CN113386234A - Composite board, wood and manufacturing method thereof - Google Patents
Composite board, wood and manufacturing method thereof Download PDFInfo
- Publication number
- CN113386234A CN113386234A CN202110677883.XA CN202110677883A CN113386234A CN 113386234 A CN113386234 A CN 113386234A CN 202110677883 A CN202110677883 A CN 202110677883A CN 113386234 A CN113386234 A CN 113386234A
- Authority
- CN
- China
- Prior art keywords
- wood
- mixed solution
- mixture
- raw materials
- hot
- 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
- 239000002023 wood Substances 0.000 title claims abstract description 132
- 239000002131 composite material Substances 0.000 title claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 238000007731 hot pressing Methods 0.000 claims abstract description 45
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000011259 mixed solution Substances 0.000 claims abstract description 34
- 239000000243 solution Substances 0.000 claims abstract description 33
- 239000000203 mixture Substances 0.000 claims abstract description 32
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000002994 raw material Substances 0.000 claims abstract description 25
- 239000000661 sodium alginate Substances 0.000 claims abstract description 24
- 235000010413 sodium alginate Nutrition 0.000 claims abstract description 24
- 229940005550 sodium alginate Drugs 0.000 claims abstract description 24
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims abstract description 22
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000002156 mixing Methods 0.000 claims abstract description 18
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims abstract description 17
- ZBUXMZFLCYRTOB-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C.CNC(=O)C=C ZBUXMZFLCYRTOB-UHFFFAOYSA-N 0.000 claims abstract description 17
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000001914 filtration Methods 0.000 claims abstract description 8
- 238000003756 stirring Methods 0.000 claims abstract description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 13
- 229910021538 borax Inorganic materials 0.000 claims description 11
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical group [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 claims description 11
- 239000004328 sodium tetraborate Substances 0.000 claims description 11
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 7
- 238000002791 soaking Methods 0.000 claims description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 27
- 230000000052 comparative effect Effects 0.000 description 8
- 239000005457 ice water Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 229920005610 lignin Polymers 0.000 description 4
- 229920002401 polyacrylamide Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004566 building material Substances 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- -1 phenolic aldehyde Chemical class 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- CPLKPWIIMHFKIQ-UHFFFAOYSA-N [Na+].OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)[O-] Chemical compound [Na+].OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)[O-] CPLKPWIIMHFKIQ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N3/00—Manufacture of substantially flat articles, e.g. boards, from particles or fibres
- B27N3/02—Manufacture of substantially flat articles, e.g. boards, from particles or fibres from particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N3/00—Manufacture of substantially flat articles, e.g. boards, from particles or fibres
- B27N3/002—Manufacture of substantially flat articles, e.g. boards, from particles or fibres characterised by the type of binder
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N3/00—Manufacture of substantially flat articles, e.g. boards, from particles or fibres
- B27N3/08—Moulding or pressing
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/56—Acrylamide; Methacrylamide
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Wood Science & Technology (AREA)
- Forests & Forestry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
The invention discloses a composite board, wood and a manufacturing method thereof, and belongs to the technical field of wood processing. The wood is prepared by mixing the raw materials and then hot-pressing; the raw materials comprise 70-75% of wood chips, 6-8% of sodium alginate solution, 0.8-1.5% of borate, 0.1-0.3% of pyrogallic acid, 15-20% of acrylamide, 0.1-0.3% of N, N-dimethyl bisacrylamide and 2-3% of ammonium persulfate. The invention also provides a wood manufacturing method, which comprises the steps of S1, adding the wood chips into the sodium alginate solution, and mixing to obtain a first mixed solution; s2, adding borate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution; s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution to obtain a mixture; and S4, filtering and hot-pressing the mixture to obtain wood. The wood has certain strength and can be repaired by self.
Description
Technical Field
The invention relates to the technical field of wood processing, in particular to a composite board, wood and a manufacturing method thereof.
