EP3951049A1 - High-performance environment-friendly kraft liner board, and preparation method thereof - Google Patents
High-performance environment-friendly kraft liner board, and preparation method thereof Download PDFInfo
- Publication number
- EP3951049A1 EP3951049A1 EP21166623.5A EP21166623A EP3951049A1 EP 3951049 A1 EP3951049 A1 EP 3951049A1 EP 21166623 A EP21166623 A EP 21166623A EP 3951049 A1 EP3951049 A1 EP 3951049A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pulp
- kraft liner
- liner board
- short fiber
- styrene
- 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
- 239000002655 kraft paper Substances 0.000 title claims abstract description 46
- 238000002360 preparation method Methods 0.000 title claims description 22
- 239000000835 fiber Substances 0.000 claims abstract description 134
- 239000010410 layer Substances 0.000 claims abstract description 72
- 239000003063 flame retardant Substances 0.000 claims abstract description 68
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 65
- 239000004816 latex Substances 0.000 claims abstract description 50
- 229920000126 latex Polymers 0.000 claims abstract description 50
- 229920001909 styrene-acrylic polymer Polymers 0.000 claims abstract description 47
- 239000002023 wood Substances 0.000 claims abstract description 38
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000002131 composite material Substances 0.000 claims abstract description 30
- 238000000576 coating method Methods 0.000 claims abstract description 19
- 239000011248 coating agent Substances 0.000 claims abstract description 15
- 239000011247 coating layer Substances 0.000 claims abstract description 15
- 238000004537 pulping Methods 0.000 claims abstract description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 60
- 238000003756 stirring Methods 0.000 claims description 41
- 238000006243 chemical reaction Methods 0.000 claims description 36
- 238000002156 mixing Methods 0.000 claims description 31
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 22
- AQNSVANSEBPSMK-UHFFFAOYSA-N dicyclopentenyl methacrylate Chemical compound C12CC=CC2C2CC(OC(=O)C(=C)C)C1C2.C12C=CCC2C2CC(OC(=O)C(=C)C)C1C2 AQNSVANSEBPSMK-UHFFFAOYSA-N 0.000 claims description 22
- 238000010438 heat treatment Methods 0.000 claims description 21
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 19
- 238000012216 screening Methods 0.000 claims description 19
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 18
- 239000000843 powder Substances 0.000 claims description 18
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 18
- 239000003513 alkali Substances 0.000 claims description 14
- 238000004513 sizing Methods 0.000 claims description 14
- 238000007865 diluting Methods 0.000 claims description 13
- 206010042674 Swelling Diseases 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 230000008961 swelling Effects 0.000 claims description 12
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 11
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 11
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 11
- 238000007761 roller coating Methods 0.000 claims description 11
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical compound O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 claims description 11
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 10
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 claims description 10
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 10
- 238000001914 filtration Methods 0.000 claims description 10
- 238000010030 laminating Methods 0.000 claims description 10
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 10
- 229940051841 polyoxyethylene ether Drugs 0.000 claims description 10
- 229920000056 polyoxyethylene ether Polymers 0.000 claims description 10
- 238000003825 pressing Methods 0.000 claims description 10
- 238000007670 refining Methods 0.000 claims description 10
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 claims description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 9
- 230000014759 maintenance of location Effects 0.000 claims description 9
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 9
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 9
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 9
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 claims description 9
- 238000012545 processing Methods 0.000 claims description 8
- 230000009172 bursting Effects 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 238000010521 absorption reaction Methods 0.000 claims description 5
- 238000013459 approach Methods 0.000 claims description 5
- 238000003490 calendering Methods 0.000 claims description 5
- 239000003999 initiator Substances 0.000 claims description 5
- 230000007935 neutral effect Effects 0.000 claims description 5
- 239000002562 thickening agent Substances 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- 239000004114 Ammonium polyphosphate Substances 0.000 claims description 4
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims description 4
- 229920001276 ammonium polyphosphate Polymers 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229920000877 Melamine resin Polymers 0.000 claims description 3
- 229920000388 Polyphosphate Polymers 0.000 claims description 3
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 3
- 239000001205 polyphosphate Substances 0.000 claims description 3
- 235000011176 polyphosphates Nutrition 0.000 claims description 3
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 claims description 2
- 238000002715 modification method Methods 0.000 claims description 2
- -1 polyphosphoester Polymers 0.000 claims description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims 1
- 230000007613 environmental effect Effects 0.000 abstract description 2
- 239000000123 paper Substances 0.000 description 16
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 14
- 238000005516 engineering process Methods 0.000 description 9
- 238000010009 beating Methods 0.000 description 8
- 125000002091 cationic group Chemical group 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 229920002401 polyacrylamide Polymers 0.000 description 8
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 8
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 7
- 239000003607 modifier Substances 0.000 description 7
- 239000002994 raw material Substances 0.000 description 6
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- 235000011114 ammonium hydroxide Nutrition 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 239000010893 paper waste Substances 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 230000007547 defect Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000012744 reinforcing agent Substances 0.000 description 2
- 239000002352 surface water Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H11/00—Pulp or paper, comprising cellulose or lignocellulose fibres of natural origin only
- D21H11/14—Secondary fibres
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21B—FIBROUS RAW MATERIALS OR THEIR MECHANICAL TREATMENT
- D21B1/00—Fibrous raw materials or their mechanical treatment
- D21B1/04—Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres
- D21B1/12—Fibrous raw materials or their mechanical treatment by dividing raw materials into small particles, e.g. fibres by wet methods, by the use of steam
- D21B1/30—Defibrating by other means
- D21B1/34—Kneading or mixing; Pulpers
- D21B1/345—Pulpers
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21D—TREATMENT OF THE MATERIALS BEFORE PASSING TO THE PAPER-MAKING MACHINE
- D21D1/00—Methods of beating or refining; Beaters of the Hollander type
- D21D1/20—Methods of refining
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21D—TREATMENT OF THE MATERIALS BEFORE PASSING TO THE PAPER-MAKING MACHINE
- D21D5/00—Purification of the pulp suspension by mechanical means; Apparatus therefor
- D21D5/02—Straining or screening the pulp
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21F—PAPER-MAKING MACHINES; METHODS OF PRODUCING PAPER THEREON
- D21F11/00—Processes for making continuous lengths of paper, or of cardboard, or of wet web for fibre board production, on paper-making machines
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/06—Paper forming aids
- D21H21/10—Retention agents or drainage improvers
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/34—Ignifugeants
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
- D21H23/22—Addition to the formed paper
- D21H23/52—Addition to the formed paper by contacting paper with a device carrying the material
- D21H23/56—Rolls
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/10—Packing paper
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/30—Multi-ply
Definitions
- the present invention relates to the manufacturing and processing technical field of carton boards, in particular to a high-performance environment-friendly kraft liner board, and a preparation method thereof.
- Carton boards are the most important raw materials for wrapping cartons. With the improvement of people's living standards and social progress, many high-grade cartons for commodity wrapping need to consume a large number of high-performance carton boards. With the continuous development of China's paper industry, the shortage of fiber raw materials has become a bottleneck issue that restricts sustainable development of the paper industry. Thus, waste paper which is widely applied in carton boards manufacturing enterprises also limits the improvement of product performance.
- kraft liner boards for various wrapping cartons are generally made of waste paper, and without utilizing flame retardant treatment in most cases.
