Distribution Of Functional Groups Research Articles

Kinetics of pyrolysis and Computational Fluid Dynamics modeling of low metamorphic coal

AbstractThis study explores the low‐temperature pyrolysis kinetic of low metamorphic grade coal from Northern Shaanxi, utilizing Fourier transform infrared (FT‐IR) spectroscopy to analyze the characteristics of various functional groups over a 293–1023 K temperature range. A kinetic model, correlating with the pyrolysis behaviors of these groups, was developed through thermal analysis kinetics. Computational fluid dynamics (CFD) technology simulated the furnace's flow dynamics, allowing an examination of the physical field alterations and functional group evolution during pyrolysis. Results showed that the pyrolysis kinetic functions for aromatic C–H, C=C, C–O, and •OH, along with temperature, pressure, and velocity fields, were successfully integrated into the simulation. This integration provided detailed insights into the temperature profile, pressure distribution, flow velocities, and functional group distribution in the furnace. Aliphatics, exhibiting the largest mass fraction and wide pyrolysis temperature range, and •OH radicals with the highest activation energy were concentrated in the furnace's pyrolysis zone center. C=C's distribution was influenced by aromatic C–H and aliphatics, showing a complementary pattern. The oxygen‐containing groups C–O and C=O had similar pyrolysis mechanisms and uniform distribution. The functional groups' mass fractions were ranked from highest to lowest as follows: aliphatics > •OH > aromatic C–H > C–O > C=C > C=O.

Developing plant functional groups to identify changes in functional composition and diversity in a dryland river experiencing artificially sustained flows

Land use and climate changes are driving significant shifts in the magnitude and persistence of dryland stream surface flows. The impact of these shifts on ecological functioning is largely unknown, particularly where streams have become wetter rather than drier. This study investigated relationships between hydrologic regime (including surface water persistence, differences in groundwater depth and altered flooding dynamics) with plant traits and riverine vegetation functional composition. Our study system was a previously ephemeral creek in semi-arid northwest Australia that has received groundwater discharge from nearby mining operations for >15 years; surface flows are now persistent for ∼27 km downstream of the discharge point. We aimed to (i) identify plant functional groups (FGs) associated with the creek and adjacent floodplain; and (ii) assess their distribution across hydrological gradients to predict shifts in ecological functioning in response to changing flow regimes. Seven FGs were identified using hierarchical clustering of 40 woody perennial plant species based on morphometric, phenological and physiologic traits. We then investigated how FG abundance (projective foliar cover), functional composition, and functional and taxonomic richness varied along a 14 km gradient from persistent to ephemeral flows, varying groundwater depths, and distances from the stream channel. Dominant FGs were (i) drought avoidant mesic trees that are fluvial stress tolerant, or (ii) drought tolerant xeric tall shrubs that are fluvial stress intolerant. The drought avoidant mesic tree FG was associated with shallow groundwater but exhibited lower cover in riparian areas closer to the discharge (persistent surface flows). However, there were more FGs and higher species richness closer to the discharge point, particularly on the floodplain. Our findings demonstrate that quantifying FG distribution and diversity is a significant step in both assessing the impacts of mine water discharge on riverine ecosystems and for planning for post-mining restoration.

Electrophile-mediated ionic liquid strategy for transforming inert natural polymers into highly active iodine adsorbents

The separation and conversion of gas resources are crucial aspects of sustainable energy development. Developing general methods to overcome bottlenecks in gas adsorption and conversion within natural polymers is an urgent global concern. In this work, the use of ionic liquids as electrophiles was proposed, and the Ionic Liquid Solution Process (ILSP) was employed to prepare alginate polymers-based on natural polymers. ILSP achieved a remarkable 0-to-1 transformation in gaseous iodine adsorption, converting inactive alginic acid (∼0 g g−1 in saturated adsorption capacity) into a highly active iodine adsorbent (5.24 g g−1). It was revealed that electrophiles effectively regulated the electron cloud distribution of functional groups by replacing acidic protons on alginic acid, exerting a volumetric effect. This increased the electron density near the deprotonated carboxylic groups, enhancing the nucleophilicity of carboxylic groups. Consequently, it promoted halogen interaction between electron-rich oxygen atoms and iodine during adsorption, thereby improving the efficiency of charge transfer complex formation and polyiodide ion conversion. The ILSP strategy could provide guidance for the separation and conversion of gases such as iodine, carbon dioxide, and hydrogen.

