The aim of this study was to investigate the usefulness of a membrane hybrid process for the treatment of real textile wastewater (TWW) and its potential reuse in the dyeing of cotton knitted fabric ...(DCF) process. To determine a suitable pretreatment, sand filtration, coagulation, and UF hollow fiber (UF–HF) were compared on a laboratory scale in terms of turbidity, color, and total organic carbon (TOC). Here, UF-HF provided the best removal results of 93.6%, 99.0%, and 29.0%, respectively. The second stage involves the study of UF flat sheet membranes (5, 10, 20, and 50 kDa). The 5 kDa membrane provided the best permeate quality according to the chemical oxygen demand (COD), turbidity, TOC, conductivity, and color by 54.5%, 83.9%, 94.2%, and 45.7–83.3%, respectively. The final step was treatment with nanofiltration (NF) and reverse osmosis (RO) and these effluents were reused for dyeing. Finally, the effluents from UF-HF/5 kDa UF/RO (Scenario 1) and UF-HF/5 kDa UF/NF (Scenario 2) were analyzed for turbidity, COD, TOC, biological oxygen demand, conductivity, hardness, anions and cations, and color. Both scenarios provided high removal results of 76.3–83.5%, 94.6–97.7%, 88.5–99%, 95.4–98.0%, 59.2–99.0%, 88.7–98.7%, 60.7–99.1%, and 80.0–100%, respectively. They also satisfied the DCF tests compared to the standard DCF samples. The innovative aspect of this research is as follows: 1) the complete analysis of hybrid membrane separation processes for the purpose of reuse of treated textile wastewater and 2) the proposal of a new criterion for reuse for DCF.
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•Usefulness of hybrid membrane process for reuse in textile dyeing was established.•ZW-1/5 kDa UF/NF–RO showed removal efficiencies of monitored parameters of 59–100%.•High color fastness of dyed textile with ZW-1/5 kDa UF/NF permeate was achieved.•New reuse criteria for dyeing cotton knitted fabric were proposed.•Treatment ZW-1/5 kDa UF/NF shows the better economic efficiency of 395.656,00 €.
This paper reports an experimental investigation of the thermal properties of frozen tap, demineralized, and sea water. The presented research assists in a better understanding of the thermal ...properties of ice and the processes within it and contributes regarding the generation of novel experimental data. The thermal conductivity was measured in a range from −14 °C to −33 °C using the Transient Plane Source (TPS) method. Ice blocks were placed in an expanded polystyrene box in the freezer, which is where the measurements took place. The thermal conductivity of the tap water ice was observed to vary in a range from 1.915 ± 0.005 Wm−1K−1 at −14 °C to 2.060 ± 0.004 Wm−1K−1 at −33 °C. The values obtained for the ice made of demineralized water differed by less than 10%. The thermal conductivity of the sea ice was shown to be more temperature dependent, with the values ranging from 1.262 ± 0.005 Wm−1K−1 at −14 °C to 1.970 Wm−1K−1 ± 0.004 at −33 °C. A noticeable fall in the thermal conductivity of the sea ice was observed in the temperature range from −26 °C to −19 °C. A possible reason for this could be the increased precipitation of salt in that temperature range. Measurements of thermal diffusivity displayed similar trends as those of thermal conductivity. Specific volumetric heat capacity was indirectly calculated.
Myocardial bridging (MB) is defined as a coronary artery that tunnels through the myocardium, under the overlying muscle bridge. It almost exclusively affects the left anterior descending artery ...(LAD), especially the middle part (midLAD).
Cerebrotendinous xanthomatosis (CTX) is a genetic disorder of the cholesterol metabolic pathway, most often associated with variants in the CYP27A1 gene. The dysregulation of cholesterol metabolism ...results in the accumulation of metabolites such as cholestanol, which has a predilection for neuronal tissue and tendons. The condition is treatable with chenodeoxycholic acid (CDCA), which halts the production of these metabolites. We present two adult brothers, without diagnosis, suffering from ataxia, general muscle weakness and cognitive deficits. Both brothers suffered from early onset cataracts, watery stools and thoracic kyphoscoliosis. Magnetic resonance imaging revealed hyperintense alterations in the central nervous system and intratendinous xanthomas in the Achilles tendons. A biochemical analysis showed elevated levels of cholestanol, lathosterol and 7-dehydrocholesterol. Their family history was negative for neurological and metabolic disorders. Genetic testing revealed a pathogenic
variant (c.1184+1G>A) in both brothers, confirming the diagnosis. The patients were started on CDCA therapy and have shown significant improvement at their follow-up examinations. Early diagnosis and treatment initiation in CTX patients is of great importance, as the significant reversal of disease progression can be achieved. For this reason, clinical genetic testing is necessary when it comes to patients with an onset of cataracts, chronic diarrhea, and neurological symptoms in early childhood.