- some high-grade wrapping cartons or special products such as export products, a small number of high-grade consumer products, flammable and explosive products, military products, require flame retardant wrapping and transportation in particular.
- electric commercial cartons whether they are ordinary cartons or cartons for wrapping color TVs, refrigerators and other high-grade electrical appliances, the kraft liner boards used among them are generally without flame retardant treatment, it is a hidden danger, fires happen occasionally during transportation or storage of wrapping cartons.
- With the development of society and the improvement of people's living requirements it is an inevitable requirement to treat kraft liner boards with flame retardants for wrapping cartons.
- some wrapping carton products adopt the method of adding plenty of flame retardants in the pulp to get the flame retardant performance, but the added amount is large, the effect is limited, the cost is high, and the physical strength of the products is affected.
- kraft liner boards are used to wrap higher-grade products, so they have higher requirements on their quality performance, especially in the process of box making, such as stretching and folding, which requires good folding endurance, tensile strength, and ring crush compression strength. After being made into cartons, good bursting strength and water resistance are required during wrapping and transportation. In order to improve the wrapping effect, the surface requiresaji printing, so kraft liner boards also require good surface smoothing performance.
- the prior art mainly adopts surface sizing method to improve the ring crush compression strength and surface water resistance of products, which has many defects: surface sizing can mainly improve the surface strength and partial ring crush compression resistance of the products, but have limited effect on improving the overall physical strength of the products, such as tensile strength, bursting strength and folding endurance, so the physical properties of the kraft liner boards mainly produced by waste paper are restricted. Therefore, a large number of reinforcing agents require to be added in the production process to solve the problems, and the loss is large and the cost is high. Moreover, the usage of surface sizing has a certain effect on improving the surface water resistance and lowering the Cobb value of the product, but it has limited effect on improving the overall water resistance of the kraft liner boards. Furthermore, the usage of surface sizing can improve the surface smoothness of the products to a certain extent, but it is difficult to achieve the effect of high-quality wrapping and printing products.
- objects of the present invention are to provide a high-performance environment-friendly kraft liner board, and a preparation method thereof.
- the present invention adopts technical solutions as follows.
- a high-performance environment-friendly kraft liner board comprising a bottom layer, a top layer and a coating layer, which are arranged successively in an order from bottom to top; wherein: the bottom layer is made of a bottom layer pulp composed of a modified wood powdery pulp and a short fiber pulp; the top layer is made of a top layer pulp composed of a long fiber pulp and a short fiber pulp; the coating layer is formed through coating a flame retardant styrene-acrylic latex on the top layer; the long fiber pulp and the short fiber pulp are formed through pulping old domestic corrugated boxes; the flame retardant styrene-acrylic latex consists of modified composite flame retardants, a functional modified styrene-acrylic latex and water.
- a basis weight of the high-performance environment-friendly kraft liner board is100-120 g/m 2
- a ring pressure index is 6.7-7.6 mN ⁇ m 2 /g
- a frontal water absorption is 30-31 g/m 2
- a limit oxygen index is 30-33%
- a smoothness is 15-16 seconds
- a bursting index is 2.4-2.6 kPa ⁇ m 2 /g
- a folding endurance is 15-20 times.
- a weight percentage concentration of the flame retardant styrene-acrylic latex is 2.0-5.0%.
- a weight ratio of the modified composite flame retardants to the functional modified styrene-acrylic latex is 1:2.5-3.0.
- the modified composite flame retardants are prepared through modifying composite flame retardants with a modifier; wherein: the modifier is a silane coupling agent; more preferably, the silane coupling agent is N-( ⁇ -aminoethyl)-r-aminopropyltrimethoxysilane.
- a weight ratio of the modifier to the composite flame retardants is (0.002-0.01): 1.
- the composite flame retardants contain two or more flame retardant elements.
- the composite flame retardants may be a combination of any two or more of ammonium polyphosphate, polyphosphoester, melamine polyphosphate, zinc borate, aluminum phosphate, aluminum hydroxide, etc., and a ratio of each flame retardant element is not specifically limited.
- the composite flame retardants consist of two or more flame retardant elements of equal weight.
- the zinc borate are ultra-fine powders with a particle size of 0.02-0.04 um.
- the aluminum hydroxide are ultra-fine powders with a particle size of 0.03-0.05 um.
- a preparation method of the modified composite flame retardants is as follows: mixing the composite flame retardants with the modifier, and stirring evenly.
- the functional modified styrene-acrylic latex is prepared through steps of:
- a weight ratio of the dicyclopentenyl methacrylate, the water, the sodium dodecyl sulfate, the nonylphenol polyoxyethylene ether, the trimethylene carbonate, the acrylic acid, the hydroxyethyl acrylate, the butyl acrylate, the styrene, the sodium bicarbonate and the initiator is 1:40-50:0.2-0.3:0.3-0.4:1-1.3:0.2-0.5:4-6: 25-35:25-35:0.2-0.4:0.4-0.6.
- the initiator is a persulfate salt, and specifically can be any one of ammonium persulfate, sodium persulfate or potassium persulfate.
- a pH regulator adopts ammonia water.
- the dicyclopentenyl methacrylate is prepared through steps of:
- an agitator speed is 100-500 r/min.
- a weight ratio of the methacrylic acid, the trifluoromethanesulfonic acid, the hydroquinone, the dicyclopentadiene and the NaOH is 0.8-1.2:0.002-0.004:0.00006-0.0001:1.5-2.0:0.0015-0.002.
- a weight percentage concentration of the long fiber pulp is 3.5-4.5%
- a weight percentage concentration of the short fiber pulp is 4-5%
- a weight percentage concentration of the modified wood powdery pulp is 3-5%.
- a weight ratio of the modified wood powdery pulp to the short fiber pulp is 5-10:95-90.
- the modified wood powdery pulp is prepared through modifying wood powders with a swelling agent, and the swelling agent is a mixed alkali; a modification method is as follows: after processing the wood powders with a refiner, successively adding the mixed alkali and water, stirring evenly, then heating an obtained mixture to 70-90°C, and a swelling treatment is carried out at constant temperature for 60-90 minutes to form the modified wood powdery pulp.
- the water used for the swelling agent modifying wood powders adopts dryer condensed water in a double-stacked paper machine, which is used for preparing products of the present invention.
- a weight ratio of the long fiber pulp to the short fiber pulp is 80-90:20-10.
- a weight ratio of the top layer pulp to the bottom layer pulp is 40-50:60-50.
- a ratio of total weight of absolute dry fibers contained in the bottom layer pulp and the top layer pulp to a weight of the coating layer is 1:0.005-0.015.
- a second object of the present invention is to provide a preparation method for the above high-performance environment-friendly kraft liner board, comprising steps of:
- a first-stage pressure screen of the fine screening for first level three stages adopts a micro-slot width pressure screen to remove binders, and a screen slot width is 0.08-0.12 mm.
- a weight ratio of absolute dry long fibers in the long fiber coarse pulp obtained by screen sizing to absolute dry short fibers in the short fiber coarse pulp is 30-40:70-60.
- the long fiber pulp adopts conical refiners in series to refine the pulp, and adopts a long fiber viscous beating technology, and a beating degree is 28-30 °SR.
