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Removal of azo dyes pollutants: Photo catalyst and magnetic investigation of iron oxide-zinc sulfide nanocomposites 偶氮染料污染物的去除:氧化铁-硫化锌纳米复合材料的光催化和磁性研究
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.011
Rosa Amini, G. Nabiyouni, Saghar Jarollahi
ZnS and iron oxide nanoparticles were first synthesized via precipitation and hydrothermal methods respectively. Fe3O4/ZnS nano-composites were then prepared using precipitation method. The prepared products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared (FT-IR) spectroscopy. Vibrating sample magnetometer (VSM) was used to study the magnetic property of the products. The photo-catalytic behaviour of Fe3O4/ZnS nano-composites was evaluated using the degradation of three azo-dyes under ultraviolet light irradiation. The results illustrate super paramagnetic and ferromagnetic behaviour of Fe3O4 nanoparticles. The photo catalytic behaviour of Fe3O4/ZnS nano-composites was evaluated using the degradation of three various azo dyes under ultraviolet light irradiation. The results show that, the prepared nano-composites are applicable for magnetic and photo catalytic performance.ZnS and iron oxide nanoparticles were first synthesized via precipitation and hydrothermal methods respectively. Fe3O4/ZnS nano-composites were then prepared using precipitation method. The prepared products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared (FT-IR) spectroscopy. Vibrating sample magnetometer (VSM) was used to study the magnetic property of the products. The photo-catalytic behaviour of Fe3O4/ZnS nano-composites was evaluated using the degradation of three azo-dyes under ultraviolet light irradiation. The results illustrate super paramagnetic and ferromagnetic behaviour of Fe3O4 nanoparticles. The photo catalytic behaviour of Fe3O4/ZnS nano-composites was evaluated using the degradation of three various azo dyes under ultraviolet light irradiation. The results show that, the prepared nano-composites are applicable for magnetic and photo catalytic performance.
采用沉淀法和水热法分别合成了纳米氧化铁和纳米氧化锌。采用沉淀法制备了Fe3O4/ZnS纳米复合材料。采用x射线衍射(XRD)、扫描电镜(SEM)和傅里叶变换红外光谱(FT-IR)对产物进行了表征。用振动样品磁强计(VSM)研究了产物的磁性能。利用紫外光对三种偶氮染料的降解,考察了Fe3O4/ZnS纳米复合材料的光催化性能。结果表明,Fe3O4纳米颗粒具有超顺磁性和铁磁性。利用紫外光对三种不同的偶氮染料进行降解,考察了Fe3O4/ZnS纳米复合材料的光催化性能。结果表明,所制备的纳米复合材料具有良好的磁性和光催化性能。采用沉淀法和水热法分别合成了纳米氧化铁和纳米氧化锌。采用沉淀法制备了Fe3O4/ZnS纳米复合材料。采用x射线衍射(XRD)、扫描电镜(SEM)和傅里叶变换红外光谱(FT-IR)对产物进行了表征。用振动样品磁强计(VSM)研究了产物的磁性能。利用紫外光对三种偶氮染料的降解,考察了Fe3O4/ZnS纳米复合材料的光催化性能。结果表明,Fe3O4纳米颗粒具有超顺磁性和铁磁性。利用紫外光对三种不同的偶氮染料进行降解,考察了Fe3O4/ZnS纳米复合材料的光催化性能。结果表明,所制备的纳米复合材料具有良好的磁性和光催化性能。
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引用次数: 5
Silver-nanoparticle Supported on Nanocrystalline Cellulose using Cetyltrimethylammonium Bromide: Synthesis and Catalytic Performance for Decolorization of Dyes 十六烷基三甲基溴化铵纳米晶纤维素负载银纳米颗粒:合成及其染料脱色催化性能
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.006
Hannaneh Heidari, M. Karbalaee
