Physicochemical Processes Research Articles

A kinetic partitioning method for simulating the condensation mass flux of organic vapors in a wide volatility range

Organic aerosols are ubiquitous, playing important roles in various atmospheric physicochemical processes such as the formation of cloud droplets and haze. Condensation of organic vapors, as a net effect of association with particles and dissociation from the condensed phase, is a fundamental process that drives the formation of organic aerosols. Kinetic models are often used to simulate the condensation fluxes of low-volatility organic vapors and aerosol growth. However, the widely used kinetic growth models usually calculate the evaporation of a certain species based on previous particulate compositions, without including the co-condensation of other species. Here we present a new kinetic partitioning method for calculating the condensation fluxes of organic vapors in a wide volatility range with low computational cost. In this method, the organic vapors are assumed to be in a quasi-steady state, but never reach real association-dissociation equilibrium during the simultaneous condensation of multiple species. We show a good consistency between the kinetic partitioning method and kinetic models in simulating particle mass fractions and condensation fluxes. Under relevant atmospheric conditions, we reveal that the kinetic partitioning method also reproduce the trend that low-volatility species are almost non-volatile while volatile organic compounds almost reach association-dissociation equilibrium, while there is a transition regime between them. This transition regime varies with atmospheric conditions, such as temperature and vapor concentrations. Compared with previous studies combining kinetic growth methods with equilibrium partitioning theories to simplify the condensation flux calculation, this method helps to improve accuracy without a significant expense of computation cost, and it can be applied in a wider range of atmospheric conditions such as in extremely cold atmospheres and polluted exhaust plumes.

Two-phase flow visualization in direct ammonia fuel cells

In this work, the two-phase flow occurring in a direct ammonia fuel cell is visualized to understand the interactions between the complex physico-chemical processes involving in fuel cells. Experimental observations indicate that the appearance, growth, coalescence, detachment and sweeping processes of nitrogen bubbles occur periodically. Besides, the effect of operating conditions on the behavior of two-phase flow as well as cell performance is explored. Experimental results demonstrate that numerous nitrogen gas slugs are generated in the anode flow channel when the fuel flow rate is lower than 1.0 mL min−1, which seriously blocks the transport of NH3 and OH− to the anode catalyst layer. At an operating temperature of 95 °C, the flow channels are almost completely occupied by gases (a mixture of ammonia, nitrogen, and water), even under open-circuit conditions (a mixture of ammonia and water). In addition, the effects of using parallel and serpentine flow fields on the behaviour and flow patterns of two-phase flows are explored. Experimental results reveal that the parallel flow field is prone to clogging local flow channels by slugs. Moreover, the removal frequency of bubbles in the parallel design is significantly slower than that in the serpentine one.

Mechanisms of Action in FLASH Radiotherapy: A Comprehensive Review of Physicochemical and Biological Processes on Cancerous and Normal Cells.

The advent of FLASH radiotherapy (FLASH-RT) has brought forth a paradigm shift in cancer treatment, showcasing remarkable normal cell sparing effects with ultra-high dose rates (>40 Gy/s). This review delves into the multifaceted mechanisms underpinning the efficacy of FLASH effect, examining both physicochemical and biological hypotheses in cell biophysics. The physicochemical process encompasses oxygen depletion, reactive oxygen species, and free radical recombination. In parallel, the biological process explores the FLASH effect on the immune system and on blood vessels in treatment sites such as the brain, lung, gastrointestinal tract, skin, and subcutaneous tissue. This review investigated the selective targeting of cancer cells and the modulation of the tumor microenvironment through FLASH-RT. Examining these mechanisms, we explore the implications and challenges of integrating FLASH-RT into cancer treatment. The potential to spare normal cells, boost the immune response, and modify the tumor vasculature offers new therapeutic strategies. Despite progress in understanding FLASH-RT, this review highlights knowledge gaps, emphasizing the need for further research to optimize its clinical applications. The synthesis of physicochemical and biological insights serves as a comprehensive resource for cell biology, molecular biology, and biophysics researchers and clinicians navigating the evolution of FLASH-RT in cancer therapy.

