Novel design of amine and metal hydroxide functional group modified onto sludge biochar for arsenic removal.

This study involved novel-designed sludge biochar (SB) adsorbed for arsenic removal with lower operating costs and higher adsorption efficiency properties. Generally, biochar only relies on micropores for pollutant adsorption, but physical adsorption is not highly efficient for arsenic removal. Therefore, in order to improve the removal efficiency of arsenic by SB, diethylenetriamine (DETA) and FeCl3 were used in this study to modify the surface of SB by an immersion method. The objectives of this research are to obtain optimum operation conditions by assessing the effect of different Fe content, pH and initial concentration on adsorbing arsenic. This study is the first to use Density Functional Theory (DFT) to simulate and verify the adsorption mechanism of arsenic by SB. Results showed the presence of amine/iron oxyhydroxides functional groups greatly promoted SB surface activity and its arsenic adsorption potential. The surface area, pore volume and pore size of the SB were estimated to be 525 m2 g-1, 0.35 cm3 g-1 and 8.71 nm, respectively. The DFT model result is the same as the result of arsenic adsorption performance with high adsorption energy (-246.3 kJmol-1) and shorter bond distances (1.42 Å), indicating strong chemical adsorption between arsenic and material. The reaction mechanism is divided into four pathways, including oxidation-reduction, complexation, electrostatic adsorption and pore adsorption.

Rich d-Fructose-Containing Polysaccharide Isolated from Myxopyrum smilacifolium Roots toward a Superior Antioxidant Biomaterial.

The presented study attempts to unveil and evaluate the antioxidant activity of a novel heteropolysaccharide separated from the roots of Myxopyrum smilacifolium (denoted as PS-MSR). The molecular weight of PS-MSR is found to be 1.88 × 104 Da and contains two principal sugars, which are d-glucose and d-fructose, in the backbone. Decoding the structure of the obtained PS-MSR sample has disclosed a novel polysaccharide for the first time. Indeed, the PS-MSR is composed of (1 → 3)-linked glucosyl units and (2 → 3)-linked fructosyl units. In addition, the 1D and 2D NMR spectra of the PS-MSR sample display the repeating unit of the isolated polysaccharide, [→3)-α-d-Glcp-(1 → 3)-ß-d-Frucf-(2 → 3)-ß-d-Frucf-2 → 3)-)-ß-d-Frucf-ß-(2→] n . Interestingly, the PS-MSR sample exhibits outstanding antioxidant activity, signifying the potential utilization of the explored polysaccharide for antioxidant-based material.

Preparation of Metal Modified onto Biochar from Hazardous Waste for Arsenic Removal.

Use of urban sludge, hospital sludge, and aquatic product sludge as a biochar adsorbent from wastewater treatment plants was investigated. Microwave carbonization was used to carbonize the sludge and then chemically activated at high temperatures to increase porosity and surface area. Effective of arsenic adsorption in water presents a newly designed metal doped to biochar. The biochar was characterized by scanning electron microscope (SEM) with energy dispersive X-ray (EDS), nitrogen adsorption/desorption isotherm analyzer (BET), thermo gravimetric analysis (TGA) and X-ray diffraction (XRD) analysis. Results display uniform pore sizes and high surface area (>490 m²g-1) of the biochar. Thence, urban sludge, hospital sludge, and aquatic product sludge can be used as carbon sources. The highest amount of Fe, Mn, and Ni loading onto the biochar was determined to be 8.0%, 6.0% and 10.0%, respectively. All biochar samples have arsenic adsorption capacities positively correlated with initial concentration. The corresponding removal efficiency of As(V) is 98% and As(III) is 84% at pH 3 with an adsorption capacity of 4.12 and 3.6 mg g-1, respectively. The adsorption capacity of As(V) and As(III) clearly decreased in the presence of PO43- (2.34 and 1.46 mg g-1, respectively). Due to competition for adsorption sites, the PO43- can effectively reduce arsenic adsorption. The arsenic species adsorption-desorption recycles on biochar are also discussed.

Polymer-free hydrogel made of lipid nanocapsules, as a local drug delivery platform.

