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JPH0521184B2 - - Google Patents
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JPH0521184B2 - - Google Patents

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Publication number
JPH0521184B2
JPH0521184B2 JP58005216A JP521683A JPH0521184B2 JP H0521184 B2 JPH0521184 B2 JP H0521184B2 JP 58005216 A JP58005216 A JP 58005216A JP 521683 A JP521683 A JP 521683A JP H0521184 B2 JPH0521184 B2 JP H0521184B2
Authority
JP
Japan
Prior art keywords
fine aggregate
water
centrifugal force
moisture
measuring
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 - Lifetime
Application number
JP58005216A
Other languages
Japanese (ja)
Other versions
JPS59131164A (en
Inventor
Yasuro Ito
Yoshiro Higuchi
Takeshi Shiki
Yukikazu Tsuji
Masaaki Tsuji
Mitsutaka Hayakawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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 by Individual filed Critical Individual
Priority to JP521683A priority Critical patent/JPS59131164A/en
Priority to US06/882,034 priority patent/US4715719A/en
Priority to PCT/JP1984/000008 priority patent/WO1984002872A1/en
Publication of JPS59131164A publication Critical patent/JPS59131164A/en
Priority to US06/788,227 priority patent/US4686852A/en
Publication of JPH0521184B2 publication Critical patent/JPH0521184B2/ja
Granted legal-status Critical Current

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Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/38Concrete; Lime; Mortar; Gypsum; Bricks; Ceramics; Glass

