JPS60133002A - Preparation of pectin - Google Patents
Preparation of pectinInfo
- Publication number
- JPS60133002A JPS60133002A JP58238916A JP23891683A JPS60133002A JP S60133002 A JPS60133002 A JP S60133002A JP 58238916 A JP58238916 A JP 58238916A JP 23891683 A JP23891683 A JP 23891683A JP S60133002 A JPS60133002 A JP S60133002A
- Authority
- JP
- Japan
- Prior art keywords
- pectin
- extract
- pressing
- concentration
- insoluble component
- 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.)
- Granted
Links
- 239000001814 pectin Substances 0.000 title claims abstract description 58
- 229920001277 pectin Polymers 0.000 title claims abstract description 58
- 235000010987 pectin Nutrition 0.000 title claims abstract description 58
- 238000003825 pressing Methods 0.000 claims abstract description 17
- 239000000284 extract Substances 0.000 claims description 18
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 239000001913 cellulose Substances 0.000 abstract description 7
- 229920002678 cellulose Polymers 0.000 abstract description 7
- 239000005909 Kieselgur Substances 0.000 abstract description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 6
- 235000005979 Citrus limon Nutrition 0.000 abstract description 4
- 244000131522 Citrus pyriformis Species 0.000 abstract description 4
- 240000007594 Oryza sativa Species 0.000 abstract description 4
- 235000007164 Oryza sativa Nutrition 0.000 abstract description 4
- 235000009566 rice Nutrition 0.000 abstract description 4
- 241000196324 Embryophyta Species 0.000 abstract description 3
- 239000010451 perlite Substances 0.000 abstract description 3
- 235000019362 perlite Nutrition 0.000 abstract description 3
- 244000089742 Citrus aurantifolia Species 0.000 abstract description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 abstract description 2
- 235000011941 Tilia x europaea Nutrition 0.000 abstract description 2
- 239000004571 lime Substances 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract description 2
- 235000011430 Malus pumila Nutrition 0.000 abstract 1
- 235000015103 Malus silvestris Nutrition 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 15
- 238000001914 filtration Methods 0.000 description 9
- 239000002994 raw material Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000018044 dehydration Effects 0.000 description 6
- 238000006297 dehydration reaction Methods 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000005119 centrifugation Methods 0.000 description 5
- 238000005352 clarification Methods 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000010298 pulverizing process Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 241001672694 Citrus reticulata Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 239000010903 husk Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- AEMOLEFTQBMNLQ-DTEWXJGMSA-N D-Galacturonic acid Natural products O[C@@H]1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-DTEWXJGMSA-N 0.000 description 2
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- IAJILQKETJEXLJ-RSJOWCBRSA-N aldehydo-D-galacturonic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-RSJOWCBRSA-N 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- AEMOLEFTQBMNLQ-UHFFFAOYSA-N beta-D-galactopyranuronic acid Natural products OC1OC(C(O)=O)C(O)C(O)C1O AEMOLEFTQBMNLQ-UHFFFAOYSA-N 0.000 description 2
- 235000011869 dried fruits Nutrition 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 238000006198 methoxylation reaction Methods 0.000 description 2
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 description 1
- SHZGCJCMOBCMKK-JFNONXLTSA-N L-rhamnopyranose Chemical compound C[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O SHZGCJCMOBCMKK-JFNONXLTSA-N 0.000 description 1
- PNNNRSAQSRJVSB-UHFFFAOYSA-N L-rhamnose Natural products CC(O)C(O)C(O)C(O)C=O PNNNRSAQSRJVSB-UHFFFAOYSA-N 0.000 description 1
- 244000141359 Malus pumila Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000021016 apples Nutrition 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000015205 orange juice Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000010178 pectin extract Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Jellies, Jams, And Syrups (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
Description
【発明の詳細な説明】 本発明はペクチンの製造方法に関する。[Detailed description of the invention] The present invention relates to a method for producing pectin.
ペクチンは、細胞間の充填並びに組織の支持に役立つ物
質として、植物界一般に広く分布しているコロイド状の
細胞壁多糖類であって、主としてD−ガラクツロン酸の
α−1,4結合より構成され、アラビノース、ガラクト
ース、ラムノース等の中性糖を種々の割合で含有してい
る。Pectin is a colloidal cell wall polysaccharide that is widely distributed throughout the plant kingdom as a substance that helps fill spaces between cells and support tissues, and is mainly composed of α-1,4 bonds of D-galacturonic acid. It contains various proportions of neutral sugars such as arabinose, galactose, and rhamnose.
