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Curing Kinetics of Epoxy Adhesive by Non-Isothermal DSC 利用非等温 DSC 分析环氧树脂粘合剂的固化动力学
Pub Date : 2024-02-22 DOI: 10.4028/p-e5vlmg
Wiwiek Utami Dewi, Rizky Sutrisna, Heru Supriyatno, S. Astutiningsih, Mochamad Chalid
Non-isothermal DSC has been used to investigate the curing kinetics of epoxy adhesives (DGEBA-cycloaliphatic amine). The epoxy samples were scanned on DSC with five heating rates (5°C/min, 7.5°C/min, 10°C/min, 12.5°C/min, and 15°C/min). The curing kinetics were obtained through ASTM standards E2890 and E698 (the Ozawa and Kissinger methods). The kinetic parameters obtained include Ea (activation energy), A (pre-exponential factor), and n (reaction order). The activation energy calculated from the Kissinger and Ozawa method was slightly different but insignificant. The reaction rate (dα/dt) and degree of curing/conversion (α) relationship towards temperature (T), and time (t) was also investigated. The curing process's reaction rate (dα/dt) has maximum value; it can no longer increase after a specific conversion rate (α).
非等温 DSC 被用来研究环氧树脂粘合剂(DGEBA-环脂族胺)的固化动力学。环氧树脂样品以五种加热速率(5°C/分钟、7.5°C/分钟、10°C/分钟、12.5°C/分钟和 15°C/分钟)在 DSC 上扫描。固化动力学是通过 ASTM 标准 E2890 和 E698(小泽法和基辛格法)获得的。获得的动力学参数包括 Ea(活化能)、A(前指数因子)和 n(反应顺序)。基辛格法和小泽法计算出的活化能略有不同,但并不显著。此外,还研究了反应速率(dα/dt)和固化/转化程度(α)与温度(T)和时间(t)的关系。固化过程的反应速率(dα/dt)具有最大值;在特定转化率(α)之后,反应速率不再增加。
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引用次数: 0
The Performance Study of Microstrip Patch Antenna Made of Polyurethane - Oil Palm Empty Fruit Bunch Composite 聚氨酯-油棕空果束复合材料制成的微带贴片天线的性能研究
Pub Date : 2024-02-22 DOI: 10.4028/p-qch4ro
Syarifah Norsuhaila binti Syed Mahmud, Nur Iffah Zulaikha binti Azman, N. Salim, Kok Yeow You, M. Jusoh
In this paper, the performance of microstrip patch antenna that is made of fully biodegradable materials has been studied. The polymer resins of Polyurethane as a binder agent were produced using polyol extracted from palm oil while the host composites were made from oil palm empty fruit bunch fiber. The performance of Polyurethane – Oil Palm (PolyOP) Empty Fruit Bunch composite as a microwave dielectric substrate was tested by fabricating microstrip patch antenna on it. The performance of fabricated patch antenna was measured using Vector Network Analyzer (VNA) and is compared with simulation results obtained from High Frequency Structure Simulator (HFSS) simulator. The difference of percentage in resonant frequency, return loss, bandwidth and VSWR between simulation and measurement were found to be 0.4%, 75.2%, 67.9%, and 12.7%, respectively.
本文研究了由完全可生物降解材料制成的微带贴片天线的性能。作为粘合剂的聚氨酯聚合物树脂是用从棕榈油中提取的多元醇制成的,而主复合材料是用油棕空果束纤维制成的。通过在其上制作微带贴片天线,测试了聚氨酯-油棕(PolyOP)空果束复合材料作为微波介质基底的性能。使用矢量网络分析仪(VNA)测量了制作的贴片天线的性能,并将其与高频结构模拟器(HFSS)的模拟结果进行了比较。结果发现,模拟和测量结果在谐振频率、回波损耗、带宽和驻波比方面的百分比差异分别为 0.4%、75.2%、67.9% 和 12.7%。
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引用次数: 0
The Effect of Lotus Root Starch Content on the Water Barrier Properties and Biodegradability of Cassava Bioplastic Films 莲藕淀粉含量对木薯生物塑料薄膜阻水性能和生物降解性的影响
Pub Date : 2024-02-22 DOI: 10.4028/p-29ugkz
Muhammad Iezwan Izuddin Abdullah, Wan Zarina Wan Mohamed
Biodegradable films demand increases due to the awareness of the environmental effects of synthetic plastics. However, biodegradable films based on starch have high water sensibility and poor mechanical properties. This led to an interest among the scientist in improving the properties of biodegradable films. The objectives of this study were to investigate the effect of lotus root starch content on the water solubility, water absorption, water vapor permeability and biodegradability of cassava bioplastic films. The lotus root starch was added at 10%, 20%, 30%, 40% and 50% of cassava starch. The results showed that the water absorption properties decreased by 122% to 21% and the water vapor permeability showed a decreasing trend as the lotus starch content increased. The water solubility increased from 4% to 36% with the increase of lotus starch content and biodegradability increased by 87.5% at 50% of lotus starch content. The results exposed the potential of cassava/ lotus starch bioplastic films for food packaging applications.
