CN105440427A - Clutch cable joint and preparation method thereof - Google Patents
Clutch cable joint and preparation method thereof Download PDFInfo
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- CN105440427A CN105440427A CN201510976296.5A CN201510976296A CN105440427A CN 105440427 A CN105440427 A CN 105440427A CN 201510976296 A CN201510976296 A CN 201510976296A CN 105440427 A CN105440427 A CN 105440427A
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- consumption
- cable joint
- weight part
- clutch cable
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- 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
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
- C08L23/0869—Acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
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- 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
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Braking Arrangements (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Mechanical Operated Clutches (AREA)
Abstract
The invention discloses a clutch cable joint and a preparation method thereof. The preparation method comprises the following steps: 1) sweet potatoes are crushed and placed in a yeast solution for fermentation, filtering is carried out for preparing a filter cake, and a modifier is obtained; 2) bentonite and iron-ore slag are calcined, an activation treatment is carried out with existence of X-ray, in order to prepare an activator; 3) polycarbonate, an ethene-ethyl acrylate copolymer, cellulose triacetate, ethyl orthosilicate, 1-butanol, nanometer magnesium oxide, rare earth oxide, potassium titanate whiskers, N,N-dimethyldodecylamine, anilino-methyl-triethoxysilane, pyrimidine, p-benzoquinone, vinyl phenyl silicone oil, the modifier and the activator are mixed, cooled, molded and granulated, in order to obtain a clutch cable joint material; 4) the clutch cable joint material is fused at 195-205 DEG C, and extrusion moulding is carried out, in order to obtain the clutch cable joint. The clutch cable joint has excellent mechanical properties.
Description
Technical field
The present invention relates to clutch cable joint, particularly, relate to a kind of clutch cable joint and preparation method thereof.
Background technology
Clutch coupling, is commonly called as and does one's utmost son, in the fly wheel casing between engine and wheel box, is fixed on the back plane of flywheel with screw by clutch assembly, is the device engine power of automobile or other power machines is passed in the mode of switch on axletree.In vehicle traveling process, officer can step on as required or release the clutch pedal, and engine and wheel box is temporarily separated and engages gradually, to cut off or to transmit the power that engine inputs to variator.
Clutch cable joint is one of assembly important in clutch coupling, because clutch cable joint ceaselessly works in the use procedure of clutch coupling, and then causes clutch cable joint very easily to rupture.
Summary of the invention
The object of this invention is to provide a kind of clutch cable joint and preparation method thereof, the clutch cable joint obtained by the method has excellent mechanical property.
To achieve these goals, the invention provides a kind of preparation method of clutch cable joint, comprising:
1) Ipomoea batatas is broken, is then placed in yeast soln and ferments, and then crosses leaching filter cake with obtained properties-correcting agent;
2) wilkinite and Iron-ore Slag are calcined, carry out activation treatment under being then placed in the existence of X-ray with obtained activator;
3) by mixing to polycarbonate, ethylene-ethyl acrylate copolymer, cellulosetri-acetate, tetraethoxy, propyl carbinol, nano magnesia, rare earth oxide, potassium titanate crystal whisker, Dodecyl Dimethyl Amine, anilinomethyl triethoxysilane, pyrimidine, para benzoquinone, vinyl phenyl silicone oil, properties-correcting agent and activator, cooling forming, granulation with obtained clutch cable joint material; 4) by the melting at 195-205 DEG C of described clutch cable joint material, then by extrusion moulding with obtained described clutch cable joint.
Invention further provides a kind of clutch cable joint, this clutch cable joint is obtained by the preparation of above-mentioned method.
