Antifouling Performance of Carbon-Based Coatings for Marine Applications: A Systematic Review
Abstract
:1. Introduction
2. Results and Discussion
2.1. Study Selection and Characterization
2.2. Graphene-Based Coatings
2.3. Graphene Oxide-Based Coatings
2.4. Carbon-Nanotubes-Based Coatings
2.5. Other Carbon-Nanomaterials-Based Coatings
2.6. Qualitative Assessment
3. Methods
3.1. Search Strategy, Study Eligibility, and Data Extraction
3.2. Quality Assessment
4. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Coating | Material/Matrix | Organism | Experimental Setup | Main Conclusions | Ref. |
---|---|---|---|---|---|
Graphene | Silica | Halomonas spp. | In vitro study Saline solution (0.5 wt%) 20 °C, 72 h | Graphene coatings were effective in decreasing the adhesion and expression levels of adhesion genes of biofilm-producing bacteria Halomonas spp. | [58] |
Silicone rubber | Paracoccus pantotrophus | In vitro study Artificial seawater Quasi-static assay (7 days) Dynamic assay (7 days, varying speeds within the 0.2–0.5 m/s range) | Under quasi-static conditions, the graphene–silicone membranes showed similar AF performance to that of the control surface (rigid polystyrene sheet). Under dynamic conditions, the graphene-based membranes showed better AF performance than the control surface, with around 40% reduction in colony-forming units (CFUs). | [59] | |
Graphene– silver nanocomposites | Silicon | Halomonas pacifica | In vitro study Static assay Marine broth 26 °C, 24 h | The nanocomposite displayed significant bacterial biofilm inhibition (99.6% reduction) and antiproliferative effects on marine microalgae (growth inhibition greater than 80%), whereas surfaces coated with graphene alone did not display any AF properties when compared to the control surface. | [60] |
Dunaliella tertiolecta Isochrysis sp. | In vitro study Provasoli medium 4 days | ||||
Guanidine- functionalized graphene | Boron acrylate polymer | Escherichia coli Staphylococcus aureus | In vitro study Luria–Bertani medium 37 °C, 12 h | The coatings showed excellent antibacterial properties (up to 95% reduction) and diatom antiadhesion rates (up to 99%). The field trial revealed no fouling adhesion or surface deterioration. | [61] |
Phaeodactylum tricornutum Nitzschia closterium f. minutíssima Halamphora sp. | In vitro study F/2 medium 21 °C, 14 days | ||||
Marine micro- and macrofoulers | In situ study Natural seawater (Yellow Sea, China) 2 months | ||||
Laser- induced graphene | Poly(ether)sulfone | Cobetia marina | In vitro study Dynamic assay (65 rpm) Artificial seawater 1 and 36 h | Compared with negative control surfaces, laser-induced graphene coatings showed greater initial bacterial attachment (1 h) but up to 80% less bacterial coverage after 36 h. Initial attachment rates were reduced by the application of negative or positive potential. | [62] |
Graphene Oxide | Alkyd resin | Escherichia coli Staphylococcus aureus Pseudomonas aeruginosa | In vitro study Nutrient medium Room temperature 24 and 48 h | Graphene oxide-coated surfaces greatly reduced bacterial growth (up to 94% loss of cell viability) in vitro and biofouling in situ. | [63] |
Marine micro- and macrofoulers | In situ study Natural seawater (Jeju Sea, South Korea) 3 weeks | ||||
Silicone rubber | Triceratium sp. | In vitro study Algal broth medium 25 °C Static assay (8 days) Dynamic assay (10 days, 3.4 m/s linear velocity near the specimens) | Under static conditions, only one of the tested graphene oxide loadings (0.16 wt%) showed slight diatom antiadhesion effects (approximately 12% OD reduction). In the dynamic assay, only one graphene oxide loading (0.36 wt%) showed diatom antiadhesion properties (approximately 67% OD reduction). | [64] | |
