METHOD FOR PROMOTING THE RAPID PRECIPITATION OF TRAVERTINE CRYSTALS BY ALGAE

Abstract

A method for promoting the rapid precipitation of travertine crystals by algae is disclosed. Microalgae is added to a body of water having a calcium ion concentration of 100-500 mg/L and stirred. The amount of microalgae is 0.1-8?10.sup.8 cells/L. The invention adopts a method for promoting the rapid precipitation of travertine crystals by algae, which significantly improves the sedimentation rate of travertine crystals. At the same time, there are pseudomonas in the calcified water body of algae, which can be used for algae-lysing bacteria isolation and purification.

Claims

1. A method for promoting a rapid precipitation of travertine crystals by an algae comprising adding a microalgae to a body of water having a calcium ion concentration of 100-500 mg/L to obtain a resulting mixture and stirring the resulting mixture, wherein an amount of the microalgae is 0.1-8?10.sup.8 cells/L.

2. The method for promoting the rapid precipitation of the travertine crystals by the algae according to claim 1, wherein a concentration of a magnesium ion in the water is 31.87 mg/L, and a concentration of a bicarbonate ion in the water is 796.8 mg/L.

3. The method for promoting the rapid precipitation of the travertine crystals by the algae according to claim 2, wherein a pH of the water is 7.5.

4. The method for promoting the rapid precipitation of the travertine crystals by the algae according to claim 1, wherein the calcium ion concentration in the water is 300 mg/L.

5. The method for promoting the rapid precipitation of the travertine crystals by the algae according to claim 1, wherein an added quantity of the microalgae is 5.31?10.sup.7 cells/L.

6. The method for promoting the rapid precipitation of the travertine crystals by the algae according to claim 1, wherein the microalgae is at least one selected from the group consisting of Chlorella and diatoms.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0015] FIG. 1 is the X-ray diffraction pattern;

[0016] FIGS. 2A-2C are SEM images of B1, C1, and D1;

[0017] FIGS. 3A-3F are SEM images of D1, D2, D3, D4, D5 and D6;

[0018] FIGS. 4A-4D are SEM images of A6, B6, C6, and D6.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0019] The technical solution of the invention is further explained by drawings and embodiments as follows.

Embodiment 1

[0020] 1) Prepare 5 portions of compound water with a calcium concentration of 100 mg/L.

[0021] 2) Add the Chlorella into the compound water respectively. The adding quantities of Chlorella are 1.98?10.sup.7 cells/L, 5.31?10.sup.7 cells/L, 1.08?10.sup.8 cells/L, 4.86?10.sup.8 cells/L and 7.36?10.sup.8 cells/L, respectively.

[0022] 3) Extract 15 ml water every two days for the detection of Ca.sup.2+ concentration change six times in total.

[0023] 4) Calculate the sedimentation rate of travertine crystals in compound water by the exponential decay equation. The results are shown in Table 1.

TABLE-US-00001 TABLE 1 The sedimentation rate of travertine crystal in compound water when the Ca.sup.2+ concentration is 100 mg/L Ca.sup.2+ initial The adding quantities The sedimentation concentration mg/L of Chlorella mg/L rate mg/L .Math. d 100 1.98 ? 10.sup.7 0.11010 100 5.31 ? 10.sup.7 0.15535 100 1.08 ? 10.sup.8 0.11621 100 4.86 ? 10.sup.8 0.06961 100 7.36 ? 10.sup.8 0.03735

Embodiment 2

[0024] 1) Prepare 5 portions of compound water with a calcium concentration of 300 mg/L.

[0025] 2) Add the Chlorella into the compound water respectively. The adding quantities of Chlorella are 1.98?10.sup.7 cells/L, 5.31?10.sup.7 cells/L, 1.08?10.sup.8 cells/L, 4.86?10.sup.8 cells/L and 7.36?10.sup.8 cells/L, respectively.

[0026] 3) Extract 15 ml water every two days for the detection of Ca.sup.2+ concentration change six times in total.