Background
In daily life, wood is widely used as a basic building material in daily life in all aspects of life. The wood is a natural nano composite material, and has the advantages of light weight, high strength and high yield. Although wood is a good building material, wood chips are easily produced during the processing of wood, and are construction wastes, which are difficult to produce, and costly to clean, although wood processing waste is currently prepared and recycled by binding wood chips with phenol resin. However, the composite wood board prepared by the phenolic resin is easy to volatilize formaldehyde and is harmful to human bodies. Therefore, it is necessary to develop a healthy polymer wood without undesirable gas volatilization.
The composite board is prepared by adding the waste residues of the wood chips generated in the wood processing process into phenolic aldehyde and performing high-temperature hot pressing on the mixture. And (4) after cutting, sticking the cut composite board with a plastic board, and then sealing edges with plastic to prepare the composite board. The phenolic aldehyde composite board prepared by the method has low comprehensive cost and is widely applied.
There are also methods for bonding wood chips by modifying the surface chemical bonds of the wood chips, such as by soaking the saw dust in NaOH to soften it to remove lignin, then performing surface carboxylation with TEMPO, carboxyl and Ca2+Can generate stronger complexation. Then adding CaCl2Bonding the carboxylated sawdust together, and finally carrying out hot pressing to form the polymer wood; or adding NaOH into natural wood to remove lignin in the wood, and then performing hot-pressing compaction under a high pressure condition to prepare the high-strength polymer wood.
Conventional phenolic bonded composite panels are made by bonding wood chips with phenolic resin. The composite board core thus contains a significant amount of formaldehyde and is wrapped by the face sheets, which seal the edges of the board. The formaldehyde volatilization speed in the wood board is greatly reduced, so that the composite board can release formaldehyde for a long time, and once the seal of the composite board is damaged, the formaldehyde releasing speed is increased. The composite board is not a healthy building material. In addition, in the process of processing the composite board, formaldehyde is used, which can cause certain harm to the health of workers processing the composite board.
How to avoid using formaldehyde to obtain wood with certain strength is a technical problem which needs to be solved urgently.
Disclosure of Invention
The invention aims to overcome the technical defects, provides a composite board, wood and a manufacturing method thereof, and solves the technical problem of how to obtain wood with certain strength while avoiding using formaldehyde in the prior art.
In order to achieve the technical purpose, the technical scheme of the invention provides wood which is prepared by mixing raw materials and then hot-pressing; the raw materials comprise, by mass, 70-75% of sawdust, 6-8% of sodium alginate solution, 0.8-1.5% of borate, 0.1-0.3% of pyrogallic acid, 15-20% of acrylamide, 0.1-0.3% of N, N-dimethyl bisacrylamide, 2-3% of ammonium persulfate and 100% of total.
Further, the mass concentration of the sodium alginate solution is 1-2%.
Further, the borate is sodium tetraborate.
The invention also provides a manufacturing method of the wood, which comprises the following steps:
s1, adding wood chips into the sodium alginate solution according to the mixture ratio of the raw materials, and mixing to obtain a first mixed solution;
s2, adding borate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution;
s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution to obtain a mixture;
and S4, filtering and hot-pressing the mixture to obtain the wood.
Further, before step S2, the method further includes pre-treating the wood chips, specifically, soaking the wood chips in a sodium hydroxide solution for 3-4 days.
Further, before step S4, the method further comprises refrigerating the mixture at-30 ℃ to 0 ℃.
Further, in step S4, the hot pressing includes pressurizing and then heating.
Further, in step S4, the hot pressing conditions are: the hot pressing temperature is 60-100 ℃, and the hot pressing strength is 30-50 MPa.
Further, in step S1, the first mixed solution is obtained by mixing for 15 to 20 min.
The invention also provides a composite board which comprises the wood or the wood prepared by the manufacturing method.
