pH Adjustment Research Articles

New Insight into Mercury Removal from Fish Meat Using a Single-Component Solution Containing cysteine.

A novel approach for reducing mercury content in fish meat during post-packaging storage is developed to extend the margin of their safe consumption. It involves employing a single-component aqueous medium containing cysteine, as the active agent responsible for displacing mercury from fish proteins and its stabilization in the medium without the need for pH adjustments. The mercury removal efficiency depends on the cysteine concentration and its ratio to fish muscle. Using 1.2wt% cysteine enables a reduction of mercury in canned Albacore tuna by 25-35%, depending on the fish product type and the exposure time of up to 2 weeks. The potential for the successful application of the developed method in active food packaging solutions is studied for the simultaneous or subsequent purification of the extraction solution through adsorption. Using thiolated silica could potentially enable the extraction process but it is shown that the presence of cysteine significantly hinders the adsorption.

Influence of pH and salt conditions on extraction efficiency and functional properties of Macrotermes nigeriensis protein concentrate for food applications

The search for alternative proteins from non-conventional sources for food processing has become important due to the shortage of conventional protein sources. Protein extractability from Macrotermes nigeriensis and its functional properties were investigated under various conditions of pH (2–10) and salt concentration (0.1–1.0 M). Extracted proteins were precipitated through pH adjustment and micellization, respectively. Results showed that maximum protein extractability was 68% and 62.1% at 0.5 M salt concentration and pH10.0, respectively. Salt-extracted protein-rich fraction (SP) had the highest protein composition (68.68 ± 0.41 g/100 g), seconded by alkaline-extracted protein-rich fraction (AP) (62.91 ± 0.53 g/100 g), compared with the raw and defatted fraction (34.36 ± 0.44 and 42.12 ± 0.15 g/100 g), respectively. The highest emulsion capacity (49%) and emulsion stability (35%) were recorded in alkaline pH 10.0. In comparison, the highest foaming capacity (24%) and foaming stability (16%) were recorded in the salt-extracted fraction at 6%. This information could be useful for further studies on the food application potential of proteins isolated from edible M. nigeriensis.Graphical

Enhancing phosphorus removal: the impact of alkaline environment in eutrophic water systems

Abstract Excessive phosphorus input leads to poor water quality and eutrophication. However, limited research has directly explored the influence of pH on phosphorous in actual aquatic systems. This study investigated the effect of pH on phosphorus removal in synthetic, eutrophic, and black-odorous water. The pH levels ranging from 3.5 to 12.0 were adjusted using H2SO4, NaOH, and cement with a 0.5 ± 0.03 interval, followed by a 25 ± 1 °C static water bath for 24 h. Results showed that NaOH-adjusted pH removed >65% TP from eutrophic water (pH ≥9.50) and black-odorous water (pH ≥11.0). Meanwhile, cement-adjusted pH removed >84%, >90%, and >82% TP from the synthetic solution (pH ≥11.0), eutrophic water (pH ≥9.5), and black-odorous water (pH ≥9.5), respectively. The alkaline environment enhanced the formation of Ca-P in eutrophic water and black-odorous water, and cement strengthened the chemical precipitation of phosphorus by providing additional Ca2+. This study lays the groundwork for pH adjustment strategies in eutrophic water, holding significant implications for water resource management and environmental protection.

Active Polysaccharide-Based Films Incorporated with Essential Oils for Extending the Shelf Life of Sliced Soft Bread.

Active, fully biobased film-forming dispersions (FFDs) with highly promising results for sliced soft bread preservation were successfully elaborated from carboxymethyl cellulose (CMC) and chitosan (CH) using a simple method based on pH adjustments. They consisted of the association of polysaccharides and oleic acid (OL) added with cinnamon (CEO) or ginger (GEO) essential oils. The chemical compositions of the commercial essential oils were first determined via GC/MS, with less than 3% of compounds unidentified. The films obtained from FFDs were characterized by SEM, FTIR and DSC, indicating specific microstructures and some interactions between essential oils and the polymer matrix. CEO-based films exhibited higher antioxidant properties and a lower minimal inhibitory concentration in terms of antifungal properties. From experiments on sliced soft bread, the ginger-based films could increase the shelf life up to 20 days longer than that of the control. Even more promising, cinnamon-based films led to complete fungal inhibition in bread slices that was maintained beyond 60 days. Enumeration of the yeasts and molds for the FFD-coated breads revealed complete inhibition even after 15 days of storage with the FFDs containing the highest concentration of CEO.

