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Effect of storage time on the biodegradability of olive oil mill wastewater from the cold extraction of olive oil system


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Introduction

The olive industry is a very important economic activity in Mediterranean countries (1), including Algeria, where the olive tree is one of the most planted plants. This agriculture is concentrated in the country’s north, especially in mountainous areas (2). In addition to the production of olive oil during each season, this activity generates two kinds of waste. The first is a solid called olive pomace, and the second is a liquid called olive oil mill wastewater (OMW) or vegetation water (3). The composition of OMW is more variable. This variable is affected by the quality of the olives their level of ripeness, the extraction system, and the quality of the water added during the oil recovery stage (4). Recovery applications and assessments have adopted the physicochemical properties of treated wastewater. The variation of these characteristics is determined by the variety of olive, geographical and climatic conditions, fertilizer use, and process of pressing olives (4, 5). The major waste product from the extraction of olive oil in heavily polluted acidic liquid form is OMW. Because of the presence of tannins and phenolic compounds of low molecular weight (6, 7), it has an extreme purple-brown or brown-red to black appearance and an olive oil odor. Its composition is variable and complex, primarily consisting of sugars, lipids, polyalcohols, proteins, organic acids and polyphenols (8). It is considered as one of the most contaminated and hazardous food industry residues to the environment (9), especially from producing countries (10). This is due to its diverse organic structure, vast quantity, and complexity in treating, as well as the lack of practicable or cost-effective OMW treatments (5, 1). Therefore, it must be disposed of by dumping it immediately into the air, most often in waste streams, storing it in evaporation ponds, or spreading it out to the ground, resulting in soil blockage, surface and ground water pollution, and the release of unpleasant odors. Much of this has a detrimental impact on the environment (12, 13, 14), as he has recently noticed. Every year, there is a rise in olive production and the establishment of mills as a result of increased use of olive oil due to its health benefits (15). This increase in production leads to an increase in waste, particularly when comparing modern techniques for extracting olive oil to older techniques (16). It entails an uptick in emissions and significant environmental disruption. The toxicity of OMW is mostly due to their high content of non-biodegradable organic matter, which makes them resistant to natural degradation (17). Annual volumes of olive pomace is estimated to be 180,000 tons; a ton of olives yields 450 liters of OMW under traditional pressure and 600 to 1200 liters under modern pressure (18). For many years, the primary goal of much research has been to reduce the polluted effects of OMW by identifying appropriate alternatives and treatment approaches. They have embraced and improved a wide range of relevant approaches and technologies, including thermal treatments (19), physicochemical treatments (20), biological treatments (21), and physical treatments (2) and evaporation ponds, which are still the most commonly used technique due to their simplicity (12,16). However, although all of the procedures and approaches that have been tested and evaluated for OMW treatment have proved to be technically reliable, they can not be used because they are prohibitively costly.

Before conducting or experimenting with any waste treatment, physicochemical analyses are required to know its properties in order to select the most appropriate method of treatment, and this is to avoid having a negative impact on the environment rather than solving the problem (23). In this study, we attempted to determine the effect of storage time on the biodegradability of OMW in three different samples (Zlitni, Abani varieties, and bi-varietal mixture 50%-50%) from the cold extraction system of olive oil in Khenchela, Algeria’s northeastern region.

Materials and Methods
Origin of the olive mill wastewaters

During the olive harvest season, OMW fresh sampling was conducted in a modern cold extraction oil mill where the extracting temperature does not exceed 25 °C, located in Baghai, Khenchela (35°31’19 “N, 7°6’52” E, 886m a.s.l.) in northeastern Algeria (January 2019). The samples were taken from the liquid effluent collection tank immediately just after olive press, put in clean plastic cans rinsed with the OMW to be tested, and then closed without any alteration or treatment. They were stored at room temperature in the dark. Each analysis is carried out three times.

Different parameters were examined at different storage times: t0: time just after olive oil extraction, t1 (1M): one month of storage, t2 (2M): two months of storage, t3 (6M): six months of storage, and t4 (12M): twelve months of storage.

Physicochemical parameters

Seventeen (17) physicochemical parameters were studied, including pH, electrical conductivity EC, lipid content, water content (H2O%), dry matter (DM), total suspended solids (TSS%), organic matter (OM), mineral matter (MM), volatile matter (VM), total organic carbon (TOC), total kjeldalh nitrogen (TKN), C/N, biological oxygen demand (BOD5), chemical oxygen demand (COD), total oxidizable matter (TOM), biodegradability index (BI), and BOD5/COD.

pH

The pH was measured directly in the sample using a pH meter form (AdwaAD1000) with pH buffer solutions 4, 7, and 10, according to Rodier’s method (24).

