CN107573989A - A kind of valve derusting lubricant - Google Patents
A kind of valve derusting lubricant Download PDFInfo
- Publication number
- CN107573989A CN107573989A CN201710688403.3A CN201710688403A CN107573989A CN 107573989 A CN107573989 A CN 107573989A CN 201710688403 A CN201710688403 A CN 201710688403A CN 107573989 A CN107573989 A CN 107573989A
- Authority
- CN
- China
- Prior art keywords
- parts
- valve
- added
- lubricant
- mixed
- 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.)
- Pending
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention discloses a kind of valve derusting lubricant, it is related to valve lubrication technical field, there are following raw material components to be made:Isopropyl acetate, laurene, propane diols, dimethicone, mineral oil, honey, hyaluronic acid, down alkene, Tea Polyphenols, modified poly ethylene glycol 8000, lignosulfite, tertiary butyl hydroxyl fennel seeds brain, chaff amine, SAIB, urethane acrylate complex emulsions, duck wheat brass, peanut oil, long-term effect capric acid glyceryl ester zinc oxide, calcium carbonate;It is safe and non-toxic that the present invention prepares valve derusting lubricant material, to environment, pollution-free, does not damage valve, and using late gate derusting, lubricating oil is recyclable re-works utilizations, realizes huge profit saving resource;Part can be got rusty using prevention valve in advance, and lubricate valve working;When part gets rusty, it can be used and remove rusty stain dirt maintenance valve;Prepare valve derusting lubricant it is nontoxic to human body, user can be safe to use.
Description
Technical field:
The present invention relates to valve lubrication technical field, and in particular to a kind of valve derusting lubricant.
Background technology:
Valve is the control unit in fluid delivery system, has cut-off, regulation, water conservancy diversion, prevents adverse current, voltage stabilizing, shunting
Or the function such as overflow pressure relief.For the valve of fluid control systems, from simplest stop valve to extremely complex robot control system(RCS)
In used various valves, its kind and specification are quite various.
Valve can be used for controlling empty gas and water, steam, various Korrosionsmediums, mud, oil product, liquid metal and radioactivity
The flowing of all kinds fluid such as medium.Valve is also divided into cast iron valve according to material, cast steel valve, stainless valve (201,
304th, 316 etc.), chrome-molybdenum steel valve, Chrominm-molybdenum-vanadium steel valve, dual phase steel valve, Plastic valve, nonstandard customized valve etc..
The valve species used in life is various, but contacts use with liquid for a long time, it may appear that some failures, such as:
Gland leakage, closure member leakage, valve rod lifting failure, stem gasket leakage;The appearance of these failures mostly with each portion of valve
Part goes wrong relevant, and as valve gets rusty, impurity pollution, valve fracture etc. all influences the good using effect of valve.
A kind of valve derusting lubricant is developed to this present invention.
The content of the invention:
The technical problems to be solved by the invention are to provide a kind of valve derusting lubricant, safe and non-toxic, best in quality,
Using lasting, lubrication valve, removal rusty stain, prevent from getting rusty.
The technical problems to be solved by the invention are realized using following technical scheme:
A kind of valve derusting lubricant, the raw material components for having following parts by weight are made:
Isopropyl acetate 5-60 parts, laurene 4-50 parts, propane diols 2-34 parts, dimethicone 3-19 parts, mineral oil 2-
59 parts, honey 2-37 parts, hyaluronic acid 3-18 parts, down alkene 3-30 parts, Tea Polyphenols 2-18 parts, modified poly ethylene glycol 80002-23
Part, lignosulfite 2-17 parts, tertiary butyl hydroxyl fennel seeds brain 2-10 parts, chaff amine 3-60 parts, sucrose acetate isobutyric acid
Ester 2-23 parts, polyurethane-acrylate composite emulsion 1-8 parts, duck wheat brass 2-16 parts, peanut oil 3-34 parts, the long-term effect last of the ten Heavenly stems
Sour glyceryl ester-zinc oxide 3-16 parts, calcium carbonate 0.5-2 parts.
