JPS5839436A - Rubber plug - Google Patents
Rubber plugInfo
- Publication number
- JPS5839436A JPS5839436A JP13885181A JP13885181A JPS5839436A JP S5839436 A JPS5839436 A JP S5839436A JP 13885181 A JP13885181 A JP 13885181A JP 13885181 A JP13885181 A JP 13885181A JP S5839436 A JPS5839436 A JP S5839436A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- mixture
- hardness
- organic peroxide
- plug
- 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
- 229920001971 elastomer Polymers 0.000 title claims abstract description 5
- 239000000203 mixture Substances 0.000 claims abstract description 16
- 150000001451 organic peroxides Chemical class 0.000 claims abstract description 7
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 239000000126 substance Substances 0.000 abstract description 8
- 239000003431 cross linking reagent Substances 0.000 abstract description 6
- 239000003814 drug Substances 0.000 abstract description 6
- 238000004132 cross linking Methods 0.000 abstract description 5
- 229940079593 drug Drugs 0.000 abstract description 5
- 238000002347 injection Methods 0.000 abstract description 3
- 239000007924 injection Substances 0.000 abstract description 3
- 229920000459 Nitrile rubber Polymers 0.000 abstract 2
- 229920005555 halobutyl Polymers 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 9
- 239000011593 sulfur Substances 0.000 description 9
- 229910052717 sulfur Inorganic materials 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 7
- 238000004073 vulcanization Methods 0.000 description 7
- 230000000704 physical effect Effects 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 238000005987 sulfurization reaction Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 210000001520 comb Anatomy 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 241001573498 Compacta Species 0.000 description 1
- 241000425362 Hydrium Species 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 208000012868 Overgrowth Diseases 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229920001821 foam rubber Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/02—Copolymers with acrylonitrile
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L23/28—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or halogen-containing compounds
- C08L23/283—Iso-olefin halogenated homopolymers or copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は注射薬、試薬、化字薬晶叫′に使用される溶出
智の少ない耐油性のコムぜんに関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an oil-resistant composition with a small dissolution rate, which is used in injection drugs, reagents, and pharmaceutical crystals.
従来油を主成分又は分散剤とし、前記薬品に使用されて
いるコムぜんはニトリルコム(以下NBI(と記す)が
主成分で、その架橋剤としては一般に硫黄及び加硫促進
剤が用いられているが、油のsewによって経時的に架
橋剤が溶出し、薬品として純度が低下するかど安全性に
欠けるものである。又蛾近医薬品は異物の少ない高品質
のものが要求され、それに伴い容器によっても異物の発
生しないことが条件になってきたので、コムぜんも当然
溶出物が従来のものより更に少ない材質のものが要求さ
れるようになってき喪。Conventionally, the compositions used in the above chemicals have oil as the main component or dispersant, and nitrile comb (hereinafter referred to as NBI) is the main component, and sulfur and vulcanization accelerators are generally used as crosslinking agents. However, as the oil sews, the crosslinking agent elutes over time, reducing the purity of the drug and making it unsafe.Furthermore, high-quality drugs with few foreign substances are required, and as a result, containers are As it has become a requirement that no foreign matter be generated, it is natural that materials with even fewer eluable materials than conventional ones are required.
コムぜんからの溶出物の発生社主として硫黄及び加硫促
進剤によるものであるが、この溶出物を多くする原因が
補強剤等信の配合剤にあるならば、これを減少させるこ
とは出来るが、硫黄及び加硫促進剤の場合はこれを減少
すれば加硫しなくなり、又物性も低下し、混合物中の配
、合剤の溶出が容易となる0又増置すると物性社向上し
混合物中の配合剤の溶出はなくなるが、過剰の硫黄及び
加硫促進剤が溶出してくるし、硬さが上シ過ぎてコムぜ
んの特性としての針刺性が悪くなってくる。The generation of eluates from combustible materials is mainly due to sulfur and vulcanization accelerators, but if the cause of the increase in eluables is due to the additives in reinforcing agents, this can be reduced. In the case of sulfur and vulcanization accelerators, if they are reduced, vulcanization will not occur and the physical properties will also decrease, making it easier to mix and elute the mixture. Although the elution of the compounding ingredients disappears, excess sulfur and vulcanization accelerator are eluted, and the hardness is too high, resulting in poor needle stickiness, which is a characteristic of combs.
