JPS6329247Y2 - - Google Patents

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Publication number
JPS6329247Y2
JPS6329247Y2 JP5623782U JP5623782U JPS6329247Y2 JP S6329247 Y2 JPS6329247 Y2 JP S6329247Y2 JP 5623782 U JP5623782 U JP 5623782U JP 5623782 U JP5623782 U JP 5623782U JP S6329247 Y2 JPS6329247 Y2 JP S6329247Y2
Authority
JP
Japan
Prior art keywords
filter
water
particles
homogenizer
polluted water
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
Application number
JP5623782U
Other languages
Japanese (ja)
Other versions
JPS58158345U (en
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to JP5623782U priority Critical patent/JPS58158345U/en
Publication of JPS58158345U publication Critical patent/JPS58158345U/en
Application granted granted Critical
Publication of JPS6329247Y2 publication Critical patent/JPS6329247Y2/ja
Granted legal-status Critical Current

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  • Investigating Or Analysing Biological Materials (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Disintegrating Or Milling (AREA)

Description

【考案の詳細な説明】 本考案は、分析などの計測に先立つて汚濁水を
前処理する装置に関する。
[Detailed Description of the Invention] The present invention relates to an apparatus for pre-treating polluted water prior to measurement such as analysis.

河川水、湖沼水など油滴、動植物の遺体細ない
し菌類、藻類などの微生物(以下微生物で代表せ
しむ)を浮遊物として含有する汚濁水を分析する
際には、通常、それら浮遊物を去したものにつ
いて分析が行なわれる。分析成分として窒素N、
燐P、化学的酸素要求量COD、水素イオン濃度
指数PHなどが要求されている場合には、前記分析
の結果は、多くの場合満足な結果を与えない。と
いうのはそれら微生物の細胞内容物の含有する窒
素、燐など分析要素が、菌体の去と同時に除却
されているからである。したがつて、正確な分析
値を得ようとするならば、分析などの計測に先立
つて微生物の細胞膜を破壊するための前処理が必
要となる。
When analyzing polluted water such as river water, lake water, etc. that contains oil droplets, remains of animals and plants, or microorganisms such as fungi and algae (hereinafter referred to as microorganisms) as suspended matter, these suspended matter are usually removed. An analysis will be conducted on what has been done. Nitrogen N as an analysis component,
When phosphorus P, chemical oxygen demand COD, hydrogen ion concentration index PH, etc. are required, the results of said analysis often do not give satisfactory results. This is because analytical elements such as nitrogen and phosphorus contained in the cell contents of these microorganisms are removed at the same time as the bacterial cells are removed. Therefore, in order to obtain accurate analysis values, pretreatment to destroy the cell membranes of microorganisms is required prior to analysis or other measurements.

本考案は、上述した前処理のための装置であつ
て、いまこれ実施例たる図面につき説明する。本
考案装置の部分である過器1は、床1aによ
つて、上側の被検液8たる汚濁水の収容部1bと
下側の脚部1dとに2分せられている容器状体で
あり、収容部1bの上部には、管路状の開口1c
が設けられ、脚部1dは漏斗状をしていて、その
脚端は管路4を介して洗浄用管路4a、計測器用
管4bに接続されている。
The present invention is an apparatus for the above-mentioned pretreatment, and will now be described with reference to the drawings, which are embodiments thereof. The filter vessel 1, which is a part of the device of the present invention, is a container-shaped body divided into two by a floor 1a into an upper container 1b for containing contaminated water, which is the sample liquid 8, and a lower leg 1d. There is a conduit-shaped opening 1c in the upper part of the housing part 1b.
The leg portion 1d is funnel-shaped, and the end of the leg is connected via a conduit 4 to a cleaning conduit 4a and a measuring instrument conduit 4b.

