JPS62125097A - Production of paper strip impregnated with synthetic resin in solution or dispersion form - Google Patents
Production of paper strip impregnated with synthetic resin in solution or dispersion formInfo
- Publication number
- JPS62125097A JPS62125097A JP61274248A JP27424886A JPS62125097A JP S62125097 A JPS62125097 A JP S62125097A JP 61274248 A JP61274248 A JP 61274248A JP 27424886 A JP27424886 A JP 27424886A JP S62125097 A JPS62125097 A JP S62125097A
- Authority
- JP
- Japan
- Prior art keywords
- dispersion
- paper
- agent
- mixture
- coating
- 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
- 239000006185 dispersion Substances 0.000 title claims abstract description 47
- 229920003002 synthetic resin Polymers 0.000 title claims abstract description 12
- 239000000057 synthetic resin Substances 0.000 title claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- 239000000835 fiber Substances 0.000 claims abstract description 7
- 239000002245 particle Substances 0.000 claims abstract description 4
- 238000002156 mixing Methods 0.000 claims abstract 2
- 239000000123 paper Substances 0.000 claims description 46
- 239000000203 mixture Substances 0.000 claims description 39
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 229920001577 copolymer Polymers 0.000 claims description 13
- 239000001913 cellulose Substances 0.000 claims description 11
- 229920002678 cellulose Polymers 0.000 claims description 11
- 239000011248 coating agent Substances 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 238000000576 coating method Methods 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 7
- 238000000227 grinding Methods 0.000 claims description 7
- 239000004094 surface-active agent Substances 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 238000007598 dipping method Methods 0.000 claims description 4
- 230000035515 penetration Effects 0.000 claims description 4
- 239000002023 wood Substances 0.000 claims description 4
- 244000166124 Eucalyptus globulus Species 0.000 claims description 3
- 238000005498 polishing Methods 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 235000008331 Pinus X rigitaeda Nutrition 0.000 claims description 2
- 235000011613 Pinus brutia Nutrition 0.000 claims description 2
- 241000018646 Pinus brutia Species 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- -1 acrylic ester Chemical class 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
- 239000000945 filler Substances 0.000 claims 1
- 230000008595 infiltration Effects 0.000 claims 1
- 238000001764 infiltration Methods 0.000 claims 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 1
- 239000011976 maleic acid Substances 0.000 claims 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 239000003002 pH adjusting agent Substances 0.000 claims 1
- 238000003786 synthesis reaction Methods 0.000 claims 1
- 239000012209 synthetic fiber Substances 0.000 claims 1
- 229920002994 synthetic fiber Polymers 0.000 claims 1
- 238000010345 tape casting Methods 0.000 claims 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
- 238000005470 impregnation Methods 0.000 abstract description 6
- 229920003043 Cellulose fiber Polymers 0.000 abstract 1
- 238000010009 beating Methods 0.000 abstract 1
- 238000002791 soaking Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 239000007788 liquid Substances 0.000 description 17
- 239000010408 film Substances 0.000 description 16
- 238000009472 formulation Methods 0.000 description 16
- 238000010521 absorption reaction Methods 0.000 description 10
- 239000007787 solid Substances 0.000 description 9
- 239000004033 plastic Substances 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- 229920001807 Urea-formaldehyde Polymers 0.000 description 6
- 239000002518 antifoaming agent Substances 0.000 description 4
- 239000002131 composite material Substances 0.000 description 3
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- QNURTFDBHAQRSI-OAHLLOKOSA-N (4r)-3-[4-[[2-[(3-iodophenyl)methyl]-3-oxocyclohexen-1-yl]amino]phenyl]-4-methyl-4,5-dihydro-1h-pyridazin-6-one Chemical compound C[C@@H]1CC(=O)NN=C1C(C=C1)=CC=C1NC(CCCC1=O)=C1CC1=CC=CC(I)=C1 QNURTFDBHAQRSI-OAHLLOKOSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 241001474791 Proboscis Species 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229920006318 anionic polymer Polymers 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 210000001217 buttock Anatomy 0.000 description 1
- 239000011093 chipboard Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000010002 mechanical finishing Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
- 229920003009 polyurethane dispersion Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000001739 rebound effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000011012 sanitization Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000009870 specific binding Effects 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- FBWNMEQMRUMQSO-UHFFFAOYSA-N tergitol NP-9 Chemical compound CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOCCOCCOCCOCCOCCO)C=C1 FBWNMEQMRUMQSO-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
- Reinforced Plastic Materials (AREA)
- Accommodation For Nursing Or Treatment Tables (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野:
本発明は、溶液および分散液の形の合W、樹脂で含攪し
九紙情状体の製造法に関る、。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application: The present invention relates to a process for the production of composites in the form of solutions and dispersions, stirred with resin.
従来の技術:
テレビジョン装置およびラジオ装置のケーシング、オー
ディオ機器ならびに他の家具部材のケーシングをゲラス
テックフィルムで完全に破模る、ことは、常用されてお
シ、公知である。BACKGROUND OF THE INVENTION It is commonly used and known to completely cover the casings of television and radio equipment, audio equipment and other furniture parts with gelastec films.
そのためには、臀に興なる厚ものPvc−フィルムが使
用される。For this purpose, a thick PVC film is used which covers the buttocks.
このpvc−フィルムは、例えば木屑板上に接着され、
引続きこの複合材料から家具工業の原則から家具部材ま
たはケーシングが1つの作業過程で製造される。すなわ
ち、この本N&中には■字形の溝が切り込まれ、次に&
はこの蒋中で折り党まれるかまたは折り曲げられ、こう
して1つの作業過程でケーシング、家具部材等は製造さ
れる。This PVC film is glued onto a wood chipboard, for example, and
Furniture parts or housings are subsequently produced from this composite material in one operation using the principles of the furniture industry. In other words, a ■-shaped groove is cut into the inside of this book N&, and then &.
are folded or folded in this machine, and thus casings, furniture parts, etc. are manufactured in one operation step.
この方法で1賛なことは、折り目でフィルムに表目を作
らないようにる、ことである。この方法での欠点は、書
びPvC−フィルムにその使用前に直接に良好な印刷適
性を得るために相当る、人血処理、例えばコロナ放電処
理を行なわなければならないことにある。One advantage of this method is that the creases do not create scratches on the film. A disadvantage of this method is that the written PvC film must be subjected to a corresponding human blood treatment, for example a corona discharge treatment, directly before its use in order to obtain good printability.
史に、木消板は、なお経済的に許容される結果を達成し
つるために極めて清陳で滑らかな底面を有しなけれはな
らない(薄手フィルムの塗布)。Historically, wood erasers must have a very clean and smooth bottom surface (thin film application) in order to still achieve economically acceptable results.
