CN108385187B - High-strength airplane safety belt and preparation method thereof - Google Patents

High-strength airplane safety belt and preparation method thereof Download PDF

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CN108385187B
CN108385187B CN201711342800.1A CN201711342800A CN108385187B CN 108385187 B CN108385187 B CN 108385187B CN 201711342800 A CN201711342800 A CN 201711342800A CN 108385187 B CN108385187 B CN 108385187B
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safety belt
modified polyester
oil agent
reaction
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CN108385187A (en
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王丽丽
邵义伟
李晓林
赵艳丽
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Jiangsu Hengli Chemical Fiber Co Ltd
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    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/78—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
    • D01F6/84—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from copolyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16—Dicarboxylic acids and dihydroxy compounds
    • C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/181—Acids containing aromatic rings
    • C08G63/183—Terephthalic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/78—Preparation processes
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/04—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers
    • D01F11/08—Chemical after-treatment of artificial filaments or the like during manufacture of synthetic polymers of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds

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  • General Chemical & Material Sciences (AREA)
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  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
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  • Polymers & Plastics (AREA)
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Abstract

The invention relates to a high-strength airplane safety belt and a preparation method thereof, wherein modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare high-strength polyester industrial yarn, and then the high-strength airplane safety belt is prepared through weaving, wherein an oiling agent for oiling contains crown ether with the content of 67.30-85.58 wt%, and when the oiling agent is used, water is used for preparing emulsion with the concentration of 10-20 wt%. The preparation method is simple, the material of the prepared high-strength polyester industrial yarn is modified polyester with molecular chains comprising terephthalic acid chain segments, ethylene glycol chain segments and dihydric alcohol chain segments with branched chains, and the structural formula of the dihydric alcohol chain with the branched chains is as follows:
Figure DDA0001508768710000011
in the formula, R1And R2Each independently selected from linear alkylene having 1 to 3 carbon atoms, R3Selected from alkyl with 1-5 carbon atoms, R4And (3) alkyl with 2-5 carbon atoms is selected, and the tensile load value of the finally prepared high-strength airplane safety belt is more than or equal to 14700N.

Description

High-strength airplane safety belt and preparation method thereof
Technical Field
The invention belongs to the field of fiber preparation, and relates to a high-strength airplane safety belt and a preparation method thereof.
Background
Polyethylene terephthalate (PET) is a polymer with excellent performance, and the PET has the advantages of high modulus, high strength, good shape retention, good barrier property and the like, so that the PET is widely applied to the fields of fibers, bottle packaging, films, sheets and the like, the yield is increased year by year, and the industrial position is remarkably improved.
However, in the polycondensation reaction for synthesizing ethylene terephthalate, especially in the case of linear high polymer, linear and cyclic oligomers are also associated due to high-temperature oxidative degradation, the cyclic oligomers are formed by the back-biting cyclization of the chain ends of macromolecules in the polycondensation stage, about 70% or more of the cyclic oligomers are cyclic trimers, and the cyclic trimers have the characteristics of easy aggregation, easy crystallization, high chemical and heat stability and the like, and the formation of the cyclic trimers has the following influence on the processing of polyester: (1) the spinning assembly can be blocked, and the service life of the melt filter and the assembly is influenced; (2) the fiber can be separated out in the process of heat setting and deposited on a heating roller, so that the friction force is increased and the heating is uneven; (3) the dyeing process takes the cyclic trimer as a center, so that the dye is gathered and adhered to the surface of the fiber, the phenomena of dye color points, spots, color flowers and the like appear on the surface of the fiber, the hand feeling and the color light of the fabric woven by the fiber are influenced, and meanwhile, the normal liquid flow velocity of a melt is limited by the cyclic oligomer filled with a pipeline and a valve, so that the fiber is unevenly dyed, and the reproducibility is poor; (4) the adhesive is adhered to the surface of the fiber, so that the winding is difficult, the phenomena of yarn breakage, uneven thickness and the like occur, the mechanical properties of the fiber such as breaking strength, breaking elongation and the like are influenced, and the product quality is seriously influenced. With the increasing production of polyester fiber, the demand for polyester quality is increasing, so the problem of polyester post-processing caused by cyclic oligomer is attracting attention, especially with the rapid development of fine denier polyester fiber, the market puts higher demands on the dyeing of polyester fiber. In order to reduce the generation of cyclic oligomers in the polycondensation reaction of polyesters, researchers at home and abroad have conducted a great deal of research. The main methods for reducing cyclic oligomers in polyesters are: (1) pentavalent phosphorus compound or ether compound is added to combine with metal catalyst in the polyester synthesis process, or the amount of heat stabilizer is increased, so as to generate stabilization effect on polyester, and thus the generation of cyclic trimer can be inhibited under high temperature melting; (2) the residence time of the polyester melt at high temperature is reduced. However, the above-mentioned method causes a decrease in the molecular weight and a broadening of the distribution of the polyester, affecting the quality of the finally obtained fiber, while the effect of reducing the cyclic trimer oligomers is not significant.
Because most PET fibers have small dielectric constant, low moisture regain and high friction coefficient, a spin finish must be used in the spinning process. The main component of the oil agent is surfactant, and can form directional adsorption layer, i.e. oil film, on the surface of chemical fibre, on one hand, the hydrophilic group of the oil film is oriented to space, and can adsorb moisture in the air, and on the fibre surface a continuous water film can be formed, so that the charged ions can be migrated on the surface of the fibre, and the accumulation of static charge produced by friction between the fibres can be reduced, so that the surface resistance of the fibre can be reduced, and the conductivity of fibre can be raised, on the other hand, the oil film isolating fibre can produce a certain affinity for fibre, and can make it possess a certain concentration property and do not scatter, and in addition, the oil film also can give fibre a certain smoothness, so that the fibre can not be damaged in the course of friction, and has good hand feeling, and can smoothly pass through the operation procedures of winding, drawing and drying, etc. when spinning, the electrostatic action in the course of textile processing can be eliminated, and the, The roller, the cylinder and other adverse phenomena reduce the generation of broken filaments and broken ends, and ensure the quality of fiber products. The friction behavior of the fiber can be changed after the oil film on the surface of the fiber is broken at high temperature, high speed and certain pressure, so that the friction force is increased, and other problems such as broken filaments and broken ends of the fiber are caused. Along with the development of high speed, super high speed and multifunctional fiber of polyester filament, the development of an oil solution with good heat resistance, low viscosity, high oil film strength, good smoothness and strong antistatic property is of great practical significance.
The high-strength polyester industrial yarn has wide application and can be used in the fields of safety belts, conveyor belts and the like. But the preparation of the high-strength polyester industrial yarn at the present stage has two main problems, namely, the oil agent is quick to volatilize and easy to bond on the surface of the fiber, so that the prepared fiber has high unevenness rate and poor performance; secondly, the volatile residue of oligomer in the fiber is on the surface of the spinneret plate, which causes fiber broken filaments and influences the quality of the fiber.
Therefore, how to provide a high strength fiber with uniform spinning and low oligomer content is a problem to be solved.
Disclosure of Invention
The invention aims to solve the problems that in the prior art, the fiber quality is influenced by uneven fiber and excessive residual oligomer in a spinneret plate due to the fact that an oiling agent is fast in volatilization and easy to adhere to the surface of the fiber, and provides a high-strength airplane safety belt with uniform spinning and low oligomer content and a preparation method thereof. The introduction of the dihydric alcohol with the branched chain in the modified polyester reduces the cyclic oligomer generated in the polyester side reaction and improves the quality of the fiber; the crown ether-containing oil agent is used, so that the heat resistance and the lubricity of the oil agent are improved, the quality of fibers is improved, and the crown ether has lower viscosity and higher volatile point than a conventional smoothing agent, so that the friction coefficient of the crown ether-containing oil agent is smaller, and the crown ether-containing oil agent has more excellent heat-resistant stability, thereby improving the processability of the fibers and reducing the occurrence of a broken filament phenomenon;
in order to achieve the purpose, the invention adopts the technical scheme that:
the high-strength airplane safety belt is formed by weaving high-strength polyester industrial yarns, the high-strength polyester industrial yarns are made of modified polyester, a molecular chain of the modified polyester comprises a terephthalic acid chain segment, an ethylene glycol chain segment and a dihydric alcohol chain segment with a branched chain, and the structural formula of the dihydric alcohol with the branched chain is as follows:
Figure GDA0001695686480000031
in the formula, R1And R2Each independently selected from linear alkylene having 1 to 3 carbon atoms, R3Selected from alkyl with 1-5 carbon atoms, R4The carbon atom number is 2-5, and the purpose of carbon atom number limitation is as follows: because a branched chain structure and a long chain structure are introduced into the dihydric alcohol, the electronegativity of an alkoxy part is weakened, the number of carbon atoms of the branched chain structure is too small, the electronegativity influence on the alkoxy part is small, and the significance for reducing the generation of cyclic oligomers is not large; the too large number of carbon atoms of the branched chain structure can generate intermolecular entanglement and influence the distribution of molecular weight;
the tensile load value of the high-strength airplane safety belt is more than or equal to 14700N.
