Biochar application in organics and ultra-violet quenching substances removal from sludge dewatering leachate for algae production.

Algae production in nutrient rich sludge dewatering leachate after biogas production is a promising option for wastewater treatment plants. However, the ultra-violet (UV) absorbing characteristic of UV-quenching substances (UVQS) existing in these waters can notably reduce the light transmission within the liquid body. The present work demonstrates a comparative adsorptive removal of UVQS, and other organic substances (expressed as COD and TOC) onto the "acid catalyst" functionalised adsorbent (PPhA) and commercial activated carbon (CAC) from leachate originating from leftover sludge dewatering after biogas production. Laboratory scale column studies were performed to investigate the adsorption performance of selected parameters. The PPhA increased the UV transmittance of leachate more than 4 times and outperformed CAC. Bed Depth Service Time and Yan models were used on the experimental data in order to estimate the maximum adsorption capacity and evaluate the characteristics of the fixed-bed. The PPhA equilibrium uptake of COD and TOC amounted to 5.7 mg/g and 0.9 mg/g, respectively. The postulated removal mechanism in environmentally relevant conditions (e.g., pH neutral) suggested a complex interaction between the biochar and organic macromolecules. Diluted phosphoric acid solution (0.01 mol/L) was successfully used for the column regeneration. Beside the UVQS, PPhA showed affinity towards toxic heavy metals (e.g., Pb, Ni, Co) pointing out the rich surface chemistry of the PPhA. Based on the obtained results and successfully implemented scale-up methodology, the low-cost PPhA adsorbent might effectively compete with the CAC as a highly efficient platform in wastewaters leachate processing.

Microbial fuel cell biosensor for the determination of biochemical oxygen demand of wastewater samples containing readily and slowly biodegradable organics.

OBJECTIVES: Single-chamber air cathode microbial fuel cells (MFCs) were applied as biosensors for biochemical oxygen demand (BOD) measurement of real wastewaters with considerable suspended and/or slowly biodegradable organic content. RESULTS: The measurement method consists of batch sample injection, continuous measurement of cell voltage and calculation of total charge (Q) gained during the biodegradation of organic content. Diverse samples were analyzed: acetate and peptone samples containing only soluble readily biodegradable substrates; corn starch and milk samples with suspended and colloidal organics; real domestic and brewery wastewaters. Linear regression fitted to the Q vs. BOD5 measurement points of the real wastewaters provided high (> 0.985) R2 values. Time requirement of the measurement varied from 1 to 4 days, depending on the composition of the sample. CONCLUSIONS: Relative error of BOD measured in the MFCs comparing with BOD5 was less than 10%, thus the method might be a good basis for the development of on-site automatic BOD sensors for real wastewater samples.

Single chamber air-cathode microbial fuel cells as biosensors for determination of biodegradable organics.

OBJECTIVES: Single chamber air cathode microbial fuel cells (MFCs) were investigated with sodium-acetate and peptone as test substrates to assess the potential for application as biosensor to determine the concentration of biodegradable organics in water/wastewater samples. RESULTS: MFCs provided well-reproducible performance at high (> 2000 mg COD l-1-Chemical Oxygen Demand) acetate concentration values. Current in the cells proved to be steady from 25 to 35 °C, significant decrease was, however, revealed in the current below 20 °C. Direct calculation of non-toxic biodegradable substrate concentration in water/wastewater from the current in MFCs is possible only in the non-saturated substrate concentration range due to the Monod-like dependence of the current. This range was determined by a fitted and verified Monod-based kinetic model. Half saturation constant (KS) values were calculated at 30 °C applying different external resistance values (100 Ω, 600 Ω and 1000 Ω, respectively). In each case KS remained below 10 mg COD l-1. CONCLUSIONS: Biosensors with this particular MFC design and operation are potentially applicable for detecting as low as 5 mg COD l-1 readily biodegradable substrates, and measuring the concentration of these substances up to ~ 50-70 mg COD l-1.

Cellulase production using different streams of wheat grain- and wheat straw-based ethanol processes.

Pretreatment is a necessary step in the biomass-to-ethanol conversion process. The side stream of the pretreatment step is the liquid fraction, also referred to as the hydrolyzate, which arises after the separation of the pretreated solid and is composed of valuable carbohydrates along with compounds that are potentially toxic to microbes (mainly furfural, acetic acid, and formic acid). The aim of our study was to utilize the liquid fraction from steam-exploded wheat straw as a carbon source for cellulase production by Trichoderma reesei RUT C30. Results showed that without detoxification, the fungus failed to utilize any dilution of the hydrolyzate; however, after a two-step detoxification process, it was able to grow on a fourfold dilution of the treated liquid fraction. Supplementation of the fourfold-diluted, treated liquid fraction with washed pretreated wheat straw or ground wheat grain led to enhanced cellulase (filter paper) activity. Produced enzymes were tested in hydrolysis of washed pretreated wheat straw. Supplementation with ground wheat grain provided a more efficient enzyme mixture for the hydrolysis by means of the near-doubled ß-glucosidase activity obtained.

Relevance of the light signaling machinery for cellulase expression in Trichoderma reesei (Hypocrea jecorina).

BACKGROUND: In nature, light is one of the most important environmental cues that fungi perceive and interpret. It is known not only to influence growth and conidiation, but also cellulase gene expression. We therefore studied the relevance of the main components of the light perception machinery of Trichoderma reesei (Hypocrea jecorina), ENV1, BLR1 and BLR2, for production of plant cell wall degrading enzymes in fermentations aimed at efficient biosynthesis of enzyme mixtures for biofuel production. FINDINGS: Our results indicate that despite cultivation in mostly dark conditions, all three components show an influence on cellulase expression. While we found the performance of the enzyme mixture secreted by a deletion mutant in env1 to be enhanced, the higher cellulolytic activity observed for Δblr2 is mainly due to an increased secretion capacity of this strain. Δblr1 showed enhanced biomass accumulation, but due to its obviously lower secretion capacity still was the least efficient strain in this study. CONCLUSIONS: We conclude that with respect to regulation of plant cell wall degrading enzymes, the blue light regulator proteins are unlikely to act as a complex. Their regulatory influence on cellulase biosynthesis involves an alteration of protein secretion, which may be due to adjustment of transcription or posttranscriptional regulation of upstream factors. In contrast, the regulatory function of ENV1 seems to involve adjustment of enzyme proportions to environmental conditions.