即ち、架橋剤の通合を決めることが、コムぜんの優劣を
決める要因となっている。In other words, determining the suitability of the crosslinking agent is a factor that determines the superiority or inferiority of the composition.
通常はjム成分ioo*緻部に対して硫黄及び有機促進
剤は3〜6腫象部とされる。その1例として従来のコム
ぜんの配合及び性能を第1表に示す。Usually, sulfur and organic accelerators are added to 3 to 6 tumor areas for each mass component ioo * pars compacta. As an example, the formulation and performance of conventional comzen are shown in Table 1.
第 1 表
(配合) 重
量部NBR(JARN 2308日本合成jム■コム
1o。Table 1 (Formulation) Part by weight NBR (JARN 2308 Nippon Gosei Jmu■com
1 o.
シリカ(Nlpsil VN−3目本シリカ■製)20
プロセスオイル(コモレックス2号日不石油■製)
5顔料(カーポジづ5−)り昭和電工■製)
0.2醗化亜鉛(亜鉛華1号堺化学■製)
3硫黄(微粉硫黄細井化学■製)
2加硫促進剤(ツクセラーDN大内新興化学■
製)1.5加硫促逸剤(ノクセ5−TT大内新興化学■
製)0.5計 132.2重量部
(物性)
硬さ 50過マシ
ガシ酸力リウム還元性物質 8.5
−可視部透過率430μ島
93.0%オレイン醗エチル浸漬硬さ変化
6一方、架橋剤として有様過酸化物を使用する
場合は、その使用量が少なく、2重置部以下で充分に効
果が発揮でき、従って溶出物も少なくなる。第2表にそ
の一例を示す。Silica (made by Nlpsil VN-3 Memoto Silica ■) 20
Process oil (Comolex No. 2 manufactured by Nippon Oil Co., Ltd.)
5 Pigments (Carposis 5-) manufactured by Showa Denko)
0.2 zinc oxide (zinc oxide No. 1 manufactured by Sakai Chemical Co., Ltd.)
3 Sulfur (fine sulfur manufactured by Hosoi Chemical)
2 Vulcanization accelerator (Tsukusera DN Ouchi Shinko Chemical)
) 1.5 vulcanization accelerator (Noxe 5-TT Ouchi Shinko Chemical)
(manufactured by) 0.5 total 132.2 parts by weight (physical properties) Hardness 50% hydrium acid reducing substance 8.5
-Visible transmittance 430μ
93.0% olein ethyl immersion hardness change
6. On the other hand, when a modified peroxide is used as a crosslinking agent, the amount used is small and the effect can be sufficiently exerted with less than double placement, so that the eluate is also reduced. An example is shown in Table 2.
第 2 表
(配合) 重
量部NBR(纂1表と同じもの)
to。Table 2 (composition) Part by weight NBR (same as Table 1)
to.
シリカ(第1表と同じもの)20
づ0セスオイル(第1表と同じもの)
5有機過陵化物(バーへ中+j2.5B日本油脂■
製) 1計 126重量部
(物性)
硬さ 53過マ:
Jガン酸カリウム還元性物質 6
.5−可視部透過率
99.2%即ち有機過酸化物による架橋は硫黄架
橋に比べて溶出物が少ないか第2表のような配合でコム
せんt−製造すると、硬さが岐く、針刺時にコム片発生
が見られる@一般に架橋剤として有様過酸化物は硫黄に
比較して引裂抵抗が小さく、コムぜんの針刺性に対して
好ましくない@本発明者勢はこの点を改良すべ(、NB
Rに対しハロゲシ化ブチルコムをプレシトすることに着
目した。有機過酸化物に対し、NBHの架橋効率は1.
