Metal Hydroxides Research Articles

A facile route for decoration of hematite photoanodes by transition metal hydroxide co‐catalysts

AbstractEarth‐abundant α‐Fe2O3 (hematite) is a convincing photoanode for photoelectrochemical (PEC) water splitting; however, its intrinsic properties of inferior charge transfer and sluggish water oxidation kinetics limit its performance. Here, we report a straightforward decoration method for transition metal hydroxides to accelerate the oxygen evolution reaction (OER) of hematite photoanodes grown by electric field‐assisted liquid phase deposition (EA‐LPD). The investigations revealed that Co(OH)2 acts as a superior co‐catalyst compared with hydroxides of Mn, Fe, Co, Ni, and Zn. EA‐LPD‐grown hematite photoanode loaded with cobalt hydroxide exhibited an excellent PEC performance. A photocurrent density of 0.93 mA.cm−2 at 1.23 V versus reversible hydrogen electrode was achieved for the modified hematite, ∼3 times more than that of pristine hematite, and a cathodic shift of 100 mV for the onset potential was observed. The proposed simple and cost‐effective co‐catalyst loading strategy provides a high degree of freedom in the design of co‐catalysts with a complex chemical composition comprising transition metal oxyhydroxides and hydroxides on different photoanodes for more efficient charge carrier separation for the PEC applications.

Hierarchical Cu3V2O8/Cu6Mo5O18/MXene nanostructures by ultrathin nanosheets for highly sensitive electrochemical detection of organophosphorus pesticides

Transition-metal oxides (TMOs) with hierarchical nanostructures derived from metal organic frameworks (MOFs) were widely applied in electrochemical investigation. In this paper, a rational synthesis strategy of TMOs with specific nanostructures and multiple components was reported. Three-dimensional (3D) CuMoV layered metal hydroxides (CuMoV LDHs) architecture was prepared by mild and facile wet-chemistry process to reshape Cu-MOF surface and realize the self-templated conversion. After thermal annealing, hierarchical CuMoV LDHs were transformed to polynary Cu3V2O8/Cu6Mo5O18 (CMVO) compounds. Based on the electrostatic attraction, CMVO/MXene (CMVON) compounds were assembled by combining the CMVO and few-layer Nb2CTx MXene (f-Nb2C) nanosheets and employed as modified materials on the electrode surface. Benefiting from the superior electronic conductivity, large surface area and shortened ion diffusion pathway, the CMVON hybrids demonstrated excellent electrochemical sensing properties. Upon optimum conditions, the constructed CMVON based AChE biosensor manifested markedly analytical performance with the low limit of detection (LOD) and wide linear ranges for parathion-methyl, malathion, and fenitrothion detection.

A DFT study of the adsorption of fouling molecules (metal sulfides and hydroxides) onto TiZrO4 ceramic membranes

Ceramic membrane fouling is a constraint in the treatment of acid mine drainage (AMD), leading to a decrease in efficiency over time. Here, it is described via first-principles calculations the physical and chemical phenomena occurring on the surface of TiZrO4 filtration membranes due to the adsorption of eight potential fouling compounds [CuS, FeS, Fe2S3, CaS, Al(OH)3, Fe(OH)3, Fe(OH)2, and Cu(OH)2]. The interaction of these fouling molecules was performed onto nanostructured TiZrO4 surfaces with several pores representing the filtration membranes employed in the treatment of AMD. The adsorption energies reveal that the adsorption is feasible with all the fouling molecules studied, and it is strongly related to the molecular polarity of the adsorbate. Consequently, the adsorption of metal sulfides is more feasible than hydroxides with adsorption orders of CaS>FeS>CuS>Fe2S3, and Al(OH)3>Fe-hydroxides>Cu(OH)2. The outcomes suggest that the metal sulfide adsorption depends on the adsorbate intrinsic polarity, solvent effects, adsorbate van der Waals radius, and membrane surface topology, while the adsorption of hydroxides is less influenced by the last two factors. Density-based binding and energy decomposition analyses indicate strong electrostatic attractions and covalent bonds at the adsorbate-membrane interface supporting the chemical fouling onto ceramic filtration membranes. According to our theoretical results and the elevated concentration of Cu and Fe in AMD, we propose that FeS and CuS are mainly responsible for the fouling onto TiZrO4 membrane surfaces. These results offer valuable information on the adsorption phenomena at TiZrO4 membrane surfaces, which can be useful for metallurgy, industrial water treatment, food industry, biotechnology, and pharmaceutical applications.

