CN107987425A - It is a kind of improve it is polychloroethylene blended when interface bond strength method - Google Patents

It is a kind of improve it is polychloroethylene blended when interface bond strength method Download PDF

Info

Publication number
CN107987425A
CN107987425A CN201711377428.8A CN201711377428A CN107987425A CN 107987425 A CN107987425 A CN 107987425A CN 201711377428 A CN201711377428 A CN 201711377428A CN 107987425 A CN107987425 A CN 107987425A
Authority
CN
China
Prior art keywords
soybean oil
epoxidized soybean
stirring
bond strength
pretreatment
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.)
Withdrawn
Application number
CN201711377428.8A
Other languages
Chinese (zh)
Inventor
肖独山
李毅
邓士武
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anhui Hwasu Corp
Original Assignee
Anhui Hwasu Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Anhui Hwasu Corp filed Critical Anhui Hwasu Corp
Priority to CN201711377428.8A priority Critical patent/CN107987425A/en
Publication of CN107987425A publication Critical patent/CN107987425A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/18Applications used for pipes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention discloses a kind of method of raising interface bond strength when polychloroethylene blended, include the following steps:By polyvinyl chloride, butadiene-styrene rubber, kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay, butyl titanate, tert-butyl hydroperoxide, zinc oxide, magnesia, oxidized polyethylene wax, tributyl 2-acetylcitrate, antioxidant high-temperature stirring, cooling continues stirring and obtains premix;Pretreatment epoxidized soybean oil high-temperature stirring is added into premix, cooling, is sent into mill slice in two-roll mill, compressing to obtain igelite.Epoxidized soybean oil is pre-processed to prepare using following technique:Epoxidized soybean oil, methacrylic acid are uniformly mixed, add triphenylphosphine, heating stirring, cooling, adds nbr carboxyl terminal and stir evenly, and ultraviolet light cures to obtain pretreatment epoxidized soybean oil.The present invention is easy to operate, improves and scattered, storeroom interface bond strength height is blended in igelite.

