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Biodegradation assessment of polythene by microalgae growing on polythene debris from fresh water bodies 微藻生长在淡水水体聚乙烯碎片上对聚乙烯的生物降解评价
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-03-12 DOI: 10.1007/s13726-025-01475-1
Mamta Sharma, Ameeta Sharma, Neha Batra, Arvind Pareek

Polythene is exceedingly harmful to the environment and living organisms because of its incredibly slow rate of breakdown. The biological method of polythene degradation has arisen as an eco-beneficial solution to the global problem of plastic pollution, as the conventional methods of polythene degradation, including as incineration, land filling, and chemical treatment, have proven to be detrimental for the environment. In addition to being economical, biological deterioration is environmentally benign. Various microbes like fungi, algae and bacteria have been tested for degradation of polythene in natural niche, with lesser work on microalgae. This research work is being carried out with the objective to assess the degradation of polythene with microalgae application. Ten different algal species were isolated and identified from algal growth on polythene bags, collected from the three different water waste sites in Kota, India. The isolated algal strains were grown and cultured in BG-11 broth before being assessed for their capabilities to biologically degrade biodegradable polythene, low density polythene (LDPE) and high density polythene (HDPE) sheets. The polythene sheets were treated with the algal isolates and incubated for a month before being assessed for degradation. These biologically treated samples were later analyzed for weight loss. Further investigations were also performed through FTIR and SEM to analyze the changes in morphological and chemical characteristics of the biodegradable polythene samples. Bestowing to SEM micrographs, microalgae could adhere and colonize plastics resulting in its phycodegradation. This hitherto reports that among the isolated algae only Oocystis solitaria, Phormidium tenue and Scenedesmus carinatus possessed the high capabilities to degrade the polyethylene samples.

Graphical Abstract

聚乙烯对环境和生物体极其有害,因为它的分解速度极其缓慢。由于传统的聚乙烯降解方法,包括焚烧、填埋和化学处理,已被证明对环境有害,因此,生物降解聚乙烯的方法已成为解决全球塑料污染问题的一种生态有益的解决方案。除了经济之外,生物退化对环境也是无害的。各种微生物,如真菌、藻类和细菌,已经测试了在自然生态位中降解聚乙烯的能力,而对微藻的研究较少。这项研究工作的目的是评价微藻对聚乙烯的降解作用。从印度哥打三个不同的污水场收集的塑料袋上的藻类生长中分离和鉴定了10种不同的藻类。分离的藻类菌株在BG-11肉汤中生长培养,然后评估其生物降解可生物降解聚乙烯、低密度聚乙烯(LDPE)和高密度聚乙烯(HDPE)片的能力。用海藻分离物处理聚乙烯片,并在进行降解评估之前孵育一个月。这些经过生物处理的样品随后被分析以减轻体重。通过FTIR和SEM分析了生物降解聚乙烯样品的形态和化学特征的变化。扫描电镜显示,微藻可以附着并定植塑料,导致塑料降解。迄今为止,在分离的藻类中,只有卵囊藻(Oocystis solitaria)、Phormidium tenue和Scenedesmus carinatus具有较高的降解聚乙烯样品的能力。图形抽象
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引用次数: 0
Comparative analysis of nanocellulose extraction from Cocos nucifera shell by ultrasonication versus acid hydrolysis for methylene blue dye removal 超声法提取椰壳纳米纤维素与酸水解法去除亚甲基蓝染料的比较分析
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-03-11 DOI: 10.1007/s13726-025-01462-6
Fatimah Azzahra’ Che Saupi, Nor Saadah Mohd Yusof, Vetrimurugan Rajagopal, Nor Mas Mira Abd Rahman

