• Energy Research
• 2021-2025close
• CN close
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• University of North Texas close

This article is an editorial on the research topic Microbial C1 Metabolism and Biotechnology. This special topic presents studies focused on the fundamental aspects of C1 metabolism in diverse microbial systems with the ability to convert anthropogenic greenhouse gases into valuable products.

By means of the saturation shake-flask technique, the saturation solubility data of 3,3′-diaminodiphenyl sulfone in 14 monosolvents (n-propanol, N,N-dimethylformamide, methanol, ethanol, ethylene g...

Phosphonic acid functionalization of gellan gum and chitosan biopolymers was successfully performed. In the first step, the sorption was investigated using La(III) ions before testing for the recovery of rare earth elements (REEs) from pretreated industrial acidic leachate. The sorbent was characterized by Fourier-transform infrared (FTIR), scanning electron microscopy with energy dispersive X-ray analysis (SEM-EDX), thermogravimetric analysis (TGA), Brunauer–Emmett–Teller (BET), and pH of zero charge (pHPZC) determination. FTIR and EDX results show efficient grafting of phosphoryl groups. The sorption was determined for the crude materials before functionalization (PGEG) and after phosphorylation (TBP-PGEG). More efficient sorption was seen for phosphorylated sorbent than for the crude composite. The sorption capacity is 0.226 mmol La g−1 for the PGEG while the value is 0.78 mmol La g−1 for the TBP-PGEG. We infer that phosphonate groups participate in the sorption. The most effective sorption is at pH = 4. The kinetic behavior was described using pseudo first-order equations (PFORE), pseudo second-order equations (PSORE), and resistance to intraparticle diffusion (RIDE). The sorption isotherms can be better represented by Langmuir and Sips equations than by the Freundlich equation. The sorbent shows high stability performance during reuse cycles with a limit on the decrease in the sorption performances and stability in the desorption performances. We have thus developed a good tool for the recovery of REEs with a selectivity higher than that of the non-functionalized components.

Quantification of the trade-offs among greenhouse gas (GHG) emissions, yield, and farmers’ incomes is essential for proposing economic and environmental nitrogen (N) management strategies for optimizing agricultural production. A four-year (2017–2020) field experiment (including four treatments: basic N fertilizer treatment (BF), suitable utilization of fertilization (SU), emission reduction treatment (ER), and high fertilization (HF)) was conducted on maize (Zea mays L.) in the North China Plain. The Life Cycle Assessment (LCA) method was used in this study to quantify the GHG emissions and farmers’ incomes during the whole maize production process. The total GHG emissions of BF, SU, ER, and HF treatments in the process of maize production are 10,755.2, 12,908.7, 11,950.1, and 14,274.5 kg CO2-eq ha−1, respectively, of which the direct emissions account for 84.8%, 76.8%, 74.9%, and 71.0%, respectively. Adding inhibitors significantly reduced direct GHG emissions, and the N2O and CO2 emissions from the maize fields in the ER treatment decreased by 30.0% and 7.9% compared to those in the SU treatment. Insignificant differences in yield were found between the SU and ER treatments, indicating that adding fertilizer inhibitors did not affect farmers’ incomes while reducing GHG emissions. The yield for SU, ER, and HF treatments all significantly increased by 12.9–24.0%, 10.0–20.7%, and 2.1–17.4% compared to BF, respectively. In comparison with BF, both SU and ER significantly promoted agricultural net profit (ANP) by 16.6% and 12.2%, with mean ANP values of 3101.0 USD ha−1 and 2980.0 USD ha−1, respectively. Due to the high agricultural inputs, the ANP values in the HF treatment were 11.2%, 16.6%, and 12.4% lower than those in the SU treatment in 2018–2020. In conclusion, the combination of N fertilizer and inhibitors proved to be an environmentally friendly, high-profit, and low-emissions production technology while sustaining or even increasing maize yields in the North China Plain, which was conducive to achieving agricultural sustainability.

Abstract MEPCMs have drawn tremendous attention in TES fields. In this study, eutectic of CA and PA was encapsulated by PVC, and the novel MEPCM for TES applications was developed. Microcapsules were prepared by solvent evaporation method and examined using DSC, SEM, LPSA, FTIR, thermal cycling test and TGA. DSC results demonstrated that the phase change temperature of CA-PA eutectic decreased after microencapsulation. The most satisfied sample was the MEPCM with a shell-core ratio of 1:2, which melted at 17.1 °C with the latent heat of 92.1 J/g, the encapsulation ratio was 57.7%. SEM images and LPSA results showed that the prepared MEPCMs were consisted with micro-sized spheres. FTIR results confirmed that the PCM core was successfully encapsulated by the PVC shell, and no chemical reaction was found among the components. The prepared MEPCM showed an excellent thermal reliability after 500 times of thermal cycling. Microencapsulation enhanced the starting temperature of CA-PA eutectic thermal decomposition, and the novel MEPCM exhibited an excellent thermal stability at working temperature from TGA results. Consequently, MEPCM (1:2) was the optimal composition and had great potential for TES applications.