A critical review of state-of-the-art electrocoagulation technique applied to COD-rich industrial wastewaters

Environmental Science and Pollution Research - Electrocoagulation (EC) is one of the emerging technologies in groundwater and wastewater treatment as it combines the benefits of coagulation,...     

Re-evaluating the asymmetric conventional energy and renewable energy consumption-economic growth nexus for Pakistan

Environmental Science and Pollution Research - To understand the nexus between economic growth and energy sources, in this study, we have selected Pakistan and collected data over the period...     

Mapping farmers’ vulnerability to climate change and its induced hazards: evidence from the rice-growing zones of Punjab,Pakistan

Environmental Science and Pollution Research - In developing countries like Pakistan, agriculture constitutes the primary source of support for the majority of rural and the adjacent urban...     

Photocatalytic degradation of crystal violet dye under sunlight by chitosan-encapsulated ternary metal selenide microspheres

Environmental Science and Pollution Research - Organic dyes that are extensively released in wastewater from various industries remain the priority concern in the modern world. Therefore, a novel...     

Watering techniques and zero-valent iron biochar pH effects on As and Cd concentrations in rice rhizosphere soils, tissues and yield

Zero-valent iron amended biochar (ZVIB) has been proposed as a promising material in immobilizing heavy metals in paddy fields. In this study, the impacts of pH of ZVIB (pH 6.3 and pH 9.7) and watering management techniques (watering amount in the order of CON (control, 5/72)>3/72>1–3/72>3/100>1/72, with 5/72, for example, representing irrigation given to 5 cm above soil surface in 72 hr regular interval) on As and Cd bioavailability for rice and its grain yield (Yield_BR) were investigated in a pot experiment. Brown rice As (As_BR) content was irrelative to the watering treatments, while significantly decreased (>50%) with the addition of both ZVIB materials. The diminutions of brown rice Cd (Cd_BR) content as well as the Yield_BR were highly dependent on both the soil amendment materials’ pH and watering amount. Among all the watering treatments, 3/72 treatment (15% less irrigation water than the CON) with ZVIB 6.3 amendment was the optimum fit for simultaneous reduction of As_BR (50%) and Cd_BR contents (19%) as well as for significant increment (12%) of the Yield_BR. Although high pH (9.7) ZVIB application could also efficiently decrease As and Cd contents in brown rice, it might risk grain yield lost if appropriate (e.g. 3/72 in our study) watering management technique was not chosen. Therefore, ZVIB would be an environmentally friendly option as an amendment material with proper selection of watering management technique to utilize As and Cd co-contaminated arable soils safely for paddy cultivation.     

Chemical characterization and source apportionment of PM1 and PM2.5 in Tianjin, China: Impacts of biomass burning and primary biogenic sources

The submicron particulate matter (PM₁) and fine particulate matter (PM_2.5) are very important due to their greater adverse impacts on the natural environment and human health. In this study, the daily PM₁ and PM_2.5 samples were collected during early summer 2018 at a sub-urban site in the urban-industrial port city of Tianjin, China. The collected samples were analyzed for the carbonaceous fractions, inorganic ions, elemental species, and specific marker sugar species. The chemical characterization of PM₁ and PM_2.5 was based on their concentrations, compositions, and characteristic ratios (PM₁/PM_2.5, AE/CE, NO₃^?/SO₄^2?, OC/EC, SOC/OC, OM/TCA, K+/EC, levoglucosan/K⁺, V/Cu, and V/Ni). The average concentrations of PM₁ and PM_2.5 were 32.4 µg/m³ and 53.3 µg/m³, and PM₁ constituted 63% of PM_2.5 on average. The source apportionment of PM₁ and PM_2.5 by positive matrix factorization (PMF) model indicated the main sources of secondary aerosols (25% and 34%), biomass burning (17% and 20%), traffic emission (20% and 14%), and coal combustion (17% and 14%). The biomass burning factor involved agricultural fertilization and waste incineration. The biomass burning and primary biogenic contributions were determined by specific marker sugar species. The anthropogenic sources (combustion, secondary particle formation, etc) contributed significantly to PM₁ and PM_2.5, and the natural sources were more evident in PM_2.5. This work significantly contributes to the chemical characterization and source apportionment of PM₁ and PM_2.5 in near-port cities influenced by the diverse sources.     

Elemental mercury (Hg0) removal from coal syngas using magnetic tea-biochar: Experimental and theoretical insights

Mercury is ranked 3^rd as a global pollutant because of its long persistence in the environment. Approximately 65% of its anthropogenic emission (Hg⁰) to the atmosphere is from coal-thermal power plants. Thus, the Hg⁰ emission control from coal-thermal power plants is inevitable. Therefore, multiple sorbent materials were synthesized using a one-step pyrolysis method to capture the Hg⁰ from simulated coal syngas. Results showed, the Hg⁰ removal performance of the sorbents increased by the citric acid/ultrasonic application. T5CUF_0.3 demonstrated the highest Hg⁰ capturing performance with an adsorption capacity of 106.81 µg/g within 60 min at 200 °C under complex simulated syngas mixture (20% CO, 20% H₂, 10 ppmV HCl, 6% H₂O, and 400 ppmV H₂S). The Hg⁰ removal mechanism was proposed, revealing that the chemisorption governs the Hg⁰ removal process. Besides, the active Hg⁰ removal performance is attributed to the high dispersion of valence Fe₃O₄ and lattice oxygen (α) contents over the T5CUF_0.3 surface. In addition, the temperature programmed desorption (TPD) and XPS analysis confirmed that H₂S/HCl gases generate active sites over the sorbent surface, facilitating high Hg⁰ adsorption from syngas. This work represented a facile and practical pathway for utilizing cheap and eco-friendly tea waste to control the Hg⁰ emission.     