The Synergistic Power of Rosehip Seed Powder and Aluminum Chloride in Steel Industry Wastewater Treatment

This study investigates the efficiency of a hybrid coagulation–flocculation process for the treatment of industrial wastewater from the steel industry. The novel method combines a natural coagulant, processed Rosehip Seed Powder (RSP), with a chemical coagulant, aluminum chloride (AlCl3), across varying concentrations and pH levels. The study simulated the pH 8 conditions of iron and steel industrial wastewater and examined the removal of heavy metals, total suspended solids (TSS), chemical oxygen demand (COD), and ammonia–nitrogen (NH3-N). At pH 8, the optimal coagulant dosage was determined to be 0.75:0.75 (g/g) of RSP/AlCl3 powder, resulting in high removal efficiencies across several parameters: 88.29% for COD, 91.85% for color, 99% for TSS, 93.11% for NH3-N, 94.3% for Mn, 98.5% for Fe, 96.7% for Zn, and 99.3% for Ni. The pH optimization demonstrated high removal efficiencies without pH adjudication. The removal of heavy metals at pH 8 demonstrated high efficiencies, with Mn, Fe, Zn, and Al achieving 99.00%, 90.6%, 95.73%, and 92.3%, respectively. These results suggest that no pH adjustment is required when using RSP/AlCl3 for the treatment of iron and steel industry wastewater through the coagulation method.

Natural deep eutectic solvent-based dispersive liquid-liquid microextraction of pesticides in drinking waters combined with GC-MS/MS detection

The current research aims to develop a new analytical method applying a dispersive liquid-liquid microextraction (DLLME) assisted by vortex and using an environmentally friendly extractant for the preconcentration of organochlorine and organophosphorus pesticides followed by gas chromatography-tandem mass spectrometry (GC-MS/MS) analysis. The extractant (i.e., natural deep eutectic solvent (NADES)) is safe, cheap, biodegradable and can be prepared by simply mixing DL-menthol and decanoic acid (molar ratio 2:1). The main experimental factors affecting the extraction of all analytes evaluated (19 organochlorine and organophosphorus pesticides) have been optimised using a multivariate analysis consisting in two steps: a Plackett-Burman design followed by a central composite design (CCD). Seven experimental factors have been evaluated: (i) sample volume; (ii) NADES volume; (iii) sample pH; (iv) extraction time; (v) centrifugation time; (vi) centrifugation speed; and (vii) ionic strength (NaCl %, w v−1). For the significant variables, the optimum values were 10 mL sample and 45 μL NADES. No pH adjustment as well as addition of NaCl were needed. The other variables were set at 3 min extraction time, 5 min centrifugation time and 900×g centrifugation speed, respectively. Under the optimised extraction conditions, the limit of quantification (LOQ) values ranged between 0.2 and 78 ng L−1 for all analysed pesticides. Furthermore, the proposed analytical method has been successfully applied to drinking water (bottled spring water). The recovery study (n = 3) has been evaluated at 0.1, 1.0 and 5.0 μg L−1 spiking levels, obtaining relative recovery values within the range of 70 % and 117 % and RSD values between 1 % and 20 % for all the analytes studied, except for p,p-DDT (56–77 % in high conductivity water samples).

Advanced, Cutting-Edge RP-HPLC Methodology for the Comprehensive Quantitative Analysis of Assay of Bictegravir, Emtricitabine, and Tenofovir Alafenamide in Co-Formulated Pharmaceutical Products.

In the current study, a simple and economic stability-indicating RP-HPLC method development and validation was carried out to estimate the bictegravir, emtricitabine and tenofovir from the pharmaceutical dosage form. 0.1M ammonium acetate in 0.5% v/v acetic acid solution and 1g of 1-octane sulfonic acid and adjustment of pH to 4.2 with dilute orthophosphoric acid done and methanol (40:60 v/v) was utilized as the mobile phase. The analysis was done using Inertsil ODS 3V (250 x 4.6 mm x 5 µm) column with column temperature kept at 30°C with an injection volume of 20 μL, flow rate of 1.0 ml/ minute and detection was carried out at 260 nm. The method was developed and it was validated according to ICH Q2 (R1) guidelines. The RT of bictegravir, emtricitabine and tenofovir were determined to be 12.23, 3.0 and 8.5 minutes, providing a reliable marker for its identification. The method was found linear from about 50 To 150% Of the target concentration of bictegravir emtricitabine and tenofovir with of 0.999. Significant degradation was observed in acidic, basic and peroxide stress conditions. Hence, it can be concluded that tablets are sensitive to acidic, basic and oxidation stress conditions. RSD for the peak area responses of emtricitabine, 0.03 and 0.03, respectively, indicating that the system is precise. The testing procedure was accurate from about 50 to 150%. Of the target concentration of emtricitabine, tenofovir alafenamide and bictegravir. The method was robust In relation to flow variation, column oven temperature variation, mobile phase variation and pH variation. In conclusion, our proposed RP-HPLC method provides a sensitive, accurate, and precise means of analyzing emtricitabine, tenofovir alafenamide and bictegravir from pharmaceutical dosage forms.