We reported that the ultrasonically synthesized nanocrystalline cellulose (NCC) from microcrystalline cellulose has the capacity for use as natural and green matrices for the synthesis of silver nanoparticles. Cationic surfactant cetyltrimethylammonium bromide (CTAB) was employed as a modifier and stabilizer for NCC. The structure of as-synthesized composite (Ag/CTAB/NCC) was characterized by Fourier transform infrared spectroscopy (FT-IR); field emission scanning electron microscopy (FE-SEM); Transmission electron microscopy (TEM); Energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD). The XRD pattern confirmed the single cubic phase of Ag nanoparticles with a crystallite size of about 30 nm. The catalytic activity of Ag/CTAB/NCC has been analyzed by performing the reduction of certain toxic azo methyl orange dye (MO) (by two methods) and aromatic nitro compound of 4- nitrophenol (4-NP) in shorter time. The reduction of MO to hydrazine derivatives and 4-NP to 4-aminophenol takes place with pseudo-first-order rate constants. The reduction time regularly decreased and the rate of reduction (k) increases (3 fold) with increasing catalyst amount in method (2) (mmol NaBH4/mmol MO = 250 and 42 mg catalyst) compared to the method (1) (mmol NaBH4/mmol MO = 400 and 5 mg catalyst). The results indicated that spherical AgNPs immobilized CTAB-adsorbed NCC showed better catalytic activity and shorter reduction time towards the removal of methyl orange (k = 14.2 × 10-3 s-1, t =150 s) and 4-nitrophenol (k = 5.4 × 10-3 s-1, t = 180 s) compared with previous works that could be introduced as an effective method for the catalytic treatment of wastewater.
本文报道了由微晶纤维素超声合成的纳米晶纤维素(NCC)具有作为天然和绿色基质用于合成纳米银的能力。采用阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)作为NCC的改性剂和稳定剂。用傅里叶变换红外光谱(FT-IR)对合成的Ag/CTAB/NCC进行了结构表征;场发射扫描电镜;透射电镜;能谱(EDS)和x射线衍射(XRD)。XRD谱图证实银纳米颗粒为单立方相,晶粒尺寸约为30 nm。通过两种方法在较短时间内还原某些有毒偶氮甲基橙染料(MO)和4-硝基酚(4- np)的芳香硝基化合物,分析了Ag/CTAB/NCC的催化活性。MO还原为联氨衍生物,4-NP还原为4-氨基苯酚的过程具有准一级速率常数。方法(2)(mmol NaBH4/mmol MO = 250,催化剂42 mg)与方法(1)(mmol NaBH4/mmol MO = 400,催化剂5 mg)相比,随着催化剂用量的增加,还原时间有规律地缩短,还原速率(k)提高了3倍。结果表明,球形AgNPs固定化ctab吸附的NCC对甲基橙(k = 14.2 × 10-3 s-1, t =150 s)和4-硝基苯酚(k = 5.4 × 10-3 s-1, t = 180 s)的去除具有较好的催化活性和较短的还原时间,可作为一种有效的废水催化处理方法。
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引用次数: 1
One-Pot Hydrothermal Synthesis of Functionalized Mesoporous Silica for Effective Removal of Pb(II) Ion 一锅水热合成功能化介孔二氧化硅有效去除Pb(II)离子
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.014
Najmeh Atoub, A. Amiri, Alireza Badiei, J. Ghasemi
There is a huge scope for the removal of heavy metal ions from aqueous solutions. In this study, mesoporous silica materials, (MSMs), functionalized with (3-Mercaptopropyl) trimethoxysilane, (MPTS/MSMs), were prepared and used for adsorption of Pb(II) ions from aqueous solutions. The synthesis of MPTS/MSMs adsorbent was done using one-pot hydrothermal method by immobilizing 3-Mercaptopropyl trimethoxysilane onto mesoporous silica surface. The structure and properties of the adsorbent were explored using different techniques such as FT-IR, XRD, SEM, TEM, TGA, and N2 adsorption-desorption isotherms. The adsorption applicability of prepared nanostructure for removal of the Pb(II) ions from the aqueous solution was investigated and the results showed a good selectivity in the absorption of Pb(II) ions over other ions in aqueous solution. The effect of different parameters including the solution pH, Pb(II) concentration, sorbent amount, ion interfering effect, and the contact time onto the removal efficiency of the adsorbent was investigated systematically. The maximum adsorption efficiency (~ 97%) was found for the solutions with pH = 6, the best contact time was seen as 30 min for 50 mg L−1 of the analyte under the optimal conditions. The adsorbent was triumphantly used for the removal of Pb (II) ions from the three real water samples, including tap water, well water, and lake water with the removal efficiency of > 95%.
