Portable Device for Preparation and Delivery of Gas Mixtures

A simple, portable device for the preparation and delivery of gas mixtures has been designed and constructed. The basic feature of the device is the use of gas flow controllers to maintain stable flow rates over a wide range of downstream pressures, instead of the capillary tubes and water-filled barostats commonly used in gas-mixing devices. Elimination of the barostat avoids problems such as water leakage, the loss of gases through the barostat, and changes in gas pressure due to evaporative loss of water from the barostat. The absence of a barostat also provides a closed system, allowing the use of the device for mixing and delivering of toxic gases. The prototype of the device has been used to prepare mixtures of different gases for more than 1 year and has been found to operate consistently and reproducibly. The actual concentrations of O₂, CO₂, and N₂ in gas mixtures (determined by gas chromatography) immediately after mixing were between 2.2 and 6.6% of the desired values in four performance tests. Fluctuations in concentration of gases in mixtures after 9 days of continuous gas delivery was less than 2% in four performance tests.     

Determination of Natural In Vivo Noble-Gas Concentrations in Human Blood

Although the naturally occurring atmospheric noble gases He, Ne, Ar, Kr, and Xe possess great potential as tracers for studying gas exchange in living beings, no direct analytical technique exists for simultaneously determining the absolute concentrations of these noble gases in body fluids in vivo. In this study, using human blood as an example, the absolute concentrations of all stable atmospheric noble gases were measured simultaneously by combining and adapting two analytical methods recently developed for geochemical research purposes. The partition coefficients determined between blood and air, and between blood plasma and red blood cells, agree with values from the literature. While the noble-gas concentrations in the plasma agree rather well with the expected solubility equilibrium concentrations for air-saturated water, the red blood cells are characterized by a distinct supersaturation pattern, in which the gas excess increases in proportion to the atomic mass of the noble-gas species, indicating adsorption on to the red blood cells. This study shows that the absolute concentrations of noble gases in body fluids can be easily measured using geochemical techniques that rely only on standard materials and equipment, and for which the underlying concepts are already well established in the field of noble-gas geochemistry.     

A low cost gas mixer

A low cost gas mixer for permanent gases and volatile agents is described. The apparatus uses the simple principle that if known volumes of gases are mixed at the same pressure and temperature, then a mixture of known composition results. The apparatus is shown to have an accuracy of better than ± 0.08% vol/vol for gases and volatile agents in two and three part mixtures. For permanent gases the mixer could be used accurately over the concentration range 1–99% vol/vol. For volatile agents the mixer was suitable for mixing concentrations in the low percentage ranges (< 5% vol/vol). Gas mixtures, including volatile agents, could be stored in the mixer for approximately 2 h without changes in concentration outside this limit of accuracy.     

Kinetics of organic compound removal from waste gases with a biological filter

In order to eliminate organic pollutants in waste gases, a biological filter bed technique has been developed, with a high self-regenerating capacity and a low pressure drop. The bed consists of an appropriate filling material (mainly peat compost), in order to let the microorganisms grow on the solid surface and to supply them with inorganic nutrients. Most organic compounds are oxidized to carbon dioxide and water. The compositions of the solid phase and the viable organisms present are such that aging is prevented, as a result of which a relatively high activity can be maintained during a long period of time (years). Experiments have been carried out in laboratory-scale columns with composite gas mixtures at varied concentrations and superficial gas velocities. The (macro) kinetics of the elimination processes have been studied, which enables the prediction of the elimination capacity of the filter bed.     