由于人们意识到合成塑料对环境的影响,对生物降解薄膜的需求不断增加。然而,基于淀粉的生物降解薄膜具有较高的水敏性和较差的机械性能。这引起了科学家们对改善生物降解薄膜性能的兴趣。本研究的目的是调查莲藕淀粉含量对木薯生物塑料薄膜的水溶性、吸水性、水蒸气渗透性和生物降解性的影响。莲藕淀粉的添加量分别为木薯淀粉的 10%、20%、30%、40% 和 50%。结果表明,随着莲藕淀粉含量的增加,吸水性下降了 122% 至 21%,水蒸气渗透性呈下降趋势。随着莲子淀粉含量的增加,水溶性从 4% 增加到 36%,当莲子淀粉含量为 50%时,生物降解性增加了 87.5%。这些结果揭示了木薯/莲子淀粉生物塑料薄膜在食品包装应用方面的潜力。
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引用次数: 0
Dissolving Pulp from Sansevieria Trifasciata Fiber Processed with Water-Pre-Hydrolysis, Soda-Anthraquinone Cooking and Clorine Free Bleaching 采用水预水解、苏打-蒽醌蒸煮和无氯漂白工艺加工的三叶草纤维溶解纸浆
Pub Date : 2024-02-22 DOI: 10.4028/p-1p8sdj
Yusnimar Yusnimar, Khairat Khairat, Drastinawati Drastinawati, C. Chairul, Syamsu Herman, S. Ramadhana
For a long time, rayon has been produced using dissolving pulp (DP). DP is typically made from wood or cotton, but it takes a long time to collect wood, and high-quality cotton must be imported from afar. Sansevieria trifasciata (ST) fiber, which contains more than 50% cellulose, offers potential as a raw material and a substitute for cotton and wood. It is simple to develop and grow. It can endure a wide range of light and temperature conditions. By using the water-pre-hydrolysis, soda-Anthraquinone cooking (soda-AQ), and elementary-chlorine-free (ECF) bleaching sequences, this work aims to convert ST into DP. Results, The DP was produced with a yield of 43.69%, a kappa value of 4.73, a viscosity of 9.3 cP, an alpha-cellulose content of 97.7% and a brightness of 90.7%, which was higher than the ISO brightness of 88%. The DP quality corresponds to the minimum DP level for rayon according to the Indonesian National Standard (SNI). It is very promising for further development, such as being used for viscose fiber production.
