Friday, July 23, 2010

Removal of arsenic


Arsenic which exists in the form of arsenate or As(V), which are commonly found in aerobic surface waters are more easily removed compared to that of arsenite or As(III), which is common in anaerobic ground water. Hence, the removal technologies shown below are more effective in removing arsenate or As(V). The reason for this is due to the difference in charges of arsenate and arsenite, with arsenate being negatively charged and arsenite being neutral in charge.

If however, arsenite is predominant in the water sample, it can be oxidized into arsenate by pre-oxidation to arsenate. Some of the oxidizing agents that we can use include chlorine, ferric chloride, and potassium permanganate. Another alternative is by using ozone and hydrogen peroxide, but they might not be as effective as no data are available on performance.
Besides removing arsenic using the technologies mentioned below, there are three basic methods that we can prevent arsenic exposure:
1. treating arsenic contaminated groundwater
2. drawing water from uncontaminated acquifers.
3. using water from other sources such as rivers, rainfalls or ponds.
However, this may not be practical for certain regions which does not have the necessary technologies or sources, especially in poor countries like Bangladesh.


Current technologies for arsenic removal

Coagulation/Filtration (C/F) is an effective treatment process for the removal of arsenic. The efficiency of this process is affected by pH as the efficiency will be reduced when the pH becomes too high or too low. One main cause of concern is that the nearby landfills may not be willing to accept this arsenic-contaminated coagulation sludge for disposal. Hence, disposal of sludge may be a problem. Well trained operators may be required for this process. This process is also very costly and the process performance may vary.



Lime Softening (LS) provides a high efficiency for arsenic removal under certain conditions. It has to be conducted at a pH of greater than 10.5 provided that the influent concentration is 50 µg/L. However, in order to further reduce the concentration of the pollutant, it may require a secondary treatment process. The following diagram shows the process of lime softening.




















Activated Alumina(AA) is effective for treating water that has a high concentration of Total Suspended Solids(TDS). However, other elements such as selenium, fluoride, chloride, and sulphate, when present at high concentrations, may interfere with the removal process. This removal process is highly selective towards arsenic. One cause of concern that it may not be efficient in the long term, as it loses its adsorptive capacity with time. As this process releases highly concentrated waste streams, disposal may be a problem as well.



















Ion Exchange (IE) is effective for removing arsenic. However, sulfate, TDS, selenium, fluoride, and nitrate can also interfere with the removal process. Systems containing high levels of these constituents may require pretreatment. As this process produces highly concentrated waste by-product stream, disposal may be a problem as well. The following diagram shows the process of ion exchange.



Reverse Osmosis (RO) is able to remove as much as 95% of arsenic when the right amount of operating pressure is applied. This removal process may not be suitable to be used in water-scarce regions due to water rejection.(about 20-25% of influent).





Electrodialysis Reversal (EDR) is able to achieve a removal efficiency of 80%. Studies have shown that this process can reduce an influent concentration of 21 µg/L to only 3 µg/L, which shows a decrease in 19 µg/L of arsenic concentration. Similar to reverse osmosis, there is water rejection as well. Compared to RO, this process may not be cost competitive and as efficient. However, it is easier to operate. The following diagram shows a diagram of the EDR module.






Nanofiltration (NF) can achieve a removal efficiency of over 90%. However, this method of removal might not be suitable for regions where water is scarce as the water from the influent may be rejected by as much as 25%.








Recent breakthroughs of arsenic removal


Instead of using the conventional man-made techniques to remove arsenic as mentioned above, we can now use bacteria to remove arsenic. Scientists have recently discovered a new kind of microbe that posses the ability to use this poison to turn sunlight into food. In other words, it uses arsenic to power photosynthesis, which is a process whereby plants and bacteria convert sunlight into food. This bacteria is found in a hot spring in California as they have the ability to thrive in hot temperatures. However, the bacteria can only perform this removal in the presence of sunlight, which is a basic requirement for the process of photosynthesis.



The red slime mat shown in this picture is made up of the bacteria that uses arsenic to power photosynthesis.

Tuesday, July 20, 2010

What are the sources?

