| Literature DB >> 35035338 |
Thuan Van Tran1, Duyen Thi Cam Nguyen1,2, Ponnusamy Senthil Kumar3, Azam Taufik Mohd Din4, Aishah Abdul Jalil2,5, Dai-Viet N Vo1,4.
Abstract
Pollution and diseases such as the coronavirus pandemic (COVID-19) are major issues that may be solved partly by nanotechnology. Here we review the synthesis of ZrO2 nanoparticles and their nanocomposites using compounds from bacteria, fungi, microalgae, and plants. For instance, bacteria, microalgae, and fungi secret bioactive metabolites such as fucoidans, digestive enzymes, and proteins, while plant tissues are rich in reducing sugars, polyphenols, flavonoids, saponins, and amino acids. These compounds allow reducing, capping, chelating, and stabilizing during the transformation of Zr4+ into ZrO2 nanoparticles. Green ZrO2 nanoparticles display unique properties such as a nanoscale size of 5-50 nm, diverse morphologies, e.g. nanospheres, nanorods and nanochains, and wide bandgap energy of 3.7-5.5 eV. Their high stability and biocompatibility are suitable biomedical and environmental applications, such as pathogen and cancer inactivation, and pollutant removal. Emerging applications of green ZrO2-based nanocomposites include water treatment, catalytic reduction, nanoelectronic devices, and anti-biofilms.Entities:
Keywords: Biomedical applications; Environmental remediation; Green synthesis; ZrO2 nanoparticles; ZrO2-based nanocomposites
Year: 2022 PMID: 35035338 PMCID: PMC8741578 DOI: 10.1007/s10311-021-01367-9
Source DB: PubMed Journal: Environ Chem Lett ISSN: 1610-3653 Impact factor: 13.615
Fig. 1Green synthesis of ZrO2 nanoparticles and their applications in biomedical, adsorption, catalysis, and nanocomposite fabrication. The plant tissues including flowers, fruits, seeds, leaves, roots, etc. possess many phytochemicals such as polyphenols, saponins, quercetin, and gallic acid. Microorganisms including bacteria, fungi, algae, etc. can secrete biomolecules, metabolites, enzymes, and proteins. These phytochemicals and biomolecules participate in the green synthesis of ZrO2
Fig. 2Extracellularly biosynthesized mechanism of zirconia nanoparticles using Enterobacter sp. strain. Bacteria extracellularly secrete some specific enzymes such as reductase, which take responsibility for enzymatic bioreduction of Zr4+ ions. The underlying mechanism is attributable to the redox of nicotinamide adenine dinucleotide (NAD+/NADH), which supplies electrons to the reduction of Zr4+ ions during nucleation. Capping proteins can also be released into the extracellular environment and aid the biocapping and biostabilization of zirconia nanoparticles. Reprinted with the permission of Elsevier from reference (Ahmed et al. 2021). Abbreviations: ZrONPs, zirconia nanoparticles; NAD+, an oxidized form of nicotinamide adenine dinucleotide; NADH, a reduced form of nicotinamide adenine dinucleotide
Fig. 3Phytochemicals in plant extracts (a), and proposed mechanism for the biosynthesis of ZrO2 nanoparticles using these phytochemicals (b). Phytochemicals act as bioreductants to convert Zr4+ into octahedral complex [Zr(H2O)6]2+. This enhances the stability and hinders the clustering of zirconium complexation during chelation with phytochemicals Zr2+–phytochemicals. The calcination of Zr2+–phytochemicals complex produces ZrO2 nanoparticles in tandem with the release of CO2, H2O, N2, and many decomposed products
Synthesis of green ZrO2 nanoparticles using plants
| Plant extract and zirconium inputs | Complexation step | Calcination step | Refs. | |||||
|---|---|---|---|---|---|---|---|---|
| Plant species | Plant tissue | Zr source | Zr/extract ratio (v/v) | Temperature | Time | Temperature | Time | |
| Roots | ZrOCl2 | 1:1 | Not reported | 3 h | 550 °C | 3 h | Silva et al. ( | |
| Leaves | ZrOCl2 | Not reported | Room | 4 h | 500 °C | Not reported | Gowri et al. ( | |
