JPH07125739A - Sample container - Google Patents
Sample containerInfo
- Publication number
- JPH07125739A JPH07125739A JP24348594A JP24348594A JPH07125739A JP H07125739 A JPH07125739 A JP H07125739A JP 24348594 A JP24348594 A JP 24348594A JP 24348594 A JP24348594 A JP 24348594A JP H07125739 A JPH07125739 A JP H07125739A
- Authority
- JP
- Japan
- Prior art keywords
- sample container
- resin
- sample
- contact
- inorganic filler
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 229920005989 resin Polymers 0.000 claims abstract description 62
- 239000011347 resin Substances 0.000 claims abstract description 62
- 239000011256 inorganic filler Substances 0.000 claims abstract description 27
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 27
- 238000000034 method Methods 0.000 claims abstract description 14
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims abstract description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 5
- 229910052802 copper Inorganic materials 0.000 claims abstract description 3
- 239000010949 copper Substances 0.000 claims abstract description 3
- 239000002131 composite material Substances 0.000 claims description 9
- 239000000470 constituent Substances 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052582 BN Inorganic materials 0.000 claims description 4
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical group N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- 239000011888 foil Substances 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 claims description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 2
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims description 2
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 229910003460 diamond Inorganic materials 0.000 claims description 2
- 239000010432 diamond Substances 0.000 claims description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052737 gold Inorganic materials 0.000 claims description 2
- 239000010931 gold Substances 0.000 claims description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 2
- 239000000395 magnesium oxide Substances 0.000 claims description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 2
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 2
- 229910052709 silver Inorganic materials 0.000 claims description 2
- 239000004332 silver Substances 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000000945 filler Substances 0.000 abstract description 16
- -1 polypropylene Polymers 0.000 abstract description 8
- 239000004743 Polypropylene Substances 0.000 abstract description 7
- 229920001155 polypropylene Polymers 0.000 abstract description 7
- 238000001879 gelation Methods 0.000 abstract description 6
- 229910010272 inorganic material Inorganic materials 0.000 abstract description 5
- 239000011147 inorganic material Substances 0.000 abstract description 5
- 238000001816 cooling Methods 0.000 abstract description 4
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 229920002050 silicone resin Polymers 0.000 abstract description 4
- 238000000071 blow moulding Methods 0.000 abstract description 3
- 239000002904 solvent Substances 0.000 abstract description 2
- 238000003756 stirring Methods 0.000 abstract description 2
- 229920002472 Starch Polymers 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 239000008107 starch Substances 0.000 abstract 1
- 235000019698 starch Nutrition 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000003814 drug Substances 0.000 description 2
- 230000005489 elastic deformation Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
Classifications
-
- 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
- Y02W90/00—Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
- Y02W90/10—Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics
Landscapes
- Containers Having Bodies Formed In One Piece (AREA)
- Packging For Living Organisms, Food Or Medicinal Products That Are Sensitive To Environmental Conditiond (AREA)
- Packages (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、医学、化学、生物工学
の分野向けの熱プロセスを加える事を必要とするサンプ
ルを保持する容器の構造に関する。FIELD OF THE INVENTION The present invention relates to the construction of a container for holding a sample requiring the application of thermal processes for the fields of medicine, chemistry and biotechnology.
【0002】[0002]
【従来の技術】従来のサンプル容器では、厚い単体の樹
脂層だけで構成されていた。そのために温度プロセスを
外部より加えた場合に非常に熱伝達が悪く、効率よく加
熱冷却を容器内のサンプルに伝える事ができなかった。
またサンプル容器の外部表面のサンプル容器保持体と接
する部分の柔軟性が考慮されておらずサンプル容器保持
体との密着が不十分でサンプル容器保持体からサンプル
容器への熱伝達効率が悪かった。2. Description of the Related Art In a conventional sample container, it is composed of only a thick resin layer. Therefore, when the temperature process was applied from the outside, heat transfer was very poor, and heating / cooling could not be efficiently transferred to the sample in the container.
Further, the flexibility of the portion of the outer surface of the sample container that comes into contact with the sample container holder was not taken into consideration, and the close contact with the sample container holder was insufficient, resulting in poor heat transfer efficiency from the sample container holder to the sample container.
