WO2023221298A1 - 一种西兰花状微纳米银的制备方法及其应用 - Google Patents

一种西兰花状微纳米银的制备方法及其应用 Download PDF

Info

Publication number
WO2023221298A1
WO2023221298A1 PCT/CN2022/109869 CN2022109869W WO2023221298A1 WO 2023221298 A1 WO2023221298 A1 WO 2023221298A1 CN 2022109869 W CN2022109869 W CN 2022109869W WO 2023221298 A1 WO2023221298 A1 WO 2023221298A1
Authority
WO
WIPO (PCT)
Prior art keywords
broccoli
silver
nano silver
micro
concentration
Prior art date
Application number
PCT/CN2022/109869
Other languages
English (en)
French (fr)
Inventor
邢铁玲
邢丽丽
陈国强
Original Assignee
苏州大学
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 苏州大学 filed Critical 苏州大学
Publication of WO2023221298A1 publication Critical patent/WO2023221298A1/zh

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00—Making metallic powder or suspensions thereof
    • B22F9/16—Making metallic powder or suspensions thereof using chemical processes
    • B22F9/18—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
    • B22F9/24—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/05—Metallic powder characterised by the size or surface area of the particles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B22—CASTING; POWDER METALLURGY
    • B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/06—Metallic powder characterised by the shape of the particles
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/65—Raman scattering
    • G01N21/658—Raman scattering enhancement Raman, e.g. surface plasmons
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00—Technologies for wastewater treatment
    • Y02W10/30—Wastewater or sewage treatment systems using renewable energies
    • Y02W10/37—Wastewater or sewage treatment systems using renewable energies using solar energy

