Polyimide for special engineering plastics

Polyimide is the molecular structure contains an aromatic heterocyclic polymer compounds of polyimide-based chain links, the English name Polyimide (PI for short), can be divided into benzene-type PI, soluble PI, polyamide-imide (PAI) and polyetherimide (PEI) four categories.
PI is currently one of the best varieties of engineering plastics heat resistance, some varieties can withstand long-term 290 ? high temperature for a short period of time to withstand a high temperature of 490 ?, but also very low temperature, such as in the -269 ? liquid helium will not be brittle. In addition, mechanical properties, fatigue resistance, flame retardant, dimensional stability, electrical properties are good, molding shrinkage is small, resistant to oil, general acids and organic solvents, not alkali resistance, excellent friction resistance, abrasion properties. And PI is non-toxic, can be used to manufacture tableware and medical equipment, and withstand thousands of times disinfection.
PI moulding methods include compression moulding, impregnation, injection moulding, extrusion, die-casting, coating, casting, laminating, foaming and transfer moulding. PI has applications in aerospace, automotive, electronic and electrical appliances, industrial machinery, etc. It can be used as engine combustion system parts, jet engine components, compressor and generator parts, fasteners, spline joints and electronic contacts, as well as automotive engine parts, bearings, piston bushings, timing gears, printed wiring boards, insulating materials, heat-resistant cables, terminal blocks, sockets in the electronics industry, high temperature resistant self-lubricating bearings, and sockets in the machinery industry. High-temperature self-lubricating bearings, compressor blades and piston machine, sealing rings, equipment heat shield, thrust washers, bushings, etc..
Polyetherimide has excellent mechanical properties, electrical insulation properties, irradiation resistance, high and low temperature resistance and abrasion resistance, self-extinguishing, good melt flow, the shrinkage rate of the moulding is only 0.5 % ~ 0.7 %. PEI can be injection and extrusion moulding, post-processing is easier, can be adhesive or a variety of welding method and other materials, PEI in the electronics and electrical appliances, aerospace, automotive, medical equipment and other industries have been widely used. GE is the world’s largest producer of PEI, there are some engineering plastics modification company to provide PEI alloys and other modified products. The trend of development is the introduction of p-phenylenediamine structure or with other special engineering plastics alloy to improve its heat resistance; or with PC, PA and other engineering plastics alloy to improve its mechanical strength.
Polyamide-imide strength is currently the highest in the non-reinforced plastics, the colour of the material tensile strength of 190MPa, bending strength of 250MPa. 1.8MPa load heat deflection temperature of 274 ?. PAI has good ablation resistance and high temperature, high frequency under the electromagnetic properties of metals and other materials have good adhesive properties. Mainly used for gears, rollers, bearings and copier separation claws, etc., but also for aircraft ablative materials, magnetic permeability and structural materials.PAI by Amoco company was the first to develop a successful and commercialised, in addition to Amoco, Japan’s Toray can also provide moulding plastics. Its development direction is to enhance the modification, and alloy with other plastics.

Extended Reading?

PC-37 – Amine Catalysts (newtopchem.com)

Dabco foaming catalyst/polyurethane foaming catalyst NE300 – Amine Catalysts (newtopchem.com)

DABCO EG/PC CAT TD 33EG/Niax A-533 – Amine Catalysts (newtopchem.com)

FASCAT4100 catalyst – Amine Catalysts (newtopchem.com)

T120 1185-81-5 di(dodecylthio) dibutyltin – Amine Catalysts (newtopchem.com)

DABCO 1027/foaming retarder – Amine Catalysts (newtopchem.com)

DBU – Amine Catalysts (newtopchem.com)

bismuth neodecanoate/CAS 251-964-6 – Amine Catalysts (newtopchem.com)

stannous neodecanoate catalysts – Amine Catalysts (newtopchem.com)

polyurethane tertiary amine catalyst/Dabco 2039 catalyst – Amine Catalysts (newtopchem.com)

