CN106199681A - A kind of nuclear reaction radiation conversion target and preparation method thereof and a kind of offset-type neutron detector - Google Patents

A kind of nuclear reaction radiation conversion target and preparation method thereof and a kind of offset-type neutron detector Download PDF

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CN106199681A
CN106199681A CN201610478698.7A CN201610478698A CN106199681A CN 106199681 A CN106199681 A CN 106199681A CN 201610478698 A CN201610478698 A CN 201610478698A CN 106199681 A CN106199681 A CN 106199681A
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conversion target
radiation conversion
nuclear reaction
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substrate
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CN106199681B (en
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宋晓靓
李达
张小东
孙光智
余小任
苗亮亮
苏春磊
马燕
刘志勇
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Northwest Institute of Nuclear Technology
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    • G01MEASURING; TESTING
    • G01TMEASUREMENT OF NUCLEAR OR X-RADIATION
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    • G01T3/06Measuring neutron radiation with scintillation detectors

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Abstract

本发明提供了一种核反应辐射转换靶的制备方法,本发明提供的制备方法可操作性强,通过简单的操作步骤即可制备得到均匀性好且性能稳定的核反应辐射转换靶。本发明提供了一种核反应辐射转换靶,本发明提供的核反应辐射转换靶能够在快中子能区实现能量响应补偿,应用于补偿型中子探测器中,有利于在中子总数测量过程中保持较平坦的能量响应、较高的中子灵敏度和n/γ分辨能力,为精确地测量低强度脉冲中子源的中子总数奠定了基础。理论计算和实验结果表明,包括本发明提供的核反应辐射转换靶的补偿型中子探测器,中子能量在1~15MeV区间时,其能量响应在1.01~1.44范围内,中子灵敏度为10‑15C·cm,n/γ≥5。

The invention provides a method for preparing a nuclear reaction radiation conversion target. The preparation method provided by the invention has strong operability, and the nuclear reaction radiation conversion target with good uniformity and stable performance can be prepared through simple operation steps. The invention provides a nuclear reaction radiation conversion target. The nuclear reaction radiation conversion target provided by the invention can realize energy response compensation in the fast neutron energy region, and is applied in a compensation type neutron detector, which is beneficial in the process of measuring the total number of neutrons It maintains relatively flat energy response, high neutron sensitivity and n/γ resolution, which lays the foundation for accurately measuring the total neutrons of low-intensity pulsed neutron sources. Theoretical calculations and experimental results show that the compensating neutron detector comprising the nuclear reaction radiation conversion target provided by the present invention, when the neutron energy is in the range of 1-15 MeV, its energy response is in the range of 1.01-1.44, and the neutron sensitivity is 10 ‑ 15 C cm, n/γ≥5.

Description

一种核反应辐射转换靶及其制备方法和一种补偿型中子探 测器A nuclear reaction radiation conversion target and its preparation method and a compensation type neutron detector detector

技术领域technical field

本发明涉及中子探测技术领域,特别涉及一种核反应辐射转换靶及其制备方法和一种补偿型中子探测器。The invention relates to the technical field of neutron detection, in particular to a nuclear reaction radiation conversion target, a preparation method thereof and a compensation type neutron detector.

背景技术Background technique

中子总数测量是低强度脉冲辐射探测的一项重要内容,低强度脉冲中子源具有中子强度低、中子能量范围宽、脉冲持续时间短、中子与伽马射线混合严重等特点。因此要精确地测量低强度脉冲中子源的中子总数,需要中子探测器具有较高的中子灵敏度、较平坦的能量响应、较高的n/γ分辨能力和较快的时间响应等性能。在低强度脉冲中子探测中,用于中子总数测量的探测器主要有闪烁薄膜中子探测器、闪烁纤维阵列中子探测器、狭缝式裂变中子探测器和补偿法中子探测器。The total number of neutrons is an important part of low-intensity pulsed radiation detection. Low-intensity pulsed neutron sources have the characteristics of low neutron intensity, wide neutron energy range, short pulse duration, and serious mixing of neutrons and gamma rays. Therefore, to accurately measure the total number of neutrons in low-intensity pulsed neutron sources, neutron detectors are required to have higher neutron sensitivity, flatter energy response, higher n/γ resolution and faster time response, etc. performance. In the detection of low-intensity pulsed neutrons, the detectors used to measure the total number of neutrons mainly include scintillation film neutron detectors, scintillation fiber array neutron detectors, slit fission neutron detectors and compensation neutron detectors .

闪烁薄膜中子探测器是利用光电倍增管探测中子在有机薄膜闪烁体中产生的反冲质子激发闪烁体发光来实现对中子的测量,具有时间响应快、中子灵敏较高等优点。然而,由于有机闪烁体对电子的发光效率比对质子高,这使得有机闪烁体对γ射线的灵敏度也很高,因而其n/γ分辨能力不高。闪烁纤维阵列中子探测器是利用光电倍增管探测中子在纤维闪烁体产生的反冲质子激发闪烁体发光来实现对中子的测量,中子灵敏度较高,但是其能谱响应不够平坦,导致n/γ分辨能力不够好。狭缝式裂变中子探测器是利用PIN探测中子诱发裂变靶裂变产生的裂变碎片来测量中子,具有能量响应平坦的优点。然而为了降低n、γ直照信号的影响,需要将PIN探测器偏离辐射通道布置,导致只能探测到很少一部分裂变碎片,因此其中子灵敏度较低,约为10-17~10-20C·cm,不能满足低强度脉冲中子辐射场的测量要求。Scintillation thin-film neutron detectors use photomultiplier tubes to detect neutrons in organic thin-film scintillators, and the recoil protons generated in organic thin-film scintillators excite the scintillator to measure neutrons. It has the advantages of fast time response and high neutron sensitivity. However, since the luminescence efficiency of organic scintillators for electrons is higher than that for protons, the sensitivity of organic scintillators to γ-rays is also high, so their n/γ resolution is not high. Scintillation fiber array neutron detectors use photomultiplier tubes to detect neutrons. The recoil protons generated by the fiber scintillator excite the scintillator to emit light to realize the measurement of neutrons. The neutron sensitivity is high, but its energy spectrum response is not flat enough. The resulting n/γ resolution is not good enough. The slit fission neutron detector uses PIN to detect the fission fragments produced by neutron-induced fission target fission to measure neutrons, which has the advantage of flat energy response. However, in order to reduce the influence of n and γ direct illumination signals, it is necessary to arrange the PIN detector away from the radiation channel, so that only a small part of the fission fragments can be detected, so the neutron sensitivity is low, about 10 -17 ~ 10 -20 C cm, which cannot meet the measurement requirements of low-intensity pulsed neutron radiation field.

补偿法中子探测器是利用PIN测量的总信号电流减去另一个PIN测量的n、γ直照信号电流来测量中子,这种测量方法采取的是转换靶+PIN+PIN的方式,转换靶一般为铀靶或聚乙烯靶:选择铀靶作转换靶,则存在PIN对中子的直照灵敏度要远大于裂变灵敏度的问题;选择聚乙烯靶作转换靶,则存在能谱响应不够平坦的问题。因此,现有技术中存在的中子探测器实际上并不能够精确地测量低强度脉冲中子源的中子总数。The compensation method neutron detector is to use the total signal current measured by PIN minus the n and γ direct light signal current measured by another PIN to measure neutrons. This measurement method adopts the method of switching target + PIN + PIN, switching The target is generally a uranium target or a polyethylene target: if the uranium target is selected as the conversion target, there is a problem that the direct irradiation sensitivity of PIN to neutrons is much greater than the fission sensitivity; if the polyethylene target is selected as the conversion target, the energy spectrum response is not flat enough The problem. Therefore, the neutron detectors existing in the prior art cannot actually accurately measure the total number of neutrons in the low-intensity pulsed neutron source.

发明内容Contents of the invention

本发明的目的在于提供一种核反应辐射转换靶及其制备方法和一种补偿型中子探测器,采用本发明提供的核反应辐射转换靶制备的补偿型中子探测器具有较平坦的能量响应、较高的中子灵敏度和n/γ分辨能力,为精确地测量低强度脉冲中子源的中子总数奠定了基础。The object of the present invention is to provide a nuclear reaction radiation conversion target and its preparation method and a compensating neutron detector. The compensating neutron detector prepared by using the nuclear reaction radiation conversion target provided by the present invention has relatively flat energy response, Higher neutron sensitivity and n/γ resolution capability lay the foundation for accurate measurement of the total number of neutrons in low-intensity pulsed neutron sources.