【0003】[0003]
【発明が解決しようとする課題】本発明は、このような
従来の欠点を解決して、温度プロセスを加える必要のあ
るサンプルに、外部からの加熱冷却を効率よくサンプル
に伝えるために成されたものである。SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned drawbacks of the prior art and to efficiently transfer the heating and cooling from the outside to the sample that needs to be subjected to a temperature process. It is a thing.
【0004】[0004]
【課題を解決するための手段】上記の課題を解決するた
めに成された本発明は、樹脂中に、熱伝導率が単体で1
0W/(mK)以上である無機材料を充填材として入れ
る事により、熱伝導を良好にすると言う技術的手段を採
用した。すなわち本来熱伝導率の小さい樹脂の欠点を樹
脂に分散された熱伝導率の大きい無機材料の充填材によ
り補完するということである。無機充填材の体積含有率
は低いと十分な熱伝導率向上の効果はなく少なくとも無
機充填材の体積含有率30%は必要である。無機充填材
の体積含有率が多ければ多いほど熱伝導率はよくなる。
無機充填材の体積含有率を多くすることは、特に90%
を越える場合には難しくなる。例えば真球の無機充填材
粒子を使用するといった手法を利用すれば充填材の体積
含有率は95%までは可能である。よって強度、熱伝導
率、コスト、形状等を考慮して無機充填材の体積含有率
30%から95%の範囲から自由に選べばよい。またこ
こで無機材料を充填材の形状は粒子及びウィスカー及び
繊維及び箔等から目的に合わせて自由に選べばよい。必
要であれば複数の形状を組み合わせてもよい。無機材料
の材質は窒化ボロン、酸化アルミニウム、炭化ケイ素、
窒化ケイ素、炭酸カルシウム、酸化マグネシウム、酸化
ケイ素、石英ガラス、酸化ジルコニウム、窒化チタン、
酸化ベリリウム、カーボン、ダイヤモンド、金、銀、
銅、アルミニウム、タングステン、モリブデン等が考え
られる。強度、絶縁性等を考慮し前記材料より目的に合
わせて自由に選べばよく必要であれば複数の材料を組み
合わせてもよい。SUMMARY OF THE INVENTION The present invention, which was made to solve the above-mentioned problems, has a resin having a single thermal conductivity of 1%.
The technical means of improving the heat conduction by incorporating an inorganic material of 0 W / (mK) or more as a filler was adopted. That is, the defect of the resin having originally low thermal conductivity is complemented by the filler of the inorganic material having high thermal conductivity dispersed in the resin. If the volume content of the inorganic filler is low, there is no sufficient effect of improving the thermal conductivity, and the volume content of the inorganic filler is at least 30%. The higher the volume content of the inorganic filler, the better the thermal conductivity.
Increasing the volume content of the inorganic filler is especially 90%
It will be difficult if it exceeds. For example, the volume content of the filler can be up to 95% by using a method of using spherical inorganic filler particles. Therefore, the volume content of the inorganic filler may be freely selected from the range of 30% to 95% in consideration of strength, thermal conductivity, cost, shape and the like. Further, here, the shape of the inorganic material filler may be freely selected from particles, whiskers, fibers, foils and the like according to the purpose. If necessary, a plurality of shapes may be combined. Inorganic materials are boron nitride, aluminum oxide, silicon carbide,
Silicon nitride, calcium carbonate, magnesium oxide, silicon oxide, quartz glass, zirconium oxide, titanium nitride,
Beryllium oxide, carbon, diamond, gold, silver,
Copper, aluminum, tungsten, molybdenum, etc. are considered. A material may be freely selected from the above materials in consideration of strength, insulating properties, etc. according to the purpose, and a plurality of materials may be combined if necessary.
【0005】サンプルに接する部分はサンプルの性質上
から無機充填材と接触することを避けて樹脂でなければ
ならない場合がある。そこでこの部分はサンプルの性質
により樹脂の種類を選び樹脂のみの部分を形成すればよ
い。ただしサンプルに接する樹脂のみで構成される部分
の厚さはあまり薄いと樹脂のみの層が破損等のためサン
プルが無機充填材と接触する可能性があるため樹脂の材
質にもよるが少なくとも5μmは必要である。一方厚さ
が一定以上ある場合には樹脂のみの部分の熱抵抗が大き
くなってしまいサンプルへの熱伝導が悪くなるため20
0μm以下が望ましい。すなわちサンプルに接する部分
は、樹脂のみで構成され、残部は樹脂と無機充填材の複
合体から構成された2つの部分から成ると言う技術的手
段を採用した。Due to the nature of the sample, the part in contact with the sample may have to be a resin so as to avoid contact with the inorganic filler. Therefore, for this portion, the type of resin may be selected according to the properties of the sample to form the portion of only resin. However, if the thickness of the part that is in contact with the sample and is composed only of resin is too thin, the sample may contact the inorganic filler due to damage of the resin-only layer, but depending on the resin material, at least 5 μm is necessary. On the other hand, if the thickness is more than a certain value, the thermal resistance of the resin-only part increases and the heat conduction to the sample deteriorates.
