One of today’s world's main challenges is access to a clean environment. The release of hazardous and toxic gases from burning fossil fuels is of critical concern due to these gases' destructive effects on the nearby atmosphere. Among these, acid rain is one of the most severe consequences of air pollution caused by sulfur dioxide (SO2) gas and still needs to be better addressed. One of the solutions is the adsorption-based technologies because of their ease of use, possible high adsorption capacity, minimum environmental impact, low cost, and efficient sorbate recovery possibilities. Gas separation via adsorption is not yet widely employed commercially since it needs regenerable, high-durable, high-performance, and cost-effective adsorbents. One of the common methods of absorbing acid gases is the use of amino absorbents that have disadvantages such as create many waste materials challenging to regenerate, wastewater, and waste gas. Therefore, incorporating amine groups on the surface of solids to overcome the problem of regeneration has attracted considerable attention in gas uptake. In this project, we proposed to functionalize nanocrystalline cellulose (NCC) using a solvent-free method to boost their SO2 interactions and thus their adsorption capability. Therefore, a commercial NCC material was modified using ethylenediamine (EDA) in green and straightforward amination approach in order to tune its surface basicity and obtain an efficient green-biobased adsorbent. Since the substitution process of amines with hydroxyl groups on the cellulose surface is carried out through dangerous halogen solvents, we used the solvent-free one-step method and investigated the synthetic parameters. Amination conditions of NCC adsorbents were optimized via the effects of the amination temperature, the amination time, and the amount of EDA on their physical properties and their performance for SO2 adsorption. The sorbents were characterized using attenuated total reflection-Fourier-transform infrared spectroscopy (ATR-FTIR), solid carbon nuclear magnetic resonance (13CNMR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and scanning electron microscopy- energy-dispersive X-ray spectroscopy (SEM-EDS) to see if EDA was incorporated into the NCC and investigate the changes in thermal stability of adsorbents by changing synthesis conditions. Sorbents were then tested for SO2 capture at the same conditions of room temperature (RT), atmospheric pressure, and a flow rate of 20 ml/min, which was selected based on previous studies to optimize flow rate in the same research group. The optimal conditions to create an effective sulfur dioxide adsorbent were found to be 70 oC for 8 hours of amination. At ideal conditions, the NCC modified had an SO2 adsorption capacity value of 0.030 mg/100 mg. The promising properties of EDA-NCC in terms of adsorption capacity (showing a significant increase in capacity when compared to the NCC at atmospheric pressure and ambient temperature) make them potential adsorbent candidates. In addition, the impacts of SO2 capture operating conditions on adsorption capacity were evaluated. By varying the adsorption temperature from room temperature to 60 °C and the feed flow rate from 10 to 30 ml min-1, fixed-bed breakthrough studies for SO2 adsorption onto NCC and modified-NCC adsorbent (prepared at 70oC, 3hr, and EDA/NCC=25) were carried out. Over the range of operating parameters studied, the greatest SO2 capacity and breakthrough time values were obtained with adsorbent at room temperature and 20 ml min-1 input flow rate. As expected, due to the exothermic nature of the adsorption process, the amount of SO2 adsorbed at equilibrium decreased with increasing temperature. It was also observed that as the flow rate increases, the breakthrough time decreases due to the higher flow rate of the feed gas was accompanied by the faster transport of the adsorbate molecules and leading to a shorter breakthrough time, as expected. Finally, another EDA functionalization method was tested, using a two-step method. First, cellulose was functionalized using citric acid (CA), and then the EDA was incorporated via carboxylic acid functional groups in the CA to obtain both amide and amine groups on the NCC’s surface. This approach aimed to compare EDA deposition on cellulose surface via a different method by adding one more functional group and evaluating their performance in SO2 gas adsorption. It was concluded that oxygenated functional groups and groups with low alkalinities, such as carboxylic acid and amide, can negatively affect gas adsorption. These results were concluded by comparing two adsorbents, one containing only amine groups and the other adsorbent containing amide and carboxylic acid groups in addition to the amine group, although the amine content of the two adsorbents was different. Future research will explore the mechanisms and capturing phenomena to improve capturing capacity and process applicability as well as the material optimal regeneration operating conditions.

No description available.