Synthesis and fabrication of magnetically separable phosphate-modified magnetic chitosan composites for lead(II) selective removal from wastewater.

To address the urgent need for efficient removal of lead-containing wastewater and reduce the risk of toxicity associated with heavy-metal wastewater contamination, materials with high removal rates and easy separation must be developed. Herein, a novel organic-inorganic hybrid material based on phosphorylated magnetic chitosan (MSCP) was synthesized and applied for the selective removal of lead (II) from wastewater. From the characterization and the experimental results can be obtained that the magnetic saturation strength of MSCP reaches 14.65 emu/g, which can be separated quickly and regenerated readily, and maintains high adsorption performance even after 5 cycles, indicating that the adsorbent possesses good magnetic separation performance and durability. Also, MSCP showed high selective adsorption performance for lead in the multiple metal ions coexistence solutions at pH 6.0 and room temperature, with an adsorption coefficient SPb-MSCP of 78.85%, which was much higher than that of MSC (the SPb-MSC was 11.59%). Additionally, in the single lead system, the sorption characteristics of Pb(II) on MSCP and MCP had obvious pH-responsiveness, and their adsorption capacity increased with the increase of solution pH, reaching the maximal values of 80.19 and 72.68 mg/g, respectively. It is noteworthy that the acid resistance of MSCP with an inert layer coated on the core is significantly improved, with almost no iron leaching from MSCP over the entire acidity range, while MCP has 7.63 mg/g of iron leaching at pH 1.0. Significantly, MSCP exhibited a maximum adsorption capacity of 102.04 mg/g, which matches the Langmuir model at pH 6.0 and 298.15 K, and points to the pseudo-second-order kinetics of the chemisorption process of Pb(II) on MSCP. These findings highlight the great potential of MSCP for Pb(II) removal from aqueous solution, making it a promising solution for Pb(II) contamination in wastewater.

Efficient removal of RR2 dye by electro- Ce(III) process with its elegant arts and attractive charm in performance, energy consumption and mechanism.

Reactive red 2 (RR2) azo dye wastewater poses a serious hazard to the water environment health, so using a novel and efficient Electro- Ce(III) (E- Ce(III)) process takes on a critical significance in treating RR2 dye wastewater. In this study, the effects of a variety of single-factor conditions on RR2 removal efficiency were evaluated in depth. The results indicated that the optimal experimental conditions are as reaction temperature of 25 °C, Na2SO4 concentration of 25 mM, Ce(III) concentration of 0.3 mM, pH of 4.0, and current density of 40.0 mA/cm2. When the RR2 dye wastewater was treated for 40 min under the optimal experimental conditions, a high removal rate of 99.8% for RR2 was obtained. It is suggested that the background ion PO43- in the dye wastewater inhibits the E-Ce (III) process, whereas Cl- facilitates this process. Moreover, the yield of Ce(IV) increases with the increase of the current density. At the current density of 40.0 mA/cm2, a reasonable energy consumption of 3.85 kW h/gTOC for the process was obtained after the 3-h treatment. The effects of different degradation processes (including Direct Electrooxidation (DEO), single Ce(III), and E-Ce (III)) on RR2 removal efficiency and TOC change were compared. The types of oxidizing substances in the E-Ce (III) process were detected, and the mechanism of RR2 oxidative degradation in the E-Ce (III) process was summarized. The result suggests that the E-Ce (III) process has low power consumption. Meanwhile, in the E-Ce (III) process, free reactive Ce(IV) with strong oxidation is continuously generated, RR2 can be efficiently degraded. And the continuous cycle transformation between Ce(III) and Ce(IV) maintains the strong oxidation of the process. The contribution of free reactive Ce(IV) and DEO to RR2 degradation was obtained as 58.8% and 39.8%, respectively. The combined effect of Ce(IV) and DEO played a major role in the E-Ce (III) process, while ·OH exhibited a relatively weak effect (nearly 1.4%). RR2 was comprised of 13 major intermediates, and the biodegradability of wastewater was improved significantly after treatment, thus facilitating the further mineralization and biodegradation of the products. The E- Ce(III) process is novel, efficient, and environment-friendly, and has a large market application space, suggesting that it can be applied as an efficient, economic, and sustainable water treatment process.