Definitions

  • the invention belongs to the field of new materials and surface-enhanced Raman light detection, and relates to a preparation method of broccoli-shaped micro-nano silver and its application.
  • Metal nanostructures have richer and more stable chemical and physical properties, so the preparation of nanoscale metal structures will become a major research hotspot in the field of nanomaterials.
  • Flower-shaped micro-nano silver is a kind of precious metal nanomaterial. Due to its unique size and morphology, it shows excellent properties in antibacterial properties, conductivity, optics, etc., and can be widely used in chemical catalysis, surface-enhanced drawing, etc. Man and optoelectronic devices and other fields.
  • Caffeic acid is one of the natural polyphenols. It has good anti-inflammatory, antibacterial, antiviral and other pharmacological effects. It is also a good green reducing agent.
  • Surface-enhanced Raman scattering spectroscopy is a fast, non-destructive material structure analysis method, and has practical and extensive applications in biological monitoring, environmental monitoring, food safety testing and other fields.
  • most surface-enhanced Raman substrates are based on noble metal nanostructures or nano-rough surfaces to enhance the local electromagnetic field intensity and thereby amplify the Raman scattering signals of the sample molecules to be measured around the noble metal nanostructures.
  • Preparation methods of noble metal nanostructures include physical etching, chemical synthesis, light induction, electrochemical and biological methods.
  • the metal nanostructures synthesized by the chemical reduction method are diversified, have few defects, and are relatively simple to operate. They are ideal for preparing nanostructures.
  • One of the common methods of structure However, most current chemical methods require the introduction of a large number of chemical reagents, resulting in problems such as high production costs and environmental pollution.
  • the purpose of the present invention is to solve the problems existing in the prior art and provide a preparation method and application of broccoli-shaped micro-nano silver.
  • a method for preparing broccoli-like micro-nano silver A phenolic acid compound aqueous solution with a concentration of 2-3mg/mL and a silver ammonia solution with a concentration of 0.8-1.2mol/L are respectively prepared. After dropping the silver ammonia solution, stir for 15-20 minutes, and then conduct an ultrasonic reaction at 25-30°C at an ultrasonic frequency of 80-100KHz for 60-90 minutes to obtain broccoli-like micro-nano silver, in which the phenolic acid compound The volume ratio of the aqueous solution to the silver ammonia solution is 67:1; after the reaction is completed, the broccoli-like micro-nano silver needs to be centrifuged, washed with ethanol and deionized water, and the centrifugation and washing steps are repeated 3-4 times;
  • the molecule In the phenolic structure of phenolic acid compounds, due to the presence of double bonds on the benzene ring and the side chain of the benzene ring, the molecule has a large conjugated system, and due to the presence of carboxyl groups, the conjugated system has a greater electron-attracting ability.
  • the oxygen atom In the phenolic hydroxyl COH structure, the oxygen atom contains a lone pair of p electrons. The p electron cloud and the large ⁇ electron cloud in the conjugated system overlap from the side.
  • the p electron cloud on the oxygen atom Transfer to the benzene ring, the electron cloud between hydrogen and oxygen atoms transfers to the direction of the oxygen atom, and the OH bond on the phenolic hydroxyl group tends to break, generating an o-phthaloquinone structure.
  • the OH bond on the phenolic hydroxyl group of small molecule phenolic acid compounds is The dissociation energy (BED) is usually around 200-400kJ/mol.
  • the reaction solution is ultrasonically treated with an ultrasonic frequency of 80-100KHz with sufficient intensity, and an "acoustic cavitation" effect occurs in the solution, instantly releasing high temperatures above 5000K, high pressures above 5.05 ⁇ 10 8 Pa, and speeds above 110m/ s of strong impact microjet, these energies (as long as the ultrasonic frequency is 80-100KHz to ensure the generation of these energies) can open chemical bonds with a bond energy of about 370-420KJ/mol, which is enough to break the OH bond in the phenolic hydroxyl group and promote hydrogen Atoms leave and the quinoid structure forms.
  • the carboxyl anions in the small molecule phenolic acid compounds capture the positively charged Ag + from the solution through electrostatic complexation, forming a relatively stable complex that originally moved freely between the conjugated ring and the side chain double bond.
  • the electrons are gradually attracted to Ag + under the influence of electrostatic force.
  • Ag + captures the electrons, which are reduced to silver atoms and released.
  • Silver atoms in the solution continue to aggregate into silver crystal nuclei (a small part of the silver crystal nuclei is formed before ultrasound, and most of the silver crystal nuclei are formed after ultrasound. Because the mixture is stirred for 15-20 minutes before ultrasound, there will be silver in this process. The atoms are reduced and then silver crystal nuclei are formed.
  • this process is relatively mild, the reduction rate is slow, and the number of silver crystal nuclei formed in a short time is small. More silver atoms will be absorbed by the subsequent ultrasonic process. It is continuously reduced to form silver crystal nuclei.
  • the stirring process before the ultrasonic reaction is mainly to ensure that the reducing agent and the silver source can be mixed evenly and fully contacted.
  • this process is also accompanied by the reduction of the silver source to form crystal nuclei.
  • the energy of the system increases, and the two-dimensional petal-like silver structure in the solution gains more kinetic energy, moves rapidly and irregularly in the solution, collides with each other, and forms a three-dimensional silver bud structure.
  • the present invention controls the concentration of the phenolic acid compound aqueous solution, the concentration of the silver ammonia solution, the volume ratio of the phenolic acid compound aqueous solution and the silver ammonia solution,
  • the stirring time, ultrasonic temperature, ultrasonic frequency, and ultrasonic reaction time before ultrasonic reaction ensure that the number of three-dimensional silver buds can exceed the critical agglomeration concentration before the end of the ultrasonic reaction), and each three-dimensional silver bud will randomly continue to aggregate with adjacent buds in all directions to form There are nearly flower clusters of silver particles, and the flower-like silver structure is basically formed.
  • the shock waves and micro-jet generated by the acoustic cavitation phenomenon continuously hit the surface of the above-mentioned silver petals, silver flower buds and silver flower clusters.
  • the preparation method of broccoli-shaped micro-nano silver, the phenolic acid compound is caffeic acid, ferulic acid or chlorogenic acid.
  • a method for preparing broccoli-shaped micro-nano silver as described above The preparation process of the silver ammonia solution is: first prepare a silver nitrate solution with a concentration of 0.8-1.2 mol/L, and then drop ammonia water into it to prepare silver. ammonia solution.
  • the stirring speed is 200-300r/min
  • the stirring is to make the reducing agent and the silver source mix evenly and make full contact
  • the stirring speed can be set as long as Just ensure that the above purpose is achieved.
  • a method for preparing broccoli-shaped micro-nano silver as described above the stirring is performed at a temperature of 26 ⁇ 2°C.
  • the invention also provides an application of broccoli-like micro-nano silver.
  • the dispersion of broccoli-like micro-nano silver is added dropwise on a glass slide and then dried to form a SERS for detecting rhodamine 6G, melamine or malachite green.
  • a substrate, wherein broccoli-shaped micro-nano silver is prepared by the preparation method as described in any one of the above.
  • the process of detecting rhodamine 6G, melamine or malachite green is: configure rhodamine 6G, melamine or malachite green into the sample solution to be tested and then drop it in SERS After being applied to the substrate, it was dried and placed under a Raman spectrometer for testing.
  • the concentration of the broccoli-like micro-nano silver dispersion is 2.16-10.8 mg/L, and the concentration of the sample solution to be tested is 10 -4 -10 -10 mol/ L, the volume of the dropped broccoli-like micro-nano silver dispersion is the same as the volume of the dropped sample solution to be tested.
  • the laser wavelength selected for testing was 785nm.
