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1.
在制备超细Fe3O4磁性粒子的基础上, 利用可控制自由基聚合DPE法制备出平均粒径为265 nm的P(AA-MMA-ST)/Fe3O4磁性复合微球. 采用XRD, TGA, FTIR等手段对所制备的磁性复合微球的形态、结构及磁响应性等进行了表征, 结果表明用DPE法制备出的磁性复合微球磁含量较高, 粒径比较均匀.  相似文献   

2.
可控制自由基聚合DPE法制备P(AA-MMA-ST)/Fe3O4磁性复合微球   总被引:2,自引:0,他引:2  
在制备超细Fe3O4磁性粒子的基础上, 利用可控制自由基聚合DPE法制备出平均粒径为265 nm的P(AA-MMA-ST)/Fe3O4磁性复合微球. 采用XRD, TGA, FTIR等手段对所制备的磁性复合微球的形态、结构及磁响应性等进行了表征, 结果表明用DPE法制备出的磁性复合微球磁含量较高, 粒径比较均匀.  相似文献   

3.
 采用种子乳液聚合方法制得了微米尺度的高磁性物质含量的磁性复合微球.聚合体系中,以0.7~0.8 μm的Fe3O4磁性聚集体细乳液作为种子,将苯乙烯,二乙烯基苯作为聚合单体加入到磁性聚集体细乳液中,对Fe3O4磁性聚集体进行溶胀后进行聚合.研究了聚合过程中,溶胀时间对复合微球形貌和磁性物质含量的影响,获得系列形貌微球.通过透射电镜(TEM)、热重分析(TGA)、红外分析(FTIR)、振动样品磁强计(VSM)等表征手段对所制备的磁性聚合物微球进行分析表征.结果显示,所得到的磁性聚合物微球粒度为0.7~1 μm,尺寸分布较均一,具有超顺磁性,磁性物质含量为29 wt%~57 wt%.然后又通过丙烯酸和苯乙烯共聚对微球表面羧基功能化后,得到了表面羧基密度为0.92 mmol/g的微球,再将所制备的微球与生物分子偶联后(以hCG作为模式待检分子),在化学发光免疫检测上进行了初步的应用,取得到了较好的应用结果.  相似文献   

4.
磁性多孔γ-Fe_2O_3/P(St-DVB-MAA)聚合物微球的制备及其表征   总被引:1,自引:0,他引:1  
以油酸包裹的γ-Fe2O3为磁性来源,选用苯乙烯(St)、二乙烯苯(DVB)和甲基丙烯酸(MAA)为共聚单体,通过改进的悬浮聚合法,制备了表面含有羧基的多孔磁性高分子微球.利用红外光谱(FTIR)、扫描电子显微镜(SEM)、光学显微镜以及热重分析仪(TG)等对聚合物进行了性能表征.FTIR和光学显微镜结果分析表明,苯乙烯、二乙烯苯和甲基丙烯酸在磁性粒子的表面发生了聚合反应,生成了聚合物包埋磁粉的磁性聚合物复合微球,且微球表面含有羧基;SEM和光学显微镜分析测试结果显示合成的磁性γ-Fe2O3/P(St-DVB-MAA)复合粒子呈球形,微球具有多孔结构,且微球之间不发生团聚,微球粒子粒径分布均匀,大多数粒子粒径分布在0.4~0.9mm之间;TG测试的结果表明,磁性γ-Fe2O3被包覆在聚合物微球之中,且磁性粒子在微球中的包覆率达到12.12%.  相似文献   

5.
以球磨后的粉煤灰磁珠(MS)颗粒为磁核,通过溶胶凝胶法和反相微乳液法依次包覆SiO2和壳聚糖(CS),制备了MS@SiO2@CS磁性微球。利用扫描电镜及能量色散谱仪、热重分析仪、红外光谱仪、X射线衍射仪、振动样品磁强计对所得样品的结构和磁性进行了系统表征。结果表明,磁珠颗粒表面实现了逐层包覆,较均匀的分散于壳聚糖基体中,MS@SiO2@CS微球的比饱和磁化强度可达7.04 emu·g-1。Cu2+离子吸附实验表明,所得磁性壳聚糖微球对Cu2+具有良好的吸附能力,最大吸附量可达11.08 mg·g-1;而且可通过磁选法高效固液分离。吸附动力学研究表明,MS@SiO2@CS微球对Cu2+离子的吸附符合准二级动力学模型,以化学吸附为主。  相似文献   

