Preparation and Properties of PED-TDI Polyurethane-Modified Silicone Coatings

To explore the influence mechanisms of polyurethane soft segments on modified silicone coatings, a series of modified coatings was prepared by introducing different contents of hydroxypropyl-terminated polydimethylsiloxane (PDMS2200) into the soft segment of polyurethane. ATR-FTIR, NMR, CLSM, AFM, contact angle measurement, the tensile test, bacterial adhesion, and the benthic diatom adhesion test were used to investigate the structure, morphology, roughness, degree of microphase separation, surface energy, tensile properties, and antifouling properties of the modified coatings. The results show that PDMS2200 could aggravate the microphase separation of the modified coatings, increase the surface-free energy, and reduce its elastic modulus; when the microphase separation exceeded a certain degree, increasing PDMS2200 would decrease the tensile properties. The PED-TDI polyurethane-modified silicone coating prepared with the formula of PU-Si17 had the best tensile properties and antifouling properties among all modified coatings.


Introduction
Marine biofouling is a serious problem that ships cannot avoid, which is mainly caused by the adsorption and growth of marine organisms, such as bacteria and diatoms, on the hull's surface [1,2]. The existence of these organisms will not only increase the roughness of the hull, thereby increasing the fuel consumption and limiting the speed of the ship, but also facilitate biological invasion [3,4].
Among all antifouling methods, fouling-release antifouling coatings that can achieve excellent antifouling effects without biocides have great advantages [5][6][7]. They prevent the adhesion of fouling organisms by providing a smooth surface with low friction and low surface-free energy. Even if adsorption is successful, the adhesion between the organisms and the coating is so weak that the fouling could be easily removed by the water stress or mechanical cleaning.
Currently, fouling-release antifouling coatings include organic fluorine coatings and silicone coatings. The latter have lower marine organism adhesion strength and cost [8]. What is more, silicone coatings also have great chemical stability and low glass transition temperature, making them widely used in ship antifouling. However, silicone coatings also have some shortcomings, such as low mechanical strength [9,10], poor adhesion to the substrate [11], and poor static antifouling effects [5,12]. Therefore, they need to be modified to meet the needs during the actual use process.
Common modified materials mainly include alkyd resin, epoxy resin, acrylic resin, and polyurethane [13][14][15][16]. With its good mechanical properties and adhesion, polyurethane can well improve the defects of silicone coatings [17], so it is an excellent modified material. Furthermore, there are two modification methods: physical blending, and chemical modification. The former is easy to operate; yet some segments will be broken before stretching due to the poor compatibility between silicone and polyurethane [18]. Therefore, it is difficult to apply in practical applications; the preparation of the latter is cumbersome, Silicone-modified polyurethane prepolymers were prepared by selecting PED, PET, PDMS2200, and TDI as reaction monomers. After using BDO to extend the chain, the isocyanate-terminated PED-TDI polyurethane was obtained. The reaction principle is shown in Figure 1.
BDO) was 1:4.5. A series of polyurethanes was prepared by gradually increasing the percentage of PDMS2200 (XPDMS) in the soft segment. The mole percentages of th segment raw materials are shown in Table 1. Silicone-modified polyurethane prepolymers were prepared by selecting PED PDMS2200, and TDI as reaction monomers. After using BDO to extend the chain, th cyanate-terminated PED-TDI polyurethane was obtained. The reaction principle is s in Figure 1.

Synthesis Principle of Modified Organic Silicone Resin
A polyurethane-modified silicone coating that can be cross-linked and cured at temperature was prepared in the ratio of DY-107:silicone-modified polyurethane:eth thosilicate:catalyst = 20:5:4:0.5. The reaction principle involved is shown in Figure 2

Synthesis Principle of Modified Organic Silicone Resin
A polyurethane-modified silicone coating that can be cross-linked and cured at room temperature was prepared in the ratio of DY-107:silicone-modified polyurethane:ethyl orthosilicate:catalyst = 20:5:4:0.5. The reaction principle involved is shown in Figure 2.