Integrated Recovery of Iron and Nickel from Olivine Ores Using Solvent Extraction: Synergistic Production of Amorphous Silica and Carbonates through pH Adjustment and Carbon Mineralization

Integrated Recovery of Iron and Nickel from Olivine Ores Using Solvent Extraction: Synergistic Production of Amorphous Silica and Carbonates through pH Adjustment and Carbon Mineralization

Evaluation of calcium carbonate production and cementitious characteristics of enzymatically induced carbonate precipitation during environmental adjustment

Enzymatically induced carbonate precipitation (EICP) is an emerging and eco-friendly technology, which is considered a green alternative to traditional cement in soil stabilization. When stabilizing soil use one-phase grouting method, the activity of urease is often adjusted, leads to changes in the composition and cementitious characteristics of CaCO3. Previous studies primarily focused on the mechanical properties of solidified soil samples, while the production and cementitious characteristics of CaCO3 influenced by the control of urease activity is rarely discussed. This study investigated production and cementitious characteristics of CaCO3 under different reaction environment (pH adjustment, temperature adjustment, and addition of inhibitors), during which the urease activity tests, pH tests, CaCO3 production tests and ultrasonic oscillation tests are conducted. Meanwhile, the morphological characteristics and mineral composition of CaCO3 are revealed through Scanning Electron Microscope-Energy Dispersive Spectrometer (SEM-EDS) tests and X-ray Diffraction (XRD) test. The results demonstrate that all three one-phase grouting methods can delay the production of CaCO3 at early-stage of EICP, while the pH should be maintained above 4 to prevent significant urease deactivation. The CaCO3 generated in EICP mainly consists of calcite and vaterite, and the size of CaCO3 increases with the urease activity increased. The cementitious characteristics of CaCO3 is mainly determined by the percentage composition of calcite and vaterite, where higher vaterite content results in weaker cementitious characteristics. This study provides insights for evaluating the cementitious characteristics of CaCO3, which is beneficial for guiding the promotion and application of one-phase grouting method.

Removal of refractory humic acid-like components from UF filtrate of landfill leachate through pH adjustment and coupled electrochemical process

Mature landfill leachate contains large quantities of a wide range of hazardous and refractory pollutants, especially humic acid-like (HA) and fulvic acid-like (FA) substances. These have poor biodegradability and a considerable ultraviolet-light quenching capacity, severely inhibiting the performance of wastewater treatment and post ultraviolet-light disinfection, but this aspect has attracted little previous research. The Fenton reaction has proved to be a feasible method for removing ultraviolet-quenching substances (UVQSs) but in conventional systems it is unable to completely mineralize organic contaminants. In this study, a novel electro-oxidation process was developed consisting of a flow-through reactor with a Cu2O cathode to catalyze Fenton-type reactions, and oxidation at a RuO2 anode. The combination of pH adjustment and electro-oxidation was evaluated for the treatment of real ultrafiltration (UF) filtrate of mature landfill leachate. A series of analytical techniques were used to determine the performance for the removal of HA and FA. Under optimal conditions, the elimination of fluorescence characteristics of HA and FA reached 100 % and 99.3 %, respectively, according to PARAFAC results based on EEM spectra. TOC was removed by 25.5 %∼30.4 % during the pH adjustment step and 51 % by electrochemical oxidation. Changes in the molecular weight distribution and fluorescence content showed that pH adjustment played an important and significant role in removing UVQSs, and the remaining TOC after electrochemical oxidation was attributed to bioavailable amino acid-like substances. Overall, the results have demonstrated the successful development of an effective method of treating the UF filtrate from mature landfill leachate, with particular respect to the removal of the problematic HA and FA content.

