Sorption and desorption of phosphorus by shale: batch and column studies

2010 ◽  
Vol 61 (3) ◽  
pp. 599-606 ◽  
Author(s):  
Johnsely S. Cyrus ◽  
G. B. Reddy
Keyword(s):  
Residence Time ◽  
Flow Rate ◽  
Nutrient Release ◽  
Phosphorus Sorption ◽  
Column Studies ◽  
Desorption Process ◽  
Low Concentrations ◽  
Sorbent Materials ◽  
High Concentrations ◽  
The Cost

Constructed wetland systems have gained attention as attractive solutions for wastewater treatment. Wetlands are not efficient to treat wastewater with high concentrations of phosphorus (P). In order to remove high soluble P loads by wetland, sorbent beds can be added prior to the discharge of wastewater into wetlands. Sorption by sorbent materials is identified as a method for trapping excess P in wastewaters. In the present investigation, shale has been identified as a sorbent material for removal of phosphate (PO4-P) due to the cost effectiveness, stability and possibility of regeneration. The study focuses on the removal of PO4-P from wastewater using shale and the feasibility of using the P-sorbed material as slow-release fertilizer. Phosphorus sorption experiments were conducted by using shale (2 mm and 2–4.7 mm). Results indicate that Shale I (particle size = 2 mm) showed the highest sorption of PO4-P (500 ± 44 mg kg−1). Breakthrough point was reached within 10 h in columns with flow rates of 2 and 3 ml min−1. Lower flow rate of 1 ml min−1 showed an average residence time of about 2 h while columns with a higher flow rate of 3 ml min−1 showed a residence time of about 40 minutes. Variation in flow rate did not influence the desorption process. Since very low concentrations of PO4-P are released, Shale saturated with PO4-P may be used as a slow nutrient release source of P or as a soil amendment. The sorbent can also be regenerated by removing the sorbed PO4-P by using 0.1 N HCl.

Direct and indirect actions of radiation on viruses and enzymes

Parasitology ◽  
1944 ◽  
Vol 36 (1-2) ◽  
pp. 110-118 ◽  
Author(s):  
Douglas Lea ◽  
Kenneth M. Smith ◽  
Barbara Holmes ◽  
Roy Markham
Keyword(s):  
British Empire ◽  
X Rays ◽  
X Ray ◽  
Low Concentrations ◽  
Biochemical Laboratory ◽  
Γ Rays ◽  
High Concentrations ◽  
Concentrated Solution ◽  
The Cost ◽  
Indirect Action

1. The inactivation by γ-rays of tobacco mosaic virus is studied at various concentrations. It is found that the inactivation dose is independent of concentration at high concentrations, and at low concentrations also attains a constant, but lower, value. Over an intermediate range the inactivation dose increases with increase of concentration.2. These facts are explained on the basis that when irradiated dry or in concentrated solution the inactivation is direct and due to ionization produced inside the virus particle. At lower concentrations the inactivation is largely indirect and due to ionization of the water.3. Gelatin added to the solution protects the virus against the indirect action of radiation.4. Curves are given of the inactivation of dry preparations of ribonuclease and adenylpyro-phosphatase (myosin) by X-rays.5. It is shown that on the assumption that a single ionization in an enzyme molecule leads to its inactivation, measurement of the inactivation dose leads to a rough estimate of the molecular weight of the enzyme.6. There appears to be no fundamental difference in the mechanism of radiation-inactivation of viruses and enzymes.All irradiations were carried out at the Strangeways Laboratory. The virus was prepared and tested at the Plant Virus Station and the Molteno Institute. The enzymes were prepared and estimated at the Biochemical Laboratory. We are indebted to the British Empire Cancer Campaign for defraying the cost of the X-ray equipment at the Strangeways Laboratory.

