Instituto de Catálisis y Petroleoquímica

We present cosmological results from the final galaxy clustering data set of the Baryon Oscillation Spectroscopic Survey, part of the Sloan Digital Sky Survey III. Our combined galaxy sample comprises 1.2 million massive galaxies over an effective area of 9329 deg 2 and volume of 18.7 Gpc 3 , divided into three partially overlapping redshift slices centred at effective redshifts 0.38, 0.51 and 0.61. We measure the angular diameter distance D M and Hubble parameter H from the baryon acoustic oscillation (BAO) method, in combination with a cosmic microwave background prior on the sound horizon scale, after applying reconstruction to reduce non-linear effects on the BAO feature. Using the anisotropic clustering of the

Hydrogen peroxide (H2O2) is widely used in almost all industrial areas, particularly in the chemical industry and environmental protection. The only degradation product of its use is water, and thus it has played a large role in environmentally friendly methods in the chemical industry. Hydrogen peroxide is produced on an industrial scale by the anthraquinone oxidation (AO) process. However, this process can hardly be considered a green method. It involves the sequential hydrogenation and oxidation of an alkylanthraquinone precursor dissolved in a mixture of organic solvents followed by liquid-liquid extraction to recover H2O2. The AO process is a multistep method that requires significant energy input and generates waste, which has a negative effect on its sustainability and production costs. The transport, storage, and handling of bulk H2O2 involve hazards and escalating expenses. Thus, novel, cleaner methods for the production of H2O2 are being explored. The direct synthesis of H2O2 from O2 and H2 using a variety of catalysts, and the factors influencing the formation and decomposition of H2O2 are examined in detail in this Review.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTChemical Structures and Performance of Perovskite OxidesM. A. Peña and J. L. G. FierroView Author Information Instituto de Catalisis y Petroleoquimica, CSIC, Cantoblanco, 28049 Madrid, Spain Cite this: Chem. Rev. 2001, 101, 7, 1981–2018Publication Date (Web):May 31, 2001Publication History Received28 September 2000Published online31 May 2001Published inissue 1 July 2001https://pubs.acs.org/doi/10.1021/cr980129fhttps://doi.org/10.1021/cr980129fresearch-articleACS PublicationsCopyright © 2001 American Chemical SocietyRequest reuse permissionsArticle Views32611Altmetric-Citations2264LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Ions,Oxides,Oxygen,Perovskites,Redox reactions Get e-Alerts

Living species are continuously subjected to all extrinsic forms of reactive oxidants and others that are produced endogenously. There is extensive literature on the generation and effects of reactive oxygen species (ROS) in biological processes, both in terms of alteration and their role in cellular signaling and regulatory pathways. Cells produce ROS as a controlled physiological process, but increasing ROS becomes pathological and leads to oxidative stress and disease. The induction of oxidative stress is an imbalance between the production of radical species and the antioxidant defense systems, which can cause damage to cellular biomolecules, including lipids, proteins and DNA. Cellular and biochemical experiments have been complemented in various ways to explain the biological chemistry of ROS oxidants. However, it is often unclear how this translates into chemical reactions involving redox changes. This review addresses this question and includes a robust mechanistic explanation of the chemical reactions of ROS and oxidative stress.

Citation: Alam, S., Albareti, F. D., Prieto, C. A., Anders, F., Anderson, S. F., Anderton, T., . . . Zhu, G. T. (2015). THE ELEVENTH AND TWELFTH DATA RELEASES OF THE SLOAN DIGITAL SKY SURVEY: FINAL DATA FROM SDSS-III. Astrophysical Journal Supplement Series, 219(1), 27. doi:10.1088/0067-0049/219/1/12

Advanced nanostructured materials that demonstrate useful activity under solar excitation in fields concerned with the elimination of pollutants, partial oxidation and the valorization of chemical compounds, water splitting and CO 2 reduction processes, are discussed. Point defects present in nanoparticulated anatase present both 5-fold- and 6-fold-coordinated titanium atoms, as well as 2-fold- and 3-fold-coordinated oxygens. The requirement of using sunlight as the excitation source for the degradation reaction demands, as a principal requirement, the modification of the electronic characteristics of a UV absorber system such as anatase-TiO 2. Some reports also indicate the need for large doping concentrations for N-doping in specific cases where notable changes in the valence band onset are subsequently observed. The effect of cetyltrimethylammonium bromide (CTAB) on the crystallization is reported by Yin et al. They showed that the presence of CTAB induces the appearance of BiOBr during the synthesis at 80°C using an aqueous method.