- a weight percentage concentration of the long fiber pulp is 3.5-4.5%, and a weight percentage concentration of the short fiber pulp is 4-5%.
- the water in the step (i) and step (ii) both adopts dryer condensed water in a double-stacked paper machine.
- the retention and drainage aids in the step (2) consist of two components: cationic polyacrylamide and silica sol, wherein: a weight ratio of absolute dry fibers, cationic polyacrylamide, and silica sol is 1:0.001-0.002:0.001-0.002; the absolute dry fibers refer to total amounts of absolute dry fibers contained in the bottom layer pulp and the top layer pulp.
- the coating in the step (2) adopts the metering roller coating technology, specifically, by a metering roller coating method, coating the flame retardant styrene-acrylic latex on the top layer of the kraft liner board obtained through double-folding, laminating, pressing and drying, so as to form a coating layer.
- FIG. 1 is a preparation process flow chart of the high-performance environment-friendly kraft liner board according to the present invention.
- the method for preparing a high-performance environment - friendly kraft liner board comprising following steps of:
- the preparation method of a high-performance environment - friendly kraft liner board comprising following steps of:
- the preparation method of a high-performance environment - friendly kraft liner board comprising following steps of: (1) prepareing for a flame retardant styrene-acrylic latex
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Abstract
Description
- The application claims priority to Chinese patent application No.
202010587201.1, filed on June 24, 2020 - The present invention relates to the manufacturing and processing technical field of carton boards, in particular to a high-performance environment-friendly kraft liner board, and a preparation method thereof.
- Carton boards are the most important raw materials for wrapping cartons. With the improvement of people's living standards and social progress, many high-grade cartons for commodity wrapping need to consume a large number of high-performance carton boards. With the continuous development of China's paper industry, the shortage of fiber raw materials has become a bottleneck issue that restricts sustainable development of the paper industry. Thus, waste paper which is widely applied in carton boards manufacturing enterprises also limits the improvement of product performance.
- The technical problems need to be solved by the present invention are described as follow:
- Currently, kraft liner boards for various wrapping cartons are generally made of waste paper, and without utilizing flame retardant treatment in most cases. However, some high-grade wrapping cartons or special products, such as export products, a small number of high-grade consumer products, flammable and explosive products, military products, require flame retardant wrapping and transportation in particular. Moreover, electric commercial cartons, whether they are ordinary cartons or cartons for wrapping color TVs, refrigerators and other high-grade electrical appliances, the kraft liner boards used among them are generally without flame retardant treatment, it is a hidden danger, fires happen occasionally during transportation or storage of wrapping cartons. With the development of society and the improvement of people's living requirements, it is an inevitable requirement to treat kraft liner boards with flame retardants for wrapping cartons. In the prior art, some wrapping carton products adopt the method of adding plenty of flame retardants in the pulp to get the flame retardant performance, but the added amount is large, the effect is limited, the cost is high, and the physical strength of the products is affected.
- Solving the surface performance, water resistance and strength problems of high-performance carton boards.
- Conventionally, kraft liner boards are used to wrap higher-grade products, so they have higher requirements on their quality performance, especially in the process of box making, such as stretching and folding, which requires good folding endurance, tensile strength, and ring crush compression strength. After being made into cartons, good bursting strength and water resistance are required during wrapping and transportation. In order to improve the wrapping effect, the surface requires exquisite printing, so kraft liner boards also require good surface smoothing performance. The prior art mainly adopts surface sizing method to improve the ring crush compression strength and surface water resistance of products, which has many defects: surface sizing can mainly improve the surface strength and partial ring crush compression resistance of the products, but have limited effect on improving the overall physical strength of the products, such as tensile strength, bursting strength and folding endurance, so the physical properties of the kraft liner boards mainly produced by waste paper are restricted. Therefore, a large number of reinforcing agents require to be added in the production process to solve the problems, and the loss is large and the cost is high. Moreover, the usage of surface sizing has a certain effect on improving the surface water resistance and lowering the Cobb value of the product, but it has limited effect on improving the overall water resistance of the kraft liner boards. Furthermore, the usage of surface sizing can improve the surface smoothness of the products to a certain extent, but it is difficult to achieve the effect of high-quality wrapping and printing products.
- Based on above reasons, the present invention is provided.
- Aiming at above problems or defects in the prior art, objects of the present invention are to provide a high-performance environment-friendly kraft liner board, and a preparation method thereof.
- In order to accomplish the first object, the present invention adopts technical solutions as follows.
- A high-performance environment-friendly kraft liner board, comprising a bottom layer, a top layer and a coating layer, which are arranged successively in an order from bottom to top; wherein: the bottom layer is made of a bottom layer pulp composed of a modified wood powdery pulp and a short fiber pulp; the top layer is made of a top layer pulp composed of a long fiber pulp and a short fiber pulp; the coating layer is formed through coating a flame retardant styrene-acrylic latex on the top layer; the long fiber pulp and the short fiber pulp are formed through pulping old domestic corrugated boxes; the flame retardant styrene-acrylic latex consists of modified composite flame retardants, a functional modified styrene-acrylic latex and water.
- Further, in the above technical solution, a basis weight of the high-performance environment-friendly kraft liner board is100-120 g/m2, a ring pressure index is 6.7-7.6 mN·m2/g, a frontal water absorption is 30-31 g/m2, and a limit oxygen index is 30-33%, a smoothness is 15-16 seconds, a bursting index is 2.4-2.6 kPa·m2/g, and a folding endurance is 15-20 times.
- Further, in the above technical solution, a weight percentage concentration of the flame retardant styrene-acrylic latex is 2.0-5.0%.
- Further, in the above technical solution, a weight ratio of the modified composite flame retardants to the functional modified styrene-acrylic latex is 1:2.5-3.0.
- Further, in the above technical solution, the modified composite flame retardants are prepared through modifying composite flame retardants with a modifier; wherein: the modifier is a silane coupling agent; more preferably, the silane coupling agent is N-(β-aminoethyl)-r-aminopropyltrimethoxysilane.
- Further, in the above technical solution, a weight ratio of the modifier to the composite flame retardants is (0.002-0.01): 1.
- Further, in the above technical solution, the composite flame retardants contain two or more flame retardant elements. For example, the composite flame retardants may be a combination of any two or more of ammonium polyphosphate, polyphosphoester, melamine polyphosphate, zinc borate, aluminum phosphate, aluminum hydroxide, etc., and a ratio of each flame retardant element is not specifically limited.
- Preferably, in the above technical solution, the composite flame retardants consist of two or more flame retardant elements of equal weight.
- Preferably, in the above technical solution, the zinc borate are ultra-fine powders with a particle size of 0.02-0.04 um.
- Preferably, in the above technical solution, the aluminum hydroxide are ultra-fine powders with a particle size of 0.03-0.05 um.
- Further, in the above technical solution, a preparation method of the modified composite flame retardants is as follows: mixing the composite flame retardants with the modifier, and stirring evenly.
- Further, in the above technical solution, the functional modified styrene-acrylic latex is prepared through steps of:
- according to a proportion, adding dicyclopentenyl methacrylate, water, sodium dodecyl sulfate and nonylphenol polyoxyethylene ether into a reactor 1, stirring evenly; adding trimethylene carbonate, after stirring evenly, successively adding acrylic acid, hydroxyethyl acrylate, butyl acrylate and styrene into reaction system, stirring at a constant speed until mixing well; thereafter, heating the reaction system to 70-90°C, adding sodium bicarbonate and a initiator, under stirring condition, a reaction is carried out at constant temperature for 2-4 hours, upon completion of the reaction, cooling to a room temperature, filtering, adjusting a pH value of an obtained product to neutral, and obtaining the functional modified styrene-acrylic latex.