Neutrophil Elastase Potentiates Cathepsin G-lnduced Platelet Activation

1992 ◽  
Vol 68 (05) ◽  
pp. 570-576 ◽  
Author(s):  
Mary A Selak
Keyword(s):  
Neutrophil Elastase ◽  
Cell Activation ◽  
Thromboxane A2 ◽  
Creatine Phosphate ◽  
Dense Granule ◽  
Cathepsin G ◽  
Dependent Manner ◽  
Concentration Dependent Manner ◽  
Low Concentrations ◽  
High Concentrations

SummaryWe have previously demonstrated that human neutrophil cathepsin G is a strong platelet agonist that binds to a specific receptor. This work describes the effect of neutrophil elastase on cathepsin G-induced platelet responses. While platelets were not activated by high concentrations of neutrophil elastase by itself, elastase enhanced aggregation, secretion and calcium mobilization induced by low concentrations of cathepsin G. Platelet aggregation and secretion were potentiated in a concentration-dependent manner by neutrophil elastase with maximal responses observable at 200 nM. Enhancement was observed when elastase was preincubated with platelets for time intervals of 10–60 s prior to addition of a low concentration of cathepsin G and required catalytically-active elastase since phenylmethanesulphonyl fluoride-inhibited enzyme failed to potentiate cell activation. Neutrophil elastase potentiation of platelet responses induced by low concentrations of cathepsin G was markedly inhibited by creatine phosphate/creatine phosphokinase and/or indomethacin, indicating that the synergism between elastase and cathepsin G required the participation of ADP and thromboxane A2. On the other hand, platelet responses were not attenuated by the PAF antagonist BN 52021, signifying that PAF-acether did not play a role in elastase potentiation. At higher concentrations porcine pancreatic elastase exhibits similar effects to neutrophil elastase, demonstrating that the effect of elastase was not unique to the neutrophil protease. While neutrophil elastase failed to alter the ability of cathepsin G to hydrolyze a synthetic chromogenic substrate, preincubation of platelets with elastase increased the apparent affinity of cathepsin G binding to platelets. In contrast to their effect on cathepsin G-induced platelet responses, neither neutrophil nor pancreatic elasatse potentiated aggregation or dense granule release initiated by ADP, PAF-acether, arachidonic acid or U46619, a thromboxane A2 mimetic. Moreover, unlike its effect on cathepsin G, neutrophil elastase inhibited thrombin-induced responses. The current observations demonstrate that elastase can potentiate platelet responses mediated by low concentrations of cathepsin G, suggesting that both enzymes may function synergistically to activate platelets under conditions where neutrophil degranulation occurs.

In Vitro Effects of Ethanol on Rabbit Platelet Aggregation, Secretion of Granule Contents, and Cyclic AMP Levels in the Presence of Prostacyclin

1989 ◽  
Vol 61 (02) ◽  
pp. 254-258 ◽  
Author(s):  
Margaret L Rand ◽  
Peter L Gross ◽  
Donna M Jakowec ◽  
Marian A Packham ◽  
J Fraser Mustard
Keyword(s):  
Cyclic Amp ◽  
Inhibitory Effect ◽  
Rabbit Platelet ◽  
Inhibitory Effects ◽  
Low Concentrations ◽  
Rabbit Platelets ◽  
High Concentrations ◽  
In Vitro Effects ◽  
Aggregation Of Platelets

SummaryEthanol, at physiologically tolerable concentrations, inhibits platelet responses to low concentrations of collagen or thrombin, but does not inhibit responses of washed rabbit platelets stimulated with high concentrations of ADP, collagen, or thrombin. However, when platelet responses to high concentrations of collagen or thrombin had been partially inhibited by prostacyclin (PGI2), ethanol had additional inhibitory effects on aggregation and secretion. These effects were also observed with aspirin- treated platelets stimulated with thrombin. Ethanol had no further inhibitory effect on aggregation of platelets stimulated with ADP, or the combination of ADP and epinephrine. Thus, the inhibitory effects of ethanol on platelet responses in the presence of PGI2 were very similar to its inhibitory effects in the absence of PGI2, when platelets were stimulated with lower concentrations of collagen or thrombin. Ethanol did not appear to exert its inhibitory effects by increasing cyclic AMP above basal levels and the additional inhibitory effects of ethanol in the presence of PGI2 did not appear to be brought about by further increases in platelet cyclic AMP levels.

