Recycle,Bury, or Burn Wood Waste Biomass?: LCA Answer Depends on Carbon Accounting,Emissions Controls,Displaced Fuels,and Impact Costs

This study extends existing life cycle assessment (LCA) literature by assessing seven environmental burdens and an overall monetized environmental score for eight recycle, bury, or burn options to manage clean wood wastes generated at construction and demolition activity sites. The study assesses direct environmental impacts along with substitution effects from displacing fossil fuels and managed forest wood sourcing activities. Follow‐on effects on forest carbon stocks, land use, and fuel markets are not assessed. Sensitivity analysis addresses landfill carbon storage and biodegradation rates, atmospheric emissions controls, displaced fuel types, and two alternative carbon accounting methods commonly used for waste management LCAs. Base‐case carbon accounting considers emissions and uptakes of all biogenic and fossil carbon compounds, including biogenic carbon dioxide. Base‐case results show that recycling options (recycling into reconstituted wood products or into wood pulp for papermaking) rank better than all burning or burying options for overall monetized score as well as for climate impacts, except that wood substitution for coal in industrial boilers is slightly better than recycling for the climate. Wood substitution for natural gas boiler fuel has the highest environmental impacts. Sensitivity analysis shows the overall monetized score rankings for recycling options to be robust except for the carbon accounting method, for which all options are highly sensitive. Under one of the alternative methods, wood substitution for coal boiler fuel and landfill options with high methane capture efficiency are the best for the overall score; recycling options are next to the worst. Under the other accounting alternative, wood substitution for coal and waste‐to‐energy are the best, followed by recycling options.     

The Potential Role of Reactive Metals for a Clean Energy Transition

Reactive metal‐based storage systems are a new alternative to support the clean energy transition. Herein, the cases of Al and Na are presented, both preliminarily fulfilling the constraints regarding sustainability, but employing two rather different processes. Both, the steam combustion of molten Al for H₂ and heat production, and a new rechargeable battery, which makes use of seawater and sodium as electrodes, show promising round‐trip efficiencies. The latter technology also allows CO₂‐trapping, desalination, Na metal, and chlorine production. It is argued that further research efforts are needed to verify the sustainability and ability of reactive metal‐based technologies to compete with other storage technologies.     

Impact of ligand environment on optical,luminescence and thermometric behavior of A3(PO4)2:Sm3+ (A = Ca,Sr) phosphors

The present study investigates the impact of the ligand environment on the luminescence and thermometric behavior of Sm³⁺ doped A₃(PO₄)₂ (A = Sr, Ca) phosphors prepared by combustion synthesis. The structural and luminescent properties of Sm³⁺ ions in the phosphate lattices were investigated using powder X-ray diffraction (PXRD) and photoluminescence (PL) techniques. PXRD results of the synthesized phosphors exhibit the expected phases that are in agreement with their respective standards. Fourier-transform infrared (FTIR) spectroscopy confirms the presence of PO₄ vibrational bands. Upon excitation with near ultraviolet light, the PL studies indicated that Sr₃(PO₄)₂:Sm³⁺ phosphors exhibit a yellow light emission, whereas Ca₃(PO₄)₂:Sm³⁺ phosphors exhibit an emission of orange light. The PL emission results are in accordance with the CIE coordinates, with the Sr₃(PO₄)₂:Sm³⁺ phosphors showing coordinates of (0.56, 0.44), and the Ca₃(PO₄)₂:Sm³⁺ phosphors displaying coordinates of (0.60, 0.40). Thermal analysis shows improved stability of Ca₃(PO₄)₂:Sm³⁺ based on lower weight reduction in thermogravimetric analysis. The effect of temperature on the luminescence properties of the phosphor has been examined upon a 405 nm excitation. By using the fluorescence intensity ratio (FIR) method, the temperature responses of the emission ratios from the Sm³⁺: the ⁴F_3/2 → ⁶H_5/2 transition to the ⁴G_5/2 → ⁶H_7/2 and ⁴F_3/2 → ⁶H_5/2 transition to the ⁴G_5/2 → ⁶H_9/2 emissions are characterized. The Ca₃(PO₄)₂:Sm³⁺ phosphors are more sensitive as compared with the Sr₃(PO₄)₂:Sm³⁺ phosphors. The earlier research findings strongly indicate that these phosphors hold great promise as ideal candidates for applications in non-invasive optical thermometry and solid-state lighting devices.     

