Addition Of Salt Research Articles

Complete photodynamic inactivation of Pseudomonas aeruginosa biofilm with use of potassium iodide and its comparison with enzymatic pretreatment

Pseudomonas aeruginosa, a gram-negative bacterium, accounts for 7% of all hospital-acquired infections. Despite advances in medicine and antibiotic therapy, P. aeruginosa infection still results in high mortality rates of up to 62% in certain patient groups. This bacteria is also known to form biofilms, that are 10 to 1000 times more resistant to antibiotics compared to their free-floating counterparts. Photodynamic Inactivation (PDI) has been proved to be an effective antimicrobial technique for microbial control. This method involves the incubation of the pathogen with a photosensitizer (PS), then, a light at appropriated wavelength is applied, leading to the production of reactive oxygen species that are toxic to the microbial cells. Studies have focused on strategies to enhance the PDI efficacy, such as a pre-treatment with enzymes to degrade the biofilm matrix and/or an addition of inorganic salts to the PS. The aim of the present study is to evaluate the effectiveness of PDI against P. aeruginosa biofilm in association with the application of the enzymes prior to PDI (enzymatic pre-treatment) or the addition of potassium iodide (KI) to the photosensitizer solution, to increase the inactivation effectiveness of the treatment. First, a range of enzymes and PSs were tested, and the best protocols for combined treatments were selected. The results showed that the use of enzymes as a pre-treatment was effective to reduce the total biomass, however, when associated with PDI, mild bacterial reductions were obtained. Then, the use of KI in association with the PS was evaluated and the results showed that, PDI mediated by methylene blue (MB) in the presence of KI was able to completely eradicate the biofilm. However, when the PDI was performed with curcumin and KI, no additive reduction was observed. In conclusion, out of all strategies evaluated in the present study, the most promising strategy to improve PDI against P. aeruginosa biofilm was the use of KI in association with MB, resulting in eradication with 108 log bacterial inactivation.

Wastewater Treatment Using High-Performance In Situ Formed Double-Heterojunction Janus Photocatalyst Microparticles Shaped via a Microfluidic Device.

In this work, a heterogeneous photocatalysis system is fabricated for treating wastewater containing organic dyes and pharmaceutical substances. Double-heterojunction Janus photocatalysts are formed on the surface of size-tunable polydimethylsiloxane (PDMS) microparticles shaped via simple and low-cost coflow microfluidic devices. Ag0/Ag0-TiO2/TiO2 Janus-like photocatalysts are synthesized on the surface of porous PDMS microparticles as the support in which the metal-semiconductor heterojunction of Ag0/Ag0-TiO2 and the second heterojunction of Ag0-TiO2/TiO2 are created in situ, leading to the formation of Ag0/Ag0-TiO2/TiO2@PDMS photocatalysis systems. To form the heterojunctions on the PDMS surface, the polymer chain etching method is employed as a desired strategy to have half of the TiO2 nanoparticles on the surface of microparticles, which are treated by a Ag source. Using salt additives and the etching method, PDMS microparticles are made porous, providing more surface area for photoreactions. Surprisingly, the highest decomposition efficiencies of 94.4 and 91.1% are achieved for rhodamine B(RhB) and tetracycline (TC), respectively, under visible light for 60 min pH 11, a light source at a distance of 2 cm, 5 mM AgNO3, 10 wt % TiO2, 7 wt % NaCl, and 20 gm/L photocatalyst, which are conditions that result in the best performance for RhB degradation. Regarding the stability of the photocatalysts, no significant change is observed in the performance after five cycles.

Tuning the thermostability of GHG gels by salts at different positions on the Hofmeister scale

The influence of Hofmeister cations (NH4+, Na+, Mg2+) and anions (H2PO4−, CH3COO−, Cl−, NO3−) on the thermostability of a GHG hydrogel was investigated. The combined results of UV circular dichroism (UVCD) and Small Amplitude Oscillatory Shear Rheology experiments reveal that the addition of salt reduces the stability of the gel phase and the underlying fibrils. In line with the cationic Hofmeister hierarchy, the chaotropic Mg2+ ions caused the greatest thermal destabilization of the gel phase with the gel → sol transition temperature Tgs value lowered by 10 °C. In the absence of salt, the gel → sol transition probed by the storage modulus and microscopy is biphasic. In the presence of salt, it becomes monophasic. Contrary to expectations the presence of Hofmeister anions leads to a nearly identical reduction of the gel → sol transition temperatures. However, UVCD spectra suggest that they affect the ππ-stacking between imidazole groups to a different extent. We relate the absence of ion specificity regarding the solubility of fibrils (probed by UVCD) to the observed enthalpy-entropy compensation of the dissolution process. Our results combined show how CD spectroscopy and rheology combined yields a more nuanced picture of the processes underlying the gel → sol transition.

