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    <title>DSpace Community:</title>
    <link>http://hdl.handle.net/2117/3795</link>
    <description />
    <pubDate>Thu, 23 May 2013 07:46:12 GMT</pubDate>
    <dc:date>2013-05-23T07:46:12Z</dc:date>
    <itunes:owner>
      <itunes:email>webmaster.bupc@upc.edu</itunes:email>
      <itunes:name>Universitat Politècnica de Catalunya. Servei de Biblioteques i Documentació</itunes:name>
    </itunes:owner>
    <itunes:explicit>no</itunes:explicit>
    <itunes:keywords />
    <item>
      <title>Determination of fungicides in residual tanning floats using solid phase micro extraction</title>
      <link>http://hdl.handle.net/2117/17584</link>
      <description>Title: Determination of fungicides in residual tanning floats using solid phase micro extraction
Authors: Font Vallès, Joaquim; Reyes Reyes, Maria; Cuadros, Sara; Bacardit Dalmases, Anna; Ollé Otero, Lluís; Marsal Monge, Agustín
Abstract: Solid-phase microextraction (SPME) was optimized for extraction of the leather preservative agents 2-(thiocyanomethylthio)-benzothiazole (TCMTB), 4-chloro-3-methylphenol (PCMC), 2-phenylphenol (OPP), 2-Octyl-3(2H)-isothiazolone (OIT), 2-mercaptobenzothiazol (MBT) and 3-iodo-2-propynyl-butylcarbamate (IPBC) in spent tanning floats. Determination was carried out by high performance  liquid chromatography (HPLC) with photo diode array detection (PDA). The following parameters were studied to achieve the maximum efficiency in extraction: fiber type, adsorption conditions (extraction time, ionic strength, temperature) and desorption parameters (time, temperature and composition of the desorption solvent). Results indicate that SPME using a 60um polydimethylsiloxane/divinylbenzene (PDMS/DVB) fiber is appropriate for the extraction of these types of compounds. Recoveries ranged from 82% to 116% with RSDs between +-8% and +-12% and limits of detection below 1 mg/L except for IPBC. The optimized procedure was successfully applied for the determination of leather preservatives in eleven residual tanning floats taken from different companies. This method enables us to determine quantitatively the fungicides contained in th residual floats. Consequently, it will constitute a very useful tool to improve the preservative uptake in leather manufacturing processes</description>
      <pubDate>Tue, 05 Feb 2013 15:48:08 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/17584</guid>
      <dc:date>2013-02-05T15:48:08Z</dc:date>
      <itunes:author>Font Vallès, Joaquim; Reyes Reyes, Maria; Cuadros, Sara; Bacardit Dalmases, Anna; Ollé Otero, Lluís; Marsal Monge, Agustín</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>Solid-phase microextraction (SPME) was optimized for extraction of the leather preservative agents 2-(thiocyanomethylthio)-benzothiazole (TCMTB), 4-chloro-3-methylphenol (PCMC), 2-phenylphenol (OPP), 2-Octyl-3(2H)-isothiazolone (OIT), 2-mercaptobenzothiazol (MBT) and 3-iodo-2-propynyl-butylcarbamate (IPBC) in spent tanning floats. Determination was carried out by high performance  liquid chromatography (HPLC) with photo diode array detection (PDA). The following parameters were studied to achieve the maximum efficiency in extraction: fiber type, adsorption conditions (extraction time, ionic strength, temperature) and desorption parameters (time, temperature and composition of the desorption solvent). Results indicate that SPME using a 60um polydimethylsiloxane/divinylbenzene (PDMS/DVB) fiber is appropriate for the extraction of these types of compounds. Recoveries ranged from 82% to 116% with RSDs between +-8% and +-12% and limits of detection below 1 mg/L except for IPBC. The optimized procedure was successfully applied for the determination of leather preservatives in eleven residual tanning floats taken from different companies. This method enables us to determine quantitatively the fungicides contained in th residual floats. Consequently, it will constitute a very useful tool to improve the preservative uptake in leather manufacturing processes</itunes:summary>
    </item>
    <item>
      <title>Evaluation of a lime-mediated sewage sludge stabilisation process. Product characterisation and technological validation for its use in the cement industry</title>
      <link>http://hdl.handle.net/2117/16482</link>
      <description>Title: Evaluation of a lime-mediated sewage sludge stabilisation process. Product characterisation and technological validation for its use in the cement industry
Authors: Flores, J.; Larrotcha, E.; Fos, C.; Husillos Rodríguez, N.; Granados, R.J.; Blanco Varela, M.Teresa; Cortina Pallás, José Luís; Martínez Ramírez, Sagrario; Marsal Astort, Montserrat; Guillem, Manel; Puig, J.