Decompression outcome following saturation dives with multiple inert gases in rats

This investigation examined the question of whether gas mixtures containing multiple inert gases provide a decompression advantage over mixtures containing a single inert gas. Unanesthetized male albino rats, Rattus norvegicus, were subjected to 2-h simulated dives at depths ranging from 145 to 220 fsw. At pressure, the rats breathed various He-N2-Ar-O2 mixtures (79.1% inert gas-20.9% O2); they were then decompressed rapidly (within 10 s) to surface pressures. The probability of decompression sickness (DCS), measured either as severe bends symptoms or death, was related to the experimental variables in a Hill equation model incorporating parameters that account for differences in the potencies of the three gases and the weight of the animal. The relative potencies of the three gases, which affect the total dose of decompression stress, were determined as significantly different in the following ascending order of potency: He less than N2 less than Ar; some of these differences were small in magnitude. With mixtures, the degree of decompression stress diminished as either N2 or Ar was replaced by He. No obvious advantage or disadvantage of mixtures over the least potent pure inert gas (He) was evident, although limits to the expectation of possible advantage or disadvantage of mixtures were defined. Also, model analysis did not support the hypothesis that the outcome of decompression with multiple inert gases in rats under these experimental conditions can be explained totally by the volume of gas accumulated in the body during a dive.     

Quantitation of dissolved gas content in emulsions and in blood using mass spectrometric detection

Quantitation of dissolved gases in blood or in other biological media is essential for understanding the dynamics of metabolic processes. Current detection techniques, while enabling rapid and convenient assessment of dissolved gases, provide only direct information on the partial pressure of gases dissolved in the aqueous fraction of the fluid. The more relevant quantity known as gas content, which refers to the total amount of the gas in all fractions of the sample, can be inferred from those partial pressures, but only indirectly through mathematical modeling. Here we describe a simple mass spectrometric technique for rapid and direct quantitation of gas content for a wide range of gases. The technique is based on a mass spectrometer detector that continuously monitors gases that are rapidly extracted from samples injected into a purge vessel. The accuracy and sample processing speed of the system is demonstrated with experiments that reproduce within minutes literature values for the solubility of various gases in water. The capability of the technique is further demonstrated through accurate determination of O(2) content in a lipid emulsion and in whole blood, using as little as 20 μL of sample. The approach to gas content quantitation described here should greatly expand the range of animals and conditions that may be used in studies of metabolic gas exchange, and facilitate the development of artificial oxygen carriers and resuscitation fluids.     

Ventilation-perfusion inhomogeneity increases gas uptake: theoretical modeling of gas exchange.

Ventilation-perfusion (VA/Q) inhomogeneity was modeled to measure its effect on gas exchange in the presence of inspired mixtures of two soluble gases using a two-compartment computer model. Theoretical studies involving a mixture of hypothetical gases with equal solubility in blood showed that the effect of increasing inhomogeneity of distributions of either ventilation or blood flow is to paradoxically increase uptake of the gas with the lowest overall uptake in relation to its inspired concentration. This phenomenon is explained by the concentrating effects that uptake of soluble gases exert on each other in low VA/Q compartments. Repeating this analysis for inspired mixtures of 30% O(2) and 70% nitrous oxide (N(2)O) confirmed that, during "steady-state" N(2)O anesthesia, uptake of N(2)O is predicted to paradoxically increase in the presence of worsening VA/Q inhomogeneity.     

The Secretion of Oxygen into the Swim-bladder of Fish : II. The simultaneous transport of carbon monoxide and oxygen

Toadfish, Opsanus tau, L., were maintained in sea water equilibrated with gas mixtures containing a fixed proportion of oxygen and varying proportions of carbon monoxide. The swim-bladder was emptied by puncture, and, after an interval of 24 or 48 hours, the newly secreted gases were withdrawn and analyzed. Both carbon monoxide and oxygen are accumulated in the swim-bladder at tensions greater than ambient. The ratio of concentrations, carbon monoxide (secreted): carbon monoxide (administered) bears a constant relation to the ratio, oxygen (secreted): oxygen (administered). The value of the partition coefficient describing this relation is (α = 5.44). The two gases are considered to compete for a common intracellular carrier mediating their active transport. The suggestion is advanced that the intracellular oxygen carrier is a hemoglobin. Comparison of the proportions of carboxy- and oxyhemoglobin in the blood with the composition of the secreted gas proves that the secreted gases are not evolved directly from combination with blood hemoglobin. The suggestion is advanced that cellular oxygen secretion occurs in the rete mirabile: the rete may build up large oxygen tensions in the gas gland capillaries. It is suggested that the gas gland acts as a valve impeding back diffusion of gases from the swim-bladder.     

