JP3793794B2 - Ocean sand drift test sand - Google Patents
Ocean sand drift test sand Download PDFInfo
- Publication number
- JP3793794B2 JP3793794B2 JP2001403197A JP2001403197A JP3793794B2 JP 3793794 B2 JP3793794 B2 JP 3793794B2 JP 2001403197 A JP2001403197 A JP 2001403197A JP 2001403197 A JP2001403197 A JP 2001403197A JP 3793794 B2 JP3793794 B2 JP 3793794B2
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- JP
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- Prior art keywords
- sand
- glass
- test
- specific gravity
- drift
- 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.)
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- 239000004576 sand Substances 0.000 title claims description 66
- 239000011521 glass Substances 0.000 claims description 28
- 230000005484 gravity Effects 0.000 claims description 12
- 238000011835 investigation Methods 0.000 claims description 10
- 239000002699 waste material Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 6
- 239000004973 liquid crystal related substance Substances 0.000 claims description 3
- 239000006063 cullet Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000003973 paint Substances 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 150000002736 metal compounds Chemical class 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 238000007873 sieving Methods 0.000 description 3
- 239000005361 soda-lime glass Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LBFUKZWYPLNNJC-UHFFFAOYSA-N cobalt(ii,iii) oxide Chemical compound [Co]=O.O=[Co]O[Co]=O LBFUKZWYPLNNJC-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 150000001622 bismuth compounds Chemical class 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229910001429 cobalt ion Inorganic materials 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000002611 lead compounds Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000010309 melting process Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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- Sampling And Sample Adjustment (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は、海洋調査で用いられる漂砂調査用試験砂に関するものである
【0002】
【従来の技術】
海洋調査において、最も重要な調査の一つとして漂砂調査がある。この調査は、漂砂調査用試験砂を移動基点としたい定点に定量置設し、定点周辺にメッシュ状に調査点を設け、時間経過とともに各調査点で底質の定量採取を行い移動基点からの砂の移動状況(漂砂状況)について解析を行うものである。
【0003】
これまで調査用試験砂は、調査海域の砂を採取し、この砂に蛍光塗料を塗布して蛍光砂を製造していた。これは、採取した試料中に蛍光砂がどの程度含まれるかをブラックライト(紫外線)下で計数することにより、移動量を測定するためである。
【0004】
【発明が解決しようとする課題】
上記の蛍光砂を製造する方法には、以下のような種々の問題点が指摘されている。現地砂の採取、洗浄、乾燥、篩い分けや蛍光塗料の塗布、乾燥、粉砕、篩い分けという煩雑な作業が必要となり、製造時間やコストがかかりすぎる。また、屋内外の広い作業場が必要となる。均一な蛍光砂を製造するためには熟達した経験が必要となる。
【0005】