As a preferred technical scheme:
the high-strength airplane safety belt has the advantages that the fineness of the high-strength polyester industrial yarn is 1100-1670 dtex, the deviation rate of linear density is-1.2-1.5%, the breaking strength is not less than 8.1cN/dtex, the breaking strength CV value is not more than 2.0%, the central value of elongation at break is 14.0%, the deviation rate of elongation at break is +/-1.0%, the CV value of elongation at break is not more than 6.0%, the central value of elongation at 4.0cN/dtex load is 5.5-6.2%, the deviation rate of elongation at 4.0cN/dtex load is +/-0.8%, the dry heat shrinkage rate under the conditions of 177 ℃, 10min and 0.05cN/dtex is 6.0-9.5%, the network is 3-9 pieces/m, and the oil content is 0.35-0.8%. Therefore, the polyester industrial yarn prepared by the invention has high breaking strength and good uniformity.
According to the high-strength airplane safety belt, the content of the cyclic oligomer in the modified polyester is less than or equal to 0.6 wt%, the amount of the cyclic oligomer in the polyester prepared by the prior art is 1.5-2.1 wt%, and compared with the prior art, the generation amount of the cyclic oligomer is remarkably reduced;
the number average molecular weight of the modified polyester is 20000-27000, the molecular weight distribution index is 1.8-2.2, the molecular weight of the modified polyester is higher, the molecular weight distribution is narrower, the spinning processing requirement can be met, and the preparation of fibers with excellent performance is facilitated;
the molar content of the dihydric alcohol chain segment with the branched chain in the modified polyester is 3-5% of that of the terephthalic acid chain segment, and the molar content of the dihydric alcohol chain segment with the branched chain in the modified polyester is lower, so that the excellent performance of the polyester is maintained;
the dihydric alcohol with a branch chain is 2-ethyl-2-methyl-1, 3-propanediol, 2-diethyl-1, 3-propanediol, 2-butyl-2-ethyl-1, 3-propanediol, 3-diethyl-1, 5-pentanediol, 4-diethyl-1, 7-heptanediol, 4-di (1, -methylethyl) -1, 7-heptanediol, 3-dipropyl-1, 5-pentanediol, 4-dipropyl-1, 7-heptanediol, 4-methyl-4- (1, 1-dimethylethyl) -1, 7-heptanediol, 3-methyl-3-pentyl-1, 6-hexanediol or 3, 3-dipentyl-1, 5-pentanediol.
The preparation method of the modified polyester for the high-strength airplane safety belt comprises the following steps: uniformly mixing terephthalic acid, ethylene glycol and the dihydric alcohol with the branched chain, and then carrying out esterification reaction and polycondensation reaction in sequence to obtain the modified polyester.
The high-strength airplane safety belt comprises the following specific preparation steps of:
(1) performing esterification reaction;
preparing terephthalic acid, ethylene glycol and the dihydric alcohol with the branched chain into slurry, adding a catalyst and a stabilizer, uniformly mixing, pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is normal pressure to 0.3MPa, the esterification reaction temperature is 250-260 ℃, and the esterification reaction endpoint is determined when the distilled amount of water in the esterification reaction reaches more than 90% of a theoretical value;
(2) performing polycondensation reaction;
and after the esterification reaction is finished, starting the polycondensation reaction in a low vacuum stage under the negative pressure condition, stably pumping the pressure in the low vacuum stage from normal pressure to below 500Pa in 30-50 min at the reaction temperature of 260-270 ℃ for 30-50 min, then continuously pumping the vacuum to perform the polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to below 100Pa, controlling the reaction temperature to 275-285 ℃ and the reaction time to be 50-90 min, and thus obtaining the modified polyester.
The high-strength airplane safety belt is characterized in that in the step (1), the molar ratio of terephthalic acid, ethylene glycol and the branched diol is 1: 1.2-2.0: 0.03-0.06, the addition amount of the catalyst is 0.01-0.05% of the weight of the terephthalic acid, and the addition amount of the stabilizer is 0.01-0.05% of the weight of the terephthalic acid;
the catalyst is antimony trioxide, ethylene glycol antimony or antimony acetate, and the stabilizer is triphenyl phosphate, trimethyl phosphate or trimethyl phosphite.
The invention also provides a method for preparing the high-strength airplane safety belt, which comprises the steps of tackifying the modified polyester through solid phase polycondensation, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare high-strength polyester industrial yarns, and weaving the high-strength polyester industrial yarns to prepare the high-strength airplane safety belt;
the oil agent for oiling contains crown ether, the content of the crown ether is 67.30-85.58 wt%, the content of the crown ether in the oil agent needs to be kept within a certain range, the oil agent with low viscosity, good heat resistance and high oil film strength cannot be prepared if the addition amount of the crown ether is too low, and other performance indexes of the oil agent can be influenced if the addition amount of the crown ether is too high.
Crown ethers are heterocyclic organic compounds containing a plurality of ether groups. The wetting ability of the crown ether surfactant is larger than that of a corresponding open-chain compound, the crown ether has better solubilization, the solubility of the salt compound in the organic compound is lower, but the solubility of the organic matter of the salt compound is improved along with the addition of the crown ether. The common polyester compounds or polyethers in the oil agent have larger intermolecular action due to larger molecular weight and the action of hydrogen bonds, and show larger kinematic viscosity, and after the crown ether is added, the crown ether can be well compatible in the polyester compounds or polyether oil agent system, enters between polyester compounds or polyether molecular chains, shields the acting force between the molecular chains, and thus the viscosity of the oil agent system is reduced. Meanwhile, the antistatic agent of the chemical fiber oiling agent is mainly divided into anionic surfactant, cationic surfactant and amphoteric surfactant, most of which contain metal ions or exist in the form of salt, so that the compatibility of the antistatic agent and polyester compounds or polyethers in the oiling agent is ensured, and the addition of the crown ether improves the compatibility of the antistatic agent and the polyester compounds or polyethers due to the salt dissolution effect, thereby improving the strength of an oiling agent oil film and having great significance on the stability of spinning and the product holding capacity. Indexes of the oil agent are reflected by a comprehensive factor, so that a certain restriction is provided for the addition amount of crown ether, the advantages of heat resistance and oil film strength of the oil agent are not reflected sufficiently due to too low amount, and other indexes are limited;
when the oil agent is used, water is used to prepare an emulsion with the concentration of 10-20 wt%.
As a preferred technical scheme:
the method is characterized in that the intrinsic viscosity of the modified polyester after solid-phase polycondensation and tackifying is 1.0-1.2 dL/g; the intrinsic viscosity is a representation mode of molecular weight, the intrinsic viscosity is too high, the subsequent processing temperature is increased, and the product is easy to be thermally degraded; if the intrinsic viscosity is too low, the required strength and performance are difficult to achieve;
after the oil agent is heated and treated at 200 ℃ for 2 hours, the thermal weight loss is less than 15 wt%, the crown ether has a higher volatile point and excellent heat-resistant stability, and the heat-resistant performance of the oil agent introduced with the crown ether is also remarkably improved;
the kinematic viscosity of the oil agent is 27.5-30.1 mm at the temperature of (50 +/-0.01) ° C2The kinematic viscosity of the oil agent prepared from water into 10 wt% emulsion is 0.93-0.95 mm2The crown ether can reduce the viscosity of the oil agent mainly because the crown ether has lower viscosity and is a bead-shaped micromolecule, and after the crown ether is introduced into the oil agent system, the crown ether can be well compatible in the polyester compound or polyether compound oil agent system and simultaneously enters between molecular chains of the polyester compound or polyether compound to shield the acting force between the molecular chains, so that the viscosity of the oil agent system is reduced;
the oil film strength of the oil agent is 121-127N, the oil film strength of the oil agent in the prior art is low and is generally about 110N, the main reason is that most of antistatic agents of the chemical fiber oil agent contain metal ions or exist in the form of salt, the compatibility of the antistatic agents and polyester compounds or polyether compounds in the oil agent is poor, and the crown ether can improve the oil film strength is mainly that salt solution effect can be generated after the crown ether is added, so that the compatibility of the antistatic agents and the polyester compounds or polyether compounds is improved, and the oil film strength of the oil agent is further improved;
the surface tension of the oil agent is 23.2-26.8 cN/cm, and the specific resistance is 1.0 x 108～1.8×108Ω·cm；
After oiling, the static friction coefficient between the fibers is 0.250-0.263, and the dynamic friction coefficient is 0.262-0.273;
after oiling, the static friction coefficient between the fiber and the metal is 0.202-0.210, and the dynamic friction coefficient is 0.320-0.332.
