Removal Mechanism Research Articles

A multifunctional coconut shell biochar modified by titanium dioxide for heavy metal removal in water/soil and tetracycline degradation

Heavy metals and tetracycline pollute the environment and endanger human health. This work prepared a multifunctional coconut shell biochar (Ti-XBC) through NaHCO3 activation and TiO2 modification. The modified coconut shell biochar was characterized by various methods. Ti-4BC exhibited excellent removal performance for heavy metals. The maximum adsorption capacity of Ti-4BC on Cd2+, Pb2+, Cr3+, and Cr6+ reached 104.2, 136.8, 101.2, 112.4 mg/g in water. The adsorption of Ti-4BC for four metal ions had a competitive effect in the binary metal system. It also reduced the mobility of four heavy metal ions in soil. Density functional theory (DFT) calculations were employed to explain the mechanism of heavy metal removal. Additionally, the degradation performance and mechanism of Ti-4BC towards tetracycline were investigated. The results indicated that the maximum degradation rate was 99.4%. Overall, this work developed a multifunctional material capable of both removing heavy metals and degrading antibiotics, addressing the issue of single-function in biochar. This provided a novel approach for tackling complex and diverse environmental pollution scenarios.

Acquired blaCfxA-3 carried by a conjugative transposon or duplicated intrinsic blaCME-3 mediates cefiderocol resistance in Elizabethkingia anophelis clinical isolates

ObjectivesElizabethkingia spp. are resistant to multiple antibiotics. This study aimed to determine in vitro and in vivo activities of cefiderocol against Elizabethkingia spp. and to investigate resistance mechanisms. MethodsBloodstream isolates were collected from four hospitals. In vitro and in vivo activities were determined using broth microdilution and the wax moth model, respectively. Genome comparison and gene editing were used to confirm the contribution of target genes. Conjugation experiments and serial passage were used to determine transferability and stability, respectively. A MIC of ≤ 4 mg/L was designated as the susceptibility breakpoint. ResultsAmong 228 non-duplicated isolates, 226 exhibited a MIC of ≤ 4 mg/L with MIC50/90 of 1/2 mg/L. Two isolates had a MIC of 128 mg/L; both source patients had multiple comorbidities, were ventilator-dependent, and had not received cefiderocol previously. Resistance was attributable to acquisition of blaCfxA-3, carried by a conjugative transposon from Prevotella jejuni, and duplication of intrinsic blaCME-3, which led to its overexpression. tetQ coexisted with blaCfxA-3 in this conjugative transposon and minocycline facilitated its transfer among E. anophelis. Antibiotics prescribed for source patients did not induce blaCME-3 duplication. The stabilities of blaCfxA-3 and double blaCME-3 were 100% and > 90%, respectively, after 10-day serial passage. Cefiderocol failed to rescue moth larvae infected with resistant strains, but removal of resistance mechanisms restored in vivo efficacy. ConclusionsCefiderocol was in vitro and in vivo active against Elizabethkingia spp. but resistance may emerge due to the availability, transferability, and/or stability of resistance mechanisms.

Atomic-scale material removal and deformation mechanism in nanoscratching GaN

Gallium nitride (GaN) is an important third-generation semiconductor material. However, due to its high hardness, high brittleness and anisotropy, the material removal efficiency of GaN during ultraprecision machining is low, and subsurface damage easily occurs. In order to achieve high-efficiency and low-damage ultra-precision machining, the model of double nanoscratches is innovatively utilized to investigate the mechanical behavioral of GaN at the atomic scale. Specifically, double nanoscratches experiments and corresponding molecular dynamics (MD) simulations were carried out on GaN (0001) crystal plane along the [101¯0] and [12¯10] crystal directions to reveal the material removal, deformation and subsurface damage mechanisms of GaN under anisotropic conditions. The results show that the plastic removal of GaN can be realized by setting loading force and scratch spacing. Scratching along the [12¯10] crystal direction has a greater ductile-brittle transition load force than the [101¯0] crystal direction. MD analysis shows that the downward-extending prismatic slip produced by scratching along the [101¯0] crystal direction is the cause of crack extension to the subsurface during the experiment. As the load force increases, the surface cracks of the double scratches expand and intersect, inducing streak-like brittle fracture. The significant increase in the lateral force of the second scratch is the main reason for the brittle fracture in the double scratch experiment. After the double nanoscratches experiment, the damage presented on the GaN subsurface mainly includes atomic scale damage such as amorphization, stacked laminations, polycrystalline nanoscratch, and phase transition. The Stacking fault bands around the damage zone inhibit the damage extension. The second scratch generates a large number of dislocations in the overlap zone and attenuates the subsurface amorphization under the influence of dislocation strengthening effect.

