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JPH0122815B2 - - Google Patents
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JPH0122815B2 - - Google Patents

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Publication number
JPH0122815B2
JPH0122815B2 JP56030504A JP3050481A JPH0122815B2 JP H0122815 B2 JPH0122815 B2 JP H0122815B2 JP 56030504 A JP56030504 A JP 56030504A JP 3050481 A JP3050481 A JP 3050481A JP H0122815 B2 JPH0122815 B2 JP H0122815B2
Authority
JP
Japan
Prior art keywords
oil
membrane
pulp
adsorbent
regeneration
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP56030504A
Other languages
Japanese (ja)
Other versions
JPS57147436A (en
Inventor
Akira Hamada
Keiichi Oohira
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.)
Kureha Corp
Original Assignee
Kureha Corp
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 Kureha Corp filed Critical Kureha Corp
Priority to JP3050481A priority Critical patent/JPS57147436A/en
Priority to GB8115441A priority patent/GB2080350A/en
Priority to DE19813120531 priority patent/DE3120531A1/en
Priority to FR8110276A priority patent/FR2482867A1/en
Publication of JPS57147436A publication Critical patent/JPS57147436A/en
Publication of JPH0122815B2 publication Critical patent/JPH0122815B2/ja
Granted legal-status Critical Current

Links

Classifications

    • 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
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/74Recovery of fats, fatty oils, fatty acids or other fatty substances, e.g. lanolin or waxes

Landscapes

  • Fats And Perfumes (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
  • Filtering Materials (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Description