The preparation method of modified poly ethylene glycol 8000:Macrogol 8000 is added in reactor, starts stirring,
Quantitative ethanol solution is slowly added to, heated up 60-160 DEG C of addition hydrogen peroxide solution, and 40-80 DEG C is warming up in 20-60min, is protected
Warm 1-5h, decompression dehydration, quantitative boric acid is added, be warming up to 200 DEG C in 20-50min, stir 20-40min, question response thing is opened
During beginning retrogradation, dehydration, 180 DEG C of gelation times release green-yellow thick liquid while hot when being 60-90s, and obtaining denaturation after cooling changes
Property the precursor of macrogol 8000, add in backward precursor in 0.5-2 part silica add 0.3-1.5 parts turpentine oil,
0.5-1 part PDDAs, it is sufficiently mixed after microwave treatment under microwave frequency 2450MHz, power 700W
5-30min, 1-2 parts rilanit special, 0.5-1 parts kayexalate and 0.5-1 part N methyldiethanol amines are added, mixed
Continue microwave treatment 5min after closing uniformly, microwave treatment is transferred to sealing and standing 3h in 0-5 DEG C of environment, then heated immediately after terminating
To 125-130 DEG C of insulation mixing 10-30min, 6-18 0-5 DEG C of cold water of part is added into gained mixture, is stood after being sufficiently mixed
1h, it is subsequently heated to reflux state and is incubated mixing 5-30min, and naturally cool to room temperature, be finally sent into spray dryer, does
Dry gained particle is modified poly ethylene glycol 8000.
The polyurethane-acrylate composite emulsion preparation method:Polyurethane-acrylate is added in deionized water,
60-120 DEG C of heating treats that material is completely dissolved, and bisphenol A type epoxy resin and trimethylolpropane tris propionic acid are added in backward solution
Ester 1000-3000rpm/min, 15-30min is stirred, be prepared into low crosslinking degree nucleocapsid, backward emulsion adds glutaraldehyde, and room temperature is stirred
Mix 10-40min, after place it in refrigerator 0 ± 5 DEG C of placement 12-24H, irradiated after being drawn off, radiation parameter is:
Under Co-60 radiation, 10-20KGy irradiation 1-4h, room temperature is placed after taking-up.
The long-term effect capric acid glyceryl ester-zinc oxide preparation method is:By potassium chlorate, capric acid glyceryl ester, zinc oxide
It is placed in reaction bulb, shake well, after making reactant well mixed, heating, obtained carbon dioxide is dissolved in containing carbon
In sour sodium, hydrogenperoxide steam generator, it is 9-10 to make into PH, and concentration is 4-5% stablizing solution;By stablizing solution and appropriate capric acid
Glyceryl ester, 1.5-3% agar, inorganic filler etc. are well mixed, obtain 1 solidification material components I;Again by hydrochloric acid, capric acid triglycerin
After ester, 1.5-3% agar and inorganic filler are fully adjusted, shape acid releasing agent compositionⅱ must be solidified;Components I and compositionⅱ are mixed afterwards
Close it is uniform, after be put into dryer and dry moisture and be put into 20-30%, then by material in comminutor, nano particle is made and produces
Long-term effect capric acid glyceryl ester-zinc oxide.
Preferably, its preparation method is as follows:
(1) first isopropyl acetate 5-60 parts, laurene 4-50 parts, propane diols 2-34 parts are added in deionized water and heated
40-80 DEG C of heating is sufficiently uniformly dissolved, and dimethicone 3-19 parts, mineral oil 2-59 parts, honey 2-37 are added in backward solution
Part, hyaluronic acid 3-18 parts, are first heated to 80-180 DEG C, it is 1000- that thing to be mixed, which dissolves and is cooled to room temperature in rotating speed,
Grind and stir in 5000rpm/min heating grinder, take out the mixture that 1-12h is dried in 50-120 DEG C of baking oven afterwards
Ⅰ;
(2) by step 1 gained mixture I and down alkene 3-30 parts, Tea Polyphenols 2-18 parts, modified poly ethylene glycol 80002-23
Part, lignosulfite 2-17 parts, tertiary butyl hydroxyl fennel seeds brain 2-10 parts are added in heated at high speed mixing mill,
1000-3000rpm/min is uniformly mixed;
(3) material, which is added in fluid-flywheel clutch, after being well mixed in step 2 is mixed, rear to add in refiner,
Refine repeatedly refines material, so as to obtain valve derusting lubricant matrix;
(4) by the valve obtained in step 3 derusting lubricant matrix and chaff amine 3-60 parts, SAIB 2-
23 parts, polyurethane-acrylate composite emulsion 1-8 parts be heated at high temperature at 30-90 DEG C and homogenizer and be well mixed, in microwave frequency
For microwave treatment 10-30min under 2450MHz, power 800w, material I is produced after well mixed;
(5) by peanut oil 3-34 parts, duck wheat brass 2-16 parts, long-term effect capric acid glyceryl ester-zinc oxide 3-16 parts, plus
Enter into 5 times of 0.1-0.5% mineral oil solutions, being stored at room temperature 1-24h is uniformly dissolved it, in 30-50 DEG C of condition high-speed stirred
Well mixed, rear addition calcium carbonate 0.5-2 parts are microwave treatment 10-30min under 2450MHz, power 800w in microwave frequency, are mixed
Material II is produced after closing uniformly;
(6) material I and material II are mixed, is warming up to 40-60 DEG C and is sufficiently stirred 15-60min, it is rear to stand room temperature again
1000-5000rpm/min 20-40 DEG C insulated and stirred 20-40min, it is rear to stand room temperature cooling, obtain mixing sticky material;Will be mixed
Compound material is added in mulser, is acted on by mulser and is produced valve derusting lubricant.
