The complaints arising from the problem of odorants released by composting plants may impede the construction of new composting facilities, preclude the proper activity of existing facilities or even lead to their closure, with negative implications for waste management and local economy. Improving the knowledge on VOC emissions from composting processes is of particular importance since different VOCs imply different odour impacts. To this purpose, three different organic matrices were studied in this work: dewatered sewage sludge (M1), digested organic fraction of municipal solid waste (M2) and untreated food waste (M3). The three matrices were aerobically biodegraded in a bench-scale bioreactor simulating composting conditions. A homemade device sampled the process air from each treatment at defined time intervals. The samples were analysed for VOC detection. The information on the concentrations of the detected VOCs was combined with the VOC-specific odour thresholds to estimate the relative weight of each biodegraded matrix in terms of odour impact. When the odour formation was at its maximum, the waste gas from the composting of M3 showed a total odour concentration about 60 and 15,000 times higher than those resulting from the composting of M1 and M2, respectively. Ethyl isovalerate showed the highest contribution to the total odour concentration (>99%). Terpenes (α-pinene, β-pinene, p-cymene and limonene) were abundantly present in M2 and M3, while sulphides (dimethyl sulphide and dimethyl disulphide) were the dominant components of M1.

In indoor air, terpene-ozone reactions can form secondary organic aerosols (SOA) in a transient process. ‘Real world’ measurements conducted in a furnished room without air conditioning were modelled involving the indoor background of airborne particulate matter, outdoor ozone infiltrated by natural ventilation, repeated transient limonene evaporations, and different subsequent ventilation regimes. For the given setup, we disentangled the development of nucleated, coagulated, and condensed SOA fractions in the indoor air and calculated the time dependence of the aerosol mass fraction (AMF) by means of a process model. The AMF varied significantly between 0.3 and 5.0 and was influenced by the ozone limonene ratio and the background particles which existed prior to SOA formation. Both influencing factors determine whether nucleation or adsorption processes are preferred; condensation is strongly intensified by particulate background. The results provide evidence that SOA levels in natural indoor environments can surpass those known from chamber measurements. An indicator for the SOA forming potential of limonene was found to be limona ketone. Multiplying its concentration (in μg/m³) by 450(±100) provides an estimate of the concentration of the reacted limonene. This can be used to detect a high particle formation potential due to limonene pollution, e.g. in epidemiological studies considering adverse health effects of indoor air pollutants.

Emission of BVOC (Biogenic Volatile Organic Compounds) from plant leaves in response to ozone exposure (O3) and nitrogen (N) fertilization is poorly understood. For the first time, BVOC emissions were explored in a forest tree species (silver birch, Betula pendula) exposed for two years to realistic levels of O3 (35, 48 and 69 ppb as daylight average) and N (10, 30 and 70 kg ha−1 yr−1, applied weekly to the soil as ammonium nitrate). The main BVOCs emitted were: α-pinene, β-pinene, limonene, ocimene, (E)-4,8-dimethyl-1,3,7-nonatriene (DMNT) and hexanal. Ozone exposure increased BVOC emission and reduced total leaf area. The effect on emission was stronger when a short-term O3 metric (concentrations at the time of sampling) rather than a long-term one (AOT40) was used. The effect of O3 on total leaf area was not able to compensate for the stimulation of emission, so that responses to O3 at leaf and whole-plant level were similar. Nitrogen fertilization increased total leaf area, decreased α-pinene and β-pinene emission, and increased ocimene, hexanal and DMNT emission. The increase of leaf area changed the significance of the emission response to N fertilization for most compounds. Nitrogen fertilization mitigated the effects of O3 exposure on total leaf area, while the combined effects of O3 exposure and N fertilization on BVOC emission were additive and not synergistic. In conclusion, O3 exposure and N fertilization have the potential to affect global BVOC via direct effects on plant emission rates and changes in leaf area.

Two primary schools and one kindergarten were selected in the city of Kozani, Greece in order to investigate the school environment, the indoor air pollutants that children are exposed to and possible health risks at school. In each school three classrooms and one outdoor position were monitored from Monday to Friday, in both non-heating (26/09/2011–14/10/2011) and heating (23/01/2012–10/02/2012) period. Temperature, relative humidity and CO2, were continuously monitored. Formaldehyde, benzene, trichloroethylene, pinene, limonene, NO2 and O3 were measured with diffusive samplers. CO was monitored every day (30 min/day). Radon was measured for four weeks with short term radon detectors. PM2.5 was gravimetrically determined while PM2.5 and PM10 fractions were measured using the optical light scattering technique. Building material emission testing for VOCs was performed using the Field and Laboratory Emission Cell (FLEC). The ventilation rate for each classroom was calculated based on the CO2 measurements.Results indicated that indoor air concentrations of the measured pollutants were within accepted limits with indicative ranges 1.5–9.4 μg/m3 for benzene, 2.3–28.5 μg/m3 for formaldehyde, 4.6–43 μg/m3 for NO2 and 0.1–15.6 μg/m3 for O3. Emissions from building materials seem to have a significant contribution to the indoor air quality. Very low ventilation rates (0.1–3.7 L/s per person) were observed, indicating inadequate ventilation and possible indoor air quality problems requiring intervention measures. The estimated average lifetime cancer risks for benzene, formaldehyde and trichloroethylene were very low.

