sample preparation for inorganic trace analysis lecture 2

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AHMAD RAZALI BIN ISHAK DEPARTMENT OF ENVIRONMENTAL HEALTH FACULTY OF HEALTH SCIENCES UITM PUNCAK ALAM Sample Preparation for inorganic trace analysis Lecture 2

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Sample Preparation for inorganic trace analysis Lecture 2. Ahmad Razali Bin Ishak Department of Environmental Health Faculty of Health Sciences UiTM Puncak Alam. Solid Samples. Introduction. Analysis for metals in solids-2 different approach - PowerPoint PPT Presentation

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Page 1: Sample Preparation for inorganic trace analysis Lecture 2

AHMAD RAZALI BIN ISHAKDEPARTMENT OF ENVIRONMENTAL HEALTHFACULTY OF HEALTH SCIENCESUITM PUNCAK ALAM

Sample Preparation for inorganic trace analysis

Lecture 2

Page 2: Sample Preparation for inorganic trace analysis Lecture 2

Solid Samples

Page 3: Sample Preparation for inorganic trace analysis Lecture 2

Introduction

Analysis for metals in solids-2 different approach

1. Direct analysis of solid-X-ray florescence (self study-assignment)

2. After decomposition

Page 4: Sample Preparation for inorganic trace analysis Lecture 2

Decomposition techniques

involves liberation of analyte (metal) of interest from interfering matrix

Using a reagent (mineral/oxidizing acids or fusion or flux) And/or Heat

Problem- risk of contamination and loss of analytes

Page 5: Sample Preparation for inorganic trace analysis Lecture 2

Dry ashing

The simplest of all decomposition systems involves the heating of the samples in porcelain crucible in a muffle furnace in the presence of air at 400-800C

After decomposition, the residue is dissolved in acid and transferred to a volumetric flask prior to analysis.

Allow organic matter to be destroyed.May lead to the loss of volatile elements (Hg,

Cd, Ca, As, Sb, Cr and Cu)

Page 6: Sample Preparation for inorganic trace analysis Lecture 2

Cont..

Disadvantages of this method: Loss due to volatilization Resistance to ashing by some materials Difficult dissolution of ashed materials High risk of contamination

It has largely been replace by wet ashing

Page 7: Sample Preparation for inorganic trace analysis Lecture 2

Wet digestion (Acid digestion)

The use of mineral or oxidizing acids and an external heat sources to decompose the sample matrix.

The choice of an individual acids is dependent upon the nature of the matrix to be decomposed

Page 8: Sample Preparation for inorganic trace analysis Lecture 2

Once the choice of acid is made the sample is placed into an appropriate vessel for decomposition stage

Vessel- carried out in open glass vessels(beakers or boiling tubes) using hotplate (in FSK) or multiple sample digester

The US EPA method for acid digestion of sediments, sludges and soils are outlined in figure 1

Page 9: Sample Preparation for inorganic trace analysis Lecture 2

Figure 1

Page 10: Sample Preparation for inorganic trace analysis Lecture 2

The digestion of food stuffs can be carried out in a similar manner

A typical procedure for digestion of foodstuffs e.g. cereals, meats, fish and vegetable for determination of total metal content (cadmium,cooper,iron, lead and zinc) in figure 2

Page 11: Sample Preparation for inorganic trace analysis Lecture 2

Figure 2

Page 12: Sample Preparation for inorganic trace analysis Lecture 2

Microwave digestion

An alternative approach to conventional heating involves the use of microwave heating

Advances in technology by a variety of manufacturers means that today there are two types of microwave heating systems commercially available : open-focused and closed vessel system.

Page 13: Sample Preparation for inorganic trace analysis Lecture 2

closed vessel system

Page 14: Sample Preparation for inorganic trace analysis Lecture 2

Liquids-Natural and waste waters

Page 15: Sample Preparation for inorganic trace analysis Lecture 2

Introduction

Analysis of liquid samples for metals-required no sample pre-treatment-just a simple filtration (0.2 um)of the sample to remove particulates prior to introduction into chosen instrument.

However, reality is often very different and even most sensitive of analytical technique (e.g. ICP-MS) may require some additional sample pre-treatment; separation or pre-concentration

Pretreatment/pre-concentration-potential contamination-great care required

Page 16: Sample Preparation for inorganic trace analysis Lecture 2

Liquid-liquid extraction

Addition of a suitable chelating agent to the water samples to form metal complex

Will effectively partition into an immiscible organic solvent

Metal present in a large volume of sample water is effectively and quantitatively transferred into a small volume of organic solvent.

Page 17: Sample Preparation for inorganic trace analysis Lecture 2

The important variables in LLE are as follows:

a) Choice of chelating agentb) Choice of organic solventc) pH of the aqueous sampleThe most commonly used chelating agent in

AAS is Ammonium pyrrolidine dithiocarbamate (APDC). This reagent can be directly extracted with methyl isobutyl ketone (MIBK) as the organic solvent.

Page 18: Sample Preparation for inorganic trace analysis Lecture 2

Typical procedure LLE of metals

Page 19: Sample Preparation for inorganic trace analysis Lecture 2

AHMAD RAZALI BIN ISHAKDEPARTMENT OF ENVIRONMENTAL HEALTHFACULTY OF HEALTH SCIENCESUITM PUNCAK ALAM

Sample preparation for organic analysis

Lecture 3

Page 20: Sample Preparation for inorganic trace analysis Lecture 2

Solid Samples

Page 21: Sample Preparation for inorganic trace analysis Lecture 2

Introduction

New instrumental approaches-led to development -speed of extraction, reduction in organic solvent consumption and introduction of automation.

However, this instrumental approaches-higher price tag than the conventional.

