JPH01211A - Method for producing gold particles - Google Patents
Method for producing gold particlesInfo
- Publication number
- JPH01211A JPH01211A JP62-154777A JP15477787A JPH01211A JP H01211 A JPH01211 A JP H01211A JP 15477787 A JP15477787 A JP 15477787A JP H01211 A JPH01211 A JP H01211A
- Authority
- JP
- Japan
- Prior art keywords
- gold particles
- iodide
- particle size
- fine gold
- particles
- 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
- 239000002245 particle Substances 0.000 title claims description 32
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 title claims description 22
- 239000010931 gold Substances 0.000 title claims description 21
- 229910052737 gold Inorganic materials 0.000 title claims description 20
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 8
- 239000000243 solution Substances 0.000 claims description 8
- 150000002500 ions Chemical class 0.000 claims description 6
- 239000003945 anionic surfactant Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- GCZKMPJFYKFENV-UHFFFAOYSA-K triiodogold Chemical compound I[Au](I)I GCZKMPJFYKFENV-UHFFFAOYSA-K 0.000 claims description 5
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims description 2
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical class [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
- 229910001516 alkali metal iodide Inorganic materials 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 235000009518 sodium iodide Nutrition 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 229940107816 ammonium iodide Drugs 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000011575 calcium Chemical class 0.000 description 1
- 229910001640 calcium iodide Inorganic materials 0.000 description 1
- 229940046413 calcium iodide Drugs 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- -1 iodine ions Chemical class 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 239000011777 magnesium Chemical class 0.000 description 1
- BLQJIBCZHWBKSL-UHFFFAOYSA-L magnesium iodide Chemical compound [Mg+2].[I-].[I-] BLQJIBCZHWBKSL-UHFFFAOYSA-L 0.000 description 1
- 229910001641 magnesium iodide Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- JLKDVMWYMMLWTI-UHFFFAOYSA-M potassium iodate Chemical compound [K+].[O-]I(=O)=O JLKDVMWYMMLWTI-UHFFFAOYSA-M 0.000 description 1
- 239000001230 potassium iodate Substances 0.000 description 1
- 235000006666 potassium iodate Nutrition 0.000 description 1
- 229940093930 potassium iodate Drugs 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
（産業上の利用分野）
本発明は微細な金微粒子の製造方決に関するものである
。DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a method for producing fine gold particles.
（従来技術とその問題点）
従来金微粒子の製造方法としては、塩化金酸溶液などに
ヒドラジン等の還元酸剤を用いて還元する方法が用いら
れてきた。(Prior art and its problems) As a conventional method for producing fine gold particles, a method has been used in which a chloroauric acid solution or the like is reduced using a reducing acid such as hydrazine.
ところが、この方法では、還元された粒子同士が引き寄
せ合うために、凝集してしまい粒度分布の幅の広い金微
粒子しか得られないという欠点を有していた。However, this method has the disadvantage that the reduced particles are attracted to each other and aggregate, resulting in only fine gold particles with a wide particle size distribution being obtained.
（発明の目的）
発明者は、ヨウ化金を溶かしたヨウ化カリウム溶液〔（
１）、（２）式〕に、水酸化カリウム溶液を加えると、
金微粒子が得られる事〔（３）式〕に着目したが、こ方
法により得られる粒子は、数μから数十μの粒径のもで
あり、数μ以下の金微粒子を得ることは難しかった。(Object of the invention) The inventor has developed a potassium iodide solution [(
When potassium hydroxide solution is added to equations 1) and (2),
We focused on the fact that fine gold particles can be obtained [Equation (3)], but the particles obtained by this method have a particle size of several microns to several tens of microns, and it is difficult to obtain fine gold particles with a size of several microns or less. Ta.
