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JPH0353356B2 - - Google Patents
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JPH0353356B2 - - Google Patents

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Publication number
JPH0353356B2
JPH0353356B2 JP58048525A JP4852583A JPH0353356B2 JP H0353356 B2 JPH0353356 B2 JP H0353356B2 JP 58048525 A JP58048525 A JP 58048525A JP 4852583 A JP4852583 A JP 4852583A JP H0353356 B2 JPH0353356 B2 JP H0353356B2
Authority
JP
Japan
Prior art keywords
coal
moisture content
increase
open
resin
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
JP58048525A
Other languages
Japanese (ja)
Other versions
JPS59174695A (en
Inventor
Shiro Hayashi
Kazuo Myata
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.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries Ltd
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 Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP4852583A priority Critical patent/JPS59174695A/en
Publication of JPS59174695A publication Critical patent/JPS59174695A/en
Publication of JPH0353356B2 publication Critical patent/JPH0353356B2/ja
Granted legal-status Critical Current

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Description

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

この発明は野積み石炭の含水率上昇抑制剤に関
し、さらに詳細には、野積み石炭の表面を疎水化
し、雨水の内部浸透を防止して、含水率の上昇を
抑制するための野積み石炭の含水率上昇抑制剤に
関するものである。 近年、石油シヨツクを契機に省エネルギー、省
資源が叫ばれ、同時にエネルギー源としての石炭
がその地位を回復するに及んで、その使用量も漸
次増大の傾向を辿つている。これに伴なつて石炭
貯蔵に関連する諸問題もクローズ・アツプされて
きた。例えば炭塵飛散、発熱防止、劣化防止等が
それで、その対策も種々考えられている。しかし
野積み石炭の雨水浸透防止については未だ本格的
な対策が講じられていない。 野積み石炭の雨水浸透による水分の上昇は、水
分蒸発のために余分のエネルギーを消費させ、経
済的に大きな損失を招くばかりでなく、原料炭の
場合はコークス製造工程において種々の悪影響を
及ぼす。従つて雨水による石炭の含水率の上昇を
1%抑制するだけでも大きなメリツトを生むこと
になる。 本発明は、このような状況下に、安価で優れた
野積み石炭の含水率上昇抑制剤を提供することを
目的とするものである。すなわち、本発明は、野
積み石炭の表面を疎水化し、雨水の内部浸透を防
止して、含水率の上昇を抑制するための野積み石
炭の含水率上昇抑制剤において、疎水性単量体の
重合体からなる樹脂の水中油型樹脂エマルシヨン
であつて、乳化剤を含まないか、または樹脂エマ
ルシヨン中の樹脂100重量部に対して乳化剤を1
重量部以下含有する水中油型樹脂エマルシヨンを
有効成分とすることを特徴とする野積み石炭の含
水率上昇抑制剤である。 野積み石炭の含水率上昇抑制剤は、野積み石炭
の少なくとも表面を疎水化し、雨水の内部浸透を
防止して、含水率の上昇を抑制する薬剤であり、
石炭の表面に疎水性の皮膜を形成することが要求
され、内部への浸透は必ずしも要求されない。一
方、粉塵飛散防止剤は風等により粉塵が飛散しな
いようにするために、相当の厚さにわたつて樹脂
を浸透させて、微粒子を団粒化ないし固化する薬
剤であるため、内部への浸透性が要求され、必ず
しも疎水化は要求されない。一般に樹脂エマルシ
ヨンは乳化安定性をもたせるために相当量の乳化
剤が使用されるが、特に粉塵飛散防止剤の場合に
は、内部への浸透性が要求されるので、多量の乳
化剤が使用される。発熱防止、劣化防止剤も空気
の侵入を遮断するために、相当の厚さにわたつて
固化する必要があり、同様に多量の乳化剤を用い
て内部まで浸透させる必要がある。ところが多量
の乳化剤を配合すると、親水性が付与されるた
め、水が浸透しやすくなり、含水率抑制剤として
は利用できない。 本発明では、野積み石炭の少なくとも表面を疎
水化すれば、雨水の内部への浸透を防止できると
いう現象を利用するものであり、このため樹脂の
内部への浸透性を犠牲にして、乳化剤の量を少な
くし、表面の疎水化を行う。このような含水率抑
制剤で処理した野積み石炭は、空気の侵入を防止
できないため、粉塵飛散防止、発熱防止、劣化防
止等の効果は劣るが、小量の薬剤使用量で効果的
に雨水の内部への浸透を防止し、含水率の上昇を
抑制することができる。 本発明の有効成分である水中油型樹脂エマルシ
ヨンは、疎水性単量体を乳化剤を用いずに、また
は用いる場合でも疎水性単量体重量の1%以下で
乳化重合して得ることができる。 本発明に用いられる疎水性単量体としては、酢
酸ビニル、アクリル酸エステル、メタクリル酸エ
ステル、スチレン、エチレン、ブタジエン、塩化
ビニル、塩化ビニリデンなどが挙げられ、これら
の1種または2種以上の混合物が乳化重合に供さ
れる。また、これらの疎水性単量体はカチオン性
単量体と共重合してもよく、その場合カチオン性
単量体は、全単量体の10wt%以下程度とすると
よい。カチオン性単量体としては、メタクリロイ
ルオキシエチルトリメチルアンモニウムクロライ
ド、メタクリルアミドプロピルトリメチルアンモ
ニウムクロライド、ビニルピリジン等を用いるこ
とができる。 乳化剤としては、カチオン性、アニオン性また
はノニオン性のいずれの界面活性剤を用いてもよ
い。 カチオン性界面活性剤としては、炭素数12以上
の脂肪族炭化水素基を有する第1級アミン塩、第
2級アミン塩、第3級アミン塩、および第4級ア
ンモニウム塩が用いられ、この中でも、第4級ア
ンモニウム塩型が好ましい。この第4級アンモニ
ウム塩型のカチオン性界面活性剤としては、例え
ば、ラウリルトリメチルアンモニウムクロライ
ド、セチルトリメチルアンモニウムクロライド、
ステアリルトリメチルアンモニウムクロライドな
どが挙げられる。 アニオン性界面活性剤としては、アルキルスル
ホン酸ナトリウム、アルキルベンゼンスルホン酸
ナトリウム、ポリオキシエチレンアルキルエーテ
ル硫酸エステルのナトリウム塩、ポリオキシエチ
レンフエニルエーテル硫酸エステルのナトリウム
塩、高級アルコール硫酸エステルのナトリウム
塩、ロート油等が挙げられる。 ノニオン性界面活性剤としては、ポリオキシエ
チレンアルキルフエニルエーテル、ポリオキシエ
チレンアルキルエーテル、ポリオキシエチレンポ
リオキシプロピレンエーテルなどが、用いられる
が、HLBが16以上のものが好ましい。 乳化重合は、疎水性単量体を必要に応じ乳化剤
と共に水中で撹拌分散し、窒素ガスを吹込みなが
ら加温し、過酸化ベンゾイル、過硫酸塩、過酸化
水素などの触媒や、これらの酸化剤とチオ硫酸ナ
トリウム、亜硫酸水素ナトリウムなどの還元剤と
を組み合せたレドツクス触媒を用いて行う。ま
た、触媒のほかに硫酸銅のような重合促進剤を用
いると、生成するエマルシヨンの樹脂粒子が小さ
くなり乳化安定性がよくなるので好ましい。 乳化剤は用いないのが好ましいが、用いるとき
は、疎水性単量体重量の1%以下としなければな
らない。また、一般に乳化重合時または重合後の
