Summary of the invention
The present invention provides a kind of hot core sand inorganic binder and preparation method thereof, it has adhesion strength high, and viscosity is low, uses
In thermal method coremaking, the advantages that sand fluidity is good, and sand core moisture resistance is good, sand mold intensity stabilization.
The present invention adopts the following technical scheme:
A kind of hot core sand inorganic binder, the hot core sand inorganic binder includes following component and its weight percent:
Phosphoric acid 50~53%, aluminium hydroxide 11~12%, boric acid 1.87~2.50%, silicic acid 0.89~0.92%, magnesia 1.14~
1.57%, copper oxide 0.05~0.07%, water 32~34%.
Preferably, the phosphoric acid is 85% industrial phosphoric acid.
Preferably, the silicic acid is 1000 mesh solid powderies.
Preferably, the magnesia is chemical pure, 600 mesh powder shape substance of granularity.
Preferably, the boric acid is technical grade.
Preferably, the copper oxide is chemical pure, 600 mesh powder shape substance of granularity.
The preparation method of above-mentioned hot core sand inorganic binder, includes the following steps:
(1) phosphoric acid and aluminium-hydroxide powder and water are added in three mouthfuls of reaction kettles, turn on agitator and heater, slowly
It is heated to 180~200 DEG C;
(2) to which after reaction, boric acid is added in reaction kettle in reaction kettle, continue heating, stirring, until in reaction kettle
Solution is transparent;
(3) silicic acid is added, continues heating, stir about 15min, mixing speed can be improved at this time, to improve silicic acid
Dispersion degree, accelerate silicic acid powder dissolution, until reaction kettle in solution it is transparent;
(4) magnesia is added, continues heating, stirring, until solution is transparent in reaction kettle;
(5) copper oxide is added, continues heating, stirring, until solution is transparent in reaction kettle;
(6) it discharges, it is cooling to solution, obtain hot core sand inorganic binder.
The application method of above-mentioned hot core sand inorganic binder mixes sand with the hot core sand inorganic binder in sand mixer
After system, blasting unit is added, penetrates sand mold processed in core shooter, 150~200 DEG C of mould heating-up temperature, sand sample curing molding ejects to obtain the final product
Sand mold or sand core.
The hot core sand inorganic binder of the present invention is applied to hot box shoot core machine and prepares sand mold or sand core, with compared with firmly, mixes
Good sand room temperature is non-sclerous, and only heating could harden, therefore when this binder prepares sand mold or sand core does not need curing agent;With
Thermmohardening is compared with hot-air solidification, requires heat hardening, but molding and core making technique is different, mixed sand is made in compressed air
It injects type chamber in a few seconds under and is compacted, therefore it is required that binder viscosity is low, mixed sand good fluidity.
This binder uses polynary micro composite modified approach, joined micro oxygen while silicic acid is added in component
Change copper, silicic acid reduces the degree of neutralization of binder, keeps binder solution transparent, but sample shelf stability declines, copper oxide
It is added, due to forming complex compound mantoquita, improves sample shelf stability, sample is stored 8 hours under 40% humidity, and tension is strong
Within 10%, some even improves 11% for degree decline.
Hot core sand inorganic binder obtained by technical solution of the present invention is non-toxic and tasteless pollution-free, and viscosity is low, has after mixing with sand
There is preferable mobility, meets the production requirement of hot box shoot core machine, the sand mold or sand core stability obtained after being heating and curing is good,
Tensile strength is high, and product has broad application prospects, and economic benefit and social benefit are significant.
Specific embodiment
To keep the present invention easier to understand, specific embodiments of the present invention are further illustrated below.
The hot core sand inorganic binder synthesis of the phosphate of the present application and sand mold preparating example are as follows:
Example one:
53 kilograms of 85% industrial phosphoric acid, 11 kilograms of aluminium-hydroxide powder, 1.92 kilograms of boric acid, silicic acid 0.89 are weighed in proportion
Kilogram, 1.14 kilograms of magnesia, 0.05 kilogram of copper oxide, 32 kilograms of water.
Preparation step:
1,53 kilograms of industrial phosphoric acids and 11 kilograms of aluminium-hydroxide powders and 32 kg of water are added in three mouthfuls of reaction kettles, are opened
Blender and heater are opened, is slowly heated to 180~200 DEG C;
2, to which after reaction, 1.92 kilograms of boric acid are added in reaction kettle in reaction kettle, continue heating, stirring, until
Solution is transparent in reaction kettle;
3,0.89 kilogram of silicic acid is added, continues heating, stirring, until solution is transparent in reaction kettle;
4, be added 1.14 kilograms of magnesia, continue heating, stirring it is transparent to solution;
5, be added 0.05 kilogram of copper oxide, continue heating, stirring it is transparent to solution;
Discharging, to solution cooling, viscosimetric and for making sand sample.
Mulling and sand mold preparation: preparing 40~70 mesh quartz sands, prepares binder by sand 2.5%, mulling first is added in sand
Machine starts sand mixer, then slowly pours into binder, continue mulling 2 minutes after adding, then shake out.Blasting unit is added in sand,
By compressed air by 160 DEG C of sand injection of mold, it according to sand core thickness, can be opened within about 4~5 minutes, eject sand core.
Part sand is taken to penetrate system " 8 " word sand sample and bending strength sample on testing machine simultaneously, for examining sand mold mobility and sand mold strong
Degree.It penetrates that specimen surface processed is bright and clean, and corner angle are clear, shows that good fluidity, probe intensity are shown in Table 1.
