CN103509283A - Blended easy-tearing wire cable material - Google Patents
Blended easy-tearing wire cable material Download PDFInfo
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- CN103509283A CN103509283A CN201310405070.0A CN201310405070A CN103509283A CN 103509283 A CN103509283 A CN 103509283A CN 201310405070 A CN201310405070 A CN 201310405070A CN 103509283 A CN103509283 A CN 103509283A
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- attapulgite
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- wire cable
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- 239000000463 material Substances 0.000 title claims abstract description 20
- 229960000892 attapulgite Drugs 0.000 claims abstract description 25
- 229910052625 palygorskite Inorganic materials 0.000 claims abstract description 25
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 14
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims abstract description 13
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920000915 polyvinyl chloride Polymers 0.000 claims abstract description 12
- 239000004800 polyvinyl chloride Substances 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 11
- 239000000843 powder Substances 0.000 claims abstract description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 10
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 244000226021 Anacardium occidentale Species 0.000 claims abstract description 7
- 239000004709 Chlorinated polyethylene Substances 0.000 claims abstract description 7
- 239000004698 Polyethylene Substances 0.000 claims abstract description 7
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 7
- 235000020226 cashew nut Nutrition 0.000 claims abstract description 7
- -1 polyethylene Polymers 0.000 claims abstract description 7
- 229920000573 polyethylene Polymers 0.000 claims abstract description 7
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 claims abstract description 5
- MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229920002367 Polyisobutene Polymers 0.000 claims abstract description 4
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 4
- OKISUZLXOYGIFP-UHFFFAOYSA-N 4,4'-dichlorobenzophenone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1=CC=C(Cl)C=C1 OKISUZLXOYGIFP-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims description 21
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 6
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 claims description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 6
- 230000003078 antioxidant effect Effects 0.000 claims description 6
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 6
- 239000012467 final product Substances 0.000 claims description 6
- 239000010881 fly ash Substances 0.000 claims description 6
- 238000009413 insulation Methods 0.000 claims description 6
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 6
- 239000000347 magnesium hydroxide Substances 0.000 claims description 6
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 6
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 229910052882 wollastonite Inorganic materials 0.000 claims description 6
- 239000010456 wollastonite Substances 0.000 claims description 6
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 3
- 235000021355 Stearic acid Nutrition 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 238000001816 cooling Methods 0.000 claims description 3
- 239000008367 deionised water Substances 0.000 claims description 3
- 229910021641 deionized water Inorganic materials 0.000 claims description 3
- SFNALCNOMXIBKG-UHFFFAOYSA-N ethylene glycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCO SFNALCNOMXIBKG-UHFFFAOYSA-N 0.000 claims description 3
- 238000010304 firing Methods 0.000 claims description 3
- 238000005469 granulation Methods 0.000 claims description 3
- 230000003179 granulation Effects 0.000 claims description 3
- 238000005984 hydrogenation reaction Methods 0.000 claims description 3
- 235000019359 magnesium stearate Nutrition 0.000 claims description 3
- 210000003205 muscle Anatomy 0.000 claims description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 3
- FIBARIGPBPUBHC-UHFFFAOYSA-N octyl 8-(3-octyloxiran-2-yl)octanoate Chemical compound CCCCCCCCOC(=O)CCCCCCCC1OC1CCCCCCCC FIBARIGPBPUBHC-UHFFFAOYSA-N 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 238000004513 sizing Methods 0.000 claims description 3
- 239000002002 slurry Substances 0.000 claims description 3
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 3
- 229910001948 sodium oxide Inorganic materials 0.000 claims description 3
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 claims description 3
- RRLOOYQHUHGIRJ-UHFFFAOYSA-M sodium;ethyl sulfate Chemical compound [Na+].CCOS([O-])(=O)=O RRLOOYQHUHGIRJ-UHFFFAOYSA-M 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- 239000008117 stearic acid Substances 0.000 claims description 3
- 239000011787 zinc oxide Substances 0.000 claims description 3
- NFVPEIKDMMISQO-UHFFFAOYSA-N 4-[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC=C(O)C=C1 NFVPEIKDMMISQO-UHFFFAOYSA-N 0.000 claims description 2
- 239000004593 Epoxy Substances 0.000 abstract 1
- 230000003712 anti-aging effect Effects 0.000 abstract 1
- 239000002131 composite material Substances 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 235000013773 glyceryl triacetate Nutrition 0.000 abstract 1
- IIGMITQLXAGZTL-UHFFFAOYSA-N octyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCC IIGMITQLXAGZTL-UHFFFAOYSA-N 0.000 abstract 1
- 239000010453 quartz Substances 0.000 abstract 1
- 229960002622 triacetin Drugs 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000032683 aging Effects 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
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- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Abstract
The invention discloses a blended easy-tearing wire cable material which is prepared from the raw materials of, by weight, 130-140 parts of SG-3 polyvinyl chloride, 1.2-1.5 parts of dioctyl phthalate, 6-8 parts of chlorinated polyethylene, 10-20 parts of calcium carbonate, 3-5 parts of polyethylene wax, 2-4 parts of cashew nut shell oil, 2.4-3.8 parts of an anti-aging agent AW, 1-2 parts of an accelerator NOBS, 1-2 parts of a curing agent DCBP, 2-4 parts of polyisobutylene, 1.2-1.5 parts of 2.4.6-tris(dimethylaminomethyl)phenol, 10-20 parts of modified attapulgite, 20-30 parts of a composite filler, 2-4 parts of titanium dioxide, 4-6 parts of quartz powder, 0.4-0.8 parts of glycerol triacetate, and 1.4-3 parts of epoxy octyl stearate.
