Optimal Experimental Conditions Research Articles

Synthesis, Characterization, and Optimization of Novel Furan-ring Fused Chalcones via Radical Cyclization of α,β-Unsaturated Ketones and Cyclic Ketone

Abstract: Novel Furan-ring Fused Chalcones (FFC) were synthesized using a radical cyclization reaction of α,β-unsaturated ketones with cyclic ketone as the model reaction to attain this goal. In this study, traditional and microwave-assisted methods for the efficient and cost-effective synthesis of furan-ring fused chalcones in mild reaction conditions are compared and optimized. The goal is to develop a reliable and adaptable synthetic technique that may be used to produce these useful chalcone derivatives quickly and effectively. The optimal experimental conditions for these reactions were carefully determined using two independent methodologies: conventional (Method A) and microwave (Method B). The results indicated that the proposed method B could be used effectively in the future to synthesize novel furans with short reaction times and acceptable yields (87-94 %), and products were purified by column chromatography and preparative thin layer chromatography (PTLC). All new compounds were characterized by 1H-NMR, 13C-NMR, LC-MS, and elemental analyses.

EXPERIMENTAL CONDITIONS FOR ROOM TEMPERATURE FERROMAGNETISM IN Fe-DOPED SnO2 VIA MECHANOCHEMICAL MILLING AND THERMAL TREATMENT

Abstract Identifying optimal experimental conditions, preferably through a simple and cost-effective method, for the fabrication of oxide-diluted magnetic semiconductors, such as Fe-doped SnO2, holds great significance in the quest for spintronic materials operating at room temperature (RT). While mechanochemical milling is a well-established technique meeting these requirements, its numerous milling variables necessitate careful consideration of restricted experimental conditions. In this study, we present some experimental mechanochemical milling conditions to prepare impurity-free iron-doped tin dioxide nanoparticles exhibiting a RT ferromagnetic signal. To achieve this, we investigated the effects of milling time, the choice of the starting Sn reactant, and iron concentration on the purity of Sn1-xFexO2 (x=0, 0.03, and 0.05) nanopowders obtained through mechanochemical milling followed by thermal treatment. Characterization through XRD, XANES, and EXAFS at the Fe K-edge, RT Raman spectroscopy, 119Sn and 57Fe Mössbauer spectroscopies, and magnetic measurements was conducted. Among the experimental techniques, micro-Raman spectroscopy proved most effective in detecting the formation of hematite as an impurity phase. Our results indicate that extending the milling time to 12 h, as opposed to 3 h, employing anhydrous SnCl2, instead of SnCl2·2H2O and using the low iron concentration of x = 0.03, results in proper conditions for producing impurity-free samples with a robust RT ferromagnetic signal. The oxidation states for iron and tin ions were determined to be 3+ and 4+, respectively, with both occupying octahedral sites, suggesting iron's replacement of tin. Our findings propose that both the bound magnetic polaron and RKKY models offer potential explanations for the origin of the ferromagnetic signal observed at room temperature in Sn0.97Fe0.03O2 sample milled for 12 h.

Electrochemical Sensor for the Detection and Accurate Early Diagnosis of Ovarian Cancer.

Ovarian cancer (OC) has the highest mortality rate among malignant tumors, primarily because it is difficult to diagnose early. Exosomes, a type of extracellular vesicle rich in parental information, have garnered significant attention in the field of cancer diagnosis and treatment. They play an important regulatory role in the occurrence, development, and metastasis of OC. Consequently, exosomes have emerged as noninvasive biomarkers for early cancer detection. Therefore, identifying cancer-derived exosomes may offer a novel biomarker for the early detection of OC. In this study, we developed a metal-organic frameworks assembled "double hook"-type aptamer electrochemical sensor, which enables accurate early diagnosis of OC. Under optimal experimental conditions, electrochemical impedance spectroscopy technology demonstrated a good linear relationship within the concentration range of 31-3.1 × 106 particles per microliter, with a detection limit as low as 12 particles per microliter. The universal exosome detection platform is constructed, and this platform can not only differentiate between high-grade serous ovarian cancer (HGSOC) patients and healthy individuals but also distinguish between HGSOC patients and nonhigh-grade serous OC (non-HGSOC). Consequently, it provides a novel strategy for the early diagnosis of OC and holds great significance in clinical differential diagnosis.

