Sustained drug release behavior of captopril-incorporated chitosan/carboxymethyl cellulose biomaterials for antihypertensive therapy.

Captopril (CTP) is an oral drug widely used to treat high blood pressure and congestive heart failure. In this study, CTP-incorporated biomaterials for antihypertensive therapy were synthesized from chitosan, carboxymethyl cellulose, and plasticizers. The physicochemical properties of the prepared biomaterials were characterized using FE-SEM, FT-IR analysis, and physical properties. CTP release experiments were carried out in buffer solutions at various pH values and temperatures. Results indicated that above 99.0 % of CTP was released within 180 min. Optimization of the experimental conditions for CTP release was analyzed by using response surface methodology (RSM). Results of CTP release through artificial skin indicated that CTP was continuously released above 95.0 % from the prepared biomaterials for 36.0 h. The CTP release mechanisms into a buffer and through artificial skin followed pseudo-Fickian diffusion mechanism and non-Fickian diffusion mechanisms, respectively. Moreover, angiotensin-converting enzyme (ACE) inhibition (related to cardiovascular disease) via the released CTP clearly reveals that the prepared biomaterials have a high potential as a transdermal drug delivery agent in antihypertensive therapy.

The Water Quality Management for Recirculating Aquaculture System by Applying Nano Adsorption Technology.

In a fish farm, the water quality is important to ensure fish growth and farm productivity. However, the study of the quality of water using in aquaculture has been ignored until now. Although there are several methods to treat water, nanomaterials have not yet been applied for indoor fish farming because it may difficult to supply a sufficient amount of water, and the operating parameters have not been developed for recirculating aquaculture systems. Nanotechnology can be applied to treat water, specifically through adsorption and filtration, to produce drinking water from surface water and to treat wastewater by processing a high volume of effluent. The adsorption and filtration of seawater has also progressed to allow for desalination of seawater, and this is recognized as a necessary tool for extended treatment protocols of various types of seawater. This study investigated the treatment of aquaculture water using nano-porous adsorbents (e.g., pumice stone) to control the contaminants in seawater in order to maintain the water quality required for aquaculture. The results are used to derive an analytical relationship between the ionic species in aquaculture water, and this provides empirical parameters for a batch reactor for aquaculture. The quality of the influent and effluent for aquaculture is compared using time-series analyses to evaluate the reduction rate of ionic components and thus suggest the optimum condition for fish farming using bioreactor processes.

Ti3C2Tx MXene-Based Three-Dimensional Architecture for Carbon Dioxide Capture.

Dramatic increases in fossil fuel consumption inevitably led to the emission of huge amounts of CO2 gas, causing abnormalities in the climate system. Despite continuous efforts to resolve global atmospheric problems through CO2 capture and separation, success has been limited by poor CO2 selectivity in the CO2/N2 mixture. Herein, we demonstrate the fabrication of a three-dimensional (3D) nanostructure from two-dimensional transition metal carbides (Ti3C2Tx, MXene), and assess its utility as an adsorbent in a CO2 capture system. Through structural and textural analysis, we confirm that the as-prepared MXene possesses high size uniformity with a thickness of ~2.5 nm, and that an MXene aerogel interconnected by MXene nanosheets has a 3D porous architecture with micro/nano porosity (Barrett-Joyner-Halenda (BJH) pore size = 11.4 nm). Moreover, the MXene aerogel exhibits favorable adsorption behavior for CO2, due to the high-quality MXene nanosheets even with a low specific surface area. Our approach could lead to significant advances in CO2 capture by adsorbents and open up new opportunities for mass production.

Recovering Nutrients from Waste Black Water Through Multi-Functional Mesoporous Silica.

In order to prevent the harmful effects in water phase such as eutrophication, industrial and urban sewages must be treated before discharging into the aquatic environment. In this work, amine grafted magnetic nanoporous silica materials are synthesized and applied as an adsorbent for the recovery of nutrients from waste black water. The magnetic force could separate the surface func-tionalized nanoporous silica materials from aqueous medium after treatment, and showed the higher adsorption capacity of nutrients than that of the original mesoporous silica. The multi-functional nanoporous silica adsorbents were effectively removed phosphate and nitrate at 20 °C with the maximum adsorption capacities of 42.5 and 34.9 mg/g, respectively. The overall results indicated that the synthesized multi-functional nanoporous silica sorbents can be a candidate material for the nutrient recovery in wastewater treatment system.