[0027] 4) Calculate the sedimentation rate of travertine crystals in compound water by the exponential decay equation. The results are shown in Table 2.

TABLE-US-00002 TABLE 2 The sedimentation rate of travertine crystal in compound water when the Ca.sup.2+ concentration is 300 mg/L Ca.sup.2+ initial The adding quantities The sedimentation concentration mg/L of Chlorella mg/L rate mg/L .Math. d 300 1.98 ? 10.sup.7 0.14290 300 5.31 ? 10.sup.7 0.22397 300 1.08 ? 10.sup.8 0.18120 300 4.86 ? 10.sup.8 0.16235 300 7.36 ? 10.sup.8 0.14096

Embodiment 3

[0028] 1) Prepare 5 portions of compound water with a calcium concentration of 500 mg/L.

[0029] 2) Add the Chlorella into the compound water respectively. The adding quantities of Chlorella are 1.98?10.sup.7 cells/L, 5.31?10.sup.7 cells/L, 1.08?10.sup.8 cells/L, 4.86?10.sup.8 cells/L and 7.36?10.sup.8 cells/L, respectively.

[0030] 3) Extract 15 ml water every two days for the detection of Ca.sup.2+ concentration change six times in total.

[0031] 4) Calculate the sedimentation rate of travertine crystals in compound water by the exponential decay equation. The results are shown in Table 3.

TABLE-US-00003 TABLE 3 The sedimentation rate of travertine crystal in compound water when the Ca.sup.2+ concentration is 500 mg/L Ca.sup.2+ initial The adding quantities The sedimentation concentration mg/L of Chlorella mg/L rate mg/L .Math. d 500 1.98 ? 10.sup.7 0.04465 500 5.31 ? 10.sup.7 0.04032 500 1.08 ? 10.sup.8 0.06626 500 4.86 ? 10.sup.8 0.07402 500 7.36 ? 10.sup.8 0.08405

Comparison Case 1

[0032] 1) Prepare 5 portions of compound water with a calcium concentration of 100 mg/L.

[0033] 2) Proceed with the natural sedimentation.

[0034] 3) Extract 15 ml water every two days for the detection of Ca.sup.2+ concentration change six times in total.

[0035] 4) Calculate the sedimentation rate of travertine crystals in compound water by the exponential decay equation. The results are shown in Table 4.

Comparison Case 2

[0036] 1) Prepare 5 portions of compound water with a calcium concentration of 300 mg/L.

[0037] 2) Proceed with the natural sedimentation.

[0038] 3) Extract 15 ml water every two days for the detection of Ca.sup.2+ concentration change six times in total.

[0039] 4) Calculate the sedimentation rate of travertine crystals in compound water by the exponential decay equation. The results are shown in Table 4.

Comparison Case 3

[0040] 1) Prepare 5 portions of compound water with a calcium concentration of 500 mg/L.

[0041] 2) Proceed with the natural sedimentation.

[0042] 3) Extract 15 ml water every two days for the detection of Ca.sup.2+ concentration change six times in total.

[0043] 4) Calculate the sedimentation rate of travertine crystals in compound water by the exponential decay equation. The results are shown in Table 4.

TABLE-US-00004 TABLE 4 The sedimentation rate of travertine crystal in compound water (Comparison cases 1-3) Ca.sup.2+ initial The adding quantities The sedimentation concentration mg/L of Chlorella mg/L rate mg/L .Math. d 100 0 0.03768 300 0 0.05049 500 0 0.01904

The Ca.SUP.2+ Concentration Testing Method

[0044] Extract 15 mL water and measure the Ca.sup.2+ concentration by ICP. The exponential decay equation is used to fit the process of travertine sedimentation. The exponential decay equation is expressed by equation 1, and the exponential decay equation after the logarithm is expressed by equation 2.

[Ca.sup.2+]=e.sup.kt+b(1)

In[Ca.sup.2+]=kt+b(2)

[0045] Where [Ca.sup.2+] represents the calcium ion concentration, t represents the sampling time, k represents the travertine rate constant, d[Ca.sup.2+]/dt represents the travertine rate.

