Improper disposal of organic solid waste results in serious environmental pollution. Aerobic composting provides an environmentally friendly treatment method, but improving humification of raw materials remains a challenge. This study revealed the effect of different concentrations of potassium persulfate (PP) on humification of chicken manure and straw aerobic composting and the underlying microbial mechanisms. The results showed that when 0.6 % PP was added (PPH group), humus and the degree of polymerization were 80.77 mg/g and 2.52, respectively, which were significantly higher than those in 0.3 % PP (PPL group). As the concentration of PP was increased, the composition of rare taxa (RT) changed and improved in evenness, while abundant taxa (AT) was unaffected. Additionally, the density (0.037), edges (3278), and average degree (15.21) in the co-occurrence network decreased compared to PPL, while the average path (4.021) and modularity increased in PPH. This resulted in facilitating the turnover of matter, information, and energy among the microbes. Interestingly, cooperative behavior between microorganisms during the maturation period (24-60 d) occurred in PPH, but competitive relationships dominated in PPL. Cooperative behavior was positively correlated with humus (p < 0.05). Because the indices, such as higher degree, betweenness centrality, eigenvector centrality, and closeness centrality of the AT, were located in the microbial network center compared to RT, they were unaffected by the concentration of PP. The abundance of carbohydrate and amino acid metabolic pathways, which play an important role in humification, were higher in PPH. These findings contribute to understanding the relative importance of composition, interactions, and metabolic functionality of RT and AT on humification during chicken manure and straw aerobic composting under different concentrations of PP, as well as provide a basic reference for use of various conditioning agents to promote humification of organic solid waste.

n-Bu4NI/K2S2O8 mediated C-N coupling between aldehydes and amides is reported. A strong electronic effect is observed on the aromatic aldehyde substrates. The transformylation from aldehyde to amide takes place exclusively when an aromatic aldehyde bears electron-donating groups at either the ortho or para position of the formyl group, while the cross-dehydrogenative coupling dominates in the absence of these groups. Both the density functional theory (DFT) thermochemistry calculations and experimental data support the proposed single electron transfer mechanism with the formation of an acyl radical intermediate in the cross-dehydrogenative coupling. The n-Bu4NI/K2S2O8 mediated oxidative cyclization between 2-aminobenzamide and aldehydes is also reported, with four quinazolin-4(3H)-ones prepared in 65-99% yields.

Six derivatives of poly-N-vinylcaprolactam (PNVCL) P1-P6 were synthesized via surfactant-free precipitation polymerization (SFPP) at 70 °C, with potassium persulfate (KPS) as the initiator. P5 and P6 were synthesized using the cross-linker N,N\'-Methylenebisacrylamide (MBA). The conductivity was measured to monitor the polymerization process. The hydrodynamic diameters (HDs) and polydispersity indexes (PDIs) of aqueous dispersions of P1-P6 were determined using dynamic light scattering (DLS) and zeta potential (ZP) using electrophoretic mobilities. At 18 °C for P1-P6, the HDs (nm) were 428.32 ± 81.30 and PDI 0.31 ± 0.19, 528.60 ± 84.70 (PDI 0.42 ± 0,04), 425.96 ± 115.42 (PDI 0.56 ± 0.08), 440.34 ± 106.40 (PDI 0.52 ± 0.09), 198.39 ± 225.35 (PDI 0.40 ± 0.19), and 1201.52 ± 1318.05 (PDI 0.71 ± 0.30), the and ZPs were (mV) 0.90 ± 3.23, -4.46 ± 1.22, -6.44 ± 1.82, 0.22 ± 0.48, 0.18 ± 0.79, and -0.02 ± 0.39 for P1-P6, respectively. The lower critical solution temperature ranged from 27 to 29 °C. The polymers were characterized using the ATR-FTIR method. The study concluded that the physicochemical properties of the product were significantly affected by the initial reaction parameters. Polymers P1-P4 and P6 have potential for use as drug carriers for skin applications.