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

本発明は食用油再生用膜に係わるものであり、
特に揚げ油などの劣化により生成した不純物を吸
着および過し、揚げ油を再生するための家庭用
乃至小型業務用の食用油再生用膜に係る。 天婦羅、フライ等の揚げ物に使用した食用油は
酸化、重合などの化学的変化を受けて劣化が生ず
るのみならず、例えば魚、肉、野菜などの揚物材
料から臭気が移行するため、揚油を繰り返し使用
する場合は調理品の味覚が損なわれる。 従来、上述した如き劣化成分を含む揚油を再生
するための市販の家庭用食用油の再生装置は揚油
即ち使用済み食用油中に混入された固形物の過
を主とするもので、油の変質は主として油中に溶
解した熱酸化、熱重合、熱分解、加水分解などに
よる各種の変質や劣化成分、微細粒子状の生成物
や臭気は殆んど除去されない欠陥がある。微細粒
子自身が過熱されて分解し、その分解物が着色な
どの揚油の変質に影響を与えるものである。 本発明者等は、揚油の再生について種々検討を
行なつた結果、活性白土とパルプからなる主とし
てカツプ状の食用油再生用膜を吸着材として適
用することによつて、揚油中の劣化成分は実質的
に吸着除去され、殆んど使用前の油と変らぬ状態
にまで再生されることを見出し、特願昭55−
68495号および特願昭55−130462号の発明を行な
つた。 これらの場合吸着剤としては活性白土および酸
性白土などは吸着効果が最も優れ、劣化油の脱
色、脱臭、脱泡、脱煙等の点で優れた吸着特性を
示すものであるが、その反面吸着剤自体の僅かな
臭気、即ち一般に粘土臭、白土臭などといわれる
ものが揚物および食用油中に移行して天婦羅やフ
ライの味覚を損なう場合があり、活性白土におい
ては特に硫黄臭を伴なう場合があり再生用膜を用
いる精製法も未だ不満足であつた。 本発明者等は更に鋭意研究の結果、活性白土中
の酸性成分をアルカリ性物質により処理してなる
改質吸着剤とパルプから食用油再生用膜を製造す
ることにより上述した問題を解決し、粉状の微粉
体を添加する必要もなく、従つて撹拌操作を行な
わなくとも食用油の精製が可能となり、活性白土
土の悪臭とも言われる白土臭等のない再生油が得
られることを見出した。 周知の如く食用油は粘度が高く、常温では紙
又は布の如き膜状材による過速度は極めて
遅いが、高温では粘度が下り過速度が速くな
る。一方油の吸着精製は高温になる程効果的に行
なわれる。 本発明者等は、特願昭55−68495号によりこの
温度上昇による吸着精製速度の向上が過速度の
上昇よりも効果的であるので、調理に使用された
直後の加熱された油は吸着剤を膜状に成形した層
を一回通過させるだけで充分に精製されることを
見出し、吸着剤を膜状に成形し材とすることお
よびその膜をカツプ状とすれば最も都合のよいこ
とを見出している。 本発明は特願昭55−68495号で使用される再生
用膜に用いる吸着剤を活性白土をアルカリ性物質
を用いて処理したものを使用することを特徴とす
るものであるが、その形態はカツプ状に限らず本
来のシート状のもの迄も含むようにしたものであ
る。 本発明はパルプ5〜95重量部およびアルカリ性
物質を用いて処理して得られた95〜5重量部から
なる層を1層以上含む食用油再生用膜である。こ
の膜上に天婦羅に使用して劣化した油を入れる
と、油は多孔質の層を浸透して過され、この
過中に油中の劣化成分や臭気着色などが吸着され
ると共に、油中の揚げかすや炭化物などの固形物
も別され、白土臭のない精製された油が液と
して得られるものである。 本発明において使用する吸着剤としては、活性
白土中の酸性成分をアルカリ性物質により処理し
てなる多孔性の無機質の固体吸着剤を主とするも
のであり、単独又は2種以上が使用される。顆粒
および粉体の吸着剤の粒径は特に限定するもので
はないが、通常500μ以下の粒径のものが好まし
い。 本発明において使用するアルカリ性物質は食品
衛生上許可されており、改質剤中に微量含有され
ても安全なものであり、例えば炭酸ソーダ、炭酸
水素ナトリウム、苛性ソーダ、ピロ燐酸ソーダ、
消石灰、生石灰、酸化カルシウム、炭酸カルシウ
ムその他の公知の無機質アルカリ性物質であり、
単独又は2種以上の併用も可能である。これ等の
アルカリ性物質は直接固体のままで活性白土の水
溶液中に添加されても良いが、通常は稀薄なアル
カリ性溶液の状態にして分散水溶液中に添加され
処理される。 本発明による吸着剤のアルカリ性物質による処
理の程度は使用されるアルカリ性物質の種類およ
び活性白土の酸性成分の含有量によつて変わる
が、改質後の吸着剤の水中分散液の水素イオン濃
度(PH)は7.0以下にすることが好ましく、白土
臭だけを防止する場合は、PH7.0以上でも使用可
能であるが、食用油再生用膜として必要な吸着特
性を維持させるためPHは7.0以下が好ましい。 しかしアルカリ性物質による処理時におけるPH
は7.0以上でも、水洗および要すれば稀塩酸水に
よる中和操作によつてPHを7.0以下に低下させる
こともできる。しかし強アルカリ性で処理して吸
着剤の成分を大きく変化させることは避けるべき
であり、改質時のPHは7以下、好ましくは4〜6
である。 本発明において使用するパルプは天然および合
成繊維からなるもので耐熱性および食品衛生面で
安全なものであれば特に限定するものでないが、
高純度で強靭な植物性繊維、例えば綿、麻、レー
ヨン等が好ましい。繊維長および繊維直径は細く
て長く親水性のものが良い。本発明に用いられる
パルプは単独とは限らず2種以上の併用も可能で
ある。 本発明における再生用膜の組成はパルプ5〜95
重量部と吸着剤95〜5重量部の範囲で任意に選択
でき、パルプおよび吸着剤の種類によつて異なる
が、パルプ20〜40重量部と吸着剤80〜60重量部か
らなる組成のものが取扱いも易しくまた再生効率
が良く一層好ましい。 本発明の再生用膜はパルプと改質吸着剤の均一
混合層一層のみからなる膜とは限らず膜の層を多
層化構造とし、パルプと吸着剤の組成比を変えた
層を設けることも可能である。例えば上層はパル
プ単独にして中間層は吸着剤の量を多くして、下
層はパルプ層を多くした3層とする。又、同じ3
層でも上層と下層をパルプ量を多くして中間層を
吸着剤のみの層とする。或いは下層に薄い紙の層
を設け、その上にパルプと吸着剤からなる層を1
層または2層設ける等とすれば、輸送時および使
用時における膜中に含有される吸着剤の保護にも
役立つものである。 再生用膜の大きさは任意であるが、一般家庭用
としては100〜150m/mφの大きさのものが取扱
上からも好ましい。膜の厚さは面積が大になれば
再生効率と強度の点から厚くする必要があるが、
通常0.1〜5.0m/mの範囲の厚さである。 再生用膜の形状は、平板なシートに限定するも
のでなく、膜を器壁とする、天婦羅鍋から油が注
ぎ易い、口の大きなカツプ状に成形乃至整形した
ものでもよい。例えば再生用膜製造時に円錐形、
楕円形、角錐形等の錐形、若しくはこれら錐形に
ひだを付けたものなどの倒立した形状、前記各錐
形を截頭状にしたものを倒立したものに底を付し
たカツプ状その他任意の形状のカツプに成形する
こともでき、或いは平板状の膜2枚若しくはそれ
以上の側縁部を揃え、互の側縁部を柔軟性のある
無孔のテープによつて接合してカツプ状に整形す
ることもできる。特に2枚の扇形シートの両側お
よび底を接合したカツプは折畳み可能で且つ内部
に多量の油を入れて再生が行なえるので好まし
い。 本発明の再生用膜を用いて精製される食用油の
温度は吸着剤の特性と油の種類により多少異なる
が、食用油の場合その温度で分解変質しない限り
高温である方が再生効率の点で好ましく、一般に
80〜160℃の温度が最適である。通常天婦羅の揚
油の温度は180℃程度であるから、鍋から再生用
膜上に注ぐ時点において温度が低下し、この温度
範囲に入るので、揚げ物が終つた直後の高温の油
を直ちに膜上に注ぐのが好ましい。また調理後長
時間経つてから再生する場合も油の温度は60℃以
上に保つた方が油の粘度が下り過速度も速く、
また吸着精製もよく行なわれるので好ましい。 本発明を用いて食用油精製を行なう場合の再生
用膜の保持器はその形状によつては必ずしも必要
とするものではないが、例えば再生油の受器(保
存容器)の上部にカツプ状の保持器を設置し、こ
の中にカツプ状の再生用膜を固定した場合は、再
生油を他の容器に移す必要もなく取扱いが容易と
なる。又、保持器自体に加熱装置を設けたり、保
持器自体を摩法瓶に入れ保持する等により未再生
油の温度を一定温度以上に保ち吸着効率および
過速度等の向上を計ることが可能である。 本発明による再生用膜を用いて食用油の再生を
行なつた場合、白土臭は勿論ないが、更に膜の黒
化が少なく、再生熱油による膜からの気泡の発生
が少なく、過時間の短縮などの特徴を有するも
のである。 以下、実施例をもつて本発明を説明するが、実
施例に限定されるものでない。 実施例 1 10のビーカー内に活性白土(水沢化学製、粉
状)500g、浄水3を入れ100℃で5分間加熱攪
拌した。次に攪拌下にRT(室温)まで冷却した
上記活性白土水液に1/10規定炭酸水素ナトリウム
(NaHCO3)を100ml、200ml、400ml、600ml、
800ml入れ、各サンプルのPHを測定した。更に上
記物質の水分を除去するために、大判紙(東洋
紙製)を用い、過を行なつた後、乾燥器
(120℃)中で3時間乾燥させ水分を完全に除去し
た。 ミキサー(容量1.5)内に天然パルプ(東洋
