Temperature-dependent Changes Research Articles

A novel proxy for energy flux in multi-era wildfire reconstruction

Escalations in wildfire activity are of significant global concern, particularly within vulnerable wetland ecosystems integral to natural carbon sequestration and climate change mitigation. Our understanding and management of future wildfire activity may be better contextualised through the study of historic and ancient fire records, independent of human influence. Methods of study include ‘geothermometry’ - approximating ancient fire intensity from temperature-dependent changes in the chemistry of fossil charcoal. Though well established in their relation to experimental charcoalification, these methods still fail to quantify the true intensity of ancient fires, as a measure of energy release. As a result, their applicability, and contributions to the characterisation of modern fire activity, remain uncertain. Here, we present a novel measure of wildfire energy release, as a proxy for true intensity, through the co-application of cone calorimetry and Raman spectroscopy of charcoal. By applying a range of wildfire heat fluxes to variable peatland fuel mixes, this research demonstrates the complexity in correlating fire behaviour and charcoal microstructure. Further statistical analyses suggest a correlation between spectroscopic results, measures of CO and CO2 release, and fire severity. This offers a principal measure of ancient wildfire intensity, consistent with modern practices in wildfire modelling, monitoring, and management.

Luminescence Thermochromism of a Noncluster Copper Iodide Complex.

Hybrid copper(I) halide materials are currently attracting significant attention due to their exceptional luminescence properties, offering great potential for the development of multifunctional emissive materials with, in addition, eco-friendly features. A binuclear copper iodide complex, based on the [Cu2I2L4] motif with phosphite derivatives as ligands, has been synthesized and structurally characterized. Photophysical investigations indicate that this complex displays luminescence thermochromic properties, which are characterized by a temperature-dependent change in the relative intensity of two emission bands. The high-contrast luminescence thermochromism, with an important color variation from purple to cyan, is ascribed to the thermal equilibrium of two different excited states. While thermochromism is relatively known for multimetallic complexes, the perfectly controlled thermochromism of the studied compound is unprecedented for a binuclear complex. From theoretical investigations, this original feature is due to the coordination of phosphite ligands, which induces a specific energy layout of the complex, presenting vacant orbitals of varying nature. This single-component, dual-emissive binuclear complex, displaying relevant sensitivity temperature response, presents great potential for luminescence ratiometric thermometry applications. This study underlines the relevance of the ligand engineering strategy in developing original, emissive, and sustainable copper-based materials.

Temperature dependent effect of nano-scale phase change materials on fresh and hardened cement based mortar

One of the smart and innovative materials used to produce environmentally friendly energy-saving concrete is temperature dependent phase change (PCM) materials. In this study, the fresh and hardened concrete properties of the mortars including PCM in different ratios (0%, 2.5%, 5%) were investigated experimentally. Rheological properties such as slump-flow, specific viscosity, and yield stress tests were determined at different temperatures (from 20 to 50 °C). Time-dependent physical, mechanical, and thermal properties such as ultrasound pulse velocity (UPV), electrical resistivity, dynamic modulus of elasticity, compressive and flexural strength, thermogravimetric (TGA), and thermal conductivity tests were carried out. According to the experimental findings, the workability and hardened properties of mortars were decreased by using PCM. However, the rheological properties of fresh mortar change depending on temperature due to PCM absorbing the heat. Therefore, the fresh properties of mortar with PCM can be controlled by temperature. It was also found that the phase change of mortars with PCM can be obtained by measuring the electrical or UPV tests at different temperatures.

Chlorophyll and Carotenoid Metabolism Varies with Growth Temperatures among Tea Genotypes with Different Leaf Colors in Camellia sinensis

The phenotype of albino tea plants (ATPs) is significantly influenced by temperature regimes and light conditions, which alter certain components of the tea leaves leading to corresponding phenotypic changes. However, the regulatory mechanism of temperature-dependent changes in photosynthetic pigment contents and the resultant leaf colors remain unclear. Here, we examined the chloroplast microstructure, shoot phenotype, photosynthetic pigment content, and the expression of pigment synthesis-related genes in three tea genotypes with different leaf colors under different temperature conditions. The electron microscopy results revealed that all varieties experienced the most severe chloroplast damage at 15 °C, particularly in albino cultivar Baiye 1 (BY), where chloroplast basal lamellae were loosely arranged, and some chloroplasts were even empty. In contrast, the chloroplast basal lamellae at 35 °C and 25 °C were neatly arranged and well-developed, outperforming those observed at 20 °C and 15 °C. Chlorophyll and carotenoid measurements revealed a significant reduction in chlorophyll content under low temperature treatment, peaking at ambient temperature followed by high temperatures. Interestingly, BY showed remarkable tolerance to high temperatures, maintaining relatively high chlorophyll content, indicating its sensitivity primarily to low temperatures. Furthermore, the trends in gene expression related to chlorophyll and carotenoid metabolism were largely consistent with the pigment content. Correlation analysis identified key genes responsible for temperature-induced changes in these pigments, suggesting that changes in their expression likely contribute to temperature-dependent leaf color variations.