Abstract: This paper describes an industrial process for stabilising sewage sludge (SS) with lime and evaluates the&#xD;
viability of the stabilised product, denominated Neutral, as a raw material for the cement industry. Lime&#xD;
not only stabilised the sludge, raised the temperature of the mix to 80–100  C, furthering water evaporation,&#xD;
portlandite formation and the partial oxidation of the organic matter present in the sludge.&#xD;
Process mass and energy balances were determined. Neutral, a white powder consisting of portlandite&#xD;
(49.8%), calcite (16.6%), inorganic oxides (13.4%) and organic matter and moisture (20.2%), proved to be&#xD;
technologically apt for inclusion as a component in cement raw mixes. In this study, it was used instead&#xD;
of limestone in raw mixes clinkerised at 1400, 1450 and 1500  C. These raw meals exhibited greater reactivity&#xD;
at high temperatures than the limestone product and their calcination at 1500  C yielded clinker&#xD;
containing over 75% calcium silicates, the key phases in Portland clinker. Finally, the two types of raw&#xD;
meal (Neutral and limestone) were observed to exhibit similar mineralogy and crystal size and&#xD;
distribution.</description>
      <pubDate>Fri, 14 Sep 2012 08:09:11 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/16482</guid>
      <dc:date>2012-09-14T08:09:11Z</dc:date>
      <itunes:author>Flores, J.; Larrotcha, E.; Fos, C.; Husillos Rodríguez, N.; Granados, R.J.; Blanco Varela, M.Teresa; Cortina Pallás, José Luís; Martínez Ramírez, Sagrario; Marsal Astort, Montserrat; Guillem, Manel; Puig, J.</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords>Alximix, Cement reuse, Clinker, Lime stabilisation, Neutral, Sewage sludge</itunes:keywords>
      <itunes:summary>This paper describes an industrial process for stabilising sewage sludge (SS) with lime and evaluates the&#xD;
viability of the stabilised product, denominated Neutral, as a raw material for the cement industry. Lime&#xD;
not only stabilised the sludge, raised the temperature of the mix to 80–100  C, furthering water evaporation,&#xD;
portlandite formation and the partial oxidation of the organic matter present in the sludge.&#xD;
Process mass and energy balances were determined. Neutral, a white powder consisting of portlandite&#xD;
(49.8%), calcite (16.6%), inorganic oxides (13.4%) and organic matter and moisture (20.2%), proved to be&#xD;
technologically apt for inclusion as a component in cement raw mixes. In this study, it was used instead&#xD;
of limestone in raw mixes clinkerised at 1400, 1450 and 1500  C. These raw meals exhibited greater reactivity&#xD;
at high temperatures than the limestone product and their calcination at 1500  C yielded clinker&#xD;
containing over 75% calcium silicates, the key phases in Portland clinker. Finally, the two types of raw&#xD;
meal (Neutral and limestone) were observed to exhibit similar mineralogy and crystal size and&#xD;
distribution.</itunes:summary>
    </item>
    <item>
      <title>Determinación de TCMTB y otros fungicidas en piel</title>
      <link>http://hdl.handle.net/2117/16427</link>
      <description>Title: Determinación de TCMTB y otros fungicidas en piel
Authors: Reyes Farrera, María R.; Font Vallès, Joaquim; Bacardit Dalmases, Anna; Marsal Monge, Agustín
Abstract: La norma ISO 13365:2011 desarrolla un método analítico para la determinación del contenido&#xD;
de los agentes conservantes 2-(tiocianometiltio)-benzotiazol (TCMTB), 4-cloro-3-metilfenol&#xD;
(PCMC), 2-fenilfenol (OPP) y 2-octil-3(2H)-isotiazolona (OIT) en cuero por cromatografía líquida.&#xD;
La determinación simultanea de los fungicidas TCMTB, PCMC, OPP, OIT, y también de 2-mercaptobenzothiazol (MBT) y 3-yodo-2-propinil-butilo (IPBC) en muestras de piel se llevó a cabo mediante cromatografía líquida (HPLC) con detector ultravioleta de fotodiodos (PDA). La preparación de la muestra y el proceso de extracción se realizaron siguiendo la norma&#xD;
ISO 13365. La fase móvil consistió en agua con un 0.1% de ácido fórmico (A) y acetonitrilo con un 0.1% de ácido fórmico (B). En la detección cromatográfica se introdujo un pequeño cambio en relación con la norma. Se utilizó un detector de fotodiodos en lugar de un detector&#xD;
de longitud de onda fija para mejorar la fiabilidad de las identificaciones y la sensibilidad de la cuantificación.&#xD;
Se ha comprobado que el 2,4,6-triclorofenol (TCP) y el pentaclorofenol (PCP) no interfieren en la determinación.&#xD;
Las fortificaciones de 30 y 300 mg/kg en cuero produjeron unas recuperaciones medias de TCMTB del 94% y 99%, respectivamente. Las recuperaciones de los otros fungicidas fueron&#xD;
similares. Los fungicidas investigados se determinaron en 40 muestras de cueros del&#xD;
mercado. En el 90% de las muestras se encontraron residuos de TCMTB.&#xD;
En resumen, la nueva norma ISO 13365:2011 proporciona un método rápido y fiable, no&#xD;
sólo para la determinación de las cuatro moléculas incluidas en el ámbito de aplicación de la norma, sino también para otros fungicidas como el IPBC y el MBT</description>
      <pubDate>Tue, 04 Sep 2012 16:42:12 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/16427</guid>
      <dc:date>2012-09-04T16:42:12Z</dc:date>
      <itunes:author>Reyes Farrera, María R.; Font Vallès, Joaquim; Bacardit Dalmases, Anna; Marsal Monge, Agustín</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>La norma ISO 13365:2011 desarrolla un método analítico para la determinación del contenido&#xD;
de los agentes conservantes 2-(tiocianometiltio)-benzotiazol (TCMTB), 4-cloro-3-metilfenol&#xD;
(PCMC), 2-fenilfenol (OPP) y 2-octil-3(2H)-isotiazolona (OIT) en cuero por cromatografía líquida.&#xD;
La determinación simultanea de los fungicidas TCMTB, PCMC, OPP, OIT, y también de 2-mercaptobenzothiazol (MBT) y 3-yodo-2-propinil-butilo (IPBC) en muestras de piel se llevó a cabo mediante cromatografía líquida (HPLC) con detector ultravioleta de fotodiodos (PDA). La preparación de la muestra y el proceso de extracción se realizaron siguiendo la norma&#xD;
ISO 13365. La fase móvil consistió en agua con un 0.1% de ácido fórmico (A) y acetonitrilo con un 0.1% de ácido fórmico (B). En la detección cromatográfica se introdujo un pequeño cambio en relación con la norma. Se utilizó un detector de fotodiodos en lugar de un detector&#xD;
