Investigating mixed biosolids and cardboard for methylene blue adsorption: Activation, adsorption modelling and thermodynamics.

Ongoing global population boom has led to the rise in waste and related research on increasing its economic value. In such an attempt, this study aims to activate gas-to-liquids (GTL) derived biosolids (BS) and cardboard (CB) and mixed samples (50:50) using potassium carbonate to produce three activated carbons (ACs): KBS, KCB and KM respectively. The characterization of the samples revealed surface areas of 156, 515, and 527 m2/g for KBS, KCB, and KM, respectively based on Brunauer-Emmett-Teller (BET) analysis, with increased porosity and metal content after activation evident from the Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS) results, as well as the presence of magnetite in the KBS and KM samples apparent from the X-ray powder diffraction (XRD) results. Additionally, Fourier Transform Infrared Spectroscopy (FTIR) results indicate increased C-O-C stretches and O-H bonds after activation of the samples. The ACs were used for methylene blue (MB) removal process which is a rapid for all three samples, reaching equilibrium after 9 h, and optimal at neutral pH and maximum at the highest temperature, 40 °C. The MB adsorption capacity was highest for KM (191.07 mg/g), followed by the KCB and KBS samples. Isotherm modelling of the samples showed best fits for KBS, KCB and KM as Langmuir-Freundlich (LF), Langmuir and Toth models respectively. On the contrary, kinetic modelling using contact time study data for all samples exhibited best fits by the Diffusion-chemisorption (DC) model. Finally, the thermodynamic calculations of the mixed sample disclosed the adsorption process to be exothermic and spontaneous, with potential mechanisms being electrostatic attraction, ion exchange, π-π interactions, and hydrogen bonding. Multiple cycles of KM regeneration was also achieved with good adsorption capacities. Future work will explore other activation methods and examine the magnetic properties of KBS and KM for real water treatment.

Sustainable Solution for Plastic Pollution: Upcycling Waste Polypropylene Masks for Effective Oil-Spill Management.

The use of Polypropylene PP in disposable items such as face masks, gloves, and personal protective equipment has increased exponentially during and after the COVID-19 pandemic, contributing significantly to microplastics and nanoplastics in the environment. Upcycling of waste PP provides a useful alternative to traditional thermal and mechanical recycling techniques. It transforms waste PP into useful products, minimizing its impact on the environment. Herein, we synthesized an oil-sorbent pouch using waste PP, which comprises superposed microporous and fibrous thin films of PP using spin coating. The pouch exhibited super-fast uptake kinetics and reached its saturation in fewer than five minutes with a high oil uptake value of 85 g/g. Moreover, it displayed high reusability and was found to be effective in absorbing oil up to seven times when mechanically squeezed between each cycle, demonstrating robust oil-sorption capabilities. This approach offers a potential solution for managing plastic waste while promoting a circular economy.

Adsorption of Methyl Orange from Water Using Chitosan Bead-like Materials.

Natural product waste treatment and the removal of harmful dyes from water by adsorption are two of the crucial environmental issues at present. Traditional adsorbents are often not capable in removing detrimental dyes from wastewater due to their hydrophilic nature and because they form strong bonds with water molecules, and therefore they remain in the dissolved state in water. Consequently, new and effective sorbents are required to reduce the cost of wastewater treatment as well as to mitigate the health problems caused by water pollution contaminants. In this study, the adsorption behaviour of methyl orange, MO, dye on chitosan bead-like materials was investigated as a function of shaking time, contact time, adsorbent dosage, initial MO concentration, temperature and solution pH. The structural and chemical properties of chitosan bead-like materials were studied using several techniques including SEM, BET, XRD and FTIR. The adsorption process of methyl orange by chitosan bead materials was well described by the Langmuir isotherm model for the uptake capacity and followed by the pseudo-second-order kinetic model to describe the rate processes. Under the optimal conditions, the maximum removal rate (98.9%) and adsorption capacity (12.46 mg/g) of chitosan bead-like materials were higher than those of other previous reports; their removal rate for methyl orange was still up to 87.2% after three regenerative cycles. Hence, this chitosan bead-like materials are very promising materials for wastewater treatment.

A Review on Catalytic Fast Co-Pyrolysis Using Analytical Py-GC/MS.