Compared with the prior art, the invention has the beneficial effects that: according to the wood provided by the invention, sodium alginate can generate hydrogen bond action with hydroxyl on wood chips to enable the wood chips to be better dispersed, acrylamide and N, N-dimethyl bisacrylamide generate polymerization reaction under the action of ammonium persulfate to generate polyacrylamide, pyrogallic acid is easy to oxidize in the air, and the pyrogallic acid is combined with a polyacrylamide chain segment to generate strong viscosity after being oxidized, so that the dispersed wood chips can be tightly adhered together, the polyacrylamide with higher crosslinking degree and the sodium alginate form a double-network structure to form a polymer wood framework to improve the strength of the wood, meanwhile, the pyrogallic acid or the oxidized pyrogallic acid can generate dynamic chemical bonds with borate, the chemical bonds can be released under the condition of more water and can be reformed under the condition of less water, so that water can be added for repairing when the wood has slight cracks, so that the raw materials are hot-pressed to obtain the wood which has certain strength and can be repaired by self, and the raw materials do not contain formaldehyde.
Although the inside polyacrylamide of the wood provided by the invention is decomposed when encountering open fire, the generated gas is CO2And NO2The smell generated during combustion is the smell generated during combustion of wood, and the gas generated during combustion of the phenolic composite board contains a large amount of toxic gas, so that the wood provided by the invention is safe and healthy.
Drawings
FIG. 1 is a microscopic image of wood produced in example 1 of the present invention.
FIG. 2 is a graph showing the results of tensile strengths of example 1 of the present invention and comparative example 1.
FIG. 3 is a photograph of wood produced in example 1 of the present invention and comparative example 2; wherein fig. 3a is a picture of wood of comparative example 2 and fig. 3b is a picture of wood of example 1.
FIG. 4 is a photograph of the burning of wood produced in example 1 of the present invention; where figure 4a is wood before burning, figure 4b is wood in burning, and figure 4c is the moment away from the open flame; figure 4d shows the wood after burning.
FIG. 5 is a graph showing the results of comparing the strength of the wood produced in example 1 of the present invention with that of the wood after restoration; wherein, fig. 5a is a picture of the wood prepared in example 1, and fig. 5b is a picture of the repaired wood.
Detailed Description
The specific embodiment provides wood which is prepared by mixing raw materials and then carrying out hot pressing; the raw materials comprise, by mass, 70-75% of sawdust, 6-8% of sodium alginate solution, 0.8-1.5% of borate, 0.1-0.3% of pyrogallic acid, 15-20% of acrylamide, 0.1-0.3% of N, N-dimethyl bisacrylamide, 2-3% of ammonium persulfate and 100% in total; further, the mass concentration of the sodium alginate solution is 1-2%; the borate is sodium tetraborate.
The specific embodiment also provides a wood manufacturing method, which comprises the following steps:
s0, wood chips are pretreated, and the wood chips are soaked in a sodium hydroxide solution for 3-4 days; the wood chips are composed of lignin and cellulose, the cellulose is a structural substance, and partial lignin can be removed by soaking the wood chips in a sodium hydroxide solution, so that the strength is improved;
s1, adding a sodium alginate solution with the mass concentration of 1-2% into the pretreated wood chips according to the mixture ratio of the raw materials, and mixing for 15-20min to obtain a first mixed solution;
s2, adding borate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution;
s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution, and reacting in an ice-water bath to obtain a mixture; refrigerating the mixture at-30 ℃ to 0 ℃; the reaction in the ice-water bath is to reduce the reaction temperature, the main body of the material is realized by thermally initiating acrylamide polymerization, and the ice-water bath or cold storage is used for preventing the reaction, so that the polymerization reaction is prevented from occurring in advance, and the strength and the performance of wood formed in the subsequent hot pressing are influenced.
S4, filtering and hot-pressing the mixture to obtain wood in a hot-pressing mode of firstly pressurizing and then heating; the hot pressing conditions are as follows: the hot pressing temperature is 60-100 ℃, and the hot pressing strength is 30-50 MPa.
The reaction formula of pyrogallic acid (PG), sodium tetraborate (Borate) is as follows:
the specific embodiment also comprises a composite board which comprises the wood or the wood prepared by the manufacturing method.
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is described in further detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.