It is preferably 0 μm or less. That is, a technical means was adopted in which the portion in contact with the sample was composed only of the resin, and the remaining portion was composed of two portions composed of a composite of the resin and the inorganic filler.
【0006】サンプル容器の外部表面のサンプル容器保
持体と接する部分の構成成分樹脂がサンプル容器の主体
成分樹脂より柔軟な樹脂を使用することによりサンプル
容器保持体とあるサンプル容器の外部表面を密着させる
ことが可能となる。すなわちサンプル容器保持体のサン
プル容器を挿入する部分の穴の表面の凹凸部に柔軟な樹
脂が変形することにより密着しサンプル容器保持体から
サンプル容器に効率的に熱伝達が行われる。ここで柔軟
な樹脂の変形機構は塑性変形でも弾性変形でもよい。塑
性変形の場合好ましくはサンプル容器の外部表面のサン
プル容器保持体と接する部分の構成成分樹脂の引っ張り
強度が32MPa以下がよい。弾性変形の場合は好まし
くはサンプル容器の外部表面のサンプル容器保持体と接
する部分の構成成分樹脂の縦弾性率が1.4GPa以下
であるとよい。また柔軟な樹脂がゲル状樹脂という構成
でもよい。他の方法としてサンプルに加える温度プロセ
スが50℃以上100℃以下の範囲で行われる場合サン
プル容器の外部表面のサンプル容器保持体と接する部分
の構成成分樹脂の軟化温度が50℃であればサンプル容
器保持体と接する部分の構成成分樹脂が50℃以上の温
度プロセスのため熱により変形容易となり密着する。バ
イオテクノロジーの分野では印加温度プロセスの範囲は
ほとんど100℃以下である。よってサンプル容器の外
部表面のサンプル容器保持体と接する部分の構成成分樹
脂の軟化温度が100℃以下の樹脂から目的に応じた樹
脂を選べばよい。この柔軟な樹脂を使用する場合におい
ても無機充填材の体積含有率は30%以上95%以下の
範囲が好ましい。By using a resin whose constituent resin on the outer surface of the sample container in contact with the sample container holder is softer than the main component resin of the sample container, the sample container holder and the outer surface of a sample container are brought into close contact with each other. It becomes possible. That is, when the flexible resin is deformed, the flexible resin is brought into close contact with the irregularities on the surface of the hole of the sample container holder into which the sample container is inserted, and heat is efficiently transferred from the sample container holder to the sample container. The flexible resin deformation mechanism may be plastic deformation or elastic deformation. In the case of plastic deformation, the tensile strength of the constituent resin of the portion of the outer surface of the sample container that contacts the sample container holder is preferably 32 MPa or less. In the case of elastic deformation, it is preferable that the longitudinal elastic modulus of the constituent resin of the portion of the outer surface of the sample container which is in contact with the sample container holder is 1.4 GPa or less. Alternatively, the soft resin may be a gel resin. As another method, when the temperature process applied to the sample is performed in the range of 50 ° C. or higher and 100 ° C. or lower, if the softening temperature of the component resin on the outer surface of the sample container that contacts the sample container holder is 50 ° C. Due to the temperature process of 50 ° C. or higher, the component resin in the portion in contact with the holder is easily deformed by heat and adheres closely. In the field of biotechnology, the range of applied temperature process is almost 100 ° C. or less. Therefore, the resin suitable for the purpose may be selected from the resins having a softening temperature of 100 ° C. or less of the constituent resin of the portion of the outer surface of the sample container that contacts the sample container holder. Even when this soft resin is used, the volume content of the inorganic filler is preferably in the range of 30% to 95%.
