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JPH0380801B2 - - Google Patents
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JPH0380801B2 - - Google Patents

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Publication number
JPH0380801B2
JPH0380801B2 JP60136391A JP13639185A JPH0380801B2 JP H0380801 B2 JPH0380801 B2 JP H0380801B2 JP 60136391 A JP60136391 A JP 60136391A JP 13639185 A JP13639185 A JP 13639185A JP H0380801 B2 JPH0380801 B2 JP H0380801B2
Authority
JP
Japan
Prior art keywords
serum
rubber
natural rubber
spray
rubber latex
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
JP60136391A
Other languages
Japanese (ja)
Other versions
JPS61293201A (en
Inventor
Yoshio Tajima
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.)
Yokohama Rubber Co Ltd
Original Assignee
Yokohama Rubber Co 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 Yokohama Rubber Co Ltd filed Critical Yokohama Rubber Co Ltd
Priority to JP60136391A priority Critical patent/JPS61293201A/en
Priority to GB8614585A priority patent/GB2178045B/en
Priority to IDP287486A priority patent/ID805B/en
Priority to CN86104275A priority patent/CN1011860B/en
Publication of JPS61293201A publication Critical patent/JPS61293201A/en
Priority to MYPI87000097A priority patent/MY102130A/en
Publication of JPH0380801B2 publication Critical patent/JPH0380801B2/ja
Granted legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • C08J3/122Pulverisation by spraying
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23KFODDER
    • A23K10/00Animal feeding-stuffs
    • A23K10/30Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms
    • A23K10/37Animal feeding-stuffs from material of plant origin, e.g. roots, seeds or hay; from material of fungal origin, e.g. mushrooms from waste material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86Catalytic processes
    • B01D53/8671Removing components of defined structure not provided for in B01D53/8603 - B01D53/8668
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/85Chromium, molybdenum or tungsten
    • B01J23/86Chromium
    • B01J23/868Chromium copper and chromium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/84Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/889Manganese, technetium or rhenium
    • B01J23/8892Manganese
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C1/00Treatment of rubber latex
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25DREFRIGERATORS; COLD ROOMS; ICE-BOXES; COOLING OR FREEZING APPARATUS NOT OTHERWISE PROVIDED FOR
    • F25D23/00General constructional features
    • F25D23/02Doors; Covers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2389/00Characterised by the use of proteins; Derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P60/00Technologies relating to agriculture, livestock or agroalimentary industries
    • Y02P60/80Food processing, e.g. use of renewable energies or variable speed drives in handling, conveying or stacking
    • Y02P60/87Re-use of by-products of food processing for fodder production

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Physiology (AREA)
  • Mechanical Engineering (AREA)
  • Zoology (AREA)
  • Animal Husbandry (AREA)
  • Mycology (AREA)
  • Molecular Biology (AREA)
  • Botany (AREA)
  • Combustion & Propulsion (AREA)
  • Physics & Mathematics (AREA)
  • Food Science & Technology (AREA)
  • Thermal Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Biomedical Technology (AREA)
  • Analytical Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Description