长期以来,人造丝的生产一直使用溶解浆(DP)。溶解浆通常由木材或棉花制成,但采集木材需要很长时间,而且必须从远处进口优质棉花。Sansevieria trifasciata(ST)纤维含有 50% 以上的纤维素,具有作为原材料和棉花及木材替代品的潜力。它的开发和种植都很简单。它能承受各种光照和温度条件。通过使用水预水解、苏打-蒽醌蒸煮(苏打-AQ)和无元素氯漂白(ECF)程序,本研究旨在将 ST 转化为 DP。结果发现,生产出的 DP 产率为 43.69%,卡帕值为 4.73,粘度为 9.3cP,α-纤维素含量为 97.7%,白度为 90.7%,高于国际标准化组织规定的 88%。DP 质量符合印尼国家标准(SNI)规定的人造丝最低 DP 水平。它很有希望进一步发展,例如用于粘胶纤维的生产。
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引用次数: 0
Intensify Biodegradation Process of Polylactic Acid (PLA) Waste Generated from 3D Printing Activities 强化 3D 打印活动产生的聚乳酸 (PLA) 废弃物的生物降解过程
Pub Date : 2024-02-22 DOI: 10.4028/p-m2eeip
Muhammad Naqib Hamdan, Amir Mustaqim Mohd Naim, Nuradlyna Safyah Mohd Rozi, Mohd Shaiful Sajab, H. Kaco
Additive manufacturing, or 3D printing, is a key technology driving Industry 4.0. via the formation of three-dimensional objects from a computer-aided design model which can be done through layer-by-layer technique. Polylactic acid (PLA) ranks as one of the most favored materials as a 3D printing filament. Despite its unique properties, PLA took about 12 weeks to biodegrade which is slow degradation leads to an increased rate of plastic pollution in the environment. The aim of this study was to provide an alternative method for bioplastic waste management through biodegradation process using potting mix soil at different incubation temperatures and times. The PLA was designed in coupon shapes and eventually, 3D printed, respectively. Consequently, potting mix soil was prepared in a container and coupon, as all PLA samples were then planted 7 cm from the soil surface. Eventually, PLA samples were subjected to biodegradation process in the soil at 25 °C and 50 °C. Subsequently, each sample was drawn from the soil at different incubation times up to 65 days. The results show that prolong incubation time has resulted in PLA coupon losing weight up to 10.4% and 1.4% for the incubation time of 25 °C and 50 °C, respectively. Meanwhile, the physical structure has deteriorated to powder form and the fragility decreases proportionally as prolonged incubation time. Functional groups analysis showed the functional groups altered after the biodegradation process of PLA and soil. Ergo, this method can be utilized for the community to execute self-degradation of their PLA waste generated even at their own facility.
增材制造或三维打印是推动工业 4.0 的一项关键技术,它通过逐层技术将计算机辅助设计模型转化为三维物体。聚乳酸(PLA)是最受青睐的 3D 打印长丝材料之一。尽管聚乳酸具有独特的性能,但其生物降解时间约为 12 周,降解缓慢导致环境中的塑料污染率上升。本研究的目的是通过在不同的培养温度和时间下使用盆栽混合土壤的生物降解过程,为生物塑料废物管理提供一种替代方法。研究人员将聚乳酸分别设计成不同形状,并最终进行三维打印。因此,所有聚乳酸样品都被种植在距离土壤表面 7 厘米的地方,然后在容器和试样中制备盆栽混合土壤。最后,聚乳酸样品在 25 ℃ 和 50 ℃ 的土壤中进行生物降解。随后,在不同的培养时间(最长 65 天)从土壤中提取每个样品。结果表明,在 25 ℃ 和 50 ℃ 的培养条件下,培养时间延长会导致聚乳酸脆片的重量分别减少 10.4% 和 1.4%。同时,随着培养时间的延长,物理结构退化为粉末状,脆性也成比例地降低。官能团分析表明,聚乳酸和土壤经过生物降解后,其官能团发生了变化。因此,这种方法可用于社区对其产生的聚乳酸废物进行自我降解,即使是在自己的设施中。
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引用次数: 0
Detection of Green-Synthesized Fe3O4/ Chitosan Using Spin Valve GMR Sensor with Wheatstone Bridge Circuit 利用带有惠斯通电桥电路的自旋阀 GMR 传感器检测绿色合成的 Fe3O4/ 壳聚糖
Pub Date : 2024-02-22 DOI: 10.4028/p-7ulydw
Shania Garcia, Ni’matil Mabarroh, Rona Cuana, H. Ardiyanti, N. Istiqomah, E. Suharyadi
Detection of magnetic nanoparticles (MNPS) label is essential to determine the performance of giant magnetoresistance (GMR) sensors in biosensing technology. This research identifies the potency of green-synthesized Fe3O4/Chitosan on GMR sensors, which has never been explored. MNPS label was synthesized by the coprecipitation method based on the green synthesis route because cost-effective, non-toxic, and reduces waste production. Chitosan is considered the best polymer candidate as a stabilizer of Fe3O4 because they are biodegradable, biocompatible, and hydrophilic. The characteristics of Fe3O4/Chitosan with several concentrations and the effect on sensor signals were investigated. Measurement of Fe3O4/Chitosan using a spin-valve based sensor with a Ta (2nm)/Ir20Mn80(10nm)/Co90Fe10(3nm)/Co84Fe10B4(10nm)/Ta (5nm) structure on Si/SiO2 substrate. Fe3O4/Chitosan has a spherical shape with an inverse spinel cubic structure. The crystallite sizes of Fe3O4/Chitosan (1:1) and Fe3O4/Chitosan (2:1) are 7.9 and 7.5 nm, respectively. Fourier transforms infrared spectra of Fe3O4/Chitosan showed the NH2 bending at 1560 cm−1, C-O-C stretching at 1386 cm−1, and Fe-O stretching at 580 cm−1. The results indicate that chitosan effectively coated the surface of Fe3O4. The sensitivity of the GMR sensor increased to 0.04 mV/mg/mL and 0.05 mV/mg/mL, in the case of Fe3O4/Chitosan (1:1) and Fe3O4/Chitosan (2:1). The increase in the sensitivity was caused by the decrease in diamagnetic material composition, crystallite size and the increase in the saturation magnetization of Fe3O4/Chitosan. Green-synthesized Fe3O4/Chitosan can be detected by GMR sensor by providing a low external magnetic field within the 60s and reach ruthless performance as a magnetic label to be applied to biosensors application in the future.