- Further, in the above technical solution, a weight ratio of the dicyclopentenyl methacrylate, the water, the sodium dodecyl sulfate, the nonylphenol polyoxyethylene ether, the trimethylene carbonate, the acrylic acid, the hydroxyethyl acrylate, the butyl acrylate, the styrene, the sodium bicarbonate and the initiator is 1:40-50:0.2-0.3:0.3-0.4:1-1.3:0.2-0.5:4-6: 25-35:25-35:0.2-0.4:0.4-0.6.
- Preferably, in the above technical solution, the initiator is a persulfate salt, and specifically can be any one of ammonium persulfate, sodium persulfate or potassium persulfate.
- Preferably, in the above technical solution, a pH regulator adopts ammonia water.
-
- More preferably, in the above technical solution, the dicyclopentenyl methacrylate is prepared through steps of:
- according to a proportion, successively adding methacrylic acid, trifluoromethanesulfonic acid and hydroquinone to a reactor 2, after stirring and mixing well, heating to 78-82°C, adding dicyclopentadiene to the reactor 2, mixing well, then heating reaction system to 85-90°C, a reaction is carried out at constant temperature for 3-4 hours, upon completion of the reaction, cooling to a room temperature, adding sodium hydroxide (NaOH) into an obtained product, stirring for 1-2 hours, finally washing an obtained mixture, filtering, distilling, and obtaining the dicyclopentenyl methacrylate.
- Most preferably, in the above technical solution, an agitator speed is 100-500 r/min.
- Most preferably, in the above technical solution, a weight ratio of the methacrylic acid, the trifluoromethanesulfonic acid, the hydroquinone, the dicyclopentadiene and the NaOH is 0.8-1.2:0.002-0.004:0.00006-0.0001:1.5-2.0:0.0015-0.002.
- Further, in the above technical solution, a weight percentage concentration of the long fiber pulp is 3.5-4.5%, a weight percentage concentration of the short fiber pulp is 4-5%, and a weight percentage concentration of the modified wood powdery pulp is 3-5%.
- Further, in the above technical solution, in the bottom layer pulp, a weight ratio of the modified wood powdery pulp to the short fiber pulp is 5-10:95-90.
- Further, in the above technical solution, the modified wood powdery pulp is prepared through modifying wood powders with a swelling agent, and the swelling agent is a mixed alkali; a modification method is as follows: after processing the wood powders with a refiner, successively adding the mixed alkali and water, stirring evenly, then heating an obtained mixture to 70-90°C, and a swelling treatment is carried out at constant temperature for 60-90 minutes to form the modified wood powdery pulp.
- preferably, in the above technical solution, the mixed alkali consists of sodium hydroxide and sodium carbonate; wherein: amounts of each raw material are calculated by weight, wood powders: sodium hydroxide: sodium carbonate=1: 0.01-0.03:0.01-0.03.
- preferably, in the above technical solution, the water used for the swelling agent modifying wood powders adopts dryer condensed water in a double-stacked paper machine, which is used for preparing products of the present invention.
- Further, in the above technical solution, in the top layer pulp, a weight ratio of the long fiber pulp to the short fiber pulp is 80-90:20-10.
- Further, in the above technical solution, a weight ratio of the top layer pulp to the bottom layer pulp is 40-50:60-50.
- Further, in the above technical solution, a ratio of total weight of absolute dry fibers contained in the bottom layer pulp and the top layer pulp to a weight of the coating layer is 1:0.005-0.015.
- A second object of the present invention is to provide a preparation method for the above high-performance environment-friendly kraft liner board, comprising steps of:
- (1) pulping steps
- (i)preparation of a long fiber pulp and a short fiber pulp
deflaking old domestic corrugated boxes with a hydrapulper, separating dregs at a high consistency, then coarse screening for first level three stages, screen sizing to a long fiber coarse pulp and a short fiber coarse pulp; separating the long fiber coarse pulp for first level three stages, removing dregs; successively fine screening obtained fibers for first level three stages, thicking with a multi-disc thickener, refining with a conical refiner, and finally diluting with water to obtain the long fiber pulp, storing in a machine chest for use; successively fine screening the short fiber coarse pulp for first level two stages and refining with the conical refiner, finally diluting with water to obtain the short fiber pulp, storing in a pulp chest for use; - (ii)preparation of a modified wood powdery pulp
processing wood powders with a refiner, successively adding a mixed alkali and water, stirring evenly, heating an obtained mixture to 70-90°C, and a swelling treatment is carried out at constant temperature for 60-90 minutes, so as to soften fibers appropriately and form the modified wood powdery pulp with a weight percentage concentration of 3-5%;
- (i)preparation of a long fiber pulp and a short fiber pulp
- (2) papermaking steps
- according to a proportion, mixing the modified wood powdery pulp and the short fiber pulp obtained through the step (1) uniformly to form a bottom layer pulp, mixing the long fiber pulp and the short fiber pulp uniformly to form a top layer pulp; then flowing the bottom layer pulp and the top layer pulp on wire respectively, adding retention and drainage aids to the approach flow system, double-folding, laminating, pressing, drying, coating, calendering and reeling to obtain the high-performance environment-friendly kraft liner board.
- Further, in the above technical solution, in the step(i), a first-stage pressure screen of the fine screening for first level three stages adopts a micro-slot width pressure screen to remove binders, and a screen slot width is 0.08-0.12 mm.
- Further, in the above technical solution, in the step(i), a weight ratio of absolute dry long fibers in the long fiber coarse pulp obtained by screen sizing to absolute dry short fibers in the short fiber coarse pulp is 30-40:70-60.
- Further, in the above technical solution, in the step(i), the long fiber pulp adopts conical refiners in series to refine the pulp, and adopts a long fiber viscous beating technology, and a beating degree is 28-30 °SR.
- Further, in the above technical solution, in the step(i), a weight percentage concentration of the long fiber pulp is 3.5-4.5%, and a weight percentage concentration of the short fiber pulp is 4-5%.
- Further, in the above technical solution, the water in the step (i) and step (ii) both adopts dryer condensed water in a double-stacked paper machine.
- Further, in the above technical solution, the retention and drainage aids in the step (2) consist of two components: cationic polyacrylamide and silica sol, wherein: a weight ratio of absolute dry fibers, cationic polyacrylamide, and silica sol is 1:0.001-0.002:0.001-0.002; the absolute dry fibers refer to total amounts of absolute dry fibers contained in the bottom layer pulp and the top layer pulp.
- Further, in the above technical solution, the coating in the step (2) adopts the metering roller coating technology, specifically, by a metering roller coating method, coating the flame retardant styrene-acrylic latex on the top layer of the kraft liner board obtained through double-folding, laminating, pressing and drying, so as to form a coating layer.
- Compared with the prior art, the beneficial effects of the present invention are described as follows:
- (1) The present invention adopts composite flame retardant latex metering roller coating method to add the flame retardants, which is no loss and low cost, moreover, the addition of the flame retardants has no adverse effects on the strength of the paper.