Biochemical and immunomodulatory insights of extracellular matrix from decellularized human whole cervix: recellularization and in vivo ECM remodeling interplay

Extracellular matrix (ECM) rich whole organ bio-scaffolds, preserving structural integrity and essential growth factors, has potential towards regeneration and reconstruction. Women with cervical anomalies or trauma can benefit from clinical cervicovaginal repair using constructs rich in site specific ECM. In this study, complete human cervix decellularization was achieved using a modified perfusion-based stir bench top decellularization method. This was followed by physico-chemical processes including perfusion of ionic agents, enzymatic treatment and washing using detergent solutions for a duration of 10–12 d. Histopathological analysis, as well as DNA quantification confirmed the efficacy of the decellularization process. Tissue ultrastructure integrity was preserved and the same was validated via scanning electron microscopy and transmission electron microscopy studies. Biochemical analysis and structural characterizations like Fourier transform infrared, Raman spectroscopy of decellularized tissues demonstrated preservation of important proteins, crucial growth factors, collagen, and glycosaminoglycans. In vitro studies, using THP-1 and human umbilical vein endothelial cell (HUVEC) cells, demonstrated macrophage polarization from M1 to M2 and vascular functional genes enhancement, respectively, when treated with decellularized human cervical matrix (DHCp). Crosslinked DHC scaffolds were recellularized with site specific human cervical epithelial cells and HUVEC, showing non-cytotoxic cell viability and enhanced proliferation. Furthermore, DHC scaffolds showed immunomodulatory effects in vivo on small rodent model via upregulation of M2 macrophage genes as compared to decellularized rat cervix matrix scaffolds (DRC). DHC scaffolds underwent neo-vascularization followed by ECM remodeling with enhanced tissue integration.

Investigations on the Impact of a Series of Alkoxysilane Precursors on the Structure, Morphology and Wettability of an Established Zirconium-Modified Hybrid Anticorrosion Sol-Gel Coating.

The current study reports on the impact of a series of functional alkoxysilanes on the wettability and structure of a well-established silicon/zirconium hybrid anticorrosion sol-gel coating. The selected functional alkoxysilanes comprise tetra ethylorthosilicate (TEOS), 3-glycidyloxypropyltrimethoxysilane (GPTMS), 3-aminopropyltriethoxysilane (APTES) and vinyltriethoxysilane (VTES) and are incorporated at various concentrations (1, 5, 10 and 20%) within the silicon/zirconium sol-gel material. The prepared materials are successfully processed as coatings and cured at different temperatures in the range of 100-150 °C. The characterisation of the structures and surfaces is performed by dynamic light scattering (DLS), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), silicon nuclear magnetic resonance spectroscopy (29Si-NMR), atomic force microscopy (AFM) and static water contact angle (WCA). Structural characterisations (DLS, FTIR,29Si-NMR) show that the functional alkoxysilanes effectively bind at the surface of the reference sol-gel material, resulting in the formation of functional core-shell nanoparticles. WCA results show that the hydrophobic properties of all materials decrease with curing temperature, and AFM analysis demonstrated that this behaviour is associated with a decrease in roughness. The physico-chemical processes taking place are critically assigned and discussed.

Cassava starch modified montmorillonite - an efficient material for removal of crystal violet dye from contaminated aqueous solution

Because of grave effects on human health and the ecosystem, dye wastewater is exigent to be treated before its access to the environment. Removal of dyes from wastewater is one of the most important steps to eliminate its harmfulness. In this study, montmorillonite (MMT), a clay mineral with numerous applications in catalytic and coating purposes, was modified to form a new adsorbent for the removal of crystal violet (CV) dye from contaminated aqueous solution. Vietnamese cassava starch which is biodegradable, renewable, sustainable and affordable, was used as a modifier for MMT. The modified MMT was characterized by Fourier-transformed infrared (FT-IR) and X-ray diffraction (XRD) spectroscopic methods. Its morphology and structure were observed by Scanning electron microscopy (SEM). In addition, the effects of pH, interaction time, adsorbent concentration and temperature on the physico-chemical adsorption process on the basis surface of the material, have been investigated. Langmuir and Freundlich models were applied to analyze the adsorption values of dye solutions at the time of equilibrium. The results indicated that the modified MMT possessed the spherical shape, with particles on the surface in a wide size range. Investigation on the ideal removal conditions for modified MMT showed that it removed the crystal violet dye with maximum adsorption at pH value of 7 and concentration of 101.1 mg/g after 1 hour of interaction. Moreover, the Langmuir adsorption isotherm model was compatible with all results and the adsorption kinetics followed the pseudo-second-order model. Starch modified MMT should be promising for dye removal from wastewater.