从水溶液中去除重金属离子的范围很大。本研究制备了以(3-巯基丙基)三甲氧基硅烷为官能团的介孔二氧化硅材料(mmsm),并将其用于吸附水溶液中的Pb(II)离子。采用一锅水热法将3-巯基丙基三甲氧基硅烷固定在介孔二氧化硅表面,合成了MPTS/MSMs吸附剂。采用FT-IR、XRD、SEM、TEM、TGA、N2吸附-脱附等温线等技术对吸附剂的结构和性能进行了表征。研究了制备的纳米结构对水溶液中Pb(II)离子的吸附适用性,结果表明纳米结构对Pb(II)离子的吸附选择性较好。系统考察了溶液pH、浓度、吸附剂用量、离子干扰效应、接触时间等参数对吸附剂去除效果的影响。当pH = 6时,吸附效率最高(~ 97%),最佳接触时间为30 min,吸附量为50 mg L−1。该吸附剂成功地用于自来水、井水和湖水三种实际水样中的Pb (II)离子的去除,去除率达95%以上。
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引用次数: 0
CuMoO4/ ZnO Nanocomposites: Novel Synthesis, Characterization, and Photocatalytic Performance CuMoO4/ ZnO纳米复合材料:新型合成、表征及光催化性能
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.009
Rahmad Syah, Amjad Hussein Altajer, O. Rasheed, F. Tanjung, Aseel M. Aljeboree, N. A. Alrazzak, A. Alkaim
There are several sources of water contamination. One of the most important pollutant of water is azo dyes-based waste which produced by textile, paper and dye industrials. At this work, the morphological engineered CuMoO4/ ZnO Nanocomposites are prepared via simple and fast hydrothermal-microwave method and applied it as a photocaalyst for degradation of water pollutants. Prepared products is characterized with X-ray diffraction (XRD) analysis, Fourier-transform infrared spectroscopy (FT-IR), Scanning Electron Microscopy (SEM), Ultra violet-Visible (UV-Vis) spectroscopy. The results confirms that size and shape of prepared products is homogenous wih narrow size distribution. In the next step, prepared ZnO, CuMoO4, and ZnO/CuMoO4 nanocomposites were used as catalyst for photodegradation of methylene blue and Rhodamine B. Results showed that ZnO/CuMoO4 nanocomposites have excellent photocatalytic performance. Results indicated that prepared ZnO/CuMoO4 nanocomposites can be degraded 92 and 84% of methylene blue and Rhodamine B under UV irradiation after 70 minutes. The charge transfer from CuMoO4 to ZnO is confirmed by the optical characteristics of ZnO/CuMoO4 nanocomposites. As a result, the potential of electron-hole recombination in CuMoO4 decreases, resulting in holes in the valance band that combine with OH groups on the surface of nanocomposites to form highly reactive OH• radicals. The radicals are damaged when they come into contact with Rhodamine B and Methylene blue.