Structure, Properties, and Preparation of MXene and the Application of Its Composites in Supercapacitors

Two-dimensional transition metal carbides/nitrides (MXenes) are emerging members of the two-dimensional material family, obtained by removing the A layer of the MAX phase through methods such as liquid-phase etching. This article summarizes the structure and properties of MXenes, as well as several preparation methods, including etching with hydrofluoric acid and fluoride salts, alkali-based etching, electrochemical etching, Lewis acid molten salt etching, and direct synthesis. Due to their unique two-dimensional structure and surface chemistry, MXenes exhibit good metallic conductivity, hydrophilicity, excellent flexibility, and ion intercalation properties, showing great potential in the research and application of supercapacitors and attracting widespread attention. The combination of MXene with other types of materials, including polymers, metal hydroxides, metal oxides, and carbon materials, takes advantage of composites to improve energy storage performance and shows great potential in the research and application of supercapacitors. This article provides a detailed summary of MXene composite materials and capacitor performance and introduces the research progress of MXene materials in the field of supercapacitor energy storage applications, aiming to provide references for the preparation of high-performance MXene supercapacitor electrode materials.

Efficient phosphate removal by Mg-La binary layered double hydroxides: synthesis optimization, adsorption performance, and inner mechanism.

Layered double hydroxides (LDH) hold great promise as phosphate adsorbents; however, the conventional binary LDH exhibits low adsorption rate and adsorption capacity. In this study, Mg and La were chosen as binary metals in the synthesis of Mg-La LDH to enhance phosphate efficient adsorption. Different molar ratios of Mg to La (2:1, 3:1, and 4:1) were investigated to further enhance P adsorption. The best performing Mg-La LDH, with Mg to La ratio is 4:1 (LDH-4), presented a larger adsorption capacity and faster adsorption rate than other Mg-La LDH. The maximum adsorption capacity (87.23 mg/g) and the rapid adsorption rate in the initial 25 min of LDH-4 (70 mg/(g·h)) were at least 1.6 times and 1.8 times higher than the others. The kinetics, isotherms, the effect of initial pH and co-existing anions, and the adsorption-desorption cycle experiment were studied. The batch experiment results proved that the chemisorption progress occurred on the single-layered LDH surface and the optimized LDH exhibited strong anti-interference capability. Furthermore, the structural characteristics and adsorption mechanism were further investigated by SEM, BET, FTIR, XRD, and XPS. The characterization results showed that the different metal ratios could lead to changes in the metal hydroxide layer and the main ions inside. At lower Mg/La ratios, distortion occurred in the hydroxide layer, resulting in lower crystallinity and lower performance. The characterization results also proved that the main mechanisms of phosphate adsorption are electrostatic adsorption, ion exchange, and inner-sphere complexation. The results emphasized that the Mg-La LDH was efficient in phosphate removal and could be successfully used for this purpose.

Layer-by-layer growth of Cu3(HHTP)2 films on Cu(OH)2 nanowire arrays for high performance ascorbic acid sensing

Growing three-dimensional (3D) metal organic frameworks (MOFs) via heterogeneous epitaxial growth on metal hydroxide arrays are effective for constructing electrochemical sensor. However, the growth of MOFs is difficult to control, resulting in thick and irregular morphologies and even damage the metal hydroxide template. In this work, Cu3(HHTP)2 (HHTP = 2, 3, 6, 7, 10, 11-hexahydroxytriphenylene) films with controllable thickness and morphology were successfully prepared on Cu(OH)2 nanowire arrays (NWAs) through layer-by-layer (LBL) growth method. We have discovered that the LBL cycle and the reaction solvent composition are crucial for growing homogenous MOF thin films. The Cu3(HHTP)2 based ascorbic acid (AA) sensor, fabricated in ethanol within 10 LBL cycles, generated an ultrahigh sensitivity of 821.64 μA mM−1 cm−2 in the range of 6–981.41 μM, a low detection limit of 60 nM as well as the great selectivity, stability and reproducibility. Moreover, the relative deviation for AA detection in two fruit juices were 3.22 % and 3.71 %, and the test result for human sweat fall within the normal AA concentration range, verifying the feasibility of as-prepared sensor for practical application.

