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Search for direct scalar top pair production in final states with two tau leptons in collisions at TeV with the ATLAS detector
Fenton-Like Oxidation of 4-Chlorophenol: Homogeneous or Heterogeneous?
Heterogeneous Fenton-like catalysts have received considerable research attention because they could potentially be attractive for oxidative removal of organic contaminants from tertiary wastewater. However, process design is still hampered by insufficient understanding of the chemical pathways involved, and especially whether oxidation activity stems from heterogeneous surface chemistry or minute concentrations of dissolved metal ions in the homogeneous phase. Using inductively coupled plasma-optical emission spectroscopy (ICP-OES) in combination with pH monitoring and ultraviolet–visible spectroscopy (UV–vis) we have monitored the degradation of 4-chlorophenol (4-CP) over two Fenton-like heterogeneous systems, namely FeOx supported on TiO2 and CuFe2O4. We show conclusively that these systems proceed predominantly through a homogeneous route via dissolved metal ions from the solid phase catalysts. Control experiments with homogeneous Fe3+ or Cu2+ systems reveal that even minute concentrations (μM/subppm) of dissolved metal ions leached from the solid phases account for the observed 4-CP degradation rates in the heterogeneous systems. ICP-OES revealed that metal leaching was time-dependent and variable because of pH variations associated with changing acid release rates. Buffering solutions at pH 7.4 suppressed metal leaching (and hence 4-CP degradation) in the FeOx/TiO2 system, but not in others. For example, pH buffering did not entirely suppress metal leaching from CuFe2O4, for which 4-CP degradation was retained through small concentrations of Fe and Cu ions in solution. Our results highlight the importance of careful monitoring of metal content in the aqueous phase, certainly with analytical sensitivity below ppm concentrations of the dissolved metals, and also the crucial influence of time-dependent pH variations on the reaction process. Recyclability of catalysts, pH buffering of solutions or monitoring of metal content in the solid phase by less sensitive analytical methods, for example, chemical analysis, gravimetry, X-ray fluorescence, or energy dispersive X-ray analysis in electron microscopes, cannot exclude the homogeneous Fenton route in the presence of solid catalysts
Prediction of AD dementia by biomarkers following the NIA-AA and IWG diagnostic criteria in MCI patients from three European memory clinics.
BACKGROUND: Proposed diagnostic criteria (international working group and National Institute on Aging and Alzheimer's Association) for Alzheimer's disease (AD) include markers of amyloidosis (abnormal cerebrospinal fluid [CSF] amyloid beta [Aβ]42) and neurodegeneration (hippocampal atrophy, temporo-parietal hypometabolism on [18F]-fluorodeoxyglucose-positron emission tomography (FDG-PET), and abnormal CSF tau). We aim to compare the accuracy of these biomarkers, individually and in combination, in predicting AD among mild cognitive impairment (MCI) patients. METHODS: In 73 MCI patients, followed to ascertain AD progression, markers were measured. Sensitivity and specificity, positive (LR+) and negative (LR-) likelihood ratios, and crude and adjusted hazard ratios were computed. RESULTS: Twenty-nine MCI patients progressed and 44 remained stable. Positivity to any marker achieved the lowest LR- (0.0), whereas the combination Aβ42 plus FDG-PET achieved the highest LR+ (6.45). In a survival analysis, positivity to any marker was associated with 100% conversion rate, whereas negativity to all markers was associated with 100% stability. CONCLUSIONS: The best criteria combined amyloidosis and neurodegeneration biomarkers, whereas the individual biomarker with the best performance was FDG-PET
Ostwald's rule and enantiotropy: polymorph appearance in the crystallisation of p-aminobenzoic acid
The development of rational crystallisation strategies in polymorphic systems requires the experimental manipulation of both kinetics and thermodynamics. We show for the first time the results of the interplay between these competing driving forces in an enantiotropic system, p-aminobenzoic acid. The outcomes are unexpected with temperature having no impact
The Dynamic Nature of Hypertrophic and Fibrotic Remodeling of the Fish Ventricle.