水污染有几种来源。纺织、造纸和染料工业产生的偶氮染料废水是水污染的主要污染物之一。本文采用简单、快速的水热微波法制备了形态工程CuMoO4/ ZnO纳米复合材料,并将其作为光催化剂用于水污染物的降解。用x射线衍射(XRD)分析、傅里叶变换红外光谱(FT-IR)、扫描电子显微镜(SEM)、紫外可见(UV-Vis)光谱对制备的产物进行了表征。结果表明,制备的产物尺寸和形状均匀,粒径分布窄。下一步,将制备好的ZnO、CuMoO4和ZnO/CuMoO4纳米复合材料作为光降解亚甲基蓝和罗丹明b的催化剂。结果表明,ZnO/CuMoO4纳米复合材料具有优异的光催化性能。结果表明,制备的ZnO/CuMoO4纳米复合材料在紫外线照射70 min后可降解92%和84%的亚甲基蓝和罗丹明B。ZnO/CuMoO4纳米复合材料的光学特性证实了CuMoO4向ZnO的电荷转移。结果,CuMoO4中电子-空穴复合电位降低,导致价带中的空穴与纳米复合材料表面的OH基团结合形成高活性的OH•自由基。当自由基与罗丹明B和亚甲基蓝接触时,它们就会被破坏。
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引用次数: 1
Synthesis and Structural Properties of Eu3+:TiO2 Nanoparticles Eu3+:TiO2纳米颗粒的合成及结构性能
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.015
B. A. Jabar, H. M. Yaseen, M. A. Hamzah, K. J. Tahir, N. Ridha, F. Alosfur, Rajaa A. Madlol, Basheer M. Hussein
Pure and doped TiO2 with Eu3+ nanoparticles were prepared by a novel and simple preparation method. The pure TiO2 nanoparticles and the doping TiO2 with the Eu3+ ions prepared at room temperature by the sol-gel method via the reaction of Titanium (IV) isopropoxide (TTIP) with an aqueous solution of hydrochloric acidic in the presence of ethanol. The crystal structure of the prepared nanoparticles was investigated by X-Ray Diffraction (XRD) while the morphology of the samples was investigated by Field Emission Scanning Electron Microscopy (FESEM). All the prepared samples having excellent crystalline. As well, XRD proved that doping TiO2 with Eu3+ reduced the crystallite size. The FESEM images showed that the doping of TiO2 with Eu3+ results in larger particle sizes. In the present work, the effects of doping, particle size, and stabilization of the anatase phase were studied. As well as the deceleration of crystal growth by the rare-earth-doped into TiO2 host was investigated.
采用一种新颖、简单的制备方法制备了Eu3+纳米颗粒的纯TiO2和掺杂TiO2。以异丙酸钛(TTIP)与乙醇存在的盐酸水溶液为原料,采用溶胶-凝胶法制备了纯TiO2纳米粒子和掺杂Eu3+离子的TiO2。采用x射线衍射(XRD)和场发射扫描电镜(FESEM)研究了制备的纳米颗粒的晶体结构。所制备的样品均具有优异的结晶性。XRD也证明了Eu3+掺杂TiO2可以减小晶粒尺寸。FESEM结果表明,Eu3+掺杂后TiO2颗粒尺寸增大。在本工作中,研究了掺杂、粒度和锐钛矿相稳定性的影响。同时研究了稀土掺杂TiO2载体对晶体生长的抑制作用。
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引用次数: 0
Synthesis of NiO Nanoparticles and Sulfur, and Nitrogen co Doped-Graphene Quantum Dots/ NiO Nanocomposites for Antibacterial Application 纳米NiO与硫、氮掺杂-石墨烯量子点/ NiO纳米复合材料的合成及其抗菌应用
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.019
S. G. Al-Shawi, N. Alekhina, S. Aravindhan, L. Thangavelu, Akulina Elena, N. V. Kartamysheva, R. Zakieva
The human life is faced with bacterial infections which are one of the major cause of prevalence and mortality. Antibiotics have long been the preferred therapy for bacterial infections due to their cost-effectiveness and efficacy. In the field of overcoming microbial issues, new and emerging nanostructure-based materials have gotten a lot of attention. In this Study, NiO and sulfur, and nitrogen co doped-graphene quantum dots-decorated NiO nanocomposites (S,N-GQDs/NiO) are prepared via a simple hydrothermal method. Structural and morphological properties of products are determined via XRD, SEM, UV-Vis, and FTIR analysis. The prepared products are applied for the investigation of antibacterial activity against Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, and methicillin resistant Staphylococcus aureus (MRSA). The results showed that prepared S,N-GQDs/NiO nanocomposites have high antibacterial activity against Staphylococcus aureus among a wide range of microorganisms. For S,N-GQDs/NiO nanocomposites nanoparticles, the disk diffusion test proved that the highest growth inhibition zone was related to Staphylococcus aureus (17 mm). The presence of graphene quantum dots in S,N-GQDs/NiO nanocomposites facilitates reactive oxygen species (ROS) mechanism which lead to bet antibacterial activity.