Py-GC/MS combines pyrolysis with analytical tools of gas chromatography (GC) and mass spectrometry (MS) and is a quick and highly effective method to analyse the volatiles generated from small amounts of feeds. The review focuses on using zeolites and other catalysts in the fast co-pyrolysis of various feedstocks, including biomass wastes (plants and animals) and municipal waste materials, to improve the yield of specific volatile products. The utilisation of zeolite catalysts, including HZSM-5 and nMFI, results in a synergistic reduction of oxygen and an increase in the hydrocarbon content of pyrolysis products. The literature works also indicate HZSM-5 produced the most bio-oil and had the least coke deposition among the zeolites tested. Other catalysts, such as metals and metal oxides, and feedstocks that act as catalysts (self-catalysis), such as red mud and oil shale, are also discussed in the review. Combining catalysts, such as metal oxides and HZSM-5, further improves the yields of aromatics during co-pyrolysis. The review highlights the need for further research on the kinetics of the processes, optimisation of feed-to-catalyst ratios, and stability of catalysts and products.

Removal of Methylene Blue from Water Using Magnetic GTL-Derived Biosolids: Study of Adsorption Isotherms and Kinetic Models.

Global waste production is significantly rising with the increase in population. Efforts are being made to utilize waste in meaningful ways and increase its economic value. This research makes one such effort by utilizing gas-to-liquid (GTL)-derived biosolids, a significant waste produced from the wastewater treatment process. To understand the surface properties, the biosolid waste (BS) that is activated directly using potassium carbonate, labelled as KBS, has been characterized using scanning electron microscopy and energy dispersive X-ray spectroscopy (SEM-EDS), X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD), and Brunauer-Emmett-Teller (BET). The characterization shows that the surface area of BS increased from 0.010 to 156 m2/g upon activation. The EDS and XPS results show an increase in the metal content after activation (especially iron); additionally, XRD revealed the presence of magnetite and potassium iron oxide upon activation. Furthermore, the magnetic field was recorded to be 0.1 mT using a tesla meter. The magnetic properties present in the activated carbon show potential for pollutant removal. Adsorption studies of methylene blue using KBS show a maximum adsorption capacity of 59.27 mg/g; the adsorption process is rapid and reaches equilibrium after 9 h. Modelling using seven different isotherm and kinetic models reveals the best fit for the Langmuir-Freundlich and Diffusion-chemisorptionmodels, respectively. Additional thermodynamic calculations conclude the adsorption system to be exothermic, spontaneous, and favoring physisorption.

A novel approach on the delineation of a multipurpose energy-greenbelt to produce biofuel and combat desertification in arid regions.

Jatropha curcas L. (JCL) is one of the most prominent energy crops due to its superior agronomical traits, where it can grow in non-arable lands and harsh climates with minimal water requirements. A significant number of studies were published on the utilisation of JCL for biofuel production, whereas there are no studies on its use in greenbelt (GB) or windbreak technologies reported thus far. Meanwhile, a few approaches on the delineation of greenbelts to fight desertification in the arid regions exist in literature. This study presents a novel approach to delineate a multipurpose energy-greenbelt using JCL crop for biofuel production, as well as to preserve the soil and enhance air quality, thereby helping to combat desertification and sand-dust storms (SDS). The methodology is demonstrated using a case study in the state of Qatar for the diversification of its renewable energy resources. Moreover, Qatar is also suffering from land degradation due to erosion factors and desert creep. A multi-dimensional approach is proposed for this purpose using satellite and meteorological data to initially select the optimal plantation sites that potentially contribute to the highest possible biofuel yield. The spatial analysis was carried out using the analytical hierarchy process (AHP) technique for multi-criteria decision making in the geographic information system (ArcGIS). In addition, the Landsat and MODIS satellite imagery were utilised in combination with historical records from the weather stations to evaluate the patterns of SDS, land degradation and urban expansion, to best define optimal GB pathway. COMSOL Multiphysics software was subsequently employed to evaluate the performance of Jatropha-GB and determine its optimal density. The different solutions for GB delineation spans 166.6-227.8 km length and (6 × 6 m) of field density. It is expected that the economic and environmental benefits from the derived GB configuration include: (a) protection of up to 87% of Qatar farms against further deterioration; (b) yield of up to 36 M gallon of green liquid fuels; (c) capture of 0.33 M tonnes of CO2 per 1 km GB-depth annually; and (d) provide a better air quality for around 95% of the Qatar population.

Layered Double Hydroxides as Rising-Star Adsorbents for Water Purification: A Brief Discussion.

