JPS587647B2 - Hannobutsu o Renzokutekininoushiyuku Sasenagara Oshidastameno Souchi - Google Patents
Hannobutsu o Renzokutekininoushiyuku Sasenagara Oshidastameno SouchiInfo
- Publication number
- JPS587647B2 JPS587647B2 JP5383473A JP5383473A JPS587647B2 JP S587647 B2 JPS587647 B2 JP S587647B2 JP 5383473 A JP5383473 A JP 5383473A JP 5383473 A JP5383473 A JP 5383473A JP S587647 B2 JPS587647 B2 JP S587647B2
- Authority
- JP
- Japan
- Prior art keywords
- screw shaft
- product
- resin
- reaction
- screw shafts
- 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
Links
- 238000010438 heat treatment Methods 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 239000011134 resol-type phenolic resin Substances 0.000 claims description 3
- 238000005086 pumping Methods 0.000 claims description 2
- 229920005989 resin Polymers 0.000 description 31
- 239000011347 resin Substances 0.000 description 31
- 239000000047 product Substances 0.000 description 27
- 238000006243 chemical reaction Methods 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 229920003987 resole Polymers 0.000 description 8
- 229910021529 ammonia Inorganic materials 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000009833 condensation Methods 0.000 description 5
- 238000005192 partition Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- HSRJKNPTNIJEKV-UHFFFAOYSA-N Guaifenesin Chemical compound COC1=CC=CC=C1OCC(O)CO HSRJKNPTNIJEKV-UHFFFAOYSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007931 coated granule Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 235000012438 extruded product Nutrition 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- -1 methylol groups Chemical group 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 239000003110 molding sand Substances 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
Landscapes
- Phenolic Resins Or Amino Resins (AREA)
Description
【発明の詳細な説明】
この発明は反応樹脂生成物の濃縮に好適であり、とくに
シエルモールド用鋳型または中子の製造にもつとも適し
た自己縮合性を有する樹脂の連続濃縮装置に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an apparatus for continuously concentrating a resin having self-condensing properties, which is suitable for concentrating reaction resin products, and particularly suitable for producing molds or cores for shell molds.
成形材料のために、もしくは耐火性粒状物を被覆するた
めに、またはとくに鋳型用砂粒を被覆するためにレゾー
ル型フェノール樹脂を用いることはすでに提案されてい
る。It has already been proposed to use resol-type phenolic resins for molding materials or for coating refractory granules or, in particular, for coating molding sand grains.
一般にレゾール型フェノール樹脂とは、フェノール類1
モルに対してホルムアルデヒド類1モル以上を使用し、
アルカリ性触媒の存在下でこれらを反応させて得られる
樹脂をいい、該樹脂はアルカリ金属の水酸化物等を触媒
として得られる通常レゾールと呼ばれる樹脂と、アンモ
ニアまたは第1級アミン、第2級アミン等を触媒として
得られるアンモニアレゾールと呼ばれる樹脂とに大別さ
れる。In general, resol type phenolic resin refers to phenols 1
Using 1 mol or more of formaldehyde per mol,
A resin obtained by reacting these in the presence of an alkaline catalyst, and the resin is a resin obtained by using an alkali metal hydroxide as a catalyst, usually called a resol, and ammonia, a primary amine, or a secondary amine. It is broadly divided into resins called ammonia aresols, which are obtained using ammonia and the like as catalysts.
前記レゾールは粘稠な液体として得られるもので、水溶
性もしくは親水性を有し、アルコール、アセトン等の有
機溶剤に可溶で、一般にフェスとして使用される。The resol is obtained as a viscous liquid, is water-soluble or hydrophilic, and is soluble in organic solvents such as alcohol and acetone, and is generally used as a face.
一方、前記アンモニアレゾールは粘稠な液体として得ら
れるだけでなく、条件次第では固体状生成物として得ら
れることが特徴で、疎水性を有しアルコール、アセトン
等の有機溶剤に可溶である。On the other hand, the ammonia aresol is characterized in that it can be obtained not only as a viscous liquid but also as a solid product depending on the conditions, and is hydrophobic and soluble in organic solvents such as alcohol and acetone.
液状のものに比べて上記のような固形レゾールがとくに
有用である点は、固形状であるために取扱いがきわめて
容易なことであり、貯蔵安定性にすぐれていることであ
る。Compared to liquid resols, solid resols as described above are particularly useful in that they are extremely easy to handle and have excellent storage stability.