人类生活面临着细菌感染,细菌感染是导致流行和死亡的主要原因之一。由于其成本效益和疗效,抗生素长期以来一直是细菌感染的首选治疗方法。在克服微生物问题的领域,新兴的基于纳米结构的材料受到了广泛的关注。本研究通过简单的水热法制备了NiO和硫、氮共掺杂-石墨烯量子点修饰的NiO纳米复合材料(S,N-GQDs/NiO)。通过x射线衍射(XRD)、扫描电镜(SEM)、紫外-可见光谱(UV-Vis)和红外光谱(FTIR)分析,确定了产物的结构和形态特征。将制备的产品用于铜绿假单胞菌、大肠杆菌、金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌(MRSA)的抑菌活性研究。结果表明,制备的S,N-GQDs/NiO纳米复合材料对多种微生物中的金黄色葡萄球菌具有较高的抗菌活性。对于S,N-GQDs/NiO纳米复合纳米颗粒,圆盘扩散试验证明,生长抑制区最高的是金黄色葡萄球菌(17 mm)。石墨烯量子点在S,N-GQDs/NiO纳米复合材料中的存在促进了活性氧(ROS)机制,从而提高了抗菌活性。
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引用次数: 53
Rutin: a Flavonoid Precursor for Synthesis of ZnFe2O4 Nanoparticles; Electrochemical Study of Zinc Ferrite-chitosan Nanogel for Doxorubicin Delivery 合成纳米ZnFe2O4的类黄酮前体芦丁铁酸锌-壳聚糖纳米凝胶递送阿霉素的电化学研究
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.013
Mostafa Shafiee, S. H. Ghoran, S. Bordbar, M. Gholami, M. Naderian, Fatemeh Dehghani, A. Amani
The use of core-shell nanoparticles as controlled drug delivery vehicles has proven successful, yet their production and application require costly and toxic chemicals. We hereby use a natural glycosylated flavonoid (rutin) for synthesis of a nanocarrier for doxorubicin delivery. For this target, a convenient two-step synthesis was processed including a synthesis of bio-zinc ferrite nanoparticles without N2 gas and chitosan coating (CS; bio-zincferrite@chitosan). The as-synthesized magnetic nanogel was characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transformed infrared (FT-IR) spectroscopy, and electro-analytical methods including cyclic voltammetry and electrochemical impedance spectroscopies. The collapse/swell potential of the coated CS layers of the bio-NPs were found to be responsible for the observed pH dependence of doxorubicin delivery. Results exhibited the drug release of bio-nanogel can be induced at pH ranging from 6 to 7. Therefore, capacity and efficiency parameters of the anti-cancer drug onto the NPs were obtained as equal to 43.5% and 78.6%. The present work provides a simple method to fabricate smart pH-responsive nanogel for cancer therapy.
