Fungal Biodegradation of Polyurethanes

Polyurethanes (PURs) are versatile polymers used in a wide variety of fields, such as the medical, automotive, textile, thermal insulation, and coating industries as well as many everyday objects. Many PURs have applications that require a long service life, sometimes with exposure to aggressive conditions. They can undergo different types of physicochemical and biological degradation, but they are not compostable, and many of them constitute persistent waste in the environment. Although both bacteria and fungi can be involved in the degradation of PURs, fungi are often the main biodegradation agents. The chemical structure of PURs determines their degree of biodegradation. Fungal biodegradation of PURs is linked to the production of enzymes, mainly esterases and proteases, alongside laccases, peroxidases, and tyrosinases, which can modify the structure of polyurethane compounds by forming carbonyl groups. The experimental analysis of the biodegradation of PUR can be carried out by bringing the polymer into contact with a mold in pure culture or with a microbial consortium. Then, global measurements can be taken, such as weight loss, tensile tests, or the ability of microorganisms to grow in the presence of PUR as the sole carbon source. The analysis of the chemical structure of the polymer and its degradation products after fungal growth can confirm biodegradation and specify the mechanism. The main avenues of future research are directed towards the development of fully biodegradable PURs and, on the contrary, towards the development of PURs that are more resistant to degradation phenomena, in particular biodegradation, for applications where the material is in contact with living organisms.


Introduction
Since their development in the 1930s, polyurethanes (PURs) have played an important role in a large variety of applications [1]. They are used in medical, automotive, textile, thermal insulative, coating, and everyday objects. PURs can be found in car seats, furniture, mattresses, clothing, waterproof coatings, paints, and pipes. This presence in many fields of application is linked to the versatility of polymers with urethane functions. However, polyurethanes usually have other functions (urea, ether, ester, aromatic, hydroxide, amine, etc.) and, thus, present a wide variety of physical or chemical properties.
Generally, urethane bonds -O-(C=O)-NH-are obtained by reactions between alcohols -OH and isocyanates -N=C=O. Polyurethane is a polymer containing several urethane bonds in its chain. To form a PUR, polyols, and diisocyanates are used. PURs are composed of a succession of hard and soft segments, themselves composed, respectively, of isocyanates and polyols. The nature of the polyol and the isocyanate determines the final properties of the polymer, such as its softness, hardness, and flexibility. Thus, the flexibility of PUR is increased by lengthening the chain of the polyol. Isocyanates are molecules with short chains that constitute areas of increased crystallization, hence the name "hard tyrosinases are thought to modify the structure of polyurethane compounds by forming carbonyl groups [33,34]. The fungal biodegradation process is increased when C=C double bonds are present in PUR [35].
The chemical structure of PURs determines their biodegradation under composting conditions [36]. As in other conditions of exposure to microbial attack, a PEUR is less susceptible to biodegradation than a PESTUR during composting. The increase in the number of hard segments or the presence of aromatic diisocyanates decreases the biodegradability of PUR, unlike that of aliphatic diisocyanates [5,36]. The biodegradation of PESTUR by thermophilic and thermotolerant fungi is observed at an increased rate during the thermophilic and early maturation phases of the composting process. Thus, the Thermomyces lanuginosus species, which produces numerous enzymes (thermostable proteases, amylases, xylanases, ureases, and lipases), are dominant on the surface of PESTUR coupons at 50 and 55 • C [5].
Bio-based PESTUR and, in particular, vegetable oil-based PESTUR can be engineered to be fully biodegradable [37][38][39]. Such polymers can be rapidly biodegraded in compost, soil, and natural ocean environments by depolymerization, resulting in the release of original monomers that are then consumed during microbial growth. In the study by Gunawan et al., SEM imaging showed progressive degradation over time of biodegradable PUR samples during immersion in the ocean (Figure 1) [39]. This biodegradation resulted in increased porosity, crumbling, and cracking of the foam surface ( Figure 1B-D) compared to the surface of a foam sample not submerged in the ocean ( Figure 1A). Biodegradation of Starch-PUR films in soil occurs in successive steps as follows: wetting and colonization by microorganisms, hydrolysis of the starch part, fractionation of the polymer into small structures, and slow degradation of the polyurethane part [40].