Vegetable waste (VW) is a potential organic fertilizer resource. As an important way to utilize vegetable wastes, aerobic composting of VW generally has the problems of long fermentation cycle and incomplete decomposition of materials. In this study, 0.3-1.2% of potassium persulfate (KPS) was added to promote the maturity of compost. The results showed that the addition of KPS promoted the degradation of materials, accelerated the temperature rise of compost. KPS also promoted the formation of humic substances (HS). Compared with the control, HS contents of treatments with KPS addition increased by 7.81 ~ 17.52%. Fourier transform infrared (FTIR) spectroscopy and scanning electron microscope (SEM) analysis reveal the mechanism of KPS affecting the composting process: KPS stimulated the degradation of various organic substances such as lignin at high temperature stage, and the degradation of lignin could accelerate the release and decomposition of other components; KPS made the structure of the material looser, with more voids and pores, and more specific surface area of the material, which was more suitable for microbial degradation activities. Therefore, the addition of KPS can promote the decomposition of organic matter in the early stage of composting, accelerate the process of thermophilic phase, and shorten the composting process and improve product maturity.

Energy conservation and emission reduction are the general trend of the present world. In this study, a catalyst of 3WSH based on the waste recycle of waterworks sludge (WS) and Chinese herbs was prepared using one-step calcination treatment and then characterized by SEM, XRD, XPS, FTIR and BET. The catalytic performance of 3WSHB for activating potassium persulfate (PDS) was evaluated through the degradation of Safranine T (ST) in the presence of boron powder (B). The effects of vital parameters on ST removal were systematically studied, including PDS concentration, 3WSHB dosage, initial solution pH, B dosage, temperature and coexisting cations. The highest efficiency of ST removal was up to 93.0% under the optimal condition with 1.85 mM of PDS, 0.3 g/L of 3WSHB, 0.35g/L of B, 7 of pH. EPR and free radical quenching experiments demonstrated that •OH was the dominant reactive oxygen species for ST degradation in the PDS/3WSHB/B system. Moreover, the intermediates determined by HPLC-MS indicated that the oxidization of benzene ring substituents in ST and a hydrogen abstraction by electron transfer might occur during ST degradation. The dissatisfied reuse performance of 3WSHB might be attributed to its low Fe content and simple reusing way. The results demonstrate the effectiveness of WS recycling and reuse in the field of pollutant remediation.

Alkoxylation of benzylic C(sp3 )-H bonds has become one of the most important tools for the construction of benzyl ethers from feedstock chemicals. Herein, we reported a silver catalyzed alkoxylation of benzylic C(sp3 )-H bonds employing potassium persulfate as an oxidant at room temperature. This strategy showed good functional-group tolerance, site selectivity, and chemoselectivity. The reaction proceeded smoothly in the presence of various primary, secondary, and tertiary alcohol nucleophiles, affording corresponding benzyl ethers. Combined experimental studies provided mechanistic insights into the possible radical pathways. Furthermore, a possible mechanism was proposed for this method.

Due to the consumers demand for quality wines, washing and disinfection operations are necessary in wine productions, leading to the generation of large volumes of winery wastewater (WW) with a high organic content which has the potential to cause irreversible environmental impacts. The aim and novelty of this work is the production of natural organic coagulants (NOCs) to be applied in coagulation-flocculation-decantation (CFD) process. To complement this treatment process, it is also aimed the performed a photo-Fenton process, combining hydrogen peroxide (H2O2) and potassium persulfate (KPS). The Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM) showed that NOCs are carbon-based materials with adsorption capacity. Under the best operational conditions, NOCs achieved a turbidity removal between 86.2 and 98.9%, a total suspended solids (TSS) removal ranging between 85.0 and 94.9% and a dissolved organic carbon (DOC) removal ranging between 14.1 and 44.9%. To degrade the DOC present in the WW, different advanced oxidation processes (AOPs) were tested. Results showed that KPS-photo-Fenton, under the best operational conditions [Fe2+] = 2.5 mM, [KPS] = 1.0 mM, pH = 3.0, radiation UV-C mercury lamp (254 nm), agitation 350 rpm, temperature 298 K, reaction time 240 min achieved a DOC removal of 91.2 and 96.8%, with a H2O2 consumption of 156.9 and 199.0 mM, respectively for red and white WW. With application of combined CFD-KPS-photo-Fenton process, it was observed an increase of DOC removal with lower H2O2 consumptions. The energy consumption of the photosystem was evaluated by application of electric energy per mass (EEM). The application of KPS-photo-Fenton process achieved an EEM of 0.308 and 0.0309 kWh/g/L DOC, with a cost of 2.05 and 2.59 €/g/L DOC respectively for red and white WW. The combination of CFD-KPS-photo-Fenton decreased significantly the costs of treatment and the treated wastewater achieved the Portuguese legal values for wastewater discharge. This work shows that NOCs are a promising technology that can be an alternative to traditional metal salts, the combination of sulfate radicals with hydroxyl radicals can achieve high DOC removal and the combination of CFD with KPS-photo-Fenton process can decrease the operational costs.