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

<技術分野> 本発明は、天然ゴム製造時に副生する漿液から
得られる有用な粉末状の非ゴム成分に関する。 <従来技術> ゴム含有植物は極めて多種類の植物が発見され
ているが、工業用原料として今日栽培されている
のはゴム樹と呼ばれるヘベア・ブラジリエンシス
である。ゴム樹から得られる白色の乳状液(ラテ
ツクスという)の組成は、約35wt%のゴム分
(ゴム炭化水素)と、約5wt%のタンパク質、脂
肪酸、糖分等よりなる非ゴム分と、残りは水分で
ある。これらの成分が水を分散媒としてゴム炭化
水素を分散相とした疎水性コロイドゾルを形成し
ている。 一般にRSS(リブド スモークド シート)や
ブラウン クレープ等の天然ゴムを製造するに
は、ラテツクスを水で希釈しごみを除去した後、
凝固剤として蟻酸、酢酸、硫酸等を添加してゴム
分を凝固し、漿液(Serum)をしぼり出し除去
し、脱水乾燥し、微生物によるゴムの変質防止の
ために燻煙等の工程を行う。 天然ゴム製造工程で、凝固したゴム分を取り除
いた残りの液が、漿液(Serum)と呼ばれる水溶
液で、従来、そのまゝ廃棄される場合が多く、そ
の中に含まれる蛋白質、糖質等の非ゴム分の腐敗
により、環境汚染の問題があつた。漿液を浄化処
理槽で処理する方法もあるが、莫大な費用がかか
る割には、腐敗臭が激しく、公害問題ともなり、
効果があがつていない。 またこの漿液を、工業的有用物質として利用で
きれば、ゴム工業の効率もあがり、省資源に有効
であるが、未だそのような物質は製造されていな
い。 <発明の目的> 本発明の目的は、天然ゴムラテツクス漿液から
得られる工業的有用物質を提供するものである。 <発明の構成> 第1の発明は、天然ゴムラテツクス中のゴム成
分を凝固除去した残りの漿液を150〜250℃の高温
雰囲気中へスプレードライし、水分を蒸発させて
平均粒径10〜100μの粉末状としてなることを特
徴とする天然ゴムラテツクス漿液から得られる粉
末状非ゴム成分である。 前記スプレードライは、試料入口乾燥温度150
〜250℃、試料出口温度50〜130℃のスプレードラ
イ容器内へのスプレードライであるのがよい。 前記スプレードライ工程がデイスク回転体を用
いて行われデイスク回転体の回転数が10000〜
30000r.p.mであることが好ましい。 あるいは、前記スプレードライ工程がノズルを
用いて行われノズルによる漿液の滴下がノズル吹
出圧力0.5〜2.0Kg/cm2であることが良い。 以下に本発明をさらに詳細に説明する。 本発明の天然ゴムラテツクス漿液から得られる
粉末状非ゴム成分は、ほぼ球状の粉末であり、平
均粒径は10〜100μである。成分組成は原料であ
る天然ゴムラテツクスの成分によつて異なり厳密
に限定することはできないが、α−グロブリン、
ヘベインなどの蛋白質、脂肪酸、アミノ酸、糖
分、水、K、Mg、Cu、Fe、Na、Ca、P、等の
灰分(無機成分)、その他の微量成分である。1
例として後に述べる実施例5で得られた粉末状非
ゴム成分に含有されている蛋白質、アミノ酸の日
本食品分析センターによる分析結果を第3表に示
す。 本発明の天然ゴムラテツクス漿液から得られる
粉末状非ゴム成分は原料の天然ゴムラテツクスか
ら凝固剤として蟻酸、酢酸、硫酸等を用いてゴム
分を凝固し取り除いた、残りの漿液(serum)を
150〜250℃の高温雰囲気中へスプレードライし、
水分を蒸発させて製造する。 天然ゴムラテツクスの成分は1例をあげると第
1表に示す組成である。
<Technical Field> The present invention relates to a useful powdered non-rubber component obtained from serum produced as a by-product during the production of natural rubber. <Prior Art> A wide variety of rubber-containing plants have been discovered, but the one currently cultivated as an industrial raw material is Hevea brasiliensis, which is called the rubber tree. The white emulsion (called latex) obtained from rubber trees has a composition of about 35wt% rubber content (rubber hydrocarbons), about 5wt% non-rubber content consisting of proteins, fatty acids, sugars, etc., and the rest is water. It is. These components form a hydrophobic colloidal sol with water as a dispersion medium and rubber hydrocarbon as a dispersed phase. Generally, in order to produce natural rubber such as RSS (ribbed smoked sheet) and brown crepe, latex is diluted with water, dirt is removed, and then
Formic acid, acetic acid, sulfuric acid, etc. are added as a coagulant to coagulate the rubber, the serum is squeezed out and removed, dehydrated and dried, and processes such as smoking are performed to prevent the rubber from deteriorating due to microorganisms. In the natural rubber manufacturing process, the remaining liquid after removing the coagulated rubber is an aqueous solution called serum, which is traditionally discarded as is, and the proteins, carbohydrates, etc. contained in it are often discarded. There was a problem of environmental pollution due to the decomposition of non-rubber components. There is a method of treating the serum in a septic tank, but it is very expensive, emits a strong putrid odor, and poses a pollution problem.