また、試験砂としては、以下の問題点が指摘されている。漂砂調査に伴う蛍光砂の追跡期間は、通常3時間後から3ヶ月後までであるが、海底に置設された蛍光砂は移動時の摩耗により蛍光塗料が徐々に削除されて、時間経過とともに試験砂としての均一性が低下してしまう。分析時に試料砂の蛍光塗料が剥落しているため、蛍光塗料の薄くなったものは識別しにくく、完落したものはカウント出来ないなど的確なデータが得られない。現地砂以外の素材で試験砂を製造する場合、現地砂と同じ粒径や比重のものを製造するのが非常に難しい。
【0006】
【課題を解決するための手段】
本発明は前記の課題を解決するために、全国で大量に排出され、新たな用途開発が求められている廃ガラスに着目し、それらのカレットを原料とする事により、製造工程が簡単で分析時の識別が容易な漂砂調査用試験砂を提供するに至った。
【0007】
【発明の実施の形態】
海砂の比重は2.7〜2.8であるのに対して、市中から排出される廃ガラスの大部分を占め、一般にソーダ石灰ガラスと呼ばれているびんガラスの比重は2.5前後であり、このままでは、試験砂として使用することはできない。
【0008】
そこで、海砂と同程度の比重を得るため、一般のソーダ石灰ガラスより密度の大きな金属化合物をガラスに添加するという結論に至った。そのための金属化合物としては、数多くあるが、鉛化合物のような環境に影響を及ぼす物質の使用は、好ましくない。また、鉛代替物質として脚光を浴びているビスマス化合物は、高価である。その中では、酸化亜鉛が、無色であり、価格が安く、毒性も無く、ガラス原料としてすでに使われていることから、最も好ましい物質の一つといえる。
【0009】
また、廃ガラスとしては一般のソーダ石灰ガラスの他、テレビのブラウン管ガラス、パソコンなどに使われる液晶ガラスのように電気用ガラスと呼ばれているものがある。ブラウン管ガラスのうち、パネルガラスと呼ばれている前面部の鉛を含まないガラスや液晶ガラスは、比重2.7〜2.8の海砂と同比重であり、試験砂の原料として十分使用できる。
【0010】
ここでいう電気用ガラスとは、ガラスの事典(作花済夫編、朝倉書店発行、1985年初版)126頁に記述されている電気・電子工業で用いられているバルブガラス、板ガラスの総称である。
【0011】
海砂の粒径は、JIS A 1204土の粒度試験によるとほぼ0.075〜2.0mmの範囲にあるが、ガラス素材であれば従来の水出し法による工程で数mm以下の粒状となるため、ボールミル型粉砕器などで海砂の粒径まで簡単に粉砕できる。その後、篩い分けすることによって、任意の粒径のガラス粉を抽出することができる。
【0013】
自然界における海砂には多種多様な鉱物等が含まれているため、様々な色調を有する砂粒が存在する。その中にあって、一般的には、青系の色調を持つ砂粒は非常にまれである。
【0014】
この点に着目して、本発明のガラス砂に、例えば、青色のカレットを使用したり、あるいは溶融工程で青色の色調を帯びる着色剤を添加することによって、分析の際、目視あるいは実態顕微鏡による検鏡での識別を容易にすることが可能となる。
【0015】
また、この方法は、従来の蛍光塗料を塗布する方法に比べて、着色剤がガラスの中に溶け込んでいるため、塗料の剥落などの影響が小さくなり、分析精度の向上が図られる。
【0016】
前記着色剤として、青系の場合、鉄、コバルト、銅などの化合物を単独又は、他の化合物と組み合わせてガラス中に溶解させる手法が一般的である。
【0017】
なかでも、コバルトイオンによる呈色が、微量で、溶融条件に左右されずに、鮮明な青色を作ることから、本発明には好ましい。
【0018】
ただし、海砂の色調と区別が可能な色調を得るために、前記青系着色剤に限らず、他の金属化合物を添加することも可能であるのは、自明である。
【0019】
自然界における海砂は、長期間の摩耗によって角のない丸みをおびた形状となっている。これに対してガラス砂は、角張った形状をしているため目視あるいは実態顕微鏡による検鏡によって識別が容易である。
【0020】
【実施例】
以下に本発明による海洋漂砂調査用試験砂の実施例及び比較例について記載する。以下の実施例は本発明の形態や効果についての理解を深めるためのものであり、本発明を制限するものではない。
【0021】
【実施例1】
廃ガラスの青色カレット100部と酸化亜鉛粉末20部をるつぼに秤量し、電気炉内で昇温速度150℃/hで1400℃まで昇温した。溶融したカレットを水中で急冷し、乾燥後、0.075〜2.0mmに篩い分けし、参考写真1にあるような漂砂調査用試験砂を得た。得られた試験砂の真比重は2.71であり、参考写真2にあるように肉眼でも海砂との識別は容易であった。
【0022】
【実施例2】
ブラウン管から採取したパネルガラスのカレット100部及び酸化コバルト粉末0.2部をるつぼに秤量し、電気炉で1400℃、1時間溶融後、水中で急冷し、青色カレットを得た。このカレットを乾燥後、0.075〜2.0mmにふるい分けし、実施例1の参考写真1と同様な漂砂調査用試験砂を得た。得られた試験砂の真比重は2.70であり、実施例1の参考写真2と同様に、肉眼でも海砂との識別は容易であった。
【0023】
【実施例3】
廃ガラスの無色カレット100部に酸化コバルト0.2部及び酸化亜鉛20部を加え、るつぼに秤量し、実施例1と同様の手法で、漂砂調査用試験砂を得た。得られた試験砂の真比重は2.72であり、実施例1の参考写真2と同様に、肉眼でも海砂との識別は容易であった。
【0024】
【比較例】
廃ガラスの無色カレット100部と酸化コバルト粉末0.2部をるつぼに秤量し、実施例1と同様の手法で、漂砂調査用試験砂を得た。得られた試験砂は、海砂との識別は容易であったが、真比重は2.50であり.、試験砂としての条件を満たさなかった。
【0025】
【発明の効果】
以上詳述したように、本発明は、廃ガラスと金属化合物を用いることで、従来の方法ではできなかった製造工程が簡単でかつ分析時の識別が容易な海洋漂砂調査用試験砂を得ることが可能になった。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to test sand for sand drift survey used in ocean surveys.