Endovascular thrombectomy for distal medium vessel occlusions: A literature review

BackgroundThere is a lack of substantial evidence supporting the safety and effectiveness of endovascular thrombectomy in treating distal medium vessel occlusions (DMVOs). ObjectiveTo summarize the current evidence regarding endovascular thrombectomy for DMVOs. MethodsWe conducted a narrative review of key articles related to the diagnosis and management of DMVOs. We manually searched PubMed and Google Scholar from January 2010 to July 2023, and only included articles published in the English language. ResultsWhile diagnosing and treating DMVOs is tricky due to access limitations and potential limited benefit from mechanical clot removal, recent improvements in catheter and retrieval technology suggest that endovascular thrombectomy might be a potential treatment option. However, more high-quality research is needed to confirm its effectiveness for DMVOs. ConclusionExperts disagree on how to classify DMVOs and what the best mode of endovascular treatment is.

Efficient recovery of Pd(II) from nuclear wastewater using a functionalized covalent organic frameworks with uniform spherical structure: Size control, performance and mechanism insight

The efficient recovery of palladium from the spent nuclear fuel was of great significance to the sustainable development of nuclear energy. Herein, the uniform spherical COFs were constructed by a facile approach at room temperature, which were further surface functionalized by a thiol-ene “click” reaction to recover Pd(II). Microscopic and spectroscopic studies manifested that the formation mechanism and size of spherical COFs were greatly affected by the amount of catalyst and solvent type. The TAPB-BPTA-DTT and TAPB-BPTA-S-β-CD exhibited high Pd(II) recovery efficiency due to the introduction of sulfhydryl groups, and the maximum adsorption capacities were 489.3 and 234.3 mg/g, respectively. Meanwhile, the water environmental condition played an important role in the separation process, and the classical adsorption models demonstrated that monolayer chemisorption was the dominant removal mechanism. Mechanism analysis showed that the excellent adsorption performance was mainly attributed to the electrostatic interaction, physical absorption and chelation of N, O, and S groups with Pd(II). Thus, it is expected that this work could provide more insight into COFs materials, thereby promoting palladium removal advancements in the spent nuclear fuel.

Enhanced removal of Fe, Cu, Ni, Pb, and Zn from acid mine drainage using food waste compost and its mechanisms

Heavy metals (HMs) in acid mine drainage (AMD) pose serious threats to aquatic life and soil. Biosorbents are promising materials to remove HMs from wastewater. Herein, food waste compost was used as a low-cost and sustainable biosorbent to remove Fe3+, Cu2+, Ni2+, Pb2+, and Zn2+ from an AMD and other model solutions with an initial pH of 2.24. Batch adsorption tests were conducted to systematically investigate the influences of initial pH, compost dose, the presence of Fe3+ and SO42− ions, and the pH-induced Fe precipitates on the removal performance. The involved removal mechanisms were explored by conducting stepwise precipitation tests, sequential extraction tests, and Fourier transform infrared spectroscopy (FTIR) characterization. It was found that the addition of the compost removed over 90% of Zn, Ni, Cu, and Pb at pH 5.80, 5.50, 4.50, and 3.00, respectively. At low compost doses, the presence of Fe3+ and SO42− ions hindered the removal since the competition effect of Fe3+ ion and lower absorbability of metal-sulfate complexes, respectively. Sequential extraction tests revealed that higher fractions of Fe, Cu, and Pb were strongly immobilized through complexation and precipitation relative to Ni and Zn. Additionally, the pH-induced Fe precipitates did not favor the removal of the HMs, probably due to the adsorption of organic components released from the compost. This study suggests that compost have the potential to remove HMs from acidic wastewater without pre-neutralization.