Description

It is a kind of improve it is polychloroethylene blended when interface bond strength method
Technical field
The present invention relates to polyvinyl chloride technical field, more particularly to a kind of interface bond strength when improving polychloroethylene blended Method.
Background technology
Although PVC material intensity is higher but the problem of generally existing brittleness is larger, its application is have impact on, to make up it not Foot, usually adds toughener to greatly improve the toughness of PVC material in formula, but the use of toughener can reduce the strong of material Degree, vicat softening temperature, to solve the problems, such as this, nanometer particle is applied in PVC material, but since nanometer particle is easily rolled into a ball It is poly-, again there are the problem of poor dispersion and poor interface cohesion when polymer is blended, so as to have impact on the activeness and quietness of PVC material.
The content of the invention
Based on technical problem existing for background technology, the present invention proposes a kind of interface cohesion when improving polychloroethylene blended The method of intensity, it is easy to operate, improve and scattered, storeroom interface bond strength height, gained polychlorostyrene are blended in igelite Vinyl plastics good fluidity, density is big, and heat endurance is good, and crosslinking degree is high, effectively increases intensity and vicat softening temperature.
It is proposed by the present invention it is a kind of improve it is polychloroethylene blended when interface bond strength method, include the following steps:
S1, by polyvinyl chloride, butadiene-styrene rubber, kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay, four fourth of metatitanic acid Ester, tert-butyl hydroperoxide, zinc oxide, magnesia, oxidized polyethylene wax, tributyl 2-acetylcitrate, antioxidant high-temperature stirring, Cooling continues stirring and obtains premix;
S2, add pretreatment epoxidized soybean oil high-temperature stirring into premix, and cooling, is sent into mill in two-roll mill and goes out Piece, it is compressing to obtain igelite.
Preferably, in S1, polyvinyl chloride, butadiene-styrene rubber, kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay, titanium Sour four butyl esters, tert-butyl hydroperoxide, zinc oxide, magnesia, oxidized polyethylene wax, tributyl 2-acetylcitrate, antioxidant Weight ratio is 120-140:30-50:15-25:10-20:6-12:6-12:5-9:1-2:3-5:1-2:0.8-1.6:4-8:4-8: 4-8。
Preferably, in S1, by polyvinyl chloride, butadiene-styrene rubber, kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay, Butyl titanate, tert-butyl hydroperoxide, zinc oxide, magnesia, oxidized polyethylene wax, tributyl 2-acetylcitrate, antioxidant 10-20min, mixing speed 2000-2400r/min are stirred, whipping temp is 125-135 DEG C, is cooled to 55-65 DEG C and continues to stir 20-40min is mixed, obtains premix.
Preferably, in S2, the weight ratio of premix and pretreatment epoxidized soybean oil is 100-130:4-8.
Preferably, in S2, pretreatment epoxidized soybean oil stirring 10-20min is added into premix, mixing speed is 1000-1800r/min, whipping temp are 120-140 DEG C, are cooled to 45-55 DEG C, feeding temperature is 190-200 DEG C of double roller mill Mill slice in machine, it is compressing to obtain igelite.
Preferably, in S2, pretreatment epoxidized soybean oil is prepared using following technique:By epoxidized soybean oil, methacrylic acid It is uniformly mixed, adds triphenylphosphine, heating stirring, cooling, adds nbr carboxyl terminal and stir evenly, ultraviolet light cures to obtain Pre-process epoxidized soybean oil.
Preferably, in the preparation process of the pretreatment epoxidized soybean oil of S2, epoxidized soybean oil, methacrylic acid, triphenyl Phosphine, the weight ratio of nbr carboxyl terminal are 6-12:16-22:0.04-0.08:1-2.
Preferably, in S2, pretreatment epoxidized soybean oil is prepared using following technique:By epoxidized soybean oil, methacrylic acid It is uniformly mixed, adds triphenylphosphine, is warming up to 115-125 DEG C of stirring 40-60min, is cooled to 55-65 DEG C, adds end carboxyl fourth Nitrile rubber stirs evenly, and ultraviolet light cures to obtain pretreatment epoxidized soybean oil.
The apparent density of gained igelite of the invention is high, and dry good fluidity, easily plasticizing, melt rheological property is good, and heat is steady Qualitative height, has larger industrializing implementation prospect.
In the pretreatment epoxidized soybean oil of the present invention, using epoxidized soybean oil as raw material, add under the cooperation of methacrylic acid Enter nbr carboxyl terminal combination, can not only improve the toughening effect of epoxidized soybean oil, but also make to contain substantial amounts of double bond in product, It is active high, it on the one hand can effectively be combined with polyvinyl chloride, butadiene-styrene rubber, form more cross-linked structures, reinforcing material Intensity and vicat softening temperature, on the other hand can promote kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay in polychlorostyrene second Disperse in alkene, mutual degree of scatter is high, and good fluidity, density is big, and heat endurance is good, and storeroom interface bond strength is high, can The additive amount of polyvinyl chloride is effectively reduced, reduces cost, is more advantageous to improving the mechanical property of polyvinyl chloride, while there is operation Simply, industrialized feature is easily realized.