The effect is not increasing. Furthermore, if this serum could be used as an industrially useful substance, it would improve the efficiency of the rubber industry and be effective in saving resources, but such a substance has not yet been produced. <Object of the invention> The object of the invention is to provide an industrially useful substance obtained from natural rubber latex serum. <Structure of the Invention> The first invention is to spray-dry the remaining serum after coagulating and removing the rubber components in natural rubber latex in a high temperature atmosphere of 150 to 250°C, evaporate the moisture, and form particles with an average particle size of 10 to 100μ. This is a powdery non-rubber component obtained from natural rubber latex serum, which is characterized by being in the form of a powder. The spray drying has a sample inlet drying temperature of 150
It is preferable to spray dry the sample into a spray drying container at ~250°C and a sample outlet temperature of 50~130°C. The spray drying process is performed using a disk rotating body, and the rotation speed of the disk rotating body is 10,000 to 10,000.
Preferably it is 30000r.pm. Alternatively, it is preferable that the spray drying step is performed using a nozzle and the serum is dripped by the nozzle at a nozzle blowing pressure of 0.5 to 2.0 Kg/cm 2 . The present invention will be explained in more detail below. The powdered non-rubber component obtained from the natural rubber latex serum of the present invention is a substantially spherical powder with an average particle size of 10 to 100 microns. The composition of ingredients varies depending on the ingredients of the raw material natural rubber latex and cannot be strictly limited, but it includes α-globulin,
These include proteins such as hevein, fatty acids, amino acids, sugar, water, ash (inorganic components) such as K, Mg, Cu, Fe, Na, Ca, P, and other trace components. 1
As an example, Table 3 shows the analysis results of the proteins and amino acids contained in the powdered non-rubber component obtained in Example 5, which will be described later, by the Japan Food Research Center. The powdered non-rubber component obtained from the natural rubber latex serum of the present invention is obtained by coagulating and removing the rubber content from the natural rubber latex as a raw material using formic acid, acetic acid, sulfuric acid, etc. as a coagulant.
Spray dry in a high temperature atmosphere of 150 to 250℃,
Manufactured by evaporating water. One example of the components of natural rubber latex is shown in Table 1.

