JPH01172613A - Roll for pressing - Google Patents
Roll for pressingInfo
- Publication number
- JPH01172613A JPH01172613A JP32876687A JP32876687A JPH01172613A JP H01172613 A JPH01172613 A JP H01172613A JP 32876687 A JP32876687 A JP 32876687A JP 32876687 A JP32876687 A JP 32876687A JP H01172613 A JPH01172613 A JP H01172613A
- Authority
- JP
- Japan
- Prior art keywords
- roll
- polyisocyanurate
- weight
- inorganic powder
- paper
- 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.)
- Pending
Links
- 238000003825 pressing Methods 0.000 title description 2
- 229920005989 resin Polymers 0.000 claims abstract description 24
- 239000011347 resin Substances 0.000 claims abstract description 24
- 239000000843 powder Substances 0.000 claims abstract description 23
- 229920000582 polyisocyanurate Polymers 0.000 claims abstract description 14
- 239000011495 polyisocyanurate Substances 0.000 claims abstract description 14
- 239000000463 material Substances 0.000 claims abstract description 12
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 10
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 10
- 125000003118 aryl group Chemical group 0.000 claims abstract description 8
- 238000005266 casting Methods 0.000 claims description 10
- 239000000945 filler Substances 0.000 claims description 2
- 238000004299 exfoliation Methods 0.000 abstract 2
- 229920001187 thermosetting polymer Polymers 0.000 abstract 2
- 238000000465 moulding Methods 0.000 abstract 1
- 239000000123 paper Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 9
- -1 Alkali metal salts Chemical class 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000010438 granite Substances 0.000 description 7
- 239000004575 stone Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 238000007788 roughening Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000004069 aziridinyl group Chemical group 0.000 description 2
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000013522 chelant Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000005829 trimerization reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- MFVFDTCSVFBOTL-UHFFFAOYSA-N 1,3-diazetidine Chemical compound C1NCN1 MFVFDTCSVFBOTL-UHFFFAOYSA-N 0.000 description 1
- NKFIBMOQAPEKNZ-UHFFFAOYSA-N 5-amino-1h-indole-2-carboxylic acid Chemical compound NC1=CC=C2NC(C(O)=O)=CC2=C1 NKFIBMOQAPEKNZ-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- 229920001875 Ebonite Polymers 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000005910 alkyl carbonate group Chemical group 0.000 description 1
- 150000004808 allyl alcohols Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 150000001913 cyanates Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical compound [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- ZUFQCVZBBNZMKD-UHFFFAOYSA-M potassium 2-ethylhexanoate Chemical compound [K+].CCCCC(CC)C([O-])=O ZUFQCVZBBNZMKD-UHFFFAOYSA-M 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- BWILYWWHXDGKQA-UHFFFAOYSA-M potassium propanoate Chemical compound [K+].CCC([O-])=O BWILYWWHXDGKQA-UHFFFAOYSA-M 0.000 description 1
- 235000010332 potassium propionate Nutrition 0.000 description 1
- 239000004331 potassium propionate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- JZWFDVDETGFGFC-UHFFFAOYSA-N salacetamide Chemical group CC(=O)NC(=O)C1=CC=CC=C1O JZWFDVDETGFGFC-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- NCTHNHPAQAVBEB-WGCWOXMQSA-M sodium ferulate Chemical compound [Na+].COC1=CC(\C=C\C([O-])=O)=CC=C1O NCTHNHPAQAVBEB-WGCWOXMQSA-M 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- NINIDFKCEFEMDL-OUBTZVSYSA-N sulfur-33 atom Chemical compound [33S] NINIDFKCEFEMDL-OUBTZVSYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Rolls And Other Rotary Bodies (AREA)
- Paper (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、特に天然石からなる製紙用トッププレスロー
ルの代替ロールとして好ましく用いられるプレス用ロー
ルに関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a press roll that is preferably used as an alternative roll to a papermaking top press roll made of natural stone.