Preparation Process
By referring to the relevant literature [28], the reaction scheme was determined as follows: Firstly, a four-neck flask was connected to the SZCL-2A digital intelligent control magnetic stirrer (Yuhua Instrument Co., Ltd., Gongyi, China). At the same time, polyol, PDMS2200, and 60 g mixed solvent (consisting of 40 wt.% dimethyl benzene, 40 wt.% butyl acetate, and 20 wt.% cyclohexanone) were added at the proportion shown in Table 1. Under the protection of N2, the rotating speed of the magnetic stirrer was controlled to be 160 r/min, and the reaction system was heated to 50 °C by using a DF-101 constant temperature heating magnetic stirrer (China Gongyi Yuhua Instrument Co., Ltd.), and then TDI was added dropwise. After stirring for 30 min, the reaction system was heated to 80 °C. After reacting for 2 h, the reaction system was air-cooled to 50 °C, and 2.6 g BDO was added. After that, the system was heated to 75 °C for a 4 h chain expansion reaction, and polyurethane prepolymer was finally obtained. The specific device is shown in Figure 3a.

Preparation Process
By referring to the relevant literature [28], the reaction scheme was determined as follows: Firstly, a four-neck flask was connected to the SZCL-2A digital intelligent control magnetic stirrer (Yuhua Instrument Co., Ltd., Gongyi, China). At the same time, polyol, PDMS2200, and 60 g mixed solvent (consisting of 40 wt.% dimethyl benzene, 40 wt.% butyl acetate, and 20 wt.% cyclohexanone) were added at the proportion shown in Table 1. Under the protection of N 2 , the rotating speed of the magnetic stirrer was controlled to be 160 r/min, and the reaction system was heated to 50 • C by using a DF-101 constant temperature heating magnetic stirrer (China Gongyi Yuhua Instrument Co., Ltd.), and then TDI was added dropwise. After stirring for 30 min, the reaction system was heated to 80 • C. After reacting for 2 h, the reaction system was air-cooled to 50 • C, and 2.6 g BDO was added. After that, the system was heated to 75 • C for a 4 h chain expansion reaction, and polyurethane prepolymer was finally obtained. The specific device is shown in Figure 3a.
PED-TDI polyurethane was added to DY-107 in the proportion shown above, and ethyl orthosilicate and catalyst were successively added. The modified silicone coating was obtained after 20 min of reaction. The process is shown in Figure 3b. The modified products were coated in glass slides and PTFE molds, respectively, and a series of glass slides and mold samples were obtained by crosslinking curing at room temperature. The former was used for structural characterization, surface and interface performance testing, antifouling performance testing, etc. The latter was used for tensile performance testing. perature heating magnetic stirrer (China Gongyi Yuhua Instrument Co., Ltd.), and th TDI was added dropwise. After stirring for 30 min, the reaction system was heated to °C. After reacting for 2 h, the reaction system was air-cooled to 50 °C, and 2.6 g BDO w added. After that, the system was heated to 75 °C for a 4 h chain expansion reaction, an polyurethane prepolymer was finally obtained. The specific device is shown in Figure 3

Chemical Structure
Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR, Thermo Fisher Scientific Inc., Waltham, MA, USA) was used to determine functional groups of polyurethane and modified silicone coatings. The scanning range was 4000-650 cm −1 , the resolution was 2 cm −1 , and the number of scans was 32 times.
Nuclear magnetic resonance spectrometer (NMR, Bruker 400M, Bruker Physik-Ag, Karlsruhe, Germany) was used to determine the hydrogen spectra of polyurethane prepolymers and modified organosilicon coatings. The resonance frequency was 400 MHz, and the solvent was CDCl 3 .

Surface Observation
Confocal laser scanning microscopy (CLSM, OLS4000, Olympus, Tokyo, Japan) was used to observe the surface of the modified silicone coating. The roughness was calculated by the LEXT analysis software.
Atomic force microscopy (AFM, Bruker Dimension Icon, Bruker Physik-AG, Karlsruhe, Germany) was used to observe the microphase separation on the surface of modified coatings. The probe type was OTESPA-R3, and the scanning mode was Tapping. The scanning frequency was 1 Hz, and the scanning pixel was 256.
A JC2000C contact angle measurement instrument (Zhongchen Digital Technology Equipment Co., Ltd., Shanghai, China) was used to measure the modified coatings' water and diiodomethane contact angle, and the surface energy γ of the modified coatings was calculated by Owens's two-liquid method [29].

