Sulfuric Acid Research Articles

Recycling B4C grinding waste to fabricate high-performance ceramics by modification treatments and hot pressing

B4C grinding waste, originated from the fine grinding process of sapphire wafers, is discarded without reutilization, which causes environmental pollution and resource waste. This work proposes new methods on recycling B4C grinding waste to fabricate high-performance ceramics by first modification treatments via ball-milling mixing or microwave digestion with sulfuric acid and then hot pressing. The characteristic of B4C grinding waste is studied and Al2O3 is the main impurity. The direct hot pressing of B4C grinding waste is performed and the obtained ceramic is fragile. The large-size and unevenly distributed Al2O3 is verified to cause the fracture according to the structure analysis. Ball-milling mixing can break the Al2O3 agglomerate and make Al2O3 distribute evenly, and microwave digestion with sulfuric acid can remove most Al2O3. The ceramics fabricated via hot pressing with B4C grinding waste treated with ball-milling mixing or microwave digestion show good microstructure and mechanical property. The relative density, hardness, flexural strength and fracture toughness of the ceramics fabricated with grinding waste treated with ball-milling mixing are 98.82%, 32.42 GPa, 439.44 MPa, 4.82 MPam1/2, respectively, higher than those of the ceramics fabricated with grinding waste treated with microwave digestion, which are 98.69%, 29.54 GPa, 368.18 MPa, 4.20 MPam1/2, respectively. This work not only realizes the secondary utilization of waste and avoids pollution, but also provides another way supplying the high-cost B4C powder and ceramic, which has high economic benefits.

Carbon dots with high brightness and stability towards efficient Cr(Ⅵ) and l-arginine sensors

To create fluorescent sensors for Cr (VI) and l-arginine detection, blue-emitting carbon dots (CDs, named as M-CDs) were prepared via a solvothermal synthesis by using m-phenylenediamine. The introduction of sulfuric acid changed the blue-emitting of CDs into green-emitting (named as S-CDs), in which the photoluminescence (PL) peak wavelengths of samples M-CDs and S-CDs were 450 and 540 nm, while their PL efficiencies were 21.7 and 84.2 % respectively. Sulfuric acid resulted in the average fluorescent lifetime of the CDs was prolonged into 8.19 from 4.65 ns. The photo and thermal stable tests demonstrated that theses CDs revealed excellent stability. Meanwhile, CDs flexible films with bright blue- and green-emitting were prepared utilizing the favorable solubility of CDs in polar solvents. Mono-dispersed CDs as luminescent materials demonstrated it promising prospects in luminescent devices field. Furthermore, M-CDs exhibited excellent selectivity towards Cr(Ⅵ) and l-arginine. The detected limit (0.86 μM for Cr(Ⅵ) and 0.43 μM for l-arginine) was determined by assessing the response of M-CDs to various concentrations of Cr(Ⅵ) ion and l-arginine solutions. These bright CDs revealed great potential for accurate detection of Cr(Ⅵ) and l-arginine.

Synergistic extraction of zinc from spent acid using P507-P204: A novel approach for efficient separation

A novel system for the synergistic extraction of zinc from spent acid using a mixture of 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester (P507) and Di-2-ethylhexyl phosphoric acid (P204) as extractant is proposed. The optimum extraction parameters of P507-P204 are investigated, and the results exhibit that 84.80% of zinc is extracted at a solution pH control of 1, the V(P507):V(P204) of 4:1, the P507-P204 concentration of 30% (v/v), and the phase ratio (O/A) of 2:1. Furthermore, the zinc can be effectively stripped from its extracted complex by sulfuric acid. The synergistic extraction mechanism of P507-P204 is identified by slope analysis, FT-IR, mass spectrum, and 31P-NMR. In addition, the mechanism of synergistic extraction of zinc by P507-P204 is cation exchange and releases two hydrogen ions during zinc extraction. In a word, the establishment of this synergistic system realizes the effective separation of zinc from spent acid and has potential industrial application value.