Ｋ Ｉ ＋ Ａ ｕ Ｅ ｘ Ｋ Ａ ｕ ｌ
ａ −−−−−−−−−−（１）ＫＡｕ １４
Ｋ”＋ （Ａｕ １４） −−−−−−ｆ
２１２ （ＡｕＩ＊） −＋６ＫＯＨ→２Ａｕ↓＋５Ｋ
Ｉ＋に１０ｚ＋３８ｔＯ＋２ｌ−−−（３１本発明は上
記の欠点を解消せんがためになされたものであり、分散
した、粒度分布の幅の狭い粒径コントロール可能な微細
な金微粒子の製造方法を提供せんとするものである。K I + A u Ex x K A u l
a ----------(1) KAu 14
K”+ (Au 14) −−−−−−f
212 (AuI*) -+6KOH→2Au↓+5K
I + 10z + 38tO + 2l --- (31 The present invention has been made to solve the above-mentioned drawbacks, and provides a method for producing fine gold particles that are dispersed and have a narrow particle size distribution and whose particle size can be controlled. That is.
（問題点を解決するための手段）
微細な金微粒子を得る為に、ヨウ化金酸イオンを含む水
溶液に水酸化アルカリ金属溶液を加え、金を析出させる
方法において、あらかじめ反応溶液中にアニオン系界面
活性剤を添加しておくことを特徴とするものである。(Means for solving the problem) In order to obtain fine gold particles, an alkali metal hydroxide solution is added to an aqueous solution containing iodoaurate ions to precipitate gold. It is characterized by the addition of a surfactant.
この方法により得られる金微粒子は、数ミクロン以下の
粒度分の幅の狭いものである。The fine gold particles obtained by this method have a narrow particle size of several microns or less.
ヨウ化金酸イオンを含む水溶液のｐｉ（は１３以下が良
く、ｐＨ１３を超えると（３）式の反応がおこてしまう
ため、目的とする金微粒子が得られなくなる。The pH of the aqueous solution containing iodoauric acid ions is preferably 13 or less; if the pH exceeds 13, the reaction of formula (3) will occur, making it impossible to obtain the desired gold particles.
またこの水溶液のｐＨは、アルカリを加える都合上８〜
１３位が良い。In addition, the pH of this aqueous solution is 8 to 8 to account for the addition of alkali.
13th place is good.
ヨウ化金をヨウ化アルカリ金属塩にとかした場合ｐＨは
、中性から弱酸性（ｐＨ３〜８位）を示す。−ｐＨを調
整する為には、酸としては硫酸、塩。When gold iodide is dissolved in an alkali metal iodide salt, the pH ranges from neutral to weakly acidic (pH 3 to 8). - To adjust the pH, use sulfuric acid or salt as the acid.
酸、硝酸、ヨウ化水素酸、リン酸、酢酸等が上げられる
。アルカリとしては、水酸化ナトリウム、水酸化カリウ
ム、アンモニア水等があげられる。Examples include acids, nitric acid, hydroiodic acid, phosphoric acid, and acetic acid. Examples of the alkali include sodium hydroxide, potassium hydroxide, and aqueous ammonia.
また反応前の掻端なｐＨの変動をを抑えるためにｐ）（
の緩衝作用を有する塩や、酸、アルカリとの組合わせ例
えば、リン酸水素２ナトリウム−リン酸２水素ナトリウ
ム、炭酸水素ナトリウム−炭酸ナトリウム、炭酸ナトリ
ウム−水酸化ナトリウム、酢酸−酢酸ナトリウム等によ
りｐＨ調整しても良い。In addition, in order to suppress drastic pH fluctuations before the reaction, p)(
Combinations with salts, acids, and alkalis that have the buffering effect of You can adjust it.
ヨウ化金酸イオンを含む水溶液を得るためのヨウ化金塩
としてはヨウ化合カリウム、ヨウ化合ナトリウムの他に
、Ｍｇ塩、Ｃａ塩、ＮＨ４塩等があげられる。またヨウ
化金をヨウ化塩（Ｋｌ、Ｎａｌ、Ｍｇ１など）にとかし
ても良い。Examples of gold iodide salts for obtaining an aqueous solution containing iodoauric acid ions include potassium iodide, sodium iodide, Mg salt, Ca salt, NH4 salt, and the like. Alternatively, gold iodide may be dissolved in iodide salt (Kl, Nal, Mg1, etc.).
