JPH039958B2 - - Google Patents
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- Publication number
- JPH039958B2 JPH039958B2 JP59151327A JP15132784A JPH039958B2 JP H039958 B2 JPH039958 B2 JP H039958B2 JP 59151327 A JP59151327 A JP 59151327A JP 15132784 A JP15132784 A JP 15132784A JP H039958 B2 JPH039958 B2 JP H039958B2
- Authority
- JP
- Japan
- Prior art keywords
- ferrocene
- molecular weight
- smoke
- composition
- liquid aliphatic
- 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.)
- Expired - Lifetime
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- Liquid Carbonaceous Fuels (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は減煙剤組成物に関し、詳しくは合成樹
脂、燃料油等を燃焼させた際に可及的に煙の発生
を低減させることのできる可燃性物質の減煙剤組
成物に関する。
従来、減煙剤としてビス(シクロペンタジエニ
ル)鉄()(一般にフエロセンと指称されてい
る。)が広く使用されている。しかしながら、フ
エロセンは昇華性を有する結晶性固体であるた
め、合成樹脂に配合した場合に分散性が悪く、ま
た時間の経過に伴ない昇華揮散するなどの欠点が
あつた。
この欠点を改善するため、フエロセン単体に代
えてn−ブチルフエロセンの如き液状フエロセン
誘導体を使用することが提案されている。この誘
導体は分散性は改善されるが、昇華性はそのまま
であり、揮散するという不都合は解決されなかつ
た。
また、フエロセンに液状ポリブタジエンなどを
反応させたものなどが提案されているが、減煙効
果が十分なものではなかつた。
そこで、本発明者らはこれらの欠点を解消し、
優れた減煙効果を有し、合成樹脂等への分散性が
良好で、昇華揮散しない減煙剤組成物を開発すべ
く鋭意検討した結果、フエロセンに特定の化合物
を配合することにより上記目的を達成しうること
を見出し、この知見に基いて本発明を完成した。
すなわち本発明は、ビス(シクロペンタジエニ
ル)鉄()および実質的に分子量140以上の成
分からなる液状脂肪族炭化水素よりなる減煙剤組
成物である。
本発明において用いられるビス(シクロペンタ
ジエニル)鉄()は一般にフエロセンと指称さ
れる化合物であり、2個のシクロペンタジエン環
の間に鉄原子()が挿入された構造を有する有
機鉄化合物である。しかし、このフエロセンは昇
華性であるため、本発明では、次の如き化合物と
配合せしめ、かかる欠点の解消を図るものであ
る。
次に、実質的に分子量が140以上の成分からな
る液状脂肪族炭化水素とは、分子量140未満のも
のが少量含まれていても良いが、大部分が分子量
140以上の液状脂肪族炭化水素であるものをいう。
この成分を配合することにより、フエロセンの減
煙効果を減少することなく昇華性を改善し得るの
である。分子量の上限は特に制限はないが、液状
であることから通常140〜2500程度のものが好適
に用いられる。
具体的には数平均分子量が140〜2500程度のイ
ソブテンオリゴマー、ドデカン、トリデカン、ポ
リブテンあるいはこれらの混合物などが挙げられ
る。特にイソブテンオリゴマーは熱により解重合
を生じ、非常に清浄な排ガスとなるため、好まし
い。
本発明においてフエロセンと実質的に分子量
140以上の成分からなる液状脂肪族炭化水素との
配合量については特に制限はなく、種々の割合に
て配合し得るものである。通常はフエロセン/液
状脂肪族炭化水素(重量比)=0.01〜500である。
特に本発明の組成物の可燃性物質に広く用いられ
るが、対象物質により好適な配合割合は異なる。
例えば合成樹脂等に使用する場合フエロセン/液
状脂肪族炭化水素(重量比)=0.01〜500、好まし
くは0.1〜100であり、燃料油等に使用する場合は
フエロセン/液状脂肪族炭化水素(重量比)=
0.01〜250、好ましくは0.05〜100である。その理
由は、合成樹脂等に配合する場合は粘性組成物と
することが好ましく、燃料油に加える場合は非粘
性組成物とすることが好ましいからである。
本発明の減煙剤組成物は、上記二成分を配合す
ることにより得られる。
このようにして得られた減煙剤組成物は種々の
可燃性物質、例えば合成樹脂のほか、灯油、軽油
等の燃料油などに使用することができる。
本発明の組成物は上記の如き可燃性物質に対し
て1〜1000ppm添加すれば良く、その結果、可燃
性物質の燃焼の際に煙の発生量を低減することが
できる。
また、合成樹脂などの可燃性物質に配合した場
合、本発明の組成物は分散性が良く、昇華揮散を
生じないため、減煙効果が持続する。
このように、本発明の減煙剤組成物は可燃性物
質、特に有害な煙を生ずる合成樹脂、燃料油など
に対して有効に使用することができる。
次に、実施例により本発明を詳しく説明する。
実施例 1〜3
第1表に示す各成分を所定量配合し、減煙剤組
成物を得た。得られた組成物を第1表に示す可燃
性物質に所定濃度となるように添加し、減煙効果
を測定した。結果を第1表に示す。
比較例 1
フエロセンにテトラエチルベンゼンを所定量配
合して組成物を得た。この組成物について実施例
1と同様に減煙効果を測定した。結果を第1表に
示す。
比較例 2
フエロセンにキシレンを所定量配合して組成物
を得た。この組成物について実施例3と同様に減
煙効果を測定した。結果を第1表に示す。キシレ
ンは蒸気圧が低いため、樹脂へ混練中に揮散し、
そのためフエロセンの分散が不十分であつた。
比較例 3
減煙剤としてn−ブチルフエロセンを用いたこ
と以外は実施例3と同様に減煙効果を測定した。
結果を第1表に示す。2−ブチルフエロセンは揮
発性があり、十分な減煙効果が得られなかつた。
