80 research outputs found

    Social Enterprise in Spain: A Diversity of Roots and a Proposal of Models

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    The term “social enterprise” was first used, at the end of the 1980s, by organisations that promoted the social and labour integration of persons at risk of social and labour exclusion and other similar social activities. The social economy sector has since slowly introduced this term to describe its entities in order to gain recognition by society, and it is working to promote a generally accepted definition of social enterprise’s behaviour based on the principles and values of the social economy (participation, general interest...). According to Article 5 of Spanish Law 5/2011 on the Social Economy, work integration social enterprises and so-called “special employment centres” are part of the social economy, and so are all firms and entities carrying out activities following the values and principles of the social economy sector. In this context, organisations of the social economy sector also are beginning to use the “social enterprise” concept. In Spain, a debate still exists regarding its exact definition. A mix of perspectives on this concept, with different nuances, can be observed. Besides, the current context of reduced governmental budgets and social services in Spain causes social organisations to adopt new approaches to this term of social enterprise, as this type of organisation is more likely to receive funds from the European Union. This paper’s objective is to analyse all perspectives on the concept of social enterprise as well as the various social enterprise models existing in Spain. The document structure is organized as follow. In the first section, we present the context and the main concepts related to social enterprises in this country. In the second section, we provide an analysis of changes in the evolution of social enterprise criteria to identify established models and emerging patterns. In the third section, we put forward another typology, based on institutionalisation stages. Finally, we conclude by recommending an approach to future work and provide a basic bibliography on the subject

    Electrochemical synthesis of peroxomonophosphate using boron-doped diamond anodes

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    A new method for the synthesis of peroxomonophosphate, based on the use of boron-doped diamond electrodes, is described. The amount of oxidant electrogenerated depends on the characteristics of the supporting media (pH and solute concentration) and on the operating conditions (temperature and current density). Results show that the pH, between values of 1 and 5, does not influence either the electrosynthesis of peroxomonophosphate or the chemical stability of the oxidant generated. Conversely, low temperatures are required during the electrosynthesis process to minimize the thermal decomposition of peroxomonophosphate and to guarantee significant oxidant concentration. In addition, a marked influence of both the current density and the initial substrate is observed. This observation can be explained in terms of the contribution of hydroxyl radicals in the oxidation mechanisms that occur on diamond surfaces. In the assays carried out below the water oxidation potential, the generation of hydroxyl radicals did not take place. In these cases, peroxomonophosphate generation occurs through a direct electron transfer and, therefore, at these low current densities lower concentrations are obtained. On the other hand, at higher potentials both direct and hydroxyl radical-mediated mechanisms contribute to the oxidant generation and the process is more efficient. In the same way, the contribution of hydroxyl radicals may also help to explain the significant influence of the substrate concentration. Thus, the coexistence of both phosphate and hydroxyl radicals is required to ensure the generation of significant amounts of peroxomonophosphoric acid

    Performance of Ti/Pt and Nb/BDD anodes for dechlorination of nitric acid and regeneration of silver(II) in a tubular reactor for the treatment of solid wastes in nuclear industry

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    One of the problems frequently encountered in the processing of nuclear fuels is the recovery of plutonium contained in various solid wastes. The difficulty is to make soluble the plutonium present as the refractory oxide PuO2. The dissolution of this oxide in nitric acid solutions is easily performed by means of silver(II) a strong oxidizing agent which is usually electrochemically generated on a platinum anode. However, certain solid residues that must be treated to separate actinides contain important quantities of chloride ions that require after dissolution in nitric acid a preliminary electrochemical step to be removed before introducing Ag(I) for Ag(II) electrogeneration. Research is conducted to find electrocatalytic materials being able to replace massive platinum in view to limit capital costs. In the present work a set-up including a two-compartment tubular reactor with recirculation of electrolytes was tested with anodes made of boron doped diamond coated niobium (Nb/BDD) and platinum coated titanium (Ti/Pt) grids for the removal of chlorides (up to 0.1 M) and for silver(II) regeneration. The study showed that these two anodes are effective for the removal of chlorides contained in 6 M HNO3 solution as gaseous chlorine, without producing the unwanted oxyanions of chlorine. Furthermore, the regeneration rate of silver(II) on Nb/BDD anode is approximately equal to that obtained on Ti/Pt anode for the same hydrodynamic conditions in the tubular reactor. Accordingly, dechlorination as well as silver(II) regeneration can be performed in the same reactor equipped either with a Nb/BDD or a Ti/Pt anode. Besides, the service life of Nb/BDD anodes estimated by accelerated life tests conducted in 6 M HNO3 can be considered as very satisfactory compared to that observed with Ti/Pt anodes

    Electrochemical treatment of industrial organic wastewaters

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    A review, with 29 refs., on the anodic oxidn. of orgs. in industrial wastewaters treatment. Direct electrochem. processes catalyzed by the O transfer reaction are discussed for several anode materials. Ti/SnO2 is particularly efficient for cold combustion of arom. pollutants. Processes involving the electrochem. generation of oxidants (O3, H2O2), or the electrochem. regeneration of metallic redox couples (Fenton's reagent) are discussed. [on SciFinder (R)

    Comparison of the chemical and electrochemical oxidation of phenol for wastewater

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    The electrochem. oxidn. of PhOH in wastewater was studied using Pt and DSA anodes. Anal. of reaction intermediates and measurements of current efficiency have shown that traditional anode materials (Pt, Ti/IrO2, Ti/RuO2, Ti/PbO2) give relatively low current efficiencies (EOI). Contrary to the Ti/SnO2 anode which not only gives high EOI values but allows quasi complete Total org. C elimination. The electrochem. oxidn. is compared with the chem. oxidn. and a mechanism for the electrochem. oxidn. is proposed. [on SciFinder (R)
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