Study on the performance efficiency, mechanism, power consumption and biochemical properties of E/Ce(IV)/PMS on the enhanced removal of RB19.

In this study, an advanced oxidation process with E/Ce(IV) synergistic PMS (E/Ce(IV)/PMS) was established for the efficient removal of Reactive Blue 19 (RB19). The catalytic oxidation performance of different coupling systems was examined and the synergistic effect of E/Ce(IV) with PMS in the system was substantiated. The oxidative removal of RB19 in E/Ce(IV)/PMS was excellent, achieving a removal efficiency of 94.47% and a reasonable power consumption (EE/O value was 3.27 kWh·m-3). The effect of pH, current density, Ce(IV) concentration, PMS concentration, initial RB19 concentration and water matrix on the removal efficiency of RB19 were explored. Additionally, quenching and EPR experiments showed that the solution contains different radicals such as SO4·-, HO∙ and 1O2, where 1O2 and SO4·- played key roles, but HO∙ just acted a weaker role. Ce ion trapping experiment confirmed that Ce(IV) was involved in the reaction process and played a major role (29.91%). RB19 was subject to three possible degradation pathways, and the intermediate products displayed well biochemical properties. To conclude, the degradation mechanism of RB19 was explored and discussed. In the presence of current, E/Ce(IV)/PMS performed a rapid Ce(IV)/Ce(III) cycle, continuously generating strong catalytic oxidation Ce(IV), The reactive radicals derived from the decomposition of PMS, in conjunction with Ce(IV) and direct electro-oxidation, efficiently destroyed the molecular structure of RB19 and showed an efficient removal rate.

Effects of micro(nano)plastics on soil nutrient cycling: State of the knowledge.

The ecological impacts of micro(nano)plastics (MNPs) have attracted attention worldwide because of their global occurrence, persistence, and environmental risks. Increasing evidence shows that MNPs can affect soil nutrient cycling, but the latest advances on this topic have not systematically reviewed. Here, we aim to present the state of knowledge about the effects of MNPs on soil nutrient cycling, particularly of C, N, and P. Using the latest data, the present review mainly focuses on three aspects, including (1) the effects and underlying mechanisms of MNPs on soil nutrient cycling, particularly of C, N and P, (2) the factors influencing the effects of MNPs on soil nutrient cycling, and (3) the knowledge gaps and future directions. We conclude that MNPs can alter soil nutrient cycling via mediating soil nutrient availability, soil enzyme activities, functional microbial communities, and their potential ecological functions. Furthermore, the effects of MNPs vary with MNPs characteristics (i.e., polymeric type, size, dosage, and shape), chemical additives, soil physicochemical conditions, and soil biota. Considering the complexity of MNP-soil interactions, multi-scale experiments using environmental relevant MNPs are required to shed light on the effects of MNPs on soil nutrients. By learning how MNPs influence soil nutrients cycles, this review can guide policy and management decisions to safeguard soil health and ensure sustainable agriculture and land use practices.

Electrically supported mediator Co(II)-activated peroxydisulfate synergistic process for organic contaminants elimination.

Among homogeneous catalysts, cobalt ions exhibit ultra-high persulfate activation performance. In this work, an electrically supported medium Co(II) activated peroxydisulfate synergistic process was established to eliminate organic contaminants in water. The synergistic catalytic effect was verified by comparing the oxidative degradation performance and reaction rate constant of different coupling systems. The decolorization ability of E-Co(II)-PDS on reactive black 5 (RB5) was explored, and the results showed that the removal rate of RB5 can reach 93.21% under the optimized conditions of current density of 5.71 mA/cm2, initial pH of 4, Co(II) concentration of 0.2 mM and PDS concentration of 5 mM. The effect of water matrix on the removal of RB5 was studied, and it was found that HCO3- and humic acid significantly inhibited the degradation of RB5, while Cl- and H2PO4- could effectively promote it at a certain concentration. Notably, the degradation of RB5 in E-Co(II)-PDS system achieved lower energy consumption, with an energy consumption per unit volume (EE/O) value of 0.4304 kWh·m-3. EPR test, quenching experiments and contribution rate analysis showed that the oxidation active species in E-Co(II)-PDS process were Co(III), sulfate radicals and hydroxyl radicals, and their oxidation contribution rates were 15.72%, 12.69% and 53.25%, respectively. Finally, the decomposition process of RB5 was proposed by the mass spectrometry results. The electric current promotes cobalt ion cycling and PDS activation through electron transfer, and induces Co(II) to promote the activation of PDS, which is the main mechanism of E-Co(II)-PDS system to achieve the robust degradation ability of RB5.