  • Phenolic acid compounds can easily capture positively charged Ag ions from solution and form relatively stable complexes with them. However, due to the reducing nature of phenolic acid compounds, the silver ions trapped in the complex will be reduced to silver atoms by the phenolic acid compounds and released. Silver atoms begin to nucleate slowly and unevenly. As the reaction continues, silver atoms begin to aggregate into primary silver crystals. The number of silver precursors further increases, and more silver atoms are in the process of gradual deposition, forming graded Ag particles with different surface roughness. In addition, ultrasonic treatment can produce acoustic cavitation, thereby accelerating the reaction and promoting the formation of three-dimensional flower-like silver microstructures.
  • the preparation method of the present invention does not introduce other harmful chemical reagents, and is environmentally friendly and energy-saving;
  • the preparation method of the present invention combines chemical reduction methods with physical methods, avoiding the introduction of more chemical reagents, and can reduce production costs and environmental pollution to a certain extent. ;
  • the surface of the broccoli-like micro-nano silver produced by the present invention has a layer-by-layer micro-convex structure, which can provide more SERS hot spots under laser irradiation, has more excellent surface-enhanced Raman signal method capabilities, and can More accurate, sensitive, convenient, real-time and rapid Raman signal detection;
  • Figure 1 is an SEM image of the broccoli-shaped micro-nano silver prepared in Example 1;
  • Figure 2 is an SEM image of the broccoli-shaped micro-nano silver prepared in Example 2;
  • Figure 3 shows the surface-enhanced Raman spectra of rhodamine 6G produced by broccoli-shaped micro-nano silver prepared in Example 1 and purchased spherical silver nanoparticles respectively;
  • Figure 4 shows the surface-enhanced Raman spectra of malachite green produced by broccoli-shaped micro-nano silver prepared in Example 2 and purchased spherical silver nanoparticles;
  • Figure 5 shows the surface-enhanced Raman spectra of melamine of broccoli-like micro-nano silver prepared in Example 3 and purchased spherical silver nanoparticles.
  • the product number of the spherical silver nanoparticles is S196425-25g, which is from Suzhou Great Pharmaceutical Technology Co., Ltd.
  • the specific process is as follows: first prepare a silver nitrate solution with a concentration of 1 mol/L, and then drop ammonia water into it to prepare a silver ammonia solution;
  • the broccoli dropped The volume of the micro-nano silver dispersion is the same as the volume of the dropped sample solution to be tested, which is 30 ⁇ L; the laser wavelength selected for the test is 785nm, the integration time is 10s, the laser power is 5mW, and the laser spot is 1um.
  • the purchased spherical silver nanoparticles were dispersed in an aqueous solution to prepare a nanosilver particle aqueous solution with a concentration of 4.3mg/mL. Then a nanosilver SERS substrate was prepared according to the above method to detect the same concentration of rhodamine 6G. aqueous solution.
  • a method for preparing nanosilver is basically the same as Example 1, except that the ultrasonic frequency is 110 KHz.
  • the shape of the finally prepared nanosilver is a flower shape with a smooth surface and a diameter of 200-400nm.
  • the impact force of the shock wave and micro-jet formed becomes smaller, and the impact on the surface of silver petals, silver flower buds and silver flower clusters becomes weaker, and the surface roughness and unevenness are less obvious and relatively more durable. smooth.
  • a method for preparing nanosilver is basically the same as Example 1, except that the ultrasonic frequency is 70KHz.
  • the shape of the finally prepared nanosilver is irregular spherical with a diameter of 700-800nm.
  • the impact force of the shock wave and micro-jet formed becomes stronger, and the impact on the surface of silver petals, silver flower buds and silver flower clusters becomes stronger. Due to the low frequency Under low frequency, the cavitation bubbles grow for a long time, so the number of mechanical hits on the surface of nanosilver is not as frequent and regular as that of cavitation bubbles on the surface of nanosilver at high frequency, so the surface of nanosilver is uneven at low frequency. It will be obvious and irregular.
  • a method for preparing nanosilver is basically the same as Example 1, except that the reducing agent is sodium borohydride instead of caffeic acid.
  • the shape of the finally prepared nanosilver is an irregular block with a diameter of 800-1000nm.
  • the specific process is as follows: first prepare a silver nitrate solution with a concentration of 1 mol/L, and then drop ammonia water into it to prepare a silver ammonia solution;
  • the broccoli dropped The volume of the micro-nano silver dispersion is the same as the volume of the dropped sample solution to be tested, which is 30 ⁇ L; the laser wavelength selected for the test is 785nm, the integration time is 10s, the laser power is 5mW, and the laser spot is 1um.
  • the purchased spherical silver nanoparticles were dispersed in an aqueous solution to form a silver nanoparticle aqueous solution with a concentration of 6.5 mg/mL, and then a nanosilver SERS substrate was prepared according to the above method to detect the same concentration of malachite green. aqueous solution.
  • the specific process is as follows: first prepare a silver nitrate solution with a concentration of 1 mol/L, and then drop ammonia water into it to prepare a silver ammonia solution;
  • the dropped broccoli-like micro-nano silver The volume of the dispersion is the same as the volume of the dropped sample solution to be tested, both 30 ⁇ L; the laser wavelength selected for the test is 785nm, the integration time is 10s, the laser power is 5mW, and the laser spot is 1um.
  • the purchased spherical silver nanoparticles were dispersed in an aqueous solution to form a silver nanoparticle aqueous solution with a concentration of 8.6mg/mL. Then a nanosilver SERS substrate was prepared according to the above method and a melamine aqueous solution of the same concentration was detected.
  • the SERS substrate prepared from the broccoli-like micro-nano silver prepared in Examples 1 to 3 has excellent and extensive Raman enhancement effects. Compared with the SERS substrate prepared from purchased spherical silver nanoparticles, Its amplification effect on the Raman spectrum signal of sample molecules is more obvious.
  • the specific process is as follows: first prepare a silver nitrate solution with a concentration of 0.8 mol/L, and then drop ammonia water into it to prepare a silver ammonia solution;
  • the purchased spherical silver nanoparticles were dispersed in an aqueous solution to prepare a nanosilver particle aqueous solution with a concentration of 2.16 mg/mL, and then a nanosilver SERS substrate was prepared according to the above method to detect the same concentration of rhodamine 6G. aqueous solution.
  • the specific process is as follows: first prepare a silver nitrate solution with a concentration of 0.9 mol/L, and then drop ammonia water into it to prepare a silver ammonia solution;
  • the broccoli dropped The volume of the micro-nano silver dispersion is the same as the volume of the dropped sample solution to be tested, both 40 ⁇ L; the laser wavelength selected for the test is 785nm, the integration time is 10s, the laser power is 5mW, and the laser spot is 1um
  • the purchased spherical silver nanoparticles were dispersed in an aqueous solution to form a silver nanoparticle aqueous solution with a concentration of 6.5 mg/mL, and then a nanosilver SERS substrate was prepared according to the above method to detect the same concentration of malachite green. aqueous solution.
  • the specific process is as follows: first prepare a silver nitrate solution with a concentration of 1.2 mol/L, and then add ammonia water dropwise therein to prepare a silver ammonia solution;
  • the dropped broccoli-like micro-nano silver The volume of the dispersion is the same as the volume of the dropped sample solution to be tested, both 40 ⁇ L; the laser wavelength selected for the test is 785nm, the integration time is 10s, the laser power is 5mW, and the laser spot is 1um
  • the purchased spherical silver nanoparticles were dispersed in an aqueous solution to prepare a silver nanoparticle aqueous solution with a concentration of 10.8 mg/mL. Then a nanosilver SERS substrate was prepared according to the above method to detect an aqueous melamine solution of the same concentration.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Physics & Mathematics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Nanotechnology (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)

