To investigate the chemical composition, size distribution, and mixing state of aerosol particles on heavy pollution days, single-particle aerosol mass spectrometry was conducted during 9–26 October 2015 in Xi’an, China. The measured particles were classified into six major categories: biomass burning (BB) particles, K-secondary particles, elemental carbon (EC)–related particles, metal-containing particles, dust, and organic carbon (OC) particles. BB and EC-related particles were the dominant types during the study period and mainly originated from biomass burning, vehicle emissions, and coal combustion. According to the ambient air quality index, two typical episodes were defined: clean days (CDs) and polluted days (PDs). Accumulation of BB particles and EC-related particles was the main reason for the pollution in Xi’an. Most types of particle size were larger on PDs than CDs. Each particle type was mixed with secondary species to different degrees on CDs and PDs, indicating that atmospheric aging occurred. The mixing state results demonstrated that the primary tracers were oxidized or vanished and that the amount of secondary species was increased on PDs. This study provides valuable information and a dataset to help control air pollution in the urban areas of Xi’an. Graphical abstract

Discharge of unprocessed coloured waste water from industries gives rise to water contamination. In the current work, we propose the application of CuO nanoparticles supported on cellulose kitchen wipe sponge as a heterogeneous catalyst for the reductive decolourization of various toxic cationic and anionic dye molecules. The catalytic activity of the CuO nanoparticles under normal light for reduction has been examined in which sunlight irradiation is not necessitated. The CuO nanoparticles were synthesized by a simple wet chemical method and characterized using High Resolution Transmission Electron Microscope (HRTEM), SEM, EDX, XRD, XPS and TGA analyses. In the presence of CuO@CS catalyst and sodium borohydride, decolourization reaction of dyes such as acid red, acid green, methylene blue, rhodamine B and solochrome black-T was carried out. The catalytic reduction behaves as a pseudo-first-order reaction and is found to be superior in comparison with other reported catalysts in terms of reaction velocity. The reduction reaction can be further accelerated by increasing the reaction temperature. The developed catalyst drives the reduction faster on exposing the reaction mixture to sunlight confirming the usage of the catalyst at normal light and sunlight conditions. The catalyst retains 100% efficiency even after 5 cycles and remains suitable even for further use. Thus, a low-cost heterogeneous catalyst has been successfully developed and employed to decolourize various dye molecules in short duration with good recyclability and therefore can be used as the potential candidate in environmental remediation.

At present, diminishing oil resources and increasing environmental concerns have led to a shift toward the production of alternative biofuels. In the last few decades, butanol, as liquid biofuel, has received considerable research attention due to its advantages over ethanol. Several studies have focused on the production of butanol through the fermentation from raw renewable biomass, such as lignocellulosic materials. However, the low concentration and productivity of butanol production and the price of raw materials are limitations for butanol fermentation. Moreover, these limitations are the main causes of industrial decline in butanol production. This study reviews butanol fermentation, including the metabolism and characteristics of acetone-butanol-ethanol (ABE) producing clostridia. Furthermore, types of butanol production from biomass feedstock are detailed in this study. Specifically, this study introduces the recent progress on the efficient butanol production of “designed” and modified biomass. Additionally, the recent advances in the butanol fermentation process, such as multistage continuous fermentation, metabolic flow change of the electron carrier supplement, continuous fermentation with immobilization and recycling of cell, and the recent technical separation of the products from the fermentation broth, are described in this study.

Cadmium (Cd) contamination in soil has become the focus of widespread concern in society today. In this paper, with Eisenia fetida as research subjects, an indoor simulation experiment was conducted. A BIOLOG microplate technique was used to determine the carbon source (single-carbon) utilization of the microbial communities in the contaminated soil and earthworms under Cd stress. Contour line analysis was used for the first time to study the difference of carbon source metabolism in microbial communities. And the effects of Cd stress on the functional diversity of the microbial communities and the detoxification mechanism in earthworms were researched. With two test groups, a short-term test and the long-term test were performed. The former test lasted for 10 days, with the removal of an earthworm every day for analysis; the latter test lasted for 30 days, with the removal of an earthworm every 10 days. The Cd²⁺ concentration was set at 0, 50, 100, 125, 250, or 500 mg kg⁻¹ dry weight, and 10 earthworms were inoculated in each concentration treatment. The earthworm homogenate and soil extracts were used to determine the carbon source utilization of the microbial communities. The results show that Cd stress changed the functional diversity of the microbial communities in the soil and earthworms. With the extension of stress time and the increase of stress concentration, earthworms will adjust their own physiological functions (including the microbial community structure and stress mechanism in the body) and regulate the microbial community structure in the external environment to obtain the necessary substances for growth. In addition, 2-hydroxybenzoic acid, γ-hydroxybutyric acid, glutamyl-L-glutamic acid, α-butyric acid, threonine, and α-cyclodextrin were important carbon sources for the earthworms to maintain their normal physiological metabolism under Cd stress. This study confirms that changes in microbial communities can be used to reveal the detoxification mechanisms of earthworm under heavy metal stress.