しかし、特に不利なことは、温度変化が生じる際にPV
C−フィルムが極めて不オリな寸法安定度(伸び一/収
動挙動)を示し、低い後引表強度を示し、僅かな元安定
度を有し、ならひに高い*ti電性および75°C〜8
5℃での軟化を既に生じる9とである。更に、i2o’
c’を越えて加熱る、。際にHCノー分離が起こる。However, a particular disadvantage is that the PV
The C-film exhibits extremely poor dimensional stability (elongation/contraction behavior), low post-stretch strength, low initial stability, exceptionally high *ti conductivity and 75° C~8
9, which already undergoes softening at 5°C. Furthermore, i2o'
Heat beyond c'. In this case, no HC separation occurs.
刊行物、例えば西Vイツ国特許第2550980号明細
誓の記載から、原紙帯状体を&tx川樹用水浴液および
/または水性分散液を用いて吸収帝域での152x液の
吸収rCよって含役る、ことは、公知でおり、この場合
には、少なくとも完全飽和に十分な童を紙帯状体の表面
上に塗布し、引続きこの#;蛍状体を吸収栄職に旦って
案内し、この吸収帝城中で含浸液を他の表面に吸収させ
る。しかし、皮[樹脂浴液は、銀系樹脂、メラミン樹脂
およびフェノール側脂を基質とる、樹脂であり、ホルム
アルデヒドを含Mし、かつ脆い生成物を生じる。From the description in publications, for example US Pat. It is known to apply at least enough fluorophore to the surface of the paper strip to achieve complete saturation, and then to guide the fluorophore into the absorbent layer, The impregnating liquid is absorbed onto other surfaces in this absorption medium. However, the resin bath liquid is a resin based on silver resin, melamine resin, and phenol fat, contains formaldehyde, and produces a brittle product.
この方法の場合には、原紙帯状体を七の製造後に7)!
、2の装置に供給し、それを丹ひ会出し、吸収帯域のよ
うな付加的な表置および乾珠鋏血を使用しながら含浸し
、かつ再び舎取ることが必要とされる。In the case of this method, the base paper strip is produced after 7)!
, it is necessary to feed the two devices, drain it, impregnate it using additional preparations such as absorbent zones and dried blood, and reconstitute it.
史に、この方法の場合、紙様断面に亘っての含&iの分
布は不均一であり、したがって強く含浸る、栄職が僅か
に含浸る、帯域とともに生じ、このことは、紙核の分解
を生じる。Historically, in the case of this method, the distribution of impurities across the paper-like cross-section is non-uniform, thus resulting in strongly impregnated and slightly impregnated bands, which leads to the decomposition of the paper core. occurs.
西ドイツ、+!+特許特許出願公開第30243考含父
を寂け、この含浸をグループレス磯中で行なうことによ
りプラスチック#腎を抄紙機中で装造る、方法が記載さ
れている。しかし、紙帯状体を詳細に示されてない含浸
液でブレス機中で反歯させることは、このM帯状体が既
に予備含浸されている場合にのみ完全であり、したがっ
てすなわちこの場合にも付加的な装丁九を必要とる、。West Germany, +! +Considering Patent Application Publication No. 30243, a method is described in which a plastic #neel is made in a paper machine by carrying out this impregnation in a groupless rock. However, the recoating of the paper strip in a pressing machine with an impregnating liquid, which is not specified in detail, is only complete if this M strip is already preimpregnated, i.e. also in this case. It requires a specific binding.
発明が解決しようとる、問題点:
従って、本発明の課題は、常法で使用される純粋なグラ
スチックの欠点を有さず、その上さらに良好な可読性を
示し、耐水性を市し、浴剤に対る、安定性を七し、なら
びに湿分の作用および温度変化の除に内部強度および良
好な寸法安定性を有る、フィルム状の、合F9.明脂官
有市状材料を得ることである。The problem that the invention seeks to solve: The object of the invention is therefore to provide a solution that does not have the disadvantages of the pure glass used in conventional methods, yet also exhibits better readability, is water resistant and is suitable for bathing. F9. in film form, having excellent stability against agents and internal strength and good dimensional stability against the effects of moisture and temperature changes. The purpose is to obtain Mingjiang government-owned municipal materials.
史に、この帝状拐料は、艷出しされた紙蛍状体それ自体
の製造を除外して、有利な原料物置から経済的な方法で
できるたけ付加的な処理工程なしに製造できなければな
らない。Historically, this material could only be produced in an economical manner from advantageous raw material stores, with as few additional processing steps as possible, excluding the production of the ejected paper phosphor itself. It won't happen.
その上、なお原紙をできるだけ完全に浸鍋させかつ含浸
る、ことは、本発明によれに、適当に塗布装置ないしは
宮浸狭直を選択る、とともに、例えば粉砕状態および粉
砕度、愼維材料の吸収力、含浸混合物ないしは被覆混合
物の性負に対る、多孔度および衣囲荒δ、すなわちその
表面張力、粘度、@電状悪および固体宮童のような紙の
性負を定める場合にのみ与えられるはずである。Moreover, it is also possible according to the invention to soak and impregnate the base paper as completely as possible by selecting a suitable coating device or dipping method and, for example, by determining the grinding state and degree of grinding, the fiber material. When determining the absorption capacity, the properties of the impregnating mixture or the coating mixture, the porosity and the coating roughness δ, i.e. its surface tension, viscosity, @electrification, and properties of the paper such as solid paper. should be given only.
問題点を解決る、だめの手段:
ところで、この問題は、本発明によれは、前記帯状体を
最大65°SRの粉砕度に初伜されている、筒い吸収力
および強度のセルロース混合物から形成し、含浸液が、
7.5〜10の一価を1る、、アニオン性コポリマー水
性分散液およびアニオン性ポリマー水浴液の混合物から
なり、塗布をグルーブレスを用いて抄紙機の乾燥部分内
で実施る、ことによって解決される。丑に一価は8〜9
の闇にある。Alternative means for solving the problem: According to the present invention, the strip is made of a cellulose mixture with high absorbency and strength, which has been milled to a maximum degree of grinding of 65° SR. forming and impregnating liquid,
7.5 to 10, consisting of a mixture of an aqueous anionic copolymer dispersion and an anionic polymer water bath, the application being carried out in the dry section of the paper machine using a grooveless method. be done. The price of the ox is 8-9
In the darkness.
紙常状体のセルロースは、本発明によれば、ユーカリ粥
ーセルロースと、松材硫酸塩−セルロースとから50
: 50〜10:90、特に30:70〜15:l:1
5の比で成り立っている。According to the present invention, the cellulose in paper form is made from eucalyptus gruel-cellulose and pine wood sulfate-cellulose.
: 50-10:90, especially 30:70-15:l:1
It is made up of a ratio of 5.