检测磁性纳米粒子(MNPS)标签对于确定生物传感技术中巨磁电阻(GMR)传感器的性能至关重要。本研究发现了绿色合成的 Fe3O4/Chitosan 在 GMR 传感器上的有效性,而这一点从未被探索过。MNPS 标签是通过共沉淀法合成的,该方法基于绿色合成路线,具有成本低、无毒、减少废物产生等优点。壳聚糖具有生物降解性、生物相容性和亲水性,因此被认为是作为 Fe3O4 稳定剂的最佳聚合物。研究了几种浓度的 Fe3O4/壳聚糖的特性及其对传感器信号的影响。在 Si/SiO2 基质上使用基于自旋阀的传感器测量 Fe3O4/壳聚糖,该传感器具有 Ta(2nm)/Ir20Mn80(10nm)/Co90Fe10(3nm)/Co84Fe10B4(10nm)/Ta(5nm)结构。Fe3O4/Chitosan 呈球形,具有反尖晶石立方结构。Fe3O4/Chitosan (1:1) 和 Fe3O4/Chitosan (2:1) 的晶粒大小分别为 7.9 和 7.5 nm。傅立叶变换红外光谱显示,Fe3O4/壳聚糖的 NH2 弯曲位于 1560 cm-1,C-O-C 伸展位于 1386 cm-1,Fe-O 伸展位于 580 cm-1。结果表明壳聚糖有效地包覆了 Fe3O4 表面。在 Fe3O4/壳聚糖(1:1)和 Fe3O4/壳聚糖(2:1)的情况下,GMR 传感器的灵敏度分别提高到 0.04 mV/mg/mL 和 0.05 mV/mg/mL。灵敏度的增加是由于二磁性材料成分的减少、晶体尺寸的减小以及 Fe3O4/Chitosan 饱和磁化的增加。绿色合成的 Fe3O4/Chitosan 可在 60 秒内通过 GMR 传感器提供的低外加磁场进行检测,作为一种磁性标签性能优异,未来可应用于生物传感器。
{"title":"Detection of Green-Synthesized Fe3O4/ Chitosan Using Spin Valve GMR Sensor with Wheatstone Bridge Circuit","authors":"Shania Garcia, Ni’matil Mabarroh, Rona Cuana, H. Ardiyanti, N. Istiqomah, E. Suharyadi","doi":"10.4028/p-7ulydw","DOIUrl":"https://doi.org/10.4028/p-7ulydw","url":null,"abstract":"Detection of magnetic nanoparticles (MNPS) label is essential to determine the performance of giant magnetoresistance (GMR) sensors in biosensing technology. This research identifies the potency of green-synthesized Fe3O4/Chitosan on GMR sensors, which has never been explored. MNPS label was synthesized by the coprecipitation method based on the green synthesis route because cost-effective, non-toxic, and reduces waste production. Chitosan is considered the best polymer candidate as a stabilizer of Fe3O4 because they are biodegradable, biocompatible, and hydrophilic. The characteristics of Fe3O4/Chitosan with several concentrations and the effect on sensor signals were investigated. Measurement of Fe3O4/Chitosan using a spin-valve based sensor with a Ta (2nm)/Ir20Mn80(10nm)/Co90Fe10(3nm)/Co84Fe10B4(10nm)/Ta (5nm) structure on Si/SiO2 substrate. Fe3O4/Chitosan has a spherical shape with an inverse spinel cubic structure. The crystallite sizes of Fe3O4/Chitosan (1:1) and Fe3O4/Chitosan (2:1) are 7.9 and 7.5 nm, respectively. Fourier transforms infrared spectra of Fe3O4/Chitosan showed the NH2 bending at 1560 cm−1, C-O-C stretching at 1386 cm−1, and Fe-O stretching at 580 cm−1. The results indicate that chitosan effectively coated the surface of Fe3O4. The sensitivity of the GMR sensor increased to 0.04 mV/mg/mL and 0.05 mV/mg/mL, in the case of Fe3O4/Chitosan (1:1) and Fe3O4/Chitosan (2:1). The increase in the sensitivity was caused by the decrease in diamagnetic material composition, crystallite size and the increase in the saturation magnetization of Fe3O4/Chitosan. Green-synthesized Fe3O4/Chitosan can be detected by GMR sensor by providing a low external magnetic field within the 60s and reach ruthless performance as a magnetic label to be applied to biosensors application in the future.","PeriodicalId":507742,"journal":{"name":"Materials Science Forum","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140439411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Effects of Silver Nanoparticles on the Antimicrobial and Biodegradation of Cornstarch Bioplastic 银纳米粒子对玉米淀粉生物塑料抗菌和生物降解的影响
Pub Date : 2024-02-22 DOI: 10.4028/p-vvm7a4
Rina Ningtyas, Shanaz Nadya, Muryeti Muryeti, D. Priadi, Mochamad Chalid