Differential surface modification mechanism of chalcopyrite and pyrite by Thiobacillus ferrooxidans and its response to bioflotation

Mineral processing encounters the challenge of separating chalcopyrite and pyrite, with the conventional high alkali process characterized by issues such as large dosages of reagents, complex procedures, and environmental pollution. This study addresses this challenge by isolating and enriching Thiobacillus ferrooxidans (T·f) from acidic mine drainage, employing it as a biosurfactant. The modification mechanism of T·f was thoroughly analyzed. Fe dissolution through biological oxidation formed a passivation layer (jarosite [KFe3(SO4)2(OH)6], elemental sulfur (S0), and metal sulfides (Cu/Fe–S) on the surface of minerals. Metal oxides, hydroxides, and sulfates were detected on the surface of two minerals, but the difference was that elemental sulfur (S0) and copper sulfide (Cu-S) were detected on the surface of chalcopyrite. elucidating the fundamental reason for the significant difference in surface hydrophobicity between chalcopyrite and pyrite. T·f has been successfully used as a biosurfactant to achieve copper-sulfur separation.

The Sensitivity of Structure to Ionic Radius and Reaction Stoichiometry: A Crystallographic Study of Metal Coordination and Hydrogen Bonding in Barbiturate Complexes of All Five Alkali Metals Li-Cs.

A systematic study has been conducted on barbiturate complexes of all five alkali metals, Li-Cs, prepared from metal carbonates or hydroxides in an aqueous solution without other potential ligands present, varying the stoichiometric ratio of metal ion to barbituric acid (BAH). Eight polymeric coordination compounds (two each for Na, K, and Rb and one each for Li and Cs) have been characterised by single-crystal X-ray diffraction. All contain some combination of barbiturate anion BA- (necessarily in a 1:1 ratio with the metal cation M+), barbituric acid, and water. All organic species and water molecules are coordinated to the metal centres via oxygen atoms as either terminal or bridging ligands. Coordination numbers range from 4 (for the Li complex) to 8 (for the Cs complex). Extensive hydrogen bonding plays a significant role in all the crystal structures, almost all of which include pairs of N-H···O hydrogen bonds linking BA- and/or BAH components into ribbons extending in one dimension. Factors influencing the structure adopted by each compound include cation size and reaction stoichiometry as well as hydrogen bonding.

COMPARATIVE THERMAL KINETIC ANALYSIS OF NICKEL HYDROXIDE NANOPARTICLES THROUGH CHEMICAL PRECIPITATION AND SOL–GEL ROUTES

In most of the chemical methods, the as-prepared NPs have a metal hydroxide form. The calcination temperature is very important to prepare the metal oxide from metal hydroxide. Thus, in this work, the chemical precipitation and sol–gel routes were employed to produce the Nickel hydroxide nanoparticles and analyze their functional, structural, thermal, and morphological behavior of prepared NPs. The formation of Ni(OH)2 is confirmed by FTIR analysis including both techniques. Rietveld refinement techniques were used to diffraction patterns by the program FullProf. The well-matched XRD patterns reveal that prepared NPs have [Formula: see text]-Ni(OH)2 phase and hexagonal structure (HCP) with a space group of P3m1 for both the methods. The kinetic factors were calculated using different models. The Phadnis–Deshpande model is employed to identify the mechanism of solid state kinetic reaction. Solid state kinetic model observes nucleation and nuclei growth (Avrami–Erofeev nuclei growth) and 2D diffusion mechanism for chemical precipitation and sol–gel, respectively. From the FESEM analysis, flower-shaped architectures and nanosheet morphology are presented in the prepared sample by chemical precipitation and sol–gel, respectively. From the kinetic parameters, we conclude that the decomposition of Ni(OH)2 to NiO is thermally stable, has slow reaction and spontaneous process at 300∘C. The results show that the chemical precipitation method is more suitable for energy storage application compare to the Sol–gel method.

MOF-Mediated Construction of NiCoMn-LDH Nanoflakes Assembled Co(OH)F Nanorods for Improved Supercapacitive Performance.

