate constants for dissociation. Mixtures of the peptide isomers des-R1 and des-R9 bradykinin are dissociated simultaneously at several temperatures. By fitting the kinetic data to double-exponential functions, the dissociation rate constant and abundance of each isomer in the mixture are obtained. To overcome the difficulty of fitting double-exponential functions, a novel global analysis method is used in which several dissociation data sets collected at different temperatures are simultaneously fit. The kinetic data measured at multiple temperatures are modeled with the preexponentials (corresponding to the abundance of each isomer) as "global" parameters which are constant for all data sets and the exponentials (rate constants) as "local" variables which differ for each data set. The use of global parameters significantly improves the accuracy with which abundances and dissociation rate constants of each individual compound can be obtained from the mixture data. Fragment ions produced from a mixture of these two isomers are related back to their respective precursor ions from the kinetic data. Thus, not only can the composition of the isomeric mixture be determined but an individual tandem mass spectrum of each component in the mixture can be obtained.     

The importance of convective mass transfer in the reduction of hematite

The relative importance of transport phenomena, as opposed to chemical phenomena, in controlling the kinetics of hematite reduction has been debated for a long time. Recent measurements of gaseous diffusion coefficients in the porous iron and intermediate oxide layers produced by the reduction have shown that gaseous diffusion plays an increasingly important role, especially towards the end of the reaction. Convective mass transfer, however, is still assumed to play a negligible role, principally because of the way in which the reduction rate of hematite particles varies with the gas flow rate, and with the parti-cle diameter. The established theories of convective mass transfer are used in this paper to show that the observed variations would occur whatever contribution convective mass transfer was making to controlling the reduction rate. The observed variations, therefore, give no indication as to the relative importance of convective mass transfer. This paper then, makes a quantitative comparison between the mass transfer rates necessary to sus-tain the reaction rates observed in recent hematite reduction experiments and the rates predicted by the established theories of mass transfer. This comparison shows that con-vective mass transfer can play a major role in controlling the reduction rate, although the relative magnitude of its contribution varies with particle size, and with reduction temperature.     

Ferredoxin reduction by photosystem I from Synechocystis sp. PCC 6803: toward an understanding of the respective roles of subunits PsaD and PsaE in ferredoxin binding

The process of ferredoxin reduction by photosystem I has been extensively investigated by flash-absorption spectroscopy in psaD and psaE deleted mutants from Synechocystis sp. PCC 6803. In both mutants, the dissociation constant for the photosystem I/ferredoxin complex at pH 8 is considerably increased as compared to the wild type: approximately 25- and 100-fold increases are found for PsaD-less and PsaE-less photosystem I, respectively. However, at high ferredoxin concentrations, submicrosecond and microsecond kinetics of electron transfer similar to that observed in the wild type are present in both mutants. The presence of these fast kinetic components indicates that the relative positions of ferredoxin and of the terminal photosystem I acceptor are not significantly disturbed by the absence of either PsaD or PsaE. The second-order rate constant of ferredoxin reduction is lowered 10- and 2-fold for PsaD-less and PsaE-less photosystem I, respectively. Assuming a simple binding equilibrium between photosystem I and ferredoxin, PsaD appears to be important for the guiding of ferredoxin to its binding site (main effect on the association rate) whereas PsaE seems to control the photosystem I/ferredoxin complex lifetime (main effect on the dissociation rate). The properties of electron transfer from photosystem I to ferredoxin were also studied at pH 5. 8. In the psaE deleted mutant as in the wild type, the change of pH from 8 to 5.8 induces a 10-fold increase in affinity of ferredoxin for photosystem I. In the absence of PsaD, this pH effect is not observed, in favor of this subunit being mostly responsible for the low pH increased affinity.     

The importance of convective mass transfer in the reduction of hematite

The relative importance of transport phenomena, as opposed to chemical phenomena, in controlling the kinetics of hematite reduction has been debated for a long time. Recent measurements of gaseous diffusion coefficients in the porous iron and intermediate oxide layers produced by the reduction have shown that gaseous diffusion plays an increasingly important role, especially towards the end of the reaction. Convective mass transfer, however, is still assumed to play a negligible role, principally because of the way in which the reduction rate of hematite particles varies with the gas flow rate, and with the particle diameter. The established theories of convective mass transfer are used in this paper to show that the observed variations would occur whatever contribution convective mass transfer was making to controlling the reduction rate. The observed variations, therefore, give no indication as to the relative importance of convective mass transfer. This paper then, makes a quantitative comparison between the mass transfer rates necessary to sustain the reaction rates observed in recent hematite reduction experiments and the rates predicted by the established theories of mass transfer. This comparison shows that convective mass transfer can play a major role in controlling the reduction rate, although the relative magnitude of its contribution varies with particle size, and with reduction temperature.     

Recollection and familiarity deficits in amnesia: Convergence of remember-know, process dissociation, and receiver operating characteristic data.

