Colloid Science Research Articles

Adsorption Behavior of Fluorocarbon Surfactants on Polytetrafluoroethylene Surface

By using the sessile drop method, the wetting properties of nonionic fluorocarbon surfactants (FNS-1 and FNS-2) and anionic fluorocarbon surfactant (FAS) solutions on the surface of polytetrafluoroethylene (PTFE) were investigated. Meanwhile, the effects of surfactant concentration on the contact angle, adhesion tension, PTFE–liquid interfacial tension, and work of adhesion of the fluorocarbon surfactant with different structures were detected. The results demonstrate that the adsorption amount of the three fluorocarbon surfactants at the air–liquid interface is 1.5~2 times higher than their adsorption amount at the PTFE–solution interface. Before critical micelle concentration (CMC), the fluorocarbon surfactant molecules rely on their hydrophobic groups to adsorb on the PTFE surface. The smallest molecular size of FNS-2 results in the largest adsorption amount, while electrostatic repulsion and large steric hindrance result in the smallest adsorption amount for FAS. Above CMC, the fluorocarbon surfactants form semi-micelles to adsorb on the PTFE surface. The hydrophilic modification ability of the three fluorocarbon surfactants for the PTFE surface is stronger than that of reported surfactants, and the contact angle can be reduced to about 20° at high concentrations. The order of the hydrophilic modification ability is FNS-2 > FNS-1 > FAS. Hydrophilic EO groups can effectively enhance the hydrophilicity of FNS-1 and FNS-2. Due to the hydrophobic -CH3 group and the smaller adsorption amount, FNS-1 possesses a weaker hydrophilic modification ability than FNS-2. Investigating the adsorption behavior of fluorocarbon surfactants on the PTFE surface can help us to better utilize fluorocarbon surfactants. This could have broad implications for colloid and interface science.

Optothermal‐Enabled Reconfigurable Colloidal Photonic Crystals for Color and Spectrum Manipulation

AbstractColloidal photonic crystals (CPCs) are extensively utilized in nanoscale light manipulation due to their periodic dielectric structure. However, achieving spatial reconfigurability in CPCs remains a significant challenge, despite its importance for broader photonic applications in colloidal science. In this study, an optically induced thermoelectric field is generated by adding ionic surfactants to the solution, leading to the efficient formation of tightly assembled nanoparticles that exhibit the characteristics of CPC, which is termed optothermo‐CPC. Specifically, this CPC exhibits excellent spatial reconfigurability through the tuning of the optically induced thermoelectric field. This allows for the remote control of its position and shape, in a real‐time and high‐precision manner. Additionally, by changing the particle size, it is possible to tune the transmission spectrum and color. Additionally, optothermo‐CPC can navigate obstacles and possess a robust self‐healing ability. These highly adaptable and reconfigurable properties endow CPCs with significant potential for various photonic applications within complex fluidic environments.

Using Rheology and Image Processing to Study the Effects of Cellulose Nanocrystal Sedimentation.

The effect of sedimentation on lyotropic liquid crystalline dispersions is both an interesting subject in colloidal science and is of practical importance for understanding changes that can occur during dispersion storage. This research explored how the seemingly subtle changes in average length resulting from a single sedimentation step affected the rheological properties and self-assembly of aqueous dispersions of sulfated cellulose nanocrystals. Sedimentation of a primarily isotropic aqueous cellulose nanocrystal dispersion for 1 month at ambient conditions resulted in an isotropic top phase and a biphasic bottom phase, which were separated for further study. Both atomic force microscopy measurements and intrinsic viscosities determined via Fedor's equation showed preferential fractionation of longer cellulose nanocrystals (CNCs) to the bottom phase. The effects of this fractionation on dispersion rheology and phase behavior were studied by preparing a range of concentrations from each phase. As expected, the concentration for the isotropic-biphasic phase transition was significantly lower for the bottom phase than for the top phase or parent dispersion. Rheological changes were generally subtle, but significant differences were seen in the storage modulus at concentrations approaching rheological gelation. Most notably, quantitative image processing showed that even this simple, single-step fractionation process had a significant impact on the relative proportion of tactoids and chiral helices with planar and homeotropic anchoring in self-assembled cellulose nanocrystal films. These results highlight the impact that changes in polydispersity due to sedimentation can have on the self-assembly of nanomaterial mesogens.