Green synthesis of ZnO hierarchical microstructures by Cordia myxa and their antibacterial activity

In this study, the leaves extract of Cordia myxa, has been used for the first time to synthesize zinc oxide (ZnO) hierarchical microstructures. The solution combustion method was employed as a self-sustaining reaction between zinc nitrate and the leaves extract. The surface properties of leaves mediated ZnO microstructures were determined by UV–Visible spectral analysis, Fourier transform infrared (FT-IR), Cold field emission-scanning electron microscopy (CFE-SEM), Energy dispersive X-ray (EDX), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). In addition, the effect of the leaves extract concentration on ZnO structures, size and surface properties was also studied. ZnO structures synthesized employing C. myxa were found to be hexagonal, triangular and round in shape which was determined using CFE-SEM. X-ray diffraction (XRD) analysis confirmed the crystalline nature of compounds. Furthermore, C. myxa mediated ZnO microstructures shows good bactericidal activity against Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria.     

Economic analysis of biomass power generation schemes under renewable energy initiative with Renewable Portfolio Standards (RPS) in Korea

An economic analysis of biomass power generation was conducted. Two key technologies--direct combustion with a steam turbine and gasification with a syngas engine--were mainly examined. In view of the present domestic biomass infrastructure of Korea, a small and distributed power generation system ranging from 0.5 to 5 MW(e) was considered. It was found that gasification with a syngas engine becomes more economically feasible as the plant size decreases. Changes in the economic feasibilities with and without RPS or heat sales were also investigated. A sensitivity analysis of each system was conducted for representative parameters. Regarding the cost of electricity generation, electrical efficiency and fuel cost significantly affect both direct combustion and gasification systems. Regarding the internal rate of return (IRR), the heat sales price becomes important for obtaining a higher IRR, followed by power generation capacity and electrical efficiency.     

腐殖质粒径和燃烧深度对兴安落叶松人工林地下火燃烧温度的影响

地下火是森林中难以控制的一种燃烧现象,对森林危害极大,燃烧所释放的温度影响着地下火蔓延。以我国地下火频发区域之一的大兴安岭地区兴安落叶松(Larix gmelinii)人工林为研究对象,通过室内控制模拟点烧实验的方法,研究腐殖质粒径和燃烧深度对地下火燃烧温度的影响。结果表明：在不同地类条件下,不同粒径腐殖质和深度对燃烧最高温度的影响存在显著差异(P<0.05);在不同深度条件下,不同地类和腐殖质粒径以及二者的交互作用对燃烧最高温度的影响均存在显著差异(P<0.05);在5种地类的腐殖质中都以粒径≤80目和深度12cm处的燃烧温度最高;塔头甸子和水湿地条件下的地下火燃烧温度较高,尤其是塔头甸子;深度、距离和腐殖质粒径可作为有坡山地、水湿地和农用地条件下预测模型自变量,深度和腐殖质粒径可作为塔头甸子和无坡山地条件下预测模型自变量,且模型均通过了显著性检验(P<0.05)。相关研究成果可以为该地区地下火的防控和扑火装备的研发提供科学依据。     

Photoluminescence and structural analysis of trivalent europium doped MLaAl3O7 (M = Ba,Ca, Mg and Sr) nanophosphors