A comparative study of Fe (II) doped chiral L/D-methionine carbon dots (MCDs) as a “Turn-on” fluorescent probe for the sensitive detection of L – cysteine

Chiral carbon dots have prominently influenced in the field of chemical, biological, and medicinal research. Comparing to achiral carbon dots, chiral carbon dots exhibit unique characteristics in biosensing application. In this perspective, we have developed bright blue, fluorescent L and d-Methionine Chiral carbon dots (MCDs) using a simple microwave assisted process for effective sensing of l-Cysteine. l-Cysteine plays a vital role in balancing the physiological redox in the body. These MCDs can be complexed with Fe2+ ions to create an energy transfer quenching system due to distinctive N and S functional group distribution on their surface. However, l-Cysteine attaches to Fe2+ ions in a competitive manner, leads to recovery of MCDs fluorescence. As a result, a "turn-on" fluorescent sensing platform based on L and d-Methionine-CDs has been developed for the rapid identification and detection of l-Cysteine. The probe shows good selectivity and sensitivity with coexisting biomolecules and ions. From comparative PL studies, d- MCDs are more responsive than l-Meth CDs towards the detection of l-cysteine with LOD of 0.71 µM and 0.94 µM respectively. The chiroptical properties were evaluated and the probe extends its practical application in paper strip and in biological matrix such as human blood serum with satisfactory recoveries in the range 85–104%.

Study of the high-energy alpha particles influence on the styrene accumulation kinetics and functional groups during the synthesis of proton-exchange membranes based on PVDF.

The study investigates the effect of alpha irradiation on the graft copolymerization of styrene with polyvinylidene fluoride (PVDF). Using methods of radiation-chemical modification, a proton exchange membrane (PEM) with a uniform distribution of functional sulfate groups throughout the entire volume was developed. Grafting of styrene was carried out at different temperatures and solution concentrations. Functional sulfo-groups were added to the graft polymer by sulfonation, with the addition of solvents. The degree of grafting (DG), water absorption (W) and exchange capacity (IEC) correlate well with the absorbed dose and alpha particle fluence. Research into this method will allow us to develop an affordable industrial technology for widespread implementation.

Nanoscale Spectroscopic Identification and Characterization of Minerals and Organic Matter in Ryugu Particles

AbstractCarbonaceous asteroids are leftover materials from the early solar system. They did not undergo planetary differentiation processes and thus still retained signatures and clues of the origin and evolution of the solar system. Thus, samples of carbonaceous asteroids provide significant potential for deciphering the origin of the solar system. The Hayabusa2 spacecraft returned the first samples of a carbonaceous asteroid (162173) Ryugu. In this work, we report the nanoscale mineralogy and organic matter content of two Ryugu particles, A0030 and C0034. These were analyzed by highly novel scattering‐type scanning near‐field optical microscopy (s‐SNOM)‐based nanoscale‐Fourier transform infrared (nano‐FTIR) spectroscopy with ∼20 nm spatial resolution. The nano‐FTIR measurements were supported by confocal micro‐Raman imaging and spectroscopy (∼500 nm/pixel spatial sampling). Our investigations show that the two Ryugu particles (a) contain different silicate mineralogies, indicating heterogeneous and incomplete aqueous alteration and (b) are highly rich in organic matter, consisting a variety of molecular functional groups. The spatial distributions of chemical functional groups and their associations based on pseudo‐heterodyne (PsHet) SNOM imaging show that the organic matter is distributed as either diffused or discrete grains. Micro‐Raman spectra show that the Ryugu particles experienced minimal thermal metamorphism, although A0030 was slightly more heated than C0034. The identification of abundant nanoscale organic molecules within the Ryugu grains that could not be identified via micrometer‐scale investigations emphasizes the importance of using nanoscale nondestructive methods for studying primitive solar system materials, such as Ryugu and OSIRIS‐Rex particles and those that will be returned in the future (such as MMX samples).