Natural sources of arsenic






Contaminated food [Seafoods]









Ground water used for drinking water supply












volcanic action










 








Low temperature volatilization













    Groundwater










    Man-made sources





    medications

    • ore smelting/refining/processing plants, galvanizing, etching and plating processes

    burning of fossil fuels especially in coal-fired power generation plants

    Tailings from or river bottoms near gold mining areas (past or present)

    Agricultural chemicals: Insecticides, rodenticides and fungicides

    Commercial arsenic products which include: sodium arsenite, calcium arsenate, and lead arsenate.

    • "Paris green" (cupric acetoarsenite) a wood preservative.

    Burning of vegetation



    Ore smelting at an industry





    A global phenomena



    Bangladesh is not the only country with arsenic pollution of the groundwater, but pollution is exceptionally widespread around the world.



    Many other countries and districts in South East Asia, such as Vietnam, Cambodia, and China have geological environments conducive to generation of high-arsenic groundwater.











    Footage of people suffering due to arsenic poisoning in bangledesh

    Thursday, July 15, 2010

    Portable X-ray Fluorescence






    X-ray fluorescence (XRF) is the emission of characteristic "secondary" (or fluorescent) X-rays from a material that has been excited by bombarding with high-energy X-rays or gamma rays. Besides measuring arsenic, it can be used to analyse other elements and chemicals like the investigation of metals, glass, ceramics, and building materials and for research in geochemistry, forensic science and archaeology. The following diagram shows the basic working principle of this process.








    The amount of photon emitted will help us determine the concentration of the arsenic in the sample. A photon is a  discrete bundle of light energy.

    Portable X-ray fluorescence is used to measure arsenic in dry solid samples, such as soil and dried sludge. The main interferents listed in this method were variations in particle size, moisture, and lead co-contamination.


    Advantages:


    -Measuring devices are normally portable

    - It can directly measure arsenic in the soil without having to extract the soil from the ground.

    - Can measure a wide variety of metals besides arsenic

    - Flexible as it can be used for measuring arsenic in both liquid and solid samples.


    Disadvantages:

    -It is not suitable for the detection of low concentrations of arsenic especially in drinking water as detection is only accurate at gram per litre concentrations.

    -results can be interfered when lead is present in the sample

    -many models contain a radioactive source, which may cause health effects to the user if not properly handled. However, research efforts have proven that this radioactive source can be eliminated and replaced by a less harmful source.

    The Wagtech Arsenator system

    A quick and portable device available in the market to detect concentration of arsenic.





    The complete system comes with sufficient reagents and consumables for over 400 tests. The following are the advantages of using the Arsenator:

    Low cost digital arsenic testing device

    Fully portable, designed specially for field use

    Immediate results in the field in less than 20 minutes

    Simple, safe and easy to operate

    Gives accurate test results between the critical range of 2µgl (ppb) to 100µgl (ppb)

    • Designed in conjunction with Prof. Walter Kosmus and laboratory tested by Imperial College London

    • Field tested in conjunction with UNICEF/WHO WAT/SAN monitoring programmes

    Environmentally friendly

    Colorimetric Test Kits


    Detection using field test kits are very common and are used extensively to monitor arsenic in groundwater. This method of detection is based on the "Gutzeit" method which is developed over 100 years ago. Besides using it for detection in water samples, it can also be applied to testing solid waste and soil by acid extraction or acidic oxidation digestion of the sample.



    The following illustrates the procedures of the “Gutzeit” method :

    1. treat the water sample with a reducing agent that transforms the arsenic compounds present in the water into arsenic trihydride (arsine gas).

    2. Arsenic is separated from the sample

    3. The arsenic trihydride diffuses out of the sample where it is exposed to a paper impregnated with mercuric bromide.


    AsH3 + 3HgBr2 → As(HgBr)3 + 3HBr

    The white mercury(II) bromide will turn yellow, brown, or black if arsenic is present in the sample


    4. The reaction with the paper produces a highly colored compound.

    5. The concentration of the arsenic can be approximated using a calibrated color scale.



    This method of detection has several pros and cons as shown below.


    Advantages:

    • inexpensive
    • minimally trained personnel can readily perform it and read the results in the field.

    Disadvantage:

    • sulfur, selenium, and tellurium compounds have the potential of interfering with this assay.