Einstein–Perrin dilemma on the Brownian motion (Avogadro’s number) resolved?

The general recognition of the existence of atoms and molecules occurred only at the beginning of the twentieth century. Many researchers contributed to this, but the ultimate proof of the molecular nature of matter that convinced even the last sceptics was the confirmation of Albert Einstein’s statistical-fluctuation theory of Brownian motion, a part of his comprehension of interdisciplinary atomism, by Jean Perrin’s experiments on colloidal gamboge particles. Einstein noticed a difference between the values of Avogadro’s constant derived from Perrin’s experiments and Planck’s calculation from black-body radiation. Einstein assumed the incorrectly evaluated size of the gamboge spherules to be a culprit of the difference and asked Perrin to check the assumption with additional experiments and using the viscosity formula introduced in his own dissertation. The result was a discrepancy that neither Einstein nor Perrin settled any further. In this communication, based on the survey of developments in colloid and polymer science and their comparison with relevant experiments, an explanation of the dilemma is given that now, after more than a century, proves Einstein correct. The comparison was de facto possible during his lifetime.

On the self-similarity of unbounded viscous Marangoni flows

The Marangoni flow induced by an insoluble surfactant on a fluid–fluid interface is a fundamental problem investigated extensively due to its implications in colloid science, biology, the environment and industrial applications. Here, we study the limit of a deep liquid subphase with negligible inertia (low Reynolds number, $Re\ll {1}$ ), where the two-dimensional problem has been shown to be described by the complex Burgers equation. We analyse the problem through a self-similar formulation, providing further insights into its structure and revealing its universal features. Six different similarity solutions are found. One of the solutions includes surfactant diffusion, whereas the other five, which are identified through a phase-plane formalism, hold only in the limit of negligible diffusion (high surface Péclet number $Pe_s\gg {1}$ ). Surfactant ‘pulses’, with a locally higher concentration that spreads outward, lead to two similarity solutions of the first kind with a similarity exponent $\beta =1/2$ . On the other hand, distributions that are locally depleted and flow inwards lead to similarity of the second kind, with two different exponents that we obtain exactly using stability arguments. We distinguish between ‘dimple’ solutions, where the surfactant has a quadratic minimum and $\beta =2$ , from ‘hole’ solutions, where the concentration profile is flatter than quadratic and $\beta =3/2$ . Each of these two cases exhibits two similarity solutions, one valid prior to a critical time $t_*$ when the derivative of the concentration is singular, and another one valid after $t_*$ . We obtain all six solutions in closed form, and discuss predictions that can be extracted from these results.

Adsorption, Aggregation, and Application Properties of Green Pluronic Aliphatic Alcohol Ether Carboxylic Acids and Nonionic/Amphoteric Surfactants in Water.

In the realm of colloid and interface science, new types of green surfactants, including anionic Pluronic alcohol ether carboxylate (AEC), branched alkyl glucoside (IG), and zwitterionic coconut oil amide propyl betaine (CAB), have been identified and merit further exploration. AEC, characterized by its inclusion of 5 EO and 3.5 PO units, was synthesized, and its behavior in aqueous solutions with IG and CAB was meticulously examined. Their performance in applications such as foam generation, wetting, and the dispersion and stabilization of graphene was also evaluated. At αAE5P3C = 0.5, AE5P3C/CAB exhibited superior surface and interfacial properties compared to AE5P3C/IG. In these hybrid systems, the self-assembly of micelles is predominantly influenced by hydrogen bonding, electrostatic interactions, and hydrophobic forces. Kinetic analysis further confirmed that the driving force for micelle formation in these hybrid systems is enthalpy, with the adsorption process involving a mixed diffusion-kinetic adsorption mechanism. AE5P3C/CAB demonstrated enhanced foaming ability, foam stability, and wetting properties compared to AE5P3C/IG. Intriguingly, the optimal dispersion and stabilization of graphene were achieved with AE5P3C/IG at αAE5P3C = 0.2, providing a foundational basis for its potential application in graphene-based systems. A thorough examination of the synergistic mechanisms and application potential of these three distinct surfactants in aqueous solutions was presented, taking into account various charged ions and the specific hydrophilic and hydrophobic groups of EO and PO. This study not only provides fundamental insights into their intrinsic properties but also offers a fresh perspective for the ongoing exploration of green surfactants.

