JP7582901B2 - Sheet and method for manufacturing the sheet - Google Patents
Sheet and method for manufacturing the sheet Download PDFInfo
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- JP7582901B2 JP7582901B2 JP2021071639A JP2021071639A JP7582901B2 JP 7582901 B2 JP7582901 B2 JP 7582901B2 JP 2021071639 A JP2021071639 A JP 2021071639A JP 2021071639 A JP2021071639 A JP 2021071639A JP 7582901 B2 JP7582901 B2 JP 7582901B2
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- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 238000000034 method Methods 0.000 title description 8
- 210000004027 cell Anatomy 0.000 claims description 57
- 241000196324 Embryophyta Species 0.000 claims description 45
- 150000004676 glycans Chemical class 0.000 claims description 11
- 229920001282 polysaccharide Polymers 0.000 claims description 11
- 239000005017 polysaccharide Substances 0.000 claims description 11
- 238000003825 pressing Methods 0.000 claims description 10
- 210000004748 cultured cell Anatomy 0.000 claims description 9
- 229920005610 lignin Polymers 0.000 claims description 9
- 229920003002 synthetic resin Polymers 0.000 claims description 4
- 239000000057 synthetic resin Substances 0.000 claims description 4
- 235000017166 Bambusa arundinacea Nutrition 0.000 claims description 3
- 235000017491 Bambusa tulda Nutrition 0.000 claims description 3
- 240000000797 Hibiscus cannabinus Species 0.000 claims description 3
- 235000015334 Phyllostachys viridis Nutrition 0.000 claims description 3
- 239000011425 bamboo Substances 0.000 claims description 3
- 244000082204 Phyllostachys viridis Species 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 208000008842 sick building syndrome Diseases 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 239000002994 raw material Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 210000002421 cell wall Anatomy 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 241001330002 Bambuseae Species 0.000 description 2
- 238000003811 acetone extraction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 150000002632 lipids Chemical class 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 1
- 229920002488 Hemicellulose Polymers 0.000 description 1
- 229920002000 Xyloglucan Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003809 water extraction Methods 0.000 description 1
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Description
本開示は、シート及びシートの製造方法に関する。 This disclosure relates to a sheet and a method for manufacturing the sheet.
従来の木質ボードは、バイオマス(主に木材)をチップ状又は粉状にし、樹脂や接着剤と混ぜて形成されていた。木質ボードは、軽くて強いので、家具や住宅内装等に広く使用されている。
しかし、従来の木質ボードでは、使用する接着剤から、ホルムアルデヒド等の揮発成分が放出されるため、シックハウス症候群の原因となる可能性があった。
他方、植物細胞の培養法が検討されている(例えば特許文献1参照)。
しかし、植物細胞の用途は限定されており、植物細胞の新規な用途開発が望まれていた。
Conventional wood boards are made by cutting biomass (mainly wood) into chips or powder and mixing it with resin and adhesive. Because wood boards are light and strong, they are widely used for furniture and home interiors.
However, the adhesives used in conventional wood boards release volatile components such as formaldehyde, which can potentially cause sick house syndrome.
Meanwhile, methods for culturing plant cells have been investigated (see, for example, Patent Document 1).
However, the uses of plant cells are limited, and the development of new uses for plant cells has been desired.
本開示は、上記実情に鑑みてなされたものであり、植物培養細胞を有効に利用し、シックハウス症候群の原因とならないシートを得ることを目的とする。本開示は、以下の形態として実現することが可能である。 This disclosure was made in consideration of the above-mentioned circumstances, and aims to obtain a sheet that effectively utilizes cultured plant cells and does not cause sick house syndrome. This disclosure can be realized in the following forms.
植物培養細胞を熱プレスして形成されたシート。 A sheet formed by heat pressing cultured plant cells.
本開示のシートによれば、植物細胞を有効に利用できる。しかも、このシートは、シックハウス症候群の原因とならない。 The sheet disclosed herein allows for the effective use of plant cells. Moreover, this sheet does not cause sick house syndrome.
ここで、本開示の望ましい例を示す。
シートは、合成樹脂を含まないことが好ましい。
シートは、多糖類を含むことが好ましい。
シートは、リグニンを含むことが好ましい。
シートの製造方法は、植物培養細胞を熱プレスすることが好ましい。
Here, a preferred example of the present disclosure is given.
The sheet preferably does not contain synthetic resin.
The sheet preferably comprises a polysaccharide.
The sheet preferably comprises lignin.
The sheet is preferably produced by heat pressing the cultured plant cells.