The Travertine Morphology Testing Method

[0046] After 15 days, the deposited travertine crystals in the experiment were detected by XRD and SEM.

The Analysis of Experimental Results

1. The Effect of Different Concentrations of Microalgae on the Calcification Rate: According to the Results of the Sedimentation Rate of Travertine Crystals in Compound Water in Table 1-4,

[0047] When the initial concentration of Ca.sup.2+ is 100.00 mg/L or 300.00 mg/L, the sedimentation rate of travertine crystals was the fastest in the compound water of microalgae solution with the initial concentration of 5.31?10.sup.7 cells/L. When the initial concentration of Ca.sup.2+ was 500.00 mg/L, the calcification rate went faster as the increase of microalgae concentration. The sedimentation rate of travertine crystals in comparison cases 1-3 is significantly lower than that of travertine crystals in embodiments 1-3. At different microalgae concentrations, when the Ca.sup.2+ concentration in the water was 300.00 mg/L, the calcification rate is the fastest.

[0048] Therefore, in low and medium concentrations of Ca.sup.2+ water, the calcification rate is the fastest when the initial concentration of microalgae solution is 5.31?10.sup.7 cells/L. At this time, when the concentration of microalgae increases, the calcification rate decreases instead. In high concentrations of Ca.sup.2+ water, the increase of microalgae concentration will increase the calcification rate. When the concentration of Ca.sup.2+ is about 300.00 mg/L, it is beneficial to increase the sedimentation rate of travertine crystals in water when the concentration of microalgae is about 5.31?10.sup.7 cells/L.

2. The Effect of Microalgae on the Travertine Crystal Structure

[0049] Samples of embodiments 1-3 and comparison cases 1-3 are numbered, as shown in Table 5, and analyzed by XRD. The X-ray diffraction (XRD) cell parameters of travertine sedimentation are shown in table 6.

TABLE-US-00005 TABLE 5 Sample number table Ca.sup.2+ initial Microalgae initial concentration mg/L concentration cells/L No. Comparison case 1 100 0 B1 Comparison case 2 200 0 C1 Comparison case 3 300 0 D1 Embodiment 1 100 1.98 ? 10.sup.7 B2 100 5.31 ? 10.sup.7 B3 100 1.08 ? 10.sup.8 B4 100 4.86 ? 10.sup.8 B5 100 7.36 ? 10.sup.8 B6 Embodiment 2 300 1.98 ? 10.sup.7 C2 300 5.31 ? 10.sup.7 C3 300 1.08 ? 10.sup.8 C4 300 4.86 ? 10.sup.8 C5 300 7.36 ? 10.sup.8 C6 Embodiment 3 500 1.98 ? 10.sup.7 D2 500 5.31 ? 10.sup.7 D3 500 1.08 ? 10.sup.8 D4 500 4.86 ? 10.sup.8 D5 500 7.36 ? 10.sup.8 D6