しかしながら固形状アンモニアレゾールはその製造に際
し、つぎのような著しい困難性がある。However, solid ammonia aresol has the following significant difficulties in its production.
すなわち自己縮合性を有するため、固形状になるまで加
熱反応を行なうと連鎖反応的に縮合が進み、反応の制御
がきわめて難しくなることである。That is, since it has self-condensing properties, if a heating reaction is carried out until it becomes a solid state, condensation proceeds like a chain reaction, making it extremely difficult to control the reaction.
また、大量生産する場合反応容器は一般に3000〜I
OOOOJの容量のものを使用するが、100℃付近に
まで加熱反応を行なったのち、iooo〜4000Jの
樹脂を、自己縮合反応が起らない温度(約30℃)まで
数分間以内に同時に急冷することは工業的に全く不可能
に近い。In addition, for mass production, the reaction container is generally 3000~I
A resin with a capacity of OOOOJ is used, but after heating the reaction to around 100℃, the resin of iooo~4000J is simultaneously rapidly cooled within a few minutes to a temperature at which the self-condensation reaction does not occur (approximately 30℃). This is almost impossible industrially.
すなわち、樹脂物は一般に断熱性を有し、外部よりの冷
却方法では樹脂物の内部まで冷却することが不可能であ
り、内部では自己縮合が進み、爆発的に発熱反応を誘起
して硬化する。In other words, resin materials generally have heat insulating properties, and it is impossible to cool the inside of the resin material using external cooling methods, and self-condensation progresses inside, causing an explosive exothermic reaction and hardening. .
前記したように固形レゾールを製造するには種種困難を
ともなうが、さらに樹脂の被覆性および貯蔵安定性を確
保するために水分を含まない固形状レゾールを得ること
もまたきわめて困難とされていた。As mentioned above, there are various difficulties involved in producing solid resols, but it has also been extremely difficult to obtain solid resols that do not contain water in order to ensure coating properties and storage stability of the resin.
すなわち、常圧下、高温雰囲気によって単純に反応物中
の水分除去を試みたとしても、かかる温度上昇によって
樹脂の反応がさらに助長される結果、メチロール基の量
は急激に低下し、被覆粒状物の硬化速度は遅《なり、粘
結強度も極度に悪化することをまぬがれないからである
。In other words, even if an attempt is made to simply remove water from the reactants in a high-temperature atmosphere under normal pressure, the reaction of the resin will be further promoted by such a rise in temperature, resulting in a rapid decrease in the amount of methylol groups and the formation of coated granules. This is because the curing speed becomes slow and the caking strength inevitably deteriorates extremely.
古くより知られているいくつかのフェノール樹脂連続製
造方法は、いずれもノボラック型樹脂のものであり、自
己縮合性を有するレゾール型樹脂は一般にバッチシステ
ムで製造されていた。Several methods for continuously producing phenolic resins that have been known for a long time are all for novolac type resins, and resol type resins having self-condensing properties have generally been manufactured in a batch system.
近次スプレードライ方法によるレゾール型樹脂の製造も
行なわれてはいるが、この方法は、塔の最上部よりレゾ
ール樹脂の一定反応生成物を噴霧する方法であり、水分
の除去には一応効果的ではあるが、応用製品に最適の軟
化点を有する固形状レゾールを得るためには、噴霧乾燥
塔内部の温度調整がきわめて困難となる欠点がある。Although resol-type resins have recently been produced by spray-drying, this method involves spraying a certain reaction product of resol resin from the top of a tower, and is somewhat effective in removing water. However, it has the disadvantage that it is extremely difficult to adjust the temperature inside the spray drying tower in order to obtain a solid resol with an optimal softening point for applied products.
すなわち、塔の高さに制限をうけ、霧状樹脂の自然落下
中においてその反応を調節することはまさに至難の技と
いえよう。In other words, it is extremely difficult to control the reaction of atomized resin as it falls naturally due to the height of the tower.
