Calcium Sulfate Dihydrate Research Articles

Effect of alkali metal sulfates on hydration properties of alpha-calcium sulfate hemihydrate for 3D printing

Three-dimensional printing (3DP) technology is an important means of achieving decorative convenience, personalization, and functional integration for future building construction. However, the setting time and hydration process of calcium sulfate hemihydrate (HH) present chanllenges for the 3DP application. This study aims to investigate the accelerating effect of alkali metal sulfates accelerators on the hydration transformation of HH into calcium sulfate dihydrate (DH). The setting time, conductivity, Ca2+ ion concentration, size distribution, and zeta (ζ) potential of gypsum slurries with different accelerators were measured. The results demonstrated that the accelerators significantly enhanced the hydration process of αlpha-calcium sulfate hemihydrate (α-HH). On the effect of accelerators, the setting times of gypsum slurries containing 30 wt% lithium sulfate (LS), sodium sulfate (NS) and potassium sulfate (KS) were accelerated by 82.56 %, 86.06 % and 97.13 %, respectively, compared to the control sample. The crystal particle sizes of hydration products decreased, and the absolute values of ζ potential increased to 1.85 mV, 3.1 mV, and 5.3 mV, respectively. The X-ray photoelectron spectroscopy (XPS) analysis revealed a shift in the peak values of the hardened specimens towards higher electric fields. This was accompanied by improved ion dispersion within the slurry, resulting in enhanced supersaturation of calcium sulfate dihydrate and crystallization of the crystal nuclei. Thus, the suitable accelerators can effectively achieve rapid solidification and hardening of high-fluidity gypsum slurries.

Strength analysis and microstructural characterization of calcined red mud based-geopolymer concrete modified with slag and phosphogypsum

This research aims to comprehensively investigate the combined use of calcined red mud (RM), calcium sulfate dihydrate (CSD), and ground granulated blast furnace slag (GGBFS) in geopolymer concrete (GC), demonstrating how their optimized proportions improve GC's fresh, mechanical, durability, and microstructural properties. This study investigated the influence of partially replacing calcined red mud (RM) with GGBFS and Phosphogypsum or CSD in GC. The test program included tests on the fresh, mechanical, and durability properties of these blends, including slump value, compressive strength, ultrasonic pulse velocity, water absorption and porosity, rapid chloride penetration, electrical resistivity, mass loss due to freeze-thaw cycles, and resistance to sulfate attack. Material characterization of the GC blends was conducted using scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and differential thermogravimetric analysis (DTG). One-way ANOVA analysis was also used to examine the significance of variation between the results due to the replacement of calcined RM with GGBFS and CSD. The results showed that the mix R40-G45-C15, with 40% calcined red mud, 45% GGBFS, and 15% CSD, demonstrated the highest density at 2401 kg/m³, 15.93% greater than the R70-G15-C15 mix, and achieved a compressive strength 73.40% higher at 28 days. Additionally, R40-G45-C15 showed superior durability, with water absorption and porosity reductions of 87.42% and 83.86%, an 85.78% reduction in charge passed at 7 days, and a 40.94% lower mass loss from freeze-thaw cycles compared to R70-G15-C15. SEM analysis confirmed the formation of N–A–S–H and C–A–S–H gels in the blends, contributing to improved density and strength. XRD tests indicated the nominated peaks of calcite, quartz, and portlandite in the blends, with increased portlandite intensity due to higher RM content. These results indicate that partially substituting the calcined RM with CSD and GGBFS in GC could be a viable alternative option, offering potential contributions to sustainable construction with improved structural performances.

A Newly Bio-Based Material for the Construction Industry Using Gypsum Binder and Rice Straw Waste (Oryza sativa)

