The chemistry of lead in drinking water

Our county, like many in the US and Canada, is served by thousands of miles of lead pipes. Some of these are the property of the government, others sit beneath our homes and are the property of the home-owner. These pipes are usually safe, but sometimes poison us. There is also problem of lead-tin solder. It was used universally to connect iron and copper pipes until it was outlawed in 1986. After years of sitting quietly, this lead caused a poisoning crisis in DC in 2004, and in Flint in 2015-16. Last month my town, Oak Park, registered dangerous lead levels in the drinking water. In an attempt to help, please find the following summary of the relevant lead chemistry. Maybe people in my town, or in other towns, will find some clue here to what’s going on, and what they can do to fix it.

lead pipes showing the three oxides: brown, yellow, and red, PbO2, PbO, and Pb2O3.

Left to itself, lead and solder pipe could be safe; lead is not soluble in clean water. But, if the water becomes corrosive, as happens every now and again, the lead becomes oxidized to one of several compounds that are soluble. These oxides are the main route of poisoning; they can present serious health issues including slow development, joint and muscle pain, memory issues, vomiting, and death. The legal limit for lead content in US drinking water is 15 ppb, a level that is far below that associated with any of the above. The solubility of PbO, lead II oxide, is more than 1000 times this limit 0.017 g/L, or 17,000 ppb. At this concentration serious health issues will show up.

PbO is the yellow lead oxide shown in the center of the figure above, right; the other pipes show other oxides, that are less-soluble, and thus less dangerous. Yellow lead oxide and red lead oxides on the right were used as paint colors until well into the 20th century. Red lead oxide is fairly neutral, but yellow PbO is a base; its solubility is strongly dependent on the PH of the water. In neutral water, its solution can be described by the following reaction.

PbO + H2O(l) –> Pb2+(aq) + 2 OH(aq).

In high pH water (basic water), there are many OH(aq) ions, and the solubility is lower. In low pH, acidic water the solubility is even higher. For every 1 point of lower pH the lowubility increases by a factor of 10, for every 1 point of higher pH, it decreases by a factor of ten. In most of our county, the water is slightly basic, about pH 8. It also helps that our water contains carbonate. Yellow lead forms basic lead carbonate, 2PbCO3·Pb(OH)2, the white lead that was used in paint and cosmetics. Its solubliity is lower than that of PbO, 110 ppb, in pure water, or within legal limit in water of pH 8. If you eat white lead, though, it reacts with stomach acid, pH 2, and becomes quite soluble and deadly. Remember, each number here is a factor of ten.

A main reason lead levels a very low today are essentially zero, even in homes with lead solder or pipe, involves involves the interaction with hypochlorite. Most water systems add hypochlorite to kill bacteria (germs) in the water. A side benefit is significant removal of lead ion, Pb2+(aq).

Pb2+(aq) + 2 ClO(aq) –> Pb(ClO)2(s). 

Any dissolved lead reacts with some hypochlorite ion reacts to form insoluble lead hypochlorite. Lead hypochlorite can slowly convert to Lead IV oxide — the brown pyrophilic form of lead shown on the left pipe in the figure above. This oxide is insoluble. Alkaline waters favor this reaction, decreasing solubility, but unlike with PbO, highly alkaline waters provide no significant advantage.

PbClO+(aq) + H2O(l) –> PbO2(s) + 2 H+(aq) + Cl(aq)

Lead IV oxide, PbO2 was used in old-fashioned matches; it reacts violently with phosphorus or sulfur. People were sometimes poisoned by sucking on these matches. In the stomach, or the presence of acidic drinking water, PbO2 is decomposed forming soluble PbO:

PbO2(s) +2 H+(aq) + 2 e –> PbO(s) + H2O(l).

You may wonder at the presence of the two electrons in the reaction above. A common source in water systems is the oxidation of sulphite:

SO3-2(aq)–> SO4-2(aq) + 2 e.

The presence of sulphite in the water means that hypochlorite is removed.

ClO(aq) + 2 H+(aq) + 2 e —> Cl(aq) + H2O(l).

Removal of hypochlorite can present a serious danger, in part because the PbO2(s) slowly reverts to PbO and becomes soluble, but mostly because bacteria start multiplying. In the Flint crisis of 2016, and in a previous crisis in Washington DC, the main problem, in my opinion was a lack of hypochlorite addition. The lead crisis was preceded by an uptick in legionnaires disease; It killed 12 people in Flint in 2014 and 2015, and 87 were sickened, all before the lead crisis. Eventually, it was the rise of legionaries disease that alerted water officials in Virginia that there was something seriously wrong in Flint. Most folks were unaware because Flint water inspectors seem to have been fudging the lead numbers to make things look better.

Most US systems add phosphate to remove lead from the water. Flint water folks could have stopped the lead crisis, but not the legionnaires, by adding more phosphate. Lead phosphate solubility is 14 ppb at 20°C, and my suspicion is that this is the reason that the legal limit in the US is 15 ppb. Regulators chose 15 ppb, I suspect, not for health reasons, but because the target could be met easily through the addition of phosphate. Some water systems in the US and Canada disinfect with chloramine, not hypochlorite, and these systems rely entirely on phosphate to keep lead levels down. Excess phosphate is used in Canada to lower lead levels below 10 ppb. It works better on systems with hypochlorite.

Chloramine is formed by reacting hypochlorite with ammonia. It may be safer than hypochlorite in terms of chlorite reaction products, a real problem when the water source is polluted. But chloramine is not safe. It sickened 72 soldiers, 36 male and 36 female in 1998. They’d used ammonia and bleach for a “cleaning party” on successive days. Here’s a report and first aid instructions for the poisoning. That switching to chloramine can expose people to lead is called “the chloramine catch”.

Unlike PbO, PbO2 is a weak acid. PbO2 and PbO can react to form red lead, PbO•PbO2(s), the red stuff on the pipe at right in the picture above. Red lead can react with rust to form iron plumbable, an insoluble corrosion resister. A simple version is:

PbO•PbO2(s) + Fe2O3(s) —> 2FePbO3(s).

This reaction is the basis of red-lead, anti-rust compounds. Iron plumbable is considered to be completely insoluble in water, but like PbO it is soluble in acid. Bottom line, slightly basic water is good, as are hypochlorite in moderation, and phosphate.

Robert Buxbaum, November 18, 2019. I ran for water commissioner, and might run again. Even without being water commissioner, I’ll be happy to lend my expertise, for free, to any Michigan town or county that is not too far from my home.

2 thoughts on “The chemistry of lead in drinking water

  1. Pingback: The main route of lead poisoning is from the soil by way of food, dust, and smoke. | REB Research Blog

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