Biodegradable PURs with anti-fouling properties have been described [41,42]. Marine biofouling is a major challenge for various human activities, including the performance and longevity of boat hulls. One of the most common approaches to combating marine biofouling is to develop anti-fouling coatings. Ma et al. have developed a biodegradable PUR whose soft segments are composed of dihydroxyl-terminated copolyester oligomers made of ε-caprolactone and glycolide [41]. The ester bond is the most sensitive zone to microbial attack, which allows the biodegradation of the material. The PUR material is designed to be eroded in the seawater environment, leading to a self-renewing and antifouling surface. Inorganic, organic, and living foulants attached to the coating detach from the surface during its degradation. The anti-biofouling activity of the degradable PUR depends on its rate of degradation; it increases with the rate of degradation for a glycolide content of 0 to 10% in moles. Anti-fouling efficiency and coating durability can be improved by adding the commonly used biocide 4,5-Dichloro-2-octylisothiazolone (DCOIT). Ali et al. have synthesised a biodegradable composite material corresponding to a polyurethane composed of ε-caprolactone, 4,4 -methylene bis(cyclohexyl isocyanate), and 1,4 butanediol, incorporating DCOIT and clay [42]. The adhesion strength and rate of degradation of the material are increased following the addition of clay by reducing the spherulite size and crystallinity of the polycaprolactone (PCL), which improves the amorphous interfacial region of the composite material. DCOIT molecules localized in the amorphous region give the material anti-adhesion properties against microorganisms. By reducing the size of the PCL, spherulite in the composite, the clay facilitates the enzymatic attack of the material. Biodegradable PURs with anti-fouling properties have been described [41,42]. Marine biofouling is a major challenge for various human activities, including the performance and longevity of boat hulls. One of the most common approaches to combating marine biofouling is to develop anti-fouling coatings. Ma et al. have developed a biodegradable PUR whose soft segments are composed of dihydroxyl-terminated copolyester oligomers made of ε-caprolactone and glycolide [41]. The ester bond is the most sensitive zone to microbial attack, which allows the biodegradation of the material. The PUR material is designed to be eroded in the seawater environment, leading to a self-renewing and anti-fouling surface. Inorganic, organic, and living foulants attached to the coating detach from the surface during its degradation. The anti-biofouling activity of the degradable PUR depends on its rate of degradation; it increases with the rate of degradation for a glycolide content of 0 to 10% in moles. Anti-fouling efficiency and coating durability can be improved by adding the commonly used biocide 4,5-Dichloro-2-octylisothiazolone (DCOIT). Ali et al. have synthesised a biodegradable composite material corresponding to a polyurethane composed of ε-caprolactone, 4,4′-methylene bis(cyclohexyl isocyanate), and 1,4 butanediol, incorporating DCOIT and clay [42]. The adhesion strength and rate of degradation of the material are increased following the addition of clay by reducing the spherulite size and crystallinity of the polycaprolactone (PCL), which improves the amorphous interfacial region of the composite material. DCOIT molecules localized in the amorphous region give the material anti-adhesion properties against microorganisms. By reducing the size of the PCL, spherulite in the composite, the clay facilitates the enzymatic attack of the material.