By technique scheme, preparation method provided by the invention is divided into four steps, and the first step is: Ipomoea batatas is broken, is then placed in yeast soln and ferments, and then crosses leaching filter cake with obtained properties-correcting agent; Second step is: wilkinite and Iron-ore Slag are calcined, and carries out activation treatment with obtained activator under being then placed in the existence of X-ray; 3rd step is: by mixing to polycarbonate, ethylene-ethyl acrylate copolymer, cellulosetri-acetate, tetraethoxy, propyl carbinol, nano magnesia, rare earth oxide, potassium titanate crystal whisker, Dodecyl Dimethyl Amine, anilinomethyl triethoxysilane, pyrimidine, para benzoquinone, vinyl phenyl silicone oil, properties-correcting agent and activator, cooling forming, granulation with obtained clutch cable joint material; 4th step is: by the melting at 195-205 DEG C of described clutch cable joint material, then by extrusion moulding with obtained described clutch cable joint.By the synergy between each step and the synergy between each material, thus the clutch cable joint obtained is made to have excellent mechanical property.
Other features and advantages of the present invention are described in detail in embodiment part subsequently.
Embodiment
Below the specific embodiment of the present invention is described in detail.Should be understood that, embodiment described herein, only for instruction and explanation of the present invention, is not limited to the present invention.
The invention provides a kind of preparation method of clutch cable joint, comprising:
1) Ipomoea batatas is broken, is then placed in yeast soln and ferments, and then crosses leaching filter cake with obtained properties-correcting agent;
2) wilkinite and Iron-ore Slag are calcined, carry out activation treatment under being then placed in the existence of X-ray with obtained activator;
3) by mixing to polycarbonate, ethylene-ethyl acrylate copolymer, cellulosetri-acetate, tetraethoxy, propyl carbinol, nano magnesia, rare earth oxide, potassium titanate crystal whisker, Dodecyl Dimethyl Amine, anilinomethyl triethoxysilane, pyrimidine, para benzoquinone, vinyl phenyl silicone oil, properties-correcting agent and activator, cooling forming, granulation with obtained clutch cable joint material;
4) by the melting at 195-205 DEG C of described clutch cable joint material, then by extrusion moulding with obtained described clutch cable joint.
In step 1 of the present invention) in, the actual conditions of fermentation can be selected in wide scope, but in order to make the clutch cable joint obtained have more excellent mechanical property, preferably, fermentation at least meets the following conditions: leavening temperature is 45-55 DEG C, and the treatment time is 20-30h.
In step 1 of the present invention) in, the consumption of each material can be selected in wide scope, but in order to make the clutch cable joint obtained, there is more excellent mechanical property, preferably, in step 1) in, relative to the described Ipomoea batatas of 100 weight parts, the consumption of described yeast soln is 200-300 weight part, and the concentration of described yeast soln is 22-30 % by weight.
In step 2 of the present invention) in, the consumption of each material can be selected in wide scope, but in order to make the clutch cable joint obtained, there is more excellent mechanical property, preferably, in step 2) in, relative to the wilkinite of 100 weight parts, the consumption of Iron-ore Slag is 14-23 weight part.
In step 2 of the present invention) in, calcination condition can be selected in wide scope, but in order to make the clutch cable joint obtained have more excellent mechanical property, preferably, calcining at least meets the following conditions: calcining temperature is 440-460 DEG C, and calcination time is 4-6h.
In step 2 of the present invention) in, the condition of activation treatment can be selected in wide scope, but in order to make the clutch cable joint obtained, there is more excellent mechanical property, preferably, in step 2) in, activation treatment at least meets the following conditions: activation temperature is 85-95 DEG C, and soak time is the wavelength of 40-60min, X-ray is 3-5nm.
In step 3 of the present invention) in, the consumption of each material can be selected in wide scope, but in order to make the clutch cable joint obtained, there is more excellent mechanical property, preferably, in step 3) in, relative to the polycarbonate of 100 weight parts, the consumption of ethylene-ethyl acrylate copolymer is 90-110 weight part, the consumption of cellulosetri-acetate is 4-7 weight part, the consumption of tetraethoxy is 16-21 weight part, the consumption of propyl carbinol is 25-33 weight part, the consumption of nano magnesia is 11-17 weight part, the consumption of rare earth oxide is 8-12 weight part, the consumption of potassium titanate crystal whisker is 3-6 weight part, the consumption of Dodecyl Dimethyl Amine is 24-33 weight part, the consumption of anilinomethyl triethoxysilane is 17-27 weight part, the consumption of pyrimidine is 6-13 weight part, the consumption of para benzoquinone is 14-19 weight part, the consumption of vinyl phenyl silicone oil is 2-8 weight part, the consumption of properties-correcting agent is 14-21 weight part, the consumption of activator is 10-16 weight part.