核壳纳米粒子作为受控药物递送载体的使用已被证明是成功的,但它们的生产和应用需要昂贵和有毒的化学品。我们在此使用一种天然糖基化的类黄酮(芦丁)合成了一种用于阿霉素递送的纳米载体。针对这一目标,采用了两步合成方法:无N2气合成生物铁氧体锌纳米颗粒,壳聚糖包覆(CS;bio-zincferrite@chitosan)。利用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、傅里叶变换红外光谱(FT-IR)以及循环伏安法和电化学阻抗谱等电分析方法对合成的磁性纳米凝胶进行了表征。发现生物nps包被的CS层的坍塌/膨胀电位是观察到的阿霉素递送的pH依赖性的原因。结果表明,pH为6 ~ 7时,生物纳米凝胶可诱导药物释放。因此,得到的抗癌药物在NPs上的容量和效率参数分别为43.5%和78.6%。本研究提供了一种制备用于癌症治疗的智能ph响应纳米凝胶的简单方法。
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引用次数: 1
Study of the Physicochemical Properties and Antimicrobial Activities of Nanoparticles Containing β-Cyclodextrin and Geranial 含β-环糊精和香叶醛纳米颗粒的理化性质及抗菌活性研究
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.020
M. Maleki, Z. Hadian, K. Abdi, Paliz Koohy-Kamaly, F. Bahmanyar
In general, β-cyclodextrin (β-CD) is widely used in various technologies of the food industries. The aims of this study were preparation, characterization and optimization of a novel nanosize formulation of β-CD NPs loaded with GR. In the current study optimum conditions for maximum encapsulation efficiency and loading of geraniol using response surface methodology (RSM) was assessed. Furthermore, the in-vitro antimicrobial activities against S. aureus, B. cereus, S. enteritidis, E. coli, C. albicans and A. niger were studied. The present study is the first to investigate the antimicrobial activity of the GR inclusion complexes in nanosize formulations. The GR complexes were evaluated using scanning electron microscopy (SEM), infrared (IR) spectroscopy and differential scanning calorimetry (DSC). Furthermore, antimicrobial activity of the inclusion complexes (IC) against bacteria and fungi were assessed. Minimum inhibitory concentrations (MIC) and inhibition zones of the GR-β-CD inclusion complexes were calculated using agar/broth dilution and agar well-diffusion methods. The EE and loading values of the optimized formulation included 87.25 and 10.45%, respectively, with a size distribution of 117 nm ±1 and appropriate particle size distribution (PDI). Moreover, SEM, IR and DSC verified fabrication of inclusion complexes between GR and β-CD. The inhibition zones of β-CD-GR complexes were recorded as the following order: Bacillus cereus > Staphylococcus aureus > Salmonella entritidis > Escherichia coli. The RSM technique allowed to prepare geraniol nanoinclusion complexes using β-cyclodextrin with optimum responses. The antimicrobial activity of GR highly enhanced after efficient complexation. This study generates appropriate information for application of inclusion complexes of GR.
总的来说,β-环糊精(β-CD)广泛应用于食品工业的各种技术中。本研究的目的是制备、表征和优化一种新型的纳米级载GR β-CD NPs配方。本研究利用响应面法(RSM)评价了香叶醇包封和载药的最佳条件。此外,还研究了其对金黄色葡萄球菌、蜡样芽孢杆菌、肠炎葡萄球菌、大肠杆菌、白色念珠菌和黑曲霉的体外抑菌活性。本研究首次研究了纳米级配方中GR包合物的抗菌活性。采用扫描电镜(SEM)、红外光谱(IR)和差示扫描量热法(DSC)对GR配合物进行了评价。此外,还研究了包合物对细菌和真菌的抑菌活性。采用琼脂/肉汤稀释法和琼脂孔扩散法计算GR-β-CD包合物的最小抑制浓度(MIC)和抑制区。优化后的配方EE和负载值分别为87.25和10.45%,粒径分布为117 nm±1,粒径分布(PDI)适宜。此外,SEM、IR和DSC验证了GR与β-CD之间包合物的制备。β-CD-GR复合物的抑菌区顺序为:蜡样芽孢杆菌>金黄色葡萄球菌>肠炎沙门氏菌>大肠杆菌。采用RSM技术制备香叶醇纳米包合物,反应最佳。GR经高效络合后,抗菌活性显著增强。本研究为GR包合物的应用提供了适当的信息。
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引用次数: 0
Sonochemical Preparation of Magnesium Hydroxide and Aluminum Hydroxide Nanoparticles for Flame Retardancy and Thermal Stability of Cellulose Acetate and Wood 声化学法制备用于醋酸纤维素和木材阻燃和热稳定性的氢氧化镁和氢氧化铝纳米颗粒
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.004
Mahya Tamiji, Ali Reza Ahmadian-Fard-Fini, Manouchehr Behzadi, D. Ghanbari
In this work firstly magnesium hydroxide (Mg(OH)2) and aluminum hydroxide (Al(OH)3) were prepared using sono-chemical reaction at solvent of water without applying any surface active agent. Effect of various sono-chemistry parameters such as power, cycles, time and volume on the size and shape of nanostructures were investigated. Secondly nanoparticles were modified and coated by ethyl cellulose capping agent. Modified nanoparticles were added to cellulose acetate and surface of wood for investigation of flame retardancy. Thermal stability were characterized by thermal gravimetric analysis (TGA). Flame retardancy were examined by UL-94 and heat release tests.