【0007】[0007]
【作 用】上記のように構成されたサンプル容器によれ
ばサンプルは、樹脂と熱伝導の良好な無機充填材から成
る複合体部分の設置により、外部からの加熱、冷却を行
う温度プロセスを効率よくサンプルに伝える事を可能と
する。サンプルに対しても無機充填材が直接接触するこ
となくサンプルにダメージを与えることはない。またサ
ンプル容器の外部表面のサンプル容器保持体と接する部
分の構成成分樹脂がサンプル容器の主体成分樹脂より柔
軟な樹脂を使用することによりサンプル容器保持体とサ
ンプル容器の密着が可能となる。[Operation] According to the sample container configured as described above, the sample can be efficiently heated and cooled from the outside by installing a composite part made of resin and an inorganic filler with good thermal conductivity. It is possible to communicate well to the sample. The inorganic filler does not directly contact the sample and does not damage the sample. Further, by using a resin that is softer than the main component resin of the sample container as the constituent resin of the portion of the outer surface of the sample container that contacts the sample container holder, the sample container holder and the sample container can be brought into close contact with each other.
【0008】[0008]
【実施例1】図1は、本発明の実施例1の外観を示す。
図2は、図1のA−A断面である。実施例1のサンプル
容器は図2の断面構成に示すように、炭化ケイ素の粉体
から成る充填材とポリプロピレン樹脂から成る複合体高
熱伝導部1と、サンプルに充填材が直接に接触すること
のないようにポリプロピレン樹脂のみの2部から成って
いる。本サンプル容器の製法は、2多層ブロー成形とし
た。すなわち樹脂に体積配合比率をそれぞれ0、20、
30、50、70、80、90%の1μm〜20μmの
炭化ケイ素粉末を充填材として配合し複合体高熱伝導部
1とし、2の部分はポリプロピレン樹脂のみとし、厚さ
30μmとした。それぞれの容器の内部に熱電対を貼
り、それぞれの容器を80℃恒温水槽にセットし同条件
すなわち80℃の恒温水槽にサンプル容器を入れ、熱電
対の温度が常温から70℃になる時間を測定した。結果
は図3に示した。図からもわかるように本発明の範囲外
である充填材の体積配合比率30%未満では複合体高熱
伝導部1の熱伝導率が十分ではない。充填材の体積配合
比率が高ければ高いほど良好な結果であるが充填材の体
積配合比率が高いと強度劣化等の問題が起こる。よって
容器の強度及び容器の使用状態等を考慮して充填材の体
積配合比率を30%から95%の間で自由に選べばよ
い。ここでは無機充填材として炭化ケイ素の粒子を使用
しているがこれに限られるものではなく10W/(m
K)以上である無機充填材から形状も粒子及びウィスカ
ー及び繊維及び箔等から目的に合わせて自由に選べばよ
い。また本実施例では、2層のみであったが必要に応じ
て3層すなわち、1部と2部の層の間に緩和層を設けて
もよい。この層を設ける事により1層と2層の剪断応力
を緩和する事ができる。また内部のサンプルに接触する
部分2は本実施例では部分1と同様のポリプロピレンで
あるがこれに限られるものではなくサンプルおよび印加
する温度プロセスの目的、容器強度等に応じて部分1及
び部分2の樹脂材料を選ばよい。このサンプルに接触す
る部分2の製法も2色ブロー成型に限られるものでなく
複合体高熱伝導部のみの容器の成型を行ったのち内部の
サンプルに接触する部分2の樹脂のみの部分をコーティ
ングによって形成してもよい。Embodiment 1 FIG. 1 shows the appearance of Embodiment 1 of the present invention.
FIG. 2 is a cross section taken along the line AA of FIG. As shown in the cross-sectional structure of FIG. 2, the sample container of Example 1 has a composite high thermal conductive part 1 made of a filler of silicon carbide powder and a polypropylene resin, and the filler is in direct contact with the sample. Made of 2 parts of polypropylene resin only so that there is no. The manufacturing method of this sample container was two-layer blow molding. That is, the volume blending ratio of the resin is 0, 20, respectively.