Within the frame of this article, briefly but comprehensively, we present the existing knowledge, perspectives, and challenges for the utilization of Layered Double Hydroxides (LDHs) as adsorbents against a plethora of pollutants in aquatic matrixes. The use of LDHs as adsorbents was established by considering their significant physicochemical features, including their textural, structural, morphological, and chemical composition, as well as their method of synthesis, followed by their advantages and disadvantages as remediation media. The utilization of LDHs towards the adsorptive removal of dyes, metals, oxyanions, and emerging pollutants is critically reviewed, while all the reported kinds of interactions that gather the removal are collectively presented. Finally, future perspectives on the topic are discussed. It is expected that this discussion will encourage researchers in the area to seek new ideas for the design, development, and applications of novel LDHs-based nanomaterials as selective adsorbents, and hence to further explore the potential of their utilization also for analytic approaches to detect and monitor various pollutants.

Thermal degradation characteristics and gasification kinetics of camel manure using thermogravimetric analysis.

In this work, the sustainable valorisation of camel manure has been studied using thermogravimetric analysis. The gasification tests were performed from ambient conditions to 950 °C at 10, 20, and 50 °C/min under an O2 environment. The TGA data were applied to determine the kinetics of the O2 gasification. Single-heating rate models (Arrhenius and Coats-Redfern) and multi-heating rate models (Distributed activation energy, Friedman, Flynn-Wall-Ozawa, Starink, and Kissinger-Akahira-Sunose) were applied to estimate the kinetics of the process. Between the two single-heating rate models, the Coats-Redfern method fitted best with the experimental data. Among the multi-heating rate models, the Flynn-Wall-Ozawa model fitted best with the experimental results. The kinetic parameters-frequency factor, activation energy, and order of reaction were estimated using the Flynn-Wall-Ozawa model (the best-fitting model) and the estimated kinetic parameters were used to calculate the thermodynamic properties-Gibbs free energy, enthalpy, and entropy. The information on these kinetic and thermodynamic properties can be useful for the design of gasifiers and for optimising the O2 gasification operating conditions.

Review of phosphate removal from water by carbonaceous sorbents.

In the last decades, phosphate is considered the main cause of eutrophication and has received substantial attention from the scientific community. Phosphate is a major pollutant that deteriorates water quality, which has been increasing in water resources, primarily due to the increasing global population and corresponding activities. Adsorption technology is amongst the different technologies used to decrease the phosphate levels in water, and has been found to be highly effective even at low phosphate concentrations. Carbonaceous materials and their composites have been widely used for phosphate removal due to their exceptional surface properties and high phosphate sorption capacity. Considering the importance of the topic, this study reviews the reported literature in the field of adsorptive removal of phosphate over various carbon-based adsorbents such as activated carbon, charcoal, graphene, graphene oxide, graphite and carbon nanotubes. Moreover, insights into the adsorption behaviour, experimental parameters, mechanisms, thermodynamics, effect of coexisting ions and the possible desorption processes of phosphate onto modified and unmodified carbonaceous adsorbents are also considered. Finally, research challenges and gaps have been highlighted.

Utilization of MWCNTs/Al2O3 as adsorbent for ciprofloxacin removal: equilibrium, kinetics and thermodynamic studies.

In the present study, the adsorption behavior of ciprofloxacin (CIP) from aqueous solution onto MWCNTs/Al2O3 was studied using batch experiments. Physical characterization of MWCNTs/Al2O3 was determined by SEM, XRD, and BET. The effective parameters investigated included: initial CIP concentration, contact time, MWCNTs/Al2O3 mass, and temperature. Based on experimental results and correlation coefficients, the rate of CIP adsorption followed the pseudo-second-model kinetics. Complete compatibility of the adsorption isotherm process was achieved with the Langmuir model, and the maximum adsorption capacity reached 41.73 mg/g under the optimized conditions (pH = 7, MWCNTs/Al2O3 dose = 1.2 g/L, contact time = 60 min, initial concentration = 10 mg/L, and temperature= 45 °C). The adsorption capacities based on the Langmuir model at different temperatures, 273, 288, 303, and 318 K, were equal to 72.18, 75.92, 79.65, and 83.47 mg/g, respectively. The determined parameters of the thermodynamic studies demonstrated the endothermic and spontaneous nature of the biosorption. The mean free energy was estimated from D-R isotherm model to be 0.316-0.707 KJ/mol, which clearly proved that the adsorption experiment followed a physical process. The data suggest that MWCNTs/Al2O3 could be used as a highly effective adsorbent material with a high capacity for the removal of antibiotics from water and wastewater.

Kinetic and thermodynamic investigations of surfactants adsorption from water by carbide-derived carbon.