Aggregation of Cat Platelets in Vitro

1970 ◽  
Vol 23 (03) ◽  
pp. 601-620 ◽  
Author(s):  
Th. B Tschopp
Keyword(s):  
Adenosine Monophosphate ◽  
Blood Collection ◽  
Base Line ◽  
Reversible Aggregation ◽  
Low Concentrations ◽  
Irreversible Aggregation ◽  
High Concentrations ◽  
Two Phases ◽  
Improved Technique

SummaryAggregation of cat platelets in the citrated plasma is examined by means of Born’s absorptiometer. A marked tendency of the platelets of this species to spontaneous aggregation necessitated first of all the development of an improved technique of blood collection.A hypothesis according to which 5-HT is released from the platelets, explains the absence of oscillations on the base line of the absorptiometer, the absence of platelet swelling, when ADP is added, and the effect of stirring on the aggregation curves in cat PRP. The average volume of cat platelets amounts to 10.46 μ3 when directly fixed in the blood, when fixed from PRP to 12.17 μ3, when fixed from stirred PRP to 13.51 μ3.In low concentrations (0.3-2 μM) ADP produce reversible aggregation; in narrowly restricted, individually dissimilar mean concentrations irreversible aggregation in two phases and in high concentrations, irreversible aggregation in one phase. Like ADP serotonin produces 2 phase irreversible aggregation in concentrations of 3-10 μM, but unlike ADP, the aggregation velocity decreases again with high 5-HT concentrations (>100 μM). Adrenaline does not produce aggregation and it is likely that adenosine and adenosine monophosphate inhibit the aggregation by serotonin but not by ADP. Species differences in the aggregation of human, rabbit and cat platelets are discussed.

The Action of an Aniline Derivative (AN 162) on Blood Coagulation and on Platelets

1971 ◽  
Vol 26 (01) ◽  
pp. 145-166
Author(s):  
E Deutsch ◽  
K Lechner ◽  
K Moser ◽  
L Stockinger
Keyword(s):  
Blood Coagulation ◽  
Citric Acid Cycle ◽  
Second Phase ◽  
Aniline Derivative ◽  
Acid Cycle ◽  
Enhancing Effect ◽  
Low Concentrations ◽  
Dual Action ◽  
High Concentrations ◽  
Induced Aggregation

Summary1. The aniline derivative AN 162, Donau Pharmazie, Linz, Austria, has a dual action on the blood coagulation: an anticoagulant and an coagulation enhancing effect.2. The anticoagulant action may only be demonstrated with high concentrations (over 1 X 10”3 M related to plasma) preferentially in PPP. It is partially caused by an inhibition of the endogenous way of generation of the prothrombin converting principle. In addition it is suggested that it interferes with the fibrinogen-fibrin reaction in a manner not yet understood.3. The coagulant action is caused by a greater availability of platelet constituents at low concentrations of AN 162 (over 1 × 10-4 M) and by the induction of a release reaction at higher concentrations. The platelet factors 3 and 4, serotonin, adenine, and acid phosphatase are released.4. AN 162 inhibits platelet aggregation. This inhibition can be demonstrated by the PAT of Breddin and in the stirred aggregation test of Born. It is more effective to inhibit the collagen-induced and the second phase of the adrenaline-induced aggregation than the ADP induced one. The platelet retention (test of Hellem) is also reduced.5. The action of AN 162 on the platelets is caused by a damage of the platelet membrane which becomes permeabel for both, soluble platelet constitutents and granula.6. AN 162 interferes with the energy metabolism of the platelets. It causes a loss of ATP, and inhibits the key-enzymes of glycolysis, citric acid cycle, fatty acid oxydation and glutathione reduction.7. AN 162 inhibits the growth of fibroblasts without influence on mitosis.

Functional Involvement of Thrombospondin in Platelet Aggregation Induced by Low Versus High Concentrations of Thrombin

1986 ◽  
Vol 55 (01) ◽  
pp. 136-142 ◽  
Author(s):  
K J Kao ◽  
David M Shaut ◽  
Paul A Klein
Keyword(s):  
Platelet Aggregation ◽  
Binding Sites ◽  
Inhibitory Effect ◽  
Activated Platelets ◽  
Low Concentrations ◽  
Platelet Binding ◽  
Functional Involvement ◽  
Thrombin Activation ◽  
Platelet Aggregates ◽  
High Concentrations