The development of bioplastics is currently increasing, because bioplastics are an effort to reduce landfill waste. One of the bioplastics that has good degradation ability is cornstarch. The addition of nanoparticles was carried out to improve the properties of bioplastic packaging. One example of the application of nanotechnology in food packaging is silver nanoparticles (AgNP), known as antimicrobial substances. This research was conducted to determine the effect of adding AgNP (0%, 1%, and 2%) on the antimicrobial and biodegradation of cornstarch bioplastics. Bioplastics are made by casting method. AgNP was used from the synthesis of silver nitrate (AgNO3) and trisodium citrate dihydrate (C6H5Na3O7.2H2O) as a reducing agent and stabilizer by chemical reduction method, which was then analyzed by FTIR. The results obtained showed that cornstarch bioplastic AgNP 1% has the ability to estimate the fastest degradation time among other concentrations with an addition of 103 days. Cornstarch bioplastic AgNP 2% had the best ability to inhibit bacterial growth, with antibacterial inhibition zone diameters of 11.03 mm (Staphylococcus aureus) and 10.61 mm (Escherichia coli). However, AgNP could not inhibit the mold growth of Aspergillus niger. The addition of AgNP to cornstarch bioplastics can increase the degradation capabilities and antibacterial activity of bioplastics.
目前,生物塑料的开发正在不断增加,因为生物塑料是减少垃圾填埋的一种努力。玉米淀粉是降解能力较强的生物塑料之一。为了改善生物塑料包装的性能,人们开始添加纳米粒子。纳米技术在食品包装中的一个应用实例是纳米银粒子(AgNP),它被称为抗菌物质。本研究旨在确定添加 AgNP(0%、1% 和 2%)对玉米淀粉生物塑料的抗菌性和生物降解性的影响。生物塑料是通过浇铸法制成的。采用化学还原法合成硝酸银(AgNO3)和二水柠檬酸三钠(C6H5Na3O7.2H2O)作为还原剂和稳定剂,然后用傅立叶变换红外光谱分析 AgNP。结果表明,玉米淀粉生物塑料 AgNP 1% 的降解时间在其他浓度中最快,为 103 天。玉米淀粉生物塑料 AgNP 2% 抑制细菌生长的能力最强,抗菌抑菌区直径分别为 11.03 毫米(金黄色葡萄球菌)和 10.61 毫米(大肠杆菌)。不过,AgNP 无法抑制黑曲霉的霉菌生长。在玉米淀粉生物塑料中添加 AgNP 可提高生物塑料的降解能力和抗菌活性。
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引用次数: 0
Impact Resistance Enhancement of GLARE Composite Laminates Reinforced with Shape Memory Alloy Wires 用形状记忆合金丝增强 GLARE 复合材料层压板的抗冲击性能
Pub Date : 2024-02-22 DOI: 10.4028/p-9wdbiu
Yudha Arya Sumbaga, Rahmat Saptono
This study investigates the impact resistance of Glass Laminate Aluminum Reinforced Epoxy (GLARE) composite laminates by incorporating shape memory alloy (SMA) wires. The influence of varying percentages of pre-strain (0%, 1%, 3%, and 5%) on the SMA wires embedded in the GLARE composites was examined. Laminate composites were made by hand lay-up method using 1100 series aluminum, glass laminate, epoxy resin, and nitinol wire. Impact testing was carried out using the Charpy (un-notched) method. The results demonstrate that the presence of SMA wires significantly enhances the impact resistance of the laminates. The energy absorption capacity of the laminates was found to increase with increasing pre-strain percentage. The highest impact resistance was observed in the specimens with 3% pre-strain, which exhibited a 35.2% increase in energy absorption compared to the specimens without SMA wires. However, a further increase in pre-strain to 5% resulted in a 21.5% decrease in energy absorption due to the higher fraction of stress-induced martensite, limiting the shape memory effect. Additionally, the damage analysis revealed that the absence of