乳化安定性を高めるために、ポリビニルアルコー
ルやカルボキシメチルセルロースなどの保護コロ
イドを用いることがあるが、本発明においては乳
化剤や保護コロイドを用いない方が好ましい。な
ぜならば、乳化剤や保護コロイドを多量に含む水
中油型エマルシヨンを石炭に散布すると、これら
の物質がエマルシヨン粒子間に介在することによ
り、粒子の合一が妨げられ、樹脂皮膜の生成に長
時間を要し、また生成した皮膜の透水性を増大さ
せる原因となるからである。 本発明の野積み石炭の含水率上昇抑制剤は、通
常、樹脂分5〜10%の濃度で用い、野積み石炭に
対しては、石炭山表面1m2当り樹脂分として25〜
200g、好ましくは50〜100g散布する。その際、
散布機を用いて、石炭山の全表面に対して均一に
散布するとよい。なお、薬剤の散布は一回だけで
もよいが、複数回行つてもよい。また次のように
用いてもよい。 石炭山の形成時に、その表層部となる移送中
の石炭にベルトコンベア上で散布する。 石炭山の形成時に、移送中の石炭のすべてに
ベルトコンベア上で散布する。 またはに記載の散布を行い石炭山を形成
したのち、さらにその表層部に散布する。 本発明の野積み石炭の含水率上昇抑制剤を野積
み石炭に散布すると、樹脂皮膜の形成が促進さ
れ、樹脂皮膜と石炭とが強く結合して石炭山の表
面を強固にし、また、石炭山表面の石炭を疎水化
する。したがつて、雨水の内部浸透を防止するこ
とができ、石炭の含水率上昇を抑制することがで
きる。なお、皮膜が強固なため、激しい降雨によ
つて石炭山が崩壊することの防止効果も期待でき
る。 次に実施例を挙げて、本発明を詳しく説明す
る。 実施例 4メツシユのふるいを通過したグーニエラ炭3
Kgを表層水と透過水とを分取できる円形容器(直
径30cm)上に円錐状に山積みし、これに第1表に
示す各種樹脂エマルシヨンを、樹脂分濃度を5%
に調整したのち均一に散布し、3日間室内で風乾
した。次にこれを降雨強度10mm/hrの人工降雨下
に20時間曝した後、表層水量、透過水量及び山積
み石炭の重量変化(降雨前後の重量差)を測定
し、全水分および浸透率を求めた。結果を第2表
に示す。降雨後の全水分は、降雨前の全水分と重
量変化から次式により算出した。 降雨後全水分(%)=降雨前石炭重量(g)×降雨前全
水分(%)×10-2+重量変化(Δg)/降雨前石炭重量
(g)+重量変化(Δg)×100 また、浸透率は次式により算出した。 浸透率(%)=透過水量(g)+重量変化
(Δg)/表層水量(g)+透過水量(g)+重量変化
(Δg)×100
The present invention relates to an agent for suppressing an increase in moisture content of open piled coal, and more particularly, to an agent for suppressing an increase in moisture content of open piled coal by making the surface of the open piled coal hydrophobic and preventing rainwater from penetrating into the inside of the piled coal. This invention relates to a moisture content increase inhibitor. In recent years, energy and resource conservation have been called for in the wake of oil shocks, and at the same time, as coal has regained its position as an energy source, its usage has also been on the rise. Along with this, various issues related to coal storage have also been brought into focus. For example, various countermeasures are being considered, such as preventing coal dust from scattering, preventing heat generation, and preventing deterioration. However, no serious measures have yet been taken to prevent rainwater from seeping into open coal piles. The increase in water content due to the infiltration of rainwater in open piled coal not only consumes extra energy for water evaporation, resulting in large economic losses, but also has various negative effects on the coke manufacturing process in the case of coking coal. Therefore, even if the increase in moisture content of coal due to rainwater is suppressed by 1%, it will bring about great benefits. Under such circumstances, it is an object of the present invention to provide an inexpensive and excellent inhibitor of increase in moisture content of open coal. That is, the present invention provides a moisture content increase inhibitor for open piled coal for hydrophobicizing the surface of the piled coal to prevent internal penetration of rainwater and suppressing the increase in moisture content. An oil-in-water resin emulsion of a resin consisting of a polymer, which does not contain an emulsifier or contains 1 emulsifier per 100 parts by weight of the resin in the resin emulsion.
This is an agent for suppressing an increase in the water content of piled coal, characterized in that the active ingredient is an oil-in-water resin emulsion containing not more than parts by weight. The moisture content increase inhibitor of open piled coal is an agent that hydrophobicizes at least the surface of open piled coal, prevents rainwater from penetrating into the inside, and suppresses an increase in moisture content.