de longitud de onda fija para mejorar la fiabilidad de las identificaciones y la sensibilidad de la cuantificación.&#xD;
Se ha comprobado que el 2,4,6-triclorofenol (TCP) y el pentaclorofenol (PCP) no interfieren en la determinación.&#xD;
Las fortificaciones de 30 y 300 mg/kg en cuero produjeron unas recuperaciones medias de TCMTB del 94% y 99%, respectivamente. Las recuperaciones de los otros fungicidas fueron&#xD;
similares. Los fungicidas investigados se determinaron en 40 muestras de cueros del&#xD;
mercado. En el 90% de las muestras se encontraron residuos de TCMTB.&#xD;
En resumen, la nueva norma ISO 13365:2011 proporciona un método rápido y fiable, no&#xD;
sólo para la determinación de las cuatro moléculas incluidas en el ámbito de aplicación de la norma, sino también para otros fungicidas como el IPBC y el MBT</itunes:summary>
    </item>
    <item>
      <title>SR-XRD and SR-FTIR study of the alteration of silver foils in medieval paintings</title>
      <link>http://hdl.handle.net/2117/16414</link>
      <description>Title: SR-XRD and SR-FTIR study of the alteration of silver foils in medieval paintings
Authors: Salvadó Cabré, Nativitat; Buti Papiol, Salvador; Labrador, A.; Cinque, Gianfelice; Emerich, Hermann; Pradell Cara, Trinitat
Abstract: Altarpieces and polychrome carved wood from&#xD;
the fifteenth century AD usually exhibit golden and&#xD;
silvery areas by the application of a very thin foil of&#xD;
metal. The metal foils were normally protected from the&#xD;
atmosphere by a varnish or resin which maybe either&#xD;
preserved or absent. Moreover, they were glued to the&#xD;
background surface by adhesive substances (egg yolk,&#xD;
drying oil or animal glue). The high proportion of the&#xD;
glueing substances often renders the development of&#xD;
reaction compounds. With time, silver alters blacken or&#xD;
simply disappear completely. In this paper, we study the&#xD;
alterations to metal foils from a selection of fifteenth&#xD;
century artworks showing different glueing agents,&#xD;
organic coatings and several degrees of conservation of&#xD;
the organic coatings and metal leafs. The submillimetric&#xD;
layered structure and the high variability and low&#xD;
amount of most of the compounds present in the&#xD;
different layers, as well as their differing nature (organic&#xD;
and inorganic) make the use of micron-sensitive highresolution&#xD;
techniques essential for their study. In particular,&#xD;
the high resolution, high brilliance and small footprint&#xD;
renders synchrotron radiation most adequate for their&#xD;
study. SR-XRD was performed to identify the reaction&#xD;
compounds formed in the different layers; μFTIR was&#xD;
used at to identify the silver protecting organic coatings,&#xD;
the metal foil glueing layers and the corresponding&#xD;
reaction compounds. The results obtained suggest that&#xD;
atmospheric corrosion is the dominant mechanism, and&#xD;
therefore that the degree of corrosion of the metal foils is&#xD;
mainly related to the conservation state of the protecting&#xD;
coatings.</description>
      <pubDate>Mon, 03 Sep 2012 08:12:52 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/16414</guid>
      <dc:date>2012-09-03T08:12:52Z</dc:date>
      <itunes:author>Salvadó Cabré, Nativitat; Buti Papiol, Salvador; Labrador, A.; Cinque, Gianfelice; Emerich, Hermann; Pradell Cara, Trinitat</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>Altarpieces and polychrome carved wood from&#xD;
the fifteenth century AD usually exhibit golden and&#xD;
silvery areas by the application of a very thin foil of&#xD;
metal. The metal foils were normally protected from the&#xD;
atmosphere by a varnish or resin which maybe either&#xD;
preserved or absent. Moreover, they were glued to the&#xD;
background surface by adhesive substances (egg yolk,&#xD;
drying oil or animal glue). The high proportion of the&#xD;
glueing substances often renders the development of&#xD;
reaction compounds. With time, silver alters blacken or&#xD;
simply disappear completely. In this paper, we study the&#xD;
alterations to metal foils from a selection of fifteenth&#xD;
century artworks showing different glueing agents,&#xD;
organic coatings and several degrees of conservation of&#xD;
the organic coatings and metal leafs. The submillimetric&#xD;
layered structure and the high variability and low&#xD;
amount of most of the compounds present in the&#xD;
different layers, as well as their differing nature (organic&#xD;
and inorganic) make the use of micron-sensitive highresolution&#xD;
techniques essential for their study. In particular,&#xD;
the high resolution, high brilliance and small footprint&#xD;
renders synchrotron radiation most adequate for their&#xD;
study. SR-XRD was performed to identify the reaction&#xD;
compounds formed in the different layers; μFTIR was&#xD;
used at to identify the silver protecting organic coatings,&#xD;
the metal foil glueing layers and the corresponding&#xD;
reaction compounds. The results obtained suggest that&#xD;
atmospheric corrosion is the dominant mechanism, and&#xD;
therefore that the degree of corrosion of the metal foils is&#xD;
mainly related to the conservation state of the protecting&#xD;
coatings.</itunes:summary>
    </item>
    <item>
      <title>Study of the effect of temperature, relative humidity and UV radiation on chrome-tanned leather ageing</title>
      <link>http://hdl.handle.net/2117/15982</link>
      <description>Title: Study of the effect of temperature, relative humidity and UV radiation on chrome-tanned leather ageing
Authors: Bacardit Dalmases, Anna; Jorba, Montse; Font Vallès, Joaquim; Ollé Otero, Lluís
Abstract: Since leather is strongly affected by three main environmental parameters: temperature, relative humidity and UV radiation, this piece of research focuses on the effect that these three factors have on chrome-tanned leather ageing. Chrome tanned leathers were exposed to weathering effects in a climatic chamber in order to identify the most important variables affecting this weathering process and also to check for any possible interactions. Both a multilevel centralized factorial experimental design and an analysis of variance (ANOVA) were used as statistical tools for estimating the effects of the parameters</description>
      <pubDate>Thu, 07 Jun 2012 15:37:22 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/15982</guid>
      <dc:date>2012-06-07T15:37:22Z</dc:date>
