How to Reactivate Activated Carbon

Activated carbon (AC) is a highly porous material prized across numerous industries for its exceptional ability to remove contaminants from liquids and gases through adsorption. This material offers an immense internal surface area, often equivalent to over a hundred acres per pound, where purification takes place. However, this capacity is finite, and the AC eventually becomes saturated, or “spent,” requiring replacement or treatment. Reactivating spent carbon is a necessary practice driven by both economics and environmental stewardship. Since producing virgin AC is costly and energy-intensive, restoring the material’s function reduces the need for new resources, lowers waste volume, and aligns with circular economy goals.

Understanding Carbon Saturation and Deactivation

Activated carbon stops functioning effectively when its internal pore structure becomes blocked by adsorbed substances, known as adsorbates. This saturation diminishes the available surface area necessary for continued purification. The mechanism of attachment often involves physical adsorption, where contaminants are loosely held to the carbon surface by weak intermolecular forces like Van der Waal’s forces, a process which is generally reversible. However, some contaminants bind through chemisorption, forming stronger chemical bonds at the carbon interface, which is less easily reversed. As the pores fill, the overall capacity of the carbon bed decreases, and contaminants eventually begin to “break through” the filter. The trapped material must be removed to restore the internal structure of the pores for the carbon to be reused.

Industrial Thermal Reactivation Processes

The dominant and most comprehensive technique for restoring spent activated carbon is industrial thermal reactivation, which uses extreme heat in a controlled environment. This process is typically conducted in specialized equipment, such as rotary kilns or multiple hearth furnaces, and involves three distinct stages designed to systematically strip and destroy the contaminants.

Drying

The first stage is drying, where the spent carbon is heated to a temperature between 100°C and 150°C to remove physical moisture and volatile components. This initial step prevents steam explosions and thermal shock when the carbon is subjected to much higher temperatures.

Pyrolysis

Following drying, the carbon moves into the pyrolysis stage, sometimes called high-temperature carbonization. Here, the temperature is raised significantly, often ranging from 500°C to 800°C, in an inert atmosphere, usually containing nitrogen or flue gas, to prevent the carbon itself from oxidizing. During pyrolysis, the organic contaminants boil, vaporize, and decompose into smaller hydrocarbon molecules. Non-volatile residuals are converted into a carbonized char that remains lodged in the pores.

Gasification

The final stage is the gasification or activation phase, which restores the original pore structure. The temperature is further elevated to a range of 800°C to 950°C. A controlled amount of an oxidizing agent, typically low-pressure steam or carbon dioxide, is introduced. This agent selectively reacts with the residual carbonized char left in the pores, converting it into gases like carbon monoxide and hydrogen. This selective gasification cleans out the internal channels, reopening the micro- and mesopores to return the material to a high state of adsorption capacity.

Alternative and Small-Scale Reactivation Methods

While thermal processing is the industry standard, other methods exist that may be suitable for specific contaminants or smaller-scale operations.

Chemical reactivation uses solvents, acids, or bases to target and dissolve particular adsorbed substances. An acid wash with hydrochloric or sulfuric acid can be effective at removing inorganic contaminants like precipitated metals. However, this method is highly contaminant-specific and generally less effective at comprehensive pore restoration than high-temperature thermal treatment.

Microwave reactivation is a promising alternative that uses electromagnetic energy to rapidly and uniformly heat the carbon, sometimes coupled with an inert gas or steam. This method focuses energy directly on the material, which can result in faster processing times and potentially lower energy consumption compared to traditional external heating.

Another approach is the wet air oxidation method, which uses moderate temperatures (around 230°C) and high pressure in a liquid phase with oxygen or air to oxidize and decompose organic adsorbates. Simple, low-tech methods, such as hot water rinsing or low-temperature baking, offer only minimal pore restoration, as they only remove loosely bound or highly volatile compounds and do not address stubborn, carbonized residues.

Assessing Performance and Reactivation Limits

The success of any reactivation process is measured by how closely the restored material’s performance matches that of virgin carbon. Industry professionals rely on standardized performance metrics.

The Iodine Number quantifies the material’s ability to adsorb iodine from a solution, providing an indicator of the micropore surface area. Another common metric is the Butane working capacity, which measures the carbon’s capacity for adsorbing a volatile organic compound in the vapor phase. Ideally, reactivated carbon should retain 80% to 95% of its original adsorption capacity to be considered viable for reuse.

A significant limitation of the thermal method is the inevitable mass loss that occurs with each cycle, typically ranging from 5% to 15% of the carbon’s weight. This loss is due to the physical degradation of the granules and the burning off of the carbonized char during the high-temperature gasification stage. Repeated cycles weaken the physical granules, limiting the material’s overall lifespan and necessitating the addition of new carbon to maintain volume. The decision to reactivate is ultimately an economic one, balancing the cost of energy and handling against the higher procurement cost of virgin activated carbon.