Optimization of potassium (K) recovery via electrochemical precipitation of K-struvite upon magnesium addition in urine

Potassium (K)-struvite precipitation is a promising approach to K recovery but faces the critical challenge of co-precipitation of sodium (Na)-struvite mainly due to the addition of sodium hydroxide (NaOH) for pH adjustment. To avoid using NaOH, this study investigated the electrochemical addition of magnesium (Mg) and hydroxide ions for K-struvite recovery. Results showed that a high release rate of Mg and hydroxide ions in the electrolysis led to a Mg:Phosphorus (P) ratio higher than 1:1 and pH higher than 11.3, which however resulted in a decrease in the K recovery efficiency. Subsequent optimization experiments conducted in synthetic urine, diluted fivefold, maintained a process pH of 10.811.0, with a current density of 5 mA/cm2 and an electrode spacing of 20 mm. Under these conditions, K recovery efficiency reached 38 %, while P recovery efficiency reached 93 % after 30 minutes of electrolysis. Compared to chemical precipitation methods, electrochemical recovery exhibited a 41 % increase in K recovery efficiency and a 153 % increase in K-struvite:Na-struvite molar ratio in the precipitates. Furthermore, a predictive model was developed to estimate optimal K recovery time and energy consumption, showcasing the effectiveness of electrochemical Mg addition in urine for high-efficiency K recovery.

Efficient recovery and utilization of phosphorus from sewage sludge via alkalinous fenton-like oxidation with pyrolysis-modified red mud: Full resource utilization attempt

Red mud (RM) and sewage sludge (SS) are growing massive industrial wastes, and recycling utilization is considered a suitable disposal method. In this study, a novel Fenton-like catalyst was synthesized through co-pyrolysis with RM and SS with high alkaline endurance, presenting a sustainable full resource utilization of the SS. The advanced oxidation process effectively breaks down the SS structure to release phosphorus(P) for struvite recovery. The residual SS can be repurposed as fuel following direct flocculation and dehydration. There is no need for complex pH adjustments throughout. XRD pattern revealed zero valent iron (ZVI, Fe0) as the primary catalyst phase. Experimental findings demonstrated that H2O2 efficiently disrupts bacterial structures, leading to a significant reduction in bound extracellular polymer (TB-EPS) in the SS. It was observed that the release rate of P reached nearly 100% after 60 min of reaction. The purity of recycled struvite reaches 94.9%, and the heavy metal content meets national standards. Planting experiments indicated that recycled struvite exhibited superior fertility compared to commercial fertilizers. The proposed sustainable resource production and recycling process of SS strongly supports the construction of a "city without waste".

Synergistic mechanism of pH control by CO2 and CaO2 pre-oxidation to enhance algae dehydration

This study investigated the improvement of algal dehydration efficiency through CO2 pH adjustment and moderate pre-oxidation with CaO2 to enhance coagulation. Adjusting the pH of algal water to 6.0–9.5 with CO2 significantly affected zeta potential and photosynthesis, enhancing aluminum hydrolysis product aggregation. At pH 6.5, the composition of algal organic matter closely matched the original water, indicating minimal impact on algae and optimal cell activity. CaO2 pre-oxidation effectively reduced residual aluminum content and DOM release after coagulation. The DOM removal rate reached 44.50 % at pH 6.5, with the highest dehydration efficiency of 44.34 % and the lowest cell rupture rate of 5.55 %. Small molecular aromatic proteins decreased, while humic substances increased significantly. The chemical bonding between the EPS membrane and CaO2 improved system density and elasticity, enhancing dehydration performance. This study provides new insights and guidance for the ongoing study of pH and CaO2 enhanced algal dehydration.

Valorization of coffee agro-industrial residue for biochar production: Use as adsorbent for methylene blue removal

This research explores using thermally modified residual coffee grounds as a bioadsorbent for removing methylene blue (MB) from aqueous solutions. The study investigates the impact of pH on adsorption capacity, emphasizing its significant influence. Kinetic studies reveal that the pseudo-first-order (PFO) model accurately describes the MB removal process, with correlation coefficients (R²) close to 1 for all samples. The Freundlich model provided the best fit for residual coffee grounds, while the Langmuir model was most suitable for biochar 1. The BiDR model provides the best fit with high R² values, indicating efficient removal for biochar 2 and biochar 3. Notably, the research shows that MB adsorption is effective without requiring pH adjustments, thereby reducing environmental impacts. The maximum adsorption capacities were 40.85, 20.35, 19.52 and 41.98 mg.g−1 using residual coffee grounds, biochar 1, biochar 2 and biochar 3, respectively. Overall, this study demonstrates the practicality of using thermally activated coffee grounds as an efficient adsorbent for removing textile dyes from effluents and highlights the potential of alternative uses for coffee grounds and biochar residues in environmental applications.