Polymeric membrane calcium ion selective electrode | Marine bacteria | In vitro study Luria–Bertani medium Room temperature 1 h and 5 h | Compared to the noncoated sensor, the proposed graphene oxide-coated sensor displayed significantly improved antiadhesion and bacterial inactivation properties, thus inhibiting the formation of biofilms (around 45% reduction in CFUs). | [65] | |
Graphene oxide–silver nanoparticles | PDMS-silica | Escherichia coli | In vitro study Shaking flask method Saline solution (0.9 wt%) 37 °C, 24 h | The coating containing silver nanoparticles showed improved antibacterial (60% greater inactivation rate) and antialgal (up to 17% reduction in surface coverage) properties, in comparison to pristine graphene oxide. | [66] |
Phaeodactylum tricornutum Navicula torguatum Chlorella sp. | In vitro study Artificial seawater 24 h | ||||
Polypropylene | Halomonas pacifica | In vitro study Static assay Marine broth 26 °C, 24 h | Graphene oxide showed almost no AF properties, while graphene oxide/silver nanocomposites showed more than 80% of biofilm inhibition, as well as no visible fouling by microalgae. | [67] | |
Marine microalgae | In vitro study Adam medium a 1 week | ||||
Graphene oxide–alumina nanorods | PDMS | Micrococcus sp. Pseudomonas putida Aspergillus niger | In vitro study Nutrient-infused medium 35 °C, 28 days | The nanocomposite showed high adhesion resistance for the selected microorganisms (up to around 95% reduction in the number of bacterial cells). | [68] |
Marine micro- and macrofoulers | In situ study Natural seawater 23–28 °C, 3 months | The field trial revealed no fouling or surface deterioration for the nanofilled sample, as opposed to pristine PDMS. | |||
Graphene oxide–silica nanoparticles | PDMS | Pseudomonas sp. Bacillus sp. | In vitro study Nutrient broth 72 h | The coated surfaces showed up to a 4-Log reduction in total viable cells. Analysis of biofilm architecture confirmed a significant reduction of biomass and biofilm thickness on coated surfaces. | [69] |
Freshwater bacterial culture | |||||
Graphene oxide–cuprous oxide nanoparticles | Acrylic resin | Marine micro and macrofoulers | In situ study (0.2–2.0 m below the surface) Natural seawater (South China Sea) Weak water currents (less than 2 m.s−1) 90 and 365 days | Bare panels showed an abundant growth of marine organisms within 90 days, while coated surfaces were hardly fouled by marine organisms after 365 days. | [70] |
Acrylic acid-modified graphene oxide | Acrylic resin | Marine micro and macrofoulers | In situ study Natural seawater (Zhoushan Sea, China) 6 months | Composite-based paint showed great self-polishing AF performance in natural seawater. | [71] |
Polyaniline/p-phenylenediamine-functionalized graphene oxide | Epoxy resin | Organisms in a simulated marine environment (e.g., guppy fish, spirulina algae, and dwarf hair grass) | In vitro study Simulated marine environment 25–27 °C, 3 months | The anticorrosion and AF properties of commercialized epoxy coatings were improved by the addition of the functionalized graphene oxide composite. | [72] |
Reduced graphene oxide | PDMS | Staphylococcus aureus Kocuria rhizophila Pseudomonas fluorescens Pseudomonas aeruginosa | In vitro study Nutrient-infused medium 25 °C, 28 days | In laboratory assays, boehmite nanorod composite coating showed higher antimicrobial activity (endurability percentages for Gram-positive, Gram-negative, and fungi of 86.4%, 97.9%, and 85.9%, respectively) in comparison with bare PDMS and reduced graphene oxide/PDMS. The higher self-cleaning and FR performance of the boehmite nanorod composite coating was confirmed by the field trial. | [73] |
Graphene oxide–boehmite nanorods | Candida albicans Aspergillus brasiliensis | ||||
Marine micro- and macrofoulers | In situ study Natural seawater 23–28 °C, 45 days |
Coating | Material/Matrix | Organism | Experimental Setup | Main Conclusions | Ref. |