Immobilization of enzymes may produce alterations in their observed activity, specificity or selectivity. Although in many cases an impoverishment of the enzyme properties is observed upon immobilization (caused by the distortion of the enzyme due to the interaction with the support) in some instances such properties may be enhanced by this immobilization. These alterations in enzyme properties are sometimes associated with changes in the enzyme structure. Occasionally, these variations will be positive. For example, they may be related to the stabilization of a hyperactivated form of the enzyme, like in the case of lipases immobilized on hydrophobic supports via interfacial activation. In some other instances, these improvements will be just a consequence of random modifications in the enzyme properties that in some reactions will be positive while in others may be negative. For this reason, the preparation of a library of biocatalysts as broad as possible may be a key turning point to find an immobilized biocatalyst with improved properties when compared to the free enzyme. Immobilized enzymes will be dispersed on the support surface and aggregation will no longer be possible, while the free enzyme may suffer aggregation, which greatly decreases enzyme activity. Moreover, enzyme rigidification may lead to preservation of the enzyme properties under drastic conditions in which the enzyme tends to become distorted thus decreasing its activity. Furthermore, immobilization of enzymes on a support, mainly on a porous support, may in many cases also have a positive impact on the observed enzyme behavior, not really related to structural changes. For example, the promotion of diffusional problems (e.g., pH gradients, substrate or product gradients), partition (towards or away from the enzyme environment, for substrate or products), or the blocking of some areas (e.g., reducing inhibitions) may greatly improve enzyme performance. Thus, in this tutorial review, we will try to list and explain some of the main reasons that may produce an improvement in enzyme activity, specificity or selectivity, either real or apparent, due to immobilization.

Abstract Enzyme biocatalysis plays a very relevant role in the development of many chemical industries, e.g., energy, food or fine chemistry. To achieve this goal, enzyme immobilization is a usual pre‐requisite as a solution to get reusable biocatalysts and thus decrease the price of this relatively expensive compound. However, a proper immobilization technique may permit far more than to get a reusable enzyme; it may be used to improve enzyme performance by improving some enzyme limitations: enzyme purity, stability (including the possibility of enzyme reactivation), activity, specificity, selectivity, or inhibitions. Among the diverse immobilization techniques, the use of pre‐existing supports to immobilize enzymes (via covalent or physical coupling) and the immobilization without supports [enzyme crosslinked aggregates (CLEAs) or crystals (CLECs)] are the most used or promising ones. This paper intends to give the advantages and disadvantages of the different existing immobilization strategies to solve the different aforementioned enzyme limitations. Moreover, the use of nanoparticles as immobilization supports is achieving an increasing importance, as the nanoparticles versatility increases and becomes more accessible to the researchers. We will also discuss here some of the advantages and drawbacks of these non porous supports compared to conventional porous supports. Although there are no universal optimal solutions for all cases, we will try to give some advice to select the optimal strategy for each particular enzyme and process, considering the enzyme properties, nature of the process and of the substrate. In some occasions the selection will be compulsory, for example due to the nature of the substrate. In other cases the optimal biocatalyst may depend on the company requirements (e.g., volumetric activity, enzyme stability, etc).

The aim of this review is to discuss the most relevant chemical routes for converting furfural to chemicals and to biofuels and additives.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTHydrogen Production Reactions from Carbon Feedstocks: Fossil Fuels and BiomassR. M. Navarro, M. A. Peña, and J. L. G. FierroView Author Information Instituto de Catalisis y Petroleoquimica, CSIC, Cantoblanco, 28049 Madrid, Spain Cite this: Chem. Rev. 2007, 107, 10, 3952–3991Publication Date (Web):August 23, 2007Publication History Received1 December 2006Published online23 August 2007Published inissue 1 October 2007https://pubs.acs.org/doi/10.1021/cr0501994https://doi.org/10.1021/cr0501994research-articleACS PublicationsCopyright © 2007 American Chemical SocietyRequest reuse permissionsArticle Views14483Altmetric-Citations1056LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Catalysts,Hydrocarbons,Hydrogen,Metals,Water Get e-Alerts