本发明提供了一种核反应辐射转换靶的制备方法,包括以下步骤:The invention provides a method for preparing a nuclear reaction radiation conversion target, comprising the following steps:

(1)对基片的表面进行预处理;(1) pretreating the surface of the substrate;

(2)将涂料涂覆在所述步骤(1)预处理后的基片表面,所述涂料包括固化剂、树脂、稀释剂和硼粉;(2) Coating is coated on the substrate surface after described step (1) pretreatment, and described coating comprises curing agent, resin, diluent and boron powder;

(3)将所述步骤(2)涂覆涂料后的基片进行烘干固化,得到核反应辐射转换靶。(3) drying and curing the substrate coated with the paint in the step (2) to obtain a nuclear reaction radiation conversion target.

优选的,步骤(2)所述涂料中固化剂、树脂、稀释剂和硼粉的质量比为1:(2~3):(5~7):(3~4)。Preferably, the mass ratio of curing agent, resin, diluent and boron powder in the coating in step (2) is 1: (2-3): (5-7): (3-4).

优选的,所述硼粉为无定形10B粉末。Preferably, the boron powder is amorphous 10 B powder.

优选的,所述硼粉在使用前进行预处理,所述预处理包括研磨、烘烤和二次研磨。Preferably, the boron powder is pretreated before use, and the pretreatment includes grinding, baking and secondary grinding.

优选的,所述预处理后硼粉的粒度小于1.0μm。Preferably, the particle size of the boron powder after the pretreatment is less than 1.0 μm.

优选的,步骤(3)中所述烘干固化包括干燥处理和烘烤处理。Preferably, the drying and curing in step (3) includes drying treatment and baking treatment.

优选的,所述烘烤处理采用梯度升温方式,起始温度为140~160℃,终点温度为440~460℃,每次升温幅度为40~60℃,每次升温后保温时间为8~12min。Preferably, the baking process adopts a gradient heating method, the initial temperature is 140-160°C, the end temperature is 440-460°C, the temperature increase range is 40-60°C each time, and the holding time after each temperature increase is 8-12min .

本发明提供了一种核反应辐射转换靶,包括基片和在所述基片表面的固化涂层,形成所述固化涂层的原料包括固化剂、树脂、稀释剂和硼粉。The invention provides a nuclear reaction radiation conversion target, which comprises a substrate and a cured coating on the surface of the substrate. The raw materials for forming the cured coating include curing agent, resin, diluent and boron powder.

优选的,所述固化涂层的厚度为8~10μm。Preferably, the thickness of the cured coating is 8-10 μm.

本发明提供了一种补偿型中子探测器,包括4He闪烁体、压力容器、光电倍增管、高压电源和记录传输信号设备,还包括位于所述压力容器入射窗外的聚乙烯核反冲辐射转换靶和位于所述压力容器入射窗内的核反应辐射转换靶,所述核反应辐射转换靶为上述技术方案所述的核反应辐射转换靶。The invention provides a compensated neutron detector, comprising 4 He scintillator, pressure vessel, photomultiplier tube, high-voltage power supply and equipment for recording and transmitting signals, and also includes polyethylene nuclear recoil radiation located outside the incident window of the pressure vessel A conversion target and a nuclear reaction radiation conversion target located in the incident window of the pressure vessel, the nuclear reaction radiation conversion target being the nuclear reaction radiation conversion target described in the above technical solution.

本发明提供了一种核反应辐射转换靶的制备方法,首先对基片的表面进行预处理;然后将涂料涂覆在预处理后的基片表面,所述涂料包括固化剂、树脂、稀释剂和硼粉;最后将所述涂覆涂料后的基片进行烘干固化,得到核反应辐射转换靶。本发明提供的制备方法可操作性强,通过简单的操作步骤即可制备得到均匀性好且性能稳定的核反应辐射转换靶。The invention provides a method for preparing a nuclear reaction radiation conversion target. Firstly, the surface of a substrate is pretreated; then a coating is coated on the surface of the pretreated substrate, and the coating includes a curing agent, a resin, a diluent and Boron powder; finally drying and curing the coated substrate to obtain a nuclear reaction radiation conversion target. The preparation method provided by the invention has strong operability, and the nuclear reaction radiation conversion target with good uniformity and stable performance can be prepared through simple operation steps.

本发明提供了一种核反应辐射转换靶包括基片和所述基片表面的固化涂层,形成所述固化涂层的原料包括固化剂、树脂、稀释剂和硼粉。本发明提供的核反应辐射转换靶能够在快中子能区实现能量响应补偿,应用于补偿型中子探测器中,有利于在中子总数测量过程中保持较平坦的能量响应、较高的中子灵敏度和n/γ分辨能力,为精确地测量低强度脉冲中子源的中子总数奠定了基础。理论计算和实验结果表明,包括本发明提供的核反应辐射转换靶的补偿型中子探测器,中子能量在1~15MeV区间时,其能量响应在1.01~1.44范围内,中子灵敏度为10-15C·cm,n/γ≥5。The invention provides a nuclear reaction radiation conversion target comprising a substrate and a cured coating on the surface of the substrate. The raw materials for forming the cured coating include curing agent, resin, diluent and boron powder. The nuclear reaction radiation conversion target provided by the present invention can realize energy response compensation in the fast neutron energy region, and is applied in a compensated neutron detector, which is conducive to maintaining relatively flat energy response and high neutron neutron total number measurement process. The neutron sensitivity and n/γ resolving power have laid the foundation for accurately measuring the total number of neutrons in low-intensity pulsed neutron sources. Theoretical calculations and experimental results show that the compensating neutron detector including the nuclear reaction radiation conversion target provided by the present invention, when the neutron energy is in the range of 1-15 MeV, its energy response is in the range of 1.01-1.44, and the neutron sensitivity is 10 - 15 C cm, n/γ≥5.

附图说明Description of drawings

下面结合附图和具体实施方式对本发明作进一步详细的说明。The present invention will be further described in detail below in conjunction with the accompanying drawings and specific embodiments.

图1为本发明实施例4提供的补偿型中子探测器的结构示意图。Fig. 1 is a schematic structural diagram of a compensation neutron detector provided by Embodiment 4 of the present invention.

具体实施方式detailed description

本发明提供了一种核反应辐射转换靶的制备方法,包括以下步骤:The invention provides a method for preparing a nuclear reaction radiation conversion target, comprising the following steps:

(1)对基片的表面进行预处理;(1) pretreating the surface of the substrate;

(2)将涂料涂覆在所述步骤(1)预处理后的基片表面,所述涂料包括固化剂、树脂、稀释剂和硼粉;(2) Coating is coated on the substrate surface after described step (1) pretreatment, and described coating comprises curing agent, resin, diluent and boron powder;

(3)将所述步骤(2)涂覆涂料后的基片进行烘干固化,得到核反应辐射转换靶。(3) drying and curing the substrate coated with the paint in the step (2) to obtain a nuclear reaction radiation conversion target.

本发明提供了一种核反应辐射转换靶的制备方法,首先对基片的表面进行预处理;然后将涂料涂覆在预处理后的基片表面,所述涂料包括固化剂、树脂、稀释剂和硼粉;最后将所述涂覆涂料后的基片进行烘干固化,得到核反应辐射转换靶。采用本发明提供的制备方法能够获得均匀性较好的核反应辐射转换靶,包括本发明提供的核反应辐射转换靶的补偿型中子探测器具有较平坦的能量响应、较高的中子灵敏度和n/γ分辨能力,为精确地测量低强度脉冲中子源的中子总数奠定了基础。The invention provides a method for preparing a nuclear reaction radiation conversion target. Firstly, the surface of a substrate is pretreated; then a coating is coated on the surface of the pretreated substrate, and the coating includes a curing agent, a resin, a diluent and Boron powder; finally drying and curing the coated substrate to obtain a nuclear reaction radiation conversion target. The preparation method provided by the present invention can obtain a nuclear reaction radiation conversion target with better uniformity, and the compensation type neutron detector comprising the nuclear reaction radiation conversion target provided by the present invention has relatively flat energy response, high neutron sensitivity and n The /γ resolution capability lays the foundation for accurately measuring the total number of neutrons in low-intensity pulsed neutron sources.