Conformational Equilibria of 2-Methoxypyridine⋠⋠⋠CO2 : Cooperative and Competitive Tetrel and Weak Hydrogen Bonds.

The rotational spectrum of 2-methoxypyridine⋅⋅⋅CO2 was recorded and analysed employing a cavity-based Fourier transform microwave spectrometer, complemented with quantum chemical calculations which predicted three possible isomers within energies less than 1000 cm-1 . The two most stable isomers were observed in the pulsed jet, which are stabilized by a network of C⋅⋅⋅N/O tetrel and C-H⋅⋅⋅O weak hydrogen bonds. The relative population ratio of the two detected isomers was estimated to be NI /NII ≈2.5. The competition and cooperation of the present non-covalent interactions in both isomers are discussed within the framework of Bader's quantum theory of atoms in molecules and Johnson's non-covalent interaction analyses. The study shows, that when looking for CO2 adsorbents, one might prefer candidates with multiple interactions in one site over candidates with few but strong interactions.

Competitive and cooperative n →π* and n →σ* interactions in benzaldehyde-formaldehyde: rotational characterization.

The rotational spectrum of the 1 : 1 benzaldehyde-formaldehyde complex has been investigated by pulsed jet Fourier transform microwave spectroscopy combined with ab initio calculations. The two most stable isomers were observed, with the relative abundance ratio NI/NII≈ 3/1 estimated with intensity measurements. Both observed isomers are stabilized by one dominating O[double bond, length as m-dash]CO tetrel bond (n →π* interaction) and one secondary C-HO hydrogen bond. Natural bond orbital analysis and electron localization function analysis were applied to characterize the nature of the noncovalent interactions in the target complex.

In Situ Regeneration of Phenol-Saturated Activated Carbon Fiber by an Electro-peroxymonosulfate Process.

Regeneration is required to restore the adsorption performance of activated carbon used as an adsorbent in water purification. Conventional thermal and electrochemical regenerations have high energy consumption and poor mineralization of pollutants, respectively. In this study, phenol-saturated activated carbon fiber was regenerated in situ using an electro-peroxymonosulfate (E-PMS) process, which mineralized the desorbed contaminants with relatively low energy consumption. The initial adsorbed phenol (81.90%) was mineralized, and only 4.07% of the initial concentration remained in the solution after 6 h of E-PMS regeneration. The phenol degradation was dominated by hydroxyl radical oxidation. Adding the PMS in three doses at 2 h intervals improves the regeneration performance from 75% to more than 82%. Regeneration retained 60% of its initial effectiveness even in the 10th cycle with 4.40% of the initial concentration of phenol remaining in the solution. These results confirm the E-PMS regeneration process as effective, sustainable, and environmentally friendly for regenerating activated carbon.

Effects of acid, acid-ZVI/PMS, Fe(II)/PMS and ZVI/PMS conditioning on the wastewater activated sludge (WAS) dewaterability and extracellular polymeric substances (EPS).