Addition of diazonium salts to the coordinatively unsaturated core of a dinuclear organoruthenium complex

Abstract The reaction of [Ru2(CO)4(µ-H)(µ-PtBu2)(µ-Ph2PCH2PPh2)] (1) with the diazonium salts [PhN2]BF4 and [p-BrC6H4N2]BF4 in dichloromethane at T = 273 K was investigated. The oxidative addition afforded the products [Ru2(CO)4(µ-H)(µ-PtBu2)(µ-Ph2PCH2PPh2)(µ-N2Ph)]BF4 (2a) and [Ru2(CO)4(µ-H)(µ-PtBu2)(µ-Ph2PCH2PPh2)(µ-N2C6H4-p-Br)]BF4 (2b) in good yields. The products have been characterized by NMR and IR spectroscopy and mass spectrometry and the molecular structure of 2a has been determined by a single-crystal X-ray diffraction analysis (monoclinic, space group P21/m, Z = 2).

Do Specific Ion Effects on Collective Relaxation Arise from Perturbation of Hydrogen-Bonding Network Structure?

The change in the transport properties (i.e., water diffusivity, shear viscosity, etc.) when adding salts to water has been used to classify ions as either being chaotropic or kosmotropic, a terminology based on the presumption that this phenomenon arises from respective breakdown or enhancement of the hydrogen-bonding network structure. Recent quasi-elastic neutron scattering measurements of the collective structural relaxation time, τC, in aqueous salt solutions were interpreted as confirming this proposed origin of ion effects on the dynamics of water. However, we find similar changes in τC in the same salt solutions based on molecular dynamics (MD) simulations using a coarse-grained water model in which no hydrogen bonding exists, challenging this conventional interpretation of mobility change resulting from the addition of salts to water. A thorough understanding of specific ion effects should be useful in diverse material manufacturing and biomedical applications, where these effects are prevalent, but poorly understood.

Unveiling the quality formation mechanism of hand-stretched dried noodle based on typical flour and processing technology

This study examined the physicochemical properties of flour determining hand-stretched dried noodles (HSDN) and the mechanisms involved. The findings indicated that the flexural performance, cooking and eating quality of HSDN was primarily influenced by gluten characteristics. Additionally, porosity was significantly impacted by the addition of salt, while selecting flour with a higher glutenin to gliadin ratio and lower damaged starch content could potentially reduce the amount of salt required, contributing to the pore structure of HSDN. The HSDN obtained from long-term resting processes demonstrated superior cooking and eating quality in comparison to short-term ones. The extended resting period facilitated the expulsion of trapped air within the dough and the relaxation of the gluten network, resulting in improved dispersal and orientation of excessively aggregated gluten proteins during the stretching process. This led to the formation of more protein branches and stable β-sheet structures during subsequent resting periods.

Salt assisted liquid-liquid extraction combined with dispersive liquid-liquid microextraction for the determination of 24 regulated polycyclic aromatic hydrocarbons in human serum

Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants of great concern due to their carcinogenicity and mutagenicity. Their determination in human serum, particularly in at-risk populations, is necessary but difficult because they are distributed over a wide range of polarity and are present at trace level. A new method combining salting-out assisted liquid-liquid extraction (SALLE) and dispersive liquid-liquid microextraction with solidification of floating organic drop (DLLME-SFO) adapted to a reduced volume of sample (100 µl) was developed to determine 24 PAHs in human serum. Some key parameters of DLLME-SFO (volume of extraction solvent, ratio of extraction/dispersive solvent volumes, and salt addition) were first studied by applying it to spiked pure water. For its application to serum, a sample treatment step involving SALLE was optimized in terms of nature and content of salts and applied upstream of DLLME-SFO. It was applied to the extraction of 24 regulated PAHs from spiked serum followed by an analysis by liquid chromatography coupled with UV and fluorescence detection. The extraction recoveries ranged from 48.2 and 116.0 % (relative standard deviations: 2.0–14.6 %, n=5–9), leading to limits of quantification of PAHs in human serum from 0.04 to 1.03 µg/L using fluorescence detection and from 10 to 40 µg/L using UV detection. This final method combining SALLE and DLLME-SFO showed numerous advantages such as no evaporation step, high efficiency and low solvent-consumption and will be useful for monitoring PAHs in low volumes of serum.