The crown ether is 2-hydroxymethyl-12-crown-4, 15-crown ether-5 or 2-hydroxymethyl-15-crown-5;
the oil agent also contains mineral oil, phosphate potassium salt, trimethylolpropane laurate and alkyl sodium sulfonate;
the mineral oil is one of 9# to 17# mineral oil;
the phosphate potassium salt is dodecyl phosphate potassium salt, isomeric tridecanol polyoxyethylene ether phosphate potassium salt or dodecatetradecanol phosphate potassium salt;
the sodium alkyl sulfonate is sodium dodecyl sulfonate, sodium pentadecyl sulfonate or sodium hexadecyl sulfonate;
the preparation method of the oil agent comprises the following steps: uniformly mixing crown ether, phosphate potassium salt, trimethylolpropane laurate and sodium alkyl sulfonate, adding the mixture into mineral oil, and uniformly stirring to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight:
Figure GDA0001695686480000061
the mixing is carried out at normal temperature, the stirring temperature is 40-55 ℃, and the stirring time is 1-3 h.
The spinning process parameters of the high-strength polyester industrial yarn are as follows:
the spinning temperature is 295 ℃;
the process parameters of the post heater are as follows:
the length is 300-400 mm; the temperature is 310-330 ℃;
the technological parameters of the cooling air are as follows:
the pressure is 700-850 Pa; the temperature is 20-25 ℃;
the humidity is 75-85%; the wind speed is 0.4-0.6 m/s;
the technological parameters of stretching and heat setting are as follows:
Figure GDA0001695686480000062
the invention mechanism is as follows:
the method comprises the steps of firstly preparing modified polyester comprising a terephthalic acid chain segment, an ethylene glycol chain segment and a dihydric alcohol chain segment with a branched chain, then carrying out solid-phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding on the modified polyester to obtain the high-strength polyester industrial yarn, weaving the high-strength polyester industrial yarn to obtain the high-strength airplane safety belt, wherein an oiling agent for oiling contains crown ether, the content of the crown ether is 67.30-85.58 wt%, and the influence of the synergistic effect of the modified polyester and the oiling agent on the performance of the finally prepared high-strength airplane safety belt is as follows:
the addition of the modified polyester reduces the generation of cyclic oligomer, prolongs the service life of the assembly, improves the spinning stability and improves the uniformity of the fiber. In addition, the invention also adopts the oil agent containing crown ether, which increases the stability of spinning, and improves the stability of spinning by cooperating with the modified polyester, thereby improving the quality of fiber.
In organic compounds, the angle between two chemical bonds formed by the same atom in a molecule is called the bond angle, which is usually expressed in degrees, and the electronegativity of the central atom and the coordinating atom in the molecule of the organic compound affects the bond angle of the molecule. When the electronegativity of the coordinating atom bonded to the central atom is increased, the electron-withdrawing ability of the coordinating atom is increased, the bonding electron pair moves toward the ligand and is farther away from the central atom, so that the bond pairs are closer to each other due to the decrease in repulsive force, and the bond angle is decreased, and conversely, when the electronegativity of the coordinating atom bonded to the central atom is decreased, the electron-donating ability of the coordinating atom is increased, the bonding electron pair moves toward the central atom and is closer to the central atom, so that the bond pairs are farther away from each other due to the increase in repulsive force, and the bond angle is increased.
According to Pauling electronegativity scale, the electronegativity of C, H and O atoms are 2.55, 2.20 and 3.44, respectively, and according to valence electron energy equilibrium theory, the calculation formula of the group electronegativity is shown as follows:
Figure GDA0001695686480000071
in the formula, xiIs the electronegativity of the neutral atom of the i atom before bonding, Nve,iIs the number of valence electrons in the i atom, niIs the number of i atoms in the molecule. The calculation steps for the electronegativity of more complex groups are mainly: the electronegativity of the simple group is firstly calculated, then the electronegativity of the more complex group is calculated by taking the simple group as a quasi atom, and the electronegativity of the target group is finally obtained through successive iteration. In calculating the electronegativity of a quasi-atom, the valence electron that is not bonded in a radical atom (for example, the radical atom of a group-OH is an O atom) is regarded as the valence electron of the quasi-atom.
In the invention, C atoms are combined with O atoms of hydroxyl groups in dihydric alcohol to form new C-O bonds in ester groups after C-O bonds of carboxyl groups in terephthalic acid are broken, bond angles between C-C bonds formed by the C atoms in the ester groups and C atoms on a benzene ring and the newly formed chemical bonds C-O are recorded as α, the change of the bond angle α influences the ring forming reaction, when α is less than 109 ℃, molecules are easy to form rings, and the ring forming probability of the molecules is reduced along with the increase of α.
Figure GDA0001695686480000072
In the formula, R1And R2Each independently selected from linear alkylene having 1 to 3 carbon atoms, R3Selected from alkyl with 1-5 carbon atoms, R4Selected from alkyl with 2-5 carbon atoms. The diol structure is introduced with a branched chain structure and a long chain structure, so that the electronegativity of an alkoxy part of the diol structure is weakened, and the electronegativity of a group connected with a carbonyl group in diacid in the diol structure is 2.59-2.79 according to a calculation formula of the electronegativity of the group, and a group-OCH (OCH) group connected with the carbonyl group in the diacid in ethylene glycol2CH2Electronegativity of-was 3.04, so that the alkoxy group was in comparison with-OCH in ethylene glycol2CH2Having a stronger electron donating property, so that the bond-forming electron pairs on the newly formed chemical bond C-O bond will move towards the central C atom, closer to the central atom, away from each other due to the increased repulsion, and further away from each otherThe bond angle α is larger than 109 degrees, the probability of generating linear polymer is increased, thereby reducing the generation of cyclic oligomer, being beneficial to reducing the phenomena of broken filaments, uneven thickness and the like, being beneficial to reducing the influence on the mechanical properties of fibers such as breaking strength, breaking elongation and the like, and further improving the product quality.
The crown ether is introduced into the oil agent to prepare the oil agent with low viscosity, good heat resistance and higher oil film strength. In the prior art, the higher viscosity of the oil agent is mainly due to the fact that the oil agent contains a common polyester compound or polyether compound, the intermolecular action of the compound is larger due to the larger molecular weight and the action of hydrogen bonds, the kinematic viscosity is larger, so that the viscosity of the oil agent is higher, the viscosity of the oil agent can be obviously reduced after crown ether is added, the crown ether is mainly due to the fact that the viscosity of the crown ether is lower and is bead-shaped micromolecule, the crown ether can be well compatible in a polyester compound or polyether oil agent system and simultaneously enters between molecular chains of the polyester compound or polyether compound to shield acting force between the molecular chains, and therefore the viscosity of the oil agent system is reduced. In the prior art, the oil film strength of the oil agent is low mainly because the antistatic agent of the chemical fiber oil agent mostly contains metal ions or exists in the form of salt, so that the compatibility of the antistatic agent and polyester compounds or polyethers in the oil agent is poor, and the crown ether can improve the oil film strength mainly because the crown ether can generate a salt solution effect after being added, so that the compatibility of the antistatic agent and the polyester compounds or polyethers is improved, and the oil film strength of the oil agent is further improved. In addition, the crown ether has a higher volatile point and excellent heat-resistant stability, the heat-resistant performance of the oil agent introduced with the crown ether is also obviously improved, and the processing performance of the fiber is improved because the crown ether has lower viscosity, a higher volatile point, a smaller friction coefficient and excellent heat-resistant stability.
Has the advantages that:
(1) the high-strength airplane safety belt and the preparation method thereof have simple and reasonable preparation process, and the high-strength airplane safety belt prepared from the high-strength polyester industrial yarn has high tensile property and high breaking strength;
(2) according to the preparation method of the high-strength airplane safety belt, the dihydric alcohol with the branched chain is introduced into the modified polyester, so that the bond angle of polyester molecules is changed, and the generation of cyclic oligomers in the polyester synthesis process is remarkably reduced;
(3) according to the preparation method of the high-strength airplane safety belt, the oiling agent containing the crown ether used in the oiling process has the characteristics of low viscosity, good heat resistance, high oil film strength, good smoothness and strong antistatic property, and the spinning stability and the fiber processability are improved.
Detailed Description
The invention will be further illustrated with reference to specific embodiments. It should be understood that these examples are for illustrative purposes only and are not intended to limit the scope of the present invention. Further, it should be understood that various changes or modifications of the present invention may be made by those skilled in the art after reading the teaching of the present invention, and such equivalents may fall within the scope of the present invention as defined in the appended claims.
