JPS63359A - Synthetic resin composition - Google Patents
Synthetic resin compositionInfo
- Publication number
- JPS63359A JPS63359A JP14379586A JP14379586A JPS63359A JP S63359 A JPS63359 A JP S63359A JP 14379586 A JP14379586 A JP 14379586A JP 14379586 A JP14379586 A JP 14379586A JP S63359 A JPS63359 A JP S63359A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- weight
- silicon dioxide
- synthetic resin
- parts
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 25
- 229920003002 synthetic resin Polymers 0.000 title claims abstract description 18
- 239000000057 synthetic resin Substances 0.000 title claims abstract description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 18
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 18
- 239000003365 glass fiber Substances 0.000 claims abstract description 13
- 239000005662 Paraffin oil Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 abstract description 37
- 239000011347 resin Substances 0.000 abstract description 36
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 26
- 238000010079 rubber tapping Methods 0.000 abstract description 9
- 229920005601 base polymer Polymers 0.000 abstract description 6
- 239000000463 material Substances 0.000 abstract description 5
- 239000010690 paraffinic oil Substances 0.000 abstract description 5
- 229930182556 Polyacetal Natural products 0.000 abstract description 4
- 239000004952 Polyamide Substances 0.000 abstract description 4
- 229920002647 polyamide Polymers 0.000 abstract description 4
- 229920006324 polyoxymethylene Polymers 0.000 abstract description 4
- 238000002156 mixing Methods 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052681 coesite Inorganic materials 0.000 abstract 1
- 229910052906 cristobalite Inorganic materials 0.000 abstract 1
- 229910052682 stishovite Inorganic materials 0.000 abstract 1
- 229910052905 tridymite Inorganic materials 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 14
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 10
- 239000000835 fiber Substances 0.000 description 10
- 230000005484 gravity Effects 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 6
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 5
- 238000004898 kneading Methods 0.000 description 5
- 239000005062 Polybutadiene Substances 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 229920002857 polybutadiene Polymers 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 3
- 239000010692 aromatic oil Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- -1 polybutylene terephthalate Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 2
- CWGSOQVETBJTME-UHFFFAOYSA-N 3-(2-phenylethenyl)pyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C=CC=2C=CC=CC=2)=C1 CWGSOQVETBJTME-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 239000011145 styrene acrylonitrile resin Substances 0.000 description 2
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 229920001890 Novodur Polymers 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229920001895 acrylonitrile-acrylic-styrene Polymers 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 239000011163 secondary particle Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000000072 sodium resin Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、摺動特注、剛性ならびにタッピング強度に優
nる合成樹脂組放物に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Field of Application> The present invention relates to a synthetic resin assembly that has excellent sliding customization, rigidity, and tapping strength.
〈従来の技術〉
従来エリ、会fi5を樹脂に潤滑油を含有させることに
工り摺動特性の改善さnた組成物が得られることが知ら
nており、粉末状のポリアセタール又はポリアミドを用
いる方法(特公昭46−42217、特公昭46−53
21)、潤滑油をグラファイトや活性炭と併用する方法
(特開昭50−101051)などが提案されている。<Prior art> It has been known that a composition with improved sliding properties can be obtained by incorporating a lubricating oil into a resin, and it has been known that a composition with improved sliding properties can be obtained by using polyacetal or polyamide powder. Method (Special Publication No. 46-42217, Special Publication No. 46-53
21), a method of using lubricating oil in combination with graphite or activated carbon (Japanese Patent Laid-Open No. 101051/1983) has been proposed.
〈発明が解決しようとする問題点〉
しかしながら、従来の潤滑油含有樹脂組成物は摺動特性
において十分満足出来るものでなく、かつ剛性ならびV
cタッピング強度に劣るといった問題点を有していた。<Problems to be Solved by the Invention> However, conventional lubricating oil-containing resin compositions are not fully satisfactory in terms of sliding properties, and have poor rigidity and V.
It had the problem of poor tapping strength.