Integration of CO2 sequestration with the resource recovery of red mud and carbide slag

Red mud and carbide slag, strongly alkaline solid wastes, are produced during the manufacturing of alumina and acetylene gas, respectively. Improper management of these wastes can pose significant environmental hazards. This study proposed a novel method for the collaborative treatment of red mud and carbide slag, enabling the recovery of constituent elements with CO2 sequestration. During the hydrochloric acid leaching process, Si was reclaimed as Si-rich residue, whereas Ti, Al, Ga, Fe, and Sc were stepwise recovered as Ti-rich product, Al/Ga-rich filtrate, and Fe/Sc-rich product via the subsequent hydrolysis, co-precipitation, and alkali leaching processes, respectively. Utilizing carbide slag to replace the energy-intensive NaOH for pH adjustment in the leaching solution resulted in a Ca2+ concentration of 21,922 mg/L in the filtrate after co-precipitation. Through further mineralization process, CO2 sequestration was achieved alongside the production of CaCO3 with the content reaching 98.5 % along with a whiteness of 94.4 %. Furthermore, by adjusting the experimental parameters in the mineralization process, controlled manipulation of the phase and morphology of the CaCO3 product could be achieved to meet various industry requirements. To summarize, the complete resource recovery of red mud and carbide slag was achieved in this study, demonstrating the promising potential in practical applications.

Effect of pH on hydroxyapatite coatings obtained by spray pyrolysis and their use as matrices for antibiotic adsorption by spin coating and release properties.

Calcium phosphate materials, particularly hydroxyapatite (HA), are extensively used in biomedical applications because of their prominence as primary inorganic constituents of human hard tissues. This study investigates the synthesis of HA coatings via spray pyrolysis using various precursors, including HA derived from bovine bone. The effects of pH on the formation and properties of HA coatings were systematically examined. Samples exposed to acidic conditions or left without pH adjustment led to the formation of HA, contrasting with the outcomes observed through dissolution methods. Different characterization techniques, such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD), were employed to evaluate the quality and crystallinity of the coatings. Among the samples, those exhibiting superior crystallinity and nanostructured features, including bovine HA, were selected for further surface functionalization with the antibiotic enrofloxacin using spin coating. As expected, the antibiotic loading on each material's surface depended on the amount of HA deposited on the substrate. However, the desorption results indicated that, in all cases, desorption persisted beyond 38 h, implying that HA-loaded matrices could be effective systems for controlled and prolonged drug release, which could be useful in dental or orthopedic implants for inhibiting the growth of bacterial biofilms.

Overlooked pyrite-mediated heterogeneous Fenton processes: Mechanisms of surface hydroxyl radical generation and associated decontamination performance

Pyrite-based Fenton-like processes have been extensively studied for wastewater decontamination; however, most relevant studies placed excessive emphasis on the homogeneous Fenton reaction mediated by aqueous Fe2+, resulting in the proposed technologies facing issues such as additional acid requirements for pH adjustment and excessive iron sludge production. Herein, through in situ shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS), custom dual-chamber reactor experiments, and a series of control experiments, significant hydroxyl radical generation was identified during the pyrite/H2O2 process, while the dominant reactive iron species was verified to the structural Fe sites on the pyrite surface, rather than structural Fe(II) in secondary iron minerals and surface adsorbed Fe2+. Consequently, even with significant suppression of the homogeneous Fenton pathway, the pyrite/H2O2 process exhibited significant degradation efficiency for sulfamethoxazole (SMX) at pH 4. Moreover, the pyrite/H2O2 process was found to selectively remove 50 μM of pollutants with high affinity for pyrite (bisphenol A, carbamazepine, nitrobenzene, and SMX), even in the presence of 50–100 mM methanol. Compared to the typical iron-based reductive catalyst (zero-valent iron, ZVI), pyrite mediated a Fenton process with greater potential for practical applications at pH 4, achieving a 43.75-fold reduction in iron sludge production and almost doubling the H2O2 utilization efficiency. Additionally, in contrast to ZVI, minimal iron oxide formed on the pyrite surface during the oxidation process. Thus, after seven cycles of degradation experiments, the decontamination efficiency of the pyrite/H2O2 process remained stable. These findings are crucial for understanding the complex environmental behavior of pyrite in both natural and engineering processes and provide a new perspective for the efficient utilization of pyrite resources as well.

