Worldwide there is an immense demand for plastic material that results in “white pollution”. Petrochemical-based plastic is used all over the world which leads to adverse impacts on every sphere of the earth. However, many steps have been taken to control this plastic pollution globally, such as chemical treatments, plastic waste incineration, sanitary landfilling, and 7 R programs. Still, plastic pollution is one of the major international problems. Non-biodegradable plastic would not eradicate from our environment until we have an economically feasible and more biodegradable substitute. In recent years algae, especially microalgae, have got attention worldwide, owing to their various applications. Microalgae is one of the sustainable ways of bioplastic synthesis as during cultivation it also purifies wastewater. This review paper has summarized various species of microalgae used for the synthesis of bioplastic, their cultivation system, and methods for bioplastic production by using microalgae biomass, followed by multiple challenges, solutions, and future prospects.

Pyrolysis is a promising thermochemical conversion process that transforms biomass into biochar, a carbon-rich solid material, in an oxygen-limited environment. This study focuses on the utilization of rice byproducts, namely rice straw and rice husk as feedstock for biochar production through low-temperature pyrolysis. The aim is to explore the potential of these biochars as cost-effective adsorbents for removing metal contaminants from aqueous solutions, with a particular emphasis on Pb(II) removal. Physicochemical properties of the biochars produced at a low temperature of 300 °C were thoroughly investigated, including surface morphology and their adsorption capacity for Pb(II). Remarkably, the rice straw biochar (RSB) produced at 300 °C exhibited exceptional Pb(II) adsorption capacity, with a value of 390.10±0.30 mg/g, and demonstrated a high Pb(II) removal efficiency of 96.10±0.30% when modified with 30% w/w H2O2. A crucial aspect of this study lies in the evaluation of the cost-effectiveness of the biochar production process, particularly when compared to commercially available adsorbents. By demonstrating the potential of rice byproduct-derived biochar as an efficient Pb(II) biosorbent in aqueous environments, this work not only provides new insights into the preparation of biochar using low-temperature pyrolysis but also offers a viable and economical solution for metal-contaminated water treatment. The findings of this research contribute to the field of sustainable waste utilization and highlight the significant potential of rice byproduct-based biochar as an environmentally friendly adsorbent for heavy metal removal.

The aim of this study is to synthesize and characterize an economical and environmentally-friendly adsorbent with high adsorption capacity. For this purpose, the walnut shells (Juglans regia L.) were chemically modified using sulfuric and citric acids, separately. After pyrolysis and synthesis of activated carbon (AC), the optimization of conditions at the preconcentration/removal step was performed using parameters such as pH and contact time for uranium in the model solutions. The measurements were carried out by inductively coupled plasma-mass spectrometry (ICP-MS). From the shapes of the BET isotherms, it may be stated that activated carbon exhibit type I. It was found that the surface area and total pore volume of the activated carbon were 696.6 m2/g and 0.35 mL/g, respectively. The adsorption capacity was found to be 220 mg/g. It was found that the optimum pH is 6.0 for preconcentration/removal using AC obtained by sulfuric acid as chemically-modifier. The optimized method was applied to determination of U at ng/mL levels in the model solutions.

This study analyzed the potential use of Mahagoni wood charcoal (MWC) and Mahagoni bark charcoal (MBC) as biosorbent for reactive red 120 (RR 120) dye removal from aqueous solutions. The effect of different operating parameters such as contact time (1–210 min), pH (3–11), adsorbent dose (1–20 g/L), and initial RR 120 concentration (5–70 mg/L) on adsorption processes was studied under batch adsorption experiments. The maximum removal of RR 120 by MWC (78%) and MBC (88%) was achieved when the optimum conditions were initial RR 120 concentration (5 mg/L), pH (3), adsorbents dose (10 g/L) and equilibrium contact time (150 min). The RR 120 adsorption data of MWC and MBC were better described by the Langmuir and Freundlich isotherm models, respectively. The MWC and MBC showed maximum adsorption capacities of 3.806 and 5.402 mg/g, respectively. Kinetic adsorption data of all adsorbents (MWC and MBC) followed the pseudo-second-order model and this adsorption process was controlled by chemisorption with multi-step diffusion. A lower desorption rate advocated that both strong and weak binding forces could exist between RR 120 molecules and adsorbents. The study results revealed that the utilization of either MWC and or MBC as an adsorbent for treating RR 120 is effective and environmentally friendly.