Extraction of env. Pollutant from solid or semi solid matrices can be divided into several categories based on the method of extraction, mode of heating, and presence or not of some type of agitation.

Page 22: Sample Preparation for inorganic trace analysis Lecture 2

Various method of extraction of analyte from solid matrices

Page 23: Sample Preparation for inorganic trace analysis Lecture 2

Types of extraction-Solid

Soxhlet extractionShake flask extractionUltrasonic extractionSupercritical Fluid Extraction (SFE)Microwave assisted extractionPressurized Fluid ExtractionMatrix solid phase dispersion

Page 24: Sample Preparation for inorganic trace analysis Lecture 2

Soxhlet Extraction

The basis of soxhlet extraction apparatus consist of a solvent reservoir, and extraction body, a heat sources (e.g. isomantle) and a water-cooled reflux condenser

A soxhlet uses a range of organic solvent to remove organic compounds, primarily from solid matrices

The solid sample (e.g. 10 g soil) and a similar mass of anhydrous sodium sulfate are placed in the porous thimble (cellulose) which in turn is located in the inner tube of Soxhlet apparatus

Page 25: Sample Preparation for inorganic trace analysis Lecture 2
Page 26: Sample Preparation for inorganic trace analysis Lecture 2

The apparatus is then fitted to a round- bottom flask of appropriate volume containing organic solvent of choice and to reflux condenser.

The solvent is then boiled gently-The solvent vapor passes up through the tube is condensed by the reflux condenser and the condensed solvent falls into the thimble and slowly fills the body of soxhlet apparatus

Page 27: Sample Preparation for inorganic trace analysis Lecture 2

When the solvent reaches the top of the tube, it syphons over into the round-bottomed flask the organic solvent containing the analyte extracted from the sample in the thimble. This solvent is then said to have completed one cycle.

The whole process is repeated frequently until the pre-set extraction time is reached.

Page 28: Sample Preparation for inorganic trace analysis Lecture 2

As the extracted analyte will normally have higher boiling point than the solvent, it is preferentially retained in the flask and fresh solvent re-circulates

Page 29: Sample Preparation for inorganic trace analysis Lecture 2

Typical procedure for Soxhlet extraction

Page 30: Sample Preparation for inorganic trace analysis Lecture 2

Shake Flask Extraction

Conventional LLE in the form of shake flask extraction is carried out by placing samples (e.g. soil) into a suitable glass container, adding a suitable organic solvent and the agitating or shaking

Page 31: Sample Preparation for inorganic trace analysis Lecture 2

Typical procedure used for shake flask extraction

Page 32: Sample Preparation for inorganic trace analysis Lecture 2

Ultrasonic extraction

Sonication involves the use of sound waves to agitate a sample immersed in an organic solvent-using sonic probe or sonic bath

The sample is placed in suitable glass container and enough organic solvent is then added to cover the sample.

The system is then sonicated for a short period typically 3 min using sonic bath or probe

After extraction, the solvent containing the analyte is separated by centrifugation and/or filtration and fresh solvent added.

The whole process is repeated three times and all of the solvent extract are then combined.

Page 33: Sample Preparation for inorganic trace analysis Lecture 2

Typical procedure for ultrasonic extraction

Page 34: Sample Preparation for inorganic trace analysis Lecture 2

Cont..

Page 35: Sample Preparation for inorganic trace analysis Lecture 2

Liquid Samples

Page 36: Sample Preparation for inorganic trace analysis Lecture 2

Types of extraction-Liquid

Liquid Liquid extraction (LLE)Solid phase extraction (SPE)Solid Phase Microextraction (SPME)

Page 37: Sample Preparation for inorganic trace analysis Lecture 2

Liquid-Liquid Extraction

The sample is distributed/partitioned into two immiscible solvent which analyte and matrix have different solubility

Advantage-wide availability of pure solvent, low cost apparatus

Page 38: Sample Preparation for inorganic trace analysis Lecture 2
Page 39: Sample Preparation for inorganic trace analysis Lecture 2

Typical procedure for LLE

Page 40: Sample Preparation for inorganic trace analysis Lecture 2

Solid phase extraction

Liquid-solid extractionBringing a liquid sample into contact with a

solid sorbent whereby the analyte is selectively adsorbed onto the surface of solid phase.

The latter is then separated from solution and other solvents are added.

Page 41: Sample Preparation for inorganic trace analysis Lecture 2

Solid Phase extraction

The first solvent-wash to remove possible contaminant

Then, Liquid sample bring into contact with a solid phase/sorbent whereby analyte is selectively adsorbed onto the surface of solid phase.

The analyte then separated from the solid phase by eluting solvent.

This solvent is then collected for analysis.

Page 42: Sample Preparation for inorganic trace analysis Lecture 2
Page 43: Sample Preparation for inorganic trace analysis Lecture 2

Typical procedure for SPE

Page 44: Sample Preparation for inorganic trace analysis Lecture 2

Solid Phase Micro Extraction (SPME)

The process whereby an analyte is adsorbed onto the surface of a coated silica fiber as a method of concentration.

This is follow by desorption of the analyte into a suitable instrument for separation and quantification

Page 45: Sample Preparation for inorganic trace analysis Lecture 2
Page 46: Sample Preparation for inorganic trace analysis Lecture 2

Volatile Compounds

Page 47: Sample Preparation for inorganic trace analysis Lecture 2

Introduction

Volatile compounds in the atmosphere, workplace and on industrial sites need to be monitored with regard to safety consideration

This VOC, can be trapped either on a solid support material (for thermal desorption) or liberated from water sample and then trapped (e.g. via purge and trap) prior to analysis.

Page 48: Sample Preparation for inorganic trace analysis Lecture 2

Self study

Thermal desorptionPurge-and-trap

Page 49: Sample Preparation for inorganic trace analysis Lecture 2

Thank You