Diffusion in Polymethylene Chain Solutions with a Polar Component.

A hydrodynamic bead model based on Kirkwood-Riseman theory has been used to calculate the translational diffusion constant, D, for solutes with polymethylene chains in solutions with a polar component. A comparison with the experimental values for nonpolar n-alkanes in polar 2-propanol, tetrahydrofuran, chlorobenzene, chloroform, 1-octanol, quinoline, and chloroform (78 D values) and polar primary alcohols in nonpolar benzene and n-octane (24 D values) gives an average absolute percentage difference of ∼3% between the 102 experimental and calculated D values. Consideration of the solvent's temperature-dependent changes in the degree of aggregation due to hydrogen bonding was necessary for the n-alkanes in 1-octanol. Good agreement was not found for primary alcohols in 1-octanol due to solute-solvent hydrogen bonding. A correlation that depends on the solutes' molar volumes instead of their chain lengths gives worse agreement than the bead model for the n-alkanes in polar solvents and primary alcohols and n-alkanes in nonpolar solvents.

Adsorption and removal of herbicide paraquat from aqueous solutions via novel bimetal organic framework: Kinetics, equilibrium and statistical surface modeling

This study examines the adsorption and removal of the herbicide paraquat in relation to a bimetal organic framework known as the Terbium/Palladium Metal-Organic Framework (Tb/Pd-MOF). Analysis of N2 adsorption/desorption isotherms, which were used to assess the properties of the Tb/Pd-MOF, revealed that the absorption of paraquat on Tb/Pd-MOF resulted in a reduction in pore volume, pore size, and surface area. Specifically, the pore volume decreased from 8.25 to 5.68 cm3/g, the pore size decreased from 11.34 nm to 8.92 nm, and the surface area decreased from 1456.61 to 1262.82 m2/g. The pore radius also decreased from 0.96 nm to 0.58 nm. Tb/Pd-MOF’s functional groups were identified through FT-IR, and the structure of the compound was confirmed using XPS. Various adsorption parameters including temperature, adsorbent dosage, pH, paraquat concentration, and contact time were studied. Density functional theory (DFT) was used to understand the electrical properties, reactivity, and morphology of paraquat. Results from the DFT analysis revealed that the electrophilic and nucleophilic attack sites aligned with the molecular orbitals (HOMO and LUMO) and MEP outcomes. The study found that Tb/Pd-MOF demonstrated a significant absorption capacity for paraquat, with adsorption data consistent with the Langmuir isotherm and pseudo-second-order kinetic models. The paraquat adsorption capability of Tb/Pd-MOF was determined to be 574.8 mg/g. Furthermore, chemisorption was identified as the primary form of adsorption, as indicated by the adsorption energy of 26.98 kJ·mol−1. The optimal conditions for achieving a high adsorption capacity were identified as pH 8 and 0.02 g of Tb/Pd-MOF. The temperature-dependent changes in the thermodynamic parameters ΔG°, ΔH°, and ΔS° indicated that the paraquat absorption onto Tb/Pd-MOF occurred spontaneously, was endothermic, and involved random processes. To optimize the absorption process, Response Surface Methodology and Box-Behnken design (RSM, BBD) were employed. These techniques enabled effective removal of paraquat from the Tb/Pd-MOF material. During chemisorption, the adsorbate and adsorbent form chemical bonds, while aromatic rings are involved in π-π bonding. Additionally, pore-filling occurs when the adsorbate fills the pores of the adsorbent, and electrostatic interactions result from the attraction or repulsion of charges between the adsorbate and adsorbent. As a means of eliminating paraquat from wastewater, Tb/Pd-MOF demonstrates significant potential due to its diverse absorption processes and high capacity for adsorption.

