Neoclassical Growth, Environment and Technological Change: The Environmental Kuznets Curve

The paper investigates socially optimal patterns of economic growth and environmental quality in a neoclassical growth model with endogenous technological progress. In the model, the environmental quality affects positively not only to utility but also to production. However, cleaner technologies can be used in the economy whether a part of the output is used in environmentally oriented R&D. In this framework, if the initial level of capital is low then the shadow price of a cleaner technology is low relative to the cost of developing it given by the marginal utility of consumption and it is not worth investing in R&D. Thus, there will be a first stage of growth based only on the accumulation of capital with a decreasing environmental quality until the moment that pollution is great enough to make profitable the investment in R&D. After this turning point, if the new technologies are efficient enough, the economy can evolve along a balanced growth path with an increasing environmental quality. The result is that the optimal investment pattern supports an environmental Kuznets curve.Neoclassical Growth Model, Endogenous Technological Progress, External Effects, Environmental Kuznets Curve

In situ temperature measurements in microwave-heated gassolid catalytic systems. Detection of hot spots and solid-fluid temperature gradients in the ethylene epoxidation reaction

Infrared thermographic techniques have been used for the first time to determine real-time gas and solid temperatures, as well as gas- solid temperature gradients in microwave heated structured reactors. A special reactor vessel has been developed that allows direct observation of the catalyst under microwave heating, and an operating procedure is presented to obtain gas and solid apparent emissivities as a function of temperature. These values are thereafter used to calculate temperatures at any point in the gas and solid phases under reaction. The method has been used to obtain gas and solid temperatures during the ethylene epoxidation reaction carried out on a silver-copper oxide catalyst. The direct heating of the monolith walls produced a stable, large temperature gradient between the solid and the gas phase

Recent advances in the design and photocatalytic enhanced performance of gold plasmonic nanostructures decorated with non-titania based semiconductor hetero-nanoarchitectures

Plasmonic photocatalysts combining metallic nanoparticles and semiconductors have been aimed as versatile alternatives to drive light-assisted catalytic chemical reactions beyond the ultraviolet (UV) regions, and overcome one of the major drawbacks of the most exploited photocatalysts (TiO2 or ZnO). The strong size and morphology dependence of metallic nanostructures to tune their visible to near-infrared (vis-NIR) light harvesting capabilities has been combined with the design of a wide variety of architectures for the semiconductor supports to promote the selective activity of specific crystallographic facets. The search for efficient heterojunctions has been subjected to numerous studies, especially those involving gold nanostructures and titania semiconductors. In the present review, we paid special attention to the most recent advances in the design of gold-semiconductor hetero-nanostructures including emerging metal oxides such as cerium oxide or copper oxide (CeO2 or Cu2O) or metal chalcogenides such as copper sulfide or cadmium sulfides (CuS or CdS). These alternative hybrid materials were thoroughly built in past years to target research fields of strong impact, such as solar energy conversion, water splitting, environmental chemistry, or nanomedicine. Herein, we evaluate the influence of tuning the morphologies of the plasmonic gold nanostructures or the semiconductor interacting structures, and how these variations in geometry, either individual or combined, have a significant influence on the final photocatalytic performance

High-radiance LED-driven fluidized bed photoreactor for the complete oxidation of n-hexane in air

This work presents a highly efficient photo-reactor configuration for VOC abatement. It consists of a fluidized bed made of commercial, easy to fluidize, transparent borosilicate glass beads coated with commercial TiO2 nanoparticles (0.15–2.3 wt% loadings). Herein, we demonstrate that the use of high-radiance/low consumption UV-LEDs as irradiation sources with a deeper light penetration under fluidizing conditions facilitates the photocatalytic response to achieve the complete oxidation of VOCs. The role of different parameters such as catalyst loading and irradiation power have been thoroughly studied and evaluated to maximize the full combustion of n-hexane. Under the high radiance (up to 2200 mW/cm2) conditions used the bed heats significantly (up to 190 °C), although this did not have an effect on the conversions reached, which depended solely on the wavelength and power used. The productivity of the photoreactor tested and the space velocity used were around 5.25 × 10-2 mol/g·h and 12000 h-1 respectively

A note on "Convergence radius of Osada s method under Hölder continuous condition"

[EN] In this paper we revise the proofs of the results obtained in "Convergence radius of Osada's method under Holder continuous condition"[4], because the remainder of the Taylor's expansion used for the obtainment of the local convergence radius is not correct. So we perform the complete study in order to modify the equation for getting the local convergence radius, the uniqueness radius and the error bounds. Moreover a dynamical study for the third order Osada's method is also developed. (C) 2017 Elsevier Inc. All rights reserved.Hueso, J.; Martínez Molada, E.; Gupta, D.; Cevallos-Alarcon, FA. (2018). A note on "Convergence radius of Osada s method under Hölder continuous condition". Applied Mathematics and Computation. 321:689-699. https://doi.org/10.1016/j.amc.2017.11.003S68969932

Escaping undesired gas-phase chemistry: Microwave-driven selectivity enhancement in heterogeneous catalytic reactors

