Salts Of Weak Acids Research Articles

Influence of weak acid salts and curing condition on supersulfated cement mortar

This study explores the impact of weak acid salt agents (citrate and tartrate) in the mixture and various curing conditions on the properties of supersulfated cement (SSC) mortar. Compressive strength tests were conducted on prism-shaped samples measuring 4 × 4 × 16 cm. A comprehensive analysis of the phase assemblage of hardened products was carried out using X-ray diffraction (XRD), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDS). The results reveal the abundant formation of ettringite (E) and hydrotalcite (Ht) when weak acid salt agents are added, especially in chloride and sulfate-rich curing solutions, leading to a notable increase in compressive strength, up to 200% compared to the control sample. Furthermore, the study demonstrates a substantial improvement in early and overall strength under temperature-stimulated curing conditions, accelerating the hydration reaction of SSC. These findings provide deeper insights into the factors influencing SSC hardening and strength development, offering valuable information for enhancing the efficiency and utilization of SSC in the construction industry, aligning with the goals of sustainable development.

Unexpected Supramolecular-Induced Redox Switching in Sandwich Gd Bisphthalocyaninate.

The redox state of the phthalocyanine in sandwich lanthanide complexes is crucial for their applications. In this work, we demonstrate that the cation-induced supramolecular assembly of crown-substituted phthalocyanine lanthanide complexes Ln[(15C5)4Pc]2 can be used to control the redox state of the ligand simultaneously with the coordination sphere of the central metal. We achieve unprecedented redox switching of phthalocyanine ligands in a double-decker Gd(III) complex, resulting from the intramolecular inclusion of potassium cations between the decks with simultaneous twisting of the ligands (the skew angle between them decreases from 44.61 to 0.21°). Such a structural change leads to an increase in the deck-to-deck distance and drastically facilitates ligand reduction. This process was shown to be anion-dependent: only potassium salts of weak acids (KOPiv and KOAc) induce intramolecular inclusion of cations with redox switching in contrast to salts of strong acids (KBr, KOPic, KSCN, and KPF6), where such a redox process does not occur. This breakthrough opens new avenues for controlling the electrochromic properties, of phthalocyanines, along with other properties, such as electrical conductivity, optics, etc.

Improved-sensitivity sodium citrate concentration sensor using modified thin-diameter polarization maintaining fiber

Sodium citrate, as strong alkali and weak acid salt, play an essential role in the food and pharmaceutical industries. However, lack of detection method selectivity, limited biocompatibility and complexity of the manufacturing process are challenges that hinder the practical application of the sensors. In this paper, a improved-sensitivity sodium citrate concentration sensor with simple and compact interrogation setup is proposed. The sensor is fabricated by fusion splicing the sandwich structure of modified thin-diameter polarization-maintaining fiber, two pieces of multimode fiber, and single-mode fiber. In theoretical modeling, the properties of the structure are investigated. In the experiment, the evanescent field generated by the modified thin-diameter polarization-maintaining fiber plays a vital role in the detection of different sodium citrate concentrations. The sodium citrate concentration sensor exhibits a high linear sensitivity response up to 4.65 nm/%. The sensor provided refractive index sensitivity of 3173.2 nm/RIU. In addition, the response, repeatability, and stability are also evaluated by the experiments. Our results show that the sodium citrate concentration sensor holds great promise for serving as a soft and biocompatible probe for monitoring sodium citrate in situ.

Experimental Investigation on Spontaneous Imbibition of Surfactant Mixtures in Low Permeability Reservoirs.

Spontaneous imbibition of surfactants could efficiently enhance oil recovery in low permeability sandstone reservoirs. The majority of studies have considered the application of individual surfactants to alter wettability and reduce interfacial tension (IFT). However, a significant synergistic effect has been reported between different types of surfactants and between salts and surfactants. Therefore, this study systematically studied the capability of a binary surfactant mixture (anionic/nonionic) and a ternary surfactant mixture (anionic/nonionic/strong base-weak acid salt) in imbibition enhanced oil recovery (IEOR). The interfacial properties and the cores' wettability were explored by IFT and contact angle measurements, respectively. Subsequently, the imbibition performances of different types of surfactant solutions were discussed. The results suggested that the surfactants' potential to enhance oil recovery followed the order of ternary surfactant mixture > binary surfactant mixture > anionic > nonionic > amphoteric > polymer. The ternary surfactant mixture exhibited strong capacity to reverse the rock surface from oil-wet (125°) to strongly water-wet (3°), which was more significant than both binary surfactant mixtures and individual surfactants. In addition, the ternary surfactant mixture led to an ultralow IFT value of 0.0015 mN/m, achieving the highest imbibition efficiency (45% OOIP). This research puts forward some new ideas on the application of the synergistic effects of surfactants in IEOR from low-permeability sandstone reservoirs.