本発明の目的は、従来技術に内在する上記のような種々
の欠点を削除し、定量連続的に加熱反応を行ないながら
所望の性状の樹脂とくに自己縮合性を有する固形レゾー
ルを製造するのに適した装置を提供することである。The purpose of the present invention is to eliminate the various drawbacks inherent in the prior art as described above, and to make the present invention suitable for producing resins with desired properties, particularly solid resols having self-condensing properties, while carrying out quantitative continuous heating reactions. The objective is to provide a device with
すなわち本発明の特徴とするところは、前述したように
大量の樹脂生成物を同時に所望の程度まで反応を進めて
しまうのでなく、単位時間当り容易に急冷可能な量の樹
脂生成物が、移送されながら順次連続して反応を進めら
れ、排出時点において前記反応が所望の程度に過不足な
く達するようたとえば生成物の送りに使用されるねじ軸
のトルク変動を検出してその限界により送り速度が制御
されることである。In other words, the feature of the present invention is that instead of simultaneously proceeding the reaction of a large amount of resin product to a desired degree as described above, an amount of resin product that can be easily quenched per unit time is transferred. For example, the torque fluctuation of the screw shaft used to feed the product is detected and the feed rate is controlled based on the limit, so that the reaction progresses one after another and the reaction reaches the desired degree at the time of discharge. It is to be done.
なぜならば反応の程度が不十分であれば求めるような樹
脂の軟化点が得られず、逆に過度となれば生成物のゲル
化をともなって装置自体の機能が停止することも起りう
るからである。This is because if the degree of reaction is insufficient, the desired softening point of the resin cannot be obtained, and if the degree of reaction is excessive, the product may gel and the function of the device itself may stop. be.
また、本装置に供給されるレゾール樹脂の一定反応生成
物は、なお15%程度の水分を含有するため反応の進行
と並行して蒸発、積極脱水を行ないながら、しかも移送
順序を乱さないようにピストンフローさせることである
。In addition, since the certain reaction product of the resol resin supplied to this device still contains about 15% water, it is necessary to evaporate and actively dehydrate it in parallel with the progress of the reaction, without disturbing the transfer order. The goal is to make the piston flow.
さらに、上記積極脱水にもとずく負圧の影響樹脂の押し
出しを阻害するので、これを防ぐため、濃縮工程の末期
に前記ねじ軸の可変ピッチによる樹脂の圧縮作用部分が
付加されていることである。Furthermore, since the influence of negative pressure based on the above-mentioned active dehydration inhibits the extrusion of the resin, in order to prevent this, a compressing part of the resin is added by the variable pitch of the screw shaft at the end of the concentration process. be.
以下に図面に示したこの発明の好適な実施例装置につい
て詳しく説明する。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS A preferred embodiment of the present invention shown in the drawings will be explained in detail below.
図において、1,1′は並列しで横設され、かつ左右1
対の、リードを有して噛み合わされたねじ軸で、密封中
空状の内孔2,2′,を有し、両端に支軸部3,4,3
’,4’をそれぞれ延出せしめている。In the figure, 1 and 1' are installed horizontally in parallel, and one on the left and one
A pair of screw shafts that are engaged with each other with leads, and have sealed hollow inner holes 2, 2', and support shaft portions 3, 4, 3 at both ends.
', 4' are extended respectively.
5はねじ軸1,1′を密封する筒体であって、その内壁
はねじ軸1,1′の終端部外径とのみ密合する部分6を
もち、他の部分はねじ軸外径上方に排気室7を形成して
いる。Reference numeral 5 denotes a cylindrical body that seals the screw shafts 1, 1', and its inner wall has a portion 6 that fits only with the outer diameter of the terminal end of the screw shafts 1, 1', and the other portions are located above the outer diameter of the screw shafts. An exhaust chamber 7 is formed in the exhaust chamber 7.
この排気室7は可塑状物の移送水準を最高に保つために
前記ねじ軸1,1′の谷径上縁8を下限水準(ねじ軸外
径から離れて排気室を形成する筒体内壁の最下位置)と
してきめられている。In order to maintain the transfer level of the plastic material at the highest level, this exhaust chamber 7 is designed so that the upper edge 8 of the root diameter of the screw shafts 1, 1' is set at a lower limit level (the inner wall of the cylinder forming the exhaust chamber away from the outer diameter of the screw shaft). (lowest position).