Example 1
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 2-ethyl-2-methyl-1, 3-propanediol with a molar ratio of 1:1.2:0.03 into slurry, adding antimony trioxide and triphenyl phosphate, uniformly mixing, pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is normal pressure, the esterification reaction temperature is 250 ℃, and the esterification reaction end point is when the distilled amount of water in the esterification reaction reaches 90% of a theoretical value, wherein the adding amount of the antimony trioxide is 0.01% of the weight of the terephthalic acid, the adding amount of the triphenyl phosphate is 0.05% of the weight of the terephthalic acid, and the structural formula of the 2-ethyl-2-methyl-1, 3-propanediol is as follows:
Figure GDA0001695686480000091
(b) performing polycondensation reaction; after the esterification reaction is finished, starting the polycondensation reaction in the low vacuum stage under the condition of negative pressure, smoothly pumping the pressure from normal pressure to the absolute pressure of 500Pa within 30min, controlling the reaction temperature to be 260 ℃ and the reaction time to be 40min, then continuing to pump the vacuum, and carrying out the polycondensation reaction in the high vacuum stage to further reduce the reaction pressure to the absolute pressure of 100Pa, control the reaction temperature to be 275 ℃ and control the reaction time to be 70min, thus obtaining the modified polyester. Wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, a glycol chain segment and a 2-ethyl-2-methyl-1, 3-propanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.6 wt%, the number average molecular weight is 20000, the molecular weight distribution index is 2.0, and the molar content of the 2-ethyl-2-methyl-1, 3-propanediol chain segment in the modified polyester is 3% of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-12-crown-4 with dodecyl phosphate potassium salt, trimethylolpropane laurate and sodium dodecyl sulfate at normal temperature, adding into No. 9 mineral oil, and uniformly stirring at 40 ℃ for 1h to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 2 parts of No. 9 mineral oil; 10 parts of trimethylolpropane laurate; 2-hydroxymethyl-12-crown-490 parts; 8 parts of dodecyl phosphate potassium salt; and 3 parts of sodium dodecyl sulfate. The content of crown ether in the prepared oil agent is 79.6 wt%, the high temperature resistance of the oil agent is excellent, and the thermal weight loss is 14.5 wt% after the oil agent is heated for 2 hours at 200 ℃; the viscosity of the oil agent is low, and the kinematic viscosity is 29.6mm at the temperature of (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.93mm after preparation with water as an emulsion having a concentration of 10% by weight2S; the oil agent has high oil film strength of 125N, surface tension of 24.8cN/cm, and specific resistance of 1.3 × 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.255, coefficient of dynamic friction (. mu.)d) 0.266, coefficient of static friction (. mu.) between fiber and metal (F/M)s) 0.203, coefficient of dynamic friction (. mu.)d) 0.320, and the prepared oil agent is prepared into an emulsion with the concentration of 15 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 32000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.0dL/g, and the replacement period of the spinning assembly is 40 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 2
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 2, 2-diethyl-1, 3-propanediol with a molar ratio of 1:1.3:0.04 into slurry, adding ethylene glycol antimony and trimethyl phosphate, uniformly mixing, and pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is normal pressure, the esterification reaction temperature is 260 ℃, and the esterification reaction end point is when the water distillation amount in the esterification reaction reaches 91% of a theoretical value, wherein the adding amount of the ethylene glycol antimony is 0.02% of the weight of the terephthalic acid, the adding amount of the trimethyl phosphate is 0.03% of the weight of the terephthalic acid, and the structural formula of the 2, 2-diethyl-1, 3-propanediol is as follows:
Figure GDA0001695686480000101
(b) performing polycondensation reaction; after the esterification reaction is finished, starting the polycondensation reaction in the low vacuum stage under the condition of negative pressure, smoothly pumping the pressure from normal pressure to absolute pressure of 490Pa within 35min, controlling the reaction temperature to 261 ℃ and the reaction time to 30min, then continuing to pump the vacuum, and carrying out the polycondensation reaction in the high vacuum stage, so that the reaction pressure is further reduced to absolute pressure of 100Pa, the reaction temperature is 277 ℃ and the reaction time is 85min, thus obtaining the modified polyester. Wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, a glycol chain segment and a 2, 2-diethyl-1, 3-propanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.6 wt%, the number average molecular weight is 27000, the molecular weight distribution index is 1.8, and the molar content of the 2, 2-diethyl-1, 3-propanediol chain segment in the modified polyester is 5% of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 15-crown ether-5, isotridecanol polyoxyethylene ether phosphate potassium salt, trimethylolpropane laurate and sodium pentadecylsulfonate at normal temperature, adding into 10# mineral oil, and uniformly stirring at 43 ℃ for 1.5h to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 2 parts of No. 10 mineral oil; 15 parts of trimethylolpropane laurate; 15-crown ether-570 parts; 10 parts of isomeric tridecanol polyoxyethylene ether phosphate potassium salt; and 7 parts of sodium pentadecylsulfonate. The prepared oil agent has crown ether content of 67.30 wt%, excellent high temperature resistance, thermal weight loss of 13 wt% after heating treatment at 200 deg.C for 2h, low viscosity, and kinematic viscosity of 28.1mm at (50 + -0.01) ° C2(s) a kinematic viscosity of 0.93mm after preparation with water as an emulsion having a concentration of 10% by weight2(s) 123N, which is a high oil film strength of the oil, 25.1cN/cm, which is a surface tension of the oil, and 1.5X 10 of specific resistance8Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.257, coefficient of dynamic friction (. mu.)d) 0.265, coefficient of static friction (. mu.m) between fiber and metal (F/M) after oilings) 0.205, coefficient of dynamic friction (. mu.)d) 0.323, the prepared oil agent is prepared into emulsion with the concentration of 10 wt% by water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 38000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.08dL/g, and the replacement period of the spinning assembly is 42 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 3
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 2-butyl-2-ethyl-1, 3-propanediol with a molar ratio of 1:1.4:0.05 into slurry, adding antimony acetate and trimethyl phosphite, uniformly mixing, and then pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is 0.1MPa, the esterification reaction temperature is 252 ℃, the esterification reaction end point is when the distilled water amount in the esterification reaction reaches 92% of a theoretical value, the adding amount of the antimony acetate is 0.03% of the weight of the terephthalic acid, the adding amount of the trimethyl phosphite is 0.01% of the weight of the terephthalic acid, and the structural formula of the 2-butyl-2-ethyl-1, 3-propanediol is as follows:
Figure GDA0001695686480000111
(b) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is smoothly pumped from normal pressure to the absolute pressure of 495Pa within 40min, the reaction temperature is 263 ℃, the reaction time is 45min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 95Pa absolute, 278 ℃ reaction temperature and 60min reaction time, preparing modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, a glycol chain segment and a 2-butyl-2-ethyl-1, 3-propanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.5 wt%, the number average molecular weight is 21000, the molecular weight distribution index is 2.2, and the molar content of the 2-butyl-2-ethyl-1, 3-propanediol chain segment in the modified polyester is 4% of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-15-crown-5 with potassium dodecatetradecanol phosphate, trimethylolpropane laurate and sodium pentadecylsulfonate at normal temperature, adding into No. 11 mineral oil, and uniformly stirring at 48 ℃ for 3h to obtain an oil solution; the addition amount of each component is as follows according to the parts by weight: 8 parts of No. 11 mineral oil; 10 parts of trimethylolpropane laurate; 2-hydroxymethyl-15-crown-585 parts; 11 parts of potassium dodecatetradecanol phosphate; 5 parts of sodium pentadecylsulfonate. Of crown ethers in the preparationThe content is 70.83 wt%, the high temperature resistance of the oil agent is excellent, the thermal weight loss is 11 wt% after the oil agent is heated and treated for 2 hours at 200 ℃, the viscosity of the oil agent is lower, and the kinematic viscosity is 30.1mm at the temperature of (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.94mm after preparation with water as an emulsion having a concentration of 10% by weight2The oil film strength of the oil agent is higher and is 125N. The surface tension of the oil agent was 23.2cN/cm, and the specific resistance was 1.8X 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.250, coefficient of dynamic friction (. mu.)d) 0.272, coefficient of static friction (. mu.) between fiber and metal (F/M) after oilings) 0.209, coefficient of dynamic friction (. mu.)d) 0.329, and the prepared oil agent is prepared into an emulsion with the concentration of 15 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 30000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation tackifying is 1.10dL/g, and the replacement period of the spinning assembly is 48 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 4
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 3, 3-diethyl-1, 5-pentanediol; reacting 3, 3-diethyl-propionaldehyde, acetaldehyde and triethylamine for 20min at 90 ℃ under nitrogen atmosphere, adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, cooling after the reaction is finished, separating out the catalyst, treating the solution with ion exchange resin, evaporating water under reduced pressure, separating and purifying to obtain 3, 3-diethyl-1, 5-pentanediol, wherein the structural formula of the 3, 3-diethyl-1, 5-pentanediol is as follows:
Figure GDA0001695686480000121