The Poisson–Boltzmann equation in micro- and nanofluidics: A formulary

The Poisson–Boltzmann (PB) equation provides a mean-field theory of electrolyte solutions at interfaces and in confinement, describing how ions reorganize close to charged surfaces to form the so-called electrical double layer (EDL), with numerous applications ranging from colloid science to biology. This formulary focuses on situations of interest for micro- and nanofluidics, and gathers important formulas for the PB description of a Z:Z electrolyte solution inside slit and cylindrical channels. Different approximated solutions (thin EDLs, no co-ion, Debye–Hückel, and homogeneous/parabolic potential limits) and their range of validity are discussed, together with the full solution for the slit channel. Common boundary conditions are presented, the thermodynamics of the EDL is introduced, and an overview of the application of the PB framework to the description of electrokinetic effects is given. Finally, the limits of the PB framework are briefly discussed, and Python scripts to solve the PB equation numerically are provided.

Precursor-film-driven ultra-early depinning of the three-phase contact line

Hypothesis: Despite its importance in colloid and interface science, contact line pinning remains poorly understood, especially in the presence of a precursor film. We hypothesized that this is due to a lack of an experimental method capable of directly observing their physics at the nanoscale. MethodsUsing coherence scanning interferometry, we visualized the three-dimensional behavior of contact lines with a precursor film near a nanogroove structure composed of flat terrace surfaces and steps with an inclination angle of 30° while achieving nanoscale vertical resolution. FindingsWe found that even when the contact line is pinned at the edge of the step, the precursor film is not and advances beyond the edge. Furthermore, we discovered that the precursor film has two distinct effects on contact line motion. Specifically, the precursor film facilitates depinning when the contact line descends the step — a contact angle change was 0.9°, only 3.0% of the value predicted by a classical theory of contact angle at a solid edge. This ultra-early depinning is attributed to the formation of a new liquid film past the edge, driven by the progression of the precursor film that overcomes the pinning effect. In contrast, when the contact line ascends the step, the precursor film acts as a resistance to movement due to steric interaction.

Leveraging colloid and interface science for long-term marine performance of hybrid coatings: Effects of different nanoparticles on anticorrosion and antifouling properties

This study leveraged the unique colloidal and interfacial properties of synthesized SiO2, ZnO, and carbon (CN) nanoparticles as effective nanofillers to enhance the anti-corrosion and antifouling properties of PMMA coatings. By optimizing nanoparticle dispersion, stability, and functional performance within the polymer matrix, we achieved improved surface roughness, hydrophobicity, mechanical stability, and antimicrobial properties. Hybrid coatings containing 1.5 wt% of these nanoparticles were applied to stainless steel (SS) substrates and evaluated through water contact angle measurements, pull-off adhesion strength tests, antibacterial assays, and electrochemical impedance spectroscopy (EIS). The results demonstrate that the synergistic effects of SiO2, ZnO, and CN nanoparticles significantly enhance the coatings' anticorrosion and antifouling characteristics by increasing hydrophobicity, total impedance, and antibacterial activity via reactive oxygen species generated by ZnO and CN. Additionally, over two years, the coating’s long-term protection was assessed by submerging coupons at a 6-meter depth in the Bocana Chica reef barrier, a site with rapid biofouling colonization, making this test a demanding evaluation.

Response to the comments on “Cellular aggregation dictates universal spreading behaviour of a whole-blood drop on a paper strip”

In 2023, we published a research article in the Journal of Colloidal and Interface Science, based on our experimental findings and substantiating scaling arguments leading to a simple theoretical insight on the effect of red blood cell (RBC) aggregation on the wicking behaviour of a finite volume of blood as it navigates through the porous passages of a paper matrix (Laha et al., 2023). Of late, we received comments from Li (2024), which offered certain suggestions regarding the possible improvement of the capillary bundle model as considered in our article for analyzing the transport of blood through the paper pores. Herein, we provide a detailed discussion on each of the points raised by Li (2024) and rationalize our views in further details in addition to the contents already provided in our concerned article.