The present study explores an innovative approach to extract nanocellulose from Cocos nucifera shells using ultrasound-assisted extraction and acid hydrolysis methods, comparing yield, efficiency, chemical changes, thermal stability, crystallinity, and morphologic properties. Various analytical techniques, including ATR-FTIR, TGA, XRD, FESEM, and TEM, were employed to evaluate each method. Optimization of ultrasonication and acid hydrolysis parameters such as amplitude power, sonication time, acid concentration, and reaction duration was conducted. Nanocellulose produced via ultrasonication at 70% amplitude exhibited a spherical shape with an average particle size of 2.51 nm, similar to acid-hydrolyzed nanocellulose (ANC) obtained using 65% sulfuric acid. Ultrasound-assisted nanocellulose (UNC) demonstrated enhanced thermal stability, while ANC achieved a higher crystallinity index, reaching 72.1% compared to 67.5% for UNC. In addition, this study is among the first to directly compare the adsorption capabilities of nanocellulose extracted by ultrasound and acid hydrolysis for methylene blue (MB) dye removal, addressing a critical need in industrial wastewater treatment. UNC achieved 96.88% MB removal efficiency, approximately 6% higher than ANC. Overall, the findings highlight the effectiveness of ultrasound-assisted extraction in producing nanocellulose with high surface area and strong adsorption properties, paving the way for a greener and more efficient alternative to conventional acid hydrolysis in nanocellulose production and wastewater treatment.

Graphical abstract

本研究探索了一种利用超声辅助提取法和酸水解法从椰壳中提取纳米纤维素的创新方法,比较了产率、效率、化学变化、热稳定性、结晶度和形态性质。采用ATR-FTIR、TGA、XRD、FESEM和TEM等分析技术对每种方法进行了评价。对超声和酸水解的振幅功率、超声时间、酸浓度、反应时间等参数进行了优化。在70%振幅下,超声法制备的纳米纤维素呈球形,平均粒径为2.51 nm,与65%硫酸法制备的酸水解纳米纤维素(ANC)相似。超声辅助纳米纤维素(UNC)表现出更强的热稳定性,而ANC的结晶度指数达到72.1%,而UNC的结晶度指数为67.5%。此外,本研究是第一个直接比较超声提取纳米纤维素和酸水解提取纳米纤维素对亚甲基蓝(MB)染料的吸附能力的研究,解决了工业废水处理中的一个关键需求。UNC对MB的去除率达到96.88%,比ANC高出约6%。总的来说,这些发现强调了超声辅助提取在生产具有高表面积和强吸附性能的纳米纤维素方面的有效性,为在纳米纤维素生产和废水处理中替代传统酸水解的更环保、更有效的替代方法铺平了道路。图形抽象
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引用次数: 0
Nature-derived otolith loaded polyethylene glycol-polycaprolactone electrospun composite nanofiber membranes: preparation, characterization, and biocompatibility evaluation 天然来源的耳石负载聚乙二醇-聚己内酯静电纺复合纳米纤维膜:制备、表征和生物相容性评价
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-03-10 DOI: 10.1007/s13726-025-01473-3
Sibel Selçuk Pekdemir, Kübra Karadaş Gedik, Ali Kuruçay, Hatice Onay, Ahmet Ulu, Mustafa Ersin Pekdemir, Seda Kolak, Göktuğ Dalgıç, Burhan Ateş

The electrospun nanofibers have paid much attention to biomedical applications. In this study, the electrospun composite nanofibers were prepared based on optimized polycaprolactone (PCL, 12 wt%) and polyethylene glycol (PEG, 3.6 wt%) polymers loaded with otoliths particles (OTO, 10–30 wt%) by electrospinning technique. The morphological, molecular interactions, crystallinity, and thermal properties of the composite nanofiber membranes were characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry. In addition to that, swelling behaviors, biodegradability, porosity, and biocompatibility were also evaluated. Both PEG/PCL and OTO/PEG/PCL nanofibers revealed bead-less constructions with average diameters of around 500 nm. Thermogravimetric analysis revealed OTO/PEG/PCL composite membranes thermally stable up to 300 °C. XRD results also indicated a good crystallinity for the OTO/PEG/PCL composite membranes due to higher crystallinity of otolith. Adding otolith to PEG/PCL nanofibers did not obviously change the water uptake capacity, biodegradability, and porosity while increasing swelling ratio. Finally, membranes with the lowest otolith concentration (10% w/w) showed 96.2% cell viability, while increasing otolith concentration decreased cell viability. Based on the obtained results, the cytotoxicity of OTO/PEG/PCL membranes was evaluated with mouse fibroblast (L-929) cells by more than 85% survival during 72 h, which revealed that the OTO/PEG/PCL membranes were non-toxic. Taken together, these data suggest that OTO/PEG/PCL membranes could potentially be used as a nanofiber scaffold for applications.

