Formation Of CaCO3 Research Articles

Synergistic mechanisms of magnesium slag coupled with dust removal ash for CO2 sequestration via direct aqueous carbonation: High mineralization efficiency and optimization of reaction parameters

Utilizing natural industrial solid waste for CO2 capture and utilization can reduce both the environmental problems caused by industrial solid waste and greenhouse gases. Based on this idea, magnesium slag-based solid waste has great economic and environmental value as CO2 storage and backfill material. In this study, the CO2 mineralization capacity and efficiency of two magnesium slag-based industrial solid wastes including magnesium slag (MS) and dust removal ash (DRA) and their mixtures were studied by gas-liquid two-phase mineralization method. The as-prepared samples were characterized by a series of techniques such as XRF, XRD, SEM, FT-IR and TG tests. The results exhibited that compared with single MS and DRA sample, the mineralization efficiency of composites increased 7.63 % and 14.1 %, respectively, which performed a synergistic effect. In addition, the main operation parameters including reaction temperature, solid-to-liquid ratio and CO2 concentration were investigated, and the temperature of 35 ℃, solid-to-liquid ratio of 0.1 g/mL and CO2 concentration of 30 vol% were chosen as optimum operating parameters. Furthermore, the reaction mechanism of CaCO3 formation and the mineralization efficiency improvement after cooperation were expounded.

Enhanced inhibition of heavy metal leaching in incineration bottom ash through accelerated carbonation with ammonium carbonate

The increasing generation of incineration bottom residues poses environmental risks due to heavy metal leaching, while carbonation is one of the effective methods to immobilize heavy metals. This study introduces a novel approach to mitigate heavy metal leaching from incineration bottom ash (IBA) by accelerated carbonation with ammonium carbonate solution. The effect of ammonium carbonate concentration on carbonation efficiency and inhibition of heavy metal leaching was systematically investigated. X-ray fluorescence was used to analyze the composition of IBA, and thermogravimetric analysis (TGA) and inductively coupled plasma optical emission spectroscopy/mass spectrometry were used to determine carbonation capacity and heavy metal leaching, respectively. Results showed that maximum carbonation capacity was achieved at 8 wt% ammonium carbonate concentration at a solid/liquid ratio of 1:5 for 1 h, but the increase in carbonation efficiency slowed down when the concentration exceeded 4 wt%. Ammonium carbonate accelerated carbonation effectively inhibited heavy metal leaching, particularly copper, with an 89% inhibition rate at 10 wt% ammonium carbonate, while diminished effects were observed with chromiun. The effect of the ammonium carbonate concentration on heavy metal inhibition became less significant above 4 wt%, revealing a nuanced relationship between carbonation and heavy metal leaching inhibition. TGA and X-ray diffraction analyses confirmed the formation of insoluble CaCO3 during carbonation, elucidating neomineralization processes that immobilize trace heavy metals. In addition, the study explored the impact of carbonation on leachate pH, emphasizing the interplay between pH reduction and heavy metal leaching inhibition.

A fully coupled solid-particle microphysics scheme for stratospheric aerosol injections within the aerosol–chemistry–climate model SOCOL-AERv2