Visualization and Analysis of Mapping Knowledge Domains for Coal Functional Groups

ABSTRACT In this paper, a systematic review of the research on functional groups in coal is presented. In recent years, the research on functional groups in coal has been extended from the macroscopic level to the microscopic layer, and a large number of studies have shown that functional groups have significant effects on various properties of coal, such as gas adsorption and spontaneous combustion. To understand the current status and future trends of research on functional groups in coal, this study analyzed 3956 papers on this topic published in the Web of Science (WOS) core database from 2000 to 2022. The spatial and temporal distribution characteristics of publications, authors, countries, institutions, and major journals were visualized using VOSviewer and CiteSpace. Keyword co-occurrence and burst analysis are used to reveal the research status and hotspots in this field. The results show that the development of research on functional groups in coal goes through three stages: the fluctuating development period, the steady development period, and the results explosion period; China, USA, Australia, Japan, and India are the most active countries in the field of coal functional groups research, and China has a greater advantage in the number of publications and influence. A core group of institutions, mainly research universities, has been formed in this field, and Fuel, Energy and Fuels and Fuel Processing Technology are the main source journals for published results on coal functional groups. At present, the framework of basic theories and research methods is complete, and the study of functional groups for gas adsorption, the analysis of the evolution of functional groups in the process of coal thermodynamic behavior, and the characteristics of functional group categories and distribution in coal are the main knowledge framework basis for the study of functional groups in coal. The research on coal functional groups has been extended to the molecular level, and in the future, quantum chemistry, molecular simulation, and fine characterization research of functional groups will become the frontier of research in the field of coal functional groups.

Functional diversity and secondary production of macrofaunal assemblages can provide insights of biodiversity-ecosystem function relationships

BackgroundSemi-enclosed bays are important links in the material cycle and energy flow between terrestrial and marine ecosystems. They are also areas of intense human activities and heavily influenced by such activities as aquaculture, industrial and agricultural wastewater discharge. The rate of biodiversity loss and changes in ecosystems have prompted research into the relationship between species diversity and ecosystem functioning. Studies have shown that application of functional diversity indices is useful for assessing the status of ecosystem functioning. We quantitatively sampled macrofauna in a semi-enclosed bay in four seasons and analyzed the relationship between species, functional diversity and secondary production, biomass and feeding functional groups of macrofauna.ResultsThe annual secondary production was 325.01 kJ m−2 year−1. Detritivorous, carnivorous and planktophagous feeders were the main functional groups of macrofauna. Differences in the spatial–temporal distribution of functional groups were influenced by Ruditapes philippinarum and Hemileucon bidentatus. Functional richness had significant negative correlations with macrofaunal biomass and secondary production. Functional divergence, functional dispersion and Rao's quadratic entropy had highly significant negative correlations with macrofaunal biomass and secondary production.ConclusionThe results showed that high overlap of ecological niches can increase competition for habitat resources, leading to a decline in biomass and secondary production. In addition, aquaculture could promote the use of habitat resources to some extent, while it could increase competition for ecosystem resources (including habitat resources, atmospheric resources, water resources, etc.). Functional diversity is a good indicator for the ecosystem functioning and the competition status for habitat resources, which can provide insights into the current state of ecosystem function.

The impact of metal ions on flotation of coal gasification fine slag: an experimental study

ABSTRACT This study investigates the flotation performance of coal gasification fine slag in the presence of metal ions with different valences. The impact of metal ions on the surface topography, wettability, zeta potential, functional group, and particle size distribution of coal gasification fine slag were analyzed. The results demonstrated that K+, Ca2+, Mg2+, and Al3+ all have a positive effect on flotation, with Al3+ being particularly effective. At a concentration of 0.2 mol/L, Al3+ increased the recovery of combustible matter in coal gasification fine slag from 66.70% to 91.05% compared to deionized water. Metal ions reduce the absolute value of the gasification fine slag potential, compress its double layer while increasing its surface hydrophobicity. Higher ion concentration leads to a closer-to-zero potential and increased hydrophobicity. Additionally, Al3+ promote diesel adsorption onto coal gasification fine slag. This work explains the effects of metal ions on coal gasification fine slag flotation.

Janus Polyurethane Adhesive Patch with Antibacterial Properties for Wound Healing.

Despite the rapid development of tissue adhesives, flaws including allergies, poor stability, and indiscriminate double-sided adhesive properties limit their application in the medical field. In this work, Janus polyurethane patches were spontaneously prepared by adjusting the difference in the functional group distribution between the top and bottom sides of the patch during emulsion drying. Consequently, poor adhesion was exhibited on the bottom surface, while the top surface can easily adhere to metals, polymers, glasses, and tissues. The difference in adhesive strength to pork skin between the two surfaces is more than 5 times. The quaternary ammonium salt and hydrophilic components on the surface of the polyurethane patch enable the rapid removal and absorption of water from the tissue surface to achieve wet adhesion. Animal experiments have demonstrated that this multifunctional Janus polyurethane patch can promote skin wound closure and healing of infected wounds. This facile and effective strategy to construct Janus polyurethane patch provides a promising method for the development of functional tissue-adhesives.