Synthesis of polyaniline

There are many synthesis methods for polyaniline, but the commonly used synthesis methods are two categories: chemical synthesis and electrochemical synthesis.
(1) Chemical synthesis method Chemical synthesis method is to use oxidant as initiator to make aniline monomer oxidative polymerisation in acidic medium, the specific implementation methods are as follows.
Chemical oxidative polymerisation The chemical oxidative polymerisation of polyaniline is to make the aniline monomer oxidatively polymerised by oxidising agent under acidic condition. Protonic acid is an important factor affecting the oxidative polymerisation of aniline, which mainly plays two roles: to provide the pH value of the reaction medium and the form of dopant into the polyaniline skeleton to give it a certain conductivity. Polymerisation is carried out simultaneously with on-site doping, and polymerisation and doping are completed simultaneously. Commonly used oxidising agents are: hydrogen peroxide, dichromate, persulfate, etc. Its synthesis reaction is mainly affected by the type and concentration of protonated acid, the type and concentration of oxidant, the concentration of monomer and the reaction temperature, reaction time and other factors. The advantages of chemical oxidation polymerisation are that it can produce polyaniline in large quantities, with low investment in equipment, simple process, suitable for industrial production, and it is the most commonly used synthesis method at present.
Emulsion polymerisation Emulsion polymerisation is a method of adding an initiator into an acidic emulsion system containing aniline and its derivatives. Emulsion polymerisation has the following advantages: environmentally friendly and low-cost water is used as the heat carrier, and the product does not need to be precipitated and separated to remove the solvent; the synthesised polyaniline has a higher molecular weight and solubility; if large molecules of sulfonic acid are used as the surfactant, doping can be completed in a single step to increase the conductivity of the conductive polyaniline; polyaniline can be made into an emulsion that is directly usable, so that the subsequent processing does not need to use expensive or toxic organic solvents, simplifying the process and making it easier to produce polyaniline. Organic solvents, simplify the process, reduce costs, but also to overcome the shortcomings of the traditional method of synthesis of polyaniline insoluble and non-melting.
Microemulsion polymerisation Microemulsion polymerisation is developed on the basis of emulsion method. The polymerisation system consists of water, aniline, surfactant and co-surfactant. The microemulsion dispersed phase droplet size (10~100 nm) is smaller than that of normal emulsion (10~200 nm), which is very favourable for the synthesis of nanoscale polyaniline. The nano-polyaniline particles may not only solve the defects of difficult processing and moulding, but also combine the polymer electrical conductivity and the unique physicochemical properties of nano-particles, therefore, the microemulsion method has become a research hotspot in the field since the first report of synthesizing polyaniline particles with the smallest particle size of 5 nm using this method in 1997. Currently, conventional O/W microemulsions are used for the synthesis of polyaniline nanoparticles, and the commonly used surfactants are DBSA, sodium dodecyl sulfate, etc., with particle sizes of about 10-40 nm. reversed-phase microemulsions (W/O) are used for the preparation of polyaniline nanoparticles, which can obtain smaller particle sizes (<10 nm), and a more uniform distribution of the particle sizes. This is due to the fact that fewer aniline monomers are dissolved in the aqueous core of the reversed-phase microemulsion than in the oil core of the conventional microemulsion.
Dispersion polymerisation The aniline dispersion polymerisation system is generally composed of aniline monomer, water, dispersant, stabiliser and initiator. The medium before the reaction is a homogeneous system, but the generated polyaniline is insoluble in the medium, when it reaches the critical chain length from the medium precipitation, with the help of stabilizers suspended in the medium, the formation of a stable dispersion system similar to the polymer emulsion. This method is currently used in the synthesis of polyaniline research is far less mature than the above three implementation methods, less research.
Mature, less research.
(2) Electrochemical synthesis method The electrochemical polymerisation of polyaniline includes the following methods: constant potential method, constant current method, dynamic potential scanning method and pulse polarisation method. Generally An is polymerised in acidic solution at the anode. Electrochemical synthesis of polyaniline is the oxidative polymerisation of An at the anode in an electrolyte solution containing An, resulting in a polyaniline film adhering to the electrode surface or a polyaniline powder deposited on the electrode surface.Diaz et al. prepared polyaniline films by electrochemical methods.
At present, PANI electrochromic films are mainly prepared by electrochemical methods, but there are several drawbacks in the preparation of PANI electrochromic films by electrochemical methods, such as: the inability to prepare electrochromic films on a large scale; the poor mechanical properties of the PANI film; and the poor adhesion of the PANI film to the conductive glass substrate.