Common reeds (Phragmites australis) as sustainable energy source: experimental and modelling analysis of torrefaction and pyrolysis processes

The aim of this study is to apply advanced analytical techniques and kinetic modelling to common reeds (Phragmites australis) to characterize its pyrolysis and torrefaction as possible environmental friendly and sustainable pathways of fuel upgrading. Simultaneous thermogravimetric and differential scanning calorimetry analysis have been carried out on common reeds. The evolved gases during the decomposition process have been analysed by a coupled infrared gas analyser and gas chromatograph/mass spectrometer. Different reed origins (China and Italy) and plant parts (stem and leaves) have been compared. The results have been used to calibrate a torrefaction kinetic model. The model has also been tested simulating a reed torrefaction run occurring in a bench‐scale apparatus, supplementing the chemical analysis with a thermal simulation of the reactor carried out through a finite elements approach. The results show that the proposed modelling approach allows the prediction of the reaction products with a satisfying degree of accuracy. Besides its phytodepuration potential, P. australis has proven to be an interesting natural biomass resource for thermochemical conversion processes and energy production both for its suitability and availability.     

Modern Tumor Marker Discovery in Urology: Surface Enhanced Laser Desorption and Ionization (SELDI)

During the last two decades, biomarker research has benefited from the introduction of new proteomic analytical techniques. In this article, we review the application of surface enhanced laser desorption/ionization time-of-flight (SELDI-TOF) mass spectroscopy in urologic cancer research. After reviewing the literature from MEDLINE on proteomics and urologic oncology, we found that SELDI-TOF is an emerging proteomic technology in biomarker discovery that allows for rapid and sensitive analysis of complex protein mixtures. SELDI-TOF is a novel proteomic technology that has the potential to contribute further to the understanding and clinical exploitation of new, clinically relevant biomarkers.     

Suitability of capacitive sensors for measuring relative humidity in anesthetic gas systems]

A capacitive sensor was tested for its suitability for measuring relative humidity in an anaesthetic gas circuit. The valvo sensor PH1 was tested using various different anaesthetic gas mixtures. Measuring accuracy was influenced neither by such volatile anaesthetics as isoflurane and halothane, nor by oxygen or nitrous oxide. The response time of the sensor depends on its position within the gas, and in the most favourable case is about 3 minutes. The sensor is readily incorporated within an existing gas circuit. The linearity of the characteristic curve must be corrected by external electronic compensation to avoid measuring problems in the lower humidity range.     

Determination of the distribution of ventilation-perfusion ratios: technic of elimination of multiple inert gases

The multiple inert gas elimination technique (MIGT) facilitates the estimation of the distributions of ventilation-perfusion (VA/Q) ratios in the experimental and clinical setting. The most relevant technical aspects and equipment and operational requirements needed to measure a mixture of inert gases in both the gas phase and the blood phase using gas chromatography are overviewed with detail. Results obtained in 3 dogs and 4 syringe-homogeneous lung models were entirely consistent with data formerly reported in the literature. Particular attention is paid to the linearity of the gas chromatograph detectors, reproducibility of inert gases sampling, and analysis of brands of heparin to detect acetone content. The errors of measurement (coefficients of variation) in blood were: 1.4 for sulfur hexafluoride; 1.8% for ethane; 2% for cyclopropane and halothane, each; 2.4% for diethyl ether; and, 3.6% for acetone. Important practical points are also emphasized in order to draw attention to potential problems and issues that should be concentrated upon to minimize the error in the measurements. It is concluded that the setting up of the MIGT is well established and validated.     