6.
表面图案化磁性复合微球的原位制备与表征   总被引:2,自引:0,他引:2  
王公正  夏慧芸  张颖  彭世杰 《化学学报》2007,65(18):2051-2056
采用反相悬浮聚合法合成了丙烯酸(AA)含量不同的N-异丙基丙烯酰胺-丙烯酸共聚物P(NIPAM-co-AA)微凝胶, 并以其作为微反应器, 通过原位外源沉积法制备了一系列微米级、表面具有图案化结构的SiO2-Fe3O4-P(NIPAM-co-AA)磁性复合微球. 实验结果表明, 复合微球的表面结构与微凝胶的组成、Fe3O4和SiO2的沉积量有关. 在微球表面进行修饰, 可得到表面带有氨基等官能基团的磁性复合材料. 将这种功能化磁性微球用于识别生物大分子并进一步用于生物医学领域具有重要的意义.  相似文献   

7.
以共沉淀法制备出Fe3O4纳米粒子,通过聚乙烯亚胺(PEI)修饰Fe3O4纳米粒子,再原位复合上Au纳米粒子,制得Fe3O4/PEI/Au纳米颗粒微球。再将Fe3O4/PEI/Au纳米颗粒与巯基乙酸修饰的量子点CdSe/CdS连接,成功制备了Fe3O4/PEI/Au@CdSe/CdS多功能复合微球。经过傅里叶变换红外光谱仪(FTIR)、荧光分光光度计、荧光显微镜、X射线衍射(XRD)、透射电子显微镜(TEM)及振动样品磁强计(VSM)的表征。结果表明:多功能复合微球的粒径在40nm左右,具有超顺磁性,剩磁,矫顽力近似等于零,饱和磁化强度为28.83A·m2·kg-1,同时兼有优越的荧光性能和金纳米粒子的特性。  相似文献   

8.
以共沉淀法制备出Fe3O4纳米粒子,通过聚乙烯亚胺(PEI)修饰Fe3O4纳米粒子,再原位复合上Au纳米粒子,制得Fe3O4/PEI/Au纳米颗粒微球。再将Fe3O4/PEI/Au纳米颗粒与巯基乙酸修饰的量子点CdSe/CdS连接,成功制备了Fe3O4/PEI/Au@CdSe/CdS多功能复合微球。经过傅里叶变换红外光谱仪(FTIR)、荧光分光光度计、荧光显微镜、X射线衍射(XRD)、透射电子显微镜(TEM)及振动样品磁强计(VSM)的表征。结果表明:多功能复合微球的粒径在40 nm左右,具有超顺磁性,剩磁,矫顽力近似等于零,饱和磁化强度为28.83 A·m2·kg-1,同时兼有优越的荧光性能和金纳米粒子的特性。  相似文献   

9.
徐烽  李良超  蒋静  谢云龙 《化学学报》2007,65(9):816-820
用柠檬酸盐前驱物-溶胶凝胶法制备了Zn0.4Ni0.6Cr0.5LaxFe1.5-xO4 (x=0~0.10)纳米粉晶. 用DSC-TG分析了前驱物转变为粉晶的热分解过程, 通过粉末X射线衍射仪(XRD)、透射电子显微镜(TEM)和振动样品磁强计(VSM)等表征了产物的结构、形貌和磁性能. 结果表明, 不同温度和不同的La掺杂量对样品的晶粒尺寸、晶胞参数和形貌均产生了明显的影响, 且通过改变La含量能起到调控样品磁性能的作用.  相似文献   