9,91ま支軸部3,3′に嵌合連結された替えねじで
あって、筒体5の前記部分6と嵌合する前記ねじ軸終端
部のさらに限られた端末部分を形成し、そのねじ山ピソ
チは他の部分のそれよりも小さく設定されている。9 and 91 are replacement screws that are fitted and connected to the support shaft portions 3 and 3', forming a further limited terminal portion of the screw shaft terminal portion that fits into the portion 6 of the cylinder body 5; Its thread pitch is set smaller than that of other parts.
10,11は端壁であって筒体50両端部を封塞すると
同時にねじ軸1,1′および9,9′の終始端面と摺接
し、かつねじ軸9,9′の終端面における下方噛み合い
点12の近傍と対向する位置には側壁10を貫通する排
出口が設けてあり、これより排出管13が突出延在して
いる。Reference numerals 10 and 11 denote end walls which close both ends of the cylindrical body 50 and at the same time make sliding contact with the terminal end surfaces of the screw shafts 1, 1' and 9, 9', and engage downwardly at the terminal surfaces of the screw shafts 9, 9'. A discharge port passing through the side wall 10 is provided at a position opposite to the vicinity of the point 12, from which a discharge pipe 13 protrudes and extends.
14は筒体5の外郭を覆う被套でねじ軸1,1′の長手
方向に隔壁15で相互に区画された独立室I,■,■,
■,Vをもち、これらの各室は制御された加熱媒体たと
えば蒸気の出入を許す入口16および出口17を開口し
ている。14 is a sheath that covers the outer shell of the cylinder 5, and has independent chambers I, ■, ■, separated from each other by partition walls 15 in the longitudinal direction of the screw shafts 1 and 1'.
(1), V, and each of these chambers opens with an inlet 16 and an outlet 17 allowing controlled entry and exit of a heating medium, such as steam.
なお18は加熱媒体を効率よく案内するために各独立室
ごとに複列的に配設された仕切壁であって、前記両隔壁
15との接合部分が交互に切り欠かれて通路19を形成
している。Reference numeral 18 denotes partition walls arranged in double rows for each independent chamber in order to guide the heating medium efficiently, and passages 19 are formed by alternately cutting out the joints with both partition walls 15. are doing.
20〜22はいずれも排気室7を形成する筒体5に貫設
された開口であって、20は図示しない原料供給管と連
結した1対の受入口、21は図示しない減圧装置と連結
した吸気口、22は覗き窓である。Reference numerals 20 to 22 are all openings formed through the cylindrical body 5 forming the exhaust chamber 7, 20 is a pair of intake ports connected to a raw material supply pipe (not shown), and 21 is connected to a pressure reducing device (not shown). The intake port 22 is a viewing window.
23,23’lま回転接手24,24’に支持され、ね
じ軸1,1′の前記支軸部3,3′を貫通して前記内孔
2,2′内にそれぞれ延出している中空状の加熱管で、
周壁の適数箇所に加熱媒体たとえば蒸気の噴出孔25を
貫設し、かつ凝縮水を排出するために先端に吸水ノズル
27,27’を備えた吸水管26を同軸的に内蔵してい
る。23, 23'l are supported by rotary joints 24, 24', and extend through the support shaft portions 3, 3' of the screw shafts 1, 1' into the inner holes 2, 2', respectively. With a shaped heating tube,
Jet holes 25 for a heating medium, such as steam, are provided through the circumferential wall at appropriate locations, and a water suction pipe 26 having water suction nozzles 27, 27' at its tip for discharging condensed water is coaxially built therein.
なお、28は原動機付変速機、29は減速機、30は歯
車箱、31はねじ軸1,1′の支軸部4,4′をそれぞ
れ支承する軸受、32,32’は同じく支軸部3,3′
をそれぞれ支承する軸受、33は被套14の下底部に貫
設した凝縮水の排出孔である6本発明装置によって濃縮
される可塑状物たとえばレゾール樹脂の一定反応生成物
は、反応容器中においてフェノール類1モルとホルムア
ルデヒド類1〜3モルとを触媒量におけるアンモニアも
しくはアミン類の存在下、70℃!約60、.分間付加
反応させ、ついで減圧下に反応物が70℃を越えないよ
うに注意しながら反応物中の水分を除去して得られるほ
ぼ透明な生成物である。In addition, 28 is a motorized transmission, 29 is a speed reducer, 30 is a gear box, 31 is a bearing that supports the support shafts 4 and 4' of the screw shafts 1 and 1', respectively, and 32 and 32' are the support shafts. 3,3'
33 is a condensed water discharge hole penetrated through the lower bottom of the jacket 14. 6 A certain reaction product of a plastic material such as a resol resin is concentrated by the apparatus of the present invention, and phenol is 1 mole of formaldehyde and 1 to 3 moles of formaldehyde at 70°C in the presence of a catalytic amount of ammonia or amines! Approximately 60. This is an almost transparent product obtained by allowing the addition reaction to occur for a minute, and then removing water from the reaction mixture under reduced pressure while being careful not to exceed 70°C.
