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At least 145 records · Page 8

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DOE OSTI2013

Analysis Of 2h-Evaporator Scale Wall [HTF-13-82] And Pot Bottom [HTF-13-77] Samples

Savannah River Remediation (SRR) is planning to remove a buildup of sodium aluminosilicate scale from the 2H-evaporator pot by loading and soaking the pot with heated 1.5 M nitric acid solution. Sampling and analysis of the scale material has been performed so that uranium and plutonium isotopic analysis can be input into a Nuclear Criticality Safety Assessment (NCSA) for scale removal by chemical cleaning. Historically, since the operation of the Defense Waste Processing Facility (DWPF), silicon in the DWPF recycle stream combines with aluminum in the typical tank farm supernate to form sodium aluminosilicate scale mineral deposits in the 2Hevaporator pot and gravity drain line. The 2H-evaporator scale samples analyzed by Savannah River National Laboratory (SRNL) came from the bottom cone sections of the 2H-evaporator pot [Sample HTF-13-77] and the wall 2H-evaporator [sample HTF-13-82]. X-ray diffraction analysis (XRD) confirmed that both the 2H-evaporator pot scale and the wall samples consist of nitrated cancrinite (a crystalline sodium aluminosilicate solid) and clarkeite (a uranium oxy-hydroxide mineral). On “as received” basis, the bottom pot section scale sample contained an average of 2.59E+00 ± 1.40E-01 wt % total uranium with a U-235 enrichment of 6.12E-01 ± 1.48E-02 %, while the wall sample contained an average of 4.03E+00 ± 9.79E-01 wt % total uranium with a U-235 enrichment of 6.03E-01% ± 1.66E-02 wt %. The bottom pot section scale sample analyses results for Pu-238, Pu-239, and Pu-241 are 3.16E- 05 ± 5.40E-06 wt %, 3.28E-04 ± 1.45E-05 wt %, and <8.80E-07 wt %, respectively. The evaporator wall scale samples analysis values for Pu-238, Pu-239, and Pu-241 averages 3.74E-05 ± 6.01E-06 wt %, 4.38E-04 ± 5.08E-05 wt %, and <1.38E-06 wt %, respectively. The Pu-241 analyses results, as presented, are upper limit values. These results are provided so that SRR can calculate the equivalent uranium-235 concentrations for the NCSA. Results confirm that the uranium contained in the scale remains depleted with respect to natural uranium. SRNL did not calculate an equivalent U-235 enrichment, which takes into account other fissionable isotopes U-233, Pu-239 and Pu-241. The applicable method for calculation of equivalent U-235 will be determined in the NCSA.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

DOE OSTI2017

Preparation and evaporation of Hanford Waste treatment plant direct feed low activity waste effluent management facility simulant

The Hanford Waste Treatment and Immobilization Plant (WTP) Low Activity Waste (LAW) vitrification facility will generate an aqueous condensate recycle stream (LAW Melter Off-Gas Condensate, LMOGC) from the off-gas system. The baseline plan for disposition of this stream during full WTP operations is to send it to the WTP Pretreatment Facility, where it will be blended with LAW, concentrated by evaporation, and recycled to the LAW vitrification facility. However, during the Direct Feed LAW (DFLAW) scenario, planned disposition of this stream involves concentrating the condensate in a new evaporator at the Effluent Management Facility (EMF) and returning it to the LAW melter. The LMOGC stream will contain components, e.g. halides and sulfates, that are volatile at melter temperatures, have limited solubility in glass waste forms, and present a material corrosion concern. Because this stream will recycle within WTP, these components are expected to accumulate in the LMOGC stream, exacerbating their impact on the number of LAW glass containers that must be produced. Diverting the stream reduces the halides and sulfates in the glass and is a key objective of this program. In order to determine the disposition path, it is key to experimentally determine the fate of contaminants. To do this, testing is needed to account for the buffering chemistry of the components, determine the achievable evaporation end point, identify insoluble solids that form, determine the formation and distribution of key regulatoryimpacting constituents, and generate an aqueous stream that can be used in testing of the subsequent immobilization step. This overall program examines the potential treatment and immobilization of the LMOGC stream to enable alternative disposal. The objective of this task was to (1) prepare a simulant of the LAW Melter Off-gas Condensate expected during DFLAW operations, (2) demonstrate evaporation in order to predict the final composition of the effluents from the EMF evaporator to aid in planning for their disposition, and (3) generate concentrated evaporator bottoms for use in immobilization testing.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

