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化學

開發回收PET合成UiO-66並應用於催化合成羥甲香豆素

本研究利用乙二醇處理後的聚對苯二甲酸(PET)及氯氧化鋯,以創新的無溶劑方式”solvent-free PET-to-MOF conversion”合成一類金屬有機框架材料(MOF) ── UiO-66(Zr),並發現此材料可用於催化Pechmann condensation、以間苯二酚和乙醯乙酸乙脂合成羥甲香豆素。於190℃之環境下,乙二醇處理6小時的EG-PET可合成出晶型最接近模擬模型的UiO-66晶體;而我們開發的合成方法中,最佳的反應條件為反應物質量比(氯氧化鋯:PET)= 2:1、130℃合成24小時。 對於合成出的UiO-66(Zr),我將其進行了XRD、FTIR、BET、SEM檢測,結果符合UiO-66(Zr)的特徵;唯比表面積僅有約900 平方公尺/克,推測此方法合成出的材料之有機linker數量和一般UiO-66(Zr)有所差異。 對於催化合成羥甲香豆素之反應,我們首先發現UiO-66(Zr)可作為非勻相催化劑參與此反應;且實驗結果顯示,相較於溶劑熱合成的UiO-66(Zr),以本研究的方法所得之UiO-66(Zr)作為催化劑可得到更高產率的羥甲香豆素。

Synthesis of Nanocomposite Nanocellulose From Durio zibethinus L. and TiO2 NPs as Potential Food Packaging Antibacterial (E. coli Wild Type and Resistance)

According to the 印尼n Association of Olefin Aromatic and Plastic Industries/INAPLAS, 2019 national plastic consumption still relies on plastic packaging at 65% and surprisingly, around 60% of plastic waste is absorbed by the food and beverage industry. The waste has been widely sought to be environmentally friendly, one of which is by developing biodegradable packaging. The purpose of this research is to make durian peel cellulose nanocomposites impregnated with TiO2 NPs, to form antibacterial properties against E. coli wild type and resistance. In this research, there are research methods consisting of nanocomposite synthesis, PSA test, FTIR, physical characteristics test and resistance test. The results analyzed that the nanocomposite nanocellulose-TiO2 NPs was successfully made using a 1:1 ratio and had a particle size of 458.7 nm based on the PSA test, which is classified as a nano size. The success of nanocomposite synthesis was proven by the results of FTIR analysis, which showed the formation of 698.65cm-1 and 1633.99cm-1 spectra, indicating the peak of TiO2 NPs and O-H functional groups on TiO2 NPs, as well as 1028.98cm-1 and 1158.42cm-1 showing C-O and C-O-C bonds in cellulose. The antibacterial test performed showed no significant activity in disc diffusion and well diffusion tests against E. coli wild type and resistance. This is potentially caused by inhomogeneous particle size variation. Physical characteristics test showed that the tensile strength test (0.075 > 0.0125 MPa) Durio Nano-Pack is superior to styrofoam, but the compressive strength test (0.125 > 0.875 MPa) shows the opposite. In this study, nanocomposite has a potential innovation that provides good mechanical properties and has a dual function mechanically as bio-based food packaging and chemically as antibacterial. Further research is needed to improve the particle size homogeneity of nanocomposites, modify the impregnation method, so that it has the potential to develop multifunctional materials that excel in various applications.

探究螢光單體分子對激發複合體發光性質的影響及其應用

本研究設計與合成一系列的電子供體分子,以研究分子單體的化學結構對於所形成的激發複合體光物理性質的影響。 五個所設計的供體分子已被成功的合成並確定均具有分子內電子轉移的性質 其躍遷偶級距變化分布範圍在17.6-28.6D之間。 將此五個供體分子分別與兩種電子受體分子在溶液聚集在一起,利用在長波長處所新生的螢光發光,推測激發複合體的形成。研究的成果並顯示,具有類似三角形結構的供體分子將更容易形成激發複合體,而具有棒狀結構的分子則較不易形成之。此成果有效的提供有關於單體分子結構的設計對於所需激發複合體光物理性質的影響,形成可快速地提供各式不同發光波長的材料,將可作為在發光二極體發光層材料、螢光感測器、生物成像等領域需求時的分子設計藍圖與指引。