Unravelling the effects of magmatic fractionation, fluid phase separation and dilution on the composition of magmatic-hydrothermal fluids of the Cornubian Batholith (SW England)

The compositional evolution of magmatic-hydrothermal fluids from the SnW mineralized Cornubian batholith was investigated via in situ fluid inclusion LA-ICP-MS microanalysis and reveals a large degree of variation between intrusive stages and at the sample scale, with complexities due to superposition of several mechanisms affecting fluids chemistry during the protracted evolution of the batholith. Despite large ranges of salinities (from <1 wt% to 48 wt% NaCleq.), the effects of individual processes such as magmatic differentiation, fluid saturation and boiling, fluid mixing and dilution can all be discerned on the basis of fluid inclusion trace element geochemistry combined with detailed petrography and microthermometry.In all samples, different fluid types (aqueous liquid-rich, vapor-rich and brine inclusions) were identified in variable proportions and microthermometry revealed complex temporal trends. Granite-related samples from the G5 intrusive stage are characterized by intermediate density fluids undergoing magmatic fractionation under pressure conditions above 1.5 kbar, indicated by successively decreasing fluid salinities with concomitant increases in Li, B, Rb and Cs concentrations. The latter two elements later strongly partitioned in the brine phase upon boiling, together with most of the other Cl-complexing elements (e.g., Fe, Mn, Pb, Zn). Those brines subsequently underwent progressive dilution with meteoric waters that caused a decrease in the concentration of all elements (besides B) and homogenization temperatures. In G3 granite from Dartmoor, on the other hand, brine inclusions represent the earliest fluid type while intermediate density fluids are absent, and a large salinity range in the fluid inclusion record associated with a decrease in homogenization temperatures represents their progressive dilution with meteoric fluid. The lack of intermediate density fluids at Dartmoor indicates fluid exsolution at relatively low pressures resulting in immediate phase separation into brine and vapor.All studied samples associated with ore mineralization display only the trend of dilution of high-salinity magmatic fluids. Their transition metal contents (e.g. Fe, Mn, Pb and Zn) show the expected positive correlation with salinity of the fluids. Conversely, the compositional trends observed for Sn and particularly W are more enigmatic, as they do not appear to significantly fractionate during most of the physicochemical processes outlined above and appear to be unrelated to fluid salinity, opposite of what would be expected for Sn as it is dominantly transported in Cl-complexes.This study highlights the key advantages of high-resolution geochemical fluid inclusion studies in discerning a variety of magmatic and post-magmatic processes in fluids in comparison to bulk fluid inclusion techniques or more simplistic fluid inclusions studies which might overlook important aspects of the typically complex history of fluids evolution in magmatic-hydrothermal systems.

Fire detection and suppression in rooms with different geometries

The paper presents experimental research findings on the integral characteristics of physicochemical processes in the area around a fire at different stages of its development and suppression. The purpose of this study was to determine the characteristics of the operation of fire detectors in rooms of various geometries. The temperatures in different cross sections, as well as the composition of gaseo us products of thermal decomposition and flame combustion of materials were investigated. The study dealt with class A fires involving wood. Mock-ups of rooms with distinctly different geometries were used: a parallelepiped, a rectangular truncated pyramid and a bow-roof (arched) structure. Efficient arrangement of technical equipment (light and gas analysis sensors, heat and smoke detectors, nozzles) was determined to provide early detection of a fire, prompt initiation of suppression and completion of combustion and smoldering. Minimum volumes of a firefighting liquid (water in this case) and spraying times were identified that are necessary and sufficient to suppress combustion. Guidelines were proposed on the arrangement of technical equipment for early fire detection and efficient containment of fire in the shortest time. A mathematical apparatus has been developed that allows predicting the performance of fire detectors and sensors. The research results can be used to evaluate the most effective locations for fire sensors in the design of buildings and structures.

Impedance spectroscopy applied to lithium battery materials: Good practices in measurements and analyses

This paper outlines a critical analysis of the currently available methodological framework for a comprehensive and reliable interpretation of impedance spectroscopy data of aprotic lithium-based secondary batteries. Impedance spectroscopy is a powerful experimental technique that can be used to assess the impedance of batteries over a range of frequencies. However, in typical battery configurations, all components contribute to the impedance response of the whole cell and the overlap of many of the different impedance responses often results in a complex experimental curve that is not easily easy to interpret. Various analytical approaches can be used to evaluate complex impedance data sets of batteries: (a) matching the impedance response of the cells in question with a previously published impedance model; (b) performing additional electrochemical measurements with different settings and/or on different cell designs to support the assignation of impedance contributions to specific physicochemical processes; (c) acquiring external physicochemical determinations, morphological and chemical data that can support or refute the results of impedance analysis; (d) developing theoretical models that reconcile physical insights at different length scales of the battery components with the equivalent circuit formalism.