Investigating the environmental impacts of lithium-oxygen battery cathode production: A comprehensive assessment of the effects associated with oxygen cathode manufacturing

Lithium-oxygen batteries offer remarkably high energy density compared to current lithium-ion batteries. The key to their electrochemical performance lies in the processes occurring at the air cathode. However, the complexity of these reactions, coupled with the by-products generated during discharge, can make the reaction process slow or impede their efficiency. This study evaluates the environmental impact of high-efficiency lithium-oxygen batteries cathodes, including titanium oxide composites, graphene-based composites and activated carbon-based composites, through a life cycle assessment across 18 impact categories using a cradle-to-gate approach with a functional unit of 25 kWh. Results show that active material production was the largest contributor to environmental impact, particularly Global Warming Potential. Among the evaluated cathodes, reduced graphene oxide/α-mnaganese oxide/palladium (rGO/α-MnO2/Pd) demonstrated the highest environmental impact, with a global warming potential of 1130.71 kg carbon dioxide from active material production, due to its energy-intensive synthesis and the use of chemicals like sulfuric acid, sodium borohydride, hydrochloric acid, and hydrogen peroxide. Additionally, the rGO/α-MnO2/Pd cathode had the highest Human Toxicity Potential and Ozone Depletion Potential. Batteries with graphene-based cathodes achieved a specific capacity of 7500 mAh.g-1, underscoring their performance potential while highlighting the need for more sustainable cathode manufacturing methods. These findings emphasize the environmental considerations necessary for large-scale lithium-oxygen batteries implementation.

Cyanobacterial hydrothermal carbonization carbon as photocatalyst for selective aerobic oxidation of cyclohexane

The exploration of catalyst preparation techniques that incorporate environmental-friendly methodologies has consistently been the focus of scientific inquiry within the field of green synthesis of oxygen-containing organic chemicals. Herein, a metal-free hydrothermal carbonation carbon (HTCC) has been prepared utilizing cyanobacterial biomass produced during a water bloom in a freshwater lake. The HTCC produced is capable of performing photocatalytic selective oxidation of cyclohexane to cyclohexanol and cyclohexanone (KA oil) under ambient conditions. The use of cyanobacterial biomass allows for the efficient preparation of HTCC, which exhibits a conversion rate of cyclohexane that is 4.1 times of HTCC prepared with alternative carbon sources (glucose). The selectivity to KA oil over the samples are almost 100%. Characterizations and analysis reveal that cyanobacteria can lead to self-doping of nitrogen and hydrophobicity of the resulting HTCC, while sulfuric acid etching endow it with more photoactive sp2 hybridized structure units that contribute to a higher photogenerated carrier separation efficiency. The suitable band structure enables the cyanobacterial HTCC to produce superoxide radicals to oxidize cyclohexane. These findings are of great significance for the development of eco-friendly photocatalysts and the utilization of biomass resources.

High-efficiency leaching process for selective leaching of lithium from spent lithium iron phosphate

With the arrival of the scrapping wave of lithium iron phosphate (LiFePO4) batteries, a green and effective solution for recycling these waste batteries is urgently required. Reasonable recycling of spent LiFePO4 (SLFP) batteries is critical for resource recovery and environmental preservation. In this study, mild and efficient, highly selective leaching of lithium from spent lithium iron phosphate was achieved using potassium pyrosulfate (K2S2O7) and hydrogen peroxide (H2O2) as leaching agents. The leaching rates of lithium and iron were 99.83 % and 0.34 %, respectively, at the optimal leaching conditions of 4 vol% 30 wt% H2O2, 0.08 mol/L K2S2O7, 25℃, 5 min, and a solid–liquid ratio of 20 g/L. Meanwhile, the mechanism of the leaching process was explored by thermodynamic, XRD, XPS, FTIR, and SEM analyses. The leaching solution was concentrated and purified, with the addition of potassium carbonate (K2CO3) to convert lithium into lithium carbonate (Li2CO3). A small amount of sulfuric acid (H2SO4) is added to the saline wastewater after precipitation, which can be converted into a leaching agent for recycling after heat treatment. This study provides a sustainable green process for the recovery of lithium iron phosphate and a new idea for resource recovery.

Enhanced decoupling of conductivity relaxation from structural relaxation in non-stoichiometric protic ionic liquids involving triflic acid and 2-aminoethyl hydrogen sulfate.