p-Phenylenediamine (p-PDA) is a monomer of many important polymers such as kevlar, twaron, poly-p-PDA. Most of the noticed polymers formation is initiated by a free-radical, but their polymerization mechanism is not elucidated computationally. The proposed study helps to fully understand the frequently utilized initiator/oxidant, potassium persulfate (K2 S2 O8 ) role in the aromatic diamines polymerization, which support experimental protocols, and a polymer scope. The formation of the poly-p-PDA is studied with the density functional theory (DFT) B3LYP-D3 functional using experimental polymerization parameters (0°C and aqueous media). K2 S2 O8 initiated free-radical polymerization of p-PDA is studied in detail, taking into account sulfate free-radical (SO4 - )· , SFR, persulfate anion (S2 O8 )2- , PA and K2 S2 O8 cluster, PP. The reaction mechanism is calculated as the conversion of p-PDA to free-radical, the p-PDA free-radical attack to the next p-PDA (dimerization), ammonia extrusion from the dimer adduct, the dimer adduct conversion to the free-radical (completion of p-PDA polymerization cycle) for the polymer chain elongation. Calculations show that the dimerization step is the rate-limiting step with a 29.2 kcal/mol energy barrier when SFR initiates polymerization. In contrast, the PA-assisted dimerization energy barrier is only 12.7 kcal/mol. PP supported polymerization is calculated to have very shallow energy barriers completing the polymerization cycle, i.e., dimerization (TS2K, ∆G‡  = 11.6 kcal/mol) and ammonia extrusion (TS3K, ∆G‡  = 6.7 kcal/mol).

Biomass-derived porous carbonaceous materials are efficient adsorbents for VOCs, but their traditional preparation method, pyrolysis combined with activation, suffers from high energy consumption, equipment corrosion, and low pore-making efficiency, which hinders their large-scale practical application. A novel method of alkali metal-catalyzed hydrothermal carbonization coupling with chemical activation for the preparation of microporous carbon is presented. Porous carbon with well-developed microporosity deriving from corn husk were prepared through the hydrothermal carbonization using potassium persulfate (K2S2O8) as a catalyst and programmed heating activation process. And the products were applied to removal of typical oxygen-containing VOCs, ethyl acetate. The addition of K2S2O8 in hydrothermal carbonization accelerated the biomass hydrolysis, decomposed the biopolymer, and formed functional hydrochars. Potassium salts introduced into the hydrochars, which acted as an activator in this programmed heating activation process, formed a great deal of micropores. The specific surface area of micropores increased by 81%, and the specific surface area of micropores less than 1 nm increased by 180%. The introduction of K2S2O8 in preparation improved the adsorption performance of CH-based porous carbons 16.46% and 60.00% respectively at different preparation temperatures (600 °C and 800 °C). Basing on these results, the improvement of micropores less than 1 nm is directly related to the adsorption performance. This indicates that pores (<1 nm) respond well to the adsorption of ethyl acetate.

Here in, a special catalytic system of potassium persulfate (K2S2O8, PS) activated by Bi2MoO6-CuS composite was established for the orange II (OII) degradation under visible light. The Bi2MoO6-CuS composite was synthesized by a two-step hydrothermal and solvothermal methods. The structure, morphology, light absorption and photocatalytic properties of the composite were respectively characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible diffuse reflectance spectroscopy (UV-vis DRS). The removal efficiency of OII degradation in the Bi2MoO6-CuS/PS/vis system reached to 98% within 80 min, which was much higher than that of either Bi2MoO6 or CuS alone. A feasible mechanism analysis of OII degradation was proposed and validated by simple classical quenching experiments and electron spin resonance (ESR) spectroscopy. The high removal efficiency by the nanocomposite could be attributed to highly active species of O2·-, ·OH and SO4•- radicals in the Bi2MoO6-CuS photocatalytic oxidation system. Moreover, the composite material retained its activation performance even after 5 degradation cycles, which suggested its high stability.