Abstract

一种西兰花状微纳米银的制备方法及其应用，制备方法：分别配置浓度为2-3mg/mL的酚酸类化合物水溶液以及浓度为0.8-1.2mol/L的银氨溶液，向酚酸类化合物水溶液内滴加银氨溶液后，先搅拌15-20min，再在25-30℃下以80-100KHz的超声频率超声反应60-90min，制得西兰花状微纳米银，其中，酚酸类化合物水溶液与银氨溶液的体积比为67:1；应用：将西兰花状微纳米银的分散液滴加在载玻片上后晾干制成用于检测罗丹明6G、三聚氰胺或孔雀石绿的SERS基底。制备过程环保，没有引入其它有害的化学试剂，产品应用于拉曼信号的检测，精确快速。

Description

一种西兰花状微纳米银的制备方法及其应用 技术领域
本发明属于新材料及表面增强拉曼光检测领域，涉及一种西兰花状微纳米银的制备方法及其应用。
背景技术
金属纳米结构具有更为丰富、稳定的化学和物理性质，因此纳米尺度金属结构的制备将成为纳米材料领域的一大研究热点。花状微纳米银属于贵金属纳米材料中的一种，由于其独特的尺寸与形貌，在抗菌性、导电性、光学性等方面呈现出优良的性能，可广泛应用于化学催化、表面增强拉曼和光电子器件等领域。
随着近年来多酚化学的发展，多酚物质在医药制备、工业涂层、材料功能改性等领域逐渐显现出应用价值。咖啡酸属于天然多酚中的一种，其具有良好的抗炎、抗菌、抗病毒等药理作用，同时也是良好的绿色还原剂，而有关其在制备三维微纳米银结构方面鲜有文献报道。
近些年来，大量工业废水的排放以及农药、兽药的滥用极大地影响到环境安全、食品安全和人体健康等方面，因此，实施快速、有效的环境监测，食品安全监测是十分有必要的。目前，常见的检测手段有高效液相色谱、气相色谱、液相色谱质谱，以及比色法等。这些方法准确、适用广泛，但需要昂贵的设备和熟练的操作，而且耗时。此外，比色法由于操作过程中易受到基质以及其它添加物质信号的影响，所有常常还需要一个较为复杂的样品预处理过程，这极大地限制了这些方法在实际现场中应用。
表面增强拉曼散射光谱是一种快速、非破坏性等特点的物质结构分析手段，在生物监测，环境监测，食品安全检测等领域具有实际而广泛的应用。目前，表面增强拉曼基底大多是基于贵金属的纳米结构或纳米粗糙表面，以增强局域电磁场强度，进而放大贵金属纳米结构周围待测样品分子的拉曼散射信号。贵金属纳米结构的制备方法包括物理刻蚀法、化学合成法、光诱导法、电化学法及生物法，其中化学还原法合成的金属纳米结构多样化，自身缺陷少，操作较为简便，是制备纳米结构的常用方法之一。但是目前多数化学法需要引入较多的化学试剂，存在生产成本较高、环境污染等问题。
因此，寻求一种节能减排且绿色环保的制备工艺以制备表面增强拉曼基底是十分有必要的。
发明内容
本发明的目的是解决现有技术中存在的问题，提供一种西兰花状微纳米银的制备方法及其应用。
为了达到上述目的，本发明的技术方案如下：
一种西兰花状微纳米银的制备方法，分别配置浓度为2-3mg/mL的酚酸类化合物水溶液以及浓度为0.8-1.2mol/L的银氨溶液，向所述酚酸类化合物水溶液内滴加所述银氨溶液后，先搅拌15-20min，再在25-30℃下以80-100KHz的超声频率超声反应60-90min，制得西兰花状微纳米银，其中，酚酸类化合物 水溶液与银氨溶液的体积比为67:1；反应结束后，制得西兰花状微纳米银需要离心分离，用乙醇，去离子水清洗，重复离心、清洗步骤3-4次；
酚酸类化合物酚结构中由于苯环以及苯环侧链上双键的存在，分子中具有一个大共轭体系，且由于羧基的存在，使得共轭体系吸电子能力较大。在酚羟基C-O-H结构中，氧原子含有孤对p电子，p电子云和共轭体系中大π电子云从侧面有所重叠，由于大共轭体系吸电子效应，使得氧原子上的p电子云向苯环转移，氢、氧原子间的电子云向氧原子方向转移，酚羟基上的O-H键倾向断裂，生成邻苯二醌结构，其中，小分子酚酸类化合物酚羟基上的O-H键的解离能(BED)通常在200-400kJ/mol左右。此时，以具有足够强度的80-100KHz的超声频率超声处理反应溶液，溶液中发生“声空化”效应，瞬间释放5000K以上的高温，5.05×10 8Pa以上的高压以及速率高于110m/s的强冲击微射流，这些能量(只要确保超声频率为80-100KHz就能确保产生这些能量)能够打开键能在370-420KJ/mol左右的化学键，足以使酚羟基中O-H键断裂，促进氢原子离去，醌式结构形成。与此同时，小分子酚酸类化合物中的羧基负离子通过静电络合从溶液里捕获带正电的Ag +，形成相对稳定的配合物，原先在共轭环和侧链双键之间自由移动的电子受到静电力影响逐渐被吸引靠近Ag +，Ag +捕获得到电子，被还原成银原子并被释放。溶液里银原子不断聚合成银晶核(小部分银晶核是在超声之前的形成的，大部分银晶核是在超声之后形成的，因为超声之前搅拌了15-20min，这个过程会有银原子被还原，然后形成银晶核，只是相比于后续超声过程，这个过程相对温和，还原速率较慢，短时间形成的银晶核数量较少，后续超声过程还会有更多银原子被不断还原出，形成银晶核。总的来说，超声反应之前的搅拌过程主要是为了使还原剂和银源能够混合均匀，充分接触，当然这个过程也伴随着银源被还原，形成晶核，只是条件温和，短时间内，还原出的银原子有限，形成的晶核有限。)，由于小分子酚酸类化合物被氧化成醌式结构后，结构中C＝O会在银晶核(100)面发生微弱的吸附作用，银晶核(100)面出现钝化现象，所以银晶核在团聚生长时具有各向异性特征，逐渐生成类似二维瓣状结构。伴随着声空化效应，体系能量上升，溶液中二维瓣状银结构获得更多动能，在溶液中快速无规则地运动，相互碰撞缔结，形成三维银花苞结构。随着超声时间变长，三维银花苞的数量进一步增多，直至超过临界团聚浓度(本发明通过控制酚酸类化合物水溶液浓度、银氨溶液浓度、酚酸类化合物水溶液与银氨溶液的体积比、超声之前的搅拌时间、超声温度、超声频率、超声反应时间确保超声反应结束前三维银花苞的数量能够超过临界团聚浓度)，一个个三维银花苞便随机地与各方向相邻的花苞继续聚集形成近花簇状的银微粒，花状银结构基本形成。与此同时，声空化现象产生的冲击波和微射流不断击打上述银花瓣、银花苞以及银花簇表面，遭到击打多的部位逐渐变得凹陷，遭到击打少的部位形状变化不大，表面粗糙度增加，出现大量更小量度级凹凸不平的结构，银花簇表面形态得到进一步修饰，形成近似西兰花状银微粒。
作为优选的技术方案：
如上所述的一种西兰花状微纳米银的制备方法，所述酚酸类化合物为咖啡酸、阿魏酸或绿原酸。
如上所述的一种西兰花状微纳米银的制备方法，所述银氨溶液的配置过程为：先配置浓度为0.8-1.2mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液。
如上所述的一种西兰花状微纳米银的制备方法，所述搅拌的速度为200-300r/min，搅拌是为了使还原剂和银源混合均匀，接触充分，搅拌的速度的设置只要能保证达到上述目的即可。