Bridging Technology and Environment: Sustainable Approaches in Semiconductor Chemical Mechanical Planarization (CMP)

As semiconductor technologies continue to advance in areas such as autonomous driving, artificial intelligence, 5G communications, the Internet of Things, and large-scale data processing, the demand for a reliable semiconductor industry is on the rise.(1) This growing demand necessitates the use of advanced device architectures, which heavily rely on two crucial processes: Chemical Mechanical Planarization (CMP) and post-CMP cleaning.(2) This talk will focus on the development of CMP slurries and post-CMP cleaning solutions, emphasizing their vital roles in these processes. We will delve into the comprehensive development of CMP slurries and post-CMP cleaning solutions, highlighting how synthesis methods can significantly affect the surface chemistry of ceria abrasives and impact the removal rates of SiO2 surfaces during STI CMP.(3, 4) Our research also demonstrates how our cleaning solutions can effectively remove even the most 10 nm-sized ceria particles from SiO2 surfaces,(5) thereby enhancing process efficiency. Furthermore, we will discuss the use of aliphatic amino acids as environmentally friendly corrosion inhibitors in CMP slurries, offering a sustainable alternative to the traditionally used benzotriazole (BTA) and addressing key environmental challenges.(6) In the context of the rapidly expanding semiconductor industry, it becomes critical to address global sustainability concerns and environmental health and safety (EHS) objectives. Our research proposes a comprehensive methodology for evaluating the sustainability of CMP consumables in semiconductor manufacturing, with a primary focus on CMP slurries due to their significant market share and shorter usage lifetimes. This research serves as a foundation for future CMP sustainability analyses, encouraging self-correction strategies within the CMP community to reduce environmental impact. We will also introduce a robust framework for the Life Cycle Assessment (LCA) of CMP consumables, marking a crucial step toward achieving these sustainability goals. In summary, this talk will explore the intricate details of CMP and post-CMP processes, their pivotal roles in the advancement of semiconductor manufacturing, and the imperative task of aligning these processes with environmental and sustainability objectives.This talk is dedicated to the special session in honor of Prof. Babu. S. Babu, Advances in Chemical Mechanical Planarization (CMP), Woodhead Publishing (2021).J. Seo, Journal of Materials Research, 36, 235 (2021).J. Seo, J. W. Lee, J. Moon, W. Sigmund and U. Paik, ACS applied materials & interfaces, 6, 7388 (2014).J. Seo, J. H. Kim, M. Lee, J. Moon, D. K. Yi and U. Paik, Journal of colloid and interface science, 483, 177 (2016).J. Seo, A. Gowda and S. Babu, ECS Journal of Solid State Science and Technology, 7, P243 (2018).H. T. T. Tran, J. Gichovi, E. J. Podlaha and J. Seo, in Electrochemical Society Meeting s 243, p. 1809 (2023).

Deconvoluting Surface Modification Effects on Flow Battery Electrode Performance by Impedance Spectroscopy