以下、本開示を詳しく説明する。なお、本明細書において、数値範囲について「~」を用いた記載では、特に断りがない限り、下限値及び上限値を含むものとする。例えば、「10~20」という記載では、下限値である「10」、上限値である「20」のいずれも含むものとする。すなわち、「10~20」は、「10以上20以下」と同じ意味である。 The present disclosure is described in detail below. In this specification, when a numerical range is described using "to" it is intended to include the lower limit and the upper limit unless otherwise specified. For example, the description "10 to 20" is intended to include both the lower limit "10" and the upper limit "20". In other words, "10 to 20" has the same meaning as "10 or more and 20 or less".
1.シート
本開示のシートは、植物培養細胞を熱プレスして形成されている。シートの厚み、形状は、特に限定されない。
(1)植物培養細胞
植物培養細胞は、特に限定されない。植物培養細胞としては、入手が容易等の観点から、タケ細胞、及びケナフ細胞からなる群より選ばれる1種以上が好適に用いられる。
(2)植物培養細胞以外の原料
植物培養細胞以外の原料を用いてもよい。シートは、植物培養細胞のみを原料とすることが望ましい。
また、植物培養細胞以外の原料として不適切なものは、例えば、有機溶剤、石油由来成分等である。これらの成分を入れると、シックハウス症候群の原因となる可能性がある。
(3)シートの構成成分
シートには、植物培養細胞に由来する構成成分が含まれている。構成成分としては、多糖類、タンパク質、リグニン(フェノール性成分の一例)が例示される。
多糖類としては、細胞壁多糖類が例示される。多糖類の例は、セルロース、キシログルカン等のヘミセルロース、ペクチンである。シートにおける、多糖類の含有量は、特に限定されない。多糖類の含有量は、シート全体100重量%に対して、シートの強度の観点から、20重量%以上80重量%以下が好ましく、30重量%以上70重量%以下がより好ましく、40重量%以上60重量%以下が更に好ましい。
シートにおける、リグニンの含有量は、特に限定されない。リグニンの含有量は、シート全体100質量%に対して、シートの強度の観点から、0.1重量%以上20重量%以下が好ましく、0.5重量%以上15重量%以下がより好ましく、1重量%以上10重量%以下が更に好ましい。
シートには、合成樹脂を含まないことが望ましい。
1. Sheet The sheet of the present disclosure is formed by heat pressing cultured plant cells. The thickness and shape of the sheet are not particularly limited.
(1) Cultured plant cells The cultured plant cells are not particularly limited. From the viewpoint of easy availability, etc., it is preferable to use one or more types of cultured plant cells selected from the group consisting of bamboo cells and kenaf cells.
(2) Raw materials other than cultured plant cells Raw materials other than cultured plant cells may be used. It is preferable that the sheet be made only from cultured plant cells.
In addition, other than the cultured plant cells, inappropriate raw materials include, for example, organic solvents, petroleum-derived components, etc. Adding these components may cause sick house syndrome.
(3) Components of the Sheet The sheet contains components derived from cultured plant cells. Examples of the components include polysaccharides, proteins, and lignin (an example of a phenolic component).
Examples of polysaccharides include cell wall polysaccharides. Examples of polysaccharides include cellulose, hemicellulose such as xyloglucan, and pectin. The content of polysaccharides in the sheet is not particularly limited. The content of polysaccharides is preferably 20% by weight or more and 80% by weight or less, more preferably 30% by weight or more and 70% by weight or less, and even more preferably 40% by weight or more and 60% by weight or less, based on 100% by weight of the entire sheet, from the viewpoint of sheet strength.
The lignin content in the sheet is not particularly limited. From the viewpoint of sheet strength, the lignin content is preferably 0.1% by weight or more and 20% by weight or less, more preferably 0.5% by weight or more and 15% by weight or less, and even more preferably 1% by weight or more and 10% by weight or less, based on 100% by mass of the entire sheet.
It is preferable that the sheet does not contain synthetic resin.
2.シートの製造方法
(1)熱プレスする工程
本開示のシートの製造方法は、植物培養細胞を熱プレスする工程を有する。熱プレスの条件は、特に限定されない。
熱プレスの温度は、特に限定されない。熱プレスの温度は、植物培養細胞を軟化させてシートに成形しやすい状態とし、かつシートの変色を抑制する観点から、100℃以上130℃以下が好ましく、110℃以上120℃以下がより好ましい。
熱プレスの圧力は、特に限定されない。熱プレスの圧力は、植物培養細胞を十分に潰してシートに成形する観点から、2MPa以上10MPa以下が好ましく、3MPa以上7MPa以下がより好ましい。なお、熱プレスの圧力に到達するまで、3時間以上8時間以下の時間をかけて、徐々に圧力を増加させることが好ましい。徐々に圧力を増加させることで、複数の植物培養細胞同士が十分に馴染んで接着し易くなる。
熱プレスの時間は、特に限定されない。熱プレスの時間は、植物培養細胞を十分に潰してシートに成形する観点から、所定の温度及び圧力になってから1時間以上72時間以下が好ましく、12時間以上36時間以下がより好ましい。
2. Sheet Manufacturing Method (1) Heat Pressing Step The sheet manufacturing method of the present disclosure includes a step of heat pressing the cultured plant cells. The conditions of the heat pressing are not particularly limited.