TABLE-US-00006 TABLE 6 The X-ray diffraction (XRD) cell parameters of travertine sedimentation Group D2 D3 D4 D5 D6 C6 B6 The chemical CaCO.sub.3 CaCO.sub.3 (H.sub.20) formula The crystal Hexagonal, calcite structure The hexagonal system, structure calcite monohydrate structure The space group R-3C(167) p3121 (152) The crystal a/nm 0.49896 0.49896 0.49880 0.49890 0.49890 0.49890 a/nm 0.60931 cell refinement b/nm 0.49896 0.49896 0.49880 0.49890 0.49890 0.49890 b/nm 0.60931 parameters c/nm 1.70610 1.70610 1.70680 1.70620 1.70620 1.70620 c/nm 0.75446 ?/? 90 ?/? 90 ?/? 120 Cell 0.36785 0.36785 0.36776 0.36778 0.36778 0.36778 Cell volume 0.24292 volume/nm.sup.3 Cell 2.71080 2.71080 2.71140 2.71120 2.71120 2.71120 Cell density 2.42530 density(g/cm.sup.3) Number of unit 6 3 cell molecules The main {circle around (1)} (012) 22.9270 23.0510 22.9640 22.9910 23.0500 23.0090 {circle around (1)} (100) 16.7910 advantages {circle around (2)} (104) 29.2400 29.4110 29.3220 29.3200 29.3610 29.3590 {circle around (2)} (101) 20.5280 correspond {circle around (3)} (110) 35.8110 35.9810 35.8930 35.9140 35.9820 35.9560 {circle around (1)} (012) 29.0620 to2?/? {circle around (4)} (113) 39.2590 39.4120 39.3300 39.3430 39.3930 39.3960 {circle around (2)} (111) 31.6220 {circle around (5)} (202) 43.0250 43.1530 43.1060 43.1130 43.1390 43.1490 {circle around (3)} (021) 35.9620 {circle around (6)} (018) 47.3640 47.5110 47.4010 47.3700 47.4030 47.4190 {circle around (4)} (022) 41.7250 {circle around (7)} (116) 48.3650 48.5280 48.4100 48.4290 48.4440 48.4570 {circle around (5)} (211) 47.0260 Cell {circle around (1)} (012) 0.38757 0.38522 0.38695 0.38651 0.38553 0.38622 {circle around (1)} (100) 0.52756 Spacing {circle around (2)} (104) 0.30517 0.30344 0.30434 0.30436 0.30395 0.30397 {circle around (2)} (101) 0.43230 {circle around (3)} (110) 0.25054 0.24940 0.24998 0.24985 0.24939 0.24956 {circle around (3)} (012) 0.30701 {circle around (4)} (113) 0.22929 0.22844 0.22889 0.22882 0.22854 0.22852 {circle around (4)} (111) 0.28270 {circle around (5)} (202) 0.21005 0.20946 0.20968 0.20965 0.20942 0.20948 {circle around (5)} (021) 0.24952 {circle around (6)} (018) 0.19178 0.19121 0.19163 0.19175 0.19163 0.19156 {circle around (6)} (022) 0.21630 {circle around (7)} (116) 0.18804 0.18744 0.18787 0.18780 0.18775 0.18770 {circle around (7)} (211) 0.19307 Grain size {circle around (1)} (012) >100 >100 76.5 86.9 61.7 79.4 {circle around (1)} (100) 59.5 corresponding {circle around (2)} (104) 83.9 89.8 63.3 84.9 49.1 78.6 {circle around (2)} (101) 44.5 to main {circle around (3)} (110) 73.6 >100 >100 >100 53.4 81.5 {circle around (3)} (012) 46.1 advantage {circle around (4)} (113) 69.4 >100 93.6 >100 56.1 97.8 {circle around (4)} (111) 48.2 surface/nm {circle around (5)} (202) >100 >100 >100 >100 52.8 77.5 {circle around (5)} (021) 60.4 {circle around (6)} (018) >100 >100 92.7 89.8 56.4 77.2 {circle around (6)} (022) 45.3 {circle around (7)} (116) >100 >100 >100 79.0 65.2 97.7 {circle around (7)} (211) 29.6 Average grain 68.6 75.4 61.8 71.9 43.2 65.7 Average 25.0 size/nm size/nm

[0050] It can be seen from the unit cell parameter table that in the experimental groups of D2, D3, D4, D5, D6, and C6, the fresh travertine contains the characteristic diffraction peaks of calcite (the main chemical composition is CaCO.sub.3), and the corresponding main advantage surfaces are (012), (104), (110), (113), (202), (018) and (116). The space groups of D2, D3, D4, D5, D6, and C6 are all R-3c (167), the number of unit cell molecules is 6, the 20 corresponding to the main advantage surface is similar, and the cell spacing corresponding to the main advantage surface is not much different. The cell volume is 0.36785 nm.sup.3, 0.36776 nm.sup.3, and 0.36778 nm.sup.3. The cell density is 2.71080 g/cm.sup.3, 2.71120 g/cm.sup.3, and 2.71140 g/cm.sup.3. The average grain size of travertine crystal is less than 100.