The influence of different kinds of weak acid salts on the macro-performance, micro-structure, and hydration mechanism of the supersulfated cement

Supersulfated cement (SSC), mainly composed of solid wastes, is a highly promising low-carbon binding material, however, the application of SSC is still limited due to inherent defects in terms of strength and durability. In this paper, the influence of addition of different weak acid salts on the micro-structure and macro-performance of SSC has been investigated, and a pH-based mechanism for regulating the hydration process of supersulfated cement is proposed. The experimental results show that sodium lactate and low content of sodium citrate both promote the formation of hydration products AFt and C–S–H gel, which is beneficial to the improvement of frost resistance and the retention of strength in SSC. Furthermore, it is found that the dynamic adjustment of the pH value in the pore solution during the hydration process is a necessary condition for high performances of supersulfated cement, which can be realized by the weak acid salts. The high pH value in the early stage of hydration should be present to ensure the rapid dissolution of slag and gypsum, while the pH must be decreased to a certain value as the reaction proceeds, for the purpose of the stable growth of AFt. The mechanism interpreted here may pave the way for the mix optimization and broader application of SSC.

O AMBIENTE ESTUARINO E A VARIAÇÃO DE pH: LIMITES NATURAIS E OBSERVAÇÃO EXPERIMENTAL DO EFEITO DA ACIDIFICAÇÃO SOBRE A BIODISPONIBILIDADE DE FÓSFORO

THE ESTUARINE ENVIRONMENT AND pH VARIATION: NATURAL LIMTS AND EXPERIMENTAL OBSERVATION OF THE ACIDIFICATION EFFECT ON PHOSPHORUS BIOAVAILABILITY. This study shows the variation of pH in the Cananéia-Iguape Estuarine-Lagoon Complex (CIELC). Data from 3 years (2019, 2021, 2022) were obtained in 17 points presenting the following ranges: temperature (14.88-27.05 ºC), pH (7.16-8.40) and DIP (0.20-11.28 µmol L-1) along a saline gradient (0.05-32.09) under different hydrodynamics, biogeochemical processes and anthropogenic influence. The pH buffering capacity due to the presence of weak acid salts in saline water (S ≥ 30) was associated to the lowest DIP, decreasing with low salinity values, confirming the direct correlation among salinity and pH. The highest temperatures in the winter of 2021, corroborated with the abnormal climate event in that year. An in vitro experiment showed results of the interaction of PID and sediments with different textures, with and without the presence of the benthic microbiota under a considerable decreasing of the pH (acidification) in relation to the natural condition of this environment. The P sediment flux characterized Iguape sector as a P sink with or without biota, Ararapira sector as a P source with biota and Cananéia, as P source without biota. The salt water buffered the pH and sediment buffered DIP both associated to the biogeochemical and hydrodynamic processes contribute to the homeostasis in the system.

A state-of-the-art review on the liquid properties regarding energy and environmental performance in liquid desiccant air-conditioning systems

Liquid desiccant air-conditioning system (LDAS) becomes an attractive option for reducing the energy consumption of conventional air-conditioning systems. Despite lots of published papers on LDAS in various aspects, there is not yet a comprehensive and up-to-date review on the properties of liquid desiccants, while the selection of liquid desiccant plays essential role in the overall performance of LDAS. In this paper, a state-of-the-art review on the properties in regard of energy and environmental performance is delivered for present and potential liquid desiccants, including vapor–liquid equilibrium, specific heat capacity, safety concerns. The current situations and future concerns of liquid desiccant investigation can be obtained, while different kinds of liquid desiccant candidates can be compared and evaluated comprehensively. Existing liquid desiccant of halide salt faces severe drawback of corrosiveness in long-term use. Compared with existing liquid desiccants, the candidates of weak acid salt, ionic liquid and deep eutectic solvent behave low toxicity and friendly corrosiveness, whereas their weak moisture absorption ability, high cost or high viscosity is the bottleneck for further applications. Therefore, the mixture of them can be regarded as a promising candidate in LDAS applications, but the fundamental properties are urged to be measured. The work in this paper provides momentous reference and guidance for the exploration of new liquid desiccant as well as the evaluation of future prospect of LDAS.