Example 1
This example presents a wood, made by mixing the raw materials, followed by hot pressing; the raw materials comprise, by mass, 70% of sawdust, 6.6% of sodium alginate solution, 0.94% of sodium tetraborate, 0.19% of pyrogallic acid, 19.63% of acrylamide, 0.19% of N, N-dimethyl bisacrylamide, 2.45% of ammonium persulfate and 100% of total; further, the mass concentration of the sodium alginate solution is 1%.
The embodiment further provides a manufacturing method of the wood, which includes the following steps:
s0, wood chips are pretreated, and the wood chips are soaked in a sodium hydroxide solution for 3 days;
s1, adding a sodium alginate solution with the mass concentration of 1% into the pretreated wood chips according to the mixture ratio of the raw materials, and mixing for 15min to obtain a first mixed solution;
s2, adding sodium tetraborate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution;
s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution, and reacting in an ice-water bath to obtain a mixture; refrigerating the mixture at-18 ℃;
s4, filtering and hot-pressing the mixture to obtain wood in a mode of pressurizing and then heating; the hot pressing conditions are as follows: the hot pressing temperature is 80 ℃, and the hot pressing strength is 30 MPa. As can be seen from fig. 1, the wood chips are clearly seen to be bonded together in the wood produced in this example. It should be noted that FIG. 1 was obtained by a polarizing microscope model C40P, which is available from Ningbo Shunhu instruments Ltd.
Example 2
This example presents a wood, made by mixing the raw materials, followed by hot pressing; the raw materials comprise 73% of sawdust, 7.2% of sodium alginate solution, 1.2% of sodium tetraborate, 0.3% of pyrogallic acid, 15% of acrylamide, 0.3% of N, N-dimethyl bisacrylamide and 3% of ammonium persulfate, wherein the total amount is 100%; further, the mass concentration of the sodium alginate solution is 1.5%.
The embodiment further provides a manufacturing method of the wood, which includes the following steps:
s0, wood chips are pretreated, and the wood chips are soaked in a sodium hydroxide solution for 4 days;
s1, adding a sodium alginate solution with the mass concentration of 1.5% into the pretreated wood chips according to the mixture ratio of the raw materials, and mixing for 20min to obtain a first mixed solution;
s2, adding sodium tetraborate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution;
s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution, and reacting in an ice-water bath to obtain a mixture; refrigerating the mixture at-30 ℃;
s4, filtering and hot-pressing the mixture to obtain wood in a mode of pressurizing and then heating; the hot pressing conditions are as follows: the hot pressing temperature is 60 ℃, and the hot pressing strength is 50 MPa.
Example 3
This example presents a wood, made by mixing the raw materials, followed by hot pressing; the raw materials comprise, by mass, 75% of sawdust, 6% of sodium alginate solution, 1% of sodium tetraborate, 0.2% of pyrogallic acid, 15% of acrylamide, 0.3% of N, N-dimethyl bisacrylamide, 2.5% of ammonium persulfate and 100% of total; further, the mass concentration of the sodium alginate solution is 2%.
The embodiment further provides a manufacturing method of the wood, which includes the following steps:
s0, wood chips are pretreated, and the wood chips are soaked in a sodium hydroxide solution for 4 days;
s1, adding a sodium alginate solution with the mass concentration of 2% into the pretreated wood chips according to the mixture ratio of the raw materials, and mixing for 18min to obtain a first mixed solution;
s2, adding sodium tetraborate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution;
s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution, and reacting in an ice-water bath to obtain a mixture; refrigerating the mixture at-5 ℃;
s4, filtering and hot-pressing the mixture, and pressurizing and then heating to obtain wood; the hot pressing conditions are as follows: the hot pressing temperature is 1000 ℃, and the hot pressing strength is 40 MPa.
Example 4
This example presents a wood, made by mixing the raw materials, followed by hot pressing; the raw materials comprise, by mass, 70% of sawdust, 8% of sodium alginate solution, 1.5% of sodium tetraborate, 0.1% of pyrogallic acid, 17.1% of acrylamide, 0.3% of N, N-dimethyl bisacrylamide and 3% of ammonium persulfate, wherein the total amount is 100%; further, the mass concentration of the sodium alginate solution is 2%.