Description
Technical field
The present invention relates to CABLE MATERIALS field, is exactly that wire cable material is easily torn in a kind of blend.
Background technology
Polyvinyl chloride cable material is the quality of PVC CABLE MATERIALS quality, is fundamentally to be filled a prescription and selected raw material decides by PVC CABLE MATERIALS.Along with continuous renewal and the development of various auxiliary agents and the weighting material of PVC, also make the formula of PVC CABLE MATERIALS constantly improve and improve.
Summary of the invention
The object of the present invention is to provide a kind of blend easily to tear wire cable material
Above-mentioned purpose realizes by following scheme:
Wire cable material is easily torn in a kind of blend, it is characterized in that: it is that raw material by following weight parts makes: SG-3 polyvinyl chloride 130-140, dioctyl phthalate (DOP) 1.2-1.5, chlorinatedpolyethylene 6-8, calcium carbonate 10-20, polyethylene wax 3-5, cashew nut shell oil 2-4, antioxidant A W2.4-3.8, accelerant NOBS 1-2, vulcanizing agent DCBP1-2, polyisobutene 2-4, 2.4.6-three (dimethylamino methyl) phenol 1.2-1.5, attapulgite modified 10-20, compounded mix 20-30, titanium dioxide 2-4, silica powder 4-6, Vanay 0.4-0.8, octyl epoxy stearate 1.4-3.
Described compounded mix is made by the raw material of following weight part:
Flyash 3-5, zinc oxide 1-2, wollastonite 3-4, white carbon black 1-2, stearic acid 1-2, wilkinite 5-10, white factice 1-2, zinc naphthenate 1-2, tributyl citrate 2-3, magnesium hydroxide 7-9;
The preparation method of described compounded mix calcines 2-3 hour by flyash, wollastonite, wilkinite at 700-850 ℃, then, take out, add in suitable quantity of water and grind in the lump with magnesium hydroxide, adding 10-15% hydrochloric acid soln tune PH is 5-5.5, and ground slurry is to 400-500 order, and repeated hydrogenation sodium oxide is adjusted to neutrality, spraying is dry, obtains powder; Gained powder is mixed with other remaining component, and ground and mixed evenly and get final product.
Attapulgite modified preparation method is:
(1) first, get attapulgite, at 700-800 ℃, calcine after 1-2 hour, take out, pulverize, cross 60-100 mesh sieve, then to add concentration be in the hydrogen peroxide of 1-2%, soaks after 8-12 hour, be dried;
(2) the 700-900 ℃ of sudden strain of a muscle in dodging firing of the dried attapulgite of step (1) burnt to 10-20 second, in attapulgite, pour the acetic acid solution that is equivalent to attapulgite weight 6-9 concentration 2-4mol/L doubly into again, under room temperature, stir 10-20 minute, soak again 2-4h, 1900-2800r/min centrifugal treating 10-19min, deionized water wash, oven dry;
(3) in the attapulgite after step (2) is processed, add and be equivalent to the clorafin of its weight 1-2%, after the Silane coupling agent KH550 of 1-2% stirs, pack reactor into, while being then warming up to 90-95 ℃, insulation 4-8 minute, add again the Magnesium Stearate that is equivalent to attapulgite weight 1-2%, the laureth sodium sulfovinate of 2-4%, is warming up to 120-130 ℃, insulation 8-15 minute, be cooled to 40-55 ℃, insulation 15-17 minute, takes out, after crossing 100-200 mesh sieve and get final product.