Research progress on plant‐based glue in meat substitutes: main components, formation mechanisms, challenges, and development

SummaryThe growing recognition of environmental conservation and human well‐being has led to a surge in the advancement of plant‐based meat. These meat alternatives are similar to animal meat products regarding texture, flavour, shape, and other characteristics. These products consist of three main components: plant tissue proteins, fat mimetics, and plant‐based glues that act as binders. Since meat substitutes are subjected to high temperatures and pressures or refrigeration, the junction between the tissue proteins and fat mimetics is prone to cracking, necessitating the development of adhesives with excellent bonding characteristics. The physicochemical properties and functional applications of plant glues are currently attracting significant research attention. Plant‐based glues are essentially gels derived from substances such as proteins, polysaccharides, or various compounds. This article summarised the basic principles of gel formation, focusing on acid‐, salt‐, heat‐, and enzyme‐induced gel formation pathways, as well as the role of pH adjustment and enzyme or salt ion addition in improving their functional properties. Optimal conditions can enhance the adhesive properties of plant‐based glues. This article reviewed the types, gelation mechanisms, influencing factors, and challenges of plant‐based glues to provide a theoretical basis for research on their application potential.

Reagent-free phosphorus precipitation from a denitrified swine effluent in a batch electrochemical system

There is high interest in the recovery of phosphorus (P) from wastewater through crystallization processes. However, the addition of chemical reagents (e.g., sodium hydroxide) to raise the pH may result in high treatment costs and increased concentrations of undesired metal ions (e.g., sodium). As an alternative, in this research we considered electrochemical mediated precipitation at low current densities (0.4–1.2 A m−2) without using chemical reagents. For that purpose, a two-chamber electrochemical system was operated in batch for treating denitrified swine effluent (48 mg P L−1). By applying current at 1.2 A m−2, and targeting pH 11.5, a maximum P removal rate of 33.4 mmol P (L·d−1) was obtained while the P removal efficiency was above 90 %. New solids that formed mostly remained suspended in the catholyte. Before discharge, the catholyte effluent was recirculated to the anodic compartment to neutralize the pH, achieving a final pH of 6.4 ± 0.1. Chlorine (Cl2) production in the anodic compartment was favored by a small anode surface and a high initial pH of the catholyte. Although the production of chlorine achieved was limited (the highest concentration was 8.6 ± 0.1 mg Cl2 L−1) these findings represent a new opportunity for the recovery and onsite use of this side-product. Electrochemical impedance spectroscopy tests confirmed that the deposition of solids inside the cathodic compartment during the experimental period was limited. Membrane analysis revealed significant scaling of carbonate compounds. The electrochemical treatment described above was shown as a promising alternative to sodium hydroxide and sulfuric acid dosage for pH adjustment when crystallizing phosphate salts.

Tailoring the luminescent and structural behaviors of pH-driven PPy/gC3N4/ZrO2 nanocomposite as an emissive layer material for OLED application

The polymeric nanocomposites were synthesized via an in-situ polymerization method, optimized through pH adjustment of zirconium oxide rather than concentration variation. X-ray powder diffraction analysis revealed phase transitions and average crystallite sizes ranging from approximately 6.52–9.16 nm, depending on the pH levels. Field Emission Scanning Electron Microscopy tool is used to analyze the granular nanosheets and nanoparticles like the microstructure of polypyrrole, graphitic carbon nitride and zirconium oxide at a high resolution. UV–visible spectroscopy determined an optical bandgap energy of about 2.44 eV, a refractive index of 2.17, and an optical conductivity of 3.15 × 1010 S/cm2. Forster resonance energy transfer between Zirconium dioxide and graphitic carbon nitride significantly enhanced photoluminescence emission. PL emission and color purity (45 %) of the optimized sample were examined using photoluminescence data. Electrical conductivity of ∼15.9 × 10−4 S/cm and dielectric constant of ∼14.77 were obtained from I to V and LCR meter measurements. These properties indicate that the pH-driven nanocomposite exhibits optimized electron-hole recombination rates, electrical conductivity, and suitable bandgap energy, making its potential impact as an emissive layer material for OLED applications.