[Prior art]
One of the most important surveys in the ocean survey is the sand drift survey. In this survey, a fixed amount of test sand for sand drift survey is placed at a fixed point to be used as a moving base point, mesh points are set around the fixed point, and the sediment is quantitatively collected at each survey point over time. It analyzes the sand movement situation (sand drift situation).
[0003]
Until now, the sand for investigation was collected from the investigation sea area, and fluorescent sand was applied to this sand to produce fluorescent sand. This is to measure the amount of movement by counting how much fluorescent sand is contained in the collected sample under black light (ultraviolet light).
[0004]
[Problems to be solved by the invention]
The following various problems have been pointed out in the above method for producing fluorescent sand. Intricate operations such as sampling, washing, drying, sieving and application of fluorescent paint, drying, pulverization, and sieving are required, and production time and cost are too high. In addition, a large work place indoors and outdoors is required. Proven experience is required to produce uniform fluorescent sand.
[0005]
The following problems have been pointed out as test sand. The tracking period of the fluorescent sand accompanying the sand drift survey is usually from 3 hours to 3 months later. However, the fluorescent paint placed on the seabed is gradually removed due to wear during movement, and as time passes, Uniformity as test sand is reduced. Since the fluorescent paint of the sample sand is peeled off at the time of analysis, it is difficult to identify the thin fluorescent paint, and accurate data cannot be obtained, such as the complete one cannot be counted. When manufacturing test sand with materials other than local sand, it is very difficult to manufacture the same particle size and specific gravity as local sand.
[0006]
[Means for Solving the Problems]
In order to solve the above-mentioned problems, the present invention focuses on waste glass that is discharged in large quantities throughout the country and is required to develop new applications. By using those cullet as a raw material, the manufacturing process is simple and analyzed. We have provided test sand for sand drift investigation that allows easy identification of time.
[0007]
DETAILED DESCRIPTION OF THE INVENTION
While the specific gravity of sea sand is 2.7 to 2.8, it occupies most of the waste glass discharged from the city, and the specific gravity of bottle glass generally called soda lime glass is 2.5. It is around and cannot be used as test sand.
[0008]
In order to obtain a specific gravity similar to that of sea sand, a conclusion was reached that a metal compound having a density higher than that of general soda-lime glass is added to the glass. There are many metal compounds for this purpose, but it is not preferable to use substances that affect the environment, such as lead compounds. In addition, bismuth compounds that are in the spotlight as lead substitutes are expensive. Among them, zinc oxide is one of the most preferable materials because it is colorless, inexpensive, non-toxic and already used as a glass raw material.
[0009]
In addition to general soda-lime glass, waste glass includes what is called electrical glass, such as television CRT glass and liquid crystal glass used in personal computers. Among CRT glass, glass and liquid crystal glass that do not contain lead in the front part called panel glass have the same specific gravity as sea sand with a specific gravity of 2.7 to 2.8, and can be used sufficiently as a raw material for test sand. .
[0010]
Glass for electrical use here is a generic term for bulb glass and plate glass used in the electrical and electronic industry described in page 126 of the encyclopedia of glass (Sakuo Sakuo, Asakura Shoten, first published in 1985). is there.
[0011]
The particle size of sea sand is in the range of about 0.075 to 2.0 mm according to the particle size test of JIS A 1204 soil. Therefore, the particle size of sea sand can be easily pulverized with a ball mill type pulverizer. Thereafter, glass powder having an arbitrary particle size can be extracted by sieving.
[0013]
Since sea sand in nature contains a wide variety of minerals, sand grains having various colors exist. Among them, in general, sand grains having a blue color tone are very rare.