【表】 この天然ゴムラテツクスからゴム炭化水素を除
いたものを漿液といい、一般に工業的には漿液中
には、ごく少量のゴム分が含まれているのが普通
である。 漿液の成分は天然ゴムラテツクスの成分によつ
て異なり、種々のものを原料とすることができる
が、漿液中には約0.5wt%のゴム分と非ゴム分約
2.0wt%が含まれる。これを遠心分離等にかけ、
ゴム分を除去して用いてもよい。 非ゴム分(固型分)濃度は、2〜50wt%のも
のを用いることができるが、生産効率、製造コス
トおよび工程管理の点で固型分15〜35wt%の漿
液を原料とすることが好ましい。通常天然ゴム製
造工程で得られる漿液の固型分は、約3〜5wt%
であるので、エバポレーター、遠心分離、濾過等
の方法で固型分濃度を25〜35wt%程度に濃縮す
る前処理をすることが良い。 上記漿液を150〜250℃の高温雰囲気のスプレー
ドライ容器内へ微小滴状にて供給し、瞬時に水分
を蒸発させて粉末状とする。このためクローズド
システムのスプレードライ方式を用いる。クロー
ズドシステムのスプレードライ方式は、液体試料
を微粒化し、微粒化された液滴を熱風と瞬間的に
接触させて、水分を蒸発させ乾燥して粉末化する
ものであり、加圧ノズルや二流体ノズルで微粒化
するノズル式と、高速回転円板で微粒化するデイ
スク式がある。いずれを用いてもよいがデイスク
式が効率が良く、好ましい。デイスクの回転数は
10000〜30000rpm、ノズルの圧力は0.5〜2.0Kg/
cm2が良い。回転数や圧力がこの範囲外になると得
られる粉末の大きさが10〜100μの範囲外となり、
10μ未満の粉末であると吸湿して再凝固しやすく
なつたり、スプレードライヤーの内壁に付着した
り凝集したりして回収率が悪くなり、得られる粉
末がダンゴ状のものとなり微粒化しない。100μ
を超えると非ゴム成分を工業的に利用する際に水
や溶剤に溶解しにくく、またカサが大きくなり運
搬に不便となる。 スプレードライ容器内の乾燥温度は150〜250℃
に保ち、特に試料入口乾燥温度を150〜250℃と
し、試料出口温度を50〜130℃とすることが好ま
しい。 試料乾燥温度がこの温度範囲より高くなると、
得られる非ゴム成分が熱により変質してしまう。
非ゴム成分は蛋白質、糖分、樹脂等でいづれも熱
的影響を受け易い。実際の試料温度は入口温度か
ら約100℃低い温度なので、その点からも乾燥温
度は余り高くはできない。又逆にこの温度範囲よ
り低い温度であると充分に乾燥ができず、粉末状
とならずに凝集してダンゴ状となる。 本発明の天然ゴムラテツクス漿液から得られる
粉末状非ゴム成分は、合成ゴム改質剤、加硫促進
剤、ゴム補強性充填剤のコーテイング剤、飼料、
医薬品等に利用することができ工業的に有用であ
る。有用性の詳細の一例を、本出願人の特願昭60
−136390号(特公平02−55372号)、特願昭60−
136392号(特公平03−51737号)に述べる。 <実施例> 第2表に示す組成の原料ラテツクスを用い、第
2表に示す製法で、粉末状非ゴム成分を作製し
た。実施例5で得られた粉末状非ゴム成分に含有
されている蛋白質とアミノ酸の分析結果を第3表
に示した。 スプレー方式に使用した装置は、ノズルタイ
プ・スプレードライヤー:ヤマト科学(株)製L−5
(DL−41)型、デイスクタイプ・スプレードライ
ヤー:大川原化工機(株)製L−12型である。 非ゴム成分(固型分)は、ケツト(Kett)社
の自動水分測定器により測定した。粘度はB型粘
度計で測定した。 べつに、比較例として実施例4、5で用いたと
同様の原料ラテツクスを用い、第2表に示したデ
イスク回転数と試料乾燥温度により処理したもの
を作製した。 得られた実施例と比較例の試料の平均粒子径、
粒子の形状、水分率、粒子の色、粒子の状態を測
定し、第2表に示した。 水分率はケツト(Kett)社の自動水分測定器
により測定した。
[Table] This natural rubber latex from which rubber hydrocarbons have been removed is called serum, and in general, industrially, serum usually contains a very small amount of rubber. The components of the serum vary depending on the components of the natural rubber latex, and various materials can be used as raw materials, but the serum contains about 0.5wt% rubber and about 0.5wt% non-rubber
Contains 2.0wt%. This is subjected to centrifugation, etc.
It may also be used after removing the rubber component. A non-rubber content (solid content) concentration of 2 to 50 wt% can be used, but from the viewpoint of production efficiency, manufacturing cost, and process control, it is preferable to use serum with a solid content of 15 to 35 wt% as a raw material. preferable. Normally, the solid content of the serum obtained in the natural rubber manufacturing process is approximately 3 to 5 wt%.
Therefore, it is preferable to carry out pretreatment to concentrate the solid content to about 25 to 35 wt% using a method such as an evaporator, centrifugation, or filtration. The serum is supplied in the form of minute droplets into a spray-drying container in a high-temperature atmosphere of 150 to 250°C, and water is instantly evaporated to form a powder. For this reason, a closed system spray drying method is used. The closed system spray drying method atomizes a liquid sample and instantly contacts the atomized droplets with hot air to evaporate water and dry them into powder. There are two types: the nozzle type, which uses a nozzle to atomize the particles, and the disk type, which uses a high-speed rotating disk to atomize the particles. Although any method may be used, the disk type is preferable because it is efficient. The rotation speed of the disk is