The spider mite Tetranychus urticae is a cosmopolitan agricultural pest with an extensive host plant range and an extreme record of pesticide resistance. Here we present the completely sequenced and annotated spider mite genome, representing the first complete chelicerate genome. At 90 megabases T. urticae has the smallest sequenced arthropod genome. Compared with other arthropods, the spider mite genome shows unique changes in the hormonal environment and organization of the Hox complex, and also reveals evolutionary innovation of silk production. We find strong signatures of polyphagy and detoxification in gene families associated with feeding on different hosts and in new gene families acquired by lateral gene transfer. Deep transcriptome analysis of mites feeding on different plants shows how this pest responds to a changing host environment. The T. urticae genome thus offers new insights into arthropod evolution and plant–herbivore interactions, and provides unique opportunities for developing novel plant protection strategies. The genome of the spider mite Tetranychus urticae is sequenced, providing insights into its polyphagous feeding, silk production, hormonal repertoire and reduced Hox cluster. The spider mite (Tetranychus urticae) is a common agricultural pest that feeds on a wide range of hosts — including maize (corn), soya, tomatoes and peppers — and is notoriously resistant to pesticides. Its genome has now been sequenced and analysed, providing insights into its hormonal repertoire and the evolution of silk production. Transcriptome analysis of mites feeding on different plants reveals how this pest defends itself in a changing host environment and gives pointers to possible non-pesticide plant-protection strategies. The genome encodes 17 fibroin genes, and physical tests of spider-mite silk show it to be a natural nanomaterial with fibres that are more than 100 times thinner than those produced by silk spiders.

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTNanostructured Oxides in Chemistry: Characterization and PropertiesM. Fernández-García, A. Martínez-Arias, J. C. Hanson, and J. A. RodriguezView Author Information Instituto de Catálisis y Petroleoquímica, CSIC, C/ Marie Curie s/n, Campus Cantoblanco, 28049-Madrid, Spain, and Brookhaven National Laboratory, Chemistry Department, Building 555, Upton, New York 11973 Cite this: Chem. Rev. 2004, 104, 9, 4063–4104Publication Date (Web):August 19, 2004Publication History Received22 December 2003Published online19 August 2004Published inissue 1 September 2004https://pubs.acs.org/doi/10.1021/cr030032fhttps://doi.org/10.1021/cr030032fresearch-articleACS PublicationsCopyright © 2004 American Chemical SocietyRequest reuse permissionsArticle Views10550Altmetric-Citations866LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Electrical conductivity,Metal oxide nanoparticles,Nanoparticles,Oxides,Particle size Get e-Alerts

ABSTRACT In a six-year program started in 2014 July, the Extended Baryon Oscillation Spectroscopic Survey (eBOSS) will conduct novel cosmological observations using the BOSS spectrograph at Apache Point Observatory. These observations will be conducted simultaneously with the Time Domain Spectroscopic Survey (TDSS) designed for variability studies and the Spectroscopic Identification of eROSITA Sources (SPIDERS) program designed for studies of X-ray sources. In particular, eBOSS will measure with percent-level precision the distance-redshift relation with baryon acoustic oscillations (BAO) in the clustering of matter. eBOSS will use four different tracers of the underlying matter density field to vastly expand the volume covered by BOSS and map the large-scale-structures over the relatively unconstrained redshift range 0.6 < z < 2.2. Using more than 250,000 new, spectroscopically confirmed luminous red galaxies at a median redshift z = 0.72, we project that eBOSS will yield measurements of the angular diameter distance d A ( z ) to an accuracy of 1.2% and measurements of H ( z ) to 2.1% when combined with the z > 0.6 sample of BOSS galaxies. With ∼195,000 new emission line galaxy redshifts, we expect BAO measurements of d A ( z ) to an accuracy of 3.1% and H ( z ) to 4.7% at an effective redshift of z = 0.87. A sample of more than 500,000 spectroscopically confirmed quasars will provide the first BAO distance measurements over the redshift range 0.9 < z < 2.2, with expected precision of 2.8% and 4.2% on d A ( z ) and H ( z ), respectively. Finally, with 60,000 new quasars and re-observation of 60,000 BOSS quasars, we will obtain new Ly α forest measurements at redshifts z > 2.1; these new data will enhance the precision of d A ( z ) and H ( z ) at z > 2.1 by a factor of 1.44 relative to BOSS. Furthermore, eBOSS will provide improved tests of General Relativity on cosmological scales through redshift-space distortion measurements, improved tests for non-Gaussianity in the primordial density field, and new constraints on the summed mass of all neutrino species. Here, we provide an overview of the cosmological goals, spectroscopic target sample, demonstration of spectral quality from early data, and projected cosmological constraints from eBOSS.