The UK may be required to expand its bioenergy production in order to make a significant contribution towards the delivery of its ‘net zero’ greenhouse gas emissions target by 2050. However, some trees grown for bioenergy are emitters of volatile organic compounds (VOCs), including isoprene and terpenes, precursors in the formation of tropospheric ozone, an atmospheric pollutant, which require assessment to understand any consequent impacts on air quality. In this initial scoping study, VOC emission rates were quantified under UK climate conditions for the first time from four species of eucalypts suitable for growing as short-rotation forest for bioenergy. An additional previously characterised eucalypt species was included for comparison. Measurements were undertaken using a dynamic chamber sampling system on 2-3 year-old trees grown under ambient conditions. Average emission rates for isoprene, normalised to 30 °C and 1000 μmol m⁻² s⁻¹ PAR, ranged between 1.3 μg C gdw⁻¹ h⁻¹ to 10 μg C gdw⁻¹ h⁻¹. All the eucalypt species measured were categorised as ‘medium’ isoprene emitters (1–10 μg C gdw⁻¹ h⁻¹). Total normalised monoterpene emission rates were of similar order of magnitude to isoprene or approximately one order of magnitude lower. The composition of the monoterpene emissions differed between the species and major compounds included eucalyptol, α-pinene, limonene and β-cis-ocimene. The emission rates presented here contribute the first data for further studies to quantify the potential impact on UK atmospheric composition, if there were widespread planting of eucalypts in the UK for bioenergy purposes.

The present study explores the efficient management of non-degradable polystyrene foam wastes (PSFW) by transforming into a microbial responsive material for an effective biodegradation process. In brief, the study involves three steps, viz., (i) preparation of citrus fruit peel extract from peel wastes; (ii) dissolution of PSFW using the extract and transform to polystyrene sheet (PSS) and characterization of the sheet formed and (iii) finally the microbial adhesion and biofilm formation on PSS. Results revealed that the maximum yield of the peel extract identified as D-limonene was obtained from Citrus sinensis (8.2 ± 0.06 ml/100 g fresh waste). Characterization studies on PSS suggested that there are appreciable changes in the infrared spectrum, thermo gravimetric analysis, gel permeation chromatography analyses, and contact angle measurements in comparison with PSFW. Observations on significant variations in the glass transition temperature of PSFW (100 °C) and PSS (60 °C); decomposition temperature of PSFW (310.93 °C) and PSS (78.18 °C), and molecular weight distribution changes in PSFW (2.00 Mw/Mn) and PSS (1.03 Mw/Mn) suggested the occurrence of structural and molecular changes in PSS. Studies on microbial adhesion and biofilm formation on PSS suggested that amongst six microbial species isolated from the waste dump yard, WD03 strain identified as Lysinibacillus sp., displayed a maximum adhesion and biofilm formation on the surface of the PSS as evidenced through biofilm characterizations, SEM, and fluorescence microscopic analyses respectively. In conclusion, the transformation of PSFW to PSS and the appreciable microbial adhesion and biofilm formation suggested the possibility of the effective management of white nuisance (PSFW) wastes in the environment.

The Lippia alba essential oil (EO) is a fish anesthetic immiscible in water and commonly used diluted in ethanol. We evaluated the effectiveness of surfactant use with Lippia alba EO in the anesthesia of Oreochromis niloticus, as well as its toxicity in fish and mammals. The EO was extracted by hydrodistillation and the fish were exposed to anesthesia at the concentration of 250 μL/L for 10 min with the surfactants polysorbate 20 (T20), polysorbate 80 (T80), polyethylene glycol (PEG), and ethanol. We also evaluated fish recovery and anesthetic safety margin after exposure for 10, 20, and 30 min. To assess the surfactants’ toxicity in mammals, Mus musculus (mice) received the same treatments by gavage. The main constituents of the Lippia alba EO were linalool (42.36%), geraniol (12.46%), neral (10.7%), and limonene (7.45%). Deeper anesthesia was faster in the T20 (60 ± 2.9 s) and T80 (272 ± 21 s) treatment groups, while recovery time for T80 was longer (596 ± 47 s). All treatments showed a good safety margin, without mortality. The genotoxic effects caused by surfactants in mammals and fish were at similar levels to those found in the ethanol treatment. Therefore, this study demonstrated that the use of surfactants T20 and T80 in Oreochromis niloticus anesthesia presented neither a reduction nor a considerable increase of the toxicity when compared to the commonly used ethanol; however, an increase in anesthetic effectiveness was observed throughout the experiment.

