Improved fractionation method using amphipathic NDAM for the efficient separation of disinfection by-product precursors in natural organic matter.

The hydrophilic substances in natural organic matter (NOM) are the main precursor of disinfection by-products (DBPs) formed during disinfection processes. The fractionation of the components in NOM based on hydrophilicity contributes to elaborating the behavior of NOM during disinfection. However, the traditional NOM fractionation method using two hydrophobic resins of DAX-8 and XAD-4 lays emphasis on the separation of hydrophobic substances, limiting the thorough study of the hydrophilic components in NOM. In this work, the amphiphilic resin NDAM was employed as a replacement of XAD-4 to realize more thorough separation of the hydrophilic substances. Compared with the divinylbenzene (DVB) structure of XAD-4, the NDAM possesses a more hydrophilic skeleton of N-vinylpyrrolidone (NVP) and DVB which favors the adsorption of hydrophilic components in NOM. The two fractionation methods of DAX-8 + XAD-4 and DAX-8 + NDAM were applied to fractionate NOM, and the obtained fractions were characterized via fluorescence spectra, UV spectra, acid-base titration, the partition coefficients of aqueous two-phase systems(ATPs), and 1H nuclear magnetic resonance (1H-NMR). The results showed that the transphilic fractions separated by XAD-4 accounted for 11.09% of NOM, while the proportion increased to 20.33% with the method of NDAM fractionation. Besides, the hydrophilic components enriched by NDAM not only have more π-conjugated systems and more aromatic structure but also contain more oxygen-containing and nitrogen-containing functional groups. In addition, the hydrophilic fractions separated by NDAM contained more DBP precursors. The NDAM separates more NOM which can produce bromine-containing DBPs into HPIA, and the DBP productivity of HPIN is significantly higher than that of XAD-4. In general, the NOM fractionation method proposed in this study utilizing NDAM resin could fractionate the hydrophilic fractions in NOM more thoroughly, showing application potential in the analysis and control of DBPs formed from NOM.

The roles of gold and silver nanoparticles on ZnIn2S4/silver (gold)/tetra(4-carboxyphenyl)porphyrin iron(III) chloride hybrids in carbon dioxide photoreduction.

The construction of hybrid catalysts composed of inorganic semiconductors and molecular catalysts shows great potential for achieving high photocatalytic carbon dioxide (CO2) conversion efficiency. In this study, ZnIn2S4 was first synthesized via a solvothermal route. Gold (Au) and silver (Ag) nanoparticles were then deposited on ZnIn2S4 via the reduction of noble metal precursor by sulfur vacancy defects. The obtained composite was further combined with tetra(4-carboxyphenyl)porphyrin iron(III) chloride (FeTCPP) molecular catalyst for efficient photocatalytic CO2 conversion. The roles of different noble metal nanoparticles in charge separation and interfacial electron transfer have been comprehensively studied. The photocatalytic performance and photoelectrochemical characterizations demonstrate that the introduction of Ag or Au nanoparticles is beneficial for charge separation. More importantly, the presence of Ag nanoparticles plays a crucial role in promoting the interfacial charge transfer between ZnIn2S4 and FeTCPP, whereas, Au nanoparticles function as active sites for the water reduction reaction.

Differential adsorption of zwitterionic PPCPs by multifunctional resins: The influence of the hydrophobicity and electrostatic potential of PPCPs.

Zwitterionic pharmaceuticals and personal care products can interact with adsorbents in different ways due to their various properties. In this work, the effects of hydrophobicity and electrostatic potential were explored through the adsorption of ciprofloxacin (CPX) and tetracycline (TC) onto multifunctional resins. Nonionic surface interaction was dominant for the adsorption on high-surface-area resin GMA10. Thereinto, hydrophobic and π-π interaction dominant for hydrophobic CPX and hydrophilic TC, respectively. Electrostatic interaction played an important role for high-anion-exchange-capacity resin GMA90. Upon their adsorption onto GMA50 resin, the relatively separated positive and negative electrostatic potentials of CPX+- due to the greater distance (∼12.33 Å) between the anionic and cationic groups led to electrostatic attraction and interaction (Ea = 8.64 ±â€¯0.31 kJ/mol) and the vertical orientation of molecule on the surface. However, TC+-0 displayed nonionic surface interaction (Ea = 7.96 ±â€¯0.14 kJ/mol) due to its relatively neutral electrostatic potential arising from the adjacent functional groups. Hence, the surface of GMA50 was covered with TC+-0 molecules adsorbed parallel to the surface, thereby restricting TC+-0 adsorption. Coexisted with monovalent salts, CPX adsorption was facilitated due to the salting-out effect. By contrast, the salting-out effect for TC was extremely weak, and TC adsorption was restrained due to the competitive adsorption of salts.

