The potential of WHR/batch and cullet preheating for energy efficiency in the EU ETS glass industry and the related energy incentives

The European Emissions Trading Scheme (EU ETS) covers approximately 45% of European greenhouse gases (GHGs), 11,000 stationary installations as well as aircraft operators. The EU ETS particularly affects the energy-intensive industries while it imposes a significant risk of “carbon leakage,” i.e., the risk of EU industry departing to countries with weaker restraints on GHG emissions. The EU glass industry, being capital intensive and also requiring long investment cycles, is the world’s largest glass producer with a market share close to one third of global production. Therefore, it is of significant importance to view the position of the EU ETS glass industry in terms of energy conservation possibilities. The present paper utilizes a vertical approach to provide information on both ETS market evolution and specific technical information to support technological innovation to the glass industry. EU ETS glass industry is analyzed regarding the balance between allocated European Union emission allowances (EUAs), verified CO₂ emissions, and potential shortfall in allowances so as to determine the situation of glass industries and the extent of urge for energy-saving activities towards the strengthening of their position within the requirements of the EU ETS phase III. The replication potential of waste heat recovery (WHR) through batch preheating is specifically addressed since it is considered a promising technology according to the latest Best Available Techniques (BAT) reference document for the glass industry under Directive IED 2010/75/EU. A case study for a container glass furnace based on simulation results is presented investigating the impact of different operating and design configurations on specific energy consumption and CO₂ emissions.     

Effects of water parameters on the degradation of microcystin-LR under visible light-activated TiO2 photocatalyst

A study was performed to determine the effect of pH, alkalinity, natural organic matter (NOM) and dissolved oxygen in the performance of nitrogen and fluorine doped TiO₂ (NF-TiO₂) for the degradation of hepatotoxin microcystin-LR (MC-LR) in synthetic and natural water under visible light irradiation. The initial degradation rate of MC-LR was fastest under acidic conditions (3.50 ± 0.02 × 10⁻³ μM min⁻¹ at pH 3.0) and decreased to 2.29 ± 0.07 × 10⁻³ and 0.54 ± 0.02 × 10⁻³ μM min⁻¹ at pH 5.7 and 7.1, respectively. Attractive forces between the opposite charged MC-LR and NF-TiO₂ are likely responsible for the enhancement in the photocatalytic decomposition of MC-LR resulting from increased interfacial adsorption. For carbonate buffered solutions, the photocatalytic activity of NF-TiO₂ was reduced when increasing the carbonate concentration up to 150 mg CaCO₃ L⁻¹. The scavenging of radical species by the bicarbonate ion at pH 7.1 is discussed. In the presence of NOM, the degradation rates decreased as pH and initial concentration of the NOM increased. The inhibition was higher with fulvic acid than humic acid under alkaline conditions. Oxygenated solution yields higher NF-TiO₂ photocatalytic degradation of MC-LR compared to nitrogen sparged solution at pH 5.7. The involvement of specific reactive oxygen species implicated in the photodegradation is proposed. Finally, no significant degradation is observed with various natural waters spiked with MC-LR under visible light (λ > 420 nm) but high removal was achieved with simulated solar light. This study provides a better understanding of the interactions and photocatalytic processes initiated by NF-TiO₂ under visible and solar light. The results indicate solar photocatalytic oxidation is a promising technology for the treatment of water contaminated with cyanotoxins.     

Handling zero in diminished-one modulo 2 n + 1 adders

Zero treatment in diminished-one modulo 2 ⁿ + 1 addition has traditionally been performed separately, leading to slow and area-consuming implementations. To overcome this, on the basis of an enhanced number representation used previously, we introduce novel carry look ahead and parallel-prefix architectures for diminished-one modulo 2 ⁿ + 1 adders that can also handle operands equal to 0. Translators for the new representation are also given.     

Construction and Applications of a Microcomputer Controlled Pulsed Amperometric Detector System

ABSTRACT

The construction of a microcomputer controlled pulsed amperometric detector system is described. It includes a potentiostat, a flow-through cell and a sample injection unit. The microcomputer generates the appropriate waveform of the applied potential and controls the overall sequence of the measurement. The system is suitable for general studies on the detection of various classes of organic compounds with the pulsed amperometric technique. The detectability of various hydroxycompounds has been studied.     

