35 research outputs found

    A comparative study of Si-BaSO4 and Si-CaSO4 pyrotechnic time-delay compositions

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    Slow burning Si-BaSO4 pyrotechnic delay compositions are employed commercially for intermediate to long time delays. However, there is very little information on this composition available in open literature. The reactivity of this composition was therefore characterized and compared to that of Si-CaSO4. The Si-BaSO4 composition supported combustion in the range of 20 to 60 wt.% Si in the bomb calorimeter. However, burning was only sustained between 20 and 40 wt.% Si in rigid aluminum tubes, with burning rates of between 8.4 and 16 mm s1. These values are comparable to those for the Si-CaSO4 system (6.9 – 12.5 mm s1). However, the CaSO4 based formulations tended to have higher energy output and produced more transient pressure compared to the barium sulfate compositions. Both formulations were insensitive to impact, friction and electrostatic discharge stimuli. The reaction products were a complex mixture that contained crystalline phases in addition to an amorphous phase. Although barium sulfate is insoluble in water and decidedly non-toxic, the reaction products produced by the Si-BaSO4 compositions were found to release soluble barium ions when contacted with water. This ranged from 50 to 140 mg per gram of barium sulfate reacted.AEL Mining Service. National Research Foundation of South Africa (Grant 83874).http://www.tandfonline.com/loi/uegm202017-07-31hb2016Chemical Engineerin

    Dengue fever in Dar es Salaam, Tanzania: clinical features and outcome in populations of black and non-black racial category

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    Although the incidence of dengue across Africa is high, severe dengue is reported infrequently. We describe the clinical features and the outcome of dengue according to raceduring an outbreak in Dar es Salaam, Tanzania that occurred in both native and expatriate populations. Adults with confirmed dengue (NS1 and/or IgM on rapid diagnostic test and/or PCR positive) were included between December 2013 and July 2014 in outpatient clinics. Seven-day outcome was assessed by a visit or a call. Association between black race and clinical presentation, including warning signs, was assessed by logistic regression adjusted for age, malaria coinfection, secondary dengue and duration of symptoms at inclusion. The independent association between demographic and comorbidities characteristics of the patients and severe dengue was evaluated by multivariate logistic regression that included potential confounders. After exclusion of 3 patients of mixed race, 431 patients with dengue (serotype 2, genotype Cosmopolitan) were included: 241 of black and 190 of non-black race. Black patients were younger (median age 30 versus 41 years; p < 0.001) and attended care after a slightly longer duration of symptoms (median of 2.9 versus 2.7 days; p = 0.01). Malaria coinfection was not significantly different between black (5%) and non-black (1.6%) patients (p = 0.06). The same proportion of patients in both group had secondary dengue (13 and 14%; p = 0.78). Among warning signs, only mucosal bleed was associated with race, black race being protective (adjusted OR 0.44; 95% CI 0.21-0.92). Overall, 20 patients (4.7%) presented with severe dengue. Non-black race (adjusted OR 3.9; 95% CI 1.3-12) and previously known diabetes (adjusted OR 43; 95% CI 5.2-361) were independently associated with severe dengue. Although all patients were infected with the same dengue virus genotype, black race was independently protective against a severe course of dengue, suggesting the presence of protective genetic or environmental host factors among people of African ancestry. The milder clinical presentation of dengue in black patients might partly explain why dengue outbreaks are under-reported in Africa and often mistaken for malaria. These results highlight the need to introduce point-of-care tests, beside the one for malaria, to detect outbreaks and orientate diagnosis. Clinicaltrials.gov Identifier: NCT01947075, retrospectively registered on the 13 of September 2014

    Distribution and risk factors for Plasmodium and helminth co-infections: a cross-sectional survey among children in Bagamoyo district, coastal region of Tanzania

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    Plasmodium and soil transmitted helminth infections (STH) are a major public health problem, particularly among children. There are conflicting findings on potential association between these two parasites. This study investigated the Plasmodium and helminth co-infections among children aged 2 months to 9 years living in Bagamoyo district, coastal region of Tanzania.; A community-based cross-sectional survey was conducted among 1033 children. Stool, urine and blood samples were examined using a broad set of quality controlled diagnostic methods for common STH (Ascaris lumbricoides, hookworm, Strongyloides stercoralis, Enterobius vermicularis, Trichuris trichura), schistosoma species and Wuchereria bancrofti. Blood slides and malaria rapid diagnostic tests (mRDTs) were utilized for Plasmodium diagnosis.; Out of 992 children analyzed, the prevalence of Plasmodium infection was 13% (130/992), helminth 28.5% (283/992); 5% (50/992) had co-infection with Plasmodium and helminth. The prevalence rate of Plasmodium, specific STH and co-infections increased significantly with age (p > 0.001), with older children mostly affected except for S. stercoralis monoinfection and co-infections. Spatial variations of co-infection prevalence were observed between and within villages. There was a trend for STH infections to be associated with Plasmodium infection [OR adjusted for age group 1.4, 95% CI (1.0-2.1)], which was more marked for S. stercoralis (OR = 2.2, 95% CI (1.1-4.3). Age and not schooling were risk factors for Plasmodium and STH co-infection.; The findings suggest that STH and Plasmodium infections tend to occur in the same children, with increasing prevalence of co-infection with age. This calls for an integrated approach such as using mass chemotherapy with dual effect (e.g., ivermectin) coupled with improved housing, sanitation and hygiene for the control of both parasitic infections