紙製)10g、1/10規定炭酸水素ナトリウム
(NaHCO3)により処理された上記活性白土60
g、及び浄水1200gを投入し5分間混合した。次
にカツプ成形用多孔金型(上部径120mm〓、110mm
〓、高さ110mm、孔径1mm〓)を吸引槽に設置し
て多孔金型の外部を吸引ポンプを使い真空状態と
して上記の混合物を金型に吸引吸着させて脱水
し、倒立截頭円錐状のカツプを成形した。 更にウエツト状態のカツプ(多孔金型に吸着し
たまま)を乾燥器中で110℃で30分間乾燥し、水
分を除いた後、室温まで冷却して多孔金型から取
り出し、膜厚1.5mmの食用油用再生カツプを得た。 成形された再生カツプに天婦羅を揚げた油(天
婦羅油;野菜、魚、肉を各3回天婦羅したもの)
800gを160℃でカツプに注入して再生を行なつ
た。 原料油、再生用試料油(劣化油)および再生油
の光線透過率及び臭気を第1表に示す。 実施例 2 アルカリ性物質として1/10規定炭酸ナトリウム
(Na2CO3)を用い、油の過紙として天然パル
プ(東洋紙製)とレーヨンパルプ(東洋紡積
製)の混合紙を用いた他は実施例1と同じ揚げた
油の再生を行なつた。 再生結果は、第1表の通りである。 実施例 3 アルカリ性物質として1/10規定水酸化ナトリウ
ム(NaOH)を用いた他は実施例1と同じ揚げ
た油の再生を行なつた。 再生結果は第1表の通りである。 実施例 4 アルカリ性物質とし2/10規定水酸化カリウム
(KOH)を用いた他は実施例1と同じ揚げた油の
再生を行なつた。 再生結果は第1表の通りである。 実施例 5 アルカリ性物質として炭酸カリウム(K2CO3
を用いた他は、実施例1と同じ方法によつて揚げ
た油の再生を行なつた。 再生結果は第1表の通りである。 比較例 1 150℃まで冷却された実施例1と同じ天婦羅を
揚げた油800gに活性白土(水沢化学製、粉状)
60gを添加し撹拌器を用いて10分間混合した。 次にガラス製ロートにロ紙(東洋ロ紙大判)を
セツトして上記の混合物を過して再生油を得
た。 再生結果は第1表の通りである。 比較例 2 10のビーカー内に活性白土(水沢化学製粉
状)500g浄水3を入れ100℃で5分間加熱攪拌
した。 次に攪拌下にRT(室温)まで冷却した上記活
性白土(水液)をロ紙(東洋紙大判)で過を
行なつた後、乾燥器(120℃)中で3時間乾燥さ
せて水分を完全に除去した他は、実施例1と同じ
方法によつてカツプを成形し、実施例1と同じ天
婦羅を揚げた油の再生を行なつた。 再生結果は、第1表の通りである。
The present invention relates to a membrane for edible oil regeneration,
In particular, the present invention relates to an edible oil regeneration membrane for domestic use or small-scale commercial use, which adsorbs and passes impurities generated due to deterioration of frying oil, etc., and regenerates the frying oil. Edible oil used for deep-fried foods such as tempura and fries not only deteriorates due to chemical changes such as oxidation and polymerization, but also causes odors to be transferred from fried foods such as fish, meat, and vegetables. If used repeatedly, the taste of the prepared product will be impaired. Conventionally, commercially available household cooking oil regeneration equipment for regenerating fried oil containing degraded components as described above mainly removes solids mixed in fried oil, that is, used cooking oil, resulting in deterioration of the oil. However, there is a defect that various deterioration and deterioration components, fine particulate products, and odors mainly caused by thermal oxidation, thermal polymerization, thermal decomposition, and hydrolysis dissolved in oil are hardly removed. The fine particles themselves are overheated and decomposed, and the decomposed products affect the quality of the fried oil, such as coloring. As a result of various studies on the regeneration of fried oil, the present inventors have found that by applying a cup-shaped edible oil regeneration membrane mainly made of activated clay and pulp as an adsorbent, degraded components in fried oil can be removed. It was discovered that the oil could be substantially removed by adsorption and regenerated to a condition almost unchanged from that of the oil before use, and a patent application was filed in 1982.
No. 68495 and Japanese Patent Application No. 130462/1984. In these cases, as adsorbents, activated clay and acid clay have the best adsorption effect, and exhibit excellent adsorption properties in terms of decolorizing, deodorizing, defoaming, and smoke removal of deteriorated oil, but on the other hand, adsorption The slight odor of the agent itself, generally referred to as clay odor or clay odor, may transfer into fried foods and cooking oil, impairing the taste of tempura and other fries.Activated clay has a particularly sulfur odor. Purification methods using regeneration membranes were still unsatisfactory. As a result of further intensive research, the present inventors solved the above-mentioned problem by manufacturing a membrane for edible oil regeneration from pulp and a modified adsorbent obtained by treating the acidic components in activated clay with an alkaline substance. It has been discovered that it is not necessary to add any fine powder, and therefore, it is possible to refine edible oil without stirring, and that it is possible to obtain recycled oil that does not have a clay odor, which is also said to be the foul odor of activated clay. As is well known, edible oil has a high viscosity, and at room temperature the overspeed