Wire cable material is easily torn in described a kind of blend, it is characterized in that:
Preparation method is:
(1) get SG-3 polyvinyl chloride, dioctyl phthalate (DOP), chlorinatedpolyethylene, calcium carbonate, polyethylene wax, cashew nut shell oil, antioxidant A W and mix by weight, in kneader, at 150-160 ℃, mediate after 5-12 minute, take out cooling;
(2) by the cooled sizing material of step (1) gained and each raw material blending of residue, mixing in twin screw extruder, granulation, control temperature 148-157 ℃, obtains finished product.
Beneficial effect of the present invention is: the present invention has increased the toughness of product, and transverse toughness is good, is not easy cracking, has improved the safety performance of product.
Embodiment
Wire cable material is easily torn in a kind of blend, it is that raw material by following weight parts (kg) makes: SG-3 polyvinyl chloride 140, dioctyl phthalate (DOP) 1.5, chlorinatedpolyethylene 8, calcium carbonate 18, polyethylene wax 5, cashew nut shell oil 4, antioxidant A W3.5, accelerant NOBS 1.6, vulcanizing agent DCBP1.4, polyisobutene 4,2.4.6-tri-(dimethylamino methyl) phenol 1.5, attapulgite modified 18, compounded mix 26, titanium dioxide 3, silica powder 5, Vanay 0.8, octyl epoxy stearate 1.8.
Described compounded mix is made by the raw material of following weight part:
Flyash 5, zinc oxide 2, wollastonite 4, white carbon black 2, stearic acid 1, wilkinite 10, white factice 2, zinc naphthenate 2, tributyl citrate 2, magnesium hydroxide 9;
The preparation method of described compounded mix calcines flyash, wollastonite, wilkinite 3 hours at 750 ℃, then, take out, add in suitable quantity of water and grind in the lump with magnesium hydroxide, adding 15% hydrochloric acid soln tune PH is 5, and after ground slurry to 500 order, repeated hydrogenation sodium oxide is adjusted to neutrality, spraying is dry, obtains powder; Gained powder is mixed with other remaining component, and ground and mixed evenly and get final product.
Attapulgite modified preparation method is:
(1) first, get attapulgite, at 800 ℃, calcine after 2 hours, take out, pulverize, cross 60 mesh sieves, then to add concentration be, in 2% hydrogen peroxide, to soak after 12 hours, dry;
(2) the 900 ℃ of sudden strains of a muscle in dodging firing of the dried attapulgite of step (1) are burnt 10 seconds, again to the acetic acid solution of pouring the concentration 4mol/L that is equivalent to 8 times of attapulgite weight in attapulgite into, under room temperature, stir 18 minutes, soak again 3h, 2200r/min centrifugal treating 19min, deionized water wash, oven dry;
(3) after adding the clorafin, 2% the Silane coupling agent KH550 that are equivalent to its weight 2% to stir in the attapulgite after step (2) is processed, pack reactor into, while being then warming up to 95 ℃, be incubated 7 minutes, add again the Magnesium Stearate that is equivalent to attapulgite weight 1.5%, 3% laureth sodium sulfovinate, is warming up to 130 ℃, is incubated 15 minutes, be cooled to 55 ℃, be incubated 17 minutes, take out, after crossing 200 mesh sieves and get final product.
Wire cable material is easily torn in described a kind of blend, and preparation method is:
(1) get SG-3 polyvinyl chloride, dioctyl phthalate (DOP), chlorinatedpolyethylene, calcium carbonate, polyethylene wax, cashew nut shell oil, antioxidant A W and mix by weight, in kneader, at 160 ℃, mediate after 12 minutes, take out cooling;
(2) by the cooled sizing material of step (1) gained and each raw material blending of residue, mixing in twin screw extruder, granulation, control 157 ℃ of temperature, obtains finished product.