Laboratory study on the transformation of oil-water interface properties under direct current electric field

Interface tension is one of the important mechanisms that affect crude oil recovery and plays an important role in the development of tight oil reservoirs. Electrical-enhanced oil recovery can be used as a technology to reduce interfacial tension and improve crude oil recovery. In the previous research process of Electrical-enhanced oil recovery, the focus was more on the influence of electric field on wettability, and the understanding of the changes in interfacial tension under electric field action is not yet comprehensive. This article designs an orthogonal experiment to study the effect of electric field on oil-water properties. The degree of influence of three factors, namely sodium chloride solution concentration (C), direct current voltage (V), and voltage action time (t), on interfacial tension is studied. Gas chromatography, four component analysis, and Fourier transform infrared spectroscopy are combined to discuss the mechanism of the influence of changes in solution pH, crude oil components, and oil phase functional groups on interfacial tension. The results show that an external electric field can effectively reduce the interfacial tension between oil and water, and the maximum change in interfacial tension after the experiment can be reduced from 23.21 mN/m to 0.37 mN/m; Through range analysis, it can be concluded that the concentration of sodium chloride solution has the greatest impact on interfacial tension, followed by DC voltage and voltage action time. The optimal experimental conditions are 0.5mol/L sodium chloride solution, 10V DC voltage, and a voltage action time of 18 hours, and the change in interfacial tension is related to the increase in pH value. The change in crude oil composition is also an important reason for the decrease in interfacial tension under external electric fields. Finally, Fourier transform infrared spectroscopy was used to determine that under the action of an electric field, the increase in pH of the sodium chloride solution resulted in the formation of carboxylate salts through chemical reactions between alkaline substances of solution and acidic substances of the oil, which were the key factors in reducing interfacial tension. This study helps to understand and explore the principles and mechanisms of Electrical-enhanced oil recovery in improving oil recovery, with the aim of contributing to the development and promotion of Electrical-enhanced oil recovery technology.

Optimization and production of dairy-cereal grain-based probiotic beverage powder and its probiotic survivability under simulated gastric and pancreatic conditions

The present study uses maize flour and skimmed milk powder to develop a probiotic dairy-cereal-based food powder by spray drying and using response surface methodology for optimization. The processing parameters and ingredients, including inlet spray drying temperature (140–170 ℃), maize flour (80–120 g), and skim milk powder (60–80 g), were optimized against probiotic survivability count, moisture, sensory score, bulk density, and wettability as responses using response surface methodology. The optimum experimental conditions obtained to manufacture acceptable-quality powder were an inlet temperature of 151 ℃, an amount of maize flour of 102.74 g, and skim milk powder at 69.88 g. The probiotic survivability (8.35 log CFU/g) was observed at more than the recommended level (6.0 log CFU/g) due to the probiotic strain's microencapsulation by skim milk and maize flour components. The optimized powder had good nutritional and functional values and was observed to have acceptable water activity, surface structure, and color values. The shelf life of the product on the basis of probiotic survival (minimum 6.0 log CFU/g) was found to be 49 days at 4 ℃. Gastric and pancreatic survival was also observed at more than 50% in refrigerated conditions for up to 56 days of storage.