10000~30000rpm, nozzle pressure 0.5~2.0Kg/
cm2 is good. If the rotation speed or pressure is outside this range, the size of the powder obtained will be outside the range of 10 to 100μ,
If the powder is less than 10μ, it absorbs moisture and is likely to re-solidify, or it may adhere to or aggregate on the inner wall of the spray dryer, resulting in a poor recovery rate, and the resulting powder will be lump-like and not atomized. 100μ
If the non-rubber component is used industrially, it will be difficult to dissolve in water or solvents, and the bulk will become large, making transportation inconvenient. The drying temperature in the spray dry container is 150-250℃
In particular, it is preferable to keep the sample inlet drying temperature at 150 to 250°C and the sample outlet temperature to 50 to 130°C. If the sample drying temperature is higher than this temperature range,
The resulting non-rubber component changes in quality due to heat.
Non-rubber components include proteins, sugars, resins, etc., all of which are easily affected by heat. The actual sample temperature is about 100°C lower than the inlet temperature, so from that point of view the drying temperature cannot be set too high. On the other hand, if the temperature is lower than this temperature range, sufficient drying will not be possible, and instead of becoming powder-like, it will aggregate and become lump-like. The powdered non-rubber components obtained from the natural rubber latex serum of the present invention are synthetic rubber modifiers, vulcanization accelerators, coating agents for rubber reinforcing fillers, feeds,
It is industrially useful and can be used in pharmaceuticals, etc. An example of the details of the usefulness is given in the applicant's patent application published in 1983.
−136390 (Special Publication No. 02-55372), Patent Application 1983−
It is stated in No. 136392 (Special Publication No. 03-51737). <Example> A powdered non-rubber component was produced using the raw latex having the composition shown in Table 2 and according to the manufacturing method shown in Table 2. Table 3 shows the analysis results of proteins and amino acids contained in the powdered non-rubber component obtained in Example 5. The equipment used for the spray method was a nozzle type spray dryer: L-5 manufactured by Yamato Scientific Co., Ltd.
(DL-41) type, disk type spray dryer: L-12 type manufactured by Okawara Kakoki Co., Ltd. Non-rubber components (solids) were measured using a Kett automatic moisture meter. The viscosity was measured using a B-type viscometer. Separately, as a comparative example, the same raw material latex as used in Examples 4 and 5 was used and treated at the disk rotation speed and sample drying temperature shown in Table 2. The average particle diameter of the obtained samples of Examples and Comparative Examples,
The particle shape, moisture content, particle color, and particle condition were measured and are shown in Table 2. Moisture content was measured using a Kett automatic moisture meter.