DOE OSTI2023

Laser heating and evaporation of a single droplet

The laser technology is being abundantly studied for controlled energy deposition for a range of applications in aerodynamic flow control, material processing, ignition, and combustion. The absorption of laser radiation by liquid droplets affects further propagation of laser in the atmosphere and causes bleaching of suspended droplets while the ignition and combustion characteristics in combustors are influenced by the evaporation rate of the sprayed fuel. In this work, we present a multi-dimensional mathematical model built on OpenFOAM for laser heating and evaporation of a single droplet in the diffusion dominated regime taking into account absorption of the laser radiation, evaporation process and vapor flow dynamics. The developed solver is validated against available experimental and numerical data for the ethanol and water droplet heating and evaporation. For continuous heating the peak temperature is established by the balance of cooling, evaporation and heating and results in high temperature for larger droplets. It has been shown that for heating by a single laser pulse the maximum temperature of droplets depends only on the peak intensity of the laser radiation. Furthermore, for the peak irradiance close to the transition to the boiling regime, temporal dynamics of the droplet temperature is independent of the droplet size. With proper normalization of time, the dynamics of the droplet shrinkage and cooling is shown to be independent of droplet sizes and peak laser intensities. The influence of cooling and evaporation processes on droplet heating was found to be controlled by the pulse repetition rate for repeated pulse operation.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗

DOE OSTI2017

The influence of land cover on surface energy partitioning and evaporative fraction regimes in the U.S. Southern Great Plains

Land-atmosphere interactions are important to climate prediction, but the underlying effects of surface forcing of the atmosphere are not well understood. In the U.S. Southern Great Plains, grassland/pasture and winter wheat are the dominant land covers but have distinct growing periods that may differently influence land-atmosphere coupling during spring and summer. Variables that influence surface flux partitioning can change seasonally, depending on the state of local vegetation. We use surface observations from multiple sites in the U.S. Department of Energy Atmospheric Radiation Measurement Southern Great Plains Climate Research Facility and statistical modeling at a paired grassland/agricultural site within this facility to quantify land cover influence on surface energy balance and variables controlling evaporative fraction (latent heat flux normalized by the sum of sensible and latent heat fluxes). We demonstrate that the radiative balance and evaporative fraction are closely related to green leaf area at both winter wheat and grassland/pasture sites and that the early summer harvest of winter wheat abruptly shifts the relationship between evaporative fraction and surface state variables. Prior to harvest, evaporative fraction of winter wheat is strongly influenced by leaf area and soil-atmosphere temperature differences. After harvest, variations in soil moisture have a stronger effect on evaporative fraction. Finally, this is in contrast with grassland/pasture sites, where variation in green leaf area has a large influence on evaporative fraction throughout spring and summer, and changes in soil-atmosphere temperature difference and soil moisture are of relatively minor importance.

54 ENVIRONMENTAL SCIENCES↗

DOE OSTI2017

Global variation of transpiration and soil evaporation and the role of their major climate drivers

Although global variation in actual evapotranspiration has been widely investigated, it remains unclear how its two major components, transpiration and soil evaporation, are driven by climate drivers across global land surface. This paper uses a well-validated, process-based model that estimates transpiration and soil evaporation, and for the first time investigates and quantifies how the main global drivers, associated to vegetation process and the water and energy cycle, drive the spatiotemporal variation of the two components. The results show that transpiration and soil evaporation dominate the variance of actual evapotranspiration in wet and dry regions, respectively. Dry southern hemisphere from 13°S to 27°S is highlighted since it contributes to 21% global soil evaporation variance, with only 11% global land area. In wet regions, particularly in the humid tropics, there are strong correlations between transpiration, actual evapotranspiration, and potential evapotranspiration, with precipitation playing a relatively minor role, and available radiative energy is the major contributor to the interannual variability in transpiration and actual evapotranspiration in Amazonia. Conversely in dry regions, there are strong correlations between soil evaporation, actual evapotranspiration, and precipitation. Lastly, our findings highlight that ecohydrological links are highly related to climate regimes, and the small region such as Australia has important contribution to interannual variation in global soil evaporation and evapotranspiration, and anthropogenic activities strongly influence the variances in irrigation regions