Valve derusting lubricant application method:When valve each several part stands intact bad when, every 2 weeks, addition derusting lubricates
Agent is maintained, and prevention is got rusty;When valve has rusty stain, addition valve derusting lubricant first derusts decontamination, is cleaned and done with clear water
Only, a small amount of valve derusting lubricant maintenance is added afterwards.
The beneficial effects of the invention are as follows:Prepared by the present invention valve derusting lubricant the selection of material it is safe and non-toxic, to environment,
It is pollution-free, the objects such as valve are not damaged, and being derusted using late gate, lubricating oil is recyclable to re-work utilization, realizes that huge profit is saved
Resource, and this product it is best in quality, using lasting, part can be got rusty using prevention valve in advance, and lubricate valve working;Part is given birth to
During rust, it can be used and remove rusty stain dirt maintenance valve;Prepare valve derusting lubricant it is nontoxic to human body, user, which can trust, to be made
With.
Embodiment:
In order that the technical method that the present invention realizes, creation characteristic, reached purpose are easy to understand with effect, tied below
Specific embodiment is closed, the present invention is expanded on further.
Embodiment 1
A kind of valve derusting lubricant, the raw material components for having following parts by weight are made:
26 parts of isopropyl acetate, 15 parts of laurene, 24 parts of propane diols, 11 parts of dimethicone, 29 parts of mineral oil, honey 27
Part, 13 parts of hyaluronic acid, 10 parts of down alkene, 12 parts of Tea Polyphenols, 800023 parts of modified poly ethylene glycol, 7 parts of lignosulfite,
10 parts of tertiary butyl hydroxyl fennel seeds brain, 20 parts of chaff amine, 9 parts of SAIB, polyurethane-acrylate composite emulsion
6 parts, 11 parts of duck wheat brass, 14 parts of peanut oil, long-term effect capric acid glyceryl ester -6 parts of zinc oxide, 0.5 part of calcium carbonate.
The preparation method of modified poly ethylene glycol 8000:Macrogol 8000 is added in reactor, starts stirring,
Quantitative ethanol solution is slowly added to, heated up 80 DEG C of addition hydrogen peroxide solutions, and 40 DEG C are warming up in 20-60min, 1h is incubated, subtracts
Press-dehydrating, quantitative boric acid is added, be warming up to 200 DEG C in 20min, stir 20min, when question response thing starts retrogradation, dehydration,
180 DEG C of gelation times release green-yellow thick liquid while hot when being 60s, are obtained after cooling before being denatured modified poly ethylene glycol 8000
Body thing, add in backward precursor and 0.3 part of turpentine oil, 0.5 part of poly dimethyl allyl chlorination are added in 0.5 part of silica
Ammonium, be sufficiently mixed after microwave treatment 15min under microwave frequency 2450MHz, power 700W, add 1 part of rilanit special,
0.5 part of kayexalate and 0.5 part of N methyldiethanol amine, continue microwave treatment 5min, microwave treatment after being well mixed
Sealing and standing 3h in 0-5 DEG C of environment is transferred to after end immediately, 125-130 DEG C of insulation mixing 15min is then heated to, is mixed to gained
16 parts of 0-5 DEG C of cold water are added in compound, 1h is stood after being sufficiently mixed, is subsequently heated to reflux state and is incubated mixing 5min, and certainly
Room temperature so is cooled to, is finally sent into spray dryer, it is modified poly ethylene glycol 8000 to dry gained particle.
The polyurethane-acrylate composite emulsion preparation method:Polyurethane-acrylate is added in deionized water,
80 DEG C of heating treats that material is completely dissolved, and bisphenol A type epoxy resin and trimethylolpropane tris propionic ester are added in backward solution
1000rpm/min, 15min being stirred, be prepared into low crosslinking degree nucleocapsid, backward emulsion adds glutaraldehyde, 10min is stirred at room temperature, after
- 5 DEG C of placement 24H in refrigerator are placed it in, are irradiated after being drawn off, radiation parameter is:Under Co-60 radiation, 20KGy spokes
According to 4h, room temperature is placed after taking-up.
