Bio-based nanocomposite hydrogels derived from poly (glycerol tartrate) and cellulose: Thermally stable and green adsorbents for efficient adsorption of heavy metals.

The eco-friendly polymeric nanocomposite hydrogels were prepared by incorporating dendritic fibrous nanosilica (DFNS) and apple peel (AP) as reinforcements into the crosslinked polymer produced by cellulose (CL) and poly (glycerol tartrate) (TAGL) via gelation method and used for efficient adsorption of Pb, Co, Ni, and Cu metal ions. DFNS and DFNS/TAGL-CL/AP samples were characterized by FESEM, FTIR, TEM, TGA, and nitrogen adsorption/desorption methods. The results of TGA analysis showed that the thermal stability of the prepared hydrogels improved significantly in the presence of DFNS.

An eco-friendly composite hydrogel based on covalently crosslinked cellulose/poly (glycerol citrate) for thallium (Ι) removal from aqueous solutions.

Cellulose/poly (glycerol citrate) reinforced with thiol-rich polyhedral oligomeric silsesquioxane and apple peel (POSS-SH@CAG-CEL/AP) was synthesized using gelation method in the presence of glutaraldehyde as a crosslinker agent and used as an efficient composite hydrogel for elimination of Tl(Ι) from aqueous solutions. This composite hydrogel and synthesized thiol-rich polyhedral oligomeric silsesquioxane were characterized by elemental analysis, FT-IR, NMR, TGA, and FE-SEM techniques. The effects of synthetic and environmental parameters on the adsorption capacity of the composite hydrogel were investigated and it was found that thiol-rich polyhedral oligomeric silsesquioxane has improved the hydrogel properties including the Tl(Ι) uptake and the thermal stability.

Efficient hydrolysis of starch by α-amylase immobilized on cloisite 30B and modified forms of cloisite 30B by adsorption and covalent methods.

In this paper, α-amylase from Bacillus subtilis was successfully immobilized on three supports. First, α-amylase was immobilized on cloisite 30B via the adsorption method. Then cloisite 30B was activated with tosyl chloride and epichlorohydrin.

Synthesis of a novel superabsorbent with slow-release urea fertilizer using modified cellulose as a grafting agent and flexible copolymer.

In this work, a number of glucose unites in polymeric structure of cellulose was converted to 2,4-dihydroxy-3-(1-hydroxy-2-oxoethoxy)butanal (cellulose containing di aldehyde units (CCDAUs)) by oxidation with sodium periodate, followed by condensation with acetone to produce 5,7-dihydroxy-6-((1-hydroxy-4-oxopent-2-en-1-yl)oxy)hept-3-en-2-one unites (cellulose containing di ene units (CCDEUs)). This modified cellulose was characterized by different methods and applied as a copolymer and grafting agent to synthesize an eco-friendly (CCDEUs-g-poly(AA)/urea) superabsorbent with slow-release urea fertilizer. The created double bonds in C and C positions of β-d-glucose units increased the linkage between cellulose and acrylic acid, leading to the formation of a strong network for slow-release urea fertilizer.

4-(6-Aminohexyl) amino-4-oxo-2-butenoic acid as a novel hydrophilic monomer for synthesis of cellulose-based superabsorbents with high water absorption capacity.

An efficient cellulosic superabsorbent based on a novel functional monomer 4-(6-aminohexyl) amino-4-oxo-2-butenoic acid (AHOB) and acrylic acid was successfully synthesized by free-radical solution polymerization and the effect of the AHOB monomer on the structure, morphology, thermal behavior and viscoelastic features of this superabsorbent was investigated by FTIR, SEM, TGA and rheology methods. Also, the influence of this monomer on the water absorption capacity in various pH and different saline solutions, kinetic behavior, water retention capacity and reusability of the superabsorbent was perused. The results of these experiments confirmed the significant role of the AHOB monomer in improving the properties of the superabsorbent.