Abstract. Recent studies have suggested that injection of solid particles such as alumina and calcite particles for stratospheric aerosol injection (SAI) instead of sulfur-based injections could reduce some of the adverse side effects of SAI such as ozone depletion and stratospheric heating. Here, we present a version of the global aerosol–chemistry–climate model SOCOL-AERv2 and the Earth system model (ESM) SOCOLv4 which incorporate a solid-particle microphysics scheme for assessment of SAI of solid particles. Microphysical interactions of the solid particle with the stratospheric sulfur cycle were interactively coupled to the heterogeneous chemistry scheme and the radiative transfer code (RTC) for the first time within an ESM. Therefore, the model allows simulation of heterogeneous chemistry at the particle surface as well as feedbacks between microphysics, chemistry, radiation and climate. We show that sulfur-based SAI results in a doubling of the stratospheric aerosol burden compared to the same mass injection rate of calcite and alumina particles with a radius of 240 nm. Most of the sulfuric acid aerosol mass resulting from SO2 injection does not need to be lifted to the stratosphere but is formed after in situ oxidation and subsequent water uptake in the stratosphere. Therefore, to achieve the same radiative forcing, larger injection rates are needed for calcite and alumina particle injection than for sulfur-based SAI. The stratospheric sulfur cycle would be significantly perturbed, with a reduction in stratospheric sulfuric acid burden by 53 %, when injecting 5 Mt yr−1 (megatons per year) of alumina or calcite particles of 240 nm radius. We show that alumina particles will acquire a sulfuric acid coating equivalent to about 10 nm thickness if the sulfuric acid is equally distributed over the whole available particle surface area in the lower stratosphere. However, due to the steep contact angle of sulfuric acid on alumina particles, the sulfuric acid coating would likely not cover the entire alumina surface, which would result in available surface for heterogeneous reactions other than the ones on sulfuric acid. When applying realistic uptake coefficients of 1.0, 10−5 and 10−4 for H2SO4, HCl and HNO3, respectively, the same scenario with injections of calcite particles results in 94 % of the particle mass remaining in the form of CaCO3. This likely keeps the optical properties of the calcite particles intact but could significantly alter the heterogeneous reactions occurring on the particle surfaces. The major process uncertainties of solid-particle SAI are (1) the solid-particle microphysics in the injection plume and degree of agglomeration of solid particles on the sub-ESM grid scale, (2) the scattering properties of the resulting agglomerates, (3) heterogeneous chemistry on the particle surface, and (4) aerosol–cloud interactions. These uncertainties can only be addressed with extensive, coordinated experimental and modelling research efforts. The model presented in this work offers a useful tool for sensitivity studies and incorporating new experimental results on SAI of solid particles.

Influence of ultra-fine pozzolanic materials on the self-healing capabilities of ultra-high performance concrete under carbonation conditioning

This work studies the autogenous self-healing of ultra-high performance concrete (UHPC) incorporating two ultra-fine pozzolanic materials, silica fume (USF) and ultra-fine fly ash (UFFA), under carbonation conditioning. Both ultra-fine pozzolanic materials stimulate the healing of cracks by promoting the secondary hydration of the cement matrix. USF and UFFA form healing products primarily consisting of C-S-H and ettringite, respectively, and the latter product closes the cracks more effectively. Under carbonation conditioning, UFFA accelerates CaCO3 formation with residual uncarbonated ettringites as the structural skeleton, improving the impermeability recovery. USF generates silica gel as a bonding layer between the CaCO3 crystals and the cement matrix after decalcification, which induces more multi-dimensional cracking upon regenerated structures under flexural reloading, thereby enhancing the mechanical property restoration of UHPC. UFFA-modified UHPC is ideal for applications requiring high impermeability, whereas USF-incorporated UHPC is better suited for scenarios with high load-bearing demands.

Impact of edetate sodium on calcium carbonate scaling: Insights from molecular dynamics simulations

In order to mitigate calcium carbonate (CaCO3) scaling in oil and gas wells, antiscaling agents are commonly used. This research employed the molecular dynamics method to simulate the crystallization process of a supersaturated CaCO3 solution, with particular emphasis on examining the influence of the antiscalant edetate sodium (EDTA). Analysis of the spatial distribution of Ca2+ in proximity to CO32− revealed that EDTA effectively impedes the interaction between Ca2+ and CO32−, resulting in a reduction in the mean square displacement and diffusion coefficient of CO32−. The examination of intermolecular interaction energies indicates that the binding energy between Ca2+ and CO32− is approximately −516 kcal mol−1, while the binding energy between Ca2+ and EDTA is estimated at −718 kcal mol−1. These findings suggest that EDTA exhibits a higher affinity for binding with Ca2+ compared to CO32−, consequently hindering the formation of CaCO3.