【表】【table】

【表】【table】

【表】 第2表の実施例と比較例を参照して以下の事が
わかる。 (1) デイスク回転数が10000〜30000r.p.mの範囲
外では得られる非ゴム成分の形状がダンゴ状に
なつたり、又はドライヤー内壁に付着が多くな
る。 (2) 試料乾燥温度の入口及び出口温度が250℃/
130℃〜150℃/50℃外であると試料の熱変性が
おこつたり乾燥が不充分となる。 <発明の効果> 本発明の平均粒径10〜100μの天然ゴムラテツ
クス漿液から得られる粉末状の非ゴム成分は、合
成ゴム改質剤、加硫促進剤、ゴム補強性充填剤の
コーテイング剤、飼料、医薬品等に利用して工業
上有用であり、水や溶剤に溶解混合しやすく運搬
輸送に便利である。 本発明の天然ゴムラテツクス漿液から得られる
粉末状の非ゴム成分は所望の平均粒径で収率よく
製造することができる。 本発明の非ゴム成分を製造するに際し、スプレ
ードライを、試料入口乾燥温度150〜250℃、試料
出口温度50〜130℃のスプレードライ容器内への
スプレードライとし、回転数10000〜30000r.p.m
のデイスク回転体で行うか、あるいは吹出圧力
0.5〜2.0Kg/cm2のノズルによつて行えば、平均粒
径を10〜100μに制御することができ、得られる
製品粉末は吸湿・凝固しにくく、スプレードライ
ヤー内壁に付着することもないので、収率が良く
なる。また、工業的に利用する際に水や溶剤に溶
解しやすく、カサ比重が適切で運搬しやすいもの
となる。 さらに、従来天然ゴク製造時の廃棄物として環
境汚染による公害問題を引き起していた漿液中の
蛋白質、糖分、樹脂分等の非ゴム分を水と分離
し、利用価値の高い粉末状非ゴム成分として利用
できるため、公害問題が完全に解消し、省資源効
果が高く、ゴム工業の効率が上昇する。
[Table] The following can be understood by referring to the Examples and Comparative Examples in Table 2. (1) When the disk rotation speed is outside the range of 10,000 to 30,000 rpm, the shape of the obtained non-rubber component becomes lumpy, or it tends to adhere to the inner wall of the dryer. (2) Inlet and outlet temperature of sample drying temperature is 250℃/
If the temperature is outside 130°C to 150°C/50°C, thermal denaturation of the sample will occur and drying will be insufficient. <Effects of the Invention> The powdered non-rubber component obtained from the natural rubber latex serum having an average particle size of 10 to 100μ according to the present invention can be used as a synthetic rubber modifier, a vulcanization accelerator, a coating agent for rubber reinforcing fillers, and feed. It is industrially useful for use in medicines, etc., and is easy to dissolve and mix in water or solvents, making it convenient for transportation. The powdered non-rubber component obtained from the natural rubber latex serum of the present invention can be produced with a desired average particle size and with good yield. When producing the non-rubber component of the present invention, spray drying is performed in a spray drying container with a sample inlet drying temperature of 150 to 250°C, a sample outlet temperature of 50 to 130°C, and a rotation speed of 10,000 to 30,000 r.pm.
This can be done with a rotary disk or by blowing pressure.
By using a 0.5-2.0Kg/ cm2 nozzle, the average particle size can be controlled to 10-100μ, and the resulting product powder is difficult to absorb moisture and coagulate, and does not adhere to the inner wall of the spray dryer. , the yield will be better. In addition, when used industrially, it is easily dissolved in water or a solvent, has an appropriate bulk specific gravity, and is easy to transport. In addition, non-rubber components such as proteins, sugars, and resins in the serous fluid, which had traditionally caused pollution problems due to environmental pollution as waste during the production of natural goku, are separated from water, and a non-rubber powder with high utility value is produced. Since it can be used as a component, it completely eliminates pollution problems, has a high resource saving effect, and increases the efficiency of the rubber industry.

Claims (1)