---|---|---|---|---|---|
CNTs | Silicone oil-infused epoxy resin | Chlorella sp. Phaeodactylum tricornutum | In vitro study Artificial seawater 22 °C, 21 days | CNTs/epoxy resin coating showed substantially lower algae settlement than bare epoxy resin. Silicone oil-infused CNTs/epoxy resin coating showed even greater inhibition of algae biofilm formation (up to 90% cell reduction). | [74] |
MWCNTs | PDMS | Ulva linza Balanus amphitrite | In vitro study Dynamic assay (similar to the hull of a ship travelling at 15 knots) Artificial seawater 28 °C 45 min for the settlement of zoospores; 7 days for sporeling growth 24 h for initial settlement; 3 months for adhesion strength determination | The release of sporelings was improved by the addition of MWCNTs (approximately 60% of sporeling removal). A significant reduction in adhesion strength of adult barnacles growing on MWCNTs/PDMS was observed. | [75] |
Ulva linza | In vitro study Dynamic assay Artificial seawater 18 °C, 6 days | The incorporation of MWCNTs did not appear to improve the sporeling release properties of PDMS alone. | [76] | ||
Mytilus galloprovincialis (mussels, pediveligers, and plantigrades) | In vitro study Static assay Filtered seawater 18 °C 48 h for pediveligers; 6 h for plantigrades | The incorporation of MWCNTs did not affect mussels’ adhesion or settlement, in comparison to PDMS alone. | [77] | ||
Bacteria and diatoms | In situ study (0.5–1.0 m below the surface) Natural seawater (Zhoushan, China) 28 days | The incorporation of MWCNTs altered the biomass and community composition of biofilms and subsequently decreased mussel settlement (up to around 20% settlement reduction) in comparison to bare PDMS. | [78] | ||
Mytilus coruscus (mussels, plantigrades) | In vitro study Autoclaved filtered seawater 18 °C, 12 h | ||||
Chlorinated rubber | Pioneer eukaryotic biofilm communities | In situ study (1.5 m below the surface) Natural seawater (Xiaoshi Island, China) 10 °C, 312 days | The incorporation of MWCNTs significantly improved AF effects by reducing the diversity and the abundance of pioneer eukaryotic microbes (significantly reduced mean species richness, p < 0.01). | [79] | |
Hydroxyl-modified MWCNTs | Silicone oil-infused PDMS | Marine bacteria | In vitro study Fresh seawater 28 °C, 10 days | Antiadhesion (up to 35% higher removal rate) and AF properties were enhanced, particularly when higher volume ratios of hydroxylated MWCNTs were used. | [80] |
Marine micro- and macrofoulers | In situ study (1–2 m below the surface) Natural seawater (Yellow Sea, China) 8 months | ||||
Carboxyl and hydroxyl-modified MWCNTs | PDMS | Pioneer eukaryotic biofilm communities (such as sea slime, algae sporelings, invertebrates) | In situ study (0.8–1.5 m below the surface) Natural seawater (Xiaoshi Island, China) 2 months | The incorporation of MWCNTs showed excellent AF performance and effectively reduced colonization by pioneer eukaryotes, in comparison to plain PDMS (Shannon diversity index, p < 0.05). | [55] |
Marine micro and macrofoulers | In situ study (1.5 m below the surface) Natural seawater (Weihai Western Port, China) 11 °C, 56 days | The incorporation of a low amount of MWCNTs greatly improved the AF properties of PDMS coatings. However, most modified coatings demonstrated weak modulating effects on pioneer biofilm communities compared to plain PDMS. | [81] | ||
Carboxyl and hydroxyl-modified MWCNTs | PDMS | Pioneer biofilm bacteria | In situ study (1.5 m below the surface) Natural seawater (Xiaoshi Island, China) 10–17 °C, 24 days | All CNT/PDMS composites decreased Proteobacteria biofilm formation, but increased Cyanobacteria biofilm development. | [82] |
Graphitized MWCNTs | |||||
Carboxyl-modified SWCNTs | |||||