Construction is one of the economic sectors with the greatest influence on climate change. In addition to working procedures, the primary carbon footprint is attributed to the choice of materials and the energy required for their manufacturing. The underlying idea of this study is to minimize the effects and offer new solutions to emerging problems in the quest for materials that can be deemed as natural, such as gypsum (calcium sulphate dihydrate) and rice straw (Oryza sativa). The acquisition of these materials involves a lower carbon footprint compared to the conventional materials. It is well known since ancient times that gypsum and cereal straw can be used in construction, with numerous examples still available. Cereal straw is one of the oldest construction materials, traditionally combined with earth and occasionally with certain binders, with it continuing to be employed in construction in many countries to this day. This work showcases the feasibility of producing stable prefabricated elements from straw waste with construction gypsum, addressing a significant environmental concern posed by the alternative of having to burn such materials. In this study, for the proposed bio-based material, specific tests, such as thermal conductivity, flexural and compressive strength, and fire resistance, were carried out to evaluate the principal physical and mechanical characteristics for different compositions of water, gypsum, and straw fiber samples. The results highlighted the good performance of the proposed materials in order to spread their use in the green building industry. The addition of straw fibers improved, in different ways, some important physical characteristics of these components so as to diminish environmental pollution and to obtain better material performance. The tests highlighted the different behaviors of the proposed material with respect to the different cuts of the straw and as well as the water/gypsum ratio; this is not very well understood and probably depends on the micro structure of the straw fibers. The blocks with raw straw showed a significant improvement in the breaking mechanism (1775.42 N) compared to the blocks with cut straw (712.26 N) when subjected to bending tests, and their performance in compression tests was also acceptable. Additionally, a very interesting reduction in thermal conductivity was achieved by incorporating rice straw (0.233 W/mK), and high fire exposure times were obtained, with gypsum preventing the spread of ignition in any type of fiber.

Gypsum Crystals Formed by the Anhydrite–Gypsum Transformation at Low Temperatures: Implications for the Formation of the Geode of Pulpí

Determining the mechanisms of the formation of giant crystals is a challenging subject. Gypsum, calcium sulfate dihydrate (CaSO4·2H2O), is known to form crystals larger than one meter in several locations worldwide. These selenite crystals grow at different temperatures, either in sedimentary or hydrothermal systems. The famous selenite crystals of the geode of Pulpí (Almería, Spain) are known to have grown at a temperature T = 20 ± 5 °C and have been proposed to form in a subaqueous environment by a self-feeding mechanism triggered by anhydrite dissolution and the ripening of microcrystalline gypsum, enhanced by oscillations in temperature. This paper reports the monitored crystallization of gypsum crystals, from anhydrite powder dissolution, inside airtight evaporation-free reactors under oscillating low temperatures (15 °C < T < 25 °C). These crystals are clearly smaller than the ones in the Pulpí mine but exhibit similar habits (i.e., single blocky crystals and twins following the 100 twinning law). The growth rate of gypsum single crystals has been measured to be between 3.8 and 35.3 µm/day. Noteworthy, we document the occurrence of the 100 contact twinning law of gypsum, which is the most widespread twinning law in natural environments but never univocally reported in laboratory experiments. The selection of the 100 contact twinning law has been correlated to the low supersaturation values obtained in the experiment, where the concentration in these long-duration experiments can be safely assumed to be the equilibrium concentration, i.e., 0.3 (at 25 °C) ≤ SI ≤ 0.4 (at 15 °C). We discuss the relevance of our experiment for forming the gypsum crystals of Pulpí in the framework of the geological history of Pulpí mineralization. These laboratory model experiments contribute to a deeper understanding of mineral nucleation and growth processes in natural environments.

Gypsum Binder With Increased Water Resistance Derived From Membrane Water Desalination Waste

ABSTRACTA method has been developed for separating a mixture of calcium, magnesium and sodium sulfates obtained through the interaction of sulfuric acid and waste from the water purification process generated by using membrane filters. The primary goal of this method is to extract gypsum and produce gypsum‐based binders. Patterns were identified regarding how various types, ratio and quantities of additives: blast furnace slag, granite screenings, portland cement, electric steel smelting slag affect the water‐gypsum ratio, strength properties, and water resistance of high‐strength gypsum binders. It was found that adding a single‐component additive specifically to enhance water resistance does not significantly impact these properties. Complex additives have been developed based on Portland cement, granulated blast furnace slag, electric furnace slag, expanded clay dust, and granite screenings of various fractions. These additives are designed to maximize the water resistance of high‐strength gypsum binder based on synthetic calcium sulfate dihydrate. As a result, the water resistance coefficient increased from 0.45 to 0.52. Additionally, a technological block diagram of the process has been proposed.

MicroED: Unveiling the Structural Chemistry of Plant Biomineralisation.