The present invention relates to a smoke reducing agent composition, and more particularly to a smoke reducing agent composition for combustible materials that can reduce smoke generation as much as possible when synthetic resins, fuel oil, etc. are combusted. Conventionally, bis(cyclopentadienyl)iron (generally referred to as ferrocene) has been widely used as a smoke reducing agent. However, since ferrocene is a crystalline solid with sublimation properties, it has disadvantages such as poor dispersibility when blended into synthetic resins and sublimation and volatilization over time. In order to improve this drawback, it has been proposed to use a liquid ferrocene derivative such as n-butylferrocene in place of ferrocene alone. Although the dispersibility of this derivative is improved, the sublimation property remains unchanged, and the problem of volatilization remains unsolved. In addition, products in which ferrocene is reacted with liquid polybutadiene have been proposed, but the smoke reduction effect has not been sufficient. Therefore, the present inventors solved these drawbacks and
As a result of intensive studies to develop a smoke reducing agent composition that has an excellent smoke reducing effect, has good dispersibility in synthetic resins, etc., and does not sublimate or volatilize, we have found that the above objective can be achieved by blending a specific compound with ferrocene. We have discovered that this can be achieved, and based on this knowledge, we have completed the present invention. That is, the present invention is a smoke reducing agent composition comprising bis(cyclopentadienyl) iron () and a liquid aliphatic hydrocarbon consisting essentially of components having a molecular weight of 140 or more. Bis(cyclopentadienyl)iron ( ) used in the present invention is a compound generally referred to as ferrocene, and is an organic iron compound having a structure in which an iron atom ( ) is inserted between two cyclopentadiene rings. be. However, since this ferrocene is sublimable, the present invention attempts to eliminate this drawback by blending it with the following compounds. Next, liquid aliphatic hydrocarbons consisting essentially of components with a molecular weight of 140 or more are those that have a molecular weight of 140 or more, although a small amount of components with a molecular weight of less than 140 may be included.
140 or more liquid aliphatic hydrocarbons.
By blending this component, the sublimation properties of ferrocene can be improved without reducing the smoke reduction effect of ferrocene. There is no particular upper limit to the molecular weight, but since it is liquid, a molecular weight of about 140 to 2,500 is usually suitably used. Specifically, examples thereof include isobutene oligomers having a number average molecular weight of about 140 to 2,500, dodecane, tridecane, polybutene, or mixtures thereof. In particular, isobutene oligomers are preferable because they depolymerize due to heat and produce extremely clean exhaust gas. In the present invention, ferrocene and substantially molecular weight
There are no particular restrictions on the amount of liquid aliphatic hydrocarbons containing 140 or more components, and they can be blended in various ratios. Usually, the ratio of ferrocene/liquid aliphatic hydrocarbon (weight ratio) is 0.01 to 500.
In particular, it is widely used as a combustible substance in the composition of the present invention, but the suitable blending ratio varies depending on the target substance.