The effects of four conditioning approaches: Acid, Acid-zero-valent iron (ZVI)/peroxydisulfate (PMS), Fe(II)/PMS and ZVI/PMS, on wastewater activated sludge (WAS) dewatering and organics distribution in supernatant and extracellular polymeric substances (EPS) layers were investigated. The highest reduction in bound water and the most WAS destruction was achieved by Acid-ZVI/PMS, and the optimum conditions were pH 3, ZVI dosage 0.15 g/g dry solid (DS), oxone dosage 0.07 g/g DS and reaction time 10.6 min with the reductions in capillary suction time (CST) and water content (Wc) as 19.67% and 8.49%, respectively. Four conditioning approaches could result in TOC increase in EPS layers and supernatant, and protein (PN) content in tightly bound EPS (TB-EPS). After conditioning, organics in EPS layers could migrate to supernatant. Polysaccharide (PS) was easier to migrate to supernatant than PN. In addition, Acid, Acid-ZVI/PMS or Fe(II)/PMS conditioning promoted the release of some polysaccharides containing ring vibrations v PO, v C-O-C, v C-O-P functional groups from TB-EPS. ESR spectra proved that both radicals of SO4-· and ·OH contributed to dewatering and organics transformation and migration. CST value of WAS positively correlated with the ratios of PN/PS in LB-EPS and total EPS, while it negatively correlated with TOC, PN content and PS content in TB-EPS, as well as PS content in supernatant and LB-EPS. BWC negatively correlated to zeta potential and TOC value, PN content, and HA content in supernatant.

Generation of Active Mn(III)aq by a Novel Heterogeneous Electro-permanganate Process with Manganese(II) as Promoter and Stabilizer.

Our study on the synergetic effect of electrolysis and permanganate (E-PM) revealed a novel alternative method for generating active Mn(III)aq heterogeneously by electrochemically activating PM with Mn2+ as promoter and stabilizer. We systematically explored the generation mechanism of Mn(III)aq. It indicated that all three components (electrolysis + PM + Mn2+) were necessary to facilitate the generation of active Mn(III) in the E-PM-Mn2+ process. It was worth noting that Mn2+, as essential promoter and Mn(III)aq stabilizer, could considerably enhance the concentration of Mn(III) in the E-PM-Mn2+ process. Further study revealed that the active Mn(III) was mainly produced on cathode rather than in aqueous solution or on anode. In addition, the soluble Mn(III)aq generated in the E-PM-Mn2+ process was demonstrated to be very efficient for the degradation and mineralization of diclofenac (DCF) as well as methyl blue, carbamazepine, phenol, sulfamethoxazole, and nitrobenzene. Moreover, the effects of the main operating parameters (Mn2+ dosage, PM dosage, applied current density, pH of solution, and contaminant concentration) and different water matrices on the E-PM-Mn2+ process were investigated systematically. Possible degradation pathways of DCF in the E-PM-Mn2+ process were also proposed. The results demonstrated that the E-PM-Mn2+ system based on active Mn(III)aq could create a more efficient, sustainable, and less energy costing technology for water treatment.

Electrochemical degradation of oxytetracycline by Ti-Sn-Sb/γ-Al2O3 three-dimensional electrodes.

In this work, Ti-Sn-Sb/γ-Al2O3 particle electrodes were prepared and employed for the degradation of oxytetracycline (OTC) by three-dimensional electrocatalytic technology. Factors associated with the preparation of Ti-Sn-Sb/γ-Al2O3 particle electrodes were investigated. The effects of initial concentration, conductivity, pH value, aeration intensity, current density, plate spacing, and particle electrode dosage on OTC removal were studied. The removal rate of OTC and total organic carbon were achieved approximately 92.0% and 41.0% under the optimal operating condition, respectively. In addition, Ti-Sn-Sb/γ-Al2O3 particle electrode was analyzed by Fourier Transform Infrared spectroscopy (FT-IR), scanning electron microscope (SEM), energy dispersive spectrum analysis (EDX), X-Ray Fluorescence Spectrometer (XRF), and X Ray Diffraction analysis (XRD), which indicated that a significant amount of TiO2, SnO2, and Sb2O3 were formed on the surface of Ti-Sn-Sb/γ-Al2O3 particle electrode. It was also observed that the primary function of Ti-Sn-Sb/γ-Al2O3 particle electrode in the three-dimensional electrode electrolysis process is the strong oxidizing function of ·OH for degrading OTC. Consequently, the analysis of degradation products of oxytetracycline (OTC) demonstrates. In addition, the results and conclusions of this study provide a methodological basis and engineering practice basis for removing the low concentration of antibiotics in water.

Novel chitosan-based flocculants for chromium and nickle removal in wastewater via integrated chelation and flocculation.