The embodiment further provides a manufacturing method of the wood, which includes the following steps:
s0, wood chips are pretreated, and the wood chips are soaked in a sodium hydroxide solution for 4 days;
s1, adding a sodium alginate solution with the mass concentration of 1% into the pretreated wood chips according to the mixture ratio of the raw materials, and mixing for 15min to obtain a first mixed solution;
s2, adding sodium tetraborate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution;
s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution, and reacting in an ice-water bath to obtain a mixture; refrigerating the mixture at 0 ℃;
s4, filtering and hot-pressing the mixture, and pressurizing and then heating to obtain wood; the hot pressing conditions are as follows: the hot pressing temperature is 90 ℃, and the hot pressing strength is 45 MPa.
Comparative example 1
The wood produced by this comparative example differs from example 1 in that the wood chips have not been pretreated, i.e. have not been soaked in a sodium hydroxide solution.
From FIG. 2, it is possible to obtain a tensile strength of 6.14MPa for the wood without pretreatment, and a tensile strength of 11.03MPa for the wood with pretreatment.
Comparative example 2
The wood of this comparative example is different from example 1 in that after step S3, the mixture was filtered and put into a hot-pressed mold and dried in a drying oven at 80 ℃.
As can be seen from fig. 3, comparative example 2 has no rough surface of the wood obtained by hot pressing and is relatively loose; the surface of the compressed wood is smooth and compact.
Burning test
The wood prepared in example 1 is subjected to burning treatment on open fire, the wood before burning is complete and flat as can be seen from fig. 4a, the wood is extinguished after leaving a fire source as can be seen from fig. 4b to 4d, and black smoke is generated when the wood is not burned to produce open fire, which indicates that the wood is not easy to ignite.
Repair test
The method of example 1 was used to produce block wood, which was further cut into 8 pieces, after which 8 small pieces of wood were placed back into the mold again and dried in an oven with water at 80 ℃, after drying, water was added again and dried again, and the procedure was repeated five times to produce repaired wood. As can be seen from FIG. 5, the wood obtained in example 1 was compressed to a compression ratio of 0.72 at which it collapsed and had a compressive strength of 9.07MPa, while the repaired wood was compressed to a compression ratio of 0.61 at which it collapsed and had a compressive strength of 4.23 MPa. Therefore, the repaired wood also has better strength. And it can be seen from a comparison of fig. 5a and 5b that the shape of the repaired wood is substantially restored.
The above-described embodiments of the present invention should not be construed as limiting the scope of the present invention. Any other corresponding changes and modifications made according to the technical idea of the present invention should be included in the protection scope of the claims of the present invention.
Claims (10)
1. The wood is characterized in that the wood is prepared by mixing raw materials and then hot-pressing; the raw materials comprise, by mass, 70-75% of sawdust, 6-8% of sodium alginate solution, 0.8-1.5% of borate, 0.1-0.3% of pyrogallic acid, 15-20% of acrylamide, 0.1-0.3% of N, N-dimethyl bisacrylamide, 2-3% of ammonium persulfate and 100% of total.
2. The wood as claimed in claim 1, wherein the sodium alginate solution has a mass concentration of 1-2%.
3. Wood according to claim 1, characterized in that the borate is sodium tetraborate.
4. A method of making wood according to any one of claims 1 to 3, comprising the steps of:
s1, adding wood chips into the sodium alginate solution according to the mixture ratio of the raw materials, and mixing to obtain a first mixed solution;
s2, adding borate and pyrogallic acid into the first mixed solution, and continuously stirring to obtain a second mixed solution;
s3, adding acrylamide, N, N-dimethyl bisacrylamide and ammonium persulfate into the second mixed solution to obtain a mixture;
and S4, filtering and hot-pressing the mixture to obtain the wood.
5. The method of claim 4, further comprising pre-treating the wood chips, specifically soaking the wood chips in sodium hydroxide solution for 3-4 days, before the step S2.