Conventional PURs with anti-adhesion properties among microorganisms can be obtained by modifying the surface of the material [43,44]. Weintraub et al. coated the surface of a polyurethane catheter with a copolymer of astaxanthin (ATX) and polyethylene glycols (PEG) to develop an implantable medical device resistant to infections [43]. ATX is a xanthophyll carotenoid with antimicrobial properties. ATX can be polymerized with dif- Conventional PURs with anti-adhesion properties among microorganisms can be obtained by modifying the surface of the material [43,44]. Weintraub et al. coated the surface of a polyurethane catheter with a copolymer of astaxanthin (ATX) and polyethylene glycols (PEG) to develop an implantable medical device resistant to infections [43]. ATX is a xanthophyll carotenoid with antimicrobial properties. ATX can be polymerized with different dicarboxylic acid co-monomers. The biodegradation of the polymer coating in vivo and the antimicrobial properties of the material depend on the size of the PEG block. p(ATX-co-PEG 2000) is rapidly biodegraded and has no satisfactory antimicrobial properties in vivo. p(ATX-co-PEG 1000) and p(ATX-co-PEG 250) have antimicrobial properties in vivo that are negatively correlated with their rate of biodegradation. The slower the biodegradation rate, the more gradual the release of ATX and the better the antimicrobial properties. De La Franier et al. used another strategy to develop a PUR that reduces the adhesion of microorganisms to the surface of indwelling urinary catheters [44]. The anti-fouling material was a monolayer of monoethylene glycol hydroxide (MEG-OH) covalently bound to PUR via a siloxane network. After in vitro exposure for 24 to 72 h at 37 • C, a decrease in adherent bacteria varying from 85 to 96% was observed depending on the species tested, and a decrease of 90% was observed for Candida albicans. Moreover, only scattered microorganisms and small clusters of a few adherent cells formed on the MEG-OH coating without the development of biofilm, contrary to the strong formation of biofilm on the control PUR. A similar level of anti-adhesion was maintained after autoclaving or storing the material in the air for 4.5 months. The mechanism of the microbial anti-adhesion effect is unknown, but the anti-fouling activity of MEG-OH for blood and proteins is associated with the formation of an interfacial layer of hydration due to ether groups in the middle of chain [45].

Experimental Analysis of Polyurethane Biodegradation
The weight loss measurement is a global analysis, which constitutes the first global approach for studying the biodegradation of PURs [46,47]. This technique is not highly sensitive and requires significant biodegradation of the polymer to be efficient. In the study by Magnin et al., thermoplastic polyurethanes had a mass loss of a few percent (9% maximum) after exposure for two months at 30 • C to strains of Alternaria, Penicillium, or Aspergillus ( Figure 2) [46]. In order not to underestimate biodegradation, it is essential to rid the material of all the biomass that has developed on its surface. For this, washes with mechanical action and chemical treatments with ethanol, a non-ionic surfactant, or sodium hypochlorite can be used [27,28,47].
37 °C, a decrease in adherent bacteria varying from 85 to 96% was observed depending on the species tested, and a decrease of 90% was observed for Candida albicans. Moreover, only scattered microorganisms and small clusters of a few adherent cells formed on the MEG-OH coating without the development of biofilm, contrary to the strong formation of biofilm on the control PUR. A similar level of anti-adhesion was maintained after autoclaving or storing the material in the air for 4.5 months. The mechanism of the microbial anti-adhesion effect is unknown, but the anti-fouling activity of MEG-OH for blood and proteins is associated with the formation of an interfacial layer of hydration due to ether groups in the middle of chain [45].

Experimental Analysis of Polyurethane Biodegradation
The weight loss measurement is a global analysis, which constitutes the first global approach for studying the biodegradation of PURs [46,47]. This technique is not highly sensitive and requires significant biodegradation of the polymer to be efficient. In the study by Magnin et al., thermoplastic polyurethanes had a mass loss of a few percent (9% maximum) after exposure for two months at 30 °C to strains of Alternaria, Penicillium, or Aspergillus ( Figure 2) [46]. In order not to underestimate biodegradation, it is essential to rid the material of all the biomass that has developed on its surface. For this, washes with mechanical action and chemical treatments with ethanol, a non-ionic surfactant, or sodium hypochlorite can be used [27,28,47]. To identify microorganisms that biodegrade PURs, colloidal model polymers like Impranil-DLN ® can be used. Impranil-DLN ® is an ester-urethane that is easily degradable and assimilated by microorganisms. It can induce the fungal secretion of PUR-degrading enzymes active against both PESTUR and PEUR. Impranil-DLN ® forms a whitish, opaque surface when dispersed in an agar-supercooled medium [23,26,48]. Its biodegradation To identify microorganisms that biodegrade PURs, colloidal model polymers like Impranil-DLN ® can be used. Impranil-DLN ® is an ester-urethane that is easily degradable and assimilated by microorganisms. It can induce the fungal secretion of PUR-degrading enzymes active against both PESTUR and PEUR. Impranil-DLN ® forms a whitish, opaque surface when dispersed in an agar-supercooled medium [23,26,48]. Its biodegradation leads to the appearance of translucent zones around the microbial colonies. A biodegradation test can also be carried out in a liquid medium. The turbidity measurement correlated to the concentration of impranil-DLN ® makes it possible to assess its degradation after 14 days of incubation in the presence of mold [28]. These tests based on the disappearance of colloidal-polymer-related opaque cloudiness can reveal the degradation of a PUR by enzymatic hydrolysis of urethane bonds but also of ester bonds [49].