SummaryThrombospondin (TSP) is a major platelet secretory glycoprotein. Earlier studies of various investigators demonstrated that TSP is the endogenous platelet lectin and is responsible for the hemagglutinating activity expressed on formaldehyde-fixed thrombin-treated platelets. The direct effect of highly purified TSP on thrombin-induced platelet aggregation was studied. It was observed that aggregation of gel-filtered platelets induced by low concentrations of thrombin (≤0.05 U/ml) was progressively inhibited by increasing concentrations of exogenous TSP (≥60 μg/ml). However, inhibition of platelet aggregation by TSP was not observed when higher than 0.1 U/ml thrombin was used to activate platelets. To exclude the possibility that TSP inhibits platelet aggregation by affecting thrombin activation of platelets, three different approaches were utilized. First, by using a chromogenic substrate assay it was shown that TSP does not inhibit the proteolytic activity of thrombin. Second, thromboxane B2 synthesis by thrombin-stimulated platelets was not affected by exogenous TSP. Finally, electron microscopy of thrombin-induced platelet aggregates showed that platelets were activated by thrombin regardless of the presence or absence of exogenous TSP. The results indicate that high concentrations of exogenous TSP (≥60 μg/ml) directly interfere with interplatelet recognition among thrombin-activated platelets. This inhibitory effect of TSP can be neutralized by anti-TSP Fab. In addition, anti-TSP Fab directly inhibits platelet aggregation induced by a low (0.02 U/ml) but not by a high (0.1 U/ml) concentration of thrombin. In conclusion, our findings demonstrate that TSP is functionally important for platelet aggregation induced by low (≤0.05 U/ml) but not high (≥0.1 U/ml) concentrations of thrombin. High concentrations of exogenous TSP may univalently saturate all its platelet binding sites consequently interfering with TSP-crosslinking of thrombin-activated platelets.

ABOLITION OF MAGNESIUM-INDUCED HYPOCALCAEMIA BY ACUTE THYRO-PARATHYROIDECTOMY IN THE CAT

1970 ◽  
Vol 64 (1) ◽  
pp. 150-158 ◽  
Author(s):  
S. Pors Nielsen
Keyword(s):  
Sodium Chloride ◽  
Flow Rate ◽  
Magnesium Chloride ◽  
Calcium Concentration ◽  
Plasma Calcium ◽  
Magnesium Concentration ◽  
Isotonic Sodium Chloride ◽  
Plasma Calcium Concentration ◽  
High Concentrations ◽  
Plasma Magnesium

ABSTRACT Intravenous infusion of isotonic magnesium chloride into young cats with a resultant mean plasma magnesium concentration of 7.7 meq./100 g protein was followed by a significant lowering of the plasma calcium concentration in 90 minutes. The rate of decrease of plasma calcium is consistent with the hypothesis that calcitonin is released by magnesium in high concentrations. There was no decrease in the plasma calcium concentration in cats of the same weight thyroparathyroidectomized 60 min before an identical magnesium chloride infusion or an infusion of isotonic sodium chloride at the same flow rate. The hypercalciuric effect of magnesium could not account for the hypocalcaemic effect of magnesium. Plasma magnesium concentration during magnesium infusion into cats with an intact thyroid-parathyroid gland complex was slightly, but not significantly higher than in acutely thyroparathyroidectomized cats.

BIO-FUEL PRODUCTION FROM CARBONDIOXIDE GAS USING S. elongatus PCC 7942 FROM CYANOBACTERIA

2020 ◽  
Vol 2 (1) ◽  
Author(s):  
Delia Teresa Sponza ◽  
Cansu Doğanx
Keyword(s):  
Flow Rate ◽  
Maximum Yield ◽  
Butanol Production ◽  
Fuel Production ◽  
Cost Analyses ◽  
Operational Conditions ◽  
O2 Concentration ◽  
The Cost ◽  
Pcc 7942 ◽  
Dissolved O2

