Browsing by Author "Ruck, Kevin"
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Item A comparison of various seaweed-based diets and formulated feed on growth rate of abalone in a land-based aquaculture system(Springer, 2007) Naidoo, Krishni; Maneveldt, Gavin; Ruck, Kevin; Bolton, John J.The effects of different diets on growth in the cultured South African abalone, Haliotis midae (Linnaeus), was investigated. Growth of juvenile Haliotis midae was monitored on a commercial abalone farm over a period of 9-months in an experiment consisting of 9 treatments with 4 replicates (n = 250 individuals per replicate). The treatments were: fresh kelp (Ecklonia maxima) blades (seaweed control); Abfeed® (formulated feed control); kelp + Abfeed®; dried kelp pellets; dried kelp blades; dried kelp stipes; fresh kelp with the epiphyte Carpoblepharis flaccida; a mixed diet (Gracilaria gracilis, Ulva lactuca, and kelp) and a rotational diet (abalone were fed 1 of the 9 treatments for the first week and them kelp for the next 3 weeks). Results show that abalone grow well on all fresh seaweed combinations, but do best on a mixed diet. The likely reason for the success of the mixed diet is that the red and green seaweed was farm grown, with an increased protein content. Dried kelp in any form produced poor growth. Abalone fed on the mixed diet grew at 0.066 mm day־¹ shell length and 0.074 g day־¹ body weight; this corresponds to 24.09 mm shell length and 27.01 g body weight increase per annum. Abalone fed on dried kelp grew at only 0.029 mm day־¹ shell length and of 0.021 g day־¹ body weight. Abalone grown on Abfeed® grew at 0.049 mm day־¹ shell length and 0.046 g day־¹ body weight which corresponds to 17.88 mm and 16.79 g increase per annum; this is better than the dried seaweed feeds, but poorer than the fresh seaweed combinations. This study shows that seaweed diets, particularly if the diets include seaweeds grown in animal aquaculture effluent, are good substitutes for the formulated feeds generally used today.Item Testing the suitability of local seaweeds and formulated feed as a food source for abalone (Haliotis midae Linnaeus) in an Integrated Land-based Aquaculture System(University of the Western Cape, 2008) Naidoo, Krishnaveni; Maneveldt, Gavin W.; Ruck, Kevin; Dept. of Biodiversity and Conservation Biology; Faculty of ScienceThe direct methanol fuel cell or DMFC is emerging as a promising alternative energy source for many applications. Developed and developing countries, through research, are fast seeking a cheap and stable supply of energy for an ever-increasing number of energyconsuming portable devices. The research focus is to have DMFCs meet this need at an affordable cost is problematic. There are means and ways of making this a reality as the DMFC is found to be complementary to secondary batteries when used as a trickle charger, full charger, or in some other hybrid fuel cell combination. The core functioning component is a catalyst containing MEA, where when pure platinum is used, carbon monoxide is the thermodynamic sink and poisons by preventing further reactions at catalytic sites decreasing the life span of the catalyst if the CO is not removed. Research has shown that the bi-functional mechanism of a platinum-ruthenium catalyst is best because methanol dehydrogenates best on platinum and water dehydrogenation is best facilitated on ruthenium. It is also evident that the addition of other metals to that of PtRu/C can make the catalyst more effective and increase the life span even further. In addition to this, my research has attempted to reduce catalyst cost for DMFCs by developing a low-cost manufacturing technique for catalysts, identify potential non-noble metal catalytic systems and develop a basic process to combine various non-noblel, less expensive metallic systems to form binary, ternary and quaternary catalysts. The initial research focused on the identification of a suitable Pt/C preparation method, and characterization of the resulting catalysts by electrochemical methods (including voltammetry), elemental analysis (by EDS), and morphological characterization (by TEM). Once the preparation method for Pt/C had been established, binary (Pt–M/C), ternary (Pt–M1M2 /C) and quaternary (Pt–M1M2M3 /C) catalysts were prepared by modifying the initial Pt/C preparation method. These multi-metallic catalysts primarily function in preventing CO poisoning and allowing MeOH oxidation at the anode. To determine the effectiveness of the in-house multi-metallic catalysts the catalysts were then compared to the commercially available bench mark JM commercially available catalyst. Cyclic voltammetric and chronoamperommetric analysis revealed that the in-house catalysts electrochemical catalytic activity were similair to that of the commercially available catalysts. The Fuel application testing revealed similair trends to that of the EC activity at 0,5V (Ag/AgCl) test results, with the quaternary catalyst proving to be the most active anode catalyst producing the highest power density. The quaternary catalysts proved to be superior with its increased mass activity and high surface area (80% of the catalytic particles < 3nm).