Preparation of Mesoporous Gamma Alumina Derived from Waste Can for Nutrient Recovery Process.

Mesoporous gamma alumina (MGA) was synthesized using aluminum trash containers by a low temperature hydrothermal method for effectively removing phosphate from wastewater. The effects of precursor concentrations in gel precipitation process over the pore size and surface area of MGA were investigated in detail. The phosphate removal by prepared MGAs were rigorously investigated through adsorption isotherms and kinetics of phosphate.

Radio-Frequency Thermal Plasma Treated Activated Carbon Impregnated with Mn and Ag for Volatile Organic Compounds Adsorption.

In this study, we have prepared a composite adsorbent with highly dispersed Mn and Ag nanocatalyst on the surface of activated carbon (AC) by applying the Radio-Frequency (RF) thermal plasma technique for the efficient removal of VOCs. The ACs before and after metal impregnation with RF plasma treatment were characterized by SEM, TEM, EDS, and nitrogen adsorption analysis. Adsorption behaviors of toluene, acetaldehyde, and formaldehyde on ACs before and after modification were also investigated in fixed-bed systems. The experimental adsorption results for VOCs on parent ACs and metal impregnated ACs (Mn-AC and Mn/Ag-AC) were well explained by modified continuous sigmoidal (MCS) model.

Fabrication of granular activated carbons derived from spent coffee grounds by entrapment in calcium alginate beads for adsorption of acid orange 7 and methylene blue.

Biomass-based granular activated carbon was successfully prepared by entrapping activated carbon powder derived from spent coffee grounds into calcium-alginate beads (SCG-GAC) for the removal of acid orange 7 (AO7) and methylene blue (MB) from aqueous media. The dye adsorption process is highly pH-dependent and essentially independent of ionic effects. The adsorption kinetics was satisfactorily described by the pore diffusion model, which revealed that pore diffusion was the rate-limiting step during the adsorption process. The equilibrium isotherm and isosteric heat of adsorption indicate that SCG-GAC possesses an energetically heterogeneous surface and operates via endothermic process in nature. The maximum adsorption capacities of SCG-GAC for AO7 (pH 3.0) and MB (pH 11.0) adsorption were found to be 665.9 and 986.8mg/g at 30°C, respectively. Lastly, regeneration tests further confirmed that SCG-GAC has promising potential in its reusability, showing removal efficiency of more than 80% even after seven consecutive cycles.

Comprehensive reuse of drinking water treatment residuals in coagulation and adsorption processes.

While drinking water treatment residuals (DWTRs) inevitably lead to serious problems due to their huge amount of generation and limitation of landfill sites, their unique properties of containing Al or Fe contents make it possible to reuse them as a beneficial material for coagulant recovery and adsorbent. Hence, in the present study, to comprehensively handle and recycle DWTRs, coagulant recovery from DWTRs and reuse of coagulant recovered residuals (CRs) were investigated. In the first step, coagulant recovery from DWTRs was conducted using response surface methodology (RSM) for statistical optimization of independent variables (pH, solid content, and reaction time) on response variable (Al recovery). As a result, a highly acceptable Al recovery of 97.5 ± 0.4% was recorded, which corresponds to 99.5% of the predicted Al recovery. Comparison study of recovered and commercial coagulant from textile wastewater treatment indicated that recovered coagulant has reasonable potential for use in wastewater treatment, in which the performance efficiencies were 68.5 ± 2.1% COD, 97.2 ± 1.9% turbidity, and 64.3 ± 1.0% color removals at 50 mg Al/L. Subsequently, in a similar manner, RSM was also applied to optimize coagulation conditions (Al dosage, initial pH, and reaction time) for the maximization of real cotton textile wastewater treatment in terms of COD, turbidity, and color removal. Overall performance revealed that the initial pH had a remarkable effect on the removal performance compared to the effects of other independent variables. This is mainly due to the transformation of metal species form with increasing or decreasing pH conditions. Finally, a feasibility test of CRs as adsorbent for phosphate adsorption from aqueous solution was conducted. Adsorption equilibrium of phosphate at different temperatures (10-30 °C) and initial levels of pH (3-11) indicated that the main mechanisms of phosphate adsorption onto CRs are endothermic and chemical precipitation; the surfaces are energetically heterogeneous for adsorbing phosphate.