上記生成物が直接にか、もしくは貯留容器を経て前記受
入口20から導入される。The product is introduced through the inlet 20 either directly or via a storage vessel.
生成物の単位時間当りの導入流量は、所望製品の性状に
もとづいて定められるねじ軸1,1′の回転速度に応じ
、生成物の筒体内水準が前記ねじ軸の谷径上縁8を越え
ないように制御される。The introduction flow rate of the product per unit time is determined according to the rotational speed of the screw shafts 1, 1', which is determined based on the properties of the desired product, until the level of the product inside the cylinder exceeds the upper edge 8 of the root diameter of the screw shaft. controlled so that it does not occur.
ねじ軸1,1′は生成物の圧送を主目的として、それぞ
れが外回り方向に緩速度たとえば毎時20〜70回転程
度で運転される。The screw shafts 1, 1' are each operated in an outward direction at a slow speed, for example, about 20 to 70 revolutions per hour, with the main purpose of pumping the product under pressure.
受入口20から導入された生成物は、ねじ軸1,1′と
筒体5との間でねじ山の1ピッチごとにほぼ隔絶した状
態で移送され、その間被套14および加熱管23,23
’に供給される加熱媒体によって加熱が行なわれ、縮合
の進行にともなう縮合水は、前記吸気口27,27’と
連結した減圧装置により積極的に除去される。The product introduced from the receiving port 20 is transferred between the screw shafts 1, 1' and the cylinder 5 in a state where they are separated by almost every pitch of the screw thread, while the product is transferred to the sheath 14 and the heating tubes 23, 23.
Heating is carried out by the heating medium supplied to the inlets 27, 27', and condensed water as the condensation progresses is actively removed by a pressure reducing device connected to the inlet ports 27, 27'.
加熱温度は隔壁15で区画された各独立室I,■,■,
■,Vごとに制御され、それにより生成物が筒体5の部
分6と密合するねじ軸終端部に到達するまでに約70℃
〜105℃にと昇温され、その後、前記ねじ軸1,1′
と筒体5との密合によって、生成物は減圧装置の影響域
から離れて密送段階へと移行する。The heating temperature is determined in each independent chamber I, ■, ■, divided by partition wall 15.
■, by the time the product reaches the end of the screw shaft where it comes into close contact with the part 6 of the cylinder 5, it is approximately 70°C.
The temperature is raised to ~105°C, and then the screw shafts 1, 1'
Due to the close contact between the cylinder 5 and the cylinder 5, the product leaves the area of influence of the pressure reducing device and passes into the conveying stage.
この段階では生成物自体の反応熱が高いため、加熱管2
3,23’による補助加熱の影響をむしろ避けるように
、ねじ軸1,1′は中実状に形成されている。At this stage, the reaction heat of the product itself is high, so the heating tube 2
The screw shafts 1, 1' are formed solid so as to avoid the influence of auxiliary heating caused by the screws 3, 23'.
縮合水の除去によって幾分水準の低下した生成物が、前
記ねじ軸終端部のさらに限られた端末部分へと移動した
時点では、生成物の温度は約110℃〜120℃の臨界
温度に達して所望の程度にまで反応が進み、さらに替え
ねじ9,9′の可変ピッチによって急激に圧縮され、生
成物の水準は上昇してねじ山間の空隙を完全に充足する
。When the product, whose level has been reduced somewhat by the removal of condensation water, has moved to a more limited end portion of the screw shaft end, the temperature of the product reaches a critical temperature of about 110° C. to 120° C. When the reaction proceeds to the desired extent, it is further rapidly compressed by the variable pitch of the replacement screws 9, 9', and the level of product rises to completely fill the void between the screw threads.
