Development of an environmentally sustainable technique to minimize the sludge production in the textile effluent sector through an electrokinetic (EK) coupled with electrooxidation (EO) approach.

This study presents an environmentally sustainable method for minimizing sludge production in the textile effluent sector through the combined application of electrokinetic (EK) and electrooxidation (EO) processes. AAS and XRF analyses reveal that utilizing acidic electrolytes in the EK method successfully eliminates heavy metals (Cu, Mn, Zn, and Cr) from sludge, demonstrating superior efficiency compared to alkaline conditions. In addition, the total removal efficiency of COD contents was calculated following the order of EK-3 (60%), EK-1 (51%) and EK-2 (34%). Notably, EK-3, leveraging pH gradient fluctuations induced by anolyte in the catholyte reservoir, outperforms other EK systems in removing COD from sludge. The EK process is complemented by the EO process, leading to further degradation of dye and other organic components through the electrochemical generation of hypochlorite (940 ppm). At an alkaline pH of 10.0, the color and COD removal were effectively achieved at 98 and 70% in EO treatment, compared to other mediums. In addition, GC-MS identified N-derivative residues at the end of the EO. This study demonstrates an integrated approach that effectively eliminates heavy metals and COD from textile sludge, combining EK with EO techniques.

Biodegradation of pyrene by bacterial consortia: Impact of natural surfactants and iron oxide nanoparticles.

Polycyclic aromatic hydrocarbons (PAHs) are potentially hazardous compounds that could cause a severe impact on many ecosystems. They are very challenging to remove using conventional methods due to their hydrophobic nature. However, this issue can be resolved by utilizing surface-active molecules to increase their bioavailability. In this study, pyrene was chosen as the PAH compound to explore its degradability by the effect of individual bacterial strains (Pseudomonas stutzeri NA3 and Acinetobacter baumannii MN3) and mixed consortia (MC) along with natural surfactant derived from Sapindus mukorossi and iron oxide nanoparticles (NPs). Additionally, fatty acids esters, dipeptides, and sugar derivative groups were identified as potent bioactive components of natural surfactants. Various techniques, such as XRD, VSM, TEM, and FE-SEM with EDX, were utilized to characterize the pristine and Fenton-treated iron oxide NPs. The analytical results confirmed that the Fe3O4 crystal phase and spherical-shaped NPs exhibited excellent magnetic properties. The impact of natural surfactants and iron oxide NPs has significantly contributed to the biodegradation process, resulting in a prominent decrease in chemical oxygen demand (COD) levels. Gas chromatography-mass spectrometry (GC-MS) analysis showed that biodegradation systems produced primary hydrocarbon intermediates, which underwent oxidative degradation through Fenton treatment. Interestingly, synthesized iron oxide NPs effectively produced hydroxyl radical (•OH) during the Fenton reaction, which was confirmed by electron paramagnetic resonance (EPR) spectra, and the pristine iron oxide NPs underwent a material transformation observed. The study demonstrated an integrated approach for biodegradation and the Fenton reaction process to enhance the pyrene degradation efficiency (90%) compared to other systems. Using natural surfactants and iron oxide NPs in aquatic environments serves as a crucial platform at the interface of microorganisms and contaminated oil products. This interaction offers a promising solution for PAHs bioremediation.

Metagenomics diversity analysis of sulfate-reducing bacteria and their impact on biocorrosion and mitigation approach using an organometallic inhibitor.

Sulfate-reducing bacteria (SRB) have impacted the biocorrosion process for various industrial sectors, especially in the oil and gas industry. The higher stability over extreme conditions is the key parameter for their survival in such environments. So far, many materials have been tried to minimize or control the growth of SRB. In the present study, an organo-metallic compound of the zinc sorbate (ZS) was successfully synthesized by the simple co-precipitation method and its improved antibacterial activity against SRB. The SRB consortia are enriched from the sub-surface soil sample and identified by 16s rDNA sequencing by targeting the V3-V4 region. The most dominating genera identified with sulfate-reducing capability are Sulfurospirillum (42 %), Shewanella (19 %) Bacteroides (14 %), and Desulfovibrio (8 %). Further biocorrosion experiments are conducted by weight loss methods. Higher corrosion current density (Icorr) and less charge transfer resistance (Rct) are observed for the SRB consortia. Concurrently, higher Rct is kept for the inhibitor-included systems. The slowest release of the sorbate into the medium suppressed the growth of the SRB bacterial cells with 86 ± 3 % corrosion inhibition efficiency and prevented further corrosion reactions by forming a protective layer over the surface of the carbon steel API 5LX. The surface analysis strongly confirmed that SRB caused pitting corrosion, which has been suppressed in the inhibitor-included systems.