Tensile Test
A UTM 5105 computer-controlled electronic universal testing machine (Jinan Wance Electrical Equipment Co., Ltd., Jinan, China) was used to test the casting sample at a tensile rate of 50 mm/min, and the elastic modulus, elongation, and fracture strength were calculated according to the stress-strain curves.

Antifouling Evaluation
Bacterial adhesion and benthic diatom tests were carried out on the modified coatings. The antifouling properties of the modified coatings were measured by comparing the bacterial adhesion rate and chlorophyll content on the coating surface. The specific steps are shown in the literature [30,31].

Chemical Structure
The preparation of the modified coatings mainly involves the reaction between hydroxyl and isocyanate. To verify whether the modification is successful, the polyurethane (denoted by P) and its modified coatings (denoted by C) were tested by ATR-FTIR. The results are shown in Figure 4.  For the modified coatings, the characteristic peaks corresponding to the -NCO groups disappeared, indicating that the free isocyanate groups in the polyurethane have been wholly consumed. At the same time, the characteristic peaks corresponding to Si-CH3 groups and Si-O-Si groups in the modified coatings were significantly enhanced which was caused by the addition of a large amount of silicone resin in the subsequen experiments.
To further analyze the chemical structure of the polyurethane and the modified coat ings, their NMR spectra were tested, and the results are shown in Figure 5.
C-PED-TDI P-PED-TDI For the modified coatings, the characteristic peaks corresponding to the -NCO groups disappeared, indicating that the free isocyanate groups in the polyurethane have been wholly consumed. At the same time, the characteristic peaks corresponding to Si-CH 3 groups and Si-O-Si groups in the modified coatings were significantly enhanced, which was caused by the addition of a large amount of silicone resin in the subsequent experiments.
To further analyze the chemical structure of the polyurethane and the modified coatings, their NMR spectra were tested, and the results are shown in Figure 5.
The chemical shift near 0 ppm corresponded to the proton on the Si-CH 3 group. The chemical shift at δ = 0.79-1.48 ppm was attributed to hydrogen on methylene groups linked to Si in PDMS2200. The chemical shift around 1.7 ppm corresponded to the methyl group on TDI. The chemical shift at δ = 2.0-2.5 ppm was attributed to methyl and methylene groups on PED and PET. The chemical shift at δ = 3.5 ppm corresponded to hydrogen on methyne linked to carbamate; the multiple signal peaks near 4.0 ppm were attributed to the protons in methylene on PDMS2200. Combined with ATR-FTIR spectra, it could be determined that polyurethane-modified silicone coatings were successfully prepared. been wholly consumed. At the same time, the characteristic peaks corresponding CH3 groups and Si-O-Si groups in the modified coatings were significantly enh which was caused by the addition of a large amount of silicone resin in the subs experiments.
To further analyze the chemical structure of the polyurethane and the modifie ings, their NMR spectra were tested, and the results are shown in Figure Figure 6 shows the surface roughness of the modified silicone coatings. It was found that with the addition of PDMS2200, the surface roughness of the coatings was greatly reduced. This is because the addition of silicone segments increased the degree of microphase separation of the polyurethane. Compared with the interior of the coating, silicone tended to enrich on the surface. A large amount of silicone formed a continuous phase on the coating's surface, thereby improving its flatness. With continued increases in X PDMS , the continuous phase did not change much, so its roughness was maintained in a relatively stable state. The chemical shift near 0 ppm corresponded to the proton on the Si-CH3 gro chemical shift at δ = 0.79-1.48 ppm was attributed to hydrogen on methylene linked to Si in PDMS2200. The chemical shift around 1.7 ppm corresponded to the group on TDI. The chemical shift at δ = 2.0-2.5 ppm was attributed to methyl an ylene groups on PED and PET. The chemical shift at δ = 3.5 ppm corresponded to gen on methyne linked to carbamate; the multiple signal peaks near 4.0 ppm tributed to the protons in methylene on PDMS2200. Combined with ATR-FTIR sp could be determined that polyurethane-modified silicone coatings were successfu pared. Figure 6 shows the surface roughness of the modified silicone coatings. It wa that with the addition of PDMS2200, the surface roughness of the coatings was reduced. This is because the addition of silicone segments increased the degre crophase separation of the polyurethane. Compared with the interior of the coat cone tended to enrich on the surface. A large amount of silicone formed a con phase on the coating's surface, thereby improving its flatness. With continued i in XPDMS, the continuous phase did not change much, so its roughness was maint a relatively stable state. The microphase separation on the surface of the PU-Si17 coating was obse AFM, and the results are shown in Figure 7. It was found that apparent phase se occurred on the surface of the modified coating. The part with a darker color and The microphase separation on the surface of the PU-Si17 coating was observed by AFM, and the results are shown in Figure 7. It was found that apparent phase separation occurred on the surface of the modified coating. The part with a darker color and concave surface corresponds to the soft segment in the coating, and the part with a brighter color and convex surface is the hard segment area. It was seen that the continuous phase on the surface of the coating was composed of soft segments dominated by silicone, and a small number of hard segments was dispersed in the soft segments. This result proves the above inference.