Nanomagnetite–hydroxyl-modified MWCNTs | Silicone oil-infused PDMS | Marine bacteria | In vitro study Fresh seawater 28 °C, 24 h | The novel coating exhibited excellent antibiofilm adhesion performance with up to 98% removal rate, compared with PDMS (50% removal rate). | [83] |
Fluorinated MWCNTs | PDMS | Pseudobarnacle adhesion test method | The incorporation of fluorinated MWCNTs improved the FR properties by reducing the pseudobarnacle adhesion strength by 67% compared to bare PDMS, and by 47% compared to pristine MCWNT/PDMS. | [84] | |
Silicon | Escherichia coli | In vitro study Phosphate-buffered saline 37 °C, 6 h | The incorporation of fluorinated MWCNTs showed a decrease of about 98% on CFUs when compared with bare silicon surfaces. | [85] |
Criterion | Mean Score |
---|---|
1. A clearly stated aim: the hypothesis or aim of the study is explicitly and precisely addressed. | 2.00 |
2. Adequate methodology: the methods used to achieve the study’s aim are plausible and clearly described. | 2.00 |
3. Detection of bias: data were collected according to an established protocol. At least 3 replicates or independent experiments were performed for each assay. | 1.93 |
4. Coating: enough information is provided about the tested AF coating. 0: unclear 1: composition is indicated 2: composition AND production method are indicated | 2.00 |
5. Control group: the study uses an appropriate control group, such as bare polymeric coating or uncoated surface. | 1.93 |
6. Surface characterization: the study uses surface characterization methods to assess the coating’s properties. | 1.87 |
7. Type of study: 1: in vitro study 2: in situ OR in vitro study under conditions representative of a real scenario | 1.73 |
8. Experimental setup: sufficiently detailed description of the conditions under which the assays were performed, such as hydrodynamic conditions, culture medium, and temperature. 0: not described 1: incubation time OR culture medium OR temperature is indicated (*) 2: incubation time AND culture medium AND temperature are indicated (*) | 1.90 |
9. Organisms studied: marine fouling organisms used to evaluate the coatings’ AF properties are clearly identified and representative. 0: not described 1: organism species OR organism quantity is indicated (*) 2: organism species AND organism quantity are indicated (*) | 1.76 |
10. Biofilm formation/fouling assay duration: 0: not reported 1: short-term assay (≤48 h) 2: mid/long-term assay (>48 h) | 1.76 |
11. Results clarity: the results of the study are presented in a clear and structured manner. 0: results are not clear 1: results are clear and easy to understand 2: results are clear and easy to understand AND quantitative results (e.g., cell concentration values and adhesion reduction percentage) are reported | 1.83 |
12. Statistical analysis: the study includes the implementation and description of statistical tests appropriate to the dataset. | 0.87 |
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Sousa-Cardoso, F.; Teixeira-Santos, R.; Mergulhão, F.J.M. Antifouling Performance of Carbon-Based Coatings for Marine Applications: A Systematic Review. Antibiotics 2022, 11, 1102. https://doi.org/10.3390/antibiotics11081102
Sousa-Cardoso F, Teixeira-Santos R, Mergulhão FJM. Antifouling Performance of Carbon-Based Coatings for Marine Applications: A Systematic Review. Antibiotics. 2022; 11(8):1102. https://doi.org/10.3390/antibiotics11081102
Chicago/Turabian StyleSousa-Cardoso, Francisca, Rita Teixeira-Santos, and Filipe J. M. Mergulhão. 2022. "Antifouling Performance of Carbon-Based Coatings for Marine Applications: A Systematic Review" Antibiotics 11, no. 8: 1102. https://doi.org/10.3390/antibiotics11081102
APA StyleSousa-Cardoso, F., Teixeira-Santos, R., & Mergulhão, F. J. M. (2022). Antifouling Performance of Carbon-Based Coatings for Marine Applications: A Systematic Review. Antibiotics, 11(8), 1102. https://doi.org/10.3390/antibiotics11081102