さらに、従来の組成物は、摺動特性の面よりポリアセタ
ール、ポリアミド、ポリカーボネート、ポリブチレンテ
レフタV−トZどの高価ナポリマーをベースとし、かつ
特殊な製造装置(混練機)全必要としたため組成物はひ
じように高価なものとなっていた0又、かかる組成物は
加工性においても劣っていたO
く問題点を解決するための手段〉
本発明者らは、摺動特性のみならず剛性ならびにタッピ
ング強度に優れる組成物であり、しかも安価で加工性に
優nるスチレン系樹脂をもベースポリマーとして用いる
ことができ、かつ通常の混練機で製造することができる
組成物に関し、鋭意研究した結果、本発明に到達したも
のである。Furthermore, from the standpoint of sliding properties, conventional compositions are based on expensive polymers such as polyacetal, polyamide, polycarbonate, and polybutylene terephthalate V-T-Z, and require special manufacturing equipment (kneading machines). Means for Solving the Problems The present inventors have developed not only sliding properties but also rigidity and The results of intensive research into a composition that has excellent tapping strength, can also use styrene resin, which is inexpensive and has excellent processability, as a base polymer, and can be manufactured using a normal kneading machine. , the present invention has been achieved.
すなわち、本発明は、曾底樹脂100重量部二酸化ケイ
素1〜20重量部、パラフィン系オイル1〜30重量部
およびガラス繊維1〜20重量部からなることを特徴と
する特許
性ならびにタッピング強度に優nる会成樹脂組成物を提
供するものである。That is, the present invention has excellent patentability and tapping strength, characterized by comprising 100 parts by weight of sodium resin, 1 to 20 parts by weight of silicon dioxide, 1 to 30 parts by weight of paraffin oil, and 1 to 20 parts by weight of glass fiber. The present invention provides a synthetic resin composition.
以下に本発明の会成樹脂組底物について詳細に説明する
。The composite resin composite sole of the present invention will be explained in detail below.
本発明において用いらnる合i樹脂としては、従来工り
摺動材料のベースポリマーとして用いらnでいるポリア
セタール、ボリアミド、ポリカーボネート、ポリブチレ
ンテレフタレートはもちろんのCと、塩化ビニル樹脂、
ポリスチレン(PS)、ゴム強化ポリスチレン(HI
PS )、スチレン−アクリロニトリル樹脂、スチレン
ー無水マレイン酸樹脂、スチレン−マレイミド樹脂、A
BS樹脂、M B S樹脂、AES樹脂、ACS樹脂、
AAS41脂、ポリエチレン、ポリプロピレン、ポリフ
ェニレンオキサイドナトが挙げられ、1種又は二種以上
用いることができる。The synthetic resins used in the present invention include not only polyacetal, polyamide, polycarbonate, and polybutylene terephthalate, which are conventionally used as base polymers for sliding materials, but also C, vinyl chloride resin,
Polystyrene (PS), rubber reinforced polystyrene (HI
PS ), styrene-acrylonitrile resin, styrene-maleic anhydride resin, styrene-maleimide resin, A
BS resin, MBS resin, AES resin, ACS resin,
Examples include AAS41 resin, polyethylene, polypropylene, and polyphenylene oxide, and one type or two or more types can be used.
特KPS,HIPS、スチレン−アクリロニトリル樹脂
、スチレンー無水マレイン酸樹脂、スチレン−マレイミ
ド樹脂、A B Si脂、M BS樹脂、AES樹脂、
ACS樹脂、A A S @脂などのスチレン系樹脂お
よびスチレン系樹脂と他樹脂との混合物が加工性ならび
に価格面より好ましい。Special KPS, HIPS, styrene-acrylonitrile resin, styrene-maleic anhydride resin, styrene-maleimide resin, AB Si resin, MBS resin, AES resin,
Styrenic resins such as ACS resin and AAS@resin, and mixtures of styrene resins and other resins are preferred from the viewpoint of processability and cost.
なお、スチレン系樹脂においては、スチレンの一部又は
全部をアルキル置換スチレン(αーメチルスチVン、p
−メチルスチレン等)に置、き換えることもできる。In addition, in styrene-based resins, some or all of the styrene is substituted with alkyl-substituted styrene (α-methylstyrene, p
-methylstyrene, etc.).