Temperature-dependent generalized ellipsometry of the metal–insulator phase transition in low-symmetry charge-transfer salts

Determining the optical and electronic properties of strongly anisotropic materials with symmetries below orthorhombic remains challenging; generalized ellipsometry is a powerful technique in this regard. Here, we employ Mueller matrix spectroscopic and temperature-dependent ellipsometry to determine the frequency dependence of six components of the dielectric-function tensor of the two-dimensional charge-transfer salt α-(BEDT-TTF)2I3 across its metal–insulator transition. Our results offer valuable insights into temperature-dependent changes of the components of the spectroscopic dielectric-function tensor across the metal–insulator transition. This advanced method allows extension to other electronic transitions.

A finite volume approximations for one nonlinear and nonlocal integrodifferential equations

In this paper, the error analysis of the Petrov–Galerkin finite volume element method (FVEM) is investigated for a nonlinear parabolic integro-differential equation that arises in the mathematical modeling of the penetration of a magnetic field into a substance, accounting for temperature-dependent changes in electrical conductivity. Starting from Maxwell’s equations, we derive a one-dimensional model problem, which forms the basis of our analysis. Our main goal is to develop a general framework for obtaining finite volume element approximations and to study the error analysis. For simplicity, we consider only the lowest-order (linear and L-splines) finite volume elements. The novel contribution lies in the application of FVEM to this problem, leading to the establishment of an unconditionally stable numerical scheme and the derivation of optimal error estimates in the L∞(L2(Ω)) and L2(H01(Ω)) norms for both semi-discrete and linearized backward Euler fully-discrete schemes, using a generalized projection method that carefully manages the nonlinear terms. Lastly, numerical experiments are provided to support the theoretical conclusions.

SARS-CoV-2 Variants from Long-Term, Persistently Infected Immunocompromised Patients Have Altered Syncytia Formation, Temperature-Dependent Replication, and Serum Neutralizing Antibody Escape.

SARS-CoV-2 infection of immunocompromised individuals often leads to prolonged detection of viral RNA and infectious virus in nasal specimens, presumably due to the lack of induction of an appropriate adaptive immune response. Mutations identified in virus sequences obtained from persistently infected patients bear signatures of immune evasion and have some overlap with sequences present in variants of concern. We characterized virus isolates obtained greater than 100 days after the initial COVID-19 diagnosis from two COVID-19 patients undergoing immunosuppressive cancer therapy, wand compared them to an isolate from the start of the infection. Isolates from an individual who never mounted an antibody response specific to SARS-CoV-2 despite the administration of convalescent plasma showed slight reductions in plaque size and some showed temperature-dependent replication attenuation on human nasal epithelial cell culture compared to the virus that initiated infection. An isolate from another patient-who did mount a SARS-CoV-2 IgM response-showed temperature-dependent changes in plaque size as well as increased syncytia formation and escape from serum-neutralizing antibodies. Our results indicate that not all virus isolates from immunocompromised COVID-19 patients display clear signs of phenotypic change, but increased attention should be paid to monitoring virus evolution in this patient population.

Improving the computational performance of district heating network simulation

ABSTRACT District heating and cooling (DHC) systems are gaining importance due to their ability to integrate renewable and waste heat sources and connect with other infrastructures. However, the complexity of DHC systems rises as technical components and potential interactions grow, and energy demands increase. Heat transportation via water flow involves time- and temperature-dependent changes based on mass flow rates and heat losses, influenced by the dynamic properties of consumers and distribution pipes. To optimise DHC operations and simulate their complexities, dynamic modelling tools are necessary. However, dynamically simulating large-scale DHC networks are computationally demanding. One method to improve district heating networks (DHNs) is to replace dynamic pipe models with static models, simplifying the network's topological complexities. This paper proposes a framework for simulating DHNs using the NetworkX Python package to create and manipulate complex networks and the Modelica environment to simulate physical systems. The study highlights the constraints of the pipe replacement workflow due to its dependence on seasonal variation. The findings indicate that replacing pipe models can reduce CPU time by 30% to 65% in simulations, depending on the required accuracy during the summer season.

Predicting population-level impacts of projected climate heating on a temperate freshwater fish.