Polychloroethylene pipes obtained by the present invention are tested for the property:Its Mohs' hardness is 20 degree, and breaking strength is more than 17Mpa, elongation at break are more than 255%, and compression ratio is less than 30%;450 DEG C of hot winds bake 2h, its compressive resistance is 240 degree, is resisted It is 65 degree to roll over intensity, wear extent 2.2g/cm3
Embodiment
In the following, technical scheme is described in detail by specific embodiment.
Embodiment 1
It is a kind of improve it is polychloroethylene blended when interface bond strength method, include the following steps:
S1, by 120kg polyvinyl chloride, 50kg butadiene-styrene rubber, 15kg kaolin, 20kg diatomite, 6kg talcum powder, 12kg Vermiculite power, 5kg hard (china) clays, 2kg butyl titanates, 3kg tert-butyl hydroperoxide, 2kg zinc oxide, 0.8kg magnesia, 8kg Oxidized polyethylene wax, 4kg tributyl 2-acetylcitrates, 8kg antioxidants stirring 10min, mixing speed 2400r/min, stirring Temperature is 125 DEG C, is cooled to 65 DEG C and continues to stir 20min, obtains premix;
S2, add 4kg pretreatment epoxidized soybean oil stirrings 20min, mixing speed 1000r/ into 130kg premixes Min, whipping temp are 140 DEG C, are cooled to 45 DEG C, are sent into temperature as mill slice in 200 DEG C of two-roll mills, compressing To igelite.
Epoxidized soybean oil is pre-processed to prepare using following technique:6kg epoxidized soybean oils, 22kg methacrylic acids are mixed equal It is even, 0.04kg triphenylphosphines are added, 125 DEG C of stirring 40min is warming up to, is cooled to 65 DEG C, add 1kg nbr carboxyl terminals and stir Mix uniformly, ultraviolet light cures to obtain pretreatment epoxidized soybean oil.
Embodiment 2
It is a kind of improve it is polychloroethylene blended when interface bond strength method, include the following steps:
S1, by 140kg polyvinyl chloride, 30kg butadiene-styrene rubber, 25kg kaolin, 10kg diatomite, 12kg talcum powder, 6kg Vermiculite power, 9kg hard (china) clays, 1kg butyl titanates, 5kg tert-butyl hydroperoxide, 1kg zinc oxide, 1.6kg magnesia, 4kg Oxidized polyethylene wax, 8kg tributyl 2-acetylcitrates, 4kg antioxidants stirring 20min, mixing speed 2000r/min, stirring Temperature is 135 DEG C, is cooled to 55 DEG C and continues to stir 40min, obtains premix;
S2, add 8kg pretreatment epoxidized soybean oil stirrings 10min, mixing speed 1800r/ into 100kg premixes Min, whipping temp are 120 DEG C, are cooled to 55 DEG C, are sent into temperature as mill slice in 190 DEG C of two-roll mills, compressing To igelite.
Epoxidized soybean oil is pre-processed to prepare using following technique:12kg epoxidized soybean oils, 16kg methacrylic acids are mixed Uniformly, 0.08kg triphenylphosphines are added, 115 DEG C of stirring 60min is warming up to, is cooled to 55 DEG C, adds 2kg nbr carboxyl terminals Stir evenly, ultraviolet light cures to obtain pretreatment epoxidized soybean oil.
Embodiment 3
It is a kind of improve it is polychloroethylene blended when interface bond strength method, include the following steps:
S1, by 125kg polyvinyl chloride, 45kg butadiene-styrene rubber, 18kg kaolin, 18kg diatomite, 8kg talcum powder, 10kg Vermiculite power, 6kg hard (china) clays, 1.8kg butyl titanates, 3.5kg tert-butyl hydroperoxide, 1.7kg zinc oxide, 1kg magnesia, 7kg oxidized polyethylene wax, 5kg tributyl 2-acetylcitrates, 7kg antioxidants stirring 12min, mixing speed 2300r/min, is stirred Temperature is mixed as 128 DEG C, 62 DEG C is cooled to and continues to stir 25min, obtain premix;
S2, add 5kg pretreatment epoxidized soybean oil stirrings 18min, mixing speed 1200r/ into 120kg premixes Min, whipping temp are 135 DEG C, are cooled to 48 DEG C, are sent into temperature as mill slice in 198 DEG C of two-roll mills, compressing To igelite.
Epoxidized soybean oil is pre-processed to prepare using following technique:8kg epoxidized soybean oils, 20kg methacrylic acids are mixed equal It is even, 0.05kg triphenylphosphines are added, 122 DEG C of stirring 45min is warming up to, is cooled to 62 DEG C, adds 1.2kg nbr carboxyl terminals Stir evenly, ultraviolet light cures to obtain pretreatment epoxidized soybean oil.
Embodiment 4
It is a kind of improve it is polychloroethylene blended when interface bond strength method, include the following steps:
S1, by 135kg polyvinyl chloride, 35kg butadiene-styrene rubber, 22kg kaolin, 12kg diatomite, 10kg talcum powder, 8kg Vermiculite power, 8kg hard (china) clays, 1.2kg butyl titanates, 4.5kg tert-butyl hydroperoxide, 1.3kg zinc oxide, 1.4kg oxidations Magnesium, 5kg oxidized polyethylene wax, 7kg tributyl 2-acetylcitrates, the stirring of 5kg antioxidants 18min, mixing speed 2100r/ Min, whipping temp are 132 DEG C, are cooled to 58 DEG C and continue to stir 35min, obtain premix;
S2, add 7kg pretreatment epoxidized soybean oil stirrings 12min, mixing speed 1600r/ into 110kg premixes Min, whipping temp are 125 DEG C, are cooled to 52 DEG C, are sent into temperature as mill slice in 192 DEG C of two-roll mills, compressing To igelite.
Epoxidized soybean oil is pre-processed to prepare using following technique:10kg epoxidized soybean oils, 18kg methacrylic acids are mixed Uniformly, 0.07kg triphenylphosphines are added, 118 DEG C of stirring 55min is warming up to, is cooled to 58 DEG C, adds 1.8kg end carboxyl butyronitrile rubbers Glue stirs evenly, and ultraviolet light cures to obtain pretreatment epoxidized soybean oil.
The foregoing is only a preferred embodiment of the present invention, but protection scope of the present invention be not limited thereto, Any one skilled in the art the invention discloses technical scope in, technique according to the invention scheme and its Inventive concept is subject to equivalent substitution or change, should be covered by the protection scope of the present invention.