Electrical conductivity (EC)

It was measured following the method of Rodier (24), for samples filtered and centrifuged without making a dilution, using a conductivity meter type (inoLab WTW). The results were expressed in millisiemens per centimeter (mS/cm).

Lipid content

Following the method of D’Annibale et al. (21), lipid content was determined gravimetrically after hexane extraction. 20 mL of OMW was mixed with 30 mL of n-hexane, the mixture was vigorously mixed with a vortex type (VELP scientifica ZX3) in a 100 mL separating funnel, then centrifuged in a centrifuge type (SIGMA 2-16K) for 5 min at 3000 t/min. The three-hexane phases were combined and the solvent was evaporated at 79 °C in a rotary evaporator type (HAHNSHIN SCIENTIFICCO), dried at 100 °C in an oven and then cooled in a desiccator for 30 min. The drying was repeated until a content weight is obtained. The results were expressed in percent (%).

Water content (H2O %)

According to the method of Gortzi et al. (25), it was measured by drying at 105 °C for 24 hours in an oven model (memmert) and weighting the difference between the dry and wet samples. The results were expressed in percent (%).

Dry matter DM

The dry matter rate was determined by the weight difference between the OMW (100%) and the content (H2O %).

DM % = 100 % - % H2O (25).

The results were expressed, after applying the rule of three, as grams per liter (g/L).

Total suspended solids TSS (%)

The total suspended solids (TSS %) were obtained according to the method of Assas et al. (26) after drying overnight at 105 °C and then weighing (AFNOR NF T90- 105). The results were expressed in percent (%).

Organic matter (OM)

The content of organic matter was obtained by deduction between the dry weight of the OMW and its weight after calcination (mineral matter) (27). The results were expressed as grams per liter (g/L).

Mineral matter (MM)

It was performed according to Pauwels et al. (27). The dry OMW sample was calcined in a muffle furnace type (Nabertherm) at 550 °C, for 24 hours. After cooling in a desiccator, the ashes were weighed and constitute the mineral matter. We calculated it according to the formula: MM = (M2 - M0) / V x 1000, with:

MM: ash content (g/L), M0: empty capsule mass (g),

M2: capsule mass with calcined dry matter (g), V: volume of the test sample (ml).

The results were expressed as grams per liter (g/L).

Volatile matter (VM)

It was determined by making the difference between the dry matter obtained and the ash residue from calcination at 550 °C in a muffle furnace for 24 h. It was expressed in g/L relative to the dry weight (27). The results were expressed as grams per liter (g/L).

Total organic carbon (TOC)

It was determined according to AFNOR standard AFNOR T90-110 (28). It was determined from the rate of organic matter using the formula:

TOC% = %OM / 1.725

The results were expressed in percent (%).

Total Kjeldahl Nitrogen (TKN)

It was determined according to AFNOR standard AFNOR T90-110 (28), using the Kjeldahl method with some modifications. Introduce 5 mL of raw OMWW with 7.5 g catalyst (CuSO4 + K2SO4) and a little selenium in a matrass. Add 10 mL of H2SO4 and 10 mL of oxygenated water 30% (H2O2) as anti-foaming. Put some glass balls as shockproof.

Heat to a temperature of 100 °C for a while to prevent the foam from overflowing and continue heating until it disappears and the contents are charred. Then increase the mineralization temperature to 400 °C until the appearance of a clear and limpid green coloration, continue heating for 30 min then let cool. Distillation was done using soda (32%) and distilled water in an automatic distillation apparatus. The distilled ammonia is trapped in an Erlenmeyer flask containing 20 mL of boric acid 4%, then quickly titrate with sulfuric acid (H2SO4) (N/50) up to the initial pH of boric acid. The nitrogen level was calculated according to the following formula:

% N2 (g) = (V1 * 0.014*100*N)/V0

N: normality of the sulfuric acid N/ 50.

V0: sample volume in ml (5mL).

V1: volume in ml of the sulfuric acid solution used for the titration.

The results were expressed as grams per liter (g/L).

Carbon to nitrogen mass ratio (C/N)

Determined by method of AFNOR (29). The carbon to nitrogen ration is an indicator of the ability of an organic product to decompose more or less quickly in the soil.

C/ N > 25: Microorganisms will draw on soil reserves instead of releasing them.

C/N < 25: Microorganisms will release excess nitrogen available to plants.

Biological oxygen demand (BOD5)

It was determined following the method of Rodier (24), using a BOD meter type (VELP Scientifica) in a thermostatically controlled enclosure type (AQUA LYTIC) for the biological oxygen demand BOD5 (AFNOR T90-103). The results were expressed as grams per liter (g/L).

Chemical oxygen demand (COD)

The chemical oxygen demand COD is determined on raw OMW samples according to the AFNOR NF T90-101 standard, using a COD meter type (VELP Scientifica), using potassium dichromate as described by Rodier (24). The results were expressed as grams per liter (g/L).