- (2)The present invention adopts acrylic acid, hydroxyethyl acrylate, butyl acrylate, styrene as reactive monomers, adopts trimethylene carbonate, dicyclopentenyl methacrylate as functional monomers, and adopts a emulsion polymerization method to prepare the functional modified styrene-acrylic latex, then combines it with the flame retardants to prepare the flame retardant styrene-acrylic latex; thereafter, through coating method to prepare the high-performance environment-friendly kraft liner board. The functional modified styrene-acrylic latex of the present invention can replace or partially replace the reinforcing agent, sizing agent and other auxiliary agents added in the pulp during production of the kraft liner board, so that the product has good overall physical strength and water resistance. Moreover, the present invention adopts the metering roller coating method, which improves the smoothness of the surface of the kraft liner board product, greatly improves the printing effect, and raises the level of the product.
- (3) The functional modified styrene-acrylic latex prepared by the present invention is combined with the composite flame retardants containing multiple flame retardant elements to obtain the flame retardant latex, which can fully exert the synergistic flame retardant effect of the multiple flame retardants.
- (4) The preparation process of the present invention is advanced, pollution-free and low production cost, moreover, the prepared kraft liner board has good physical strength, water resistance and flame retardancy. Because the kraft box preparation product of the present invention is produced from all waste paper, the process is environment-friendly and the functional modified styrene-acrylic latex is a water-soluble latex without organic solvents, which improves environmental protection.
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FIG. 1 is a preparation process flow chart of the high-performance environment-friendly kraft liner board according to the present invention. - The present invention is further illustrated in detail with examples. The examples are implemented on the premise of the technology according to the present invention. Now detailed implementation and specific operation process are given to illustrate the creativity of the present invention, but the protection scope of the present invention is not limited to the following examples.
- Based on the information contained in this application, it is easy for those skilled in the art to make various changes to the precise description of the present invention without departing from the spirit and scope of the appended claims. It should be understood that the scope of the present invention is not limited to the defined processes, properties, or components, because these examples and other descriptions are merely intended to illustrate specific aspects of the present invention. In fact, various changes that can be made to the examples of the present invention by those skilled in the art or related fields are all encompassed in the scope of the appended claims.
- In order to better understand the present invention without limiting the scope of the present invention, all numbers expressing dosages, percentages, and other numerical values used in this application should be understood as modified by the word "about" in all cases. Therefore, unless otherwise specified, the numerical parameters listed in the specification and the appended claims are approximate values, which may be changed according to the desired properties that are attempted to be obtained. Each numerical parameter should at least be regarded as obtained based on the reported significant figures and through conventional rounding methods.
- The materials and reagents used in the following examples can be obtained from commercial sources unless otherwise specified.
- In this example, the method for preparing a high-performance environment - friendly kraft liner board, comprising following steps of:
- (1) preparing for a flame retardant styrene-acrylic latex
- (a) preparing for a dicyclopentenyl methacrylate
according to a proportion, successively adding methacrylic acid, trifluoromethanesulfonic acid and hydroquinone to a reactor 2 equipped with an agitator, controlling an agitator speed of the agitator to 210 r/min, after stirring and mixing well, heating to 80°C; then adding dicyclopentadiene, controlling a reaction temperature of reaction system to 85°C, a reaction is carried out at constant temperature for 3.5 hours, upon completion of the reaction, cooling to a room temperature, adding NaOH and stirring for 1.5 hours, washing an obtained mixture, filtering, distilling, and obtaining the dicyclopentenyl methacrylate; wherein: the weight ratio of the methacrylic acid, the trifluoromethanesulfonic acid, the hydroquinone, the dicyclopentadiene, and the NaOH is 1:0.0028:0.000095: 1.72:0.0018; - (b)preparing for a functional modified styrene-acrylic latex
the functional modified styrene-acrylic latex is prepared through following method, particularly comprising steps of:- according to a proportion, adding dicyclopentenyl methacrylate obtained in the step(a), water, sodium dodecyl sulfate and nonylphenol polyoxyethylene ether into a reactor 1, stirring evenly; adding trimethylene carbonate, after stirring evenly, successively adding acrylic acid, hydroxyethyl acrylate, butyl acrylate and styrene into reaction system, stirring at a constant speed until mixing well; thereafter, heating the reaction system to 80°C, adding sodium bicarbonate and ammonium persulfate, under stirring condition, a reaction is carried out at constant temperature for 4 hours, upon completion of the reaction, cooling to a room temperature, filtering, adjusting a pH value of an obtained product to neutral with aqueous ammonia solution, and obtaining the functional modified styrene-acrylic latex;
- wherein: a weight ratio of the dicyclopentenyl methacrylate, the water, the sodium dodecyl sulfate, the nonylphenol polyoxyethylene ether, the trimethylene carbonate, the acrylic acid, the hydroxyethyl acrylate, the butyl acrylate, the styrene, the sodium bicarbonate and the ammonium persulfate is 1:40:0.2:0.3:1:0.2:4:25:25:0.2:0.4;
- (c)preparing for the flame retardant styrene-acrylic latex
mixing modifier N-(β-aminoethyl)-r-aminopropyltrimethoxysilane and composite flame retardants at a weight ratio of 0.002:1, stirring evenly, and obtaining modified composite flame retardants; then mixing the modified composite flame retardants and the functional modified styrene-acrylic latex prepared in the step (a) uniformly at a weight ratio of 1:2.5, diluting with water, and obtaining the flame retardant styrene-acrylic latex with a weight percentage concentration of 2.0%; the water adopts dryer condensed water;
wherein: the composite flame retardants consist of zinc borate and aluminum hydroxide with a weight ratio of 1:1; the zinc borate and aluminum hydroxide are both ultra-fine powders, and a particle size of the zinc borate is 0.02-0.04 um; a particle size of the aluminum hydroxide is 0.03-0.05 um;
- (a) preparing for a dicyclopentenyl methacrylate
- (2) pulping steps
- (i) preparation of a long fiber pulp and a short fiber pulp
deflaking old domestic corrugated boxes with a hydrapulper, separating dregs at a high consistency, then coarse screening for first level three stages, screen sizing to a long fiber coarse pulp and a short fiber coarse pulp; separating the long fiber coarse pulp for first level three stages, removing dregs; successively fine screening obtained fibers for first level three stages, thicking with a multi-disc thickener, refining with a conical refiner, and finally diluting with water to obtain the long fiber pulp, storing in a machine chest for use; successively fine screening the short fiber coarse pulp for first level two stages and refining with the conical refiner, finally diluting with water to obtain the short fiber pulp, storing in a pulp chest for use; the water used in this step all adopts dryer condensed water in a double-stacked paper machine;
wherein: a first-stage pressure screen of the fine screening for first level three stages adopts a micro-slot width pressure screen to remove binders, and a screen slot width is 0.08-0.12 mm;
