Temperature-induced changes in blood acid-base status: Donnan rCl and red cell volume

1976 ◽  
Vol 40 (5) ◽  
pp. 762-767 ◽  
Author(s):  
R. B. Reeves
Keyword(s):  
Variable Temperature ◽  
Chloride Ion ◽  
Chloride Ions ◽  
Red Cell ◽  
Co2 Partial Pressure ◽  
Acid Base Status ◽  
Ph Range ◽  
Induced Changes ◽  
Donnan Ratio ◽  
Human Red Cells

The Donnan ratio for chloride ion (rCl) was determined for human red cells in plasma utilizing 36Cl. The effect of altered PCO2 and pH on rCl was followed in two ways. CO2 partial pressure was varied (1–1.5% CO2 in O2; pH range 7.1–7.9) at 37.5 degrees C (isothermal); PCO2 and pH were also changed by altering temperature (range 5–45 degrees C) at constant CO2 content (temperature induced). At pH 7.4 and 37.5 degrees C, rCl was 0.631 +/- 0.0269 (SE, N = 5); isothermal drcl/dpH = -0.306 +/- 0.0234. When measured under conditions of variable temperature at constant CO2 content (pH range 7.3–7.9), drcl/dpH = .018 +/- 0.0232, significantly different from isothermal response (P less than 0.001). Hematocrit (H) changes with pH for conditions of initial H(7.4) of 0.45, under these conditions were also determined: isothermal dH/dpH = -0.031 +/- 0.0019; temperature induced, -0.004 +/- 0.0009. Temperature change alone at constant carbon dioxide content produces no significant change in distribution of chloride ions or water between erythrocyte and plasma compartments.

Rate of bicarbonate-chloride exchange in human red cells at 37 degrees C

1976 ◽  
Vol 40 (5) ◽  
pp. 707-714 ◽  
Author(s):  
R. A. Klocke
Keyword(s):  
Continuous Flow ◽  
Co2 Concentration ◽  
Carbonic Anhydrase Activity ◽  
Chloride Ions ◽  
Red Cell ◽  
Chloride Permeability ◽  
Red Cell Membrane ◽  
Chloride Exchange ◽  
Rapid Reaction ◽  
Human Red Cells

The rate of exchange of bicarbonate and chloride ions across the red cell membrane was studied in a continuous flow rapid reaction apparatus at 37 degrees C. A transmembrane gradient both ions was produced by mixture of cells suspended in a solution of one ion with an isosmotic solution of the other ion. Carbonic anhydrase activity was inhibited by acetazolamide to prevent changes in CO2 concentration during the experiments. Chloride and bicarbonate efflux from cells were studied in separate experiments at each experimental pH. Using a least squares technique, values of chloride and bicarbonate permeabilities were fitted to each pair of independent experiments. Chloride permeability averaged 1.1 (+/- 0.2 SD) X 10–4 cm/s and was not affected by change in pH. Recovered bicarbonate permeabilities varied widely, always remaining at least fivefold greater than chloride permeability. While bicarbonate permeability could not be accurately characterized, it appears to be greater than chloride permeability. Analysis of CO2 transfer with the estimated permeabilities indicates that the bicarbonate-chloride exchange by itself probably does not limit CO2 transfer.

The chemical stability of mendipite, diaboleïte, chloroxiphite, and cumengéite, and their relationships to other secondary lead(II) minerals

1980 ◽  
Vol 43 (331) ◽  
pp. 901-904 ◽  
Author(s):  
D. Alun Humphreys ◽  
John H. Thomas ◽  
Peter A. Williams ◽  
Robert F. Symes
Keyword(s):  
Chloride Ion ◽  
Stability Diagram ◽  
Chloride Ions ◽  
Ion Concentration ◽  
Stability Field ◽  
Cupric Ion ◽  
Free Energy Of Formation ◽  
High Concentrations ◽  
The Stability ◽  
Ph Range