Total oxidizable matter (TOM)

It constitutes the main part of the biodegradable part of the organic pollution released; it was determined by calculating the formula (24):

TOM (g/L) = (2 BOD5 + COD) /3

The results were expressed as grams per liter (g/L).

Biodegradability index (BI)

It was determined by calculating the ratio of COD/BOD5, an indicator of the importance of pollutants with little or no biodegradation (24).

BI = COD/BOD5

If:

B I> 6: Hardly biodegradable substrate

3 < BI < 6: Partially (or less easily) biodegradable substrate

BI < 3: Very easily biodegradable substrates.

BOD5/COD ratio

An index that gives an idea of the level of pollution presented by the liquid effluents.

BOD/COD > 0.5: effluent treatable by biological processes.

0.2 < BOD/COD < 0.6: feasibility of treatment using selected microbial strains.

BOD/COD < 0.2: biological treatment impossible (30).

Statistical analyses

All data was analyzed by two-ways ANOVA. Correlations between some parameters were determined using Pearson’s simple correlation test. Means were compared using Duncan’s test at p<0.05 level of significance by means of SPSS 20 for Windows. The principal Components Analysis (PCA) test was performed using XLSTAT software version 2014.5.03 (Addinsoft).

Results
Effect of the genotype, time, and their interaction on the measured parameters

The analysis of variance (Table 1) showed the existence of a very highly significant genotype effect on the measured parameters (pH, EC, Lipids, TSS, Water, DM, VM, TKN, C/N, COD, BOD5, and TOM) with (P < 0.001), significant on MM with 0.01< p < 0.05. Additionally, the time effect was also highly significant on all of the measured parameters (pH, EC, Lipids, TSS, Water, DM, VM, TKN, C/N, COD, BOD5, MM, BI, TOM, and BOD5/COD) with (p < 0.001) and excepted for the two parameters OM, TOC showed a significant effect at 0.001 < p < 0.01.

Results of variance analysis of the genotype effects, time and their interaction on some measured parameters

ANOVA pH EC COD BOD5 BI TOM BOD5/COD
Genotype (G) *** *** *** *** ns *** ns
Time (T) *** *** *** *** *** *** ***
G x T *** *** * ns ns * ns
Error 0.000 0.000 432.822 118.803 0.092 142.061 0.004

ns, not significant, *, **, *** significant at p<0.05, p<0.01, and p<0.001, respectively.

The decrease rates of the Zlitni, combination, and Abani varieties were 1.68, 1.88, and 2.03 units, respectively. A comparison of average values revealed that the Zlitni variety was more acidic than the mixture and the Abani variety, with values of (4.40, 4.42, and 4.82, respectively).

Effect on electrical conductivity

The electrical conductivity of the samples decreased after 12 months of storage (Fig. 1). EC was lowered by 90.82%, 87.15%, and 84.7% for the Abani, Zlitni, and combination, respectively. The average values registered for Abani, the combination, and Zlitni are 14.72, 14.33, and 12.83 mS/cm, respectively.

Figure 1

Linear regression representing the pH and EC of the tested OMWs within time of the storage. Z, A, and M correspond to Zlitni, Abbani, and Mixture, respectively. t0, t1(1M), t2(2M), t3(6M), and t4(12M) correspond to different storage time.

There was a highly significant interaction effect (G x T) on the calculated parameters (pH, EC, Lipids, Water, and DM) with (p < 0.001). This interaction had a significant effect to 0.001 < p < 0.01 on TSS and to 0.01 < p < 0.05 significant effect on the parameters (MM, TKN, COD and TOM).

The (G x T) correlation, on the other hand, had no impact on the calculated parameters (VM, OM, TOC, C/N, BI, and BOD5/COD). For the varieties Zlitni, Abani, and their combination, the means of the calculated parameter BI demonstrated a very highly important relationship with storage time. Consequentially, it was insignificant for the genotype effect and the relationship (G x T).

At first overview, the OMW tended to have a reddish-brown coloration, which darkened with storage, with a cloudy look and heavy smell reminiscent of olive oil, which become stronger with storage time.

The physicochemical properties of OMW were done basically by the variety and the extraction system. Table 1 showed the average compositions of the wastewater from the Zlitni and Abani types, as well as their mixture, used in this study. The mean effect of genotype, time, and their interaction on lipid contents, TSS percent, and MM revealed 11 groups, water content 14 groups, DM 13 groups, MV and C/N 10 groups, OM 4 groups, TOC 5 groups, and TKN 12 groups.

Effect on pH

The obtained results revealed that the pH values of the three samples increased gradually over a period of 12 months of storage (Fig. 1).