Flow batteries have proliferated over the past decade, both in installed capacity and in the diversity of systems being developed for grid storage applications. As a long duration energy storage technology, flow batteries offer the distinct advantage of independent scaling of energy capacity through their liquid electrolytes, and of power capacity through stack design. Across flow battery systems, improving the design of reactor stacks to achieve high power densities at acceptable energy conversion efficiencies remains an important lever for lowering overall levelized costs of storage. In pursuit of this aim, understanding the reaction kinetics on the surfaces of porous carbon electrodes is key [1]. However, traditional techniques such as voltammetry, impedance spectroscopy, and cell performance must be utilised with caution to avoid convoluting observations of surface kinetics with other effects.Previous studies on vanadium flow batteries have used impedance spectroscopy to circumvent this issue, utilising the shared dependence of double layer capacitance and charge transfer conductance [2]. In recent years, DRT analysis of impedance spectra has also been used to further study electrode treatments for vanadium systems [3]. Building on these works, we use impedance spectroscopy combined with other techniques to deconvolute the effects of electrode treatments ex-situ before demonstrating the modified electrode performance in flow cells. The accompanying abstract image illustrates how different electrode modifications can manifest comparative differences in identified faradaic features in impedance spectra. As the most well studied system, we first apply our analysis to electrodes for vanadium electrolytes, validating our method and previous studies on electrode modifications. Following this, we apply our approach to capture a range of behaviours by studying redox active species with faster kinetics, such as recently developed organic species [4].The results of this work aim to improve the evaluation of reaction kinetics for different redox active species and electrode treatments. By doing so, we seek to further understand surface reaction mechanisms and how they can be harnessed to improve stack and electrolyte performance.[1] T. V. Sawant, C. S. Yim, T. J. Henry, D. M. Miller, and J. R. McKone, ‘Harnessing Interfacial Electron Transfer in Redox Flow Batteries’, Joule, vol. 5, no. 2, pp. 360–378, Feb. 2021, doi: 10.1016/j.joule.2020.11.022.[2] H. Fink, J. Friedl, and U. Stimming, ‘Composition of the Electrode Determines Which Half-Cell’s Rate Constant is Higher in a Vanadium Flow Battery’, J. Phys. Chem. C, vol. 120, no. 29, pp. 15893–15901, Jul. 2016, doi: 10.1021/acs.jpcc.5b12098.[3] K. Köble et al., ‘Revealing the Multifaceted Impacts of Electrode Modifications for Vanadium Redox Flow Battery Electrodes’, ACS Appl. Mater. Interfaces, vol. 15, no. 40, pp. 46775–46789, Oct. 2023, doi: 10.1021/acsami.3c07940.[4] J.-M. Fontmorin, S. Guiheneuf, T. Godet-Bar, D. Floner, and F. Geneste, ‘How anthraquinones can enable aqueous organic redox flow batteries to meet the needs of industrialization’, Current Opinion in Colloid & Interface Science, vol. 61, p. 101624, Oct. 2022, doi: 10.1016/j.cocis.2022.101624. Figure 1

Surface Engineered Ni-Fe Foam As a Bi-Functional Electrode for Water Electrolysis in Alkaline Media

Using fossil fuels as a main source of energy has resulted in various environmentally hazardous effects, including global warming, climate change, and environmental pollution. Consequently, the development of a sustainable and clean source of energy became of urgent need. Water electrolysis has captured considerable attention as the main technology of hydrogen fuel production. It is particularly enticing due to its eco-friendliness and sustainability. Self-supported electrocatalysts for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) have prominent roles in water electrolysis. Growing self-supported metal oxides, hydroxides1, phosphates2, sulfides3, etc. that possess high electrical conductivity, electrocatalytic activity, and structural stability have attracted attention lately. FeNi-based catalysts are considered one of the most promising electrocatalysts for water electrolysis in alkaline solutions. However, improving their catalytic activity and stability is one of the research targets before further practical applications. Nickel foam is widely used as a self-supported electrocatalyst due to its high surface area, low cost, and exceptional catalytic activity, with several studies focused on the deposition of nickel-iron materials on nickel foam for the development of a bifunctional catalyst for water electrolysis4. However, very few studies used NiFe mesh or foam to grow a self-supported catalyst material5.In this study, surface-engineered NiFe foam electrodes were developed by facile control of the Ni/Fe surface ratio via chemical leaching and oxidation with NaOH and NaClO4 followed by electrochemical activation, aiming to design a bifunctional electrocatalyst for both OER and HER. Results revealed that varying the ratios of NaOH and NaClO4 induced significant alterations to the surface composition (different Ni/Fe), and hence the active sites for OER and HER. The physicochemical and structural properties of the NiFe foam were characterized using glancing angle X-ray diffraction (GAXRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscope (SEM). Further, the catalytic activity of the modified electrode was assessed utilizing cyclic voltammetry, linear sweep voltammetry, chronopotentiometry, and electrochemical impedance spectroscopy. References F. Dionigi and P. Strasser, Advanced Energy Materials, 6, 1600621 (2016).Y. Yu et al., Journal of Colloid and Interface Science, 607, 1091–1102 (2022).A. Shankar, R. Elakkiya, and G. Maduraiveeran, New J. Chem., 44, 5071–5078 (2020).H.-S. Hu, S. Si, R.-J. Liu, C.-B. Wang, and Y.-Y. Feng, International Journal of Energy Research, 44, 9222–9232 (2020).C. Sun et al., ACS Appl. Energy Mater., 4, 8791–8800 (2021).