In the study by Darby and Kaplan (1968), about 100 PURs of different chemical compositions were subjected to a mixture of molds containing several species of Aspergillus, Penicillium, Trichoderma, and Chaetomium globosum (Table 1) [21]. The polyurethanes were synthesized from various dialcohols or polyesters such as 1,5-Pentanediol, 3-Methyl-2,4-pentanediol, 2-Methyl-2,4-pentanediol, Diethylene glycol, Dipropylene glycol, Polypropylene glycol, Polyethylene glycol adipate, Poly-1,3-propanediol adipate, and various diisocyanates, including tolylene-2,4-diisocyanate, diphenylmethane-4,4 -diisocyanate, 3,3bitolylene-4,4 -diisocyanate, and 1,6-hexamethylene-diisocyanate. These polymers were then placed on agar plates for individual testing. The mold mixture was inoculated, and growth was observed after 2-3 weeks at 30 • C. The growth rate was assessed visually. The mold growth rate defines the ability to use the polymer as a nutrient source. A high growth rate, therefore, corresponds to the high biodegradation of the polymer. PESTURs were shown to be more easily degraded by molds than PEURs, and biodegradation occurred more favorably in the presence of a sufficiently long carbon chain between the urethane bonds. The greater sensitivity of PESTURs to biodegradation has been confirmed by other studies [9,10,[22][23][24][25][26][27][28]. In the study by Plancher et al., a translucent ground PEUR was incorporated into supercooled agar or supercooled agar containing low-concentration malt extract [31]. Comparative growth of molds on these different media showed the ability of a Penicillium sp. strain to metabolize PEUR as a sole nutrient source or in the presence of other nutrients at low concentrations ( Figure 3). Thus, the diameter of Penicillium colonies exceeded 2 cm in diameter after 350 h at 24 • C in the presence of malt extract and PEUR, whereas it was less than 0.5 cm in the presence of malt extract or PEUR alone. In the same conditions, Aspergillus niger only grew in the presence of malt extract; its growth rate was not modified by the presence of PEUR.
After its biodegradation, an analysis of the chemical composition of the polymer and the appearance of its degradation products can be performed. After 14 days of growth of Cladosporium pseudocladosporioides strain T1.PL.1 in a minimal medium containing Impranil-DLN ® , FTIR analysis of cell-free filtrates revealed a decrease in signals corresponding to the carbonyl group (C=O) and the urethane bond (C-N-H) [28]. The analysis of the compounds present in the incubation medium was carried out by GC-MS in the presence and absence of mold. In the absence of mold, minor changes in some compounds were observed. On the other hand, significant changes in the profile of the compounds were observed after fungal growth, with some disappearing and others appearing. This confirmed a decrease in compounds with the ester bond and an increase in alcohols and hexane diisocyanate, which highlighted the biodegradation of Impranil-DLN ® . Detection of aromatic amines released during fungal biodegradation of Tolyl-carbamate urethane compounds can also be performed by GC-MS to confirm the cleavage of urethane groups [32]. In addition to revealing the biodegradation of a PUR, FTIR analysis can also help identify the mechanism. Significant decreases in band intensities at 890 (C-C stretch), 960 (C-C stretch), Penicillium on an agar medium containing the PEUR PUX1520 [31]. The same experiment carried out with a strain of Aspergillus niger showed few changes in the IR spectrum of PEUR except for an increase in the signal at 1710 cm −1 . Each of these two strains proved capable of biodegrading PEUR PUX1520 after 4 weeks of incubation at 24 • C in a broth containing the polymer and malt extract. A closer analysis of the carbonyl group and full-spectrum IR signals revealed oxidative degradation of the polymer [31]. It has long been known that photooxidation is a major factor in the degradation of polyether-based polyurethanes [50]. Oxidation is also a major factor in the microbial biodegradation of polyether urethanes [31,[51][52][53].  