Showing posts with label analyser. Show all posts
Showing posts with label analyser. Show all posts

Friday, 29 May 2015

ATOMIC ABSORPTION SPECTROMETRY

INTRODUCTION

Atomic Absorption Spectrometry (AAS) is a technique which is used for the analysis of quantities of elements present in a sample by measuring the absorbed radiation by the chemical element of interest.
This is done by measuring the spectra produced when the sample is excited by radiation. The atoms absorb ultraviolet or visible light and get excited to higher energy levels. Atomic absorption technique measures the amount of energy in the form of photons of light that are absorbed by the sample.
A detector measures the wavelengths of light transmitted by the sample, and compares them to the wavelengths which originally passed through the sample. A signal processor then integrates the changes in wavelength absorbed, which appear in the readout as peaks of energy absorption at discrete wavelengths.

The energy required for an electron to leave an atom is known as ionization energy and is specific to each and every element. When an electron moves from one energy level to another within the atom, a photon is emitted with energy E. Atoms of an element emit a characteristic spectral line. Every atom has its own distinct pattern of wavelengths at which it will absorb energy, due to the unique configuration of electrons in its outer shell.
This enables the qualitative analysis of a sample. The concentration is calculated based on the Beer-Lambert law. Absorbance is directly proportional to the concentration of the analyte absorbed for the existing set of conditions. The concentration is usually determined from a calibration curve, obtained using standards of known concentration or certified reference materials (CRMs). However, applying the Beer-Lambert law directly in AAS is difficult due to:
·       variations in atomization efficiency from the sample matrix non-uniformity of concentration and path length of analyte atoms (in graphite furnace AA).

The chemical methods used are based on matter interactions, i.e. chemical reactions. For a long period of time these methods were essentially empirical, involving, in most cases, great experimental skills. In analytical chemistry, AAS is a technique used mostly for determining the concentration of a particular metal element within a sample. AAS can be used to analyse the concentration of over 62 different metals in a solution. Typically, the technique makes use of a flame to atomize the sample, but other atomizers, such as a graphite furnace, are also used. Three steps are involved in turning a liquid sample into an atomic gas:

1. Desolvation – the liquid solvent is evaporated, and the dry sample remains;
2. Vaporization – the solid sample vaporizes to a gas; and
3. Volatilization – the compounds that compose the sample are broken into free atoms.

To measure how much of a given element is present in a sample, first of all , we must establish a basis for comparison using certified reference materials or known quantities of that element to produce a calibration curve.
To generate this curve, a specific wavelength is selected, and the detector (Usually Photomultiplier tube detectors are used) is set to measure only the energy transmitted at that wavelength. As the concentration of the target atom in the sample increases, the absorption will also increase proportionally.

A series of samples containing known concentrations of the element to be measured are analysed, and the corresponding absorbance, which is the inverse percentage of light transmitted, is recorded.

The measured absorption at each concentration is then plotted, so that a straight line can then be drawn between the resulting points. From this line, the concentration of the substance under investigation is extrapolated from the substance’s absorbance. The use of special light sources and the selection of specific wavelengths allow for the quantitative determination of individual components in a multi-element mixture.

BASIC PRINCIPLE

The selectivity in AAS is very important, since each element has a different set of energy levels and gives rise to very narrow absorption lines. Hence, the selection of the monochromator is vital to obtain a linear calibration curve (Beers' Law), the bandwidth of the absorbing species must be broader than that of the light source; which is difficult to achieve with ordinary monochromators. The monochromator is a very important part of an AA spectrometer because it is used to separate the thousands of lines generated by all of the elements in a sample.

Without a good monochromator, detection limits are severely compromised. A monochromator is used to select the specific wavelength of light that is absorbed by the sample and to exclude other wavelengths. The selection of the specific wavelength of light allows for the determination of the specific element of interest when it is in the presence of other elements. The light selected by the monochromator is directed onto a detector,typically a photomultiplier tube, whose function is to convert the light signal into an electrical signal proportional to the light intensity. The challenge of requiring the bandwidth of the absorbing species to be broader than that of the light source is solved with radiation sources with very narrow lines.

