OPTIMIZATION AND KINETICS STUDIES OF THE DISSOLUTION OF DOLOMITE IN SULPHURIC ACID (H2SO4) VIA BOX-BEHNKEN EXPERIMENTAL DESIGN
Background: The recovery of any valuable component from dolomite as a double carbonate mineral depends on its dissolution efficiency. Aim: This study aimed to optimize and provide a simplified novel approach to the kinetics of dolomite dissolution in sulphuric acid solution using the Box-Behnken experimental design. Methods: The dolomite sample was dissolved in a sulphuric acid solution at seventeen different experimental conditions. The residue containing impurities was removed via filtration, while precipitation was carried out at the optimum conditions. Results and Discussion: The relationship between the independent and dependent variables best fits into the two-factor interaction model with a coefficient of determination of 0.9492, adjusted R² of 0.9187, and predicted R² of 0.7514. The total residual sum of 3x10-13 and adequate precision of 18.769 show that the predicted dissolution efficiency is much closer to the experimental values. The analysis of variance revealed that the individual effect of acid concentration, temperature, and dissolution time all positively contribute to the dissolution. The interactive effect of acid concentration with temperature and the interactive effect of temperature with dissolution time also positively influences the dissolution efficiency. Following the dissolution of dolomite in sulphuric acid, a white precipitate was formed at room temperature, which dissolved back at a temperature of 70 oC, agitation speed of 900 revolutions per minute, and within 10 minutes. A predictive approach using a two-factor interactive model was applied to generate the kinetic data. Conclusions: The established model equation is suitable for predicting dolomite dissolution in sulphuric acid. The application of the shrinking core model to the generated data shows that the reaction between dolomite and sulphuric acid is film diffusion control with a first-order reaction (0.6587) and activation energy of 27.5 KJmol-1k-1.
Read ArticleE-SELECTIN AS A BIOMARKER IN FEMALE PATIENTS WITH Β-THALASSEMIA IN AL- NAJAF PROVENCE, IRAQ
E-selectin, as identified (CD62E), is expressed on endothelial cells after stimulation with inflammation cytokines. β-Thalassemia diseases (βT) and early diagnosis are of utmost significance in the entire world population. This study was performed in the Thalassemia Center of the Al-Zahraa Educational Hospital in Al-Najaf Province, Iraq, on sixty-nine with β-thalassemia (54 βT major and 15 βT Intermedia) aged 8-40 years who transfused blood. Compared to 20 healthy volunteers as a control group. In both βT patients and healthy groups were assessed serum E-selectin levels. It was investigated the relationship with RBC, Hb, PCV, WBC, PLT, BMI, splenic status, iron, and ferritin levels. The results revealed a significant (P<0.05) decreased values of HB, RBC, P.C.V, and BMI. In contrast, values of WBC, PLT, Iron, and Ferritin were significantly increased in βT patients as compared to the healthy control groups. A significant (P<0.05) increase in serum E- Selectin level in βT patients (20.55±0.47) ng/ml to compare with the healthy group (9.16±0.50) ng/ml. Furthermore, it was a significant decrease in groups of βT major (19.87±0.42) ng/ml more than in βT intermedia (23±1.42) ng/ml. E-Selectin revealed a significant increase (P<0.05) in progress age and associated with splenectomies and underweight groups compared to splenectomies and the normal weight groups, respectively. Also, E-Selectin levels significantly positively correlated with WBC, PLT value, iron, and Ferritin levels. However, it was no significant with RBC, PCV, Hb. As a conclusion from this study, E- Selectin is an important biomarker in β-thalassemia patients can be identified as the complications associated with iron overload, inflammatory process, and endothelial dysfunction in βT disease.
Read ArticleASSESSMENT OF SERUM SCLEROSTIN LEVEL AS A BIOMARKER ASSOCIATED WITH BONE DISORDERS IN Β-THALASSEMIA PATIENTS IN AL- NAJAF CITY, IRAQ
Background: β-thalassemia is a blood disorder in which the body does not make hemoglobin normally. Aim: To assess serum sclerostin in female patients with beta-thalassemia and compare with the healthy controls and to predict its complication associated with the bone pathophysiology, for designed improvement the lifestyle goodliness for these patients. Material and methods: Sixty-nine female beta-thalassemia (βT) patients (54 βT major and 15 βT Intermedia), aged 8-40 years who dependent on transfused blood, and 20 healthy controls were evaluated serum sclerostin, and was examined the relationship with hematological parameters RBC, Hb, PCV, WBC, PLT, BMI, splenic status, iron, and ferritin levels. The information of beta-thalassemia patients was collected and records by the questioner. Results: A significantly increased serum sclerostin level (mean 26.80±0.91) pg/ml was showed in βT patients compared with the healthy controls (10.03±0.68, p smaller than 0.001) pg/ml. Furthermore, a significant decrease (p smaller than 0.05) of the sclerostin level was observed in β-thalassemia major compared to intermedia β-thalassemia patients. Serum sclerostin level revealed a significant increase in progress age; it is highest in the age group (30-40) year as compared with age group (8-18) and (19-29) year respectively. Sclerostin showed no associations with the RBC, Hb, PCV, and significantly positively correlated (p smaller than 0.05) with serum iron, ferritin levels, WBC, and PLT count. Significantly higher sclerostin levels in splenectomized and underweight groups were observed compared to unsplenectomized and normal-weight groups (p smaller than 0.05) of βT patients. Conclusions: Sclerostin plays an important role in beta-thalassemia patients and can serve as a biomarker associated with the bone pathophysiology and indicator to prevent the continuation of such serious diseases caused by iron overload in these patients.
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