Introduction

Rearing aquatic animals and plants is understood as aquaculture, ranging from fish cultivation in naturally formed ponds of rural zones to intensified complex commercial fish culture tanks of fiberglass. On a global scale, it is seen that there was a rapid growth in aquaculture. The production of aquaculture enhanced to more than 50 million presently against its production less than a million during 1950. Further, aquaculture production at a global scale grew at 8–14% per annum compared to only 1.5% of fish captures. It is estimated that the growth of aquaculture will reach 109 million tonnes by 2030, accounting for a 37% increase compared to 2016. Fisheries and its allied resources encapsulate a wide variety of food sources feeding a more significant portion of the population globally, apart from the magnificent employment sector (Zhou 2017; Joseph et al. 2021; Rotter et al. 2021).

With this tremendous increase in production, equal amounts of wastewaters are also generated from this sector. Concern over the wastewaters generated is due to its characteristics of having high organic content, oil, and grease, and salts that make their treatment challenging (Dhanke et al. 2019). These characteristics call for the mandatory treatment of these wastewaters toward maintaining quality and acceptability. Several treatment methods were developed and adopted for improving water quality, reducing water usage but were differed owing to fluctuating levels of success. On the other hand, water shortages, land costs, stringent enhanced regulations have made it necessary to develop an efficient, improved treatment method. Studies have stated that the discharges from aquaculture possess greater concentrations of ammonia and PO43− along with pathogens (Lin et al. 2003; Yerlikaya et al. 2021). Ammonia is toxic to fish, which is limited to only 2 mg/L in aquaculture wastewaters. Still, it is generally found at a higher concentration, while enhanced concentrations of PO43− result in the rapid growth of unwanted macrophytes and algae, leading to eutrophication (Ngatia et al. 2019; Karnena and Saritha 2020; Alishahi and Aïder 2012).

Although progress toward treatment processes for phosphorus reduction is made, many efforts and research are required toward efficient treatment. It is also to be noted that much phosphate concentration exists in settleable and colloidal associated solids fractions. Hence, treatment systems that effectively remove solids are needed to be made (Sitek 2020). Conventional treatment processes for aquaculture wastewater are not feasible due to the generation of toxic residue, capital investment, and operational expertise requirements. Coagulation is understood to be the most accepted treatment for the removal of colloidal particles.

Further, coagulants can also remove the suspended mineral particles as well as reduce turbidity. Previous studies have shown that conventional coagulants such as alum and ferric chloride can inactivate and precipitate inorganic phosphorus from aquaculture pond water. Though these coagulants effectively removed pollutant load, the residual aluminum had toxic effects on plants (Yang et al. 2016; Kritchenkov et al. 2021). Consequently, coagulants having properties such as being efficient, economical, non-toxic, environment friendly, and sustainable are constantly being searched. Natural coagulants are understood to satisfy all the above-said criteria.

Earlier studies have demonstrated the usefulness of natural coagulants such as chitosan (Chung et al. 2003; Yang et al. 2016). But studies on optimization and efficacy estimation concerning conventional coagulants are meager. In these lines, the aims of the present study are twofold to evaluate the competence of natural coagulant Moringa oleifera for treating aquaculture wastewater and to compare its efficiency with conventional ferric chloride. Further, the second aim is to assess the efficacy of blended coagulant M. oleifera and chitin in treating aquaculture wastewater.

Materials and methods

Acquiring and preparing coagulants

Coagulants chitin and ferric chloride were of analytical grade supplied by Coastal Enterprises of company Sigma-Aldrich, and Merck chemicals were used in the study. Seeds of Moringa oleifera were procured from the local market, cleansed and made to powder, and sieved using a 0.25-µ sieve to get a uniform size. The powder was stored in sealed polythene for further use.

Effluent sample collection

The aquaculture effluent was collected from the aquafarms located around 3–4 km from GITAM (Deemed to be University) using three 25 L jerry cans and filled to the brim to expel entrapped air within the can. The jerry-can was then corked, sealed, and refrigerated until the commencement of the experiment. Effluents were characterized as per the standard methods of APHA (APHA, AWWA, WEF 2012). All experiments were carried out in the laboratory of the Department of Environmental Science.