Effect on lipid content

During 12 months storage period, the lipid content of Zlitni, Abani, and the mixture decreased by 96.95, 88.93, and 95.34%, respectively. The OMW analyzed was low in lipids. According to a comparison of average values, the fattest rich OMW were those of variety Abani rather than the mixture, and the lowest is Zlitni, with the average values registered being (1.58, 1.44, and 1.33% ).

Effect on TSS%

TSS values lowered by 33.67, 32.45, and 28.71% after 12 months of storage for Zlitni, Abani, and the mixture, respectively. According to the results obtained, the effluents studied were not very high in TSS. The average values received, sorted from most charged to least charged, were Abani (1.02%), the combination (0.91%), and Zlitni (0.91%) (0.87%).

Effect on water content

The water content gradually increased over 12 months storage period. The average was rising by 18.13, 19.38, and 18.56% for Zlitni, Abani, and the combination, respectively. The average values derived from more or less charge of water are 89.38, 88.86, and 88.48% for Zlitni, the combination, and Abani, respectively.

Effect on dry matter

During 12 months of storage, dry matter content decreased gradually. It was decreased by 85.65, 83.68, and 88.03% for Zlitni, Abani, and the combination, respectively. The results indicated that the effluents were high in dry matter. The Abani variety had the highest average value, followed by the mixture and then Zlitni, with the following values (117.17, 111.43, and 107.7 g/L).

Effect on organic matter

Organic matter reduced by 3.86, 5.03, and 4.14% with a storage period of 12 months for Zlitni, Abani, and the mixture, respectively. According to the findings, the OMW was loaded with organic matter. The three sample mixtures, Abani and Zlitni, had almost the same content with the following average values (82.44, 81.61, and 81.98 g/L).

Effect on mineral matter

Mineral matter slowly degraded over 12 months storage period. For Zlitni, Abani, and the mixture, the decreasing rates were approximately 24.57, 29.90, and 33.45%, respectively. For the three samples, the values observed during the analysis were nearly identical. The average values obtained for Abbani, the mixture, and Zlitni are 23.07, 22.86, and 21.85 g/ L, respectively.

Effect on volatile matter

The results obtained showed that volatile matter decreased by 96.08, 93.13, and 97.40% during 12 months storage period for Zlitni, Abani, and the mixture, respectively. Furthermore, the OMW tested were very high in volatile matter, demonstrating the organic origin of OMW. The average values were (70.49 g/ L from Abani, 66.20 g/L from Zlitni, and 65.56 g/L from the mixture, respectively).

Effect on NTK

During 12 months storage period, the NTK content decreased. It was reduced by 29.60% for Zlitni, 43.50% for Abani, and 41.17% for the combination, respectively. According to the findings, OMW samples were very high in nitrogen. It registered the highest values in the mixture of the two varieties, then Abani and Zlitni with average values of (2.20, 1.90, and 1.71 g/ L, respectively).

Effect on TOC %

TOC% decreased by 3.85, 5.03, and 4.15% after 12 months of storage for Zlitni, Abani, and the mixture, respectively. The results indicated that the TOC content was high in the liquid effluents tested. In all three experiments, we founded almost identical results. The order’s average values are 47.79, 47.31, and 47.52% from the mixture, Abani, and Zlitni, respectively. Effect on C/N

According to the results obtained, the rate in this ratio increased gradually with the duration of 12 months of storage. Zlitni, Abani, and the mixture all increased by 46.55, 68.12, and 62.64%, respectively. In addition, the Zlitni variety had the highest average value (28.77), followed by Abani (26.19) and then the mixture (22.56).

Effect on BOD5

During 12 months storage period, BOD5 values declined by 40.65, 48.38, and 46.42% for Zlitni, Abani, and the Mixture, respectively.

The studied OMW had important BOD5 values, indicating that they are highly filled with biologically oxidizable organic matter. The average values revealed that the OMW of the mixture is higher (93.59 g/L) than (81.92; 62.27 g/L) for Abani and Zlitni, respectively.

Effect on COD

COD values gradually decreased during storage, indicating that organic matter was degrading. The decreasing rates for Zlitni, Abani, and the Mixture, respectively, were 71.18, 71.11, and 69.53%.

According to the findings, the OMW analyzed had a very high oxygen demand for total oxidation of organic matter. The highest average values were found in the mixture (237.87 g/ L), Abani (209.8 g/L), and Zlitni (157.8 g/L), in that order.

Effect on BI

The implications of this ratio indicated the significance of low or biodegradable pollutants. According to the findings (Fig. 4), this ratio decreased steadily with storage time by 50.58, 43.40, and 43.13% for Zlitni, Abani, and the mixture, respectively. Furthermore, BI was almost identical in all three samples. The average values found are (2.43), (2.46), and (2.48) from Zlitni, the mixture, and Abani, respectively.