caused by a membrane material such as paper or cloth is extremely slow, but at high temperatures the viscosity decreases and the overspeed increases. On the other hand, adsorption and purification of oil is carried out more effectively at higher temperatures. The present inventors have proposed in Japanese Patent Application No. 55-68495 that the improvement in adsorption purification rate due to this temperature increase is more effective than the increase in overrate, so heated oil immediately after being used for cooking is used as an adsorbent. It was discovered that the adsorbent could be sufficiently purified by passing it once through a layer formed into a film, and it was found that it was most convenient to form the adsorbent into a film and use it as a material, and to form the film into a cup. I'm finding out. The present invention is characterized in that the adsorbent used in the regeneration membrane used in Japanese Patent Application No. 55-68495 is activated clay treated with an alkaline substance. It is intended to include not only the shape but also the original sheet shape. The present invention is a membrane for edible oil regeneration which includes one or more layers comprising 5 to 95 parts by weight of pulp and 95 to 5 parts by weight obtained by treatment with an alkaline substance. When degraded oil used for tempura is placed on top of this membrane, the oil permeates through the porous layer, and during this process, the degraded components and odor coloring in the oil are adsorbed. Solids such as fried crumbs and charred substances in the oil are also separated, and a refined oil without a clay odor is obtained as a liquid. The adsorbent used in the present invention is mainly a porous inorganic solid adsorbent obtained by treating the acidic component in activated clay with an alkaline substance, and may be used alone or in combination of two or more. The particle size of the granule and powder adsorbent is not particularly limited, but it is usually preferred to have a particle size of 500 μm or less. The alkaline substances used in the present invention are permitted for food hygiene and are safe even if contained in small amounts in the modifier, such as soda carbonate, sodium hydrogen carbonate, caustic soda, sodium pyrophosphate,
Slaked lime, quicklime, calcium oxide, calcium carbonate and other known inorganic alkaline substances,
They can be used alone or in combination of two or more. Although these alkaline substances may be added directly to the aqueous solution of activated clay as a solid, they are usually added to the dispersed aqueous solution in the form of a dilute alkaline solution for treatment. The degree of treatment of the adsorbent according to the present invention with an alkaline substance varies depending on the type of alkaline substance used and the content of acidic components in the activated clay, but the hydrogen ion concentration of the modified adsorbent dispersion in water ( PH) is preferably 7.0 or less, and if only clay odor is to be prevented, a PH of 7.0 or higher can be used, but in order to maintain the adsorption properties necessary as a membrane for edible oil regeneration, the PH should be 7.0 or less. preferable. However, the pH during treatment with alkaline substances
Even if the pH is 7.0 or higher, it can be lowered to 7.0 or lower by washing with water and, if necessary, neutralizing with diluted hydrochloric acid. However, it should be avoided to significantly change the adsorbent components by treatment with strong alkalinity, and the pH at the time of modification should be 7 or less, preferably 4 to 6.
It is. The pulp used in the present invention is not particularly limited as long as it is made of natural or synthetic fibers and is heat resistant and safe in terms of food hygiene.
High purity and tough vegetable fibers such as cotton, linen, rayon, etc. are preferred. The fiber length and fiber diameter are preferably long and thin and hydrophilic. The pulp used in the present invention is not limited to a single pulp, and two or more types can be used in combination. The composition of the regeneration membrane in the present invention is pulp 5-95