特ニレモン、ライム、オレンジ、グレープフルーツ等の
柑橘類の果皮、リンゴ等には良質のペクチンが相当責合
まれ、欧米諸国ではこれらを原料として・ペクチンの製
造がなされている。ペクチン分子中のD−ガラクツロン
酸のカルボキシル基は部分的にメチルエステル化されて
おり、メトキシル化度50%以上のものはハイメトキシ
ル(HM)ペクチン、50%以下のものはロウメトキシ
ル(LM)ペクチシと分類される。これらはそれぞれゲ
ル化の機構やゲル化条件が異なっているが、ペクチンが
低pH系で安定なゲルを形成するという性質、並びに低
pH系で保護コロイド的な働きをするという性質を利用
して、ジャム、ママレード、ゼリー菓子、果汁飲料、ヨ
ーグルト等として食品業界で広く利用されている。In particular, the peels of citrus fruits such as lemons, limes, oranges, and grapefruits, as well as apples, contain a considerable amount of high-quality pectin, and in Western countries, pectin is manufactured using these as raw materials. The carboxyl group of D-galacturonic acid in pectin molecules is partially methyl esterified, and those with a methoxylation degree of 50% or more are high methoxyl (HM) pectin, and those with a methoxylation degree of less than 50% are low methoxyl (LM) pectin. It is classified as Each of these has different gelation mechanisms and gelation conditions, but pectin forms a stable gel in a low pH system and acts like a protective colloid in a low pH system. It is widely used in the food industry as jam, marmalade, jelly sweets, fruit juice drinks, yogurt, etc.
柑橘類果皮等よりペクチンを製造する一般的な方法は次
のとおりである。果、皮を冷水又は/及び温水で数回洗
浄し、果皮中の糖、有機酸、色素等の水溶性物質を除去
し、次いで塩°酸、硫酸等の無機酸でペクチンを加熱抽
出する。この抽出液を遠心分離、圧搾分離等により不溶
解分を分離し、分離液に珪藻土等の沢過助剤を添加し清
澄f過を行う。得られた沢過液を濃縮してメタノール、
インプロビルアルコール、アセトン等の水混和性有機溶
剤を加えるか、あるいはアルミニウム、銅、鉄等の金属
の塩を添加してペクチンを該金属塩として沈殿させ、脱
水回収する。金属塩法による場合は続いて酸性アルコー
ル等で沈殿を洗浄し、金属分を除去して可溶化させる必
要がある。いずれの場合でも、ペクチンの沈殿を乾燥、
粉砕して粉末ペクチンとする。A general method for producing pectin from citrus peel etc. is as follows. The fruit and peel are washed several times with cold and/or hot water to remove water-soluble substances such as sugar, organic acids, and pigments in the peel, and then pectin is extracted by heating with an inorganic acid such as hydrochloric acid or sulfuric acid. Undissolved components are separated from this extract by centrifugation, compression, etc., and a filtration aid such as diatomaceous earth is added to the separated solution for clarifying and filtration. The obtained filtrate was concentrated to methanol,
A water-miscible organic solvent such as Improvil alcohol or acetone is added, or a salt of a metal such as aluminum, copper, or iron is added to precipitate pectin as the metal salt, and the pectin is recovered by dehydration. When using the metal salt method, it is necessary to wash the precipitate with acidic alcohol or the like to remove metal components and solubilize them. In either case, dry the pectin precipitate;
Grind into powdered pectin.
このような一般的なペクチンの製造方法における最大の
問題点は、ペクチンの抽出濃度の低さである。乾燥した
ペクチン原料果皮中に含まれるペクチンの割合は原料の
種類、産地、収穫時期等により一定でないが、はぼ10
〜20%程度と言われており、抽出を行った場合、ペク
チン分よりも不溶解の残有部分の方が圧倒的に多い状況
にある。不溶解残有の分離方法として例えば遠心分離を
利用する場合は、分離された残有の固形分濃度が低いた
めに、抽出液の濃度を高くすればするほど分離液の収率
が低下する。The biggest problem with such general pectin production methods is the low extraction concentration of pectin. The proportion of pectin contained in the dried pectin raw material pericarp varies depending on the type of raw material, production area, harvest time, etc.