Figure 2

Effect of interaction (G x T) on BOD5 of the tested OMWs and their homogenous groups. Z, A, and M correspond to Zlitni, Abbani, and Mixture, respectively. t0, t1(1M), t2(2M), t3(6M), and t4(12M) correspond to different storage time. Column values with different letters are significantly different at p<0.05, according to Duncan’s multiple range test.

Figure 3

Effect of interaction (G x T) on COD of the tested OMWs and their homogenous groups. Z, A, and M correspond to Zlitni, Abbani, and Mixture, respectively. t0, t1(1M), t2(2M), t3(6M), and t4(12M) correspond to different storage time. Column values with different letters are significantly different at p<0.05, according to Duncan’s multiple range test.

Figure 4

Effect of interaction (G x T) on BI of the tested OMWs and their homogenous groups. Z, A, and M correspond to Zlitni, Abbani, and Mixture, respectively. t0, t1(1M), t2(2M), t3(6M), and t4(12M) correspond to different storage time. Column values with different letters are significantly different at p<0.05, according to Duncan’s multiple range test.

Effect on TOM

The results showed that oxidizable matter degrades during storage time (Fig. 5). TOM values for Zlitni, Abani, and the Mixture decreased by 59.90%, 62.22%, and 60.40%, respectively, from t0 to t4. Moreover, TOM was included in a large amount of the OMW samples studied. The average values were higher in the mixture (141.68 g/L), Abani (124.55 g/L), and Zlitni (94.11 g/L), in that order.

Figure 5

Effect of interaction (G x T) on TOM of the tested OMWs and their homogenous groups. Z, A, and M correspond to Zlitni, Abbani, and Mixture, respectively. t0, t1(1M), t2(2M), t3(6M), and t4(12M) correspond to different storage time. Column values with different letters are significantly different at p<0.05, according to Duncan’s multiple range test.

Effect on BOD5/COD

We showed that this ratio improved over the period of 12 months of storage (Fig. 6). This average raised by 110.34, 78.12% for Zlitni, Abani, and the mixture, respectively. The values revealed that this ratio was almost identical in all samples. The average values obtained in the order were Zlitni (0.44), Abani (0.43), and the mixture (0.43). Multivariate analysis (PCA).

Figure 6

Effect of interaction (G x T) on BOD5/COD of the tested OMWs and their homogenous groups. Z, A, and M correspond to Zlitni, Abbani, and Mixture, respectively. t0, t1(1M), t2(2M), t3(6M), and t4(12M) correspond to different storage time. Column values with different letters are significantly different at p<0.05, according to Duncan’s multiple range test.

The search for links between the genotypes of the water resources and their parameters measured during their storage (after time of 0, 1 month, 2 months, 6 months and 12 months) was studied through to the main PCA component analysis (Fig. 2). The projection of the variables (The parameters) and of the individuals (The genotypes) was carried out on the two axes which represent 88.17% of the total variance. The first two axes hold respectively 78.51% and 9.66% of information. Axis 1 integrated the information provided by most of the measured parameters (pH, EC, Lipids, TSS, DM, VM, TKN, COD, BOD5, MM, BI, TOM, OM and TOC) of the Zlitni varieties, Abani and their mixture after 0 months, 1 month and 2 months of their storage (t0, t1, t2). These parameters were positively correlated with this axis. The group composed exclusively of VM, DM, and BI parameters of the varieties tested in addition to their mixture and measured immediately after sampling was positively correlated to axes 1 and 2 of the PCA. In addition, it was opposed along these two axes of the PCA and to the group consisting of the water parameter measured after 6 months of storage varieties tested with their mixture. Axis 2 of the PCA integrated the information provided by two groups. The third group had a positive correlation with this axis (2) and a negative correlation with axis 1. This group included the two parameters C/N and BOD5/COD of the varieties Zlitni, Abani, and their mixture, which were determined after one year (12 months) of storage. This group was opposed along this axis to the group composed of the parameters (pH, EC, Lipids, TSS,, DM, VM, TKN, COD, BOD5, MM, BI, TOM, OM, and TOC) of the Zlitni varieties, Abani, and their mixture, which were measured after one month of storage (t1) and were positively correlated with axis 1 and negatively correlated with axis 2.

Figure 7

Projection of the interaction (time, genotypes and parameters measured on the plane (1 x 2) of the principal component analysis (PCA). Z, A, and M correspond to Zlitni, Abbani, and Mixture, respectively. t0, t1(1M), t2(2M), t3(6M), and t4(12M) correspond to different storage time.