本文首先在不添加任何表面活性剂的情况下,在水的溶剂下采用声化学反应法制备了氢氧化镁(Mg(OH)2)和氢氧化铝(Al(OH)3)。研究了功率、循环次数、时间和体积等不同声化学参数对纳米结构尺寸和形状的影响。其次,采用乙基纤维素封盖剂对纳米颗粒进行修饰和包被。将改性纳米颗粒添加到醋酸纤维素和木材表面,研究其阻燃性。热重分析(TGA)表征了材料的热稳定性。通过UL-94和放热试验检测了阻燃性。
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引用次数: 1
Synthesis of CdSe and CdTe Quantum Dots: Their Effects on the Znq2 Luminescence Complex for Organic Light Emitting Diodes CdSe和CdTe量子点的合成及其对有机发光二极管Znq2发光配合物的影响
IF 1.4 Q3 Engineering Pub Date : 2021-01-01 DOI: 10.22052/JNS.2021.01.017
M. Jafari, Zeynab Sadat Alirahmi, D. Ghanbari
CdSe and CdTe quantum dots were synthesized by a simple hydrothermal method using ammonia and hydrazine in a short time period of 5 hours. In another phase, Znq2 complex nanostructures were prepared using a green environmentally friendly method, in which saffron extract was used as surfactant. The purity of the nanoparticles was investigated by X-ray diffraction and their dimensions and morphology were studied by scanning electron microscopy. In the next step, CdSe and Znq2 complexes were synthesized and their synergistic effects on each other was investigated. The photoluminescence results show the luminescence of all three nanostructures in the visible light range, and it was concluded that upon compositing these nanostructures, their luminescence properties remained intact. Their optical and structural properties were investigated using X-ray diffraction (XRD) analysis, infrared spectroscopy (FT-IR), ultraviolet and visible light (UV-Visible) spectroscopy, photoluminescence spectroscopy (PL) and electron imaging (SEM).Key Words: Synthesis of Quantum Dots, Znq2 Complex, Organic Light Emitting Diode
采用简单的水热法,以氨和肼为原料,在5小时内合成了CdSe和CdTe量子点。另一相以藏红花提取物为表面活性剂,采用绿色环保的方法制备了Znq2复合纳米结构。用x射线衍射研究了纳米颗粒的纯度,用扫描电镜研究了纳米颗粒的尺寸和形貌。下一步,我们合成了CdSe和Znq2配合物,并研究了它们之间的协同作用。光致发光结果表明,这三种纳米结构都在可见光范围内发光,表明复合后的纳米结构的发光性能保持不变。利用x射线衍射(XRD)分析、红外光谱(FT-IR)、紫外和可见光(UV-Visible)光谱、光致发光光谱(PL)和电子成像(SEM)研究了它们的光学和结构性质。关键词:量子点合成,Znq2配合物,有机发光二极管
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Journal of Nanostructures
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