Enhancing dissolved inorganic phosphorous capture by gypsum-incorporated biochar: Synergic performance and mechanisms.

Excess nutrients, such as phosphorus (P), in watersheds jeopardize water quality and trigger harmful algal blooms. Using phosphorus sorption material (PSM) to capture P from wastewater and agricultural runoff can help recover nutrients and prevent their water pollution. In this study, a novel designer biochar was generated by pyrolyzing woody biomass pretreated with a flue gas desulfurization gypsum. The removal of dissolved inorganic phosphorus (DIP) by the gypsum-incorporated designer biochar was more efficient than the gypsum, suggesting the pretreatment of biomass with the gypsum results in a synergic effect on enhancing DIP capture. The maximum P adsorption capacity of the designer biochar was more than 200 mg g-1 , which is one order of magnitude greater than that of the gypsum. This result clearly showed that the designer biochar is a better PSM to capture DIP from nutrient-contaminated water compared to the gypsum. Post-sorption characterization indicated that the sorption of DIP by the gypsum-incorporated biochar involves multiple mechanisms. The precipitation reactions of calcium (Ca) cations and P anions to form CaHPO4 and Ca3 (PO4 )2 precipitates on the highly alkaline surface of the designer biochar were identified as a main mechanism. By contrast, CaHPO4 ·2H2 O is the only precipitated product for DIP sorption by the gypsum. In addition, the initial solution pH and the coexisting bicarbonate had less effects on the DIP removal by the designer biochar in comparison with the gypsum, which further confirms that the former is an excellent PSM to capture DIP from a variety of aquatic media.

Influence of biosolids and sewage effluent application on sitagliptin soil sorption.

Biosolids and sewage effluent application to agricultural fields is becoming a win-win practice as both an economical waste management strategy and a source of nutrients and organic matter for plant growth. However, these organic wastes contain a variety of trace chemicals of environmental concern such as pharmaceuticals and personal care products (PPCPs), which may pose a risk to agricultural fields and ecosystems. This work aims to investigate the sorption of sitagliptin on four agricultural soils, evaluate the effects of biosolids and sewage effluent application, and elucidate the main sorption mechanism of the pharmaceutical on soils. The sorption study revealed that the sorption capacities of sitagliptin on different soils were positively related to the contents of soil organic matter and negatively associated with soil pH values. The application of biosolids and sewage effluent decreased the sorption capacity of sitagliptin, which may be attributed to the loading of dissolved organic matter derived from organic wastes. The Freundlich isotherm model demonstrated that the addition of biosolids from 0 to 100 % (W/W) consistently decreased the sorption affinity (Kf) of sitagliptin from 1.69 × 102 to 3.82 × 101 mg(1-n) Ln kg-1. Sewage application at 0, 10, 50, and 100 % (V/V) also reduced the Kf values from 1.69 × 102 to 9.17 × 101 mg(1-n) Ln kg-1. Attenuated Total Reflection (ATR)-Infrared (IR) spectroscopy analyses suggested that electrostatic interactions between carbonyl and amino groups of sitagliptin and the negatively charged soil surface are the main sorption mechanisms. In a co-solute system, the sorption affinity of sitagliptin on the soil decreased with increasing metformin concentrations, suggesting that competitive sorption may reduce the sorption capacity of individual contaminants in soil systems containing multiple PPCPs.

Capture and recover dissolved phosphorous from aqueous solutions by a designer biochar: Mechanism and performance insights.

Excessive phosphorus (P) in marine and freshwater systems has been identified as a primary perpetrator for the harmful and nuisance algal blooms. In this study, a novel designer biochar was produced from sawdust biomass treated with lime sludge prior to pyrolysis. The adsorption of dissolved P on the designer biochar was comprehensively evaluated under different experimental conditions. It revealed that the removal of dissolved P by the designer biochar was more efficient than unmodified biochar, lime sludge, and their post-combination, suggesting that the pretreatment of biomass with lime sludge for the designer biochar production has a significantly synergic effect on enhancing P removal. Post-adsorption characterization and mathematical modeling analyses indicated that the adsorption of dissolved P on the designer biochar could be controlled by multiple mechanisms including physical and chemical adsorption. The precipitation reaction between P anions and metal ions on the surface of the designer biochar was identified as a predominant mechanism. The X-ray diffraction showed that the precipitation reaction generated a series of P fertilizer forms depositing onto the designer biochar. In addition, batch adsorption experiments showed that both initial solution pH and coexisting anions had a lesser effect on the P removal by the designer biochar. This study proposed that the designer biochar could be a promising sorbent to remove dissolved P, and the nutrient-captured biochar could be used as a fertilizer to recover nutrients.

Effective delignification of lignocellulosic biomass by microwave assisted deep eutectic solvents.

To establish an environmentally friendly and cheaper method to delignify lignocellulosic biomass feedstocks, deep eutectic solvents (DESs) were investigated as a green alternatives to conventional solvents. Six different DESs were facilely prepared and used to delignify miscanthus and birchwood feedstocks, including monocarboxylic acid/choline chloride (ChCl), dicarboxylic acid/ChCl and polyalcohol/ChCl. The enhanced delignification efficiency was evaluated in relation to the nature of the hydrogen bond donors and acid strength of DES. The largest extraction of lignin from the miscanthus and birchwood was achieved using ChCl.formic acid and ChCl.oxalic acid DES, respectively. The TGA and 13C NMR characterization results of the extracted lignin samples indicated that the different types of lignin were produced using different DESs. The reaction optimization results showed an increase in lignin extraction with increasing temperature from 60 to 130 °C. However, the optimal reaction time was different, 30 min for miscanthus and 60 min for birchwood. A convenient and reliable method for the quantification of lignin was developed using UV-Vis spectrophotometry.

Photobioreactor cultivation strategies for microalgae and cyanobacteria.

The current burden on fossil-derived chemicals and fuels combined with the rapidly increasing global population has led to a crucial need to develop renewable and sustainable sources of chemicals and biofuels. Photoautotrophic microorganisms, including cyanobacteria and microalgae, have garnered a great deal of attention for their capability to produce these chemicals from carbon dioxide, mineralized water, and solar energy. While there have been substantial amounts of research directed at scaling-up production from these microorganisms, several factors have proven difficult to overcome, including high costs associated with cultivation, photobioreactor construction, and artificial lighting. Decreasing these costs will substantially increase the economic feasibility of these production processes. Thus, the purpose of this review is to describe various photobioreactor designs, and then provide an overview on lighting systems, mixing, gas transfer, and the hydrodynamics of bubbles. These factors must be considered when the goal of a production process is economic feasibility. Targets for improving microalgae and cyanobacteria cultivation media, including water reduction strategies will also be described. As fossil fuel reserves continue to be depleted and the world population continues to increase, it is imperative that renewable chemical and biofuel production processes be developed toward becoming economically feasible. Thus, it is essential that future research is directed toward improving these processes. © 2018 American Institute of Chemical Engineers Biotechnol. Prog., 34:811-827, 2018.