The decrease in parameters (pH, EC, Lipids, TSS, DM, VM, TKN, COD, BOD5, MM, BI, OM, TOM, and TOC) of Zlitni and Abani varieties and their mixture are positively correlated with storage time and was extreme after 6 and 12 months. On the other hand, the parameter BOD5/COD increased during storage, indicating that this increase is positively correlated with time, as it gave higher values after 6 and 12 months, as explained.

Discussion

The rate of biodegradability of OMW was not constant during the storage time because OMW, due to their organic and mineral charges, provided a favorable medium for the survival of microorganisms. Microorganisms that consume it with the oxygen dissolved in this liquid effluent discover the organic matter. Furthermore, changes promote and affect microbial habitat, while organic degradation with a various enzymatic activities was already in progress (31,32).

The OMW occurred as a reddish-brown to black aqueous and viscous residual liquid with a heavy olive odor. It comprised a diverse range of organic and mineral compounds of varying composition and concentration. This heterogeneity was primarily the product of the following factors: olive-ripening stage, soil and climate conditions, variety of olives, cropping system, duration and storage conditions of the olives before crushing, olive oil extraction process, which represents the most determining factor (33).

pH findings were consistent with those in other studies (16,23,34,35,36). According to the literature, the presence of organic acids (37) and fatty acids such as palmitic acid, oleic acid, linoleic acid, and arachidonic acid (38), as well as sugar fermentation (39) and auto-oxidation and polymerization reactions that transform phenolic alcohols to phenolic acids (16). These reactions were manifested by a modification in the OMW’s initial coloration to a very dark black color (40). Indeed, our effluents get a reddish-brown color that darkens significantly during storage. As a result, microbial reactions, oxidation, and fermentation probably induced the significant decrease in pH during storage.

The importance of pH was critical for the growth of microorganisms, which had an optimum pH range of 6.5 to 7.5. When the pH was less than 5 or greater than 8.5, the growth of microorganisms was directly inhibited, making biological treatment of raw OMW very complicated (16).

The means of the measured parameters of the varieties Zlitni, Abani and their mixture during storage and homogenous groups

Genotype Time Lipids (%) TSS (%) Water (%) DM (g/1) MM (g/1) VM (g/1) OM (g/1) TOC (%) TKN (%) C/N
Zlitni to 1.97±0.02d 0.98±0.03cd 83.26±0.05k 167.33±0.57c 24.38±0.33abc 142.95±0.47b 84.53±1.53ab 49±0.89ab 1.96±0.06de 24.94±1.20def
tl(lM) 1.74±0.04f 0.93±0.01ef 84.24±0.06i 157.56±0.66e 23.48±0.81bc 134.08±1.33d 81.19±2.80abc 47.07±1.62abc 1.89±0.02e 24.82±0.98def
t2(2M) 1.6110.04g 0.90±0.01ef 85.53±0.04g 144.63±0.47g 22.23±0.83cd 122.39±0.99f 84.67±1.44a 49.08±0.83a 1.83±0.02ef 26.77±0.57cde
t3(6M) 1.2410.04i 0.8910.01fg 95.50±0.04d 44.96±0.41j 20.75±1.52def 24.21±1.81h 78.21±1.28C 45.34±0.74c 1.47±0.02gh 30.78±0.89c
t4(12M) 0.06±0.00k 0.65±0.00i 98.36±0.02a 24±3.90i 18.39±1.50fg 5.60±3.88j 81.26±2.50abc 47.11±1.44abc 1.38±0.49gh 36.55±10.87ab
Abani to 2.35±0.05a 1.14±0.03a 82.16±0.2n 178.33±2.08a 26.65±0.99a 151.67±2.25a 85.34±1.54a 49.47±0.89a 2.23±0.03bc 22.12±0.73ef
tl(lM) 2.07±0.05c 1.12±0.02a 83.08±0.05i 169.20±0.5c 25.72±1.40ab 143.47±1.85b 79.94±0.21abc 46.34±0.12abc 2.19±0.00cd 21.12±0.02ef
t2(2M) 1.87±0.02e 1.06±0.01b 84.22±0.04i 157.73±0.4e 25.0811.91ab 132.65±1.84d 80.91±0.92abc 46.90±0.53abc 2.17±0.02cd 21.55±0.46ef
t3(6M) 1.36±0.04h 0.98±0.00cd 94.85±0.05f 51.46±0.5h 19.18±1.76efg 32.28il.26g 80.81±1.76abc 46.84±1.02abc 1.62±0.02fg 28.93±1.09cd
t4(12M) 0.26±0.02j 0.77±0.02h 98.09±0.03b 29.10±0.3k 18.68±0.71efg 10.41±0.94i 81.04±0.49abc 46.98±0.28abc 1.26±0.01h 37.19±0.42a
Mixed to 2.15±0.05b 1.01±0.07bc 82.58±0.07m 174.16±0.7b 25.47±1.53ab 148.69±2.05a 85.62±0.33a 49.63±0.19a 2.55±0.04a 19.41±0.23f
tl(lM) 1.94±0.02d 1.03±0.01b 83.66±0.04j 163.33±0.4d 26.04±0.45a 137.29±0.62c 82.73±4.20abc 47.96±2.43abc 2.49±0.04a 19.23±0.90f
t2(2M) 1.74±0.04f 0.95±0.01de 84.91±0.03h 150.83±0.3f 24.88±0.99ab 125.95±0.87e 83.24±1.19abc 48.25±0.69abc 2.44±0.01ab 19.75±0.32f
t3(6M) 1.2710.03i 0.85±0.01f 95.20±0.02e 48±0.2i 20.96±2.22de 27.03±2.12h 78.53±9.77bc 45.52±5.66bc 1.99±0.02de 22.81±2.96ef
t4(12M) 0.10±0.01k 0.72±0.01i 97.91±0.02c 20.83±0.2m 16.9511.35g 3.8711.64j 82.07±1.20abc 47.57±0.69abc 1.50±0.01g 31.57±0.37bc
ANOVA Genotype (G) *** *** *** * ns ***
Time (T) *** *** *** *** *** *** ***
GxT *** *** *** ns ns ns * ns
Error 0.001 0.001 0.005 1.508 1.777 3.225 9.535 3.204 0.017 8.918