10.
免疫磁性纳米微球的制备与表征   总被引:1,自引:0,他引:1  
王斌 《化学通报》2015,78(9):847-850
成功制备了Fe3O4磁性纳米颗粒及二甲基丙烯酸乙二醇酯-甲基丙烯酸(EGDMA-MAA)共聚物包覆的Fe3O4磁性复合微球。将吲哚美辛抗体固定在复合微球表面,形成了Fe3O4(核)/聚合物-抗体(壳)的复合免疫磁性颗粒。XRD结果表明,制备的Fe3O4的晶型为反立方尖晶石型且纯度较高;TEM表征表明Fe3O4粒径较为均匀,平均粒径为12nm;磁性复合微球的平均直径为460nm。制备的Fe3O4磁性纳米颗粒和磁性复合微球有较强的磁响应强度,其饱和磁化率分别为49.16和8.38emu/g,能够满足磁性分离的要求。FT IR验证了磁性复合微球中羧基特征峰的存在,表明羧基成功连接在磁性微球上面。通过碳二亚胺/N-羟基琥珀酰亚胺(EDC/NHS)活化法将微球表面羧基活化并成功与抗吲哚美辛抗体交联。  相似文献   

11.
有机磁合成化学研究进展   总被引:11,自引:0,他引:11  
陆模文  胡文祥 《有机化学》1997,17(4):289-294
通过磁场对聚合反应、酯化反应、光还原反应和不对称合成等的影响,论述了有机磁化学的理论研究和应用进展。磁场在一定程度上影响有机反应的反应速率、产率、反应途径和产物构成。同时初步探讨了磁场影响化学反应速率的机理,并展望了磁化学的发展前景。  相似文献   

12.
Magnetic nano- and microparticles in biotechnology   总被引:1,自引:0,他引:1  
Both synthetic and biologically produced magnetic nano- and microparticles exhibit several types of responses to external magnetic field which have been already employed in various areas of biosciences, biotechnology, medicine, environmental technology, etc. This short review shows selected important biotechnological applications of magnetic particles, and the biological processes leading to biogenic magnetic particles formation. Presented at the 1st Nanomaterials and Nanotechnology Meeting, Nano Ostrava, Ostrava, Czech Republic, 1–4 September 2008.  相似文献   

13.
Cu(hfac)2 chain polymer heterospin complexes with pyrazole-substituted nitronylnitroxides (LR, where R = Me, Et) with a composition Cu(hfac)2LR, exhibiting structural rearrangements with magnetic effects in the solid state at reduced temperatures, were studied by magnetic resonance. The magnetic resonance spectrum changes substantially for substituents of different types. The results of this study are discussed in the context of the cluster approach in view of the specific crystal structure of the compounds.  相似文献   

14.
In the diamond industry, ferrofluids are used in ferrohydrostatic separators for the density separation of diamonds from gangue material. The size of the magnetic core of the coated particles forming the ferrofluid suspension is vital in ensuring the stability of the fluid. The particle size must be small enough such that sedimentation does not occur in a magnetic field gradient and under the influence of a gravitational field and such that magnetic agglomeration can be overcome. This paper discusses the particle size requirements for fluid stability under the influence of these effects.  相似文献   

15.
Anisotropy counts: A brief review of the main physical properties of elongated magnetic particles (EMPs) is presented. The most important characteristic of an EMP is the additional contribution of shape anisotropy to the total anisotropy energy of the particle, when compared to spherical magnetic particles. The electron micrograph shows Ni‐ferrite microrods fabricated by the authors.

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16.
Magnetic nanoadsorbents using Fe3O4 nanoparticles as cores and poly(methyl acrylic acid) (PMAA) as ionic exchange groups were prepared through our novel approach. Two steps were involved in this approach: the first was to functionalize the magnetic nanoparticles (MNPs) with methacrylate double bonds via the combination of ligand exchange and condensation of methacryloxypropyltrimethoxysilane(MPS); the second was to graft PMAA chains onto the surface of MNPs through radical polymerization. The success of the various surface functionalization steps was ascertained using FTIR and XPS. The as‐synthesized PMAA‐coated MNPs were effective in binding bovine serum albumin (BSA) with a high capacity of 1 300 mg · g−1.

