JPH0483100A - Bolt fixing cartridge excellent in light resistance - Google Patents
Bolt fixing cartridge excellent in light resistanceInfo
- Publication number
- JPH0483100A JPH0483100A JP19618290A JP19618290A JPH0483100A JP H0483100 A JPH0483100 A JP H0483100A JP 19618290 A JP19618290 A JP 19618290A JP 19618290 A JP19618290 A JP 19618290A JP H0483100 A JPH0483100 A JP H0483100A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- bolt fixing
- light resistance
- thermosetting resin
- container
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 31
- 239000011347 resin Substances 0.000 claims abstract description 31
- 239000003086 colorant Substances 0.000 claims abstract description 12
- 229920001187 thermosetting polymer Polymers 0.000 claims abstract description 10
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 239000011521 glass Substances 0.000 abstract description 12
- 239000000203 mixture Substances 0.000 abstract description 6
- 239000000049 pigment Substances 0.000 abstract description 4
- 229920006337 unsaturated polyester resin Polymers 0.000 abstract description 4
- 239000000178 monomer Substances 0.000 abstract description 3
- 239000004342 Benzoyl peroxide Substances 0.000 abstract description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract description 2
- 239000003112 inhibitor Substances 0.000 abstract description 2
- 150000001451 organic peroxides Chemical class 0.000 abstract description 2
- 238000006116 polymerization reaction Methods 0.000 abstract description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 2
- 229960003328 benzoyl peroxide Drugs 0.000 abstract 1
- 230000000593 degrading effect Effects 0.000 abstract 1
- 230000009257 reactivity Effects 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- FSJSYDFBTIVUFD-SUKNRPLKSA-N (z)-4-hydroxypent-3-en-2-one;oxovanadium Chemical compound [V]=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FSJSYDFBTIVUFD-SUKNRPLKSA-N 0.000 description 1
- MMEDJBFVJUFIDD-UHFFFAOYSA-N 2-[2-(carboxymethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC=C1CC(O)=O MMEDJBFVJUFIDD-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002969 artificial stone Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- LZKLAOYSENRNKR-LNTINUHCSA-N iron;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Fe].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O LZKLAOYSENRNKR-LNTINUHCSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- SGGOJYZMTYGPCH-UHFFFAOYSA-L manganese(2+);naphthalene-2-carboxylate Chemical compound [Mn+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 SGGOJYZMTYGPCH-UHFFFAOYSA-L 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- GYVGXEWAOAAJEU-UHFFFAOYSA-N n,n,4-trimethylaniline Chemical compound CN(C)C1=CC=C(C)C=C1 GYVGXEWAOAAJEU-UHFFFAOYSA-N 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
Landscapes
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、コンクリート、岩盤等(以下、母材という)
に、アンカーボルトを固着するためのボルト固定用カー
トリッジに関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention is applicable to concrete, rock, etc. (hereinafter referred to as base material).
The present invention relates to a bolt fixing cartridge for fixing an anchor bolt.
従来、アンカーボルトの固着方法として母材に穿孔し、
その孔内にカプセルを装填しハンマードリル等に接合し
たアンカーに回転・打撃を与えながらアンカーボルトを
孔内に挿入し、容器を破砕し容器に収容された不飽和ポ
リエステル樹脂等の熱硬化性樹脂を硬化させ、アンカー
ボルトを固着する方法が知られている(特公昭38−1
2863号公報)。Conventionally, the method of fixing anchor bolts was to drill holes in the base material.
A capsule is loaded into the hole, and an anchor bolt connected to a hammer drill etc. is rotated and struck into the hole, and the anchor bolt is inserted into the hole to crush the container and thermosetting resin such as unsaturated polyester resin contained in the container. A method of hardening anchor bolts and fixing them is known (Special Publication No. 38-1).
2863).
これらの固着剤に用いられる熱硬化性樹脂は、ラジカル
反応により 硬化させるタイプのものが殆どであった。Most of the thermosetting resins used in these adhesives were of the type that hardened through radical reactions.
該樹脂は、常温で硬化する様設計されているため、アン
カー施工の作業性は優れていた。反面、太陽光線中の、
可視光線及び紫外線に非常に敏感であり反応性に富んで
いた。容器が無色ガラス管では350mm以上の波長の
光はほとんど透過し、該樹脂は短時間でゲル化するため
、着色ガラス管に収容されていた。Since the resin was designed to harden at room temperature, the workability of anchor construction was excellent. On the other hand, in the sunlight,
It was highly sensitive and reactive to visible and ultraviolet light. If the container was a colorless glass tube, most of the light with a wavelength of 350 mm or more would pass through, and the resin would gel in a short time, so it was housed in a colored glass tube.