本发明对基片的表面进行预处理。在本发明中,所述基片的厚度优选为0.8~1.2mm。本发明对于所述基片的材质没有特殊的限定,采用本领域技术人员熟知的能够作为核反应辐射转换靶使用的基片的材料即可。本发明优选采用金属基片。在本发明的实施例中,具体采用铝片作为基片。本发明对于所述基片的形状没有特殊的要求,根据实际需要采用本领域技术人员熟知的基片的形状即可。在本发明的实施例中,具体采用圆形基片。在本发明中,所述对基片的表面进行预处理优选包括对基片的表面进行打磨抛光、清洗和烘干。The invention pretreats the surface of the substrate. In the present invention, the thickness of the substrate is preferably 0.8-1.2 mm. In the present invention, there is no special limitation on the material of the substrate, and the material of the substrate well known to those skilled in the art can be used as a nuclear reaction radiation conversion target. Metal substrates are preferred for the present invention. In the embodiment of the present invention, an aluminum sheet is specifically used as the substrate. The present invention has no special requirements on the shape of the substrate, and the shape of the substrate well known to those skilled in the art can be adopted according to actual needs. In the embodiment of the present invention, a circular substrate is specifically used. In the present invention, the pretreatment on the surface of the substrate preferably includes grinding and polishing, cleaning and drying the surface of the substrate.

本发明对于所述打磨抛光没有特殊的限定,采用本领域技术人员熟知的打磨抛光的技术方案即可。在本发明的实施例中,具体采用1200目砂纸对基片的表面进行打磨抛光,直至表面光滑、无毛刺。In the present invention, there is no special limitation on the grinding and polishing, and the technical solution of grinding and polishing well known to those skilled in the art can be adopted. In the embodiment of the present invention, specifically, 1200-grit sandpaper is used to grind and polish the surface of the substrate until the surface is smooth and free of burrs.

本发明优选对打磨抛光后的基片进行清洗。本发明对于所述清洗没有特殊的限定,采用本领域技术人员熟知的清洗的技术方案即可。本发明优选采用乙醇对打磨抛光后的基片进行清洗,以去除基片表面的灰尘、污渍。In the present invention, the ground and polished substrate is preferably cleaned. The present invention has no special limitation on the cleaning, and the technical solutions for cleaning well known to those skilled in the art can be adopted. In the present invention, ethanol is preferably used to clean the ground and polished substrate to remove dust and stains on the surface of the substrate.

本发明优选对清洗后的基片进行烘干。本发明对于所述烘干没有特殊的限定,采用本领域技术人员熟知的烘干的技术方案即可。本发明优选采用热风枪对清洗后的基片进行烘干,直至乙醇挥发完全。In the present invention, the washed substrate is preferably dried. The present invention has no special limitation on the drying, and the technical solution of drying well known to those skilled in the art can be adopted. In the present invention, a hot air gun is preferably used to dry the cleaned substrate until the ethanol is completely volatilized.

完成对基片的预处理后,本发明将涂料涂覆在所述预处理后的基片表面,所述涂料包括固化剂、树脂、稀释剂和硼粉。在本发明中,所述涂料中固化剂、树脂、稀释剂和硼粉的质量比优选为1:(2~3):(5~7):(3~4),更优选为1:2:6:3、1:2:6:4、1:3:6:3或1:3:6:4。After the pretreatment of the substrate is completed, the present invention coats the paint on the surface of the pretreated substrate, and the paint includes a curing agent, a resin, a diluent and boron powder. In the present invention, the mass ratio of curing agent, resin, diluent and boron powder in the coating is preferably 1: (2-3): (5-7): (3-4), more preferably 1:2 :6:3, 1:2:6:4, 1:3:6:3 or 1:3:6:4.

在本发明中,所述涂料包括固化剂、树脂、稀释剂和硼粉。在本发明中,所述硼粉优选为无定形10B粉末。天然硼由10B和11B两种稳定同位素组成,天然丰度分别为19.3%和80.7%。10B的热中子吸收截面约是11B的8万倍,天然丰度的硼对热中子的吸收截面仅为750b。在本发明中,为提高热中子与10B的反应截面,优选采用无定形10B粉末制备核反应辐射转换靶。在本发明中,所述无定形10B粉末的纯度优选﹥95.0%。In the present invention, the coating includes curing agent, resin, diluent and boron powder. In the present invention, the boron powder is preferably amorphous 10 B powder. Natural boron consists of two stable isotopes, 10 B and 11 B, with natural abundances of 19.3% and 80.7%, respectively. The thermal neutron absorption cross-section of 10 B is about 80,000 times that of 11 B, and the absorption cross-section of boron with natural abundance is only 750b for thermal neutrons. In the present invention, in order to increase the reaction cross section between thermal neutrons and 10 B, it is preferred to use amorphous 10 B powder to prepare the nuclear reaction radiation conversion target. In the present invention, the purity of the amorphous 10 B powder is preferably >95.0%.

在本发明中,所述硼粉在使用前优选进行预处理,所述预处理包括研磨、烘烤和二次研磨。本发明对于所述研磨没有特殊的限定,采用本领域技术人员熟知的研磨的技术方案即可。本发明优选采用球磨机对所述硼粉进行研磨。在本发明中,所述研磨时间优选为20~30h,更优选为24~28h。在本发明中,所述研磨后硼粉的粒度优选小于1.0μm。本发明优选采用扫描电镜测量研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉。In the present invention, the boron powder is preferably pretreated before use, and the pretreatment includes grinding, baking and secondary grinding. In the present invention, there is no special limitation on the grinding, and the technical solution of grinding known to those skilled in the art can be adopted. In the present invention, a ball mill is preferably used to grind the boron powder. In the present invention, the grinding time is preferably 20-30 hours, more preferably 24-28 hours. In the present invention, the particle size of the ground boron powder is preferably less than 1.0 μm. In the present invention, a scanning electron microscope is preferably used to measure the particle size of the ground boron powder, so as to ensure that boron powder with a particle size of less than 1.0 μm is obtained.

本发明优选对研磨后的硼粉进行烘烤。在本发明中,所述烘烤的温度优选为110~150℃,更优选为120~135℃;所述烘烤的时间优选为0.5~2h,更优选为1~1.5h。本发明对于所述烘烤所采用的设备没有特殊的限定,采用本领域技术人员熟知的用于烘烤的设备即可。本发明优选采用马弗炉对研磨后的硼粉进行烘烤。In the present invention, the ground boron powder is preferably baked. In the present invention, the baking temperature is preferably 110-150° C., more preferably 120-135° C.; the baking time is preferably 0.5-2 hours, more preferably 1-1.5 hours. In the present invention, there is no special limitation on the equipment used for the baking, and the equipment for baking well known to those skilled in the art can be used. In the present invention, a muffle furnace is preferably used to bake the ground boron powder.

本发明优选对烘烤后的硼粉进行二次研磨。本发明对于所述二次研磨没有特殊的限定,采用本领域技术人员熟知的研磨的技术方案即可。本发明优选采用球磨机对所述硼粉进行二次研磨。在本发明中,所述二次研磨时间优选为10~18h,更优选为12~15h。在本发明中,所述二次研磨后硼粉的粒度优选小于1.0μm。本发明优选采用扫描电镜测量二次研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉。In the present invention, the baked boron powder is preferably subjected to secondary grinding. In the present invention, there is no special limitation on the secondary grinding, and the technical solution of grinding well known to those skilled in the art can be adopted. In the present invention, a ball mill is preferably used to perform secondary grinding on the boron powder. In the present invention, the secondary grinding time is preferably 10-18 hours, more preferably 12-15 hours. In the present invention, the particle size of the boron powder after secondary grinding is preferably less than 1.0 μm. In the present invention, a scanning electron microscope is preferably used to measure the particle size of the boron powder after secondary grinding, so as to ensure that boron powder with a particle size of less than 1.0 μm is obtained.

将所述硼粉进行预处理后,本发明优选将预处理后的硼粉与固化剂、树脂、稀释剂混合,得到涂料。After the boron powder is pretreated, the present invention preferably mixes the pretreated boron powder with a curing agent, a resin, and a diluent to obtain a coating.

本发明对于所述固化剂没有特殊的限定,采用本领域技术人员熟知的固化剂即可。在本发明中,所述固化剂优选为胺类固化剂,更优选为乙二胺或二乙烯三胺。The present invention has no special limitation on the curing agent, and a curing agent well known to those skilled in the art can be used. In the present invention, the curing agent is preferably an amine curing agent, more preferably ethylenediamine or diethylenetriamine.