54 ENVIRONMENTAL SCIENCES↗

DOE OSTI2017

Elimination of inter-discharge helium glow discharge cleaning with lithium evaporation in NSTX

Operation in the National Spherical Torus Experiment (NSTX) typically used either periodic boronization and inter-shot helium glow discharge cleaning (HeGDC), or inter-shot lithium evaporation without boronization, and initially with inter-shot HeGDC. To assess the viability of operation without HeGDC, dedicated experiments were conducted in which Li evaporation was used while systematically shrinking the HeGDC between shots from the standard 10 min to zero (10 → 6.5 → 4 → 0). Good shot reproducibility without HeGDC was achieved with lithium evaporations of 100 mg or higher; evaporations of 200–300 mg typically resulted in very low ELM frequency or ELM-free operation, reduced wall fueling, and improved energy confinement. The use of HeGDC before lithium evaporation modestly reduced D α in the outer scrape-off layer, but not at the strike point. Pedestal electron and ion temperature also improved modestly, suggesting that HeGDC prior to lithium evaporation is a useful tool for experiments that seek to maximize plasma performance.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗

DOE OSTI2015

Nanoscale Measurement of Laser-Induced Temperature Rise and Field Evaporation Effects in CdTe and GaN

The measurement of laser-induced temperature change and its influence on the field evaporation behavior in nanoscale CdTe and GaN specimens was assessed through systematic studies using laser pulsed atom probe tomography. For CdTe, the laser was shown to induce a linear thermal response in the material. Using the determined relationships, a phase map of the field evaporation behavior was created. This shows that at high base temperatures, high laser energies, or low fields, significant Cd sublimation occurs, leading to apparently Te-rich measured compositions. In contrast, the highest fields result in simultaneous evaporation of multiple Te species, leading to apparently Cd-rich measured compositions. For GaN, increasing laser energy reduced the applied bias necessary for a given detection rate, whereas base temperature changes produced no significant effect on the evaporation behavior, indicative of a largely athermal evaporation mechanism. Similarly, the laser energy and bias affected the measured compositions, whereas the base temperature did not. Additionally, the field evaporation behavior in GaN appears unusual in that there is a strong crystallographic dependence resulting in a nonuniform field being maintained across the apex of the specimen. Furthermore, these methods are useful beyond atom probe analyses for elucidating information about bonding and optoelectronic properties

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

DOE OSTI2017

Surprising Effects of Hydrochloric Acid on the Water Evaporation Coefficient Observed by Raman Thermometry

© 2017 American Chemical Society. The kinetics and energetics of cloud droplet and aerosol formation in the atmosphere are strongly influenced by the evaporation and condensation rates of water, yet the magnitude and mechanism of evaporation remains incompletely characterized. Of particular import (and controversy) is the nature of interfacial water pH and its potential effects on evaporation rate and environmental reactivity. We have used Raman thermometry measurements of freely evaporating microdroplets to determine evaporation coefficients (Î) for two different hydrochloric acid solutions, both of which result in a significant deviation from Îwater. At 95% confidence, we find the evaporation coefficient for 1.0 M HCl to be 0.24 ± 0.04, a â-60% decrease relative to pure water, and for 0.1 M HCl to be 0.91 ± 0.08, a â-45% increase relative to pure water. These results suggest a large perturbation in the surface structure induced by either hydronium ions adsorbing to the water surface or by the presence of a Cl-···H3O+ ion-pair moiety in the interfacial region.

Rizzuto, Anthony M↗

DOE OSTI2015

Scaling up nanoscale water-driven energy conversion into evaporation-driven engines and generators

Evaporation is a ubiquitous phenomenon in the natural environment and a dominant form of energy transfer in the Earth’s climate. Engineered systems rarely, if ever, use evaporation as a source of energy, despite myriad examples of such adaptations in the biological world. In this work, we report evaporation-driven engines that can power common tasks like locomotion and electricity generation. These engines start and run autonomously when placed at air–water interfaces. They generate rotary and piston-like linear motion using specially designed, biologically based artificial muscles responsive to moisture fluctuations. Using these engines, we demonstrate an electricity generator that rests on water while harvesting its evaporation to power a light source, and a miniature car (weighing 0.1 kg) that moves forward as the water in the car evaporates. Evaporation-driven engines may find applications in powering robotic systems, sensors, devices and machinery that function in the natural environment.

