Calcium carbonate γ-aminopropyl triethoxysilane properties-correcting agent
Technical field
The invention belongs to a kind of production method of calcium carbonate powder.
Background technology
At present, calcium carbonate is widely used in papermaking, plastics, plastics film, chemical fibre, rubber, tackiness agent, sealing agent, daily-use chemical industry, makeup, building materials, coating, paint, ink, putty, sealing wax, putty, carpet veneer is packed, medicine, food is (as chewing gum, chocolate), in feed, its effect has: increase small product size, reduce costs, improve processing characteristics (as adjusting viscosity, rheological property, curability), improve dimensional stability, reinforcement or half reinforcement, improve printing performance, improve physicals (as thermotolerance, extinction, wear resistance, flame retardant resistance, whiteness, glossiness) etc.Light calcium carbonate; Also known as precipitated chalk, be called for short fine particle calcium carbonate, that the raw material calcinings such as Wingdale are generated lime (main component is calcium oxide) and carbonic acid gas, the digestion lime that adds water again generates milk of lime (main component is calcium hydroxide), and then pass into carbonic acid gas carbonization milk of lime generation precipitation of calcium carbonate, finally by dehydration, dry and pulverize and obtain.Or first carry out replacement(metathesis)reaction with sodium carbonate and calcium chloride and generate precipitation of calcium carbonate, then obtain through dehydration, drying and pulverizing.Because the settling volume (2.4-2.8mL/g) of light calcium carbonate is larger than the settling volume (1.1-1.9mL/g) of water-ground limestone, so be referred to as light calcium carbonate.The technological process of production of water-ground limestone has two kinds.Dry technology for production flow process: the first calcite, Wingdale, chalk, shell etc. that ship from stone quarry of picking, to remove gangue; Then with crusher, coarse breaking is carried out to Wingdale, cover that (pendulum-type) abrasive dust is broken obtains microlith limestone flour again with thunder, finally carry out classification with grading machine to abrasive dust, the powder meeting granularity requirements is put in storage as the packing of product, otherwise returns pulverizing mill abrasive dust again.Wet process technique flow process: first dry method fine powder is made suspension and be placed in grinding machine and pulverize further, just obtained superfine heavy calcium carbonate after dehydration, drying.The industrial production process of modified active calcium carbonate, by the calcium carbonate powder particle of Monodispersed, carry out the process of liquid phase Surface coating, the nm-class active calcium carbonate particle obtained is between 25 ~ 100nm, specific surface is greater than 25m2/g, size distribution GSD is 1.57, and oil-absorption(number) is less than 28g/100gCaCO3, and soilless sticking phenomenon.The excellent product performance obtained, can be used as the functional stuffing in high-grade rubber, plastics and vehicle paint base.
Retrieve through Chinese publication, find calcium carbonate application for a patent for invention 53; Do not find the scheme identical with present patent application.
Summary of the invention
The object of the invention is to; A kind of calcium carbonate γ-aminopropyl triethoxysilane properties-correcting agent is proposed.
Calcium carbonate γ-aminopropyl triethoxysilane properties-correcting agent of the present invention, it is characterized in that: by weight, by propylene maleic acid rosin calcium 1-3 part, γ-aminopropyl triethoxysilane 25-30 part, sodium carbonate 5-8 part, vinyl pyridine co-polymer 3-5 part, ethylene glycol 5-8 part, Vanay 5-6 part, dioctyl tin 1--2 part, water 50-60 part forms.
Calcium carbonate γ-aminopropyl triethoxysilane preparation method for modifier of the present invention, it is characterized in that: by weight, fill a prescription by propylene maleic acid rosin calcium 1-3 part, γ-aminopropyl triethoxysilane 25-30 part, sodium carbonate 5-8 part, vinyl pyridine co-polymer 3-5 part, ethylene glycol 5-8 part, Vanay 5-6 part, dioctyl tin 1--2 part, water 50-60 part forms, and stirs 20-30 minute, obtain product at 85 ~ 95 DEG C.
γ-aminopropyl triethoxysilane; Chemical structural formula: NH
2cH
2cH
2cH
2si (OC
2h
5)
3
The present invention compared with prior art its beneficial effect is: have design science reasonable, and technique is simple, safe reliability, is easy to control, easy to operate, is applicable to scale operation, the advantages such as production cost is low.