It is said to be about ~20%, and when extraction is performed, the undissolved residual portion is overwhelmingly larger than the pectin portion. For example, when centrifugation is used as a method for separating undissolved residuals, the concentration of the separated residual solids is low, so the higher the concentration of the extract, the lower the yield of the separated liquid.
例えば抽出液i度が1%の場合には該分離液の収率が7
5%程度であるのに対し、濃度が1.5%程度になると
分離液の収率は50%程度に低下し、かえって不利な結
果を招く。圧搾法により残有分離を行う場合には、不溶
解分が極めて軟質であるため、ずべりが生じて十分な圧
搾ができず、残有の固形分濃度も上がらず、スクリーン
の目詰まり等を起こしゃすい。For example, if the degree of extraction liquid is 1%, the yield of the separated liquid is 7.
While it is about 5%, when the concentration is about 1.5%, the yield of the separated liquid decreases to about 50%, which rather brings about disadvantageous results. When separating the residual solids by the squeezing method, the undissolved matter is extremely soft, so it slips and cannot be squeezed sufficiently, and the concentration of the residual solids does not increase, resulting in clogging of the screen, etc. It's easy to wake up.
かかる事情により従来行われているペクチンで
の製造方法によれば、ペクチンの濃度限界はせいぜい1
%であり、これより高い場合には不溶解残有分離の困難
さから、かえって効率が低下する。しかし低濃度の溶液
を扱うことは、例えばアルコール法でペクチンを回収す
る場合のように、莫大な量のアルコールを必要として経
済的でなく、その他の方法によっても製造時の動力費用
や生産性の面から好ましくない。Due to these circumstances, according to the conventional manufacturing method using pectin, the concentration limit of pectin is at most 1
%, and if it is higher than this, the efficiency will decrease due to the difficulty of separating undissolved residues. However, handling low-concentration solutions is not economical as it requires a huge amount of alcohol, as is the case when recovering pectin using the alcohol method, and other methods also reduce power costs and productivity during production. I don't like it from a certain point of view.
本発明の目的は、ペクチンの抽出濃度を上げることによ
り、効率よくペクチンを製造する方法を提供することで
あった。An object of the present invention was to provide a method for efficiently producing pectin by increasing the extraction concentration of pectin.
本発明は、ペクチン含有植物よりペクチンを抽出して得
られる抽出液又はこの抽出液から分離された不溶解分に
、圧搾助剤を不溶解分100重量部に対し20重量部以
上添加し、圧搾して不溶解分を分離することを特徴とす
る、ペクチンの製造方法である。In the present invention, a pressing aid is added to an extract obtained by extracting pectin from a pectin-containing plant or an insoluble component separated from this extract, and a pressing aid is added to the insoluble component in an amount of 20 parts by weight or more based on 100 parts by weight of the insoluble component. This is a method for producing pectin, which is characterized by separating insoluble matter.
本発明によれば、ペクチンの抽出液に圧搾助剤を添加し
混合することにより、不溶解分を硬質化して圧搾を容易
ならしめると共に、圧搾液の流路を確保し、スクリーン
の目詰まりを起こさずに効率よく液を回収することがで
きる。According to the present invention, by adding and mixing a pressing aid to the pectin extract, insoluble matter is hardened to make pressing easier, and a flow path for the pressing liquid is secured, thereby preventing clogging of the screen. The liquid can be efficiently collected without causing any problems.
圧搾助剤としては珪藻土、パーライト、セルロース等の
r過助剤又はオガ屑、モミ殻、ペクチンの不溶解残有の
水洗物等を使用できるが、不溶解残有を硬質化するとい
う意味ではセルロース、オガ屑、モミ殻等が特に有効で
あり、スクリーンの目詰まり防止の意味からは珪藻土、
パーライト等のf過助剤が特に有効である。したがって
その実際の使用に当っては、その系に適合するようにこ
れらを適宜混合して使用する・ことも有利である。As a pressing aid, it is possible to use diatomaceous earth, perlite, cellulose, or other additives such as sawdust, rice husks, and washed pectin with undissolved residue, but in the sense of hardening the undissolved residue, cellulose is used. , sawdust, rice husks, etc. are particularly effective, and diatomaceous earth,
F superaids such as perlite are particularly effective. Therefore, in actual use, it is advantageous to mix these as appropriate to suit the system.