30, 50, 70, 80, 90% of 1 μm to 20 μm of silicon carbide powder was blended as a filler to form the composite high thermal conductive portion 1, and the portion 2 was made of polypropylene resin only and had a thickness of 30 μm. Attach a thermocouple inside each container, set each container in a constant temperature water bath at 80 ° C, and put the sample container in the same temperature water bath at 80 ° C, and measure the time when the temperature of the thermocouple changes from room temperature to 70 ° C. did. The results are shown in Fig. 3. As can be seen from the figure, the thermal conductivity of the composite high thermal conductivity part 1 is not sufficient when the volume ratio of the filler is less than 30%, which is outside the scope of the present invention. The higher the volume blending ratio of the filler, the better the result. However, the higher volume blending ratio of the filler causes problems such as strength deterioration. Therefore, the volume mixture ratio of the filler may be freely selected from 30% to 95% in consideration of the strength of the container, the usage state of the container, and the like. Here, particles of silicon carbide are used as the inorganic filler, but the present invention is not limited to this, and 10 W / (m
The shape may be freely selected from particles and whiskers, fibers, foils and the like from the above-mentioned inorganic fillers according to the purpose. Further, in this embodiment, only two layers are provided, but if necessary, three layers, that is, a relaxation layer may be provided between the one part and the two parts. By providing this layer, the shear stress of the first and second layers can be relaxed. In the present embodiment, the portion 2 that contacts the sample is the same polypropylene as the portion 1, but the present invention is not limited to this, and the portion 1 and the portion 2 may be selected depending on the purpose of the sample and the temperature process to be applied, the container strength, and the like. Any resin material may be selected. The manufacturing method of the part 2 contacting with the sample is not limited to the two-color blow molding, but after molding the container having only the high thermal conductivity part of the composite, the part 2 contacting with the sample inside is coated with the resin only. You may form.
【0009】[0009]
【実施例2】実施例1で作成した容器の外側表面のサン
プル容器保持体と接する部分に図4に示すようにゲル化
処理を行うと弾力性をもつ銅粉を分散させたゲル状シリ
コン樹脂層を形成した。ここで図4の3の部分が弾力性
をもつ銅粉を分散させたゲル状シリコン樹脂層で出あ
る。図5は図4のA−A断面である。この部分の形成方
法は、実施例1で作成した炭化ケイ素充填材の体積配合
比率70%の容器に、ゲル化前のシリコーン樹脂に無機
充填材としての銅粉を加え一様に分布させるために界面
活性剤、分散剤等を加え撹拌市、溶剤を用い粘度を調整
したものを塗布する。そしてこの部分に対してゲル化処
理を行う。本実施例では、熱によるゲル化処理を行っ
た。次にこの容器の性能をテストするために図5に示す
ようにドライ恒温槽のアルミブロック4に柔軟部分を設
置した容器と設置していない容器を挿入し比較試験を行
った。アルミブロックを80℃に設定しておきそれぞれ
の容器を容器保持部分に挿入し容器と容器保持部の密着
性を高めるためにサンプル容器上部に重りを置いた。そ
して実施例1と同様に70℃までの到達時間を測定し
た。結果は柔軟部分を設置した容器のほうが柔軟部分を
設置していない容器に比較して80%到達時間が短縮で
きた。本実施例では柔軟部分の設置を塗布によって行っ
たがこれに限られるものではない。例えば容器の成型の
時同時に行ってもよい。すなわちインジェクションなど
の方法で3色成型を行ってもよい。もちろん柔軟部分は
本発明の範囲の材料を選べばよい。すなわちサンプル容
器の外部表面のサンプル容器保持体と接する部分の構成
成分樹脂の引っ張り強度が32MPa以下あるいは縦弾
性率が1.4GPa以下あるいは、軟化温度が100℃
以下の樹脂から目的に応じた樹脂を選んでもよい。また
1部の複合体高熱伝導部と3部の柔軟部分の間に緩和層
を設けてもよい。この層を設ける事により2層と3層の
剪断応力を緩和する事ができる。この柔軟部分3に分散
されている無機充填材は銅粉に限られるものではない。
10W/(mK)以上である無機充填材から形状も粒子
及びウィスカー及び繊維及び箔等から目的に合わせて自
由に選べばよい。[Example 2] A gel-like silicone resin in which copper powder having elasticity is dispersed when a gelation treatment is performed on a portion of the outer surface of the container prepared in Example 1 in contact with the sample container holder as shown in FIG. Layers were formed. Here, the portion 3 in FIG. 4 is a gel silicon resin layer in which copper powder having elasticity is dispersed. FIG. 5 is a cross section taken along line AA of FIG. This part is formed by adding copper powder as an inorganic filler to the silicone resin before gelation in a container having a volume ratio of 70% of the silicon carbide filler prepared in Example 1 so as to be uniformly distributed. Add a surfactant, dispersant, etc. and stir it, and apply a solution whose viscosity has been adjusted using a solvent. Then, gelation treatment is performed on this portion. In this example, gelation treatment by heat was performed. Next, in order to test the performance of this container, as shown in FIG. 5, a container in which a flexible portion was installed and a container in which it was not installed were inserted into an aluminum block 4 of a dry thermostat and a comparative test was performed. The aluminum block was set to 80 ° C., each container was inserted into the container holding portion, and a weight was placed on the upper part of the sample container in order to enhance the adhesion between the container and the container holding portion. Then, as in Example 1, the time required to reach 70 ° C. was measured. As a result, the arrival time of the container having the flexible portion was shortened by 80% as compared with the container having no flexible portion. In this embodiment, the flexible portion is installed by coating, but the invention is not limited to this. For example, it may be performed at the same time when the container is molded. That is, three-color molding may be performed by a method such as injection. Of course, for the flexible portion, a material within the scope of the present invention may be selected. That is, the tensile strength of the component resin on the outer surface of the sample container in contact with the sample container holder is 32 MPa or less, the longitudinal elastic modulus is 1.4 GPa or less, or the softening temperature is 100 ° C.