Optimizing the content of Li2CO3, Na2SO4 and TEA in fly ash–cement system by response surface methodology

With an optimized dosage, hardening accelerators become a vital means of modifying fly ash-cement system (FAC). This study comprehensively investigated the mechanical properties of FAC modified by Li2CO3, Na2SO4, and triethanolamine (TEA) under different dosages, and optimized the dosage of accelerators through the response surface method (RSM). The synergistic effect of accelerators on the hydration of FAC was characterized by thermogravimetric differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results demonstrated that the factors and response value followed a quadratic polynomial model. The regression coefficients R2 of the model were all greater than 0.9, indicating good agreement with the experimental data. The content of Li2CO3 and Na2SO4 had an extremely significant effect on the compressive strength of 1d and 3d, followed by TEA. The optimal mix ratio predicted by RSM was 0.12 % Li2CO3, 0.47 % Na2SO4, and 0.40 % TEA. Early hydration stages revealed that the combined action of these accelerators increased the formation of CH, CaCO3, and amorphous C-(A)-S-H gel. Microscopically, the surface of fly ash exhibited alkali-induced corrosion, thereby enhancing its pozzolanic reactivity.

Investigating reactive transport and precipitation patterns of calcium carbonate in fractured porous media

HypothesisUnderstanding calcium carbonate (CaCO3) precipitation in various polymorphs from nanoparticle size (amorphous calcium carbonate) to microparticle size (vaterite, aragonite, dendrite, calcite) is important for practical applications, including carbon geo-storage (e.g., basalt formations), hydrogen storage, groundwater management, and soil stabilization. Our hypothesis suggests that the interplay of Péclet numbers (Pe), Damköhler numbers (Da), and Supersaturation Index (SI) significantly impacts the evolution of CaCO3 precipitation in fractured porous media in terms of mixing patterns, spatiotemporal evolution, crystal morphology, crystal size, and clogging behavior. ExperimentsThis study takes a novel approach to explore the colloidal formation and precipitation dynamics of CaCO3 within a fractured microfluidic system. Here, calcium chloride (CaCl2) and sodium bicarbonate (NaHCO3) solutions were injected and reacted under varied Pe (0–11), Da (0–1), and SI (2–5). FindingsOur analysis revealed distinct precipitation patterns and mixing types, such as transverse, longitudinal, and incomplete mixing, providing insights into the behavior in fractured porous media. We systematically analyzed the temporal and spatial evolution of precipitation, demonstrating how Pe, Da, and SI dictate precipitation rates and spatial distribution. Additionally, the study uncovered a range of CaCO3 polymorphic forms, illustrating their evolution and coexistence. Morphological changes and crystal sizes were examined to decode nucleation and growth processes. Significantly, our findings highlight the relationship between precipitation and clogging in the fractured medium, offering a deeper understanding of reactive transport in complex porous environments. These insights are crucial for enhancing carbon containment security and storage efficiency in underground formations, improving groundwater remediation techniques, and developing novel construction materials through controlled precipitation processes.

Role of bacteria on bio-induced calcium carbonate formation: insights from droplet microfluidic experiments

Microbially induced calcium carbonate precipitation (MICP) has emerged as a promising solution for geotechnical issues. However, the role of bacteria in the formation of calcium carbonate (CaCO3) remains incompletely understood. In this study, a droplet microfluidic chip was developed to observe the growth process of calcium carbonate and bacterial behaviour during the MICP process under various bacterial density conditions. Scanning electron microscope was then utilised to analyse the calcium carbonate morphology, and Raman spectroscopy was employed to identify calcium carbonate polymorphs. Nucleation within microspaces showed a stochastic nature. Within the droplets where crystals formed, all crystals manifested as cubic calcite. Higher bacterial density led to the formation of larger and more irregularly shaped crystals, with crystal size showing a significant correlation with urease activity. In droplets where no crystals formed, higher bacterial density and urease activity resulted in the precipitation of amorphous calcium carbonate on the bacterial surface. However, this precipitation pattern differed from the formation of monocrystalline calcium carbonate. The results demonstrate that bacteria act primarily as urease secretors to regulate crystal growth during the MICP process, while their role as nucleation sites for crystals remains debatable. This study provides new insights into the bio-induced calcium carbonate formation mechanism.