に通過し、その際に押圧されて脱水される。フェルトに
接触するボトムプレス用ロールとしては、通常ゴムロー
ルが用られている。7ンナズグレスロールは、高い力t
−直接に湿紙に加えるため、次のような性能が要求され
る。The water passes through the water, where it is pressed and dehydrated. A rubber roll is usually used as the bottom press roll that comes into contact with the felt. 7 Nana's Gress roll has high power
-Since it is added directly to wet paper, the following performance is required.
(1)紙離れが良いこと。(1) Good separation from paper.
(2)高い荷量に耐える得ること。(2) Capable of withstanding high loads.
(3)表面が平滑であること。(3) The surface must be smooth.
(4)湿紙をプレスする時に変形がなく、紙が切断しな
いこと。(4) When pressing the wet paper, there should be no deformation and the paper should not be cut.
(5)耐ドクター性が良いこと。(5) Good doctor resistance.
(6) 自己発熱が少ないこと。(6) Low self-heating.
ストーンロールと称せられる花こう岩で作られたト、7
°プレスロールは、紙離れが良好であるが、材料が天然
物であるため材質のばらつきが大きく、ロールを成型す
る際に多くの労力と時間を要する。7 made of granite called stone roll
Press rolls have good paper release properties, but because they are made of natural materials, there are large variations in material quality, and it takes a lot of effort and time to form the rolls.
特に、大型のロールの製作納期が花こう岩の入手難によ
って不安定になる。また、ト、グプレスロールには、衝
撃によシ傷がつき易い欠点がある。In particular, the production deadline for large rolls becomes unstable due to the difficulty in obtaining granite. Additionally, press rolls have the disadvantage of being easily scratched by impact.
これに代わるものとして硬質がム中に珪砂のような石粉
を混入してなる製紙用ト、グデレス用ロールが知られて
いるが、このロールは強度が大きく、安価である利点を
有するが紙離れが不十分であり、使用中に石粉の脱落下
が促進されて表面に肌荒れが生じる欠点がある。このよ
うな欠点を解消するために特開昭50−90704号に
てエイキシ樹脂からなるプレス用ロール及びポリエステ
ル樹脂からなるプレス用ロールが開示されている。しか
し、これらのプレス用ロールは、無機質粉末との接着性
が悪い。As an alternative to this, there is known a roll for papermaking and for papermaking, which is made by mixing stone powder such as silica sand into a hard roll. There is a drawback that the stone powder is insufficiently removed, and the falling off of stone powder is promoted during use, causing roughness on the surface. In order to overcome these drawbacks, Japanese Patent Application Laid-Open No. 50-90704 discloses a press roll made of eixy resin and a press roll made of polyester resin. However, these press rolls have poor adhesion to inorganic powder.
また、6−ナイロン樹脂からなるプレス用ロールも開示
されているが、エポキシ樹脂からなるプレス用ロールの
欠点に加えて耐熱性が悪す欠点を有する。更に、ポリウ
レタン樹脂からなるプレス用ロールが特開昭57−95
395号にて開示されているが、このロールの場合も、
成型性が悪い欠点を有している。A press roll made of 6-nylon resin has also been disclosed, but in addition to the drawbacks of a press roll made of epoxy resin, it has the disadvantage of poor heat resistance. Furthermore, a press roll made of polyurethane resin was published in JP-A-57-95.
Although it is disclosed in No. 395, in the case of this roll as well,
It has the disadvantage of poor moldability.
熱性に優れ無機質粉末の脱落によるロール表面の肌荒れ
が極めて少なく、シかも、成型性の良いプレス用ロール
を提供するものである。The present invention provides a press roll that has excellent heat resistance, has extremely little roughening of the roll surface due to shedding of inorganic powder, and has good moldability.
本発明は、ポリイソシアネート基含有率20重量−以上
の芳香族ポリイソシアネートを50重量−以上含有して
なるポリイソシアヌレート樹脂形成用注型材を注盤した
後加熱効果させたショアD硬度が75以上の非多孔質ポ
リイソシアヌレート系樹脂層に無機質粉末を含有したも
のを芯体の表面に設けてなることを特徴とするプレス用
ロールである。The present invention provides a casting material for forming polyisocyanurate resin containing 50 weight or more of aromatic polyisocyanate with a polyisocyanate group content of 20 weight or more. This is a press roll characterized in that a non-porous polyisocyanurate resin layer containing inorganic powder is provided on the surface of a core.