Carboxylated chitosan (CPCTS) is used as substrates in the design and synthesis of CPCTS-based flocculants through UV-initiated polymerization techniques. The synthesized flocculants are applied to remove Cr and Ni ions from chromic acid lotion and electroplating wastewater through two-stage flocculation. This study investigates the effect of flocculant dosage, pH, reaction time, and stirring speed on the removal efficiency of Cr and Ni ions. Results indicated that the total Cr removal ratios by CPCTS-graft-polyacrylamide-co-sodium xanthate (CAC) and CPCTS-graft-poly [acrylamide-2-Acrylamido-2-methylpropane sulfonic acid] (CPCTS-g-P(AM-AMPS)) are 94.7% and 94.6%, respectively. The total Ni removal efficiencies by CAC and CPCTS-g-P(AM-AMPS) are 99.3% and 99.4%, respectively. The two-stage flocculation with CPCTS-based flocculants could reduce the total concentrations of Cr and Ni to 1.0 mg/L and 0.5 mg/L, respectively. The relationship of removal capacity and structural properties between the flocculants with different functional groups is established through Fourier transform infrared spectroscopy, nuclear magnetic resonance, scanning electron microscopy, and X-ray diffraction. The micro-interfacial behavior between the colloidal particles and the solution during the integrated chelation-flocculation are elucidated. Thus, CPCTS-based flocculants could be a potential material for the removal of high amounts of Cr and Ni ions in industrial wastewater.

Optimization and mechanism of Acid Orange 7 removal by powdered activated carbon coupled with persulfate by response surface method.

In this study, powder activated carbon (PAC) utilized to activate peroxydisulfate (PDS) was investigated for decolorization of Acid Orange 7 (AO7). The results indicated a remarkable synergistic effect in the PAC/PDS system. The effect of PAC, PDS dosages and initial pH on AO7 decolorization were studied and the processes followed first-order kinetics. Response surface method with central composite design (CCD) model was utilized to optimize these three factors and analyze the combined interaction. The optimum condition for the decolorization rate of AO7 was analyzed as the following: PAC (0.19 g/L), PDS (1.64 g/L), and initial pH (4.14). Cl- and SO4 2- showed a promoting effect on AO7 decolorization while HCO3 - had a slightly inhibiting effect. Quenching experiments confirmed that both sulfate and hydroxyl radicals were the oxidizing species, and the oxidation reaction occurred on the surface of PAC. The results of UV-vis spectrum with 100% decolorization rate and the 50% total organic carbon reduction indicated highly efficient decolorization and mineralization of AO7 in the PAC/PDS system. Finally, the recovery performance of PAC was studied and the result indicated PAC had poor reuse in reactivity.

Magnetic micro-particle conditioning-pressurized vertical electro-osmotic dewatering (MPEOD) of activated sludge: Role and behavior of moisture and organics.

In this study, a magnetic micro-particle conditioning-pressurized vertical electro-osmotic dewatering (MPEOD) process with magnetic micro-particle conditioning-drainage under gravity-mechanical compression-electrical compression (MMPC-DG-MC-EC) stages was established to study the distribution and migration of water, extracellular polymeric substances (EPS), and other organic matter in the activated sludge (AS) matrix at each stage. Results showed that the MPEOD process could attain 53.52% water content (WC) in dewatered AS with bound water (BW) and free water (FW) reduction rates of 82.97% and 99.67%, respectively. The coagulation and time-delayed magnetic field effects of magnetic micro-particles (MMPs) along the MMPC-DG-MC stages initiated the transformation of partial BW to FW in AS. EC had a coupling driving effect of electro-osmosis and pressure on BW, and the changes in pH and temperature at EC stage induced the aggregation of AS flocs and the release of partial BW. Additionally, MMPs dosing further improved the dewatering performance of AS by acting as skeleton builders to provide water passages. Meanwhile, MMPs could disintegrate sludge cells and EPS fractions, thereby reducing tryptophan-like protein and byproduct-like material concentrations in LB-EPS as well as protein/polysaccharide ratio in AS matrix, which could improve AS filterability. At EC stage, the former four Ex/Em regions of fluorescence regional integration analysis for EPS were obviously reduced, especially the protein-like substances in LB- and TB-EPS, which contributed to improvement of AS dewaterability.