Fe/activated coke (AC) and Cr-Fe/AC catalysts with AC as a supporter and Cr and Fe as active components were prepared by an impregnation method for low-temperature selective catalytic reduction (SCR) of NO with NH₃. The effects of Cr addition and its concentrations on the deNOₓ performance of Fe/AC catalysts were studied at low temperature. The Cr addition promotes the low-temperature SCR activity of the 8Fe/AC catalyst and the 8Fe6Cr/AC catalyst has the best low-temperature SCR deNOₓ performance, which the NOₓ conversions are greater than 90% at 160–240 °C. The 8Fe6Cr/AC catalyst has good water resistance. However, when 100 ppm SO₂ was introduced into the reaction gas, its deNOₓ efficiency drops to 45% at 180 °C. To clarify the specific effects of Cr addition on the NOₓ conversions and sulfur poisoning, the Cr-Fe/AC catalysts were characterized by X-ray diffraction, BET, H₂ temperature-programmed reduction, NH₃ temperature-programmed desorption, X-ray photoelectron spectroscopy, and Fourier infrared spectroscopy. The addition of Cr into Fe/AC catalysts greatly increases the BET surface area and the number of weak and medium-strong acid sites on the catalyst surface and improves the ratio of Fe³⁺/Fe²⁺. These factors enhance the NOₓ conversion of 8Fe/AC catalyst. The formed sulfates and hydrogen sulfates cover the active sites on the catalyst surface, which lead to the sulfur poisoning of the 8Fe6Cr/AC catalyst. Graphical abstract

Polyvinyl alcohol (PVA) filled with different kinds of ZnO whisker was prepared by chemical cross-linking reaction. It was found that the ZnO whiskers dispersed uniformly after being modified by 3-aminopropyltriethoxysilane (APTES). The PVA/tetrapod-shaped ZnO (PVA/tetra-ZnO) composites showed better adsorption performance than other kinds of PVA/ZnO composites. The framework-supported pore-channel structure was beneficial for the transmission and adsorption of heavy metal ions, and the formation of “brush” pore-channel of PVA/tetra-ZnO composites can effectively retain and capture the heavy metal ions. The PVA/tetra-ZnO composites presented well adsorption on Pb(II), Cd(II), and Cr(III) ions than Ni(II) and showed relatively selective removal on Pb(II) and Cr(III) ions. The adsorbed heavy metal ions presented gradient distribution with high content in the out layer and low content in the inner layer. Pb(II) adsorption capacity qₑ increased gradually with the increase of initial solution concentration and contact time which tended to be stable at 400 mg/L and 800 min. The maximal adsorption capacity qₘ obtained by nonlinear fitting reached to about 116 mg/g which was very close to the experiment data. Adsorption isotherm results indicated the monolayer adsorption process of the Langmuir model and the adsorption kinetics data fitted well to the pseudo-second-order model. The adsorption process was spontaneous and the high temperature was in favor of adsorption. The adsorption mechanism was explored as the combination of coordination and ion exchange. Besides, the PVA/tetra-ZnO composites exhibited better stress stability, thermo stability, and favorable regeneration than neat PVA.

Hydrothermal carbonisation (HTC) is a wet and relatively low-temperature process where, under autogenous pressures, biomass undergoes a chain of reactions leading to the defragmentation of organic matter. As well as its other uses (e.g. for producing low-cost carbon-based nano-compounds), HTC is utilised for the treatment of wet wastes, such as manure and biosludge. This study aimed to determine if hydrothermal carbonisation is a feasible treatment method for spent sorbents that are highly enriched with arsenic, chromium, copper, and zinc. The chemical properties of hydrochar and process liquid were evaluated after HTC treatment, where peat-based spent sorbents were carbonised at 230 °C for 3 h. Analysis of Fourier transform-infrared spectra revealed that during HTC, the oxygenated bonds of ethers, esters, and carboxylic groups were cleaved, and low-molecular-weight organic fragments were dissolved in the process liquid. A large fraction of arsenic (up to 62%), copper (up to 25%), and zinc (up to 36%) were transferred from the solids into the process water. Leaching of these elements from the hydrochars increased significantly in comparison with the spent sorbents.