Claims (8)

1. it is a kind of improve it is polychloroethylene blended when interface bond strength method, it is characterised in that include the following steps:
S1, by polyvinyl chloride, butadiene-styrene rubber, kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay, butyl titanate, uncle Butylhydroperoxide, zinc oxide, magnesia, oxidized polyethylene wax, tributyl 2-acetylcitrate, antioxidant high-temperature stirring, cooling Continue stirring and obtain premix;
S2, add pretreatment epoxidized soybean oil high-temperature stirring into premix, and cooling, is sent into mill slice in two-roll mill, It is compressing to obtain igelite.
2. the method for interface bond strength when improving polychloroethylene blended according to claim 1, it is characterised in that in S1, Polyvinyl chloride, butadiene-styrene rubber, kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay, butyl titanate, t-butyl peroxy It is 120-140 to change hydrogen, zinc oxide, magnesia, oxidized polyethylene wax, tributyl 2-acetylcitrate, the weight ratio of antioxidant:30- 50:15-25:10-20:6-12:6-12:5-9:1-2:3-5:1-2:0.8-1.6:4-8:4-8:4-8.
3. it is according to claim 1 or claim 2 improve it is polychloroethylene blended when interface bond strength method, it is characterised in that S1 In, by polyvinyl chloride, butadiene-styrene rubber, kaolin, diatomite, talcum powder, vermiculite power, hard (china) clay, butyl titanate, the tert-butyl group Hydrogen peroxide, zinc oxide, magnesia, oxidized polyethylene wax, tributyl 2-acetylcitrate, antioxidant stirring 10-20min, stirring Speed is 2000-2400r/min, and whipping temp is 125-135 DEG C, is cooled to 55-65 DEG C and continues to stir 20-40min, obtains pre- Batch mixing.
4. the method for interface bond strength, its feature exist when improving polychloroethylene blended according to any one of claim 1-3 is described In in S2, the weight ratio of premix and pretreatment epoxidized soybean oil is 100-130:4-8.
5. the method for interface bond strength, its feature exist when improving polychloroethylene blended according to any one of claim 1-4 is described In, in S2, pretreatment epoxidized soybean oil stirring 10-20min, mixing speed 1000-1800r/min are added into premix, Whipping temp is 120-140 DEG C, is cooled to 45-55 DEG C, is sent into temperature as mill slice in 190-200 DEG C of two-roll mill, pressure The type of being made obtains igelite.
6. the method for interface bond strength, its feature exist when improving polychloroethylene blended according to any one of claim 1-5 is described In in S2, pretreatment epoxidized soybean oil is prepared using following technique:Epoxidized soybean oil, methacrylic acid are uniformly mixed, added Triphenylphosphine, heating stirring, cooling, adds nbr carboxyl terminal and stirs evenly, and it is big that ultraviolet light cures to obtain pretreatment epoxy Soya-bean oil.
7. the method for interface bond strength, its feature exist when improving polychloroethylene blended according to any one of claim 1-6 is described In, in the preparation process of the pretreatment epoxidized soybean oil of S2, epoxidized soybean oil, methacrylic acid, triphenylphosphine, end carboxyl butyronitrile The weight ratio of rubber is 6-12:16-22:0.04-0.08:1-2.
8. the method for interface bond strength, its feature exist when improving polychloroethylene blended according to any one of claim 1-7 is described In in S2, pretreatment epoxidized soybean oil is prepared using following technique:Epoxidized soybean oil, methacrylic acid are uniformly mixed, added Triphenylphosphine, is warming up to 115-125 DEG C of stirring 40-60min, is cooled to 55-65 DEG C, it is equal to add nbr carboxyl terminal stirring Even, ultraviolet light cures to obtain pretreatment epoxidized soybean oil.
CN201711377428.8A 2017-12-19 2017-12-19 It is a kind of improve it is polychloroethylene blended when interface bond strength method Withdrawn CN107987425A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711377428.8A CN107987425A (en) 2017-12-19 2017-12-19 It is a kind of improve it is polychloroethylene blended when interface bond strength method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711377428.8A CN107987425A (en) 2017-12-19 2017-12-19 It is a kind of improve it is polychloroethylene blended when interface bond strength method

