Where and when did the ozone depletion start?

Question

Where and when did the ozone depletion start?

Answer 1

In the early 1970s, researchers began to investigate the effects of various chemicals on the ozone layer, particularly CFCs, which contain chlorine. They also examined the potential impacts of other chlorine sources. Chlorine from swimming pools, industrial plants, sea salt, and volcanoes does not reach the stratosphere. Chlorine compounds from these sources readily combine with water and repeated measurements show that they rain out of the troposphere very quickly. In contrast, CFCs are very stable and do not dissolve in rain. Thus, there are no natural processes that remove the CFCs from the lower atmosphere. Over time, winds drive the CFCs into the stratosphere.

The CFCs are so stable that only exposure to strong UV radiation breaks them down. When that happens, the CFC molecule releases atomic chlorine. One chlorine atom can destroy over 100,000 ozone molecules. The net effect is to destroy ozone faster than it is naturally created.

It is caused by the release of chlorofluorocarbons (CFCs) and other ozone-depleting substances (ODS), which were used widely as refrigerants, insulating foams, and solvents. The discussion below focuses on CFCs, but is relevant to all ODS. Although CFCs are heavier than air, they are eventually carried into the stratosphere in a process that can take as long as 2 to 5 years.

When CFCs reach the stratosphere, the ultraviolet radiation from the sun causes them to break apart and release chlorine atoms, which react with ozone, starting chemical cycles of ozone destruction that deplete the ozone layer. One chlorine atom can break apart more than 100,000 ozone molecules.

Other chemicals that damage the ozone layer include methyl bromide (used as a pesticide) and halons (used in fire extinguishers). As methyl bromide and halons are broken apart, they release bromine atoms, which are 40 times more destructive to ozone molecules than chlorine atoms.

How do we know that natural sources are not responsible for ozone depletion?

While it is true that volcanoes and oceans release large amounts of chlorine, the chlorine from these sources is easily dissolved in water and washes out of the atmosphere in rain. In contrast, CFCs are not broken down in the lower atmosphere and do not dissolve in water. The chlorine in these human-made molecules does reach the stratosphere. Measurements show that the increase in stratospheric chlorine since 1985 matches the amount released from CFCs and other ozone-depleting substances produced and released by human activities.

What is being done about ozone depletion?

In 1978, the use of CFC propellants in spray cans was banned in the U.S. In the 1980s, the Antarctic “ozone hole” appeared and an international science assessment more strongly linked the release of CFCs and ozone depletion. It became evident that a stronger worldwide response was needed. In 1987, the Montreal Protocol was signed and the signatory nations committed themselves to a reduction in the use of CFCs and other ozone-depleting substances.

Since that time, the treaty has been amended to ban CFC production after 1995 in the developed countries, and later in developing. Today, over 160 countries have signed the treaty. Beginning January 1, 1996, only recycled and stockpiled CFCs will be available for use in developed countries like the US. This production phaseout is possible because of efforts to ensure that there will be substitute chemicals and technologies for all CFC uses.

Will the ozone layer recover? Can we make more ozone to fill in the hole?

The answers, in order, are: yes and no. We can't make enough ozone to replace what's been destroyed, but provided that we stop producing ozone-depleting substances, natural ozone production reactions should return the ozone layer to normal levels by about 2050. It is very important that the world comply with the Montreal Protocol; delays in ending production could result in additional damage and prolong the ozone layer's recovery.