Reinforced degradation of ibuprofen with MnCo2O4/FCNTs nanocatalyst as peroxymonosulfate activator : Performance and mechanism

In order to efficiently degrade ibuprofen (IBU) by peroxymonosulfate (PMS) activation, manganese cobalt oxide nanoparticles-decorated functionalized multi-walled carbon nanotubes (MnCo2O4/FCNTs) were prepared using a facile hydrothermal method. Comprehensive characterization of this PMS activator in multi-scale suggested that MnCo2O4 nanoparticles were uniformly decorated on FCNTs. The catalytic performance was systematical evaluated under various environmental conditions, including temperature, pH, and the presence of different common water matrix species (e.g., Cl-, HCO3-, and natural organic matter). The as-synthesized MnCo2O4/FCNTs demonstrated excellent catalytic activity with kapp ranging 0.285-0.327 min-1 under a wide pH range of 3-9 within 10 min, which achieved a complete removal of IBU and a mineralization rate higher than 90%. During oxidation process for stability and reusability test, recycled MnCo2O4/FCNTs was found durable with negligible leaching of metal ions from spent catalyst, exhibiting its high stability for PMS activation with merely slight decrease of kapp from 0.285 to 0.201 min-1 in the fourth cycle. Electron paramagnetic resonance analysis further confirmed that •OH, SO4•- and 1O2 were generated in the robust MnCo2O4/FCNTs-PMS system. Both radical and nonradical reactions were found to be responsible for the enhanced IBU degradation. Overall, this study sheds light on practical knowledge of IBU removal using MnCo2O4/FCNTs for PMS activation.publishedVersionPeer reviewe

The role of ubiquitous metal ions in degradation of microplastics in hot-compressed water

Hydrothermal processing (HTP) is an efficient thermochemical technology to achieve sound treatment and resource recovery of sewage sludge (SS) in hot-compressed subcritical water. However, microplastics (MPs) and heavy metals can be problematic impurities for high-quality nutrients recovery from SS. This study initiated hydrothermal degradation of representative MPs (i.e., polyethylene (PE), polyamide (PA), polypropylene (PP)) under varied temperatures (180–300 °C) to understand the effect of four ubiquitous metal ions (i.e., Fe3+, Al3+, Cu2+, Zn2+) on MPs degradation. It was found that weight loss of all MPs in metallic reaction media was almost four times of that in water media, indicating the catalytic role of metal ions in HTP. Especially, PA degradation at 300 °C was promoted by Fe3+ and Al3+ with remarkable weight loss higher than 95% and 92%, respectively, which was ca. 160 °C lower than that in pyrolysis. Nevertheless, PE and PP were more recalcitrant polymers to be degraded under identical condition. Although higher temperature thermal hydrolysis reaction induced severe chain scission of polymers to reinforce degradation of MPs, Fe3+ and Al3+ ions demonstrated the most remarkable catalytic depolymerization of MPs via enhanced free radical dissociation rather than hydrolysis. Pyrolysis gas chromatography-mass spectrometry (Py GC–MS) was further complementarily applied with GC–MS to reveal HTP of MPs to secondary MPs and nanoplastics. This fundamental study highlights the crucial role of ubiquitous metal ions in MPs degradation in hot-compressed water. HTP could be an energy-efficient technology for effective treatment of MPs in SS with abundant Fe3+ and Al3+, which will benefit sustainable recovery of cleaner nutrients in hydrochar and value-added chemicals or monomers from MPs.publishedVersionPeer reviewe

A Sugarcane-Bagasse-Based Adsorbent Employed for Mitigating Eutrophication Threats and Producing Biodiesel Simultaneously