粉砕度は、特に15〜25°SRの闇にある。The degree of grinding is particularly between 15 and 25°SR.
紙帯状体の繊維材料には、原紙の性5Lを震える、湿式
固化剤および乾式固化剤、沈戚創(定漕剤)、合成側脂
分散液、界面活性剤、看色網および光躯剤のような他の
化学助剤を〆\加る、ことができる。The fiber material of the paper strip contains a wet solidifying agent, a dry solidifying agent, a settling agent, a synthetic side fat dispersion, a surfactant, a coloring net, and a brightening agent, which affect the properties of the base paper. Other chemical auxiliaries such as can be added.
充填★りは、白色顔料、VすえばTiO2、白を、カオ
リンである。The filling is white pigment, V is TiO2, white is kaolin.
絶対乾燥穢維材料に対して1〜5重′SJ.%の社で例
えにポリアミドアミンーエどりロルヒドリン樹脂の形の
ホルムアルデヒド不含の湿式固化剤ならひに絶対礼法繊
維材料に対して1〜20%の伍で、例えばアクリル版エ
ステル−またはスチレン−ブタジェンを基礎とる、合成
側脂分散液の添加および絶対戦慄繊維材料に対してく0
、5%の菫で紙の湿潤性を改善る、ための界■活性剤の
添加は、本発明の軛曲において符に1利であることが判
明した。1 to 5 times SJ. For example, formaldehyde-free wet solidifying agents in the form of polyamide amine-acrylic rolyhydrin resins can be used in amounts of 1 to 20% based on absolute etiquette textile materials, such as acrylic esters or styrene-butadiene. Based on the addition of synthetic side fat dispersion and absolute zero resistance to textile materials.
The addition of a surfactant to improve the wettability of the paper with 5% violet has been found to be of significant benefit in the present invention.
本発明によれは、世」えはアクリル散、アクリル瞭エス
テル、酢酸ビニルおよび/′またはステロールを基礎と
して横取させることができるアニオン性コポリマー水性
分散液を使用る、場合、分散された粒子は、特に0.2
μ未満であり、皮膜に度は、僅かないし中位であり、か
つ低い最低皮膜形成温度は、袴に60°C以下である。According to the present invention, if the world uses aqueous dispersions of anionic copolymers which can be precipitated on the basis of acrylic powders, acrylic esters, vinyl acetate and/or sterols, the dispersed particles , especially 0.2
μ, the degree of film formation is slight to moderate, and the minimum film formation temperature is 60°C or less on the hakama.
分散准のコポリマーと、浴液のコポリマーとの比は、作
用物買に対して符に500:1〜1:1、有利に100
:1〜10:1であり、すなわち浴液1都にヌ寸して分
敢欣5LlO都ないし浴欣1都に対して分散液10部で
ある。The ratio of the copolymer of the dispersion to the copolymer of the bath liquid is between 500:1 and 1:1, preferably 100:1, relative to the active agent.
:1 to 10:1, that is, 10 parts of the dispersion liquid to 1 part of the bath liquid or 1 part of the bath liquid.
また、本発明の範囲内で他のプラスチック、例えばスチ
レンーブタゾエンーコボリマー、ポリウレタン分散液ま
たはポリオレフィン分散液ならひに含浸剤の官公の尿素
−ホルムアルデヒド但(月旨またはメラミン−ホルムア
ルデヒド*i Jonを基礎とる、浸漬用衛脂溶液を添
加る、こともできる。It is also within the scope of the invention to use other plastics, such as styrene-butazoene-copolymers, polyurethane dispersions or polyolefin dispersions, as well as impregnating agents such as urea-formaldehyde or melamine-formaldehyde. It is also possible to add sanitizing solution for dipping.
含浸した紙の脆い性質は、反賀用側崩浴欣全含有る、本
発明による混合物を使用る、ことによって阻止る、こと
ができる。The brittle nature of the impregnated paper can be counteracted by using a mixture according to the invention which contains a sintering agent.
また、この含&薊混合物に湿@剤、柘艮駒企削、付看防
止助剤および次透助刑、顔料、染料および消泡剤のよう
な他の助1t’J 7il−IQ加る、こともできる。In addition, other additives such as wetting agents, anti-foaming agents and antifoaming agents, pigments, dyes and antifoaming agents are also added to this mixture. , can also be done.
湿潤剤および浸透薊としては、欣相と固体相との間の次
面張力を変える物置、例えば界面活性剤および乳化剤が
使用ちれる。As wetting agents and penetrants used are agents which change the surface tension between the liquid phase and the solid phase, such as surfactants and emulsifiers.
本発明によれば、マレイン販−コポリマーと、衣[11
1張力を変える前記物置との組合せ吻によって官授孜の
浸透は有利に調節る、ことができる。According to the present invention, maleic copolymers and clothing [11
1. By changing the tension in combination with the above-mentioned proboscis, the penetration of the permeation can be advantageously regulated.
本発明によれは、この含浸剤は、5〜60%の固体含量
を有る、溶液と分散液とからなる混合物の形で使用され
、この場合粘度は、10〜60 s (DIN−カップ
による、4 m )の間にある。According to the invention, the impregnating agent is used in the form of a mixture of solutions and dispersions with a solids content of 5 to 60%, the viscosity being 10 to 60 s (according to DIN cup). 4 m).
この含浸混合物および被覆混合物を繊m7+)−ス上に
僅布る、ことは、抄紙機内でロール杢布装箇(ダル−ブ
レス機)中で行なわれる。この場合、本発明によれば、
98〜92%の乾保含量を有る、繊維フリースは、ダル
−ブレス機を介して供給され、こうして両側をfflる
、ことは行なわれる。The impregnating mixture and the coating mixture are spread onto the fiber m7+) in a roll press machine in the paper machine. In this case, according to the invention:
The fiber fleece, with a dry content of 98-92%, is fed through a Dull-Bress machine, thus ffling on both sides takes place.
本発明によれば、含浸のこの第1の処理工程後にさらに
m維フリースの片面またに両面ケ表面板復る、ことは、
抄紙機内で同一かまたは同殊に悄成されたコホ′リマー
混合物を用いて行なうことができ、この場合には、2つ
の個々の処理工程のra〕で中間乾燥は行なわなけれは
ならない。According to the invention, after this first treatment step of impregnation, the m-fiber fleece is further coated on one side or on both sides.
This can be carried out in the paper machine using copolymer mixtures which are the same or which are prepared in the same manner, in which case intermediate drying has to be carried out in two separate process steps.