The application of transition metal hydroxides has long been plagued by its poor conductivity and stability as well as severe aggregation tendency. In this paper, a novel hierarchical core-shell architecture, using an F-doped Co(OH)2 nanorod array (Co(OH)F) as the core and Mn/Ni co-doped Co(OH)2 nanosheets (NiCoMn-LDH) as the shell, was constructed via an MOF-mediated in situ generation method. The obtained Co(OH)F@ NiCoMn-LDH composites exhibited excellent supercapacitive performance with large specific capacitance as well as improved rate capability and long-term stability. The effect of the Ni/Mn ratio on the supercapacitive performance and energy storage kinetics was systematically investigated and the related mechanism was revealed.

The Chemistry of Spinel Ferrite Nanoparticle Nucleation, Crystallization, and Growth.

The nucleation, crystallization, and growth mechanisms of MnFe2O4, CoFe2O4, NiFe2O4, and ZnFe2O4 nanocrystallites prepared from coprecipitated transition metal (TM) hydroxide precursors treated at sub-, near-, and supercritical hydrothermal conditions have been studied by in situ X-ray total scattering (TS) with pair distribution function (PDF) analysis, and in situ synchrotron powder X-ray diffraction (PXRD) with Rietveld analysis. The in situ TS experiments were carried out on 0.6 M TM hydroxide precursors prepared from aqueous metal chloride solutions using 24.5% NH4OH as the precipitating base. The PDF analysis reveals equivalent nucleation processes for the four spinel ferrite compounds under the studied hydrothermal conditions, where the TMs form edge-sharing octahedrally coordinated hydroxide units (monomers/dimers and in some cases trimers) in the aqueous precursor, which upon hydrothermal treatment nucleate through linking by tetrahedrally coordinated TMs. The in situ PXRD experiments were carried out on 1.2 M TM hydroxide precursors prepared from aqueous metal nitrate solutions using 16 M NaOH as the precipitating base. The crystallization and growth of the nanocrystallites were found to progress via different processes depending on the specific TMs and synthesis temperatures. The PXRD data show that MnFe2O4 and CoFe2O4 nanocrystallites rapidly grow (typically <1 min) to equilibrium sizes of 20-25 nm and 10-12 nm, respectively, regardless of applied temperature in the 170-420 °C range, indicating limited possibility of targeted size control. However, varying the reaction time (0-30 min) and temperature (150-400 °C) allows different sizes to be obtained for NiFe2O4 (3-30 nm) and ZnFe2O4 (3-12 nm) nanocrystallites. The mechanisms controlling the crystallization and growth (nucleation, growth by diffusion, Ostwald ripening, etc.) were examined by qualitative analysis of the evolution in refined scale factor (proportional to extent of crystallization) and mean crystallite volume (proportional to extent of growth). Interestingly, lower kinetic barriers are observed for the formation of the mixed spinels (MnFe2O4 and CoFe2O4) compared to the inverse (NiFe2O4) and normal (ZnFe2O4) spinel structured compounds, suggesting that the energy barrier for formation may be lowered when the TMs have no site preference.

Dual role of sulfur doping in NiCr LDH for water oxidation: Promoting surface reconfiguration and lattice oxygen oxidation

Heterogeneous doping is widely applied to improve the oxygen evolution reaction (OER) activity of layered double metal hydroxides (LDH), but it is challenging to study the reconfiguration and reaction mechanism of catalysts. Herein, we prepared sulfur-doped NiCr LDH (Sx-NiCr LDH) pre-catalyst, which exhibits low overpotential of 244.4 mV at 100 mA cm−2 after reconfiguration. The characterization results reveal that sulfur doping not only optimizes the reconfiguration process of NiCr LDH by modulating Cr leaching, but also reduces the oxidation potential of Ni2+. Density functional theory (DFT) results show that sulfur doping reduces the energy barrier of reconfiguration, enhances the covalency of Ni-O, and upshifts the O 2p band center to promote lattice oxygen oxidation. The reconfigured catalyst requires 1.51 and 1.47 V at 10 mA cm−2 for overall water splitting at 25 °C and 80 °C, respectively. This work provides a valuable approach for designing highly active LDH catalysts.

Nickel Hydroxide-Based Electrocatalysts for Promising Electrochemical Oxidation Reactions: Beyond Water Oxidation.