The objective of the study is to investigate the potential of carbide-derived carbon (CDC) for the adsorptive removal of nonionic t-octylphenoxy poly ethoxy ethanol (TX-100), anionic sodium dodecylbenzene sulfonate (SDBS) and cationic 1-hexadecylpyridinium bromide (HDPB) surfactants from water. The CDC was characterized using TEM, SEM, FTIR, BET, EDS, XPS methods and zeta potential measurements. The effects of adsorption parameters included initial surfactant concentration, contact time, temperature, and pH of the feed solution were evaluated. The adsorption capacity and mechanism were determined by modeling the isotherm, kinetic and thermodynamic data. The kinetics results demonstrated that the adsorption of the surfactant by CDC obeys the pseudo 2nd order model. The thermodynamic results have shown that surfactants adsorption by CDC is an endothermic and spontaneous process. The Sips model agreed with the adsorption isotherm data of SDBS with R2 of 0.987, while both Freundlich and Redlich-Peterson models comply well with adsorption data for TX-100 and HDPB. The hydrophobic and electrostatic interactions were found the dominant mechanisms of the adsorption of the surfactant by CDC. The adsorption capacities of CDC were found to be 442.4, 462.0 and 578.4 mg/g for SDBS, HDPB and TX-100, respectively.

The impact of pyrolysis conditions on orange peel biochar physicochemical properties for sandy soil.

The citrus industry is considered one of the main contributors to agricultural waste. Peels are commonly used in the food industry or as feedstock in biorefining. In this study, the potential of waste orange peel biochar for agricultural applications in sandy soil was investigated. This will not only increase the percentage of agricultural waste recycling, but also lead to more sustainable agriculture with environmental benefits such as carbon sequestration. Biochar was produced through slow pyrolysis in the temperature range 300-600°C and at two holding durations (10 min and 60 min). Both factors had a significant impact on the physicochemical characteristics of biochar in the heating region 300-450°C. However, varying the holding time for pyrolysis temperatures beyond 450°C had a diminishing effect on biochar properties compared with the impact of increasing pyrolysis temperature. The study also looked at certain properties that are specific to agricultural application not previously reported for orange peel. Very high cation exchange capacities of 70 cmol kg-1 were achieved at 300°C, whereas water holding capacity was not strongly influenced by pyrolysis conditions. Preliminary planting tests indicate potential for improving agricultural sustainability in sandy soils. The technoeconomic analysis of biochar showed that the pyrolysis process can be profitable with sufficient plant capacity.

Application of cadmium-doped ZnO for the solar photocatalytic degradation of phenol.

In this study, photocatalysis of phenol was studied using Cd-ZnO nanorods, which were synthesized by a hydrothermal method. The Cd-ZnO photocatalyst was characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy, and Fourier transform infrared (FT-IR) and UV-Vis spectroscopy. XRD patterns exhibit diffraction peaks indexed to the hexagonal wurtzite structures with the P63mc space group. SEM images showed that the average size of the Cd-ZnO nanorods was about 90 nm. Moreover, the nanorods were not agglomerated and were well-dispersed in the aqueous medium. FT-IR analysis confirmed that a surface modifier (n-butylamine) did not add any functional groups onto the Cd-ZnO nanorods. The dopant used in this study showed reduction of the bandgap energy between valence and conduction of the photocatalyst. In addition, effect of various operational parameters including type of photocatalyst, pH, initial concentration of phenol, amount of photocatalyst, and irradiation time on the photocatalytic degradation of phenol has been investigated. The highest phenol removal was achieved using 1% Cd-ZnO for 20 mg/l phenol at pH 7, 3 g/l photocatalyst, 120 min contact time, and 0.01 mole H2O2.

Multilayer Dye Adsorption in Activated Carbons-Facile Approach to Exploit Vacant Sites and Interlayer Charge Interaction.

Altering the textural properties of activated carbons (ACs) via physicochemical techniques to increase their specific surface area and/or to manipulate their pore size is a common practice to enhance their adsorption capacity. Instead, this study proposes the utilization of the vacant sites remaining unoccupied after dye uptake saturation by removing the steric hindrance and same-charge repulsion phenomena via multilayer adsorption. Herein, it has been shown that the adsorption capacity of the fresh AC is a direct function of the dye molecular size. As the cross-sectional area of the dye molecule increases, the steric hindrance effect exerted on the neighboring adsorbed molecules increases, and the geometrical packing efficiency is constrained. Thus, ACs saturated with larger dye molecules render higher concentrations of vacant adsorption sites which can accommodate an additional layer of dye molecules on the exhausted adsorbent through interlayer attractive forces. The second layer adsorption capacity (60-200 mg·g(-1)) has been demonstrated to have a linear relationship with the uncovered surface area of the exhausted AC, which is, in turn, inversely proportional to the adsorbate molecular size. Unlike the second layer adsorption, the third layer adsorption is a direct function of the charge density of the second layer.