Ifi床した帯状体の片面上にその後に被層を設けるこ
とによって、良好な印刷適性またはラッカー塗布可能性
もしくは被覆可能性を生じる緻密な表面が侍られる。史
に、片面を表面被覆る、場合にのみ、この表面被覆は、
ナイフ堕浦装置を用いて行なうことができる。被覆され
た紙帯状体を片面でロール壁布る、ことは、良問上で付
加的に塗布る、ことによって阻止る、ことができる。By subsequently applying a coating on one side of the Ifi-bedded strip, a dense surface is provided which results in good printability or lacquerability or coatability. Historically, only when one side is surface coated, this surface coating is
This can be done using a knife-dropping device. Rolling the coated paper strip on one side can be prevented by additionally applying a coat on the surface.
このように塗布る、塗料は、例えば散粉またはCMCの
儂厚水浴液であることができる。含浸した、片面を被覆
した帯状体を、例えば公知の機械仕上加工装置を用いる
かまたは別個の作条過程でカレンダー中で付加的に仕上
けることにより、なお抜機した面の所望の印枦」適性お
よびラッカー塗布可能性は上昇る、。The paint applied in this way can be, for example, a powder or a thick water bath of CMC. The impregnated, single-sided coated strip can be additionally finished, for example using known mechanical finishing equipment or in a calender in a separate cutting process, to still achieve the desired marking properties on the cut side. and lacquer application possibilities increase.
このような方法で侍られた、フリース表造の除および反
演し仮積した常状体の仕上けの際に使用された圧力に応
じて兵なる厚さおよび具なる粗密度の前記フィルムは、
袴に比軟的紋賞で剛性の下地、例えば安定な複合物で例
えばテレビジョン装置およびラジオ装置のケーシングま
たはオーディオ機器のケーシング(ケーシンク外被)の
ような家具部材の装飾的保護被覆として適当である。こ
の経済的に南オリに製造しうる繊維含有フィルム全使用
る、ことによって、PVC−フィルムまたは他のプラス
チックフィルムを使用る、際の首記した欠点は回避され
る。Said film, applied in this way, has a specific thickness and a specific density depending on the pressure used during the removal of the fleece surface and the finishing of the reacted and pre-laid normal body. ,
A rigid substrate with a soft emblem on the hakama, for example a stable composite, suitable as a decorative protective covering for furniture parts, such as casings of television and radio equipment or casings of audio equipment (casing shells). be. By using this economically economically producible fiber-containing film, the disadvantages mentioned above when using PVC films or other plastic films are avoided.
高い可読性、温度変化の除の寸法安定性を有しかつ水お
よび溶剤に対して良好な遮断性を有する、本発明により
得られた繊維官有フィルムは、同体に他の目的のために
、例えば湿式研磨用の筒価な研磨紙の基材、印刷担体お
よび広普担体、装*;b用壁材料(例えば、離燃a原料
を含有したかまたは含量してない寸法安定性のテーブル
掛)、粘着チーブ、例えば床張用の支持爪として特に適
当である。The fiber-organized films obtained according to the invention, which have high readability, dimensional stability against temperature changes and good barrier properties against water and solvents, can also be used for other purposes, e.g. Cylindrical abrasive paper substrates for wet polishing, printed carriers and general carriers, wall materials for packaging (e.g. dimensionally stable table hangings with or without combustible raw materials) , are particularly suitable as support nails for adhesive chips, e.g. floor coverings.
実施例: 次に、本発明を実施例につき評祝る、。Example: Next, the present invention will be evaluated with reference to examples.
例1
本発明によれは、次の組成および条件の原紙を二層の紙
として複式抄紙機上で得る:松材硫酸塩−セルロース
80%。Example 1 According to the invention, a base paper with the following composition and conditions is obtained on a duplex paper machine as a two-layer paper: pinewood sulfate-cellulose
80%.
ユーカリ佃−セルロース 20%。Eucalyptus Tsukuda - Cellulose 20%.
粉砕度 30’SR(ショパーーリーダラー(5cho
pper −Rlegler ) ) 。Grinding degree 30'SR (Chopper Leader (5cho)
pper-Rlegler)).
添加剤、市販品(絶対乾燥セルロースに対して計算した
):
メルク 1%。Additives, commercially available (calculated on absolutely dry cellulose): Merck 1%.
ホルムアルデヒド不含の湿式 %式% 湿潤剤および分散剤 [J、3%。Formaldehyde-free wet method %formula% Wetting and dispersing agents [J, 3%.
909/m2の単位面積あたりの1菫を有る、この原紙
を比20:1の分散液と溶成の本発明による合成側脂漏
合物でグループレス機中で内面で含浸した。この本発明
による合成樹脂−混合物を用いて意外なことに、符にこ
の硼合生じる吸水性を考慮しなから層強度および剛性に
より特徴づけられる強い含反効果は、使用される分散液
および′#r故の相乗幼果に確実に基づくものであり、
これらの分散液および浴液は、単独で使用る、と、同様
に意図される良好な紙物性を全く達成る、ことができな
い。This base paper, with 1 violet per unit area of 909/m 2 , was impregnated on the inner side in a groupless machine with a dispersion and an aqueous synthetic seborrheic compound according to the invention in a ratio of 20:1. Surprisingly, with the synthetic resin mixture according to the invention, a strong rebound effect characterized by layer strength and stiffness, even without taking into account the resulting water absorption, is possible due to the dispersion used and the It is definitely based on synergistic young fruits due to #r,
These dispersions and baths, when used alone, also cannot achieve the intended good paper properties at all.
次の例は、この事実を証明る、ものである。The following example proves this fact.
グルー処理液は、部分的に水で最適な粘度(DIN−カ
ップにより<60S、4mm)に調部しなけれはならな
かった。The glue treatment solution had to be adjusted partially with water to an optimal viscosity (<60S, 4 mm by DIN cup).
グループレス機用の処方:
1−合成樹脂一分散液 単独(アクリル敗エステル、ア
クリルニトリルおよびスチロールを基促とる、アニオン
性コポリマー水性分散散)、固体金1t50%、平均粒
径約0.1μ、中位の皮膜硬度、最低皮膜形成温度く1
℃。Formula for groupless machine: 1-Synthetic resin monodispersion alone (anionic copolymer aqueous dispersion based on acrylic ester, acrylonitrile and styrene), solid gold 1t50%, average particle size about 0.1μ, Moderate film hardness, minimum film formation temperature 1
℃.
2−水で希釈したプラスチック分散液、同体言t25%
1
6−水で希釈したプラスチック浴液 単独(無水マレイ
ンCRヲ基礎とる、カル1メキシル基含有コポリマーの
アニオン性水浴液)、固体含量約12%。2-Plastic dispersion diluted with water, t25%
1 6-Plastic bath solution diluted with water alone (anionic water bath solution of cal-1-mexyl group-containing copolymer based on anhydrous maleic CR), solids content approximately 12%.