Transition metal hydroxides have attracted significant research interest for their energy storage and conversion technique applications. In particular, nickel hydroxide (Ni(OH)2), with increasing significance, is extensively used in material science and engineering. The past decades have witnessed the flourishing of Ni(OH)2-based materials as efficient electrocatalysts for water oxidation, which is a critical catalytic reaction for sustainable technologies, such as water electrolysis, fuel cells, CO2 reduction, and metal-air batteries. Coupling the electrochemical oxidation of small molecules to replace water oxidation at the anode is confirmed as an effective and promising strategy for realizing the energy-saving production. The physicochemical properties of Ni(OH)2 related to conventional water oxidation are first presented in this review. Then, recent progress based on Ni(OH)2 materials for these promising electrochemical reactions is symmetrically categorized and reviewed. Significant emphasis is placed on establishing the structure-activity relationship and disclosing the reaction mechanism. Emerging material design strategies for novel electrocatalysts are also highlighted. Finally, the existing challenges and future research directions are presented.

Advances of Layered Double Hydroxide-Based Materials for Tumor Imaging and Therapy.

Layered double hydroxides (LDH) are a class of functional anionic clays that typically consist of orthorhombic arrays of metal hydroxides with anions sandwiched between the layers. Due to their unique properties, including high chemical stability, good biocompatibility, controlled drug loading, and enhanced drug bioavailability, LDHs have many potential applications in the medical field. Especially in the fields of bioimaging and tumor therapy. This paper reviews the research progress of LDHs and their nanocomposites in the field of tumor imaging and therapy. First, the structure and advantages of LDH are discussed. Then, several commonly used methods for the preparation of LDH are presented, including co-precipitation, hydrothermal and ion exchange methods. Subsequently, recent advances in layered hydroxides and their nanocomposites for cancer imaging and therapy are highlighted. Finally, based on current research, we summaries the prospects and challenges of layered hydroxides and nanocomposites for cancer diagnosis and therapy.

Methods for obtaining humate-containing fertilizers from brown coal

ABSTRACT The purpose of the study is to examine the main methods of obtaining fertilizers and optimizing processes. Using methods of analysis, comparison, and experimentation, three main approaches to obtaining fertilizers were identified: grinding and mixing with potassium hydroxide (KOH), ultrafine grinding with chemical additives, and a complex method for processing caustobioliths. Comparative analysis of the investigated methods allowed for identifying their advantages, disadvantages, and effectiveness. The key result was the ability to determine the most effective method for producing humate-containing fertilizers from brown coal, depending on specific production conditions and requirements. The results of the study showed that the ultrafine grinding process with chemical additions, such as urea and alkali metal hydroxides, showed promising potential for creating highly effective humate-containing fertilizers from brown coal, in addition to the comparative analysis. After thorough optimization, this technique showed improved fertilizer utilization and superior plant uptake, making it a strong contender for sustainable farming methods. Nevertheless, achieving optimal results requires detailed process parameter optimization. The study underscores the importance of using brown coal in humate-containing fertilizer production as an environmentally safe and sustainable approach. The results can contribute to further development and improvement of humate-containing fertilizer production methods, promoting sustainable agriculture and increased crop productivity.

Binary NiCu oxide nanoparticles onto graphite as promoting nanocatalysts for ethanol electro‐oxidation process

A facile and reduced cost fabrication protocol was followed to have a series of nickel oxide nanospecies onto graphite support with introducing varied copper oxide wt.% values (NiCuO/T). The co‐precipitation of metallic hydroxide particles onto carbonaceous surfaces and their subsequent burning at 400°C were sufficient to prepare mixed transition metal oxides. Suitable analysis tools were exploited to fully characterize the obtained nanopowders using scanning electron microscopy, transmission electron microscopy, X‐ray diffraction spectroscopy, X‐ray photoelectron spectroscopy, and energy dispersive X‐ray analysis. Outstanding performances of the formed nanocatalysts for catalyzing ethanol electro‐oxidation reaction were measured especially in presence of 15 wt.% copper oxide content. The onset potential (Eonset) value of alcohol oxidation process was negatively shifted at dispersed NiO nanoparticles onto graphite after doping with copper oxide nanospecies. This promoted activity of prepared nanomaterials could be explained by their increased active sites when binary metallic oxides were incorporated. Electrochemical impedance spectroscopy studies demonstrated much lowered resistances in alkaline solution containing ethanol molecules to ascertain the enhanced behavior of NiCuO/T nanocatalysts. Moreover, their good stability attitude encouraged the application of doped nanomaterials with copper oxide for fuel cells application.