Plants are able to produce various types of crystals through metabolic processes, serving functions ranging from herbivore deterrence to photosynthetic efficiency. However, the structural analysis of these crystals has remained challenging due to their small and often imperfect nature, which renders traditional X-ray diffraction techniques unsuitable. This study explores the use of Microcrystal Electron Diffraction (microED) as a novel method for the structural analysis of plant-derived microcrystals, focusing on Armeria maritima (Milld.), a halophytic plant known for its biomineralisation capabilities. In this study, A. maritima plants were cultivated under controlled laboratory conditions with exposure to cadmium and thallium to induce the formation of crystalline deposits on their leaf surfaces. These deposits were analysed using microED, revealing the presence of sodium chloride (halite), sodium sulphate (thénardite), and calcium sulphate dihydrate (gypsum). Our findings highlight the potential of microED as a versatile tool in plant science, capable of providing detailed structural insights into biomineralisation processes, even from minimal and imperfect crystalline samples. The application of microED in this context not only advances the present understanding of A. maritima's adaptation to saline environments but also opens new avenues for exploring the structural chemistry of biomineralisation in other plant species. Our study advocates for the broader adoption of microED in botanical research, especially when dealing with challenging crystallographic problems.

Evaluation of Germination and Early Seedling Growth of Different Grasses Irrigated with Treated Mine Water

Coal mining is known to have negative impacts on the environment, necessitating land rehabilitation after mining activities. Amongst the problems associated with coal mining is the accumulation of acid mine drainage characterized by large amounts of heavy metals and high acidity. The impact of these environmental problems on the ecosystem around mining areas underscores a need to devise strategies that will ensure sustainable restoration of the ecosystem integrity to ensure environmental protection. Of these, treatment of acid mine drainage using calcium sulfate dihydrate, which is subsequently used for irrigation during phytoremediation, holds great promise for restoration of open-cast mines. However, although grasses are used for rehabilitation of coal mined areas, the impacts of treated mine water on the germination, seedling emergence, and plant growth of grasses are not well known. The aim of the study was to evaluate the germination and early seedling growth responses of different forage grasses to treated mine water. Seven forage grass species were selected, with four species represented by two varieties while others were represented by one variety, totaling 11 forage grasses. For each plant entry, 100 seeds were placed in J.R. Petri’s dishes lined with Whatman No. 2 filter paper and watered with distilled and mine water to assess germination. For the seedling establishment experiment, only five species were studied, in which twenty seeds per species were sown in pots containing mine soil and irrigated using distilled and treated mine water. The final germination percentage (FGP), germination rate index (GRI), corrected germination rate index (CGRI), and T50 were determined for the germination trail and total biomass was assessed for the seedling growth trail. The highest FGP for all grasses was attained under controlled conditions, using distilled water, ranging from 38–94%. All grasses germinated when watered using treated mine water and had a FGP ranging from 20–91%. Relative to distilled water, GRI and CGRI were highest only for L. multiflorum cv AgriBoost when seeds were watered using the treated mine water. All grasses watered with treated mine water produced high biomass for the first two weeks, after which biomass production started to decline. Two grasses, Eragrostis curvula cv Ermelo and Lolium multiflorum cv Archie, showed tolerance to treated mine water irrespective of its high electrical conductivity (557 mS∙m−1). Therefore, these grasses could be used in the rehabilitation of coal-mined areas irrigated with treated mine water.

Highly efficient CO2 mineralization: Mechanisms and feasibility of utilizing electrolytic manganese residue as a feedstock and implementing ammonia recycling

Electrolytic manganese residue (EMR) and CO2 emissions from the electrolytic manganese metal (EMM) production process present significant challenges to achieving cleaner production within the industry. Given the high capacity for CO2 sequestration and the stability of the sequestered forms, CO2 mineralization methods utilizing minerals or industrial residues have garnered considerable research interest. The efficacy of such methods is fundamentally dependent on the properties of the materials employed. EMR, due to its calcium sulfate dihydrate (CaSO4·2H2O) content, possesses an intrinsic potential for CO2 solidification. In this study, we propose a novel method for CO2 mineralization utilizing EMR, coupled with NH3·H2O recycling. Experimental results indicated that under conditions of a reaction temperature of 55 °C and a pH of approximately 8, each ton of EMR can sequester 0.16 t of CO2, with equilibrium achieved within 10 min. The mineralization mechanism was elucidated using SEM, TG curves, and XRD analyses, which revealed that Ca2+ ions are initially leached from CaSO4·2H2O in the EMR, subsequently precipitating with CO32− ions to form CaCO3. This CaCO3 layer effectively covers the surface of CaSO4·2H2O, inhibiting further Ca2+ release and stabilizing the reaction equilibrium. Furthermore, the ammonia in the solution is regenerated into NH3·H2O, facilitating its reuse and preventing secondary pollution. The utilization of EMR for CO2 mineralization not only mitigates carbon emissions in the EMM production process but also promotes environmentally sustainable practices in the industry. This study highlights a promising pathway towards achieving carbon neutrality and cleaner production in electrolytic manganese production.