An antifouling electrochemical aptasensor based on a Y-shaped peptide for tetracycline detection in milk

Nonspecific adsorption of non-target components (especially proteins) in food matrix on sensing surfaces deteriorates accuracy and sensitivity of electrochemical sensors, which is a key challenge for food safety sensing. Therefore, electrochemical sensors with antifouling capability of high-protein food matrices are highly desired. In this paper, an efficient and simple antifouling electrochemical aptasensor for tetracycline (TC) analysis was constructed based on a self-designed Y-shaped peptide [CPPPPEK-(RSERSERSE)2] consisting of cysteine as the anchoring segment, polyproline as the supporting segment, and -EK-(RSERSERSE)2 as antifouling branches. Hydrophilic and electrically neutral amino acid sequence and Y-shaped space structure of the peptide endow the sensing surface with good antifouling performance in protein solutions and diluted milk. Under optimized experiment conditions, the proposed aptasensor can detect TC with a wide linear range (0.01–100 ng mL−1) and a limit of detection of 5.3 pg mL−1 (S/N = 3). The spiked recovery experiments confirmed high accuracy of the aptasensor in diluted milk without other pretreatments (recoveries: 90.96%–95.86%). This strategy offers a valid way to reduce matrix interference, showing a promise to be extended to other sensing systems for different targets.

Thymine-Hg2+-Thymine strategy in MOF-based electrochemical aptamer sensor for PAEs detection

Phthalate acid esters (PAEs), known food contaminants, can lead to reproductive problems, respiratory diseases, childhood obesity, and neuropsychological disorders. This work aims to develop an electrochemical aptamer sensor for the detection of DAP and its analogs. To achieve specific recognition ability for PAEs, we have introduced the thymidine-Hg2+-thymidine strategy for the first time in an electrochemical aptamer sensor, incorporating metal–organic frameworks (MOFs) as the carrier for the aptamer. Additionally, nano signal amplification technology was applied by immobilizing MXene on the electrode to intensify the sensor’s current signal. In the presence of PAEs, these molecules specifically bound to the aptamers, resulting in competitive release of Hg2+ and aptamers connected to Hg2+, subsequently reducing current signaling. Under optimal experimental conditions, the designed sensor achieved a linear range from 1.65 × 10−5 mg/mL to 3 × 10−3 mg/mL and an extremely low detection limit of 8.94 × 10−6 mg/mL. Furthermore, it exhibited good reliability and practicality in detecting actual samples.

Hydrophobic deep eutectic solvent-based vortex-assisted dispersive liquid–liquid microextraction with UV–visible spectrophotometry for copper determination in waste printed circuit boards

ABSTRACT Nearly all electronic devices utilise Printed Circuit Boards (PCBs), which contribute significantly to the generation of electronic waste (e-waste). They are rich in metal content, with copper being present in higher percentages. In this work, a simple, efficient and environment-friendly pre-concentration technique was developed, using hydrophobic deep eutectic solvent as an extractant in vortex-assisted dispersive liquid–liquid microextraction. This pre-concentration technique is coupled with spectrophotometry for the determination of copper in PCBs. The complexing agent, sodium diethyl di-thiocarbamate (DDTC), and copper formed a complex in the 2–3 pH range. The Cu-DDTC complex was vortexed for 1 min at 2800 rpm to extract in hydrophobic DES. The sediment was analysed using a UV–Visible spectrophotometer at λ max 435 nm. The optimisation parameters, including pH, extraction solvent selection and its volume, concentration and volume of chelating agent, interference of forein ios, etc., have been assessed. Analytical figures of merit such as limit of detection (1.98 μg/L), limit of quantification (5.9 μg/L), relative standard deviation (3.4%) and enrichment factor (10) have been obtained under optimal experimental conditions. The method was validated by a certified copper solution and applied successfully to determine copper in waste PCBs of personal computers.

Highly sensitive rhodamine B dye-based electrochemical sensor for lactose detection

Lactose (LAC) is the main disaccharide sugar found in milk and dairy products, making it easily accessible as a food source. In addition to its importance for human and animal health, LAC concentrations serve as a biomarker of milk quality. In this study, we reported the detection of LAC using a highly sensitive electrochemical sensor based on rhodamine B (RhB) dye. The prepared RhB-based sensor exhibited excellent characteristics, including a straightforward manufacturing technique, cost-effectiveness, and exceptional sensitivity. We conducted a comparative analysis of the electrochemical response of the novel RhB-based sensor, evaluating its electrochemical performance across varying LAC concentrations and when different analyte materials (glucose, fructose, and maltose) were employed. The proposed analytical method was utilized to determine LAC using an electrochemical RhB-based sensor under optimal experimental conditions. As a result, it was experimentally observed that high sensor sensitivity of RhB based sensor against LAC was inversely proportional to the impedance value and directly proportional to conductance which corolated with the transport mechanism of RhB.