      <itunes:author>Bacardit Dalmases, Anna; Jorba, Montse; Font Vallès, Joaquim; Ollé Otero, Lluís</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>Since leather is strongly affected by three main environmental parameters: temperature, relative humidity and UV radiation, this piece of research focuses on the effect that these three factors have on chrome-tanned leather ageing. Chrome tanned leathers were exposed to weathering effects in a climatic chamber in order to identify the most important variables affecting this weathering process and also to check for any possible interactions. Both a multilevel centralized factorial experimental design and an analysis of variance (ANOVA) were used as statistical tools for estimating the effects of the parameters</itunes:summary>
    </item>
    <item>
      <title>Curtición vegetal con extracto de semilla de uva</title>
      <link>http://hdl.handle.net/2117/15919</link>
      <description>Title: Curtición vegetal con extracto de semilla de uva
Authors: Ramon Arcal, Salvador; Bacardit Dalmases, Anna; Font Vallès, Joaquim; Ollé Otero, Lluís
Abstract: El objetivo de este trabajo es estudiar la viabilidad de usar el extracto de semilla de&#xD;
uva procedente de subproductos de la industria vinícola, como fuente sostenible y&#xD;
renovable de taninos para curtir pieles vacunas al vegetal, frente a los extractos&#xD;
vegetales convencionales de quebracho, mimosa, castaño, gambier, o tara que&#xD;
provienen de arboles cultivados en zonas geográficas concretas. La substitución parcial en el proceso industrial de las tenerías de alguno de los extractos habituales por el de semilla de uva, contribuiría al esfuerzo por preservar la deforestación del planeta. Primero se comparan las características físicas de la piel vacuna curtida con un extracto único, para fabricar vaquetilla vegetal natural. Se evalúa el artículo obtenido y se controlan las resistencias a la tracción y al desgarro, alargamiento a la rotura,&#xD;
grueso, solidez a la luz, color y absorción de agua. También se realiza una cromatografía líquida de cada uno de los taninos usados. A continuación se realiza un “coupage” de extracto de semilla de uva con otros extractos comerciales para conseguir una vaquetilla con mejores prestaciones y se&#xD;
compara con productos comerciales presentes en el mercado de la marroquinería de&#xD;
alta calidad</description>
      <pubDate>Thu, 24 May 2012 11:40:05 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/15919</guid>
      <dc:date>2012-05-24T11:40:05Z</dc:date>
      <itunes:author>Ramon Arcal, Salvador; Bacardit Dalmases, Anna; Font Vallès, Joaquim; Ollé Otero, Lluís</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>El objetivo de este trabajo es estudiar la viabilidad de usar el extracto de semilla de&#xD;
uva procedente de subproductos de la industria vinícola, como fuente sostenible y&#xD;
renovable de taninos para curtir pieles vacunas al vegetal, frente a los extractos&#xD;
vegetales convencionales de quebracho, mimosa, castaño, gambier, o tara que&#xD;
provienen de arboles cultivados en zonas geográficas concretas. La substitución parcial en el proceso industrial de las tenerías de alguno de los extractos habituales por el de semilla de uva, contribuiría al esfuerzo por preservar la deforestación del planeta. Primero se comparan las características físicas de la piel vacuna curtida con un extracto único, para fabricar vaquetilla vegetal natural. Se evalúa el artículo obtenido y se controlan las resistencias a la tracción y al desgarro, alargamiento a la rotura,&#xD;
grueso, solidez a la luz, color y absorción de agua. También se realiza una cromatografía líquida de cada uno de los taninos usados. A continuación se realiza un “coupage” de extracto de semilla de uva con otros extractos comerciales para conseguir una vaquetilla con mejores prestaciones y se&#xD;
compara con productos comerciales presentes en el mercado de la marroquinería de&#xD;
alta calidad</itunes:summary>
    </item>
    <item>
      <title>Nuevas aplicaciones de la cromatografía iónica en el sector de curtidos</title>
      <link>http://hdl.handle.net/2117/15918</link>
      <description>Title: Nuevas aplicaciones de la cromatografía iónica en el sector de curtidos
Authors: Perez Quiñones, Carmen; Bacardit Dalmases, Anna; Ollé Otero, Lluís; Reyes Ferrera, Mª Reyes; Font Vallès, Joaquim
Abstract: La industria de curtidos utiliza gran variedad de productos químicos en las diferentes etapas del proceso de curtición. Una parte de estos productos son absorbidos por las pieles, mientras que el resto pasan a las aguas residuales contribuyendo algunos de ellos al aumento de la salinidad. Muchos de estos productos químicos presentan un componente aniónico. En el contexto del control de calidad, los laboratorios del sector de curtidos tienen la necesidad de analizar especies aniónicas en diferentes muestras, tales como productos químicos, aguas residuales, baños de diferentes etapas y piel piquelada, curtida y acabada.&#xD;
En otros sectores, la tendencia actual en el análisis de aniones es el uso de técnicas&#xD;
sensibles y rápidas, como la cromatografía líquida de alta resolución. En este estudio se desarrollan métodos cromatográficos innovadores, con detección ultravioleta indirecta y directa, para la determinación simultánea de los principales aniones&#xD;
de interés en la industria de curtidos (cloruro, sulfato, nitrato, acetato, formiato, fosfato, nitrato, fluoruro y bromuro). Estos métodos se aplican a diferentes muestras. Se optimiza un método con cromatografía iónica y detección indirecta. La separación se realiza utilizando biftalato potásico como fase móvil. También se presenta un nuevo método cromatográfico simple, con detección ultravioleta directa y sulfato sódico como eluyente</description>
      <pubDate>Thu, 24 May 2012 11:11:17 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/15918</guid>
      <dc:date>2012-05-24T11:11:17Z</dc:date>