| Leaves | ZrOCl2 | 1:4 | 70 °C | 1 h | 600 °C | 2 h | Davar et al. ( | |
| Pericarp | ZrOCl2 | 1:1 | 60 °C | 3–4 h | 500–700 °C | Not reported | Alagarsamy et al. ( | |
| Leaves | ZrOCl2 | 1:1 | 75 °C | 3–4 h | 800 °C | Not reported | Al-Zaqri et al. ( | |
| Leaves | ZrOCl2 | 1:1 | Microwave | 15 min | 500 °C | 3 h | Shinde et al. ( | |
| Leaves | ZrOCl2 | 1:1 | 60 °C | 3–4 h | 700–800 °C | Not reported | Annu et al. ( | |
| Seeds | ZrOCl2 | 1:5 | Not reported | 2–3 h | 600 °C | 4 h | Goyal et al. ( | |
| Leaves | ZrOCl2 | 10:1 | 55 °C | 40 min | Not reported | Not reported | Joshi et al. ( | |
| Fruit | Zr(NO3)4 | 7:1 | 180 °C | 18 h | 500 °C | 4 h | Isacfranklin et al. ( | |
| Flower | ZrOCl2 | 2:1 | Not reported | 2 h | 300–500 °C | 3 h | Gowri et al. ( | |
Properties of green ZrO2 nanoparticles
| Green material | Species | Particle size (nm) | Morphology | Crystal phase | Optical band gap (eV) | Surface chemistry | Refs. |
|---|---|---|---|---|---|---|---|
| Alga | 5.0 | Nanosphere | Tetragonal | 4.4 | Hydroxyl, carbonyl, carboxylate | Kumaresan et al. ( | |
| Bacterium | 33–75 | Nanosphere | Not reported | Not reported | Hydroxyl, carbonyl, alkene | Ahmed et al. ( | |
| Bacterium | 44 ± 7 | Nanosphere | Monoclinic, tetragonal | 4.9 | Hydroxyl | Suriyaraj et al. ( | |
| Bacterium | 6.14–15 | Nanosphere | Monoclinic, tetragonal | Not reported | Hydroxyl, zirconium hydroxide | Debnath et al. ( | |
| Fungus | < 100 | Nanosphere | Not reported | Not reported | Hydroxyl, carbonyl, amine | Ghomi et al. ( | |
| Fungus | Not reported | Nanosphere | Tetragonal | Not reported | Hydroxyl, carbonyl | Kavitha et al. ( | |
| Plant | 5.9–8.54 | Nanosphere | Monoclinic, tetragonal | Not reported | Hydroxyl | Silva et al. ( | |
| Plant | < 50 | Nanosphere | Tetragonal | 5.42 | Hydroxyl, carbonyl, zirconium hydroxide | Gowri et al. ( | |
| Plant | 41–45 | Nanochain | Monoclinic, rhombohedral | Not reported | zirconium hydroxide | Sathishkumar et al. ( | |
| Plant | 18–42 | Not reported | Face centered cubic | Not reported | Hydroxyl, carbonyl, amine, alkene | Prasad et al. ( | |
| Plant | 12–17 | Semi-nanosphere | Cubic | Not reported | Hydroxyl, carboxylic, alkyl | Davar et al. ( | |
| Plant | 5–10 | Nanosphere | Tetragonal | 5.535 | Hydroxyl | Alagarsamy et al. ( | |
| Plant | 17 | Nanosphere | Monoclinic, tetragonal | 3.78 | Hydroxyl, alkyl, carboxylic acid | Al-Zaqri et al. ( | |
| Plant | 56.8 | Oval | Tetragonal | Not reported | Hydroxyl, carbonyl, amine | Saraswathi and Santhakumar ( | |
| Plant | 14.7 | Nanosphere | Monoclinic, tetragonal | 4.9 | Hydroxyl, alkyl, carbonyl | Shinde et al. ( | |
| Plant | < 10 | Nanosphere | Not reported | Not reported | Hydroxyl | Annu et al. ( | |
| Plant | 35.45 | Nanosphere | Monoclinic | 3.7 | Carboxyl, alkyl, alkene, amide | Goyal et al. ( | |
| Plant | 20–100 | Nanosphere | Monoclinic, tetragonal | Not reported | Hydroxyl | Chau et al. ( | |
| Plant | 73 | Nanosphere | Not reported | Not reported | Hydroxyl, carbonyl | Joshi et al. ( | |
| Plant | 50 | Nanorod | Monoclinic, cubic | Not reported | Hydroxyl | Isacfranklin et al. ( | |
| Plant | < 150 | Nanoflake | Tetragonal | 5.31 | Not reported | Gowri et al. ( |
Fig. 4Field emission scanning electron microscope photographies of ZrO2 nanoparticles produced at 600 °C without Rosmarinus officinalis leaf extract (a), and from Rosmarinus officinalis leaf extract with the ratio between the extract and zirconium
source 3:1 (b), and 6:1 (c). The role of plant extract is to improve the dispersion of ZrO2 nanoparticles during biosynthesis. Reproduced and adapted with the permission of Elsevier from reference (Davar et al. 2018). Transmission electron microscopy photographs of ZrO2 nanospheres (d), nano chains (e), and nanorods (f) biosynthesized from Acinetobacter sp. bacterial community (Suriyaraj et al. 2019), Curcuma longa tuber extract (Sathishkumar et al. 2013), and Nephelium lappaceum fruit extract (Isacfranklin et al. 2020), respectively. Reproduced and adapted with the permission of Elsevier from references (Sathishkumar et al. 2013; Suriyaraj et al. 2019; Isacfranklin et al. 2020)