Bio-approach: preparation of RGO-AgNPs on cotton fabric and interface with sweat environment for antibacterial activity.

This study aims to develop a reduced graphene oxide (RGO)-silver nanoparticles (AgNPs) coating on the cotton fabric (CT) surface using photoreduction with a hydrothermal process and evaluate the antibacterial activity in a sweat environment. An ureolytic bacterium of Bacillus subtilis (HM475276) was used to generate ammonia from synthetic urine. RGO-AgNPs were synthesized on the CT surface using a moderate dosage of 1% silver ammonium complex. The analytical study reveals that spherical-shaped AgNPs of 10-50 nm size were uniformly anchored throughout the RGO sheet on the CT, further supported by X-ray photoelectron spectroscopic analysis (XPS). X-ray powder diffraction (XRD) and Energy-dispersive X-ray absorption spectroscopy (EDAX) elemental mapping confirmed Ag/AgCl formation on CT treated with sweat. The sustained release of Ag+ ions from the treated CT in the sweat solution was assessed by atomic absorption spectroscopy (AAS) and ranged from 2 to 8 ppm, correlated with antibacterial activity. The agar diffusion and solution suspension method to demonstrate the combat bacterial species were greater on RGO-AgNPs-CT than sweat-treated CT due to the suppression of Ag+ ion release caused by the deposition of Ag/AgCl. Hence, sweat-treated RGO-AgNPs-CT proved to have higher inactivation activity (45 min) than sweat-treated AgNPs-CT (60 min) due to the RGO-Ag/AgCl serving photocatalyst influencing hydroxyl radical (OH·) formation under sunlight. The RGO-AgNPs-CT has confirmed that it retains antibacterial activity after passing the laundry durability test. Together, the results showed an opportunity for improved functional fabrics that are exceptional at combating bacterial pathogens and holding up well to laundry durability tests.

Impact of biosurfactant and iron nanoparticles on biodegradation of polyaromatic hydrocarbons (PAHs).

Polycyclic aromatic hydrocarbons (PAHs) are hazardous toxic contaminants and considered as primary pollutants due to their persistent nature and most of them are carcinogenic and mutagenic. The key challenge in PAHs degradation is their hydrophobic nature, which makes them one of the most complex materials and inaccessible by a broad range of microorganisms. This bioavailability can be increased by using a biosurfactant. In the present study mixed PAHs were degraded using the biosurfactant producing bacterial strains. In addition, iron nanoparticles were synthesized and the impact of iron nanoparticles on the growth of the mixed bacterial strains (Pseudomonas stutzeri NA3 and Acinetobacter baumannii MN3) was optimized. The mixed PAHs (anthracene, pyrene, and benzo(a)pyrene) degradation was enhanced by addition of biosurfactant (produced by Bacillus subtilis A1) and iron nanoparticles, resulting in 85% of degradation efficiency. The addition of the biosurfactant increased the bioavailability of the PAHs in the aqueous environment, which might help bacterial cells for the initial settlement and development. The addition of iron nanoparticles increased both bacterial biomass and PAHs adsorption over their surface. These overall interactions assisted in the utilization of PAHs by the mixed bacterial consortia. This study illustrates that this integrated approach can be elaborated for the removal of the complex PAHs pollutants from soil and aqueous environments.

Biological mediated synthesis of RGO-ZnO composites with enhanced photocatalytic and antibacterial activity.

In this study, we reported the biological approach to synthesis of ZnO nanorod (NR) on the reduced graphene oxide (RGO) for photocatalytic, antibacterial activity and hydrogen production under sunlight. Bacillus subtilis played a vital role in the production of biogenic ammonia from synthetic urine and utilized for the synthesis of ZnONR on the RGO sheet. The morphological study revealed that RGO sheets displayed a tremendous role in anchoring ZnONR. XRD patterns showed the ZnO crystal phase on the RGO sheets. XPS and Raman spectra confirmed that the bio-hydrothermal method as suitable for GO converted into RGO. The transient photocurrent and I/V measurement are exhibited as an increment on the RGO-ZnONR compared to ZnONR. The RGO-ZnONR composites showed excellent performance with decolorization of MB and textile dyes and efficient control of the E. coli and S. aureus. RGO-ZnONR exhibited remarkable noted as a higher photocatalytic hydrogen evolution rate (940 µmol/h/gcat) than the ZnONR (369.5 µmol/h/g cat). As a result of photocatalytic performance to correlate with sunlight intensity was extensively studied. RGO plays an essential role in interface electron transfer from sunlight to ZnONR for enhancing •OH radical formation to cleavage of dye color substance and eradicated bacterial cells.