Implementation of a high speed frequency synthesizer employing a dual input phase accumulator

We present a new PLL based frequency synthesizer, in which we have replaced the conventional phase frequency detector and the dividers (programmable counters) with a sequential dual input phase accumulator (DIPA), consisting of a digital circuit employing adders, registers and a ladder. The main feature of the DIPA is that the two input frequencies are not required to be normalized (divided down) to the step frequency of the synthesizer. Instead, the two different high frequencies, that is the reference and the output frequency of the synthesizer, are applied directly. The DIPA samples and normalizes their phases at very high rates, calculates their phase difference, producing an output that consists of a dc component proportional to the phase difference and harmonics of the two input high frequencies. These harmonics are high frequencies and can easily be rejected by a wide bandwidth filter of the loop, without affecting the high convergence speed of the loop. Moreover, these harmonics do not generate spurs near the output frequency. The resolution of the DIPA based synthesizer depends only on the length of the digital word of the DIPA, and its convergence speed depends on the lower of the two input frequencies. The output of the DIPA is a linear function of the phase difference of the two input frequencies and its dynamic range exceeds the limit of ±2π that governs the conventional phase detectors. Thus, the proposed frequency synthesizer based on the DIPA has low phase noise, no spurs nearby the output frequency, high resolution and fast convergence rate. Additionally, the output frequency can be digitally modulated under the control of the closed loop, either by phase or frequency modulation.     

The Effects of P-Poisoning of CexZr1−xO2 on the Transient Oxygen Storage and Release Kinetics

The present work reports on the investigation of the effects of chemical poisoning of Ce_xZr_1?xO₂ solids by phosphorous (P) on the kinetics of oxygen storage and release (OSR) of the thus derived P-contaminated solids, as a function of Ce_xZr_1?xO₂ solid composition (x = 0.3, 0.5 and 0.7) for the first time. Phosphorous deposition on the surface of Ce_xZr_1?xO₂ particles followed by calcination in air at 850 °C forms nano-crystals of CePO₄, which lead to a drastic decrease in the population of surface and subsurface reactive and mobile oxygen species due to the formation of P–O–Ce bonding. The concentration (μmol/g) of exchangeable ¹⁶O in the solid with ¹⁸O from the gas phase was found to increase, and the degree of reduction in the Oxygen Storage Capacity (OSC) to decrease with increasing Ce content in the Ce_xZr_1?xO₂ solid after P-poisoning. The increase in the Ce content of Ce_xZr_1?xO₂ makes its OSR properties more resistant against P-poisoning due to the increasing number of poison-free Ce atoms, which are able to participate in the Ce³⁺ ? Ce⁴⁺ redox cycle.     

The CH4/NO/O2 “Lean-deNOx” Reaction on Mesoporous Mn-Based Mixed Oxides

High surface area Mn-based porous oxides (MANPO) containing additives like Ce, Sr and La were found to be very active and selective materials under 0.67% CH₄/0.2% NO/5% O₂ lean-deNO _x conditions in the 200–300°C low-temperature range. These materials perform also impressively in the presence of 4% H₂O in the feed stream, where a N₂ selectivity of 98% and an excellent stability over 24 h on stream have been observed. The MANPO materials can be considered serious competitors of noble metals for low-temperature lean-deNO _x applications.     

A two-step reaction mechanism of oxygen release from Pd/CeO2: mathematical modelling based on step gas concentration experiments

Topics in Catalysis - A mathematical model has been developed to study the transient release of oxygen from a 1 wt% Pd/CeO2 catalyst in the 450–550 °C range based on alternate...     

Nucleation of isolated PO4 units on CeO2 driven by high temperatures and the effect on its oxygen storage and release properties

The chemical nature of P-containing species of varying concentration present in CeO₂ after impregnation with (NH₄)₂HPO₄ and calcination at 1273 K, and their effects on the oxygen storage and release (OSR) properties of ceria are reported for the first time. The samples were characterized by different techniques and the results were compared with those recently reported on the same samples but calcined at 873 K. When P-containing ceria solids were calcined at 1273 K, CePO₄ (monazite) was the predominant P-containing species on the surface of ceria, confirming previous studies that showed that monazite exists for those samples in which the surface P loading (P atoms per nm⁻²) is larger than 5.5. For lower surface P concentrations, isolated orthophosphate units are present at the surface and within the subsurface region of the solid. Severe sintering of CeO₂ after calcination at 1273 K resulted in P concentrations >5.5 P atoms·nm⁻² in all samples. Isolated PO₄ units that could initially be present in the samples calcined at 873 K nucleated and CePO₄ was formed when samples were calcined at 1273 K. OSR properties of CeO₂ deteriorated progressively when P loading increased due to the presence of larger crystals of the very stable Ce(III) phase of CePO₄ at the surface of the P-containing ceria solids.