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In-situ  synthesis of zinc oxide modified graphitic carbon nitride composite ( in-situ  ZnO-g-C 3 N 4 ) was carried out  via a  one-step thermal condensation method where [ZnCl 2 .2{HONC(CH 3 ) 2 }] was used as a precursor for zinc oxide while urea was taken as a source of g-C 3 N 4 . In another synthesis process, urea was also decomposed with ZnO nanoparticles to yield ZnO-g-C 3 N 4  composite and urea alone decomposed to g-C 3 N 4 . The  in-situ  ZnO-g-C 3 N 4  has a higher surface area, 128.68 m 2 /g as compared to ZnO-g-C 3 N 4  (88.99 m 2 /g) and g-C 3 N 4  (87.22 m 2  /g). The enhanced photocatalytic activity performance of materials against MB  i.e.   in-situ  ZnO-g-C 3 N 4 , 99.37%; ZnO-g-C 3 N 4 , 97.02% and g-C 3 N 4 , 92.12% degradation within 90 minutes in sunlight. The adsorption capacities towards Pb 2+ , Cd 2+  and Cr 3+  heavy metal ions on  in-situ  ZnO-g-C 3 N 4  is 48.144 mg.g -1 , 48.883 mg.g -1  and 40.108 mg.g -1 ; on ZnO-g-C 3 N 4  is 43.043 mg.g -1 , 45.005 mg.g -1  and 37.766 mg g -1 ;and ong-C 3 N 4  is 39.057 mg.g -1 , 41.495 mg.g -1  and33.855 mg.g -1 .

In-situ synthesis of ZnO modified g-C 3 N 4 composite: a potential photocatalyst and adsorbent for waste water remediation