Jar test experiments

Experiments to determine the efficiency of coagulants were performed using conventional Jar test Apparatus (Cintex Flocculator). The experiments were carried out in batches and in triplicates which were represented as average. The individual jar was added with a 2 L sample after recording the initial temperature and adding various coagulant doses. Initial rotation of the baffles was set to 100 rpm for flash mixing for about 2 min, and the then slow mix was adopted at an rpm of 20 for about 30 min followed by settling of 30 min after the baffles are removed.

Analytical procedures

All the physicochemical analyses of all the samples are analyzed by using APHA, 2016 standard methods.

Turbidity

The nephelometric turbid meter was calibrated using 40NTU standard suspension. The sample under test is shaken thoroughly and filled in the cuvette, placed in the sample chamber. Constant value is noted down.

pH

pH was measured using a pH meter. Calibration of electrodes was carried out using 4.0 and 9.2. After rinsing with distilled water and wiping with tissue paper, the electrode is dipped into the water sample under test. At constant value, the reading is noted down.

Electrical conductivity (EC)

The conductivity cell was calibrated with 0.1 N KCl standard solution having a conductivity of 14.12 mmhos. After rinsing electrodes thoroughly using deionized water and wiping dry, the electrode is dipped into the sample under test. At constant value, the reading is noted down.

Total dissolved solids (TDS)

TDS were measured gravimetrically; a clean porcelain dish’s initial weight (A) was taken after igniting in a muffle furnace, partial cooling in the air, and cooling in a desiccator. Into this was added 100 mL (V) of filtered sample and was evaporated at 100 °C; on a water bath, it was dried in an oven at 103 °C for about an hour. The final weight (B) of the dried dish was taken after cooling in a desiccator.

$${\text{Calculations: Total dissolved solids (mg/L)}} = \frac{(A - B) \times 1000}{{\text{Volume of Sample taken}}}$$

Chlorides

A 100 mL sample was taken to a flask, and an indicator potassium chromate of 2 drops was added, after which the sample turns yellow color. This solution was titrated against 0.0141 N AgNO3 until the color changes to brick red. The consumed volume of AgNO3 was noted down (A). A blank was titrated; similarly, the volume of AgNO3 consumed was noted down (B)

$${\text{Calculation:}}\;{\text{Chloride (mg/L)}} = \frac{{(A - B) \times {\text{Normality of AgNO}}_{3} \times 35.46 \times 1000}}{{\text{Volume of Sample taken}}}$$

Total hardness

Hundred milliliters of sample was taken into conical flask to which a buffer of 2 mL was added, followed by inhibitor of 1 mL and a pinch of Eriochrome black T indicator; solution was turned into wine-red color immediately. Solutions were titrated against 0.01 M EDTA till the color changes to blue. A blank is also titrated similarly, and the volume of EDTA consumed both for sample (A) and blank (B) is noted down.

$${\text{Calculation: Total hardness (mg/l) as CaCO}}_{{3}} = \frac{(A - B) \times 1000}{{\text{Volume of Sample taken}}}$$

Calcium hardness

Hundred milliliters of sample was taken in a conical flask to which NaOH solution of 1 mL was added, followed by a pinch of murexide indicator; solution turns to pink color. Later it was titrated against 0.01 M EDTA solution till the color changes to purple. A blank is also titrated similarly, and the volume of EDTA consumed both for sample (A) and blank (B) is noted down.

$${\text{Calculation: Calcium hardness (mg/l) as CaCO}}_{{3}} = \frac{(A - B) \times 1000}{{\text{Volume of Sample taken}}}$$

Total nitrogen and total phosphorous

TN was determined using a TOC-TN analyzer (SHIMADZU, Japan), and TP was established using Hach Lange cuvette tests on the spectrophotometer (DR2000, Lange GmbH Germany).

Characterization of samples

The FTIR was analyzed using the morphology of the synthesized material examined by the Philips made CM-200. XRD patterns were determined by “PANALYTICAL X’PertPro Powder X-ray diffractometer” having a graphite monochromatic Cu Kα (λ = 1.5406°A), and sample morphology was examined with a scanning electron microscope using the FEI quanta model, JSM 7600.

Results

The efficiency of natural coagulants to treat aquaculture wastewater was investigated in the present study. The results are presented as follows.