The long-term effect capric acid glyceryl ester-zinc oxide preparation method is:By potassium chlorate, capric acid glyceryl ester, zinc oxide
It is placed in reaction bulb, shake well, after making reactant well mixed, heating, obtained carbon dioxide is dissolved in containing carbon
In sour sodium, hydrogenperoxide steam generator, it is 9 to make into PH, and concentration is 4-5% stablizing solution;By stablizing solution and appropriate capric acid three
Glyceride, 1.5-3% agar, inorganic filler etc. are well mixed, obtain 1 solidification material components I;Again by hydrochloric acid, capric acid glyceryl ester,
After 1.5-3% agar and inorganic filler are fully adjusted, shape acid releasing agent compositionⅱ must be solidified;Components I and compositionⅱ are mixed afterwards
Uniformly, drying moisture in dryer is put into after to be put into comminutor in 20-30%, then by material, and nano particle is made and produces length
Effect property capric acid glyceryl ester-zinc oxide.
Preferably, its preparation method is as follows:
(1) 26 parts of isopropyl acetate, 15 parts of laurene, 24 parts of propane diols are first added into 70 DEG C of heating of heating in deionized water
It is sufficiently uniformly dissolved, 11 parts of dimethicone, 29 parts of mineral oil, 27 parts of honey, 14 parts of hyaluronic acid is added in backward solution, first
100 DEG C are heated to, thing to be mixed dissolves and is cooled to room temperature grinds stirring in the heating grinder that rotating speed is 2000rpm/min
Uniformly, the mixture I that 2h is dried in 60 DEG C of baking ovens is taken out afterwards;
(2) by step 1 gained mixture I and 10 parts of down alkene, 12 parts of Tea Polyphenols, 800023 parts of modified poly ethylene glycol, Asia
7 parts of sulphate pulp waste liquid, 10 parts of tertiary butyl hydroxyl fennel seeds brain are added in heated at high speed mixing mill, and 1500rpm/min is stirred
Mix well mixed;
(3) material, which is added in fluid-flywheel clutch, after being well mixed in step 2 is mixed, rear to add in refiner,
Refine repeatedly refines material, so as to obtain valve derusting lubricant matrix;
(4) by the valve obtained in step 3 derust 20 parts of lubricant matrix and chaff amine, 9 parts of SAIB,
6 parts of polyurethane-acrylate composite emulsion is heated at high temperature homogenizers at 60 DEG C and is well mixed, in microwave frequency be 2450MHz,
Microwave treatment 15min under power 800w, material I is produced after well mixed;
(5) by 14 parts of peanut oil, 11 parts of duck wheat brass, long-term effect capric acid glyceryl ester -6 parts of zinc oxide, be added to 5 times
In 0.1-0.5% mineral oil solutions, being stored at room temperature 12h is uniformly dissolved it, is well mixed in 50 DEG C of condition high-speed stirreds, rear to add
It is microwave treatment 15min under 2450MHz, power 800w to enter 0.5 part of calcium carbonate in microwave frequency, and material is produced after well mixed
Ⅱ;
(6) material I and material II are mixed, is warming up to 60 DEG C and is sufficiently stirred 15min, it is rear to stand room temperature 1000rpm/ again
40 DEG C of insulated and stirred 20min of min, it is rear to stand room temperature cooling, obtain mixing sticky material;Mixed material is added in mulser,
Acted on by mulser and produce valve derusting lubricant.
Embodiment 2
A kind of valve derusting lubricant, the raw material components for having following parts by weight are made:
34 parts of isopropyl acetate, 21 parts of laurene, 14 parts of propane diols, 14 parts of dimethicone, 29 parts of mineral oil, honey 27
Part, 11 parts of hyaluronic acid, 20 parts of down alkene, 12 parts of Tea Polyphenols, 800021 parts of modified poly ethylene glycol, 9 parts of lignosulfite,
6 parts of tertiary butyl hydroxyl fennel seeds brain, 23 parts of chaff amine, 13 parts of SAIB, polyurethane-acrylate composite emulsion
8 parts, 14 parts of duck wheat brass, 12 parts of peanut oil, long-term effect capric acid glyceryl ester -6 parts of zinc oxide, 0.5 part of calcium carbonate.