Degradation of benzophenone-4 in a UV/chlorine disinfection process: Mechanism and toxicity evaluation.

This study investigated the degradation of benzophenone-4 (BP-4) in a UV/chlorine disinfection process, with chlorination and UV disinfection as comparisons. With a degradation efficiency of 80% after 10 s, the UV/chlorine process significantly enhanced the degradation of BP-4. However, a rebound of 36% of the initial concentration was observed in the UV/chlorine process ([free active chlorine (FAC)]0:[BP-4]0 = 1:1, pH = 7). The same tendency appeared under the addition of alkalinity, Cl-, and humic acid (HA). This work interpreted this interesting kinetic tendency from the perspective of mechanism. In fact, the transformation between the chlorinated product P1 and BP-4 was reversible under certain conditions. The inhomogeneous charge distribution of the CCl bond in P1 led to the photolytic dechlorination of P1. This transformation caused an increase in BP-4 concentration. In addition, the increase in the UV light power promoted the photodecomposition of P1 under the experimental condition. In addition, this study evaluated the change in absorbable organic halogens (AOX) and three kinds of toxicity changes in the BP-4 solution after chlorination and the UV/chlorine process, including the acute toxicity of luminescent bacteria, endocrine disrupting effect and cytotoxicity. The UV/chlorine process exhibited lower ecotoxicity than chlorination in water treatment.

In vitro and in vivo studies of ultrafine-grain Ti as dental implant material processed by ECAP.

The aim of this study was to investigate the surface characterization of ultrafine-grain pure titanium (UFG-Ti) after sandblasting and acid-etching (SLA) and to evaluate its biocompatibility as dental implant material in vitro and in vivo. UFG-Ti was produced by equal channel angular pressing (ECAP) using commercially pure titanium (CP-Ti). Microstructure and yield strength were investigated. The morphology, wettability and roughness of the specimens were analyzed after they were modified by SLA. MC3T3-E1 osteoblasts were seeded onto the specimens to evaluate its biocompatibility in vitro. For the in vivo study, UFG-Ti implants after SLA were embedded into the femurs of New Zealand rabbits. Osseointegration was investigated though micro-CT analysis, histological assessment and pull-out test. The control group was CP-Ti. UFG-Ti with enhanced mechanical properties was produced by four passes of ECAP in BC route at room temperature. After SLA modification, the hierarchical porous structure on its surface exhibited excellent wettability. The adhesion, proliferation and viability of cells cultured on the UFG-Ti were superior to that of CP-Ti. In the in vivo study, favorable osseointegration occurred between the implant and bone in CP and UFG-Ti groups. The combination intensity of UF- Ti with bone was higher according to the pull-out test. This study supports the claim that UFG-Ti has grain refinement with outstanding mechanical properties and, with its excellent biocompatibility, has potential for use as dental implant material.

Power Conversion Efficiency and Device Stability Improvement of Inverted Perovskite Solar Cells by Using a ZnO:PFN Composite Cathode Buffer Layer.

We have demonstrated in this article that both power conversion efficiency (PCE) and performance stability of inverted planar heterojunction perovskite solar cells can be improved by using a ZnO:PFN nanocomposite (PFN: poly[(9,9-bis(3'-(N,N-dimethylamion)propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctyl)-fluorene]) as the cathode buffer layer (CBL). This nanocomposite could form a compact and defect-less CBL film on the perovskite/PC61BM surface (PC61BM: phenyl-C61-butyric acid methyl ester). In addition, the high conductivity of the nanocomposite layer makes it works well at a layer thickness of 150 nm. Both advantages of the composite layer are helpful in reducing interface charge recombination and improving device performance. The power conversion efficiency (PCE) of the best ZnO:PFN CBL based device was measured to be 12.76%, which is higher than that of device without CBL (9.00%), or device with ZnO (7.93%) or PFN (11.30%) as the cathode buffer layer. In addition, the long-term stability is improved by using ZnO:PFN composite cathode buffer layer when compare to that of the reference cells. Almost no degradation of open circuit voltage (VOC) and fill factor (FF) was found for the device having ZnO:PFN, suggesting that ZnO:PFN is able to stabilize the interface property and consequently improve the solar cell performance stability.