The temperature of the heat press is not particularly limited. From the viewpoint of softening the cultured plant cells to make them easily moldable into a sheet and suppressing discoloration of the sheet, the temperature of the heat press is preferably 100° C. or more and 130° C. or less, and more preferably 110° C. or more and 120° C. or less.
The pressure of the heat press is not particularly limited. From the viewpoint of sufficiently crushing the plant cultured cells to form them into a sheet, the pressure of the heat press is preferably 2 MPa to 10 MPa, more preferably 3 MPa to 7 MPa. It is preferable to gradually increase the pressure over a period of 3 hours to 8 hours until the pressure of the heat press is reached. By gradually increasing the pressure, the multiple plant cultured cells can be sufficiently blended with each other and easily adhered to each other.
The time for the heat press is not particularly limited. From the viewpoint of sufficiently crushing the cultured plant cells and forming them into a sheet, the time for the heat press is preferably from 1 hour to 72 hours, more preferably from 12 hours to 36 hours, after the predetermined temperature and pressure are reached.
(2)その他の工程(任意工程)
シートの製造方法では、その他の工程として、植物培養細胞を培養する工程を備えていてもよい。
シートの製造方法では、その他の工程として、植物培養細胞を含む培養液をろ過又は乾燥(好ましくは凍結乾燥)する工程を備えていてもよい。
(2) Other steps (optional steps)
The sheet manufacturing method may further include a step of culturing cultured plant cells as another step.
The sheet manufacturing method may further include a step of filtering or drying (preferably freeze-drying) the culture solution containing the cultured plant cells.
3.本開示のシートの効果
本開示のシートにおいて植物培養細胞のみを原料に用いれば、シートの構成成分は天然成分のみであり、有機溶剤や接着剤等の添加剤は含まれないことになる。この場合には、シックハウス症候群の原因となる有機溶剤もその他の石油由来成分も使用していないので、次世代のエコ材料として期待できる。
また、植物培養細胞の培養を環境負荷の少ない工程にすれば、次世代のエコ材料として価値が高い。
また、本開示のシートは、植物細胞を有効に利用できる。
3. Effects of the Sheet of the Present Disclosure If the sheet of the present disclosure uses only cultured plant cells as the raw material, the constituent components of the sheet will be only natural components, and will not contain additives such as organic solvents or adhesives. In this case, no organic solvents or other petroleum-derived components that cause sick house syndrome are used, making it a promising next-generation eco-material.
Furthermore, if the cultivation of plant cultured cells could be made into a process with less environmental impact, they would be highly valuable as next-generation eco-materials.
Furthermore, the sheet of the present disclosure allows for the effective use of plant cells.
4.本開示のシートの製造方法の効果
本開示の製造方法によれば、簡易な方法で、植物培養細胞を有効に利用し、シックハウス症候群の原因とならないシートを得ることができる。
4. Effects of the Manufacturing Method of the Sheet of the Present Disclosure According to the manufacturing method of the present disclosure, it is possible to obtain a sheet that effectively utilizes cultured plant cells in a simple manner and does not cause sick house syndrome.
以下、実施例により本開示を更に具体的に説明する。
1.実験方法
次のようにしてシートを形成した。
(1)植物細胞を培養した。植物細胞には、タケ細胞及びケナフ細胞を採用した。
(2)ろ過で植物培養細胞と培養液を分け、植物培養細胞のみを得た。
(3)金型(ステンレス枠)に、植物培養細胞を入れた。この際に、植物培養細胞を金型に入れやすくするために、植物培養細胞に水を加えて金型内に流し込んでもいい。
(4)植物培養細胞が入った金型を熱プレス機にセットし、温度を110℃~120℃に調整した。
(5)徐々に圧力をかけ、5MPaになった後、24時間にわたって熱プレスした。
(6)その後、温度、圧力が常温、常圧に戻ったことを確認して、金型からシート(プレート)を取り出した。
<熱プレス条件>
圧力:5MPa
温度:110~120℃程度
時間:5MPa、120℃になってから24時間
The present disclosure will now be described more specifically with reference to examples.