Разработка способа оценки артефакта мерцания для диагностики мочевых камней на различных УЗ-сканерах.

Introduction. Today, ultrasound examination (ultrasound), due to a number of advantages over other diagnostic methods (low cost, lack of ionizing radiation, the ability to perform without restrictions on age, gender, body weight, the presence of metal objects, etc.), is widely implemented in clinical practice. However, the accuracy in detecting urinary stones in the gray-scale mode varies from 33 to 95% and depends on the experience of the specialist performing the study and the quality of the ultrasound apparatus. One of the ways to increase the diagnostic accuracy of the method is to detect the twinkling artifact (ТA). However, data on its diagnostic accuracy in detecting urinary tract stones also vary (from 50% to 97%). The reason for this is the methodological features of the conducted scientific research, as well as the technical features of the ultrasound devices used in them, in some of which (devices 2000-2010) the ТA is programmatically turned off to improve vascular visualization. In some devices developed in the last decade, the possibility of obtaining AM has been returned. However, there are no methods for detecting ТA, optimal settings of the Doppler mapping mode for better visualization. In this regard, experimental work was carried out to develop a methodology for testing the ultrasound device in order to determine the possibility of using AM. Materials and methods. In 2023, the staff of the Lopatkin Research Institute of Urology and Interventional Radiology – a branch of the Federal State Budgetary Institution «NMIC of Radiology» of the Ministry of Health of the Russian Federation and the Bauman Institute conducted a series of experiments and developed a device (phantom) that allows AM to be studied in laboratory conditions. Ultrasonic devices were used to test the device during the development process: Philips Affinity 70 and ALOKA Ultrosound F75. To test the working properties of the device, an assessment was made of the possibility of obtaining AM on a number of ultrasonic scanners: BK Specto 5000, Simens, Samsung RS65, Samsung Rs 85, Mindrey Kesona, Hitachi Arienta 750. Fragments of urinary stones of various chemical compositions were used as the studied material. Results. A device has been developed, which is a plastic container 4*10*5 see, with a side wall thickness of 0.2 cm. A substrate made of platinum- based silicone is placed inside the device, the size of 10*5*2 cm. Along the central line of the substrate, at a distance of 2 cm from each other, there are 3 recesses for fixing the concretion, with a diameter of < 5 mm. To prevent the migration of the ultrasonic sensor during the study, a fixation system is provided in the form of 2 clamps located in the upper part of the container, connected to each other by means of a toothed connection. ТА was able to register in the area of all stones, including those artificially prepared from calcium sulfate dihydrate. The optimal settings of the color Doppler mapping mode have been determined for visualization. ТА was determined in all contact media, but the most accurate, corresponding to the contours of the concretion, was obtained using ultrasonic gel. Conclusion. The conducted experimental work on ТА visualization in laboratory conditions has shown that it is possible to obtain AM in vitro using the device developed by us. The developed device greatly simplifies the configuration of the Doppler mapping mode of the ultrasound device for better visualization of ТА and makes it easy to assess the possibility of using ТА on a specific ultrasound scanner.

The Investigation of Phase Transformation Process of Nano-Citrogypsum via Recycling Saline Solution