Efficient recovery of nitrate and phosphate from wastewater by an amine-grafted adsorbent for cyanobacterial biomass production.

Various types of wastewater have been widely utilized in microalgae and cyanobacteria cultivation for environmental and economic reasons. However, the problems of low cell growth and biomass contamination due to direct use of wastewater remain unresolved. In the present study, nitrate and phosphate were separated from wastewater by adsorption and subsequently used for cyanobacterial biomass production. To this end, an amine-grafted magnetic absorbent was synthesized. The synthesized absorbent recovered ca. 78% nitrate and 93% phosphate from wastewater. Regenerated medium was prepared using recovered nutrients as nitrogen and phosphate sources, which were efficiently assimilated by cyanobacterial culture. Compared to synthetic medium, there was no difference in growth and nutrient removal using regenerated medium. The proposed indirect method of wastewater utilization would prevent contamination of the produced biomass by unfavorable substances, which will broaden its potential applications.

Phosphate adsorption ability of biochar/Mg-Al assembled nanocomposites prepared by aluminum-electrode based electro-assisted modification method with MgCl2 as electrolyte.

In this work, the textural properties and phosphate adsorption capability of modified-biochar containing Mg-Al assembled nanocomposites prepared by an effective electro-assisted modification method with MgCl2 as an electrolyte have been determined. Structure and chemical analyses of the modified-biochar showed that nano-sized stonelike or flowerlike Mg-Al assembled composites, MgO, spinel MgAl2O4, AlOOH, and Al2O3, were densely grown and uniformly dispersed on the biochar surface. The adsorption isotherm and kinetics data suggested that the biochar/Mg-Al assembled nanocomposites have an energetically heterogeneous surface and that phosphate adsorption could be controlled by multiple processes. The maximum phosphate adsorption capacity was as high as 887 mg g(-1), as fitted by the Langmuir-Freundlich model, and is the highest value ever reported. It was concluded that this novel electro-assisted modification is a very attractive method and the biochar/Mg-Al assembled nanocomposites provide an excellent adsorbent that can effectively remove phosphate from aqueous solutions.

A novel approach for preparation of modified-biochar derived from marine macroalgae: Dual purpose electro-modification for improvement of surface area and metal impregnation.

In the present study, an aluminum electrode-based electrochemical process was newly adopted as a modification method for fabricating physically and chemically modified biochar derived from marine macroalgae. Specifically, a current density of 93.96 mA cm(-2) was applied for 5 min at pH 3.0. Subsequently, the mixture was stirred continuously for 30 min without electric field, and the dried sample was then pyrolyzed at 450 °C under a N2 environment for 2 h. SEM-EDS and XRD analyses clearly indicated that nano-sized aluminum crystals (beohemite, AlOOH) were uniformly present on the EM-biochar surface. Adsorption equilibrium tests showed that the phosphate adsorption onto EM-biochar agreed well with the Langmuir-Freundlich adsorption isotherm model, with a maximum adsorption capacity of 31.28 mg-P g(-1). These findings suggest that this novel and simple electro-modification method is a reasonable and effective option for simultaneously upgrading both the surface area and chemical properties of biochar.

Lead and copper removal from aqueous solutions using carbon foam derived from phenol resin.

Phenolic resin-based carbon foam was prepared as an adsorbent for removing heavy metals from aqueous solutions. The surface of the produced carbon foam had a well-developed open cell structure and the specific surface area according to the BET model was 458.59m(2)g(-1). Batch experiments showed that removal ratio increased in the order of copper (19.83%), zinc (34.35%), cadmium (59.82%), and lead (73.99%) in mixed solutions with the same initial concentration (50mgL(-1)). The results indicated that the Sips isotherm model was the most suitable for describing the experimental data of lead and copper. The maximum adsorption capacity of lead and copper determined to Sips model were 491mgg(-1) and 247mgg(-1). The obtained pore diffusion coefficients for lead and copper were found to be 1.02×10(-6) and 2.42×10(-7)m(2)s(-1), respectively. Post-sorption characteristics indicated that surface precipitation was the primary mechanism of lead and copper removal by the carbon foam, while the functional groups on the surface of the foam did not affect metal adsorption.