Table 1 presents the initial analysis (raw water) of aquaculture wastewater. Values are presented as the mean of 12 samples. pH was found to be 8.33. Turbidity was found to be 2.3 NTU. The electrical conductivity of the initial analysis was found to be 9.2 µ siemens/cm2.

Table 1 Initial parameters of aquaculture waters

The total dissolved solids concentration was 4157 mg/L. The chloride content of the samples was found to be 25,000 mg/L. Concentration of total hardness was 23,000 mg/L, and that of calcium hardness was 15,000 mg/L. The concentrations of total phosphorous and total nitrogen were 11.6 mg/L and 9.6 mg/L.

Table 2 depicts the reduction of physicochemical parameters of the aquaculture water after treatment with ferric chloride. Turbidity reduction was observed maximum of 86.96% at pH 7 with a dose of 0.15 g/L. Reduction in electrical conductivity was observed to be good at pH 8 with around 99% removal. Reduction of total solids was noted to be 52–55% in all pH and dose ranges. Chloride reduction was observed to be a maximum of 36.46% at pH 6 with a dose of 0.1 g/L. Total hardness removal was negative, going to a maximum of 20.14% at pH 7 with 0.1 g/L, while calcium hardness was maximum with 69% in most doses and pH ranges. Total nitrogen removal was 30.43% at pH 7 with 0.15 g/L, whereas phosphorous removal was 26.36%.

Table 2 Percentage reduction in physicochemical parameters after treating with ferric chloride

Table 3 depicts the reduction of aquaculture water physicochemical parameters after chitin treatment. Turbidity reduction was observed maximum of 78.2% at pH 8 with a dose of 0.05 g/L. Reduction in electrical conductivity was observed to be poor at pH 6; 12% maximum removal was found to be removal. Chloride reduction was observed to be a maximum of 84.38% at pH 7 with a dose of 0.2 g/Ll. Total hardness removal was going to a maximum of 69.23% at pH 6 with 0.1 g/L, while calcium hardness was maximum at 78.95% at pH 7 with 0.1 g/L. Total nitrogen removal was maximum of 53.04% at pH 7 with 0.2 g/L, and phosphorous removal was 62.72% at pH 8 with 0.05 g/L.

Table 3 Reduction percentage in physicochemical parameters after treating with chitin

Table 4 depicts the reduction of the aquaculture water physicochemical parameters after treatment with seeds of Moringa oleifera. Turbidity reduction was observed maximum of 47.83% at pH 8 with a dose of 0.2 g/L. Reduction in electrical conductivity was observed to be good at pH 8 with around 5.7% removal. The decrease in total solids was negative in all pH and dose ranges. Chloride reduction was observed to be a maximum of 92.71% at pH 7 with a dose of 0.05 g/L. Total hardness removal was negative in all pH and dose ranges, while calcium hardness was maximum with 84.6 2% at pH 7 with amounts 0.1 and 0.2 g/L. Total nitrogen removal was maximum of 50.43% at pH 8 with 0.2 g/L, and phosphorous removal was 69.09% at pH 8 with 0.1 g/L.

Table 4 Percentage reduction in physicochemical parameters after treating with Moringa oleifera seeds (MO)

Table 5 depicts the reduction of the aquaculture water physicochemical parameters after treatment with a blend of seeds of Moringa oleifera and chitin. Turbidity reduction was observed maximum of 56.52% at pH 8 with a dose of 0.05 g/L. Electrical conductivity reduction was observed to be good at pH 8 with around 64.49% and dose 0.1 g/L. Removal of total solids was noted to be 74.00% pH 8 and dose 0.1 g/L. Chloride reduction was observed to be about 93–94% at pH and dose ranges. Total hardness removal was negative, going to be a maximum of 20.14% at pH 7 with 0.1 g/L, while calcium hardness was maximum at 76.92% at pH 8 with 0.05 g/L and 0.1 g/L. Total nitrogen removal was maximum of 81.73% at pH 7 with 0.05 g/L, and phosphorous removal was the highest compared to the other sample’s maximum up to 78%.