Biomedical applications of green ZrO2 nanoparticles
| Green material | Species | Type of activity | Target | Main findings | Ref |
|---|---|---|---|---|---|
| Plant | Antibacterial | Gram negative ( | Zones of inhibition against | Gowri et al. ( | |
| Fungus | Antibacterial | Gram negative ( | Minimum inhibitory concentrations for | Ghomi et al. ( | |
| Plant | Antibacterial | Gram negative ( | Zones of inhibition observed against | Al-Zaqri et al. ( | |
| Strong antibacterial may be due to the flavonoids, protein, tannins, alkaloids, amino acids and carbohydrates present in the leaf extract | |||||
| Plant | Antibacterial | Gram negative ( | Zone of inhibition against | Annu et al. ( | |
| Plant | Antibacterial | Gram negative ( | Zone of inhibition against | Goyal et al. ( | |
| Alga | Antibacterial | Gram negative ( | Zone of inhibition (mm) against | Kumaresan et al. ( | |
| Plant | Antifungal | Bayberry twig blight pathogen | Wide antifungal inhibition zone (25.18 ± 1.52 mm) against | Ahmed et al. ( | |
| Plant | Antibacterial, antifungal | Gram negative ( | Zone of inhibition (mm) against | Chau et al. ( | |
| Plant | Antibacterial, antifungal | Gram negative ( | Zone of inhibition against | Joshi et al. ( | |
| Plant | Anticancer | Human breast cancer cell lines (MCF-7) | Half-maximum inhibitory concentration of 55.32 μg mL−1 | Isacfranklin et al. ( | |
| Plant | Anticancer | Breast cancer cell lines (MCF-7) | The cells viability with 18% inhibition was observed at 500 μg/mL of zirconia nanoparticles | Saraswathi and Santhakumar ( | |
| Nearly 30–40% of the cells showed blebbing |
Fig. 5Synthesis, characterization, and proposed antifungal mechanisms of green zirconia nanoparticles. Green zirconia nanoparticles may pervade through the fungal cell membranes, causing many detrimental effects on ribosomal, chromosomal, and mitochondrial parts. They may change the intracellularly physicochemical properties to cause cell stress and break the integrity of fungal cells. Reprinted with the permission of Elsevier from reference (Ahmed et al. 2021). Abbreviations: TEM, transmission electron microscope; FTIR, Fourier-transform infrared spectroscopy; XRD, X-ray diffraction; EDS, energy-dispersive X-ray spectroscopy; SEM, scanning electron microscopy; UV–Vis, ultraviolet–visible spectroscopy; ZrONPs, zirconia nanoparticles; RNT10, an isolated strain of Enterobacter
Environmental remediation applications of green ZrO2 nanoparticles
| Green material | Species | Type of treatment | Target pollutants | Main findings | Refs. |
|---|---|---|---|---|---|
| Bacterium | Adsorption | Tetracycline | Optimum pH 6.0 | Debnath et al. ( | |
| High adsorption capacity of 526.32 mg/g, adsorption model fitted best with Langmuir model | |||||
| Reusability up to 5 cycles (81.55% after 5th cycle) | |||||
| Plant | Adsorption | Tetracycline | The best adsorptive capacity of 30.45 mg/g was obtained by response surface methodology | Silva et al. ( | |
| Plant | Adsorption | Fluoride | Exothermic and spontaneous adsorption between 20 and 50 °C | Prasad et al. ( | |
| Nearly 99% F– ions were adsorbed by ZrO2-based adsorbent | |||||
| Chemisorption capacity of 96.58 mg/g | |||||
| Plant | Adsorption | Methylene blue | Optimum adsorption conditions at pH 10, adsorbent dosage of 0.3 g, initial methylene blue concentration of 20 mg/L, and average time of 300 min | Alagarsamy et al. ( | |
| 94% removal efficiency for methylene blue dye and adsorptive capacity of 23.26 mg/g | |||||
| Good recyclability: 0.1 M HCl as an efficient eluent, and three consecutive cycles | |||||