【特許請求の範囲】 1 天然ゴムラテツクス中のゴム成分を凝固除去
した残りの漿液を150〜250℃の高温雰囲気中へス
プレードライし、水分を蒸発させて平均粒径10〜
100μの粉末状としてなることを特徴とする天然
ゴムラテツクス漿液から得られる粉末状非ゴム成
分。 2 前記スプレードライが試料入口乾燥温度150
〜250℃、試料出口温度50〜130℃のスプレードラ
イ容器内へのスプレードライである特許請求の範
囲第1項に記載の天然ゴムラテツクス漿液から得
られる粉末状非ゴム成分。 3 前記スプレードライの工程がデイスク回転体
を用いて行われデイスク回転体の回転数が10000
〜30000r.p.mである特許請求の範囲第1項または
第2項に記載の天然ゴムラテツクス漿液から得ら
れる粉末状非ゴム成分。 4 前記スプレードライの工程がノズルを用いて
行われノズルによる漿液の滴下がノズル吹出圧力
0.5〜2.0Kg/cm2である特許請求の範囲第1項また
は第2項に記載の天然ゴムラテツクス漿液から得
られる粉末状非ゴム成分。
[Claims] 1. The remaining serum after coagulating and removing the rubber components in natural rubber latex is spray-dried in a high-temperature atmosphere of 150 to 250°C to evaporate the moisture and reduce the average particle size to 10 to 250°C.
A powdery non-rubber component obtained from natural rubber latex serum, characterized in that it is in the form of a 100μ powder. 2 The spray drying is performed at a sample inlet drying temperature of 150°C.
The powdered non-rubber component obtained from natural rubber latex serum according to claim 1, which is spray-dried into a spray-drying container at a temperature of ~250°C and a sample outlet temperature of 50-130°C. 3. The spray drying step is performed using a disk rotating body, and the rotation speed of the disk rotating body is 10,000.
A powdered non-rubber component obtained from the natural rubber latex serum according to claim 1 or 2, wherein the natural rubber latex serum has a rotation rate of 30,000 rpm. 4 The spray drying process is performed using a nozzle, and the dripping of the serum by the nozzle is controlled by the nozzle blowing pressure.
The powdered non-rubber component obtained from the natural rubber latex serum according to claim 1 or 2, which has a weight of 0.5 to 2.0 Kg/cm 2 .
JP60136391A 1985-06-22 1985-06-22 Powdered nonrubber component obtained from serum of natural rubber latex and production thereof Granted JPS61293201A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP60136391A JPS61293201A (en) 1985-06-22 1985-06-22 Powdered nonrubber component obtained from serum of natural rubber latex and production thereof
GB8614585A GB2178045B (en) 1985-06-22 1986-06-16 Particulate nonrubber materials derived from serums resulting from treatment of natural rubber latexes and method of their production
IDP287486A ID805B (en) 1985-06-22 1986-06-20 PARTICLE MATERIAL IS NOT RUBBER LOWERED FROM SERUM RESULTS OF NATURAL RUBBER PROCESSING AND ITS PRODUCT METHOD
CN86104275A CN1011860B (en) 1985-06-22 1986-06-21 Non-rubber pellets made from a slurry remaining after processing natural rubber latex and process for producing the same
MYPI87000097A MY102130A (en) 1985-06-22 1987-02-05 Particulate nonrubber materials derived from serums resulting from treatment of natural rubber latexes and method of their production.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60136391A JPS61293201A (en) 1985-06-22 1985-06-22 Powdered nonrubber component obtained from serum of natural rubber latex and production thereof

Publications (2)

Publication Number Publication Date
JPS61293201A JPS61293201A (en) 1986-12-24
JPH0380801B2 true JPH0380801B2 (en) 1991-12-26

Family

ID=15174061

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60136391A Granted JPS61293201A (en) 1985-06-22 1985-06-22 Powdered nonrubber component obtained from serum of natural rubber latex and production thereof

Country Status (5)

Country Link
JP (1) JPS61293201A (en)
CN (1) CN1011860B (en)
GB (1) GB2178045B (en)
ID (1) ID805B (en)
MY (1) MY102130A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6582728B1 (en) 1992-07-08 2003-06-24 Inhale Therapeutic Systems, Inc. Spray drying of macromolecules to produce inhaleable dry powders
ATE416755T1 (en) 1994-03-07 2008-12-15 Nektar Therapeutics METHOD AND COMPOSITION FOR PULMONARY ADMINISTRATION OF INSULIN
US6740719B1 (en) 1998-03-18 2004-05-25 George W. Weinert Process for reducing protein allergens in latex products
US20110250264A1 (en) 2010-04-09 2011-10-13 Pacira Pharmaceuticals, Inc. Method for formulating large diameter synthetic membrane vesicles
EP3257574A1 (en) * 2016-06-15 2017-12-20 Clariant International Ltd Method for producing a particle-shaped material
MY197240A (en) * 2016-09-02 2023-06-07 Thailand Center Of Excellence For Life Sciences Method for preparing an extract of hevea latex and composition thereof

Also Published As

Publication number Publication date
GB2178045A (en) 1987-02-04
MY102130A (en) 1992-04-30
GB2178045B (en) 1989-07-12
GB8614585D0 (en) 1986-07-23
JPS61293201A (en) 1986-12-24
CN86104275A (en) 1987-01-21
CN1011860B (en) 1991-03-06
ID805B (en) 1996-07-11

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