Graphical abstract

静电纺丝纳米纤维在生物医学上的应用备受关注。本研究以优化后的聚己内酯(PCL, 12 wt%)和聚乙二醇(PEG, 3.6 wt%)聚合物为载体,负载10-30 wt%的耳石颗粒(OTO, 10-30 wt%),采用静电纺丝技术制备了电纺复合纳米纤维。利用扫描电镜、傅里叶变换红外光谱、x射线衍射、热重分析和差示扫描量热法对复合纳米纤维膜的形态、分子相互作用、结晶度和热性能进行了表征。此外,还对膨胀行为、可生物降解性、孔隙度和生物相容性进行了评价。PEG/PCL和OTO/PEG/PCL纳米纤维均显示出平均直径约500 nm的无头结构。热重分析表明OTO/PEG/PCL复合膜的热稳定性可达300°C。XRD结果还表明,由于耳石的结晶度较高,OTO/PEG/PCL复合膜具有良好的结晶度。在PEG/PCL纳米纤维中添加耳石对吸水能力、生物降解性和孔隙率没有明显影响,但增加了溶胀率。最后,耳石浓度最低(10% w/w)的膜细胞存活率为96.2%,而耳石浓度增加则会降低细胞存活率。在此基础上,用小鼠成纤维细胞(L-929)对OTO/PEG/PCL膜进行了细胞毒性评价,72 h存活率超过85%,结果表明OTO/PEG/PCL膜无毒。综上所述,这些数据表明OTO/PEG/PCL膜有可能作为纳米纤维支架应用。图形抽象
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引用次数: 0
Catalytic action of natural clay on polyolefins during reactive processing 反应过程中天然粘土对聚烯烃的催化作用
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-03-08 DOI: 10.1007/s13726-025-01474-2
Emerson Ferreira da Silva, Denise dos Santos Luiz, Antonio José de Andrade Junior, Clodoaldo Saron

Natural and modified clays based on the montmorillonite structure are widely used for the preparation of polymer composites and nanocomposites. However, these clays can also cause changes in the properties of the polymer matrix after thermal treatment. The aim of the present study was to evaluate the changes in structure and properties of linear low-density polyethylene (LLDPE), polypropylene (PP) and LLDPE/PP blend after thermomechanical processing on high shear rate and controlled atmosphere in the presence of natural clay. Thus, natural bentonite clay in powder form was previously incorporated at 5 wt% to the LLDPE, PP and LLDPE blend in the proportion 70/30 wt%, respectively. Afterward, the materials were processed in an internal mixer MH-600 at 4500 rpm under nitrogen flow, maintaining the shearing by 90 s after polymer melting. Clay caused severe changes in the rheological, thermal and mechanical properties of the polymers, mainly for PP and LLDPE/PP blends, increasing the melt flow rate by 400% and decreasing elongation-at-break to 20% of the initial values. The presence of tertiary carbon in polymer chains of PP should lead to a higher sensibility to the degradation, showing that the stability of the polymer determines the structural changes in the materials. The use and control of these changes can be useful for the processing and compatibilization of complex polymer mixtures, such as polymer waste during mechanical recycling operations. On the other hand, in addition to the reinforcement action, the catalytic and deleterious effects of the clays should also be considered for the preparation of polymer composites.