一價銠金屬催化肉桂胺衍生物進行不對稱氫芳基化反應 Rhodium(I)-Catalyzed Asymmetric Hydroarylation of Cinnamylamine Derivatives

一價銠金屬催化反應已經被廣泛應用於有機化學合成領域中。而本研究以具保護基之肉桂胺衍生物1與四芳基硼鈉試劑2a作為起始物進行銠金屬不對稱氫芳基化催化反應,得到具有保護基的掌性2,3-雙芳基丙胺衍生物3,並探討此反應的掌性雙烯配基對於反應的影響。本研究已完成使用Ts(對甲苯磺醯基)保護基之肉桂胺衍生物1a作為起始物進行反應,並改變與銠金屬錯合的配基,發現當配基使用2,5號位為芳基取代之配基L(掌性雙環[2,2,1]雙烯配基)時,反應有較好的位置選擇性,其中最佳的是芳基取代為苯基之配基L1,其位置選擇性比例為1:0:0.09。目前將進行改變起始物1之氮上的保護基,以L1作為配基進行反應,並與1a比較,優化反應性及產率。

Synthesis of functionalized mesoporous silica nanoparticles as drug delivery carriers for therapeutic agents

奈米藥物在臨床治療引入了重大創新。多孔性二氧化矽奈米粒子(mesoporous silica nanoparticle) 具有生物相容性和高孔隙度的特性,被運用在奈米藥物傳遞和標靶治療。奈米粒子經過表面修飾可提高藥物載荷效能以達到有效的治療。 本研究建立一項有效的奈米藥物傳遞載體的開發系統,目標在合成多孔性二氧化矽奈米粒子,使用幾丁聚糖對表面進行修飾,以提升地塞米松藥物載荷和穩定的藥物釋放。應用 X-射線繞射和傅立葉轉換紅外光譜來分析奈米粒子產物和表面官能基。應用分光光譜儀進行測定藥物的載荷和釋放速率。幾丁聚糖修飾包覆的多孔性二氧化矽奈米粒子具有 53.7%的藥物載荷率,比較未修飾的粒子只有 27.9%。藥物釋放實驗,幾丁聚糖包覆的二氧化矽奈米粒子可以延緩藥物釋放,在 5 天釋放 19.7%的地塞米松。本次研究說明幾丁聚糖包覆多孔性二氧化矽奈米粒子是有潛力的奈米藥物載體。

血跡檢測-色素替代試劑與現行酚酞法之比較

在刑事犯罪案件中,血液經常作為物證出現,檢測血液的存在是鑑識犯罪現場的一項基本任務,因此研發並採用許多血跡檢測方法,魯米諾測試就是其中之一。而卡斯特-梅爾呈色試驗等傳統測試通常用於快速篩選可疑污漬中是否含有血液。這些呈色測試不僅低成本,而且可以快速檢測其為陰性或陽性,使其適合在犯罪現場篩選潛在的血跡。在本研究中,我們將 KM 試劑、靛藍胭脂紅試劑和亮藍試劑透過呈色分析進行血跡檢測,另外使用 OpenCV 來協助判讀試劑顏色變化。結果顯示,KM 試劑的靈敏度優於靛藍胭脂紅試劑,其檢測極限濃度分別為 10-2%(w/w)和 10-1%(w/w)。另外這兩種試劑均對含有次氯酸鈉的漂白水產生偽陽性。

製備藻類衍生物碳點與 Mxene複合材料並應用高效超級電容

本研究運用綠藻、螺旋藻、卡拉膠(k,i,λ)進行製備碳點並應用高效超級電容。本實驗已完成綠藻、螺旋藻、卡拉膠( k,i,λ)在不同的pH值中的溶解度測試,並找出綠藻、螺旋藻、卡拉膠(k,i,λ)各自適合溶解的溫度及溶液。此外,中途也已透過文獻中的實驗證實我們實驗中所運用的電化學實驗設計及裝置可以成功製備出碳點。而在電化學製備碳點的部分目前完成單獨藻類、藻類加histidne的電擊實驗以及測其吸收光譜,也運用先前製備出較穩定的碳點加入MXene進行電化學分析,透過碳點擴大MXene分層,以達到增加MXene電化學效能的效果。最後,預計之後將進行更多的電化學分析,進一步地確認碳點結合MXene能在超級電容的應用。

