324 research outputs found
Technical note Biological treatment of industrial wastewater containing formaldehyde and formic acid
The biological treatment of wastewater from an aminoplastic resin-producing industry was studied in a pre-denitrification
system. This study reports results on the removal of organic matter and nitrogen compounds from wastewater which contained high levels of formaldehyde and formic acid. The formaldehyde concentration in the feed varied between 2 087.0 and
2 200.0 mg/ℓ, the mean removal being 99.9%. The mean efficiency of formic acid removal was 99.7%, and its concentration in the feed ranged between 1 384.6 and 1 513.9 mg/ℓ. The total organic carbon (TOC) values in the feed varied from 1 423.0 to 1 599.5 mg/ℓ, corresponding to an organic loading rate of about 0.20 kg TOC/m3·d. High TOC removal was achieved, around 92.0%. With regard to nitrogen compounds, the total Kjeldahl nitrogen (TKN) concentration in the feed ranged between 467.8 and 492.3 mg/ℓ. The applied nitrogen loading rate was around 0.06 kg TKN/m3·d, and the mean percentage of TKN removal was 76.7%. Water SA Vol 32(1)pp:115-11
A technique using a membrane flow-cell to determine average mass transfer coefficients and tortuosity factors in biofilms
Average mass transfer coefficients of an inert compound (LiCl) within denitrifying biofilms were monitored during biofilm growth in a membrane flow cell under different flow conditions, until the biofilm reached (pseudo-) steady state. Average effective diffusivities were found to increase with the decrease in tortuosity factors of the biofilm matrix. The lowest tortuosity factor corresponded to the biofilm formed under the highest liquid velocity
Complex Polysaccharide-Based Nanocomposites for Oral Insulin Delivery
Polyelectrolyte nanocomposites rarely reach a stable state and aggregation often occurs. Here, we report the synthesis of nanocomposites for the oral delivery of insulin composed of alginate, dextran sulfate, poly-(ethylene glycol) 4000, poloxamer 188, chitosan, and bovine serum albumin. The nanocomposites were obtained by Ca2+-induced gelation of alginate followed by an electrostatic-interaction process among the polyelectrolytes. Chitosan seemed to be essential for the final size of the nanocomposites and there was an optimal content that led to the synthesis of nanocomposites of 400–600 nm hydrodynamic size. The enhanced stability of the synthesized nanocomposites was assessed with LUMiSizer after synthesis. Nanocomposite stability over time and under variations of ionic strength and pH were assessed with dynamic light scattering. The rounded shapes of nanocomposites were confirmed by scanning electron microscopy. After loading with insulin, analysis by HPLC revealed complete drug release under physiologically simulated conditions
The Inviscid Limit and Boundary Layers for Navier-Stokes Flows
The validity of the vanishing viscosity limit, that is, whether solutions of
the Navier-Stokes equations modeling viscous incompressible flows converge to
solutions of the Euler equations modeling inviscid incompressible flows as
viscosity approaches zero, is one of the most fundamental issues in
mathematical fluid mechanics. The problem is classified into two categories:
the case when the physical boundary is absent, and the case when the physical
boundary is present and the effect of the boundary layer becomes significant.