Adsorption and photocatalytic degradation of pharmaceuticals and pesticides by carbon doped-TiO2 coated on zeolites under solar light irradiation.

To evaluate the performance of zeolite-supported carbon-doped TiO(2) composite catalysts toward target pollutants under solar light irradiation, the adsorption and photocatalytic degradation of 18 pharmaceuticals and pesticides with distinguishing features (molecular size and volume, and photolysis) were investigated using mordenite zeolites with SiO(2)/Al(2)O(3) ratios of 18 and 240. Different quantities of carbon-doped TiO(2) were coated on the zeolites, and then the finished composite catalysts were tested in demineralized, surface, and hospital wastewater samples, respectively. The composite photocatalysts were characterized by X-ray diffraction, field emission scanning electron microscopy, and surface area and porosity analyses. Results showed that a dispersed layer of carbon-doped TiO(2) is formed on the zeolite surface; this layer blocks the micropores of zeolites and reduces their surface area. However, these reductions did not significantly affect adsorption onto the zeolites. Our results demonstrated that zeolite-supported carbon-doped TiO(2) systems can effectively degrade 18 pharmaceuticals and pesticides in demineralized water under natural and simulated solar light irradiation. In surface and hospital wastewaters, zeolite-supported carbon-doped TiO(2) systems present excellent anti-interference capability against radical scavengers and competitive organics for pollutants removal, and higher pollutants adsorption on zeolites evidently enhances the removal rate of target pollutants in surface and hospital wastewater samples with a complicated matrix.

Reversibility of the structure and dewaterability of anaerobic digested sludge.

The reversibility of the structure and dewaterability of broken anaerobic digested sludge (ADS) is important to ensure the efficiency of sludge treatment or management processes. This study investigated the effect of continuous strong shear (CSS) and multipulse shear (MPS) on the zeta potential, size (median size, d50), mass fractal dimension (D(F)), and capillary suction time (CST) of ADS aggregates. Moreover, the self-regrowth (SR) of broken ADS aggregates during slow mixing was also analyzed. The results show that raw ADS with d50 of 56.5 µm was insensitive to CSS-SR or MPS-SR, though the size slightly decreased after the breakage phase. For conditioned ADS with d50 larger than 600 µm, the breakage in small-scale surface erosion changed to large-scale fragmentation as the CSS strength increased. In most cases, after CSS or MPS, the broken ADS had a relatively more compact structure than before and d50 is at least 200 µm. The CST of the broken fragments from optimally dosed ADS increased, whereas that corresponding to overdosed ADS decreased. MPS treatment resulted in larger and more compact broken ADS fragments with a lower CST value than CSS. During the subsequent slow mixing, the broken ADS aggregates did not recover their charge, size, and dewaterability to the initial values before breakage. In addition, less than 15% self-regrowth in terms of percentage of the regrowth factor was observed in broken ADS after CSS at average velocity gradient no less than 1905.6 sec(-1).

[Study on the Catalytic Kinetic Spectrophotometric Determination of Trace Amounts of Iron(â ¢) and Its Reaction Mechanism].

A catalytic kinetic spectrophotometric method, which is based on the catalytic effect of Fe(Ⅲ) on the fading reaction between potassium persulfate(K2S2O8) and methyl red(MR) in the solution of 0.30 mol·L-1 hydrochloric acid, for the determination of trace amounts of Fe(Ⅲ) has been investigated. A novel detection system, Fe(Ⅲ)-HCl-K2S2O8-MR, has been developed. The optimum experimental conditions for the determination of trace amounts of Fe(Ⅲ) were found on the basis of orthogonal test. The kinetics parameters and equation of this fading reaction of MR were studied. Its reaction mechanism was discussed. The results show that there is a good linear relationship between the variation of MR absorbance at the maximum absorption wavelength of 518 nm and the concentration of Fe(Ⅲ) under the optimum experimental conditions: ln(A0/A)=1.334 1+0.001 0, the correlation coefficient is 0.999 1. The kinetic research shows that the reaction order with respect to Fe(Ⅲ) is 1 and the overall fading reaction is a pseudo-first order reaction. The apparent activation energy of the fading reaction of MR is 69.88 kJ·mol-1. Furthermore, the catalytic effects of Fe(Ⅲ) on this fading reaction is confirmed by its reaction mechanism. This novel method for the determination of trace Fe(Ⅲ) has never previously been published so far. Trace amounts of Fe(Ⅲ) can be selectively determined by this catalytic kinetic spectrophotometric method with high precision and accuracy. This method is simple and its reagents used are cheap and available. Its sensitivity is higher than that of conventional spectrophtometry with detection limit of 0.005 mg·L-1. This detection system is stable. This proposed method has been applied to the determination of trace amounts of Fe(Ⅲ) in food and water samples with satisfactory results. Relative standard deviation of the detection results is 1.18%～2.11%. Average recovery rate of the detection results is 98.0%～104.0%.