4−水で希釈した、ホルムアルデヒド不含の湿式固化炸
jを有る、プラスチック溶液、固体含奮約10%。4-Plastic solution diluted with water, formaldehyde-free wet setting explosive, solids content approximately 10%.
5−水で約25%の固体含量に希釈した、ホルムアルデ
ヒげ不含の湿式固化剤および消泡創を添加した、比20
:1の分散液(例1による)と、浴液(例6にょる)と
からなる本発明によるグラスチック混合物。5 - Ratio 20 with addition of formaldehyde-free wet setting agent and defoaming wound diluted with water to about 25% solids content.
: A plastic mixture according to the invention consisting of a dispersion of 1 (according to Example 1) and a bath liquid (according to Example 6).
純粋なプラスチック分散′e、(処方1)は、実際にそ
の良好な皮膜形成特性のために吸水量を最も強く減少さ
せるが、原紙中への浸透は、不十分である。このことは
、層の強度および剛性の点で僅かのみ改善された値によ
って証明される。Pure plastic dispersion 'e, (formulation 1) actually reduces water absorption the most strongly due to its good film-forming properties, but its penetration into the base paper is insufficient. This is evidenced by the only slightly improved values in terms of strength and stiffness of the layer.
この分散液を水で希釈る、こと(処方2)によって、原
紙中への強い浸透は、lHj時に吸水量を上昇させかつ
なお含浸した紙の弾性か不十分である際に行なわれる。By diluting this dispersion with water (formulation 2), a strong penetration into the base paper is achieved when the water absorption increases at lHj and the elasticity of the impregnated paper is still insufficient.
更に、含浸が不十分であることは、峨衣面の梳き強度が
不十分であることにおいて顕者である。原紙を水で布釈
した合成倒脂浴液(処方6)で含浸る、ことは、実際に
数音された弾性を導くが、者しく劣化ちれ71c層頻度
を1ねく。Furthermore, insufficient impregnation is manifested in insufficient combing strength of the dyed surface. Impregnating the base paper with a synthetic antifat bath solution (prescription 6) diluted with water actually leads to improved elasticity, but it also deteriorates significantly and reduces the frequency of the 71c layer.
また、湿式固化剤を添加る、こと(処方4)は、含浸し
た紙の本質的な性質の変化を全く生じない。Also, the addition of a wet setting agent (formulation 4) does not result in any change in the essential properties of the impregnated paper.
処方2の場合よりも約10%だけ高い増強度、比収的低
い吸水量および最高の弾性(処方6の場合よりも約10
%低い剛性)によって特徴づけられる、グルー処理液の
所望の高い含浸効果、ひいては全ての意図した良好な紙
特性は、分散液および溶液の本発明による合成樹脂混合
物(処方5)によって初めて達成される。About 10% higher enhancement, lower specific water absorption and highest elasticity than for formulation 2 (about 10% more than for formulation 6)
The desired high impregnating effect of the glue treatment liquid, characterized by a low stiffness (% low stiffness), and thus all the intended good paper properties, is achieved for the first time with the synthetic resin mixture according to the invention (formulation 5) of dispersions and solutions. .
個々の成分(分散液、溶液、湿式固化Δす)の作用につ
いて予想されない過大に高い前記含は効果は、分散液お
よび浴液の相乗作用に帰る、。The unexpectedly high effect of the effects of the individual components (dispersion, solution, wet solidification) is due to the synergistic effect of the dispersion and bath liquid.
?112
他の一連の試験において、中位の硬度の合成、切脂分散
液(5)を約0.15μの粒往を有する硬質分te、液
によって最低皮膜形成温度約25°Cで交換した。この
分散液は、アクリル液エステルおよびスチロールを基礎
とる、コポリマー水性分散液であった。? 112 In another series of tests, a medium hardness synthetic, cut resin dispersion (5) was replaced by a hard fraction te liquid with a grain size of about 0.15μ at a minimum film formation temperature of about 25°C. The dispersion was an aqueous copolymer dispersion based on acrylic liquid ester and styrene.
この分散液で含浸した原紙の次の性質が侍られた(先行
る、第1の試験から処方5を用いて得られた結果を理解
し易くる、ために丹ひ記載した):
6−ホルムアルデヒド不含の湿式固化★りを添加した、
水で布釈した合成側脂分淑液、固体含量約25%。The following properties of the base paper impregnated with this dispersion were observed (described briefly to facilitate understanding of the results obtained using Formulation 5 from the previous first test): 6-Formaldehyde Wet-cured with no additives,
Synthetic side fat extract diluted with water, solids content approximately 25%.
7−水で約25%の固体含量に希釈した、ホルムアルデ
ヒド不含の湿式固化剤および消泡剤
を添加した、比20:1の分散液とサリ6による浴液と
からなる本発明による合成樹脂混合物。7 - Synthetic resin according to the invention consisting of a dispersion in the ratio 20:1 and a bath liquor according to Sali 6, diluted with water to a solids content of about 25%, with the addition of a formaldehyde-free wet setting agent and an antifoaming agent. blend.
処方6による純粋な合成側脂分敢敵を用いると、処方1
および2の場合にも既に証明されたように意図した高い
含浸効果ii:達成る、ことができない。分散液と溶液
の本発明による組合せ物で初めて丹ひ所望の紙の性質が
尋かれ、この場合選択した分散液の高い皮挨恢度のたり
に言反した紙の弾性は、処方5を使用る、場合よりも恋
い結果となる。Using pure synthetic side fat adversary according to formulation 6, formulation 1
As has already been demonstrated in case 2 and 2, the intended high impregnating effect ii: cannot be achieved. For the first time, the desired paper properties were investigated for the combination according to the invention of dispersion and solution; However, the result is better than the case.
この本発明によシ言反した紙を次に虎出しる、ことによ
って、剛性は約10〜20Xたけ、吸水力は約15〜2
0先たけ減少る、が、層強度は殆んど不変のままである
。Next, the paper that is contrary to the present invention is extracted, so that the stiffness is about 10 to 20 times higher and the water absorption power is about 15 to 2 times higher.
0, but the layer strength remains almost unchanged.
乞」
直ぐ次の試験において、分散液および浴液の本発明によ
る合成側腹混合物を原木−ホルムアルデヒド樹脂との組
合せ物で2:1の比で例1による原紙を含浸る、ために
使用した。In the immediately following tests, the synthetic flank mixture according to the invention of dispersion and bath liquid was used to impregnate base paper according to Example 1 in a ratio of 2:1 with a raw wood-formaldehyde resin combination.
8−1 :2の比で尿素−ホルムアルデヒド樹脂との組
付せ物での処方乙による合成側脂分散液 単独。Synthetic side fat dispersion according to formulation B alone in combination with urea-formaldehyde resin at a ratio of 8-1:2.