Graphical abstract

基于蒙脱土结构的天然粘土和改性粘土被广泛用于制备高分子复合材料和纳米复合材料。然而,这些粘土在热处理后也会引起聚合物基体性质的变化。本文研究了线性低密度聚乙烯(LLDPE)、聚丙烯(PP)和LLDPE/PP共混物在天然粘土的存在下,在高剪切速率和可控气氛下进行热机械加工后的结构和性能变化。因此,在LLDPE、PP和LLDPE共混物中,以5 wt%的比例分别以70/30 wt%的比例加入粉状的天然膨润土粘土。然后将材料放入MH-600内混机中,在氮气流下以4500转/分的速度进行加工,在聚合物熔化后保持剪切90 s。粘土使聚合物的流变学、热学和力学性能发生了严重变化,主要是PP和LLDPE/PP共混物,熔体流动速率提高了400%,断裂伸长率降低到初始值的20%。PP聚合物链中叔碳的存在应该会导致对降解的更高敏感性,表明聚合物的稳定性决定了材料的结构变化。这些变化的使用和控制对于复杂聚合物混合物的处理和增容是有用的,例如在机械回收操作期间的聚合物废物。另一方面,在制备聚合物复合材料时,除了增强作用外,还应考虑粘土的催化和有害作用。图形抽象
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引用次数: 0
Cellulose nanocrystals effect to improve mechanical properties of epoxy-based glass fiber-reinforced composites 纤维素纳米晶对提高环氧基玻璃纤维增强复合材料力学性能的影响
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-03-04 DOI: 10.1007/s13726-025-01468-0
Alaa Mohemmed Salih, Farid Vakili-Tahami, Hasan Biglari

This work investigated the effect of incorporating cellulose nanocrystals (CNCs) into epoxy resin to enhance the mechanical properties of the glass fiber-reinforced polymer (GFRP) nanocomposites, with the goal of identifying the optimal CNC content based on mechanical and thermal performance. CNCs obtained via acid hydrolysis were added in varying weight percentages (0.5, 1, and 1.5 wt%) to the epoxy resin. The formation of molecular bonds between CNCs and epoxy resin was confirmed through Fourier-transform infrared (FTIR) and Raman spectroscopy methods. Results revealed that the addition of 1 wt% CNCs notably enhanced the mechanical properties, including a 24% increase in tensile strength and 25% improvement in elastic modulus compared to the neat epoxy sample. Scanning electron microscopy (SEM) further demonstrated improved adhesion between glass fibers and epoxy at this concentration, attributing enhanced interfacial bonding to the hydrogen interactions between CNCs and glass fibers. The highest CNC content of 1.5 wt% resulted in agglomeration, leading to a moderate reduction in mechanical properties. However, this sample with a 30% improvement still exhibited a higher modulus than the neat epoxy due to restricted chain mobility. The thermal analysis showed an increase of 4.5 °C in glass transition temperature in the 1.5 wt% CNC/epoxy-based GFRP composite sample. The findings suggested that CNCs significantly improved the mechanical and thermal performance of the GFRP/CNCs-epoxy nanocomposites, making them promising for high-performance applications in aerospace, automotive, and construction industries.

Graphical abstract

本文研究了在环氧树脂中加入纤维素纳米晶体(CNC)以增强玻璃纤维增强聚合物(GFRP)纳米复合材料的机械性能,目的是根据机械和热性能确定最佳CNC含量。通过酸水解得到的cnc以不同的重量百分比(0.5,1和1.5 wt%)添加到环氧树脂中。通过傅里叶变换红外(FTIR)和拉曼光谱方法证实了cnc与环氧树脂之间形成的分子键。结果表明,与纯环氧样品相比,添加1 wt%的cnc显著提高了机械性能,包括抗拉强度提高24%,弹性模量提高25%。扫描电子显微镜(SEM)进一步证明,在这种浓度下,玻璃纤维和环氧树脂之间的附着力得到改善,这归因于cnc和玻璃纤维之间的氢相互作用增强了界面键合。最高的CNC含量为1.5 wt%,导致结块,导致机械性能的适度降低。然而,由于链迁移率受限,该样品的模量比纯环氧树脂高30%。热分析表明,在1.5%的CNC/环氧基GFRP复合材料样品中,玻璃化转变温度提高了4.5℃。研究结果表明,cnc显著提高了GFRP/ cnc -环氧纳米复合材料的机械和热性能,使其在航空航天、汽车和建筑行业的高性能应用前景广阔。图形抽象
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引用次数: 0
Morphological predictions of polyurethane/clay nanocomposite systems by compressible self-consistent field theory 基于可压缩自洽场理论的聚氨酯/粘土纳米复合材料体系形态预测
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-02-28 DOI: 10.1007/s13726-025-01467-1
Gohar Mohammadi, Somayeh Ghasemirad, Mehrdad Kokabi