After its biodegradation, an analysis of the chemical composition of the polymer and the appearance of its degradation products can be performed. After 14 days of growth of Cladosporium pseudocladosporioides strain T1.PL.1 in a minimal medium containing Impranil-DLN ® , FTIR analysis of cell-free filtrates revealed a decrease in signals corresponding to the carbonyl group (C=O) and the urethane bond (C-N-H) [28]. The analysis of the compounds present in the incubation medium was carried out by GC-MS in the presence and absence of mold. In the absence of mold, minor changes in some compounds were observed. On the other hand, significant changes in the profile of the compounds were observed after fungal growth, with some disappearing and others appearing. This confirmed a decrease in compounds with the ester bond and an increase in alcohols and hex- The ISO 846 standard for the determination of the deterioration of plastics when exposed to microorganisms is well suited to the study of the biodegradation of PURs [18]. In this standard, indirect or direct deterioration caused by microorganisms is determined by visual observation, measurement of mass changes, and measurement of changes in other physical properties like surface gloss, bending properties, impact resistance, and hardness. It is only applicable to materials with a flat surface. It includes five main methods for determining the resistance of plastics to fungi (method A), fungistatic effects (methods B and B ), resistance to bacteria (method C), and resistance to soil microorganisms (method D). Figure 4 shows a fungal growth test on a PEUR according to ISO 846, methods B and A. Strong growth of Aspergillus niger was observed on the polymer in different conditions. The higher spore density at the edges of the polymer than elsewhere on the agar medium was observed macroscopically ( Figure 4B). The presence of mycelial filaments running along the surface of the polymer and spores reaching the center of the polymer were observed under light and scanning electron microscopy ( Figure 4B,C).
The ISO 846 standard for the determination of the deterioration of plastics when exposed to microorganisms is well suited to the study of the biodegradation of PURs [18]. In this standard, indirect or direct deterioration caused by microorganisms is determined by visual observation, measurement of mass changes, and measurement of changes in other physical properties like surface gloss, bending properties, impact resistance, and hardness. It is only applicable to materials with a flat surface. It includes five main methods for determining the resistance of plastics to fungi (method A), fungistatic effects (methods B and B′), resistance to bacteria (method C), and resistance to soil microorganisms (method D). Figure 4 shows a fungal growth test on a PEUR according to ISO 846, methods B′ and A. Strong growth of Aspergillus niger was observed on the polymer in different conditions. The higher spore density at the edges of the polymer than elsewhere on the agar medium was observed macroscopically ( Figure 4B). The presence of mycelial filaments running along the surface of the polymer and spores reaching the center of the polymer were observed under light and scanning electron microscopy ( Figure 4B,C). Among the physical property changes associated with biodegradation, the mechanical strength of materials in tensile tests can be measured [54,55]. Exposure of polyurethane elastomer films to a strain of Chaetomium globosum for 90 days at 28 • C induces a decrease in breaking stress and tensile strength [52]. Figure 5 shows the comparison of the behavior of a PUR material with or without exposure to the growth of A. niger, according to ISO 846, method B , in a tensile test according to the ISO 527-2 standard [56]. After exposure to A. niger, an increase in the maximum stress of 6.9 to 8.8 N/mm 2 and a decrease in strain of 37 to 16% before failure were observed ( Figure 5).
One of the difficulties of protocols for studying PUR biodegradation during fungal growth in vitro is the sterilization of the material before exposure. Although it does not induce mass loss and can be used for foams, autoclaving can induce alterations in many PURs [28,57]. UV irradiation can be used, but this can also degrade the chemical structure and mechanical properties of PUR [4,58]. Thus, UV irradiation can induce breaks in the polymer chain at the molecular level and yellowing, cracks, and holes at the macroscopic scale. Figure 6 shows the macroscopically visible yellowing of PUR after autoclaving or UV-C irradiation. Colorimetric analysis of the coupons indicated E values of 84.61, 83.53, and 80.53 for the control, autoclaved, and UV-C irradiated samples, respectively. The color difference ∆E*ab between the control and the UV-C-treated PUR was 4.9.
the same material incubated under the same conditions in the presence of A. niger (right picture).