本发明对于所述树脂没有特殊的限定,采用本领域技术人员熟知的树脂即可。在本发明中,所述树脂优选为环氧树脂,更优选为#601环氧树脂、#604环氧树脂或#607环氧树脂。The present invention has no special limitation on the resin, and the resins well-known to those skilled in the art can be used. In the present invention, the resin is preferably epoxy resin, more preferably #601 epoxy resin, #604 epoxy resin or #607 epoxy resin.

本发明对于所述稀释剂没有特殊的限定,采用本领域技术人员熟知的稀释剂即可。在本发明中,所述稀释剂优选包括异辛基醚、环氧乙基苯或丁基缩水甘油醚。The present invention has no special limitation on the diluent, and a diluent well known to those skilled in the art can be used. In the present invention, the diluent preferably includes isooctyl ether, oxiranylbenzene or butyl glycidyl ether.

本发明对于所述将预处理后的硼粉与固化剂、树脂、稀释剂混合的方式没有特殊的限定,采用本领域技术人员熟知的混合的技术方案即可。本发明优选在超声条件下将预处理后的硼粉与固化剂、树脂、稀释剂混合。在本发明中,所述超声的时间优选为8~12min;所述超声的功率优选为18~22kHz。In the present invention, there is no special limitation on the method of mixing the pretreated boron powder with curing agent, resin, and diluent, and a mixing technical solution well known to those skilled in the art can be used. In the present invention, the pretreated boron powder is preferably mixed with curing agent, resin and diluent under ultrasonic conditions. In the present invention, the duration of the ultrasound is preferably 8-12 minutes; the power of the ultrasound is preferably 18-22 kHz.

得到涂料后,本发明将涂料涂覆在所述预处理后的基片表面。本发明对于所述涂覆的方式没有特殊的限定,采用本领域技术人员熟知的涂覆的技术方案即可。在本发明中,所述涂覆的方式优选为喷涂,具体可将涂料放入喷枪中,沿顺时针方向,同时保持喷射方向与所述预处理后的基片表面所在的平面夹角为28~32度,向所述预处理后的基片表面进行喷涂,在喷涂过程中旋转所述预处理后的基片或喷枪,以使喷涂均匀,避免造成涂料堆积而在后续处理中裂开。After the paint is obtained, the present invention coats the paint on the surface of the pretreated substrate. In the present invention, there is no special limitation on the coating method, and a coating technical solution well known to those skilled in the art can be used. In the present invention, the coating method is preferably spray coating. Specifically, the coating can be put into the spray gun in a clockwise direction, while keeping the angle between the spray direction and the plane where the pretreated substrate surface is located at 28° ~32 degrees, spraying on the surface of the pretreated substrate, rotating the pretreated substrate or the spray gun during the spraying process, so as to make the spraying even, and avoid the paint accumulation and cracking in the subsequent treatment.

完成所述涂覆后,本发明将所述涂覆涂料后的基片进行烘干固化,得到核反应辐射转换靶。在本发明中,所述烘干固化优选包括干燥处理和烘烤处理。After the coating is completed, the present invention dries and solidifies the coated substrate to obtain a nuclear reaction radiation conversion target. In the present invention, the drying curing preferably includes drying treatment and baking treatment.

本发明对于所述干燥处理没有特殊的限定,采用本领域技术人员熟知的能够将涂覆涂料后的基片表面进行干燥的技术方案即可。本发明优选采用热风枪进行所述干燥处理,具体是将热风枪的温度设定为100~250℃,热风枪喷嘴与涂覆涂料后的基片表面距离为5~10cm,进行1~3min的干燥处理。在本发明中,所述热风枪的温度优选为120~210℃,更优选为150~180℃。在本发明中,所述热风枪喷嘴与涂覆涂料后的基片表面距离优选为6~8cm。In the present invention, there is no special limitation on the drying treatment, and a technical solution known to those skilled in the art that can dry the surface of the coated substrate can be used. The present invention preferably adopts a heat gun to carry out the drying treatment, specifically, the temperature of the heat gun is set to 100-250° C., the distance between the nozzle of the heat gun and the surface of the coated substrate is 5-10 cm, and the drying process is carried out for 1-3 minutes. Dry processing. In the present invention, the temperature of the heat gun is preferably 120-210°C, more preferably 150-180°C. In the present invention, the distance between the nozzle of the heat gun and the surface of the coated substrate is preferably 6-8 cm.

完成所述干燥处理后,本发明优选对所述干燥处理后的涂覆有涂料的基片进行烘烤处理。在本发明中,所述烘烤处理优选采用梯度升温方式,防止温度突然升高,导致基片表面涂覆的涂料裂开。在本发明中,所述梯度升温方式中起始温度优选为140~160℃,更优选为145~155℃;终点温度优选为440~460℃,更优选为445~455℃;每次升温的幅度优选为40~60℃,更优选为45~55℃;每次升温后保温时间优选为8~12min,更优选为9~11min。本发明对于所述烘烤处理所采用的设备没有特殊的限定,采用本领域技术人员熟知的用于进行烘烤处理的设备即可。本发明优选采用马弗炉进行所述烘烤处理。After the drying treatment is completed, the present invention preferably performs baking treatment on the substrate coated with the coating after the drying treatment. In the present invention, the baking treatment preferably adopts a gradient temperature rise method to prevent the sudden rise in temperature from cracking the paint coated on the surface of the substrate. In the present invention, the initial temperature in the gradient heating method is preferably 140-160°C, more preferably 145-155°C; the end point temperature is preferably 440-460°C, more preferably 445-455°C; The range is preferably 40-60°C, more preferably 45-55°C; the holding time after each temperature rise is preferably 8-12 minutes, more preferably 9-11 minutes. In the present invention, there is no special limitation on the equipment used for the baking treatment, and the equipment for baking treatment well known to those skilled in the art can be used. In the present invention, a muffle furnace is preferably used for the baking treatment.

在实际应用中,可根据需要对含有单层固化涂层的核反应辐射转换靶继续进行多层涂覆,涂覆每一层需依次进行涂覆和烘干固化步骤,得到含有多层固化涂层的核反应辐射转换靶。In practical applications, the nuclear reaction radiation conversion target containing a single-layer cured coating can be continuously coated with multiple layers according to needs, and each layer needs to be coated and dried in sequence to obtain a multi-layer cured coating radiation conversion targets for nuclear reactions.

制备得到核反应辐射转换靶后,本发明优选将核反应辐射转换靶进行封装待用,为了不损坏核反应辐射转换靶的固化涂层,具体可将两块核反应辐射转换靶的固化涂层面相对放置,中间用塑料环隔开,然后用保鲜膜包好,并用胶带缠绕进行封装;所述塑料环厚度优选为8~12mm,外径与核反应辐射转换靶尺寸大小相当,内外径优选相差为6~10mm。After the nuclear reaction radiation conversion target is prepared, the present invention preferably packages the nuclear reaction radiation conversion target for use. In order not to damage the cured coating of the nuclear reaction radiation conversion target, specifically, the cured coating surfaces of two nuclear reaction radiation conversion targets can be placed opposite each other. The middle is separated by a plastic ring, then wrapped with plastic wrap, and wrapped with tape for packaging; the thickness of the plastic ring is preferably 8-12mm, the outer diameter is equivalent to the size of the nuclear reaction radiation conversion target, and the difference between the inner and outer diameters is preferably 6-10mm .

本发明提供了一种核反应辐射转换靶,包括基片和所述基片表面的固化涂层,形成所述固化涂层的原料包括固化剂、树脂、稀释剂和硼粉。在本发明中,所述固化涂层的厚度优选为8~10μm。在本发明中,所述固化涂层中硼粉含量优选为68%~78%。在本发明中,所述核反应辐射转换靶优选采用上述技术方案所述制备方法制备得到。The invention provides a nuclear reaction radiation conversion target, which comprises a substrate and a cured coating on the surface of the substrate. The raw materials for forming the cured coating include curing agent, resin, diluent and boron powder. In the present invention, the thickness of the cured coating is preferably 8-10 μm. In the present invention, the content of boron powder in the cured coating is preferably 68%-78%. In the present invention, the nuclear reaction radiation conversion target is preferably prepared by the preparation method described in the above technical solution.

