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Prevention of hydrate plugs during transportation of oil and natural gas in the pipeline network is challenging. Certain additives are often introduced into the process to eliminate/delay plug formation. Dominantly synthetic inhibitors are deployed in large volumes (∼20 to 30% by volume) to counter the problem and are highly expensive and, in some circumstances, toxic. The search for novel additives that are eco-friendly and act as inhibitors is in demand. The present study reports the thermodynamic inhibition (THI) capacity of some vastly available natural biopowders, such as (neem), (betel), and (Indian lotus) in low dosage (0.5 wt %), on methane hydrate (MH) formation. Since the gas flow is dynamic, experiments are conducted in stirred geometry by varying the speed range from 0 to 1000 rotations per minute (rpm). All of the studies are performed in the isochoric method procedure. The biopowders act as efficient thermodynamic hydrate inhibitors. Once the nucleation triggers, they act as kinetic hydrate promoters. Since sodium dodecyl sulfate (SDS) is an excellent kinetic hydrate promoter in both stirred and nonstirred geometries, the obtained results are compared with the SDS system. Hydrate nucleation is triggered at higher subcooling (∼8 to 10 K) in the presence of water-soluble bioextracts. The neem leaf extracts showed a ∼30% lower hydrate conversion than SDS in identical experimental conditions. Two-stage hydrate nucleation occurred at higher stirring speeds, and the hydrate conversion is inferior (∼6%) between the primary and secondary stages. The addition of biopowder extracts is useful in controlling hydrate formation. A small quantity of biopowders provides higher inhibition and reduces synthetic chemicals used in real-time applications.
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http://dx.doi.org/10.1021/acsomega.0c06328 | DOI Listing |
J Phys Chem B
September 2025
Key Laboratory of Physics and Technology for Advanced Batteries, College of Physics, Jilin University, Changchun 130012, China.
Understanding hydrogen bonding and ion-specific interactions in water, sodium sulfate (NaSO), and acetonitrile (ACN) systems remains challenging due to their complex, dynamic nature. Here, Raman spectroscopy is employed to probe hydrogen bonding networks and ion reorganization in NaSO aqueous solutions with different ACN concentrations. The results indicate that, at low ACN concentrations in the ternary solutions, hydrogen bonding between ACN and water molecules disrupts the original hydration structure of the ions, resulting in the formation of small ion clusters via electrostatic interactions.
View Article and Find Full Text PDFBiomed Mater
September 2025
Department of Nanobiotechnology, Faculty of Biological Sciences, , Tarbiat Modares University, Tehran, P.O. Box 14115-154, Iran, Tehran, Tehran Province, 14115-154, Iran (the Islamic Republic of).
It is essential to develop new strategies for wound treatment and skin reconstruction, particularly by scaffolds that replicate the structure and function of native skin. A bilayer scaffold was developed using three-dimensional (3D) bioprinting, based on a uniform chitosan-based formulation for both layers, maintaining material uniformity while offering structural support and promoting cell adhesion. The upper chitosan layer, embedded with NHEK-Neo, is stiffer and mimics the epidermis, while the softer lower layer contains embedded HFFs and HFSCs, mimicking the dermis.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
School of Chemistry, Dalian University of Technology, Dalian 116024, PR China; College of Environment and Chemical Engineering, Dalian University, Dalian 116622, China. Electronic address:
Aqueous batteries have become a prospective future energy storage system because of their low coefficient of cost and stability. However, their lower energy density limits their applications. Ammonium ions (NH) have a small hydration radius and light molar mass, and aqueous ammonium ion batteries (AAIBs) are anticipated for solving the inherent low-energy density problem of aqueous batteries.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Research Centre of Ecology & Environment for Coastal Area and Deep Sea, Guangdong University of Technology, Guangzhou 510006, China; Guangdong Basic Research Center of Excellence for Ecological Security and Green Development, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou),
Hypothesis: Gas hydrate formation in sediments is influenced by the availability of gas-water interfacial areas, which governs gas-water interactions. The surface wettability of sediment particles is expected to affect the spatial distribution of water within the pore space, thereby altering the extent of gas-liquid contact. Consequently, by tuning the wettability heterogeneity of the sediment, the spatial distribution of pore water can be regulated, which in turn influences the gas-water interactions and the kinetics of gas hydrate formation.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
The Steve Sanghi College of Engineering, Mechanical Engineering, Northern Arizona University, Flagstaff, Arizona 86011, United States.
This study investigates the HO and CO sorption behavior of two chemically distinct polystyrene-divinylbenzene-based ion exchange sorbents: a primary amine and a permanently charged strong base quaternary ammonium (QA) group with (bi)carbonate counter anions. We compare their distinct interactions with HO and CO through simultaneous thermal gravimetric, calorimetric, gas analysis, and molecular modeling approaches to evaluate their performance for dilute CO separations like direct air capture. Thermal and hybrid (heat + low-temperature hydration) desorption experiments demonstrate that the QA-based sorbent binds both water and CO more strongly than the amine counterparts but undergoes degradation at moderate temperatures, limiting its compatibility with thermal swing regeneration.
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