a weight ratio of absolute dry long fibers in the long fiber coarse pulp obtained by screen sizing to absolute dry short fibers in the short fiber coarse pulp is 40:60;
the long fiber pulp adopts conical refiners in series to refine the pulp, and adopts a long fiber viscous beating technology, and a beating degree is 28 °SR;
a weight percentage concentration of the long fiber pulp is 3.5%, and a weight percentage concentration of the short fiber pulp is 5%; - (ii)preparation of a modified wood powdery pulp
processing wood powders with a refiner, successively adding a mixed alkali and water, stirring evenly, heating an obtained mixture to 70°C, and a swelling treatment is carried out at constant temperature for 60 minutes, so as to soften fibers appropriately and form the modified wood powdery pulp with a weight percentage concentration of 3%;
wherein: the mixed alkali consists of sodium hydroxide and sodium carbonate; the water adopts dryer condensed water in a double-stacked paper machine;
in the step (ii), amounts of each raw material are calculated by weight, wood powders: sodium hydroxide: sodium carbonate=1:0.01:0.01;
- (i) preparation of a long fiber pulp and a short fiber pulp
- (3) papermaking steps
mixing the modified wood powdery pulp and the short fiber pulp obtained in the step (2) uniformly at a weight ratio of 10:90 to form a bottom layer pulp; mixing the long fiber pulp and the short fiber pulp obtained in the step (3) uniformly at a weight ratio of 80:20 to form a top layer pulp; then flowing the bottom layer pulp and the top layer pulp on wire respectively, adding retention and drainage aids to the approach flow system, double-folding, laminating, pressing, drying, coating, calendering and reeling to obtain the high-performance environment-friendly kraft liner board;
wherein: a weight ratio of the top layer pulp to the bottom layer pulp is 40:60;
the retention and drainage aids consist of two components: cationic polyacrylamide and silica sol, a weight ratio of absolute dry fibers, cationic polyacrylamide, and silica sol is 1:0.001:0.001; the absolute dry fibers refer to total amounts of absolute dry fibers contained in the bottom layer pulp and the top layer pulp;
the coating process adopts the metering roller coating technology, specifically, by a metering roller coating method, coating the flame retardant styrene-acrylic latex on the top layer of the kraft liner board obtained through double-folding, laminating, pressing and drying, so as to form a coating layer;
a ratio of the total weight of the absolute dry fibers contained in the bottom layer pulp and the top layer pulp to a weight of the coating layer is 1:0.005. - In this example, the preparation method of a high-performance environment - friendly kraft liner board, comprising following steps of:
- (1) preparing for a flame retardant styrene-acrylic latex
- (a) preparing for a dicyclopentenyl methacrylate
according to a proportion, successively adding methacrylic acid, trifluoromethanesulfonic acid and hydroquinone to a reactor 2 equipped with an agitator, after stirring and mixing well under 100 r/min condition, heating to 78°C; then adding dicyclopentadiene into the reactor 2, mixing well, heating reaction system to 90°C, a reaction is carried out at constant temperature for 3 hours, upon completion of the reaction, cooling to a room temperature, adding NaOH into an obtained product, stirring for 1h, finally washing an obtained mixture, filtering, distilling, and obtaining the dicyclopentenyl methacrylate; wherein: the weight ratio of the methacrylic acid, the trifluoromethanesulfonic acid, the hydroquinone, the dicyclopentadiene, and the NaOH is 0.8:0.002:0.00006: 1.5:0.0015; - (b)preparing for a functional modified styrene-acrylic latex
the functional modified styrene-acrylic latex is prepared through following method, particularly comprising steps of:- according to a proportion, adding dicyclopentenyl methacrylate obtained in the step(a), water, sodium dodecyl sulfate and nonylphenol polyoxyethylene ether into a reactor 1, stirring evenly; adding trimethylene carbonate, after stirring evenly, successively adding acrylic acid, hydroxyethyl acrylate, butyl acrylate and styrene into reaction system, stirring at a constant speed until mixing well; thereafter, heating the reaction system to 70°C, adding sodium bicarbonate and ammonium persulfate, under stirring condition, a reaction is carried out at constant temperature for 3 hours, upon completion of the reaction, cooling to a room temperature, filtering, adjusting a pH value of an obtained product to neutral with aqueous ammonia solution, and obtaining the functional modified styrene-acrylic latex;
- wherein: a weight ratio of the dicyclopentenyl methacrylate, the water, the sodium dodecyl sulfate, the nonylphenol polyoxyethylene ether, the trimethylene carbonate, the acrylic acid, the hydroxyethyl acrylate, the butyl acrylate, the styrene, the sodium bicarbonate and the ammonium persulfate is 1:45:0.25:0.35:1.2:0.3:5:30:30:0.3:0.5;
- (c)preparing for the flame retardant styrene-acrylic latex
mixing modifier N-(β-aminoethyl)-r-aminopropyltrimethoxysilane and composite flame retardants at a weight ratio of 0.005:1, stirring evenly, and obtaining modified composite flame retardants; then mixing the modified composite flame retardants and the functional modified styrene-acrylic latex prepared in the step (a) uniformly at a weight ratio of 1:2.8, diluting with water, and obtaining the flame retardant styrene-acrylic latex with a weight percentage concentration of 3.5%; the water adopts dryer condensed water in a double-stacked paper machine;
wherein: the composite flame retardants consist of ammonium polyphosphate, polyphosphoester and zinc borate with a weight ratio of 1:1:1; the zinc borate are ultra-fine powders, and a particle size of the zinc borate is 0.02-0.04 um;
- (a) preparing for a dicyclopentenyl methacrylate
- (2) pulping steps
- (i) preparation of a long fiber pulp and a short fiber pulp
deflaking old domestic corrugated boxes with a hydrapulper, separating dregs at a high consistency, then coarse screening for first level three stages, screen sizing to a long fiber coarse pulp and a short fiber coarse pulp; separating the long fiber coarse pulp for first level three stages, removing dregs; successively fine screening obtained fibers for first level three stages, thicking with a multi-disc thickener, refining with a conical refiner, and finally diluting with water to obtain the long fiber pulp, storing in a machine chest for use; successively fine screening the short fiber coarse pulp for first level two stages and refining with the conical refiner, finally diluting with water to obtain the short fiber pulp, storing in a pulp chest for use; the water used in this step all adopts dryer condensed water in a double-stacked paper machine;
wherein: a first-stage pressure screen of the fine screening for first level three stages adopts a micro-slot width pressure screen to remove binders, and a screen slot width is 0.08-0.12 mm;
a weight ratio of absolute dry long fibers in the long fiber coarse pulp obtained by screen sizing to absolute dry short fibers in the short fiber coarse pulp is 30:70;
the long fiber pulp adopts conical refiners in series to refine the pulp, and adopts a long fiber viscous beating technology, and a beating degree is 30 °SR;
a weight percentage concentration of the long fiber pulp is 4.0%, and a weight percentage concentration of the short fiber pulp is 4.5%; - (ii)preparation of a modified wood powdery pulp
processing wood powders with a refiner, successively adding a mixed alkali and water, stirring evenly, heating an obtained mixture to 90°C, and a swelling treatment is carried out at constant temperature for 70 minutes, so as to soften fibers appropriately and form the modified wood powdery pulp with a weight percentage concentration of 4%;
wherein: the mixed alkali consists of sodium hydroxide and sodium carbonate; the water adopts dryer condensed water in a double-stacked paper machine;
in the step (ii), amounts of each raw material are calculated by weight, wood powders: sodium hydroxide: sodium carbonate=1:0.02:0.02;
- (i) preparation of a long fiber pulp and a short fiber pulp
- (3) papermaking steps