SMA wires led to severe debonding and delamination in the GLARE laminates. Conversely, specimens with 3% pre-strain exhibited the least damage, with limited debonding observed only in the front interface of the aluminum and epoxy-laminated fiberglass layers. The higher damage resistance of these specimens is attributed to their optimal energy absorption capability. Based on the findings, it is recommended to further investigate alternative shape memory alloy materials to determine their impact resistance enhancement potential compared to the current SMA wires. Additionally, conducting experiments with pre-strain percentages in the range of 3-5% would provide a better understanding of the maximum achievable performance. Furthermore, microscale observations should be conducted to gain more detailed insights into the damage mechanisms of the tested specimens.
本研究探讨了玻璃层压铝增强环氧树脂(GLARE)复合材料层压板中加入形状记忆合金(SMA)丝后的抗冲击性能。研究了不同比例的预应变(0%、1%、3% 和 5%)对嵌入 GLARE 复合材料中的 SMA 线的影响。层压复合材料是用 1100 系列铝、玻璃层压板、环氧树脂和镍钛诺丝通过手糊法制成的。冲击测试采用夏比(无缺口)法进行。结果表明,SMA 线的存在大大增强了层压板的抗冲击能力。层压板的能量吸收能力随着预应变百分比的增加而增加。预应变为 3% 的试样抗冲击能力最强,与不含 SMA 线的试样相比,能量吸收能力提高了 35.2%。然而,预应变进一步增加到 5%后,由于应力诱导马氏体的比例增加,限制了形状记忆效应,能量吸收降低了 21.5%。此外,损伤分析表明,没有 SMA 线会导致 GLARE 层压板严重脱粘和分层。相反,预应变为 3% 的试样损伤最小,仅在铝层和环氧树脂层玻璃纤维层的前端界面观察到有限的脱粘现象。这些试样具有较高的抗破坏性,这是因为它们具有最佳的能量吸收能力。根据研究结果,建议进一步研究替代的形状记忆合金材料,以确定与当前的 SMA 金属丝相比,它们的抗冲击增强潜力。此外,在预应变百分比为 3-5% 的范围内进行实验将有助于更好地了解可实现的最大性能。此外,还应进行微观观察,以便更详细地了解测试试样的损坏机制。
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引用次数: 0
Synthesis and Characterization of AuNP/TiO2 Hybrid Nanoparticles for Possible Photocatalytic Application 可用于光催化应用的 AuNP/TiO2 混合纳米粒子的合成与表征
Pub Date : 2024-02-15 DOI: 10.4028/p-ogeu80
Jay C. Dulog, Romnick B. Unabia, Jared Deve P. Delicana, Aldrin Lalem, Noel Lito B. Sayson, R. Capangpangan, A. Lubguban, Arnold A. Alguno
Nanoparticles have been intensively studied due to their unique, size-dependent properties, paving the way for various applications, particularly in photocatalysis. This study aims to determine the physicochemical characteristics of TiO2 and Au nanoparticles and the AuNP/TiO2 hybrid nanoparticles. Employing multiple characterization techniques, the structural and functional parameters were elucidated. The Brunauer-Emmett-Teller (BET) surface area analysis revealed the pore sizes of TiO2 and the Au/TiO2 hybrid nanoparticles as 12 nm and 18 nm, respectively. The Dynamic light scattering (DLS) measurements revealed the hydrodynamic size of the AuNP/TiO2 hybrid nanoparticles at 386 nm. The UV-visible spectroscopy showed the absorbance peaks associated with their electronic structures and potential photocatalytic applications. The fast Fourier infrared (FTIR) spectroscopy results revealed the surface molecular interactions crucial for nanoparticle functionalities. The AuNP/TiO2 hybrid nanoparticles exhibit a larger pore size compared to TiO2NPs, indicating their superior adsorption capability. Moreover, the unique band gap of TiO2NPs and electron-hole pair generation make it a formidable candidate for photocatalysis. The incorporation of AuNPs may further augment charge separation, optimizing photocatalytic activity. These findings spotlight the promise of these AuNP/TiO2 hybrid nanoparticles in possible photocatalytic applications.