Parts by weight and adsorbent can be arbitrarily selected within the range of 95 to 5 parts by weight, depending on the type of pulp and adsorbent, but compositions consisting of 20 to 40 parts by weight of pulp and 80 to 60 parts by weight of adsorbent are It is more preferable because it is easy to handle and has good regeneration efficiency. The regeneration membrane of the present invention is not limited to a membrane consisting of only a single homogeneous mixed layer of pulp and modified adsorbent, but may also have a multilayered membrane structure, with layers having different composition ratios of pulp and adsorbent. It is possible. For example, the upper layer may consist of only pulp, the middle layer may contain a larger amount of adsorbent, and the lower layer may contain three layers of pulp. Also, the same 3
Among the layers, the upper and lower layers contain a large amount of pulp, and the middle layer contains only the adsorbent. Alternatively, a thin paper layer is provided as the bottom layer, and one layer of pulp and adsorbent is added on top of that.
Providing a layer or two layers will also help protect the adsorbent contained in the membrane during transportation and use. The size of the regeneration membrane is arbitrary, but for general household use, a membrane with a size of 100 to 150 m/mφ is preferable from the viewpoint of handling. The thickness of the membrane needs to be increased as the area increases from the viewpoint of regeneration efficiency and strength.
The thickness usually ranges from 0.1 to 5.0 m/m. The shape of the regenerating membrane is not limited to a flat sheet, but may be shaped into a cup with a large mouth that uses the membrane as a vessel wall and allows easy pouring of oil from a tempura pot. For example, when manufacturing membranes for recycling, conical shapes,
Conical shapes such as ellipses and pyramids, or inverted shapes such as pleated conical shapes, cup-shaped inverted truncated conical shapes with a bottom, and other arbitrary shapes. Alternatively, the side edges of two or more flat membranes may be aligned and joined with flexible non-porous tape to form a cup. It can also be formatted into In particular, a cup made by joining two fan-shaped sheets on both sides and at the bottom is preferable because it is foldable and can be recycled by putting a large amount of oil inside. The temperature of the edible oil refined using the regeneration membrane of the present invention varies somewhat depending on the characteristics of the adsorbent and the type of oil, but in the case of edible oil, as long as it does not decompose and deteriorate at that temperature, a higher temperature is better for regeneration efficiency. preferred and generally
A temperature of 80-160°C is optimal. Normally, the temperature of frying oil for tempura is around 180℃, so the temperature drops when it is poured from the pan onto the recycling membrane, and it falls within this temperature range. It is preferable to pour it on top. Also, when regenerating a long time after cooking, it is better to keep the oil temperature above 60℃, as this will reduce the viscosity of the oil and speed up the overspeed.
It is also preferred because adsorption purification is often carried out. When refining edible oil using the present invention, a holder for the regenerating membrane is not necessarily required depending on its shape, but for example, a cup-shaped holder may be placed on the top of the regenerated oil receiver (storage container). If a holder is installed and a cup-shaped regeneration membrane is fixed therein, there is no need to transfer the regenerated oil to another container, and handling becomes easy. In addition, it is possible to improve adsorption efficiency, overspeed, etc. by keeping the temperature of unregenerated oil above a certain temperature by installing a heating device in the retainer itself, or by placing the retainer itself in a vacuum bottle and holding it. be. When edible oil is recycled using the recycling membrane according to the present invention, there is of