Previous studies using the process dissociation and the remember–know procedures led to conflicting conclusions regarding the effects of anterograde amnesia on recollection and familiarity. We argue that these apparent contradictions arose because different models were used to interpret the results and because differences in false-alarm rates between groups biased the estimates provided by those models. A reanalysis of those studies with a dual-process signal-detection model that incorporates response bias revealed that amnesia led to a pronounced reduction in recollection and smaller but consistent reduction in familiarity. To test the assumptions of the model and to further assess recognition deficits in amnesics, we examined receiver operating characteristics (ROCs) in amnesics and controls. The ROCs of the controls were curved and asymmetrical, whereas those of the amnesics were curved and symmetrical. The results supported the predictions of the model and indicated that amnesia was associated with deficits in both recollection and familiarity. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

拉丝断面压缩率对10B30钢球化退火组织及力学性能的影响

研究了拉丝断面压缩率(5%～35%)对Φ9.67～11.69 mm 10B30钢丝(/%:0.28～0.34C, 0.0005～0.0030B)球化退火组织及力学性能的影响。结果表明：随着球化退火前拉丝断面压缩率的增加,球化退火组织级别提高,抗拉强度降低,断面收缩率提高,这是因为拉丝促进了球化退火过程中的自发球化和碳化物的ostwald熟化;当拉丝断面压缩率达到25%以上,球化组织和相应的抗拉强度和断面收缩率趋于稳定;实际生产中,退火前拉丝断面压缩率不应低于25%。     

Quaternary structure regulates hemin dissociation from human hemoglobin

Rate constants for hemin dissociation from the alpha and beta subunits of native and recombinant human hemoglobins were measured as a function of protein concentration at pH 7.0, 37 degrees C, using H64Y/V68F apomyoglobin as a hemin acceptor reagent. Hemin dissociation rates were also measured for native isolated alpha and beta chains and for recombinant hemoglobin tetramers stabilized by alpha subunit fusion. The rate constant for hemin dissociation from beta subunits in native hemoglobin increases from 1.5 h-1 in tetramers at high protein concentration to 15 h-1 in dimers at low concentrations. The rate of hemin dissociation from alpha subunits in native hemoglobin is significantly smaller (0.3-0.6 h-1) and shows little dependence on protein concentration. Recombinant hemoglobins containing a fused di-alpha subunit remain tetrameric under all concentrations and show rates of hemin loss similar to those observed for wild-type and native hemoglobin at high protein concentration. Rates of hemin dissociation from monomeric alpha and beta chains are much greater, 12 and 40 h-1, respectively, at pH 7, 37 degrees C. Aggregation of monomers to form alpha1beta1 dimers greatly stabilizes bound hemin in alpha chains, decreasing its rate of hemin loss approximately 20-fold. In contrast, dimer formation has little stabilizing effect on hemin binding to beta subunits. A significant reduction in the rate of hemin loss from beta subunits does occur after formation of the alpha1beta2 interface in tetrameric hemoglobin. These results suggest that native human hemoglobin may have evolved to lose heme rapidly after red cell lysis, allowing the prosthetic group to be removed by serum albumin and apohemopexin.     

Binding kinetics of monoclonal antibody using antigen-beta-galactosidase hybrid protein: application to measurement of peptide antigenicity

A simple method for determination of binding kinetics of a solid-phase antibody using antigen-beta-galactosidase hybrid protein was evaluated. To minimize conformational change of the antigen binding site of the antibody when directly binding to a microtiter plate, the microtiter plate was precoated with protein A. The binding and free antigen concentrations were directly obtained from the beta-galactosidase activity. This method can be used for analyses of the equilibrium dissociation constant (KD), and the association (Kass) and dissociation (Kdiss) rate constants. Peptide antigenicity was also analyzed by competitive ELISA using this method. Since both antigen-beta-galactosidase and the peptide used are localized in the fluid-phase, the proper affinity constant (KA) of the peptide can be estimated from the KD value of the antigen-beta-galactosidase-antibody interaction, and from the IC50 value of the peptide.     

Catalytic activity of thermolysin under extremes of pressure and temperature: modulation by metal ions

The catalytic activity of thermolysin (TL), a Zn-dependent neutral protease from Bacillus thermoproteolyticus, has been studied over a wide interval of pressures (1 bar to 4 kbar) and temperatures (20 degreesC to 80 degreesC) by monitoring hydrolysis of a low-molecular-mass substrate, 3-(2-furylacryloyl)-glycyl-L-leucine amide. This reaction shows a very large negative value for the activation volume and, because of that, simultaneous increase in temperature and pressure leads to a significant (up to 40-fold) acceleration of the reaction. At pressures higher than 2-2.5 kbar, the reaction rate starts to decrease due to disactivation of TL. This disactivation is explained in part by pressure-promoted dissociation of zinc ion from the active site and can be inhibited by adding exogenous zinc. Thus, this thermostable protease does not specifically show a higher stability at high pressure in comparison with small mesophilic proteases.     

The rate of absorption of nitrogen into liquid iron containing oxygen and sulfur

The rate of nitrogen absorption into and desorption from liquid iron containing sulfur and/or oxygen was measured by employing a constant-volume technique with a highly sensitive pressure transducer. Critical evaluation of the results demonstrated conclusively that the chemical rate at high oxygen or sulfur contents is second order with respect to nitrogen content in the metal and probably controlled by the dissociation of the nitrogen molecule on the surface. The effect of sulfur on the rate is complex because of the influence of 1) liquid-phase mass transfer at low sulfur contents, 2) the chemical rate on vacant iron sites at intermediate sulfur contents, and 3) the rate on the adsorbed sulfur layer or the limiting rate at high sulfur contents. However, at intermediate concentrations the limiting case for the adsorption isotherm for sulfur is adhered to and the rate is inversely proportional to the sulfur concentration. For Fe-O melts the rate is inversely proportional to the oxygen content except at low oxygen levels where mass transfer affects the rate. The rate for Fe-S-O melts can be calculated reasonably well from the results for the Fe-S and Fe-0 alloys, assuming that oxygen does not effect the adsorption of sulfur andvice versa and that there is nearly complete coverage of the surface with oxygen and sulfur atoms.