INDUCTIVE COUPLED PLASMA OPTICAL EMISSION SPECTROMETER.
ICP/OES is one of the most powerful and popular analytical tools for the determination of trace elements in a sample types. The technique is based upon the spontaneous emission of photons from atoms and ions that have been excited in a RF discharge. Liquid and gas samples may be injected directly into the instrument, while solid samples require extraction or acid digestion so that the analytes will be present in a solution. The sample solution is converted to an aerosol and directed into the central channel of the plasma. At its core the inductively coupled plasma (ICP) sustains a temperature of approximately 10 000 K, so the aerosol is quickly vaporized. Analyte elements are liberated as free atoms in the gaseous state. Further collisional excitation within the plasma imparts additional energy to the atoms, promoting them to excited states. Sufficient energy is often available to convert the atoms to ions and subsequently promote the ions to excited states. Both the atomic and ionic excited state species may then relax to the ground state via the emission of a photon. These photons have characteristic energies that are determined by the quantized energy level structure for the atoms or ions. Thus the wavelength of the photons can be used to identify the elements from which they originated. The total number of photons is directly proportional to the concentration of the originating element in the sample.The instrumentation associated with an ICP/OES system is relatively simple. A portion of the photons emitted by the ICP is collected with a lens or a concave mirror. This focusing optic forms an image of the ICP on the entrance aperture of a wavelength selection device such as a monochromator. The particular wavelength exiting the monochromator is converted to an electrical signal by a photo detector. The signal is amplified and processed by the detector electronics, then displayed and stored by a computer.
ICP OES OPERATION
The ICP is generated as follows. RF power, typically 700–1500 W, is applied to the load coil and an alternating current oscillates inside the coil at a rate corresponding to the frequency of the RF generator. For most ICP/OES instruments, the RF generator has a frequency of either 27 or 40 MHz. The oscillation of the current at this high frequency causes the same high-frequency oscillation of electric and magnetic fields to be set up inside the top of the torch. With argon gas flowing through the torch, a spark from a Tesla coil is used to produce ‘‘seed’’ electrons and ions in the argon gas inside the load coil region. These ions and electrons are then accelerated by the magnetic field, and collide with other argon atoms, causing further ionization in a chain reaction manner. This process continues until a very intense, brilliant white, tear drop shaped, high-temperature plasma is formed. Adding energy to the plasma viaRF-induced collision is known as inductive coupling, and thus the plasma is called an ICP. The ICP is sustained within the torch as long as sufficient RF energy is applied in a cruder sense, the coupling of RF power to the plasma can be visualized as positively charged Ar ions in the plasma gas attempting to follow the negatively charged electrons flowing in the load coil as the flow changes direction 27 million times per second. Figure shows the temperature gradient within the ICP with respect to height above the load coil. It also gives the nomenclature for the different zones of the plasma .The induction region at the base of the plasma is ‘‘doughnut-shaped’’ as described above, and it is the region where the inductive energy transfer occurs. This is also the region of highest temperature and it is characterized by a bright continuum emission. From the IR upward towards to the tail plume, the temperature decreases. An aerosol, or very fine mist of liquid droplets, is generated from a liquid sample by the use of a nebulizer. The aerosol is carried into the center of the plasma by the argon gas flow through the induction region. Upon entering the plasma, the droplets undergo three processes. The first step is desolvation, or the removal of the solvent from the droplets, resulting in microscopic solid particulates, or a dry aerosol. The second step is vaporization, or the decomposition of the particles into gaseous state molecules. The third step is atomization, or the breaking of the gaseous molecules into atoms. These steps occur predominantly in the preheating zone . Finally, excitation and ionization of the atoms occur, followed by the emission of radiation from these excited species. These excitation and ionization processes occur predominantly in the initial radiation zone, and the normal analytical zone from which analytical emission is usually collected.