ここで、プリイソシアヌレート系樹脂は、イリイソシア
ヌレート系樹脂100重量優に対して5〜800重量−
の充填剤を含有させることが好ましい。Here, the amount of preisocyanurate resin is 5 to 800% by weight per 100% by weight of irisocyanurate resin.
It is preferable to contain a filler of.
また、イソシアネート基含有率20重量%以上の芳香族
?ジイソシアネートとは、例えば、トリレン−2,4−
または−2,6−ジインシアネート、ジフェニルメタン
−2,4′−またFi−4,4’−ジイソシアネート、
ナフチレン−1,5−ジイソシアネート、eトリレンジ
イソシアネート、アニシソンジイソシアネート、ジフェ
ニルエーテル−4,4′−ジイソシアネート、m−また
#″ipip−フエニレンソイソシアネートフェニルメ
タン−4# 4’t 4’−トリインシアネート、トリ
ス(4−インシアナトフェニル)チオホスフェート、ア
ニリンをホルマリンと縮合してからホスゲン化して得ら
れる種類のポリフェニルポリメチレンプリイソシアネー
ト、ドイツ特許1092007に記載されているような
カルゲノイミド基またはウレトンイミン基をもつ常温で
液状のジフェニルメタンジイソシアネート類、あるいは
、インシアネート基含有率が20重量%以上のウレタン
結合、アロファネート結合、アミド結合、ウレア結合、
アシルウレア結合、ビウレ、ト結合、インシアヌレート
猿構造、ウレチジンジオン猿構造などを含有する改質芳
香族ポリイソシアネート類などがあげられる。Also, aromatic compounds with an isocyanate group content of 20% by weight or more? Diisocyanate is, for example, tolylene-2,4-
or -2,6-diisocyanate, diphenylmethane-2,4'-also Fi-4,4'-diisocyanate,
naphthylene-1,5-diisocyanate, e-tolylene diisocyanate, anisone diisocyanate, diphenyl ether-4,4'-diisocyanate, m-Also#"ipip-phenylene soocyanate phenylmethane-4# 4't 4'-triyne cyanates, tris(4-incyanatophenyl)thiophosphate, polyphenylpolymethylene preisocyanates of the type obtained by condensation of aniline with formalin and subsequent phosgenation, cargenoimide groups or uretonimine groups as described in German Patent No. 1092007; diphenylmethane diisocyanates that are liquid at room temperature, or urethane bonds, allophanate bonds, amide bonds, urea bonds with an incyanate group content of 20% by weight or more,
Examples include modified aromatic polyisocyanates containing acylurea bonds, biurea bonds, to bonds, incyanurate structures, uretidine dione structures, and the like.
芳香族−ジイソシアネートは、1種または2種以上の混
合物としても使用できる。これらの中商業的に容易に入
手できる芳香族プリイソシアネート類、例えば、トリレ
ン−2,4−ジイソシアネートおよびトリレン−2,6
−ジイソシアネートおよびこれら異性体のあらゆる混合
物、アニリンをホルマリンと縮合してからホスゲン化し
て得られる種類の一すフェニルポリメチレンポリイソシ
アネニト類、ジフェニルメタン−4,4′−ゾイソシア
ネートおよびジフェニルメタン−2,4′−ジイソシア
ネートおよびこれら異性体のあらゆる混合物、イソシア
ネート基含有率が20重量%以上の液状化ジフェニルメ
タンジイソシアネート類などが特に好適である。Aromatic diisocyanates can also be used singly or as a mixture of two or more. Among these are commercially readily available aromatic preisocyanates, such as tolylene-2,4-diisocyanate and tolylene-2,6-diisocyanate.