Nanoparticle-loaded hydrogels are attractive pharmaceutical drug delivery systems that combine the advantages of both hydrogel (local administration and/or sustained drug release) and nanoparticle (stealthiness, targeting and decreased toxicity). The design of nanoparticle-loaded hydrogels is largely conventional, consisting of the dispersion of nanoparticles in a natural or synthetic polymer matrix to form a gel network. Novel nanoparticle-loaded hydrogels architecture could provide advantages in terms of innovation and application. We focused on the development of lipid nanocapsule (LNC)-based hydrogels without the use of a polymer matrix as a platform for drug delivery. Cytidine was modified by grafting palmitoyl chains (CytC16) and the new entity was added during the LNC phase-inversion formulation process allowing spontaneous gelation. Positioned at the oil/water interface, CytC16 acts as a crosslinking agent between LNCs. Association of the LNCs in a three-dimensional network led to the formation of polymer-free hydrogels. The viscoelastic properties of the LNC-based hydrogels depended on the LNC concentration and CytC16 loading but were not affected by the LNC size distribution. The LNC and drug-release profiles were controlled by the mechanical properties of the LNC-based hydrogels (slower release profiles correlated with higher viscoelasticity). Finally, the subcutaneous administration of LNC-based hydrogels led to classic inflammatory reactions of the foreign body-reaction type due to the endogenous character of CytC16, shown by cellular viability assays. New-generation nanoparticle-loaded hydrogels (LNC-based polymer-free hydrogels) show promise as implants for pharmaceutical applications. Once LNC release is completed, no gel matrix remains at the injection site, minimizing the additional toxicity due to the persistence of polymeric implants. Sustained drug-release profiles can be controlled by the mechanical properties of the hydrogels and could be tailor-made, depending on the therapeutic strategy chosen.

Adsorption Configurations of Iron Complexes on As(III) Adsorption Over Sludge Biochar Surface.

Waste recycling and reuse will result in significant material and energy savings. In this research, usage of hospital sludge as a biochar adsorbent for wastewater treatment plants was investigated. Microwave carbonization was used to carbonize the sludge and then chemically activated with ZnCl2to increase surface area and porosity. A newly designed iron metal doped sludge biochar carbon (SBC) has effective adsorption of inorganic arsenic (As(III), As2O3) in water. The findings clearly demonstrate the viability and utility of using hospital sludge as a source of carbon to generate SBC. The adsorption mechanism of As(III) on SBC's iron-metal-modified surface has been studied using density functional theory (DFT) to understand the impact of functional complexes on adsorption As(III). Tests showed physical as well as chemical adsorption of As(III) on Fe-SBC surface. Fe's involvement in functional complexes greatly fostered SBC surface activity and it's As(III) adsorption ability. The physical adsorption energies of As(III) with Fe functional complexes on the SBC surface were -42.3 KJ mol-1. Other hand, the chemical adsorption energies of As(III) on Fe-SBC surface was -325.5 KJ mol-1. As(III) is capable of interacting in a bidentate fashion with the dopants through the protonated oxygen atoms and this conformation of the cyclic structure is higher in the adsorption energy than the others.

Aqueous Oxytetracycline and Norfloxacin Sonocatalytic Degradation in the Presence of Peroxydisulfate with Multilayer Sheet-Like Zinc Oxide.

Multilayer ZnO sheet-like flakes were synthesized by a simple method of precipitation and characterized by the techniques of X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). The findings are proven that the SEM images show the overall morphology of a single sheet-like ZnO nanostructure made from uniformly thick nano-sheets. In an aqueous environment, the acoustic ability of the prepared material was assessed using ultrasound (US) radiation to degrade oxytetracycline (OTC) and norfloxacin (NF). To increase the degradation efficiency, a US/ZnO/peroxodisulfate system was developed by introducing ammonium persulfate ((NH4)2S2O8) and sodium persulfate (Na2S2O8), exhibiting excellent synergistic effects. Result show the decomposition efficiency for NF removal with Na2S2O8 (64%) appeared to be slightly better than with (NH4)2S2O8 (56%). By contrast, the ultrasonic catalytic efficiency of Na2S2O8 (98%) was slightly better than that of (NH4)2S2O8 (94%) for OTC removal. The addition of scavengers to the US/ZnO/peroxodisulfate system through the NF and OTC results in the largest effect of holes. The degradation is considered to be often caused by holes. In this system, the Na2S2O8 can have two roles to increase the rate of degradation: (1) The SO4- formed by Na2S2O8 under ultrasonic irradiation directly degraded to norfloxacin on ZnO surface; and (2) S2O82- behaved as an electron acceptor, inhibiting recombination of electron hole pairs, enabling the development of more ·OH. Therefore, the synergistic effect significantly increases US/ZnO/peroxodisulfate sonocatalytic activity (Hu, S.B., et al., 2017. Aqueous norfloxacin sonocatalytic degradation with multilayer flower-like ZnO in the presence of peroxydisulfate. Ultrasonics Sonochemistry, 38(1), pp.446-454).