      <itunes:author>Perez Quiñones, Carmen; Bacardit Dalmases, Anna; Ollé Otero, Lluís; Reyes Ferrera, Mª Reyes; Font Vallès, Joaquim</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>La industria de curtidos utiliza gran variedad de productos químicos en las diferentes etapas del proceso de curtición. Una parte de estos productos son absorbidos por las pieles, mientras que el resto pasan a las aguas residuales contribuyendo algunos de ellos al aumento de la salinidad. Muchos de estos productos químicos presentan un componente aniónico. En el contexto del control de calidad, los laboratorios del sector de curtidos tienen la necesidad de analizar especies aniónicas en diferentes muestras, tales como productos químicos, aguas residuales, baños de diferentes etapas y piel piquelada, curtida y acabada.&#xD;
En otros sectores, la tendencia actual en el análisis de aniones es el uso de técnicas&#xD;
sensibles y rápidas, como la cromatografía líquida de alta resolución. En este estudio se desarrollan métodos cromatográficos innovadores, con detección ultravioleta indirecta y directa, para la determinación simultánea de los principales aniones&#xD;
de interés en la industria de curtidos (cloruro, sulfato, nitrato, acetato, formiato, fosfato, nitrato, fluoruro y bromuro). Estos métodos se aplican a diferentes muestras. Se optimiza un método con cromatografía iónica y detección indirecta. La separación se realiza utilizando biftalato potásico como fase móvil. También se presenta un nuevo método cromatográfico simple, con detección ultravioleta directa y sulfato sódico como eluyente</itunes:summary>
    </item>
    <item>
      <title>Comparison of weathering variables on chrome-tanned and wet-white leather ageing</title>
      <link>http://hdl.handle.net/2117/15267</link>
      <description>Title: Comparison of weathering variables on chrome-tanned and wet-white leather ageing
Authors: Ollé Otero, Lluís; Jorba, Montse; Castell, Joan Carles; Font Vallès, Joaquim; Bacardit Dalmases, Anna
Abstract: Leather is a natural material that can be used in different environments and often under aggressive environmental conditions that may cause premature ageing. The most important factors influencing the degradation of leather are temperature, relative humidity and UV radiation. Leathers with chrome tannage and wet-white leathers were exposed to weathering effects using a climatic chamber in order to identify the most important variables affecting this weathering process and to check for interactions. Both a multilevel centralized factorial experimental design and an analysis of variance (ANOVA) have&#xD;
been employed as statistical tools for estimating the effects of the parameters</description>
      <pubDate>Tue, 21 Feb 2012 10:39:49 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/15267</guid>
      <dc:date>2012-02-21T10:39:49Z</dc:date>
      <itunes:author>Ollé Otero, Lluís; Jorba, Montse; Castell, Joan Carles; Font Vallès, Joaquim; Bacardit Dalmases, Anna</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>Leather is a natural material that can be used in different environments and often under aggressive environmental conditions that may cause premature ageing. The most important factors influencing the degradation of leather are temperature, relative humidity and UV radiation. Leathers with chrome tannage and wet-white leathers were exposed to weathering effects using a climatic chamber in order to identify the most important variables affecting this weathering process and to check for interactions. Both a multilevel centralized factorial experimental design and an analysis of variance (ANOVA) have&#xD;
been employed as statistical tools for estimating the effects of the parameters</itunes:summary>
    </item>
    <item>
      <title>Recovery of organic nitrogen from beamhouse wastewater in a hair recovery process</title>
      <link>http://hdl.handle.net/2117/13832</link>
      <description>Title: Recovery of organic nitrogen from beamhouse wastewater in a hair recovery process
Authors: Rius Carrasco, Antoni; Marsal Monge, Agustín; Bautista, E.; Cuadros, Sara; Reyes Reyes, Maria; Font Vallès, Joaquim
Abstract: In the leather industry, in addition to the extrinsic contamination attributable to chemical products not absorbed by the hides, there is intrinsic contamination produced by the hides themselves. From each 100kg of raw material, 15kg of solubilised protein will end up in wastewater in the early stages of the process of transforming hides into&#xD;
leather. These proteins contain nearly 18% of nitrogen. In this study it is proposed to recover organic nitrogen from the proteins present in the effluents of the beamhouse operations of hides and the subsequent revalorization of the protein fraction obtained. This work seeks to characterize (the chemical oxygen demand (COD), total nitrogen, ammonium nitrogen, total&#xD;
soluble nitrogen, particulate nitrogen, organic nitrogen and protein) the wastewaters, individually or in groups, of&#xD;
the various beamhouse operations (soaking, unhairing-liming, washing, conditioning, deliming, bating, washing and pickling) with hair recovery. The studies are presented of the determination of the pH value (adjusted by means of buffers of acetic acid/sodium acetate) at which the greatest precipitate of the protein fraction is produced. In addition, the following tests were performed to characterize these precipitates: determination of the quantitative composition&#xD;
of the main components of the protein fraction (humidity, proteins, free amino acids, fats and other matter soluble&#xD;
in dichloromethane and ash); heavy metals content, calcium, magnesium, potassium and sodium and the composition in total amino acids with prior acid hydrolysis of the protein fraction with 6N hydrochloric acid.</description>
      <pubDate>Wed, 09 Nov 2011 11:52:49 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/13832</guid>
      <dc:date>2011-11-09T11:52:49Z</dc:date>
      <itunes:author>Rius Carrasco, Antoni; Marsal Monge, Agustín; Bautista, E.; Cuadros, Sara; Reyes Reyes, Maria; Font Vallès, Joaquim</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>In the leather industry, in addition to the extrinsic contamination attributable to chemical products not absorbed by the hides, there is intrinsic contamination produced by the hides themselves. From each 100kg of raw material, 15kg of solubilised protein will end up in wastewater in the early stages of the process of transforming hides into&#xD;
leather. These proteins contain nearly 18% of nitrogen. In this study it is proposed to recover organic nitrogen from the proteins present in the effluents of the beamhouse operations of hides and the subsequent revalorization of the protein fraction obtained. This work seeks to characterize (the chemical oxygen demand (COD), total nitrogen, ammonium nitrogen, total&#xD;