The study of trace metals in wet and dry precipitation has increased in recent decades because trace metals have adverse environmental and human health effects. Some metals, such as Pb, Cd and Hg, accumulate in the biosphere and can be toxic to living systems.
Anthropogenic activities have substantially increased trace metal concentrations in the atmosphere. In addition, acid precipitation promotes the dissolution of many trace metals, which enhances their bioavailability. In recent decades, heavy metal concentrations have increased not only in the atmosphere but also in pluvial precipitation. Metals, such as Pb, Cd, As, and Hg, are known to accumulate in the biosphere and to be dangerous for living organisms, even at very low levels. Many human activities play a major role in global and regional trace element budgets. Additionally, when present above certain concentration levels, trace metals are potentially toxic to marine and terrestrial life. Thus, biogeochemical
perturbations are a matter of crucial interest in science.

The atmospheric input of metals exhibits strong temporal and spatial variability due to short atmospheric residence times and meteorological factors. As in oceanic chemistry, the impact of trace metals in atmospheric deposition cannot be determined from a simple consideration of global mass balance; rather, accurate data on net air or sea fluxes for specific regions are needed.

Particles in urban areas represent one of the most significant atmospheric pollution problems, and are responsible for decreased visibility and other effects on public health, particularly when their aerodynamic diameters are smaller than 10 μm, because these small particles can penetrate deep into the human respiratory tract. There have been many studies measuring concentrations of toxic metals such as Ag, As, Cd, Cr, Cu, Hg, Ni, Pb in rainwater and their deposition into surface waters and on soils. Natural sources of aerosols include terrestrial dust, marine aerosols, volcanic emissions and forest fires. Anthropogenic particles, on the other hand, are created by industrial processes, fossil fuel combustion, automobile mufflers, worn engine parts, and corrosion of metallic parts. The presence of metals in atmospheric particles are directly associated with health risks of these metals. Anthropogenic sources have substantially increased trace metal concentrations in atmospheric deposition.

The instrument used for atomic absorption spectrometry can have either of two atomizers. One attachment is a flame burner, which uses acetylene and air fuels. The second attachment consists of a graphite furnace that is used for trace metal analysis. Figure 1 depicts a diagram of an atomic absorption spectrometer.



Fig. 1. The spectral, or wavelength, range captures the dispersion of the grating across the linear array.
           
 Flame and furnace spectroscopy has been used for years for the analysis of metals. Today these procedures are used more than ever in materials and environmental applications. This is due to the need for lower detection limits and for trace analysis in a wide range ofsamples. Because of the scientific advances of Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), Inductively Coupled Plasma Mass Spectrometry (ICP-MS), have left Atomic Absorption (AA) behind. This technique, however, is excellent and has a larger specificity that ICP does not have.

Figure 2 shows a diagram of an atomic absorption spectrometer with a graphite furnace.


 AAS is a reliable chemical technique to analyze almost any type of material. This post describes the basic principles of atomic absorption spectroscopy in the analysis of trace metals, such as Ag, As, Cd, Cr, Cu, and Hg, in environmental samples. For example, the study of trace metals in wet and dry precipitation has increased in recent decades because trace metals have adverse environmental and human health effects. Anthropogenic activities have substantially increased trace metal concentrations in the atmosphere. In recent decades, heavy metal concentrations have increased not only in the atmosphere but also in pluvial precipitation.
Many human activities play a major role in global and regional trace element budgets. Additionally, when present above certain concentration levels, trace metals are potentially toxic to marine and terrestrial life. Thus, biogeochemical perturbations are a matter of crucial interest in science.
The atmospheric input of metals exhibits strong temporal and spatial variability due to short atmospheric residence times and meteorological factors. As in oceanic chemistry, the impact of trace metals in atmospheric deposition cannot be determined from a simple consideration of global mass balance; rather, accurate data on net air or sea fluxes for specific regions are needed.

Particles in urban areas represent one of the most significant atmospheric pollution
problems, and are responsible for decreased visibility and other effects on public health, particularly when their aerodynamic diameters are smaller than 10 μm, because these small particles can penetrate deep into the human respiratory tract. There have been many studies measuring concentrations of toxic metals such as Ag, As, Cd, Cr, Cu, Hg, Ni, Pb in rainwater and their deposition into surface waters and on soils. Natural sources of aerosols include terrestrial dust, marine aerosols, volcanic emissions and forest fires. Anthropogenic particles, on the other hand, are created by industrial processes, fossil fuel combustion, automobile mufflers, worn engine parts, and corrosion of metallic parts. The presence of metals in atmospheric particles and the associated health risks of these metals.