Resolving the Phosphate Fertilizer Dilemma through Progressive Wastewater Treatment

The study aimed to resolve global phosphate scarcity by developing a cost-effective method for phosphorus recovery from industrial wastewater. In existing wastewater treatment, oxidizing phosphite ions (PHO32-) posed a significant challenge. However, our research aimed to develop an effective method for this oxidation process, crucial for phosphorus recovery in industrial wastewater treatment. By utilizing low-cost iron compounds and innovative catalysts, such as iodine obtained from seawater and copper, we achieved remarkable success. Our method demonstrated the ability to oxidize over 80% of PHO32- into phosphate ions (PO43-) within 120 minutes, overcoming the limitations of existing costly methods involving palladium catalysts or high-voltage conditioned ozone (O3). Moreover, the process exhibited profitability, with a gross profit of $1.84 per kilogram of phosphorus, presenting a drastic reduction in cost compared to conventional methods using palladium catalysts. This breakthrough not only offers sustainable wastewater purification but also promises a pathway for resource recovery. Additionally, our future prospects involve refining this method into a device capable of purifying industrial wastewater and recovering phosphorus, emphasizing sustainability and reduced power consumption through innovative techniques like using iron and carbon plates forming a battery. This novel technology represents a sustainable solution utilizing abundant resources such as iodine from seawater, iron, and calcium, paving the way for sustainable phosphorus resource recovery.

Observation of volcanic gases with a simple alkaline filter paper method at Sakurajima Volcano in Kagoshima, Japan.

There are many active volcanoes in Kagoshima Prefecture, including Sakurajima Volcano. So, the volcanic disaster prevention is an urgent issue. Also, Hirabayashi of Tokyo Institute of Technology reported that the molar ratio of HCl/SO2 is large during periods of high HCl/SO2 and conversely small during periods of low HCl/SO2 , and that explosions increase one month after the molar ratio of HCl/SO2 increases during periods of no explosions. We decided to determine the composition ratio of volcanic gases (sulfur dioxide, hydrogen chloride, and hydrogen fluoride) emitted from Sakurajima crater in order to understand and predict volcanic activities. Th us, we established a simple collection method for volcanic gases using alkaline filter paper and a quantitative method using a self m ade absorbance photometer so that even high school students could perform the measurement at many points, and we discussed the data from various perspectives. Furthermore, since last year, we have found a correlation between the variation of Cl-/SO2 ratio and the number of eruptions at Sakurajima volcano. Also, a model for the behavior of volcanic gases was developed based on a comparison of the amount of volcanic ash and the number of eruptions.

二氧化鋯量子點在文物修復與減碳科技應用的潛力

本研究成功以水熱法在 110°C 下合成了約3.90 nm 大小的ZrO2量子點(QDs)。此設計的ZrO2 QDs 能隙為5.03 eV(波長λ < 300 nm),在可見光和紫外光範圍內無明顯吸收特徵,呈現高度惰性和穩定性,適合應用於抗紫外線塗層或顏料。而ZrO2 QDs 表面豐富的氧空位與不同溫度下的CO₂轉化率及CO/CH₄產物選擇性相關。氧空位為帶部分正電的酸性活性位,CO2作電子受體為路易士酸。經氧氣環境加熱處理後的ZrO2 QDs 能提高CO2轉化率且在低溫條件下選擇性較高能促進電子轉移生成CH₄(每分子8e⁻ 轉移)。不同金屬簇(如Fe、Ni、Co和Cu)表面修飾後,Fe-ZrO2 QDs 被證明為最佳催化劑,低溫下更有效促進CH₄生成,且優於ZrO2 QDs。這顯示Fe與ZrO2間存在顯著的強金屬-載體相互作用(SMSI),提升Fe捕捉CO₂分子的能力。此特性突顯ZrO2於碳減排技術的潛力,能有效將CO₂轉化為可再利用的碳基燃料或化學原料,為減少溫室氣體提供實用解決方案。