ICP OES INSTRUMENTATION
In inductively coupled plasma-optical emission spectrometry, the sample is usually transported into the instrument as a stream of liquid sample. Inside the instrument,the liquid is converted into an aerosol through a process known as nebulization. The sample aerosol is then transported to the plasma where it is desolvated, vaporized, atomized, and excited and/or ionized by the plasma. The excited atoms and ions emit their characteristic radiation which is collected by a device that sorts the radiation by wavelength. The radiation is detected and turned into electronic signals that are converted into concentration information for the analyst. A representation of the layout of a typical ICP-OES instrument is shown in Figure.
|Major components and ICP-OES instrument|
A sample introduction system is used to transport a sample into the central channel of the ICP as either a gas, vapor, aerosol of fine droplets, or solid particles. The general requirements for an ideal sample introduction system include amenity to samples in all phases (solid, liquid, or gas), tolerance to complex matrices, the ability to analyse very small amount of samples (<1mL or <50 mg), excellent stability and reproducibility, high transport efficiency, simplicity, and low cost. A wide variety of sample introduction methods have been developed, such as nebulization, hydride generation (HG), electro thermal vaporization (ETV), and laser ablation.
1. CONCENTRIC NEBULIZER
The concentric nebulizer is fashioned from fused silica. Sample solution is pumped into the back end of the nebulizer by a peristaltic pump. Liquid uptake rates may be as high as 4mLmin, but lower flows are more common. The sample solution flows through the inner capillary of the nebulizer. This capillary is tapered so that flexible tubing from the pump is attached at the entrance (4mm outer diameter) and the exit has a narrow orifice approaching 100 mm or less in inner diameter. Ar gas (0.5–1.5 Lmin) is supplied at a right angle into the outer tube. This tube is also tapered so that the exit internal diameter approaches the outer diameter for the sample capillary. As the Ar passes through this narrow orifice, its velocity is greatly increased, resulting in the shearing of the sample stream into tiny droplets. Concentric nebulizers have the advantages of excellent sensitivity and stability, but the small fragile fused-silica orifices are prone to clogging, especially when aspirating samples of high salt content. Concentric nebulizers also require a fairly large volume of sample, given the high uptake rate. The microconcentric nebulizer (MCN) is designed to solve this problem. The sample uptake rate for the MCN is less than 0.1mLmin. The compact MCN employs a smaller diameter capillary (polyimide or TeflonÒ) and poly(vinylidine difluoride) body to minimize the formation of large droplets.
2. CROSS-FLOW NEBULIZER
A second type of pneumatic nebulizer is the cross-flow nebulizer, shown in Figure . The operation of cross-flow nebulizers is often compared to that of a perfume atomizer. Here a high speed stream of argon gas is directed perpendicular to the tip of a capillary tube (in contrast to the concentric or micro-concentric nebulizers where the high-speed gas is parallel to the capillary). The solution is either drawn up through the capillary tube by the low-pressure region created by the high-speed gas or forced up the tube with a pump. In either case, contact between the high-speed gas and the liquid stream causes the liquid to break up into an aerosol. Cross-flow nebulizers are generally not as efficient as concentric nebulizers at creating the small droplets needed for ICP analyses. However, the larger diameter liquid capillary and longer distance between liquid and gas injectors minimize clogging problems. Many analysts feel that the small penalty paid in analytical sensitivity is more than compensated for by the freedom from clogging. Another advantage of cross-flow nebulizers is that they are generally more rugged and corrosion-resistant than glass concentric nebulizers. In fact, this nebulizer is available with a Ryton body, a clear sapphire liquid capillary tip and a red ruby gas injector tip both contained in a polyetheretherketone (PEEK) body, all which provide chemical resistance to samples .
3. BABINGTON NEBULIZER
The third type of pneumatic nebulizer used for ICP/OES is the Babington nebulizer that allows a film of the sample solution to flow over a smooth surface having a small orifice . High-speed argon gas emanating from the hole shears the sheet of liquid into small droplets. The essential feature of this type of nebulizer is that the sample solution flows freely over a small aperture, rather than passing through a fine capillary, resulting in a high tolerance to dissolved solids In fact, even slurries can be nebulized with a Babington nebulizer. This type of nebulizer is the least susceptible to clogging and it can nebulize very viscous liquids.