在本发明中,所述核反应辐射转换靶的固化涂层厚度及固化涂层中硼粉含量均能够实现准确控制,所述固化涂层厚度和固化涂层中硼粉含量的测试方法具体包括以下步骤:In the present invention, the thickness of the cured coating of the nuclear reaction radiation conversion target and the content of boron powder in the cured coating can be accurately controlled, and the test methods for the thickness of the cured coating and the content of boron powder in the cured coating specifically include the following step:

(a)将涂料中固化剂、树脂和稀释剂分别进行烘烤处理,计算涂料中固化剂、树脂和稀释剂的质量剩余率,所述质量剩余率为所述烘烤处理前后质量差值与烘烤处理前的质量比;(a) curing agent, resin and diluent in the coating are respectively baked, and the mass residual rate of curing agent, resin and diluent in the calculation is calculated, and the mass residual rate is the difference between the mass difference before and after the baking treatment and The mass ratio before baking treatment;

(b)按涂料中固化剂、树脂、稀释剂和硼粉的质量比为b1:b2:b3:b4计,制备得到核反应辐射转换靶;(b) According to the mass ratio of curing agent, resin, diluent and boron powder in the coating as b1:b2 : b3: b4 , a nuclear reaction radiation conversion target is prepared ;

(c)按式I所示公式计算,得到固化涂层厚度;按式II所示公式计算,得到固化涂层中硼粉含量;(c) calculate by the formula shown in formula I, obtain cured coating thickness; Calculate by the formula shown in formula II, obtain the boron powder content in the cured coating;

其中,h为核反应辐射转换靶的固化涂层厚度,Among them, h is the cured coating thickness of the nuclear reaction radiation conversion target,

M为核反应辐射转换靶的质量,M is the mass of the nuclear reaction radiation conversion target,

m为预处理后的基片质量,m is the mass of the substrate after pretreatment,

a1、a2和a3分别为涂料中固化剂、树脂和稀释剂的质量剩余率,a 1 , a 2 and a 3 are the mass residual ratios of curing agent, resin and diluent in the paint respectively,

ρ为涂料中硼粉的密度,ρ is the density of boron powder in the paint,

s为预处理后的基片面积,s is the area of the substrate after pretreatment,

X为核反应辐射转换靶的固化涂层中硼粉含量。X is the boron powder content in the cured coating of the nuclear reaction radiation conversion target.

在本发明中,步骤(a)中将涂料中固化剂、树脂和稀释剂分别进行烘烤处理,计算涂料中固化剂、树脂和稀释剂的质量剩余率,所述质量剩余率为所述烘烤处理前后质量差值与烘烤处理前的质量比。在本发明中,所述烘烤处理优选将涂料中固化剂、树脂和稀释剂分别在230~250℃保温10~15min,在380~400℃保温10~15min,在430~450℃保温10~15min。In the present invention, in the step (a), the curing agent, resin and diluent in the coating are subjected to baking treatment respectively, and the mass residual rate of the curing agent, resin and diluent in the coating is calculated, and the mass residual rate is described in the baking process. The mass ratio before and after roasting treatment to the mass ratio before roasting treatment. In the present invention, the baking treatment is preferably to heat the curing agent, resin and diluent in the coating at 230-250°C for 10-15 minutes, at 380-400°C for 10-15 minutes, and at 430-450°C for 10-10 minutes. 15min.

本发明提供了一种补偿型中子探测器,包括4He闪烁体、压力容器、光电倍增管、高压电源和记录传输信号设备,还包括位于所述压力容器入射窗外的聚乙烯核反冲辐射转换靶和位于所述压力容器入射窗内的核反应辐射转换靶,所述核反应辐射转换靶为上述技术方案所述的核反应辐射转换靶。The invention provides a compensated neutron detector, comprising 4 He scintillator, pressure vessel, photomultiplier tube, high-voltage power supply and equipment for recording and transmitting signals, and also includes polyethylene nuclear recoil radiation located outside the incident window of the pressure vessel A conversion target and a nuclear reaction radiation conversion target located in the incident window of the pressure vessel, the nuclear reaction radiation conversion target being the nuclear reaction radiation conversion target described in the above technical solution.

本发明提供的补偿型中子探测器包括压力容器。本发明对于所述压力容器的材质没有特殊的限定,采用本领域技术人员熟知的能够用于制备压力容器的材料即可。本发明优选采用不锈钢材料制备压力容器,以保证压力容器内的压力能够维持稳定。本发明对于所述压力容器的形状没有特殊的要求,采用本领域技术人员熟知的压力容器的形状即可。本发明优选采用圆柱形压力容器,以实现最佳抗压效果。The compensation type neutron detector provided by the invention includes a pressure vessel. In the present invention, there is no special limitation on the material of the pressure vessel, and materials known to those skilled in the art that can be used to prepare the pressure vessel can be used. In the present invention, the pressure vessel is preferably made of stainless steel, so as to ensure that the pressure in the pressure vessel can be kept stable. The present invention has no special requirements on the shape of the pressure vessel, and the shape of the pressure vessel well known to those skilled in the art can be used. The present invention preferably adopts a cylindrical pressure vessel to achieve the best anti-pressure effect.

本发明提供的补偿型中子探测器包括置于压力容器内的4He闪烁体。在本发明中,所述4He的纯度优选≥99.99%。氦气(4He)是一种发光效率较高的气体闪烁体,且气体密度小,具有与γ射线作用截面小,γ射线的灵敏度较低,时间响应快等特点,在n/γ混合严重的低强度脉冲裂变中子测量中,选择4He作为闪烁体,有利于使补偿型中子探测器具有较高灵敏度和较好的n/γ分辨能力。The compensation type neutron detector provided by the present invention includes 4 He scintillator placed in a pressure vessel. In the present invention, the purity of the 4 He is preferably ≥99.99%. Helium ( 4 He ) is a gas scintillator with high luminous efficiency, and the gas density is small, it has the characteristics of small interaction cross section with γ-rays, low sensitivity of γ-rays, and fast time response. In the low-intensity pulse fission neutron measurement, 4 He is selected as the scintillator, which is beneficial to make the compensation neutron detector have higher sensitivity and better n/γ resolution ability.

本发明提供的补偿型中子探测器包括在压力容器入射窗外放置的聚乙烯核反冲辐射转换靶。本发明优选采用纯聚乙烯制备所述聚乙烯核反冲辐射转换靶。The compensation type neutron detector provided by the invention includes a polyethylene nuclear recoil radiation conversion target placed outside the incident window of a pressure vessel. In the present invention, pure polyethylene is preferably used to prepare the polyethylene nuclear recoil radiation conversion target.

本发明提供的补偿型中子探测器包括在压力容器入射窗内放置的核反应辐射转换靶。在本发明中,所述核反应辐射转换靶优选采用本发明上述技术方案提供的核反应辐射转换靶。The compensation type neutron detector provided by the invention includes a nuclear reaction radiation conversion target placed in the incident window of a pressure vessel. In the present invention, the nuclear reaction radiation conversion target preferably adopts the nuclear reaction radiation conversion target provided by the above technical solution of the present invention.

本发明提供的补偿型中子探测器包括压力容器出射窗外连接的光电倍增管。在本发明中,所述光电倍增管优选采用英国ET公司生产,型号为9215SB的光电倍增管,光谱范围为290~630nm,增益为106The compensation type neutron detector provided by the invention includes a photomultiplier tube connected outside the exit window of the pressure vessel. In the present invention, the photomultiplier tube is preferably a 9215SB photomultiplier tube manufactured by British ET Company, with a spectral range of 290-630 nm and a gain of 10 6 .

本发明提供的补偿型中子探测器包括与光电倍增管连接的记录传输信号设备。本发明对于所述记录传输信号设备没有特殊的要求,采用本领域技术人员熟知的记录传输信号设备即可。本发明优选采用电流计或示波器记录传输信号。The compensation type neutron detector provided by the invention includes a recording and transmission signal device connected with a photomultiplier tube. The present invention has no special requirements for the recording and transmission signal equipment, and the recording and transmission signal equipment well-known to those skilled in the art can be used. The present invention preferably uses a galvanometer or an oscilloscope to record the transmission signal.

