This study was performed to investigate the feasibility of applying a Rotary Triboelectrostatic Separator(RTS) to the beneficiation of Eshidiya phosphate minerals.RTS separation tests were carried out on phosphatic ...This study was performed to investigate the feasibility of applying a Rotary Triboelectrostatic Separator(RTS) to the beneficiation of Eshidiya phosphate minerals.RTS separation tests were carried out on phosphatic bed A_1,phosphatic bed A_3 and slime samples.The bed A_1 and slime samples were tested without desliming.Two sets of tests were performed using the A_3 sample: one was performed without desliming and the other with the A_3 sample deslimed.RTS separation tests as initially performed on the bed A_1 and slime samples gave products that had essentially the same P_2O_5 content.This indicated that adsorbed clay particles on the phosphate surface are responsible for the poor separation of un-deslimed phosphates.Better triboelectrostatic separation was observed with the undeslimed A_3 phosphate sample;these tests resulted in a highest product grade of 26%P_2O_5.The deslimed A_3 sample showed far more effective separation than the undeslimed A_3 one.In fact,a concentrate of 34%P_2O_5 was obtained from the triboelectrcstatic separation of deslimed A_3.The results indicate that with deslimed A_3 P_2O_5 recovery was about 65%for a concentrate of 28%P_2O_5 and about 45%for a concentrate of 30%P_2O_5.These results clearly show the importance of desliming for effective beneficiation of phosphate by the RTS.A more efficient separation can be expected from optimized operating conditions and circuit configuration.展开更多
The study was conducted for the detection of Listeria monocytogenes bacteria from different sources (CSF and blood) obtained from patients in Pediatric hospital and from food sources like (yogurt, raw vegetables an...The study was conducted for the detection of Listeria monocytogenes bacteria from different sources (CSF and blood) obtained from patients in Pediatric hospital and from food sources like (yogurt, raw vegetables and raw milk, sausage). Ten isolates were isolated from 150 specimens one of them from CSF and one isolate isolated from blood samples the others isolated from food specimens 6 isolates isolated from sausage and 2 from raw vegetables. Isolates were identified traditionally involved culture methods based on selective enrichment and plating followed by the characterization of Listeria spp. based on colony morphology, sugar fermentation and haemolytic properties, identification by Api listeria was done. Determine the isolates that produce biofilm by tissue culture plate method. The highest biofilm forming strains ofListeria monocytogenes isolates appear in No. (D10, El, E5 and E7) OD reading each of them is (0.13, 0.09, 0.11 and 0.19) respectively, the lowest or poor biofilm forming strains appear in No. (D11, D12, E2, E3, E4 and E6) that optical density (OD) reading are (0.04, 0.03, 0.05, 0.04, 0.05 and 0.03) respectively by comparing with control prepared in well (A12) that stained by crystal violate without putting any isolates and the OD reading is (0.003). Confirmation by PCR was done only for four isolates that produce biofilm (D10 and El) that obtained from CSF and blood sample and for (E5 and E7) that obtained from food samples.展开更多
基金the staff of the Jordan Phosphate Mines Company for supplying the sample used in the present work.
文摘This study was performed to investigate the feasibility of applying a Rotary Triboelectrostatic Separator(RTS) to the beneficiation of Eshidiya phosphate minerals.RTS separation tests were carried out on phosphatic bed A_1,phosphatic bed A_3 and slime samples.The bed A_1 and slime samples were tested without desliming.Two sets of tests were performed using the A_3 sample: one was performed without desliming and the other with the A_3 sample deslimed.RTS separation tests as initially performed on the bed A_1 and slime samples gave products that had essentially the same P_2O_5 content.This indicated that adsorbed clay particles on the phosphate surface are responsible for the poor separation of un-deslimed phosphates.Better triboelectrostatic separation was observed with the undeslimed A_3 phosphate sample;these tests resulted in a highest product grade of 26%P_2O_5.The deslimed A_3 sample showed far more effective separation than the undeslimed A_3 one.In fact,a concentrate of 34%P_2O_5 was obtained from the triboelectrcstatic separation of deslimed A_3.The results indicate that with deslimed A_3 P_2O_5 recovery was about 65%for a concentrate of 28%P_2O_5 and about 45%for a concentrate of 30%P_2O_5.These results clearly show the importance of desliming for effective beneficiation of phosphate by the RTS.A more efficient separation can be expected from optimized operating conditions and circuit configuration.
文摘The study was conducted for the detection of Listeria monocytogenes bacteria from different sources (CSF and blood) obtained from patients in Pediatric hospital and from food sources like (yogurt, raw vegetables and raw milk, sausage). Ten isolates were isolated from 150 specimens one of them from CSF and one isolate isolated from blood samples the others isolated from food specimens 6 isolates isolated from sausage and 2 from raw vegetables. Isolates were identified traditionally involved culture methods based on selective enrichment and plating followed by the characterization of Listeria spp. based on colony morphology, sugar fermentation and haemolytic properties, identification by Api listeria was done. Determine the isolates that produce biofilm by tissue culture plate method. The highest biofilm forming strains ofListeria monocytogenes isolates appear in No. (D10, El, E5 and E7) OD reading each of them is (0.13, 0.09, 0.11 and 0.19) respectively, the lowest or poor biofilm forming strains appear in No. (D11, D12, E2, E3, E4 and E6) that optical density (OD) reading are (0.04, 0.03, 0.05, 0.04, 0.05 and 0.03) respectively by comparing with control prepared in well (A12) that stained by crystal violate without putting any isolates and the OD reading is (0.003). Confirmation by PCR was done only for four isolates that produce biofilm (D10 and El) that obtained from CSF and blood sample and for (E5 and E7) that obtained from food samples.