The preparation method of modified poly ethylene glycol 8000:Macrogol 8000 is added in reactor, starts stirring,
Quantitative ethanol solution is slowly added to, heated up 40 DEG C of addition hydrogen peroxide solutions, and 80 DEG C are warming up in 25min, is incubated 1h, decompression is de-
Water, quantitative boric acid is added, be warming up to 200 DEG C in 20min, stir 25min, when question response thing starts retrogradation, dehydration, 180 DEG C
Gelation time releases green-yellow thick liquid while hot when being 60-90s, obtain being denatured the precursor of modified poly ethylene glycol 8000 after cooling
Thing, add in backward precursor and 0.3 part of turpentine oil, 0.5 part of poly dimethyl allyl chlorination are added in 0.5 part of silica
Ammonium, be sufficiently mixed after microwave treatment 15min under microwave frequency 2450MHz, power 700W, add 1 part of rilanit special,
0.5 part of kayexalate and 0.5 part of N methyldiethanol amine, continue microwave treatment 5min, microwave treatment after being well mixed
Sealing and standing 3h in 0-5 DEG C of environment is transferred to after end immediately, 125-130 DEG C of insulation mixing 15min is then heated to, is mixed to gained
10 parts of 0-5 DEG C of cold water are added in compound, 1h is stood after being sufficiently mixed, is subsequently heated to reflux state and is incubated mixing 5min, and certainly
Room temperature so is cooled to, is finally sent into spray dryer, it is modified poly ethylene glycol 8000 to dry gained particle.
The polyurethane-acrylate composite emulsion preparation method:Polyurethane-acrylate is added in deionized water,
80 DEG C of heating treats that material is completely dissolved, and bisphenol A type epoxy resin and trimethylolpropane tris propionic ester are added in backward solution
1000rpm/min, 15min being stirred, be prepared into low crosslinking degree nucleocapsid, backward emulsion adds glutaraldehyde, 15min is stirred at room temperature, after
0 DEG C of placement 24H in refrigerator is placed it in, is irradiated after being drawn off, radiation parameter is:Under Co-60 radiation, 15KGy spokes
According to 4h, room temperature is placed after taking-up.
The long-term effect capric acid glyceryl ester-zinc oxide preparation method is:By potassium chlorate, capric acid glyceryl ester, zinc oxide
It is placed in reaction bulb, shake well, after making reactant well mixed, heating, obtained carbon dioxide is dissolved in containing carbon
In sour sodium, hydrogenperoxide steam generator, it is 9-10 to make into PH, and concentration is 4-5% stablizing solution;By stablizing solution and appropriate capric acid
Glyceryl ester, 1.5-3% agar, inorganic filler etc. are well mixed, obtain 1 solidification material components I;Again by hydrochloric acid, capric acid triglycerin
After ester, 1.5-3% agar and inorganic filler are fully adjusted, shape acid releasing agent compositionⅱ must be solidified;Components I and compositionⅱ are mixed afterwards
Close it is uniform, after be put into dryer and dry moisture and be put into 20-30%, then by material in comminutor, nano particle is made and produces
Long-term effect capric acid glyceryl ester-zinc oxide.
Preferably, its preparation method is as follows:
(1) 34 parts of isopropyl acetate, 21 parts of laurene, 14 parts of propane diols are first added into 60 DEG C of heating of heating in deionized water
It is sufficiently uniformly dissolved, 14 parts of dimethicone, 29 parts of mineral oil, 27 parts of honey, 11 parts of hyaluronic acid is added in backward solution, first
90 DEG C are heated to, thing to be mixed dissolves and is cooled to room temperature grinds stirring in the heating grinder that rotating speed is 1500rpm/min
Uniformly, the mixture I that 3h is dried in 50 DEG C of baking ovens is taken out afterwards;
(2) by step 1 gained mixture I and 20 parts of down alkene, 12 parts of Tea Polyphenols, 800021 parts of modified poly ethylene glycol, Asia
9 parts of sulphate pulp waste liquid, 6 parts of tertiary butyl hydroxyl fennel seeds brain are added in heated at high speed mixing mill, 2000rpm/min stirrings
It is well mixed;
(3) material, which is added in fluid-flywheel clutch, after being well mixed in step 2 is mixed, rear to add in refiner,
Refine repeatedly refines material, so as to obtain valve derusting lubricant matrix;
(4) by the valve obtained in step 3 derusting lubricant matrix and 23 parts of chaff amine, SAIB 13
Part, 8 parts of polyurethane-acrylate composite emulsion are heated at high temperature homogenizers at 60 DEG C and are well mixed, and are in microwave frequency
Microwave treatment 15min under 2450MHz, power 800w, material I is produced after well mixed;
(5) by 12 parts of peanut oil, 14 parts of duck wheat brass, long-term effect capric acid glyceryl ester -6 parts of zinc oxide, be added to 5 times
In 0.1-0.5% mineral oil solutions, being stored at room temperature 4h is uniformly dissolved it, is well mixed in 30 DEG C of condition high-speed stirreds, rear to add
It is microwave treatment 10-30min under 2450MHz, power 800w to enter 0.5 part of calcium carbonate in microwave frequency, and thing is produced after well mixed
Material II;
(6) material I and material II are mixed, is warming up to 60 DEG C and is sufficiently stirred 15min, it is rear to stand room temperature 2000rpm/ again
20 DEG C of insulated and stirred 20min of min, it is rear to stand room temperature cooling, obtain mixing sticky material;Mixed material is added in mulser,
Acted on by mulser and produce valve derusting lubricant.