Because citric acid may be used to preserve food, the citric acid business has grown to play a significant role in the food and beverage sector. Environmental problems with gypsum waste, or citrogypsym, resulted from the manufacture of citric acid. Calcium sulfate dihydrate (DH), with low material physical characteristics, is the primary component of gypsum. As a result, the goal of this research is to examine the phase transformation process of citrogypsum using the hydrothermal process, which is a method of recrystallizing an example solution in an appropriate setting. To do this, a recycling calcium chloride solution was used, and it was heated to 95°C for five hours under atmospheric pressure to form alpha calcium sulfate hemihydrate (α-HH). The present of -OH at 1600 cm-1 wave numbers in the FT-IR spectra of α-HH, indicates that CaSO4 has 0.5 water molecules in its crystal. Moreover, the DSC thermograms of α-HH reveal endothermic peaks at 151.2°C and 183.14°C, respectively, which correspond to the loss of 0.5 water molecules in CaSO4. The TGA thermogram of α-HH also shows a crystal water content of 4.5 wt%. Furthermore, SEM images validate the hexagonal structure of α-HH morphology. In addition, because chloride ions have an impact on corrosive materials, the saline solution can be recycled at least four times to save money and the environment.

Nitrogen Requirement and Nitrogen Form Preference by Radermachera hainanensis and R. sinica Plug Seedlings

Abstract Radermachera hainanensis Merr. and R. sinica Hemsl. are popular foliage plants raised from seeds. Nitrogen fertilizer can significantly influence medium pH and EC, plug seedling growth, and photosynthesis. Plug seedlings of both species, each with one pair of leaves, were subjected weekly to nutrient solutions with nitrogen (N) concentrations ranging from 0 to 32 mM. Nitrogen-deficient plants exhibited the lowest leaf area, SPAD-502 value, and shoot dry weight but the highest root-to-shoot ratio. Leaf area, SPAD-502 value, and root and shoot dry weights increased with increasing N concentration up to 12-16 mM, and gradually decreased thereafter. Well-grown plants with 12-16 mM N exhibited peak maximal fluorescence (Fm), photochemical quenching (qP) and the lowest minimal fluorescence (Fo) and non-photochemical quenching (qN). Seedlings received nutrient solutions with varying proportions of NH4-N: NO3-N (0:100, 25:75, 50:50, 75:25, and 100:0, in percentages) at 16 mM N. Both species exhibited reduced leaf area, SPAD-502 value, and plant dry weights when supplied with only NO3-N or NH4-N. Maximum growth was achieved at a 50% NH4-N: 50% NO3-N ratio. Species used in this study: Golden jasmine tree, Radermachera hainanensis Merr.; China Doll, Radermachera sinica Hemsl. Chemicals used in this study: ammonium nitrate; sodium dihydrogen phosphate; potassium sulphate; potassium nitrate; magnesium sulfate heptahydrate; calcium sulfate dihydrate; calcium nitrate tetrahydrate; ammonium sulfate; boric acid anhydrous; potassium chloride; ferrous sulfate heptahydrate; disodium ethylenediaminetetraacetic acid dihydrate; copper sulfate pentahydrate; zinc sulfate heptahydrate; molybdic acid; manganese sulfate monohydrate; nickel sulfate hexahydrate; sodium hydroxide.

Fabrication and histological evaluation of a self-setting granular cement using calcium sulfate hemihydrate granules with different pore distribution.

Granular type of bone substitutes is currently used in the field of dentistry to restore alveolar bone defects. However, the migration of the granules from the implantation site is still an unresolved issue. In this study, the feasibility to fabricate self-setting calcium sulfate hemihydrate (CSH) granules using different ranges of loading pressure: CSH(0), CSH(50), CSH(100), and CSH(150) was investigated with the hypothesis that CSH granules with reduced microporosity can inhibit the rapid dissolution rate of the calcium sulfate dihydrate (CSD) set blocks and induce bone regeneration. After 4 weeks of implantation, the granules were mostly replaced with new bone although no significant differences were observed. Nevertheless, the granules demonstrated the ability to set within the bone defect. It is therefore concluded that the setting ability of calcium sulfate can contribute to address the issue of migration of the granules and provide a useful guide for designing setting bone substitutes.

Investigating the Dewatering Efficiency of Sewage Sludge with Optimized Ratios of Electrolytic Manganese Residue Components.

