Index of Chemical Agent Detectors and Supplies and Manufacturers

2004 ◽  
pp. 249-250
Keyword(s):  
Chemical Agent

Atom-probe analysis of the solid-liquid interface

1995 ◽  
Vol 53 ◽  
pp. 676-677
Author(s):  
J.A. Panitz
Keyword(s):  
Molecular Level ◽  
Selective Adsorption ◽  
Electronic Devices ◽  
Atom Probe ◽  
Chemical Agent ◽  
Hostile Environment ◽  
Solid Interface ◽  
Solid Liquid Interface ◽  
Solid Liquid ◽  
Chemically Selective

The first few atomic layers of a solid can form a barrier between its interior and an often hostile environment. Although adsorption at the vacuum-solid interface has been studied in great detail, little is known about adsorption at the liquid-solid interface. Adsorption at a liquid-solid interface is of intrinsic interest, and is of technological importance because it provides a way to coat a surface with monolayer or multilayer structures. A pinhole free monolayer (with a reasonable dielectric constant) could lead to the development of nanoscale capacitors with unique characteristics and lithographic resists that surpass the resolution of their conventional counterparts. Chemically selective adsorption is of particular interest because it can be used to passivate a surface from external modification or change the wear and the lubrication properties of a surface to reflect new and useful properties. Immunochemical adsorption could be used to fabricate novel molecular electronic devices or to construct small, “smart”, unobtrusive sensors with the potential to detect a wide variety of preselected species at the molecular level. These might include a particular carcinogen in the environment, a specific type of explosive, a chemical agent, a virus, or even a tumor in the human body.

Single Cell Based Microelectrode Array Biosensors

2003 ◽  
Vol 773 ◽  
Author(s):  
Mo Yang ◽  
Shalini Prasad ◽  
Xuan Zhang ◽  
Mihrimah Ozkan ◽  
Cengiz S. Ozkan
Keyword(s):  
Electrical Activity ◽  
Single Cell ◽  
Cellular Response ◽  
Microelectrode Array ◽  
Fast Fourier Transformation ◽  
Chemical Agent ◽  
Extracellular Potential ◽  
Membrane Excitability ◽  
Specific Chemical ◽  
Chemical Agents

AbstractExtracellular potential is an important parameter which indicates the electrical activity of live cells. Membrane excitability in osteoblasts plays a key role in modulating the electrical activity in the presence of chemical agents. The complexity of cell signal makes interpretation of the cellular response to a chemical agent very difficult. By analyzing shifts in the signal power spectrum, it is possible to determine a frequency spectrum also known as Signature Pattern Vectors (SPV) specific to a chemical. It is also essential to characterize single cell sensitivity and response time for specific chemical agents for developing detect-to-warn biosensors. We used a 4x4 multiple Pt microelectrode array to spatially position single osteoblast cells, by using a gradient AC field. Fast Fourier Transformation (FFT) and Wavelet Transformation (WT) analyses were used to extract information pertaining to the frequency of firing from the extracellular potential.

Removal of copper (Cu2+) by preparation modified carbon from macadamia shells by chemical agent with H2O2 in wastewater

2020 ◽  
pp. 215-221
Keyword(s):  
Heavy Metal ◽  
Processing Time ◽  
Chemical Agent ◽  
Optimum Conditions ◽  
Adsorption Ability

Macadamia shells were used to prepare modified carbon by chemical agent H2O2 (25%) in 48 hours with coke ratio: H2O2 = 1:10. Modified carbon from Macadamia shells with chemical agent H2O2 has capable of adsorption heavy metal copper (Cu 2+) at an assumption concentration is 30ppm in the optimum conditions such as pH = 4, dose is 1.8 g/l, and the processing time is 30 minutes. The result showed that the adsorption ability of the material reached the highest efficiency is 78.33%. This result showed that modified carbon from shells Macadamia by chemical agent H2O2 capable of removing applications on heavy metal copper (Cu2+) in wastewater.