Thermodynamic modelling was conducted using compressible self-consistent field theory to predict the morphology of polyurethane (PU)/clay nanocomposites. The PU comprised of poly(tetramethylene ether)glycol, as its soft segment, and methylene bis(cyclohexyl) diisocyanate-butanediol-methylene bis(cyclohexyl) diisocyanate, as its hard segment. The effect of polyol molecular weight, degree of polymerization of PU, nanoparticle volume fraction, solubility parameter of nanoparticle, and temperature on the free energy of the system was investigated. At 25 °C, a tenfold increase in the molecular weight of the polyol from 1000 to 10,000 g/mol in a PU nanocomposite containing clay with a solubility parameter of 24.4 (J/cm3)1/2 at a volume fraction of 0.05 led to 56% drop in the free energy per unit area of the system. In similar conditions regarding temperature and the solubility parameter of clay, with a fivefold increase in the polymerization degree of a PU comprised of a polyol with a molecular weight of 1000 g/mol, from 10 to 50, a 110% reduction in the free energy per unit area was observed. Raising the nanoparticle volume fraction from 0.05 to 0.1 and reducing the solubility parameter of the nanoparticle from 24.4 to 17.7 (J/cm3)1/2 decreased the free energy per unit area. Furthermore, with an increase in the temperature from 25 to 190 °C and thus, with the thermal expansion of the polymer and the dilution of their interactions with the nanoparticle, the free energy per unit area increased. The results showed an ordered exfoliated morphology for the nanocomposite systems, in good agreement with the experimental results.

Graphical abstract

采用可压缩自洽场理论建立热力学模型,对聚氨酯/粘土纳米复合材料的形貌进行预测。聚氨酯的软段为聚四甲基醚乙二醇,硬段为亚甲基双(环己基)二异氰酸酯-丁二醇-亚甲基双(环己基)二异氰酸酯。考察了多元醇分子量、聚氨酯聚合度、纳米颗粒体积分数、纳米颗粒溶解度参数、温度等因素对体系自由能的影响。在25℃条件下,当体积分数为0.05时,含粘土的PU纳米复合材料中多元醇的分子量从1000增加到10000 g/mol,增加了10倍,其单位面积的自由能下降了56%。在温度和粘土溶解度参数相同的条件下,由分子量为1000 g/mol的多元醇组成的PU的聚合度增加5倍,从10提高到50,单位面积自由能降低110%。将纳米颗粒的体积分数从0.05提高到0.1,将纳米颗粒的溶解度参数从24.4降低到17.7 (J/cm3)1/2,降低了单位面积的自由能。此外,随着温度从25°C增加到190°C,聚合物的热膨胀和它们与纳米颗粒相互作用的稀释,单位面积的自由能增加。结果表明,纳米复合体系具有有序的剥离形貌,与实验结果吻合较好。图形抽象
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引用次数: 0
Poly(lactic acid)/saponite grafted polystyrene composites films: ultraviolet aging, enzymatic degradation behavior, and molecular dynamics simulation analysis 聚乳酸/皂土接枝聚苯乙烯复合薄膜:紫外老化、酶降解行为及分子动力学模拟分析
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-02-27 DOI: 10.1007/s13726-025-01470-6
Zhe Wang, Tengfei Shao, Yikelamu Jilili, Yumiao Ma, Weijun Zhen