42 ENGINEERING↗

DOE OSTI2017

Potential for natural evaporation as a reliable renewable energy resource

About 50% of the solar energy absorbed at the Earth’s surface drives evaporation, fueling the water cycle that affects various renewable energy resources, such as wind and hydropower. Recent advances demonstrate our nascent ability to convert evaporation energy into work, yet there is little understanding about the potential of this resource. Here in this paper we study the energy available from natural evaporation to predict the potential of this ubiquitous resource. We find that natural evaporation from open water surfaces could provide power densities comparable to current wind and solar technologies while cutting evaporative water losses by nearly half. We estimate up to 325 GW of power is potentially available in the United States. Strikingly, water’s large heat capacity is sufficient to control power output by storing excess energy when demand is low, thus reducing intermittency and improving reliability. Our findings motivate the improvement of materials and devices that convert energy from evaporation.

13 HYDRO ENERGY↗

DOE OSTI2025

Deuteron Evaporation from N = Z Compound Nuclei

Deuteron evaporation was observed from the N = Z compound nuclei 52 Fe ⋆ , 56 Ni ⋆ , and 64 Ge ⋆ in an experiment conducted at Argonne National Laboratory, USA. The experiment included a novel combination of two highly pixelated double-sided Si-strip detectors inside the Microball chargedparticle detection array, allowing for unequivocal discrimination of evaporated deuterons from protons and α particles. In conjunction with the Gammasphere array, Neutron Shell, and additional ancillary detectors, decay paths into various residual nuclei were investigated. The study provides insights into the competition of deuteron vs. proton-neutron evaporation as a function of available excitation energy and populated angular momentum. Results are interpreted using a statistical evaporation formalism for multiple subsequent particle emissions. The decisive factor in the comparison appears to be the available excitation energy in the residual system, with single nucleon evaporation preferred over deuteron evaporation for higher excitation energies.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

DOE OSTI2026

A dual membrane-adsorption evaporator for solar-powered lithium extraction from complex brines

A reliable supply of lithium is required to meet the increased demand for batteries over the coming decades. In this work, we demonstrated the potential to effectively extract lithium from brines by coupling solar-powered evaporation, adsorption, and membrane technologies together. We first synthesized a three-dimensional adsorptive evaporator by coating a lithium manganese oxide material onto a cotton stick using an easily scalable, one-step method. An osmotic membrane was then installed at the root of the evaporator to enhance the lithium to magnesium selectivity, prevent scaling caused by divalent cations, and thus further increase the water evaporation flux. The operation of the dual membrane-adsorption evaporator is entirely driven by osmosis and capillary force, demanding no extra energy input. The integration of the osmotic membrane was found to increase the lithium to magnesium selectivity over 10-fold to higher than 40. The dual process also produced high lithium to calcium selectivity and proved to sustain long-term stability by self-managing its internal osmotic pressure. Last, a test was done in three simulated brine solutions with varied brine chemistry and the evaporation rate stayed high and consistent throughout the long-term test. This illustrates that this technology can be used in varied brine solutions throughout the world providing efficient lithium capture and separation from competing divalent cations.

Eskafi, Aydin F. [University of California, Berkel↗

DOE OSTI2021

Minimizing Cr-Evaporation from Balance Of Plant Components By Utilizing Cost-Effective Alumina-Forming Austenitic Steels