The glass transition dynamics and conductivity relaxation are studied for a series of non-stoichiometric protic ionic liquids (PILs) based on 2-aminoethyl hydrogen sulfate and triflic acid with varying molar ratios (denoted as AT-55, AT-46, AT-37, AT-28, and AT-19) by broadband dielectric spectroscopy in a wide frequency (10-1-107Hz) and temperature range (173-353K). The results indicate that the addition of acid lowers the glass transition temperature, as confirmed by the activation energy fine structure analysis and a crossover in the conductivity relaxation time. Notably, samples with higher acid content deliver markedly increased conductivity. In addition, detailed analysis of the permittivity and modulus spectra reveals enhanced decoupling between the structural (α-process) and conductivity relaxation in samples with a higher acid content. Remarkably, nano-phase separation in AT-28 and AT-19 samples is observed, resulting in a second glass transition temperature indicating a more mobile phase. Based on the above-mentioned findings, we infer that increased acid content disrupts strong ionic interactions within the IL fraction, resulting in a decrease in the glass transition temperature and leading to nano-phase separation into distinct acid-rich and IL-rich phases with varying Tg values. This phase separation alters the long-range ionic pathways, shifting from being solely governed by IL cluster dynamics to a scenario where charge transport becomes largely decoupled from the dynamics of IL-rich clusters. Hence, modulating the stoichiometry of PILs appears a promising approach to enhance the conductivity together with widening the usable temperature range for applications.

Sulfuric acid effects in seed dormancy break of Ipomoea batatas evaluated by enzymatic, anatomic and physiological approaches

ABSTRACT The recommended method to overcome seed coat dormancy in sweet potato seeds is exposure to sulfuric acid, which can damage the embryo and affect seedling development depending on exposure time. This study aimed to determine the ideal immersion period using physiological, anatomical, and enzymatic analyses. Seeds were scarified with concentrated sulfuric acid for nine immersion periods. Physiological analyses included germination tests, germination speed index, first germination count, emergence test, and emergence speed index. Image analysis quantified the primary root length, root-to-hypocotyl ratio, and seedling length. Catalase and superoxide dismutase enzyme activities were analysed. Seed coat anatomy, including thickness, wear, and colour, was also assessed. Exposure to sulfuric acid for 30 min effectively broke dormancy without impacting the antioxidant system or seedling development. Thermal chambers confirmed that chemically scarified seeds absorb water and activate metabolism faster. Plant anatomy helped illustrate how sulfuric acid breaks dormancy by eroding physical barriers.

Molecular Mechanisms of Aerosol Nucleation: from CLOUD Chamber Experiments to Field Observations

Atmospheric aerosol particles contribute to over four million premature deaths annually and play a critical role in modulating Earth’s climate. Most atmospheric particles and more than 50% of the cloud condensation nuclei are formed through a secondary process named new particle formation involving unique precursor vapors. This article summarizes current knowledge of how new atmospheric particles form, based on experiments at the CERN CLOUD chamber. While the role of sulfuric acid has long been known, other vapors like highly oxygenated organic molecules and iodine oxoacids are also important, along with stabilizers like ammonia, amines, and ions from cosmic rays. We explain how findings from CLOUD experiments help us understand particle formation in various atmospheric conditions and improve air quality and climate models.

High Proton Conductivity of Acid Impregnated COFs Stabilized by Post-Oxidation.

The investigation of proton conduction processes within artificial nanopores using phosphoric acid (H3PO4) and sulfuric acid (H2SO4) not only sheds light on the mechanisms of proton conduction for these strong acids in confined environments, while also provides critical insights into the proper understanding of biological transmembrane proton transport. However, the synthesis of stable and acid-resistant host frameworks is yet a major challenges. By following that, the present study is conducted with the aim of improving the chemical stability of an imine-based COF (CPOF-10) by converting it into an amide-linked COF (CPOF-11) via a post-oxidative approach. In which, the integration of an appropriate amount of imidazole groups into the framework facilitates the efficient impregnation of liquid proton-conducting acids. The obtained results indicate the ten times greater proton conductivity of H3PO4@CPOF-11 than that of H3PO4@CPOF-10, thereby, successfully achieving 8.63 × 10-2 S cm-1 at 160°C, under nitrogen (N2) atmosphere. Moreover, the highly stable CPOF-11 tolerated H2SO4 doping, delivering a high proton conductivity of up to 1.70 × 10-1 S cm-1 at 140°C, with a significantly low activation energy of 0.05 eV. To the best of the knowledge, this activation energy (0.05 eV) of H2SO4@CPOF-11 is found to be one of the lowest value among all the reported proton-conducting materials. Thus, this study will provide new understanding for the fabrication of advanced porous organic materials in fuel cells application.