Extended Reading?

PC-37 – Amine Catalysts (newtopchem.com)

Dabco foaming catalyst/polyurethane foaming catalyst NE300 – Amine Catalysts (newtopchem.com)

DABCO EG/PC CAT TD 33EG/Niax A-533 – Amine Catalysts (newtopchem.com)

FASCAT4100 catalyst – Amine Catalysts (newtopchem.com)

T120 1185-81-5 di(dodecylthio) dibutyltin – Amine Catalysts (newtopchem.com)

DABCO 1027/foaming retarder – Amine Catalysts (newtopchem.com)

DBU – Amine Catalysts (newtopchem.com)

bismuth neodecanoate/CAS 251-964-6 – Amine Catalysts (newtopchem.com)

stannous neodecanoate catalysts – Amine Catalysts (newtopchem.com)

polyurethane tertiary amine catalyst/Dabco 2039 catalyst – Amine Catalysts (newtopchem.com)

Method for preparing calcium propionate from calcium carbonate

Method for preparing calcium propionate from calcium carbonate

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Calcium propionate is white crystalline particles or crystalline powder. It is odorless or slightly smells of propionic acid, hygroscopic, easily soluble in water, and insoluble in alcohol. Calcium propionate is a newer food antifungal agent. It is the calcium salt of the acidic antifungal agent propionic acid. Under acidic conditions, it produces free propionic acid, which is weaker than sorbic acid and stronger than acetic acid. It has antibacterial effects and is effective against Aspergillus niger and Aspergillus niger. Aerophilic Bacillus has inhibitory effect. Calcium propionate is produced by reacting propionic acid with calcium hydroxide or calcium carbonate. In industry, calcium hydroxide is generally used as raw material. Calcium hydroxide is adjusted into a suspension in a reaction pot, propionic acid is added to react, the end point pH is 7~8, and the finished product is obtained after filtration and drying.

The method of preparing calcium propionate from calcium carbonate is as follows:

First, the raw material calcium carbonate is made into a water suspension, and the water used must be refined and purified. Remove impurities such as heavy metal magnesium. Put the CaCO3 aqueous suspension quantitatively into the neutralization reaction kettle, keep the temperature inside the kettle at 60-80°C, and add propionic acid while stirring. The neutralization reaction lasts for 2-3 hours. At this time, a large amount of CO2 gas escapes. Discharge through the condenser vent pipe. By adjusting the external heating temperature, adding acid and stirring speed, the reaction can reach optimal conditions. The pH value at the end of the reaction should be controlled at 7 to 8. This reaction is a reversible reaction. The CO2 gas should be discharged in time to better control the end of the reaction. . The neutralized aqueous solution is vacuum filtered, and the filtrate obtained is concentrated in an evaporator, and then placed in a crystallization tank for slow cooling and crystallization at normal temperature and pressure. The mother liquor can be returned to the evaporator and used 2 to 3 times before discarding. The separated solid is dried into small particles, crushed, measured, and packaged to obtain the finished product of calcium propionate.
amine catalyst Dabco 8154 – BDMAEE

2-ethylhexanoic-acid-potassium-CAS-3164-85-0-Dabco-K-15.pdf (bdmaee.net)

Dabco BL-11 catalyst CAS3033-62-3 Evonik Germany – BDMAEE

Polycat 9 catalyst CAS33329-35-6 Evonik Germany.pdf – BDMAEE

Dabco NE300 catalyst CAS10861-07-1 Evonik Germany.pdf (bdmaee.net)

Dabco 1027 Catalyst CAS100515-55-5 Evonik Germany – BDMAEE

Fomrez UL-28 Catalyst Dimethyltin Dioctadecanoate Momentive – BDMAEE

Polycat 77 catalyst CAS3855-32-1 Evonik Germany.pdf (bdmaee.net)

Polycat 41 catalyst CAS10294-43-5 Evonik Germany – BDMAEE

Polycat DBU catalyst CAS6674-22-2 Evonik Germany – BDMAEE