ヨウ化金をヨウ化アルカリ金属塩に溶かしたヨウ化金酸
イオンを含む水溶液でヨウ化アルカリ金属塩濃度は０．
５〜５Ｍ／１位が良い。An aqueous solution containing iodoaurate ions in which gold iodide is dissolved in an alkali metal iodide salt, and the alkali metal iodide concentration is 0.
5-5M/1st place is good.
高濃度では、ヨウ化アルカリ金属の飽和濃度に近く結晶
が出やすいこと、反応が終わって、ヨウ素イオンが過剰
になり、塩析効果により、金粉の析出に伴い生成するヨ
ウ素酸カリウムが金粉とともに析出してしまうなどがあ
げられる。At high concentrations, crystals tend to form as it approaches the saturation concentration of alkali metal iodide, and after the reaction ends, iodine ions become excessive, and due to the salting-out effect, potassium iodate, which is generated as gold powder is precipitated, precipitates together with the gold powder. Examples include:
反応温度は粒子の粒径を揃える為に、好ましくは２０〜
７０℃の間で一定に保つほうが良く、温度条件を変える
ことにより粒径のコントロールができる。The reaction temperature is preferably 20~20 to make the particle size uniform.
It is better to keep the temperature constant at 70°C, and the particle size can be controlled by changing the temperature conditions.
水酸化アルカリ濃度は、０．１〜６Ｎ位が良い。The alkali hydroxide concentration is preferably about 0.1 to 6N.
０、ＩＮ未満では反応に大量の水酸化アルカリ溶液を必
要とし、６Ｎを超えると、金微粒子が凝集し易くなるか
らである。This is because if it is less than 0.0N, a large amount of alkaline hydroxide solution is required for the reaction, and if it exceeds 6N, the gold fine particles tend to aggregate.
反応の終点のｐＨは、２０℃では１２６５以上、８０℃
では、１２．０以上であれば良いが終点のｐＨが低いと
歩留りが悪くなるので好ましくはｐＨ１３以上である。The pH at the end of the reaction is 1265 or higher at 20°C and 80°C.
In this case, it is sufficient if the pH is 12.0 or higher, but if the pH at the end point is low, the yield will be poor, so the pH is preferably 13 or higher.
実施例においてはアルカリ金属としてヨウ化カリウムを
用いたがその他にヨウ化ナトリウム、ヨウ化カルシウム
やヨウ化マグネシウム、ヨウ化アンモニウム等でも良い
。In the examples, potassium iodide was used as the alkali metal, but sodium iodide, calcium iodide, magnesium iodide, ammonium iodide, etc. may also be used.
以上の作用のもとに本発明において反応溶液中にはアニ
オン系界面活性剤を添加する理由は、水溶液中に析出し
た金微粒子が凝集しないで単分散状態を保たせる為と、
−旦析出した金微粒子を核に結晶成長することを防止す
る為である。Based on the above effects, the reason why an anionic surfactant is added to the reaction solution in the present invention is to keep the gold fine particles precipitated in the aqueous solution from agglomerating and to maintain a monodisperse state.
- This is to prevent crystal growth using the fine gold particles that have already precipitated as nuclei.
本発明において反応溶液中に添加するアニオン系界面活
性剤としてはサーフロン５ｉｌｌ、同１１２、同１１３
等がある。In the present invention, the anionic surfactants added to the reaction solution include Surflon 5ill, Surflon 112, and Surflon 113.
etc.
（実施例１）
３、ＯＮの水酸化カリウム溶液２００ ｄに７ニオン系
界面活性剤サーフロンＳ−１１１を（５ｇ／Ｊ）５０−
を加えあらかじめ、３０℃に加温しておく。(Example 1) 3. 7-ionic surfactant Surflon S-111 was added to 200 d of ON potassium hydroxide solution (5 g/J) 50-
Add and warm to 30℃ in advance.
