CN105440247A - High elasticity intake manifold resonant cavity - Google Patents

High elasticity intake manifold resonant cavity Download PDF

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Publication number
CN105440247A
CN105440247A CN201510903117.5A CN201510903117A CN105440247A CN 105440247 A CN105440247 A CN 105440247A CN 201510903117 A CN201510903117 A CN 201510903117A CN 105440247 A CN105440247 A CN 105440247A
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CN
China
Prior art keywords
intake manifold
resonator cavity
gas rail
polyurethane elastomer
snappiness
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Withdrawn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
CN201510903117.5A
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Chinese (zh)
Inventor
李姗姗
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Qingdao Bolaimosi New Material Technology Co Ltd
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Qingdao Bolaimosi New Material Technology Co Ltd
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Priority to CN201510903117.5A priority Critical patent/CN105440247A/en
Publication of CN105440247A publication Critical patent/CN105440247A/en
Withdrawn legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67Unsaturated compounds having active hydrogen
    • C08G18/69Polymers of conjugated dienes
    • C08G18/698Mixtures with compounds of group C08G18/40
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3203Polyhydroxy compounds
    • C08G18/3206Polyhydroxy compounds aliphatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/38Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3802Low-molecular-weight compounds having heteroatoms other than oxygen having halogens
    • C08G18/3804Polyhydroxy compounds
    • C08G18/3806Polyhydroxy compounds having chlorine and/or bromine atoms
    • C08G18/3808Polyhydroxy compounds having chlorine and/or bromine atoms having chlorine atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/4009Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
    • C08G18/4018Mixtures of compounds of group C08G18/42 with compounds of group C08G18/48
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6603Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6607Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
    • C08G18/6611Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203 having at least three hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6603Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6614Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38
    • C08G18/6618Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3225 or polyamines of C08G18/38

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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)
  • Polyurethanes Or Polyureas (AREA)

Abstract

The invention provides a high elasticity intake manifold resonant cavity made of a polyurethane elastomer. The polyurethane elastomer comprises polytetrahydrofuran diol, polycaprolactone diol, hydroxyl-terminated butadiene-arylonitrile rubber, hydroxyl-terminated polybutadiene, Isonal curing agent, TMP, 1,3,5-tris(2-hydroxyethyl)cyanuric acid, toluene diisocyanate, MOCA and dibutyltin dilaurate. The high elasticity intake manifold resonant cavity is made of the polyurethane elastomer, the flex times are as high as more than 200000 times, and the reliability and service life of a whole device are further improved.