International audience

Filterable PM2.5 concentrations and their chemical characterizations were analyzed for 67 boilers and 25 indirect furnaces located in the Metropolitan Area of Costa Rica from February 2014 to November 2015. The PM2.5 samples were characterized by their composition, focusing on trace elements, inorganic ions and organic and elemental carbon. The results of PM2.5 concentrations ranged from 72 to 735 mgm-3, with the highest concentrations found for sources using biomass fuel, particularly Type B boilers, and the lowest values for diesel boilers. Further speciation of fine particulate matter (PM) showed significant levels of vanadium and nickel for boilers that use heavy fuel oil (bunker); 4886 and 1942 μgm-3, respectively. Copper and manganese were the most relevant metals for biomass burning sources, due to plant absorption from the soil. As for ion concentration, sulfate presented the highest concentrations for biomass boilers and furnaces, whereas chloride only presented the highest concentrations for furnaces. To complete the balance, organic and elemental carbon (OC and EC) analyses were made, in which biomass burning sources presented values five times higher than oil fuels. A Spearman's correlation analysis was made for the data set, revealing significant relationships between heavy metals, sulfate, and fine PM with respect to heavy fuel oil. For the biomass sources, the correlations pointed to K, Na, Mn and, in some cases, oxygen. | Se analizaron las concentraciones filtrables de PM2.5 y sus caracterizaciones químicas para 67 calderas y 25 hornos indirectos ubicados en el Área Metropolitana de Costa Rica desde febrero de 2014 hasta noviembre de 2015. Las muestras de PM2.5 se caracterizaron por su composición, centrándose en oligoelementos, iones inorgánicos y carbono orgánico y elemental. Los resultados de las concentraciones de PM2.5 variaron de 72 a 735 mgm-3, con las concentraciones más altas encontradas para fuentes que utilizan combustible de biomasa, particularmente calderas Tipo B, y el valores más bajos para calderas diesel. Una mayor especiación de partículas finas (PM) mostró una significativa niveles de vanadio y níquel para calderas que utilizan fuel oil pesado (bunker); 4886 y 1942 mgm-3, respectivamente. El cobre y el manganeso fueron los metales más relevantes para las fuentes de combustión de biomasa, debido a Absorción de plantas del suelo. En cuanto a la concentración de iones, el sulfato presentó las mayores concentraciones para calderas y hornos de biomasa, mientras que el cloruro solo presentó las concentraciones más altas para los hornos. Para completar el balance, se realizaron análisis de carbono orgánico y elemental (OC y EC), en los cuales las fuentes de combustión de biomasa presentaron valores cinco veces superiores a los combustibles derivados del petróleo. La correlación de Spearman. Se realizó un análisis para el conjunto de datos, revelando relaciones significativas entre metales pesados, sulfato y PM fino con respecto al fuelóleo pesado. Para las fuentes de biomasa, las correlaciones apuntaron a K, Na, Mn y, en algunos casos, oxígeno. | As concentrações filtráveis ​​de PM2,5 e suas caracterizações químicas foram analisadas para 67 caldeiras e 25 fornos indiretos localizados na Região Metropolitana da Costa Rica de fevereiro de 2014 a novembro de 2015. As amostras de PM2,5 foram caracterizadas por sua composição, com foco em oligoelementos, íons inorgânicos e carbono orgânico e elementar. Os resultados para as concentrações de PM2,5 variaram de 72 a 735 mgm-3, com as concentrações mais altas encontradas para fontes que usam combustível de biomassa, particularmente caldeiras Tipo B, e os valores mais baixos para caldeiras a diesel. A maior especiação de partículas finas (PM) mostrou níveis significativos de vanádio e níquel para caldeiras que usam óleo combustível pesado (bunker); 4886 e 1942 mgm-3, respectivamente. O cobre e o manganês foram os metais mais relevantes para as fontes de combustão da biomassa, devido à absorção das plantas do solo. Em relação à concentração de íons, o sulfato apresentou as maiores concentrações para caldeiras e fornos a biomassa, enquanto o cloreto apresentou as maiores concentrações apenas para os fornos. Para completar o balanço, foram realizadas análises de carbono orgânico e elementar (OC e EC), nas quais as fontes de combustão de biomassa apresentaram valores cinco vezes maiores que os combustíveis derivados do petróleo. A correlação de Spearman. Uma análise foi realizada para o conjunto de dados, revelando relações significativas entre metais pesados, sulfato e MP fino em relação ao óleo combustível pesado. Para fontes de biomassa, as correlações apontaram para K, Na, Mn e, em alguns casos, oxigênio. | Universidad Nacional, Costa Rica | Universidad Autónoma Metropolitana, México | Escuela de Ciencias Ambientales