１ｉビーカーにＩＩｌ当りヨウ化カリウム１．０Ｍヨウ
化合金０．１を含みｐＨ１１，０に調整したヨウ化金酸
イオンを含む水溶液５００−をとり、３０℃迄加温して
おき、これに先の水酸化カリウム＋界面活性側溶液中に
添加すると、暗黄色の沈殿物が得られる。In a 1i beaker, take 500ml of an aqueous solution containing 1.0M potassium iodide and iodide alloy 0.1 per IIl and containing iodoauric acid ions adjusted to pH 11.0, warm it to 30°C, and pre-heat it to 30°C. When added to the potassium hydroxide + surfactant side solution, a dark yellow precipitate is obtained.
これをデカンチーシランにて洗浄し、粒度分布測定及び
電子顕微鏡観察を行ったところ、図及び表に示す結果を
得た。This was washed with decanty silane and subjected to particle size distribution measurement and electron microscope observation, and the results shown in the figure and table were obtained.
（実施例２）
実施例１において反応温度を５０℃としたものについて
行ったところ、図及び表に示す結果を得た。(Example 2) When the reaction temperature was set to 50° C. in Example 1, the results shown in the figure and table were obtained.
（実施例３）
実施例１においてアニオン系界面活性剤の濃度を２０ｇ
／ｌとしたものについて行ったところ、図及び表に示す
結果を得た。(Example 3) In Example 1, the concentration of anionic surfactant was 20g.
/l, the results shown in the figure and table were obtained.
（比較例）
実施例・１においてアニオン系界面活性剤を加えない条
件で行ったところ図及び表に示す結果を得た。(Comparative Example) When Example 1 was carried out without adding an anionic surfactant, the results shown in the figure and table were obtained.
（発明の効果）
以上の説明かられかるように本発明による金微粒子の製
造方法は、従来法では得られなかった粒度分布の幅の狭
い、微細な金微粒子を、粒径及び形状をコントロールし
て製造できるので、従来の製造方法に比べ画期的なもの
といえる。(Effects of the Invention) As can be seen from the above explanation, the method for producing fine gold particles according to the present invention can control the particle size and shape of fine gold particles with a narrow particle size distribution that could not be obtained by conventional methods. Since it can be manufactured using multiple steps, it can be said to be revolutionary compared to conventional manufacturing methods.
図は光透過式粒度分布測定装置を用いて各金微粒子の粒
度分布を測定した結果を横軸に粒径、縦軸に累積パーセ
ントを取って示したものである。
出願人 田中貴金属工業株式会社
−顕零°く−ν入−The figure shows the results of measuring the particle size distribution of each fine gold particle using a light transmission type particle size distribution measuring device, with the horizontal axis representing the particle diameter and the vertical axis representing the cumulative percentage. Applicant: Tanaka Kikinzoku Kogyo Co., Ltd.
Claims (1)
、ヨウ化金を分解し、金微粒子を製造する方法において
、反応溶液中にアニオン系界面活性剤を添加することに
より単分散した金微粒子を得ることを特徴とする金微粒
子の製造方法。In the method of producing fine gold particles by adding alkali hydroxide to an aqueous solution containing iodoaurate ions to decompose gold iodide, monodisperse fine gold particles can be produced by adding an anionic surfactant to the reaction solution. A method for producing fine gold particles, characterized in that:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15477787A JPS64211A (en) | 1987-06-22 | 1987-06-22 | Production of fine gold particles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15477787A JPS64211A (en) | 1987-06-22 | 1987-06-22 | Production of fine gold particles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01211A true JPH01211A (en) | 1989-01-05 |
| JPS64211A JPS64211A (en) | 1989-01-05 |
Family
ID=15591666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15477787A Pending JPS64211A (en) | 1987-06-22 | 1987-06-22 | Production of fine gold particles |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS64211A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004049902A (en) * | 1999-01-22 | 2004-02-19 | Adachi Kogyo:Kk | Slide-proof cut scissors |
-
1987
- 1987-06-22 JP JP15477787A patent/JPS64211A/en active Pending
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