如上所述的一种西兰花状微纳米银的制备方法，所述搅拌在26±2℃的温度条件下进行。
本发明还提供一种西兰花状微纳米银的应用，将西兰花状微纳米银的分散液滴加在载玻片上后晾干制成用于检测罗丹明6G、三聚氰胺或孔雀石绿的SERS基底，其中西兰花状微纳米银采用如上任一项所述的制备方法制得。
作为优选的技术方案：
如上所述的一种西兰花状微纳米银的应用，检测罗丹明6G、三聚氰胺或孔雀石绿的过程为：将罗丹明6G、三聚氰胺或孔雀石绿配置成待测样品溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试。
如上所述的一种西兰花状微纳米银的应用，西兰花状微纳米银的分散液的浓度为2.16-10.8mg/L，待测样品溶液的浓度为10 -4-10 -10mol/L，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同。
如上所述的一种西兰花状微纳米银的应用，测试选用的激光波长为785nm。
本发明的原理如下：
酚酸类化合物能够很容易地从溶液里捕获带正电的Ag离子，并与其形成相对稳定的配合物。然而，由于酚酸类化合物具有还原性，被捕获在配合物中的银离子会被酚酸类化合物还原为银原子并释放。银原子开始缓慢且不均匀地成核。随着反应的不断进行，银原子开始聚集成初级银晶体。银前驱体数量进一步增加，更多的银原子处于逐渐沉积的过程中，形成了具有不同表面粗糙度的分级Ag颗粒。此外，超声处理可以产生声空化，从而加速反应，促进三维花状银微观结构的形成。
有益效果
(1)本发明的制备方法，没有引入其它有害的化学试剂，环保节能；
(2)与单纯使用化学还原法制备金属纳米结构相比，本发明的制备方法将化学还原法与物理方法结合，避免了引入较多的化学试剂，一定程度上可以降低生产成本、减少环境污染；
(3)本发明制得的一种西兰花状微纳米银的表面具有层层微凸结构，在激光照射下能够提供更多的SERS热点，具有更加优异的表面增强拉曼信号法能力，可以更精确、灵敏、便捷，实时快速地实现拉曼信号检测；
附图说明
图1为实施例1中制得的西兰花状微纳米银的SEM图；
图2为实施例2中制得的西兰花状微纳米银的SEM图；
图3为实施例1制得的西兰花状微纳米银与购买的球状银纳米颗粒分别对罗丹明6G的表面增强拉曼光谱图；
图4为实施例2制得的西兰花状微纳米银与购买的球状银纳米颗粒分别对孔雀石绿的表面增强拉曼光谱图；
图5为实施例3制得的西兰花状微纳米银与购买的球状银纳米颗粒分别对三聚氰胺的表面增强拉曼光谱图。
具体实施方式
下面结合具体实施方式，进一步阐述本发明。应理解，这些实施例仅用于说明本发明而不用于限制本发明的范围。此外应理解，在阅读了本发明讲授的内容之后，本领域技术人员可以对本发明作各种改动或修改，这些等价形式同样落于本申请所附权利要求书所限定的范围。
以下各实施例中，球状银纳米颗粒的货号为S196425-25g，源自苏州格瑞特医药技术有限公司。
实施例1
一种西兰花状微纳米银的制备方法，具体步骤如下：
(1)原料的准备；
配置浓度为2.4mg/mL的咖啡酸水溶液；
配置浓度为1mol/L的银氨溶液，具体过程为：先配置浓度为1mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液；
(2)按照67:1的体积比向咖啡酸水溶液内滴加银氨溶液后，在26℃的温度条件下，以250r/min的搅拌速度，先搅拌15min，再在30℃下以80KHz的超声频率超声反应80min，制得西兰花状微纳米银，如图1所示，为制得的西兰花状微纳米银的扫描电镜图，西兰花状微纳米银的直径为300-500nm。
应用：先将西兰花状微纳米银分散在水中，配置成浓度为4.3mg/L西兰花状微纳米银分散液，然后滴加在载玻片上后晾干制成用于检测罗丹明6G的SERS基底，接着将罗丹明6G配置成浓度为10 -4mol/L的待测样品水溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试，其中，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同，都为30μL；测试选用的激光波长为785nm，积分时间为10s，激光功率为5mW，激光光斑为1um。
同理，为了对比，取购买的球状银纳米颗粒分散于水溶液中，配置成浓度为4.3mg/mL的纳米银颗粒水溶液，然后按照上述方法制备成纳米银SERS基底，检测同等浓度的罗丹明6G水溶液。
对比例1
一种纳米银的制备方法，基本同实施例1，不同之处仅在于超声频率为110KHz。
最终制得的纳米银的形状为表面较为光滑的花状，直径为200-400nm。
将实施例1与对比例1对比可以看出，超声频率对最终产品的形貌影响较大，超声频率过大会导致空化气泡生长周期短，空化气泡数量增多，但体积变小，空化气泡崩溃时所释放的瞬间能量变小，给予银原子运动的动能也变少，所以形成的纳米银结构直径变小了些。同时，由于空化气泡体积变小，形成的冲击波和微射流冲击力变小，对银花瓣、银花苞以及银花簇表面击打变弱，表面粗糙，凹凸不平的现象不那么明显，相对更光滑。
对比例2
一种纳米银的制备方法，基本同实施例1，不同之处仅在于超声频率为70KHz。
最终制得的纳米银的形状为不规则球状，直径为700-800nm。
将实施例1与对比例2对比可以看出，超声频率对最终产品的形貌影响较大，超声频率过小会导致空化气泡在爆破之前能生成较大尺寸的空化气泡，空化气泡体积变大，崩溃时所释放的瞬间能量变大，给予银离子，银原子运动的动能变多，增加了银离子被还原的速率，也加快了银原子聚合的速度，生成具有较大直径颗粒状银聚集体，同时，由于空化气泡体积变大，空化强度大，形成的冲击波和微射流冲击力变强，对银花瓣、银花苞以及银花簇表面击打变强，由于低频率下，空化气泡生长时间较长，所以对纳米银表面机械击打的次数没有高频率下空化气泡对纳米银表面击打的那么频繁而规律，所以低频率下纳米银表面凹凸不平的现象会很明显，不规则。
对比例3
一种纳米银的制备方法，基本同实施例1，不同之处仅在于还原剂为硼氢化钠，而不再是咖啡酸。
最终制得的纳米银的形状为不规则块状，直径为800-1000nm。
将实施例1与对比例3对比可以看出，还原剂的种类对最终产品的形貌影响较大，硼氢化钠还原性比酚酸类要强的多，银离子被迅速还原成银单质，随后，快速团聚，聚集，沉淀，形成较大体积的块状。
实施例2
一种西兰花状微纳米银的制备方法，具体步骤如下：
(1)原料的准备；
配置浓度为2.5mg/mL的咖啡酸水溶液；
配置浓度为1mol/L的银氨溶液，具体过程为：先配置浓度为1mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液；
(2)按照67:1的体积比向咖啡酸水溶液内滴加银氨溶液后，在26℃的温度条件下，以300r/min的 搅拌速度，先搅拌20min，再在25℃下以90KHz的超声频率超声反应80min，制得西兰花状微纳米银，如图2所示，为西兰花状微纳米银的扫描电镜图。