We review lattice results related to pion, kaon, [Formula: see text]- and [Formula: see text]-meson physics with the aim of making them easily accessible to the particle-physics community. More specifically, we report on the determination of the light-quark masses, the form factor [Formula: see text], arising in semileptonic [Formula: see text] transition at zero momentum transfer, as well as the decay-constant ratio [Formula: see text] of decay constants and its consequences for the CKM matrix elements [Formula: see text] and [Formula: see text]. Furthermore, we describe the results obtained on the lattice for some of the low-energy constants of [Formula: see text] and [Formula: see text] Chiral Perturbation Theory and review the determination of the [Formula: see text] parameter of neutral kaon mixing. The inclusion of heavy-quark quantities significantly expands the FLAG scope with respect to the previous review. Therefore, we focus here on [Formula: see text]- and [Formula: see text]-meson decay constants, form factors, and mixing parameters, since these are most relevant for the determination of CKM matrix elements and the global CKM unitarity-triangle fit. In addition we review the status of lattice determinations of the strong coupling constant [Formula: see text].

Chemical-looping combustion (CLC) has been suggested as an energetically efficient method for capture of carbon dioxide from the combustion of fuel gas. This technique involves the use of an oxygen carrier that transfers oxygen from the air to the fuel, preventing direct contact between them. The oxygen carrier is composed of a metal oxide as an oxygen source, and an inert as a binder for increasing the mechanical strength of the carrier. In this work, 240 samples composed of 40−80% of Cu, Fe, Mn, or Ni oxides on Al2O3, sepiolite, SiO2, TiO2, or ZrO2 were prepared by mechanical mixing as cylindrical extrudates. The samples were sintered at four temperatures between 950 and 1300 °C. The effects of the chemical nature and composition of the carrier and the sintering temperature were investigated by reactivity tests in a thermogravimetric analyzer using CH4 as fuel, and the mechanical strength of the solids. On the basis of these properties, the most promising carriers to be used in a CLC system were selected. The best Cu-based oxygen carriers were those prepared using SiO2 or TiO2 as inert, and sintered at 950 °C. Among the Fe-based oxygen carriers, those prepared with Al2O3 and ZrO2 as inerts showed the best behavior. ZrO2 was the best inert for those Mn-based oxygen carriers. Finally, TiO2 was the best inert for those Ni-based oxygen carriers.

OBJECTIVE: Antibiotic (AB) usage strongly affects microbial intestinal metabolism and thereby impacts human health. Understanding this process and the underlying mechanisms remains a major research goal. Accordingly, we conducted the first comparative omic investigation of gut microbial communities in faecal samples taken at multiple time points from an individual subjected to β-lactam therapy. METHODS: The total (16S rDNA) and active (16S rRNA) microbiota, metagenome, metatranscriptome (mRNAs), metametabolome (high-performance liquid chromatography coupled to electrospray ionisation and quadrupole time-of-flight mass spectrometry) and metaproteome (ultra high performing liquid chromatography coupled to an Orbitrap MS(2) instrument [UPLC-LTQ Orbitrap-MS/MS]) of a patient undergoing AB therapy for 14 days were evaluated. RESULTS: Apparently oscillatory population dynamics were observed, with an early reduction in Gram-negative organisms (day 6) and an overall collapse in diversity and possible further colonisation by 'presumptive' naturally resistant bacteria (day 11), followed by the re-growth of Gram-positive species (day 14). During this process, the maximum imbalance in the active microbial fraction occurred later (day 14) than the greatest change in the total microbial fraction, which reached a minimum biodiversity and richness on day 11; additionally, major metabolic changes occurred at day 6. Gut bacteria respond to ABs early by activating systems to avoid the antimicrobial effects of the drugs, while 'presumptively' attenuating their overall energetic metabolic status and the capacity to transport and metabolise bile acid, cholesterol, hormones and vitamins; host-microbial interactions significantly improved after treatment cessation. CONCLUSIONS: This proof-of-concept study provides an extensive description of gut microbiota responses to follow-up β-lactam therapy. The results demonstrate that ABs targeting specific pathogenic infections and diseases may alter gut microbial ecology and interactions with host metabolism at a much higher level than previously assumed.