Eutrophication is an inevitable phenomenon, and it has recently become an unabated threat. As a positive, the thriving microalgal biomass in eutrophic water is conventionally perceived to be loaded with myriad valuable biochemical compounds. Therefore, a sugarcane-bagasse-based adsorbent was proposed in this study to harvest the microalgal biomass for producing biodiesel. By activating the sugarcane-bagasse-based adsorbent with 1.5 M of H2SO4, a highest adsorption capacity of 108.9 ± 0.3 mg/g was attained. This was fundamentally due to the surface potential of the 1.5 M H2SO4 acid-modified sugarcane-bagasse-based adsorbent possessing the lowest surface positivity value as calculated from its point of zero charge. The adsorption capacity was then improved to 192.9 ± 0.1 mg/g by stepwise optimizing the adsorbent size to 6.7–8.0 mm, adsorption medium pH to 2–4, and adsorbent dosage to 0.4 g per 100 mL of adsorption medium. This resulted in 91.5% microalgae removal efficiency. Excellent-quality biodiesel was also obtained as reflected by the fatty acid methyl ester (FAME) profile, showing the dominant species of C16–C18 encompassing 71% of the overall FAMEs. The sustainability of harvesting microalgal biomass via an adsorption-enhanced flocculation processes was also evidenced by the potentiality to reuse the spent acid-modified adsorbent

Sunlight mediated enhanced removal of metoprolol using graphitic carbon nitride (g-C3N4)

Graphitic carbon nitride (g-C3N4) is a photocatalyst that has recently been given a lot of attention due to its effectiveness in wastewater and environmental treatment, solar energy utilization, biomedical applications, etc. In this study, g-C3N4 was synthesized and characterized to carry out the degradation of metoprolol tartrate salt (MET), which is classified as an emerging contaminant. MET is one of the most commonly used pharmaceuticals to treat patients with cardiovascular diseases and disorders, a common disease in Malaysia. Recent discoveries of MET in surface waters and drinking water raise awareness and concerns. g-C3N4 was synthesized using solid urea by placing it in a muffle furnace of 550°C for 3 hours. The photocatalytic activities of g-C3N4 were investigated by photodegradation of MET, g-C3N4 of different dosages were added into MET-containing solution, and a dark reaction was carried out for 24 hours for complete adsorption equilibrium. Various physical and chemical analyses were conducted to elucidate the properties of g-C3N4, such as FESEM, FTIR and UV-Vis. The absorbance and reflectance graphs of g-C3N4 show that there will be higher absorption in the visible light spectra. The results show that the optimum dosage to treat 10 ppm of MET is by using 0.3 g of g-C3N4. Under sunlight irradiation of 4 hours, the degradation of MET achieved 54.6% of removal. Hence, it proves that g-C3N4 nanosheet can be applied to remove complex pollutants such as MET under sunlight irradiation. This path is an alternative removal method for MET in a sustainable approach

Enhanced catalytic soot oxidation by Ce-based MOF-derived ceria nano-bar with promoted oxygen vacancy

As CeO2 is a useful catalyst for soot elimination, it is important to develop CeO2 with higher contact areas, and reactivities for efficient soot oxidation and catalytic soot oxidation are basically controlled by structures and surface properties of catalysts. Herein, a Ce-Metal organic framework (MOFs) consisting of Ce and benzene-1,3,5-tricarboxylic acid (H3BTC) is employed as the precursor as CeBTC exhibits a unique bar-like high-aspect-ratio morphology, which is then transformed into CeO2 with a nanoscale bar-like configuration. More importantly, this CeO2 nanobar (CeONB) possesses porou, and even hollow structures, as well as more oxygen vacancies, enabling CeONB to become a promising catalyst for soot oxidation. Thus, CeONB shows a much higher catalytic activity than commercial CeO2 nanoparticle (comCeO) for soot oxidation with a significantly lower ignition temperature (Tig). Moreover, while soot oxidation by comCeO leads to production of CO together with CO2, CeONB can completely convert soot to CO2. The tight contact mode also enables CeONB to exhibit a very low Tig of 310 °C, whereas the existence of NO also enhances the soot oxidation by CeONB to reduce the Tig. The mechanism of NO-assisted soot oxidation is also examined, and validated by DRIFTS to identify the formation and transformation of nitrogen-containing intermediates. CeONB is also recyclable over many consecutive cycles and maintained its high catalytic activity for soot oxidation. These results demonstrate that CeONB is a promising and easily prepared high-aspect-ratio Ce-based catalyst for soot oxidation