6. The method of claim 4, further comprising refrigerating the mixture at-30 ℃ to 0 ℃ prior to step S4.
7. The method of claim 4, wherein said hot pressing comprises pressurizing and then heating in step S4.
8. The production method according to claim 7, wherein in step S4, the conditions of the hot pressing are: the hot pressing temperature is 60-100 ℃, and the hot pressing strength is 30-50 MPa.
9. The method of claim 4, wherein the first mixed solution is obtained by mixing for 15 to 20min in step S1.
10. A composite panel comprising wood according to any one of claims 1 to 3 or wood produced by the method of manufacture according to any one of claims 4 to 9.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110677883.XA CN113386234B (en) | 2021-06-18 | 2021-06-18 | Composite board, wood and manufacturing method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110677883.XA CN113386234B (en) | 2021-06-18 | 2021-06-18 | Composite board, wood and manufacturing method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113386234A true CN113386234A (en) | 2021-09-14 |
CN113386234B CN113386234B (en) | 2022-11-01 |
Family
ID=77621916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110677883.XA Expired - Fee Related CN113386234B (en) | 2021-06-18 | 2021-06-18 | Composite board, wood and manufacturing method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113386234B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116214655A (en) * | 2023-03-06 | 2023-06-06 | 南京林业大学 | Wood-based hydrogel and preparation method thereof |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2908793B1 (en) * | 1998-07-02 | 1999-06-21 | 善成 長谷川 | Board material manufacturing method |
CN101319058A (en) * | 2008-07-18 | 2008-12-10 | 东南大学 | Method for producing wood-plastic composite material and produced wood-plastic composite material |
JP2010158850A (en) * | 2009-01-09 | 2010-07-22 | Daiken Corp | Method of manufacturing wood fiber board |
CN102702538A (en) * | 2012-06-11 | 2012-10-03 | 东北林业大学 | Preparation method for wood flour mixing with hydrogel |
CN103396562A (en) * | 2013-07-09 | 2013-11-20 | 西安交通大学 | Preparation method for sodium alginate-acrylamide-based hydrogel |
CN110183927A (en) * | 2019-06-24 | 2019-08-30 | 四川轻化工大学 | A kind of preparation method and application of fire-proof heat-insulating material |
CN110587749A (en) * | 2019-09-20 | 2019-12-20 | 中国林业科学研究院木材工业研究所 | Complexing wood shavings, complexing shaving board and manufacturing method thereof |
CN110776667A (en) * | 2019-11-11 | 2020-02-11 | 浙江农林大学 | Piezoresistive sensing device material and preparation method and application thereof |
CN110981494A (en) * | 2019-12-18 | 2020-04-10 | 中国建筑材料科学研究总院有限公司 | Silicon carbide ceramic thick bulletproof plate and preparation method and application thereof |
CN112300336A (en) * | 2020-10-16 | 2021-02-02 | 江汉大学 | Self-repairable conductive hydrogel material and preparation method thereof |
CN112316219A (en) * | 2020-09-29 | 2021-02-05 | 浙江大学 | Anti-adhesion hydrogel-silk scaffold composite membrane and preparation and application thereof |
-
2021
- 2021-06-18 CN CN202110677883.XA patent/CN113386234B/en not_active Expired - Fee Related
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2908793B1 (en) * | 1998-07-02 | 1999-06-21 | 善成 長谷川 | Board material manufacturing method |
CN101319058A (en) * | 2008-07-18 | 2008-12-10 | 东南大学 | Method for producing wood-plastic composite material and produced wood-plastic composite material |
JP2010158850A (en) * | 2009-01-09 | 2010-07-22 | Daiken Corp | Method of manufacturing wood fiber board |
CN102702538A (en) * | 2012-06-11 | 2012-10-03 | 东北林业大学 | Preparation method for wood flour mixing with hydrogel |
CN103396562A (en) * | 2013-07-09 | 2013-11-20 | 西安交通大学 | Preparation method for sodium alginate-acrylamide-based hydrogel |
CN110183927A (en) * | 2019-06-24 | 2019-08-30 | 四川轻化工大学 | A kind of preparation method and application of fire-proof heat-insulating material |