本发明提供的补偿型中子探测器包括高压电源。本发明对于所述高压电源没有特殊的要求,采用本领域技术人员熟知的高压电源即可。在本发明中,所述高压电源的输出电压优选为±5~±50kV;所述高压电源的最大电流优选为5mA。本发明对于所述高压电源的连接方式没有特殊的要求,采用本领域技术人员熟知的高压电源的连接方式即可。本发明优选将所述高压电源与所述光电倍增管连接。The compensation type neutron detector provided by the invention includes a high voltage power supply. The present invention has no special requirements for the high-voltage power supply, and a high-voltage power supply well known to those skilled in the art can be used. In the present invention, the output voltage of the high-voltage power supply is preferably ±5˜±50 kV; the maximum current of the high-voltage power supply is preferably 5 mA. The present invention has no special requirements on the connection mode of the high-voltage power supply, and the connection mode of the high-voltage power supply well-known to those skilled in the art can be used. In the present invention, the high voltage power supply is preferably connected to the photomultiplier tube.

本发明提供的补偿型中子探测器测量低强度脉冲中子源的中子总数的原理是:在低强度脉冲中子辐射场中,中子束流入射本发明提供的补偿型中子探测器中,中子与聚乙烯核反冲辐射转换靶中的氢核和4He闪烁体中的氦核发生弹性散射产生反冲氢核和反冲氦核,将入射中子的一部分能量转移到反冲氢核和反冲氦核上;中子与核反应辐射转换靶中的10B发生核反应生成4He和7Li,将入射中子的一部分能量转移到反应产物4He和7Li上;核反应和核反冲产生的带电粒子将能量沉积到4He闪烁体中,激发4He发光,然后用光电倍增管收集光信号,并用电流计或示波器记录光电倍增管的输出信号,从而实现对中子的测量。本发明提供的补偿型中子探测器,1~15MeV能量响应在1.01~1.44范围内,中子灵敏度为10- 15C·cm,n/γ≥5,说明包括本发明提供的核反应辐射转换靶的补偿型中子探测器具有较平坦的能量响应、较高的中子灵敏度和n/γ分辨能力,为精确地测量低强度脉冲中子源的中子总数奠定了基础。The principle of the compensated neutron detector provided by the present invention to measure the total number of neutrons of the low-intensity pulsed neutron source is: in the low-intensity pulsed neutron radiation field, the neutron beam flows into the compensated neutron detector provided by the present invention In the process, the neutrons elastically scatter with the hydrogen nuclei in the polyethylene nuclear recoil radiation conversion target and the helium nuclei in the 4 He scintillator to produce recoil hydrogen nuclei and recoil helium nuclei, and transfer a part of the energy of the incident neutrons to the recoil Rush hydrogen nuclei and recoil helium nuclei; neutrons react with 10 B in the nuclear reaction radiation conversion target to generate 4 He and 7 Li, and transfer part of the energy of the incident neutrons to the reaction products 4 He and 7 Li; nuclear reactions and The charged particles generated by the nuclear recoil deposit energy into the 4He scintillator, excite 4He to emit light, then use the photomultiplier tube to collect the light signal, and use the current meter or oscilloscope to record the output signal of the photomultiplier tube, so as to realize the detection of neutrons. Measurement. The compensated neutron detector provided by the present invention has an energy response of 1 to 15 MeV in the range of 1.01 to 1.44, a neutron sensitivity of 10-15 C cm, and n/γ≥5, indicating that the nuclear reaction radiation conversion target provided by the present invention is included The compensated neutron detector has a relatively flat energy response, high neutron sensitivity and n/γ resolution, which lays the foundation for accurately measuring the total number of neutrons in low-intensity pulsed neutron sources.

下面将结合本发明中的实施例,对本发明中的技术方案进行清楚、完整地描述。显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本发明保护的范围。The technical solutions in the present invention will be clearly and completely described below in conjunction with the embodiments of the present invention. Apparently, the described embodiments are only some of the embodiments of the present invention, but not all of them. Based on the embodiments of the present invention, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts belong to the protection scope of the present invention.

实施例1:Example 1:

(1)以厚度为1mm、直径为50mm的圆形铝片为基片,采用1200目砂纸对铝基片的表面进行打磨抛光,直至表面光滑、无毛刺;然后采用乙醇对打磨抛光后的铝基片进行清洗,以去除表面的灰尘、污渍;然后采用热风枪对清洗后的基片进行烘干,直至乙醇挥发完全。(1) Take a circular aluminum sheet with a thickness of 1mm and a diameter of 50mm as the substrate, and use 1200 mesh sandpaper to polish the surface of the aluminum substrate until the surface is smooth and free of burrs; then use ethanol to polish the polished aluminum The substrate is cleaned to remove dust and stains on the surface; and then the cleaned substrate is dried with a heat gun until the ethanol is completely evaporated.

(2)采用球磨机将无定形10B粉末研磨20h,采用扫描电镜测量研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉,将所得粒度小于1.0μm的硼粉在马弗炉中于110℃烘烤2h,然后采用球磨机将烘烤处理后的硼粉二次研磨18h,采用扫描电镜测量二次研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉,将所得粒度小于1.0μm的硼粉与乙二胺、#601环氧树脂、异辛基醚混合,得到涂料;涂料中所述无定形10B粉末与乙二胺、#601环氧树脂、异辛基醚的质量比为3:1:2:5,所述混合在20kHz超声功率下超声8min。(2) Use a ball mill to grind the amorphous 10 B powder for 20 hours, and use a scanning electron microscope to measure the particle size of the ground boron powder to ensure that the boron powder with a particle size of less than 1.0 μm is obtained, and place the boron powder with a particle size of less than 1.0 μm in a muffle furnace Bake at 110°C for 2 hours, then use a ball mill to grind the baked boron powder for a second time for 18 hours, and use a scanning electron microscope to measure the particle size of the boron powder after the second grinding to ensure that the boron powder with a particle size of less than 1.0 μm is obtained, and the obtained particle size is less than 1.0 μm. The boron powder of μ m is mixed with ethylenediamine, #601 epoxy resin, and isooctyl ether to obtain a coating; the mass of amorphous 10 B powder, ethylenediamine, #601 epoxy resin, and isooctyl ether described in the coating The ratio was 3:1:2:5, and the mixture was sonicated for 8 min at 20 kHz ultrasonic power.

(3)将步骤(2)得到的涂料放入喷枪中,沿顺时针方向,同时保持喷射方向与步骤(1)预处理后的铝基片表面所在的平面夹角为30度,向所述预处理后的铝基片表面进行喷涂。(3) Put the coating obtained in step (2) into the spray gun, clockwise, while keeping the plane angle between the spray direction and the aluminum substrate surface after the step (1) pretreatment is 30 degrees, to the described The surface of the pretreated aluminum substrate is sprayed.

(4)将所述步骤(3)涂覆涂料后的铝基片进行烘干固化,得到核反应辐射转换靶;具体是采用热风枪将涂覆有涂料的铝基片进行干燥处理,所述热风枪的温度设定为100℃,热风枪喷嘴与涂覆涂料后的基片表面距离为5cm,干燥处理时间为3min;采用梯度升温方式将干燥处理后的涂覆有涂料的铝基片置于马弗炉中进行烘烤处理,所述梯度升温方式中起始温度为150℃,终点温度为450℃,每次升温幅度为50℃,每次升温后保温时间为10min。(4) drying and curing the aluminum substrate coated with the coating in the step (3) to obtain a nuclear reaction radiation conversion target; specifically, a heat gun is used to dry the coated aluminum substrate, and the hot air The gun temperature was set at 100°C, the distance between the hot air gun nozzle and the coated substrate surface was 5 cm, and the drying treatment time was 3 minutes; the dried coated aluminum substrate was placed in a Baking treatment was carried out in a muffle furnace. In the gradient heating method, the initial temperature was 150° C., the end temperature was 450° C., the temperature increase range was 50° C., and the holding time after each temperature increase was 10 minutes.

实施例2:Example 2:

(1)以厚度为0.8mm、直径为50mm的圆形铝片为基片,采用1200目砂纸对铝基片的表面进行打磨抛光,直至表面光滑、无毛刺;然后采用乙醇对打磨抛光后的铝基片进行清洗,以去除表面的灰尘、污渍;然后采用热风枪对清洗后的基片进行烘干,直至乙醇挥发完全。(1) Take a circular aluminum sheet with a thickness of 0.8mm and a diameter of 50mm as the substrate, and use 1200 mesh sandpaper to polish the surface of the aluminum substrate until the surface is smooth and free of burrs; then use ethanol to polish the surface of the aluminum substrate. Clean the aluminum substrate to remove dust and stains on the surface; then use a heat gun to dry the cleaned substrate until the ethanol is completely evaporated.