soluble nitrogen, particulate nitrogen, organic nitrogen and protein) the wastewaters, individually or in groups, of&#xD;
the various beamhouse operations (soaking, unhairing-liming, washing, conditioning, deliming, bating, washing and pickling) with hair recovery. The studies are presented of the determination of the pH value (adjusted by means of buffers of acetic acid/sodium acetate) at which the greatest precipitate of the protein fraction is produced. In addition, the following tests were performed to characterize these precipitates: determination of the quantitative composition&#xD;
of the main components of the protein fraction (humidity, proteins, free amino acids, fats and other matter soluble&#xD;
in dichloromethane and ash); heavy metals content, calcium, magnesium, potassium and sodium and the composition in total amino acids with prior acid hydrolysis of the protein fraction with 6N hydrochloric acid.</itunes:summary>
    </item>
    <item>
      <title>Inter-laboratory study on formaldehyde determination by HPLC</title>
      <link>http://hdl.handle.net/2117/13670</link>
      <description>Title: Inter-laboratory study on formaldehyde determination by HPLC
Authors: Marsal Monge, Agustín; Font Vallès, Joaquim; Viera, Susanna; Cuadros, Sara; Rius Carrasco, Antoni; Reyes Reyes, Maria; Verdú, Emilio; Jorba, Montse; Juárez, Miguel-Angel
Abstract: The colorimetric determination of formaldehyde in a water extract of a leather sample is a procedure that has been criticized because of possible interferences of other aldehydes and coloured substances that could interfere in the spectrophotometric detection. The measurement by liquid chromatography HPLC is an alternative method that was developed some years ago. This method is more sophisticated but more selective and free of the aforementioned interferences. It is not sensitive to coloured extracts. With the implementation of HPLC equipment in many laboratories, this choice has become feasible in our sector. The process is selective. Formaldehyde is separated and quantified as a derivative from other aldehydes and ketones by liquid chromatography. The free-formaldehyde and formaldehyde which is hydrolysed during extraction to yield free-formaldehyde are detected by this method. The sample is eluted with water at 40ºC. The eluate is mixed with 2,4 dinitrophenylhydrazine, whereby aldehydes and ketones react to yield the respective hydrazones. These are separated by means of a reversed-phase HPLC method, detected at 350 nm and quantified. The aim of this work is to present a collaborative inter-laboratory study coordinated by the Igualada Leather Technology School and carried out with four other laboratories that had previosly implemented the HPLC method or that were planning to do this. Determination of formaldehyde content in leather was carried out in each laboratory in accordance with prEN ISO 17226:2005 - HPLC Standard, developed by the Committee CEN/TC 289. Part 2 of the ISO 5725 Standard (Basic method for the determination of repeatability and reproducibiliry of a standard measurement method) was applied to examine the results. The study proved successful. The HPLC method achieved very reproducible results between laboratories. This work has also demonstrated that other aldehydes, glutaraldehyde included, do not interfere in the chromatographic method. The use of a PDA detector increases the confidence of the detection of formaldehyde in leather samples</description>
      <pubDate>Wed, 26 Oct 2011 14:45:06 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/13670</guid>
      <dc:date>2011-10-26T14:45:06Z</dc:date>
      <itunes:author>Marsal Monge, Agustín; Font Vallès, Joaquim; Viera, Susanna; Cuadros, Sara; Rius Carrasco, Antoni; Reyes Reyes, Maria; Verdú, Emilio; Jorba, Montse; Juárez, Miguel-Angel</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>The colorimetric determination of formaldehyde in a water extract of a leather sample is a procedure that has been criticized because of possible interferences of other aldehydes and coloured substances that could interfere in the spectrophotometric detection. The measurement by liquid chromatography HPLC is an alternative method that was developed some years ago. This method is more sophisticated but more selective and free of the aforementioned interferences. It is not sensitive to coloured extracts. With the implementation of HPLC equipment in many laboratories, this choice has become feasible in our sector. The process is selective. Formaldehyde is separated and quantified as a derivative from other aldehydes and ketones by liquid chromatography. The free-formaldehyde and formaldehyde which is hydrolysed during extraction to yield free-formaldehyde are detected by this method. The sample is eluted with water at 40ºC. The eluate is mixed with 2,4 dinitrophenylhydrazine, whereby aldehydes and ketones react to yield the respective hydrazones. These are separated by means of a reversed-phase HPLC method, detected at 350 nm and quantified. The aim of this work is to present a collaborative inter-laboratory study coordinated by the Igualada Leather Technology School and carried out with four other laboratories that had previosly implemented the HPLC method or that were planning to do this. Determination of formaldehyde content in leather was carried out in each laboratory in accordance with prEN ISO 17226:2005 - HPLC Standard, developed by the Committee CEN/TC 289. Part 2 of the ISO 5725 Standard (Basic method for the determination of repeatability and reproducibiliry of a standard measurement method) was applied to examine the results. The study proved successful. The HPLC method achieved very reproducible results between laboratories. This work has also demonstrated that other aldehydes, glutaraldehyde included, do not interfere in the chromatographic method. The use of a PDA detector increases the confidence of the detection of formaldehyde in leather samples</itunes:summary>
    </item>
    <item>
      <title>Auxiliary agents with non-swelling capacity used in pickling/tanning processes. Part 3.</title>
      <link>http://hdl.handle.net/2117/13641</link>
      <description>Title: Auxiliary agents with non-swelling capacity used in pickling/tanning processes. Part 3.