Anthropogenic sources have substantially increased trace metal concentrations in
atmospheric deposition. In addition, acid precipitation favors the dissolution of many trace metals, which enhances their bioavailability. Trace metals from the atmosphere are deposited by rain, snow and dry fallout. The predominant processes of deposition by rain are rainout and washout (scavenging). Generally, in over 80 % of wet precipitation, heavy metals are dissolved in rainwater and can thus reach and be taken up by the vegetation blanket and soils. Light of a specific wavelength, selected appropriately for the element being analyzed, is given off when the metal is ionized in the flame; the absorption of this light by the element of interest is proportional to the concentration of that element.

Quantification is achieved by preparing standards of the element.
  • AAS intrinsically more sensitive than Atomic Emission Spectrometry (AES)
  • Similar atomization techniques to AES
  • Addition of radiation source
  • High temperature for atomization necessary
  • Flame and electrothermal atomization
  • Very high temperature for excitation not necessary; generally no plasma/arc/spark in AAS

We will discuss the Flame AAS technique and AAS with Graphite Furnace (GFAA) in the upcoming posts.

Thursday, 2 January 2014

BREATH ALCOHOL ANALYSER

INTRODUCTION

Many humans are addicted to the psychoactive effects of alcohol thus, it is the most common, legal drug of choice. However, the influence of alcohol or the over-consumption of alcoholic drinks by humans is often the cause of crimes and violence, including fatal traffic accidents. Traffic deaths rank highest among all causes of death & alcohol related traffic fatalities rank highest within this category. Safety Agencies are challenged to locate intoxicated drivers and to remove them from the public roadways.
The analysis of alcohol in breath was considered a very desired and objective test specimen for determination of a vehicle operator’s breath-alcohol concentration and impairment level for evidential purposes. In the early 1950s, first Breathalyzer set the basis for the scientific acceptance of analyzing alcohol in breath. Law-Enforcement personnel implemented and administered these noninvasive and efficient tests as part of their drunk-driving enforcement.

THE TECHNOLOGY OF BREATH-ALCOHOL TESTING

The technology of breath-alcohol testing has changed fundamentally over the years. This was partially driven by general technology advancements and in part due to defense challenges. The following techniques describing the most recognized technologies used for preliminary (“screening”) and evidentiary breath-alcohol analysis as well as its advantages and disadvantages:

1. Wet-chemical Oxidation technology: 

The analytical principle was based on chemical oxidation by alcohol within a mixture of dichromate and sulfuric acid in vials. It paved the way for scientific acceptance of evidential breath alcohol testing by the international forensic community and the courts.

Advantages:
  • Compact table-top package.
  • Relatively quick analysis.
  • Accurate and specific to alcohol.


Disadvantage:
  • Minimum required breath volume < 60mL.
  • The handling of the vials is critical as they contain sulfuric acid.
  • The Breathalyzer’s biggest short-coming however, was the fact that the system was operator dependent.
  • Growing legal attacks in the eighties were vulnerable to manipulation by the operator thus; the equipment was rapidly replaced by newer and less operator dependent instruments.
 2Solid-state sensor technology:

Commonly called “Taguchi” cells, a metal oxide semiconductor based sensor manufactured by Figaro located in Japan. The Taguchi cell operates by adsorption of gas molecules on the surface of a semi-conductor. This transfers electrons due to the differing energy levels of the gas molecules on the semi-conductor’s surface. These types of instruments are sold mainly to the consumer markets as opposed to law enforcement. None of these sensor-type instruments are approved by the National Highway Safety Administration as evidential breath testers.

Advantages:
  • The sensors are small in size and rather inexpensive to manufacture. Lowest priced breath testers.
  • These instruments are sold in convenience stores and mail-order-catalogues.
Disadvantages:
  •  The sensor is very unstable, drifty and non-specific to alcohol.
  •  It reads all hydrocarbons (organic vapors) and will habitually produce false positive alcohol readings caused by smoker’s and car exhaust CO as well as many other environmental vapors and gases.
  • This senor is partial pressure sensitive and therefore changes sensitivity with change in altitude and elevation.
  • This sensor is sensitive to changes in ambient temperature, humidity and breath flow patterns.
  • For these and other reasons, solid-state sensor instruments can’t be employed in evidential and legal applications.
3. Electro-chemical cell technology (“EC”):

Most commonly called “fuel-cell”. Fuel-cell technology for alcohol analysis was first introduced in the early 1970s by an Austrian researcher. The EC sensor requires a sampling system consisting of a piston or bellow pump assembly, applying a very precise amount (~ 1 ccm) of breath to the sensor. The volume consistency is highly important because the current produced by the sensor is proportional to the total number of alcohol molecules converted in the sensor.
 The sensor is composed of an immobilized electrolyte, flanked by an active and a passive electrode. The electrolyte and the electrode material are selected such that the alcohol to be measured is electrochemically oxidized and converted at the active electrode. The change in the electronic conductivity causes a rise in current flowing from the active to the passive electrode. The total electrochemical reaction is evaluated by time integration of the sensor’s current. This sensor’s life expectancy is approximately 4-5 years.