Tissue distribution of 210Po and 210Pb in select marine species of the coast of Kudankulam, southern coast of Gulf of Mannar, India

Activities of ²¹⁰Po and ²¹⁰Pb in various tissues of four species of decapod crabs and two species of cephalopod mollusks (cuttlefishes) of Kudankulam coast were studied. A non-uniform distribution of these radionuclides was observed between the organs. Of all the tissues, ²¹⁰Po and ²¹⁰Pb were found accumulated more in the hepatopancreas and intestine of crabs and in the digestive gland, shell gland, and intestine of cephalopods. Among crabs, Charybdis lucifera registered a little higher ²¹⁰Po and ²¹⁰Pb activities. The cephalopod species Loligo duvauceli displayed higher ²¹⁰Po and ²¹⁰Pb in some organs when compared to Sepia pharaonis. The muscle of all the species registered lower activity. In cephalopods, the activity ratio of ²¹⁰Po/²¹⁰Pb fell within the range of 1?C2 for most of the organs, and in crab tissues, it varied from 1.7 to 31.4. The biological concentration factor for organs of cephalopods ranged from 1.2 ×10³ to 4.3 ×10⁵ for ²¹⁰Po and 4.8 ×10² to 8.4 ×10⁴ for ²¹⁰Pb and for organs of crabs it varied between 2.0 ×10⁴ and 1.9 ×10⁶ for ²¹⁰Po and 9.2 ×10² and 2.4 ×10⁴ for ²¹⁰Pb. The study revealed that the organs associated with digestion and metabolism displayed a higher activity concentration than the other tissues. A significant variation in the accumulation of ²¹⁰Po and ²¹⁰Pb was noted between species (P?<?0.05). The activity levels recorded are in agreement with values recorded in related organisms in other parts of the world. The data generated will act as a reference database for these organisms of this coast in which a nuclear power station is under construction.     

Determination of total and partially extractable solid-bound element concentrations using collision/reaction cell inductively coupled plasma-mass spectrometry and their significance in environmental studies

Determination of solid-bound element concentrations is an important initial step in environmental studies especially for assessment of contamination level, and of origin, relative mobility, and fate of contaminants. This study revealed that a relatively new collision/reaction cell inductively coupled plasma-mass spectrometry is a potent tool for determining total and partially extractable solid-bound element (V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, and Pb) concentrations in a complex matrix solution containing HF and/or HCl. Six different extraction methods commonly used for environmental monitoring studies were tested for their bias and variability using estuarine and marine standard reference materials. Microwave-assisted methods based on concentrated [HNO₃] or [HNO₃?+?HF (4:1)] and [HNO₃?+?HF?+?HCl (10:3:2)] were applied for determining pseudo-total and total element concentrations, respectively. Dilute-acids (1 M HNO₃, 1 M HCl, and 0.5 M HCl) were utilized in single-step partial extraction protocols. Except the 0.5 M HCl cold-extraction method which was performed at room temperature, other partial extraction protocols used microwave-digestion. This study demonstrated that the use of microwave-assisted methods in studies aimed at determining the non-residual, non-specific extractable fractions of elements in solid environmental samples may result in overestimation, and thus needs to be re-examined. We believe that the cold extraction method will play a significant role in future environmental monitoring studies. Nevertheless, results of the cold extraction method not accompanied with total element concentrations have limited value, as the amount of extraction may vary significantly with the nature (origin) of the elements, and with the types of the samples. Therefore, we suggest combining microwave-assisted total digestion and 0.5 M HCl cold-extraction methods as a relatively cost- and time-effective, environmentally sound screening procedure for routine environmental monitoring programs involving a large number of samples from diverse geological and anthropogenic settings.     

Explosibility of micron- and nano-size titanium powders

Explosibility of micron- and nano-titanium was determined and compared according to explosion severity and likelihood using standard dust explosion equipment. ASTM methods were followed using a Siwek 20-L explosion chamber, MIKE 3 apparatus and BAM oven. The explosibility parameters investigated for both size ranges of titanium include explosion severity (maximum explosion pressure (P_max) and size-normalized maximum rate of pressure rise (K_St)) and explosion likelihood (minimum explosible concentration (MEC), minimum ignition energy (MIE) and minimum ignition temperature (MIT)). Titanium particle sizes were ?100 mesh (<150 μm), ?325 mesh (<45 μm), ≤20 μm, 150 nm, 60–80 nm, and 40–60 nm. The results show a significant increase in explosion severity as the particle size decreases from ?100 mesh with an apparent plateau being reached at ?325 mesh and ≤20 μm. Micron-size explosion severity could not be compared with that for nano-titanium due to pre-ignition of the nano-powder in the 20-L chamber. The likelihood of an explosion increases significantly as the particle size decreases into the nano range. Nano-titanium is very sensitive and can self-ignite under the appropriate conditions. The explosive properties of the nano-titanium can be suppressed by adding nano-titanium dioxide to the dust mixture. Safety precautions and procedures for the nano-titanium are also discussed.