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 3, 3-diethyl-1, 5-pentanediol with the molar ratio of 1:1.5:0.06 into slurry, adding antimony trioxide and triphenyl phosphate, uniformly mixing, pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is 0.3MPa, the temperature of the esterification reaction is 255 ℃, and the end point of the esterification reaction is determined when the distilled amount of water in the esterification reaction reaches 95% of a theoretical value, wherein the adding amount of the antimony trioxide is 0.04% of the weight of the terephthalic acid, and the adding amount of the triphenyl phosphate is 0.01% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is stably pumped from normal pressure to the absolute pressure of 400Pa within 50min, the reaction temperature is 265 ℃, the reaction time is 33min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 90Pa absolute, the reaction temperature is 280 ℃, the reaction time is 50min, preparing modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, an ethylene glycol chain segment and a 3, 3-diethyl-1, 5-pentanediol chain segment, the content of cyclic oligomers in the modified polyester is 0.2 wt%, the number average molecular weight is 23000, the molecular weight distribution index is 1.9, and the molar content of the 3, 3-diethyl-1, 5-pentanediol chain segment in the modified polyester is 3.5% of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-12-crown-4 with dodecyl phosphate potassium salt, trimethylolpropane laurate and sodium hexadecylsulfonate at normal temperature, adding into 12# mineral oil, and uniformly stirring at 40 ℃ for 2.5h to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 5 parts of No. 12 mineral oil; 2-hydroxymethyl-12-crown-495 parts; 9 parts of dodecyl phosphate potassium salt; and 2 parts of sodium hexadecyl sulfonate. The prepared oil agent has crown ether content of 85.58 wt%, excellent high temperature resistance, thermal weight loss of 9 wt% after heating treatment at 200 deg.C for 2h, low viscosity, and kinematic viscosity of 29.5mm at (50 + -0.01) ° C2S, usingThe kinematic viscosity of water after preparation of an emulsion with a concentration of 10% by weight is 0.93mm2(s) the oil film strength of the oil agent is high and is 121N, the surface tension of the oil agent is 24.3cN/cm, and the specific resistance is 1.0X 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.260, coefficient of dynamic friction (. mu.)d) 0.263, coefficient of static friction (. mu.m) between fiber and metal (F/M) after oilings) 0.202, coefficient of dynamic friction (. mu.)d) 0.330, and the prepared oil agent is prepared into emulsion with the concentration of 18 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 33000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.13dL/g, and the replacement period of the spinning assembly is 44 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 5
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 4, 4-diethyl-1, 7-heptanediol; reacting 4, 4-diethyl-butyraldehyde, propionaldehyde and triethylamine for 20min at 92 ℃ under nitrogen atmosphere, then adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, cooling after the reaction is finished, separating out the catalyst, treating the solution with ion exchange resin, evaporating water under reduced pressure, separating and purifying to obtain 4, 4-diethyl-1, 7-heptanediol, wherein the structural formula of the 4, 4-diethyl-1, 7-heptanediol is as follows:
Figure GDA0001695686480000131
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 4, 4-diethyl-1, 7-heptanediol with a molar ratio of 1:1.6:0.03 into slurry, adding ethylene glycol antimony and trimethyl phosphate, uniformly mixing, and pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is normal pressure, the esterification reaction temperature is 257 ℃, and the esterification reaction end point is when the water distillation amount in the esterification reaction reaches 92% of a theoretical value, wherein the adding amount of the ethylene glycol antimony is 0.05% of the weight of the terephthalic acid, and the adding amount of the trimethyl phosphate is 0.04% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is stably pumped from normal pressure to the absolute pressure of 450Pa within 33min, the reaction temperature is 270 ℃, the reaction time is 30min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 95Pa absolute, the reaction temperature to 275 ℃, and the reaction time to 60min to obtain modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, a glycol chain segment and a 4, 4-diethyl-1, 7-heptanediol chain segment, the content of cyclic oligomers in the modified polyester is 0.5 wt%, the number average molecular weight is 25000, the molecular weight distribution index is 2.1, and the molar content of the 4, 4-diethyl-1, 7-heptanediol chain segment in the modified polyester is 5% of the molar content of the terephthalic acid chain segment.
(2) Preparing an oiling agent; uniformly mixing 15-crown ether-5, isotridecanol polyoxyethylene ether phosphate potassium salt, trimethylolpropane laurate and sodium dodecyl sulfate at normal temperature, adding into 13# mineral oil, and uniformly stirring at 52 ℃ for 2 hours to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 10 parts of No. 13 mineral oil; 5 parts of trimethylolpropane laurate; 15-crown ether-570 parts; 8 parts of isomeric tridecanol polyoxyethylene ether phosphate potassium salt; 6 parts of sodium dodecyl sulfate. The prepared oil agent has crown ether content of 70.70 wt%, excellent high temperature resistance, thermal weight loss of 13.5 wt% after heating treatment at 200 ℃ for 2h, low viscosity of the oil agent, and kinematic viscosity of 28.6mm at (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.95mm after preparation with water as an emulsion having a concentration of 10% by weight2(s) 126N, which is a high oil film strength of the oil agent, and the surface tension of the oil agentThe force was 24.9cN/cm and the specific resistance was 1.2X 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.251, coefficient of dynamic friction (. mu.)d) 0.262, coefficient of static friction (. mu.m) between fiber and metal (F/M) after oilings) 0.202, coefficient of dynamic friction (. mu.)d) 0.332, and the prepared oil agent is prepared into an emulsion with the concentration of 20 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 35000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.07dL/g, and the replacement period of the spinning assembly is 49 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 6
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 4, 4-di (1-methylethyl) -1, 7-heptanediol; reacting 4, 4-bis (1-methylethyl) -butyraldehyde, propionaldehyde and triethylamine for 20min at 95 ℃ under nitrogen atmosphere, adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, and cooling to separate out the catalyst after the reaction. After the solution is treated by ion exchange resin, water is evaporated under reduced pressure, and the 4, 4-di (1-methylethyl) -1, 7-heptanediol is separated and purified, wherein the structural formula of the 4, 4-di (1-methylethyl) -1, 7-heptanediol is as follows:
Figure GDA0001695686480000151
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 4, 4-di (1-methylethyl) -1, 7-heptanediol with the molar ratio of 1:1.7:0.05 into slurry, adding antimony acetate and trimethyl phosphite, uniformly mixing, and pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is 0.2MPa, the temperature of the esterification reaction is 253 ℃, and the end point of the esterification reaction is determined when the distilled amount of water in the esterification reaction reaches 96% of a theoretical value, wherein the adding amount of the antimony acetate is 0.01% of the weight of the terephthalic acid, and the adding amount of the trimethyl phosphite is 0.05% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is stably pumped from normal pressure to the absolute pressure of 480Pa within 38min, the reaction temperature is 262 ℃, the reaction time is 38min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 98Pa absolute, the reaction temperature to 279 ℃, and the reaction time to 80min to obtain modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, a glycol chain segment and a 4, 4-di (1-methylethyl) -1, 7-heptanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.55 wt%, the number average molecular weight is 27000, the molecular weight distribution index is 2.2, and the molar content of the 4, 4-di (1-methylethyl) -1, 7-heptanediol chain segment in the modified polyester is 4% of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-15-crown-5 with potassium dodecatetradecanol phosphate, trimethylolpropane laurate and sodium pentadecylsulfonate at normal temperature, adding into 14# mineral oil, and uniformly stirring at 55 ℃ for 1h to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 3 parts of No. 14 mineral oil; 10 parts of trimethylolpropane laurate; 2-hydroxymethyl-15-crown-575 parts; 14 parts of potassium dodecatetradecanol phosphate; and 7 parts of sodium pentadecylsulfonate. The prepared oil agent has the crown ether content of 68.80 wt%, excellent high temperature resistance, thermal weight loss of 12 wt% after heat treatment at 200 ℃ for 2h, low viscosity, and kinematic viscosity of 27.5mm at (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.95mm after preparation with water as an emulsion having a concentration of 10% by weight2The oil film strength of the oil agent was 126N. The surface tension of the oil agent was 25.4cN/cm, and the specific resistance was 1.6X 108Omega cm, after oiling, fiber andcoefficient of static friction (. mu.) between fibers (F/F)s) 0.255, coefficient of dynamic friction (. mu.)d) 0.267, coefficient of static friction (. mu.) between fiber and metal (F/M) after oilings) 0.203, coefficient of dynamic friction (. mu.)d) 0.330, and the prepared oil agent is prepared into 16 wt% emulsion by water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 31000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation tackifying is 1.08dL/g, and the replacement period of the spinning assembly is 40 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 7
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 3, 3-dipropyl-1, 5-pentanediol; reacting 3, 3-dipropyl-propionaldehyde, acetaldehyde and triethylamine for 20min at 94 ℃ in nitrogen atmosphere, adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, cooling after the reaction is finished, and separating out the catalyst. After the solution is treated by ion exchange resin, water is evaporated under reduced pressure, and the 3, 3-dipropyl-1, 5-pentanediol is separated and purified, wherein the structural formula of the 3, 3-dipropyl-1, 5-pentanediol is as follows:
Figure GDA0001695686480000161
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 3, 3-dipropyl-1, 5-pentanediol with the molar ratio of 1:1.8:0.03 into slurry, adding antimony trioxide and triphenyl phosphate, uniformly mixing, and pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is 0.3MPa, the esterification reaction temperature is 250 ℃, and the esterification reaction end point is the end point of the esterification reaction when the distilled amount of water in the esterification reaction reaches 90% of a theoretical value, wherein the adding amount of the antimony trioxide is 0.03% of the weight of the terephthalic acid, and the adding amount of the triphenyl phosphate is 0.02% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is smoothly pumped from normal pressure to the absolute pressure of 455Pa within 42min, the reaction temperature is 264 ℃, the reaction time is 45min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 85Pa absolute, the reaction temperature to 285 ℃, the reaction time to 75min, preparing modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, an ethylene glycol chain segment and a 3, 3-dipropyl-1, 5-pentanediol chain segment, the content of cyclic oligomers in the modified polyester is 0.45 wt%, the number average molecular weight is 26500, the molecular weight distribution index is 2.2, and the molar content of the 3, 3-dipropyl-1, 5-pentanediol chain segment in the modified polyester is 4.5% of the molar content of the terephthalic acid chain segment.