Photoswitchable Surfactants–Are there Alternatives to Azobenzene‐Based Systems?

AbstractOwing to their property to alter their surface‐activity upon the irradiation with light, photoswitchable surfactants have gained tremendous interest in colloidal science. Their mere addition to a colloidal system allows, e. g., to obtain control over polyelectrolytes, micro‐ and nanoscale particles or emulsions. Most literature examples focus on azobenzene‐based, or related, systems, which employ a photoisomerization reaction for switching. Other structures, such as spiropyrans, play a subordinate role, although they have gained increasing attention over the past few years. In this perspective article, we want to provide an overview about existing systems of photoswitchable surfactants. We address the issue that alternative photoswitches are given less attention, and what benefits surfactants could possess that are based on said switchable units. With our contribution, we want to broaden the view on stimuli‐responsive surfactants – and to provide a guideline for the design of novel structures.

Tuning Lubrication Performance of Phase‐changing Emulsion‐filled Gels by Sugar alcohols

Lubrication by hydrogels is proving to be an emerging area in colloid science. Although oil‐driven friction reduction is predominant in literature, emulsion gel‐based lubrication has attracted very little attention to date. We hypothesize that an interplay of viscolelasticity and oil volume fraction may modulate lubricity of emulsion‐filled gels. Herein, phase‐change gelatin‐based emulsion‐filled gels with different sugar alcohol and oil droplet concentrations (0‐30 wt%) were tested for their lubrication performance. The rheological and tribological tests were analysed in conjunction with spectroscopic and structural characterizations in order to reveal structure‐function relationship. Structural characterizations demonstrated that hydrogen bonding was enhanced in pure gelatin gels with the increase of sugar alcohol (glycerol)‐replacement time, which enhanced the storage modulus (G') of the gel networks. Emulsified droplets served as active fillers further strengthening the G’ and strikingly the presence of glycerol reduced the thermo‐responsiveness of the emulsion‐filled gels. Emulsion‐filled gels containing sugar alcohols, irrespective of their type, can greatly reduce the friction coefficients (μ) between hydrophobic surfaces in the boundary and mixed regimes versus the systems without sugar alcohols. In the hydrodynamic regime, the friction coefficient of the system was proportional to the second plateau shear viscosity, regulated by the oil content.This article is protected by copyright. All rights reserved.

Exploring proteins at soft interfaces and in thin liquid films – From classical methods to advanced applications of reflectometry

The history of the topic of proteins at soft interfaces dates back to the 19th century, and until the present day, it has continuously attracted great scientific interest. A multitude of experimental methods and theoretical approaches have been developed to serve the research progress in this large domain of colloid and interface science, including the area of soft colloids such as foams and emulsions. From classical methods like surface tension adsorption isotherms, surface pressure-area measurements for spread layers, and surface rheology probing the dynamics of adsorption, nowadays, advanced surface-sensitive techniques based on spectroscopy, microscopy, and the reflection of light, X-rays and neutrons at liquid/fluid interfaces offers important complementary sources of information. Apart from the fundamental characteristics of protein adsorption layers, i.e., surface tension and surface excess, the nanoscale structure of such layers and the interfacial protein conformations and morphologies are of pivotal importance for extending the depth of understanding on the topic. In this review article, we provide an extensive overview of the application of three methods, namely, ellipsometry, X-ray reflectometry and neutron reflectometry, for adsorption and structural studies on proteins at water/air and water/oil interfaces. The main attention is placed on the development of experimental approaches and on a discussion of the relevant achievements in terms of notable experimental results. We have attempted to cover the whole history of protein studies with these techniques, and thus, we believe the review should serve as a valuable reference to fuel ideas for a wide spectrum of researchers in different scientific fields where proteins at soft interface may be of relevance.

Spearheading a new era in complex colloid synthesis with TPM and other silanes.