Decolorization of Acid Orange 7 by an electric field-assisted modified orifice plate hydrodynamic cavitation system: Optimization of operational parameters.

In this study, the decolorization of Acid Orange 7 (AO-7) with intensified performance was obtained using hydrodynamic cavitation (HC) combined with an electric field (graphite electrodes). As a preliminary step, various HC systems were compared in terms of decolorization, and, among them, the electric field-assisted modified orifice plate HC (EFM-HC) system exhibited perfect decolorization performance within 40 min of reaction time. Interestingly, when H2O2 was injected into the EFM-HC system as an additional oxidant, the reactor performance gradually decreased as the dosing ratio increased; thus, the remaining experiments were performed without H2O2. Subsequently, an optimization process was conducted using response surface methodology with a Box-Behnken design. The inlet pressure, initial pH, applied voltage, and reaction time were chosen as operational key factors, while decolorization was selected as the response variable. The overall performance revealed that the selected parameters were either slightly interdependent, or had significant interactive effects on the decolorization. In the verification test, complete decolorization was observed under statistically optimized conditions. This study suggests that EFM-HC is a useful method for pretreatment of dye wastewater with positive economic and commercial benefits.

Application and optimization of electric field-assisted ultrasonication for disintegration of waste activated sludge using response surface methodology with a Box-Behnken design.

In the present study, an electric field is applied in order to disintegrate waste activated sludge (WAS). As a preliminary step, feasibility tests are investigated using different applied voltages of 10-100V for 60min. As the applied voltage increases, the disintegration degrees (DD) are gradually enhanced, and thereby the soluble N, P, and carbohydrate concentrations increase simultaneously due to the WAS decomposition. Subsequently, an optimization process is conducted using a response surface methodology with a Box-Behnken design (BBD). The total solid concentration, applied voltage, and reaction time are selected as independent variables, while the DD is selected as the response variable. The overall results demonstrate that the BBD with an experimental design can be used effectively in the optimization of the electric field treatment of WAS. In the confirmation test, a DD of 10.26±0.14% is recorded, which corresponds to 99.1% of the predicted response value under the statistically optimized conditions. Finally, the statistic optimization of the combined treatment (electric field+ultrasonication) demonstrated that even though this method is limited to highly disintegrated WAS when it is applied individually, a high DD of 47.28±0.20% was recorded where the TS concentration was 6780mg/l, the strength of ultrasonication was 8.0W, the applied voltage was 68.4V, and the reaction time was 44min. E-SEM images clearly revealed that the application of the electric field is a significant alternative method for the combined treatment of WAS. This study was the first attempt to increase disintegration using the electric field for a combined treatment with ultrasonication.

Development of a novel electric field-assisted modified hydrodynamic cavitation system for disintegration of waste activated sludge.

In this current study, we present a modified hydrodynamic cavitation device that combines an electric field to substitute for the chemical addition. A modified HC system is basically an orifice plate and crisscross pipe assembly, in which the crisscross pipe imparts some turbulence, which creates collision events. This study shows that for maximizing disintegration, combining HC system, which called electric field-assisted modified orifice plate hydrodynamic cavitation (EFM-HC) in this study, with an electric field is important. Various HC systems were compared in terms of disintegration of WAS, and, among them, the EFM-HC system exhibited the best performance with the highest disintegration efficiency of 47.0±2.0% as well as the destruction of WAS morphological characteristics. The experimental results clearly show that a conventional HC system was successfully modified. In addition, electric field has a great potential for efficient disintegration of WAS for as a additional option in a combination treatment. This study suggests continued research in this field may lead to an appropriate design for commercial use.

Quartz crystal microbalance sensor coated with nano-sized polystyrene latex spheres for SO2 detection.

In order to investigate the effect of surface morphology on the sensing performance in detecting sulfur dioxide, two different types polystyrene, polystyrene latex spheres (PLS) and polystyrene film (PSF), are synthesized by using an emulsion polymerization, which are coated on quartz crystal microbalance (QCM) surfaces. It is found that the sensing performance is strongly dependent on the morphology of polymer materials. The adsorption capacity of the synthesized PLS is higher than that of the PSF. In addition, the response of the PLS coated QCM to SO2 is approximately 6 times faster than that of the PSF coated one. The adsorption characteristics of SO2 on the PLS coated QCM are also evaluated in terms of temperature and concentration. These results show that the PLS can be used as SO2 sensor materials due to their high sensitivity and quick response.