(2) Preparing an oiling agent; uniformly mixing 15-crown ether-5 with dodecyl phosphate potassium salt, trimethylolpropane laurate and sodium hexadecylsulfonate at normal temperature, adding the mixture into 15# mineral oil, and uniformly stirring the mixture for 2 hours at 41 ℃ to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 8 parts of No. 15 mineral oil; 20 parts of trimethylolpropane laurate; 15-crown ether-5100 parts; 15 parts of dodecyl phosphate potassium salt; and 2 parts of sodium hexadecyl sulfonate. The prepared oil agent has the crown ether content of 68.97 wt%, excellent high temperature resistance, thermal weight loss of 8.5 wt% after 2h of heat treatment at 200 ℃, low viscosity of the oil agent, and kinematic viscosity of 28.4mm at (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.94mm after preparation with water as an emulsion having a concentration of 10% by weight2The oil film strength of the oil agent was high and was 122N. The surface tension of the oil agent was 26.8cN/cm, and the specific resistance was 1.8X 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.263, coefficient of dynamic friction (. mu.)d) 0.268, coefficient of static friction (. mu.M) between fiber and metal (F/M) after oilings) 0.210, coefficient of dynamic friction (. mu.)d) 0.320, and the prepared oil agent is prepared into an emulsion with the concentration of 17 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 35000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.2dL/g, and the replacement period of the spinning assembly is 41 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 8
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 4, 4-dipropyl-1, 7-heptanediol; reacting 4, 4-dipropyl-butyraldehyde, acetaldehyde and triethylamine for 20min at 92 ℃ in nitrogen atmosphere, adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, cooling after the reaction is finished, and separating out the catalyst. Treating the solution with ion exchange resin, evaporating water under reduced pressure, separating, and purifying to obtain 4, 4-dipropyl-1, 7-heptanediol, wherein the structural formula of the 4, 4-dipropyl-1, 7-heptanediol is as follows:
Figure GDA0001695686480000171
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 4, 4-dipropyl-1, 7-heptanediol with the molar ratio of 1:1.9:0.04 into slurry, adding ethylene glycol antimony and trimethyl phosphate, uniformly mixing, pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is 0.3MPa, the esterification reaction temperature is 260 ℃, and the esterification reaction end point is the end point when the distilled amount of water in the esterification reaction reaches 93% of a theoretical value, wherein the adding amount of the ethylene glycol antimony is 0.04% of the weight of the terephthalic acid, and the adding amount of the trimethyl phosphate is 0.03% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is stably pumped from normal pressure to the absolute pressure of 475Pa within 45min, the reaction temperature is 265 ℃, the reaction time is 48min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 88Pa absolute, 283 ℃ reaction temperature, and 80min reaction time to obtain modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, a glycol chain segment and a 4, 4-dipropyl-1, 7-heptanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.6 wt%, the number average molecular weight is 23000, the molecular weight distribution index is 2.0, and the molar content of the 4, 4-dipropyl-1, 7-heptanediol chain segment in the modified polyester is 3% of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-12-crown-4 with potassium dodecatetradecanol phosphate, trimethylolpropane laurate and sodium pentadecylsulfonate at normal temperature, adding into 16# mineral oil, and uniformly stirring at 45 ℃ for 3h to obtain an oil solution; the addition amount of each component is as follows according to the parts by weight: 9 parts of No. 16 mineral oil; 2-hydroxymethyl-12-crown-480 parts; 12 parts of potassium dodecatetradecanol phosphate; 5 parts of sodium pentadecylsulfonate. The prepared oil agent has crown ether content of 83.33 wt%, excellent high temperature resistance, thermal weight loss of 14 wt% after heating treatment at 200 deg.C for 2h, low viscosity of the oil agent, and kinematic viscosity of 30.0mm at (50 + -0.01) ° C2(s) a kinematic viscosity of 0.93mm after preparation with water as an emulsion having a concentration of 10% by weight2The oil film strength of the oil agent was 127N. The surface tension of the oil agent was 23.5cN/cm, and the specific resistance was 1.5X 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.262, coefficient of dynamic friction (. mu.)d) 0.273, coefficient of static friction (. mu.M) between fiber and metal (F/M) after oilings) 0.208, coefficient of dynamic friction (. mu.)d) 0.328, and the prepared oil agent is prepared into emulsion with the concentration of 18 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 30000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.15dL/g, and the replacement period of the spinning assembly is 44 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 9
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 4-methyl-4- (1, 1-dimethylethyl) -1, 7-heptanediol; reacting 4-methyl-4- (1, 1-dimethylethyl) -butyraldehyde, propionaldehyde and triethylamine for 20min at 92 ℃ under nitrogen atmosphere, then adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, cooling after the reaction is finished, separating the catalyst out, treating the solution with ion exchange resin, evaporating water under reduced pressure, separating and purifying to obtain 4-methyl-4- (1, 1-dimethylethyl) -1, 7-heptanediol, wherein the structural formula of the 4-methyl-4- (1, 1-dimethylethyl) -1, 7-heptanediol is as follows:
Figure GDA0001695686480000191
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 4-methyl-4- (1, 1-dimethylethyl) -1, 7-heptanediol with the molar ratio of 1:2.0:0.05 into slurry, adding antimony acetate and trimethyl phosphate, uniformly mixing, pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is normal pressure MPa, the esterification reaction temperature is 251 ℃, and the esterification reaction end point is determined when the water distillation amount in the esterification reaction reaches 96% of a theoretical value, wherein the adding amount of the antimony acetate is 0.05% of the weight of the terephthalic acid, and the adding amount of the trimethyl phosphate is 0.04% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, starting the polycondensation reaction in the low vacuum stage under the condition of negative pressure, smoothly pumping the pressure from normal pressure to the absolute pressure of 420Pa within 30min, the reaction temperature is 267 ℃, the reaction time is 50min, then continuing to pump the vacuum, carrying out the polycondensation reaction in the high vacuum stage, further reducing the reaction pressure to the absolute pressure of 80Pa, the reaction temperature is 280 ℃, and the reaction time is 90min, thus obtaining the modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, a glycol chain segment and a 4-methyl-4- (1, 1-dimethylethyl) -1, 7-heptanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.25 wt%, the number average molecular weight is 24000, the molecular weight distribution index is 2.2, and the 4-methyl-4- (1, 1-dimethylethyl) -1 in the modified polyester, the molar content of the 7-heptanediol chain segment is 4 percent of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-15-crown-5 with dodecyl phosphate potassium salt, trimethylolpropane laurate and sodium dodecyl sulfate at normal temperature, and uniformly stirring at 55 ℃ for 3 hours to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 15 parts of trimethylolpropane laurate; 2-hydroxymethyl-15-crown-590 parts; 8 parts of dodecyl phosphate potassium salt; 7 parts of sodium dodecyl sulfate. The prepared oil agent has the crown ether content of 81.81 wt%, excellent high temperature resistance, thermal weight loss of 10 wt% after heating treatment at 200 ℃ for 2h, low viscosity of the oil agent, and kinematic viscosity of 29.7mm at (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.94mm after preparation with water as an emulsion having a concentration of 10% by weight2The oil film strength of the oil agent was 126N. The surface tension of the oil agent was 24.8cN/cm, and the specific resistance was 1.8X 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.250, coefficient of dynamic friction (. mu.)d) 0.264, coefficient of static friction (. mu.m) between fiber and metal (F/M) after oilings) 0.210, coefficient of dynamic friction (. mu.)d) 0.321, and the prepared oil agent is prepared into an emulsion with the concentration of 11 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fiber number is 30000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation tackifying is 1.0dL/g, and the replacement period of the spinning assembly is 45 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 10
