Use of humic substances in froth flotation processes.

Continual growing demand for metals in regular and emerging markets has led to an increasing use of chemicals and reagents in ore processing. This trend force to incur in an increasing use of commodities which inevitable leads to higher operational costs and environmental concern. The chemicals and reagents used in flotation processes especially invoke high costs of handling and disposal due to their hazardous nature, but until now, few studies have been carried out to seek possible alternatives. In order to develop a cheaper and greener processes, these hazardous materials should be replaced by more sustainable products, by-products, or wastes generated by other industries. Biosolids, cheaper and greener than chemical frothers and collectors, have been tested successfully in flotation processes. Studies of removal rates and froth flotation kinetics have been carried out independently, nevertheless a deeper understanding of the tradeoffs involved between the rates and kinetics should be obtained. This work evaluates the use of different collectors (conventional collector (CC), biosolids (and their main components), and mixtures of CC and biosolids main components) in the froth flotation of copper sulfide ores. Tests were carried out in Denver Cells, at fixed collector, frother, and pH levels, in order to estimate metallurgical and kinetic parameters. In rougher flotation tests, biosolids show to be the most efficient non-CCs, achieving Cu recoveries of 64.1%. CC achieved 76.2% Cu recoveries while none of the pure biosolids main components achieved Cu recoveries over 60%. In the kinetics studies, only the partial replacement of CC (by 50% of Humic Acids (HAs) or biosolids) allowed a similar copper recovery once compared with CC (~81% Cu to be obtained with a fast kinetic constant of ~0.88 min-1). For molybdenum, partial replacement of CC produced better recovery and kinetics constants (k of 0.83 min-1 and R∞ of 66.10% for 50% CC - 50% HAs; k of 0.90 min-1 and R∞ of 61.79% for 50% CC - 50% biosolids). Results show that different combinations of biosolids - CC or HAs - CC could achieve optimal flotation conditions. As evaluated, an optimal combinations would allow considerable reductions in energy and chemical consumption.

An exploratory study of peat and sawdust as enhancers in the (bio)degradation of n-dodecane.

Current practice for dealing with oil spills involves the use of adsorbent materials to contain the pollution prior to bioremediation of the contaminated soil and adsorbent. This work presents a study of the effects of bioavailable carbon sources in the adsorbents peat and sawdust as organic nutrients for microorganisms specialized in degrading n-dodecane in soil and sawdust contaminated with hydrocarbon mixtures. An experimental bioremediation system was developed using n-dodecane, biomass adapted to n-dodecane, inorganic nutrients and the two adsorbents (sterilized). Bioreactors containing peat enhanced cell growth the most and also evolved more CO(2). An advantage of peat is that its soluble carbon sources can sustain higher cell densities compared to sawdust, and this may prove decisive when cultivating endogenous microorganisms for the aerobic bioremediation of soils contaminated with hydrocarbons. However, at the end of the 68-day experiment slightly higher n-dodecane removal was identified in the system containing sawdust-n-dodecane (99.6%) than in that with peat-n-dodecane (98.5%), evidencing the higher hydrocarbon retention capacity of peat. Based on this study, the use of sawdust instead of peat is recommended when an adapted inoculum is available for aerobic bioremediation of organic contaminants, whereas the use of peat is advisable to boost cell densities in order to improve the probability of sustaining a viable biomass in unfavorable conditions.

Bioremediation of contaminated mixtures of desert mining soil and sawdust with fuel oil by aerated in-vessel composting in the Atacama Region (Chile).

Since early 1900s, with the beginning of mining operations and especially in the last decade, small, although repetitive spills of fuel oil had occurred frequently in the Chilean mining desert industry during reparation and maintenance of machinery, as well as casual accidents. Normally, soils and sawdust had been used as cheap readily available sorbent materials of spills of fuel oil, consisting of complex mixtures of aliphatic and aromatic hydrocarbons. Chilean legislation considers these fuel oil contaminated mixtures of soil and sawdust as hazardous wastes, and thus they must be contained. It remains unknown whether it would be feasible to clean-up Chilean desert soils with high salinity and metal content, historically polluted with different commercial fuel oil, and contained during years. Thus, this study evaluated the feasibility of aerated in-vessel composting at a laboratory scale as a bioremediation technology to clean-up contaminated desert mining soils (fuel concentration>50,000 mg kg(-1)) and sawdust (fuel concentration>225,000 mg kg(-1)) in the Atacama Region. The composting reactors were operated using five soil to sawdust ratios (S:SD, 1:0, 3:1, 1:1, 1:3, 0:1, on a dry weight basis) under mesophilic temperatures (30-40 degrees C), constant moisture content (MC, 50%) and continuous aeration (16 l min(-1)) during 56 days. Fuel oil concentration and physico-chemical changes in the composting reactors were monitored following standard procedures. The highest (59%) and the lowest (35%) contaminant removals were observed in the contaminated sawdust and contaminated soil reactors after 56 days of treatment, respectively. The S:SD ratio, time of treatment and interaction between both factors had a significant effect (p<0.050) on the contaminant removal. The results of this research indicate that bioremediation of an aged contaminated mixture of desert mining soil and sawdust with fuel oil is feasible. This study recommends a S:SD ratio 1:3 and a correct nutrient balance in order to achieve a maximum overall hydrocarbon removal of fuel oil in the weathered and aged contaminated wastes.