In step 3 of the present invention) in, polycarbonate, ethylene-ethyl acrylate copolymer, the concrete kind of nano magnesia and rare earth oxide can be selected in wide scope, but in order to make the clutch cable joint obtained, there is more excellent mechanical property, preferably, in step 3) in, the weight-average molecular weight of polycarbonate is 4500-7000, the weight-average molecular weight of ethylene-ethyl acrylate copolymer is 8000-12000, the particle diameter of nano magnesia is 8-15nm, rare earth oxide is selected from cerium oxide, europium sesquioxide, one or more in gadolinium sesquioxide and dysprosium oxide.
In step 3 of the present invention) in, condition that is mixing and cooling forming can be selected in wide scope, but in order to make the clutch cable joint obtained, there is more excellent mechanical property, preferably, in step 3) in, mixingly at least to meet the following conditions: melting temperature is 225-230 DEG C, and mixing time is 50-70min; The temperature of cooling forming is 25-30 DEG C.
Invention further provides a kind of clutch cable joint, this clutch cable joint is obtained by the preparation of above-mentioned method.
Below will be described the present invention by embodiment.
Embodiment 1
1) Ipomoea batatas is broken, and the yeast soln (concentration is 25 % by weight) being then placed in 50 DEG C carries out fermentation 28h, then crosses leaching filter cake with obtained properties-correcting agent; Wherein, the weight ratio of Ipomoea batatas and yeast soln is 100:270;
2) wilkinite, Iron-ore Slag are carried out calcining 5h at being incorporated in 450 DEG C according to the weight ratio of 100:20 is mixed, under being then placed in the existence of X-ray (wavelength is 4nm), at 90 DEG C, carry out activation treatment 50min with obtained activator;
3) by polycarbonate (weight-average molecular weight is 6000), ethylene-ethyl acrylate copolymer (weight-average molecular weight is 10000), cellulosetri-acetate, tetraethoxy, propyl carbinol, nano magnesia (particle diameter is 10nm), rare earth oxide (cerium oxide), potassium titanate crystal whisker, Dodecyl Dimethyl Amine, anilinomethyl triethoxysilane, pyrimidine, para benzoquinone, vinyl phenyl silicone oil, properties-correcting agent and activator are according to weight ratio mixing 60min at 228 DEG C of 100:105:5:18:28:15:10:4:29:20:8:17:6:16:13, cooling forming at 29 DEG C, granulation is with obtained clutch cable joint material,
4) by the melting at 200 DEG C of described clutch cable joint material, then by extrusion moulding with obtained described clutch cable joint A1.
Embodiment 2
1) Ipomoea batatas is broken, and the yeast soln (concentration is 22 % by weight) being then placed in 45 DEG C carries out fermentation 20h, then crosses leaching filter cake with obtained properties-correcting agent; Wherein, the weight ratio of Ipomoea batatas and yeast soln is 100:200;
2) wilkinite, Iron-ore Slag are carried out calcining 4h at being incorporated in 440 DEG C according to the weight ratio of 100:14 is mixed, under being then placed in the existence of X-ray (wavelength is 3nm), at 85 DEG C, carry out activation treatment 40min with obtained activator;
3) by polycarbonate (weight-average molecular weight is 4500), ethylene-ethyl acrylate copolymer (weight-average molecular weight is 8000), cellulosetri-acetate, tetraethoxy, propyl carbinol, nano magnesia (particle diameter is 8nm), rare earth oxide (europium sesquioxide), potassium titanate crystal whisker, Dodecyl Dimethyl Amine, anilinomethyl triethoxysilane, pyrimidine, para benzoquinone, vinyl phenyl silicone oil, properties-correcting agent and activator are according to weight ratio mixing 50min at 225 DEG C of 100:90:4:16:25:11:8:3:24:17:6:14:2:14:10, cooling forming at 25 DEG C, granulation is with obtained clutch cable joint material,
4) by the melting at 195 DEG C of described clutch cable joint material, then by extrusion moulding with obtained described clutch cable joint A2.