New insights into the remediation of chromium-contaminated industrial electroplating wastewater by an innovative nano-modified biochar derived from spent mushroom substrate: Mechanisms, batch study, stability and application

To enhance the adsorption and detoxification capabilities of hexavalent chromium (Cr(VI)) using agricultural spent mushroom substrate (SMS), this study pioneered the preparation of biochar (NBC) from Lentinus edodes spent substrate. Subsequently, nano iron sulfide (FeS) particles were integrated onto NBC with carboxymethyl cellulose (CMC) as a stabilizer, resulting in a novel composite biosorption material, nFeS-BC. The adsorption and reduction potential of both NBC and nFeS-BC against Cr(VI) were evaluated through batch experiments, which identified pH as a critical factor influencing adsorption efficiency. Remarkably, nFeS-BC exhibited a superior maximum adsorption capacity (qmax) of 99.57 mg g−1 and a reduction efficiency of 68.65%, outperforming NBC by 277.73% and 211.76% under optimized conditions, respectively. Characterization techniques including Scanning Electron Microscopy-Energy Dispersive X-Ray (SEM-EDX), Fourier Transform Infrared Spectroscopy (FT-IR), and X-ray Photoelectron Spectroscopy (XPS) elucidated the removal mechanisms, predominantly attributed to ion exchange, electrostatic attraction, functional group interaction, and redox reaction. The carbon-oxygen functional groups and nano particles were crucial in the adsorption and reduction processes. Compared with NBC, the incorporation of FeS particles increased the specific surface area and pore volume of nFeS-BC by 130.86% and 183.77%, respectively. nFeS-BC owned a shelf-life of up to ∼3 months of use and exhibited excellent performance in the processing of actual electroplating wastewater with q of 16.71 mg g−1 under 0.1 g L−1 dosage. These findings underscore the potential of nFeS-BC as an efficient material for Cr(VI) removal, presenting a novel adsorbent for the sustainable detoxification of contaminated water resources and the potential for using agricultural waste materials in environmental remediation.

Chemical magnetic field-assisted batch polishing method of 316L stainless steel

316L stainless steel has been extensively employed in the manufacturing of medical equipment and biomedical implants because of its good ductility, corrosion resistance and biocompatibility, etc. However, there has always been a non-neglected problem of low polishing precision and efficiency in the whole machining chain for such parts, hence, it is difficult to meet the batch demand of the market for 316L stainless steel with high-precision surface. Based on the principle of magnetic field-assisted batch polishing (MABP) proposed by our research team previously, a novel chemical magnetic field-assisted batch polishing (CMABP) method here is developed by adding chemical reagents (i.e., the mixture of oxalic acid and hydrogen peroxide) in the preparation process of regular magnetic brush, desiring and expecting to further realize the polishing of 316L stainless steel with higher precision and efficiency simultaneously. The preliminary experimental results demonstrated that the value of surface roughness Sa after CMABP became smaller and the material removal rate increased comparing to that after MABP, which did verify the potential advantage of the established CMABP approach. In detail, CMABP experiments with pH value and H2O2 concentration as variables were carried out quantitatively. The results suggested that, within the set range of pH value (from 2 to 7) and H2O2 concentration (from 0.3 wt.% to 2.0 wt.%), when pH was chosen as 4 and H2O2 concentration was adjusted as 2.0 wt.%, the value of Sa after CMABP was the minimum, which could be 38% lower than that of MABP approximately. Nonetheless, material removal rate reached to the maximum, which could be around 168% more than that after MABP, when pH and H2O2 concentration were determined as 3.0 and 2.0 wt.%, respectively. Additionally, the discrepancy between the chemical and the regular magnetic brushes were detected and analyzed comparatively both at macro and micro scales. Also, the products on the surface of 316L stainless steel, such as the weak-binding layer and the passive layer, were discovered and taken to interpret the experimental phenomena of the surface roughness and material removal rate varying with the content of chemical reagents in CMABP, thereby revealing the material removal mechanisms correspondingly and interestingly. This work is capable of providing valuable reference undoubtedly for batch precision polishing of 316L stainless steel and other significant functional materials.

Study on ultrasonic-assisted lapping performance and material removal behavior of diamond/SiC composites

Diamond/SiC composites have emerged as a new generation of highly promising materials for semiconductor packaging due to their excellent thermal conductivity. However, the exceptionally hard diamond and SiC phases in the composites have made precision machining a substantial difficulty. This study specifically explores the utilization of ultrasonic-assisted lapping (UAL) to enhance the machining performance of diamond/SiC composites. The focus is on investigating the effects of UAL on the material removals, including the brittle-ductile transition of sample interfacial diamond at different ultrasonic conditions, as well as the surface morphology of diamond/SiC composites. The removal mechanism of diamond/SiC composites under different machining conditions and the transient impact action of the abrasive were systematically analyzed, taking into account the abrasive size, the mechanical effects of ultrasonic vibration, and the interplay of processing parameters. The experimental results reveal that UAL significantly changes the traditional removal mode of diamond/SiC composites. At a constant rotational speed, the diamond abrasive size in the lapping solution exerts the primary influence on the sample surface morphology, followed by the average power of ultrasonic. Compared to conventional lapping methods, UAL improves the removal rate by 10.3 %, 5.4 %, and 5.3 % for abrasive sizes of 8 μm, 4 μm, and 1 μm, respectively. Optimally, the best surface quality finish of diamond/SiC composites was achieved with a lapping solution containing 4 μm abrasive particles and an average ultrasonic vibrator power of 75 W. This study underscores the potential of UAL to enhance the efficiency and quality of diamond/SiC composite machining.