The aim of this study was to compare the UV aging and enzymatic degradation behavior of pure PLA film (PLA0) and modified saponite composite (PLA3) film at 0.5% (by wt). Polarized microscopy tests showed that the addition of a modified saponite (SAP-g-PS) significantly increased the crystallization rate of the PLA films. The growth rate of spherical crystals of PLA3 composites film was 1.52 μm/min, which was much lower than that of PLA0 films. The elongation-at-break and tensile strength of the PLA3 composite films decreased from 94.03% and 33.24 MPa to 50.59% and 20.38 MPa during UV aging. However, the elongation-at-break and tensile strength of PLA0 film was decreased to 12.53% and 25.12 MPa. The carbonyl index results showed that PLA0 film was reduced from 1.86 to 1.51, and PLA3 was reduced from 2.56 to 2.29, which proved that SAP-g-PS effectively alleviated the UV aging of PLA films. The enzymatic degradation experiments showed that the mass loss results of PLA0 film reached 40.82% at the temperature of 50℃ and the degradation time of 10 h, while the mass loss rate of PLA3 was 35.40% after degradation by proteinase K. Thermogravimetric analysis showed that even after 10 h of enzymatic degradation, the T5%, T50%, and Tend of PLA3 film were still 0.48 °C, 6.08 °C, and 8.62 °C higher than those of PLA0 film, which further indicated that SAP-g-PS was beneficial to the inhibition of the enzymatic degradation process of PLA films. The FTIR analysis results showed that the C–O–C and C=O intensities of PLA0 were lower than those of PLA3, which proved that the enzymatic degradation of PLA3 was lower than that of PLA0. Finally, molecular dynamics simulations revealed that the interaction force of the PLA-based film was increased from 355.89 to −72.32 kcal/mol, and the MSD curves showed that there was a strong force between SAP-g-PS and PLA, and also indicated that the mobility was lower.

Graphical Abstract

本研究的目的是比较纯聚乳酸膜(PLA0)和改性皂土复合膜(PLA3)在0.5%(按重量计)下的紫外老化和酶降解行为。偏光显微镜实验表明,改性皂土(SAP-g-PS)的加入显著提高了聚乳酸薄膜的结晶速率。PLA3复合薄膜的球形晶体生长速率为1.52 μm/min,远低于PLA0薄膜。复合膜的断裂伸长率和抗拉强度分别从94.03%和33.24 MPa下降到50.59%和20.38 MPa。而PLA0薄膜的断裂伸长率和拉伸强度分别下降到12.53%和25.12 MPa。羰基指数结果表明,PLA0膜从1.86降低到1.51,PLA3膜从2.56降低到2.29,证明SAP-g-PS有效缓解了PLA膜的UV老化。酶解实验表明,在温度为50℃,降解时间为10 h时,PLA0膜的质量损失率达到40.82%,而蛋白酶k降解后,PLA3的质量损失率为35.40%,热重分析表明,即使在酶解10 h后,PLA3膜的T5%、T50%和Tend仍比PLA0膜高0.48℃、6.08℃和8.62℃。进一步表明,SAP-g-PS有利于抑制PLA膜的酶降解过程。FTIR分析结果表明,PLA0的C - O - C和C=O强度低于PLA3,证明PLA3的酶解低于PLA0。分子动力学模拟结果表明,PLA膜的相互作用力从355.89 kcal/mol增加到- 72.32 kcal/mol, MSD曲线显示SAP-g-PS与PLA之间存在较强的作用力,迁移率也较低。图形抽象
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引用次数: 0
Hybrid silica–sodium lignosulfonate nanoparticles for the controlled release of azadirachtin 二氧化硅-木质素磺酸钠复合纳米颗粒控释印楝素
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-02-23 DOI: 10.1007/s13726-025-01466-2
Carlos A. Busatto, Adriano Bruzzoni, María Eugenia Taverna, Maia Lescano, Diana A. Estenoz