Research in solid-gas heterogeneous catalytic processes is typically aimed toward optimization of catalyst composition to achieve a higher conversion and, especially, a higher selectivity. However, even with the most selective catalysts, an upper limit is found: Above a certain temperature, gas-phase reactions become important and their effects cannot be neglected. Here, we apply a microwave field to a catalyst-support ensemble capable of direct microwave heating (MWH). We have taken extra precautions to ensure that (i) the solid phase is free from significant hot spots and (ii) an accurate estimation of both solid and gas temperatures is obtained. MWH allows operating with a catalyst that is significantly hotter than the surrounding gas, achieving a high conversion on the catalyst while reducing undesired homogeneous reactions. We demonstrate the concept with the CO 2 -mediated oxidative dehydrogenation of isobutane, but it can be applied to any system with significant undesired homogeneous contributions

Facile production of stable silicon nanoparticles: laser chemistry coupled to in situ stabilization via room temperature hydrosilylation

Stable, alkyl-terminated, light-emitting silicon nanoparticles have been synthesized in a continuous process by laser pyrolysis of a liquid trialkyl-silane precursor selected as a safer alternative to gas silane (SiH4). Stabilization was achieved by in situ reaction using a liquid collection system instead of the usual solid state filtration. The alkene contained in the collection liquid (1-dodecene) reacted with the newly formed silicon nanoparticles in an unusual room-temperature hydrosilylation process. It was achieved by the presence of fluoride species, also produced during laser pyrolysis from the decomposition of sulfur hexafluoride (SF6) selected as a laser sensitizer. This process directly rendered alkyl-passivated silicon nanoparticles with consistent morphology and size (<3 nm), avoiding the use of costly post-synthetic treatments

Upconverting Carbon Nanodots from EDTA as Near-Infrared Activated Phototheranostic Agents

This work describes the synthesis of nitrogen-doped carbon nanodots (CNDs) synthesized from ethylene diamine tetra acetic acid (EDTA) as a precursor and their application as luminescent agents with a dual-mode theranostic role as near-infrared (NIR) triggered imaging and photodynamic therapy agents. Interestingly, these fluorescent CNDs are more rapidly and selectively internalized in tumor cells and exhibit no cytotoxicity until remotely activated with a NIR illumination source. These CNDs are excellent candidates for photo-theranostic purposes, i.e.: simultaneous imaging and therapy can be carried out on cancer cells using their luminescent properties and the in situ generation of reactive oxidative species (ROS) upon excitation in the NIR range. In the presence of CNDs NIR remote activation induces the in vitro killing of U251 MG cells. Through the use of flow imaging cytometry we have been able to successfully map and quantify the different type of cell deaths induced by the presence of intracellular superoxide anions (¿O2-) and hydrogen peroxide (H2O2) ROS species generated in situ upon NIR irradiation

From bench scale to pilot plant: A 150x scaled-up configuration of a microwave-driven structured reactor for methane dehydroaromatization

Microwave-assisted gas-phase conversion on structured catalysts is emerging as a promising process intensifi-cation technology in the field of heterogeneous catalysis. The combination of selective heating and structured catalytic materials induces a temperature difference between the heated catalytic sample and the surrounding void regions to avoid non-selective gas-phase reactions. This operational principle allowed inhibiting thermal cracking in alkane dehydrogenation processes as well as retarding catalyst deactivation by coking in methane dehydroaromatization (MDA) processes. However, its effectiveness has not been reported so far out of the lab-oratory scale conditions. This work addresses the scaling of the microwave-assisted MDA process from lab scale experiments to a scaled-up configuration capable of stable operation with a 150-fold higher feeding rate. The scaling-up potential and main obstacles to overcome for this technology are critically discussed. In addition, a techno-economic assessment of the MW-MDA process is presented. The catalytic activity was kept for seven consecutive reaction cycles, i.e. 35 h MW-MDA, prior to a progressive decay due to permanent deactivation caused by zeolite dealumination and active metal loss. The scaled set-up operated for up to 295 consecutive hours under unmanned operation conducting 4 -h MDA-regeneration cycles on Mo/ZSM-5@SiC monoliths and resulting in 125-fold increase of converted methane and a 450-fold increase of benzene (0.17 LC6H6/h) in comparison with the laboratory scale tests. Scaled set-up experiments were run using only a 6-fold microwave input power, thus, highlighting the non-linearity between energy consumption and scaling factor for this tech-nology and the importance of microwave cavity design

Laser-driven direct synthesis of carbon nanodots and application as sensitizers for visible-light photocatalysis

We present the first successful synthesis of monodisperse carbon nanodots (CNDs) with tunable photoluminescence (PL) carried out by laser pyrolysis of two common volatile organic precursors such as toluene and pyridine. Remarkably, the initial chemical composition of the precursor determines the formation of undoped or N-doped CNDs and their corresponding absorption response in the visible range (expanded for the latter). We demonstrate the control and versatility of this synthesis method to tune the final outcome and its potential to explore a great number of potential solvent candidates. Furthermore, we have successfully exploited these CNDs (both undoped and N-doped) as effective sensitizers of TiO2 nanoparticles in the visible-light driven photo-degradation of a cationic dye selected as model organic pollutant