SummaryThe chemical stabilities of mendipite, Pb3O2Cl2, diaboleïte, Pb2CuCl2(OH)4, chloroxiphite, Pb3CuCl2O2(OH)2, and cumengéite, Pb19Cu24Cl42 (OH)44, have been determined in aqueous solution at 298.2 K. Values of standard Gibbs free energy of formation, ΔGf°, for the four minerals are −740, −1160, −1129, and −15163±20 kJ mol−1 respectively. These values have been used to construct the stability diagram shown in fig. I which illustrates their relationships to each other and to the minerals cotunnite, PbCl2, paralaurionite, PbOHCl, and litharge, PbO. This diagram shows that mendipite occupies a large stability field and should readily form from cold, aqueous, mineralizing solutions containing variable amounts of lead and chloride ions, and over a broad pH range. The formation of paralaurionite and of cotunnite requires a considerable increase in chloride ion concentration, although paralaurionite can crystallize under much less extreme conditions than cotunnite. The encroachment of the copper minerals on to the stability fields of those mineral phases containing lead(II) only is significant even at very low relative activities of cupric ion. Chloroxiphite has a large stability field, and at given concentrations of cupric ion, diaboleïte is stable at relatively high aCl−. Cumengéite will only form at high concentrations of chloride ion.

scholarly journals Experimental Study and Simulation Calculation of the Chloride Resistance of Concrete under Multiple Factors

2021 ◽  
Vol 11 (12) ◽  
pp. 5322
Author(s):  
Yang Ding ◽  
Tong-Lin Yang ◽  
Hui Liu ◽  
Zhen Han ◽  
Shuang-Xi Zhou ◽  
...  
Keyword(s):  
Hydrostatic Pressure ◽  
Penetration Depth ◽  
Chloride Ion ◽  
Cementitious Materials ◽  
Chloride Ions ◽  
Finite Element Software ◽  
Chloride Resistance ◽  
Simulation Calculation ◽  
Marine Concrete ◽  
Resistance Performance

Cement is widely used in marine concrete, and its resistance to chloride ion corrosion has been widely considered. In this paper, based on a laboratory test, the influence of different hydrostatic pressures, coarse aggregate contents and w/c ratios on the chloride resistance performance is analyzed. Based on COMSOL finite element software, a two-dimensional cementitious materials model is established, and the simulation results are compared with the experimental results. The results show that the penetration depth of chloride ions in cement increases with the increase of the w/c ratio. Under the hydrostatic pressure of 0 MPa, when the w/c ratio is 0.35, the penetration depth of chloride ions is 7.4 mm, and the simulation result is 8.0 mm. When the w/c ratio is 0.45, the penetration depth of chloride ions is 9.3 mm, and the simulation result is 9.9 mm. When the w/c ratio is 0.55, the penetration depth of chloride ions is 12.9 mm, and the simulation result is 12.1 mm. Under different hydrostatic pressures, the penetration depth of chloride ions obviously changes, and with the increase in hydrostatic pressure, the penetration depth of chloride ions deepens. Under the w/c ratio of 0.35, when the hydrostatic pressure is 0.5 MPa, the penetration depth of chloride ions is 11.3 mm, and the simulation result is 12.1 mm. When the hydrostatic pressure is 1.0 MPa, the penetration depth of chloride ions is 16.2 mm, and the simulation result is 17.5 mm.

scholarly journals Broadband dielectric spectroscopy for monitoring temperature-dependent chloride ion motion in BiOCl plates

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Adrian Radoń ◽  
Dariusz Łukowiec ◽  
Patryk Włodarczyk
Keyword(s):  
Electrical Conductivity ◽  
Dielectric Spectroscopy ◽  
Low Frequency ◽  
Chloride Ion ◽  
Ion Source ◽  
Chloride Ions ◽  
Ion Concentration ◽  
Broadband Dielectric Spectroscopy ◽  
Free Chloride ◽  
Structure Rebuilding

AbstractThe dielectric properties and electrical conduction mechanism of bismuth oxychloride (BiOCl) plates synthesized using chloramine-T as the chloride ion source were investigated. Thermally-activated structure rebuilding was monitored using broadband dielectric spectroscopy, which showed that the onset temperature of this process was 283 K. This rebuilding was related to the introduction of free chloride ions into [Bi2O2]2+ layers and their growth, which increased the intensity of the (101) diffraction peak. The electrical conductivity and dielectric permittivity were related to the movement of chloride ions between plates (in the low-frequency region), the interplanar motion of Cl− ions at higher frequencies, vibrations of these ions, and charge carrier hopping at frequencies above 10 kHz. The influence of the free chloride ion concentration on the electrical conductivity was also described. Structure rebuilding was associated with a lower concentration of free chloride ions, which significantly decreased the conductivity. According to the analysis, the BiOCl plate conductivity was related to the movement of Cl− ions, not electrons.

scholarly journals Layered Double Hydroxides Precursor as Chloride Inhibitor: Synthesis, Characterization, Assessment of Chloride Adsorption Performance

Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2537 ◽  
Author(s):  
Lin Chi ◽  
Zheng Wang ◽  
Youfang Zhou ◽  
Shuang Lu ◽  
Yan Yao
Keyword(s):  
Removal Rate ◽  
Chloride Ion ◽  
Cementitious Materials ◽  
Chloride Ions ◽  
Ion Removal ◽  
Hydraulic Concrete ◽  
Adsorption Behaviors ◽  
The Stability ◽  
Inhibition Performance ◽  
Double Hydroxides

In this study, the chloride adsorption behaviors of CaAl-Cl LDH precursors with various Ca:Al ratios were investigated. The optimal chloride ion removal rate was 87.06% due to the formation of hydrocalumite. The chloride adsorption products of CaAl-Cl LDH precursors were further characterized by X-ray diffraction analysis and atomic structure analysis, the adsorption mechanism was considered to be co-precipitate process. The chloride adsorption behaviors of cementitious materials blended with CaAl-Cl LDH precursors were further investigated. Leaching test according to Test Code for Hydraulic Concrete (SL352-2006) was performed to testify the stability of chloride ions in the mortar. The results show that more than 98.3% chloride ions were immobilized in cement mortar blended with CaAl-Cl LDH precursor and cannot be easily released again. The inhibition performance of steel in the electrolytes with/without CaAl LDH precursor was investigated by using electrochemical measurements. The results indicate that CaAl LDH precursor can effectively protect the passive film on steel surface by chloride adsorption. Considering the high anion exchange capacities of the LDHs, synthesized chloride adsorbent precursor can be applied as new inhibitors blended in cementitious materials to prevent the chloride-induced deterioration. Moreover, the application of chloride adsorption on CaAl-Cl LDH could also be of interest for the application of seawater blended concrete.

scholarly journals Kinetics and stoichiometry of Na-dependent Li transport in human red blood cells.

1978 ◽  
Vol 72 (2) ◽  
pp. 249-265 ◽  
Author(s):  
B Sarkadi ◽  
J K Alifimoff ◽  
R B Gunn ◽  
D C Tosteson
Keyword(s):  
Transport System ◽  
Red Cells ◽  
Normal Male ◽  
Red Cell ◽  
Red Cell Membrane ◽  
Human Red Blood Cells ◽  
Na Efflux ◽  
Tightly Coupled ◽  
Male Subjects ◽  
Human Red Cells

This paper describes the kinetics and stoichiometry of a tightly coupled Na-Li exchange transport system in human red cells. The system is inhibited by phloretin and furosemide but not by ouabain. Li influx by this system increases and saturates with increasing concentrations of external Li and internal Na and is inhibited competitively by external Na. Comparable functions relate Li efflux and Na efflux to internal and external Li and Na concentrations. Analysis of these relations yields the following values for the ion concentrations required to half-maximally activate the transport system: internal Na and Li 9.0 and 0.5 mM, respectively, external Na and Li 25 and 1.5 mM, respectively. The system performs a 1:1 exchange of Na and Li moving in opposite directions across the red cell membrane. We found no evidence for a simultaneous transport of more than one Na and Li by the system. The maximum transport rate of Na-dependent Li transport varied between 0.1 and 0.37 mmol/(liter of cells X h) in the red cells of the five normal male subjects studied. No significant variations between individual subjects were observed for bicarbonate-stimulated Li transport and for the residual Li fluxes which occur in the absence of bicarbonate and in the presence of ouabain plus phloretin.

GABA responses in rat dentate granule neurons are mediated by chloride

1988 ◽  
Vol 66 (5) ◽  
pp. 637-642 ◽  
Author(s):  
Timothy J. Blaxter ◽  
Peter L. Carlen
Keyword(s):  
Granule Cells ◽  
Hippocampal Slices ◽  
Reversal Potential ◽  
Chloride Ion ◽  
Chloride Ions ◽  
Ion Concentration ◽  
Aminobutyric Acid ◽  
Granule Neurons ◽  
Nernst Equation ◽  
Central Neurons

The dendrites of granule cells in hippocampal slices responded to γ-aminobutyric acid (GABA) with a depolarization. The response was blocked by picrotoxin in a noncompetitive manner. Reductions in the extracellular chloride ion concentration changed the reversal potential of the response by an amount predicted from the Nernst equation for chloride ion. Chloride-dependent hyperpolarizing responses were sometimes also found in the cell body of the granule cells. Since the reversal potential followed that predicted from the Nernst equation for chloride, we conclude that the response was mediated by chloride ions alone with no contribution from other ions. This has not previously been shown for the depolarizing response to GABA in central neurons.