    Photo-fenton oxidation of methyl orange dye using South African ilmenite sands as a catalyst

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    In this study, the viability of South African ilmenite sands as a catalyst in the photo-Fentonlike degradation of methyl orange (MO) dye was investigated. The mineralogy and other properties of the material were characterized. Complete decolorization occurred under acidic conditions (pH < 4) in the presence of ilmenite and H2O2. Light irradiation accelerated the rate of reaction. Parameter optimization revealed that a pH of 2.5, UVB irradiation, 2 g/L catalyst loading, and a hydrogen peroxide concentration of 1.0 mM were required. Under these conditions, complete decolorization was observed after 45 min. Degradation kinetics were best described by the pseudofirst order (PFO) model. Rate constants of 0.095 and 0.034 min1 were obtained for 5 and 20 mg/L MO concentrations, respectively. A 37% total organic carbon removal was observed after 60 min. This suggests a stepwise MO degradation pathway with intermediate formation rather than complete mineralization. Although iron leaching was detected, the mineralogy of the catalyst recovered after the reaction was similar to the fresh catalyst.Figure S1: SEM-EDS Micrographs of three different sites (a, b and c) of the catalyst sample using EDS to determine the elemental composition.The National Research Foundation (NRF) of South Africahttps://www.mdpi.com/journal/catalystsam2022Chemical Engineerin

    Dengue fever in Dar es Salaam, Tanzania: clinical features and outcome in populations of black and non-black racial category

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    Background: Although the incidence of dengue across Africa is high, severe dengue is reported infrequently. We describe the clinical features and the outcome of dengue according to raceduring an outbreak in Dar es Salaam, Tanzania that occurred in both native and expatriate populations. Methods: Adults with confirmed dengue (NS1 and/or IgM on rapid diagnostic test and/or PCR positive) were included between December 2013 and July 2014 in outpatient clinics. Seven-day outcome was assessed by a visit or a call. Association between black race and clinical presentation, including warning signs, was assessed by logistic regression adjusted for age, malaria coinfection, secondary dengue and duration of symptoms at inclusion. The independent association between demographic and comorbidities characteristics of the patients and severe dengue was evaluated by multivariate logistic regression that included potential confounders. Results: After exclusion of 3 patients of mixed race, 431 patients with dengue (serotype 2, genotype Cosmopolitan) were included: 241 of black and 190 of non-black race. Black patients were younger (median age 30 versus 41 years; p &lt; 0.001) and attended care after a slightly longer duration of symptoms (median of 2.9 versus 2.7 days; p = 0.01). Malaria coinfection was not significantly different between black (5%) and non-black (1.6%) patients (p = 0.06). The same proportion of patients in both group had secondary dengue (13 and 14%; p = 0.78). Among warning signs, only mucosal bleed was associated with race, black race being protective (adjusted OR 0.44; 95% CI 0.21-0.92). Overall, 20 patients (4.7%) presented with severe dengue. Non-black race (adjusted OR 3.9; 95% CI 1.3-12) and previously known diabetes (adjusted OR 43; 95% CI 5.2-361) were independently associated with severe dengue. Conclusions: Although all patients were infected with the same dengue virus genotype, black race was independently protective against a severe course of dengue, suggesting the presence of protective genetic or environmental host factors among people of African ancestry. The milder clinical presentation of dengue in black patients might partly explain why dengue outbreaks are under-reported in Africa and often mistaken for malaria. These results highlight the need to introduce point-of-care tests, beside the one for malaria, to detect outbreaks and orientate diagnosis. Trial registration: Clinicaltrials.gov Identifier: NCT01947075 , retrospectively registered on the 13 of September 2014.</p

    Schematic representation of the e-POCT algorithm.

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    <p>Example of input and output screens, sensor input, and background algorithm calculations. An example of a consultation with respective input and output screens is shown on the left; the background calculations of the algorithm are displayed on the right in black; input of information from POCTs is displayed in orange. CRP, C-reactive protein; F/u, follow-up; HIV, human immunodeficiency virus; PCT, procalcitonin; POCT, point-of-care test; mRDT, malaria rapid diagnostic test; RR, respiratory rate; SaO2, oxygen saturation.</p
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