Simulation and Experimental Study of Circulatory Flash Evaporation System for High-Salt Wastewater Treatment

Treatment methods for high-salt wastewater mainly consist of physical methods, chemical methods and biological methods. However, there are some problems, such as slow treatment speed, high investment costs and low treatment efficiency. To address NaCl solutions, in this study, a circulatory flash system was designed based on gas–liquid equilibrium, mass conservation equation and energy conservation equation. A circulatory flash evaporation simulation and a static flash evaporation experiment were conducted on NaCl solutions under various operating conditions to investigate the effects of heating temperature, flash pressure and initial NaCl concentration on the circulatory flash evaporation system. The significance of each factor’s influence on the evaporation fraction and energy consumption was examined through static flash experiments. The simulation results demonstrated that increasing the heating temperature, decreasing the flash pressure and having a higher initial NaCl concentration could enhance the treatment capacity of high-salt wastewater. The flow rate of vapor outlets increased with higher heating temperature but decreased as the flash pressure rose. The experimental results demonstrated that flash evaporation pressure was the primary factor influencing both the evaporation fraction and the energy consumption per unit mass of vapor produced. It was observed that with an increase in heating temperature, the flash pressure decreased and there was a corresponding decrease in energy consumption per unit mass of vapor produced. The optimal experimental conditions were achieved at a heating temperature of 99 °C, a flash pressure of 15 kPa, and an initial NaCl concentration of 20%.

Thiol-based chemically modified carbon screen-printed electrode for simultaneous quantification of trace level Pb(II) and Cd(II).

Present work reports, the development of a novel electrochemical sensor based on a diazonium-coupling reaction and covalent attachment of the -NH2 group of cysteamine (Cyst) on screen-printed carbon electrode (SPCE), for simultaneous determination of Pb(II) and Cd(II). Initially, the in-situ generated 4-carboxyphenyl (4-CP) diazonium salt was electro-grafted to generate 4-CP/SPCE, followed by covalent bonding of terminal carboxylic group of 4-CP with -NH2 group of Cyst to give Cyst/4-CP/SPCE. The modified electrode showed an enhanced selectivity and sensitivity toward the quantification of Pb(II) and Cd(II) using square wave anodic stripping voltammetry (SWASV) without mutual interference. Under optimal experimental conditions, the newly designed sensor showed a wide linear range of 0.01µM to 0.7µM. The limit of detection (LOD) obtained was 0.882nM (0.09 ppb) and 0.65nM (0.134ppb) for Cd(II) and Pb(II), respectively. The modified SPCE exhibited good stability, selectivity, and reproducibility. Furthermore, the sensor was successfully applied for the determination of Pb(II) and Cd(II) ions in water samples which illustrated excellent recoveries in different spiked samples and the results were in line with the standard ICP-AES analysis.

The heat dissipation by the multi-needle electrode structure ionic wind generator

Ionic wind generated by atmospheric pressure discharge can be used for propulsion, heat dissipation, food drying, which shows the unique advantages of no mechanical parts and fast response. However, the wind speed and the energy efficiency of ionic wind generator are very low, which limit its application. In this paper, an ionic wind generator, constructed with needle-net electrode structure and powered by high-voltage positive dielectric current (DC) power supply, is built for cooling of a metal oxide semiconductor field effect transistor (MOSFET). The energy efficiency and wind speed of the ionic wind generator are optimized by adjusting the electrode structure and applied voltage amplitude. The results show that when the discharge spacing is fixed at 10 mm and the optimal needle spacing is 17.5 mm with 6 needles at 14 kV, the ionic wind velocity can reach a maximum value 3.20 m s−1 and the energy efficiency is 1.90%. Under optimal experimental conditions, the heat dissipation performance of MOSFET is significantly enhanced compared to using only a heat sink. With cooling by the ionic wind generator, the MOSFET junction temperature can be lowered by about 29 °C after 240 s operation.