二酸化ケイ素とは、一般式SiO又にSIO2・nHt
oで示される化合物である。通常、10〜50mμの平
均一次粒子径(05〜75μの平均二次粒子径)を有す
る微粒子である。特にIii放物の加工性ならびに帯電
防止性の面より水分(105℃.2時間)が2〜10重
量係の含水二酸化ケイ素( S i O,・nH20)
が好1しい。Silicon dioxide has the general formula SiO or SIO2・nHt
This is a compound represented by o. Usually, they are fine particles having an average primary particle diameter of 10 to 50 μm (average secondary particle diameter of 05 to 75 μm). In particular, from the viewpoint of parabolic processability and antistatic properties, hydrated silicon dioxide (S i O, .nH20) with a water content of 2 to 10% by weight (105°C. 2 hours) is used.
is preferable.
二酸化ケイ素の用いら几る量は組成物の摺動特注、機械
的強度および加工性−により適宜選択することができる
が、曾成樹脂100重量部当り1〜20重量部である。The amount of silicon dioxide to be used can be appropriately selected depending on the sliding properties, mechanical strength, and processability of the composition, and is 1 to 20 parts by weight per 100 parts by weight of the resulting resin.
IM量郡部未満は摺動特性が、又20重量部を超えると
機械的強度が劣る。If the IM amount is less than 20 parts by weight, the sliding properties will be poor, and if it exceeds 20 parts by weight, the mechanical strength will be poor.
一般に潤滑油は、その構造エリアロマチック系オイル、
ナフテン系オイルおよびパラフィン系オイルに分類さn
る。又、それらは天然オイルお工び会成オイルに限らず
、その他の系を含むものであり、通常アロマチック系オ
イルとげアロマチック炭素が35i量チ以上のもの、ナ
フテン系オイルとにナフテン環炭素が30〜450〜4
5重量部およびパラフィン系オイルとはパラフィン鎖炭
素が50重量係以上のものを示す。In general, lubricating oils have a structure area of romatic oil,
Classified as naphthenic oil and paraffinic oil.
Ru. In addition, these oils are not limited to natural oils and manufactured oils, but also include other types of oils, and are usually aromatic oils with an aromatic carbon content of 35i or more, naphthenic oils, and naphthenic oils with naphthenic ring carbons. is 30-450-4
5 parts by weight and paraffin-based oil refer to those having 50 parts by weight or more of paraffin chain carbons.
本発明においては、パラフィン系オイルが必須成分であ
り、アロマテノク系オイルお工び/又はナフテン系オイ
ルでは、本発明の目的とする組成物は得られない。In the present invention, paraffinic oil is an essential component, and the composition targeted by the present invention cannot be obtained using aromatic oil or naphthenic oil.
最終PAi物の用いらnる用途ならびにベースポリマー
の種頌等にエリ、パラフィン系オイルの含有量は適宜選
択することができるが、摺動特性に優nる組成物を得る
ためKill、合5y.樹脂100重量部当り1〜30
重量部である。The content of paraffin oil can be selected as appropriate depending on the use of the final PAi product and the seed material of the base polymer. .. 1 to 30 per 100 parts by weight of resin
Parts by weight.
1重量部未満では摺動特性が、又30重置部を超えると
硬度および1′@熱性が劣る。If it is less than 1 part by weight, the sliding properties will be poor, and if it exceeds 30 parts by weight, the hardness and 1'@thermal properties will be poor.
特に、摺動特性ならびに機械的強度、さらには組成物の
製造面より、二酸fヒケイ素対パラフィン系オイルの重
全比が1=1〜3であ、るOとが好壕しい。In particular, from the viewpoint of sliding properties and mechanical strength, as well as the production of the composition, it is preferable that the total weight ratio of diacid f hysilicate to paraffinic oil is 1=1 to 3.
さらに、本発明において用いられるガラス繊維とは、単
繊維ならびに単懺維をシラン系お工び/又はクロム系の
集束削で処理してなるガラヌ繊維などであり、繊維長お
よび繊維径には制限にないが樹脂組成物の剛性、タッピ
ング強度、加工性等の面より繊維長3〜10−1繊維径
3〜20μであることが好ましい。なお、長繊維状で混
練された後、ペレット状にカットさnた樹脂組成物も本
発明には含inる。Furthermore, the glass fibers used in the present invention include galanic fibers made by treating single fibers and single fibers with silane-based machining/chromium-based focused cutting, and the fiber length and fiber diameter are limited. However, from the viewpoint of the rigidity, tapping strength, processability, etc. of the resin composition, it is preferable that the fiber length is 3 to 10<->1 and the fiber diameter is 3 to 20 .mu.m. Note that the present invention also includes a resin composition that is kneaded in the form of long fibers and then cut into pellets.