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17.
双层表面活性剂分散制备水基磁流体   总被引:20,自引:0,他引:20  
Fe3O4 magnetic particles were synthesize by chemical co-precipitation. Sodium oleate and poly(ethylene glycol)-4000 were used as bilayer surfactants to envelope the ultra-fine Fe3O4 particles. Then stabilized water base magnetic fluid was obtained. Experiments indicated that surfactants and pH value of the solution had great effect on the stability and size of the magnetic fluid when Fe3O4 particles were synthesized and enveloped. It was the first time to employ this method to prepare magnetic fluid. Using laser diffraction particle size analyzer we found that the average diameter of magnetic fluid was lessen than 84 nanometer. Its magnetization was measured on magnetic balance and the result amounted to 3.84×103A·m-1. Further more, XRD and IR analysis measurements were employed to substantiate the existence of Fe3O4 and surfactant structure. The magnetic fluid can be used as tar-geted-part of nanometer targeted drug delivery system.  相似文献   

18.
This study aims to develop an effective method to control motile microorganisms and enable their manipulation as functional ‘live micro/nano robots'. A novel strategy based on Fe3O4 nanoparticle‐doped alginate hydrogel is developed to fashion an artificial extracellular matrix (ECM) for microbial cells (e.g., Saccharomyces cerevisiae and Flavobacterium heparinum). During this strategy, a single layer of alginate hydrogel is coated around the microbial cells doped with Fe3O4 nanoparticles to form the alg‐mag‐cells. Transmission electron microscopy shows that Fe3O4 nanoparticles are uniformly distributed in the hydrogel shell. Together with maintaining the cell activity and metabolism, the hydrogel coated microbial cells demonstrate high magnetic responsiveness in an external magnetic field and are able to form micro‐scaled patterns using the magnetic template designed in this study. This strategy provides a building block to fabricate advanced biological models, medical therapeutic products, and non‐medical biological systems using different microorganisms.

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19.
Polarized neutron diffraction (PND) experiments were carried out at low temperature to characterize with high precision the local magnetic anisotropy in two paramagnetic high‐spin cobalt(II) complexes, namely [CoII(dmf)6](BPh4)2 ( 1 ) and [CoII2(sym‐hmp)2](BPh4)2 ( 2 ), in which dmf=N,N‐dimethylformamide; sym‐hmp=2,6‐bis[(2‐hydroxyethyl)methylaminomethyl]‐4‐methylphenolate, and BPh4?=tetraphenylborate. This allowed a unique and direct determination of the local magnetic susceptibility tensor on each individual CoII site. In compound 1 , this approach reveals the correlation between the single‐ion easy magnetization direction and a trigonal elongation axis of the CoII coordination octahedron. In exchange‐coupled dimer 2 , the determination of the individual CoII magnetic susceptibility tensors provides a clear outlook of how the local magnetic properties on both CoII sites deviate from the single‐ion behavior because of antiferromagnetic exchange coupling.  相似文献   

20.
Bimetallic ferrimagnet [Cr(CN)6][Mn(R)-pnH(H2O)]H2O with crystallographical chirality of space group P212121 exhibits a giant third-order harmonic susceptibility at around 38 K. This anomaly appears as precursory magnetic phenomenon of the magnetic ordering. In order to investigate the effect of lattice distortion on this giant nonlinear magnetic response (NLMR) and finally elucidate the correlation between the structural chirality and the giant NLMR, we performed the ac susceptibility measurement for the single crystal in the situation of bringing about lattice distortion along the direction parallel to the a-axis. This giant NLMR was drastically suppressed even by slight strain, whereas the traces could be confirmed in the region up to 3.7 kbar. We conclude that the appearance of the giant NLMR requires crystal chirality well-regulated over the crystal.  相似文献   

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