1. Experimental Method A sheet was formed as follows.
(1) Plant cells were cultured. Bamboo cells and kenaf cells were used as plant cells.
(2) The plant culture cells and the culture solution were separated by filtration to obtain only the plant culture cells.
(3) The plant culture cells were placed in a mold (stainless steel frame). At this time, in order to make it easier to place the plant culture cells in the mold, water may be added to the plant culture cells and then poured into the mold.
(4) The mold containing the plant culture cells was placed in a heat press and the temperature was adjusted to 110°C to 120°C.
(5) Pressure was gradually applied until it reached 5 MPa, after which it was hot pressed for 24 hours.
(6) After that, it was confirmed that the temperature and pressure had returned to normal, and the sheet (plate) was then removed from the mold.
<Heat press conditions>
Pressure: 5 MPa
Temperature: 110-120°C Time: 5MPa, 24 hours after reaching 120°C
2.成分の分析
成分を分析した。分析結果を表1に示す。ここでは、シートの原料たる植物培養細胞を分析している。シートは、植物培養細胞を熱プレスしたものであり、熱プレスによって、成分は変化しないため、シートにおける各成分の割合は、植物培養細胞の成分割合と同じである。
成分分析は、以下の要領で行った。
(1)細胞培養
細胞試料となる植物細胞を培養した。
(2)細胞試料をろ過、洗浄し、その後、凍結乾燥した。この操作によって、成分分析用に洗浄及び乾燥させた。
(3)成分分析
(3.1)重量測定1
成分分析を行う前の細胞試料の重量を測定した。この重量を「重量1」とする。
(3.2)熱水抽出
細胞試料を熱水抽出して、主にタンパク質、遊離の糖類、無機物の除去を行った。重量1を測定した細胞試料を熱水中に入れ、3時間、攪拌した。処理後、ろ過し、乾燥した。
(3.3)アセトン抽出
熱水処理後の細胞試料からアセトン抽出によって、主に脂質を除去した。具体的には、細胞試料をアセトン中に入れ、8時間、攪拌した。アセトンでの処理後、ろ過し、乾燥させた。
(4)重量測定2
熱水及びアセトンでの抽出処理をした後の細胞試料の重量を測定した。この重量を「重量2」とする。抽出後の細胞試料は、細胞壁成分のみになっている。
(5)硫酸法
硫酸法によりリグニン量を測定した。硫酸法は、細胞試料の細胞壁の多糖類を酸加水分解し、残ったリグニン量を測定する方法である。
(5.1)
細胞試料に72% 硫酸を加え、室温で1時間、攪拌した。
(5.2)
細胞試料に硫酸濃度が3%になるように水を加え、100℃で3時間、攪拌した。
(5.3)
ろ過して、残渣を105℃のオーブンで一晩乾燥後、細胞試料の重さを測った。この重量を「重量3」とする。
(6)成分量の導き方
・抽出成分量(wt%)=((重量1)―(重量2))÷(重量1)×100
抽出成分量は、タンパク質、遊離の糖類、脂質、その他成分量である。
・リグニン成分量(wt%)=(重量3)÷(重量1)×100
・多糖類(細胞壁中の多糖成分)(wt%)
=100-抽出成分量(wt%)-リグニン成分量(wt%)
2. Analysis of components The components were analyzed. The analysis results are shown in Table 1. Here, the plant cultured cells, the raw material of the sheet, were analyzed. The sheet is made by heat pressing the plant cultured cells, and the components do not change due to the heat pressing, so the ratio of each component in the sheet is the same as the component ratio of the plant cultured cells.
The component analysis was carried out as follows.
(1) Cell Culture Plant cells to serve as cell samples were cultured.
(2) The cell samples were filtered, washed, and then freeze-dried, which allowed them to be washed and dried for component analysis.
(3) Component analysis (3.1)
The weight of the cell sample was measured before component analysis. This weight was designated as "
(3.2) Hot water extraction The cell sample was extracted with hot water to remove mainly proteins, free sugars, and inorganic substances. The cell sample, the weight of which was measured, was placed in hot water and stirred for 3 hours. After processing, the cell sample was filtered and dried.
(3.3) Acetone Extraction Lipids were mainly removed from the cell sample after hot water treatment by acetone extraction. Specifically, the cell sample was placed in acetone and stirred for 8 hours. After treatment with acetone, the cell sample was filtered and dried.