Effect of Nature and Charge of Counterions and Co-Ions on Electrotransport Properties of Heterogeneous Anion Exchange Membranes

A comprehensive characterization of heterogeneous anion exchange MA-40 and MA-41 membranes, differing in the nature of functional groups and the exchange capacity (3.32 and 1.41 mmol/gdry, respectively), was carried out. The MA-40 membrane contains low basic secondary and tertiary amino groups, while the MA-41 membrane contains predominantly quaternary ammonium bases. Concentration dependences of conductivity and diffusion permeability, current-voltage curves were obtained, and the transport and structural parameters of a microheterogeneous model of membrane in solutions of different natures (salts and acids) containing singly and doubly charged cations and anions (sodium and calcium chlorides, sodium sulfate and sulfuric acid). The influence of counter- and co-ions on the electrical transport properties of the studied membranes was revealed and it was shown that changes in their properties are determined not only by the nature of the electrolyte, but also by the value of the exchange capacity of the samples, as well as the nature of their functional groups.

Hyperelastic and Stacked Ensemble-Driven Predictive Modeling of PEMFC Gaskets Under Thermal and Chemical Aging.

This study comprehensively investigates the stress distribution and aging effects in Ethylene Propylene Diene Monomer (EPDM) and Liquid Silicone Rubber (LSR) gasket materials through a novel integration of hyperelastic modeling and advanced machine learning techniques. By employing the Mooney-Rivlin, Ogden, and Yeoh hyperelastic models, we evaluated the mechanical behavior of EPDM and LSR under conditions of no aging, heat aging, and combined heat- and sulfuric-acid exposure. Each model revealed distinct sensitivities to stress distribution and material deformation, with peak von Mises stress values indicating that LSR experiences higher internal stress than EPDM across all conditions. For instance, without aging, LSR shows a von Mises stress of 24.17 MPa compared to 14.96 MPa for EPDM, while under heat and sulfuric acid exposure, LSR still exhibits higher stress values, showcasing its resilience under extreme conditions. Additionally, the ensemble learning approach achieved a classification accuracy of 98% for LSR and 84% for EPDM in predicting aging effects, underscoring the robustness of our predictive framework. These findings offer practical implications for selecting suitable gasket materials and developing predictive maintenance strategies in industrial applications, such as fuel cells, where material integrity under stress and aging is paramount.

Low-Acid Leaching for Preferential Lithium Extraction and Preparation of Lithium Carbonate from Rare Earth Molten Salt Electrolytic Slag

In this work, lithium was preferentially recovered through the low-acid leaching from rare earth molten salt electrolytic slag (REMSES) with a leaching temperature of 60 °C. The influence on lithium extraction was investigated in detail in different leaching conditions. The optimal conditions were as follows: liquid-to-solid ratio (10 mL/g), sulfuric acid concentration (0.8 mol/L), leaching time (60 min) and leaching temperature (60 °C). This yielded a lithium extraction rate of 98.52% and a lithium carbonate purity of 99.5%. It was fitted using an empirical model; the kinetics showed that internal diffusion control conformed to the low-acid leaching reaction, which had an apparent activation energy of 10.81 kJ/mol for lithium. The total profit from the whole process was USD 0.2576 when dealing with 1.0 kg of REMSES. Moreover, in the sulfuric acid system, the leaching reaction mechanism was carefully investigated between 30 and 90 °C. An innovative process of recovering lithium from REMSES was achieved with environmental friendliness and good economic returns. Compared to traditional leaching using concentrated sulfuric acid, this cleaner recycling method conforms to the concept of green, low-carbon sustainable development, with high lithium selectivity, low impurity content in the filtrate and low acid consumption.