床1aは、その材にとくに限定はないが、
ガラスフイルタのような多孔質の板体で壁に固
定されており、その上面にはガラス粒子2群が載
せられる。このガラス粒子の大きさは、実使用の
結果4〜20メツシユ程度のものが適当とされる。
The material for the floor 1a is not particularly limited, but
It is fixed to the wall with a porous plate like a glass filter, and two groups of glass particles are placed on the top surface of the plate. As a result of practical use, the appropriate size of the glass particles is about 4 to 20 mesh.

本考案にあたつては、このような過器1に超
音波ホモジナイザ3が付設される。付設に当つて
は、その振動子3aの少なくとも先端部が収容部
に収容された被検液8の液面L下に位置するよう
になされねばならない。ここに液面L下に位置す
るようにというは、振動子3aの先端が固定的に
液面L下に入るようにした場合のほか、図示しな
いがホモジナイザ自体を位置移動させて、液面L
下に入ることを可能ならしめた場合を含む。ホモ
ジナイザ3が付設される理由は、むろん、その稼
動の際の強烈な撹拌力ないし剪断力によつて、被
検汚濁水中に浮遊している微生物の細胞を破壊
し、細胞液を被検液中に取出して一体に溶液化す
るためである。これがため付設されるホモジナイ
ザ3の消費電力は、本考案者が実験的に求めたと
ころによれば、30W〜300Wで足る。
In the present invention, an ultrasonic homogenizer 3 is attached to such a filter 1. When installing the vibrator 3a, at least the tip of the vibrator 3a must be positioned below the liquid level L of the test liquid 8 contained in the storage portion. Here, being positioned below the liquid level L means that the tip of the vibrator 3a is fixedly positioned below the liquid level L, or by moving the homogenizer itself (not shown) to lower the liquid level L.
This includes cases where it is possible to enter the area below. The reason why the homogenizer 3 is attached is, of course, that the intense stirring or shearing force generated during operation of the homogenizer destroys the cells of microorganisms floating in the contaminated water to be tested, and the cell fluid is released into the test liquid. This is to take it out and turn it into a solution. Therefore, the power consumption of the attached homogenizer 3 is 30W to 300W, according to what the present inventor has determined experimentally.

前述した過器脚部1dの脚端に接続されてい
る計測用管路4bには、真空ポンプ6が介在さ
れ、この真空ポンプ6によつて被検液の過を促
すととともに液を計測器7に送給する。洗浄用
管路4aにはバルブ5を介して洗浄水源W1に接
続されている。
A vacuum pump 6 is interposed in the measuring conduit 4b connected to the leg end of the measuring device leg 1d, and the vacuum pump 6 accelerates the flow of the test liquid and transfers the liquid to the measuring device. 7. The cleaning pipe 4a is connected to a cleaning water source W1 via a valve 5.

上述した本考案装置を使用するに当つては、被
検汚濁液8の所定量、例えば100mlを、収容部1
b内に入れ、ポンプ6およびホモジナイザ3をた
とえば1分間稼動して、減圧過を促し、かつ微
生物細胞を破壊させる。したがつて、その液に
よる分析結果は、窒素、燐、化学的酸素要求量、
水素イオン濃度指数などについて、正しい値を与
える。このような過によつてガラス粒子2群上
には、逐次破壊された細胞膜残渣その他浮遊物が
蓄積する。そのような場合には、バルブ5を開い
て洗浄水W1を管路4aを経て過器1内に逆流
させる。このとき、ガラス粒子2は過器1内で
舞い上がり、ガラス粒子2に付着された細胞膜残
渣などが除去される。その後、開口1cから洗浄
廃水W2を溢流除去させるものである。
When using the device of the present invention described above, a predetermined amount of the polluted liquid 8 to be tested, for example 100 ml, is placed in the container 1.
b, and the pump 6 and homogenizer 3 are operated for, for example, 1 minute to promote vacuum and destroy microbial cells. Therefore, the analysis results for the liquid include nitrogen, phosphorus, chemical oxygen demand,
Give correct values for hydrogen ion concentration index, etc. As a result of this process, residues of cell membranes and other floating substances that have been sequentially destroyed accumulate on the second group of glass particles. In such a case, the valve 5 is opened to allow the wash water W1 to flow back into the filter 1 through the pipe 4a. At this time, the glass particles 2 fly up in the strainer 1, and cell membrane residues and the like attached to the glass particles 2 are removed. Thereafter, the cleaning waste water W2 is allowed to overflow and be removed from the opening 1c.