Contact Angle and Surface Free Energy
The contact angles of the modified coatings are shown in Figure 8. All the water tact angles were greater than 107°, indicating that all the modified coatings had good drophobicity. Because the addition of PDMS2200 made more silicone enrich on the ings' surfaces, improving the hydrophobicity, the water contact angle increased; th crease of the contact angle may have been caused by the change of its surface roughn The surface-free energy of the modified coatings was calculated, and the result shown in Figure 9. It was found that with the increase of PDMS2200, the surface en of the coatings increased continuously. On the one hand, according to the Cassie m [32,33], the higher the roughness of the coating surface, the more difficult it is for the li to wet the surface, and the lower the surface energy; on the other hand, according t calculation formula of the surface energy [32], it was seen that the surface energy o coating was composed of the polar force and the dispersion force. Comparing these

Contact Angle and Surface Free Energy
The contact angles of the modified coatings are shown in Figure 8. All the water contact angles were greater than 107 • , indicating that all the modified coatings had good hydrophobicity. Because the addition of PDMS2200 made more silicone enrich on the coatings' surfaces, improving the hydrophobicity, the water contact angle increased; the decrease of the contact angle may have been caused by the change of its surface roughness.

Contact Angle and Surface Free Energy
The contact angles of the modified coatings are shown in Figure 8. All the water c tact angles were greater than 107°, indicating that all the modified coatings had good drophobicity. Because the addition of PDMS2200 made more silicone enrich on the co ings' surfaces, improving the hydrophobicity, the water contact angle increased; the crease of the contact angle may have been caused by the change of its surface roughne The surface-free energy of the modified coatings was calculated, and the results shown in Figure 9. It was found that with the increase of PDMS2200, the surface ene of the coatings increased continuously. On the one hand, according to the Cassie mo The surface-free energy of the modified coatings was calculated, and the results are shown in Figure 9. It was found that with the increase of PDMS2200, the surface energy of the coatings increased continuously. On the one hand, according to the Cassie model [32,33], the higher the roughness of the coating surface, the more difficult it is for the liquid to wet the surface, and the lower the surface energy; on the other hand, according to the calculation formula of the surface energy [32], it was seen that the surface energy of the coating was composed of the polar force and the dispersion force. Comparing these two forces, it was found that the polar force could be ignored, and the dispersion force was mainly related to the degree of molecular deformation-the greater the degree, the stronger the dispersion force. As shown in Figure 9, with the continuous addition of PDMS2200, a large number of Si and O atoms significantly improved the flexibility of the molecular chain of the modified coatings, thereby increasing the dispersion force of the coating to a certain extent. Furthermore, the surface energy of the coatings continued to increase. lymers 2022, 14, x FOR PEER REVIEW PDMS2200, a large number of Si and O atoms significantly improved the molecular chain of the modified coatings, thereby increasing the dispe coating to a certain extent. Furthermore, the surface energy of the coati increase.
Under the combined effect of roughness and dispersion force, the su of the modified coatings showed a rising trend with the increase of XPDM

Tensile Properties
Tensile tests were carried out on the modified silicone coatings, and ulus was calculated. As shown in Figure 10, the introduction of PDMS modified coatings' elastic moduli. This is because PDMS2200 increased soft segment and improved the flexibility of the molecular chain, so the the coatings decreased; with the continuous improvement of XPDMS, the fect of the hard segment on the coatings was reflected, thereby improving uli of the coatings. Under the combined effect of roughness and dispersion force, the surface free energy of the modified coatings showed a rising trend with the increase of X PDMS .