Combined hybrid machining of laser ablation-drilling small holes in Cf/SiC composites

Carbon fiber-reinforced silicon carbide composite material (Cf/SiC) serves as a typical advanced material for fabricating hot-end components of aircraft engines. Its unique properties, including high hardness and anisotropy, pose significant challenges in processing. Nevertheless, a crucial structural element of hot-end components, specifically the cooling and heat dissipation holes, necessitates hole machining within the Cf/SiC composites. The intricate nature of machining this material often leads to compromised surface quality and severe wear on cutting tools during the hole machining process. This study delves into the feasibility of combined hybrid machining of laser ablation-drilling(L-DCM) for fabricating small holes in woven Cf/SiC composites, along with elucidating the underlying material removal mechanisms. The findings reveal approach significantly enhances the cutting performance of hard alloys tools when dealing with ceramic matrix composites. Notably, the wear mechanisms of the cutting tools primarily involve abrasive wear and adhesive wear. The primary processing defects observed in the small holes include fiber pullout at the entrance and exit, as well as material delamination at the exit, which are primarily attributed to debonding at the layer interface and brittle fracture of the matrix. The subsequent drilling process, conducted based on laser drilling, effectively eliminates thermal defects such as the heat-affected zone and recast layer, as well as morphological defects like taper. Additionally, this approach mitigates the tool wear process, minimizes the impact of compression effects on material removal, and enhances the shear action of the tool. Consequently, the layer interface remains securely bonded and intact after processing, thereby preserving the material's strength.

The Molecular Design of a Macrocycle Descaling Agent Based on Azacrown and the Mechanism of Barium Sulfate Scale Removal.

The formation of barium sulfate scale is a persistent and formidable challenge across various industrial processes. In order to effectively mitigate this problem, this study proposed the development of an innovative azacrown ether-based macrocycle descaling agent. Using density functional theory, an in-depth analysis of the surface energy of different barium sulfate crystal facets was carried out, together with a detailed investigation into the adsorption properties of the functional groups on the (001) surface. A further comprehensive investigation was carried out to determine how changes in the nitrogen and oxygen atoms in the crown ether framework influence its adsorption affinity to barium ions. In addition, a detailed analysis was carried out to elucidate the molecular interactions between crown ethers with pyridine carboxylic acid side chains and barium sulfate. The newly developed decalcifying macrocycle descaling agent exhibited superior adsorption performance, achieving an adsorption energy for barium ions approximately -4.1512 ev higher than that of conventional DTPA decalcifiers. This remarkable improvement is mainly attributed to the pivotal role of electrostatic forces in the coordination process between the macrocycle descaling agent and barium ions, with an electrostatic potential value reaching -143.37 kcal/mol. This discovery not only introduces a novel approach to the removal of barium sulfate scale but also highlights the significant potential of macrocycle chemistry in industrial applications.

Removal of Fe2+ in coastal aquaculture source water by manganese ores: Batch experiments and breakthrough curve modeling.

Excessive Fe2+ in coastal aquaculture source water will seriously affect the aquaculture development. This study used manganese sand to investigate the removal potential and mechanism of Fe2+ in coastal aquaculture source water by column experiments. The pseudo-first-order kinetic model could better describe Fe2+ removal process with R2 in the range of 0.9451-0.9911. More than 99.7% of Fe2+ could be removed within 120 min while the removal rate (k) was positively affected by low initial concentration of Fe2+, high temperature, and low pH. Logistic growth (S-shaped growth) model could better fit the concentration variation of Fe2+ in the effluent of the column (R2>0.99). The Fe2 breakthrough curve could be fitted by Bohart-Adams, Yoon-Nelson, and Thomas models (R2>0.95). Smooth slices with irregular shapes existed on the surface of manganese sand after the reaction while Fe content increased significantly on the surface of manganese sand after the column experiment. Moreover, FeO (OH) was mainly formed on the surface of manganese sand after the reaction. PRACTITIONER POINTS: Fe2+ in coastal aquaculture source water could be removed by manganese ores. The pseudo-first-order kinetic model better described the Fe2+ removal process. FeO (OH) was mainly formed on the surface of manganese sand after the reaction.