mixing the modified wood powdery pulp and the short fiber pulp obtained in the step (2) uniformly at a weight ratio of 5:95 to form a bottom layer pulp; mixing the long fiber pulp and the short fiber pulp obtained in the step (3) uniformly at a weight ratio of 90:10 to form a top layer pulp; then flowing the bottom layer pulp and the top layer pulp on wire respectively, adding retention and drainage aids to the approach flow system, double-folding, laminating, pressing, drying, coating, calendering and reeling to obtain the high-performance environment-friendly kraft liner board;
wherein: a weight ratio of the top layer pulp to the bottom layer pulp is 50:50;
the retention and drainage aids consist of two components: cationic polyacrylamide and silica sol, wherein: a weight ratio of absolute dry fibers, cationic polyacrylamide, and silica sol is 1:0.0015:0.0015; the absolute dry fibers refer to total amounts of absolute dry fibers contained in the bottom layer pulp and the top layer pulp;
the coating process adopts the metering roller coating technology, specifically, by a metering roller coating method, coating the flame retardant styrene-acrylic latex on the top layer of the kraft liner board obtained through double-folding, laminating, pressing and drying, so as to form a coating layer;
a ratio of the total weight of the absolute dry fibers contained in the bottom layer pulp and the top layer pulp to a weight of the coating layer is 1:0.01. - In this example, the preparation method of a high-performance environment - friendly kraft liner board, comprising following steps of:
(1) prepareing for a flame retardant styrene-acrylic latex - (a) prepareing for a dicyclopentenyl methacrylate
according to a proportion, successively adding methacrylic acid, trifluoromethanesulfonic acid and hydroquinone to a reactor 2 equipped with an agitator, after stirring and mixing well under 500 r/min condition, heating to 82°C; then adding dicyclopentadiene into the reactor 2, mixing well, heating reaction system to 85°C, a reaction is carried out at constant temperature for 4 hours, upon completion of the reaction, cooling to a room temperature, adding NaOH into an obtained product, stirring for 2 hours, finally washing an obtained mixture, filtering, distilling, and obtaining the dicyclopentenyl methacrylate; wherein: the weight ratio of the methacrylic acid, the trifluoromethanesulfonic acid, the hydroquinone, the dicyclopentadiene, and the NaOH is 1.2:0.004:0.0001: 2.0:0.002; - (b)preparing for a functional modified styrene-acrylic latex
the functional modified styrene-acrylic latex is prepared through following method, particularly comprising steps of:- according to a proportion, adding dicyclopentenyl methacrylate obtained in the step(a), water, sodium dodecyl sulfate and nonylphenol polyoxyethylene ether into a reactor 1, stirring evenly; adding trimethylene carbonate, after stirring evenly, successively adding acrylic acid, hydroxyethyl acrylate, butyl acrylate and styrene into reaction system, stirring at a constant speed until mixing well; thereafter, heating the reaction system to 85°C, adding sodium bicarbonate and ammonium persulfate, under stirring condition, a reaction is carried out at constant temperature for 2 hours, upon completion of the reaction, cooling to a room temperature, filtering, adjusting a pH value of an obtained product to neutral with aqueous ammonia solution, and obtaining the functional modified styrene-acrylic latex;
- wherein: a weight ratio of the dicyclopentenyl methacrylate, the water, the sodium dodecyl sulfate, the nonylphenol polyoxyethylene ether, the trimethylene carbonate, the acrylic acid, the hydroxyethyl acrylate, the butyl acrylate, the styrene, the sodium bicarbonate and the ammonium persulfate is 1:50:0.3:0.4:1.3:0.5:6:35:35: 0.4:0.6;
- (c)preparing for the flame retardant styrene-acrylic latex
mixing modifier N-(β-aminoethyl)-r-aminopropyltrimethoxysilane and composite flame retardants at a weight ratio of 0.01:1, stirring evenly, and obtaining modified composite flame retardants; then mixing the modified composite flame retardants and the functional modified styrene-acrylic latex prepared in the step (a) uniformly at a weight ratio of 1:3.0, diluting with water, and obtaining the flame retardant styrene-acrylic latex with a weight percentage concentration of 5%; the water adopts dryer condensed water in a double-stacked paper machine;
wherein: the composite flame retardants consist of ammonium polyphosphate, polyphosphoester and melamine polyphosphate with a weight ratio of 1:1:1; - (i) preparation of a long fiber pulp and a short fiber pulp
deflaking old domestic corrugated boxes with a hydrapulper, separating dregs at a high consistency, then coarse screening for first level three stages, screen sizing to a long fiber coarse pulp and a short fiber coarse pulp; separating the long fiber coarse pulp for first level three stages, removing dregs; successively fine screening obtained fibers for first level three stages, thicking with a multi-disc thickener, refining with a conical refiner, and finally diluting with water to obtain the long fiber pulp, storing in a machine chest for use; successively fine screening the short fiber coarse pulp for first level two stages and refining with the conical refiner, finally diluting with water to obtain the short fiber pulp, storing in a pulp chest for use; the water used in this step all adopts dryer condensed water in a double-stacked paper machine;
wherein: a first-stage pressure screen of the fine screening for first level three stages adopts a micro-slot width pressure screen to remove binders, and a screen slot width is 0.08-0.12 mm;
a weight ratio of absolute dry long fibers in the long fiber coarse pulp obtained by screen sizing to absolute dry short fibers in the short fiber coarse pulp is 35:65;
the long fiber pulp adopts conical refiners in series to refine the pulp, and adopts a long fiber viscous beating technology, and a beating degree is 30 °SR;
a weight percentage concentration of the long fiber pulp is 4.5%, and a weight percentage concentration of the short fiber pulp is 5%; - (ii)preparation of a modified wood powdery pulp
processing wood powders with a refiner, successively adding a mixed alkali and water, stirring evenly, heating an obtained mixture to 80°C, and a swelling treatment is carried out at constant temperature for 90 minutes, so as to soften fibers appropriately and form the modified wood powdery pulp with a weight percentage concentration of 5%;
wherein: the mixed alkali consists of sodium hydroxide and sodium carbonate; the water adopts dryer condensed water in a double-stacked paper machine;
in the step (ii), amounts of each raw material are calculated by weight, wood powders: sodium hydroxide: sodium carbonate=1:0.03:0.03;
mixing the modified wood powdery pulp and the short fiber pulp obtained in the step (2) uniformly at a weight ratio of 8:92 to form a bottom layer pulp; mixing the long fiber pulp and the short fiber pulp obtained in the step (3) uniformly at a weight ratio of 85:15 to form a top layer pulp; then flowing the bottom layer pulp and the top layer pulp on wire respectively, adding retention and drainage aids to the approach flow system, double-folding, laminating, pressing, drying, coating, calendering and reeling to obtain the high-performance environment-friendly kraft liner board;
wherein: a weight ratio of the top layer pulp to the bottom layer pulp is 45:55;
the retention and drainage aids consist of two components: cationic polyacrylamide and silica sol, wherein: a weight ratio of absolute dry fibers, cationic polyacrylamide, and silica sol is 1:0.002:0.002; the absolute dry fibers refer to total amounts of absolute dry fibers contained in the bottom layer pulp and the top layer pulp;
the coating process adopts the metering roller coating technology, specifically, by a metering roller coating method, coating the flame retardant styrene-acrylic latex on the top layer of the kraft liner board obtained through double-folding, laminating, pressing and drying, so as to form a coating layer;
a ratio of the total weight of the absolute dry fibers contained in the bottom layer pulp and the top layer pulp to a weight of the coating layer is 1:0.015.