course no clay odor, but there is also less blackening of the membrane, less bubbles from the membrane caused by the recycled hot oil, and less overtime. It has characteristics such as shortening. The present invention will be explained below with reference to examples, but is not limited to the examples. Example 1 500 g of activated clay (manufactured by Mizusawa Chemical Co., Ltd., powder) and purified water 3 were placed in a 10-piece beaker and heated and stirred at 100° C. for 5 minutes. Next, 100 ml, 200 ml, 400 ml, 600 ml of 1/10N sodium bicarbonate (NaHCO 3 ) was added to the above activated clay aqueous solution cooled to RT (room temperature) while stirring.
800 ml was added to each sample and the pH of each sample was measured. Furthermore, in order to remove water from the above substance, it was filtered using large paper (manufactured by Toyo Paper Co., Ltd.), and then dried in a dryer (120°C) for 3 hours to completely remove water. In a mixer (capacity 1.5), 10 g of natural pulp (manufactured by Toyo Paper) and the above activated clay 60 treated with 1/10 normal sodium bicarbonate (NaHCO 3 ) were added.
g and 1200 g of purified water were added and mixed for 5 minutes. Next, a perforated mold for cup molding (upper diameter 120mm, 110mm)
〓, height 110 mm, pore diameter 1 mm〓) was installed in a suction tank, and the outside of the multi-hole mold was vacuumed using a suction pump, and the above mixture was suctioned into the mold and dehydrated, forming an inverted truncated conical shape. A cup was formed. Furthermore, the wet cup (still adsorbed to the porous mold) was dried in a dryer at 110°C for 30 minutes to remove moisture, cooled to room temperature, taken out from the porous mold, and made into an edible cup with a film thickness of 1.5 mm. A recycled cup for oil was obtained. Oil in which tempura is fried in a molded recycled cup (tempura oil; vegetables, fish, and meat are fried three times each)
Regeneration was carried out by pouring 800 g into a cup at 160°C. Table 1 shows the light transmittance and odor of the raw oil, sample oil for recycling (degraded oil), and recycled oil. Example 2 1/10 normal sodium carbonate (Na 2 CO 3 ) was used as the alkaline substance, and a mixed paper of natural pulp (manufactured by Toyo Paper Co., Ltd.) and rayon pulp (manufactured by Toyo Boseki Co., Ltd.) was used as the oil filtration paper. The same frying oil regeneration as in Example 1 was carried out. The reproduction results are shown in Table 1. Example 3 The same frying oil was regenerated as in Example 1 except that 1/10N sodium hydroxide (NaOH) was used as the alkaline substance. The reproduction results are shown in Table 1. Example 4 The same frying oil was regenerated as in Example 1 except that 2/10N potassium hydroxide (KOH) was used as the alkaline substance. The reproduction results are shown in Table 1. Example 5 Potassium carbonate (K 2 CO 3 ) as an alkaline substance
The frying oil was regenerated in the same manner as in Example 1, except that the same method as in Example 1 was used. The reproduction results are shown in Table 1. Comparative Example 1 Activated clay (manufactured by Mizusawa Chemical, powder) was added to 800 g of the same tempura frying oil as in Example 1 that had been cooled to 150°C.
60g was added and mixed for 10 minutes using a stirrer. Next, a glass funnel was set with roll paper (Toyo Roll Paper large size) and the above mixture was passed through it to obtain recycled oil. The reproduction results are shown in Table 1. Comparative Example 2 500g of activated clay (Mizusawa Chemical powder) was placed in a 10-piece beaker, and the mixture was heated and stirred at 100°C for 5 minutes. Next, the activated clay (aqueous liquid) cooled to RT (room temperature) with stirring was filtered through Ro paper (Toyo paper large format), and then dried in a dryer (120°C) for 3 hours to remove moisture. Except that the oil was completely removed, cups were formed using the same method as in Example 1, and the oil used for frying tempura was recycled in the same manner as in Example 1. The reproduction results are shown in Table 1.