This study explores the preparation and characterization of hybrid silica/sodium lignosulfonate nanoparticles using a simple method designed for the controlled release of azadirachtin, a bioinsecticide derived from the neem tree. Bioinsecticides like azadirachtin are highly effective, but prone to rapid photolytic degradation, which significantly limits their efficacy and longevity in agricultural applications. By combining the robust physical and chemical stability of silica with the biodegradability, UV-absorbing, and antioxidant properties of lignin, a renewable, sustainable, and cost-effective natural polymer, this innovative hybrid nanoparticle system addresses key challenges in bioinsecticide encapsulation, protection, and sustained release. The hybrid nanoparticles exhibited distinct nanocluster formation with well-defined spherical morphologies, while increasing lignin content was found to improve nanoparticle recovery and biopolymer incorporation. Specifically, lignin incorporation at 12.5, 25, and 50 mg resulted in respective lignin contents of 13.81%, 15.71%, and 21.75% within the nanoparticles. The results of this study include an optimized azadirachtin encapsulation efficiency of 37.4% and a controlled release profile extending over 48 h, demonstrating sustained release properties well suited for agricultural applications. Furthermore, environmental toxicity assessments using Vibrio Fischeri confirmed that the formulation poses minimal risk to non-target organisms, highlighting its potential as a highly safe, effective, and eco-friendly pest management solution.

Graphical abstract

本研究探索了二氧化硅/木质素磺酸钠杂化纳米颗粒的制备和表征,采用了一种简单的方法来控制印楝素的释放,印楝素是一种从楝树中提取的生物杀虫剂。印楝素等生物杀虫剂具有很高的药效,但容易发生快速的光解降解,这极大地限制了它们在农业上的应用效果和使用寿命。通过将二氧化硅强大的物理和化学稳定性与木质素(一种可再生、可持续和具有成本效益的天然聚合物)的可生物降解性、紫外线吸收性和抗氧化性相结合,这种创新的混合纳米颗粒系统解决了生物杀虫剂封装、保护和持续释放的关键挑战。混合纳米颗粒表现出明显的纳米团簇形成,具有明确的球形形态,而增加木质素含量可以提高纳米颗粒的回收率和生物聚合物的掺入。具体来说,木质素掺入12.5、25和50 mg时,纳米颗粒中的木质素含量分别为13.81%、15.71%和21.75%。结果表明,优化后的印楝素包封率为37.4%,控释时间超过48 h,缓释性能非常适合农业应用。此外,使用费氏弧菌进行的环境毒性评估证实,该配方对非目标生物的风险最小,突出了其作为一种高度安全、有效和环保的害虫管理解决方案的潜力。图形抽象
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引用次数: 0
The effect of cutting parameters in CNC milling on mechanical properties of 3D-printed polylactic acid tensile test samples: axis speed, cutting direction and number of cutting tool teeth 数控铣削中切削参数对3d打印聚乳酸拉伸试验样品力学性能的影响:轴速、切削方向和刀具齿数
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-02-18 DOI: 10.1007/s13726-025-01463-5
Muhammed Safa Kamer

Polylactic acid (PLA) filament is the most commonly used material in three-dimensional printers produced using the fused filament fabrication method. Studies on determining and developing the mechanical properties of 3D-printed PLA materials according to printing parameters continue in the literature. The innovation of this study is to determine the optimum cutting parameters with CNC (computer numerical control) milling of the test samples to determine the real mechanical properties of 3D-printed PLA tensile test samples. For this purpose, tensile test samples were produced using PLA filament with a 3D-printer, and the side edges of the produced samples were cut with a CNC milling machine using different cutting parameters. The cutting temperature, masses, surface roughness, and hardness of the products produced with this method were measured, and SEM images were taken from the cutting surfaces. As a result, it was determined that cutting temperatures and arithmetic average roughness values increased as the feed per tooth increased. It was determined that there was a 4 ~ 5 times increase in the elongation-at-break of the tensile test samples whose side surfaces were cut with a CNC milling machine. Among the parameters that are cut with CNC milling, the 5-4-500-Cl parameter, which has the lowest cutting temperature, feed per tooth, and the lowest arithmetic average roughness value, was chosen as the most suitable parameter for PLA material milling. The tensile modulus of the test sample in the selected parameter was determined to be 2.777 GPa, tensile strength was 48.442 MPa, and elongation-at-break was 15.043%.