Table 5 Percentage reduction in physicochemical parameters after treating with MO + chitin

Parameter-wise comparison between coagulants

Turbidity reduction of aquaculture wastewaters by coagulants was observed to be least with a blended coagulant, which was negative, and highest was observed with ferric chloride coagulant at pH 7 (86.96%) (Fig. 1). Electrical conductivity reduction of aquaculture wastewaters by coagulants was observed to be least with seeds of MO–chitin (0.74%), and highest was observed with ferric chloride at pH 8 (99.81%) (Fig. 2).

Fig. 1
figure 1

Turbidity comparison of the coagulants

Fig. 2
figure 2

Electrical conductivity reduction by the coagulants

Total dissolved solids reduction of aquaculture wastewaters by the coagulant was observed to be least with MO seeds that were negative and highest observed with ferric chloride at pH 8 with all doses (55.98%) (Fig. 3). Chloride reduction of aquaculture wastewaters by the coagulant was observed to be least with ferric chloride (36.46%), and the highest was observed with blended coagulant at all pH and dose ranges (94–95%) (Fig. 4).

Fig. 3
figure 3

Total dissolved solids reduction by the coagulants

Fig. 4
figure 4

Chloride reduction by the coagulants

Total hardness reduction was negative by all the coagulants (Fig. 5) except chitin which was highest with chitin at pH 7, dose 0.15, and 0.20 (84.2%). Calcium hardness reduction of aquaculture wastewaters by the coagulant was observed to be least with chitin, and highest was observed with M. oleifera at pH 7, dose 0.1 and 0.2 (84.6%) (Fig. 6).

Fig. 5
figure 5

Total hardness reduction by the coagulants

Fig. 6
figure 6

Calcium hardness reduction by the coagulants

Total nitrogen reduction of aquaculture wastewaters by the coagulant was observed at least with ferric chloride (18.2) at 7 pH with a dose of 0.1. The highest was observed with MO–chitin at pH 7 with doses 0.05 and 0.15 (Fig. 7). Total phosphorous reduction of aquaculture wastewaters by three coagulants was observed to be least with ferric chloride (16.36%), and the highest was observed with blended coagulant at all pH and dose ranges (70.90–78.18%) (Fig. 8).

Fig. 7
figure 7

Total nitrogen reduction by the coagulants

Fig. 8
figure 8

Total phosphorus reduction by the coagulants

FTIR analysis

FTIR instrument was used to analyze the MO–chitin sample (Fig. 9) near the IR region. The blended powder was strained by 75-µ sieve and mixed with the KBr and compressed and pelletized to a volume of 1/100 W/W and used for the analysis. The adsorption peak for MO–chitin was found at 1373 cm−1 representing C–H of the alkali group with bend structures. The peak at 1586 cm−1 indicated aromatic compounds, and 1646 cm−1 indicated the presence of N–H groups’ bend structures. Further 1703, 1740 cm−1 showed that the samples consisted of carboxylic aldehyde groups are responsible for the adsorption phenomenon—the peaks at 2922 and 3676 cm−1 attributed to the presence of carboxylic and aromatic compounds. The colloidal particles’ adsorption onto the MO–chitin surface is due to the interaction of charges by the hydrogen bonds of carboxylic and alkali groups (Saritha et al. 2019; Araújo et al. 2010; Espíndola-Cortés et al. 2017). The polymer adsorbed might be stabilized or altered depending on the presence of the number of particles and polymers and their affinity toward water–polymer–particles adsorption (Saritha et al. 2019).

Fig. 9
figure 9

FTIR analysis of the coagulant (MO–chitin)

XRD analysis

XRD patterns of the MO–chitin are shown in Fig. 10. The XRD patterns revealed that these materials have amorphous and small crystalline regions (da Silva Lucas et al. 2021; Aleman-Ramirez et al. 2021). XRD patterns explain whether the prepared compounds do not have any impurities and are in pristine forms. In general, the peaks reflect the conditions and effects of the experiments denoting smaller particles size. The MO–chitin offered the reflections in a 2-theta range of 10–90. Intensive peaks are observed at 50.53, 40.83, 38.57, 36.32, 30.44, 28.71, 24.70, and 15.35, indicating the compounds’ crystallinity and amorphous nature. These features might be responsible for the adsorption of pollutants onto the coagulant surface (Aleman-Ramirez et al. 2021).