New trends in mycosynthesis of cellulose nanocrystals promoted by gamma irradiation of sugarcane bagasse

AbstractThe biological synthesis of cellulose nanocrystals (CNCs) involves utilizing cellulose-degrading microorganisms or their hydrolytic enzymes as catalysts for the controlled degradation of cellulose, yielding CNCs. Chemical synthesis of CNCs involves acid hydrolysis conducted for 45 min at 45 °C using sulfuric acid (64%). Neurospora intermedia (Assiut University Mycological Center (AUMC) 14,359), Fusarium verticillioides (AUMC 14360), and Rhizopus oryzae (AUMC 14361) were employed in the preparation of CNCs. Before both chemical and biological treatments, sugarcane bagasse (SCB) was irradiated with doses of 100, 200, and 300 kGy, enhancing the yield of nanocellulose from the cellulosic feedstock. The resultant nanocellulose was initially assessed using UV–Vis spectroscopy, and the characterization was further refined through Dynamic Light Scattering analysis to delineate particle size distribution within the nanoscale and to evaluate stability. CNCs and chemically purified cellulose (CPC) displayed analogous Fourier Transform Infrared Spectroscopy but were markedly different from SCB. X-ray Diffraction patterns revealed a notably higher crystallinity of cellulose in nanocellulose, with larger crystallite dimensions compared to CPC and SCB. Transmission Electron Microscope investigations elucidated the morphology of the synthesized nanoparticles. In summary, the selection of F. verticillioides for nanocellulose production represents a promising and sustainable approach that combines effectiveness, environmental friendliness, and cost-efficiency in the synthesis of this valuable nanomaterial. Graphical abstract

Extraction of Rare Earth Elements from Phalaborwa phosphogypsum

Rare earth elements (REE) are present at concentrations of approximately 0.36 % in phosphogypsum stacks located in Phalaborwa, South Africa. The REE are present in the phosphogypsum in solid solution in the gypsum and as fluorine and aluminium rich precipitates. Recovery of the REE offers opportunities for valorization and reducing the environmental impact of the phosphogypsum waste. This paper presents the results of investigations into the leaching behaviour of rare earth elements and other impurities from phosphogypsum using aqueous sulfuric acid. The effects of acid concentration, temperature, residence time, and the influence of impurities were evaluated for their impact on the solubility of rare earth elements in a sulfate medium. It was found that a significant fraction of the REE can be leached from the phosphogypsum in a range of conditions much less severe than traditional hard rock rare earth processing conditions. The REE were leached at a sulfuric acid concentration of 110 g/l, temperature of 30°C - 40°C and a residence time of approximately 8 hours.

Analysis of the Urine Volatilome of COVID-19 Patients and the Possible Metabolic Alterations Produced by the Disease.

Alterations in metabolism caused by SARS-CoV-2 infection have been highlighted in various investigations and have been used to search for biomarkers in different biological matrices. However, the selected biomarkers vary greatly across studies. Our objective is to provide a robust selection of biomarkers, including results from different sample treatments in the analysis of volatile organic compounds (VOCs) present in urine samples from patients with COVID-19. Between September 2021 and May 2022, urine samples were collected from 35 hospitalized COVID-19 patients and 32 healthy controls. The samples were analyzed by headspace (HS) solid phase microextraction (SPME) coupled to gas chromatography-mass spectrometry (GC-MS). Analyses were conducted on untreated urine samples and on samples that underwent specific pretreatments: lyophilization and treatment with sulfuric acid. Partial Least Squares Linear Discriminant Analysis (PLS-LDA) and Subwindow Permutation Analysis (SPA) models were established to distinguish patterns between COVID-19 patients and healthy controls. The results identify compounds that are present in different proportions in urine samples from COVID-19 patients compared to those from healthy individuals. Analysis of urine samples using HS-SPME-GC-MS reveals differences between COVID-19 patients and healthy individuals. These differences are more pronounced when methods that enhance VOC formation are used. However, these pretreatments can cause reactions between sample components, creating additional products or removing compounds, so biomarker selection could be altered. Therefore, using a combination of methods may be more informative when evaluating metabolic alterations caused by viral infections and would allow for a better selection of biomarkers.

Hydrochemical assessment of groundwater utilizing statistical analysis, integrated geochemical methods, and EWQI: a case study of Laiwu region, North China.