Among the physical property changes associated with biodegradation, the mechanical strength of materials in tensile tests can be measured [54,55]. Exposure of polyurethane elastomer films to a strain of Chaetomium globosum for 90 days at 28 °C induces a decrease in breaking stress and tensile strength [52]. Figure 5 shows the comparison of the behavior of a PUR material with or without exposure to the growth of A. niger, according to ISO 846, method B′, in a tensile test according to the ISO 527-2 standard [56]. After exposure to A. niger, an increase in the maximum stress of 6.9 to 8.8 N/mm 2 and a decrease in strain of 37 to 16% before failure were observed ( Figure 5).

Figure 5.
Evolution of the strain of a PUR material as a function of the stress applied in a tensile test. Comparison of an unexposed material (control) with a material exposed to the growth of Aspergillus niger according to method B′ of the ISO 846 standard.
One of the difficulties of protocols for studying PUR biodegradation during fungal growth in vitro is the sterilization of the material before exposure. Although it does not induce mass loss and can be used for foams, autoclaving can induce alterations in many PURs [28,57]. UV irradiation can be used, but this can also degrade the chemical structure and mechanical properties of PUR [4,58]. Thus, UV irradiation can induce breaks in the polymer chain at the molecular level and yellowing, cracks, and holes at the macroscopic scale. Figure 6 shows the macroscopically visible yellowing of PUR after autoclaving or UV-C irradiation. Colorimetric analysis of the coupons indicated E values of 84.61, 83.53, and 80.53 for the control, autoclaved, and UV-C irradiated samples, respectively. The color difference ΔE*ab between the control and the UV-C-treated PUR was 4.9. An ethanol rinse has been used in some studies to sterilize PUR coupons before exposure [24,27]. The Standard ISO 846 recommends cleaning polyurethane coupons in a 30% ethanol bath and, in some cases, disinfecting coupons in an o-phenylphenol bath at a concentration of 1 g/L [18]. A solution of o-phenylphenol 0.1% (weight/volume) and 79% ethanol (volume/volume) in water was effective against a mixture of Staphylococcus aureus, Mycobacterium bovis, spores of Trichophyton mentagrophytes, and Sabin poliovirus type 1 but not against spores of Bacillus stearothermophilus [59]. By using the cleaning/disinfection protocol recommended by standard ISO 846, the persistence of bacterial and fungal contaminants on PUR coupons is frequently observed (Figure 7). In the example shown in Figure 7, there was no growth of contaminants from PUR coupon numbers 1, 2, 4, and 6, while bacterial growth and fungal growth were observed from coupon numbers 3 and 5, respectively. However, the six coupons underwent the same cleaning and disinfection protocol. An ethanol rinse has been used in some studies to sterilize PUR coupons before exposure [24,27]. The Standard ISO 846 recommends cleaning polyurethane coupons in a 30% ethanol bath and, in some cases, disinfecting coupons in an o-phenylphenol bath at a concentration of 1 g/L [18]. A solution of o-phenylphenol 0.1% (weight/volume) and 79% ethanol (volume/volume) in water was effective against a mixture of Staphylococcus aureus, Mycobacterium bovis, spores of Trichophyton mentagrophytes, and Sabin poliovirus type 1 but not against spores of Bacillus stearothermophilus [59]. By using the cleaning/disinfection protocol recommended by standard ISO 846, the persistence of bacterial and fungal contaminants on PUR coupons is frequently observed (Figure 7). In the example shown in Figure 7, there was no growth of contaminants from PUR coupon numbers 1, 2, 4, and 6, while bacterial growth and fungal growth were observed from coupon numbers 3 and 5, respectively. However, the six coupons underwent the same cleaning and disinfection protocol.
but not against spores of Bacillus stearothermophilus [59]. By using the cleaning/disinfection protocol recommended by standard ISO 846, the persistence of bacterial and fungal contaminants on PUR coupons is frequently observed (Figure 7). In the example shown in Figure 7, there was no growth of contaminants from PUR coupon numbers 1, 2, 4, and 6, while bacterial growth and fungal growth were observed from coupon numbers 3 and 5, respectively. However, the six coupons underwent the same cleaning and disinfection protocol.

Figure 7.
Observation of the growth of contaminants (red arrows, Petri dishes 3 and 5) developing from PUR coupons deposited on nutrient agar (Petri dish 9 cm in diameter) after cleaning with ethanol and disinfection with o-phenylphenol after 6 weeks of incubation at 27 °C/80% relative humidity according to ISO 846.