Fig. 10
figure 10

XRD analysis of the coagulant (MO–chitin)

SEM analysis

SEM analysis of MO–chitin showed (Fig. 11) the firm and dense structure with a heterogeneous and microscopic porous matrix, indicating that all the impurities are adsorbed onto the compound’s surface, which might be attributed to the presence of moieties of proteins. Thus, from these features, it is evident that these compounds have enough morphological profile for adsorbing other impurities.

Fig. 11
figure 11

a Magnified view of MO–chitin at 18 KX. b Magnified view of MO–chitin at 45 KX

Microbial analysis

H2S bottles were used to test the microbial contamination in wastewater, and Fig. 12 shows (a) E. coli, (b) Vibrio, (c) Salmonella in the effluents. However, after treating the sample with MO–chitin coagulants, the microbes were removed entirely from the water samples.

Fig. 12
figure 12

Microbial analysis before treatment (ac) and after treatment (d) with MO–chitin

Discussion

Wastewaters emanating from aquaculture ponds possess typical characteristics like more significant pollutant load in organic matter, nutrients, solids, and salts, causing high turbidity. The turbidity encompasses plankton, clay particles, feces, detritus along with the waste feed. If these solids are removed, recycling these waters is possible. Moreover, as the options for recycling increase, the pollution of water bodies reduces. In these lines, the present study utilized the natural coagulants chitin and seeds of M. oleifera to treat aquaculture wastewaters, compared the efficiency of M. oleifera to that of ferric chloride, and used a blend of coagulants, i.e., MO + Chitin (Moringa oleifera + chitin). The pathway of chitosan coagulation primarily depends on the deacetylation and pH of the wastewater. It has been shown that the greater the deacetylation, the lesser the pH enhanced, which is the performance of chitosan (Wang et al. 2021). Though not in acetylated form, chitin in the present study showed better efficacy in its blended form removing 94–95% of chloride.

50% reduction in TDS was obtained by ferric chloride in the present study. Vijayasri et al. (2013) presented a decrease in COD from initial 102 to final 5.31 mg/L post-treatment with ferric chloride along with the culture of microalgae. This is similar to the results in the present study, where only ferric chloride was not effective in removing pollutant parameters. A noteworthy point was regarding the sturdy flocs formed by ferric coagulant containing Fe (OH)3 with higher density than the flocs created by the organic coagulants in the study (Ebeling et al. 2003).

TDS reduction and turbidity reduction from the aquaculture wastewaters are presented in Figs. 1, and 3, which illustrates the dosage of coagulants governs disparities of TDS and turbidity in wastewaters. The results are in acceptance with the earlier studies (Ebeling et al. 2003). As dosage increased, the TDS and turbidity removal were enhanced by FeCl3 while they diminished swiftly beyond above a dosage of 0.15 g/L for MO and blended coagulant. It is inferred from the results that FeCl3 was much efficient in removing TDS and turbidity from the test waters are due to the reduction of solubility of Fe(OH)3 at high ionic strength (Zhang et al. 2014), results in a lowering the aqueous double-layer thickness among majority solution and floc of the surface (Zhang et al. 2014).

Total hardness is a measure of the concentration of all metal cations except for alkali metals. Much of the concern about hardness in water treatment is with all the ions involved; in aquaculture, the problem is mainly calcium and magnesium concentration. Among various divalent salts, however, calcium and magnesium are understood to be the broader sources of water hardness. Another essential aspect of hardness is its effect on pH—soft water has low pH, and hard water has high pH. A desirable range would be between 75 and 200 mg/L CaCO3. A low level of hardness (10–20 mg/L CaCO3) can cause stress to animals. A high level of hardness is not desirable as it increases the pH and reduces other nutrients’ availability. An essential impact of hardness on aquatic life is the effect of metals as cadmium, lead, chromium, and zinc. The toxicity of these metals decreases with hardness as they form insoluble precipitates and settle at the bottom and become unavailable to the aquatic organisms.