Advantages:
  • The sensor is highly specific to alcohol.
  • The measurement cannot be biased or influenced by endogenous substances such as acetone (diabetics and starving people), CO or Toluene.
  • The sensor is highly sensitive, down to 0.1 ppm.
  • Accuracy meets specifications for evidential instruments (NHTSA) and remains stable ≥ 6 months before having to calibrate it again.
  • Its expected life term is approximately 5 years.
 Disadvantages:
  • EC based instruments cannot observe the breath alcohol concentration throughout the subject’s exhalation . This doesn’t allow detection of alveolar breath (“deep lung air”), mouth alcohol, belching, burping, Gastro Esophageal Reflux Disease (GERD) and residual alcohol trapped under dentures or alcohol from bleeding gums.
  • The EC sensor is cross sensitive to other alcohols such as methanol and isopropanol.The EC sensor’s output is temperature dependent and suffers short term fatigue if the sensor is exposed to a series of successive alcohol containing tests.
  • EC based instruments are not accepted for evidential use in many countries, states and jurisdictions.
4. Infrared Spectroscopy (“IR”):

IR technology (IR Spectra-photometry) based breath-alcohol testers were first introduced in the mid-1970s. IR instruments have become the standard worldwide for legal, evidential breath analysis.
The analytical concept is based on the Beer-Lambert Law of physics, the “Law of absorption”. It addresses the linear relationship between absorbance and concentration of an absorber of  electromagnetic radiation. Alcohol vapor introduced into an absorption chamber will absorb some of that IR radiation transmitted through the chamber. The amount of IR absorption is in direct proportion to the quantity of alcohol present (breath-alcohol). However, only IR-radiation of a specific wavelength will absorb alcohol. The two predominantly utilized wavelengths are centered at 3.39 and 9.5 μm. The latest generation instrumentation monitors IR absorption at 9.5 μm because the measurements are far less prone to interference from any hydrocarbons and acetone which absorb IR energy at 3.4 μm.

The most significant benefits of “real-time” IR absorption analysis (continuous measurement) requires understanding the dynamics of alcohol in the human breath. Some of these dynamics relate to gas exchange in the mucus membranes, residual alcohol in the upper respiratory tracks, belching, burping, Gastro Esophageal Reflux Disease (GERD), exhaled air volume, breath flow rates and the subject’s breathing pattern.

Only IR technology is capable of addressing these dynamic, physiological factors to determine a legitimate, rightful and legally as well as forensically justifiable breath alcohol measurement.

Advantages:
  • IR based equipment observes the breath-alcohol concentration throughout the subject’s exhalation. This allows the plot of the entire IR-absorption curve and the instrument’s intelligence to assure that.
  • The breath sample was of alveolar nature.
  • No residual or mouth alcohol was present.
  • The recorded absorption curve can be presented in court if the case is challenged.
  • The IR system does not have a limited life expectancy, will not fatigue with successive, high alcohol concentration test series and remains extremely stable for years.
  • These instruments are equipped with many other important peripherals and functionalities (please observe “Other required performance features for evidential breath testers” below).
  • IR instruments are today’s standard worldwide for legal, evidential breath-alcohol analysis and consequently face fewer legal challenges than all other breath testing devices and technologies. 
Disadvantages: 
  • IR instruments are larger in size thus, not suitable for portable, handheld operation.
  • These instruments are more expensive than handheld (screening) equipment employing solid-state or EC sensors.


Various human specimens can be considered for measuring a person’s alcohol concentration level. All body fluids as well as expired breath are legitimate specimens for alcohol concentration measurements. However, the two most popular methodologies for medico legal alcohol testing are blood analysis and breath analysis.


Roadside tests or so called screening tests are conducted with handheld, mainly EC based instruments. These instruments are portable, battery operated and provide quick test results.The main objective of these tests are for confirmation of probable cause for submission to an evidential test procedure.