Overcoming Bioavailability Challenges of Dasabuvir and Enabling a Triple-Combination Direct-Acting Antiviral HCV Regimen through a Salt of Very Weak Acid for Oral Delivery.

Dasabuvir is a non-nucleoside polymerase inhibitor for the treatment of hepatitis C virus (HCV) infection. It is an extremely weak diacidic drug (pKa = 8.2 and 9.2) and a prolific solvate former. Due to its exceedingly low aqueous solubility (≤0.127 μg/mL at pH 1-6.8, dose number of 1.31 × 104), crystalline dasabuvir free acid exhibited poor oral bioavailability in initial animal pharmacokinetic (PK) assessment. This necessitated the development of enabling formulation for human clinical studies to achieve the required therapeutic in vivo concentration of dasabuvir. While salt formation has been widely used to enhance the solubility and dissolution rate of solids, this approach has rarely been applied to develop oral solid dosage forms for acidic drugs as weak as dasabuvir due to concerns of rapid disproportionation and crystallization of its free acid. In this contribution, we detail our efforts in identifying dasabuvir monosodium monohydrate as a drug substance that is stable, manufacturable, and, most importantly, significantly enhances the dissolution and oral absorption of this poorly soluble drug. The oral delivery of dasabuvir through the salt approach has enabled the commercialization of the triple-combination direct-acting antiviral HCV regimen, Viekira Pak. The methodologies and solutions identified in targeted studies to overcome technical challenges encountered along the way (i.e., incorporation of polymers to inhibit crystallization and disproportionation and species mapping to enable salt manufacturing process, etc.) can be applied to other insoluble compounds.

Influence of Electroconvection on Chronopotentiograms of an Anion-Exchange Membrane in Solutions of Weak Polybasic Acid Salts.

Visualization of electroconvective (EC) vortices at the undulated surface of an AMX anion-exchange membrane (Astom, Osaka, Japan) was carried out in parallel with the measurement of chronopotentiograms. Weak polybasic acid salts, including 0.02 M solutions of tartaric (NaHT), phosphoric (NaH2PO4), and citric (NaH2Cit) acids salts, and NaCl were investigated. It was shown that, for a given current density normalized to the theoretical limiting current calculated by the Leveque equation (i/ilimtheor), EC vortex zone thickness, dEC, decreases in the order NaCl > NaHT > NaH2PO4 > NaH2Cit. This order is inverse to the increase in the intensity of proton generation in the membrane systems under study. The higher the intensity of proton generation, the lower the electroconvection. This is due to the fact that protons released into the depleted solution reduce the space charge density, which is the driver of EC. In all studied systems, a region in chronopotentiograms between the rapid growth of the potential drop and the attainment of its stationary values corresponds to the appearance of EC vortex clusters. The amplitude of the potential drop oscillations in the chronopotentiograms is proportional to the size of the observed vortex clusters.

Effect of pyrolysis temperature on Si release of alkali-enhanced Si-rich biochar and plant response