Advances in MRI Assessment of Gliomas and Response to Anti-VEGF Therapy

Bevacizumab is thought to normalize tumor vasculature and restore the blood–brain barrier, decreasing enhancement and peritumoral edema. Conventional measurements of tumor response rely upon dimensions of enhancing tumor. After bevacizumab treatment, glioblastomas are more prone to progress as nonenhancing tumor. The RANO (Response Assessment in Neuro-Oncology) criteria for glioma response use fluid-attenuated inversion recovery (FLAIR)/T2 hyperintensity as a surrogate for nonenhancing tumor; however, nonenhancing tumor can be difficult to differentiate from other causes of FLAIR/T2 hyperintensity (eg, radiation-induced gliosis). Due to these difficulties, recent efforts have been directed toward identifying new biomarkers that either predict treatment response or accurately measure response of both enhancing and nonenhancing tumor shortly after treatment initiation. This will allow for earlier treatment decisions, saving patients from the adverse effects of ineffective therapies while allowing them to try alternative therapies sooner. An active area of research is the use of physiologic imaging, which can potentially detect treatment effects before changes in tumor size are evident

The chlorosome: a prototype for efficient light harvesting in photosynthesis

Three phyla of bacteria include phototrophs that contain unique antenna systems, chlorosomes, as the principal light-harvesting apparatus. Chlorosomes are the largest known supramolecular antenna systems and contain hundreds of thousands of BChl c/d/e molecules enclosed by a single membrane leaflet and a baseplate. The BChl pigments are organized via self-assembly and do not require proteins to provide a scaffold for efficient light harvesting. Their excitation energy flows via a small protein, CsmA embedded in the baseplate to the photosynthetic reaction centres. Chlorosomes allow for photosynthesis at very low light intensities by ultra-rapid transfer of excitations to reaction centres and enable organisms with chlorosomes to live at extraordinarily low light intensities under which no other phototrophic organisms can grow. This article reviews several aspects of chlorosomes: the supramolecular and molecular organizations and the light-harvesting and spectroscopic properties. In addition, it provides some novel information about the organization of the baseplate

Jet energy measurement with the ATLAS detector in proton-proton collisions at root s=7 TeV

The jet energy scale and its systematic uncertainty are determined for jets measured with the ATLAS detector at the LHC in proton-proton collision data at a centre-of-mass energy of √s = 7TeV corresponding to an integrated luminosity of 38 pb-1. Jets are reconstructed with the anti-kt algorithm with distance parameters R=0. 4 or R=0. 6. Jet energy and angle corrections are determined from Monte Carlo simulations to calibrate jets with transverse momenta pT≥20 GeV and pseudorapidities {pipe}η{pipe}<4. 5. The jet energy systematic uncertainty is estimated using the single isolated hadron response measured in situ and in test-beams, exploiting the transverse momentum balance between central and forward jets in events with dijet topologies and studying systematic variations in Monte Carlo simulations. The jet energy uncertainty is less than 2. 5 % in the central calorimeter region ({pipe}η{pipe}<0. 8) for jets with 60≤pT<800 GeV, and is maximally 14 % for pT<30 GeV in the most forward region 3. 2≤{pipe}η{pipe}<4. 5. The jet energy is validated for jet transverse momenta up to 1 TeV to the level of a few percent using several in situ techniques by comparing a well-known reference such as the recoiling photon pT, the sum of the transverse momenta of tracks associated to the jet, or a system of low-pT jets recoiling against a high-pT jet. More sophisticated jet calibration schemes are presented based on calorimeter cell energy density weighting or hadronic properties of jets, aiming for an improved jet energy resolution and a reduced flavour dependence of the jet response. The systematic uncertainty of the jet energy determined from a combination of in situ techniques is consistent with the one derived from single hadron response measurements over a wide kinematic range. The nominal corrections and uncertainties are derived for isolated jets in an inclusive sample of high-pT jets. Special cases such as event topologies with close-by jets, or selections of samples with an enhanced content of jets originating from light quarks, heavy quarks or gluons are also discussed and the corresponding uncertainties are determined. © 2013 CERN for the benefit of the ATLAS collaboration