Climate heating has the potential to drive changes in ecosystems at multiple levels of biological organization. Temperature directly affects the inherent physiology of plants and animals, resulting in changes in rates of photosynthesis and respiration, and trophic interactions. Predicting temperature-dependent changes in physiological and trophic processes, however, is challenging because environmental conditions and ecosystem structure vary across biogeographical regions of the globe. To realistically predict the effects of projected climate heating on wildlife populations, mechanistic tools are required to incorporate the inherent physiological effects of temperature changes, as well as the associated effects on food availability within and across comparable ecosystems. Here we applied an agent-based bioenergetics model to explore the combined effects of projected temperature increases for 2100 (1.4, 2.7, and 4.4°C), and associated changes in prey availability, on three-spined stickleback (Gasterosteus aculeatus) populations representing latitudes 50, 55, and 60°N. Our results showed a decline in population density after a simulated 1.4°C temperature increase at 50°N. In all other modeled scenarios there was an increase (inflation) in population density and biomass (per unit area) with climate heating, and this inflation increased with increasing latitude. We conclude that agent-based bioenergetics models are valuable tools in discerning the impacts of climate change on wild fish populations, which play important roles in aquatic food webs.

A structural perspective on the temperature-dependent activity of enzymes.

Enzymes are biomolecular catalysts whose activity varies with temperature. Unlike for small-molecule catalysts, the structural ensembles of enzymes can vary substantially with temperature, and it is in general unclear how this modulates the temperature dependence of activity. Here multi-temperature X-ray crystallography was used to record structural changes from -20°C to 40°C for a mesophilic enzyme in complex with inhibitors mimicking substrate-, intermediate-, and product-bound states, representative of major complexes underlying the kinetic constant . Both inhibitors, substrates and catalytically relevant loop motifs increasingly populate catalytically competent conformations as temperature increases. These changes occur even in temperature ranges where kinetic measurements show roughly linear Arrhenius/Eyring behavior where parameters characterizing the system are assumed to be temperature independent. Simple analysis shows that linear Arrhenius/Eyring behavior can still be observed when the underlying activation energy / enthalpy values vary with temperature, e.g., due to structural changes, and that the underlying thermodynamic parameters can be far from values derived from Arrhenius/Eyring model fits. Our results indicate a critical role for temperature-dependent atomic-resolution structural data in interpreting temperature-dependent kinetic data from enzymatic systems.

Unveiling thermally driven photoluminescence in CVD grown MoS[formula omitted] dendritic flake

High-quality MoS2 nanostructures were fabricated via chemical vapor deposition technique on SiO2/Si substrate. In this paper, the effect of temperature on the photoluminescence behavior of MoS2 dendritic flake is addressed. We scrutinized the photoluminescence spectra of monolayer and multilayer regions of MoS2 in the temperature range 300 K–680 K. Monolayer and multilayer behavior of MoS2 flakes are confirmed by Raman and Photoluminescence spectroscopy. The excitonic peaks from the multilayer regime become less intense and show a red shift compared to the monolayer PL spectra. Thermally-induced bandgap modulation of MoS2 is demonstrated. The excitonic intensity and peak positions reveal pronounced temperature-dependent changes. These changes are explicable through the increased electron–phonon interaction and lattice rearrangements. Furthermore, first principle calculations are employed to glean insight into the impact of atomic rearrangements on the band gap behavior of MoS2. Our research presents a detailed understanding of thermally driven band gap modulation of monolayer and multilayer MoS2, which is essential for designing optoelectronic devices.

Microwave-enhanced catalytic conversion of fatty acid ester to olefins by Na-ZSM-5

The bio-based production of essential chemicals is important for the sustainability of the chemical industry. Here, we demonstrate efficient olefin production from methyl oleate using Na substituted ZSM-5 (Na-ZSM-5) and microwave irradiation. Na-ZSM-5 exhibits superior microwave heating properties compared to H-ZSM-5 and other zeolites. It was more effective in converting methyl oleate to olefins such as ethylene and propylene than H-ZSM-5 or Y zeolites. Microwave irradiation promoted the conversion efficiency of methyl oleate by Na-ZSM-5, achieving an olefin yield over four times higher than that obtained with conventional heating (CH) using an electric furnace. Meanwhile, the aromatization to benzene, toluene and xylene (BTX) was suppressed using Na-ZSM-5, which was attributed to the removal of strong acid sites. In addition, in situ microwave XRD revealed that microwaves promoted temperature-dependent structural changes in Na-ZSM-5 at lower temperatures than CH, suggesting that microwaves form localized high temperatures in the zeolite. These localized high temperatures effectively enhance olefin production via microwave irradiation.