9−1 :2の比で尿素樹脂との組合ぜ物で処方7によ
り(比20:1の)分散液と溶液とからなる本発明によ
る合成切崩混合物。Synthetic cutting mixture according to the invention consisting of a dispersion and a solution (in a ratio of 20:1) according to formulation 7 in combination with a urea resin in a ratio of 9-1:2.
10−1:2の比で尿素−ホルムアルデヒド&(脂との
組合せ物で固体金[5o313、平均粒径約0.15μ
、中位の皮膜硬度、厳低皮族形成温度12゛Cを有る、
合成樹脂分散液単独(アクリレートを基質とる、アニオ
ン性コポリマー水性分散液)。Solid gold in combination with urea-formaldehyde & (fat) in a 10-1:2 ratio
, moderate film hardness, extremely low skin formation temperature of 12°C,
Synthetic resin dispersion alone (anionic copolymer aqueous dispersion with acrylate as a substrate).
11−1:2の比で尿素樹脂との組合せ物で比20:1
の分散液(処方10による)と浴液(処方6による)と
からなる本発明による合成樹脂混合物。11-1:2 ratio in combination with urea resin 20:1 ratio
A synthetic resin mixture according to the invention consisting of a dispersion (according to formulation 10) and a bath liquid (according to formulation 6).
含浸した紙の得られた性質は、次表に記載されている:
また、合成樹脂分散液と、例えば尿素−ホルムアルデヒ
ド樹月旨のような浸漬用與月旨(例えば、これは装飾原
紙を別個の含浸装置中で含浸る、ために常用されている
。)との組合せ物は、原紙の性質を改善る、ことを導く
。この場合、使用された合成側脂分散液の型は、不買的
に処理液吸収量、多孔度、吸水量および厭の増強度を定
める(処方8および10参照)。The resulting properties of the impregnated paper are listed in the following table: It is also possible to mix the synthetic resin dispersion and the dipping material, such as urea-formaldehyde material (for example, this can be used to separate the decorative base paper). (commonly used for impregnation in impregnating equipment) leads to improved properties of the base paper. In this case, the type of synthetic side fat dispersion used dictates the processing liquid absorption, porosity, water absorption and degree of water enhancement (see formulations 8 and 10).
しかし、分散液および浴液の本発明による合成m側温合
物によって初めて、この特殊な浸漬用樹脂−合成樹脂−
組合せ物の場合にも所望の高い言浸効果、ひいては含浸
した紙の意図した性質が侍られる(処方9および11び
照)。そのためには、例えば多孔度および吸水量が者し
く減少されることならびに層gi&が上昇る、ことが楓
る、。しかし、比戟的高い&漬用樹脂−含霊のために増
強度の水準は、処方1および2の場合よりも若干低い。However, it is not until the inventive synthetic m-side mixture of dispersions and bath liquids that this special immersion resin - synthetic resin -
The desired high impregnation effect and thus the intended properties of the impregnated paper are also observed in the case of the combination (formulations 9 and 11). For this purpose, for example, the porosity and the water absorption are significantly reduced and the layer gi& is increased. However, the level of enhancement is slightly lower than in formulations 1 and 2 due to the relatively high pickling resin content.
Claims (1)
体を製造する方法において、該帯状体を最大35°SR
の粉砕度に粉砕されている、高い吸収力および強度のセ
ルロース混合物から形成し、含浸液7.5〜10のPH
価を有する、アニオン性コポリマー水性分散液およびア
ニオン性水溶液の混合物からなり、塗布をグループレス
機を用いて抄紙機の乾燥部分内で実施することを特徴と
する、溶液および分散液の形の合成樹脂で含浸した紙帯
状体の製造法。 2、pH価を特に8〜9の範囲に調節する、特許請求の
範囲第1項記載の方法。 3、紙帯状体のセルロースをユーカリ樹−セルロースお
よび松材硫酸塩−セルロースから 50:50〜10:90、特に30:70〜15:85
の比で、場合によつては合成繊維材料との組合せ物で形
成し、15〜25°SRの粉砕度にまで特に裁断粉砕す
る、特許請求の範囲第1項または第2項に記載の方法。 4、紙帯状体の繊維材料にpH−調整剤、湿式固化剤お
よび乾式固化剤、合成樹脂分散液、沈殿剤(定着剤)、
界面活性剤、着色剤、充填剤等のような他の化学助剤を
添加する、特許請求の範囲第1項から第3項までのいず
れか1項に記載の方法。 5、フリース繊維を処理するための浸漬剤ないしは被覆
剤として0.2μ以下の平均粒径、僅かないし中位の皮
膜硬度および30℃以下の最低皮膜形成温度を有するア
クリル酸、アクリル酸エステル、アクリルニトリル、酢
酸ビニルおよび/またはスチロールを基礎とする常用の
アニオン性コポリマー水性分散液を、無水マレイン酸な
いしはマレイン酸と例えばスチロール、アクリル酸、ア
クリル酸エステル等とを100:1〜10:1(作用物
質に対して計算した)、特に25:1〜15:1の比で
基礎とするコポリマーの常用のアニオン性水溶液との組
合せ物で、ならびに他の添加剤、例えば硬化助剤、粘度
調整助剤、付着防止助剤および浸透助剤ならびに顔料お
よび染料と一緒に使用する、特許請求の範囲第1項から
第4項までのいずれか1項に記載の方法。 6、付加的に分散液と溶液とからなる混合物は界面活性
剤の含分を含有する、特許請求の範囲第1項から第4項
までのいずれか1項に記載の方法。 7、界面活性剤の含分は分散液と溶液とからなる混合物
に対して0.05〜1.5%である、特許請求の範囲第
1項から第6項までのいずれか1項に記載の方法。 8、紙帯状体の繊維フリースを浸潤させることは抄紙機
内で第1の処理工程で両側でロール塗布により行なわれ
、被覆することは第2の処理工程で片側でナイフ塗布に
より行なわれ、このナイフ塗布は紙帯状体を表面艶出し
することを接続している、特許請求の範囲第1項から第
7項までのいずれか1項に記載の方法。 9、紙帯状体に乾燥および表面艶出しを行なつた後に片
側の表面後処理、例えば被覆、印刷および/またはラツ
カー塗布を行なう、特許請求の範囲第1項から第8項ま
でのいずれか1項に記載の方法。[Claims] 1. A method for producing paper strips impregnated with synthetic resins in the form of solutions and dispersions, wherein the strips are heated to a maximum of 35°SR.