Tensile Properties
Tensile tests were carried out on the modified silicone coatings, and their elastic modulus was calculated. As shown in Figure 10, the introduction of PDMS2200 reduced the modified coatings' elastic moduli. This is because PDMS2200 increased the length of the soft segment and improved the flexibility of the molecular chain, so the elastic moduli of the coatings decreased; with the continuous improvement of X PDMS , the strengthening effect of the hard segment on the coatings was reflected, thereby improving the elastic moduli of the coatings.
The elongation and breaking strength of the modified coatings are shown in Figures 11 and 12, respectively. It was found that with the increase of X PDMS , the elongation and breaking strength of the coatings both showed a trend of increasing first and then decreasing. This is because the addition of PDMS2200 improved the flexibility of the molecular chain, so its elongation was enhanced. At the same time, the hard segment generated by the microphase separation of the polyurethane acted as the second phase to strengthen the mechanical properties of the coating, thereby improving the breaking strength of the modified coatings; as X PDMS continued to increase, the size of the hard segment was also growing, which made the deformation of the molecular chain more difficult, resulting in a decrease in the elongation of the coating. The increasing microphase separation led to an increase in the interface between soft and hard segments. These interfaces were more prone to stress concentration when subjected to external forces, which led to crack nucleation, so the fracture strength of the coating decreased. Figure 9. Surface-free energy and dispersion force of modified silicone coatings.

Tensile Properties
Tensile tests were carried out on the modified silicone coatings, and their e ulus was calculated. As shown in Figure 10, the introduction of PDMS2200 modified coatings' elastic moduli. This is because PDMS2200 increased the le soft segment and improved the flexibility of the molecular chain, so the elasti the coatings decreased; with the continuous improvement of XPDMS, the streng fect of the hard segment on the coatings was reflected, thereby improving the e uli of the coatings. The elongation and breaking strength of the modified coatings are show 11 and 12, respectively. It was found that with the increase of XPDMS, the elon breaking strength of the coatings both showed a trend of increasing firs decreasing. This is because the addition of PDMS2200 improved the flexibility lecular chain, so its elongation was enhanced. At the same time, the hard segm ated by the microphase separation of the polyurethane acted as the secon strengthen the mechanical properties of the coating, thereby improving th strength of the modified coatings; as XPDMS continued to increase, the size of th ment was also growing, which made the deformation of the molecular chain cult, resulting in a decrease in the elongation of the coating. The increasing separation led to an increase in the interface between soft and hard segments. faces were more prone to stress concentration when subjected to external fo led to crack nucleation, so the fracture strength of the coating decreased.

Antifouling Performance
The bacterial and benthic diatom adhesion experiments were carried out on the ified coatings, and their colony area rate and chlorophyll concentration are shown ures 13 and 14, respectively. It was found that with the continuous addition of PDM the colony area rate and chlorophyll concentration on the coatings' surfaces sho

Antifouling Performance
The bacterial and benthic diatom adhesion experiments were carried out on the modified coatings, and their colony area rate and chlorophyll concentration are shown in Figures 13 and 14, respectively. It was found that with the continuous addition of PDMS2200, the colony area rate and chlorophyll concentration on the coatings' surfaces showed a trend of first decreasing and then increasing. Furthermore, the washing treatment could effectively remove the bacteria and benthic diatoms attached to the coatings' surfaces.
Polymers 2022, 14, x FOR PEER REVIEW trend of first decreasing and then increasing. Furthermore, the washing treatmen effectively remove the bacteria and benthic diatoms attached to the coatings' surfa

Discussion
Brady [34] once proposed the relative adhesion factor (RAF), which is consid essential basis for characterizing the antifouling performance of silicone coatings. calculated with the following equation: where E denotes the elastic modulus of the coating, and γ denotes the surface free of the coating. The results of the RAF are shown in Figure 15. It was found that rinsed samples, the colony area rate was entirely in line with Brady's theory, tha smaller the RAF, the better the antifouling performance of the coating; for the w sample, the change of the colony area rate and RAF was not precisely the same may have been caused by the roughness Ra of the coating surface.