As an industrial waste residue, Electrolytic Manganese Residue (EMR) can greatly promote sludge dewatering and further particle-size optimization can significantly strengthen sludge dewaterability. In this study, the effects of ammonium sulfate, calcium sulphate dihydrate, and manganese carbonate in EMR on sludge dewatering performance were investigated using the response surface optimization method. It was found that the optimized ratio of three components in EMR was 1.0:1.6:2.2 based on capillary suction time (CST), specific resistance of filtration (SRF), and zeta potential of dewatered sludge. The composition ratio of particle-size optimized EMR was modified based on the above optimization, resulting in a significant increase in sludge dewatering performance (CST and SRF reduced by 8.7% and 11.2%, respectively). Compared with those in original sludge, the content of bound extracellular polymeric substances in the conditioned sludge with optimized ratio was drastically reduced while that of soluble extracellular polymeric substances was slightly increased, which was in accordance with the decline of fluorescence intensity. These findings indicated the disintegration of extracellular polymeric substances, the enhancement of hydrophobicity, and dewatering properties of the sludge. In summary, optimized EMR can effectively intensify the dewaterability of sludge, providing a competitive solution for dewatering and further disposal of sludge.

Effect of Copper Chloride on Phase Structure and Properties of Synthesized Materials from Flue Gas Desulfurization Gypsum

This research investigates the influence of crystal modifying agent, copper chloride (CuCl2) (0.3, 0.45, and 0.6 g), on the phase structure and characteristics of materials derived from flue gas desulfurization (FGD) gypsum. The raw material underwent hydrothermal transformation with 0.01 M H2SO4 at 90°C for 1 hour. XRD analysis revealed a notable shift in phase structure from hexagonal calcium sulfate dihydrate (DH) in FGD gypsum to monoclinic calcium sulfate hemihydrate (alpha-HH) up to 91%in the synthesized products, with an increasing CuCl2 content. SEM analysis revealed the elongated whisker-shaped particles (110.70 µm to 207.90 µm) of alpha-HH with higher CuCl2 concentrations. Specifically, when incorporating 0.6 g of CuCl2 in 0.01 M H2SO4 at 90°C, the longest alpha-HH crystals resulted in the cast plaster with the highest flexural strength of approximately 4.92 MPa, demonstrating suitability for applications requiring sufficient mechanical strength. Thermal analysis confirmed the complete conversion of the solid phase to alpha-HH at 1200°C. Additionally, the study revealed that higher CuCl2 content led to shorter setting time. These results suggest potential applications of the present synthesized materials from FGD gypsum in industries such as ceramics casting and dental materials, where precise control over material properties is critical.

Chiral gypsum with high‐performance mechanical properties induced by self‐assembly of chiral amino acid on an amorphous mineral

AbstractFunctional chiral suprastructures are common in biology, including in biomineralization, and they are frequently found in many hardened structures of both marine and terrestrial invertebrates, and even in pathologic human otoconia of the inner ear. However, the biological processes by which they form remain unclear. Here, we show that chiral hierarchical suprastructures of calcium sulfate dihydrate (gypsum) can be induced by the chiral Aspartic acid (Asp). Left‐handed (clockwise) morphology of gypsum is induced by the d‐enantiomer of Asp, while right‐handed (counterclockwise) morphology is induced by the l‐enantiomer. A layer‐by‐layer, oriented inclination mineral growth model controlled by continuous self‐assembly of chiral Asp enantiomers on an amorphous calcium sulfate mineral surface of gypsum platelet layers is postulated to produce these chiral architectures. This hybrid amorphous‐crystallized chiral and hierarchical suprastructure of gypsum displays outstanding mechanical properties, including high‐performance strength and toughness. Furthermore, the induction of chiral gypsum suprastructures can be more generally extended from specific acidic amino acids to other (nonamino acid) molecules. These findings contribute to our understanding of the molecular mechanisms by which biomineral‐associated enantiomers exert structural control over chiral architectures commonly seen in biominerals and in biomimetically synthesized functional materials.

Durable lightweight cementitious composites incorporating rice husk: Accelerated aging studies with acidic and basic solutions

This study investigates the compatibility between cellular concrete (foamed concrete) and natural rice husk to develop high-performance and sustainable sealing materials. Through a bibliographical review we identified challenges in incorporating vegetable fibers into cementitious matrices due to problems related to durability. Prismatic samples of a Reference mixture (foamed concrete) and a Composite with foamed concrete and natural rice husk underwent chemical treatments with acidic and basic solutions to simulate long-term durability. Results show that even after complete organic matter degradation, the composite maintains adequate mechanical performance for sealing walls. Microstructural analyses, including scanning electron microscopy, x-ray diffraction, x-ray fluorescence, and energy dispersive spectroscopy, revealed that silica in the rice husk significantly contributes to axial compression strength by forming C–S–H. The degradation of natural polymers results in the formation of calcium carbonate and calcium sulfate dihydrate, mitigating strength loss. This study proves that the composites with natural rice husk and foamed concrete are a viable and durable solution, provided it does not include metallic materials susceptible to corrosion in composition.