[0051] The grain sizes corresponding to the main advantage surfaces of D2, D3, D4, and D5 are partially greater than 100, and the grain sizes corresponding to the main advantage surfaces of D6 and C6 are less than 100.

[0052] The B6 fresh travertine contains calcite characteristic diffraction peaks (the main chemical composition is CaCO.sub.3(H.sub.2O), and the corresponding main advantage surfaces are (100), (101), (012), (111), (021), (022), (211), etc. The B6 space group is P3121 (152), and the number of unit cell molecules is 3. The 20 corresponding to the main advantage surface and the cell spacing corresponding to the main advantage surface are different from those of the D2, D3, D4, D5, D6, and C6 groups. The cell volume is 0.24292 nm.sup.3, the cell density is 2.42530 g/cm.sup.3, and the average grain size of the travertine crystal is 25.0. The grain size corresponding to the main advantage surface of B.sup.6 is less than 100.

[0053] The XRD results show that at the same calcium ion concentration, the travertine crystals produced by different concentrations of microalgae have the same structure as calcite. When the concentration of microalgae increases to 7.36?10.sup.8 cells/L, the cell size of calcite decreases. The results of calcine sedimentation in water with different Ca.sup.2+ concentrations under the same microalgae concentration showed that when the Ca.sup.2+ concentration in the solution decreases to 79.68 mg/L, the structure of calcite will change and may become calcite monohydrate (CaCO.sub.3.Math.H.sub.2O).

3. The Effect of Microalgae on Travertine Crystal Morphology

[0054] By observing the electron microscope images of the blank group without microalgae solution under different Ca.sup.2+ concentrations (as shown in FIGS. 2A-2C):

[0055] When Ca.sup.2+ is 100.00 mg/L, the calcite travertine is observed, but at this time, it is mainly in small crystal travertine form with a small amount of standard calcite.

[0056] When Ca.sup.2+ concentration increases to 300.00 mg/L, the proportion of small crystal travertine increases.

[0057] When the concentration of Ca.sup.2+ increases to 500.00 mg/L, the size of small crystal travertine increases, and filamentous algae imprinting is observed.

[0058] Comparing the D2-D6 experimental groups with different microalgae concentrations at the same calcium ion concentration (500.00 mg/mL), it was found that when the microalgae concentration increases, the shape of the formed travertine will be closer to the standard and mature calcite, and at the same time, due to the high concentration of microalgae, its dead body was covered on the surface of the travertine crystal, resulting in only a very small amount of travertine seen in the electron microscope picture. In the case of low-concentration microalgae, more travertine crystals can be observed by scanning electron microscope. However, other salt crystals appeared in the lowest concentration of microalgae solution.

[0059] By observing the electron microscope images of the experimental groups with different Ca.sup.2+ concentrations under the same microalgae concentration (as shown in FIGS. 3A-3F), it was found that the blank group (A6) with Ca.sup.2+ equals to 0 had no travertine crystals, only the other salt crystals appeared. The electron microscopy images of the experimental group showed that with the increase of calcium ion concentration, the travertine crystals developed more mature, and the travertine crystal contour became clear (calcite with unclear contour-petal shape calcite-hexagonal calcite).

[0060] By observing all samples (FIGS. 2A-2C, 3A-3F, and 4A-4D), it can be found that the travertine sedimentation is based on the pores of microalgae. The travertine produced by microalgae produces microalgae accumulation first, then the travertine is generated based on microalgae accumulation, and then the microalgae accumulation covers the travertine. This process will occur repeatedly in the process of microalgae sedimentation. This phenomenon is the crystal core of microalgae calcic sedimentation.

[0061] In summary, this method can be used to repair travertine in degraded or damaged areas of the travertine landscape by cultivating microalgae.

[0062] Finally, it should be noted that the above embodiments are only used to explain the technical solution of the invention rather than to limit it. Although the invention is described in detail with references to the better embodiments, ordinary technicians in this field should understand that they can still modify or replace the technical solution of the invention, and these modifications or equivalent replacements cannot make the modified technical solution out of the spirit and scope of the technical solution of the invention.