The aim of this article is to review recent progress on the mathematical
analysis of this problem in each category.Comment: To appear in "Handbook of Mathematical Analysis in Mechanics of
Viscous Fluids", Y. Giga and A. Novotn\'y Ed., Springer. The final
publication is available at http://www.springerlink.co
Selective probing of magnetic order on Tb and Ir sites in stuffed Tb<sub>2+x</sub>Ir<sub>2-x</sub>O<sub>7-y</sub> using resonant X-ray scattering
We study the magnetic structure of the ``stuffed" (Tb-rich) pyrochlore iridate TbIrO, using resonant elastic x-ray scattering (REXS). In order to disentangle contributions from Tb and Ir magnetic sublattices, experiments were performed at the Ir and Tb edges, which provide selective sensitivity to Ir and Tb magnetic moments, respectively. At the Ir edge, we found the onset of long-range magnetic order below \,71\,K, consistent with the expected signal of all-in all-out (AIAO) magnetic order. Using a single-ion model to calculate REXS cross-sections, we estimate an ordered magnetic moment of at 5\,K. At the Tb edge, long-range magnetic order appeared below K, also consistent with an AIAO magnetic structure on the Tb site. Additional insight into the magnetism of the Tb sublattice is gleaned from measurements at the edge in applied magnetic fields up to 6\,T, which is found to completely suppress the Tb AIAO magnetic order. In zero applied field, the observed gradual onset of the Tb sublattice magnetisation with temperature suggests that it is induced by the magnetic order on the Ir site. The persistence of AIAO magnetic order, despite the greatly reduced ordering temperature and moment size compared to stoichiometric TbIrO, for which K and , indicates that stuffing could be a viable means of tuning the strength of electronic correlations, thereby potentially offering a new strategy to achieve topologically non-trivial band crossings in pyrochlore iridates
Coupling of magnetic order and charge transport in the candidate Dirac semimetal EuCd2As2
We use resonant elastic x-ray scattering to determine the evolution of magnetic order in EuCd2As2 below
TN = 9.5 K, as a function of temperature and applied magnetic field. We find an A-type antiferromagnetic structure
with in-plane magnetic moments, and observe dramatic magnetoresistive effects associated with field-induced
changes in the magnetic structure and domain populations. Our ab initio electronic structure calculations indicate
that the Dirac dispersion found in the nonmagnetic Dirac semimetal Cd3As2 is also present in EuCd2As2, but is
gapped for T <TN due to the breaking of C3 symmetry by the magnetic structure
Chromosome copy number changes carry prognostic information independent of KIT/PDGFRA point mutations in gastrointestinal stromal tumors
<p>Abstract</p> <p>Background</p> <p>Oncogenic point mutations in <it>KIT </it>or <it>PDGFRA </it>are recognized as the primary events responsible for the pathogenesis of most gastrointestinal stromal tumors (GIST), but additional genomic alterations are frequent and presumably required for tumor progression. The relative contribution of such alterations for the biology and clinical behavior of GIST, however, remains elusive.</p> <p>Methods</p> <p>In the present study, somatic mutations in <it>KIT </it>and <it>PDGFRA </it>were evaluated by direct sequencing analysis in a consecutive series of 80 GIST patients. For a subset of 29 tumors, comparative genomic hybridization was additionally used to screen for chromosome copy number aberrations. Genotype and genomic findings were cross-tabulated and compared with available clinical and follow-up data.</p> <p>Results</p> <p>We report an overall mutation frequency of 87.5%, with 76.25% of the tumors showing alterations in <it>KIT </it>and 11.25% in <it>PDGFRA</it>. Secondary <it>KIT </it>mutations were additionally found in two of four samples obtained after imatinib treatment. Chromosomal imbalances were detected in 25 out of 29 tumors (86%), namely losses at 14q (88% of abnormal cases), 22q (44%), 1p (44%), and 15q (36%), and gains at 1q (16%) and 12q (20%). In addition to clinico-pathological high-risk groups, patients with <it>KIT </it>mutations, genomic complexity, genomic gains and deletions at either 1p or 22q showed a significantly shorter disease-free survival. Furthermore, genomic complexity was the best predictor of disease progression in multivariate analysis.</p> <p>Conclusions</p> <p>In addition to <it>KIT/PDGFRA </it>mutational status, our findings indicate that secondary chromosomal changes contribute significantly to tumor development and progression of GIST and that genomic complexity carries independent prognostic value that complements clinico-pathological and genotype information.</p
Recent developments in genetics and medically assisted reproduction: from research to clinical applications
Two leading European professional societies, the European Society of Human Genetics and the European Society for Human Reproduction and Embryology, have worked together since 2004 to evaluate the impact of fast research advances at the interface of assisted reproduction and genetics, including their application into clinical practice. In September 2016, the expert panel met for the third time. The topics discussed highlighted important issues covering the impacts of expanded carrier screening, direct-to-consumer genetic testing, voiding of the presumed anonymity of gamete donors by advanced genetic testing, advances in the research of genetic causes underlying male and female infertility, utilisation of massively parallel sequencing in preimplantation genetic testing and non-invasive prenatal screening, mitochondrial replacement in human oocytes, and additionally, issues related to cross-generational epigenetic inheritance following IVF and germline genome editing. The resulting paper represents a consensus of both professional societies involved
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