The present embodiment is carried out to performance test, and the data obtained is as follows:
From the present embodiment test result, product of the present invention is through the aging of 100 ℃ * 168h and 80 ℃ * 6h Apparatus for Pressure at high-temp, its mechanical and physical performance variation meets corresponding mark requirement, has good physical and mechanical properties, meets the demand of differing temps environmental change.
Claims (2)
1. wire cable material is easily torn in a blend, it is characterized in that: it is that raw material by following weight parts makes: SG-3 polyvinyl chloride 130-140, dioctyl phthalate (DOP) 1.2-1.5, chlorinatedpolyethylene 6-8, calcium carbonate 10-20, polyethylene wax 3-5, cashew nut shell oil 2-4, antioxidant A W 2.4-3.8, accelerant NOBS 1-2, vulcanizing agent DCBP 1-2, polyisobutene 2-4, 2.4.6-three (dimethylamino methyl) phenol 1.2-1.5, attapulgite modified 10-20, compounded mix 20-30, titanium dioxide 2-4, silica powder 4-6, Vanay 0.4-0.8, octyl epoxy stearate 1.4-3,
Described compounded mix is made by the raw material of following weight part:
Flyash 3-5, zinc oxide 1-2, wollastonite 3-4, white carbon black 1-2, stearic acid 1-2, wilkinite 5-10, white factice 1-2, zinc naphthenate 1-2, tributyl citrate 2-3, magnesium hydroxide 7-9;
The preparation method of described compounded mix calcines 2-3 hour by flyash, wollastonite, wilkinite at 700-850 ℃, then, take out, add in suitable quantity of water and grind in the lump with magnesium hydroxide, adding 10-15% hydrochloric acid soln tune PH is 5-5.5, and ground slurry is to 400-500 order, and repeated hydrogenation sodium oxide is adjusted to neutrality, spraying is dry, obtains powder; Gained powder is mixed with other remaining component, and ground and mixed evenly and get final product;
Attapulgite modified preparation method is:
(1) first, get attapulgite, at 700-800 ℃, calcine after 1-2 hour, take out, pulverize, cross 60-100 mesh sieve, then to add concentration be in the hydrogen peroxide of 1-2%, soaks after 8-12 hour, be dried;
(2) the 700-900 ℃ of sudden strain of a muscle in dodging firing of the dried attapulgite of step (1) burnt to 10-20 second, in attapulgite, pour the acetic acid solution that is equivalent to attapulgite weight 6-9 concentration 2-4mol/L doubly into again, under room temperature, stir 10-20 minute, soak again 2-4h, 1900-2800r/min centrifugal treating 10-19min, deionized water wash, oven dry;
(3) in the attapulgite after step (2) is processed, add and be equivalent to the clorafin of its weight 1-2%, after the Silane coupling agent KH550 of 1-2% stirs, pack reactor into, while being then warming up to 90-95 ℃, insulation 4-8 minute, add again the Magnesium Stearate that is equivalent to attapulgite weight 1-2%, the laureth sodium sulfovinate of 2-4%, is warming up to 120-130 ℃, insulation 8-15 minute, be cooled to 40-55 ℃, insulation 15-17 minute, takes out, after crossing 100-200 mesh sieve and get final product.
2. wire cable material is easily torn in a kind of blend according to claim 1, it is characterized in that:
Preparation method is:
(1) get SG-3 polyvinyl chloride, dioctyl phthalate (DOP), chlorinatedpolyethylene, calcium carbonate, polyethylene wax, cashew nut shell oil, antioxidant A W and mix by weight, in kneader, at 150-160 ℃, mediate after 5-12 minute, take out cooling;
(2) by the cooled sizing material of step (1) gained and each raw material blending of residue, mixing in twin screw extruder, granulation, control temperature 148-157 ℃, obtains finished product.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310405070.0A CN103509283B (en) | 2013-09-06 | 2013-09-06 | One is blended easily tears wire cable material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310405070.0A CN103509283B (en) | 2013-09-06 | 2013-09-06 | One is blended easily tears wire cable material |
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| Publication Number | Publication Date |
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| CN103509283A true CN103509283A (en) | 2014-01-15 |