(2)采用球磨机将无定形10B粉末研磨30h,采用扫描电镜测量研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉,将所得粒度小于1.0μm的硼粉在马弗炉中于150℃烘烤0.5h,然后采用球磨机将烘烤处理后的硼粉二次研磨10h,采用扫描电镜测量二次研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉,将所得粒度小于1.0μm的硼粉与二乙烯三胺、#604环氧树脂、环氧乙基苯混合,得到涂料;涂料中所述无定形10B粉末与二乙烯三胺、#604环氧树脂、环氧乙基苯的质量比为4:1:3:7,所述混合在22kHz超声功率下超声10min。(2) Use a ball mill to grind the amorphous 10 B powder for 30 hours, and use a scanning electron microscope to measure the particle size of the ground boron powder to ensure that the boron powder with a particle size of less than 1.0 μm is obtained, and place the boron powder with a particle size of less than 1.0 μm in a muffle furnace Bake at 150°C for 0.5h, then use a ball mill to grind the baked boron powder for a second time for 10h, use a scanning electron microscope to measure the particle size of the boron powder after the second grinding, to ensure that the boron powder with a particle size of less than 1.0μm is obtained, and the obtained particle size is less than The boron powder of 1.0 μ m is mixed with diethylenetriamine, #604 epoxy resin, epoxyethylbenzene to obtain a coating; the amorphous 10 B powder described in the coating is mixed with diethylenetriamine, #604 epoxy resin, epoxy The mass ratio of ethylbenzene is 4:1:3:7, and the mixture is sonicated at 22 kHz ultrasonic power for 10 min.

(3)将步骤(2)得到的涂料放入喷枪中,沿顺时针方向,同时保持喷射方向与步骤(1)预处理后的铝基片表面所在的平面夹角为30度,向所述预处理后的铝基片表面进行喷涂。(3) Put the coating that step (2) obtains into the spray gun, along the clockwise direction, while keeping the plane angle between the spray direction and the aluminum substrate surface after the step (1) pretreatment is 30 degrees, to the described The surface of the pretreated aluminum substrate is sprayed.

(4)将所述步骤(3)涂覆涂料后的铝基片进行烘干固化,得到核反应辐射转换靶;具体是采用热风枪将涂覆有涂料的铝基片进行干燥处理,所述热风枪的温度设定为250℃,热风枪喷嘴与涂覆涂料后的基片表面距离为10cm,干燥处理时间为1min;采用梯度升温方式将干燥处理后的涂覆有涂料的铝基片置于马弗炉中进行烘烤处理,所述梯度升温方式中起始温度为150℃,终点温度为450℃,每次升温幅度为50℃,每次升温后保温时间为8min。(4) drying and curing the aluminum substrate coated with the coating in the step (3) to obtain a nuclear reaction radiation conversion target; specifically, a heat gun is used to dry the coated aluminum substrate, and the hot air The temperature of the gun was set at 250°C, the distance between the hot air gun nozzle and the coated substrate surface was 10 cm, and the drying treatment time was 1 min; the dried coated aluminum substrate was placed in a Baking treatment was carried out in a muffle furnace. In the gradient heating method, the initial temperature was 150° C., the end temperature was 450° C., the temperature increase range was 50° C., and the holding time after each temperature increase was 8 minutes.

实施例3:Example 3:

(1)以厚度为1.2mm、直径为50mm的圆形铝片为基片,采用1200目砂纸对铝基片的表面进行打磨抛光,直至表面光滑、无毛刺;然后采用乙醇对打磨抛光后的铝基片进行清洗,以去除表面的灰尘、污渍;然后采用热风枪对清洗后的基片进行烘干,直至乙醇挥发完全。(1) Take a circular aluminum sheet with a thickness of 1.2mm and a diameter of 50mm as the substrate, and use 1200 mesh sandpaper to polish the surface of the aluminum substrate until the surface is smooth and free of burrs; then use ethanol to polish the surface of the aluminum substrate. Clean the aluminum substrate to remove dust and stains on the surface; then use a heat gun to dry the cleaned substrate until the ethanol is completely evaporated.

(2)采用球磨机将无定形10B粉末研磨25h,采用扫描电镜测量研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉,将所得粒度小于1.0μm的硼粉在马弗炉中于120℃烘烤1.5h,然后采用球磨机将烘烤处理后的硼粉二次研磨14h,采用扫描电镜测量二次研磨后硼粉的粒度,保证得到粒度小于1.0μm的硼粉,将所得粒度小于1.0μm的硼粉与二乙烯三胺、#607环氧树脂、丁基缩水甘油醚混合,得到涂料;涂料中所述无定形10B粉末与二乙烯三胺、#607环氧树脂、丁基缩水甘油醚的质量比为4:1:2:6,所述混合在18kHz超声功率下超声12min。(2) Use a ball mill to grind the amorphous 10 B powder for 25 hours, and use a scanning electron microscope to measure the particle size of the ground boron powder to ensure that the boron powder with a particle size of less than 1.0 μm is obtained, and place the boron powder with a particle size of less than 1.0 μm in a muffle furnace Bake at 120°C for 1.5h, then use a ball mill to grind the baked boron powder for a second time for 14h, use a scanning electron microscope to measure the particle size of the boron powder after the second grinding, to ensure that the boron powder with a particle size of less than 1.0μm is obtained, and the obtained particle size is less than The boron powder of 1.0 μ m is mixed with diethylenetriamine, #607 epoxy resin, butyl glycidyl ether to obtain a coating; the amorphous 10 B powder in the coating is mixed with diethylenetriamine, #607 epoxy resin, butyl The mass ratio of glycidyl ether was 4:1:2:6, and the mixture was sonicated for 12 min at 18 kHz ultrasonic power.

(3)将步骤(2)得到的涂料放入喷枪中,沿顺时针方向,同时保持喷射方向与步骤(1)预处理后的铝基片表面所在的平面夹角为30度,向所述预处理后的铝基片表面进行喷涂。(3) Put the coating that step (2) obtains into the spray gun, along the clockwise direction, while keeping the plane angle between the spray direction and the aluminum substrate surface after the step (1) pretreatment is 30 degrees, to the described The surface of the pretreated aluminum substrate is sprayed.

(4)将所述步骤(3)涂覆涂料后的铝基片进行烘干固化,得到核反应辐射转换靶;具体是采用热风枪将涂覆有涂料的铝基片进行干燥处理,所述热风枪的温度设定为160℃,热风枪喷嘴与涂覆涂料后的基片表面距离为8cm,干燥处理时间为2min;采用梯度升温方式将干燥处理后的涂覆有涂料的铝基片置于马弗炉中进行烘烤处理,所述梯度升温方式中起始温度为150℃,终点温度为450℃,每次升温幅度为50℃,每次升温后保温时间为12min。(4) drying and curing the aluminum substrate coated with the coating in the step (3) to obtain a nuclear reaction radiation conversion target; specifically, a heat gun is used to dry the coated aluminum substrate, and the hot air The temperature of the gun was set at 160°C, the distance between the hot air gun nozzle and the coated substrate surface was 8 cm, and the drying treatment time was 2 min; the dried coated aluminum substrate was placed in a Baking treatment was carried out in a muffle furnace. In the gradient heating method, the initial temperature was 150° C., the end temperature was 450° C., the temperature increase range was 50° C., and the holding time after each temperature increase was 12 minutes.

实施例4Example 4

采用实施例1制备得到的核反应辐射转换靶制备补偿型中子探测器,所述补偿型中子探测器包括4He闪烁体、压力容器、聚乙烯核反冲辐射转换靶、核反应辐射转换靶、光电倍增管、高压电源和记录传输信号设备,结构如图1所示。Using the nuclear reaction radiation conversion target prepared in Example 1 to prepare a compensation type neutron detector, the compensation type neutron detector includes He scintillator, pressure vessel, polyethylene nuclear recoil radiation conversion target, nuclear reaction radiation conversion target, The structure of the photomultiplier tube, high voltage power supply and recording and transmission signal equipment is shown in Figure 1.

采用蒙卡程序MCNPX基于本发明提供的补偿型中子探测器结构建立理论计算模型,针对不同能量的中子进行能量响应模拟计算。计算结果表明,本发明提供的补偿型中子探测器在中子能量为1~15MeV时,能量响应在1.01~1.44范围内。The Monte Cal program MCNPX is used to establish a theoretical calculation model based on the compensated neutron detector structure provided by the present invention, and perform energy response simulation calculations for neutrons of different energies. The calculation results show that the compensation type neutron detector provided by the invention has an energy response in the range of 1.01-1.44 when the neutron energy is 1-15 MeV.