The solution combustion technique was used to synthesize MLaAl₃O₇ (M = Ba, Ca, Mg, and Sr) nanophosphors‐doped with Eu³⁺ using metal nitrates as precursors. The photoluminescence (PL) emission spectra exhibited three peaks at 587–591, 610–616, and 653–654 corresponding to ⁵D₀→⁷F₁, ⁵D₀→⁷F₂, and ⁵D₀→⁷F₃ transitions, respectively. Upon excitation at 254 nm, these nanophosphors displayed strong red emission with the dominant peak attributed to the ⁵D₀→⁷F₂ transition of Eu³⁺. The materials were further heated at 900 and 1050°C for 2 h to examine the consequence of temperature on crystal lattice and PL emission intensity. X‐ray diffraction (XRD) analysis proved that all the synthesized materials were of a crystalline nature. CaLaAl₃O₇ material has a tetragonal crystal structure with space group P421m. Scherer's equation was used to calculate the crystallite size of synthesized phosphors using XRD data. A Fourier transformation infrared study was used to observe the stretching vibrations of metal–oxygen bonds. Infrared peaks for stretching vibrations corresponding to lanthanum–oxygen and aluminium–oxygen bonds were found at 582 and 777 cm^–1 respectively for CaLaAl₃O₇ phosphor material. Transmission electron microscopy images were used to determine the size of particles (18–37 nm for the as‐prepared materials) and also to analyze the three‐dimensional view of these materials. The experimental data indicate that these materials may be promising red‐emitting nanophosphors for use in white light‐emitting diodes.     

Combustion synthesis of blue‐emitting submicron CaAl4O7:Eu2+, Dy3+ persistence phosphor

Long persistence phosphor CaAl₄O₇: Eu²⁺, Dy³⁺ were prepared by a combustion method. The phosphors were characterized by means of X‐ray diffraction (XRD), scanning electron microscopy (SEM), decay time measurement techniques and photoluminescence spectra (PL). The CaAl₄O₇: Eu²⁺, Dy³⁺ phosphor showed a broad blue emission, peaking at 445 nm when excited at 341 nm. Such a blue emission can be attributed to the intrinsic 4f → 5d transitions of Eu²⁺ in the host lattices. The lifetime decay curve of the Dy³⁺ co‐doped CaAl₄O₇: Eu²⁺ phosphor contains a fast decay component and another slow decay one. Surface morphology also has been studied by SEM. The calculated CIE colour chromaticity coordinates was (0.227, 043). We have also discussed a possible long‐persistent mechanism of CaAl₄O₇:Eu²⁺, Dy³⁺ phosphor. All the results indicate that this phosphor has promising potential for practical applications in the field of long‐lasting phosphors for the purposes of sign boards and defence. Copyright © 2011 John Wiley & Sons, Ltd.     

Photoluminescence and thermoluminescence studies of CaAl2O4:Dy3+ phosphor

Calcium aluminate phosphors activated by Dy³⁺ have been prepared by a combustion method at a temperature of 600°C. Photoluminescence (PL) and thermoluminescence (TL) properties of gamma‐irradiated Dy‐doped calcium aluminate were investigated. The PL spectrum shows a broad peak around 488 nm and 573 nm, under 347 nm excitation. Thermoluminescence studies were performed for different concentrations of Dy. Optimum intensity of photoluminescence was found for 0.02 mol% concentration of Dy. It was found that initially the peak TL intensity increases with increasing concentration of Dy in the CaAl₂O₄ host, attains a maximum value for 0.05 mol% concentration and decreases with further increase in the doping concentration due to concentration quenching. Copyright © 2015 John Wiley & Sons, Ltd.     

High‐Performance Ultrathin Co3O4 Nanosheet Supported PdO/CeO2 Catalysts for Methane Combustion

Efficient utilization of methane via catalytic complete combustion is a very important pathway to realize energy efficiency and pollution reduction. From the viewpoint of structural design, herein a green water‐phase route is developed to prepare ultrathin Co(OH)₂ nanosheet supported Pd catalysts. As a platform, the as‐obtained Pd/Co(OH)₂ nanosheets are able to be further used to load CeO₂ nanoparticles to form 2D nanostructured Pd/CeO₂/Co(OH)₂ multicomponent hybrids, and further calcination can result in the final well‐crystallized ultrathin Co₃O₄ nanosheet supported PdO/CeO₂ catalysts. Catalytic tests on methane combustion reveal that CeO₂ as a catalytic assistant greatly boosts the catalytic performance of PdO/Co₃O₄ via strong synergetic effects with Pd species and Co₃O₄ components. The best sample of PdO/CeO₂‐0.1/Co₃O₄ exhibits surprisingly enhanced light‐off activity, indicating that such 2D Co₃O₄ nanosheet supported nanocatalysts might show promising prospect for heterogeneous catalysis.