Adaptations of the protocols recommended by the ISO 846 standard make it possible to improve the decontamination efficiency of the surface of PUR coupons. Figure 8 shows the result obtained after the application of a disinfection protocol composed of a sterile distilled water bath, followed by an ethanol bath at its bactericidal concentration of 70% [60], and a bath of o-phenylphenol at an increased concentration of 1% (weight/volume) Adaptations of the protocols recommended by the ISO 846 standard make it possible to improve the decontamination efficiency of the surface of PUR coupons. Figure 8 shows the result obtained after the application of a disinfection protocol composed of a sterile distilled water bath, followed by an ethanol bath at its bactericidal concentration of 70% [60], and a bath of o-phenylphenol at an increased concentration of 1% (weight/volume) effective against microorganisms in vegetative and spore form [61]. Incubation on agar was carried out in the presence of a 1% o-phenylphenol solution on the PUR coupons. After the application of this protocol to PUR coupons and 6 weeks of incubation, the absence of contaminants was demonstrated (Figure 8). This is an important point of the ISO 846 standard, which requires testing a batch of incubated material without inoculation by microorganisms. effective against microorganisms in vegetative and spore form [61]. Incubation on agar was carried out in the presence of a 1% o-phenylphenol solution on the PUR coupons.
After the application of this protocol to PUR coupons and 6 weeks of incubation, the absence of contaminants was demonstrated ( Figure 8). This is an important point of the ISO 846 standard, which requires testing a batch of incubated material without inoculation by microorganisms. Figure 8. Observation of cleaned and disinfected PUR coupons placed on malt extract agar (Petri dish 9 cm in diameter), incubated for 6 weeks at 27 °C/80% relative humidity. Before depositing on agar plates, the coupons were cleaned with distilled water and disinfected with successive baths of 70% ethanol and 1% o-phenylphenol.

Conclusions
Molds are major agents in the biodegradation of PURs. They express this activity within complex communities in soils or composts, and many of them biodegrade polyurethanes in vitro in monoculture. The fungal biodegradation of PURs is mainly linked to the joint secretion of several enzymes that cleave the urethane bond or other bonds in the polymer either by hydrolysis or oxidation. Knowledge of the mechanisms of this biodegradation can be used to develop materials resistant to fungal biodegradation that are intended for long-term exposure to microorganisms, like waterproofing coatings, or, on the contrary, to develop biodegradable PURs that are compostable or have anti-fouling properties. The development of PURs with anti-fouling properties is another key issue because microbial adhesion and the development of biofilm on polymers are essential steps in their biodegradation or the development of infections. Research must also focus on the isolation, characterization, and optimization of microbial strains or microbial consortia with Figure 8. Observation of cleaned and disinfected PUR coupons placed on malt extract agar (Petri dish 9 cm in diameter), incubated for 6 weeks at 27 • C/80% relative humidity. Before depositing on agar plates, the coupons were cleaned with distilled water and disinfected with successive baths of 70% ethanol and 1% o-phenylphenol.

Conclusions
Molds are major agents in the biodegradation of PURs. They express this activity within complex communities in soils or composts, and many of them biodegrade polyurethanes in vitro in monoculture. The fungal biodegradation of PURs is mainly linked to the joint secretion of several enzymes that cleave the urethane bond or other bonds in the polymer either by hydrolysis or oxidation. Knowledge of the mechanisms of this biodegradation can be used to develop materials resistant to fungal biodegradation that are intended for long-term exposure to microorganisms, like waterproofing coatings, or, on the contrary, to develop biodegradable PURs that are compostable or have anti-fouling properties. The development of PURs with anti-fouling properties is another key issue because microbial adhesion and the development of biofilm on polymers are essential steps in their biodegradation or the development of infections. Research must also focus on the isolation, characterization, and optimization of microbial strains or microbial consortia with high potential for the biodegradation of PURs and the optimization of composting processes. Funding: This study was part of the project "Développement de matériaux polymères d'étanchéité de bâtiments résistants à la biodégradation microbienne" funded by Association Nationale Recherche Technologie (ANRT), Cifre n • 2021/0458.