You may select the resin according to the purpose from the following resins. A relaxation layer may be provided between one part of the high thermal conductivity composite part and three parts of the flexible part. By providing this layer, the shear stress of the second and third layers can be relaxed. The inorganic filler dispersed in the flexible portion 3 is not limited to copper powder.
The shape can be freely selected from particles and whiskers, fibers, foils and the like from the inorganic filler having a power of 10 W / (mK) or more.
【0010】[0010]
【実施例3】図7に実施例3のサンプル容器の外観を示
す。図8は図7のA−A断面出ある。ここで7部は無機
充填材として窒化ホウ素粒子を体積配合比率60%と
し、樹脂はエポキシを使用した8部はポリプロピレン、
9部は窒化ホウ素粒子を分散させた軟質PVCを使用し
た。実施例2と同様のテストを行った。すなわち比較の
ため図9に示すように、無機充填材の配合がないエポキ
シ樹脂のみの部分10とポリプロピレン部分11とから
なるサンプル容器を用意する。図10に示すようにアル
ミブロック12にサンプル容器13をセットしそれぞれ
のサンプル容器13はロッド14で上方より押し付け
た。サンプル容器のサンプル保持部分の底面15部に熱
電対を貼りテストを行った。結果は70℃到達温度は本
実施例のほうが比較例に対して1/7の時間となり良好
な結果を示した。以上本発明を実施例に基き具体的に説
明したが、本発明は、前記実施例に限定されるものでは
なく、その要旨を逸脱しない範囲で種々の変更可能であ
ることはいうまでもない。Third Embodiment FIG. 7 shows the appearance of the sample container of the third embodiment. FIG. 8 shows an AA cross section of FIG. 7. Here, 7 parts are boron nitride particles as an inorganic filler in a volume mixture ratio of 60%, 8 parts using epoxy as a resin are polypropylene,
Nine parts used soft PVC in which boron nitride particles were dispersed. The same test as in Example 2 was performed. That is, for comparison, as shown in FIG. 9, a sample container including a portion 10 containing only an epoxy resin containing no inorganic filler and a polypropylene portion 11 is prepared. As shown in FIG. 10, the sample containers 13 were set on the aluminum block 12, and each sample container 13 was pressed by the rod 14 from above. A test was conducted by attaching a thermocouple to the bottom part 15 of the sample holding part of the sample container. As a result, the temperature reached to 70 ° C. was 1/7 of that of the comparative example, which was a good result. Although the present invention has been specifically described based on the embodiments, the present invention is not limited to the above embodiments, and it goes without saying that various modifications can be made without departing from the scope of the invention.
【0011】[0011]
【発明の効果】以上のように、本発明は、外部からの加
熱、冷却を行う温度プロセスを迅速に効率よくサンプル
に伝える事を可能にした高熱伝導高熱伝達なサンプル容
器である。バイオテクノロジー分野及び化学及び医学、
工学に関係する分野において、新しい用途と応用の道を
開いて行くための発明である。INDUSTRIAL APPLICABILITY As described above, the present invention is a sample container having high heat conduction and high heat transfer capable of rapidly and efficiently transmitting the temperature process of heating and cooling from the outside to the sample. Biotechnology and chemistry and medicine,
It is an invention for paving the way for new applications and applications in fields related to engineering.