Recent studies have shown that silicon (Si) dissolution from biochar may be influenced by the pyrolysis temperature. In addition, the enhancement of biochar by treatment with alkali has been proposed to produce a Si source that can be used for environmentally friendly plant disease control. In this study, biochars from rice straw and rice husk pretreated with KOH, CaO and K2CO3 and then pyrolyzed at 350, 450 and 550 °C were prepared to evaluate the effects of pyrolysis temperature on Si release and plant uptake from alkali-enhanced Si-rich biochar. Extractable Si and dissolution Si from the prepared biochars were assessed by different short-term chemical methods and long-term (30-day) release in dilute acid and neutral salt solutions, respectively, along with a rice potting experiment in greenhouse. For both rice straw- and husk-derived alkali-enhanced biochars (RS-10KB and HS-10K2B, respectively), increasing the pyrolysis temperature from 350 to 550 °C generally had the highest extractable Si and increased Si content extracted by 5-day sodium carbonate and ammonium nitrate (5dSCAN) designated for fertilizer Si by 61–142%, whereas non-enhanced biochars had more extractable Si at 350 °C. The alkali-enhanced biochars produced at 550 °C pyrolysis temperature also released 82–172% and 27–79% more Si than that of 350 °C produced biochar in unbuffered weak acid and neutral salt solutions, respectively, over 30 days. In addition, alkali-enhanced biochars, especially that derived from rice husk at 550 °C facilitated 6–21% greater Si uptake by rice and 44–101% higher rice grain yields than lower temperature biochars, non-enhanced biochars, or conventional Si fertilizers (wollastonite and silicate calcium slag). Overall, this study demonstrated that 550 °C is more efficient than lower pyrolysis temperature for preparing alkali-enhanced biochar to improve Si release for plant growth.

Cold sintering zinc oxide with a crystalline zinc acetate dihydrate mass transport phase

Cold sintering of ZnO using crystalline zinc acetate dihydrate in the absence of added water is examined. Prior studies use an aqueous solvent, usually containing a weak acid, base, or organic salt, as the mass transport phase during cold sintering. This paper shows equivalent densification of ZnO using solid, powdered acetate as compared to previously mentioned aqueous-based transport phases. It also presents the potential to add zinc acetate in higher quantities without increasing the amount of total added transport phase, as solubility limits in aqueous solvents define the maximum amount of zinc acetate that can be added for a given volume of liquid. Experiments were conducted using the previously reported sinterometer, allowing for in situ experimental monitoring to show densification trends of this new transport phase as a function of concentration, time, and temperature. The potentially dramatic impacts of varying humidity during powder preparation on final sample density will also be discussed.

Barium concentration, phytoavailability, and risk assessment in soil-rice systems from an active barium mining region

Barium (Ba) is a non-essential and toxic element. In China, intensive Ba mining and Ba salt manufacturing have led to sharp increases in Ba in the environment, but little information is available regarding Ba concentrations in paddy soil and rice. The total concentrations and phytoavailability of Ba in paddy soils and paired rice samples collected from the world's largest Ba mine in Dahebian, Tianzhu, Guizhou Province, southwestern China, were investigated. Risk assessments of Ba exposure via rice consumption were also evaluated. The results indicated that extremely high Ba concentrations existed in paddy soils, ranging between 518 mg/kg and 65,760 mg/kg, which demonstrated severe Ba contamination, as expected. The concentrations of rice Ba varied from 0.10 to 3.5 mg/kg, and a significantly positive correlation (r = 0.51, p < 0.05) between rice Ba and water-extractable Ba was observed, suggesting that water, rather than weak acid (0.43 M CH3COOH), chelating agents (DTPA) or neutral salts (0.1 M NaNO3, 0.01 M CaCl2 or 1 M NH4OAc), is a suitable extractant for predicting the phytoavailable Ba in the studied soils. Risk assessments showed that residents experienced low Ba exposure via rice consumption when considered in isolation of other sources in this study area.

Mass production of low-boiling point solvent- and water-soluble graphene by simple salt-assisted ball milling.

Developing a mass production method for graphene is essential for practical usage of this remarkable material. Direct exfoliation of graphite in a liquid is a promising approach for production of high quality graphene. However, this technique has three huge obstacles to be solved; limitation of solvent, low yield and low quality (i.e., multilayer graphene with a small size). Here, we found that soluble graphite produced by mechanochemical reaction with salts overcomes the above three drawbacks. Soluble graphite was exfoliated into monolayer graphene with more than 10% yield in five minutes of sonication. The modified graphite was easily exfoliated in a low-boiling point solvent such as acetone, alcohol and water without the aid of a surfactant. Molecular simulation revealed that the salt is adsorbed to the active carbon at the graphite edge. In the case of weak acid salts, the original bonding nature between the alkali ion and the base molecule is retained after the reaction. Thus, alkali metals are easily dissociated in a polar solvent, leading to negative charge of graphene, enabling the exfoliation of graphite in low boiling point solvents. The approach proposed here opens up a new door to practical usage of the attractive 2D material.