Embodiment
Below in conjunction with embodiment, the invention will be further described, but embodiments of the present invention are not limited thereto.
All raw materials of the present invention can buy acquisition.
Embodiment 1
Calcium carbonate γ-aminopropyl triethoxysilane properties-correcting agent of the present invention, it is characterized in that: by weight, by propylene maleic acid rosin calcium 1-3 part, γ-aminopropyl triethoxysilane 25-30 part, sodium carbonate 5-8 part, vinyl pyridine co-polymer 3-5 part, ethylene glycol 5-8 part, Vanay 5-6 part, dioctyl tin 1--2 part, water 50-60 part forms.
Embodiment 2
Calcium carbonate γ-aminopropyl triethoxysilane preparation method for modifier of the present invention, it is characterized in that: by weight, fill a prescription by propylene maleic acid rosin calcium 1-3 part, γ-aminopropyl triethoxysilane 25-30 part, sodium carbonate 5-8 part, vinyl pyridine co-polymer 3-5 part, ethylene glycol 5-8 part, Vanay 5-6 part, dioctyl tin 1--2 part, water 50-60 part forms, and stirs 20-30 minute, obtain product at 85 ~ 95 DEG C.
Embodiment 3
Calcium carbonate γ-aminopropyl triethoxysilane preparation method for modifier of the present invention, it is characterized in that: by weight, fill a prescription by propylene maleic acid rosin calcium 3 parts, γ-aminopropyl triethoxysilane 25 parts, 5 parts, sodium carbonate, vinyl pyridine co-polymer 3 parts, ethylene glycol 5 parts, Vanay 5 parts, dioctyl tin 1 part, 50 parts, water composition, stirs 20-30 minute, obtains product at 85 ~ 95 DEG C.
Embodiment 4
Calcium carbonate γ-aminopropyl triethoxysilane preparation method for modifier of the present invention, it is characterized in that: by weight, fill a prescription by propylene maleic acid rosin calcium 3 parts, γ-aminopropyl triethoxysilane 30 parts, 8 parts, sodium carbonate, vinyl pyridine co-polymer 5 parts, ethylene glycol 8 parts, Vanay 6 parts, dioctyl tin 2 parts, 60 parts, water composition, stirs 20-30 minute, obtains product at 85 ~ 95 DEG C.
Embodiment 5
Calcium carbonate γ-aminopropyl triethoxysilane preparation method for modifier of the present invention, it is characterized in that: by weight, fill a prescription by propylene maleic acid rosin calcium 3 parts, γ-aminopropyl triethoxysilane 25 parts, 5 parts, sodium carbonate, vinyl pyridine co-polymer 3 parts, ethylene glycol 8 parts, Vanay 5 parts, dioctyl tin 2 parts, 50 parts, water composition, stirs 20-30 minute, obtains product at 85 ~ 95 DEG C.
Embodiment 6
Calcium carbonate γ-aminopropyl triethoxysilane preparation method for modifier of the present invention, it is characterized in that: by weight, fill a prescription by propylene maleic acid rosin calcium 3 parts, γ-aminopropyl triethoxysilane 30 parts, 5 parts, sodium carbonate, vinyl pyridine co-polymer 5 parts, ethylene glycol 5 parts, Vanay 6 parts, dioctyl tin 1 part, 60 parts, water composition, stirs 20-30 minute, obtains product at 85 ~ 95 DEG C.
Product of the present invention, uses through production firm, and produce modified active superfine heavy calcium carbonate product, reaction effect is fine.
Propylene maleic acid rosin calcium can be prepared as follows: material ratio is, rosin: vinylformic acid: MALEIC ANHYDRIDE: the mol ratio of calcium oxide is 1:0.3:0.1:0.3; By rosin heating and melting under an inert gas, heat up 180-200 DEG C, add MALEIC ANHYDRIDE 5-15 parts, 180-200 DEG C, carry out addition reaction 1.5-2 hours; Control to drip vinylformic acid with the speed to add for 45-50 minutes, then, enter calcium oxide, be warming up to 250-260 DEG C of reactions 80-90 minutes, sampling is dripped on sheet glass and is cooled, and is transparently terminal.Cooling lets cool and obtains product, for subsequent use.