It is required to form a hydrophobic film on the surface of the coal, and penetration into the interior is not necessarily required. On the other hand, dust scattering prevention agents are agents that penetrate resin over a considerable thickness and aggregate or solidify fine particles in order to prevent dust from scattering due to wind, etc. hydrophobicity is not necessarily required. Generally, resin emulsions use a considerable amount of emulsifier in order to provide emulsion stability, but especially in the case of dust scattering prevention agents, a large amount of emulsifier is used because internal penetration is required. The anti-heat generation and anti-deterioration agent also needs to be solidified to a considerable thickness in order to block air from entering, and similarly it is necessary to use a large amount of emulsifier to penetrate into the inside. However, when a large amount of emulsifier is blended, hydrophilicity is imparted to the composition, making it easy for water to penetrate, making it impossible to use it as a moisture content inhibitor. The present invention utilizes the phenomenon that by making at least the surface of piled coal hydrophobic, it is possible to prevent rainwater from penetrating into the interior.For this reason, the emulsifier is reduced at the cost of sacrificing the penetrability of the resin into the interior. Reduce the amount and make the surface hydrophobic. Open piled coal treated with such moisture content inhibitors cannot prevent air from entering, so it is less effective in preventing dust scattering, heat generation, deterioration, etc., but with a small amount of the agent used, rainwater can be effectively removed. It is possible to prevent water from penetrating into the interior and suppress an increase in moisture content. The oil-in-water resin emulsion, which is the active ingredient of the present invention, can be obtained by emulsion polymerization of hydrophobic monomers without using an emulsifier, or even if an emulsifier is used, the amount is 1% or less of the weight of the hydrophobic monomer. Examples of the hydrophobic monomer used in the present invention include vinyl acetate, acrylic ester, methacrylic ester, styrene, ethylene, butadiene, vinyl chloride, vinylidene chloride, etc. One type or a mixture of two or more of these monomers can be used. is subjected to emulsion polymerization. Further, these hydrophobic monomers may be copolymerized with a cationic monomer, and in this case, the cationic monomer is preferably about 10 wt% or less of the total monomers. As the cationic monomer, methacryloyloxyethyltrimethylammonium chloride, methacrylamide propyltrimethylammonium chloride, vinylpyridine, etc. can be used. As the emulsifier, any cationic, anionic or nonionic surfactant may be used. As the cationic surfactant, primary amine salts, secondary amine salts, tertiary amine salts, and quaternary ammonium salts having an aliphatic hydrocarbon group having 12 or more carbon atoms are used, and among these, , quaternary ammonium salt type is preferred. Examples of the quaternary ammonium salt type cationic surfactant include lauryltrimethylammonium chloride, cetyltrimethylammonium chloride,
Examples include stearyltrimethylammonium chloride. Examples of anionic surfactants include sodium alkyl sulfonate, sodium alkylbenzene sulfonate, sodium salt of polyoxyethylene alkyl ether sulfate, sodium salt of polyoxyethylene phenyl ether sulfate, sodium salt of higher alcohol sulfate, and Examples include oil. As the nonionic surfactant, polyoxyethylene alkyl phenyl ether, polyoxyethylene alkyl ether, polyoxyethylene polyoxypropylene ether, etc. are used, but those having an HLB of 16 or more are preferred. In emulsion polymerization, hydrophobic monomers are stirred and dispersed in water together with an emulsifier if necessary, heated while blowing nitrogen gas, and a catalyst such as benzoyl peroxide, persulfate, hydrogen peroxide, etc. This is carried out using a redox catalyst that combines a chemical agent and a reducing