To carrying out experiment investigation respectively in embodiment provided by the invention, embodiment 1 and 2 made valve of embodiment are derusted
Lubricant is investigated, and is investigated as shown in table 1,2.
The lubricating oil of table 1 investigates standard
The valve of table 2 derusting lubricant investigates result
From above detection method and testing result:Valve derusting lubricant is prepared to meet the requirements of the standard, and material
It is safe and non-toxic, environmentally safe, do not damage the objects such as valve, and improve profit containing surface epoxidation group in grease material
Lubricating oil abrasion resistance, being derusted using late gate, lubricating oil is recyclable to re-work utilization, realizes that huge profit saves resource, and this product product
It is of fine quality it is good, using lasting, part can be got rusty using prevention valve in advance, and lubricate valve working;When part gets rusty, it can be used clear
Except rusty stain dirt maintains valve;Prepare valve derusting lubricant it is nontoxic to human body, user can be safe to use.
The general principle and principal character and advantages of the present invention of the present invention has been shown and described above.The technology of the industry
Personnel are it should be appreciated that the present invention is not limited to the above embodiments, and the simply explanation described in above-described embodiment and specification is originally
The principle of invention, without departing from the spirit and scope of the present invention, various changes and modifications of the present invention are possible, these changes
Change and improvement all fall within the protetion scope of the claimed invention.The claimed scope of the invention by appended claims and its
Equivalent thereof.
Claims (5)
- The lubricant 1. a kind of valve derusts, it is characterised in that the raw material for having following parts by weight is made:Isopropyl acetate 5-60 parts, laurene 4-50 parts, propane diols 2-34 parts, dimethicone 3-19 parts, mineral oil 2-59 parts, Honey 2-37 parts, hyaluronic acid 3-18 parts, down alkene 3-30 parts, Tea Polyphenols 2-18 parts, modified poly ethylene glycol 80002-23 parts, Asia Sulphate pulp waste liquid 2-17 parts, tertiary butyl hydroxyl fennel seeds brain 2-10 parts, chaff amine 3-60 parts, SAIB 2-23 Part, polyurethane-acrylate composite emulsion 1-8 parts, duck wheat brass 2-16 parts, peanut oil 3-34 parts, long-term effect capric acid three are sweet Grease-zinc oxide 3-16 parts, calcium carbonate 0.5-2 parts.
- The lubricant 2. valve according to claim 1 derusts, it is characterised in that:It is prepared by the modified poly ethylene glycol 8000 Method:Macrogol 8000 is added in reactor, starts stirring, quantitative ethanol solution is slowly added to, heats up 60-160 DEG C Hydrogen peroxide solution is added, 40-80 DEG C is warming up in 20-60min, 1-5h is incubated, decompression dehydration, adds quantitative boric acid, 20-50min is warming up to 200 DEG C, stirs 20-40min, and when question response thing starts retrogradation, dehydration, 180 DEG C of gelation times are 60- Green-yellow thick liquid is released during 90s while hot, obtains being denatured the precursor of modified poly ethylene glycol 8000 after cooling, in backward precursor Add and 0.3-1.5 parts turpentine oil, 0.5-1 part PDDAs are added in 0.5-2 part silica, it is fully mixed Close after microwave treatment 5-30min under microwave frequency 2450MHz, power 700W, add 1-2 parts rilanit special, 0.5-1 parts Kayexalate and 0.5-1 part N methyldiethanol amines, continue microwave treatment 5min after being well mixed, microwave treatment terminates It is transferred to sealing and standing 3h in 0-5 DEG C of environment immediately afterwards, is then heated to 125-130 DEG C of insulation mixing 10-30min, is mixed to gained 6-18 0-5 DEG C of cold water of part is added in compound, 1h is stood after being sufficiently mixed, is subsequently heated to reflux state and is incubated mixing 5-30min, And room temperature is naturally cooled to, finally it is sent into spray dryer, it is modified poly ethylene glycol 8000 to dry gained particle.