【表】【table】

【表】 尚、表中の光線透過率は、日立製作所製自記分
光光度計を用い、10×10×30mm石英セル中に試料
及びブランク(蒸留水)を入れて測定した450m
μの波長の光線の透過率である。又本発明の実施
例、比較例における臭気は、人間の感覚は化学的
な測定(例えば、酸化とPOVとラジカルボニル
価に相関があると言われているが)よりも鋭敏で
あることが多く、特に臭には色々のものがあり、
官能検査は実用上の問題とまつたく同じ次元に立
つので厳重な味覚テストによつて味覚審査員20名
を選定し、恒温恒湿の官能検査室で3点識別試験
法(○△×方式)によつて油の臭(風味)の評価
を行なつたものである。 表中の○は原料油に近い臭で、×は白土臭が強
いものであり、△は白土臭が多少残つているもの
を示す。 他の特性として酸化値(AV)、過酸化物価値
(POV)、泡立ち等についても測定したが、本発
明のカツプを用いた場合、市販のオイルフイルタ
ーとは比較にならない良い結果を示した。 尚、本発明によつて再生した油により天婦羅を
揚げた場合、実施例1〜6何れも新油(原料油)
で揚げたものと臭、色、味等が同じ程度であつ
た。 実施例 6 アルカリ性物質として水酸化カルシウム(Ca
(OH)2)を用い活性白土を実施例1と同じ方法
で処理した。 尚、水酸化カルシウム(Ca(OH)2)は10の
ビーカー内に8の蒸留水を入れ30gの水酸化カ
ルシウムを室温で約10分撹拌した後の上澄を使用
したものである。 ミキサー(1.5)内に天然パルプ(東洋紙
製)10g、上記白土60g、浄水1200gを投入し5
分間混合した。次にシート成形用多孔金型(縦
300mm、横600mm、孔径1mm〓)を吸引槽に設置し
て多孔金型の底部を吸引ポンプを使い上記の混合
物を吸引吸着させて脱水し、シートを成型した。
更にウエツト状態のシート(多孔金型に吸着した
まま)を乾燥器(110℃)中で30分間放置し水分
を除いた後、室温まで冷却して多孔金型から取り
はずした。そのシートを150〓の形に切断し、フ
ランジを有する容器にシリコンゴムのパツキンを
用いて設置した他は実施例1と同じ揚げた油の再
生を行なつた。再生結果は第1表の通りである。
[Table] The light transmittance in the table is measured at 450 m using a self-recording spectrophotometer manufactured by Hitachi, Ltd., with the sample and blank (distilled water) placed in a 10 x 10 x 30 mm quartz cell.
It is the transmittance of light with a wavelength of μ. In addition, human senses are often more sensitive to the odors in Examples and Comparative Examples of the present invention than in chemical measurements (for example, it is said that there is a correlation between oxidation, POV, and radical carbonyl value). There are many different types of odors, especially
Since sensory testing is on the same level as practical issues, we selected 20 taste judges through rigorous taste tests, and conducted a three-point discrimination test method (○△x method) in a constant temperature and humidity sensory testing room. The odor (flavor) of oil was evaluated. In the table, ○ indicates an odor similar to that of raw oil, × indicates a strong clay odor, and △ indicates an odor with some residual clay odor. Other properties such as oxidation value (AV), peroxide value (POV), and foaming were also measured, and when the cup of the present invention was used, it showed better results than commercially available oil filters. In addition, when tempura was fried using oil recycled according to the present invention, in all of Examples 1 to 6, new oil (raw oil) was used.
The odor, color, taste, etc. were about the same as those fried. Example 6 Calcium hydroxide (Ca
(OH) 2 ) was used to treat activated clay in the same manner as in Example 1. Calcium hydroxide (Ca(OH) 2 ) was obtained by stirring 30 g of calcium hydroxide in 8 portions of distilled water in 10 beakers at room temperature for about 10 minutes, and then using the supernatant. Pour 10g of natural pulp (manufactured by Toyo Paper), 60g of the above white clay, and 1200g of purified water into a mixer (1.5).
Mixed for a minute. Next, a perforated mold for sheet molding (vertical
300 mm wide, 600 mm wide, and pore diameter 1 mm) was placed in a suction tank, and the bottom of the porous mold was sucked and adsorbed using a suction pump to dehydrate the above mixture, and a sheet was molded.
Furthermore, the wet sheet (still adsorbed to the porous mold) was left in a dryer (110°C) for 30 minutes to remove moisture, cooled to room temperature, and removed from the porous mold. The frying oil was recycled in the same manner as in Example 1, except that the sheet was cut into 150 mm pieces and placed in a container with a flange using a silicone rubber gasket. The reproduction results are shown in Table 1.