agent such as sodium thiosulfate or sodium bisulfite. Further, it is preferable to use a polymerization accelerator such as copper sulfate in addition to the catalyst because the resin particles of the resulting emulsion become smaller and the emulsion stability becomes better. Emulsifiers are preferably not used, but if used, they should be used in an amount of 1% or less of the weight of the hydrophobic monomer. Further, in order to generally improve emulsion stability during or after emulsion polymerization, a protective colloid such as polyvinyl alcohol or carboxymethyl cellulose may be used, but in the present invention it is preferable not to use an emulsifier or a protective colloid. This is because when an oil-in-water emulsion containing large amounts of emulsifiers and protective colloids is sprayed onto coal, these substances interpose between the emulsion particles, preventing the particles from coalescing and making it take a long time to form a resin film. This is because it is necessary and causes an increase in the water permeability of the formed film. The moisture content increase inhibitor for open piled coal of the present invention is usually used at a concentration of 5 to 10% resin content, and for open pile coal, the resin content is 25 to 25% per square meter of coal pile surface.
Spread 200g, preferably 50-100g. that time,
It is best to use a spreader to spread it evenly over the entire surface of the coal pile. Note that the chemical may be sprayed only once, or may be sprayed multiple times. It may also be used as follows. When a coal pile is formed, it is spread on the conveyor belt to the coal that is being transported and forms the surface layer of the pile. When the coal pile is formed, all of the coal being transported is spread on the conveyor belt. After forming a coal pile by performing the spraying described in or, further spraying is performed on the surface layer of the coal pile. When the moisture content increase inhibitor for open piled coal of the present invention is sprayed on open piled coal, the formation of a resin film is promoted, and the resin film and coal are strongly bonded to strengthen the surface of the coal pile. Hydrophobizes the coal on the surface. Therefore, internal infiltration of rainwater can be prevented, and an increase in the moisture content of coal can be suppressed. Furthermore, since the film is strong, it can also be expected to prevent coal piles from collapsing due to heavy rainfall. Next, the present invention will be explained in detail with reference to Examples. Example 4 Goonyera charcoal 3 passed through mesh sieve
Kg is piled up in a conical shape on a circular container (diameter 30 cm) that can separate surface water and permeated water, and various resin emulsions shown in Table 1 are added to this at a resin concentration of 5%.
After adjusting the amount, it was evenly spread and air-dried indoors for 3 days. Next, after exposing this to artificial rain with a rainfall intensity of 10 mm/hr for 20 hours, the amount of surface water, amount of permeated water, and change in weight of the piled coal (difference in weight before and after rain) were measured to determine total moisture and permeation rate. . The results are shown in Table 2. The total moisture after rain was calculated from the total moisture before rain and weight change using the following formula. Total moisture after rain (%) = Coal weight before rain (g) x Total moisture before rain (%) x 10 -2 + Weight change (Δg) / Coal weight before rain (g) + Weight change (Δg) x 100 The penetration rate was calculated using the following formula. Permeation rate (%) = Permeated water amount (g) + Weight change (Δg) / Surface water amount (g) + Permeated water amount (g) + Weight change (Δg) × 100