Colloid science has recently grown substantially owing to the innovative use of silane coupling agents (SCAs), especially 3-trimethoxysilylpropyl methacrylate(TPM). SCAs were previously used mainly as modifying agents, but their ability to form droplets and condense onto pre-existing structures has enabled their use as a versatile and powerful tool to create novel anisotropic colloids with increasing complexity. In this Review, we highlight the advances in complex colloid synthesis facilitated by the use of TPM and show how this has driven remarkable new applications. The focus is on TPM as the current state-of-the-art in colloid science, but we also discuss other silanes and their potential to make an impact. We outline the remarkable properties of TPM colloids and their synthesis strategies, and discuss areas of soft matter science that have benefited from TPM and other SCAs.

Physicochemical Properties and Functionalities of Food Emulsifiers

Purpose: This study sought to analyze the physiochemical properties and functionalities of food emulsifiers. Methodology: The study adopted a desktop research methodology. Desk research refers to secondary data or that which can be collected without fieldwork. Desk research is basically involved in collecting data from existing resources hence it is often considered a low cost technique as compared to field research, as the main cost is involved in executive’s time, telephone charges and directories. Thus, the study relied on already published studies, reports and statistics. This secondary data was easily accessed through the online journals and library. Findings: The findings reveal that there exists a contextual and methodological gap relating to the physiochemical properties and functionalities of food emulsifiers. Preliminary empirical review revealed that the importance of considering emulsifier properties in food product development. The findings underscored the significance of optimizing emulsifier selection and formulation to meet consumer demands for healthier, more sustainable, and better-performing food products. Continued research in this area promises to drive further innovation and advancements in food technology. Unique Contribution to Theory, Practice and Policy: The Interfacial Tension theory, HLB (Hydrophilic- Lipophilic Balance) theory and Emulsion Phase Inversion theory may be used to anchor future studies on the physiochemical properties and functionalities of food emulsifiers. The study made significant contributions to theoretical understanding, practical application, and policy considerations in the field of food science and technology. It advanced theoretical knowledge by exploring molecular mechanisms and integrating principles from colloid and interface science. In practice, the study recommended systematic approaches for emulsifier selection and process optimization to enhance product quality and consistency. From a policy perspective, it emphasized the importance of regulatory guidelines and transparency in emulsifier usage. Additionally, the study advocated for sustainability, innovation, and consumer-centric approaches to promote environmental responsibility, drive technological advancements, and prioritize consumer well-being in emulsifier research and application.

Range and sensitivity of 17O nuclear spin-lattice relaxation as a probe of aqueous electrolyte dynamics.

The study of electrolytic solutions is of relevance in many research fields, ranging from biophysics, materials, and colloid science to catalysis and electrochemistry. The dependence of solution dynamics on the nature of electrolytes and their concentrations has been the subject of many experimental and computational studies, yet it remains challenging to obtain a full understanding of the factors that govern solution behavior. Here, we provide additional insights into the behavior of aqueous solutions of alkali chlorides by combining 17O relaxation data with diffusion and viscosity data and contrast their behavior with 1H nuclear magnetic resonance relaxation data. The main findings are that 17O relaxation correlates well with viscosity data but not with diffusion data, while 1H relaxation correlates with neither. Certain ionic trends match known ion-specific series behavior, especially at high concentrations. Notably, we also examine the ranges of the interactions and conclude that the majority of the effects are tied to local water reorientation dynamics.

Improving the sensing sensitivity of silver nanoparticle-based colorimetric biosensors from the point of salt.

The sensing sensitivity was improved for silver nanoparticles (AgNPs)-based colorimetric biosensors by using the most suitable salt to induce AgNPs aggregation. As for the salt composed of low-affinity anion and monovalent cation, the cation-dependent charge screening effect was the driving force for AgNPs aggregation. Apart from the charge screening effect, both the bridging of multivalent cation to the surface ligand of AgNP and the interaction between anion and Ag contributed to inducing AgNPs aggregation. Considering the higher aggregation efficiency of AgNPs resulted in a narrower sensing range, salt composed of low-affinity anion and monovalent cation was recommended for AgNPs-based colorimetric analysis, which was confirmed by fourfold higher sensitivity of DNA-21 detection using NaF than NaCl. This work inspires further thinking on improving the sensing performanceof metal nanomaterials-based sensors from the point of colloidal surface science.