Authors: Marsal Monge, Agustín; Ramón, Palop; Font Vallès, Joaquim; Cot Cosp, Jaume; Frías, Vicente; Manich Bou, Albert M.
Abstract: In the present work, the behaviour of the four commercial products with non-swelling capacity in the pickling/tanning processes of sheepskins is studied. The successful application of these products to thinner skins would allow us to reduce salinity and, hence, the conductivity of waste waters.&#xD;
The results obtained by using these products are compared with those achieved by applying a conventional pickling/tanning process.</description>
      <pubDate>Mon, 24 Oct 2011 09:37:15 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/13641</guid>
      <dc:date>2011-10-24T09:37:15Z</dc:date>
      <itunes:author>Marsal Monge, Agustín; Ramón, Palop; Font Vallès, Joaquim; Cot Cosp, Jaume; Frías, Vicente; Manich Bou, Albert M.</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>In the present work, the behaviour of the four commercial products with non-swelling capacity in the pickling/tanning processes of sheepskins is studied. The successful application of these products to thinner skins would allow us to reduce salinity and, hence, the conductivity of waste waters.&#xD;
The results obtained by using these products are compared with those achieved by applying a conventional pickling/tanning process.</itunes:summary>
    </item>
    <item>
      <title>Environmental optimization of chromium recovery from tannery sludge using a life cycle assessment approach</title>
      <link>http://hdl.handle.net/2117/13605</link>
      <description>Title: Environmental optimization of chromium recovery from tannery sludge using a life cycle assessment approach
Authors: Kiliç, Eylem; Puig Vidal, Rita; Baquero Armans, Grau; Font Vallès, Joaquim; Colak, Selime; Gürler, Deniz
Abstract: Life cycle assessment (LCA) was used to evaluate the environmental impact of an oxidative chromium recovery method from tannery sludge, in comparison with the usual landfilling process. Three improvement&#xD;
options (water reduction, byproduct use and anaerobic sludge digestion) were considered. The results showed that the proposed chromium recovery process would be better environmentally than conventional landfilling in all the evaluated impact categories if the amount of chromium recovered was 43 kg per ton of sludge. This amount could be recovered if the chromium concentration was about 20 times higher than that considered in this study. Alternatively, a lower chromium concentration would produce a better result if the recovery method was optimized and implemented at industrial rather&#xD;
than laboratory scale, and if more accurate data were provided on environmental credits for avoiding the chromium production process. Thus, the recovery method is environmentally beneficial when tannery&#xD;
sludge contains a chromium concentration of about 100,000 ppm. According to the literature, such concentrations are not unusual. The results could serve as the basis for further environmental improvements&#xD;
in chromium recovery and tannery sludge management and should be used in decision-making processes, especially for end-of-pipe treatments.</description>
      <pubDate>Thu, 20 Oct 2011 15:56:58 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/13605</guid>
      <dc:date>2011-10-20T15:56:58Z</dc:date>
      <itunes:author>Kiliç, Eylem; Puig Vidal, Rita; Baquero Armans, Grau; Font Vallès, Joaquim; Colak, Selime; Gürler, Deniz</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>Life cycle assessment (LCA) was used to evaluate the environmental impact of an oxidative chromium recovery method from tannery sludge, in comparison with the usual landfilling process. Three improvement&#xD;
options (water reduction, byproduct use and anaerobic sludge digestion) were considered. The results showed that the proposed chromium recovery process would be better environmentally than conventional landfilling in all the evaluated impact categories if the amount of chromium recovered was 43 kg per ton of sludge. This amount could be recovered if the chromium concentration was about 20 times higher than that considered in this study. Alternatively, a lower chromium concentration would produce a better result if the recovery method was optimized and implemented at industrial rather&#xD;
than laboratory scale, and if more accurate data were provided on environmental credits for avoiding the chromium production process. Thus, the recovery method is environmentally beneficial when tannery&#xD;
sludge contains a chromium concentration of about 100,000 ppm. According to the literature, such concentrations are not unusual. The results could serve as the basis for further environmental improvements&#xD;
in chromium recovery and tannery sludge management and should be used in decision-making processes, especially for end-of-pipe treatments.</itunes:summary>
    </item>
    <item>
      <title>Quality handbook for the production of chromium(VI)-free leather</title>
      <link>http://hdl.handle.net/2117/12944</link>
      <description>Title: Quality handbook for the production of chromium(VI)-free leather
Authors: Font Vallès, Joaquim; Rius Carrasco, Antoni; Marsal Monge, Agustín</description>
      <pubDate>Wed, 13 Jul 2011 07:30:16 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/12944</guid>
      <dc:date>2011-07-13T07:30:16Z</dc:date>
      <itunes:author>Font Vallès, Joaquim; Rius Carrasco, Antoni; Marsal Monge, Agustín</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
    </item>
    <item>
      <title>Prevention of chromium(VI) formation by improving the tannery processes</title>
      <link>http://hdl.handle.net/2117/12916</link>