应用：先将西兰花状微纳米银分散在水中，配置成浓度为6.5mg/L西兰花状微纳米银分散液，然后滴加在载玻片上后晾干制成用于检测孔雀石绿的SERS基底，接着将孔雀石绿配置成浓度为10 -4mol/L的待测样品水溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试，其中，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同，都为30μL；测试选用的激光波长为785nm，积分时间为10s，激光功率为5mW，激光光斑为1um。
同理，为了对比，取购买的球状银纳米颗粒分散于水溶液中，配置成浓度为6.5mg/mL的纳米银颗粒水溶液，然后按照上述方法制备成纳米银SERS基底，检测同等浓度的孔雀石绿水溶液。
实施例3
一种西兰花状微纳米银的制备方法，具体步骤如下：
(1)原料的准备；
配置浓度为2.6mg/mL的咖啡酸水溶液；
配置浓度为1mol/L的银氨溶液，具体过程为：先配置浓度为1mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液；
(2)按照67:1的体积比向咖啡酸水溶液内滴加银氨溶液后，在28℃的温度条件下，以300r/min的搅拌速度，先搅拌20min，再在28℃下以100KHz的超声频率超声反应90min，制得西兰花状微纳米银。
应用：先将西兰花状微纳米银分散在水中，配置成浓度为8.6mg/L西兰花状微纳米银分散液，然后滴加在载玻片上后晾干制成用于检测三聚氰胺的SERS基底，接着将三聚氰胺配置成浓度为10 -4mol/L的待测样品水溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试，其中，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同，都为30μL；测试选用的激光波长为785nm，积分时间为10s，激光功率为5mW，激光光斑为1um。
同理，为了对比，取购买的球状银纳米颗粒分散于水溶液中，配置成浓度为8.6mg/mL的纳米银颗粒水溶液，然后按照上述方法制备成纳米银SERS基底，检测同等浓度的三聚氰胺水溶液。
如图3～5所示，实施例1～3所制备的西兰花状微纳米银制备的SERS基底具有优异而广泛的拉曼增强效应，相比于购买的球状银纳米颗粒制备的SERS基底，其对样品分子的拉曼光谱信号放大效果更加明显。
实施例4
一种西兰花状微纳米银的制备方法，具体步骤如下：
(1)原料的准备；
配置浓度为2mg/mL的阿魏酸水溶液；
配置浓度为0.8mol/L的银氨溶液，具体过程为：先配置浓度为0.8mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液；
(2)按照67:1的体积比向阿魏酸水溶液内滴加银氨溶液后，在27℃的温度条件下，以200r/min的搅拌速度，先搅拌16min，再在25℃下以85KHz的超声频率超声反应60min，制得西兰花状微纳米银。
应用：先将西兰花状微纳米银分散在水中，配置成浓度为2.16mg/L西兰花状微纳米银分散液，然后滴加在载玻片上后晾干制成用于检测罗丹明6G的SERS基底，接着将罗丹明6G配置成浓度为10 -6mol/L的待测样品水溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试，其中，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同，都为35μL；测试选用的激光波长为785nm，积分时间为10s，激光功率为5mW，激光光斑为1um。
同理，为了对比，取购买的球状银纳米颗粒分散于水溶液中，配置成浓度为2.16mg/mL的纳米银颗粒水溶液，然后按照上述方法制备成纳米银SERS基底，检测同等浓度的罗丹明6G水溶液。
实施例5
一种西兰花状微纳米银的制备方法，具体步骤如下：
(1)原料的准备；
配置浓度为2.5mg/mL的绿原酸水溶液；
配置浓度为0.9mol/L的银氨溶液，具体过程为：先配置浓度为0.9mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液；
(2)按照67:1的体积比向绿原酸水溶液内滴加银氨溶液后，在28℃的温度条件下，以230r/min的搅拌速度，先搅拌17min，再在30℃下以95KHz的超声频率超声反应70min，制得西兰花状微纳米银。
应用：先将西兰花状微纳米银分散在水中，配置成浓度为6.5mg/L西兰花状微纳米银分散液，然后滴加在载玻片上后晾干制成用于检测孔雀石绿的SERS基底，接着将孔雀石绿配置成浓度为10 -8mol/L的待测样品水溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试，其中，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同，都为40μL；测试选用的激光波长为785nm，积分时间为10s，激光功率为5mW，激光光斑为1um
同理，为了对比，取购买的球状银纳米颗粒分散于水溶液中，配置成浓度为6.5mg/mL的纳米银颗粒水溶液，然后按照上述方法制备成纳米银SERS基底，检测同等浓度的孔雀石绿水溶液。
实施例6
一种西兰花状微纳米银的制备方法，具体步骤如下：
(1)原料的准备；
配置浓度为3mg/mL的绿原酸水溶液；
配置浓度为1.2mol/L的银氨溶液，具体过程为：先配置浓度为1.2mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液；
(2)按照67:1的体积比向绿原酸水溶液内滴加银氨溶液后，在30℃的温度条件下，以280r/min的搅拌速度，先搅拌18min，再在27℃下以100KHz的超声频率超声反应80min，制得西兰花状微纳米银。
应用：先将西兰花状微纳米银分散在水中，配置成浓度为10.8mg/L西兰花状微纳米银分散液，然后滴加在载玻片上后晾干制成用于检测三聚氰胺的SERS基底，接着将三聚氰胺配置成浓度为10 -10mol/L的待测样品水溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试，其中，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同，都为40μL；测试选用的激光波长为785nm，积分时间为10s，激光功率为5mW，激光光斑为1um
同理，为了对比，取购买的球状银纳米颗粒分散于水溶液中，配置成浓度为10.8mg/mL的纳米银颗粒水溶液，然后按照上述方法制备成纳米银SERS基底，检测同等浓度的三聚氰胺水溶液。