ガラス繊維の配合量は合成樹脂100重量部当り1〜2
0重量部である。1重量部未満では剛性とタッピング強
度に劣り、20重量部を越すと衝馨強度に劣る。The blending amount of glass fiber is 1 to 2 per 100 parts by weight of synthetic resin.
It is 0 parts by weight. If it is less than 1 part by weight, the rigidity and tapping strength will be poor, and if it exceeds 20 parts by weight, the impact strength will be poor.
本発明の什成樹脂組成物は、合成樹脂100重量部、二
酸化ケイ素1〜20]i量部、バラフィノ系オイル1〜
30重量部お工びガラス繊維1〜20重量部を一般的な
混、練機である一軸押り得らnる。The synthetic resin composition of the present invention includes 100 parts by weight of synthetic resin, 1 to 20 parts by weight of silicon dioxide, and 1 to 20 parts by weight of balafino oil.
30 parts by weight of glass fibers and 1 to 20 parts by weight of glass fibers are obtained by uniaxial extrusion using a general kneading and kneading machine.
用いらnる合成樹脂の形状には何ら制限はなく、粉末状
、ビーズ状、ベレット状、ダイス状等任意の形状のもの
を用いることができる。There is no restriction on the shape of the synthetic resin used, and any shape such as powder, beads, pellets, dice, etc. can be used.
さらに、混線時における合成樹脂、二酸化ケイ素、パラ
フィン系オイルおよびガラス繊維の混線順序には何ら制
限はない。Furthermore, there is no restriction on the order in which the synthetic resin, silicon dioxide, paraffin oil, and glass fiber are mixed.
なお、本発明の合成樹脂組成物に対し、着色剤、抗酸化
剤、紫外線吸収剤、難燃剤、充填剤、帯電防止剤等を適
宜配合することも可能である。It is also possible to appropriately blend colorants, antioxidants, ultraviolet absorbers, flame retardants, fillers, antistatic agents, etc. into the synthetic resin composition of the present invention.
以下に本発明を実施例でもって説明するが、本発明は0
2″Lによって何ら限定さnるものでない0
実施例−1
ABS樹脂、二酸化ケイ素(又は活性炭)、オイルおよ
びガラス繊維を田辺プラスチック社製−軸押出機(20
0℃)にて一括溶融混練し、組成物1〜8を得た。The present invention will be explained below with reference to examples.
0 Example-1 ABS resin, silicon dioxide (or activated carbon), oil and glass fiber were processed using a shaft extruder (20 mm) manufactured by Tanabe Plastic Co., Ltd.
0° C.) to obtain Compositions 1 to 8.
なお、組成物3と5Kに帯電防止剤を添加した0
得らnた組取物エリ東芝機械社製 IS 90B射出
取形機(200℃)にて各種試験片を詐取し、評価に供
した。In addition, various test pieces were obtained using an IS 90B injection molding machine (200°C) manufactured by Toshiba Machinery Co., Ltd. and used for evaluation. .
組成物の組成お工び評価結果全表−IK示す。Complete table of composition evaluation results of the composition - IK is shown.