(4) Weight measurement 2
The weight of the cell sample after extraction with hot water and acetone was measured. This weight was designated as "Weight 2." After extraction, the cell sample consisted only of cell wall components.
(5) Sulfuric acid method The amount of lignin was measured by the sulfuric acid method, which is a method in which polysaccharides in the cell walls of a cell sample are hydrolyzed with acid and the amount of remaining lignin is measured.
(5.1)
72% sulfuric acid was added to the cell sample and stirred at room temperature for 1 hour.
(5.2)
Water was added to the cell sample so that the sulfuric acid concentration became 3%, and the mixture was stirred at 100° C. for 3 hours.
(5.3)
After filtering and drying the residue overnight in an oven at 105° C., the cell sample was weighed. This weight was designated as “Weight 3.”
(6) How to calculate the amount of components Extracted component amount (wt%) = ((weight 1) - (weight 2)) ÷ (weight 1) x 100
The amounts of extracted components include proteins, free sugars, lipids, and other components.
Lignin component amount (wt%) = (weight 3) ÷ (weight 1) × 100
Polysaccharides (polysaccharide components in cell walls) (wt%)
= 100 - amount of extracted components (wt%) - amount of lignin components (wt%)
3.実施例の効果
実施例のシートは、植物培養細胞のみを原料に用いているので、シートの構成成分は天然成分のみであり、有機溶剤や接着剤等の添加剤は含まれない。よって、これらのシートは、シックハウス症候群の原因となる有機溶剤もその他の石油由来成分も使用していないので、次世代のエコ材料として期待できる。
また、実施例のシートは、植物培養細胞の新規な用途として期待できる。
3. Effects of the Examples The sheets of the Examples use only plant cultured cells as raw materials, so the constituent components of the sheets are only natural components, and do not contain additives such as organic solvents or adhesives. Therefore, these sheets do not use organic solvents or other petroleum-derived components that cause sick house syndrome, and are therefore expected to be next-generation eco-materials.
Furthermore, the sheets of the examples are expected to be a new application for cultured plant cells.
前述の例は単に説明を目的とするものでしかなく、本開示を限定するものと解釈されるものではない。本開示を典型的な実施形態の例を挙げて説明したが、本開示の記述及び図示において使用された文言は、限定的な文言ではなく説明的及び例示的なものであると理解される。ここで詳述したように、その形態において本開示の範囲又は本質から逸脱することなく、添付の特許請求の範囲内で変更が可能である。ここでは、本開示の詳述に特定の構造、材料及び実施例を参照したが、本開示をここにおける開示事項に限定することを意図するものではなく、むしろ、本開示は添付の特許請求の範囲内における、機能的に同等の構造、方法、使用の全てに及ぶものとする。 The foregoing examples are merely illustrative and are not to be construed as limiting the present disclosure. While the present disclosure has been described with reference to exemplary embodiments, the words used in describing and illustrating the present disclosure are understood to be descriptive and exemplary, rather than limiting. As detailed herein, changes may be made within the scope of the appended claims without departing from the scope or nature of the present disclosure in its form. Although the detailed description of the present disclosure has referred to specific structures, materials, and examples, it is not intended that the present disclosure be limited to those disclosed herein, but rather that the present disclosure extends to all functionally equivalent structures, methods, and uses within the scope of the appended claims.
本開示は上記で詳述した実施形態に限定されず、本開示の請求項に示した範囲で様々な変形又は変更が可能である。 This disclosure is not limited to the embodiments detailed above, and various modifications and variations are possible within the scope of the claims of this disclosure.
1 …シート 1 ... sheet
Claims (5)
前記植物培養細胞を熱プレスする、シートの製造方法。 A method for producing the sheet according to any one of claims 1 to 4, comprising the steps of:
The method for producing a sheet comprises heat-pressing the cultured plant cells.
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| JP2014124801A (en) | 2012-12-25 | 2014-07-07 | Mywood 2 Kk | Molded product of plant, and method for molding the product |
| US20170107411A1 (en) | 2014-01-08 | 2017-04-20 | Cambond Limited | Bio-adhesives |
| WO2018062343A1 (en) | 2016-09-30 | 2018-04-05 | 合同会社レビアスファーマ | Particles and method of manufacturing same |
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| JP2014124801A (en) | 2012-12-25 | 2014-07-07 | Mywood 2 Kk | Molded product of plant, and method for molding the product |
| US20170107411A1 (en) | 2014-01-08 | 2017-04-20 | Cambond Limited | Bio-adhesives |
| WO2018062343A1 (en) | 2016-09-30 | 2018-04-05 | 合同会社レビアスファーマ | Particles and method of manufacturing same |
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