Characterisation and double parallel random pore model fitting kinetic analysis of faulty coal oxygen-enriched co-combustion

This study used various analytical techniques to explore the structural characteristics of anthracite, lean coal, and bituminous coal. Thermogravimetric analysis assessed the combustion performance of individual coals and their blends. Results revealed distinct structural differences among the three coals. Although lean coal's functional groups distribution resembled bituminous coal, its carbon ordering aligned with anthracite. Increasing the proportion of bituminous coal minimally improved combustion in air. Under O2 + N2, rising oxygen levels lowered ignition and burnout temperatures, enhancing the comprehensive combustion index. At high heating rates, 30 %O2 + 70 %CO2 outperformed 30 %O2 + 70 %N2. The fitting performance of the double parallel random pore model (DRPM) was superior to that of the random pore model (RPM). Kinetic analysis suggested a DRPM for lean coal and bituminous coal co-combustion, unfolding in two stages. Activation energy increased with O2 concentration in O2 + N2 but remained lower than in O2 + CO2.

Effect of temperature on interface debonding behavior of graphene/graphene-oxide on cement-based composites

Temperature effect easily affect the adhesion of graphene/graphene oxide (GO) on the cement-based composites originating from the weaker non-covalent bonding at the interface, leading to weakening of the cementitious composite properties. In this study, the interfacial debonding behavior of graphene/GO and cement-based composites was investigated for low to high temperatures (250∼550 K) using controlled molecular dynamics simulations. The maximum tensile force and work of adhesion both decrease with increasing temperature, and the value of GO is 5∼6 times that of graphene. Especially at the high temperature end, GO is still difficult to peel off (Fmax: 7.93×103 pN, Wmax:2129.60 Kcal/mol). Meanwhile, the insights into the distribution and concentration of functional groups have shown that high concentrations and edge functional groups can improve interface adhesion. Energy decomposition demonstrated that, compared to the Coulomb effect of charge and the prestress of surface wrinkles, the van der Waals effect plays a major role in interface adhesion. Entropy analysis further reveals the high temperature sensitivity of graphene and the low sensitivity of GO due to edge functional groups. We believe that the insight into the temperature effect of interface debonding behavior at nanoscale can provide theoretical support for the effective temperature working conditions of graphene/graphene-oxide on cement-based composites.

Karst landforms as microrefugia for soil Collembola: Open versus forested dolines

Enclosed surficial karst dolines are geomorphologically diverse habitats with the potential to strongly shape community structure and the distribution of functional groups of organisms. Forest habitats in karst landscapes are characterized by lower soil temperatures and microclimatic fluctuations compared to open habitats; therefore, they may provide favorable conditions for cold-adapted/psychrophilic species, which are highly vulnerable to climate warming. We compared the diversity and structure of soil Collembola communities at sites along microclimatic gradients in open and forested karst dolines. The effect of topography and related environmental conditions on the distribution of ecological groups of soil Collembola was analyzed, and the function of the dolines as potential climate refugia for psychrophilic arthropods was assessed. The karst dolines revealed significant habitat heterogeneity, including warm plateaus and S-facing slopes and colder and wetter bottoms and N-facing slopes. The inner sites of the dolines had an overall higher abundance and species richness compared to the plateau sites. Nonmetric multidimensional scaling ordination revealed a clear delimitation of Collembola communities in terms of warmer and cooler sites in the open dolines, while the forested dolines did not reveal such a clear pattern. The studied dolines showed a potential to serve as microrefugia in the context of global climate change. Dolines could support the long-term persistence of at least some species such as cold-adapted species. Karst dolines in the temperate zone play a key role in maintaining biodiversity; therefore, they should be central in biodiversity conservation programs.

Alkali induced changes in spatial distribution of functional groups in carboxymethylated cellulose

The aim of the work was to investigate treatment parameters that exert most influence on performance of cellulose fibers carboxymethylated from aqueous solutions. Viscose fibers were carboxymethylated in alkaline solutions of sodium monochloroacetate at two temperatures (30 °C, 50 °C) and with different levels of alkali (0.5 mol/L and 4 mol/L NaOH). The degree of carboxymethylation was assessed with both back titration and conductometric titration methods, and the performance of carboxymethylated fibers was assessed from their propensity for sorption of the cationic dye methylene blue, a putative wastewater contaminant. Higher degrees of carboxymethylation were generally observed for fibers carboxymethylated in 4 mol/L NaOH, but in dye sorption propensities, the fibers carboxymethylated in 0.5 mol/L NaOH performed better. A combination of observations from dye sorption, color measurement and conductometric titration suggested that dye permeation was greater through fibers carboxymethylated in 0.5 mol/L NaOH as compared to 4 mol/L NaOH. As permeability differences were evinced in cases also where the degrees of carboxymethylation were very similar, it appears that the reaction conditions (i.e., alkali content during carboxymethylation), in addition to degree of carboxymethylation, affected fiber performance. The effect of alkali may stem from their influence on the topographical distribution of the substituted carboxymethyl functional groups.