[0014]
Focusing on this point, the glass sand of the present invention, for example, by using a blue cullet or by adding a colorant having a blue color tone in the melting process, in the case of analysis, by visual observation or by actual microscope Identification with a speculum can be facilitated.
[0015]
Further, in this method, since the colorant is dissolved in the glass as compared with the conventional method of applying the fluorescent paint, the influence of the peeling of the paint is reduced, and the analysis accuracy is improved.
[0016]
As the colorant, in the case of a blue system, a method of dissolving a compound such as iron, cobalt, or copper alone or in combination with another compound in glass is common.
[0017]
Among them, the coloration by cobalt ions is preferable for the present invention because it produces a very clear blue color regardless of the melting conditions.
[0018]
However, in order to obtain a color tone that can be distinguished from the color tone of sea sand, it is obvious that other metal compounds can be added in addition to the blue-based colorant.
[0019]
Sea sand in nature has a rounded shape with no corners due to long-term wear. On the other hand, since glass sand has an angular shape, it can be easily identified by visual inspection or inspection with an actual microscope.
[0020]
【Example】
Examples and comparative examples of ocean sand drift test sand according to the present invention will be described below. The following examples are for deepening the understanding of the form and effect of the present invention, and do not limit the present invention.
[0021]
[Example 1]
100 parts of blue cullet of waste glass and 20 parts of zinc oxide powder were weighed in a crucible and heated to 1400 ° C. at a heating rate of 150 ° C./h in an electric furnace. The melted cullet was quenched in water, dried, and sieved to 0.075 to 2.0 mm to obtain test sand for sand drift investigation as shown in Reference Photo 1. The true specific gravity of the obtained test sand was 2.71, and as shown in Reference Photo 2, it was easy to distinguish it from sea sand with the naked eye.
[0022]
[Example 2]
100 parts of panel glass cullet and 0.2 parts of cobalt oxide powder collected from the cathode ray tube were weighed in a crucible, melted at 1400 ° C. for 1 hour in an electric furnace, and then rapidly cooled in water to obtain a blue cullet. After drying this cullet, it was sieved to 0.075 to 2.0 mm to obtain the test sand for sand drift investigation similar to Reference Photo 1 of Example 1. The true specific gravity of the obtained test sand was 2.70, and as in Reference Photo 2 of Example 1, it was easy to distinguish it from sea sand with the naked eye.
[0023]
[Example 3]
Cobalt oxide 0.2 part and zinc oxide 20 part were added to 100 parts of colorless cullet of waste glass, and weighed in a crucible, and the test sand for sand drift investigation was obtained in the same manner as in Example 1. The true specific gravity of the obtained test sand was 2.72, and as in Reference Photo 2 of Example 1, it was easy to distinguish it from sea sand with the naked eye.
[0024]
[Comparative example]
100 parts of colorless cullet of waste glass and 0.2 part of cobalt oxide powder were weighed in a crucible, and test sand for sand drift investigation was obtained in the same manner as in Example 1. The obtained test sand was easy to distinguish from sea sand, but the true specific gravity was 2.50. The condition as test sand was not satisfied.
[0025]
【The invention's effect】
As described in detail above, the present invention obtains test sand for marine drift sand investigation that uses a waste glass and a metal compound, which is simple in the manufacturing process that could not be performed by the conventional method and easy to identify during analysis. Became possible.
Claims (2)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001403197A JP3793794B2 (en) | 2001-12-27 | 2001-12-27 | Ocean sand drift test sand |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001403197A JP3793794B2 (en) | 2001-12-27 | 2001-12-27 | Ocean sand drift test sand |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003194843A JP2003194843A (en) | 2003-07-09 |
| JP3793794B2 true JP3793794B2 (en) | 2006-07-05 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001403197A Expired - Fee Related JP3793794B2 (en) | 2001-12-27 | 2001-12-27 | Ocean sand drift test sand |
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| Country | Link |
|---|---|
| JP (1) | JP3793794B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4580245B2 (en) * | 2005-01-14 | 2010-11-10 | 株式会社パスコ | Drift sand flow analysis system and drift sand flow analysis method |
-
2001
- 2001-12-27 JP JP2001403197A patent/JP3793794B2/en not_active Expired - Fee Related
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| Publication number | Publication date |
|---|---|
| JP2003194843A (en) | 2003-07-09 |
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