The Elimination of Levofloxacin from High-Salinity Wastewater via the Electrochlorination Process

The electrochlorination (E-Cl) process has attracted much attention as it is a highly efficient method for treating organic compounds in hypersaline wastewater. In this study, the E-Cl process was utilized for the removal of antibiotics. The optimal experimental conditions were determined to be a NaCl concentration of 100 mM, a current density of 1.5 mA/cm2, a pH of 7.0, and a plate spacing of 1 cm, with a levofloxacin (LEV) degradation efficiency reaching as high as 99% using this setup. The effects of the presence of other ions and humic acid on the E-Cl process were investigated, and it was found that the degradation of LEV was not significantly affected by the presence of coexisting substances. In addition, free chlorine was identified as the primary active species for the degradation of LEV by means of a quenching experiment. It was demonstrated by 3D EEM and TOC that LEV was not completely mineralized and that intermediate products may be present. In order to reveal the degradation pathways of LEV, its degradation products were also analyzed via LC-MS, and some possible pathways of LEV degradation in this system were proposed. The successful degradation of LEV demonstrated that the E-Cl process is an efficient and promising technique for the treatment of organic pollutants in high-salinity wastewater.

Exploring the structural characteristics and dye removal capabilities of powder-, granule- and film- shaped magnetic activated carbon derived from Oleaster seed.

Dye pollution in water caused by excessive discharge of industrial effluent has become a major environmental problem in recent decades because of its irreversible effects on human health. In this study, low-cost carbon-based adsorbents synthesized from Oleaster seed (OS) were prepared in three forms of powder (PAC), film (FAC), and granule (GAC) and used for the removal of methylene blue dye. The properties of the synthesized adsorbents were characterized by SEM-EDX, BET, XPS and FTIR analyses. The maximum adsorption capacity (qmax) of PAC, FAC, and GAC adsorbents were obtained as 68.49, 32.25, and 15.10 mg/g, respectively at the optimum experimental conditions of pH = 10, adsorbent dosages of 0.5, 1, and 2 g/l, contact times of 60, 90, and 120 min, dye concentration of 10 mg/L, and temperature of 25°C. The Langmuir isotherm well described the equilibrium data for all three adsorbents. The pseudo-second-order kinetic model provided the best fit with the adsorption data obtained from all three adsorbents. Adsorption occurred spontaneously through a combination of chemical and physical mechanisms, with a thermodynamically exothermic process. The desorption experiments demonstrated that all the adsorbents have substantial potential for recovery. The novel activated carbon/alginate composite films are proposed as more promising biosorbents to remove MB dye from the aquatic environment compared to GAC adsorbents.

Salt slag and rice husk ash as raw materials in zeolite synthesis: Process optimization using central composite rotational design

The growing demand of zeolites for many industrial applications has led to a search for eco-friendly alternatives for their production, in an attempt to reduce costs, save natural resources and alleviate the associated environmental impacts. In the present study, hazardous aluminum salt slag (aluminum source) and rice husk ash (silicon source) were used as secondary raw materials to synthesize sustainable NaP-type zeolites through a hydrothermal process. A central composite rotational experimental design was applied to evaluate the effect of the reaction time and hydrothermal temperature on the obtained zeolites crystallinity. Using the proposed experimental design, temperatures between 85 and 115 °C and different reaction times (2–28 h) were tested. It was found that the interaction between the variables (time and temperature) and both variables, independently, exerted a significant influence on the crystallinity of the zeolites. The optimal experimental conditions (105 °C and 20 h), statistically determined, enabled a high degree of crystallinity (>73%) to be achieved. Thus, the use of hazardous aluminum and agri-food wastes as unconventional precursors for the production of zeolites represents a sustainable alternative to manage these wastes, by transforming them into secondary raw materials.