Formed from a high absorbency and strength cellulose mixture that has been ground to a grinding degree of
Synthesis in the form of solutions and dispersions, consisting of an aqueous anionic copolymer dispersion and a mixture of an anionic aqueous solution, having an anionic aqueous dispersion, characterized in that the application is carried out in the dry section of a paper machine using a groupless machine. Method for manufacturing paper strips impregnated with resin. 2. The method according to claim 1, in which the pH value is adjusted in particular to a range of 8 to 9. 3. The cellulose of the paper strip is prepared from eucalyptus tree-cellulose and pine wood sulfate-cellulose at a ratio of 50:50 to 10:90, especially 30:70 to 15:85.
2, optionally in combination with synthetic fiber materials, and particularly cut and ground to a grinding degree of 15 to 25° SR. . 4. A pH-adjusting agent, a wet solidifying agent, a dry solidifying agent, a synthetic resin dispersion, a precipitant (fixing agent),
4. A method as claimed in any one of claims 1 to 3, in which other chemical auxiliaries such as surfactants, colorants, fillers, etc. are added. 5. Acrylic acid, acrylic ester, or acrylic having an average particle size of 0.2μ or less, a slight to medium film hardness, and a minimum film formation temperature of 30°C or less as a dipping agent or coating agent for treating fleece fibers. Aqueous dispersions of customary anionic copolymers based on nitrile, vinyl acetate and/or styrene are prepared by mixing maleic anhydride or maleic acid with, for example, styrene, acrylic acid, acrylic esters, etc. in a ratio of 100:1 to 10:1 (effect). (calculated for the substance), especially in combination with customary anionic aqueous solutions of the basic copolymers in a ratio of 25:1 to 15:1, as well as other additives, such as hardening aids, viscosity-controlling aids. , in combination with anti-adhesion and penetration aids and pigments and dyes. 6. The method as claimed in claim 1, wherein the mixture of dispersion and solution additionally contains a surfactant content. 7. According to any one of claims 1 to 6, the content of the surfactant is 0.05 to 1.5% based on the mixture consisting of the dispersion and the solution. the method of. 8. The infiltration of the fiber fleece of the paper strip is carried out in the paper machine in a first processing step by roll coating on both sides, and the coating is carried out in a second processing step by knife coating on one side, this knife 8. A method according to claim 1, wherein the application is coupled with surface polishing of the paper strip. 9. One of the claims 1 to 8, wherein the paper strip is subjected to a surface post-treatment on one side after drying and surface polishing, such as coating, printing and/or lacquering. The method described in section.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3541187A DE3541187C2 (en) | 1985-11-21 | 1985-11-21 | Process for producing a paper web impregnated with synthetic resins and their use |
DE3541187.2 | 1985-11-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62125097A true JPS62125097A (en) | 1987-06-06 |
JPH0726355B2 JPH0726355B2 (en) | 1995-03-22 |
Family
ID=6286484
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61274248A Expired - Lifetime JPH0726355B2 (en) | 1985-11-21 | 1986-11-19 | Process for the production of paper strips impregnated with synthetic resin in the form of solutions and dispersions |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP0223922B2 (en) |
JP (1) | JPH0726355B2 (en) |
AT (1) | ATE59416T1 (en) |
CA (1) | CA1329072C (en) |
DD (1) | DD259885A5 (en) |
DE (2) | DE3541187C2 (en) |
ES (1) | ES2000141A6 (en) |
FI (1) | FI86902C (en) |
NO (1) | NO174725C (en) |
PT (1) | PT83153B (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3631835A1 (en) * | 1986-09-19 | 1988-03-24 | Kaemmerer Gmbh | METHOD FOR PRODUCING YELLOW-RESISTANT PAPER, IN PARTICULAR AGAINST HEAT |
DE4413619C2 (en) * | 1993-12-02 | 1996-09-26 | Wkp Wuerttembergische Kunststo | Process for making paper and laminates |
DE19758479C2 (en) * | 1997-07-02 | 2002-07-11 | Koehler Decor Gmbh & Co Kg | impregnating |
DE19728250C2 (en) * | 1997-07-02 | 2002-01-17 | Koehler Decor Gmbh & Co Kg | Process for producing a pre-impregnate, the pre-impregnate obtained therewith and its use for the production of decorative composite structures |
DE19946151C5 (en) * | 1999-09-27 | 2010-02-04 | Koehler Decor Gmbh & Co Kg | Process for the preparation of a prepreg, the prepreg prepared therefrom and its use |
DE10016810A1 (en) * | 2000-04-05 | 2001-10-11 | Basf Ag | Polymer dispersion for impregnating paper |
DE10104820C1 (en) * | 2001-02-01 | 2002-08-08 | Erfurt & Sohn Kg | wall covering |
WO2002079571A1 (en) * | 2001-03-30 | 2002-10-10 | Kronospan Technical Company Ltd. | Paper for producing panels and paper-making method |
DE102008041296A1 (en) | 2007-08-22 | 2009-03-19 | Basf Se | Aqueous impregnating agent, useful for impregnating raw or glued papers, comprises an urea derivative and an emulsion polymer, where the emulsion polymer contains ethylenically unsaturated monomer containing e.g. epoxide group |
NL1036705C2 (en) | 2009-03-13 | 2010-09-14 | Trespa Int Bv | METHOD FOR MANUFACTURING A DECOR PAPER IMPREGNATED WITH A RESIN AND A DECOR PANEL |
DE102009043958A1 (en) * | 2009-09-07 | 2011-03-17 | Michael Wiederschein | Impregnated material and process for producing an impregnated material |
DE102010016864B4 (en) † | 2010-05-10 | 2018-09-27 | Papierfabrik Julius Schulte Söhne GmbH & Co. KG | Fibrous core paper, process for its preparation and its use |
NL2007494C2 (en) | 2011-09-28 | 2013-04-02 | Trespa Int Bv | METHOD FOR MANUFACTURING A DECORATIVE FILM AND A DECOR PANEL |
DE102011122012B4 (en) * | 2011-12-22 | 2017-04-06 | Neenah Gessner Gmbh | Impregnated abrasive base paper, process for producing impregnated abrasive base paper and its use |
DE102013114420A1 (en) | 2012-12-23 | 2014-06-26 | Michael Jokiel | Impregnated paper comprises base paper which is impregnated on one side with water-based impregnating solution comprising e.g. aqueous dispersion of styrene-ethyl-butyl acrylate copolymer and aqueous dispersion of styrene-acrylate copolymer |