Antiapoptotic activity of argon and xenon

Although chemically non-reactive, inert noble gases may influence multiple physiological and pathological processes via hitherto uncharacterized physical effects. Here we report a cell-based detection system for assessing the effects of pre-defined gas mixtures on the induction of apoptotic cell death. In this setting, the conventional atmosphere for cell culture was substituted with gas combinations, including the same amount of oxygen (20%) and carbon dioxide (5%) but 75% helium, neon, argon, krypton, or xenon instead of nitrogen. The replacement of nitrogen with noble gases per se had no effects on the viability of cultured human osteosarcoma cells in vitro. Conversely, argon and xenon (but not helium, neon, and krypton) significantly limited cell loss induced by the broad-spectrum tyrosine kinase inhibitor staurosporine, the DNA-damaging agent mitoxantrone and several mitochondrial toxins. Such cytoprotective effects were coupled to the maintenance of mitochondrial integrity, as demonstrated by means of a mitochondrial transmembrane potential-sensitive dye and by assessing the release of cytochrome c into the cytosol. In line with this notion, argon and xenon inhibited the apoptotic activation of caspase-3, as determined by immunofluorescence microscopy coupled to automated image analysis. The antiapoptotic activity of argon and xenon may explain their clinically relevant cytoprotective effects.     

Microalgal removal of CO<Subscript>2</Subscript> from flue gases: Changes in medium pH and flue gas composition do not appear to affect the photochemical yield of microalgal cultures

Our research objectives are to determine under what conditions microalgal-based CO₂ capture from flue gases is economically attractive. Specifically, our objective here was to select microalgae that are temperature, pH and flue gas tolerant. Microalgae were grown under five different temperatures, three different pH and five different flue gas mixtures besides 100% CO₂ (gas concentrations that the cells were exposed to ranged 5.7–100% CO₂, 0–3504 ppm SO₂, 0–328 ppm NO, and 0–126 ppm NO₂). Our results indicate that the microalgal strains tested exhibit a substantial ability to withstand a wide range of temperature (54 strains tested), pH (20 strains tested) and flue gas composition (24 strains tested) likely to be encountered in cultures used for carbon sequestration from smoke stack gases. Our results indicate that microalgal photosynthesis is a limited but viable strategy for CO₂ capture from flue gases produced by stationary combustion sources.     

A new method for sustained generation of ultra-pure nitric oxide-containing gas mixtures via controlled UVA-photolysis of nitrite solutions

Exogenous gaseous nitric oxide (gNO) is an FDA approved drug for treatment of a variety of human pathologies like Persistent Pulmonary Hypertension in neonates and premature babies, skin lesions and fungal dermatophyte infections. Substantial disadvantages of current gNO-based therapies are the high therapy costs, high storage costs of the gas cylinders, and the rapid contamination of compressed NO gases with various decomposition products. Here we describe a new, very simple, and inexpensive photolytic generator of uncontaminated NO-containing gas mixtures at therapeutic concentrations. The new method bases on UVA-induced and redox-assisted decomposition of nitrite ions in aqueous solutions. NO formation via UVA-induced photolysis of nitrite is accompanied by an OH radical-dependent production of NO₂ that beside its toxic character additionally strongly reduces the NO yield by consuming NO in its reaction to N₂O₃. During the UVA-induced photodecomposition process both, inhibition of NO₂ formation or NO₂ depletion by antioxidants hinders the NO-consuming reaction with NO₂ and ensured a maximal purity and maximal yield of NO-containing gas mixtures. Therefore, NO-containing gas mixtures generated by the described method are suitable for medical applications like inhalation or gassing of chronic non-healing wounds. Control of temperature, UVA intensity and composition of the reaction mixture allows facile control over the final NO level in the carrier gas over a wide concentration range. We demonstrate the sustained and stable release of NO over a wide dynamic range (10–5000 ppm NO) for many hours. The method avoids contamination-prone long time storage of NO gas. As such, it appears particularly relevant for applications involving the additional presence of oxygen (e.g. inhalation).     