0であり、ハ0ゲシ化づチルコムは0.5である。即ち
、NBRFiハ0ゲシ化づチルコムに比べて架橋しにく
く、従って硬さも小さい値を示す。即ちNBRとへ〇ゲ
シ化ブチルコムの割合を変えれば、硬さが変わることを
見出した0これをコムせ元に応用すれば溶出物の少々い
材質が得られると考え、そのプレシト比について検討を
行い、次の結果を得た。即ち、
NBR70〜90重量%
ハ0ゲシ化づチjLlム 10〜300〜30重
量部ら遷ばれたプレシトコムを使用した場合、その架橋
物は溶出物が少なく買物性が優れていることが判った。Silica (same as in Table 1) 20% Sesoil (same as in Table 1)
5 organic overgrowth compound (bar medium+j2.5B Nippon Oil & Fats ■
(manufactured by) 1 total 126 parts by weight (physical properties) Hardness 53%:
J Potassium Ganate Reducing Substance 6
.. 5-Visible transmittance
99.2%, that is, cross-linking with organic peroxide has less eluate than cross-linking with sulfur.If the composition shown in Table 2 is used to produce combs, the hardness will be low and comb pieces will be generated when punctured. Generally, modified peroxides as crosslinking agents have lower tear resistance than sulfur and are unfavorable for the needle stickiness of the composition.The present inventors should improve this point (, NB
We focused on precipitating halogenated butylcomb to R. The crosslinking efficiency of NBH is 1.
0, and 0.5 is 0.5. That is, it is more difficult to crosslink than NBRFi halogenated butylcomb, and therefore exhibits a smaller hardness value. In other words, we found that the hardness changes by changing the ratio of NBR and butyl comb.We thought that if we applied this to a comb base, we could obtain a material with a little less eluate, so we investigated the precipitate ratio. and obtained the following results. In other words, it was found that when using Precitocom, which was composed of 70 to 90 weight percent NBR and 10 to 300 to 30 parts by weight, the crosslinked product had less eluate and was superior in shopping properties. .
即ぢハ0ゲシ化ブチルコムがlO重重置風下では、硬さ
の低下は見られず、又300重量部上では礎さの低下が
大きく、物性も悪化する。この際有機過酸化物を増量し
ても、殆んど効果は認められず、溶出物は逆に増加して
くる。When the butyl comb is placed under 10 parts by weight, no decrease in hardness is observed, and above 300 parts by weight, the hardness decreases significantly and the physical properties deteriorate. At this time, even if the amount of organic peroxide is increased, almost no effect is observed, and on the contrary, the amount of eluate increases.
又、 NBFtのニトリル量が25重緻襲以下となると
、製品の耐油性が低下し、市販の油性医薬品に適合しな
くなる。Furthermore, if the amount of nitrile in NBFt is less than 25 times, the oil resistance of the product will decrease and it will not be compatible with commercially available oil-based pharmaceuticals.
実施例
第3表は示す配合物を有機過酸化−で架橋し、その製品
の物性を測定し、第3表にこれを示し九〇
第 3 表
NBR(第1表と同じ) 95 80 −
80 65シリカ(第1表と同じ) 10
10 10 10硬さ 5
2 44 45 32過マシガン酸カリウ」元性物
質−g) 6.5 6.5 6.3
9.0可視部透過率430p%%) 99
.0 99.8 99.8 90オレイ」エチル浸漬(
硬さダヒ)”’ 4” 6 ’10
針刺性 可 ” 優 優 良A1
の比較例においては溶′出物は少ないが、峡さが硬く、
針刺性が最も悪い。又A4の比較例では溶出物が多く、
岐さが低く、針刺性は本発明より劣る。本発明A2及び
罵3は溶出物も少なく、硬さも適当で、その針刺性は優
れている。Examples Table 3 shows the formulations shown in Table 3, which were cross-linked with organic peroxide, and the physical properties of the products were measured, which are shown in Table 3.