- diisocyanates and all mixtures of these isomers, monophenylpolymethylene polyisocyanenites of the type obtained by condensation of aniline with formalin and subsequent phosgenation, diphenylmethane-4,4'-zoisocyanate and diphenylmethane-2,4 '-Diisocyanates and all mixtures of these isomers, liquefied diphenylmethane diisocyanates with an isocyanate group content of 20% by weight or more are particularly suitable.
ポリイソシアヌレート樹脂形成用注型材とは、芳香族プ
リイソシアネートを50重量−以上を含有し、三量化触
媒と、必要に応じて芳香族ポリイソシアネートに可溶で
同時重合可能な樹脂及び単量体等を含むものである。A casting material for forming a polyisocyanurate resin is a material containing 50% by weight or more of an aromatic preisocyanate, a trimerization catalyst, and optionally a resin and monomer that are soluble in the aromatic polyisocyanate and can be copolymerized. etc.
三量化触媒としては、公知のものが使用でき、例えば、
炭素数が2〜12カルゲン酸のアルカリ金属塩(酢酸カ
リウム、プロピオン酸カリウム、2−エチルへキサン酸
カリウム、安息香酸ナトリウム等)、炭素数が13以上
のカルボン酸のアルカリ金属塩(オレイン酸ナトリウム
、リルン酸カリウム等)、ナトリウムフェルレートのよ
うなカルボン酸以外の弱酸のアルカリ金属塩などの塩基
性物質、ナトリウムメトキシド、ベンジルトリメチルア
ンモニウムヒドロキシド、アルカリ金属尿酸化物などの
強塩基性物質、サリチルアルデヒドとカリウムのキレー
ト化合物で代表されるキレート化合物、ナフテン酸カル
シウム、ナフテン酸鉛、カプリル酸鉛などのカルボン酸
のアルカリ金属以外の金属塩、特願昭58−12671
号に記載されているようなアジリジニル化合物および三
級アミン類および/lたはアジリジニル化合物と助触媒
(フェノール類、エポキシ化合物、アルキルカーボ′ネ
ート類など)の組合せなどである。以上の触媒は、単独
または混合物としても使用できる。触媒の配合率は、注
型材のポットライ7や触媒の強さによって適宜、決定さ
れるものであるが、注型材中に通常0.1〜10%重量
−程度含有せしめるようにする。As the trimerization catalyst, known ones can be used, for example,
Alkali metal salts of carboxylic acids with 2 to 12 carbon atoms (potassium acetate, potassium propionate, potassium 2-ethylhexanoate, sodium benzoate, etc.), alkali metal salts of carboxylic acids with 13 or more carbon atoms (sodium oleate, etc.) , potassium lylphate, etc.), basic substances such as alkali metal salts of weak acids other than carboxylic acids such as sodium ferulate, strong basic substances such as sodium methoxide, benzyltrimethylammonium hydroxide, alkali metal urinary oxides, salicyl Chelate compounds represented by aldehyde and potassium chelate compounds, non-alkali metal salts of carboxylic acids such as calcium naphthenate, lead naphthenate, lead caprylate, etc., patent application No. 12671/1986
Examples include combinations of aziridinyl compounds and tertiary amines and/or aziridinyl compounds and cocatalysts (phenols, epoxy compounds, alkyl carbonates, etc.) as described in No. The above catalysts can be used alone or as a mixture. The blending ratio of the catalyst is appropriately determined depending on the pot lie 7 of the casting material and the strength of the catalyst, but it is usually contained in the casting material in an amount of about 0.1 to 10% by weight.
同時重合可能な樹脂としては、例えば活性水素含有樹脂
(ヒドロキシル基含有樹脂やアミン基含有樹脂で例えば
、ポリエーテルポリオール、ポリエーテルポリオール、
−リカー?ネート?リオール、炭化水素系長鎖4リオー
ル、ポリエーテルポリアミン等)、不飽和ポリエステル
樹脂、ジアリルフタレート樹脂、エポキシ樹脂などであ
る。また、同時重合可能な単量体としてはエチレン性不
飽和結合金有化合物(例えば、スチレン、?ニルスチレ
ン、アクリル酸エステル類、メタクリル酸エステル類、
アリルアルコールエステル化物ナト)を例示できる。Copolymerizable resins include, for example, active hydrogen-containing resins (hydroxyl group-containing resins and amine group-containing resins such as polyether polyols, polyether polyols,
-Liquor? Nate? polyol, hydrocarbon long-chain 4-liol, polyether polyamine, etc.), unsaturated polyester resin, diallyl phthalate resin, epoxy resin, etc. In addition, copolymerizable monomers include ethylenically unsaturated bond-bearing compounds (for example, styrene, ?nylstyrene, acrylic esters, methacrylic esters,
Examples include allyl alcohol esters.