A Meshless Method of Radial Basis Function-Finite Difference Approach to 3-Dimensional Numerical Simulation on Selective Laser Melting Process

Selective laser melting (SLM) is a rapidly evolving technology that requires extensive knowledge and management for broader industrial adoption due to the complexity of phenomena involved. The selection of parameters and numerical analysis for the SLM process are both costly and time-consuming. In this paper, a three-dimensional radial basis function-finite difference (RBF-FD) meshless model is introduced to accurately and efficiently simulate the molten pool size and temperature distribution during the SLM process for austenitic stainless steel (AISI 316L). Two different volumetric moving heat source models were presented, namely the ray-tracing method heat source model and the double-ellipsoidal shape heat source model. The temperature-dependent material properties and phase change process were also considered, based on experiments and effective models. Results of the model for the molten pool size were validated with those of the literature. The proposed approach can be used to predict the effect of different laser power and scan speed on the molten pool size and temperature gradient along the depth direction. The result reveals that the depth of the molten pool is more sensitive to laser power than scan speed. Under the same scan speed, a 22% change in laser power (45 ± 10 W) affects the maximum temperature proportionally by about 9%. The developed algorithm is computationally efficient and suitable for industrial applications.

Abstract Mo131: Time-Restricted Feeding Normalizes Dim Light at Night-Induced Disruption of Cardiovascular Rhythms in Mice

Background: Light input to the suprachiasmatic nucleus entrains circadian rhythms in physiology and behavior to the day-night cycle. Exposure to light at night in people is associated with cardiometabolic disease. Pre-clinical studies show that artificial light at night, including at very low levels, disrupts day-night rhythms in activity, feeding behavior, heart rate, and blood pressure dipping. Hypothesis: Dim light at night (dLAN) disrupts day-night rhythms in feeding behavior to blunt day-night rhythms in autonomic input to the heart and blood pressure dipping. Methods: Mice (n=5-6/sex) in thermoneutral housing were implanted with telemetry probes to record heart rate, blood pressure, and core body temperature. Autonomic input to the heart was assessed by measuring heart rate and subtracting the temperature-dependent changes in the heart rate after pharmacological inhibition of muscarinic and β-adrenergic receptor activation. Mice were housed in 12 h light: 12 h dark cycles (LD, 200 lux: 0 lux) with ad libitum access to food (LD-ALF), subjected to 12 h light: 12 h dLAN cycles (dLAN-ALF; 200 lux: 5 lux) for two weeks, and then feeding was time-restricted (not calorically restricted) to the dLAN cycle (dLAN-RF). Data were extracted from Ponemah and Clocklab, and statistical analysis was done using GraphPad PRISM software. Results: Compared to LD-ALF mice, dLAN-ALF mice showed reduced amplitudes in day-night activity, feeding, heart rate, and blood pressure rhythms, with males more affected than females (p<0.001). dLAN-ALF male and female mice had decreased amplitudes in the day-night rhythms in autonomic input to the heart. In addition, dLAN-ALF male mice had less blood pressure dipping. dLAN-RF normalized autonomic input to the heart and heart rate in male and female mice (p<0.05, p<0.01, respectively). dLAN-RF also improved blood pressure dipping in male mice (p<0.001). dLAN-RF did not normalize activity rhythms. Conclusion: dLAN disrupts day-night rhythms in activity, feeding, heart rate, and blood pressure dipping in mice, with males being more impacted. Time-restricted feeding to the dLAN cycle normalizes autonomic input to the heart and blood pressure dipping. These data suggest that time-restricted feeding counteracts the light-at-night-induced circadian disruption of cardiovascular function.

Multi-mode up-conversion emission of Tm@Yb@Er phosphors for color modulation and thermometry

Rare earth doped up-conversion materials play an important role in information security, colorful display and temperature sensing. In this work, the up-conversion luminescence of NaYF4:0.2Tm/20Yb@NaYF4:20Yb@NaYF4:2Er/20Yb phosphors, synthesized by typical co-precipitation method, are investigated under different excitation condition. The emission color of sample can be tuned from yellow to blue-green through changing pump laser from 1550 to 980 nm because the Tm3+ ions in the core cannot be excited by 1550 nm laser. More interesting, the value of red-to-green (R/G) and blue-to-green (B/G) can be finely manipulated by tuning the excitation pulse width and frequency. This phenomenon can be interpreted by different rising processes of the green, red and blue up-conversion emission. In addition, the core-shell structured sample displays a temperature-dependent color change, ranging from blue-green to purple. The green emissions, radiated from thermal coupled levels (2H11/24S3/2), are used in thermometry and the max relatively sensing sensitivity reaches 0.01 K−1 at 303 K. The findings indicate that the core-shell Tm@Yb@Er phosphors, with excitation-dependent and temperature-dependent up-conversion luminescence, have potential applications in information security and temperature sensing.