Graphical abstract

聚乳酸(PLA)长丝是采用熔融长丝制造方法生产的三维打印机中最常用的材料。根据打印参数确定和开发3d打印PLA材料力学性能的研究继续在文献中进行。本研究的创新之处在于通过CNC(计算机数控)铣削测试样品来确定最佳切削参数,以确定3d打印PLA拉伸测试样品的真实力学性能。为此,使用3d打印机使用PLA长丝制作拉伸测试样品,并使用不同切割参数的数控铣床切割生产样品的侧边。测量了用该方法加工的工件的切削温度、质量、表面粗糙度和硬度,并采集了切削表面的扫描电镜图像。结果表明,切削温度和算术平均粗糙度值随着每齿进给量的增加而增加。结果表明,用数控铣床对试样的侧面进行切削处理后,试样的断裂伸长率提高了4 ~ 5倍。在数控铣削切削参数中,选择切削温度最低、每齿进给量最小、算法平均粗糙度值最小的5-4-500-Cl参数作为最适合PLA材料铣削的参数。选定参数下试样的拉伸模量为2.777 GPa,抗拉强度为48.442 MPa,断裂伸长率为15.043%。图形抽象
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引用次数: 0
Interlayer hybridization effect on the mechanical properties and buckling responses of basalt/carbon/epoxy-laminated composites 层间杂化对玄武岩/碳/环氧复合材料力学性能和屈曲响应的影响
IF 2.8 3区 化学 Q3 POLYMER SCIENCE Pub Date : 2025-02-17 DOI: 10.1007/s13726-025-01465-3
Hukum Chand Dewangan, Phani Kumar Mallisetty, Palash Chowdhury, Naresh Chandra Murmu

This work explored how interlayer hybridization impacted the mechanical (tensile and flexural) and buckling characteristics of the hybrid basalt/carbon/epoxy-laminated composites. The composites were fabricated using the wet-layup technique, altering the stacking sequences of basalt (B) and carbon fibers (C) layers. Laminates with the stacking sequence: [C/C/C/C]2, [B/B/B/B]2, [C/C/B/B]S, [B/B/C/C]S and [C/B/B/C]S were fabricated. Test specimens were then prepared from each laminate, and their mechanical properties were experimentally determined using a universal testing machine (UTM). In addition, elastic properties of the composites were analyzed through micro-mechanical modeling using a representative volume element (RVE) and compared with experimental results. Findings revealed that the tensile and flexural properties of the hybrid laminates fell between those of pure carbon and basalt fiber-reinforced laminates. The critical buckling load was also experimentally measured and compared with finite element simulations conducted in ANSYS®-APDL. The work further investigated how laminate geometry (aspect ratio), boundary conditions, and fibers orientations influenced the critical buckling load. Results showed that changes in stacking sequences significantly impacted the structural performance, particularly the critical buckling load. The combination of basalt and carbon fibers in epoxy laminates enhanced the flexural load capacity by 34% and increased the critical buckling load by 47%.

Graphical abstract

本研究探讨了层间杂化如何影响玄武岩/碳/环氧复合材料的力学(拉伸和弯曲)和屈曲特性。该复合材料采用湿铺技术,改变玄武岩(B)层和碳纤维(C)层的堆叠顺序。制备了顺序为[C/C/C/C]2、[B/B/B/B]2、[C/C/B/B]S、[B/B/C]S和[C/B/B/C]S的层压板。然后从每个层压板上制备试样,并使用通用试验机(UTM)实验确定其力学性能。采用代表性体积元(RVE)进行微力学建模,分析复合材料的弹性性能,并与实验结果进行对比。结果表明,混杂层合板的拉伸和弯曲性能介于纯碳和玄武岩纤维增强层合板之间。实验测量了临界屈曲载荷,并与ANSYS®-APDL有限元模拟结果进行了比较。这项工作进一步研究了层合板的几何形状(长径比)、边界条件和纤维方向对临界屈曲载荷的影响。结果表明,堆垛顺序的变化对结构性能有显著影响,尤其是对临界屈曲载荷的影响。玄武岩与碳纤维复合环氧层合板的抗弯承载力提高了34%,临界屈曲载荷提高了47%。图形抽象
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引用次数: 0
期刊
Iranian Polymer Journal
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