Histopathological Effects of Vitamin C and Common Salt Addition to Fish Water During Starvation in African Catfish, Clarias Gariepinus (Burchell, 1822)

Histopathological Effects of Vitamin C and Common Salt Addition to Fish Water During Starvation in African Catfish, Clarias Gariepinus (Burchell, 1822)

Comprehensive Analysis and Environmental Risk Assessment of Benzotriazoles in Airport Stormwater: A HS-SPME-GC × GC-TOF-MS-Based Procedure as a Tool for Sustainable Airport Runoff Water Management

Despite the numerous benefits of intensive air transport development, many activities associated with the operation of airports contribute to environmental pollution. The purpose of this research was the development, optimization, and validation of a headspace–solid-phase microextraction–comprehensive two-dimensional gas chromatography–time of flight–mass spectrometry (HS-SPME-GC × GC-TOF-MS)-based procedure for determining anti-corrosive compounds in airport stormwater. Optimized HS-SPME conditions include: 45 min extraction time, 100 °C temperature, 1.0 g salt addition, and 10 min desorption time at 270 °C. The developed procedure is sensitive, selective, accurate (recoveries ≥ 80.0%), and precise (the coefficient of variation (CV) ≤ 14.9%), making it a highly suitable tool for extensive airport stormwater quality monitoring. The validated analytical protocol was successfully used to detect pollutants, including 1H-BT, 4-MeBT, 5-MeBT, and 5,6-diMe-1H-BT, in stormwater from various European airports with different flight capacities. Throughout the sampling period at the investigated airports, 1H-benzotriazole was found in the highest concentrations, ranging from below the MQL to 467 mg/L. An ecotoxicological risk assessment revealed that 69% of the sites exhibited high risk levels (Risk Quotient ≥ 1). The developed procedure and carried out environmental risk assessments of benzotriazoles in airport stormwater enable an evidence-based approach to sustainable airport stormwater management.

Encapsulation films: Investigation into the degradation mechanism of multicomponent bio-based waterborne polyurethane in natural environments

In this study, the impact of different ratios of castor oil (CO) and polycarbonate diol (PCDL) mixed soft segments, as well as the introduction of sodium 2-[(2-aminoethyl)amino]ethanesulphonate (AAS-Na) salt, on the biodegradable waterborne polyurethane (WPU) was investigated. Firstly, various waterborne polyurethanes with different mixed soft segments were prepared by adjusting the ratios of castor oil and polycarbonate diol. Subsequently, varying amounts of AAS-Na salt were introduced to assess their influence on the polymer properties. The results indicated that the ratio of CO to PCDL significantly affected the mechanical properties and biodegradability of WPU. As the ratio decreased from 10:0 to 6:4, the tensile strength of WPU films decreased from 18 MPa to 11 MPa, while the elongation at break increased from 56 % to 258 %. Furthermore, the addition of AAS salt improved the water absorption and biodegradation rate of the material. When the ratio of CO to PCDL within the system is 10:0 and the molar content of AAS-Na is 20 mol%, the sample exhibits optimal water absorption of 132.12 % after 48 h and biodegradability of 30.58 % after 28 days. The degradation mechanism was preliminarily explored using Fourier-transform infrared spectroscopy. In conclusion, by adjusting the ratios of castor oil, polycarbonate diol, and AAS salt, a series of biodegradable waterborne polyurethanes with excellent performance were obtained. This study demonstrates the feasibility of developing biodegradable packaging materials using bio-based waterborne polyurethanes as the main component.

LC-HRMS-based metabolomics and lipidomics analyses of a novel probiotic Akkermansia Muciniphila in response to different nutritional stimulations