【図1】実施例1の外観FIG. 1 Appearance of Example 1
【図2】図1のA−A断面FIG. 2 is a sectional view taken along line AA of FIG.
【図3】実施例1の実験結果FIG. 3 is an experimental result of Example 1.
【図4】実施例2の外観FIG. 4 Appearance of Example 2
【図5】図4のA−A断面5 is a cross section taken along line AA of FIG.
【図6】実施例2のテスト状態6 is a test state of Example 2. FIG.
【図7】実施例3の外観FIG. 7 Appearance of Example 3
【図8】図7のA−A断面8 is a cross section taken along line AA of FIG.
【図9】比較例の断面FIG. 9 is a cross section of a comparative example.
【図10】実施例3のテスト状態FIG. 10: Test state of Example 3
1 高熱伝導部分 2 サンプル接触部分 3 柔軟層 4 アルミニウムブロック 5 サンプル容器 6 重り 7 高熱伝導部分 8,11 サンプル接触部分 9 柔軟層 12 アルミニウムブロック 13 サンプル容器 14 ロッド 1 High Thermal Conduction Part 2 Sample Contact Part 3 Flexible Layer 4 Aluminum Block 5 Sample Container 6 Weight 7 High Thermal Conductivity Part 8, 11 Sample Contact Part 9 Flexible Layer 12 Aluminum Block 13 Sample Container 14 Rod
Claims (14)
ル容器で、その構成材の成分が樹脂と無機充填材から成
る事を特徴とするサンプル容器。1. A sample container having one or more sample holding parts, wherein the components of the sample container are composed of a resin and an inorganic filler.
成され、残部は樹脂と無機充填材の複合体から構成され
た少なくとも2つの部分からなる構造を特徴とする特許
請求範囲第1項記載のサンプル容器。2. The structure according to claim 1, wherein the portion in contact with the sample is composed only of resin, and the remaining portion is composed of at least two portions composed of a composite of resin and inorganic filler. Sample container.
保持体と接する部分の構成成分樹脂がサンプル容器の主
体成分樹脂より柔軟な樹脂である事を特徴とする特許請
求範囲第1項記載のサンプル容器。3. The sample container according to claim 1, wherein the constituent resin of the portion of the outer surface of the sample container which is in contact with the sample container holder is softer than the main component resin of the sample container. .
された部分と、樹脂と無機充填材の複合体部分及びサン
プル容器の外部表面のサンプル容器保持体と接する部分
の構成成分樹脂がサンプル容器の主体成分より変形容易
な樹脂であるそれぞれ部分の境界層の少なくとも1層部
分に膨張係数の違いによる破壊防止を目的とするポリマ
ー接着の方法で応力緩和層を設けた構造を特徴とする特
許請求範囲第2項及び第3項記載のサンプル容器。4. The component resin of the portion of the sample container which is in contact with the sample and is composed only of the resin, the composite portion of the resin and the inorganic filler and the portion of the outer surface of the sample container which is in contact with the sample container holder are A structure in which a stress relaxation layer is provided by a method of polymer adhesion for the purpose of preventing breakage due to a difference in expansion coefficient in at least one layer part of the boundary layer of each part that is a resin that is more easily deformable than the main component. The sample container according to the second and third aspects.
5%である事を特徴とする特許請求範囲第1項記載のサ
ンプル容器。5. The volume content of the inorganic filler is 30% to 9%.
It is 5%, The sample container of Claim 1 characterized by the above-mentioned.
K)以上であるセラミックス、金属、カーボンから選ば
れる少なくとも1つの材質である事を特徴とする特許請
求範囲第1項記載のサンプル容器。6. The inorganic filler has a thermal conductivity of 10 W / (m
The sample container according to claim 1, wherein the sample container is made of at least one material selected from the group consisting of ceramics, metals, and carbon which is K) or more.
維及び箔から選ばれた少なくとも一種の形状である事を
特徴とする特許請求範囲第1項記載のサンプル容器。7. The sample container according to claim 1, wherein the inorganic filler has at least one shape selected from particles and whiskers, fibers and foils.