Mechanochemical reaction using weak acid salts enables dispersion and exfoliation of nanomaterials in polar solvents

Nanomaterials, such as carbon nanotubes, graphene, and various types of nanosheets, form aggregates in dry powder due to attractive van der Walls forces. To bring out their unique properties, dispersion of the nanomaterial in solid or liquid is essential. However, the dispersion media for these materials are limited; the surface tension of liquid should be as close as possible to that of the nanomaterial. This limitation restricts the effective usage of nanomaterials. Here, we find that nanomaterials are easily dispersed or exfoliated in water and low-boiling point solvents after simple pretreatment. Pulverization of nanomaterials induces many dangling bonds at the newly created edge, and these active species react with weak acid salts. In polar solvent, the bonded salts are dissociated and enhance the negative charging of nanomaterials. The enhanced electric charging prevents the aggregation or restacking of nanosheets even in typically incompatible solvent such as water and alcohol. The functionalized powder can be easily exfoliated, giving more than 20% yield of nanosheets after only 5 min of sonication.

Direct exfoliation of layered materials in low-boiling point solvents using weak acid salts

The method for mass production of nanosheets is essential for fully realizing their commercial use. Direct exfoliation of layered materials in liquid is the simplest and low-cost technique for exfoliation without introducing defects in basal plane. However, the technique requires toxic and high-boiling point solvents, which makes it difficult for further processing. In addition, solvent exchange involves time-consuming processes such as filtering and redispersion. A breakthrough is necessary to make 2D-crystal-based functional dispersions. Here, we find a new method to directly exfoliate layered materials in low-boiling point solvents. Addition of small amounts of salt prevents reaggregation of exfoliated nanosheets and improves electrical repulsion. In this process, the mechanical force applied by sonication generates active carbon species at the fractured surfaces, leading to a reaction between the active carbon and the salt in liquid. High concentration graphene dispersions (1 g/L) can be obtained in isopropanol with only 5 min of sonication. We also confirm salt-assisted exfoliation is effective for the other 2D crystals such as MoS2 and boron nitride in a wide variety of polar solvents. Direct exfoliation in processable solution opens up a range of large-area applications such as high performance nanocomposites and coatings.

Effect of excipient properties, water activity, and water content on the disproportionation of a pharmaceutical salt

Excipients are crucial components of most pharmaceutical formulations. In the case of a solid oral dosage formulation containing the salt form of a weakly ionizable drug, excipient selection is critical, as some excipients are known to cause salt disproportionation (conversion of salt to the free form). Therefore, robust formulation design necessitates an in-depth understanding of the factors impacting salt disproportionation during processing or storage as this can negatively impact product quality and performance. To date, there is an incomplete understanding of key excipient properties influencing salt disproportionation. Specifically, the potential roles of amorphous excipient glass transition temperature and excipient hygroscopicity, if any, on salt disproportionation are still not well understood. Furthermore, the relationship between the compression and the extent of salt disproportionation is an unknown factor. Herein, by utilizing various grades of polyvinylpyrrolidone (PVP), its copolymer, copovidone (PVPVA), and magnesium stearate, a systematic investigation of disproportionation was performed using pioglitazone HCl as a model salt of a weak base. It was observed that there was a poor correlation between excipient hygroscopicity and the rate and extent of disproportionation. However, powder compression into compacts enhanced the rate and extent of disproportionation. This work focused on disproportionation of the salt of a weak base, as basic drugs are more prevalent, however, salts of weak acids may have similar tendencies under relevant conditions. The knowledge gained from this study will help in understanding the role of various excipients with respect to salt disproportionation, paving the way for designing stable salt formulations.

A Refined Developability Classification System

In 2010, the Developability Classification System (DCS) was proposed. The DCS was designed to close the gap between the biopharmaceutics classification system, which is aimed at guiding regulatory decisions about well-characterized drugs, and the need for early evaluation of drug candidates with respect to their suitability for oral delivery. The DCS applied solubility in fasted state simulated intestinal fluid to estimate intestinal solubility, assessed the compensatory nature of permeability and solubility during oral absorption and provided a way of estimating the critical the particle size at which dissolution becomes rate-limiting to absorption. Building on this framework, a refined developability classification system (rDCS) is now proposed. The rDCS is stratified into standard investigations applied to all candidates, and customized investigations. Standard investigation of solubility and permeability can be performed according to in-house methods, and the results compared with standard data sets of fasted state human intestinal fluid solubility and human effective jejunal permeability, which have been generated specifically for rDCS. Customized investigations are triggered when there is potential for supersaturation/precipitation (weak bases; salts of weak acids) and to assess dissolution versus permeation limited absorption. In addition, the rDCS offers facile visualization of the results, enabling pragmatic comparison of drug candidates and formulation approaches.