Deep-sea benthic structures and substrate types influence the distribution of functional groups in the Wallaby-Zenith Fracture Zone (East Indian Ocean)

Three-dimensional deep-sea structures enhance substrate complexity and can shape numerous ecological hotspots that play critical roles in the diversity and distribution of benthic faunal assemblages. The characteristics of these features are not fully understood due to the logistical challenges of exploring at great depths and remote locations. One such deep-sea feature, the Wallaby-Zenith Fracture Zone (WZFZ) located in the East Indian Ocean, was mapped using a full-ocean depth multibeam echosounder system. Additionally, twelve baited landers and five crewed submersible dives were conducted in water depths between 4709 and 6591 m. We use seafloor bathymetry, bathymetric derivatives and video footage from the submersible dives to characterise the benthic structures, substrate types, habitat diversity, and the distribution of associated functional groups of megafauna for the WZFZ. The Benthic Terrain Modeler toolbox was used as an initial semi-automated step to generate benthic structural classes, which were further characterized through the inclusion of bottom salinity and temperature data collected by the scientific landers and integrated with the observations of seafloor substrate from the submersible video footage. This resulted in identification of nine benthic habitat classes characterised by unique seafloor morphological structure and substrate texture. A polymetallic nodule field, a possible extension of the previously reported Cape Leeuwen nodule field, was also observed along submersible transects conducted on the slopes of the WZFZ. The distribution and diversity of the functional megafauna groups observed are influenced by the deep-sea benthic habitats, defined by seafloor structures and substrate heterogeneity, especially the presence of hard substrates such as outcropping bedrock and polymetallic nodules within the WZFZ.

Investigation of physicochemical and chemical properties of biochar activated with carbonate, nitrate, and borohydride

AbstractActivation of biomass before pyrolysis with various chemicals significantly affects the surface area and porosity, chemical composition, and formation and distribution of functional groups on the surface of the biochar produced. For this purpose, raw tea waste (RTW) was mixed with potassium nitrate (KNO3), potassium sodium carbonate (NaKCO3), and sodium borohydride (NaBH4) in solid form and pyrolyzed at 500 °C for 1 h. The effects of the chemical activators on biomass char formation were investigated using DTA-TGA and DSC. Compared to conventional pyrolysis, carbonate, nitrate, and hydrides increase the gasification of biochar by catalyzing the decomposition of cellulose and lignin. The effect of NaBH4 on graphitization and deoxidation of carbon is higher than that of carbonates and nitrides. In addition, all prepared biochar samples were characterized by XRD, SEM, FT-IR, elemental analysis, and N2 adsorption–desorption. While treatment of RTW with KNO3 and NaKCO3 increased the hydroxylation of the biochar, treatment with NaBH4 decreased hydroxylation by increasing dehydrogenation and dehydroxylation. Increasing boron content led to hydroxylation of the material with hydratation of NaBO2. The surface area and pore distribution results showed that nitrates and carbonates have insignificant effect on the surface area of biochar, while NaBH4 almost doubles the surface area and total pore volume of biochar by forming hydrogen.

Hydrophilic 1T-WS2 Nanosheet Arrays toward Conductive Textiles for High-Efficient and Continuous Hydroelectric Generation and Storage.

Flexible hydroelectric generators (HEGs) are promising self-powered devices that spontaneously derive electrical power from moisture. However, achieving the desired compatibility between a continuous operating voltage and superior current density remains a significant challenge. Herein, a textile-based van der Waals heterostructure is rationally designed between conductive 1T phase tungsten disulfide@carbonized silk (1T-WS2@CSilk) and carbon black@cotton (CB@Cotton) fabrics with an asymmetric distribution of oxygen-containing functional groups, which enhances the proton concentration gradients toward high-performance wearable HEGs. The vertically staggered 1T-WS2 nanosheet arrays on the CSilk fabric provide abundant hydrophilic nanochannels for rapid carrier transport. Furthermore, the moisture-induced primary battery formed between the active aluminum (Al) electrode and the conductive textiles introduces the desired electric field to facilitate charge separation and compensate for the decreased streaming potential. These devices exhibit a power density of 21.6µWcm-2, an open-circuit voltage (Voc) of 0.65V sustained for over 10000s, and a current density of 0.17mAcm-2. This performance makes them capable of supplying power to commercial electronics and human respiratory monitoring. This study presents a promising strategy for the refined design of wearable electronics.