Table 1
Example two:
52 kilograms of 85% industrial phosphoric acid, 11 kilograms of aluminium-hydroxide powder, 2.44 kilograms of boric acid, silicic acid 0.92 are weighed in proportion
Kilogram, 1.57 kilograms of magnesia, 0.07 kilogram of copper oxide, 32 kilograms of water.
Preparation step:
1,52 kilograms of industrial phosphoric acids and 11 kilograms of aluminium-hydroxide powders and 32 kg of water are added in three mouthfuls of reaction kettles, are opened
Blender and heater are opened, is slowly heated to 180~200 DEG C;
2, to which after reaction, 2.44 kilograms of boric acid are added in reaction kettle in reaction kettle, continue heating, stirring, until
Solution is transparent in reaction kettle;
3,0.92 kilogram of silicic acid is added, continues heating, stirring, until solution is transparent in reaction kettle;
4, be added 1.57 kilograms of magnesia, continue heating, stirring it is transparent to solution;
5, be added 0.07 kilogram of copper oxide, continue heating, stirring it is transparent to solution;
Discharging, to solution cooling, viscosimetric and for making sand sample.
Mulling and sand mold preparation: preparing 40~70 mesh quartz sands, prepares binder by sand 3%, sand mixer first is added in sand,
Start sand mixer, then slowly pours into binder, continue mulling 2 minutes after adding, then shake out.Blasting unit is added in sand, is led to
Overcompression air is injected sand in 180 DEG C of mold, according to sand core thickness, can be opened within about 4~5 minutes, ejects sand core.Together
When take part sand to penetrate system " 8 " word sand sample and bending strength sample on testing machine, for examining sand mold mobility and sand mold intensity.
It penetrates that specimen surface processed is bright and clean, and corner angle are clear, shows that good fluidity, probe intensity are shown in Table 2.
Table 2
Example three:
52 kilograms of 85% industrial phosphoric acid, 12 kilograms of aluminium-hydroxide powder, 1.87 kilograms of boric acid, silicic acid 0.90 are weighed in proportion
Kilogram, 1.16 kilograms of magnesia, 0.07 kilogram of copper oxide, 32 kilograms of water.
Preparation step:
1,52 kilograms of industrial phosphoric acids and 12 kilograms of aluminium-hydroxide powders and 32 kg of water are added in three mouthfuls of reaction kettles, are opened
Blender and heater are opened, is slowly heated to 180~200 DEG C;
2, to which after reaction, 1.87 kilograms of boric acid are added in reaction kettle in reaction kettle, continue heating, stirring, until
Solution is transparent in reaction kettle;
3,0.90 kilogram of silicic acid is added, continues heating, stirring, until solution is transparent in reaction kettle;
4, be added 1.16 kilograms of magnesia, continue heating, stirring it is transparent to solution;
5, be added 0.07 kilogram of copper oxide, continue heating, stirring it is transparent to solution;
Discharging, to solution cooling, viscosimetric and for making sand sample.
Mulling and sand mold preparation: preparing 40~70 mesh quartz sands, prepares binder by sand 2.5%, mulling first is added in sand
Machine starts sand mixer, then slowly pours into binder, continue mulling 2 minutes after adding, then shake out.Blasting unit is added in sand,
By compressed air by 175 DEG C of sand injection of mold, it according to sand core thickness, can be opened within about 4~5 minutes, eject sand core.
Part sand is taken to penetrate system " 8 " word sand sample and bending strength sample on testing machine simultaneously, for examining sand mold mobility and sand mold strong
Degree.It penetrates that specimen surface processed is bright and clean, and corner angle are clear, shows that good fluidity, probe intensity are shown in Table 3.
Table 3
Example four:
50 kilograms of 85% industrial phosphoric acid, 11 kilograms of aluminium-hydroxide powder, 2.50 kilograms of boric acid, silicic acid 0.91 are weighed in proportion
Kilogram, 1.52 kilograms of magnesia, 0.07 kilogram of copper oxide, 34 kilograms of water.
Preparation step:
1,50 kilograms of industrial phosphoric acids and 11 kilograms of aluminium-hydroxide powders and 34 kg of water are added in three mouthfuls of reaction kettles, are opened
Blender and heater are opened, is slowly heated to 180~200 DEG C;
2, to which after reaction, 2.50 kilograms of boric acid are added in reaction kettle in reaction kettle, continue heating, stirring, until
Solution is transparent in reaction kettle;
3,0.91 kilogram of silicic acid is added, continues heating, stirring, until solution is transparent in reaction kettle;
4, be added 1.52 kilograms of magnesia, continue heating, stirring it is transparent to solution;
5, be added 0.07 kilogram of copper oxide, continue heating, stirring it is transparent to solution;
Discharging, to solution cooling, viscosimetric and for making sand sample.
Mulling and sand mold preparation: preparing 70~140 mesh quartz sands, prepares binder by sand 3.5%, mulling first is added in sand
Machine starts sand mixer, then slowly pours into binder, continue mulling 2 minutes after adding, then shake out.Blasting unit is added in sand,
By compressed air by 170 DEG C of sand injection of mold, it according to sand core thickness, can be opened within about 4~5 minutes, eject sand core.
Part sand is taken to penetrate system " 8 " word sand sample and bending strength sample on testing machine simultaneously, for examining sand mold mobility and sand mold strong
Degree.It penetrates that specimen surface processed is bright and clean, and corner angle are clear, shows that good fluidity, probe intensity are shown in Table 4.
Table 4
Finally, it should be noted that the above embodiments are merely illustrative of the technical solutions of the present invention rather than protects to the present invention
The limitation of range is protected, although the invention is described in detail with reference to the preferred embodiments, those skilled in the art should
Understand, it can be with modification or equivalent replacement of the technical solution of the present invention are made, without departing from the essence of technical solution of the present invention
And range.