Claims (9)

  1. 一种西兰花状微纳米银的制备方法，其特征在于，分别配置浓度为2-3mg/mL的酚酸类化合物水溶液以及浓度为0.8-1.2mol/L的银氨溶液，向所述酚酸类化合物水溶液内滴加所述银氨溶液后，先搅拌15-20min，再在25-30℃下以80-100KHz的超声频率超声反应60-90min，制得西兰花状微纳米银，其中，酚酸类化合物水溶液与银氨溶液的体积比为67:1。
  2. 根据权利要求1所述的一种西兰花状微纳米银的制备方法，其特征在于，所述酚酸类化合物为咖啡酸、阿魏酸或绿原酸。
  3. 根据权利要求1所述的一种西兰花状微纳米银的制备方法，其特征在于，所述银氨溶液的配置过程为：先配置浓度为0.8-1.2mol/L的硝酸银溶液，再向其中滴加氨水制备成银氨溶液。
  4. 根据权利要求1所述的一种西兰花状微纳米银的制备方法，其特征在于，所述搅拌的速度为200-300r/min。
  5. 根据权利要求1所述的一种西兰花状微纳米银的制备方法，其特征在于，所述搅拌在26±2℃的温度条件下进行。
  6. 一种西兰花状微纳米银的应用，其特征在于，将西兰花状微纳米银的分散液滴加在载玻片上后晾干制成用于检测罗丹明6G、三聚氰胺或孔雀石绿的SERS基底，其中西兰花状微纳米银采用如权利要求1～5任一项所述的制备方法制得。
  7. 根据权利要求6所述的一种西兰花状微纳米银的应用，其特征在于，检测罗丹明6G、三聚氰胺或孔雀石绿的过程为：将罗丹明6G、三聚氰胺或孔雀石绿配置成待测样品溶液后滴加在SERS基底上后晾干，置于拉曼光谱仪下进行测试。
  8. 根据权利要求7所述的一种西兰花状微纳米银的应用，其特征在于，西兰花状微纳米银的分散液的浓度为2.16-10.8mg/L，待测样品溶液的浓度为10 -4-10 -10mol/L，滴加的西兰花状微纳米银的分散液的体积与滴加的待测样品溶液的体积相同。
  9. 根据权利要求7所述的一种西兰花状微纳米银的应用，其特征在于，测试选用的激光波长为785nm。
PCT/CN2022/109869 2022-05-20 2022-08-03 一种西兰花状微纳米银的制备方法及其应用 WO2023221298A1 (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN202210553875.9 2022-05-20
CN202210553875.9A CN114888299B (zh) 2022-05-20 2022-05-20 一种西兰花状微纳米银的制备方法及其应用

Publications (1)

Publication Number Publication Date
WO2023221298A1 true WO2023221298A1 (zh) 2023-11-23

Family

ID=82723176

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2022/109869 WO2023221298A1 (zh) 2022-05-20 2022-08-03 一种西兰花状微纳米银的制备方法及其应用

Country Status (2)

Country Link
CN (1) CN114888299B (zh)
WO (1) WO2023221298A1 (zh)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115464148B (zh) * 2022-09-21 2023-05-26 广东石油化工学院 一种花瓣状微纳米银粉的制备方法
CN116833418A (zh) * 2023-03-02 2023-10-03 深圳市哈深智材科技有限公司 一种空心结构类菜花状金属银粉及制备方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006063414A (ja) * 2004-08-27 2006-03-09 Mitsui Mining & Smelting Co Ltd 球状高粗度銀粒子を含む銀粉、フレーク状高粗度銀粒子を含む銀粉、球状高粗度銀粒子を含む銀粉とフレーク状高粗度銀粒子を含む銀粉との混合粉、及び、これら銀粉の製造方法、当該銀粉を含有する銀インク及び銀ペースト、並びに、当該銀粉の製造方法
CN102221543A (zh) * 2011-06-01 2011-10-19 中国科学院合肥物质科学研究院 三维银微纳米结构表面增强拉曼活性基底的制备方法
CN107127355A (zh) * 2017-07-04 2017-09-05 广东工业大学 一种花状银纳米球、其制备方法及其应用
CN109128211A (zh) * 2018-08-16 2019-01-04 山东大学 水溶液体系中制备微纳米银颗粒的方法
US20210070629A1 (en) * 2019-09-05 2021-03-11 Imam Abdulrahman Bin Faisal University Green synthesis of noble metal/transition metal oxide nanocomposite

