Fast Fabulous Flush
Water is very vital in our lives as we cannot live without it. However our world is now facing a serious problem. Owing to the increasing population, water resources are scarce. In recent years, we can see that droughts have been affecting millions of people around the globe. In the meantime, people in developed countries have been wasting huge amount of water for flushing the toilet. According to the US Environmental Protection Agency, 30% of household water goes toward flushing the toilet. Countries like China, US, Canada and UK are still using fresh water in flushing, consuming 190 million L of fresh water every day, not to mention the energy needed in pumping the water. In fact, it is not necessary to use so much water to flush away substances like tissue, hair, urine etc. The water we used is far more than we need. However, as we cannot control how much water is used when we flush, all water in the cistern is flushed away. Realizing the seriousness of water shortage and wastage in flushing, we tried to invent a device to conserve water by controlling the amount of flushing water used. Firstly, we study the principle of normal flushing system so as to understand why flushing cannot be controlled. Then, we tried to think of ways to control flushing. We have tried various methods and materials. After the 6-month testing and modification, we successfully invented Fast Fabulous Flush. It is a device which can be fit into existing cistern to conserve water. With our invention, users can control the amount of water flushed according to needs, so as not to waste unnecessary water. Our invention costs a low price which is no more than 2 US dollar. Also, it can be fit into existing cistern within 3 minutes with simple installation process. Most importantly, flushing water can be conserved effectively. It is estimated that around 200L of water can be saved per household every day.
Anaerobic Respiration: A Novel Bioelectrochemical Copper Recovery System?
Increasing concentrations of copper in discharged effluents pose hazards to aquatic food chains. This project aimed to develop a self-sustained copper remediation system based on electrical and microbiological principles. The production of electrons during yeast fermentation was investigated to catalyze the reduction reaction of dissolved copper ions. An electrical circuit was designed to harness electrons produced from either a pure or mixed culture of yeast, and were compared for voltage outputs. This system utilized a combination of carbon cloth and copper wire as the electrodes, and a magnesium sulfate based electrolyte. The better-performing cell was subjected to copper reduction analysis, in which various initial concentrations of copper were examined. Further data analysis was carried out on the voltage outputs achieved with both the mixed and pure cultures of yeast, in which an average base line was established and voltage flunctuations were compared to that of the base line. In this way, it was possible to determine the amount and severity of each voltage flunctuation — thus demonstrating whether mixed or pure cultures of yeast produced more stable outputs. Throughout the experiment, self-constructed equipment, including arduino microcontroller moderated incubators and drip-feed systems were implemented to maintain an optimum yeast growth rate. It was found that mixed yeast cultures produced smoother electrical potential outputs in response to feeding and stress intervals. The copper recovery experiment was therefore conducted using the mixed culture. Through a series of conductivity measurements indicative of copper concentrations, metal recovery was successfully demonstrated. Trend line analysis indicated similar flunctuations between voltage output and copper recovery rates, demonstrating how copper was recovered as a result of electrons harnessed from the yeast culture. These findings can be applied to the development of an energy efficient and cost-effective copper remediation system for contaminated water effluents.
Carbon nanotubes as efficient nanosieve for controlled assembly of nanoparticles
In this work, techniques to explore the capabilities of multi-walled carbon nanotubes\r (MWNTs) in sorting nanoparticles (NPs) were presented. A droplet of a solution comprising of quantum dots (QDs) with various sizes was deposited on an aligned array of intertwined MWNTs. Photoluminescence (PL) and fluorescence microscopy (FM) revealed that MWNTs were effective nano-sieves that could effectively sort out QDs with a size difference of ~ 2.1 nm.\r Cadmium Selenide/Zinc Sulfide (CdSe/ZnS)core-shell QDs and Cadmium Sulfide (CdS) QDs were used to explore whether chemical properties of NPs affect the sieving capability of MWNTs. Further investigation on the effects of micro-patterning on the sieving ability of MWNTs was also carried out.PL and FM results suggested that micro-patterning could aid in separation of QDs and thus improve sieving capability of MWNTs. With the above findings, QDs emitting different colors as a result of size difference could efficiently be assembled onto the MWNTs en route to three-dimensional architectures with controlled assembly of NPs.\r Together with controlled laser power to remove desired amounts of QDs decorated MWNTs, a multi-colored display could be achieved. Further experiments were also carried out to determine the feasibility of introducing MWNTs as filters for NPs. Dilute solutions containing NPs such as gold colloid was run through these MWNTs filters by gravity. Field emission scanning electron microscope (FESEM) images of the samples showed that MWNTs were successful in trapping the nanoparticles. Explorations into the length dependent effect of using MWNTs as filters, suggested that 300μm MWNTs are better nano-sieves compared to 50μm MWNTs.
評估不同有機酸用於燃料電池之可行性
本研究主要著重在以三極式電化學測試探討不同有機酸燃料甲酸、草酸、檸檬酸與不同觸媒Pt/C、PtRu/C、PtPd/C 在陽極電極的氧化反應之研究。從CV 圖可得知,分子量較低的甲酸有較低的氧化電位。以CV 與LSV 圖可知,以較高的氧化電流區分,是以PtRu/C 為三種觸媒中最適合當陽極電極的;若以穩定度區分,則以PtPd/C 為最佳。我們挑選PtRu/C 此觸媒進行燃料電池放電性能測試,得到的電流不高,原因在於配置的甲酸溶液為1M,甲酸在PtRu/C 電極反應太快,質傳推動力不足,使得燃料供應不足,造成電位迅速下降。This main target of this study is using three-electrode cells to choose which Formic Acid, Oxalic Acid or Citric Acid and Pt/C, PtRu/C or PtPd/C are better for fuel cell. From CV test, Formic acid which structure is simple has the lowest oxidation potential. Combine CV with LSV, if we focus on current, PtRu/C is the best catalyst for fuel cell. But if we focus on Stability, PtPd/C has the best of them. We choose PtRu/C to do the cell performance test. The current density isn’t enough high, this is because the concentration of formic acid is just 1M. Oxidation reaction of formic acid on PtRu/C is very fast. Mass transfer driving isn’t enough for this high reaction rate, so the potential drop is very fast.