Chronic pressure or volume overload can cause the vertebrate heart to remodel. The hearts of fish remodel in response to seasonal temperature change. Here we focus on the passive properties of the fish heart. Building upon our previous work on thermal-remodeling of the rainbow trout ventricle, we hypothesized that chronic cooling would initiate fibrotic cardiac remodeling, with increased myocardial stiffness, similar to that seen with pathological hypertrophy in mammals. We hypothesized that, in contrast to pathological hypertrophy in mammals, the remodeling response in fish would be plastic and the opposite response would occur following chronic warming. Rainbow trout held at 10°C (control group) were chronically (>8 weeks) exposed to cooling (5°C) or warming (18°C). Chronic cold induced hypertrophy in the highly trabeculated inner layer of the fish heart, with a 41% increase in myocyte bundle cross-sectional area, and an up-regulation of hypertrophic marker genes. Cold acclimation also increased collagen deposition by 1.7-fold and caused an up-regulation of collagen promoting genes. In contrast, chronic warming reduced myocyte bundle cross-sectional area, expression of hypertrophic markers and collagen deposition. Functionally, the cold-induced fibrosis and hypertrophy were associated with increased passive stiffness of the whole ventricle and with increased micromechanical stiffness of tissue sections. The opposite occurred with chronic warming. These findings suggest chronic cooling in the trout heart invokes a hypertrophic phenotype with increased cardiac stiffness and fibrosis that are associated with pathological hypertrophy in the mammalian heart. The loss of collagen and increased compliance following warming is particularly interesting as it suggests fibrosis may oscillate seasonally in the fish heart, revealing a more dynamic nature than the fibrosis associated with dysfunction in mammals
Toward a spatial theory of taste formation
This paper argues for the development of a spatial theory of taste formation. In consumer research, taste has provided a valuable tool and it has mostly been utilized as the theoretical apparatus of our aesthetic choices, preferences, lifestyles and identity projects. However, there is no consensus on how taste is formed and performed in the contemporary marketplace. Consumer researchers have engaged more with the functions and consequences rather than with spatial processes of taste formation. Existing theories of taste are limited due to their primary focus either on consumption practices and/or on postmodern assertions about the fluidity and fragmentation of consumers’ tastes. Based on a review of previous literature on aesthetics, theories of taste and aesthetic consumption experiences, we illustrate how taste might be understood as being spatially formed and performed through consumers’ aesthetic experiences at various consumption places. We highlight the importance of consumers’ aesthetic experiences and their spatial context to the formation of tastes. Inspired by a phenomenological interpretation of Bourdieuian theories of taste and their subsequent use within consumer research, we argue for the development of a spatial theory of taste formation. This reveals the importance of consumption places, which are culturally embedded within certain fields of consumption, and the diversity of ways that consumers’ aesthetic experiences and identity investments within these places might be related to their tastes and identity projects. Accordingly, we argue that a spatial theory of taste offers consumer researchers the possibility to investigate the topoanalytic relationality of consumers’ tastes and also place their identity projects within a physical, socio-cultural, and historical frame. We conclude by illustrating how a spatial theory of taste formation might be of relevance to diverse streams of consumer research. We also explain why such a theoretical shift toward a spatial conception of taste would be useful for contemporary marketing theory and practice
Pioglitazone and bladder cancer risk: a multipopulation pooled, cumulative exposure analysis.
AIMS/HYPOTHESIS: The evidence on the association between pioglitazone use and bladder cancer is contradictory, with many studies subject to allocation bias. The aim of our study was to examine the effect of exposure to pioglitazone on bladder cancer risk internationally across several cohorts. The potential for allocation bias was minimised by focusing on the cumulative effect of pioglitazone as the primary endpoint using a time-dependent approach. METHODS: Prescription, cancer and mortality data from people with type 2 diabetes were obtained from six populations across the world (British Columbia, Finland, Manchester, Rotterdam, Scotland and the UK Clinical Practice Research Datalink). A discrete time failure analysis using Poisson regression was applied separately to data from each centre to model the effect of cumulative drug exposure on bladder cancer incidence, with time-dependent adjustment for ever use of pioglitazone. These were then pooled using fixed and random effects meta-regression. RESULTS: Data were collated on 1.01 million persons over 5.9 million person-years. There were 3,248 cases of incident bladder cancer, with 117 exposed cases and a median follow-up duration of 4.0 to 7.4 years. Overall, there was no evidence for any association between cumulative exposure to pioglitazone and bladder cancer in men (rate ratio [RR] per 100 days of cumulative exposure, 1.01; 95% CI 0.97, 1.06) or women (RR 1.04; 95% CI 0.97, 1.11) after adjustment for age, calendar year, diabetes duration, smoking and any ever use of pioglitazone. No association was observed between rosiglitazone and bladder cancer in men (RR 1.01; 95% CI 0.98, 1.03) or women (RR 1.00; 95% CI 0.94, 1.07). CONCLUSIONS/INTERPRETATION: The cumulative use of pioglitazone or rosiglitazone was not associated with the incidence of bladder cancer in this large, pooled multipopulation analysis