Study on the removal mechanism of Si3N4 ceramic material in rotary ultrasonic grinding based on multi-abrasive coupling simulation

Study on the removal mechanism of Si3N4 ceramic material in rotary ultrasonic grinding based on multi-abrasive coupling simulation

Optimization and machinability evaluation for WEDM of austempered ductile iron

Abstract Wire electrical discharge machining (Wire EDM) is a non-contact CNC machining that removes material from a workpiece with electrical sparks. Optimization of parameters involved in wire EDM is essential for better operational economics and energy usage. The major goal and objective of this research are to assess the machining parameters, like surface roughness Ra, material removal rate MRR, and hardness HV by experimental investigation utilizing the wire cut EDM machine and austempered ductile iron (ADI) as the work material. An artificial neural network (ANN) has been employed to create a prediction model using experimental data. The Aquila optimization approach is then used to obtain the ideal operating parameters. With Aquila optimization, the predicted optimum values for MRR, Ra, and Hardness are 3.529 mm3/min, 1.966 µm, and 367 HV, respectively, when the input parameters are pulse ton 16 µs, pulse-toff time toff 14 µs, servo voltage 50 V, and current 3 A. Finally, SEM and 3D roughness analysis have been carried out to study surface morphology and material removal mechanism.

Controlling synthesis of defect state lignin-derived carbon and application for U(VI) removal from aqueous solution: Effects of oxygen-defect and grain-size

Lignin has deemed to be the main polluting component of paper industry wastewater. But developing a potential strategy for utilization of lignin is a challenges problem. Lignin derived materials present potential performance for heavy metal wastewater treatment due to their unique physicochemical properties, and were found to be promising candidate materials in U(VI) removal. However, it is still lacking of a comprehensive understanding that the influences of surface oxygen-defect and grain-size on U(VI) removal processes. Here, using lignin as the raw material, combining plasma treatment technology to prepare defect states Lignin Derived Carbon (LDC), and exploring the influences of surface oxygen-defect and grain-size on their removal U(VI) process. The results indicated that with the reducing of LDC particle size (from ∼4 to ∼ 1 μm), the removal performance of U(VI) was improved. And the U(VI) removal performance of LDC was further improved by introducing of oxygen defect via H2 plasma etch. The characterization analysis of defect states LDC before and after reaction with U(VI) shown that the U(VI) removal mechanism was dominated by defects site complexation. These finding provide deep insight into the recycling of industrial solid wastes lignin and improving of U(VI) removal performance via defect controlling technology.

Removal mechanisms of pentachlorophenol in a horizontal-flow anaerobic immobilized biomass reactor (HAIB) inoculated with an indigenous estuarine sediment microbiota: adsorption and biodegradation processes.

Pentachlorophenol (PCP) is a highly toxic and carcinogenic compound with significant environmental impact, necessitating effective treatment technologies. This study evaluates PCP removal mechanisms, including adsorption and biodegradation, during the startup of a horizontal-flow anaerobic immobilized biomass reactor (HAIB), and examines the impact of PCP concentration on microbial diversity using denaturing gradient gel electrophoresis (DGGE). The primary mechanism for PCP removal in the HAIB was adsorption, effectively described by the Freundlich isotherm model. Adsorption efficiency ranged from 86 to 104% for PCP concentrations between 0.2 and 5.0mg/L, and 46% to 64% for concentrations between 0.098 and 0.05mg/L. Additionally, PCP degradation intermediates such as 2,3-DCP and 2,6-DCP were detected, indicating that biodegradation also occurred in the HAIB. Organic matter degradation averaged 81 ± 9%, and methane content in the biogas averaged 46 ± 9%, confirming the anaerobic process. No inhibition of microbial activity was observed due to PCP toxicity, even at a PCP load of 5mg PCP/g STV per day. While the archaeal community showed only slight changes, with similarity coefficients ranging from 88 to 95%, the bacterial community was significantly affected by PCP, with similarity coefficients ranging from 18 to 50%. Bacterial groups were responsible for the initial PCP degradation, while the archaeal community was involved in metabolizing the resulting byproducts. The use of indigenous inoculum from the Santos-São Vicente estuary demonstrated its potential for effective PCP removal. Polyurethane foam proved to be an effective support material, enhancing the adsorption process and reducing PCP toxicity to the microbial consortium. This study provides valuable insights into PCP adsorption and biodegradation mechanisms in HAIB, highlighting the effectiveness of indigenous inoculum and polyurethane foam for PCP removal.