ns, not significant, *, **, *** significant at p<0.05, p<0.01, and p<0.001, respectively.

For the electrical conductivity, the obtained results showed that the OMW had a high electrical conductivity due to the rich mineral load (12). Our results were consistent with those of Zaier et al. (23) (EC = 1–13 mS/cm), Ouabou et al. (35) (EC = 16.14 mS/cm), and Belaid et al. (34) (EC = 15–15.1 mS/cm). This disparity in electrical conductivity was due to the normal mineral salt content of olives (9, 20).

According to Achak et al. (9), conductivity was closely related to the quantity and composition of dissolved substances. In the case of OMW, this conductivity ranged between 18 and 50 mS/ cm. The decrease in electrical conductivity rate with storage time may be attributed to the activity of bacteria qualified as prototrophs degrading the mineral elements in OMW.

The lipid level in OMW, in general, ranging from 0.03% to 4.25% in the literature. The findings agreed with those of many other researchers, including Kapellakis et al. (10) (lipids = 0.5–2.3%) and Esmail et al. (16) (lipids = 1–2.5%), Benamar et al. (14) (0.03–1.1%), and Mohawesh et al. (1). (0.97%). The level of lipids present in OMW was determined by the olive oil extraction system.

When opposed to the conventional method, the centrifugation process produces low rates. The difference in lipid content is due to the olives’ consistency, degree of ripening, and crushing process (38).

Because of the presence of the oily fraction, the OMW tested had a viscous texture. This viscosity decreases with storage time. It formed a lipid layer on the surface of OMW, perhaps limiting natural evaporation.

According to the literature, the presence of fat matter allows the forming of a layer on the surface of the water, preventing proper oxygenation and light passage and obstructing the natural growth of flora and fauna within rivers. Soil bacteria that developed spores are inhibited by fatty acids and their derivatives. The decrease in lipid levels may be attributed to lipolysis, which eventually degraded fat during storage.

In addition, variations in suspended matter content can be attributed to climatic and geographical factors, botanical variations, the stage of olive ripening, and the oil extraction process (41). They were comparable to the results of D’Annibale et al. (21) (0.04–1.04%). The TSS of OMW may be declined as a result of settling. This was most likely due to the effect of variety, maturity level, and agitation induced by the unloading of the OMW. The decrease in TSS level was probably due to the fermentation reaction and auto oxidation.

Also, for the water content, several researchers had comparable findings, including Kapellakis et al. (10) (83–92%), Ouabou et al. (35) (88%), Ouabou et al. (42) (86–87.6%), and Noubigh et al. (8) (83–94%). According to Nefzaoui (3), OMW was composed of 40 to 50% of vegetable water derived from the fruit and the remainder manufacturing water added during the crushing process. Procida and Ceccon (43) showed that the high humidity level of OMW was explained by the water present in the olives on the one side, and the water added during the olive oil extraction process on the other. The increase in humidity was caused by microbial activity, which produces water molecules as well as H2 and CO2 gases.

The obtained results for the dry matter were closer to those of Ouabou et al. (35) (138 g/L) and Ouabou et al. (42) (between 138.44 and 240 g/ L). Variations in dry matter quality, according to El-Abbassi et al. (41), can be caused by climatic and geographical conditions, botanical variations, the stage of olive ripening, and the oil extraction process.

This decrease during the storage period was most probably due to matter deterioration caused by the microbial load in the vegetable water.