Enriched supercapacitive performance of electrochemically tailored β-Co(OH)2/CoOOH nanodiscs from sacrificial Co3(PO4)2·4H2O microbelts

Electrochemically induced structural reconstruction process of metal precursors into their corresponding metal hydroxides/(oxy)hydroxides is developed as an ingenious strategy towards preparing efficient electrode material. However, the influence of electrochemical activation on the charge storage ability of electrode material is barely explored. Herein, we have utilized a synthetic strategy (solvothermal reaction in water:ethanol mixture) to prepare Co3(PO4)2·4H2O microbelts and subsequently applied the electrochemical bulk reconstruction process in 1 M KOH electrolyte. A thorough physical and electrochemical characterization unveil that the electrode material is converted into redox active site rich β-Co(OH)2/CoOOH nanodiscs via etching of lattice anionic PO43− moieties. The material possesses a specific capacitance of 386 F g−1at a current density of 0.25 A g−1. Additionally, a hybrid device constructed with β-Co(OH)2/CoOOH nanodiscs and activated charcoal (AC) as positive and negative electrodes has achieved a high energy density of 13.33 Wh Kg−1at a power density of 400 W kg−1. Further, the device displayed a good capacitance retention of 93 % (columbic efficiency ~98 %) up to 10,000 cycles. The improved charge storage of reconstructed material with abundant redox active sites could be attributed to the facile diffusion of electrolyte ions into the bulk of the material.

Design of Functional Materials Using Organic–Inorganic Hybrid Metal Hydroxide Salts Nanoparticles

Design of Functional Materials Using Organic–Inorganic Hybrid Metal Hydroxide Salts Nanoparticles

Oxygen Vacancy and Heterostructure Modulation of Co2P/Fe2P Electrocatalysts for Improving Total Water Splitting.

Designing a stable and highly active catalyst for hydrogen evolution and oxygen evolution reactions (HER/OER) is essential for the industrialization of hydrogen energy but remains a major challenge. This work reports a simple approach to fabricating coupled Co2P/Fe2P nanorod array catalyst for overall water decomposition, demonstrating the source of excellent activity in the catalytic process. Under alkaline conditions, Co2P/Fe2P heterostructures exhibit an overpotential of 96 and 220 mV for HER and OER, respectively, at 10 mA cm-2. For total water splitting, a low voltage of 1.56 V is required to provide a current density of 10 mA cm-2. And the catalyst exhibits long-term durability for 30 h at a high current density of 250 mA cm-2. The analysis of the results revealed that the presence of interfacial oxygen vacancies and the strong interaction between Co2P/Fe2P provided the catalyst with more electrochemically active sites and a faster charge transfer capability, which improved the hydrolysis dissociation process. Electrochemically active metal (oxygen) hydroxide phases were produced after OER stability testing. The results of this study prove its great potential in practical industrial electrolysis and provide a reasonable and feasible strategy for the design of nonprecious metal phosphide electrocatalysts.

Development of Fire Resistant Composite Material Using Fire Retardant Filler for Electrical Application

Safety is paramount across diverse sectors, with a growing emphasis on dependability. Preventing fires in electrical contexts and employing fire-resistant techniques using additives have become crucial. This involves the development of composite materials, typically incorporating substances like Alumina Rehydrate (ATH), metal hydroxides, or specialized additives such as epoxies, polyester, or polyurethane resins within polymer matrices. These formulations include fire-retardant fillers, underscoring their significance in enhancing safety and reliability. Increasing the fire resistance of the composite can be achieved through various methods such as delaying ignition, reducing flame spread, mitigating smoke emissions when exposed to high temperatures, and employing fire-resistant compounds to quench potential electrical arcs, especially in electrical applications where combustible materials pose significant hazards. These items consist of electrical casings, wire pathways, insulation, and other crucial components for ensuring fire safety within various systems. These components are chosen based on their electrical characteristics, strength, and the necessity for fire resistance, all of which contribute to achieving a harmonious balance. Careful consideration is given to adhesive matrices during the selection and optimization process as part of the development procedure. Advanced manufacturing methods such as Compression Melding, Resin Transfer Melding, or filament winding are utilized to produce composite components with standardized properties, enhancing overall efficiency.