Discussion
Brady [34] once proposed the relative adhesion factor (RAF), which is considered an essential basis for characterizing the antifouling performance of silicone coatings. RAF is calculated with the following equation: where E denotes the elastic modulus of the coating, and γ denotes the surface free energy of the coating. The results of the RAF are shown in Figure 15. It was found that for the rinsed samples, the colony area rate was entirely in line with Brady's theory, that is, the smaller the RAF, the better the antifouling performance of the coating; for the washed sample, the change of the colony area rate and RAF was not precisely the same, which may have been caused by the roughness Ra of the coating surface.
Polymers 2022, 14, x FOR PEER REVIEW Figure 15. Relationship between the RAF and the colony area rate of the modified silicone Therefore, based on RAF, the roughness of the coating surface was introduc a new relative adhesion factor RAF' was proposed; it was calculated with the fo equation: Figure 15. Relationship between the RAF and the colony area rate of the modified silicone coatings. Therefore, based on RAF, the roughness of the coating surface was introduced, and a new relative adhesion factor RAF was proposed; it was calculated with the following equation: The results of RAF' and the colony area rate of the washed samples are shown in Figure 16. It was found that the smaller the RAF', the lower the colony area rate. This indicates that the removal of fouling organisms on the surface of the modified silicone coating prepared in this paper was controlled by its elastic modulus, surface energy, and roughness. Figure 15. Relationship between the RAF and the colony area rate of the modified silicone coat Therefore, based on RAF, the roughness of the coating surface was introduced, a new relative adhesion factor RAF' was proposed; it was calculated with the follow equation: The results of RAF' and the colony area rate of the washed samples are show Figure 16. It was found that the smaller the RAF', the lower the colony area rate. indicates that the removal of fouling organisms on the surface of the modified sili coating prepared in this paper was controlled by its elastic modulus, surface energy, roughness. Based on the above, it can be seen that the increase of XPDMS will aggravate the crophase separation of the modified coatings, thereby reducing the roughness of the c ing surface, which will improve the wetting and dispersibility of the liquid on the coa surface to a certain extent. The introduction of PDMS2200 brings a large number of S well as O atoms, which will improve the dispersion force of the modified coatings. U the combined action of these two factors, the coating γ will continue to increase with increase of XPDMS.
At the same time, the introduction of PDMS2200 will also increase the content o soft segment, which will improve the deformation ability of the modified coat Based on the above, it can be seen that the increase of X PDMS will aggravate the microphase separation of the modified coatings, thereby reducing the roughness of the coating surface, which will improve the wetting and dispersibility of the liquid on the coating surface to a certain extent. The introduction of PDMS2200 brings a large number of Si, as well as O atoms, which will improve the dispersion force of the modified coatings. Under the combined action of these two factors, the coating γ will continue to increase with the increase of X PDMS .
At the same time, the introduction of PDMS2200 will also increase the content of the soft segment, which will improve the deformation ability of the modified coatings, thereby reducing its E; when the content of PDMS2200 exceeds a certain level, the strengthening effect of the hard segment is reflected, and continuing to increase X PDMS will lead to an increase in E instead of a decrease. Therefore, by controlling X PDMS , the modified coatings can obtain a more suitable degree of microphase separation to obtain lower E, γ, and Ra, giving the modified coatings good antifouling performance.

Conclusions
In this paper, PED-TDI polyurethane-modified silicone coatings were prepared, and the effects of soft segments on the structure and properties of modified coatings were investigated by introducing different contents of PDMS2200 into polyurethane.
(1) By analyzing the infrared spectrum and NMR spectrum of PED-TDI polyurethane and its modified coatings, it was found that isocyanate-terminated polyurethane was successfully prepared, and it was successfully used to modify silicone; (2) When X PDMS = 23 mol%, the modified coating has the lowest surface roughness, which is 0.0565 µm; when X PDMS = 0 mol%, the surface free energy of the modified coatings is the lowest, which is 26.01 mJ/m 2 ; when X PDMS = 11 mol%, the elastic modulus of the modified coatings is the lowest, which is 1.30 MPa; (3) The antifouling effect of the modified silicone coatings is related to its own RAF . Polyurethane with different soft segment compositions changes the coating's elastic modulus, surface energy, and roughness by affecting the microphase separation degree, which finally influences the antifouling properties. When X PDMS = 17 mol%, the modified coatings can obtain better mechanical properties and antifouling effects.