ねじ軸9,9′の終端面が側壁10と摺接して当該箇所
に生成物排出のためのチャンバが設けられていないのも
本発明の利点の1つであって、生成物は上記チャンバ内
で生ずる乱流の懸念もなく、したがって熟成の順序を全
く崩すことなく、しかも圧縮の極限位置に相当するねじ
軸1,1′の下方噛合点12の近傍から排出管13を通
って強力に押し出される。One of the advantages of the present invention is that the end surfaces of the screw shafts 9, 9' are in sliding contact with the side wall 10, and no chamber is provided at that location for discharging the product. There is no fear of turbulence caused by the process, and therefore the aging order is not disrupted at all, and moreover, it is forcefully extruded through the discharge pipe 13 from the vicinity of the lower engagement point 12 of the screw shafts 1, 1', which corresponds to the extreme position of compression. It will be done.
押し出された生成物の粘度は約1000〜1200セン
チポイズであり、直ちに水中に導かれて引き上げられる
か、または無端搬送帯上で給水を受ける等図示しない任
意の冷却手段によって急冷固化せしめられ、固形レゾー
ル樹脂が得られる。The extruded product has a viscosity of approximately 1,000 to 1,200 centipoise, and is immediately introduced into water and pulled up, or rapidly cooled and solidified by any cooling means (not shown), such as receiving water on an endless conveying belt, to form a solid resol. Resin is obtained.
全濃縮工程の所要時間は40分程度であるが、樹脂の軟
化点は無段変速機28によるねじ軸1,1′の回転速度
ならびに外套14および加熱管23,23’に供給され
る加熱媒体の調節によって適確に制御される。The time required for the entire concentration process is about 40 minutes, but the softening point of the resin depends on the rotational speed of the screw shafts 1, 1' by the continuously variable transmission 28 and the heating medium supplied to the jacket 14 and heating tubes 23, 23'. is precisely controlled by adjusting the
なお、上記の実施例では2個のねじ軸1,1′を噛み合
わせた場合について説明したが、生産量に応じて3個以
上のねじ軸を並列して噛み合わせた構造のものにするこ
とも可能である。In the above embodiment, the case where two screw shafts 1 and 1' are meshed is explained, but depending on the production volume, a structure in which three or more screw shafts are meshed in parallel may be used. is also possible.
以上、詳述した本発明装置によれば、つぎのような幾多
の効果を奏する。According to the apparatus of the present invention described in detail above, the following numerous effects can be achieved.
(1)定量連続的に樹脂生成物の濃縮を進めながら、そ
の間の反応温度および反応時間を如何ようにも制御しう
るので、要求性状に適合した樹脂生成物をきわめて容易
に製造することができる。(1) Since the reaction temperature and reaction time can be controlled in any way while continuously concentrating the resin product quantitatively, it is possible to produce resin products that meet the required properties extremely easily. .
(2)導入順序を全く乱すことなく、連続的に排出され
るので、製造された樹脂生成物が著しく均質である。(2) The produced resin product is extremely homogeneous since it is discharged continuously without any disturbance in the order of introduction.
(3)濃縮の工程中に減圧脱水が行なわれるので樹脂生
成物の縮合水を効果的に除去することができる。(3) Since vacuum dehydration is performed during the concentration step, water of condensation from the resin product can be effectively removed.
(4)筒内の負圧に打ち勝つようにねじ軸にポンプ作用
を与え、しかもねじ軸の下方噛合点付近から生成物を押
し出すのでポンプ作用が一層効率的である。(4) A pump action is applied to the screw shaft so as to overcome the negative pressure in the cylinder, and the pump action is more efficient because the product is pushed out from near the lower meshing point of the screw shaft.
(5)ねじ軸の谷径上縁を吸気室の下限水準としている
ので、濃縮工程中、生成物の逆戻りを許さない範囲内で
生産量を最犬に維持することができる。(5) Since the upper edge of the valley diameter of the screw shaft is set as the lower limit level of the suction chamber, during the concentration process, the production amount can be maintained at the highest level within a range that does not allow the product to return.
