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Hydrothermal technology (HT) has received much attention in recent years as a process to convert wet organic waste into hydrochar. The aqueous phase (HTAP) produced by this process is still a burden and has become a bottleneck issue for HT process development. In this study, we provide the first investigation of the HTAP characteristics, phytotoxicity, and their correlation with persulfate (PS) (PS, 2.0 mmol/g TS)-assisted municipal sludge HT. The results showed that PS accelerated the hydrolysis of protein substances and increased the concentration of NH

Hydrothermal carbonization (HTC) is a promising carbon-neutral technology for converting sewage sludge (SS) and agricultural waste into energy. However, HTC-generated aqueous phase (AP) impedes the development of the former. This study investigated the potential of SS with rice husk (RH) and wheat straw (WS) co-HTC to form hydrochar and AP as substitutes for fuel and chemical fertilizer, respectively. Compared with single SS hydrochar, the yield of co-HTC-based hydrochar and higher heating value significantly increased by 10.9%-21.6% and 4.2%-182.7%, reaching a maximum of 72.6% and 14.7 MJ/kg, respectively. Co-HTC improves the safe handling, storage and transportation, and combustion performance of hydrochar. The total nitrogen concentration in AP-SS was 2575 mg/L, accounting for 67.7% of that found in SS. Co-HTC decreased and increased the amine and phenolic components of AP, respectively. AP-SS-RH and AP-SS-WS significantly increased pakchoi dry weight by 45.5% and 49.4%, respectively, compared with AP-SS. The results of the hydroponic experiments with AP instead of chemical fertilizers revealed that AP-SS did not reduce pakchoi dry weight by replacing20% chemical fertilizers. However, AP-SS-RH or AP-SS-WS replaced 60% chemical fertilizers. Therefore, the co-HTC of SS and agricultural waste increased the AP substitution of chemical fertilizer from 20% to 60%. These findings suggest that the co-HTC of agricultural waste with SS is a promising technology for converting SS into renewable resource products for fuels and N-rich liquid fertilizer while significantly improving fuel and fertilizer quality.

Microporous polymer membranes have received extensive attention in the membrane separation field based on the advantage of high gas permeance and low cost. However, there are a few reports of microporous polyacrylate membranes fabricated by interfacial polymerization (IP), and the formation mechanism and influence factor of the microporous structure is rarely illuminated. In this work, thin-film polyacrylate membrane with circular microporous morphology were prepared by IP method with cyclodextrin and acyl chloride as the aqueous and oil phase monomer respectively for effective gas separation. The effects of the aqueous and organic phase monomer structure and concentration, the concentration and type of alkali in the aqueous solution on the membrane morphology and gas separation performance were investigated in detail. As a result, the polyacrylate membrane fabricated by β-cyclodextrin (β-CD) and trimesoyl chloride (TMC) with optimal content of NaOH in the aqueous phase formed the special circular microporous structure by the scanning electronic microscope (SEM) characterization. The resulting membrane showed CO2 permeance of 200 GPU with CO2/N2 ideal separation selectivity of 10.53. This work provides an effective strategy to fabricate high performance polyacrylate membrane by regulating the monomer structure and the alkali concentration in the aqueous phenol solution with IP method, which would inspire the exploration of other phenolic monomer for the assembly of microporous polymer membranes for gas separation or seawater desalination.

Polymers of intrinsic microporosity (PIM) as one of potential next generation membrane materials for gas separation has attracted great interests due to its ultra-permeable characteristics. Herein, a novel bis(phenyl)fluorene-based PIMs (Cardo-PIM-1) based on 9,9-bis(3,4-dihydroxyphenyl) fluorene (BDPF), 2,3,5,6-tetrafluoroterephthalonitrile (TFTPN) and spirocyclic 5,5′,6,6′-tetrahydroxy-3,3′,3,3′-tetramethylspirobisindane (TTSBI) were prepared vis dibenzodioxane polymerization reaction, and then the functionalized multi-walled carbon nanotubes (f-MWCNTs) were incorporated into Cardo-PIM-1 to fabricate mixed matrix membranes (MMMs) with solution mixing method for CO2 separation. The structure analysis indicated that the MWCNTs were cut into short ropes and the amino groups were incorporated into the nanotubes surface after treated with acid mixtures followed by ethylenediamine modification. FTIR spectroscopy and nuclear magnetic resonance (NMR) measurement confirmed the formation of Cardo-PIM-1 macromolecule. BET and positron annihilation lifetime spectroscopy (PALS) analysis exhibited that Cardo-PIM-1 contained larger pore-size distribution and fractional free volume (FFV), and preferential CO2 adsorption capacity over N2 compared with that of PIM-1. This work investigated the structure of polymer as well as the effect of nanofillers in the gas separation performance. High CO2 permeability of 2.9 × 104 Barrer with a desirable CO2/N2 separation factor of 24.2 was achieved using the MMMs with 7.5 wt% f-MWCNTs loading, which were among the best performance for CO2 separation. The Cardo-PIM-1/f-MWCNTs MMMs will provide a promising alternative in industrial flue gas separation and CO2 capture process.