Chemical Stockpile Disposal Program. Chemical Agent and Munition Disposal. Summary of the U.S. Army's Experience

1987 ◽  
Author(s):  
Kevin J. Flamm ◽  
Quon Kwan ◽  
William B. McNulty
Keyword(s):  
Chemical Agent ◽  
The U.S

Thermal Modeling of Biological Mustard Hydrolysate Treatment Reactors and Full-Scale Simulated Testing at the Pueblo Chemical Agent-Destruction Pilot Plant

2015 ◽  
Vol 2015 (6) ◽  
pp. 5907-5927
Author(s):  
Paul J Usinowicz ◽  
George Lecakes ◽  
Thomas C Spear ◽  
Zack Burger ◽  
Charles Oclassen ◽  
...  
Keyword(s):  
Pilot Plant ◽  
Thermal Modeling ◽  
Full Scale ◽  
Chemical Agent

Disaster Preparedness: Hospital Decontamination and the Pediatric Patient— Guidelines for Hospitals and Emergency Planners

2008 ◽  
Vol 23 (2) ◽  
pp. 166-173 ◽  
Author(s):  
Christopher W. Freyberg ◽  
Bonnie Arquilla ◽  
Baruch S. Fertel ◽  
Michael G. Tunik ◽  
Arthur Cooper ◽  
...  
Keyword(s):  
New York ◽  
Disaster Preparedness ◽  
Mental Hygiene ◽  
Emergency Situation ◽  
Chemical Agent ◽  
Hospital Emergency ◽  
Department Of Health ◽  
Policies And Procedures ◽  
Patient Guidelines ◽  
Hospital Emergency Departments

AbstractIn recent years, attention has been given to disaster preparedness for first responders and first receivers (hospitals). One such focus involves the decontamination of individuals who have fallen victim to a chemical agent from an attack or an accident involving hazardous materials. Children often are overlooked in disaster planning. Children are vulnerable and have specific medical and psychological requirements. There is a need to develop specific protocols to address pediatric patients who require decontamination at the entrance of hospital emergency departments. Currently, there are no published resources that meet this need. An expert panel convened by the New York City Department of Health and Mental Hygiene developed policies and procedures for the decontamination of pediatric patients.The panel was comprised of experts from a variety of medical and psychosocial areas.Using an iterative process, the panel created guidelines that were approved by the stakeholders and are presented in this paper.These guidelines must be utilized, studied, and modified to increase the likelihood that they will work during an emergency situation.

Crystal Violet, an Electronic Model Substance for Rubber and Related Olefins

1951 ◽  
Vol 24 (1) ◽  
pp. 169-181 ◽  
Author(s):  
G. J. van Veersen
Keyword(s):  
Crystal Violet ◽  
Electronic Structures ◽  
Radical Reaction ◽  
Test Tube ◽  
Chemical Agent ◽  
Blue Color ◽  
Electronic Model ◽  
Model Substance ◽  
Model Substances ◽  
Polar Reaction

Abstract It is shown that triphenylmethyl dyes like crystal violet can be used as model substances for rubber and related olefins. Arguments are given in support of the assumption that agents which react with rubber and related olefins in a polar manner cause a reversible shift in color from blue to yellow with crystal violet, whereas a fading of the blue color of crystal violet (if alkaline or reducing agents are excluded) points to a radical reaction. Since the electronic structures of donor olefins and crystal violet are considered and not the molecular structure, as usually is done in the choice of a model substance, these dyes have been named electronic model substances. Though crystal violet, as an electronic model substance cannot be used for the study of the overall reactions, information can often be obtained concerning the first step in a reaction of rubber with a certain chemical agent by means of a simple test-tube reaction with crystal violet. It was pointed out that the π-electron availability at the non-methylated carbon atom of the double bond in rubber and at the nitrogen atoms in crystal violet is probably of the same order. As an application of crystal violet as an electronic model substance for rubber, a polar reaction between sulfur and rubber is suggested as the first step in vulcanization.

scholarly journals Early Detection of Exposure to Toxic Chemicals Using Continuously Recorded Multi-Sensor Physiology