NL2011719C2 (en) | 2013-11-01 | 2015-05-04 | Trespa Int Bv | A decorative panel. |
NL2014060B1 (en) | 2014-12-24 | 2016-09-30 | Trespa Int Bv | A method for producing a printed decorative paper. |
CN109489104A (en) * | 2017-09-11 | 2019-03-19 | 南京新莱尔材料科技有限公司 | A kind of fever wallpaper and its manufacturing method for indoor heating |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52143117A (en) * | 1976-05-25 | 1977-11-29 | Tomoegawa Paper Co Ltd | Secondary original drawing paper |
JPS54120713A (en) * | 1978-03-06 | 1979-09-19 | Hoechst Gosei Kk | Treating agent and method for rendering paper transparent |
JPS5742994A (en) * | 1980-06-28 | 1982-03-10 | Letron Gmbh & Co | Production of synthetic substance coated plate |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3026217A (en) * | 1958-04-11 | 1962-03-20 | Kimberly Clark Co | Fiber products and methods of manufacturing comprising base sheet of cellulose fibers saturated with a mixture comprising elastomeric polymer and polar adjunct polymer having carboxylic acid functional group |
GB1358296A (en) * | 1970-07-10 | 1974-07-03 | Bayer Ag | Anionic papersizing agents |
DE2254781C2 (en) * | 1972-11-09 | 1980-10-16 | Roehm Gmbh, 6100 Darmstadt | Use of cationic plastic dispersions for sizing paper |
JPS5324106B2 (en) * | 1974-05-25 | 1978-07-19 | ||
SE417849B (en) * | 1974-11-20 | 1981-04-13 | Billingsfors Bruks Ab | PROCEDURE FOR MANUFACTURING IMPREGNATED AND COATED WRAPPING |
DE2550980C3 (en) * | 1975-11-13 | 1979-12-13 | Roehm Gmbh, 6100 Darmstadt | Method and device for impregnating absorbent base papers |
DE2949306A1 (en) * | 1979-12-07 | 1981-06-11 | Letron GmbH, 8750 Aschaffenburg | Synthetic veneer of paper fibre compsn. impregnated with resin - contg. equal wt. of long and short fibres, can be made on paper machine |
DE3015733C2 (en) * | 1980-04-24 | 1982-07-01 | Beiersdorf Ag, 2000 Hamburg | Process for the production of impregnated smooth or creped papers in one operation on the paper machine and their use as carrier material for pressure-sensitive adhesive layers |
DE3202122A1 (en) * | 1982-01-23 | 1983-07-28 | Röhm GmbH, 6100 Darmstadt | METHOD FOR STRENGTHENING FIBERBUILDINGS BY MEANS OF AQUEOUS PLASTIC DISPERSIONS |
-
1985
- 1985-11-21 DE DE3541187A patent/DE3541187C2/en not_active Expired - Fee Related
-
1986
- 1986-07-30 AT AT86110511T patent/ATE59416T1/en not_active IP Right Cessation
- 1986-07-30 EP EP86110511A patent/EP0223922B2/en not_active Expired - Lifetime
- 1986-07-30 NO NO863075A patent/NO174725C/en unknown
- 1986-07-30 DE DE8686110511T patent/DE3676648D1/en not_active Expired - Lifetime
- 1986-08-04 FI FI863177A patent/FI86902C/en not_active IP Right Cessation
- 1986-08-06 PT PT83153A patent/PT83153B/en not_active IP Right Cessation
- 1986-08-08 DD DD86293532A patent/DD259885A5/en not_active IP Right Cessation
- 1986-08-12 ES ES8601027A patent/ES2000141A6/en not_active Expired
- 1986-11-17 CA CA000523131A patent/CA1329072C/en not_active Expired - Fee Related
- 1986-11-19 JP JP61274248A patent/JPH0726355B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52143117A (en) * | 1976-05-25 | 1977-11-29 | Tomoegawa Paper Co Ltd | Secondary original drawing paper |
JPS54120713A (en) * | 1978-03-06 | 1979-09-19 | Hoechst Gosei Kk | Treating agent and method for rendering paper transparent |
JPS5742994A (en) * | 1980-06-28 | 1982-03-10 | Letron Gmbh & Co | Production of synthetic substance coated plate |
Also Published As
Publication number | Publication date |
---|---|
EP0223922B1 (en) | 1990-12-27 |
NO863075D0 (en) | 1986-07-30 |
DE3541187C2 (en) | 1994-10-06 |
FI86902B (en) | 1992-07-15 |
DE3676648D1 (en) | 1991-02-07 |
DD259885A5 (en) | 1988-09-07 |
JPH0726355B2 (en) | 1995-03-22 |
FI863177A (en) | 1987-05-22 |
EP0223922B2 (en) | 1997-10-29 |
CA1329072C (en) | 1994-05-03 |
NO174725C (en) | 1994-06-22 |
NO174725B (en) | 1994-03-14 |
NO863075L (en) | 1987-05-22 |
PT83153A (en) | 1986-09-01 |
ATE59416T1 (en) | 1991-01-15 |
FI863177A0 (en) | 1986-08-04 |
FI86902C (en) | 1992-10-26 |
DE3541187C1 (en) | 1987-06-11 |
PT83153B (en) | 1988-07-29 |
EP0223922A1 (en) | 1987-06-03 |
ES2000141A6 (en) | 1987-12-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS62125097A (en) | Production of paper strip impregnated with synthetic resin in solution or dispersion form | |
US5215626A (en) | Process for applying a polysiloxane to tissue paper | |
EP0749509B1 (en) | Process for applying a thin film containing low levels of a functional-polysiloxane and a nonfunctional-polysiloxane to tissue paper | |
US7192653B2 (en) | Prepreg | |
JPH0376895A (en) | Manufacture of high compression paper including synthetic fiber and covering support material | |
CN105247137A (en) | Compositions and methods of making paper products | |
CN1330826C (en) | Pulp of paper for decoration use | |
CA2518942C (en) | Prepreg which is produced by impregnating a base paper with a combination of resin solution and polymer dispersion | |
US11619009B2 (en) | Prepeg with improved flatness | |
CA2234595A1 (en) | Single-side impregnated printing paper carriers | |
DE3015733A1 (en) | METHOD FOR PRODUCING IMPREGNATED SMOOTH OR CREEPED PAPER ON THE PAPER MACHINE | |
FI59441B (en) | SAETT FOER TILLVERKNING AV IMPREGNERAD OCH YTBEHANDLAD FOLIE | |
EP2314766B1 (en) | Printable glazed paper article and its production process | |
US20070009685A1 (en) | Support for image recording material | |
CA2523395A1 (en) | Wallpaper and method for production thereof | |
JP3776559B2 (en) | Manufacturing method of decorative sheet | |
JP2612441B2 (en) | Base paper for decorative sheet | |
JP3207131B2 (en) | Flexible paper | |
JPH07501362A (en) | Single-sided coated paper | |
DE10111115A1 (en) | Base paper with improved printability | |
JPS63190094A (en) | Pigment internally filled reinforcing paper | |
JPH046542B2 (en) | ||
MXPA96004010A (en) | Process for applying a thin film quecontains low levels of a polysylxoxfunctional and a non-functional polysylxoxan to papelhigien | |
JPH0814080B2 (en) | Reinforcement paper for decorative paper |