Catalytic Degradation of Lignin over Sulfonyl-Chloride-Modified Lignin-Based Porous Carbon-Supported Metal Phthalocyanine: Effect of Catalyst Concentrations.

A sulfonyl-chloride-modified lignin-based porous carbon-supported metal phthalocyanine catalyst was prepared and used to replace the traditional Fenton's reagent for lignin degradation. The catalyst underwent a detailed characterization analysis in terms of functional group distributions, surface area, morphological structure, via FT-IR, XPS, BET, and SEM. The catalyst possessed a specific surface area of 638.98 m2/g and a pore volume of 0.291 cm3/g. The prepared catalyst was studied for its ability of oxidative degradation of lignin under different reaction conditions. By optimizing the reaction conditions, a maximum liquid product yield of 38.94% was obtained at 135 °C with 3.5 wt% of catalyst and 15 × 10-2 mol/L H2O2; at the same time, a maximum phenols selectivity of 32.58% was achieved. The compositions and properties of liquid products obtained from lignin degradation using different catalyst concentrations were studied comparatively via GC-MS, FT-IR, 1H-NMR, and EA. Furthermore, the structure changes of solid residues are also discussed.

Distribution of oxygen-containing functional groups on defective graphene: properties engineering and Li adsorption.

In this study, the distribution of oxygen-containing functional groups on graphene with vacancies and topological defects was systematically investigated using advanced computational methods and the structure models for multi-defect graphene oxides (GOs) were proposed. All potential adsorption sites were considered through an automated structure generation program to identify energetically favorable structures. Unlike the pristine graphene surface where oxygen-containing functional groups always aggregate with each other, we observed a tendency for them to preferentially adsorb near defects. Furthermore, they may also be distributed on the same side or both sides of the defective graphene. These multi-defect GOs can exhibit either metallic or semiconducting properties. Notably, upon adsorbing the same oxygen-containing functional groups onto the surface of defective graphene, their electronic characteristics become homogeneous. The coexistence of vacancy/topological defects and oxygen-containing functional groups within the graphene lattice introduces intriguing mechanical anisotropic properties to graphene, including the uncommon negative Poisson's ratio. Additionally, these materials exhibit anisotropic optical behavior, displaying heightened absorption within the infrared and visible regions compared to pristine graphene. Finally, it is found that Li atoms are adsorbed stably on the surfaces of multi-defect GOs via the formation of LinO/LimOH clusters. The research findings presented in this paper, encompassing the development of structural models for multi-defect GOs, could provide crucial insights into the properties and potential applications of graphene oxides.

Performance and application of PS slow-release algal inhibition materials based on modified fly ash and cement

In this paper, a new type of slow-release algae control agent was prepared by using modified fly ash and cement as the base material and PS (potassium persulfate), an inorganic substance that dissolves algae by destroying their cellular structure, as the active component, and compounding the three in a certain proportion, and the finished product was obtained after 14 days of maintenance. The rate of release is primarily influenced by temperature, particle size, and load, while pH has minimal impact. Specifically, as the temperature increases from 4 °C to 40 °C, the rate of slow release increases from 0.74 mg/g/d to 1.35 mg/g/d. When particle size increased from 3 mm to 5 mm, the slow-release rate decreased from 1.06 mg/g/d to 0.70 mg/g/d. When the load increased from 10 mg/g to 30 mg/g, the slow-release rate also increased from 0.60 mg/g/d to 2.10 mg/g/d. In the algal inhibition experiment, the composite material was selected with a dose of 20 g/L, a loading capacity of 15 mg/g, and a particle size of 3 mm. After 14 days, algae removal rates, ammonia nitrogen, total phosphorus, and COD were found to be 96.55 %, 56.14 %, 78.2 %, and 86.81 %, respectively. The microstructure, elemental composition, and distribution of functional groups in the materials were analyzed using SEM, EDS, and FTIR. The algal suppressor was evenly distributed throughout the substrate surface. Additionally, there was a decrease in metal elements and an increase in hydroxyl groups. The experimental data show that the material is a slow-release algal inhibitor with good performance and practical application value.