Combining bioassays and analytical chemistry screenings is a powerful approach to assess emerging organic micropollutants which are the main contributors to toxic potentials in complex mixtures of water matrices. The aim of this study was to assess the cytotoxic effect of the occurrence of emerging organic micropollutants discharged into river water through industrial wastewater and treated effluents. The cytotoxic effects of surface water, treated effluents, and industrial wastewater were assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. Then, organic micropollutants of various chemical groups were identified using a detailed non-target screening based on gas chromatography coupled with a mass spectrometry detector (GC/MS). A significant cytotoxic effect on human intestinal epithelial Caco-2 cells was observed for all the samples. Caco-2 cell viability decreased by 17.99, 33.77, and 24.54 % for surface water, treated wastewater, and industrial water, respectively. The organic chemical compounds responsible for this toxic potential were identified using non-target chemical screening. Statistical correlation between cytotoxicity and the presence of emerging contaminants revealed that the cytotoxic effect was mainly due (r ≥ 0.42) to the occurrence of cyclopentasiloxane, decamethyl and cyclohexasiloxane, dodecamethyl, D-limonene, and ergoline-8-methanol, 8,9-didehydro-6-methyl while cytotoxicity was highly negatively correlated (r ≤ −0.42) to 2-ethylhexyl salicylate, 3-isopropoxy-1,1,1,7,7,7-hexamethyl-3,5,5-tris(trimethyl siloxy)tetrasiloxane, 6-acetyl-1,1,2,4,4,7-hexamethyltetralin, and (3-aminopropyltriethoxysilane. Seventy-six other compounds detected by GC/MS showed no correlation to cytotoxicity.

Most studies have shown that improper disposal of e-waste can accelerate the release of high concentrations of polybrominated diphenyl ethers (PBDEs), and this situation causes environmental pollution and human health risks. The recycling technology of waste electronic plastics based on solvent processes can reduce environmental pollution and health risks from PBDEs. In this study, high impact polystyrene (HIPS) from waste TV sets was taken as the research object, and d-limonene and n-propanol were used as solvent and precipitant, respectively. We studied the relationship between the precipitation conditions and the size of precipitate particles, and the effect laws of precipitation conditions on the removal percentage of PBDEs were discussed. Transferring behavior of PBDEs during precipitation was investigated, and the parameters suitable for removing PBDEs from HIPS solution were confirmed. Results showed that lower HIPS concentration in d-limonene, lower precipitation temperature, higher mass ratio of n-propanol to HIPS solution, and greater stirring speed were conducive to form smaller and more uniform precipitate particles. All conditions (concentration, temperature, mass ratio, and stirring rate) that could increase the solubility of PBDEs in the mixed solvent of limonene and n-propanol or decrease the swelling degree of HIPS precipitate particles, or reduce the size of particles could improve the removal percentage of PBDEs. The investigated results indicated that insoluble PBDEs (e.g., decabromodiphenyl ether) transferred into the HIPS precipitate mainly through the generated crystals and then precipitated together with the HIPS particles, and soluble PBDEs (e.g., octabromodiphenyl ether) migrated into the precipitate by the solution entrained. The precipitate particles, which measured approximately 1.0 mm (on average), were obtained when the solution containing 10% of HIPS from waste TV shell was precipitated by adding n-propanol equivalent to twice the mass of the solution at 40 °C and 3000 r/min stirring speed. The total concentration of PBDEs in the precipitate particles (dried) was reduced to 2369 mg/kg, and 88.06% of the PBDEs in the original plastic solution was successfully removed by this process.

Regional estimates of VOC fluxes focus largely on emissions from the canopy and omit potential contributions from the forest floor including soil, litter and understorey vegetation. Here, we measured monoterpene emissions every 2 months over 2 years from logged tropical forest and oil palm plantation floor in Malaysian Borneo using static flux chambers. The main emitted monoterpenes were α-pinene, β-pinene and d-limonene. The amount of litter present was the strongest indicator for higher monoterpene fluxes. Mean α-pinene fluxes were around 2.5–3.5 μg C m⁻² h⁻¹ from the forest floor with occasional fluxes exceeding 100 μg C m⁻² h⁻¹. Fluxes from the oil palm plantation, where hardly any litter was present, were lower (on average 0.5–2.9 μg C m⁻² h⁻¹) and only higher when litter was present. All other measured monoterpenes were emitted at lower rates. No seasonal trends could be identified for all monoterpenes and mean fluxes from both forest and plantation floor were ~ 100 times smaller than canopy emission rates reported in the literature. Occasional spikes of higher emissions from the forest floor, however, warrant further investigation in terms of underlying processes and their contribution to regional scale atmospheric fluxes.