樹脂を保護するためだけの着色ガラス管であれば、真黒
のガラスにすることにより問題は解決できる。しかし、
真黒のガラスでは収容された樹脂の流動性をチエツクす
ることができない(ボルト固定用カートリッジの性能チ
エツクで樹脂の流動性チエツクは必須である。)。If the colored glass tube is used only to protect the resin, the problem can be solved by using jet black glass. but,
With jet black glass, it is not possible to check the fluidity of the contained resin (checking the fluidity of the resin is essential when checking the performance of bolt-fixing cartridges).
また、褐色ガラスでは350nmで90%、450nm
で80%、550nmで40%程度の吸収である。従っ
て、着色ガラスを使用しても樹脂の保存性を向上させる
ことはできない。In addition, for brown glass, 90% at 350nm and 450nm
The absorption is about 80% at 550 nm, and about 40% at 550 nm. Therefore, even if colored glass is used, the storage stability of the resin cannot be improved.
本発明の目的は、固着剤としての性能を低下させること
なく、太陽光線中の可視光線及び紫外線に長時間耐え得
るボルト固定用カートリッジを提供することにある。An object of the present invention is to provide a cartridge for bolt fixing that can withstand visible light and ultraviolet rays in sunlight for a long time without deteriorating its performance as a fixing agent.
即ち、本発明は、破砕可能な容器に熱硬化性樹脂を収容
し、該樹脂とは分離した硬化剤とからなるボルト固定用
カートリッジにおいて、前記樹脂に樹脂と反応しない着
色剤を含むことを特徴とするボルト固定用カートリッジ
である。That is, the present invention provides a cartridge for bolt fixing that contains a thermosetting resin in a crushable container and a curing agent that is separated from the resin, and is characterized in that the resin contains a coloring agent that does not react with the resin. This is a cartridge for bolt fixing.
本発明に用いる容器は、施工時ドリルに取りつけられた
アンカーボルト等の回転・打撃挿入運動で簡単に破砕さ
れるものであれば特に限定されないが、例えば、ガラス
、陶器、磁器、合成樹脂、紙等が挙げられる。The container used in the present invention is not particularly limited as long as it can be easily crushed by the rotation or impact insertion movement of an anchor bolt attached to a drill during construction, but examples include glass, ceramics, porcelain, synthetic resin, and paper. etc.
本発明に用いる熱硬化性樹脂は、常温で容易に硬化させ
ることができるもので、例えば、不飽和ポリエステル樹
脂、ビニルエステル樹脂、エポキシアクリレート樹脂等
にスチレンモノマー、メタクリル酸メチル等の反応性単
量体を混合した物である。The thermosetting resin used in the present invention can be easily cured at room temperature, and includes, for example, unsaturated polyester resin, vinyl ester resin, epoxy acrylate resin, etc., and reactive monomers such as styrene monomer and methyl methacrylate. It is a mixture of bodies.
本発明に用いる硬化剤は、有機過酸化物、例えば、ベン
ゾイルパーオキサイド、メチルエチルケトンパーオキサ
イド、アセチルパーオキサイド等である。また、樹脂の
硬化を促進するための硬化促進剤を前記熱硬化性樹脂に
添加することができる。使用される硬化促進剤は、例え
ば、ジメチルアニリン、ジエチルアニリン、ジメチルパ
ラトルイジン等のアミン類、ナフテン酸コバルト、オク
トエ酸コバルト、ナフテン酸マンガン等の金属石鹸類、
バナジルアセチルアセトネート、鉄アセチルアセトネー
ト等のキレート化合物である。さらに、樹脂の安定性を
維持するためのハイドロキノン、ナフトキノン等の重合
禁止剤を加えることもできる。また、必要に応じて、砕
石、大理石等の天然砕石、または、マグネシャクリンカ
−等の人工石等の骨材を使用することもできる。The curing agent used in the present invention is an organic peroxide such as benzoyl peroxide, methyl ethyl ketone peroxide, acetyl peroxide, and the like. Further, a curing accelerator for accelerating curing of the resin can be added to the thermosetting resin. Examples of hardening accelerators used include amines such as dimethylaniline, diethylaniline, and dimethylparatoluidine; metal soaps such as cobalt naphthenate, cobalt octoate, and manganese naphthenate;
These are chelate compounds such as vanadyl acetylacetonate and iron acetylacetonate. Furthermore, a polymerization inhibitor such as hydroquinone or naphthoquinone can be added to maintain the stability of the resin. Further, if necessary, aggregates such as crushed stone, natural crushed stone such as marble, or artificial stone such as magnesha clinker can also be used.
