One-step synthesis of highly fluorescent carbon dots as fluorescence sensors for the parallel detection of cadmium and mercury ions.

Cadmium (Cd2+) and mercury ions (Hg2+) are essential for the quality control of food samples because of their serious toxicity to human health, but the effective and simple strategy for their parallel detection remains challenging. In this paper, a rapid and simple parallel detection method for Cd2+ and Hg2+ was developed using carbon dots (CDs) as fluorescent sensors. A one-step hydrothermal method with a single precursor l-arginine as both the carbon and nitrogen sources was employed to prepare nitrogen-doped CDs (N-CDs). N-CDs exhibited a uniform particle size and excitation-independent fluorescence emission. The maximum emission wavelength of N-CDs was observed at 354 nm with the excitation wavelength at 295 nm. The quantum yield of N-CDs reached as high as 71.6% in water. By using sodium diphosphate and phytic acid as masking agents, the fluorescent sensor can be quenched by Cd2+ and Hg2+ in the linear range of 0-26.8 µM and 0-49.9 µM within 5 min. Other common ions in farm products showed no significant effect on the fluorescence intensity of the sensing system. The results demonstrated that the sensing system had good selectivity and sensitivity for Cd2+ and Hg2+. The detection limits for Cd2+ and Hg2+ were 0.20 and 0.188 µM, respectively. In addition, the fluorescent sensor had been successfully applied for the detection of Cd2+ and Hg2+ in fruits and vegetables, and the recoveries were 86.44-109.40% and 86.62-115.32%, respectively. The proposed fluorescent sensor provides a rapid, simple, and sensitive detection method for Cd2+ and Hg2+ in food samples and thus a novel quantitative detection method for heavy metal ions in foods.

Fluorescent carbon dots from water hyacinth as detection sensors for ferric ions: the preparation and optimisation using response surface methodology.

The search for alternatives to chemicals from natural products as precursors for the preparation of highly doped carbon dots (CDs) remains challenging. Novel CDs (W-CDs) were synthesised using a one-step pyrolysis method with wastewater hyacinth as the sole carbon and nitrogen source at a mild temperature without using any surface-activating reagents or salt. The obtained W-CDs emitted strong blue fluorescence under 365 nm UV light excitation, with a quantum yield of 15.12%. The Box-Behnken design of the response surface methodology was applied to optimize the W-CD preparation conditions, including the reaction temperature, reaction time and weight of water hyacinths. The temperature was found to be the most important factor affecting the fluorescence intensity of the W-CDs. Additionally, the fluorescence sensor based on W-CDs demonstrated excellent selectivity towards ferric (Fe) ions, with a limit of detection of 2.35 µM. The fluorescent sensor was successfully applied for detecting Fe3+ in real water samples with a recovery of 97.80-103.10%. Hence, the pyrolysis of water hyacinth is proven to be a rapid, effective and green approach for CDs and provides a novel method for recycling water hyacinth.

Insights into the mechanism of hydrogen peroxide activation with biochar produced from anaerobically digested residues at different pyrolysis temperatures for the degradation of BTEXS.

The disposal of large amounts of biogas residue from anaerobically digested waste is a burden on environment protection. Porous biochars (BCs) were synthesized from biogas residue at three pyrolysis temperatures (300 °C, 550 °C, and 800 °C) and used to catalyze H2O2 for the degradation of benzene, toluene, ethylbenzene, xylene isomers (ortho, para, and meta), and styrene (BTEXS) to develop a new use for biogas residues. The prepared BCs were characterized through scanning electron microscopy, Brunauer-Emmett-Teller method, Fourier transform infrared spectrometry, and X-ray photoelectron spectroscopy. Results showed that BC800/H2O2 had the highest BTEXS degradation performance over 6 h. The degradation kinetic data were most consistent with the pseudo-second-order model. The different catalytic effect of the three BCs pyrolyzed at different temperatures were attributed to the dominant active sites (C-O/C-OH/C=C/C=O groups, pyridinic N, and graphitic N) that induced the production of reactive oxygen species (ROS). ROS-quenching experiments indicated that the degradation of BTEXS by BC300/H2O2, BC550/H2O2, and BC800/H2O2 involved ∙OH, ∙O2-, and 1O2. ∙OH was the dominant ROS in BC300/H2O2 and BC550/H2O2, and 1O2 was the dominant ROS in BC800/H2O2. Our findings provided new insight into the different catalytic mechanisms for BC production at different pyrolysis temperatures and demonstrated that a porous BC catalyst with high utilization value could be prepared from biogas residue and could hold considerable potential for application in BTEXS treatment in the future.

Degradation of BTEXS with stable and pH-insensitive iron-manganese modified biochar from post pyrolysis.

An efficient iron-manganese modified biochar (FMBC) was successfully synthesized as a heterogeneous Fenton-like catalyst through easy post-modification and applied for degradation of benzene, toluene, ethylbenzene, xylene isomers (ortho, para, and meta), and styrene (BTEXS) in the presence of H2O2. The catalyst was characterized by Brunauer-Emmett-Teller method, scanning electron microscopy, and X-ray photoelectron spectrometry. The effects of H2O2 concentration, FMBC dose, and initial pH on BTEXS degradation were also investigated. Results showed that degradation efficiency of FMBC for individual BTEXS varied from 83.05% to 94.12% in 3 h. Kinetic analysis showed that a first-order kinetic model with respect to BTEXS concentration could be used to explain the BTEXS degradation for FMBC/H2O2 system. The degradation reaction was more suitable in a wide pH range (3-10) than those in previous studies, thereby overcoming the low-efficiency problem of conventional Fenton reaction at high pH. Moreover, the doses of FMBC and H2O2 are a crucial factor affecting BTEXS degradation. Radical scavenger experiments revealed that ∙OH, ∙O2-, and 1O2 participated in the degradation process, and ∙OH was the major contributor. The synthesized catalyst is durable with stable BTEXS removal efficiency after seven consecutive cycles. The removal efficiency of BTEXS by FMBC in produced water reached 93.23% in 12 h, indicating FMBC has practical value.