Effective degradation of tetracycline in aqueous solution by an electro-Fenton process using chemically modified carbon/α-FeOOH as catalyst.

This study applied an electro-Fenton process using chemically modified activated carbon derived from rubber seed shells loaded with α-FeOOH (RSCF) as catalyst to remove tetracycline residues from aquatic environment. Catalyst characteristics were evaluated using SEM, EDS, XRD, and XPS, showing successful insertion of iron onto the activated carbon. The effects of the parameters were investigated, and the highest treatment efficiency was achieved at pH of 3, Fe: H2O2 ratio (w/w) of 500:1, catalyst dose of 1 g/L, initial TCH concentration of 100 mg/L, and electric current of 150 mA, with more than 90% of TCH being eliminated within 30 min. Furthermore, even after five cycles of use, the treatment efficiency remains above 90%. The rate constant is calculated to be 0.218 min-1, with high regression coefficients (R 2 = 0.93). The activation energy (Ea) was found to be 32.2 kJ/mol, indicating that the degradation of TCH was a simple reaction with a low activation energy. These findings showed that the RSCF is a highly efficient and cost-effective catalyst for TCH degradation. Moreover, the use of e-Fenton process has the advantage of high efficiency, low cost thanks to the recyclability of the catalyst, and environmental friendliness thanks to less use of H2O2.

Enhanced adsorption of aqueous chlorinated aromatic compounds by nitrogen auto-doped biochar produced through pyrolysis of rubber-seed shell.

The adsorption of chlorinated aromatic compounds (CACs) on pristine biochar was often limited. Surface modification can greatly improve the adsorption capacity of biochar. In this work, by pyrolysis activation of rubber-seed shell wastes, nitrogen auto-doped biochar (RSS-NBC) was synthesized and used for purifying CACs-containing wastewater. Systematic characterization results showed that after proper treatment, the as-prepared RSS-NBC had high specific surface area, abundant surface oxygen- and nitrogen-containing functional groups, and nano-scale pore structure. Batch adsorption experiments were conducted with using three typical CACs probing pollutants, i.e. 1,2-dichlorobenzene (1,2-DCB), 2,4-dichlorophenol (2,4-DCP) and 2,4-dichlorobenzoic acid (2,4-DCBA). The adsorption experiments results showed that the maximum adsorption amounts of 1, 2-DCB, 2,4-DCP, and 2,4-DCBA could reach 2284, 1921, and 1142 mg/g at 298.15 K. Moreover, 90% of the equilibrium adsorption amount can be reached within 0.5 h. The adsorption kinetic results showed that the adsorption processes of the three CACs followed the pseudo-second-order rate model and were dominated by chemisorption. Also, the adsorption isotherms of 1, 2-DCB and 2, 4-DCP belonged to the Freundlich model and were valid for multilayer adsorption, while the adsorption of 2,4-DCBA followed Langmuir model and single-layer adsorption. The thermodynamics data indicated that the spontaneous adsorption process of 1, 2-DCB and 2, 4-DCP was endothermic while that of 2,4-DCBA was exothermic. After 5 cycles of adsorption-regeneration, the removal efficiency of RSS-NBC particles still remained more than 80% for the three typical CACs, indicating that it could be reused as an effective and retrievable adsorbent in the treatment of CACs-containing effluents.

One-Pot Synthesis of Rubber Seed Shell-Derived N-Doped Ultramicroporous Carbons for Efficient CO2 Adsorption.

In this work, a series of novel rubber seed shell-derived N-doped ultramicroporous carbons (NPCs) were prepared by one-step high-temperature activation (500-1000 °C), using melamine as the nitrogen source and KOH as the activator. The effects of the melamine dosage and the activation temperatures on the surface chemical properties (doped N contents and N species), textural properties (surface area, pore structure, and microporosity), CO2 adsorption capacities, and CO2/N2 selectivity were thoroughly investigated and characterized. These as-prepared NPCs demonstrate controllable BET surface areas (398-2163 m2/g), ultramicroporosity, and doped nitrogen contents (0.82-7.52 wt%). It was found that the ultramicroporosity and the doped nitrogens significantly affected the CO2 adsorption and the separation performance at low pressure. Among the NPCs, highly microporous NPC-600-4 demonstrates the largest CO2 adsorption capacity of 5.81 mmol/g (273 K, 1.0 bar) and 3.82 mmol/g (298 K, 1.0 bar), as well as a high CO2/N2 selectivity of 36.6, surpassing a lot of reported biomass-based porous carbons. In addition, NPC-600-4 also shows excellent thermal stability and recycle performance, indicating the competitive application potential in practical CO2 capture. This work also presents a facile one-pot synthesis method to prepare high-performance biomass-based NPCs.

Adsorption of uremic toxins using biochar for dialysate regeneration.

Numerous studies have shown that patients with COVID-19 have a high incidence of renal dysfunction. However, the dialysis supplies, including dialysates, are also severely inadequate in hospitals at the pandemic centers. Therefore, there is an urgent need to develop materials that can efficiently and rapidly remove toxins and thus regenerate dialysate to make this vital resource remains readily available. In this work, by simple carbonization and activation treatment, the porous activated carbon from waste rubber seed shell (RAC) was prepared. The adsorption results showed that the maximum adsorption capacities of the obtained RAC for creatinine and uric acid were 430 mg/g and 504 mg/g, respectively. Significantly, the adsorption process can be close to the equilibrium state within 0.5 h, which proved the ultra-fast adsorption response capacity of RAC. Further, the thermodynamics analysis results showed that both the creatinine and uric acid adsorption processes were monolayer, exothermic, and spontaneous. The adsorption kinetics results indicated that the adsorption process of the two uremic toxins followed the pseudo-second-order rate model and was dominated by chemisorption. The instrument analysis results reflected the efficient adsorption of the RAC for the above uremic toxins which might be due to the dipole-dipole interaction between the dipolar oxygen-containing groups of the surface of RAC and the dipoles of the toxins. Moreover, the formed hydrogen bonds between the oxygen groups and the toxins also played an important role. In all, the as-prepared RAC has the potential to efficiently remove major toxins from the dialysate and can be used in in vitro dialysis of numerous patients during the current COVID-19 pandemic.

Activation of Rubber-Seed Shell Waste by Malic Acid as Potential CO2 Removal: Isotherm and Kinetics Studies.

Carbon dioxide (CO2) has been deemed a significant contributor to the climate crisis and has an impact on environmental systems. Adsorption is widely used among other technologies for carbon capture because of its many benefits. As a starting material for the production of activated carbon (AC) by chemical activation using malic acid due to its biodegradable and non-toxic properties, rubber seed shell (RSS) was used as agricultural waste from rubber farming. Sample A6, which was carbonized for 120 min at a temperature of 600 °C and impregnated at a ratio of 1:2, was identified to achieve the highest surface area of 938.61 m2/g with micropore diameter of 1.368 nm, respectively. Using the fixed volumetric approach measured at 25, 50, and 100 °C, the maximum CO2 adsorption capability reported is 59.73 cm3/g of adsorbent. Using the pseudo-first order of Lagergren, the pseudo-second order and the Elovich model, experimental data is modeled. It appears that, based on the correlation coefficient, the pseudo-first order model is aligned with the experimental findings. Furthermore, the activation energy of under 40 kJ/mol indicated a physical adsorption occurs, indicating that the RSS chemically activated with malic acid is a fascinating source of CO2 removal requirements.