圧搾助剤の添加量は、不溶解物の量すなわちペクチンの
濃度に比例して定めることが好ましく、該添加物の種類
やペクチン製造原料にもよるが、絶乾の不溶解分100
重量部に′対し一般に60〜200重量部が適当である
。添加量が多すぎる場合には液の回収率が低下して好ま
しくないし、逆に少なすぎる場合には十分な圧搾ができ
ない。該添加物の添加方法としては、普通は抽出に際し
て添加するが、抽出液に添加してもよバ、抽出液を遠心
分離等により分離した分離不溶分に該添加物を混合して
圧搾してもよい。圧搾装置としてはイ、ジブレス、ロー
ラーミル等の普通の装置が用いられる。The amount of the pressing aid added is preferably determined in proportion to the amount of insoluble matter, that is, the concentration of pectin, and it depends on the type of the additive and the raw material for pectin production, but the amount of insoluble matter on bone dry 100
Generally, 60 to 200 parts by weight are suitable. If the amount added is too large, the recovery rate of the liquid will decrease, which is undesirable, while if it is too small, sufficient squeezing will not be possible. The additive is usually added during extraction, but it may also be added to the extract, or the additive may be mixed with the insoluble matter separated from the extract by centrifugation, etc., and then squeezed. Good too. As a pressing device, a common device such as a jig press, a roller mill, etc. is used.
実施例1
夏みかん搾汁果皮の乾燥物1.5 kgを水洗したのち
水中に添加し、全体量を20kgとしたのち塩酸でpH
を20とし、90℃で60分間攪拌して抽出を行った。Example 1 1.5 kg of dried squeezed summer mandarin peel was washed with water, added to water to make a total amount of 20 kg, and then adjusted to pH with hydrochloric acid.
was set to 20, and the mixture was stirred at 90° C. for 60 minutes to perform extraction.
絶乾の不溶留分は約900gである。次いで抽出液に珪
藻土濾過助剤70g及びセルロース濾過助剤400gを
混合して圧搾し、不溶解残有3.3 kgと搾汁液17
.1kgを得た。搾汁液に珪藻土濾過助剤を0.5%添
加して清澄濾過を行い、得られたP液に60%濃度とな
るよフイソプロビルアルコールを加工、析出したペクチ
ンの沈殿を分離し、この沈殿を乾燥、粉砕して粉末ペク
チン220gを得た。製品ペクチンの原料果皮に対する
収率は147%であり、抽出液のペクチン濃度は140
%であった。The absolute dry insoluble fraction is approximately 900 g. Next, 70 g of diatomaceous earth filter aid and 400 g of cellulose filter aid were mixed with the extract and squeezed to obtain 3.3 kg of undissolved residue and 17 g of squeezed liquid.
.. 1 kg was obtained. Add 0.5% diatomaceous earth filter aid to the squeezed juice and perform clarification filtration, process the resulting P liquid with fisoprobil alcohol to a concentration of 60%, separate the precipitated pectin, and remove the precipitate. was dried and ground to obtain 220 g of powdered pectin. The yield of product pectin based on the raw material peel is 147%, and the pectin concentration of the extract is 140%.
%Met.
実施例2
レモンの搾汁果皮の乾燥物1.5kl?を実施例1と同
様にして水洗、抽出し、絶乾の不溶留分850gの抽出
液にセルロース系濾過助剤500gを添加し、圧搾し、
て不溶残有2.61\9と搾汁液17、9 kgを得た
。以下実施例1と同様にして清澄濾過し、脱水、乾燥、
粉砕を行って粉末ペクチン275Iを得た。製品ペクチ
ンの原料果皮に対する収率は183%であり、抽出液の
ペクチン濃度は1.75%であった。Example 2 1.5kl of dried lemon juice and peel? was washed with water and extracted in the same manner as in Example 1, and 500 g of cellulose filter aid was added to the bone-dry extract of 850 g of the insoluble fraction, and the mixture was squeezed.
2.61 kg of undissolved residue and 17.9 kg of squeezed liquid were obtained. Thereafter, clarifying filtration was carried out in the same manner as in Example 1, dehydration, drying,
Pulverization was performed to obtain powdered pectin 275I. The yield of product pectin based on the raw material pericarp was 183%, and the pectin concentration of the extract was 1.75%.