The mucin-degrading gut commensal Akkermansia muciniphila (A. muciniphila) negatively correlates with various diseases, including metabolic disorders, neurodegenerative disorders, and cancers, through interacting with host receptors by diverse molecules. Still, their exact metabolic capability within the nutrient-rich environment (such as in the human gut) is not fully characterized. Therefore, in the present study, we investigated the comprehensive metabolome and lipidome of A. muciniphila after supplementation of four major gut microbial nutrients: mucin, inorganic salts, bile salts, and short-chain fatty acids (SCFAs). Our results showed that mucin is the predominant driver of the different lipidomic and metabolomic profiles of A. muciniphila, and it promotes the overall growth of this bacteria. While the addition of inorganic salts, bile salts, and SCFAs was found to inhibit the growth of A. muciniphila. Interestingly, inorganic salts affected the purine metabolism in A. muciniphila cultures, while adding bile salts significantly increased the production of other bile acids and N-acyl amides. Lastly, SCFAs were identified to alter the A. muciniphila energy utilization of triglycerides, fatty acyls, and phosphatidylethanolamines. To our knowledge, this is the first study to examine the comprehensive lipidome and metabolome of A. muciniphila, which highlights the importance of nutritional impacts on the lipidome and metabolome of A. muciniphila and hence providing foundational knowledge to unveil the potential effects of A. muciniphila on host health.

Dipole Theory of Polyzwitterion Microgels and Gels.

The behavior of polyzwitterions, constituted by dipole-like zwitterionic monomers, is significantly different from that of uniformly charged polyelectrolytes. The origin of this difference lies in the intrinsic capacity of polyzwitterions to self-associate intramolecularly and associate with interpenetrating chains driven by dominant dipolar interactions. Earlier attempts to treat polyzwitterions implicitly assume that the dipoles of zwitterion monomers are randomly oriented. At ambient temperatures, the dipolar zwitterion monomers can readily align with each other generating quadrupoles and other multipoles and thus generating heterogeneous structures even in homogeneous solutions. Towards an attempt to understand the role of such dipolar associations, we present a mean field theory of solutions of polyzwitterions. Generally, we delineate a high-temperature regime where the zwitterion dipoles are randomly oriented from a low-temperature regime where quadrupole formation is significantly prevalent. We present closed-form formulas for: (1) Coil-globule transition in the low-temperature regime, the anti-polyelectrolyte effect of chain expansion upon addition of low molar mass salt, and chain relaxation times in dilute solutions. (2) Spontaneous formation of a mesomorphic state at the borderline between the high-temperature and low-temperature regimes and its characteristics. A universal law is presented for the radius of gyration of the microgel, as a proportionality to one-sixth power of the polymer concentration. (3) Swelling equilibrium of chemically cross-linked polyzwitterion gels in both the high temperature and low-temperature regimes. Addressing the hierarchical internal dynamics of polyzwitterion gels, we present a general stretched exponential law for the time-correlation function of gel displacement vector, that can be measured in dynamic light scattering experiments. The present theory is of direct experimental relevance and additional theoretical developments to all polyzwitterion systems, and generally to biological macromolecular systems such as intrinsically disordered proteins.

PHYSICOCHEMICAL PROPERTIES OF MOROCCAN OPUNTIA DILLENII FRUIT, EXTRACTION OF BETACYANINS AND STUDY OF ITS STABILITY AND ANTIOXIDANT ACTIVITY

The Opuntia dillenii (O. dillenii) belongs to the Cactaceae family and usually grows in arid and semi-arid zones worldwide. This succulent plant is known for its multiple health benefits and virtues. In practical terms, the current study aims to investigate the morphological and the physicochemical characteristics of Opuntia dillenii fruit collected from Morocco, as well as the determination of flavonoids, polyphenols and betacyanins contents in order to characterize, identify and facilitate the valorization of this species. The obtained results are compared with existing literature and thoroughly discussed. In addition, the pigment of betacyanins was extracted from the fruit pulp and characterized by UV-visible spectrophotometry. The study of the stablity of betacyanins was carried out in the presence of certain parameters such as the change of pH, temperature, light and the addition of salt. The antioxidant activity of the extracted betacyanins was further examined using the DPPH free radical scavenging assay and the total antioxidant capacity method.

Diffusiophoresis in Polymer and Nanoparticle Gradients.