CeO2 enhanced performance of NiFe2O4-CaO for carbon capture and in-situ hydrogenation conversion to CO

NiFe2O4 exhibits excellent redox properties and is widely applied in CaO-NiFe2O4 chemical looping processes. However, rapid sintering of Ni-Fe alloy under reaction conditions limited its industrial applications. The CeO2-NiFe-CaO were synthesized through a physical mixing method with NiFe2O4 as a precursor, and its CO2 capture capacity and in-situ hydrogenation performance were conducted on ICCC-RWGS reaction under different conditions. 20CeO2-NiFe-CaO exhibited a CO yielding of 9.35 mmol/g at 650 °C. During the carbon capture stage, CO2 was adsorbed by CaO, leading to the formation of CaCO3. In the hydrogenation conversion stage, hydroxyl groups were generated on the surface, combining with CaCO3 to produce formate species, further generating H2O and CO. 15CNF-CaO exhibited superior cyclic ICCC-RWGS reaction performance compared to 15NF-CaO, with a CO yield of 1.88 mmol/g after 40 cycles. CeO2 inhibited the sintering of catalytic components, preserving a higher specific surface area and smaller particle size. Furthermore, CeO2 in 15CNF-CaO inhibited carbon deposition and enhanced in-situ hydrogenation performance, exhibiting better CaO regeneration capability and better cyclic stability. These results could provide insight for designing the DFMs for the ICCC-RWGS process.

In Situ Monitoring the Nucleation and Growth of Nanoscale CaCO3 at the Oil-Water Interface.

Interfaces can actively control the nucleation kinetics, orientations, and polymorphs of calcium carbonate (CaCO3). Prior studies have revealed that CaCO3 formation can be affected by the interplay between chemical functional moieties on solid-liquid or air-liquid interfaces as well as CaCO3's precursors and facets. Yet little is known about the roles of a liquid-liquid interface, specifically an oil-liquid interface, in directing CaCO3 mineralization which are common in natural and engineered systems. Here, by using in situ X-ray scattering techniques to locate a meniscus formed between water and a representative oil, isooctane, we successfully monitored CaCO3 formation at the pliable isooctane-water interface and systematically investigated the pivotal roles of the interface in the formation of CaCO3 (i.e., particle size, its spatial distribution with respect to the interface, and its mineral phase). Different from bulk solution, ∼5 nm CaCO3 nanoparticles form at the isooctane-water interface. They stably exist for a long time (36 h), which can result from interface-stabilized dehydrated prenucleation clusters of CaCO3. There is a clear tendency for enhanced amounts and faster crystallization of CaCO3 at locations closer to isooctane, which is attributed to a higher pH and an easier dehydration environment created by the interface and oil. Our study provides insights into CaCO3 nucleation at an oil-water interface, which can deepen our understanding of pliable interfaces interacting with CaCO3 and benefit mineral scaling control during energy-related subsurface operation.