本発明の特徴である前記樹脂とは反応しない着色剤は、
樹脂に含有されている反応性単量体に溶解し着色するも
のあるいは、実質的に均一に分散し長期保存で分解しな
いものであり、レーキ顔料、アゾ顔料、フタロシアニン
顔料、高級有機顔料及び無機顔料、その単品及びそれら
の混合物である。The coloring agent that does not react with the resin, which is a feature of the present invention, is
Those that dissolve and color the reactive monomers contained in the resin, or those that are substantially uniformly dispersed and do not decompose during long-term storage, such as lake pigments, azo pigments, phthalocyanine pigments, high-grade organic pigments, and inorganic pigments. , single items and mixtures thereof.
例えば、トーナーイエロー、トーナーブラウン、トーナ
ーグリーン〔武田薬品■製〕、カラーテックスブラウン
、カラーテックスオレンジ、カラーテックスマロン〔山
陽色素■製〕及びオプラスエロー〔オリエント化学■製
〕等の商品名で販売されているものが挙げられるが、そ
れらに限定されるものではない。For example, it is sold under product names such as Toner Yellow, Toner Brown, Toner Green [manufactured by Takeda Pharmaceutical ■], Colortex Brown, Colortex Orange, Colortex Maron [manufactured by Sanyo Shiki ■], and Oplus Yellow [manufactured by Orient Chemical ■]. Examples include, but are not limited to, those that exist.
本発明のボルト固定用カートリッジの配合組成は、主成
分である熱硬化性樹脂100重量に対して、着色剤0.
05〜2.0重量部、硬化促進剤0.05〜5重量部、
硬化剤1.0〜20重量部の範囲が好ましい。The composition of the bolt fixing cartridge of the present invention is as follows: 0.00% colorant per 100% weight of thermosetting resin, which is the main component.
05-2.0 parts by weight, curing accelerator 0.05-5 parts by weight,
A range of 1.0 to 20 parts by weight of the curing agent is preferred.
また、必要に応じて上記着色剤を2種類以上混合して使
用することもできる。Furthermore, two or more of the above coloring agents may be used in combination, if necessary.
以下、実施例により本発明の詳細な説明する。 Hereinafter, the present invention will be explained in detail with reference to Examples.
実施例1
外径13肛、肉厚0.6mm、長さ100■の無色ガラ
ス管及び褐色ガラス管に不飽和ポリエステル樹脂100
重量部、ジメチルアニリン1.0重量部、ノ1イドロキ
ノン0.2重量部、着色剤〔オリエント化学銖)製、オ
ブラスエロー#130) 0.1重量部を添加した混合
物5gを充填し容器を溶封した。次に このカートリッ
ジをガラス管立てに入れて直射日光下に置き、暴露試験
を行った。樹脂の流動性が無くなった時間(ゲル化時間
)を観察した。その結果を第1表に示す。Example 1 A colorless glass tube and a brown glass tube with an outer diameter of 13 mm, a wall thickness of 0.6 mm, and a length of 100 mm were coated with unsaturated polyester resin 100 mm.
The container was filled with 5 g of a mixture containing 1.0 parts by weight of dimethylaniline, 0.2 parts by weight of monohydroquinone, and 0.1 parts by weight of a coloring agent (manufactured by Orient Chemical Co., Ltd., Obras Yellow #130), and the container was melt-sealed. did. Next, this cartridge was placed in a glass tube stand and placed under direct sunlight for an exposure test. The time required for the resin to lose its fluidity (gelling time) was observed. The results are shown in Table 1.
実施例2
実施例1で用いた着色剤を、トーナーグリーン〔武田薬
品■製、商品名〕に代える以外は、実施例1と同様にカ
ートリッジを調製し、暴露試験を行った。その結果を第
1表に示す。Example 2 A cartridge was prepared in the same manner as in Example 1, except that the colorant used in Example 1 was replaced with Toner Green (manufactured by Takeda Pharmaceutical Co., Ltd., trade name), and an exposure test was conducted. The results are shown in Table 1.
実施例3
実施例1で用いた着色剤を、カーラ−テックス〔山陽色
素■製、商品名〕に代える以外は、実施例1と同様にカ
ートリッジを調製し、暴露試験を行った。その結果を第
1表に示す。Example 3 A cartridge was prepared in the same manner as in Example 1, except that the colorant used in Example 1 was replaced with Curlertex (manufactured by Sanyo Shiki ■, trade name), and an exposure test was conducted. The results are shown in Table 1.
比較例1
着色剤を用いない以外は、実施例1と同様にカートリッ
ジを調製し、暴露試験を行った。その結果を第1表に示
す。Comparative Example 1 A cartridge was prepared in the same manner as in Example 1, except that no colorant was used, and an exposure test was conducted. The results are shown in Table 1.