The inspiration for this study was the anxiety of Warsaw beekeepers, who raised the question whether location of hives in large urban agglomerations results in changes in concentrations of xenobiotics, toxic elements, and micronutrients in honey bees. Preliminary studies required elaboration of the research methodology, as the studied object is characterized by a low degree of homogeneity and the method of sample preparation affects obtained results. From many tested approaches, the use of washed and milled abdomens of the bees is recommended. Results obtained for such prepared samples are slightly lower than for whole bees, but their repeatability is higher, which enables easier interpretation of the trends and comparison of different locations. The contents of selected elements (As, Al, Cd, Co, Cr, Cu, Mn, Pb, and Zn) were compared in bees from urban and rural areas. The studies were supported by pesticides analysis. Also, it was checked whether these substances are accumulated on the surface or inside the bee’s body. The research indicates the markers of contamination: Al, As, and Cr on the surface and Cd inside the bodies of honey bees. The location of the hives does not influence significantly the content of “toxic,” nutrient metals and metalloids in bees (slightly higher levels of As, Al, Pb, and Cd were found in bees from urban areas). In terms of exposure to these elements and pesticides, the large city environment is not harmful for honey bees.

This study evaluated an enhancement of simultaneous polycyclic aromatic hydrocarbon (PAH) biodegradation and lipid accumulation by Rhodococcus opacus using biochar derived cheaply from biomass gasification effluent. The chemical, physical, morphological, thermal, and magnetic properties of the cheaply derived biochar were initially characterized employing different techniques, which indicated that the material is easy to separate, recover, and reuse for further application. Batch experiments were carried out to study biochar-aided PAH biodegradation by R. opacus clearly demonstrating its positive effect on PAH biodegradation and lipid accumulation by the bacterium utilizing the synthetic media containing 2-, 3- or 4-ring PAH compounds, at an initial concentration in the range 50–200 mg L⁻¹, along with 10% (w/v) inoculum. An enhancement in PAH biodegradation from 79.6 to 92.3%, 76.1 to 90.5%, 74.1 to 88.2%, and 71.6 to 82.3% for naphthalene, anthracene, phenanthrene, and fluoranthene, respectively, were attained with a corresponding lipid accumulation of 68.1%, 74.2%, 72.4%, and 63% (w/w) of cell dry weight (CDW). From contact angle measurements carried out in the study, enhancement in PAH biodegradation and lipid accumulation due to the biochar was attributed to an improved bioavailability of PAH to the degrading bacterium.

Fluoroquinolones (FQs) occur broadly in natural media due to its extensive use, and it has systematic effects on our ecosystem and human immunity. In this study, long-root Eichhornia crassipes was reclaimed as a multi-functional activated carbon (MFAC) to remove fluoroquinolones (FQs) from contaminated water. To get insight into the adsorption mechanism, multiple measurements, including FTIR and XPS analyses, were employed to investigate the adsorption processes of ciprofloxacin and norfloxacin as well as the experiments of effect of exogenous factors on adsorption performances. The results confirmed that the adsorption of FQs by MFAC was mainly attributed to the electrostatic interaction, hydrogen bond interaction, and electronic-donor-acceptor (EDA) interaction. In addition, the kinetics and thermodynamics experiments demonstrated that the MFAC possessed great adsorption performance for FQs. According to the Langmuir model, the saturated adsorption capacities exceeded 145.0 mg/g and 135.1 mg/g for CIP and NOR at 303.15 K, respectively. The column experiments were conducted to explore the application performance of MFAC on the advanced treatment of synthetic water at different flow rates and bed depths. The adsorption capacity of CIP on MFAC was estimated by the Thomas models and the bed-depth service time (BDST) models, reaching 127.56 mg/g and 11,999.52 mg/L, respectively. These results also provide a valid approach for the resource recycling of the redundant long-root Eichhornia crassipes plants. Graphical abstract