In this work,sodium dicyanamide(SD)was used as a leaching reagent for gold recovery,and the effects of the SD dosage and solution pH on the gold-leaching performance were investigated.A gold recovery of 34.8%was obtai...In this work,sodium dicyanamide(SD)was used as a leaching reagent for gold recovery,and the effects of the SD dosage and solution pH on the gold-leaching performance were investigated.A gold recovery of 34.8%was obtained when SD was used as the sole leaching reagent at a dosage of 15 kg/t.In the presence of a certain amount of potassium ferrocyanide(PF)in the SD solution,the gold recovery was found to increase from 34.8%to 57.08%.Using the quartz crystal microbalance with dissipation(QCM-D)technique,the leaching kinetics of SD with and without PF were studied.The QCM-D results indicate that the gold-leaching rate increased from 4.03 to 39.99 ng·cm^(–2)·min^(–1) when the SD concentration was increased from 0 to 0.17 mol/L,and increased from 39.99 to 272.62 ng·cm^(–2)·min^(–1) when 0.1 mol/L of PF was used in combination with SD.The pregnant solution in the leaching tests was characterized by X-ray photoelectron spectroscopy and electrospray mass spectrometry,which indicated that Au and(N(CN)2)–in the SD solution formed a series of metal complex ions,[AuNax(N(CN)2)x+2]–(x=1,2,3,or 4).展开更多
AIM: To characterise differences between three widely used colorectal cancer cell lines using ultrastructural selective staining for glycogen to determine variation in metastatic properties. METHODS: Transmission elec...AIM: To characterise differences between three widely used colorectal cancer cell lines using ultrastructural selective staining for glycogen to determine variation in metastatic properties. METHODS: Transmission electron microscopy was used in this investigation to help identify intracellular structures and morphological features which are precursors of tumor invasion. In addition to morphological markers, we used selective staining of glycogen as a marker for neoplastic cellular proliferation and determined whether levels of glycogen change between the three different cell lines. RESULTS: Ultrastructural analysis revealed morphological differences between the cell lines, as well as differentiation into two sub-populations within each cell line. Caco-2 cells contained large glycogen deposits as well as showing the most obvious morphological changes between the two sub-populations. SW480 cells also contained large glycogen stores as well as deep cellular protrusions when grown on porous filter membranes. HT-29 cells had trace amounts of glycogen stores with few cellular projections into the filter pores and no tight junction formation.CONCLUSION: Morphology indicative of metastatic properties coincided with larger glycogen deposits, providing strong evidence for the use of selective staining to determine the neoplastic properties of cells.展开更多
基金the National Naturel Science Foundation of China(Nos.51974016 and 51204012)for financial support.
文摘In this work,sodium dicyanamide(SD)was used as a leaching reagent for gold recovery,and the effects of the SD dosage and solution pH on the gold-leaching performance were investigated.A gold recovery of 34.8%was obtained when SD was used as the sole leaching reagent at a dosage of 15 kg/t.In the presence of a certain amount of potassium ferrocyanide(PF)in the SD solution,the gold recovery was found to increase from 34.8%to 57.08%.Using the quartz crystal microbalance with dissipation(QCM-D)technique,the leaching kinetics of SD with and without PF were studied.The QCM-D results indicate that the gold-leaching rate increased from 4.03 to 39.99 ng·cm^(–2)·min^(–1) when the SD concentration was increased from 0 to 0.17 mol/L,and increased from 39.99 to 272.62 ng·cm^(–2)·min^(–1) when 0.1 mol/L of PF was used in combination with SD.The pregnant solution in the leaching tests was characterized by X-ray photoelectron spectroscopy and electrospray mass spectrometry,which indicated that Au and(N(CN)2)–in the SD solution formed a series of metal complex ions,[AuNax(N(CN)2)x+2]–(x=1,2,3,or 4).
基金Supported by The Australian Research Council for fundingsome of the research reported herein through Linkage Infrastructure, Equipment and Facilities grants, No. LE0775598the ARC/NHMRC FABLS Research Network, No. RN0460002
文摘AIM: To characterise differences between three widely used colorectal cancer cell lines using ultrastructural selective staining for glycogen to determine variation in metastatic properties. METHODS: Transmission electron microscopy was used in this investigation to help identify intracellular structures and morphological features which are precursors of tumor invasion. In addition to morphological markers, we used selective staining of glycogen as a marker for neoplastic cellular proliferation and determined whether levels of glycogen change between the three different cell lines. RESULTS: Ultrastructural analysis revealed morphological differences between the cell lines, as well as differentiation into two sub-populations within each cell line. Caco-2 cells contained large glycogen deposits as well as showing the most obvious morphological changes between the two sub-populations. SW480 cells also contained large glycogen stores as well as deep cellular protrusions when grown on porous filter membranes. HT-29 cells had trace amounts of glycogen stores with few cellular projections into the filter pores and no tight junction formation.CONCLUSION: Morphology indicative of metastatic properties coincided with larger glycogen deposits, providing strong evidence for the use of selective staining to determine the neoplastic properties of cells.