Particulate matter from wood burning emissions (Cwₒₒd) was quantified at five locations in the United Kingdom (UK), comprising three rural and two urban sites between 2009 and 2021. The aethalometer method was used. Mean winter Cwₒₒd concentrations ranged from 0.26 μg m⁻³ (in rural Scotland) to 1.30 μg m⁻³ (London), which represented on average 4% (in rural environments) and 5% (urban) of PM₁₀ concentrations; and 8% of PM₂.₅. Concentrations were greatest in the evenings in winter months, with larger evening concentrations in the weekends at the urban sites. Random-forest (RF) machine learning regression models were used to reconstruct Cwₒₒd concentrations using both meteorological and temporal explanatory variables at each site. The partial dependency plots indicated that temperature and wind speed were the meteorological variables explaining the greatest variability in Cwₒₒd, with larger concentrations during cold and calm conditions. Peaks of Cwₒₒd concentrations took place during and after events that are celebrated with bonfires. These were Guy Fawkes events in the urban areas and on New Year's Day at the rural sites; the later probably related to long-range transport. Time series were built using the RF. Having removed weather influences, long-term trends of Cwₒₒd were estimated using the Theil Sen method. Trends for 2015–2021 were downward at three of the locations (London, Glasgow and rural Scotland), with rates ranging from −5.5% year⁻¹ to −2.5% year⁻¹. The replacement of old fireplaces with lower emission wood stoves might explain the decrease in Cwₒₒd especially at the urban sites The two rural sites in England observed positive trends for the same period but this was not statistically significant.

Inhalation of respirable silica particles can cause serious lung diseases (e.g., silicosis and lung cancer), and the toxicity of respirable silica is highly dependent on its crystal form. Common combustion processes such as coal and biomass burning can provide high temperature environments that may alter the crystal forms of silica and thus affect its toxic effects. Although crystalline silica (i.e., quartz, tridymite, and cristobalite) were widely found at different temperatures during the burning processes, the sources and crystal transformation pathways of silica in the burning processes are still not well understood. Here, we investigate the crystal transformation of silica in the coal and biomass combustion processes and clarify the detailed transformation pathways of silica for the first time. Specifically, in coal burning process, amorphous silica can transform into quartz and cristobalite starting at 1100 °C, and quartz transforms into cristobalite starting at 1200 °C; in biomass burning process, amorphous silica can transform into cristobalite starting at 800 °C, and cristobalite transforms into tridymite starting at 1000 °C. These transformation temperatures are significantly lower than those predicted by the classic theory due to possibly the catalysis of coexisting metal elements (e.g., aluminum, iron, and potassium). Our results not only enable a deeper understanding on the combustion-induced crystal transformation of silica, but also contribute to the mitigation of population exposure to respirable silica.