scholarly journals AERVA LANATA LEAF EXTRACT AS A CORROSION INHIBITOR FOR CARBON STEEL IN CHLORIDE ENVIRONMENT

2018 ◽  
Vol 6 (11) ◽  
pp. 153-162
Author(s):  
Rajesh V. ◽  
E. U. B. Reddi ◽  
T. Byragi Reddy ◽  
Ch. Durga Prasad ◽  
B. Prasanna Kumar
Keyword(s):  
Carbon Steel ◽  
Corrosion Inhibitor ◽  
Leaf Extract ◽  
Inhibition Efficiency ◽  
Aggressive Medium ◽  
Chloride Ions ◽  
Aqueous Environment ◽  
Aerva Lanata ◽  
Ph Range ◽  
Chloride Environment

The present study was initiated with an objective of investigating a plant extract as an effective corrosion inhibitor useful for protection of carbon steel in aqueous environment containing chloride ions. For this purpose, the leaf extract of the plant ‘Aerva lanata’ belonging to Amaranthaceae family of genus Aerva was chosen. The required optimum concentration of the extract for an effective inhibition was found to be 5 %, resulting in the inhibition efficiency of 95 % against corrosion of carbon steel in 200 ppm of NaCl solution. The extract introduced as a corrosion inhibitor was found to be effective in the pH range from 4.0 to 9.0. The extract could retain its inhibition efficiency for about an immersion period of 60 days and also up to a temperature of 333 K. The 5 % extract was found to control corrosion of carbon steel in highly aggressive medium containing 300 ppm of NaCl also. In order to maintain the protective nature, the required concentration of the extract was 2 %. From these studies, it was inferred that the Aerva lanata leaf extract exhibits good inhibitive properties for carbon steel in aqueous environment in wide ranges of pH, temperature and aggressiveness of medium.

scholarly journals Faropenem Transport across the Renal Epithelial Luminal Membrane via Inorganic Phosphate Transporter Npt1

2000 ◽  
Vol 44 (3) ◽  
pp. 574-577 ◽  
Author(s):  
Hiroshi Uchino ◽  
Ikumi Tamai ◽  
Hikaru Yabuuchi ◽  
Kayoko China ◽  
Ken-ichi Miyamoto ◽  
...  
Keyword(s):  
Inorganic Phosphate ◽  
Expression System ◽  
Mevalonic Acid ◽  
Chloride Ion ◽  
Chloride Ions ◽  
Phosphate Transporter ◽  
Disulfonic Acid ◽  
Renal Secretion ◽  
Luminal Membrane ◽  
Anionic Drugs

ABSTRACT We previously showed that the mouse inorganic phosphate transporter Npt1 operates in the hepatic sinusoidal membrane transport of anionic drugs such as benzylpenicillin and mevalonic acid. In the present study, the mechanism of renal secretion of penem antibiotics was examined by using a Xenopus oocyte expression system. Faropenem (an oral penem antibiotic) was transported via Npt1 with a Michaelis-Menten constant of 0.77 ± 0.34 mM in a sodium-independent but chloride ion-sensitive manner. When the concentration of chloride ions was increased, the transport activity of faropenem by Npt1 was decreased. Since the concentration gradient of chloride ions is in the lumen-to-intracellular direction, faropenem is expected to be transported from inside proximal tubular cells to the lumen. So, we tested the release of faropenem from Xenopusoocytes. The rate of efflux of faropenem from Npt1-expressing oocytes was about 9.5 times faster than that from control water-injectedXenopus oocytes. Faropenem transport by Npt1 was significantly inhibited by β-lactam antibiotics such as benzylpenicillin, ampicillin, cephalexin, and cefazolin to 24.9, 40.5, 54.4, and 26.2% of that for the control, respectively. Zwitterionic β-lactam antibiotics showed lesser inhibitory effects on faropenem uptake than anionic derivatives, indicating that Npt1 preferentially transports anionic compounds. Other anionic compounds, such as indomethacin and furosemide, and the anion transport inhibitor 4,4′-diisothiocyanostilbene-2,2′-disulfonic acid significantly inhibited faropenem uptake mediated by Npt1. In conclusion, our results suggest that Npt1 participates in the renal secretion of penem antibiotics.

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