Publications (1)

Publication Number Publication Date
CN107987425A true CN107987425A (en) 2018-05-04

Family

ID=62038878

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711377428.8A Withdrawn CN107987425A (en) 2017-12-19 2017-12-19 It is a kind of improve it is polychloroethylene blended when interface bond strength method

Country Status (1)

Country Link
CN (1) CN107987425A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6043318A (en) * 1996-09-27 2000-03-28 Hardiman; Christopher John Nitrile rubber/polyvinyl chloride blends
CN102850696A (en) * 2012-09-20 2013-01-02 吴江市天源塑胶有限公司 High-toughness polyvinyl chloride tube
CN105440483A (en) * 2015-12-10 2016-03-30 安徽宁国市高新管业有限公司 High-toughness corrosion-resistant PVC pipe

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6043318A (en) * 1996-09-27 2000-03-28 Hardiman; Christopher John Nitrile rubber/polyvinyl chloride blends
CN102850696A (en) * 2012-09-20 2013-01-02 吴江市天源塑胶有限公司 High-toughness polyvinyl chloride tube
CN105440483A (en) * 2015-12-10 2016-03-30 安徽宁国市高新管业有限公司 High-toughness corrosion-resistant PVC pipe

Similar Documents

Publication Publication Date Title
CN103992589B (en) A kind of wood plastic building mould utilizing recovery waste material to produce and preparation method thereof
CN103524930A (en) Cold-resistant PVC sheath material for cable and preparation method thereof
CN102898941A (en) Modified nylon powder coating and preparation method thereof
CN107141657A (en) A kind of antistatic co-extrusion wood plastic composite
CN108410091A (en) A kind of PVC heat stabilizer based on polyol ester metal complex
CN112159570A (en) Environment-friendly PVC (polyvinyl chloride) pipe
CN107987425A (en) It is a kind of improve it is polychloroethylene blended when interface bond strength method
CN108250686A (en) A kind of heat conduction high pressure breakdown Electric insulation material and preparation method thereof
CN103289530B (en) A kind of powdery paints of high adhesion force
CN103849139A (en) Low-warp flame-retardant reinforced PA6 engineering plastic, and preparation method thereof
CN104086959A (en) Protein plastic material
CN107955314A (en) A kind of chopped basalt fibre flexibilized polypropylene material and preparation method
CN107057241A (en) A kind of power electric meter erosion resisting insulation sheathing material and preparation method thereof
CN103289515B (en) A kind of ageing-resistant powder coating
CN103483692A (en) Railway signal cable sheathing material
CN104194189A (en) Low-cost gel cable material
CN108948417A (en) A kind of compounding conductive powder, PP composite material and the preparation method and application thereof
CN107189280A (en) A kind of plastic material and preparation method thereof
CN106589744A (en) Environment-friendly plastic and preparation method thereof
CN103613319A (en) Green and environment-friendly plasticizer
CN110092961B (en) High-performance nonpolar rubber material and preparation method thereof
CN103289528A (en) Anti-corrosion powder coating
CN108047553A (en) A kind of polypropylene material of automobile using high impact strength
CN103289526A (en) Powder coating with high water resistance
CN105017687A (en) Cold-resistant and low-temperature-resistant polyvinyl chloride cable material and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication
WW01 Invention patent application withdrawn after publication

Application publication date: 20180504