- The lubricant 3. valve according to claim 2 derusts, it is characterised in that:The polyurethane-acrylate Composite Milk Liquid and preparation method thereof:Polyurethane-acrylate is added in deionized water, 60-120 DEG C of heating treats that material is completely dissolved, backward molten Bisphenol A type epoxy resin and trimethylolpropane tris propionic ester 1000-3000rpm/min are added in liquid, stirs 15-30min, system It is standby to add glutaraldehyde into low crosslinking degree nucleocapsid, backward emulsion, 10-40min is stirred at room temperature, after place it in refrigerator 0 ± 5 DEG C 12-24H is placed, is irradiated after being drawn off, radiation parameter is:Under Co-60 radiation, 10-20KGy irradiation 1-4h, after taking-up Room temperature is placed.
- The lubricant 4. valve according to claim 3 derusts, it is characterised in that:The long-term effect capric acid glyceryl ester-oxygen Changing zinc preparation method is:Potassium chlorate, capric acid glyceryl ester, zinc oxide are placed in reaction bulb, shake well, mix reactant After uniformly, heating, it is 9-10 that obtained carbon dioxide, which is dissolved in containing PH in sodium carbonate, hydrogenperoxide steam generator, is made into, dense Spend the stablizing solution for 4-5%;Stablizing solution and appropriate capric acid glyceryl ester, 1.5-3% agar, inorganic filler etc. are mixed Uniformly, 1 solidification material components I is obtained;After hydrochloric acid, capric acid glyceryl ester, 1.5-3% agar and inorganic filler are fully adjusted again, Shape acid releasing agent compositionⅱ must be solidified;Components I and compositionⅱ are well mixed afterwards, after be put into dryer dry moisture in 20- 30%, then material is put into comminutor, nano particle is made and produces long-term effect capric acid glyceryl ester-zinc oxide.
- The lubricant 5. valve according to claim 4 derusts, it is characterised in that:Preferably, its preparation method is as follows:(1) first isopropyl acetate 5-60 parts, laurene 4-50 parts, propane diols 2-34 parts are added in deionized water and heats 40-80 DEG C heating is sufficiently uniformly dissolved, and dimethicone 3-19 parts, mineral oil 2-59 parts, honey 2-37 parts, thoroughly are added in backward solution Bright matter acid 3-18 parts, 80-180 DEG C is first heated to, it is 1000-5000rpm/ that thing to be mixed, which dissolves and is cooled to room temperature in rotating speed, Grind and stir in min heating grinder, take out the mixture I that 1-12h is dried in 50-120 DEG C of baking oven afterwards;(2) by step 1 gained mixture I and down alkene 3-30 parts, Tea Polyphenols 2-18 parts, the 2-23 parts of modified poly ethylene glycol 8000, Lignosulfite 2-17 parts, tertiary butyl hydroxyl fennel seeds brain 2-10 parts are added in heated at high speed mixing mill, 1000- 3000rpm/min is uniformly mixed;(3) material, which is added in fluid-flywheel clutch, after being well mixed in step 2 is mixed, rear to add in refiner, is carried out Refining repeatedly refines material, so as to obtain valve derusting lubricant matrix;(4) by the valve obtained in step 3 derusting lubricant matrix and chaff amine 3-60 parts, SAIB 2-23 Part, polyurethane-acrylate composite emulsion 1-8 parts are heated at high temperature homogenizer at 30-90 DEG C and are well mixed, and are in microwave frequency Microwave treatment 10-30min under 2450MHz, power 800w, material I is produced after well mixed;(5) by peanut oil 3-34 parts, duck wheat brass 2-16 parts, long-term effect capric acid glyceryl ester-zinc oxide 3-16 parts, be added to In 5 times of 0.1-0.5% mineral oil solutions, being stored at room temperature 1-24h is uniformly dissolved it, is mixed in 30-50 DEG C of condition high-speed stirred Uniformly, it is microwave treatment 10-30min under 2450MHz, power 800w to add calcium carbonate 0.5-2 parts afterwards in microwave frequency, and mixing is equal Material II is produced after even;(6) material I and material II are mixed, is warming up to 40-60 DEG C and is sufficiently stirred 15-60min, it is rear to stand room temperature 1000- again 5000rpm/min 20-40 DEG C insulated and stirred 20-40min, it is rear to stand room temperature cooling, obtain mixing sticky material;By mixture Material is added in mulser, is acted on by mulser and is produced valve derusting lubricant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710688403.3A CN107573989A (en) | 2017-08-12 | 2017-08-12 | A kind of valve derusting lubricant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710688403.3A CN107573989A (en) | 2017-08-12 | 2017-08-12 | A kind of valve derusting lubricant |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107573989A true CN107573989A (en) | 2018-01-12 |