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Ceramic Engineering (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Measuring Volume Flow (AREA)
  • Preparation Of Clay, And Manufacture Of Mixtures Containing Clay Or Cement (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は細骨材の含水率測定方法および装置の
創案に係り、セメント又は石膏のような水硬性物
質粉体に配合してモルタル又はコンクリートのよ
うな混練物を調整するに当つて不可欠の素材であ
る砂のような細骨材に関して、その配合混練に際
し合理的な水量を決定するための含水率を短時間
内に的確に測定し得る方法に関する。セメントの
ような水硬性物質粉体に細骨材(及び粗骨材、繊
維材その他の助剤ないし添加剤)と配合水を添加
混合してモルタル又はコンクリートのような生混
練物を調整することは従来から広く実施されてい
るところであるが、このようにして調整された生
混練物ないし該生混練物を成形硬化せしめて得ら
れる各種製品の品質特性にはそれなりのバラツキ
が避け得ないことも周知の通りである。特に本発
明者等の開発した造殻混練(分割練り混ぜ)方法
による場合においては1次水量(或いはその後2
次水量)を的確に決定することが必要で、その如
何により品質特性に影響するところが大きい。こ
れは前記したような細骨材に吸着ないし附着され
あ水量を的確に把握し得ないことによるものであ
つて、事実屋外に山積みされた砂に吸着ないし附
着した水量は多様に変動することは実地的に明か
なところであり、このように水量を異にした砂を
用いた場合においては前記した品質ないし特性に
大きな変動を来さざるを得ない。 ところで、このような細骨材に関しては
JISA1109の「細骨材の比重及び吸水率試験方法)
が規定されており、即ち所定のフローコーン内に
試料を規定手法で充填したものを、台上に転倒状
態として置き、前記フローコーンを引き上げたと
きに細骨材がはじめてスランプしたときを表面乾
燥飽水状態(Saturated surface−dry
condition)であるとするもので、この状態にお
ける細骨材含有水分は細骨材内部の空隙が水で満
たされ(飽水)、しかも表面は水のない乾燥状態
であるとされ、従つて前記したような生混練物の
調整に当つては前記試験によつて得られた含水率
を以て該細骨材自体の非有効水率となし、このよ
うな細骨材の水分は配合に関与しないものとして
配合水決定に際して除外したものを基準値として
いる。ところがこのようなJIS規定の表面乾燥状
態の細骨材について本発明者等が検討した結果、
上記のように非有効水と考えることは不合理であ
るとの結論に達した。 即ち本発明者等は大井川産のC砂、E砂および
砕砂を用い、真空ミキサーを用いて砂表面に空気
分を残留させないように730mmHgの減圧下でそれ
ぞれ水と混合し、所定の含水率となるように試料
を作成し、これをアクリル容器に所定の正確な状
態で充填すると共にフロー試験テーブル上に置い
て15回上下作動して締固めたものについて重量を
測定した後、含水率と空隙率(絶対乾燥状態で)
を求め、これらの測定結果を要約して示すと共に
それらの細骨材についてのJIS規定による前記表
面乾燥飽水状態(以下表乾燥状態という)の含水
率をも示すと第1図に示す通りである。蓋しこの
第1図によると前記したような各細骨材におい
て、前記表乾燥状態以下であつても含水率の変動
によつてバルキング(空隙率)の変化が明かに示
されるものであり、又これとは別に節分けされた
細骨材に対する吸水率変化による粒径の影響、或
いは遠心力試験などによつてこれに準じた結果が
認められ、何れにしても前記JIS規定による表面
乾燥飽水状態Qにおいてはなお骨材表面にそれな
りの骨材に拘束された限界表面吸着水率
(SWlim)を有するものと言わざるを得ない。即
ち前記表面乾燥飽水状態Qは内部飽水率Q0と前
記固有表面吸着水(SWlim)との和Q=Q0
SWlimであつて、真の非有効水は前記Q0のみで
あることを確認し、これを非有効水の基準値とす
べきである。 ところで上記したような表面乾燥飽水状態Q、
内部飽水率Q0、固有表面吸着水SWlimの如きを
求めるにはそれらの測定をなし、少くともQ値を
求めることがベースであるが、従来このような表
面乾燥飽水状態Qを求める適切な手法がなく、即
ち例えば前記細骨材を密閉容器中に収容して長時
間(例えば1カ月前後の如し)保持することによ
つて該状態を形成し得るとしてもこのような長時
間を必要としたのでは1つの測定値を得るために
月単位の期間が消費され、量産的に大量に消費さ
れ、必然的に多品種とならざるを得ない細骨材
(砂)についてその需要条件に即した測定結果を
求め得ない。なお本発明者等は上記のような細骨
材については前記したSWlimとは別に最大表面
吸着水率SWmaxと称すべきものを確認してお
り、これらの関係を比較的短時間内に解明するこ
とが枢要である。 本発明はこのような実情に鑑み検討を重ねて創
案されたものであつて、このために適切に湿潤化
された細骨材を密閉容器内に収容したものを遠心
力作用機構によつて処理し、しかも分離された水
に関してはこれを細骨材と区分し、遠心力の作用
条件下たるとその停止条件たるとを問わず、適切
に管理し再び細骨材に吸着ない附着されることが
ないように保持するものである。 蓋しこのような構想に基いてこれを具体的に実
現するように本発明者等が設計、使用した遠心力
利用による細骨材の水分分離試験装置の詳細につ
いては第2図に示すように5mmφの塩化ビニル管
10の一端にアクリル板11を取付けた高さ10cm
の第1筒体と同一寸法で高さ5mmの第2の筒体1
0との間に0.15mmの金属線による金網12と濾紙
13および厚さ1.6mmの孔あき打抜き鉄板14と
を介装し、第1筒体に試料細骨材を200g宛充填
すると共に第2筒体10には脱脂綿16を充填し
たものを第3図のように対向させてビニルテープ
15を周面に接着することにより一体化すると共
に密閉したものを第4図に示すように蓋21を施
すようにされたケース20内の回転板22に軸2
5を以て傾動可能に設けられた受器24内に半量
以上を収容させ、この状態で回転板22を回転さ
せることによつて所定の遠心力を作用させるよう
にしたものであつて、第1筒体からの分離排出水
は第2筒体の脱脂綿16に吸収され、しかも試験
のための回転板22の回動停止時にこのように脱
脂綿16に吸収された水分が逆流しないように成
つているものである。 なお上記のように管体10,10をビニルテー
プ15の如きで密閉することは本発明において前
記したような限界表面吸着水率SWlimや表面乾
燥飽水状態における内部飽水率Q0を求める上に
おいて枢要であつて、単に蓋を施して試験材を装
入した容器を用いて遠心力作用せしめた場合にお
いてはその遠心力作用条件において容器内空気が
外部に放出され、一般的には容器内が減圧化され
且つ容器の内外間における空気の変換流動が繰返
されることとなり、このような容器内外間におけ
る空気の変換流動によつて水分も気散排出される
こととなり、その減圧条件によつても水分気散が
増加することとなる。このような空気の流動変換
に伴う水分の気散排出を適当に防止して遠心力を
作用せしめ、測定結果を得ることが必要であつ
て、このため前記密閉状態の形成は重要と言え
る。 然して上記したような装置により1例として大
井川産E砂(FM=3.23で、空隙率ε=33.8%)
に関し前記JISA1109により測定されたQ値は
1.39%であるが、このものについて附着水量を、
一旦110℃の温度で24時間乾燥させた絶乾状態の
ものとしてその重量を測定し、その後に−730mm
Hgの真空ミキサー内で、1Qから10Qの範囲で
種々に変化せしめたものを準備し、これらのもの
を120分間に亘つて453g(gは重力加速度)の遠
心力を作用させ、水分の分離処理した結果を要約
して横軸(処理時間)を対数目盛として示すと第
5図に示す通りである。 即ちこの第5図の結果によると、4Q以下の含
水率のものは遠心力作用時間に比例して整然とし
て含水率が低下し、1Qのものでは殆んど含水率
の低下がない。これに対しそれ以上のものにおい
ては最初の5分以内において急速に低下するがそ
の後は緩漫な低下となり、少くとも5分以降にお
いては4Q以下のものにおける含水率低下状態と
殆んど差のない含水率低下挙動を示している。即
ちこの横対数グラフ上変曲点があり、これら最大
表面吸着水率SWmaxと認められ、この変曲点で
ある最大表面吸着水率以上に附着された水分は比
較的容易に分離されるものであるのに対し、それ
以下のものは分離が緩漫化するものと言える。な
おこのような現象はその他の何れの砂において
も、その具体的数値は異ることになるとしても殆
んど同様に認められるものであつて、この第5図
のものとは別にFM=3.01で、空隙率ε=33.0%
の相模川砂は前記JISA1109によるQ値は3.12%
と第5図の場合よりは相当に高いものであるが、
このものについては全く同様の試験測定をなした
結果を同じに要約して示すと第6図の通りであ
る。即ちこの相模川砂の場合においては前記第5
図と同じ横軸対数グラフにおいて3Qまでは略直
線状に含水率が低下するのに対して4Q以上では
遠心力作用時間5分の位置で明確な変曲が認めら
れこの場合においては3Q前後において前記
SWmaxがあるものと認められる。 なお前記した各細骨材及びその他の代表的な5
種の細骨材について初期含水率をそれぞれ1Q前
後となるように調整したものについて同様の遠心
力分離試験を行つた結果を併せて示すと第7図の
如くであつて多少の変動が認められるとしても何
れの細骨材も分離処理時間の長短に拘わらず殆ん
ど変化のない状態であることが確認され、この結
果からすれば前記JISA1109による試験結果は含
水率として安定したものと言える。又前記したよ
うな試験測定に当つてその絶乾重量測定後におい
ては附着水の添加を上述したような減圧条件下に
実施することが枢要であつて、細骨材に水を添加
含有させるに当つて−730mmHgのような減圧条件
とすると、細骨材表面に附着している空気を実質
的有効に除去することができ、この状態で水を添
加混合すると添加した水が細骨材の組織中に有効
に滲透せしめられると共に附着した水分が安定且
つ一定化したものとなる。これに対し単に大気中
で加水混合したものは附着した水分が細骨材表面
において偏在している可能性が高く、従つて不安
定であつて測定結果が変動する。例えば前記大井
川E砂について絶乾状態とされたものに対し真空
ミキサー中で前記減圧条件で加水混合されたもの
と、大気中で混合加水したものを同じく遠心力分
離処理した結果は第8図の通りであつて、同じ処
理時間であつても測定結果が変化し、大気中で加
水混合したものは含水率が低いと共に相当のばら