実施例6
夏みかん搾汁果皮の乾燥物21(gを実施例1と同様に
して水洗、抽出し、抽出液にセルロース濾過助剤200
I及びモミ殻800gを添加し、圧搾して不溶解残有3
.5 kgと搾汁液17.5kgを得た。以下実施例1
と同様にして清澄濾過し、脱水、乾燥、粉砕を行って粉
末ペクチン256gを得た。製品ペクチンの原料果皮に
対する収率は12.8%であり、ペクチン濃度は1.8
3%であった。Example 6 21 (g) of dried fruit of squeezed summer mandarin peel was washed with water and extracted in the same manner as in Example 1, and 200 g of cellulose filter aid was added to the extract.
Add I and 800g of rice husks and press to remove undissolved residue 3
.. 5 kg and 17.5 kg of squeezed liquid were obtained. Example 1 below
Clarification filtration was carried out in the same manner as above, followed by dehydration, drying and pulverization to obtain 256 g of powdered pectin. The yield of product pectin based on the raw material peel is 12.8%, and the pectin concentration is 1.8
It was 3%.
比較例1
夏みたん搾汁果皮の乾燥物1 kgを実施例1と同様に
して水洗、抽出し、抽出液を圧搾助剤を加えずに遠心分
離して、残有4.6 kgと分離液154kgを得た。Comparative Example 1 1 kg of dried fruit squeezed summer mitan fruit peel was washed with water and extracted in the same manner as in Example 1, and the extract was centrifuged without adding a pressing aid to separate the remaining 4.6 kg. 154 kg of liquid was obtained.
以下実施例1と同様にして清澄濾過し、脱水、乾燥、粉
砕を行って粉末ペクチン140gを得た。製品ペクチン
の原料果皮に対する収率は14.0%であり、抽出液の
濃度は0.96%であった。この場合は収率は良好であ
るが、抽出液が低濃度でペクチンの製造コストの点で好
ましくない。Thereafter, clarification filtration, dehydration, drying, and pulverization were performed in the same manner as in Example 1 to obtain 140 g of powdered pectin. The yield of product pectin based on the raw material pericarp was 14.0%, and the concentration of the extract was 0.96%. In this case, the yield is good, but the concentration of the extract is low, which is unfavorable in terms of the production cost of pectin.
比較例2
レモンの搾汁果皮の乾燥物1.5 klilを実施例1
と同様にして水洗、抽出し、抽出液を圧搾助剤を加えず
に圧搾して、不溶解残有1.4 kgと搾汁液18.6
kgを得た。搾汁液中に不溶留分が多く、清nL濾過が
困難なため、さらに遠心分離を行って残有7.4 k1
7と分離液11.2 kgを得た。以下実施例1と同様
にして清澄濾過し、脱水、乾燥、粉砕を行って粉末ペク
チン201gを得た。製品ペクチンの原料果皮に対する
収率は13.4%であり、ペクチン濃度は実施例2のそ
れと同じである。実施例2と比°較して収率が著しく低
下する。Comparative Example 2 1.5 kli of dried lemon juice and peel was added to Example 1.
Washed with water and extracted in the same manner as above, and the extract was pressed without adding any pressing aids to obtain 1.4 kg of undissolved residue and 18.6 kg of squeezed liquid.
I got kg. Since there was a large amount of insoluble fraction in the squeezed juice and it was difficult to filter the pure nL, further centrifugation was performed to reduce the remaining amount to 7.4 k1.
7 and 11.2 kg of separated liquid were obtained. Thereafter, clarification filtration, dehydration, drying, and pulverization were performed in the same manner as in Example 1 to obtain 201 g of powdered pectin. The yield of product pectin based on the raw material pericarp was 13.4%, and the pectin concentration was the same as that in Example 2. The yield is significantly lower than in Example 2.
比較例6
夏みかん搾汁果皮の乾燥物21(gを実施例1と同様に
して水洗、抽出し、絶乾の不溶留分1200Iの抽出液
にセルロース濾過助剤200g分が多く清澄濾過が困難
なため、さらに遠心分離を行って残有8.8 k!9と
分離液9.3 kgを得た。Comparative Example 6 21 (g) of dried summer mandarin orange juice peel was washed with water and extracted in the same manner as in Example 1, and the bone-dried extract of insoluble distillate 1200I contained a large amount of cellulose filter aid 200g, making clarifying filtration difficult. Therefore, further centrifugation was performed to obtain 8.8 k!9 remaining and 9.3 kg of separated liquid.