Salt-Induced Thermoresponsivity of Cross-Linked Polymethoxyethylaminophosphazene Hydrogels: Energetics of the Volume Phase Transition.

Biodegradable hydrogels of cross-linked polymethoxyethylaminophosphazenes (PMOEAPs) of various cross-linking density and apparent subchain hydrophobicity were investigated by high-sensitivity differential scanning calorimetry and equilibrium swelling measurements. The volume phase transition of the hydrogels was found to be induced by salts of weak polybasic acids. The transition parameters were determined depending on the pH, phosphate concentration, cross-linking density, and apparent hydrophobicity of the gels. The transition enthalpy increased three times and reached 60 J g-1 at the phosphate concentrations 5-100 mM. The transition temperature decreased by 60 °C when the pH changed from 6 to 8. A decrease in the transition temperature (by ∼20 °C) was achieved due to incorporation of 9.4 mol % of some alkyl groups into the gel subchains. The classic theory of the collapse of polymer gels coupled with the data of protein science on hydration energetics for various molecular surfaces reproduces correctly thermodynamics of the collapse of PMOEAP hydrogels.

Experimental study on performance of silica gel and potassium formate composite desiccant coated heat exchanger

In this paper, composite silica gel and potassium formate as typical organic weak acid salts is proposed to use in desiccant coated heat exchanger (DCHE). An experimental study on dynamic adsorption performance of desiccant coated metal sheet samples is conducted to obtain results with different proportions of silica gel and potassium format. A DCHE testing platform is then used to compare thermodynamic performance between single silica gel coated heat exchanger (SCHE) and composite potassium formate and silica gel coated heat exchanger (PSCHE). It is found that impregnating potassium formate into porous silica gel is an effective method to improve adsorption capacity, and 75% saturated potassium formate solution is recommended to constitute composite desiccant under experimental conditions. Compared with SG coated sheet, on average the maximum adsorption mass of SG&0.75PF coated sheet increases 2–3 times. Besides, PSCHE can obtain about 20% higher moisture removal capacity compared with SCHE under experimental condition, meaning the utilization of composite silica gel and potassium formate desiccant can effectively improve dehumidification capacity. PSCHE also can obtain 50% higher total cooling capacity compared with SCHE.

Effect of electro-activated solutions of sodium acetate and sodium propionate on geosmin producing Streptomyces avermitilis strain

Electro-activated solutions of salts of weak organic acids are defined as novel potent disinfecting agents that can be used in the agri-food industry. The aim of the present work is to study and understand the destruction mechanism of electro-activated solutions of sodium acetate (EAA) and sodium propionate (EAP) against Streptomyces avermitilis spores. The results of antibacterial activity showed high bacteriostatic effect for all the tested solutions, including sodium hypochlorite used as positive control. Under specific conditions, test on minimal inhibitory concentration demonstrated that the used electro-activated solutions have inhibition activity comparable or higher than the control solution, with the following inhibiting concentrations of 0.004, 0.002 and 0.073 mol/L, for EAA, EAP and NaOCl, respectively. The most active solutions resulted in destruction effect of more than 7 log CFU/mL. The physiological state of the S. avermitilis spores was assessed by transmission electron microscopy after treatments with the electro-activated organic solutions and NaOCl. The results displayed coreless and/or deformed cellular forms with ruptured membranes and released components of spores.The main practical importance of this study is that the targeted final objective is to develop safe and effective alternative to sodium hypochlorite to ensure microbial safety of fresh vegetables under storage conditions. In this context, we studied the potential of electro-activated solutions of sodium acetate and sodium propionate against spores of Streptomyces avermitilis and compared this activity with sodium hypochlorite, the mostly used disinfecting agent in the agri-food industry.