つきがある。減圧条件を採用したものは反覆試験
した結果においても略安定し変動が殆んどないも
のであつて、同様の結果は前記相模川砂、水滓
砂、或いは標準砂の如きの何れの場合においても
確認され、従つて重量測定などのために絶乾状態
とされたものについては減圧条件下で加水混合
し、所定のQ値をもつたものとすることが正確な
測定結果を得る上において不可欠的であるが、例
えば24時間のようにそれなりに長時間に亘つて浸
水状態とされていたものにおいてはそのままで試
験測定しても同様に正確な結果が得られ(その後
に絶乾状態として重量を測定する)るもので、少
くとも細骨材におけ水との遭遇履歴を一定状態と
することが必要である。 更に上記したような遠心力分離について各種の
細骨材を検討した結果を説明すると、次の第1表
に示すような11種類の細骨材について夫々3Qに
相当した水分を附着含有させたものを準備し、こ
れらの細骨材を上記したところと同じ453gの重
力加速度による遠心力分離処理した結果は併せて
この第1表の下段において経過処理時間との関係
で示す通りである。
The present invention relates to the invention of a method and device for measuring the moisture content of fine aggregate, which is an indispensable material when mixed with hydraulic material powder such as cement or gypsum to prepare a kneaded material such as mortar or concrete. The present invention relates to a method for accurately measuring the moisture content of fine aggregate such as sand within a short period of time in order to determine a reasonable amount of water for mixing and kneading the fine aggregate. Adding and mixing fine aggregate (and coarse aggregate, fiber materials, and other auxiliaries or additives) and mixed water to hydraulic substance powder such as cement to prepare a ready-mixed material such as mortar or concrete. Although this has been widely practiced in the past, it is inevitable that there will be some variation in the quality characteristics of the green kneaded material prepared in this way or the various products obtained by molding and hardening the green kneaded material. As is well known. In particular, when using the shell kneading (divided kneading) method developed by the present inventors, the primary water amount (or the subsequent
It is necessary to accurately determine the amount of water used, and how it is determined will greatly affect the quality characteristics. This is due to the fact that the amount of water adsorbed to or attached to the fine aggregate cannot be accurately determined as described above, and in fact, the amount of water adsorbed to or attached to the sand piled outdoors varies widely. It is clear from a practical point of view that when sand with different amounts of water is used, the above-mentioned quality or characteristics inevitably vary greatly. By the way, regarding such fine aggregate,
JISA1109 “Specific gravity and water absorption test method of fine aggregate”
In other words, a sample is filled in a specified flow cone using a specified method, placed upside down on a table, and when the flow cone is pulled up, the time when the fine aggregate slumps for the first time is defined as surface drying. Saturated surface-dry
condition), and the moisture contained in the fine aggregate in this state is that the voids inside the fine aggregate are filled with water (saturated), and the surface is dry with no water. When preparing such a green kneaded product, the water content obtained in the above test is used as the ineffective water content of the fine aggregate itself, and the water content of such fine aggregate does not play a role in the blending. The standard value is that which is excluded when determining the blended water. However, as a result of the inventors' study of fine aggregate in a surface dry state as specified by JIS,
We have reached the conclusion that it is unreasonable to consider water as ineffective as described above. That is, the present inventors used C sand, E sand, and crushed sand from Oigawa River, and mixed them with water using a vacuum mixer under a reduced pressure of 730 mmHg so as not to leave any air on the sand surface, and then mixed them with water to a predetermined moisture content. A sample was prepared, filled into an acrylic container in the specified precise state, placed on a flow test table, and compacted by moving up and down 15 times. After measuring the weight, the moisture content and voids were determined. rate (in absolute dry condition)
Figure 1 summarizes these measurement results and also shows the moisture content in the surface dry saturated state (hereinafter referred to as surface dry state) for these fine aggregates according to JIS regulations. be. According to Fig. 1 of the cover, in each of the fine aggregates mentioned above, changes in bulking (porosity) are clearly shown due to changes in moisture content even if the condition is below the above-mentioned surface dry state. In addition, results similar to this have been found in the influence of particle size due to changes in water absorption of fine aggregates separated into sections, or in centrifugal force tests. In the water state Q, it must be said that the aggregate surface still has a certain limit surface adsorption water rate (SWlim) bound by the aggregate. That is, the surface dry water saturation state Q is the sum of the internal water saturation rate Q 0 and the intrinsic surface adsorption water (SWlim) Q = Q 0 +