以下実施例1と同様にして清澄濾過し、脱水、乾燥、粉
砕を行って粉末ペクチン165gを得た。製品ペクチン
の原料果fに対する収率は8゜3%であり、ペクチン濃
度は実施例6のそれと同じである。実施例6と比較して
収率が著しく低下する。Thereafter, clarification filtration, dehydration, drying, and pulverization were performed in the same manner as in Example 1 to obtain 165 g of powdered pectin. The yield of product pectin based on raw fruit f was 8.3%, and the pectin concentration was the same as that in Example 6. The yield is significantly lower than in Example 6.
以上の実施例及び比較例から圧搾助剤の添加効果が明ら
かであり、好収率を維持しながらペクチン濃度を高める
ことが可能であることが知られる。From the above Examples and Comparative Examples, the effect of adding the pressing aid is clear, and it is known that it is possible to increase the pectin concentration while maintaining a good yield.
なおこれらの実験で圧搾に用いた装置は、ハンスフエツ
ター社製スクリュープレス、P−スベンヤル型で、スク
リューの圧縮比1:8のものである。The device used for compression in these experiments was a P-Svenjar type screw press manufactured by Hansfetter, with a screw compression ratio of 1:8.
出願人 三菱アセテート株式会社 代理人 弁理士 小 林 正 雄Applicant: Mitsubishi Acetate Co., Ltd. Agent: Patent Attorney Masao Kobayashi
Claims (1)
抽出液又はこの抽出液から分離された不溶解分に、圧搾
助剤を不溶解分100重量部に対し20重量部以上添加
し、圧搾して不溶解分を分離することを特徴とする、ペ
クチンの製造方法。 2、圧搾助剤の添加量が不溶解分100重量部に対し3
0〜200重量部であることを特徴とする特許請求の範
囲第1項に記載の方法。[Claims] 1. To the extract obtained by extracting pectin from a pectin-containing plant or to the insoluble matter separated from this extract, 20 parts by weight or more of a pressing aid is added per 100 parts by weight of the insoluble matter. A method for producing pectin, characterized by separating the insoluble matter by squeezing the pectin. 2. The amount of pressing aid added is 3 parts per 100 parts by weight of insoluble matter.
The method according to claim 1, characterized in that the amount is 0 to 200 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58238916A JPH0643445B2 (en) | 1983-12-20 | 1983-12-20 | Pectin manufacturing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58238916A JPH0643445B2 (en) | 1983-12-20 | 1983-12-20 | Pectin manufacturing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60133002A true JPS60133002A (en) | 1985-07-16 |
JPH0643445B2 JPH0643445B2 (en) | 1994-06-08 |
Family
ID=17037174
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58238916A Expired - Lifetime JPH0643445B2 (en) | 1983-12-20 | 1983-12-20 | Pectin manufacturing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0643445B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000043424A1 (en) * | 1999-01-19 | 2000-07-27 | Fuji Oil Co., Ltd. | Pectin, process for producing the same, acidic protein foods with the use of the same and process for the production thereof |
KR100370962B1 (en) * | 2000-07-10 | 2003-02-06 | 지성규 | Manufacturing meth od of Acetylated pectin for eliminating Endocrine Disrupter from the system |
-
1983
- 1983-12-20 JP JP58238916A patent/JPH0643445B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000043424A1 (en) * | 1999-01-19 | 2000-07-27 | Fuji Oil Co., Ltd. | Pectin, process for producing the same, acidic protein foods with the use of the same and process for the production thereof |
US6632469B1 (en) | 1999-01-19 | 2003-10-14 | Fuji Oil Co., Ltd. | Pectin, method for its production, acidic protein foods incorporating it and method for their production |
KR100370962B1 (en) * | 2000-07-10 | 2003-02-06 | 지성규 | Manufacturing meth od of Acetylated pectin for eliminating Endocrine Disrupter from the system |
Also Published As
Publication number | Publication date |
---|---|
JPH0643445B2 (en) | 1994-06-08 |
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