CN110587749A (en) * | 2019-09-20 | 2019-12-20 | 中国林业科学研究院木材工业研究所 | Complexing wood shavings, complexing shaving board and manufacturing method thereof |
CN110776667A (en) * | 2019-11-11 | 2020-02-11 | 浙江农林大学 | Piezoresistive sensing device material and preparation method and application thereof |
CN110981494A (en) * | 2019-12-18 | 2020-04-10 | 中国建筑材料科学研究总院有限公司 | Silicon carbide ceramic thick bulletproof plate and preparation method and application thereof |
CN112316219A (en) * | 2020-09-29 | 2021-02-05 | 浙江大学 | Anti-adhesion hydrogel-silk scaffold composite membrane and preparation and application thereof |
CN112300336A (en) * | 2020-10-16 | 2021-02-02 | 江汉大学 | Self-repairable conductive hydrogel material and preparation method thereof |
Non-Patent Citations (1)
Title |
---|
乔海燕: "多功能水凝胶的制备及其在应变传感器中的应用", 《中国优秀博硕士学位论文全文数据库(硕士)工程科技Ⅰ辑》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116214655A (en) * | 2023-03-06 | 2023-06-06 | 南京林业大学 | Wood-based hydrogel and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN113386234B (en) | 2022-11-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN113386234B (en) | Composite board, wood and manufacturing method thereof | |
CN112321861B (en) | Cellulose phosphate nanofiber/black phosphorus quantum dot composite flame-retardant film and preparation method thereof | |
CN113878683B (en) | All-wood-based photothermal conversion film with high mechanical strength, light transmission and water resistance and preparation method thereof | |
CN111217560A (en) | Asbestos-free straw fiber reinforced cement board and preparation method thereof | |
CN115091572A (en) | Preparation method of environment-friendly high-strength flame-retardant decorative veneer | |
CN104760101A (en) | Production method of flame-retardant modified wood | |
CN112898625A (en) | Underwater elastic cellulose aerogel and preparation method and application thereof | |
CN102351466A (en) | Waterproof fireproof zero-carbon ecological sheet material manufactured from waste electric circuit board powder | |
KR102206991B1 (en) | bio composite wood using eco-friendly material and manufacturing method | |
CN110142844B (en) | Preparation method of glue-free fiber board | |
CN110670392A (en) | Processing technology for producing refractory plate by modified kraft paper | |
CN101579878A (en) | Manufacturing technique of self-bonding bamboo board | |
JP2005060590A (en) | Adhesive, woody composite material, method for producing woody composite material, and method for peeling adhesive | |
CN113736426A (en) | Method for simply and conveniently preparing carboxymethyl cellulose reinforced and toughened soybean protein adhesive | |
CN115891303B (en) | Flame-retardant honeycomb panel with waste textile as raw material and preparation method thereof | |
CN114621548B (en) | Polyvinylpyrrolidone-secondary collagen fiber composite material and preparation method and application thereof | |
CN115635555B (en) | Preparation method of environment-friendly high-strength wood composite material | |
CN116574452B (en) | Waterproof magnesium oxychloride inorganic adhesive for plywood and preparation method thereof | |
CN117025002B (en) | Fireproof flame-retardant composite board and preparation method thereof | |
CN118006251A (en) | Pullulan/mussel mucin compounded low-toxicity boron-free adhesive for bonding wooden relics | |
LU102640B1 (en) | A straw recombination integration material and its preparation method | |
US20240185823A1 (en) | Method for producing a sound absorbing panel | |
CN116285010A (en) | Preparation method of cellulose/seaweed polysaccharide flame-retardant composite material | |
CN117645443A (en) | High-carbon-fixation fiber cement board and preparation method thereof | |
CN111116046A (en) | Preparation method of high-strength flame-retardant waterproof glass wool |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20221101 |