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 3-methyl-3-pentyl-1, 6-hexanediol; reacting 3-methyl-3-pentyl-propionaldehyde, propionaldehyde and triethylamine for 20min at 90 ℃ under a nitrogen atmosphere, adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, and cooling to separate out the catalyst after the reaction is finished. After the solution is treated by ion exchange resin, water is evaporated under reduced pressure, and the 3-methyl-3-pentyl-1, 6-hexanediol is obtained through separation and purification, wherein the structural formula of the 3-methyl-3-pentyl-1, 6-hexanediol is as follows:
Figure GDA0001695686480000201
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 3-methyl-3-pentyl-1, 6-hexanediol with a molar ratio of 1:1.2:0.06 into slurry, adding ethylene glycol antimony and trimethyl phosphite, uniformly mixing, and pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is 0.1MPa, the esterification reaction temperature is 255 ℃, and the esterification reaction end point is the end point when the distilled water amount in the esterification reaction reaches 92% of a theoretical value, wherein the adding amount of the ethylene glycol antimony is 0.01% of the weight of the terephthalic acid, and the adding amount of the trimethyl phosphite is 0.01% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is stably pumped from normal pressure to the absolute pressure of 490Pa within 50min, the reaction temperature is 269 ℃, the reaction time is 30min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 100Pa absolute, the reaction temperature to 281 ℃, the reaction time to 55min, preparing modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, an ethylene glycol chain segment and a 3-methyl-3-amyl-1, 6-hexanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.1 wt%, the number average molecular weight is 20000, the molecular weight distribution index is 1.9, and the molar content of the 3-methyl-3-amyl-1, 6-hexanediol chain segment in the modified polyester is 3.5 percent of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-15-crown-5 with dodecyl phosphate potassium salt, trimethylolpropane laurate and sodium dodecyl sulfate at normal temperature, and uniformly stirring at 55 ℃ for 3 hours to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 15 parts of trimethylolpropane laurate; 2-hydroxymethyl-15-crown-590 parts; 8 parts of dodecyl phosphate potassium salt; 7 parts of sodium dodecyl sulfate. The prepared oil agent has the crown ether content of 81.81 wt%, excellent high temperature resistance, thermal weight loss of 10 wt% after heating treatment at 200 ℃ for 2h, low viscosity of the oil agent, and kinematic viscosity of 29.7mm at (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.94mm after preparation with water as an emulsion having a concentration of 10% by weight2(s) 126N, which is a high oil film strength of the oil agent, 24.8cN/cm, which is a surface tension of the oil agent, and 1.8X 10 which is a specific resistance8Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.250, coefficient of dynamic friction (. mu.)d) 0.264, coefficient of static friction (. mu.m) between fiber and metal (F/M) after oilings) 0.210, coefficient of dynamic friction (. mu.)d) 0.321, preparing the prepared oil agent into an emulsion with the concentration of 12 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein, the maximum ply fiber number is 33000dtex when ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.1dL/g, and the replacement period of the spinning assembly is 42 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
Example 11
The preparation method of the high-strength airplane safety belt comprises the following specific steps:
(1) preparing modified polyester:
(a) preparing 3, 3-diamyl-1, 5-pentanediol; reacting 3, 3-diamyl-propionaldehyde, acetaldehyde and triethylamine for 20min at 95 ℃ under nitrogen atmosphere, adding the concentrated solution into a hydrogenation reactor with a Raney nickel catalyst, reacting at the hydrogen pressure of 2.914MPa and the temperature of 100 ℃, and cooling to separate out the catalyst after the reaction is finished. After the solution is treated by ion exchange resin, water is evaporated under reduced pressure, and the 3, 3-diamyl-1, 5-pentanediol is obtained by separation and purification, wherein the structural formula of the 3, 3-diamyl-1, 5-pentanediol is as follows:
Figure GDA0001695686480000211
(b) performing esterification reaction; preparing terephthalic acid, ethylene glycol and 3, 3-diamyl-1, 5-pentanediol with the molar ratio of 1:2.0:0.03 into slurry, adding antimony acetate and trimethyl phosphite, uniformly mixing, and pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is 0.2MPa, the esterification reaction temperature is 250 ℃, and the esterification reaction end point is determined when the distilled amount of water in the esterification reaction reaches 97% of a theoretical value, wherein the adding amount of the antimony acetate is 0.01% of the weight of the terephthalic acid, and the adding amount of the trimethyl phosphite is 0.05% of the weight of the terephthalic acid;
(c) performing polycondensation reaction; after the esterification reaction is finished, the polycondensation reaction in the low vacuum stage is started under the condition of negative pressure, the pressure is stably pumped from normal pressure to the absolute pressure of 500Pa within 45min, the reaction temperature is 260 ℃, the reaction time is 40min, then continuously vacuumizing, carrying out polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to 92Pa absolute, the reaction temperature to 277 ℃, reacting for 80min, preparing modified polyester, wherein the molecular chain of the modified polyester comprises a terephthalic acid chain segment, an ethylene glycol chain segment and a 3, 3-diamyl-1, 5-pentanediol chain segment, the content of cyclic oligomer in the modified polyester is 0.35 wt%, the number average molecular weight is 25500, the molecular weight distribution index is 1.8, and the molar content of the 3, 3-diamyl-1, 5-pentanediol chain segment in the modified polyester is 5 percent of the molar content of the terephthalic acid chain segment;
(2) preparing an oiling agent; uniformly mixing 2-hydroxymethyl-12-crown-4 with dodecyl phosphate potassium salt, trimethylolpropane laurate and sodium dodecyl sulfate at normal temperature, adding into No. 9 mineral oil, and uniformly stirring at 40 ℃ for 1h to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight: 2 parts of No. 9 mineral oil; 10 parts of trimethylolpropane laurate; 2-hydroxymethyl-12-crown-490 parts; 8 parts of dodecyl phosphate potassium salt; and 3 parts of sodium dodecyl sulfate. The prepared oil agent has crown ether content of 79.6 wt%, excellent high temperature resistance, thermal weight loss of 14.5 wt% after heating treatment at 200 ℃ for 2h, low viscosity of the oil agent, and kinematic viscosity of 29.6mm at (50 +/-0.01) ° C2(s) a kinematic viscosity of 0.93mm after preparation with water as an emulsion having a concentration of 10% by weight2(s) the oil has high oil film strength of 125N, surface tension of 24.8cN/cm, and specific resistance of 1.3X 108Omega cm, coefficient of static friction (mu) between fibres (F/F) after oilings) 0.255, coefficient of dynamic friction (. mu.)d) 0.266, after oiling, the coefficient of static friction (μ) between fiber and metal (F/M)s) 0.203, coefficient of dynamic friction (. mu.)d) 0.320, and the prepared oil agent is prepared into an emulsion with the concentration of 15 wt% by using water when in use;
(3) the modified polyester is subjected to solid phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding to prepare the high-strength polyester industrial yarn, and the high-strength polyester industrial yarn is woven to prepare the high-strength airplane safety belt. Wherein the maximum ply fineness is 37000dtex during ply twisting, the intrinsic viscosity of the modified polyester after solid phase polycondensation and tackifying is 1.2dL/g, and the replacement period of the spinning assembly is 47 days.
The spinning process parameters of the high-strength polyester industrial yarn are shown in table 1.
The high-strength polyester industrial yarn and various performance parameters of the finally prepared high-strength airplane safety belt are shown in a table 2.
TABLE 1
Figure GDA0001695686480000221
Figure GDA0001695686480000231
Figure GDA0001695686480000241
TABLE 2
Note: in Table 2, A represents the central value (%) of the elongation at a load of 4.0cN/dtex for the high-tenacity polyester industrial yarn, B represents the deviation (%) of the elongation at a load of 4.0cN/dtex for the high-tenacity polyester industrial yarn, and C represents the dry heat shrinkage (%) under the conditions of 10min and 0.05 cN/dtex.