Embodiment 3
1) Ipomoea batatas is broken, and the yeast soln (concentration is 30 % by weight) being then placed in 55 DEG C carries out fermentation 30h, then crosses leaching filter cake with obtained properties-correcting agent; Wherein, the weight ratio of Ipomoea batatas and yeast soln is 100:300;
2) wilkinite, Iron-ore Slag are carried out calcining 6h at being incorporated in 460 DEG C according to the weight ratio of 100:23 is mixed, under being then placed in the existence of X-ray (wavelength is 5nm), at 95 DEG C, carry out activation treatment 60min with obtained activator;
3) by polycarbonate (weight-average molecular weight is 7000), ethylene-ethyl acrylate copolymer (weight-average molecular weight is 12000), cellulosetri-acetate, tetraethoxy, propyl carbinol, nano magnesia (particle diameter is 15nm), rare earth oxide (dysprosium oxide), potassium titanate crystal whisker, Dodecyl Dimethyl Amine, anilinomethyl triethoxysilane, pyrimidine, para benzoquinone, vinyl phenyl silicone oil, properties-correcting agent and activator are according to weight ratio mixing 70min at 230 DEG C of 100:110:7:21:33:17:12:6:33:27:13:19:8:21:16, cooling forming at 30 DEG C, granulation is with obtained clutch cable joint material,
4) by the melting at 205 DEG C of described clutch cable joint material, then by extrusion moulding with obtained described clutch cable joint A3.
Comparative example 1
Carry out obtained clutch cable joint B1 according to the method for embodiment 1, unlike, step 3) in do not use properties-correcting agent.
Comparative example 2
Carry out obtained clutch cable joint B2 according to the method for embodiment 1, unlike, step 3) in do not use activator.
Test example 1
Carry out tensile strength to above-mentioned clutch cable joint and tear strength detects, concrete outcome is in table 1.
Table 1
| Tensile strength (MPa) | Tear strength (KN/m) | |
| A1 | 66 | 47 |
| A2 | 59 | 51 |
| A3 | 61 | 49 |
| B1 | 31 | 32 |
| B2 | 25 | 30 |
Known by above-described embodiment, comparative example and test example, clutch cable joint provided by the invention has excellent tensile strength and tear strength.
More than describe the preferred embodiment of the present invention in detail; but the present invention is not limited to the detail in above-mentioned embodiment, within the scope of technical conceive of the present invention; can carry out multiple simple variant to technical scheme of the present invention, these simple variant all belong to protection scope of the present invention.
It should be noted that in addition, each concrete technical characteristic described in above-mentioned embodiment, in reconcilable situation, can be combined by any suitable mode, in order to avoid unnecessary repetition, the present invention illustrates no longer separately to various possible array mode.
In addition, also can carry out arbitrary combination between various different embodiment of the present invention, as long as it is without prejudice to thought of the present invention, it should be considered as content disclosed in this invention equally.
Claims (10)
1. a preparation method for clutch cable joint, is characterized in that, comprising:
1) Ipomoea batatas is broken, be then placed in yeast soln and ferment, then cross leaching filter cake with obtained properties-correcting agent;
2) wilkinite and Iron-ore Slag are calcined, carry out activation treatment under being then placed in the existence of X-ray with obtained activator;
3) by polycarbonate, ethylene-ethyl acrylate copolymer, cellulosetri-acetate, tetraethoxy, propyl carbinol, nano magnesia, rare earth oxide, potassium titanate crystal whisker, Dodecyl Dimethyl Amine, anilinomethyl triethoxysilane, pyrimidine, para benzoquinone, vinyl phenyl silicone oil, described properties-correcting agent and activator is mixing, cooling forming, granulation is with obtained clutch cable joint material;
4) by the melting at 195-205 DEG C of described clutch cable joint material, then by extrusion moulding with obtained described clutch cable joint.
2. preparation method according to claim 1, wherein, in step 1) in, described fermentation at least meets the following conditions: leavening temperature is 45-55 DEG C, and the treatment time is 20-30h.