Effects Analysis of FAME on the Engine Characteristics of Different Polymerized Biofuels in Compression Ignition Engine

Environmental pollution caused by marine engines fueled with fossil fuels is a matter of growing significance. The search for renewable and clean energy sources and improvements in the way fossil fuels are burnt aims to reduce the environmental impact of these engines. For this purpose, fatty acid methyl esters were produced from pure canola oil using KOH-assisted methanol-based transesterification with a maximum yield of 90.68 ± 1.6%. The marine engine’s model was created with CONVERGE software, followed by experimental verification. This paper examines the blended fuel characteristics of a diesel engine with biodiesel blends (0%, 5%, 10%, and 15%) at different loads of engines (50%, 75%, and 100%). It also explores the variation in these characteristics of B10 (10% biodiesel–diesel blends) at three different load conditions and four different EGR rates (0%, 5%, 10%, and 15%). The results indicate that the addition of biodiesel to diesel fuel reduces CO, HC, and soot emissions, while increasing NOx emissions. Additionally, the EGR rate decreases NOx emissions but results in higher levels of soot, CO, and HC emissions. Finally, response surface methodology was used to elicit the engine’s characteristics. It was determined that the optimum experimental operating conditions were 100% engine load, 6.9% biodiesel addition, and 7.7% EGR. The corresponding BTE, BSFC, NOx, and HC emissions were 38.15%, 282.62 g/(kW-h), 274.38 ppm, and 410.37 ppm, respectively.

A homogeneous electrochemiluminescence immunoassay platform based on carbon quantum dots and magnetic beads enrichment for detection of thyroglobulin in serum

Considering the high probability of recurrence or metastasis after thyroidectomy, it is meaningful to develop a rapid, sensitive and specific method for monitoring thyrophyma-related biomarkers. In this study, a homogeneous electrochemiluminescence immunoassay (HO-ECLIA) coupled with magnetic beads (MBs)-based enrichment tactic was established for the determination of thyrophyma-related thyroglobulin (Tg). Importantly, owing to the abundant surface groups and good biocompatibility of carbon quantum dots (CQDs), the incorporation of CQDs onto the Tg antigen surface was achieved, resulting in the formation of Tg-encapsulated CQDs (CQDs-Tg), which served not only as an ECL probe but as a biorecognition element. Under optimal experimental conditions, the proposed platform demonstrated a wide linear range from 0.01 to 100 ng·mL−1 with a detection limit of 6.9 pg·mL−1 (S/N = 3), and performed well in real serum sample analysis against interference. Collectively, the proposed platform exhibited the rapid response, satisfactory sensitivity and specificity toward Tg in complex serum milieu, and held a considerable potential for clinical prognosis monitoring of thyrophyma.

MOF-derived porous carbon microspheres Ni@C-acid as solid-phase microextraction coating for extraction of polycyclic aromatic hydrocarbons from tea infusions

The improvement of the stability and adsorption properties of materials on targets in sample pre-treatment has long been an objective. Extensive efforts have been made to achieve this goal. In this work, metal-organic framework Ni-MOF precursors were first synthesized by solvothermal method using polyvinylpyrrolidone (PVP) as an ideal templating agent, stabiliser and nanoparticle dispersant. After carbonization and acid washing, the nanoporous carbon microspheres material (Ni@C-acid) was obtained. Compared with the material without acid treatment (Ni@C), the specific surface area, pore volume, adsorption performance of Ni@C-acid were increased. Thanks to its excellent characteristics (high stability, abundant benzene rings), Ni@C-acid was used as fiber coatings in headspace solid-phase microextraction (HS-SPME) technology for extraction and preconcentration of polycyclic aromatic hydrocarbons (PAHs) prior to gas chromatography-flame ionization detector (GC-FID) analysis. The experimental parameters of extraction temperature, extraction time, agitation speed, desorption temperature, desorption time and sodium chloride (NaCl) concentration were studied. Under optimal experimental conditions, the wide linear range (0.01-30 ng mL−1), the good correlation coefficient (0.9916-0.9984), the low detection limit (0.003-0.011 ng mL−1), and the high enrichment factor (5273-13793) were obtained. The established method was successfully used for the detection of trace PAHs in actual tea infusions samples and satisfied recoveries ranging from 80.94-118.62 % were achieved. The present work provides a simple method for the preparation of highly stable and adsorbable porous carbon microsphere materials with potential applications in the extraction of environmental pollutants.