Once the sample aerosol is created by the nebulizer, it must be transported to the torch so it can be injected into the plasma. Because only very small droplets in the aerosol are suitable for injection into the plasma, a spray chamber is placed between the nebulizer and the torch. Some typical ICP spray chamber designs are shown in Figure 3-10. The primary function of the spray chamber is to remove large droplets from the aerosol. A secondary purpose of the spray chamber is to smooth out pulses that occur during nebulization, often due to pumping of the solution. In general, spray chambers for the ICP are designed to allow droplets with diameters of about 10 mm or smaller to pass to the plasma. With typical nebulizers, this droplet range constitutes about 1 - 5% of the sample that is introduced to the nebulizer. The remaining 95 - 99% of the sample is drained into a waste container.
The material from which a spray chamber is constructed can be an important characteristic of a spray chamber. Spray chambers made from corrosion-resistant materials allow the analyst to introduce samples containing hydrofluoric acid which could damage glass spray chambers.
The torches used in ICP-OES are very similar in design and function to those in the early days of ICP-OES.As shown schematically in Figure, the torches contain three concentric tubes for argon flow and aerosol injection. The spacing between the two outer tubes is kept narrow so that the gas introduced between them emerges at high velocity. This outside chamber is also designed to make the gas spiral tangentially around the chamber as it proceeds upward. One of the functions of this gas is to keep the quartz walls of the torch cool and thus this gas flow was originally called the coolant flow or plasma flow but is now called the "outer" gas flow. For argon ICPs, the outer gas flow is usually about 7 - 15 liters per minute. The chamber between the outer flow and the inner flow sends gas directly under the plasma toroid. This flow keeps the plasma discharge away from the intermediate and injector tubes and makes sample aerosol introduction into the plasma easier. In normal operation of the torch, this flow, formerly called the auxiliary flow but now the intermediate gas flow, is about 1.0 L/min. The intermediate flow is usually introduced to reduce carbon formation on the tip of the injector tube when organic samples are being analyzed. However, it may also improve performance with aqueous samples as well. With some torch and sample introduction configurations, the intermediate flow may be as high as 2 or 3 L/min or not used at all. The gas flow that carries the sample aerosol is injected into the plasma through the central tube or injector. Due to the small diameter at the end of the injector, the gas velocity is such that even the 1 L/min of argon used for nebulization can punch a hole through the plasma. Since this flow carries the sample to the plasma, it is often called the sample or nebulizer flow but in present terminology, this flow is known as the inner gas flow. Furthermore, this flow acts as the carrier gas for solid aerosols from spark ablation and laser ablation sample introduction techniques.
RADIO FREQUENCY GENERATOR
RADIO FREQUENCY GENERATOR
The radio frequency (RF) generator is the device that provides the power for the generation and sustainment of the plasma discharge. This power, typically ranging from about 700 to 1500 watts, is transferred to the plasma gas through a load coil surrounding the top of the torch. The load coil, which acts as an antenna to transfer the RF power to the plasma, is usually made from copper tubing and is cooled by water or gas during operation.Most RF generators used for ICP-OES operate at a frequency between 27 and 56 MHz, most ICP generators were operated at 27.12 MHz. However, an increasing number of instruments now operate at 40.68 MHz because of improvements in coupling efficiency and reductions in background emission intensity realized at this frequency. Frequencies greater than 40 MHz also have been used but have not been as successful commercially. There are two general types of RF generators used in ICP instruments. Crystal-controlled generators use a piezoelectric quartz crystal to produce an RF oscillating signal that is amplified by the generator before it is applied at the load coil. The proper electrical parameters, such as output impedance, needed to keep the generator operating efficiently are controlled by a matching network that utilizes manual or automatic (servo mechanical) components. The speed and accuracy of this matching network are critical to the operation of this type of generator.