Diffusiophoresis is the movement of the colloidal particles in response to a concentration gradient and can be observed for both electrolyte (e.g., salt) and nonelectrolyte (e.g., glucose) solutes. Here, we investigated the diffusiophoretic behavior of polystyrene (PS-carboxylate surface) microparticles in nonadsorbing charged and uncharged solute gradients [sodium polystyrenesulfonate (NaPSS), polyethylene glycol (PEG), and nanoscale colloidal silica (SiO2)] using a dead-end channel setup. We compared the diffusiophoretic motion in these gradient types with each other and to the case of using a monovalent salt gradient. In each of the nonadsorbing gradient systems (NaPSS, PEG, and SiO2 nanoparticles), the PS particles migrated toward the lower solute concentration. The exclusion distance values (from the initial position) of particles were recorded within the dead-end channel, and it was found that an increase in solute concentration increases exclusion from the main channel. In the polyelectrolyte case, the motion of PS microparticles was reduced by the addition of a background salt due to reduced electrostatic interaction, whereas it remained constant when using the neutral polymer. Particle diffusiophoresis in gradients of polyelectrolytes (charged macromolecules) is quite similar to the behavior when using a PEG gradient (uncharged macromolecule) in the presence of a background electrolyte. Moreover, we observed PS microparticles under different concentrations and molecular weights of PEG gradients. By combining the simulations, we estimated the exclusion length, which was previously proposed to be the order of the polymer radius. Furthermore, the movement of PS microparticles was analyzed in the gradient of silica nanoparticles. The exclusion distance was higher in silica nanoparticle gradients compared to similar-size PEG gradients because silica nanoparticles are charged. The diffusiophoretic transport of the PS microparticles could be simulated by considering the interaction between the PS microparticles and silica nanoparticles.

Effects of Salts on Helical Protoplast-Callose-Fiber Formation and Cell Division in Leaf Protoplast Culture of Arabidopsis thaliana: Ultrastructure of PCF Using Transmission Electron Microscopy

Effects of four salts addition (10-200 mM), NaCl, KCl, MgCl2, and CaCl2 were examined on the growth of protoplasts and formation of helical 1.5 mm long, protoplast-callose-fibers (PCF) in Arabidopsis thaliana liquid leaf protoplast cultures. The basal medium was Murashige and Skoog’s medium containing 1 μM 2,4-dichlorophenoxyacetic acid and 0.1 μM benzyladenine, 3% sucrose, and 0.4 M mannitol. The protoplast division was highly stimulated by the addition of 50 mM Ca2+ ion but was totally inhibited by 50 mM Mg2+ ion. Inhibition by K+ and Na+ ions was in-between. By contrast, PCF formation, whose numbers were counted under a fluorescence inverted microscope after Aniline Blue staining for β-1,3-glucan (callose), was stimulated by both K+ and Ca2+ ions but inhibited by Mg2+ ion. After selecting Arabidopsis PCF using a micromanipulator, the sub-fibril ultrastructure was examined by transmission electron microscopy (TEM). The PCFs of Betula platyphylla and Larix leptolepis, cultured with 200 mM Ca2+ and 50 mM Mg2+ ions, respectively, after long-term storage and rehydration, were examined by TEM. The effects of different factors were discussed on PCF formation and sub-structures in different herbaceous and tree plant species.

Cover Feature: Enabling the Use of Lithium Bis(trifluoromethanesulfonyl)imide as Electrolyte Salt for Li‐Ion Batteries Based on Silicon Anodes and Li(Ni0.4Co0.4Mn0.2)O2 Cathodes by Salt Additives (Batteries & Supercaps 6/2024)

Cover Feature: Enabling the Use of Lithium Bis(trifluoromethanesulfonyl)imide as Electrolyte Salt for Li‐Ion Batteries Based on Silicon Anodes and Li(Ni_0.4Co_0.4Mn_0.2)O₂ Cathodes by Salt Additives (Batteries & Supercaps 6/2024)

A Label-Free Colorimetric AuNP-Aptasensor for the Rapid Detection of Vibrio cholerae O139.

Waterborne pathogens pose a significant threat to public health, emphasizing the continuous necessity for advancing robust detection techniques, particularly in preventing outbreaks associated with these pathogens. This study focuses on cholera, an infectious disease caused by Vibrio cholerae, serogroups O1 and O139, often transmitted through contaminated water and food, raising significant public health concerns in areas with poor sanitation and limited access to clean water. We developed a colorimetric biosensor using aptamer-functionalized gold nanoparticles to identify Vibrio cholerae O139 and address this issue. The detection mechanism relies on the color change of gold nanoparticles (AuNPs) from red to blue-purple induced by NaCl after the pathogen incubation and aptamer-target binding. Initial steps involved synthesizing and characterizing AuNPs, then exploring the impact of aptamer and NaCl concentrations on AuNP agglomeration. Optimization procedures for aptamer concentration and salt addition identified the optimal conditions for detection as 120 pM aptamers and 1 M NaCl. The aptasensor demonstrated a robust linear relationship, detecting V. cholerae concentrations from 103 to 108 CFU/mL, with a limit of detection (LOD) of 587 CFU/mL. Specificity tests and accurate sample analyses confirmed the efficiency of the AuNPs aptasensor, showcasing its reliability and speed compared to traditional culture examination methods. Moreover, we extended the aptasensor to a paper-based sensing platform with similar detection principles. The change in color upon target binding was captured with a smartphone and analyzed using image processing software. The paper-based device detected the target in less than 2 min, demonstrating its convenience for on-field applications.