Among renewable energies, wind and solar are inherently intermittent and therefore both require efficient energy storage systems to facilitate a round-the-clock electricity production at a global scale. In this context, concentrated solar power (CSP) stands out among other sustainable technologies because it offers the interesting possibility of storing energy collected from the sun as heat by sensible, latent, or thermochemical means. Accordingly, continuous electricity generation in the power block is possible even during off-sun periods, providing CSP plants with a remarkable dispatchability. Sensible heat storage has been already incorporated to commercial CSP plants. However, because of its potentially higher energy storage density, thermochemical heat storage (TCS) systems emerge as an attractive alternative for the design of next-generation power plants, which are expected to operate at higher temperatures. Through these systems, thermal energy is used to drive endothermic chemical reactions, which can subsequently release the stored energy when needed through a reversible exothermic step. This review analyzes the status of this prominent energy storage technology, its major challenges, and future perspectives, covering in detail the numerous strategies proposed for the improvement of materials and thermochemical reactors. Thermodynamic calculations allow selecting high energy density systems, but experimental findings indicate that sufficiently rapid kinetics and long-term stability trough continuous cycles of chemical transformation are also necessary for practical implementation. In addition, selecting easy-to-handle materials with reduced cost and limited toxicity is crucial for large-scale deployment of this technology. In this work, the possible utilization of materials as diverse as metal hydrides, hydroxides, or carbonates for thermochemical storage is discussed. Furthermore, special attention is paid to the development of redox metal oxides, such as Co3O4/CoO, Mn2O3/Mn3O4, and perovskites of different compositions, as an auspicious new class of TCS materials due to the advantage of working with atmospheric air as reactant, avoiding the need of gas storage tanks. Current knowledge about the structural, morphological, and chemical modifications of these solids, either caused during redox transformations or induced wittingly as a way to improve their properties, is revised in detail. In addition, the design of new reactor concepts proposed for the most efficient use of TCS in concentrated solar facilities is also critically considered. Finally, strategies for the harmonic integration of these units in functioning solar power plants as well as the economic aspects are also briefly assessed.

Abstract Splitting image : Sustainable hydrogen production is a key target for the development of alternative, future energy systems that will provide a clean and affordable energy supply. This Minireview focuses on the development of semiconductor catalysts that enable hydrogen production via water splitting upon visible‐light irradiation. magnified image Sustainable hydrogen production is a key target for the development of alternative, future energy systems that will provide a clean and affordable energy supply. The Sun is a source of silent and precious energy that is distributed fairly all over the Earth daily. However, its tremendous potential as a clean, safe, and economical energy source cannot be exploited unless the energy is accumulated or converted into more useful forms. The conversion of solar energy into hydrogen via the water‐splitting process, assisted by photo‐semiconductor catalysts, is one of the most promising technologies for the future because large quantities of hydrogen can potentially be generated in a clean and sustainable manner. This Minireview provides an overview of the principles, approaches, and research progress on solar hydrogen production via the water‐splitting reaction on photo‐semiconductor catalysts. It presents a survey of the advances made over the last decades in the development of catalysts for photochemical water splitting under visible‐light irradiation. The Minireview also analyzes the energy requirements and main factors that determine the activity of photocatalysts in the conversion of water into hydrogen and oxygen using sunlight. Remarkable progress has been made since the pioneering work by Fujishima and Honda in 1972, but he development of photocatalysts with improved efficiencies for hydrogen production from water using solar energy still faces major challenges. Research strategies and approaches adopted in the search for active and efficient photocatalysts, for example through new materials and synthesis methods, are presented and analyzed.

Raman spectra of graphene oxides (GOs) with different chemical compositions and synthesized by oxidation of distinct starting materials were analyzed to relate the spectral features to structural properties. The chemical compositions of different graphene oxides were determined by X-ray photoelectron spectroscopy (XPS), and nanoplatelets were characterized by zeta potential (ζ) and dynamic light scattering (DLS) measurements. The results indicated that the chemical composition, size, and superficial charge of the nanoplatelets depend on the starting material. We found five reported bands (D, D′, G, D″, and D*) in the first-order Raman spectrum and three bands (2D, D + D′, and 2D′) in the second-order Raman spectrum that successfully interpret the Raman spectra between 1000 and 3500 cm–1. Analysis of the bands allowed linear correlations to be found between the maximum positions of the 2D and D + D′ bands and between the relative intensities of the D and G bands (ID/IG) and the Csp2 percentage. Moreover, our results demonstrate that the relative intensities of the D′ and D bands are in excellent agreement with the theoretical correlations and allow the type of defects produced during oxidation, namely, vacancies or sp3 hybridation, to be related to the size of the graphene oxide sheets.

Laccases are multicopper containing enzymes capable of performing one electron oxidation of a broad range of substrates. Using molecular oxygen as the final electron acceptor, they release only water as a by-product, and as such, laccases are eco-friendly, versatile biocatalysts that have generated an enormous biotechnological interest. Indeed, this group of enzymes has been used in different industrial fields for very diverse purposes, from food additive and beverage processing to biomedical diagnosis, and as cross-linking agents for furniture construction or in the production of biofuels. Laccases have also been studied intensely in nanobiotechnology for the development of implantable biosensors and biofuel cells. Moreover, their capacity to transform complex xenobiotics makes them useful biocatalysts in enzymatic bioremediation. This review summarizes the most significant recent advances in the use of laccases and their future perspectives in biotechnology.