DETECTION OF EMISSION
DETECTION OF EMISSION
Most of the analytically useful emission lines for ICP-OES are in the 190 - 450 nm region; thus, spectrometers used for ICP-OES are usually optimized for operation in this wavelength region. However, there are also some important ICP emission lines between 160 and 190 nm and above 450 nm. Unfortunately, electromagnetic radiation in the 160 - 190 nm wavelength region is readily absorbed by oxygen molecules, and instruments must be specially designed to remove the air from the spectrometer to observe emission in this wavelength region. Removing oxygen from the spectrometer is done either by purging the spectrometer with a gas, usually nitrogen or argon, that doesn’t absorb the emission, or by removing the air from the spectrometer with a vacuum system. Recently, nitrogen filled optics maintained at atmospheric pressure and incorporating a catalyst for scrubbing the recycled nitrogen have been introduced.
1. PMT DETECTOR
Once the proper emission line has been isolated by the spectrometer, the detector and its associated electronics are used to measure the intensity of the emission line. By far the most widely used detector for ICP-OES is the photomultiplier tube or PMT. To know more about the PMT read the topic Photomultiplier Tube.
2. ARRAY CCD DETECTOR
Charge transfer devices include a broad range of solid-state silicon-based array detectors. They include the charge injection device (CID) and the charge-coupled device (CCD). The CCD has found extensive use in nonspectroscopic devices such as video cameras, bar code scanners, and photocopiers. With the CTDs, photons falling on a silicon substrate produce electron–hole pairs.The positive electron holes migrate freely through the p type silicon semiconductor material, while the electrons are collected and stored temporarily by an array of metal oxide semiconductor (MOS) capacitors The CCD differs from the CID mainly in the readout scheme. The CCD is read out in a sequential charge shifting manner towards the output amplifier. The CID on the other hand may be read out in a non-destructive manner by shifting charge between adjacent electrodes, and then shifting it back again. The CID thus benefits from quick random access, even during long integration periods. Spectroscopic applications of CTD’s has been hampered by the physical mismatch between the relatively small surface area of the detector and the large sometimes two dimensional focal plane associated with polychromators. This mismatch may be overcome, however, and one commercial ICP spectrometer employs a CID detector having more than 250 000 pixels positioned upon an echelle focal plane. Alternative approaches have been successful with the CCD detector. In one case, a group of several CCD arrays are arranged around a Circular Optical System (CIROS) based upon a Rowland circle design. Rather than monitoring discrete wavelengths as is the case with the multiple PMT Rowland circle systems, the CIROS system provides total wavelength coverage from 120 to 800 nm, with resolution on the order of 0.009 nm
HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY
High-performance liquid chromatography (sometimes referred to as high-pressure liquid chromatography), HPLC, is a chromatographic technique used to separate a mixture of compounds in analytical chemistry and biochemistry with the purpose of identifying, quantifying or purifying the individual components of the mixture.
|Basic block diagram|
HPLC is accomplished by injection of a small amount of liquid sample into a moving stream of liquid (called the mobile phase) that passes through a column packed with particles of stationary phase. Separation of a mixture into its components depends on different degrees of retention of each component in the column. The extent to which a component is retained in the column is determined by its partitioning between the liquid mobile phase and the stationary phase. In HPLC this partitioning is affected by the relative solute/stationary phase and solute/mobile phase interactions. Thus, unlike GC, changes in mobile phase composition can have an enormous impact on your separation. Since the compounds have different mobilities, they exit the column at different times; i.e., they have different retention times, tR. The retention time is the time between injection and detection. There are numerous detectors which can be used in liquid chromatography. It is a device that senses the presence of components different from the liquid mobile phase and converts that information to an electrical signal. For qualitative identification one must rely on matching retention times of known compounds with the retention times of components in the unknown mixture.Quantitative analysis is often accomplished with HPLC. An automatic injector providing reproducible injection volumes is extremely beneficial, and are standard on modern commercial systems.
HPLC is just one type of liquid chromatography, meaning the mobile phase is a liquid. In this lab you will use what is called reversed phase HPLC. Reversed phase HPLC is the most common type of HPLC. What reversed phase means is that the mobile phase is relatively polar, and the stationary phase is relatively non-polar. Thus non-polar compounds will be more retained (i.e. Have longer retention times) than a polar compound. In normal phase HPLC, the mobile phase is relatively non-polar and the stationary phase is relatively polar. Other more general types of HPLC include partition, adsorption, ion-exchange, size-exclusion, and thin-layer chromatography.