| Plant | Catalytic degradation | Reactive yellow 160 dye | 94.58% degradation for Reactive yellow 160 azo dye | Al-Zaqri et al. ( | |
| 0.9837 min−1 for first order rate constant (k1) | |||||
| Plant | Catalytic degradation | Methyl orange | Degradation percentage was at 94.58% after irradiating under the sunlight for 290 min | Saraswathi and Santhakumar ( | |
| Plant | Catalytic degradation | Methylene blue | Optimum conditions: catalyst loading of 1.5 g/L at pH 7 | Shinde et al. ( | |
| Removal of 91.22% after 240 min | |||||
| Plant | Catalytic degradation | Methyl orange | Optimum pH 7 | Shinde et al. ( | |
| Methyl orange was degraded at 69.23% after 240 min |
Potential applications of green ZrO2-based nanocomposites
| Green material | Species | Composites | Properties | Potential applications | Ref |
|---|---|---|---|---|---|
| Plant | Ag/Fe3O4/ZrO2 | Particle sizes: 30–90 nm, saturation magnetization: 10 emu/g | Catalytic reduction of 4-nitrophenol and methyl orange, 3 cycles with swift reaction time (7.5–8 min) | Rostami-Vartooni et al. ( | |
| Plant | CeO2/ZrO2 | Nano-stick like structure (10–15 nm) | Antibacterial against | Pandiyan et al. ( | |
| Narrow band gap (3.37 eV) | |||||
| Plant | Ni-doped ZrO2 | Energy gap of 2.4–2.75 eV | Nanoelectronics | Yadav et al. ( | |
| Plant | Sm-doped ZrO2 (Sm3+/ZrO2+ = 3–11 mol.%) | Highly symmetric nanocubic ( | High stable and reusability with six consecutive recycles | Gurushantha et al. ( | |
| Band gap of 5.3–5.9 eV | High sunlight-driven degradation of Sm/ZrO2 with 11 mol.% dopant against acid green dye | ||||
| Plant | Ag/ZrO2 | Monoclinic and tetragonal phases of ZrO2 | Not reported | Vivekanandhan et al. ( | |
| Face-centered cubic crystal phase of Ag NPs (5–20 nm) on ZrO2 surface | |||||
| Plant | Cu/ZrO2 | Reduced agglomeration of Cu/ZrO2 with particle size of 18–25 nm | Catalytic reduction of 2,4- dinitrophenilhydrazine, various organic dyes such as congo red, nigrosin, methyl orange in the presence of NaBH4 at room temperature | Hamad et al. ( | |
| Cu/ZrO2 exhibited the good stability up to three days after the synthesis process | Ultrafast reaction time for methyl orange (1 s), dinitrophenilhydrazine (40 s), and congo red (150 s) | ||||
| High recyclability at least 5 times | |||||
| Plant | V2O5/ZrO2 | Surface area of 214 m2/g, particle size of 41.74 nm, band gap 3.93 eV | The degradation efficiencies of V2O5/ZrO2 against methyl orange (76.9%) and picloram (86%) for 75 min | Rasheed et al. ( | |
| Thermal stability up to 1000 °C | |||||
| Plant | Ag/ZrO2 | Particle size of 50 nm | The reduction of 2,4-dinitrophenylhydrazine, 4-nitrophenol, nigrosin and congo red | Maham et al. ( | |
| Face centered cubic of Ag on ZrO2 surface | High catalytic performance for reduction of 4-NP into 4-AP (100%) for 6 min, and 2,4-DAPH for 50 s | ||||
| At least 5 cycles for reusability study | |||||
| Plant | Mg-doped ZrO2 | Shape: hollow microspheres, and tetragonal phase | ZrO2–Mg (2 mol.%) gave the highest degradation efficiency (93%) | Renuka et al. ( | |
| Total organic carbon test gave the mineralization rate of 79% after 60 min of reaction | |||||
| Five consecutive cycle runs |
Fig. 6The bioreduction of Ag+ into Ag and nucleation of on ZrO2 surface for the biosynthesis of green Ag/ZrO2 nanocomposites using Anacardium occidentale leaf extract (a); the photograph of as-synthesized green ZrO2 and Ag/ZrO2 nanocomposites (b); scanning electron microscopy (c, d) and transmission electron microscopy (e, f) microphotographies of green Ag/ZrO2 nanocomposites. The presence of leaf extract efficiently leads to the good dispersion and high biostabilization of Ag nanospheres (5–20 nm) on the surface of ZrO2. However, larger addition of leaf extract inhibits the formation of Ag/ZrO2 nanocomposites. Reproduced and adapted with the permission of Elsevier from reference (Vivekanandhan et al. 2015). Abbreviations: AgNP, silver nanoparticles