For the organic matter, the results obtained were superior to those obtained by Zaier et al. (23) (41.2–65.9 g/L) and closer to those obtained by Rajhi et al. (36) (89.59 g/L). The presence of macromolecules such as polysaccharides, lipids, proteins, and a variety of monocyclic and polymeric aromatic molecules was primarily responsible for the organic charge (20).

The slow degradation of macromolecules was responsible for the decrease in organic matter degradation rate. Microbial growth required energy, which was provided by organic molecule degradation.

The mineral matter results were consistent with those of Ouabou et al. (35) (24 g/L), Ouabou et al. (42) (22.69–24.35 g/L), and Belaid et al. (34) (10–25 g/L). The degree of ripening and the variety of olives illustrated the difference in mineral matter (41).

The slow decrease may be due to bacteria’s inability to degrade it, as they require mineral elements to expand.

Effect on volatile matter

The gradual decrease in volatile matter could be due to bacteria, which can degrade many hydrocarbon substances such as organic acids, alcohols, sugars and polyholosides. These were closer to that observed by Zaier et al. (23) (49.7–81.4 g/L), Belaid et al. (34) (20–21.5 g/L), and Hamdi (37) (55 g/L). This difference was due to climatic conditions, olive oil extraction methods as well as the storage time of the olives before crushing (41).

The results of NTK were within the ranges reported by Capasso et al. (4) (1.2–2.4%) and Kapellakis et al. (10) (1–3 g/L). This distinction may be attributed to the soil’s natural abundance of nitrogen, which is retained in the fruit, or to the use of chemical fertilizers (45).

The continuous decrease is most possibly due to protein synthesis, which requires nitrogenous substances. The majority of bacteria obtain their nitrogen from other inorganic compounds (ammonia, ammonium salts, nitrites, nitrates) or from organic sources (amine group of organic compounds).

For the TCO%, they were higher to those found by Belaid et al. (34) (13–15 g/L) and Mekki et al. (46) (17.6%). These results were due to its richness by organic matter and the metabolism, which degraded and released it during CO2, ethanol and lactic acid reactions, further due to the polymerization.

The rise in the rate of C/N is attributed to the samples’ low biodegradable organic load and total organic carbon load.

The findings were closer to those found by Mekki et al. (46) (35.20) but lower than those obtained by (12). (50.50).

The results obtained for BOD5 are almost equivalent to those obtained by Zaier et al. (23) (65.87–86.71 g/L) and Ouabou et al. (42) (12.50–62.50 g/L). The presence of organic matter in the OMW was probably explained these high values.

This gradual decline during storage may be due to the microbial load and glucose metabolism, which releases gas, CO2, ATP, H2, alcohols, and H2O, as well as the use of biologically degradable molecules such as H2O and CO2.

Moreover, for COD, several researchers had determined similar findings. Zaier et al. (23) measured 219.34–286.3 g/L, Ouabou et al. (42) measured 340–374 g/L, Hamimed et al. (47) measured 189.70 g/L, and Benamar et al. (14) measured 227.33 g/ L. This decrease was caused by autoxidation and polymerization reactions, as well as the breakdown of recalcitrant molecules into biodegradable molecules or mineral compounds like H2O and CO2.

In addition, BI results fall within the range of the findings of Mekki et al. (46) (4) and Zaier et al. (23) (3.301–3.342). Moreover, it was lower than (4.48) that found by El-Rhaouat et al. (48). After one month of storage, we can concluded that even the OMW had a heavy organic load and was quickly biodegradable.

For TOM and BOD5/COD successively, the findings were higher than of those found by El-Rhaouat et al. (48) (TOM = 50.91 g/L) and (BOD5/COD = 0.24).

Finally, based on the results of multivariate analysis (PCA), the biodegradability of OMW was probably due to the degradation of organic matter, which provided as a source of food for microorganisms that consume oxygen from the medium, which was becoming increasingly scarce (31).

Conclusion

Olive oil mill wastewater is one of the most important problems facing olive oil-producing countries. Since it is rejected without treatment, it causes damage to the environment because its characteristics are very important in the treatment of these effluents. The findings obtained during this study indicate that there is variability in the proportions of the effluent components of the two-variety study samples separated and combined. The storage time effect also indicates a very highly significant difference in the rate constituents of the same variety. The variability of the results obtained is due to a difference in the variety of olive, ripening stage, time, place and techniques of storage before the crash, duration and temperature of storage of OMW. The biodegradability of OMW is mainly due to the organic load rate, the microbial load, the acidity of the environment, the variety of olives, the storage conditions and the storage time. We find that OMW acidity increases in proportion to the storage time and is lowly biodegradable directly reduced with storage time, which includes the selection of the correct treatment process.

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