Description

A kind of snappiness intake manifold resonator cavity
Technical field
The present invention relates to auto parts machinery field, particularly a kind of intake manifold resonator cavity.
Background technology
In China, the development of automobile industry and plastic manufacturing process is advanced by leaps and bounds, the engine fittings that metal makes are replaced by the engine fittings of the plastic production taking intake manifold as representative gradually, as one of the parts of engine most critical, intake manifold achieves in automobile industry and applies widely, its Core Feature is for each cylinder of engine provides full and uniform gas mixture, is the key factor affecting engine forces and oil consumption.
Motor intake manifold inlet mouth air throttle needs good flexural property, to adapt to the oil-gas jetting of high strength, also directly determines the work-ing life of motor intake manifold entirety its work-ing life.
Therefore, how to replace existing metal to make intake manifold resonator cavity with suitable plastic material, be current problem demanding prompt solution.
Summary of the invention
For solving above-mentioned the deficiencies in the prior art, the present invention proposes a kind of snappiness intake manifold resonator cavity.
Technical scheme of the present invention is achieved in that
A kind of snappiness intake manifold resonator cavity, each intake manifold arm 3 upper end air throttle 1 is communicated with intake manifold resonator cavity 2, each air outlet, intake manifold arm 3 bottom is connected with each cylinder head respectively by joint flange 4, also comprise gas rail 5 and multiple gas rail connecting branch 6, gas rail connecting branch 6 and intake manifold arm 3 one_to_one corresponding, gas rail 5 is communicated with the lower end of each intake manifold arm 3 by gas rail connecting branch 6;
Described intake manifold resonator cavity is made up of polyurethane elastomer, this polyurethane elastomer contains following component and weight part: PTMG dibasic alcohol (PTMG), poly-own Inner ester dibasic alcohol (PCL), terminal hydroxy group nitrile rubber, hydroxy-terminated polybutadienes, Isonal solidifying agent, TMP, Sai Ke, tolylene diisocyanate (TDI-100), 3, chloro-4, the 4-diaminodiphenyl-methanes (MOCA) of 3-bis-, dibutyl tin laurate (T-12).
Alternatively, the processing mode of described polyurethane elastomer is casting type.
Alternatively, described PTMG dibasic alcohol, hydroxyl value 107 ~ 118mgKOH/g.
Alternatively, described tolylene diisocyanate, purity is greater than 99.5%.
The invention has the beneficial effects as follows:
(1) have good physics, chemical property, dielectric properties are good;
(2) intake manifold resonator cavity subdue number of times up to more than 20 ten thousand times, improve further reliability and the work-ing life of Whole Equipment.
Accompanying drawing explanation
In order to be illustrated more clearly in the embodiment of the present invention or technical scheme of the prior art, be briefly described to the accompanying drawing used required in embodiment or description of the prior art below, apparently, accompanying drawing in the following describes is only some embodiments of the present invention, for those of ordinary skill in the art, under the prerequisite not paying creative work, other accompanying drawing can also be obtained according to these accompanying drawings.
Fig. 1 is the Facad structure schematic diagram of the motor intake manifold adopting resonator cavity of the present invention.
Embodiment
Below in conjunction with the accompanying drawing in the embodiment of the present invention, be clearly and completely described the technical scheme in the embodiment of the present invention, obviously, described embodiment is only the present invention's part embodiment, instead of whole embodiments.Based on the embodiment in the present invention, those of ordinary skill in the art, not making the every other embodiment obtained under creative work prerequisite, belong to the scope of protection of the invention.
As shown in Figure 1, adopt the motor intake manifold of resonator cavity of the present invention, comprise intake manifold resonator cavity 1, intake manifold resonator cavity 2, multiple intake manifold arm 3 and joint flange 4, each intake manifold arm 3 upper end air throttle 1 is communicated with intake manifold resonator cavity 2, each air outlet, intake manifold arm 3 bottom is connected with each cylinder head respectively by joint flange 4, also comprise gas rail 5 and multiple gas rail connecting branch 6, gas rail connecting branch 6 and intake manifold arm 3 one_to_one corresponding, gas rail 5 is communicated with the lower end of each intake manifold arm 3 by gas rail connecting branch 6.
Described resonator cavity 2 is made up of polyurethane elastomer, this polyurethane elastomer contains following component and weight part: PTMG dibasic alcohol (PTMG), poly-own Inner ester dibasic alcohol (PCL), terminal hydroxy group nitrile rubber, hydroxy-terminated polybutadienes, Isonal solidifying agent, TMP, Sai Ke, tolylene diisocyanate (TDI-100), 3, chloro-4, the 4-diaminodiphenyl-methanes (MOCA) of 3-bis-, dibutyl tin laurate (T-12).
PTMG dibasic alcohol (PTMG)
White waxy solid, can become transparent liquid when temperature exceedes room temperature.Soluble in alcohol, ester, ketone, aromatic hydrocarbons and chlorinated hydrocarbon, be insoluble to aliphatic hydrocarbon and water.When molecular weight increases, solubleness can reduce.At room temperature, PTMG has water-absorbent.Its water-absorbent depends on the size of molecular weight, the moisture of Absorbable rod 2% time the highest.
PTMG dibasic alcohol of the present invention, hydroxyl value 107 ~ 118mgKOH/g.
Tolylene diisocyanate (TDI-100)
Tolylene diisocyanate be water white transparency to weak yellow liquid, irritant smell; Chance light color deepens.Molecular formula C9-H6-N2-O2.Molecular weight 174.16.Relative density 1.22 ± 0.01 (25 DEG C).3.5 ~ 5.5 DEG C, zero pour (TDI-65); 11.5 ~ 13.5 DEG C (TDI-80); 19.5 ~ 21.5 DEG C.Boiling point 251 DEG C.Flash-point 132 DEG C.Vapour density 6.0.Vapour pressure 0.13kPa (0.01mmHg20 DEG C).Steam and the flammable limit 0.9 ~ 9.5% of air mixture.Water insoluble; Be dissolved in acetone, ethyl acetate and toluene etc.Easily with the compound including reactive hydrogen atom: amine, water, alcohol, acid, alkali react, and are particularly difficult to sodium hydroxide and tertiary amine control to react, and release large calorimetric.React with water that to generate carbonic acid gas be one of committed step in urethane foam manufacturing processed.
Preferably, described tolylene diisocyanate (TDI-100), purity is greater than 99.5%.
Other synthesize component: poly-own Inner ester dibasic alcohol (PCL), hydroxy'terminated butadiene nitrile rubber, hydroxy-terminated polybutadienes, Isonal solidifying agent, TMP, Sai Ke, 3,3-bis-chloro-4,4-diaminodiphenyl-methane (MOCA), dibutyl tin laurate (T-12), be marketable material.
Below in conjunction with specific embodiment, set forth the present invention further.The experimental technique of unreceipted actual conditions in the following example, measures according to national standard usually.If there is no corresponding national standard, then according to general international standard, normal condition or carry out according to the condition that manufacturer advises.Unless otherwise indicated, otherwise all numbers are weight part, and all per-cent is weight percentage, and described polymericular weight is number-average molecular weight.
Unless otherwise defined or described herein, all specialties used herein and scientific words and those skilled in the art the same meaning be familiar with.In addition any method similar or impartial to described content and material all can be applicable in the inventive method.
The synthesis process of polyurethane elastomer is as follows:
To have agitator, thermometer, vacuum interface 500ml there-necked flask in add quantitative polyvalent alcohol, be warming up to 100 ~ 110 DEG C, vacuum hydro-extraction 2.5h (to quality mark in polyvalent alcohol lower than 0.01%), stops after being then cooled to 50 ~ 60 DEG C vacuumizing; Add the TDI-100 measured, rapid stirring, after temperature-stable, slowly heat up and control to be 80 ~ 85 DEG C, after question response is complete, vacuum outgas 0.5h, sealing is preserved stand-by; Take quantitative polyurethane prepolymer, then add appropriate solidifying agent, and add a little T-12 catalyzer, the mould of falling people after stirring rapidly, matched moulds immediately after gelatin phenomenon to appear.Shaping 1h is reacted at 10MPa pressure 120 DEG C; Test piece after the demoulding is constant temperature 10h in the baking oven of 100 DEG C, parks 5d after taking-up, can cut-parts test.
The mechanical property of polyurethane elastomer: 1. determine that-NCO content is 6%, solidify with MOCA, the proportioning changing polyvalent alcohol PTMG and PCL studies their impacts on Mechanical Properties of Polyurethane Elastomers: when the increase of PCL content, intermolecular mutual attractive force becomes large relatively, the hydrogen bond formed between ester group with hard section carbamate groups is relative to be increased, hard section ordered structure is caused also to increase, the increase such as tensile strength, tear strength.2. determine that-NCO content is 6%, change the proportioning of MOCA and ISONAL and study their impacts on Mechanical Properties of Polyurethane Elastomers: the tensile strength of polyurethane elastomer and tear strength increase with the increase of MOCA content.3.-NCO content is 6%, PTMG: terminal hydroxy group nitrile rubber=8:2, when changing proportioning (MOCA:ISONAL=1:3,1:1,3:1) of chainextender MOCA:ISONAL, observe material to subdue and compression heat generation situation: along with the increase of chainextender MOCA ratio, polyurethane elastomer is subdued number of times and obviously reduced.4.-NCO content is 6%, and chainextender consumption is certain, changes polyvalent alcohol proportioning, observes material and subdues situation: along with the increase of PCL ratio, and polyurethane elastomer flexural property also becomes large thereupon.As PTMG:PCL=8:2, subdue number of times up to more than 20 ten thousand times.
Snappiness intake manifold resonator cavity of the present invention adopts polyurethane elastomer to make, and has good physics, chemical property, subdues number of times up to more than 20 ten thousand times, improves the reliability of overall equipment further.
The foregoing is only preferred embodiment of the present invention, not in order to limit the present invention, within the spirit and principles in the present invention all, any amendment done, equivalent replacement, improvement etc., all should be included within protection scope of the present invention.

