Due to rapid industrialization and urban development across the globe, the emission of carbon dioxide (CO2) has been significantly increased, resulting in adverse effects on the climate and ecosystems. In this regard, carbon capture and storage (CCS) is considered to be a promising technology in reducing atmospheric CO2 concentration. Among the CO2 capture technologies, adsorption has grabbed significant attention owing to its advantageous characteristics discovered in recent years. Porous carbon-based materials have emerged as one of the most versatile CO2 adsorbents. Numerous research activities have been conducted by synthesizing carbon-based adsorbents using different precursors to investigate their performances towards CCS. Additionally, amine-functionalized carbon-based adsorbents have exhibited remarkable potential for selective capturing of CO2 in the presence of other gases and humidity conditions. The present review describes the CO2 emission sources, health, and environmental impacts of CO2 towards the human beings, options for CCS, and different CO2 separation technologies. Apart from the above, different synthesis routes of carbon-based adsorbents using various precursors have been elucidated. The CO2 adsorption selectivity, capacity, and reusability of the current and applied carbon materials have also been summarized. Furthermore, the critical factors controlling the adsorption performance (e.g., the effect of textural and functional properties) are comprehensively discussed. Finally, the current challenges and future research directions have also been summarized.

Starch is one of the most common biodegradable polymers found in nature, and it is widely utilized in the food and beverage, bioplastic industry, paper industry, textile, and biofuel industries. Starch has received significant attention due to its environmental benignity, easy fabrication, relative abundance, non-toxicity, and biodegradability. However, native starch cannot be directly used due to its poor thermo-mechanical properties and higher water absorptivity. Therefore, native starch needs to be modified before its use. Major starch modification techniques include genetic, enzymatic, physical, and chemical. Among those, chemical modification techniques are widely employed in industries. This review presents comprehensive coverage of chemical starch modification techniques and genetic, enzymatic, and physical methods developed over the past few years. In addition, the current applications of chemically modified starch in the fields of packaging, adhesives, pharmaceuticals, agriculture, superabsorbent and wastewater treatment have also been discussed.

In this study, two types of modified cassava starch samples (MCS and MWS) prepared from commercially available native cassava starch (NCS) and native cassava starch extracted using the wet method (NWS) were investigated for the removal of Pb(II) ions from aqueous solutions. MCS and MWS samples were synthesized under acidic conditions using Pluronic 123 as the structure-directing agent and tetraethylorthosilicate (TEOS) as the chemical modifying agent. Modified starch samples were characterized using Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), X-ray Diffraction (XRD), and a nitrogen (N2) gas adsorption–desorption analyser. MCS and MWS showed enhanced thermal stabilities upon acid hydrolysis and chemical modification. The effects of contact time and initial Pb(II) concentration were studied through batch adsorption experiments. Adsorption kinetics followed the pseudo-second-order kinetic model. The equilibrium adsorption data were analysed and compared by the Langmuir and Freundlich adsorption models. The coefficient correlation (R2) was employed as a measure of the fit. The Langmuir model fitted well with equilibrium adsorption data, giving a maximum Pb(II) adsorption capacity of 370.37 and 294.12 mg/g for MWS and MCS, respectively. Modified samples exhibited a higher desorption efficiency of over 97%. This study demonstrated that modified starch could be utilized for Pb(II) removal from industrial wastewater.

The health and environmental concerns of the usage of non-biodegradable plastics have driven efforts to explore replacing them with renewable polymers. Although starch is a vital renewable polymer, poor water resistivity and thermo-mechanical properties have limited its applications. Recently, starch/synthetic biodegradable polymer blends have captured greater attention to replace inert plastic materials; the question of ‘immiscibility’ arises during the blend preparation due to the mixing of hydrophilic starch with hydrophobic polymers. The immiscibility issue between starch and synthetic polymers impacts the water absorption, thermo-mechanical properties, and chemical stability demanded by various engineering applications. Numerous studies have been carried out to eliminate the immiscibility issues of the different components in the polymer blends while enhancing the thermo-mechanical properties. Incorporating compatibilizers into the blend mixtures has significantly reduced the particle sizes of the dispersed phase while improving the interfacial adhesion between the starch and synthetic biodegradable polymer, leading to fine and homogeneous structures. Thus, Significant improvements in thermo-mechanical and barrier properties and water resistance can be observed in the compatibilized blends. This review provides an extensive discussion on the compatibilization processes of starch and petroleum-based polymer blends.

Starch and its derivatives have recently emerged as a sustainable and renewable alternative for petroleum-based expanded polystyrene (EPS) and expanded polypropylene (EPP) foam materials. In this study, biodegradable foam materials were prepared from cassava starch using a novel dual modification technique, combining microwave treatment and freeze-drying. The foam materials were prepared from starch solutions microwaved over different intervals. The starch-based foam materials were characterized using Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), 13 C nuclear magnetic resonance ( 13 C-NMR) spectroscopy, and compression set test. Moreover, the water absorption capacities and density values of the foam materials were measured according to ASTM standards. The biodegradability test was carried out according to the aerobic compost environment test. The lowest water absorption capacities of 65.56% and 70.83% were exhibited for the cassava starch foam sample (MWB) prepared at a 20 s microwave treatment time and immersed in distilled water for 2 and 24 h, respectively. Furthermore, the lightweight cassava starch-based foam materials displayed density ranging from 124 to 245 kg/m 3 . The biodegradation test exhibited significant biodegradation of over 50% after 15 days for all the foam materials prepared. These results suggest that the dual-modified cassava starch-based biodegradable foams show potential in sustainable packaging applications by replacing petroleum-based materials.

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Starch is a renewable resource and starch films play a vital role as an alternative for synthetic polymers in packaging applications. However, the films prepared from native starch fail to meet the process or product requirements due to high water absorption and inferior mechanical properties. In order to avoid these drawbacks, and to enhance the desired properties, starch can be modified using acid hydrolysis. In this study, the effects of acid hydrolysis time on the structural, thermal, and chemical properties of cassava starch and cassava starch thin films were investigated. Native cassava starch was hydrolyzed using 2.2 M hydrochloric acid with varying time intervals. With the increase of hydrolysis time, the relative crystallinity of cassava starch increased while the thermal decomposition temperature decreased in cassava starch. XRD and 13C-NMR spectrums results show that, cassava starch has been subjected to polymorphism changes from A (monoclinic cell) to B (hexagonal unit cell) due to the acid hydrolysis treatment. FTIR and TGA analysis showed that, the moisture absorbance of cassava starch decreased significantly as a result of the acid hydrolysis treatment. The acid hydrolyzed samples showed up to 31.79 % reduction of moisture content compared to the native starch samples. Also, the films prepared from acid hydrolyzed starch showed up to 25.12% reduction of water absorption compared to that prepared from native starch. Acid hydrolysis treatment significantly impacted the mechanical behavior of starch-based films. The tensile strength of cassava starch-based films improved continuously with acid hydrolysis time, reaching a maximum of 5.67 MPa. However, the ductility of the films was negatively impacted when the starch was subjected to acid hydrolysis. The films prepared using acid hydrolyzed starch showed a 12.78 % reduction of elongation compared to that prepared with native cassava starch, despite with minimum dependence of acid hydrolysis time.