また、芯体上に硬質のポリイソシアスレート系樹脂層を
形成する方法としては、例えば注型法、即ち、全屋内は
所定間隔を保持して芯体を設置した後、硬質ポリインシ
アヌレート系樹脂原料を注入し、硬化させる方法がある
。In addition, as a method for forming a hard polyisocyanurate resin layer on the core, for example, a casting method is used. There is a method of injecting raw materials and curing them.
また、無機質粉末としては、花こう岩、珪砂、長石等の
石粉を包含する。石粉は、5102、または5102と
Az2o3を主成分として含有する。また、CaF2、
CaO、MgO、At203、Boo、ZnO1Ti0
2、S 102.5n02、Cu2O、Na2S、 1
202、CabSCub、ZnS、 Pb8゜pbz2
.5b2s5、B1253、A128%81C%Cu2
S、 5nS2、HgS、 CuI、AgI等をそれぞ
れ主成分とする粉体もその表面の性質を利用して使用可
能である。無機質粉末の性質に従い、ロール表面を親水
性にしたい場合は親水性粉体を使用し、また逆に疎水性
にしfc−場合は疎水性粉体を用いる。また、親水性、
疎水性の粉体を混合することによシ、その混合比によっ
てロール表面の性質を変えることが可能である。Inorganic powders include stone powders such as granite, silica sand, and feldspar. The stone powder contains 5102 or 5102 and Az2o3 as main components. In addition, CaF2,
CaO, MgO, At203, Boo, ZnO1Ti0
2, S 102.5n02, Cu2O, Na2S, 1
202, CabSCub, ZnS, Pb8゜pbz2
.. 5b2s5, B1253, A128%81C%Cu2
Powders containing S, 5nS2, HgS, CuI, AgI, etc. as main components can also be used by taking advantage of their surface properties. Depending on the properties of the inorganic powder, if the roll surface is to be made hydrophilic, a hydrophilic powder is used, and if the roll surface is to be made hydrophobic, a hydrophobic powder is used. Also, hydrophilic,
By mixing hydrophobic powders, it is possible to change the properties of the roll surface depending on the mixing ratio.
本発明のプレス用ロールは、好ましくはその中心を貫通
し、ロールに結合する鉄棒のような芯体を具備している
。この芯体は必ずしもロールの中心を貫通する必要はな
く、適切な固定具によってロールの両端面に固定しても
よい。The press roll of the present invention preferably includes a core such as an iron rod that passes through the center and is coupled to the roll. This core does not necessarily have to pass through the center of the roll, but may be fixed to both end faces of the roll by suitable fasteners.
本発明にかかるプレス用ロールによれば、ポリイソシア
ネート基含有率20重量−以上の芳香族ポリイソシアネ
ートを50重量%以上含有してなるポリイソシアヌレー
ト樹脂形成用注型材を注型し九後加熱効果させたショア
D硬度が75以上で無機質粉末を含有した非多孔質ポリ
イソシアヌレート系樹脂層を芯体の表面に設けているの
で、紙との剥離性が優れ、物理的強度が強く、耐熱性優
れ無機質粉末の脱落によるロール表面の肌荒れが極めて
少なく良好な成型性を発揮することができるものである
。According to the press roll according to the present invention, the casting material for forming a polyisocyanurate resin containing 50% by weight or more of an aromatic polyisocyanate with a polyisocyanate group content of 20% by weight or more is cast, and the heating effect is obtained after the casting. A non-porous polyisocyanurate resin layer containing inorganic powder with a Shore D hardness of 75 or more is provided on the surface of the core, so it has excellent peelability from paper, strong physical strength, and heat resistance. Excellent: There is very little roughening of the roll surface due to shedding of the inorganic powder, and good moldability can be exhibited.