Family
ID=61034906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710688403.3A Pending CN107573989A (en) | 2017-08-12 | 2017-08-12 | A kind of valve derusting lubricant |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107573989A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108753131A (en) * | 2018-04-30 | 2018-11-06 | 安徽恒益纺织科技有限公司 | A kind of water-repellent paint for textile fabric |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101165075A (en) * | 2007-09-07 | 2008-04-23 | 香港生产力促进局 | Polyurethane-acrylic ester composite emulsion and preparation method thereof |
CN103695917A (en) * | 2013-11-29 | 2014-04-02 | 明光市留香泵业有限公司 | Water-emulsion-type antirust liquid and preparation method thereof |
CN105296104A (en) * | 2015-10-21 | 2016-02-03 | 和县科嘉阀门铸造有限公司 | Rust-preventative oil for valve factory packaging |
-
2017
- 2017-08-12 CN CN201710688403.3A patent/CN107573989A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101165075A (en) * | 2007-09-07 | 2008-04-23 | 香港生产力促进局 | Polyurethane-acrylic ester composite emulsion and preparation method thereof |
CN103695917A (en) * | 2013-11-29 | 2014-04-02 | 明光市留香泵业有限公司 | Water-emulsion-type antirust liquid and preparation method thereof |
CN105296104A (en) * | 2015-10-21 | 2016-02-03 | 和县科嘉阀门铸造有限公司 | Rust-preventative oil for valve factory packaging |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108753131A (en) * | 2018-04-30 | 2018-11-06 | 安徽恒益纺织科技有限公司 | A kind of water-repellent paint for textile fabric |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE69233289T2 (en) | Recovery of carbon dioxide from combustion exhaust gas | |
CN106519637A (en) | Waterborne polyurethane slurry for producing synthetic leather bass through wet method | |
CN107573989A (en) | A kind of valve derusting lubricant | |
CN103305325B (en) | Release agent and preparation method thereof | |
CN107648177A (en) | A kind of profit repairs facial mask for releiving for sensitive skin | |
CN105780232A (en) | Antibacterial blended recuperated cotton yarn and preparation method thereof | |
CN106884330A (en) | A kind of emulsion type carbon fiber sizing agent and its preparation method and application | |
CN106896459A (en) | Selfreparing optical cable enhancing core containing microcapsules and preparation method thereof | |
CN108329738A (en) | Peach colloidal solution and preparation method thereof | |
CN105250200A (en) | Preparation method of microcapsule type eye shadow | |
CN106085213A (en) | A kind of processing technology of steel surface renovation agent | |
CN109793677A (en) | A kind of creams and preparation method thereof | |
CN115671265A (en) | Method for preparing contour injection composition | |
CN211965372U (en) | Adopt biological method to restore device of compound heavy metal contaminated soil | |
CN105733775A (en) | Transmission shaft lubricating oil prepared from residual oil | |
CN104368032B (en) | A kind of wound repair biogel material and preparation method thereof | |
CN107157851A (en) | A kind of preparation method of chamomile tearing facial mask | |
CN105483660A (en) | Preparing method for shell stamped parts | |
CN109965105A (en) | A kind of production technology of feed grade liquid natural lutein product | |
CN108034297A (en) | A kind of preparation method of mineral coating graphene additive | |
CN106633946B (en) | A kind of rubber powder modified emulsified asphalt and preparation method thereof | |
CN209582432U (en) | Low temp freezing appts are used in a kind of processing of cosmetics | |
CN112972352B (en) | Preparation method of color-changeable essential oil hair care module | |
CN109513688A (en) | A kind of method for cleaning of aluminum alloy doorframe | |
CN107854363A (en) | A kind of skin protection bath cream containing mulberry leaf |
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 | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20180112 |
|
RJ01 | Rejection of invention patent application after publication |