It is SWlim, and it should be confirmed that the true non-effective water is only the Q 0 mentioned above, and this should be used as the standard value for the non-effective water. By the way, the surface dry saturated state Q as mentioned above,
In order to obtain the internal water saturation rate Q 0 and the specific surface adsorbed water SWlim, it is basic to measure them and find at least the Q value. For example, even if such a state could be created by storing the fine aggregate in a closed container and holding it for a long time (for example, about one month), it would be difficult to maintain the condition for such a long time. The demand conditions for fine aggregate (sand), which requires a period of months to obtain one measured value, is consumed in large quantities in mass production, and inevitably has to be produced in many different types. It is not possible to obtain measurement results that match the actual conditions. In addition, the present inventors have confirmed that for the above-mentioned fine aggregates, there is something that should be called the maximum surface adsorption water rate SWmax, in addition to the above-mentioned SWlim, and it is hoped that these relationships will be clarified within a relatively short period of time. is important. The present invention was devised after repeated studies in view of the above circumstances, and for this purpose, appropriately moistened fine aggregate stored in a closed container is processed by a centrifugal force mechanism. However, as for the separated water, it should be separated from the fine aggregate and should be properly managed to prevent it from being adsorbed or attached to the fine aggregate again, regardless of whether it is subjected to centrifugal force or stopped. It should be kept as such. The details of the water separation test device for fine aggregate using centrifugal force, which was designed and used by the inventors to specifically realize this idea based on this concept, are shown in Figure 2. 10 cm height with acrylic plate 11 attached to one end of 5 mmφ PVC pipe 10
A second cylindrical body 1 with the same dimensions as the first cylindrical body and a height of 5 mm.
A wire mesh 12 made of a metal wire of 0.15 mm, a filter paper 13, and a perforated punched iron plate 14 of 1.6 mm in thickness are interposed between the first cylindrical body and the second cylindrical body. The cylindrical body 10 is filled with absorbent cotton 16 and placed facing each other as shown in FIG. 3, and is integrated and sealed by adhering vinyl tape 15 to the circumferential surface, and then a lid 21 is attached as shown in FIG. The shaft 2 is attached to the rotary plate 22 in the case 20, which is
A predetermined centrifugal force is applied by rotating the rotary plate 22 in this state, and a predetermined centrifugal force is applied to the first cylinder. Water separated and discharged from the body is absorbed by the absorbent cotton 16 of the second cylindrical body, and the water absorbed by the absorbent cotton 16 is prevented from flowing back when the rotary plate 22 stops rotating for testing. It is. Note that sealing the pipe bodies 10, 10 with vinyl tape 15 as described above is useful for determining the critical surface adsorption water rate SWlim and the internal water saturation rate Q 0 in the surface dry saturated state as described above in the present invention. This is important, and when a centrifugal force is applied to a container filled with a test material with a lid, the air inside the container is released to the outside under the conditions of centrifugal force. is reduced in pressure and the conversion flow of air between the inside and outside of the container is repeated, and moisture is also diffused and discharged due to this conversion flow of air between the outside and outside of the container. This also results in increased moisture dissipation. It is necessary to appropriately prevent the vaporization and discharge of moisture associated with such air flow conversion and apply centrifugal force to obtain measurement results, and for this reason, the formation of the sealed state is important. However, as an example, E sand from Oigawa (FM = 3.23, porosity ε = 33.8%) was obtained using the above-mentioned device.
The Q value measured according to JISA1109 above is
The amount of water landing on this item is 1.39%.
Once dried at a temperature of 110℃ for 24 hours, its weight was measured, and then -730mm