したがつて、本考案装置によれば、正しい計測
よう汚濁水が迅速に前処理できるのである。
Therefore, according to the device of the present invention, polluted water can be quickly pretreated for accurate measurements.

【図面の簡単な説明】[Brief explanation of the drawing]

図面は本考案装置の模式的な説明図である。 1……過器、1a……床、1b……被検汚
濁水収容部、1c……開口部、1d……脚部、2
……ガラス粒子、3……ホモジナイザ、3a……
振動子、4……管路、4a……洗浄用管路、4b
……計測器用管路、5……バルブ、6……真空ポ
ンプ、7……計測器、8……被検汚濁水。
The drawing is a schematic explanatory diagram of the device of the present invention. 1...Separator, 1a...Floor, 1b...Test contaminated water storage section, 1c...Opening, 1d...Legs, 2
...Glass particles, 3...Homogenizer, 3a...
Vibrator, 4... Conduit, 4a... Cleaning conduit, 4b
...Measuring instrument pipe, 5...Valve, 6...Vacuum pump, 7...Measuring instrument, 8...Test polluted water.

Claims (1)

【実用新案登録請求の範囲】 (1) 床1a上に粒子2群を載置した過器1
は、超音波ホモジナイザ3をその振動子3aが
前記過器収容部1b内に収容した被検液面L
下に入り、または入ることのできる位置に付設
しており、かつ前記過器脚部1dが水洗用管
路4aに接続していることを特徴とする汚濁水
の計測前処理装置。 (2) 粒子2は、その大きさが4〜20メツシユのガ
ラス粒子であることを特徴とする実用新案登録
請求の範囲第1項記載の汚濁水の計測前処理装
置。
[Claims for Utility Model Registration] (1) Filter vessel 1 with two groups of particles placed on bed 1a
is the liquid level L to be tested in which the ultrasonic homogenizer 3 and its vibrator 3a are housed in the filter housing section 1b.
A pretreatment device for measurement of polluted water, characterized in that it is attached to a position where it can be inserted or entered, and the filter leg portion 1d is connected to a water washing pipe 4a. (2) The polluted water measurement pre-treatment device according to claim 1, wherein the particles 2 are glass particles having a size of 4 to 20 mesh.
JP5623782U 1982-04-16 1982-04-16 Polluted water measurement pre-treatment device Granted JPS58158345U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5623782U JPS58158345U (en) 1982-04-16 1982-04-16 Polluted water measurement pre-treatment device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5623782U JPS58158345U (en) 1982-04-16 1982-04-16 Polluted water measurement pre-treatment device

Publications (2)

Publication Number Publication Date
JPS58158345U JPS58158345U (en) 1983-10-22
JPS6329247Y2 true JPS6329247Y2 (en) 1988-08-05

Family

ID=30066775

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5623782U Granted JPS58158345U (en) 1982-04-16 1982-04-16 Polluted water measurement pre-treatment device

Country Status (1)

Country Link
JP (1) JPS58158345U (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003144149A (en) * 1997-03-31 2003-05-20 Takara Holdings Inc Isolation apparatus and method of using the same
JP5663311B2 (en) 2008-01-09 2015-02-04 ケック グラデュエイト インスティテュート Substance adjustment and / or handling systems, devices and methods
WO2010151705A2 (en) 2009-06-26 2010-12-29 Claremont Biosolutions Llc Capture and elution of bio-analytes via beads that are used to disrupt specimens

Also Published As

Publication number Publication date
JPS58158345U (en) 1983-10-22

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