利用西安脉冲反应堆径向孔道和热柱孔道对本发明提供的补偿型中子探测器进行中子灵敏度测试实验,在反应堆稳态功率2MW的条件下,本发明提供的补偿型中子探测器的中子灵敏度为10-15C·cm。The compensation type neutron detector provided by the present invention is tested for neutron sensitivity by using radial channels and thermal column channels of the Xi’an pulse reactor. The sub-sensitivity is 10 -15 C·cm.

利用钴源、铯源测试本发明提供的补偿型中子探测器的γ灵敏度,结果表明本发明提供的补偿型中子探测器的n/γ≥5。The gamma sensitivity of the compensated neutron detector provided by the invention is tested by cobalt source and cesium source, and the result shows that n/γ≥5 of the compensated neutron detector provided by the invention.

由以上实施例可以看出,采用本发明提供的制备方法能够获得均匀性较好的核反应辐射转换靶,包括本发明提供的核反应辐射转换靶的补偿型中子探测器具有较平坦的能量响应、较高的中子灵敏度和n/γ分辨能力,为精确地测量低强度脉冲中子源的中子总数奠定了基础。It can be seen from the above examples that the preparation method provided by the present invention can obtain a nuclear reaction radiation conversion target with better uniformity, and the compensating neutron detector comprising the nuclear reaction radiation conversion target provided by the present invention has a relatively flat energy response, Higher neutron sensitivity and n/γ resolution capability lay the foundation for accurate measurement of the total number of neutrons in low-intensity pulsed neutron sources.

以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。The above is only a preferred embodiment of the present invention, it should be pointed out that, for those of ordinary skill in the art, without departing from the principle of the present invention, some improvements and modifications can also be made, and these improvements and modifications can also be made. It should be regarded as the protection scope of the present invention.

Claims (10)

1.一种核反应辐射转换靶的制备方法,包括以下步骤:1. A preparation method for a nuclear reaction radiation conversion target, comprising the following steps: (1)对基片的表面进行预处理;(1) pretreating the surface of the substrate; (2)将涂料涂覆在所述步骤(1)预处理后的基片表面,所述涂料包括固化剂、树脂、稀释剂和硼粉;(2) Coating is coated on the substrate surface after described step (1) pretreatment, and described coating comprises curing agent, resin, diluent and boron powder; (3)将所述步骤(2)涂覆涂料后的基片进行烘干固化,得到核反应辐射转换靶。(3) drying and curing the substrate coated with the paint in the step (2) to obtain a nuclear reaction radiation conversion target. 2.根据权利要求1所述的制备方法,其特征在于,步骤(2)所述涂料中固化剂、树脂、稀释剂和硼粉的质量比为1:(2~3):(5~7):(3~4)。2. The preparation method according to claim 1, characterized in that, the mass ratio of curing agent, resin, diluent and boron powder in the coating of step (2) is 1: (2~3): (5~7 ): (3~4). 3.根据权利要求1或2所述的制备方法,其特征在于,所述硼粉为无定形10B粉末。3. The preparation method according to claim 1 or 2, characterized in that, the boron powder is an amorphous 10 B powder. 4.根据权利要求3所述的制备方法,其特征在于,所述硼粉在使用前进行预处理,所述预处理包括研磨、烘烤和二次研磨。4. The preparation method according to claim 3, wherein the boron powder is pretreated before use, and the pretreatment includes grinding, baking and secondary grinding. 5.根据权利要求4所述的制备方法,其特征在于,所述预处理后硼粉的粒度小于1.0μm。5. The preparation method according to claim 4, characterized in that the particle size of the boron powder after the pretreatment is less than 1.0 μm. 6.根据权利要求1所述的制备方法,其特征在于,步骤(3)中所述烘干固化包括干燥处理和烘烤处理。6 . The preparation method according to claim 1 , wherein the drying and curing in step (3) includes drying treatment and baking treatment. 7 . 7.根据权利要求6所述的制备方法,其特征在于,所述烘烤处理采用梯度升温方式,起始温度为140~160℃,终点温度为440~460℃,每次升温幅度为40~60℃,每次升温后保温时间为8~12min。7. The preparation method according to claim 6, characterized in that, the baking process adopts a gradient heating method, the initial temperature is 140-160°C, the end temperature is 440-460°C, and the heating range is 40-40°C each time. 60°C, the holding time after each temperature rise is 8-12 minutes. 8.一种核反应辐射转换靶,其特征在于,包括基片和所述基片表面的固化涂层,形成所述固化涂层的原料包括固化剂、树脂、稀释剂和硼粉。8. A nuclear reaction radiation conversion target, characterized in that it comprises a substrate and a cured coating on the surface of the substrate, and the raw materials for forming the cured coating include curing agent, resin, diluent and boron powder. 9.根据权利要求8所述的核反应辐射转换靶,其特征在于,所述固化涂层的厚度为8~10μm。9. The nuclear reaction radiation conversion target according to claim 8, characterized in that the thickness of the cured coating is 8-10 μm. 10.一种补偿型中子探测器,包括4He闪烁体、压力容器、光电倍增管、高压电源和记录传输信号设备,其特征在于,还包括位于所述压力容器入射窗外的聚乙烯核反冲辐射转换靶和位于所述压力容器入射窗内的核反应辐射转换靶,所述核反应辐射转换靶为权利要求8或9所述的核反应辐射转换靶。10. A compensated neutron detector, comprising 4 He scintillator, pressure vessel, photomultiplier tube, high-voltage power supply and recording and transmission signal equipment, characterized in that it also includes a polyethylene nuclear reactor positioned outside the incident window of the pressure vessel An impact radiation conversion target and a nuclear reaction radiation conversion target located in the incident window of the pressure vessel, the nuclear reaction radiation conversion target being the nuclear reaction radiation conversion target described in claim 8 or 9.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110467865A (en) * 2018-05-09 2019-11-19 同方威视技术股份有限公司 A kind of painting boron method
CN114236600A (en) * 2021-11-25 2022-03-25 西北核技术研究所 A neutron beam monitoring system based on silicon carbide detector

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102628954A (en) * 2012-03-29 2012-08-08 西北核技术研究所 Neutron detector based on polyethylene combined gas scintillator
CN202404247U (en) * 2011-12-28 2012-08-29 同方威视技术股份有限公司 Fast neutron detector
CN202854343U (en) * 2012-06-21 2013-04-03 同方威视技术股份有限公司 Boracic gas film fast neutron detector
CN103995280A (en) * 2014-05-09 2014-08-20 南京航空航天大学 Boron film cathode of neutron detector and preparing method thereof
US20140374606A1 (en) * 2013-06-24 2014-12-25 Arktis Radiation Detectors Ltd. Detector Arrangement for the Detection of Ionizing Radiation and Method for Operating Such a Detector Arrangement
CN105137473A (en) * 2015-07-21 2015-12-09 时天成 Production method for boron-10 element used for neutron detector

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN202404247U (en) * 2011-12-28 2012-08-29 同方威视技术股份有限公司 Fast neutron detector
CN102628954A (en) * 2012-03-29 2012-08-08 西北核技术研究所 Neutron detector based on polyethylene combined gas scintillator
CN202854343U (en) * 2012-06-21 2013-04-03 同方威视技术股份有限公司 Boracic gas film fast neutron detector
US20140374606A1 (en) * 2013-06-24 2014-12-25 Arktis Radiation Detectors Ltd. Detector Arrangement for the Detection of Ionizing Radiation and Method for Operating Such a Detector Arrangement
CN103995280A (en) * 2014-05-09 2014-08-20 南京航空航天大学 Boron film cathode of neutron detector and preparing method thereof
CN105137473A (en) * 2015-07-21 2015-12-09 时天成 Production method for boron-10 element used for neutron detector

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110467865A (en) * 2018-05-09 2019-11-19 同方威视技术股份有限公司 A kind of painting boron method
US11090686B2 (en) 2018-05-09 2021-08-17 Nuctech Company Limited Method for coating boron
CN114236600A (en) * 2021-11-25 2022-03-25 西北核技术研究所 A neutron beam monitoring system based on silicon carbide detector

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