In a Hg vacuum mixer, various samples with varying degrees of pressure ranging from 1Q to 10Q are prepared, and a centrifugal force of 453g (g is gravitational acceleration) is applied to these samples for 120 minutes to separate water. The results are summarized and shown in FIG. 5, with the horizontal axis (processing time) plotted on a logarithmic scale. That is, according to the results shown in Fig. 5, the water content of samples with a water content of 4Q or less decreases in an orderly manner in proportion to the centrifugal force action time, and the water content of samples with a moisture content of 1Q hardly decreases. On the other hand, in the case of water content higher than 4Q, the water content decreases rapidly within the first 5 minutes, but then it decreases slowly, and at least after 5 minutes, there is almost no difference between the moisture content and the water content of water content lower than 4Q. It shows no moisture content decreasing behavior. In other words, there is an inflection point on this horizontal logarithmic graph, which is recognized as the maximum surface adsorption water rate SWmax, and the water attached above this inflection point, which is the maximum surface adsorption water rate, is relatively easily separated. On the other hand, if it is less than that, it can be said that the separation becomes more relaxed. Incidentally, this phenomenon is observed in almost the same way in all other types of sand, even if the specific numerical values are different. So, porosity ε=33.0%
The Q value of Sagami River sand according to JISA1109 is 3.12%.
Although this is considerably higher than the case in Figure 5,
The same test and measurement results for this product are summarized in FIG. 6. In other words, in the case of this Sagami River sand, the fifth
In the same horizontal axis logarithmic graph as shown in the figure, the moisture content decreases almost linearly up to 3Q, but above 4Q, a clear inflection is observed at the position of 5 minutes of centrifugal force action, and in this case, around 3Q. Said
It is recognized that SWmax exists. In addition, each of the above-mentioned fine aggregates and other representative 5
Figure 7 shows the results of a similar centrifugal force separation test on seed fine aggregates whose initial moisture content was adjusted to around 1Q, with some fluctuations observed. However, it was confirmed that all fine aggregates remained almost unchanged regardless of the length of the separation treatment time, and from this result, it can be said that the test results according to JISA1109 are stable in terms of moisture content. In addition, in the above-mentioned test measurements, it is important to add attached water under reduced pressure conditions as mentioned above after measuring the absolute dry weight. If the pressure is reduced to -730 mmHg, the air adhering to the surface of the fine aggregate can be effectively removed, and if water is added and mixed in this state, the added water will damage the structure of the fine aggregate. The water is effectively permeated into the inside, and the attached moisture becomes stable and constant. On the other hand, if the mixture is simply mixed with water in the atmosphere, there is a high possibility that the adhering water will be unevenly distributed on the surface of the fine aggregate, and therefore it will be unstable and the measurement results will fluctuate. For example, the results of the same centrifugal separation treatment of the Oigawa E sand, which was kept in an absolutely dry state and mixed with water under the reduced pressure conditions in a vacuum mixer, and with water added in the air, are shown in Figure 8. However, even if the treatment time is the same, the measurement results will vary, and those mixed with water in the atmosphere have a low moisture content and have considerable variation. Those using reduced pressure conditions are almost stable with almost no fluctuation even in the repeated test results, and similar results were obtained with any of the above-mentioned Sagami river sand, water slag sand, or standard sand. In order to obtain accurate measurement results, it is essential to add water and mix under reduced pressure conditions to obtain a specified Q value for substances that have been confirmed and kept in an absolutely dry state for purposes such as weight measurements. However, for items that have been immersed in water for a fairly long period of time, such as 24 hours, equally accurate results can be obtained by testing and measuring them as they are (after that, the weight is measured in an absolutely dry state). It is necessary to maintain a constant water encounter history in at least the fine aggregate. Furthermore, to explain the results of examining various types of fine aggregates for centrifugal force separation as described above, 11 types of fine aggregates shown in Table 1 below each contained moisture equivalent to 3Q. These fine aggregates were subjected to centrifugal separation treatment using the same gravitational acceleration of 453 g as described above.The results are also shown in the lower part of Table 1 in relation to the elapsed treatment time.