ESP has become an increasingly important branch of ELT imposing new requirements and criteria to be met by teaching professionals and ESP practitioners. Designing an ESP course is one of these ...requirements, with learner needs analysis as its key first stage informing further steps within this complex cyclical process. This paper presents and discusses the results of a needs analysis of students of security studies in relation to their professional careers as perceived by first- and second-year students and the academic staff of the University of Belgrade - Faculty of Security Studies. Questionnaires were administered to these three groups of stakeholders, who were asked to evaluate the importance of language sub-activities within communicative language activities for students' professional careers. Their evaluations were analysed to identify the most important language activities for all three groups and then compared to find similarities and differences in their perceptions. This paper offers insight into how these findings can be used to inform course design so as to best reflect security students' needs and enable them operate effectively within target communicative situations.
Summary
AIM OF THE STUDY: We have done a study investigating the value of some less frequently considered Blink reflex parameters for establishing the diagnosis of idiopathic trigeminal neuralgia. ...PATIENTS: The study was done on 50 patients suffering from idiopathic trigeminal neuralgia, diagnosed according to the guidelines of the International Classification of Headache Disorders, with no other apparent illness. METHODS: We have stimulated the supraorbital nerve at the forehead (foramen n. supraorbitalis) and recorded the reflex response on both mm. orbiculares oculi. Incidence of following findings was determined: (1) occurrence of ipsilateral R3 component, (2) prolonged duration (>25 ms) of R2 when stimulating the affected side and (3) occurrence of R1 component during the stimulation of contralateral supraorbital nerve. We have compared these findings to those of 50 healthy subjects from the control group (Chi-square,
p
< 0.05). Sensitivity, specificity and diagnostic value for individual parameters were determined. RESULTS AND CONCLUSION: All three parameters tested proved to have a significantly higher incidence in the group of subjects. The occurrence of R3 component on the affected side showed the highest diagnostic value. Significance: We believe these findings could electrophysiologically reinforce the clinically established diagnosis of idiopathic trigeminal neuralgia.
Pineal cysts occur in all ages, predominantly in adults in the fourth decade of life. In series of magnetic resonance imaging (MRI) studies, the prevalence of pineal cysts ranged between 1.3% and ...4.3% of patients examined for various neurologic reasons and up to 10.8% of asymptomatic healthy volunteers. The diagnosis of pineal cyst is usually established by MRI with defined radiological criteria to distinguish benign pineal cyst from tumors of this area. A recent study demonstrated the findings obtained by transcranial sonography to correspond to those obtained by MRI in the detection of both pineal gland cyst and pineal gland itself, and could be used in the future mainly as follow up examination. Pineal cysts usually have no clinical implications and remain asymptomatic for years. The most common symptoms include headache, vertigo, visual and oculomotor disturbances, and obstructive hydrocephalus. Less frequently, patients present with ataxia, motor and sensory impairment, mental and emotional disturbances, epilepsy, circadian rhythm disturbances, hypothalamic dysfunction of precocious puberty, and recently described occurrence of secondary parkinsonism. Symptomatic cysts vary in size from 7 mm to 45 mm, whereas asymptomatic cysts are usually less than 10 mm in diameter, although a relationship between the cyst size and the onset of symptoms has been proved to be irrelevant in many cases. There is agreement that surgical intervention should be undertaken in patients presenting with hydrocephalus, progression of neurologic symptoms, or cyst enlargement. Tissue sample of the pineal lesion can be obtained by open surgery, stereotaxy and neuroendoscopy.
Cerebrotendinous xanthomatosis (CTX) is a genetic disorder of the cholesterol metabolic pathway, most often associated with variants in the CYP27A1 gene. The dysregulation of cholesterol metabolism ...results in the accumulation of metabolites such as cholestanol, which has a predilection for neuronal tissue and tendons. The condition is treatable with chenodeoxycholic acid (CDCA), which halts the production of these metabolites. We present two adult brothers, without diagnosis, suffering from ataxia, general muscle weakness and cognitive deficits. Both brothers suffered from early onset cataracts, watery stools and thoracic kyphoscoliosis. Magnetic resonance imaging revealed hyperintense alterations in the central nervous system and intratendinous xanthomas in the Achilles tendons. A biochemical analysis showed elevated levels of cholestanol, lathosterol and 7-dehydrocholesterol. Their family history was negative for neurological and metabolic disorders. Genetic testing revealed a pathogenic CYP27A1 variant (c.1184+1G>A) in both brothers, confirming the diagnosis. The patients were started on CDCA therapy and have shown significant improvement at their follow-up examinations. Early diagnosis and treatment initiation in CTX patients is of great importance, as the significant reversal of disease progression can be achieved. For this reason, clinical genetic testing is necessary when it comes to patients with an onset of cataracts, chronic diarrhea, and neurological symptoms in early childhood.
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