oABs樹脂
アクリロニトリル25重量予、ブタジェン系ゴム10重
帝係およびスチレン65重量%からなる粉末状ABSグ
脂
〇二酸化ケイ素
■含水二酸fビケイ素(S i 02 ・nH20)S
i0293重量係以上重量比重120〜160y/M、
比表面積170〜210m” / y
■無水二酸化ケイ素(Sin2)
S102100M量予
0活 性 炭
比表面積600〜800 m’ / y、嵩比重380
〜450ノ/l
Oガラス繊維(シラン系集束剤で集束処理されたもの)
平均繊維長63、繊維径9μ
0オ イ ル
■パラフィン系オイル
比重0.8647、流動点−15℃、粘度(989℃)
5.18Cst、粘度比重恒数Q、7R96、C(A)
:3 %、 C(へ)): 27 %、C(Plニア
0 %
■アロマチック系オイル
比重1.0 O59、流動点15℃、粘度(98,9℃
) 32.63 Cst、粘度比重恒数0.954 F
t、C(〜:39%、C(ト)=29%、C(P):3
2%
■ナフテン系オイル
比重Q、 9051’l、流動点−20℃、粘度(98
,9℃)10.36Cst、粘度比重恒数0.1’+
417、C囚ニア係、C粂D:39チ、C(P):54
チ
0帯電防止剤
ミヨシ油脂社製
ダスパー125B
実施例−2
ABS樹脂、耐熱ABS樹脂、ABS樹脂、AAS樹脂
、二酸化ケイ素、パラフィン系オイルおよびガラス繊維
を田辺プラヌチック社製−軸押出機(200℃)にて一
括帛融混練し、組成物(A 9〜22)を得た。oABs Resin Powdered ABS gum resin consisting of 25% by weight of acrylonitrile, 10% by weight of butadiene rubber and 65% by weight of styrene 〇Silicon dioxide ■ Hydrous diacid f Bisilicon (S i 02 ・nH20)S
i0293 weight ratio or higher weight specific gravity 120-160y/M,
Specific surface area 170-210 m'/y ■Anhydrous silicon dioxide (Sin2) S102100M quantity 0 activity Carbon specific surface area 600-800 m'/y, bulk specific gravity 380
~450 no/l O glass fiber (bound with silane-based sizing agent) Average fiber length 63, fiber diameter 9μ 0 Oil ■Paraffin oil specific gravity 0.8647, pour point -15℃, viscosity (989) ℃)
5.18Cst, viscosity specific gravity constant Q, 7R96, C(A)
: 3%, C(to): 27%, C(Plnia 0% ■Aromatic oil specific gravity 1.0 O59, pour point 15℃, viscosity (98.9℃)
) 32.63 Cst, viscosity specific gravity constant 0.954 F
t, C (~: 39%, C (t) = 29%, C (P): 3
2% ■ Naphthenic oil specific gravity Q, 9051'l, pour point -20℃, viscosity (98
, 9℃) 10.36Cst, viscosity specific gravity constant 0.1'+
417, C Prisoner Near Section, C Kume D: 39 Chi, C(P): 54
Antistatic agent Dasper 125B manufactured by Miyoshi Oil Co., Ltd. Example-2 ABS resin, heat-resistant ABS resin, ABS resin, AAS resin, silicon dioxide, paraffin oil and glass fiber were processed using a shaft extruder (200°C) manufactured by Tanabe Planutik Co., Ltd. The mixture was melt-kneaded at once to obtain compositions (A 9-22).
実施例−1と同様にして組成物を評価した。The composition was evaluated in the same manner as in Example-1.
組成物の組成および評価結果を表−2に示す。The composition and evaluation results of the composition are shown in Table-2.
0合成樹脂
■ABS樹脂
アクリロニトリル23重量%、ブタジェン系ゴム10重
量%およびスチレン67重量受からなるペレット状AB
S樹脂
■耐熱ABS使脂−1
アクリロニトリル25重量比、ブタジェン系ゴム10重
量%、スチレン20重N %お工びα−メチルスチレン
45重量比からなるペレット状耐熱ABS、[脂
■耐熱ABSFE脂−2
アクリロニトリル10重量比、ブタジェン系ゴム10重
量比、スチレン量比重量係、N−フェニルマレイミド1
5重量%からなるペレット状耐熱ABS樹脂。0 Synthetic resin■ ABS resin Pellet-shaped AB consisting of 23% by weight of acrylonitrile, 10% by weight of butadiene rubber, and 67% by weight of styrene.
S Resin Heat-resistant ABS resin - 1 Pellet heat-resistant ABS made of 25% by weight of acrylonitrile, 10% by weight of butadiene rubber, 20% by weight of styrene and 45% by weight of α-methylstyrene, [Resin ■ Heat-resistant ABSFE resin - 2 Acrylonitrile 10 weight ratio, butadiene rubber 10 weight ratio, styrene amount ratio weight ratio, N-phenylmaleimide 1
Pellet-shaped heat-resistant ABS resin consisting of 5% by weight.
■AESAB
S樹脂ロニトリル23重量比、エチレンプロピレン系ゴ
ム10重8%、スチレン67重量%からなるペレット状
ABS樹脂。■AESAB S resin A pellet-shaped ABS resin consisting of 23% by weight of lonitrile, 10% by weight of ethylene propylene rubber, and 67% by weight of styrene.