Implementing a sustainable process for the recovery of palladium from spent catalysts at industrial scale: A LCA approach

Due to its unique physicochemical properties, palladium is widely used in several industry applications (e.g., vehicle emission control). In view of the circular economy, it is essential to explore secondary sources of palladium, such as urban mines. Current technologies for effective palladium recovery involve high energy consumption and severe environmental impact. More recently, a novel green method for recovering palladium from spent catalysts through a combination of mild acidic leaching and photodeposition on ZnO nanoparticles was proposed on a laboratory scale. In the present study, the environmental impacts of this recovery method, properly upscaled and modelled, was assessed by employing the LCA approach. Specifically, a comparative LCA was carried out for the process with as well as without recycling key components, such as Cu (II) and NaCl for the leaching solution and ZnO. The outcomes identified critical areas and drove the investigation of alternative process configurations to reduce its environmental footprint, such as the use of carbon dioxide in the photodeposition process with the aim of decreasing the resulting terrestrial ecotoxicity. This study marks a significant step forward in advancing research toward industrial−scale implementation of palladium recovery. It provides valuable insights for researchers in the field of green physicochemical processes for metal recovery, thus offering guidance for future decision−making towards more sustainable practices.

Complex Microlandscape as a Structural Unit of the Study of Spatiotemporal Development of an Ombrotrophic Suboceanic Bog

Ombrotrophic suboceanic bogs are distinguished by a high diversity of complex microlandscapes within the bog massif. Each complex microlandscape is a separate intrabog ecosystem with a specific set of parameters and relationships. This study aims to assess the specifics of the characteristics and parameters of the complex microlandscapes as part of an ombrotrophic suboceanic Sphagnum bog and as stages of bog morphogenesis, and to establish the internal relationships and their relationship with external environmental factors. A comprehensive multidisciplinary approach was used to assess the functioning of the complex microlandscapes. It was found that the relationship with the air temperature is closer than with the bog water table dynamics. It was shown that the morphometric parameters of perennial dwarf shrubs can serve as indicators of the stages of development of bogs. The processes of the self-regulation of complex microlandscapes are weakened with the age of the complex microlandscape, as evidenced by an increase in the amplitude of temperature fluctuations and the level of bog waters, as well as the key physicochemical parameters of the peat deposit. This leads to a gradual, slow reorientation of the physicochemical processes occurring in the deposit, from the deposition of organic matter to the decomposition of peat biomass.

Structural characterization of silver nanoparticles produced by biogenic synthesis using SAXS

Nanotechnology applied to the agricultural sector has highlighted in recent decades, making important contributions, including systems for pest control as biogenic nanoparticles. These nanoparticles are used to control phytopathogens, demonstrating the need to understand its composition, mechanisms of action and toxicity. Their capping of biomolecules, derived from the organism used in the synthesis, contributes to their stability and biological activity. Ag nanoparticles were produced by the fungus Trichoderma harzianum in aqueous solutions containing silver nitrate as a precursor for the silver nanoparticles. Some of the samples were exposed to the phytopathogenic fungus Sclerotinia sclerotiorum responsible for the white mold. After preparation, a fraction of the samples was submitted to physico-chemical processes to remove organic cap layer on nanoparticles surface formed during the preparation process. In this study we determined the effect of the phytopathogenic fungus and cap removal process in the average radius, radius dispersion, number density of the nanoparticles using small angle X-ray scattering (SAXS), where we considered their almost spherical shape in aqueous solution obtained by the biogenic route. The SAXS data analyses suggest that the presence of the pathogenic fungus results in a diminution of number and total volume of Ag NPs without significant effects on average radius and radius dispersion. Our results also indicate that the physic-chemical process to remove the organic cap surrounding the Ag NPs leads to a decrease in the fraction of the smaller nanoparticles.