纳米粒子因其独特的、与尺寸有关的特性而受到深入研究,为各种应用,尤其是光催化应用铺平了道路。本研究旨在确定 TiO2 和金纳米粒子以及 AuNP/TiO2 混合纳米粒子的物理化学特性。采用多种表征技术,阐明了其结构和功能参数。布鲁纳-艾美特-泰勒(BET)表面积分析表明,TiO2 和 Au/TiO2 混合纳米粒子的孔径分别为 12 nm 和 18 nm。动态光散射(DLS)测量显示 AuNP/TiO2 混合纳米粒子的流体力学尺寸为 386 纳米。紫外-可见光谱显示了与其电子结构和潜在光催化应用相关的吸光峰。快速傅立叶红外光谱(FTIR)结果显示了对纳米粒子功能至关重要的表面分子相互作用。与 TiO2NPs 相比,AuNP/TiO2 混合纳米粒子的孔径更大,表明其吸附能力更强。此外,TiO2NPs 独特的带隙和电子-空穴对生成使其成为光催化的有力候选材料。AuNPs 的加入可进一步增强电荷分离,优化光催化活性。这些发现凸显了这些 AuNP/TiO2 混合纳米粒子在可能的光催化应用中的前景。
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引用次数: 0
Application of Green Synthesized Silver Nanoparticles for Dye Wastewater Treatment 绿色合成银纳米粒子在染料废水处理中的应用
Pub Date : 2024-02-15 DOI: 10.4028/p-uifca6
Feb Alexis P. Marquez, E. Fundador, N. G. Fundador
A facile one-pot synthesis of silver nanoparticles (AgNPs) was achieved using the ethanolic extract of Cavendish banana florets as source of reducing agents for the conversion of Ag+ to Ag. The appearance of surface plasmon resonance peak between 410–435 nm in the UV Vis spectra confirmed the formation of AgNPs. The effects of different reaction conditions on the size and concentration of AgNPs were evaluated. The optimum conditions identified were pH 7 at 80 °C. Transmission electron microscopy (TEM) revealed spherical AgNPs with a mean particle size of 13.55 nm. On the other hand, energy-dispersive X-ray (EDX) analysis confirmed the presence of silver (Ag) as the bulk element (87.25%). Other elements such as carbon (C) and oxygen (O) are attributed to the capping agents of AgNPs which agrees with the results in the Fourier-transform infrared spectroscopy (FTIR) analysis. The optimized AgNPs were used for dye degradation using methyl orange (MO) as the model dye under acidified conditions. The maximum MO dye degradation of 96.07% and 77.32% at pH 1.5 and 2 were achieved after 10 min and 1320 min, respectively. This highlights the potential use of green-synthesized AgNPs for dye wastewater treatment.
以卡文迪许香蕉小花的乙醇提取物为还原剂来源,实现了银纳米粒子(AgNPs)的简单一锅合成。紫外可见光谱在 410-435 纳米之间出现的表面等离子共振峰证实了 AgNPs 的形成。评估了不同反应条件对 AgNPs 尺寸和浓度的影响。确定的最佳条件是 pH 值为 7,温度为 80 °C。透射电子显微镜(TEM)显示,AgNPs 呈球形,平均粒径为 13.55 nm。另一方面,能量色散 X 射线(EDX)分析证实银(Ag)是主要元素(87.25%)。其他元素如碳(C)和氧(O)被认为是 AgNPs 的封端剂,这与傅立叶变换红外光谱(FTIR)分析的结果一致。在酸化条件下,以甲基橙(MO)为模型染料,使用优化的 AgNPs 进行染料降解。在 pH 值为 1.5 和 2 的条件下,分别经过 10 分钟和 1320 分钟后,MO 染料的降解率分别达到 96.07% 和 77.32%。这凸显了绿色合成的 AgNPs 在染料废水处理中的潜在用途。
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