以下、本発明の実施例について説明する。 Examples of the present invention will be described below.
表面をプラスト処理して芯金を貫通させた注型用モール
ドを用意する。ジ7工二ルメタンー4.4/−ソイソシ
アネート100重量部に、デスモフェン2020(バイ
エル社製ポリへキサメチレンカーボネートジオール、水
酸基価56.2)を10重量部、60℃で溶融混合した
。この混和物に乾燥保温された硼砂粉末150重量部を
添加し、減圧下で攪拌する。この混合物に0.5重量部
のN、N’、N’) !Jス(ジメチルアミノプロピル
)ヘキサヒドロ−8−)リアジンを加え激しく攪拌混合
後減圧デシケーター中にて5mHg以下で1分間脱泡し
た。このものを70℃に加熱した上記注型用モールドに
注入し、これを140℃で2時間及び180℃で4時間
硬化した。140℃に冷却してから、生成した硬化物を
上記モールドより取り出し常法によシ表面研暦全行ない
実施例のロールを得た。Prepare a casting mold whose surface is treated with plastic and has a core passed through it. 10 parts by weight of Desmophene 2020 (polyhexamethylene carbonate diol manufactured by Bayer, hydroxyl value 56.2) was melt-mixed at 60°C to 100 parts by weight of di7-dylmethane-4.4/-isoisocyanate. 150 parts by weight of dry and kept borax powder is added to this mixture, and the mixture is stirred under reduced pressure. Add 0.5 parts by weight of N, N', N') to this mixture! Js(dimethylaminopropyl)hexahydro-8-)riazine was added and mixed with vigorous stirring, followed by defoaming for 1 minute at 5 mHg or less in a vacuum desiccator. This material was poured into the casting mold heated to 70°C, and cured at 140°C for 2 hours and at 180°C for 4 hours. After cooling to 140° C., the resulting cured product was taken out from the mold and subjected to surface polishing in a conventional manner to obtain a roll as an example.
比較例
下記組成物を常法に従いオープンミルで混練りし、キャ
レンダーロールを用いてコ9ムシートニ形成する。この
ゴムシートを表面にエボナイト層が形成された鉄芯に巻
き付け、ラッピングクロスで締め付けて加硫し、最後に
表面研磨を実施して比較例のロールを得た。COMPARATIVE EXAMPLE The following composition was kneaded in an open mill according to a conventional method, and then formed into a sheet using a calender roll. This rubber sheet was wrapped around an iron core with an ebonite layer formed on the surface, tightened with a wrapping cloth and vulcanized, and finally the surface was polished to obtain a roll of a comparative example.
組成 重量部
天然ゴム 100
亜鉛華 5
微粉イオウ 33
加硫促進剤 0.6エビナイト粉末
80
硅砂粉末 150
実施例および比較例のロールを花こう岩から成るロール
と共に長網式抄紙機でテストした。テストに際しては、
実施例のロール、比較例のロールおよび花こう岩のロー
ルは、下記衣の条件で制御される。抄紙される・臂ルグ
は広葉樹クラフトパルプ100チから成るものであって
、10重量%のサイズ剤を含有し、そして硫酸バンドで
pH4,5に調整されている。7リーネスは450d、
秤、tけ8077m である。Composition Parts by Weight Natural Rubber 100 Zinc White 5 Fine Sulfur 33 Vulcanization Accelerator 0.6 Evinite Powder 80 Silica Sand Powder 150 The rolls of Examples and Comparative Examples were tested on a Fourdrinier paper machine together with rolls made of granite. When testing,
The example roll, the comparative example roll, and the granite roll were controlled under the following coating conditions. The pulp from which the paper is made consists of 100 ml of hardwood kraft pulp, contains 10% by weight of sizing agent, and is adjusted to pH 4.5 with sulfuric acid. 7 Leeness is 450d,
The scale weighs 8077m.