The main performance indexes of the high-performance environment-friendly kraft liner board prepared in the examples 1 to 3 are tested. The ring pressure index is tested according to an
Technical indexes | Example 1 | Example 2 | Example 3 |
a basis weight (g/m2) | 100 | 120 | 110 |
a ring pressure index (mN·m2/g) | 6.7 | 7.6 | 7.2 |
a frontal water absorption (g/m2) | 30 | 31 | 30.6 |
flame retardancy (a limit oxygen index %) | 30 | 33 | 32.4 |
a smoothness (seconds) | 15 | 16 | 16 |
a bursting index (kPa·m2/g) | 2.4 | 2.6 | 2.55 |
a folding endurance (times) | 15 | 20 | 20 |
Claims (9)
- A high-performance environment-friendly kraft liner board, comprising a bottom layer, a top layer and a coating layer, which are arranged successively in an order from bottom to top; wherein: the bottom layer is made of a bottom layer pulp composed of a modified wood powdery pulp and a short fiber pulp; the top layer is made of a top layer pulp composed of a long fiber pulp and a short fiber pulp; the coating layer is formed through coating a flame retardant styrene-acrylic latex on the top layer; the long fiber pulp and the short fiber pulp are formed through pulping old domestic corrugated boxes; the flame retardant styrene-acrylic latex consists of modified composite flame retardants, a functional modified styrene-acrylic latex and water;
the functional modified styrene-acrylic latex is prepared through steps of:
according to a proportion, adding dicyclopentenyl methacrylate, water, sodium dodecyl sulfate and nonylphenol polyoxyethylene ether into a reactor 1, stirring evenly; adding trimethylene carbonate, after stirring evenly, successively adding acrylic acid, hydroxyethyl acrylate, butyl acrylate and styrene into reaction system, stirring at a constant speed until mixing well; thereafter, heating the reaction system to 70-90°C, adding sodium bicarbonate and a initiator, under stirring condition, a reaction is carried out at constant temperature for 2-4 hours, upon completion of the reaction, cooling to a room temperature, filtering, adjusting a pH value of an obtained product to neutral, and obtaining the functional modified styrene-acrylic latex. - The high-performance environment-friendly kraft liner board, as recited in claim 1, wherein: a basis weight of the high-performance environment-friendly kraft liner board is100-120 g/m2, a ring pressure index is 6.7-7.6 mN·m2/g, a frontal water absorption is 30-31 g/m2, and a limit oxygen index is 30-33%, a smoothness is 15-16 seconds, a bursting index is 2.4-2.6 kPa·m2/g, and a folding endurance is 15-20 times.
- The high-performance environment-friendly kraft liner board, as recited in claim 1, wherein: a weight ratio of the modified composite flame retardants to the functional modified styrene-acrylic latex is 1:2.5-3.0; the modified composite flame retardants are prepared through modifying composite flame retardants with a silane coupling agent.
- The high-performance environment-friendly kraft liner board, as recited in claim 3, wherein: the composite flame retardants are a combination of any two or more of ammonium polyphosphate, polyphosphoester, melamine polyphosphate, zinc borate, and aluminum phosphate.
- The high-performance environment-friendly kraft liner board, as recited in claim 5, wherein: the dicyclopentenyl methacrylate is prepared through steps of:
according to a proportion, successively adding methacrylic acid, trifluoromethanesulfonic acid and hydroquinone to a reactor 2, after stirring and mixing well, heating to 78-82°C, adding dicyclopentadiene to the reactor 2, mixing well, then heating reaction system to 85-90°C, a reaction is carried out at constant temperature for 3-4 hours, upon completion of the reaction, cooling to a room temperature, adding sodium hydroxide into an obtained product, stirring for 1-2 hours, finally washing an obtained mixture, filtering, distilling, and obtaining the dicyclopentenyl methacrylate; and the trifluoromethanesulfonic acid, the hydroquinone, the dicyclopentadiene and the NaOH is 0.8-1.2:0.002-0.004:0.00006-0.0001: 1.5-2.0:0.0015-0.002. - The high-performance environment-friendly kraft liner board, as recited in claim 5, wherein: a weight ratio of the dicyclopentenyl methacrylate, the water, the sodium dodecyl sulfate, the nonylphenol polyoxyethylene ether, the trimethylene carbonate, the acrylic acid, the hydroxyethyl acrylate, the butyl acrylate, the styrene, the sodium bicarbonate, and the initiator is 1:40-50:0.2-0.3:0.3-0.4:1-1.3:0.2-0.5:4-6:25-35:25-35:0.2-0.4:0.4-0.6.
- The high-performance environment-friendly kraft liner board, as recited in claim 1, the modified wood powdery pulp is prepared through modifying wood powders with a swelling agent, and the swelling agent is a mixed alkali; a modification method is as follows: after processing the wood powders with a refiner, successively adding the mixed alkali and water, stirring evenly, then heating an obtained mixture to 70-90°C, and a swelling treatment is carried out at constant temperature for 60-90 minutes to form the modified wood powdery pulp; wherein: the mixed alkali consists of sodium hydroxide and sodium carbonate.
- A preparation method for the high-performance environment-friendly kraft liner board as recited in claim 1, wherein: comprising steps of:(1) pulping steps(i)preparation of a long fiber pulp and a short fiber pulp
deflaking old domestic corrugated boxes with a hydrapulper, separating dregs at a high consistency, then coarse screening for first level three stages, screen sizing to a long fiber coarse pulp and a short fiber coarse pulp; separating the long fiber coarse pulp for first level three stages, removing dregs; successively fine screening obtained fibers for first level three stages, thicking with a multi-disc thickener, refining with a conical refiner, and finally diluting with water to obtain the long fiber pulp, storing in a machine chest for use; successively fine screening the short fiber coarse pulp for first level two stages and refining with the conical refiner, finally diluting with water to obtain the short fiber pulp, storing in a pulp chest for use;(ii)preparation of a modified wood powdery pulp
processing wood powders with a refiner, successively adding a mixed alkali and water, stirring evenly, heating an obtained mixture to 70-90°C, and a swelling treatment is carried out at constant temperature for 60-90 minutes, so as to soften fibers appropriately and form the modified wood powdery pulp with a weight percentage concentration of 3-5%;(2) papermaking steps
according to a proportion, mixing the modified wood powdery pulp and the short fiber pulp obtained through the step (1) uniformly to form a bottom layer pulp, mixing the long fiber pulp and the short fiber pulp uniformly to form a top layer pulp; then flowing the bottom layer pulp and the top layer pulp on wire respectively, adding retention and drainage aids to the approach flow system, double-folding, laminating, pressing, drying, coating, calendering and reeling to obtain the high-performance environment-friendly kraft liner board. - The preparation method for the high-performance environment-friendly kraft liner board as recited in claim 8, wherein: the coating in the step (2) adopts a metering roller coating method, coating the flame retardant styrene-acrylic latex on the top layer of the kraft liner board obtained through double-folding, laminating, pressing and drying, so as to form a coating layer.
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