【表】【table】

【表】 又このような結果を要約して図表としたのが第
9図であつて、縦軸における横軸0分の位置に採
られた値が夫々の細骨材における3Qに相当した
値であり、このものが夫々の処理時間で含水率を
何れも低下することとなるが、相模川川砂(×…
…×)および北米産砂以外は処理作用による含水
率低下が略整理とした平行関係にあり、何れも
120分の処理で表面乾燥飽水状態Qの2倍程度の
含水率となつており、第1表に示した粗粒率FM
の如何による影響や空隙率εによる影響を殆んど
受けないものと認められる。 然して上記したような結果を前記Qの倍率を以
て整理したのが第10図であつて、Q値との間に
直線的な相関関係が認められることは明かであ
り、これを更に処理時間30分、60分および120分
についてそれぞれ整理すると第11図a〜cのよ
うになる。即ち遠心力作用後の含水率と該細骨材
Q値との直線関係勾配は30分で2.5、60分で2.3、
120分で2.0であつて略整然とし、処理時間の長く
なる程小さくなるが何れも図表上整然としてい
る。然して前記相模川砂および北米産砂のように
前記図表上Q=2.5又は2.3或いは2.0の直線からそ
れなりにずれるものについて考察してみると、こ
のように基準ラインよりずれた値を採る所以は既
述したようなQ0(内部飽水率)によるものと認め
られ、その関係は少くとも30分以上の遠心分離処
理することによつて略同じである。従つて試験測
定のための必要時間を短縮し、しかも好ましい
SWmax或いはQ0値を得るためには前記のような
遠心力による分離処理の場合に30分とすることが
実用的である。 本発明によれば上記のようにして限界表面吸着
水率SWlin、最大表面吸着水率SWmaxの何れか
一方又は双方を求め得るものであり、又適宜に内
部飽水率Q0を考慮することができるもので、そ
れらの関係について表現してみると、最大表面吸
着水率SWmaxは細骨材の内部が飽水状態であつ
て、しかもその表面に吸着された水率であり、限
界表面吸着水率Swlimに対してそれぞれ実験条件
によつて定める実験係数Aを乗じた値であつて次
の式のように表わされる。 SWmax=A SWlim=A(Q−Q0) …… 然して一定条件下(例えば730mmHgで3Qの附
着水をもつた細骨材を453gの遠心力で30分間処
理)の実験値をSWgとすると、このSWgは、次
の式のようになる。 SWg=A SWlim+Q0 …… 又前記したような関係からして、今A=2.5で
Q0≒0とすると、SWlim=Qとなり、SWgは
2.5SWlim+0=2.5Q(SWmax=2.5Q)であり、
従つて、SWg/A=Q(SWg/2.5≒Q)であつて、この 場合のSWgはそのままSWmaxとして取扱つてよ
い。 又前記した第10,11図における相模川川砂
や北米産砂のように内部飽水率Q0の無視できな
い場合においてはSWg/A≠0であつて、SWg/2.5≠ Qであり、前記式よりSWlim=Q−Q0が導れ、
これを上記式に代入し整理すると次の式が誘
導されて内部飽水率が求められ、又SWlimなど
の表面吸着水関係も求め得る。 Q0=AQ−SWg/A−1 …… 以上説明したような本発明によれば、この種細
骨材に関して短時間内にその含水状態を測定解明
し得るもので、それによつて表面乾燥飽水状態の
みならず、内部飽水率Q0、固有表面吸着水率
SWlim、最大表面吸着水率SWmaxの如き従来技
術において解明されていない水率を適切に求めし
め、これを前記したようなモルタル又はコンクリ
ート混練物の調整に関して有効に利用せしめ合理
的且つ最適の配合条件を的確に得しめるものであ
るから工業的にその効果の大きい発明である。
[Table] Figure 9 is a diagram that summarizes these results, and the value taken at the 0 minute position on the horizontal axis on the vertical axis is the value corresponding to 3Q for each fine aggregate. The moisture content of this material decreases with each treatment time, but Sagami River sand (×...
…x) and North American sand, there is a roughly parallel relationship in which the moisture content decreases due to treatment effects, and in all cases
After 120 minutes of treatment, the moisture content was approximately twice that of the surface dry saturated state Q, and the coarse particle ratio FM shown in Table 1 was reached.
It is recognized that it is hardly affected by the porosity or the porosity ε. However, Figure 10 shows the above results organized by the multiplier of Q, and it is clear that there is a linear correlation between the Q value and the processing time of 30 minutes. , 60 minutes and 120 minutes are arranged as shown in Figures 11 a to c. In other words, the slope of the linear relationship between the moisture content after centrifugal force and the Q value of the fine aggregate is 2.5 at 30 minutes, 2.3 at 60 minutes,
It is 2.0 at 120 minutes, which is approximately regular, and decreases as the processing time increases, but both are regular on the graph. However, if we consider the aforementioned Sagami River sand and sand from North America, which deviate to some extent from the straight line of Q = 2.5, 2.3, or 2.0 on the chart, the reason why values deviate from the standard line in this way is already explained. It is recognized that this is due to the Q 0 (internal water saturation rate), and the relationship remains almost the same after centrifugation treatment for at least 30 minutes or more. Therefore, the time required for test measurements is shortened and is also preferable.
In order to obtain the SWmax or Q 0 value, it is practical to set the time to 30 minutes in the case of separation treatment using centrifugal force as described above. According to the present invention, either or both of the limit surface adsorption water rate SWlin and the maximum surface adsorption water rate SWmax can be determined as described above, and the internal water saturation rate Q 0 can be taken into consideration as appropriate. Expressing the relationship between them, the maximum surface adsorption water rate SWmax is the percentage of water adsorbed on the surface when the inside of the fine aggregate is saturated with water, and the limit surface adsorption water rate is It is a value obtained by multiplying the rate Swlim by an experimental coefficient A determined according to experimental conditions, and is expressed as the following equation. SWmax=A SWlim=A(Q-Q 0 )......If SWg is the experimental value under certain conditions (for example, treating fine aggregate with 3Q of attached water at 730 mmHg for 30 minutes with a centrifugal force of 453 g), then This SWg is expressed as the following formula. SWg=A SWlim+Q 0 ... Also, based on the relationship mentioned above, now A=2.5.
If Q 0 ≒ 0, then SWlim=Q, and SWg is
2.5SWlim+0=2.5Q (SWmax=2.5Q),
Therefore, SWg/A=Q (SWg/2.5≈Q), and SWg in this case can be treated as SWmax. Furthermore, in cases where the internal water saturation rate Q 0 cannot be ignored, such as the Sagami River sand and the North American sand in Figures 10 and 11 mentioned above, SWg/A≠0 and SWg/2.5≠Q, and the above formula From this, SWlim=Q−Q 0 can be derived,
By substituting this into the above equation and rearranging it, the following equation is derived and the internal water saturation rate can be determined, and surface adsorption water relationships such as SWlim can also be determined. Q 0 =AQ-SWg/A-1... According to the present invention as explained above, it is possible to measure and clarify the moisture content of this type of fine aggregate within a short time, thereby reducing surface dryness saturation. Not only the water state but also the internal water saturation rate Q 0 and the specific surface adsorption water rate
Appropriately determine water percentages that have not been elucidated in conventional technology, such as SWlim and maximum surface adsorption water rate SWmax, and use this effectively to adjust mortar or concrete mixes as described above to find rational and optimal mixing conditions. It is an invention that has great industrial effects because it can accurately obtain the following.