【表】【table】

【表】【table】

【表】 第2表から、乳化剤を含まないか、樹脂分に対
して1%以下の乳化剤を含む樹脂エマルシヨン
は、乳化剤を多く含むものに比べ石炭の含水率上
昇抑制効果が優れていることがわかる。 実施例 2 第3表に示す樹脂エマルシヨンを用いて、実施
例1と同様に試験を行い、全水分および浸透率を
求めた。結果は第4表に示す。
[Table] Table 2 shows that resin emulsions that do not contain an emulsifier or that contain less than 1% emulsifier based on the resin content are more effective in suppressing increases in the moisture content of coal than those that contain a large amount of emulsifier. Recognize. Example 2 Using the resin emulsions shown in Table 3, tests were conducted in the same manner as in Example 1 to determine the total water content and permeability. The results are shown in Table 4.

【表】【table】

【表】 第4表から、樹脂エマルシヨンは保護コロイド
を含まない方が効果がよいことがわかる。
[Table] From Table 4, it can be seen that the resin emulsion is more effective when it does not contain a protective colloid.

Claims (1)

【特許請求の範囲】 1 野積み石炭の表面を疎水化し、雨水の内部浸
透を防止して、含水率の上昇を抑制するための野
積み石炭の含水率上昇抑制剤において、疎水性単
量体の重合体からなる樹脂の水中油型樹脂エマル
シヨンであつて、乳化剤を含まないか、または樹
脂エマルシヨン中の樹脂100重量部に対して乳化
剤を1重量部以下含有する水中油型樹脂エマルシ
ヨンを有効成分とすることを特徴とする野積み石
炭の含水率上昇抑制剤。 2 樹脂エマルシヨンは、保護コロイドを含有し
ないものである特許請求の範囲第1項記載の野積
み石炭の含水率上昇抑制剤。
[Claims] 1. An agent for suppressing the increase in moisture content of open coal, which hydrophobicizes the surface of open coal, prevents rainwater from penetrating inside, and suppresses an increase in moisture content, which comprises a hydrophobic monomer. The active ingredient is an oil-in-water resin emulsion of a resin made of a polymer of A moisture content increase inhibitor for open piled coal, characterized by: 2. The inhibitor for moisture content increase in open coal as claimed in claim 1, wherein the resin emulsion does not contain a protective colloid.
JP4852583A 1983-03-23 1983-03-23 Inhibitor against rise in content of coal in open-air storage Granted JPS59174695A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4852583A JPS59174695A (en) 1983-03-23 1983-03-23 Inhibitor against rise in content of coal in open-air storage

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4852583A JPS59174695A (en) 1983-03-23 1983-03-23 Inhibitor against rise in content of coal in open-air storage

Publications (2)

Publication Number Publication Date
JPS59174695A JPS59174695A (en) 1984-10-03
JPH0353356B2 true JPH0353356B2 (en) 1991-08-14

Family

ID=12805775

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4852583A Granted JPS59174695A (en) 1983-03-23 1983-03-23 Inhibitor against rise in content of coal in open-air storage

Country Status (1)

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JP (1) JPS59174695A (en)

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US5536429A (en) * 1992-04-29 1996-07-16 Benetech, Inc. Method for treating coke and coal and products produced thereby
US5310494A (en) * 1992-04-29 1994-05-10 Natec Resources, Inc. Method for controlling dusting of coke and coal
US9267063B2 (en) 2012-11-19 2016-02-23 Benetech, Inc. Dust suppression formulas using plasticized cellulose ethers

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JPS5431477B2 (en) * 1972-07-21 1979-10-06
CS187697B1 (en) * 1976-07-06 1979-02-28 Milan Chrtek Method of and apparatus for cooling spinning units of open-end spinning machines
JPS5674191A (en) * 1979-11-22 1981-06-19 Mitsui Eng & Shipbuild Co Ltd Granulation of coal for coal slurry transportation

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JPS59174695A (en) 1984-10-03

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