Sensors ◽  
2021 ◽  
Vol 21 (11) ◽  
pp. 3616
Author(s):  
Jan Ubbo van Baardewijk ◽  
Sarthak Agarwal ◽  
Alex S. Cornelissen ◽  
Marloes J. A. Joosen ◽  
Jiska Kentrop ◽  
...  
Keyword(s):  
Machine Learning ◽  
Early Detection ◽  
Physiological Signals ◽  
Machine Learning Techniques ◽  
Detection Accuracy ◽  
Chemical Agent ◽  
Counter Measures ◽  
Detection And Identification ◽  
Life Saving ◽  
Future Work

Early detection of exposure to a toxic chemical, e.g., in a military context, can be life-saving. We propose to use machine learning techniques and multiple continuously measured physiological signals to detect exposure, and to identify the chemical agent. Such detection and identification could be used to alert individuals to take appropriate medical counter measures in time. As a first step, we evaluated whether exposure to an opioid (fentanyl) or a nerve agent (VX) could be detected in freely moving guinea pigs using features from respiration, electrocardiography (ECG) and electroencephalography (EEG), where machine learning models were trained and tested on different sets (across subject classification). Results showed this to be possible with close to perfect accuracy, where respiratory features were most relevant. Exposure detection accuracy rose steeply to over 95% correct during the first five minutes after exposure. Additional models were trained to correctly classify an exposed state as being induced either by fentanyl or VX. This was possible with an accuracy of almost 95%, where EEG features proved to be most relevant. Exposure detection models that were trained on subsets of animals generalized to subsets of animals that were exposed to other dosages of different chemicals. While future work is required to validate the principle in other species and to assess the robustness of the approach under different, realistic circumstances, our results indicate that utilizing different continuously measured physiological signals for early detection and identification of toxic agents is promising.

scholarly journals Deciphering the Disaggregation Mechanism of Amyloid Beta Aggregate by 4-(2-Hydroxyethyl)-1-Piperazinepropanesulfonic Acid Using Electrochemical Impedance Spectroscopy

Sensors ◽  
2021 ◽  
Vol 21 (3) ◽  
pp. 788
Author(s):  
Hien T. Ngoc Le ◽  
Sungbo Cho
Keyword(s):  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Electrochemical Impedance ◽  
Specific Binding ◽  
Amyloid Β ◽  
Electrochemical Measurement ◽  
Charge Transfer Resistance ◽  
Chemical Agent ◽  
Transfer Resistance ◽  
K Value

Aggregation of amyloid-β (aβ) peptides into toxic oligomers, fibrils, and plaques is central in the molecular pathogenesis of Alzheimer’s disease (AD) and is the primary focus of AD diagnostics. Disaggregation or elimination of toxic aβ aggregates in patients is important for delaying the progression of neurodegenerative disorders in AD. Recently, 4-(2-hydroxyethyl)-1-piperazinepropanesulfonic acid (EPPS) was introduced as a chemical agent that binds with toxic aβ aggregates and transforms them into monomers to reduce the negative effects of aβ aggregates in the brain. However, the mechanism of aβ disaggregation by EPPS has not yet been completely clarified. In this study, an electrochemical impedimetric immunosensor for aβ diagnostics was developed by immobilizing a specific anti-amyloid-β (aβ) antibody onto a self-assembled monolayer functionalized with a new interdigitated chain-shaped electrode (anti-aβ/SAM/ICE). To investigate the ability of EPPS in recognizing AD by extricating aβ aggregation, commercially available aβ aggregates (aβagg) were used. Electrochemical impedance spectroscopy was used to probe the changes in charge transfer resistance (Rct) of the immunosensor after the specific binding of biosensor with aβagg. The subsequent incubation of the aβagg complex with a specific concentration of EPPS at different time intervals divulged AD progression. The decline in the Rct of the immunosensor started at 10 min of EPPS incubation and continued to decrease gradually from 20 min, indicating that the accumulation of aβagg on the surface of the anti-aβ/SAM/ICE sensor has been extricated. Here, the kinetic disaggregation rate k value of aβagg was found to be 0.038. This innovative study using electrochemical measurement to investigate the mechanism of aβagg disaggregation by EPPS could provide a new perspective in monitoring the disaggregation periods of aβagg from oligomeric to monomeric form, and then support for the prediction and handling AD symptoms at different stages after treatment by a drug, EPPS.

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