Sustainable development of tyre char-based activated carbons with different textural properties for value-added applications.

This paper aims at the sustainable development of activated carbons for value-added applications from the waste tyre pyrolysis product, tyre char, in order to make pyrolysis economically favorable. Two activation process parameters, activation temperature (900, 925, 950 and 975 °C) and residence time (2, 4 and 6 h) with steam as the activating agent have been investigated. The textural properties of the produced tyre char activated carbons have been characterized by nitrogen adsorption-desorption experiments at -196 °C. The activation process has resulted in the production of mesoporous activated carbons confirmed by the existence of hysteresis loops in the N2 adsorption-desorption curves and the pore size distribution curves obtained from BJH method. The BET surface area, total pore volume and mesopore volume of the activated carbons from tyre char have been improved to 732 m(2)/g, 0.91 cm(3)/g and 0.89 cm(3)/g, respectively. It has been observed that the BET surface area, mesopore volume and total pore volume increased linearly with burnoff during activation in the range of experimental parameters studied. Thus, yield-normalized surface area, defined as the surface area of the activated carbon per gram of the precursor, has been introduced to optimize the activation conditions. Accordingly, the optimized activation conditions have been demonstrated as an activation temperature of 975 °C and an activation time of 4 h.

Aluminosilicate-based adsorbent in equimolar and non-equimolar binary-component heavy metal removal systems.

Cadmium (Cd) and lead (Pb) are toxic heavy metals commonly used in various industries. The simultaneous presence of these metals in wastewater amplifies the toxicity of wastewater and the complexity of the treatment process. This study has investigated the selective behavior of an aluminosilicate-based mesoporous adsorbent. It has been demonstrated that when equimolar quantities of the metals are present in wastewater, the adsorbent uptakes the Pb²âº ions selectively. This has been attributed to the higher electronegativity value of Pb²âº compared to Cd²âº which can be more readily adsorbed on the adsorbent surface, displacing the Cd²âº ions. The selectivity can be advantageous when the objective is the separation and reuse of the metals besides wastewater treatment. In non-equimolar solutions, a complete selectivity can be observed up to a threshold Pb²âº molar ratio of 30%. Below this threshold value, the Cd²âº and Pb²âº ions are uptaken simultaneously due to the abundance of Cd²âº ions and the availability of adsorption sites at very low Pb²âº molar ratios. Moreover, the total adsorption capacities of the adsorbent for the multi-component system have been shown to be in the same range as the single-component system for each metal ion which can be of high value for industrial applications.

Transforming polypropylene waste into transparent anti-corrosion weather-resistant and anti-bacterial superhydrophobic films.

The global pollution crisis arising from the accumulation of plastic in landfills and the environment necessitates addressing plastic waste issues. Notably, polypropylene (PP) waste accounts for 20% of total plastic waste and holds promise for hydrophobic applications in the realm of recycling. Herein, the transparent and non-transparent superhydrophobic films made from waste PP are reported. A hierarchical structure with protrusions is induced through spin-casting and thermally induced phase separation. The films had a water contact angle of 159° and could vary in thickness, strength, roughness, and hydrophobicity depending on end-user requirements. The Bode plot indicated enhanced corrosion resistance in the superhydrophobic films. Antibacterial trials with Escherichia coli and Staphylococcus aureus microbial solutions showed that the superhydrophobic film had a significantly lower rate of colony-forming units compared to both the transparent surface and the control blank sample. Moreover, a life cycle assessment revealed that the film production resulted in a 62% lower embodied energy and 34% lower carbon footprint compared to virgin PP pellets sourced from petroleum. These films exhibit distinctiveness with their dual functionality as coatings and freestanding films. Unlike conventional coatings that require chemical application onto the substrate, these films can be mechanically applied using adhesive tapes on a variety of surfaces. Overall, the effective recycling of waste PP into versatile superhydrophobic films not only reduces environmental impact but also paves the way for a more sustainable and eco-friendly future.

Prolonged Lifespan of Superhydrophobic Thin Films and Coatings Using Recycled Polyethylene.