Bending performance of parallel bamboo strand lumber under high-temperature treatment

ABSTRACT Parallel bamboo strand lumber (PBSL) is economical and environmentally friendly and has good mechanical properties, but as a combustible material, there is a lack of research on its bending performance at high temperatures. In this paper, specimens of moso-bamboo-based PBSL were prepared and three-point bending tests were conducted at 11 temperatures ranging from 20 to 270°C using a temperature-controlled box. It was observed that the modulus of rupture (MOR) and modulus of elasticity (MOE) were basically inversely proportional to the temperature. Meanwhile, the color changes, bending failure modes and load-displacement curves of PBSL at different temperatures were compiled. In addition, the mass loss of the specimens was calculated and the microstructure of PBSL was analyzed by electron microscopy scanning. The results showed that the high temperature had a significant effect on the moisture content of PBSL and its internal structure, which was manifested as the weakening of the MOR at the macroscopic level. Finally, the fitting equations for the temperature-dependent changes in MOR and MOE reduction factor of PBSL are proposed in this paper, which provide a reference for predicting the performance of PBSL components under high-temperature conditions.

Design of a Rotating Disk Electrode setup operating under high pressure and temperature: Application to CO2 reduction on gold

We describe the design and development of a rotating disk electrode (RDE) cell capable of operating at pressures up to 200 bar and temperatures up to 200 °C. This setup enables electrochemical surface characterization through techniques such as voltammetry and impedance spectroscopy, under different mass transport regimes. Furthermore, evaluation of catalytic performance, including CO2 reduction, is possible as the system works in a semi-continuous mode interfaced with online gas sample measurements. As a proof of concept of the high-pressure cell designed, we examined the temperature-dependent changes in the cyclic voltammograms (CVs) of polycrystalline gold up to 150 °C and 50 bar. Additionally, online catalytic performance of CO2 reduction to CO on a rotating polycrystalline gold disk electrode was investigated under different pressure and temperature. Our results indicate a positive impact of temperature on the faradaic efficiency (FE) towards CO up to 50 °C, beyond which a rapid drop in performance was observed at atmospheric pressure. Conversely, increasing pressure positively affected CO2 solubility in the electrolyte, resulting in enhanced FE towards CO, reaching approximately 90 % at 6 bar compared to 40 % at atmospheric pressure. Notably, further increases in pressure did not significantly alter the FE, but led to higher current densities. Moreover, at pressures exceeding 6 bar, we observed a plateau in efficiency at temperatures higher than 50 °C. This observation suggests that increasing pressure can sustain CO2 electrolysis, validating the hypothesis that increasing CO2 solubility would suppress catalytic decay at higher temperatures. This study opens up promising avenues for future investigations in electrocatalysis, ranging from fundamental explorations of surface modifications induced by variations in temperature and pressure to the development of high-performance catalysts.

Cation-induced morphological transitions and aggregation of thermoresponsive PNIPAM nanogels

Poly(N-isopropylacrylamide) (PNIPAM) nanogels are promising responsive colloidal particles that can be used in pharmaceutical applications as drug carriers. This work investigates the temperature-dependent morphological changes and agglomeration of PNIPAM nanogels in the presence of mono- and multi-valent cationic electrolytes. We described the deswelling, flocculation, thermal reversibility behaviour and aggregated morphology of PNIPAM nanogels over a range of electrolyte concentrations and temperatures revealing the critical transition points from stable suspension to spontaneous agglomeration. We demonstrated that the flocculating ability and the rate of aggregate formation follow the order of deswelling behaviour. Transmission electron microscopy and atomic force microscopy analysis revealed the presence of a shell-like layer with varying density in the multivalent electrolyte solutions when compared to those in aqueous medium. We identified a concentration threshold of the thermally induced reversible aggregation/dispersion for the PNIPAM nanogels in the presence of Na+ and K+ ions at 10 mM, for Mg2+ and Ca2+ ions at 1 mM and for Al3+ ions at 0.1 mM concentrations. Such concentration thresholds indicated the effective destabilization of the electrolyte system with multivalency following the Schulze–Hardy rule. Our findings were supported by applying a Debye screening model that accounts for the shielding effect of multivalent cationic electrolytes on these nanogel systems. Our experiments and the models confirmed the compression of the electric double layer as the valency and ionic strength increased, except for Al3+ at higher concentrations which seemed to disrupt the electrical double layer and cause reversal of zeta potential. Our work highlights the significant impact the presence of multivalent cations can impose on the stability and morphology of nanogels, and this understanding will help in designing responsive nanogel systems based on PNIPAM nanogels.