Activation of peroxomonosulfate by manganese-containing non-homogeneous catalysts prepared via a soft template calcination strategy for efficient degradation of carbamazepine

Manganese (Mn)-containing inhomogeneous catalysts have demonstrated potential to activate peroxymonosulfate (PMS), but may be constrained by low efficiency and poor resistance to environmental disturbances. According to the soft template calcination strategy, g-C3N4 with Mn doping was synthesized to improve PMS activation through an effective Mn(II)/Mn(III)/Mn(IV) cycle. The constructed Mn25@CN/PMS system achieved complete and rapid removal of carbamazepine (CBZ) at 0.3 g/L catalyst and 2 mM PMS. Its corresponding rate constant of pseudo-first-order was 0.3424 min−1, and it was 3424 and 16.15 times higher than that of pure g-C3N4/PMS system and CN/PMS system, respectively. More strikingly, the catalysts exhibited excellent resistance to environmental impacts, with CBZ removal rates exceeding 95% under the influence of different anions, cations, aqueous pH values, and humic acid (HA) concentrations. Subsequently, it was proposed a reliable catalytic mechanism for CBZ removal and PMS activation derived from electron paramagnetic resonance (EPR) tests and quenching experiments. The O2·- and 1O2 played a major role in the CBZ removal process. This research provides a perspective soft template strategy for PMS activation using highly efficient catalysts with high resistance to environmental impacts, which provides new ideas to alleviate environmental issues.

Efficient and regenerative phosphate removal from wastewater using stable magnetite/magnesium iron oxide nanocomposites

Using magnetite-based nanocomposite adsorbents to remove and recycle phosphate from wastewater is crucial for controlling eutrophication and ensuring the sustainable use of phosphorus resources. However, the weak structural stability between magnetite and adsorptive nanoparticles often reduces phosphate removal efficiency in real-world applications. This instability primarily results from the loss of adsorptive nanoparticles from the magnetite surfaces, particularly when metal oxide nanoparticles are used for phosphate removal and recycling. In this study, we present a top-down approach that involves lattice locking magnesium iron oxide nanoparticles to the magnetite core, preventing magnesium loss from the magnetite surfaces. These nanocomposites exhibit exceptional performance in both phosphate recycling and removal, with a maximum adsorption capacity of 101.8 mg P·g−1. Excellent adsorption performance is also observed even in the presence of competing anions at phosphate-to-competing ion molar ratios of 1:5, 1:25, and 1:100, as well as dissolved organic matter, across a broad pH range of 4–10. The adsorbent also demonstrated minimal magnesium release during regeneration and in acidic conditions. Microscopic and spectroscopic analyses reveal that surface precipitation is the primary mechanism of phosphate removal in the magnesium-containing shells. The findings of this study address the current limitations of magnetite nanocomposites in phosphate removal, paving the way for the development of highly stable and sustainable nanocomposites for various chemical removal and recycling applications in wastewater treatment.

Efficient Capture of Phosphate From Aqueous Media Using Bimetallic La‐Zr‐MOF

ABSTRACTDeposition of excessive phosphate in natural water column caused several issues, like the eutrophication and destruction of aquatic ecosystems. Adsorption has been an effective and convenient method for phosphate elimination. Herein, a novel bimetallic metal–organic framework adsorbent, namely, La‐Zr‐MOF, was prepared, and the morphology, crystallite, characteristic functional groups, specific surface area, and composite material surfaces were analyzed using XRD, FT‐IR, SEM‐EDS, and BET. The adsorption performance of the adsorbent was systematically evaluated by batch adsorption experiments, and the adsorption thermodynamic and kinetic properties were analyzed. The results reveal that La‐Zr‐MOF exhibits a high selectivity and sorption performance for phosphate, and the adsorption of La‐Zr‐MOF follows the Langmuir and pseudo–second‐order models; the phosphate removal procedure is a chemisorption accompanied by an endothermic reaction, and the maximum capacity was 127.7 mg g−1. Combined with batch adsorption experiments, kinetic and thermodynamic studies and various characterization analyses together revealed the phosphate removal mechanism, mainly ligand exchange and electrostatic interactions.

Theoretical investigation of anisotropic material removal mechanism in robotic belt grinding single crystal superalloy process

Theoretical investigation of anisotropic material removal mechanism in robotic belt grinding single crystal superalloy process