Carbonated Water Injection for Enhanced Oil Recovery and CO2 Geosequestration in Different CO2 Repositories: A Review of Physicochemical Processes and Recent Advances

Carbonated Water Injection for Enhanced Oil Recovery and CO₂ Geosequestration in Different CO₂ Repositories: A Review of Physicochemical Processes and Recent Advances

Evaluation of Anti-urolithiasis Activity by Nucleation Assay

Many causes, including the efficiency of plant medicines and their lower side effects when compared to contemporary medications, have contributed to the current rebirth of plant therapies. Given the current situation, basic scientific research on the therapeutic herbs utilized in indigenous systems is urgently needed. The purpose of this review is to provide information on current developments in the study of medicinal plants recognized for their antiurolithiatic properties. This could assist researchers in determining and creating suitable lead compounds or plant products that are advantageous in the treatment of urolithiasis. A series of physicochemical processes, including supersaturation, nucleation, growth, aggregation, and retention inside the kidneys, combine to form kidney stones. In developed nations, 10–12% of people suffer from urinary stones. There are very few places in the world where stone disease is uncommon, such as Germany and the coastal regions of Japan. Thus, the purpose of this review is to provide information about current developments in the study of medicinal plants recognized for their antiurolithiatic properties. Researchers may find this article useful in identifying the primary compounds or herbal products that exhibit urolithiatic activity.

Biotransformation of free cyanide to formic acid by a cyanide hydratase−formamidase cascade reaction

Free cyanide (fCN) consisting of HCN and CN- is highly hazardous. Today, removal of cyanide from industrial (mining, plating, coke-plant) wastewaters largely relies on physicochemical processes followed by microbial degradation. Enzymatic processes are gaining ground but are still at a low technological stage. The cyanide-converting enzymes of interest are primarily cyanide dihydratases (CynDs; EC 3.5.5.1.), which hydrolyze HCN to formic acid and ammonia, and cyanide hydratases (CynHs; EC 4.2.1.66), which hydrate HCN to formamide. CynHs usually have much higher specific activities and a broader pH profile especially in the alkaline region compared to CynDs. However, the product of CynH, formamide, although much less toxic than fCN, still poses a significant health risk. Therefore, it is attractive to combine the CynH with an amidase that converts formamide to formic acid and ammonia. Here we demonstrate on a laboratory scale a two-step “one-pot” detoxification of fCN (5 mM) to formic acid using recombinantly produced purified enzymes − CynH from Exidia glandulosa and formamidase (EC 3.5.1.49) from Bacillus cereus. The reaction proceeds at pH 9.0–10.0, which reduces the risk of HCN escape. We also hypothesize that the cascade can be used for fCN determination after coupling an NAD-dependent formate dehydrogenase.

A systematic analysis and optimization of bicarbonate electrolysis based on a bipolar membrane through multiscale simulation

Bicarbonate electrolysis facilitated by bipolar membrane has emerged as a compelling alternative to gaseous CO2 electrolysis, primarily because of its enhanced product concentration and streamlined processes. However, despite increasing attention, a comprehensive understanding of bicarbonate electrolysis has been eclipsed by the complexity of the intertwined electrode reactions and water dissociation promotion mechanisms of bipolar membranes. A physics-based modeling approach has substantial potential to untangle the impact of intertwined physicochemical processes and expedite the optimization of bicarbonate electrolysis. In this study, a multiscale model coupled with a 1D bipolar membrane and a 2D cathode model is presented to explore the effects of bipolar membranes on cathode reactions and performance optimization using H+ flux as a bridge. For a bipolar membrane, the attenuation mechanism of water dissociation involving ohmic and concentration losses is presented and described using mathematical eqs. A quantification metric, the water dissociation efficiency of a bipolar membrane, is proposed to denote the degree of promoted water dissociation. Two noteworthy parameters related to the fixed functional group concentration are determined and detailed: the onset current density required to stimulate water dissociation and the limited water dissociation efficiency caused by attenuation. For the cathode, a synergistic enhancement mechanism among the operating parameters, membrane properties, and cathode properties is identified. The combined effect of these parameters on the electrolytic performance surpasses the sum of their individual enhancements. Following parameter optimization, there is a notable increase in the current density and Faraday efficiency of bicarbonate electrolysis by 68.6 mA/cm2 and 18.3%, respectively. This study provides a holistic understanding of bicarbonate electrolysis and substantial guidance for its future design.

Evaluation and Modeling of Polylactide Photodegradation under Ultraviolet Irradiation: Bio-Based Polyester Photolysis Mechanism.