Claims (4)

1. a snappiness intake manifold resonator cavity, each intake manifold arm (3) upper end air throttle (1) is communicated with intake manifold resonator cavity (2), each intake manifold arm (3) air outlet, bottom is connected with each cylinder head respectively by joint flange (4), also comprise gas rail (5) and multiple gas rail connecting branch (6), gas rail connecting branch (6) and intake manifold arm (3) one_to_one corresponding, gas rail (5) is communicated with by the lower end of gas rail connecting branch (6) with each intake manifold arm (3); It is characterized in that,
Described intake manifold resonator cavity is made up of polyurethane elastomer, this polyurethane elastomer contains following component and weight part: PTMG dibasic alcohol (PTMG), poly-own Inner ester dibasic alcohol (PCL), terminal hydroxy group nitrile rubber, hydroxy-terminated polybutadienes, Isonal solidifying agent, TMP, Sai Ke, tolylene diisocyanate (TDI-100), 3, chloro-4, the 4-diaminodiphenyl-methanes (MOCA) of 3-bis-, dibutyl tin laurate (T-12).
2. snappiness intake manifold resonator cavity according to claim 1, it is characterized in that, its processing mode is casting type.
3. snappiness intake manifold resonator cavity according to claim 1, is characterized in that, described PTMG dibasic alcohol, hydroxyl value 107 ~ 118mgKOH/g.
4. snappiness intake manifold resonator cavity according to claim 1, it is characterized in that, described tolylene diisocyanate, purity is greater than 99.5%.
CN201510903117.5A 2015-12-09 2015-12-09 High elasticity intake manifold resonant cavity Withdrawn CN105440247A (en)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102678402A (en) * 2012-05-28 2012-09-19 奇瑞汽车股份有限公司 Air intake manifold with integrated air track
CN103012736A (en) * 2012-12-10 2013-04-03 青岛宝丽曼高分子材料研究院有限公司 Polyurethane elastomer
CN105418876A (en) * 2015-11-30 2016-03-23 青岛盛嘉信息科技有限公司 High-elasticity engine intake manifold

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102678402A (en) * 2012-05-28 2012-09-19 奇瑞汽车股份有限公司 Air intake manifold with integrated air track
CN103012736A (en) * 2012-12-10 2013-04-03 青岛宝丽曼高分子材料研究院有限公司 Polyurethane elastomer
CN105418876A (en) * 2015-11-30 2016-03-23 青岛盛嘉信息科技有限公司 High-elasticity engine intake manifold

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Application publication date: 20160330