第1表
〔発明の効果〕
本発明のボルト固定用カートリッジは、着色剤を添加す
ることにより著しく耐光性を向上させ、製品の安定性が
得られた。Table 1 [Effects of the Invention] The bolt fixing cartridge of the present invention had significantly improved light resistance by adding a colorant, and the stability of the product was obtained.
特許出願人 旭化成工業株式会社Patent applicant: Asahi Kasei Industries, Ltd.
Claims (1)
は分離した硬化剤とからなるボルト固定用カートリッジ
において、前記樹脂に樹脂とは反応しない着色剤を含む
ことを特徴とするボルト固定用カートリッジ。1. A bolt fixing cartridge comprising a thermosetting resin contained in a crushable container and a curing agent separated from the resin, the bolt characterized in that the resin contains a coloring agent that does not react with the resin. Fixed cartridge.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2196182A JPH0678719B2 (en) | 1990-07-26 | 1990-07-26 | Bolt fixing cartridge with excellent light resistance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2196182A JPH0678719B2 (en) | 1990-07-26 | 1990-07-26 | Bolt fixing cartridge with excellent light resistance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0483100A true JPH0483100A (en) | 1992-03-17 |
JPH0678719B2 JPH0678719B2 (en) | 1994-10-05 |
Family
ID=16353566
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2196182A Expired - Lifetime JPH0678719B2 (en) | 1990-07-26 | 1990-07-26 | Bolt fixing cartridge with excellent light resistance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0678719B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5901383A (en) * | 1993-12-27 | 1999-05-11 | Toto Ltd. | Support structure for a toilet cover unit |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55111600A (en) * | 1979-02-19 | 1980-08-28 | Nippon Oils & Fats Co Ltd | Fixing agent cartridge |
JPS5722356A (en) * | 1980-07-15 | 1982-02-05 | Ouken Seikou Kk | Manufacture of coil |
-
1990
- 1990-07-26 JP JP2196182A patent/JPH0678719B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55111600A (en) * | 1979-02-19 | 1980-08-28 | Nippon Oils & Fats Co Ltd | Fixing agent cartridge |
JPS5722356A (en) * | 1980-07-15 | 1982-02-05 | Ouken Seikou Kk | Manufacture of coil |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5901383A (en) * | 1993-12-27 | 1999-05-11 | Toto Ltd. | Support structure for a toilet cover unit |
Also Published As
Publication number | Publication date |
---|---|
JPH0678719B2 (en) | 1994-10-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1075067A (en) | Photopolymerizable composition containing an ester, benzoin compound and an organic phosphite | |
US5854305A (en) | Plugging compound for chemical fastening | |
US20110073327A1 (en) | Two-component mortar composition and method of using same | |
KR900006254A (en) | Granite delicatessen | |
CO5040144A1 (en) | FOTOCURABLE COMPOSITION WITH USEFUL CYANOACRYLATE AS A GLUE, SEALANT OR COATING AND METHOD FOR POLYMERIZATION | |
JPS56141321A (en) | Photosetting resin composition | |
US20090308533A1 (en) | Fast-curing chemical fixing system and use thereof | |
GB1247422A (en) | Photocuring coating composition | |
JPS61243876A (en) | Adhesive based on acrylic compound | |
US5288767A (en) | Two-component adhesive composition for the chemical fixing technique | |
JPH06508871A (en) | A reagent kit for manufacturing a synthetic resin body that adhesively fixes the fixing element to the fixing base. | |
JPH0483100A (en) | Bolt fixing cartridge excellent in light resistance | |
US5047442A (en) | Photopolymerizable composition based on a vinyl compound, a sulfur-containing compound and an alpha-diketone | |
JPH01238656A (en) | High sensitive photopolymerizable composition | |
FI3712184T3 (en) | Fastening system comprising a curing component with at least one benzoate | |
JP2609060B2 (en) | Anchor cartridge | |
US4826888A (en) | Photopolymerizable composition | |
JP4093614B2 (en) | Adhesive composition | |
JP3565589B2 (en) | Fixing agent | |
JPH02269103A (en) | Photo-initiator mixture | |
KR910012809A (en) | Photocurable Urethane-Containing Compositions | |
AU702734B2 (en) | A Binder for building structures | |
JP4678984B2 (en) | Resin composition and injectable cartridge | |
JPS62161868A (en) | Photo-setting weather-resistant coating compound | |
JP3969791B2 (en) | Fixing composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081005 Year of fee payment: 14 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081005 Year of fee payment: 14 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091005 Year of fee payment: 15 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091005 Year of fee payment: 15 |
|
S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091005 Year of fee payment: 15 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101005 Year of fee payment: 16 |
|
EXPY | Cancellation because of completion of term | ||
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20101005 Year of fee payment: 16 |