This paper provides a comprehensive review of 71 previous studies on the life cycle assessment (LCA) of nanomaterials (NMs) from 2001 to 2020 (19 years). Although various studies have been carried out to assess the efficiency and potential of wastes for nanotechnology, little attention has been paid to conducting a comprehensive analysis related to the environmental performance and hotspot of NMs, based on LCA methodology. Therefore, this paper highlights and discusses LCA methodology's basis (goal and scope definition, system boundary, life cycle inventory, life cycle impact assessment, and interpretation) to insights into current practices, limitations, progress, and challenges of LCA application NMs. We found that there is still a lack of comprehensive LCA study on the environmental impacts of NMs until end-of-life stages, thereby potentially supporting misleading conclusions, in most of the previous studies reviewed. For a comprehensive evaluation of LCA of NMs, we recommend that future studies should: (1) report more detailed and transparent LCI data within NMs LCA studies; (2) consider the environmental impacts and potential risks of NMs within their whole life cycle; (3) adopt a transparent and prudent characterization model; and (4) include toxicity, uncertainty, and sensitivity assessments to analyze the exposure pathways of NMs further. Future recommendations towards improvement and harmonization of methodological for future research directions were discussed and provided. This study's findings redound to future research in the field of LCA NMs specifically, considering that the release of NMs into the environment is yet to be explored due to limited understanding of the mechanisms and pathways involved.
The potentials of biomass-based carbon quantum dot (CQD) as an adsorbent for batch adsorption of dyes and its photocatalytic degradation capacity for dyes which are congo red (CR) and methylene blue (MB) have been conducted in this study. The CQDs properties, performance, behaviour, and photoluminescence characteristics were assessed using batch adsorption experiments which were carried out under operating conditions including, temperature, pH and dosage. The morphological analysis revealed that CQDs are highly porous, uniform, closely aligned and multi-layered. The presence of hydroxyl, carboxyl and carbonyl functional groups indicated the significance of the oxygenated functional groups. Spectral analysis of photoluminescence for CQDs confirmed their photoluminescent quality by exhibiting high excitation intensity and possessing greenish-blue fluorescence under UV radiation. The removal percentage of the dyes adsorbed for both CR and MB dyes was 77% and 75%. Langmuir isotherm and pseudo-second-order models closely fitted the adsorption results. Thermodynamics analysis indicated that the adsorption process was exothermic and spontaneous, with excellent reusability and stability. The degradation efficiency of CQDs on both dyes was more than 90% under sunlight irradiation and obeyed the first-order kinetic model. These results demonstrated CQDs to be an excellent adsorbent and outstanding photocatalyst for organic dye degradation.
In this study, two biomass-based adsorbents were used as new precursors for optimizing synthesis conditions of a cost-effective powdered activated carbon (PAC). The PAC removed dyes from an aqueous solution using carbonization and activation by KOH, NaOH, and H2SO4. The optimum synthesis, activation temperature, time and impregnation ratio, removal rate, and uptake capacity were determined. The optimum PAC was analyzed and characterized using Fourier-transform infrared spectroscopy (FTIR), x-ray diffraction (XRD), a field emission scanning electron microscope (FESEM), Zeta potential, and Raman spectroscopy. Morphological studies showed single-layered planes with highly porous surfaces, especially PAC activated by NaOH and H2SO4. The results showed that the experimental data were well-fitted with a pseudo-second-order model. Based on Langmuir isotherm, the maximum adsorption capacity for removing methylene blue (MB) was 769.23 mg g-1 and 458.43 mg g-1 for congo red (CR). Based on the isotherm models, more than one mechanism was involved in the adsorption process, monolayer for the anionic dye and multilayer for the cationic dye. Elovich and intraparticle diffusion kinetic models showed that rubber seed shells (RSS) has higher α values with a greater tendency to adsorb dyes compared to rubber seed (RS). A thermodynamic study showed that both dyes' adsorption process was spontaneous and exothermic due to the negative values of the enthalpy (ΔH) and Gibbs free energy (ΔG). The change in removal efficiency of adsorbent for regeneration study was observed in the seventh cycles, with a 3% decline in the CR and 2% decline in MB removal performance. This study showed that the presence of functional groups and active sites on the produced adsorbent (hydroxyl, alkoxy, carboxyl, and π - π) contributed to its considerable affinity for adsorption in dye removal. Therefore, the optimum PAC can serve as efficient and cost-effective adsorbents to remove dyes from industrial wastewater.