[Study on the Preparation of A New Composite Coagulant: Poly-Ferric-Titanium-Sulfate and Analysis of FTIR Spectrum and UV-Vis Spectrum].

Composite coagulants have drawn a widespread attention recently for its superior coagulation-flocculation performance. Fe and Ti based coagulants, as a kind of inorganic metal water treatment agent, h have received huge attention, but there is little study about the preparation and characterization of composite coagulate composite with Ti4+. In this paper we prepared a composite coagulant, in which the Ti (SO4)2 was introduced as coordination complexes, PO3-4 as stabilizer and complexant. Then, the FT-Infra Red spectrum (FT-IR) and ultraviolet/visible absorption spectrum (UV-Vis) were adopted to characterizse the changes of chemical group, species distribution of coagulants in case of varies Ti/Fe, P/Fe and OH/Fe molar ratio. The results shows other than simple mixture of the raw materials, the introduction of Ti4+ and ­PO4 group synthesized the chemical group bond as Ti­O, ­Fe­P­Fe­ and ­Ti­P­Ti­, which were beneficial to the degree of polymerization and increased the stability of the product. Furthermore, when the Ti/Fe molar ratio of 1∶8, P/Fe was in the range of 0.2~0.3, the optimal material is suitable for the generation of Fe­P­Ti­ chemistry bond and medium polymer as Fe6(OH)6+12，[Fex(OH)y]2H2PO(6x-2y-1)+4. Whereas, too much addition of Ti4+, PO3-4 and HCO-3 deteriorated the polymer structure, leading to the presentation of precipitate as TiO2, Ti3(PO4)4 and FePO4, which will decrease the coagulation performance.

[The Preparation and Characterization of a New Solid Coagulant: Polymeric Ferric Silicate Sulfate].

As one of the most important water treatment agents, polysilicate coagulant, has been playing an important role in coagulation- flocculation, but it is prone to lose stability due to self-polymerization and the forming of silica gel. Therefore, research on the preparation of stable polysilicate coagulant has attract great attention. A new method to prepare a stable polysilicate coagulant (PSPF), was proposed in this paper. Its structure and morphology were characterized by using Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) respectively. Fe species in PSPF was analyzed via Fe-Ferron complexation timed spectrophotometric method. The performance of PSPF was assessed by measuring micro-polluted water treatment efficiency. Primary chemicals, such as ferrous sulfate, sodium silicate, potassium dihydrogen phosphate, sodium carbonate, were used. The influence of those parameters affecting the preparation of PSPF, such as nSi/nFe, nP/nFe and nOH/nFe molar ratios were examined. The results showed that nSi/nFe of 1∶4, nP/nFe of 1∶6 and nOH/nFe of 1∶10 under 60 ℃ water bath for 30 min was the optimum condition for preparation. The FTIR spectrum indicated that PSPF was a kind of high molecular polymer, containing new groups (e.g., Si­O­Si and Fe­O­Si), which could increase the molecular weight，molecular chain and coagulation-flocculation efficiency. PSPF presented a cluster appearance similar to a network structure, which was conductive to adsorption-bridging capacity and precipitation sweeping. The increase of Fe(b) and Fe(c) as a result of Si increasing in PSPF improved the polymerization and solidification. The coagulation behaviors of PSPF that were largely affected by the coagulant dosage and pH, indicated that for pH and dosage at 6 and 8 mg·L-1, respectively, the residual turbidity and UV254 removal efficiency could achieve 0.33 NTU and 58.6%, respectively.