Synthesis of Magnetic Attapulgite Nanoparticles Via a Novel Surface Covalent Reaction Method and its Application in the Magnetic Solid Phase Extraction.

In this study, the attapulgite nanoparticle was immobilized on the surface of magnetic nanoparticle Fe3O4 via a novel surface covalent reaction method for the magnetic solid phase extraction (MSPE) for the first time. The surface covalent reaction method has the advantages of controllable steps, and can make the magnetic attapulgite nanoparticle (MANP) have good homogeneity and high stability. Field emission scanning electron microscopy, equipped with an energy dispersive spectrometer, Nitrogen adsorption BET, X-ray diffraction and Fourier transform infrared spectroscopy were applied to characterize the prepared MANP, confirming that the attapulgite nanoparticle could be effectively immobilized on the surface of magnetic nanoparticle Fe3O4 via covalent reactions. Under optimal conditions of the MSPE experiment based on the MANP, the limits of detection were found to be 10ng/mL for melamine and 3ng/mL for cyromazine with a relative standard deviation < 10% by a high-performance liquid chromatography system. Meanwhile, 0.1mg/mL melamine in milk and 0.1mg/mL cyromazine in cucumber can also be detected according to our MSPE procedure. More importantly, the MANP still has good magnetism and enrichment efficiency after several decades of use. These results showed that the MANP prepared by our method is a kind of promising material for the MSPE.

Synthesis and application of dual-functional sorbent SBA-15-Fe3O4-PDA-ODA for removing both water soluble and insoluble pollutants

In this study, inorganic-organic hybrid sorbent SBA-15-Fe3O4-PDA-ODA with functional groups having affinity for both water-soluble and insoluble pollutants was synthesized for treatment of wastewater where Malachite Green (MG) dye and motor oil coexist. In order to enhance the specific interactions between the sorbent and dye via functional groups of polydopamine (PDA), Fe3O4 nanoparticles were encapsulated with SBA-15 and surface functionalization with PDA was accomplished and then the surface of Fe3O4-SBA-15-PDA was modified with octadecylamine (ODA) to remove the oil present in the same environment with dye. While the SBA-15-Fe3O4-PDA-ODA directed to the aqueous phase by magnet provided MG removal thanks to the hydrophilic groups of PDA, it provided motor oil removal thanks to hydrophobicity of ODA when directed to the oil phase. 99.20 % dye removal and 9.24 g/g oil adsorption capacity were achieved from the environment where oil and dye were present together. Besides, the adsorption of MG on Fe3O4-SBA-15-PDA was searched at various pH, dye concentration, adsorbent dosage, and temperature in order to propose optimum experimental conditions for removal of dye and maximum adsorption capacity was determined as 95.83 mg g−1 at optimum conditions (10 mg adsorbent, 10 mg L−1 MG concentration, pH 9). Interaction mechanism between dye and Fe3O4-SBA-15-PDA was explained by studying the adsorption behavior of sorbent derived from the isotherm and kinetic results. The sorbents were characterized by FT-IR, XRD, SEM, N2-adsorption/desorption, water-contact-angle, and VSM measurements. SBA-15-Fe3O4-PDA-ODA sorbent was tested for three successive adsorption cycles for both dye and oil and eventuated insignificant loss in activity when they were recycled. Easy and low-cost fabrication protocol, controllable removal ability of dye and oil will facilitate its versatility in environmental cleanup process for water soluble and insoluble pollutants.