Novel synthesis of ZnO by Ice-cube method for photo-inactivation of E. coli.

The ZnO particle with varieties of morphology was prepared from ice-cube of zinc ammonium complex at boiling water surface in 1 min induction of thermal shock. The zinc ammonium complex in ice cube was developed using zinc acetate and biologically activated ammonia in 1 hr and kept in the freezer. Temperature gradient behaviour of the water medium during thermal shock was captured by the thermal camera and thermometer. Morphology study revealed a variety of flower-like ZnO particles with variable size from 1.0 to 2.5 µm. Further, ZnO particle morphologies were tuned by adding trisodium citrate and hexamine to obtain uniform spherical (2-3 µm) and flower (3-4 µm) shapes, respectively. XRD patterns revealed that all ZnO samples are of a hexagonal structure. Photocatalytic inactivation of E. coli has been investigated using various particle morphologies of ZnO in an aqueous solution/overcoated glass slide under sunlight. The photo-inactivation of E. coli by ZnO particles in suspension condition was better when compared to a coated glass slide method. AFM study confirmed the destruction of bacterial cell wall membrane by the photocatalytic effect. The particles morphology of photocatalyst is well dependent on antibacterial activity under sunlight.

A Strategy to Develop Bioactive Nanoarchitecture Cellulose: Sustained Release and Multifarious Applications.

Cellulose membranes were engineered to produce hydrophobic surfaces via a simple and soft chemical process to introduce multifunctional properties of an otherwise hydrophilic cellulose surface with polymer-grafted nanosilver to form a core-shell nanostructure. A superhydrophobic domain of the polymer on cellulose was created through the amide bond formation between the anhydride units of the polymer and the aminosiloxane-functionalized cellulose through layer-over-layer formulation. This formulation was confirmed through XPS, XRD, 29Si-NMR, and FTIR studies. Further, SEM and TEM analysis revealed that short linear silver nanowires were uniformly obtained with an average diameter of 60 nm and length of 288 nm, using a mild reducing agent at 60 degrees C, which resulted in a hierarchical cellulose surface. The nanosilver colloids released from the hierarchical cellulose surface were stabilized by the polymer matrix in solution, which led to a decrease in the rate of formation of Ag+ enhancing the material's killing efficacy against microbes. This biodegradable nanocomposite-based cellulose hierarchical surface development has potential for application as superhydrophobic membranes for oil-water separation, antimicrobial activity, and pH-triggered sustained release of colloidal silver for wound healing, which could possibly be applied for use as smart bandages.

Bio-mediated synthesis of TiO2 nanoparticles and its photocatalytic effect on aquatic biofilm.

The nano-TiO(2) was synthesized biologically employing Bacillus subtilis (FJ460362). These nanoparticles were characterized by FTIR, TGA-DTA, UV-Visible spectroscopy, XRD and TEM. FTIR and TGA results confirm that the organic impurities were completely removed while calcinating the resultant products. Band gap value was estimated from the UV-Visible spectrum and anatase crystal phase was confirmed by XRD. TEM images reveal that these particles were agglomerated; mostly spherical in shape with an average particle size of 10-30nm. The synthesized nano-TiO(2) particles were coated on glass slides, biofilm were grown and subjected to irradiation of polychromatic light to understand photocatalytic activity in controlling the aquatic biofilm. The bacterial killing process was established by Epi-fluorescence microscopy. The results reveal that biogenic TiO(2) nanomaterial acts as good photocatalyst by the generation of H(2)O(2) in the vicinity of the TiO(2)-biofilm interfaces to suppress the growth of the aquatic biofilm.

Biosynthesis of calcium hydroxylapatite coating on sputtered Ti/TiN nano multilayers and their corrosion behavior in simulated body solution.

Titanium/titanium nitride (Ti/TiN) nanoscale multilayered films were deposited onto 316L stainless steel substrates by reactive magnetron sputtering using a Ti target. Coatings characterized by X-ray diffraction showed that the stack possesses centered cubic structure. The X-ray photoelectron spectroscopy survey spectra on the etched surfaces of the stack film on steel exhibited the characteristic Ti2p, N1s, and O1s peaks at the corresponding binding energies 454.5, 397.0, and 530.6 eV, respectively. Platelet adhesion experiments were carried out to examine the interaction between blood and the materials in vitro. The results indicated that the smoothness and lower isoelectric point contribute to better hemocompatibility of the Ti/TiN nanoscale multilayered coating. The biomediated synthesis of calcium hydroxylapatite (HA) was carried out on coated substrates using calcium-depositing bacteria. The observation of low corrosion current density (I(corr)) for the calcium HA-coated Ti/TiN specimens in simulated body fluid confirmed their highly resistive nature under the testing condition.