A solid oxide fuel cell (SOFC) is a clean and efficient energy conversion device. The development of intermediate-temperature SOFCs has made it preferable to use metallic interconnects (MICs) to greatly reduce the cost and significantly increase the efficiency compared to ceramic interconnect materials. However, gaseous chromium species will evaporate from the chromium-containing layer formed on the surface of commonly used MICs and balance of plant (BoP) components. Volatile chromium species have been shown to form solid deposits which poison the cathodes of SOFCs, causing drastic cell performance degradation and thereby limiting commercialization. In order to alleviate the Cr poisoning and achieve long-term high performance of SOFC stacks, various Al 2 O 3 -forming austenitic (AFA) stainless steels applied at different temperatures are evaluated in this project. Based on our Phase I results (500 h operation), it is shown that on the AFAs, an alumina-based protective layer forms under high temperature that is invulnerable to water vapor effects and suppresses the diffusion of chromium and manganese which can prevent the generation of spinels on the alloy surface. Therefore, 310S, OC4 and OC5 at 800 °C and 625, OC11 and OC11LZ at 900 °C are selected to be tested in the Phase II long-term operation. From the results, we find that besides the lower Cr evaporation rates and better oxidation resistance of AFAs than benchmark alloys after short-term (500 h) operation, AFAs also possess the sturdy and compact alumina layer after a long-term operation (5000 h). A protective oxide layer is of great importance for the long-term high-temperature operation of structural materials. The high-temperature oxidation behavior of AFAs and commercial 310S and 625 alloys in Air + 10% H 2 O at 800 °C and 900 °C is systematically investigated. Severe breakaway oxidation and minor spallation are observed for the 310S and 625 after the long-term operation, while the AFAs show high oxidation resistance. It is found that the formation of a continuous alumina layer could greatly prevent the volatilization of chromium vapors. In addition, the corresponding evolving models are discussed. Chromium evaporation from BoP components in high-temperature environment could severely deteriorate the electrochemical performance of SOFC. Several methods were applied to evaluate the Cr evaporation rates of BoP after 500 h exposure at 800 °C to 900 °C in air with 10% H 2 O. An optimal method was designed to exclude the effect of silicon (Si) deposits from quartz tube and sodium (Na) deposits from the sodium carbonate on the oxidation process and the chemical interaction between Cr gaseous species and alumina tube which could provide further quantitative correlation of the evaporated Cr species quantities and degradation rates of SOFC. Based on the great performance of AFAs after long-term operation, AFAs are assembled with Anode-supported cells (ASC) to investigate the the Cr deposition of anode-supported cell under a constant current density of 0.5 A cm -2 at 800 °C with AFA alloys compared with commercial alloys. In addition, the anodic and cathodic processes are deconvoluted by distribution of relaxation times (DRT) method which are comprehensively discussed. It is found out that the voltage exhibited a slight decrease of 5.09 % and 1.54 % in the presence of OC11 and OC11LZA alloy, respectively. However, a considerable decrease of 22.14 % and 12.06 % was determined in the presence of 310S and 625 alloy, respectively. AFAs possessing the low-cost, low Cr evaporation rates and the high oxidation resistance will make it of great potential to replace the existing BoP components.

01 COAL, LIGNITE, AND PEAT↗

DOE OSTI2022

Characterization Results for the March 2022 Tank Farm 3H Evaporator Overhead Sample

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

DOE OSTI2024

Characterization Results for the September 2023 Tank Farm 3H Evaporator Overhead Sample

On an annual basis, Savannah River Mission Completion (SRMC) provides 2H and 3H evaporator overhead samples to Savannah River National Lab (SRNL) to be analyzed per Section 5.2 of the Effluent Treatment Project (ETP) Waste Compliance Plan (WCP) and the Waste Acceptance Criteria (WAC). This report presents the average characterization results for the September 2023 3H evaporator overhead sample. The sample was clear and colorless with no visible solids. The results provide measurements for cesium-137 ( 137 Cs), strontium-90 ( 90 Sr), and iodine-129 ( 129 I) with the radionuclide concentration limits specified by the WAC. These analyses were performed in duplicate, and all three measured radionuclide concentrations were within ETP WAC limits. A summary of the analytical results for this 3H evaporator overhead sample includes the following: The measured cesium-137 activity in the 3H evaporator overhead sample averaged 5.70E+01 dpm/mL, which is below the ETP WAC limit of 1.30E+03 dpm/mL. As seen through historical results, Cs-137 continues to present a decreasing activity since 2020. The strontium-90 activity in the 3H evaporator overhead sample averaged <2.16E00 dpm/mL, which is below the ETP WAC limit of 1.76E+02 dpm/mL. The iodine-129 activity in the 3H evaporator overhead sample averaged <9.08E-02 dpm/mL, which is below the ETP WAC limit of 1.00E+00 dpm/mL