Figure GDA0001695686480000242
Figure GDA0001695686480000251

Claims (10)

1. The preparation method of the high-strength airplane safety belt is characterized in that the high-strength airplane safety belt is prepared by carrying out solid-phase polycondensation tackifying, melting, metering, extruding, cooling, oiling, stretching, heat setting and winding on modified polyester;
the molecular chain of the modified polyester comprises a terephthalic acid chain segment, an ethylene glycol chain segment and a dihydric alcohol chain segment with a branched chain, wherein the structural formula of the dihydric alcohol with the branched chain is as follows:
Figure FDA0002398132130000011
in the formula, R1And R2Each independently selected from linear alkylene having 1 to 3 carbon atoms, R3Selected from alkyl with 1-5 carbon atoms, R4Selected from alkyl with 2-5 carbon atoms;
the oiling oil agent contains crown ether, and the content of the crown ether is 67.30-85.58 wt%;
the crown ether is 2-hydroxymethyl-12-crown-4, 15-crown ether-5 or 2-hydroxymethyl-15-crown-5;
when the oil agent is used, preparing an emulsion with the concentration of 10-20 wt% by using water;
the content of cyclic oligomer in the modified polyester is less than or equal to 0.6 wt%;
the modified polyester has a number average molecular weight of 20000 to 27000 and a molecular weight distribution index of 1.8 to 2.2;
the molar content of the dihydric alcohol chain segment with the branched chain in the modified polyester is 3-5% of that of the terephthalic acid chain segment.
2. The method for preparing the high-strength airplane safety belt according to claim 1, wherein the intrinsic viscosity of the modified polyester after solid-phase polycondensation and tackifying is 1.0-1.2 dL/g;
the thermal weight loss of the oil agent after heating treatment for 2 hours at 200 ℃ is less than 15 wt%;
the kinematic viscosity of the oil agent is 27.5-30.1 mm at the temperature of (50 +/-0.01) ° C2The kinematic viscosity of the oil agent prepared from water into 10 wt% emulsion is 0.93-0.95 mm2/s；
The oil film strength of the oil agent is 121-127N;
the surface tension of the oil agent is 23.2-26.8 cN/cm, and the specific resistance is 1.0 x 108～1.8×108Ω·cm；
After oiling, the static friction coefficient between the fibers is 0.250-0.263, and the dynamic friction coefficient is 0.262-0.273;
after oiling, the static friction coefficient between the fiber and the metal is 0.202-0.210, and the dynamic friction coefficient is 0.320-0.332;
the oil agent also contains mineral oil, phosphate potassium salt, trimethylolpropane laurate and alkyl sodium sulfonate;
the mineral oil is one of 9# to 17# mineral oil;
the phosphate potassium salt is dodecyl phosphate potassium salt, isomeric tridecanol polyoxyethylene ether phosphate potassium salt or dodecatetradecanol phosphate potassium salt;
the sodium alkyl sulfonate is sodium dodecyl sulfonate, sodium pentadecyl sulfonate or sodium hexadecyl sulfonate.
3. The preparation method of the high-strength airplane safety belt according to claim 2, wherein the preparation method of the oil agent comprises the following steps: uniformly mixing crown ether, phosphate potassium salt, trimethylolpropane laurate and sodium alkyl sulfonate, adding the mixture into mineral oil, and uniformly stirring to obtain an oil agent; the addition amount of each component is as follows according to the parts by weight:
Figure FDA0002398132130000021
the mixing is carried out at normal temperature, the stirring temperature is 40-55 ℃, and the stirring time is 1-3 h.
4. The method for preparing the high-strength airplane safety belt according to claim 3, wherein the spinning process parameters of the high-strength polyester industrial yarn are as follows:
the spinning temperature is 295 ℃;
the process parameters of the post heater are as follows:
the length is 300-400 mm; the temperature is 310-330 ℃;
the technological parameters of the cooling air are as follows:
the pressure is 700-850 Pa; the temperature is 20-25 ℃;
the humidity is 75-85%; the wind speed is 0.4-0.6 m/s;
the technological parameters of stretching and heat setting are as follows:
Figure FDA0002398132130000022
5. the method for preparing a high-strength airplane safety belt according to claim 1, wherein the method comprises the following steps: the high-strength airplane safety belt is woven by high-strength polyester industrial yarns, the high-strength polyester industrial yarns are made of modified polyester, and the tensile load value of the high-strength airplane safety belt is more than or equal to 14700N.
6. The method for preparing a high-strength airplane safety belt according to claim 5, wherein the fineness of the high-strength polyester industrial yarn is 1100 to 1670dtex, the deviation rate of linear density is-1.2 to 1.5%, the breaking strength is more than or equal to 8.1cN/dtex, the breaking strength CV value is less than or equal to 2.0%, the central value of the breaking elongation is 14.0%, the deviation rate of the breaking elongation is +/-1.0%, the breaking elongation CV value is less than or equal to 6.0%, the central value of the elongation of 4.0cN/dtex load is 5.5 to 6.2%, the deviation rate of the elongation of 4.0cN/dtex load is +/-0.8%, the dry heat shrinkage rate under the conditions of 177 ℃, 10min and 0.05cN/dtex is 6.0 to 9.5%, the network is 3 to 9/m, and the oil content is 0.35 to 0.8%.
7. The method for producing a high-strength airplane safety belt according to claim 5 or 6, wherein the branched diol is 2-ethyl-2-methyl-1, 3-propanediol, 2-diethyl-1, 3-propanediol, 2-butyl-2-ethyl-1, 3-propanediol, 3-diethyl-1, 5-pentanediol, 4-diethyl-1, 7-heptanediol, 4-bis (1, -methylethyl) -1, 7-heptanediol, 3-dipropyl-1, 5-pentanediol, 4-dipropyl-1, 7-heptanediol, 4-methyl-4- (1, 1-dimethylethyl) -1, 7-heptanediol, 3-methyl-3-pentyl-1, 6-hexanediol or 3, 3-diamyl-1, 5-pentanediol.
8. The method for preparing the high-strength airplane safety belt according to claim 7, wherein the modified polyester is prepared by the following steps: uniformly mixing terephthalic acid, ethylene glycol and the dihydric alcohol with the branched chain, and then carrying out esterification reaction and polycondensation reaction in sequence to obtain the modified polyester.
9. The method for preparing the high-strength airplane safety belt according to claim 8, wherein the modified polyester is prepared by the following specific steps:
(1) performing esterification reaction;
preparing terephthalic acid, ethylene glycol and the dihydric alcohol with the branched chain into slurry, adding a catalyst and a stabilizer, uniformly mixing, pressurizing in a nitrogen atmosphere to perform esterification reaction, wherein the pressurizing pressure is normal pressure to 0.3MPa, the esterification reaction temperature is 250-260 ℃, and the esterification reaction endpoint is determined when the distilled amount of water in the esterification reaction reaches more than 90% of a theoretical value;
(2) performing polycondensation reaction;
and after the esterification reaction is finished, starting the polycondensation reaction in a low vacuum stage under the negative pressure condition, stably pumping the pressure in the low vacuum stage from normal pressure to below 500Pa in 30-50 min at the reaction temperature of 260-270 ℃ for 30-50 min, then continuously pumping the vacuum to perform the polycondensation reaction in a high vacuum stage, further reducing the reaction pressure to below 100Pa, controlling the reaction temperature to 275-285 ℃ and the reaction time to be 50-90 min, and thus obtaining the modified polyester.
10. The method for preparing the high-strength airplane safety belt according to claim 9, wherein in the step (1), the molar ratio of the terephthalic acid to the ethylene glycol to the branched diol is 1: 1.2-2.0: 0.03-0.06, the addition amount of the catalyst is 0.01-0.05% of the weight of the terephthalic acid, and the addition amount of the stabilizer is 0.01-0.05% of the weight of the terephthalic acid;
the catalyst is antimony trioxide, ethylene glycol antimony or antimony acetate, and the stabilizer is triphenyl phosphate, trimethyl phosphate or trimethyl phosphite.
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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101392416A (en) * 2008-10-29 2009-03-25 泉州至和织造有限公司 Improved polyester monofilament production method
CN105019244A (en) * 2015-07-31 2015-11-04 江苏恒科新材料有限公司 High-strength polyester filament fiber and preparation method thereof
CN105463608A (en) * 2015-12-29 2016-04-06 江苏恒力化纤股份有限公司 High-strength safety belt polyester industrial yarn and preparation method thereof
CN106381557A (en) * 2016-08-31 2017-02-08 江苏恒力化纤股份有限公司 High-uniformity polyester industrial yarn used for safety belt and production method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101392416A (en) * 2008-10-29 2009-03-25 泉州至和织造有限公司 Improved polyester monofilament production method
CN105019244A (en) * 2015-07-31 2015-11-04 江苏恒科新材料有限公司 High-strength polyester filament fiber and preparation method thereof
CN105463608A (en) * 2015-12-29 2016-04-06 江苏恒力化纤股份有限公司 High-strength safety belt polyester industrial yarn and preparation method thereof
CN106381557A (en) * 2016-08-31 2017-02-08 江苏恒力化纤股份有限公司 High-uniformity polyester industrial yarn used for safety belt and production method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
一种冠醚化合物作为新型润滑油添加剂的抗磨减摩性能研究;张俊彦等;《摩擦学学报》;19990930;第19卷(第3期);第278-280页 *

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