Synthesis and characterization of monodispersed core-shell/polystyrene-silica composite nanospheres as artificial dusts.

Monodispersed core-shell/polystyrene-silica composite nanospheres are synthesized as artificial dusts by a two-step process, the preparation of seed copolymer spheres and the formation of a silica layer on the seed spheres. The poly(styrene-co-MPS) copolymer spheres containing silanol groups are first prepared by emulsion polymerization using 3-(trimethoxysilyl)propyl methacrylate (MPS) as a co-monomer, potassium persulfate (KPS) as a initiator, and sodium dodecyl sulfate (SDS) as a stabilizer. The diameter of the copolymer spheres is in the range of 220-270 nm with very small coefficients of variation (CV), depending on the content of MPS. The thermal property of the copolymer spheres is also improved as the content of silica increases. Later a silica layer is formed on the seed copolymer spheres by a reaction with tetraethylorthosilicate (TEOS) in aqueous solution. The thickness of the silica layer formed is about 4 to 10 nm, which greatly improves the thermal stability of the copolymer spheres.

A quartz crystal microbalance-based sensor system coated with functional polymers for SO2 and NO2 detection.

In this work, a quartz crystal microbalance (QCM)-based adsorption sensor system with high sensitivity, selectivity, and reproducibility is designed and fabricated. The functional polymers such as polypyrrole, poly(3,4-ethylenedioxythiophene) (PEDOT), and polystyrene are coated on 8 MHz AT-cut quartz crystal surfaces as sensing materials for SO2 and NO2. All sensing materials on the QCM surface are characterized experimentally by SEM and AFM. The frequency shifts of the QCM by adsorption and desorption of gases are measured and analyzed to assess the practical applicability of the sensor system. The overall results show that the QCM coated with polypyrrole is highly selective for SO2 gas and that coated with PEDOT is for NO2. It is proven that the QCM-based adsorption sensor system is possible for monitoring SO2 and NO2 gases in the mixture of ppm level.

Preparation of molecularly imprinted polymers for the detection of aromatic hydrocarbons.

In this study, the molecularly imprinted polymers (MIPs) are designed to improve their sensitivity and selectivity for specific aromatic hydrocarbons such as benzene, toluene, and xylene isomers. The MIPs based on methyl acrylate (MA) monomer are prepared using toluene and ethylene glycol dimetacrylate (EGDMA) as a template and a cross linking agent, respectively. The binding sites on the MIPs are characterized by using Fourier transform infrared spectrometry (FT-IR), nitrogen adsorption isotherms, and transmission electron microscopy (TEM). The selective behaviors of the MIPs are evaluated by their adsorption properties on a gravimetric apparatus. It is found that the performance is strongly influenced by the composition ratios of cross-linker, functional monomer, and template molecule. The molecular recognition ability can be assessed on the basis of an imprinting effect. The results indicate that the prepared MIPs can be used for the aromatic hydrocarbon sensor materials with high sensitivity and selectivity.

Adsorption and thermo desorption characteristics of hydrocarbons on single walled carbon nanotubes.

We investigated the heterogeneous adsorption and thermal desorption behaviors of acetone, n-hexane and trichloroethylene (TCE) on single walled carbon nanotubes (SWCNTs). Adsorption isotherms for selected molecules on SWCNTs were measured using a quartz spring balance at temperatures ranging from 303.15 to 323.15 K. Thermal gravimetric desorption experiments were also conducted at different heating rates (2-10 K/min) to obtain information about the interaction strength of hydrocarbons with SWCNTs surfaces. The adsorption isotherm data were analyzed successfully with the temperature dependent Toth equation. To obtain the adsorption and desorption energy distribution functions (AED/DED) for hydrocarbons and nitrogen, the integral equation with Fowler-Guggenheim isotherm (for AED) and first order desorption rate equation (for DED) were solved using the generalized nonlinear regularization method. It was found that Henry's constants, the isosteric heats of adsorption, and the pattern of energy distribution function were highly dependent on the polarizability.