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101786170B (zh) * 2010-03-26 2011-09-14 上海师范大学 具表面增强拉曼散射活性的菜花状纳米金-银合金的制备方法
CN103273079B (zh) * 2013-05-10 2015-07-22 安徽医科大学 一种金纳米花的制备方法及其应用
CN103302306A (zh) * 2013-06-19 2013-09-18 东南大学 一种基于多酚还原制备功能化纳米银的方法
CN103551585A (zh) * 2013-07-17 2014-02-05 苏州正业昌智能科技有限公司 一种采用柿单宁为还原剂的纳米银的制备方法
CN104259481A (zh) * 2014-10-14 2015-01-07 钱景 一种纳米银的制备方法
CN104227018A (zh) * 2014-10-14 2014-12-24 钱景 一种纳米银的绿色制备方法
CN104690265B (zh) * 2015-03-17 2017-05-10 福州大学 一种金纳米星及其制备方法和应用
CN105033279A (zh) * 2015-08-22 2015-11-11 赵兵 一种咖啡酸片制备纳米银及其抗菌织物的方法
CN106392098A (zh) * 2016-10-10 2017-02-15 苏州经贸职业技术学院 纳米银水溶胶的制备方法及染料废水的处理方法
CN110076349B (zh) * 2019-06-13 2022-02-18 江苏汇诚医疗科技有限公司 一种花瓣状银纳米片的绿色制备方法
CN110227816B (zh) * 2019-07-15 2021-11-02 福州大学 一种具有核壳结构的金银纳米花颗粒及其制备方法和应用
KR102292488B1 (ko) * 2020-05-25 2021-08-24 대진대학교 산학협력단 감귤과 식물을 이용한 은 나노입자의 제조 방법
CN111673090B (zh) * 2020-06-09 2022-12-20 中北大学 一种以没食子酸为结构导向剂的花状银制备方法
CN113000854A (zh) * 2021-02-24 2021-06-22 杭州电子科技大学 一种褐藻提取物制备纳米银的方法
CN113523297B (zh) * 2021-07-13 2023-04-18 广州萃普生物科技有限公司 一种利用牡丹提取物制备纳米银的方法
CN113621153A (zh) * 2021-08-05 2021-11-09 集美大学 一种植物提取物合成纳米银多功能可降解食品包装材料及其制备方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006063414A (ja) * 2004-08-27 2006-03-09 Mitsui Mining & Smelting Co Ltd 球状高粗度銀粒子を含む銀粉、フレーク状高粗度銀粒子を含む銀粉、球状高粗度銀粒子を含む銀粉とフレーク状高粗度銀粒子を含む銀粉との混合粉、及び、これら銀粉の製造方法、当該銀粉を含有する銀インク及び銀ペースト、並びに、当該銀粉の製造方法
CN102221543A (zh) * 2011-06-01 2011-10-19 中国科学院合肥物质科学研究院 三维银微纳米结构表面增强拉曼活性基底的制备方法
CN107127355A (zh) * 2017-07-04 2017-09-05 广东工业大学 一种花状银纳米球、其制备方法及其应用
CN109128211A (zh) * 2018-08-16 2019-01-04 山东大学 水溶液体系中制备微纳米银颗粒的方法
US20210070629A1 (en) * 2019-09-05 2021-03-11 Imam Abdulrahman Bin Faisal University Green synthesis of noble metal/transition metal oxide nanocomposite

Also Published As

Publication number Publication date
CN114888299B (zh) 2023-04-18
CN114888299A (zh) 2022-08-12

Similar Documents

Publication Publication Date Title
WO2023221298A1 (zh) 一种西兰花状微纳米银的制备方法及其应用
Zhu et al. A facile preparation method for new two-component supramolecular hydrogels and their performances in adsorption, catalysis, and stimuli-response
Liang et al. Controlled synthesis of uniform silver nanospheres
Yang et al. Hydrogen-bond-mediated in situ fabrication of AgNPs/Agar/PAN electrospun nanofibers as reproducible SERS substrates
Shi et al. Aptasensor based on tripetalous cadmium sulfide-graphene electrochemiluminescence for the detection of carcinoembryonic antigen
Ma et al. Colorimetric immunosensor based on Au@ g-C3N4-doped spongelike 3D network cellulose hydrogels for detecting α-fetoprotein
Li et al. Molecular hot spots in surface-enhanced Raman scattering
CN106706598B (zh) 一种拉曼增强剂的制备及应用
CN103219090B (zh) 一种纳米银包覆高分子微球复合导电银浆的制备方法
CN104198464A (zh) 一种表面增强拉曼散射检测体系的构建方法
CN106623894B (zh) 磁性复合颗粒及其制备方法和应用
CN102706856B (zh) 一种增强拉曼纳米粒子及其制备方法
CN107084968A (zh) 一种利用分子模板增强试剂提升sers基底检测灵敏度的方法
Zhu et al. Self-assembled Ag nanoparticles for surface enhanced Raman scattering
He et al. Magnetoresponsive nanozyme: magnetic stimulation on the nanozyme activity of iron oxide nanoparticles
CN111426674B (zh) 一种增强sers活性的太阳花纳米阵列结构及其制备方法
Song et al. Fabrication of Fe3O4@ Ag magnetic nanoparticles for highly active SERS enhancement and paraquat detection
Zhang et al. Recyclable surface-enhanced Raman scattering substrate-based sensors for various applications
Zhang et al. Laser reshaping of gold nanoparticles for highly sensitive SERS detection of ciprofloxacin
Mutharani et al. Ultrasound-induced radicals initiated the formation of inorganic–organic Pr2O3/polystyrene hybrid composite for electro-oxidative determination of chemotherapeutic drug methotrexate
CN109975271B (zh) 高重现性表面增强拉曼散射的基底材料及其使用方法
Yadav et al. The current state of the art of plasmonic nanofibrous mats as SERS substrates: design, fabrication and sensor applications
Lu et al. Improved SERS performance of a silver triangular nanoparticle/TiO 2 nanoarray heterostructure and its application for food additive detection
Hu et al. Tailoring size and coverage density of silver nanoparticles on monodispersed polymer spheres as highly sensitive SERS substrates
CN108645837B (zh) 一种Ag@NGO复合纳米材料的制备方法及其应用

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 22942329

Country of ref document: EP

Kind code of ref document: A1