High-density polyethylene (HDPE) waste poses a significant environmental challenge due to its non-biodegradable nature and the vast quantities generated annually. However, conventional recycling methods are energy-intensive and often yield low-quality products. Herein, HDPE waste is upcycled into anti-aging, superhydrophobic thin films suitable for outdoor applications. A two-layer spin-casting method combined with heating-induced crosslinking is utilized to produce an exceptionally rough superhydrophobic surface, featuring a root mean square (RMS) roughness of 50 nm, an average crest height of 222 nm, an average trough depth of -264 nm, and a contact angle (CA) of 148°. To assess durability, weathering tests were conducted, revealing the films' susceptibility to degradation under harsh conditions. The films' resistance to environmental factors is improved by incorporating a UV absorber, maintaining their hydrophobic properties and mechanical strength. Our research demonstrates a sustainable method for upcycling waste into high-performance, weather-resistant, superhydrophobic films.

Techno-economic and environmental analyses of the pyrolysis of food waste to produce bio-products.

Food waste has become a source of concern as it is generated abundantly worldwide and needs to be valorised into new products. In this study, cucumber, tomato, and carrot wastes were investigated as pyrolysis feedstocks as a single component (cucumber), a binary component mixture (cucumber and tomato), and a ternary component blend (cucumber, tomato, and carrot). Fourteen scenarios were simulated and evaluated based on varying the feedstock blend (single, binary, and tertiary), temperature (300 and 500 °C), and feedstock moisture content (5, 20, and 40%). Using an established empirical model, the effect of these parameters on product yields, techno-economic implications, energy requirements, and life cycle analysis (LCA) outcomes were investigated. The best performers of each scenario were determined, and their strengths and weaknesses were identified and compared with other scenarios. In terms of product yields, all three systems (single, binary, and tertiary) followed a similar pattern: bio-oil yields increased as temperature and feedstock moisture content increased, while biochar yields decreased as temperature and feedstock moisture content increased. The production of syngas, on the other hand, was only observed at elevated temperatures. The total energy requirement exhibited an increase with increasing temperature and feedstock moisture content. The economic evaluation revealed that the return on investment (ROI) value for the single component at 5% moisture content at 300 °C is 29%, with a payback period (PB) of only 3.4 years, which is potentially very appealing. The water footprint increased with increasing pyrolysis temperature but decreased with increasing moisture content in all scenarios. The land footprint is observed to remain constant despite changes in process conditions. The study's findings contribute to the pyrolysis process's scalability, technological advancement, and commercialisation.

Evaluation of cell disruption methods for protein and coenzyme Q10 quantification in purple non-sulfur bacteria.

A recent focus has been on the recovery of single-cell protein and other nutritionally valuable bioproducts, such as Coenzyme Q10 (CoQ10) from purple non-sulfur bacteria (PNSB) biomass following wastewater treatment. However, due to PNSB's peculiar cell envelope (e.g., increased membrane cross-section for energy transduction) and relatively smaller cell size compared to well-studied microbial protein sources like yeast and microalgae, the effectiveness of common cell disruption methods for protein quantification from PNSB may differ. Thus, this study examines the efficiency of selected chemical (NaOH and EDTA), mechanical (homogenization and bead milling), physical (thermal and bath/probe sonication), and combined chemical-mechanical/physical treatment techniques on the PNSB cell lysis. PNSB biomass was recovered from the treatment of gas-to-liquid process water. Biomass protein and CoQ10 contents were quantified based on extraction efficiency. Considering single-treatment techniques, bead milling resulted in the best protein yields (p < 0.001), with the other techniques resulting in poor yields. However, the NaOH-assisted sonication (combined chemical/physical treatment technique) resulted in similar protein recovery (p = 1.00) with bead milling, with the former having a better amino acid profile. For example, close to 50% of the amino acids, such as sensitive ones like tryptophan, threonine, cystine, and methionine, were detected in higher concentrations in NaOH-assisted sonication (>10% relative difference) compared to bead-milling due to its less disruptive nature and improved solubility of amino acids in alkaline conditions. Overall, PNSB required more intensive protein extraction techniques than were reported to be effective on other single-cell organisms. NaOH was the preferred chemical for chemical-aided mechanical/physical extraction as EDTA was observed to interfere with the Lowry protein kit, resulting in significantly lower concentrations. However, EDTA was the preferred chemical agent for CoQ10 extraction and quantification. CoQ10 extraction efficiency was also suspected to be adversely influenced by pH and temperature.