Use of rise husks to improve the efficiency of MICP-based soil improvement technique

Biogrouting has been identified as the best alternative approach for the conventional cement and chemical grouts. Among the various types of biogrouting techniques, microbial induced carbonate precipitation (MICP) has been recently recognized as a promising pathway for producing biogrout material, hence densifying the weak soils. In MICP, calcium carbonate (CaCO3) biocement is produced through biochemical reactions induced by the urease enzyme. The efficiency and productivity of MICP can be further improved by introducing various additives, including fibers, organic polymers, powders, waste materials, etc. In this research, rice husk was sustainably incorporated into the MICP process, and (i) the effect of the rice husk content, (ii) the concentration of the cementation solution and (iii) the treatment time on the unconfined compressive strength (UCS) of the sandy soil were investigated at the laboratory-scale. Cementation solutions with higher concentrations exhibited a higher UCS values than solutions with lower concentrations. Interestingly, the content of rice husk had a marked influence on the UCS, and the optimum rice husk content was 15%. Compared to that of the control sample (0% rice husk), a threefold greater UCS was obtained for 15% of the rice husk content sample. The outcomes further suggested that longer treatment with lower concentration of cementation solution was the best combination for achieving effective cementation within the sand matrix. Rice husk acted as the template for CaCO3 crystals to nucleate while promoting the efficient formation of CaCO3, indicating that the rice husk is an excellent additive to improve the efficiency of the MICP biocementation in a sustainable way.

Biodiesel production, calcium recovery, and adsorbent synthesis using dairy sludge

Dairy sludge (DS) consists of organic compounds such as lipids and valuable inorganic elements. Biodiesel recovery from dairy sludge extract (DSE), using conventional acid (trans)esterification yielded only 16.5 wt%. In contrast, non-catalytic (trans)esterification generated a substantially higher biodiesel yield of approximately 74.0 wt% due to the method’s tolerance for impurities. Defatted dairy sludge (DDS) contained a higher Ca concentration than DS. DDS-produced biochar (DDSB) increased its Ca concentration predominantly in the form of CaO. 91.1% of the Ca was recovered from the DDSB containing Ca. The Ca remaining in the biochar residue (DDSBR) after Ca recovery was in the form of CaCO3. The porous structure developed as the Ca dissolved, implying that DDSBR could be an effective pollutant adsorbent. In this study, a method is proposed to maximize the utilization of DS by producing biodiesel, recovering Ca content, and using it as a pollutant adsorbent.

Self-healing performance of engineered geopolymer composites subjected to sodium sulphate

Engineered geopolymer composites (EGCs) have self-healing potential due to their multiple fine-cracking features. However, water immersion, as a self-healing condition for fibre-reinforced cement-based composites, may limit the self-healing ability of EGCs due to water would not directly participate in the precipitation reaction. By contrast, sodium sulphate is proved as an effective activator to promote the geopolymerisation process, while the self-healing performance of EGCs exposed to sodium sulphate has not been comprehensively demonstrated in the literature. Therefore, this paper investigates the self-healing performance of the EGCs subjected to sodium sulphate (Na2SO4) under wet-dry cycles. The results show that the EGCs preloaded at 3 days attain a higher increment of C-(A)-S-H gels at the cracks than those preloaded at 28 days, indicating the EGCs cracked at the early age have better self-healing performance under sulphate exposure. Besides, ettringite and calcium carbonate are detected as the self-healing products in the EGCs preloaded at 3 days, while the ettringite cannot be found in the EGCs preloaded at 28 days. The EGCs exposed to 5 % Na2SO4 solution and wet-dry cycles can achieve self-healing by forming more CaCO3. Increasing the Na2SO4 concentration to 10 % can accomplish self-healing by facilitating the C-(A)-S-H and CaCO3 formation, enhancing the tensile stiffness recovery and crack width reduction ratios for the EGCs with tensile strains of 2 % and 4 % at 3 days. Decreasing the preloading level also improves the tensile stiffness recovery and crack width reduction ratios regardless of the Na2SO4 concentration and preloading age, since the self-healing products are easier to fill the small cracks. Through a combination of Na2SO4 solution and wet-dry cycles, this study develops a new strategy for the accomplishment of self-healing of EGCs.