For example, when used in synthetic resins, ferrocene/liquid aliphatic hydrocarbon (weight ratio) = 0.01 to 500, preferably 0.1 to 100; when used in fuel oil, etc., ferrocene/liquid aliphatic hydrocarbon (weight ratio) )=
0.01-250, preferably 0.05-100. The reason for this is that it is preferable to form a viscous composition when blended into a synthetic resin or the like, and it is preferable to form a non-viscous composition when added to fuel oil. The smoke reducing agent composition of the present invention is obtained by blending the above two components. The smoke reducing agent composition thus obtained can be used for various combustible substances, such as synthetic resins and fuel oils such as kerosene and light oil. The composition of the present invention may be added in an amount of 1 to 1000 ppm to the above-mentioned combustible substances, and as a result, the amount of smoke generated during combustion of the combustible substances can be reduced. Further, when blended with a combustible substance such as a synthetic resin, the composition of the present invention has good dispersibility and does not sublimate and volatilize, so that the smoke reduction effect is maintained. As described above, the smoke reducing agent composition of the present invention can be effectively used for combustible substances, especially synthetic resins, fuel oils, etc. that generate harmful smoke. Next, the present invention will be explained in detail with reference to Examples. Examples 1 to 3 Each component shown in Table 1 was blended in a predetermined amount to obtain a smoke reducing agent composition. The obtained composition was added to the combustible substances shown in Table 1 to a predetermined concentration, and the smoke reduction effect was measured. The results are shown in Table 1. Comparative Example 1 A composition was obtained by blending a predetermined amount of tetraethylbenzene with ferrocene. The smoke reduction effect of this composition was measured in the same manner as in Example 1. The results are shown in Table 1. Comparative Example 2 A composition was obtained by blending xylene in a predetermined amount with ferrocene. The smoke reduction effect of this composition was measured in the same manner as in Example 3. The results are shown in Table 1. Since xylene has a low vapor pressure, it evaporates during kneading into the resin.
Therefore, the dispersion of ferrocene was insufficient. Comparative Example 3 The smoke reduction effect was measured in the same manner as in Example 3 except that n-butylferrocene was used as the smoke reduction agent.
The results are shown in Table 1. 2-Butylferrocene was volatile, and a sufficient smoke reduction effect could not be obtained.
【表】【table】
Claims (1)
び実質的に分子量140以上の成分からなる液状脂
肪族炭化水素よりなる減煙剤組成物。 2 実質的に分子量140以上の成分からなる液状
脂肪族炭化水素がイソブテンオリゴマー、ドデカ
ン、トリデカンあるいはポリブテンである特許請
求の範囲第1項記載の組成物。 3 ビス(シクロペンタジエニル)鉄()およ
び実質的に分子量140以上の成分からなる液状脂
肪族炭化水素の配合割合がビス(シクロペンタジ
エニル)鉄()/実質的に分子量140以上の成
分からなる液状脂肪族炭化水素=0.1〜500(重量
比)である特許請求の範囲第1項記載の組成物。[Scope of Claims] 1. A smoke reducing agent composition comprising bis(cyclopentadienyl) iron () and a liquid aliphatic hydrocarbon consisting essentially of a component having a molecular weight of 140 or more. 2. The composition according to claim 1, wherein the liquid aliphatic hydrocarbon consisting essentially of components having a molecular weight of 140 or more is isobutene oligomer, dodecane, tridecane, or polybutene. 3 The blending ratio of liquid aliphatic hydrocarbon consisting of bis(cyclopentadienyl) iron () and components with a molecular weight of 140 or more is bis(cyclopentadienyl) iron ()/components with a molecular weight of 140 or more The composition according to claim 1, wherein the liquid aliphatic hydrocarbon consists of 0.1 to 500 (weight ratio).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15132784A JPS6131492A (en) | 1984-07-23 | 1984-07-23 | Smoke-reducing agent composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15132784A JPS6131492A (en) | 1984-07-23 | 1984-07-23 | Smoke-reducing agent composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6131492A JPS6131492A (en) | 1986-02-13 |
JPH039958B2 true JPH039958B2 (en) | 1991-02-12 |
Family
ID=15516179
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15132784A Granted JPS6131492A (en) | 1984-07-23 | 1984-07-23 | Smoke-reducing agent composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6131492A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03244692A (en) * | 1990-02-23 | 1991-10-31 | Taiho Ind Co Ltd | Fuel additive |
US5713964A (en) * | 1993-10-25 | 1998-02-03 | Exxon Chemical Patents Inc. | Low smoke composition and firefighter training process |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5734317A (en) * | 1980-08-08 | 1982-02-24 | Hitachi Ltd | Clamping metal fittings for transformer iron core |
JPS5840390A (en) * | 1981-09-03 | 1983-03-09 | Chuo Kagaku Kenkyusho:Kk | Combustion auxiliary for gasoline or diesel engine |
-
1984
- 1984-07-23 JP JP15132784A patent/JPS6131492A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5734317A (en) * | 1980-08-08 | 1982-02-24 | Hitachi Ltd | Clamping metal fittings for transformer iron core |
JPS5840390A (en) * | 1981-09-03 | 1983-03-09 | Chuo Kagaku Kenkyusho:Kk | Combustion auxiliary for gasoline or diesel engine |
Also Published As
Publication number | Publication date |
---|---|
JPS6131492A (en) | 1986-02-13 |
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