      <description>Title: Prevention of chromium(VI) formation by improving the tannery processes
Authors: Font Vallès, Joaquim; Rius Carrasco, Antoni; Marsal Monge, Agustín; Hauber, Christiane; Tommaselli, Michelle
Abstract: This work has been funded by the European Commission through the Chrom6less&#xD;
Project (CRAFT -1999-71638).&#xD;
The objectives of the project were:&#xD;
- Establishment of the analytical methodology which provided reproducible&#xD;
results that may be free of interferences.&#xD;
- Identification of the factors that facilitated or impeded the transformation of&#xD;
Cr(III) to Cr(VI).&#xD;
- Establishment of the best conditions that allowed the production of&#xD;
chromium(VI) free leather, even during the life of the product, in contact with&#xD;
environmental agents such as light or heat.&#xD;
The following partners participated in the project: Inpelsa, Dercosa, Proquip, Igualada&#xD;
Leather Technology School, CID-CSIC and Miguel Hernandez University, from Spain,&#xD;
Gmelich, Knoll Sitzleder, and Lederinstitut Gerberschule Reutlingen from Germany,&#xD;
and Conceria Il Cigno, Calzaturificio Accademia and Stazione Experimentale from&#xD;
Italy.&#xD;
Hundreds of samples have been analysed during the project. In order to study the&#xD;
influence of several factors in chromium (VI) formation, a lot of skins/hides have been produced. Several leather articles (hides for clothing, footwear, upholstery, leather goods and furniture upholstery and skins for suede and double face)) have been&#xD;
manufactured free from Cr (VI).&#xD;
The main results obtained were:&#xD;
- The new analytical method CEN/TS 14495 has been validated.&#xD;
- Protective measures for the prevention of chromium (VI) formation have been&#xD;
identified.&#xD;
- New formulations for several hides/skins have been developed.&#xD;
- A handbook for the production of chromium (VI)-free leather has been&#xD;
published.&#xD;
The main conclusions of the project were:&#xD;
- The Chrom6less Project has shown that most of the skins/leathers did not&#xD;
contain hexavalent chromium.&#xD;
- It is now possible to confidently determine the Cr(VI) content in all kinds of&#xD;
leather regardless of their colour.&#xD;
- The application of protective measures developed in the Project allows leather to&#xD;
resist the effect of ageing without the formation of Cr(VI).</description>
      <pubDate>Mon, 11 Jul 2011 10:56:17 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/12916</guid>
      <dc:date>2011-07-11T10:56:17Z</dc:date>
      <itunes:author>Font Vallès, Joaquim; Rius Carrasco, Antoni; Marsal Monge, Agustín; Hauber, Christiane; Tommaselli, Michelle</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
      <itunes:summary>This work has been funded by the European Commission through the Chrom6less&#xD;
Project (CRAFT -1999-71638).&#xD;
The objectives of the project were:&#xD;
- Establishment of the analytical methodology which provided reproducible&#xD;
results that may be free of interferences.&#xD;
- Identification of the factors that facilitated or impeded the transformation of&#xD;
Cr(III) to Cr(VI).&#xD;
- Establishment of the best conditions that allowed the production of&#xD;
chromium(VI) free leather, even during the life of the product, in contact with&#xD;
environmental agents such as light or heat.&#xD;
The following partners participated in the project: Inpelsa, Dercosa, Proquip, Igualada&#xD;
Leather Technology School, CID-CSIC and Miguel Hernandez University, from Spain,&#xD;
Gmelich, Knoll Sitzleder, and Lederinstitut Gerberschule Reutlingen from Germany,&#xD;
and Conceria Il Cigno, Calzaturificio Accademia and Stazione Experimentale from&#xD;
Italy.&#xD;
Hundreds of samples have been analysed during the project. In order to study the&#xD;
influence of several factors in chromium (VI) formation, a lot of skins/hides have been produced. Several leather articles (hides for clothing, footwear, upholstery, leather goods and furniture upholstery and skins for suede and double face)) have been&#xD;
manufactured free from Cr (VI).&#xD;
The main results obtained were:&#xD;
- The new analytical method CEN/TS 14495 has been validated.&#xD;
- Protective measures for the prevention of chromium (VI) formation have been&#xD;
identified.&#xD;
- New formulations for several hides/skins have been developed.&#xD;
- A handbook for the production of chromium (VI)-free leather has been&#xD;
published.&#xD;
The main conclusions of the project were:&#xD;
- The Chrom6less Project has shown that most of the skins/leathers did not&#xD;
contain hexavalent chromium.&#xD;
- It is now possible to confidently determine the Cr(VI) content in all kinds of&#xD;
leather regardless of their colour.&#xD;
- The application of protective measures developed in the Project allows leather to&#xD;
resist the effect of ageing without the formation of Cr(VI).</itunes:summary>
    </item>
    <item>
      <title>Libro de calidad para la producción de piel y cuero libre de Cromo(VI)</title>
      <link>http://hdl.handle.net/2117/12913</link>
      <description>Title: Libro de calidad para la producción de piel y cuero libre de Cromo(VI)
Authors: Font Vallès, Joaquim; Marsal Monge, Agustín; Aparicio, Enrique; Sánchez, Daniel; Ribera, Antoni</description>
      <pubDate>Mon, 11 Jul 2011 10:29:35 GMT</pubDate>
      <guid isPermaLink="false">http://hdl.handle.net/2117/12913</guid>
      <dc:date>2011-07-11T10:29:35Z</dc:date>
      <itunes:author>Font Vallès, Joaquim; Marsal Monge, Agustín; Aparicio, Enrique; Sánchez, Daniel; Ribera, Antoni</itunes:author>
      <itunes:explicit>no</itunes:explicit>
      <itunes:keywords />
    </item>
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