In our study, we investigated the accelerated aging process of PLA under 253.7 nm UV-C irradiation with the use of the GPC, NMR, FTIR, and DSC methods and formal kinetic analysis. The results of GPC and DSC indicated a significant degree of destructive changes in the PLA macromolecules, while spectroscopic methods NMR and FTIR showed maintenance of the PLA main structural elements even after a long time of UV exposure. In addition to that, the GPC method displayed the formation of a high molecular weight fraction starting from 24 h of irradiation, and an increase in its content after 144 h of irradiation. It has been shown for the first time that a distinctive feature of prolonged UV exposure is the occurrence of intra- and intermolecular radical recombination reactions, leading to the formation of a high molecular weight fraction of PLA decomposition products. This causes the observed slowdown of the photolysis process. It was concluded that photolysis of PLA is a complex physicochemical process, the mechanism of which depends on morphological changes in the solid phase of the polymer under UV radiation.

Preparation of Ceramic Press Powder Based on Aluminosilicate Clay Raw Materials and Ash and Slag Waste from Thermal Power Plants Synthesized by Vitreous Microspheres

The possibility of using 3-component charges in the production of wall ceramics by semi-dry pressing from aluminosilicate loams in a composition with ash and slag waste from CHP plants, cullet and silica gel obtained by the sol-gel method is considered. The physicochemical processes and phase formations occurring in the production of ceramic materials using WCO at the firing stage have been studied. It was found that the introduction of fluxes in the form of cullet and silica gel reduces the temperature of heat treatment and are intensifiers of mineral neoplasms that increase mechanical strength compared with samples made from 2-component compositions «loam + ASW».

A 3-D Convolution-Based Burn-Through Point Multistep Prediction Model for Sintering Process

Predicting burn-through point (BTP) in advance is a quite critical task for the sintering process. However, sintering is a complex physicochemical reaction process, and the strong spatial-temporal correlations of data make the multi-step prediction task very challenging. The previous BTP multi-step prediction model only extracts spatial features in the high-level layers, leaving the spatial features in the low-level layers not learned. Specifically, the previous model only considers the relationships between the process variables and BTP, ignoring the spatial coupling relations among process variables. Further, the existing loss function is mainly based on Euclidean distance, which cannot learn dynamic information of multi-step prediction sequence. To tackle these problems, in this study, we propose a 3D convolution-based BTP multi-step prediction model (CBMP) to simultaneously capture spatial-temporal features. First, the 3D convolution is employed to capture the spatial-temporal features from low-level to high-level layers at the same time. Secondly, a spatial-temporal recalibration block is proposed to further refine the extracted features to increase the contributions of informative features and suppress the less useful ones. Finally, we design a time-aware multi-step prediction loss function to dynamically weigh the similarity between the actual sequence and the predicted sequence. The experimental results on two real-world BTP datasets demonstrate the effectiveness and feasibility of the proposed model on the BTP multi-step prediction task.

Use of synthetic calcium hydrosilicate in Portland cement compositions

We investigated the patterns of the synthesis of calcium hydrosilicate of tobermorite composition in the "amorphous silica–calcium hydroxide–water" system. The gradual interaction of calcium hydroxide and amorphous silicon(IV) oxide leading to the formation of synthetic tobermorite was confirmed by X-ray diffraction analysis. It was determined that the optimal duration of the synthesis of calcium hydrosilicate was 5 days, which, according to electron microscopic studies, ensured the production of grains with a size of 0.4–4 m. The influence of the synthesized tobermorite on the change in strength characteristics of cement stone during setting was studied using cement-sand mortar mixtures with sands of different particle size distribution. A comparative analysis of the effect of storage conditions of the synthesized product on the structure-forming processes of cement stone was carried out. It was established that the modifying effect of synthetic tobermorite was observed when it was dried after synthesis and stored in a dry state. Conversely, prolonged storage of calcium hydrosilicate in a wet state led to a loss of its activity and a decrease in the strength characteristics of cement stone. The mechanism of the influence of calcium hydrosilicate additive was studied by measuring the change in the rate of heat release of cement dough at the initial stage of hydration. It was shown that the addition of dry calcium hydrosilicate accelerated the physicochemical processes of hydration of clinker minerals, while the addition stored in wet conditions slowed down hydration. Electron microscopic studies of cement stone after 28 days of setting confirmed that the introduction of dry calcium hydrosilicate contributed to the formation of a structure characterized by a higher degree of crystallization and an increase in the strength of the samples.