Ultrasound Microwave Assisted Extraction Pada Daun Serai Wangi Menggunakan Pelarut Ionik.

Leaves of citronella (Cymbopogon nardus L.) have pretty much essential oil. Essential oil from citronella leaves is generally extracted by conventional methods. Conventional method is still less effective. The problem can be overcome by using non-conventional methods in the form of UMAE (Ultrasound-Microwave Assisted Extraction). UMAE is an extraction process assisted by ultrasound and microwaves. NaCl solution can be used as a solvent in the UMAE method because NaCl has a large dielectric constant. The aim of this study was to examine the effect of extraction time and the addition of salt on the yield and color of essential oils produced using the UMAE. The extraction process begins with the raw material preparation stage, such as harvesting, size reduction, and drying. Then, pre-treatment was carried out using ultrasound for 5 minutes at 35oC with the addition of 2, 4, 6, 8, and 10% (w/v) salt. Pre-treatment results were followed by the extraction process using microwaves for 30, 45, 60, 75, and 90 minutes. The best results were obtained with the addition of 6% salt and 60 minutes of extraction time with a feed to solvent ratio of 0.1 with a yield of 1.975% and the color is yellow.

Effects of Salt Content and Freeze-Thaw Conditions on Dynamic characteristics and its microscopic mechanism of Chloride Silty Clay

Generally, artificial ground freezing (AGF) technology is utilized to guarantee tunnel safety during construction. However, the soil structure changes significantly after freeze-thaw, resulting in uneven deformation of the tunnel under traffic loading from subway vibration. To solve this problem effectively, it is necessary to consider the combined impact of freeze-thaw, salt, and traffic loading damage that marine soft soil must withstand simultaneously. For this reason, cyclic triaxial test and NMR test were performed on the silty clay saturated with NaCl solution in this study. The influence of three main factors on dynamic properties has been thoroughly investigated, namely freeze-thaw, salt content, and confining pressure. According to cyclic triaxial test, the shape of the hysteresis loop of the specimens after freeze-thaw changed more significantly with increasing loading cycles. The dynamic elastic modulus was weakened by freeze-thaw, while improved by the addition of NaCl. Damping ratio was consistent with the dynamic elastic modulus law. It was worth noting that the different freezing temperatures (−10 °C, −20 °C and − 30 °C) had only a slight impact on dynamic elastic modulus, as well as damping ratio. Mathematical models were proposed to forecast the dynamic elastic modulus and damping ratio regarding marine soft clay. NMR test indicated that the addition of salt made the internal pore environment of the specimens tend to be consistent and enhanced the water-solid interaction. The increase in porosity resulted in the decrease in dynamic elastic modulus. The results have provided valuable insights into the mechanical characteristics of marine soft clay when AGF technology is applied.

Enhanced electroactive β‐phase and dielectric properties in P(VDF‐HFP) composite flexible films through doping with three calcium chloride salts: CaCl2, CaCl2·2H2O, and CaCl2·6H2O

AbstractFlexible dielectric films with a high dielectric constant, utilizing P(VDF‐HFP)/salt composites, were manufactured through the solution casting method. In this work, we studied the impacts of three calcium chloride salts—CaCl2, CaCl2·2H2O, and CaCl2·6H2O—on the surface morphology, crystalline phase transformation, mechanical properties, and dielectric responses of the P(VDF‐HFP) copolymer. The detailed structure and properties of all samples were assessed via scanning electron microscope (SEM), atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), tensile testing, and LCR meter analysis. The experimental results demonstrated that the addition of calcium salts to the P(VDF‐HFP) composites induced a visibly microporous morphology, with the porosity and surface roughness of the composites gradually increasing with salt content. In comparison to the pure P(VDF‐HFP) film, the composite films exhibited decreased stiffness and heightened flexibility. Furthermore, a higher β‐phase fraction and notable enhancements in the dielectric constant resulting from the inclusion of calcium salts were observed. Consequently, the P(VDF‐HFP) composite filled with 3 wt% of CaCl2·6H2O demonstrated the highest capability for promoting the β‐phase fraction and dielectric constant, achieving values of 98.33% and 21.49% (at 10 Hz), respectively.