Sustainable Production and Physicochemical Characteristics of Calcium Sulfate Dihydrate Prepared from Waste Eggshells

Sustainable Production and Physicochemical Characteristics of Calcium Sulfate Dihydrate Prepared from Waste Eggshells

Change in Microstructure, Mechanical Strength, Fire Resistance, and Radiation Attenuation Properties of Gypsum Plaster with Boric Acid

AbstractIn this study, the effect of boric acid addition on the microstructure of gypsum plaster was investigated to determine an environmentally friendly gypsum additive that may enhance mechanical strength, fire resistance, and X-ray radiation attenuation properties. The mechanical strengths of bare gypsum and boric acid-added (0–0.5% by weight with respect to gypsum amount) gypsum plasters were evaluated in terms of compressive and bending strengths. The effects of the different addition procedures of boric acid (0.1% by wt.) on the fire resistance of the gypsum plasterboard were also evaluated. X-ray radiation attenuation properties of boric acid-added (0.1% by wt.) gypsum plasterboard were investigated as well. XRD, ATR-FTIR, Helium pycnometer, N2 adsorption–desorption, and SEM analysis were performed to determine the microstructural properties of gypsum plaster. XRD and ATR-FTIR analysis revealed that boric acid did not change the calcium sulfate dihydrate structure of gypsum plaster. Whereas, Helium pycnometer, N2 adsorption–desorption, and SEM analysis showed that the physical properties of gypsum changed with an increase in pore volume, skeletal density, and particle size after boric acid addition. The increase in the pore volume and particle size decreased the mechanical strength of gypsum. However, boric acid addition on the gypsum plaster plate, especially using the spraying method, enhanced the fire resistance of gypsum. Additionally, boric acid slightly enhanced the X-ray radiation attenuation properties (0.7%) of the gypsum plasterboard.

Sustainable Production of Chitin Nanowhiskers from Crustacean Biomass Using Cost-Effective Ionic Liquids: Strategies to Avoid Byproduct Formation

Nanochitin, especially in the form of chitin nanowhiskers (ChNWs), represents a significant advance in biopolymer technology due to its high specific surface area, superior tensile strength, and excellent thermal stability. Derived from crustacean waste, which contains 15–40% of chitin, these materials provide a sustainable option that diverts waste from landfills and contributes to environmental conservation. Traditional methods of isolating nanochitin are energy-intensive and generate substantial waste. This study introduces a more sustainable method using inexpensive ionic liquids (ILs) such as [Hmim][HSO4] and [HN222][HSO4], which bypass the costly and destructive steps of traditional procedures. This study also identified the byproduct in IL-mediated chitin hydrolysis reaction as calcium sulfate dihydrate and presented a solution to circumvent the byproduct formation. The effectiveness of the [HN222][HSO4] IL in producing ChNWs from both purified chitin and crustacean biomass was assessed, showing a high yield and maintaining the purity and structural integrity of chitin, thereby demonstrating a significant reduction in the environmental footprint of ChNW production.

Chemical and radiochemical characterization of phosphogypsum from Poland

Abstract The current study presents the results of the chemical and the radiochemical characterization of phosphogypsum obtained from the former Wizów Chemical Plant in Poland. Phosphogypsum is a residue obtained from phosphoric acid production. Phosphogypsum mainly contains calcium sulfate dihydrate and impurities originating from the source phosphate rock, including toxic trace elements and natural radionuclides. The phosphogypsum stacks occupy a large area and are an environmental issue today. The project “Phosphogypsum Processing to Critical Raw Materials”, currently realized at the Institute of Nuclear Chemistry and Technology, focuses on the use of phosphogypsum from the Polish stacks as material to recover rare earth elements (REEs). The remaining gypsum matrix can be used as an inexpensive material in construction. The chemical and radiological characterization of the radioactive isotopes present in phosphogypsum was performed by using inductively coupled plasma mass spectrometry (ICP-MS) and the gamma spectrometry technique. The radioactivity of the Polish phosphogypsum was then compared with the radioactivity of the phosphogypsum waste present worldwide.