80 65 Silica (same as Table 1) 10
10 10 10 Hardness 5
2 44 45 32 Potassium permasiganate (g) 6.5 6.5 6.3
9.0 visible part transmittance 430p%%) 99
.. 0 99.8 99.8 90 Olay” ethyl immersion (
Hardness)"'4"6'10
Needle stickability: Good ” Excellent Good A1
In the comparative example, there was little eluate, but the gorge was hard and
Worst needle stickiness. In addition, in the comparative example of A4, there were many eluted substances,
The branching is low, and the needle stickability is inferior to that of the present invention. Inventions A2 and 3 have little eluate, appropriate hardness, and excellent needle stickability.
以上のようにNBRにハロゲシ化コムを混合し716成
分の配合物を有機過酸化物で架橋したゴムぜんは溶出物
が少なく針刺性尋の物性及び油との接触性に優れたもの
であり注射薬、試薬、化学薬品用のゴムぜんとして有用
である〇193−As mentioned above, rubber foam made by mixing NBR with halogenated comb and cross-linking the 716-component mixture with organic peroxide has few eluates and has excellent physical properties of needle stickiness and contact with oil. Useful as rubber for injection drugs, reagents, and chemicals〇193-
Claims (1)
lO〜301iJ1%の混合物をゴム成分とする配合物
を有機過酸化物で架橋させたことを特徴とするコムぜん
。A composition characterized in that a rubber component is a mixture of 0 to 90 % of Nitsil 16F and 1 % of butyl halogenide 1O to 301iJ, which is crosslinked with an organic peroxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13885181A JPS5839436A (en) | 1981-09-03 | 1981-09-03 | Rubber plug |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13885181A JPS5839436A (en) | 1981-09-03 | 1981-09-03 | Rubber plug |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5839436A true JPS5839436A (en) | 1983-03-08 |
Family
ID=15231644
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13885181A Pending JPS5839436A (en) | 1981-09-03 | 1981-09-03 | Rubber plug |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5839436A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1544242A1 (en) * | 2003-08-14 | 2005-06-22 | Bayer Inc. | Butyl compositions comprising nitrile polymers |
JP2006052327A (en) * | 2004-08-12 | 2006-02-23 | Fujikura Rubber Ltd | DME resistant rubber composition |
US8709603B2 (en) | 2007-07-30 | 2014-04-29 | Michel Oulie | Article based on a composition containing a crosslinked blend of elastomers |
US10099821B2 (en) | 2014-09-16 | 2018-10-16 | Sumitomo Rubber Industries, Ltd. | Method for manufacturing a medical rubber closure |
DE112017001158T5 (en) | 2016-04-27 | 2018-11-22 | Kelk Ltd. | Optical sensor |
CN109593280A (en) * | 2018-12-26 | 2019-04-09 | 湖北华强科技有限责任公司 | A kind of chlorinated butyl rubber bung formula and preparation method |
-
1981
- 1981-09-03 JP JP13885181A patent/JPS5839436A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1544242A1 (en) * | 2003-08-14 | 2005-06-22 | Bayer Inc. | Butyl compositions comprising nitrile polymers |
JP2006052327A (en) * | 2004-08-12 | 2006-02-23 | Fujikura Rubber Ltd | DME resistant rubber composition |
JP4531483B2 (en) * | 2004-08-12 | 2010-08-25 | 藤倉ゴム工業株式会社 | Rubber member |
US8709603B2 (en) | 2007-07-30 | 2014-04-29 | Michel Oulie | Article based on a composition containing a crosslinked blend of elastomers |
US10099821B2 (en) | 2014-09-16 | 2018-10-16 | Sumitomo Rubber Industries, Ltd. | Method for manufacturing a medical rubber closure |
DE112017001158T5 (en) | 2016-04-27 | 2018-11-22 | Kelk Ltd. | Optical sensor |
CN109593280A (en) * | 2018-12-26 | 2019-04-09 | 湖北华强科技有限责任公司 | A kind of chlorinated butyl rubber bung formula and preparation method |
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