実施例ロール、比較例ロールおよび花こう岩は30胴の
鉄芯径、60簡の外径% 260目の長さを有してい
る。The example roll, comparative example roll, and granite have an iron core diameter of 30 mm, an outer diameter% of 60 mm, and a length of 260 mm.
ステンレス製のドクターナイフを試験ロールに接続させ
て10分間抄紙′に実施した。その結果、本発明の実施
例ロールは、ドクターナイフによる傷付きが少なく、紙
のはく離性が良好であり、紙かすの付着量が比較例ロー
ルに比べ少なく、花こう岩ロールと同等の性能を有した
。ま念ロールの耐圧性に関しても問題がなかった。A stainless steel doctor knife was connected to the test roll and the paper was made for 10 minutes. As a result, the example roll of the present invention was less scratched by a doctor knife, had good paper releasability, had less paper residue than the comparative example roll, and had the same performance as the granite roll. I had it. There were no problems with the pressure resistance of the Manen roll.
また本発明のプレス用ロールは製紙用ブレスロールとし
て好ましく用いられるが、これに限定されずその他にも
裏紙用カレンダーロール、グロスカレンダーロール、プ
レイカースタックロール、スムーfロール、磁気テーフ
用カレンダーロール、布のエンボスロール、乾式複写機
の圧定着用ロール等にも用いられる。Further, the press roll of the present invention is preferably used as a press roll for papermaking, but is not limited to this, and can also be used as a calendar roll for backing paper, a gloss calendar roll, a play car stack roll, a smooth f roll, and a calendar roll for magnetic tape. It is also used for fabric embossing rolls, pressure fixing rolls for dry copying machines, etc.
以上説明した如く、本発明にかかるプレス用ロールによ
れば、紙との剥離性が優n1物狸的強度が強く、耐熱性
優れ無機質粉末の脱落によるロール表面の肌荒れが極め
て少なく良好な成型性を発揮することができるものであ
る。As explained above, the press roll according to the present invention has excellent peelability from paper, excellent strength, excellent heat resistance, and very little roughening of the roll surface due to shedding of inorganic powder, and good moldability. It is possible to demonstrate the
Claims (2)
香族ポリイソシアネートを50重量%以上含有してなる
ポリイソシアヌレート樹脂形成用注型材を注型した後加
熱硬化させたショアD硬度が75以上の非多孔質ポリイ
ソシアヌレート系樹脂層に無機質粉末を含有したものを
芯体の表面に設けてなることを特徴とするプレス用ロー
ル。(1) A casting material for forming a polyisocyanurate resin containing 50% by weight or more of an aromatic polyisocyanate with a polyisocyanate group content of 20% by weight or more has a Shore D hardness of 75 or more after being heated and cured. A press roll comprising a non-porous polyisocyanurate resin layer containing inorganic powder on the surface of a core.
レート系樹脂100重量%に対して5〜800重量%の
充填剤を含有したものであることを特徴とする特許請求
の範囲第1項記載のプレス用ロール。(2) The press according to claim 1, wherein the polyisocyanurate resin contains 5 to 800% by weight of filler based on 100% by weight of the polyisocyanurate resin. Roll for use.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32876687A JPH01172613A (en) | 1987-12-25 | 1987-12-25 | Roll for pressing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32876687A JPH01172613A (en) | 1987-12-25 | 1987-12-25 | Roll for pressing |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01172613A true JPH01172613A (en) | 1989-07-07 |
Family
ID=18213902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32876687A Pending JPH01172613A (en) | 1987-12-25 | 1987-12-25 | Roll for pressing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01172613A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61112612A (en) * | 1984-11-07 | 1986-05-30 | Nippon Polyurethan Kogyo Kk | Manufacture of resin roll |
-
1987
- 1987-12-25 JP JP32876687A patent/JPH01172613A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61112612A (en) * | 1984-11-07 | 1986-05-30 | Nippon Polyurethan Kogyo Kk | Manufacture of resin roll |
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