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

図面は本発明の技術的内容を示すものであつ
て、第1図は各種細骨材についてJIS規定による
表面乾燥飽水状態と空隙率の関係を示した図表、
第2図は本発明方法で用いる密閉容器の分解状態
を断面および平面図で示した説明図、第3図はそ
の結合状態の断面図、第4図はこれを用いた試験
装置全体の断面図、第5図は附着水量を種々に異
らしめた細骨材について本発明による測定をなし
た場合の遠心力作用時間と含水率の関係を要約し
て示した図表、第6図は第5図の場合とは異つた
細骨材について同様に測定をなした結果の図表、
第7図は各種細骨材について初期含水率を1Q前
後となるように調整したものについての同様の遠
心力分離試験結果を示したグラフ、第8図は大気
中で加水したものと減圧条件で加水したものにつ
いて同様の遠心力分離処理した結果の図表、第9
図は多様な細骨材について遠心力分離処理した結
果を要約して示すグラフ、第10図は第9図のも
のの初期含水率をQ値の倍率を以て整理した結果
を示す図表、第11図は更にこれを処理時間30
分、60分および120分について整理した結果の図
表である。 然してこれらの図面において、10は合成樹脂
管、11はアクリル板、12は金網、13は濾
紙、14は孔あき鉄板、15は接着テープ、16
は脱脂綿、20はケース、21は蓋、22は回転
板、23は回転軸、24は受器、25は軸を示す
ものである。
The drawings show the technical content of the present invention, and Figure 1 is a chart showing the relationship between the surface dry saturated state and the porosity according to JIS regulations for various fine aggregates.
Fig. 2 is an explanatory diagram showing the disassembled state of the sealed container used in the method of the present invention in cross section and plan view, Fig. 3 is a sectional view of the assembled state, and Fig. 4 is a sectional view of the entire test device using this. , Figure 5 is a diagram summarizing the relationship between centrifugal force action time and water content when measurements are made according to the present invention on fine aggregates with various amounts of adhering water; Diagrams and charts showing the results of similar measurements on fine aggregates different from those shown in the figure.
Figure 7 is a graph showing similar centrifugal force separation test results for various fine aggregates whose initial moisture content was adjusted to around 1Q, and Figure 8 is a graph showing the results of a similar centrifugal force separation test for various fine aggregates with the initial moisture content adjusted to around 1Q. Diagrams and charts of the results of similar centrifugal force separation treatment for water-added materials, No. 9
The figure is a graph summarizing the results of centrifugal separation treatment of various fine aggregates, Figure 10 is a graph showing the results of the initial moisture content of Figure 9 organized by Q value magnification, and Figure 11 is Furthermore, the processing time for this is 30
This is a chart showing the results organized for minutes, 60 minutes, and 120 minutes. In these drawings, 10 is a synthetic resin pipe, 11 is an acrylic plate, 12 is a wire mesh, 13 is a filter paper, 14 is a perforated iron plate, 15 is an adhesive tape, and 16
20 is absorbent cotton, 20 is a case, 21 is a lid, 22 is a rotating plate, 23 is a rotating shaft, 24 is a receiver, and 25 is a shaft.