3. preparation method according to claim 1 and 2, wherein, in step 1) in, relative to the described Ipomoea batatas of 100 weight parts, the consumption of described yeast soln is 200-300 weight part, and the concentration of described yeast soln is 22-30 % by weight.
4. preparation method according to claim 3, wherein, in step 2) in, relative to the described wilkinite of 100 weight parts, the consumption of described Iron-ore Slag is 14-23 weight part.
5. preparation method according to claim 4, wherein, in step 2) in, described calcining at least meets the following conditions: calcining temperature is 440-460 DEG C, and calcination time is 4-6h.
6. preparation method according to claim 4, wherein, in step 2) in, described activation treatment at least meets the following conditions: activation temperature is 85-95 DEG C, and soak time is the wavelength of 40-60min, X-ray is 3-5nm.
7. according to the preparation method in claim 4-6 described in any one, wherein, in step 3) in, relative to the described polycarbonate of 100 weight parts, the consumption of described ethylene-ethyl acrylate copolymer is 90-110 weight part, the consumption of described cellulosetri-acetate is 4-7 weight part, the consumption of described tetraethoxy is 16-21 weight part, the consumption of described propyl carbinol is 25-33 weight part, the consumption of described nano magnesia is 11-17 weight part, the consumption of described rare earth oxide is 8-12 weight part, the consumption of described potassium titanate crystal whisker is 3-6 weight part, the consumption of described Dodecyl Dimethyl Amine is 24-33 weight part, the consumption of described anilinomethyl triethoxysilane is 17-27 weight part, the consumption of described pyrimidine is 6-13 weight part, the consumption of described para benzoquinone is 14-19 weight part, the consumption of described vinyl phenyl silicone oil is 2-8 weight part, the consumption of described properties-correcting agent is 14-21 weight part, the consumption of described activator is 10-16 weight part.
8. preparation method according to claim 7, wherein, in step 3) in, the weight-average molecular weight of described polycarbonate is 4500-7000, the weight-average molecular weight of described ethylene-ethyl acrylate copolymer is 8000-12000, the particle diameter of described nano magnesia is 8-15nm, described rare earth oxide be selected from cerium oxide, europium sesquioxide, gadolinium sesquioxide and dysprosium oxide one or more.
9. preparation method according to claim 7, wherein, in step 3) in, describedly mixingly at least to meet the following conditions: melting temperature is 225-230 DEG C, and mixing time is 50-70min; The temperature of described cooling forming is 25-30 DEG C.
10. a clutch cable joint, is characterized in that, described clutch cable joint is obtained by the method preparation in claim 1-9 described in any one.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510976296.5A CN105440427A (en) | 2015-12-22 | 2015-12-22 | Clutch cable joint and preparation method thereof |
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| Application Number | Priority Date | Filing Date | Title |
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| CN201510976296.5A CN105440427A (en) | 2015-12-22 | 2015-12-22 | Clutch cable joint and preparation method thereof |
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| CN105440427A true CN105440427A (en) | 2016-03-30 |
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| CN201510976296.5A Pending CN105440427A (en) | 2015-12-22 | 2015-12-22 | Clutch cable joint and preparation method thereof |
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1451027A (en) * | 2000-01-11 | 2003-10-22 | E·喀硕吉工业有限公司 | Thermoplastic starch compositions in corporating a particulate filler component |
| CN101160356A (en) * | 2005-04-14 | 2008-04-09 | 通用电气公司 | Thermoplastic blends and articles made therefrom |
| CN102020822A (en) * | 2009-09-09 | 2011-04-20 | 第一毛织株式会社 | Molded product assembly |
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2015
- 2015-12-22 CN CN201510976296.5A patent/CN105440427A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1451027A (en) * | 2000-01-11 | 2003-10-22 | E·喀硕吉工业有限公司 | Thermoplastic starch compositions in corporating a particulate filler component |
| CN101160356A (en) * | 2005-04-14 | 2008-04-09 | 通用电气公司 | Thermoplastic blends and articles made therefrom |
| CN102020822A (en) * | 2009-09-09 | 2011-04-20 | 第一毛织株式会社 | Molded product assembly |
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Application publication date: 20160330 |