The investigation of groundwater quality and hydrochemical assessment holds immense significance in safeguarding and ensuring the rational utilization of groundwater resources. This study utilizes groundwater sampling and testing data from the Laiwu region (LWR), encompassing both dry and wet seasons, to delve into the hydrochemical characteristics, ion sources, and overall groundwater quality. The research findings indicate that the groundwater in LWR exhibits weak alkalinity, with the dominant ions being Ca2+ followed by Mg2+, Na+, and K+, and HCO3-, SO42-, NO3-, Cl-, and F-. The average total dissolved solids (TDS) concentrations during the dry and wet seasons are recorded as 683mg/L and 679mg/L, respectively, classifying LWR's groundwater primarily as hard-fresh water. The spatial pattern of TDS concentration in LWR displays consistency throughout both the dry and wet seasons, with relatively low TDS levels observed in the northern and southeastern regions and higher concentrations in the lower reaches of the Dawen River and nearby Gangcheng. Predominantly, Ca2+, Mg2+, and HCO3- ions in groundwater originate from the dissolution of calcite and dolomite, with the hydrogeochemical process of carbonate rock weathering involving the presence of sulfuric acid. It is noteworthy that human activities significantly impact the chemical composition of groundwater in LWR. Notably, during the dry and wet seasons, the average concentration of NO3- in groundwater is 102.81 and 106.61mg/L respectively, and the analysis shows that agricultural practice is the main source. Furthermore, the calculated average values of the entropy water quality index (EWQI) during those seasons are 58.44 and 57.24, respectively. The EWQI shows good to moderate water quality in most areas, except for a few poor-quality spots in the west. It is worth mentioning that LWR's groundwater is deemed suitable for agricultural irrigation. These research findings provide valuable insights and serve as a significant reference for the rational development and sustainable utilization of groundwater resources in the LWR region.

A simple and cost-efficient route to prepare sulfonated dihalo-monomers for synthesizing sulfonated aromatic PEMs.

We present a simple and cost-efficient route for the preparation of sulfonated dihalo-monomers for the synthesis of hydrocarbon ionomers. After conventional monomer sulfonation, excess sulfuric acid is quantitatively removed by neutralization with BaCO3. This leads to the precipitation of excess H2SO4 as insoluble BaSO4, which is easily separated from the sulfonated monomers in their soluble Ba-forms by filtration. Compared to conventional methods, the proposed approach leads to higher yields, drastically reduces the number of purification steps, and can easily be expanded to the preparation of other sulfonated monomers. The specific monomers presented here are suitable for the preparation of sulfonated polyarylenes and sulfonated polyphenylenes.

Mechanical Motion and Color Change of Humidity-Responsive Cellulose Nanocrystal Films from Sunflower Pith.

Nanocellulose has prompted extensive exploration of its applications in advanced functional materials, especially humidity-responsive materials. However, the sunflower pith (SP), a unique agricultural by-product with high cellulose and pectin content, is always ignored and wasted. This work applied sulfuric acid hydrolysis and sonication to sunflower pith to obtain nanocellulose and construct film materials with humidity-responsive properties. The SP nanoparticle (SP-NP) suspension could form a transparent film with stacked layers of laminated structure. Due to the tightly layered structure and expansion confinement effect, when humidity increases, the SP-NP film responds rapidly in just 0.5 s and completes a full flipping cycle in 4 s, demonstrating its excellent humidity-responsive capability. After removing hemicellulose and lignin, the SP cellulose nanocrystals (SPC-NC) could self-assemble into a chiral nematic structure in the film, displaying various structural colors based on different sonication times. The color of the SPC-NC film dynamically adjusted with changes in ambient humidity, exhibiting both functionality and aesthetics. This research provides a new perspective on the high-value utilization of sunflower pith while establishing a practical foundation for developing novel responsive cellulose-based materials.

High Strength Anhydrite Cement Based on Lime Mud From Water Treatment Process: One Step Synthesis in Water Environment, Characterization and Technological Parameters

ABSTRACTIn the process of water treatment from surface water sources, lime mud as waste is formed. This waste contains CaO, Ca(OH)2, and CaCO3. The article proposes a comprehensive method for processing lime mud into high‐strength anhydrite cement. The method involves the interaction of lime mud with waste sulfuric acid from the production of polymer fibers using a structure‐controlled method in the (CaO·Ca(OH)2·CaCO3)—H2SO4—H2O system at a temperature of 40°C. X‐ray diffraction analysis showed the presence of CaSO4 and CaSO4·0.62H2O phases with a purity of 99.8%. The structure‐controlled method makes it possible to control the formation and growth of calcium sulfate crystals of the required shape and size, due to which it is possible to obtain anhydrite cement with desired properties. Combined grinding of synthetic anhydrite with activator additives makes it possible to obtain anhydrite cement with a strength of up to 28.5 MPa.