Allocation of Process Gases Generated from Integrated Steelworks by an Improved System Expansion Method (7 pp)

Goal, Scope and Background Although a large number of life cycle inventory (LCI) analyses for steel-making processes or steel products have been conducted, the allocation of process gases generated from the steelworks has not yet been clearly solved. The most consistent settlement for avoiding the allocation problem has been generally known as a system expansion method. However, the existing subtracted operations for the process gases in that method are inconsistent to a system in which those gases are consumed at their unbalanced consumption ratio. The goal of this study is to suggest a more reasonable substitute for the process gases in the system expansion method and a modified system expansion method resettling the amount of process gases used. Methods To seek a more suitable one as a substituted operation of the process gas, a kind of by-product gas, in the system expansion method, it is necessary to analyze the composition of whole fuel consumed within a steelworks. Because the steelworks is supplied with a gap of electricity from the national grid electricity other than home power plants, we should also consider various carbon fossil fuels consumed in the external electric-power production. From this procedure, a composite fuel, which is composed of coal, heavy fuel oil and LNG, is derived as the alternative of the process gases such as BFG, COG, CFG, and LDG. In the sequential manufacturing line, IO(gas), which is the ratio of the quantity used to the quantity produced of each process gas, is increased as a functional unit proceeds to a following steel product of the next process. In the LCI system, where IO(gas) is higher than one, the IO(gas) is adjusted to nearly one. The adjustment of IO is conducted in the order of the amount of process gas used in the whole steelworks on the basis of the functional unit. Results and Discussion LCI analyses were carried out focusing on the alternative of the process gases for five steel products. As a functional unit goes down a lower stage, IO(gas) is increased due to the high consumption of those gases. We found a phenomenon that IO(gas) had a critical influence on the LCI results between no allocation and system expansion for the process gases through sensitivity analysis. To reduce this influence and adjust for the real situation of IO(gas), we applied an improved system expansion method to the process gases. That is, we partly substituted a process gas with LNG and rearranged the ratio between internal and external electricity (RIEE) as close as the values of IO(gas) to one. Conclusion As the alternative fuel for the process gases, a composite fuel was derived in the system expansion method. In addition to the composite fuel, which consisted of coal, HFO and LNG, an improved system expansion method was revised by adjusting a modified IO(gas) to nearly one, not the high value of IO(gas) for each process gas. Recommendation and Outlook This improved system expansion method can be applicable in the chemical industry as well as the steel industry, which have multi-function systems. Optimal LCI analysis may be achieved through the redistribution and optimization in the usage of process gases.     

Greenhouse gas emission during storage of pig manure on a pilot scale

The greenhouse gas emissions (CO2, CH4, N2O) from a 2 ton (4.4 m3) deep litter pig manure pile (storage time 113 days during winter season) were quantified by using a tent, which covered the whole pile during the measuring periods only. The emissions were calculated in CO2 equivalents per kilogram dry matter by. Additionally the retention time (use of tracer gas SF6) and the concentrations of the gases in different parts of the pile were determined. The average retention time of the gases in the pile was less than 2 h. CH4 is assumed to have been generated only in the centre of the pile, whereas CO2 was assumed to have been generated in a wider zone. The emissions of CH4, CO2 and N2O were at the highest in the beginning when nearly the whole pile had temperatures in the range of thermophilic microorganisms. This leads to the assumption that mainly thermophilic microorganisms formed the gases. The most important gas for global warming was found to be nitrous oxide.     

Estimating the Toxicity of Pesticide Mixtures to Aquatic Organisms: A Review

A major difficulty in addressing chemical mixtures through legislation or regulations revolves around our limited understanding of their potential impacts. This review provides an overview of recent research on pesticide mixture toxicity to aquatic biota and the methods employed to predict toxic effects. The most common approaches are to assume concentration-addition or independent action of chemicals in a mixture. There are a number of cases in the literature of interactions between pesticides. However, models accounting for possible interactions between mixture components are used infrequently. Although results are limited, studies investigating the effects of pesticide mixtures have not demonstrated significant synergism at environmentally relevant concentrations. Based on the results of our review, we conclude that the concentration-addition model is a generally conservative and practical first-tier model for the ecological assessment of pesticide mixtures in aquatic systems.     

A method for controlling the within-root CO2 concentration

Abstract A method is presented for the control of carbon dioxide concentrations within the roots of Fraxinus pennsylvanica Marsh. The results indicated a linear fit of the root CO₂ concentrations to the CO₂ levels of the treatment gases: y= l.l. x+105 (r= 0.98, 18 d.f.). The method presented for controlling CO₂ can be easily modified for other gas mixtures and plant species.