The scope of this study, is  1-butanol production from CO2 with S. elongatus PCC 7942 culture. The yields of 1-butanolproduced/CO2utilized have been calculated. The maximum concentration of produced 1- butanol is 35.37 mg/L and 1-butanolproduced/CO2utilized efficiency is 92.4. The optimum operational conditions were  30°C temperature, 60 W intensity of light, pH= 7.1, 120 mV redox potential, 0.083 m3/sn flow rate with CO2 and 0.5 mg/l dissolved O2 concentration. Among the enzymes on the metabolic trail of the production of 1-butanol via using S. elongatus PCC 7942 cyanobacteria. At maximum yield; the measured concentrations are 0.016 µg/ml for hbd; 0.0022 µg/ml for Ter and 0.0048 µg/ml for AdhE2. The cost analyses necessary for 1-butanol production has been done and the cost of 1 litre 1-butanol has been determined as maximum 1.31 TL/L.

Removal of trichloroethylene and trichloroethane using a novel hollow-fibre gas-permeable membrane

2003 ◽  
Vol 3 (5-6) ◽  
pp. 67-72
Author(s):  
S. Takizawa ◽  
T. Win
Keyword(s):  
Boundary Layer ◽  
Flow Regime ◽  
Removal Efficiency ◽  
Residence Time ◽  
Flow Rate ◽  
Air Flow ◽  
Hollow Fibre ◽  
Permeation Rate ◽  
Permeable Membrane ◽  
Diffusional Boundary Layer

In order to evaluate effects of operational parameters on the removal efficiency of trichloroethylene and 1,1,1-trichloroethene from water, lab-scale experiments were conducted using a novel hollow-fibre gaspermeable membrane system, which has a very thin gas-permeable membrane held between microporous support membranes. The permeation rate of chlorinated hydrocarbons increased at higher temperature and water flow rate. On the other hand, the effects of the operational conditions in the permeate side were complex. When the permeate side was kept at low pressure without sweeping air (pervaporation), the removal efficiency of chlorinated hydrocarbon, as well as water permeation rate, was low probably due to lower level of membrane swelling on the permeate side. But when a very small amount of air was swept on the membrane (air perstripping) under a low pressure, it showed a higher efficiency than in any other conditions. Three factors affecting the permeation rate are: 1) reduction of diffusional boundary layer within the microporous support membrane, 2) air/vapour flow regime and short cutting, and 3) the extent of membrane swelling on the permeate side. A higher air flow, in general, reduces the diffusional boundary layer, but at the same time disrupts the flow regime, causes short cutting, and makes the membrane dryer. Due to these multiple effects on gas permeation, there is an optimum operational condition concerning the vacuum pressure and the air flow rate. Under the optimum operational condition, the residence time within the hollow-fibre membrane to achieve 99% removal of TCE was 5.25 minutes. The log (removal rate) was linearly correlated with the average hydraulic residence time within the membrane, and 1 mg/L of TCE can be reduced to 1 μg/L (99.9% removal).

Biological Mechanisms of H2S Formation in Sewer Pipes

1992 ◽  
Vol 26 (3-4) ◽  
pp. 907-914 ◽  
Author(s):  
A. Attal ◽  
M. Brigodiot ◽  
P. Camacho ◽  
J. Manem
Keyword(s):  
Suspended Solid ◽  
Urban Wastewater ◽  
Biological Mechanisms ◽  
Sewer Pipes ◽  
Sulfate Reducing ◽  
Biological Phenomena ◽  
Low Concentrations ◽  
Production Of Hydrogen ◽  
High Concentrations ◽  
Reducing Bacteria

The purpose of this study is to gain a better understanding of the biological phenomena involved in the production of hydrogen sulfide in urban wastewater (UWW) systems. It is found that the UWW itself naturally possesses the biomass needed to consume the sulfates. These heterotrophic sulfate-reducing bacteria populations, though immediately active in strict anaerobic conditions, are present only in very low concentrations in the UWW. A concentration of them was studied within the pressure pipes, in the form of deposits, and this justifies the high concentrations of sulfides measured in certain wastewater networks. There are two reasons why the ferrous sulfate used as a treatment in any wastewater networks should not cause the production of additional sulfides. Firstly, the sulfate consumption kinetics are always too slow, relative to the residence time of the water in the pipe, for all of the sulfates to be consumed anyway. Secondly, the amount of assimilable carbon, soluble carbon, and carbon from suspended solid (SS) hydrolysis is insufficient.

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