Claims (1)

【特許請求の範囲】 1 湿潤化された細骨材を密閉容器内に収容せし
め、該密閉容器に所定時間の遠心力を作用せしめ
て細骨材附着水分の分離を図り、この遠心力作用
による分離処理後に細骨材に残留附着した水分を
測定し、前記細骨材の表面吸着水と内部飽水率を
求めることを特徴とする水硬性物質配合用細骨材
の含水率測定方法。 2 遠心力分離処理によつて除去された水分を吸
収材に吸着させて停止時においても細骨材に吸収
されないようにする特許請求の範囲第1項に記載
の細骨材の含水率測定方法。 3 密閉管状容器の中間部に濾材および適当な支
持部材をセツトし、該密閉管状容器の一側に湿潤
した細骨材を収容すると共に他側に水分吸収材を
収容したものの中間部を回転板に回動可能に軸支
し、該回転板の回動によつて前記密閉管状容器内
の細骨材に遠心力を作用させるようにした細骨材
の含水率測定装置。
[Scope of Claims] 1. Moisturized fine aggregate is placed in a closed container, centrifugal force is applied to the closed container for a predetermined period of time to separate water adhering to the fine aggregate, and moisture adhering to the fine aggregate is separated. 1. A method for measuring the moisture content of fine aggregate for blending hydraulic substances, characterized by measuring the moisture remaining attached to the fine aggregate after separation treatment, and determining the surface adsorbed water and internal water saturation rate of the fine aggregate. 2. A method for measuring the water content of fine aggregate according to claim 1, in which the water removed by centrifugal force separation is adsorbed onto an absorbent material so that it is not absorbed into the fine aggregate even during stoppage. . 3. A filter medium and a suitable support member are set in the middle part of a closed tubular container, and the middle part of the closed tubular container, which contains wet fine aggregate on one side and moisture absorbing material on the other side, is placed on a rotating plate. An apparatus for measuring moisture content of fine aggregate, which is rotatably supported on a shaft, and is configured to apply a centrifugal force to the fine aggregate in the sealed tubular container by rotation of the rotary plate.
JP521683A 1983-01-18 1983-01-18 Method and device for measuring moisture content in fine aggregate for compounding hydraulic material Granted JPS59131164A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP521683A JPS59131164A (en) 1983-01-18 1983-01-18 Method and device for measuring moisture content in fine aggregate for compounding hydraulic material
US06/882,034 US4715719A (en) 1983-01-18 1984-01-18 Method of preparing mortar or concrete
PCT/JP1984/000008 WO1984002872A1 (en) 1983-01-18 1984-01-18 Method of producing mortar or concrete
US06/788,227 US4686852A (en) 1983-01-18 1985-10-16 Method of preparing mortar or concrete

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP521683A JPS59131164A (en) 1983-01-18 1983-01-18 Method and device for measuring moisture content in fine aggregate for compounding hydraulic material

Publications (2)

Publication Number Publication Date
JPS59131164A JPS59131164A (en) 1984-07-27
JPH0521184B2 true JPH0521184B2 (en) 1993-03-23

Family

ID=11604988

Family Applications (1)

Application Number Title Priority Date Filing Date
JP521683A Granted JPS59131164A (en) 1983-01-18 1983-01-18 Method and device for measuring moisture content in fine aggregate for compounding hydraulic material

Country Status (1)

Country Link
JP (1) JPS59131164A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6333461U (en) * 1986-08-21 1988-03-03
JPH0752617Y2 (en) * 1987-07-18 1995-11-29 直俊 高田 Centrifugal force model loading device for soil structure
EP1902825B1 (en) * 2006-09-20 2011-11-09 ECON Maschinenbau und Steuerungstechnik GmbH Apparatus for dewatering and drying solid materials, especially plastics pelletized using an underwater granulator
JP4942777B2 (en) * 2009-01-28 2012-05-30 中国電力株式会社 Aggregate trace amount test method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5651317A (en) * 1979-10-01 1981-05-08 Ito Yasuro Method of preparing castable mixture such as cement

Also Published As

Publication number Publication date
JPS59131164A (en) 1984-07-27

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