Claims (1)

【特許請求の範囲】 1 パルプ5〜95重量部とアルカリ性水溶液で処
理した水中分散液のPHが7.0以下である活性白土
95〜5重量部とからなる層を1層以上含む食用油
再生膜。 2 吸着剤の混合割合の異なるパルプ層が多層に
積層されたことを特徴とする特許請求の範囲第1
項記載の食用油再生用膜。 3 膜がカツプ状に成形若しくは整形されている
ことを特徴とする特許請求の範囲第1項記載の食
用油再生用膜。
[Scope of Claims] 1. Activated clay in which the pH of an aqueous dispersion treated with 5 to 95 parts by weight of pulp and an alkaline aqueous solution is 7.0 or less.
An edible oil regenerating membrane comprising one or more layers comprising 95 to 5 parts by weight. 2. Claim 1, characterized in that multiple pulp layers with different adsorbent mixing ratios are laminated.
Membrane for edible oil regeneration as described in section. 3. The edible oil regenerating membrane according to claim 1, wherein the membrane is formed or shaped into a cup shape.
JP3050481A 1980-05-23 1981-03-05 Film for regenerating edible oil Granted JPS57147436A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP3050481A JPS57147436A (en) 1981-03-05 1981-03-05 Film for regenerating edible oil
GB8115441A GB2080350A (en) 1980-05-23 1981-05-20 Oil regenerating membrane
DE19813120531 DE3120531A1 (en) 1980-05-23 1981-05-22 OIL REGENERATION MEMBRANE AND THEIR USE
FR8110276A FR2482867A1 (en) 1980-05-23 1981-05-22 MEMBRANE FOR THE REGENERATION OF OILS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3050481A JPS57147436A (en) 1981-03-05 1981-03-05 Film for regenerating edible oil

Publications (2)

Publication Number Publication Date
JPS57147436A JPS57147436A (en) 1982-09-11
JPH0122815B2 true JPH0122815B2 (en) 1989-04-27

Family

ID=12305640

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3050481A Granted JPS57147436A (en) 1980-05-23 1981-03-05 Film for regenerating edible oil

Country Status (1)

Country Link
JP (1) JPS57147436A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4593127B2 (en) * 2003-02-24 2010-12-08 ヤマトヨ産業株式会社 Edible oil filtration filter and method for producing the same
JP6857017B2 (en) * 2016-12-15 2021-04-14 日清オイリオグループ株式会社 Oil composition

Also Published As

Publication number Publication date
JPS57147436A (en) 1982-09-11

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