■A A S樹脂
アクリロニトリル25重量比、アクリルエステル系ゴム
10ff(a%、スチレン65N量係からなるペレット
状AAsii脂。■A A S Resin Pellet-shaped AA resin consisting of 25% by weight of acrylonitrile, 10ff of acrylic ester rubber (a%, and 65N of styrene).
〇二酸化ケイ素:含水二酸化ケイ素
(S i02 ・nH20)
実施例−1と同一品
0ガラス繊維:実施例−1と同一品
0パラフィン系オイル:実施例−1と同一品・:ミ摺動
特注
テーパー摩耗試験機の摩耗輪の代りに直径11+sの鋼
球をセットした後、200ノの重りを掛け72 rpm
で、3脳浮の試験片上を5000回転させる。〇Silicon dioxide: Hydrous silicon dioxide (S i02 ・nH20) Same product as Example-1 0 Glass fiber: Same product as Example-1 0 Paraffin oil: Same product as Example-1 ・: Mi-sliding custom-made taper After setting a steel ball with a diameter of 11+s in place of the wear ring of the wear tester, a 200 kg weight was applied and the speed was set at 72 rpm.
Then, rotate the 3-brain floating test piece 5000 times.
摺動後の試験片の摩耗量を軌跡の深さで求めるO
軌跡の深さ・・・東京精密社製超粗さ計※タッピング強
度及び゛割れの有無
外径7膿φ、内径3.5朋φのボスに4祁φのビスをタ
ッピングしたときの空転する又は割れるまでの締付トル
クをトルクドライバーで測定、評価する。Determine the amount of wear on the test piece after sliding by the depth of the trajectory. Depth of the trajectory...Super roughness meter manufactured by Tokyo Seimitsu Co., Ltd. When tapping a 4mm diameter screw on a 4mm diameter boss, the tightening torque until it slips or breaks is measured and evaluated using a torque screwdriver.
〈発明の効果〉
本発明の曾成樹脂組成物は、摺動特注にもちろんのこと
、タッピング強度、剛性、加工性、着色性、帯電防止性
能に優れた材料である。<Effects of the Invention> The synthetic resin composition of the present invention is a material that is excellent in tapping strength, rigidity, workability, coloring property, and antistatic performance as well as being suitable for custom sliding applications.
また、本発明においては、従来用いら几でいた高価なベ
ースポリマーでなく、安価なスチレン系樹脂を用いるこ
とができ、樹脂の形状も粉末状に限らずベレット状のも
のも用いることができる。さらに、特殊な混練機を必要
とすることもないため、安価な材料を提供出来るもので
ある。Furthermore, in the present invention, an inexpensive styrene resin can be used instead of the expensive base polymer that has been conventionally used, and the shape of the resin is not limited to powder, but may also be in the form of a pellet. Furthermore, since no special kneading machine is required, an inexpensive material can be provided.
Claims (1)
部、パラフィン系オイル1〜30重量部およびガラス繊
維1〜20重量部からなることを特徴とする合成樹脂組
成物。 2)二酸化ケイ素がSiO_2・nH_2Oで示される
微粒子状の含水二酸化ケイ素である特許請求の範囲第1
項記載の合成樹脂組成物。Claims: 1) A synthetic resin composition comprising 100 parts by weight of a synthetic resin, 1 to 20 parts by weight of silicon dioxide, 1 to 30 parts by weight of paraffin oil, and 1 to 20 parts by weight of glass fiber. 2) Claim 1, wherein the silicon dioxide is fine particulate hydrated silicon dioxide represented by SiO_2.nH_2O.
Synthetic resin composition described in .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14379586A JPS63359A (en) | 1986-06-19 | 1986-06-19 | Synthetic resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14379586A JPS63359A (en) | 1986-06-19 | 1986-06-19 | Synthetic resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63359A true JPS63359A (en) | 1988-01-05 |
| JPH0523300B2 JPH0523300B2 (en) | 1993-04-02 |
Family
ID=15347160
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14379586A Granted JPS63359A (en) | 1986-06-19 | 1986-06-19 | Synthetic resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63359A (en) |
-
1986
- 1986-06-19 JP JP14379586A patent/JPS63359A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0523300B2 (en) | 1993-04-02 |
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