JPS646159B2 - - Google Patents
Info
- Publication number
- JPS646159B2 JPS646159B2 JP58005431A JP543183A JPS646159B2 JP S646159 B2 JPS646159 B2 JP S646159B2 JP 58005431 A JP58005431 A JP 58005431A JP 543183 A JP543183 A JP 543183A JP S646159 B2 JPS646159 B2 JP S646159B2
- Authority
- JP
- Japan
- Prior art keywords
- solution
- crystals
- iron
- sio
- temperature
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B7/00—Single-crystal growth from solutions using solvents which are liquid at normal temperature, e.g. aqueous solutions
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/16—Oxides
- C30B29/18—Quartz
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Silicon Compounds (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Description
【発明の詳細な説明】
この発明は、耐火性酸化物である水晶を常温濃
縮現象を利用して製造する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing quartz, which is a refractory oxide, by utilizing a room temperature concentration phenomenon.
水晶は研磨材や時計の軸受、宝石、レコード針
等の広い用途をもつ。従来耐火性酸化物の単結晶
を得る方法としては、引上げ法、EFG法、
熱交換法、バクダザロフ法、ベルヌーイ
法、フラツクス法などが知られている。〜
はいずれも原材料をるつぼや容器に入れ、高温に
加熱して溶解し種子結晶下に成長させる方法であ
る。はるつぼや容器を使用しないが、原料を高
温で溶解する点で〜と同じである。は原材
料をフラツクス剤PbOや水晶石(Na3AlF6)を
用いてその融点より低い温度で溶解し、結晶を晶
出させる方法である。いずれの方法でも、少くと
も1000℃以上の高温にすることが必要となり、従
つてるつぼや溶器として白金、イリジユーム、モ
リブテン等の高融点金属材を用いなければならな
い。また高温溶解用炉や発熱体にも特殊な材料、
設備が要求される。 Quartz has a wide range of uses, including abrasive materials, watch bearings, jewelry, and record needles. Conventional methods for obtaining single crystals of refractory oxides include the pulling method, EFG method,
Known methods include the heat exchange method, Bakdazarov method, Bernoulli method, and flux method. ~
In both methods, raw materials are placed in a crucible or container, heated to high temperatures, melted, and grown under seed crystals. It is the same as ~ in that it does not use a crucible or container, but the raw materials are melted at high temperatures. This is a method in which raw materials are melted at a temperature lower than their melting point using a fluxing agent PbO or quartzite (Na 3 AlF 6 ) to crystallize crystals. In either method, it is necessary to raise the temperature to at least 1000°C or higher, and therefore a high melting point metal such as platinum, iridium, or molybdenum must be used as the crucible or melter. In addition, special materials are used for high-temperature melting furnaces and heating elements.
Equipment required.
この発明は、複雑かつ高価な設備を用いること
なく、常温濃縮現象を利用して簡便に水晶を製造
する方法を提供するものである。 The present invention provides a method for easily producing crystal using a room-temperature concentration phenomenon without using complicated and expensive equipment.
この発明の方法は、鉄(Fe)を含む溶液と二
酸化硅素(SiO2)を含む溶液を混合し、この混
合溶液に種子結晶を入れて放置することにより、
常温濃縮現象で水晶を成長させることを特徴とし
ている。 The method of this invention involves mixing a solution containing iron (Fe) and a solution containing silicon dioxide (SiO 2 ), and adding seed crystals to this mixed solution and leaving it to stand.
It is characterized by growing crystals through a room-temperature concentration phenomenon.
例えば、Feを4〜12規程の硝酸に溶解した溶
解液と、硅酸塩またはシリカゲルの水溶液を混合
して放置すると、溶液中に生じたSiO2を含むゲ
ル状物質中に水晶が晶出する。この結晶成長に
は、溶液中のFe(OH)3またはSiO2ゲルが触媒と
して作用しているもの考えられる。 For example, when a solution prepared by dissolving Fe in 4-12 nitric acid and an aqueous solution of silicate or silica gel are mixed and left to stand, crystals will crystallize in the gel-like substance containing SiO 2 produced in the solution. . It is thought that Fe(OH) 3 or SiO 2 gel in the solution acts as a catalyst for this crystal growth.
この発明の方法は、従来法のような高温を要せ
ず、常温付近で簡単に実施できることが基本的に
優れている点である。得られる水晶の大きさや成
長速度は、溶液のPH濃度、温度、過飽和度等の制
御により、また種子結晶を入れることにより、制
御される。 The basic advantage of the method of this invention is that it does not require high temperatures unlike conventional methods and can be easily carried out at around room temperature. The size and growth rate of the crystals obtained are controlled by controlling the pH concentration, temperature, degree of supersaturation, etc. of the solution, and by adding seed crystals.