The lower levels of CaCO3 (< 100 mg/L)) hardness present a consistent sign of a lower concentration of calcium. While greater hardness is necessary which may not be due to a greater calcium concentration, it can also be due to high magnesium concentrations with or without calcium. In the current study, the removal of calcium hardness was found to be a maximum of 84.62% by MO. In comparison, overall test coagulants efficiently removed more than 60% of calcium, essential enough for the shrimp growth. Total hardness is a necessary nutrient in shrimp farming—calcium ions minimize the rise of pH during the high photosynthetic rates. These ions are essential for bone formation; the crustaceans’ shell formation in the brackish water aquaculture hardness by calcium ranges from 346 to 896.5 was observed. A review by Aarø (2020) stated that the natural coagulants M. oleifera and chitosan can compete with inorganic coagulants toward water treatment and that both coagulants have a greater affinity toward the removal of pollutants in water which includes organic molecules, inorganic ions through mechanisms like charge neutralization, bridging and electrostatic patch mechanism.

Precisely, while treating aquaculture water with dissolved organic carbon in terms of humic acids, charge neutralization and precipitation are dominant mechanisms of the coagulation process. Metal salts usually have more excellent neutralization capability over organic polymers, and hence, the efficiency of inorganic coagulants for treatment of these wastewaters is supposed to be high (Heiderscheidt et al. 2016; Sillanpää et al. 2018). Moreover, it is understood that the production of insoluble compounds from metal salts tends to improve coagulation/flocculation by enhancing particles’ availability in the suspension, increasing reaction kinetics leading to floc aggregation (Heiderscheidt et al. 2020; Sun et al. 2019).

Heiderscheidt et al. 2020 have reported stable and effective removal of phosphorus from the sludge obtained from aquaculture wastewater using coagulation by inorganic salts. While Zadinelo et al. (2018) said greater efficiency in removing ammonia from aquaculture wastewater upon coagulation with higher doses of chitosan foam, they have attributed to the enhanced surface area and adsorption sites coagulant. Higher concentrations of ammonia in the environment are problematic due to its toxicity, specifically to aquatic organisms, leading to ammonia concentrations and a cascade of intracellular reactions leading to mortality (Haseena et al. 2016). Owing to the biodegradable nature of chitosan and ammonia removed being a nutrient, the sludge obtained can be used as fertilizer.

Effective and faster removal of dissolved orthophosphate was obtained during the interaction of protonates, the chitosan amino groups with phosphate ions in the medium (Zadinelo et al. 2018). The nitrate removal by chitosan foam up to 73% was reported attributed to the foremost mechanism of adsorption by chitosan and physical adsorption (intermolecular) due to van der Waals forces. The adsorption is governed by external factors like temperature, pH, etc. (Zadinelo et al. 2018; Karnena and Saritha 2021). Similar results were obtained by Chung (2006), wherein the concentrations of orthophosphate after treatment were found to be acceptable for discharge into natural waters.

Conclusion

The following conclusions are derived from the present study:

  • Ferric chloride was effective in removing turbidity of the wastewater (86.96%) along with 52.55% of total dissolved solids in all ranges of pH and dose.

  • Chitin proved to be effective in removing turbidity (78.2%), chloride (84%), hardness (84.21%), total nitrogen (53.04%), and total phosphorus (64.84%).

  • Moringa oleifera has effectively reduced chloride to 92.71%, with total nitrogen and total phosphorus removal rates at 50.43% and 69.09%.

  • The di-blend of Moringa oleifera and chitin resulted in a 66.49% reduction in electrical conductivity, 74% reduction in total dissolved solids, 95% reduction of chloride, 81.70% removal of total nitrogen, and 78.18% removal of the total phosphorus.

Overall, di-blend adopted and tested in the study has proved to be promising and very effective in removing various physicochemical parameters that result in causing pollution. Further, the characterization studies carried out on the di-blend coagulant has revealed and proved its coagulation efficacy. FTIR analysis revealed the functional groups that were responsible for the process of coagulation in the di-blend. XRD analysis provided the input of the coagulant being crystalline in nature which would have provided a greater surface area for adsorption. Finally, SEM images have confirmed the sturdy nature of the floc formed on the coagulant. With these observations from the study, it is concluded that natural coagulants are equally competent for the removal of pollution parameters, with blended coagulants offering promising solutions. Hence, further studies will be aimed at the preparation and application of these coagulants at a large scale with possible commercialization.