Alkaline activation via in-situ caustification of one-part binders of composite precursors of waste glass and limestone

Mixtures of powders of waste glass (WG), limestone (LS), Na2CO3 and CaO were used to formulate novel one-part in situ alkali-activated cement (WG-AAC). The in-situ interaction Na2CO3-CaO-H2O promoted the formation of CaCO3 and NaOH, which promoted the WG and LS dissolution and influenced the micro- and molecular features of the resulting cementitious products. Pastes and mortars developed 1-year strengths of up to 29 MPa and were stable underwater. Characterization by XRD, SEM, EDS, and 29Si-NMR indicated that a Na2CO3:CaO ratio close to 1:1 resulted in polymerized C-S-H, CaCO3, silica gel, and Ca-modified silica gel, which were intimately intermixed and possibly crosslinked through Q3 bonds. Such phases interacted synergistically improving the underwater stability of the WG-AAC, indicating that in-situ caustification is a suitable and practical alkaline activation for SiO2-rich precursors.

Blue carbon storage in a sub-Antarctic marine protected area

High-latitude ecosystems have been overlooked in carbon budgets, which traditionally focus on mangroves, salt marshes, and seagrasses. The benthic assemblages and their Nature Contributions to People in Namuncurá – Burdwood Bank I and II, two offshore sub-Antarctic Marine Protected Areas (MPAs), are the conservation values. Here we show that the carbon reservoirs of these MPAs can be greater than those of their Antarctic counterparts, which, together with their extension, emphasize the need to maintain their protected status. Considering their total area, these MPAs stored in biomass 52,085.78 Mg C, corresponding 34,964.16 Mg to organic carbon (OC) and 17,121.62 Mg to inorganic carbon (IC). Surficial sediments stored 933,258,336 Mg C with 188,089,629 Mg of OC and 745,168,707 Mg of IC. However, when accounting for CO2 production through CaCO3 precipitation, the IC fractions decrease to 3,150.37 Mg C and 137,111,042 Mg C for biomass and sediments, respectively. We assume low sediment deposition due to the oceanic location, as direct sedimentation rates for these areas are unavailable. Most blue carbon assessments have focused solely on OC, despite the formation of CaCO3 releases CO2, decreasing net carbon storage. We compared various approaches for incorporating carbonates into carbon estimations. These results underscore the importance of including IC into carbon assessments and highlights the importance of sub-Antarctic benthic ecosystems as nature-based solutions to climate change.

Reaction mechanism of Ca(OH)2-based carbon storage suitable for the production of building materials

The development of CaCO3 oxyfuel combustion and calcium looping techniques offers opportunities for Ca(OH)2 production with near-zero CO2 emissions. This study investigated the viability of Ca(OH)2-based CO2 storage for use in the production of building materials. To resolve the deficient strength gain of Ca(OH)2 carbonation, siliceous materials, using fly ash as a model compound, were introduced into the raw mixture, and hydrothermal curing was applied to promote the pozzolanic reaction. Two microstructural features, i.e., inner and outer CaCO3 formations, were identified during Ca(OH)2 carbonation via backscattered electron imaging. Inner CaCO3 formation is characterized by Ca(OH)2–CaCO3 conversion within the edge of Ca(OH)2 particles. Outer CaCO3 formation is characterized by the dissolution of Ca(OH)2 and the precipitation of CaCO3 in capillary pores, which generates hollow microstructures. The hollow space can be further filled by Al-tobermorite during hydrothermal curing. The prepared materials are capable of storing up to 16 % CO2 by the mass of the raw mixture. Furthermore, the pore structure influenced by inner and outer CaCO3 formation demonstrates the feasibility of adjusting the material's mechanical and CO2 storing properties by controlling the carbonation and hydrothermal curing schemes.