- Quantitative/qualitative analyses of amino acids, nucleic acids, proteins in physiological samples.
- Measuring levels of active drugs, synthetic by-products, degradation products in pharmaceuticals.
- Measuring levels of hazardous compounds such as pesticides and insecticides.
- Monitoring environmental samples.
- Purifying compounds from mixtures.
LASER PARTICLE COUNTER
A particle counter is an instrument that detects and counts particles. By its very nature a particle counter is a single particle counter, meaning it detects and counts particles one at a time. The nature of particle counting is based upon either light scattering, light obscuration, or direct imaging. A high energy light source is used to illuminate the particle as it passes through the detection chamber. The particle passes through the light source (typically a laser or halogen light) and if light scattering is used, then the redirected light is detected by a photo detector. If direct imaging is used, a halogen light illuminates particles from the back within a cell while a high definition, high magnification camera records passing particles. Recorded video is then analyzed by computer software to measure particle attributes. If light blocking (obscuration) is used the loss of light is detected. The amplitude of the light scattered or light blocked is measured and the particle is counted and tabulated into standardized counting bins.
|The laser beam passes through the walls of a glass container or a flow-thru cell|
Particle counter uses as its basic light source a laser diode (650nm wavelength). The beam from this laser is spatially filtered and focused by a lens assembly to form a small and well-defined illuminated volume within the liquid being inspected. A scanning mechanism provides a circular displacement of this illuminated volume at a constant rate of speed. As the illuminated volume moves across a particle suspended in the liquid, some light from the beam will be scattered. This is known as Fraunhofer diffraction. Most of this scattered light is in the near-forward direction and is collected by the optical system of the photodetector assembly. The flash of light striking the photodetector will cause an electrical pulse in the preamplifier connected to the photodetector. The amplitude and width of this pulse are a function of the size of the particles, The analog signals generated by the light pulses are routed to a computer and digitized.
- Quality control of hydraulic fluids and oils.
- De-ionized water and acid testing for semiconductor manufacturing.
- Vial and ampule inspection for pharmaceuticals.
- Silt and sediment sizing.
- Oceanographic particles.
- Sizing for corrosive chemicals and solvents.
- Cell counting where physical force would damage particles.
- Particle agglomeration studies.
- Water treatment plants.
- Filter efficiency control.
- Powdered solids manufacturing.
Fourier Transform-Infrared Spectroscopy (FTIR)
Fourier Transform-Infrared Spectroscopy (FTIR) is an analytical technique used to identify organic (and in some cases inorganic) materials. This technique measures the absorption of infrared radiation by the sample material versus wavelength. The infrared absorption bands identify molecular components and structures.
When a material is irradiated with infrared radiation, absorbed IR radiation usually excites molecules into a higher vibrational state. The wavelength of light absorbed by a particular molecule is a function of the energy difference between the at-rest and excited vibrational states. The wavelengths that are absorbed by the sample are characteristic of its molecular structure .
FTIR analysis became the main used technique when specific analytical topics have to be addressed, mainly when non-destructive analysis is needed. In this respect, according to our opinion, challenging analytical issues are raised in two important cases; the first one is that when historic (archaeological) or artistic materials have to be analyzed while the second issue came from the analysis of highly- specific biomaterials
The FTIR spectrometer uses an interferometer to modulate the wavelength from a broadband infrared source. A detector measures the intensity of transmitting or reflected light as a function of its wavelength. The signal obtained from the detector is an interferogram, which must be analyzed by a computer using Fourier transforms to obtain a single-beam infrared spectrum. The FTIR spectra are usually presented as plots of intensity versus wavenumber (in cm-1). Wavenumber is the reciprocal of the wavelength. The intensity can be plotted as the percentage of light transmittance or absorbance at each wavenumber
• Identification of foreign materials
• Identification of bulk material compounds
• Identification of constituents in multilayered materials
• Quantitation of silicone, esters, etc., as contamination of various materials