| CN103509283B CN103509283B (en) | 2016-01-20 |
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| CN201310405070.0A Expired - Fee Related CN103509283B (en) | 2013-09-06 | 2013-09-06 | One is blended easily tears wire cable material |
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Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103980602A (en) * | 2014-04-18 | 2014-08-13 | 力拓电力合金电缆股份有限公司 | Acid-resistant cable material |
| CN104119571A (en) * | 2014-06-26 | 2014-10-29 | 合肥和安机械制造有限公司 | Special reinforcing filler for high-pressure rubber tubes and preparation method thereof |
| CN104119572A (en) * | 2014-06-26 | 2014-10-29 | 合肥和安机械制造有限公司 | Special packing for wear-resistant and corrosion-resistant high-pressure rubber pipe and preparation method of special packing |
| CN104151609A (en) * | 2014-06-26 | 2014-11-19 | 合肥和安机械制造有限公司 | Special packing for antibacterial high-strength high-pressure rubber tube and preparation method of packing |
| CN105061932A (en) * | 2015-08-05 | 2015-11-18 | 安徽电信器材贸易工业有限责任公司 | Blended easily torn electric wire cable material |
| CN105482204A (en) * | 2015-12-15 | 2016-04-13 | 中冠电缆有限公司 | Neoprene cable material containing modified cotton linters and preparation method thereof |
| CN105542347A (en) * | 2016-01-25 | 2016-05-04 | 安徽华泰电缆科技有限公司 | Cable material formula |
| CN105969183A (en) * | 2016-05-26 | 2016-09-28 | 合肥市田源精铸有限公司 | Automobile antirust wax with high strength |
| CN106098234A (en) * | 2016-06-24 | 2016-11-09 | 浙江英美达电缆科技有限公司 | A kind of aluminium alloy power cable of anti-long-term ultraviolet ageing |
| CN106432985A (en) * | 2016-11-24 | 2017-02-22 | 安徽意力电缆有限公司 | PVC (polyvinyl chloride) cable material formulation |
| CN107556661A (en) * | 2017-09-30 | 2018-01-09 | 四会市启德信息咨询服务有限公司 | A kind of wear-resistant cable material and preparation method thereof |
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| CN102964666A (en) * | 2012-10-31 | 2013-03-13 | 安徽省易达电子有限公司 | Capacitor film containing modified bentonite and preparation method thereof |
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- 2013-09-06 CN CN201310405070.0A patent/CN103509283B/en not_active Expired - Fee Related
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| JP2005126617A (en) * | 2003-10-24 | 2005-05-19 | Daiso Co Ltd | Composition for curing chlorinated polyethylene |
| CN102382381A (en) * | 2011-11-15 | 2012-03-21 | 中天科技装备电缆有限公司 | High water resistance degaussing cable sheath material and preparation method thereof |
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Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103980602A (en) * | 2014-04-18 | 2014-08-13 | 力拓电力合金电缆股份有限公司 | Acid-resistant cable material |
| CN104119571A (en) * | 2014-06-26 | 2014-10-29 | 合肥和安机械制造有限公司 | Special reinforcing filler for high-pressure rubber tubes and preparation method thereof |
| CN104119572A (en) * | 2014-06-26 | 2014-10-29 | 合肥和安机械制造有限公司 | Special packing for wear-resistant and corrosion-resistant high-pressure rubber pipe and preparation method of special packing |
| CN104151609A (en) * | 2014-06-26 | 2014-11-19 | 合肥和安机械制造有限公司 | Special packing for antibacterial high-strength high-pressure rubber tube and preparation method of packing |
| CN105061932A (en) * | 2015-08-05 | 2015-11-18 | 安徽电信器材贸易工业有限责任公司 | Blended easily torn electric wire cable material |
| CN105482204A (en) * | 2015-12-15 | 2016-04-13 | 中冠电缆有限公司 | Neoprene cable material containing modified cotton linters and preparation method thereof |
| CN105542347A (en) * | 2016-01-25 | 2016-05-04 | 安徽华泰电缆科技有限公司 | Cable material formula |
| CN105969183A (en) * | 2016-05-26 | 2016-09-28 | 合肥市田源精铸有限公司 | Automobile antirust wax with high strength |
| CN106098234A (en) * | 2016-06-24 | 2016-11-09 | 浙江英美达电缆科技有限公司 | A kind of aluminium alloy power cable of anti-long-term ultraviolet ageing |
| CN106432985A (en) * | 2016-11-24 | 2017-02-22 | 安徽意力电缆有限公司 | PVC (polyvinyl chloride) cable material formulation |
| CN107556661A (en) * | 2017-09-30 | 2018-01-09 | 四会市启德信息咨询服务有限公司 | A kind of wear-resistant cable material and preparation method thereof |
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