以下この発明の実施例を説明する。100c.c.のビ
ーカーを2個用意し、一方のビーカーに8規程の
硝酸を約50c.c.計入れ、これに三価のFeを含む鉄
の棒(2mmφ×30mm)を入れた。更にPH濃度調整
のためNaOHを約5c.c.入れた。他方のビーカー
には水50c.c.を入れこれにシリカゲルを溶かして
SiO2濃度50ppmのシリカ溶液を作つた。これら
の溶液を交互に少しずつ混合して最終的に一方の
ビーカーに全部を入れ、これに水晶の種子結晶を
入れて5日間放置した。これにより、種子結晶上
に水晶結晶が生成された。更に上記実施例では
Feを溶解するのに硝酸を用いたが、硝酸と他の
酸の混液等を用いてもよい。更にまた、SiO2を
含む溶液についても、Na2SiO3やK2SiO3等、Fe
を含む溶液と混合したときにSiO2ゲルを生ずる
ような硅酸塩を溶かした水溶液を用いることがで
きる。 Examples of the present invention will be described below. Two 100 c.c. beakers were prepared, approximately 50 c.c. of 8N nitric acid was placed in one beaker, and an iron rod (2 mmφ x 30 mm) containing trivalent Fe was placed in the beaker. Furthermore, approximately 5 c.c. of NaOH was added to adjust the pH concentration. Pour 50 c.c. of water into the other beaker and dissolve the silica gel in it.
A silica solution with a SiO 2 concentration of 50 ppm was prepared. These solutions were mixed little by little alternately and finally all were put into one beaker, quartz seed crystals were added thereto, and the mixture was left for 5 days. As a result, quartz crystals were generated on the seed crystals. Furthermore, in the above example
Although nitric acid was used to dissolve Fe, a mixture of nitric acid and other acids may also be used. Furthermore, regarding solutions containing SiO 2 , Na 2 SiO 3 , K 2 SiO 3 , Fe
An aqueous solution of silicate can be used that produces a SiO 2 gel when mixed with a solution containing silicates.
この発明の効果を列記すれば次のとおりであ
る。(1)従来、少くとも1000℃以上の高温でなけれ
ば結晶成長ができなかつた水晶を常温付近できわ
めて簡便に作ることができる。(2)耐熱容器、高温
溶解設備など、複雑かつ高価な装置や設備を要せ
ず、従つて安価な水晶を提供できる。(3)結晶成長
は種子結晶上に行うことができ、溶液のPH濃度の
制御等により、水晶のエピタキシヤル成長も可能
である。 The effects of this invention are listed below. (1) Quartz crystals, which conventionally could only be grown at high temperatures of at least 1000°C, can be produced extremely easily at room temperature. (2) Complex and expensive devices and equipment such as heat-resistant containers and high-temperature melting equipment are not required, and therefore inexpensive crystal can be provided. (3) Crystal growth can be performed on seed crystals, and epitaxial growth of crystals is also possible by controlling the pH concentration of the solution.
Claims (1)
し、この混合溶液に種子結晶を入れて、常温に放
置して水晶を析出させることを特徴とする水晶の
製造方法。 2 鉄を含む溶液は鉄を4〜12規程の硝酸に溶解
した溶液であり、二酸化硅素を含む溶液は硝酸塩
またはシリカゲルを水に溶解した溶液である特許
請求の範囲第1項記載の水晶の製造方法。[Scope of Claims] 1. A method for producing crystals, which comprises mixing a solution containing iron and a solution containing silicon dioxide, adding seed crystals to the mixed solution, and leaving the mixture at room temperature to precipitate crystals. 2. Production of crystal according to claim 1, wherein the iron-containing solution is a solution in which iron is dissolved in 4-12 standard nitric acid, and the silicon dioxide-containing solution is a solution in which nitrate or silica gel is dissolved in water. Method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58005431A JPS58190900A (en) | 1983-01-17 | 1983-01-17 | Production of quartz crystal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58005431A JPS58190900A (en) | 1983-01-17 | 1983-01-17 | Production of quartz crystal |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11875880A Division JPS5854119B2 (en) | 1980-08-28 | 1980-08-28 | Production method of α-alumina single crystal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58190900A JPS58190900A (en) | 1983-11-07 |
| JPS646159B2 true JPS646159B2 (en) | 1989-02-02 |
Family
ID=11610997
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58005431A Granted JPS58190900A (en) | 1983-01-17 | 1983-01-17 | Production of quartz crystal |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58190900A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2153848C (en) * | 1994-07-18 | 2003-05-13 | Motoyuki Tanaka | Oxide thin film having quartz crystal structure and process for producing the same |
-
1983
- 1983-01-17 JP JP58005431A patent/JPS58190900A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58190900A (en) | 1983-11-07 |
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