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

DOE OSTI2024

Characterization Results for the October 2024 Tank Farm 3H Evaporator Overhead Sample

On an annual basis, Savannah River Mission Completion (SRMC) provides 2H and 3H evaporator overhead samples to Savannah River National Lab (SRNL) to be analyzed per Section 5.2 of the Effluent Treatment Project (ETP) Waste Compliance Plan (WCP) and the Waste Acceptance Criteria (WAC). This report presents characterization results for the October 2024 3H evaporator overhead sample. The sample was clear and colorless with no visible solids. The results provide measurements for cesium-137 (137Cs), strontium-90 (90Sr), and iodine-129 (129I) with the radionuclide concentration limits specified by the WAC. These analyses were performed in duplicate, and a summary of the analytical results for this 3H evaporator overhead sample includes the following: The measured cesium-137 activity in the 3H evaporator overhead sample averaged 6.72E+01 dpm/mL, (3.90E+00 %RSD), which is below the ETP WAC limit of 1.30E+03 dpm/mL. The strontium-90 activity in the 3H evaporator overhead sample averaged <2.72E+00 dpm/mL, which is below the ETP WAC limit of 1.76E+02 dpm/mL. The iodine-129 activity in the 3H evaporator overhead sample averaged <1.63E-01 dpm/mL, which is below the ETP WAC limit of 1.00E+00 dpm/mL.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

DOE OSTI2025

Characterization Results for the August 2025 Tank Farm 2H Evaporator Overhead Sample

On an annual basis, Savannah River Mission Completion (SRMC) provides 2H and 3H evaporator overhead samples to Savannah River National Lab (SRNL) to be analyzed per Section 5.2 of the Effluent Treatment Project (ETP) Waste Compliance Plan (WCP) and the Waste Acceptance Criteria (WAC). This report presents the average characterization results for the August 2025 2H evaporator overhead sample. The sample was clear and colorless with no visible solids. The results provide measurements for cesium-137 ( 137 Cs), strontium-90 ( 90 Sr), and iodine-129 ( 129 I) with the radionuclide concentration limits specified by the WAC. These analyses were performed in duplicate, and all three measured radionuclide concentrations were within ETP WAC limits. A summary of the analytical results for this 2H evaporator overhead sample includes the following: The measured cesium-137 activity in the 2H evaporator overhead sample averaged 3.02E+02 dpm/mL, which is below the ETP WAC limit of 1.30E+03 dpm/mL. The strontium-90 activity in the 2H evaporator overhead sample averaged 3.33E+00 dpm/mL, which is below the ETP WAC limit of 1.76E+02 dpm/mL. The iodine-129 activity in the 2H evaporator overhead sample averaged 1.20E-01 dpm/mL, which is below the ETP WAC limit of 1.00E+00 dpm/mL. Although the measurements for Cs-137 and Sr-90 are lower compared to previous years, the results remain within a similar range to past measurements and are well below the WAC limits. Iodine-129 indicates detectable results compared to previous years, which can be attributed to recent salt batch processing trending close to the WAC limit for saltstone production. However, these results are still below the ETP WAC limit.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

NASA NTRS1973

Evaporation rate and vapor pressure of selected polymeric lubricating oils.

A recently developed ultrahigh-vacuum quartz spring mass sorption microbalance has been utilized to measure the evaporation rates of several low-volatility polymeric lubricating oils at various temperatures. The evaporation rates are used to calculate the vapor pressures by the Langmuir equation. A method is presented to accurately estimate extended temperature range evaporation rate and vapor pressure data for polymeric oils, incorporating appropriate corrections for the increases in molecular weight and the change in volatility of the progressively evaporating polymer fractions. The logarithms of the calculated data appear to follow linear relationships within the test temperature ranges, when plotted versus 1000/T. These functions and the observed effusion characteristics of the fluids on progressive volatilization are useful in estimating evaporation rate and vapor pressure changes on evaporative depletion.

Gardos, M. N.↗