ウム、炭化ケイ素、窒化ケイ素、炭酸カルシウム、酸化
マグネシウム、酸化ケイ素、石英ガラス、酸化ジルコニ
ウム、窒化チタン、酸化ベリリウム、カーボン、ダイヤ
モンド、金、銀、銅、アルミニウム、タングステン、モ
リブデンから選ばれた少なくとも1つの材料を主成分と
する事を特徴とする特許請求範囲第1項記載のサンプル
容器。8. The inorganic filler is boron nitride, aluminum oxide, silicon carbide, silicon nitride, calcium carbonate, magnesium oxide, silicon oxide, quartz glass, zirconium oxide, titanium nitride, beryllium oxide, carbon, diamond, gold, silver, The sample container according to claim 1, characterized in that at least one material selected from copper, aluminum, tungsten, and molybdenum is a main component.
部分の厚さが5μm〜200μmである事を特徴とする
特許請求範囲第2項記載のサンプル容器。9. The sample container according to claim 2, wherein the thickness of the portion which is in contact with the sample and is composed only of the resin is 5 μm to 200 μm.
器保持体と接する部分の構成成分樹脂がサンプル容器の
主体成分樹脂より柔軟な樹脂である部分の厚さが5μm
〜300μmである事を特徴とする特許請求範囲第3項
記載のサンプル容器。10. The thickness of the portion of the outer surface of the sample container, which is softer than the main component resin of the sample container, of the component resin of the part in contact with the sample container holder has a thickness of 5 μm.
The sample container according to claim 3, wherein the sample container has a thickness of 300 μm.
器保持体と接する部分の構成成分樹脂の引っ張り強度が
32MPa以下である事を特徴とする特許請求範囲第3
項記載のサンプル容器。11. The tensile strength of the constituent resin at the portion of the outer surface of the sample container which is in contact with the sample container holder is 32 MPa or less.
Item sample container.
器保持体と接する部分の構成成分樹脂の縦弾性率が1.
4GPa以下である事を特徴とする特許請求範囲第3項
記載のサンプル容器。12. The longitudinal elastic modulus of the constituent resin of the portion of the outer surface of the sample container which is in contact with the sample container holder is 1.
It is 4 GPa or less, The sample container of Claim 3 characterized by the above-mentioned.
器保持体と接する部分の構成成分樹脂がゲル状であるあ
る事を特徴とする特許請求範囲第3項記載のサンプル容
器。13. The sample container according to claim 3, wherein the component resin of the portion of the outer surface of the sample container which is in contact with the sample container holder is gel.
器保持体と接する部分の構成成分樹脂の軟化温度が10
0℃以下である事を特徴とする特許請求範囲第3項記載
のサンプル容器。14. The softening temperature of the constituent resin of the portion of the outer surface of the sample container which is in contact with the sample container holder is 10.
The sample container according to claim 3, wherein the sample container has a temperature of 0 ° C or lower.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24348594A JPH07125739A (en) | 1993-09-03 | 1994-09-01 | Sample container |
| PCT/JP1995/000273 WO1996026008A1 (en) | 1994-09-01 | 1995-02-24 | Sample container |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25354693 | 1993-09-03 | ||
| JP5-253546 | 1993-09-03 | ||
| JP24348594A JPH07125739A (en) | 1993-09-03 | 1994-09-01 | Sample container |
| PCT/JP1995/000273 WO1996026008A1 (en) | 1994-09-01 | 1995-02-24 | Sample container |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07125739A true JPH07125739A (en) | 1995-05-16 |
Family
ID=26536278
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24348594A Pending JPH07125739A (en) | 1993-09-03 | 1994-09-01 | Sample container |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07125739A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001094018A1 (en) * | 2000-06-07 | 2001-12-13 | Evotec Oai Ag | Micro-titre plate or chip with an embedded support core |
| WO2022230660A1 (en) * | 2021-04-26 | 2022-11-03 | パナソニックIpマネジメント株式会社 | Heat insulating container |
-
1994
- 1994-09-01 JP JP24348594A patent/JPH07125739A/en active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001094018A1 (en) * | 2000-06-07 | 2001-12-13 | Evotec Oai Ag | Micro-titre plate or chip with an embedded support core |
| JP2003535350A (en) * | 2000-06-07 | 2003-11-25 | エボテック・オーアーイー・アーゲー | Sample holder |
| US7455815B2 (en) | 2000-06-07 | 2008-11-25 | Evotec Ag | Micro-titre plate or chip with an embedded support core |
| WO2022230660A1 (en) * | 2021-04-26 | 2022-11-03 | パナソニックIpマネジメント株式会社 | Heat insulating container |
| CN116601085A (en) * | 2021-04-26 | 2023-08-15 | 松下知识产权经营株式会社 | Thermal insulation container |
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