Assessing the carbonation potential of wood ash for CO2 sequestration

Wood ash, a byproduct of wood combustion, poses environmental challenges when disposed of in landfills. This study explores a sustainable alternative by investigating the carbonation of wood ash, a process converting CO2 into stable carbonate minerals. With increasing concerns about waste management, this research aims to identify optimal carbonation conditions by varying relative humidity, liquid-to-solid ratio (L/S), and temperature. Results demonstrate that the ideal conditions for wood ash carbonation involve a moderate relative humidity of 55%, room temperature at 25 °C, and a lower L/S ratio. Thermogravimetric analysis (TGA) indicates that extended curing times increase CaCO3 formation. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) confirm the presence of carbonate phases. Mechanical strength tests reveal that samples with lower porosity and higher carbonation products exhibit superior strength. This study contributes to the understanding of wood ash carbonation but also emphasizes its potential practical applications in construction materials as light aggregates in cement concrete. The research explores the implications for sustainable waste management, offering insights into environmentally and economically viable solutions for wood ash recycling.

Early age accelerated carbonation of cementitious materials surface in low CO2 concentration condition

Accelerated carbonation curing contributes to the carbon sequestration effect of cementitious materials and enhances surface density. However, in large-scale applications, traditional high CO2 concentration conditions (>5 % CO2) are constrained by economic costs. This study traces the early-stage accelerated carbonation process of cement mortar under low CO2 concentration (3 % CO2) condition from the perspectives of the evolution of CaCO3 crystal types, phase transformations, and microstructural changes, and compares the results with those under the 20 % CO2 condition. The results show that the carbonation depth of mortar specimens cured under the 3 % CO2 condition is shallower, but the cumulative concentration of CaCO3 within the surface 3 mm is not significantly lower than that under the 20 % CO2 condition; The carbonation zone generates more low-crystalline forms of CaCO3; The accelerated carbonation process does not affect the formation of CH and ettringite. Microscopic results indicate that under the 3 % CO2 condition, the synergistic effects of hydration and carbonation are better, and appropriately extending the curing time helps to refine the pore structure of the carbonation zone and improve the density of the substrate surface.

Study on the Scale and Corrosion Inhibition Effect of Curcumin‐Based Novel Polymers

AbstractThe curcumin‐malic acid‐aspartic acid polymer (PCMA) as a new water treatment agent was prepared by solid phase synthesis of curcumin, malic acid and aspartic acid. The static scale inhibition experiments showed that PCMA can inhibit CaCO3 and CaSO4 scale formation by 100.0 % and had excellent scale inhibition effect under various experimental conditions. The mechanism of action of PCMA was obtained by X‐ray diffraction, scanning electron microscope and molecular dynamics simulation. Electrochemical test showed that PCMA is an anodic corrosion inhibitor that achieves 93.1 % corrosion inhibition by forming a protective film on the surface of Q235 carbon steel. Besides, fluorescence spectra proved that PCMA has stable fluorescence intensity.

Synthesis of Calcium Carbonate from Orange Peel Waste Extract: A Mechanistic Investigation

The present work reports the mechanism and synthesis of calcium carbonate (CaCO3) formation from orange peel, which is one of the most common agriculture waste generated throughout the globe. The zest of oranges was co-distilled with distilled water to separate the essential oil content. Further, the residue was washed twice with distilled water to get the desired extract. For the green synthesis of CaCO3, a saturated solution of calcium nitrate tetrahydrate (Ca(NO3)2·4H2O) was mixed thoroughly with orange peel extract in the 1:3 proportion. This solution was kept on magnetic stirrer while maintaining temperature at 85˚C, heated at 100˚C for 13 h which was further annealed at 300˚C, 500˚C and 700˚C. X-ray diffraction (XRD) shows the presence of calcite phase corresponding to CaCO3. Fourier transform infrared spectra (FTIR) exhibits the bands corresponding to Ca-O, C-O and vibrations of CO3-2 bonds whereas UV–Visible spectroscopy shows the optical behavior of CaCO3. The qualitative analysis of orange peel extract as well as the black-brown gel formed as a result of sol–gel synthesis method was examined using Gas Chromatography & Mass Spectrometry (GCMS). It revealed the presence of acidic groups (2,3-butanediol & 1,4-benzenediol) which led to the development of a mechanism, governing the formation of CaCO3.