図面は本発明の好適なひとつの実施例を例示したもので
あり、第1図は本発明装置の要部を切断した平面図、第
2図は第3図の■−W線に沿って切断した縦断面図、第
3図は第2図の■一一に沿って切断した横断面、第4図
は第2図の■−w’線に沿って切断した横断面図である
。
これらの図において、1,1′はねじ軸、2,2′はね
じ軸の内孔、3,3’,4,4’は支軸部、5は筒体、
10,11は端壁、13は排出管、14は被套、15は
隔壁、16は入口、17は出口、20は受入口、21は
吸気口、20〜22は開口、23,23’は加熱管、2
4,24’は回転接手、25は噴出孔、26は吸水管、
27,27’は吸水ノズル、28は原動機付変速機、2
9は減速機、30は歯車箱、31は軸受、32,32’
は軸受、33は排出孔。The drawings illustrate one preferred embodiment of the present invention, and FIG. 1 is a plan view of the main parts of the device of the present invention, and FIG. 2 is a cut along the line ■-W in FIG. 3. FIG. 3 is a cross-sectional view taken along line 2-11 in FIG. 2, and FIG. 4 is a cross-sectional view taken along line 2-w' in FIG. In these figures, 1 and 1' are screw shafts, 2 and 2' are inner holes of the screw shafts, 3, 3', 4, and 4' are support shaft parts, 5 is a cylinder body,
10 and 11 are end walls, 13 is a discharge pipe, 14 is a jacket, 15 is a partition wall, 16 is an inlet, 17 is an outlet, 20 is an intake port, 21 is an intake port, 20 to 22 are openings, 23 and 23' are heating tube, 2
4, 24' are rotating joints, 25 is a spout hole, 26 is a water suction pipe,
27, 27' are water absorption nozzles, 28 is a motorized transmission, 2
9 is a reducer, 30 is a gear box, 31 is a bearing, 32, 32'
is a bearing, and 33 is a discharge hole.
Claims (1)
個のねじ軸と、前記ねじ軸を密封し、かつ内壁がねじ山
ピツチが他の部分のそれよりも小さく設定されたねじ軸
の終端部外径とのみ密合せられ他の部分はねじ軸外径上
方において排気室を形成するとともにその終端部側壁に
はねじ軸の下方噛み合い点近傍との対向位置に前記可塑
状物の排出口が貫設されている筒体と、前記排気室と連
結せられた減圧装置と、前記筒体の外郭を覆い前記ねじ
軸の長手方向に区画された独立室がそれぞれ加熱給源と
連結された被套とを包含し反応生成物を連続的に濃縮さ
せながら押し出すことを特徴とするレゾール型フェノー
ル樹脂の製造装置。1 at least two meshed together for pumping plastic material
The screw shaft is sealed, and the inner wall is tightly fitted only with the outer diameter of the terminal end of the screw shaft whose thread pitch is set smaller than that of other parts, and the other parts are outside the screw shaft. A cylindrical body which forms an exhaust chamber in the radial upper part and has a discharge port for the plastic material penetrated through the end side wall thereof at a position opposite to the vicinity of the lower engagement point of the screw shaft, and is connected to the exhaust chamber. a depressurizing device, which covers the outer shell of the cylindrical body, and an independent chamber partitioned in the longitudinal direction of the screw shaft, each of which is connected to a heating source, and extrudes the reaction product while continuously concentrating it. A resol-type phenolic resin manufacturing device characterized by:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5383473A JPS587647B2 (en) | 1973-05-15 | 1973-05-15 | Hannobutsu o Renzokutekininoushiyuku Sasenagara Oshidastameno Souchi |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5383473A JPS587647B2 (en) | 1973-05-15 | 1973-05-15 | Hannobutsu o Renzokutekininoushiyuku Sasenagara Oshidastameno Souchi |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS503469A JPS503469A (en) | 1975-01-14 |
| JPS587647B2 true JPS587647B2 (en) | 1983-02-10 |
Family
ID=12953808
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5383473A Expired JPS587647B2 (en) | 1973-05-15 | 1973-05-15 | Hannobutsu o Renzokutekininoushiyuku Sasenagara Oshidastameno Souchi |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS587647B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5243865A (en) * | 1975-10-03 | 1977-04-06 | Japan Steel Works Ltd | Method of degassing material of volatile contained material degassing biaxial extruder and degassing biaxial extruder |
-
1973
- 1973-05-15 JP JP5383473A patent/JPS587647B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS503469A (en) | 1975-01-14 |
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